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Sample records for facile combustion synthesis

  1. Facile combustion synthesis of novel CaZrO 3

    Indian Academy of Sciences (India)

    Abstract. A facile sol–gel combustion route was reported for the direct preparation of CaZrO3:Eu3+ and CaZrO3:Eu3+, Gd3+. The obtained deposits were characterized by XRD, TGA-DSC, SEM, EDS, PL measurements and microscope fluorescence. When the Gd3+ ions were introduced in this compound, the emissions of ...

  2. High Combustion Research Facility

    Data.gov (United States)

    Federal Laboratory Consortium — At NETL's High-Pressure Combustion Research Facility in Morgantown, WV, researchers can investigate new high-pressure, high-temperature hydrogen turbine combustion...

  3. Facile combustion synthesis of ZnO nanoparticles using Cajanus cajan (L.) and its multidisciplinary applications

    Energy Technology Data Exchange (ETDEWEB)

    Manjunath, K.; Ravishankar, T.N. [Centre for Nano and Material Sciences, Jain University, Jakkasandra, Kanakapura Talluk (India); Kumar, Dhanith [Department of Chemistry, B.M.S. Instsitute of Technology, Yelahanka, Bangalore (India); Priyanka, K.P; Varghese, Thomas [Nanoscience Research Centre, Department of Physics, Nirmala College, Muvattupuzha, Kerala (India); Naika, H.Raja [Department of Studies and Research in Environmental Science, Tumkur University, Tumkur (India); Nagabhushana, H. [CNR Rao Center for Advanced Materials, Tumkur University, Tumkur (India); Sharma, S.C. [Chattisgarh Swami Vivekananda Technical University, Bhilai (India); Dupont, J. [Institute of Chemistry, Laboratory of Molecular Catalysis, UFRGS, Porto Alegre (Brazil); Ramakrishnappa, T. [Centre for Nano and Material Sciences, Jain University, Jakkasandra, Kanakapura Talluk (India); Nagaraju, G., E-mail: nagarajugn@rediffmail.com [Department of Chemistry, B.M.S. Instsitute of Technology, Yelahanka, Bangalore (India)

    2014-09-15

    Graphical abstract: Facile combustion synthesis of ZnO nanoparticles using Cajanuscajan (L.) and its multidisciplinary applications.Zinc oxide nanoparticles were successfully synthesized by solution combustion method (SCM) using pigeon pea as a combustible fuel for the first time. The as-prepared product shows good photocatalytic, dielectric, antibacterial, electrochemical properties. - Highlights: • ZnO Nps were synthesized via combustion method using pigeon pea as a fuel. • The structure of the product was confirmed by XRD technique. • The morphology was confirmed by SEM and TEM images. • The as-prepared product shown good photocatalytic activity, dielectric property. • It has also shown good antibacterial and electrochemical properties. - Abstract: Zinc oxide nanoparticles (ZnO Nps) were successfully synthesized by solution combustion method (SCM) using pigeon pea as a fuel for the first time. X-Ray diffraction pattern reveals that the product belongs to hexagonal system. FTIR spectrum of ZnO Nps shows the band at 420 cm{sup −1} associated with the characteristic vibration of Zn–O. TEM images show that the nanoparticles are found to be ∼40–80 nm. Furthermore, the as-prepared ZnO Nps exhibits good photocatalytic activity for the photodegradation of methylene blue (MB), indicating that they are indeed a promising photocatalytic semiconductor. The antibacterial properties of ZnO nanopowders were investigated by their bactericidal activity against four bacterial strains.

  4. Facile combustion synthesis of ZnO nanoparticles using Cajanus cajan (L.) and its multidisciplinary applications

    International Nuclear Information System (INIS)

    Manjunath, K.; Ravishankar, T.N.; Kumar, Dhanith; Priyanka, K.P; Varghese, Thomas; Naika, H.Raja; Nagabhushana, H.; Sharma, S.C.; Dupont, J.; Ramakrishnappa, T.; Nagaraju, G.

    2014-01-01

    Graphical abstract: Facile combustion synthesis of ZnO nanoparticles using Cajanuscajan (L.) and its multidisciplinary applications.Zinc oxide nanoparticles were successfully synthesized by solution combustion method (SCM) using pigeon pea as a combustible fuel for the first time. The as-prepared product shows good photocatalytic, dielectric, antibacterial, electrochemical properties. - Highlights: • ZnO Nps were synthesized via combustion method using pigeon pea as a fuel. • The structure of the product was confirmed by XRD technique. • The morphology was confirmed by SEM and TEM images. • The as-prepared product shown good photocatalytic activity, dielectric property. • It has also shown good antibacterial and electrochemical properties. - Abstract: Zinc oxide nanoparticles (ZnO Nps) were successfully synthesized by solution combustion method (SCM) using pigeon pea as a fuel for the first time. X-Ray diffraction pattern reveals that the product belongs to hexagonal system. FTIR spectrum of ZnO Nps shows the band at 420 cm −1 associated with the characteristic vibration of Zn–O. TEM images show that the nanoparticles are found to be ∼40–80 nm. Furthermore, the as-prepared ZnO Nps exhibits good photocatalytic activity for the photodegradation of methylene blue (MB), indicating that they are indeed a promising photocatalytic semiconductor. The antibacterial properties of ZnO nanopowders were investigated by their bactericidal activity against four bacterial strains

  5. Combustion Research Facility

    Data.gov (United States)

    Federal Laboratory Consortium — For more than 30 years The Combustion Research Facility (CRF) has served as a national and international leader in combustion science and technology. The need for a...

  6. Combustion Research Facility | A Department of Energy Office of Science

    Science.gov (United States)

    Collaborative Research Facility Back to Sandia National Laboratory Homepage Combustion Research Search the CRF Combustion Chemistry Flame Chemistry Research.Combustion_Chemistry.Flame_Chemistry Theory and Modeling Theory and Modeling Combustion Kinetics High Pressure Chemistry Chemistry of Autoignition

  7. Processing of hydroxyapatite obtained by combustion synthesis

    International Nuclear Information System (INIS)

    Canillas, M.; Rivero, R.; García-Carrodeguas, R.; Barba, F.; Rodríguez, M.A.

    2017-01-01

    One of the reasons of implants failure are the stress forces appearing in the material–tissue interface due to the differences between their mechanical properties. For this reason, similar mechanical properties to the surrounding tissue are desirable. The synthesis of hydroxyapatite by solution combustion method and its processing have been studied in order to obtain fully dense ceramic bodies with improved mechanical strength. Combustion synthesis provides nanostructured powders characterized by a high surface area to facilitate the following sintering. Moreover, synthesis was conducted in aqueous and oxidizing media. Oxidizing media improve homogenization and increase the energy released during combustion. It gives rise to particles whose morphology and size suggest lower surface energies compared with aqueous media. The obtained powders were sintered by using a controlled sintering rate schedule. Lower surfaces energies minimize the shrinkage during sintering and relative densities measurements and diametral compression test confirm improved densification and consequently mechanical properties. [es

  8. Processing of hydroxyapatite obtained by combustion synthesis

    Directory of Open Access Journals (Sweden)

    M. Canillas

    2017-09-01

    Full Text Available One of the reasons of implants failure are the stress forces appearing in the material–tissue interface due to the differences between their mechanical properties. For this reason, similar mechanical properties to the surrounding tissue are desirable. The synthesis of hydroxyapatite by solution combustion method and its processing have been studied in order to obtain fully dense ceramic bodies with improved mechanical strength. Combustion synthesis provides nanostructured powders characterized by a high surface area to facilitate the following sintering. Moreover, synthesis was conducted in aqueous and oxidizing media. Oxidizing media improve homogenization and increase the energy released during combustion. It gives rise to particles whose morphology and size suggest lower surface energies compared with aqueous media. The obtained powders were sintered by using a controlled sintering rate schedule. Lower surfaces energies minimize the shrinkage during sintering and relative densities measurements and diametral compression test confirm improved densification and consequently mechanical properties.

  9. Combustion synthesis and preliminary luminescence studies of ...

    Indian Academy of Sciences (India)

    The polycrystalline sample of LiBaPO4 : Tb3+ (LBPT) was successfully synthesized by solution combustion synthesis and studied for its luminescence characteristics. The thermoluminescence (TL) glow curve of LBPT material consists of two peaks at 204.54 and 251.21°C. The optimum concentration was 0.005 mol to ...

  10. The solution combustion synthesis of nanophosphors

    Energy Technology Data Exchange (ETDEWEB)

    Tornga, Stephanie C [Los Alamos National Laboratory

    2009-01-01

    Nanophosphors are defined as nano-sized (1-100mn), insulating, inorganic materials that emit light under particle or electromagnetic excitation. Their unique luminescence properties provide an excellent potential for applications in radiation detection and imaging. Herein, solution combustion synthesis (SCS) is presented as a method to prepare nanophosphor powders, while X-ray diffraction (XRD), transmission electron microscopy (TEM), photoluminescence (PL), photoluminescence excitation (PLE), and other techniques were used to characterize their structural and optical properties. The goal of this work is to synthesize bright, high-quality powders of nanophosphors, consolidate them into bulk materials and study their structural and optical properties using XRD, TEM, PL, and PLE. SCS is of interest because it is a robust, inexpensive, and facile technique, which yields a significant amount of a wide variety of oxide materials, in a short amount of time. Several practical nanophosphors were synthesized and investigated in this work, including simple oxides such as Y{sub 2}O{sub 3}:Bi, Y{sub 2}O{sub 3}:Tb, Y{sub 2}O{sub 3}:Eu and Gd{sub 2}O{sub 3}:Eu, complex oxides such as Gd{sub 2}SiO{sub 5}:Ce, Y{sub 2}SiO{sub 5}:Ce, Lu{sub 2}SiO{sub 5}:Ce, Zn{sub 2}SiO{sub 4}:Mn, and Y{sub 3}Al{sub 5}O{sub 12}:Ce. Results demonstrate that altering the processing parameters such as water content of the precursor solution, ignition temperature, fuel type and amount, and post-synthesis annealing can significantly improve light output, and that it is possible to optimize the luminescence output of oxyorthosilicates by reducing the amount of silica in the precursor mixture.

  11. Facile and rapid auto-combustion synthesis of nano-porous γ-Al2O3 by application of hexamethylenetetramine in fuel composition

    Science.gov (United States)

    Salem, Shiva; Salem, Amin; Parni, Mohammad Hosein; Jafarizad, Abbas

    2018-06-01

    In this article, urea, glycine and hexamethylenetetramine were blended in accordance with the mixture design algorithm to prepare γ-Al2O3 by auto-combustion technique. Aluminum nitrate was then mixed with the stoichiometric contents of prepared fuel solutions to obtain gel systems. The gels exhibited a typical self-propagating combustion behavior at low temperature, directly resulting amorphous materials. The precursors were calcined at various temperatures ranging from 700 to 900 °C. The treated powders were evaluated by determining the methylene blue (MB) adsorption efficiency. The production condition to obtain γ-Al2O3 with maximum surface area depends on fuel composition and calcination temperature. The alumina powder fabricated by this procedure was uniformly distributed and contains nano-sized secondary particles with diameter about 10-30 nm in which the average pore size is 3.2 nm induced large surface area, 240 m2g-1. The employment of hexamethylenetetramine provides a potential for synthesis of γ-Al2O3 at lower temperature, 700 °C, with maximum MB removal efficiency.

  12. Combustion synthesis and structural characterization of Li–Ti mixed

    Indian Academy of Sciences (India)

    Combustion synthesis and structural characterization of Li–Ti mixed nanoferrites ... were prepared by combustion method at lower temperatures compared to the ... first time at low temperatures, using PEG which acts as a new fuel and oxidant.

  13. Combustion synthesis and structural characterization of Li–Ti mixed ...

    Indian Academy of Sciences (India)

    pared by combustion method at lower temperatures compared to the conventional high temperature sintering for ... Li–Ti mixed ferrites; combustion synthesis; hysteresis. 1. ... Quantum model - VSM 6000) at an applied field of ±10 kOe.

  14. Synthesis of functional materials in combustion reactions

    Science.gov (United States)

    Zhuravlev, V. D.; Bamburov, V. G.; Ermakova, L. V.; Lobachevskaya, N. I.

    2015-12-01

    The conditions for obtaining oxide compounds in combustion reactions of nitrates of metals with organic chelating-reducing agents such as amino acids, urea, and polyvinyl alcohol are reviewed. Changing the nature of internal fuels and the reducing agent-to-oxidizing agent ratio makes possible to modify the thermal regime of the process, fractal dimensionality, morphology, and dispersion of synthesized functional materials. This method can be used to synthesize simple and complex oxides, composites, and metal powders, as well as ceramics and coatings. The possibilities of synthesis in combustion reactions are illustrated by examples of αand γ-Al2O3, YSZ composites, uranium oxides, nickel powder, NiO and NiO: YSZ composite, TiO2, and manganites, cobaltites, and aluminates of rare earth elements.

  15. Production of nanocrystalline metal powders via combustion reaction synthesis

    Science.gov (United States)

    Frye, John G.; Weil, Kenneth Scott; Lavender, Curt A.; Kim, Jin Yong

    2017-10-31

    Nanocrystalline metal powders comprising tungsten, molybdenum, rhenium and/or niobium can be synthesized using a combustion reaction. Methods for synthesizing the nanocrystalline metal powders are characterized by forming a combustion synthesis solution by dissolving in water an oxidizer, a fuel, and a base-soluble, ammonium precursor of tungsten, molybdenum, rhenium, or niobium in amounts that yield a stoichiometric burn when combusted. The combustion synthesis solution is then heated to a temperature sufficient to substantially remove water and to initiate a self-sustaining combustion reaction. The resulting powder can be subsequently reduced to metal form by heating in a reducing gas environment.

  16. Combustion synthesis of inorganic materials; Muki zairyo no nensho gose

    Energy Technology Data Exchange (ETDEWEB)

    Oyanagi, M. [Ryukoku University, Kyoto (Japan)

    1999-11-01

    Combustion synthesis of porous titan carbide is outlined. In combustion synthesis, exothermic chain reaction, which is induced by igniting at one point of the simple substance mixture, propagates the combustion wave, and the compound is synthesized, which can be sintered by it. By this method, to this day intermetallic compounds, ceramics and high melting point composite materials have been synthesized, and synthetics can be made compact by adding pressure during or just after the reaction. Recently, applying the induction heating jointly, preheating before the reaction and heat treatment after the reaction can be controlled, accordingly, many high melting point inorganic compounds and composite materials can be made by combustion synthesis under pressure. (NEDO)

  17. HERCULES Advanced Combustion Concepts Test Facility: Spray/Combustion Chamber

    Energy Technology Data Exchange (ETDEWEB)

    Herrmann, K. [Eidgenoessische Technische Hochschule (ETH), Labor fuer Aerothermochemie und Verbrennungssysteme, Zuerich (Switzerland)

    2004-07-01

    This yearly report for 2004 on behalf of the Swiss Federal Office of Energy (SFOE) at the Laboratory for Aero-thermochemistry and Combustion Systems at the Federal Institute of Technology ETH in Zurich, Switzerland, presents a review of work being done within the framework of HERCULES (High Efficiency R and D on Combustion with Ultra Low Emissions for Ships) - the international R and D project concerning new technologies for ships' diesels. The work involves the use and augmentation of simulation models. These are to be validated using experimental data. The report deals with the development of an experimental set-up that will simulate combustion in large two-stroke diesel engines and allow the generation of reference data. The main element of the test apparatus is a spray / combustion chamber with extensive possibilities for optical observation under variable flow conditions. The results of first simulations confirm concepts and shall help in further work on the project. The potential offered by high-speed camera systems was tested using the institute's existing HTDZ combustion chamber. Further work to be done is reviewed.

  18. Direct Connect Supersonic Combustion Facility (Research Cell 22)

    Data.gov (United States)

    Federal Laboratory Consortium — Description: RC22 is a continuous-flow, direct-connect supersonic-combustion research facility that is capable of simulating flight conditions from Mach 3.0 to Mach...

  19. High temperature combustion facility: present capabilities and future prospects

    International Nuclear Information System (INIS)

    Boccio, J.L.; Ginsberg, T.; Ciccarelli, G.

    1995-01-01

    The high-temperature combustion facility constructed and operated by the Department of Advanced Technology of Brookhaven National Laboratory to support and promote research in the area of hydrogen combustion phenomena in mixtures prototypical to light-water reactor containment atmospheres under potential severe accident conditions is reported. The facility can accommodate combustion research activities encompassing the fields of detonation physics, flame acceleration, and low-speed deflagration in a wide range of combustible gas mixtures at initial temperatures up to 700 K and post-combustion pressures up to 100 atmospheres. Some preliminary test results are presented that provide further evidence that the effect of temperature is to increase the sensitivity of hydrogen-air-steam mixtures to undergo detonation [ru

  20. Gel combustion synthesis of yttria stabilized zirconia

    International Nuclear Information System (INIS)

    Vijay, Soja K.; Chandramouli, V.; Anthonysamy, S.

    2013-01-01

    Nano - crystalline 8 mol% yttria stabilized zirconia (YSZ) powders were synthesized by gel combustion technique employing both microwave heating as well as conventional heating method. Three different fuels - citric acid, urea and glycine were used for the synthesis with fuel to oxidant ratio as 1:1. The effect of fuel on the crystal structure, particle size, specific surface area, morphology and sintering density was studied. X-ray powder diffraction (XRD), BET gas adsorption technique, dynamic light scattering, transmission and scanning electron microscopy (TEM and SEM) and micro-Raman spectroscopy were used to characterize the powders. The results obtained for powders obtained using both methods - microwave assisted and hotplate - were compared. The specific surface area of powders in all cases are comparable except in the case of urea as fuel where microwave assisted synthesis yielded powders with lower surface area. The particle size distribution of all samples obtained using microwave method was unimodal, whereas the particle size distribution of samples prepared using hot plate method using urea fuel showed bimodal distribution. The compacts obtained using powders with citric acid and glycine as fuel showed more than 94% theoretical density, whereas the samples obtained using urea showed density below 90% of theoretical density. (author)

  1. Combustion Synthesis of Nanomaterials Using Various Flame Configurations

    KAUST Repository

    Ismail, Mohamed

    2016-01-01

    Titanium dioxide (TiO2) is an important semiconducting metal oxide and is expected to play an important role in future applications related to photonic crystals, energy storage, and photocatalysis. Two aspects regarding the combustion synthesis have

  2. Synthesis of nanocrystalline Gd doped ceria by combustion technique

    DEFF Research Database (Denmark)

    Jadhav, L. D.; Chourashiya, M. G.; Subhedar, K. M.

    2009-01-01

    chemical method of combustion where in the combustion of precursors results in the formation of nanoparticles relatively at lower processing temperature. The thermogravimetric study was carried out to understand the ignition temperature and optimize the fuel-to-oxidant ratio. The successful synthesis...

  3. Combustion synthesis of boride and other composites

    International Nuclear Information System (INIS)

    Halverson, D.C.; Lum, B.Y.; Munir, Z.A.

    1989-01-01

    This patent describes a self-sustaining combustion synthesis process for producing hard, tough, lightweight B 4 C/TiB 2 composites. It is based on the thermodynamic dependence of adiabatic temperature and product composition on the stoichiometry of the B 4 C and TiB 2 reactants. For lightweight products the composition must be relatively rich in the B 4 C component. B 4 C-rich composites are obtained by varying the initial temperature of the reactants. The product is hard, porous material whose toughness can be enhanced by filling the pores with aluminum or other metal phases using a liquid metal infiltration process. The process can be extended to the formation of other composites having a low exothermic component.0:008360his patent describes a neutron reactivity control system for a LWBR incorporating a stationary seed-blanket core arrangement. The core arrangement includes a plurality of contiguous hexagonal shaped regions. Each region has a central and a peripheral blanket area juxapositioned an annular seed area. The blanket areas contain thoria fuel rods while the annular seed area includes seed fuel rods and movable thoria shim control rods

  4. High Pressure Combustion Experimental Facility(HPCEF) for Studies on Combustion in Reactive Flows

    Science.gov (United States)

    2017-12-13

    SECURITY CLASSIFICATION OF: 1. REPORT DATE (DD-MM-YYYY) 4. TITLE AND SUBTITLE 13. SUPPLEMENTARY NOTES 12. DISTRIBUTION AVAILIBILITY STATEMENT 6...Report: High Pressure Combustion Experimental Facility (HPCEF) for Studies on Combustion in Reactive Flows The views, opinions and/or findings... contained in this report are those of the author(s) and should not contrued as an official Department of the Army position, policy or decision, unless so

  5. Combustion

    CERN Document Server

    Glassman, Irvin

    1997-01-01

    This Third Edition of Glassman's classic text clearly defines the role of chemistry, physics, and fluid mechanics as applied to the complex topic of combustion. Glassman's insightful introductory text emphasizes underlying physical and chemical principles, and encompasses engine technology, fire safety, materials synthesis, detonation phenomena, hydrocarbon fuel oxidation mechanisms, and environmental considerations. Combustion has been rewritten to integrate the text, figures, and appendixes, detailing available combustion codes, making it not only an excellent introductory text but also an important reference source for professionals in the field. Key Features * Explains complex combustion phenomena with physical insight rather than extensive mathematics * Clarifies postulates in the text using extensive computational results in figures * Lists modern combustion programs indicating usage and availability * Relates combustion concepts to practical applications.

  6. Combustion Synthesis Of Ultralow-density Nanoporous Gold Foams

    Energy Technology Data Exchange (ETDEWEB)

    Tappan, Bruce C [Los Alamos National Laboratory; Mueller, Alex H [Los Alamos National Laboratory; Steiner, Stephen A [Los Alamos National Laboratory; Luther, Erik P [Los Alamos National Laboratory

    2008-01-01

    A new synthetic pathway for producing nanoporous gold monoliths through combustion synthesis from Au bistetrazoJeamine complexes has been demonstrated. Applications of interest for Au nanofoams include new substrates for nanoparticle-mediated catalysis, embedded antennas, and spectroscopy. Integrated support-and-catalystin-one nanocomposites prepared through combustion synthesis of mixed AuBTA/metal oxide pellets would also be an interesting technology approach for low-cost in-line catalytic conversion media. Furthermore, we envision preparation of ultrahigh surface area gold electrodes for application in electrochemical devices through this method.

  7. Internal Combustion Engine Powered by Synthesis Gas from Pyrolysed Plastics

    Directory of Open Access Journals (Sweden)

    Chríbik Andrej

    2016-07-01

    Full Text Available The article discusses the application of synthesis gas from pyrolysis of plastics in petrol engine. The appropriate experimental measurements were performed on a combustion engine LGW 702 designated for micro-cogeneration unit. The power parameters, economic parameters in term of brake specific fuel consumption, and internal parameters of the engine were compared to the engine running on the reference fuel - natural gas and synthesis gas. Burning synthesis gas leads to decreased performance by about 5% and to increased mass hourly consumption by 120 %. In terms of burning, synthesis gas has similar properties as natural gas. Compared with [5] a more detailed study has been prepared on the effects of angle of spark advance on the engine torque, giving more detailed assessment of engine cycle variability and considering specification of start and end of combustion in the logarithm p-V diagram.

  8. Combustion Dynamics Facility: April 1990 workshop working group reports

    Energy Technology Data Exchange (ETDEWEB)

    Kung, A.H.; Lee, Y.T.

    1990-04-01

    This document summarizes results from a workshop held April 5--7, 1990, on the proposed Combustion Dynamics Facility (CDF). The workshop was hosted by the Lawrence Berkeley Laboratory (LBL) and Sandia National Laboratories (SNL) to provide an opportunity for potential users to learn about the proposed experimental and computational facilities, to discuss the science that could be conducted with such facilities, and to offer suggestions as to how the specifications and design of the proposed facilities might be further refined to address the most visionary scientific opportunities. Some 130 chemical physicists, combustion chemists, and specialists in UV synchrotron radiation sources and free-electron lasers (more than half of whom were from institutions other than LBL and SNL) attended the five plenary sessions and participated in one or more of the nine parallel working group sessions. Seven of these sessions were devoted to broadening and strengthening the scope of CDF scientific opportunities and to detail the experimental facilities required to realize these opportunities. Two technical working group sessions addressed the design and proposed performance of two of the major CDF experimental facilities. These working groups and their chairpersons are listed below. A full listing of the attendees of the workshop is given in Appendix A. 1 tab.

  9. Modelling of flame temperature of solution combustion synthesis of ...

    Indian Academy of Sciences (India)

    Administrator

    The basis of combustion synthesis technique comes from the ... of oxidizer to fuel is calculated using the total oxidizing ..... +. −. ∑. (4) where S/Nm is the mean S/N ratio of all the experimental ..... Minitab Inc., User manual of MINITAB. TM.

  10. Combustion synthesis of graphene and ultracapacitor performance

    Indian Academy of Sciences (India)

    Graphene sheets are synthesized by a simple method starting from graphitic oxide as a precursor. Reaction of graphitic oxide at 250 °C with a combustion mixture of urea and ammonium nitrate results in the formation of thin graphene sheets. Graphene formation is characterized by XRD, TGA, XPS and TEM. Graphene ...

  11. Safety analysis of the 700-horsepower combustion test facility

    Energy Technology Data Exchange (ETDEWEB)

    Berkey, B.D.

    1981-05-01

    The objective of the program reported herein was to provide a Safety Analysis of the 700 h.p. Combustion Test Facility located in Building 93 at the Pittsburgh Energy Technology Center. Extensive safety related measures have been incorporated into the design, construction, and operation of the Combustion Test Facility. These include: nitrogen addition to the coal storage bin, slurry hopper, roller mill and pulverizer baghouse, use of low oxygen content combustion gas for coal conveying, an oxygen analyzer for the combustion gas, insulation on hot surfaces, proper classification of electrical equipment, process monitoring instrumentation and a planned remote television monitoring system. Analysis of the system considering these factors has resulted in the determination of overall probabilities of occurrence of hazards as shown in Table I. Implementation of the recommendations in this report will reduce these probabilities as indicated. The identified hazards include coal dust ignition by hot ductwork and equipment, loss of inerting within the coal conveying system leading to a coal dust fire, and ignition of hydrocarbon vapors or spilled oil, or slurry. The possibility of self-heating of coal was investigated. Implementation of the recommendations in this report will reduce the ignition probability to no more than 1 x 10/sup -6/ per event. In addition to fire and explosion hazards, there are potential exposures to materials which have been identified as hazardous to personal health, such as carbon monoxide, coal dust, hydrocarbon vapors, and oxygen deficient atmosphere, but past monitoring experience has not revealed any problem areas. The major environmental hazard is an oil spill. The facility has a comprehensive spill control plan.

  12. Auto-combustion Synthesis, Characterization and Photovoltaic

    African Journals Online (AJOL)

    NICOLAAS

    Ag-NiTiO3, sol-gel method, semiconductor, photovoltaic, doping. 1. Introduction ... convenient for synthesis of pure mixed metal oxides nanoparticles. Furthermore .... current density voltage (I-V) curve for Ag-NiTiO3 was carried out under the ...

  13. Combustion synthesis and characterization of uranium and thorium tellurides

    International Nuclear Information System (INIS)

    Czechowicz, D.G.

    1985-10-01

    This report describes an investigation of the chemical systems uranium-tellurium and thorium-tellurium. A novel synthesis technique, combustion synthesis, which uses the exothermic heat of reaction rather than externally supplied heat, was utilized to form the phases UTe, U 3 Te 4 , and UTe 2 in the U-Te system and the phases ThTe, Th 2 Te 3 , and ThTe 2 in the Th-Te system from reactions of the type U/sub x/ + Te/sub y/ = U/sub x/Te/sub y/. With this synthetic method, U-Te and Th-Te products could be formed in a matter of seconds, and the purity of the products was often greater than that of the starting materials used. Control over final product stoichiometry was found to be very difficult. The product phase distribution observed in combustion products, as determined by x-ray diffraction, electron microprobe, and optical metallographic methods, was found to be spatially complex. Lattice constants were calculated from x-ray diffraction patterns for the compounds UTe, U 3 Te 4 , and ThTe. SOLGASMIX thermodynamic equilibrium calculations were performed using available and estimated thermodynamic data on the system U-Te-O in an attempt to understand the products formed by combustion. Adiabatic combustion reaction temperatures for specific U-Te and Th-Te reactions were also calculated utilizing available and estimated thermodynamic data. 71 refs., 31 figs., 15 tabs

  14. Cermet materials prepared by combustion synthesis and metal infiltration

    Science.gov (United States)

    Holt, Joseph B.; Dunmead, Stephen D.; Halverson, Danny C.; Landingham, Richard L.

    1991-01-01

    Ceramic-metal composites (cermets) are made by a combination of self-propagating high temperature combustion synthesis and molten metal infiltration. Solid-gas, solid-solid and solid-liquid reactions of a powder compact produce a porous ceramic body which is infiltrated by molten metal to produce a composite body of higher density. AlN-Al and many other materials can be produced.

  15. Combustion synthesis of LaFeO3 sensing nanomaterial

    International Nuclear Information System (INIS)

    Zaza, F.; Serra, E.; Pallozzi, V.; Pasquali, M.

    2014-01-01

    Since industrial revolution, human activities drive towards unsustainable global economy due to the overexploitation of natural resources and the unacceptable emissions of pollution and greenhouse gases. In order to address that issue, engineering research has been focusing on gas sensors development for monitoring gas emissions and controlling the combustion process sustainability. Semiconductors metal oxides sensors are attractive technology because they require simple design and fabrication, involving high accessibility, small size and low cost. Perovskite oxides are the most promising sensing materials because sensitivity, selectivity, stability and speed-response can be modulated and optimized by changing the chemical composition. One of the most convenient synthesis process of perovskite is the citrate-nitrate auto-combustion method, in which nitrate is the oxidizing agent and citrate is the fuel and the chelating argent in the same time. Since the sensibility of perovskite oxides depends on the defective crystallographic structure and the nanomorphology, the experimental was designed in order to study the dependence of powder properties on the synthesis conditions, such as the solution acidity and the relative amount of metals, nitrates and citric acid. Crystalline structure was studied in depth for defining the effects of synthesis conditions on size, morphology and crystallographic structure of nanopowders of LaFeO 3

  16. The Multi-User Droplet Combustion Apparatus: the Development and Integration Concept for Droplet Combustion Payloads in the Fluids and Combustion Facility Combustion Integrated Rack

    Science.gov (United States)

    Myhre, C. A.

    2002-01-01

    The Multi-user Droplet Combustion Apparatus (MDCA) is a multi-user facility designed to accommodate four different droplet combustion science experiments. The MDCA will conduct experiments using the Combustion Integrated Rack (CIR) of the NASA Glenn Research Center's Fluids and Combustion Facility (FCF). The payload is planned for the International Space Station. The MDCA, in conjunction with the CIR, will allow for cost effective extended access to the microgravity environment, not possible on previous space flights. It is currently in the Engineering Model build phase with a planned flight launch with CIR in 2004. This paper provides an overview of the capabilities and development status of the MDCA. The MDCA contains the hardware and software required to conduct unique droplet combustion experiments in space. It consists of a Chamber Insert Assembly, an Avionics Package, and a multiple array of diagnostics. Its modular approach permits on-orbit changes for accommodating different fuels, fuel flow rates, soot sampling mechanisms, and varying droplet support and translation mechanisms to accommodate multiple investigations. Unique diagnostic measurement capabilities for each investigation are also provided. Additional hardware provided by the CIR facility includes the structural support, a combustion chamber, utilities for the avionics and diagnostic packages, and the fuel mixing capability for PI specific combustion chamber environments. Common diagnostics provided by the CIR will also be utilized by the MDCA. Single combustible fuel droplets of varying sizes, freely deployed or supported by a tether are planned for study using the MDCA. Such research supports how liquid-fuel-droplets ignite, spread, and extinguish under quiescent microgravity conditions. This understanding will help us develop more efficient energy production and propulsion systems on Earth and in space, deal better with combustion generated pollution, and address fire hazards associated with

  17. Combustion synthesis of ceramic matrices for immobilization of 14C

    International Nuclear Information System (INIS)

    Bosc-Rouessac, F.; Marin-Ayral, R.M.; Haidoux, A.; Massoni, N.; Bart, F.

    2008-01-01

    In this study, the use of combustion synthesis for immobilization of 14 C was considered. Ceramic matrices have been prepared by this method using two different devices: one non-conventional with preheating of the samples and the other conventional device where ignition was produced thanks to tungsten filament. These two devices gave rise to different mechanisms of reactions involving different amounts of unreacted carbon graphite inside the matrix. The SHS samples were characterized by using scanning electron microscopy (SEM) and X-ray diffraction (XRD)

  18. Solution combustion synthesis and characterization of nanosized bismuth ferrite

    Science.gov (United States)

    Sai Kumar, V. Sesha; Rao, K. Venkateswara; Krishnaveni, T.; Kishore Goud, A. Shiva; Reddy, P. Ranjith

    2012-06-01

    The present paper describes a simple method of nanosized BiFeO3 by the solution combustion synthesis using bismuth and iron nitrates as oxidizers and the combination fuel of citric acid and ammonium hydroxide, with fuel to oxidizer ratio (Ψ = 1) one. The X-ray Diffraction results indicated rhombohedral phase (R3m) with JCPDS data card no: 72-2035. The ferroelectric transition of the sample at 8310C was detected by differential thermal analysis. Thermal analysis was done by Thermal gravimetric-Differential thermal analyzer and obtained results were presented in this paper.

  19. A new combustion route to γ-Fe2O3 synthesis

    Indian Academy of Sciences (India)

    A new combustion route for the synthesis of -Fe2O3 is reported by employing purified -Fe2O3 as aprecursor in the present investigation. This synthesis which is similar to a self propagation combustion reaction, involves fewer steps, a shorter overall processing time, is a low energy reaction without the need of any ...

  20. Combustible gas concentration control facility and operation method therefor

    International Nuclear Information System (INIS)

    Yoshikawa, Kazuhiro; Ando, Koji; Kinoshita, Shoichiro; Yamanari, Shozo; Moriya, Kimiaki; Karasawa, Hidetoshi

    1998-01-01

    The present invention provides a hydrogen gas-control facility by using a fuel battery-type combustible gas concentration reducing device as a countermeasure for controlling a hydrogen gas in a reactor container. Namely, a hydrogen electrode adsorb hydrogen by using an ion exchange membrane comprising hydrogen ions as a charge carrier. An air electrode adsorb oxygen in the air. A fuel battery converts recombining energy of hydrogen and oxygen to electric energy. Hydrogen in this case is supplied from an atmosphere in the container. Oxygen in this case is supplied from the air outside of the container. If hydrogen gas should be generated in the reactor, power generation of is performed by the fuel battery by using hydrogen gas, as a fuel, on the side of the hydrogen electrode of the fuel battery and using oxygen, as a fuel, in the air outside of the container on the side of the air electrode. Then, the hydrogen gas is consumed thereby controlling the hydrogen gas concentration in the container. Electric current generated in the fuel battery is used as an emergency power source for the countermeasure for a severe accident. (I.S.)

  1. Combustible gas concentration control facility and operation method therefor

    Energy Technology Data Exchange (ETDEWEB)

    Yoshikawa, Kazuhiro; Ando, Koji; Kinoshita, Shoichiro; Yamanari, Shozo; Moriya, Kimiaki; Karasawa, Hidetoshi

    1998-09-25

    The present invention provides a hydrogen gas-control facility by using a fuel battery-type combustible gas concentration reducing device as a countermeasure for controlling a hydrogen gas in a reactor container. Namely, a hydrogen electrode adsorb hydrogen by using an ion exchange membrane comprising hydrogen ions as a charge carrier. An air electrode adsorb oxygen in the air. A fuel battery converts recombining energy of hydrogen and oxygen to electric energy. Hydrogen in this case is supplied from an atmosphere in the container. Oxygen in this case is supplied from the air outside of the container. If hydrogen gas should be generated in the reactor, power generation of is performed by the fuel battery by using hydrogen gas, as a fuel, on the side of the hydrogen electrode of the fuel battery and using oxygen, as a fuel, in the air outside of the container on the side of the air electrode. Then, the hydrogen gas is consumed thereby controlling the hydrogen gas concentration in the container. Electric current generated in the fuel battery is used as an emergency power source for the countermeasure for a severe accident. (I.S.)

  2. Sub-scale Direct Connect Supersonic Combustion Facility (Research Cell 18)

    Data.gov (United States)

    Federal Laboratory Consortium — Description: RC18 is a continuous-flow, direct-connect, supersonic-combustion research facility that is capable of simulating flight conditions from Mach 3.0 to Mach...

  3. Thermoluminescence properties of zinc oxide obtained by solution combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Orante B, V. R.; Escobar O, F. M.; Cruz V, C. [Universidad de Sonora, Departamento de Investigacion en Polimeros y Materiales, Apdo. Postal 130, 83000 Hermosillo, Sonora (Mexico); Bernal, R., E-mail: victor.orante@polimeros.uson.mx [Universidad de Sonora, Departamento de Investigacion en Fisica, Apdo. Postal 5-088, 83190 Hermosillo, Sonora (Mexico)

    2014-08-15

    High-dose thermoluminescence dosimetry properties of novel zinc oxide obtained by solution combustion synthesis in a glycine-nitrate process, with a non-stoichiometric value of the elemental stoichiometric coefficient (Φ{sub c}) are presented in this work. Zn O powder samples obtained were annealed afterwards at 900 grades C during 2 h in air. Sintered particles of sizes between ∼ 0.5 and ∼ 2 μm were obtained, according to scanning electron microscopy results. X-ray diffraction indicates the presence of the hexagonal phase of Zn O for the powder samples obtained, before and after thermal annealing, without any remaining nitrate peaks observed. Thermoluminescence glow curves of Zn O obtained after being exposed to beta radiation consists of two maxima; one located at ∼ 149 grades C and another at ∼ 308 grades C, being the latter the dosimetric component of the curve. Dosimetric characterization of non-stoichiometric zinc oxide provided experimental evidence like asymptotic behavior of the Tl signal fading for times greater than 16 h between irradiation and the corresponding Tl readout, as well as the linear behaviour of the dose response without saturation in the dose interval studied (from 12.5 up to 400 Gy). Such characteristics place Zn O phosphors obtained in this work as a promising material for high-dose radiation dosimetry applications (e.g., radiotherapy and food industry). (author)

  4. Thermoluminescence properties of zinc oxide obtained by solution combustion synthesis

    International Nuclear Information System (INIS)

    Orante B, V. R.; Escobar O, F. M.; Cruz V, C.; Bernal, R.

    2014-08-01

    High-dose thermoluminescence dosimetry properties of novel zinc oxide obtained by solution combustion synthesis in a glycine-nitrate process, with a non-stoichiometric value of the elemental stoichiometric coefficient (Φ c ) are presented in this work. Zn O powder samples obtained were annealed afterwards at 900 grades C during 2 h in air. Sintered particles of sizes between ∼ 0.5 and ∼ 2 μm were obtained, according to scanning electron microscopy results. X-ray diffraction indicates the presence of the hexagonal phase of Zn O for the powder samples obtained, before and after thermal annealing, without any remaining nitrate peaks observed. Thermoluminescence glow curves of Zn O obtained after being exposed to beta radiation consists of two maxima; one located at ∼ 149 grades C and another at ∼ 308 grades C, being the latter the dosimetric component of the curve. Dosimetric characterization of non-stoichiometric zinc oxide provided experimental evidence like asymptotic behavior of the Tl signal fading for times greater than 16 h between irradiation and the corresponding Tl readout, as well as the linear behaviour of the dose response without saturation in the dose interval studied (from 12.5 up to 400 Gy). Such characteristics place Zn O phosphors obtained in this work as a promising material for high-dose radiation dosimetry applications (e.g., radiotherapy and food industry). (author)

  5. Mechanochemical and combustion synthesis of CeB{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Akguen, Baris [Roketsan Missiles Inc., Ankara (Turkey); Sevinc, Naci; Topkaya, Yavuz [Middle East Technical Univ., Ankara (Turkey). Dept. of Metallurgical and Materials Engineerung; Camurlu, H. Erdem [Akdeniz Univ., Antalya (Turkey). Dept. of Mechanical Engineering

    2013-04-15

    CeB{sub 6} powder was prepared via combustion synthesis (CS) and mechanochemical processing (MCP) methods starting from CeO{sub 2}, B{sub 2}O{sub 3} and Mg powder mixtures. In CS, reactant mixtures were ignited in a preheated pot furnace under argon atmosphere. Products contained CeB{sub 6}, MgO and Mg{sub 3}B{sub 2}O{sub 6}, as revealed by X-ray diffraction analysis. After leaching in 1 M HCl for 15h, MgO was removed but Mg{sub 3}B{sub 2}O{sub 6} could not be removed from the products. Ball milling of products in ethanol prior to leaching made the removal of Mg{sub 3}B{sub 2}O{sub 6} possible by leaching. Yield of CeB{sub 6} was 68.6% in CS. MCP was performed in a stainless steel vial with a planetary ball mill at 300 rpm for 30h. MCP products contained CeB{sub 6}, MgO and small amount of Fe. Leaching in 1 M HCl for 30min was sufficient to remove MgO. Yield of CeB{sub 6} was 84.4% in MCP. According to scanning electron microscopy examinations, particles of CeB6 prepared by CS and MCP had submicrometer size. Average particle sizes were determined as 290nm and 240nm, respectively.

  6. Combustion synthesis of TiB2-based cermets: modeling and experimental results

    International Nuclear Information System (INIS)

    Martinez Pacheco, M.; Bouma, R.H.B.; Katgerman, L.

    2008-01-01

    TiB 2 -based cermets are prepared by combustion synthesis followed by a pressing stage in a granulate medium. Products obtained by combustion synthesis are characterized by a large remaining porosity (typically 50%). To produce dense cermets, a subsequent densification step is performed after the combustion process and when the reacted material is still hot. To design the process, numerical simulations are carried out and compared to experimental results. In addition, physical and electrical properties of the products related to electrical contact applications are evaluated. (orig.)

  7. Numerical investigation of high temperature synthesis gas premixed combustion via ANSYS Fluent

    Directory of Open Access Journals (Sweden)

    Pashchenko Dmitry

    2018-01-01

    Full Text Available A numerical model of the synthesis gas pre-mixed combustion is developed. The research was carried out via ANSYS Fluent software. Verification of the numerical results was carried out using experimental data. A visual comparison of the flame contours that obtained by the synthesis gas combustion for Re = 600; 800; 1000 was performed. A comparison of the wall temperature of the combustion chamber, obtained with the help of the developed model, with the results of a physical experiment was also presented. For all cases, good convergence of the results is observed. It is established that a change in the temperature of the syngas/air mixture at the inlet to the combustion chamber does not significantly affect the temperature of the combustion products due to the dissipation of the H2O and CO2 molecules. The obtained results are of practical importance for the design of heat engineering plants with thermochemical heat recovery.

  8. Using Combustion Synthesis to Reinforce Berms and Other Regolith Structures

    Science.gov (United States)

    Rodriquez, Gary

    2013-01-01

    The Moonraker Excavator and other tools under development for use on the Moon, Mars, and asteroids will be employed to construct a number of civil engineering projects and to mine the soil. Mounds of loose soil will be subject to the local transport mechanisms plus artificial mechanisms such as blast effects from landers and erosion from surface vehicles. Some of these structures will require some permanence, with a minimum of maintenance and upkeep. Combustion Synthesis (CS) is a family of processes and techniques whereby chemistry is used to transform materials, often creating flame in a hard vacuum. CS can be used to stabilize civil engineering works such as berms, habitat shielding, ramps, pads, roadways, and the like. The method is to unroll thin sheets of CS fabric between layers of regolith and then fire the fabric, creating a continuous sheet of crusty material to be interposed among layers of loose regolith. The combination of low-energy processes, ISRU (in situ resource utilization) excavator, and CS fabrics, seems compelling as a general method for establishing structures of some permanence and utility, especially in the role of robotic missions as precursors to manned exploration and settlement. In robotic precursory missions, excavator/ mobility ensembles mine the Lunar surface, erect constructions of soil, and dispense sheets of CS fabrics that are covered with layers of soil, fired, and then again covered with layers of soil, iterating until the desired dimensions and forms are achieved. At the base of each berm, for example, is a shallow trench lined with CS fabric, fired and filled, mounded, and then covered and fired, iteratively to provide a footing against lateral shear. A larger trench is host to a habitat module, backfilled, covered with fabric, covered with soil, and fired. Covering the applied CS fabric with layers of soil before firing allows the resulting matrix to incorporate soil both above and below the fabric ply into the fused layer

  9. Manufacturing Demonstration Facility: Low Temperature Materials Synthesis

    International Nuclear Information System (INIS)

    Graham, David E.; Moon, Ji-Won; Armstrong, Beth L.; Datskos, Panos G.; Duty, Chad E.; Gresback, Ryan; Ivanov, Ilia N.; Jacobs, Christopher B.; Jellison, Gerald Earle; Jang, Gyoung Gug; Joshi, Pooran C.; Jung, Hyunsung; Meyer, Harry M.; Phelps, Tommy

    2015-01-01

    The Manufacturing Demonstration Facility (MDF) low temperature materials synthesis project was established to demonstrate a scalable and sustainable process to produce nanoparticles (NPs) for advanced manufacturing. Previous methods to chemically synthesize NPs typically required expensive, high-purity inorganic chemical reagents, organic solvents and high temperatures. These processes were typically applied at small laboratory scales at yields sufficient for NP characterization, but insufficient to support roll-to-roll processing efforts or device fabrication. The new NanoFermentation processes described here operated at a low temperature (~60 C) in low-cost, aqueous media using bacteria that produce extracellular NPs with controlled size and elemental stoichiometry. Up-scaling activities successfully demonstrated high NP yields and quality in a 900-L pilot-scale reactor, establishing this NanoFermentation process as a competitive biomanufacturing strategy to produce NPs for advanced manufacturing of power electronics, solid-state lighting and sensors.

  10. Facile Synthesis of Ternary Boron Carbonitride Nanotubes

    Directory of Open Access Journals (Sweden)

    Luo Lijie

    2009-01-01

    Full Text Available Abstract In this study, a novel and facile approach for the synthesis of ternary boron carbonitride (B–C–N nanotubes was reported. Growth occurred by heating simple starting materials of boron powder, zinc oxide powder, and ethanol absolute at 1150 °C under a mixture gas flow of nitrogen and hydrogen. As substrate, commercial stainless steel foil with a typical thickness of 0.05 mm played an additional role of catalyst during the growth of nanotubes. The nanotubes were characterized by SEM, TEM, EDX, and EELS. The results indicate that the synthesized B–C–N nanotubes exhibit a bamboo-like morphology and B, C, and N elements are homogeneously distributed in the nanotubes. A catalyzed vapor–liquid–solid (VLS mechanism was proposed for the growth of the nanotubes.

  11. Manufacturing Demonstration Facility: Low Temperature Materials Synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Graham, David E. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Moon, Ji-Won [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Armstrong, Beth L. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Datskos, Panos G. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Duty, Chad E. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Gresback, Ryan [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Ivanov, Ilia N. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jacobs, Christopher B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jellison, Gerald Earle [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jang, Gyoung Gug [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Joshi, Pooran C. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jung, Hyunsung [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Meyer, III, Harry M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Phelps, Tommy [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2015-06-30

    The Manufacturing Demonstration Facility (MDF) low temperature materials synthesis project was established to demonstrate a scalable and sustainable process to produce nanoparticles (NPs) for advanced manufacturing. Previous methods to chemically synthesize NPs typically required expensive, high-purity inorganic chemical reagents, organic solvents and high temperatures. These processes were typically applied at small laboratory scales at yields sufficient for NP characterization, but insufficient to support roll-to-roll processing efforts or device fabrication. The new NanoFermentation processes described here operated at a low temperature (~60 C) in low-cost, aqueous media using bacteria that produce extracellular NPs with controlled size and elemental stoichiometry. Up-scaling activities successfully demonstrated high NP yields and quality in a 900-L pilot-scale reactor, establishing this NanoFermentation process as a competitive biomanufacturing strategy to produce NPs for advanced manufacturing of power electronics, solid-state lighting and sensors.

  12. Microscope-Based Fluid Physics Experiments in the Fluids and Combustion Facility on ISS

    Science.gov (United States)

    Doherty, Michael P.; Motil, Susan M.; Snead, John H.; Malarik, Diane C.

    2000-01-01

    At the NASA Glenn Research Center, the Microgravity Science Program is planning to conduct a large number of experiments on the International Space Station in both the Fluid Physics and Combustion Science disciplines, and is developing flight experiment hardware for use within the International Space Station's Fluids and Combustion Facility. Four fluids physics experiments that require an optical microscope will be sequentially conducted within a subrack payload to the Fluids Integrated Rack of the Fluids and Combustion Facility called the Light Microscopy Module, which will provide the containment, changeout, and diagnostic capabilities to perform the experiments. The Light Microscopy Module is planned as a fully remotely controllable on-orbit microscope facility, allowing flexible scheduling and control of experiments within International Space Station resources. This paper will focus on the four microscope-based experiments, specifically, their objectives and the sample cell and instrument hardware to accommodate their requirements.

  13. Combustion

    CERN Document Server

    Glassman, Irvin

    1987-01-01

    Combustion, Second Edition focuses on the underlying principles of combustion and covers topics ranging from chemical thermodynamics and flame temperatures to chemical kinetics, detonation, ignition, and oxidation characteristics of fuels. Diffusion flames, flame phenomena in premixed combustible gases, and combustion of nonvolatile fuels are also discussed. This book consists of nine chapters and begins by introducing the reader to heats of reaction and formation, free energy and the equilibrium constants, and flame temperature calculations. The next chapter explores the rates of reactio

  14. Combustion Synthesis of Nanomaterials Using Various Flame Configurations

    KAUST Repository

    Ismail, Mohamed Anwar

    2016-02-01

    Titanium dioxide (TiO2) is an important semiconducting metal oxide and is expected to play an important role in future applications related to photonic crystals, energy storage, and photocatalysis. Two aspects regarding the combustion synthesis have been investigated; scale-up in laboratory synthesis and advanced nanoparticle synthesis. Concerning the scale-up issue, a novel curved wall-jet (CWJ) burner was designed for flame synthesis. This was achieved by injecting precursors of TiO2 through a central port into different flames zones that were stabilized by supplying fuel/air mixtures as an annular-inward jet over the curved wall. This provides a rapid mixing of precursors in the reaction zone with hot products. In order to increase the contact surface between the precursor and reactants as well as its residence time within the hot products, we proposed two different modifications. The CWJ burner was modified by adding a poppet valve on top of the central port to deliver the precursor tangentially into the recirculating flow upstream within the recirculation zone. Another modification was made by adopting double-slit curved wall-jet (DS-CWJ) configuration, one for the reacting mixture and the other for the precursor instead of the central port. Particle growth of titanium dioxide (TiO2) nanoparticles and their phases were investigated. Ethylene (C2H4), propane (C3H8), and methane (CH4) were used with varying equivalence ratio and Reynolds number and titanium tetraisopropoxide (TTIP) was the precursor. Flow field and flame structure were quantified using particle image velocimetry (PIV) and OH planar laser-induced fluorescence (PLIF) techniques, respectively. TiO2 nanoparticles were characterized using high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Raman Spectroscopy, and BET nitrogen adsorption for surface area analysis. The flow field quantified by PIV consisted of a wall-jet region leading to a recirculation zone, an

  15. Gas-Phase Combustion Synthesis of Aluminum Nitride Powder

    Science.gov (United States)

    Axelbaum, R. L.; Lottes, C. R.; Huertas, J. I.; Rosen, L. J.

    1996-01-01

    Due to its combined properties of high electrical resistivity and high thermal conductivity aluminum nitride (AlN) is a highly desirable material for electronics applications. Methods are being sought for synthesis of unagglomerated, nanometer-sized powders of this material, prepared in such a way that they can be consolidated into solid compacts having minimal oxygen content. A procedure for synthesizing these powders through gas-phase combustion is described. This novel approach involves reacting AlCl3, NH3, and Na vapors. Equilibrium thermodynamic calculations show that 100% yields can be obtained for these reactants with the products being AlN, NaCl, and H2. The NaCl by-product is used to coat the AlN particles in situ. The coating allows for control of AlN agglomeration and protects the powders from hydrolysis during post-flame handling. On the basis of thermodynamic and kinetic considerations, two different approaches were employed to produce the powder, in co-flow diffusion flame configurations. In the first approach, the three reactants were supplied in separate streams. In the second, the AlCl3 and NH3 were premixed with HCl and then reacted with Na vapor. X-ray diffraction (XRD) spectra of as-produced powders show only NaCl for the first case and NaCl and AlN for the second. After annealing at 775 C tinder dynamic vacuum, the salt was removed and XRD spectra of powders from both approaches show only AlN. Aluminum metal was also produced in the co-flow flame by reacting AlCl3 with Na. XRD spectra of as-produced powders show the products to be only NaCl and elemental aluminum.

  16. Combustion

    CERN Document Server

    Glassman, Irvin

    2008-01-01

    Combustion Engineering, a topic generally taught at the upper undergraduate and graduate level in most mechanical engineering programs, and many chemical engineering programs, is the study of rapid energy and mass transfer usually through the common physical phenomena of flame oxidation. It covers the physics and chemistry of this process and the engineering applications-from the generation of power such as the internal combustion automobile engine to the gas turbine engine. Renewed concerns about energy efficiency and fuel costs, along with continued concerns over toxic and particulate emissions have kept the interest in this vital area of engineering high and brought about new developments in both fundamental knowledge of flame and combustion physics as well as new technologies for flame and fuel control. *New chapter on new combustion concepts and technologies, including discussion on nanotechnology as related to combustion, as well as microgravity combustion, microcombustion, and catalytic combustion-all ...

  17. Combustible gas recombining method and processing facility for gas waste

    International Nuclear Information System (INIS)

    Watabe, Atsushi; Murakami, Kazuo

    1998-01-01

    Combustible gases (hydrogen, oxygen) generated by radiation decomposition of reactor water in the vicinity of a reactor core in a reactor pressure vessel of a BWR type nuclear power plant pass, together with flow of steams, through a gas/water separator and a steam dryer disposed at the upper portion of a reactor core. A catalyst for allowing hydrogen and oxygen to react efficiently and recombine them into water is plated on the surface of the steam dryer. The catalyst comprises palladium (Pd) or platinum (Pt) or a Pd-Pt alloy. The combustible gases passing through the steam dryer are recombined and formed into steams by the catalyst. A slight amount of hydrogen and oxygen which are not recombined transfers, together with main steams, from a main steam pipe to a main condensator by way of a turbine. Then they are released, together with air from an air extraction device, from an activated carbon-type rare gas hold up tower. (I.N.)

  18. Survey of current trends in DNA synthesis core facilities.

    Science.gov (United States)

    Hager, K M; Fox, J W; Gunthorpe, M; Lilley, K S; Yeung, A

    1999-12-01

    The Nucleic Acids Research Group of the Association of Biomolecular Resource Facilities (ABRF) last surveyed DNA synthesis core facilities in April 1995. Because of the introduction of new technologies and dramatic changes in the market, we sought to update survey information and to determine how academic facilities responded to the challenge presented by commercial counterparts. The online survey was opened in January 1999 by notifying members and subscribers to the ABRF electronic discussion group. The survey consisted of five parts: general facility information, oligonucleotide production profile, oligonucleotide charges, synthesis protocols, and trends in DNA synthesis (including individual comments). All submitted data were anonymously coded. Respondents from DNA synthesis facilities were primarily from the academic category and were established between 1984 and 1991. Typically, a facility provides additional services such as DNA sequencing and has upgraded to electronic ordering. There is stability in staffing profiles for these facilities in that the total number of employees is relatively unchanged, the tenure for staff averages 5.9 years, and experience is extensive. On average, academic facilities annually produce approximately 1/16 the number of oligonucleotides produced by the average commercial facilities, but all facilities report an increase in demand. Charges for standard oligonucleotides from academic facilities are relatively higher than from commercial companies; however, the opposite is true for modified phosphoramidites. Subsidized facilities charge less than nonsubsidized facilities. Synthesis protocols and reagents are standard across the categories. Most facilities offer typical modifications such as biotinylation. Despite the competition by large commercial facilities that have reduced costs dramatically, academic facilities remain a stable entity. Academic facilities enhance the quality of service by focusing on nonstandard

  19. Oxy-Combustion Burner and Integrated Pollutant Removal Research and Development Test Facility

    Energy Technology Data Exchange (ETDEWEB)

    Mark Schoenfield; Manny Menendez; Thomas Ochs; Rigel Woodside; Danylo Oryshchyn

    2012-09-30

    A high flame temperature oxy-combustion test facility consisting of a 5 MWe equivalent test boiler facility and 20 KWe equivalent IPR® was constructed at the Hammond, Indiana manufacturing site. The test facility was operated natural gas and coal fuels and parametric studies were performed to determine the optimal performance conditions and generated the necessary technical data required to demonstrate the technologies are viable for technical and economic scale-up. Flame temperatures between 4930-6120F were achieved with high flame temperature oxy-natural gas combustion depending on whether additional recirculated flue gases are added to balance the heat transfer. For high flame temperature oxy-coal combustion, flame temperatures in excess of 4500F were achieved and demonstrated to be consistent with computational fluid dynamic modeling of the burner system. The project demonstrated feasibility and effectiveness of the Jupiter Oxygen high flame temperature oxy-combustion process with Integrated Pollutant Removal process for CCS and CCUS. With these technologies total parasitic power requirements for both oxygen production and carbon capture currently are in the range of 20% of the gross power output. The Jupiter Oxygen high flame temperature oxy-combustion process has been demonstrated at a Technology Readiness Level of 6 and is ready for commencement of a demonstration project.

  20. Combustion synthesis: A new approach for preparation of thermoelectric zinc antimonide compounds

    Energy Technology Data Exchange (ETDEWEB)

    Rouessac, F., E-mail: Florence.Rouessac@univ-montp2.fr [Institut Charles Gerhardt Montpellier, UMR 5253 CNRS-UM2-ENSCM-UM1, C2M Universite Montpellier 2, CC 1504 Place Eugene Bataillon, 34095 Montpellier Cedex 5 (France); Ayral, R.-M. [Institut Charles Gerhardt Montpellier, UMR 5253 CNRS-UM2-ENSCM-UM1, C2M Universite Montpellier 2, CC 1504 Place Eugene Bataillon, 34095 Montpellier Cedex 5 (France)

    2012-07-25

    Highlights: Black-Right-Pointing-Pointer Reliable preparation method of thermoelectric materials. Black-Right-Pointing-Pointer Formation of zinc antimonide by the combustion synthesis method is investigated. Black-Right-Pointing-Pointer XRD and Raman spectroscopy as a function of temperature. Black-Right-Pointing-Pointer SHS: a new way for synthesizing thermoelectric materials. - Abstract: Due to the interesting properties of Zn{sub 4}Sb{sub 3} thermoelectric material, a reliable preparation method of this material is required. In this study, the formation of zinc antimonides by the combustion synthesis method is investigated and subjected to characterization using X-ray diffraction and Raman spectroscopy as a function of temperature. The results show that combustion synthesis can be a new way for synthesizing these thermoelectric materials.

  1. Combustion synthesis of advanced materials. [using in-situ infiltration technique

    Science.gov (United States)

    Moore, J. J.; Feng, H. J.; Perkins, N.; Readey, D. W.

    1992-01-01

    The combustion synthesis of ceramic-metal composites using an in-situ liquid infiltration technique is described. The effect of varying the reactants and their stoichiometry to provide a range of reactant and product species i.e. solids, liquids and gases, with varying physical properties e.g. thermal conductivity, on the microstructure and morphology of synthesized products is also described. Alternatively, conducting the combustion synthesis reaction in a reactive gas environment is also discussed, in which advantages can be gained from the synergistic effects of combustion synthesis and vapor phase transport. In each case, the effect of the presence or absence of gravity (density) driven fluid flow and vapor transport is discussed as is the potential for producing new and perhaps unique materials by conducting these SHS reactions under microgravity conditions.

  2. Synthesis and characterization of reactions by nanoferrites Co2Fe2O4 combustion

    International Nuclear Information System (INIS)

    Santos, P.T.A.; Dantas, B.B.; Costa, A.C.F.M.; Araujo, P.M.A.G.

    2012-01-01

    In this work CoFe 2 O 4 of magnetic nanoparticles were synthesized by combustion reaction and the structural and morphological characteristics of the synthesized samples as well as the parameters of synthesis temperature and reaction time were investigated in order to assess the reproducibility of the synthesis. The maximum temperature and time of the combustion flame were obtained with pyrometer coupled to a computer with online measurement and a stopwatch. The resulting samples were characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The maximum temperature achieved during synthesis for all reactions ranged from 623 deg C and 755 deg C. The combustion flame time varied between 18 and 23 seconds. The XRD showed the formation of only CoFe 2 O 4 inverse spinel phase, with crystallite size 28 nm and crystallinity 78%, with typical morphology of the formation of agglomerates of uniform size, brittle and comprising nanoparticles together by weak forces. (author)

  3. Fast Reacting Nano Composite Energetic Materials: Synthesis and Combustion Characterization

    Science.gov (United States)

    2015-08-24

    nanoenergetic composites finding extensive use in ordnance and industrial applications, because of its high heat of combustion (~32 kJ/g) (S. H. Fischer ...2011. Farley, Cory. "Reactions of Aluminum with Halogen Containing Oxides." Dissertation. Lubbock, TX, May 2013. Gesner, Jeff , Michelle Pantoya, and...characteristics of novel hybrid nanoenergetic formulations." Combustion and Flame 158 (2011): 964- 978. S. H. Fischer , M. C. Grubelich. "Theoretical

  4. MnO/N–C anode materials for lithium-ion batteries prepared by cotton-templated combustion synthesis

    Directory of Open Access Journals (Sweden)

    Cheng-Gong Han

    2017-10-01

    Full Text Available We herein report a facile one-pot synthesis of MnO/N-doped carbon (N–C composites via a sustainable cotton-template glycine–nitrate combustion synthesis to yield superior anode materials for Li ion batteries. MnO nanoparticles with several nanometers were well-embedded in a porous N-doped carbon matrix. It displays the unique characteristics, including the shortened Li+-ion transport path, increased contact areas with the electrolyte solution, inhibited volume changes and agglomeration of nanoparticles, as well as good conductivity and structural stability during the cycling process, thereby benefiting the superior cycling performance and rate capability. This favorable electrochemical performance of obtained MnO/N–C composites via a one-pot biomass-templated glycine/nitrate combustion synthesis renders the suitability as anode materials for Li-ion batteries. Keywords: Biomass, Cotton, Manganese oxide, Lithium ion battery, Porous carbon

  5. In situ synthesis of NiAl–NbB2 composite powder through combustion synthesis

    International Nuclear Information System (INIS)

    Shokati, Ali Akbar; Parvin, Nader; Sabzianpour, Naser; Shokati, Mohammad; Hemmati, Ali

    2013-01-01

    Highlights: ► A Novel NiAl matrix composite powder with 0–40 wt.% NbB 2 was synthesized. ► Composite powders were synthesized by thermal explosion reaction of Ni–Al–Nb–B system. ► Microhardness of NiAl considerably increased with raising NbB 2 content. ► Synthesized composite powders is a good candidate as precursor for thermal barrier application. - Abstract: Synthesis of a novel NiAl matrix composite powder reinforced with 0–40 wt.% NbB 2 by combustion synthesis in thermal explosion mode was investigated. The elemental powders of Ni, Al, Nb, and amorphous boron were used as starting material. For all compositions final products consisted of only the NiAl and NbB 2 phases. Coarser NbB 2 with a relatively uniform distribution in NiAl matrix was formed with rising NbB 2 content. Microhardness of NiAl considerably increased from 377 ± 13 HV 0.05 to 866 ± 81 HV 0.05 for NiAl with 40 wt.% NbB 2 . High microhardness, proper size and distribution of NbB 2 in NiAl matrix make it a good candidate as precursor for thermal spray application.

  6. All-acrylic superelastomers: facile synthesis and exceptional mechanical behavior

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Wei; Goodwin, Andrew; Wang, Yangyang; Yin, Panchao; Wang, Weiyu; Zhu, Jiahua; Wu, Ting; Lu, Xinyi; Hu, Bin; Hong, Kunlun; Kang, Nam-Goo; Mays, Jimmy (Tennessee-K); (ORNL)

    2018-01-01

    All-acrylic multigraft copolymers made by a facile synthesis procedure exhibit elongation at break >1700% and strain recovery behavior far exceeding those of commercial acrylic and styrenic triblock copolymers.

  7. Facile template-free hydrothermal synthesis and microstrain ...

    Indian Academy of Sciences (India)

    Administrator

    2009), solar cells (Yuan et al 2011), transparent elec- trodes (Kim et al ... increasing the peak width, intensity and shifting the 2θ peak position. ... Facile template-free hydrothermal synthesis and microstrain measurement of ZnO nanorods. 399.

  8. Synthesis of Diopside by Solution Combustion Process Using Glycine Fuel

    Science.gov (United States)

    Sherikar, Baburao N.; Umarji, A. M.

    Nano ceramic Diopside (CaMgSi2O6) powders are synthesized by Solution Combustion Process(SCS) using Calcium nitrate, Magnesium nitrate as oxidizer and glycine as fuel, fumed silica as silica source. Ammonium nitrate (AN) is used as extra oxidizer. Effect of AN on Diopside phase formation is investigated. The adiabatic flame temperatures are calculated theoretically for varying amount of AN according to thermodynamic concept and correlated with the observed flame temperatures. A “Multi channel thermocouple setup connected to computer interfaced Keithley multi voltmeter 2700” is used to monitor the thermal events during the process. An interpretation based on maximum combustion temperature and the amount of gases produced during reaction for various AN compositions has been proposed for the nature of combustion and its correlation with the characteristics of as synthesized powder. These powders are characterized by XRD, SEM showing that the powders are composed of polycrystalline oxides with crystallite size of 58nm to 74nm.

  9. Influence of fuel ratios on auto combustion synthesis of barium ferrite ...

    Indian Academy of Sciences (India)

    Unknown

    Influence of fuel ratios on auto combustion synthesis of barium ferrite nano particles. D BAHADUR*, S RAJAKUMAR and ANKIT KUMAR. Department of Metallurgical Engineering and Materials Science, Indian Institute of Technology,. Mumbai 400 076 e-mail: dhirenb@iitb.ac.in. Abstract. Single-domain barium ferrite nano ...

  10. DEXTROSE-TEMPLATED MICROWAVE-ASSISTED COMBUSTION SYNTHESIS OF SPONGY METAL OXIDES

    Science.gov (United States)

    Microwave-assisted combustion synthesis of porous nanocrystalline titania and carbon coated titania is reported using dextrose as template and the product was compared with the one obtained using conventional heating furnace. Out of three compositions viz., 1:1, 1:3, and 1:5 (met...

  11. Combustion synthesis of TiC-based materials: Mechanisms, densification, and properties

    International Nuclear Information System (INIS)

    LaSalvia, J.C.; Meyers, M.A.

    1995-01-01

    The micromechanisms involved in the combustion synthesis of a Ti-C-Ni-Mo mixture resulting in the formation of a TiC-based composite were examined using the combustion wave quenching technique developed by Rogachev et al. At the micron level, the main reaction occurs at the interface between a Ti-Ni-C melt and C particles, resulting in the formation of a solid TiC x layer on the C particles. This layer undergoes a successive process of rapid growth and decomposition into TiC x spherules until all of the C particle is consumed. This mechanism is consistent with the apparent activation energy (E = 100 kJ/mol) for the process obtained from a macrokinetic investigation of the system. The apparent uniformity in size (d = 1 μm) of the TiC x spherules upon formation indicates a critical condition in the stability of the energetics involved in the process. These TiC x spherules undergo growth due to Ostwald ripening and coalescence mechanisms resulting in a final apparent size of 2.5 μm. For the compositions investigated, the addition of Mo did not affect either the micromechanisms or macrokinetics of the combustion synthesis process. Densification of the porous body after the combustion synthesis process can be carried out while it is still in a easily deformable state. The highly porous body is densified by a combination of fracture (communition), plastic deformation, and sintering. The mechanisms are identified for the case of combustion synthesized TiC. Mechanical properties and microstructures of a number of materials (e.g. TiC, TiB 2 , Al 2 O 3 -TiB 2 , TiB 2 -SiC, TiC-Ni-Mo) produced by combustion synthesis combined with a high-velocity forging step are reviewed

  12. The use of an electric field as a processing parameter in the combustion synthesis of ceramics and composites

    International Nuclear Information System (INIS)

    Munir, Z.A.

    1996-01-01

    The imposition of an electric field is shown to activate self-propagating combustion reactions and thus makes possible the synthesis of a variety of ceramic and composite phases. Experimental observations and modeling studies indicated that activation is accomplished by the localized effect of the current. The relationship between wave propagation and the direction of the applied field was investigated. The synthesis of composites by field-activated combustion synthesis (FACS) was demonstrated. It was shown that the imposition of a field during the combustion synthesis of MoSi 2 results in a decrease /in the product particle size. The results suggest that the field can be used as a processing parameter in self-propagating combustion synthesis

  13. Synthesis and characterization of actinide metal compounds formed by combustion

    International Nuclear Information System (INIS)

    Behrens, R.G.; King, M.A.

    1985-01-01

    This paper briefly describes the results of attempts to synthesize arsenides, phosphides, and antimonides of uranium and thorium using Self-Propagating High-Temperature Synthesis (SHS) techniques. This paper first summarizes the chemistry and thermodynamics of these chemical systems, describes SHS synthesis techniques, and then describes the results of the syntheses using data from powder x-ray diffraction, metallographic, and electron microprobe analyses

  14. Design and Testing of a Breadboard Electrical Power Control Unit for the Fluid Combustion Facility Experiment

    Science.gov (United States)

    Kimnach, Greg L.; Lebron, Ramon C.

    1999-01-01

    The Fluid Combustion Facility (FCF) Project and the Power Technology Division at the NASA Glenn Research Center (GRC) at Lewis Field in Cleveland, OH along with the Sundstrand Corporation in Rockford, IL are jointly developing an Electrical Power Converter Unit (EPCU) for the Fluid Combustion Facility to be flown on the International Space Station (ISS). The FCF facility experiment contains three racks: A core rack, a combustion rack, and a fluids rack. The EPCU will be used as the power interface to the ISS 120V(sub dc) power distribution system by each FCF experiment rack which requires 28V(sub dc). The EPCU is a modular design which contains three 120V(sub dc)-to-28V(sub dc) full-bridge, power converters rated at 1 kW(sub e) each bus transferring input relays and solid-state, current-limiting input switches, 48 current-limiting, solid-state, output switches; and control and telemetry hardware. The EPCU has all controls required to autonomously share load demand between the power feeds and--if absolutely necessary--shed loads. The EPCU, which maximizes the usage of allocated ISS power and minimizes loss of power to loads, can be paralleled with other EPCUs. This paper overviews the electrical design and operating characteristics of the EPCU and presents test data from the breadboard design.

  15. Solution combustion synthesis of metal oxide nanomaterials for energy storage and conversion

    Science.gov (United States)

    Li, Fa-Tang; Ran, Jingrun; Jaroniec, Mietek; Qiao, Shi Zhang

    2015-10-01

    The design and synthesis of metal oxide nanomaterials is one of the key steps for achieving highly efficient energy conversion and storage on an industrial scale. Solution combustion synthesis (SCS) is a time- and energy-saving method as compared with other routes, especially for the preparation of complex oxides which can be easily adapted for scale-up applications. This review summarizes the synthesis of various metal oxide nanomaterials and their applications for energy conversion and storage, including lithium-ion batteries, supercapacitors, hydrogen and methane production, fuel cells and solar cells. In particular, some novel concepts such as reverse support combustion, self-combustion of ionic liquids, and creation of oxygen vacancies are presented. SCS has some unique advantages such as its capability for in situ doping of oxides and construction of heterojunctions. The well-developed porosity and large specific surface area caused by gas evolution during the combustion process endow the resulting materials with exceptional properties. The relationship between the structural properties of the metal oxides studied and their performance is discussed. Finally, the conclusions and perspectives are briefly presented.

  16. Mixture of fuels for solution combustion synthesis of porous Fe3O4 powders

    Science.gov (United States)

    Parnianfar, H.; Masoudpanah, S. M.; Alamolhoda, S.; Fathi, H.

    2017-06-01

    The solution combustion synthesis of porous magnetite (Fe3O4) powders by a mixture of glycine and urea fuels was investigated concerning the thermodynamic aspects and powder characteristics. The adiabatic combustion temperature and combusted species were thermodynamically calculated as a function of the fuel to oxidant molar ratio (ϕ). The combustion behavior, phase evolution, porous structure and magnetic properties were characterized by thermal analysis, X-ray diffractometry, N2 adsorption-desorption, electron microscopy and vibrating sample magnetometry techniques. Nearly single phase Fe3O4 powders were synthesized by the mixture of fuels at ϕ values of 0.75 and 1. The as-combusted Fe3O4 powders at ϕ = 1 exhibited porous structure with the specific surface area of 83.4 m2/g. The highest saturation magnetization of 75.5 emu/g and the lowest coercivity of 84 Oe were achieved at ϕ = 1, due to the high purity and large crystallite size, inducing from the highest adiabatic combustion temperature.

  17. Results concerning a clean co-combustion technology of waste biomass with fossil fuel, in a pilot fluidised bed combustion facility

    Energy Technology Data Exchange (ETDEWEB)

    Ionel, Ioana; Trif-Tordai, Gavril; Ungureanu, Corneliu; Popescu, Francisc; Lontis, Nicolae [Politehnica Univ. Timisoara (Romania). Faculty for Mechanical Engineering

    2008-07-01

    The research focuses on a facility, the experimental results, interpretation and future plans concerning a new developed technology of using waste renewable energy by applying the cocombustion of waste biomass with coal, in a fluidised bed system. The experimental facility is working entirely in accordance to the allowed limits for the exhaust flue gas concentration, with special concern for typical pollutants. The experiments conclude that the technology is cleaner, has as main advantage the possibility to reduce both the SO{sub 2} and CO{sub 2} exhaust in comparison to standard fossil fuel combustion, under comparable circumstances. The combustion is occurring in a stable fluidised bed. (orig.)

  18. Effects of boron addition on the formation of MoSi2 by combustion synthesis mode

    International Nuclear Information System (INIS)

    Feng Peizhong; Wu Jie; Islam, S.H.; Liu Weisheng; Niu Jinan; Wang Xiaohong; Qiang Yinghuai

    2010-01-01

    The combustion synthesis behavior of Mo-Si-B powder was investigated. Test specimens with nominal compositions including MoSi 2 , Mo(Si 0.975 B 0.025 ) 2 , Mo(Si 0.95 B 0.05 ) 2 , Mo(Si 0.925 B 0.075 ) 2 and Mo(Si 0.9 B 0.1 ) 2 were employed. The combustion mode, propagation velocity of combustion wave, combustion temperature and combustion product structure were studied. The results showed that the combustion wave propagated along a spiral trajectory till reaching the bottom of the compacts. The combustion temperature was increased by the addition of boron, to as high as 1922 K in the case of the Mo(Si 0.95 B 0.05 ) 2 sample. However, the flame-front propagation velocity decreased as a result of the addition of boron. The X-ray diffraction results showed that the combustion products of the Mo(Si 0.975 B 0.025 ) 2 and Mo(Si 0.9 B 0.1 ) 2 samples were composed of MoSi 2 with minor MoB. Those of the Mo(Si 0.95 B 0.05 ) 2 and Mo(Si 0.925 B 0.075 ) 2 samples were composed of MoSi 2 with minor MoB and MoB 2 . And traces of Mo 2 B 5 were identified in the Mo(Si 0.95 B 0.05 ) 2 sample.

  19. Facile and Green Synthesis of Saturated Cyclic Amines

    Directory of Open Access Journals (Sweden)

    Arruje Hameed

    2017-10-01

    Full Text Available Single-nitrogen containing saturated cyclic amines are an important part of both natural and synthetic bioactive compounds. A number of methodologies have been developed for the synthesis of aziridines, azetidines, pyrrolidines, piperidines, azepanes and azocanes. This review highlights some facile and green synthetic routes for the synthesis of unsubstituted, multisubstituted and highly functionalized saturated cyclic amines including one-pot, microwave assisted, metal-free, solvent-free and in aqueous media.

  20. Hydrogen detonation and detonation transition data from the High-Temperature Combustion Facility

    International Nuclear Information System (INIS)

    Ciccarelli, G.; Boccio, J.L.; Ginsberg, T.; Finfrock, C.; Gerlach, L.; Malliakos, A.

    1995-01-01

    The BNL High-Temperature Combustion Facility (HTCF) is an experimental research tool capable of investigating the effects of initial thermodynamic state on the high-speed combustion characteristic of reactive gas mixtures. The overall experimental program has been designed to provide data to help characterize the influence of elevated gas-mixture temperature (and pressure) on the inherent sensitivity of hydrogen-air-steam mixtures to undergo detonation, on the potential for flames accelerating in these mixtures to transition into detonations, on the effects of gas venting on the flame-accelerating process, on the phenomena of initiation of detonations in these mixtures by jets of hot reactant product,s and on the capability of detonations within a confined space to transmit into another, larger confined space. This paper presents results obtained from the completion of two of the overall test series that was designed to characterize high-speed combustion phenomena in initially high-temperature gas mixtures. These two test series are the intrinsic detonability test series and the deflagration-to-detonation (DDT) test series. A brief description of the facility is provided below

  1. Hydrogen detonation and detonation transition data from the High-Temperature Combustion Facility

    International Nuclear Information System (INIS)

    Ciccarelli, G.; Boccio, J.L.; Ginsberg, T.; Finfrock, C.

    1996-01-01

    The BNL High-Temperature Combustion Facility (HTCF) is an experimental research tool capable of investigating the effects of initial thermodynamic state on the high-speed combustion characteristic of reactive gas mixtures. The overall experimental program has been designed to provide data to help characterize the influence of elevated gas-mixture temperature (and pressure) on the inherent sensitivity of hydrogen-air-steam mixtures to undergo detonation, on the potential for flames accelerating in these mixtures to transition into detonations, on the effects of gas venting on the flame-accelerating process, on the phenomena of initiation of detonations in these mixtures by jets of hot reactant products, and on the capability of detonations within a confined space to transmit into another, larger confined space. This paper presents results obtained from the completion of two of the overall test series that was designed to characterize high-speed combustion phenomena in initially high-temperature gas mixtures. These two test series are the intrinsic detonability test series and the deflagration-to-detonation (DDT) test series. A brief description of the facility is provided below

  2. Visible and NIR luminescence of nanocrystalline β-Ga2O3:Er3+ prepared by solution combustion synthesis

    International Nuclear Information System (INIS)

    Biljan, Tomislav; Gajovic, Andreja; Meic, Zlatko

    2008-01-01

    In this paper we report on facile solution combustion synthesis of erbium doped β-Ga 2 O 3 with urea as fuel. The product was characterized using powder X-ray diffraction and transmission electron microscopy (TEM). X-ray diffraction and TEM showed that the material is nanostructured. Luminescence properties of β-Ga 2 O 3 :Er are studied with excitation in near infrared (Nd:YAG laser at 1064 nm) and visible (argon laser at 514.5 nm). A strong NIR emission of Er 3+ in the window of minimal optical loss in silica based optical fibers, due to the 4 I 13/2 → 4 I 15/2 transition at 1.55 μm has been observed. Codoping with Yb 3+ significantly increases the intensity of that important emission

  3. Facile Synthesis of N -Substituted Benzimidazoles

    NARCIS (Netherlands)

    Kurhade, Santosh; Rossetti, Arianna; Dömling, Alexander

    2016-01-01

    A particularly mild and efficient one-pot synthesis of N-substituted benzimidazole derivatives was developed. 2-Fluoro-5-nitrophenylisocyanide reacts with a diverse set of primary amines to afford the respective products in moderate to very good yield (35-95%; 20 examples).

  4. Synthesis of nano-sized hydroxyapatite powders through solution combustion route under different reaction conditions

    International Nuclear Information System (INIS)

    Ghosh, Samir Kumar; Roy, Sujit Kumar; Kundu, Biswanath; Datta, Someswar; Basu, Debabrata

    2011-01-01

    Calcium hydroxyapatite, Ca 10 (PO 4 ) 6 (OH) 2 (HAp) was synthesized by combustion in the aqueous system containing calcium nitrate-diammonium hydrogen orthophosphate with urea and glycine as fuels. These ceramics are important materials for biomedical applications. Thermo-gravimetric and differential thermal analysis were employed to understand the nature of synthesis process during combustion. Effects of different process parameters namely, nature of fuel (urea and glycine), fuel to oxidizer ratio (0.6-4.0) and initial furnace temperature (300-700 o C) on the combustion behavior as well as physical properties of as-formed powders were investigated. A series of combustion reactions were carried out to optimize the reaction parameters for synthesis of nano-sized HAp powders. The combustion temperature (T f ) for the oxidant and fuels were calculated to be 896 deg. C and 1035 deg. C for the stoichiometric system of urea and glycine respectively. The stoichiometric glycine-calcium nitrate produced higher flame temperature (both calculated and measured) and powder with lower specific surface area (8.75 m 2 /g) compared to the stoichiometric urea-calcium nitrate system (10.50 m 2 /g). Fuel excess combustion in both glycine and urea produced powders with higher surface area. Nanocrystalline HAp powder could be synthesized in situ with a large span of fuel to oxidizer ratio (φ) in case of urea system (0.8 < φ < 4) and (0.6 < φ < 1.5) for the glycine system. Calcium hydroxyapatite particles having diameters ranging between 20 nm and 120 nm could be successfully synthesized through optimized process variable.

  5. A synthesis of carbon dioxide emissions from fossil-fuel combustion

    DEFF Research Database (Denmark)

    Andres, R.J.; Boden, T.A.; Bréon, F.-M.

    2012-01-01

    This synthesis discusses the emissions of carbon dioxide from fossil-fuel combustion and cement production. While much is known about these emissions, there is still much that is unknown about the details surrounding these emissions. This synthesis explores our knowledge of these emissions in terms......; and the uncertainties associated with these different aspects of the emissions. The magnitude of emissions from the combustion of fossil fuels has been almost continuously increasing with time since fossil fuels were first used by humans. Despite events in some nations specifically designed to reduce emissions......, or which have had emissions reduction as a byproduct of other events, global total emissions continue their general increase with time. Global total fossilfuel carbon dioxide emissions are known to within 10% uncertainty (95% confidence interval). Uncertainty on individual national total fossil-fuel carbon...

  6. The Effect of Gravity on the Combustion Synthesis of Porous Biomaterials

    Science.gov (United States)

    Castillo, M.; Zhang, X.; Moore, J. J.; Schowengerdt, F. D.; Ayers, R. A.

    2003-01-01

    Production of highly porous composite materials by traditional materials processing is limited by difficult processing techniques. This work investigates the use of self propagating high temperature (combustion) synthesis (SHS) to create porous tricalcium phosphate (Ca3(PO4)2), TiB-Ti, and NiTi in low and microgravity. Combustion synthesis provides the ability to use set processing parameters to engineer the required porous structure suitable for bone repair or replacement. The processing parameters include green density, particle size, gasifying agents, composition, and gravity. The advantage of the TiB-Ti system is the high level of porosity achieved together with a modulus that can be controlled by both composition (TiB-Ti) and porosity. At the same time, NiTi exhibits shape memory properties. SHS of biomaterials allows the engineering of required porosity coupled with resorbtion properties and specific mechanical properties into the composite materials to allow for a better biomaterial.

  7. The large-scale vented combustion test facility at AECL-WL: description and preliminary test results

    International Nuclear Information System (INIS)

    Loesel Sitar, J.; Koroll, G.W.; Dewit, W.A.; Bowles, E.M.; Harding, J.; Sabanski, C.L.; Kumar, R.K.

    1997-01-01

    Implementation of hydrogen mitigation systems in nuclear reactor containments requires testing the effectiveness of the mitigation system, reliability and availability of the hardware, potential consequences of its use and the technical basis for hardware placement, on a meaningful scale. Similarly, the development and validation of containment codes used in nuclear reactor safety analysis require detailed combustion data from medium- and large-scale facilities. A Large-Scale Combustion Test Facility measuring 10 m x 4 m x 3 m (volume, 120 m 3 ) has been constructed and commissioned at Whiteshell Laboratories to perform a wide variety of combustion experiments. The facility is designed to be versatile so that many geometrical configurations can be achieved. The facility incorporates extensive capabilities for instrumentation and high speed data acquisition, on-line gas sampling and analysis. Other features of the facility include operation at elevated temperatures up to 150 degrees C, easy access to the interior, and remote operation. Initial thermodynamic conditions in the facility can be controlled to within 0.1 vol% of constituent gases. The first series of experiments examined vented combustion in the full 120 m 3 -volume configuration with vent areas in the range of 0.56 to 2.24 m 2 . The experiments were performed at ∼27 degrees C and near-atmospheric pressures, with hydrogen concentrations in the range of 8 to 12% by volume. This paper describes the Large-Scale Vented Combustion Test Facility and preliminary results from the first series of experiments. (author)

  8. Formation Mechanism of Spherical TiC in Ni-Ti-C System during Combustion Synthesis.

    Science.gov (United States)

    Zhu, Guoliang; Wang, Wei; Wang, Rui; Zhao, Chuanbao; Pan, Weitao; Huang, Haijun; Du, Dafan; Wang, Donghong; Shu, Da; Dong, Anping; Sun, Baode; Jiang, Sheng; Pu, Yilong

    2017-08-29

    The formation mechanism of TiC particles in a Ni-Ti-C system were revealed by using differential thermal analysis (DTA), XRD, and SEM to identify the reaction products in different temperature ranges. The results indicated that the synthesis mechanism of TiC in Ni-Ti-C system was complex; several reactions were involved in the combustion synthesis of TiC-Ni composite. The Ni-Ti intermediate phases play important roles during the formation of TiC. Moreover, the influence of heating rate on the size range of TiC was also discussed.

  9. Facile Synthesis of Permethyl Yttrocene Hydride

    NARCIS (Netherlands)

    Haan, Klaas H. den; Teuben, Jan H.

    1984-01-01

    A convenient three step synthesis of (Cp*2YH)n (Cp* = C5Me5) is described starting with YCl3.3thf, in which Cp*2YCl.thf and Cp*2YCH(SiMe3)2 are intermediates, which could be isolated and characterized. The hydride is active in the activation of sp2 and sp3 C-H bonds as was demonstrated by the H-D

  10. Synthesis of Li2MO3 (M = Ti or Zr) by the combustion method

    International Nuclear Information System (INIS)

    Cruza, D.; Bulbuliana, S.; Cruza, D.; Pfeifferc, H.

    2006-01-01

    The advantages and disadvantages of the combustion method to prepare Li 2 TiO 3 and Li 2 ZrO 3 ceramics were studied. Firstly, the ceramic powders were prepared by the combustion process using LiOH, MO 2 (where M=Ti or Zr) and urea in different molar ratios (from 2:1:3 to 3:1:3) at different temperatures for 5 minutes. Li 2 TiO 3 and Li 2 ZrO 3 were also obtained by the solid-state method, and the results were compared with those obtained by the combustion process. The powders were characterized by X-ray diffraction and scanning electron microscopy. It was found that the combustion process reduces the synthesis time of Li 2 TiO 3 (1 minute at 750 C), but it does not have any advantage on producing Li 2 ZrO 3 , due to thermodynamic factors. On the other hand, the combustion process produces carbon contaminants in the solids. It was necessary to add excess of lithium hydroxide, in order to compensate the quantity of Li sublimated during the production of the ceramics. Finally, it seems that both reactions follow the same mechanism, which is determined by the lithium diffusion into the metal oxides. (authors)

  11. Fabrication of a Spherical Titanium Powder by Combined Combustion Synthesis and DC Plasma Treatment

    Directory of Open Access Journals (Sweden)

    Choi S.H.

    2017-06-01

    Full Text Available Combustion synthesis is capable of producing many types of refractory and ceramic materials, as well as metals, with a relatively lower cost and shorter time frame than other solid state synthetic techniques. TiO2 with Mg as reductant were dry mixed and hand compacted into a 60 mm diameter mold and then combusted under an Ar atmosphere. Depending on the reaction parameters (Mg concentration 2 ≤ α ≤ 4, the thermocouples registered temperatures between 1160°C and 1710°C · 3 mol of Mg gave the optimum results with combustion temperature (Tc and combustion velocity (Uc values of 1372°C and 0.26 cm/s respectively. Furthermore, this ratio also had the lowest oxygen concentration in this study (0.8 wt%. After combustion, DC plasma treatment was carried out to spheroidize the Ti powder for use in 3D printing. The characterization of the final product was performed using X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, and N/O analysis.

  12. Effect of the container in the synthesis of the combustion reaction of ZnAl2O4

    International Nuclear Information System (INIS)

    Silva, D.A.R.; Cavalcanti, L.R.C.; Moura, A.L.S.; Rocha, M.L.; Neto, O.L.A.; Cabral, I.C.; Viana, K.M.S.; Costa, A.C.F.M.

    2012-01-01

    In the present work is a study on the influence of the container in the synthesis of the combustion reaction ZnAl 2 O 4 . Products of combustion obtained for both synthesis routes, were broken and sieved in 325 mesh (44μm). The powders resulting from two types of synthesis were characterized by X-ray diffraction and scanning electron microscopy. By means of XRD analysis showed the formation of the main phase of zinc aluminate spinel (Z) as phase the mineral guanine in the two procedures synthesis. By means of SEM analysis showed that in the procedure used the crucible metal zinc aluminate is introduced in the form of smaller agglomerates. Therefore, the container used in the synthesis of combustion influences the microstructure of the material synthesized. (author)

  13. High-gravity combustion synthesis and in situ melt infiltration: A new method for preparing cemented carbides

    International Nuclear Information System (INIS)

    Liu, Guanghua; Li, Jiangtao; Yang, Zengchao; Guo, Shibin; Chen, Yixiang

    2013-01-01

    A new method of high-gravity combustion synthesis and in situ melt infiltration is reported for preparing cemented carbides, where hot nickel melt is in situ synthesized from a highly exothermic combustion reaction and then infiltrated into tungsten carbide powder compacts. The as-prepared sample showed a homogeneous microstructure, and its relative density, hardness and flexural strength were 94.4%, 84 HRA and 1.49 GPa, respectively. Compared with conventional powder metallurgy approaches, high-gravity combustion synthesis offers a fast and furnace-free way to produce cemented carbides

  14. Preparation of molybdenum borides by combustion synthesis involving solid-phase displacement reactions

    International Nuclear Information System (INIS)

    Yeh, C.L.; Hsu, W.S.

    2008-01-01

    Preparation of molybdenum borides of five different phases in the Mo-B binary system (including Mo 2 B, MoB, MoB 2 , Mo 2 B 5 , and MoB 4 ) was performed by self-propagating high-temperature synthesis (SHS) with two kinds of the reactant samples. When elemental powder compacts with an exact stoichiometry corresponding to the boride phase were employed, self-sustaining reaction was only achieved in the sample with Mo:B = 1:1 and nearly single-phase MoB was yielded. Therefore, the other four boride compounds were prepared from the reactant compacts composed of MoO 3 , Mo, and B powders, within which the displacement reaction of MoO 3 with boron was involved in combustion synthesis. Experimental evidence shows that the extent of displacement reaction in the overall reaction has a significant impact on sustainability of the synthesis reaction, combustion temperature, reaction front velocity, and composition of the end product. An increase in the solid-phase displacement reaction taking place during the SHS process contributes more heat flux to the synthesis reaction, thus resulting in the increase of combustion temperature and enhancement of the reaction front velocity. Based upon the XRD analysis, formation of Mo 2 B, MoB 2 , and Mo 2 B 5 as the dominant boride phase in the end product was successful through the SHS reaction with powder compacts under appropriate stoichiometries between MoO 3 , Mo, and B. However, a poor conversion was observed in the synthesis of MoB 4 . The powder compact prepared for the production of MoB 4 yielded mostly Mo 2 B 5

  15. A facile approach for the synthesis of indenoimidazole derivatives ...

    Indian Academy of Sciences (India)

    J. Chem. Sci. Vol. 128, No. 12, December 2016, pp. 1841–1847. c Indian Academy of Sciences. DOI 10.1007/s12039-016-1181-2. A facile approach for the synthesis of ... pounds 1 and 2 are presented here in terms of crystal engineering and supramolecular chemistry. ... zoles are heterocyclic organic compounds of wide.

  16. Hot Gas Cleanup Test Facility for gasification and pressurized combustion. Quarterly report, October--December 1994

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-02-01

    The objective of this project is to evaluate hot gas particle control technologies using coal-derived gas streams. This will entail the design, construction, installation, and use of a flexible test facility which can operate under realistic gasification and combustion conditions. The major particulate control device issues to be addressed include the integration of the particulate control devices into coal utilization systems, on-line cleaning techniques, chemical and thermal degradation of components, fatigue or structural failures, blinding, collection efficiency as a function of particle size, and scale-up of particulate control systems to commercial size. The conceptual design of the facility was extended to include a within scope, phased expansion of the existing Hot Gas Cleanup Test Facility Cooperative Agreement to also address systems integration issues of hot particulate removal in advanced coal-based power generation systems. This expansion included the consideration of the following modules at the test facility in addition to the original Transport Reactor gas source and Hot Gas Cleanup Units: carbonizer/pressurized circulating fluidized bed gas source; hot gas cleanup units to mate to all gas streams; combustion gas turbine; and fuel cell and associated gas treatment. The major emphasis during this reporting period was continuing the detailed design of the facility and integrating the particulate control devices (PCDs) into structural and process designs. Substantial progress in underground construction activities was achieved during the quarter. Delivery and construction of coal handling and process structural steel began during the quarter. Delivery and construction of coal handling and process structural steel began during the quarter. MWK equipment at the grade level and the first tier are being set in the structure.

  17. Manufacturing of Porous Al-Cr Preforms for Composite Reinforcing Using Microwave Activated Combustion Synthesis

    Directory of Open Access Journals (Sweden)

    Naplocha K.

    2014-10-01

    Full Text Available The combustion synthesis of porous skeletons (preforms of intermetallic Al–Cr compounds intended for metal matrix composite MMC reinforcing was developed. Mixture of Al and Cr powders with granularity of −10, −44, −74mm were cold isostatic pressed and next ignited and synthetized in a microwave reactor under argon atmosphere (microwave-activated combustion synthesis MACS. In order to ignite the synthesis, microwave energy was focused by a tuner on the specimen. The analysis of reaction temperature diagrams revealed that the synthesis proceeded through the following peritectic transformations: L(liquidus+Al7Cr→L+Al11Cr2→L+Al4Cr. Moreover, EDS and XRD examinations showed that the reaction proceeded between a solid Cr and a liquid Al to create a distinct envelope of Al9Cr4 on Cr particle which next extended and spreaded over the entire structure. The produced preforms with uniform structure and interconnected porosity were infiltrated with liquid Cu and Al alloy. The obtained composite materials exhibited high hardness, wear and distinct temperature oxidation resistance.

  18. Magneto-thermal and dielectric properties of biferroic YCrO3 prepared by combustion synthesis

    International Nuclear Information System (INIS)

    Duran, A.; Arevalo-Lopez, A.M.; Castillo-Martinez, E.; Garcia-Guaderrama, M.; Moran, E.; Cruz, M.P.; Fernandez, F.; Alario-Franco, M.A.

    2010-01-01

    Microstructural, magnetothermal and dielectric properties of YCrO 3 powders prepared by combustion and solid state methods have been studied by a combination of XRD, specific heat, magnetization and permittivity measurements. The TEM and XRD characterization confirm that the combustion powders are amorphous plate-like agglomerates of nano-sized crystalline particles. A more uniform grain size along with an increase of the relative density is observed by SEM in the sintered samples prepared by combustion route with respect to those produced by solid state reaction. Similar to the material obtained through solid state synthesis, the material prepared by the combustion method also shows spin canted antiferromagnetic ordering of Cr +3 (S=3/2) at ∼140 K, which is shown by magnetization as well as λ-type anomaly in the total specific heat. Furthermore, the magnetic contribution to the total specific heat reveals spin fluctuations above T N and a spin reorientation transition at about 60 K. Both YCrO 3 compounds show a diffuse phase transition at about 450 K, typical of a relaxor ferroelectric, which is characterized by a broad peak in the real part of the dielectric permittivity as a function of temperature, with the peak decreasing in magnitude and shifting to higher temperature as the frequency increases. The relaxor dipoles are due to the local non-centrosymmetric structure. Furthermore, the high loss tangent in a broad range of temperature as well as conductivity analysis indicates a hopping mechanism for the electronic conductivity as we believe it is a consequence of the outer d 3 -shell, which have detrimental effects on the polarization and the pooling process in the YCrO 3 bulk material. The more uniform particle size and higher density material synthesized through the combustion process leads to an improvement in the dielectric Properties. - Graphical abstract: Combustion method: An alternative route for synthesized a new family of multiferroics. Amorphous

  19. Direct recovery of boiler residue by combustion synthesis.

    Science.gov (United States)

    Nourbaghaee, Homan; Ghaderi Hamidi, Ahmad; Pourabdoli, Mahdi

    2018-04-01

    Boiler residue (BR) of thermal power plants is one of the important secondary sources for vanadium production. In this research, the aluminothermic self-propagating high-temperature synthesis (SHS) was used for recovering the transition metals of BR for the first time. The effects of extra aluminum as reducing agent and flux to aluminum ratio (CaO/Al) were studied and the efficiency of recovery and presence of impurities were measured. Aluminothermic reduction of vanadium and other metals was carried out successfully by SHS without any foreign heat source. Vanadium, iron, and nickel principally were reduced and gone into metallic master alloy as SHS product. High levels of efficiency (>80%) were achieved and the results showed that SHS has a great potential to be an industrial process for BR recovery. SHS produced two useful products. Metallic master alloy and fused glass slag that is applicable for ceramic industries. SHS can also neutralize the environmental threats of BR by a one step process. Copyright © 2018 Elsevier Ltd. All rights reserved.

  20. Combustion synthesis of CaSc2O4:Ce3+ nano-phosphors in a closed system

    International Nuclear Information System (INIS)

    Peng Wenfang; Zou Shaoyu; Liu Guanxi; Xiao Quanlan; Zhang Rui; Xie Lijuan; Cao Liwei; Meng Jianxin; Liu Yingliang

    2011-01-01

    Highlights: → CaSc 2 O 4 :Ce 3+ nano-phosphors can be prepared by a single-step combustion method. → The ignition temperature is the lowest in the combustion synthesis of Ce 3+ /Eu 2+ doped phosphors. → The as-prepared nano-phosphors give a uniform particle size in the range of 15-20 nm and have highly dispersity and fluorescence intensity. → It is a convenient method for preparation of monodispersed oxide nano-phosphors, especially those being sensitive to air at high temperature. - Abstract: The CaSc 2 O 4 :Ce 3+ nano-phosphors were successfully prepared by a single-step combustion method at an ignition temperature as low as 200 deg. C in a closed autoclave using glycine as a fuel and PEG4000 as a dispersant. The samples were characterized by X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscope (TEM). The results revealed that CaSc 2 O 4 :Ce 3+ nano-phosphors can be conveniently prepared at an ignition temperature as low as 200 deg. C, which was much lower than that in the ordinary combustion methods. The optimized ignition temperature was 220 deg. C. The CaSc 2 O 4 :Ce 3+ nano-phosphors give a uniform particle size in the range of 15-20 nm. The low ignition temperature and the addition of PEG4000 dispersant play important roles in the formation of small sized nanoparticles. The as-prepared nano-phosphors were incompact aggregates, but highly dispersed nano-phosphors can be obtained after further ultrasonic treatment. The CaSc 2 O 4 :Ce 3+ nano-phosphors give satisfactory luminescence characteristic benefiting from the closed circumstance, in which cerium atoms can be isolated from the oxidizing atmosphere and non-fluorescent Ce 4+ ions can be ruled out. The present highly dispersed CaSc 2 O 4 :Ce 3+ nano-phosphors with efficient fluorescence are promising in the field of biological labeling, and the present low temperature combustion method is facile and convenient and can

  1. A synthesis of carbon dioxide emissions from fossil-fuel combustion

    Directory of Open Access Journals (Sweden)

    R. J. Andres

    2012-05-01

    Full Text Available This synthesis discusses the emissions of carbon dioxide from fossil-fuel combustion and cement production. While much is known about these emissions, there is still much that is unknown about the details surrounding these emissions. This synthesis explores our knowledge of these emissions in terms of why there is concern about them; how they are calculated; the major global efforts on inventorying them; their global, regional, and national totals at different spatial and temporal scales; how they are distributed on global grids (i.e., maps; how they are transported in models; and the uncertainties associated with these different aspects of the emissions. The magnitude of emissions from the combustion of fossil fuels has been almost continuously increasing with time since fossil fuels were first used by humans. Despite events in some nations specifically designed to reduce emissions, or which have had emissions reduction as a byproduct of other events, global total emissions continue their general increase with time. Global total fossil-fuel carbon dioxide emissions are known to within 10 % uncertainty (95 % confidence interval. Uncertainty on individual national total fossil-fuel carbon dioxide emissions range from a few percent to more than 50 %. This manuscript concludes that carbon dioxide emissions from fossil-fuel combustion continue to increase with time and that while much is known about the overall characteristics of these emissions, much is still to be learned about the detailed characteristics of these emissions.

  2. Mechanical properties of calcium phosphate cements obtained by solution combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Volkmer, Tiago M.; Barreiro, Oscar; Souza, Vania Caldas; Santos, Luis Alberto dos, E-mail: tiagovolkmer@gmail.com, E-mail: oscarbafer@hotmail.com, E-mail: vania.souza@ufrgs.br, E-mail: luis.santos@ufrgs.br [Universidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS (Brazil). Laboratorio de Biomateriais

    2009-07-01

    Bioceramics based on calcium phosphates, especially hydroxyapatite and tricalcium phosphates (TCP) are the most used biomaterials as bone substitutes. The objective of this work is to evaluate the mechanical properties of α-tricalcium phosphate (α-TCP) synthesized by the solution combustion method. The solution combustion synthesis (SCS) can be considered as faster and simpler as other methods, furthermore it allows the obtainment of high purity α-TCP. In the calcium phosphates (CPC), α-TCP reacts with water forming needle like HA, which restrain the movement of grains, increasing mechanical resistance. In the present paper the influence of particle size on mechanical properties of α-TCP cements were evaluated. The α-TCP powder were characterized by XRD, TEM, BET and laser diffraction to asses particle size while the CPC bodies by SEM, Arquimedes method and compression tests. Increasing the milling time, the particle size decreases, resulting in samples with less porosity and consequently with higher compression resistance. (author)

  3. Chemical synthesis of nanocrystalline magnesium aluminate spinel via nitrate-citrate combustion route

    International Nuclear Information System (INIS)

    Saberi, Ali; Golestani-Fard, Farhad; Sarpoolaky, Hosein; Willert-Porada, Monika; Gerdes, Thorsten; Simon, Reinhard

    2008-01-01

    Nanocrystalline magnesium aluminate spinel (MgAl 2 O 4 ) was synthesized using metal nitrates, citric acid and ammonium solutions. The precursor and the calcined powders at different temperatures were characterized by X-ray diffraction (XRD), simultaneous thermal analysis (STA), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The combustion mechanism was also studied by a quadrupole mass spectrometer (QMS) which coupled to STA. The generated heat through the combustion of the mixture of ammonium nitrate and citrate based complexes decreased the synthesis temperature of MgAl 2 O 4 spinel. The synthesized MgAl 2 O 4 spinel at 900 deg. C has faced shape with crystallite size in the range of 18-24 nm

  4. Combustion synthesis of LaFeO{sub 3} sensing nanomaterial

    Energy Technology Data Exchange (ETDEWEB)

    Zaza, F., E-mail: fabio.zaza@enea.it; Serra, E. [ENEA-Casaccia Research Centre, Via Anguillarese 301, 00123 Rome (Italy); Pallozzi, V.; Pasquali, M. [Department of Basic and Applied Sciences for Engineering, La Sapienza University, Via A. Scarpa 14/16, 00161 Rome (Italy)

    2015-06-23

    Since industrial revolution, human activities drive towards unsustainable global economy due to the overexploitation of natural resources and the unacceptable emissions of pollution and greenhouse gases. In order to address that issue, engineering research has been focusing on gas sensors development for monitoring gas emissions and controlling the combustion process sustainability. Semiconductors metal oxides sensors are attractive technology because they require simple design and fabrication, involving high accessibility, small size and low cost. Perovskite oxides are the most promising sensing materials because sensitivity, selectivity, stability and speed-response can be modulated and optimized by changing the chemical composition. One of the most convenient synthesis process of perovskite is the citrate-nitrate auto-combustion method, in which nitrate is the oxidizing agent and citrate is the fuel and the chelating argent in the same time. Since the sensibility of perovskite oxides depends on the defective crystallographic structure and the nanomorphology, the experimental was designed in order to study the dependence of powder properties on the synthesis conditions, such as the solution acidity and the relative amount of metals, nitrates and citric acid. Crystalline structure was studied in depth for defining the effects of synthesis conditions on size, morphology and crystallographic structure of nanopowders of LaFeO{sub 3}.

  5. Synthesis and sintering of nanocrystalline hydroxyapatite powders by citric acid sol-gel combustion method

    International Nuclear Information System (INIS)

    Han Yingchao; Li Shipu; Wang Xinyu; Chen Xiaoming

    2004-01-01

    The citric acid sol-gel combustion method has been used for the synthesis of nanocrystalline hydroxyapatite (HAP) powder from calcium nitrate, diammonium hydrogen phosphate and citric acid. The phase composition of HAP powder was characterized by X-ray powder diffraction analysis (XRD). The morphology of HAP powder was observed by transmission electron microscope (TEM). The HAP powder has been sintered into microporous ceramic in air at 1200 deg. C with 3 h soaking time. The microstructure and phase composition of the resulting HAP ceramic were characterized by scanning electron microscope (SEM) and XRD, respectively. The physical characterization of open porosity and flexural strength have also been carried out

  6. Combustion of stratified hydrogen-air mixtures in the 10.7 m3 Combustion Test Facility cylinder

    International Nuclear Information System (INIS)

    Whitehouse, D.R.; Greig, D.R.; Koroll, G.W.

    1996-01-01

    This paper presents preliminary results from hydrogen concentration gradient combustion experiments in a 10.7 m 3 cylinder. These gradients, also referred to as stratified mixtures, were formed from dry mixtures of hydrogen and air at atmospheric temperature. Combustion pressures, burn fractions and flame speeds in concentration gradients were compared with combustion of well-mixed gases containing equivalent amounts of hydrogen. The studied variables included the quantity of hydrogen in the vessel, the steepness of the concentration gradient, the igniter location, and the initial concentration of hydrogen at the bottom of the vessel. Gradients of hydrogen and air with average concentrations of hydrogen below the downward propagation limit produced significantly greater combustion pressures when ignited at the top of the vessel than well-mixed gases with the same quantity of hydrogen. This was the result of considerably higher burn fractions in the gradients than in the well-mixed gas tests. Above the downward propagation limit, gradients of hydrogen ignited at the top of the vessel produced nearly the same combustion pressures as under well-mixed conditions; both gradients and well-mixed gases had high burn fractions. Much higher flame speeds were observed in the gradients than the well-mixed gases. Gradients and well-mixed gases containing up to 14% hydrogen ignited at the bottom of the vessel produced nearly the same combustion pressures. Above 14% hydrogen, gradients produced lower combustion pressures than well-mixed gases having the same quantity of hydrogen. This can be attributed to lower burn fractions of fuel from the gradients compared with well-mixed gases with similar quantities of hydrogen. When ignited at the bottom of the vessel, 90% of a gradient's gases remained unburned until several seconds after ignition. The remaining gases were then consumed at a very fast rate. (orig.)

  7. Synthesis and characterization of CaTiO3 powder by combustion synthesis process

    International Nuclear Information System (INIS)

    Jung, C. W.; Shin, H. C.; Park, J. Y.; Lee, H. G.; Kim, H. Y.; Hong, K. W.

    2000-01-01

    Synroc is considered as a one of the most promising candidate for HLW solidification. CaTiO 3 , perovskite, which is a component of Synroc, can immobilize lanthanide and actinides by forming solid solutions. Generally most of the radioactive wastes elements were treated as a nitrate form. Therefore, the combustion process using metal nitrates as reactant materials can be easily applied to immobilize the radioactive waste elements. In this study, the feasibility of preparing fine, single-phase powders of multi-component oxide by a combustion process was investigated. Generally, the powder synthesized by combustion process showed different characteristics depending on the type and amount of fuel. And the spherical CaTiO 3 particles were directly prepared from the aqueous solution by an ultrasonic mist combustion process using an ultrasonic nebulizers as mist generators. The particles prepared with simple spray pyrolysis method using nitrate solution without fuel as precursor solution showed porous and hollow morphology, while the particles prepared with precursor solutions containing fuel showed dense solid morphology. Among various kinds of fuel tested, glycine showed the best result in reaction kinetics and crystalline phase purity

  8. Photoluminescence and cathodoluminescence properties of Y2O3:Eu nanophosphors prepared by combustion synthesis

    International Nuclear Information System (INIS)

    Vu, Nguyen; Kim Anh, Tran; Yi, Gyu-Chul; Strek, W.

    2007-01-01

    Eu-doped Y 2 O 3 nanophosphors were prepared using combustion synthesis. In this method, urea was employed as a fuel. The particle size was estimated to be in the range of 10-20 nm as determined by X-ray diffractometry and transmission electron microscopy. The photoluminescent and cathodoluminescent spectra are described by the well-known 5 D 0 →7 F J transition (J=0, 1, 2, etc.) of Eu 3+ ions with the strongest emission for J=2. The optical properties of nanophosphors were compared with commercial with an order of micrometer size. The effects of urea-to-metal nitrate molar ratio and the other synthesis conditions on the particle size and luminescent properties will be discussed in detail. The red emission of Eu-doped Y 2 O 3 nanophosphors is promising materials not only in high-resolution screen but also in telecomunication as well as in biosensor

  9. Evaluation of biological activities of nanocrystalline zirconia synthesis via combustion method

    International Nuclear Information System (INIS)

    Thakare, V.G.; Omanwar, S.K.; Bhatkar, V.B.; Wadegaokar, P.A.

    2016-01-01

    The objective of the following study was synthesis of nanocrystalline zirconia by modified solution combustion synthesis method and evaluation of its structural and biological properties. The sample was characterized by powder X-ray diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM) and evaluated for cytotoxicity study using 3T3 mouse fibroblast cells, the antibacterial property are investigated by spread plate method against E. coli bacterial pathogen and studied for degradation using phosphate buffered saline (PBS) solution. The XRD pattern shows that the monoclinic phase of nanocrystalline zirconia was obtained. The FESEM images showed that the prepared sample consists of particles in the range of 45 nm and homogenous particle size distribution. The sample of zirconia has excellent tissue biocompatibility and does not show any toxicity towards normal 3T3 mouse fibroblast cells. It also inhibited the bacterial growth. The sample shows stability at physiological condition and does not show degradation. (author)

  10. Spatially Resolved Temperature and Water Vapor Concentration Distributions in Supersonic Combustion Facilities by TDLAT

    Science.gov (United States)

    Busa, K. M.; McDaniel J. C.; Diskin, G. S.; DePiro, M. J.; Capriotti, D. P.; Gaffney, R. L.

    2012-01-01

    Detailed knowledge of the internal structure of high-enthalpy flows can provide valuable insight to the performance of scramjet combustors. Tunable Diode Laser Absorption Spectroscopy (TDLAS) is often employed to measure temperature and species concentration. However, TDLAS is a path-integrated line-of-sight (LOS) measurement, and thus does not produce spatially resolved distributions. Tunable Diode Laser Absorption Tomography (TDLAT) is a non-intrusive measurement technique for determining two-dimensional spatially resolved distributions of temperature and species concentration in high enthalpy flows. TDLAT combines TDLAS with tomographic image reconstruction. More than 2500 separate line-of-sight TDLAS measurements are analyzed in order to produce highly resolved temperature and species concentration distributions. Measurements have been collected at the University of Virginia's Supersonic Combustion Facility (UVaSCF) as well as at the NASA Langley Direct-Connect Supersonic Combustion Test Facility (DCSCTF). Due to the UVaSCF s unique electrical heating and ability for vitiate addition, measurements collected at the UVaSCF are presented as a calibration of the technique. Measurements collected at the DCSCTF required significant modifications to system hardware and software designs due to its larger measurement area and shorter test duration. Tomographic temperature and water vapor concentration distributions are presented from experimentation on the UVaSCF operating at a high temperature non-reacting case for water vitiation level of 12%. Initial LOS measurements from the NASA Langley DCSCTF operating at an equivalence ratio of 0.5 are also presented. Results show the capability of TDLAT to adapt to several experimental setups and test parameters.

  11. A novel solution combustion synthesis of cobalt oxide nanoparticles as negative-electrode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    Wen Wei; Wu Jinming; Tu Jiangping

    2012-01-01

    Highlights: ► We examine the electrochemical performance of cobalt oxides fabricated by solution combustion synthesis for rechargeable lithium-ion battery applications. ► The additive of NaF in precursor results in an eruption combustion mode. ► The eruption combustion leads to fluffy networks with smaller grains and more macroporous voids. ► The network contributes to higher discharge capacity, higher initial coulombic efficiency, and better cycling performance for rechargeable lithium-ion batteries. - Abstract: Low cost mass production of cobalt oxide nanoparticles with high electrochemical performance is of practical interest for rechargeable lithium-ion batteries. In this report, cobalt oxide nanoparticles were fabricated by solution combustion synthesis, with the introduction of NaF into the precursor to alter the combustion mode. The novel eruption combustion resulted in fluffy networks with smaller particles and more macroporous voids, which contributed to the higher discharge capacity, higher initial coulombic efficiency, and better cycling performance when compared with that achieved by the conventional combustion mode.

  12. Carbohydrate-Assisted Combustion Synthesis To Realize High-Performance Oxide Transistors.

    Science.gov (United States)

    Wang, Binghao; Zeng, Li; Huang, Wei; Melkonyan, Ferdinand S; Sheets, William C; Chi, Lifeng; Bedzyk, Michael J; Marks, Tobin J; Facchetti, Antonio

    2016-06-08

    Owing to high carrier mobilities, good environmental/thermal stability, excellent optical transparency, and compatibility with solution processing, thin-film transistors (TFTs) based on amorphous metal oxide semiconductors (AOSs) are promising alternatives to those based on amorphous silicon (a-Si:H) and low-temperature (IGZO) TFTs suffer from low carrier mobilities and/or inferior bias-stress stability versus their sputtered counterparts. Here we report that three types of environmentally benign carbohydrates (sorbitol, sucrose, and glucose) serve as especially efficient fuels for IGZO film combustion synthesis to yield high-performance TFTs. The results indicate that these carbohydrates assist the combustion process by lowering the ignition threshold temperature and, for optimal stoichiometries, enhancing the reaction enthalpy. IGZO TFT mobilities are increased to >8 cm(2) V(-1) s(-1) on SiO2/Si gate dielectrics with significantly improved bias-stress stability. The first correlations between precursor combustion enthalpy and a-MO densification/charge transport are established.

  13. Combustion of Na2B4O7 + Mg + C to synthesis B4C powders

    International Nuclear Information System (INIS)

    Jiang Guojian; Xu Jiayue; Zhuang Hanrui; Li Wenlan

    2009-01-01

    Boron carbide powder was fabricated by combustion synthesis (CS) method directly from mixed powders of borax (Na 2 B 4 O 7 ), magnesium (Mg) and carbon. The adiabatic temperature of the combustion reaction of Na 2 B 4 O 7 + 6 Mg + C was calculated. The control of the reactions was achieved by selecting reactant composition, relative density of powder compact and gas pressure in CS reactor. The effects of these different influential factors on the composition and morphologies of combustion products were investigated. The results show that, it is advantageous for more Mg/Na 2 B 4 O 7 than stoichiometric ratio in Na 2 B 4 O 7 + Mg + C system and high atmosphere pressure in the CS reactor to increase the conversion degree of reactants to end product. The final product with the minimal impurities' content could be fabricated at appropriate relative density of powder compact. At last, boron carbide without impurities could be obtained after the acid enrichment and distilled water washing.

  14. A study of Cu/ZnO/Al2O3 methanol catalysts prepared by flame combustion synthesis

    DEFF Research Database (Denmark)

    Jensen, Joakim Reimer; Johannessen, Tue; Wedel, Stig

    2003-01-01

    The flame combustion synthesis of Cu/ZnO/Al2O3 catalysts for the synthesis of methanol from CO, CO2 and H2 is investigated. The oxides are generated in a premixed flame from the acetyl-acetonate vapours of Cu, Zn and Al mixed with the fuel and air prior to combustion. The flame-generated powder...... temperature and quench-cooling of the flame tend to increase the dispersion of the phases and the specific surface area of the particles. Properties of both the ternary composition, the three binary compositions and the pure oxides are discussed. The calculation of simultaneous phase and chemical equilibrium...

  15. Ultrasound assisted combustion synthesis of TiC in Al-Ti-C system.

    Science.gov (United States)

    Liu, Zhiwei; Rakita, Milan; Xu, Wilson; Wang, Xiaoming; Han, Qingyou

    2015-11-01

    This research investigated the effects of high-intensity ultrasound on the combustion synthesis of TiC particles in Al-Ti-C system. The process involved that high-intensity ultrasound was applied on the surface of a compacted Al-Ti-C pellet directly through a Nb probe during the thermal explosion reaction. By comparing with the sample without ultrasonic treatment, it was found that the thermal explosion reaction for synthesizing TiC phase could take place thoroughly in the ultrasonically treated sample. During the process of synthesizing TiC phase, the dissolution of solid graphite particles into the Al-Ti melt, as well as the nucleation and growth of TiC particles could be promoted effectively due to the effects of ultrasound, leading to an enhancement of the formation of TiC particles. Ultrasound assisted combustion synthesis as a simple and effective approach was proposed for synthesizing materials in this research. Copyright © 2015 Elsevier B.V. All rights reserved.

  16. Joining of Ni-TiC FGM and Ni-Al Intermetallics by Centrifugal Combustion Synthesis

    International Nuclear Information System (INIS)

    Ohmi, Tatsuya; Matsuura, Kiyotaka; Iguchi, Manabu; Mizuma, Kiminori

    2008-01-01

    A centrifugal combustion synthesis (CCS) process has been investigated to join a Ni-Al intermetallic compound and a Ni-TiC cermet. The cermet, a tubular graphite mold, and a green compact of reactants consisting of Al, Ni and NiO were set in a centrifugal caster. When the combustion synthesis reaction was induced in the centrifugal force field, a synthesized molten Ni-Al alloy flowed into the graphite mold and joined to the cermet. The soundness of the joint interface depended on the volume percentage of TiC phase in the cermet. A lot of defects were formed near the interface between the Ni-TiC cermet and the cast Ni-Al alloy when the volume percentage of TiC was 50% or higher. For this kind of cermet system, using a functionally graded cermet such as Ni-10 vol.%TiC/Ni-25 vol.%TiC/Ni-50 vol.%TiC overcame this difficulty. The four-point bending strength of the joined specimen consisting of the three-layered FGM cermet and cast Ni-29 mol%Al alloy was 1010 MPa which is close to the result for a Ni-29 mol%Al alloy specimen

  17. Spray-combustion synthesis: efficient solution route to high-performance oxide transistors.

    Science.gov (United States)

    Yu, Xinge; Smith, Jeremy; Zhou, Nanjia; Zeng, Li; Guo, Peijun; Xia, Yu; Alvarez, Ana; Aghion, Stefano; Lin, Hui; Yu, Junsheng; Chang, Robert P H; Bedzyk, Michael J; Ferragut, Rafael; Marks, Tobin J; Facchetti, Antonio

    2015-03-17

    Metal-oxide (MO) semiconductors have emerged as enabling materials for next generation thin-film electronics owing to their high carrier mobilities, even in the amorphous state, large-area uniformity, low cost, and optical transparency, which are applicable to flat-panel displays, flexible circuitry, and photovoltaic cells. Impressive progress in solution-processed MO electronics has been achieved using methodologies such as sol gel, deep-UV irradiation, preformed nanostructures, and combustion synthesis. Nevertheless, because of incomplete lattice condensation and film densification, high-quality solution-processed MO films having technologically relevant thicknesses achievable in a single step have yet to be shown. Here, we report a low-temperature, thickness-controlled coating process to create high-performance, solution-processed MO electronics: spray-combustion synthesis (SCS). We also report for the first time, to our knowledge, indium-gallium-zinc-oxide (IGZO) transistors having densification, nanoporosity, electron mobility, trap densities, bias stability, and film transport approaching those of sputtered films and compatible with conventional fabrication (FAB) operations.

  18. Flash combustion synthesis and characterisation of nanosized proton conducting Yttria-doped barium cerate

    Energy Technology Data Exchange (ETDEWEB)

    Jacquin, M.; Jing, Y.; Essoumhi, A.; Taillades, G.; Jones, D.J.; Roziere, J. [Montpellier Univ., Montpellier (France). Lab. des Agregats Moleculaires et Materiaux Inorganiques

    2007-10-15

    The high conversion efficiency of proton ceramic fuel cells renders them a promising technology for electric power conversion. They also function in an intermediate temperature range (400 to 600 degrees C) where the problem of thermal ageing can be avoided. This paper presented a newly developed flash combustion method for the preparation of proton conducting yttrium-doped barium cerate nanopowders. This quick, safe and low cost route takes advantage of the exothermic and self-sustaining redox reaction between high oxygen content metal salts and a suitable fuel that acts as a reducing agent. The parameters that influence the reaction product are the type of fuel, the fuel to oxidizer ratio, and the ignition temperature. Use of suitable fuel in combustion syntheses ensures stability of the chemical composition and high quality of products, and produces non-toxic gases. In this study, the flash combustion synthesis method was used to ignite the mixture at 600 degrees C. The resulting fine powder was characterized by transmission and scanning electron microscopy, and X-ray diffraction. The resulting nano-sized crystallites allow for the preparation of fully densified materials with densities up to 98 per cent. Water uptake was examined in compressed and sintered samples of BaCe{sub 0.9}Y{sub 0.1}O{sub 2.95} (BCY10). Bulk and total conductivities were determined with impedance spectroscopy in the range 300 to 600 degrees C. Densified yttria doped barium cerate materials show a bulk conductivity of 2.3 x 10{sup -2} S/cm and a total conductivity of 1.2 x 10{sup -2} S/cm at 500 degrees C. The temperature dependence was close to that of the bulk. It was concluded that flash combustion is an interesting alternative method for preparing proton conducting oxides for intermediate temperature fuel cells. 28 refs., 1 tab., 10 figs.

  19. Preparation of porous Al2O3-Ti-C perform by combustion synthesis

    Directory of Open Access Journals (Sweden)

    K.Granat

    2009-04-01

    Full Text Available Using combustion synthesis porous ceramic preforms for composite reinforcing were produced. Prepared mixture of alumina Saffilfibres, Ti powder and graphite flakes, after drying were placed in waveguide of microwave reactor. Supplied with constant power of 540Wmagnetron ignited and maintained reaction in flowing stream of CO2 gas. Al2O3 fibres should improve preliminary endurance of perform,whereas Ti powder processed to hard titanium carbides and oxides. During microwave heating ignited plasma additionally improveprocess and partly fused metallic Ti. Recorded temperature curves were similar for various samples. The highest synthesis temperature revealed samples containing 10% of Al2O3 , 10% of Ti and 5% of graphite, all percentages atomic. Microscopic observation showed considerable microstructure inhomogeneity of some samples. Both irregular component ordering and partly processed Ti particles inside preform exclude them for subsequent infiltration. Chemical analyze EDS of Ti based compounds partly confirmed work purpose, evidencing presence of Ti oxides and carbides. Independently of graphite content these compounds formed folded strips around solid or empty volume. Depends on CO2 availability, reaction could be slowed down resulting in more compacted Ti compounds. Created as a result of combustion synthesis Ti compound after infiltration with liquid metal properly bounded with the matrix. It could be assumed that redox reaction proceeded and on surface of Ti compound alumina and Al-Ti compounds were created. The preforms of proper strength and homogeneous structure were infiltrated with AlSi7Mg by squeeze casting method. In relation to typical composite reinforced only with fibres no significant increase of defects quantity was observed. Preliminary examination of mechanical properties confirmed that assumed work purpose is reasonable.

  20. Reactive melt infiltration of copper in Al–Cr preforms produced through combustion synthesis

    International Nuclear Information System (INIS)

    Naplocha, Krzysztof; Granat, Kazimierz; Kaczmar, Jacek

    2014-01-01

    Highlights: • Determination of microstructure and phase transformation during combustion synthesis and reactive infiltration. • Squeeze casting of Cu inducing reactive infiltration of Al–Cr intermetallic porous preform. • Fabrication of unique composite material resisted to high temperature oxidation. - Abstract: Combustion synthesis of Al–Cr preforms used for infiltration and reinforcing of composite materials was developed. Compacts of powdered Al and Cr with stoichiometric ratio Al/Cr equal to 2/1 were synthesized in a microwave reactor furnished with a pyrometer for controlling phase transformations. Due to low enthalpy of the reaction, green compacts were preheated and ignition occurred together with partial melting of Al at the interface with Cr particles. The synthesis proceeded by peritectic transformations L + Al 7 Cr → L + Al 11 Cr 2 → L + Al 4 Cr, reaching maximum temperature of ca. 1000 °C. Porous structures including residual unprocessed Cr particles were soaked to homogenize them and to transform the phases into the stable intermetallic compound Al 9 Cr 4 . Reactive infiltration of the preforms with molten Cu proceeds along with interfacial diffusion of Al that, released from a preform, infiltrates into the matrix changing its composition to Cu 9 Al 4 (Cr). At the same time, the preform is decomposed and converted into a mixture of globular precipitates of Cr 52 Al 35 Cu 13 embedded in the Cu 47 Al 41 Cr 12 phase. The produced composite materials exhibit significant hardness and oxidation resistance at elevated temperatures. The protective layer is composed of oxides Al 2 O 3 and (AlCu) 2 O 3 created at parabolic constant oxidation rate (k p ) equal to 1.9 × 10 −6 g 2 m −4 s −1

  1. Mixture of fuels for solution combustion synthesis of porous Fe{sub 3}O{sub 4} powders

    Energy Technology Data Exchange (ETDEWEB)

    Parnianfar, H.; Masoudpanah, S.M., E-mail: masoodpanah@iust.ac.ir; Alamolhoda, S.; Fathi, H.

    2017-06-15

    Highlights: • Mixture of glycine and urea fuels was applied for solution combustion synthesis of Fe3O4 powders. • The phase and crystallite size of the as-combusted powders depends on the fuel to oxidant ratio (ϕ). • The maximum density (0.033 cm{sup 3}/g) was observed for the as-combusted powders at ϕ = 1. • The highest Ms of 75.5 emu/g and the lowest Hc of 84 Oe were achieved at ϕ = 1. - Abstract: The solution combustion synthesis of porous magnetite (Fe{sub 3}O{sub 4}) powders by a mixture of glycine and urea fuels was investigated concerning the thermodynamic aspects and powder characteristics. The adiabatic combustion temperature and combusted species were thermodynamically calculated as a function of the fuel to oxidant molar ratio (ϕ). The combustion behavior, phase evolution, porous structure and magnetic properties were characterized by thermal analysis, X-ray diffractometry, N{sub 2} adsorption–desorption, electron microscopy and vibrating sample magnetometry techniques. Nearly single phase Fe{sub 3}O{sub 4} powders were synthesized by the mixture of fuels at ϕ values of 0.75 and 1. The as-combusted Fe{sub 3}O{sub 4} powders at ϕ = 1 exhibited porous structure with the specific surface area of 83.4 m{sup 2}/g. The highest saturation magnetization of 75.5 emu/g and the lowest coercivity of 84 Oe were achieved at ϕ = 1, due to the high purity and large crystallite size, inducing from the highest adiabatic combustion temperature.

  2. Fuel effect on solution combustion synthesis of Co(Cr,Al)2O4 pigments

    International Nuclear Information System (INIS)

    Gilabert, J.; Palacios, M.D.; Sanz, V.; Mestre, S.

    2017-01-01

    The fuel effect on the synthesis of a ceramic pigment with a composition CoCr2−2ΨAl2ΨO4 (0≤Ψ≤1) by means of solution combustion synthesis process (SCS) has been studied. Three different fuels were selected to carry out the synthesis (urea, glycine and hexamethylentetramine (HMT)). Highly foamy pigments with very low density were obtained. Fd-3m spinel-type structure was obtained in all the experiments. Nevertheless, crystallinity and crystallite size of the spinels show significant differences with composition and fuel. The use of glycine along with the chromium-richest composition favours ion rearrangement to obtain the most ordered structure. Lattice parameter does not seem to be affected by fuel, although it evolves with Ψ according to Vegard's law. Colouring power in a transparent glaze shows important variations with composition. On the other hand, fuel effect presents a rather low influence since practically the same shades are obtained. However, it exerts certain effect on luminosity (L*). [es

  3. Manganite perovskite nanoparticles for self-controlled magnetic fluidhyperthermia: about the suitability of an aqueous combustion synthesis route

    Czech Academy of Sciences Publication Activity Database

    Epherre, R.; Duguet, E.; Mornet, S.; Pollert, Emil; Louguet, S.; Lecommandoux, S.; Schatz, Ch.; Goglio, G.

    2011-01-01

    Roč. 21, č. 12 (2011), s. 4393-4401 ISSN 0959-9428 Institutional research plan: CEZ:AV0Z10100521 Keywords : manganese perovskite nanoparticles * aqueouc combustion synthesis Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 5.968, year: 2011

  4. Photoelectroactivity of bismuth vanadate prepared by combustion synthesis: effect of different fuels and surfactants

    Energy Technology Data Exchange (ETDEWEB)

    Afonso, Renata; Serafim, Jessica A.; Lucilha, Adriana C.; Dall' Antonia, Luiz H., E-mail: luizh@uel.br [Universidade Estadual de Londrina (UEL), PR (Brazil). Dept. Quimica. Lab. de Eletroquimica e Materiais; Silva, Marcelo R. [Universidade Estadual Paulista Julio de Mesquita Filho (CTI/UNESP), Bauru, SP (Brazil). Colegio Tecnico Industrial; Lepre, Luiz F.; Ando, Romulo A. [Universidade de Sao Paulo (USP), SP (Brazil). Inst. de Quimica. Lab. de Espectroscopia Molecular

    2014-04-15

    The bismuth vanadate (BiVO{sub 4}) is a semiconductor that has attracted much attention due to the photocatalytic efficiency in the visible light region. The objective of this work was to synthesize monoclinic BiVO{sub 4} by solution combustion synthesis, with different surfactants and fuels and apply it as photoelectrodes. The characterization by infrared spectroscopy and Raman spectroscopy showed that all samples showed characteristic bands of the monoclinic structure BiVO{sub 4}. The samples synthesized with glycine and glycine/Tween® 80 had V{sub 2}O{sub 5}. The film obtained from the alanine/ Tween® 80 showed highest photocurrent values, which may be related to smaller size particles (200 to 300 nm) observed by scanning electron microscopy images. The films obtained using alanine showed highest values of rate constant reaction and percentage discoloration of methylene blue. (author)

  5. Combustion synthesis of red emitting borate host PDP phosphor YCaBO4: Eu3+

    International Nuclear Information System (INIS)

    Ingle, J.T.; Hargunani, S.P.; Sonekar, R.P.; Nagpure, P.A.; Omanwar, S.K.; Moharil, S.V.

    2012-01-01

    The red emitting borate host phosphor YCaBO 4 : Eu 3+ has been prepared by a novel solution combustion technique. The synthesis is based on the exothermic reaction between the fuel (Urea) and Oxidizer (Ammonium nitrate). The photoluminescence properties of the powder samples of YCaBO 4 : Eu 3+ has been investigated under UV and VUV excitation. The phosphor shows strong absorption in UV and VUV region and exhibits intense red emission upon excited by 254 nm UV and 173 nm VUV radiation. Under UV 254 nm excitation, YCaBO 4 : Eu 3+ exhibits intense red emission around 610 nm. Under VUV excitation of 173 nm, the phosphor emits intense red emission around 610 nm and few weak emissions. These weak emissions could be suppressed by annealing the sample repeatedly at proper temperature and the borate phosphor YCaBO 4 : Eu 3+ could be a good red emitting phosphor for PDP display and mercury free lamps. (author)

  6. Development and characterization of Mn2+-doped MgO nanoparticles by solution combustion synthesis

    Science.gov (United States)

    Basha, Md. Hussain; Gopal, N. O.; Rao, J. L.; Nagabhushana, H.; Nagabhushana, B. M.; Chakradhar, R. P. S.

    2015-06-01

    Mn doped MgO Nanoparticles have been prepared by Solution Combustion Synthesis. The synthesized sample is characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Electron Paramagnetic Resonance (EPR). The prepared MgO:Mn (1 mol%) nano crystals appear to be of simple cubic crystalline phase with lattice parameters a = 4.218(2) Å and cell volume = 74.98 (7) Å3. SEM micrograph of powders show highly porous, many agglomerates with irregular morphology, large voids, cracks and pores. EPR spectrum of the sample at room temperature exhibit an isotropic sextet hyperfine pattern, centered at g=1.99, characteristic if Mn2+ ions with S=I=5/2.The observed g value and the hyperfine value reveal the ionic bonding between Mn2+ and its surroundings.

  7. Development and characterization of Mn2+-doped MgO nanoparticles by solution combustion synthesis

    International Nuclear Information System (INIS)

    Basha, Md. Hussain; Gopal, N. O.; Rao, J. L.; Nagabhushana, H.; Nagabhushana, B. M.; Chakradhar, R. P. S.

    2015-01-01

    Mn doped MgO Nanoparticles have been prepared by Solution Combustion Synthesis. The synthesized sample is characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Electron Paramagnetic Resonance (EPR). The prepared MgO:Mn (1 mol%) nano crystals appear to be of simple cubic crystalline phase with lattice parameters a = 4.218(2) Å and cell volume = 74.98 (7) Å 3 . SEM micrograph of powders show highly porous, many agglomerates with irregular morphology, large voids, cracks and pores. EPR spectrum of the sample at room temperature exhibit an isotropic sextet hyperfine pattern, centered at g=1.99, characteristic if Mn 2+ ions with S=I=5/2.The observed g value and the hyperfine value reveal the ionic bonding between Mn 2+ and its surroundings

  8. Optical filtering and luminescence property of some molybdates prepared by combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Yadav, P. J., E-mail: yadav.pooja75@yahoo.in [Department of Electronics, RTM Nagpur University, Nagpur (India); Joshi, C. P. [Physics Department, RCOEM, Nagpur (India); Moharil, S. V., E-mail: svmoharil@yahoo.com [Physics Department, RTM Nagpur University, Nagpur (India)

    2014-10-15

    As an important class of lanthanide inorganic compounds, rare earth ions doped molybdates have gained much attention due to their attractive luminescence and structural properties, supporting various promising applications as phosphor materials in the fields such as white light-emitting diodes, optical fibers, biolabel, lasers, and so on. The molybdate family has promising trivalent cation conducting properties and most of the optical properties result from electron transitions of the 4f shell, which are greatly affected by the composition and structures of rare-earth compounds. In this paper we report the molybdate CaMoO{sub 4}:Eu{sup 3+} for red SSL and Bi{sub 1.4}Y{sub 0.6}MoO{sub 6}, Y{sub 6}MoO{sub 12} for optical filtering, prepared by one step combustion synthesis.

  9. Solution combustion method for synthesis of nanostructured hydroxyapatite, fluorapatite and chlorapatite

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Junjie; Dong, Xiaochen; Bian, Mengmeng [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Zhao, Junfeng, E-mail: daidai02304@163.com [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Jiangsu Laboratory of Advanced Functional Materials, Changshu Institute of Technology, Changshu (China); Zhang, Yao; Sun, Yue [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Chen, JianHua; Wang, XuHong [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Jiangsu Laboratory of Advanced Functional Materials, Changshu Institute of Technology, Changshu (China)

    2014-09-30

    Highlights: • We report a synthesis of HA, Fap and Clap vio a modified solution combustion method. The nucleation of β-TCP was inhibited in the abundant-calcium system (Ca/P = 2.3>>1.67) in this study. F{sup −} brushed into the structure of HA and replace the position of OH{sup −} is easier than that of Cl{sup −}. - Abstract: Hydroxyapatite (HAP), fluorapatite (Fap) and chlorapatite (Clap) were prepared by solution combustion method with further annealing at 800 °C. The characterization and structural features of the synthesized powders were evaluated by the powder X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM) and transmission electron microscopy (TEM) techniques. Characterization results from XRD and Rietveld analysis revealed that OH{sup −} in the HAP lattice were gradually substituted with the increase of F{sup −} and Cl{sup −} content and totally substituted at the molar concentration of 0.28 and 0.6, respectively. The results from FI-IR have also confirmed the incorporation of substituted anions in the apatite structure.

  10. Combustion synthesis by reaction and characterization of structural Ni-Zn ferrite doped with copper

    International Nuclear Information System (INIS)

    Dantas, J.; Santos, J.R.D.; Cunha, R.B.L.; Feitosa, C.A.; Costa, A.C.F.M.

    2012-01-01

    The present stud aims to evaluate the effect of doping with Cu 2+ ions concentrations of 0.0, 0.1, 0.2, 0.3 and 0.4 mol in the synthesis and structure of Ni-Zn ferrite. Samples were synthesized by the method of the combustion reaction and characterized by measuring the temperature as a function of reaction time, X-ray diffraction (XRD) and infrared spectroscopy in Fourier transform (FTIR). The combustion temperature and time were 646, 900, 989, 975 and 735°C and 210, 175, 220, 210 and 110 seconds for the sample doped with 0.0, 0.1, 0.2, 0.3 and 0.4 mol of copper, respectively. XRD results show that all concentrations of copper evaluated, there was only a training phase inverse spinel ferrite and Ni-Zn FTIR spectra show absorption bands below 1000cm -1 , which are characteristics of the spinel type AB 2 O 4- (author)

  11. Mechanically activated combustion synthesis of molybdenum borosilicides for ultrahigh-temperature structural applications

    Energy Technology Data Exchange (ETDEWEB)

    Esparza, Alan A.; Shafirovich, Evgeny, E-mail: eshafirovich2@utep.edu

    2016-06-15

    The thermal efficiency of gas-turbine power plants could be dramatically increased by the development of new structural materials based on molybdenum silicides and borosilicides, which can operate at temperatures higher than 1300 °C with no need for cooling. A major challenge, however, is to simultaneously achieve high oxidation resistance and acceptable mechanical properties at high temperatures. Materials based on Mo{sub 5}SiB{sub 2} (called T{sub 2}) phase are promising materials that offer favorable combinations of high temperature mechanical properties and oxidation resistance. In the present paper, T{sub 2} phase based materials have been obtained using mechanically activated self-propagating high-temperature synthesis (MASHS). Upon ignition, Mo/Si/B/Ti mixtures exhibited a self-sustained propagation of a spinning combustion wave, but the products were porous, contained undesired secondary phases, and had low oxidation resistance. The “chemical oven” technique has been successfully employed to fabricate denser and stronger Mo{sub 5}SiB{sub 2}–TiC, Mo{sub 5}SiB{sub 2}–TiB{sub 2}, and Mo–Mo{sub 5}SiB{sub 2}–Mo{sub 3}Si materials. Among them, Mo{sub 5}SiB{sub 2}–TiB{sub 2} material exhibits the best oxidation resistance at temperatures up to 1500 °C. - Highlights: • Mechanical activation has enabled combustion synthesis of Mo{sub 5}SiB{sub 2} based materials. • For the first time, the fabrication of Mo{sub 5}SiB{sub 2}–TiB{sub 2} material has been reported. • Among the obtained materials, Mo{sub 5}SiB{sub 2}–TiB{sub 2} exhibits the best oxidation resistance.

  12. Assessment of the synthesis conditions for nano-Bi_4Ti_3O_1_2 production by the combustion route

    International Nuclear Information System (INIS)

    Dias, Jeferson A.; Nascimento, Cassia C.; Oliveira, Jessica A.; Morelli, Marcio R.

    2016-01-01

    The bismuth titanate has interesting optoelectronic properties. Its production in nanometric scale is important due to the demand of miniaturized electronic devices and greater synthesization facility. This study aims at the evaluation of synthesis parameters for nano-Bi_4Ti_3O_1_2 production by the combustion route. For that, the materials were synthesized and calcined at 600°C, 700°C and 800°C. The materials were posteriorly characterized by X-Ray diffraction, SEM, DSC-TGA, FTIR; DRS and impedance spectroscopy. The results have demonstrated that the combustion method was effective for nanocrystalline powders production, which also showed high levels of purity. Particles size growth was observed for high treatment temperatures. Low level of residual organic matter was determined and the high electrical resistivity was observed. The temperature of 600°C was enough to produce particles with optimal properties. Therefore, the results have confirmed the efficacy of combustion route to produce nanometric Bi_4Ti_3O_1_2. (author)

  13. Testing of the Engineering Model Electrical Power Control Unit for the Fluids and Combustion Facility

    Science.gov (United States)

    Kimnach, Greg L.; Lebron, Ramon C.; Fox, David A.

    1999-01-01

    The John H. Glenn Research Center at Lewis Field (GRC) in Cleveland, OH and the Sundstrand Corporation in Rockford, IL have designed and developed an Engineering Model (EM) Electrical Power Control Unit (EPCU) for the Fluids Combustion Facility, (FCF) experiments to be flown on the International Space Station (ISS). The EPCU will be used as the power interface to the ISS power distribution system for the FCF's space experiments'test and telemetry hardware. Furthermore. it is proposed to be the common power interface for all experiments. The EPCU is a three kilowatt 12OVdc-to-28Vdc converter utilizing three independent Power Converter Units (PCUs), each rated at 1kWe (36Adc @ 28Vdc) which are paralleled and synchronized. Each converter may be fed from one of two ISS power channels. The 28Vdc loads are connected to the EPCU output via 48 solid-state and current-limiting switches, rated at 4Adc each. These switches may be paralleled to supply any given load up to the 108Adc normal operational limit of the paralleled converters. The EPCU was designed in this manner to maximize allocated-power utilization. to shed loads autonomously, to provide fault tolerance. and to provide a flexible power converter and control module to meet various ISS load demands. Tests of the EPCU in the Power Systems Facility testbed at GRC reveal that the overall converted-power efficiency, is approximately 89% with a nominal-input voltage of 12OVdc and a total load in the range of 4O% to 110% rated 28Vdc load. (The PCUs alone have an efficiency of approximately 94.5%). Furthermore, the EM unit passed all flight-qualification level (and beyond) vibration tests, passed ISS EMI (conducted, radiated. and susceptibility) requirements. successfully operated for extended periods in a thermal/vacuum chamber, was integrated with a proto-flight experiment and passed all stability and functional requirements.

  14. Hot gas cleanup test facility for gasification and pressurized combustion. Quarterly technical progress report, July 1--September 30, 1992

    Energy Technology Data Exchange (ETDEWEB)

    1992-12-31

    The objective of this project is to evaluate hot gas particle control technologies using coal-derived gas streams. This will entail the design, construction, installation, and use of a flexible test facility which can operate under realistic gasification and combustion conditions. The major particulate control device issues to be addressed include the integration of the particulate control devices into coal utilization systems, on-line cleaning techniques, chemical and thermal degradation of components, fatigue or structural failures, blinding, collection efficiency as a function of particle size, and scale-up of particulate control systems to commercial size. The conceptual design of the facility was extended to include a within scope, phased expansion of the existing Hot Gas Cleanup Test Facility Cooperative Agreement to also address systems integration issues of hot particulate removal in advanced coal-based power generation systems. This expansion included the consideration of the following modules at the test facility in addition to the existing Transport Reactor gas source and Hot Gas Cleanup Units: Carbonizer/Pressurized Circulating Fluidized Bed Gas Source; hot Gas Cleanup Units to mate to all gas streams; and Combustion Gas Turbine. Fuel Cell and associated gas treatment. This expansion to the Hot Gas Cleanup Test Facility is herein referred to as the Power Systems Development Facility (PSDF).

  15. Reduction of dioxins-furans formed in combustion and Denovo synthesis

    International Nuclear Information System (INIS)

    Teller, A.J.

    1991-01-01

    This paper reports that the acceptance that Denovo synthesis of dioxins and furans occurs on the surface of flyash particles in the temperature range of 200 degrees C-400 degrees C, establishes that post combustion formation of dioxins must be addressed. Dioxin-guran emission reduction can be achieved by addition of synthesis inhibitors, adsorbers, catalytic destruction, or utilization of the inherent capability of silica-alumina for chemisorption of the dioxins and furans within appropriate temperature ranges. The chemisorption procedure, as applied to commercial incinerator operation adds no additional equipment or capital and operating costs to the system. The equilibria rather kinetics controls the absorption. Thus, wide variation in inlets are accepted by the system with no externally induced system response required. Experience at the Commerce, California waste to energy system established reductions of total dioxin and furan cogeners to 1.9 ng/Nm 3 from inlet concentrations ranging from 28 to 735 ng/Mm 3 , within the existing acid gas-particulate-heavy metal removal system, using only temperature control to affect the removal by chemisorption

  16. Facile synthesis of water-soluble curcumin nanocrystals

    Directory of Open Access Journals (Sweden)

    Marković Zoran M.

    2015-01-01

    Full Text Available In this paper, facile synthesis of water soluble curcumin nanocrystals is reported. Solvent exchange method was applied to synthesize curcumin nanocrystals. Different techniques were used to characterize the structural and photophysical properties of curcumin nanocrystals. We found that nanocurcumin prepared by this method had good chemical and physical stability, could be stored in the powder form at room temperature, and was freely dispersible in water. It was established that the size of curcumin nanocrystals was varied in the range of 20-500 nm. Fourier transform infrared spectroscopy and UV-Vis analyses showed the presence of tetrahydrofuran inside the curcumin nanocrystals. Also, it was found that nanocurcumin emitted photoluminescencewith yellow-green colour. [Projekat Ministarstva nauke Republike Srbije, br. 172003

  17. Combustion synthesis and photoluminescence in novel red emitting yttrium gadolinium pyrosilicate nanocrystalline phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Hedaoo, V.P., E-mail: vraikwar@rediffmail.com [Department of Physics, R. J. College, Ghatkopar, Mumbai, MS 400086 (India); Bhatkar, V.B. [Department of Physics, Shri Shivaji Science College, Amravati, MS 444602 (India); Omanwar, S.K. [Department of Physics, SGB Amravati University, Amravati, MS 444602 (India)

    2016-07-05

    Yttrium Gadolinium Pyrosilicate Y{sub 2-x}Gd{sub x}Si{sub 2}O{sub 7}:Eu{sup 3+} (x = 0.05, 0.10, 0.15) phosphor powder was prepared by facile and time efficient modified combustion method for the first time. The phosphor was characterized by powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), photoluminescence excitation (PLE) and emission (PL) spectroscopy and color chromaticity coordinates. XRD revealed the monoclinic crystal structure with space group P1¯. The crystallite size was calculated by Williamson-Hall (W–H) analysis. Nanoplates-like morphology was observed in FESEM analysis with size in the range 50–80 nm. TEM images confirmed the particle size and shape. Upon excitation by 254 nm UV light, the phosphor showed the characteristic red emission peaks at 589 nm and 613 nm corresponding to {sup 5}D{sub 0} → {sup 7}F{sub 1} and {sup 5}D{sub 0} → {sup 7}F{sub 2} transitions respectively. It was observed that the nanocrystalline phosphor Y{sub 2-x}Gd{sub x}Si{sub 2}O{sub 7}:Eu{sup 3+}can be tuned to emit orange to red color by adjusting the ratio Y/Gd. This phosphor thus can be a potential candidate as orange to red color emitting tunable nanocrystalline phosphor for optical devices. - Highlights: • A novel Yttrium Gadolinium Pyrosilicate doped with Eu{sup 3+} is reported. • Facile and time efficient modified combustion method is used. • The nanocrystalline structure was shown by X-ray diffraction, W–H analysis. • FESEM and TEM images confirmed the nanocrystalline structure. • The reported phosphor can be tuned from orange to red by varying Y/Gd ratio.

  18. Dry sorbent injection of trona to control acid gases from a pilot-scale coal-fired combustion facility

    Directory of Open Access Journals (Sweden)

    Tiffany L. B. Yelverton

    2016-01-01

    Full Text Available  Gaseous and particulate emissions from the combustion of coal have been associated with adverse effects on human and environmental health, and have for that reason been subject to regulation by federal and state governments. Recent regulations by the United States Environmental Protection Agency have further restricted the emissions of acid gases from electricity generating facilities and other industrial facilities, and upcoming deadlines are forcing industry to consider both pre- and post-combustion controls to maintain compliance. As a result of these recent regulations, dry sorbent injection of trona to remove acid gas emissions (e.g. HCl, SO2, and NOx from coal combustion, specifically 90% removal of HCl, was the focus of the current investigation. Along with the measurement of HCl, SO2, and NOx, measurements of particulate matter (PM, elemental (EC, and organic carbon (OC were also accomplished on a pilot-scale coal-fired combustion facility. Gaseous and particulate emissions from a coal-fired combustor burning bituminous coal and using dry sorbent injection were the focus of the current study. From this investigation it was shown that high levels of trona were needed to achieve the goal of 90% HCl removal, but with this increased level of trona injection the ESP and BH were still able to achieve greater than 95% fine PM control. In addition to emissions reported, measurement of acid gases by standard EPA methods were compared to those of an infrared multi-component gas analyzer. This comparison revealed good correlation for emissions of HCl and SO2, but poor correlation in the measurement of NOx emissions.

  19. Mechanically Activated Combustion Synthesis of MoSi2-Based Composites

    Energy Technology Data Exchange (ETDEWEB)

    Shafirovich, Evgeny [Univ. of Texas, El Paso, TX (United States)

    2015-09-30

    The thermal efficiency of gas-turbine power plants could be dramatically increased by the development of new structural materials based on molybdenum silicides and borosilicides, which can operate at temperatures higher than 1300 °C with no need for cooling. A major challenge, however, is to simultaneously achieve high oxidation resistance and acceptable mechanical properties at high temperatures. One approach is based on the fabrication of MoSi2-Mo5Si3 composites that combine high oxidation resistance of MoSi2 and good mechanical properties of Mo5Si3. Another approach involves the addition of boron to Mo-rich silicides for improving their oxidation resistance through the formation of a borosilicate surface layer. In particular, materials based on Mo5SiB2 phase are promising materials that offer favorable combinations of high temperature mechanical properties and oxidation resistance. However, the synthesis of Mo-Si-B multi-phase alloys is difficult because of their extremely high melting temperatures. Mechanical alloying has been considered as a promising method, but it requires long milling times, leading to large energy consumption and contamination of the product by grinding media. In the reported work, MoSi2-Mo5Si3 composites and several materials based on Mo5SiB2 phase have been obtained by mechanically activated self-propagating high-temperature synthesis (MASHS). Short-term milling of Mo/Si mixture in a planetary mill has enabled a self-sustained propagation of the combustion front over the mixture pellet, leading to the formation of MoSi2-T1 composites. Combustion of Mo/Si/B mixtures for the formation of T2 phase becomes possible if the composition is designed for the addition of more exothermic reactions leading to the formation of MoB, TiC, or TiB2. Upon ignition, Mo/Si/B and Mo/Si/B/Ti mixtures exhibited spin combustion, but the products were porous, contained undesired secondary phases, and had low oxidation resistance. It has been shown that use of

  20. Facile synthesis of degradable and electrically conductive polysaccharide hydrogels.

    Science.gov (United States)

    Guo, Baolin; Finne-Wistrand, Anna; Albertsson, Ann-Christine

    2011-07-11

    Degradable and electrically conductive polysaccharide hydrogels (DECPHs) have been synthesized by functionalizing polysaccharide with conductive aniline oligomers. DECPHs based on chitosan (CS), aniline tetramer (AT), and glutaraldehyde were obtained by a facile one-pot reaction by using the amine group of CS and AT under mild conditions, which avoids the multistep reactions and tedious purification involved in the synthesis of degradable conductive hydrogels in our previous work. Interestingly, these one-pot hydrogels possess good film-forming properties, electrical conductivity, and a pH-sensitive swelling behavior. The chemical structure and morphology before and after swelling of the hydrogels were verified by FT-IR, NMR, and SEM. The conductivity of the hydrogels was tuned by adjusting the content of AT. The swelling ratio of the hydrogels was altered by the content of tetraaniline and cross-linker. The hydrogels underwent slow degradation in a buffer solution. The hydrogels obtained by this facile approach provide new possibilities in biomedical applications, for example, biodegradable conductive hydrogels, films, and scaffolds for cardiovascular tissue engineering and controlled drug delivery.

  1. Combustion behaviour and deposition characteristics of Cynara Cardunculus/Greek lignite co-firing under various thermal shares in a thermal pilot-scale facility

    Energy Technology Data Exchange (ETDEWEB)

    Fuller, Aaron; Maier, Joerg; Scheffknecht, Guenter [Stuttgart Univ. (Germany). Inst. of Combustion and Power Plant Technology; Pawlak-Kruczek, Halina [Wroclaw Univ. of Technology (Poland). Inst. of Heat Engineering and Fluid Mechanics; Karampinis, Emmanouil; Grammelis, Panagiotis; Kakaras, Emmanuel [Centre for Research and Technology Hellas, Ptolemais (Greece). Chemical Process and Energy Resources Inst.; National Technical Univ. of Athens (Greece). Lab. of Steam Boilers and Thermal Plants

    2013-06-01

    The combustion of herbaceous biomass in industrial boilers, either as co-firing fuel or in dedicated combustion units, possess significant operating challenges due to increased risks for corrosion and slagging/fouling. The present work aims at investigating the combustion behaviour of Cynara Cardunculus (cardoon) in a range of thermal shares (0 to 100 %) with a Greek lignite. Combustion tests were performed in a 0.5 MW thermal input pulverised fuel pilot-scale test facility. Deposits were characterised in terms of morphological and ash fusion behaviour, and slagging/fouling tendencies were determined. (orig.)

  2. Preparation of MoB and MoB-MoSi2 composites by combustion synthesis in SHS mode

    International Nuclear Information System (INIS)

    Yeh, C.L.; Hsu, W.S.

    2007-01-01

    Combustion synthesis in the mode of self-propagating high-temperature synthesis (SHS) was carried out in the Mo-B and Mo-B-Si systems for the preparation of molybdenum boride MoB and the composite of MoB-MoSi 2 from elemental powder compacts. Under a preheating temperature above 150 deg. C , the reaction of Mo with boron in the sample compact of Mo:B = 1:1 is characterized by a planar combustion front propagating in a self-sustaining and steady manner. As the preheating temperature or sample compaction density increased, combustion temperature was found to increase and the propagation rate of the combustion front was correspondingly enhanced. Moreover, the XRD analysis provides evidence of yielding nearly single-phase α-MoB from the Mo-B sample at equiatomic stoichiometry. In the synthesis of MoB-MoSi 2 composites, the starting stoichiometry of the Mo-B-Si powder compact was varied so as to produce the final composites containing 20-80 mol% MoB. It was also found the increase of flame-front velocity and combustion temperature with increasing MoB content formed in the composite. The composition analysis by XRD shows excellent conversion from the Mo-B-Si powder compact to the MoB-MoSi 2 composite through the SHS reaction; that is, in addition to a small amount of Mo 5 Si 3 , the as-synthesized composite is composed entirely of MoB and MoSi 2

  3. On the formation of Mo{sub 2}C nanocrystals by a novel system through microwave assisted combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Hoseinpur, Arman, E-mail: arman_hoseinpur@metaleng.iust.ac.ir [School of Metallurgy and Materials Engineering, Iran University of Science and Technology (IUST), 16846-13114, Narmak, Tehran, Islamic Republic of Iran (Iran, Islamic Republic of); Jalaly, Maisam [Nanotechnology Department, School of New Technologies, Iran University of Science and Technology (IUST), 16846-13114, Narmak, Tehran, Islamic Republic of Iran (Iran, Islamic Republic of); Bafghi, Mohammad Sh. [School of Metallurgy and Materials Engineering, Iran University of Science and Technology (IUST), 16846-13114, Narmak, Tehran, Islamic Republic of Iran (Iran, Islamic Republic of); Khaki, Jalil Vahdati [Department of Materials Engineering, Ferdowsi University of Mashhad, 91775-1111, Islamic Republic of Iran (Iran, Islamic Republic of)

    2015-10-15

    This research is devoted to microwave assisted combustion synthesis of Mo{sub 2}C nanoparticles. The ternary system of MoO{sub 3}–Zn–C was used as a novel approach for the in-situ synthesis of Mo{sub 2}C in which the zincothermic reduction of MoO{sub 3} was responsible for the combustion to take place. Results showed that the formation of Mo{sub 2}C was assisted by the zincothermic reaction, although further microwave heating up to 6 min was necessary to complete the reaction. The effects of the microwave heating and mechanical activation on the reaction progress were investigated. X-ray powder diffraction was used to examine the synthesis progress. Final products (Mo{sub 2}C and ZnO) were successfully separated from each other and the synthesized carbide was characterized by transmission electron microscopy (TEM), showing the formation of Mo{sub 2}C hexagonal nanocrystals during combustion process. - Highlights: • Hexagonal β-Mo{sub 2}C nanocrystals were successfully synthesized. • MoO{sub 3}–Zn–C powder mixture was selected as the initial mixture for the in-situ synthesis of Mo{sub 2}C. • 30 min of mechanical activation was necessary for the carbide formation to be completed. • The zincothermic reduction of MoO{sub 3} by Zn was responsible for the combustion. • The final products included of Mo{sub 2}C and ZnO in which ZnO was removed by acid leaching.

  4. Auto-combustion synthesis and characterization of Mg doped CuAlO{sub 2} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Agrawal, Shraddha, E-mail: shraddhaa32@gmail.com; Parveen, Azra; Naqvi, A. H. [Centre of Excellence in Materials Science (Nanomaterials), Department of Applied Physics, Z.H. College of Engg.& Technology, Aligarh Muslim University, Aligarh-202002 (India)

    2015-06-24

    The synthesis of pure and Mg doped Copper aluminumoxide CuAlO{sub 2}nanoparticles, a promising p-type TCO (transparent conducting oxide) have been done bysol gel auto combustion method using NaOH as a fuel, calcinated at 600°C. The structural properties were examined by XRD and SEM techniques. The optical absorption spectra of CuAlO{sub 2} sample recorded by UV-VIS spectrophotometer in the range of 200 to 800 nm have been presented. The crystallite size was determined by powder X-ray diffraction technique. The electrical behavior of pure and Mg doped CuAlO{sub 2} has been studied over a wide range of frequencies by using complex impedance spectroscopy.The variation of a.c. conductivity has been studied as function of frequency and temperature. The data taken together conclude that doping causes decreases in the ac conductivity of the nanoparticles as compared with the pure nanoparticles. Mg doping affects the optical properties and band gap.

  5. Combustion synthesis of CoCrMo orthopedic implant alloys: microstructure and properties

    International Nuclear Information System (INIS)

    Li, Bingyun; Mukasyan, Alexander; Varma, Arvind

    2003-01-01

    Because of their excellent properties, such as corrosion resistance, fatigue strength and biocompatibility, cobalt-based alloys are widely used in total hip and knee replacements, dental devices and support structures for heart valves. In this work, CoCrMo alloys were synthesized using a novel method based on combustion synthesis (CS), an advanced technique to produce a wide variety of materials including alloys and near-net shape articles. This method possesses several advantages over conventional processes, such as low energy requirements, short processing times and simple equipment. The evaluated material properties included density and yield measurements, composition and microstructure analysis, hardness, friction and tensile tests. It was shown that microstructure of CS-material is finer and more uniform as compared to the conventional standard. It was also found that among various additives, Cr 3 C 2 is the most effective one for increasing material hardness. In addition, synthesized CoCrMo alloys exhibited good friction and mechanical properties. (orig.)

  6. Solution Combustion Preparation Of Nano-Al2O3: Synthesis and Characterization

    Directory of Open Access Journals (Sweden)

    M. Farahmandjou

    2015-06-01

    Full Text Available The aluminum oxide materials are widely used in ceramics, refractories and abrasives due to their hardness, chemical inertness, high melting point, non-volatility and resistance to oxidation and corrosion. The paper describes work done on synthesis of α-alumina by using the simple, non-expensive solution combustion method using glycine as fuel.Aluminum oxide (Al2O3 nanoparticles were synthesized by aluminum nitrate 9-hydrate as precursor and glycine as fuel. The samples were characterized by high resolution transmission electron microscopy (HRTEM, field effect scanning electron microscopy (FESEM, X-ray diffraction (XRD and electron dispersive spectroscopy (EDS. As there are many forms of transition aluminas produced during this process, x-ray diffraction (XRD technique was used to identify α-alumina. The diameter of sphere-like as-prepared nanoparticles was about 10 nm as estimated by XRD technique and direct HRTEM observation. The surface morphological studies from SEM depicted the size of alumina decreases with increasing annealing temperature. Absorbance peak of UV-Vis spectrum showed the small bandgap energy of 2.65 ev and the bandgap energy increased with increasing annealing temperature because of reducing the size.

  7. Low-reactive circulating fluidized bed combustion (CFBC) fly ashes as source material for geopolymer synthesis

    International Nuclear Information System (INIS)

    Xu Hui; Li Qin; Shen Lifeng; Zhang Mengqun; Zhai Jianping

    2010-01-01

    In this contribution, low-reactive circulating fluidized bed combustion (CFBC) fly ashes (CFAs) have firstly been utilized as a source material for geopolymer synthesis. An alkali fusion process was employed to promote the dissolution of Si and Al species from the CFAs, and thus to enhance the reactivity of the ashes. A high-reactive metakaolin (MK) was also used to consume the excess alkali needed for the fusion. Reactivities of the CFAs and MK were examined by a series of dissolution tests in sodium hydroxide solutions. Geopolymer samples were prepared by alkali activation of the source materials using a sodium silicate solution as the activator. The synthesized products were characterized by mechanical testing, scanning electron microscopy (SEM), X-ray diffractography (XRD), as well as Fourier transform infrared spectroscopy (FTIR). The results of this study indicate that, via enhancing the reactivity by alkali fusion and balancing the Na/Al ratio by additional aluminosilicate source, low-reactive CFAs could also be recycled as an alternative source material for geopolymer production.

  8. Self-ignition combustion synthesis of TiFe in hydrogen atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Wakabayashi, R. [Center for Advanced Research of Energy Conversion Materials, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan)], E-mail: ryuta@eng.hokudai.ac.jp; Sasaki, S. [Center for Advanced Research of Energy Conversion Materials, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan); Saita, I. [National Institute of Advanced Industrial Science and Technology (AIST), AIST Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565 (Japan); Sato, M. [Center for Advanced Research of Energy Conversion Materials, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan); Uesugi, H. [Bio Coke Lab., Ltd., 5-34-20 Hirato, Totsuka-ku, Yokohama, Kanagawa 244-0802 (Japan); Akiyama, T. [Center for Advanced Research of Energy Conversion Materials, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan)

    2009-07-08

    This paper describes the self-ignition combustion synthesis (SICS) of highly active titanium iron (TiFe) in a high-pressure hydrogen atmosphere without employing an activation process. In the experiments, well-mixed powders of Ti and Fe in the molar ratio of 1:1 were uniformly heated up to 1085 deg. C, the eutectic temperature of Ti-Fe binary system, in pressurized hydrogen at 0.9 MPa. The electric source was disconnected immediately after the ignition between Ti and Fe, and the mixture was cooled naturally. In this study, the exothermic reaction Ti + Fe = TiFe + 40 kJ occurred at around 1085 deg. C after the hydrogenation and decomposition of Ti. X-ray diffraction analysis showed that the final product had only one phase-TiFeH{sub 0.06}-which can store hydrogen of 1.55 mass% under hydrogen pressure of 4 MPa. The product obtained by SICS contained considerably more hydrogen quickly as compared to the commercially available product; this fact can be explained by the porous structure of the obtained product, which was observed using a scanning electron microscope. In conclusion, the SICS of TiFe saved time and energy, yields products with high porosity and small crystals, enabled easy hydrogenation, and did not require activation processes.

  9. MgAl_2O_4 foams obtained by combustion synthesis

    International Nuclear Information System (INIS)

    Moraes, G.G.; Rosa, M.A.; Kronbauer, D.P.; Pozzobom, I.F.; Fernandes, C.P.; Oliveira, A.P. Novaes de

    2014-01-01

    This work aims to study magnesium aluminate (MgAl_2O_4) ceramic foams obtained by combustion synthesis in solution without the need of surfactants to stabilize bubbles. The precursors, Al(NO_3)_3_.9H_2O and Mg(NO_3)_2_.6H_2_O, dispersed in distilled water (20 wt%) were magnetically stirred under heating (70°C). At the beginning of the reaction, a fuel composed by a mixture of residual glycerins from the production of biodiesel was added. The foams were produced by controlling the stirring speed and temperature. The applied thermal cycle to consolidate the foams consisted of heating at 1°C/min to 600°C/120 min and subsequently raising the temperature at 10°C/min to 1600°C/120 min. The obtained materials were characterized by SEM,TEM and from tomographic images. The results showed that the obtained magnesium aluminate foams have a high porosity (97%), a high connectivity and pore sizes (diameters) between 30 and 1200 μm. (author)

  10. Thermoluminescence study of aluminium oxide doped germanium prepared by combustion synthesis method

    Directory of Open Access Journals (Sweden)

    Saharin Nurul Syazlin Binti

    2017-01-01

    Full Text Available The present paper reports the optimum concentration of germanium (Ge dopant in aluminium oxide (AhO3 samples prepared by combustion synthesis (CS method for thermoluminescence (TL studies. The samples were prepared at various Ge concentration i.e. 1 to 5% mol. The phase formation of un-doped and Ge-doped Al2O3 samples was determined using X-ray Diffraction (XRD. The sharp peaks present in the XRD pattern confirms the crystallinity of the samples. The samples were then exposed to 50 Gy Cobalt-60 sources (Gamma cell 220. TL glow curves were measured and recorded using a Harshaw Model 3500 TLD reader. Comparison of TL peaks were observed to obtain the best composition of Ge dopants. A simple glow curves TL peak at around 175̊C for all composition samples was observed. It was also found that the composition of aluminium oxide doped with 3.0% of germanium exhibits the highest thermoluminescence (TL intensity which is 349747.04 (a.u.

  11. YAG:Dy – Based single white light emitting phosphor produced by solution combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Carreira, J.F.C., E-mail: correiacarreira@ua.pt; Sedrine, N. Ben; Monteiro, T.; Rino, L.

    2017-03-15

    Dysprosium-doped yttrium aluminum garnet (YAG:Dy) phosphor was successfully produced by a Solution Combustion Synthesis (SCS) using a mixture of two fuels (urea and glycine). The effects of Dy concentration and annealing temperature were studied by X-ray diffraction (XRD), Raman spectroscopy (RS), photoluminescence (PL) and photoluminescence excitation (PLE). X-ray diffraction results show that the phosphors are single phase YAG with crystallite size ranging from 45 to 82 nm. Raman spectroscopy corroborates these results and show that the introduction of Dy ions in the YAG lattice results in additional Raman modes. Room temperature photoluminescence results confirm the introduction of the ion in the host lattice and its optical activation for all the Dy concentrations. CIE1931 color coordinates show that the samples’ emission lays in the near white region. The highest intraionic emission intensity was achieved for a Dy concentration of 2 mol% and annealing temperature of 1400 °C. Photoluminescence excitation results show that the ions luminescence is preferential excited with 351.8 and 365.8 nm wavelength photons.

  12. Facile synthesis of chondroitin sulfate-stabilized gold nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Li Wei, E-mail: weilixj8510@163.com [School of Science, Henan Agricultural University, No. 95 Wenhua Road, Zhengzhou, Henan 450002 (China); Li Xin; Su Hui; Zhao Shiju; Li Yanyun; Hu Jiandong [School of Science, Henan Agricultural University, No. 95 Wenhua Road, Zhengzhou, Henan 450002 (China)

    2011-02-15

    A facile and simple method for the synthesis of biocompatible gold nanoparticles (AuNPs) at room temperature has been developed by using sodium borohydride as the reducing agent and employing an inexpensive water-soluble chondroitin sulfate (CS) biopolymer as the stabilizing agent. The as-prepared AuNPs were characterized with ultraviolet-visible (UV-vis) spectroscopy and transmission electron microscopy (TEM). Additionally, the stability of AuNPs in aqueous solution was investigated as a function of the electrolyte sodium chloride concentration. The experimental results showed that even high sodium chloride concentration (1 M) also did not destabilize the colloidal gold solution. So it could be speculated that the high stability of AuNPs should be attributed to the electrostatic repulsion and steric hindrance between the AuNPs stabilized by CS molecules, which wrapped around the surface of as-prepared AuNPs and prevented their agglomeration, and simultaneously improve biocompatibility of AuNPs as well.

  13. Facile synthesis of chondroitin sulfate-stabilized gold nanoparticles

    International Nuclear Information System (INIS)

    Li Wei; Li Xin; Su Hui; Zhao Shiju; Li Yanyun; Hu Jiandong

    2011-01-01

    A facile and simple method for the synthesis of biocompatible gold nanoparticles (AuNPs) at room temperature has been developed by using sodium borohydride as the reducing agent and employing an inexpensive water-soluble chondroitin sulfate (CS) biopolymer as the stabilizing agent. The as-prepared AuNPs were characterized with ultraviolet-visible (UV-vis) spectroscopy and transmission electron microscopy (TEM). Additionally, the stability of AuNPs in aqueous solution was investigated as a function of the electrolyte sodium chloride concentration. The experimental results showed that even high sodium chloride concentration (1 M) also did not destabilize the colloidal gold solution. So it could be speculated that the high stability of AuNPs should be attributed to the electrostatic repulsion and steric hindrance between the AuNPs stabilized by CS molecules, which wrapped around the surface of as-prepared AuNPs and prevented their agglomeration, and simultaneously improve biocompatibility of AuNPs as well.

  14. Ash Deposit Formation and Deposit Properties. A Comprehensive Summary of Research Conducted at Sandia's Combustion Research Facility

    Energy Technology Data Exchange (ETDEWEB)

    Larry L. Baxter

    2000-08-01

    This report summarizes experimental and theoretical work performed at Sandia's Combustion Research Facility over the past eight years on the fate of inorganic material during coal combustion. This work has been done under four broad categories: coal characterization, fly ash formation, ash deposition, and deposit property development. The objective was to provide sufficient understanding of these four areas to be able to predict coal behavior in current and advanced conversion systems. This work has led to new characterization techniques for fuels that provide, for the first time, systematic and species specific information regarding the inorganic material. The transformations of inorganic material during combustion can be described in terms of the net effects of the transformations of these individual species. Deposit formation mechanisms provide a framework for predicting deposition rates for abroad range of particle sizes. Predictions based on these rates many times are quite accurate although there are important exceptions. A rigorous framework for evaluating deposit has been established. Substantial data have been obtained with which to exercise this framework, but this portion of the work is less mature than is any other. Accurate prediction of deposit properties as functions of fuel properties, boiler design, and boiler operating conditions represents the single most critical area where additional research is needed.

  15. Combustion synthesis of CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors in a closed system

    Energy Technology Data Exchange (ETDEWEB)

    Peng Wenfang; Zou Shaoyu; Liu Guanxi; Xiao Quanlan; Zhang Rui; Xie Lijuan; Cao Liwei [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Meng Jianxin, E-mail: tmjx@jnu.edu.cn [Institute of Nano-Chemistry, Jinan University, Guangzhou 510632 (China); Liu Yingliang [Institute of Nano-Chemistry, Jinan University, Guangzhou 510632 (China)

    2011-06-09

    Highlights: > CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors can be prepared by a single-step combustion method. > The ignition temperature is the lowest in the combustion synthesis of Ce{sup 3+}/Eu{sup 2+} doped phosphors. > The as-prepared nano-phosphors give a uniform particle size in the range of 15-20 nm and have highly dispersity and fluorescence intensity. > It is a convenient method for preparation of monodispersed oxide nano-phosphors, especially those being sensitive to air at high temperature. - Abstract: The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors were successfully prepared by a single-step combustion method at an ignition temperature as low as 200 deg. C in a closed autoclave using glycine as a fuel and PEG4000 as a dispersant. The samples were characterized by X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscope (TEM). The results revealed that CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors can be conveniently prepared at an ignition temperature as low as 200 deg. C, which was much lower than that in the ordinary combustion methods. The optimized ignition temperature was 220 deg. C. The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors give a uniform particle size in the range of 15-20 nm. The low ignition temperature and the addition of PEG4000 dispersant play important roles in the formation of small sized nanoparticles. The as-prepared nano-phosphors were incompact aggregates, but highly dispersed nano-phosphors can be obtained after further ultrasonic treatment. The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors give satisfactory luminescence characteristic benefiting from the closed circumstance, in which cerium atoms can be isolated from the oxidizing atmosphere and non-fluorescent Ce{sup 4+} ions can be ruled out. The present highly dispersed CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors with efficient fluorescence are promising in the field of biological labeling

  16. Thermoluminescent dosimetric properties of CaF{sub 2}:Tm produced by combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Vasconcelos, D.A.A. de; Khoury, H.J.; Asfora, V.K.; Barros, V.S.M. [Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil). Dept. de Energia Nuclear; Oliveira, R.A.P. [Universidade Federal do Vale do Sao Francisco (IPCM/UNIVASF), Juazeiro, BA (Brazil). Instituto de Pesquisa em Ciencias dos Materiais. Departamento de Energia Nuclear

    2015-07-01

    Calcium Fluoride is one of the oldest known thermoluminescent materials and is considered to be one of the most sensitive. In particular for thulium doped CaF{sub 2}, since it was introduced in 1977 by Lucas and Kapsar, besides gamma radiation dosimetry, there have been several attempts for its use in application involving mixed radiation fields (ex.: neutron and gamma; alpha and beta), low energy photons, π- dosimetry and neutrino detection. Research for novel improved methods of fabrication are ongoing. This work presents the dosimetric properties results of CaF{sub 2}:Tm produced by combustion synthesis. The X-ray diffraction (Brucker D2 Phaser) confirmed that CaF{sub 2} was successfully produced. Samples were irradiated in a Co-60 (Gammacell 220 Nordion) and Cs-137 (STS/OB-85) gamma sources for high and low doses, respectively. TL emission spectra, obtained using a Hammamatsu optical spectrometer, has the same lines of commercial CaF{sub 2}:Tm, although transitions {sup 3}P{sub 0} → {sup 3}F{sub 4} (455 nm) and {sup 1}G{sub 4}→ {sup 3}H{sub 6} (482 nm) are shown to be proportionally more intense. The dose response lower limit is in the range of 100 μGy. Thermoluminescence glow curves were obtained in a Harshaw 3500 TL reader. The deconvolution technique was employed and seven glow peaks were found as well as its kinetic parameters, similar to the commercial CaF{sub 2}:Tm. A linear dose response curve was obtained for the range 0.1 mGy to 50 Gy, with the onset of a supralinear behavior at 50 Gy up to 100 Gy. The minimum measurable dose for gamma (Cs- 137) was around 100 μGy for a 6.0 mm diameter by 1.0 mm in thickness pellet. Variation of the dose response due to fading was within 6% in 60 days. (author)

  17. Thermoluminescence study of Mn doped lithium tetraborate powder and pellet samples synthesized by solution combustion synthesis

    International Nuclear Information System (INIS)

    Ozdemir, A.; Yegingil, Z.; Nur, N.; Kurt, K.; Tuken, T.; Depci, T.; Tansug, G.; Altunal, V.; Guckan, V.; Sigircik, G.; Yu, Y.; Karatasli, M.; Dolek, Y.

    2016-01-01

    In this paper, the thermoluminescence (TL) dosimetric characteristics under beta-ray, x-ray and gamma-ray excitations of powder and pellet Mn-doped lithium tetraborates (LTB) which were produced by solution combustion synthesis technique were investigated, and the results were compared with that of TLD-100 chips. The chemical composition and morphologies of the obtained LTB and Mn-doped LTB (LTB:Mn) were confirmed by X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) and scanning electron microscopy (SEM) with EDX. LTB:Mn was studied using luminescence spectroscopy. In addition, the effects of sintering and annealing temperatures and times on the thermoluminescence (TL) properties of LTB:Mn were investigated. The glow curves of powder samples as well as pellet samples exposed to different beta doses exhibited a low temperature peak at about 100 °C followed by an intense principal high temperature peak at about 260 °C. The kinetic parameters (E, b, s) associated with the prominent glow peaks were estimated using T m –T stop , initial rise (IR) and computerized glow curve deconvolution (CGCD) methods. The TL response of integral TL output increased linearly with increasing the dose in the range of 0.1–10 Gy and was followed by a superlinearity up to 100 Gy both for powder and pellet samples using beta-rays. Powder and pellet LTB:Mn were irradiated to a known dose by a linear accelerator with 6 and 18 MV photon beams, 6–15 MeV electron beams and a traceable 137 Cs beam to investigate energy response. Further, TL sensitivity, fading properties and recycling effects related with beta exposure of LTB:Mn phosphor were evaluated and its relative energy response was also compared with that of TLD-100 chips. The comparison of the results showed that the obtained phosphors have good TL dose response with adequate sensitivity and linearity for the measurement of medical doses.

  18. Effects of Fuel to Synthesis of CaTiO3 by Solution Combustion Synthesis for High-Level Nuclear Waste Ceramics.

    Science.gov (United States)

    Jung, Choong-Hwan; Kim, Yeon-Ku; Han, Young-Min; Lee, Sang-Jin

    2016-02-01

    A solution combustion process for the synthesis of perovskite (CaTiO3) powders is described. Perovskite is one of the crystalline host matrics for the disposal of high-level radioactive wastes (HLW) because it immobilizes Sr and Lns elements by forming solid solutions. Solution combustion synthesis, which is a self-sustaining oxi-reduction reaction between nitrate and organic fuel, the exothermic reaction, and the heat evolved convert the precursors into their corresponding oxide products above 1100 degrees C in air. To investigate the effects of amino acid on the combustion reaction, various types of fuels were used; a glycine, amine and carboxylic ligand mixture. Sr, La and Gd-nitrate with equivalent amounts of up to 20% of CaTiO3 were mixed with Ca and Ti nitrate and amino acid. X-ray diffraction analysis, SEM and TEM were conducted to confirm the formed phases and morphologies. While powders with an uncontrolled shape are obtained through a general oxide-route process, Ca(Sr, Lns)TiO3 powders with micro-sized soft agglomerates consisting of nano-sized primary particles can be prepared using this method.

  19. Direct Energy Supply to the Reaction Mixture during Microwave-Assisted Hydrothermal and Combustion Synthesis of Inorganic Materials

    Directory of Open Access Journals (Sweden)

    Roberto Rosa

    2014-05-01

    Full Text Available The use of microwaves to perform inorganic synthesis allows the direct transfer of electromagnetic energy inside the reaction mixture, independently of the temperature manifested therein. The conversion of microwave (MW radiation into heat is useful in overcoming the activation energy barriers associated with chemical transformations, but the use of microwaves can be further extended to higher temperatures, thus creating unusual high-energy environments. In devising synthetic methodologies to engineered nanomaterials, hydrothermal synthesis and solution combustion synthesis can be used as reference systems to illustrate effects related to microwave irradiation. In the first case, energy is transferred to the entire reaction volume, causing a homogeneous temperature rise within a closed vessel in a few minutes, hence assuring uniform crystal growth at the nanometer scale. In the second case, strong exothermic combustion syntheses can benefit from the application of microwaves to convey energy to the reaction not only during the ignition step, but also while it is occurring and even after its completion. In both approaches, however, the direct interaction of microwaves with the reaction mixture can lead to practically gradient-less heating profiles, on the basis of which the main observed characteristics and properties of the aforementioned reactions and products can be explained.

  20. Combustion synthesis of AlB2-Al2O3 composite powders with AlB2 nanowire structures

    Science.gov (United States)

    Yang, Pan; Xiao, Guoqing; Ding, Donghai; Ren, Yun; Yang, Shoulei; Lv, Lihua; Hou, Xing

    2018-05-01

    Using of Al and B2O3 powders as starting materials, and Mg-Al alloy as additives, AlB2-Al2O3 composite powders with AlB2 nanowire structures were successfully fabricated via combustion synthesis method in Ar atmosphere at a pressure of 1.5 MPa. The effect of different amount of Mg-Al alloy on the phase compositions and morphology of the combustion products was investigated. The results revealed that AlB2 and Al2O3 increased, whereas Al decreased with the content of Mg-Al alloy increasing. The impurities MgAl2O4 and AlB12 would exist in the sample with adding of 18 wt% Mg-Al alloy. Interestingly, FESEM/TEM/EDS results showed that AlB2 nanowires were observed in the products when the content of Mg-Al alloy is 6 wt% and 12 wt%. The more AlB2 nanowires can be found as the content of Mg-Al alloy increased. And the yield of AlB2 nanowires with the diameter of about 200 nanometers (nm) and the length up to several tens of micrometers (μm) in the combustion product is highest when the content of Mg-Al alloy is 12 wt%. The vapor, such as Mg-Al (g), B2O2 (g), AlO (g) and Al2O (g), produced during the process of combustion synthesis, reacted with each other to yield AlB2 nanowires by vapor-solid (VS) mechanism and the corresponding model was also proposed.

  1. Incineration facility for combustible solid and liquid radioactive wastes in IPEN-CNEN - Sao Paulo

    International Nuclear Information System (INIS)

    Krutman, I.; Grosche Filho, C.E.; Chandra, U.; Suarez, A.A.

    1987-01-01

    A system for incinerating the combustible solid and liquid radioactive wastes was developed in order to achieve higher mass and volume reduction of the wastes generated at IPEN-CNEN/SP or received from other institutions. The radioactive wastes for incineration are: animal carcasses, ion-exchange resins, contaminated lubricant oils, cellulosic materials, plastics, etc. The optimization of the process was achieved by considering the following factors: selection of better construction and insulating material; dimensions; modular design of combustion chambers to increase burning capacity in future; applicability for various types of wastes; choise of gas cleaning system. The off-gas system utilizes dry treatment. The operation is designed to function with a negative pressure. (Author) [pt

  2. New class of combustion processes

    International Nuclear Information System (INIS)

    Merzhanov, A.G.; Borovinskaya, I.P.

    1975-01-01

    A short review is given of the results of work carried out since 1967 on studying the combustion processes caused by the interaction of chemical elements in the condensed phase and leading to the formation of refractory compounds. New phenomena and processes are described which are revealed when investigating the combustion of the systems of this class, viz solid-phase combustion, fast combustion in the condensed phase, filtering combustion, combustion in liquid nitrogen, spinning combustion, self-oscillating combustion, and repeated combustion. A new direction in employment of combustion processes is discussed, viz. a self-propagating high-temperature synthesis of refractory nitrides, carbides, borides, silicides and other compounds

  3. Comparison of Diesel Spray Combustion in Different High-temperature, High-pressure Facilities

    DEFF Research Database (Denmark)

    Pickett, Lyle M.; Genzale, Caroline L.; Bruneaux, Gilles

    2010-01-01

    Diesel spray experimentation at controlled high-temperature and high-pressure conditions is intended to provide a more fundamental understanding of diesel combustion than can be achieved in engine experiments. This level of understanding is needed to develop the high-fidelity multi-scale CFD models...... participants in the ECN. Thus, in addition to the presentation of a comparative study, this paper demonstrates steps that are needed for other interested groups to participate in ECN spray research. We expect that this collaborative effort will generate a high-quality dataset to be used for advanced...

  4. Anatomy of an upgraded pulverized coal facility: Combustion modification through flue gas scrubbing

    Energy Technology Data Exchange (ETDEWEB)

    Watts, J.U. [Dept. of Energy, Pittsburgh, PA (United States). Federal Energy Technology Center; Savichky, W.J.; O`Dea, D.T. [New York State Electric and Gas Corp., Binghamton, NY (United States)

    1997-12-31

    Regeneration is a biological term for formation or creating anew. In the case of Milliken station, a species of steam generation (Tangentus coali) regeneration refers to refitting critical systems with the latest technological advances to reduce emissions while maintaining or improving performance. The plant has undergone a series of operations which provided anatomical changes as well as a face lift. Each of the two units were place in suspended animation (outage) to allow these changes to be made. The paper describes the project which includes retrofitting combustion systems, pulverizers, boiler liners, scrubbers, and control room. This retrofit is meant to increase thermal efficiency while reducing the formation of nitrogen oxides.

  5. Solution combustion synthesis of strontium aluminate, SrAl2O4, powders: single-fuel versus fuel-mixture approach.

    Science.gov (United States)

    Ianoş, Robert; Istratie, Roxana; Păcurariu, Cornelia; Lazău, Radu

    2016-01-14

    The solution combustion synthesis of strontium aluminate, SrAl2O4, via the classic single-fuel approach and the modern fuel-mixture approach was investigated in relation to the synthesis conditions, powder properties and thermodynamic aspects. The single-fuel approach (urea or glycine) did not yield SrAl2O4 directly from the combustion reaction. The absence of SrAl2O4 was explained by the low amount of energy released during the combustion process, in spite of the highly negative values of the standard enthalpy of reaction and standard Gibbs free energy. In the case of single-fuel recipes, the maximum combustion temperatures measured by thermal imaging (482 °C - urea, 941 °C - glycine) were much lower than the calculated adiabatic temperatures (1864 °C - urea, 2147 °C - glycine). The fuel-mixture approach (urea and glycine) clearly represented a better option, since (α,β)-SrAl2O4 resulted directly from the combustion reaction. The maximum combustion temperature measured in the case of a urea and glycine fuel mixture was the highest one (1559 °C), which was relatively close to the calculated adiabatic temperature (1930 °C). The addition of a small amount of flux, such as H3BO3, enabled the formation of pure α-SrAl2O4 directly from the combustion reaction.

  6. The E-3 Test Facility at Stennis Space Center: Research and Development Testing for Cryogenic and Storable Propellant Combustion Systems

    Science.gov (United States)

    Pazos, John T.; Chandler, Craig A.; Raines, Nickey G.

    2009-01-01

    This paper will provide the reader a broad overview of the current upgraded capabilities of NASA's John C. Stennis Space Center E-3 Test Facility to perform testing for rocket engine combustion systems and components using liquid and gaseous oxygen, gaseous and liquid methane, gaseous hydrogen, hydrocarbon based fuels, hydrogen peroxide, high pressure water and various inert fluids. Details of propellant system capabilities will be highlighted as well as their application to recent test programs and accomplishments. Data acquisition and control, test monitoring, systems engineering and test processes will be discussed as part of the total capability of E-3 to provide affordable alternatives for subscale to full scale testing for many different requirements in the propulsion community.

  7. Microwave-assisted combustion synthesis of NiAl intermetallics in a single mode applicator: Modeling and optimisation

    International Nuclear Information System (INIS)

    Poli, G.; Sola, R.; Veronesi, P.

    2006-01-01

    The microwave-assisted combustion synthesis of NiAl intermetallics in a single mode applicator has been simulated numerically and performed with the aim of achieving the highest yields, energy efficiency and process reproducibility. The electromagnetic field modeling of the microwave system allowed to chose the proper experimental set-up and the materials more suitable for the application, minimising the reflected power and the risks of arcing. In all the experimental conditions tested, conversions of 3-5 g 1:1 atomic ratio Ni and Al powder compacts into NiAl ranged from 98.7% to 100%, requiring from 30 to 180 s with power from 500 to 1500 W. The optimisation procedure allowed to determine and quantify the effects of the main process variables on the ignition time, the NiAl yields and the specific energy consumption, leading to a fast, reproducible and cost-effective process of microwave-assisted combustion synthesis of NiAl intermetallics

  8. Synthesis, characterisation, luminescence and defect centres in solution combustion synthesised CaZrO3:Tb3+ phosphor

    International Nuclear Information System (INIS)

    Singh, Vijay; Watanabe, S.; Gundu Rao, T.K.; Al-Shamery, Katharina; Haase, Markus; Jho, Young-Dahl

    2012-01-01

    Tb 3+ doped CaZrO 3 has been prepared by an easy solution combustion synthesis method. The combustion derived powder was investigated by X-ray diffraction, Fourier-transform infrared spectrometry and scanning electron microscopy techniques. A room temperature photoluminescence study showed that the phosphors can be efficiently excited by 251 nm light with a weak emission in the blue and orange region and a strong emission in green light region. CaZrO 3 :Tb 3+ exhibits three thermoluminescence (TL) glow peaks at 126 °C, 200 °C and 480 °C. Electron Spin Resonance (ESR) studies were carried out to study the defect centres induced in the phosphor by gamma irradiation and also to identify the centres responsible for the TL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0233 is identified as an O − ion. Centre II with an axial symmetric g-tensor with principal values g ⊥ =1.9986 and g ⊥ =2.0023 is assigned to an F + centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal annealing experiments and this centre (assigned to F + centre) seems to originate from an F centre (oxygen vacancy with two electrons). The F centre and also the F + centre appear to correlate with the observed high temperature TL peak in CaZrO 3 :Tb 3+ phosphor. - Highlights: ► Powder phosphor of CaZrO 3 :Tb 3+ was prepared by an easy solution combustion synthesis method. ► The phosphor exhibits a bright green emission at 545 nm ( 5 D 4 → 7 F 5 ) of the Tb 3+ ion. ► Electron Spin Resonance studies have been carried out to identify the defect centres responsible for the observed thermoluminescence peaks.

  9. Facile microwave synthesis of uniform magnetic nanoparticles with minimal sample processing

    Energy Technology Data Exchange (ETDEWEB)

    Schneider, Thomas, E-mail: tom.schneider@ubc.ca [Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, V6T 1Z3 Canada (Canada); Löwa, Anna; Karagiozov, Stoyan [Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, V6T 1Z3 Canada (Canada); Sprenger, Lisa [Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, V6T 1Z3 Canada (Canada); TU Dresden, Chair of Magnetofluiddynamics, Measuring and Automation Technology, Dresden, 01062 Germany (Germany); Gutiérrez, Lucía [Instituto Universitario de Nanociencia de Aragón (INA), University of Zaragoza, Zaragoza, 50018 Spain (Spain); Esposito, Tullio; Marten, Gernot; Saatchi, Katayoun [Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, V6T 1Z3 Canada (Canada); Häfeli, Urs O., E-mail: urs.hafeli@ubc.ca [Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, V6T 1Z3 Canada (Canada)

    2017-01-01

    We present a simple and rapid method for the synthesis of small magnetic nanoparticles (diameters in the order of 5–20 nm) and narrow size distributions (CV's of 20–40%). The magnetite nanoparticles were synthesized in green solvents within minutes and the saturation magnetization of the particles was tunable by changes in the reaction conditions. We show that this particle synthesis method requires minimal processing steps and we present the successful coating of the particles with reactive bisphosphonates after synthesis without washing or centrifugation. We found minimal batch-to-batch variability and show the scalability of the particle synthesis method. We present a full characterization of the particle properties and believe that this synthesis method holds great promise for facile and rapid generation of magnetic nanoparticles with defined surface coatings for magnetic targeting applications. - Highlights: ●Rapid and facile synthesis of magnetic nanoparticles. ●Microwave synthesis in green solvent. ●Magnetite MNPs with small sizes and high saturation magnetization. ●Tunable particle properties depending on heating duration. ●Scalable MNP synthesis.

  10. Volume reduction of low-level, combustible, transuranic waste at Mound Facility

    International Nuclear Information System (INIS)

    Bond, W.H.; Doty, J.W.; Koenst, J.W. Jr.; Luthy, D.F.

    Low-level combustible waste (<100 nCi per g of waste) generated during plutonium-238 processing is collected and stored in 55-gallon (200-liter) drums. The composition of this waste is approximately 32 wt % paper, 46% plastic, 16% rubber and cloth, and 6% metal. Treatment of this waste is initiated by burning in the Mound Cyclone Incinerator, which consists of a burning chamber, deluge tank, venturi scrubber and blower. During the two years of operating the Cyclone Incinerator, experiments have been performed on particle distribution throughout the system using various mixtures of feed material. Measurements were taken at the incinerator outlet, after the spray tank, and after the venturi scrubber. An average emission of 0.23 g of particles per kg of feed at the venturi outlet was determined. The distribution of chlorine from the combustion of polyvinyl chloride was studied. Analyses of the off-gas and scrubber solution show that approximately 75 wt % of the chlorine was captured by the scrubber solution and approximately 17 wt % remained in the off-gas after the venturi scrubber. Measurements of the amount of NO/sub chi/ present in the off-gas were also made during the chloride studies. An average of approximately 200 ppM NO/sub chi/ was produced during each incineration run. Immobilization of the incinerator ash is being studied with regard to long-term behavior of the product. The immobilization matrix which looks most promising is ash mixed with Portland 1A cement in a 65/35 wt % ash-to-cement ratio. This matrix exhibits good mechanical properties while maintaining a maximum volume reduction

  11. Synthesis of lithium silicates generators of tritium by a modified method of combustion

    International Nuclear Information System (INIS)

    Cruz G, D.

    2003-01-01

    The ceramics of lithium have been proposed as generating materials of tritium through the following reaction: 6 Li + 1 n → 4 He + 3 H . In previous works carried out by Pfeiffer and collaborators, the lithium silicates generators of tritium were prepared using the following methods: reactions of solid state, precipitation and sol-gel synthesis. Although those methods have advantages, it is required of heating at high temperatures (900 C during four hours) to be able to obtain the crystalline compounds. Those products found in these works were diverse crystallization forms of the lithium silicates and of SiO 2 , such as, Li 2 SiO 3 , Li 2 Si 2 0 5 , Li 4 SiO 4 , and quartz (SiO 2 ). The combustion method uses exothermic reactions to take place ceramic compounds. The precursor solutions are mixtures of the nitrate of metal oxidizer and the fuels (urea, glycine, carbohydrazide). However the reported method in the literature, it is not useful to prepare lithium silicates, for what was modified using non oxidizers compounds. The lithium hydroxide (LiOH) and the silicic acid (H 2 SiO 3 ) they were the compounds non oxidizers used, and the urea (CH 4 N 2 O) it was the one fuel. They were carried out two series of experiments; inside the series 1 of experiments are varied the molar ratio of lithium hydroxide and urea (LiOH : H 2 SiO 3 = 1, 2 and 3, LiOH : CH 4 N 2 O = 1, 2, 3, 4 and 5) and the prepared mixtures were taken to one muffle previously preheated to a temperature of 450 C during 5 minutes. In the series 2 of experiments was studied the effect of the temperature and of the washed with distilled water in the prepared samples with the following molar ratios: LiOH : H 2 SiO 3 : CH 4 N 2 O = 1:1:3, 2:1:3, 3:1:3 and 3:1:6, those which were heated to temperatures from 450 C up to 750 C and were washed. The obtained samples were characterized by X-ray diffraction (XRD), Infrared spectroscopy (I S), semiquantitative elemental analysis (EDS) and Thermal gravimetric

  12. Synthesis of lithium silicates by the modified method of combustion. XRD and IR

    International Nuclear Information System (INIS)

    Cruz, D.; Bulbulian, S.

    2002-01-01

    The combustion method is fixed in exothermic reactions for producing ceramic compounds. The precursor solutions are mixtures of metal nitrates and the fuels. This method was modified using non-oxidant compounds as lithium hydroxide and silicide acid and urea as fuel. The precursors were heated during 5 minutes at temperatures between 250 C and 550 C allowing so the mixture combustion. The obtained ceramics were characterized by X-ray diffraction and IR spectroscopy. The sample pollution with carbonates was evaluated and it was found that the presence of these diminish according as increase the calcination temperature. (Author)

  13. Facile one-pot synthesis of functionalized organophosphonate ...

    Indian Academy of Sciences (India)

    WINTEC

    The reaction of phosphorus trichloride with 2,6-diisopropyl phenol in the presence of LiCl under reflux ... on a Perkin Elmer Spectrum One FT–IR spectrometer. Microanalyses were performed on a Thermo Finni- gan (FLASH EA .... 3.1 Synthesis and characterization .... and no other signals corresponding to the formation.

  14. Facile hydrothermal synthesis of CeO2 nanopebbles

    Indian Academy of Sciences (India)

    Administrator

    However, to the best of our knowledge the reports on the synthesis of CeO2 ... The base pressure of the XAS chamber was in the range of 10–8 Pa. A Shimadzu ... scopy was investigated to confirm the crystalline quality of CeO2 nanopebbles.

  15. Facile synthesis and catalytic properties of silver colloidal ...

    Indian Academy of Sciences (India)

    Administrator

    al 2011). Organic thiol compounds, long-chain amines ... synthesis of nanomaterials by mixing with other co- surfactants such ... example, Zhang and co-workers (2006) used SDBS as a capping .... of AgCNPs, we considered that monolayer micelle model could be ... significantly with pH value, when AgCNPs are suspended.

  16. Rapid, facile synthesis of conjugated polymer zwitterions in ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Page, Zachariah A. [Polymer Science & Engineering Department; Conte Center for Polymer Research; University of Massachusetts; Amherst, USA; Liu, Feng [Polymer Science & Engineering Department; Conte Center for Polymer Research; University of Massachusetts; Amherst, USA; Russell, Thomas P. [Polymer Science & Engineering Department; Conte Center for Polymer Research; University of Massachusetts; Amherst, USA; Emrick, Todd [Polymer Science & Engineering Department; Conte Center for Polymer Research; University of Massachusetts; Amherst, USA

    2014-01-01

    Ionic liquids (ILs) were utilized for the rapid air-stable Suzuki polymerization of polar zwitterionic thiophene monomers, precluding the need for volatile organic solvents, phosphine ligands and phase transfer catalysts typically used in conjugated polymer synthesis.

  17. Speciation and Attenuation of Arsenic and Selenium at Coal Combustion By-Product Management Facilities

    Energy Technology Data Exchange (ETDEWEB)

    K. Ladwig

    2005-12-31

    The overall objective of this project was to evaluate the impact of key constituents captured from power plant air streams (principally arsenic and selenium) on the disposal and utilization of coal combustion products (CCPs). Specific objectives of the project were: (1) to develop a comprehensive database of field leachate concentrations at a wide range of CCP management sites, including speciation of arsenic and selenium, and low-detection limit analyses for mercury; (2) to perform detailed evaluations of the release and attenuation of arsenic species at three CCP sites; and (3) to perform detailed evaluations of the release and attenuation of selenium species at three CCP sites. Each of these objectives was accomplished using a combination of field sampling and laboratory analysis and experimentation. All of the methods used and results obtained are contained in this report. For ease of use, the report is subdivided into three parts. Volume 1 contains methods and results for the field leachate characterization. Volume 2 contains methods and results for arsenic adsorption. Volume 3 contains methods and results for selenium adsorption.

  18. The effects of pf grind quality on coal burnout in a 1 MW combustion test facility

    Energy Technology Data Exchange (ETDEWEB)

    Richelieu Barranco; Michael Colechin; Michael Cloke; Will Gibb; Edward Lester [University of Nottingham, Nottingham (United Kingdom). School of Chemical, Environmental and Mining Engineering, Nottingham Fuel and Energy Centre

    2006-05-15

    A study was carried out to determine the effect of pf particle size distribution on coal burnout propensity in a 1 MW pulverised fuel burner. The specific aim of the work was to assess the improvement in combustion performance achievable by retrofitting commercially available high performance static or dynamic classifiers to existing plants. Two coals were used and were selected as representative of extremes in fuel characteristics experienced by coal importing utilities in Europe. Each coal was fired in the unit at a range of grind sizes to determine the overall impact of a variable performance from a mill. The levels of unburnt carbon in the resultant flyashes for the two coals showed significantly different behaviour. For the higher volatile coal, the unburnt carbon was found to be insensitive to grind quality. However, the coarser grinds of the other coal produced significantly lower unburnt carbon than expected when compared with the finest grinds. Generally the results indicate that the installation of improved classification technology, leading to a finer product, will help to lower unburnt carbon levels. Nevertheless, further work will be necessary to establish the levels of diminishing returns for grind size, burnout performance and grind costs. 21 refs., 4 figs., 4 tabs.

  19. Microwave-assisted combustion synthesis of nano iron oxide/iron-coated activated carbon, anthracite, cellulose fiber, and silica, with arsenic adsorption studies

    Science.gov (United States)

    Combustion synthesis of iron oxide/iron coated carbons such as activated carbon, anthracite, cellulose fiber and silica is described. The reactions were carried out in alumina crucibles using a Panasonic kitchen microwave with inverter technology, and the reaction process was com...

  20. Solution-combustion synthesis of Bi1–xLnxO1⋅ 5 (Ln= Y and La–Yb ...

    Indian Academy of Sciences (India)

    combustion synthesis of Bi1–LnO1.5 (Ln = Y and La–Yb) oxide ion conductors. Manjunath B Bellakki A S Prakash C Shivakumara M S Hegde A K Shukla. Ceramics and Glasses Volume 29 Issue 4 August 2006 pp 339-345 ...

  1. Solution combustion synthesis of (La, K) FeO3 orthoferrite ceramics ...

    Indian Academy of Sciences (India)

    Administrator

    Fourier transform infrared spectroscopy (FTIR), and magnetic and optical property ... Among many perovskite ceramics, LaFeO3 is of cur- ... example, in anode-supported SOFCs, doped LaFeO3 used ... doped with K+, synthesized by a simple combustion ... single phase formation was limited to ... magnetic field of 1000 Oe.

  2. Combustion synthesis of nanocrystalline ceria (CeO2) powders by a dry route

    International Nuclear Information System (INIS)

    Hwang, C.-C.; Huang, T.-H.; Tsai, J.-S.; Lin, C.-S.; Peng, C.-H.

    2006-01-01

    In this study, ceria (CeO 2 ) powders were synthesized with 50 g per batch via a combustion technique using two kinds of starting materials-urea [(NH 2 ) 2 CO] (as a fuel) and ceric ammonium nitrate [Ce(NH 4 ) 2 (NO 3 ) 6 ] (acting as both the source of cerium ion and an oxidizer). The starting materials were mixed thoroughly without adding water, and then ignited in the air at room temperature. It underwent a self-combustion process with a large amount of smoke, a voluminous loose product. The as-synthesized powders were characterized by X-ray diffraction (XRD) analysis, transmission electron microscope (TEM), scanning electron microscope (SEM), CHN elemental analyzer, surface area measurements, and sinterability. Experimental results revealed that the nanocrystalline CeO 2 powders with low impurity content ( 2 /g and ∼25 nm, respectively, through the stoichiometric fuel/oxidizer ratio reaction. The powder, when cold pressed and sintered in the air at 1250 deg. C for 1 h, was measured to attain the sintered density ∼92% of theoretical density having submicron grain size. In addition, the thermal decomposition and combustion process of the reactant mixture were investigated using thermogravimetry (TG), differential scanning calorimetry (DSC), and mass spectrometry (MS) techniques simultaneously. Based on the results of thermal analysis, a possible mechanism concerning the combustion reaction is proposed

  3. SYNTHESIS AND ANALYSIS OF La o.9 MnO 3 BY COMBUSTION ...

    African Journals Online (AJOL)

    The Lao.9MnO3 has been synthesized from lanthanum acetylacetonate, manganese acetylacetonate and urea by combustion method at 800oC. The analysis of the synthesized Lao.9MnO3 show it to be a semi-conducting nanopolycrystalline material having orthorhombic geometry with unit-cell parameters: a = 5.50335Ao; ...

  4. Effect of Fe on the phases and microstructure of TiC-Fe cermets by combustion synthesis/quasi-isostatic pressing

    International Nuclear Information System (INIS)

    Zhang Weifang; Zhang Xinghong; Wang Jianli; Hong Changqing

    2004-01-01

    Fully dense TiC-Fe cermets (x = 10, 20, 30, and 40 wt.%) were produced from Ti-C-Fe powder mixtures by combustion synthesis with quasi-isostatic pressing. The effect of Fe content on combustion temperature, combustion wave velocity, and final product density was investigated. The final product was characterized by XRD, SEM, and TEM. The combustion temperature and wave velocity decreased with increasing Fe content. Product density increased with increasing Fe content (96% at 30 wt.%). X-ray diffraction and transmission electron microscopy (TEM) revealed the final product to contain TiC, Fe phases, lath martensite, and Fe 2 Ti. The TiC particle size decreased with increasing Fe content. In addition, a low density of dislocations was observed in both the TiC particles and Fe binder, indicative of annealing and recrystallization, respectively

  5. Banyan latex: a facile fuel for the multifunctional properties of MgO nanoparticles prepared via auto ignited combustion route

    International Nuclear Information System (INIS)

    Anil Kumar, M R; Nagaswarupa, H P; Gurushantha, K; Pratapkumar, C; Prashantha, S C; Shashishekar, T R; Anantharaju, K S; Nagabhushana, H; Sharma, S C; Vidya, Y S; Daruka Prasad, B; Vivek Babu, C S; Vishnu Mahesh, K R

    2015-01-01

    MgO nanoparticles (MNPs) were prepared by a solution combustion route using banyan tree (BT) latex and glycine as fuels. The powder x-ray diffraction results indicate the formation of a single cubic phase and the crystallite size obtained from transmission electron microscopy was found to be ∼10–15 nm. Scanning electron microscopy result reveals spherical-shaped particles obtained with BT latex. However, in a chemical route, porous and agglomerated particles were obtained. The energy band gap of MNPs obtained using BT latex and a chemical route were found to be in the range 4.85–5.0 eV. Photoluminescence peaks observed at 473, 514, and 588 nm when excited at 433 nm, which were attributed to surface defects. The enhanced photocatalytic activities of spherical MgO were due to smaller crystallite size, higher surface defects, dye sensitization, and capability to reduce the electron–hole pair recombination. Further, green-synthesized MNPs exhibit superior antifungal activity against various plant pathogens. The present studies demonstrated a green engineering route for the synthesis of multifunctional MNPs using BT latex. (paper)

  6. Facile Synthesis of Monodisperse Gold Nanocrystals Using Virola oleifera

    Science.gov (United States)

    Milaneze, Bárbara A.; Oliveira, Jairo P.; Augusto, Ingrid; Keijok, Wanderson J.; Côrrea, Andressa S.; Ferreira, Débora M.; Nunes, Otalíbio C.; Gonçalves, Rita de Cássia R.; Kitagawa, Rodrigo R.; Celante, Vinícius G.; da Silva, André Romero; Pereira, Ana Claudia H.; Endringer, Denise C.; Schuenck, Ricardo P.; Guimarães, Marco C. C.

    2016-10-01

    The development of new routes and strategies for nanotechnology applications that only employ green synthesis has inspired investigators to devise natural systems. Among these systems, the synthesis of gold nanoparticles using plant extracts has been actively developed as an alternative, efficient, cost-effective, and environmentally safe method for producing nanoparticles, and this approach is also suitable for large-scale synthesis. This study reports reproducible and completely natural gold nanocrystals that were synthesized using Virola oleifera extract. V. oleifera resin is rich in epicatechin, ferulic acid, gallic acid, and flavonoids (i.e., quercetin and eriodictyol). These gold nanoparticles play three roles. First, these nanoparticles exhibit remarkable stability based on their zeta potential. Second, these nanoparticles are functionalized with flavonoids, and third, an efficient, economical, and environmentally friendly mechanism can be employed to produce green nanoparticles with organic compounds on the surface. Our model is capable of reducing the resin of V. oleifera, which creates stability and opens a new avenue for biological applications. This method does not require painstaking conditions or hazardous agents and is a rapid, efficient, and green approach for the fabrication of monodisperse gold nanoparticles.

  7. Microstructure and kinetics of a functionally graded NiTi-TiC x composite produced by combustion synthesis

    International Nuclear Information System (INIS)

    Burkes, Douglas E.; Moore, John J.

    2007-01-01

    Production of a NiTi-TiC x functionally graded material (FGM) composite is possible through use of a combustion synthesis (CS) reaction employing the propagating mode (SHS). The NiTi-TiC x FGM combines the well-known and understood superelastic and shape memory capabilities of NiTi with the high hardness, wear and corrosion resistance of TiC x . The material layers were observed as functionally graded both in composition and porosity with distinct interfaces, while still maintaining good material interaction and bonding. XRD of the FGM composite revealed the presence of TiC x with equi-atomic NiTi and minor NiTi 2 and NiTi 3 phases. The TiC x particle size decreased with increasing NiTi content. Microindentation performed across the length of the FGM revealed a decrease in hardness as the NiTi content increased

  8. Development and characterization of Mn{sup 2+}-doped MgO nanoparticles by solution combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Basha, Md. Hussain; Gopal, N. O., E-mail: nogopal@yahoo.com [Department of Physics, Vikrama Simhapuri University Post Graduate Center, Kavali-524201 (India); Rao, J. L. [Department of physics, Sri Venkateswara University, Tirupati-517502 (India); Nagabhushana, H. [Prof. C.N.R. Rao Centre for Nano Research, Tumkur University, Tumkur-572103 (India); Nagabhushana, B. M. [Department of Chemistry, M.S. Ramaiah Institute of Technology, Bangalore - 560054 (India); Chakradhar, R. P. S. [CSIR- National Aerospace Laboratories, Bangalore -560017 (India)

    2015-06-24

    Mn doped MgO Nanoparticles have been prepared by Solution Combustion Synthesis. The synthesized sample is characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Electron Paramagnetic Resonance (EPR). The prepared MgO:Mn (1 mol%) nano crystals appear to be of simple cubic crystalline phase with lattice parameters a = 4.218(2) Å and cell volume = 74.98 (7) Å{sup 3}. SEM micrograph of powders show highly porous, many agglomerates with irregular morphology, large voids, cracks and pores. EPR spectrum of the sample at room temperature exhibit an isotropic sextet hyperfine pattern, centered at g=1.99, characteristic if Mn{sup 2+} ions with S=I=5/2.The observed g value and the hyperfine value reveal the ionic bonding between Mn{sup 2+} and its surroundings.

  9. Facile hydrothermal synthesis of CeO 2 nanopebbles

    Indian Academy of Sciences (India)

    Cerium oxide (CeO2) nanopebbles have been synthesized using a facile hydrothermal method. X-ray diffraction pattern (XRD) and transmission electron microscopy analyses confirm the presence of CeO2 nanopebbles. XRD shows the formation of cubic fluorite CeO2 and the average particle size estimated from the ...

  10. Arylazoindazole Photoswitches : Facile Synthesis and Functionalization via SNAr Substitution

    NARCIS (Netherlands)

    Travieso-Puente, Raquel; Budzak, Simon; Chen, Juan; Stacko, Peter; Jastrzebski, Johann T B H; Jacquemin, Denis; Otten, Edwin

    2017-01-01

    A straightforward synthetic route to arylazoindazoles via nucleophilic aromatic substitution is presented. Upon deprotonation of the NH group, a C6F5-substituted formazan undergoes facile cyclization as a result of intermolecular nucleophilic substitution (SNAr). This new class of azo photoswitches

  11. Facile, eco-friendly, catalyst-free synthesis of polyfunctionalized quinoxalines.

    Science.gov (United States)

    Zhang, Yaohong; Luo, Mengqiang; Li, Yan; Wang, Hai; Ren, Xiaorong; Qi, Chenze

    2018-02-01

    A novel, facile and eco-friendly synthesis of quinoxalines from [Formula: see text] and 1,2-diamines was developed. An attractive feature of this protocol is that the desired products could be generated efficiently in water and without any catalyst, which is in accordance with the aim of green chemistry. A plausible mechanism has been proposed.

  12. Comparative analysis of synthesis and characterization of La_0_,_9Sr_0_,_1O_3 via sol-gel and combustion reaction

    International Nuclear Information System (INIS)

    Tarrago, D.P.; Haeser, G.S.; Malfatti, C.F.; Sousa, V.C.

    2011-01-01

    Strontium doped lanthanum manganites (LSM) are potential materials for cathode application in solid oxide fuel cells (SOFC) due to their properties and compatibility with yttria stabilized zirconia. In this work a LSM powder obtained by the sol-gel process is compared others previously obtained combustion synthesis using urea or sucrose as fuel. For the synthesis of LSM the nitrates of lanthanum, strontium and manganese were dissolved in citric acid and ethylene glycol forming a gel that was calcinated at 800 deg C. Both methods allowed the synthesis of a single phase powder, according to the X-ray diffraction patterns. Through gas adsorption it was found a specific surface area of 17m²/g, an intermediary value among the combustion synthesized powders. Scanning electron microscopy (SEM) revealed more compact agglomerates in the sol-gel powder, however, the transmission electron microscope (TEM) showed smaller and more uniform particles in this powder. (author)

  13. One step facile synthesis of ferromagnetic magnetite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Suppiah, Durga Devi; Abd Hamid, Sharifah Bee, E-mail: sharifahbee@um.edu.my

    2016-09-15

    The ferromagnetic properties of magnetite (Fe{sub 3}O{sub 4}) were influenced by the nanoparticle size, hence importance were given to the synthesis method. This paper clearly shows that magnetite nanoparticles were successfully synthesized by employing one step controlled precipitation method using a single salt (Iron(II) sulfate) iron precursor. The acquired titration curve from this method provides vital information on the possible reaction mechanism leading to the magnetite (Fe{sub 3}O{sub 4}) nanoparticles formation. Goethite (α-FeOOH) was obtained at pH 4, while the continuous addition of hydroxyl ions (OH{sup −}) forms iron hydroxides (Fe(OH){sub 2}). This subsequently reacts with the goethite, producing magnetite (Fe{sub 3}O{sub 4}) at pH 10. Spectroscopy studies validate the magnetite phase existence while structural and morphology analysis illustrates cubic shaped magnetite with an average size of 35 nm was obtained. The synthesized magnetite might be superparamagnetic though lower saturation magnetization (67.5 emu/g) measured at room temperature as compared to bulk magnetite. However the nanoparticles surface anisotropy leads to higher remanence (12 emu/g) and coercivity (117.7 G) making the synthesized magnetite an excellent candidate to be utilized in recording devices. The understanding of the magnetite synthesis mechanism can not only be used to achieve even smaller magnetite nanoparticles but also to prepare different types of iron oxides hydroxides using different iron precursor source. - Highlights: • Magnetite strong magnetism properties make it versatile in various applications including biomedical and electromagnetic materials. • Sulfate (SO{sub 4}{sup 2−}) anion plays a major role in the structure control of iron oxide during synthesis. • Phase pure magnetite nanoparticles with high magnetism properties can be obtained using a single salt (SO{sub 4}{sup 2−}) method.

  14. Synthesis of antimony-doped tin oxide (ATO) nanoparticles by the nitrate-citrate combustion method

    International Nuclear Information System (INIS)

    Zhang Jianrong; Gao Lian

    2004-01-01

    Antimony-doped tin oxide (ATO) nanoparticles having rutile structure have been synthesized by the combustion method using citric acid (CA) as fuel and nitrate as an oxidant, the metal sources were granulated tin and Sb 2 O 3 . The influence of citric acid (fuel) to metal ratio on the average crystallite size, specific surface area and morphology of the nanoparticles has been investigated. X-ray diffraction showed the tin ions were reduced to elemental tin during combustion reaction. The average ATO crystallite size increased with the increase of citric acid (fuel). Powder morphology and the comparison of crystallite size and grain size shows that the degree of agglomeration of the powder decreased with an increase of the ratio. The highest specific surface area was 37.5 m 2 /g when the citric acid to tin ratio was about 6

  15. FACILE SYNTHESIS OF 1-NAPHTHOL AZO DYES WITH NANO ...

    African Journals Online (AJOL)

    Preferred Customer

    a highly efficient and one pot synthesis of azo dyes based on 1-naphthol under ... known and were identified by comparison of their physical and spectroscopic data with those of ... δ: 16.15 (s, 1H), 8.41 (d, J = 7.6 Hz, 1 H), 8.33 (d, J = 8.8 Hz, 2H), 7.8 (d, .... 86. 81. 77. 70. 65. N2. + IO4. -. O2N. 2d. 96. 93. 90. 85. 79. 73. 69.

  16. Facile synthesis of Ag nanocubes and Au nanocages.

    Science.gov (United States)

    Skrabalak, Sara E; Au, Leslie; Li, Xingde; Xia, Younan

    2007-01-01

    This protocol describes a method for the synthesis of Ag nanocubes and their subsequent conversion into Au nanocages via the galvanic replacement reaction. The Ag nanocubes are prepared by a rapid (reaction time nanocubes. With this method, Ag nanocubes can be prepared and isolated for use within approximately 3 h. The Ag nanocubes can then serve as sacrificial templates for the preparation of Au nanocages, with a method for their preparation also described herein. The procedure for Au nanocage preparation and isolation requires approximately 5 h.

  17. Synthesis and characterization of a ferrous compound material obtained by combustion of ferroboron and ferrotitanium mixtures

    International Nuclear Information System (INIS)

    Bejar, M.A; Fuenzalida, J.L

    2008-01-01

    A ferrous compound material was synthesized in this work, by the air auto-combustion of mixtures of powdered ferroboron and ferrotitanium, compacted under pressures of 79 and 93 MPa and preheated to a temperature of about 1000 o C. The synthesized compounds were characterized by XRD analysis, and macro and micro-hardness tests. The formation of titanium diboride was found in all the synthesized test pieces (au)

  18. Influence of fuel ratios on auto combustion synthesis of barium ferrite

    Indian Academy of Sciences (India)

    Abstract. Single-domain barium ferrite nano particles have been synthesized with narrow particle-size distribution using an auto combustion technique. In this process, citric acid was used as a fuel. Ratios of cation to fuel were maintained variously at 1 : 1, 1 : 2 and 1 : 3. The pH was 7 in all cases. Of all three cases, a cation ...

  19. In situ synthesis and formation mechanism of ZrC and ZrB2 by combustion synthesis from the Co-Zr-B4C system

    Directory of Open Access Journals (Sweden)

    Mengxian Zhang

    2015-09-01

    Full Text Available ZrC-ZrB2-based composites were prepared by combustion synthesis (CS reaction from 10 wt.% to 50 wt.% Co-Zr-B4C powder mixtures. With increasing Co contents, the particle sizes of near-spherical ZrC and platelet-like ZrB2 decreased from 1 μm to 0.5 μm and from 5 μm to 2 μm, respectively. In addition, the formation mechanism of ZrC and ZrB2 was explored by the phase transition and microstructure evolution on the combustion wave quenched sample in combination with differential scanning calorimeter analysis. The results showed that the production of ZrC was ascribed to the solid-solid reaction between Zr and C and the precipitation from the Co-Zr-B-C melt, while ZrB2 was prepared from the saturated liquid. The low B concentration in the Co-Zr-B-C liquid and high cooling rate during the CS process led to the presence of Co2B and ZrCo3B2 in the composites. The addition of Co in the Co-Zr-B4C system not only prevented ZrC and ZrB2 particulates from growing, but also promoted the occurrence of ZrC-ZrB2-forming reaction.

  20. Self-combustion synthesis and oxygen storage properties of mesoporous gadolinia-doped ceria nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Yang Tao [College of Environmental and Energy Engineering, Beijing University of Technology (BUT-CEEE), Chaoyang District 100124, Beijing (China); Xia Dingguo, E-mail: yangtaophoenix@yahoo.com.cn [College of Environmental and Energy Engineering, Beijing University of Technology (BUT-CEEE), Chaoyang District 100124, Beijing (China)

    2010-10-01

    Ethyl glycol and citric acid, along with metal nitrates have been used to prepare Ce{sub 0.9}Gd{sub 0.1}O{sub 2-x} nanotubes directed at the anodic alumina oxide (AAO) template by combustion route. The tubes produced by the self-combustion route do not need any further calcination step. XRD patterns show the doped-ceria tubes have the flurite-type structure and no impurities are detected. The specific surface area of the tube is 112.7 m{sup 2} g{sup -1} and N{sub 2} adsorption-desorption profiles of the BET measurement shows the tubes are mesoporous. The largest aspect ratio of a nanotube reaches 20:1 and the TEM observation reveals the hollow structure. The Ce:Gd molar ratio calculated from the EDS and ICP-AES is 9:1 and the selected area electron diffraction confirms the flurite-type structure from the XRD characterization. The combined thermogravimetry-differential thermal analysis has been carried out to study the combustion reactions in the tube-forming process. The thermal stability of the nanotubes under both reductive and oxidative atmospheres is tested using the dynamic reduction/reoxidation reactions. At last, the oxygen storage capacity (OSC) of the nanotubes is calculated to be 695 {mu}mol-O{sup 2} g{sup -1} from the temperature-programed reduction reaction.

  1. Sol-gel auto-combustion synthesis of hydroxyapatite nanotubes array in porous alumina template

    International Nuclear Information System (INIS)

    Yuan Yuan; Liu Changsheng; Zhang Yuan; Shan Xiaoqian

    2008-01-01

    In this paper, an array of highly ordered hydroxyapatite (HAP) nanotubes was synthesized by sol-gel auto-combustion method with porous anodic aluminum oxide (AAO) template for the first time. Based on thermogravimetry (DTA/TG), Fourier transform infrared (FTIR) and X-ray diffraction (XRD), the dried gel, derived from the sol solution with Ca(NO 3 ) 2 .4H 2 O and PO(CH 3 O) 3 as precursors and ethylene glycol as the polymeric matrix, exhibited a typical self-propagating combustion behavior at low temperature, directly resulting in hexagonal crystalline HAP materials. The resultant HAP arrays fabricated from the above sol-gel in the AAO template were uniformly distributed, highly ordered nanotubes with uniform length and diameter according to the observations of scanning electron microscopy (SEM) and transmission electron microscope (TEM). The electron diffraction (ED), XRD and X-ray photoelectron spectroscopy (XPS) survey proved the formation of HAP phase with polycrystalline structure in the AAO template. Based on these results, a potential mechanism of 'an auto-combustion from dried gel to nanoparticles and a subsequent in situ reaction from nanoparticles to nanotubes' was proposed

  2. 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.

  3. 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.

  4. A Facile Synthesis of Dynamic, Shape Changing Polymer Particles

    OpenAIRE

    Klinger, Daniel; Wang, Cynthia; Connal, Luke A.; Audus, Debra J.; Jang, Se Gyu; Kraemer, Stephan; Killops, Kato L.; Fredrickson, Glenn H.; Kramer, Edward J.; Hawker, Craig J.

    2014-01-01

    We herein report a new facile strategy to ellipsoidal block copolymer nanoparticles exhibiting a pH-triggered anistropic swelling profile. In a first step, elongated particles with an axially stacked lamellae structure are selectively prepared by utilizing functional surfactants to control the phase separation of symmetric PS-b-P2VP in dispersed droplets. In a second step, the dynamic shape change is realized by crosslinking the P2VP domains, hereby connecting glassy PS discs with pH-sensitiv...

  5. Antitubercular activity of ZnO nanoparticles prepared by solution combustion synthesis using lemon juice as bio-fuel.

    Science.gov (United States)

    Gopala Krishna, Prashanth; Paduvarahalli Ananthaswamy, Prashanth; Trivedi, Priyanka; Chaturvedi, Vinita; Bhangi Mutta, Nagabhushana; Sannaiah, Ananda; Erra, Amani; Yadavalli, Tejabhiram

    2017-06-01

    In this study, we report the synthesis, structural and morphological characteristics of zinc oxide (ZnO) nanoparticles using solution combustion synthesis method where lemon juice was used as the fuel. In vitro anti-tubercular activity of the synthesized ZnO nanoparticles and their biocompatibility studies, both in vitro and in vivo were carried out. The synthesized nanoparticles showed inhibition of Mycobacterium tuberculosis H37Ra strain at concentrations as low as 12.5μg/mL. In vitro cytotoxicity study performed with normal mammalian cells (L929, 3T3-L1) showed that ZnO nanoparticles are non-toxic with a Selectivity Index (SI) >10. Cytotoxicity performed on two human cancer cell lines DU-145 and Calu-6 indicated the anti-cancer activity of ZnO nanoparticles at varied concentrations. Results of blood hemolysis indicated the biocompatibility of ZnO nanoparticles. Furthermore, in vivo toxicity studies of ZnO nanoparticles conducted on Swiss albino mice (for 14days as per the OECD 423 guidelines) showed no evident toxicity. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides

    Directory of Open Access Journals (Sweden)

    Mao-Sheng Cheng

    2008-07-01

    Full Text Available Oleanolic acid and its glycosides are important natural products, possessing various attractive biological activities such as antitumor, antivirus and anti-inflammatory properties. In the present work, fifteen oleanolic acid saponins bearing various saccharide moieties, including 3-monoglycoside, 28-monoglycoside and 3,28-diglycoside, were easily synthesized in high yields. Benzyl was chosen as the protective group for the COOH(28 group, instead of commonly used methyl and allyl, to avoid difficulties in the final deprotection. Alkali-promoted condensation of the carboxylic acid with bromoglycosides was found to be more efficient in the synthesis of 28-glycosides. Two approaches were investigated and proved practicable in the preparation of 3,28- diglycosides. This method is suitable for preparing oleanolic acid glycosides with structural diversity for extensive biological evaluation and structure-activity relationship study, and it also apply new idea for the corresponding synthetic methods to the glycoside derivatives of other triterpenoid.

  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. Facile synthesis of gold nanomaterials with unusual crystal structures.

    Science.gov (United States)

    Fan, Zhanxi; Huang, Xiao; Chen, Ye; Huang, Wei; Zhang, Hua

    2017-11-01

    Gold (Au) nanomaterials have attracted wide research attention, owing to their high chemical stability, promising catalytic properties, excellent biocompatibility, unique electronic structure and outstanding localized surface plasmon resonance (LSPR) absorption properties; all of which are closely related to their size and shape. Recently, crystal-phase-controlled synthesis of noble metal nanomaterials has emerged as a promising strategy to tune their physicochemical properties. This protocol describes the detailed experimental procedures for the crystal-phase-controlled syntheses of Au nanomaterials with unusual crystal structures under mild conditions. Briefly, pure hexagonal close-packed (hcp) Au square sheets (AuSSs) with a thickness of ∼2.4 nm are synthesized using a graphene-oxide-assisted method in which HAuCl 4 is reduced by oleylamine in a mixture of hexane and ethanol. By using pure hexane as the solvent, well-dispersed ultrathin hcp/face-centered cubic (fcc) Au nanowires with a diameter of ∼1.6 nm on graphene oxide can be obtained. Meanwhile, hcp/fcc Au square-like plates with a side length of 200-400 nm are prepared via the secondary growth of Au on the hcp AuSSs. Remarkably, hexagonal (4H) Au nanoribbons with a thickness of 2.0-6.0 nm can be synthesized with a one-pot colloidal method in which HAuCl 4 is reduced by oleylamine in a mixed solvent of hexane and 1,2-dichloropropane. It takes 17-37 h for the synthesis of these Au nanomaterials with unusual crystal structures. Transmission electron microscopy (TEM) and atomic force microscopy (AFM) are used to characterize the resultant Au nanomaterials, which could have many promising applications, such as biosensing, near-IR photothermal therapy, catalysis and surface-enhanced Raman scattering (SERS).

  9. Facile combustion synthesis of novel CaZrO3:Eu , Gd red phosphor ...

    Indian Academy of Sciences (India)

    When the Gd3+ ions were introduced in this compound, the emissions of ... a doped nanostructure may suppress resonant energy trans- ... light.17,18 In this paper, we report a fast and efficient pro- cedure for .... stages of weight loss at temperatures between 258 and 600 ... or particle size as the dopant ions are introduced.

  10. A Facile Synthesis of Dynamic, Shape Changing Polymer Particles

    Science.gov (United States)

    Klinger, Daniel; Wang, Cynthia; Connal, Luke A.; Audus, Debra J.; Jang, Se Gyu; Kraemer, Stephan; Killops, Kato L.; Fredrickson, Glenn H.; Kramer, Edward J.; Hawker, Craig J.

    2014-01-01

    We herein report a new facile strategy to ellipsoidal block copolymer nanoparticles exhibiting a pH-triggered anistropic swelling profile. In a first step, elongated particles with an axially stacked lamellae structure are selectively prepared by utilizing functional surfactants to control the phase separation of symmetric PS-b-P2VP in dispersed droplets. In a second step, the dynamic shape change is realized by crosslinking the P2VP domains, hereby connecting glassy PS discs with pH-sensitive hydrogel actuators. PMID:24700705

  11. A facile synthesis of dynamic, shape-changing polymer particles.

    Science.gov (United States)

    Klinger, Daniel; Wang, Cynthia X; Connal, Luke A; Audus, Debra J; Jang, Se Gyu; Kraemer, Stephan; Killops, Kato L; Fredrickson, Glenn H; Kramer, Edward J; Hawker, Craig J

    2014-07-01

    We herein report a new facile strategy to ellipsoidal block copolymer nanoparticles that exhibit a pH-triggered anistropic swelling profile. In a first step, elongated particles with an axially stacked lamellae structure are selectively prepared by utilizing functional surfactants to control the phase separation of symmetric polystyrene-b-poly(2-vinylpyridine) (PS-b-P2VP) in dispersed droplets. In a second step, the dynamic shape change is realized by cross-linking the P2VP domains, thereby connecting glassy PS discs with pH-sensitive hydrogel actuators. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Bulk synthesis of nanocrystalline urania powders by citrate gel-combustion method

    International Nuclear Information System (INIS)

    Sanjay Kumar, D.; Ananthasivan, K.; Venkata Krishnan, R.; Amirthapandian, S.; Dasgupta, Arup

    2016-01-01

    Bulk quantities (60 g) of nanocrystalline (nc) free flowing urania powders with crystallite size ranging from 38 to 252 nm have been synthesized for the first time by the citrate gel combustion method. A systematic study of the influence of the fuel (citric acid) to oxidant (nitrate) ratio (R) on the characteristics of the urania powders has been carried out for the first time. Mixture with an “R” value of 0.25 exhibited a vigorous auto-ignition reaction. This reaction was investigated with Differential Scanning Calorimetry (DSC) and in-situ thermogravimetry coupled with differential thermal analysis and mass spectrometry (TG-DTA-MS). The bulk density, specific surface area, X-ray crystallite size, residual carbon and size distribution of particles of this powder were unique. Microscopic and microstructural investigation of selected samples revealed the presence of nanocrystals with irregular exfoliated morphology; their Electron Energy Loss Spectra testified the covalency of the U–O bond. - Highlights: • Bulk quantities of nanocrystalline urania were prepared for the first time using citrate gel combustion method. • Volume combustion was observed in mixtures with fuel to nitrate ratio (R) 0.25. • The value of R was found to significantly influence the characteristics of the final product. • Typical exfoliated microstructure and nanopores were observed. • Established correlation between particle size distribution and bulk density, X-ray crystallite size and lattice strain. • Relationship between fuel to nitrate (R) mole ratio and physical characteristics of powders were also established.

  13. Synthesis, characterization of nickel aluminate nanoparticles by microwave combustion method and their catalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Ragupathi, C. [Catalysis and Nanomaterials Research Laboratory, Department of Chemistry, Loyola College (Autonomous), Chennai 600034 (India); Vijaya, J. Judith, E-mail: jjvijayaloyola@yahoo.co.in [Catalysis and Nanomaterials Research Laboratory, Department of Chemistry, Loyola College (Autonomous), Chennai 600034 (India); Kennedy, L. John [Materials Division, School of Advanced Sciences, Vellore Institute of Technology (VIT) University, Chennai Campus, Chennai 600127 (India)

    2014-05-01

    Highlights: • Simple route for the preparation of nickel aluminate. • NiAl{sub 2}O{sub 4} microwave absorbent was invented by a simple method. • High specific surface area was obtained at low temperature. • Evaluation of magnetic, optical and catalytic properties. - Abstract: Microwave combustion method (MCM) is a direct method to synthesize NiAl{sub 2}O{sub 4} nanoparticles and for the first time we report the using of Sesame (Sesame indicum L.) plant extract in the present study. Solutions of metal nitrates and plant extract as a gelling agent are subsequently combusted using microwave. The structure and morphology of NiAl{sub 2}O{sub 4} nanoparticles are investigated by X-ray diffraction (XRD), Fourier transforms infrared spectra (FT-IR), high resolution scanning electron microscopy (HR-SEM), energy dispersive X-ray analysis (EDX), high resolution transmission electron microscopy (HR-TEM), diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) spectroscopy, Brunauer–Emmett–Teller (BET) analysis and vibrating sample magnetometer (VSM). XRD pattern confirmed the formation of cubic phase NiAl{sub 2}O{sub 4}. The formation of NiAl{sub 2}O{sub 4} is also confirmed by FT-IR. The formation of NiAl{sub 2}O{sub 4} nanoparticles is confirmed by HR-SEM and HR-TEM. Furthermore, the microwave combustion leads to the formation of fine particles with uniform morphology. The magnetic properties of the synthesized NiAl{sub 2}O{sub 4} nano and microstructures were investigated by vibrating sample magnetometer (VSM) and their hysteresis loops were obtained at room temperature. Further, NiAl{sub 2}O{sub 4} prepared by MCM using Sesame (S. indicum L.) plant extract is tested for the catalytic activity toward the oxidation of benzyl alcohol.

  14. Solution-combustion synthesis of Tb3+-doped Y3Al5O12 nanoparticles

    International Nuclear Information System (INIS)

    Fadlalla, H.M.H.; Tang, C.C.; Elsanousi, A.; Ding, X.X.; Qi, S.R.

    2009-01-01

    Nano-sized YAG:Tb powder phosphors were prepared by a solution-combustion method, using the general inorganic salts as starting materials. The X-ray diffraction (XRD) measurements showed that the precursor can be well-crystallized at 900 deg. C. As-prepared particles have sizes mostly in the range between 30 and 100 nm as obtained by scanning electron microscope (SEM) and transition electron microscope (TEM). Selected area electron diffraction (SAED) patterns proved that the larger particles are monocrystalline. The effects of annealing temperature and Tb-doping concentration on the luminescence intensity were studied

  15. Combustion synthesis and catalytic activity of LaCoO{sub 3} for HMX thermal decomposition

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Zhi-Xian; Chi, Ying-Nan [Department of Chemistry, Institute for Chemical Physics, Beijing Institute of Technology (China); Hu, Chang-Wen [State Key Laboratory of Explosion Science, Technology Beijing Institute of Technology, Beijing (China); Liu, Hai-Yan [Department of Chemistry, Science Institute, North China University, Taiyuan, Shanxi (China)

    2009-10-15

    Perovskite-type LaCoO{sub 3} was prepared by stearic acid solution combustion method and characterized by XRD, DSC-TG, and XPS techniques. The catalytic activities of LaCoO{sub 3} for HMX (octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine) thermal decomposition were investigated. The as-prepared LaCoO{sub 3} shows higher activity than the calcined one. This could be due to higher concentration of surface-adsorbed oxygen and hydroxyl species as well as higher BET surface area of the as-prepared LaCoO{sub 3}. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  16. Synthesis of micro- and nanodiamonds by the method of oxy- acetylene combustion flame

    International Nuclear Information System (INIS)

    Sabitov, S; Medyanova, B; Partizan, G; Koshanova, A; Mansurova, M; Lesbayev, B; Mansurov, B; Merkibayev, Ye

    2016-01-01

    This work presents the results of experiments on synthesis of micro- and nanodiamonds by the method of oxy-acetylene torch on the surface of pre-deposited copper thin films. The influence of the thickness of the buffer copper film and the concentration ratio of oxygen and acetylene on the structure formation of the deposited samples was investigated during performed experiments. Studies by Raman scattering and scanning electron microscopy showed that the synthesis of micro- and nano-diamonds occurs under certain experimental conditions. (paper)

  17. Solution combustion synthesis of the nanocrystalline NCM oxide for lithium-ion battery uses

    Science.gov (United States)

    Habibi, Amirhosein; Jalaly, Maisam; Rahmanifard, Roohollah; Ghorbanzadeh, Milad

    2018-02-01

    In this study, the NCM cathode with a chemical composition of {{{LiNi}}}1/3}{{{Co}}}1/3}{{{Mn}}}1/3}{{{O}}}2 were synthesized through a solution combustion method. In this method, metal nitrates and urea were used as precursors and fuel, respectively. The powder obtained from combustion were transferred into a alumina crucible and insert to the muffle furnace and calcined at 750 °C for 15 h. The crystallite size of the sample was calculated with sherer equation to be about 41 nm. The prepared cathode were characterized using x-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetry analysis (TGA), differential scanning calorimetry (DSC) and battery charge-discharge test. The initial charge and discharge capacities of {{{LiNi}}}1/3}{{{Co}}}1/3}{{{Mn}}}1/3}{{{O}}}2 electrode containing 94% active material at a rate of 0.05 C in voltage window of 2.5-4.3 V at room temperature was obtained 168.03 and 150.01 mAh g-1, respectively.

  18. Solution combustion synthesis of calcium phosphate particles for controlled release of bovine serum albumin

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Junfeng, E-mail: daidai02304@163.com [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Jiangsu Laboratory of Advanced Functional Materials, Changshu Institute of Technology, Changshu (China); Zhao, Junjie; Qian, Yu; Zhang, Xiali; Zhou, Feifei; Zhang, Hong [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Lu, Hongbin [National Laboratory of Solid State Microstructures, College of Engineering and Applied Sciences, Nanjing University, Nanjing (China); Chen, JianHua; Wang, XuHong [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Jiangsu Laboratory of Advanced Functional Materials, Changshu Institute of Technology, Changshu (China); Yu, Wencong [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China)

    2015-05-01

    Four different phase compositions of calcium phosphate (CaP) particles were prepared via a solution combustion method. X-ray diffraction (XRD) and Rietveld analysis results revealed that the variations in the nominal Ca/P (molar) ratios were found to provide a favorable control in the different proportions of CaP materials. Bovine serum albumin (BSA) was used as a model protein to study the loading and release behavior. The release profile indicated that the BSA release rates depended on the phase compositions of the CaP particles, and showed an order of TCP-BSA > BCP-1-BSA > BCP-2-BSA > HA-BSA. The results suggested that the BSA protein release rate can be controlled by varying the phase compositions of CaP carriers. Moreover, the release process involved two stages: firstly surface diffusion via ion exchange and secondly intraparticle diffusion. - Highlights: • Solution combustion method was an efficient way to produced CaP powders. • Ca/P (molar) ratios provided a favorable control in the different proportions of phase composition. • BSA release rate varied depending on the phase composition of the CaP particles. • Two kinetic models were chosen to simulate the release kinetics of the drugs from CaP carriers.

  19. Combustion synthesis of micron-sized Sm2Co17 particles via mechanochemical processing

    International Nuclear Information System (INIS)

    Liu, W.; McCormick, P.G.

    1998-01-01

    Full text: The spontaneous formation of Sm 2 Co 17 micron-sized particles via a mechanically induced combustion reaction has been investigated. Sm 2 Co 17 alloy particles of 0.1--2 μm in size embedded in a CaO matrix formed directly via a combustion reaction induced by milling the powder mixture of Sm 2 O 3 , CoO, CaO and Ca over a critical time. The micron-sized Sm 2 Co 17 particles were found to have the TbCu 7 -type structure and characterized by a coercivity value of 7.8 kOe while embedded in the CaO matrix. The effect of subsequent heat treatment on the structure and magnetic properties of as-milled samples was also investigated. Removal of the CaO by a carefully controlled washing process yielded micron-sized Sm 2 Co 17 particles without significant oxidation of the particles. These fine Sm 2 Co 17 particles can be used to produce anisotropic bulk or bonded magnets

  20. Facile synthesis of carbon dots with superior sensing ability

    Science.gov (United States)

    Jin, Lin; Li, Jingguo; Liu, Liyun; Wang, Zhenling; Zhang, Xingcai

    2018-04-01

    Carbon dots (CDs) have various applications in biomedical and environmental field, such as bio-imaging, bio-sensing and heavy metal detection. In this study, a novel class of CDs were synthesized using a one-step hydrothermal method. The fabricated CDs displayed stable photoluminescence, good water solubility, and photo stability. Moreover, the functional groups (carboxylic acid moieties and hydroxyls) on the surface of the obtained CDs enable it with superior sensing ability (e.g., very low detectable concentration for Pb2+: 5 nmol/L). With superior detection sensitivity, excellent fluorescent properties and facile fabrication method, the as-obtained CDs can find practical applications as cost-effective and sensitive chemo-sensors in water and food safety field.

  1. Facile synthesis of organically capped PbS nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Nejo, Ayorinde O.; Nejo, Adeola A.; Pullabhotla, Rajasekhar V.S.R. [Department of Chemistry, University of Zululand, Private Bag X1001, Kwadlangezwa (South Africa); Revaprasadu, Neerish, E-mail: nrevapra@pan.uzulu.ac.za [Department of Chemistry, University of Zululand, Private Bag X1001, Kwadlangezwa (South Africa)

    2012-10-05

    Highlights: Black-Right-Pointing-Pointer Hexadecylamine and tri-n-octylphosphine oxide capped PbS nanoparticles have been synthesized. Black-Right-Pointing-Pointer By varying the reaction conditions various morphologies were formed. Black-Right-Pointing-Pointer The formation of the anisotropic particles is due to different growth mechanisms. - Abstract: PbS nanocubes and nanorods were successfully synthesized through a facile route using hexadecylamine (HDA) and tri-n-octylphosphine oxide (TOPO) as surfactants. The structure and morphology of the as-prepared PbS nanocrystals were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution TEM. The morphology of the PbS was influenced by the variation in lead source and organic surfactant. Particles in the shape of spheres, perfect cubes and rods were obtained by variation in reaction conditions. A possible growth mechanism to explain the formation of these PbS nanocubes and nanorods is also discussed.

  2. Facile synthesis and application of a carbon foam with large mesopores

    KAUST Repository

    Fu, Liling

    2013-01-01

    By combining elements of hard- and soft-templating, a facile synthesis method for carbon foams with large mesopores has been demonstrated. A commercial Pluronic surfactant was used as the structure-directing agent as well as the carbon precursor. No micelle swelling agent or post treatment is necessary to enlarge mesopores. As such this method requires fewer synthesis steps and is highly scalable. The as-synthesized meso-carbons showed potential applications in the fields of carbon oxide capture and lithium-sulfur batteries. © 2013 the Owner Societies.

  3. Sandia Combustion Research: Technical review

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-07-01

    This report contains reports from research programs conducted at the Sandia Combustion Research Facility. Research is presented under the following topics: laser based diagnostics; combustion chemistry; reacting flow; combustion in engines and commercial burners; coal combustion; and industrial processing. Individual projects were processed separately for entry onto the DOE databases.

  4. Facile one-pot transformation using structure-guided combustion waves of micro-nanostructured β-Bi2O3 to α-Bi2O3@C and analysis of electrochemical capacitance

    Science.gov (United States)

    Hwang, Hayoung; Shin, Jung-ho; Lee, Kang Yeol; Choi, Wonjoon

    2018-01-01

    Precise phase-transformation can facilitate control of the properties of various materials, while an organic coating surrounding inorganic materials can yield useful characteristics. Herein, we demonstrate facile, selective manipulation of micro-nanostructured bismuth oxide (Bi2O3) for phase transformation from microflower-like β-Bi2O3 to micropill-like α-Bi2O3, with carbon-coating layer deposition, using structure-guided combustion waves (SGCWs). Microflower-like β-Bi2O3 are synthesized as core materials and nitrocellulose is coated on their surfaces for the formation of core-shell hybrid structures of Bi2O3 and chemical fuel. The SGCWs, which propagate along the core-material and fuel interfaces, apply high thermal energy (550-600 °C) and deposit incompletely combusted carbonaceous fuel on the microflower-like β-Bi2O3 to enable transformation to α-phase and carbon-coating-layer synthesis. SGCW-induced improvements to the electrochemical characteristics of the developed micropill-like α-Bi2O3@C, compared with the microflower-like β-Bi2O3, are investigated. The enhanced stability from the α-phase Bi2O3 and micropill-like structures during charge-discharge cycling improves the specific capacitance, while the carbon-coating layers facilitate increased electrical conductivity. SGCW-based methods exhibit high potential for selective phase manipulation and synthesis of carbon coatings surrounding micro-nanomaterials. They constitute a low-cost, fast, large-scale process for metal oxides, ceramics, and hybrid materials, implemented through control of the processing parameters by tuning the temperature, chemical fuel, and ambient conditions.

  5. Facile solvothermal synthesis of graphene-MnOOH nanocomposites

    International Nuclear Information System (INIS)

    Chen Sheng; Zhu Junwu; Huang Huajie; Zeng Guiyu; Nie Fude; Wang Xin

    2010-01-01

    In this paper, we report a facile solvothermal route capable of aligning MnOOH nanocrystals on graphene. X-ray diffraction (XRD) and transmission electron microscopy (TEM) observations indicate that the exfoliated graphene sheets are decorated randomly by MnOOH nanocrystals, forming well-dispersed graphene-MnOOH nanocomposites. Dissolution-crystallization and oriented attachment are speculated to be the vital mechanisms in the synthetic process. The attachment of additives, such as MnOOH nanoparticles, are found to be beneficial for the exfoliation of GO as well as preventing the restack of graphene sheets. Moreover, cyclic voltammetry (CV) analyses suggest that the electrochemical reversibility is improved by anchoring MnOOH on graphene. Notably, the as-fabricated nanocomposites reveal unusual catalytic performance for the thermal decomposition of ammonium perchlorate (AP) due to the concerted effects of graphene and MnOOH. This template-free method is easy to reproduce, and the process proceeds at a low temperature and can be readily extended to prepare other graphene-based nanocomposites. - Graphical abstract: Manganese oxyhydroxide nanocrystals have been successfully attached onto the graphene sheets via an oriented attachment and dissolution-crystallization process, forming a nanocomposite with unusual catalytic capabilities. Display Omitted

  6. Facile synthesis and structure characterization of hexagonal tungsten bronzes crystals

    Science.gov (United States)

    Lee, Jiann-Shing; Liu, Hao-Chuan; Peng, Gao-De; Tseng, Yawteng

    2017-05-01

    A facile molten-salt route was used to synthesize hexagonal Cs0.33WO3, Rb0.33WO3 and K0.30WO3 crystals. The three isostructural compounds were successfully prepared from the reaction of MxWO3 powders (M = Cs, Rb, K) in the CsCl/NaCl, RbCl/NaCl and KCl/NaCl fluxes, respectively. The structure determination and refinement, based on single-crystal X-ray diffraction data, are in agreement with previous works, possessing space group P63/mcm. The a and c parameters vary non-linearly with increasing radii of the M+ cations (rM) that is coordinated to twelve oxygen atoms. Both the volumes of unit-cell and WO6 octahedra vary linearly with rM, which become smaller from Cs0.33WO3 to K0.30WO3. The distortion of WO6 octahedra as well as isotropic displacement parameters increases from Cs0.33WO3 to K0.30WO3. The geometry of the WO6 octahedron becomes more regular with increasing rM. These structural trends arise from the effective size of the M+ cation.

  7. Synthesis of the lithium metatitanate, Li2TiO3, by the modified combustion method

    International Nuclear Information System (INIS)

    Cruz, D.; Bulbulian, S.; Pfeiffer, H.

    2005-01-01

    A modified combustion method to obtain Li 2 TiO 3 it was used, a compound to be used in fusion reactors like tritium generator material. To obtain Li 2 TiO 3 were proven different molar ratios of lithium hydroxide (LiOH), titanium oxide (TiO 2 ) and urea (CO(NH 2 ) 2 ), as well as different heating temperatures (550, 650 and 750 C). The characterization of the products it was carried out using X-ray diffraction, Scanning electron microscopy and Thermal gravimetric analysis. The sample prepared with a molar ratio Li: Ti: urea = 2.75: 1: 3 was the one that presented as only product the Li 2 TiO 3 . The particle size and the morphology found in the Li 2 TiO 3 , showed similar particle size and morphology to the TiO 2 used as precursor. (Author)

  8. Synthesis and sintering Ni-Zn ferrite obtained for combustion reaction in large scale

    International Nuclear Information System (INIS)

    Vieira, D.A.; Diniz, V.C.S.; Costa, A.C.F.M.; Cornejo, D.R.; Kiminami, R.H.G.A.

    2014-01-01

    This research proposes to evaluate the magnetic properties of ferrite Ni-Zn synthesized by combustion reaction on a large scale and sintered at 1250 deg C in resistive furnace. The sample was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and magnetic measurements. The results show that the synthesized product in large scale resulted in soft magnetic material with saturation magnetization of 40 emu·g"-"1 and coercivity of 0.080 kOe, after sintering it was observed an increase to 68 emu·g"-"1 in the magnetization and a reduction to 0.016 kOe in coercivity, indicating that the obtained material has promising characteristics for applications in electro-electronic devices. (author)

  9. A novel rhombohedron-like nickel ferrite nanostructure: Microwave combustion synthesis, structural characterization and magnetic properties

    Directory of Open Access Journals (Sweden)

    G. Suresh Kumar

    2016-09-01

    Full Text Available Research on nickel ferrite nanostructures has drawn a great interest because of its inherent chemical, physical and electronic properties. In this study, we have synthesized rhombohedron – like nickel ferrite nanostructure by a rapid microwave assisted combustion method using ethylenediamminetetraacetic acid as a chelating agent. X-ray diffraction, Fourier transform infrared spectrometer, transmission electron microscope and energy dispersive X-ray microanalyser were used to characterize the prepared sample. The magnetic behaviour was analysed by means of field dependent magnetization measurement which indicates that the prepared sample exhibits a soft ferromagnetic nature with saturation magnetization of 63.034 emu/g. This technique can be a potential method to synthesize novel nickel ferrite nanostructure with improved magnetic properties.

  10. Solution combustion method for synthesis of nanostructured hydroxyapatite, fluorapatite and chlorapatite

    Science.gov (United States)

    Zhao, Junjie; Dong, Xiaochen; Bian, Mengmeng; Zhao, Junfeng; Zhang, Yao; Sun, Yue; Chen, JianHua; Wang, XuHong

    2014-09-01

    Hydroxyapatite (HAP), fluorapatite (Fap) and chlorapatite (Clap) were prepared by solution combustion method with further annealing at 800 °C. The characterization and structural features of the synthesized powders were evaluated by the powder X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM) and transmission electron microscopy (TEM) techniques. Characterization results from XRD and Rietveld analysis revealed that OH- in the HAP lattice were gradually substituted with the increase of F- and Cl- content and totally substituted at the molar concentration of 0.28 and 0.6, respectively. The results from FI-IR have also confirmed the incorporation of substituted anions in the apatite structure.

  11. Bulk synthesis of nanocrystalline urania powders by citrate gel-combustion method

    Science.gov (United States)

    Sanjay Kumar, D.; Ananthasivan, K.; Venkata Krishnan, R.; Amirthapandian, S.; Dasgupta, Arup

    2016-01-01

    Bulk quantities (60 g) of nanocrystalline (nc) free flowing urania powders with crystallite size ranging from 38 to 252 nm have been synthesized for the first time by the citrate gel combustion method. A systematic study of the influence of the fuel (citric acid) to oxidant (nitrate) ratio (R) on the characteristics of the urania powders has been carried out for the first time. Mixture with an "R" value of 0.25 exhibited a vigorous auto-ignition reaction. This reaction was investigated with Differential Scanning Calorimetry (DSC) and in-situ thermogravimetry coupled with differential thermal analysis and mass spectrometry (TG-DTA-MS). The bulk density, specific surface area, X-ray crystallite size, residual carbon and size distribution of particles of this powder were unique. Microscopic and microstructural investigation of selected samples revealed the presence of nanocrystals with irregular exfoliated morphology; their Electron Energy Loss Spectra testified the covalency of the U-O bond.

  12. Combustion synthesis of MgO nanoparticles using plant extract: Structural characterization and photoluminescence studies

    Science.gov (United States)

    Kumar, Danith; Yadav, L. S. Reddy; Lingaraju, K.; Manjunath, K.; Suresh, D.; Prasad, Daruka; Nagabhushana, H.; Sharma, S. C.; Naika, H. Raja; Chikkahanumantharayappa, Nagaraju, G.

    2015-06-01

    Magnesium oxide nanoparticles (MgO Nps) have been successfully synthesized via solution combustion method using Parthenium plant extract as fuel for the first time. Powder X-ray diffraction (PXRD) pattern reveal that product belongs to the cubic phase (Periclase). FTIR spectrum shows the band at 822 cm-1 indicates the formation of cubic periclase MgO. The optical band gap of MgO Nps estimated from UV -Vis spectrum was found to be in the range 5.40-5.45 eV. SEM images showed that, the product is agglomerated and particle in nature. Photoluminescence (PL) studies shows violet emission at 390 nm, blue emission at 470 nm and green emission at 550 nm. MgO Nps shows good photocatalytic activity for the degradation of methylene blue (MB) dye under UV/Sun light irradiation.

  13. Combustion synthesis of MgO nanoparticles using plant extract: Structural characterization and photoluminescence studies

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Danith; Chikkahanumantharayappa [Dept. of Physics, Vivekananda First grade College, Bangalore - 560055 (India); Yadav, L. S. Reddy; Nagaraju, G., E-mail: nagarajugn@rediffmail.com [Dept of Chemistry, Siddaganga Institute of Technology, Tumkur, Karnataka-572103 (India); Lingaraju, K.; Naika, H. Raja [Dept. of Environmental Science, Tumkur University, Tumkur, Karnataka-572103 (India); Manjunath, K. [Centre for Nano and Material Sciences, Jain University, Jakkasandra, Karnataka-562112 (India); Suresh, D. [Dept. of Chemistry, Tumkur University, Tumkur, Karnataka-572103 (India); Prasad, Daruka [Dept. of Physics, BMS Institute of Technology, Bangalore-560064 (India); Nagabhushana, H. [CNR Rao Center for Advanced Materials, Tumkur University, Tumkur, Karnataka-572103 (India); Sharma, S. C. [Chattisgarh Swami Vivekananda Technological University, Bhilai, Chattisgarh-490009 (India)

    2015-06-24

    Magnesium oxide nanoparticles (MgO Nps) have been successfully synthesized via solution combustion method using Parthenium plant extract as fuel for the first time. Powder X-ray diffraction (PXRD) pattern reveal that product belongs to the cubic phase (Periclase). FTIR spectrum shows the band at 822 cm{sup −1} indicates the formation of cubic periclase MgO. The optical band gap of MgO Nps estimated from UV –Vis spectrum was found to be in the range 5.40–5.45 eV. SEM images showed that, the product is agglomerated and particle in nature. Photoluminescence (PL) studies shows violet emission at 390 nm, blue emission at 470 nm and green emission at 550 nm. MgO Nps shows good photocatalytic activity for the degradation of methylene blue (MB) dye under UV/Sun light irradiation.

  14. Combustion synthesis of MgO nanoparticles using plant extract: Structural characterization and photoluminescence studies

    International Nuclear Information System (INIS)

    Kumar, Danith; Chikkahanumantharayappa; Yadav, L. S. Reddy; Nagaraju, G.; Lingaraju, K.; Naika, H. Raja; Manjunath, K.; Suresh, D.; Prasad, Daruka; Nagabhushana, H.; Sharma, S. C.

    2015-01-01

    Magnesium oxide nanoparticles (MgO Nps) have been successfully synthesized via solution combustion method using Parthenium plant extract as fuel for the first time. Powder X-ray diffraction (PXRD) pattern reveal that product belongs to the cubic phase (Periclase). FTIR spectrum shows the band at 822 cm −1 indicates the formation of cubic periclase MgO. The optical band gap of MgO Nps estimated from UV –Vis spectrum was found to be in the range 5.40–5.45 eV. SEM images showed that, the product is agglomerated and particle in nature. Photoluminescence (PL) studies shows violet emission at 390 nm, blue emission at 470 nm and green emission at 550 nm. MgO Nps shows good photocatalytic activity for the degradation of methylene blue (MB) dye under UV/Sun light irradiation

  15. Synthesis, structure and electromagnetic properties of Mn–Zn ferrite by sol–gel combustion technique

    International Nuclear Information System (INIS)

    Wang, Wenjie; Zang, Chongguang; Jiao, Qingjie

    2014-01-01

    The electromagnetic absorbing behaviors of a thin coating fabricated by mixing Mn–Zn ferrite with epoxy resin (EP) were studied. The spinel ferrites Mn 1−x Zn x Fe 2 O 4 (x=0.2, 0.5 and 0.8) were synthesized with citrate acid as complex agent by sol–gel combustion method. The microstructure and surface morphology of Mn–Zn ferrite powders were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). The complex permittivity and complex permeability of the fabricated ferrite/EP composites were investigated in terms of their contributions to the absorbing properties in the low frequency (10 MHz to 1 GHz). The microwave absorption of the prepared ferrite/EP composites could be tailored by matching the dielectric loss and magnetic loss and by controlling the doped metal ratio. The composites with the ferrite composition x=0.2 are found to show higher reflection loss compared with the composites with other compositions. It is proposed that the prepared composites can potentially be applied in electromagnetic microwave absorbing field. - Highlights: • We designed and synthesized Mn 1−x Zn x Fe 2 O 4 (x=0.2, 0.5 and 0.8), with citrate acid as complex agent by the sol–gel combustion method. • Citrate acid as the complex agent overcomes the aggregation of ferrite resulting in high purity and homogeneous particles. • We investigated the electromagnetic absorbing performance of a fabricated thin coating by introducing Mn–Zn ferrite into epoxy resin (EP). • The Mn 0.8 Zn 0.2 Fe 2 O 4 composite coatings could achieve the satisfactory absorbing value of −17 dB at 800 MHz. • The prepared composites can potentially be used for the application in electromagnetic microwave absorbing field

  16. Histidine as a catalyst in organic synthesis: A facile in situ synthesis ...

    Indian Academy of Sciences (India)

    Unknown

    They are also used in the synthesis of many nitrogen-containing biologically ... addition to hydroxylamine, results in formation of an imine, azoxy compound 15, ... GC-MS, m/z: 211 (M+), 194 (base peak); 13C NMR (DMSO-d6) δ : 31⋅14 ...

  17. Facile EG/ionic liquid interfacial synthesis of uniform RE(3+) doped NaYF(4) nanocubes.

    Science.gov (United States)

    Zhang, Chao; Chen, Ji

    2010-01-28

    Uniform multicolor upconversion luminescent RE(3+) doped NaYF(4) nanocubes are fabricated through a facile ethylene glycol (EG)/ionic liquid interfacial synthesis route at 80 degrees C, with the ionic liquids acting as both reagents and templates.

  18. Aerosol Combustion Synthesis of Nanopowders and Processing to Functional Thin Films

    Science.gov (United States)

    Yi, Eongyu

    In this dissertation, the advantages of liquid-feed flame spray pyrolysis (LF-FSP) process in producing nanoparticles (NPs) as well as processing the produced NPs to ceramic/polymer nanocomposite films and high density polycrystalline ceramic films are demonstrated. The LF-FSP process aerosolizes alcohol solutions of metalloorganic precursors by oxygen and combusts them at > 1500 °C. The combustion products are rapidly quenched ( 10s of ms) to green and potentially lower cost alternative. We then show the versatility of NPs in formulating flexible ceramic/polymer nanocomposites (BaTiO3/epoxy) with superior properties. Volume fractions of the BaTiO3 filler and composite film thicknesses were controlled to adjust the net dielectric constant and the capacitance. Measured net dielectric constants further deviated from theory, with increasing solids loadings, due to NP agglomeration. Wound nanocomposite capacitors showed ten times higher capacitance compared to the commercial counterpart. Following series of studies explore the use of flame made NPs in processing Li+ conducting membranes. Systematic doping studies were conducted in the LiTi2(PO4)3 system to modify the lattice constant, conduction channel width, and sintering behavior by introducing Al3+ and Si4+ dopants. Excess Li2O content was also adjusted to observe its effect on final microstructures and phase compositions. Improved densification rates were found in Li1.7 Al0.3Ti1.7Si0.4P2.6O 12 composition and thin films (52+/-1 microm) with conductivities of 0.3-0.5 mS cm-1 were achieved. Li6.25M0.25La3Zr2O12 (M = Al3+, Ga3+) thin films (25-28 microm) with conductivities of 0.2-1.3 mS cm-1 were also successfully processed using flame made NPs, overcoming processing challenges extant, resulting in significantly reduced energy input required for densification. Heating schedules, sintering atmospheres, and types of substrates were controlled to observe their effect on the sintering behavior. Furthermore, green film

  19. A microwave-assisted solution combustion synthesis to produce europium-doped calcium phosphate nanowhiskers for bioimaging applications.

    Science.gov (United States)

    Wagner, Darcy E; Eisenmann, Kathryn M; Nestor-Kalinoski, Andrea L; Bhaduri, Sarit B

    2013-09-01

    Biocompatible nanoparticles possessing fluorescent properties offer attractive possibilities for multifunctional bioimaging and/or drug and gene delivery applications. Many of the limitations with current imaging systems center on the properties of the optical probes in relation to equipment technical capabilities. Here we introduce a novel high aspect ratio and highly crystalline europium-doped calcium phosphate nanowhisker produced using a simple microwave-assisted solution combustion synthesis method for use as a multifunctional bioimaging probe. X-ray diffraction confirmed the material phase as europium-doped hydroxyapatite. Fluorescence emission and excitation spectra and their corresponding peaks were identified using spectrofluorimetry and validated with fluorescence, confocal and multiphoton microscopy. The nanowhiskers were found to exhibit red and far red wavelength fluorescence under ultraviolet excitation with an optimal peak emission of 696 nm achieved with a 350 nm excitation. Relatively narrow emission bands were observed, which may permit their use in multicolor imaging applications. Confocal and multiphoton microscopy confirmed that the nanoparticles provide sufficient intensity to be utilized in imaging applications. Copyright © 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

  20. Enhanced Photoluminescence of Sm3+/Bi3+ Co-Doped La2O3 Nanophosphors by Combustion Synthesis

    Science.gov (United States)

    Zhang, Ying; Wu, Muying; Zhang, W. F.

    Nanosized La2O3:Sm3+ and La2O3:Sm3+, Bi3+ phosphor powders were prepared via combustion synthesis. The structures and morphology were examined using powder X-ray diffraction and transmission electron microscope, respectively. The photoluminescence spectra were investigated at different doping concentrations of Sm3+ and Bi3+ ions. The results indicate that La2O3:Sm3+ (Bi3+) exhibited good crystallinity and spherical-like particles. All phosphors give emission bands centered at 564, 608 and 650 nm corresponding to 4G5/2→6HJ (J=5/2, 7/2 and 9/2) transitions of Sm3+ ions, respectively. Interestingly, the emission intensity of Sm3+ ions is significantly enhanced with the addition of Bi3+ ions to La2O3:Sm3+ and the maximum occurs at a Bi3+ concentration of 0.8 mol%. The La2O3:Sm3+, Bi3+ phosphor with highly enhanced luminescence is very encouraging for applications in display and tunable solid lasers.

  1. Auto-combustion synthesis, Mössbauer study and catalytic properties of copper-manganese ferrites

    International Nuclear Information System (INIS)

    Velinov, N.; Petrova, T.; Tsoncheva, T.; Genova, I.; Koleva, K.; Kovacheva, D.; Mitov, I.

    2016-01-01

    Spinel ferrites with nominal composition Cu _0_._5Mn _0_._5Fe _2O_4 and different distribution of the ions are obtained by auto-combustion method. Mössbauer spectroscopy, X-ray Diffraction, Thermogravimetry-Differential Scanning Calorimetry, Scanning Electron Microscopy and catalytic test in the reaction of methanol decomposition is used for characterization of synthesized materials. The spectral results evidence that the phase composition, microstructure of the synthesized materials and the cation distribution depend on the preparation conditions. Varying the pH of the initial solution microstructure, ferrite crystallite size, cation oxidation state and distribution of ions in the in the spinel structure could be controlled. The catalytic behaviour of ferrites in the reaction of methanol decomposition also depends on the pH of the initial solution. Reduction transformations of mixed ferrites accompanied with the formation of Hägg carbide χ-Fe _5C_2 were observed by the influence of the reaction medium.

  2. Highly porous CeO2 nanostructures prepared via combustion synthesis for supercapacitor applications

    DEFF Research Database (Denmark)

    Kadirvelayutham, Prasanna; Santhoshkumar, P.; Jo, Yong Nam

    2017-01-01

    We report highly porous CeO2 nanostructures (CeO2 NSs) suitable for supercapacitor applications, synthesized using a fast and cost effective combustion approach. Due to its prominent valence states of Ce3+/Ce4+, CeO2 has emerged as a promising pseudocapacitive material. The drawback of using CeO2...... as a supercapacitor electrode is its poor electrical conductivity. We overcame this drawback of CeO2 by creating oxygen vacancies on its surface, which act to enhance its electrical conductivity. The physical interpretation of the as-synthesized CeO2 NSs shows that they have dense active sites and diffusion pathways...... that enhance the performance of the electrode in a supercapacitor. Electrodes prepared using the synthesized CeO2 NSs exhibited the initial specific capacitance of 134.6 F g-1 and superior cycling stability of 92.5% after 1000 cycles at a constant current density of 1 A g-1, indicating their potential...

  3. Thermoluminescence of novel zinc oxide nano phosphors obtained by glycine-based solution combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Orante B, V. R.; Escobar O, F. M.; Cruz V, C. [Universidad de Sonora, Departamento de Investigacion en Polimeros y Materiales, Apdo. Postal 130, 83000 Hermosillo, Sonora (Mexico); Bernal, R., E-mail: victor.orante@polimeros.uson.mx [Universidad de Sonora, Departamento de Investigacion en Fisica, Apdo. Postal 5-088, 83190 Hermosillo, Sonora (Mexico)

    2015-10-15

    Full text: High-dose thermoluminescence dosimetry properties of novel zinc oxide nano phosphors synthesized by a solution combustion method in a glycine-nitrate process are presented for the very first time in this work. Sintered particles with sizes ranging between ∼500 nm and ∼2 μm were obtained by annealing the synthesized Zn O at 900 degrees C during 2 h in air. X-ray diffraction patterns indicate the presence of the Zn O hexagonal phase, without any remaining nitrate peaks observed. Thermoluminescence glow curves of Zn O obtained after being exposed to beta radiation consists of two maxima: one located at ∼ 149 degrees C and another at ∼ 308 degrees C, the latter being the dosimetric component of the curve. The integrated Tl fading displays an asymptotic behaviour for times longer than 16 h between irradiation and the corresponding Tl readout, as well as a linear behaviour of the dose response without saturation in the studied dose interval (from 12.5 up to 400 Gy). Such features place synthesized Zn O as a promising material for high-dose radiation dosimetry applications. (Author)

  4. Thermoluminescence of novel zinc oxide nano phosphors obtained by glycine-based solution combustion synthesis

    International Nuclear Information System (INIS)

    Orante B, V. R.; Escobar O, F. M.; Cruz V, C.; Bernal, R.

    2015-10-01

    Full text: High-dose thermoluminescence dosimetry properties of novel zinc oxide nano phosphors synthesized by a solution combustion method in a glycine-nitrate process are presented for the very first time in this work. Sintered particles with sizes ranging between ∼500 nm and ∼2 μm were obtained by annealing the synthesized Zn O at 900 degrees C during 2 h in air. X-ray diffraction patterns indicate the presence of the Zn O hexagonal phase, without any remaining nitrate peaks observed. Thermoluminescence glow curves of Zn O obtained after being exposed to beta radiation consists of two maxima: one located at ∼ 149 degrees C and another at ∼ 308 degrees C, the latter being the dosimetric component of the curve. The integrated Tl fading displays an asymptotic behaviour for times longer than 16 h between irradiation and the corresponding Tl readout, as well as a linear behaviour of the dose response without saturation in the studied dose interval (from 12.5 up to 400 Gy). Such features place synthesized Zn O as a promising material for high-dose radiation dosimetry applications. (Author)

  5. Synthesis, structure and electromagnetic properties of Mn-Zn ferrite by sol-gel combustion technique

    Science.gov (United States)

    Wang, Wenjie; Zang, Chongguang; Jiao, Qingjie

    2014-01-01

    The electromagnetic absorbing behaviors of a thin coating fabricated by mixing Mn-Zn ferrite with epoxy resin (EP) were studied. The spinel ferrites Mn1-xZnxFe2O4 (x=0.2, 0.5 and 0.8) were synthesized with citrate acid as complex agent by sol-gel combustion method. The microstructure and surface morphology of Mn-Zn ferrite powders were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). The complex permittivity and complex permeability of the fabricated ferrite/EP composites were investigated in terms of their contributions to the absorbing properties in the low frequency (10 MHz to 1 GHz). The microwave absorption of the prepared ferrite/EP composites could be tailored by matching the dielectric loss and magnetic loss and by controlling the doped metal ratio. The composites with the ferrite composition x=0.2 are found to show higher reflection loss compared with the composites with other compositions. It is proposed that the prepared composites can potentially be applied in electromagnetic microwave absorbing field.

  6. Green synthesis of magnetic chitosan nanocomposites by a new sol–gel auto-combustion method

    Energy Technology Data Exchange (ETDEWEB)

    Ansari, Fatemeh [Institute of Nano Science and Nano Technology, University of Kashan, P.O. Box. 87317–51167, Kashan, Islamic Republic of Iran (Iran, Islamic Republic of); Sobhani, Azam [Department of Chemistry, Kosar University of Bojnord, Bojnord, Islamic Republic of Iran (Iran, Islamic Republic of); Salavati-Niasari, Masoud, E-mail: salavati@kashanu.ac.ir [Institute of Nano Science and Nano Technology, University of Kashan, P.O. Box. 87317–51167, Kashan, Islamic Republic of Iran (Iran, Islamic Republic of)

    2016-07-15

    The Fe{sub 2}O{sub 3}/CuFe{sub 2}O{sub 4}/chitosan nanocomposites have been successfully synthesized via a new sol–gel auto-combustion route. To prepare the nanocomposites, copper ferrite (CuFe{sub 2}O{sub 4}) and iron (II) oxide (Fe{sub 2}O{sub 3}) nanostructures were first prepared utilizing onion as a green reductant for the first time, and characterized by SEM, TEM, XRD, IR and VSM. Then chitosan was added into the nanostructures dispersed in water. Chitosan was used to functionalize and modify the nanostructures and also to improve surface properties. The nanocomposites were also characterized by several techniques including SEM, TEM, XRD, IR and VSM. The effects of amount of onion and chitosan on the morphology and particle size of nanocomposites were evaluated. - Highlights: • Fe{sub 2}O{sub 3}/CuFe{sub 2}O{sub 4}/chitosan nanocomposites were synthesized for the first time. • A simple, low-cost and friendly route was used to synthesize the nanocomposites. • Effects of amount of onion and chitosan were investigated.

  7. Auto-combustion synthesis, Mössbauer study and catalytic properties of copper-manganese ferrites

    Energy Technology Data Exchange (ETDEWEB)

    Velinov, N., E-mail: nikivelinov@ic.bas.bg; Petrova, T. [Institute of Catalysis, Bulgarian Academy of Sciences (Bulgaria); Tsoncheva, T.; Genova, I. [Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences (Bulgaria); Koleva, K. [Institute of Catalysis, Bulgarian Academy of Sciences (Bulgaria); Kovacheva, D. [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences (Bulgaria); Mitov, I. [Institute of Catalysis, Bulgarian Academy of Sciences (Bulgaria)

    2016-12-15

    Spinel ferrites with nominal composition Cu {sub 0.5}Mn {sub 0.5}Fe {sub 2}O{sub 4} and different distribution of the ions are obtained by auto-combustion method. Mössbauer spectroscopy, X-ray Diffraction, Thermogravimetry-Differential Scanning Calorimetry, Scanning Electron Microscopy and catalytic test in the reaction of methanol decomposition is used for characterization of synthesized materials. The spectral results evidence that the phase composition, microstructure of the synthesized materials and the cation distribution depend on the preparation conditions. Varying the pH of the initial solution microstructure, ferrite crystallite size, cation oxidation state and distribution of ions in the in the spinel structure could be controlled. The catalytic behaviour of ferrites in the reaction of methanol decomposition also depends on the pH of the initial solution. Reduction transformations of mixed ferrites accompanied with the formation of Hägg carbide χ-Fe {sub 5}C{sub 2} were observed by the influence of the reaction medium.

  8. Synthesis of lithium silicates generators of tritium by a modified method of combustion; Sintesis de silicatos de litio generadores de tritio por un metodo modificado de combustion

    Energy Technology Data Exchange (ETDEWEB)

    Cruz G, D

    2003-07-01

    The ceramics of lithium have been proposed as generating materials of tritium through the following reaction: {sup 6} Li + {sup 1} n {yields} {sup 4} He + {sup 3} H . In previous works carried out by Pfeiffer and collaborators, the lithium silicates generators of tritium were prepared using the following methods: reactions of solid state, precipitation and sol-gel synthesis. Although those methods have advantages, it is required of heating at high temperatures (900 C during four hours) to be able to obtain the crystalline compounds. Those products found in these works were diverse crystallization forms of the lithium silicates and of SiO{sub 2}, such as, Li{sub 2}SiO{sub 3}, Li{sub 2}Si{sub 2}0{sub 5}, Li{sub 4}SiO{sub 4}, and quartz (SiO{sub 2}). The combustion method uses exothermic reactions to take place ceramic compounds. The precursor solutions are mixtures of the nitrate of metal oxidizer and the fuels (urea, glycine, carbohydrazide). However the reported method in the literature, it is not useful to prepare lithium silicates, for what was modified using non oxidizers compounds. The lithium hydroxide (LiOH) and the silicic acid (H{sub 2}SiO{sub 3}) they were the compounds non oxidizers used, and the urea (CH{sub 4}N{sub 2}O) it was the one fuel. They were carried out two series of experiments; inside the series 1 of experiments are varied the molar ratio of lithium hydroxide and urea (LiOH : H{sub 2}SiO{sub 3} = 1, 2 and 3, LiOH : CH{sub 4}N{sub 2}O = 1, 2, 3, 4 and 5) and the prepared mixtures were taken to one muffle previously preheated to a temperature of 450 C during 5 minutes. In the series 2 of experiments was studied the effect of the temperature and of the washed with distilled water in the prepared samples with the following molar ratios: LiOH : H{sub 2}SiO{sub 3} : CH{sub 4}N{sub 2}O = 1:1:3, 2:1:3, 3:1:3 and 3:1:6, those which were heated to temperatures from 450 C up to 750 C and were washed. The obtained samples were characterized by X

  9. La{sub 2-x}Sr{sub x}NiO{sub 4+{delta}} ceramic powders prepared by combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Colomer, M.T.; Chinarro, E.; Jurado, J.R. [Consejo Nacional de Investigaciones Cientificas, Madrid (Spain). Ist. de Ceramica y Vidrio

    2002-07-01

    Combustion synthesis provides an attractive method of producing ceramic powders because of its low cost, process simplicity and fastness. Materials based on La{sub 2}NiO{sub 4+{delta}} can be successfully prepared by combustion synthesis. La{sub 2-x}Sr{sub x}NiO{sub 4+{delta}} (x = 0, 0.1) accommodates oxygen excess by oxygen interstitials rather than by the more usual cation vacancies. A high concentration of oxygen interstitials offers the possibility of rapid oxygen transport through the ceramic material and thus provide a new type of mixed ionic-electronic conductor. The fast oxide ion diffusion combined with its thermal stability indicate that these materials would be good candidates for use in ceramic oxygen generators (COGs) and intermediate temperature solid oxide fuel cells (IT-SOFCs). The present work discusses a combustion synthesis technique to prepare La{sub 2-x}Sr{sub x}NiO{sub 4+{delta}} (x = 0, 0.1) powders using the corresponding metal nitrates-urea mixtures, at low temperature and short reaction times. The as-prepared combustion powders were characterized by XRD, DTA-TG, SEM/TEM-EDX and BET. La{sub 2-x}Sr{sub x}NiO{sub 4} (x = 0, 0.1) powders with a good compositional control and homogeneity are attained. The as-prepared powders obtained at 300 C (ignition temperature) showed much higher specific surface area than powders obtained via alternative routes and contained La{sub 2-x}Sr{sub x}NiO{sub 4+{delta}}, as the major phase present, together with La{sub 2}O{sub 3} and a small amount of NiO. La{sub 2-x}Sr{sub x}NiO{sub 4+{delta}} single phase is achieved, respectively at 950 C for x =0.1 and at 975 C for x = 0. (orig.)

  10. Facile radiolytic synthesis of ruthenium nanoparticles on graphene oxide and carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Rojas, J.V., E-mail: jvrojas@vcu.edu [Mechanical and Nuclear Engineering Department, Virginia Commonwealth University, 401 West Main Street, Richmond, Virginia, 23284 (United States); Toro-Gonzalez, M.; Molina-Higgins, M.C. [Mechanical and Nuclear Engineering Department, Virginia Commonwealth University, 401 West Main Street, Richmond, Virginia, 23284 (United States); Castano, C.E., E-mail: cecastanolond@vcu.edu [Nanomaterials Core Characterization Facility, Chemical and Life Science Engineering Department, Virginia Commonwealth University, 601 West Main Street, Richmond, Virginia, 23284 (United States)

    2016-03-15

    Graphical abstract: - Highlights: • Facile radiolytic synthesis of Ru nanoparticles on graphene oxide and carbon nanotubes. • Homogeneously distributed Rh nanoparticles on supports are ∼2.5 nm in size. • Simultaneous reduction of graphene oxide and Ru ions occurs during the synthesis. • Ru-O bonds evidenced the interaction of the nanoparticles with the support. - Abstract: Ruthenium nanoparticles on pristine (MWCNT) and functionalized carbon nanotubes (f-MWCNT), and graphene oxide have been prepared through a facile, single step radiolytic method at room temperature, and ambient pressure. This synthesis process relies on the interaction of high energy gamma rays from a {sup 60}Co source with the water in the aqueous solutions containing the Ru precursor, leading to the generation of highly reducing species that further reduce the Ru metal ions to zero valence state. Transmission electron microscopy and X-Ray diffraction revealed that the nanoparticles were homogeneously distributed on the surface of the supports with an average size of ∼2.5 nm. X-ray Photoelectron spectroscopy analysis showed that the interaction of the Ru nanoparticles with the supports occurred through oxygenated functionalities, creating metal-oxygen bonds. This method demonstrates to be a simple and clean approach to produce well dispersed nanoparticles on the aforementioned supports without the need of any hazardous chemical.

  11. Facile radiolytic synthesis of ruthenium nanoparticles on graphene oxide and carbon nanotubes

    International Nuclear Information System (INIS)

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

    2016-01-01

    Graphical abstract: - Highlights: • Facile radiolytic synthesis of Ru nanoparticles on graphene oxide and carbon nanotubes. • Homogeneously distributed Rh nanoparticles on supports are ∼2.5 nm in size. • Simultaneous reduction of graphene oxide and Ru ions occurs during the synthesis. • Ru-O bonds evidenced the interaction of the nanoparticles with the support. - Abstract: Ruthenium nanoparticles on pristine (MWCNT) and functionalized carbon nanotubes (f-MWCNT), and graphene oxide have been prepared through a facile, single step radiolytic method at room temperature, and ambient pressure. This synthesis process relies on the interaction of high energy gamma rays from a "6"0Co source with the water in the aqueous solutions containing the Ru precursor, leading to the generation of highly reducing species that further reduce the Ru metal ions to zero valence state. Transmission electron microscopy and X-Ray diffraction revealed that the nanoparticles were homogeneously distributed on the surface of the supports with an average size of ∼2.5 nm. X-ray Photoelectron spectroscopy analysis showed that the interaction of the Ru nanoparticles with the supports occurred through oxygenated functionalities, creating metal-oxygen bonds. This method demonstrates to be a simple and clean approach to produce well dispersed nanoparticles on the aforementioned supports without the need of any hazardous chemical.

  12. Facile and green synthesis of highly stable L-cysteine functionalized copper nanoparticles

    International Nuclear Information System (INIS)

    Kumar, Nikhil; Upadhyay, Lata Sheo Bachan

    2016-01-01

    Highlights: • A facile and eco-friendly method for the synthesis of L-cysteine functionalized copper nanoparticles is reported. • Synthesis of Highly stable L-cysteine functionalized copper nanoparticles (∼40 nm) was done in an aqueous medium. • FTIR analysis shows that L-cysteine bound to the nanoparticle surface via thiol group. - Abstract: A simple eco-friendly method for L-cysteine capped copper nanoparticles (CCNPs) synthesis in aqueous solution has been developed. Glucose and L-cysteine were used as reducing agent and capping/functionalizing agent, respectively. Different parameters such as capping agent concentration, pH, reaction temperature, and reducing agent concentration were optimized during the synthesis. The L-cysteine capped copper nanoparticle were characterized by ultraviolet-visible spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, Particle size and zeta potential analyser, and high resolution transmission electron microscopy. Spherical shaped cysteine functionalized/capped copper nanoparticles with an average size of 40 nm were found to be highly stable at room temperature (RT) for a period of 1 month

  13. Facile and green synthesis of highly stable L-cysteine functionalized copper nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Nikhil, E-mail: nkumar.phd2011.bt@nitrr.ac.in; Upadhyay, Lata Sheo Bachan, E-mail: contactlataupadhyay@gmail.com

    2016-11-01

    Highlights: • A facile and eco-friendly method for the synthesis of L-cysteine functionalized copper nanoparticles is reported. • Synthesis of Highly stable L-cysteine functionalized copper nanoparticles (∼40 nm) was done in an aqueous medium. • FTIR analysis shows that L-cysteine bound to the nanoparticle surface via thiol group. - Abstract: A simple eco-friendly method for L-cysteine capped copper nanoparticles (CCNPs) synthesis in aqueous solution has been developed. Glucose and L-cysteine were used as reducing agent and capping/functionalizing agent, respectively. Different parameters such as capping agent concentration, pH, reaction temperature, and reducing agent concentration were optimized during the synthesis. The L-cysteine capped copper nanoparticle were characterized by ultraviolet-visible spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, Particle size and zeta potential analyser, and high resolution transmission electron microscopy. Spherical shaped cysteine functionalized/capped copper nanoparticles with an average size of 40 nm were found to be highly stable at room temperature (RT) for a period of 1 month.

  14. Conventional and microwave combustion synthesis of optomagnetic CuFe2O4 nanoparticles for hyperthermia studies

    Science.gov (United States)

    Kombaiah, K.; Vijaya, J. Judith; Kennedy, L. John; Bououdina, M.; Al-Najar, Basma

    2018-04-01

    Nanosized copper ferrite (CuFe2O4) nanoparticles have been prepared by conventional (CCM) and microwave (MCM) combustion methods using Hibiscus rosa sinensis plant extract as a fuel. XRD and rietveld analysis confirmed the formation of single cubic phase and with crystallite size varying from 25 to 62 nm owing to grain growth after calcination. FT-IR analysis confirms the modes of the cubic CuFe2O4 phase, due to the stretching and bending vibrations. Spherical shaped particles are observed by scanning electron microscopy and the average particle size is found to be in the range of 50-200 nm. The chemical composition is confirmed by energy dispersive X-ray analysis. The optical band gap energy estimated using Kubelka-Munk function with the help of UV-Visible diffused reflectance spectroscopy, is found to be 2.34 and 2.22 eV for CCM and MCM respectively. Photoluminescence analysis indicates that both samples absorb light in the UV-visible region and exhibit emissions at 360, 376, and 412 nm. Magnetic measurements indicate a ferromagnetic behavior, where both magnetic properties very much influenced by the preparation method and calcination temperature: both saturation magnetization and coercivity are found higher when using CCM and MCM; from 29.40 to 34.09 emu/g while almost double from 224.4 to 432.2 Oe. The observed changes in physical properties are mainly associated with crystallinity, particle size, better chemical homogeneity, and cations distribution among tetrahedral/octahedral sites. The maximum specific absorption rate obtained was 14.63 W/g, which can be considered suitable and favorable for magnetic hyperthermia. This study highlighted the benefits of green synthesis of CuFe2O4 nanoparticles providing better magnetic properties for the platform of hyperthermia application.

  15. Gold icosahedral nanocages: Facile synthesis, optical properties, and fragmentation under ultrasonication

    Science.gov (United States)

    Yang, Xuan; Gilroy, Kyle D.; Vara, Madeline; Zhao, Ming; Zhou, Shan; Xia, Younan

    2017-09-01

    Because of their unique optical properties, gold nanocages are excellent candidates for biomedical applications. Traditionally, they are prepared using a method that involves the galvanic replacement reaction between Ag nanocubes and HAuCl4. Here we demonstrate a different approach for the facile synthesis of Au icosahedral nanocages containing twin boundaries, as well as a compact size below 15 nm and ultrathin walls of only a few atomic layers thick. Their optical properties could be tuned by simply controlling the etching time, a result that was also validated by computational modeling. We further evaluated the feasibility of fragmenting the nanocages using ultrasonication.

  16. Facile Synthesis of Novel Nanostructured MnO2Thin Films and Their Application in Supercapacitors

    Directory of Open Access Journals (Sweden)

    Xia H

    2009-01-01

    Full Text Available Abstract Nanostructured α-MnO2thin films with different morphologies are grown on the platinum substrates by a facile solution method without any assistance of template or surfactant. Microstructural characterization reveals that morphology evolution from dandelion-like spheres to nanoflakes of the as-grown MnO2is controlled by synthesis temperature. The capacitive behavior of the MnO2thin films with different morphologies are studied by cyclic voltammetry. The α-MnO2thin films composed of dandelion-like spheres exhibit high specific capacitance, good rate capability, and excellent long-term cycling stability.

  17. Facile Synthesis of Colloidal CuO Nanocrystals for Light-Harvesting Applications

    KAUST Repository

    Lim, Yee-Fun; Choi, Joshua J.; Hanrath, Tobias

    2012-01-01

    CuO is an earth-abundant, nontoxic, and low band-gap material; hence it is an attractive candidate for application in solar cells. In this paper, a synthesis of CuO nanocrystals by a facile alcohothermal route is reported. The nanocrystals are dispersible in a solvent mixture of methanol and chloroform, thus enabling the processing of CuO by solution. A bilayer solar cell comprising of CuO nanocrystals and phenyl-C61-butyric acid methyl ester (PCBM) achieved a power conversion efficiency of 0.04%, indicating the potential of this material for light-harvesting applications.

  18. Mascotte, a research test facility for high pressure combustion of cryogenic propellants; Mascotte, un banc d'essai de recherche pour la combustion a haute pression d'ergols cryogeniques

    Energy Technology Data Exchange (ETDEWEB)

    Vingert, L.; Habiballah, M.; Traineau, J.C. [Office National d' Etudes et de Recherches Aerospatiales (ONERA), 92 - Chatillon (France)

    2000-07-01

    Detailed experimental studies of cryogenic propellant combustion are needed to improve design and optimization of high performance liquid rocket engines. A research test facility called Mascotte has been built up by ONERA to study elementary processes that are involved in the combustion of liquid oxygen and gaseous hydrogen. Mascotte is aimed at feeding a single element combustor with actual propellants, and the third version in operation since mid 1998 allows to reach supercritical pressures in the combustor. A specific high pressure combustor was developed for this purpose. Research teams from different laboratories belonging to CNRS and ONERA, regrouped in a common research program managed by CNES and SNECMA division SEP, may run experiments on Mascotte, with several objectives: - improve the knowledge and the modeling of physical phenomena; - provide experimental results for computer code validation; - improve and assess diagnostic techniques (especially optical diagnostics). Following diagnostics for instance, were used on Mascotte from 1994 to 1999: - OH imaging (spontaneous emission and laser induced fluorescence ); - CARS temperature measurements (using the H{sub 2} and simultaneously the H{sub 2}O molecules); - High speed cinematography (with a copper vapor laser synchronized to a high speed camera); - O{sub 2} vapor imaging (laser induced fluorescence); - Particle sizing (by means of a Phase Doppler Particle Analyzer). (authors)

  19. Structural, morphological and optical investigations on BaMgAl10O17:Eu2+ elaborated by a microwave induced solution combustion synthesis

    International Nuclear Information System (INIS)

    Pradal, Nathalie; Potdevin, Audrey; Chadeyron, Genevieve; Mahiou, Rachid

    2011-01-01

    Graphical abstract: Graphical abstract (with Research highlights). This is a paragraph for graphical abstract. Research highlights: → Synthesis of BAM:Eu 2+ by MISCS using different fuel to oxidizer molar ratios. → Both blue and red phosphors were obtained. → Majority of blue phosphors was obtained for fuel-rich synthesis. → A specific morphology was observed for each contribution. -- Abstract: Blue-emitting Eu 2+ -doped barium magnesium aluminate (BaMgAl 10 O 17 :Eu 2+ ) for advanced displays and lighting devices was prepared by a microwave induced solution combustion synthesis using urea as combustion fuel and nitrates as oxidizer. Purity control of as-synthesized blue phosphor particles was undertaken by modifying the fuel to oxidizer molar ratio. X-ray diffraction, scanning electron microscopy and photoluminescence were used to investigate powders crystallinity, particles size, morphology and luminescent properties, respectively. Fuel-rich urea reactions preferentially lead to pure phases compared to the powders synthesized with a stoichiometric fuel to oxidizer ratio. In both cases, we produce a nearly pure well-crystallized and nanostructured BaMgAl 10 O 17 :Eu 2+ . Photoluminescence measurements exhibit the characteristic blue emission of Eu 2+ under UV light excitation however a weak red emission associated to Eu 3+ is also detected.

  20. Ultrafast one-step combustion synthesis and thermoelectric properties of In-doped Cu{sub 2}SnSe{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yuyang [Key Laboratory of Cryogenics, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190 (China); University of Chinese Academy of Sciences, Beijing, 100049 (China); Liu, Guanghua, E-mail: liugh02@163.com [Key Laboratory of Cryogenics, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190 (China); Li, Jiangtao, E-mail: lijiangtao@mail.ipc.ac.cn [Key Laboratory of Cryogenics, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190 (China); Chen, Kexin [State Key Laboratory of New Ceramics & Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing, 100084 (China); He, Gang; Yang, Zengchao; Han, Yemao; Zhou, Min; Li, Laifeng [Key Laboratory of Cryogenics, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190 (China)

    2016-07-01

    Bulk In-doped Cu{sub 2}SnSe{sub 3} samples were prepared by a fast and one-step method of high-gravity combustion synthesis. All the synthesized samples were dense with relative densities of >98%. The influence of Indium-doping on the phase composition of the samples was investigated. SEM and EDS measurements confirm the existence of SnSe and Cu{sub 2}Se as secondary phase in the Cu{sub 2}Sn{sub 1−x}In{sub x}Se{sub 3} samples. In addition, the experimental results show that there is a solubility limit of indium in the Cu{sub 2}SnSe{sub 3} matrix. The thermoelectric properties of the samples were measured in a temperature range from 323 K to 773 K, and the Cu{sub 2}Sn{sub 0.8}In{sub 0.2}Se{sub 3} sample achieved a maximum ZT of 0.65 at 773 K, which was comparable with the best-reported result for Cu{sub 2}SnSe{sub 3} materials prepared by conventional sintering approaches. With much reduced time and energy consumption, high-gravity combustion synthesis may offer a more efficient and economical way for producing thermoelectric materials. - Highlights: • Dense bulk Cu{sub 2}SnSe{sub 3} materials are prepared by one-step combustion synthesis. • The solubility limit of Indium into the Cu{sub 2}SnSe{sub 3} matrix has been discussed. • A maximum ZT of 0.65 is obtained for the Cu{sub 2}Sn{sub 1−x}In{sub x}Se{sub 3} (x = 0.2) at 773 K.

  1. Photon up-conversion production in Tb{sup 3+}–Yb{sup 3+} co-doped CaF{sub 2} phosphors prepared by combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Rakov, Nikifor, E-mail: nikifor.gomez@univasf.edu.br [PG—Ciência dos Materiais, Universidade Federal do Vale do São Francisco, 48902-300 Juazeiro, BA (Brazil); Guimarães, Renato B. [Instituto de Física, Universidade Federal Fluminense, 24210-346 Niterói, RJ (Brazil); Maciel, Glauco S., E-mail: glauco@if.uff.br [Instituto de Física, Universidade Federal Fluminense, 24210-346 Niterói, RJ (Brazil)

    2016-02-15

    Graphical abstract: Up-conversion luminescence from Tb{sup 3+} obtained by energy transfer from Yb{sup 3+} pairs in CaF{sub 2} powder prepared by combustion synthesis. - Highlights: • Calcium fluoride (CaF{sub 2}) powders were prepared by combustion synthesis. • Rare-earth ions doped in this material were found in interstitial sites. • Cooperative up-conversion was observed in Tb{sup 3+}:Yb{sup 3+}:CaF{sub 2} powder. • Energy transfer between Tb{sup 3+} and pairs of Yb{sup 3+} was analyzed using rate equations. - Abstract: Calcium fluoride (CaF{sub 2}) crystalline powders were successfully prepared by the combustion synthesis method. The powder material containing luminescent rare-earth ions, more specifically terbium (Tb{sup 3+}) and ytterbium (Yb{sup 3+}), was studied by X-ray diffraction, scanning electronic microscopy and optical spectroscopy. These ions are allocated in charge compensated interstitial positions of tetragonal (C{sub 4v}) and trigonal (C{sub 3v}) symmetry sites of the cubic (O{sub h}) CaF{sub 2} lattice. Up-conversion (UC) luminescence in Tb{sup 3+} was achieved using a low power diode laser operating at 975 nm. Tb{sup 3+} is insensitive to near-infrared radiation but UC can be achieved via energy transfer from pairs of Yb{sup 3+} ions to Tb{sup 3+} ions. The UC luminescence dynamics of Tb{sup 3+} was used to study the energy transfer mechanism.

  2. Hydrogen storage properties of Mg-23.3wt.%Ni eutectic alloy prepared via hydriding combustion synthesis followed by mechanical milling

    International Nuclear Information System (INIS)

    Liquan Li; Yunfeng Zhu; Xiaofeng Liu

    2006-01-01

    A Mg-23.3wt.%Ni eutectic alloy was prepared by the process of hydriding combustion synthesis followed by mechanical milling (HCS+MM). The product showed a high hydriding rate at 373 K and the dehydrogenation started at temperature as low as 423 K. Several reasons contributing to the improvement in hydrogen storage properties were presented. The result of this study will provide attractive information for mobile applications of magnesium hydrogen storage materials, and the process of HCS+MM developed in this study showed its potential for synthesizing magnesium based hydrogen storage materials with novel hydriding/de-hydriding properties. (authors)

  3. Microwave combustion synthesis of in situ Al{sub 2}O{sub 3} and Al{sub 3}Zr reinforced aluminum matrix composites

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Heguo, E-mail: zhg1200@sina.com [College of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Key Laboratory of Advanced Micro-Nano Materials and Technology, Jiangsu Province Higher Education Institutions, 210094 (China); Synergetic Center for Advanced Materials Research, Jiangsu Province Higher Education Institutions, 210094 (China); Hua, Bo; Cui, Tao; Huang, Jiewen; Li, Jianliang [College of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Xie, Zonghan, E-mail: zonghan.xie@adelaide.edu.au [School of Mechanical & Electrical Engineering, Wuhan Institute of Technology, Wuhan 430073 (China); School of Mechanical Engineering, University of Adelaide, SA 5005 (Australia)

    2015-08-15

    Al{sub 2}O{sub 3} and Al{sub 3}Zr reinforced aluminum matrix composites were fabricated from Al and ZrO{sub 2} powders by SiC assisted microwave combustion synthesis. The microstructure and reaction pathways were analyzed by using differential scanning calorimetry (DSC), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS). The results showed that the heating rate during microwave synthesis was very high and the entire process took several minutes and that the ignition temperature of the reaction was much lower than that of conventional methods. In addition, the resulting microstructure was found to be finer than that prepared by the conventional methods and no cracks can be seen in the Al{sub 3}Zr reinforcements. As such, the newly developed composites have potential for safety-critical applications where catastrophic failure is not tolerated.

  4. Lump wood combustion process

    Science.gov (United States)

    Kubesa, Petr; Horák, Jiří; Branc, Michal; Krpec, Kamil; Hopan, František; Koloničný, Jan; Ochodek, Tadeáš; Drastichová, Vendula; Martiník, Lubomír; Malcho, Milan

    2014-08-01

    The article deals with the combustion process for lump wood in low-power fireplaces (units to dozens of kW). Such a combustion process is cyclical in its nature, and what combustion facility users are most interested in is the frequency, at which fuel needs to be stoked to the fireplace. The paper defines the basic terms such as burnout curve and burning rate curve, which are closely related to the stocking frequency. The fuel burning rate is directly dependent on the immediate thermal power of the fireplace. This is also related to the temperature achieved in the fireplace, magnitude of flue gas losses and the ability to generate conditions favouring the full burnout of the fuel's combustible component, which, at once ensures the minimum production of combustible pollutants. Another part of the paper describes experiments conducted in traditional fireplaces with a grate, at which well-dried lump wood was combusted.

  5. Evaluation of solution combustion method in the synthesis of Fe-ZrSiO4 based coral pigment

    International Nuclear Information System (INIS)

    Moosavi, A.; Aghaei, A.

    2008-01-01

    Auto-ignited gel combustion process has been used for producing a red hematite-zircon based pigment. The combustible mixtures contained the metal nitrates and citric acid as oxidizers and fuel, respectively. Sodium silicate (water glass) was used as silica source for producing zircon phase. X-Ray Diffractometry, Electron Microscopy and Simultaneous Thermal Analysis were used for characterization of reactions happened in the resulted dried gel during its heat-treatment. L*a*b* color parameters were measured by the CIE (Commission International de I'Eclairage) colorimetric method. This research has showed that solution combustion was unable 10 produce coral pigment as the end product of combustion without the need for any further heat treatment process

  6. Template-Assisted Wet-Combustion Synthesis of Fibrous Nickel-Based Catalyst for Carbon Dioxide Methanation and Methane Steam Reforming.

    Science.gov (United States)

    Aghayan, M; Potemkin, D I; Rubio-Marcos, F; Uskov, S I; Snytnikov, P V; Hussainova, I

    2017-12-20

    Efficient capture and recycling of CO 2 enable not only prevention of global warming but also the supply of useful low-carbon fuels. The catalytic conversion of CO 2 into an organic compound is a promising recycling approach which opens new concepts and opportunities for catalytic and industrial development. Here we report about template-assisted wet-combustion synthesis of a one-dimensional nickel-based catalyst for carbon dioxide methanation and methane steam reforming. Because of a high temperature achieved in a short time during reaction and a large amount of evolved gases, the wet-combustion synthesis yields homogeneously precipitated nanoparticles of NiO with average particle size of 4 nm on alumina nanofibers covered with a NiAl 2 O 4 nanolayer. The as-synthesized core-shell structured fibers exhibit outstanding activity in steam reforming of methane and sufficient activity in carbon dioxide methanation with 100% selectivity toward methane formation. The as-synthesized catalyst shows stable operation under the reaction conditions for at least 50 h.

  7. Combustion synthesis as a novel approach in preparation of polycrystalline Y{sub 2}Cu{sub 2}O{sub 5}

    Energy Technology Data Exchange (ETDEWEB)

    Gebrel, Z., E-mail: z_gebrel@yahoo.com; Blanusa, J.; Spasojevic, V.; Kusigerski, V.; Mrakovic, A.; Alqat, A.; Perovic, M.

    2013-08-15

    Highlights: •Y{sub 2}Cu{sub 2}O{sub 5} was successfully synthesized by both the glycine–nitrate and SHS method. •The reduction of synthesis duration down to 12 h has been achieved. •The detailed crystal structure and magnetic analyses of obtained material are provided. -- Abstract: Polycrystalline samples of Y{sub 2}Cu{sub 2}O{sub 5} were for the first time sintered from precursors obtained by two combustion routes – the glycine–nitrate method (sample S1) and a modified self-propagating high-temperature synthesis (sample S2). The detailed X-ray diffraction analysis has confirmed that both samples are well crystallized and single phase, with the high crystallization degree and cation ordering within a Cu sublattice. Magnetic characterization has shown magnetic behavior typical of pure Y{sub 2}Cu{sub 2}O{sub 5}. The distinctive advantages of these new synthesis routes in comparison to the ceramic sintering are in simplification of the overall procedure as well as in a significant reduction of synthesis duration from several days down to 31 h (S1) or 12 h (S2)

  8. Synthesis of SrBi{sub 2}Ta{sub 2}O{sub 9} by combustion synthesis; Obtencao do SrBi{sub 2}Ta{sub 2}O{sub 9} utilizando a sintese por combustao

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, F.F.; Bergmann, C.P. [Universidade Federal do Rio Grande do Sul (LACER/UFRGS), Porto Alegre, RS (Brazil). Dept. de Materiais. Lab. de Materiais Ceramicos; Sousa, V.C. [Universidade Federal do Rio Grande do Sul (LABIOMAT/UFRGS), Porto Alegre, RS (Brazil). Dept. de Materiais. Lab. de Materiais de Biomateriais

    2009-07-01

    The combustion synthesis is a low cost technique for obtaining homogeneous nanostructured compounds with high purity. The ferroelectric memory devices have been widely studied by the electronics industry by presenting high-speed recording, read and rewrite. The PZT, in the form of thin films, is the ceramic materials most used for this purpose, but it presents ferroelectric fatigue. The SrBi{sub 2}Ta{sub 2}O{sub 9} has a high cycle enables the recording which is good applicability in the PZT. Therefore, this work aims to obtain the SrBi{sub 2}Ta{sub 2}O{sub 9} using the combustion synthesis and urea as a reducing agent. The characterization of the powder was realized used the technique of x-ray diffraction (XRD) to determine the phases present and to evaluate surface area by the BET method. The powder obtained after synthesis showed low crystallinity presenting just the BiOCl like the crystalline phase present, but heat treatment at 800 deg C for 2 hours was sufficient for the formation of SrBi{sub 2}Ta{sub 2}O{sub 9} . (author)

  9. Scalable Synthesis of Triple-Core-Shell Nanostructures of TiO2 @MnO2 @C for High Performance Supercapacitors Using Structure-Guided Combustion Waves.

    Science.gov (United States)

    Shin, Dongjoon; Shin, Jungho; Yeo, Taehan; Hwang, Hayoung; Park, Seonghyun; Choi, Wonjoon

    2018-03-01

    Core-shell nanostructures of metal oxides and carbon-based materials have emerged as outstanding electrode materials for supercapacitors and batteries. However, their synthesis requires complex procedures that incur high costs and long processing times. Herein, a new route is proposed for synthesizing triple-core-shell nanoparticles of TiO 2 @MnO 2 @C using structure-guided combustion waves (SGCWs), which originate from incomplete combustion inside chemical-fuel-wrapped nanostructures, and their application in supercapacitor electrodes. SGCWs transform TiO 2 to TiO 2 @C and TiO 2 @MnO 2 to TiO 2 @MnO 2 @C via the incompletely combusted carbonaceous fuels under an open-air atmosphere, in seconds. The synthesized carbon layers act as templates for MnO 2 shells in TiO 2 @C and organic shells of TiO 2 @MnO 2 @C. The TiO 2 @MnO 2 @C-based electrodes exhibit a greater specific capacitance (488 F g -1 at 5 mV s -1 ) and capacitance retention (97.4% after 10 000 cycles at 1.0 V s -1 ), while the absence of MnO 2 and carbon shells reveals a severe degradation in the specific capacitance and capacitance retention. Because the core-TiO 2 nanoparticles and carbon shell prevent the deformation of the inner and outer sides of the MnO 2 shell, the nanostructures of the TiO 2 @MnO 2 @C are preserved despite the long-term cycling, giving the superior performance. This SGCW-driven fabrication enables the scalable synthesis of multiple-core-shell structures applicable to diverse electrochemical applications. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Synthesis, structural investigation and magnetic properties of Zn2+ substituted cobalt ferrite nanoparticles prepared by the sol–gel auto-combustion technique

    International Nuclear Information System (INIS)

    Raut, A.V.; Barkule, R.S.; Shengule, D.R.; Jadhav, K.M.

    2014-01-01

    Structural morphology and magnetic properties of the Co 1−x Zn x Fe 2 O 4 (0.0≤x≥1.0) spinel ferrite system synthesized by the sol–gel auto-combustion technique using nitrates of respective metal ions have been studied. The ratio of metal nitrates to citric acid was taken at 1:3. The as prepared powder of cobalt zinc ferrite was sintered at 600 °C for 12 h after TG/DTA thermal studies. Compositional stoichiometry was confirmed by energy dispersive analysis of the X-ray (EDAX) technique. Single phase cubic spinel structure of Co–Zn nanoparticles was confirmed by XRD data. The average crystallite size (t), lattice constant (a) and other structural parameters of zinc substituted cobalt ferrite nanoparticles were calculated from XRD followed by SEM and FTIR. It is observed that the sol–gel auto-combustion technique has many advantages for the synthesis of technologically applicable Co–Zn ferrite nanoparticles. The present investigation clearly shows the effect of the synthesis method and possible relation between magnetic properties and microstructure of the prepared samples. Increase in nonmagnetic Zn 2+ content in cobalt ferrite nanoparticles is followed by decrease in n B , M s and other magnetic parameters. Squareness ratio for the Co-ferrite was 1.096 at room temperature. - Highlights: • Co–Zn nanoparticles are prepared by sol–gel auto-combustion method. • Structural properties were characterized by XRD, SEM, and FTIR. • Compositional stoichiometry was confirmed by EDAX analysis. • Magnetic parameters were measured by the pulse field hysteresis loop technique

  11. Synthesis, structural investigation and magnetic properties of Zn{sup 2+} substituted cobalt ferrite nanoparticles prepared by the sol–gel auto-combustion technique

    Energy Technology Data Exchange (ETDEWEB)

    Raut, A.V., E-mail: nano9993@gmail.com [Vivekanand Arts and Sardar Dalipsingh Commerce and Science College, Aurangabad, 431004 Maharastra (India); Barkule, R.S.; Shengule, D.R. [Vivekanand Arts and Sardar Dalipsingh Commerce and Science College, Aurangabad, 431004 Maharastra (India); Jadhav, K.M., E-mail: drjadhavkm@gmail.com [Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, 431004 Maharastra (India)

    2014-05-01

    Structural morphology and magnetic properties of the Co{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} (0.0≤x≥1.0) spinel ferrite system synthesized by the sol–gel auto-combustion technique using nitrates of respective metal ions have been studied. The ratio of metal nitrates to citric acid was taken at 1:3. The as prepared powder of cobalt zinc ferrite was sintered at 600 °C for 12 h after TG/DTA thermal studies. Compositional stoichiometry was confirmed by energy dispersive analysis of the X-ray (EDAX) technique. Single phase cubic spinel structure of Co–Zn nanoparticles was confirmed by XRD data. The average crystallite size (t), lattice constant (a) and other structural parameters of zinc substituted cobalt ferrite nanoparticles were calculated from XRD followed by SEM and FTIR. It is observed that the sol–gel auto-combustion technique has many advantages for the synthesis of technologically applicable Co–Zn ferrite nanoparticles. The present investigation clearly shows the effect of the synthesis method and possible relation between magnetic properties and microstructure of the prepared samples. Increase in nonmagnetic Zn{sup 2+} content in cobalt ferrite nanoparticles is followed by decrease in n{sub B}, M{sub s} and other magnetic parameters. Squareness ratio for the Co-ferrite was 1.096 at room temperature. - Highlights: • Co–Zn nanoparticles are prepared by sol–gel auto-combustion method. • Structural properties were characterized by XRD, SEM, and FTIR. • Compositional stoichiometry was confirmed by EDAX analysis. • Magnetic parameters were measured by the pulse field hysteresis loop technique.

  12. One-Step Facile Synthesis of a Simple Hole Transport Material for Efficient Perovskite Solar Cells

    KAUST Repository

    Chen, Hu

    2016-04-04

    A hole transporting material was designed for use in perovskite solar cells, with a facile one-step synthesis from inexpensive, com-mercially available reagents. The molecule comprises a central fluorinated phenyl core with pendant aryl amines, namely, 3,6-difluoro-N1,N1,N2,N2,N4,N4,N5,N5-octakis(4-methoxyphenyl)benzene-1,2,4,5-tetraamine (DFTAB). A power conversion efficiency of up to 10.4% was achieved in a mesoporous perovskite device architecture. The merits of a simple and potentially low cost syn-thetic route as well as promising performance in perovskite devices, encourages further development of this materials class as new low-cost hole transporting materials for the scale up of perovskite solar cells.

  13. Facile and template-free method toward chemical synthesis of polyaniline film/nanotube structures

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Pei [Department of Electrical and Computer Engineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh Pennsylvania 15261; Zhu, Yisi [Materials Science Division, Argonne National Lab, Lemont Illinois 60439; Torres, Jorge [Department of Electrical and Computer Engineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh Pennsylvania 15261; Lee, Seung Hee [Department of BIN Fusion Technology, Chonbuk National University, Jeonju 561-786 Korea; Yun, Minhee [Department of Electrical and Computer Engineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh Pennsylvania 15261

    2017-09-05

    A facile and template-free method is reported to synthesize a new thin film structure: polyaniline (PANI) film/nanotubes (F/N) structure. The PANI F/N is a 100-nm thick PANI film embedded with PANI nanotubes. This well-controlled method requires no surfactant or organic acid as well as relatively low concentration of reagents. Synthesis condition studies reveal that aniline oligomers with certain structures are responsible for guiding the growth of the nanotubes. Electrical characterization also indicates that the PANI F/N possesses similar field-effect transistor characteristics to bare PANI film. With its 20% increased surface-area-to-volume (S/V) ratio contributed by surface embedded nanotubes and the excellent p-type semiconducting characteristic, PANI F/N shows clear superiority compared with bare PANI film. Such advantages guarantee the PANI F/N a promising future toward the development of ultra-high sensitivity and low-cost biosensors.

  14. Controlled Synthesis of Manganese Dioxide Nano structures via a Facile Hydrothermal

    International Nuclear Information System (INIS)

    Pang, R.S.C.; Chin, S.F.; Ye, Ch. Ling

    2012-01-01

    Manganese dioxide nano structures with controllable morphological structures and crystalline phases were synthesized via a facile hydrothermal route at low temperatures without using any templates or surfactants. Both the aging duration and aging temperatures were the main synthesis parameters used to influence and control the rate of morphological and structural evolution of MnO 2 nano structures. MnO 2 nano structures comprise of spherical nano particulate agglomerates and highly amorphous in nature were formed at lower temperature and/or short aging duration. In contrast, MnO 2 nano structures of sea-urchin-like and nano rods-like morphologies and nanocrystalline in nature were prepared at the combined higher aging temperatures and longer aging durations. These nano structures underwent notable phase transformation from d-MnO 2 to a-MnO 2 upon prolonged hydrothermal aging duration and exhibited accelerated rate of phase transformation at higher aging temperature.

  15. Facile synthesis of nanostructured transition metal oxides as electrodes for Li-ion batteries

    Science.gov (United States)

    Opra, Denis P.; Gnedenkov, Sergey V.; Sokolov, Alexander A.; Minaev, Alexander N.; Kuryavyi, Valery G.; Sinebryukhov, Sergey L.

    2017-09-01

    At all times, energy storage is one of the greatest scientific challenge. Recently, Li-ion batteries are under special attention due to high working voltage, long cycle life, low self-discharge, reliability, no-memory effect. However, commercial LIBs usage in medium- and large-scale energy storage are limited by the capacity of lithiated metal oxide cathode and unsafety of graphite anode at high-rate charge. In this way, new electrode materials with higher electrochemical performance should be designed to satisfy a requirement in both energy and power. As it known, nanostructured transition metal oxides are promising electrode materials because of their elevated specific capacity and high potential vs. Li/Li+. In this work, the perspective of an original facile technique of pulsed high-voltage plasma discharge in synthesis of nanostructured transition metal oxides as electrodes for lithium-ion batteries has been demonstrated.

  16. Facile synthesis of graphene on dielectric surfaces using a two-temperature reactor CVD system

    International Nuclear Information System (INIS)

    Zhang, C; Man, B Y; Yang, C; Jiang, S Z; Liu, M; Chen, C S; Xu, S C; Sun, Z C; Gao, X G; Chen, X J

    2013-01-01

    Direct deposition of graphene on a dielectric substrate is demonstrated using a chemical vapor deposition system with a two-temperature reactor. The two-temperature reactor is utilized to offer sufficient, well-proportioned floating Cu atoms and to provide a temperature gradient for facile synthesis of graphene on dielectric surfaces. The evaporated Cu atoms catalyze the reaction in the presented method. C atoms and Cu atoms respectively act as the nuclei for forming graphene film in the low-temperature zone and the zones close to the high-temperature zones. A uniform and high-quality graphene film is formed in an atmosphere of sufficient and well-proportioned floating Cu atoms. Raman spectroscopy, scanning electron microscopy and atomic force microscopy confirm the presence of uniform and high-quality graphene. (paper)

  17. Facile and High-Yielding Synthesis of TAM Biradicals and Monofunctional TAM Radicals.

    Science.gov (United States)

    Trukhin, Dmitry V; Rogozhnikova, Olga Yu; Troitskaya, Tatiana I; Vasiliev, Vladimir G; Bowman, Michael K; Tormyshev, Victor M

    2016-04-01

    Facile and high-yielding procedures for synthesis of monocarboxylic acid derivatives of triarylmethyl radicals (TAMs) were developed. Reaction of methyl thioglycolate with tris(2,3,5,6-tetrathiaaryl)methyl cation smoothly afforded the monosubstituted TAM derivative, which was hydrolyzed to a monocarboxylic acid, with the TAM moiety attached to thioglycolic acid via the sulfur atom. Alternatively, the diamagnetic tricarboxylic acid precursor of Finland trityl was transformed to a trimethyl ester and partially hydrolyzed under controlled conditions. The diester product was isolated and the remaining fractions were converted back to the trimethyl ester for production of more diester. The first representatives of TAM biradicals with different TAM cores and interspin distances were obtained by reaction of these new TAM monocaboxylic acids with N,N'-dimethylethylenediamine.

  18. One-Step Facile Synthesis of a Simple Hole Transport Material for Efficient Perovskite Solar Cells

    KAUST Repository

    Chen, Hu; Bryant, Daniel; Troughton, Joel; Kirkus, Mindaugas; Neophytou, Marios; Miao, Xiaohe; Durrant, James R.; McCulloch, Iain

    2016-01-01

    A hole transporting material was designed for use in perovskite solar cells, with a facile one-step synthesis from inexpensive, com-mercially available reagents. The molecule comprises a central fluorinated phenyl core with pendant aryl amines, namely, 3,6-difluoro-N1,N1,N2,N2,N4,N4,N5,N5-octakis(4-methoxyphenyl)benzene-1,2,4,5-tetraamine (DFTAB). A power conversion efficiency of up to 10.4% was achieved in a mesoporous perovskite device architecture. The merits of a simple and potentially low cost syn-thetic route as well as promising performance in perovskite devices, encourages further development of this materials class as new low-cost hole transporting materials for the scale up of perovskite solar cells.

  19. Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst.

    Science.gov (United States)

    Yeow, Jonathan; Xu, Jiangtao; Boyer, Cyrille

    2016-06-08

    Presented herein is a protocol for the facile synthesis of worm-like micelles by visible light mediated dispersion polymerization. This approach begins with the synthesis of a hydrophilic poly(oligo(ethylene glycol) methyl ether methacrylate) (POEGMA) homopolymer using reversible addition-fragmentation chain-transfer (RAFT) polymerization. Under mild visible light irradiation (λ = 460 nm, 0.7 mW/cm(2)), this macro-chain transfer agent (macro-CTA) in the presence of a ruthenium based photoredox catalyst, Ru(bpy)3Cl2 can be chain extended with a second monomer to form a well-defined block copolymer in a process known as Photoinduced Electron Transfer RAFT (PET-RAFT). When PET-RAFT is used to chain extend POEGMA with benzyl methacrylate (BzMA) in ethanol (EtOH), polymeric nanoparticles with different morphologies are formed in situ according to a polymerization-induced self-assembly (PISA) mechanism. Self-assembly into nanoparticles presenting POEGMA chains at the corona and poly(benzyl methacrylate) (PBzMA) chains in the core occurs in situ due to the growing insolubility of the PBzMA block in ethanol. Interestingly, the formation of highly pure worm-like micelles can be readily monitored by observing the onset of a highly viscous gel in situ due to nanoparticle entanglements occurring during the polymerization. This process thereby allows for a more reproducible synthesis of worm-like micelles simply by monitoring the solution viscosity during the course of the polymerization. In addition, the light stimulus can be intermittently applied in an ON/OFF manner demonstrating temporal control over the nanoparticle morphology.

  20. Facile synthesis of a silver nanoparticles/polypyrrole nanocomposite for non-enzymatic glucose determination.

    Science.gov (United States)

    Poletti Papi, Maurício A; Caetano, Fabio R; Bergamini, Márcio F; Marcolino-Junior, Luiz H

    2017-06-01

    The present work describes the synthesis of a new conductive nanocomposite based on polypyrrole (PPy) and silver nanoparticles (PPy-AgNP) based on a facile reverse microemulsion method and its application as a non-enzymatic electrochemical sensor for glucose detection. Focusing on the best sensor performance, all experimental parameters used in the synthesis of nanocomposite were optimized based on its electrochemical response for glucose. Characterization of the optimized material by FT-IR, cyclic voltammetry, and DRX measurements and TEM images showed good monodispersion of semispherical Ag nanoparticles capped by PPy structure, with size average of 12±5nm. Under the best analytical conditions, the proposed sensor exhibited glucose response in linear dynamic range of 25 to 2500μmolL -1 , with limit of detection of 3.6μmolL -1 . Recovery studies with human saliva samples varying from 99 to 105% revealed the accuracy and feasibility of a non-enzymatic electrochemical sensor for glucose determination by easy construction and low-cost. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Healthy food procurement and nutrition standards in public facilities: evidence synthesis and consensus policy recommendations

    Directory of Open Access Journals (Sweden)

    Kim D. Raine

    2018-01-01

    Full Text Available Introduction: Unhealthy foods are widely available in public settings across Canada, contributing to diet-related chronic diseases, such as obesity. This is a concern given that public facilities often provide a significant amount of food for consumption by vulnerable groups, including children and seniors. Healthy food procurement policies, which support procuring, distributing, selling, and/or serving healthier foods, have recently emerged as a promising strategy to counter this public health issue by increasing access to healthier foods. Although numerous Canadian health and scientific organizations have recommended such policies, they have not yet been broadly implemented in Canada. Methods: To inform further policy action on healthy food procurement in a Canadian context, we: (1 conducted an evidence synthesis to assess the impact of healthy food procurement policies on health outcomes and sales, intake, and availability of healthier food, and (2 hosted a consensus conference in September 2014. The consensus conference invited experts with public health/nutrition policy research expertise, as well as health services and food services practitioner experience, to review evidence, share experiences, and develop a consensus statement/recommendations on healthy food procurement in Canada. Results: Findings from the evidence synthesis and consensus recommendations for healthy food procurement in Canada are described. Specifically, we outline recommendations for governments, publicly funded institutions, decision-makers and professionals, citizens, and researchers. Conclusion: Implementation of healthy food procurement policies can increase Canadians’ access to healthier foods as part of a broader vision for food policy in Canada.

  2. Facile, one-step controlled synthesis of Se nanocrystals in the presence of L-tyrosine

    International Nuclear Information System (INIS)

    Wang Xiufang; Zhang Weiqiang; Shen Yuhua; Xie Anjian; Huang Lachun

    2011-01-01

    Highlights: → Se was synthesized via a novel and facile pathway. → The morphologies and the crystalline phases of Se can be easily controlled. → Tyrosine is excellent reducing agent and soft template for the synthesis of Se. → It is possible to provide an excellent route to obtain nanomaterials. - Abstract: Se with different morphologies was synthesized using L-tyrosine as reducing agent and soft template by means of hydrothermal method. The method was simple and convenient to handle. The reaction process was monitored using ultraviolet-visible spectroscopy (UV-vis) and Fourier-transform infrared spectroscopy (FTIR). The morphology and crystalline phase were determined by transmission electron microscopy (TEM), scanning electronic microscopy (SEM) and X-ray diffraction (XRD) pattern. The results show that the morphologies and the crystalline phases of Se can be easily controlled. By varying the concentration ratio of L-tyrosine to selenious acid, the morphologies and crystalline phases of Se were not changed, but the diameter of Se was different. Se nano-rods are obtained in the lower temperature, and there is a transformation of microspheres into nanorods of Se with the increase of reaction time or reaction temperature. In addition, we discuss the possible mechanism of the reduction of SeO 3 2- ions by L-tyrosine. The eco-friendly, biogenic synthesis strategy could be widely used for preparing inorganic/organic biocomposites.

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

    International Nuclear Information System (INIS)

    Joseph, Siby; Mathew, Beena

    2015-01-01

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

  4. Healthy food procurement and nutrition standards in public facilities: evidence synthesis and consensus policy recommendations

    Science.gov (United States)

    Kim D., Raine; Kayla, Atkey; Dana Lee, Dana Lee; Alexa R., Ferdinands; Dominique, Beaulieu; Susan, Buhler; Norm, Campbell; Brian, Cook; Mary, L’Abbé; Ashley, Lederer; David, Mowat; Joshna, Maharaj; Candace, Nykiforuk; Jacob, Shelley; Jacqueline, Street

    2018-01-01

    Abstract Introduction: Unhealthy foods are widely available in public settings across Canada, contributing to diet-related chronic diseases, such as obesity. This is a concern given that public facilities often provide a significant amount of food for consumption by vulnerable groups, including children and seniors. Healthy food procurement policies, which support procuring, distributing, selling, and/or serving healthier foods, have recently emerged as a promising strategy to counter this public health issue by increasing access to healthier foods. Although numerous Canadian health and scientific organizations have recommended such policies, they have not yet been broadly implemented in Canada. Methods: To inform further policy action on healthy food procurement in a Canadian context, we: (1) conducted an evidence synthesis to assess the impact of healthy food procurement policies on health outcomes and sales, intake, and availability of healthier food, and (2) hosted a consensus conference in September 2014. The consensus conference invited experts with public health/nutrition policy research expertise, as well as health services and food services practitioner experience, to review evidence, share experiences, and develop a consensus statement/recommendations on healthy food procurement in Canada. Results: Findings from the evidence synthesis and consensus recommendations for healthy food procurement in Canada are described. Specifically, we outline recommendations for governments, publicly funded institutions, decision-makers and professionals, citizens, and researchers. Conclusion: Implementation of healthy food procurement policies can increase Canadians’ access to healthier foods as part of a broader vision for food policy in Canada. PMID:29323862

  5. Silver nanoparticles with gelatin nanoshells: photochemical facile green synthesis and their antimicrobial activity

    International Nuclear Information System (INIS)

    Pourjavadi, Ali; Soleyman, Rouhollah

    2011-01-01

    In the current study, a facile green synthesis of silver-gelatin core–shell nanostructures (spherical, spherical/cubic hybrid, and cubic, DLS diameter: 4.1–6.9 nm) is reported via the wet chemical synthesis procedure. Sunlight-UV as an available reducing agent cause mild reduction of silver ions into the silver nanoparticles (Ag-NPs). Gelatin protein, as an effective capping/shaping agent, was used in the reaction to self-assemble silver nanostructures. The formation of silver nanostructures and their self-assembly pattern was confirmed by SEM, AFM, and TEM techniques. Further investigations were carried out using zeta-potential, UV–Vis, FTIR, GPC, and TGA/DTG/DTA data. The prepared Ag-NPs showed proper and acceptable antimicrobial activity against three classes of microorganisms (Escherichia coli Gram-negative bacteria, Staphylococcus aureus Gram-positive bacteria, and Candida albicans fungus). The antibacterial and antifungal Ag-NPs exhibit good stability in solution and can be considered as promising candidates for a wide range of biomedical applications.

  6. Silver nanoparticles with gelatin nanoshells: photochemical facile green synthesis and their antimicrobial activity

    Science.gov (United States)

    Pourjavadi, Ali; Soleyman, Rouhollah

    2011-10-01

    In the current study, a facile green synthesis of silver-gelatin core-shell nanostructures (spherical, spherical/cubic hybrid, and cubic, DLS diameter: 4.1-6.9 nm) is reported via the wet chemical synthesis procedure. Sunlight-UV as an available reducing agent cause mild reduction of silver ions into the silver nanoparticles (Ag-NPs). Gelatin protein, as an effective capping/shaping agent, was used in the reaction to self-assemble silver nanostructures. The formation of silver nanostructures and their self-assembly pattern was confirmed by SEM, AFM, and TEM techniques. Further investigations were carried out using zeta-potential, UV-Vis, FTIR, GPC, and TGA/DTG/DTA data. The prepared Ag-NPs showed proper and acceptable antimicrobial activity against three classes of microorganisms ( Escherichia coli Gram-negative bacteria, Staphylococcus aureus Gram-positive bacteria, and Candida albicans fungus). The antibacterial and antifungal Ag-NPs exhibit good stability in solution and can be considered as promising candidates for a wide range of biomedical applications.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-05-15

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

  8. Microwave combustion synthesis of hexagonal prism shaped ZnO nanoparticles and effect of Cr on structural, optical and electrical properties of ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Yathisha, R.O. [Department of Chemistry, School of Chemical Sciences, Kuvempu University, Jnanasahyadri, Shankaraghatta 577 451, Karnataka (India); Nayaka, Y. Arthoba, E-mail: drarthoba@yahoo.co.in [Department of Chemistry, School of Chemical Sciences, Kuvempu University, Jnanasahyadri, Shankaraghatta 577 451, Karnataka (India); Vidyasagar, C.C. [Department of Chemistry, School of Basic Sciences, Ranichannamma University, Belgaum 591156, Karnataka (India)

    2016-09-15

    The synthesis and study of semiconducting nanostructure materials have become a considerable interdisciplinary area of research over the past few decades. The control of morphologies and effective doping by right dopant are the two tasks for the synthesis of semiconducting nanoparticles. The present work outlines the synthesis of ZnO and Cr-ZnO nanoparticles via microwave combustion method without using any fuel. The crystal morphology, optical and electrical properties were characterized by X-ray diffraction study (XRD), UV–Visible spectroscopy (UV–Vis), Scanning electron microscopy (SEM), Energy-dispersive analysis using X-rays (EDAX), Transmission electron microscopy (TEM) and Keithley source meter. The crystal size was determined from XRD, whose values were found to be decreased with increase in the concentration of Cr up to 2 wt% and further increase in the dopant concentration resulted the formation secondary phase (ZnCr{sub 2}O{sub 4}). Scanning electron micrographs shows the hexagonal prism structure of ZnO and Cr-ZnO nanoparticles. EDAX shows the existence of Cr ion in the Cr-ZnO. The optical properties and bandgap studies were undertaken by UV–Visible spectroscopy. I-V characterization study was performed to determine the electrical property of ZnO and Cr-ZnO films. - Highlights: • The prism shaped Zn{sub 1−x}Cr{sub x}O (0 ≤ x ≤ 0.15) was prepared by microwave combustion method. • Effect of Cr on the properties of ZnO was reported. • Change in crystal size was explained by lattice strain and Zener-Pinning effect. • The optical measurements shows up to 8 wt% of Cr doping had more efficient. • Compared to ZnO, Cr doped ZnO enhance the photo voltaic activity.

  9. Facile synthesis of TiO2/microcrystalline cellulose nanocomposites: photocatalytically active material under visible light irradiation

    Science.gov (United States)

    Doped TiO2 nanocomposites were prepared in situ by a facile and simple synthesis utilizing benign and renewable precursors such as microcrystalline cellulose (MC) and TiCl4 through hydrolysis in alkaline medium without the addition of organic solvents. The as-prepared nanocompos...

  10. Facile synthesis of improved room temperature gas sensing properties of TiO2 nanostructures: Effect of acid treatment

    CSIR Research Space (South Africa)

    Tshabalala, Zamaswazi P

    2016-03-01

    Full Text Available and Actuators B: Chemical Facile synthesis of improved room temperature gas sensing properties of TiO2 nanostructures: Effect of acid treatment Z.P. Tshabalalaa,b, D.E. Motaunga,∗, G.H. Mhlongoa,∗, O.M. Ntwaeaborwab,∗ a DST/CSIR, National Centre...

  11. Facile room-temperature solution-phase synthesis of a spherical covalent organic framework for high-resolution chromatographic separation.

    Science.gov (United States)

    Yang, Cheng-Xiong; Liu, Chang; Cao, Yi-Meng; Yan, Xiu-Ping

    2015-08-07

    A simple and facile room-temperature solution-phase synthesis was developed to fabricate a spherical covalent organic framework with large surface area, good solvent stability and high thermostability for high-resolution chromatographic separation of diverse important industrial analytes including alkanes, cyclohexane and benzene, α-pinene and β-pinene, and alcohols with high column efficiency and good precision.

  12. Facile synthesis of carbon-ZnO nanocomposite with enhanced visible light photocatalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Akir, Sana [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021, Bizerte (Tunisia); Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopôle de Bordj Cedria, BP73, 8027, Soliman (Tunisia); Hamdi, Abderrahmane [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021, Bizerte (Tunisia); Laboratory of Semi-conductors, Nano-structures and Advanced Technologies, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050, Hammam-Lif (Tunisia); Addad, Ahmed [UMET, UMR CNRS 8207, Université Lille 1, 59655 Villeneuve d' Ascq Cédex (France); Coffinier, Yannick [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Boukherroub, Rabah, E-mail: rabah.boukherroub@iemn.univ-lille1.fr [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); and others

    2017-04-01

    Highlights: • C-ZnO nanocomposite was successfully prepared via a facile and eco-friendly process. • C-ZnO NPs have excellent photocatalytic activity for RhB dye degradation under visible light irradiation compared with literature. • The visible photocatalytic properties originate from injection e{sup −} in CB of ZnO from RhB. - Abstract: The present study describes a facile route for synthesis of carbon-ZnO nanocomposites (C-ZnO) via hydrothermal process in presence of glucose as carbon precursor. The samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) measurements. The results showed carbon uniformly coated on the surface of the ZnO nanoparticles to form the C-ZnO nanocomposites. Further investigation revealed that carbon could significantly protect ZnO NPs against the coalescence during high temperature treatment. The obtained C-ZnO nanocomposite showed excellent photocatalytic activity for the degradation of rhodamine B (RhB) under visible light irradiation, which was attributed to the repressed charge carrier recombination in the nanocomposite. Quenching experiments and photocurrent measurements revealed a photocatalytic mechanism occurring through photosensitization.

  13. The facile and low temperature synthesis of nanophase hydroxyapatite crystals using wet chemistry

    International Nuclear Information System (INIS)

    Dhand, Vivek; Rhee, K.Y.; Park, Soo-Jin

    2014-01-01

    A simple and facile wet chemistry route was used to synthesize nanophase hydroxyapatite (HaP) crystals at low temperature. The synthesis was carried out at a pH of 11.0 and at a temperature of 37 °C. The resulting samples were washed several times and subjected to further analysis. XRD studies revealed that the HaP crystals were polycrystalline in nature with a crystallite size of ∼ 15–60 ± 5 nm. SEM-EDXA images confirmed the presence of calcium (Ca), phosphorous (P), and oxygen (O) peaks. Likewise, FTIR confirmed the presence of characteristic phosphate and hydroxyl peaks in samples. Lastly, HRTEM images clearly showed distinctive lattice fringes positioned in the 100 and 002 planes. TGA analysis shows that HaP crystals can withstand higher calcination temperatures and are thermally stable. - Highlights: • Facile and low temperature nanophase HaP crystals synthesized at pH 11 and 37 °C • Electron microscopy image of HaP shows characteristic rice grain like morphology. • FTIR results show the characteristic and fingerprint functional groups of HaP. • Thermal stability of HaP crystals up to 500 °C • Growth of Hap crystals occur parallel to c-axis and a possible mechanism proposed

  14. Facile Synthesis of Flowerlike LiFe5O8 Microspheres for Electrochemical Supercapacitors.

    Science.gov (United States)

    Lin, Ying; Dong, Jingjing; Dai, Jingjing; Wang, Jingping; Yang, Haibo; Zong, Hanwen

    2017-12-18

    Facile synthesis of porous and hollow spinel materials is very urgent due to their extensive applications in the field of energy storage. In present work, flowerlike porous LiFe 5 O 8 microspheres etched for 15, 30, and 45 min (named as p-LFO-15, p-LFO-30, and p-LFO-45, respectively) are successfully synthesized through a facile chemical etching method based on bulk LiFe 5 O 8 (LFO) particles as precursors, and they are applied as electrode materials for high-performance electrochemical capacitors. In particular, the specific surface area of p-LFO-45 reaches 46.13 m 2 g -1 , which is 112 times greater than that of the unetched counterpart. Therefore, the p-LFO-45 electrode can achieve a higher capacitance of 278 F g -1 at a scan rate of 5 mV s -1 than the unetched counterpart. Furthermore, the p-LFO-45 electrode presents a good cycling stability with 78.3% of capacitive retention after 2000 cycles, which is much higher than that of the unetched LFO particles (66%). Therefore, the flowerlike porous LFO microspheres are very promising candidate materials for supercapacitor applications.

  15. Carbon nanotubes/magnetite hybrids prepared by a facile synthesis process and their magnetic properties

    International Nuclear Information System (INIS)

    Zhang Li; Ni, Qing-Qing; Natsuki, Toshiaki; Fu Yaqin

    2009-01-01

    In this paper, a facile synthesis process is proposed to prepare multiwalled carbon nanotubes/magnetite (MWCNTs/Fe 3 O 4 ) hybrids. The process involves two steps: (1) water-soluble CNTs are synthesized by one-pot modification using potassium persulfate (KPS) as oxidant. (2) Fe 3 O 4 is assembled along the treated CNTs by employing a facile hydrothermal process with the presence of hydrazine hydrate as the mineralizer. The treated CNTs can be easily dispersed in aqueous solvent. Moreover, X-ray photoelectron spectroscopy (XPS) analysis reveals that several functional groups such as potassium carboxylate (-COOK), carbonyl (-C=O) and hydroxyl (-C-OH) groups are formed on the nanotube surfaces. The MWCNTs/Fe 3 O 4 hybrids are characterized with respect to crystal structure, morphology, element composition and magnetic property by X-ray diffraction (XRD), transmission electron microscopy (TEM), XPS and superconducting quantum interference device (SQUID) magnetometer. XRD and TEM results show that the Fe 3 O 4 nanoparticles with diameter in the range of 20-60 nm were firmly assembled on the nanotube surface. The magnetic property investigation indicated that the CNTs/Fe 3 O 4 hybrids exhibit a ferromagnetic behavior and possess a saturation magnetization of 32.2 emu/g. Further investigation indicates that the size of assembled Fe 3 O 4 nanoparticles can be turned by varying experiment factors. Moreover, a probable growth mechanism for the preparation of CNTs/Fe 3 O 4 hybrids was discussed.

  16. Facile synthesis of antimony-doped tin oxide nanoparticles by a polymer-pyrolysis method

    International Nuclear Information System (INIS)

    Li, Yuan-Qing; Wang, Jian-Lei; Fu, Shao-Yun; Mei, Shi-Gang; Zhang, Jian-Min; Yong, Kang

    2010-01-01

    In this article, antimony-doped tin oxide (ATO) nanoparticles was synthesized by a facile polymer-pyrolysis method. The pyrolysis behaviors of the polymer precursors prepared via in situ polymerization of metal salts and acrylic acid were analyzed by simultaneous thermogravimetric and differential scanning calorimetry (TG-DSC). The structural and morphological characteristics of the products were studied by powder X-ray diffraction (XRD) and transmission electron microscope (TEM). The results reveal that the ATO nanoparticles calcined at 600 o C show good crystallinity with the cassiterite structure and cubic-spherical like morphology. The average particle size of ATO decreases from 200 to 15 nm as the Sb doping content increases from 5 mol% to 15 mol%. Electrical resistivity measurement shows that the resistivity for the 10-13 mol% Sb-doped SnO 2 nanoparticles is reduced by more than three orders compared with the pure SnO 2 nanoparticles. In addition, due to its versatility this polymer-pyrolysis method can be extended to facile synthesis of other doped n-type semiconductor, such as In, Ga, Al doped ZnO, Sn doped In 2 O 3 .

  17. Differential behaviour of combustion and gasification fly ash from Puertollano Power Plants (Spain) for the synthesis of zeolites and silica extraction

    International Nuclear Information System (INIS)

    Font, O.; Moreno, N.; Diez, S.; Querol, X.; Lopez-Soler, A.; Coca, P.; Garcia Pena, F.

    2009-01-01

    Coal gasification (IGCC) and pulverised coal combustion (PCC) fly ashes (FAs), obtained from two power plants fed with the carboniferous bituminous coal from Puertollano (Spain), were characterised and used as raw materials for zeolite synthesis by direct conversion (DC) and by alkaline fusion (Fu), and SiO 2 extraction (Si-Ex) at laboratory scale. The Puertollano FAs are characterised by a high SiO 2 content (59%) with respect to EU coal FAs. High zeolite synthesis yields were obtained from both FAs by using conventional alkaline activation. However, the Si extraction yields were very different. The results of the zeolite synthesis from the Si-bearing extracts from both FAs demonstrated that high purity zeolites with high cation exchange capacity (CEC, between 4.3 and 5.3 meq/g) can be produced. The solid residue arising from Si-Ex is also a relatively high NaP1 zeolite product (CEC 2.4-2.7 meq/g) equivalent to the DC products. The zeolitic materials synthesised from both FAs by Fu showed an intermediate (between the high purity zeolites and the DC products) zeolite content with CEC values from 3.4 to 3.7 meq/g. Low leachable metal contents were obtained from high purity A and X zeolites and zeolite material synthesised by Fu for PCC FA.

  18. Processing of hydroxyapatite obtained by combustion synthesis; Procesamiento de hidroxiapatita obtenida mediante síntesis por combustión

    Energy Technology Data Exchange (ETDEWEB)

    Canillas, M.; Rivero, R.; García-Carrodeguas, R.; Barba, F.; Rodríguez, M.A.

    2017-11-01

    One of the reasons of implants failure are the stress forces appearing in the material–tissue interface due to the differences between their mechanical properties. For this reason, similar mechanical properties to the surrounding tissue are desirable. The synthesis of hydroxyapatite by solution combustion method and its processing have been studied in order to obtain fully dense ceramic bodies with improved mechanical strength. Combustion synthesis provides nanostructured powders characterized by a high surface area to facilitate the following sintering. Moreover, synthesis was conducted in aqueous and oxidizing media. Oxidizing media improve homogenization and increase the energy released during combustion. It gives rise to particles whose morphology and size suggest lower surface energies compared with aqueous media. The obtained powders were sintered by using a controlled sintering rate schedule. Lower surfaces energies minimize the shrinkage during sintering and relative densities measurements and diametral compression test confirm improved densification and consequently mechanical properties. [Spanish] Una de las razones principales de fracaso de los implantes son las fuerzas de estrés que aparecen en la interface material-tejido debido a las diferencias existentes entre sus propiedades mecánicas. Por esta razón, es necesario que el implante posea propiedades mecánicas similares a las del tejido circundante. La síntesis de hidroxiapatita por el método de combustión y su procesamiento se han estudiado con el objetivo de obtener cuerpos cerámicos completamente densificados y, consecuentemente, con propiedades mecánicas mejoradas. El método de combustión provee de polvos nanoestructurados que se caracterizan por una superficie específica elevada que facilita el siguiente proceso de sinterización. Además, este proceso de síntesis se ha realizado en medio acuoso y oxidante. El medio oxidante homogeniza e incrementa la energía liberada durante la

  19. High temperature thermoelectric properties of Ca3Co4O9+δ by auto-combustion synthesis and spark plasma sintering

    DEFF Research Database (Denmark)

    Wu, NingYu; Holgate, Tim; Van Nong, Ngo

    2014-01-01

    A rapid method for the synthesis of Ca3Co4O9+δpowder is introduced. The procedure is a modification of the conventional citric-nitrate sol–gelmethod where an auto-combustion process is initiated by a controlled thermal oxidation–reduction reaction. The resulting powders inherit theadvantages...

  20. Storage facilities of spent nuclear fuel in dry for Mexican nuclear facilities; Instalaciones de almacenamiento de combustible nuclear gastado en seco para instalaciones nucleares mexicanas

    Energy Technology Data Exchange (ETDEWEB)

    Salmeron V, J. A.; Camargo C, R.; Nunez C, A.; Mendoza F, J. E.; Sanchez J, J., E-mail: juan.salmeron@cnsns.gob.mx [Comision Nacional de Seguridad Nuclear y Salvaguardias, Dr. Jose Ma. Barragan No. 779, Col. Narvarte, 03020 Mexico D. F. (Mexico)

    2013-10-15

    In this article the relevant aspects of the spent fuel storage and the questions that should be taken in consideration for the possible future facilities of this type in the country are approached. A brief description is proposed about the characteristics of the storage systems in dry, the incorporate regulations to the present Nuclear Regulator Standard, the planning process of an installation, besides the approaches considered once resolved the use of these systems; as the modifications to the system, the authorization periods for the storage, the type of materials to store and the consequent environmental impact to their installation. At the present time the Comision Nacional de Seguridad Nuclear y Salvaguardias (CNSNS) considers the possible generation of two authorization types for these facilities: Specific, directed to establish a new nuclear installation with the authorization of receiving, to transfer and to possess spent fuel and other materials for their storage; and General, focused to those holders that have an operation license of a reactor that allows them the storage of the nuclear fuel and other materials that they possess. Both authorizations should be valued according to the necessities that are presented. In general, this installation type represents a viable solution for the administration of the spent fuel and other materials that require of a temporary solution previous to its final disposal. Its use in the nuclear industry has been increased in the last years demonstrating to be appropriate and feasible without having a significant impact to the health, public safety and the environment. Mexico has two main nuclear facilities, the nuclear power plant of Laguna Verde of the Comision Federal de Electricidad (CFE) and the facilities of the TRIGA Reactor of the Instituto Nacional de Investigaciones Nucleares (ININ) that will require in a future to use this type of disposition installation of the spent fuel and generated wastes. (Author)

  1. Fast solution combustion synthesis of porous NaFeTi3O8 with superior sodium storage properties

    Science.gov (United States)

    Zhao, Jin-Bao; Li, Xue; Xiao, Qian

    2018-01-01

    In this work, NaFeTi3O8 with three-dimensional porous net-like sheet morphology is firstly prepared by a simple and effective solution combustion method. Encouragingly, when being assessed as an anode electrode for sodium ion batteries, the NaFeTi3O8 net-like sheet composite exhibits superior electrochemical properties. We also study the effect of the combustion fuel glycine. The results indicate that the NaFeTi3O8 composite tends to be porous with glycine as the combustion fuel, which displays more excellent long cyclic stability (discharge capacity of 91 mA h g-1 after 1000 cycles at the current density of 0.5 A g-1) and superior rate performance (84.4 mA h g-1 even at 1.6 A g-1) than that of NaFeTi3O8 without glycine as the combustion agent. The enhanced electrochemical properties could be ascribed to the unique porous morphology, which achieves better electrolyte infiltration and faster ion diffusion. [Figure not available: see fulltext.

  2. Self-propagating combustion synthesis of Pb1–x Srx ZrO3 (0≤ x≤ 0 ...

    Indian Academy of Sciences (India)

    Lead strontium zirconate, Pb1–SrZrO3 (0 ≤ ≤ 0.20) ceramics, were prepared by novel glycine–nitrate self-propagating combustion technique. The crystal structure of the ceramics was investigated as a function of composition via X-ray diffraction (XRD). The XRD patterns obtained on these powders showed the ...

  3. Synthesis by the Pechini method and reaction combustion for the preparation of TiO2: a comparative analysis

    International Nuclear Information System (INIS)

    Almeida, E.P.; Ribeiro, P.C.; Freitas, N.L.; Lira, H.L.; Costa, A.C.F.M. da; Kiminami, R.H.G.A.

    2009-01-01

    The aim of this work is to prepare TiO 2 powder by Pechini and combustion reaction methods. A comparative analysis between the structural and morphological results obtained by the two methods was investigated. The powders were characterized by X-ray diffractions (XRD), infrared analysis, nitrogen adsorption (BET) and particle size distribution. The results from XRD show that the powders prepared by Pechini method and by combustion reaction using aniline as fuel, present anatase as major phase and traces of rutile phase. The values of crystallite size and surface area from BET were: 30 e 44 nm; 6.2 e 4.4 m 2 /g, for the powders prepared by Pechini and combustion reaction, respectively. The values of particle size were: 21.9 e 5.3 μm, for the powders prepared by Pechini and combustion reaction, respectively. The Pechini method was more suitable to obtain powders with irregular agglomerates, in the block shape with particles bonded softly and small crystallite size. (author)

  4. Synthesis and photoluminescence properties of CaSixOy:Tb3+ phosphors prepared using solution-combustion method

    CSIR Research Space (South Africa)

    Dejene, FB

    2011-07-01

    Full Text Available Effect of Tb3+ ion concentrations on the structural and persistence luminescence properties of CaSixOy:Tb3+ crystals were evaluated using powders grown by the solution combustion technique. The XRD study indicates the change of phase from CaSiO3...

  5. Thermodynamic calculation and an experimental study of the combustion synthesis of (Mo{sub 1−x}Nb{sub x})Si{sub 2} (0 ⩽ x ⩽ 1)

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiaohong, E-mail: matinbow@163.com; Lu, Qiong; Wu, Guangzhi; Shi, Jialing; Sun, Zhi

    2015-08-25

    Highlights: • (Mo{sub 1−x}Nb{sub x})Si{sub 2} alloys were synthesized by a simple and energy-saving process of SHS. • Theoretical adiabatic temperature of (Mo{sub 1−x}Nb{sub x})Si{sub 2} was calculated for the first time. • The variation of the actual temperature is consistent with theoretical temperature. - Abstract: The theoretical adiabatic temperature of (Mo{sub 1−x}Nb{sub x})Si{sub 2} (0 ⩽ x ⩽ 1) is calculated. The results indicate that the theoretical adiabatic temperature of (Mo{sub 1−x}Nb{sub x})Si{sub 2} increases with an increasing Nb content when (Mo{sub 1−x}Nb{sub x})Si{sub 2} is of a single-phase structure, but decreases with an increasing Nb content when (Mo{sub 1−x}Nb{sub x})Si{sub 2} is of a double-phase structure. All of the temperatures are higher than 1800 K, indicating that (Mo{sub 1−x}Nb{sub x})Si{sub 2} (0 ⩽ x ⩽ 1) can be prepared by the combustion synthesis method. In this work, (Mo{sub 1−x}Nb{sub x})Si{sub 2} (0 ⩽ x ⩽ 1) alloys are successfully synthesized by the combustion synthesis process from elemental powders of Mo, Nb, and Si. The highest combustion temperature and combustion product structure are studied. The results confirm that the variation of the experimental maximum combustion temperature of (Mo{sub 1−x}Nb{sub x})Si{sub 2} is consistent with that of the theoretical adiabatic temperature. The combustion products are non-equilibrium species, and a supersaturated solid solution of C11{sub b} type (Mo{sub 1−x}Nb{sub x})Si{sub 2} forms during combustion synthesis.

  6. Luminescence properties of ZnMoO{sub 4}:Eu{sup 3+}:Y{sup 3+} materials synthesized by solution combustion synthesis method

    Energy Technology Data Exchange (ETDEWEB)

    Verma, Naveen, E-mail: vermanaveen17@gmail.com; Singh, Krishan Chander; Jindal, Jitender; Yadav, Suprabha [Department of chemistry, Maharshi Dayanand University, Rohtak-124001 – India (India); Mari, Bernabe; Mollar, Miguel [Institut de Disseny per la Fabricació Automatitzada - Departament de Física Aplicada, Universitat Politècnica de València, Camí de Vera s/n, 46022 València (Spain)

    2016-04-13

    The Zn{sub (1-x-y)}MoO{sub 4}:Eu{sup 3+}{sub (x)}: Y{sup 3+}{sub (y)} (x = 1 mol% and y = 1 or 2 mol%) compounds were prepared by combustion synthesis method. The crystal structure of the samples was identified by X-ray diffraction (XRD). The photoluminescence properties were investigated and it is observed that the co-doping of Y{sup 3+} enhances the luminescence emission intensity of ZnMoO{sub 4}:Eu{sup 3+} material. The Y{sup 3+} acts as a sensitizer in the ZnMoO{sub 4}:Eu{sup 3+} lattice. The particle size is calculated from XRD data by using Scherer Equation. The particles has been found in the range of 30-40 nm.

  7. Sintering evaluation of spinel MA nanostructured obtained via synthesis of combustion in solution; Avaliacao da sinterizacao de espinelio MA nanoestruturado obtido via combustao em solucao

    Energy Technology Data Exchange (ETDEWEB)

    Vitor, P.A.M.; Braganca, S.R.; Bergmann, C.P., E-mail: pedroaugusto89@hotmail.com [Universidade Federal do Rio Grande do Sul (LACER/UFRGS), Porto Alegre, RS (Brazil). Laboratorio de Materiais Ceramicos

    2016-07-01

    Specimens were shaped from powders of spinel MA (MgAl2O4) obtained via synthesis combustion in solution (SCS) from the trio chemical precursor aluminum nitrate, magnesium nitrate and sucrose in water, and then sintered at different temperatures between 1350 and 1650 ° C. Were evaluated the physical properties (density, porosity, water absorption and linear shrinkage), mechanical (flexural 4 points), and the microstructures (SEM) as a function of sintering temperature. The densification increased with growing the value of the sintering temperature, wherein the temperature to 1650 ° C had the highest flexural strength and higher elastic modulus: 51.33 (± 6.83) and 26.16 MPa (± 5.06) GPa respectively. The study confirmed the microstructure of the densification of the particles, confirming the purity and nature of nanometric powders obtained via the SCS. (author)

  8. Synthesis NiAl1,0Fe1,0O4 catalyst by the combustion reaction to their use in the shift reaction (WGSR)

    International Nuclear Information System (INIS)

    Santos, P.T.A.; Costa, A.C.F.M.; Neiva, L.S.; Gama, L.; Argolo, F.; Andrade, H.M.C.

    2009-01-01

    This work aims at the synthesis of catalyst NiAl 1,0 Fe 1,0 O 4 by combustion reaction using urea as fuel, to evaluate its performance in the production of hydrogen by the reaction of displacement of water vapor (WGSR). The initial composition of the solution was based on valencia total oxidizing and reducing reagents based on the concepts of the chemistry of propellants, using container as a crucible of glassy silica. The resulting powder was characterized by X-ray diffraction, infrared spectroscopy, nitrogen adsorption isotherms (BET), scanning electronic microscope and catalytic tests. The DRX results reveal the presents majoritary phase NiAl 1,0 Fe 1,0 O 4 spinel, the catalyst presents surface area 28 m 2 /g and isotherms type III. Higher conversion CO/CO 2 of 75% CO conversion observed at 500 deg C and catalytic activity of 43 mmolg -1 .h -1 at 450 deg C. (author)

  9. Study of photoluminescence properties of CaAl{sub 2}O{sub 4}: Eu{sup 2+} prepared by combustion synthesis method

    Energy Technology Data Exchange (ETDEWEB)

    Hingwe, V. S., E-mail: vishwas.hingwe@yahoo.in; Omanwar, S. K. [Department of physics, SGB Amravati University Amravati-444602 (India); Bajaj, N. S. [Toshniwal Arts, Commerce and Science College Sengaon-431542 (India)

    2016-05-06

    Eu{sup 2+} doped alkaline earth metals such as strontium aluminate, calcium aluminate and barium aluminate prepared by using modified combustion synthesis method at 600°C with Urea as fuel. Crystal structure is determined by using XRD and the sample confirmation by using the FTIR. The effect of the host material on the photoluminescence (PL) and phosphorescence properties were studied by using the Hitachi F-7000 spectrofluorimeter equipped with a 450W Xenon lamp, in the range 200-650 nm. The emission spectra of Eu{sup 2+} range from 450 to 500 nm in the Blue to aqua region and the transition 4f{sup 7}-4f{sup 6} 5d{sup 1}. The observed emission in CaAl{sub 2}O{sub 4} is 440 nm.

  10. Facile high-yield synthesis of polyaniline nanosticks with intrinsic stability and electrical conductivity.

    Science.gov (United States)

    Li, Xin-Gui; Li, Ang; Huang, Mei-Rong

    2008-01-01

    Chemical oxidative polymerization at 15 degrees C was used for the simple and productive synthesis of polyaniline (PAN) nanosticks. The effect of polymerization media on the yield, size, stability, and electrical conductivity of the PAN nanosticks was studied by changing the concentration and nature of the acid medium and oxidant and by introducing organic solvent. Molecular and supramolecular structure, size, and size distribution of the PAN nanosticks were characterized by UV/Vis and IR spectroscopy, X-ray diffraction, laser particle-size analysis, and transmission electron microscopy. Introduction of organic solvent is advantageous for enhancing the yield of PAN nanosticks but disadvantageous for formation of PAN nanosticks with small size and high conductivity. The concentration and nature of the acid medium have a major influence on the polymerization yield and conductivity of the nanosized PAN. The average diameter and length of PAN nanosticks produced with 2 M HNO(3) and 0.5 M H(2)SO(4) as acid media are about 40 and 300 nm, respectively. The PAN nanosticks obtained in an optimal medium (i.e., 2 M HNO(3)) exhibit the highest conductivity of 2.23 S cm(-1) and the highest yield of 80.7 %. A mechanism of formation of nanosticks instead of nanoparticles is proposed. Nanocomposite films of the PAN nanosticks with poly(vinyl alcohol) show a low percolation threshold of 0.2 wt %, at which the film retains almost the same transparency and strength as pure poly(vinyl alcohol) but 262 000 times the conductivity of pure poly(vinyl alcohol) film. The present synthesis of PAN nanosticks requires no external stabilizer and provides a facile and direct route for fabrication of PAN nanosticks with high yield, controllable size, intrinsic self-stability, strong redispersibility, high purity, and optimizable conductivity.

  11. Assessment of the synthesis conditions for nano-Bi{sub 4}Ti{sub 3}O{sub 12} production by the combustion route; Avaliacao das condicoes de sintese para producao de nano-Bi{sub 4}Ti{sub 3}O{sub 12} pelo metodo de combustao

    Energy Technology Data Exchange (ETDEWEB)

    Dias, Jeferson A.; Nascimento, Cassia C.; Oliveira, Jessica A.; Morelli, Marcio R., E-mail: jeferson.unifal@gmail.com [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil)

    2016-07-01

    The bismuth titanate has interesting optoelectronic properties. Its production in nanometric scale is important due to the demand of miniaturized electronic devices and greater synthesization facility. This study aims at the evaluation of synthesis parameters for nano-Bi{sub 4}Ti{sub 3}O{sub 12} production by the combustion route. For that, the materials were synthesized and calcined at 600°C, 700°C and 800°C. The materials were posteriorly characterized by X-Ray diffraction, SEM, DSC-TGA, FTIR; DRS and impedance spectroscopy. The results have demonstrated that the combustion method was effective for nanocrystalline powders production, which also showed high levels of purity. Particles size growth was observed for high treatment temperatures. Low level of residual organic matter was determined and the high electrical resistivity was observed. The temperature of 600°C was enough to produce particles with optimal properties. Therefore, the results have confirmed the efficacy of combustion route to produce nanometric Bi{sub 4}Ti{sub 3}O{sub 12}. (author)

  12. Synthesis, characterisation, luminescence and defect centres in solution combustion synthesised CaZrO{sub 3}:Tb{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Vijay, E-mail: vijayjiin2006@yahoo.com [School of Information and Communications, Gwangju Institute of Science and Technology, Gwangju 500-712 (Korea, Republic of); Watanabe, S.; Gundu Rao, T.K. [Institute of Physics, University of Sao Paulo, 05508-090 Sao Paulo/SP (Brazil); Al-Shamery, Katharina [Physical Chemistry, Institute for Pure and Applied Chemistry and Center of Interface Science University of Oldenburg, 26129 Oldenburg (Germany); Haase, Markus [Department of Inorganic Chemistry I-Materials Research, Institute of Chemistry, University of Osnabrueck, Barbarastrabe 7, 49069 Osnabrueck (Germany); Jho, Young-Dahl, E-mail: jho@gist.ac.kr [School of Information and Communications, Gwangju Institute of Science and Technology, Gwangju 500-712 (Korea, Republic of)

    2012-08-15

    Tb{sup 3+} doped CaZrO{sub 3} has been prepared by an easy solution combustion synthesis method. The combustion derived powder was investigated by X-ray diffraction, Fourier-transform infrared spectrometry and scanning electron microscopy techniques. A room temperature photoluminescence study showed that the phosphors can be efficiently excited by 251 nm light with a weak emission in the blue and orange region and a strong emission in green light region. CaZrO{sub 3}:Tb{sup 3+} exhibits three thermoluminescence (TL) glow peaks at 126 Degree-Sign C, 200 Degree-Sign C and 480 Degree-Sign C. Electron Spin Resonance (ESR) studies were carried out to study the defect centres induced in the phosphor by gamma irradiation and also to identify the centres responsible for the TL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0233 is identified as an O{sup -} ion. Centre II with an axial symmetric g-tensor with principal values g{sub Up-Tack }=1.9986 and g{sub Up-Tack }=2.0023 is assigned to an F{sup +} centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal annealing experiments and this centre (assigned to F{sup +} centre) seems to originate from an F centre (oxygen vacancy with two electrons). The F centre and also the F{sup +} centre appear to correlate with the observed high temperature TL peak in CaZrO{sub 3}:Tb{sup 3+} phosphor. - Highlights: Black-Right-Pointing-Pointer Powder phosphor of CaZrO{sub 3}:Tb{sup 3+} was prepared by an easy solution combustion synthesis method. Black-Right-Pointing-Pointer The phosphor exhibits a bright green emission at 545 nm ({sup 5}D{sub 4}{yields}{sup 7}F{sub 5}) of the Tb{sup 3+} ion. Black-Right-Pointing-Pointer Electron Spin Resonance studies have been carried out to identify the defect centres responsible for the observed thermoluminescence peaks.

  13. Facile synthesis of PdAgTe nanowires with superior electrocatalytic activity

    Science.gov (United States)

    Hong, Wei; Wang, Jin; Wang, Erkang

    2014-12-01

    In this work, ultrathin Te nanowires (NWs) with high-aspect-ratio are prepared by a simple hydrothermal method. By using Te NWs as the sacrificial template, we demonstrate a facile and efficient method for the synthesis of PdAgTe NWs with high-quality through the partly galvanic replacement between Te NWs and the corresponding noble metal salts precursors in an aqueous solution. The compositions of PdAgTe NWs can be tuned by simply altering the concentration of the precursors. After cyclic voltammetry treatment, multi-component PdAgTe NW with a highly active and stable surface can be obtained. The structure and composition of the as-prepared nanomaterials are analyzed by transmission electron microscope, X-ray diffraction, energy dispersive X-ray spectroscopy, inductively coupled plasma-mass spectroscopy and X-ray photoelectron spectroscopy. Electrochemical catalytic measurement results prove that the as synthesized PdAgTe NWs present superior catalytic activity toward ethanol electrooxidation in alkaline solution than the commercial Pd/C catalyst, which making them can be used as effective catalysts for the direct ethanol fuel cells.

  14. Facile synthesis of indole-pyrimidine hybrids and evaluation of their anticancer and antimicrobial activity

    Directory of Open Access Journals (Sweden)

    Nikhila Gokhale

    2017-11-01

    Full Text Available The paper describes the facile synthesis of new N-cyclopropyl-1-methyl-1H-indole-2-carboxamide derivatives bearing substituted 2-amino pyrimidine moiety at position-3 of the indole ring. All the intermediate and title compounds were characterized adeptly by 1H NMR, 13C NMR, ESI–MS and elemental analyses. These compounds were evaluated for their in vitro anticancer activity against HeLa, HepG2 and MCF-7 cells. Three among 22 molecules, showed more than 70% growth inhibition against all three tested cancer cells. The nature of the substituent group on the pyrimidine ring (R2 affected significantly the anti-proliferative activity of the molecules. The anti-microbial evaluation of the title molecules revealed the significance of fluoro/chloro groups (R2 in enhancing their inhibition activity. Eight molecules which contain fluoro/chloro groups showed potent anti-microbial activity. In addition, the active molecules displayed negligible toxicity to benign Vero cells.

  15. Facile synthesis of cyclopentenone B1- and L1-type Phytoprostanes

    Directory of Open Access Journals (Sweden)

    Alexandre eGuy

    2015-07-01

    Full Text Available Phytoprostanes (PhytoPs represent non-enzymatic metabolites of α-linolenic acid (ALA, the essential omega-3 polyunsaturated fatty acid (PUFA derived from plants. PhytoPs are present in the plant kingdom and represent endogenous mediators capable of protecting cells from oxidative stress damages in plants. Recently, it was found that such metabolites are present in cooking oil in high quantities, and also that B1-PhytoPs protect immature neurons from oxidant injury and promote differentiation of oligodendrocyte progenitors through PPAR-γ activation. We report a novel and facile synthesis of natural 2,3-substituted cyclopentenone PhytoPs, 16-B1-PhytoP and 9-L1-PhytoP. Our strategy is based on reductive alkylation at the 2-position of 1,3-cyclopentanedione using a recent protocol developed by Ramachary et al., and on a cross-coupling metathesis to access conjugate dienone system. In conclusion, this strategy permitted access to B1- and L1-PhytoPs in a relative short sequence process, and afford the possibility to easily develop analogs of PhytoPs.

  16. Facile synthesis and antimicrobial evaluation of some new heterocyclic compounds incorporating a biologically active sulfamoyl moiety.

    Science.gov (United States)

    Darwish, Elham S

    2014-01-01

    A facile and convenient synthesis of new heterocyclic compounds containing a sulfamoyl moiety suitable for use as antimicrobial agents was reported. The precursor 3-oxo-3-phenyl-N-(4-sulfamoylphenyl)propionamide was coupled smoothly with arenediazonium salt producing hydrazones which reacted with malononitrile or triethylorthoformate affording pyridazine and triazine derivatives, respectively. Also, the reactivity of the same precursor with DMF-DMA was followed by aminotriazole; aromatic aldehydes was followed by hydrazine hydrate, triethylorthoformate, or thiourea affording triazolo[1,5-a]pyrimidine, pyrazole, acrylamide, and dihydropyrimidine derivatives, respectively. On the other hand, treatment of the precursor propionamide with phenyl isothiocyanate and KOH in DMF afforded the intermediate salt which was treated with dilute HCl followed by 2-bromo-1-phenylethanone affording carboxamide derivative. While the same intermediate salt reacted in situ with chloroacetone, ethyl 2-chloroacetate, 3-(2-bromoacetyl)-2H-chromen-2-one, methyl iodide, or 2-oxo-N-phenylpropane hydrazonoyl chloride afforded the thiophene, ketene N,S-acetal, and thiadiazole derivatives, respectively. The structure of the new products was established based on elemental and spectral analysis. Antimicrobial evaluation of some selected examples from the synthesized products was carried out whereby four compounds were found to have moderate activities and one compound showed the highest activity.

  17. Facile and rapid synthesis of nickel nanowires and their magnetic properties

    International Nuclear Information System (INIS)

    Tang Shaochun; Zheng Zhou; Vongehr, Sascha; Meng Xiangkang

    2011-01-01

    The present work reports a facile and rapid microwave-assisted route to synthesize nickel nanowires with a necklace-like morphology and lengths up to several hundreds of microns. The wires consist of many crystallites with an average size of 25 ± 2 nm. The synthesis does not use templates or magnetic fields and needs only 6 min, which is more than 480 times faster than that needed for Ni wires prepared at 180 °C using conventional heating. Nickel nanostructures with various morphologies including spheres, chains and irregular particles with porous surfaces can also be obtained by adjusting reaction parameters. Polyvinylpyrrolidone (PVP) is found to be vital for the formation of the one-dimensional chains and a high concentration of PVP smoothes their surfaces to result in the appearance of wires. This rapid one-pot procedure combines the formation of nanoparticles, their oriented assembly into chains, and the subsequent shaping of wires. The Ni nanostructures show variable magnetic properties. The prepared nickel wires have a high mechanical stability and exhibit much higher coercivity than bulk nickel, Ni nanoparticles and their aggregations, which promise potential applications in micromechanical sensors, memory devices and other fields.

  18. Facile synthesis and electron transport properties of NiO nanostructures investigated by scanning tunneling microscopy

    Directory of Open Access Journals (Sweden)

    Govind Mallick

    2017-08-01

    Full Text Available Due to their unique chemical, thermal, electronic and photonic properties, low -dimensional transition metal oxides, especially NiO, have attracted great deal of attention for potential applications in a wide range of technologies, such as, sensors, electrochromic coatings and self-healing materials. However, their synthesis involves multi-step complex procedures that in addition to being expensive, further introduce impurities. Here we present a low cost facile approach to synthesize uniform size NiO nanoparticles (NPs from hydrothermally grown Ni(OH2. Detailed transmission electron microscopic analysis reveal the average size of NiO NPs to be around 29 nm. The dimension of NiO NP is also corroborated by the small area scanning tunneling microscope (STM measurements. Further, we investigate electron transport characteristics of newly synthesized Ni(OH2 and NiO nanoparticles on p-type Si substrate using scanning tunneling microscopy. The conductivity of Ni(OH2 and NiO are determined to be 1.46x10-3 S/cm and 2.37x10-5 S/cm, respectively. The NiO NPs exhibit a lower voltage window (∼0.7 V electron tunneling than the parent Ni(OH2.

  19. Facile Synthesis Polyethylene Glycol Coated Magnetite Nanoparticles for High Colloidal Stability

    Directory of Open Access Journals (Sweden)

    Mun Foong Tai

    2016-01-01

    Full Text Available Polyethylene glycol (PEG is one of the most frequently used synthetic polymers for surface modifications of magnetite nanoparticles (MNPs to provide a new opportunity for constructing high colloidal stability. Herein, a facile in situ coprecipitation technique is described for the synthesis of PEG coated MNPs using ammonium hydroxide as the precipitating agent. The structure and morphology of the prepared PEG coated MNPs samples were characterized by Fourier transform infrared (FTIR spectroscopy, X-ray spectroscopy, thermogravimetric analysis (TGA, and the high resolution transmission electron microscopy (HRTEM. In this study, all samples demonstrated hydrodynamic size in the range of 32 to 43 nm with narrow size distribution. In addition, the magnetic properties of resultant samples were investigated using a vibrating sample magnetometer (VSM to reveal the superparamagnetic behaviour with saturation magnetization. The saturation magnetization of PEG coated MNPs samples was in the range of 63 to 66 emu/g at 300 K. Interestingly, it was found that 1.0 g of PEG coated MNPs exhibited high colloidal stability in a basic solution (pH = 10 and nitrile (NBR latex up to 21 days as compared to the unmodified MNPs during the sedimentation test.

  20. Stacking faults enriched silver nanowires: facile synthesis, catalysis and SERS investigations.

    Science.gov (United States)

    Xu, Minmin; Yang, Fengzhu; Yuan, Yaxian; Guo, Qinghua; Ren, Bin; Yao, Jianlin; Gu, Renao

    2013-10-01

    A facile approach based on seed-mediated method for synthesis of stacking faults enriched Ag nanowires (SFEANWs) was successfully developed. SFEANWs were formed and attached onto the seed (α-Fe2O3/Au) surfaces through the reduction of AgNO3 by ascorbic acid (AA) in the presence of sodium polyacrylate (PAANa). Their length can be tuned with different concentrations of AgNO3 or PAANa. According to the effects of seeds and PAANa, the plausible growth mechanism of SFEANWs was discussed. The catalytic activity of SFEANWs comparing with fivefold twinned Ag nanowires (FFTANWs) was evaluated through reducing p-nitrophenol by NaBH4. The activation energy of the classical reaction catalyzed by SFEANWs was calculated through the Arrhenius equation. In addition, these SFEANWs exhibited excellent surface enhanced Raman scattering (SERS) activities due to the hot spots located in the cross of the twist wires. The detection limit of by SERS for 1,4-benzenedithiol (1,4-BDT) was estimated about 10(-7) mol/L. Copyright © 2013 Elsevier Inc. All rights reserved.

  1. Facile Synthesis of ZnO Nanoparticles and Their Photocatalytic Activity

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jun Young; Ko, Sung Hyun; Kim, Sang Wook [Dongguk Univ., Yongin (Korea, Republic of); Lee, Sookeun; Kim, A Young [Daegu Gyeongbuk Institute of Science and Technology, Daegu (Korea, Republic of)

    2014-07-15

    This paper reports the facile synthesis methods of zinc oxide (ZnO) nanoparticles, using diethylene glycol (DEG) and polyethylene glycol (PEG400). The particle size and morphology were correlated with the PEG concentration and reaction time. With 0.75 mL of PEG400 in 150 mL of DEG and a 20 h reaction time, the ZnO nanoparticles began to disperse from a collective spherical grain shape. The ZnO nanoparticles were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and a N{sub 2} adsorption.desorption studies. The Brunauer-Emmett-Teller (BET) surface areas of and were 157.083, 141.559 and 233.249 m{sup 2}/g, respectively. The observed pore diameters of and were 63.4, 42.0 and 134.0 A, respectively. The pore volumes of and were 0.249, 0.148 and 0.781 cm{sup 3}/g, respectively. The photocatalytic activity of the synthesized ZnO nanoparticles was evaluated by methylene blue (MB) degradation, and the activity showed a good correlation with the N{sub 2} adsorption.desorption data.

  2. Facile and sustainable synthesis of shaped iron oxide nanoparticles: effect of iron precursor salts on the shapes of iron oxides.

    Science.gov (United States)

    Sayed, Farheen N; Polshettiwar, Vivek

    2015-05-05

    A facile and sustainable protocol for synthesis of six different shaped iron oxides is developed. Notably, all the six shapes of iron oxides can be synthesised using exactly same synthetic protocol, by simply changing the precursor iron salts. Several of the synthesised shapes are not reported before. This novel protocol is relatively easy to implement and could contribute to overcome the challenge of obtaining various shaped iron oxides in economical and sustainable manner.

  3. Facile combustion based engineering of novel white light emitting Zn2TiO4:Dy3+ nanophosphors for display and forensic applications

    Directory of Open Access Journals (Sweden)

    K.M. Girish

    2017-09-01

    Full Text Available Nanomaterials find a wide range of applications in surface based nanoscience and technology. To pass high backward encumbrance, low sensitivity, complicated setup and poor universality in traditional methods for the enhancement of latent fingerprints and display applications, we explored the superstructures of dysprosium (Dy3+ doped Zn2TiO4 via a facile solution combustion route. This method offers new potentials in surface-based science comprising display, latent fingerprint, and luminescent ink for anticounterfeiting applications. The characteristic emissions of intra-4f shell Dy3+ cations in blue, yellow and red regions corresponding to 4F9/2 to 6H15/2, 6H13/2, and 6H11/2 transitions respectively, showed white emission, and the Judd–Ofelt theory was used to estimate photometric parameters. The concentration quenching phenomenon is discussed based on possible interactions. Our study reveals a new prospect of using optimized Zn2TiO4:Dy3+ nanophosphors for research in display, fingerprint detection, cheiloscopy, anti-counterfeiting technology, ceramic pigment and forensic applications.

  4. Sandia Combustion Research Program

    Energy Technology Data Exchange (ETDEWEB)

    Johnston, S.C.; Palmer, R.E.; Montana, C.A. (eds.)

    1988-01-01

    During the late 1970s, in response to a national energy crisis, Sandia proposed to the US Department of Energy (DOE) a new, ambitious program in combustion research. Shortly thereafter, the Combustion Research Facility (CRF) was established at Sandia's Livermore location. Designated a ''user facility,'' the charter of the CRF was to develop and maintain special-purpose resources to support a nationwide initiative-involving US inventories, industry, and national laboratories--to improve our understanding and control of combustion. This report includes descriptions several research projects which have been simulated by working groups and involve the on-site participation of industry scientists. DOE's Industry Technology Fellowship program, supported through the Office of Energy Research, has been instrumental in the success of some of these joint efforts. The remainder of this report presents results of calendar year 1988, separated thematically into eleven categories. Referred journal articles appearing in print during 1988 and selected other publications are included at the end of Section 11. Our traditional'' research activities--combustion chemistry, reacting flows, diagnostics, engine and coal combustion--have been supplemented by a new effort aimed at understanding combustion-related issues in the management of toxic and hazardous materials.

  5. Combustion synthesis and photoluminescence properties of LaAlO{sub 3} nanophosphors doped with Yb{sup 3+} ions

    Energy Technology Data Exchange (ETDEWEB)

    Dhahri, A. [Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopole de Borj Cedria, B.P. 73, Soliman 8027 (Tunisia); Horchani-Naifer, K., E-mail: karima_horchani@yahoo.com [Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopole de Borj Cedria, B.P. 73, Soliman 8027 (Tunisia); Benedetti, A. [Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca’ Foscari Venezia, Dorsoduro 2137, 30123 Venezia (Italy); Enrichi, F. [CIVEN – Coordinamento Interuniversitario Veneto per le Nanotecnologie, Via Delle Industrie 5, Marghera, Venice 30175 (Italy); Ferid, M. [Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopole de Borj Cedria, B.P. 73, Soliman 8027 (Tunisia)

    2014-09-15

    Ytterbium doped lanthanum aluminate (LaAlO{sub 3}) nanophosphors have been prepared by a combustion process with glycine as a fuel. The structures of the powders were determined by X-ray diffraction (XRD), the morphology of the annealed materials was observed using scanning electron microscopy (SEM), the average crystalline grain sizes have been determined by transmission electron microscopy (TEM) and photoluminescence properties using fluorescence spectroscopy. Pure LaAlO{sub 3} phase was obtained at 800 °C heated for 4 h, with an average crystal size, as determined by TEM, of 60 nm. Emission spectra and decay times of main luminescence transitions were measured at room temperature. A strong emission is reported at 986 nm from the ({sup 2}F{sub 5/2}→{sup 2}F{sub 7/2}) transition, whose intensity depends on Yb concentration. - Highlights: • Ytterbium doped lanthanum aluminate (LaAlO{sub 3}) nanophosphors have been prepared by a combustion process with glycine as a fuel. • Powders were characterized by DRX, FTIR, TEM and fluorescence spectroscopy. • Pure LaAlO{sub 3} phase was obtained at 800 °C heated for 4 h, with an average crystal size of 60 nm. • A strong emission is reported at 986 nm from the ({sup 2}F{sub 5/2}→{sup 2}F{sub 7/2}) transition, whose intensity depends on Yb concentration.

  6. Gel-combustion synthesis of CoSb2O6 and its reduction to powdery Sb2Co alloy

    Directory of Open Access Journals (Sweden)

    MAJA JOVIC

    2009-01-01

    Full Text Available Sb2Co alloy in powdery form was synthesized via reduction with gaseous hydrogen of the oxide CoSb2O6, obtained by the citrate gel-combustion technique. The precursor was an aqueous solution of antimony nitrate, cobalt nitrate and citric acid. The precursor solution with mole ratio Co(II/Sb(V of 1:2 was gelatinized by evaporation of water. The gel was heated in air up to the temperature of self-ignition. The product of gel combustion was a mixture of oxides and it had to be additionally thermally treated in order to be converted to pure CoSb2O6. The reduction of CoSb2O6 by gaseous hydrogen yielded powdery Sb2Co as the sole phase. The process of oxide reduction to alloy was controlled by thermogravimetry, while X-ray diffractometry was used to control the phase compositions of both the oxides and alloys.

  7. Air Emissions Sampling from Vacuum Thermal Desorption for Mixed Wastes Designated with a Combustion Treatment Code for the Energy Solutions LLC Mixed Waste Facility

    International Nuclear Information System (INIS)

    Christensen, M.E.; Willoughby, O.H.

    2009-01-01

    EnergySolutions LLC is permitted by the State of Utah to treat organically-contaminated Mixed Waste by a vacuum thermal desorption (VTD) treatment process at its Clive, Utah treatment, storage, and disposal facility. The VTD process separates organics from organically-contaminated waste by heating the material in an inert atmosphere, and captures them as concentrated liquid by condensation. The majority of the radioactive materials present in the feed to the VTD are retained with the treated solids; the recovered aqueous and organic condensates are not radioactive. This is generally true when the radioactivity is present in solid form such as inorganic salts, metals or metallic oxides. The exception is when volatile radioactive materials are present such as radon gas, tritium, or carbon-14 organic chemicals. Volatile radioactive materials are a small fraction of the feed material. On August 28, 2006, EnergySolutions submitted a request to the USEPA for a variance to the Land Disposal Restrictions (LDR) standards for wastes designated with the combustion treatment code (CMBST). The final rule granting a site specific treatment variance was effective June 13, 2008. This variance is an alternative treatment standard to treatment by CMBST required for these wastes under USEPA's rules. The State of Utah provides oversight of the VTD processing operations. A demonstration test for treating CMBST-coded wastes was performed on April 29, 2008 through May 1, 2008. Three separate process cycles were conducted during this test. Both solid/liquid samples and emission samples were collected each day during the demonstration test. To adequately challenge the unit, feed material was spiked with trichloroethylene, o-cresol, dibenzofuran, and coal tar. Emission testing was conducted by EnergySolutions' emissions test contractor and sampling for radioactivity within the off-gas was completed by EnergySolutions' Health Physics department. This report discusses the emission testing

  8. Nanoscale semiconductor-insulator-metal core/shell heterostructures: facile synthesis and light emission

    Science.gov (United States)

    Li, Gong Ping; Chen, Rui; Guo, Dong Lai; Wong, Lai Mun; Wang, Shi Jie; Sun, Han Dong; Wu, Tom

    2011-08-01

    Controllably constructing hierarchical nanostructures with distinct components and designed architectures is an important theme of research in nanoscience, entailing novel but reliable approaches of bottom-up synthesis. Here, we report a facile method to reproducibly create semiconductor-insulator-metal core/shell nanostructures, which involves first coating uniform MgO shells onto metal oxide nanostructures in solution and then decorating them with Au nanoparticles. The semiconductor nanowire core can be almost any material and, herein, ZnO, SnO2 and In2O3 are used as examples. We also show that linear chains of short ZnO nanorods embedded in MgO nanotubes and porous MgO nanotubes can be obtained by taking advantage of the reduced thermal stability of the ZnO core. Furthermore, after MgO shell-coating and the appropriate annealing treatment, the intensity of the ZnO near-band-edge UV emission becomes much stronger, showing a 25-fold enhancement. The intensity ratio of the UV/visible emission can be increased further by decorating the surface of the ZnO/MgO nanowires with high-density plasmonic Au nanoparticles. These heterostructured semiconductor-insulator-metal nanowires with tailored morphologies and enhanced functionalities have great potential for use as nanoscale building blocks in photonic and electronic applications.Controllably constructing hierarchical nanostructures with distinct components and designed architectures is an important theme of research in nanoscience, entailing novel but reliable approaches of bottom-up synthesis. Here, we report a facile method to reproducibly create semiconductor-insulator-metal core/shell nanostructures, which involves first coating uniform MgO shells onto metal oxide nanostructures in solution and then decorating them with Au nanoparticles. The semiconductor nanowire core can be almost any material and, herein, ZnO, SnO2 and In2O3 are used as examples. We also show that linear chains of short ZnO nanorods embedded in

  9. Facile synthesis, dielectric properties and electrocatalytic activities of PMMA-NiFe2O4 nanocomposite

    International Nuclear Information System (INIS)

    Maji, Pranabi; Choudhary, Ram Bilash

    2017-01-01

    The paper deals with the dielectric and catalytic properties of poly (methyl methacrylate)-nikel ferrite (PMMA-NiFe 2 O 4 ) nanocomposite. The nanocomposite was prepared by using a general and facile synthesis strategy. Fourier transform infrared (FTIR) and X-ray diffraction (XRD) spectra confirmed the formation of PMMA-NiFe 2 O 4 nanocomposite. Field effect scanning electron microscopic (FESEM) and transmission electron microscopic (TEM) images revealed that NiFe 2 O 4 nanoparticles were uniformly distributed and were tightly adhered with PMMA matrix owing to surface modification with 3-methacryloyloxy propyl trimethoxy silane (KH-570). Thermal stability was enhanced by incorporation of NiFe 2 O 4 nanofillers. The nanocomposite showed high dielectric constant and low dielectric loss. The achieved dielectric and thermal property inferred the potential application of this material in energy storage and embedded electronics devices. Further, the as prepared nanocomposite also offered a remarkable electrochemical performance towards hydrogen peroxide (H 2 O 2 ) sensing. - Highlights: • PMMA-NiFe 2 O 4 nanocomposite was synthesized via free radical polymerization. • The nanocomposite exhibited high value of dielectric constant (51) and tanδ (0.3). • Thermal stability of the PMMA matrix was improved by the incorporation of NiFe 2 O 4. • The H 2 O 2 detection limit was estimated 44 μM when signal to noise (S/N) ration was 3. • The electrochemical sensitivity of H 2 O 2 was calculated 0.6727 μA mM -1 .

  10. Facile synthesis of carbon/MoO 3 nanocomposites as stable battery anodes

    KAUST Repository

    Ding, Jiang

    2017-03-09

    Pristine MoO3 is a potential anode material for lithium-ion batteries (LIBs), due to its high specific capacity (1117 mA h g−1); it suffers, however, from poor cyclability, resulting from a low conductivity and large volume changes during lithiation/delithiation process. Here we adopt a facile two-step method in which pristine bulk MoO3 is first converted into MoO3 nanorods (MoO3 NR) through mechanical grinding, to buffer the continuous volume changes, and then coated with amorphous carbon through simple stirring and heating, to provide high electronic and ionic conductivities. Electrochemical tests reveal that the carbon-coated MoO3 nanorods (C-MoO3 NRs) exhibit outstanding specific capacity (856 mA h g−1 after 110 cycles at a current density of 0.1 C); remarkable cycle life, among the best reported for carbon-based MoO3 nanostructures (485 mA h g−1 after 300 cycles at 0.5 C and 373 mA h g−1 after 400 cycles at 0.75 C); and greatly improved capacity retention (up to 90.4% after various C-rates) compared to bulk MoO3. We confirm the versatility of the C-MoO3 NR anodes by preparing flexible batteries that display stable performance, even in bent state. This simple approach toward C-MoO3 NR anodes proceeds without rigorous chemical synthesis or extremely high temperatures, making it a scalable solution to prepare high-capacity anodes for next-generation LIBs.

  11. Facile synthesis and electrical switching properties of V{sub 2}O{sub 3} powders

    Energy Technology Data Exchange (ETDEWEB)

    Ji, Haining; Liu, Dongqing, E-mail: dongqingliu@ymail.com; Cheng, Haifeng; Yang, Lixiang; Zhang, Chaoyang; Zheng, Wenwei

    2017-03-15

    Highlights: • Single crystal uniform V{sub 2}O{sub 3} powders have been synthesized without additional surfactant. • Powders were obtained in only 6 h. • Powders exhibit reversible phase transition properties. • Powders have excellent electrical switching properties with resistance changes as large as 10{sup 4}. - Abstract: V{sub 2}O{sub 3} powders were synthesized with mercaptoacetic acid (C{sub 2}H{sub 4}O{sub 2}S) as reducing agent and stabilizer via a facile hydrothermal approach. The crystalline structure, surface morphology, valence state of the derived V{sub 2}O{sub 3} powders were characterized via X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy. It was found that the ratio and reaction time played a duel role in the formation and morphology of the V{sub 2}O{sub 3} powders. The metal-insulator transition properties of V{sub 2}O{sub 3} powders were studied by the differential scanning calorimetry curve and variable temperature Raman spectra. The change in electrical resistance due to the metal-insulator transition was measured from 80 to 240 K using physical property measurement system. The results showed V{sub 2}O{sub 3} samples had excellent electrical switching properties with resistance changes as large as 10{sup 4}. This simple and fast synthesis approach makes the V{sub 2}O{sub 3} powders easily accessible for exploring their fundamental properties and potential applications in novel electronic devices.

  12. Studies on the synthesis of nanocrystalline Y{sub 2}O{sub 3} and ThO{sub 2} through volume combustion and their sintering

    Energy Technology Data Exchange (ETDEWEB)

    Sanjay Kumar, D. [Fuel Chemistry Division, Chemistry Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102, Tamil Nadu (India); Ananthasivan, K., E-mail: asivan@igcar.gov.in [Fuel Chemistry Division, Chemistry Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102, Tamil Nadu (India); Venkata Krishnan, R. [Fuel Chemistry Division, Chemistry Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102, Tamil Nadu (India); Amirthapandian, S. [Material Physics Division, Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102, Tamil Nadu (India); Dasgupta, Arup [Microscopy and Thermo-Physical Property Division, Metallurgy and Materials Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102, Tamil Nadu (India)

    2016-10-15

    Volume combustion was observed in the auto-ignition of the citrate gels containing the nitrates of yttrium/thorium for the first time in mixture with a fuel (citric acid) to oxidant (Y{sup 3+} or Th{sup 4+} nitrate) ratio close to that demanded by the stoichiometry. These nanocrystalline powders were characterized for their bulk density, specific surface area, particle size distribution, carbon residue and X-ray crystallite size and were sintered by both the conventional and the two-step method. The maximum relative sintered density of Y{sub 2}O{sub 3} was 98.9% TD. The sintered density of thoria (97.8% TD) is the highest among the values reported so far, for nanocrystalline ThO{sub 2}. Characterization of the pellets and powders by using scanning electron microscopy and transmission electron microscopy reaffirmed nanocrystallinity and that the sintered pellets comprised faceted sintered grains. The two-step sintering was found to restrict “runaway” sintering. - Highlights: • Scaled-up synthesis of nanocrystalline Y{sub 2}O{sub 3} and ThO{sub 2} using citrate gel-combustion method. • VCR was observed at a fuel to nitrate ratio (R) of 0.125 and 0.17 in mixtures containing Th(NO{sub 3}){sub 4} and Y(NO{sub 3}){sub 3} respectively. • The calcined powders were compacted and sintered by using a novel two-step sintering method. • Sintered densities as high as 97.8% T.D. (ThO{sub 2}, T{sub H} = 0.48) and 98.9% T.D. (Y{sub 2}O{sub 3}, T{sub H} = 0.61) were obtained.

  13. Twenty-fifth symposium (international) on combustion

    International Nuclear Information System (INIS)

    Anon.

    1994-01-01

    Approximately two-thirds of the papers presented at this conference are contained in this volume. The other one-third appear in special issues of ''Combustion and Flame'', Vol. 99, 1994 and Vol. 100, 1995. Papers are divided into the following sections: Supersonic combustion; Detonations and explosions; Internal combustion engines; Practical aspects of combustion; Incineration and wastes; Sprays and droplet combustion; Coal and organic solids combustion; Soot and polycyclic aromatic hydrocarbons; Reaction kinetics; NO x ; Turbulent flames; Turbulent combustion; Laminar flames; Flame spread, fire and halogenated fire suppressants; Global environmental effects; Ignition; Two-phase combustion; Solid propellant combustion; Materials synthesis; Microgravity; and Experimental diagnostics. Papers have been processed separately for inclusion on the data base

  14. Urea-nitrate combustion synthesis of MgO/MgAl2O4 nanocatalyst used in biodiesel production from sunflower oil: Influence of fuel ratio on catalytic properties and performance

    International Nuclear Information System (INIS)

    Rahmani Vahid, Behgam; Haghighi, Mohammad

    2016-01-01

    Graphical abstract: As a base catalyst for biodiesel production, MgAl 2 O 4 spinel was successfully synthesized by combustion method with MgO, as the active phase, dispersed on the catalyst surface. The nanocatalysts were characterized by XRD, FESEM, EDX, BET-BJH, TGA and FTIR analyses, so as to optimize the concentration of urea (as fuel) in the combustion synthesis. Analyzing the effect of fuel ratio on the combustion synthesized MgAl 2 O 4 , it was revealed that the synthesized base catalyst with a fuel ratio of 1.5 was of the best specifications for biodiesel production process. Future researches may investigate the catalyst reusability and mild reaction conditions, so as to achieve more economical production of biodiesel. - Highlights: • Efficient synthesis of MgAl 2 O 4 spinel by solution combustion method. • Improvement of catalytic activity and stability by optimum ratio fuel. • Enhanced dispersion of MgO over MgAl 2 O 4 spinel. • Production of biodiesel over MgO/MgAl 2 O 4 at relatively mild reaction conditions. - Abstract: MgO/MgAl 2 O 4 nanocatalyst was synthesized by a simple, cost-effective and rapid method and used in biodiesel production from sunflower oil. MgAl 2 O 4 was synthesized by combustion method at different fuel ratios and then active phase of MgO was dispersed on the samples by impregnation method. The nanocatalysts were characterized by XRD, FESEM, EDX, BET-BJH, TGA and FTIR analyses, so as to optimize the concentration of urea (as fuel) in the combustion synthesis. The physicochemical properties of the nanocatalyst confirmed the sample synthesized with fuel ratio of 1.5 has high surface area, effective morphology and texture properties. Finally, in order to evaluate catalytic activity of the samples in biodiesel production, the transesterification reaction was performed. The results indicated the catalyst prepared by combustion synthesis with a fuel ratio of 1.5 was optimum specifications for biodiesel production. Using this

  15. Low-temperature metal-oxide thin-film transistors formed by directly photopatternable and combustible solution synthesis.

    Science.gov (United States)

    Rim, You Seung; Lim, Hyun Soo; Kim, Hyun Jae

    2013-05-01

    We investigated the formation of ultraviolet (UV)-assisted directly patternable solution-processed oxide semiconductor films and successfully fabricated thin-film transistors (TFTs) based on these films. An InGaZnO (IGZO) solution that was modified chemically with benzoylacetone (BzAc), whose chelate rings decomposed via a π-π* transition as result of UV irradiation, was used for the direct patterning. A TFT was fabricated using the directly patterned IGZO film, and it had better electrical characteristics than those of conventional photoresist (PR)-patterned TFTs. In addition, the nitric acid (HNO3) and acetylacetone (AcAc) modified In2O3 (NAc-In2O3) solution exhibited both strong UV absorption and high exothermic reaction. This method not only resulted in the formation of a low-energy path because of the combustion of the chemically modified metal-oxide solution but also allowed for photoreaction-induced direct patterning at low temperatures.

  16. Combustion synthesis by reaction and characterization of nano ferrites: study of fuel aniline, citric and its mixture

    International Nuclear Information System (INIS)

    Silva, M.C. da; Coutinho, J.P.; Costa, A.C.F.M.; Kiminami, R.H.G.A.; Freitas, N.L. de

    2012-01-01

    The present study aims to evaluate the influence of aniline and citric acid used alone and combined in a ratio of 50% each in the characterization of NiZn ferrite synthesized by combustion reaction method in a muffle furnace. Measurements were made of temperature and reaction time. The nano-powders were characterized by XRD, EDX, textural analysis and SEM. The highest temperature was achieved by the reaction using the mixture of fuel and increased reaction time using citric acid. The nano ferrites using different fuels, and the mixture changed phases, the crystallite size and decreased surface area of the samples with aniline, citric acid and a mixture of both, respectively. The powder morphology ranged from presenting the formation of irregular blocks for the use of citric agglomerated in the form of skeins with aniline and a mixture to agglomerate larger particles. (author)

  17. Sol-gel auto-combustion synthesis and properties of Co2Z-type hexagonal ferrite ultrafine powders

    Science.gov (United States)

    Liu, Junliang; Yang, Min; Wang, Shengyun; Lv, Jingqing; Li, Yuqing; Zhang, Ming

    2018-05-01

    Z-type hexagonal ferrite ultrafine powders with chemical formulations of (BaxSr1-x)3Co2Fe24O41 (x varied from 0.0 to 1.0) have been synthesized by a sol-gel auto-combustion technique. The average particle sizes of the synthesized powders ranged from 2 to 5 μm. The partial substitution of Ba2+ by Sr2+ led to the shrinkage of the crystal lattices and resulted in changes in the magnetic sub-lattices, which tailored the static and dynamic magnetic properties of the as-synthesized powders. As the substitution ratio of Ba2+ by Sr2+, the saturation magnetization of the synthesized powders almost consistently increased from 43.3 to 56.1 emu/g, while the real part of permeability approached to a relatively high value about 2.2 owing to the balance of the saturation magnetization and magnetic anisotropy field.

  18. Synthesis by combustion reaction of ZnAl2O4 and application in methyl alcoholysis of soybean oil

    International Nuclear Information System (INIS)

    Dantas, B.B.; Silva, A.S.; Cunha, R.B.L.; Leal, E.; Costa, A.C.F.M.

    2011-01-01

    Biodiesel currently presents itself as a viable alternative to diesel oil front. However, implementation of actions most economic use as heterogeneous catalysts, allows further reduction of this biofuel by procedural steps. This work was supported application of catalytic ZnAl 2 O 4 obtained by combustion reaction in methyl alcoholysis of soybean oil. Samples of the supports were characterized by XRD, textural analysis by nitrogen adsorption and FTIR. The reaction tests were performed at 200°C, molar ratio 1:25, 2 and 4 wt% of catalyst and reaction time of 3 hours. XRD results indicate that the phase was obtained ZnAl 2 O 4 effectively, with surface areas of 14.9 and 8.6 m 2 g -1 . The tests demonstrated that reactional higher content of ester was 56.1 and 63.1% for the percentage of catalyst 2 and 4% respectively. (author)

  19. A facile and rapid automated synthesis of 3'-deoxy-3'-[18F]fluorothymidine

    International Nuclear Information System (INIS)

    Tang Ganghua; Tang Xiaolan; Wen Fuhua; Wang Mingfang; Li Baoyuan

    2010-01-01

    Aim: To develop a simplified and fully automated synthesis procedure of 3'-deoxy-3'-[ 18 F]fluorothymidine ([ 18 F]FLT) using PET-MF-2V-IT-I synthesis module. Methods: Synthesis of [ 18 F]FLT was performed using PET-MF-2V-IT-I synthesis module by one-pot two-step reaction procedure, including nucleophilic fluorination of 3-N-t-butoxycarbonyl-1-[5'-O-(4,4'-dimethoxy triphenylmethyl)-2'-deoxy-3'-O-(4-nitrobenzenesulfonyl) -β-D-threopentofuranosyl]thymine (15 mg) as the precursor molecule with [ 18 F]fluoride, and subsequent hydrolysis of the protecting group with 1.0 M HCl at the same reaction vessel and purification with SEP PAK cartridges instead of the HPLC system. Results: The automated synthesis of [ 18 F]FLT with SEP PAK purification gave corrected radiochemical yield of 23.2±2.6% (n=6, uncorrected yield: 16-22%) and radiochemical purity of >97% within the total synthesis time of 35 min. Conclusion: The fully one-pot automated synthesis procedure with SEP PAK purification can be applied to the fully automated synthesis of [ 18 F]FLT using commercial [ 18 F]FDG synthesis module.

  20. Detonation cell size measurements in high-temperature hydrogen-air-steam mixtures at the BNL high-temperature combustion facility

    International Nuclear Information System (INIS)

    Ciccarelli, G.; Ginsberg, T.; Boccio, J.L.

    1997-11-01

    The High-Temperature Combustion Facility (HTCF) was designed and constructed with the objective of studying detonation phenomena in mixtures of hydrogen-air-steam at initially high temperatures. The central element of the HTCF is a 27-cm inner-diameter, 21.3-m long cylindrical test vessel capable of being heating to 700K ± 14K. A unique feature of the HTCF is the 'diaphragmless' acetylene-oxygen gas driver which is used to initiate the detonation in the test gas. Cell size measurements have shown that for any hydrogen-air-steam mixture, increasing the initial mixture temperature, in the range of 300K to 650K, while maintaining the initial pressure of 0.1 MPa, decreases the cell size and thus makes the mixture more detonable. The effect of steam dilution on cell size was tested in stoichiometric and off-stoichiometric (e.g., equivalence ratio of 0.5) hydrogen-air mixtures. Increasing the steam dilution in hydrogen-air mixtures at 0.1 MPa initial pressure increases the cell size, irrespective of initial temperature. It is also observed that the desensitizing effect of steam diminished with increased initial temperature. A 1-dimensional, steady-state Zel'dovich, von Neumann, Doring (ZND) model, with full chemical kinetics, has been used to predict cell size for hydrogen-air-steam mixtures at different initial conditions. Qualitatively the model predicts the overall trends observed in the measured cell size versus mixture composition and initial temperature and pressure. It was found that the proportionality constant used to predict detonation cell size from the calculated ZND model reaction zone varies between 10 and 100 depending on the mixture composition and initial temperature. 32 refs., 35 figs

  1. Facile synthesis, spectral properties and formation mechanism of sulfur nanorods in PEG-200

    International Nuclear Information System (INIS)

    Xie, Xin-yuan; Li, Li-yun; Zheng, Pu-sheng; Zheng, Wen-jie; Bai, Yan; Cheng, Tian-feng; Liu, Jie

    2012-01-01

    Graphical abstract: Homogeneous rod-like structure of sulfur with a typical diameter of about 80 nm and an average aspect ratio of about 6–8 was obtained. The sulfur nanoparticles could self-assemble from spherical particles to nanorods in PEG-200. During the self-assembling process, the absorption band showed a red shift which was due to the production of nanorods. Highlights: ► A novel, facile and greener method to synthesize sulfur nanorods by the solubilizing and templating effect of PEG-200 was reported. ► S 0 nanoparticles could self assemble in PEG-200 and finally form monodisperse and homogeneous rod-like structure with an average diameter of about 80 nm, the length ca. 600 nm. ► The absorption band showed a red shift and the RRS intensity enhanced continuously during the self-assembling process. ► PEG-200 induced the oriented attachment of sulfur nanoparticles by the terminal hydroxyl groups. -- Abstract: The synthesis of nano-sulfur sol by dissolving sublimed sulfur in a green solvent-PEG-200 was studied. Homogeneous rod-like structure of sulfur with a typical diameter of about 80 nm and an average aspect ratio of 6–8 was obtained. The structure, morphology, size, and stability of the products were investigated by transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and dynamic light scattering (DLS) measurements. The spectral properties of the products were investigated by ultraviolet-visible (UV–vis) absorption and resonance Rayleigh scattering spectroscopy (RRS). The results showed that the spherical sulfur nanoparticles could self-assemble into nanorods in PEG-200. During the self-assembling process, the absorption band showed a red shift and the RRS intensity enhanced continuously. There was physical cross-linking between PEG and sulfur nanoparticles. PEG-200 induced the oriented attachment of sulfur nanoparticles by the

  2. Facile synthesis of silver immobilized-poly(methyl methacrylate)/polyethyleneimine core-shell particle composites

    Energy Technology Data Exchange (ETDEWEB)

    Jenjob, Somkieath [Department of Chemistry, Faculty of Science, Mahidol University, 999 Phuttamonthon 4 Road, Salaya, Nakhon Pathom 73170 (Thailand); Center of Excellence for Innovation in Chemistry (PERCH-CIC), Department of Chemistry, Faculty of Science, Mahidol University, Rama 6 Road, Ratchathewi, Bangkok 10400 (Thailand); Tharawut, Teeralak [Department of Chemistry, Faculty of Science, Mahidol University, 999 Phuttamonthon 4 Road, Salaya, Nakhon Pathom 73170 (Thailand); Sunintaboon, Panya, E-mail: panya.sun@mahidol.ac.th [Department of Chemistry, Faculty of Science, Mahidol University, 999 Phuttamonthon 4 Road, Salaya, Nakhon Pathom 73170 (Thailand); Center of Excellence for Innovation in Chemistry (PERCH-CIC), Department of Chemistry, Faculty of Science, Mahidol University, Rama 6 Road, Ratchathewi, Bangkok 10400 (Thailand); Center for Alternative Energy, Faculty of Science, Mahidol University, 999 Phuttamonthon 4 Road, Salaya, Nakhon Pathom 73170 (Thailand)

    2012-10-01

    A facile route to synthesize silver-embedded-poly(methyl methacrylate)/polyethyleneimine (PMMA/PEI-Ag) core-shell particle composites was illustrated in this present work. PMMA/PEI core-shell particle templates were first prepared by a surfactant-free emulsion polymerization. PEI on the templates' surface was further used to complex and reduce Ag{sup +} ions (from silver nitrate solution) to silver nanoparticles (AgNPs) at ambient temperature, resulting in the PMMA/PEI-Ag particle composites. The formation of AgNPs was affected by the pHs of the reaction medium. The pH of reaction medium at 6.5 was optimal for the formation of PMMA/PEI-Ag with good colloidal stability, which was confirmed by size and size distribution, FTIR spectroscopy, UV-vis spectroscopy and X-ray diffraction. Moreover, the amount of AgNO{sub 3} solution (4.17-12.50 g) was found to affect the formation of AgNPs. Transmission electron microscopy (TEM) indicated that the AgNPs were incorporated in the PMMA/PEI core-shell matrix, and had 6-10 nm in diameter. AgNPs immobilized on PMMA/PEI core-shell particles were also investigated by energy dispersive X-ray spectroscopy analysis mode extended from scanning electron microscopy (SEM/EDS). Furthermore, the presence of AgNPs was found to influence the thermal degradation behavior of PMMA/PEI particle composites as observed through thermogravimetric analysis (TGA). Highlights: Black-Right-Pointing-Pointer A 2-step synthesis of Ag immobilized-PMMA/PEI particle composites was shown. Black-Right-Pointing-Pointer PMMA/PEI core-shell templates were first formed and PEI assisted AgNP formation. Black-Right-Pointing-Pointer Formation of PMMA/PEI-Ag was affected by pH of medium and amount of AgNO{sub 3}. Black-Right-Pointing-Pointer PMMA/PEI-Ag can be confirmed by color change, UV-vis, TEM, SEM with EDS, and X-ray. Black-Right-Pointing-Pointer Effect of AgNPs on thermal degradation of PMMA/PEI-Ag can be observed through TGA.

  3. Influence of different fuel agents on the combustion synthesis of the nanostructured Li{sub 1.05}Mn{sub 2}O{sub 4} oxide

    Energy Technology Data Exchange (ETDEWEB)

    Amaral, Fabio A.; Guerra, R.F.; Santana, L.K.; Canobre, S.C., E-mail: fabioamaral@iqufu.ufu.br [Universidade Federal de Uberlandia (LAETE/UFU), MG (Brazil). Inst. de Quimica. Lab. de Armazenamento de Energia e Tratamento de Efluentes

    2014-08-15

    In this work nanostructured Li{sub 1.05}Mn{sub 2}O{sub 4} oxide was obtained by Solution Combustion Synthesis (SCS) using three different fuel agents in order to obtain a unique phase with a crystalline cubic structure belonging to the F{sub d3m} spatial group. The phase of interest could be obtained, following the order: glycine (at 600 °C for 2 h) ‹ urea (at 750 °C for 2 h) ‹ maleic anhydride (at 750 °C for 4 h), with crystallite size in the range from 4.6 to 9.7 nm (nanometric character) and the unit cell parameter of the calcined samples at 750 °C for 2 h were similar to the JCPDS 35-0782 with cubic structure (a = 8.247 Å). Charge and discharge tests from the samples obtained by glycine fuel (at 750 °C for 4 h) presented the highest experimental specific capacities of 115 mA h g{sup -1} and 92% of retention after 10 cycles. (author)

  4. Improved dehydriding property of polyvinylpyrrolidone coated Mg-Ni hydrogen storage nano-composite prepared by hydriding combustion synthesis and wet mechanical milling

    Directory of Open Access Journals (Sweden)

    Linglong Yao

    2018-02-01

    Full Text Available In this work, polyvinylpyrrolidone (PVP coated Mg95Ni5 nano-composites were prepared by hydriding combustion synthesis (HCS plus wet mechanical milling (WM with tetrahydrofuran (THF and donated as WM-x wt% PVP (x = 1, 3, 5 and 7 respectively. The phase compositions, microstructures and dehydriding property, as well as the co-effect of PVP and THF were investigated in detail. XRD results showed that the average crystal size of MgH2 in the milled Mg95Ni5 decreased from 23 nm without PVP to 18 nm with 1 wt% PVP. The peak temperature of dehydrogenation of MgH2 in the milled Mg95Ni5 decreased from 293.0 °C without THF to 250.4 °C with THF. The apparent activation energy for decomposition of MgH2 in WM-7 wt% PVP was estimated to be 66.94 kJ/mol, which is 37.70 kJ/mol lower than that of milled Mg95Ni5 without THF and PVP. PVP and THF can facilitate the refinement of particle size during mechanical milling process. Attributed to small particle sizes and synergistic effect of PVP and THF, the composites exhibit markedly improved dehydriding properties. Keywords: Mg-Ni-PVP, Composite, Mg-based alloy, Wet mechanical milling, Dehydriding temperature

  5. Microwave-Assisted Combustion Synthesis of Nano Iron Oxide/Iron-Coated Activated Carbon, Anthracite, Cellulose Fiber, and Silica, with Arsenic Adsorption Studies

    Directory of Open Access Journals (Sweden)

    Mallikarjuna N. Nadagouda

    2011-01-01

    Full Text Available Combustion synthesis of iron oxide/iron coated carbons such as activated carbon, anthracite, cellulose fiber, and silica is described. The reactions were carried out in alumina crucibles using a Panasonic kitchen microwave with inverter technology, and the reaction process was completed within a few minutes. The method used no additional fuel and nitrate, which is present in the precursor itself, to drive the reaction. The obtained samples were then characterized with X-ray mapping, scanning electron microscopy (SEM, energy dispersive X-ray analysis (EDS, selected area diffraction pattern (SAED, transmission electron microscopy (TEM, X-ray diffraction (XRD, and inductively coupled plasma (ICP spectroscopy. The size of the iron oxide/iron nanoparticle-coated activated carbon, anthracite, cellulose fiber, and silica samples were found to be in the nano range (50–400 nm. The iron oxide/iron nanoparticles mostly crystallized into cubic symmetry which was confirmed by SAED. The XRD pattern indicated that iron oxide/iron nano particles existed in four major phases. That is, γ-Fe2O3, α-Fe2O3, Fe3O4, and Fe. These iron-coated activated carbon, anthracite, cellulose fiber, and silica samples were tested for arsenic adsorption through batch experiments, revealing that few samples had significant arsenic adsorption.

  6. Fabrication of Cu-riched W–Cu composites by combustion synthesis and melt-infiltration in ultrahigh-gravity field

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Pei [Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100039 (China); Guo, Shibin; Liu, Guanghua; Chen, Yixiang [Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190 (China); Li, Jiangtao, E-mail: ljt0012@vip.sina.com [Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190 (China)

    2013-10-15

    Unadulterated Cu-riched W–Cu composites of W27–Cu73, W34–Cu66, W40–Cu60, W49–Cu51 and W56–Cu44 have been prepared by a novel method called combustion synthesis and melt-infiltration in ultrahigh-gravity field, of which W27–Cu73 and W34–Cu66 showed good ductility and W40–Cu60, W49–Cu51 and W56–Cu44 were brittle. In this technique, Cu melt accompanied with a great amount of heat was produced by thermit reaction and infiltrated into W–Cu powder bed. When the powder bed was Cu-riched powder bed such as W50–Cu50 or W60–Cu40, Cu melt would go through the powder bed, reach the bottom of the graphite crucible and then form a heat dissipation channel. Thus the cooling rate was so fast that the product was mixed up with impurity. The problem can be solved by putting some W powders under W50–Cu50 or W60–Cu40 powder bed to prevent the formation of heat dissipation channel.

  7. Layered Composite of TiC-TiB2 to Ti-6Al-4V in Graded Composition by Combustion Synthesis in High-gravity Field

    International Nuclear Information System (INIS)

    Huang Xuegang; Zhao Zhongmin; Zhang Long

    2013-01-01

    By taking combustion synthesis to prepare solidified TiB 2 matrix ceramic in high-gravity field, the layered composite of TiC-TiB 2 ceramic to Ti-6Al-4V substrate in graded composition was achieved. XRD, FESEM and EDS results showed that the bulk full-density solidified TiC-TiB 2 composite was composed of fine TiB 2 platelets, TiC irregular grains, a few of α-Al 2 O 3 inclusions and Cr alloy phases, and α'-Ti phases alternating with Ti-enriched carbides constituted the matrix of the joint in which fine TiB platelets were embedded, whereas some C, B atoms were also detected at the heat-affected zone of Ti-6A1-4V substrate. The layered composite of the solidified ceramic to Ti-6Al-4V substrate in graded composition with continuous microstructure was considered a result of fused joint and inter-diffusion between liquid ceramic and surface-molten Ti alloy, followed by TiB 2 -Ti peritectic reaction and subsequent eutectic reaction in TiC-TiB-Ti ternary system.

  8. Preparation of LiMn2O4 Graphene Hybrid Nanostructure by Combustion Synthesis and Their Electrochemical Properties

    Directory of Open Access Journals (Sweden)

    Dinesh Rangappa

    2014-10-01

    Full Text Available The LiMn2O4 graphene hybrid cathode material has been synthesized by spray drying combustion process. The spinel structure cubic phase LiMn2O4 graphene hybrid material was prepared by spray drying process at 120 ℃ and subsequent heat treatment at 700 ℃ for 1 hour. The result indicates that the spinel shaped LiMn2O4 particles wrapped with graphene sheets were formed with particle size in the range of 60-70 nm. The charge-discharge measurement indicates that the LiMn2O4 graphene hybrid material shows an improved discharge capacity of 139 mAh/g at 0.1C rate. The pristine LiMn2O4 nano crystals present only about 132 mAh/g discharge capacity. The LiMn2O4 graphene hybrid samples show good cyclic performance with only 13% of capacity fading in 30 cycles when compared to the pristine LiMn2O4 that shows 22% of capacity fading in 30 cycles. The capacity retention of the LiMn2O4 graphene hybrid samples is about 10% higher than the pristine cycle after 30 cycles.

  9. Evaluation of the urea content in the synthesis by combustion reaction of the NiAl2O4 catalysts

    International Nuclear Information System (INIS)

    Leal, E.; Sousa, J.-P.L.M.L.; Costa, A.C.F.M.; Gama, L.; Argolo, F.; Sasaki, J.M.

    2009-01-01

    The aim of this work is to evaluate the influence of the urea fuel in the structure and morphology of the NiAl 2 O 4 prepared by combustion reaction. The powders were prepared according to the propellants and explosives theory, using urea in the stoichiometric composition, with 10% of excess and deficiency of this fuel. The samples were characterized by XRD, FTIR, particle size distribution and textural analysis by nitrogen adsorption (BET/BJH). The DRX results showed the presence of NiAl 2 O 4 as major phase and traces of NiO for all the samples. Also show crystallites size between 13 and 21 nm. All the samples showed large agglomerates size distribution, with D 50% between 18.6 and 20.4 μm, and morphology with irregular plates shape. The increase of the urea content caused an increase in the particle size and a reduction in the surface area, from 270 to 52 m 2 /g. (author)

  10. Synthesis and characterization of nickel substituted cobalt ferrite nanoparticles by sol–gel auto-combustion method

    Energy Technology Data Exchange (ETDEWEB)

    Hankare, P.P., E-mail: p_hankarep@rediffmail.com [Solid State Research Laboratory, Department of Chemistry, Shivaji University, Kolhapur, Maharashtra 416 004 (India); Sanadi, K.R., E-mail: sanadikishor@gmail.com [Solid State Research Laboratory, Department of Chemistry, Shivaji University, Kolhapur, Maharashtra 416 004 (India); Garadkar, K.M. [Solid State Research Laboratory, Department of Chemistry, Shivaji University, Kolhapur, Maharashtra 416 004 (India); Patil, D.R. [Material Research Laboratory, Department of Physics, R.L. College, Parola, Jalgaon, Maharashtra 425 111 (India); Mulla, I.S. [Emeritus Scientist-CSIR, Centre for Materials for Electronics and Technology (C-MET), Panchawati, Pune 411 008 (India)

    2013-03-15

    Highlights: ► Co{sub 1−x}Ni{sub x}Fe{sub 2}O{sub 4} Mixed Metal oxides. ► Sol–gel auto-combustion method. ► Cubic spinel symmetry. ► Nanocrystaline material. ► Semiconducting nature. -- Abstract: Nanocrystalline Co{sub 1−x}Ni{sub x}Fe{sub 2}O{sub 4} (where x = 0.0, 0.25, 0.50, 0.75, 1) were successfully synthesized by sol–gel method using citrate–nitrate precursors. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were effectively utilized to investigate the different structural parameters. XRD showed single cubic spinel phase for all the samples. The decrease in lattice parameter and increase in crystallite size of the ferrispinel was observed with increasing nickel content. The surface morphology and elemental composition were studied by Scanning electron microscope (SEM) and Energy Dispersive X-ray analysis (EDAX) respectively. The nanosize of the synthesized material had been identified by TEM investigation and which is lies in between 20–25 nm. The semiconducting nature of the samples was studied by variation of resistivity and thermal emf with temperature.

  11. Facile synthesis of soluble functional graphene by reduction of graphene oxide via acetylacetone and its adsorption of heavy metal ions

    International Nuclear Information System (INIS)

    Xu, Minghan; Chai, Jing; Hu, Nantao; Huang, Da; Wang, Yuxi; Huang, Xiaolu; Wei, Hao; Yang, Zhi; Zhang, Yafei

    2014-01-01

    The synthesis of graphene (GR) from graphene oxide (GO) typically involves harmful chemical reducing agents that are undesirable for most practical applications. Here we report a green and facile synthesis method for the synthesis of GR that is soluble in water and organic solvents and that includes the additional benefit of adsorption of heavy metal ions. Acetylacetone, as both a reducing agent and a stabilizer, was used to prepare soluble GR from GO. Transmission electron microscopy and atomic force microscopy provide clear evidence for the formation of few-layer GR. The results from Fourier transform infrared spectroscopy and ultraviolet-visible spectroscopy show that reduction of GO to GR has occurred. Raman spectroscopy and X-ray photoelectron spectroscopy also indicate the removal of oxygen-containing functional groups from GO, resulting in the formation of GR. The results of dispersion experiments show that GR can be highly dispersed in water and N,N-Dimethylformamide. The reaction mechanism for acetylacetone reduction of exfoliated GO was also proposed. This method is a facile and environmentally friendly approach to the synthesis of GR and opens up new possibilities for preparing GR and GR-based nanomaterials for large-scale applications. Of even greater interest is that inductively coupled plasma atomic emission spectroscopy suggests that synthesized GR may be applied in the absorption of Cd 2+ and Co 2+ due to the strong coordination capacity of acetylacetone on the surfaces and edges of GR and the large surface area of GR in aqueous solutions. The maximum adsorptions are 49.28 mg g −1 for Cd 2+ , which is 4.5 times higher than that of carbon nanotubes, and 27.78 mg g −1 for Co 2+ , which is 3.6 times higher than that of titania beans. (paper)

  12. Facile synthesis of porous Pt-Pd nanospheres supported on reduced graphene oxide nanosheets for enhanced methanol electrooxidation

    Science.gov (United States)

    Li, Shan-Shan; Lv, Jing-Jing; Hu, Yuan-Yuan; Zheng, Jie-Ning; Chen, Jian-Rong; Wang, Ai-Jun; Feng, Jiu-Ju

    2014-02-01

    In this study, a simple, facile, and effective wet-chemical strategy was developed in the synthesis of uniform porous Pt-Pd nanospheres (Pt-Pd NSs) supported on reduced graphene oxide nanosheets (RGOs) under ambient temperature, where octylphenoxypolye thoxyethanol (NP-40) is used as a soft template, without any seed, organic solvent or special instruments. The as-prepared nanocomposites display enhanced electrocatalytic activity and good stability toward methanol oxidation, compared with commercial Pd/C and Pt/C catalysts. This strategy may open a new route to design and prepare advanced electrocatalysts for fuel cells.

  13. Combustion engineering

    CERN Document Server

    Ragland, Kenneth W

    2011-01-01

    Introduction to Combustion Engineering The Nature of Combustion Combustion Emissions Global Climate Change Sustainability World Energy Production Structure of the Book   Section I: Basic Concepts Fuels Gaseous Fuels Liquid Fuels Solid Fuels Problems Thermodynamics of Combustion Review of First Law Concepts Properties of Mixtures Combustion StoichiometryChemical EnergyChemical EquilibriumAdiabatic Flame TemperatureChemical Kinetics of CombustionElementary ReactionsChain ReactionsGlobal ReactionsNitric Oxide KineticsReactions at a Solid SurfaceProblemsReferences  Section II: Combustion of Gaseous and Vaporized FuelsFlamesLaminar Premixed FlamesLaminar Flame TheoryTurbulent Premixed FlamesExplosion LimitsDiffusion FlamesGas-Fired Furnaces and BoilersEnergy Balance and EfficiencyFuel SubstitutionResidential Gas BurnersIndustrial Gas BurnersUtility Gas BurnersLow Swirl Gas BurnersPremixed-Charge Engine CombustionIntroduction to the Spark Ignition EngineEngine EfficiencyOne-Zone Model of Combustion in a Piston-...

  14. An efficient and facile synthesis of divergent C-3/C-5 bis ...

    Indian Academy of Sciences (India)

    extensive attention in organic synthesis and also serve as potential synthons for the ... plays an important role in synthetic chemistry, because they also serve as ...... scope, rate acceleration and selective formation of bis-. MBH adduct with ...

  15. Synthesis of yttrium oxide nanoparticles via a facile microplasma-assisted process

    NARCIS (Netherlands)

    Lin, Liangliang; Starostin, Sergey A.; Li, Sirui; Khan, Saif A.; Hessel, Volker

    2018-01-01

    Plasma electrochemistry is an emerging technique for nanomaterial synthesis. The present study reports the preparation of yttrium oxide nanoparticles via a simple, environmentally benign, microplasma-assisted process operated in pin-to-liquid configuration under ambient atmospheric conditions using

  16. Double reductive cyclization: A facile synthesis of the indoloquinoline alkaloid cryptotackieine

    Digital Repository Service at National Institute of Oceanography (India)

    Parvatkar, P.T.; Parameswaran, P.S.; Tilve, S.G.

    A new synthesis of the indoloquinoline alkaloid cryptotackieine, isolated from Cryptolepis sanguinolenta, is described which involves a Perkin reaction, a tandem double reduction-double cyclization reaction followed by regioselective methylation...

  17. A Facile and Efficient Synthesis of (15R)-Latanoprost from Chiral ...

    Indian Academy of Sciences (India)

    aDepartment of Chemistry, JNTUH College of Engineering Jagtial, ... is not effective with these topically applied drugs, ... approaches for the synthesis of latanoprost.7 Recently, ... lected organic layer was washed with brine solution and.

  18. Thermally stimulated luminescence and persistent luminescence of β-irradiated YAG:Pr"3"+ nanophosphors produced by combustion synthesis

    International Nuclear Information System (INIS)

    Santacruz-Gomez, K.; Meléndrez, R.; Gil-Tolano, M.I.; Jimenez, J.A.; Makale, M.T.; Barboza-Flores, M.; Castaneda, B.; Soto-Puebla, D.; Pedroza-Montero, M.; McKittrick, J.; Hirata, G.A.

    2016-01-01

    In this work, the thermally stimulated luminescence (TSL) and persistent luminescence (PLUM) properties of praseodymium doped yttrium aluminum garnet (YAG:Pr"3"+) exposed to β-irradiation are reported. X-ray diffraction (XRD) confirms a single phase of YAG obtained by the combustion method. Transmission electron microscopy (TEM) shows that powder particles appear to be irregular crystals with an average size of 67 nm. TSL glow-curve deconvolution of YAG:Pr"3"+ after β-irradiation consist in six peaks centered at 394, 450, 467, 543, 637 and 705 K. The TSL fading and PLUM signals were found to be associated with at least with two different kinds of traps, corresponding to the peaks located at 394, 450 and 467 K. YAG:Pr"3"+ nanophosphors analyzed in this work showed interesting features about the dosimetric sensitivity as well as the reproducibility for both TSL/PLUM techniques, with good linearity dose response. These results indicate that nanocrystalline YAG:Pr3"+ is a good candidate for dosimetric applications in the range of 80 mGy-20 Gy. - Highlights: • β-irradiated YAG:Pr"3"+ TSL consist in 394, 450, 467, 543, 637 and 705 K peaks. • YAG:Pr"3"+ is a good candidate for dosimetry in the range of 80 mGy-20 Gy. • PLUM can be potentially used for in vivo, in situ and quasi in real time dosimetry.

  19. Particle size, morphology and color tunable ZnO:Eu{sup 3+} nanophosphors via plant latex mediated green combustion synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Chandrasekhar, M. [Prof. C.N.R. Rao Centre for Advanced Materials, Tumkur University, Tumkur 572 103 (India); Department of Physics, Acharya Institute of Technology, Bangalore 560 107 (India); Nagabhushana, H., E-mail: bhushanvlc@gmail.com [Prof. C.N.R. Rao Centre for Advanced Materials, Tumkur University, Tumkur 572 103 (India); Sharma, S.C. [B.S. Narayan Centre of Excellence for Advanced Materials, B.M.S. Institute of Technology, Yelahanka, Bangalore 560 064 (India); Department of Mechanical Engineering, B.M.S. Institute of Technology, Yelahanka, Bangalore 560 064 (India); Sudheer kumar, K.H. [Department of Environmental Science, Kuvempu University, Shankarghatta, Shimoga 577 451 (India); Department of Chemistry, B.M.S. Institute of Technology, Yelahanka, Bangalore 560 064 (India); B.S. Narayan Centre of Excellence for Advanced Materials, B.M.S. Institute of Technology, Yelahanka, Bangalore 560 064 (India); Dhananjaya, N. [Department of Physics, B.M.S. Institute of Technology, Yelahanka, Bangalore 560 064 (India); B.S. Narayan Centre of Excellence for Advanced Materials, B.M.S. Institute of Technology, Yelahanka, Bangalore 560 064 (India); Sunitha, D.V. [Prof. C.N.R. Rao Centre for Advanced Materials, Tumkur University, Tumkur 572 103 (India); Shivakumara, C. [Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore 560 012 (India); Nagabhushana, B.M. [Department of Chemistry, M.S. Ramaiah Institute of Technology, Bangalore 560 054 (India)

    2014-01-25

    Highlights: • ZnO:Eu{sup 3+} phosphors were prepared by green synthesis route. • Morphology and particle size was tuned by varying the concentration of plant latex. • The phosphor show excellent chromaticity coordinates in the white region. -- Abstract: Efficient ZnO:Eu{sup 3+} (1–11 mol%) nanophosphors were prepared for the first time by green synthesis route using Euphorbia tirucalli plant latex. The final products were well characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–visible spectroscopy (UV–Vis), Fourier transform infrared spectroscopy (FTIR), etc. The average particle size of ZnO:Eu{sup 3+} (7 mol%) was found to be in the range 27–47 nm. With increase of plant latex, the particle size was reduced and porous structure was converted to spherical shaped particles. Photoluminescence (PL) spectra indicated that the peaks situated at ∼590, 615, 648 and 702 nm were attributed to the {sup 5}D{sub 0} → {sup 7}F{sub j(j=1,2,3,4)} transitions of Eu{sup 3+} ions. The highest PL intensity was recorded for 7 mol% with Eu{sup 3+} ions and 26 ml plant latex concentration. The PL intensity increases with increase of plant latex concentration up to 30 ml and there after it decreases. The phosphor prepared by this method show spherical shaped particles, excellent chromaticity co-ordinates in the white light region which was highly useful for WLED’s. Further, present method was reliable, environmentally friendly and alternative to economical routes.

  20. Fuel effect on solution combustion synthesis of Co(Cr,Al)2O4 pigments; Efecto del combustible en la síntesis de pigmentos Co(Cr,Al)2O4 por combustión de una disolución

    Energy Technology Data Exchange (ETDEWEB)

    Gilabert, J.; Palacios, M.D.; Sanz, V.; Mestre, S.

    2017-11-01

    The fuel effect on the synthesis of a ceramic pigment with a composition CoCr2−2ΨAl2ΨO4 (0≤Ψ≤1) by means of solution combustion synthesis process (SCS) has been studied. Three different fuels were selected to carry out the synthesis (urea, glycine and hexamethylentetramine (HMT)). Highly foamy pigments with very low density were obtained. Fd-3m spinel-type structure was obtained in all the experiments. Nevertheless, crystallinity and crystallite size of the spinels show significant differences with composition and fuel. The use of glycine along with the chromium-richest composition favours ion rearrangement to obtain the most ordered structure. Lattice parameter does not seem to be affected by fuel, although it evolves with Ψ according to Vegard's law. Colouring power in a transparent glaze shows important variations with composition. On the other hand, fuel effect presents a rather low influence since practically the same shades are obtained. However, it exerts certain effect on luminosity (L*). [Spanish] Se ha estudiado el efecto del combustible en la síntesis de pigmentos cerámicos tipo CoCr2-2ΨAl2ΨO4 (0≤Ψ≤1), obtenidos mediante síntesis por combustión de una disolución. Se seleccionaron 3 tipos de combustible diferentes: urea, glicina y hexametilentetramina. Todos los pigmentos obtenidos presentaron una textura altamente esponjosa y con muy baja densidad. Las estructuras cristalinas desarrolladas en todos los casos fueron tipo espinela Fd-3m. Sin embargo, tanto la cristalinidad como el tamaño de cristalito presentaron diferencias significativas dependiendo de la composición y del combustible utilizado. El uso de glicina, junto con las composiciones más ricas en cromo, favorece la reorganización de los iones para obtener estructuras más ordenadas y con mayor cristalinidad. El parámetro de red no parece verse afectado por el combustible, aunque sí evoluciona con Ψ de acuerdo con la Ley de Vegard. El poder colorante desarrollado

  1. Facile Synthesis and High performance of a New Carbazole-Based Hole Transporting Material for Hybrid Perovskite Solar Cells

    KAUST Repository

    Wang, Hong

    2015-06-26

    Perovskite solar cells are very promising for practical applications owing to their rapidly rising power conversion efficiency and low cost of solution-based processing. 2,2’,7,7’-tetrakis-(N,N-di-p-methoxyphenylamine) 9,9’-spirobifluorene (Spiro-OMeTAD) is most widely used as hole transporting material (HTM) in perovskite solar cells. However, the tedious synthesis and high cost of Spiro-OMeTAD inhibit its commercial-scale application in the photovoltaic industry. In this article, we report a carbazole-based compound (R01) as a new HTM in efficient perovskite solar cells. R01 is synthesized via a facile route consisting of only two steps from inexpensive commercially available materials. Furthermore, R01 exhibits higher hole mobility and conductivity than the state-of-the-art Spiro-OMeTAD. Perovskite solar cells fabricated with R01 produce a power conversion efficiency of 12.03%, comparable to that obtained in devices using Spiro-OMeTAD in this study. Our findings underscore R01 as a highly promising HTM with high performance, and its facile synthesis and low cost may facilitate the large-scale applications of perovskite solar cells.

  2. Facile Conversion Synthesis of Densely-Formed Branched ZnO-Nanowire Arrays for Quantum-Dot-Sensitized Solar Cells

    International Nuclear Information System (INIS)

    Lee, Woojin; Kang, Suji; Hwang, Taehyun; Kim, Kunsu; Woo, Hyungsub; Lee, Byungho; Kim, Jaewon; Kim, Jinhyun; Park, Byungwoo

    2015-01-01

    Highlights: •3-D hierarchically branched ZnO nanowires by a facile synthesis with seed nucleation. •Nanobranching enhances the efficiency by a factor of two compared with the bare QDSC. •Attributed to the increased sensitizer by ∼80% and decreased transmittance by ∼17%. •Optimized nanostructures correlate with the light-harvesting and carrier-collection efficiencies. -- Abstract: An effective way of synthesizing densely-formed branched ZnO-nanowire arrays was developed by a straightforward conversion reaction of ZnS into ZnO. Hierarchically structured ZnO nanowires are utilized for quantum-dot-sensitized solar cells (QDSCs), having resulted in the conversion-efficiency enhancement by a factor of two compared to the bare ZnO nanowires. This is attributed to the increased CdS-quantum-dot sensitizer by ∼80% and decreased diffused transmittance by ∼17%, induced by the densely-formed branched nanowires. The correlations between the branched nanostructures and photovoltaic performances are systematically investigated in terms of light absorption, charge-transfer resistance, and carrier lifetime. This facile and controllable branched nanowire synthesis is anticipated to be applicable to other semiconductor photoanodes for efficient light harvesting and charge collecting properties

  3. Facile Synthesis and High performance of a New Carbazole-Based Hole Transporting Material for Hybrid Perovskite Solar Cells

    KAUST Repository

    Wang, Hong; Sheikh, Arif D.; Feng, Quanyou; Li, Feng; Chen, Yin; Yu, Weili; Alarousu, Erkki; Ma, Chun; Haque, Mohammed; Shi, Dong; Wang, Zhong-Sheng; Mohammed, Omar F.; Bakr, Osman; Wu, Tao

    2015-01-01

    Perovskite solar cells are very promising for practical applications owing to their rapidly rising power conversion efficiency and low cost of solution-based processing. 2,2’,7,7’-tetrakis-(N,N-di-p-methoxyphenylamine) 9,9’-spirobifluorene (Spiro-OMeTAD) is most widely used as hole transporting material (HTM) in perovskite solar cells. However, the tedious synthesis and high cost of Spiro-OMeTAD inhibit its commercial-scale application in the photovoltaic industry. In this article, we report a carbazole-based compound (R01) as a new HTM in efficient perovskite solar cells. R01 is synthesized via a facile route consisting of only two steps from inexpensive commercially available materials. Furthermore, R01 exhibits higher hole mobility and conductivity than the state-of-the-art Spiro-OMeTAD. Perovskite solar cells fabricated with R01 produce a power conversion efficiency of 12.03%, comparable to that obtained in devices using Spiro-OMeTAD in this study. Our findings underscore R01 as a highly promising HTM with high performance, and its facile synthesis and low cost may facilitate the large-scale applications of perovskite solar cells.

  4. Facile synthesis of concentrated gold nanoparticles with low size-distribution in water: temperature and pH controls

    Directory of Open Access Journals (Sweden)

    Li Chunfang

    2011-01-01

    Full Text Available Abstract The citrate reduction method for the synthesis of gold nanoparticles (GNPs has known advantages but usually provides the products with low nanoparticle concentration and limits its application. Herein, we report a facile method to synthesize GNPs from concentrated chloroauric acid (2.5 mM via adding sodium hydroxide and controlling the temperature. It was found that adding a proper amount of sodium hydroxide can produce uniform concentrated GNPs with low size distribution; otherwise, the largely distributed nanoparticles or instable colloids were obtained. The low reaction temperature is helpful to control the nanoparticle formation rate, and uniform GNPs can be obtained in presence of optimized NaOH concentrations. The pH values of the obtained uniform GNPs were found to be very near to neutral, and the pH influence on the particle size distribution may reveal the different formation mechanism of GNPs at high or low pH condition. Moreover, this modified synthesis method can save more than 90% energy in the heating step. Such environmental-friendly synthesis method for gold nanoparticles may have a great potential in large-scale manufacturing for commercial and industrial demand.

  5. Facile synthesis of concentrated gold nanoparticles with low size-distribution in water: temperature and pH controls

    Science.gov (United States)

    Li, Chunfang; Li, Dongxiang; Wan, Gangqiang; Xu, Jie; Hou, Wanguo

    2011-07-01

    The citrate reduction method for the synthesis of gold nanoparticles (GNPs) has known advantages but usually provides the products with low nanoparticle concentration and limits its application. Herein, we report a facile method to synthesize GNPs from concentrated chloroauric acid (2.5 mM) via adding sodium hydroxide and controlling the temperature. It was found that adding a proper amount of sodium hydroxide can produce uniform concentrated GNPs with low size distribution; otherwise, the largely distributed nanoparticles or instable colloids were obtained. The low reaction temperature is helpful to control the nanoparticle formation rate, and uniform GNPs can be obtained in presence of optimized NaOH concentrations. The pH values of the obtained uniform GNPs were found to be very near to neutral, and the pH influence on the particle size distribution may reveal the different formation mechanism of GNPs at high or low pH condition. Moreover, this modified synthesis method can save more than 90% energy in the heating step. Such environmental-friendly synthesis method for gold nanoparticles may have a great potential in large-scale manufacturing for commercial and industrial demand.

  6. Combustion synthesis and optical properties of Oxy-borate phosphors YCa4O(BO3)3:RE3+ (RE = Eu3+, Tb3+) under UV, VUV excitation

    International Nuclear Information System (INIS)

    Ingle, J.T.; Gawande, A.B.; Sonekar, R.P.; Omanwar, S.K.; Wang, Yuhua; Zhao, Lei

    2014-01-01

    Graphical abstract: VUV Photoluminescence of YCa 4 O(BO 3 ) 3 : Eu 3+ and YCa 4 O(BO 3 ) 3 : Tb 3+ for PDPs applications. Highlights: • Inorganic Oxy-borate phosphors YCa 4 O(BO 3 ) 3 :Eu 3+ ,Tb 3+ was synthesized by novel solution combustion synthesis. • This single host produces efficient and intense Red and Green color for display applications. • Good agreement with CIE co-ordinates as prescribes by NTCL, for flat panel, PDP display color. • Synthesized materials were characterized using powder XRD, FE-SEM, UV and VUV Spectophotometer. -- Abstract: The inorganic Oxy-borate host phosphors YCa 4 O(BO 3 ) 3 :RE 3+ (RE = Eu 3+ ,Tb 3+ ) were synthesized by a novel solution combustion technique. The synthesis is based on the exothermic reaction between the fuel (Urea) and Oxidizer (Ammonium nitrate). The heat generated in reaction is use for auto combustion of precursors. The structures of the prepared samples were confirmed by powder XRD technique. The photoluminescence properties of the powder samples were investigated under UV and VUV excitation; “The phosphor YCa 4 O(BO 3 ) 3 :Eu 3+ and YCa 4 O(BO 3 ) 3 :Tb 3+ shows strong absorption in UV and VUV region and exhibits intense red and green emission upon excited by 254 nm UV and 147 nm VUV radiation”

  7. A facile synthesis of phenazine and quinoxaline derivatives using magnesium sulfate heptahydrate as a catalyst

    Directory of Open Access Journals (Sweden)

    BAHADOR KARAMI

    2011-09-01

    Full Text Available Convenient and simple procedures for the synthesis of phenazine and quinoxaline derivatives were developed via a reaction of o-phenylenediamines and 1,2-dicarbonyl compounds. In addition, the synthesis of two new 1,4-benzodiazine derivatives and the catalytic activity of magnesium sulfate heptahydrate (MgSO4·7H2O in the room temperature condensation of o-phenylenediamines and 1,2-dicarbonyl compounds in ethanol as solvent are reported. This method has many appealing attributes, such as excellent yields, short reaction times, and simple work-up procedures.

  8. A Facile Solvothermal Synthesis of Octahedral Fe3O4 Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ooi, Frances; DuChene, Joseph S.; Qiu, Jianqing; Graham, Jeremy O.; Engelhard, Mark H.; Cao, Guixin; Gai, Zheng; Wei, Wei

    2015-06-01

    Magnetic nanoparticles are of great technological interest because they promise numerous potential opportunities in biomedicine and data storage. Although intriguing, these applications require exquisite control over nanostructure morphology in order to appropriately harness their magnetic properties. Most synthesis strategies reported to date are unable to routinely produce anisotropic Fe3O4 nanostructures with appropriate sizes to enable integration into biological systems. Here, we report a simple solvothermal synthesis for obtaining octahedral Fe3O4 nanoparticles with suitable sizes for cellular internalization. Furthermore, these ferromagnetic Fe3O4 octahedrons exhibit substantial saturation magnetization with minimal remanence, suggesting their potential applicability for a host of biomedical applications.

  9. Combustion synthesis of NiO–Ce0.9Gd0.1O1.95 nanocomposite anode and its electrical characteristics of semi-cell configured SOFC assembly

    International Nuclear Information System (INIS)

    Akbari-Fakhrabadi, A.; Avila, Ricardo E.; Carrasco, Hector E.; Ananthakumar, S.; Mangalaraja, R.V.

    2012-01-01

    Highlights: ► Combustion synthesis was followed to prepare NiO–GDC nanocomposite. ► NiO–GDC anode was applied over GDC electrolyte to fabricate a semi-cell. ► Electrical conductivity of the semi-cell was characterized. ► Structure, composition, particle size and morphology of NiO–GDC were studied. - Abstract: NiO–Ce 0.9 Gd 0.1 O 1.95 (NiO–10GDC) nanocomposite anode material was synthesized through combustion technique for possible low temperature solid oxide fuel cells (LT–SOFCs). A low weight loss is seen in the TG/DTA thermogram that indicates the complete combustion of the reactant mixtures. The powder X-ray diffraction patterns showed that the presence of NiO, GDC and Ni crystallite phases in the as combusted product. Upon calcination at 600 °C, the metallic Ni oxidized to NiO. TEM images showed a wide size distribution of fine spherical GDC and large irregularly shaped NiO particles. This NiO–10GDC anode material was applied over GDC electrolyte as a porous thin layer. Using this surface engineered GDC electrolyte a semi-cell (electrode/electrolyte structure) was fabricated. The electrical conductivity of the semi-cell was characterized with respect to temperature.

  10. A facile approach for the synthesis of porous KTiNbO5 catalyst with ...

    Indian Academy of Sciences (India)

    2018-04-06

    Apr 6, 2018 ... School of Chemical Engineering, Anhui University of Science and Technology, Huainan, Anhui 232001, ... HTiNbO5, is widely used as a catalyst in organic reac- ... synthesized using a facile method and applied in the hydro-.

  11. Facile route for the regioselective synthesis of 1,4-disubstituted 1,2,3 ...

    Indian Academy of Sciences (India)

    MITALI CHETIA

    In this work, a green and efficient methodology has been developed for the synthesis of 1,2,3-triazoles ... Electronic supplementary material: The online version of this article (doi:10.1007/s12039-017-1318-y) ... has come out as a sustainable alternative to conven- ..... Moses J E and Moorhouse A D 2007 The growing appli-.

  12. One-pot, Facile Synthesis of Quinoxaline Derivatives from Bis-aryl a ...

    African Journals Online (AJOL)

    NICO

    Bis-aryl a-Hydroxyketones and o-Arenediamines using. KMnO. 4. /CuSO. 4 ... Faculty of Chemistry, Bu-Ali Sina University, Hamedan 65174, Iran. Received 31 ... cent materials,6 organic semiconductors,7 building blocks for the synthesis of ...

  13. A facile soft template synthesis and characterization of PbHAsO4 nanocrystals

    International Nuclear Information System (INIS)

    Xiu Zhiliang; Lue Mengkai; Zhou Guangjun; Gu Feng; Zhang Haiping; Xu Dong; Yuan Duorong

    2004-01-01

    Monoclinic lead hydrogen arsenate (LHA) nanocrystals with different crystallization morphologies and crystallite sizes were prepared successfully by a soft template synthesis method in the presence of sodium dodecylbenzenesulfonate (SDBS) or polyvinylpyrrolidone (PVP). The products were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The possible mechanism of SDBS and PVP in the experiment was briefly illustrated

  14. Facile synthesis of α-hydroxy carboxylic acids from the corresponding α-amino acids

    DEFF Research Database (Denmark)

    Stuhr-Hansen, Nicolai; Padrah, Shahrokh; Strømgaard, Kristian

    2014-01-01

    An effective and improved procedure is developed for the synthesis of α-hydroxy carboxylic acids by treatment of the corresponding protonated α-amino acid with tert-butyl nitrite in 1,4-dioxane-water. The amino moiety must be protonated and located α to a carboxylic acid function in order...

  15. Facile synthesis of benzofurans via copper-catalyzed aerobic oxidative cyclization of phenols and alkynes.

    Science.gov (United States)

    Zeng, Wei; Wu, Wanqing; Jiang, Huanfeng; Huang, Liangbin; Sun, Yadong; Chen, Zhengwang; Li, Xianwei

    2013-07-28

    Regioselective synthesis of polysubstituted benzofurans using a copper catalyst and molecular oxygen from phenols and alkynes in a one-pot procedure has been reported. The transformation consists of a sequential nucleophilic addition of phenols to alkynes and oxidative cyclization. A wide variety of phenols and alkynes can be used in the same manner.

  16. Synthesis of novel precursors of Pfitzinger reaction: A facile one-pot ...

    Indian Academy of Sciences (India)

    strategy to the synthesis of quinoline carboxylic acid derivatives of ... solution of sodium nitrite (0.7g in 2ml water) while ... sodium acetate trihydrate (1.80 g) in methanol (10 ml) ... the aqueous layer was acidified with acetic acid till neu-.

  17. Synthesis of ligand-free CZTS nanoparticles via a facile hot injection route

    DEFF Research Database (Denmark)

    Mirbagheri, Naghmehalsadat; Engberg, Sara Lena Josefin; Crovetto, Andrea

    2016-01-01

    and toxic solvents that otherwise could hinder grain growth and limit the deposition techniques. In addition the synthesis route presented here results in nanoparticles of a large size compared to other ligand-free CZTS nanoparticles, due to the high boiling point of the solvents selected. Large particle...

  18. Combustion physics

    Science.gov (United States)

    Jones, A. R.

    1985-11-01

    Over 90% of our energy comes from combustion. By the year 2000 the figure will still be 80%, even allowing for nuclear and alternative energy sources. There are many familiar examples of combustion use, both domestic and industrial. These range from the Bunsen burner to large flares, from small combustion chambers, such as those in car engines, to industrial furnaces for steel manufacture or the generation of megawatts of electricity. There are also fires and explosions. The bountiful energy release from combustion, however, brings its problems, prominent among which are diminishing fuel resources and pollution. Combustion science is directed towards finding ways of improving efficiency and reducing pollution. One may ask, since combustion is a chemical reaction, why physics is involved: the answer is in three parts. First, chemicals cannot react unless they come together. In most flames the fuel and air are initially separate. The chemical reaction in the gas phase is very fast compared with the rate of mixing. Thus, once the fuel and air are mixed the reaction can be considered to occur instantaneously and fluid mechanics limits the rate of burning. Secondly, thermodynamics and heat transfer determine the thermal properties of the combustion products. Heat transfer also plays a role by preheating the reactants and is essential to extracting useful work. Fluid mechanics is relevant if work is to be performed directly, as in a turbine. Finally, physical methods, including electric probes, acoustics, optics, spectroscopy and pyrometry, are used to examine flames. The article is concerned mainly with how physics is used to improve the efficiency of combustion.

  19. Facile electrochemical synthesis of few layered graphene from discharged battery electrode and its

    Directory of Open Access Journals (Sweden)

    Santosh K. Tiwari

    2017-05-01

    Full Text Available A cost-effective, simple and non-hazardous route for synthesis of few-layered graphene from waste zinc carbon battery (ZCB electrodes via electrochemical expansion (ECE has been reported. In this synthesis, we have electrochemically exfoliated the graphene layers, by intercalating sodium dodecyl benzenesulfonate (SDBS surfactant into graphitic layers at different D.C. voltages with a constant SDBS concentration. The graphene sheets were isolated, purified and characterized by Transmission electron microscopy (TEM, Scanning electron microscopy (SEM, Fourier transform infrared spectrometry (FTIR, X-ray diffraction (XRD, Raman spectrometry, Ultraviolet absorption (UV, Selected area electron diffraction (SAED and Cyclic voltammetry. Best result was obtained at 4.5 V of D.C. A possible mechanism for the intercalation process has been proposed. A promising application of the produced material for supercapacitor application has also been explored in combination with polyaniline.

  20. Facile method for the synthesis of gold nanoparticles using an ion coater

    Science.gov (United States)

    Lee, Seung Han; Jung, Hyun Kyu; Kim, Tae Cheol; Kim, Chang Hee; Shin, Chang Hwan; Yoon, Tae-Sik; Hong, A.-Ra; Jang, Ho Seong; Kim, Dong Hun

    2018-03-01

    Herein we report a metal nanoparticle synthesis method based on a physical vapor deposition process instead of the conventional wet process of chemical reactions in liquids. A narrow size distribution of synthesized gold nanoparticles was obtained using an ion coater on glycerin at low vapor pressure. The nanoparticle size could be modulated by controlling the sputtering conditions especially the discharge current. Due to the formation of gold nanoparticles, a surface plasmon resonance peak appeared at ∼530 nm in the absorption spectrum. The surface plasmon resonance peak exhibited red-shift with increasing size of the gold nanoparticles. Our results provide a simple, environmental friendly method for the synthesis of metal nanoparticles by combine low-cost deposition apparatus and a liquid medium, which is free from toxic reagents.

  1. Facile and green synthesis of highly stable L-cysteine functionalized copper nanoparticles

    Science.gov (United States)

    Kumar, Nikhil; Upadhyay, Lata Sheo Bachan

    2016-11-01

    A simple eco-friendly method for L-cysteine capped copper nanoparticles (CCNPs) synthesis in aqueous solution has been developed. Glucose and L-cysteine were used as reducing agent and capping/functionalizing agent, respectively. Different parameters such as capping agent concentration, pH, reaction temperature, and reducing agent concentration were optimized during the synthesis. The L-cysteine capped copper nanoparticle were characterized by ultraviolet-visible spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, Particle size and zeta potential analyser, and high resolution transmission electron microscopy. Spherical shaped cysteine functionalized/capped copper nanoparticles with an average size of 40 nm were found to be highly stable at room temperature (RT) for a period of 1 month

  2. Facile synthesis of biocompatible gold nanoparticles with organosilicone-coated surface properties

    Energy Technology Data Exchange (ETDEWEB)

    Xia Lijin; Yi Sijia; Lenaghan, Scott C.; Zhang Mingjun, E-mail: mjzhang@utk.edu [University of Tennessee, Department of Mechanical, Aerospace and Biomedical Engineering (United States)

    2012-07-15

    In this study, a simple method for one-step synthesis of gold nanoparticles has been developed using an organosilicone surfactant, Silwet L-77, as both a reducing and capping agent. Synthesis of gold nanoparticles using this method is rapid and can be conducted conveniently at ambient temperature. Further refinement of the method, through the addition of sodium hydroxide and/or silver nitrate, allowed fine control over the size of spherical nanoparticles produced. Coated on the surface with organosilicone, the as-prepared gold nanoparticles were biocompatible and stable over the pH range from 5 to 12, and have been proven effective at transportation into MC3T3 osteoblast cells. The proposed method is simple, fast, and can produce size-controlled gold nanoparticles with unique surface properties for biomedical applications.

  3. Facile synthesis of biocompatible gold nanoparticles with organosilicone-coated surface properties

    International Nuclear Information System (INIS)

    Xia Lijin; Yi Sijia; Lenaghan, Scott C.; Zhang Mingjun

    2012-01-01

    In this study, a simple method for one-step synthesis of gold nanoparticles has been developed using an organosilicone surfactant, Silwet L-77, as both a reducing and capping agent. Synthesis of gold nanoparticles using this method is rapid and can be conducted conveniently at ambient temperature. Further refinement of the method, through the addition of sodium hydroxide and/or silver nitrate, allowed fine control over the size of spherical nanoparticles produced. Coated on the surface with organosilicone, the as-prepared gold nanoparticles were biocompatible and stable over the pH range from 5 to 12, and have been proven effective at transportation into MC3T3 osteoblast cells. The proposed method is simple, fast, and can produce size-controlled gold nanoparticles with unique surface properties for biomedical applications.

  4. Facile synthesis of biocompatible gold nanoparticles with organosilicone-coated surface properties

    Science.gov (United States)

    Xia, Lijin; Yi, Sijia; Lenaghan, Scott C.; Zhang, Mingjun

    2012-07-01

    In this study, a simple method for one-step synthesis of gold nanoparticles has been developed using an organosilicone surfactant, Silwet L-77, as both a reducing and capping agent. Synthesis of gold nanoparticles using this method is rapid and can be conducted conveniently at ambient temperature. Further refinement of the method, through the addition of sodium hydroxide and/or silver nitrate, allowed fine control over the size of spherical nanoparticles produced. Coated on the surface with organosilicone, the as-prepared gold nanoparticles were biocompatible and stable over the pH range from 5 to 12, and have been proven effective at transportation into MC3T3 osteoblast cells. The proposed method is simple, fast, and can produce size-controlled gold nanoparticles with unique surface properties for biomedical applications.

  5. Facile solid-state synthesis of oxidation-resistant metal nanoparticles at ambient conditions

    Science.gov (United States)

    Lee, Kyu Hyung; Jung, Hyuk Joon; Lee, Ju Hee; Kim, Kyungtae; Lee, Byeongno; Nam, Dohyun; Kim, Chung Man; Jung, Myung-Hwa; Hur, Nam Hwi

    2018-05-01

    A simple and scalable method for the synthesis of metal nanoparticles in the solid-state was developed, which can produce nanoparticles in the absence of solvents. Nanoparticles of coinage metals were synthesized by grinding solid hydrazine and the metal precursors in their acetates and oxides at 25 °C. The silver and gold acetates converted completely within 6 min into Ag and Au nanoparticles, respectively, while complete conversion of the copper acetate to the Cu sub-micrometer particles took about 2 h. Metal oxide precursors were also converted into metal nanoparticles by grinding alone. The resulting particles exhibit distinctive crystalline lattice fringes, indicating the formation of highly crystalline phases. The Cu sub-micrometer particles are better resistant to oxidation and exhibit higher conductivity compared to conventional Cu nanoparticles. This solid-state method was also applied for the synthesis of platinum group metals and intermetallic Cu3Au, which can be further extended to synthesize other metal nanoparticles.

  6. A facile regioselective synthesis of novel spiroacenaphthene pyrroloisoquinolines through 1,3-dipolar cycloaddition reactions

    International Nuclear Information System (INIS)

    Sarrafi, Yaghoub; Asghari, Asieh; Sadatshahabi, Marzieh; Hamzehloueian, Mahshid; Alimohammadi, Kamal

    2013-01-01

    An efficient one-pot three-component procedure for the synthesis of novel spiroacenaphthene pyrroloisoquinolines with high regioselectivity is described. These compounds were prepared from 1,3-dipolar cycloaddition of an azomethine ylide generated from acenaphthenequinone and 1,2,3,4-tetrahydroisoquinoline via [1,5]-H shift, with chalcone and nitrostyrene derivatives as dipolarophiles. The structure and stereochemistry of the cycloadducts have been established by single crystal X-ray structure and spectroscopic techniques. (author)

  7. Facile synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters.

    Science.gov (United States)

    Miura, Tomoya; Funakoshi, Yuuta; Fujimoto, Yoshikazu; Nakahashi, Junki; Murakami, Masahiro

    2015-05-15

    A sequential procedure for the synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters is reported. A copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes with sulfonyl azides affords 1-sulfonyl-1,2,3-triazoles, which then react with thionoesters in the presence of a rhodium(II) catalyst. The resulting 3-sulfonyl-4-thiazolines subsequently aromatize into the corresponding 2,5-disubstituted thiazoles by elimination of the sulfonyl group.

  8. A facile regioselective synthesis of novel spiroacenaphthene pyrroloisoquinolines through 1,3-dipolar cycloaddition reactions

    Energy Technology Data Exchange (ETDEWEB)

    Sarrafi, Yaghoub; Asghari, Asieh; Sadatshahabi, Marzieh, E-mail: ysarrafi@umz.ac.ir [Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran (Iran, Islamic Republic of); Hamzehloueian, Mahshid [Department of Chemistry, Jouybar Branch, Islamic Azad University, Jouybar (Iran, Islamic Republic of); Alimohammadi, Kamal [Department of Chemistry, Dr. Shariati Branch, University of Farhangian, Sari (Iran, Islamic Republic of)

    2013-12-01

    An efficient one-pot three-component procedure for the synthesis of novel spiroacenaphthene pyrroloisoquinolines with high regioselectivity is described. These compounds were prepared from 1,3-dipolar cycloaddition of an azomethine ylide generated from acenaphthenequinone and 1,2,3,4-tetrahydroisoquinoline via [1,5]-H shift, with chalcone and nitrostyrene derivatives as dipolarophiles. The structure and stereochemistry of the cycloadducts have been established by single crystal X-ray structure and spectroscopic techniques. (author)

  9. A facile route to controlled synthesis of Co3O4 nanoparticles and their environmental catalytic properties

    International Nuclear Information System (INIS)

    Dong Yuming; He Kun; Yin Lin; Zhang Aimin

    2007-01-01

    Using ammonia and Co(CH 3 COO) 2 ·4H 2 O as starting materials, a facile and surfactant-free route to controlled synthesis of Co 3 O 4 nanoparticles was proposed. Co 3 O 4 nanoparticles with average sizes of 3.5, 6, 11, 19 and 70 nm were obtained through adjusting the ethanol amount in the solvent (the ratio of ethanol to water) or the concentration of raw materials. In this process, the presence of enough O 2 was crucial for the formation of pure Co 3 O 4 phase. The environmental catalytic properties of as-obtained Co 3 O 4 nanoparticles were investigated. The results indicated their remarkable catalysis for ozonation degradation of phenol, which denoted a promising application as catalyst in waste-water treatment

  10. Facile and solvent-free routes for the synthesis of size-controllable Fe3O4 nanoparticles

    International Nuclear Information System (INIS)

    Ngo, Thanh Hieu; Tran, Dai Lam; Do, Hung Manh; Le, Van Hong; Nguyen, Xuan Phuc; Tran, Vinh Hoang

    2010-01-01

    Magnetite nanoparticles are one of the most important materials that are widely used in both medically diagnostic and therapeutic research. In this paper, we present some facile and non-toxic synthetic approaches for size-controllable preparations of magnetite nanoparticles, which are appropriate for biomedical applications, namely (i) co-precipitation; (ii) reduction–precipitation and (iii) oxidation–precipitation. Magnetic characterizations of the obtained nanoparticles have been studied and discussed. The oxidation precipitation route was chosen for investigation of the dependence of kinetic driven activation energy and that of coercive force on particle size (and temperature) during the course of the reaction. The structural–magnetic behavior was also correlated. Being solvent and surfactant-free, these methods are advantageous for synthesis and further functionalization towards biomedical applications

  11. A facile single injection Hydrothermal method for the synthesis of thiol capped CdTe Quantum dots as light harvesters

    Energy Technology Data Exchange (ETDEWEB)

    Jai Kumar, B.; Sumanth Kumar, D.; Mahesh, H.M., E-mail: hm_mahesh@rediffmail.com

    2016-10-15

    A facile, Single Injection Hydrothermal (SIH) method has been developed to synthesize high quality 3-Mercaptopropionic Acid (MPA) stabilized aqueous CdTe QDs, entirely in ambient environment. The synthesis protocol eliminates the use of inert atmosphere for reducing elemental Tellurium powder to Te precursor avoiding the oxidation of Te powder. The XRD result revealed that the synthesized QDs are in cubic zincblende type crystalline structure, without signature of Te oxidation. FTIR spectra have confirmed the attachment of short chained organic compound MPA to the surface of QDs by covalent bond. The Quantum confinement effect was clearly evident by shift in Longitudinal Optic (LO) peak of Raman spectra and absorption peak wavelength with respect to bulk CdTe materials. The optical direct band gap energy of CdTe QDs is between 3.63 eV to 1.96 eV and QDs size below 6 nm, confirm the QDs are well under strong Quantum confinement regime. Also, photoluminescence spectra depict a stable and high luminescence emission from green to dark red color. All these results corroborate that the synthesis of CdTe QDs procedure is very advantageous and present a simple, economical and easily up scalable method for large scale production.

  12. Facile synthesis of porous Co3O4 nanoplates for supercapacitor ...

    Indian Academy of Sciences (India)

    Administrator

    Abstract. Porous tricobalt tetraoxide (Co3O4) nanoplates with large aspect ratio have been obtained by annealing Co(OH)2 precursor nanoplates synthesized by a facile reflux method without the need for any template or surfactant. After the heat treatment, the as-obtained phase-pure Co3O4 nanoplates with a well- retained ...

  13. Facile solution synthesis of hexagonal Alq3 nanorods and their field emission properties.

    Science.gov (United States)

    Hu, Jin-Song; Ji, Heng-Xing; Cao, An-Min; Huang, Zheng-Xi; Zhang, Yang; Wan, Li-Jun; Xia, An-Dong; Yu, Da-Peng; Meng, Xiang-Min; Lee, Shuit-Tong

    2007-08-07

    A facile self-assembly growth route assisted by surfactant has been developed to synthesize tris(8-hydroxyquinoline)aluminium (Alq(3)) nanorods with regular hexagonal shape and good crystallinity, which exhibit field-emission characteristics with a very low turn-on field of ca. 3.1 V microm(-1) and a high field-enhancement factor of ca. 1300.

  14. Facile Synthesis of Gold Nanorice Enclosed by High- Index Facets and Its Application for CO Oxidation

    International Nuclear Information System (INIS)

    Zheng, Y.; Tao, J.; Liu, H.; Zeng, J.; Yu, T.; Ma, Y.; Moran, C.; Wu, L.; Zhu, Y.; Liu, J.; Xia, Y.

    2011-01-01

    A facile method for generating Au nanorice enclosed by high-index facets in high purity. The nanorice shows much higher catalytic activity for CO oxidation than multiply twinned particles of Au enclosed by {111} facets at temperatures below 300 C.

  15. Vulnerability Assessments and Resilience Planning at Federal Facilities. Preliminary Synthesis of Project

    Energy Technology Data Exchange (ETDEWEB)

    Moss, R. H. [Pacific Northwest National Lab. (PNNL)/Univ. of Maryland, College Park, MD (United States). Joint Global Change Research Inst.; Blohm, A. J. [Univ. of Maryland, College Park, MD (United States); Delgado, A. [Pacific Northwest National Lab. (PNNL)/Univ. of Maryland, College Park, MD (United States). Joint Global Change Research Inst.; Henriques, J. J. [James Madison Univ., Harrisonburg, VA (United States); Malone, E L. [Pacific Northwest National Lab. (PNNL)/Univ. of Maryland, College Park, MD (United States). Joint Global Change Research Inst.

    2015-08-15

    U.S. government agencies are now directed to assess the vulnerability of their operations and facilities to climate change and to develop adaptation plans to increase their resilience. Specific guidance on methods is still evolving based on the many different available frameworks. Agencies have been experimenting with these frameworks and approaches. This technical paper synthesizes lessons and insights from a series of research case studies conducted by the investigators at facilities of the U.S. Department of Energy and the Department of Defense. The purpose of the paper is to solicit comments and feedback from interested program managers and analysts before final conclusions are published. The paper describes the characteristics of a systematic process for prioritizing needs for adaptation planning at individual facilities and examines requirements and methods needed. It then suggests a framework of steps for vulnerability assessments at Federal facilities and elaborates on three sets of methods required for assessments, regardless of the detailed framework used. In a concluding section, the paper suggests a roadmap to further develop methods to support agencies in preparing for climate change. The case studies point to several preliminary conclusions; (1) Vulnerability assessments are needed to translate potential changes in climate exposure to estimates of impacts and evaluation of their significance for operations and mission attainment, in other words into information that is related to and useful in ongoing planning, management, and decision-making processes; (2) To increase the relevance and utility of vulnerability assessments to site personnel, the assessment process needs to emphasize the characteristics of the site infrastructure, not just climate change; (3) A multi-tiered framework that includes screening, vulnerability assessments at the most vulnerable installations, and adaptation design will efficiently target high-risk sites and infrastructure

  16. A divergent [5+2] cascade approach to bicyclo[3.2.1]octanes: facile synthesis of ent-kaurene and cedrene-type skeletons.

    Science.gov (United States)

    He, Chi; Bai, Zengbing; Hu, Jialei; Wang, Bingnan; Xie, Hujun; Yu, Lei; Ding, Hanfeng

    2017-07-25

    A solvent-dependent oxidative dearomatization-induced divergent [5+2] cascade approach to bicyclo[3.2.1]octanes was described. This novel protocol enables a facile synthesis of a series of diversely functionalized ent-kaurene and cedrene-type skeletons in good yields and excellent diastereoselectivities.

  17. Facile synthesis of B-type carbonated nanoapatite with tailored microstructure

    Energy Technology Data Exchange (ETDEWEB)

    Gualtieri, Magdalena Lassinantti, E-mail: magdalena.gualtieri@unimore.it [Dipartimento Ingegneria “Enzo Ferrari”, Università degli studi di Modena e Reggio Emilia, I-41125 Modena (Italy); Romagnoli, Marcello, E-mail: marcello.romagnoli@unimore.it [Dipartimento Ingegneria “Enzo Ferrari”, Università degli studi di Modena e Reggio Emilia, I-41125 Modena (Italy); Hanuskova, Miriam, E-mail: Miriam.hanuskova@unimore.it [Dipartimento Ingegneria “Enzo Ferrari”, Università degli studi di Modena e Reggio Emilia, I-41125 Modena (Italy); Fabbri, Elena, E-mail: Elena.fabbri@unimore.it [Dipartimento Ingegneria “Enzo Ferrari”, Università degli studi di Modena e Reggio Emilia, I-41125 Modena (Italy); Gualtieri, Alessandro F., E-mail: Alessandro.gualtieri@unimore.it [Dipartimento di Scienze Chimiche e Geologiche, Università degli studi di Modena e Reggio Emilia, I-41121 Modena (Italy)

    2014-12-15

    Nanolime and a phosphate-based chelating agent were used to synthesize B-type carbonated apatite. Developed Rietveld refinement strategies allowed one to determine process yield, product crystallinity as well as structural (unit cell) and microstructural (size, strain) parameters. The effect of synthesis temperature (20–60 °C) as well as Ca/P ratio (1.5–2.5) and solid content (10–30 wt%) of the starting batch on these properties were investigated. FTIR, TEM and gas adsorption data provided supporting evidence. The process yield was 42–60 wt% and found to be governed by the Ca/P ratio. The purified products had high specific surface area (107–186 m{sup 2}/g) and crystallinity (76–97%). The unit cell parameters, correlated to the degree of structural carbonate, were sensitive to the Ca/P ratio. Instead, temperature governed the microstructural parameters. Less strained and larger crystals were obtained at higher temperatures. Long-term aging up to 6 months at 20 °C compensated for higher crystal growth kinetics at higher temperature. - Graphical abstract: Controlled synthesis of carbonated apatite at moderate temperatures using nanolime and sodiumhexametaphosphate as starting reagent. - Highlights: • Chemical synthesis of nano-sized apatite with tailored microstructure was performed. • Colloidal Ca(OH){sub 2} and a phosphorus-based chelating agents were used as reagents. • The method is simple and reproducible which facilitate industrial process scale-up. • Rietveld refinement strategies for product characterization were developed. • Rietveld analyses provided yield, microstructural and structure information.

  18. Facile synthesis of B-type carbonated nanoapatite with tailored microstructure

    International Nuclear Information System (INIS)

    Gualtieri, Magdalena Lassinantti; Romagnoli, Marcello; Hanuskova, Miriam; Fabbri, Elena; Gualtieri, Alessandro F.

    2014-01-01

    Nanolime and a phosphate-based chelating agent were used to synthesize B-type carbonated apatite. Developed Rietveld refinement strategies allowed one to determine process yield, product crystallinity as well as structural (unit cell) and microstructural (size, strain) parameters. The effect of synthesis temperature (20–60 °C) as well as Ca/P ratio (1.5–2.5) and solid content (10–30 wt%) of the starting batch on these properties were investigated. FTIR, TEM and gas adsorption data provided supporting evidence. The process yield was 42–60 wt% and found to be governed by the Ca/P ratio. The purified products had high specific surface area (107–186 m 2 /g) and crystallinity (76–97%). The unit cell parameters, correlated to the degree of structural carbonate, were sensitive to the Ca/P ratio. Instead, temperature governed the microstructural parameters. Less strained and larger crystals were obtained at higher temperatures. Long-term aging up to 6 months at 20 °C compensated for higher crystal growth kinetics at higher temperature. - Graphical abstract: Controlled synthesis of carbonated apatite at moderate temperatures using nanolime and sodiumhexametaphosphate as starting reagent. - Highlights: • Chemical synthesis of nano-sized apatite with tailored microstructure was performed. • Colloidal Ca(OH) 2 and a phosphorus-based chelating agents were used as reagents. • The method is simple and reproducible which facilitate industrial process scale-up. • Rietveld refinement strategies for product characterization were developed. • Rietveld analyses provided yield, microstructural and structure information

  19. High yield and facile microwave-assisted synthesis of conductive H_2SO_4 doped polyanilines

    International Nuclear Information System (INIS)

    Gizdavic-Nikolaidis, Marija R.; Jevremovic, Milutin M.; Milenkovic, Maja; Allison, Morgan C.; Stanisavljev, Dragomir R.; Bowmaker, Graham A.; Zujovic, Zoran D.

    2016-01-01

    The microwave-assisted synthesis of polyaniline (PANI) was performed using ammonium persulphate (APS) as oxidizing agent in 0.5 M–2.5 M concentration range of aqueous sulphuric acid (H_2SO_4) at 93 W applied microwave power of 10 min duration. The microwave (MW) synthesized PANIs had 3 times higher yield in comparison to PANI samples prepared using a classical method, CS (0 W MW power) at the same temperature for 10 min synthesis duration period. Fourier Transform Infrared (FTIR) and UV–Vis spectroscopies confirmed the formation of PANI structure in all products. The influence of H_2SO_4 acid dopant on the spin concentration of MW and CS H_2SO_4 doped PANI samples were examined by EPR spectroscopy, while the morphological characteristics were investigated by using scanning electron microscopy (SEM). XRD results showed amorphous phases in both MW and CS H_2SO_4 doped PANI samples. Conductivity measurements revealed ∼1.5 times higher conductivity values for MW H_2SO_4 doped PANI samples in comparison with PANI samples prepared by the CS method under same condition. The influence of sulfate anion in comparison to chloride anion as a dopant on morphological, dopant levels and conductivity properties of MW PANI samples were also investigated. - Highlights: • Nanoporous microwave synthesized doped polyanilines as chemical sensor material. • Morphology and physical properties of polyanilines depend on acid concentration. • Spin concentration is determined by the nature of the polyaniline synthesis.

  20. Facile and green synthesis of mesoporous Co3O4 nanocubes and their applications for supercapacitors

    Science.gov (United States)

    Liu, Xiangmei; Long, Qing; Jiang, Chunhui; Zhan, Beibei; Li, Chen; Liu, Shujuan; Zhao, Qiang; Huang, Wei; Dong, Xiaochen

    2013-06-01

    Nanostructured Co3O4 materials attracted significant attention due to their exceptional electrochemical (pseudo-capacitive) properties. However, rigorous preparation conditions are needed to control the size (especially nanosize), morphology and size distribution of the products obtained by conventional methods. Herein, we describe a novel one step shape-controlled synthesis of uniform Co3O4 nanocubes with a size of 50 nm with the existence of mesoporous carbon nanorods (meso-CNRs). In this synthesis process, meso-CNRs not only act as a heat receiver to directly obtain Co3O4 eliminating the high-temperature post-calcination, but also control the morphology of the resulting Co3O4 to form nanocubes with uniform distribution. More strikingly, mesoporous Co3O4 nanocubes are obtained by further thermal treatment. The structure and morphology of the samples were characterized by scanning electron microscopy, transmission electron microscopy and X-ray diffraction. A possible formation mechanism of mesoporous Co3O4 nanocubes is proposed here. Electrochemical tests have revealed that the prepared mesoporous Co3O4 nanocubes demonstrate a remarkable performance in supercapacitor applications due to the porous structure, which endows fast ion and electron transfer.Nanostructured Co3O4 materials attracted significant attention due to their exceptional electrochemical (pseudo-capacitive) properties. However, rigorous preparation conditions are needed to control the size (especially nanosize), morphology and size distribution of the products obtained by conventional methods. Herein, we describe a novel one step shape-controlled synthesis of uniform Co3O4 nanocubes with a size of 50 nm with the existence of mesoporous carbon nanorods (meso-CNRs). In this synthesis process, meso-CNRs not only act as a heat receiver to directly obtain Co3O4 eliminating the high-temperature post-calcination, but also control the morphology of the resulting Co3O4 to form nanocubes with uniform

  1. Facile and efficient synthesis of [{sup 18}F]fluoromisonidazole using novel 2-nitroimidazole derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Kwon, Young-Do; Lim, Seok Tae; Sohn, Myung-Hee; Kim, Hee-Kwon, E-mail: hkkim717@jbnu.ac.kr [Department of Nuclear Medicine, Chonbuk National University Medical School and Hospital, Jeonju (Korea, Republic of); Jung, Yongju [Department of Chemical Engineering, Korea University of Technology and Education, Cheonan (Korea, Republic of)

    2016-07-01

    [{sup 18}F]Fluoromisonidazole ([{sup 18}F]FMISO) is a hypoxia imaging marker utilized in positron emission tomography. Novel FMISO precursors were prepared from a commercially available material, and several reaction factors that affect synthesis of [{sup 18}F]FMISO were examined to achieve a higher fluorination yield. [{sup 18}F]FMISO was obtained from radiosynthesis, followed by the hydrolysis of protecting groups with HCl. New 2-nitroimidazole precursor showed a higher [{sup 18}F]fluorination and a higher synthetic yield. This result provided alternative guidelines for the preparation of hypoxia imaging marker. (author)

  2. Design of generic coal conversion facilities: Production of oxygenates from synthesis gas---A technology review

    Energy Technology Data Exchange (ETDEWEB)

    1991-10-01

    This report concentrates on the production of oxygenates from coal via gasification and indirect liquefaction. At the present the majority of oxygenate synthesis programs are at laboratory scale. Exceptions include commercial and demonstration scale plants for methanol and higher alcohols production, and ethers such as MTBE. Research and development work has concentrated on elucidating the fundamental transport and kinetic limitations governing various reactor configurations. But of equal or greater importance has been investigations into the optimal catalyst composition and process conditions for the production of various oxygenates.

  3. Facile synthesis of ZrO2 powders: Control of morphology

    International Nuclear Information System (INIS)

    Grover, V.; Shukla, R.; Tyagi, A.K.

    2007-01-01

    Tetragonal (t-)ZrO 2 rods and spheres were prepared by simple and time-saving low-temperature synthesis and characterized by X-ray diffraction, Raman spectroscopy and scanning electron microscopy. The morphology of the product can be changed from rods to spheres by changing the reaction conditions slightly. The t-ZrO 2 rods (0.5-0.1 mm approximately) were obtained by topotactic reaction. The work illustrates the utility of Raman spectroscopy as a powerful characterization tool when XRD is not able to conclusively identify the phases

  4. A Facile and Mild Synthesis of Trisubstituted Allylic Sulfones from Morita-Baylis-Hillman Carbonates

    Directory of Open Access Journals (Sweden)

    Lin Jiang

    2015-05-01

    Full Text Available An efficient and catalyst-free synthesis of trisubstituted allylic sulfones through an allylic sulfonylation reaction of Morita-Baylis-Hillman (MBH carbonates with sodium sulfinates has been developed. Under the optimized reaction conditions, a series of trisubstituted allylic sulfones were rapidly prepared in good to excellent yields (71%–99% with good to high selectivity (Z/E from 79:21 to >99:1. Compared with known synthetic methods, the current protocol features mild reaction temperature, high efficiency and easily available reagents.

  5. A facile and mild synthesis of trisubstituted allylic sulfones from Morita-Baylis-Hillman carbonates.

    Science.gov (United States)

    Jiang, Lin; Li, Yong-Gen; Zhou, Jiang-Feng; Chuan, Yong-Ming; Li, Hong-Li; Yuan, Ming-Long

    2015-05-07

    An efficient and catalyst-free synthesis of trisubstituted allylic sulfones through an allylic sulfonylation reaction of Morita-Baylis-Hillman (MBH) carbonates with sodium sulfinates has been developed. Under the optimized reaction conditions, a series of trisubstituted allylic sulfones were rapidly prepared in good to excellent yields (71%-99%) with good to high selectivity (Z/E from 79:21 to >99:1). Compared with known synthetic methods, the current protocol features mild reaction temperature, high efficiency and easily available reagents.

  6. Effect of particle- and specimen-level transport on product state in compacted-powder combustion synthesis and thermal debinding of polymers from molded powders

    Science.gov (United States)

    Oliveira, Amir Antonio Martins

    The existence of large gradients within particles and fast temporal variations in the temperature and species concentration prevents the use of asymptotic approximations for the closure of the volume-averaged, specimen-level formulations. In this case a solution of the particle-level transport problem is needed to complement the specimen-level volume-averaged equations. Here, the use of combined specimen-level and particle-level models for transport in reactive porous media is demonstrated with two examples. For the gasless compacted-powder combustion synthesis, a three-scale model is developed. The specimen-level model is based on the volume-averaged equations for species and temperature. Local thermal equilibrium is assumed and the macroscopic mass diffusion and convection fluxes are neglected. The particle-level model accounts for the interparticle diffusion (i.e., the liquid migration from liquid-rich to liquid-lean regions) and the intraparticle diffusion (i.e., the species mass diffusion within the product layer formed at the surface of the high melting temperature component). It is found that the interparticle diffusion controls the extent of conversion to the final product, the maximum temperature, and to a smaller degree the propagation velocity. The intraparticle diffusion controls the propagation velocity and to a smaller degree the maximum temperature. The initial stages of thermal degradation of EVA from molded specimens is modeled using volume-averaged equations for the species and empirical models for the kinetics of the thermal degradation, the vapor-liquid equilibrium, and the diffusion coefficient of acetic acid in the molten polymer. It is assumed that a bubble forms when the partial pressure of acetic acid exceeds the external ambient pressure. It is found that the removal of acetic acid is characterized by two regimes, a pre-charge dominated regime and a generation dominated regime. For the development of an optimum debinding schedule, the

  7. Facile synthesis of highly active PdAu nanowire networks as self-supported electrocatalyst for ethanol electrooxidation.

    Science.gov (United States)

    Hong, Wei; Wang, Jin; Wang, Erkang

    2014-06-25

    In recent years, direct ethanol fuel cells (DEFCs) are attracting increasing attention owing to their wide applications. However, a significant challenge in the development of DEFC technology is the urgent need for highly active anode catalysts for the ethanol oxidation reaction. In this work, a facile and reproducible method for the high-yield synthesis of PdAu nanowire networks is demonstrated. The whole synthetic process is very simple, just mixing Na2PdCl4, HAuCl4, and KBr in an aqueous solution and using polyvinylpyrrolidone as a protective reagent while sodium borohydride as a reductant. The whole synthetic process can be simply performed at room temperature and completed in 30 min, which can greatly simplify the synthetic process and lower the preparation cost. Electrochemical catalytic measurement results prove that the as-prepared catalysts exhibit dramatically enhanced electrocatalytic activity for ethanol electrooxidation in alkaline solution. The facile synthetic process and excellent catalytic performance of the as-prepared catalysts demonstrate that they can be used as a promising catalyst for DEFCs.

  8. Facile synthesis of bacitracin-templated palladium nanoparticles with superior electrocatalytic activity

    Science.gov (United States)

    Li, Yanji; Wang, Zi; Li, Xiaoling; Yin, Tian; Bian, Kexin; Gao, Faming; Gao, Dawei

    2017-02-01

    Palladium nanomaterials have attracted great attention on the development of electrocatalysts for fuel cells. Herein, we depicted a novel strategy in the synthesis of palladium nanoparticles with superior electrocatalytic activity. The new approach, based on the self-assembly of bacitracin biotemplate and palladium salt for the preparation of bacitracin-palladium nanoparticles (Bac-PdNPs), was simple, low-cost, and green. The complex, composed by a series of spherical Bac-PdNPs with a diameter of 70 nm, exhibited a chain-liked morphology in TEM and a face-centered cubic crystal structure in X-Ray diffraction and selected area electron diffraction. The palladium nanoparticles were mono-dispersed and stable in aqueous solution as shown in TEM and zeta potential. Most importantly, compared to the commercial palladium on carbon (Pd/C) catalyst (8.02 m2 g-1), the Bac-PdNPs showed a larger electrochemically active surface area (47.57 m2 g-1), which endowed the products an excellent electrocatalytic activity for ethanol oxidation in alkaline medium. The strategy in synthesis of Bac-PdNPs via biotemplate approach might light up new ideas in anode catalysts for direct ethanol fuel cells.

  9. Facile synthesis of “green” gold nanocrystals using cynarin in an aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Katircioğlu, Zeynep; Şakalak, Hüseyin [Department of Metallurgical and Materials Engineering, Selcuk University, Konya 42075 (Turkey); Nanobiotechnology Laboratory, Advanced Technology Research and Application Center, Selcuk University, Konya 42075 (Turkey); Ulaşan, Mehmet [Nanobiotechnology Laboratory, Advanced Technology Research and Application Center, Selcuk University, Konya 42075 (Turkey); Department of Chemistry, Selcuk University, Konya 42075 (Turkey); Gören, Ahmet Ceyhan, E-mail: ahmetceyhan.goren@tubitak.gov.tr [TÜBİTAK UME, Chemistry Group, Organic Chemistry Laboratories, 41470 Gebze, Kocaeli (Turkey); Yavuz, Mustafa Selman, E-mail: selmanyavuz@selcuk.edu.tr [Department of Metallurgical and Materials Engineering, Selcuk University, Konya 42075 (Turkey); Nanobiotechnology Laboratory, Advanced Technology Research and Application Center, Selcuk University, Konya 42075 (Turkey)

    2014-11-01

    Highlights: • The first time a remarkably simple, versatile, environmentally friendly, one-pot and biogenic fabrication and aqueous synthesis of monodisperse gold nanoparticles by using cynarin. • Cynarin as a reductant and capping agent. • Exclusion of extra reducing agents or reductant. • Fabrication of Pd and Ag nanoparticles using cynarin in aqueous media. - Abstract: Herein we describe a water-based protocol that generates Au nanoparticles (AuNPs) by mixing aqueous solutions of HAuCl4 and cynarin (a natural product extract from artichoke leaf). Based on the observations from {sup 1}H NMR spectrum of AuNPs, a polyol oxidation mechanism by metal ions which eventually results in AuNPs formation, is proposed. Basically, the aromatic alcohol groups (1,2-benzenediol) of cynarin are oxidized to α-hydroxy ketone intermediate product, and then further oxidized to the vicinal diketone final product while the Au{sup 3+} ions are reduced to its atomic form (Au{sup 0}) which leads the generation of Au nanoparticles. This new protocol has also been employed to prepare multiply twinned Pd nanoparticles and Ag cubical aggregates. Due to exclusion of organic solvent, surfactant, or stabilizer for all these synthesis, this protocol may provide a simple, versatile, and environmentally benign route to fabricate noble-metal nanoparticles having various compositions and morphologies.

  10. Facile synthesis of “green” gold nanocrystals using cynarin in an aqueous solution

    International Nuclear Information System (INIS)

    Katircioğlu, Zeynep; Şakalak, Hüseyin; Ulaşan, Mehmet; Gören, Ahmet Ceyhan; Yavuz, Mustafa Selman

    2014-01-01

    Highlights: • The first time a remarkably simple, versatile, environmentally friendly, one-pot and biogenic fabrication and aqueous synthesis of monodisperse gold nanoparticles by using cynarin. • Cynarin as a reductant and capping agent. • Exclusion of extra reducing agents or reductant. • Fabrication of Pd and Ag nanoparticles using cynarin in aqueous media. - Abstract: Herein we describe a water-based protocol that generates Au nanoparticles (AuNPs) by mixing aqueous solutions of HAuCl4 and cynarin (a natural product extract from artichoke leaf). Based on the observations from 1 H NMR spectrum of AuNPs, a polyol oxidation mechanism by metal ions which eventually results in AuNPs formation, is proposed. Basically, the aromatic alcohol groups (1,2-benzenediol) of cynarin are oxidized to α-hydroxy ketone intermediate product, and then further oxidized to the vicinal diketone final product while the Au 3+ ions are reduced to its atomic form (Au 0 ) which leads the generation of Au nanoparticles. This new protocol has also been employed to prepare multiply twinned Pd nanoparticles and Ag cubical aggregates. Due to exclusion of organic solvent, surfactant, or stabilizer for all these synthesis, this protocol may provide a simple, versatile, and environmentally benign route to fabricate noble-metal nanoparticles having various compositions and morphologies

  11. Facile one-pot synthesis of gold and silver nanocatalysts using edible coconut oil

    Science.gov (United States)

    Meena Kumari, M.; Philip, Daizy

    2013-07-01

    The use of edible oil for the synthesis of metal nanoparticles by wet chemical method is reported for the first time. The paper presents an environmentally benign bottom up approach for the synthesis of gold and silver nanoparticles using edible coconut oil at 373 K. The formation of silver nanoparticles is signaled by the brownish yellow color and that of gold nanoparticles by the purple color. Fine control over the nanoparticle size and shape from triangular to nearly spherical is achieved by varying the quantity of coconut oil. The nanoparticles have been characterized by UV-Visible, Transmission Electron Microscopy and X-ray Diffraction. The chemical interaction of capping agents with metal nanoparticles is manifested using Fourier Transform Infrared Spectroscopy. The stable and crystalline nanoparticles obtained using this simple method show remarkable size-dependent catalytic activity in the reduction of the cationic dye methylene blue (MB) to leuco methylene blue (LMB). The first order rate constants calculated uphold the size dependent catalytic activity of the synthesized nanoparticles.

  12. A facile and fast approach for the synthesis of doped nanoparticles using a microfluidic device

    International Nuclear Information System (INIS)

    Singh, Akanksha; Limaye, Mukta; Singh, Shashi; Kulkarni, Sulabha; Lalla, Niranjan Prasad; Malek, Chantal Khan

    2008-01-01

    The microfluidic approach emerges as a new and promising technology for the synthesis of nanomaterials. A microreactor allows a variety of reaction conditions to be quickly scanned without consuming large amounts of raw material. In this study, we investigated the synthesis of water soluble 1-thioglycerol-capped Mn-doped ZnS nanocrystalline semiconductor nanoparticles (TG-capped ZnS:Mn) via a microfluidic approach. This is the first report for the successful doping of Mn in a ZnS semiconductor at room temperature as well as at 80 deg. C using a microreactor. Transmission electron microscopy and x-ray diffraction analysis show that the average particle size of Mn-doped ZnS nanoparticles is ∼3.0 nm with a zinc-blende structure. Photoluminescence, x-ray photoelectron spectroscopy, atomic absorption spectroscopy and electron paramagnetic resonance studies were carried out to confirm that the Mn 2+ dopants are present in the ZnS nanoparticles

  13. Facile synthesis of graphene oxide @ mesoporous carbon hybrid nanocomposites for lithium sulfur battery

    International Nuclear Information System (INIS)

    Bao, Weizhai; Zhang, Zhian; Chen, Wei; Zhou, Chengkun; Lai, Yanqing; Li, Jie

    2014-01-01

    Graphical abstract: - Highlights: • A novel design and synthesis of GO@Meso-C using GO@MOF-5 as precursor. • GO@Meso-C hybrid material as a host material was applied for sulfur cathode. • Electrochemical performances were improved in sulfur cathode using Go@Meso-C. - Abstract: We present a design and synthesis of a hierarchical architecture of graphene oxide @ mesoporous carbon (GO@Meso-C) using graphene oxide @ metal-organic framework hybrid materials (GO@MOF-5) as both the template and precursor. Active sulfur is encapsulated into the GO@Meso-C matrix prepared via carbonize GO@MOF-5 polyhedrons for high performance lithium sulfur battery. The initial and 100th cycle discharge capacity of GO@Meso-C/S sulfur cathode are as high as 1122 mAh g −1 and 820 mAh g −1 at a current rate of 0.2 C. The remarkably high special capacity and capacity retention rate indicate that the GO@Meso-C is a promising host material for the sulfur cathode in the lithium sulfur battery applications

  14. Space Station Freedom combustion research

    Science.gov (United States)

    Faeth, G. M.

    1992-01-01

    Extended operations in microgravity, on board spacecraft like Space Station Freedom, provide both unusual opportunities and unusual challenges for combustion science. On the one hand, eliminating the intrusion of buoyancy provides a valuable new perspective for fundamental studies of combustion phenomena. On the other hand, however, the absence of buoyancy creates new hazards of fires and explosions that must be understood to assure safe manned space activities. These considerations - and the relevance of combustion science to problems of pollutants, energy utilization, waste incineration, power and propulsion systems, and fire and explosion hazards, among others - provide strong motivation for microgravity combustion research. The intrusion of buoyancy is a greater impediment to fundamental combustion studies than to most other areas of science. Combustion intrinsically heats gases with the resulting buoyant motion at normal gravity either preventing or vastly complicating measurements. Perversely, this limitation is most evident for fundamental laboratory experiments; few practical combustion phenomena are significantly affected by buoyancy. Thus, we have never observed the most fundamental combustion phenomena - laminar premixed and diffusion flames, heterogeneous flames of particles and surfaces, low-speed turbulent flames, etc. - without substantial buoyant disturbances. This precludes rational merging of theory, where buoyancy is of little interest, and experiments, that always are contaminated by buoyancy, which is the traditional path for developing most areas of science. The current microgravity combustion program seeks to rectify this deficiency using both ground-based and space-based facilities, with experiments involving space-based facilities including: laminar premixed flames, soot processes in laminar jet diffusion flames, structure of laminar and turbulent jet diffusion flames, solid surface combustion, one-dimensional smoldering, ignition and flame

  15. Diatomite-immobilized BiOI hybrid photocatalyst: Facile deposition synthesis and enhanced photocatalytic activity

    International Nuclear Information System (INIS)

    Li, Baoying; Huang, Hongwei; Guo, Yuxi; Zhang, Yihe

    2015-01-01

    Graphical abstract: - Highlights: • A novel diatomite-immobilized BiOI hybrid photocatalyst has been prepared by a facile one-step deposition process for the first time. • The diatomite-immobilized BiOI hybrid photocatalyst exhibits much better photocatalytic performance. • This enhancement should be attributed to that diatomite can play as an excellent carrier platform to increase the reactive sites and promote the separation of photogenerated electron–hole pairs. • This work shed new light on facile fabrication of novel composite photocatalyst based on natural mineral. - Abstract: A novel diatomite-immobilized BiOI hybrid photocatalyst has been prepared by a facile one-step deposition process for the first time. The structure, morphology and optical property of the products were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and UV–vis diffuse reflectance spectroscopy (DRS). The photocatalytic performance of the as-prepared BiOI/diatomite photocatalysts was studied by photodegradation of Rhodamine B (RhB) and methylene blue (MB) and monitoring photocurrent generation under visible light (λ > 420 nm). The results revealed that BiOI/diatomite composites exhibit enhanced photocatalytic activity compared to the pristine BiOI sample. This enhancement should be attributed to that diatomite can play as an excellent carrier platform to increase the reactive sites and promote the separation of photogenerated electron–hole pairs. In addition, the corresponding photocatalytic mechanism was proposed based on the active species trapping experiments. This work shed new light on facile fabrication of novel composite photocatalyst based on natural mineral.

  16. Antibiotic Prescribing in Long-Term Care Facilities: A Meta-synthesis of Qualitative Research

    OpenAIRE

    Fleming, Aoife; Bradley, Colin; Cullinan, Shane; Byrne, Stephen

    2015-01-01

    Objectives The objective of this review was to synthesize the findings of qualitative studies investigating the factors influencing antibiotic prescribing in long-term care facilities (LTCFs). These findings will inform the development of future antimicrobial stewardship strategies (AMS) in this setting. Methods We searched Embase, PubMed, PsycInfo, Social Science Citations Index and Google Scholar for all qualitative studies investigating health care professionals? views on antibiotic prescr...

  17. Facile one-pot synthesis of porphyrin based porous polymer networks (PPNs) as biomimetic catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Zou, LF; Feng, DW; Liu, TF; Chen, YP; Fordham, S; Yuan, S; Tian, J; Zhou, HC

    2015-01-01

    Stable porphyrin based porous polymer networks, PPN-23 and PPN-24, have been synthesized through a facile one-pot approach by the aromatic substitution reactions of pyrrole and aldehydes. PPN-24(Fe) shows high catalytic efficiency as a biomimetic catalyst in the oxidation reaction of 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) in the presence of H2O2.

  18. Facile and Scalable Synthesis of Monodispersed Spherical Capsules with a Mesoporous Shell

    KAUST Repository

    Qi, Genggeng

    2010-05-11

    Monodispersed HMSs with tunable particle size and shell thickness were successfully synthesized using relatively concentrated polystyrene latex templates and a silica precursor in a weakly basic ethanol/water mixture. The particle size of the capsules can vary from 100 nm to micrometers. These highly engineered monodispersed capsules synthesized by a facile and scalable process may find applications in drug delivery, catalysis, separationm or as biological and chemical microreactors. © 2010 American Chemical Society.

  19. Diatomite-immobilized BiOI hybrid photocatalyst: Facile deposition synthesis and enhanced photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Li, Baoying; Huang, Hongwei, E-mail: hhw@cugb.edu.cn; Guo, Yuxi; Zhang, Yihe, E-mail: zyh@cugb.edu.cn

    2015-10-30

    Graphical abstract: - Highlights: • A novel diatomite-immobilized BiOI hybrid photocatalyst has been prepared by a facile one-step deposition process for the first time. • The diatomite-immobilized BiOI hybrid photocatalyst exhibits much better photocatalytic performance. • This enhancement should be attributed to that diatomite can play as an excellent carrier platform to increase the reactive sites and promote the separation of photogenerated electron–hole pairs. • This work shed new light on facile fabrication of novel composite photocatalyst based on natural mineral. - Abstract: A novel diatomite-immobilized BiOI hybrid photocatalyst has been prepared by a facile one-step deposition process for the first time. The structure, morphology and optical property of the products were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and UV–vis diffuse reflectance spectroscopy (DRS). The photocatalytic performance of the as-prepared BiOI/diatomite photocatalysts was studied by photodegradation of Rhodamine B (RhB) and methylene blue (MB) and monitoring photocurrent generation under visible light (λ > 420 nm). The results revealed that BiOI/diatomite composites exhibit enhanced photocatalytic activity compared to the pristine BiOI sample. This enhancement should be attributed to that diatomite can play as an excellent carrier platform to increase the reactive sites and promote the separation of photogenerated electron–hole pairs. In addition, the corresponding photocatalytic mechanism was proposed based on the active species trapping experiments. This work shed new light on facile fabrication of novel composite photocatalyst based on natural mineral.

  20. LES and RANS modeling of pulverized coal combustion in swirl burner for air and oxy-combustion technologies

    International Nuclear Information System (INIS)

    Warzecha, Piotr; Boguslawski, Andrzej

    2014-01-01

    Combustion of pulverized coal in oxy-combustion technology is one of the effective ways to reduce the emission of greenhouse gases into the atmosphere. The process of transition from conventional combustion in air to the oxy-combustion technology, however, requires a thorough investigations of the phenomena occurring during the combustion process, that can be greatly supported by numerical modeling. The paper presents the results of numerical simulations of pulverized coal combustion process in swirl burner using RANS (Reynolds-averaged Navier–Stokes equations) and LES (large Eddy simulation) methods for turbulent flow. Numerical simulations have been performed for the oxyfuel test facility located at the Institute of Heat and Mass Transfer at RWTH Aachen University. Detailed analysis of the flow field inside the combustion chamber for cold flow and for the flow with combustion using different numerical methods for turbulent flows have been done. Comparison of the air and oxy-coal combustion process for pulverized coal shows significant differences in temperature, especially close to the burner exit. Additionally the influence of the combustion model on the results has been shown for oxy-combustion test case. - Highlights: • Oxy-coal combustion has been modeled for test facility operating at low oxygen ratio. • Coal combustion process has been modeled with simplified combustion models. • Comparison of oxy and air combustion process of pulverized coal has been done. • RANS (Reynolds-averaged Navier–Stokes equations) and LES (large Eddy simulation) results for pulverized coal combustion process have been compared

  1. Biofuels combustion.

    Science.gov (United States)

    Westbrook, Charles K

    2013-01-01

    This review describes major features of current research in renewable fuels derived from plants and from fatty acids. Recent and ongoing fundamental studies of biofuel molecular structure, oxidation reactions, and biofuel chemical properties are reviewed, in addition to combustion applications of biofuels in the major types of engines in which biofuels are used. Biofuels and their combustion are compared with combustion features of conventional petroleum-based fuels. Two main classes of biofuels are described, those consisting of small, primarily alcohol, fuels (particularly ethanol, n-butanol, and iso-pentanol) that are used primarily to replace or supplement gasoline and those derived from fatty acids and used primarily to replace or supplement conventional diesel fuels. Research efforts on so-called second- and third-generation biofuels are discussed briefly.

  2. Ignition and wave processes in combustion of solids

    CERN Document Server

    Rubtsov, Nickolai M; Alymov, Michail I

    2017-01-01

    This book focuses on the application of classical combustion theory to ignition and flame propagation in solid-solid and gas-solid systems. It presents experimental investigations in the areas of local ignition, filtration combustion, self-propagating high temperature synthesis and nanopowders protection. The authors highlight analytical formulas used in different areas of combustion in solids and propose an approach based on classical combustion theory. The book attempts to analyze the basic approaches to understanding of solid-solid and solid - gas combustion presented in contemporary literature in a unified approach based on classical combustion theory. .

  3. Synthesis of Pr0.70Sr0.30MnO3δ and Nd0.70Sr0.30MnO3δ powders by solution-combustion technique

    Directory of Open Access Journals (Sweden)

    Reinaldo Azevedo Vargas

    2011-01-01

    Full Text Available Powders of Pr0.70Sr0.30MnO3δ (PSM and Nd0.70Sr0.30MnO3δ (NSM compositions are being investigated as alternative cathode materials for Intermediate Temperature Solid Oxide Fuel Cells. The compositions were synthesized by a solution-combustion method using metal nitrates and urea as fuel. Combustion synthesis is a highly suitable synthesis route for achieving fine and homogeneous powders at low temperatures. Single phase pseudo-perovskite was obtained by X-ray diffraction after heat treatment of PSM and NSM powders at 900 ºC. The synthesized and milling powders had an average particle size between 0.27 to 0.07 μm. Chemical analyses of the powders calcined was performed by X-ray fluorescence and morphological analysis by scanning electron microscopy. The results were compared with literature values, indicating characteristics adjusted for preparation of ceramic suspensions.

  4. Facile Synthesis and Tensile Behavior of TiO2 One-Dimensional Nanostructures

    Directory of Open Access Journals (Sweden)

    Li Shu-you

    2009-01-01

    Full Text Available Abstract High-yield synthesis of TiO2 one-dimensional (1D nanostructures was realized by a simple annealing of Ni-coated Ti grids in an argon atmosphere at 950 °C and 760 torr. The as-synthesized 1D nanostructures were single crystalline rutile TiO2 with the preferred growth direction close to [210]. The growth of these nanostructures was enhanced by using catalytic materials, higher reaction temperature, and longer reaction time. Nanoscale tensile testing performed on individual 1D nanostructures showed that the nanostructures appeared to fracture in a brittle manner. The measured Young’s modulus and fracture strength are ~56.3 and 1.4 GPa, respectively.

  5. Make and break - Facile synthesis of cocrystals and comprehensive dissolution studies

    Science.gov (United States)

    Batzdorf, L.; Zientek, N.; Rump, D.; Fischer, F.; Maiwald, M.; Emmerling, F.

    2017-04-01

    Mechanochemistry is increasingly used as a 'green alternative' for synthesizing various materials including pharmaceutical cocrystals. Herein, we present the mechanochemical synthesis of three new cocrystals containing the API carbamazepine (cocrystals CBZ:Indometacin 1:1, CBZ:Benzamide 1:1, and CBZ:Nifedipine 1:1). The mechanochemical reaction was investigated in situ documenting a fast and complete reaction within one minute. Online NMR spectroscopy proved the direct influence of the dissolution behaviour of the coformers to the dissolution behaviour of the API carbamazepine. The dissolution behaviour of the organic cocrystals is compared to the behaviour of the pure drug indicating a general applicability of this approach for detailed cocrystal dissolution studies.

  6. Facile Synthesis of Au Nanocube-CdS Core-Shell Nanocomposites with Enhanced Photocatalytic Activity

    Science.gov (United States)

    Liu, Xiao-Li; Liang, Shan; Li, Min; Yu, Xue-Feng; Zhou, Li; Wang, Qu-Qua

    2014-06-01

    Au nanocube-CdS core-shell nanocomposites are prepared by using a one-pot method in aqueous phase with cetyltrimethylammonium bromide as the surfactant. The extinction properties and photocatalytic activity of Au-CdS nanocomposites are investigated. Compared with the pure Au nanocubes, the Au-CdS nanocomposites exhibit enhanced extinction intensity. Compared with CdS nanoparticles, the Au-CdS nanocomposites exhibit improved photocatalytic activity. Furthermore, the photocatalytic efficiency is even better with the increase in the core size of the Au-CdS nanocomposites. Typically, the photocatalytic efficiency of the Au-CdS with 62 nm sized Au nanocubes is about two times higher than that of the pure CdS. It is believed that the Au-CdS nanocomposites may find potential applications in environmental fields, and this synthesis method can be extended to prepare a wide variety of functional composites with Au cores.

  7. One step synthesis of porous graphene by laser ablation: A new and facile approach

    Science.gov (United States)

    Kazemizadeh, Fatemeh; Malekfar, Rasoul

    2018-02-01

    Porous graphene (PG) was obtained using one step laser process. Synthesis was carried out by laser ablation of nickel-graphite target under ultra-high flow of argon gas. The field emission scanning electron microscopy (FE-SEM) results showed the formation of a porous structure and the transmission electron microscopy (TEM) revealed that the porosity of PGs increase under intense laser irradiation. Structural characterization study using Raman spectroscopy, X-ray powder diffraction (XRD) and selected area electron diffraction (SAED) technique showed that the obtained PGs display high crystalline structure in the form of few layer rhombohedral graphitic arrangement that can be interpreted as the phase prior to the formation of other carbon nanostructures.

  8. Silica-gel Catalyzed Facile Synthesis of 3,4-Dihydropyrimidinones

    International Nuclear Information System (INIS)

    Agarwal, Sameer; Aware, Umesh; Patil, Amit; Rohera, Vinita; Jain, Mukul; Patel, Pankaj; Ghate, Manjunath

    2012-01-01

    We have developed a mild and highly effective procedure for the one-pot synthesis of substituted dihydropyrimidinones in high yields using silica gel as a green, highly efficient and recyclable heterogeneous catalyst. Our approach can be applied to the preparation of a wide range of synthetic analogues for structure-activity studies. Investigations in this direction are ongoing. The pyrimidinone ring is a basic substructure of numerous biologically active alkaloids and pharmaceutical products. These cores are regarded as one of the most important groups of drug-like scaffolds. 3,4-dihydropyrimidinones above are known to exhibit variety of pharmacological activity such as calcium channel modulation, mitotic kinesin Eg5 inhibition, antiviral, anti-inflammatory, antibacterial activity, etc

  9. Silica-gel Catalyzed Facile Synthesis of 3,4-Dihydropyrimidinones

    Energy Technology Data Exchange (ETDEWEB)

    Agarwal, Sameer; Aware, Umesh; Patil, Amit; Rohera, Vinita; Jain, Mukul; Patel, Pankaj [Zydus Research Centre, Sarkhej-Bavla N.H., Ahmedabad (India); Ghate, Manjunath [Nirma University, Ahmedabad (India)

    2012-02-15

    We have developed a mild and highly effective procedure for the one-pot synthesis of substituted dihydropyrimidinones in high yields using silica gel as a green, highly efficient and recyclable heterogeneous catalyst. Our approach can be applied to the preparation of a wide range of synthetic analogues for structure-activity studies. Investigations in this direction are ongoing. The pyrimidinone ring is a basic substructure of numerous biologically active alkaloids and pharmaceutical products. These cores are regarded as one of the most important groups of drug-like scaffolds. 3,4-dihydropyrimidinones above are known to exhibit variety of pharmacological activity such as calcium channel modulation, mitotic kinesin Eg5 inhibition, antiviral, anti-inflammatory, antibacterial activity, etc.

  10. Facile synthesis and herbicidal evaluation of 2-aryl-4h-3, 1-benzoxazin-4-ones

    International Nuclear Information System (INIS)

    Hussain, Z.; Khan, Z.A.

    2013-01-01

    The present work deals with the synthesis of 4H-3,1-benzoxazin-4-ones carrying an aryl functional group at position-2. Synthesized compounds tested for herbicidal activity at three different doses (500 micro g/mL, 50 micro g/mL and 5 micro g/mL). Most of the compounds exhibited significant herbicidal activity against Lemna aequinocitalis welv at higher dose (500 micro g/mL). Among the tested compounds 2-phenyl-4H-3,1-benzoxazin-4-one (3a) and 2-(3-chlorophenyl)-4H-3,1-benzoxazin-4-one (3l) completely inhibited the plant growth at 500 and 50 micro g/mL concentrations. All the synthetic compounds were characterized by FT-IR, 1H NMR, EI-MS and elemental analysis. (author)

  11. Facile Synthesis of Silver Nanocubes with Sharp Corners and Edges in an Aqueous Solution.

    Science.gov (United States)

    Zhou, Shan; Li, Jianhua; Gilroy, Kyle D; Tao, Jing; Zhu, Chunlei; Yang, Xuan; Sun, Xiaojun; Xia, Younan

    2016-11-22

    It remains a challenge to synthesize Ag nanocubes in an aqueous system, although the polyol process was successfully adopted more than one decade ago. Here, we report an aqueous method for the synthesis of Ag nanocubes with an average edge length of 35-95 nm. It involves the formation of AgCl octahedra by mixing CF 3 COOAg with cetyltrimethylammonium chloride, followed by the nucleation and growth of Ag nanocrystals in the presence of ascorbic acid (AA) and FeCl 3 . The Fe 3+ /Fe 2+ redox pair is responsible for the removal of multiply twinned seeds through oxidative etching. The Cl - ions play two critical roles in the nucleation and growth of Ag nanocubes with a single-crystal structure. First, the Cl - ions react with Ag + ions to generate nanometer-sized AgCl octahedra in the initial stage of a synthesis. In the presence of room light and a proper reducing agent such as AA, the AgCl can be reduced to generate Ag n nuclei followed by their evolution into single-crystal seeds and then Ag nanocrystals. Second, the Cl - ions can act as a specific capping agent toward the Ag(100) surface, enabling the formation of Ag nanocubes with sharp corners and edges. Based on the results from a set of time-lapse studies and control experiments, we formulate a plausible mechanism to account for the formation of Ag nanocubes that resembles the formation and development of latent image centers in silver halide grains in the photographic process.

  12. Synthesis of sulfonated porous carbon nanospheres solid acid by a facile chemical activation route

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Binbin, E-mail: changbinbin806@163.com; Guo, Yanzhen; Yin, Hang; Zhang, Shouren; Yang, Baocheng, E-mail: baochengyang@yahoo.com

    2015-01-15

    Generally, porous carbon nanospheres materials are usually prepared via a template method, which is a multi-steps and high-cost strategy. Here, we reported a porous carbon nanosphere solid acid with high surface area and superior porosity, as well as uniform nanospheical morphology, which prepared by a facile chemical activation with ZnCl{sub 2} using resorcinol-formaldehyde (RF) resins spheres as precursor. The activation of RF resins spheres by ZnCl{sub 2} at 400 °C brought high surface area and large volume, and simultaneously retained numerous oxygen-containing and hydrogen-containing groups due to the relatively low processing temperature. The presence of these functional groups is favorable for the modification of –SO{sub 3}H groups by a followed sulfonation treating with sulphuric acid and organic sulfonic acid. The results of N{sub 2} adsorption–desorption and electron microscopy clearly showed the preservation of porous structure and nanospherical morphology. Infrared spectra certified the variation of surface functional groups after activation and the successful modification of –SO{sub 3}H groups after sulfonation. The acidities of catalysts were estimated by an indirect titration method and the modified amount of –SO{sub 3}H groups were examined by energy dispersive spectra. The results suggested sulfonated porous carbon nanospheres catalysts possessed high acidities and –SO{sub 3}H densities, which endowed their significantly catalytic activities for biodiesel production. Furthermore, their excellent stability and recycling property were also demonstrated by five consecutive cycles. - Graphical abstract: Sulfonated porous carbon nanospheres with high surface area and superior catalytic performance were prepared by a facile chemical activation route. - Highlights: • Porous carbon spheres solid acid prepared by a facile chemical activation. • It owns high surface area, superior porosity and uniform spherical morphology. • It possesses

  13. A facile approach towards synthesis, characterization, single crystal structure, and DFT study of 5-bromosalicylalcohol

    Energy Technology Data Exchange (ETDEWEB)

    Rastogi, Rupali, E-mail: rastogirupali@ymail.com [ITM University, Department of Chemistry (India); Tarannum, Nazia [Ch. Charan Singh University, Department of Chemistry (India); Butcher, R. J. [Howard University, Chemistry Department (United States)

    2016-03-15

    5-Bromosalicylalcohol was prepared by the interaction of NaBH{sub 4} and 5-bromosalicylaldehyde. The use of sodium borohydride makes the reaction easy, facile, economic and does not require any toxic catalyst. The compound is characterized by FTIR, {sup 1}H NMR, {sup 13}C NMR, TEM and ESI-mass spectra. Crystal structure is determined by single crystal X-ray analysis. Quantum mechanical calculations of geometries, energies and thermodynamic parameters are carried out using density functional theory (DFT/B3LYP) method with 6-311G(d,p) basis set. The optimized geometrical parameters obtained by B3LYP method show good agreement with experimental data.

  14. Facile synthesis of polypyrrole nanowires for high-performance supercapacitor electrode materials

    OpenAIRE

    Zhao, Junhong; Wu, Jinping; Li, Bing; Du, Weimin; Huang, Qingli; Zheng, Mingbo; Xue, Huaiguo; Pang, Huan

    2016-01-01

    Polypyrrole nanowires are facile synthesized under a mild condition with FeCl3 as an oxidant. Polypyrrole nanowires with the width of 120 nm form many nanogaps or pores due to the intertwined nanostructures. More importantly, PPy nanowires were further applied for supercapacitor electrode materials. After electrochemical testing, it was observed that the PPy nanowire based electrode showed a large specific capacitance (420 F g−1, 1.5 A g−1) and good rate capability (272 F g−1, 18.0 A g−1), wh...

  15. Facile Synthesis of Long, Straight and Uniform Copper Nanowires via a Solvothermal Method

    Institute of Scientific and Technical Information of China (English)

    Chunfu Lin; Hong Lin; Ning Wang; Xing Zhang; Jun Yang; Jianbo Li; Xiaozhan Yang

    2006-01-01

    Copper nanowires were facilely prepared via a solvothermal method. In this method, cetyltrimethylammonium bromide (CTAB) was used as a soft template, copper nitrate was an inorganic precursor, and absolute ethanol served as a reducing agent as well as a solvent. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to characterize the as-prepared copper nanowires. The as-prepared copper nanowires are fairly uniform and long. The majority of them are longer than 100 μm and some even longer than 200 μm. Furthermore, most nanowires are quite straight. In addition,The mechanism of the growth process of copper nanowires was discussed.

  16. Facile Synthesis of Magnetic Mesoporous Hollow Carbon Microspheres for Rapid Capture of Low-Concentration Peptides

    OpenAIRE

    Cheng, Gong; Zhou, Ming-Da; Zheng, Si-Yang

    2014-01-01

    Mesoporous and hollow carbon microspheres embedded with magnetic nanoparticles (denoted as MHM) were prepared via a facile self-sacrificial method for rapid capture of low-abundant peptides from complex biological samples. The morphology, structure, surface property, and magnetism were well-characterized. The hollow magnetic carbon microspheres have a saturation magnetization value of 130.2 emu g?1 at room temperature and a Brunauer?Emmett?Teller specific surface area of 48.8 m2 g?1 with an a...

  17. Facile Synthesis of Nitrogen-doped Carbon Quantum Dots for Bio-imaging

    Directory of Open Access Journals (Sweden)

    de Yro Persia Ada N.

    2016-01-01

    Full Text Available Carbon quantum dots (CQD with fascinating properties has gradually become a rising star as a new nanocarbon member due to its nonthreatening, abundant and inexpensive nature. This study reports on a facile preparation of fluorescent carbon quantum dots (CQD from iota Carrageenan. CQD from iota Carrageenan was produced by hydrothermal method with a quantum yield (QY of 16 to 20%. Doping the CQD with nitrogen by the addition of tetraethylene pentamine (TEPE produced CQD with a QY of 77%. FTIR data confirmed the formation of hydroxyl, carboxylic and carbonyl functional groups as confirmed by the ToFSIMS data due to the presence of nitrogen bonds on the N-CQD produced with TEPE. The CQD and N-CQD produced are crystalline with graphitic structures because of the presence of sp2 graphitic d line spacing with the sizes ranging from 2 to 10nm. To examine the feasibility of using the CQD as nanoprobe in practical applications, labelling and detection of E.coli was performed. The E.coli fluoresced proving CQD as an effective probe in bio imaging application. This study has successfully demonstrated a facile approach of producing CQD with significant high quantum yields to fluorescent CQD for bio imaging applications.

  18. Tricobalt tetroxide nanoplate arrays on flexible conductive fabric substrate: Facile synthesis and application for electrochemical supercapacitors

    Science.gov (United States)

    Nagaraju, Goli; Ko, Yeong Hwan; Yu, Jae Su

    2015-06-01

    Tricobalt tetroxide (Co3O4) nanoplate arrays (NPAs) were synthesized on flexible conductive fabric substrate (FCFs) by a facile two-electrode system based electrochemical deposition method, followed by a simple heat treatment process. Initially, cobalt hydroxide (Co(OH)2) NPAs were electrochemically deposited on FCFs by applying an external voltage of -1.5 V for 30 min. Then, the Co3O4 NPAs on FCFs was obtained by thermal treatment of as-deposited Co(OH)2 NPAs on FCFs at 200 °C for 2 h. From the analysis of morphological and crystal properties, the Co3O4 NPAs were well integrated and uniformly covered over the entire surface of substrate with good crystallinity in the cubic phase. Additionally, the fabricated sample was directly used as a binder-free electrode to examine the feasibility for electrochemical supercapacitors using cyclic voltammetry and galvanic charge-discharge measurements in 1 M KOH electrolyte solution. The Co3O4 NPAs coated FCFs electrode exhibited a maximum specific capacitance of 145.6 F/g at a current density of 1 A/g and an excellent rate capability after 1000 cycles at a current density of 3 A/g. This facile fabrication method for integrating the Co3O4 nanostructures on FCFs could be a promising approach for advanced flexible electronic and energy-storage device applications.

  19. Hexagonal pencil-like CdS nanorods: Facile synthesis and enhanced visible light photocatalytic performance

    Science.gov (United States)

    An, Liang; Wang, Guanghui; Zhao, Lei; Zhou, Yong; Gao, Fang; Cheng, Yang

    2015-07-01

    In the present study, hexagonal pencil-like CdS nanorods have been successfully synthesized through a typical facile and economical one-step hydrothermal method without using any surfactant or template. The product was characterized by X-ray powder diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and energy dispersive analysis of X-ray (EDX). The results revealed that the prepared CdS photocatalyst consisted of a large quantity of straight and smooth solid hexagonal nanorods and a few nanoparticles. The photocatalytic activities of CdS nanorods and commercial CdS powders were investigated by the photodegradation of Orange II (OII) in aqueous solution under visible light, and the CdS nanorods presented the highest photocatalytic activity. Its photocatalytic efficiency enhancement was attributed to the improved transmission of photogenerated electron-hole pairs in the CdS nanostructures. The present findings may provide a facile approach to synthesize high efficient CdS photocatalysts.

  20. A facile homogeneous precipitation synthesis of NiO nanosheets and their applications in water treatment

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Junfeng, E-mail: daidai02304@163.com [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Jiangsu Laboratory of Advanced Functional Materials, Changshu Institute of Technology, Changshu (China); Tan, Yang; Su, Kang; Zhao, Junjie; Yang, Chen; Sang, Lingling [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Lu, Hongbin [National Laboratory of Solid State Microstructures and College of Engineering and Applied Sciences, Nanjing University, Nanjing (China); Chen, JianHua [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu (China); Jiangsu Laboratory of Advanced Functional Materials, Changshu Institute of Technology, Changshu (China)

    2015-05-15

    Highlights: • NiO nanosheets were synthesized via a facile homogeneous precipitation method. • The NiO nanosheets have a large surface area. • This preparation method was low-cost, simple equipments, easy preparation, short reaction time and better repeatability. • The product also showed a favourable ability to remove Cr(VI) and Congo red (CR) in water treatment. - Abstract: NiO nanosheets were successfully synthesized by a facile homogeneous precipitation method with the assistance of ethanol amine. The sample was characterized by X-ray diffraction (XRD), scanning electronic microscopy (SEM), transmission electron microscopy (TEM), and nitrogen adsorption–desorption techniques. The results demonstrated that the as-prepared product was cubic NiO nanosheets with a large surface area of 170.1 m{sup 2} g{sup −1}. Further, the as-prepared product was used to investigate its potential application for wastewater treatment. The maximum adsorption capacity for Cr(VI) and Congo red (CR) on NiO nanosheets has been determined using the Langmuir equation and found to reach up to 48.98 and 167.73 mg g{sup −1}, respectively. It could be concluded that NiO nanosheets with special surface features had the potential as adsorbents for wastewater treatment.

  1. Facile synthesis of birnessite-type manganese oxide nanoparticles as supercapacitor electrode materials.

    Science.gov (United States)

    Liu, Lihu; Luo, Yao; Tan, Wenfeng; Zhang, Yashan; Liu, Fan; Qiu, Guohong

    2016-11-15

    Manganese oxides are environmentally benign supercapacitor electrode materials and, in particular, birnessite-type structure shows very promising electrochemical performance. In this work, nanostructured birnessite was facilely prepared by adding dropwise NH2OH·HCl to KMnO4 solution under ambient temperature and pressure. In order to fully exploit the potential of birnessite-type manganese oxide electrode materials, the effects of specific surface area, pore size, content of K(+), and manganese average oxidation state (Mn AOS) on their electrochemical performance were studied. The results showed that with the increase of NH2OH·HCl, the Mn AOS decreased and the corresponding pore sizes and specific surface area of birnessite increased. The synthesized nanostructured birnessite showed the highest specific capacitance of 245Fg(-1) at a current density of 0.1Ag(-1) within a potential range of 0-0.9V, and excellent cycle stability with a capacitance retention rate of 92% after 3000 cycles at a current density of 1.0Ag(-1). The present work implies that specific capacitance is mainly affected by specific surface area and pore volume, and provides a new method for the facile preparation of birnessite-type manganese oxide with excellent capacitive performance. Copyright © 2016 Elsevier Inc. All rights reserved.

  2. Facile synthesis of MnO{sub 2}/CNT nanocomposite and its electrochemical performance for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Wang Hongjuan, E-mail: cehjwang@scut.edu.cn [School of Chemistry and Chemcial Engineering, South China University of Technology, Guangzhou, 510640 (China); Peng Cheng [School of Chemistry and Chemcial Engineering, South China University of Technology, Guangzhou, 510640 (China); Peng Feng, E-mail: cefpeng@scut.edu.cn [School of Chemistry and Chemcial Engineering, South China University of Technology, Guangzhou, 510640 (China); Yu Hao; Yang Jian [School of Chemistry and Chemcial Engineering, South China University of Technology, Guangzhou, 510640 (China)

    2011-08-25

    Highlights: > MnO{sub 2}/CNTs are prepared by direct redox reaction between KMnO{sub 4} and carbon nanotubes. > This preparation method is a simple and green without any other additives. > MnO{sub 2}/CNTs show specific capacitance of 162.2 F g{sup -1} at the current density of 0.2 A g{sup -1}. > MnO{sub 2}/CNTs exhibit excellent charge-discharge property. - Abstract: A nanocomposite of manganese dioxide coated on the carbon nanotubes (MnO{sub 2}/CNTs) was synthesized by a facile direct redox reaction between potassium permanganate and carbon nanotubes without any other oxidant or reductant addition. The morphology, microstructure and crystalline form of this MnO{sub 2}/CNT nanocomposite were characterized by scanning electron microscopy (SEM), transition electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The electrochemical properties are characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge/discharge (GCD). The results show that the facile prepared MnO{sub 2}/CNTs nanocomposite shows specific capacitance of 162.2 F g{sup -1} at the current density of 0.2 A g{sup -1} and excellent charge/discharge property with 90% of its specific capacitance kept after 2000 cycles at the current density of 5 A g{sup -1}.

  3. Diatomite-immobilized BiOI hybrid photocatalyst: Facile deposition synthesis and enhanced photocatalytic activity

    Science.gov (United States)

    Li, Baoying; Huang, Hongwei; Guo, Yuxi; Zhang, Yihe

    2015-10-01

    A novel diatomite-immobilized BiOI hybrid photocatalyst has been prepared by a facile one-step deposition process for the first time. The structure, morphology and optical property of the products were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and UV-vis diffuse reflectance spectroscopy (DRS). The photocatalytic performance of the as-prepared BiOI/diatomite photocatalysts was studied by photodegradation of Rhodamine B (RhB) and methylene blue (MB) and monitoring photocurrent generation under visible light (λ > 420 nm). The results revealed that BiOI/diatomite composites exhibit enhanced photocatalytic activity compared to the pristine BiOI sample. This enhancement should be attributed to that diatomite can play as an excellent carrier platform to increase the reactive sites and promote the separation of photogenerated electron-hole pairs. In addition, the corresponding photocatalytic mechanism was proposed based on the active species trapping experiments. This work shed new light on facile fabrication of novel composite photocatalyst based on natural mineral.

  4. Facile and large-scale synthesis and characterization of carbon nanotube/silver nanocrystal nanohybrids

    International Nuclear Information System (INIS)

    Gao Chao; Li Wenwen; Jin Yizheng; Kong Hao

    2006-01-01

    A facile and efficient aqueous phase-based strategy to synthesize carbon nanotube (CNT)/silver nanocrystal nanohybrids at room temperature is reported. In the presence of carboxyl group functionalized or poly(acrylic acid)- (PAA-) grafted CNTs, silver nanoparticles were in situ generated from AgNO 3 aqueous solution, without any additional reducing agent or irradiation treatment, and readily attached to the CNT convex surfaces, leading to the CNT/Ag nanohybrids. The produced silver nanoparticles were determined to be face-centred cubic silver nanocrystals by scanning transmission electron microscopy (STEM), electron diffraction (ED) and x-ray powder diffraction (XRD) analyses. Detailed experiments showed that this strategy can also be applied to different CNTs, including single-walled carbon nanotubes (SWNTs), double-walled carbon nanotubes (DWNTs), multiwalled carbon nanotubes (MWNTs), and polymer-functionalized CNTs. The nanoparticle sizes can be controlled from 2 nm to 10-20 nm and the amount of metal deposited on CNT surfaces can be as high as 82 wt%. Furthermore, large-scale (10 g or more) CNT/Ag nanohybrids can be prepared via this approach without the decrease of efficiency and quality. This approach can also be extended to prepare Au single crystals by CNTs. The facile, efficient and large-scale availability of the nanohybrids makes their tremendous potential realizable and developable

  5. Combustion strategy : United Kingdom

    Energy Technology Data Exchange (ETDEWEB)

    Greenhalgh, D. [Heriot-Watt Univ., Edingburgh, Scotland (United Kingdom). School of Engineering and Physical Sciences

    2009-07-01

    The United Kingdom's combustion strategy was briefly presented. Government funding sources for universities were listed. The United Kingdom Research Councils that were listed included the Arts and Humanities Research Council (AHRC) and the Biotechnology and Biological Sciences Research Council (BBSRC); the Engineering and Physical Sciences Research Council (EPSRC); the Economic and Social Research Council; the Medical Research Council; the Natural Environment Research Council; and the Science and Technology Facilities Council. The EPSRC supported 65 grants worth 30.5 million pounds. The combustion industry was noted to be dominated by three main players of which one was by far the largest. The 3 key players were Rolls-Royce; Jaguar Land Rover; and Doosan Babcock. Industry and government involvement was also discussed for the BIS Technology Strategy Board, strategy technology areas, and strategy application areas.

  6. A facile synthesis of nanorods of ZnO/graphene oxide composites with enhanced photocatalytic activity

    International Nuclear Information System (INIS)

    Qin, Jiaqian; Zhang, Xinyu; Xue, Yannan; Kittiwattanothai, Nutsakun; Kongsittikul, Pongsakorn; Rodthongkum, Nadnudda; Limpanart, Sarintorn; Ma, Mingzhen; Liu, Riping

    2014-01-01

    Graphical abstract: - Highlights: • Room temperature method to prepare ZnO–GO composites. • ZnO–GO composites exhibit superior absorption ability and photocatalytic performance. • With GO content increasing, the absorption and photocatalytic ability increased. - Abstract: Graphene oxide (GO)–ZnO nanorods composites were successfully synthesized by a facile room-temperature approach using the colloidal coagulation effect. The samples are characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, specific surface area, and UV–vis spectroscopy. The photodegradation of methylene blue (MB) has been investigated in the presence of composites. It is observed that the absorption capacity and photocatalytic effect could be enhanced by adding graphene oxide

  7. A Facile, Choline Chloride/Urea Catalyzed Solid Phase Synthesis of Coumarins via Knoevenagel Condensation

    Directory of Open Access Journals (Sweden)

    Hosanagara N. Harishkumar

    2011-01-01

    Full Text Available The influence of choline chloride/urea ionic liquid in solid phase on the Knoevenagel condensation is demonstrated. The active methylene compounds such as meldrum’s acid, diethylmalonate, ethyl cyanoacetate, dimethylmalonate, were efficiently condensed with various salicylaldehydes in presence of choline chloride/urea ionic liquid without using any solvents or additional catalyst. The reaction is remarkably facile because of the air and water stability of the catalyst, and needs no special precautions. The reactions were completed within 1hr with excellent yields (95%. The products formed were sufficiently pure, and can be easily recovered. The use of ionic liquid choline chloride/urea in solid phase offered several significant advantages such as low cost, greater selectivity and easy isolation of products.

  8. Facile Synthesis of Polyaniline Nanotubes with Square Capillary Using Urea as Template

    Directory of Open Access Journals (Sweden)

    Shuhua Pang

    2017-10-01

    Full Text Available Polyaniline nanotubes were successfully synthesized by a facile in situ chemical oxidative polymerization method using urea as soft template. When the urea/aniline molar ratio is 3:1, the as-prepared nanotubular polyaniline (PANI-3 shows regular and uniform square capillaries, which provides a high electrode/electrolyte contact, easy ion diffusion and enhanced electroactive regions during the electrochemical process, leading to weak internal resistance and improved electrochemical performance. The PANI-3 sample exhibits a high specific capacitance of 405 F/g at current density of 0.2 A/g, and PANI only has a specific capacitance of 263 F/g. At current density of 1 A/g, the capacitance of PANI-3 is still 263 F/g (64.9% of the capacitance at 0.2 A/g. Such a PANI-3 nanotube, with regular and uniform capillary, is a promising electrode material for high-performance supercapacitors.

  9. Facile synthesis of graphene on single mode fiber via chemical vapor deposition

    International Nuclear Information System (INIS)

    Zhang, C.; Man, B.Y.; Jiang, S.Z.; Yang, C.; Liu, M.; Chen, C.S.; Xu, S.C.; Feng, D.J.; Bi, D.; Liu, F.Y.; Qiu, H.W.

    2014-01-01

    Direct deposition of graphene film on the standard single mode fiber is offered using a Cu-vapor-assisted chemical vapor deposition system. The gas flow of H 2 and Ar before the growth process plays a crucial role for the direct deposition of the graphene film and the layers of the graphene can be controlled by the growth time. With a large gas flow, Cu atoms are carried off with the gas flow and hard to deposit on the surface of the single mode fiber before the growth process. Consequently, uniform graphene film is obtained in this case. On the contrary, with a lower one, Cu atoms is facile to deposit on the surface of the single mode fiber and form nanodots acting as active catalytic sites for the growth of carbon nanotubes. This method presents us a promising transfer-free technique for fabrication of the photonic applications.

  10. Facile synthesis of highly aligned multiwalled carbon nanotubes from polymer precursors.

    Energy Technology Data Exchange (ETDEWEB)

    Han, C. Y.; Xiao, Z.-L.; Wang, H. H.; Lin, X.-M.; Trasobares, S.; Cook, R. E.; Richard J. Daley Coll.; Northern Illinois Univ.; Univ. de Cadiz

    2009-01-01

    We report a facile one-step approach which involves no flammable gas, no catalyst, and no in situ polymerization for the preparation of well-aligned carbon nanotube array. A polymer precursor is placed on top of an anodized aluminum oxide (AAO) membrane containing regular nanopore arrays, and slow heating under Ar flow allows the molten polymer to wet the template through adhesive force. The polymer spread into the nanopores of the template to form polymer nanotubes. Upon carbonization the resulting multi-walled carbon nanotubes duplicate the nanopores morphology precisely. The process is demonstrated for 230, 50, and 20 nm pore membranes. The synthesized carbon nanotubes are characterized with scanning/transmission electron microscopies, Raman spectroscopy, and resistive measurements. Convenient functionalization of the nanotubes with this method is demonstrated through premixing CoPt nanoparticles in the polymer precursors.

  11. Ultrafine ferromagnetic iron oxide nanoparticles: Facile synthesis by low temperature decomposition of iron glycerolate

    Energy Technology Data Exchange (ETDEWEB)

    Bartůněk, Vilém, E-mail: vilem.bartunek@vscht.cz [Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic); Průcha, David [Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic); Švecová, Marie [Department of Analytical Chemistry, Faculty of Chemical Engineering, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic); Ulbrich, Pavel [Department of Biochemistry and Microbiology, Faculty of Food and Biochemical Technology, University of Chemistry and Technology, Technická 3, 166 28 Prague 6 (Czech Republic); Huber, Štěpán; Sedmidubský, David; Jankovský, Ondřej [Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology, Technická 5, 166 28 Prague 6 (Czech Republic)

    2016-09-01

    We synthesized dark colored ultrafine – sub 10 nm iron oxide nanoparticles by a facile and low temperature process based on thermal decomposition of an affordable precursor – iron glycerolate. Simultaneous thermal analysis (STA) was used to study the thermal behaviour during the decomposition. The iron glycerolate was thoroughly analysed by various methods. The size of the iron nanoparticles was determined from XRD patterns and by transmission electron microscopy (TEM) and their composition has been confirmed by XPS. Magnetic properties of the nanoparticles were studied by vibrating sample magnetometry. The prepared single phase material exhibiting ferromagnetic properties is usable in a wide range of applications and may be suitable even for large scale industrial applications. - Highlights: • Iron glycerolate prepared and characterised. • Iron oxide nanoparticles prepared by thermal decomposition of iron glycerolate. • STA used to study the decomposition. • Products characterised by XRD, XPS, FT-IR, SEM and TEM. • Magnetic behaviour of monophasic samples determined.

  12. Facile synthesis of polypyrrole nanowires for high-performance supercapacitor electrode materials

    Directory of Open Access Journals (Sweden)

    Junhong Zhao

    2016-06-01

    Full Text Available Polypyrrole nanowires are facile synthesized under a mild condition with FeCl3 as an oxidant. Polypyrrole nanowires with the width of 120 nm form many nanogaps or pores due to the intertwined nanostructures. More importantly, PPy nanowires were further applied for supercapacitor electrode materials. After electrochemical testing, it was observed that the PPy nanowire based electrode showed a large specific capacitance (420 F g−1, 1.5 A g−1 and good rate capability (272 F g−1, 18.0 A g−1, which is larger than that of most of published results. The as-prepared electrode can work well even after 8000 cycles at 1.5 A g−1.

  13. Design of generic coal conversion facilities: Indirect coal liquefaction, Fischer-Tropsch synthesis

    Energy Technology Data Exchange (ETDEWEB)

    1991-10-01

    A comprehensive review of Fischer-Tropsch (F-T) technology, including fixed, fluidized, and bubble column reactors, was undertaken in order to develop an information base before initiating the design of the Fischer-Tropsch indirect liquefaction PDU as a part of the Generic Coal Conversion Facilities to be built at the Pittsburgh Energy Technology Center (PETC). The pilot plant will include a fixed bed and slurry bubble column reactor for the F-T mode of operation. The review encompasses current status of both these technologies, their key variables, catalyst development, future directions, and potential improvement areas. However, more emphasis has been placed on the slurry bubble column reactor since this route is likely to be the preferred technology for commercialization, offering process advantages and, therefore, better economics than fixed and fluidized bed approaches.

  14. Facile Synthesis of Highly Aligned Multiwalled Carbon Nanotubes from Polymer Precursors

    Directory of Open Access Journals (Sweden)

    Catherine Y. Han

    2009-01-01

    Full Text Available We report a facile one-step approach which involves no flammable gas, no catalyst, and no in situ polymerization for the preparation of well-aligned carbon nanotube array. A polymer precursor is placed on top of an anodized aluminum oxide (AAO membrane containing regular nanopore arrays, and slow heating under Ar flow allows the molten polymer to wet the template through adhesive force. The polymer spread into the nanopores of the template to form polymer nanotubes. Upon carbonization the resulting multi-walled carbon nanotubes duplicate the nanopores morphology precisely. The process is demonstrated for 230, 50, and 20 nm pore membranes. The synthesized carbon nanotubes are characterized with scanning/transmission electron microscopies, Raman spectroscopy, and resistive measurements. Convenient functionalization of the nanotubes with this method is demonstrated through premixing CoPt nanoparticles in the polymer precursors.

  15. Facile synthesis of polymer-enveloped ultrasmall superparamagnetic iron oxide for magnetic resonance imaging

    International Nuclear Information System (INIS)

    Hong Jun; Xu Dongmei; Yu Jiahui; Gong Peijun; Ma Hongjuan; Yao Side

    2007-01-01

    Ultrasmall superparamagnetic iron oxide (USPIO) with synthetic polymer, based on magnetite core, was synthesized via facile photochemical in situ polymerization. A possible mechanism of photochemical in situ polymerization was proposed. The obtained polymer-enveloped UPSIO was characterized by transmission electron microscopy (TEM), photo-correlation spectroscopy (PCS), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric (TG) analysis and vibrating sampling magnetometer (VSM) measurement. Properties such as ultrasmall particle size, hydrophilicity, strong magnetization and surface characteristics, which are desirable for magnetic resonance imaging (MRI) contrast agents, were evaluated in detail. The resultant USPIO-based MRI contrast agent holds considerable promise in molecular MR tracking, MR immune imaging, cell tracking and targeted intracellular hyperthermia, etc

  16. Microwave-induced facile synthesis of water-soluble fluorogenic alginic acid derivatives.

    Science.gov (United States)

    Chhatbar, Mahesh U; Meena, Ramavatar; Prasad, Kamalesh; Chejara, Dharmesh R; Siddhanta, A K

    2011-04-01

    A facile microwave-induced method was developed for synthesizing water-soluble fluorescent derivatives of alginic acid (ALG) with four different diamines, hydrazine (HY), ethylenediamine (EDA), 1,6-hexanediamine (HDA), and 1,4-cyclohexanediamine (CHDA), followed by a cross-linking reaction with a natural cross linker genipin. The ethylenediamine derivative of alginic acid (ALG-EDA) exhibited good fluorescent activity, which upon cross linking was enhanced threefold. The other amide derivatives, for example, ALG-HY, ALG-HDA, and ALG-CHDA, were not fluorescent, but their respective crosslinked products exhibited excellent fluorescent activity. The fluorescence intensity had an inverse correlation with the number of carbon atoms present in the amine, which in turn was a function of degree of substitution (DS). These fluorescent polysaccharide derivatives are of potential utility in the domain of sensor applications. Copyright © 2011 Elsevier Ltd. All rights reserved.

  17. Facile Synthesis of Porous Silicon Nanofibers by Magnesium Reduction for Application in Lithium Ion Batteries.

    Science.gov (United States)

    Cho, Daehwan; Kim, Moonkyoung; Hwang, Jeonghyun; Park, Jay Hoon; Joo, Yong Lak; Jeong, Youngjin

    2015-12-01

    We report a facile fabrication of porous silicon nanofibers by a simple three-stage procedure. Polymer/silicon precursor composite nanofibers are first fabricated by electrospinning, a water-based spinning dope, which undergoes subsequent heat treatment and then reduction using magnesium to be converted into porous silicon nanofibers. The porous silicon nanofibers are coated with a graphene by using a plasma-enhanced chemical vapor deposition for use as an anode material of lithium ion batteries. The porous silicon nanofibers can be mass-produced by a simple and solvent-free method, which uses an environmental-friendly polymer solution. The graphene-coated silicon nanofibers show an improved cycling performance of a capacity retention than the pure silicon nanofibers due to the suppression of the volume change and the increase of electric conductivity by the graphene.

  18. Facile synthesis of deoxycholate intercalated layered double hydroxide nanohybrids via a coassembly process

    International Nuclear Information System (INIS)

    Wu, Xiaowen; Wang, Shuang; Du, Na; Zhang, Renjie; Hou, Wanguo

    2013-01-01

    In this paper, we describe a synthesis strategy of deoxycholate (DC) intercalated layered double hydroxide (LDH) nanohybrids via a coassembly method at room temperature. For this strategy, LDH particles were delaminated to well-dispersed 2D nanosheets in formamide, and the resulting LDH nanosheets were then coassembled with DC anions into the DC intercalated LDH (DC-LDH) nanohybrids. The so-synthesized nanohybrids were characterized by XRD, TEM, FT-IR, elemental analyses and TG-DSC. It was found that the loading amount of DC in the nanohybrids could be easily controlled by changing the ratio of DC to LDH. In addition, the nanohybrids have similar characteristics with the DC-LDH nanohybrids synthesized by the hydrothermal method, including their DC loading, crystal structure, morphology and thermal gravimetric behavior. However, this strategy exhibited the advantages of short reaction time and mild experimental conditions compared with the hydrothermal method. - Graphical abstract: Deoxycholate intercalated layered double hydroxide nanohybrids were successfully synthesized via a coassembly strategy. In this strategy, the interlayer spaces of LDHs can be efficiently used for the intercalation of guest species. - Highlights: • Deoxycholate intercalated layered double hydroxide nanohybrids were synthesized via a coassembly strategy. • This strategy exhibited the advantages of short time and mild conditions. • This strategy can enable organic species to be readily intercalated into the LDH galleries

  19. Facile synthesis of mesostructured ZSM-5 zeolite with enhanced mass transport and catalytic performances

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chao; Ren, Yanqun [School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Tianhe District, Guangzhou 510641 (China); Gou, Jinsheng [College Material Science and Technology, Beijing Forestry University, Key Laboratory of Wooden Material Science and Application, Ministry of Education, 35 Tsinghua East Road, Haidian District, Beijing 100083 (China); Liu, Baoyu [School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Tianhe District, Guangzhou 510641 (China); Xi, Hongxia, E-mail: cehxxi@scut.edu.cn [School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Tianhe District, Guangzhou 510641 (China)

    2017-01-15

    Highlights: • A mesostructured MFI zeolite was synthesized via dual-functional surfactant approach. • Mass transport was investigated by applying zero length column technique. • The catalyst exhibited excellent catalytic activity and long lifetime. • Gaussian DFT was employed to study the role of surfactant in crystallization process. - Abstract: A mesostructured ZSM-5 zeolite with multilamellar structure was successfully synthesized by employing a tetra-headgroup rigid bolaform quaternary ammonium surfactant. It was characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), nitrogen adsorption/desorption isotherms, amines temperature programmed desorption (amines-TPD), and computer simulation. These results indicated that the dual-functional amphiphilic surfactants play a critical role for directing the multilamellar structure with high mesoporosity. The mass transport and catalytic performances of the zeolite were investigated by zero length column (ZLC) technique and aldol condensation reactions to evaluate the structure-property relationship. These results clearly indicated that the mass transport of selected molecules in hierarchical zeolite can be accelerated by introducing mesoporous structure with mesostructure with reduced diffusion length and an overall enhanced resistance against deactivation in reactions involving large molecules. Furthermore, the dual-functional surfactant approach of making hierarchical zeolite with MFI nanosheets framework would open up new opportunities for design and synthesis of hierarchical zeolites with controllable mesoporous structures.

  20. Facile Synthesis of 3-Aryl-3-hydroxy-2-oxindoles from 2-Arylindoles

    Energy Technology Data Exchange (ETDEWEB)

    Moon, Hye Ran; Roh, Hwa Jung; Kim, Jae Nyoung [Chonnam National University, Gwangju (Korea, Republic of); Lee, Sangku [Korea Research Institute of Bioscience and Biotechnology, Chungju (Korea, Republic of)

    2016-07-15

    An efficient synthetic route of 3-aryl-3-hydroxy-2-oxindoles has been developed from 2-arylindoles. The procedure provides a brand-new synthetic method of 3-aryl-3-hydroxy-2-oxindoles from readily available starting materials in high yields. We reported an aerobic transition metal-free synthesis of 2,3-diarylindoles via an oxidative nucleophilic substitution of hydrogen (ONSH) pathway from 2-arylindoles and nitroarenes. As an example, the reaction of 2-phenylindole (1a) and 1,3-dinitrobenzene in DMSO in the presence of Cs{sub 2}CO{sub 3} under O{sub 2} balloon atmosphere afforded 2,3-diarylindole in good yield (78%) in short time, as shown in Scheme 1. During the study, we found the formation of 3-phenyl-3-hydroxy-2-oxindole (2a), albeit in moderate yield (41%), under the same reaction condition for a long time (8 h) without 1,3-dinitrobenzene. Based on the experimental results, the reaction mechanism for the conversion of 1a to 2a is proposed, as shown in Scheme 2. The indole anion I was converted to 3-hydroxyindolenine intermediate III via the hydroperoxide intermediate II. Subsequently, III was changed to an epoxide intermediate IV under basic condition, and a following semipinacol type rearrangement of IV would produce 3-phenyloxindole VI. A subsequent aerobic oxidation of VI would produce 2a.

  1. A Facile Solvothermal Method for Synthesis of CuInS2 Nanostructures

    Directory of Open Access Journals (Sweden)

    M. Mousavi-Kamazani

    2012-09-01

    Full Text Available CuInS2 nanostructures were  synthesized  via  a  simple  surfactant-free solvothermal  route.  In  this  synthesis,  thiosemicarbazide  and thioglycolic acid were used as sulfur sources. The effects of different parameters such as type of precursor and time on the morphology and particle  size  of  the  samples  have  been  investigated.  The nanostructures  were  characterized  by  means  of  X-ray  diffraction (XRD,  scanning  electron microscopy  (SEM,  energy-dispersive X- ray  analysis  (EDX,  Fourier  transform  infrared  (FT-IR  and photoluminescence  (PL  spectroscopy.  The  fill  factor  (FF,  open circuit voltage  (Voc, and  short circuit current  (Isc were obtained by I–V characterization.

  2. Facile synthesis of Curcuma longa tuber powder engineered metal nanoparticles for bioimaging applications

    Science.gov (United States)

    Sankar, Renu; Rahman, Pattanathu K. S. M.; Varunkumar, Krishnamoorthy; Anusha, Chidambaram; Kalaiarasi, Arunachalam; Shivashangari, Kanchi Subramanian; Ravikumar, Vilwanathan

    2017-02-01

    Nanomaterials based fluorescent agents are rapidly becoming significant and promising transformative tools for improving medical diagnostics for extensive in vivo imaging modalities. Compared with conventional fluorescent agents, nano-fluorescence has capabilities to improve the in vivo detection and enriched targeting efficiencies. In our laboratory we synthesized fluorescent metal nanoparticles of silver, copper and iron using Curcuma longa tuber powder by simple reduction. The physicochemical properties of the synthesized metal nanoparticles were attained using UV-visible spectrophotometry, scanning electron microscopy with EDAX spectroscopy, dynamic light scattering, Fourier-transform infrared spectroscopy and X-ray diffraction. The Curcuma longa tuber powder has one of the bioactive compound Curcumin might act as a capping agent during the synthesis of nanoparticles. The synthesized metal nanoparticles fluorescence property was confirmed by spectrofluorometry. When compared with copper and iron nanoparticles the silver nanoparticles showed high fluorescence intensity under spectrofluorometry. Moreover, in vitro cell images of the silver nanoparticles in A549 cell lines also correlated with the results of spectrofluorometry. These silver nanoparticles show inspiring cell-imaging applications. They enter into cells without any further modifications, and the fluorescence property can be utilized for fluorescence-based cell imaging applications.

  3. A facile synthesis of novel indole derivatives as potential antitubercular agents

    Directory of Open Access Journals (Sweden)

    Gulzar A. Khan

    2017-11-01

    Full Text Available A novel series of 5,5-dimethyl-11-phenyl-4b,5,5a,10,10a,11,11a,12-octahydro-10,11,12-triaza-indeno[2,1-b]fluorenes 3a–3l were prepared by reacting oxindole, aryl amines and acetone using dibutylamine as an organocatalyst via simultaneous Knoevenagel and Michael-type reactions. This preparation is environmentally benign, highly compatible and conveniently carried out in ethanol under mild conditions. The structures of the new compounds were determined by spectroscopic techniques, including IR, 1H NMR, 13C NMR and LCHRMS. Docking studies against an enoyl acyl carrier protein reductase predicted that the compounds possessed high binding affinity towards target molecules. The compound 3k (MIC, 40 μg/mL showed comparable activity with Isoniazid at the same concentrations against MT H37 Rv. Keywords: Green synthesis, Knoevenagel–Michael addition reaction, Dibutylamine, Antitubercular activity, Molecular docking

  4. Facile synthesis of porous TiO_2 photocatalysts using waste sludge as the template

    International Nuclear Information System (INIS)

    Wang, Xiaopeng; Huang, Shouqiang; Zhu, Nanwen; Lou, Ziyang; Yuan, Haiping

    2015-01-01

    Graphical abstract: Waste sludge is introduced to synthesize the waste sludge templated TiO_2 photocatalyst with porous structure, which possesses better photocatalytic activity compared to pure TiO_2. - Highlights: • Waste sludge is introduced to synthesize the TiO_2 photocatalyst. • Waste sludge templated TiO_2 sample possesses porous structure. • Waste sludge templated TiO_2 sample exhibits high photocatalytic activity. - Abstract: A resource utilization method of waste sludge is present by the synthesis of waste sludge templated TiO_2 photocatalysts. The organic materials in waste sludge are used as the pore-forming agents, and the transition metals included in the remaining waste sludge through calcination (WSC) can serve as the dopants for the WSC-TiO_2 (WSCT) photocatalyst. The visible and UV–visible light driven photocatalytic activities of WSCT are much better compared to those of pure TiO_2 and WSC, and it is originated from the higher light absorption property and the efficient electron–hole pair separation provided by waste sludge.

  5. Facile synthesis, structure, and properties of Ag{sub 2}S/Ag heteronanostructure

    Energy Technology Data Exchange (ETDEWEB)

    Sadovnikov, S. I., E-mail: sadovnikov@ihim.uran.ru; Gusev, A. I. [Ural Branch of the Russian Academy of Sciences, Institute of Solid State Chemistry (Russian Federation)

    2016-09-15

    Ag{sub 2}S/Ag heteronanostructure has been produced by a simple one-stage chemical deposition from aqueous solutions of silver nitrate, sodium sulfide, and sodium citrate with the use of monochromatic light irradiation. For simultaneous synthesis of Ag{sub 2}S and Ag nanoparticles, deposition has been performed from reaction mixtures with reduced sodium sulfide concentration. The size of Ag{sub 2}S and Ag nanoparticles is 45–50 and 15–20 nm, respectively. It is established that in the contact layer between silver sulfide and silver, nonconducting α-Ag{sub 2}S acanthite transforms into superionic β-Ag{sub 2}S argentite under the action of external electric field. The scheme of the operation of a resistive switch based on an Ag{sub 2}S/Ag heteronanostructure is proposed. The UV–Vis optical absorption spectra of colloidal solutions of Ag{sub 2}S/Ag heteronanostructures have been studied.Graphical Abstract.

  6. Facile synthesis of mesostructured ZSM-5 zeolite with enhanced mass transport and catalytic performances

    International Nuclear Information System (INIS)

    Li, Chao; Ren, Yanqun; Gou, Jinsheng; Liu, Baoyu; Xi, Hongxia

    2017-01-01

    Highlights: • A mesostructured MFI zeolite was synthesized via dual-functional surfactant approach. • Mass transport was investigated by applying zero length column technique. • The catalyst exhibited excellent catalytic activity and long lifetime. • Gaussian DFT was employed to study the role of surfactant in crystallization process. - Abstract: A mesostructured ZSM-5 zeolite with multilamellar structure was successfully synthesized by employing a tetra-headgroup rigid bolaform quaternary ammonium surfactant. It was characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), nitrogen adsorption/desorption isotherms, amines temperature programmed desorption (amines-TPD), and computer simulation. These results indicated that the dual-functional amphiphilic surfactants play a critical role for directing the multilamellar structure with high mesoporosity. The mass transport and catalytic performances of the zeolite were investigated by zero length column (ZLC) technique and aldol condensation reactions to evaluate the structure-property relationship. These results clearly indicated that the mass transport of selected molecules in hierarchical zeolite can be accelerated by introducing mesoporous structure with mesostructure with reduced diffusion length and an overall enhanced resistance against deactivation in reactions involving large molecules. Furthermore, the dual-functional surfactant approach of making hierarchical zeolite with MFI nanosheets framework would open up new opportunities for design and synthesis of hierarchical zeolites with controllable mesoporous structures.

  7. Facile synthesis and characterization of novel biodegradable amphiphilic block copolymers bearing pendant hydroxyl groups

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Gaicen; Fan, Xiaoshan; Xu, Bingcan; Zhang, Delong; Hu, Zhiguo, E-mail: zghu@htu.cn

    2014-10-01

    Novel amphiphilic block copolymers bearing pendant hydroxyl groups polylactide-b–poly(3,3-bis(Hydroxymethyl–triazolylmethyl) oxetane)-b–polylactide (PLA-b–PHMTYO-b–PLA) were synthesized via a facile and efficient method. First, the block copolymer intermediates polylactide-b–poly(3,3-Diazidomethyloxetane)-b–polylactide (PLA-b–PBAMO-b–PLA) were synthesized through ring-opening polymerization of lactide using PBAMO as a macroinitiator. Following “Click” reaction of PLA-b–PBAMO-b–PLA with propargyl alcohol provided the targeted amphiphilic block copolymers PLA-b–PHMTYO-b–PLA with pendant hydroxyl groups. The composition and structure of prepared copolymers were characterized by {sup 1}H nuclear magnetic resonance ({sup 1}H NMR) spectroscopy, Fourier transform infrared (FT-IR) and gel permeation chromatography (GPC). The self-assembly behavior of the copolymers in water was investigated by transmission electron microscope (TEM), dynamic light scattering (DLS) and static light scattering (SLS). The results showed that the novel copolymers PLA-b–PHMTYO-b–PLA self-assembled into spherical micelles with diameters ranging from 100 nm to 200 nm in aqueous solution. These copolymers also exhibited low critical micellar concentrations (CMC: 6.9 × 10{sup −4} mg/mL and 3.9 × 10{sup −5} mg/mL, respectively). In addition, the in vitro cytotoxicity of these copolymers was determined in the presence of L929 cells. The results showed that the block copolymers PLA-b–PHMTYO-b–PLA exhibited better biocompatibility. Therefore, these well-defined copolymers are expected to find some applications in drug delivery or tissue engineering. - Highlights: • The method to synthesize PLA-b–PHMTYO-b–PLA is relatively facile and efficient. • PLA-b–PHMTYO-b–PLA self-assembles into spherical micelles with low CMC in water. • PLA-b–PHMTYO-b–PLA exhibits better biocompatibility and biodegradability.

  8. Facile Synthesis of Porous ZnMnO3 Spherulites with a High Lithium Storage Capability

    International Nuclear Information System (INIS)

    Liu, Xinru; Zhao, Chenhao; Zhang, He; Shen, Qiang

    2015-01-01

    Graphical abstract: Porous ZnMnO 3 spherulites show an enhanced high lithium storage capability when potentially applied as a lithium-ion battery anode for the first time. - Highlights: • Composite Zn 0.5 Mn 0.5 CO 3 microspheres are facilely co-precipitated. • Porous ZnMnO 3 spherulites can be used as a lithium-ion battery anode. • Porous ZnMnO 3 spherulites show superior electrochemical properties. • A synergistic effect of Zn-O and Mn-O components in cubic ZnMnO 3 is proposed. - Abstract: In this paper, pure-phase ZnMnO 3 porous spherulites are uniquely synthesized through the thermal decomposition of Zn-Mn binary carbonate precursors facilely co-precipitated at room temperature, possessing an average diameter of 1.2 ± 0.3 μm and acquiring porosity with a specific surface area of 24.3 m 2 g −1 . When tentatively applied as lithium-ion battery anodes for the first time, these porous spherulites deliver an initial discharge capacity of 1294 mAh g −1 at 500 mA g −1 and retain an reversible value of 879 mAh g −1 over 150 cycles. By comparison, the equimolar powder mixture of nano-sized ZnO and MnO 2 synergistically shows a higher lithium storage capability than the two unary transition metal oxides, but lower than anode material ZnMnO 3 . Aside from its nanostructured characteristics, an inner atomic synergistic effect within the cubic lattices may account for the superior electrochemical performance of well-crystallized ZnMnO 3

  9. Facile synthesis and characterization of novel biodegradable amphiphilic block copolymers bearing pendant hydroxyl groups

    International Nuclear Information System (INIS)

    Hu, Gaicen; Fan, Xiaoshan; Xu, Bingcan; Zhang, Delong; Hu, Zhiguo

    2014-01-01

    Novel amphiphilic block copolymers bearing pendant hydroxyl groups polylactide-b–poly(3,3-bis(Hydroxymethyl–triazolylmethyl) oxetane)-b–polylactide (PLA-b–PHMTYO-b–PLA) were synthesized via a facile and efficient method. First, the block copolymer intermediates polylactide-b–poly(3,3-Diazidomethyloxetane)-b–polylactide (PLA-b–PBAMO-b–PLA) were synthesized through ring-opening polymerization of lactide using PBAMO as a macroinitiator. Following “Click” reaction of PLA-b–PBAMO-b–PLA with propargyl alcohol provided the targeted amphiphilic block copolymers PLA-b–PHMTYO-b–PLA with pendant hydroxyl groups. The composition and structure of prepared copolymers were characterized by 1 H nuclear magnetic resonance ( 1 H NMR) spectroscopy, Fourier transform infrared (FT-IR) and gel permeation chromatography (GPC). The self-assembly behavior of the copolymers in water was investigated by transmission electron microscope (TEM), dynamic light scattering (DLS) and static light scattering (SLS). The results showed that the novel copolymers PLA-b–PHMTYO-b–PLA self-assembled into spherical micelles with diameters ranging from 100 nm to 200 nm in aqueous solution. These copolymers also exhibited low critical micellar concentrations (CMC: 6.9 × 10 −4 mg/mL and 3.9 × 10 −5 mg/mL, respectively). In addition, the in vitro cytotoxicity of these copolymers was determined in the presence of L929 cells. The results showed that the block copolymers PLA-b–PHMTYO-b–PLA exhibited better biocompatibility. Therefore, these well-defined copolymers are expected to find some applications in drug delivery or tissue engineering. - Highlights: • The method to synthesize PLA-b–PHMTYO-b–PLA is relatively facile and efficient. • PLA-b–PHMTYO-b–PLA self-assembles into spherical micelles with low CMC in water. • PLA-b–PHMTYO-b–PLA exhibits better biocompatibility and biodegradability

  10. Facile synthesis of reduced graphene oxide/CoWO4 nanocomposites with enhanced electrochemical performances for supercapacitors

    International Nuclear Information System (INIS)

    Xu, Xiaowei; Shen, Jianfeng; Li, Na; Ye, Mingxin

    2014-01-01

    Highlights: • RGO/CoWO 4 composites were successfully prepared through a facile hydrothermal method. • RGO/CoWO 4 composites show much higher specific capacitances than pure CoWO 4 . • Enhanced electrical conductivity leads to superior electrochemical performance. - Abstract: A facile one-pot hydrothermal method was provided for synthesis of the reduced graphene oxide-cobalt tungstate (RGO/CoWO 4 ) nanocomposites with the enhanced electrochemical performances for supercapacitors for the first time. The resulting nanocomposites are comprised of CoWO 4 nanospheres that are well-anchored on graphene sheets by in situ reducing. The prepared RGO/CoWO 4 nanocomposites have been thoroughly characterized by Fourier–transform infrared spectroscopy, X-ray diffraction, Raman spectroscopy, Thermogravimetric analysis, Scanning electron microscopy, Transmission electron microscopy, X-ray photoelectron spectroscopy, and N 2 adsorption–desorption. Importantly, the prepared nanocomposites exhibit superior electrochemical performance to CoWO 4 as electrodes for supercapacitors. As a result, RGO/CoWO 4 nanocomposites with 91.6 wt% CoWO 4 content achieved a specific capacitance about 159.9 F g −1 calculated from the CV curves at 5 mV s −1 , which was higher than that of CoWO 4 (60.6 F g −1 ). The good electrochemical performance can be attributed to the increased electrical conductivity and the creation of new active sites due to the synergetic effect of RGO and CoWO 4 nanospheres. The cyclic stability tests demonstrated capacitance retention of about 94.7% after 1000 cycles, suggesting the potential application of RGO/CoWO 4 nanocomposites in energy-storage devices

  11. Facile synthesis, characterization and catalytic function of gelatin stabilized gold nanoparticles

    International Nuclear Information System (INIS)

    Tagar, Z.A.; Sirajuddin, A.; Memon, N.; Kalwar, H.; Junejo, Y.; Hassan, S.S.

    2012-01-01

    In the present investigation, we report a new one phase, one pot method for synthesis of 3.5 :t 0.7 nm average sized gelatin capped gold nano particles (Gel-AuNPs) using strong reductant NaBH/sub 4/ in aqueous system at room temperature. Size controlled Gel-AuNPs were characterized by UV-Visible, STEM, XRD, DLS and Ff -IR. Spherical Gel-AuNPs showed excellent catalytic activity for reduction of three differently charged dyes eosin B (EB), methylene blue (MB) and rose Bengal (RB) in the presence of NaBH/sub 4/. The study revealed that 100% reduction of EB, MB and RB dyes was carried out in just 150 sec. The developed catalyst was easy to recover and capable to be reused three times. The process of reduction rate and kinetics of dyes was monitored using UV-Visible spectrophotometer. A plot of InC V s time (sec) showed that reaction follows the first order kinetics. Rate constant (K) was determined for EB, MB and RB reduction at 10 I.LM, which was found as 2.735 x10-2 sec/sup -1/, 2.738 x 10/sup -2/ sec/sup -1/ and 2.55 x 10/sup -2/ sec/sup -1/, respectively. The study revealed that catalytic reduction of dyes by Gel-AuNPs in aqueous medium is environmental friendly in terms of recovery of catalyst, is exceptionally fast and hence extremely economical. (author)

  12. Facile synthesis of palladium nanoparticle doped polyaniline nanowires in soft templates for catalytic applications

    Science.gov (United States)

    Kshirasagar, Krushna J.; Markad, Uddhav S.; Saha, Abhijit; Sharma, Kiran Kumar K.; Sharma, Geeta K.

    2017-02-01

    Palladium nanoparticles doped polyaniline (Pd-PANI) nanocomposite (NCs) is synthesized in surfactant based liquid crystalline mesophase by chemical oxidation followed by radiolysis. The confinement of the liquid crystalline mesophase facilitates polymerization of aniline monomers and their 1D growth into polyaniline (PANI) nanowires by using ammonium persulfate. The PANI nanowires have an average diameter of 30-40 nm. The in situ radiolytic reduction of palladium ions ensures uniform size distribution of the palladium (Pd) nanoparticles on the surface of the PANI nanowires. The synthesized Pd-PANI nanocomposites show wire like structures of PANI (diameter ~30-40 nm) on which Pd nanoparticles of the size 10 nm are decorated. The identical average diameter of the PANI nanowires before and post gamma irradiation suggest high stability of the PANI nanowires in liquid crystalline mesophase. Surface characterization of the NCs were carried out using BET and XPS. The catalytic activity of Pd-PANI NCs are investigated in the reduction of methylene blue (MB) and 4-nitro phenol (4-NP) by sodium borohydride (NaBH4). The kinetics of the Pd-PANI NCs catalysed reactions are analysed using the Langmuir-Hinshelwood model. The apparent rate constant (k app) for the MB and 4-NP reduction reactions is 29  ×  10-3 s-1 and 20  ×  10-3 s-1 respectively with an actual Pd catalyst loading of 2.665  ×  10-4 ppm. Further, the recyclability of the Pd-PANI NCs catalyst in both the reduction reactions shows the stability of the catalyst up to four reaction cycles tested in this investigation and the multifunctional nature of the catalyst. The study provides a new approach for the directional synthesis of conducting polymer-metal nanocomposites and their possible application as a nanocatalyst in environmental remediation.

  13. Facile synthesis, single crystal analysis, and computational studies of sulfanilamide derivatives

    Science.gov (United States)

    Tahir, Muhammad Nawaz; Khalid, Muhammad; Islam, Ayesha; Ali Mashhadi, Syed Muddassir; Braga, Ataualpa A. C.

    2017-01-01

    Antibacterial resistance is a worldwide problem. Sulfanilamide is widely used antibacterial. For the first time, we report here a simple method for the derivative synthesis of the title drugs, single crystal XRD and density functional theory (DFT) studies. The optimized molecular structure, natural bond orbital (NBO), frontier molecular orbitals (FMOs) molecular electrostatic potential studies (MEP) and Mulliken population analysis (MPA) have been performed using M06-2X/6-31G(d, p). The FT-IR spectra and thermodynamic parameters were calculated at M06-2X/6-311 + G(2d,p) and B3LYP/6-31G(d, p) levels respectively, while, the UV-Vis analysis was performed using TD-DFT/B3LYP/6-31G(d, p) method. The experimental FT-IR spectra of both compounds were also carried out to reconfirm sbnd H⋯Osbnd hydrogen bonds. The DFT optimized parameters exhibiting good agreement with the experimental data. NBO analysis explored the hyper conjugative interaction and stability of title crystals, especially, reconfirmed the existence of sbnd H⋯Osbnd hydrogen bonds between the dimers. The FT-IR, thermodynamic parameters, MEP and MPA also revealed the hydrogen bonding detail is harmonious to XRD data. As a matter of the fact, the hydrogen bonding is a significant parameter for the understanding and design of molecular crystals, subsequently; it can also play a vital role in the supramolecular chemistry. Moreover, the global reactivity descriptors suggest that title compounds might be bioactive.

  14. Facile synthesis of flower like copper oxide and their application to hydrogen peroxide and nitrite sensing

    Directory of Open Access Journals (Sweden)

    Zhang Li

    2011-12-01

    Full Text Available Abstract Background The detection of hydrogen peroxide (H2O2 and nitrite ion (NO2- is of great important in various fields including clinic, food, pharmaceutical and environmental analyses. Compared with many methods that have been developed for the determination of them, the electrochemical detection method has attracted much attention. In recent years, with the development of nanotechnology, many kinds of micro/nano-scale materials have been used in the construction of electrochemical biosensors because of their unique and particular properties. Among these catalysts, copper oxide (CuO, as a well known p-type semiconductor, has gained increasing attention not only for its unique properties but also for its applications in many fields such as gas sensors, photocatalyst and electrochemistry sensors. Continuing our previous investigations on transition-metal oxide including cuprous oxide and α-Fe2O3 modified electrode, in the present paper we examine the electrochemical and electrocatalytical behavior of flower like copper oxide modified glass carbon electrodes (CuO/GCE. Results Flower like copper oxide (CuO composed of many nanoflake was synthesized by a simple hydrothermal reaction and characterized using field-emission scanning electron microscopy (FE-SEM and X-ray diffraction (XRD. CuO modified glass carbon electrode (CuO/GCE was fabricated and characterized electrochemically. A highly sensitive method for the rapid amperometric detection of hydrogen peroxide (H2O2 and nitrite (NO2- was reported. Conclusions Due to the large specific surface area and inner characteristic of the flower like CuO, the resulting electrode show excellent electrocatalytic reduction for H2O2 and oxidation of NO2-. Its sensitivity, low detection limit, fast response time and simplicity are satisfactory. Furthermore, this synthetic approach can also be applied for the synthesis of other inorganic oxides with improved performances and they can also be extended to

  15. A facile synthesis method of hydroxyethyl cellulose-silver nanoparticle scaffolds for skin tissue engineering applications.

    Science.gov (United States)

    Zulkifli, Farah Hanani; Hussain, Fathima Shahitha Jahir; Zeyohannes, Senait Sileshi; Rasad, Mohammad Syaiful Bahari Abdull; Yusuff, Mashitah M

    2017-10-01

    Green porous and ecofriendly scaffolds have been considered as one of the potent candidates for tissue engineering substitutes. The objective of this study is to investigate the biocompatibility of hydroxyethyl cellulose (HEC)/silver nanoparticles (AgNPs), prepared by the green synthesis method as a potential host material for skin tissue applications. The substrates which contained varied concentrations of AgNO 3 (0.4%-1.6%) were formed in the presence of HEC, were dissolved in a single step in water. The presence of AgNPs was confirmed visually by the change of color from colorless to dark brown, and was fabricated via freeze-drying technique. The outcomes exhibited significant porosity of >80%, moderate degradation rate, and tremendous value of water absorption up to 1163% in all samples. These scaffolds of HEC/AgNPs were further characterized by SEM, UV-Vis, ATR-FTIR, TGA, and DSC. All scaffolds possessed open interconnected pore size in the range of 50-150μm. The characteristic peaks of Ag in the UV-Vis spectra (417-421nm) revealed the formation of AgNPs in the blend composite. ATR-FTIR curve showed new existing peak, which implies the oxidation of HEC in the cellulose derivatives. The DSC thermogram showed augmentation in T g with increased AgNO 3 concentration. Preliminary studies of cytotoxicity were carried out in vitro by implementation of the hFB cells on the scaffolds. The results substantiated low toxicity of HEC/AgNPs scaffolds, thus exhibiting an ideal characteristic in skin tissue engineering applications. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Recovery Act: Oxy-Combustion Technology Development for Industrial-Scale Boiler Applications. Task 4 - Testing in Alstom's 15 MWth Boiler Simulation Facility

    Energy Technology Data Exchange (ETDEWEB)

    Levasseur, Armand

    2014-04-30

    Alstom Power Inc. (Alstom), under U.S. DOE/NETL Cooperative Agreement No. DE-NT0005290, is conducting a development program to generate detailed technical information needed for application of oxy-combustion technology. The program is designed to provide the necessary information and understanding for the next step of large-scale commercial demonstration of oxy combustion in tangentially fired boilers and to accelerate the commercialization of this technology. The main project objectives include: Design and develop an innovative oxyfuel system for existing tangentially-fired boiler units that minimizes overall capital investment and operating costs; Evaluate performance of oxyfuel tangentially fired boiler systems in pilot scale tests at Alstom’s 15 MWth tangentially fired Boiler Simulation Facility (BSF); Address technical gaps for the design of oxyfuel commercial utility boilers by focused testing and improvement of engineering and simulation tools; Develop the design, performance and costs for a demonstration scale oxyfuel boiler and auxiliary systems; Develop the design and costs for both industrial and utility commercial scale reference oxyfuel boilers and auxiliary systems that are optimized for overall plant performance and cost; and, Define key design considerations and develop general guidelines for application of results to utility and different industrial applications. The project was initiated in October 2008 and the scope extended in 2010 under an ARRA award. The project is scheduled for completion by April 30, 2014. Central to the project is 15 MWth testing in the BSF, which provided in-depth understanding of oxy-combustion under boiler conditions, detailed data for improvement of design tools, and key information for application to commercial scale oxy-fired boiler design. Eight comprehensive 15 MWth oxy-fired test campaigns were performed with different coals, providing detailed data on combustion, emissions, and thermal behavior over a matrix of

  17. Facile synthesis of porous graphene as binder-free electrode for supercapacitor application

    Energy Technology Data Exchange (ETDEWEB)

    Luo, Guangsheng [Nanjing National Laboratory of Microstructures and Department of Physics, Jiangsu Key Laboratory for Nanotechnology, Nanjing University, Nanjing 210093 (China); Academy of Space Technolgy, Nanchang University, Nanchang, Jiangxi 330031 (China); Huang, Haifu, E-mail: haifuh@gmail.com [Nanjing National Laboratory of Microstructures and Department of Physics, Jiangsu Key Laboratory for Nanotechnology, Nanjing University, Nanjing 210093 (China); College of Physics Science and Engineering, Guangxi University, Nanning 530004 (China); Lei, Chenglong; Cheng, Zhenzhi; Wu, Xiaoshan [Nanjing National Laboratory of Microstructures and Department of Physics, Jiangsu Key Laboratory for Nanotechnology, Nanjing University, Nanjing 210093 (China); Tang, Shaolong, E-mail: tangsl@nju.edu.cn [Nanjing National Laboratory of Microstructures and Department of Physics, Jiangsu Key Laboratory for Nanotechnology, Nanjing University, Nanjing 210093 (China); Du, Youwei [Nanjing National Laboratory of Microstructures and Department of Physics, Jiangsu Key Laboratory for Nanotechnology, Nanjing University, Nanjing 210093 (China)

    2016-03-15

    Graphical abstract: - Highlights: • Our results provide a facile method to fabricate a binder-free porous rGO electrode for supercapacitors. • Polystyrene (PS) colloidal particles were used as spacers to prepare high-performance porous grapheme deposited directly on Ni foam substrate. • The specific capacitance of the rGO/NF electrode decreased by 7% after 2000 cycles and high rate capability of 53% capacitance retention at 100 A g{sup −1}. - Abstract: Here, porous grapheme oxide (GO) gel deposited on nickel foam was prepared by using polystyrene (PS) colloidal particles as spacers for use as electrodes in high rate supercapacitors, then reduced by Vitamin C aqueous solution in ambient condition. The PS particles were surrounded by reduced graphene oxide (rGO) sheets, forming crinkles and rough textures. When PS particles were selectively removed, rGO gel coated on the skeleton of Ni foam can formed an open porous structure, which prevents elf-aggregation and restacking of graphene sheets. The porous rGO-based supercapacitors exhibit excellent electrochemical performances such as a specific capacitance of 152 F g{sup −1} at 1 A g{sup −1}, high rate capability of 53% capacitance retention upon a current increase to 100 A g{sup −1} and good cycle stability, due to effective rapid and short pathways for ionic and electronic transport provided by the sub-micrometer structure of rGO gel and 3D interconnected network of Ni foam.

  18. Facile synthesis of surface-functionalized magnetic nanocomposites for effectively selective adsorption of cationic dyes

    Science.gov (United States)

    Hua, Yani; Xiao, Juan; Zhang, Qinqin; Cui, Chang; Wang, Chuan

    2018-04-01

    A new magnetic nano-adsorbent, polycatechol modified Fe3O4 magnetic nanoparticles (Fe3O4/PCC MNPs) were prepared by a facile chemical coprecipitation method using iron salts and catechol solution as precursors. Fe3O4/PCC MNPs owned negatively charged surface with oxygen-containing groups and showed a strong adsorption capacity and fast adsorption rates for the removal of cationic dyes in water. The adsorption capacity of methylene blue (MB), cationic turquoise blue GB (GB), malachite green (MG), crystal violet (CV) and cationic pink FG (FG) were 60.06 mg g- 1, 70.97 mg g- 1, 66.84 mg g- 1, 66.01 mg g- 1 and 50.27 mg g- 1, respectively. The adsorption mechanism was proposed by the analyses of the adsorption isotherms and adsorption kinetics of cationic dyes on Fe3O4/PCC MNPs. Moreover, the cationic dyes adsorbed on the MNPs as a function of contact time, pH value, temperature, coexisting cationic ions and ion strength were also investigated. These results suggested that the Fe3O4/PCC MNPs is promising to be used as a magnetic adsorbent for selective adsorption of cationic dyes in wastewater treatment.

  19. Facile hydrothermal synthesis of one-dimensional nanostructured α-MnO2 for supercapacitors

    Science.gov (United States)

    Wei, Hongmei; Wang, Jinxing; Yang, Shengwei; Zhang, Yangyang; Li, Tengfei; Zhao, Shuoqing

    2016-09-01

    α-MnO2 recently becomes a promising candidate of electrode materials for high effective supercapacitors in which it possesses of unique structure of 2×2 tunnels that can provide more electrons and ions diffusion paths. In this work, different morphologies MnO2 with α-phase crystalline structure have been prepared via a one-step facile hydrothermal method by adding various reagents. Compositions, microstructures and morphologies of these as-synthesized materials were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) and electrochemical properties of α-MnO2 electrodes were studied by the cyclic voltammetry (CV), galvanostatic charge/discharge and electrochemical impedance spectroscopy (EIS) in 1 M Na2SO4 aqueous solution. The specific capacitance of nanowires were 158 F g-1 while the specific capacitance of nanorods were 106 F g-1 at current density of 4 A g-1, and improved performance of the wire-like electrode material was probably ascribed to the larger specific surface area that can provide relatively more active sites for high capacity. Meanwhile, both the nanowires and nanorods of MnO2 presented fine cycle stability after continuous multiple charge/discharge times.

  20. Facile synthesis of conjugated polymeric Schiff base as negative electrodes for lithium ion batteries

    International Nuclear Information System (INIS)

    Ye, Haijun; Jiang, Fangqing; Li, Hongqin; Xu, Zheng; Yin, Jiao; Zhu, Hui

    2017-01-01

    Graphical abstract: Polymeric Schiff base (PSB) exhibits a stable cyclability as an organic Li-ion battery anode Display Omitted -- Highlights: •A conjugated Schiff base polymer has been synthesized by a solid-phase reaction. •The polymer suppresses the dissolution of organic monomer into the organic electrolyte. •The polymer demonstrates high reversible capacity and excellent cyclic performance. -- Abstract: The redox-active organic compounds show great potentials as anodes for high energy density Li-ion batteries (LIBs), comparing with the traditional transition metal-based inorganic compounds. However, the inevitable dissolution behaviors of these organics in organic electrolyte will arouse the recession in their cycling stabilities. To circumvent this problem, we successfully applied an electrochemically active imine group to connect the carbonyl compound to form conjugated polymer, where the occurrence of multi-electron reactions suppressed the dissolution of anthraquinone in the organic electrolyte with improved cycling stability and high capacity for LIBs. In detail, by virtue of a facile solid-phase reaction between 1, 4-diaminoanthraquinone (14DAAQ) and p-phthalaldehyde (PPD), a highly conjugated polymeric Schiff base (PSB) was synthesized. The obtained PSB exhibited a reversible specific capacity of 175 mAh g −1 at a current density of 10 mA g −1 . In addition, after 100 cycles, a cycling stability with 90% capacity retention can be maintained, manifesting a promising application of the organic material in high performance anodes for LIBs.

  1. Facile synthesis of S, N co-doped carbon dots and investigation of their photoluminescence properties.

    Science.gov (United States)

    Zhang, Yue; He, Junhui

    2015-08-21

    A facile one-pot approach to prepare photoluminescent carbon dots (CDs) was developed through hydrothermal treatment of cysteine and citric acid. The obtained CDs show stable and bright blue emission with a quantum yield of 54% and an average lifetime of 11.61 ns. Moreover, the two-photon induced upconversion fluorescence of the CDs was observed and demonstrated. Interestingly, both down and up conversion fluorescence of the CDs show excitation-independent emission, which is quite different from most of the previously reported CDs. Ultrafast spectroscopy was also employed here to study the photoluminescence (PL) properties of the CDs. After characterization using various spectroscopic techniques, a unique PL mechanism for the as-prepared CDs' fluorescence was proposed accordingly. In addition, the influence of various metal ions on the CD fluorescence was examined and no quenching phenomena were observed. Meanwhile, gold nanoparticles (Au NPs) were found to be good quenchers of CD fluorescence and their quenching behavior was fitted to the Stern-Volmer equation. This provides new opportunities for fluorescence sensor designs and light energy conversion applications. Finally, the as-prepared CDs were inkjet-printed to form a desirable pattern, which is useful for fluorescent patterns, and anti-counterfeiting labeling.

  2. Facile synthesis and characterization of hexagonal NbSe2 nanoplates

    International Nuclear Information System (INIS)

    Zhang, Xianghua; Zhang, Du; Tang, Hua; Ji, Xiaorui; Zhang, Yi; Tang, Guogang; Li, Changsheng

    2014-01-01

    Graphical abstract: - Highlights: • Uniform hexagonal NbSe 2 nanoplates were prepared by a simple solid state reaction. • The possible formation mechanism of the NbSe 2 nanoplates was discussed. • The formation of NbSe 2 nanoplates undergoes a series of phase transition. - Abstract: The NbSe 2 nanoplates with hexagonal morphology have been successfully prepared by a facile, environmentally friendly reaction in closed reactor at moderate temperature. The thermal (750 °C) solid-state reaction between the ball-milled mixture of micro-sized Nb and Se yielded a high yield of NbSe 2 nanoplates. The as-prepared products were characterized by XRD, EDS, and SEM. The results showed that the as-prepared products were hexagonal phase NbSe 2 nanoplates with uniform sizes and the formation of NbSe 2 nanoplates underwent a series of phase transition. On the basis of experimental results obtained at different temperatures, a reasonable reaction process and a formation mechanism were proposed. Moreover, the ball milling time played a crucial role in acquiring the homogeneous distribution nanoplates

  3. Novel Mesoporous Flowerlike Iron Sulfide Hierarchitectures: Facile Synthesis and Fast Lithium Storage Capability

    Directory of Open Access Journals (Sweden)

    Quanning Ma

    2017-12-01

    Full Text Available The 3D flowerlike iron sulfide (F-FeS is successfully synthesized via a facile one-step sulfurization process, and the electrochemical properties as anode materials for lithium ion batteries (LIBs are investigated. Compared with bulk iron sulfide, we find that the unique structural features, overall flowerlike structure, composed of several dozen nanopetals and numerous small size iron sulfide particles embedded within the fine nanopetals, and hierarchical pore structure features provide signification improvements in lithium storage performance, with a high-rate discharge capacity of 779.0 mAh g−1 at a rate of 5 A g−1, due to effectively alleviating the volume expansion during the lithiation/delithiation process, and shorting the diffusion length of both lithium ion and electron. Especially, an excellent cycling stability are achieved, a high discharge capacity of 890 mAh g−1 retained at a rate of 1.0 A g−1, suggesting its promising applications in lithium ion batteries (LIBs.

  4. Facile synthesis of porous Pt botryoidal nanowires and their electrochemical properties

    International Nuclear Information System (INIS)

    Huang, Zhongyuan; Zhou, Haihui; Chen, Zhongxue; Zeng, Fanyan; Chen, Liang; Luo, Wucheng; Kuang, Yafei

    2014-01-01

    Highlights: • Porous Pt nanowires were synthesized by combination of soft and hard templets. • Te nanowires were used as the hard templet and reductant. • The Pt nanowires are composed of many small Pt nanoparticles and pores. • The Pt nanowires have very good electrochemical activity and stability. - Abstract: Long and porous Pt botryoidal nanowires (Pt BNWs) were facilely synthesized by combination of soft and hard templates accompanying chemical reduction of ascorbic acid and replacement of Te nanowires. This bis-template and bis-reductant method is proved to be an effective way to prepare nanowires with special structure. The scanning electron microscopy and transmission electron microscopy images show the as-prepared product is botryoidal nanowires with diameter of 20–30 nm and length of several micrometers. High resolution transmission electron microscopy shows the Pt botryoidal nanowires are composed of many small Pt nanoparticles (about 3 nm in diameter), which is just like that many grapes grow on the branch. These small nanoparticles make Pt nanowires have botryoidal and porous structure. Moreover, the diameter of Pt BNWs can be adjusted by changing the dosage of Pt precursor, polyvinylpyrrolidone and L-ascorbic acid. The electrocatalytic performance of Pt botryoidal nanowires is studied, which shows that the as-prepared Pt botryoidal nanowires have not only high activity but also good stability for oxygen reduction reaction

  5. Facile synthesis of magnetic Fe3O4/graphene composites for enhanced U(VI) sorption

    Science.gov (United States)

    Zhao, Donglin; Zhu, Hongyu; Wu, Changnian; Feng, Shaojie; Alsaedi, Ahmed; Hayat, Tasawar; Chen, Changlun

    2018-06-01

    A novel magnetic Fe3O4/graphene composite (FGC) was fabricated by a facile one-step reaction route and shown to be effective for sorbing U(VI) from aqueous solution. The structure, properties and application of the prepared FGC composite were well evaluated. The high saturation magnetization (45.6 emu/g) made FGC easier to be separated from the media within several seconds under an external magnetic. Effects of different ambient conditions (i.e., pH and ionic strength, contact time, temperatures) on sorption behaviors of U(VI) on FGC were carried out by batch experiments. According to the calculation of Langmuir model, the maximum sorption capacity of U(VI) on the FGC at pH 5.5 and 298 K was 176.47 mg/g. The sorption was correlated with the effects of pH, contact time, and temperature. X-ray photoelectron spectroscopy analysis revealed that U(VI) was sorbed on FGC via oxygen-containing functional groups. This work demonstrated that FGC could be recycled and used as an effective recyclable sorbent for sorption of U(VI).

  6. Facile synthesis and excellent microwave absorption properties of FeCo-C core-shell nanoparticles

    Science.gov (United States)

    Liang, Bingbing; Wang, Shiliang; Kuang, Daitao; Hou, Lizhen; Yu, Bowen; Lin, Liangwu; Deng, Lianwen; Huang, Han; He, Jun

    2018-02-01

    FeCo-C core-shell nanoparticles (NPs) with diameters of 10-50 nm have been fabricated on a large scale by one-step metal-organic chemical vapor deposition using the mixture of cobalt acetylacetonate and iron acetylacetonate as the precursor. The Fe/Co molar ratio of the alloy nanocores and graphitization degree of C shells, and thus the magnetic and electric properties of the core-shell NPs, can be tuned by the deposition temperature ranging from 700 °C to 900 °C. Comparative tests reveal that a relatively high Fe/Co molar ratio and low graphitization degree benefit the microwave absorption (MA) performance of the core-shell NPs. The composite with 20 wt% core-shell NP obtained at 800 °C and 80 wt% paraffin exhibits an optimal reflection loss ({{R}}{{L}}) of -60.4 dB at 7.5 GHz with a thickness of 3.3 mm, and an effective absorption bandwidth (frequency range for RL ≤10 dB) of 9.2 GHz (8.8-18.0 GHz) under an absorber thickness of 2.5 mm. Our study provides a facile route for the fabrication of alloy-C core-shell nanostructures with high MA performance.

  7. Facile synthesis of mesoporous silica sublayer with hierarchical pore structure on ceramic membrane using anionic polyelectrolyte.

    Science.gov (United States)

    Kang, Taewook; Oh, Seogil; Kim, Honggon; Yi, Jongheop

    2005-06-21

    A facile method for introducing mesoporous silica sublayer onto the surface of a ceramic membrane for use in liquid-phase separation is described. To reduce the electrostatic repulsion between the mesoporous silica sol and the ceramic membrane in highly acidic conditions (pH ceramic membrane, as confirmed by experimental titration data. Consistent with the titration results, the amount of mesoporous silica particles on the surface of the ceramic membrane was low, in the absence of PSS- treatment, whereas mesoporous silica sublayer with hierarchical pore structure was produced, when 1 wt % PSS- was used. The results show that mesoporous silica grows in the confined surface, eventually forming a multistacked surface architecture. The mesoporous silica sublayer contained uniform, ordered (P6 mm) mesopores of ca. 7.5 nm from mesoporous silica as well as macropores ( approximately mum) from interparticle voids, as evidenced by transmission electron microscopy and scanning electron microscopy analyses. The morphologies of the supported mesoporous silica could be manipulated, thus permitting the generation of uniform needlelike forms or uniform spheroid particles by varying the concentration of PSS-.

  8. Facile synthesis of phosphorus doped graphitic carbon nitride polymers with enhanced visible-light photocatalytic activity

    International Nuclear Information System (INIS)

    Zhang, Ligang; Chen, Xiufang; Guan, Jing; Jiang, Yijun; Hou, Tonggang; Mu, Xindong

    2013-01-01

    Graphical abstract: - Highlights: • P-doped g-C 3 N 4 has been prepared by a one-pot green synthetic approach. • The incorporation of P resulted in favorable textural and electronic properties. • Doping with P enhanced the visible-light photocatalytic activity of g-C 3 N 4 . • A postannealing treatment further enhanced the activity of P-doped g-C 3 N 4 . • Photogenerated holes were the main species responsible for the activity. - Abstract: Phosphorus-doped carbon nitride materials were prepared by a one-pot green synthetic approach using dicyandiamide monomer and a phosphorus containing ionic liquid as precursors. The as-prepared materials were subjected to several characterizations and investigated as metal-free photocatalysts for the degradation of organic pollutants (dyes like Rhodamine B, Methyl orange) in aqueous solution under visible light. Results revealed that phosphorus-doped carbon nitride have a higher photocatalytic activity for decomposing Rhodamine B and Methyl orange in aqueous solution than undoped g-C 3 N 4 , which was attributed to the favorable textural, optical and electronic properties caused by doping with phosphorus heteroatoms into carbon nitride host. A facile postannealing treatment further improved the activity of the photocatalytic system, due to the higher surface area and smaller structural size in the postcalcined catalysts. The phosphorus-doped carbon nitride showed high visible-light photocatalytic activity, making them promising materials for a wide range of potential applications in photochemistry

  9. Facile synthesis of Bi/BiOCl composite with selective photocatalytic properties

    International Nuclear Information System (INIS)

    Chen, Dongling; Zhang, Min; Lu, Qiuju; Chen, Junfang; Liu, Bitao; Wang, Zhaofeng

    2015-01-01

    This paper presents a novel and facile method to fabricate Bi/BiOCl composites with dominant (001) facets in situ via a microwave reduction route. Different characterization techniques, including X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), transmission scanning electron microscopy (TEM), UV–vis diffuse reflectance spectrometry (DRS), X-ray photoelectron spectroscopy (XPS), electron spin resonance spectroscopy (ESR), cathodoluminescence spectrum (CL), and lifetime, have been employed to investigate the structure, optical and electrical properties of the Bi/BiOCl composites. The experimental results show that the introduction of Bi particles can efficiently enhance the photocatalytic performance of BiOCl for the degradation of several dyes under ultraviolet (UV) light irradiation, especially for negative charged methyl orange (MO). Unlike the UV photocatalytic performance, such Bi/BiOCl composite shows higher degradation efficiency towards rhodamine B (RhB) than MO and methylene blue (MB) under visible light irradiation. This special photocatalytic performance can be ascribed to the synergistic effect between oxygen vacancies and Bi particles. This work provides new insights about the photodegradation mechanisms of MO, MB and RhB under UV and visible light irradiation, which would be helpful to guide the selection of an appropriate catalyst for other pollutants. - Highlights: • Bi/BiOCl composites were synthesized via a microwave reduction. • Tunable selectivity photocatalytic activity can be achieved. • Photodegradation mechanism under UV and visible light were proposed

  10. Facile solvothermal synthesis of a graphene nanosheet-bismuth oxide composite and its electrochemical characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Wang Huanwen [Key Laboratory of Eco-Environment-Related Polymer Materials of Ministry of Education, Key Laboratory of Polymer Materials of Gansu Province, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070 (China); Hu Zhongai, E-mail: zhongai@nwnu.edu.c [Key Laboratory of Eco-Environment-Related Polymer Materials of Ministry of Education, Key Laboratory of Polymer Materials of Gansu Province, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070 (China); Chang Yanqin; Chen Yanli; Lei Ziqiang; Zhang Ziyu; Yang Yuying [Key Laboratory of Eco-Environment-Related Polymer Materials of Ministry of Education, Key Laboratory of Polymer Materials of Gansu Province, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070 (China)

    2010-12-01

    This work demonstrates a novel and facile route for preparing graphene-based composites comprising of metal oxide nanoparticles and graphene. A graphene nanosheet-bismuth oxide composite as electrode materials of supercapacitors was firstly synthesized by thermally treating the graphene-bismuth composite, which was obtained through simultaneous solvothermal reduction of the colloidal dispersions of negatively charged graphene oxide sheets in N,N-dimethyl formamide (DMF) solution of bismuth cations at 180 {sup o}C. The morphology, composition, and microstructure of the composites together with pure graphite oxide, and graphene were characterized using powder X-ray diffraction (XRD), FT-IR, field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), thermogravimetry and differential thermogravimetry (TG-DTG). The electrochemical behaviors were measured by cyclic voltammogram (CV), galvanostatic charge-discharge and electrochemical impedance spectroscopy (EIS). The specific capacitance of 255 F g{sup -1} (based on composite) is obtained at a specific current of 1 A g{sup -1} as compared with 71 F g{sup -1} for pure graphene. The loaded-bismuth oxide achieves a specific capacitance as high as 757 F g{sup -1} even at 10 A g{sup -1}. In addition, the graphene nanosheet-bismuth oxide composite electrode exhibits the excellent rate capability and well reversibility.

  11. Facile synthesis of cobalt hexacyanoferrate/graphene nanocomposites for high-performance supercapacitor

    International Nuclear Information System (INIS)

    Wang, Jian-Gan; Zhang, Zhiyong; Liu, Xingrui; Wei, Bingqing

    2017-01-01

    Prussian blue and its analogues are promising for energy storage devices owing to the rigid open framework, yet suffer from poor conductivity and relatively low energy density. Herein, we report a facile preparation of cobalt hexacyanoferrate/reduced graphene oxide nanocomposites (CoHCF/rGO) for supercapacitors with enhanced performance. The CoHCF nanoparticles with a size of around 50 nm are adhered onto the rGO nanosheets, which, in turn, not only prevent the agglomeration of the CoHCF nanoparticles but also provide conductive network for fast electron transport. The CoHCF/rGO nanocomposite delivers a maximum specific capacitance of 361 F g"−"1 in Na_2SO_4 aqueous electrolyte. Asymmetric supercapacitor cells are assembled by pairing up an optimized nanocomposite electrode with an activated carbon negative electrode, which exhibits a wide reversible operating voltage of 2.0 V and a high energy density of 39.6 Wh kg"−"1. The enhanced electrochemical performance of CoHCF/rGO benefits from the strong synergistic utilization of CoHCF nanoparticles and rGO nanosheets, rendering the nanocomposites a great promise for high-performance supercapacitors.

  12. Facile synthesis of hierarchical nanostructured rutile titania for lithium-ion battery

    International Nuclear Information System (INIS)

    Fei Hailong; Wei Mingdeng

    2011-01-01

    Highlights: → Rutile TiO 2 sub-microflowers and sub-microspheres with different building blocks as anode materials of lithium-ion battery. → Controllable morphologies with oxalic acid by the hydrothermal technique. → Sub-microflower and sub-microspheres constructed by well organized nanorods exhibited high capacity and good cycle stability. → Small size building blocks nanorods enhance the transfer rate of Li-ion. - Abstract: A facile hydrothermal method is developed to prepare rutile titania sub-microflowers consisting of nanorods with oxalic acid and TiOSO 4 as reagents. The diameter of sub-microflowers and nanorods is found to be ca. 800 and 40 nm, respectively. Also, the shape and size of building blocks in rutile titania sub-microflowers can be considerably controlled via adjusting the reaction time and reactant amounts. Rutile titania sub-microflowers composed of nanorods display higher discharge capacity and better rate cycle stability than other rutile titania nanostructures as lithium-ion battery anode material due to enhancing the Li-ion transfer rate for small size building blocks.

  13. Facile solvothermal synthesis of a graphene nanosheet-bismuth oxide composite and its electrochemical characteristics

    International Nuclear Information System (INIS)

    Wang Huanwen; Hu Zhongai; Chang Yanqin; Chen Yanli; Lei Ziqiang; Zhang Ziyu; Yang Yuying

    2010-01-01

    This work demonstrates a novel and facile route for preparing graphene-based composites comprising of metal oxide nanoparticles and graphene. A graphene nanosheet-bismuth oxide composite as electrode materials of supercapacitors was firstly synthesized by thermally treating the graphene-bismuth composite, which was obtained through simultaneous solvothermal reduction of the colloidal dispersions of negatively charged graphene oxide sheets in N,N-dimethyl formamide (DMF) solution of bismuth cations at 180 o C. The morphology, composition, and microstructure of the composites together with pure graphite oxide, and graphene were characterized using powder X-ray diffraction (XRD), FT-IR, field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), thermogravimetry and differential thermogravimetry (TG-DTG). The electrochemical behaviors were measured by cyclic voltammogram (CV), galvanostatic charge-discharge and electrochemical impedance spectroscopy (EIS). The specific capacitance of 255 F g -1 (based on composite) is obtained at a specific current of 1 A g -1 as compared with 71 F g -1 for pure graphene. The loaded-bismuth oxide achieves a specific capacitance as high as 757 F g -1 even at 10 A g -1 . In addition, the graphene nanosheet-bismuth oxide composite electrode exhibits the excellent rate capability and well reversibility.

  14. Facile Synthesis of Calcium Borate Nanoparticles and the Annealing Effect on Their Structure and Size

    Directory of Open Access Journals (Sweden)

    Manizheh Navasery

    2012-11-01

    Full Text Available Calcium borate nanoparticles have been synthesized by a thermal treatment method via facile co-precipitation. Differences of annealing temperature and annealing time and their effects on crystal structure, particle size, size distribution and thermal stability of nanoparticles were investigated. The formation of calcium borate compound was characterized by X-ray diffraction (XRD and Fourier Transform Infrared spectroscopy (FTIR, Transmission electron microscopy (TEM, and Thermogravimetry (TGA. The XRD patterns revealed that the co-precipitated samples annealed at 700 °C for 3 h annealing time formed an amorphous structure and the transformation into a crystalline structure only occurred after 5 h annealing time. It was found that the samples annealed at 900 °C are mostly metaborate (CaB2O4 nanoparticles and tetraborate (CaB4O7 nanoparticles only observed at 970 °C, which was confirmed by FTIR. The TEM images indicated that with increasing the annealing time and temperature, the average particle size increases. TGA analysis confirmed the thermal stability of the annealed samples at higher temperatures.

  15. Facile synthesis and enhanced visible-light photocatalysis of graphitic carbon nitride composite semiconductors.

    Science.gov (United States)

    Li, Huiquan; Liu, Yuxing; Gao, Xing; Fu, Cong; Wang, Xinchen

    2015-04-13

    The semiconductor heterojunction has been an effective architecture to enhance photocatalytic activity by promoting photogenerated charge separation. Here, graphitic carbon nitride (CN) and B-modified graphitic carbon nitride (CNB) composite semiconductors were fabricated by a facile calcination process using cheap, sustainable, and easily available sodium tetraphenylboron and urea as precursors. The synthetic CN-CNB-25 semiconductor with a suitable CNB content showed the highest visible-light activity. Its degradation ratio for methyl orange and phenol was more than twice that of CN and CNB and its H2 evolution rate was ∼3.4 and ∼1.8 times higher than that of CN and CNB, respectively. It also displayed excellent stability and reusability. The enhanced activity of CN-CNB-25 was attributed predominantly to the efficient separation of photoinduced electrons and holes. This paper describes a visible-light-responsive CN composite semiconductor with great potential in environmental and energy applications. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Facile synthesis of high strength hot-water wood extract films with oxygen-barrier performance

    Science.gov (United States)

    Chen, Ge-Gu; Fu, Gen-Que; Wang, Xiao-Jun; Gong, Xiao-Dong; Niu, Ya-Shuai; Peng, Feng; Yao, Chun-Li; Sun, Run-Cang

    2017-01-01

    Biobased nanocomposite films for food packaging with high mechanical strength and good oxygen-barrier performance were developed using a hot-water wood extract (HWE). In this work, a facile approach to produce HWE/montmorillonite (MMT) based nanocomposite films with excellent physical properties is described. The focus of this study was to determine the effects of the MMT content on the structure and mechanical properties of nanocomposites and the effects of carboxymethyl cellulose (CMC) on the physical properties of the HWE-MMT films. The experimental results suggested that the intercalation of HWE and CMC in montmorillonite could produce compact, robust films with a nacre-like structure and multifunctional characteristics. This results of this study showed that the mechanical properties of the film designated FCMC0.05 (91.5 MPa) were dramatically enhanced because the proportion of HWE, MMT and CMC was 1:1.5:0.05. In addition, the optimized films exhibited an oxygen permeability below 2.0 cm3 μm/day·m2·kPa, as well as good thermal stability due to the small amount of CMC. These results provide a comprehensive understanding for further development of high-performance nanocomposites which are based on natural polymers (HWE) and assembled layered clays (MMT). These films offer great potential in the field of sustainable packaging.

  17. Facile Synthesis and Optical Properties of Small Selenium Nanocrystals and Nanorods

    Science.gov (United States)

    Jiang, Fengrui; Cai, Weiquan; Tan, Guolong

    2017-06-01

    Selenium is an important element for human's health, small size is very helpful for Se nanoparticles to be absorbed by human's body. Here, we present a facile approach to fabrication of small selenium nanoparticles (Nano-Se) as well as nanorods by dissolving sodium selenite (Na2SeO3) in glycerin and using glucose as the reduction agent. The as-prepared selenium nanoparticles have been characterized by X-ray diffraction (XRD), UV-Vis absorption spectroscopy and high resolution transmission electron microscope (HRTEM). The morphology of small Se nanoparticles and nanorods have been demonstrated in the TEM images. A small amount of 3-mercaptoproprionic acid (MPA) and glycerin play a key role on controlling the particle size and stabilize the dispersion of Nano-Se in the glycerin solution. In this way, we obtained very small and uniform Se nanoparticles; whose size ranges from 2 to 6 nm. This dimension is much smaller than the best value (>20 nm) ever reported in the literatures. Strong quantum confinement effect has been observed upon the size-dependent optical spectrum of these Se nanoparticles.

  18. Facile Synthesis of Gd-Functionalized Gold Nanoclusters as Potential MRI/CT Contrast Agents

    Directory of Open Access Journals (Sweden)

    Wenjun Le

    2016-04-01

    Full Text Available Multi-modal imaging plays a key role in the earlier detection of disease. In this work, a facile bioinspired method was developed to synthesize Gd-functionalized gold nanoclusters (Gd-Au NCs. The Gd-Au NCs exhibit a uniform size, with an average size of 5.6 nm in dynamic light scattering (DLS, which is a bit bigger than gold clusters (3.74 nm, DLS, while the fluorescent properties of Gd-Au NCs are almost the same as that of Au NCs. Moreover, the Gd-Au NCs exhibit a high longitudinal relaxivity value (r1 of 22.111 s−1 per mM of Gd in phosphate-buffered saline (PBS, which is six times higher than that of commercial Magnevist (A complex of gadolinium with a chelating agent, diethylenetriamine penta-acetic acid, Gd-DTPA, r1 = 3.56 mM−1·s−1. Besides, as evaluated by nano single photon emission computed tomography (SPECT and computed tomography (CT the Gd-Au NCs have a potential application as CT contrast agents because of the Au element. Finally, the Gd-Au NCs show little cytotoxicity, even when the Au concentration is up to 250 μM. Thus, the Gd-Au NCs can act as multi-modal imaging contrast agents.

  19. Tubular combustion

    CERN Document Server

    Ishizuka, Satoru

    2014-01-01

    Tubular combustors are cylindrical tubes where flame ignition and propagation occur in a spatially confined, highly controlled environment, in a nearly flat, elongated geometry. This allows for some unique advantages where extremely even heat dispersion is required over a large surface while still maintaining fuel efficiency. Tubular combustors also allow for easy flexibility in type of fuel source, allowing for quick changeover to meet various needs and changing fuel pricing. This new addition to the MP sustainable energy series will provide the most up-to-date research on tubular combustion--some of it only now coming out of private proprietary protection. Plentiful examples of current applications along with a good explanation of background theory will offer readers an invaluable guide on this promising energy technology. Highlights include: * An introduction to the theory of tubular flames * The "how to" of maintaining stability of tubular flames through continuous combustion * Examples of both small-scal...

  20. Facile Synthesis of Monodispersed Polysulfide Spheres for Building Structural Colors with High Color Visibility and Broad Viewing Angle.

    Science.gov (United States)

    Li, Feihu; Tang, Bingtao; Wu, Suli; Zhang, Shufen

    2017-01-01

    The synthesis and assembly of monodispersed colloidal spheres are currently the subject of extensive investigation to fabricate artificial structural color materials. However, artificial structural colors from general colloidal crystals still suffer from the low color visibility and strong viewing angle dependence which seriously hinder their practical application in paints, colorimetric sensors, and color displays. Herein, monodispersed polysulfide (PSF) spheres with intrinsic high refractive index (as high as 1.858) and light-absorbing characteristics are designed, synthesized through a facile polycondensation and crosslinking process between sodium disulfide and 1,2,3-trichloropropane. Owing to their high monodispersity, sufficient surface charge, and good dispersion stability, the PSF spheres can be assembled into large-scale and high-quality 3D photonic crystals. More importantly, high structural color visibility and broad viewing angle are easily achieved because the unique features of PSF can remarkably enhance the relative reflectivity and eliminate the disturbance of scattering and background light. The results of this study provide a simple and efficient strategy to create structural colors with high color visibility, which is very important for their practical application. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.