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Sample records for nano-sized zn powder

  1. Oxidation of nano-sized aluminum powders

    International Nuclear Information System (INIS)

    Vorozhtsov, A.B.; Lerner, M.; Rodkevich, N.; Nie, H.; Abraham, A.; Schoenitz, M.; Dreizin, E.L.

    2016-01-01

    Highlights: • Weight gain measured in TG oxidation experiments was split between particles of different sizes. • Reaction kinetics obtained by isoconversion explicitly accounting for the effect of size distribution. • Activation energy is obtained as a function of oxide thickness for growth of amorphous alumina. • Oxidation mechanism for nanopowders remains the same as for coarser aluminum powders. - Abstract: Oxidation of aluminum nanopowders obtained by electro-exploded wires is studied. Particle size distributions are obtained from transmission electron microscopy (TEM) images. Thermo-gravimetric (TG) experiments are complemented by TEM and XRD studies of partially oxidized particles. Qualitatively, oxidation follows the mechanism developed for coarser aluminum powder and resulting in formation of hollow oxide shells. Sintering of particles is also observed. The TG results are processed to account explicitly for the particle size distribution and spherical shapes, so that oxidation of particles of different sizes is characterized. The apparent activation energy is obtained as a function of the reaction progress using model-free isoconversion processing of experimental data. A complete phenomenological oxidation model is then proposed assuming a spherically symmetric geometry. The oxidation kinetics of aluminum powder is shown to be unaffected by particle sizes reduced down to tens of nm. The apparent activation energy describing growth of amorphous alumina is increasing at the very early stages of oxidation. The higher activation energy is likely associated with an increasing homogeneity in the growing amorphous oxide layer, initially containing multiple defects and imperfections. The trends describing changes in both activation energy and pre-exponent of the growing amorphous oxide are useful for predicting ignition delays of aluminum particles. The kinetic trends describing activation energies and pre-exponents in a broader range of the oxide

  2. Microwave sintering of nano size powder β-TCP bioceramics

    Directory of Open Access Journals (Sweden)

    Mirhadi B.

    2014-01-01

    Full Text Available A nano sized beta tricalcium phosphate (β-TCP powder was conventional sintered (CS and microwave sintered (MW, in order to obtain dense β-TCP ceramics. In this work the effect of microwave sintering conditions on the microstructure, phase composition and mechanical properties of materials based on tricalcium phosphate (TCP was investigated by SEM (scanning electron microscopyand XRD(X-ray diffraction and then compared with conventional sintered samples. Nano-size β-TCP powders with average grain size of 80 nm were prepared by the wet chemical precipitation method with calcium nitrate and diammonium hydrogen phosphate as calcium and phosphorus precursors, respectively. The precipitation process employed was also found to be suitable for the production of submicrometre β-TCP powder in situ. The β-TCP samples microwave (MW sintered for 15 min at 1100°C, with average grain size of 3μm, showed better densification, higher density and certainly higher hardness than samples conventionally sintered for 2 h at the same temperature. By comparing sintered and MW sintered β-TCP samples, it was concluded that MW sintered β-TCP samples have superior mechanical properties.

  3. Luminescence properties of YAG:Nd nano-sized ceramic powders ...

    Indian Academy of Sciences (India)

    Abstract. Nano-sized ceramic powders with weaker aggregation of Nd3+-doped yttrium aluminum garnet. (YAG:Nd3+) were synthesized via co-microemulsion and microwave heating. This method provides a limited small space in a micelle for the formation of nano-sized precursors. It also requires a very short heating time, ...

  4. Magnetic properties of Sn-substituted Ni-Zn ferrites synthesized from nano-sized powders of NiO, ZnO, Fe2O3, and SnO2

    Science.gov (United States)

    Ali, MA; Uddin, MM; Khan, MNI; Chowdhury, FUZ; Hoque, SM; Liba, SI

    2017-06-01

    A series of Ni0.6-x/2Zn0.4-x/2Sn x Fe2O4 (x = 0.0, 0.05, 0.1, 0.15, 0.2, and 0.3) (NZSFO) ferrite composities have been synthesized from nano powders using a standard solid state reaction technique. The spinel cubic structure of the investigated samples has been confirmed by x-ray diffraction (XRD). The magnetic properties such as saturation magnetization ({M}{{s}}), remanent magnetization ({M}{{r}}), coercive field ({H}{{c}}), and Bohr magneton (μ) are calculated from the hysteresis loops. The value of {M}{{s}} is found to decrease with increasing Sn content in the samples. This change is successfully explained by the variation of A-B interaction strength due to Sn substitution in different sites. The compositional stability and quality of the prepared ferrite composites have also been endorsed by the fairly constant initial permeability ({μ }^{\\prime }) over a wide range of frequency. The decreasing trend of {μ }^{\\prime } with increasing Sn content has been observed. Curie temperature {T}{{C}} has been found to increase with the increase in Sn content. A wide spread frequency utility zone indicates that the NZSFO can be considered as a good candidate for use in broadband pulse transformers and wide band read-write heads for video recording. The composition of x = 0.05 shows unusual results and the possible reason is also mentioned with the established formalism.

  5. The Nano-Sized In2O3 Powder Synthesis by Sol-Gel Method

    Institute of Scientific and Technical Information of China (English)

    潘庆谊; 程知萱; 等

    2002-01-01

    Wiwh InCl3·4H2O being used as raw materials,the precursor of nano-sized In2O3 powder was prepared by hydrolysis,peptization and gelation of InCl3·4H2O.After calcination,nano-sized In2O3 powder was obtained.The powder was characterized by thermogravimetric and differential thermal analysis(TG-DTA).X-ray diffractometry(XRD)and transmission electron microscopy(TEM),respectively,Calculation revealed that the mean crystablline size increased with increasing the calcination temperature,but crystal lattice distortion rate decreased with the increasing in the average crystalline size.This indicated that the smaller the particle size,the bigger the crystal lattice distortion,the worse the crystal growing.The activation energies for growth of nano-sized In2O3 were calculated to be 4.75kJ·mol-1 at the calcination temperature up tp 500℃ and 66.40kJ· mol-1 at the calcination temperature over 600℃.TEM photos revealed that the addition of the chemical additive(OP-10)greatly influenced the morphology and size of In2O3 particles.

  6. Plasma-arc reactor for production possibility of powdered nano-size materials

    International Nuclear Information System (INIS)

    Hadzhiyski, V; Mihovsky, M; Gavrilova, R

    2011-01-01

    Nano-size materials of various chemical compositions find increasing application in life nowadays due to some of their unique properties. Plasma technologies are widely used in the production of a range of powdered nano-size materials (metals, alloys, oxides, nitrides, carbides, borides, carbonitrides, etc.), that have relatively high melting temperatures. Until recently, the so-called RF-plasma generated in induction plasma torches was most frequently applied. The subject of this paper is the developments of a new type of plasma-arc reactor, operated with transferred arc system for production of disperse nano-size materials. The new characteristics of the PLASMALAB reactor are the method of feeding the charge, plasma arc control and anode design. The disperse charge is fed by a charge feeding system operating on gravity principle through a hollow cathode of an arc plasma torch situated along the axis of a water-cooled wall vertical tubular reactor. The powdered material is brought into the zone of a plasma space generated by the DC rotating transferred plasma arc. The arc is subjected to Auto-Electro-Magnetic Rotation (AEMR) by an inductor serially connected to the anode circuit. The anode is in the form of a water-cooled copper ring. It is mounted concentrically within the cylindrical reactor, with its lower part electrically insulated from it. The electric parameters of the arc in the reactor and the quantity of processed charge are maintained at a level permitting generation of a volumetric plasma discharge. This mode enables one to attain high mean mass temperature while the processed disperse material flows along the reactor axis through the plasma zone where the main physico-chemical processes take place. The product obtained leaves the reactor through the annular anode, from where it enters a cooling chamber for fixing the produced nano-structure. Experiments for AlN synthesis from aluminium power and nitrogen were carried out using the plasma reactor

  7. Preparation of soft-agglomerated nano-sized ceramic powders by sol-gel combustion process

    International Nuclear Information System (INIS)

    Feng, Q.; Ma, X.H.; Yan, Q.Z.; Ge, C.C.

    2009-01-01

    The soft-agglomerated Gd 2 BaCuO 5 (Gd211) nano-powders were synthesized by sol-gel combustion process with binary ligand and the special pretreatment on gel. The mechanism of the formation of weakly agglomerated structure was studied in detail. The results showed that network structure in gelation process was found to be a decisive factor for preventing agglomeration of colloidal particles. The removal of free water, coordinated water, and most of hydroxyl groups during pretreatment further inhibited the formation of hydrogen bonds between adjacent particles. The soft-agglomeration of the particles was confirmed by isolated particles in calcined Gd211 powders and in green compact, a narrow monomodal pore size distribution of the green compact and the low agglomeration coefficient of the calcined Gd211 powder. Extension this process to synthesis of BaCeO 3 , BaTiO 3 and Ce 0.8 Sm 0.2 O 1.9 powders, also led to weakly agglomerated nano-powders. It suggests that this method represents a powerful and facile method for the creation of doped and multi-component nano-sized ceramic powders.

  8. Synthesis of nano-sized amorphous boron powders through active dilution self-propagating high-temperature synthesis method

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jilin [The State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Gu, Yunle [School of Material Science and Engineering, Wuhan Institute of Technology, Wuhan 430073 (China); Li, Zili [The State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Wang, Weimin, E-mail: wangwm@hotmail.com [The State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Fu, Zhengyi [The State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China)

    2013-06-01

    Graphical abstract: Nano-sized amorphous boron powders were synthesized by active dilution self-propagating high-temperature synthesis (SHS) method. The effects of endothermic reaction rate, the possible chemical reaction mechanism and active dilution model for synthesis of the product were also discussed. Highlights: ► Nano-sized amorphous boron powders were synthesized by active dilution self-propagating high-temperature synthesis method. ► The morphology, particle size and purity of the samples could be effectively controlled via changing the endothermic rate. ► The diluter KBH{sub 4} played an important role in active dilution synthesis of amorphous nano-sized boron powders. ► The active dilution method could be further popularized and become a common approach to prepare various inorganic materials. - Abstract: Nano-sized amorphous boron powders were synthesized by active dilution self-propagating high-temperature synthesis (SHS) method at temperatures ranging from 700 °C to 850 °C in a SHS furnace using Mg, B{sub 2}O{sub 3} and KBH{sub 4} as raw materials. Samples were characterized by X-ray powder diffraction (XRD), Laser particle size analyzer, Fourier transform infrared spectra (FTIR), X-ray energy dispersive spectroscopy (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and high-resolution transmission TEM (HRTEM). The boron powders demonstrated an average particle size of 50 nm with a purity of 95.64 wt.%. The diluter KBH{sub 4} played an important role in the active dilution synthesis of amorphous nano-sized boron powders. The effects of endothermic reaction rate, the possible chemical reaction mechanism and active dilution model for synthesis of the product were also discussed.

  9. Synthesis of nano-sized amorphous boron powders through active dilution self-propagating high-temperature synthesis method

    International Nuclear Information System (INIS)

    Wang, Jilin; Gu, Yunle; Li, Zili; Wang, Weimin; Fu, Zhengyi

    2013-01-01

    Graphical abstract: Nano-sized amorphous boron powders were synthesized by active dilution self-propagating high-temperature synthesis (SHS) method. The effects of endothermic reaction rate, the possible chemical reaction mechanism and active dilution model for synthesis of the product were also discussed. Highlights: ► Nano-sized amorphous boron powders were synthesized by active dilution self-propagating high-temperature synthesis method. ► The morphology, particle size and purity of the samples could be effectively controlled via changing the endothermic rate. ► The diluter KBH 4 played an important role in active dilution synthesis of amorphous nano-sized boron powders. ► The active dilution method could be further popularized and become a common approach to prepare various inorganic materials. - Abstract: Nano-sized amorphous boron powders were synthesized by active dilution self-propagating high-temperature synthesis (SHS) method at temperatures ranging from 700 °C to 850 °C in a SHS furnace using Mg, B 2 O 3 and KBH 4 as raw materials. Samples were characterized by X-ray powder diffraction (XRD), Laser particle size analyzer, Fourier transform infrared spectra (FTIR), X-ray energy dispersive spectroscopy (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and high-resolution transmission TEM (HRTEM). The boron powders demonstrated an average particle size of 50 nm with a purity of 95.64 wt.%. The diluter KBH 4 played an important role in the active dilution synthesis of amorphous nano-sized boron powders. The effects of endothermic reaction rate, the possible chemical reaction mechanism and active dilution model for synthesis of the product were also discussed

  10. 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.

  11. Influence of Nano sized Silicon Oxide on the Luminescent Properties of Zn O Nanoparticles

    International Nuclear Information System (INIS)

    Shvalagin, V.; Grodziuk, G.; Kurmach, M.; Granchak, V.; Sarapulova, O.; Sherstiuk, V.

    2016-01-01

    For practical use of nano sized zinc oxide as the phosphor its luminescence quantum yields should be maximized. The aim of this work was to enhance luminescent properties of Zn O nanoparticles and obtain high-luminescent Zn O/SiO 2 composites using simpler approaches to colloidal synthesis. The luminescence intensity of zinc oxide nanoparticles was increased about 3 times by addition of silica nano crystals to the source solutions during the synthesis of Zn O nanoparticles. Then the quantum yield of luminescence of the obtained Zn O/SiO 2 composites is more than 30%. Such an impact of silica is suggested to be caused by the distribution of Zn O nano crystals on the surface of silica, which reduces the probability of separation of photo generated charges between the zinc oxide nanoparticles of different sizes, and as a consequence, there is a significant increase of the luminescence intensity of Zn O nanoparticles. This way of increasing nano-Zn O luminescence intensity facilitates its use in a variety of devices, including optical ultraviolet and visible screens, luminescent markers, antibacterial coatings, luminescent solar concentrators, luminescent inks for security printing, and food packaging with abilities of informing consumers about the quality and safety of the packaged product.

  12. Direct synthesis of nano-sized glass powders with spherical shape by RF (radio frequency) thermal plasma

    International Nuclear Information System (INIS)

    Seo, J.H.; Kim, J.S.; Lee, M.Y.; Ju, W.T.; Nam, I.T.

    2011-01-01

    A new route for obtaining very small, spheroid glass powders is demonstrated using an RF (radio frequency) thermal plasma system. During the process, four kinds of chemicals, here SiO 2 , B 2 O 3 , BaCO 3 , and K 2 CO 3 , were mixed at pre-set weight ratios, spray-dried, calcined at 250 deg. C for 3 h, and crushed into fragments. Then, they were successfully reformed into nano-sized amorphous powders (< 200 nm) with spherical shape by injecting them along the centerline of an RF thermal plasma reactor at ∼ 24 kW. The as-synthesized powders show negligible (< 1%) composition changes when compared with the injected precursors of raw material compounds.

  13. Spectroscopic investigation on assisted sonocatalytic damage of bovine serum albumin (BSA) by metronidazole (MTZ) under ultrasonic irradiation combined with nano-sized ZnO

    Science.gov (United States)

    Gao, Jingqun; Liu, Bin; Wang, Jun; Jin, Xudong; Jiang, Renzheng; Liu, Lijun; Wang, Baoxin; Xu, Yongnan

    2010-11-01

    The previous work proved that the bovine serum albumin (BSA) could be damaged under the combined action of ultrasonic irradiation and ZnO. In this work, the assisted sonocatalytic damage of BSA using metronidazole (MTZ) as a sensitizer was further investigated by means of UV-vis and fluorescence spectra. The results indicated that the adding of MTZ could obviously promote the sonocatalytic damage of BSA under ultrasonic irradiation in the presence of nano-sized ZnO powder. Furthermore, it was found that the damage degree of BSA was aggravated by some influencing factors except ionic kind and strength. In addition, the damage site of BSA was also studied with synchronous fluorescence technology. It was found that the damage site was mainly at tryptophan (Trp) residue.

  14. Radical change of Zn speciation in pig slurry amended soil: Key role of nano-sized sulfide particles.

    Science.gov (United States)

    Formentini, Thiago Augusto; Legros, Samuel; Fernandes, Cristovão Vicente Scapulatempo; Pinheiro, Adilson; Le Bars, Maureen; Levard, Clément; Mallmann, Fábio Joel Kochem; da Veiga, Milton; Doelsch, Emmanuel

    2017-03-01

    Spreading livestock manure as fertilizer on farmlands is a widespread practice. It represents the major source of heavy metal(loid)s (HM) input in agricultural soils. Since zinc (Zn) is present at high concentrations in manure, it poses special environmental concerns related to phytotoxicity, groundwater contamination, and introduction in the food chain. Therefore, investigations on the fate and behavior of manure-borne Zn, when it enters the soil environment, are necessary to predict the environmental effects. Nevertheless, long-term field studies assessing Zn speciation in the organic waste matrix, as well as within the soil after manure application, are lacking. This study was designed to fill this gap. Using SEM-EDS and XAS analysis, we reported the following new results: (i) ZnS made up 100% of the Zn speciation in the pig slurry (the highest proportion of ZnS ever observed in organic waste); and (ii) ZnS aggregates were about 1-μm diameter (the smallest particle size ever reported in pig slurry). Moreover, the pig slurry containing ZnS was spread on the soil over an 11-year period, totaling 22 applications, and the resulting Zn speciation within the amended soil was analyzed. Surprisingly, ZnS, i.e. the only species responsible for a nearly 2-fold increase in the Zn concentration within the amended soil, was not detected in this soil. Based on SEM-EDS and XAS observations, we put forward the hypothesis that Zn in the pig slurry consisted of nano-sized ZnS crystallites that further aggregated. The low stability of ZnS nanoparticles within oxic and complex environments such as the studied soil was the key explanation for the radical change in pig slurry-borne Zn speciation after long-term amendments. Copyright © 2016 Elsevier Ltd. All rights reserved.

  15. Characteristics Of The Porous Body Sintered By Nano-Sized Fe-Cr-Al Alloy Powder

    Directory of Open Access Journals (Sweden)

    Lee Su-In

    2015-06-01

    Full Text Available Porous metal with uniform honeycomb structure was successfully produced by sintering using Fe-Cr-Al nano powder, which was prepared by the pulsed wire evaporation (PWE in ethanol. Its process consisted of the several steps; 1 coating on the surface of polyurethane sponge with the liquid droplets generated from the ethanol-based slurry where the Fe-Cr-Al nano powders were uniformly dispersed, 2 heat treatment of debinding to remove the polyurethane sponge and 3 sintering of the porous green body formed by Fe-Cr-Al nano powders. The strut thickness of porous Fe-Cr-Al was increased by the increase of spraying times in ESP step. Also, The shrinkages and the oxidation resistance of the sintered porous body was increased with increase of sintering temperature. The optimal sintering temperature was shown to 1450°C in views to maximize the oxidation resistance and sinterability.

  16. Investigation of effective parameters in preparation and controlling lithium fluoride nano size powder

    International Nuclear Information System (INIS)

    Naderi, S.; Sarraf Mamoory, F.; Riahi Noori, N.

    2007-01-01

    In this research, the reaction of LiOH + HF+LiF+H 2 O has been selected and some precipitation parameters such as pH, temperature, time, super saturation, q d agitation type have been studied, and controlled. The morphology, phase analysis and particle size of the resulting powders were analyzed by SEM, XRD and LPSA. Finally, at temperature 2S d ig C , pH of about 2-3, reaction time less than 1 sec, and agitation by ultrasonic bath, the pure nano lithium fluoride powders of about 100 nm were produced

  17. Hydrothermal synthesis and characterization of hydroxyapatite and fluorhydroxyapatite nano-size powders

    International Nuclear Information System (INIS)

    Montazeri, Leila; Javadpour, Jafar; Shokrgozar, Mohammad Ali; Bonakdar, Shahin; Javadian, Sayfoddin

    2010-01-01

    Pure hydroxyapatite (HAp) and fluoride-containing apatite powders (FHAp) were synthesized using a hydrothermal method. The powders were assessed by x-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscope (SEM) and F-selective electrode. X-ray diffraction results revealed the formation of single phase apatite structure for all the compositions synthesized in this work. However, the addition of a fluoride ion led to a systematic shift in the (3 0 0) peak of the XRD pattern as well as modifications in the FTIR spectra. It was found that the efficiency of fluoride ion incorporation decreased with the increase in the fluoride ion content. Fluorine incorporation efficiency was around 60% for most of the FHAp samples prepared in the current study. Smaller and less agglomerated particles were obtained by fluorine substitution. The bioactivity of the powder samples with different fluoride contents was compared by performing cell proliferation, alkaline phosphatase (ALP) and Alizarin red staining assays. Human osteoblast cells were used to assess the cellular responses to the powder samples in this study. Results demonstrated a strong dependence of different cell activities on the level of fluoridation.

  18. Structural and magnetic properties of nano-sized NiCuZn ferrites synthesized by co-precipitation method with ultrasound irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Harzali, Hassen, E-mail: harzali@mines-albi.fr [Laboratory of Applied Mineral Chemistry, Faculty of Sciences, University Tunis ElManar, Campus University, Farhat Hached El-Manar, 2092 Tunis (Tunisia); Saida, Fairouz; Marzouki, Arij; Megriche, Adel [Laboratory of Applied Mineral Chemistry, Faculty of Sciences, University Tunis ElManar, Campus University, Farhat Hached El-Manar, 2092 Tunis (Tunisia); Baillon, Fabien; Espitalier, Fabienne [Université de Toulouse, Mines Albi, CNRS, Centre RAPSODEE, Campus Jarlard, F-81013 Albi CT cedex 09 (France); Mgaidi, Arbi [Laboratory of Applied Mineral Chemistry, Faculty of Sciences, University Tunis ElManar, Campus University, Farhat Hached El-Manar, 2092 Tunis (Tunisia); Taibah University, Faculty of Sciences & art, Al Ula (Saudi Arabia)

    2016-12-01

    Sonochemically assisted co-precipitation has been used to prepare nano-sized Ni–Cu–Zn-ferrite powders. A suspension of constituent hydroxides was ultrasonically irradiated for various times at different temperatures with high intensity ultrasound radiation using a direct immersion titanium horn. Structural and magnetic properties were investigated using X-diffraction (XRD), FT-IR spectroscopy, transmission electron microscopy (TEM), Nitrogen adsorption at 77 K (BET) and Vibrating sample magnetometer (VSM). Preliminary experimental results relative to optimal parameters showed that reaction time t=2 h, temperature θ=90 °C and dissipated Power P{sub diss}=46.27 W. At these conditions, this work shows the formation of nanocrystalline single-phase structure with particle size 10–25 nm. Also, ours magnetic measurements proved that the sonochemistry method has a great influence on enhancing the magnetic properties of the ferrite. - Highlights: • Coprecipitation experiments were carried out with ultrasound. • The spinel ferrite NiCuZn was perfectly synthesized by ultrasound. • The saturation magnetization and crystals size are found to be correlated as the dissipated power was varied.

  19. Structural and magnetic properties of nano-sized NiCuZn ferrites synthesized by co-precipitation method with ultrasound irradiation

    International Nuclear Information System (INIS)

    Harzali, Hassen; Saida, Fairouz; Marzouki, Arij; Megriche, Adel; Baillon, Fabien; Espitalier, Fabienne; Mgaidi, Arbi

    2016-01-01

    Sonochemically assisted co-precipitation has been used to prepare nano-sized Ni–Cu–Zn-ferrite powders. A suspension of constituent hydroxides was ultrasonically irradiated for various times at different temperatures with high intensity ultrasound radiation using a direct immersion titanium horn. Structural and magnetic properties were investigated using X-diffraction (XRD), FT-IR spectroscopy, transmission electron microscopy (TEM), Nitrogen adsorption at 77 K (BET) and Vibrating sample magnetometer (VSM). Preliminary experimental results relative to optimal parameters showed that reaction time t=2 h, temperature θ=90 °C and dissipated Power P_d_i_s_s=46.27 W. At these conditions, this work shows the formation of nanocrystalline single-phase structure with particle size 10–25 nm. Also, ours magnetic measurements proved that the sonochemistry method has a great influence on enhancing the magnetic properties of the ferrite. - Highlights: • Coprecipitation experiments were carried out with ultrasound. • The spinel ferrite NiCuZn was perfectly synthesized by ultrasound. • The saturation magnetization and crystals size are found to be correlated as the dissipated power was varied.

  20. The use of nano-sized eggshell powder for calcium fortification of cow?s and buffalo?s milk yogurts.

    Science.gov (United States)

    El-Shibiny, Safinaze; El-Gawad, Mona Abd El-Kader Mohamed Abd; Assem, Fayza Mohamed; El-Sayed, Samah Mosbah

    2018-01-01

    Calcium is an essential element for the growth, activity, and maintenance of the human body. Eggshells are a waste product which has received growing interest as a cheap and effective source of dietary calcium. Yogurt is a food which can be fortified with functional additives, including calcium. The aim of this study was to produce yogurt with a high calcium content by fortification with nano-sized eggshell powder (nano-ESP). Nano-sized ESP was prepared from pre-boiled and dried eggshell, using a ball mill. Yogurt was prepared from cow’s milk supplemented with 3% skimmed milk powder, and from buffalo’s milk fortified with 0.1, 0.2 and 0.3% and 0.1, 0.3 and 0.5% nano-ESP respectively. Electron microscopic transmission showed that the powder consisted of nano-sized crystalline struc- tures (~10 nm). Laser scattering showed that particles followed a normal distribution pattern with z-average of 590.5 nm, and had negative zeta-potential of –9.33 ±4.2 mV. Results regarding changes in yogurt composi- tion, acid development, calcium distribution, biochemical changes, textural parameters and sensory attributes have been presented and discussed. The addition of up to 0.3% nano-ESP made cow and buffalo high-calcium yogurts with an acceptable composition and quality. High-calcium yogurt may offer better health benefits, such as combating osteoporosis.

  1. Nano-sized Fe-metal catalyst on ZnO-SiO2: (photo-assisted deposition and impregnation) Synthesis routes and nanostructure characterization

    International Nuclear Information System (INIS)

    Mohamed, R.M.; Al-Rayyani, M.A.; Baeissa, E.S.; Mkhalid, I.A.

    2011-01-01

    Highlights: → We prepared Fe/ZnO-SiO 2 by two methods. → We tested photocatalytic activity for degradation of methylene blue dye. → We controlled band gap and size. → We found activity of Fe/ZnO-SiO 2 prepared by PAD is hightest photocatalytic activity. - Abstract: A nano-sized Fe metal on ZnO-SiO 2 was synthesized using the photo-assisted deposition (PAD) and impregnation routes. The obtained samples were characterized by a series of techniques including X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy, N 2 adsorption, extended X-ray absorption fine structure (EXAFS), and transmission electron microscopy (TEM). Photocatalytic reactivity using Fe-ZnO-SiO 2 catalysts under visible-light condition on the degradation of methylene blue dye was evaluated. The results of characterization reveal, a notable photocatalytic activity of PAD:Fe-ZnO-SiO 2 which was about 9 and 12 times higher than that of Img:Fe-ZnO-SiO 2 and ZnO-SiO 2 , respectively.

  2. Nano structural Features of Silver Nanoparticles Powder Synthesized through Concurrent Formation of the Nano sized Particles of Both Starch and Silver

    International Nuclear Information System (INIS)

    Hebeish, A.; El-Rafie, M.H.; El-Sheikh, M.A.; El-Naggar, M.E.

    2013-01-01

    Green innovative strategy was developed to accomplish silver nanoparticles formation of starch-silver nanoparticles (St-AgNPs) in the powder form. Thus, St-AgNPs were synthesized through concurrent formation of the nano sized particles of both starch and silver. The alkali dissolved starch acts as reducing agent for silver ions and as stabilizing agent for the formed AgNPs. The chemical reduction process occurred in water bath under high-speed homogenizer. After completion of the reaction, the colloidal solution of AgNPs coated with alkali dissolved starch was cooled and precipitated using ethanol. The powder precipitate was collected by centrifugation, then washed, and dried; St-AgNPs powder was characterized using state-of-the-art facilities including UV-vis spectroscopy, Transmission Electron Microscopy (TEM), particle size analyzer (PS), Polydispersity index (PdI), Zeta potential (ZP), XRD, FT-IR, EDX, and TGA. TEM and XRD indicate that the average size of pure AgNPs does not exceed 20 nm with spherical shape and high concentration of AgNPs (30000 ppm). The results obtained from TGA indicates that the higher thermal stability of starch coated AgNPS than that of starch nanoparticles alone. In addition to the data obtained from EDX which reveals the presence of AgNPs and the data obtained from particle size analyzer and zeta potential determination indicate that the good uniformity and the highly stability of St-AgNPs).

  3. High heat generation ability in AC magnetic field for nano-sized magnetic Y3Fe5O12 powder prepared by bead milling

    International Nuclear Information System (INIS)

    Aono, Hiromichi; Ebara, Hiroki; Senba, Ryota; Naohara, Takashi; Maehara, Tsunehiro; Hirazawa, Hideyuki; Watanabe, Yuji

    2012-01-01

    Nano-sized magnetic Y 3 Fe 5 O 12 ferrite having a high heat generation ability in an AC magnetic field was prepared by bead milling. A commercial powder sample (non-milled sample) of ca. 2.9 μm in particle size did not show any temperature enhancement in the AC magnetic field. The heat generation ability in the AC magnetic field improved with a decrease in the average crystallite size for the bead-milled Y 3 Fe 5 O 12 ferrites. The highest heat ability in the AC magnetic field was for the fine Y 3 Fe 5 O 12 powder with a 15-nm crystallite size (the samples were milled for 4 h using 0.1 mmφ beads). The heat generation ability of the excessively milled Y 3 Fe 5 O 12 samples decreased. The main reason for the high heat generation property of the milled samples was ascribed to an increase in the Néel relaxation of the superparamagnetic material. The heat generation ability was not influenced by the concentration of the ferrite powder. For the samples milled for 4 h using 0.1 mmφ beads, the heat generation ability (W g −1 ) was estimated using a 3.58×10 −4 fH 2 frequency (f/kHz) and the magnetic field (H/kA m −1 ), which is the highest reported value of superparamagnetic materials. - Highlights: ► The nano-sized Y 3 Fe 5 O 12 powder prepared by bead-milling has the highest heat generation ability in an AC magnetic field. ► The heat generation properties are ascribed to an increase in the Néel relaxation of the superparamagnetic material. ► The heat ability (W g −1 ) can be estimated using 3.58×10 −4 fH 2 (f=kHz, H=kA m −1 ). ► This is an expectable material for use in a drug delivery system for the thermal coagulation therapy of cancer tumors.

  4. Spectrum designation and effect of Al substitution on the luminescence of Cr3+ doped ZnGa2O4 nano-sized phosphors

    International Nuclear Information System (INIS)

    Zhang Weiwei; Zhang Junying; Chen Ziyu; Wang Tianmin; Zheng Shukai

    2010-01-01

    Low-temperature photoluminescent spectra of ZnGa 2 O 4 :Cr 3+ nano-sized phosphors calcined at different temperatures were reported. The fine structure of the emission spectra has been designated to Cr 3+ ions in different sites including ideal octahedral, Zn-interstitial, Ga ZN 4 -Zn Ga 6 sites and Ga 2 O 3 impurity. The vibronic sidebands for both Stokes' and anti-Stokes' sides are related to the host lattice vibrations, which were confirmed by IR and Raman spectra. Al 3+ is substituted in Ga 3+ sites to form Zn(Ga 1-y Al y ) 2 O 4 :Cr 0.01 3+ (0≤y≤0.5). The blue shift and luminescent intensity variations of the charge transfer band and 3d-3d transitions in the spectra caused by Al substitution were related to larger band gap and stronger crystal field, respectively. The calculated crystal-field parameters indicated that Al incorporation enhanced the crystal field strength and induced more trigonal distortion due to different radii of Al 3+ and Ga 3+ .

  5. Effect of nano-sized cerium-zirconium oxide solid solution on far-infrared emission properties of tourmaline powders

    Science.gov (United States)

    Guo, Bin; Yang, Liqing; Hu, Weijie; Li, Wenlong; Wang, Haojing

    2015-10-01

    Far-infrared functional nanocomposites were prepared by the co-precipitation method using natural tourmaline (XY3Z6Si6O18(BO3)3V3W, where X is Na+, Ca2+, K+, or vacancy; Y is Mg2+, Fe2+, Mn2+, Al3+, Fe3+, Mn3+, Cr3+, Li+, or Ti4+; Z is Al3+, Mg2+, Cr3+, or V3+; V is O2-, OH-; and W is O2-, OH-, or F-) powders, ammonium cerium(IV) nitrate and zirconium(IV) nitrate pentahydrate as raw materials. The reference sample, tourmaline modified with ammonium cerium(IV) nitrate alone was also prepared by a similar precipitation route. The results of Fourier transform infrared spectroscopy show that tourmaline modified with Ce and Zr has a better far-infrared emission property than tourmaline modified with Ce alone. Through characterization by transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS), the mechanism for oxygen evolution during the heat process in the two composite materials was systematically studied. The XPS spectra show that Fe3+ ratio inside tourmaline modified with Ce alone can be raised by doping Zr. Moreover, it is showed that there is a higher Ce3+ ratio inside the tourmaline modified with Ce and Zr than tourmaline modified with Ce alone. In addition, XRD results indicate the formation of CeO2 and Ce1-xZrxO2 crystallites during the heat treatment and further TEM observations show they exist as nanoparticles on the surface of tourmaline powders. Based on these results, we attribute the improved far-infrared emission properties of Ce-Zr doped tourmaline to the enhanced unit cell shrinkage of the tourmaline arisen from much more oxidation of Fe2+ to Fe3+ inside the tourmaline caused by the change in the catalyst redox properties of CeO2 brought about by doping with Zr4+. In all samples, tourmaline modified with 7.14 wt.% Ce and 1.86 wt.% Zr calcined at 800∘C for 5 h has the best far-infrared emission property with the maximum emissivity value of 98%.

  6. Structural and optical characteristics of nano-sized structure of Zn0.5Cd0.5S thin films prepared by dip-coating method

    International Nuclear Information System (INIS)

    Rafea, M. Abdel; Farag, A.A.M.; Roushdy, N.

    2009-01-01

    In this work, a stoichiometry Zn 0.5 Cd 0.5 S nano-structured powder was synthesized. Thin films of different thicknesses of Zn 0.5 Cd 0.5 S were prepared by dip-coating method onto glass substrates. The X-ray diffraction analysis of the prepared powder and films were performed to investigate the crystalline structure. Some structural parameters such as the mean crystallite size and the internal lattice strain were calculated. The composition analysis was made by the energy dispersive X-ray technique, EDX. Scanning electron micrographs, SEM showed that the prepared films are nearly homogeneous and consists of nearly parallel surfaces and the thickness was determined by the cross section imaging. The transmission spectra, T(λ), of the films at normal incidence of light were obtained in the spectral region 190-1100 nm. The optical constants of Zn 0.5 Cd 0.5 S films were determined using the interference maxima and minima of the transmission spectrum. The dispersion of refractive index was discussed in terms of the single-oscillator model and the important oscillating parameters were determined. The dependence of absorption coefficient on the photon energy was determined and the analysis of the result showed that the optical transition in Zn 0.5 Cd 0.5 S is allowed and indirect. The thickness dependence of the obtained optical parameters was also considered.

  7. Thin film assembly of nano-sized Zn(II)-8-hydroxy-5,7-dinitroquinolate by using successive ion layer adsorption and reaction (SILAR) technique: characterization and optical-electrical-photovoltaic properties.

    Science.gov (United States)

    Farag, A A M; Haggag, Sawsan M S; Mahmoud, Mohamed E

    2012-07-01

    A method is described for thin film assembly of nano-sized Zn(II)-8-hydroxy-5,7-dinitroquinolate complex, Zn[((NO(2))(2)-8HQ)(2)] by using successive ion layer adsorption and reaction (SILAR) technique. Highly homogeneous assembled nano-sized metal complex thin films with particle size distribution in the range 27-47nm was identified by using scanning electron microscopy (SEM). Zn[((NO(2))(2)-8HQ)(2)] and [(NO(2))(2)-8HQ] ligand were studied by thermal gravimetric analysis (TGA). Graphical representation of temperature dependence of the dark electrical conductivity produced two distinct linear parts for two activation energies at 0.377eV and 1.11eV. The analysis of the spectral behavior of the absorption coefficient in the intrinsic absorption region reveals a direct allowed transition with a fundamental band gap of 2.74eV. The dark current density-voltage (J-V) characteristics showed the rectification effect due to the formation of junction barrier of Zn[((NO(2))(2)-8HQ)(2)] complex film/n-Si interface. The photocurrent in the reverse direction is strongly increased by photo-illumination and the photovoltaic characteristics were also determined and evaluated. Copyright © 2012 Elsevier B.V. All rights reserved.

  8. Structure and electromagnetic properties of NiZn spinel ferrite with nano-sized ZnAl{sub 2}O{sub 4} additions

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Zongliang, E-mail: zzlma@163.com; Zhang, Huaiwu; Yang, Qinghui; Jia, Lijun

    2015-11-05

    In this study, nanocrystalline ZnAl{sub 2}O{sub 4} (ZA) (x = 0–20 wt%) were introduced into Ni{sub 0.4}Zn{sub 0.6}Fe{sub 2}O{sub 4} ferrite (NZ) by a solid-state reaction method combining a sol–gel auto-combustion method. The effects of ZA addition on the crystalline phase formation, microstructures, magnetic and dielectric properties were systematically investigated. X-ray diffraction and scanning electron microscope results reveal that the added ZA can fully solve into the NZ to form a ceramic with single-phase cubic spinel structure, and the grain size decreases obviously as x > 5 wt%. Meanwhile, the magnetic and dielectric properties exhibit significantly dependent on the ZA addition content. With the increasing addition level of ZA from 0 to 20 wt%, the initial permeability μ{sub i} is found increased initially and then decreased with the maximum 679 at x = 0.5 wt%. For the samples with x ≤ 5 wt%, permittivity ε′ is relatively higher at low frequencies (ε′ = 91–138 at 1 MHz) and dielectric loss tan δ{sub ε} shows distinct peak behavior. When x reaches 10 wt%, however, the ε′ and tan δ{sub ε} show very stable spectra from 1 MHz to 1 GHz. - Highlights: • Various amount of nanocrystalline ZnAl{sub 2}O{sub 4} (ZA) were introduced into NiZn ferrite. • NiZn ferrite can form single-phase spinel ceramic materials with ZA additives. • ZA has significant effects on magnetic and dielectric properties of the ceramics. • It provides a new method for fabricating NiZn ferrite with tunable properties.

  9. A comparative study of the physical and chemical properties of nano-sized ZnO particles from multiple batches of three commercial products

    Energy Technology Data Exchange (ETDEWEB)

    Yin, Hong [Commonwealth Scientific and Industrial Research Organisation, Manufacturing Flagship (Australia); Coleman, Victoria A. [National Measurement Institute Australia, Nanometrology Section (Australia); Casey, Phil S., E-mail: Phil.Casey@csiro.au [Commonwealth Scientific and Industrial Research Organisation, Manufacturing Flagship (Australia); Angel, Brad [Commonwealth Scientific and Industrial Research Organisation, Land and Water Flagship (Australia); Catchpoole, Heather J. [National Measurement Institute Australia, Nanometrology Section (Australia); Waddington, Lynne [Commonwealth Scientific and Industrial Research Organisation, Manufacturing Flagship (Australia); McCall, Maxine J. [Commonwealth Scientific and Industrial Research Organisation, Food and Nutrition Flagship (Australia)

    2015-02-15

    Given the broad commercial applications for ZnO nanomaterials, accurate attribution of physicochemical characteristics that induce toxic effects is particularly important. We report on the physicochemical properties of three commercial nano-ZnO products: Z-COTE and Z-COTE HP1 from BASF, and Nanosun from Micronisers, and, for reference, “bulk” ZnO from Sigma-Aldrich. Z-COTE, Nanosun and “bulk” consist of uncoated particles with different sizes, while Z-COTE HP1 consists of nanoparticles with a hydrophobic coating. Specific batches of these ZnO products were included in the OECD Sponsorship Programme to test manufactured nanomaterials. In order to identify properties potentially susceptible to variations between production runs, three additional batches of Z-COTE and Nanosun and two additional batches of Z-COTE HP1 were also investigated here. In general, all products showed little variation between batches for properties measured from powdered samples, but batch variations in the amount of surface coating were evident for the coated Z-COTE HP1. Properties measured with samples dispersed in liquids (agglomeration, photocatalytic activity, dissolution) were highly dependent on dispersion protocols, and this made it difficult to differentiate between differences due to dispersion and due to batches. However, batch-sensitive properties did appear to be present in Z-COTE and Z-COTE HP1 (photocatalytic activity), and Nanosun (dissolution). Intra-batch time and/or storage-dependent changes in the applied surface coating, noted specifically for the OECD batch of Z-COTE HP1, highlight the need for best practice when storing and accessing stocks of nano products. Awareness of inter-batch and intra-batch variability is essential for commercial applications and for nanotoxicological studies aimed at identifying links between physicochemical properties and any adverse effects in biological systems.

  10. A comparative study of the physical and chemical properties of nano-sized ZnO particles from multiple batches of three commercial products

    Science.gov (United States)

    Yin, Hong; Coleman, Victoria A.; Casey, Phil S.; Angel, Brad; Catchpoole, Heather J.; Waddington, Lynne; McCall, Maxine J.

    2015-02-01

    Given the broad commercial applications for ZnO nanomaterials, accurate attribution of physicochemical characteristics that induce toxic effects is particularly important. We report on the physicochemical properties of three commercial nano-ZnO products: Z-COTE and Z-COTE HP1 from BASF, and Nanosun from Micronisers, and, for reference, "bulk" ZnO from Sigma-Aldrich. Z-COTE, Nanosun and "bulk" consist of uncoated particles with different sizes, while Z-COTE HP1 consists of nanoparticles with a hydrophobic coating. Specific batches of these ZnO products were included in the OECD Sponsorship Programme to test manufactured nanomaterials. In order to identify properties potentially susceptible to variations between production runs, three additional batches of Z-COTE and Nanosun and two additional batches of Z-COTE HP1 were also investigated here. In general, all products showed little variation between batches for properties measured from powdered samples, but batch variations in the amount of surface coating were evident for the coated Z-COTE HP1. Properties measured with samples dispersed in liquids (agglomeration, photocatalytic activity, dissolution) were highly dependent on dispersion protocols, and this made it difficult to differentiate between differences due to dispersion and due to batches. However, batch-sensitive properties did appear to be present in Z-COTE and Z-COTE HP1 (photocatalytic activity), and Nanosun (dissolution). Intra-batch time and/or storage-dependent changes in the applied surface coating, noted specifically for the OECD batch of Z-COTE HP1, highlight the need for best practice when storing and accessing stocks of nano products. Awareness of inter-batch and intra-batch variability is essential for commercial applications and for nanotoxicological studies aimed at identifying links between physicochemical properties and any adverse effects in biological systems.

  11. Morphological and structural characterization of the Zn0,9Mn0,1O powder synthesized by combustion reaction and Pechini

    International Nuclear Information System (INIS)

    Ribeiro, M.A.; Torquato, R.; Simoes, A.N.; Costa, A.C.F.M.; Gama, L.; Kiminami, R.H.G.A.

    2009-01-01

    Zinc oxide, due to the piezoelectric and electro-optical characteristics, is used in application such as, chemical sensor, varistor, transparent conductive thin film and DMS. The aim of this work is to evaluate and compare structural and morphological characteristics of nanometric powders of Zn 0,9 Mn 0,1 O prepared by chemical synthesis of combustion reaction and Pechini method. The powders were characterized by XRD, SEM and BET. The XRD data shown to both studied method the presence of ZnO phase with hexagonal structure and without second phase. The powder prepared by combustion reaction presented 9% of reduction in crystallinity and 42% of increase in surface area in comparison with the powder prepared by Pechini method. The morphological analysis of the powder showed that both method produce powders with soft agglomerates constituted by nano size particles. (author)

  12. Spectrum designation and effect of Al substitution on the luminescence of Cr{sup 3+} doped ZnGa{sub 2}O{sub 4} nano-sized phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Weiwei [Key Laboratory of Micro-nano Measurement, Manipulation and Physics (Ministry of Education), School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Zhang Junying, E-mail: zjy@buaa.edu.c [Key Laboratory of Micro-nano Measurement, Manipulation and Physics (Ministry of Education), School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Chen Ziyu; Wang Tianmin [Key Laboratory of Micro-nano Measurement, Manipulation and Physics (Ministry of Education), School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Zheng Shukai [College of Electronic and Information Engineering, Hebei University, Baoding 071200 (China)

    2010-10-15

    Low-temperature photoluminescent spectra of ZnGa{sub 2}O{sub 4}:Cr{sup 3+} nano-sized phosphors calcined at different temperatures were reported. The fine structure of the emission spectra has been designated to Cr{sup 3+} ions in different sites including ideal octahedral, Zn-interstitial, Ga{sub ZN}{sup 4}-Zn{sub Ga}{sup 6} sites and Ga{sub 2}O{sub 3} impurity. The vibronic sidebands for both Stokes' and anti-Stokes' sides are related to the host lattice vibrations, which were confirmed by IR and Raman spectra. Al{sup 3+} is substituted in Ga{sup 3+} sites to form Zn(Ga{sub 1-y}Al{sub y}){sub 2}O{sub 4}:Cr{sub 0.01}{sup 3+} (0{<=}y{<=}0.5). The blue shift and luminescent intensity variations of the charge transfer band and 3d-3d transitions in the spectra caused by Al substitution were related to larger band gap and stronger crystal field, respectively. The calculated crystal-field parameters indicated that Al incorporation enhanced the crystal field strength and induced more trigonal distortion due to different radii of Al{sup 3+} and Ga{sup 3+}.

  13. The effect of nano-size ZrO2 powder addition on the microstructure and superconducting properties of single-domain Y-Ba-Cu-O bulk superconductors

    International Nuclear Information System (INIS)

    Iida, K; Babu, N H; Reddy, E S; Shi, Y-H; Cardwell, D A

    2005-01-01

    The effect of nano-size ZrO 2 powder addition on the microstructure and superconducting properties of Y-Ba-Cu-O single grain bulk superconductors has been investigated. Significant pushing phenomena of Y 2 BaCuO 5 (Y-211) particles, particularly in the c growth sector, were observed even with a small amount of ZrO 2 added to the precursor powder. An increase in Y-211 particle pushing was observed with increasing ZrO 2 content, leading to an inhomogeneous bulk microstructure. In addition, a growth cycle consisting of a Y-211 free layer-porous narrow layer-Y-211 high concentration layer was observed for samples prepared with 0.25 wt% ZrO 2 in both the a and c growth sectors. The extent of the growth of single grain Y-Ba-Cu-O (YBCO) decreased with increasing ZrO 2 content due to increased pushing of Y-211 particles towards molten liquid. The superconducting transition temperature, T c , of the ZrO 2 containing YBCO samples was sharp but depressed slightly (by up to 1 K) compared with an undoped YBCO grain, indicating a relative insensitivity of T c to ZrO 2 content. Finally, the sensitivity of critical current density, J c , to applied magnetic field in large grain bulk YBCO containing ZrO 2 was observed to depend critically on position due to the inhomogeneous sample microstructure

  14. Morphological and structural characterization of the Zn{sub 0,9}Mn{sub 0,1}O powder synthesized by combustion reaction and Pechini; Caracterizacao estrutural e morfologica de pos de Zn{sub 0,9}Mn{sub 0,1}O sintetizados por reacao de combustao e metodo Pechini

    Energy Technology Data Exchange (ETDEWEB)

    Ribeiro, M A; Torquato, R; Simoes, A N; Costa, A C.F.M.; Gama, L [Universidade Federal de Campina Grande (DEMA/UFCG), PB (Brazil). Dept. de Engenharia dos Materiais; Kiminami, R H.G.A. [Universidade Federal de Sao Carlos (DEMA/UFSCar), SP (Brazil). Dept. de Engenharia de Materiais

    2009-07-01

    Zinc oxide, due to the piezoelectric and electro-optical characteristics, is used in application such as, chemical sensor, varistor, transparent conductive thin film and DMS. The aim of this work is to evaluate and compare structural and morphological characteristics of nanometric powders of Zn{sub 0,9}Mn{sub 0,1}O prepared by chemical synthesis of combustion reaction and Pechini method. The powders were characterized by XRD, SEM and BET. The XRD data shown to both studied method the presence of ZnO phase with hexagonal structure and without second phase. The powder prepared by combustion reaction presented 9% of reduction in crystallinity and 42% of increase in surface area in comparison with the powder prepared by Pechini method. The morphological analysis of the powder showed that both method produce powders with soft agglomerates constituted by nano size particles. (author)

  15. Highly Efficient Defect Emission from ZnO:Zn and ZnO:S Powders

    Science.gov (United States)

    Everitt, Henry

    2013-03-01

    Bulk Zinc Oxide (ZnO) is a wide band gap semiconductor with an ultraviolet direct band gap energy of 3.4 eV and a broad, defect-related visible wavelength emission band centered near 2 eV. We have shown that the external quantum efficiency can exceed 50% for this nearly white emission band that closely matches the human dark-adapted visual response. To explore the potential of ZnO as a rare earth-free white light phosphor, we investigated the mechanism of efficient defect emission in three types of ZnO powders: unannealed, annealed, and sulfur-doped. Annealing and sulfur-doping of ZnO greatly increase the strength of defect emission while suppressing the UV band edge emission. Continuous wave and ultrafast one- and two-photon excitation spectroscopy are used to examine the defect emission mechanism. Low temperature photoluminescence (PL) and PL excitation (PLE) spectra were measured for all three compounds, and it was found that bound excitons mediate the defect emission. Temperature-dependent PLE spectra for the defect and band edge emission were measured to estimate trapping and activation energies of the bound excitons and clarify the role they play in the defect emission. Time-resolved techniques were used to ascertain the role of exciton diffusion, the effects of reabsorption, and the spatial distributions of radiative and non-radiative traps. In unannealed ZnO we find that defect emission is suppressed and UV band edge emission is inefficient (reduced, and a high density of defects responsible for the broad visible emission are created near the surface. Interestingly, nearly identical PLE spectra are found for both the band edge and the defect emission, one of many indications that the defect emission is deeply connected to bound excitons. Quantum efficiency, also measured as a function of excitation wavelength, closely mirrors the PLE spectra for both emission bands. Sulfur-doped ZnO exhibits additional PLE and X-ray features indicative of a ZnS-rich surface

  16. Effect of nano size 3% wt TaC particles dispersion in two different metallic matrix composites

    International Nuclear Information System (INIS)

    Gomes, U.U.; Oliveira, L.A.; Souza, C.P.; Menezes, R.C.; Furukava, M.; Torres, Y.

    2009-01-01

    This work studies the characteristics of two different metallic matrixes composites, ferritic and austenitic steels, reinforced with 3% wt nano size tantalum carbide by powder metallurgy. The starting powders were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The effects of the nano sized carbide dispersion on the matrix microstructures and its consequences on the mechanical properties were identified. The preliminary results showed that the sintering were influenced by morphology and the distribution of carbide and the alloys. (author)

  17. Sonochemical synthesis and characterization of nano-sized zinc(II coordination complex as a precursor for the preparation of pure-phase zinc(II oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Maryam Ranjbar

    2017-01-01

    Full Text Available In current study, nanoparticles and single crystals of a Zn(II coordination complex, [Zn(dmphI2](1, {dmph=2,9-dimethyl-1,10-phenanthroline(neocuproine}, have been synthesized by the reaction of zinc(II acetate, KI and neocuproine as ligand in methanol using sonochemical and heat gradient methods, respectively. The nanostructure of 1 was characterized by scanning electron microscopy (SEM, X-ray powder diffraction (XRD, FT-IR spectroscopy and elemental analyses, and the structure of compound 1 was determined by single-crystal X-ray diffraction. The thermal stability of nano-sized 1 has been studied by thermogravimetric (TG and differential thermal analyses (DTA. Structural determination of compound 1 reveals the Zn(II ion is four-coordinated in a distorted tetrahedral configuration by two N atoms from a 2,9-dimethyl-1,10-Phenanthroline ligand and two terminal I atoms. The effect of supercritical condition on stability, size and morphology of nano-structured compound 1 has also been studied. The XRD pattern of the residue obtained from thermal decomposition of nano-sized compound 1 at 600 °C under air atmosphere provided pure phase of ZnO with the average particles size of about 31 nm.

  18. Thermoluminescent properties of ZnS:Mn nanocrystalline powders

    International Nuclear Information System (INIS)

    Ortiz-Hernández, Arturo Agustín; Méndez García, Víctor Hugo; Pérez Arrieta, María Leticia; Ortega Sígala, José Juan

    2015-01-01

    Thermoluminescent ZnS nanocrystals doped with Mn 2+ ions were synthesized by chemical co-precipitation method. From X-ray diffraction studies it was observed that the synthesized nanoparticles have cubic zinc blende structure with average sizes of about 40–50 nm. Morphology was analyzed by TEM. Photoluminescence studies showed two transitions, one of them close to 396 nm and other close to 598 nm, which is enhanced with increasing dopant concentration, this behavior was also observed in the cathodoluminescence spectrum. The thermoluminescence gamma dose-response has linear behavior over dose range 5–100 mGy, the glow curve structure shows two glow peaks at 436 K and at 518 K that were taken into account to calculate the kinetic parameters using the Computerized Glow Curve Deconvolution procedure. - Highlights: • Nanocrystals in powder of ZnS:Mn were synthesized using the co-precipitation method. • The integrated TL spectra has a linear behavior on the dose range 5–100 mGy of γ-radiation. • The kinetic parameters were obtained by the CGCD procedure. • Results support the possible use of nanocrystalline ZnS:Mn as a new γ-dose nanoTLD

  19. Study on preparation and properties of molybdenum alloys reinforced by nano-sized ZrO{sub 2} particles

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Chaopeng; Gao, Yimin; Zhou, Yucheng [Xi' an Jiaotong University, State Key Laboratory for Mechanical Behavior of Materials, Xi' an, Shaanxi Province (China); Wei, Shizhong [Henan University of Science and Technology, School of Materials Science and Engineering, Luoyang (China); Henan University of Science and Technology, Engineering Research Center of Tribology and Materials Protection, Ministry of Education, Luoyang (China); Zhang, Guoshang; Zhu, Xiangwei; Guo, Songliang [Henan University of Science and Technology, School of Materials Science and Engineering, Luoyang (China)

    2016-03-15

    The nano-sized ZrO{sub 2}-reinforced Mo alloy was prepared by a hydrothermal method and a subsequent powder metallurgy process. During the hydrothermal process, the nano-sized ZrO{sub 2} particles were added into the Mo powder via the hydrothermal synthesis. The grain size of Mo powder decreases obviously with the addition of ZrO{sub 2} particles, and the fine-grain sintered structure is obtained correspondingly due to hereditation. In addition to a few of nano-sized ZrO{sub 2} particles in grain boundaries or sub-boundaries, most are dispersed in grains. The tensile strength and yield strength have been increased by 32.33 and 53.76 %. (orig.)

  20. Study on preparation and properties of molybdenum alloys reinforced by nano-sized ZrO2 particles

    International Nuclear Information System (INIS)

    Cui, Chaopeng; Gao, Yimin; Zhou, Yucheng; Wei, Shizhong; Zhang, Guoshang; Zhu, Xiangwei; Guo, Songliang

    2016-01-01

    The nano-sized ZrO 2 -reinforced Mo alloy was prepared by a hydrothermal method and a subsequent powder metallurgy process. During the hydrothermal process, the nano-sized ZrO 2 particles were added into the Mo powder via the hydrothermal synthesis. The grain size of Mo powder decreases obviously with the addition of ZrO 2 particles, and the fine-grain sintered structure is obtained correspondingly due to hereditation. In addition to a few of nano-sized ZrO 2 particles in grain boundaries or sub-boundaries, most are dispersed in grains. The tensile strength and yield strength have been increased by 32.33 and 53.76 %. (orig.)

  1. Preparation of nanometer sized Mn doped Zn based oxides powder for DMS applications

    CSIR Research Space (South Africa)

    Das, J

    2009-01-01

    Full Text Available In order to study the size dependent DMS (Diluted Magnetic Semiconductor) behavior of Mn doped ZnO, the authors have systematically prepared a series of nanosized green powder based on Mn doped ZnO (Zn 1-x Mn x O, where x=0.02 - 0.1) materials using...

  2. Microstructure of Multi-Pass Friction-Stir-Processed Al-Zn-Mg-Cu Alloys Reinforced by Nano-Sized TiB2 Particles and the Effect of T6 Heat Treatment

    Directory of Open Access Journals (Sweden)

    Xiaofei Ju

    2017-11-01

    Full Text Available In this work, a fine-grained structure with a uniform distribution of TiB2 particles and precipitates was achieved in TiB2 particle-reinforced (PR Al-Zn-Mg-Cu alloys by friction stir processing (FSP. The effects of multi-pass FSP on the microstructure, and TiB2 particle distribution, as well as the microstructural evolution in the following T6 treatment, were investigated by X-ray diffraction, scanning electron microscopy and associated electron backscattered diffraction. The results showed that the distribution of TiB2 particles and alloy precipitates was further improved with an increase in the FSP passes. Moreover, compared with alloy segregation in the as-cast PR alloys during T6 treatment, a complete solution of the precipitates was achieved in the FSP-treated PR alloys. The fine-grained structure of the FSP-treated PR alloys was thermally stable without any abnormal growth at the high temperature of T6 treatment due to the pinning effect of dispersed TiB2 particles. The strength and ductility of the PR alloys were simultaneously improved by the combination of FSP and T6 treatment.

  3. Molten salt synthesis of ZnNb2O6 powder

    International Nuclear Information System (INIS)

    Guo Liangzhai; Dai Jinhui; Tian Jintao; Zhu Zhibin; He Tian

    2007-01-01

    Pure ZnNb 2 O 6 powder was successfully prepared by the molten salt synthesis method using Nb 2 O 5 and ZnO as raw materials and a mixture of NaCl and KCl as the solvent. The phase form and morphology of the prepared powder were characterized by X-ray diffraction and scanning electron microscopy. The effect of reacting temperature on phase formation was investigated. The results indicated that the single phase ZnNb 2 O 6 powder can be obtained by the molten salt synthesis method at 600 deg. C, and the SEM photographs show that the grains of the powder are rod-like particles

  4. Structural and optical analysis of ZnBeMgO powder and thin films

    International Nuclear Information System (INIS)

    Panwar, Neeraj; Liriano, J.; Katiyar, Ram S.

    2011-01-01

    Research highlights: → Structural and optical studies of Zn 1-x-y Be x Mg y O (0 ≤ x ≤0.10; 0 ≤ y ≤ 0.20) powders and thin films. → Raman studies of the pure ZnO powder showed all the characteristic peaks of the wurtzite hexagonal structure and with (Be, Mg) co-doping new modes appeared which can be attributed to arise as a result of doping effect. → The XRD of the films prepared from the powders using pulsed laser deposition (PLD) technique exhibited the preferential orientation and with doping the (0 0 0 2) peak also shifts to higher 2θ values suggesting the incorporation of Be/Mg at the Zn-site. → From the UV-visible optical band gap measurement it was noticed that the band gap of the pristine ZnO film is 3.3 eV which enhanced up to 4.51 eV for Zn 0.7 Be 0.1 Mg 0.2 O film which lies in the solar blind region and is very useful for the deep UV detection. - Abstract: We here report the structural and optical studies of Zn 1-x-y Be x Mg y O (0 ≤ x ≤ 0.15; 0 ≤ y ≤ 0.20) powders and thin films. From the Rietveld refinement of the powder X-ray diffraction (XRD) patterns it was revealed that the value of 'a' lattice parameter remains almost unchanged whereas 'c' parameter reduces with Be and Mg co-doping in ZnO. The Zn-O bond length also decreases in co-doped samples. Raman studies of the pure ZnO powder showed all the characteristic peaks of the wurtzite hexagonal structure and with (Be, Mg) co-doping new modes appeared which can be attributed to arise as a result of substitution. The XRD of the films prepared from the powders using pulsed laser deposition (PLD) technique exhibited the preferential orientation and with increase in co-doping the (0 0 0 2) peak also shifts to higher 2θ values suggesting the incorporation of Be/Mg at the Zn-site. From the UV-visible optical transmittance measurement it was noticed that the band gap of the pristine ZnO film is 3.3 eV which enhanced up to 4.51 eV for Zn 0.7 Be 0.1 Mg 0.2 O film which lies in the

  5. The synthesis and characterization of Mg-Zn-Ca alloy by powder metallurgy process

    Energy Technology Data Exchange (ETDEWEB)

    Annur, Dhyah; Franciska, P.L.; Erryani, Aprilia; Amal, M. Ikhlasul; Kartika, Ika, E-mail: pepeng2000@yahoo.com [Research center for Metallurgy and Material, Indonesian Institute of Science (Indonesia); Sitorus, Lyandra S. [Sultan Ageng Tirtayasa University (Indonesia)

    2016-04-19

    Known for its biodegradation and biocompatible properties, magnesium alloys have gained many interests to be researched as implant material. In this study, Mg-3Zn-1Ca, Mg-29Zn-1Ca, and Mg-53Zn-4.3Ca (in wt%) were synthesized by means of powder metallurgy method. The compression strength and corrosion resistance of magnesium alloy were thoroughly examined. The microstructures of the alloy were characterized using optical microscopy, Scanning Electron Microscope, and also X-ray diffraction analysis. The corrosion resistance were evaluated using electrochemical analysis. The result indicated that Mg- Zn- Ca alloy could be synthesized using powder metallurgy method. This study showed that Mg-29Zn-1Ca would make the highest mechanical strength up to 159.81 MPa. Strengthening mechanism can be explained by precipitation hardening and grain refinement mechanism. Phase analysis had shown the formation of α Mg, MgO, and intermetallic phases: Mg2Zn11 and also Ca2Mg6Zn3. However, when the composition of Zn reach 53% weight, the mechanical strength will be decreasing. In addition, all of Mg-Zn-Ca alloy studied here had better corrosion resistance (Ecorr around -1.4 VSCE) than previous study of Mg. This study indicated that Mg- 29Zn- 1Ca alloy can be further analyzed to be a biodegradable implant material.

  6. Microwave assisted synthesis of nano sized sulphate doped hydroxyapatite

    Energy Technology Data Exchange (ETDEWEB)

    Alshemary, Ammar Z.; Goh, Yi-Fan; Akram, Muhammad; Razali, Ili Rabihah [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Skudai, Johor Darul Ta’zim (Malaysia); Abdul Kadir, Mohammed Rafiq [Medical Implant Technology Group, Faculty of Biomedical Engineering and Health Science, Universiti Teknologi Malaysia,81310 UTM Skudai, Johor Darul Ta’zim (Malaysia); Hussain, Rafaqat, E-mail: rafaqat@kimia.fs.utm.my [Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia, 81310 UTM Skudai, Johor DarulTa’zim (Malaysia)

    2013-06-01

    Highlights: ► Phase pure nano-sized sulphur doped hydroxyapatite has been synthesized. ► TEM analysis confirmed formation of needle shaped structure. ► Lattice parameters and cell volume increased with increase in sulphate doping. ► Crystallite size decreased as sulphate content inside the structure increased. ► Degree of crystallinity decreased with increase in sulphate substitution. - Abstract: Inorganic sulphate is required by all mammalian cells to function properly, it is the fourth most abundant anion in the human plasma. Sulphate ions are the major source of sulphur which is considered an important element for sustenance of life as it is present in the essential amino and is required by cells to function properly. In this study we have successfully substituted sulphate ions (SO{sub 4}{sup 2−}) into hydroxyapatite (Ca{sub 10}(PO{sub 4}){sub 6−x}(SO{sub 4}){sub x}(OH){sub 2−x}) lattice via ion exchange process with phosphate group. Concentration of SO{sub 4}{sup 2−} ions was varied between X = 0.05–0.5, using (Ca (NO{sub 3}){sub 2}·4H{sub 2}O), ((NH{sub 4}){sub 2}HPO{sub 4}) and (Na{sub 2}SO{sub 4}) as starting materials. X-ray diffraction (XRD), Fourier transform IR spectroscopy (FTIR), showed that the substitution of SO{sub 4}{sup 2−} ions into the lattice resulted in peak broadening and reduced peak height due to the amorphous nature and reduced crystallinity of the resulting HA powder. Transmission electron microscopy (TEM) and field emission electron microscopy (FESEM) analysis confirmed the formation of needle shaped particles of 41 nm size with homogenous and uniform distribution of element within the HA structure.

  7. Microwave assisted synthesis of nano sized sulphate doped hydroxyapatite

    International Nuclear Information System (INIS)

    Alshemary, Ammar Z.; Goh, Yi-Fan; Akram, Muhammad; Razali, Ili Rabihah; Abdul Kadir, Mohammed Rafiq; Hussain, Rafaqat

    2013-01-01

    Highlights: ► Phase pure nano-sized sulphur doped hydroxyapatite has been synthesized. ► TEM analysis confirmed formation of needle shaped structure. ► Lattice parameters and cell volume increased with increase in sulphate doping. ► Crystallite size decreased as sulphate content inside the structure increased. ► Degree of crystallinity decreased with increase in sulphate substitution. - Abstract: Inorganic sulphate is required by all mammalian cells to function properly, it is the fourth most abundant anion in the human plasma. Sulphate ions are the major source of sulphur which is considered an important element for sustenance of life as it is present in the essential amino and is required by cells to function properly. In this study we have successfully substituted sulphate ions (SO 4 2− ) into hydroxyapatite (Ca 10 (PO 4 ) 6−x (SO 4 ) x (OH) 2−x ) lattice via ion exchange process with phosphate group. Concentration of SO 4 2− ions was varied between X = 0.05–0.5, using (Ca (NO 3 ) 2 ·4H 2 O), ((NH 4 ) 2 HPO 4 ) and (Na 2 SO 4 ) as starting materials. X-ray diffraction (XRD), Fourier transform IR spectroscopy (FTIR), showed that the substitution of SO 4 2− ions into the lattice resulted in peak broadening and reduced peak height due to the amorphous nature and reduced crystallinity of the resulting HA powder. Transmission electron microscopy (TEM) and field emission electron microscopy (FESEM) analysis confirmed the formation of needle shaped particles of 41 nm size with homogenous and uniform distribution of element within the HA structure

  8. Corrosion behaviour of powder metallurgical and cast Al-Zn-Mg base alloys

    International Nuclear Information System (INIS)

    Sameljuk, A.V.; Neikov, O.D.; Krajnikov, A.V.; Milman, Yu.V.; Thompson, G.E.

    2004-01-01

    The behaviour of Al-Zn-Mg base alloys produced by powder metallurgy and casting has been studied using potentiodynamic polarisation in 0.3% and 3% NaCl solutions. The influence of alloy production route on microstructure has been examined by scanning electron microscopy, Auger electron spectroscopy and secondary ion mass spectrometry. An improvement in performance of powder metallurgy (PM) materials, compared with the cast alloy, was evident in solutions of low chloride concentration; less striking differences were revealed in high chloride concentration. Both powder metallurgy and cast alloys show two main types of precipitates, which were identified as Zn-Mg and Zr-Sc base intermetallic phases. The microstructure of the PM alloys is refined compared with the cast material, which assists understanding of the corrosion performance. The corrosion process commences with dissolution of the Zn-Mg base phases, with the relatively coarse phases present in the cast alloy showing ready development of corrosion

  9. Nano-sized cosmetic formulations or solid nanoparticles in sunscreens: a risk to human health?

    Science.gov (United States)

    Nohynek, Gerhard J; Dufour, Eric K

    2012-07-01

    Personal care products (PCP) often contain micron- or nano-sized formulation components, such as nanoemulsions or microscopic vesicles. A large number of studies suggest that such vesicles do not penetrate human skin beyond the superficial layers of the stratum corneum. Nano-sized PCP formulations may enhance or reduce skin absorption of ingredients, albeit at a limited scale. Modern sunscreens contain insoluble titanium dioxide (TiO₂) or zinc oxide (ZnO) nanoparticles (NP), which are efficient filters of UV light. A large number of studies suggest that insoluble NP do not penetrate into or through human skin. A number of in vivo toxicity tests, including in vivo intravenous studies, showed that TiO₂ and ZnO NP are non-toxic and have an excellent skin tolerance. Cytotoxicity, genotoxicity, photo-genotoxicity, general toxicity and carcinogenicity studies on TiO₂ and ZnO NP found no difference in the safety profile of micro- or nano-sized materials, all of which were found to be non-toxic. Although some published in vitro studies on insoluble nano- or micron-sized particles suggested cell uptake, oxidative cell damage or genotoxicity, these data are consistent with those from micron-sized particles and should be interpreted with caution. Data on insoluble NP, such as surgical implant-derived wear debris particles or intravenously administered magnetic resonance contrast agents suggest that toxicity of small particles is generally related to their chemistry rather than their particle size. Overall, the weight of scientific evidence suggests that insoluble NP used in sunscreens pose no or negligible risk to human health, but offer large health benefits, such as the protection of human skin against UV-induced skin ageing and cancer.

  10. In vitro study of nano-sized zinc doped bioactive glass

    Energy Technology Data Exchange (ETDEWEB)

    Goh, Yi-Fan; Alshemary, Ammar Z.; Akram, Muhammad [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM skudai, Johor Darul Ta' zim (Malaysia); Abdul Kadir, Mohammed Rafiq [Medical Implant Technology Group, Faculty of Biomedical Engineering and Health Science, Universiti Teknologi Malaysia, 81310 UTMJohor Bahru (Malaysia); Hussain, Rafaqat, E-mail: rafaqat@kimia.fs.utm.my [IbnuSina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor DarulTa' zim (Malaysia)

    2013-01-15

    Surface reactivity in physiological fluid has been linked to bioactivity of a material. Past research has shown that bioactive glass containing zinc has the potential in bone regeneration field due to its enhanced bioactivity. However, results from literature are always contradictory. Therefore, in this study, surface reactivity of bioactive glass containing zinc was evaluated through the study of morphology and composition of apatite layer formed after immersion in simulated body fluid (SBF). Nano-sized bioactive glass with 5 and 10 mol% zinc were synthesized through quick alkali sol-gel method. The synthesized Zn-bioglass was characterized using field emission scanning electron microscope (FESEM), energy dispersive X-ray spectrometer (EDX), X-ray diffractometer (XRD) and Fourier transform infrared spectrometer (FTIR). Samples after SBF immersion were characterized using scanning electron microscope (SEM) and EDX. Morphological study through SEM showed the formation of spherical apatite particles with Ca/P ratio closer to 1.67 on the surface of 5 mol% Zn-bioglass. Whereas, the 10 mol% Zn-bioglass samples induced the formation of flake-like structure of calcite in addition to the spherical apatite particles with much higher Ca/P ratio. Our results suggest that the higher Zn content increases the bioactivity through the formation of bone-bonding calcite as well as the spherical apatite particles. -- Highlights: Black-Right-Pointing-Pointer Nano-sized bioactive glasses were synthesized through quick alkali sol-gel method. Black-Right-Pointing-Pointer 5 and 10 mol% Zn-bioglass induced the formation of spherical particles in SBF test. Black-Right-Pointing-Pointer 10 mol% Zn-bioglass also induced the formation of flake-like structure. Black-Right-Pointing-Pointer The flake-like structure is calcium carbonate; spherical particles are apatite. Black-Right-Pointing-Pointer High Zn contents negatively influence the chemical composition of the apatite layer.

  11. Evaluation of Sintering Behavior of Premix Al-Zn-Mg-Cu Alloy Powder

    Directory of Open Access Journals (Sweden)

    Haris Rudianto

    2015-01-01

    Full Text Available Sintering of light aluminium alloys powder has been investigated as a way to substitute steels in automotive and aerospace industries. Premix Al-5.5Zn-2.5Mg-0.5Cu composite powder called Alumix 431D was analyzed in this research. Sintering was carried out under ultra high purity nitrogen gas and before reaching sintering temperature, green samples were delubricated at 400°C for 30 min. The powder possesses high sinterability by reaching 96% relative density at 580°C sintering temperature. Formation of liquid phase seems to support achieving high sintering density. Optimum mechanical properties also were obtained under those conditions. T6 heat treatment was done to improve the mechanical properties by formation of precipitation strengthening, and MgZn2 appears to be dominant strengthening precipitate. X-ray diffraction, optical microscopy, and SEM-EDS were used to characterize powder, and sintered and heat treated samples.

  12. Al-doped ZnO mechanical milled powders for dye sensitized cells

    International Nuclear Information System (INIS)

    Damonte, L.C.; Donderis, V.; Ferrari, S.; Orozco, J.; Hernandez-Fenollosa, M.A.

    2010-01-01

    Mixtures of Al 2 O 3 and ZnO powders were prepared by mechanical milling. The resulting samples were analyzed and characterized by X-ray diffraction (XRD), positron annihilation lifetime spectroscopy (PALS), scanning electron microscopy (SEM) and optical reflection spectroscopy (OPS). XRD and PALS measurements confirm Al incorporation into ZnO wurtzite structure. Powders obtained from Al 2 O 3 precursors display better reflectivity than those prepared from Al metal so they might be better materials for implementation in photovoltaic solar devices.

  13. Al-doped ZnO mechanical milled powders for dye sensitized cells

    Energy Technology Data Exchange (ETDEWEB)

    Damonte, L.C., E-mail: damonte@fisica.unlp.edu.a [Departamento de Fisica, UNLP, IFLP-CCT-CONICET, C.C.67(1900), La Plata (Argentina); Dto. de Fisica Aplicada, Universidad Politecnica de Valencia, Cami de Vera s/n, 46022 Valencia (Spain); Donderis, V. [Dto. de Ingenieria Electrica, Universidad Politecnica de Valencia, Cami de Vera s/n, 46022 Valencia (Spain); Ferrari, S. [Departamento de Fisica, UNLP, IFLP-CCT-CONICET, C.C.67(1900), La Plata (Argentina); Orozco, J. [ITM, Universidad Politecnica de Valencia, Cami de Vera s/n, 46022 Valencia (Spain); Hernandez-Fenollosa, M.A. [Dto. de Fisica Aplicada, Universidad Politecnica de Valencia, Cami de Vera s/n, 46022 Valencia (Spain)

    2010-04-16

    Mixtures of Al{sub 2}O{sub 3} and ZnO powders were prepared by mechanical milling. The resulting samples were analyzed and characterized by X-ray diffraction (XRD), positron annihilation lifetime spectroscopy (PALS), scanning electron microscopy (SEM) and optical reflection spectroscopy (OPS). XRD and PALS measurements confirm Al incorporation into ZnO wurtzite structure. Powders obtained from Al{sub 2}O{sub 3} precursors display better reflectivity than those prepared from Al metal so they might be better materials for implementation in photovoltaic solar devices.

  14. Structure and properties of ZnSxSe1-x thin films deposited by thermal evaporation of ZnS and ZnSe powder mixtures

    Science.gov (United States)

    Valeev, R. G.; Romanov, E. A.; Vorobiev, V. L.; Mukhgalin, V. V.; Kriventsov, V. V.; Chukavin, A. I.; Robouch, B. V.

    2015-02-01

    Interest to ZnSxSe1-x alloys is due to their band-gap tunability varying S and Se content. Films of ZnSxSe1-x were grown evaporating ZnS and ZnSe powder mixtures onto SiO2, NaCl, Si and ITO substrates using an original low-cost method. X-ray diffraction patterns and Raman spectroscopy, show that the lattice structure of these films is cubic ZnSe-like, as S atoms replace Se and film compositions have their initial S/Se ratio. Optical absorption spectra show that band gap values increase from 2.25 to 3 eV as x increases, in agreement with the literature. Because S atomic radii are smaller than Se, EXAFS spectra confirm that bond distances and Se coordination numbers decrease as the Se content decreases. The strong deviation from linearity of ZnSe coordination numbers in the ZnSxSe1-x indicate that within this ordered crystal structure strong site occupation preferences occur in the distribution of Se and S ions. The behavior is quantitatively confirmed by the strong deviation from the random Bernoulli distribution of the three sight occupation preference coefficients of the strained tetrahedron model. Actually, the ternary ZnSxSe1-x system is a bi-binary (ZnS+ZnSe) alloy with evanescent formation of ternary configurations throughout the x-range.

  15. Fabrication and physical properties of permalloy nano-size wires

    International Nuclear Information System (INIS)

    Yu, C.; Lee, S.F.; Yao, Y.D.; Wong, M.S.; Huang, E.W.; Ma, Y.-R.; Tsai, J.L.; Chang, C.R.

    2003-01-01

    Nano-size NiFe wires with patterned shapes in half-ring-in-series, octagon-in-series, and zigzag-in-series configurations were fabricated. Their magnetoresistance was studied below room temperature and their magnetic domain images were investigated at room temperature by a magnetic force microscope. In general, we have experimentally demonstrated that the variation of the magnetoresistance of our patterned nano-size wires can be related to different domain configurations and explained by the domain switching effect. The number of magnetic domain walls in our patterned wires can be controlled by the shape anisotropy and the size of each section of patterns that form the wires

  16. Nano size crystals of goethite, α-FeOOH: Synthesis and thermal transformation

    International Nuclear Information System (INIS)

    Christensen, Axel Norlund; Jensen, Torben R.; Bahl, Christian R.H.; DiMasi, Elaine

    2007-01-01

    An aqueous suspension of amorphous iron(III) hydroxide was kept at room temperature (298 K) for 23 years. During this period of time the pH of the liquid phase changed from 4.3 to 2.85, and nano size crystals of goethite, α-FeOOH crystallised from the amorphous iron(III) hydroxide. Transmission electron microscopy (TEM) investigations, Moessbauer spectra, and powder X-ray diffraction using Co Kα radiation showed that the only iron containing crystalline phase present in the recovered product was α-FeOOH. The size of these nano particles range from 10 to 100 nm measured by TEM. The thermal decomposition of α-FeOOH was investigated by time-resolved in situ synchrotron radiation powder X-ray diffraction and the data showed that the sample of α-FeOOH transformed to α-Fe 2 O 3 in the temperature range 444-584 K. A quantitative phase analysis shows the increase in scattered X-ray intensity from α-Fe 2 O 3 to follow the decrease of intensity from α-FeOOH in agreement with the topotactic phase transition. - Graphical abstract: Nano size crystals of goethite, α-FeOOH formed from amorphous iron(III) hydroxide after 23 years, and transforms faster to α-Fe 2 O 3 upon heating

  17. Modification of unsaturated polyester resins using nano-size core ...

    African Journals Online (AJOL)

    Modification of unsaturated polyester resins using nano-size core-shell particles. MO Munyati, PA Lovell. Abstract. No Abstract Available Journal of Science and Technology Special Edition 2004: 24-31. Full Text: EMAIL FULL TEXT EMAIL FULL TEXT · DOWNLOAD FULL TEXT DOWNLOAD FULL TEXT.

  18. Nano sized clay detected on chalk particle surfaces

    DEFF Research Database (Denmark)

    Skovbjerg, Lone; Hassenkam, Tue; Makovicky, Emil

    2012-01-01

    that in calcite saturated water, both the polar and the nonpolar functional groups adhere to the nano sized clay particles but not to calcite. This is fundamentally important information for the development of conceptual and chemical models to explain wettability alterations in chalk reservoirs...

  19. Structural and Optical Properties of ZnO Thin Film Prepared by Oxidation of Zn Metal Powders

    International Nuclear Information System (INIS)

    Hassan, N.K.; Hashim, M.R.

    2013-01-01

    High quality ZnO nano structures have been fabricated at room temperature by a simple vacuum thermal evaporator from metallic Zn powders (99.999 % purity) on a silicon (100) substrate. The Zn thin films were then transferred into a thermal tube furnace for oxidation at 700 degree Celsius for different time durations. Time was found to be a critical factor in the synthesis. This was followed by characterization of their morphological, structural and optical properties. The morphology of the grown ZnO nano structures exhibited several large grains, which increased gradually with increasing oxidation time. The crystallinity of the grown nano structures was investigated using X-ray diffraction, revealing that the synthesized ZnO was in hexagonal wurtzite phase. The photoluminescence (PL) spectra of the fabricated ZnO nano structures showed high intensity peak in the UV region due to near-band-edge (NBE) emission in which the structures oxidized for 30 min showing highest intensity. (author)

  20. Modifications in Glass Ionomer Cements: Nano-Sized Fillers and Bioactive Nanoceramics

    Directory of Open Access Journals (Sweden)

    Shariq Najeeb

    2016-07-01

    Full Text Available Glass ionomer cements (GICs are being used for a wide range of applications in dentistry. In order to overcome the poor mechanical properties of glass ionomers, several modifications have been introduced to the conventional GICs. Nanotechnology involves the use of systems, modifications or materials the size of which is in the range of 1–100 nm. Nano-modification of conventional GICs and resin modified GICs (RMGICs can be achieved by incorporation of nano-sized fillers to RMGICs, reducing the size of the glass particles, and introducing nano-sized bioceramics to the glass powder. Studies suggest that the commercially available nano-filled RMGIC does not hold any significant advantage over conventional RMGICs as far as the mechanical and bonding properties are concerned. Conversely, incorporation of nano-sized apatite crystals not only increases the mechanical properties of conventional GICs, but also can enhance fluoride release and bioactivity. By increasing the crystallinity of the set matrix, apatites can make the set cement chemically more stable, insoluble, and improve the bond strength with tooth structure. Increased fluoride release can also reduce and arrest secondary caries. However, due to a lack of long-term clinical studies, the use of nano-modified glass ionomers is still limited in daily clinical dentistry. In addition to the in vitro and in vivo studies, more randomized clinical trials are required to justify the use of these promising materials. The aim of this paper is to review the modification performed in GIC-based materials to improve their physicochemical properties.

  1. Composition influence on positron annihilation parameters in ZnO-based nanocrystal semiconductor powders

    Energy Technology Data Exchange (ETDEWEB)

    Damonte, L.C.; Hernandez Fenollosa, M.A.; Donderis, V.; Mari, B. [Departamento de Fisica Aplicada, Universidad Politecnica de Valencia, Cami de Vera s/n, Valencia, 46071 (Spain)

    2007-07-01

    Zn{sub 1-x}Mg{sub x}O powders at various compositions were obtained by mechanical milling from the binary oxides. The progressive incorporation of Mg atoms into the ZnO lattice was monitored by X-ray diffraction (XRD). The evolution of annihilation parameters with milling time and composition were analyzed and related to the possible types of mechanical and substitutional induced defect present. It was concluded that the average lifetime constitute a useful parameter to sense the complete cation substitution in the wurtzite structure. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. Composition influence on positron annihilation parameters in ZnO-based nanocrystal semiconductor powders

    International Nuclear Information System (INIS)

    Damonte, L.C.; Hernandez Fenollosa, M.A.; Donderis, V.; Mari, B.

    2007-01-01

    Zn 1-x Mg x O powders at various compositions were obtained by mechanical milling from the binary oxides. The progressive incorporation of Mg atoms into the ZnO lattice was monitored by X-ray diffraction (XRD). The evolution of annihilation parameters with milling time and composition were analyzed and related to the possible types of mechanical and substitutional induced defect present. It was concluded that the average lifetime constitute a useful parameter to sense the complete cation substitution in the wurtzite structure. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  3. Nano-sized Adsorbate Structure Formation in Anisotropic Multilayer System

    Science.gov (United States)

    Kharchenko, Vasyl O.; Kharchenko, Dmitrii O.; Yanovsky, Vladimir V.

    2017-05-01

    In this article, we study dynamics of adsorbate island formation in a model plasma-condensate system numerically. We derive the generalized reaction-diffusion model for adsorptive multilayer system by taking into account anisotropy in transfer of adatoms between neighbor layers induced by electric field. It will be found that with an increase in the electric field strength, a structural transformation from nano-holes inside adsorbate matrix toward separated nano-sized adsorbate islands on a substrate is realized. Dynamics of adsorbate island sizes and corresponding distributions are analyzed in detail. This study provides an insight into details of self-organization of adatoms into nano-sized adsorbate islands in anisotropic multilayer plasma-condensate systems.

  4. High-pressure powder x-ray diffraction experiments on Zn at low temperature

    CERN Document Server

    Takemura, K; Fujihisa, H; Kikegawa, T

    2002-01-01

    High-pressure powder x-ray diffraction experiments have been performed on Zn with a He-pressure medium at low temperature. When the sample was compressed in the He medium at low temperature, large nonhydrostaticity developed, yielding erroneous lattice parameters. On the other hand, when the pressure was changed at high temperatures, good hydrostaticity was maintained. No anomaly in the volume dependence of the c/a axial ratio has been found.

  5. Influence of starting powder milling on magnetic properties of Mn-Zn ferrite

    Directory of Open Access Journals (Sweden)

    Miodrag M. Milutinov

    2017-06-01

    Full Text Available In this paper, the influence of additional sieving and milling of starting industrial Mn-Zn powders on magnetic properties was investigated. The starting powder was milled for 60 minutes, followed by sieving through 325 and 400 meshes. The starting and milled powders were used to fabricate toroid shaped samples sintered at 1200°C for 2 hours. Structural parameters of the fabricated samples were analysed by X-ray diffraction and scanning electron microscopy. Complex permeability, core loss density, and hysteresis were measured using the modified watt-meter method. The complex permeability and hysteresis loop were modelled with a new model proposed in the paper. The core loss density was modelled with the Steinmetz empirical equation. The experimental results and calculations show the significance of the additional milling and sieving process on magnetic properties of Mn-Zn ferrite in the frequency range 0.1-10MHz. These processes increase the relative permeability about 3 times and decrease the core loss 4 times by milling of the starting powder.

  6. Doped nanocrystalline ZnO powders for non-linear resistor applications by spray pyrolysis method.

    Science.gov (United States)

    Hembram, Kaliyan; Vijay, R; Rao, Y S; Rao, T N

    2009-07-01

    Homogeneous and doped nanocrystalline ZnO powders (30-200 nm) were synthesized by spray pyrolysis technique. The spray pyrolysed powders were calcined in the temperature range of 500-750 degrees C. Formation of insulating pyrochlore phase started from 700 degrees C during the calcination itself. The calcined powders were compacted and sintered at different temperatures ranging from 900-1200 degrees C for 0.5-4 h. The densification behavior was found to be dependent on calcination temperature of the nanopowder. The resulting discs were found to have density (5.34-5.62 g/cc) in the range of 96-99% of theoretical density. The breakdown voltage value obtained for the nanopowder based non-linear resistor is 10.3 kV/cm with low leakage current density of 0.7 microA/cm2 and coefficient of nonlinearity as high as 193. The activation energy for grain growth of the doped ZnO nanopowder powders is 449.4 +/- 15 kJ/mol.

  7. Sorption behavior of human bone powder towards 60 Co and 65 Zn

    International Nuclear Information System (INIS)

    Abdel-Fattah, A.T.; Essa, M.W.A.; Mohamed, S.A.; Molokhia, M.K.

    1990-01-01

    Human bone powder 30-40 Μ in diameter was prepared from human bone femurs as fat-free (FFB), protein-free (PFB) or left untreated as raw bone powder (RB). The sorption behavior of human bone powder towards 60 Co and 65 Zn was studied. The uptake changed with the type of bone powder to be : PFB>FFB>RB. The increase in the concentration of cobalt(from 10 -6 to 10 -1 Mole/litre)and of zinc (from 10 -7 to 10 -4 M/1) increased the uptake of 60 Co and 65 Zn. Freunclich-type isotherm was successfully applied on the uptake data of both ions and the slopes of these isotherms were, nearly, directly proportional to their uptake values. The uptake was found to be less influenced by the PH. In case of cobalt the uptake increased till PH 4, followed by a plateau till PH 8 while in case of zinc the PH effect is much less pronounced

  8. Comparative kinetic analysis of89 Sr,60 Co and65 Zn Uptake by human bone powder

    International Nuclear Information System (INIS)

    Abdel-Fatah, A.T.A.; Essa, M.W.A.; Mohamed, S.A.; Molokhia, M.K.

    1990-01-01

    Human bone powder samples were prepared from recent femurs. The Bone particles range between 30 and 40 MU in diameter. One portion of this powder was prepared fat-free (FFB), the second portion as protein-free (PFB) and the last portion was left as raw bone powder-(RB). The sequence of uptake of 89 Sr by these types of bone powder is : FFB > RB > PFB, while that of 60 Co and 65 Zn is: PFB > FFB > RB. Kinetic analysis of the uptake curves of the 3 isotopes indicated that these processes proceed in 3 distinct steps; very fast initial, moderate intermediate and slow last step. The obtained rates of uptake indicated that : (1) the uptake by PEB is faster in its third step than the other types, (2) the most predominant step in case of 89 Sr and 60 Co is the third step (ion exchange step) while in case of 65 Zn it is the first step (physical adsorption), (3) defatenisation or deproteinisation, in general, inhances the uptake process

  9. Dopants incorporation in ZnO mechanical milled powders sensed by positrons

    International Nuclear Information System (INIS)

    Damonte, L. C.; Donderis, V.; Hernandez Fenollosa, M. A.

    2007-01-01

    M-doped ZnO (M: Cd, Mg) powders obtained by mechanical milling were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM) and positron lifetime annihilation spectroscopy (PALS). The mixing of the oxides is followed by means of XRD and SEM. As milling proceeds, a clear reduction of grain size and homogenization are observed. The evolution of annihilation parameters with milling time and cation content were analyzed and related with the kind of mechanical induced defect involved. Ternary oxides Zn 1-x M x O were efficiency obtained for certain compositions. The results showed that positrons constitute a well suited probe to characterize the cation substitution in the ZnO oxide lattice.

  10. Dopants incorporation in ZnO mechanical milled powders sensed by positrons

    Energy Technology Data Exchange (ETDEWEB)

    Damonte, L. C., E-mail: damonte@fisica.unlp.edu.ar; Donderis, V.; Hernandez Fenollosa, M. A. [Universidad Politecnica de Valencia, Departamento de Fisica Aplicada (Spain)

    2007-09-15

    M-doped ZnO (M: Cd, Mg) powders obtained by mechanical milling were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM) and positron lifetime annihilation spectroscopy (PALS). The mixing of the oxides is followed by means of XRD and SEM. As milling proceeds, a clear reduction of grain size and homogenization are observed. The evolution of annihilation parameters with milling time and cation content were analyzed and related with the kind of mechanical induced defect involved. Ternary oxides Zn{sub 1-x}M{sub x}O were efficiency obtained for certain compositions. The results showed that positrons constitute a well suited probe to characterize the cation substitution in the ZnO oxide lattice.

  11. Preparation of TiO2 Nanocrystallite Powders Coated with 9 mol% ZnO for Cosmetic Applications in Sunscreens

    Directory of Open Access Journals (Sweden)

    Moo-Chin Wang

    2012-02-01

    Full Text Available The preparation of TiO2 nanocrystallite powders coated with and without 9 mol% ZnO has been studied for cosmetic applications in sunscreens by a co-precipitation process using TiCl4 and Zn(NO32·6H2O as starting materials. XRD results show that the phases of anatase TiO2 and rutile TiO2 coexist for precursor powders without added ZnO (T-0Z and calcined at 523 to 973 K for 2 h. When the T-0Z precursor powders are calcined at 1273 K for 2 h, only the rutile TiO2 appears. In addition, when the TiO2 precursor powders contain 9 mol% ZnO (T-9Z are calcined at 873 to 973 K for 2 h, the crystallized samples are composed of the major phase of rutile TiO2 and the minor phases of anatase TiO2 and Zn2Ti3O8. The analyses of UV/VIS/NIR spectra reveal that the absorption of the T-9Z precursor powders after being calcined has a red-shift effect in the UV range with increasing calcination temperature. Therefore, the TiO2 nanocrystallite powders coated with 9 mol% ZnO can be used as the attenuate agent in the UV-A region for cosmetic applications in sunscreens.

  12. In vitro toxicity test of nano-sized magnesium oxide synthesized via solid-phase transformation

    Science.gov (United States)

    Zheng, Jun; Zhou, Wei

    2018-04-01

    Nano-sized magnesium oxide (MgO) has been a promising potential material for biomedical pharmaceuticals. In the present investigation, MgO nanoparticles synthesized through in-situ solid-phase transformation based on the previous work (nano-Mg(OH)2 prepared by precipitation technique) using magnesium nitrate and sodium hydroxide. The phase structure and morphology of the MgO nanoparticles are characterized by X-ray powder diffraction (XRD), selected area electronic diffraction (SAED) and transmission electron microscopy (TEM) respectively. In vitro hemolysis tests are adopted to evaluate the toxicity of the synthesized nano-MgO. The results evident that nano-MgO with lower concentration is slightly hemolytic, and with concentration increasing nano-MgO exhibit dose-responsive hemolysis.

  13. Photocatalytic self-cleaning properties of cellulosic fibers modified by nano-sized zinc oxide

    Energy Technology Data Exchange (ETDEWEB)

    Moafi, Hadi Fallah; Shojaie, Abdollah Fallah, E-mail: a.f.shojaie@guilan.ac.ir; Zanjanchi, Mohammad Ali

    2011-03-31

    Nano-sized zinc oxide was synthesized and deposited onto cellulosic fibers using the sol-gel process at ambient temperature. The prepared materials were characterized using several techniques including scanning electron microscopy, transmission electron microscopy, diffuse reflectance spectroscopy, X-ray diffraction and thermogravimetric analysis. X-ray diffraction studies of the ZnO-coated fiber indicate formation of the hexagonal crystal phase which was satisfactory crystallized on the fiber surface. The electron micrographs show formation of zinc oxide nanoparticles within 10-15 nm in size which have been homogeneously dispersed on the fiber surface. The prepared materials show significant photocatalytic self-cleaning activity, which was monitored by diffuse reflectance spectroscopy. The photoactivity was studied upon measuring the photodegradation of methylene blue and eosin yellowish under UV-Vis irradiation. The photocatalytic activity of the treated fabrics was fully maintained performing several cycles of photodegradation.

  14. Photocatalytic self-cleaning properties of cellulosic fibers modified by nano-sized zinc oxide

    International Nuclear Information System (INIS)

    Moafi, Hadi Fallah; Shojaie, Abdollah Fallah; Zanjanchi, Mohammad Ali

    2011-01-01

    Nano-sized zinc oxide was synthesized and deposited onto cellulosic fibers using the sol-gel process at ambient temperature. The prepared materials were characterized using several techniques including scanning electron microscopy, transmission electron microscopy, diffuse reflectance spectroscopy, X-ray diffraction and thermogravimetric analysis. X-ray diffraction studies of the ZnO-coated fiber indicate formation of the hexagonal crystal phase which was satisfactory crystallized on the fiber surface. The electron micrographs show formation of zinc oxide nanoparticles within 10-15 nm in size which have been homogeneously dispersed on the fiber surface. The prepared materials show significant photocatalytic self-cleaning activity, which was monitored by diffuse reflectance spectroscopy. The photoactivity was studied upon measuring the photodegradation of methylene blue and eosin yellowish under UV-Vis irradiation. The photocatalytic activity of the treated fabrics was fully maintained performing several cycles of photodegradation.

  15. Synthesis and Characterization of Nano-Sized Hexagonal and Spherical Nanoparticles of Zinc Oxide

    Directory of Open Access Journals (Sweden)

    M. A. Moghri Moazzen

    2012-09-01

    Full Text Available ZnO plays an important role in many semiconductors technological aspects.  Here,  direct  precipitation  method  was  employed  for  the synthesis of nano-sized hexagonal ZnO particles, which is based on chemical  reactions between  raw materials used  in  the  experiment. ZnO  nanoparticles  were  synthesized  by  calcinations  of  the  ZnO precursor precipitates  at 250  ˚C  for 3hours. The particle  size  and structure of the products have been confirmed by XRD. The FT-IR study  confirms  the  presence  of  functional  groups.  Also,  the morphology  and  size  distribution  of  ZnO  nanoparticles  was analyzed by TEM images. The optical properties were investigated by UV–Visible  spectroscopy. The XRD  results  show  that  the  size of  the prepared nanoparticles  is  in  the  range  of 20–40 nm, which this value  is  in good agreement with  the TEM  results. The FT-IR spectrum clearly indicates the formation of an interfacial chemical bond between Zn and O. Also  the UV absorption depends on  the particles  size  and morphology,  so  the  optical properties  enhances with  decreasing  nanoparticles  size.  Moreover  the  direct precipitation technique is a feasible method for production of ZnO nanopowders.

  16. Luminescence of one dimensional ZnO, GeO{sub 2}–Zn{sub 2}GeO{sub 4} nanostructure through thermal evaporation of Zn and Ge powder mixture

    Energy Technology Data Exchange (ETDEWEB)

    Pham, Vuong-Hung, E-mail: vuong.phamhung@hust.edu.vn; Kien, Vu Trung; Tam, Phuong Dinh; Huy, Pham Thanh

    2016-07-15

    Graphical abstract: - Highlights: • ZnO and GeO{sub 2}–ZnGeO{sub 4} nanowires were fabricated by thermal evaporation of Zn and Ge powder mixture. • Morphology of specimens were observed to have a nanowire structure to rod-like morphology. • Strong NBE emission band with suppressed visible green emission band were observed on the dominant ZnO nanowires. • Strong emission of ∼530 nm were observed on the GeO{sub 2}–Zn{sub 2}GeO{sub 4} nanowires. - Abstract: This paper reports the first attempt for fabrication of thermal evaporated Zn–Ge powder mixture to achieve near-band-edge (NBE) emission of ZnO and visible emission of GeO{sub 2}–Zn{sub 2}GeO{sub 4} nanowires with controllable intensities. The nanowires were fabricated by thermal evaporation of Zn and Ge powder mixture, particularly, by using different Zn:Ge ratio, temperature and evaporated times. The morphology of nanowires was depended on the Zn and Ge ratio that was observed to have a nanowire structure to rod-like morphology. The thermal evaporation of Zn:Ge powder mixture resulted in formation of dominant ZnO or GeO{sub 2}–Zn{sub 2}GeO{sub 4} nanowires as a function of evaporated parameters. These results suggest that the application of thermal evaporation of Zn and Ge mixture for potential application in synthesis of ZnO or GeO{sub 2}–Zn{sub 2}GeO{sub 4} nanowires for optoelectronic field.

  17. Ductility and work hardening in nano-sized metallic glasses

    Energy Technology Data Exchange (ETDEWEB)

    Chen, D. Z., E-mail: dzchen@caltech.edu [Division of Engineering and Applied Sciences, California Institute of Technology, Pasadena, California 91125 (United States); Gu, X. W. [Department of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125 (United States); An, Q.; Goddard, W. A. [Materials and Process Simulation Center, California Institute of Technology, Pasadena, California 91125 (United States); Greer, J. R. [Division of Engineering and Applied Sciences, California Institute of Technology, Pasadena, California 91125 (United States); The Kavli Nanoscience Institute, California Institute of Technology, Pasadena, California 91125 (United States)

    2015-02-09

    In-situ nano-tensile experiments on 70 nm-diameter free-standing electroplated NiP metallic glass nanostructures reveal tensile true strains of ∼18%, an amount comparable to compositionally identical 100 nm-diameter focused ion beam samples and ∼3 times greater than 100 nm-diameter electroplated samples. Simultaneous in-situ observations and stress-strain data during post-elastic deformation reveal necking and work hardening, features uncharacteristic for metallic glasses. The evolution of free volume within molecular dynamics-simulated samples suggests a free surface-mediated relaxation mechanism in nano-sized metallic glasses.

  18. Morphology, Structure and Nonstoichiometry of ZnCr2O4 Nanophased Powder

    Directory of Open Access Journals (Sweden)

    O. Milosevic

    2003-10-01

    Full Text Available It is well established that gas/humidity-sensing properties of spinels are markedly influenced by their stoichiometry and microstructure. In this work nucleation and spinel phase development in the Zn-Cr-O system were investigated from the viewpoint of structural and morphological phenomena occurred during nanophased particle synthesis through aerosol reaction. The aerosol was generated from nitrates precursor solution using ultrasonic atomizer operated at 1.7 MHz. The influence of different decomposition schedules on the particle chemical content and morphology was determined by adjusting the processing parameters (aerosol droplet density 3.9x106 droplets/cm3, droplet velocity 0.035m/s, max. temperature 900oC and residence times 3, 6 and 9s. A composite particle structure comprised of primary crystallites sized from 22 to 44nm is revealed by SEM and TEM analysis. XRD structural analysis (crystallite size, microstrains, unit cell and ionic occupancies is performed in accordance with procedure based on Koalariet-Xfit program. A certain degree of non-stochiometry is characteristic for all powders. Homogenous distribution of the constituting elements and Zn/Cr ratio of about 0.68 are proved by EDAX mapping analysis in 470nm sized as-prepared particles. After additional treatment at 1000oC octahedral crystals form with the (111 surface dominat. Evaluated spinel non-stochiometry (Zn/Cr=0.58 is a result of the ZnO dissolving (1.9%wt in the stoichiometric ZnCr2O4. Determination of the way by which the ZnO is incorporated into the spinel lattice is performed according to the procedure based on calculation of both formation and attachment energies.

  19. Core-shell architectures as nano-size transporters

    International Nuclear Information System (INIS)

    Adeli, M.; Zarnegar, Z.; Kabiri, R.; Salimi, F.; Dadkah, A.

    2006-01-01

    Core-shell architectures containing poly (ethylene imine) (PEI) as a core and poly (lactide) (PLA) as arms were prepared. PEI was used as macro initiator for ring opening polymerization of lactide. PEI-PLA core-shell architectures were able to encapsulate guest molecules. Size of the core-shell architectures was between 10- 100 nm, hence they can be considered as nano carriers to transport the guest molecules. Transport capacity of nano carriers depends on their nano-environments and type of self-assembly in solvent. In solid state nano carriers self-assemble as long structures with nano-size diameter or they form network structures. Aggregations type depends on the concentration of nano carriers in solution. Effect of the shell thickness and aggregation type on the release rate are also investigated

  20. Magnetic, hyperthermic and structural properties of zn substituted CaFe2O4 powders

    Science.gov (United States)

    Kheradmand, Abbas; Vahidi, Omid; Masoudpanah, S. M.

    2018-03-01

    In the present study, we have synthesized single phase Ca1 - x Zn x Fe2O4 powders by hydrothermal method. The cation distribution between the tetrahedral and octahedral sites in the spinel structure and the magnetic properties as a function of the zinc substitution have been investigated by X-ray diffraction (XRD), infrared spectroscopy and vibrating sample magnetometer methods. The obtained XRD pattern indicated that the synthesized particles had single phase cubic spinel structure with no impurity. The magnetic measurements showed that the saturation magnetization increased from 83 to 98 emu/g with the addition of zinc due to the decrease of inversity. The particle size observed by electron microscopy decreased from 1.38 to 0.97 µm with the increase of zinc addition. The Ca0.7Zn0.3Fe2O4 powders exhibited appropriate heating capability for hyperthermia applications with the maximum AC heating temperature of 20 °C and specific loss power of 9.29 W/g.

  1. Nano size crystals of goethite, α-FeOOH: Synthesis and thermal transformation

    Science.gov (United States)

    Christensen, Axel Nørlund; Jensen, Torben R.; Bahl, Christian R. H.; DiMasi, Elaine

    2007-04-01

    An aqueous suspension of amorphous iron(III) hydroxide was kept at room temperature (298 K) for 23 years. During this period of time the pH of the liquid phase changed from 4.3 to 2.85, and nano size crystals of goethite, α-FeOOH crystallised from the amorphous iron(III) hydroxide. Transmission electron microscopy (TEM) investigations, Mössbauer spectra, and powder X-ray diffraction using Co K α radiation showed that the only iron containing crystalline phase present in the recovered product was α-FeOOH. The size of these nano particles range from 10 to 100 nm measured by TEM. The thermal decomposition of α-FeOOH was investigated by time-resolved in situ synchrotron radiation powder X-ray diffraction and the data showed that the sample of α-FeOOH transformed to α-Fe 2O 3 in the temperature range 444-584 K. A quantitative phase analysis shows the increase in scattered X-ray intensity from α-Fe 2O 3 to follow the decrease of intensity from α-FeOOH in agreement with the topotactic phase transition.

  2. Nano Size Crystals of Geothite, alpha-FeOOH: Synthesis and Thermal Transformation

    Energy Technology Data Exchange (ETDEWEB)

    Christensen,A.; Jensen, T.; Bahl, C.; DiMasi, E.

    2007-01-01

    An aqueous suspension of amorphous iron(III) hydroxide was kept at room temperature (298 K) for 23 years. During this period of time the pH of the liquid phase changed from 4.3 to 2.85, and nano size crystals of goethite, {alpha}-FeOOH crystallized from the amorphous iron(III) hydroxide. Transmission electron microscopy (TEM) investigations, Moessbauer spectra, and powder X-ray diffraction using Co K{alpha} radiation showed that the only iron containing crystalline phase present in the recovered product was {alpha}-FeOOH. The size of these nano particles range from 10 to 100 nm measured by TEM. The thermal decomposition of {alpha}-FeOOH was investigated by time-resolved in situ synchrotron radiation powder X-ray diffraction and the data showed that the sample of {alpha}-FeOOH transformed to {alpha}-Fe{sub 2}O{sub 3} in the temperature range 444--584 K. A quantitative phase analysis shows the increase in scattered X-ray intensity from {alpha}-Fe{sub 2}O{sub 3} to follow the decrease of intensity from {alpha}-FeOOH in agreement with the topotactic phase transition.

  3. Photoluminescent nano-sized ternary and quaternary complexes of thorium(IV)

    International Nuclear Information System (INIS)

    Baranwal, B.P.; Jain, A.K.; Varma, A.; Singh, A.K.; Fatma, T.

    2011-01-01

    Some ternary and quaternary complexes of thorium(IV) with the general formula [Th(OOCCH 3 ) 2-n (SB) n (OOCC 15 H 31 ) 2 ] (HSB=Schiff bases and n=1 or 2) have been synthesized by the stepwise substitutions of acetate ions from thorium(IV) acetate, first with straight chain carboxylic acid and then with Schiff bases. The complexes are characterized by elemental analyses, spectral (electronic, infrared, 1 H NMR, FAB mass, photoluminescence and powder XRD) and TEM studies. Conductance measurements indicated non-conducting behaviour of the complexes. Structural parameters from powder XRD data for complexes 5 and 6 which indicate poorly crystalline nano-sized triclinic particles. Electronic absorption spectra of the complexes showed π → π * and n → π * charge transfer transitions. All complexes displayed fluorescence and a correlation was sought between luminescence spectra of complexes in solution at room temperature. On the basis of physico-chemical studies, coordination number 8 was assigned for thorium(IV) in the complexes. The morphology and microstructure of the complexes were examined with transmission electron microscopy (TEM) and the selected area electron diffraction (SAED). (orig.)

  4. Microstructure and properties of SA 106B carbon steel after treatment of the melt with nano-sized TiC particles

    International Nuclear Information System (INIS)

    Park, Jin-Ju; Hong, Sung-Mo; Park, Eun-Kwang; Kim, Kyeong-Yeol; Lee, Min-Ku; Rhee, Chang-Kyu

    2014-01-01

    Carbon steel dispersed with nano-sized TiC ceramic particles was fabricated using the liquid metal casting process by means of their ex-situ introduction. For this purpose, the nano-sized TiC powders with an initial average size of 40 nm were first mechanically activated with two metal powders (Fe, Ni) and then introduced externally into the molten carbon steel during the casting process. According to the chemical composition analysis, 90% of the initial TiC nanoparticles were discovered within the cast carbon steel. Compared to cast carbon steel without TiC nanoparticles, the grain size refinement and mechanical property enhancement were achieved. Atom probe tomographic analysis revealed that the TiC nanoparticles were approximately 30 nm in size in the carbon steel matrix with a number density of 1.49×10 21 m −3

  5. Ductility Enhancement of Molybdenum Phase by Nano-sized Oxide Dispersions

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Bruce

    2008-07-18

    The objective of this research is to understand and to remedy the impurity effects for room-temperature ductility enhancement of molybdenum (Mo) based alloys by the inclusion of nano-sized metal oxide dispersions. This research combines theoretical, computational, and experimental efforts. The results will help to formulate systematic strategies in searching for better composed Mo-based alloys with optimal mechanical properties. For this project, majority of the research effort was directed to atomistic modeling to identify the mechanisms responsible for the oxygen embrittling and ductility enhancement based on fundamental electronic structure analysis. Through first principles molecular dynamics simulations, it was found that the embrittling impurity species were attracted to the metal oxide interface, consistent with previous experiments. Further investigation on the electronic structures reveals that the presence of embrittling species degrades the quality of the metallic chemical bonds in the hosting matrix in a number of ways, the latter providing the source of ductility. For example, the spatial flexibility of the bonds is reduced, and localization of the impurity states occurs to pin the dislocation flow. Rice’s criterion has been invoked to explain the connections of electronic structure and mechanical properties. It was also found that when impurity species become attracted to the metal oxide interface, some of the detrimental effects are alleviated, thus explaining the observed ductility enhancement effects. These understandings help to develop predictive capabilities to facilitate the design and optimization of Mo and other high temperature alloys (e.g. ODS alloys) for fossil energy materials applications. Based on the theoretical and computational studies, the experimental work includes the preparation of Mo powders mixed with candidate nano-sized metal oxides, which were then vacuum hot-pressed to make the Mo alloys. Several powder mixing methods

  6. Characteristics of Sodium Polyacrylate/Nano-Sized Carbon Hydrogel for Biomedical Patch.

    Science.gov (United States)

    Park, Jong-Kyu; Seo, Sun-Kyo; Cho, Seungkwan; Kim, Han-Sung; Lee, Chi-Hwan

    2018-03-01

    Conductive hydrogels were prepared for biomedical patch in order to improve the electrical conductivity. Sodium polyacrylate and nano-sized carbon were mixed and fabricated by aqueous solution gelation process in various contents of nano-sized carbon with 0.1, 0.5, 1.0 and 2.0 wt%. Sodium polyacrylate/nano-sized carbon conductive hydrogels were investigated by molecular structure, surface morphology and electrical conductivity. The conductivity of the hydrogel/nano-sized carbon conductive hydrogel proved to be 10% higher than conductive hydrogel without nano-sized carbon. However, it was founded that conductive hydrogels with nano-sized carbon content from 0.5 up to 2.0 wt% were remarkably decreased. This may be due to the non-uniform distribution of nano-sized carbon, resulting from agglomerates of nano-sized carbon. The developed hydrogel is intended for use in the medical and cosmetic fields that is applicable to supply micro-current from device to human body.

  7. Preparation of tetrapod-like ZnO/TiO{sub 2} core-shell nanostructures as photocatalytic powder

    Energy Technology Data Exchange (ETDEWEB)

    Sartori, A.; Visentin, F.; De Zorzi, C.; Natali, M.; Gerbasi, R.; Rossetto, G. [ICIS-DPM-CNR, Padova (Italy); El Habra, N. [ICIS-DPM-CNR, Padova (Italy); Dipartimento di Scienze Chimiche, Padova (Italy); Garoli, D. [Dipartimento di Fisica, Padova (Italy); LANN, Padova (Italy); Casarin, M. [Dipartimento di Scienze Chimiche, Padova (Italy)

    2011-08-15

    The coupling of zinc oxide tetrapods (t-ZnO) with anatase TiO{sub 2} in the form of CVD coatings on ZnO nanotetrapods was investigated. t-ZnO/TiO{sub 2} core-shell structures, consisting of uniformly and completely TiO{sub 2} covered ZnO nanotetrapods, were characterized by scanning electron microscopy, X-ray diffraction and UV-Vis spectra. Photocatalytic activity, determined by degradation of a sodium methyl red solution, was found to be comparable to pure t-ZnO, while improved separation easiness was verified that makes the presented powders promising for wastewater treatment. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  8. Room temperature ferromagnetism in Eu-doped ZnO nanoparticulate powders prepared by combustion reaction method

    International Nuclear Information System (INIS)

    Franco, A.; Pessoni, H.V.S.; Soares, M.P.

    2014-01-01

    Nanoparticulate powders of Eu-doped ZnO with 1.0, 1.5, 2.0 and 3.0 at% Eu were synthesized by combustion reaction method using zinc nitrate, europium nitrate and urea as fuel without subsequent heat treatments. X-ray diffraction patterns (XRD) of all samples showed broad peaks consistent with the ZnO wurtzite structure. The absence of extra reflections in the diffraction patterns ensures the phase purity, except for x=0.03 that exhibits small reflection corresponding to Eu 2 O 3 phase. The average crystallite size determined from the most prominent (1 0 1) peak of the diffraction using Scherrer's equation was in good agreement with those determined by transmission electron microscopy (TEM); being ∼26 nm. The magnetic properties measurements were performed using a vibrating sample magnetometer (VSM) in magnetic fields up to 2.0 kOe at room temperature. The hysteresis loops, typical of magnetic behaviors, indicating that the presence of an ordered magnetic structure can exist in the Eu-doped ZnO wurtzite structure at room temperature. The room temperature ferromagnetism behavior increases with the Eu 3+ doping concentration. All samples exhibited the same Curie temperature (T C ) around ∼726 K, except for x=0.01; T C ∼643 K. High resolution transmission electron microscopy (HRTEM) images revealed defects/strain in the lattice and grain boundaries of Eu-doped ZnO nanoparticulate powders. The origin of room temperature ferromagnetism in Eu-doped ZnO nanoparticulate powders was discussed in terms of these defects, which increase with the Eu 3+ doping concentration. - Highlights: • Room-temperature ferromagnetism. • Structural and magnetic properties of nanoparticulate powders of Zn 1−x Eu x O. • Combustion reaction method

  9. Nano-sized calcium phosphate particles for periodontal gene therapy.

    Science.gov (United States)

    Elangovan, Satheesh; Jain, Shardool; Tsai, Pei-Chin; Margolis, Henry C; Amiji, Mansoor

    2013-01-01

    Growth factors such as platelet-derived growth factor (PDGF) have significantly enhanced periodontal therapy outcomes with a high degree of variability, mostly due to the lack of continual supply for a required period of time. One method to overcome this barrier is gene therapy. The aim of this in vitro study is to evaluate PDGF-B gene delivery in fibroblasts using nano-sized calcium phosphate particles (NCaPP) as vectors. NCaPP incorporating green fluorescent protein (NCaPP-GFP) and PDGF-B (NCaPP-PDGF-B) plasmids were synthesized using an established precipitation system and characterized using transmission electron microscopy and 1.2% agarose gel electrophoresis. Biocompatibility and transfection of the nanoplexes in fibroblasts were evaluated using cytotoxicity assay and florescence microscopy, respectively. Polymerase chain reaction and enzyme-linked immunosorbent assay were performed to evaluate PDGF-B transfection after different time points of treatments, and the functionality of PDGF-B transfection was evaluated using the cell proliferation assay. Synthesized NCaPP nanoplexes incorporating the genes of GFP and PDGF-B were spherical in shape and measured about 30 to 50 nm in diameter. Gel electrophoresis confirmed DNA incorporation and stability within the nanoplexes, and 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium reagent assay demonstrated their biocompatibility in fibroblasts. In vitro transfection studies revealed a higher and longer lasting transfection after NCaPP-PDGF-B treatment, which lasted up to 96 hours. Significantly enhanced fibroblast proliferation observed in NCaPP-PDGF-B-treated cells confirmed the functionality of these nanoplexes. NCaPP demonstrated higher levels of biocompatibility and efficiently transfected PDGF plasmids into fibroblasts under described in vitro conditions.

  10. Hydrothermal synthesis and electrochemical properties of nano-sized Co-Sn alloy anodes for lithium ion batteries

    International Nuclear Information System (INIS)

    He Jianchao; Zhao Hailei; Wang Jing; Wang Jie; Chen Jingbo

    2010-01-01

    Research highlights: → Nano-sized Co-Sn alloys were synthesized by hydrothermal route. → Li 2 O and CoSn can buffer the large volume change associated with lithiation of Sn. → A two-step reaction mechanism of CoSn 2 alloy during cycling was confirmed. - Abstract: Nano-sized Co-Sn alloys with a certain amount of Sn oxides used as potential anode materials for lithium ion batteries were synthesized by hydrothermal route. The effects of hydrothermal conditions and post annealing on the phase compositions and the electrochemical properties of synthesized powders were characterized by means of X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) with energy dispersive spectra (EDS) analysis and galvanostatic cycling tests. Prolonging the dwelling time at the same hydrothermal temperature can increase the content of Sn oxides, which will lead to a high initial irreversible capacity loss but a better cycling stability owing to the buffer effect of irreversible product Li 2 O. Heat-treatment can increase the crystallinity and cause the presence of a certain amount of inert CoSn component, which both have positive impact on the cycling stability of Co-Sn electrode. By comparison with the lithiation/delithiation processes of metal Sn, a two-step mechanism of CoSn 2 alloy during cycling was confirmed.

  11. Novel polyoxometalate silica nano-sized spheres: efficient catalysts for olefin oxidation and the deep desulfurization process.

    Science.gov (United States)

    Nogueira, Lucie S; Ribeiro, Susana; Granadeiro, Carlos M; Pereira, Eulália; Feio, Gabriel; Cunha-Silva, Luís; Balula, Salete S

    2014-07-07

    A novel method to prepare silica nano-sized particles incorporating polyoxometalates was developed leading to a new efficient heterogeneous oxidative catalyst. Zinc-substituted polyoxotungstate [PW11Zn(H2O)O39](5-) (PW11Zn) was encapsulated into silica nanoparticles using a cross-linked organic-inorganic core, performed through successive spontaneous reactions in water. The potassium salt of PW11Zn and the composite formed, PW11Zn-APTES@SiO2, were characterized by a myriad of solid-state methods such as FT-IR, FT-Raman, (31)P and (13)C CP/MAS solid-state NMR, elemental analysis and SEM-EDS, confirming the integrity of the PW11Zn structure immobilized in the silica nanoparticles. The new composite has shown to be a versatile catalyst for the oxidation of olefins and also to catalyze the desulfurization of a model oil using H2O2 as the oxidant and acetonitrile as the solvent. The novel composite material was capable of being recycled without significant loss of activity and maintaining its structural stability for consecutive desulfurization and olefin oxidative cycles.

  12. Maple leaf (Acer sp.) extract mediated green process for the functionalization of ZnO powders with silver nanoparticles.

    Science.gov (United States)

    Vivekanandhan, Singaravelu; Schreiber, Makoto; Mason, Cynthia; Mohanty, Amar Kumar; Misra, Manjusri

    2014-01-01

    The functionalization of ZnO powders with silver nanoparticles (AgNPs) through a novel maple leaf extract mediated biological process was demonstrated. Maple leaf extract was found to be a very effective bioreduction agent for the reduction of silver ions. The reduction rate of Ag(+) into Ag(0) was found to be much faster than other previously reported bioreduction rates and was comparable to the reduction rates obtained through chemical means. The functionalization of ZnO particles with silver nanoparticles through maple leaf extract mediated bioreduction of silver was investigated through UV-visible spectrophotometry, transmission electron microscopy (TEM), and X-ray diffraction analysis. It was found that the ZnO particles were coated with silver nanoparticles 5-20 nm in diameter. The photocatalytic ability of the ZnO particles functionalized with silver nanoparticles was found to be significantly improved compared to the photocatalytic ability of the neat ZnO particles. The silver functionalized ZnO particles reached 90% degradation of the dye an hour before the neat ZnO particles. Copyright © 2013 Elsevier B.V. All rights reserved.

  13. Synthesis and characterization of hexagonal nano-sized nickel selenide by simple hydrothermal method assisted by CTAB

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-07-01

    Nano-sized nickel selenide powders have been successfully synthesized via an improved hydrothermal route based on the reaction between NiCl{sub 2}.6H{sub 2}O, SeCl{sub 4} and hydrazine (N{sub 2}H{sub 4}.H{sub 2}O) in water, in present of cetyltrimethyl ammonium bromide (CTAB) as surfactant, at various conditions. The products were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and X-ray energy dispersive spectroscopy analysis. Effects of temperature, reaction time and reductant agent on the morphology, the particle sizes and the phase of the final products have been investigated. It was found that the phase and morphology of the products could be greatly influenced by these parameters. The synthesis procedure is simple and uses less toxic reagents than the previously reported methods. Photoluminescence (PL) was used to study the optical properties of NiSe samples.

  14. Kinetics of physico-chemical processes during intensive mechanical processing of ZnO-MnO{sub 2} powder mixture

    Energy Technology Data Exchange (ETDEWEB)

    Kakazey, M.; Vlasova, M.; Dominguez-Patino, M. [CIICAp-Universidad Autonoma del Estado de Morelos, Cuernavaca (Mexico); Juarez-Arellano, E.A., E-mail: eajuarez@unpa.edu.mx [Universidad del Papaloapan, Tuxtepec, Oaxaca (Mexico); Bykov, A. [Institute for Problems of Materials Science of NASU, Kyiv (Ukraine); Leon, I. [CIQ-Universidad Autonoma del Estado de Morelos, Cuernavaca (Mexico); Siqueiros-Diaz, A. [FCQI-Universidad Autonoma del Estado de Morelos, Cuernavaca (Mexico)

    2011-10-15

    Experimental results of electron paramagnetic resonance spectra, X-ray diffraction, scanning electron microscopy and infrared spectroscopy demonstrate that the kinetic of the physical and chemical processes that takes place during prolonged intensive mechanical processing (MP, 03120min) of powder mixtures of 50%wt ZnO+50%wt MnO{sub 2} can be described as a three stage process. (1) 030min, particles destruction, formation of superficial defects, fast increment of sample average temperature (from 290 to {approx}600K) and annealing of defects with the lowest energy of activation E{sub ac}. (2) 30390min, further particle destruction, slow increment of sample average temperature (from {approx}600 to {approx}700K), formation and growth of a very disordered layer of {beta}-MnO{sub 2} around ZnO particles, dehydration of MnO{sub 2}, formation of solid solution of Mn{sup 2+} ions in ZnO, formation of nano-quasiamorphous states in the ZnO-MnO{sub 2} mixture and onset of the formation of the ZnMnO{sub 3} phase. (3) 3903120min, the sample average temperature remains constant ({approx}700K), the reaction is completed and the spinel ZnMnO{sub 3} phase with a unit cell a=8.431(1) A and space group Fd3-barm is the only phase present in the sample. No ferromagnetism at room temperature was detected in this study. - Highlights: > The kinetics during mechanical processing of ZnO-MnO{sub 2} samples is a three stage process. > First stage, reduction of crystallites size and accumulation of defects. > Second stage, nano-quasiamorphous states formation and onset of the ZnMnO{sub 3} phase. > Third stage, complete reaction to the spinel ZnMnO{sub 3} phase.

  15. Kinetics of physico-chemical processes during intensive mechanical processing of ZnO-MnO2 powder mixture

    International Nuclear Information System (INIS)

    Kakazey, M.; Vlasova, M.; Dominguez-Patino, M.; Juarez-Arellano, E.A.; Bykov, A.; Leon, I.; Siqueiros-Diaz, A.

    2011-01-01

    Experimental results of electron paramagnetic resonance spectra, X-ray diffraction, scanning electron microscopy and infrared spectroscopy demonstrate that the kinetic of the physical and chemical processes that takes place during prolonged intensive mechanical processing (MP, 0 MP >3120min) of powder mixtures of 50%wt ZnO+50%wt MnO 2 can be described as a three stage process. (1) 0 MP >30min, particles destruction, formation of superficial defects, fast increment of sample average temperature (from 290 to ∼600K) and annealing of defects with the lowest energy of activation E ac . (2) 30 MP >390min, further particle destruction, slow increment of sample average temperature (from ∼600 to ∼700K), formation and growth of a very disordered layer of β-MnO 2 around ZnO particles, dehydration of MnO 2 , formation of solid solution of Mn 2+ ions in ZnO, formation of nano-quasiamorphous states in the ZnO-MnO 2 mixture and onset of the formation of the ZnMnO 3 phase. (3) 390 MP >3120min, the sample average temperature remains constant (∼700K), the reaction is completed and the spinel ZnMnO 3 phase with a unit cell a=8.431(1) A and space group Fd3-barm is the only phase present in the sample. No ferromagnetism at room temperature was detected in this study. - Highlights: → The kinetics during mechanical processing of ZnO-MnO 2 samples is a three stage process. → First stage, reduction of crystallites size and accumulation of defects. → Second stage, nano-quasiamorphous states formation and onset of the ZnMnO 3 phase. → Third stage, complete reaction to the spinel ZnMnO 3 phase.

  16. A Mössbauer and magnetic study of ball milled Fe-doped ZnO Powders

    Energy Technology Data Exchange (ETDEWEB)

    Zamora, Ligia E., E-mail: ligia.zamora@correounivalle.edu.co; Paz, J. C.; Piamba, J. F.; Tabares, J. A.; Alcázar, G. A. Pérez [Universidad del Valle, Departamento de física (Colombia)

    2015-06-15

    The structural and magnetic properties of Fe-doped ZnO are reported in this study, as obtained by mechanical alloying from elemental powders of ZnO and Fe. The properties of Zn{sub 0.90}Fe{sub 0.10}O samples alloying while varying the milling time (6, 12, 24 and 36 h) are also reported. The Rietveld refinement of X-ray Diffraction (XRD) patterns revealed that the system presents two structures: the würtzite structure of ZnO and the bcc structure of α-Fe. The Mössbauer spectra show that the samples present three components: a ferromagnetic component, associated with the Fe phase and two paramagnetic components, associated with the Fe atoms, which penetrate inside the ZnO matrix behaving as Fe{sup 3+} and Fe{sup 2+}. The milling time contributes to an increase in the paramagnetic sites, and a solubility limit of the Fe atoms in the ZnO lattice was detected. The VSM measurements at room temperature detected ferromagnetic behavior with a saturation magnetization of 11 emu/g and a coercive field of 330 Oe for the sample alloyed over 24 h. A similar behavior was shown by the other samples.

  17. Enhanced electrochemical performance of nano-sized LiFePO4/C synthesized by an ultrasonic-assisted co-precipitation method

    International Nuclear Information System (INIS)

    Liu Youyong; Cao Chuanbao

    2010-01-01

    A simple and effective method, the ultrasonic-assisted co-precipitation method, was employed to synthesize nano-sized LiFePO 4 /C. A glucose solution was used as the carbon source to produce in situ carbon to improve the conductivity of LiFePO 4 . Ultrasonic irradiation was adopted to control the size and homogenize the LiFePO 4 /C particles. The sample was characterized by X-ray powder diffraction, field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM). FE-SEM and TEM show that the as-prepared sample has a reduced particle size with a uniform size distribution, which is around 50 nm. A uniform amorphous carbon layer with a thickness of about 4-6 nm on the particle surface was observed, as shown in the HRTEM image. The electrochemical performance was demonstrated by the charge-discharge test and electrochemical impedance spectra measurements. The results indicate that the nano-sized LiFePO 4 /C presents enhanced discharge capacities (159, 147 and 135 mAh g -1 at 0.1, 0.5 and 2 C-rate, respectively) and stable cycling performance. This study offers a simple method to design and synthesis nano-sized cathode materials for lithium-ion batteries.

  18. Development and characterization of Al-Zn alloy by ingot metallurgy and powder metallurgy with improved mechanical properties

    International Nuclear Information System (INIS)

    Waseem, M.; Awais, H.B.; Zauha, M.S.; Tariq, N.H.

    2007-01-01

    Current project focuses on the production of AI-Zn alloy AA7075 used for wide range of applications like Aircraft components, missile and other structural applications. The above alloy was developed by two different routes. One was melting /casting, after which alloy was characterized by microstructural - examination (optical and SEM) and mechanical testing. Other route was the preparation of this alloy by powder metallurgy. This involves preparation of powders, mechanical alloying, compaction, sintering, rolling, solution treatment and aging then analysis. Powders of Aluminum, Zinc and powders of master alloys of AI-Cu, AI-Mg, AI-Mn, and AI-Cr were Mechanical alloyed. Then this powder was compacted by uniaxial press to form pellets. Sintering was carried out at 500 degree C and then hot rolled in Ar atmosphere. After solution and aging treatments samples were characterized. It is observed that there is about 12-21% improvement in mechanical properties such as tensile strength, yield strength, ductility and fracture toughness due to the more fine microstructure and less segregation than ingot metallurgy route. (author)

  19. Synthesis of Si, N co-Doped Nano-Sized TiO2 with High Thermal Stability and Photocatalytic Activity by Mechanochemical Method

    Directory of Open Access Journals (Sweden)

    Peisan Wang

    2018-05-01

    Full Text Available Τhe photocatalytic activity in the range of visible light wavelengths and the thermal stability of the structure were significantly enhanced in Si, N co-doped nano-sized TiO2, and synthesized through high-energy mechanical milling of TiO2 and SiO2 powders, which was followed by calcination at 600 °C in an ammonia atmosphere. High-energy mechanical milling had a pronounced effect on the mixing and the reaction between the starting powders and greatly favored the transformation of the resultant powder mixture into an amorphous phase that contained a large number of evenly-dispersed nanocrystalline TiO2 particles as anatase seeds. The experimental results suggest that the elements were homogeneously dispersed at an atomic level in this amorphous phase. After calcination, most of the amorphous phase was crystallized, which resulted in a unique nano-sized crystalline-core/disordered-shell morphology. This novel experimental process is simple, template-free, and provides features of high reproducibility in large-scale industrial production.

  20. Preparation of Cu2ZnSnS4 nano-crystalline powder by mechano-chemical method

    Science.gov (United States)

    Alirezazadeh, Farzaneh; Sheibani, Saeed; Rashchi, Fereshteh

    2018-01-01

    Copper zinc tin sulfide (Cu2ZnSnS4, CZTS) is one of the most promising ceramic materials as an absorber layer in solar cells due to its suitable band gap, high absorption coefficient and non-toxic and environmental friendly constituent elements. In this work, nano-crystalline CZTS powder was synthesized by mechanical milling. Elemental powders of Cu, Zn, Sn and were mixed in atomic ratio of 2:1:1:4 according to the stoichiometry of Cu2ZnSnS4 and then milled in a planetary high energy ball mill under argon atmosphere. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and diffusion reflectance spectroscopy (DRS). XRD results confirm the formation of single-phase CZTS with kesterite structure after 20 h of milling. Also, the mean crystallite size was about 35 nm. SEM results show that after 20 h of milling, the product has a relatively uniform particle size distribution. Optical properties of the product indicate that the band gap of prepared CZTS is 1.6 eV which is near to the optimum value for photovoltaic solar cells showing as a light absorber material in solar energy applications.

  1. Improved compaction of ZnO nano-powder triggered by the presence of acetate and its effect on sintering.

    Science.gov (United States)

    Dargatz, Benjamin; Gonzalez-Julian, Jesus; Guillon, Olivier

    2015-04-01

    The retention of nanocrystallinity in dense ceramic materials is still a challenge, even with the application of external pressure during sintering. The compaction behavior of high purity and acetate enriched zinc oxide (ZnO) nano-powders was investigated. It was found that acetate in combination with water plays a key role during the compaction into green bodies at moderate temperatures. Application of constant pressure resulted in a homogeneous green body with superior packing density (86% of theoretical value) at moderate temperature (85 °C) in the presence of water. In contrast, no improvement in density could be achieved if pure ZnO powder was used. This compaction behavior offers superior packing of the particles, resulting in a high relative density of the consolidated compact with negligible coarsening. Dissolution accompanying creep diffusion based matter transport is suggested to strongly support reorientation of ZnO particles towards densities beyond the theoretical limit for packing of ideal monosized spheres. Finally, the sintering trajectory reveals that grain growth is retarded compared to conventional processing up to 90% of theoretical density. Moreover, nearly no radial shrinkage was observed after sinter-forging for bodies performed with this advanced processing method.

  2. Compressive Deformation Behavior of Open-Cell Cu-Zn-Al Alloy Foam Made Through P/M Route Using Mechanically Alloyed Powder

    Science.gov (United States)

    Barnwal, Ajay Kumar; Mondal, D. P.; Kumar, Rajeev; Prasanth, N.; Dasgupta, R.

    2018-03-01

    Cu-Zn-Al foams of varying porosity fractions using mechanical alloyed powder have been made through powder metallurgy route. Here, NH4 (HCO3) was used as a space holder. Mechanically alloyed Cu-Zn-Al is made using a planetary ball mill taking the ratio of Cu/Zn/Al = 70:25:5 (by weight ratio). The ball/powder ratios were varied in the four ranges 10:1, 15:1, 20:1, and 25:1. Green compacts of milled powder and space holder samples were sintered at three stages at three different temperatures 350, 550, and 850 °C for 1 h at each stage. The crystalline size and particle size as a function of ball/powder ratios were examined. The compressive deformation responses of foams are varied with relative density and the ball/powder ratio. The plateau stress and energy absorption of these foams increase with an increase in relative density but decreases with increase in ball/powder ratio, even though crystalline size decreases. This has further been explained on the basis of particle morphology as a function of ball/powder ratio.

  3. Chemoselective Oxidation of Bio-Glycerol with Nano-Sized Metal Catalysts

    DEFF Research Database (Denmark)

    Li, Hu; Kotni, Ramakrishna; Zhang, Qiuyun

    2015-01-01

    to selectively oxidize glycerol and yield products with good selectivity is the use of nano-sized metal particles as heterogeneous catalysts. In this short review, recent developments in chemoselective oxidation of glycerol to specific products over nano-sized metal catalysts are described. Attention is drawn...... to various reaction parameters such as the type of the support, the size of the metal particles, and the acid/base properties of the reaction medium which were illustrated to largely influence the activity of the nanocatalyst and selectivity to the target product. - See more at: http...

  4. Zn2+ in-situ substitution behavior during the formation of BaTiO3 coatings from plasma-sprayed powders collected in liquid nitrogen

    Science.gov (United States)

    Liu, Zhe; Xing, Zhiguo; Wang, Haidou; Xue, Zifan; Chen, Shuying; Cui, Xiufang; Jin, Guo

    2018-04-01

    The dielectric performance of BaTiO3 ceramic coatings is enhanced significantly by the addition of ZnO. In this study, the maximum relative permittivity value (εr ≈ 923) was measured in BaTiO3 coatings with ZnO added at 6 wt%. The Curie temperature (Tc) was in the range of 111 °C-121 °C for all of the ZnO-modified BaTiO3 coatings. Tc shifted to low temperatures as the ZnO content increased. Detailed analyses were performed to determine the phase composition and optical band gaps of powders collected in liquid nitrogen, which showed that the Zn2+ ions were incorporated into the BaTiO3 lattice where they substituted into the Ti4+ sites, and the composite powders (BaTiO3 + 6 wt% ZnO) tolerated high temperatures in the plasma beam. In addition, some residual Zn accumulated in the grain boundary in the form of ZnO. X-ray diffraction and Raman spectroscopy showed that the substitution led to changes in the compositional and structural properties. The red shift in the optical band gap of BaTiO3 indicated that the ZnTi'' defects caused by the dopants acted as carriers in the doped BaTiO3 coatings.

  5. Synthesis and characterization of nano-sized CaCO3 in purified diet

    Science.gov (United States)

    Mulyaningsih, N. N.; Tresnasari, D. R.; Ramahwati, M. R.; Juwono, A. L.; Soejoko, D. S.; Astuti, D. A.

    2017-07-01

    The growth and development of animals depend strongly on the balanced nutrition in the diet. This research aims is to characterize the weight variations of nano-sized calcium carbonate (CaCO3) in purified diet that to be fed to animal model of rat. The nano-sized CaCO3 was prepared by milling the calcium carbonate particles for 20 hours at a rotation speed of 1000 rpm and resulting particle size in a range of 2-50 nm. Nano-sized CaCO3 added to purified diet to the four formulas that were identified as normal diet (N), deficiency calcium (DC), rich in calcium (RC), and poor calcium (PC) with containing in nano-sized CaCO3 much as 0.50 %, 0.00 %, 0.75 % and 0.25 % respectively. The nutritional content of the purified diet was proximate analyzed, it resulted as followed moisture, ash, fat, protein, crude fiber. The quantities of chemical element were analyzed by atomic absorption spectrometry (AAS), it resulted iron, magnesium, potassium and calcium. The results showed that N diet (Ca: 16,914.29 ppm) were suggested for healthy rats and RC diet (Ca: 33,696.13 ppm) for conditioned osteoporosis rats. The crystalline phases of the samples that were examined by X-ray diffraction showed that crystalline phase increased with the increasing concentration of CaCO3.

  6. Nano-sized polystyrene affects feeding, behavior and physiology of brine shrimp Artemia franciscana larvae

    NARCIS (Netherlands)

    Bergami, Elisa; Bocci, Elena; Vannuccini, Maria Luisa; Monopoli, Marco; Salvati, Anna; Dawson, Kenneth A; Corsi, Ilaria

    Nano-sized polymers as polystyrene (PS) constitute one of the main challenges for marine ecosystems, since they can distribute along the whole water column affecting planktonic species and consequently disrupting the energy flow of marine ecosystems. Nowadays very little knowledge is available on

  7. Elaboration and Characterization of Nano-Sized AlxMoyOz/Al Thermites

    National Research Council Canada - National Science Library

    Comet, M; Spitzer, D

    2006-01-01

    ...) has been developed at the Institut franco-allemand de recherches de Saint Louis (ISL). This process consists of a new sol-gel method nano-sized mixed AlxMoyOz phases whose structure is correlated to the chemical composition...

  8. TRANSPORT AND DEPOSITION OF NANO-SIZE PARTICLES IN THE UPPER HUMAN RESPIRATORY AIRWAYS

    Science.gov (United States)

    TRANSPORT AND DEPOSITION OF NANO-SIZE PARTICLES IN THE UPPER HUMAN RESPIRATORY AIRWAYS. Zhe Zhang*, Huawei Shi, Clement Kleinstreuer, Department of Mechanical and Aerospace Engineering, North Carolina State University, Raleigh, NC 27695-7910; Chong S. Kim, National Health and En...

  9. Thermal Stress Behavior of Micro- and Nano-Size Aluminum Films

    International Nuclear Information System (INIS)

    Hanabusa, T.; Kusaka, K.; Nishida, M.

    2008-01-01

    In-situ observation of thermal stresses in thin films deposited on silicon substrate was made by X-ray and synchrotron radiation. Specimens prepared in this experiment were micro- and nano-size thin aluminum films with and without passivation film. The thickness of the film was 1 micrometer for micro-size films and 10, 20 and 50 nanometer for nano-size films. The stress measurement in micro-size films was made by X-ray radiation whereas the measurement of nano-size films was made by synchrotron radiation. Residual stress measurement revealed tensile stresses in all as-deposited films. Thermal stresses were measured in a series of heating- and cooling-stage. Thermal stress behavior of micro-size films revealed hysteresis loop during a heating and cooling process. The width of a hysteresis loop was larger in passivated film that unpassivated film. No hysteresis loops were observed in nano-size films with SiO 2 passivation. Strengthning mechanism in thin films was discussed on a passivation film and a film thickness

  10. A simple route for renewable nano-sized arjunolic and asiatic acids and self-assembly of arjuna-bromolactone

    Directory of Open Access Journals (Sweden)

    2008-07-01

    Full Text Available While separating two natural nano-sized triterpenic acids via bromolactonization, we serendipitously discovered that arjuna-bromolactone is an excellent gelator of various organic solvents. A simple and efficient method for the separation of two triterpenic acids and the gelation ability and solid state 1D-helical self-assembly of nano-sized arjuna-bromolactone are reported.

  11. The result of synthesis analysis of the powder TiO{sub 2}/ZnO as a layer of electrodes for dye sensitized solar cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Retnaningsih, Lilis, E-mail: lilisretna@gmail.com; Muliani, Lia [Research Center for Electronics and Telecommunications Indonesian Institute of Sciences (PPET-LIPI) Kampus LIPI, Jl. Sangkuriang, Bandung 40135 (Indonesia)

    2016-04-19

    This study has been conducted synthesis of TiO{sub 2} nanoparticle powders and ZnO nanoparticle powder into a paste to be in this research, dye-sensitive solar cells (DSSC) was produced by TiO{sub 2} nanopowder and ZnO nanopowder synthesis to make paste that is applied as electrode. This electrode works based on photon absorbed by dye and transferred to different composition of TiO{sub 2}/ ZnO particle. Properties of DSSC are affected by fabrication method, parameter and dimension of TiO{sub 2} / ZnO nanoparticles, technique and composition of TiO{sub 2} / ZnO paste preparation is important to get the higher performance of DSSC. Doctor blade is a method for electrode coating on glass substrate. The electrode was immersed into dye solution of Z907 and ethanol. From the experiment, the effect of TiO{sub 2} and ZnO nanopowder mixture for electrode was investigated. XRD characterization show anatase and rutile phase, which sintered TiO{sub 2}/ZnO has intensity more than 11,000. SEM characterization shows the composition of 20% TiO{sub 2} / 80% ZnO has better porosity. Higher efficiency that is investigated by I-V measurement using Sun Simulator.

  12. Gum Tragacanth-Mediated Synthesis of Nanocrystalline ZnO Powder for Use in Varistors

    Science.gov (United States)

    Liu, Ting-Ting; Wang, Mao-Hua; Su, Hang; Chen, Xi; Chen, Chao; Zhang, Ruo-Chen

    2015-10-01

    Zinc oxide nanopowders were synthesized by a sol-gel method with gum tragacanth and zinc nitrate as raw materials. Gum tragacanth was used as stabilizer to control the mobility of zinc cations and the growth of the nanopowders. Thermo-gravimetric analysis, x-ray diffraction, Fourier-transform infrared spectroscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, and scanning electron microscopy were used to characterize the as-prepared samples. Zinc oxide (ZnO) nanoparticles calcined at different temperatures had a hexagonal wurtzite structure with average particle size ranging from 32.29 nm to 42.83 nm. The crystallinity of ZnO nanoparticles was improved by increasing the calcination temperature. The density of ZnO varistor ceramics sintered at 1150°C for 2 h in air was 5.46 g/cm3, which was 97.5% of the theoretical density, their breakdown voltage was 4572 V/cm, and their nonlinear coefficient was ~16.8. This method can be used as an excellent alternative method for synthesis of ZnO nanoparticles with a plant extract as a raw material. Our experimental results show our method had the advantage of improving the electrical performance of ZnO varistors.

  13. Corrosion behavior and protective ability of Zn and Zn-Co electrodeposits with embedded polymeric nanoparticles

    International Nuclear Information System (INIS)

    Boshkov, N.; Tsvetkova, N.; Petrov, P.; Koleva, D.; Petrov, K.; Avdeev, G.; Tsvetanov, Ch.; Raichevsky, G.; Raicheff, R.

    2008-01-01

    The anodic behavior, corrosion resistance and protective ability of Zn and alloyed Zn-Co (∼3 wt.%) nanocomposite coatings were investigated in a model corrosion medium of 5% NaCl solution. The metallic matrix of the layers incorporates core-shell nano-sized stabilized polymeric micelles (SPMs) obtained from poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) block co-polymers. The protective properties of the composite coatings were evaluated using potentiodynamic polarization technique, polarization resistance measurements and powder X-ray diffraction. The sizes and distribution of the stabilized polymeric micelles in the starting electrolytes used as well as in the metal matrices of the layers were investigated using scanning and transmission electron microscopy. The results obtained are compared to those of electrodeposited Zn and Zn-Co (∼3 wt.%) alloy coatings at identical conditions and demonstrate the enhanced protective characteristics of the Zn nanocomposites during the investigating period. The influence of the SPMs on the corrosion resistance of the nanocomposite layers is commented and discussed

  14. A coprecipitation technique to prepare ZnNb2O6 powders

    Indian Academy of Sciences (India)

    Unknown

    Ammonium hydroxide was used to precipitate Zn2+ and Nb5+ cations as hydro- xides simultaneously. This precursor on ... tion technique from simple water soluble inorganic salts. This process can avoid complex steps such as ... dispersed in amyl acetate on a carbon coated TEM copper grid. 3. Results and discussion.

  15. Densification and volumetric change during supersolidus liquid phase sintering of prealloyed brass Cu28Zn powder: Modeling and optimization

    Directory of Open Access Journals (Sweden)

    Mohammadzadeh A.

    2014-01-01

    Full Text Available An investigation has been made to use response surface methodology and central composite rotatable design for modeling and optimizing the effect of sintering variables on densification of prealloyed Cu28Zn brass powder during supersolidus liquid phase sintering. The mathematical equations were derived to predict sintered density, densification parameter, porosity percentage and volumetric change of samples using second order regression analysis. As well as the adequacy of models was evaluated by analysis of variance technique at 95% confidence level. Finally, the influence and interaction of sintering variables, on achieving any desired properties was demonstrated graphically in contour and three dimensional plots. In order to better analyze the samples, microstructure evaluation was carried out. It was concluded that response surface methodology based on central composite rotatable design, is an economical way to obtain arbitrary information with performing the fewest number of experiments in a short period of time.

  16. Nano-sized structured layered positive electrode materials to enable high energy density and high rate capability lithium batteries

    Science.gov (United States)

    Deng, Haixia; Belharouak, Ilias; Amine, Khalil

    2012-10-02

    Nano-sized structured dense and spherical layered positive active materials provide high energy density and high rate capability electrodes in lithium-ion batteries. Such materials are spherical second particles made from agglomerated primary particles that are Li.sub.1+.alpha.(Ni.sub.xCo.sub.yMn.sub.z).sub.1-tM.sub.tO.sub.2-dR.sub.d- , where M is selected from can be Al, Mg, Fe, Cu, Zn, Cr, Ag, Ca, Na, K, In, Ga, Ge, V, Mo, Nb, Si, Ti, Zr, or a mixture of any two or more thereof, R is selected from F, Cl, Br, I, H, S, N, or a mixture of any two or more thereof, and 0.ltoreq..alpha..ltoreq.0.50; 0

  17. Spheroidization of glass powders for glass ionomer cements.

    Science.gov (United States)

    Gu, Y W; Yap, A U J; Cheang, P; Kumar, R

    2004-08-01

    Commercial angular glass powders were spheroidized using both the flame spraying and inductively coupled radio frequency plasma spraying techniques. Spherical powders with different particle size distributions were obtained after spheroidization. The effects of spherical glass powders on the mechanical properties of glass ionomer cements (GICs) were investigated. Results showed that the particle size distribution of the glass powders had a significant influence on the mechanical properties of GICs. Powders with a bimodal particle size distribution ensured a high packing density of glass ionomer cements, giving relatively high mechanical properties of GICs. GICs prepared by flame-spheroidized powders showed low strength values due to the loss of fine particles during flame spraying, leading to a low packing density and few metal ions reacting with polyacrylic acid to form cross-linking. GICs prepared by the nano-sized powders showed low strength because of the low bulk density of the nano-sized powders and hence low powder/liquid ratio of GICs.

  18. NANO-SIZED PIGMENT APPLICATIONS IN İZNİK TILES

    Directory of Open Access Journals (Sweden)

    Esin GÜNAY

    2012-12-01

    Full Text Available Traditional İznik tiles are known as “unproducable” due to its high quartz content. İznik tiles contain four different layers as “body, engobe (slip, decors and glaze” and each one has some different starting materials. Recent studies have showed that the production techniques and the particle size of pigments are important parameters in development of colours. TUBITAK MRC and İznik Foundation carried out an experimental work to improve and understand the effects of nanotechnology application to İznik tiles. High quartz content was kept as it is and pigments were applied in decorationas nano-sized pigments.İznik tiles were produced and comparison was carried out between traditional and modern İznik tiles in colour and brightness. Characterization techniques were used in order to understand andcompare the results and also the effects of nano-sized pigments to İznik tiles.

  19. Application of rapid solidification powder metallurgy to the fabrication of high-strength, high-ductility Mg-Al-Zn-Ca-La alloy through hot extrusion

    Energy Technology Data Exchange (ETDEWEB)

    Ayman, Elsayed, E-mail: ayman@jwri.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Junko, Umeda; Katsuyoshi, Kondoh [Joining and Welding Research Institute, Osaka University, 11-1 Mihogaoka, Ibaraki, Osaka 567-0047 (Japan)

    2011-01-15

    The microstructure and mechanical properties of hot extruded Mg-7Al-1Zn-1Ca powder alloys with an addition of 1.5% La or 3.3% La were investigated. Both rapidly solidified powders, produced via spinning water atomization process, and cast billets were extruded at 573, 623 and 673 K to optimize the processing conditions for obtaining better mechanical response. Powders were consolidated using both cold compaction and spark plasma sintering. The tensile properties of the extruded alloys were then evaluated and correlated to their microstructures. The results showed that the use of rapidly solidified Mg-7Al-1Zn-1Ca alloy powders with La additions could lead to effective grain refinement and super saturation of alloying elements, which in turn resulted in the improved mechanical response. The Mg-7Al-1Zn-1Ca-1.5La alloy extruded at 573 K attained ultimate tensile strength of 450 {+-} xx MPa and elongation of 17 {+-} xx%, superior to the Mg-7Al-1Zn-1Ca-3.3La alloy and other Mg alloys like Mg-Al-Mn-Ca. This may help extend the application of Mg alloys to higher load-carrying parts while maintaining the excellent advantage of light weight.

  20. Targeted Therapy for Acute Autoimmune Myocarditis with Nano-Sized Liposomal FK506 in Rats.

    Directory of Open Access Journals (Sweden)

    Keiji Okuda

    Full Text Available Immunosuppressive agents are used for the treatment of immune-mediated myocarditis; however, the need to develop a more effective therapeutic approach remains. Nano-sized liposomes may accumulate in and selectively deliver drugs to an inflammatory lesion with enhanced vascular permeability. The aims of this study were to investigate the distribution of liposomal FK506, an immunosuppressive drug encapsulated within liposomes, and the drug's effects on cardiac function in a rat experimental autoimmune myocarditis (EAM model. We prepared polyethylene glycol-modified liposomal FK506 (mean diameter: 109.5 ± 4.4 nm. We induced EAM by immunization with porcine myosin and assessed the tissue distribution of the nano-sized beads and liposomal FK506 in this model. After liposomal or free FK506 was administered on days 14 and 17 after immunization, the cytokine expression in the rat hearts along with the histological findings and hemodynamic parameters were determined on day 21. Ex vivo fluorescent imaging revealed that intravenously administered fluorescent-labeled nano-sized beads had accumulated in myocarditic but not normal hearts on day 14 after immunization and thereafter. Compared to the administration of free FK506, FK506 levels were increased in both the plasma and hearts of EAM rats when liposomal FK506 was administered. The administration of liposomal FK506 markedly suppressed the expression of cytokines, such as interferon-γ and tumor necrosis factor-α, and reduced inflammation and fibrosis in the myocardium on day 21 compared to free FK506. The administration of liposomal FK506 also markedly ameliorated cardiac dysfunction on day 21 compared to free FK506. Nano-sized liposomes may be a promising drug delivery system for targeting myocarditic hearts with cardioprotective agents.

  1. Targeted Therapy for Acute Autoimmune Myocarditis with Nano-Sized Liposomal FK506 in Rats.

    Science.gov (United States)

    Okuda, Keiji; Fu, Hai Ying; Matsuzaki, Takashi; Araki, Ryo; Tsuchida, Shota; Thanikachalam, Punniyakoti V; Fukuta, Tatsuya; Asai, Tomohiro; Yamato, Masaki; Sanada, Shoji; Asanuma, Hiroshi; Asano, Yoshihiro; Asakura, Masanori; Hanawa, Haruo; Hao, Hiroyuki; Oku, Naoto; Takashima, Seiji; Kitakaze, Masafumi; Sakata, Yasushi; Minamino, Tetsuo

    2016-01-01

    Immunosuppressive agents are used for the treatment of immune-mediated myocarditis; however, the need to develop a more effective therapeutic approach remains. Nano-sized liposomes may accumulate in and selectively deliver drugs to an inflammatory lesion with enhanced vascular permeability. The aims of this study were to investigate the distribution of liposomal FK506, an immunosuppressive drug encapsulated within liposomes, and the drug's effects on cardiac function in a rat experimental autoimmune myocarditis (EAM) model. We prepared polyethylene glycol-modified liposomal FK506 (mean diameter: 109.5 ± 4.4 nm). We induced EAM by immunization with porcine myosin and assessed the tissue distribution of the nano-sized beads and liposomal FK506 in this model. After liposomal or free FK506 was administered on days 14 and 17 after immunization, the cytokine expression in the rat hearts along with the histological findings and hemodynamic parameters were determined on day 21. Ex vivo fluorescent imaging revealed that intravenously administered fluorescent-labeled nano-sized beads had accumulated in myocarditic but not normal hearts on day 14 after immunization and thereafter. Compared to the administration of free FK506, FK506 levels were increased in both the plasma and hearts of EAM rats when liposomal FK506 was administered. The administration of liposomal FK506 markedly suppressed the expression of cytokines, such as interferon-γ and tumor necrosis factor-α, and reduced inflammation and fibrosis in the myocardium on day 21 compared to free FK506. The administration of liposomal FK506 also markedly ameliorated cardiac dysfunction on day 21 compared to free FK506. Nano-sized liposomes may be a promising drug delivery system for targeting myocarditic hearts with cardioprotective agents.

  2. Kinetic model for transformation from nano-sized amorphous $TiO_2$ to anatase

    OpenAIRE

    Madras, Giridhar; McCoy, Benjamin J

    2006-01-01

    We propose a kinetic model for the transformation of nano-sized amorphous $TiO_2$ to anatase with associated coarsening by coalescence. Based on population balance (distribution kinetics) equations for the size distributions, the model applies a first-order rate expression for transformation combined with Smoluchowski coalescence for the coarsening particles. Size distribution moments (number and mass of particles) lead to dynamic expressions for extent of reaction and average anatase particl...

  3. Nano-sized polystyrene affects feeding, behavior and physiology of brine shrimp Artemia franciscana larvae.

    Science.gov (United States)

    Bergami, Elisa; Bocci, Elena; Vannuccini, Maria Luisa; Monopoli, Marco; Salvati, Anna; Dawson, Kenneth A; Corsi, Ilaria

    2016-01-01

    Nano-sized polymers as polystyrene (PS) constitute one of the main challenges for marine ecosystems, since they can distribute along the whole water column affecting planktonic species and consequently disrupting the energy flow of marine ecosystems. Nowadays very little knowledge is available on the impact of nano-sized plastics on marine organisms. Therefore, the present study aims to evaluate the effects of 40nm anionic carboxylated (PS-COOH) and 50nm cationic amino (PS-NH2) polystyrene nanoparticles (PS NPs) on brine shrimp Artemia franciscana larvae. No signs of mortality were observed at 48h of exposure for both PS NPs at naplius stage but several sub-lethal effects were evident. PS-COOH (5-100μg/ml) resulted massively sequestered inside the gut lumen of larvae (48h) probably limiting food intake. Some of them were lately excreted as fecal pellets but not a full release was observed. Likewise, PS-NH2 (5-100µg/ml) accumulated in larvae (48h) but also adsorbed at the surface of sensorial antennules and appendages probably hampering larvae motility. In addition, larvae exposed to PS-NH2 undergo multiple molting events during 48h of exposure compared to controls. The activation of a defense mechanism based on a physiological process able to release toxic cationic NPs (PS-NH2) from the body can be hypothesized. The general observed accumulation of PS NPs within the gut during the 48h of exposure indicates a continuous bioavailability of nano-sized PS for planktonic species as well as a potential transfer along the trophic web. Therefore, nano-sized PS might be able to impair food uptake (feeding), behavior (motility) and physiology (multiple molting) of brine shrimp larvae with consequences not only at organism and population level but on the overall ecosystem based on the key role of zooplankton on marine food webs. Copyright © 2015 Elsevier Inc. All rights reserved.

  4. Fabrication and properties of high-strength extruded brass using elemental mixture of Cu-40% Zn alloy powder and Mg particle

    Energy Technology Data Exchange (ETDEWEB)

    Atsumi, Haruhiko, E-mail: atsumi-h@jwri.osaka-u.ac.jp [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Imai, Hisashi; Li, Shufeng; Kondoh, Katsuyoshi [Joining and Welding Research Institute, Osaka University, 11-1 Mihogaoka, Ibaraki, Osaka 567-0047 (Japan); Kousaka, Yoshiharu; Kojima, Akimichi [San-etsu Metals Co. Ltd., 1892 Ohta, Tonami, Toyama 939-1315 (Japan)

    2012-08-15

    In this paper, high-strength brass (Cu-40% Zn) alloy with magnesium (Mg) element was fabricated via powder technology process, and the effect of the additive Mg element on microstructural and mechanical properties of extruded brass alloys with {alpha}-{beta} duplex phases was investigated. Pre-mixed Cu-40% Zn alloy powder with 0.5-1.5 mass% pure Mg powder (Cu-40% Zn + Mg) was consolidated using a spark plasma sintering (SPS) equipment. SPSed Cu-40% Zn + Mg specimens consisted of {alpha}-{beta} duplex phases containing Mg(Cu{sub 1-x}Zn{sub x}){sub 2} intermetallic compounds (IMCs) with a mean particle size of 10-30 {mu}m in diameter. The IMCs were completely dissolved in the {alpha}-{beta} duplex phases by a heat-treatment at 973 K for 15 min; thus, in order to disperse fine IMCs on {alpha}-{beta} duplex phase matrix, the SPSed Cu-40% Zn + Mg specimens were pre-heated at the solid solutionizing condition, and immediately extruded. The extruded specimen exhibited fine {alpha}-{beta} duplex phases, containing very fine precipitates of the above Mg(Cu{sub 1-x}Zn{sub x}){sub 2} IMCs with 0.5-3.0 {mu}m in diameter. In particular, a mean grain size of the extruded Cu-40% Zn + 1.0% Mg specimen was 3.32 {mu}m analyzed using an electron back-scattered diffraction. Tensile properties of the extruded Cu-40% Zn + 1.0% Mg specimen were an average value of yield strength (YS): 328 MPa, ultimate tensile strength (UTS): 553 MPa, and 25% elongation. This indicated that the extruded Cu-40% Zn + 1.0% Mg specimen revealed the significantly high-strength properties compared to a conventional binary brass alloy with 229 MPa YS and 464 MPa UTS. A high strengthening mechanism of this wrought brass alloy was mainly due to the grain refinement because of a pinning effect by the fine Mg(Cu{sub 1-x}Zn{sub x}){sub 2} precipitates at the boundaries of each phase. -- Highlights: Black-Right-Pointing-Pointer New high-strength extruded brass alloy with Mg was fabricated via powder metallurgy. Black

  5. Nano-sized precipitation and properties of a low carbon niobium micro-alloyed bainitic steel

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Z.J. [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Department of Materials Science and Engineering, McMaster University, Hamilton L8S 4L8 (Canada); Ma, X.P. [Department of Materials Science and Engineering, McMaster University, Hamilton L8S 4L8 (Canada); Shang, C.J., E-mail: cjshang@ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Wang, X.M. [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Subramanian, S.V. [Department of Materials Science and Engineering, McMaster University, Hamilton L8S 4L8 (Canada)

    2015-08-12

    The present work focuses on microstructure evolution and precipitation strengthening during tempering at region of 550–680 °C to elucidate the structure–property relationship in the steel. The effect of tempering on the development of a 700 MPa grade high strength hot rolled cost-effective bainitic steel was studied for infrastructure applications. Granular bainite with dispersed martenisit–austenite (M–A) constituents in the bainitic ferrite matrix was obtained after hot rolling and air cooling to room temperature. The decomposition of M–A constituents to cementite carbides and the precipitation of nano-sized NbC carbides in bainitic matrix on tempering were characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Nano-sized precipitates of NbC precipitated during tempering were in average diameter of ~4.1–6.1 nm. There were ~86–173 MPa increases in yield strength after tempering at region of 550–680 °C. It is noticeable that those nano-sized NbC precipitates provide an effective way to significantly increase the strength of the low carbon bainitic steel. High yield strength of 716 MPa with high ductility (uniform elongation of 9.3% and total elongation of 22.4%), low yield to tensile ratio of 0.9 and good low temperature toughness of 47 J (half thickness) at –40 °C was obtained after tempering at 680 °C for 30 min.

  6. Characteristic of Water Pervaporation Using Hydrophilic Composite Membrane Containing Functional Nano Sized NaA zeolites

    International Nuclear Information System (INIS)

    Oh, Duckkyu; Lee, Yongtaek

    2013-01-01

    The NaA zeolite particles were dispersed in a poly(vinyl alcohol) (PVA) matrix to prepare a composite membrane. The nano sized zeolite particles of NaA were synthesized in the laboratory and the mean size was approximately 60 nm. Pervaporation characteristics such as a permeation flux and a separation factor were investigated using the membrane as a function of the feed concentration from 0.01 to 0.05 mole fraction and the weight % of NaA particles between 0 wt% and 5 wt% in the membrane. Also, the micro sized particles of 5 mm were dispersed in the membrane for a comparison purpose. When the ethanol concentration in the feed solution was 0.01 mole fraction, the flux of water significantly increased from 600 g/m 2 /hr to 2000 g/m 2 /hr as the content of the nano NaA particles in the membrane increased from 0 wt% to 5 wt%, while the NaA particles improved the separation factor from 1.5 to 7.9. When the flux of water through the membrane containing nano sized particles was roughly 15% increased compared to the micro sized particles, whereas the separation factor of water was found to be approximately 5% increased. It can be said that the role of the nano sized NaA particles is quite important since both the flux and the separation factor are strongly affected

  7. Grain Refinement and Mechanical Properties of Cu-Cr-Zr Alloys with Different Nano-Sized TiCp Addition.

    Science.gov (United States)

    Zhang, Dongdong; Bai, Fang; Wang, Yong; Wang, Jinguo; Wang, Wenquan

    2017-08-08

    The TiC p /Cu master alloy was prepared via thermal explosion reaction. Afterwards, the nano-sized TiC p /Cu master alloy was dispersed by electromagnetic stirring casting into the melting Cu-Cr-Zr alloys to fabricate the nano-sized TiC p -reinforced Cu-Cr-Zr composites. Results show that nano-sized TiC p can effectively refine the grain size of Cu-Cr-Zr alloys. The morphologies of grain in Cu-Cr-Zr composites changed from dendritic grain to equiaxed crystal because of the addition and dispersion of nano-sized TiC p . The grain size decreased from 82 to 28 μm with the nano-sized TiC p content. Compared with Cu-Cr-Zr alloys, the ultimate compressive strength (σ UCS ) and yield strength (σ 0.2 ) of 4 wt% TiC p -reinforced Cu-Cr-Zr composites increased by 6.7% and 9.4%, respectively. The wear resistance of the nano-sized TiCp-reinforced Cu-Cr-Zr composites increased with the increasing nano-sized TiCp content. The wear loss of the nano-sized TiC p -reinforced Cu-Cr-Zr composites decreased with the increasing TiC p content under abrasive particles. The eletrical conductivity of Cu-Cr-Zr alloys, 2% and 4% nano-sized TiCp-reinforced Cu-Cr-Zr composites are 64.71% IACS, 56.77% IACS and 52.93% IACS, respectively.

  8. A submerged ceramic membrane reactor for the p-nitrophenol hydrogenation over nano-sized nickel catalysts.

    Science.gov (United States)

    Chen, R Z; Sun, H L; Xing, W H; Jin, W Q; Xu, N P

    2009-02-01

    The catalytic hydrogenation of p-nitrophenol to p-aminophenol over nano-sized nickel catalysts was carried out in a submerged ceramic membrane reactor. It has been demonstrated that the submerged ceramic membrane reactor is more suitable for the p-nitrophenol hydrogenation over nano-sized nickel catalysts compared with the side-stream ceramic membrane reactor, and the membrane module configuration has a great influence on the reaction rate of p-nitrophenol hydrogenation and the membrane treating capacity. The deactivation of nano-sized nickel is mainly caused by the adsorption of impurity on the surface of nickel and the increase of oxidation degree of nickel.

  9. Recovery of yttrium from fluorescent powder of cathode ray tube, CRT: Zn removal by sulphide precipitation

    International Nuclear Information System (INIS)

    Innocenzi, Valentina; De Michelis, Ida; Ferella, Francesco; Beolchini, Francesca; Kopacek, Bernd; Vegliò, Francesco

    2013-01-01

    Highlights: • Treatment of fluorescent powder of CRT waste. • Factorial experimental designs to study acid leaching of fluorescent powder and the purification of leach liquors. • Recover of yttrium by precipitation using oxalic acid. • Suitable flowsheet to recover yttrium from fluorescent powder. - Abstract: This work is focused on the recovery of yttrium and zinc from fluorescent powder of cathode ray tube (CRT). Metals are extracted by sulphuric acid in the presence of hydrogen peroxide. Leaching tests are carried out according to a 2 2 full factorial plan and the highest extraction yields for yttrium and zinc equal to 100% are observed under the following conditions: 3 M of sulphuric acid, 10% v/v of H 2 O 2 concentrated solution at 30% v/v, 10% w/w pulp density, 70 °C and 3 h of reaction. Two series of precipitation tests for zinc are carried out: a 2 2 full factorial design and a completely randomized factorial design. In these series the factors investigated are pH of solution during the precipitation and the amount of sodium sulphide added to precipitate zinc sulphide. The data of these tests are used to describe two empirical mathematical models for zinc and yttrium precipitation yields by regression analysis. The highest precipitation yields for zinc are obtained under the following conditions: pH equal to 2–2.5% and 10–12% v/v of Na 2 S concentrated solution at 10% w/v. In these conditions the coprecipitation of yttrium is of 15–20%. Finally further yttrium precipitation experiments by oxalic acid on the residual solutions, after removing of zinc, show that yttrium could be recovered and calcined to obtain the final product as yttrium oxide. The achieved results allow to propose a CRT recycling process based on leaching of fluorescent powder from cathode ray tube and recovery of yttrium oxide after removing of zinc by precipitation. The final recovery of yttrium is 75–80%

  10. Recovery of yttrium from fluorescent powder of cathode ray tube, CRT: Zn removal by sulphide precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Innocenzi, Valentina, E-mail: valentina.innocenzi1@univaq.it [Department of Industrial Engineering and Information and Economy, University of L’Aquila, Via Giovanni Gronchi n.18, Nucleo Ind.le di Pile, 67100 L’Aquila (Italy); De Michelis, Ida; Ferella, Francesco [Department of Industrial Engineering and Information and Economy, University of L’Aquila, Via Giovanni Gronchi n.18, Nucleo Ind.le di Pile, 67100 L’Aquila (Italy); Beolchini, Francesca [Department of Marine Sciences, Polytechnic Institute of Marche, Via Brecce Bianche, 60131 Ancona (Italy); Kopacek, Bernd [SAT, Austrian Society for Systems Engineering and Automation, Gurkasse 43/2, A-1140 Vienna (Austria); Vegliò, Francesco [Department of Industrial Engineering and Information and Economy, University of L’Aquila, Via Giovanni Gronchi n.18, Nucleo Ind.le di Pile, 67100 L’Aquila (Italy)

    2013-11-15

    Highlights: • Treatment of fluorescent powder of CRT waste. • Factorial experimental designs to study acid leaching of fluorescent powder and the purification of leach liquors. • Recover of yttrium by precipitation using oxalic acid. • Suitable flowsheet to recover yttrium from fluorescent powder. - Abstract: This work is focused on the recovery of yttrium and zinc from fluorescent powder of cathode ray tube (CRT). Metals are extracted by sulphuric acid in the presence of hydrogen peroxide. Leaching tests are carried out according to a 2{sup 2} full factorial plan and the highest extraction yields for yttrium and zinc equal to 100% are observed under the following conditions: 3 M of sulphuric acid, 10% v/v of H{sub 2}O{sub 2} concentrated solution at 30% v/v, 10% w/w pulp density, 70 °C and 3 h of reaction. Two series of precipitation tests for zinc are carried out: a 2{sup 2} full factorial design and a completely randomized factorial design. In these series the factors investigated are pH of solution during the precipitation and the amount of sodium sulphide added to precipitate zinc sulphide. The data of these tests are used to describe two empirical mathematical models for zinc and yttrium precipitation yields by regression analysis. The highest precipitation yields for zinc are obtained under the following conditions: pH equal to 2–2.5% and 10–12% v/v of Na{sub 2}S concentrated solution at 10% w/v. In these conditions the coprecipitation of yttrium is of 15–20%. Finally further yttrium precipitation experiments by oxalic acid on the residual solutions, after removing of zinc, show that yttrium could be recovered and calcined to obtain the final product as yttrium oxide. The achieved results allow to propose a CRT recycling process based on leaching of fluorescent powder from cathode ray tube and recovery of yttrium oxide after removing of zinc by precipitation. The final recovery of yttrium is 75–80%.

  11. In vitro cytotoxicity tests of ZnO‐Bi{sub 2}O{sub 3}‐Mn{sub 2}O{sub 3}-based varistor fabricated from ZnO micro and nanoparticle powders on L929 mouse cells

    Energy Technology Data Exchange (ETDEWEB)

    Sendi, Rabab Khalid, E-mail: last-name3@hotmail.com, E-mail: shahromx@hotmail.com, E-mail: ameerah7@hotmail.com; Mahmud, Shahrom, E-mail: last-name3@hotmail.com, E-mail: shahromx@hotmail.com, E-mail: ameerah7@hotmail.com; Munshi, Ayman, E-mail: last-name3@hotmail.com, E-mail: shahromx@hotmail.com, E-mail: ameerah7@hotmail.com [Nano-optoelectronics Research and Technology Laboratory (N.O.R.), School of Physics, Universiti Sains Malaysia, 11800, Penang (Malaysia); Seeni, Azman, E-mail: azanseeni@gmail.com [Advanced Medical and Dental Institute (AMDI), Universiti Sains Malaysia, 13200, Bertam, Pulau Pinang (Malaysia)

    2014-10-24

    The present study investigated the cytotoxicity of ZnO‐Bi{sub 2}O{sub 3}‐Mn{sub 2}O{sub 3}-varistors. To this effect, ZnO‐Bi{sub 2}O{sub 3}‐Mn{sub 2}O{sub 3} varistors fabricated from ZnO micro-and nanoparticle powders are prepared via conventional ceramic processing method. The effects of ZnO particle size on the properties of ZnO varistors are also investigated. The strong solid-state reaction during sintering may be attributed to the high surface area of the 20 nm ZnO nanoparticles that promote strong surface reaction. The intensity of XRD peaks reflected the high degree of crystallinity of the ZnO nanoparticles. However, the width of the peaks in case of ZnO nanoparticles has increased due to the quantum size effect. The cytotoxicity evaluation of ZnO varistor was conducted on mouse connective tissue fibroblast cells (L929) using Trypan Blue Exclusion Assay analysis. The results show that the four types of varistor samples lead to cellular mitochondrial dysfunction, morphological modifications and apoptosis at the various concentration range and the toxic effects are obviously displayed in high concentration samples. 20nm-VDR is the most toxic materials followed by 40nm-VDR, P8-VDR, and W4-VDR in a descending order.

  12. Kinetic Study of Zn2+ and Cd2+ Ions Sorption by Ceric Oxide Powder

    International Nuclear Information System (INIS)

    Hassan, H.S.; Abd El-Rahman, K.M.; El Sayed, A.A.

    2008-01-01

    Ceric Oxide powder was chemically synthesized and characterized using infrared spectra and x-ray diffraction. The sorptive removal of Zinc and Cadmium ions from aqueous waste solution using synthetic ceric oxide powder was investigated using batch technique. Experiments were carried out as a function of ph, particle size, solute concentration and temperature. The uptake of zinc was found to be greater than that of cadmium. A comparison of kinetic models applied to the sorption process of each ion was evaluated for the pseudo first order, the pseudo second order, and homogeneous particle diffusion kinetic models, respectively. The results showed that both the pseudo second order and the homogeneous particle diffusion model (HPDM) were found to best correlate the experimental rate data. The numerical values of the rate constants and particle diffusion coefficients were determined from the graphical representation of the proposed models. Activation energy (Ε a ) and entropy (δ S * ) of activation for each sorption process were also calculated from the linearized form of Arrhenius equation

  13. Fabrication, characterization and application of Cu{sub 2}ZnSn(S,Se){sub 4} absorber layer via a hybrid ink containing ball milled powders

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chunran [State Key Laboratory of Superhard Materials and College of Physics, Jilin University, Changchun 130023 (China); Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), College of Physics, Jilin University, Changchun 130012 (China); College of Mathematics and Physics, Bohai University, Jinzhou 121013 (China); Yao, Bin, E-mail: binyao@jlu.edu.cn [State Key Laboratory of Superhard Materials and College of Physics, Jilin University, Changchun 130023 (China); Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), College of Physics, Jilin University, Changchun 130012 (China); Li, Yongfeng, E-mail: liyongfeng@jlu.edu.cn [Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), College of Physics, Jilin University, Changchun 130012 (China); Xiao, Zhenyu [State Key Laboratory of Superhard Materials and College of Physics, Jilin University, Changchun 130023 (China); Ding, Zhanhui [Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), College of Physics, Jilin University, Changchun 130012 (China); Zhao, Haifeng; Zhang, Ligong; Zhang, Zhenzhong [State Key Laboratory of Luminescence and Applications, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, No. 3888 Dongnanhu Road, Changchun 130033 (China)

    2015-09-15

    Highlights: • CZTS powders are prepared from binary sulfides by a low cost ball milling process. • Elaborated on phase evolution and formation mechanism of CZTS. • Proposed a hybrid ink approach to resolve difficulty in deposition of CZTS film. • CZTSSe solar cells with highest efficiency of 4.2% are fabricated. • Small-grained CZTS layer hinders the collection of minority carriers. - Abstract: Cu{sub 2}ZnSnS{sub 4} (CZTS) powder with kesterite structure was prepared by ball milling of mixture of Cu{sub 2}S, ZnS and SnS{sub 2} powders for more than 15 h. By dispersing the milled CZTS powder in a Cu-, Zn- and Sn-chalcogenide precursor solution, a hybrid ink was fabricated. With the hybrid ink, a precursor CZTS film was deposited on Mo coated soda-lime glass by spin-coating. In order to obtain Cu{sub 2}ZnSn(S,Se){sub 4} (CZTSSe) absorber film with kesterite structure, the CZTS film was annealed at 560 °C for 15 min in Se ambient. It is demonstrated that the annealed film is dominated by a thick layer of kesterite CZTSSe with larger grain size and Cu{sub 8}Fe{sub 3}Sn{sub 2}(S,Se){sub 12} impurity phase with the exception of a very thin layer of kesterite CZTS with smaller grain size at interface between the CZTSSe and Mo layers. Solar cell device was fabricated by using the annealed CZTSSe film as absorber layer, and its conversion efficiency reached 4.2%. Mechanism of formation of the kesterite CZTS powder and CZTSSe film as well as effect of impurity phases on conversion efficiency are discussed in the present paper. The present results suggest that the hybrid ink approach combining with ball milling is a simple, low cost and promising method for preparation of kesterite CZTSSe absorber film and CZTSSe-based solar cell.

  14. On the sol-gel synthesis and thermal, structural, and magnetic studies of transition metal (Ni, Co, Mn) containing ZnO powders

    Energy Technology Data Exchange (ETDEWEB)

    Thota, Subhash; Dutta, Titas; Kumar, Jitendra [Materials Science Programme, Indian Institute of Technology Kanpur, Kanpur-208016 (India)

    2006-03-01

    Transition metal containing ZnO powders (Zn{sub 1-x}M{sub x}O, 0{<=}x{<=}0.30; M = Ni, Mn, Co) have been synthesized by a sol-gel process using zinc acetate dihydrate, respective acetate and oxalic acid as precursors with ethanol as a solvent. The process essentially involves gel formation, drying at 80 {sup 0}C for 24 h to provide the oxalate, and calcination at 500 {sup 0}C for 2 h to undergo an exothermic reaction and yield Zn{sub 1-x}M{sub x}O powder. Their XRD patterns correspond to a wurtzite hcp structure similar to that of pure ZnO, but with the lattice parameters varying slightly with type and extent of doping. It is shown that the dissolution of nickel and cobalt in ZnO is less than 10 at.%, whereas that of manganese lies between 10 and 15 at.%. Other phases that emerge include NiO (hexagonal, a = 2.954 A, c = 7.236 A), ZnCo{sub 2}O{sub 4} (cubic, a = 8.094 A) and ZnMnO{sub 3} (cubic, a = 8.35 A) in the Ni, Co and Mn containing ZnO systems, respectively. Observations of hysteresis loops both at 10 and 320 K and the nature of ESR spectra provide evidence for the ferromagnetic state in nickel containing ZnO powder. Besides, the deviation occurs in the magnetization versus temperature curves in zero field cooled (ZFC) and field cooled (FC) conditions (blocking temperature T{sub B} being 32 K for 5 at.% Ni). The magnetic behaviour of manganese and cobalt doped zinc oxide is, however, different, namely (i) no hysteresis loops (ii) decrease in magnetization with increase of Mn or Co content, and (iii) identical M-T curves under ZFC and FC conditions. The inverse susceptibility versus temperature curves of Zn{sub 1-x}Mn{sub x}O compounds reveal ferrimagnetism with Neel temperature T{sub N} of 4 K for x = 0.02, but antiferromagnetism for x = 0.15 and 0.25 with Curie-Weiss temperature of -43 and -30 K, respectively.

  15. Template-free synthesis of ZnWO{sub 4} powders via hydrothermal process in a wide pH range

    Energy Technology Data Exchange (ETDEWEB)

    Hojamberdiev, Mirabbos, E-mail: mirabbos_uz@yahoo.com [Shaanxi Key Laboratory of Nano-materials and Technology, Xi' an University of Architecture and Technology, Xi' an 710055 (China); Zhu, Gangqiang [School of Physics and Information Technology, Shaanxi Normal University, Xi' an 710062 (China); Xu, Yunhua [Shaanxi Key Laboratory of Nano-materials and Technology, Xi' an University of Architecture and Technology, Xi' an 710055 (China)

    2010-12-15

    ZnWO{sub 4} powders with different morphologies were fabricated through a template-free hydrothermal method at 180 {sup o}C for 8 h in a wide pH range. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-visible and luminescence spectrophotometers were applied to study the effects of pH values on crystallinity, morphology, optical and luminescence properties. The XRD results showed that the WO{sub 3} + ZnWO{sub 4}, ZnWO{sub 4}, and ZnO phases could form after hydrothermal processing at 180 {sup o}C for 8 h with the pH values of 1, 3-11, and 13, respectively. The SEM and TEM observation revealed that the morphological transformation of ZnWO{sub 4} powders occurred with an increase in pH values as follows: star anise-, peony-, and desert rose-like microstructures and soya bean- and rod-like nanostructures. The highest luminescence intensity was found to be in sample consisting of star anise-like crystallites among all the samples due to the presence of larger particles with high crystallinity resulted from the favorable pH under the current hydrothermal conditions.

  16. Processes of microstructural evolution during high-energy mechanical treatment of ZnO and black NiO powder mixture

    Energy Technology Data Exchange (ETDEWEB)

    Kakazey, M., E-mail: kakazey@hotmail.com [Centro de Investigación en Ingeniería y Ciencias Aplicadas, Universidad Autonoma del Estado de Morelos, Cuernavaca (Mexico); Vlasova, M. [Centro de Investigación en Ingeniería y Ciencias Aplicadas, Universidad Autonoma del Estado de Morelos, Cuernavaca (Mexico); Vorobiev, Y. [Unidad Querétaro del Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Querétaro (Mexico); Leon, I. [Centro de Investigaciones Quimicas, Universidad Autonoma del Estado de Morelos, Cuernavaca (Mexico); Cabecera Gonzalez, M. [Facultad de Ciencias Químicas e Ingeniería, Universidad Autonoma del Estado de Morelos, Cuernavaca (Mexico); Chávez Urbiola, Edgar Arturo [Unidad Querétaro del Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Querétaro (Mexico)

    2014-11-15

    Kinetics of microstructural evolution in ZnO and NiO black powder mixture during prolonged high-energy mechanical ball milling were investigated by Scanning Electron Microscopy, Laser Particle Sizer, X-ray diffraction, Electron Paramagnetic Resonance, Fourier Transform Infrared Spectroscopy and UV–vis Diffuse Reflection methods. The use of these methods allows us to control the macrostructural processes (ZnO particles and NiO granules grinding, the deagglomeration and “secondary agglomeration”), the microstructural processes (formation and annealing of different native defects in ZnO [V{sub Zn}{sup −}:Zn{sub i}{sup 0} (I), V{sub Zn}{sup −} (II), and (V{sub Zn}{sup −}){sub 2}{sup −} (III) centers] and NiO black) and the mechanothermal processes in samples. This allows to establish the relationship between microstructural evolution and the properties of the samples depending on the duration of the mechanical processing.

  17. Characterisation and Treatment of Nano-sized Particles, Colloids and Associated Polycyclic Aromatic Hydrocarbons in Stormwater

    DEFF Research Database (Denmark)

    Nielsen, Katrine

    such as pH, Total Suspended Solid(TSS), turbidity, and electrical conductivity.The five sites where stormwater was sampled from used two different methods of stormwater treatment: settling and filtration, and four different treatment techniques: detention ponds, stormwater pond, disc filter and combined...... sedimentation tanks. From all sites, inlet and outlet stormwater were collected,and pollutant concentrations were quantified as well as the removal efficiencies calculated. The colloidal and nano-sized particle-enhanced transportation of pollutants was also scrutinised in the stormwater.The μm-range PSD...

  18. Laser induced morphology change of silver colloids: formation of nano-size wires

    International Nuclear Information System (INIS)

    Tsuji, Takeshi; Watanabe, Norihisa; Tsuji, Masaharu

    2003-01-01

    We have performed laser irradiation at 355 nm onto spherical silver colloids in pure water, which were prepared by laser ablation of silver plate in pure water. In addition to size-reduced particles due to fragmentation, we have found that nano-size wire structures were formed in solution for the first time. The width of the wires was in the 10-100 nm range, and the length of long wires was more than 1 μm. Electron diffraction patterns revealed that these wires were composed of pure silver. It was suggested that the wires were formed via fusion of particles photo-thermally melted by laser irradiation

  19. Hydrodeoxygenation of fatty acid esters catalyzed by Ni on nano-sized MFI type zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Schreiber, Moritz W.; Rodriguez-Niño, Daniella; Gutiérrez, Oliver Y.; Lercher, Johannes A.

    2016-01-01

    The impact of support morphology and composition on the intrinsic activity of Ni supported on MFI-type zeolite was explored in the hydrodeoxygenation of methyl stearate, tristearate, and algae oil (mixture of triglycerides). The nano-sized structure of the support (self-pillared nanosheets) is beneficial for the activity of the catalysts. Higher Ni dispersion and concomitant higher reaction rates were obtained on nano-structured supports than on zeolite with conventional morphology. Rates normalized to accessible Ni atoms (TOF), however, varied little with support morphology. Acidity of the support increases the rate of Ni-catalyzed C-O hydrogenolysis per surface metal site.

  20. Synthesis of nanocrystalline NiO/ZnO heterostructured composite powders by sol-gel auto combustion method and their characterizations

    Science.gov (United States)

    Tangcharoen, Thanit; Klysubun, Wantana; Kongmark, Chanapa

    2018-03-01

    Nanocrystalline NiO/ZnO heterostructured composite powders were prepared by the sol-gel auto combustion method, based on nickel and zinc nitrate precursors and using diethanolamine (DEA) as novel fuel. The composition of different NiO and ZnO ratios, ranging from 100/0, 95/5, 90/10, 80/20, 60/40, 50/50, 40/60, 20/80, 10/90, 5/95 to 0/100, were studied. The structural, chemical bonding, morphological, optical, and fluorescence properties including the local atomic structure of each calcined sample were systematically investigated by means of X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), UV-visible diffuse reflectance spectroscopy (UV-DRS), photoluminescence (PL) spectroscopy, and synchrotron X-ray absorption spectroscopy (XAS), respectively. For the ZnO concentration below 20%, both XRD and Raman spectroscopy results revealed only the NiO phase. This conformed to the observation of Zn K-edge and Ni K-edge X-ray absorption near edge structure (XANES). The Zn ions found in the samples of low ZnO concentration exhibited six-fold coordination with oxygen atoms rather than the four-fold coordination found in the wurtzite (WZ) structure of ZnO. In contrast, the Ni ions which are found in the samples of low NiO concentration (≤10%) are coordinated both tetrahedrally and octahedrally by four or six oxygen atoms, respectively, rather than the six-fold coordination which is usually observed for Ni ions in the rock salt (RS) form of NiO. All analytical results obtained from experimental XANES spectra were verified by the theoretical calculation of absorption spectra using the FEFF9.7 code. The UV-DRS results showed that there was an increase in the reflectance efficiency for both infrared and visible light conditions as the content of ZnO increases; meanwhile, the values for the energy gap (Eg) of all composite samples were higher than that of pure NiO and ZnO. In addition, the PL spectra revealed major blue emission bands observed at 490

  1. Proficiency test Plant 6 - determination of As, Cd, Cu, Hg, Pb, Se and Zn in dry mushroom powder (Suillus bovinus)

    International Nuclear Information System (INIS)

    Polkowska-Motrenko, H.; Dudek, J.; Chajduk, E.; Sypula, M.; Sadowska-Bratek, M.

    2006-01-01

    Proficiency testing scheme PLANT 6: Determination of As, Cd, Cu, Hg, Pb, Se and Zn in dry mushroom powder (Suillus bovinus) has been described. The proficiency test has been provided by the Institute of Nuclear Chemistry and Technology (Warsaw) with cooperation with POLLAB-CHEM/EURACHEM-PL and REFMAT Society. Wild mushrooms were collected in the forest in north-west Poland, cleaned, i.e. dust, soil and attached mosses were removed. Mushrooms were cut into smaller parts and air dried in a dryer. Dried mushrooms were milled in a centrifugal mill and sieved. Particles of fraction below 1 mm diameter were collected. Analytical samples of 20 g mass were prepared. The material were then characterized by homogeneity testing and determination of assigned values for concentration of elements in question. The testing samples were sent to the laboratories participating in the proficiency test. The results supplied by the participants were statistically evaluated and the calculated values of z-score and En numbers were used for the evaluation of the participating laboratory competency. (author)

  2. Nano sized bismuth oxy chloride by metal organic chemical vapour deposition

    Energy Technology Data Exchange (ETDEWEB)

    Jagdale, Pravin, E-mail: pravin.jagdale@polito.it [Department of Applied Science and Technology (DISAT), Politecnico di Torino, 10129 (Italy); Castellino, Micaela [Center for Space Human Robotics, Istituto Italiano di Tecnologia, Corso Trento 21, 10129 Torino (Italy); Marrec, Françoise [Laboratory of Condensed Matter Physics, University of Picardie Jules Verne (UPJV), Amiens 80039 (France); Rodil, Sandra E. [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexicom (UNAM), Mexico D.F. 04510 (Mexico); Tagliaferro, Alberto [Department of Applied Science and Technology (DISAT), Politecnico di Torino, 10129 (Italy)

    2014-06-01

    Metal organic chemical vapour deposition (MOCVD) method was used to prepare thin films of bismuth based nano particles starting from bismuth salts. Nano sized bismuth oxy chloride (BiOCl) crystals were synthesized from solution containing bismuth chloride (BiCl{sub 3}) in acetone (CH{sub 3}-CO-CH{sub 3}). Self-assembly of nano sized BiOCl crystals were observed on the surface of silicon, fused silica, copper, carbon nanotubes and aluminium substrates. Various synthesis parameters and their significant impact onto the formation of self-assembled nano-crystalline BiOCl were investigated. BiOCl nano particles were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy and Micro-Raman spectroscopy. These analyses confirm that bismuth nanometer-sized crystal structures showing a single tetragonal phase were indeed bismuth oxy chloride (BiOCl) square platelets 18–250 nm thick and a few micrometres wide.

  3. Vaccine delivery system for tuberculosis based on nano-sized hepatitis B virus core protein particles

    Directory of Open Access Journals (Sweden)

    Dhanasooraj D

    2013-02-01

    Full Text Available Dhananjayan Dhanasooraj, R Ajay Kumar, Sathish MundayoorMycobacterium Research Group, Rajiv Gandhi Centre for Biotechnology, Kerala, IndiaAbstract: Nano-sized hepatitis B virus core virus-like particles (HBc-VLP are suitable for uptake by antigen-presenting cells. Mycobacterium tuberculosis antigen culture filtrate protein 10 (CFP-10 is an important vaccine candidate against tuberculosis. The purified antigen shows low immune response without adjuvant and tends to have low protective efficacy. The present study is based on the assumption that expression of these proteins on HBc nanoparticles would provide higher protection when compared to the native antigen alone. The cfp-10 gene was expressed as a fusion on the major immunodominant region of HBc-VLP, and the immune response in Balb/c mice was studied and compared to pure proteins, a mixture of antigens, and fusion protein-VLP, all without using any adjuvant. The humoral, cytokine, and splenocyte cell proliferation responses suggested that the HBc-VLP bearing CFP-10 generated an antigen-specific immune response in a Th1-dependent manner. By virtue of its self-adjuvant nature and ability to form nano-sized particles, HBc-VLPs are an excellent vaccine delivery system for use with subunit protein antigens identified in the course of recent vaccine research.Keywords: Mycobacterium tuberculosis, VLP, hepatitis B virus core particle, CFP-10, self-adjuvant, vaccine delivery

  4. Recovery of manganese and zinc from spent Zn-C cell powder: Experimental design of leaching by sulfuric acid solution containing glucose.

    Science.gov (United States)

    Biswas, Ranjit K; Karmakar, Aneek K; Kumar, Sree L

    2016-05-01

    The spent Zn-C cell powder, containing ZnMn2O4, ZnO, MnO(OH) and possibly Mn2O3 and Mn3O4, can be leached by a sulfuric acid solution mixed with some glucose. The leaching is found to be dependent on solid to liquid (S/L) ratio, amount of glucose, concentration of sulfuric acid solution, time and pulp agitation speed. For 5g powder (S), 1h leaching time and 300rpm pulp agitation speed, two-level four-factor (2(4)) experimental designs have been carried out to derive models for extraction of both Mn(II) and Zn(II). Amount of glucose (G, g), concentration of H2SO4 solution (C, mol/L), volume of H2SO4 solution as leachant (L, mL) and leaching temperature (T, °C) are considered as factors (variables). The model in both cases consists of mean, factor effects and interaction effects. The four-factor interaction effect is observed in neither of the cases. Some two-factor and three-factor effects are found to have produced positive or negative contributions to dissolution percentage in both cases. The models are examined for comparison with experimental results with good fits and also used for optimization of factors. At optimized condition (G=0.50g, C=2mol/L, L=250mL and T=100°C), an aliquot of 5g powder in 1h and at 300rpm produces a solution containing (7.08±0.10)g/L Mn(II) and (2.20±0.06)g/L Zn(II) corresponding to almost 100% extraction of both metal ions. Copyright © 2015 Elsevier Ltd. All rights reserved.

  5. Characterisation of Mn0.63Zn0.37Fe2O4 powders after intensive milling and subsequent thermal treatment

    Directory of Open Access Journals (Sweden)

    Labus Nebojša

    2017-01-01

    Full Text Available Commercial Mn-Zn powder (Mn0.63Zn0.37Fe2O4, 93 wt. % and Fe2O3 7 wt. % was milled 0.5, 1, 2 and 4 hours in a planetary ball mill. The goal was to observe intensive milling influences on oxidation and reduction processes that will happen during subsequent heating. Powders were characterized with XRD, SEM and particle seizer. Subsequent heating was monitored on TGA/DTA in an air atmosphere. After compaction of the milled powders, sintering was also performed in a dilatometric device. Sintered specimens were characterized micro structurally with SEM on a fresh breakage. Obtained differential TGA diagrams suggest intensive changes during prolonged milling of the oxidation kinetics on heating. Ferrite powders changed with milling as well as with second run heating were characterized to enable determination of the potentially best ratio of milling and heating to be applied to obtain the desired microstructure. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. OI172057 and Grant no. III45014

  6. Nanocrystalline spinel ferrite (MFe2O4, M = Ni, Co, Mn, Mg, Zn) powders prepared by a simple aloe vera plant-extracted solution hydrothermal route

    International Nuclear Information System (INIS)

    Phumying, Santi; Labuayai, Sarawuth; Swatsitang, Ekaphan; Amornkitbamrung, Vittaya; Maensiri, Santi

    2013-01-01

    Graphical abstract: This figure shows the specific magnetization curves of the as-prepared MFe 2 O 4 (M = Ni, Co, Mn, Mg, Zn) powders obtained from room temperature VSM measurement. These curves are typical for a soft magnetic material and indicate hysteresis ferromagnetism in the field ranges of ±500 Oe, ±1000 Oe, and ±2000 Oe for the CoFe 2 O 4 , MgFe 2 O 4 and MnFe 2 O 4 respectively, whereas the samples of NiFe 2 O 4 and ZnFe 2 O 4 show a superparamagnetic behavior. Highlights: ► Nanocrystalline MFe 2 O 4 powders were synthesized by a novel hydrothermal method. ► Metal acetylacetonates and aloe vera plant-extracted solution are used. ► This biosynthetic route is very simple and provides high-yield oxide nanomaterials. ► XRD and TEM results indicate that the prepared samples have only spinel structure. ► The maximum M s of 68.9 emu/g at 10 kOe were observed for the samples of MnFe 2 O 4 . - Abstract: Nanocrystalline spinel ferrite MFe 2 O 4 (M = Ni, Co, Mn, Mg, Zn) powders were synthesized by a novel hydrothermal method using Fe(acac) 3 , M(acac) 3 (M = Ni, Co, Mn, Mg, Zn) and aloe vera plant extracted solution. The X-ray diffraction and selected-area electron diffraction results indicate that the synthesized nanocrystalline have only spinel structure without the presence of other phase impurities. The crystal structure and morphology of the spinel ferrite powders, as revealed by TEM, show that the NiFe 2 O 4 and CoFe 2 O 4 samples contain nanoparticles, whereas the MnFe 2 O 4 and MgFe 2 O 4 samples consist of many nanoplatelets and nanoparticles. Interestingly, the ZnFe 2 O 4 sample contains plate-like structure of networked nanocrystalline particles. Room temperature magnetization results show a ferromagnetic behavior of the CoFe 2 O 4 , MnFe 2 O 4 and MgFe 2 O 4 samples, whereas the samples of NiFe 2 O 4 and ZnFe 2 O 4 exhibit a superparamagnetic behavior

  7. Synthesis, structural characterization and selectively catalytic properties of metal-organic frameworks with nano-sized channels: A modular design strategy

    International Nuclear Information System (INIS)

    Qiu Lingguang; Gu Lina; Hu Gang; Zhang Lide

    2009-01-01

    Modular design method for designing and synthesizing microporous metal-organic frameworks (MOFs) with selective catalytical activity was described. MOFs with both nano-sized channels and potential catalytic activities could be obtained through self-assembly of a framework unit and a catalyst unit. By selecting hexaaquo metal complexes and the ligand BTC (BTC=1,3,5-benzenetricarboxylate) as framework-building blocks and using the metal complex [M(phen) 2 (H 2 O) 2 ] 2+ (phen=1,10-phenanthroline) as a catalyst unit, a series of supramolecular MOFs 1-7 with three-dimensional nano-sized channels, i.e. [M 1 (H 2 O) 6 ].[M 2 (phen) 2 (H 2 O) 2 ] 2 .2(BTC).xH 2 O (M 1 , M 2 =Co(II), Ni(II), Cu(II), Zn(II), or Mn(II), phen=1,10-phenanthroline, BTC=1,3,5-benzenetricarboxylate, x=22-24), were synthesized through self-assembly, and their structures were characterized by IR, elemental analysis, and single-crystal X-ray diffraction. These supramolecular microporous MOFs showed significant size and shape selectivity in the catalyzed oxidation of phenols, which is due to catalytic reactions taking place in the channels of the framework. Design strategy, synthesis, and self-assembly mechanism for the construction of these porous MOFs were discussed. - Grapical abstract: A modular design strategy has been developed to synthesize microporous metal-organic frameworks with potential catalytic activity by self-assembly of the framework-building blocks and the catalyst unit

  8. Fabrication of nano-sized metal patterns on flexible polyethylene-terephthalate substrate using bi-layer nanoimprint lithography

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Seon Yong; Jung, Ho Yong [Department of Materials Science and Engineering, Korea University, Seoul, 136-701 (Korea, Republic of); Jeong, Jun-Ho [Nano-Mechanical Systems Research Center, Korea Institute of Machinery and Materials, Yuseong-gu Daejeon, 305-343 (Korea, Republic of); Lee, Heon, E-mail: heonlee@korea.ac.k [Department of Materials Science and Engineering, Korea University, Seoul, 136-701 (Korea, Republic of)

    2009-05-29

    Polymer films are widely used as a substrate for displays and for solar cells since they are cheap, transparent and flexible, and their material properties are easy to design. Polyethylene-terephthalate (PET) is especially useful for various applications requiring transparency, flexibility and good thermal and chemical resistance. In this study, nano-sized metal patterns were fabricated on flexible PET film by using nanoimprint lithography (NIL). Water-soluble poly-vinyl alcohol (PVA) resin was used as a planarization and sacrificial layer for the lift-off process, as it does not damage the PET films and can easily be etched off by using oxygen plasma. NIL was used to fabricate the nano-sized patterns on the non-planar or flexible substrate. Finally, a nano-sized metal pattern was successfully formed by depositing the metal layer over the imprinted resist patterns and applying the lift-off process, which is economic and environmentally friendly, to the PET films.

  9. Superior high creep resistance of in situ nano-sized TiCx/Al-Cu-Mg composite.

    Science.gov (United States)

    Wang, Lei; Qiu, Feng; Zhao, Qinglong; Zha, Min; Jiang, Qichuan

    2017-07-03

    The tensile creep behavior of Al-Cu-Mg alloy and its composite containing in situ nano-sized TiC x were explored at temperatures of 493 K, 533 K and 573 K with the applied stresses in the range of 40 to 100 MPa. The composite reinforced by nano-sized TiC x particles exhibited excellent creep resistance ability, which was about 4-15 times higher than those of the unreinforced matrix alloy. The stress exponent of 5 was noticed for both Al-Cu-Mg alloy and its composite, which suggested that their creep behavior was related to dislocation climb mechanism. During deformation at elevated temperatures, the enhanced creep resistance of the composite was mainly attributed to two aspects: (a) Orowan strengthening and grain boundary (GB) strengthening induced by nano-sized TiC x particles, (b) θ' and S' precipitates strengthening.

  10. Photogenerated cathode protection properties of nano-sized TiO2/WO3 coating

    International Nuclear Information System (INIS)

    Zhou Minjie; Zeng Zhenou; Zhong Li

    2009-01-01

    Nano-sized TiO 2 /WO 3 bilayer coatings were prepared on type 304 stainless steel substrate by sol-gel method. The performance of photo-electrochemical and photogenerated cathode protection of the coating was investigated by the electrochemical method. The results show that the bilayer coating with four TiO 2 layers and three WO 3 layers exhibits the highest photo-electrochemical efficiency and the best corrosion resistance property. Type 304 stainless steel with the coating can maintain cathode protection for 6 h in the dark after irradiation by UV illumination for 1 h. In addition, the mechanism of the photogenerated cathode protection for the bilayer coating was also explored.

  11. An engineered polypeptide around nano-sized manganese-calcium oxide: copying plants for water oxidation.

    Science.gov (United States)

    Najafpour, Mohammad Mahdi; Ghobadi, Mohadeseh Zarei; Sarvi, Bahram; Haghighi, Behzad

    2015-09-14

    Synthesis of new efficient catalysts inspired by Nature is a key goal in the production of clean fuel. Different compounds based on manganese oxide have been investigated in order to find their water-oxidation activity. Herein, we introduce a novel engineered polypeptide containing tyrosine around nano-sized manganese-calcium oxide, which was shown to be a highly active catalyst toward water oxidation at low overpotential (240 mV), with high turnover frequency of 1.5 × 10(-2) s(-1) at pH = 6.3 in the Mn(III)/Mn(IV) oxidation range. The compound is a novel structural and efficient functional model for the water-oxidizing complex in Photosystem II. A new proposed clever strategy used by Nature in water oxidation is also discussed. The new model of the water-oxidizing complex opens a new perspective for synthesis of efficient water-oxidation catalysts.

  12. Preclinical safety assessments of nano-sized constructs on cardiovascular system toxicity: A case for telemetry.

    Science.gov (United States)

    Cheah, Hoay Yan; Kiew, Lik Voon; Lee, Hong Boon; Japundžić-Žigon, Nina; Vicent, Marίa J; Hoe, See Ziau; Chung, Lip Yong

    2017-11-01

    While nano-sized construct (NSC) use in medicine has grown significantly in recent years, reported unwanted side effects have raised safety concerns. However, the toxicity of NSCs to the cardiovascular system (CVS) and the relative merits of the associated evaluation methods have not been thoroughly studied. This review discusses the toxicological profiles of selected NSCs and provides an overview of the assessment methods, including in silico, in vitro, ex vivo and in vivo models and how they are related to CVS toxicity. We conclude the review by outlining the merits of telemetry coupled with spectral analysis, baroreceptor reflex sensitivity analysis and echocardiography as an appropriate integrated strategy for the assessment of the acute and chronic impact of NSCs on the CVS. Copyright © 2017 John Wiley & Sons, Ltd. Copyright © 2017 John Wiley & Sons, Ltd.

  13. Effect of nano-sized, elemental selenium supplement on the proteome of chicken liver.

    Science.gov (United States)

    Gulyas, G; Csosz, E; Prokisch, J; Javor, A; Mezes, M; Erdelyi, M; Balogh, K; Janaky, T; Szabo, Z; Simon, A; Czegledi, L

    2017-06-01

    The nano-sized (100-500 nm) selenium has higher bioavailability and relatively lower toxicity compared to other selenium forms. The objective of the present study was to compare liver proteome profiles of broiler chicken fed with control diet without Se supplementation and diet supplemented with nano-Se with 4.25 mg/kg DM. Differential proteome analyses were performed by two-dimensional gel electrophoresis (2D-PAGE) followed by tryptic digestion and protein identification by liquid chromatography-mass spectrometry (LC-MS). Seven hundred and eight spots were detected, and 18 protein spots showed significant difference in their intensity (p selenium supplementation induced a dietary stress. Selenium supplementation may influence the metabolism of fatty acids and carbohydrates and antioxidant system, and increase the quantity of cytoskeletal actin and the expression of actin regulatory protein as well. Journal of Animal Physiology and Animal Nutrition © 2016 Blackwell Verlag GmbH.

  14. Surface energy effect on free vibration of nano-sized piezoelectric double-shell structures

    Science.gov (United States)

    Fang, Xue-Qian; Zhu, Chang-Song; Liu, Jin-Xi; Liu, Xiang-Lin

    2018-01-01

    Combining Goldenveizer-Novozhilov shell theory, thin plate theory and electro-elastic surface theory, the size-dependent vibration of nano-sized piezoelectric double-shell structures under simply supported boundary condition is presented, and the surface energy effect on the natural frequencies is discussed. The displacement components of the cylindrical nano-shells and annular nano-plates are expanded as the superposition of standard Fourier series based on Hamilton's principle. The total stresses with consideration of surface energy effect are derived, and the total energy function is obtained by using Rayleigh-Ritz energy method. The free vibration equation is solved, and the natural frequency is analyzed. In numerical examples, it is found that the surface elastic constant, piezoelectric constant and surface residual stress show different effects on the natural frequencies. The effect of surface piezoelectric constant is the maximum. The effect of dimensions of the double-shell under different surface material properties is also examined.

  15. Stimulated Brillouin scattering of laser in semiconductor plasma embedded with nano-sized grains

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Giriraj, E-mail: grsharma@gmail.com [SRJ Government Girls’ College, Neemuch (M P) (India); Dad, R. C. [Government P G College, Mandsaur (M P) (India); Ghosh, S. [School of Studies in Physics, Vikram University, Ujjain, (M P) (India)

    2015-07-31

    A high power laser propagating through semiconductor plasma undergoes Stimulated Brillouin scattering (SBS) from the electrostrictively generated acoustic perturbations. We have considered that nano-sized grains (NSGs) ions are embedded in semiconductor plasma by means of ion implantation. The NSGs are bombarded by the surrounding plasma particles and collect electrons. By considering a negative charge on the NSGs, we present an analytically study on the effects of NSGs on threshold field for the onset of SBS and Brillouin gain of generated Brillouin scattered mode. It is found that as the charge on the NSGs builds up, the Brillouin gain is significantly raised and the threshold pump field for the onset of SBS process is lowered.

  16. Photocatalytic Degradation of Malachite Green Using Nano-sized cerium-iron Oxide

    Directory of Open Access Journals (Sweden)

    K. L. Ameta

    2014-05-01

    Full Text Available Nano-sized cerium-iron oxide nanoparticles has been synthesized, characterized and explored as an efficient photocatalyst for the photocatalytic degradation of malachite green. The effects of different variables on degradation of dye were optimized such as the pH of the dye solution, dye concentration, amount of photocatalyst and light intensity. About 91% degradation of dye of 2×10-5 M concentration was observed after 2 hours at 8.5 pH and 600 Wm-2 light intensity. The reason for the high catalytic activity of the synthesized nanoparticles is ascribed to the high surface area which determines the active sites of the catalyst and accelerates the photocatalytic degradation.

  17. Tailoring properties of porous Poly (vinylidene fluoride) scaffold through nano-sized 58s bioactive glass.

    Science.gov (United States)

    Shuai, Cijun; Huang, Wei; Feng, Pei; Gao, Chengde; Shuai, Xiong; Xiao, Tao; Deng, Youwen; Peng, Shuping; Wu, Ping

    2016-01-01

    The biological properties of porous poly (vinylidene fluoride) (PVDF) scaffolds fabricated by selective laser sintering were tailored through nano-sized 58s bioactive glass. The results showed that 58s bioactive glass distributed evenly in the PVDF matrix. There were some exposed particles on the surface which provided attachment sites for biological response. It was confirmed that the scaffolds had highly bioactivity by the formation of bone-like apatite in simulated body fluid. And the bone-like apatite became dense with the increase in 58s bioactive glass and culture time. Moreover, the scaffolds were suitable for cell adhesion and proliferation compared with the PVDF scaffolds without 58s bioactive glass. The research showed that the PVDF/58s bioactive glass scaffolds had latent application in bone tissue engineering.

  18. Preparation of nano-sized α-Al2O3 from oil shale ash

    International Nuclear Information System (INIS)

    An, Baichao; Wang, Wenying; Ji, Guijuan; Gan, Shucai; Gao, Guimei; Xu, Jijing; Li, Guanghuan

    2010-01-01

    Oil shale ash (OSA), the residue of oil shale semi-coke roasting, was used as a raw material to synthesize nano-sized α-Al 2 O 3 . Ultrasonic oscillation pretreatment followed by azeotropic distillation was employed for reducing the particle size of α-Al 2 O 3 . The structural characterization at molecular and nanometer scales was performed using X-ray diffraction (XRD), transmission electron microscopy (TEM), respectively. The interaction between alumina and n-butanol was characterized by Fourier transform infrared spectroscopy (FT-IR). The results revealed that the crystalline phase of alumina nanoparticles was regular and the well dispersed alumina nanoparticles had a diameter of 50-80 nm. In addition, the significant factors including injection rate of carbon oxide (CO 2 ), ultrasonic oscillations, azeotropic distillation and surfactant were investigated with respect to their effects on the size of the alumina particles.

  19. Internal distribution of micro- / nano-sized inorganic particles and their cytocompatibility

    Energy Technology Data Exchange (ETDEWEB)

    Abe, Shigeaki; Iwadera, Nobuki; Esaki, Mitsue; Kida, Ikuhiro; Akasaka, Tsukasa; Uo, Motohiro; Yawaka, Yasutaka; Watari, Fumio [Graduate School of Dental Medicine, Hokkaido University, Sapporo 060-8586 (Japan); Mutoh, Mami [School of Dental Medicine, Hokkaido University, Sapporo 060-8586 (Japan); Morita, Manabu [Department of Oral Health, Okayama University Graduate School of Medicine, Dentisity and Pharmaceutical Science, Okayama 700-8525 (Japan); Haneda, Koichi [Department of Information Technology and Electronics, Senshu University of Ishinomaki, Ishinomaki 986-8580 (Japan); Yonezawa, Tetsu, E-mail: sabe@den.hokudai.ac.jp [Graduate School of Engineering, Hokkaido University, Sapporo 060-8628 (Japan)

    2011-10-29

    Nano-sized materials have received much attention lately, both in terms of their multiple applications and their biocompatibility. From both viewpoints, understanding the biodistribution of administered nano-materials is very important. In this study, we succeeded in visualizing the biodistribution of administered nano-materials using a scanning X-ray analytical microscope and magnetic resonance imaging method. Quantitative observation was carried out by inductively coupled plasma - atomic emission spectroscopy. We observed that the administered nano-particles accumulated in the liver, lung and spleen of mice. To estimate their cytocompatibility, the nano-particles were exposed to human liver cells. The results suggested that the micro-/ nano- particles have good cytocompatibility, except for copper oxide nano-particles.

  20. Reflection characterization of nano-sized dielectric structure in Morpho butterfly wings

    Science.gov (United States)

    Zhu, Dong

    2017-10-01

    Morpho butterflies living in Central and South America are well-known for their structural-colored blue wings. The blue coloring originates from the interaction of light with nano-sized dielectric structures that are equipped on the external surface of scales covering over their wings. The high-accuracy nonstandard finite-difference time domain (NS-FDTD) method is used to investigate the reflection characterization from the nanostructures. In the NS-FDTD calculation, a computational model is built to mimic the actual tree-like multilayered structures wherever possible using the hyperbolic tangent functions. It is generally known that both multilayer interference and diffraction grating phenomena can occur when light enters the nano-sized multilayered structure. To answer the question that which phenomenon is mainly responsible for the blue coloring, the NS-FDTD calculation is performed under various incidence angles at wavelengths from 360 to 500 nm. The calculated results at one incident wavelength under different incidence angles are visualized in a two-dimensional mapping image, where horizontal and vertical axes are incidence and reflection angles, respectively. The images demonstrate a remarkable transition from a ring-like pattern at shorter wavelengths to a retro-reflection pattern at longer wavelengths. To clarify the origin of the pattern transition, the model is separated into several simpler parts and compared their mapping images with the theoretical diffraction calculations. It can be concluded that the blue coloring at longer wavelengths is mainly caused by the cooperation of multilayer interference and retro-reflection while the effect of diffraction grating is predominant at shorter wavelengths.

  1. Influence of PANI Additions on Methanol Sensing Properties of ZnO Thin Films

    International Nuclear Information System (INIS)

    Mohammad Hafizuddin Jumali; Norhashimah Ramli; Izura Izzuddin; Muhammad Yahaya; Muhamad Mat Salleh

    2011-01-01

    The influence of PANI additions on methanol sensing properties of ZnO thin films at room temperature had been investigated. Commercial poly aniline powder (PANI) was mixed into 3 mL ZnO solution in five different weight percentages namely 1.25, 2.50, 3.75, 5.00 and 6.25 % to obtain ZnO/ PANI composite solutions. These solutions were spin coated onto glass substrate to form thin films. Microstructural studies by FESEM indicated that ZnO/ PANI films showed porous structures with nano size grains. The thickness of the film increased from 55 to 256 nm, proportionate to increment of PANI. The presence of 2 adsorption peaks at ∼310 nm and ∼610 nm in UV-Vis spectrum proved that addition of PANI has modified the adsorption peak of ZnO film. Methanol vapour detection showed that addition of PANI into ZnO dramatically improved the sensing properties of the sensor. The sensors also exhibited good repeatability and reversibility. Sensor with the amount of PANI of 3.75 wt % exhibited the highest sensitivity with response and recovery time was about 10 and 80 s, respectively. The possible sensing mechanism of the sensor was also discussed in this article. (author)

  2. 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

  3. Minimum ignition energy of nano and micro Ti powder in the presence of inert nano TiO₂ powder.

    Science.gov (United States)

    Chunmiao, Yuan; Amyotte, Paul R; Hossain, Md Nur; Li, Chang

    2014-06-15

    The inerting effect of nano-sized TiO2 powder on ignition sensitivity of nano and micro Ti powders was investigated with a Mike 3 apparatus. "A little is not good enough" is also suitable for micro Ti powders mixed with nano-sized solid inertants. MIE of the mixtures did not significantly increase until the TiO2 percentage exceeded 50%. Nano-sized TiO2 powders were ineffective as an inertant when mixed with nano Ti powders, especially at higher dust loadings. Even with 90% nano TiO2 powder, mixtures still showed high ignition sensitivity because the statistic energy was as low as 2.1 mJ. Layer fires induced by ignited but unburned metal particles may occur for micro Ti powders mixed with nano TiO2 powders following a low level dust explosion. Such layer fires could lead to a violent dust explosion after a second dispersion. Thus, additional attention is needed to prevent metallic layer fires even where electric spark potential is low. In the case of nano Ti powder, no layer fires were observed because of less flammable material involved in the mixtures investigated, and faster flame propagation in nanoparticle clouds. Copyright © 2014 Elsevier B.V. All rights reserved.

  4. Characterization of Nano Sized Microstructures in Fe and Ni Base ODS Alloys Using Small Angle Neutron Scattering

    International Nuclear Information System (INIS)

    Han, Young-Soo; Jang, Jin-Sung; Mao, Xiaodong

    2015-01-01

    Ferritic ODS(Oxide-dispersion-strengthened) alloy is known as a primary candidate material of the cladding tubes of a sodium fast reactor (SFR) in the Generation IV research program. In ODS alloy, the major contribution to the enhanced high-temperature mechanical property comes from the existence of nano-sized oxide precipitates, which act as obstacles to the movement of dislocations. In addition for the extremely high temperature application(>950 .deg. C) of future nuclear system, Ni base ODS alloys are considered as candidate materials. Therefore the characterization of nano-sized microstructures is important for determining the mechanical properties of the material. Small angle neutron scattering (SANS) technique non-destructively probes structures in materials at the nano-meter length of scale (1 - 1000 nm) and has been a very powerful tool in a variety of scientific/engineering research areas. In this study, nano-sized microstructures were quantitatively analyzed by small angle neutron scattering. Quantitative microstructural information on nanosized oxide in ODS alloys was obtained from SANS data. The effects of the thermo mechanical treatment on the size and volume fraction of nano-sized oxides were analyzed. For 12Cr ODS alloy, the experimental A-ratio is two-times larger than the theoretical A-ratio., and this result is considered to be due to the imperfections included in YTaO 4 . For Ni base ODS alloy, the volume fraction of the mid-sized particles (- 30 nm) increases rapidly as hot extrusion temperature decreases

  5. Hybrid composites of nano-sized zero valent iron and covalent organic polymers for groundwater contaminant degradation

    DEFF Research Database (Denmark)

    Mines, Paul D.; Byun, J.; Hwang, Yuhoon

    Zero valent iron is commonly used in a variety of treatment technologies (e.g. permeable reactive barriers), though recently a heavier focus has been placed on nano-sized zero valent iron (nZVI). Having superior reductive properties and large surface areas, nZVI is ideal for the degradation of ch...

  6. Presence of nano-sized silica during in vitro digestion of foods containing silica as a food additive

    NARCIS (Netherlands)

    Peters, R.; Kramer, E.; Oomen, A.G.; Herrera Rivera, Z.E.; Oegema, G.; Tromp, P.C.; Fokkink, R.; Rietveld, A.; Marvin, H.J.P.; Weigel, S.; Peijnenburg, A.A.C.M.; Bouwmeester, H.

    2012-01-01

    The presence, dissolution, agglomeration state, and release of materials in the nano-size range from food containing engineered nanoparticles during human digestion is a key question for the safety assessment of these materials. We used an in vitro model to mimic the human digestion. Food products

  7. A Novel Approach of Using Ground CNTs as the Carbon Source to Fabricate Uniformly Distributed Nano-Sized TiCx/2009Al Composites.

    Science.gov (United States)

    Wang, Lei; Qiu, Feng; Ouyang, Licheng; Wang, Huiyuan; Zha, Min; Shu, Shili; Zhao, Qinglong; Jiang, Qichuan

    2015-12-17

    Nano-sized TiC x /2009Al composites (with 5, 7, and 9 vol% TiC x ) were fabricated via the combustion synthesis of the 2009Al-Ti-CNTs system combined with vacuum hot pressing followed by hot extrusion. In the present study, CNTs were used as the carbon source to synthesize nano-sized TiC x particles. An attempt was made to correlate the effect of ground CNTs by milling and the distribution of synthesized nano-sized TiC x particles in 2009Al as well as the tensile properties of nano-sized TiC x /2009Al composites. Microstructure analysis showed that when ground CNTs were used, the synthesized nano-sized TiC x particles dispersed more uniformly in the 2009Al matrix. Moreover, when 2 h-milled CNTs were used, the 5, 7, and 9 vol% nano-sized TiC x /2009Al composites had the highest tensile properties, especially, the 9 vol% nano-sized TiC x /2009Al composites. The results offered a new approach to improve the distribution of in situ nano-sized TiC x particles and tensile properties of composites.

  8. Compound Method to Disperse CaCO3 Nanoparticles to Nano-Size in Water.

    Science.gov (United States)

    Gu, Sui; Cai, Jihua; Wang, Jijun; Yuan, Ye; Chang, Dewu; Chikhotkin, Viktor F

    2015-12-01

    The invalidation of CaCO3 nanoparticles (nCaCO3) is often caused by the fact of agglomeration and inhomogeneous dispersion which limits its application into water-based drilling muds for low permeability reservoirs such as coalbed methane reservoir and shale gas/oil reservoir. Effective methods to disperse nCaCO3 to nano-size (≤ 100 nm) in water have seldom been reported. Here we developed a compound method containing mechanical stirring, ultrasonic treatment, the use of surfactant and stabilizer to disperse nCaCO3 in water. It comprises the steps adding 2% nCaCO3, 1% sodium dodecyl sulfonate (SDS), 2% cetyltrimethyl ammonium bromide (CTAB), 2% OP-10, 3% to 4% biopolymer (XC) in water successively, stirring it at a shear rate of 6000 to 8000 r/min for 15 minutes and treating it with ultrasonic at a frequency of 28 KHz for 30 to 40 minutes. The dispersed nCaCO3 was characterized with scanning electron microscope (SEM), transmission electron microscope (TEM) and particle size distribution (PSD) tests. We found that nCaCO3 could be dispersed to below 100 nm in water and the medium value of nCaCO3 was below 50 nm. This method paved the way for the utilization of nCaCO3 in drilling fluid and completion fluid for low permeability reservoirs such as coal seams and shale gas/oil formations.

  9. Decontamination of radioactive cesium in soil using nano-size metallic calcium dispersing

    International Nuclear Information System (INIS)

    Mitoma, Yoshiharu; Fukuoka, Takezo; Matsue, Hideaki; Kobayashi, Hidemasa; Shiraishi, Hiroaki; Kajitani, Mikio

    2013-01-01

    In Japan, the major concern on radioactive cesium ( 134 Cs and 137 Cs) deposition and soil contamination due to the emission form the Fukushima Dai-ichi nuclear power plant showed up after a massive quake on March 11, 2011. Soil contamination with radioactive cesium has a long-term radiological impact due to its long half-life (30 years for 137 Cs) and its high biological hazard. Therefore, much attention has been paid to decontaminate Cs-contaminated soil with washing and/or extraction by adopting solvents. However, such wet methods have some disadvantages, i.e. forming of secondary effluents and additional cost for their treatment. We have recently shown that the nano-size metallic calcium/calcium oxide/iron dispersing mixture (Fe-nCa) is most effective for heavy metals immobilization and volume reduction method under dry condition. Thus, we applied this method to treat real radioactive cesium contaminated soils in dry condition. Simple stirring of the contaminated soil with Fe-nCa achieved about above 90% of radioactive Cs decontamination rate and the volume reduction level also reached around 50-60%. In this paper, we showed the effectiveness of a Fe-nCa method for the rapid remediation and volume reduction method of real radioactive cesium contaminated soils under dry conditions and our challenges for sophistication applying machine and reagents. (author)

  10. Study of carbon-doped micro and nano sized alumina for radiation dosimetry applications

    International Nuclear Information System (INIS)

    Fontainha, C. C. P.; Alves, N.; Ferraz, W. B.; Faria, L. O.

    2017-10-01

    New materials have been widely investigated for ionizing radiation dosimetry for medical procedures. Carbon-doped doped alumina (Al 2 O 3 :C) have been proposed as thermoluminescent and photo luminescent dosimeters. In the present study nano and micro-sized alumina doped with different percentages of carbon, sintered under different atmosphere conditions, at temperatures ranging from 1300 to 1750 degrees Celsius, were sintered and their dosimetric characteristics for gamma fields were investigated. Among the investigated sample preparation methods, the micro-sized alumina doped with 0.01% of carbon and sintered at 1700 degrees Celsius under reducing atmosphere has presented the best Tl output, comparable to the best Tl sensitivities ever reported to alumina and better efficiency than the nano-sized alumina synthesized in this study. The influence of humidity in the Tl signal has been evaluated to be -4.0%. The micro-sized alumina obtained by the methodology used in this work is a suitable candidate for application in X and gamma radiation dosimetry. (Author)

  11. Amplified CPEs enhancement of chorioamnion membrane mass transport by encapsulation in nano-sized PLGA particles.

    Science.gov (United States)

    Azagury, Aharon; Amar-Lewis, Eliz; Appel, Reut; Hallak, Mordechai; Kost, Joseph

    2017-08-01

    Chemical penetration enhancers (CPEs) have long been used for mass transport enhancement across membranes. Many CPEs are used in a solution or gel and could be a solvent. The use of CPEs is mainly limited due to their toxicity/irritation levels. This study presents the evaluation of encapsulated CPEs in nano-sized polymeric particles on the chorioamnion (CA) membrane mass transport. CPEs' mass encapsulated in nanoparticles was decreased by 10,000-fold. Interestingly, this approach resulted in a 6-fold increase in mass transport across the CA. This approach may also be used with other CPEs' base applications necessitating lower CPE concentration. Applying Ultrasound (US) has shown to increase the release rate of and also the mass transport across the CA membrane. It is proposed that encapsulated CPEs penetrate into the CA membrane thus prolonging their exposure, possibly extending their penetration into the CA membrane, while insonation also deepens their penetration into the CA membrane. Copyright © 2017 Elsevier B.V. All rights reserved.

  12. Nano-sized copper tungstate thin films as positive electrodes for rechargeable Li batteries

    International Nuclear Information System (INIS)

    Li Chilin; Fu Zhengwen

    2008-01-01

    Nano-sized CuWO 4 thin films have been fabricated by radio-frequency (R.F.) sputtering deposition, and are used as positive electrode with both LiClO 4 liquid electrolyte and LiPON solid electrolyte in rechargeable lithium batteries. An initial discharge capacity of 192 and 210 mAh/g is obtainable for CuWO 4 film electrode with and without coated LiPON in liquid electrolyte, respectively. An all-solid-state cell with Li/LiPON/CuWO 4 layers shows a high-volume rate capacity of 145 μAh/cm 2 μm in first discharge, and overcomes the unfavorable electrochemical degradation observed in liquid electrolyte system. A two-step reactive mechanism is investigated by both transmission electron microscopy and selected area electron diffraction techniques. Apart from the extrusion and injection of Cu 2+ /Cu 0 , additional capacity can be achieved by the reversible reactivity of (WO 4 ) 2- framework. The chemical diffusion coefficients of Li intercalation/deintercalation are estimated by cyclic voltammetry. Nano-CuWO 4 thin film is expected to be a promising positive electrode material for high-performance rechargeable thin-film lithium batteries

  13. Spin-resolved magnetic studies of focused ion beam etched nano-sized magnetic structures

    International Nuclear Information System (INIS)

    Li Jian; Rau, Carl

    2005-01-01

    Scanning ion microscopy with polarization analysis (SIMPA) is used to study the spin-resolved surface magnetic structure of nano-sized magnetic systems. SIMPA is utilized for in situ topographic and spin-resolved magnetic domain imaging as well as for focused ion beam (FIB) etching of desired structures in magnetic or non-magnetic systems. Ultra-thin Co films are deposited on surfaces of Si(1 0 0) substrates, and ultra-thin, tri-layered, bct Fe(1 0 0)/Mn/bct Fe(1 0 0) wedged magnetic structures are deposited on fcc Pd(1 0 0) substrates. SIMPA experiments clearly show that ion-induced electrons emitted from magnetic surfaces exhibit non-zero electron spin polarization (ESP), whereas electrons emitted from non-magnetic surfaces such as Si and Pd exhibit zero ESP, which can be used to calibrate sputtering rates in situ. We report on new, spin-resolved magnetic microstructures, such as magnetic 'C' states and magnetic vortices, found at surfaces of FIB patterned magnetic elements. It is found that FIB milling has a negligible effect on surface magnetic domain and domain wall structures. It is demonstrated that SIMPA can evolve into an important and efficient tool to study magnetic domain, domain wall and other structures as well as to perform magnetic depth profiling of magnetic nano-systems to be used in ultra-high density magnetic recording and in magnetic sensors

  14. Prevention of dental erosion of a sports drink by nano-sized hydroxyapatite in situ study.

    Science.gov (United States)

    Min, Ji Hyun; Kwon, Ho Keun; Kim, Baek Il

    2015-01-01

    To evaluate the inhibitory effects of the sports drink containing nano-sized hydroxyapatite (nano-HA) on dental erosion in situ. The study had a single-blind, two-treatment crossover design. The two treatment groups were a control group (CG; Powerade only) and an experimental group (EG; 0.25% wt/vol nano-HA was added to Powerade). Ten subjects wore removable palatal appliances containing bovine enamel specimens. The appliances were immersed in each drink for 10 mins, 4 times a day for 10 days. The tooth surface microhardness (SMH) was tested, and the erosion depth and the morphology of the tooth surface were observed. The data were analysed by repeated measures anova and t-test. Between the baseline and the 10th day, SMH was decreased by 80% in the specimens of the CG (P erosion depth of 12.70 ± 4.66 μm and an irregular tooth surface were observed on the 10th day in the specimens of the CG. No dental erosions, however, was observed in the specimens of the EG. The sports drink containing 0.25% nano-HA was effective in preventing dental erosion in situ. © 2014 BSPD, IAPD and John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

  15. Preparation of Natural Rubber (NR) Based Nano-Sized Materials Using Sol-Gel Technique

    International Nuclear Information System (INIS)

    Dahlan Mohd; Mahathir Mohamed

    2011-01-01

    The objectives of this project are to prepare nano-sized natural rubber-based hybrid coating material by sol-gel technique; to explore the possibility of producing ENR-Si (epoxidized natural rubber-silica) cramer with toughening effects; and to use it in radiation curing of surface coating. Since early 1960s Malaysia has introduced various forms of value-added natural rubber such as Standard Malaysian Rubber (SMR), methylmethacrylate-grafted natural rubber (MG rubber), followed by liquid natural rubber and epoxidized natural rubber (ENR). Products such as liquid epoxidized natural rubber acrylate (LENRA) and thermoplastic natural rubber (TPNR) are still on-going research projects in Nuclear Malaysia. The former has strong possibility to be used as radiation-sensitive comparabilities in TPNR blends, besides its original purpose for example in radiation curing of surface coating. But earlier findings indicated that, to make it (as for surface coating) more effective, reinforcement system is needed to be introduced. Strong candidate is silica by sol-gel technique, since common reinforcement filler for example carbon black has drawbacks in this particular case. This technique was introduced in late 1960s to produce metal oxides such as silica and titanium oxides in solution. (author)

  16. Synthesis of bis- and tris(indolylmethanes catalyzed by an inorganic nano-sized catalyst followed by dehydrogenation to hyperconjugated products

    Directory of Open Access Journals (Sweden)

    Khorshidi Alireza

    2016-01-01

    Full Text Available A set of bis- and tris(indolylmethanes were prepared and dehydrogenated to their hyperconjugated products in a one-pot fashion. Nano-sized-SO3H functionalized mesoporous KIT-6 coated on magnetite nanoparticles (Fe3O4@SiO2@KIT-6-OSO3H was used as an efficient catalyst in the first step of synthesis, and dehydrogenation was performed by using (NH42S2O8 after removal of the catalyst. The catalyst was fully characterized by Fourier transform infrared spectroscopy (FT-IR, transmission electron microscopy (TEM and X-ray powder diffraction (XRD, as well as nitrogen adsorption-desorption isotherms. The bis- and tris(indolylmethanes were studied by UV-Vis spectroscopy before and after dehydrogenation, and effect of the ambient parameters on their spectra was investigated. It was found that bis- and tris(indolylmethanes have no considerable absorption in the visible range and what makes them colorful is partial dehydrogenation due to exposure to air. Our catalyst as a new combination of known materials, showed superiority in terms of yield, time, and mild reaction conditions in comparison with previous reports.

  17. Fabrication and anti-frosting performance of super hydrophobic coating based on modified nano-sized calcium carbonate and ordinary polyacrylate

    Energy Technology Data Exchange (ETDEWEB)

    Wang Hao [Department of Chemical Engineering, Tsinghua University, Beijing 100084 (China); Tang Liming [Department of Chemical Engineering, Tsinghua University, Beijing 100084 (China)], E-mail: tanglm@mail.tsinghua.edu.cn; Wu Xiaomin; Dai Wantian [Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Qiu Yipeng [Department of Chemical Engineering, Tsinghua University, Beijing 100084 (China)

    2007-09-15

    Nano-sized calcium carbonate (CaCO{sub 3}) particles were modified by heptadecafluorodecyl trimethoxysilane under acidic water condition. An ordinary polyacrylate prepared via radical copolymerization of methyl methacrylate, butyl acrylate, acrylic acid and {beta}-hydroxyethyl methacrylate was used as the binder to form hydrophobic coatings with the modified CaCO{sub 3}. Super hydrophobic coating with water contact angle of 155{sup o} was obtained from modified CaCO{sub 3} and the polyacrylate at their weight ratio of 8/2 by a simple procedure. Based on surface analysis by scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS), the super hydrophobicity can be attributed to both the surface microstructure and surface enrichment of fluoroalkyl chains. Due to a low water sliding angle, carbon black powder on super hydrophobic surface was easily removed by rolling water droplet. Furthermore, the anti-frosting performance of different surfaces was investigated, which indicated that the frost formed on superhydrophobic surface was greatly retarded compared with that on bare copper surface. The surface kept super hydrophobicity even after freezing-thawing treatment for 10 times.

  18. Low Thermal Conductivity of Bulk Amorphous Si1- x Ge x Containing Nano-Sized Crystalline Particles Synthesized by Ball-Milling Process

    Science.gov (United States)

    Muthusamy, Omprakash; Nishino, Shunsuke; Ghodke, Swapnil; Inukai, Manabu; Sobota, Robert; Adachi, Masahiro; Kiyama, Makato; Yamamoto, Yoshiyuki; Takeuchi, Tsunehiro; Santhanakrishnan, Harish; Ikeda, Hiroya; Hayakawa, Yasuhiro

    2018-06-01

    Amorphous Si0.65Ge0.35 powder containing a small amount of nano-sized crystalline particles was synthesized by means of the mechanical alloying process. Hot pressing for 24 h under the pressure of 400 MPa at 823 K, which is below the crystallization temperature, allowed us to obtain bulk amorphous Si-Ge alloy containing a small amount of nanocrystals. The thermal conductivity of the prepared bulk amorphous Si-Ge alloy was extremely low, showing a magnitude of less than 1.35 Wm-1 K-1 over the entire temperature range from 300 K to 700 K. The sound velocity of longitudinal and transverse waves for the bulk amorphous Si0.65Ge0.35 were measured, and the resulting values were 5841 m/s and 2840 m/s, respectively. The estimated mean free path of phonons was kept at the very small value of ˜ 4.2 nm, which was mainly due to the strong scattering limit of phonons in association with the amorphous structure.

  19. Superior model for fault tolerance computation in designing nano-sized circuit systems

    Energy Technology Data Exchange (ETDEWEB)

    Singh, N. S. S., E-mail: narinderjit@petronas.com.my; Muthuvalu, M. S., E-mail: msmuthuvalu@gmail.com [Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, Perak (Malaysia); Asirvadam, V. S., E-mail: vijanth-sagayan@petronas.com.my [Electrical and Electronics Engineering Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, Perak (Malaysia)

    2014-10-24

    As CMOS technology scales nano-metrically, reliability turns out to be a decisive subject in the design methodology of nano-sized circuit systems. As a result, several computational approaches have been developed to compute and evaluate reliability of desired nano-electronic circuits. The process of computing reliability becomes very troublesome and time consuming as the computational complexity build ups with the desired circuit size. Therefore, being able to measure reliability instantly and superiorly is fast becoming necessary in designing modern logic integrated circuits. For this purpose, the paper firstly looks into the development of an automated reliability evaluation tool based on the generalization of Probabilistic Gate Model (PGM) and Boolean Difference-based Error Calculator (BDEC) models. The Matlab-based tool allows users to significantly speed-up the task of reliability analysis for very large number of nano-electronic circuits. Secondly, by using the developed automated tool, the paper explores into a comparative study involving reliability computation and evaluation by PGM and, BDEC models for different implementations of same functionality circuits. Based on the reliability analysis, BDEC gives exact and transparent reliability measures, but as the complexity of the same functionality circuits with respect to gate error increases, reliability measure by BDEC tends to be lower than the reliability measure by PGM. The lesser reliability measure by BDEC is well explained in this paper using distribution of different signal input patterns overtime for same functionality circuits. Simulation results conclude that the reliability measure by BDEC depends not only on faulty gates but it also depends on circuit topology, probability of input signals being one or zero and also probability of error on signal lines.

  20. Superior model for fault tolerance computation in designing nano-sized circuit systems

    International Nuclear Information System (INIS)

    Singh, N. S. S.; Muthuvalu, M. S.; Asirvadam, V. S.

    2014-01-01

    As CMOS technology scales nano-metrically, reliability turns out to be a decisive subject in the design methodology of nano-sized circuit systems. As a result, several computational approaches have been developed to compute and evaluate reliability of desired nano-electronic circuits. The process of computing reliability becomes very troublesome and time consuming as the computational complexity build ups with the desired circuit size. Therefore, being able to measure reliability instantly and superiorly is fast becoming necessary in designing modern logic integrated circuits. For this purpose, the paper firstly looks into the development of an automated reliability evaluation tool based on the generalization of Probabilistic Gate Model (PGM) and Boolean Difference-based Error Calculator (BDEC) models. The Matlab-based tool allows users to significantly speed-up the task of reliability analysis for very large number of nano-electronic circuits. Secondly, by using the developed automated tool, the paper explores into a comparative study involving reliability computation and evaluation by PGM and, BDEC models for different implementations of same functionality circuits. Based on the reliability analysis, BDEC gives exact and transparent reliability measures, but as the complexity of the same functionality circuits with respect to gate error increases, reliability measure by BDEC tends to be lower than the reliability measure by PGM. The lesser reliability measure by BDEC is well explained in this paper using distribution of different signal input patterns overtime for same functionality circuits. Simulation results conclude that the reliability measure by BDEC depends not only on faulty gates but it also depends on circuit topology, probability of input signals being one or zero and also probability of error on signal lines

  1. Nano-sized titanium dioxide toxicity in rat prostate and testis: Possible ameliorative effect of morin.

    Science.gov (United States)

    Shahin, Nancy N; Mohamed, Maha M

    2017-11-01

    This study investigated the effect of short-term oral exposure to nano-sized titanium dioxide (nTiO 2 ) on Wistar rat prostate and testis, and the associating reproductive-related alterations. The study also evaluated the potential ameliorative effect of the natural flavonoid, morin, on nTiO 2 -induced aberrations. Intragastric administration of nTiO 2 (50mg/kg/day for 1, 2 and 3weeks) increased testicular gamma-glutamyltransferase (γ-GT) activity and decreased testicular steroidogenic acute regulatory protein (StAR) and c-kit gene expression, serum testosterone level and sperm count. nTiO 2 -treated rats also exhibited prostatic and testicular altered glutathione levels, elevated TNF-α levels, up-regulated Fas, Bax and caspase-3 gene expression, down-regulated Bcl-2 gene expression and enhanced prostatic lipid peroxidation. Sperm malformation and elevated testicular acid phosphatase (ACP) activity and malondialdehyde level, serum prostatic acid phosphatase activity, prostate specific antigen (PSA), gonadotrophin and estradiol levels occurred after the 2 and 3week regimens. Morin (30mg/kg/day administered intragastrically for 5weeks) mitigated nTiO 2 -induced prostatic and testicular injury as evidenced by lowering serum PSA level, testicular γ-GT and ACP activities and TNF-α level, along with hampering both intrinsic and extrinsic apoptotic pathways. Moreover, morin alleviated prostatic lipid peroxidation, raised prostatic glutathione level, and relieved testicular reductive stress. Additionally, morin increased testicular StAR and c-kit mRNA expression, raised the sperm count, reduced sperm deformities and modified the altered hormone profile. Histopathological evaluation supported the biochemical findings. In conclusion, morin could ameliorate nTiO 2 -induced prostatic and testicular injury and the corresponding reproductive-related aberrations via redox regulatory, anti-inflammatory and anti-apoptotic mechanisms, promoting steroidogenesis and

  2. Nano sized Particles of Silica and Its Derivatives for Applications in Various Branches of Food and Nutrition Sectors

    International Nuclear Information System (INIS)

    Kasaai, M. R.

    2015-01-01

    Nano sized particles of silica and its derivatives have been identified as versatile for a broad range of science, technology, and engineering applications. In this paper, an effort has been made to provide a short review from the available literature information on their applications in various branches of food and nutrition sectors. The information provided in this paper describes various parameters affecting their performances and efficiencies. The properties and applications of nano silica and its derivatives have been compared with micro silica and bulk-silica for their performances. The use of nano sized particles of silica and its derivatives provides a number of advantages. Their efficiencies and performances are significantly higher than those of the traditional ones

  3. Structural elucidation and magnetic behavior evaluation of rare earth (La, Nd, Gd, Tb, Dy) doped BaCoNi-X hexagonal nano-sized ferrites

    Energy Technology Data Exchange (ETDEWEB)

    Majeed, Abdul, E-mail: abdulmajeed2276@gmail.com [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Khan, Muhammad Azhar, E-mail: azhar.khan@iub.edu.pk [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Raheem, Faseeh ur; Hussain, Altaf; Iqbal, F. [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Murtaza, Ghulam [Centre for Advanced Studies in Physics, Government College University, Lahore 54000 (Pakistan); Akhtar, Majid Niaz [Department of Physics, COMSATS Institute of Information Technology, Lahore 54000 (Pakistan); Shakir, Imran [Deanship of Scientific Research, College of Engineering, King Saud University, PO Box 800, Riyadh 11421 (Saudi Arabia); Warsi, Muhammad Farooq [Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan)

    2016-06-15

    Rare-earth (RE=La{sup 3+}, Nd{sup 3+}, Gd{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) doped Ba{sub 2}NiCoRE{sub x}Fe{sub 28−x}O{sub 46} (x=0.25) hexagonal ferrites were synthesized for the first time via micro-emulsion route, which is a fast chemistry route for obtaining nano-sized ferrite powders. These nanomaterials were investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), as well as vibrating sample magnetometer (VSM). The XRD analysis exhibited that all the samples crystallized into single X-type hexagonal phase. The crystalline size calculated by Scherrer's formula was found in the range 7–19 nm. The variations in lattice parameters elucidated the incorporation of rare-earth cations in these nanomaterials. FTIR absorption spectra of these X-type ferrites were investigated in the wave number range 500–2400 cm{sup −1.} Each spectrum exhibited absorption bands in the low wave number range, thereby confirming the X-type hexagonal structure. The enhancement in the coercivity was observed with the doping of rare-earth cations. The saturation magnetization was lowered owing to the redistribution of rare-earth cations on the octahedral site (3b{sub VI}). The higher values of coercivity (664–926 Oe) of these nanomaterials suggest their use in longitudinal recording media. - Graphical abstract: Nano-sized rare-earth (RE=La{sup 3+}, Nd{sup 3+}, Gd{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) doped Ba{sub 2}NiCoRE{sub x}Fe{sub 28−x}O{sub 46} (x=0.25) hexagonal ferrites were synthesized for the first time via micro-emulsion route and the crystallite size was found in the range 7–19 nm. The enhancement in the coercivity was observed with the doping of rare-earth cations. The higher values of coercivity (664–926 Oe) of these nanomaterials suggest their use in longitudinal recording media. - Highlights: • Micro-emulsion route was used to synthesize Ba{sub 2}NiCoRE{sub x}Fe{sub 28−x}O{sub 46} ferrites. • The crystallite size was found

  4. Structural elucidation and magnetic behavior evaluation of rare earth (La, Nd, Gd, Tb, Dy) doped BaCoNi-X hexagonal nano-sized ferrites

    International Nuclear Information System (INIS)

    Majeed, Abdul; Khan, Muhammad Azhar; Raheem, Faseeh ur; Hussain, Altaf; Iqbal, F.; Murtaza, Ghulam; Akhtar, Majid Niaz; Shakir, Imran; Warsi, Muhammad Farooq

    2016-01-01

    Rare-earth (RE=La 3+ , Nd 3+ , Gd 3+ , Tb 3+ , Dy 3+ ) doped Ba 2 NiCoRE x Fe 28−x O 46 (x=0.25) hexagonal ferrites were synthesized for the first time via micro-emulsion route, which is a fast chemistry route for obtaining nano-sized ferrite powders. These nanomaterials were investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), as well as vibrating sample magnetometer (VSM). The XRD analysis exhibited that all the samples crystallized into single X-type hexagonal phase. The crystalline size calculated by Scherrer's formula was found in the range 7–19 nm. The variations in lattice parameters elucidated the incorporation of rare-earth cations in these nanomaterials. FTIR absorption spectra of these X-type ferrites were investigated in the wave number range 500–2400 cm −1. Each spectrum exhibited absorption bands in the low wave number range, thereby confirming the X-type hexagonal structure. The enhancement in the coercivity was observed with the doping of rare-earth cations. The saturation magnetization was lowered owing to the redistribution of rare-earth cations on the octahedral site (3b VI ). The higher values of coercivity (664–926 Oe) of these nanomaterials suggest their use in longitudinal recording media. - Graphical abstract: Nano-sized rare-earth (RE=La 3+ , Nd 3+ , Gd 3+ , Tb 3+ , Dy 3+ ) doped Ba 2 NiCoRE x Fe 28−x O 46 (x=0.25) hexagonal ferrites were synthesized for the first time via micro-emulsion route and the crystallite size was found in the range 7–19 nm. The enhancement in the coercivity was observed with the doping of rare-earth cations. The higher values of coercivity (664–926 Oe) of these nanomaterials suggest their use in longitudinal recording media. - Highlights: • Micro-emulsion route was used to synthesize Ba 2 NiCoRE x Fe 28−x O 46 ferrites. • The crystallite size was found in the range 7–19 nm. • The rare-earth incorporation enhanced the coercivity (664–926 Oe).

  5. Origin of Capacity Fading in Nano-Sized Co3O4Electrodes: Electrochemical Impedance Spectroscopy Study

    Directory of Open Access Journals (Sweden)

    Kang Jin-Gu

    2008-01-01

    Full Text Available Abstract Transition metal oxides have been suggested as innovative, high-energy electrode materials for lithium-ion batteries because their electrochemical conversion reactions can transfer two to six electrons. However, nano-sized transition metal oxides, especially Co3O4, exhibit drastic capacity decay during discharge/charge cycling, which hinders their practical use in lithium-ion batteries. Herein, we prepared nano-sized Co3O4with high crystallinity using a simple citrate-gel method and used electrochemical impedance spectroscopy method to examine the origin for the drastic capacity fading observed in the nano-sized Co3O4anode system. During cycling, AC impedance responses were collected at the first discharged state and at every subsequent tenth discharged state until the 100th cycle. By examining the separable relaxation time of each electrochemical reaction and the goodness-of-fit results, a direct relation between the charge transfer process and cycling performance was clearly observed.

  6. Nano-sized metabolic precursors for heterogeneous tumor-targeting strategy using bioorthogonal click chemistry in vivo.

    Science.gov (United States)

    Lee, Sangmin; Jung, Seulhee; Koo, Heebeom; Na, Jin Hee; Yoon, Hong Yeol; Shim, Man Kyu; Park, Jooho; Kim, Jong-Ho; Lee, Seulki; Pomper, Martin G; Kwon, Ick Chan; Ahn, Cheol-Hee; Kim, Kwangmeyung

    2017-12-01

    Herein, we developed nano-sized metabolic precursors (Nano-MPs) for new tumor-targeting strategy to overcome the intrinsic limitations of biological ligands such as the limited number of biological receptors and the heterogeneity in tumor tissues. We conjugated the azide group-containing metabolic precursors, triacetylated N-azidoacetyl-d-mannosamine to generation 4 poly(amidoamine) dendrimer backbone. The nano-sized dendrimer of Nano-MPs could generate azide groups on the surface of tumor cells homogeneously regardless of cell types via metabolic glycoengineering. Importantly, these exogenously generated 'artificial chemical receptors' containing azide groups could be used for bioorthogonal click chemistry, regardless of phenotypes of different tumor cells. Furthermore, in tumor-bearing mice models, Nano-MPs could be mainly localized at the target tumor tissues by the enhanced permeation and retention (EPR) effect, and they successfully generated azide groups on tumor cells in vivo after an intravenous injection. Finally, we showed that these azide groups on tumor tissues could be used as 'artificial chemical receptors' that were conjugated to bioorthogonal chemical group-containing liposomes via in vivo click chemistry in heterogeneous tumor-bearing mice. Therefore, overall results demonstrated that our nano-sized metabolic precursors could be extensively applied to new alternative tumor-targeting technique for molecular imaging and drug delivery system, regardless of the phenotype of heterogeneous tumor cells. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. An understanding of anomalous capacity of nano-sized CoO anode materials for advanced Li-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Chen, C.H.; Venkateswarlu, M.; Cheng, M.Y.; Ragavendran, K.; Hwang, B.J. [Nano-Electrochemistry Lab., Department of Chemical Engineering, National Taiwan University of Science and Technology, 43 Keelung Rd., Sec. 4, Taipei 106 (China); Weng, J.H. [Department of Chemical and Materials Engineering, Tunghai University, Taichung 407 (China); Santhanam, R. [Solid State and Surface Sciences Lab., Department of Physics, Southern University, Baton Rouge, LA-70808 (United States); Lee, J.F.; Chen, J.M.; Liu, D.G. [National Synchrotron Radiation Research Center (NSRRC), Hsinchu (China)

    2010-03-15

    Nanostructured transition metal oxides are of great interest as a new generation of anode materials for high energy density lithium-ion batteries. In this work, research has been focused on the nano-sized (grain size {proportional_to}7 nm) CoO anode material and this material delivers charge capacity of 900 mAh g{sup -1} that exceeds the theoretical value of 715 mAh g{sup -1}. Possible reason for this unaccounted and unexplained anomalous capacity of the nano-sized CoO material has been suggested by thermogravimetric analysis. A mechanism for this interesting behavior has been systematically evaluated by using X-ray absorption spectroscopy. The anomalous capacity is proposed to be associated with the formation of oxygen-rich CoO material. The results obtained from the nano-sized CoO material have been compared with relatively larger-sized material (grain size {proportional_to}32 nm). (author)

  8. Electrodeposition of nano-sized bismuth on copper foil as electrocatalyst for reduction of CO{sub 2} to formate

    Energy Technology Data Exchange (ETDEWEB)

    Lv, Weixin; Zhou, Jing; Bei, Jingjing [School of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng, 224051 (China); Zhang, Rui, E-mail: zhangrui@ycit.cn [School of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng, 224051 (China); Wang, Lei [Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People’s Republic of China, Heilongjiang University, Harbin, 150080 (China); Xu, Qi [School of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng, 224051 (China); Wang, Wei, E-mail: wangw@ycit.edu.cn [School of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng, 224051 (China)

    2017-01-30

    Highlights: • Bi/Cu electrode was prepared by depositing nano-sized Bi catalyst on Cu foil. • The Bi/Cu electrode can reduce CO{sub 2} to formate with a low overpotential. • The energy efficiency for reduction of CO{sub 2} to formate can reach to 50%. • A Tafel slope of 128 mV decade{sup −1} was observed for producing formate. - Abstract: Electrochemical reduction of carbon dioxide (CO{sub 2}) to formate is energetically inefficient because high overpotential is required for reduction of CO{sub 2} to formate on most traditional catalysts. In this paper, a novel nano-sized Bi-based electrocatalyst deposited on a Cu foil has been synthesized, which can be used as a cathode for electrochemical reduction of CO{sub 2} to formate with a low overpotential (0.69 V) and a high selectivity (91.3%). The electrocatalyst can show excellent catalytic performance toward reduction of CO{sub 2} which can probably be attributed to the nano-sized structure and the surface oxide layer. The energy efficiency for reduction of CO{sub 2} to formate can reach to 50% when an Ir{sub x}Sn{sub y}Ru{sub z}O{sub 2}/Ti electrode is used as anode, it is one of the highest values found in the literatures and very practicable for sustainable fuel synthesis.

  9. Polyol mediated nano size zinc oxide and nanocomposites with poly(methyl methacrylate

    Directory of Open Access Journals (Sweden)

    2011-07-01

    Full Text Available Organophilic nano ZnO particles have been synthesized in various diols (ethylene glycol – EG, 1,2 propane diol – PD, 1,4 butane diol – BD and tetra(ethylene glycol – TEG in the presence of p-toluenesulfonic acid, p-TsOH, as an end capping agent. The addition of p-TsOH reduces the ZnO particle size and increases its crystallite size. With increasing diol main chain length the ZnO particle size increases (EG (32 nm < PD (33 nm < BD (72 nm < TEG (86 nm. Using the assynthesized and unmodified ZnO nanocomposites with poly(methyl methacrylate, PMMA, matrix have been prepared by the in-situ bulk polymerization of methyl methacrylate, MMA. The addition of surface modifiers is avoided which is an advantage for the application since they can influence other properties of the material. ZnO particles, especially those with smaller particle sizes (EG – 32 nm, PD – 33 nm showed enhanced effect on the thermal stability of PMMA, ultraviolet, UV, absorption and transparency for visible light. Transparent materials with high UV absorption and with enhanced resistance to sunlight were obtained by optimizing the nanocomposite preparation procedure using ZnO particles of about 30 nm size in concentrations between 0.05 and 0.1 wt%. The reported nanocomposite preparation procedure is compatible with the industrial process of PMMA sheet production.

  10. Effect of silicon carbide addition on the corrosion behavior of powder metallurgy Cu−30Zn brass in a 3.5 wt% NaCl solution

    Energy Technology Data Exchange (ETDEWEB)

    Almomani, Mohammed Ali, E-mail: maalmomani7@just.edu.jo [Department of Industrial Engineering, Jordan University of Science and Technology, P. O. Box 3030, Irbid 22110 (Jordan); Tyfour, Wa' il Radwan, E-mail: wrtyfou@just.edu.jo [Department of Industrial Engineering, Jordan University of Science and Technology, P. O. Box 3030, Irbid 22110 (Jordan); Nemrat, Mohammed Hani, E-mail: mohammednemrat@yahoo.com [Department of Mechanical Engineering, Institute of Applied Technology, Abu Dhabi (United Arab Emirates)

    2016-09-15

    A study was made to evaluate the corrosion behavior when Cu−30Zn alloy is reinforced with different weight fractions of silicon carbide (SiC) particles in a simulated sea solution (3.5 wt% NaCl aqueous solution). The composites were produced via powder metallurgy (PM) route. For the sake of comparison, the corrosion behaviors of unreinforced and reinforced alloy were examined. Electrochemical measurements (potentiodynamic testing) showed that the corrosion rate of the composites decreased with increase of SiC weight percentages, as a result of weak microgalvanic couple between reinforcement particles and Cu−30Zn matrix, and the low possibility of intermetallic phases formation. ANOVA test indicated that the variations of corrosion rate of the composites upon changing weight percentages of SiC particles are statistically significant. Polarization curves showed that the passive film tends to be less stable, and the potential difference between passivation and free corrosion points increased with increase of SiC weight percentages, as SiC cathodically protect the matrix material by sacrificial anodic dissolution of crevice regions about reinforcement particles. Scanning Electron Microscope (SEM) images of the sample's surfaces before and after testing are in agreement with the electrochemical results. - Highlights: • Effect of adding SiC on both uniform and localized corrosion of Cu−30Zn alloy is studied. • Reinforcing Cu−30Zn with nonconductive SiC particles decreases its tendency to uniform and localized corrosion. • Reinforcement particles cathodically protect the matrix material, and retard pit propagation to the matrix.

  11. Application of electron crystallography to structure characterization of ZnS nanocrystals

    Directory of Open Access Journals (Sweden)

    Jin-Gyu Kim

    2011-07-01

    Full Text Available We chracterized the structure properties of two types of ZnS nanocrystals by electron crystallography. X-ray diffraction analysis for these ZnS nanocrystals was performed to determine their initial structures. Their crystallite sizes were about 5.9 nm and 8.1 nm and their crystal systems were hexagonal and cubic, respectively. Their atomic structures, however, could not be determined because of the weak diffraction intensities as well as the unexpected intensities from impurty. To overcome these problems, the structures of ZnS nanocrystals were resolved by electron crystallography using EF-EPD (energy-filtered electron powder diffraction and HRTEM (high resolution transmission electron microscopy methods. The structrues determined by Rietveld analysis are P63mc (a = 3.8452 Å, c = 18.5453 Å and F-43m (a = 5.4356 Å, respectively. Their crystallite shapes were nanorods and quasi-nanoparticles and the nanorod crystal were grown along the [001] direction. It was revealed that the phase transformation between the cubic sphalerite to the hexagonal wurtzite structure of ZnS nanocrytals was related to their shapes and growth mechanism. Electron cryststallogrpahy, employing EF-EPD and HRTEM methods together, has advantages for structure analysis and property chracterization of nano-sized materials.

  12. Thermal shock behavior of nano-sized SiC particulate reinforced AlON composites

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, X.J. [Department of Materials Science and Engineering, School of Materials and Metallurgy, Northeastern University, Shenyang, Liaoning 110004 (China); Department of Mechanical and Industrial Engineering, Ryerson University, Toronto, Ontario M5B 2K3 (Canada); Ru, H.Q., E-mail: ruhq@smm.neu.edu.cn [Department of Materials Science and Engineering, School of Materials and Metallurgy, Northeastern University, Shenyang, Liaoning 110004 (China); Chen, D.L., E-mail: dchen@ryerson.ca [Department of Mechanical and Industrial Engineering, Ryerson University, Toronto, Ontario M5B 2K3 (Canada); Zhang, N.; Liang, B. [Key Laboratory of Advanced Materials Manufacturing Technology of Liaoning Province, Shenyang University, Shenyang, Liaoning 110044 (China)

    2012-03-25

    Highlights: Black-Right-Pointing-Pointer Addition of nano-SiC particles enhances residual strength and critical temperature. Black-Right-Pointing-Pointer Young's modulus decreases with increasing quenching temperature. Black-Right-Pointing-Pointer Linear relationship between residual strength and thermal shock times is obtained. Black-Right-Pointing-Pointer Rougher fracture surfaces in the SiC-AlON composites are observed. - Abstract: Aluminum oxynitride (AlON) has been considered as a potential ceramic material for high-performance structural and advanced refractory applications. Thermal shock resistance is a major concern and an important performance index of high-temperature ceramics. While silicon carbide (SiC) particles have been proven to improve mechanical properties of AlON ceramic, the high-temperature thermal shock behavior was unknown. The aim of this investigation was to identify the thermal shock resistance and underlying mechanisms of AlON ceramic and 8 wt% SiC-AlON composites over a temperature range between 175 Degree-Sign C and 275 Degree-Sign C. The residual strength and Young's modulus after thermal shock decreased with increasing quenching temperature and thermal shock times due to large temperature gradients and thermal stresses caused by abrupt water-quenching. A linear relationship between the residual strength and thermal shock times was observed in both pure AlON and SiC-AlON composites. The addition of nano-sized SiC particles increased both residual strength and critical temperature from 200 Degree-Sign C in the monolithic AlON to 225 Degree-Sign C in the SiC-AlON composites due to the toughening effect, the lower coefficient of thermal expansion and higher thermal conductivity of SiC. The enhancement of the thermal shock resistance in the SiC-AlON composites was directly related to the change of fracture mode from intergranular cracking along with cleavage-type fracture in the AlON to a rougher fracture surface with ridge

  13. Enhanced ductility of Mg–3Al–1Zn alloy reinforced with short length multi-walled carbon nanotubes using a powder metallurgy method

    Directory of Open Access Journals (Sweden)

    Muhammad Rashad

    2015-08-01

    Full Text Available Mg–3Al–1Zn–CNTs composites, with different weight fractions (0.25–1.0 wt% of carbon nanotubes (CNTs were successfully fabricated via a powder metallurgy method. The processing parameters were adopted in such a way to have uniform dispersion of short length CNTs without any damage, as well as refined and dissolved β phases structures throughout the composite matrix. The composite exhibited impressive increase in microhardness (about +23% and tensile failure strain value (about +98% without significant compromise in tensile strength, compared to the un-reinforced Mg–3Al–1Zn alloy. The synthesized composites can be used in automotive and aerospace industries due to their low density and high specific strength.

  14. Particle phase distribution of polycyclic aromatic hydrocarbons in stormwater — Using humic acid and iron nano-sized colloids as test particles

    DEFF Research Database (Denmark)

    Nielsen, Katrine; Kalmykova, Yuliya; Strömvall, Ann-Margret

    2015-01-01

    The distribution of polycyclic aromatic hydrocarbons (PAHs) in different particulate fractions in stormwater: Total, Particulate, Filtrated, Colloidal and Dissolved fractions, were examined and compared to synthetic suspensions of humic acid colloids and iron nano-sized particles. The distribution...

  15. Influence of high-pressure torsion on formation/destruction of nano-sized spinodal structures

    Science.gov (United States)

    Alhamidi, Ali; Edalati, Kaveh; Horita, Zenji

    2018-04-01

    The microstructures and hardness of Al - 30 mol.% Zn are investigated after processing by high-pressure torsion (HPT) for different numbers of revolutions, N = 1, 3, 10 or 25, as well as after post-HPT annealing at different temperatures, T = 373 K, 473 K, 573 K and 673 K. It was found that a work softening occurs by decreasing the grain size to the submicrometer level and increasing the fraction of high-angle boundaries. As a result of HPT processing, a complete decomposition of supersaturated solid solution of Zn in Al occurs and the spinodal structure is destroyed. This suggests that softening of the Al-Zn alloys after HPT is due to the decomposition of the supersaturated solid solution and destruction of spinodal decomposition. After post-HPT annealing, ultrafine-grained Al-Zn alloys show an unusual mechanical properties and its hardness increased to 187 HV. Microstructural analysis showed that the high hardness after post-HPT annealing is due to the formation of spinodal structures.

  16. Investigation of structural and magnetic properties of Ni0.5Zn0.5Fe2O4 nano powders prepared by self combustion method

    International Nuclear Information System (INIS)

    Sudheesh, V.D.; Nehra, J.; Vinesh, A.; Sebastian, V.; Lakshmi, N.; Dutta, Dimple P.; Reddy, V.R.; Venugopalan, K.; Gupta, Ajay

    2013-01-01

    Graphical abstract: Display Omitted Highlights: ► Ni 0.5 Zn 0.5 Fe 2 O 4 prepared by self combustion with uniform/nonuniform heating. ► Characterized using TEM, XRD, in-field Mössbauer and DC magnetometry. ► Leads to bimodal (S1) and very narrow size distribution (S2) type nano samples. ► S1 has magnetic properties of bulk Ni 0.5 Zn 0.5 Fe 2 O 4 . ► Although very even sized, S2 large magnetic anisotropy distribution. -- Abstract: Nano powders of Ni 0.5 Zn 0.5 Fe 2 O 4 have been synthesized by the self-combustion method at a relatively low temperature of 473 K under conditions of non-uniform and uniform heating. Rietveld fitting of X-ray diffractograms confirm the formation of the pure spinel phase in both samples. Transmission electron microscopy indicates that the sample prepared under non-uniform heating has a bimodal particle size distribution (average values 16 nm and 6 nm) while the one prepared under uniform heating has a very narrow particle size distribution (average size 4 nm). Low temperature, in-field Mössbauer spectroscopic studies clearly show surface spin contributions. The hyperfine fields and Curie temperature of the non-uniformly heated sample are in good agreement with those reported for the corresponding bulk samples. Despite having a very narrow particle size distribution, the uniformly heated sample has a large anisotropy distribution which is evident in the broad transition visible in the temperature dependent magnetization curve. It is also corroborated by the fact that the experimental magnetization curve at room temperature requires two Langevin functions for satisfactory reproduction.

  17. Development of nano-sized α-Al2O3:C films for application in digital radiology

    International Nuclear Information System (INIS)

    Silva, Edna C.

    2011-01-01

    Ceramic materials are widely used as sensors for ionizing radiation. In nuclear applications, the alpha-alumina doped with carbon (α-Al 2 O 3 :C) is the most widely ceramic used because of its excellent optically stimulated luminescence (OSL) and thermoluminescent (TL) properties applied to detection of ionizing radiation. Another application of OSL and TL materials are in Digital Radiography, with ceramic/polymeric film composites. Recently, Computed Radiography (CR) devices based on OSL materials are replacing the old conventional film radiography. In this study we investigate the thermoluminescence of nano-sized α-Al 2 O 3 samples doped with different percentages of carbon, sintered in reducing atmospheres at temperatures ranging from 1300 to 1750 deg C. The results indicate that the nano-sized α-Al 2 O 3 :C materials have a luminescent response that could be due to both OSL and RPL properties, but without application to radiation dosimetry. Moreover, the results indicate that micro-sized α-Al 2 O 3 :C, doped with 0.5% carbon, and nano-sized ones doped with 2% of carbon, present thermoluminescent signal around 30 to 100 times the TL output signal of commercial TLD-100, the most used TL dosimeter in the world. The results indicate that these ceramic nano-particles have great potential for use in Digital Radiography based on thermoluminescent film imaging, being able to provide image resolutions much higher than the micro-sized α-Al 2 O 3 :C, in view of their improved resolution provided by nano-particulates. (author)

  18. Novel processing of bioglass ceramics from silicone resins containing micro- and nano-sized oxide particle fillers.

    Science.gov (United States)

    Fiocco, L; Bernardo, E; Colombo, P; Cacciotti, I; Bianco, A; Bellucci, D; Sola, A; Cannillo, V

    2014-08-01

    Highly porous scaffolds with composition similar to those of 45S5 and 58S bioglasses were successfully produced by an innovative processing method based on preceramic polymers containing micro- and nano-sized fillers. Silica from the decomposition of the silicone resins reacted with the oxides deriving from the fillers, yielding glass ceramic components after heating at 1000°C. Despite the limited mechanical strength, the obtained samples possessed suitable porous architecture and promising biocompatibility and bioactivity characteristics, as testified by preliminary in vitro tests. © 2013 Wiley Periodicals, Inc.

  19. Thermoelectric properties of In{sub 0.2}Co{sub 4}Sb{sub 12} skutterudites with embedded PbTe or ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Chubilleau, C.; Lenoir, B.; Candolfi, C.; Masschelein, P. [Université de Lorraine, CNRS, UMR 7198, Institut Jean Lamour, Parc de Saurupt, 54011 Nancy (France); Dauscher, A., E-mail: anne.dauscher@univ-lorraine.fr [Université de Lorraine, CNRS, UMR 7198, Institut Jean Lamour, Parc de Saurupt, 54011 Nancy (France); Guilmeau, E. [Laboratoire CRISMAT, UMR 6508, 6 boulevard Maréchal Juin, 14050 Caen Cedex (France); Godart, C. [ICMPE-CMTR, CNRS-UMR 7182, 2-8 rue H. Dunant, 94320 Thiais (France)

    2014-03-15

    Highlights: • Fabrication of nanostructured skutterudites ZnO or PbTe/In{sub 0.2}Co{sub 4}Sb{sub 12.} • Thermal conductivity modeling accounts for experimental results. • Greater lattice thermal conductivity decrease in In{sub 0.2}Co{sub 4}Sb{sub 12} than in CoSb{sub 3}. • A max ZT of 1.05 is obtained at 700 K in a 2 wt% ZnO-containing sample. -- Abstract: Transport properties of the skutterudite compound In{sub 0.2}Co{sub 4}Sb{sub 12} containing ZnO or PbTe nano-sized particles (2–12 wt%) were investigated by means of electrical resistivity, thermopower and thermal conductivity between 5 and 800 K. The composite powders were prepared by freeze-drying the nanoparticles with micron-sized In{sub 0.2}Co{sub 4}Sb{sub 12} powders. Densification was achieved by spark plasma sintering. All composites were characterized by X-ray powder diffraction and scanning electron microscopy. All the transport coefficients show similar temperature dependences suggesting little influence of the nature, semiconducting or insulating, of the nanoparticles. Both the electrical and the thermal conductivities decrease with increasing the PbTe or ZnO content. The impact of ZnO and PbTe on the thermal conductivity was modelled based on the Debye model taking into account a relaxation time constant reflecting phonon scattering by spherical nanoparticles. A maximum dimensionless figure of merit ZT of 1.05 at 700 K was achieved in a sample containing 2 wt% ZnO, a value quite similar to that of the reference In{sub 0.2}Co{sub 4}Sb{sub 12} compound.

  20. Responses of human cells to ZnO nanoparticles: a gene transcription study†

    Science.gov (United States)

    Moos, Philip J.; Olszewski, Kyle; Honeggar, Matthew; Cassidy, Pamela; Leachman, Sancy; Woessner, David; Cutler, N. Shane; Veranth, John M.

    2013-01-01

    The gene transcript profile responses to metal oxide nanoparticles was studied using human cell lines derived from the colon and skin tumors. Much of the research on nanoparticle toxicology has focused on models of inhalation and intact skin exposure, and effects of ingestion exposure and application to diseased skin are relatively unknown. Powders of nominally nanosized SiO2, TiO2, ZnO and Fe2O3 were chosen because these substances are widely used in consumer products. The four oxides were evaluated using colon-derived cell lines, RKO and CaCo-2, and ZnO and TiO2 were evaluated further using skin-derived cell lines HaCaT and SK Mel-28. ZnO induced the most notable gene transcription changes, even though this material was applied at the lowest concentration. Nano-sized and conventional ZnO induced similar responses suggesting common mechanisms of action. The results showed neither a non-specific response pattern common to all substances nor synergy of the particles with TNF-α cotreatment. The response to ZnO was not consistent with a pronounced proinflammatory signature, but involved changes in metal metabolism, chaperonin proteins, and protein folding genes. This response was observed in all cell lines when ZnO was in contact with the human cells. When the cells were exposed to soluble Zn, the genes involved in metal metabolism were induced but the genes involved in protein refoldling were unaffected. This provides some of the first data on the effects of commercial metal oxide nanoparticles on human colon-derived and skin-derived cells. PMID:21769377

  1. Nano-sized Fe2O3/Fe3O4 facilitate anaerobic transformation of hexavalent chromium in soil-water systems.

    Science.gov (United States)

    Zhang, Yaxian; Li, Hua; Gong, Libo; Dong, Guowen; Shen, Liang; Wang, Yuanpeng; Li, Qingbiao

    2017-07-01

    The purpose of this study is to investigate the effects of nano-sized or submicro Fe 2 O 3 /Fe 3 O 4 on the bioreduction of hexavalent chromium (Cr(VI)) and to evaluate the effects of nano-sized Fe 2 O 3 /Fe 3 O 4 on the microbial communities from the anaerobic flooding soil. The results indicated that the net decreases upon Cr(VI) concentration from biotic soil samples amended with nano-sized Fe 2 O 3 (317.1±2.1mg/L) and Fe 3 O 4 (324.0±22.2mg/L) within 21days, which were approximately 2-fold of Cr(VI) concentration released from blank control assays (117.1±5.6mg/L). Furthermore, the results of denaturing gradient gel electrophoresis (DGGE) and high-throughput sequencing indicated a greater variety of microbes within the microbial community in amendments with nano-sized Fe 2 O 3 /Fe 3 O 4 than the control assays. Especially, Proteobacteria occupied a predominant status on the phylum level within the indigenous microbial communities from chromium-contaminated soils. Besides, some partial decrease of soluble Cr(VI) in abiotic nano-sized Fe 2 O 3 /Fe 3 O 4 amendments was responsible for the adsorption of nano-sized Fe 2 O 3 /Fe 3 O 4 to soluble Cr(VI). Hence, the presence of nano-sized Fe 2 O 3 /Fe 3 O 4 could largely facilitate the mobilization and biotransformation of Cr(VI) from flooding soils by adsorption and bio-mediated processes. Copyright © 2017. Published by Elsevier B.V.

  2. Synthesis and electrochemical performance of surface-modified nano-sized core/shell tin particles for lithium ion batteries

    International Nuclear Information System (INIS)

    Schmuelling, Guido; Meyer, Hinrich-Wilhelm; Placke, Tobias; Winter, Martin; Oehl, Nikolas; Knipper, Martin; Kolny-Olesiak, Joanna; Plaggenborg, Thorsten; Parisi, Jürgen

    2014-01-01

    Tin is able to lithiate and delithiate reversibly with a high theoretical specific capacity, which makes it a promising candidate to supersede graphite as the state-of-the-art negative electrode material in lithium ion battery technology. Nevertheless, it still suffers from poor cycling stability and high irreversible capacities. In this contribution, we show the synthesis of three different nano-sized core/shell-type particles with crystalline tin cores and different amorphous surface shells consisting of SnO x and organic polymers. The spherical size and the surface shell can be tailored by adjusting the synthesis temperature and the polymer reagents in the synthesis, respectively. We determine the influence of the surface modifications with respect to the electrochemical performance and characterize the morphology, structure, and thermal properties of the nano-sized tin particles by means of high-resolution transmission electron microscopy, x-ray diffraction, and thermogravimetric analysis. The electrochemical performance is investigated by constant current charge/discharge cycling as well as cyclic voltammetry. (paper)

  3. Hierarchically structured superhydrophobic coatings fabricated by successive Langmuir-Blodgett deposition of micro-/nano-sized particles and surface silanization.

    Science.gov (United States)

    Tsai, Ping-Szu; Yang, Yu-Min; Lee, Yuh-Lang

    2007-11-21

    The present study demonstrates the creation of a stable, superhydrophobic surface by coupling of successive Langmuir-Blodgett (LB) depositions of micro- and nano-sized (1.5 µm/50 nm, 1.0 µm/50 nm, and 0.5 µm/50 nm) silica particles on a glass substrate with the formation of a self-assembled monolayer of dodecyltrichlorosilane on the surface of the particulate film. Particulate films, in which one layer of 50 nm particles was deposited over one to five sublayers of larger micro-sized particles, with hierarchical surface roughness and superhydrophobicity, were successfully fabricated. Furthermore, the present 'two-scale' (micro- and nano-sized particles) approach is superior to the previous 'one-scale' (micro-sized particles) approach in that both higher advancing contact angle and lower contact angle hysteresis can be realized. Experimental results revealed that the superhydrophobicity exhibited by as-fabricated particulate films with different sublayer particle diameters increases in the order of 0.5 µm>1.0 µm>1.5 µm. However, no clear trend between sublayer number and surface superhydrophobicity could be discerned. An explanation of superhydrophobicity based on the surface roughness introduced by two-scale particles is also proposed.

  4. Fabrication of nano-sized magnetic tunnel junctions using lift-off process assisted by atomic force probe tip.

    Science.gov (United States)

    Jung, Ku Youl; Min, Byoung-Chul; Ahn, Chiyui; Choi, Gyung-Min; Shin, Il-Jae; Park, Seung-Young; Rhie, Kungwon; Shin, Kyung-Ho

    2013-09-01

    We present a fabrication method for nano-scale magnetic tunnel junctions (MTJs), employing e-beam lithography and lift-off process assisted by the probe tip of atomic force microscope (AFM). It is challenging to fabricate nano-sized MTJs on small substrates because it is difficult to use chemical mechanical planarization (CMP) process. The AFM-assisted lift-off process enables us to fabricate nano-sized MTJs on small substrates (12.5 mm x 12.5 mm) without CMP process. The e-beam patterning has been done using bi-layer resist, the poly methyl methacrylate (PMMA)/ hydrogen silsesquioxane (HSQ). The PMMA/HSQ resist patterns are used for both the etch mask for ion milling and the self-aligned mask for top contact formation after passivation. The self-aligned mask buried inside a passivation oxide layer, is readily lifted-off by the force exerted by the probe tip. The nano-MTJs (160 nm x 90 nm) fabricated by this method show clear current-induced magnetization switching with a reasonable TMR and critical switching current density.

  5. Microstructures and Tensile Properties of Al–Cu Matrix Composites Reinforced with Nano-Sized SiCp Fabricated by Semisolid Stirring Process

    Directory of Open Access Journals (Sweden)

    Feng Qiu

    2017-02-01

    Full Text Available The nano-sized SiCp/Al–Cu composites were successfully fabricated by combining semisolid stirring with ball milling technology. Microstructures were examined by an olympus optical microscope (OM, field emission scanning electron microscope (FESEM and transmission electron microscope (TEM. Tensile properties were studied at room temperature. The results show that the α-Al dendrites of the composites were strongly refined, especially in the composite with 3 wt. % nano-sized SiCp, of which the morphology of the α-Al changes from 200 μm dendritic crystal to 90 μm much finer equiaxial grain. The strength and ductility of the composites are improved synchronously with the addition of nano-sized SiCp particles. The as-cast 3 wt. % nano-sized SiCp/Al–Cu composite displays the best tensile properties, i.e., the yield strength, ultimate tensile strength (UTS and fracture strain increase from 175 MPa, 310 MPa and 4.1% of the as-cast Al–Cu alloy to 220 MPa, 410 MPa and 6.3%, respectively. The significant improvement in the tensile properties of the composites is mainly due to the refinement of the α-Al dendrites, nano-sized SiCp strengthening, and good interface combination between the SiCp and Al–Cu alloys.

  6. High damping Al-Fe-Mo-Si/Zn-Al composites produced by rapidly solidified powder metallurgy process

    International Nuclear Information System (INIS)

    Li, P.Y.; Dai, S.L.; Chai, S.C.; Li, Y.R.

    2000-01-01

    The metallic materials commonly used in aircraft and aerospace fields, such as aluminum and titanium alloys, steels, etc., show extremely low damping capacity (usually of the order of or less than 10 -3 ). Thus, some problems related to vibration may emerge and influence the reliability, safety and life of airplanes, satellites, etc. It has been reported that almost two thirds of errors for rockets and satellites are related to vibration and noise. One effective way to solve these vibration-related problems is to adopt high damping metallic materials. Conventional high damping alloys exhibit damping capacity above 10 -2 , however, their densities are usually great than 5 x 10 3 kg m -3 , or their strengths are less than 200 MPa (for alloys based on dislocation damping), making them impossible to be applied to aircraft and aerospace areas. Recently, some low-density high-damping metal/metal composites based on aluminum and high damping alloys have been developed in Beijing Institute of Aeronautical Materials (BIAM) by the rapidly solidified power metallurgy process. This paper aims to report the properties of the composites based on a high temperature Al-Fe-Mo-Si alloy and a high damping Zn-Al alloy, and compare them with that of 2618-T61 alloy produced by the ingot metallurgy process

  7. Enhancement of reactivity in Li4SiO4-based sorbents from the nano-sized rice husk ash for high-temperature CO2 capture

    International Nuclear Information System (INIS)

    Wang, Ke; Zhao, Pengfei; Guo, Xin; Li, Yimin; Han, Dongtai; Chao, Yang

    2014-01-01

    Highlights: • The Li 4 SiO 4 sorbent from nano-sized rice husk ash was prepared and characterized. • The Aerosil and Quartz were comparably used for synthesized Li 4 SiO 4 . • The structure of sorbent was depended on the morphology of heated silicon materials. • The pretreatment sorbent showed increase in the CO 2 uptake and kinetic behavior. • This promising sorbent also maintained higher capacities during the multiple cycles. - Abstract: Using the cost-effective, renewable and nano-sized of citric acid pretreatment rice husk ash (CRHA) as silicon source, high efficient Li 4 SiO 4 (lithium orthosilicate)-based sorbents (CRHA-Li 4 SiO 4 ) for high-temperature CO 2 capture were prepared through the solid-state reaction at lower temperature (700 °C). Two typical raw materials (nano-structured Aerosil and crystalline Quartz powders) were used to synthesize Li 4 SiO 4 sorbents (Aerosil-Li 4 SiO 4 and Quartz-Li 4 SiO 4 ) for comparison purposes. The phase composition behavior, surface area, and morphology of the silicon sources, heat treated raw materials and as-received Li 4 SiO 4 sorbents were studied by analytical techniques. The CO 2 adsorption capacity and adsorption–desorption performance were tested by the thermo-gravimetric analyses (CO 2 atmosphere) and a fixed bed reactor, respectively. Compared with the case of its original samples, the morphology of heat treated raw materials had a greater effect on the phase composition, microstructure, special surface area and CO 2 adsorption properties of their resulting sorbents. Although the calcined Quartz sample maintained the structure of micron particles, its reactivity was not enough to react completely with Li 2 CO 3 . Due to the greater reactivity of nanoparticles, Aerosil-Li 4 SiO 4 presented pure of Li 4 SiO 4 whereas it obtained large particles with dense morphology, which was coming from the pronounced fusing of silica nanoparticles during the calcined process. Conversely, CRHA-Li 4 SiO 4

  8. Thermoelectrical and thermal analyses of copper(II) acetate monohydrate ZnO-matrix composite powder obtained by freeze-drying

    International Nuclear Information System (INIS)

    Bellini, Jusmar Valentin; Pineda, Edgardo Alfonso Gomez; Rocha, Raquel de Almeida; Ponzoni, Andre Luis de Lima; Paesano, Andrea

    2006-01-01

    The thermal history of freeze-dried mixtures of composite powders containing ZnO-matrix and (CH 3 COO) 2 Cu.H 2 O (copper(II) acetate monohydrate) was undertaken by thermal analysis (TA) coupled to thermoelectrical analysis (TEA). Experiments were carried out on compacted samples, under non-isothermal conditions, in air, up to 350 deg. C, by measuring the electrical resistance during heating, called thermoelectrical resistometry (TER), and by differential scanning calorimetry (DSC). Activation energy (E a ) for exothermal events related to the decomposition of (CH 3 COO) 2 Cu (copper(II) acetate, CuAc 2 ), observed within the range 225-325 deg. C, was estimated according to ASTM E 698 method. Values of E a equal to 154 and 155 kJ/mol were obtained by TER and DSC, respectively. TER showed that the thermal decomposition of CuAc 2 involves the liberation of electrons. Results also indicated that TER may be used as an alternative or complementary method for the study of the thermal decomposition mechanisms of transition metal(II) acetates

  9. Nervous System Injury in Response to Contact With Environmental, Engineered and Planetary Micro- and Nano-Sized Particles

    Directory of Open Access Journals (Sweden)

    Tatiana Borisova

    2018-06-01

    Full Text Available Nerve cells take a special place among other cells in organisms because of their unique function mechanism. The plasma membrane of nerve cells from the one hand performs a classical barrier function, thereby being foremost targeted during contact with micro- and nano-sized particles, and from the other hand it is very intensively involved in nerve signal transmission, i.e., depolarization-induced calcium-dependent compound exocytosis realized via vesicle fusion following by their retrieval and calcium-independent permanent neurotransmitter turnover via plasma membrane neurotransmitter transporters that utilize Na+/K+ electrochemical gradient as a driving force. Worldwide traveling air pollution particulate matter is now considered as a possible trigger factor for the development of a variety of neuropathologies. Micro- and nano-sized particles can reach the central nervous system during inhalation avoiding the blood–brain barrier, thereby making synaptic neurotransmission extremely sensitive to their influence. Neurosafety of environmental, engineered and planetary particles is difficult to predict because they possess other features as compared to bulk materials from which the particles are composed of. The capability of the particles to absorb heavy metals and organic neurotoxic molecules from the environment, and moreover, spontaneously interact with proteins and lipids in organisms and form biomolecular corona can considerably change the particles‘ features. The absorption capability occasionally makes them worldwide traveling particulate carriers for delivery of environmental neurotoxic compounds to the brain. Discrepancy of the experimental data on neurotoxicity assessment of micro- and nano-sized particles can be associated with a variability of systems, in which neurotoxicity was analyzed and where protein components of the incubation media forming particle biocorona can significantly distort and even eliminate factual particle

  10. Propagation of electro-kinetic waves in magnetized GaN semiconductor with nano-sized ion colloids

    Energy Technology Data Exchange (ETDEWEB)

    Saxena, Ajay [Government College, Garoth, Dist. Mandsaur (M P) (India); Sharma, Giriraj, E-mail: grsharma@gmail.com [SRJ Government Girls’ College, Neemuch (M P) (India); Jat, K. L. [Swami Vivekanand Government P G College, Neemuch (M P) (India); Rishi, M. P. [Shahid Bhagat Singh Government P G College, Jaora, Dist Ratlam (M P) (India)

    2015-07-31

    Based on hydrodynamic model of multi-component plasma, an analytical study on propagation of longitudinal electro-kinetic (LEK) waves in wurtzite and zincblende structures of GaN is carried out. Nano-sized ion colloids (NICs) are embedded in the sample by the technique of ion-implantation. The implanted NICs are considered massive by an order as compared to the host lattice points and do not participate in Based LEK perturbations. Though, the NICs are continuously bombarded by the electrons as well as the holes yet, the former acquires a net negative charge owing to relatively higher mobility of electrons and consequently results into depletion of electron density in the medium. It i s found that the presence of charged NICs significantly modifies the dispersion and amplification characteristics of LEK waves in magnetized GaN semiconductor plasma and their role becomes increasingly effective as the fraction of charge on them increases.

  11. Propagation of electro-kinetic waves in magnetized GaN semiconductor with nano-sized ion colloids

    International Nuclear Information System (INIS)

    Saxena, Ajay; Sharma, Giriraj; Jat, K. L.; Rishi, M. P.

    2015-01-01

    Based on hydrodynamic model of multi-component plasma, an analytical study on propagation of longitudinal electro-kinetic (LEK) waves in wurtzite and zincblende structures of GaN is carried out. Nano-sized ion colloids (NICs) are embedded in the sample by the technique of ion-implantation. The implanted NICs are considered massive by an order as compared to the host lattice points and do not participate in Based LEK perturbations. Though, the NICs are continuously bombarded by the electrons as well as the holes yet, the former acquires a net negative charge owing to relatively higher mobility of electrons and consequently results into depletion of electron density in the medium. It i s found that the presence of charged NICs significantly modifies the dispersion and amplification characteristics of LEK waves in magnetized GaN semiconductor plasma and their role becomes increasingly effective as the fraction of charge on them increases

  12. Phase constitution and interface structure of nano-sized Ag-Cu/AlN multilayers: Experiment and ab initio modeling

    Energy Technology Data Exchange (ETDEWEB)

    Pigozzi, Giancarlo; Janczak-Rusch, Jolanta; Passerone, Daniele; Antonio Pignedoli, Carlo; Patscheider, Joerg; Jeurgens, Lars P. H. [Empa, Swiss Federal Laboratories for Materials Science and Technology, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland); Antusek, Andrej [Empa, Swiss Federal Laboratories for Materials Science and Technology, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland); Faculty of Materials Science and Technology, Slovak University of Technology in Bratislava, Paulinska 16, 917 24 Trnava (Slovakia); Parlinska-Wojtan, Magdalena [Empa, Swiss Federal Laboratories for Materials Science and Technology, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland); University of Rzeszow, Institute of Physics, ul. Rejtana 16a, 35-959 Rzeszow (Poland); Bissig, Vinzenz [Kirsten Soldering AG, Hinterbergstrasse 32, CH-6330 Cham (Switzerland)

    2012-10-29

    Nano-sized Ag-Cu{sub 8nm}/AlN{sub 10nm} multilayers were deposited by reactive DC sputtering on {alpha}-Al{sub 2}O{sub 3}(0001) substrates. Investigation of the phase constitution and interface structure of the multilayers evidences a phase separation of the alloy sublayers into nanosized grains of Ag and Cu. The interfaces between the Ag grains and the quasi-single-crystalline AlN sublayers are semi-coherent, whereas the corresponding Cu/AlN interfaces are incoherent. The orientation relationship between Ag and AlN is constant throughout the entire multilayer stack. These observations are consistent with atomistic models of the interfaces as obtained by ab initio calculations.

  13. Understanding dual precipitation strengthening in ultra-high strength low carbon steel containing nano-sized copper precipitates and carbides

    Science.gov (United States)

    Phaniraj, M. P.; Shin, Young-Min; Jung, Woo-Sang; Kim, Man-Ho; Choi, In-Suk

    2017-07-01

    Low carbon ferritic steel alloyed with Ti, Mo and Cu was hot rolled and interrupt cooled to produce nano-sized precipitates of copper and (Ti,Mo)C carbides. The steel had a tensile strength of 840 MPa, an increase in yield strength of 380 MPa over that of the plain carbon steel and reasonable ductility. Transmission electron microscopy and small angle neutron scattering were used to characterize size and volume fraction of the precipitates in the steels designed to form only copper precipitates and only (Ti,Mo)C carbides. The individual and combined precipitation strengthening contributions was calculated using the size and volume fraction of precipitates and compared with the measured values.

  14. Adhesion of nano-sized particles to the surface of bacteria: mechanistic study with the extended DLVO theory.

    Science.gov (United States)

    Hwang, Geelsu; Ahn, Ik-Sung; Mhin, Byung Jin; Kim, Ju-Young

    2012-09-01

    Due to the increasing production and application of nanoparticles, their release into the environment would be inevitable, which requires a better understanding of their fate in the environment. When considering their toxic behavior or biodegradation as their fate, their adhesion to the cell surface must be the first step to be thoroughly studied. In this study, nano-sized polymeric particles of urethane acrylate with various hydrophobicity and ionic properties were synthesized as model nanoparticles, and their adhesion to Pseudomonas putida strains was monitored. The higher hydrophobicity and positive charge density on the particle surface exhibited the larger adhesion to the bacteria, whereas negative charge density on the particle hindered their adhesion to the bacteria, albeit high hydrophobicity of particle. These observations were successfully explained with the extended Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. Copyright © 2012 Elsevier B.V. All rights reserved.

  15. Preparation of nano-sized {alpha}-Al{sub 2}O{sub 3} from oil shale ash

    Energy Technology Data Exchange (ETDEWEB)

    An, Baichao; Wang, Wenying; Ji, Guijuan; Gan, Shucai; Gao, Guimei; Xu, Jijing; Li, Guanghuan [College of Chemistry, Jilin University, Changchun 130026 (China)

    2010-01-15

    Oil shale ash (OSA), the residue of oil shale semi-coke roasting, was used as a raw material to synthesize nano-sized {alpha}-Al{sub 2}O{sub 3}. Ultrasonic oscillation pretreatment followed by azeotropic distillation was employed for reducing the particle size of {alpha}-Al{sub 2}O{sub 3}. The structural characterization at molecular and nanometer scales was performed using X-ray diffraction (XRD), transmission electron microscopy (TEM), respectively. The interaction between alumina and n-butanol was characterized by Fourier transform infrared spectroscopy (FT-IR). The results revealed that the crystalline phase of alumina nanoparticles was regular and the well dispersed alumina nanoparticles had a diameter of 50-80 nm. In addition, the significant factors including injection rate of carbon oxide (CO{sub 2}), ultrasonic oscillations, azeotropic distillation and surfactant were investigated with respect to their effects on the size of the alumina particles. (author)

  16. Nano-sized surface modifications induced by the impact of slow highly charged ions - A first review

    International Nuclear Information System (INIS)

    Aumayr, F.; El-Said, A.S.; Meissl, W.

    2008-01-01

    Irradiation of crystalline solid targets with swift heavy ions can lead to the formation of latent tracks in the solid and the creation of (mostly-hillock type) nanostructures on the surface. Recently similar surface modifications with nanometer dimensions have been demonstrated for the impact of individual, very slow but highly charged ions on various surfaces. We will review the current state of this new field of research. In particular we will discuss the circumstances and conditions under which nano-sized features (hillocks or craters) on different surfaces due to impact of slow highly charged ions can be produced. The use of slow highly charged ions instead of swift heavy ions might be of considerable interest for some practical applications

  17. Thermal conductivity enhancement and sedimentation reduction of magnetorheological fluids with nano-sized Cu and Al additives

    Science.gov (United States)

    Rahim, M. S. A.; Ismail, I.; Choi, S. B.; Azmi, W. H.; Aqida, S. N.

    2017-11-01

    This work presents enhanced material characteristics of smart magnetorheological (MR) fluids by utilizing nano-sized metal particles. Especially, enhancement of thermal conductivity and reduction of sedimentation rate of MR fluids those are crucial properties for applications of MR fluids are focussed. In order to achieve this goal, a series of MR fluid samples are prepared using carbonyl iron particles (CIP) and hydraulic oil, and adding nano-sized particles of copper (Cu), aluminium (Al), and fumed silica (SiO2). Subsequently, the thermal conductivity is measured by the thermal property analyser and the sedimentation of MR fluids is measured using glass tubes without any excitation for a long time. The measured thermal conductivity is then compared with theoretical models such as Maxwell model at various CIP concentrations. In addition, in order to show the effectiveness of MR fluids synthesized in this work, the thermal conductivity of MRF-132DG which is commercially available is measured and compared with those of the prepared samples. It is observed that the thermal conductivity of the samples is much better than MRF-132DG showing the 148% increment with 40 vol% of the magnetic particles. It is also observed that the sedimentation rate of the prepared MR fluid samples is less than that of MRF-132DG showing 9% reduction with 40 vol% of the magnetic particles. The mixture optimized sample with high conductivity and low sedimentation was also obtained. The magnetization of the sample recorded an enhancement of 70.5% when compared to MRF-132DG. Furthermore, the shear yield stress of the sample were also increased with and without the influence of magnetic field.

  18. Effects of calcination temperature on phase formation and particle size of Zn{sub 2}Nb{sub 34}O{sub 87} powder synthesized by solid-state reaction

    Energy Technology Data Exchange (ETDEWEB)

    Amonpattaratkit, Penphitcha, E-mail: p.amonpattaratkit@gmail.com [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Ananta, Supon, E-mail: suponananta@yahoo.com [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand)

    2013-05-15

    The solid-state mixed oxide method via a rapid vibro-milling technique was explored for the preparation of single-phase Zn{sub 2}Nb{sub 34}O{sub 87} nanopowders. Phase formation of zinc niobate was investigated as a function of calcination temperature by using a combination of thermogravimetric/differential thermal analyzer (TG/DTA) and X-ray diffraction (XRD) techniques. Morphology, particle size and chemical composition of the powders were determined by scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) technique. The obtained results clearly revealed the influences of calcination temperature on phase formation and particle size of Zn{sub 2}Nb{sub 34}O{sub 87} nanopowder. - Highlights: ► Single phase Zn{sub 2}Nb{sub 34}O{sub 87} was firstly prepared by solid-state mixed oxide method via a rapid vibro-milling technique. ► The influences of calcination temperature on phase formation and particle size were investigated. ► Zn{sub 2}Nb{sub 34}O{sub 87} powders were characterized by TG–DTA, XRD, SEM and EDX.

  19. Partial substitution of Zn Effects on the Structural and Electrical Properties of High Temperature Hg0.95Ag0.05Ba2Ca2Cu3O8+δ Superconductors

    Science.gov (United States)

    Abed, Noor S.; Fathi, Sabah J.; Jassim, Kareem A.; Mahdi, Shatha H.

    2018-05-01

    The effect of the Ag partial substitution at Hg site in HgOδ layer and Zn partial substitution at Ca site in CaO layer on the structure,Tc,electrical properties, and oxygen content for Hg-1223 have been studied. Bulk polycrystalline Hg1-xAgxBa2Ca2-yZnyCu3O8+δ compound samples with x=0.05 and y=0.0, 0.05, 0.1, 0.15, 0.2, 0.25, and 0.3, are synthesized by a solid state reaction process. Structural properties are studied by using X-ray powder pattern, the high temperature phase superconductor (Hg-1223) of the tetragonal structure didn't change with the partial substitution of Zn and Ag ions, lattice parameters c,c/a are established to vary with Ag and Zn- substitution. The surface morphology has been studied by using atomic force microscopes (AFM), showed that all specimens have good crystalline and homogeneous surface. Also give a best nano size value is 75.72 nm at x=0.05 and y=0.3. Four probe technique is used to measure Tc. The Tc were found to be increases from 129 K to 147 K and oxygen content were found to be increases with increasing Zn. In addition, dielectric properties (dielectric constant, dielectric loss factor, and the alternating electrical conductivity) are characterized directly by relating with Ag and Zn concentration.

  20. Effect of Zn on the structural and electrical properties of high temperature HgBa2Ca2Cu3O8+δ superconductor

    Science.gov (United States)

    Omar, Bilal A.; Fathi, Sabah J.; Jassim, Kareem A.

    2018-05-01

    Bulk polycrystalline HgBa2Ca2-yZnyCu3O8+δ compound samples with y =0.0, 0.05, 0.1, 0.15, 0.2, 0.25, and 0.3, are synthesized by a solid state reaction process. Study identifies Zinc partial substitution on superconductivity behavior. Structural properties are studied by using X-ray powder pattern, the high temperature phase superconductor (Hg-1223) of the tetragonal structure didn't change with the partial substitution of Zn ions in Ca site, lattice parameters c, c/a are established to vary Zn-substitution. The surface morphology has been studied by using atomic force microscopes (AFM), showed that all specimens have good crystalline and homogeneous surface. Also give a best nano size value is 83.29 nm at y=0.05. Four probe technique is used to measure Tc. The highest Tc and oxygen content were found to be Tc=132 K for y=0.05 after that, Tc decreases from 132 K to 115 K with increasing Zn. In addition, dielectric properties (dielectric constant, dielectric loss factor, and the alternating electrical conductivity) are characterized directly by relating with Zn concentration.

  1. Nanocrystalline spinel ferrite (MFe{sub 2}O{sub 4}, M = Ni, Co, Mn, Mg, Zn) powders prepared by a simple aloe vera plant-extracted solution hydrothermal route

    Energy Technology Data Exchange (ETDEWEB)

    Phumying, Santi; Labuayai, Sarawuth; Swatsitang, Ekaphan; Amornkitbamrung, Vittaya [Department of Physics, Faculty of Science, Khon Kaen University, Khon Kaen 40002 (Thailand); Integrated Nanotechnology Research Center (INRC), Khon Kaen University, Khon Kaen 40002 (Thailand); Maensiri, Santi, E-mail: santimaensiri@gmail.com [School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand)

    2013-06-01

    Graphical abstract: This figure shows the specific magnetization curves of the as-prepared MFe{sub 2}O{sub 4} (M = Ni, Co, Mn, Mg, Zn) powders obtained from room temperature VSM measurement. These curves are typical for a soft magnetic material and indicate hysteresis ferromagnetism in the field ranges of ±500 Oe, ±1000 Oe, and ±2000 Oe for the CoFe{sub 2}O{sub 4}, MgFe{sub 2}O{sub 4} and MnFe{sub 2}O{sub 4} respectively, whereas the samples of NiFe{sub 2}O{sub 4} and ZnFe{sub 2}O{sub 4} show a superparamagnetic behavior. Highlights: ► Nanocrystalline MFe{sub 2}O{sub 4} powders were synthesized by a novel hydrothermal method. ► Metal acetylacetonates and aloe vera plant-extracted solution are used. ► This biosynthetic route is very simple and provides high-yield oxide nanomaterials. ► XRD and TEM results indicate that the prepared samples have only spinel structure. ► The maximum M{sub s} of 68.9 emu/g at 10 kOe were observed for the samples of MnFe{sub 2}O{sub 4}. - Abstract: Nanocrystalline spinel ferrite MFe{sub 2}O{sub 4} (M = Ni, Co, Mn, Mg, Zn) powders were synthesized by a novel hydrothermal method using Fe(acac){sub 3}, M(acac){sub 3} (M = Ni, Co, Mn, Mg, Zn) and aloe vera plant extracted solution. The X-ray diffraction and selected-area electron diffraction results indicate that the synthesized nanocrystalline have only spinel structure without the presence of other phase impurities. The crystal structure and morphology of the spinel ferrite powders, as revealed by TEM, show that the NiFe{sub 2}O{sub 4} and CoFe{sub 2}O{sub 4} samples contain nanoparticles, whereas the MnFe{sub 2}O{sub 4} and MgFe{sub 2}O{sub 4} samples consist of many nanoplatelets and nanoparticles. Interestingly, the ZnFe{sub 2}O{sub 4} sample contains plate-like structure of networked nanocrystalline particles. Room temperature magnetization results show a ferromagnetic behavior of the CoFe{sub 2}O{sub 4}, MnFe{sub 2}O{sub 4} and MgFe{sub 2}O{sub 4} samples, whereas the

  2. Structure, morphology and optical properties of undoped and MN-doped ZnO{sub (1−x)}S{sub x} nano-powders prepared by precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Dejene, F.B., E-mail: dejenebf@qwa.ufs.ac.za [Department of Physics, University of the Free State, (Qwa-Qwa campus), Private Bag X-13, Phuthaditjhaba 9866 (South Africa); Onani, M.O. [Chemistry Department, University of the Western Cape, Private Bag x17, Bellville 7535 (South Africa); Koao, L.F.; Wako, A.H.; Motloung, S.V.; Yihunie, M.T. [Department of Physics, University of the Free State, (Qwa-Qwa campus), Private Bag X-13, Phuthaditjhaba 9866 (South Africa)

    2016-01-01

    The undoped and Mn-doped ZnO{sub (1−x)}S{sub x} nano-powders were successfully synthesized by precipitation method without using any capping agent. Its structure, morphology, elemental analysis, optical and luminescence properties were determined by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), UV–vis spectroscopy (UV) and photoluminescence spectroscopy (PL). A typical SEM image of the un-doped ZnO{sub (1−x)}S{sub x} nanoparticles exhibit flake like structures that changes to nearly spherical particles with Mn-doping. The XRD of undoped and Mn doped ZnO{sub (1−x)}S{sub x} pattern reveals the formation of a product indexed to the hexagonal wurtzite phase of ZnS. The nanopowders have crystallite sizes estimated from XRD measurements were in the range of 10–20 nm. All the samples showed absorption maximum of ZnO{sub (1−x)}S{sub x} at 271 nm and high transmittance in UV and visible region, respectively. The undoped ZnO{sub (1−x)}S{sub x} nanoparticles show strong room-temperature photoluminescence with four emission bands centering at 338 nm, 384 nm, 448 nm and 705 nm that may originate to the impurity of ZnO{sub (1−x)}S{sub x}, existence of oxide related defects. The calculated bandgap of the nanocrystalline ZnO{sub (1−x)}S{sub x} showed a blue-shift with respect to the Mn-doping. The PL spectra of the Mn-doped samples exhibit a strong orange emission at around 594 nm attributed to the {sup 4}T{sub 1}–{sup 6}A{sub 1} transition of the Mn{sup 2+} ions.

  3. Magnetic and bioactivity evaluation of ferrimagnetic ZnFe 2O 4 containing glass ceramics for the hyperthermia treatment of cancer

    Science.gov (United States)

    Shah, Saqlain A.; Hashmi, M. U.; Alam, S.; Shamim, A.

    2010-02-01

    Glass ceramics of the composition xZnO·25Fe 2O 3·(40- x)SiO 2·25CaO·7P 2O 5·3Na 2O were prepared by the melt-quench method using oxy-acetylene flame. Glass-powder compacts were sintered at 1100 °C for 3 h and then rapidly cooled at -10 °C. X-ray diffraction (XRD) revealed 3 prominent crystalline phases: ZnFe 2O 4, CaSiO 3 and Ca 10(PO 4) 6(OH) 2. Vibrating sample magnetometer (VSM) data at 10 KOe and 500 Oe showed that saturation magnetization, coercivity and hence hysteresis area increased with the increase in ZnO content. Nano-sized ZnFe 2O 4 crystallites were of pseudo-single domain structure and thus coercivity increased with the increase in crystallite size. ZnFe 2O 4 exhibited ferrimagnetism due to the random distribution of Zn 2+ and Fe 3+ cations at tetrahedral A sites and octahedral B sites. This inversion/random distribution of cations was probably due to the surface effects of nano-ZnFe 2O 4 and rapid cooling of the material from 1100 °C (thus preserving the high temperature state of the random distribution of cations). Calorimetric measurements were carried out using magnetic induction furnace at 500 Oe magnetic field and 400 KHz frequency. The data showed that maximum specific power loss and temperature increase after 2 min were 26 W/g and 37 °C, respectively for the sample containing 10% ZnO. The samples were immersed in simulated body fluid (SBF) for 3 weeks. Scanning electron microscope (SEM), energy dispersive spectroscopy (EDX) and XRD results confirmed the growth of precipitated hydroxyapatite phase after immersion in SBF, suggesting that the ferrimagnetic glass ceramics were bioactive and could bond to the living tissues in physiological environment.

  4. Magnetic and bioactivity evaluation of ferrimagnetic ZnFe2O4 containing glass ceramics for the hyperthermia treatment of cancer

    International Nuclear Information System (INIS)

    Shah, Saqlain A.; Hashmi, M.U.; Alam, S.; Shamim, A.

    2010-01-01

    Glass ceramics of the composition xZnO.25Fe 2 O 3 .(40-x)SiO 2 .25CaO.7P 2 O 5 .3Na 2 O were prepared by the melt-quench method using oxy-acetylene flame. Glass-powder compacts were sintered at 1100 deg. C for 3 h and then rapidly cooled at -10 deg. C. X-ray diffraction (XRD) revealed 3 prominent crystalline phases: ZnFe 2 O 4 , CaSiO 3 and Ca 10 (PO 4 ) 6 (OH) 2 . Vibrating sample magnetometer (VSM) data at 10 KOe and 500 Oe showed that saturation magnetization, coercivity and hence hysteresis area increased with the increase in ZnO content. Nano-sized ZnFe 2 O 4 crystallites were of pseudo-single domain structure and thus coercivity increased with the increase in crystallite size. ZnFe 2 O 4 exhibited ferrimagnetism due to the random distribution of Zn 2+ and Fe 3+ cations at tetrahedral A sites and octahedral B sites. This inversion/random distribution of cations was probably due to the surface effects of nano-ZnFe 2 O 4 and rapid cooling of the material from 1100 deg. C (thus preserving the high temperature state of the random distribution of cations). Calorimetric measurements were carried out using magnetic induction furnace at 500 Oe magnetic field and 400 KHz frequency. The data showed that maximum specific power loss and temperature increase after 2 min were 26 W/g and 37 deg. C, respectively for the sample containing 10% ZnO. The samples were immersed in simulated body fluid (SBF) for 3 weeks. Scanning electron microscope (SEM), energy dispersive spectroscopy (EDX) and XRD results confirmed the growth of precipitated hydroxyapatite phase after immersion in SBF, suggesting that the ferrimagnetic glass ceramics were bioactive and could bond to the living tissues in physiological environment.

  5. In-Flight Formation of Nano-Crystalline Titanium Dioxide Powder in a Plasma Jet and Its Characterization

    International Nuclear Information System (INIS)

    Ananthapadmanabhan, P. V.; Thiyagarajan, T. K.; Sreekumar, K. P.; Vijay, M.; Selvarajan, V.; Yu, Jiaguo; Liu, Shengwei

    2010-01-01

    Nanocrystalline titanium dioxide powder was synthesized by in-flight oxidation of titanium dihydride (TiH 2 ) powder in a thermal plasma jet. TiH 2 powder was injected into the thermal plasma jet and allowed to react with oxygen injected downstream the jet. Characterization of the powder by various analytical tools indicated that the powder consisted of nano-sized titanium dioxide particles consisting predominantly of the anatase phase. It is suggested that the thermo-chemistry of the oxidation process contributes significantly to the formation of nano-sized titania. The large energy released during the oxidation process dissociates the TiO 2 particles into TiO (g) and titanium vapour, which recombine downstream with oxygen and form nano particles of TiO 2 .

  6. Preparation and magnetic properties of nano size nickel ferrite particles using hydrothermal method

    Directory of Open Access Journals (Sweden)

    Nejati Kamellia

    2012-03-01

    Full Text Available Abstract Background Nickel ferrite, a kind of soft magnetic materials is one of the most attracting class of materials due to its interesting and important properties and has many technical applications, such as in catalysis, sensors and so on. In this paper the synthesis of NiFe2O4 nanoparticles by the hydrothermal method is reported and the inhibition of surfactant (Glycerol or Sodium dodecyl sulfate on the particles growth is investigated. Methods For investigation of the inhibition effect of surfactant on NiFe2O4 particles growth, the samples were prepared in presence of Glycerol and Sodium dodecyl sulfate. The X-ray powder diffraction (XRD, transmission electron microscopy (TEM, Fourier transform infrared spectroscopy (FT-IR, vibrating sample magnetometer (VSM and inductively coupled plasma atomic emission spectrometer (ICP-AES techniques were used to characterize the samples. Results The results of XRD and ICP-AES show that the products were pure NiFe2O4 and also nanoparticles grow with increasing the temperature, while surfactant prevents the particle growth under the same condition. The average particle size was determined from the Scherrer's equation and TEM micrographs and found to be in the range of 50-60 nm that decreased up to 10-15 nm in presence of surfactant. The FT-IR results show two absorption bands near to 603 and 490 cm-1 for the tetrahedral and octahedral sites respectively. Furthermore, the saturated magnetization and coercivity of NiFe2O4 nanoparticles were in the range of 39.60 emu/g and 15.67 Qe that decreased for samples prepared in presence of surfactant. As well as, the nanoparticles exhibited a superparamagnetic behavior at room temperature. Conclusions Nanosized nickel ferrite particles were synthesized with and without surfactant assisted hydrothermal methods. The results show that with increasing of temperature, the crystallinity of nanoparticles is increased. In the presence of surfactants, the crystallinity of

  7. Improvement of the tool life of a micro-end mill using nano-sized SiC/Ni electroplating method.

    Science.gov (United States)

    Park, Shinyoung; Kim, Kwang-Su; Roh, Ji Young; Jang, Gyu-Beom; Ahn, Sung-Hoon; Lee, Caroline Sunyong

    2012-04-01

    High mechanical properties of a tungsten carbide micro-end-mill tool was achieved by extending its tool life by electroplating nano-sized SiC particles (electroplating method on the surface of the micro-end-mill tool was applied using SiC particles and Ni particles. Organic additives (saccharin and ammonium chloride) were added in a Watts bath to improve the nickel matrix density in the electroplating bath and to smooth the surface of the co-electroplating. The morphology of the coated nano-sized SiC particles and the composition were measured using Scanning Electron Microscope and Energy Dispersive Spectrometer. As the Ni/SiC co-electroplating layer was applied, the hardness and friction coefficient improved by 50%. Nano-sized SiC particles with 7 wt% were deposited on the surface of the micro-end mill while the Ni matrix was smoothed by adding organic additives. The tool life of the Ni/SiC co-electroplating coating on the micro-end mill was at least 25% longer than that of the existing micro-end mills without Ni/SiC co-electroplating. Thus, nano-sized SiC/Ni coating by electroplating significantly improves the mechanical properties of tungsten carbide micro-end mills.

  8. Effect of Heat Treatment on the Microstructure and Wear Properties of Al-Zn-Mg-Cu/In-Situ Al-9Si-SiCp/Pure Al Composite by Powder Metallurgy

    Science.gov (United States)

    Yu, Byung Chul; Bae, Ki-Chang; Jung, Je Ki; Kim, Yong-Hwan; Park, Yong Ho

    2018-03-01

    This study examined the effects of heat treatment on the microstructure and wear properties of Al-Zn-Mg-Cu/in-situ Al-9Si-SiCp/pure Al composites. Pure Al powder was used to increase densification but it resulted in heterogeneous precipitation as well as differences in hardness among the grains. Heat treatment was conducted to solve this problem. The heat treatment process consisted of three stages: solution treatment, quenching, and aging treatment. After the solution treatment, the main dissolved phases were η'(Mg4Zn7), η(MgZn2), and Al2Cu phase. An aging treatment was conducted over the temperature range, 100-240 °C, for various times. The GP zone and η'(Mg4Zn7) phase precipitated at a low aging temperature of 100-160 °C, whereas the η(MgZn2) phase precipitated at a high aging temperature of 200-240 °C. The hardness of the sample aged at 100-160 °C was higher than that aged at 200-240 °C. The wear test was conducted under various linear speeds with a load of 100 N. The aged composite showed a lower wear rate than that of the as-sintered composite under all conditions. As the linear speed was increased to 1.0 m/s, the predominant wear behavior changed from abrasive to adhesive wear in all composites.

  9. Effect of Heat Treatment on the Microstructure and Wear Properties of Al-Zn-Mg-Cu/In-Situ Al-9Si-SiCp/Pure Al Composite by Powder Metallurgy

    Science.gov (United States)

    Yu, Byung Chul; Bae, Ki-Chang; Jung, Je Ki; Kim, Yong-Hwan; Park, Yong Ho

    2018-05-01

    This study examined the effects of heat treatment on the microstructure and wear properties of Al-Zn-Mg-Cu/in-situ Al-9Si-SiCp/pure Al composites. Pure Al powder was used to increase densification but it resulted in heterogeneous precipitation as well as differences in hardness among the grains. Heat treatment was conducted to solve this problem. The heat treatment process consisted of three stages: solution treatment, quenching, and aging treatment. After the solution treatment, the main dissolved phases were η'(Mg4Zn7), η(MgZn2), and Al2Cu phase. An aging treatment was conducted over the temperature range, 100-240 °C, for various times. The GP zone and η'(Mg4Zn7) phase precipitated at a low aging temperature of 100-160 °C, whereas the η(MgZn2) phase precipitated at a high aging temperature of 200-240 °C. The hardness of the sample aged at 100-160 °C was higher than that aged at 200-240 °C. The wear test was conducted under various linear speeds with a load of 100 N. The aged composite showed a lower wear rate than that of the as-sintered composite under all conditions. As the linear speed was increased to 1.0 m/s, the predominant wear behavior changed from abrasive to adhesive wear in all composites.

  10. Effect of sunlight irradiation on photocatalytic pyrene degradation in contaminated soils by micro-nano size TiO2

    International Nuclear Information System (INIS)

    Chang Chien, S.W.; Chang, C.H.; Chen, S.H.; Wang, M.C.; Madhava Rao, M.; Satya Veni, S.

    2011-01-01

    The enhanced catalytic pyrene degradation in quartz sand and alluvial and red soils by micro-nano size TiO 2 in the presence and absence of sunlight was investigated. The results showed that the synergistic effect of sunlight irradiation and TiO 2 was more efficient on pyrene degradation in quartz sand and red and alluvial soils than the corresponding reaction system without sunlight irradiation. In the presence of sunlight irradiation, the photooxidation (without TiO 2 ) of pyrene was very pronounced in alluvial and red soils and especially in quartz sand. However, in the absence of sunlight irradiation, the catalytic pyrene degradation by TiO 2 and the photooxidation (without TiO 2 ) of pyrene were almost nil. This implicates that ultra-violet (UV) wavelength range of sunlight plays an important role in TiO 2 -enhanced photocatalytic pyrene degradation and in photooxidation (without TiO 2 ) of pyrene. The percentages of photocatalytic pyrene degradation by TiO 2 in quartz sand, alluvial and red soils under sunlight irradiation were 78.3, 23.4, and 31.8%, respectively, at 5 h reaction period with a 5% (w/w) dose of the amended catalyst. The sequence of TiO 2 -enhanced catalytic pyrene degradation in quartz sand and alluvial and red soils was quartz sand > red soil > alluvial soil, due to different texture and total organic carbon (TOC) contents of the quartz sand and other two soils. The differential Fourier transform infrared (FT-IR) spectra of degraded pyrene in alluvial soil corroborate that TiO 2 -enhanced photocatalytic degradation rate of degraded pyrene was much greater than photooxidation (without TiO 2 ) rate of degraded pyrene. Based on the data obtained, the importance for the application of TiO 2 -enhanced photocatalytic pyrene degradation and associated organic contaminants in contaminated soils was elucidated. - Highlights: → Synergistic effect of sunlight irradiation and TiO 2 promoted degradation of pyrene. → Micro-nano size TiO 2 enhanced

  11. Preparation and characterization of nano-sized phase change emulsions as thermal energy storage and transport media

    International Nuclear Information System (INIS)

    Chen, J.; Zhang, P.

    2017-01-01

    Highlights: • The nano-sized phase change emulsions are prepared by using D-phase method. • The thermo-physical and transport properties are experimentally investigated. • The influence of surfactant on the melting temperature and latent heat of water is clarified. • The phase change emulsion can be used as the heat transfer fluid in a thermal energy storage system. - Abstract: Phase change emulsion (PCE) is a kind of two-phase heat transfer fluid with phase change material (PCM) dispersed in carrier fluid. It has received intensive attractions in recent years due to the fact that it can be used as both the thermal energy storage material and transport medium simultaneously in a thermal energy storage system. In the present study, nano-sized PCEs are prepared by the D-phase method with n-hexadecane and n-octadecane as PCMs. The thermo-physical and transport properties are characterized to facilitate the applications. The droplet size distribution of the PCE is measured by a Photon Correlation Spectroscopy, and the results show that the droplet size distributions are similar at different mass fractions. The rheological behavior and viscosity of the PCE are measured by a rheometer, which shows that the PCEs at mass fractions below 30.0 wt% are Newtonian fluids, and the viscosities are dependent on both the mass fraction and temperature. The differential scanning calorimetry (DSC) is employed to analyze the phase change characteristics of the PCE, and the results indicate large supercooling degree of water and PCM in the PCE. The melting temperature and latent heat of water in the PCE are much smaller than those of pure water. The thermal conductivities of the PCE with different mass fractions at different temperatures are measured by the transient hot-wire method. Furthermore, the energy transport characteristics of the PCEs are evaluated on the basis of the measured thermo-physical and transport properties. The results suggest that the PCEs show a drastic

  12. Surface Modification, Characterization and Photocatalytic Performance of Nano-Sized Titania Modified with Silver and Bentonite Clay

    Directory of Open Access Journals (Sweden)

    Neetu Divya

    2009-12-01

    Full Text Available In many textile industries dyes are used as coloring agents. Advanced oxidation processes are used for degrading or removing color from dye baths. Catalysts play a key role in these industries for the treatment of water. Solid catalysts are usually composed of metals that form supports onto the surface and create metal particles with high surface areas. TiO2 composites containing transition metal ions (silver and/or bentonite clay were prepared. Photocatalytic efficiencies have been investigated for the degradation of Orange G an azo dye. Various analytical techniques were used to characterize the surface properties of nano-sized titania modified using silver and/or bentonite clay. Scanning electron microscopy (SEM, Transmission electron microscopy (TEM, X-ray diffraction (XRD and FTIR analyses showed that TiO2 (10 ± 2 nm and Ag (2 to 3 nm particles were supported on the surface of the bentonite clay and the size was in the range of 100 ± 2 nm. The modified catalysts P-25 TiO2/Bentonite/Ag and P-25 TiO2/Ag were found to be very active for the photocatalytic decomposition of Orange G. The percent decolorization in 60 min was 98% with both P-25 TiO2/Ag and P-25 TiO2/Bentonite/Ag modified catalysts. Whereas mineralization achieved in 9 hr were 68% and 71% with P-25 TiO2/Bentonite/Ag and P-25 TiO2/Ag catalyst respectively. © 2009 BCREC UNDIP. All rights reserved[Received: 30 October 2009, Revised: 20 November 2009, Accepted: 21 November 2009][How to Cite: N. Divya, A. Bansal, A. K. Jana. (2009. Surface Modification, Characterization and Photocatalytic Performance of Nano-Sized Titania Modified with Silver and Bentonite Clay. Bulletin of Chemical Reaction Engineering and Catalysis, 4(2: 43-53.  doi:10.9767/bcrec.4.2.1249.43-53][How to Link/ DOI: http://dx.doi.org/10.9767/bcrec.4.2.1249.43-53 || or local: http://ejournal.undip.ac.id/index.php/bcrec/article/view/1249

  13. Nano-sized Li4Ti5O12 anode material with excellent performance prepared by solid state reaction: The effect of precursor size and morphology

    International Nuclear Information System (INIS)

    Li, Xiangru; Hu, Hao; Huang, Sheng; Yu, Gaige; Gao, Lin; Liu, Haowen; Yu, Ying

    2013-01-01

    Graphical abstract: - Highlights: • Nano-sized Li 4 Ti 5 O 12 has been prepared through solid state reaction by using axiolitic TiO 2 as precursor. • The prepared nano-sized Li 4 Ti 5 O 12 anode material shows excellent electrochemical performance. • The utilization of precursor with special morphology and size is one of the useful ways to prepare more active electrode materials. - Abstract: Spinel nano-sized Li 4 Ti 5 O 12 anode material of secondary lithium-ion battery has been successfully prepared by solid state reaction using axiolitic TiO 2 assembled by 10–20 nm nanoparticles and Li 2 CO 3 as precursors. The synthesis condition, grain size effect and corresponding electrochemical performance of the special Li 4 Ti 5 O 12 have been studied in comparison with those of the normal Li 4 Ti 5 O 12 originated from commercial TiO 2 . We also propose the mechanism that using the nano-scaled TiO 2 with special structure and unexcess Li 2 CO 3 as precursors can synthesize pure phase nano-sized Li 4 Ti 5 O 12 at 800 °C through solid state reaction. The prepared nano-sized Li 4 Ti 5 O 12 anode material for Li-ion batteries shows excellent capacity performance with rate capacity of 174.2, 164.0, 157.4, 146.4 and 129.6 mA h g −1 at 0.5, 1, 2, 5 and 10 C, respectively, and capacity retention of 95.1% after 100 cycles at 1 C. In addition, the specific capacity fade for the cell with the different Li 4 Ti 5 O 12 active materials resulted from the increase of internal resistance after 100 cycles is compared

  14. Characterization of coke deposited on nano-sized Pt-Pd/H-beta spent during long-chain paraffin hydroisomerization

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, F.; Einicke, W.D.; Ficht, K.; Glaeser, R. [Leipzig Univ. (Germany). Inst. of Chemical Technology; Bertmer, M. [Leipzig Univ. (Germany). Inst. of Experimental Physics II; Kuchling, T. [Technische Univ. Bergakademie Freiberg (Germany). Inst. of Energy Process Engineering and Chemical Engineering

    2013-11-01

    The hydroisomerization of long-chain n-paraffins were studied in the temperature range 205- 230 C at p{sub H2}=50 bar using a bench scale trickle-bed continuous-flow reactor. The bimetallic catalysts consisted of mixtures of platinum and palladium supported on commercially available nano-sized zeolites Beta (n{sub Si}/n{sub Al} = 12 and 25) extruded with a binder ({gamma}-alumina). For hexadecane conversion, high yields to isomers (25 and 45 wt.% of mono- and multibranched isomers, respectively) without extensive cracking (>10 wt.%) were obtained at a conversion of 80 %. Long-term tests with C{sub 16}H{sub 34} and blends of solid n-paraffins for 30-60 days on stream clearly indicate that a minor loss in catalyst activity can easily be compensated by increasing the reaction temperature from 230 C to 235 C. The zeolite sample with a 'mild acidity' revealed low hydrocracking at isomerization yield up to 70 wt.% and high stability. Carbonaceous deposits formed during n-paraffin hydroisomerization were investigated by temperature-programmed oxidation, elemental analysis, ATR-FTIR and {sup 13}C MAS NMR spectroscopy showing the formation of low-temperature, hydrogen-rich coke. (orig.)

  15. Design and formulation of nano-sized spray dried efavirenz-part I: influence of formulation parameters

    Energy Technology Data Exchange (ETDEWEB)

    Katata, Lebogang, E-mail: lebzakate@yahoo.com; Tshweu, Lesego; Naidoo, Saloshnee; Kalombo, Lonji; Swai, Hulda [Materials Science and Manufacturing, Centre of Polymers and Composites, Council for Scientific and Industrial Research (South Africa)

    2012-11-15

    Efavirenz (EFV) is one of the first-line antiretroviral drugs recommended by the World Health Organisation for treating HIV. It is a hydrophobic drug that suffers from low aqueous solubility (4 {mu}g/mL), which leads to a limited oral absorption and low bioavailability. In order to improve its oral bioavailability, nano-sized polymeric delivery systems are suggested. Spray dried polycaprolactone-efavirenz (PCL-EFV) nanoparticles were prepared by the double emulsion method. The Taguchi method, a statistical design with an L{sub 8} orthogonal array, was implemented to optimise the formulation parameters of PCL-EFV nanoparticles. The types of sugar (lactose or trehalose), surfactant concentration and solvent (dichloromethane and ethyl acetate) were chosen as significant parameters affecting the particle size and polydispersity index (PDI). Small nanoparticles with an average particle size of less than 254 {+-} 0.95 nm in the case of ethyl acetate as organic solvent were obtained as compared to more than 360 {+-} 19.96 nm for dichloromethane. In this study, the type of solvent and sugar were the most influencing parameters of the particle size and PDI. Taguchi method proved to be a quick, valuable tool in optimising the particle size and PDI of PCL-EFV nanoparticles. The optimised experimental values for the nanoparticle size and PDI were 217 {+-} 2.48 nm and 0.093 {+-} 0.02.

  16. Microstructure and Mechanical Properties of Nano-Size Zirconium Carbide Dispersion Strengthened Tungsten Alloys Fabricated by Spark Plasma Sintering Method

    International Nuclear Information System (INIS)

    Xie Zhuoming; Liu Rui; Fang Qianfeng; Zhang Tao; Jiang Yan; Wang Xianping; Liu Changsong

    2015-01-01

    W-(0.2, 0.5, 1.0)wt% ZrC alloys with a relative density above 97.5% were fabricated through the spark plasma sintering (SPS) method. The grain size of W-1.0wt% ZrC is about 2.7 μm, smaller than that of pure W and W-(0.2, 0.5)wt% ZrC. The results indicated that the W-ZrC alloys exhibit higher hardness at room temperature, higher tensile strength at high temperature, and a lower ductile to brittle transition temperature (DBTT) than pure W. The tensile strength and total elongation of W-0.5wt% ZrC alloy at 700 °C is 535 MPa and 24.8%, which are respectively 59% and 114% higher than those of pure W (337 MPa, 11.6%). The DBTT of W-(0.2, 0.5, 1.0)wt% ZrC materials is in the range of 500°C–600°C, which is about 100 °C lower than that of pure W. Based on microstructure analysis, the improved mechanical properties of the W-ZrC alloys were suggested to originate from the enhanced grain boundary cohesion by ZrC capturing the impurity oxygen in tungsten and nano-size ZrC dispersion strengthening. (paper)

  17. Toxicological evaluation of nano-sized colloidal silver in experiments on mice. behavioral reactions, morphology of internals

    Directory of Open Access Journals (Sweden)

    N.V. Zaitseva

    2015-06-01

    Full Text Available The results of toxicity studies of nano-sized colloidal silver (NCC, the most widely used in medicine, food and life, are given. When evaluating safe doses of silver NP (using commercially available NCC solution stabilized with polyvinylpyrrolidone (PVP, with the size of silver NP at the range of 5-80 nm when orally administered to male mice, BALB/c mice at doses of 0.1; 1.0 and 10 mg/kg of body weight per silver different effects from the motor and orienting-exploratory activity were revealed, for the part of them the dependence on the dose of the NCC was typical. The following peculiarities were found: reduction in motor activity to reduce the frequency of activities requiring physical effort, reduction of the execution time of these actions; increasing anxiety in terms of frequency and duration of attacks of orienting-investigative activity and animals washing. Morphological examination revealed a series of tissue changes of internal organs (especially liver and spleen, to a lesser extent – kidney, heart and colon with increase of the spectrum and severity of structural changes with increasing doses of the NCC. From the combination of the data the conclusion was made that maximal ineffective dose (NOAEL of this nanomaterial at subacute oral administration is no more than 0.1 mg/kg body weight.

  18. Magnetic high throughput screening system for the development of nano-sized molecularly imprinted polymers for controlled delivery of curcumin.

    Science.gov (United States)

    Piletska, Elena V; Abd, Bashar H; Krakowiak, Agata S; Parmar, Anitha; Pink, Demi L; Wall, Katie S; Wharton, Luke; Moczko, Ewa; Whitcombe, Michael J; Karim, Kal; Piletsky, Sergey A

    2015-05-07

    Curcumin is a versatile anti-inflammatory and anti-cancer agent known for its low bioavailability, which could be improved by developing materials capable of binding and releasing drug in a controlled fashion. The present study describes the preparation of magnetic nano-sized Molecularly Imprinted Polymers (nanoMIPs) for the controlled delivery of curcumin and their high throughput characterisation using microtitre plates modified with magnetic inserts. NanoMIPs were synthesised using functional monomers chosen with the aid of molecular modelling. The rate of release of curcumin from five polymers was studied under aqueous conditions and was found to correlate well with the binding energies obtained computationally. The presence of specific monomers was shown to be significant in ensuring effective binding of curcumin and to the rate of release obtained. Characterisation of the polymer particles was carried out using dynamic light scattering (DLS) technique and scanning electron microscopy (SEM) in order to establish the relationship between irradiation time and particle size. The protocols optimised during this study could be used as a blueprint for the development of nanoMIPs capable of the controlled release of potentially any compound of interest.

  19. Micro-/Nano- sized hydroxyapatite directs differentiation of rat bone marrow derived mesenchymal stem cells towards an osteoblast lineage

    Science.gov (United States)

    Huang, Yan; Zhou, Gang; Zheng, Lisha; Liu, Haifeng; Niu, Xufeng; Fan, Yubo

    2012-03-01

    Regenerative medicine consisting of cells and materials provides a new way for the repair and regeneration of tissues and organs. Nano-biomaterials are highlighted due to their advantageous features compared with conventional micro-materials. The aim of this study is to investigate the effects of micro-/nano- sized hydroxyapatite (μ/n-HA) on the osteogenic differentiation of rat bone marrow derived mesenchymal stem cells (rBMSCs). μ/n-HA were prepared by a microwave synthesizer and precipitation method, respectively. Different sizes of μ/n-HA were characterized by IR, XRD, SEM, TEM and co-cultured with rBMSCs. It was shown that rBMSCs expressed higher levels of osteoblast-related markers by n-HA than μ-HA stimulation. The size of HA is an important factor for affecting the osteogenic differentiation of rBMSCs. This provides a new avenue for mechanistic studies of stem cell differentiation and a new approach to obtain more committed differentiated cells.

  20. Preparation of Nano-sized Bismuth-Doped Fe3O4 as an Excellent Magnetic Material for Supercapacitor Electrodes

    Science.gov (United States)

    Aghazadeh, Mustafa; Karimzadeh, Isa; Ganjali, Mohammad Reza

    2018-03-01

    Nano-sized Bi3+-doped iron oxide (n-Bi-IO) particles were prepared through a one-pot electrochemical procedure, and the product was evaluated using x-ray diffraction, field-emission scanning electron microscopy and energy-dispersive x-ray spectroscopy. Based on the analyses, the average size of the n-Bi-IO was determined to be 10 nm. Galvanostatic charge-discharge (GCD) evaluations revealed that the specific capacitance of the material reached 235 F g-1 at a discharge condition of 0.2 A g-1. n-Bi-IO had a 94.2% capacity retention after 2000 GCD cycles. Further vibrating sample magnetometery analyses showed that the product has enhanced superparamagnetic qualities (i.e. M r = 0.15 emu g-1 and H Ci = 2.71 G) in comparison to iron oxide nanoparticles (i.e. M r = 0.95 emu g-1 and H Ci = 14.62 G). Given the results, the product is considered to be a promising material for developing high performance supercapacitor electrodes.

  1. Thermal analyses to assess diffusion kinetics in the nano-sized interspaces between the growing crystals of a glass ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Fotheringham, Ulrich, E-mail: ulrich.fotheringham@schott.com [SCHOTT AG, 55014 Mainz (Germany); Wurth, Roman; Ruessel, Christian [Otto-Schott-Institut, Jena University, Jena (Germany)

    2011-08-10

    Highlights: {yields} Macroscopic, routine laboratory methods of the 'Thermal Analysis' type (DSC, DMA) allow a rough description of the kinetics in the nano-sized interstitial spaces of glass ceramics. {yields} These macroscopic measurements support the idea of a rigid zone around the crystals which builds up during ceramization and is part of a negative feedback loop which finally stops crystal growth and Ostwald ripening within the time window of observation. {yields} Ostwald ripening may be provoked by thermally softening said rigid zone. Under certain conditions, this gives rise to a characteristic peak in the DSC. - Abstract: According to a hypothesis by Ruessel and coworkers, the absence of Ostwald ripening during isothermal crystallization of lithium aluminosilicate (LAS) and other glass ceramics indicates the existence of a kinetic hindrance of atomic reorganization in the interstitial spaces between the crystals. Methods of Thermal Analysis (Differential Scanning Calorimetry (DSC), Dynamic Mechanical Analysis (DMA)) which are sensitive to the local atomic rearrangements in the interstitial spaces (including viscous flow) are applied to find support for the idea of kinetic hindrance and the formation of a core shell structure acting as diffusion barrier. Both the DSC-measured calorimetric glass transition and the DMA-measured viscoelastic properties indicate an increase in the time constants of atomic rearrangements and diffusion by at least two orders of magnitude during ceramization. This fits to the above idea. Based on these findings, thermo analytic studies have been performed in order to find out how Ostwald ripening may be provoked.

  2. Effect of microscopic structure on deformation in nano-sized copper and Cu/Si interfacial cracking

    Energy Technology Data Exchange (ETDEWEB)

    Sumigawa, Takashi, E-mail: sumigawa@cyber.kues.kyoto-u.ac.jp; Nakano, Takuya; Kitamura, Takayuki

    2013-03-01

    The purpose of this work is to examine the effect of microscopic structure on the mechanical properties of nano-sized components (nano-components). We developed a bending specimen with a substructure that can be observed by means of a transmission electron microscope (TEM). We examined the plastic behavior of a Cu bi-crystal and the Cu/Si interfacial cracking in a nano-component. TEM images indicated that an initial plastic deformation takes place near the interface edge (the junction between the Cu/Si interface and the surface) in the Cu film with a high critical resolved shear stress (400–420 MPa). The deformation developed preferentially in a single grain. Interfacial cracking took place at the intersection between the grain boundary and the Cu/Si interface, where a high stress concentration existed due to deformation mismatch. These results indicate that the characteristic mechanical behavior of a nano-component is governed by the microscopic stress field, which takes into account the crystallographic structure. - Highlights: ► A nano-component specimen including a bi-crystal copper layer was prepared. ► A loading test with in-situ transmission electron microscopy was conducted. ► The plastic and cracking behaviors were governed by microscopic stress. ► Stress defined under continuum assumption was still present in nano-components.

  3. Design and formulation of nano-sized spray dried efavirenz-part I: influence of formulation parameters

    International Nuclear Information System (INIS)

    Katata, Lebogang; Tshweu, Lesego; Naidoo, Saloshnee; Kalombo, Lonji; Swai, Hulda

    2012-01-01

    Efavirenz (EFV) is one of the first-line antiretroviral drugs recommended by the World Health Organisation for treating HIV. It is a hydrophobic drug that suffers from low aqueous solubility (4 μg/mL), which leads to a limited oral absorption and low bioavailability. In order to improve its oral bioavailability, nano-sized polymeric delivery systems are suggested. Spray dried polycaprolactone-efavirenz (PCL-EFV) nanoparticles were prepared by the double emulsion method. The Taguchi method, a statistical design with an L 8 orthogonal array, was implemented to optimise the formulation parameters of PCL-EFV nanoparticles. The types of sugar (lactose or trehalose), surfactant concentration and solvent (dichloromethane and ethyl acetate) were chosen as significant parameters affecting the particle size and polydispersity index (PDI). Small nanoparticles with an average particle size of less than 254 ± 0.95 nm in the case of ethyl acetate as organic solvent were obtained as compared to more than 360 ± 19.96 nm for dichloromethane. In this study, the type of solvent and sugar were the most influencing parameters of the particle size and PDI. Taguchi method proved to be a quick, valuable tool in optimising the particle size and PDI of PCL-EFV nanoparticles. The optimised experimental values for the nanoparticle size and PDI were 217 ± 2.48 nm and 0.093 ± 0.02.

  4. Controllable synthesis in a continuous mode of unsupported molybdenum catalysts with micro/nano size for heavy oil upgrading

    Energy Technology Data Exchange (ETDEWEB)

    Wang, J.; Hill, J.M.; Pereira Almao, P.R. [Calgary Univ., AB (Canada)

    2004-07-01

    Heavy oils contain significant amounts of impurities compared to conventional oils, thereby posing a challenge for hydroprocessing operations at refineries. Hydrodesulfurization is one of the important reactions involved in hydroprocessing. Transition metal sulfides have excellent properties in terms of sulphur removal. Molybdenum based catalysts have been used extensively in the petroleum industry for hydrotreating heavy oil fractions. Supported molybdenum based catalysts suffer strong deactivation in the traditional hydrotreating process due to the deposition of carbonaceous components on the surface of the catalyst when they are used in conventional fixed bed reactors. Unsupported catalysts have higher catalytic activity with better metal dispersion. Laboratory experiments were conducted in which micro/nano size unsupported molybdenum catalysts were synthesized from a water/oil emulsion. The catalysts were prepared in a continuous mode for online application to hydroprocessing or in situ upgrading. Dispersed molybdenum catalysts are more suitable for processing heavier feeds because they are less prone to deactivation. Also, their submicron size ensure high activities due to a large specific surface area. They are also sufficiently small to be readily dispersed in the residual oil. 4 refs., 1 tab., 2 figs.

  5. MSINDO quantum chemical modeling study of water molecule adsorption at nano-sized anatase TiO2 surfaces

    International Nuclear Information System (INIS)

    Wahab, Hilal S.; Bredow, Thomas; Aliwi, Salah M.

    2008-01-01

    In this work, we studied the adsorption of water molecule onto the (1 0 0), (0 1 0) and (0 0 1) surfaces of nano-sized anatase TiO 2 with semiempirical SCF MO method, MSINDO. The anatase TiO 2 particles are modeled with free clusters (TiO 2 ) n, where n = 20-80. Whereas, the surfaces have been modeled with two saturated clusters, Ti 21 O 58 H 32 and Ti 36 O 90 H 36 . The surface lattice fivefold coordinated titanium atoms (Ti 5C ), which represent the Lewis acid sites, are selected as adsorption centers. We also investigated the effect of TiO 2 cluster size on the computed band gap energy. Results reveal that the electronic properties of a cluster in the lowest excited state differ from that of the ground state. Furthermore, the MSINDO band gap energies of 3.68-3.77 eV for the anatase TiO 2 are in a fair accordance with other literature data. In agreement with other computational and experimental studies, the dissociated form of water molecule adsorption on anatase TiO 2 surfaces is always more stabilized than the molecular form

  6. Huge Inverse Magnetization Generated by Faraday Induction in Nano-Sized Au@Ni Core@Shell Nanoparticles.

    Science.gov (United States)

    Kuo, Chen-Chen; Li, Chi-Yen; Lee, Chi-Hung; Li, Hsiao-Chi; Li, Wen-Hsien

    2015-08-25

    We report on the design and observation of huge inverse magnetizations pointing in the direction opposite to the applied magnetic field, induced in nano-sized amorphous Ni shells deposited on crystalline Au nanoparticles by turning the applied magnetic field off. The magnitude of the induced inverse magnetization is very sensitive to the field reduction rate as well as to the thermal and field processes before turning the magnetic field off, and can be as high as 54% of the magnetization prior to cutting off the applied magnetic field. Memory effect of the induced inverse magnetization is clearly revealed in the relaxation measurements. The relaxation of the inverse magnetization can be described by an exponential decay profile, with a critical exponent that can be effectively tuned by the wait time right after reaching the designated temperature and before the applied magnetic field is turned off. The key to these effects is to have the induced eddy current running beneath the amorphous Ni shells through Faraday induction.

  7. Huge Inverse Magnetization Generated by Faraday Induction in Nano-Sized Au@Ni Core@Shell Nanoparticles

    Directory of Open Access Journals (Sweden)

    Chen-Chen Kuo

    2015-08-01

    Full Text Available We report on the design and observation of huge inverse magnetizations pointing in the direction opposite to the applied magnetic field, induced in nano-sized amorphous Ni shells deposited on crystalline Au nanoparticles by turning the applied magnetic field off. The magnitude of the induced inverse magnetization is very sensitive to the field reduction rate as well as to the thermal and field processes before turning the magnetic field off, and can be as high as 54% of the magnetization prior to cutting off the applied magnetic field. Memory effect of the induced inverse magnetization is clearly revealed in the relaxation measurements. The relaxation of the inverse magnetization can be described by an exponential decay profile, with a critical exponent that can be effectively tuned by the wait time right after reaching the designated temperature and before the applied magnetic field is turned off. The key to these effects is to have the induced eddy current running beneath the amorphous Ni shells through Faraday induction.

  8. Huge Inverse Magnetization Generated by Faraday Induction in Nano-Sized Au@Ni Core@Shell Nanoparticles

    Science.gov (United States)

    Kuo, Chen-Chen; Li, Chi-Yen; Lee, Chi-Hung; Li, Hsiao-Chi; Li, Wen-Hsien

    2015-01-01

    We report on the design and observation of huge inverse magnetizations pointing in the direction opposite to the applied magnetic field, induced in nano-sized amorphous Ni shells deposited on crystalline Au nanoparticles by turning the applied magnetic field off. The magnitude of the induced inverse magnetization is very sensitive to the field reduction rate as well as to the thermal and field processes before turning the magnetic field off, and can be as high as 54% of the magnetization prior to cutting off the applied magnetic field. Memory effect of the induced inverse magnetization is clearly revealed in the relaxation measurements. The relaxation of the inverse magnetization can be described by an exponential decay profile, with a critical exponent that can be effectively tuned by the wait time right after reaching the designated temperature and before the applied magnetic field is turned off. The key to these effects is to have the induced eddy current running beneath the amorphous Ni shells through Faraday induction. PMID:26307983

  9. Effect of Co2+ and Y3+ ions insertion on the microstructure development and magnetic properties of Ni0.5Zn0.5Fe2O4 powders synthesized using Co-precipitation method

    Science.gov (United States)

    Rashad, M. M.; Rayan, D. A.; Turky, A. O.; Hessien, M. M.

    2015-01-01

    Nanocrystalline Ni0.5Zn0.5-xCoxFe2-zYzO4 powders (x=0-0.3 and z from 0 to 0.3) have been synthesized via a facile co-precipitation technique. X-ray diffraction (XRD), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM) are utilized in order to study the effect of variation of cobalt and yttrium substitutions and its impact on crystalline size, lattice parameter, X-ray density, microstructure and magnetic properties of the formed powders. X-ray diffraction data indicated that, after doping, all samples consisted of the main spinel phase for the formed precursors precipitated at pH 10 annealed at 1000 oC for 2 h. The lattice parameter and the unit cell were decreased linearly with increasing Co content whereas they were increased with increasing the Y incorporation. Additionally, the porosity was increased with increasing Co concentration while it was decreased with increasing the Y insertion. The mean ionic radii and hopping and bond lengths was decreased with the value of Co2+ and they were increased with the value of Y3+ ion as well as both of Y3+ and Co2+ ions. The microstructures of the produced powders were found to be cubic like structure. The addition of Y3+ ion suppressed the grain size whereas addition of Co2+ ion enhanced the grain growth availably. An examination of the magnetic properties revealed an increase in saturation magnetization with increasing Co and Y concentrations incorporation up to x=0.3. Meanwhile, the formed powders exhibited superparamagnetic characteristics. A high saturation magnetization (77.0 emu/g) was achieved for Ni0.5Zn0.2Co0.3Fe2O4 sample annealed at 1000 oC for 2 h.

  10. Nano-Sized Structurally Disordered Metal Oxide Composite Aerogels as High-Power Anodes in Hybrid Supercapacitors.

    Science.gov (United States)

    Huang, Haijian; Wang, Xing; Tervoort, Elena; Zeng, Guobo; Liu, Tian; Chen, Xi; Sologubenko, Alla; Niederberger, Markus

    2018-03-27

    A general method for preparing nano-sized metal oxide nanoparticles with highly disordered crystal structure and their processing into stable aqueous dispersions is presented. With these nanoparticles as building blocks, a series of nanoparticles@reduced graphene oxide (rGO) composite aerogels are fabricated and directly used as high-power anodes for lithium-ion hybrid supercapacitors (Li-HSCs). To clarify the effect of the degree of disorder, control samples of crystalline nanoparticles with similar particle size are prepared. The results indicate that the structurally disordered samples show a significantly enhanced electrochemical performance compared to the crystalline counterparts. In particular, structurally disordered Ni x Fe y O z @rGO delivers a capacity of 388 mAh g -1 at 5 A g -1 , which is 6 times that of the crystalline sample. Disordered Ni x Fe y O z @rGO is taken as an example to study the reasons for the enhanced performance. Compared with the crystalline sample, density functional theory calculations reveal a smaller volume expansion during Li + insertion for the structurally disordered Ni x Fe y O z nanoparticles, and they are found to exhibit larger pseudocapacitive effects. Combined with an activated carbon (AC) cathode, full-cell tests of the lithium-ion hybrid supercapacitors are performed, demonstrating that the structurally disordered metal oxide nanoparticles@rGO||AC hybrid systems deliver high energy and power densities within the voltage range of 1.0-4.0 V. These results indicate that structurally disordered nanomaterials might be interesting candidates for exploring high-power anodes for Li-HSCs.

  11. Bactericidal Effect of Lauric Acid-Loaded PCL-PEG-PCL Nano-Sized Micelles on Skin Commensal Propionibacterium acnes

    Directory of Open Access Journals (Sweden)

    Thi-Quynh-Mai Tran

    2016-08-01

    Full Text Available Acne is the over growth of the commensal bacteria Propionibacterium acnes (P. acnes on human skin. Lauric acid (LA has been investigated as an effective candidate to suppress the activity of P. acnes. Although LA is nearly insoluble in water, dimethyl sulfoxide (DMSO has been reported to effectively solubilize LA. However, the toxicity of DMSO can limit the use of LA on the skin. In this study, LA-loaded poly(ɛ-caprolactone-poly(ethylene glycol-poly(ɛ-caprolactone micelles (PCL-PEG-PCL were developed to improve the bactericidal effect of free LA on P. acnes. The block copolymers mPEG-PCL and PCL-PEG-PCL with different molecular weights were synthesized and characterized using 1H Nuclear Magnetic Resonance spectroscopy (1H NMR, Fourier-transform infrared spectroscopy (FT-IR, Gel Permeation Chromatography (GPC, and Differential Scanning Calorimetry (DSC. In the presence of LA, mPEG-PCL diblock copolymers did not self-assemble into nano-sized micelles. On the contrary, the average particle sizes of the PCL-PEG-PCL micelles ranged from 50–198 nm for blank micelles and 27–89 nm for LA-loaded micelles. The drug loading content increased as the molecular weight of PCL-PEG-PCL polymer increased. Additionally, the minimum inhibitory concentration (MIC and the minimum bactericidal concentration (MBC of free LA were 20 and 80 μg/mL, respectively. The MICs and MBCs of the micelles decreased to 10 and 40 μg/mL, respectively. This study demonstrated that the LA-loaded micelles are a potential treatment for acne.

  12. Effect of a nano-sized TiC particle addition on the flow-assisted corrosion resistance of SA 106B carbon steel

    Science.gov (United States)

    Park, Jin-Ju; Park, Eun-Kwang; Lee, Gyoung-Ja; Rhee, Chang-Kyu; Lee, Min-Ku

    2017-09-01

    Carbon steel with dispersed nano-sized TiC ceramic particles was fabricated by the ex-situ introduction of the particles into the melt, with the flow-assisted corrosion (FAC) resistance then investigated in the presence and absence of TiC nanoparticles using a once-through type of FAC loop test. From the potentiodynamic polarization curves, the current density at any given anodic potential was decreased and the open-circuit potential was increased by the addition of TiC nanoparticles. In addition, when the nano-sized TiC particles were added, the FAC rate was 1.38 times lower than that of carbon steel without TiC nanoparticles, indicating an improvement of the FAC resistance due to the homogeneous distribution of the TiC reinforcing nanoparticles.

  13. Nano-sized LiFePO4/C composite with core-shell structure as cathode material for lithium ion battery

    International Nuclear Information System (INIS)

    Liu, Yang; Zhang, Min; Li, Ying; Hu, Yemin; Zhu, Mingyuan; Jin, Hongming; Li, Wenxian

    2015-01-01

    Graphical abstract: Nano-sized LiFePO4/C composite with core-shell structure was fabricated via a well-designed approach as cathode material forlithium ion battery. The nano-sized LiFePO4/C composite with whole carbon shell coating layer showed an excellent electrical performance. - Abstract: Nano-sized composite with LiFePO 4 -core and carbon-shell was synthesized via a facile route followed by heat treatment at 650 °C. X-ray diffraction (XRD) shows that the core is well crystallized LiFePO 4 . The electron microscopy (SEM and TEM) observations show that the core-shell structured LiFePO 4 /C composite coating with whole carbon shell layer of ∼2.8 nm, possesses a specific surface area of 51 m 2 g −1 . As cathode material for lithium ion battery, the core-shell LiFePO 4 /C composite exhibits high initial capacity of 161 mAh g −1 at 0.1 C, excellent high-rate discharge capacity of 135 mAh g −1 at 5 C and perfect cycling retention of 99.6% at 100 th cycle. All these promising results should be contributed to the core-shell nanostructure which prevents collapse of the particle structure in the long-term charge and discharge cycles, as well as the large surface area of the nano-sized LiFePO 4 /C composite which enhances the electronic conductivity and shortens the distance of lithium ion diffusion

  14. Synthesis from zinc oxalate, growth mechanism and optical properties of ZnO nano/micro structures

    Energy Technology Data Exchange (ETDEWEB)

    Raj, C. Justin; Varma, K.B.R. [Materials Research Centre, Indian Institute of Science, Bangalore 560 012 (India); Joshi, R.K. [Special Center for Nano Sciences, Jawaharlal Nehru University, New Delhi 110067 (India)

    2011-11-15

    We report the synthesis of various morphological micro to nano structured zinc oxide crystals via simple precipitation technique. The growth mechanisms of the zinc oxide nanostructures such as snowflake, rose, platelets, porous pyramid and rectangular shapes were studied in detail under various growth conditions. The precursor powders were prepared using several zinc counter ions such as chloride, nitrate and sulphate along with oxalic acid as a precipitating agent. The precursors were decomposed by heating in air resulting in the formation of different shapes of zinc oxide crystals. Variations in ZnO nanostructural shapes were possibly due to the counter ion effect. Sulphate counter ion led to unusual rose-shape morphology. Strong ultrasonic treatment on ZnO rose shows that it was formed by irregular arrangement of micro to nano size hexagonal zinc oxide platelets. The X-ray diffraction studies confirmed the wurzite structure of all zinc oxide samples synthesized using different zinc counter ions. Functional groups of the zinc oxalate precursor and zinc oxide were identified using micro Raman studies. The blue light emission spectra of the various morphologies were recorded using luminescence spectrometer. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  15. Effects of ultrasonic vibration on microstructure and mechanical properties of nano-sized SiC particles reinforced Al-5Cu composites.

    Science.gov (United States)

    Li, Jianyu; Lü, Shulin; Wu, Shusen; Gao, Qi

    2018-04-01

    Ultrasonic vibration (UV) treatment has been successfully applied to improve the particles distribution of nano-sized SiC particles (SiC p ) reinforced Al-5Cu alloy matrix composites which were prepared by combined processes of dry high energy ball milling and squeeze casting. When UV treatment is applied, the distribution of nano-sized SiC p has been greatly improved. After UV for 1 min, large particles aggregates are broken up into small aggregates due to effects of cavitation and the acoustic streaming. After UV for 5 min, all the particles aggregates are dispersed and the particles are uniformly distributed in the composites. Compared with the Al-5Cu matrix alloy, the ultimate tensile strength, yield strength and elongation of the 1 wt% nano-sized SiC p /Al-5Cu composites treated by UV for 5 min are 270 MPa, 173 MPa and 13.3%, which are increased by 7.6%, 6.8% and 29%, respectively. The improvements of mechanical properties after UV are attributed to the uniform distribution of nano particles, grain refinement of aluminum matrix alloy and reduction of porosity in the composites. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Exposure to nano-size titanium dioxide causes oxidative damages in human mesothelial cells: The crystal form rather than size of particle contributes to cytotoxicity.

    Science.gov (United States)

    Hattori, Kenji; Nakadate, Kazuhiko; Morii, Akane; Noguchi, Takumi; Ogasawara, Yuki; Ishii, Kazuyuki

    2017-10-14

    Exposure to nanoparticles such as carbon nanotubes has been shown to cause pleural mesothelioma similar to that caused by asbestos, and has become an environmental health issue. Not only is the percutaneous absorption of nano-size titanium dioxide particles frequently considered problematic, but the possibility of absorption into the body through the pulmonary route is also a concern. Nevertheless, there are few reports of nano-size titanium dioxide particles on respiratory organ exposure and dynamics or on the mechanism of toxicity. In this study, we focused on the morphology as well as the size of titanium dioxide particles. In comparing the effects between nano-size anatase and rutile titanium dioxide on human-derived pleural mesothelial cells, the anatase form was shown to be actively absorbed into cells, producing reactive oxygen species and causing oxidative damage to DNA. In contrast, we showed for the first time that the rutile form is not easily absorbed by cells and, therefore, does not cause oxidative DNA damage and is significantly less damaging to cells. These results suggest that with respect to the toxicity of titanium dioxide particles on human-derived mesothelial cells, the crystal form rather than the particle size has a greater effect on cellular absorption. Also, it was indicated that the difference in absorption is the primary cause of the difference in the toxicity against mesothelial cells. Copyright © 2017 Elsevier Inc. All rights reserved.

  17. Formation of modified TbCu{sub 7} and Th{sub 2}Zn{sub 17} type structures during annealing of mechanical-alloyed Sm-Fe powders

    Energy Technology Data Exchange (ETDEWEB)

    Teresiak, A.; Kubis, M.; Mattern, N.; Wolf, M.; Mueller, K.-H. [Inst. fuer Festkoerper- und Werkstofforschung, Dresden (Germany)

    1998-06-26

    Compounds with the nominal composition near Sm{sub 2}Fe{sub 17} were prepared by mechanical alloying starting from the elemental powders and subsequent annealing at temperatures, T{sub A}, between 600 C and 900 C. For crystal structure investigations of the non-equilibrium phases formed at various temperatures, XRD methods with following Rietveld analysis were applied. For T{sub A} between 600 C and 750 C a modified TbCu{sub 7}-type structure of space group P6/mmm was found, in which the Fe(2c) site is replaced by the partially (1/3) and randomly occupied Fe(6l) site. Its approximate composition is SmFe{sub 8.8-9.0}. For T{sub A} between 800 C to 900 C a disordered modified Th{sub 2}Zn{sub 17} structure (space group R anti 3m) was found that is formed by introducing additional randomly occupied Fe (6c) and Sm(3a) positions, respectively. The degree of order of Sm atoms and Fe-dumbbells along the c-direction increases with increasing T{sub A}. A decrease in the Fe concentration in the cell is observed for increasing T{sub A}. The completely ordered stoichiometric Th{sub 2}Zn{sub 17}-type structure could not be reached by annealing samples prepared from the ball-milled elemental powders. (orig.) 20 refs.

  18. Observation of nano sized effect on EPR of Mn.sup.4+./sup. and Cr.sup.3+./sup. in SrTiO.sub.3./sub. powders

    Czech Academy of Sciences Publication Activity Database

    Badalyan, A. G.; Azamat, Dmitry; Trepakov, Vladimír; Makarova, Marina; Rosa, Jan; Dejneka, Alexandr; Jastrabík, Lubomír

    2015-01-01

    Roč. 485, č. 1 (2015), s. 63-67 ISSN 0015-0193 R&D Projects: GA MŠk LO1409; GA TA ČR TA03010743 Institutional support: RVO:68378271 Keywords : EPR * nanopowder * strontium titanate Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.491, year: 2015

  19. Toxicological aspects of photocatalytic degradation of selected xenobiotics with nano-sized Mn-doped TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Ozmen, Murat, E-mail: murat.ozmen@inonu.edu.tr [Inonu University, Faculty of Science, Department of Biology, Malatya (Turkey); Güngördü, Abbas [Inonu University, Faculty of Science, Department of Biology, Malatya (Turkey); Erdemoglu, Sema [Inonu University, Faculty of Science, Department of Chemistry, Malatya (Turkey); Ozmen, Nesrin [Inonu University, Faculty of Education, Department of Science Teaching Program, Malatya (Turkey); Asilturk, Meltem [Akdeniz University, Department of Materials Science and Engineering, Antalya (Turkey)

    2015-08-15

    Highlights: • Undoped and Mn-doped TiO{sub 2} nanoparticles were synthesized and characterized. • The photocatalytic efficiency of the photocatalysts was evaluated for BPA and ATZ. • Toxicity of photocatalysts and photocatalytic by-products were determined. • Mn-doped TiO{sub 2} nanoparticles did not cause significant lethality on X. laevis. • Degradation of BPA caused a significant reduction of lethal effects. - Abstract: The toxic effects of two selected xenobiotics, bisphenol A (BPA) and atrazine (ATZ), were evaluated after photocatalytic degradation using nano-sized, Mn-doped TiO{sub 2}. Undoped and Mn-doped TiO{sub 2} nanoparticles were synthesized. The samples were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), UV–vis-diffuse reflectance spectra (DRS), X-ray fluorescence spectroscopy (XRF), and BET surface area. The photocatalytic efficiency of the undoped and Mn-doped TiO{sub 2} was evaluated for BPA and ATZ. The toxicity of the synthesized photocatalysts and photocatalytic by-products of BPA and ATZ was determined using frog embryos and tadpoles, zebrafish embryos, and bioluminescent bacteria. Possible toxic effects were also evaluated using selected enzyme biomarkers. The results showed that Mn-doped TiO{sub 2} nanoparticles did not cause significant lethality in Xenopus laevis embryos and tadpoles, but nonfiltered samples caused lethality in zebrafish. Furthermore, Mn-doping of TiO{sub 2} increased the photocatalytic degradation capability of nanoparticles, and it successfully degraded BPA and AZT, but degradation of AZT caused an increase of the lethal effects on both tadpoles and fish embryos. Degradation of BPA caused a significant reduction of lethal effects, especially after 2–4 h of degradation. However, biochemical assays showed that both Mn-doped TiO{sub 2} and the degradation by-products caused a significant change of selected biomarkers on X. laevis tadpoles; thus, the ecological risks of Mn

  20. The influence of size on the toxicity of an encapsulated pesticide: a comparison of micron- and nano-sized capsules.

    Science.gov (United States)

    Meredith, Alicea N; Harper, Bryan; Harper, Stacey L

    2016-01-01

    Encapsulation technology involves entrapping a chemical active ingredient (a.i.) inside a hollow polymeric shell and has been applied to commercial pesticide manufacturing for years to produce capsule suspension (CS) formulations with average particle sizes in the micron-scale. The few literature sources that investigate the environmental fate and toxicity to non-target organisms of encapsulated commercially available pesticide products with regard to capsule size report on average sizes between 20 and 50 μm. Here, we have identified a CS formulation with an average capsule size of approximately 2 μm with some capsules extending into the nanometer scale (~200 nm). Determining how carrier size influences toxicity is important to understanding if current pesticide risk assessments are sufficient to protect against products that incorporate encapsulation technology. Here, a commercial pyrethroid CS pesticide with lambda-cyhalothrin (λ-Cy) as the a.i. was separated into two suspensions, a fraction consisting of nano-sized capsules (~250 nm) and a fraction of micron-sized capsules (~2200 nm) in order to investigate the influence of capsule size on toxicity to embryonic zebrafish, Danio rerio. Toxicity was evaluated 24h after exposure to equivalent amounts of a.i. by the presence and severity of pyrethroid-specific tremors, 14 sublethal developmental impacts and mortality. Fish exposed to greater than 20 μg a.i. L(-1) technical λ-Cy or formulated product experienced curvature of the body axis, pericardial edema, craniofacial malformations, and mortality. Exposure to the unfractionated formulation, micro fraction, nano fraction and technical a.i. resulted in no significant differences in the occurrence of sublethal impacts or mortality; however, the technical a.i. exposure resulted in significantly less fish experiencing tremors and shorter tremors compared to any of the formulated product exposures. This suggests that the capsule size does not influence the toxic

  1. Chemical and electrochemical synthesis of nano-sized TiO{sub 2} anatase for large-area photon conversion

    Energy Technology Data Exchange (ETDEWEB)

    Babasaheb, Raghunath Sankapal; Shrikrishna, Dattatraya Sartale; Lux-Steiner, M.Ch.; Ennaoui, A. [Hahn-Meitner-Institut, Div. of Solar Energy Research, Berlin (Germany)

    2006-05-15

    We report on the synthesis of nanocrystalline titanium dioxide thin films and powders by chemical and electrochemical deposition methods. Both methods are simple, inexpensive and suitable for large-scale production. Air-annealing of the films and powders at T = 500 C leads to densely packed nanometer sized anatase TiO{sub 2} particles. The obtained layers are characterized by different methods such as: X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Titanium dioxide TiO{sub 2} (anatase) phase with (101) preferred orientation has been obtained for the films deposited on glass; indium doped tin oxide (ITO) and quartz substrates. The powder obtained as the byproduct consists of TiO{sub 2} with anatase-phase as well. (authors)

  2. Chemical and electrochemical synthesis of nano-sized TiO2 anatase for large-area photon conversion

    International Nuclear Information System (INIS)

    Babasaheb, Raghunath Sankapal; Shrikrishna, Dattatraya Sartale; Lux-Steiner, M.Ch.; Ennaoui, A.

    2006-01-01

    We report on the synthesis of nanocrystalline titanium dioxide thin films and powders by chemical and electrochemical deposition methods. Both methods are simple, inexpensive and suitable for large-scale production. Air-annealing of the films and powders at T = 500 C leads to densely packed nanometer sized anatase TiO 2 particles. The obtained layers are characterized by different methods such as: X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Titanium dioxide TiO 2 (anatase) phase with (101) preferred orientation has been obtained for the films deposited on glass; indium doped tin oxide (ITO) and quartz substrates. The powder obtained as the byproduct consists of TiO 2 with anatase-phase as well. (authors)

  3. Synthesis and characterization of ZnO–CuO nanocomposites powder by modified perfume spray pyrolysis method and its antimicrobial investigation

    Science.gov (United States)

    Saravanakkumar, D.; Sivaranjani, S.; Kaviyarasu, K.; Ayeshamariam, A.; Ravikumar, B.; Pandiarajan, S.; Veeralakshmi, C.; Jayachandran, M.; Maaza, M.

    2018-03-01

    Pure ZnO, ZnO–CuO nanocomposites can be synthesized by using a modified perfume spray pyrolysis method (MSP). The crystallite size of the nanoparticles (NPs) has been observed by X-ray diffraction pattern and is nearly 36 nm. Morphological studies have been analyzed by using Field Emission Scanning Electron Microscopy (FESEM) and its elemental analysis was reported by Elemental X-ray Analysis (EDX); these studies confirmed that ZnO and CuO have hexagonal structure and monoclinic structure respectively. Fourier Transform Infrared (FTIR) spectra revealed that the presence of functional frequencies of ZnO and CuO were observed at 443 and 616 cm‑1. The average bandgap value at 3.25 eV using UV–vis spectra for the entitled composite has described a blue shift that has been observed here. The antibacterial study against both gram positive and negative bacteria has been studied by the disc diffusion method. To the best of our knowledge, it is the first report on ZnO–CuO nanocomposite synthesized by a modified perfume spray pyrolysis method.

  4. Characterisation of micro-sized and nano-sized tungsten oxide-epoxy composites for radiation shielding of diagnostic X-rays

    Energy Technology Data Exchange (ETDEWEB)

    Noor Azman, N.Z. [Department of Imaging and Applied Physics, Curtin University, GPO Box U1987, Perth, WA 6845 Australia (Australia); School of Physics, Universiti Sains Malaysia, 11800 Penang (Malaysia); Siddiqui, S.A. [Department of Imaging and Applied Physics, Curtin University, GPO Box U1987, Perth, WA 6845 Australia (Australia); Low, I.M., E-mail: j.low@curtin.edu.au [Department of Imaging and Applied Physics, Curtin University, GPO Box U1987, Perth, WA 6845 Australia (Australia)

    2013-12-01

    Characteristics of X-ray transmissions were investigated for epoxy composites filled with 2–10 vol% WO{sub 3} loadings using synchrotron X-ray absorption spectroscopy (XAS) at 10–40 keV. The results obtained were used to determine the equivalent X-ray energies for the operating X-ray tube voltages of mammography and radiology machines. The results confirmed the superior attenuation ability of nano-sized WO{sub 3}-epoxy composites in the energy range of 10–25 keV when compared to their micro-sized counterparts. However, at higher synchrotron radiation energies (i.e., 30–40 keV), the X-ray transmission characteristics were similar with no apparent size effect for both nano-sized and micro-sized WO{sub 3}-epoxy composites. The equivalent X-ray energies for the operating X-ray tube voltages of the mammography unit (25–49 kV) were in the range of 15–25 keV. Similarly, for a radiology unit operating at 40–60 kV, the equivalent energy range was 25–40 keV, and for operating voltages greater than 60 kV (i.e., 70–100 kV), the equivalent energy was in excess of 40 keV. The mechanical properties of epoxy composites increased initially with an increase in the filler loading but a further increase in the WO{sub 3} loading resulted in deterioration of flexural strength, modulus and hardness. - Highlights: • Nano-sized WO{sub 3}-epoxy composites have superior x-ray shielding capability. • No size effect in x-ray attenuation was observed at 30–40 keV. • An optimum filler loading for improving the mechanical properties of WO{sub 3}-epoxy composites.

  5. Development of nano-sized {alpha}-Al{sub 2}O{sub 3}:C films for application in digital radiology

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Edna C., E-mail: edca@cdtn.b [Universidade Federal de Minas Gerais (DEN/UFMG), Belo Horizonte (Brazil). Dept. de Engenharia Nuclear; Fontainha, Crissia C. [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte (Brazil). Dept. de Propedeutica Complemetar; Oliveira, Vitor H.; Ferraz, Wilmar B.; Faria, Luiz O. [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2011-07-01

    Ceramic materials are widely used as sensors for ionizing radiation. In nuclear applications, the alpha-alumina doped with carbon ({alpha}-Al{sub 2}O{sub 3}:C) is the most widely ceramic used because of its excellent optically stimulated luminescence (OSL) and thermoluminescent (TL) properties applied to detection of ionizing radiation. Another application of OSL and TL materials are in Digital Radiography, with ceramic/polymeric film composites. Recently, Computed Radiography (CR) devices based on OSL materials are replacing the old conventional film radiography. In this study we investigate the thermoluminescence of nano-sized {alpha}-Al{sub 2}O{sub 3} samples doped with different percentages of carbon, sintered in reducing atmospheres at temperatures ranging from 1300 to 1750 deg C. The results indicate that the nano-sized {alpha}-Al{sub 2}O{sub 3}:C materials have a luminescent response that could be due to both OSL and RPL properties, but without application to radiation dosimetry. Moreover, the results indicate that micro-sized {alpha}-Al{sub 2}O{sub 3}:C, doped with 0.5% carbon, and nano-sized ones doped with 2% of carbon, present thermoluminescent signal around 30 to 100 times the TL output signal of commercial TLD-100, the most used TL dosimeter in the world. The results indicate that these ceramic nano-particles have great potential for use in Digital Radiography based on thermoluminescent film imaging, being able to provide image resolutions much higher than the micro-sized {alpha}-Al{sub 2}O{sub 3}:C, in view of their improved resolution provided by nano-particulates. (author)

  6. Effect of deep cryogenic treatment on the formation of nano-sized carbides and the wear behavior of D2 tool steel

    Science.gov (United States)

    Amini, Kamran; Akhbarizadeh, Amin; Javadpour, Sirus

    2012-09-01

    The effect of deep cryogenic treatment on the microstructure, hardness, and wear behavior of D2 tool steel was studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), hardness test, pin-on-disk wear test, and the reciprocating pin-on-flat wear test. The results show that deep cryogenic treatment eliminates retained austenite, makes a better carbide distribution, and increases the carbide content. Furthermore, some new nano-sized carbides form during the deep cryogenic treatment, thereby increasing the hardness and improving the wear behavior of the samples.

  7. 197Au Moessbauer study of nano-sized gold catalysts supported on Mg(OH)2 and TiO2

    International Nuclear Information System (INIS)

    Kobayashi, Y.; Nasu, S.; Tsubota, S.; Haruta, M.

    2000-01-01

    We have studied nano-sized Au catalysts supported on Mg(OH) 2 and TiO 2 using 197 Au Moessbauer spectroscopy. 197 Au Moessbauer spectra observed for Au/Mg(OH) 2 catalysts can be decomposed into one singlet with zero isomer shift and several doublets. One of the doublets shows an isomer shift that is typical for Au I , and other doublets are due to Au III . The relative area of the Au I component shows the maximum value for a specimen calcined at 523 K, which also shows the highest catalytic activity

  8. Microstructural and nonlinear optical properties of Bi.sub.2./sub.ZnB.sub.2./sub.O.sub.7./sub.:RE.sup.3+./sup. powders

    Czech Academy of Sciences Publication Activity Database

    Chrunik, M.; Majchrowski, A.; Szala, M.; Zasada, D.; Kroupa, Jan; Bubnov, Alexej; Chlanda, E.; Wozniak, M.J.

    2017-01-01

    Roč. 694, Feb (2017), s. 959-970 ISSN 0925-8388 R&D Projects: GA MŠk 7AMB13PL041; GA ČR GA15-02843S Grant - others:EU - ICT(XE) COST Action IC1208 Institutional support: RVO:68378271 Keywords : rare earth doped borates * nonlinear materials * powder synthesis * nanoparticles Subject RIV: JJ - Other Materials OBOR OECD: Nano-materials (production and properties) Impact factor: 3.133, year: 2016

  9. A Novel Composite Material Designed from FeSi Powder and Mn0.8Zn0.2Fe2O4 Ferrite

    Czech Academy of Sciences Publication Activity Database

    Strečková, M.; Bureš, R.; Fáberová, M.; Kurek, P.; Roupcová, Pavla; Hadraba, Hynek; Girman, V.; Strečka, J.

    2015-01-01

    Roč. 2015, č. 1 (2015), Art. n. 924859 ISSN 1687-8434 R&D Projects: GA MŠk(CZ) ED1.1.00/02.0068; GA ČR(CZ) GAP108/11/1350 Institutional support: RVO:68081723 Keywords : soft-magnetic composite s * Mn-Zn ferrites * nanoparticles * coprecipitation * combustion * batteries Subject RIV: JG - Metallurgy Impact factor: 1.010, year: 2015

  10. Investigation of structural and magnetic properties of Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} nano powders prepared by self combustion method

    Energy Technology Data Exchange (ETDEWEB)

    Sudheesh, V.D.; Nehra, J.; Vinesh, A. [Department of Physics, Mohanlal Sukhadia University, Udaipur 313001, Rajasthan (India); Sebastian, V. [Department of Physics, Nirmalagiri College, Kuthuparamba 670701, Kerala (India); Lakshmi, N., E-mail: nambakkat@yahoo.com [Department of Physics, Mohanlal Sukhadia University, Udaipur 313001, Rajasthan (India); Dutta, Dimple P. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Reddy, V.R. [UGC-DAE CSR, University Campus, Khandwa Road, Indore 452001, M.P. (India); Venugopalan, K. [Department of Physics, Mohanlal Sukhadia University, Udaipur 313001, Rajasthan (India); Gupta, Ajay [UGC-DAE CSR, University Campus, Khandwa Road, Indore 452001, M.P. (India)

    2013-02-15

    Graphical abstract: Display Omitted Highlights: ► Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} prepared by self combustion with uniform/nonuniform heating. ► Characterized using TEM, XRD, in-field Mössbauer and DC magnetometry. ► Leads to bimodal (S1) and very narrow size distribution (S2) type nano samples. ► S1 has magnetic properties of bulk Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4}. ► Although very even sized, S2 large magnetic anisotropy distribution. -- Abstract: Nano powders of Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} have been synthesized by the self-combustion method at a relatively low temperature of 473 K under conditions of non-uniform and uniform heating. Rietveld fitting of X-ray diffractograms confirm the formation of the pure spinel phase in both samples. Transmission electron microscopy indicates that the sample prepared under non-uniform heating has a bimodal particle size distribution (average values 16 nm and 6 nm) while the one prepared under uniform heating has a very narrow particle size distribution (average size 4 nm). Low temperature, in-field Mössbauer spectroscopic studies clearly show surface spin contributions. The hyperfine fields and Curie temperature of the non-uniformly heated sample are in good agreement with those reported for the corresponding bulk samples. Despite having a very narrow particle size distribution, the uniformly heated sample has a large anisotropy distribution which is evident in the broad transition visible in the temperature dependent magnetization curve. It is also corroborated by the fact that the experimental magnetization curve at room temperature requires two Langevin functions for satisfactory reproduction.

  11. The Effect of Nano sized Carbon Black on the Physical and Thermomechanical Properties of Al2O3-SiC-SiO2-C Composite

    International Nuclear Information System (INIS)

    Amin, M.H.; Ebrahimabadi, M.A.; Rahimipour, M.R.

    2009-01-01

    The effects of using nano sized carbon black in the range of 010 weight percentages on the physical and thermomechanical properties of Al 2 O 3 -Si C-SiO 2 graphite refractory composites were investigated. Nano sized carbon black addition improved the relative heat resistance and oxidation resistance of composites. The bulk density of the composites is reduced with increasing carbon black (CB) content. Increase in CB content first causes an increase in the apparent porosity, but at more than 3 wt % amount of CB, a decrease of apparent porosity was observed. The cold crushing strength (CCS) increased with increasing CB content in samples fired at 800 degree C and in samples fired at 1500 degree C when the content is increased to 3 wt %, but the CCS decreased with increasing CB content in samples fired at 1500 degree C when the CB content was less than 3 wt %. The composite without CB exhibits the highest value of CCS at firing temperature of 1500 degree C.

  12. Improved Light Conversion Efficiency Of Dye-Sensitized Solar Cell By Dispersing Submicron-Sized Granules Into The Nano-Sized TiO2 Layer

    Directory of Open Access Journals (Sweden)

    Song S.A.

    2015-06-01

    Full Text Available In this work, TiO2 nanoparticles and submicron-sized granules were synthesized by a hydrothermal method and spray pyrolysis, respectively. Submicron-sized granules were dispersed into the nano-sized TiO2 layer to improve the light conversion efficiency. Granules showed better light scattering, but lower in terms of the dye-loading quantity and recombination resistance compared with nanoparticles. Consequently, the nano-sized TiO2 layer had higher cell efficiency than the granulized TiO2 layer. When dispersed granules into the nanoparticle layer, the light scattering was enhanced without the loss of dye-loading quantities. The dispersion of granulized TiO2 led to increase the cell efficiency up to 6.51%, which was about 5.2 % higher than that of the electrode consisting of only TiO2 nanoparticles. Finally, the optimal hydrothermal temperature and dispersing quantity of granules were found to be 200°C and 20 wt%, respectively.

  13. Small angle neutron scattering study of nano sized microstructure in Fe-Cr ODS steels for gen IV in-core applications.

    Science.gov (United States)

    Han, Young-Soo; Mao, Xiadong; Jang, Jinsung

    2013-11-01

    The nano-sized microstructures in Fe-Cr oxide dispersion strengthened steel for Gen IV in-core applications were studied using small angle neutron scattering. The oxide dispersion strengthened steel was manufactured through hot isostatic pressing with various chemical compositions and fabrication conditions. Small angle neutron scattering experiments were performed using a 40 m small angle neutron scattering instrument at HANARO. Nano sized microstructures, namely, yttrium oxides and Cr-oxides were quantitatively analyzed by small angle neutron scattering. The yttrium oxides and Cr-oxides were also observed by transmission electron microscopy. The microstructural analysis results from small angle neutron scattering were compared with those obtained by transmission electron microscopy. The effects of the chemical compositions and fabrication conditions on the microstructure were investigated in relation to the quantitative microstructural analysis results obtained by small angle neutron scattering. The volume fraction of Y-oxide increases after fabrication, and this result is considered to be due to the formation of non-stochiometric Y-Ti-oxides.

  14. Effects of micro-sized and nano-sized WO_3 on mass attenauation coefficients of concrete by using MCNPX code

    International Nuclear Information System (INIS)

    Tekin, H.O.; Singh, V.P.; Manici, T.

    2017-01-01

    In the present work the effect of tungsten oxide (WO_3) nanoparticles on mass attenauation coefficients of concrete has been investigated by using MCNPX (version 2.4.0). The validation of generated MCNPX simulation geometry has been provided by comparing the results with standard XCOM data for mass attenuation coefficients of concrete. A very good agreement between XCOM and MCNPX have been obtained. The validated geometry has been used for definition of nano-WO_3 and micro-WO_3 into concrete sample. The mass attenuation coefficients of pure concrete and WO_3 added concrete with micro-sized and nano-sized have been compared. It was observed that shielding properties of concrete doped with WO_3 increased. The results of mass attenauation coefficients also showed that the concrete doped with nano-WO_3 significanlty improve shielding properties than micro-WO_3. It can be concluded that addition of nano-sized particles can be considered as another mechanism to reduce radiation dose. - Highlights: • It was found that size of the WO_3 affected the mass attenuation coefficients of concrete in all photon energies.

  15. Depositing laser-generated nanoparticles on powders for additive manufacturing of oxide dispersed strengthened alloy parts via laser metal deposition

    Science.gov (United States)

    Streubel, René; Wilms, Markus B.; Doñate-Buendía, Carlos; Weisheit, Andreas; Barcikowski, Stephan; Henrich Schleifenbaum, Johannes; Gökce, Bilal

    2018-04-01

    We present a novel route for the adsorption of pulsed laser-dispersed nanoparticles onto metal powders in aqueous solution without using any binders or surfactants. By electrostatic interaction, we deposit Y2O3 nanoparticles onto iron-chromium based powders and obtain a high dispersion of nano-sized particles on the metallic powders. Within the additively manufactured component, we show that the particle spacing of the oxide inclusion can be adjusted by the initial mass fraction of the adsorbed Y2O3 particles on the micropowder. Thus, our procedure constitutes a robust route for additive manufacturing of oxide dispersion-strengthened alloys via oxide nanoparticles supported on steel micropowders.

  16. Synthesis of nano-sized MgO particle and thin film from diethanolamine-stabilized magnesium-methoxide

    International Nuclear Information System (INIS)

    Jung, Hyun Suk; Lee, J.-K.; Young Kim, J.; Hong, Kug Sun

    2003-01-01

    The effects of diethanolamine (DEA) addition on the crystallization behavior of magnesium methoxide and the stabilization behavior of the Mg-alkoxide were investigated using differential scanning calorimetry, thermogravimetry, X-ray powder diffraction, transmission electron microscopy, and X-ray photoemission spectroscopy. 20 mol% DEA additions to magnesium methoxide showed enhanced stability such that a time-dependent change in the sol was not observed in air. Moreover, the DEA addition enhanced the crystallization process. Crystalline MgO in the 20 mol% of DEA-added magnesium methoxide powder was observed at 300 deg. C for samples processed in O 2 and a high degree of crystallinity was observed at 400 deg. C when processed in O 2 . The enhanced crystallization of Mg-methoxide with added DEA in O 2 is discussed in terms of structural relaxation and heat generation during the ignition of an organic species of DEA. Using a DEA added sol, a MgO thin film with a high degree of crystallinity was prepared at 400 deg. C in O 2

  17. The crystallinity of calcium phosphate powders influenced by the conditions of neutralized procedure with citric acid additions

    International Nuclear Information System (INIS)

    Li Chengfeng

    2009-01-01

    Calcium phosphate powders with nano-sized crystallinity were synthesized by neutralization using calcium hydroxide and orthophosphoric acid with the assistance of citric acid. The influence of processing parameters, such as free or additive citric acid, synthetic temperature and ripening time, on the crystallinity of hydroxyapatite were investigated. The results of X-ray diffraction and microstructure observations showed that the crystallinity and morphology of nano-sized hydroxyapatite particles were influenced by the presence or absence of citric acid. It was found that the crystallinities and crystallite sizes of hydroxyapatite powders prepared with the additive citric acid increased with increasing synthetic temperature and ripening time. Especially, the crystallinities of (h k 0) planes were raised and more homogeneously grown particles were obtained with increasing synthetic temperature

  18. On the efficient warm white-light emission from nano-sized Y{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Cesaria, M., E-mail: maura.cesaria@le.infn.it [Department of Mathematics and Physics “E. De Giorgi”, University of Salento, Lecce (Italy); Collins, J. [Wheaton College, Norton, MA (United States); Di Bartolo, B. [Department of Physics, Boston College, Chestnut Hill, MA (United States)

    2016-01-15

    We consider the reported emission of white light (WL) in the spectral range from 400 to beyond 900 nm induced by monochromatic infrared light (803.5 and 975 nm) continuous wave excitation of nominally un-doped yttrium oxide (Y{sub 2}O{sub 3}) nano-powders. Based on the experimental evidence, such an emission feature is a nano-scale phenomenon, resembles very closely the emission from an incandescent lamp (mimicking the sunlight, i.e., the most comfortable light to human eyes) and exhibits very high efficiency (864 lum/W) and nearly theoretical (i.e., 99) color rendering index. At the fundamental level, the origin of this phenomenon is still unexplained. In this paper we address the fundamental questions raised by the reported occurrence of WL emission from Y{sub 2}O{sub 3} nanopowders and attempt an interpretation at a more fundamental level. In particular we focus on the multiphoton-absorption and nonexponential decay patterns of the reported WL emission as starting points to formulate models and interpretations of the experimental occurrences still lacking in the literature. Our discussion invokes the electronic dispersion of Y{sub 2}O{sub 3} and nanoscale effects, which is supported by the experimental evidence according to which the observed warm WL emission is a nanoscale phenomenon with properties that only can be explained by nanoscale physics. - Highlights: • Emission of white light from 400 to beyond 900 nm induced by infrared light of un-doped Y{sub 2}O{sub 3} nano-powders. • The emission feature resembles very closely the emission from an incandescent lamp. • The observed emission properties only can be explained by nanoscale physics.

  19. Support for the initial attachment, growth and differentiation of MG-63 cells: a comparison between nano-size hydroxyapatite and micro-size hydroxyapatite in composites

    Directory of Open Access Journals (Sweden)

    Filová E

    2014-08-01

    Full Text Available Elena Filová,1 Tomáš Suchý,2,3 Zbynek Sucharda,2 Monika Šupová,2 Margit Žaloudková,2 Karel Balík,2 Vera Lisá,1 Miroslav Šlouf,4 Lucie Bacáková11Department of Biomaterials and Tissue Engineering, Institute of Physiology, 2Department of Composite and Carbon Materials, Institute of Rock Structure and Mechanics, Academy of Sciences of the Czech Republic, 3Laboratory of Biomechanics, Department of Mechanics, Biomechanics and Mechatronics, Faculty of Mechanical Engineering, CTU in Prague, 4Department of Morphology and Rheology of Polymer Materials, Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Prague, Czech RepublicAbstract: Hydroxyapatite (HA is considered to be a bioactive material that favorably influences the adhesion, growth, and osteogenic differentiation of osteoblasts. To optimize the cell response on the hydroxyapatite composite, it is desirable to assess the optimum concentration and also the optimum particle size. The aim of our study was to prepare composite materials made of polydimethylsiloxane, polyamide, and nano-sized (N or micro-sized (M HA, with an HA content of 0%, 2%, 5%, 10%, 15%, 20%, 25% (v/v (referred to as N0–N25 or M0–M25, and to evaluate them in vitro in cultures with human osteoblast-like MG-63 cells. For clinical applications, fast osseointegration of the implant into the bone is essential. We observed the greatest initial cell adhesion on composites M10 and N5. Nano-sized HA supported cell growth, especially during the first 3 days of culture. On composites with micro-size HA (2%–15%, MG-63 cells reached the highest densities on day 7. Samples M20 and M25, however, were toxic for MG-63 cells, although these composites supported the production of osteocalcin in these cells. On N2, a higher concentration of osteopontin was found in MG-63 cells. For biomedical applications, the concentration range of 5%–15% (v/v nano-size or micro-size HA seems to be optimum

  20. The effects of Ti and Sn alloying elements on precipitation strengthened Cu40Zn brass using powder metallurgy and hot extrusion

    Energy Technology Data Exchange (ETDEWEB)

    Li Shufeng, E-mail: shufenglimail@gmail.com [Joining and Welding Research Institute, Osaka University (Japan); Imai, Hisashi; Atsumi, Haruhiko; Kondoh, Katsuyoshi [Joining and Welding Research Institute, Osaka University (Japan); Kojima, Akimichi; Kosaka, Yoshiharu [San-Etsu metals Co. Ltd., 1892, OHTA, Tonami, Toyama (Japan); Yamamoto, Koji; Takahashi, Motoi [Nippon Atomized Metal Powders Corporation, 87-16, Nishi-Sangao, Noda, Chiba (Japan)

    2012-02-15

    Highlights: Black-Right-Pointing-Pointer Alloying elements Ti and Sn are proposed as additives in 60/40 brass. Black-Right-Pointing-Pointer Super-saturated Ti in powder creates high chemical potential for precipitation. Black-Right-Pointing-Pointer Ti is readily segregated in primary particle boundaries in BS40-1.0Ti. Black-Right-Pointing-Pointer Sn was proposed as an additive to inhibit segregation of Ti in BS40-1.0Ti. Black-Right-Pointing-Pointer The introduction of Sn to BS40-1.0Ti brass effectively impedes Ti segregation. - Abstract: The effects of Ti and Sn alloying elements on the microstructural and mechanical properties of 60/40 brass were studied by powder metallurgy processing. The super-saturated solid solution of Ti creates a high precipitation reaction chemical potential in water-atomized BS40-1.0Ti brass powder. Consequently, BS40-1.0Ti brass was remarkably strengthened by the addition of Ti. However, Ti readily segregated in the primary particle boundaries at elevated temperatures, which detrimentally affected the mechanical properties of BS40-1.0Ti brass. Accordingly, Sn was proposed as an additive to BS40-0.6Sn1.0Ti to inhibit the segregation of Ti. Consequently, the Ti precipitate was retained in the form of CuSn{sub 3}Ti{sub 5} in the interior of grains and grain boundaries rather than in the primary particle boundaries. This result demonstrates that the addition of Sn can effectively hinder Ti segregation in the primary particle boundaries. Sn addition produced significant grain refinement and mechanical strengthening effects in BS40-0.6Sn1.0Ti brass. As a result, outstanding strengthening effects were observed for BS40-0.6Sn1.0Ti sintered at 600 Degree-Sign C, which exhibited a yield strength of 315 MPa, an ultimate tensile strength of 598 MPa, and a Vickers micro-hardness of 216 Hv. These values represent increases of 27.5%, 20.1% and 45.6%, over those of extruded BS40-1.0Ti brass.

  1. The effects of Ti and Sn alloying elements on precipitation strengthened Cu40Zn brass using powder metallurgy and hot extrusion

    International Nuclear Information System (INIS)

    Li Shufeng; Imai, Hisashi; Atsumi, Haruhiko; Kondoh, Katsuyoshi; Kojima, Akimichi; Kosaka, Yoshiharu; Yamamoto, Koji; Takahashi, Motoi

    2012-01-01

    Highlights: ► Alloying elements Ti and Sn are proposed as additives in 60/40 brass. ► Super-saturated Ti in powder creates high chemical potential for precipitation. ► Ti is readily segregated in primary particle boundaries in BS40–1.0Ti. ► Sn was proposed as an additive to inhibit segregation of Ti in BS40–1.0Ti. ► The introduction of Sn to BS40–1.0Ti brass effectively impedes Ti segregation. - Abstract: The effects of Ti and Sn alloying elements on the microstructural and mechanical properties of 60/40 brass were studied by powder metallurgy processing. The super-saturated solid solution of Ti creates a high precipitation reaction chemical potential in water-atomized BS40-1.0Ti brass powder. Consequently, BS40–1.0Ti brass was remarkably strengthened by the addition of Ti. However, Ti readily segregated in the primary particle boundaries at elevated temperatures, which detrimentally affected the mechanical properties of BS40–1.0Ti brass. Accordingly, Sn was proposed as an additive to BS40–0.6Sn1.0Ti to inhibit the segregation of Ti. Consequently, the Ti precipitate was retained in the form of CuSn 3 Ti 5 in the interior of grains and grain boundaries rather than in the primary particle boundaries. This result demonstrates that the addition of Sn can effectively hinder Ti segregation in the primary particle boundaries. Sn addition produced significant grain refinement and mechanical strengthening effects in BS40–0.6Sn1.0Ti brass. As a result, outstanding strengthening effects were observed for BS40–0.6Sn1.0Ti sintered at 600 °C, which exhibited a yield strength of 315 MPa, an ultimate tensile strength of 598 MPa, and a Vickers micro-hardness of 216 Hv. These values represent increases of 27.5%, 20.1% and 45.6%, over those of extruded BS40–1.0Ti brass.

  2. Nano-sized Mn3O4 and β-MnOOH from the decomposition of β-cyclodextrin-Mn: 2. The water-oxidizing activities.

    Science.gov (United States)

    Najafpour, Mohammad Mahdi; Mostafalu, Ramin; Hołyńska, Małgorzata; Ebrahimi, Foad; Kaboudin, Babak

    2015-11-01

    Nano-sized Mn oxides contain Mn3O4, β-MnOOH and Mn2O3 have been prepared by a previously reported method using thermal decomposition of β-cyclodextrin-Mn complexes. In the next step, the water-oxidizing activities of these Mn oxides using cerium(IV) ammonium nitrate as a chemical oxidant are studied. The turnover frequencies for β-MnO(OH) and Mn3O4 are 0.24 and 0.01-0.17 (mmol O2/mol Mns), respectively. Subsequently, water-oxidizing activities of these compounds are compared to the other previously reported Mn oxides. Important factors affecting water oxidation by these Mn oxides are also discussed. Copyright © 2015 Elsevier B.V. All rights reserved.

  3. Effects of γ-irradiation and ageing on surface and catalytic properties of nano-sized Cu O/Mg O system

    International Nuclear Information System (INIS)

    El-Molla, S. A.; Ismail, S. A.; Ibrahim, M. M.

    2011-01-01

    0.2 Cu O/Mg O system prepared by impregnation method was calcined at 350 and 450 C. The effects of γ-rays (0.2-1.6 MGy) on its structure, surface and catalytic properties were investigated by using XRD, N 2 -adsorption at -196 C and catalytic conversion of isopropanol at 150-275 C using a flow technique. The results revealed that the investigated solids consisted of nano-sized Mg O as a major phase besides Cu O and trace amount of Cu 2 O. γ-Irradiation of the solids investigated exerted measurable changes in their surface and catalytic properties dependent on the calcination temperature and dose of irradiation. The catalysts investigated acted as active dehydrogenation solids. The five years-ageing of different solids showed limited changes of their surface and catalytic properties indicating a good catalytic stability of the irradiated prepared solids. (Author)

  4. Effects of {gamma}-irradiation and ageing on surface and catalytic properties of nano-sized Cu O/Mg O system

    Energy Technology Data Exchange (ETDEWEB)

    El-Molla, S. A. [Ain Shams University, Faculty of Education, Chemistry Deparment, Roxy, Heliopolis, 11757 Cairo (Egypt); Ismail, S. A.; Ibrahim, M. M., E-mail: saharelmolla@yahoo.com [National Center for Radiation Research and Technology, Nasr City, P.O. Box 29, 11731 Cairo (Egypt)

    2011-07-01

    0.2 Cu O/Mg O system prepared by impregnation method was calcined at 350 and 450 C. The effects of {gamma}-rays (0.2-1.6 MGy) on its structure, surface and catalytic properties were investigated by using XRD, N{sub 2}-adsorption at -196 C and catalytic conversion of isopropanol at 150-275 C using a flow technique. The results revealed that the investigated solids consisted of nano-sized Mg O as a major phase besides Cu O and trace amount of Cu{sub 2}O. {gamma}-Irradiation of the solids investigated exerted measurable changes in their surface and catalytic properties dependent on the calcination temperature and dose of irradiation. The catalysts investigated acted as active dehydrogenation solids. The five years-ageing of different solids showed limited changes of their surface and catalytic properties indicating a good catalytic stability of the irradiated prepared solids. (Author)

  5. Engineering and Scaling the Spontaneous Magnetization Reversal of Faraday Induced Magnetic Relaxation in Nano-Sized Amorphous Ni Coated on Crystalline Au.

    Science.gov (United States)

    Li, Wen-Hsien; Lee, Chi-Hung; Kuo, Chen-Chen

    2016-05-28

    We report on the generation of large inverse remanent magnetizations in nano-sized core/shell structure of Au/Ni by turning off the applied magnetic field. The remanent magnetization is very sensitive to the field reduction rate as well as to the thermal and field processes before the switching off of the magnetic field. Spontaneous reversal in direction and increase in magnitude of the remanent magnetization in subsequent relaxations over time were found. All of the various types of temporal relaxation curves of the remanent magnetizations are successfully scaled by a stretched exponential decay profile, characterized by two pairs of relaxation times and dynamic exponents. The relaxation time is used to describe the reduction rate, while the dynamic exponent describes the dynamical slowing down of the relaxation through time evolution. The key to these effects is to have the induced eddy current running beneath the amorphous Ni shells through Faraday induction.

  6. Engineering and Scaling the Spontaneous Magnetization Reversal of Faraday Induced Magnetic Relaxation in Nano-Sized Amorphous Ni Coated on Crystalline Au

    Science.gov (United States)

    Li, Wen-Hsien; Lee, Chi-Hung; Kuo, Chen-Chen

    2016-01-01

    We report on the generation of large inverse remanent magnetizations in nano-sized core/shell structure of Au/Ni by turning off the applied magnetic field. The remanent magnetization is very sensitive to the field reduction rate as well as to the thermal and field processes before the switching off of the magnetic field. Spontaneous reversal in direction and increase in magnitude of the remanent magnetization in subsequent relaxations over time were found. All of the various types of temporal relaxation curves of the remanent magnetizations are successfully scaled by a stretched exponential decay profile, characterized by two pairs of relaxation times and dynamic exponents. The relaxation time is used to describe the reduction rate, while the dynamic exponent describes the dynamical slowing down of the relaxation through time evolution. The key to these effects is to have the induced eddy current running beneath the amorphous Ni shells through Faraday induction. PMID:28773549

  7. Efficient and thermally stable red luminescence from nano-sized phosphor of Gd6MoO12:Eu3+

    International Nuclear Information System (INIS)

    Qin, Lin; Wei, Donglei; Huang, Yanlin; Kim, Sun Il; Yu, Young Moon; Seo, Hyo Jin

    2013-01-01

    A novel red-emitting nano-phosphor of Eu 3+ -doped Gd 6 MoO 12 was successfully synthesized by the Pechini method. The crystalline phase was confirmed by X-ray powder diffraction analysis. The morphology of the nano-phosphor was analyzed by scanning electron microscopy, indicating a good crystallization with particles smaller than 500 nm. The luminescence properties such as photoluminescence spectra and decay curves were investigated. The phosphors can be efficiently excited by near-ultraviolet (near-UV) light and exhibit a bright red luminescence around 613 nm ascribed to the forced electric dipole transition 5 D 0 → 7 F 2 of Eu 3+ ions. The thermal stabilities were investigated from the temperature-dependent luminescence decay curves (lifetimes) and spectra intensities. The luminescence properties in relation to applications in white light-emitting diodes (W-LEDs) such as the absolute luminescence quantum efficiency, excitation wavelength, and color coordinates were discussed. The Gd 6 MoO 12 :Eu 3+ nano-phosphor is a promising red-emitting candidate for the fabrication of W-LEDs with near-UV chips

  8. Experimental investigation and oral bioavailability enhancement of nano-sized curcumin by using supercritical anti-solvent process.

    Science.gov (United States)

    Anwar, Mohammed; Ahmad, Iqbal; Warsi, Musarrat H; Mohapatra, Sharmistha; Ahmad, Niyaz; Akhter, Sohail; Ali, Asgar; Ahmad, Farhan J

    2015-10-01

    The biomedical applications of curcumin (CUR) are limited due to its poor oral bioavailability. In this work, CUR nanoparticles were successfully prepared by combining the supercritical anti-solvent (SAS) process with Tween 80 as a solubilizing agent and permeation enhancer. Different processing parameters that can govern the mean particle size and size distribution of nanoparticles were well investigated by manipulating the types of solvents, mixing vessel pressure, mixing vessel temperature, CO2 flow rate, solution flow rate and solution concentration. Solid state characterization was done by Fourier Transform infrared spectroscopy, differential scanning calorimetry, dynamic light scattering, scanning electron microscopy, and powder X-ray diffraction study. Solubility and dissolution profile of SAS-processed CUR were found to be significantly increased in comparison with native CUR. Further, a validated ultra-performance liquid chromatographic method with quadrupole-time of flight-mass spectrometry was developed to investigate the pharmacokinetic parameters after a single oral dose (100mg/kg) administration of CUR (before/after SAS-processed) in male Wistar rats. From the plasma concentration vs. time profile graph, oral bioavailability of SAS-processed CUR was found to be increased approximately 11.6-fold (p<0.001) as compared to native CUR. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. Design and synthesis of porous nano-sized Sn@C/graphene electrode material with 3D carbon network for high-performance lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lian, Peichao, E-mail: lianpeichao@126.com [Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650500 (China); Wang, Jingyi [Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650500 (China); Cai, Dandan; Liu, Guoxue [School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640 (China); Wang, Yingying [Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650500 (China); Wang, Haihui, E-mail: hhwang@scut.edu.cn [School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640 (China)

    2014-08-01

    Highlights: • Porous nano-sized Sn@C/graphene electrode material was designed and prepared. • The preparation method presented here can avoid the agglomeration of nanoparticles. • The prepared Sn@C/graphene electrode material exhibits outstanding cyclability. - Abstract: Tin is a promising high-capacity anode material for lithium-ion batteries, but it usually suffers from the problem of poor cycling stability due to the large volume change during the charge–discharge process. In this article, porous nano-sized Sn@C/graphene electrode material with three-dimensional carbon network was designed and prepared. Reducing the size of the Sn particles to nanoscale can mitigate the absolute strain induced by the large volume change during lithiation–delithiation process, and retard particle pulverization. The porous structure can provide a void space, which helps to accommodate the volume changes of the Sn nanoparticles during the lithium uptake-release process. The carbon shell can avoid the aggregation of the Sn nanoparticles on the same piece of graphene and detachment of the pulverized Sn particles during the charge–discharge process. The 3D carbon network consisted of graphene sheets and carbon shells can not only play a structural buffering role in minimizing the mechanical stress caused by the volume change of Sn, but also keep the overall electrode highly conductive during the lithium uptake-release process. As a result, the as-prepared Sn@C/graphene nanocomposite as an anode material for lithium-ion batteries exhibited outstanding cyclability. The reversible specific capacity is almost constant from the tenth cycle to the fiftieth cycle, which is about 600 mA h g{sup −1}. The strategy presented in this work may be extended to improve the cycle performances of other high-capacity electrode materials with large volume variations during charge–discharge processes.

  10. Characterisation of micro-sized and nano-sized tungsten oxide-epoxy composites for radiation shielding of diagnostic X-rays.

    Science.gov (United States)

    Azman, N Z Noor; Siddiqui, S A; Low, I M

    2013-12-01

    Characteristics of X-ray transmissions were investigated for epoxy composites filled with 2-10 vol% WO3 loadings using synchrotron X-ray absorption spectroscopy (XAS) at 10-40 keV. The results obtained were used to determine the equivalent X-ray energies for the operating X-ray tube voltages of mammography and radiology machines. The results confirmed the superior attenuation ability of nano-sized WO3-epoxy composites in the energy range of 10-25 keV when compared to their micro-sized counterparts. However, at higher synchrotron radiation energies (i.e., 30-40 keV), the X-ray transmission characteristics were similar with no apparent size effect for both nano-sized and micro-sized WO3-epoxy composites. The equivalent X-ray energies for the operating X-ray tube voltages of the mammography unit (25-49 kV) were in the range of 15-25 keV. Similarly, for a radiology unit operating at 40-60 kV, the equivalent energy range was 25-40 keV, and for operating voltages greater than 60 kV (i.e., 70-100 kV), the equivalent energy was in excess of 40 keV. The mechanical properties of epoxy composites increased initially with an increase in the filler loading but a further increase in the WO3 loading resulted in deterioration of flexural strength, modulus and hardness. © 2013.

  11. Analysis of nano-sized irradiation-induced defects in Fe-base materials by means of small angle neutron scattering and molecular dynamics simulations

    International Nuclear Information System (INIS)

    Yu, G.

    2008-12-01

    Thermonuclear fusion of light atoms is considered since decades as an unlimited, safe and reliable source of energy that could eventually replace classical sources based on fossil fuel or nuclear fuel. Fusion reactor technology and materials studies are important parts of the fusion energy development program. For the time being, the most promising materials for structural applications in the future fusion power reactors are the Reduced Activation Ferritic/Martensitic (RAFM) steels for which the greatest technology maturity has been achieved, i.e., qualified fabrication routes, welding technology and a general industrial experience are almost available. The most important issues concerning the future use of RAFM steels in fusion power reactors are derived from their irradiation by 14 MeV neutrons that are the product, together with 3.5 MeV helium ions, of the envisaged fusion reactions between deuterium and tritium nuclei. Indeed, exposure of metallic materials to intense fluxes of 14 MeV neutrons will result in the formation of severe displacement damage (about 20-30 dpa per year) and high amounts of helium, which are at the origin of significant changes in the physical and mechanical properties of materials, such as hardening and embrittlement effects. This PhD Thesis work was aimed at investigating how far the Small Angle Neutron Scattering (SANS) technique could be used for detecting and characterizing nano-sized irradiation-induced defects in RAFM steels. Indeed, the resolution limit of Transmission Electron Microscopy (TEM) is about 1 nm in weak beam TEM imaging, and it is usually thought that a large number of irradiation-induced effects have a size below 1 nm in RAFM steels and that these very small defects actually contribute to the irradiation-induced hardening and embrittlement of RAFM steels occurring at irradiation temperatures below about 400 °C. The aim of this work was achieved by combining SANS experiments on unirradiated and irradiated specimens

  12. Magnetic and bioactivity evaluation of ferrimagnetic ZnFe{sub 2}O{sub 4} containing glass ceramics for the hyperthermia treatment of cancer

    Energy Technology Data Exchange (ETDEWEB)

    Shah, Saqlain A., E-mail: saqlain007pk@hotmail.co [Biomaterials Lab, Department of Physics, GC University Lahore (Pakistan); Hashmi, M.U. [Biomaterials Lab, Department of Physics, GC University Lahore (Pakistan); Alam, S. [PITMAEM, PCSIR Lahore (Pakistan); Shamim, A. [Biomaterials Lab, Department of Physics, GC University Lahore (Pakistan)

    2010-02-15

    Glass ceramics of the composition xZnO.25Fe{sub 2}O{sub 3}.(40-x)SiO{sub 2}.25CaO.7P{sub 2}O{sub 5}.3Na{sub 2}O were prepared by the melt-quench method using oxy-acetylene flame. Glass-powder compacts were sintered at 1100 deg. C for 3 h and then rapidly cooled at -10 deg. C. X-ray diffraction (XRD) revealed 3 prominent crystalline phases: ZnFe{sub 2}O{sub 4}, CaSiO{sub 3} and Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2}. Vibrating sample magnetometer (VSM) data at 10 KOe and 500 Oe showed that saturation magnetization, coercivity and hence hysteresis area increased with the increase in ZnO content. Nano-sized ZnFe{sub 2}O{sub 4} crystallites were of pseudo-single domain structure and thus coercivity increased with the increase in crystallite size. ZnFe{sub 2}O{sub 4} exhibited ferrimagnetism due to the random distribution of Zn{sup 2+} and Fe{sup 3+} cations at tetrahedral A sites and octahedral B sites. This inversion/random distribution of cations was probably due to the surface effects of nano-ZnFe{sub 2}O{sub 4} and rapid cooling of the material from 1100 deg. C (thus preserving the high temperature state of the random distribution of cations). Calorimetric measurements were carried out using magnetic induction furnace at 500 Oe magnetic field and 400 KHz frequency. The data showed that maximum specific power loss and temperature increase after 2 min were 26 W/g and 37 deg. C, respectively for the sample containing 10% ZnO. The samples were immersed in simulated body fluid (SBF) for 3 weeks. Scanning electron microscope (SEM), energy dispersive spectroscopy (EDX) and XRD results confirmed the growth of precipitated hydroxyapatite phase after immersion in SBF, suggesting that the ferrimagnetic glass ceramics were bioactive and could bond to the living tissues in physiological environment.

  13. Investigation of Removal Efficiency of Nano Sized Alumina for Removal of Acid Red 18 from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    M.H. Dehghani

    2014-08-01

    Full Text Available Background and Objectives: Acid Red 18 dye was one of the Azo colors that are used in textile and dyeing industries. These dyes are often toxic and carcinogenic to humans and the environment as pollution. This study was conducted with the aim of investigating on nano alumina efficiency for removal of Acid Red 18 dye from aqueous solutions. Materials and Methods: This study was carried out in the laboratory scales and effect of The initial concentration of dye (25 to 100 mg/l, pH solution (3, 7, 11, nano alumina concentration (0.1, 0.4, 1, 1.5 g/l and contact time in range 5 to 240 min on dye removal efficiency were evaluated. Also kinetic and isotherm models of adsorption process were evaluated. Results: The high removal efficiency was observed in pH=3, contact time=60 min and Adsorbent concentration of 0.4 g/L. The rate of color removal were 63/24, 50/84 and 20 percent respectively at pH of 3, 7 and 11 for the initial dye concentration of 25 mg/l and 0.4 g/l mass absorbent that showing with increasing pH removal efficiency is reduced. the studied dye absorption isotherm was fitted Langmuir model (R2=0.994 which was 83.33 mg/g for maximum adsorption. The results from kinetic studies showed that removal of the studied dye was best described by pseudo-second order kinetic model (r2=0.999. Conclusion: The present study shows nano alumina powder is promising adsorbent for removal of Acid Red 18 from aqueous solution.

  14. (YSZ) powders

    Indian Academy of Sciences (India)

    Unknown

    109–114. © Indian Academy of Sciences. 109 ... Materials Science Division, Bhabha Atomic Research Centre, Mumbai 400 085, India .... pensions of 900°C calcined YSZ powders. .... The sintered density data of the compacts (sintered at.

  15. Improvement of the mechanical properties and corrosion resistance of biodegradable β-Ca3(PO4)2/Mg-Zn composites prepared by powder metallurgy: the adding β-Ca3(PO4)2, hot extrusion and aging treatment.

    Science.gov (United States)

    Yan, Yang; Kang, Yijun; Li, Ding; Yu, Kun; Xiao, Tao; Deng, Youwen; Dai, Han; Dai, Yilong; Xiong, Hanqing; Fang, Hongjie

    2017-05-01

    In this study, 10%β-Ca 3 (PO 4 ) 2 /Mg-6%Zn (wt.%) composites with Mg-6%Zn alloy as control were prepared by powder metallurgy. After hot extrusion, the as-extruded composites were aged for 72h at 150°C. The effects of the adding β-Ca 3 (PO 4 ) 2 , hot extrusion and aging treatment on their microstructure, mechanical properties and corrosion resistance were investigated. The XRD results identified α-Mg, MgZn phase and β-Ca 3 (PO 4 ) 2 phase in these composites. After hot extrusion, grains were significantly refined, and the larger-sized β-Ca 3 (PO 4 ) 2 particles and coarse MgZn phases were broken into linear-distributed β-Ca 3 (PO 4 ) 2 and MgZn phases along the extrusion direction. After aging treatment, the elements of Zn, Ca, P and O presented a more homogeneous distribution. The compressive strengths of the β-Ca 3 (PO 4 ) 2 /Mg-Zn composites were approximately double those of natural bone, and their densities and elastic moduli matched those of natural bone. The immersion tests and electrochemical tests revealed that the adding β-Ca 3 (PO 4 ) 2 , hot extrusion and aging treatment could promote the formation of protective corrosion product layer on the sample surface in Ringer's solution, which improved corrosion resistance of the β-Ca 3 (PO 4 ) 2 /Mg-Zn composites. The XRD results indicated that the corrosion product layer contained Mg(OH) 2 , β-Ca 3 (PO 4 ) 2 and hydroxyapatite (HA). The cytotoxicity assessments showed the as-extruded β-Ca 3 (PO 4 ) 2 /Mg-Zn composite aged for 72h was harmless to L-929 cells. These results suggested that the β-Ca 3 (PO 4 ) 2 /Mg-Zn composites prepared by powder metallurgy were promising to be used for bone tissue engineering. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Synthesis of nano-sized arsenic-imprinted polymer and its use as As3+ selective ionophore in a potentiometric membrane electrode: Part 1

    International Nuclear Information System (INIS)

    Alizadeh, Taher; Rashedi, Mariyam

    2014-01-01

    Highlights: • The first arsenic cation-selective membrane electrode was introduced. • A novel procedure was introduced for the preparation of As-imprinted polymer. • It was found that arsenic is recognized by the IIP as As 3+ species. • Nernstian response of 20.4 mV decade −1 and DL of 0.5 μM was obtained. - Abstract: In this study, a new strategy was proposed for the preparation of As (III)-imprinted polymer by using arsenic (methacrylate) 3 as template. Precipitation polymerization was utilized to synthesize nano-sized As (III)-imprinted polymer. Methacrylic acid and ethylene glycol dimethacrylate were used as the functional monomer and cross-linking agent, respectively. In order to assembly functional monomers around As (III) ion, sodium arsenite and methacrylic acid were heated in the presence of hydroquinone, leading to arsenic (methacrylate) 3 . The nano-sized As (III) selective polymer was characterized by FT-IR and scanning electron microscopy techniques (SEM). It was demonstrated that arsenic was recognized as As 3+ by the selective cavities of the synthesized IIP. Based on the prepared polymer, the first arsenic cation selective membrane electrode was introduced. Membrane electrode was constructed by dispersion of As (III)-imprinted polymer nanoparticles in poly(vinyl chloride), plasticized with di-nonylphthalate. The IIP-modified electrode exhibited a Nernstian response (20.4 ± 0.5 mV decade −1 ) to arsenic ion over a wide concentration range (7.0 × 10 −7 to 1.0 × 10 −1 mol L −1 ) with a lower detection limit of 5.0 × 10 −7 mol L −1 . Unlike this, the non-imprinted polymer (NIP)-based membrane electrode was not sensitive to arsenic in aqueous solution. The selectivity of the developed sensor to As (III) was shown to be satisfactory. The sensor was used for arsenic determination in some real samples

  17. Synthesis of nano-sized arsenic-imprinted polymer and its use as As{sup 3+} selective ionophore in a potentiometric membrane electrode: Part 1

    Energy Technology Data Exchange (ETDEWEB)

    Alizadeh, Taher, E-mail: Alizadeh@uma.ac.ir; Rashedi, Mariyam

    2014-09-16

    Highlights: • The first arsenic cation-selective membrane electrode was introduced. • A novel procedure was introduced for the preparation of As-imprinted polymer. • It was found that arsenic is recognized by the IIP as As{sup 3+} species. • Nernstian response of 20.4 mV decade{sup −1} and DL of 0.5 μM was obtained. - Abstract: In this study, a new strategy was proposed for the preparation of As (III)-imprinted polymer by using arsenic (methacrylate){sub 3} as template. Precipitation polymerization was utilized to synthesize nano-sized As (III)-imprinted polymer. Methacrylic acid and ethylene glycol dimethacrylate were used as the functional monomer and cross-linking agent, respectively. In order to assembly functional monomers around As (III) ion, sodium arsenite and methacrylic acid were heated in the presence of hydroquinone, leading to arsenic (methacrylate){sub 3}. The nano-sized As (III) selective polymer was characterized by FT-IR and scanning electron microscopy techniques (SEM). It was demonstrated that arsenic was recognized as As{sup 3+} by the selective cavities of the synthesized IIP. Based on the prepared polymer, the first arsenic cation selective membrane electrode was introduced. Membrane electrode was constructed by dispersion of As (III)-imprinted polymer nanoparticles in poly(vinyl chloride), plasticized with di-nonylphthalate. The IIP-modified electrode exhibited a Nernstian response (20.4 ± 0.5 mV decade{sup −1}) to arsenic ion over a wide concentration range (7.0 × 10{sup −7} to 1.0 × 10{sup −1} mol L{sup −1}) with a lower detection limit of 5.0 × 10{sup −7} mol L{sup −1}. Unlike this, the non-imprinted polymer (NIP)-based membrane electrode was not sensitive to arsenic in aqueous solution. The selectivity of the developed sensor to As (III) was shown to be satisfactory. The sensor was used for arsenic determination in some real samples.

  18. A high gradient and strength bioseparator with nano-sized immunomagnetic particles for specific separation and efficient concentration of E. coli O157:H7

    International Nuclear Information System (INIS)

    Lin, Jianhan; Li, Min; Li, Yanbin; Chen, Qi

    2015-01-01

    Sample pretreatment is a key to rapid screening of pathogens for prevention and control of foodborne diseases. Magnetic immunoseparation is a specific method based on antibody–antigen reaction to capture the target bacteria and concentrate them in a smaller-volume buffer. The use of nano-sized magnetic particles could improve the separation efficiency of bacteria but require much higher gradient and strength magnetic field. In this study, a strong magnetic bioseparator with a mean field strength of 1.35 T and a mean gradient of 90 T/m was developed with the use of the 30 nm and 180 nm magnetic particles to specifically separate and efficiently concentrate foodborne bacterial pathogens using Escherichia coli O157:H7 as a model bacterium. The polyclonal antibodies against E. coli were evaluated using Dot ELISA analysis for their good affinity with the target bacteria and then used to modify the surface of the magnetic nanoparticles by 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) method and streptavidin-biotin binding. The magnetic particle concentrations were optimized to be 40 µg/ml and 100 µg/ml for the 30 nm and 180 nm particles, respectively, the immunoreaction time was optimized to be 45 min for both sizes of particles, and the separation times were optimized to be 60 min and 2 min for the 30 nm and 180 nm particles, respectively. The total magnetic separation time was 2 h and 1 h for the 30 nm and 180 nm particles, respectively. The experimental results demonstrated that the bioseparator with the use of either 30 nm or 180 nm immunomagnetic particles could achieve a separation efficiency of >90% for E. coli O157:H7 at the concentrations ranging from 10 2 to 10 5 cfu/ml. No obvious interferences from non-target foodborne pathogens, such as SalmonellaTyphimurium and Listeria innocua, were found. For overall consideration of the consuming time, the cost, and the separation efficiency, the 180 nm magnetic particles are practical for

  19. A high gradient and strength bioseparator with nano-sized immunomagnetic particles for specific separation and efficient concentration of E. coli O157:H7

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Jianhan, E-mail: jianhan@cau.edu.cn [Ministry of Agriculture Key Laboratory of Agricultural Information Acquisition Technology (Beijing), 17 East Tsinghua Road, China Agricultural University, Mailbox 125, Beijing 100083 (China); Li, Min [College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310058 (China); Li, Yanbin [College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310058 (China); Department of Biological and Agricultural Engineering, University of Arkansas, Fayetteville, AR 72701 (United States); Chen, Qi [Modern Precision Agriculture System Integration Research Key Laboratory of Ministry of Education, China Agricultural University, Beijing 100083 (China)

    2015-03-15

    Sample pretreatment is a key to rapid screening of pathogens for prevention and control of foodborne diseases. Magnetic immunoseparation is a specific method based on antibody–antigen reaction to capture the target bacteria and concentrate them in a smaller-volume buffer. The use of nano-sized magnetic particles could improve the separation efficiency of bacteria but require much higher gradient and strength magnetic field. In this study, a strong magnetic bioseparator with a mean field strength of 1.35 T and a mean gradient of 90 T/m was developed with the use of the 30 nm and 180 nm magnetic particles to specifically separate and efficiently concentrate foodborne bacterial pathogens using Escherichia coli O157:H7 as a model bacterium. The polyclonal antibodies against E. coli were evaluated using Dot ELISA analysis for their good affinity with the target bacteria and then used to modify the surface of the magnetic nanoparticles by 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) method and streptavidin-biotin binding. The magnetic particle concentrations were optimized to be 40 µg/ml and 100 µg/ml for the 30 nm and 180 nm particles, respectively, the immunoreaction time was optimized to be 45 min for both sizes of particles, and the separation times were optimized to be 60 min and 2 min for the 30 nm and 180 nm particles, respectively. The total magnetic separation time was 2 h and 1 h for the 30 nm and 180 nm particles, respectively. The experimental results demonstrated that the bioseparator with the use of either 30 nm or 180 nm immunomagnetic particles could achieve a separation efficiency of >90% for E. coli O157:H7 at the concentrations ranging from 10{sup 2} to 10{sup 5} cfu/ml. No obvious interferences from non-target foodborne pathogens, such as SalmonellaTyphimurium and Listeria innocua, were found. For overall consideration of the consuming time, the cost, and the separation efficiency, the 180 nm magnetic particles are

  20. A novel coating material that uses nano-sized SiO2 particles to intensify hydrophobicity and corrosion protection properties

    International Nuclear Information System (INIS)

    Ammar, Sh.; Ramesh, K.; Vengadaesvaran, B.; Ramesh, S.; Arof, A.K.

    2016-01-01

    Highlights: • Hybrid SiO 2 nanocomposite coatings were fabricated on mild steel. • Highest coating resistance were exhibited by coatings with 3 wt.% SiO 2 nanoparticles. • Long-term stability measurement, together with hydrophobic surface measurements, were obtained. - Abstract: The influence of SiO 2 nanoparticles on hydrophobicity and the corrosion protection capabilities of hybrid acrylic-silicone polymeric matrix have been investigated. Contact angle measurements (CA), atomic force microscopy (AFM), field emission scanning electron microscopy (FE-SEM), and energy dispersive X-ray spectroscopy (EDX) were used to study the hydrophobicity, morphology, and topography of the coatings. In addition, electrochemical impedance spectroscopy (EIS) and salt spray techniques were employed to evaluate the corrosion protection performance. A coating with 3 wt.% SiO 2 , AS 3, demonstrates significant improvement in corrosion resistance with the highest measured CA of 97.3°. Morphology and topography studies clarify the influence of nano-sized SiO 2 fillers on the surface topography and demonstrated the uniform and good distribution of the embedded SiO 2 nanoparticles within the polymeric matrix.

  1. QSAR analysis for nano-sized layered manganese-calcium oxide in water oxidation: An application of chemometric methods in artificial photosynthesis.

    Science.gov (United States)

    Shahbazy, Mohammad; Kompany-Zareh, Mohsen; Najafpour, Mohammad Mahdi

    2015-11-01

    Water oxidation is among the most important reactions in artificial photosynthesis, and nano-sized layered manganese-calcium oxides are efficient catalysts toward this reaction. Herein, a quantitative structure-activity relationship (QSAR) model was constructed to predict the catalytic activities of twenty manganese-calcium oxides toward water oxidation using multiple linear regression (MLR) and genetic algorithm (GA) for multivariate calibration and feature selection, respectively. Although there are eight controlled parameters during synthesizing of the desired catalysts including ripening time, temperature, manganese content, calcium content, potassium content, the ratio of calcium:manganese, the average manganese oxidation state and the surface of catalyst, by using GA only three of them (potassium content, the ratio of calcium:manganese and the average manganese oxidation state) were selected as the most effective parameters on catalytic activities of these compounds. The model's accuracy criteria such as R(2)test and Q(2)test in order to predict catalytic rate for external test set experiments; were equal to 0.941 and 0.906, respectively. Therefore, model reveals acceptable capability to anticipate the catalytic activity. Copyright © 2015 Elsevier B.V. All rights reserved.

  2. Evaluation of heavy metals in hazardous automobile shredder residue thermal residue and immobilization with novel nano-size calcium dispersed reagent.

    Science.gov (United States)

    Lee, Chi-Hyeon; Truc, Nguyen Thi Thanh; Lee, Byeong-Kyu; Mitoma, Yoshiharu; Mallampati, Srinivasa Reddy

    2015-10-15

    This study was conducted to synthesize and apply a nano-size calcium dispersed reagent as an immobilization material for heavy metal-contaminated automobile shredder residues (ASR) dust/thermal residues in dry condition. Simple mixing with a nanometallic Ca/CaO/PO4 dispersion mixture immobilized 95-100% of heavy metals in ASR dust/thermal residues (including bottom ash, cavity ash, boiler and bag filter ash). The quantity of heavy metals leached from thermal residues after treatment by nanometallic Ca/CaO/PO4 was lower than the Korean standard regulatory limit for hazardous waste landfills. The morphology and elemental composition of the nanometallic Ca/CaO-treated ASR residue were characterized by field emission scanning election microscopy combined with electron dispersive spectroscopy (FE-SEM/EDS). The results indicated that the amounts of heavy metals detectable on the ASR thermal residue surface decreased and the Ca/PO4 mass percent increased. X-ray diffraction (XRD) pattern analysis indicated that the main fraction of enclosed/bound materials on ASR residue included Ca/PO4- associated crystalline complexes, and that immobile Ca/PO4 salts remarkably inhibited the desorption of heavy metals from ASR residues. These results support the potential use of nanometallic Ca/CaO/PO4 as a simple, suitable and highly efficient material for the gentle immobilization of heavy metals in hazardous ASR thermal residue in dry condition. Copyright © 2015 Elsevier B.V. All rights reserved.

  3. Effect of Different Nano-Sized Silica Sols as Supports on the Structure and Properties of Cu/SiO2 for Hydrogenation of Dimethyl Oxalate

    Directory of Open Access Journals (Sweden)

    Chuancai Zhang

    2017-02-01

    Full Text Available Cu/x-SiO2 catalysts with 4, 10, and 20 nm silica sols as supports was produced by ammonia evaporation method and characterized. Different nano-sized silica sols as supports significantly affected the structure and catalytic properties of the copper catalysts for ethylene glycol synthesis from dimethyl oxalate. Compared with Cu/20-SiO2 and Cu/4-SiO2 catalysts, the catalytic performance and stability of Cu/10-SiO2 catalyst were greatly enhanced. The Cu/10-SiO2 catalyst showed 99.9% conversion with 94% EG selectivity and a lifetime of over 3080 h if it is calculated by industrial weight liquid hourly space velocity (WLHSV of 0.5 h−1. The Cu/10-SiO2 catalyst has one of the longest lifetimes among the catalysts and is a good alternative catalyst for this reaction. Improvement in the catalytic performance and stability of Cu/10-SiO2 is attributed to the proper SBET, Dp and larger dispersion of copper. In addition, the supports of Cu/10-SiO2 catalyst have smaller particles than that of Cu/20-SiO2; thus, the migration and growth of copper species in catalysts are restrained during the reaction.

  4. Enhanced performance of nano-sized SiC reinforced Al metal matrix nanocomposites synthesized through microwave sintering and hot extrusion techniques

    Directory of Open Access Journals (Sweden)

    M. Penchal Reddy

    2017-10-01

    Full Text Available In the present study, nano-sized SiC (0, 0.3, 0.5, 1.0 and 1.5 vol% reinforced aluminum (Al metal matrix composites were fabricated by microwave sintering and hot extrusion techniques. The structural (XRD, SEM, mechanical (nanoindentation, compression, tensile and thermal properties (co-efficient of thermal expansion-CTE of the developed Al-SiC nanocomposites were studied. The SEM/EDS mapping images show a homogeneous distribution of SiC nanoparticles into the Al matrix. A significant increase in the strength (compressive and tensile of the Al-SiC nanocomposites with the addition of SiC content is observed. However, it is noticed that the ductility of Al-SiC nanocomposites decreases with increasing volume fraction of SiC. The thermal analysis indicates that CTE of Al-SiC nanocomposites decreases with the progressive addition of hard SiC nanoparticles. Overall, hot extruded Al 1.5 vol% SiC nanocomposites exhibited the best mechanical and thermal performance as compared to the other developed Al-SiC nanocomposites. Keywords: Al-SiC nanocomposites, Microwave sintering, Hot extrusion, Mechanical properties, Thermal expansion

  5. The influence of pH and reaction time on the formation of FeSe{sub 2} upon selenite reduction by nano-sized pyrite-greigite

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Mingliang [Sun Yat-sen Univ., Zhuhai (China). Sino-French Institute of Nuclear Engineering and Technology; Bardelli, Fabrizio; Ma, Bin; Charlet, Laurent [Grenoble Univ. (France). Environmental Geochemistry Group; Chen, Fanrong; Yang, Yongqiang [Chinese Academy of Sciences, Guangzhou (China). Key Laboratory of Mineralogy and Metallogeny; Chinese Academy of Sciences, Guangzhou (China). Guangdong Provincial Key Laboratory of Mineral Physics and Materials

    2016-11-01

    The influence of pH and reaction time on the formation of FeSe{sub 2} by reductive precipitation of Se(IV) with nano-sized pyrite-greigite was investigated. Reductive precipitation is an effective method of attenuating the mobility of {sup 79}Se, which is foreseen to be a dangerous radioisotope for the geological disposal of high-level radioactive waste (HLW). The results indicated that Se(0)was formed at pH <4.05, whereas, at pH > 6.07, considerable amount of FeSe{sub 2} was formed along with Se(0). These observations are in agreement with the thermodynamic predictions reported in this work. Furthermore, the formation of FeSe{sub 2} was found to continue by increasing the reaction time, indicating that the Se(0) formed in the early reaction stage is gradually transformed to FeSe{sub 2} upon the depletion of aqueous Se(IV). Since FeSe{sub 2} has a stronger reactivity than pyrite, it was proposed that greigite, rather than pyrite, was responsible for the formation of FeSe{sub 2}. The findings in this study are of interest for key geochemical processes governing the mobility of toxic {sup 79}Se in the environment in presence of iron sulfides.

  6. Ionic conductivity and electrochemical properties of nanocomposite polymer electrolytes based on electrospun poly(vinylidene fluoride-co-hexafluoropropylene) with nano-sized ceramic fillers

    Energy Technology Data Exchange (ETDEWEB)

    Raghavan, Prasanth; Zhao Xiaohui; Kim, Jae-Kwang; Manuel, James; Chauhan, Ghanshyam S. [Department of Chemical and Biological Engineering and Engineering Research Institute, Gyeongsang National University, 900 Gajwa-dong, Jinju 660-701 (Korea, Republic of); Ahn, Jou-Hyeon [Department of Chemical and Biological Engineering and Engineering Research Institute, Gyeongsang National University, 900 Gajwa-dong, Jinju 660-701 (Korea, Republic of)], E-mail: jhahn@gnu.ac.kr; Nah, Changwoon [Department of Polymer-Nano Science and Technology, Chonbuk National University, 664-14 Duckjin-dong, Jeonju 561-756 (Korea, Republic of)

    2008-12-30

    A series of nanocomposite polymer electrolytes (NCPEs) comprising nanoparticles of BaTiO{sub 3}, Al{sub 2}O{sub 3} or SiO{sub 2} were prepared by electrospinning technique. The nano-sized ceramic fillers were incorporated into poly(vinylidene fluoride-co-hexafluoropropylene) [P(VdF-HEP)] membranes during the electrospinning process. The resultant porous membranes are good absorbent of the liquid electrolyte and exhibit high electrolyte retention capacity. The presence of the ceramic nanoparticles has positive effect on the mechanical properties of the membranes. The ionic conductivity and the electrochemical stability window of the electrospun P(VdF-HFP)-based polymer are enhanced by the presence of the fillers. The cell Li/LiFePO{sub 4} based on the NCPE containing BaTiO{sub 3} delivers a discharge capacity of 164 mAh/g, which corresponds to 96.5% utilization of the active material. In comparison, the performance of Li/LiFePO{sub 4} cells with NCPEs containing Al{sub 2}O{sub 3} and SiO{sub 2} was observed to be lower with respective discharge capacities of 153 and 156 mAh/g. The enhanced performance of the BaTiO{sub 3}-based-NCPE is attributed mainly to its better interaction with the host polymer and compatibility with lithium metal.

  7. Polyether ether ketone implants achieve increased bone fusion when coated with nano-sized hydroxyapatite: a histomorphometric study in rabbit bone.

    Science.gov (United States)

    Johansson, Pär; Jimbo, Ryo; Naito, Yoshihito; Kjellin, Per; Currie, Fredrik; Wennerberg, Ann

    2016-01-01

    Polyether ether ketone (PEEK) possesses excellent mechanical properties similar to those of human bone and is considered the best alternative material other than titanium for orthopedic spine and trauma implants. However, the deficient osteogenic properties and the bioinertness of PEEK limit its fields of application. The aim of this study was to limit these drawbacks by coating the surface of PEEK with nano-scaled hydroxyapatite (HA) minerals. In the study, the biological response to PEEK, with and without HA coating, was investigated. Twenty-four screw-like and apically perforated implants in the rabbit femur were histologically evaluated at 3 weeks and 12 weeks after surgery. Twelve of the 24 implants were HA coated (test), and the remaining 12 served as uncoated PEEK controls. At 3 weeks and 12 weeks, the mean bone-implant contact was higher for test compared to control (P<0.05). The bone area inside the threads was comparable in the two groups, but the perforating hole showed more bone area for the HA-coated implants at both healing points (P<0.01). With these results, we conclude that nano-sized HA coating on PEEK implants significantly improved the osteogenic properties, and in a clinical situation this material composition may serve as an implant where a rapid bone fusion is essential.

  8. Comparative study of nano-sized particles CoFe{sub 2}O{sub 4} effects on superconducting properties of Y-123 and Y-358

    Energy Technology Data Exchange (ETDEWEB)

    Slimani, Y.; Hannachi, E.; Ben Salem, M.K.; Hamrita, A. [Laboratory of Physics of Materials-Structures and Properties, Department of Physics, Faculty of Sciences of Bizerte, University of Carthage, 7021 Zarzouna (Tunisia); Varilci, A. [Faculty of Arts and Sciences, Department of Physics, Abant Izzet Baysal University, 14280 Bolu (Turkey); Dachraoui, W. [CINaM-CNRS, Luminy Campus, 13288 Marseille (France); Ben Salem, M., E-mail: salemwiem2005@yahoo.fr [Laboratory of Physics of Materials-Structures and Properties, Department of Physics, Faculty of Sciences of Bizerte, University of Carthage, 7021 Zarzouna (Tunisia); Ben Azzouz, F. [Laboratory of Physics of Materials-Structures and Properties, Department of Physics, Faculty of Sciences of Bizerte, University of Carthage, 7021 Zarzouna (Tunisia); College of Sciences-Girls, Department of Physics, University of Dammam (Saudi Arabia)

    2014-10-01

    The effects of nano-sized CoFe{sub 2}O{sub 4} particles (10 nm) addition on the structural and the normal state resistivity of YBa{sub 2}Cu{sub 3}O{sub 7} (noted Y-123) and Y{sub 3}Ba{sub 5}Cu{sub 8}O{sub 18} (noted Y-358) polycrystalline were systematically studied. Samples were synthesized in oxygen atmosphere using a standard solid state reaction technique by adding CoFe{sub 2}O{sub 4} up to 2 wt%. Phases, microstructure and superconductivity have been systematically investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrical measurements ρ(T). XRD results reveal that the lattice parameters change for both Y-123 and Y-358 phases. SEM observations reveal that the grain size is reduced with increasing the content of CoFe{sub 2}O{sub 4}. The measurements for the resistivity dependence of temperature show that the depression in superconducting temperature is more pronounced for CoFe{sub 2}O{sub 4} addition in Y-358 compound than in Y-123 one. These results may be attributed to the existence of much more disorder due to a greater number of Cu sites to be substituted by Fe and Co in Y-358 compared to Y-123.

  9. Adsorption and Desorption Characteristics of Cd2+ and Pb2+ by Micro and Nano-sized Biogenic CaCO3

    Science.gov (United States)

    Liu, Renlu; Guan, Yong; Chen, Liang; Lian, Bin

    2018-01-01

    The purpose of this study was to elucidate the characteristics and mechanisms of adsorption and desorption for heavy metals by micro and nano-sized biogenic CaCO3 induced by Bacillus subtilis, and the pH effect on adsorption was investigated. The results showed that the adsorption characteristics of Cd2+ and Pb2+ are well described by the Langmuir adsorption isothermal equation, and the maximum adsorption amounts for Cd2+ and Pb2+ were 94.340 and 416.667 mg/g, respectively. The maximum removal efficiencies were 97% for Cd2+, 100% for Pb2+, and the desorption rate was smaller than 3%. Further experiments revealed that the biogenic CaCO3 could maintain its high adsorption capability for heavy metals within wide pH ranges (3–8). The FTIR and XRD results showed that, after the biogenic CaCO3 adsorbed Cd2+ or Pb2+, it did not produce a new phase, which indicated that biogenic CaCO3 and heavy metal ions were governed by a physical adsorption process, and the high adsorptive capacity of biogenic CaCO3 for Cd2+ and Pb2+ were mainly attributed to its large total specific surface area. The findings could improve the state of knowledge about biogenic CaCO3 formation in the environment and its potential roles in the biogeochemical cycles of heavy metals. PMID:29434577

  10. Study of chemically synthesized ZnO nano particles under a bio template using radioactive ion beam

    CERN Multimedia

    This is a project proposal to study nano sized semiconductor ZnO system, useful in biology and medicinal purposes, using radioactive ion beam from ISOLDE. Doping of the nano particles with Cu, Cd and Ga ions (in their variable valancy states) are expected to impart changes in the electrical structure and properties in the said system under study. The morphological changes, chemical environment, micro structure, electrical and optical properties of the nano size particles of ZnO system (developed under a bio template of folic acid) after the interaction with radioactive ion beam will be studied. The provision of perturbed angular correlation (PAC) study with respect to the changes in chemical environment, where ever possible will be attempted.

  11. Competing effects between intrinsic and extrinsic defects in pure and Mn-doped ZnO nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Ruf, Thomas; Repp, Sergej; Urban, Joanna [Albert-Ludwigs-Universität Freiburg, Institut für Physikalische Chemie (Germany); Thomann, Ralf [Albert-Ludwigs-Universität Freiburg, Freiburger Materialforschungszentrum (FMF) (Germany); Erdem, Emre, E-mail: emre.erdem@physchem.uni-freiburg.de [Albert-Ludwigs-Universität Freiburg, Institut für Physikalische Chemie (Germany)

    2016-05-15

    Nano-sized ZnO doped with transition metals is one of the most promising candidates in the field of diluted magnetic semiconductors unifying ferromagnetic and semiconductor properties. Promising is the exploitation of the magnetic spin of the electron and by that the application in spintronics. As the mechanism of spin coupling is still controversial, insight into the coexistence and interaction of intrinsic and extrinsic effects is vital for further technological progress. We report on the synthesis of a set of nano-sized Zn{sub 1−x}Mn{sub x}O samples with a nominal concentration of x = 0.000005–0.03 and structural (XRD, TEM, and AFM), as well as electronic (PL, UV–Vis, FTIR, and EPR) investigations. In this contribution, possible interaction effects were summarized in terms of Mn doping and size. PL quenching after doping was also discussed as another aspect for the interrelations of the defects.

  12. Characterization and Influence of Green Synthesis of Nano-Sized Zinc Complex with 5-Aminolevulinic Acid on Bioactive Compounds of Aniseed.

    Science.gov (United States)

    Tavallali, Vahid; Rahmati, Sadegh; Rowshan, Vahid

    2017-11-01

    A new water soluble zinc-aminolevulinic acid nano complex (n[Zn(ALA) 2 ]), which was characterized by TEM, IR, and EDX spectra, has been prepared via sonochemical method under green conditions in water. In the current study, the effectiveness of foliar Zn amendment using synthetic Zn-ALA nano complex, as a new introduced Zn-fertilizer here, was evaluated. As the model plant, Pimpinella anisum, the most valuable spice and medicinal plant grown in warm regions, was used. By using zinc nano complex, further twenty compounds were obtained in the essential oil of anise plants. Application of 0.2% (w/v) Zn-ALA nano complex increased the levels of (E)-anethole, β-bisabolene, germacrene D, methyl chavicol, and α-zingiberene in the essential oil. Nano Zn complex at the rate of 0.2% induced considerable high phenolic compounds and zinc content of shoots and seeds. Chlorogenic acid had the highest level between four detected phenolic compounds. The maximum antioxidant activity was monitored through the application of Zn nano complex. According to the results, nanoscale nutrients can be provided with further decreased doses for medicinal plants. Using Zn-ALA nano complex is a new and efficient method to improve the pharmaceutical and food properties of anise plants. © 2017 Wiley-VHCA AG, Zurich, Switzerland.

  13. Powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Hart, M.

    1995-12-31

    the importance of x-ray powder diffraction as an analytical tool for phase identification of materials was first pointed out by Debye and Scherrer in Germany and, quite independently, by Hull in the US. Three distinct periods of evolution lead to ubiquitous application in many fields of science and technology. In the first period, until the mid-1940`s, applications were and developed covering broad categories of materials including inorganic materials, minerals, ceramics, metals, alloys, organic materials and polymers. During this formative period, the concept of quantitative phase analysis was demonstrated. In the second period there followed the blossoming of technology and commercial instruments became widely used. The history is well summarized by Parrish and by Langford and Loueer. By 1980 there were probably 10,000 powder diffractometers in routine use, making it the most widely used of all x-ray crystallographic instruments. In the third, present, period data bases became firmly established and sophisticated pattern fitting and recognition software made many aspects of powder diffraction analysis routine. High resolution, tunable powder diffractometers were developed at sources of synchrotron radiation. The tunability of the spectrum made it possible to exploit all the subtleties of x-ray spectroscopy in diffraction experiments.

  14. Powder diffraction

    International Nuclear Information System (INIS)

    Hart, M.

    1995-01-01

    The importance of x-ray powder diffraction as an analytical tool for phase identification of materials was first pointed out by Debye and Scherrer in Germany and, quite independently, by Hull in the US. Three distinct periods of evolution lead to ubiquitous application in many fields of science and technology. In the first period, until the mid-1940's, applications were and developed covering broad categories of materials including inorganic materials, minerals, ceramics, metals, alloys, organic materials and polymers. During this formative period, the concept of quantitative phase analysis was demonstrated. In the second period there followed the blossoming of technology and commercial instruments became widely used. The history is well summarized by Parrish and by Langford and Loueer. By 1980 there were probably 10,000 powder diffractometers in routine use, making it the most widely used of all x-ray crystallographic instruments. In the third, present, period data bases became firmly established and sophisticated pattern fitting and recognition software made many aspects of powder diffraction analysis routine. High resolution, tunable powder diffractometers were developed at sources of synchrotron radiation. The tunability of the spectrum made it possible to exploit all the subtleties of x-ray spectroscopy in diffraction experiments

  15. Powder diffractometry

    International Nuclear Information System (INIS)

    Doucet, J.

    1983-01-01

    The new possibilities openned by the synchrotron radiation in the powder diffractometry techniques are presented. This technique is described in a general manner and some aspects which can be developed with the use of the synchrotron radiation are analyzed. (L.C.) [pt

  16. Spark plasma sintering of TiNi nano-powders for biological application

    International Nuclear Information System (INIS)

    Fu, Y Q; Gu, Y W; Shearwood, C; Luo, J K; Flewitt, A J; Milne, W I

    2006-01-01

    Nano-sized TiNi powder with an average size of 50 nm was consolidated using spark plasma sintering (SPS) at 800 deg. C for 5 min. A layer of anatase TiO 2 coating was formed on the sintered TiNi by chemical reaction with a hydrogen peroxide (H 2 O 2 ) solution at 60 deg. C followed by heat treatment at 400 deg. C to enhance the bioactivity of the metal surface. Cell culture using osteoblast cells and a biomimetic test in simulated body fluid proved the biocompatibility of the chemically treated SPS TiNi

  17. Synthesis of Nano sized Zinc-Doped Cobalt Oxyhydroxide Parties by a Dropping Method and Their Carbon Monoxide Gas Sensing Properties

    International Nuclear Information System (INIS)

    Wang, J.W.; Kuo, Y.M.

    2013-01-01

    Two nano structures of cobalt oxyhydroxide (CoOOH) and Zinc-(Zn-) doped CoOOH (1–4% Zn) are prepared from Co(NO 3 ) 2 solution via microtitration with NaOH and oxidation in air. The X-ray diffraction (XRD) analysis results show that a pure state of nano-CoOOH can be obtained at an alkalinity (OH−/Co + ) of 5 with 40°C heat treatment after 6 h. The Zn ions preferentially substitute Co ions in the CoOOH structure, resulting in a decrease of its crystallinity. The disc-like CoOOH nano structure exhibits good sensitivity to carbon monoxide (CO) in a temperature range of 40–110°C with maximum sensitivity to CO at around 70–80°C. When CoOOH nano structure is doped with 1% Zn, its sensitivity and selectivity for CO gas are improved at 70–80°C; further Zn doping to 2% degraded the CO sensing properties of nano-CoOOH. The results of a cross-sensitivity investigation of the sensor to various gases coexisting at early stages of a fire show that the sensitivity of Zn-doped nano-CoOOH is the highest toward CO. Zn-doped nano-CoOOH film exhibits a high sensitivity to CO at room temperature, making it a promising sensor for early-stage fire detection.

  18. Highly selective solid phase extraction and preconcentration of Azathioprine with nano-sized imprinted polymer based on multivariate optimization and its trace determination in biological and pharmaceutical samples

    International Nuclear Information System (INIS)

    Davarani, Saied Saeed Hosseiny; Rezayati zad, Zeinab; Taheri, Ali Reza; Rahmatian, Nasrin

    2017-01-01

    In this research, for first time selective separation and determination of Azathioprine is demonstrated using molecularly imprinted polymer as the solid-phase extraction adsorbent, measured by spectrophotometry at λ max 286 nm. The selective molecularly imprinted polymer was produced using Azathioprine and methacrylic acid as a template molecule and monomer, respectively. A molecularly imprinted solid-phase extraction procedure was performed in column for the analyte from pharmaceutical and serum samples. The synthesized polymers were characterized by infrared spectroscopy (IR), field emission scanning electron microscopy (FESEM). In order to investigate the effect of independent variables on the extraction efficiency, the response surface methodology (RSM) based on Box–Behnken design (BBD) was employed. The analytical parameters such as precision, accuracy and linear working range were also determined in optimal experimental conditions and the proposed method was applied to analysis of Azathioprine. The linear dynamic range and limits of detection were 2.5–0.01 and 0.008 mg L ‐1 respectively. The recoveries for analyte were higher than 95% and relative standard deviation values were found to be in the range of 0.83–4.15%. This method was successfully applied for the determination of Azathioprine in biological and pharmaceutical samples. - Graphical abstract: A new-nano sized imprinted polymer was synthesized and applied as sorbent in SPE in order to selective recognition, preconcentration, and determination of Azathioprine with the response surface methodology based on Box–Behnken design and was successfully investigated for the clean-up of human blood serum and pharmaceutical samples. - Highlights: • The nanosized-imprinted polymer has been synthesized by precipitation polymerization technique. • A molecularly imprinted solid-phase extraction procedure was performed for determination of Azathioprine. • The Azathioprine-molecular imprinting

  19. The role of stable interface in nano-sized FeNbO4 as anode electrode for lithium-ion batteries

    International Nuclear Information System (INIS)

    Wang, Ting; Shi, Shaojun; Kong, Fanjun; Yang, Gang; Qian, Bin; Yin, Fan

    2016-01-01

    Graphical abstract: After dozens of charge/discharge cycles, the electrode of Nano-FNO remains the homogeneous combination with active material and conductive carbon, but the microcrystals in Micro-FNO electrode are cracked to small particles. The pulverization of Micro-FNO not only blocks the transfer of Li + and electrons due to the separation of the active material and conductive carbon, but also results in the falling of active material from the current collector. Nano-FNO can remain the excellent capacity after dozens of cycles. - Abstract: Nano-sized FeNbO 4 (Nano-FNO) with an average diameter of 120 nm is facilely prepared by co-precipitation method. Bulk FeNbO 4 (Micro-FNO) as a comparison synthesized by conventional solid-state synthesis has an average grain size of 3–10 μm. In the high-resolution transmission electron microscopy (HRTEM) images, Nano-FNO reveals an ordered single crystal structure, but Mirco-FNO is composed of disordered crystallites with different crystal orientation. Nano-FNO as anode material delivers the initial capacity of 475 mAh g −1 which is much higher than Micro-FNO electrode of 250 mAh g −1 .After dozens of charge/discharge cycles, the electrode of Nano-FNO remains the homogeneous combination with active material and conductive carbon, but the microcrystals in Micro-FNO electrode are cracked to small particles. The pulverization of Micro-FNO not only blocks the transfer of Li + and electrons due to the separation between the active material and conductive carbon, but also results in the falling of active material from the current collector. Compared with the weakened electrochemical performances of Micro-FNO, Nano-FNO remains the excellent capacity after dozens of cycles. The charge transfer resistances of Nano-FNO and Micro-FNO after several cycles are further studied by fitting their electrochemical impedance spectra.

  20. Nano-Sized Secondary Organic Aerosol of Diesel Engine Exhaust Origin Impairs Olfactory-Based Spatial Learning Performance in Preweaning Mice

    Directory of Open Access Journals (Sweden)

    Tin-Tin Win-Shwe

    2015-06-01

    Full Text Available The aims of our present study were to establish a novel olfactory-based spatial learning test and to examine the effects of exposure to nano-sized diesel exhaust-origin secondary organic aerosol (SOA, a model environmental pollutant, on the learning performance in preweaning mice. Pregnant BALB/c mice were exposed to clean air, diesel exhaust (DE, or DE-origin SOA (DE-SOA from gestational day 14 to postnatal day (PND 10 in exposure chambers. On PND 11, the preweaning mice were examined by the olfactory-based spatial learning test. After completion of the spatial learning test, the hippocampus from each mouse was removed and examined for the expressions of neurological and immunological markers using real-time RT-PCR. In the test phase of the study, the mice exposed to DE or DE-SOA took a longer time to reach the target as compared to the control mice. The expression levels of neurological markers such as the N-methyl-d-aspartate (NMDA receptor subunits NR1 and NR2B, and of immunological markers such as TNF-α, COX2, and Iba1 were significantly increased in the hippocampi of the DE-SOA-exposed preweaning mice as compared to the control mice. Our results indicate that DE-SOA exposure in utero and in the neonatal period may affect the olfactory-based spatial learning behavior in preweaning mice by modulating the expressions of memory function–related pathway genes and inflammatory markers in the hippocampus.

  1. Development of a Sensitive Electrochemical Enzymatic Reaction-Based Cholesterol Biosensor Using Nano-Sized Carbon Interdigitated Electrodes Decorated with Gold Nanoparticles.

    Science.gov (United States)

    Sharma, Deepti; Lee, Jongmin; Seo, Junyoung; Shin, Heungjoo

    2017-09-15

    We developed a versatile and highly sensitive biosensor platform. The platform is based on electrochemical-enzymatic redox cycling induced by selective enzyme immobilization on nano-sized carbon interdigitated electrodes (IDEs) decorated with gold nanoparticles (AuNPs). Without resorting to sophisticated nanofabrication technologies, we used batch wafer-level carbon microelectromechanical systems (C-MEMS) processes to fabricate 3D carbon IDEs reproducibly, simply, and cost effectively. In addition, AuNPs were selectively electrodeposited on specific carbon nanoelectrodes; the high surface-to-volume ratio and fast electron transfer ability of AuNPs enhanced the electrochemical signal across these carbon IDEs. Gold nanoparticle characteristics such as size and morphology were reproducibly controlled by modulating the step-potential and time period in the electrodeposition processes. To detect cholesterol selectively using AuNP/carbon IDEs, cholesterol oxidase (ChOx) was selectively immobilized via the electrochemical reduction of the diazonium cation. The sensitivity of the AuNP/carbon IDE-based biosensor was ensured by efficient amplification of the redox mediators, ferricyanide and ferrocyanide, between selectively immobilized enzyme sites and both of the combs of AuNP/carbon IDEs. The presented AuNP/carbon IDE-based cholesterol biosensor exhibited a wide sensing range (0.005-10 mM) and high sensitivity (~993.91 µA mM -1 cm -2 ; limit of detection (LOD) ~1.28 µM). In addition, the proposed cholesterol biosensor was found to be highly selective for the cholesterol detection.

  2. Activating antioxidant enzymes, hyoscyamine and scopolamine biosynthesis of Hyoscyamus niger L. plants with nano-sized titanium dioxide and bulk application

    Directory of Open Access Journals (Sweden)

    Mansour GHORBANPOUR

    2015-11-01

    Full Text Available  Application of nanotechnology is now widely distributed overall the life, especially in agricultural systems. This study intended to indicate the impacts of nano-sized titanium dioxide particles (NT and bulk (BT on antioxidant enzymes activities including superoxide dismutase (SOD, peroxidase (POX and catalase (CAT, and variations of two major tropane alkaloids such as hyoscyamine (HYO and scopolamine (SCO in Hyoscyamus niger L. Plants were treated with different concentrations of NT and BT (0, 20, 40 and 80 mg l-1. Alkaloids extracted were identified by gas chromatography (GC and gas chromatography-mass spectrometry (GC-MS analysis. Results showed that SOD activity increased with increasing titanium dioxide concentration in both nano-particles and bulk treated plants. However, the highest and the lowest POX activity were observed in plants exposed to NT at 40 mg l-1 and control, respectively. Generally, all tested enzymes activities were higher in NT treated plants that those of BT except CAT activity at 80 mg l-1. The highest alkaloids content values, HYO: 0.286 g kg-1 and SCO: 0.126 g kg-1, were achieved in plants treated with NT at 80 and 20 mg l-1, respectively. The maximum and minimum plant biomass and subsequently total alkaloids yield were obtained in plants exposed to NT at 40 mg l-1 and controls, respectively. Our results suggest that NT in appropriate level (40 mg l-1 may act as an elicitor for biochemical responses and tropane alkaloids biosynthesis in H. niger plants. 

  3. Polyether ether ketone implants achieve increased bone fusion when coated with nano-sized hydroxyapatite: a histomorphometric study in rabbit bone

    Directory of Open Access Journals (Sweden)

    Johansson P

    2016-04-01

    Full Text Available Pär Johansson,1 Ryo Jimbo,1 Yoshihito Naito,2 Per Kjellin,3 Fredrik Currie,3 Ann Wennerberg1 1Department of Prosthodontics, Faculty of Odontology, Malmö University, Malmö, Sweden; 2Oral Implant Center, Tokushima University Hospital, Tokushima, Japan; 3Promimic AB, Stena Center, Göteborg, Sweden Abstract: Polyether ether ketone (PEEK possesses excellent mechanical properties similar to those of human bone and is considered the best alternative material other than titanium for orthopedic spine and trauma implants. However, the deficient osteogenic properties and the bioinertness of PEEK limit its fields of application. The aim of this study was to limit these drawbacks by coating the surface of PEEK with nano-scaled hydroxyapatite (HA minerals. In the study, the biological response to PEEK, with and without HA coating, was investigated. Twenty-four screw-like and apically perforated implants in the rabbit femur were histologically evaluated at 3 weeks and 12 weeks after surgery. Twelve of the 24 implants were HA coated (test, and the remaining 12 served as uncoated PEEK controls. At 3 weeks and 12 weeks, the mean bone–implant contact was higher for test compared to control (P<0.05. The bone area inside the threads was comparable in the two groups, but the perforating hole showed more bone area for the HA-coated implants at both healing points (P<0.01. With these results, we conclude that nano-sized HA coating on PEEK implants significantly improved the osteogenic properties, and in a clinical situation this material composition may serve as an implant where a rapid bone fusion is essential. Keywords: HA, PEEK, osseointegration, histology, orthopedics, in vivo

  4. Voltammetric determination of ultratrace levels of cerium(III) using a carbon paste electrode modified with nano-sized cerium-imprinted polymer and multiwalled carbon nanotubes

    International Nuclear Information System (INIS)

    Alizadeh, Taher; Ganjali, Mohammad Reza; Akhoundian, Maede; Norouzi, Parviz

    2016-01-01

    A carbon paste electrode was modified with a Ce(III)-imprinted polymer (Ce-IP) and used for voltammetric determination of Ce(III) ions in real water samples. Precipitation polymerization was used for synthesis of the nano-sized Ce-IP from vinylpyridine and methacrylic acid (acting as the complexing ligands and functional monomers), divinylbenzene (cross-linker) and AIBN as the radical starter. The Ce-IP was characterized by scanning electron microscopy and zeta potentials. A carbon paste electrode (CPE) was then impregnated with the Ce-IP and used for the extraction and subsequent determination of Ce(III). Oxidative square wave voltammetry showed the electrode to give a significantly better response than an electrode modified with the non-imprinted polymer. The addition of multiwalled carbon nanotubes to the Ce-IP-modified electrode further improves the signal, thereby increasing the sensitivity of the method. The effects of electrode composition, extraction pH value, volume and time were optimized. The electrode, if operated at a voltage of 1.05 V (vs. Ag/AgCl), displays a linear response to Ce(III) in the 1.0 μM to 25 pM concentration range, and the detection limit is 10 pM (at an S/N ratio of 3). The relative standard deviation of 5 separate determinations is 3.1 %. The method was successfully applied to the determination of Ce(III) in the spiked samples of drinking water and sea water. (author)

  5. Potential of laser-induced breakdown spectroscopy for discrimination of nano-sized carbon materials. Insights on the optical characterization of graphene

    Energy Technology Data Exchange (ETDEWEB)

    Serrano, J.; Cabalín, L.M.; Moros, J.; Laserna, J.J., E-mail: laserna@uma.es

    2014-07-01

    Since its invention in 2004, graphene has attracted considerable interest worldwide. Advances in the use of graphene in materials science and engineering require important increases in the quality of the final product for integration in photonic and electronic devices. To meet this demand, which will become increasingly strict in the future, analytical techniques capable of differentiating between the starting materials and graphene need to be developed. The interest in the use of laser-induced breakdown spectroscopy (LIBS) for this application rests on the rapid progress experienced by this technology for identification of carbon-based materials of close chemical composition. The potential of LIBS has been explored here by a careful investigation of the spectral properties of both multi-layer and few-layer graphene, graphite and graphene oxide. Results reveal significant differences in the specific optical emission responses of these materials, expressly reflected on the behavior of CN and C{sub 2} molecular emissions. These differences result from the particularities of the materials, such as the number of carbon layers and the carbon hybridization in the bonding structure, together with the post-ablation evolution of the concerned plasma plume. In short, this interconnection between ablation and emission events generated from each material allows its characterization and its differentiation from other materials with highly similar chemical composition. - Highlights: • The emitting behavior of nano-sized carbon lattices has been evaluated. • Laser fluence change impacts equally on optical emissions from pure carbon lattices. • Temporal profiles of molecular emissions reveal differences between carbon lattices. • Variable stacking of nano-carbon layers leads to difference in molecular emissions.

  6. Compression Properties and Electrical Conductivity of In-Situ 20 vol.% Nano-Sized TiCx/Cu Composites with Different Particle Size and Morphology.

    Science.gov (United States)

    Zhang, Dongdong; Bai, Fang; Sun, Liping; Wang, Yong; Wang, Jinguo

    2017-05-04

    The compression properties and electrical conductivity of in-situ 20 vol.% nano-sized TiC x /Cu composites fabricated via combustion synthesis and hot press in Cu-Ti-CNTs system at various particles size and morphology were investigated. Cubic-TiC x /Cu composite had higher ultimate compression strength (σ UCS ), yield strength (σ 0.2 ), and electric conductivity, compared with those of spherical-TiC x /Cu composite. The σ UCS , σ 0.2 , and electrical conductivity of cubic-TiC x /Cu composite increased by 4.37%, 20.7%, and 17.8% compared with those of spherical-TiC x /Cu composite (526 MPa, 183 MPa, and 55.6% International Annealed Copper Standard, IACS). Spherical-TiC x /Cu composite with average particle size of ~94 nm exhibited higher ultimate compression strength, yield strength, and electrical conductivity compared with those of spherical-TiC x /Cu composite with 46 nm in size. The σ UCS , σ 0.2 , and electrical conductivity of spherical-TiC x /Cu composite with average size of ~94 nm in size increased by 17.8%, 33.9%, and 62.5% compared with those of spherical-TiC x /Cu composite (417 MPa, 121 MPa, and 40.3% IACS) with particle size of 49 nm, respectively. Cubic-shaped TiC x particles with sharp corners and edges led to stress/strain localization, which enhanced the compression strength of the composites. The agglomeration of spherical-TiC x particles with small size led to the compression strength reduction of the composites.

  7. Effects of nano-sized zero-valent iron (nZVI) on DDT degradation in soil and its toxicity to collembola and ostracods.

    Science.gov (United States)

    El-Temsah, Yehia S; Joner, Erik J

    2013-06-01

    Nano-sized zero valent iron (nZVI) has been studied for in situ remediation of contaminated soil and ground water. However, little is known about its effects on organisms in soil and aquatic ecosystems. In this study, the effect of nZVI on degradation of DDT and its ecotoxicological effects on collembola (Folsomia candida) and ostracods (Heterocypris incongruens) were investigated. Two soils were used in suspension incubation experiments lasting for 7 and 30 d; a spiked (20 mg DDT kg(-1)) sandy soil and an aged (>50 years) DDT-polluted soil (24 mg DDT kg(-1)). These were incubated with 1 or 10 g nZVI kg(-1), and residual toxicity in soil and the aqueous phase tested using ecotoxicological tests with collembola or ostracods. Generally, addition of either concentration of nZVI to soil led to about 50% degradation of DDT in spiked soil at the end of 7 and 30 d incubation, while the degradation of DDT was less in aged DDT-polluted soil (24%). Severe negative effects of nZVI were observed on both test organisms after 7 d incubation, but prolonged incubation led to oxidation of nZVI which reduced its toxic effects on the tested organisms. On the other hand, DDT had significant negative effects on collembolan reproduction and ostracod development. We conclude that 1 g nZVI kg(-1) was efficient for significant DDT degradation in spiked soil, while a higher concentration was necessary for treating aged pollutants in soil. The adverse effects of nZVI on tested organisms seem temporary and reduced after oxidation. Copyright © 2013 Elsevier Ltd. All rights reserved.

  8. Examination of Zinc Oxide Nanoparticles as a Fluorescent Fingerprint Detection Powder

    International Nuclear Information System (INIS)

    Tun Tun Lin

    2010-12-01

    Detection of latent fingerprint was performed using zinc oxide nanoparticles which were produced by simple and efficient method in aqueous media from zinc nitrate. Synthesized ZnO nanoparticles were characterized by XRD, SEM and AFM for ZnO purification and particle size examination. In this paper an effort has been made to compare the results of using ZnO nanoparticles and conventional fingerprint powders such as ZnO bulk powder, CaO, TiO2, printer toner powder and graphite. Fingerprints on different materials were also examined by the use of ZnO and Graphite powder, which is currently used in the Central Intelligence Department of Myanmar Police Force.From this research, it was observed that zinc oxide nanoparticles powder produced a much clearer picture of the fingerprints, compared to conventional powders and it has very good quality at sticking to the fingerprint residue but not to the background surface.

  9. Using Radiochromic Films to Characterize the Dispersion of ZrO{sub 2} Nano-sized Grain Clusters in Protective Polymer Composites

    Energy Technology Data Exchange (ETDEWEB)

    Fontainha, C.C.P.; Nolasco, A.V. [Depto. de Engenharia Nuclear - DEN / UFMG - MG, Av. Antonio Carlos 6627, 31270-970 Belo Horizonte, MG (Brazil); Santos, A.P.; Faria, L.O. [Centro de Desenvolvimento da Tecnologia Nuclear, Av. Antonio Carlos 6627, C.P. 941, 30270-901, Belo Horizonte, MG (Brazil)

    2015-07-01

    . This result is discussed in terms of the high Z halides added to the sensitive layer of EB3 film, once the main components are C (42.3%), H (39.7%) and O (16.0%)1-2. Based on the above results, we have speculated about the abilities of XR-AQ films in the detection of the distribution of nano-sized particles that has high mass-energy attenuation coefficients for low energy x-rays, in polymer composites. In another investigation we tested the ability of XR-QA2 Gafchromic{sup R} films to evaluate the dispersion of ZrO{sub 2} nano-sized grain clusters in protective composites. The P(VDFTrFE)/ ZrO{sub 2} film was sandwiched between two XR-QA2 radiochromic films. In this setup, one radiochromic film is directly exposed to 100 mGy of the x-rays beam and another one measures the attenuated beam. After storage for 24 hours at room temperature under no light conditions, the irradiated radiochromic films were scanned under the same conditions in order to obtain a more reliable result. All films were scanned using the same size ROI in high resolution mode and saved as tagged image file format (TIFF). The untreated scanned image of the XR-AQ2 film directed exposed to the X-ray beam and the correspondent treated image with digital filters are shown. The untreated and treated image of the XR-AQ2 film that was exposed to the attenuated x-ray beam is shown. The image treated with digital filters seems to reproduce the dispersion of ZrO{sub 2} nano-sized grain clusters in the P(VDF-TrFE) copolymer matrix. This result is also discussed in terms of the high Z halides added to the sensitive layer of XR-AQ2 film and compared to the MEV images obtained from the P(VDF-TrFE)/ZrO{sub 2} composites. The results indicate a clear correlation between the 2D radiochromic image and the MEV photography.

  10. Synthesis of 2-Substituted Benzofurans from o-Iodophenols and Terminal Alkynes with a Recyclable Palladium Catalyst Supported on Nano-sized Carbon Balls under Copper- and Ligand-Free Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Yum, Eul Kgun; Yang, Okkyung; Kim, Jieun; Park, Hee Jank [Chungnam National Univ., Daejeon (Korea, Republic of)

    2013-09-15

    We have developed a one-step synthesis of benzofurans from o-iodophenol and various terminal alkynes, by using Pd catalyst supported on nano-sized carbon balls (NCB) under copper- and ligand free conditions. This recyclable catalyst could be reused more than 5 times in the same heteroannulation reaction. The results have demonstrated that diverse 2-substituted benzofurans with tolerant functional groups can be prepared simply and conveniently under these conditions.

  11. Synthesis of 2-Substituted Benzofurans from o-Iodophenols and Terminal Alkynes with a Recyclable Palladium Catalyst Supported on Nano-sized Carbon Balls under Copper- and Ligand-Free Conditions

    International Nuclear Information System (INIS)

    Yum, Eul Kgun; Yang, Okkyung; Kim, Jieun; Park, Hee Jank

    2013-01-01

    We have developed a one-step synthesis of benzofurans from o-iodophenol and various terminal alkynes, by using Pd catalyst supported on nano-sized carbon balls (NCB) under copper- and ligand free conditions. This recyclable catalyst could be reused more than 5 times in the same heteroannulation reaction. The results have demonstrated that diverse 2-substituted benzofurans with tolerant functional groups can be prepared simply and conveniently under these conditions

  12. Synthesis and characterization of scandia ceria stabilized zirconia powders prepared by polymeric precursor method for integration into anode-supported solid oxide fuel cells

    Science.gov (United States)

    Tu, Hengyong; Liu, Xin; Yu, Qingchun

    2011-03-01

    Scandia ceria stabilized zirconia (10Sc1CeSZ) powders are synthesized by polymeric precursor method for use as the electrolyte of anode-supported solid oxide fuel cell (SOFC). The synthesized powders are characterized in terms of crystalline structure, particle shape and size distribution by X-ray diffraction (XRD), transmission electron microscopy (TEM) and photon correlation spectroscopy (PCS). 10Sc1CeSZ electrolyte films are deposited on green anode substrate by screen-printing method. Effects of 10Sc1CeSZ powder characteristics on sintered films are investigated regarding the integration process for application as the electrolytes in anode-supported SOFCs. It is found that the 10Sc1CeSZ films made from nano-sized powders with average size of 655 nm are very porous with many open pores. In comparison, the 10Sc1CeSZ films made from micron-sized powders with average size of 2.5 μm, which are obtained by calcination of nano-sized powders at higher temperatures, are much denser with a few closed pinholes. The cell performances are 911 mW cm-2 at the current density of 1.25 A cm-2 and 800 °C by application of Ce0.8Gd0.2O2 (CGO) barrier layer and La0.6Sr0.4CoO3 (LSC) cathode.

  13. Comparative studies of microstructural, tribological and corrosion properties of Zn-TiO2 and Zn-TiO2-WO3 nano-composite coatings

    Directory of Open Access Journals (Sweden)

    A.A. Daniyan

    Full Text Available Nano sized composites of Zn-TiO2 and Zn-TiO2-WO3 were produced via electrocodeposition on plain carbon steel. The effect of input current on the microstructure, mechanical strengthening and corrosion properties were compared. The morphological features of the composite coatings were characterized by scanning electron microscope (SEM equipped with energy dispersive spectrometer (EDS; mechanical properties were carried out using a diamond base Dura Scan hardness tester and CERT UMT-2 multi-functional tribological tester. The corrosion properties were investigated by potentiodynamic studies in 3.5% NaCl. The result showed that the coatings exhibited good stability and the particle loading of WO3 greatly enhanced the microstructural properties, hardness behaviour and corrosion resistance of the coatings. Keywords: Zn-TiO2, Zn-TiO2-WO3, Electrocodeposition, Microstructure, Composite, Stability and coatings

  14. Powder technology

    International Nuclear Information System (INIS)

    Agueda, Horacio

    1989-01-01

    Powder technology is experiencing nowadays a great development and has broad application in different fields: nuclear energy, medicine, new energy sources, industrial and home artifacts, etc. Ceramic materials are of daily use as tableware and also in the building industry (bricks, tiles, etc.). However, in machine construction its utilization is not so common. The same happens with metals: powder metallurgy is employed less than traditional metal forming techniques. Both cases deal with powder technology and the forming techniques as far as the final consolidation through sintering processes are very similar. There are many different methods and techniques in the forming stage: cold-pressing, slip casting, injection molding, extrusion molding, isostatic pressing, hot-pressing (which involves also the final consolidation step), etc. This variety allows to obtain almost any desired form no matter how complex it could be. Some applications are very specific as in the case of UO 2 pellets (used as nuclear fuels) but with the same technique and other materials, it is possible to manufacture a great number of different products. This work shows the characteristics and behaviour of two magnetic ceramic materials (ferrites) fabricated in the laboratory of the Applied Research Division of the Bariloche Atomic Center for different purposes. Other materials and products made with the same method are also mentioned. Likewise, densities and shrinkage obtained by different methods of forming (cold-pressing, injection molding, slip casting and extrusion molding) using high-purity alumina (99.5% Al 2 O 3 ). Finally, different applications of such methods are given. (Author) [es

  15. Evaluation of heavy metals in hazardous automobile shredder residue thermal residue and immobilization with novel nano-size calcium dispersed reagent

    International Nuclear Information System (INIS)

    Lee, Chi-Hyeon; Truc, Nguyen Thi Thanh; Lee, Byeong-Kyu; Mitoma, Yoshiharu; Mallampati, Srinivasa Reddy

    2015-01-01

    Graphical abstract: Schematic representation of possible mechanisms determining the heavy metals immobilization efficiencyof ASR dust/thermal residues after treatment with nanometallic Ca/CaO/PO 4 . - Highlights: • Nanometallic Ca/CaO/PO 4 for heavy metals immobilization in ASR residue. • Heavy metals immobilization in dry condition attained about 95–100%. • Remaining heavy metals were lower than the Korean standard regulatory limit. • The amounts of heavy metals detectable on the ASR dust surface decreased. • Nanometallic Ca/CaO/PO 4 has a promising potential for heavy metal remediation. - Abstract: This study was conducted to synthesize and apply a nano-size calcium dispersed reagent as an immobilization material for heavy metal-contaminated automobile shredder residues (ASR) dust/thermal residues in dry condition. Simple mixing with a nanometallic Ca/CaO/PO 4 dispersion mixture immobilized 95–100% of heavy metals in ASR dust/thermal residues (including bottom ash, cavity ash, boiler and bag filter ash). The quantity of heavy metals leached from thermal residues after treatment by nanometallic Ca/CaO/PO 4 was lower than the Korean standard regulatory limit for hazardous waste landfills. The morphology and elemental composition of the nanometallic Ca/CaO-treated ASR residue were characterized by field emission scanning election microscopy combined with electron dispersive spectroscopy (FE-SEM/EDS). The results indicated that the amounts of heavy metals detectable on the ASR thermal residue surface decreased and the Ca/PO 4 mass percent increased. X-ray diffraction (XRD) pattern analysis indicated that the main fraction of enclosed/bound materials on ASR residue included Ca/PO 4 − associated crystalline complexes, and that immobile Ca/PO 4 salts remarkably inhibited the desorption of heavy metals from ASR residues. These results support the potential use of nanometallic Ca/CaO/PO 4 as a simple, suitable and highly efficient material for the gentle

  16. Highly selective solid phase extraction and preconcentration of Azathioprine with nano-sized imprinted polymer based on multivariate optimization and its trace determination in biological and pharmaceutical samples

    Energy Technology Data Exchange (ETDEWEB)

    Davarani, Saied Saeed Hosseiny, E-mail: ss-hosseiny@cc.sbu.ac.ir [Faculty of Chemistry, Shahid Beheshti University, G. C., P.O. Box 19839-4716, Tehran (Iran, Islamic Republic of); Rezayati zad, Zeinab [Faculty of Chemistry, Shahid Beheshti University, G. C., P.O. Box 19839-4716, Tehran (Iran, Islamic Republic of); Taheri, Ali Reza; Rahmatian, Nasrin [Islamic Azad University, Ilam Branch, Ilam (Iran, Islamic Republic of)

    2017-02-01

    In this research, for first time selective separation and determination of Azathioprine is demonstrated using molecularly imprinted polymer as the solid-phase extraction adsorbent, measured by spectrophotometry at λ{sub max} 286 nm. The selective molecularly imprinted polymer was produced using Azathioprine and methacrylic acid as a template molecule and monomer, respectively. A molecularly imprinted solid-phase extraction procedure was performed in column for the analyte from pharmaceutical and serum samples. The synthesized polymers were characterized by infrared spectroscopy (IR), field emission scanning electron microscopy (FESEM). In order to investigate the effect of independent variables on the extraction efficiency, the response surface methodology (RSM) based on Box–Behnken design (BBD) was employed. The analytical parameters such as precision, accuracy and linear working range were also determined in optimal experimental conditions and the proposed method was applied to analysis of Azathioprine. The linear dynamic range and limits of detection were 2.5–0.01 and 0.008 mg L{sup ‐1} respectively. The recoveries for analyte were higher than 95% and relative standard deviation values were found to be in the range of 0.83–4.15%. This method was successfully applied for the determination of Azathioprine in biological and pharmaceutical samples. - Graphical abstract: A new-nano sized imprinted polymer was synthesized and applied as sorbent in SPE in order to selective recognition, preconcentration, and determination of Azathioprine with the response surface methodology based on Box–Behnken design and was successfully investigated for the clean-up of human blood serum and pharmaceutical samples. - Highlights: • The nanosized-imprinted polymer has been synthesized by precipitation polymerization technique. • A molecularly imprinted solid-phase extraction procedure was performed for determination of Azathioprine. • The Azathioprine

  17. Evaluation of heavy metals in hazardous automobile shredder residue thermal residue and immobilization with novel nano-size calcium dispersed reagent

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Chi-Hyeon; Truc, Nguyen Thi Thanh [Department of Civil and Environmental Engineering, University of Ulsan, Daehak-ro 93, Nam-gu, Ulsan 680-749 (Korea, Republic of); Lee, Byeong-Kyu, E-mail: bklee@ulsan.ac.kr [Department of Civil and Environmental Engineering, University of Ulsan, Daehak-ro 93, Nam-gu, Ulsan 680-749 (Korea, Republic of); Mitoma, Yoshiharu [Department of Environmental Sciences, Prefectural University of Hiroshima, 562 Nanatsuka-Cho Shobara City, Hiroshima 727-0023 (Japan); Mallampati, Srinivasa Reddy, E-mail: srireddys@ulsan.ac.kr [Department of Civil and Environmental Engineering, University of Ulsan, Daehak-ro 93, Nam-gu, Ulsan 680-749 (Korea, Republic of)

    2015-10-15

    Graphical abstract: Schematic representation of possible mechanisms determining the heavy metals immobilization efficiencyof ASR dust/thermal residues after treatment with nanometallic Ca/CaO/PO{sub 4}. - Highlights: • Nanometallic Ca/CaO/PO{sub 4} for heavy metals immobilization in ASR residue. • Heavy metals immobilization in dry condition attained about 95–100%. • Remaining heavy metals were lower than the Korean standard regulatory limit. • The amounts of heavy metals detectable on the ASR dust surface decreased. • Nanometallic Ca/CaO/PO{sub 4} has a promising potential for heavy metal remediation. - Abstract: This study was conducted to synthesize and apply a nano-size calcium dispersed reagent as an immobilization material for heavy metal-contaminated automobile shredder residues (ASR) dust/thermal residues in dry condition. Simple mixing with a nanometallic Ca/CaO/PO{sub 4} dispersion mixture immobilized 95–100% of heavy metals in ASR dust/thermal residues (including bottom ash, cavity ash, boiler and bag filter ash). The quantity of heavy metals leached from thermal residues after treatment by nanometallic Ca/CaO/PO{sub 4} was lower than the Korean standard regulatory limit for hazardous waste landfills. The morphology and elemental composition of the nanometallic Ca/CaO-treated ASR residue were characterized by field emission scanning election microscopy combined with electron dispersive spectroscopy (FE-SEM/EDS). The results indicated that the amounts of heavy metals detectable on the ASR thermal residue surface decreased and the Ca/PO{sub 4} mass percent increased. X-ray diffraction (XRD) pattern analysis indicated that the main fraction of enclosed/bound materials on ASR residue included Ca/PO{sub 4}− associated crystalline complexes, and that immobile Ca/PO{sub 4} salts remarkably inhibited the desorption of heavy metals from ASR residues. These results support the potential use of nanometallic Ca/CaO/PO{sub 4} as a simple, suitable and

  18. Straightforward fabrication of black nano silica dusting powder for latent fingerprint imaging

    Science.gov (United States)

    Komalasari, Isna; Krismastuti, Fransiska Sri Herwahyu; Elishian, Christine; Handayani, Eka Mardika; Nugraha, Willy Cahya; Ketrin, Rosi

    2017-11-01

    Imaging of latent fingerprint pattern (aka fingermark) is one of the most important and accurate detection methods in forensic investigation because of the characteristic of individual fingerprint. This detection technique relies on the mechanical adherence of fingerprint powder to the moisture and oily component of the skin left on the surface. The particle size of fingerprint powder is one of the critical parameter to obtain excellent fingerprint image. This study develops a simple, cheap and straightforward method to fabricate Nano size black dusting fingerprint powder based on Nano silica and applies the powder to visualize latent fingerprint. The nanostructured silica was prepared from tetraethoxysilane (TEOS) and then modified with Nano carbon, methylene blue and sodium acetate to color the powder. Finally, as a proof-of-principle, the ability of this black Nano silica dusting powder to image latent fingerprint is successfully demonstrated and the results show that this fingerprint powder provides clearer fingerprint pattern compared to the commercial one highlighting the potential application of the nanostructured silica in forensic science.

  19. Synthesis and characterization of heterobinuclear (La-Zn, Pr-Zn, Nd-Zn, Sm-Zn, Eu-Zn, Gd-Zn, Tb-Zn, Dy-Zn) azine-bridged complexes

    International Nuclear Information System (INIS)

    Singh, Bachcha; Srivastav, A.K.; Singh, P.K.

    1997-01-01

    Zinc(II) complex of 2-acetylpyridine salicyl aldazine (Haps) of the type Zn(aps) 2 (H 2 O) 2 has been synthesised. The reaction of Zn(aps) 2 (H 2 O) 2 with lanthanide chlorides, LnCl 3 (where Ln=La, Pr, Nd, Sm, Eu, Gd, Tb and Dy) yields azine-bridged heterobinuclear complexes of the formulae LnCl 3 Zn(aps) 2 (H 2 O) 2 . These complexes have been characterized by elemental analyses, molecular weight, conductance (solid and solution) and magnetic susceptibility measurements, mass, IR and electronic spectral data. X-ray powder diffraction data indicate the tetragonal unit lattice for Zn(aps) 2 (H 2 O) 2 and PrCl 3 Zn(aps) 2 (H 2 O) 2 . (author)

  20. A facile synthesis of ZnS nanocrystallites by pyrolysis of single

    Indian Academy of Sciences (India)

    )2 and ZnCl2 (cinnamtsczH)2 (cinnamtsczH = cinnamaldehyde thiosemicarbazone) as single source precursors. The prepared ZnS nanocrystallites were characterized by powder X-ray diffraction (XRD), transmission electron microscopy ...

  1. PIXE analysis of powdered milk

    International Nuclear Information System (INIS)

    Hallak, A.B.

    1983-01-01

    An accelerator-based study, using proton-induced x-ray emission (PIXE) was performed on four full-cream and four half-cream brands of powdered milk commonly consumed in Jordan. The elements detected in the samples are S, Cl, K, Ca, Fe, Cu, Zn, Br and Rb. The significance of some of these elements is discussed from the viewpoint of nutrition and also their effect on milk processing and dairy technology. The standard reference milk sample, A-11, which is distributed by IAEA was also examined, and the results for trace elements detected are compared with the values certified by IAEA. (author)

  2. Influence of Starting Powders on Hydroxyapatite Coatings Fabricated by Room Temperature Spraying Method.

    Science.gov (United States)

    Seo, Dong Seok; Lee, Jong Kook; Hwang, Kyu Hong; Hahn, Byung Dong; Yoon, Seog Young

    2015-08-01

    Three types of raw materials were used for the fabrication of hydroxyapatite coatings by using the room temperature spraying method and their influence on the microstructure and in vitro characteristics were investigated. Starting hydroxyapatite powders for coatings on titanium substrate were prepared by a heat treatment at 1100 °C for 2 h of bovine bone, bone ash, and commercial hydroxyapatite powders. The phase compositions and Ca/P ratios of the three hydroxyapatite coatings were similar to those of the raw materials without decomposition or formation of a new phase. All hydroxyapatite coatings showed a honeycomb structure, but their surface microstructures revealed different features in regards to surface morphology and roughness, based on the staring materials. All coatings consisted of nano-sized grains and had dense microstructure. Inferred from in vitro experiments in pure water, all coatings have a good dissolution-resistance and biostability in water.

  3. Effect of Co{sup 2+} and Y{sup 3+} ions insertion on the microstructure development and magnetic properties of Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} powders synthesized using Co-precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Rashad, M.M., E-mail: rashad133@yahoo.com [Central Metallurgical Research and Development Institute (CMRDI), P.O. Box 87, Helwan 11421, Cairo (Egypt); Rayan, D.A.; Turky, A.O. [Central Metallurgical Research and Development Institute (CMRDI), P.O. Box 87, Helwan 11421, Cairo (Egypt); Hessien, M.M. [Central Metallurgical Research and Development Institute (CMRDI), P.O. Box 87, Helwan 11421, Cairo (Egypt); Chemistry Department, Taif University (Saudi Arabia)

    2015-01-15

    Nanocrystalline Ni{sub 0.5}Zn{sub 0.5−x}Co{sub x}Fe{sub 2−z}Y{sub z}O{sub 4} powders (x=0–0.3 and z from 0 to 0.3) have been synthesized via a facile co-precipitation technique. X-ray diffraction (XRD), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM) are utilized in order to study the effect of variation of cobalt and yttrium substitutions and its impact on crystalline size, lattice parameter, X-ray density, microstructure and magnetic properties of the formed powders. X-ray diffraction data indicated that, after doping, all samples consisted of the main spinel phase for the formed precursors precipitated at pH 10 annealed at 1000 {sup o}C for 2 h. The lattice parameter and the unit cell were decreased linearly with increasing Co content whereas they were increased with increasing the Y incorporation. Additionally, the porosity was increased with increasing Co concentration while it was decreased with increasing the Y insertion. The mean ionic radii and hopping and bond lengths was decreased with the value of Co{sup 2+} and they were increased with the value of Y{sup 3+} ion as well as both of Y{sup 3+} and Co{sup 2+} ions. The microstructures of the produced powders were found to be cubic like structure. The addition of Y{sup 3+} ion suppressed the grain size whereas addition of Co{sup 2+} ion enhanced the grain growth availably. An examination of the magnetic properties revealed an increase in saturation magnetization with increasing Co and Y concentrations incorporation up to x=0.3. Meanwhile, the formed powders exhibited superparamagnetic characteristics. A high saturation magnetization (77.0 emu/g) was achieved for Ni{sub 0.5}Zn{sub 0.2}Co{sub 0.3}Fe{sub 2}O{sub 4} sample annealed at 1000 {sup o}C for 2 h. - Highlights: • Ni{sub 0.5}Zn{sub 0.5−x}Co{sub x}Fe{sub 2−z}Y{sub z}O{sub 4} powders were synthesized. • The porosity decreases with Y{sup 3+} and increases with Co{sup 2+}. • The bond lengths decrease with Co{sup 2

  4. N-type nano-silicon powders with ultra-low electrical resistivity as anode materials in lithium ion batteries

    Science.gov (United States)

    Yue, Zhihao; Zhou, Lang; Jin, Chenxin; Xu, Guojun; Liu, Liekai; Tang, Hao; Li, Xiaomin; Sun, Fugen; Huang, Haibin; Yuan, Jiren

    2017-06-01

    N-type silicon wafers with electrical resistivity of 0.001 Ω cm were ball-milled to powders and part of them was further mechanically crushed by sand-milling to smaller particles of nano-size. Both the sand-milled and ball-milled silicon powders were, respectively, mixed with graphite powder (silicon:graphite = 5:95, weight ratio) as anode materials for lithium ion batteries. Electrochemical measurements, including cycle and rate tests, present that anode using sand-milled silicon powder performed much better. The first discharge capacity of sand-milled silicon anode is 549.7 mAh/g and it is still up to 420.4 mAh/g after 100 cycles. Besides, the D50 of sand-milled silicon powder shows ten times smaller in particle size than that of ball-milled silicon powder, and they are 276 nm and 2.6 μm, respectively. In addition, there exist some amorphous silicon components in the sand-milled silicon powder excepting the multi-crystalline silicon, which is very different from the ball-milled silicon powder made up of multi-crystalline silicon only.

  5. Effect of nanocomposite packaging containing ZnO on growth of Bacillus subtilis and Enterobacter aerogenes

    Energy Technology Data Exchange (ETDEWEB)

    Esmailzadeh, Hakimeh [National Nutrition and Food Technology Research Institute, Faculty of Nutrition and Food Technology, Shahid Beheshti University of Medical Sciences, Tehran (Iran, Islamic Republic of); Sangpour, Parvaneh, E-mail: Sangpour@merc.ac.ir [Nanotechnology and Advanced Materials Department, Materials and Energy Research Center, Karaj (Iran, Islamic Republic of); Shahraz, Farzaneh [National Nutrition and Food Technology Research Institute, Faculty of Nutrition and Food Technology, Shahid Beheshti University of Medical Sciences, Tehran (Iran, Islamic Republic of); Hejazi, Jalal [Department of Biochemistry and Nutrition, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan (Iran, Islamic Republic of); Khaksar, Ramin [National Nutrition and Food Technology Research Institute, Faculty of Nutrition and Food Technology, Shahid Beheshti University of Medical Sciences, Tehran (Iran, Islamic Republic of)

    2016-01-01

    Recent advances in nanotechnology have opened new windows in active food packaging. Nano-sized ZnO is an inexpensive material with potential antimicrobial properties. The aim of the present study is to evaluate the antibacterial effect of low density Polyethylene (LDPE) containing ZnO nanoparticles on Bacillus subtilis and Enterobacter aerogenes. ZnO nanoparticles have been synthesized by facil molten salt method and have been characterized by X-ray diffraction (XRD), and scanning electron microscopy (SEM). Nanocomposite films containing 2 and 4 wt.% ZnO nanoparticles were prepared by melt mixing in a twin-screw extruder. The growth of both microorganisms has decreased in the presence of ZnO containing nanocomposites compared with controls. Nanocomposites with 4 wt.% ZnO nanoparticles had stronger antibacterial effect against both bacteria in comparison with the 2 wt.% ZnO containing nanocomposites. B. subtilis as Gram-positive bacteria were more sensitive to ZnO containing nanocomposite films compared with E. aerogenes as Gram-negative bacteria. There were no significant differences between the migration of Zn ions from 2 and 4 wt.% ZnO containing nanocomposites and the released Zn ions were not significantly increased in both groups after 14 days compared with the first. Regarding the considerable antibacterial effects of ZnO nanoparticles, their application in active food packaging can be a suitable solution for extending the shelf life of food. - Highlights: • ZnO containing nanocomposites decreased growth of both B. subtilis and E. aerogenes. • B. subtilis was more sensitive to ZnO containing nanocomposites. • The migration of Zn ions from nanocomposites was negligible.

  6. Foundations of powder metallurgy

    International Nuclear Information System (INIS)

    Libenson, G.A.

    1987-01-01

    Consideration is being given to physicochemical foundations and technology of metal powders, moulding and sintering of bars, made of them or their mixtures with nonmetal powders. Data on he design of basic equipment used in the processes of powder metallurgy and its servicing are presented. General requirements of safety engineering when fabricating metal powders and products of them are mentioned

  7. Fundamentals of powder metallurgy

    International Nuclear Information System (INIS)

    Khan, I.H.; Qureshi, K.A.; Minhas, J.I.

    1988-01-01

    This book is being presented to introduce the fundamentals of technology of powder metallurgy. An attempt has been made to present an overall view of powder metallurgy technology in the first chapter, whereas chapter 2 to 8 deal with the production of metal powders. The basic commercial methods of powder production are briefly described with illustrations. Chapter 9 to 12 describes briefly metal powder characteristics and principles of testing, mixing, blending, conditioning, compaction and sintering. (orig./A.B.)

  8. Characteristics of mechanical alloying of Zn-Al-based alloys

    International Nuclear Information System (INIS)

    Zhu, Y.H.; Hong Kong Polytechnic; Perez Hernandez, A.; Lee, W.B.

    2001-01-01

    Three pure elemental powder mixtures of Zn-22%Al-18%Cu, Zn-5%Al-11%Cu, and Zn-27%Al-3%Cu (in wt.%) were mechanically alloyed by steel-ball milling processing. The mechanical alloying characteristics were investigated using X-ray diffraction, scanning electron microscopy, and transmission electron microscopy techniques. It was explored that mechanical alloying started with the formation of phases from pure elemental powders, and this was followed by mechanical milling-induced phase transformation. During mechanical alloying, phases stable at the higher temperatures formed at the near room temperature of milling. Nano-structure Zn-Al-based alloys were produced by mechanical alloying. (orig.)

  9. PEG软模板水热合成纳米氧化锌粉的研究%STUDY ON HYDROTHERMAL SYNTHESIS OF NANOMETER ZnO POWDERS WITH PEG AS A SOFT-TEMPLATE

    Institute of Scientific and Technical Information of China (English)

    孙健; 李小燕; 王艳香

    2010-01-01

    以PEG为软模板水热合成制备纳米氧化锌粉.研究了[Zn2+]和[OH-]摩尔浓度比、不同分子量PEG对纳米氧化锌形貌的影响.采用XRD和SEM对纳米氧化锌粉进行了表征.结果表明:调整[Zn2+]/[OH-]摩尔浓度比,制备出粒状和长棒状的纳米氧化锌.当[Zn2+]/[OH]摩尔浓度比为2时,得到的氧化锌是长棒状,长约为20μm,直径约为3μm.PEG的加入抑制了氧化锌的极性生长,氧化锌由棒状变为近球形的颗粒,并且随着PEG分子量的增加,所得的纳米氧化锌的粒径越小,当PEG的分子量为10000时,所得球形氧化锌的粒径大小为100nm.

  10. Evaluation of undoped ZnS single crystal materials for x-ray imaging applications

    Science.gov (United States)

    Saleh, Muad; Lynn, Kelvin G.; McCloy, John S.

    2017-05-01

    ZnS-based materials have a long history of use as x-ray luminescent materials. ZnS was one of the first discovered scintillators and is reported to have one of the highest scintillator efficiencies. The use of ZnS for high energy luminescence has been thus far limited to thin powder screens, such as ZnS:Ag which is used for detecting alpha radiation, due to opacity to its scintillation light, primarily due to scattering. ZnS in bulk form (chemical vapor deposited, powder processed, and single crystal) has high transmission and low scattering compared to powder screens. In this paper, the performance of single crystalline ZnS is evaluated for low energy x-ray (PLE) of several undoped ZnS single crystals is compared to their Radioluminescence (RL) spectra. It was found that the ZnS emission wavelength varies on the excitation source energy.

  11. HA/nylon 6,6 porous scaffolds fabricated by salt-leaching/solvent casting technique: effect of nano-sized filler content on scaffold properties

    Directory of Open Access Journals (Sweden)

    Mehrabanian M

    2011-08-01

    Full Text Available Mehran Mehrabanian1, Mojtaba Nasr-Esfahani21Member of Young Researchers Club, Najafabad Branch, Islamic Azad University, Isfahan, Iran; 2Department of Materials Science and Engineering, Najafabad Branch, Islamic Azad University, Isfahan, IranAbstract: Nanohydroxyapatite (n-HA/nylon 6,6 composite scaffolds were produced by means of the salt-leaching/solvent casting technique. NaCl with a distinct range size was used with the aim of optimizing the pore network. Composite powders with different n-HA contents (40%, 60% for scaffold fabrication were synthesized and tested. The composite scaffolds thus obtained were characterized for their microstructure, mechanical stability and strength, and bioactivity. The microstructure of the composite scaffolds possessed a well-developed interconnected porosity with approximate optimal pore size ranging from 200 to 500 µm, ideal for bone regeneration and vascularization. The mechanical properties of the composite scaffolds were evaluated by compressive strength and modulus tests, and the results confirmed their similarity to cortical bone. To characterize bioactivity, the composite scaffolds were immersed in simulated body fluid for different lengths of time and results monitored by scanning electron microscopy and energy dispersive X-ray microanalysis to determine formation of an apatite layer on the scaffold surface.Keywords: scaffold, nanohydroxyapatite, nylon 6,6, salt-leaching/solvent casting, bioactivity

  12. Efficient and thermally stable red luminescence from nano-sized phosphor of Gd{sub 6}MoO{sub 12}:Eu{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Qin, Lin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Wei, Donglei [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Huang, Yanlin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Kim, Sun Il [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Yu, Young Moon [Pukyong National University, LED-Marin Convergence Technology R and BD Center (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of)

    2013-09-15

    A novel red-emitting nano-phosphor of Eu{sup 3+}-doped Gd{sub 6}MoO{sub 12} was successfully synthesized by the Pechini method. The crystalline phase was confirmed by X-ray powder diffraction analysis. The morphology of the nano-phosphor was analyzed by scanning electron microscopy, indicating a good crystallization with particles smaller than 500 nm. The luminescence properties such as photoluminescence spectra and decay curves were investigated. The phosphors can be efficiently excited by near-ultraviolet (near-UV) light and exhibit a bright red luminescence around 613 nm ascribed to the forced electric dipole transition {sup 5}D{sub 0}{yields}{sup 7}F{sub 2} of Eu{sup 3+} ions. The thermal stabilities were investigated from the temperature-dependent luminescence decay curves (lifetimes) and spectra intensities. The luminescence properties in relation to applications in white light-emitting diodes (W-LEDs) such as the absolute luminescence quantum efficiency, excitation wavelength, and color coordinates were discussed. The Gd{sub 6}MoO{sub 12}:Eu{sup 3+} nano-phosphor is a promising red-emitting candidate for the fabrication of W-LEDs with near-UV chips.

  13. Synthesis of nano-sized ceria (CeO2 particles via a cerium hydroxy carbonate precursor and the effect of reaction temperature on particle morphology

    Directory of Open Access Journals (Sweden)

    Majid Farahmandjou

    2015-06-01

    Full Text Available Cerium oxide (CeO2 or ceria has been shown to be an interesting support material for noble metals in catalysts designed for emission control, mainly due to its oxygen storage capacity. Ceria nanoparticles were prepared by precipitation method. The precursor materials used in this research were cerium nitrate hexahydrate (as a basic material, potassium carbonate and potassium hydroxide (as precipitants. The morphological properties were characterized by high resolution transmission electron microscopy (HRTEM, scanning electron microscopy (SEM and X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR and UV-Vis spectrophotometer. XRD results showed face centered cubic CeO2 nanoparticles for annealed nanoparticles at 1000°C. SEM measurement showed that by increasing the calcinations temperature from 200 to 600°C, the crystallite size decreased from 90 to 28 nm. The SEM results showed that the size of the CeO2 nanoparticles decreased with increasing temperature. The particle size of CeO2 was around 25 nm as estimated by XRD technique and direct HRTEM observation. SEM and TEM studies showed that the morphology of the prepared powder was sphere-like with a narrow size distribution. The sharp peaks in FTIR spectrum determined the purity of CeO2 nanoparticles and absorbance peak of UV-Vis spectrum showed the small band gap energy of 3.26 ev.

  14. Aluminum powder metallurgy processing

    Energy Technology Data Exchange (ETDEWEB)

    Flumerfelt, J.F.

    1999-02-12

    The objective of this dissertation is to explore the hypothesis that there is a strong linkage between gas atomization processing conditions, as-atomized aluminum powder characteristics, and the consolidation methodology required to make components from aluminum powder. The hypothesis was tested with pure aluminum powders produced by commercial air atomization, commercial inert gas atomization, and gas atomization reaction synthesis (GARS). A comparison of the GARS aluminum powders with the commercial aluminum powders showed the former to exhibit superior powder characteristics. The powders were compared in terms of size and shape, bulk chemistry, surface oxide chemistry and structure, and oxide film thickness. Minimum explosive concentration measurements assessed the dependence of explosibility hazard on surface area, oxide film thickness, and gas atomization processing conditions. The GARS aluminum powders were exposed to different relative humidity levels, demonstrating the effect of atmospheric conditions on post-atomization processing conditions. The GARS aluminum powders were exposed to different relative humidity levels, demonstrating the effect of atmospheric conditions on post-atomization oxidation of aluminum powder. An Al-Ti-Y GARS alloy exposed in ambient air at different temperatures revealed the effect of reactive alloy elements on post-atomization powder oxidation. The pure aluminum powders were consolidated by two different routes, a conventional consolidation process for fabricating aerospace components with aluminum powder and a proposed alternative. The consolidation procedures were compared by evaluating the consolidated microstructures and the corresponding mechanical properties. A low temperature solid state sintering experiment demonstrated that tap densified GARS aluminum powders can form sintering necks between contacting powder particles, unlike the total resistance to sintering of commercial air atomization aluminum powder.

  15. The influence of powder particle size on properties of Cu-Al2O3 composites

    Directory of Open Access Journals (Sweden)

    Rajković V.

    2009-01-01

    Full Text Available Inert gas atomized prealloyed copper powder containing 2 wt.% Al (average particle size ≈ 30 μm and a mixture consisting of copper (average particle sizes ≈ 15 μm and 30 μm and 4 wt.% of commercial Al2O3 powder particles (average particle size ≈ 0.75 μm were milled separately in a high-energy planetary ball mill up to 20 h in air. Milling was performed in order to strengthen the copper matrix by grain size refinement and Al2O3 particles. Milling in air of prealloyed copper powder promoted formation of finely dispersed nano-sized Al2O3 particles by internal oxidation. On the other side, composite powders with commercial micro-sized Al2O3 particles were obtained by mechanical alloying. Following milling, powders were treated in hydrogen at 400 0C for 1h in order to eliminate copper oxides formed on their surface during milling. Hot-pressing (800 0C for 3 h in argon at pressure of 35 MPa was used for compaction of milled powders. Hot-pressed composite compacts processed from 5 and 20 h milled powders were additionally subjected to high temperature exposure (800°C for 1 and 5h in argon in order to examine their thermal stability. The results were discussed in terms of the effects of different size of starting powders, the grain size refinement and different size of Al2O3 particles on strengthening, thermal stability and electrical conductivity of copper-based composites.

  16. Analysis of natural milk and milk powder samples by NAA

    International Nuclear Information System (INIS)

    Al-Jobori, S. M.; Itawi, R. K.; Saad, A; Shihab, K. M.; Jalil, M.; Farhan, S. S.

    1993-01-01

    As a part of the Iraqi food analysis program (IFAP) the concentration of Na, Mg, P, Cl, K, Ca, Zn, Se, Br, Rb, and I in natural milk collected from different regions of Iraq, and in milk powder samples have been determined by using the NAA techniques. It was found that except for the elements I, Rb, and Br the concentrations of the elements was approximately identical in both the natural milk and milk powder. (author)

  17. Analysis of natural milk and milk powder samples by NAA

    International Nuclear Information System (INIS)

    Al-Jobori, S.M.; Itawi, R.K.; Saad, A.; Shihab, K.M.; Jalil, M.; Farhan, S.S.

    1990-01-01

    As a part of the Iraqi Food Analysis Programme the concentration of Na, Mg, P, Cl, K, Ca, Zn, Se, Br, Rb and I in natural milk collected from different regions of Iraq, and in milk powder samples was determined by NAA technique. It was found that except for the elements I, Rb and Br the concentration of the elements was approximately identical in both natural milk and milk powders. (author) 4 refs.; 3 figs.; 5 tabs

  18. Photovoltaic Properties of Co-doped ZnO Thin Film on Glass Substrate

    International Nuclear Information System (INIS)

    Sabia Aye; Zin Ma Ma; May Nwe Oo; Than Than Win; Yin Maung Maung; Ko Ko Kyaw Soe

    2011-12-01

    Cobalt (Co) 0.4 mol doped zinc oxide (ZnO) fine powder was prepared by solid state mixed oxide route. Phase formation and crystal structure of Co-doped ZnO (CZO) powder were examined by X-ray diffraction (XRD). Scanning Electron Microscopy (SEM) was used to observe the micro structure of Co doped ZnO powder. Energy Dispersive X-ray Fluorescent (EDXRF) technique gave the elemental content of cobalt and zinc. Co-doped ZnO film was formed on glass substrate by spin coating technique. Photovoltaic properties of CZO/glass cell were measured.

  19. Multielemental analysis of IAEA intercomparison standard Hay Powder, V-10 and some edible plant leaves by neutron activation. [Br,Ce,Cl,Cr,Cu,Fe,Ga,Hg,K,La,Mn,Mo,Na,P,Sc,Zn

    Energy Technology Data Exchange (ETDEWEB)

    Samudralwar, D L; Wankhade, H K; Garg, A N

    1987-12-01

    Instrumental neutron activation analysis was employed for the multielement determination of an IAEA intercomparison standard Hay Powder, V-10 and some edible plant leaves consumed in India. The samples were irradiated with thermal neutrons at a flux approx. = 10/sup 12/ n x cm/sup -2/ x s/sup -1/ in a reactor for 5 minutes, 1, 2, 5, 10 and 15 hours and counted by high resolution ..gamma..-ray spectrometry. Nearly 18 elements were determined. Good agreement is observed for most of the elements in several NBS standards and the proposed CRM V-10. Some edible vegetable plant leaves were also analyzed. (author) 32 refs.; 3 tabs.

  20. Spherical rhenium metal powder

    International Nuclear Information System (INIS)

    Leonhardt, T.; Moore, N.; Hamister, M.

    2001-01-01

    The development of a high-density, spherical rhenium powder (SReP) possessing excellent flow characteristics has enabled the use of advanced processing techniques for the manufacture of rhenium components. The techniques that were investigated were vacuum plasma spraying (VPS), direct-hot isostatic pressing (D-HIP), and various other traditional powder metallurgy processing methods of forming rhenium powder into near-net shaped components. The principal disadvantages of standard rhenium metal powder (RMP) for advanced consolidation applications include: poor flow characteristics; high oxygen content; and low and varying packing densities. SReP will lower costs, reduce processing times, and improve yields when manufacturing powder metallurgy rhenium components. The results of the powder characterization of spherical rhenium powder and the consolidation of the SReP are further discussed. (author)

  1. A sample holder for in-house X-ray powder diffraction studies of protein powders

    DEFF Research Database (Denmark)

    Frankær, Christian Grundahl; Harris, Pernille; Ståhl, Kenny

    2011-01-01

    A sample holder for handling samples of protein for in-house X-ray powder diffraction (XRPD) analysis has been made and tested on lysozyme. The use of an integrated pinhole reduced the background, and good signal-to-noise ratios were obtained from only 7 l of sample, corresponding to approximatel...... 2-3 mg of dry protein. The sample holder is further adaptable to X-ray absorption spectroscopy (XAS) measurements. Both XRPD and XAS at the Zn K-edge were tested with hexameric Zn insulin....

  2. Mass synthesis of yttrium oxide nano-powders using radio frequency (RF) plasma

    International Nuclear Information System (INIS)

    Ghorui, S.; Sahasrabudhe, S.N.; Chakravarthy, Y.; Nagaraj, A.; Das, A.K.; Dhamale, G.

    2014-01-01

    Mass synthesis of nano-phase Yttrium Oxide (Y 2 O 3 ) from commercially available coarse grain powder is reported. Nano-sized high purity Y 2 O 3 is an important and critical constituent of ceramics like YAG (Yttrium aluminum garnet: Y 3 Al 5 O 12 ) for laser applications. The system is characterized in terms of its thermal and electrical behavior. Boltzmann plot technique is used to measure axial variation of temperature of the generated plasma. The synthesized particles are characterized in terms of XRD, SEM, TEM and BET analyses for qualification of the developed system. Major features observed are efficient conversion into nanometer-sized highly spherical particles, narrow size distribution, highly crystallite nature and highly pure phases. The particle distribution (from TEM) peaks within 20-30 nm. Average particle sizes determined from different methods like XRD, TEM and BET are very close to each other and point toward particle sizes within 20 to 30 nm

  3. Magnetic properties of M0.3Fe2.7O4 (M = Fe, Zn and Mn) ferrites nanoparticles

    Science.gov (United States)

    Modaresi, Nahid; Afzalzadeh, Reza; Aslibeiki, Bagher; Kameli, Parviz

    2018-06-01

    In the present article a comparative study on the structural and magnetic properties of nano-sized M0.3Fe0.7Fe2O4 (M = Fe, Zn and Mn) ferrites have been reported. The X-ray diffraction (XRD) patterns show that the crystallite size depends on the cation distribution. The Rietveld refinement of XRD patterns using MAUD software determines the distribution of cations and unit cell dimensions. The magnetic measurements show that the maximum and minimum value of saturation magnetization is obtained for Zn and Mn doped samples, respectively. The peak temperature of AC magnetic susceptibility of Zn and Fe doped samples below 300 K shows the superparamagnetic behavior in these samples at room temperature. the AC susceptibility results confirm the presence of strong interactions between the nanoparticles which leads to a superspin glass state in the samples at low temperatures.

  4. Study of non-isothermal crystallization of Eu{sup 3+} doped Zn{sub 2}SiO{sub 4} powders through the application of various macrokinetic models

    Energy Technology Data Exchange (ETDEWEB)

    Janković, Bojan, E-mail: bojanjan@ffh.bg.ac.rs [Faculty of Physical Chemistry, Department of the Dynamics and Structure of Matter, University of Belgrade, Studentski trg 12-16, P.O. Box 137, 11001 Belgrade (Serbia); Marinović-Cincović, Milena; Dramićanin, Miroslav D. [Vinča Institute of Nuclear Sciences, University of Belgrade, Mike Petrovića Alasa 12-14, P.O. Box 552, 11001 Belgrade (Serbia)

    2014-02-25

    Highlights: • Europium (Eu{sup 3+}) doped zinc silicate powders. • Sol–gel method. • Stochastic geometric and semi-empirical models. • The interface controlled growth with an increasing nucleation rate. • The improved Nakamura’s model. -- Abstract: Various macrokinetic models (Avrami, Evans, Tobin, Malkin, Dietz, Nakamura, and modified first-order models) were applied to describe non-isothermal crystallization kinetics of Eu{sup 3+} doped zinc silicate powders prepared via the sol–gel method. Analysis of the experimental data was carried out using a direct-fitting method such that the experimental data were fitted directly to each macrokinetic model using a non-linear multivariable regression computation procedure. Comparison of kinetic parameters obtained from the non-linear computation approach to those obtained from the traditional analytical procedure suggested that applicability and reliability of the direct-fitting method were satisfactory. Judging from the quality of the fit, only Nakamura’s model properly describe the temperature dependence of the relative crystallinity, which resulted in the total rejection of the Tobin model in describing the crystallization. With detailed kinetic examination it was concluded that crystallization mechanism of α-willemite doped samples combusted in a microwave oven (MW) follows interface controlled growth with an increasing nucleation rate, attached with geometric process-rate function obeying the improved (corrected) Nakamura’s model. It was found that the presence of non integer Avrami exponent values may indicate that crystallization occurs by more than one reaction mechanism, including the occurrence of autocatalytic behavior of a given system.

  5. Single and double-layer composite microwave absorbers with hexaferrite BaZn{sub 0.6}Zr{sub 0.3}X{sub 0.3}Fe{sub 10.8}O{sub 19} (X = Ti, Ce, Sn) powders

    Energy Technology Data Exchange (ETDEWEB)

    Afghahi, Seyyed Salman Seyyed [Department of Materials Science and Engineering, Imam Hossein University, Tehran (Iran, Islamic Republic of); Jafarian, Mojtaba, E-mail: m.jafarian@srbiau.ac.ir [Young Researchers and Elites Club, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Atassi, Yomen [Department of Applied Physics, Higher Institute for Applied Sciences and Technology, Damascus (Syrian Arab Republic); Stergiou, Charalampos A. [Lab. of Inorganic Materials, Centre for Research and Technology Hellas, 57001, Thermi (Greece)

    2017-01-15

    In the present study, substituted barium hexaferrites with the composition BaZn{sub 0.6}Zr{sub 0.3} × {sub 0.3}Fe{sub 10.8}O{sub 19} (where X = Ti, Ce, Sn) are prepared with the solid-state reaction method. X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometry (VSM) and network analysis techniques are used to analyze the crystal phases, morphology, static magnetic and microwave absorption properties, respectively. Based on the recorded results, barium hexaferrite is the major phase obtained after milling of the powders for 20 h, followed by calcination at 1000 °C for 5 h. The morphology of the particles of the substituted ferrite samples is plate-like with hexagonal shape. The microwave absorption in the X-band of epoxy composites loaded with the ferrite fillers, either separately, in pairs or all together, has been extensively investigated. Multicomponent composites filled with the new hexaferrites under study are promising candidates for electromagnetic absorbers in the 8–12 GHz range. It is found that single-layer absorbers of 5 mm thickness with 45 wt% of a binary (Sn and Ti-doped hexaferrite) or ternary filler mixture exhibit the maximum bandwidth of 2.7 GHz at the level of −10 dB or maximum losses of 26.4 dB at 10.8 GHz, respectively. - Highlights: • Preparation of substituted hexaferrites via mechanical activation. • We designed a broad band microwave absorber with mixing powders. • We designed single layer absorber with RL{sub min} = −26.4 dB and 1.6 GHz bandwidth. • We designed double layer absorbers, as monoband absorbers at a matching frequency.

  6. Development and optimization of iron- and zinc-containing nanostructured powders for nutritional applications

    Energy Technology Data Exchange (ETDEWEB)

    Hilty, F M; Hurrell, R F; Zimmermann, M B [Human Nutrition Laboratory, Institute of Food Science and Nutrition, ETH Zurich (Switzerland); Teleki, A; Buechel, R; Pratsinis, S E [Particle Technology Laboratory, Department of Mechanical and Process Engineering, ETH Zurich (Switzerland); Krumeich, F, E-mail: michael.zimmermann@ilw.agrl.ethz.c [Electron Microscopy Center (EMEZ), ETH Zurich (Switzerland)

    2009-11-25

    Reducing the size of low-solubility iron (Fe)-containing compounds to nanoscale has the potential to improve their bioavailability. Because Fe and zinc (Zn) deficiencies often coexist in populations, combined Fe/Zn-containing nanostructured compounds may be useful for nutritional applications. Such compounds are developed here and their solubility in dilute acid, a reliable indicator of iron bioavailability in humans, and sensory qualities in sensitive food matrices are investigated. Phosphates and oxides of Fe and atomically mixed Fe/Zn-containing (primarily ZnFe{sub 2}O{sub 4}) nanostructured powders were produced by flame spray pyrolysis (FSP). Chemical composition and surface area were systematically controlled by varying precursor concentration and feed rate during powder synthesis to increase solubility to the level of ferrous sulfate at maximum Fe and Zn content. Solubility of the nanostructured compounds was dependent on their particle size and crystallinity. The new nanostructured powders produced minimal color changes when added to dairy products containing chocolate or fruit compared to the changes produced when ferrous sulfate or ferrous fumarate were added to these foods. Flame-made Fe- and Fe/Zn-containing nanostructured powders have solubilities comparable to ferrous and Zn sulfate but may produce fewer color changes when added to difficult-to-fortify foods. Thus, these powders are promising for food fortification and other nutritional applications.

  7. Development and optimization of iron- and zinc-containing nanostructured powders for nutritional applications

    International Nuclear Information System (INIS)

    Hilty, F M; Hurrell, R F; Zimmermann, M B; Teleki, A; Buechel, R; Pratsinis, S E; Krumeich, F

    2009-01-01

    Reducing the size of low-solubility iron (Fe)-containing compounds to nanoscale has the potential to improve their bioavailability. Because Fe and zinc (Zn) deficiencies often coexist in populations, combined Fe/Zn-containing nanostructured compounds may be useful for nutritional applications. Such compounds are developed here and their solubility in dilute acid, a reliable indicator of iron bioavailability in humans, and sensory qualities in sensitive food matrices are investigated. Phosphates and oxides of Fe and atomically mixed Fe/Zn-containing (primarily ZnFe 2 O 4 ) nanostructured powders were produced by flame spray pyrolysis (FSP). Chemical composition and surface area were systematically controlled by varying precursor concentration and feed rate during powder synthesis to increase solubility to the level of ferrous sulfate at maximum Fe and Zn content. Solubility of the nanostructured compounds was dependent on their particle size and crystallinity. The new nanostructured powders produced minimal color changes when added to dairy products containing chocolate or fruit compared to the changes produced when ferrous sulfate or ferrous fumarate were added to these foods. Flame-made Fe- and Fe/Zn-containing nanostructured powders have solubilities comparable to ferrous and Zn sulfate but may produce fewer color changes when added to difficult-to-fortify foods. Thus, these powders are promising for food fortification and other nutritional applications.

  8. Development and optimization of iron- and zinc-containing nanostructured powders for nutritional applications.

    Science.gov (United States)

    Hilty, F M; Teleki, A; Krumeich, F; Büchel, R; Hurrell, R F; Pratsinis, S E; Zimmermann, M B

    2009-11-25

    Reducing the size of low-solubility iron (Fe)-containing compounds to nanoscale has the potential to improve their bioavailability. Because Fe and zinc (Zn) deficiencies often coexist in populations, combined Fe/Zn-containing nanostructured compounds may be useful for nutritional applications. Such compounds are developed here and their solubility in dilute acid, a reliable indicator of iron bioavailability in humans, and sensory qualities in sensitive food matrices are investigated. Phosphates and oxides of Fe and atomically mixed Fe/Zn-containing (primarily ZnFe2O4) nanostructured powders were produced by flame spray pyrolysis (FSP). Chemical composition and surface area were systematically controlled by varying precursor concentration and feed rate during powder synthesis to increase solubility to the level of ferrous sulfate at maximum Fe and Zn content. Solubility of the nanostructured compounds was dependent on their particle size and crystallinity. The new nanostructured powders produced minimal color changes when added to dairy products containing chocolate or fruit compared to the changes produced when ferrous sulfate or ferrous fumarate were added to these foods. Flame-made Fe- and Fe/Zn-containing nanostructured powders have solubilities comparable to ferrous and Zn sulfate but may produce fewer color changes when added to difficult-to-fortify foods. Thus, these powders are promising for food fortification and other nutritional applications.

  9. Near band edge emission characteristics of sputtered nano-crystalline ZnO films

    International Nuclear Information System (INIS)

    Kunj, Saurabh; Sreenivas, K.

    2016-01-01

    Sputtered zinc oxide (ZnO) thin films deposited on unheated glass substrate under different sputtering gas mixtures (Ar+O_2) have been investigated using X-ray diffraction and photo luminescence spectroscopy. Earlier reported studies on ZnO films prepared by different techniques exhibit either a sharp/broad near band edge (NBE) emission peak depending on the crystalline quality of the film. In the present study zinc oxide films, grown on unheated substrates, are seen to possess a preferred (002) orientation with a microstructure consisting of clustered nano-sized crystallites. The splitting in the near band edge emission (NBE) into three characteristic peaks is attributed to quantum confinement effect, and is observed specifically under an excitation of 270 nm. Deep level emission (DLE) in the range 400 to 700 nm is not observed indicating absence of deep level radiative defects.

  10. Near band edge emission characteristics of sputtered nano-crystalline ZnO films

    Science.gov (United States)

    Kunj, Saurabh; Sreenivas, K.

    2016-05-01

    Sputtered zinc oxide (ZnO) thin films deposited on unheated glass substrate under different sputtering gas mixtures (Ar+O2) have been investigated using X-ray diffraction and photo luminescence spectroscopy. Earlier reported studies on ZnO films prepared by different techniques exhibit either a sharp/broad near band edge (NBE) emission peak depending on the crystalline quality of the film. In the present study zinc oxide films, grown on unheated substrates, are seen to possess a preferred (002) orientation with a microstructure consisting of clustered nano-sized crystallites. The splitting in the near band edge emission (NBE) into three characteristic peaks is attributed to quantum confinement effect, and is observed specifically under an excitation of 270 nm. Deep level emission (DLE) in the range 400 to 700 nm is not observed indicating absence of deep level radiative defects.

  11. Near band edge emission characteristics of sputtered nano-crystalline ZnO films

    Energy Technology Data Exchange (ETDEWEB)

    Kunj, Saurabh; Sreenivas, K. [Department of Physics & Astrophysics, University of Delhi, Delhi 110007 INDIA (India)

    2016-05-06

    Sputtered zinc oxide (ZnO) thin films deposited on unheated glass substrate under different sputtering gas mixtures (Ar+O{sub 2}) have been investigated using X-ray diffraction and photo luminescence spectroscopy. Earlier reported studies on ZnO films prepared by different techniques exhibit either a sharp/broad near band edge (NBE) emission peak depending on the crystalline quality of the film. In the present study zinc oxide films, grown on unheated substrates, are seen to possess a preferred (002) orientation with a microstructure consisting of clustered nano-sized crystallites. The splitting in the near band edge emission (NBE) into three characteristic peaks is attributed to quantum confinement effect, and is observed specifically under an excitation of 270 nm. Deep level emission (DLE) in the range 400 to 700 nm is not observed indicating absence of deep level radiative defects.

  12. SAF line powder operations

    International Nuclear Information System (INIS)

    Frederickson, J.R.; Horgos, R.M.

    1983-10-01

    An automated nuclear fuel fabrication line is being designed for installation in the Fuels and Materials Examination Facility (FMEF) near Richland, Washington. The fabrication line will consist of seven major process systems: Receiving and Powder Preparation; Powder Conditioning; Pressing and Boat Loading; Debinding, Sintering, and Property Adjustment; Boat Transport; Pellet Inspection and Finishing; and Pin Operations. Fuel powder processing through pellet pressing will be discussed in this paper

  13. Two layer powder pressing

    International Nuclear Information System (INIS)

    Schreiner, H.

    1979-01-01

    First, significance and advantages of sintered materials consisting of two layers are pointed out. By means of the two layer powder pressing technique metal powders are formed resulting in compacts with high accuracy of shape and mass. Attributes of basic powders, different filling methods and pressing techniques are discussed. The described technique is supposed to find further applications in the field of two layer compacts in the near future

  14. Operation whey powder

    International Nuclear Information System (INIS)

    Brunner, E.

    1987-01-01

    The odyssey of the contaminated whey powder finally has come to an end, and the 5000 tonnes of whey now are designated for decontamination by means of an ion exchange technique. The article throws light upon the political and economic reasons that sent the whey powder off on a chaotic journey. It is worth mentioning in this context that the natural radioactivity of inorganic fertilizers is much higher than that of the whey powder in question. (HP) [de

  15. Pharmaceutical powder compaction technology

    National Research Council Canada - National Science Library

    Çelik, Metin

    2011-01-01

    ... through the compaction formulation process and application. Compaction of powder constituents both active ingredient and excipients is examined to ensure consistent and reproducible disintegration and dispersion profiles...

  16. Positron annihilation study of mechanochemical reaction between Zn+Se and Zn+S

    International Nuclear Information System (INIS)

    Kajcsos, Zs.; Horvath, D.; Tshakarov, C.G.; Gospodinov, G.G.; Vertes, A.

    1981-01-01

    Positron lifetime spectra were recorded and evaluated in mixtures of Zn+S and Zn+Se powders for various periods. The intensity of the long-lived positron lifetime component is shown to increase with grinding time until an abrupt decrease takes place at a specific grinding time, indicating the onset of the effective chemical reaction. The suitability of positron annihilation for investigating mechanochemical reactions is clearly demonstrated. (author)

  17. Biaxially textured articles formed by powder metallurgy

    Science.gov (United States)

    Goyal, Amit; Williams, Robert K.; Kroeger, Donald M.

    2003-08-05

    A biaxially textured alloy article having a magnetism less than pure Ni includes a rolled and annealed compacted and sintered powder-metallurgy preform article, the preform article having been formed from a powder mixture selected from the group of ternary mixtures consisting of: Ni powder, Cu powder, and Al powder, Ni powder, Cr powder, and Al powder; Ni powder, W powder and Al powder; Ni powder, V powder, and Al powder; Ni powder, Mo powder, and Al powder; the article having a fine and homogeneous grain structure; and having a dominant cube oriented {100} orientation texture; and further having a Curie temperature less than that of pure Ni.

  18. Simple Preparation of ZnO Nano-layer by Sol-Gel Method as Active Electrode in P3HT/ZnO Heterojunction Solar Cell

    Science.gov (United States)

    Aprilia, Annisa; Herman, Hidayat, Rahmat

    2010-10-01

    Highly transparent undoped ZnO thin films have been prepared on glass and indium tin oxide substrates with simple process by sol-gel route and dip-coating deposition. Gel precursor of ZnO was prepared from zinc acetat dehydrate solution in methanol with the addition of trietylamine as stabilizing agent. Thin layer of gel precursor was prepared by dip coating and then followed by calcination at 400° C for 5 minute in air atmosphere. The thickness of the resulted ZnO thin film produced by ten times coating is about 150 nm. The films shows high transmittance larger than 98% in the visible region (400-800 nm). Absorption is observed in the UV region with absorption onset at about 390 nm indicating varying band gap between 3.18 eV until 3.23 eV depending on the number of coating layer. The AFM image shows that the films seems to be constructed from random stacking of nano-sized ZnO particle in the order of 50 nm. Among the prepared samples, the lowest resistivity is about 1.8×107 Ωm observed in the five-layer coating film. In order to fabricate solar cell structure, P3HT was deposited onto the ZnO thin film layer by spin casting technique and then followed by metal (Au) layer deposition by thermal evaporation. The formed solar cell has the inverted type solar cell with ITO/ZnO/P3HT/Au configuration. By the insertion ZnO layer, the photocurrent was improved by more than ten orders of magnitude in comparison to that of without ZnO layer. The measured photocurrent decreases at large number of coating layer which is supposed to be related with the current limitation by the effective carrier path length in ZnO layer.

  19. Sintered aluminium powders

    International Nuclear Information System (INIS)

    Stepanova, M.G.; Matveev, B.I.

    1974-01-01

    The mechanical and physical properties of aluminium powder alloys and the various methods employed to produce them are considered. Data are given on the hardening of the alloys SAP and SPAK-4, as well as the powder-alloy system Al-Cr-Zr. (L.M.)

  20. Phase transformation from cubic ZnS to hexagonal ZnO by thermal annealing

    Science.gov (United States)

    Mahmood, K.; Asghar, M.; Amin, N.; Ali, Adnan

    2015-03-01

    We have investigated the mechanism of phase transformation from ZnS to hexagonal ZnO by high-temperature thermal annealing. The ZnS thin films were grown on Si (001) substrate by thermal evaporation system using ZnS powder as source material. The grown films were annealed at different temperatures and characterized by X-ray diffraction (XRD), photoluminescence (PL), four-point probe, scanning electron microscope (SEM) and energy dispersive X-ray diffraction (EDX). The results demonstrated that as-deposited ZnS film has mixed phases but high-temperature annealing leads to transition from ZnS to ZnO. The observed result can be explained as a two-step process: (1) high-energy O atoms replaced S atoms in lattice during annealing process, and (2) S atoms diffused into substrate and/or diffused out of the sample. The dissociation energy of ZnS calculated from the Arrhenius plot of 1000/T versus log (resistivity) was found to be 3.1 eV. PL spectra of as-grown sample exhibits a characteristic green emission at 2.4 eV of ZnS but annealed samples consist of band-to-band and defect emission of ZnO at 3.29 eV and 2.5 eV respectively. SEM and EDX measurements were additionally performed to strengthen the argument.

  1. Optically stimulated luminescence of ZnO obtained by thermal treatment of ZnS chemically synthesized; Luminiscencia opticamente estimulada de ZnO obtenido por tratamiento termico de ZnS sintetizado quimicamente

    Energy Technology Data Exchange (ETDEWEB)

    Cruz V, C.; Burruel I, S.E.; Orante B, V.R.; Grijalva M, H.; Perez S, R.; Bernal, R. [Universidad de Sonora, A.P. 130, Hermosillo (Mexico)

    2005-07-01

    In this work, we report the optically stimulated luminescence (OSL) dosimetry of new nano phosphors of ZnO obtained by thermal annealing of chemically synthesized ZnS powder. The synthesized ZnS nano powder was compressed in order to form pellet shaped pellets, which were afterwards subjected to a thermal annealing at 700 C during 24 h under air atmosphere. X-ray diffraction (XRD) patterns and energy-disperse X-ray Spectrometry (EDS) analyses confirmed the transformation of ZnS to ZnO. Samples were exposed to several doses of beta radiation up to 600 Gy, and the optically stimulated luminescence with 470 nm wavelength light was recorded as a function of dose. The intensity of the OSL signal increases by increasing dose, for what it is concluded that these new phosphor materials are suitable to be used in optically stimulated luminescence dosimetry. (Author)

  2. The synthesis and photocatalytic activity of ZnSe microspheres

    International Nuclear Information System (INIS)

    Cao Huaqiang; Xiao Yujiang; Zhang Sichun

    2011-01-01

    This paper reports the synthesis of semiconductor ZnSe microspheres composed of nanoparticles via a solvothermal route between the organic molecule selenophene (C 4 H 4 Se) and ZnCl 2 without adding any surfactant. The ZnSe microspheres were characterized by x-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), specific surface area measurement, and photoluminescence (PL) spectra. A strong and broad blue PL emission at 443 nm in wavelength (∼2.79 eV in photon energy) is attributed to the near-band-edge (NBE) emission of ZnSe, while the 530 nm peak is a defect-related (DL) emission. The photocatalytic activity of the as-prepared ZnSe microspheres was evaluated by photodegradation of methyl orange (MO) dye under ultraviolet (UV) light and visible light irradiation. The degradations of MO reach 94% or 95.1%, close to 100%, in the presence of the as-synthesized ZnSe microspheres or commercial ZnSe powder after 7 or 10 h under UV irradiation, respectively. Meanwhile the degradations of MO reach 94.3% or 60.6% in the presence of the as-synthesized ZnSe microspheres or commercial ZnSe powder after 12 h, respectively. The degradation rate of ZnSe microspheres is twice that of ZnSe commercial powder under UV light irradiation, and three times under visible light irradiation. The degradation process of MO dye on ZnSe microspheres under UV or visible light is also discussed.

  3. Measurement of loose powder density

    International Nuclear Information System (INIS)

    Akhtar, S.; Ali, A.; Haider, A.; Farooque, M.

    2011-01-01

    Powder metallurgy is a conventional technique for making engineering articles from powders. Main objective is to produce final products with the highest possible uniform density, which depends on the initial loose powder characteristics. Producing, handling, characterizing and compacting materials in loose powder form are part of the manufacturing processes. Density of loose metallic or ceramic powder is an important parameter for die design. Loose powder density is required for calculating the exact mass of powder to fill the die cavity for producing intended green density of the powder compact. To fulfill this requirement of powder metallurgical processing, a loose powder density meter as per ASTM standards is designed and fabricated for measurement of density. The density of free flowing metallic powders can be determined using Hall flow meter funnel and density cup of 25 cm/sup 3/ volume. Density of metal powders like cobalt, manganese, spherical bronze and pure iron is measured and results are obtained with 99.9% accuracy. (author)

  4. Optically stimulated luminescence of ZnO obtained by thermal treatment of ZnS chemically synthesized

    International Nuclear Information System (INIS)

    Cruz V, C.; Burruel I, S.E.; Orante B, V.R.; Grijalva M, H.; Perez S, R.; Bernal, R.

    2005-01-01

    In this work, we report the optically stimulated luminescence (OSL) dosimetry of new nano phosphors of ZnO obtained by thermal annealing of chemically synthesized ZnS powder. The synthesized ZnS nano powder was compressed in order to form pellet shaped pellets, which were afterwards subjected to a thermal annealing at 700 C during 24 h under air atmosphere. X-ray diffraction (XRD) patterns and energy-disperse X-ray Spectrometry (EDS) analyses confirmed the transformation of ZnS to ZnO. Samples were exposed to several doses of beta radiation up to 600 Gy, and the optically stimulated luminescence with 470 nm wavelength light was recorded as a function of dose. The intensity of the OSL signal increases by increasing dose, for what it is concluded that these new phosphor materials are suitable to be used in optically stimulated luminescence dosimetry. (Author)

  5. Photoluminescent properties of ZnS nanoparticles prepared by electro-explosion of Zn wires

    International Nuclear Information System (INIS)

    Goswami, Navendu; Sen, P.

    2007-01-01

    We study the photoluminescent properties of ZnS nanoparticles without the influence of dopants or magnetic impurities. The ZnS nanoparticles reported in this case were synthesized by a novel method of electro-explosion of wire (EEW). The nanoparticles were prepared employing electro-explosion of pure zinc wires in a cell filled with sulfide ions to produce a free-standing compound ZnS semiconductor. To investigate the structural and optical properties, these nanoparticles were characterized by X-ray powder diffraction (XRD), atomic force microscopy (AFM), UV-visible and photoluminescence (PL) spectroscopy. Consistent with the enhancement of the PL intensity of the 443 nm peak due to deep blue emission of ZnS particles, the XRD of the nanoparticles reveals a hexagonal phase of ZnS nanocrystallites prepared by our novel synthesis technique

  6. Size-dependent magnetic and structural properties of CoCrFeO4 nano-powder prepared by solution self-combustion

    Science.gov (United States)

    Sijo, A. K.; Dutta, Dimple P.

    2018-04-01

    The study reports the tuning of magnetic and structural properties of nano-sized CoCrFeO4 via post-annealing treatment. CoCrFeO4 nano-powder has been prepared by solution self-combustion method. The structural and magnetic properties have been studied over a range of annealing temperatures (300-900 °C). The formation of the phase pure CoCrFeO4 spinel has been confirmed from powder XRD analysis. The crystallite size is observed to increase with an increase in annealing temperature. On annealing, the value of magnetic parameters-remanence, coercivity and saturation magnetization have enhanced. All the samples exhibit irreversibility at low-temperature measurements.

  7. Preparation and electrochemical characterization of size controlled SnO2-RuO2 composite powder for monolithic hybrid battery

    International Nuclear Information System (INIS)

    Jeon, Young-Ah; No, Kwang-Soo; Choi, Sun Hee; Ahn, Jae pyong; Yoon, Young Soo

    2004-01-01

    Tin oxide (SnO 2 ) powders with a particle size of ∼20 nm were synthesized by a gas condensation method. Ruthenium oxide was loaded by an incipient-wetness method, in which an aqueous solution of RuCl 3 was added to the manufactured SnO 2 powder in an amount that was just sufficient to wet completely the powder. And then, the resulting solution was obtained after freeze-drying to synthesis the smallest particle. The as-synthesized SnO 2 powder with 1.5 wt.% ruthenium oxide (RuO 2 ) exhibited well-developed facets and had a very uniform particle size. The first discharge capacity was lower than comparing to commercial powder because of forming the second phase, but showed good cyclability. A maximum specific electrode capacitance of ∼20 F/g and a maximum specific power of ∼80 W/kg were achieved by manufactured SnO 2 with 1.5 wt.% RuO 2 . This result indicated that the synthesized SnO 2 -RuO 2 composite powder of nano-size scale is candidate for use in fabricating monolithic hybrid batteries using suitable electrolyte as well

  8. The influence of Span-20 surfactant and micro-/nano-Chromium (Cr) Powder Mixed Electrical Discharge Machining (PMEDM) on the surface characteristics of AISI D2 hardened steel

    Science.gov (United States)

    Hosni, N. A. J.; Lajis, M. A.

    2018-04-01

    The application of powder mixed dielectric to improve the efficiency of electrical discharge machining (EDM) has been extensively studied. Therefore, PMEDM have attracted the attention of many researchers since last few decades. Improvement in EDM process has resulted in the use of span-20 surfactant and Cr powder mixed in dielectric fluid, which results in increasing machiniability, better surface quality and faster machining time. However, the study of powder suspension size of surface charateristics in EDM field is still limited. This paper presents the improvement of micro-/nano- Cr powder size on the surface characteristics of the AISI D2 hardened steels in PMEDM. It has found that the reacst layer in PMEDM improved by as high as 41-53 % compared to conventional EDM. Also notably, the combination of added Cr powder and span-20 surfactant reduced the recast layer thickness significantly especially in nano-Cr size. This improvement was great potential adding nano-size Cr powder to dielectric for machining performance.

  9. Structural stability of nano-sized clusters

    NARCIS (Netherlands)

    De Hosson, JTM; Palasantzas, G; Vystavel, T; Koch, S; Ovidko,; Pande, CS; Krishnamoorti, R; Lavernia, E; Skandan, G

    2004-01-01

    This contribution presents challenges to control the microstructure in nano-structured materials via a relatively new approach, i.e. using a so-called nanocluster source. An important aspect is that the cluster size distribution is monodisperse and that the kinetic energy of the clusters during

  10. Olefin metathesis in nano-sized systems

    Directory of Open Access Journals (Sweden)

    Denise Méry

    2011-01-01

    Full Text Available The interplay between olefin metathesis and dendrimers and other nano systems is addressed in this mini review mostly based on the authors’ own contributions over the last decade. Two subjects are presented and discussed: (i The catalysis of olefin metathesis by dendritic nano-catalysts via either covalent attachment (ROMP or, more usefully, dendrimer encapsulation – ring closing metathesis (RCM, cross metathesis (CM, enyne metathesis reactions (EYM – for reactions in water without a co-solvent and (ii construction and functionalization of dendrimers by CM reactions.

  11. Synthesis of Cu-coated Graphite Powders Using a Chemical Reaction Process

    Energy Technology Data Exchange (ETDEWEB)

    Jang, Jun-Ho; Park, Hyun-Kuk; Oh, Ik-Hyun [Korea Institute of Industrial Technology (KITECH), Gwangju (Korea, Republic of); Lim, Jae-Won [Chonbuk National University, Jeonju (Korea, Republic of)

    2017-05-15

    In this paper, Cu-coated graphite powders for a low thermal expansion coefficient and a high thermal conductivity are fabricated using a chemical reaction process. The Cu particles adhere to the irregular graphite powders and they homogeneously disperse in the graphite matrix. Cu-coated graphite powders are coarser at approximately 3-4 μm than the initial graphite powders; furthermore, their XRD patterns exhibit a low intensity in the oxide peak with low Zn powder content. For the passivation powders, the transposition solvent content has low values, and the XRD pattern of the oxide peaks is almost non-existent, but the high transposition solvent content does not exhibit a difference to the non-passivation treated powders.

  12. POWDER COAT APPLICATIONS

    Science.gov (United States)

    The report discusses an investigation of critical factors that affect the use of powder coatings on the environment, cost, quality, and production. The investigation involved a small business representative working with the National Defense Center for Environmental Excellence (ND...

  13. OIL SOLUTIONS POWDER

    Science.gov (United States)

    Technical product bulletin: aka OIL SOLUTIONS POWDER, SPILL GREEN LS, this miscellaneous oil spill control agent used in cleanups initially behaves like a synthetic sorbent, then as a solidifier as the molecular microencapsulating process occurs.

  14. Green method for producing hierarchically assembled pristine porous ZnO nanoparticles with narrow particle size distribution

    International Nuclear Information System (INIS)

    Escobedo-Morales, A.; Téllez-Flores, D.; Ruiz Peralta, Ma. de Lourdes; Garcia-Serrano, J.; Herrera-González, Ana M.; Rubio-Rosas, E.; Sánchez-Mora, E.; Olivares Xometl, O.

    2015-01-01

    A green method for producing pristine porous ZnO nanoparticles with narrow particle size distribution is reported. This method consists in synthesizing ZnO 2 nanopowders via a hydrothermal route using cheap and non-toxic reagents, and its subsequent thermal decomposition at low temperature under a non-protective atmosphere (air). The morphology, structural and optical properties of the obtained porous ZnO nanoparticles were studied by means of powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and nitrogen adsorption–desorption measurements. It was found that after thermal decomposition of the ZnO 2 powders, pristine ZnO nanoparticles are obtained. These particles are round-shaped with narrow size distribution. A further analysis of the obtained ZnO nanoparticles reveals that they are hierarchical self-assemblies of primary ZnO particles. The agglomeration of these primary particles at the very early stage of the thermal decomposition of ZnO 2 powders provides to the resulting ZnO nanoparticles a porous nature. The possibility of using the synthesized porous ZnO nanoparticles as photocatalysts has been evaluated on the degradation of rhodamine B dye. - Highlights: • A green synthesis method for obtaining porous ZnO nanoparticles is reported. • The obtained ZnO nanoparticles have narrow particle size distribution. • This method allows obtaining pristine ZnO nanoparticles avoiding unintentional doping. • A growth mechanism for the obtained porous ZnO nanoparticles is proposed

  15. Synthesis of nano-sized stereoselective imprinted polymer by copolymerization of (S)-2-(acrylamido) propanoic acid and ethylene glycol dimethacrylate in the presence of racemic propranolol and copper ion

    Energy Technology Data Exchange (ETDEWEB)

    Alizadeh, Taher, E-mail: talizadeh@ut.ac.ir [Department of Analytical Chemistry, Faculty of Chemistry, University College of Science, University of Tehran, P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of); Bagherzadeh, Azam; Shamkhali, Amir Nasser [Department of Applied Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of)

    2016-06-01

    A new chiral functional monomer of (S)-2-(acrylamido) propanoic acid was obtained by reaction of (L)-alanine with acryloyl chloride. The resulting monomer was characterized by FT-IR and HNMR and then utilized for the preparation of chiral imprinted polymer (CIP). This was carried out by copolymerization of (L)-alanine-derived chiral monomer and ethylene glycol dimethacrylate, in the presence of racemic propranolol and copper nitrate, via precipitation polymerization technique, resulting in nano-sized networked polymer particles. The polymer obtained was characterized by scanning electron microscopy and FT-IR. The non-imprinted polymer was also synthesized and used as blank polymer. Density functional theory (DFT) was also employed to optimize the structures of two diasterometric ternary complexes, suspected to be created in the pre-polymerization step, by reaction of optically active isomers of propranolol, copper ion and (S)-2-(acrylamido) propanoic acid. Relative energies and other characteristics of the described complexes, calculated by the DFT, predicted the higher stability of (S)-propranolol involved complex, compared to (R)-propranolol participated complex. Practical batch extraction test which employed CIP as solid phase adsorbent, indicated that the CIP recognized selectively (S)-propranolol in the racemic mixture of propranolol; whereas, the non-imprinted polymer (NIP) showed no differentiation capability between two optically active isomers of propranolol. - Highlights: • A new chiral functional monomer of (S)-2-(acrylamido) propanoic acid was synthesized. • (S)-propranolol-selective imprinted polymer was synthesized using the chiral monomer. • Racemic propranolol mixed with Cu(II) was used as template in the imprinting. • Density functional theory was employed to clarify the imprinting mechanism. • (S)-propranolol-Cu(II) complex was shown to conduct the imprinting process.

  16. Magnetically responsive enzyme powders

    Energy Technology Data Exchange (ETDEWEB)

    Pospiskova, Kristyna, E-mail: kristyna.pospiskova@upol.cz [Regional Centre of Advanced Technologies and Materials, Palacky University, Slechtitelu 11, 783 71 Olomouc (Czech Republic); Safarik, Ivo, E-mail: ivosaf@yahoo.com [Regional Centre of Advanced Technologies and Materials, Palacky University, Slechtitelu 11, 783 71 Olomouc (Czech Republic); Department of Nanobiotechnology, Institute of Nanobiology and Structural Biology of GCRC, Na Sadkach 7, 370 05 Ceske Budejovice (Czech Republic)

    2015-04-15

    Powdered enzymes were transformed into their insoluble magnetic derivatives retaining their catalytic activity. Enzyme powders (e.g., trypsin and lipase) were suspended in various liquid media not allowing their solubilization (e.g., saturated ammonium sulfate and highly concentrated polyethylene glycol solutions, ethanol, methanol, 2-propanol) and subsequently cross-linked with glutaraldehyde. Magnetic modification was successfully performed at low temperature in a freezer (−20 °C) using magnetic iron oxides nano- and microparticles prepared by microwave-assisted synthesis from ferrous sulfate. Magnetized cross-linked enzyme powders were stable at least for two months in water suspension without leakage of fixed magnetic particles. Operational stability of magnetically responsive enzymes during eight repeated reaction cycles was generally without loss of enzyme activity. Separation of magnetically modified cross-linked powdered enzymes from reaction mixtures was significantly simplified due to their magnetic properties. - Highlights: • Cross-linked enzyme powders were prepared in various liquid media. • Insoluble enzymes were magnetized using iron oxides particles. • Magnetic iron oxides particles were prepared by microwave-assisted synthesis. • Magnetic modification was performed under low (freezing) temperature. • Cross-linked powdered trypsin and lipase can be used repeatedly for reaction.

  17. Characteristics of Inconel Powders for Powder-Bed Additive Manufacturing

    Directory of Open Access Journals (Sweden)

    Quy Bau Nguyen

    2017-10-01

    Full Text Available In this study, the flow characteristics and behaviors of virgin and recycled Inconel powder for powder-bed additive manufacturing (AM were studied using different powder characterization techniques. The results revealed that the particle size distribution (PSD for the selective laser melting (SLM process is typically in the range from 15 μm to 63 μm. The flow rate of virgin Inconel powder is around 28 s·(50 g−1. In addition, the packing density was found to be 60%. The rheological test results indicate that the virgin powder has reasonably good flowability compared with the recycled powder. The inter-relation between the powder characteristics is discussed herein. A propeller was successfully printed using the powder. The results suggest that Inconel powder is suitable for AM and can be a good reference for researchers who attempt to produce AM powders.

  18. Effect of shallow donors on Curie–Weiss temperature of Co-doped ZnO

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Shuxia, E-mail: gsx0391@sina.com [Department of Physics, Jiaozuo Teachers College, Jiaozuo 454001 (China); Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China); Li, Jiwu [Department of Physics, Jiaozuo Teachers College, Jiaozuo 454001 (China); Du, Zuliang [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China)

    2014-12-15

    Co-doped ZnO and Al, Co co-doped ZnO polycrystalline powders were synthesized by co-precipitation method. The magnetization curves measured at 2 K show no hysteresis neither remanence for all samples. ZnO:Co grown at low temperature has a positive Curie–Weiss temperature Θ, and ZnO:Co grown at high temperature has a negative Θ. But Al-doped ZnO:Co grown at high temperature has a positive Θ. Positive Curie–Weiss temperature Θ was considered to have relation to the presence of shallow donors in the samples. - Highlights: • Co-doped ZnO and Al, Co co-doped ZnO polycrystalline powders were synthesized. • No hysteresis is observed for all samples. • The Curie–Weiss temperature Θ changes its sign by Al doping. • Positive Θ should be related to shallow donors.

  19. Biaxially textured articles formed by powder metallurgy

    Science.gov (United States)

    Goyal, Amit; Williams, Robert K.; Kroeger, Donald M.

    2003-07-29

    A biaxially textured alloy article having a magnetism less than pure Ni includes a rolled and annealed compacted and sintered powder-metallurgy preform article, the preform article having been formed from a powder mixture selected from the group of mixtures consisting of: at least 60 at % Ni powder and at least one of Cr powder, W powder, V powder, Mo powder, Cu powder, Al powder, Ce powder, YSZ powder, Y powder, Mg powder, and RE powder; the article having a fine and homogeneous grain structure; and having a dominant cube oriented {100} orientation texture; and further having a Curie temperature less than that of pure Ni.

  20. Ultrafine hydrogen storage powders

    Science.gov (United States)

    Anderson, Iver E.; Ellis, Timothy W.; Pecharsky, Vitalij K.; Ting, Jason; Terpstra, Robert; Bowman, Robert C.; Witham, Charles K.; Fultz, Brent T.; Bugga, Ratnakumar V.

    2000-06-13

    A method of making hydrogen storage powder resistant to fracture in service involves forming a melt having the appropriate composition for the hydrogen storage material, such, for example, LaNi.sub.5 and other AB.sub.5 type materials and AB.sub.5+x materials, where x is from about -2.5 to about +2.5, including x=0, and the melt is gas atomized under conditions of melt temperature and atomizing gas pressure to form generally spherical powder particles. The hydrogen storage powder exhibits improved chemcial homogeneity as a result of rapid solidfication from the melt and small particle size that is more resistant to microcracking during hydrogen absorption/desorption cycling. A hydrogen storage component, such as an electrode for a battery or electrochemical fuel cell, made from the gas atomized hydrogen storage material is resistant to hydrogen degradation upon hydrogen absorption/desorption that occurs for example, during charging/discharging of a battery. Such hydrogen storage components can be made by consolidating and optionally sintering the gas atomized hydrogen storage powder or alternately by shaping the gas atomized powder and a suitable binder to a desired configuration in a mold or die.

  1. Thermoluminescent dosimetry of new phosphors of Zn O exposed to beta radiation; Dosimetria termoluminiscente de nuevos fosforos de ZnO expuestos a radiacion beta

    Energy Technology Data Exchange (ETDEWEB)

    Cruz V, C.; Burruel I, S.E.; Grijalva M, H. [UNISON, A.P. 130, Hermosillo, Sonora (Mexico); Barboza F, M.; Bernal, R. [CIF, UNISON, A.P. 5-088, Hermosillo, Sonora (Mexico)

    2004-07-01

    In this work, we report the thermoluminescence dosimetry of a new Zn O phosphor obtained by annealing of Zn S powder precipitated when Zn S films were grown by employing a CBD method. The collected Zn S powder was pressed in a die to form pellets which were subjected to different thermal treatments under air atmosphere. X-ray diffraction (XRD) patterns and energy-dispersive X-ray Spectrometry (EDS) analyses confirmed the transformation of Zn S to Zn O. The phosphors thus obtained were exposed to high doses of beta radiation and their thermoluminescent dosimetry show that these new phosphors are materials suitable to be used in high dose thermoluminescence dosimetry. (Author)

  2. Crystallite-growth, phase transition, magnetic properties, and sintering behaviour of nano-CuFe2O4 powders prepared by a combustion-like process

    International Nuclear Information System (INIS)

    Köferstein, Roberto; Walther, Till; Hesse, Dietrich; Ebbinghaus, Stefan G.

    2014-01-01

    The synthesis of nano-crystalline CuFe 2 O 4 powders by a combustion-like process is described herein. Phase formation and evolution of the crystallite size during the decomposition process of a (CuFe 2 )—precursor gel were monitored up to 1000 °C. Phase-pure nano-sized CuFe 2 O 4 powders were obtained after reaction at 750 °C for 2 h resulting in a crystallite size of 36 nm, which increases to 96 nm after calcining at 1000 °C. The activation energy of the crystallite growth process was calculated as 389 kJ mol −1 . The tetragonal⇄cubic phase transition occurs between 402 and 419 °C and the enthalpy change (ΔH) was found to range between 1020 and 1229 J mol −1 depending on the calcination temperature. The optical band gap depends on the calcination temperature and was found between 2.03 and 1.89 eV. The shrinkage and sintering behaviour of compacted powders were examined. Dense ceramic bodies can be obtained either after conventional sintering at 950 °C or after a two-step sintering process at 800 °C. Magnetic measurements of both powders and corresponding ceramic bodies show that the saturation magnetization rises with increasing calcination-/sintering temperature up to 49.1 emu g −1 (2.1 µ B fu −1 ), whereas the coercivity and remanence values decrease. - Graphical abstract: A cheap one-pot synthesis was developed to obtain CuFe 2 O 4 nano-powders with different crystallite sizes (36–96 nm). The optical band gaps, phase transition temperatures and enthalpies were determined depending on the particle size. The sintering behaviour of nano CuFe 2 O 4 was studied in different sintering procedures. The magnetic behaviour of the nano-powders as well as the corresponding ceramic bodies were investigated. - Highlights: • Eco-friendly and simple synthesis for nano CuFe 2 O 4 powder using starch as polymerization agent. • Monitoring the phase evolution and crystallite growth kinetics during the synthesis. • Determination of the optical band gap

  3. Weighing fluidized powder

    International Nuclear Information System (INIS)

    Adomitis, J.T.; Larson, R.I.

    1980-01-01

    Fluidized powder is discharged from a fluidizing vessel into a container. Accurate metering is achieved by opening and closing the valve to discharge the powder in a series of short-duration periods until a predetermined weight is measured by a load cell. The duration of the discharge period may be increased in inverse proportion to the amount of powder in the vessel. Preferably the container is weighed between the discharge periods to prevent fluctuations resulting from dynamic effects. The gas discharged into the container causes the pressures in the vessel and container to equalize thereby decreasing the rate of discharge and increasing the accuracy of metering as the weight reaches the predetermined value. (author)

  4. ZnO nanoparticles obtained by ball milling technique: Structural, micro-structure, optical and photo-catalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Balamurugan, S., E-mail: scandium.chemistry@gmail.com; Joy, Josny; Godwin, M. Anto; Selvamani, S.; Raja, T. S. Gokul [Advanced Nanomaterials Research Laboratory, Department of Nanotechnology, Noorul Islam Centre for Higher Education, Thuckalay, Kumaracoil - 629 180 (India)

    2016-05-23

    The ZnO nanoparticles were obtained by ball milling of commercial grade ZnO powder at 250 rpm for 20 h and studied their structural, micro-structure, optical and photo-catalytic properties. Due to ball milling significant decrease in lattice parameters and average crystalline size is noticed for the as-milled ZnO nano powder. The HRSEM images of the as-milled powder consist of agglomerated fine spherical nanoparticles in the range of ~10-20 nm. The room temperature PL spectrum of as-milled ZnO nano powder excited under 320 nm reveals two emission bands at ~406 nm (violet emission) and ~639 nm (green emission). Interestingly about 98 % of photo degradation of methylene (MB) by the ZnO catalyst is achieved at 100 minutes of solar light irradiation.

  5. Baking Powder Wars

    OpenAIRE

    Civitello, Linda

    2017-01-01

    How did a mid-nineteenth century American invention, baking powder, replace yeast as a leavening agent and create a culinary revolution as profound as the use of yeast thousands of years ago?The approach was two-pronged and gendered: business archives, U.S. government records and lawsuits revealed how baking powder was created, marketed, and regulated. Women’s diaries and cookbooks—personal, corporate, community, ethnic—from the eighteenth century to internet blogs showed the use women made o...

  6. Evaluation of the magnetocaloric response of nano-sized La0.7Ca0.3Mn1-xNixO3 manganites synthesized by auto-combustion method

    Science.gov (United States)

    Gómez, Adrián; Chavarriaga, Edgar; Supelano, Iván; Parra, Carlos Arturo; Morán, Oswaldo

    2018-05-01

    A systematic study of the dependence of the magnetization on the magnetic field around the ferromagnetic-paramagnetic phase transition temperature is carried out on La0.7Ca0.3Mn1-xNixO3 (x=0, 0.02, 0.07, and 1) samples synthesized by auto-combustion method. The successful substitution of Mn3+ ions by Ni2+ ions in the La0.7Ca0.3MnO3 lattice is corroborated by X-ray diffraction technique. Banerjees criteria, Arrott plots, and the scaling hypothesis are used to analyze the experimental data. It is verified that the Ni-doping increases the operating temperature range for magnetocaloric effect through tuning of the magnetic transition temperature. Probably, the replacement of Mn3+ by Ni2+ ions in the La0.7Ca0.3MnO3 lattice weakens the Mn3+-O-Mn4+ double exchange interaction, which leads to a decrease in the transition temperature and magnetic moment in the samples. The Arrott plots suggest that the phase transition from ferromagnetic to paramagnetic in the nano-sized manganite is of second order. The analysis of the magnetization results show that the maximum magnetic entropy changes observed for x=0, 0.02, 0.07, and 0.1 compositions are 0.85, 0.77, 0.63, and 0.59 J/kg K, under a magnetic field of 1.5 T. These values indicate that the magnetic entropy change achieved for La0.7Ca0.3Mn1-xNixO3 manganites synthesized by auto-combustion method is higher than those reported for other manganites with comparable Ni-doping levels but synthesized by standard solid state reaction. It is also observed that the addition of Ni2+ increases the value of the relative cooling power as compared to that of the parent compound. The highest value of this parameter (˜60 J/kg) is found for a Ni-doping level of 2 % around 230 K in a field of 1.5 T.

  7. Strain modulated defect luminescence in ZnO nanostructures grown on Si substrates

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Hung-Ing; Hsiao, Jui-Ju; Huang, Yi-Jen; Wang, Jen-Cheng [Graduate Institute of Electro-Optical Engineering and Department of Electronic Engineering, Chang Gung University, 259 Wen-Hwa 1st Road, Kwei-Shan, Tao-Yuan 333, Taiwan, ROC (China); Wu, Ya-Fen [Department of Electronic Engineering, Ming Chi University of Technology, Taishan, New Taipei 243, Taiwan, ROC (China); Lu, Bing-Yuh [Department of Electrical Engineering, Tun Gnan University, Shenkeng, New Taipei 222, Taiwan, ROC (China); Nee, Tzer-En, E-mail: neete@mail.cgu.edu.tw [Graduate Institute of Electro-Optical Engineering and Department of Electronic Engineering, Chang Gung University, 259 Wen-Hwa 1st Road, Kwei-Shan, Tao-Yuan 333, Taiwan, ROC (China)

    2015-12-15

    The strain modulated defect green luminescence from ZnO nanostructures grown on silicon substrates has been investigated in-depth. According to the Warren–Averbach Fourier analysis of the X-ray diffraction profiles, both the internal strain and the average crystallite size of the well-ordered nano-size ZnO nanostructures could be subtly modulated by careful adjustment of the aqueous solution of zinc nitrate (Zn(NO{sub 3}){sub 2}) and ammonium hydroxide (NH{sub 3}OH) used in the hydrothermal treatment. Visible defect-related and ultraviolet band-to-band emissions were characterized using temperature-dependent photoluminescence measurements over a broad temperature range from 20 to 300 K. It was found that the thermal-related tensile strain led to the blueshift of the green emission with increasing temperature, while the violet and ultraviolet emissions were thermally insensitive. These spectral observations were substantially corroborated by the deformation potential theory. - Highlights: • The strain modulated defect green luminescence from ZnO nanostructures. • Visible and ultraviolet emissions were characterized using photoluminescence. • The tensile strain led to the blueshift of the green emission. • The spectral observations were corroborated by the deformation potential theory.

  8. Encapsulation of antigen-loaded silica nanoparticles into microparticles for intradermal powder injection.

    Science.gov (United States)

    Deng, Yibin; Mathaes, Roman; Winter, Gerhard; Engert, Julia

    2014-10-15

    Epidermal powder immunisation (EPI) is being investigated as a promising needle-free delivery methods for vaccination. The objective of this work was to prepare a nanoparticles-in-microparticles (nano-in-micro) system, integrating the advantages of nanoparticles and microparticles into one vaccine delivery system for epidermal powder immunisation. Cationic mesoporous silica nanoparticles (MSNP-NH2) were prepared and loaded with ovalbumin as a model antigen. Loading was driven by electrostatic interactions. Ovalbumin-loaded silica nanoparticles were subsequently formulated into sugar-based microparticles by spray-freeze-drying. The obtained microparticles meet the size requirement for EPI. Confocal microscopy was used to demonstrate that the nanoparticles are homogeneously distributed in the microparticles. Furthermore, the silica nanoparticles in the dry microparticles can be re-dispersed in aqueous solution showing no aggregation. The recovered ovalbumin shows integrity compared to native ovalbumin. The present nano-in-micro system allows (1) nanoparticles to be immobilized and finely distributed in microparticles, (2) microparticle formation and (3) re-dispersion of nanoparticles without subsequent aggregation. The nanoparticles inside microparticles can (1) adsorb proteins to cationic shell/surface voids in spray-dried products without detriment to ovalbumin stability, (2) deliver antigens in nano-sized modes to allow recognition by the immune system. Copyright © 2014 Elsevier B.V. All rights reserved.

  9. Effect of wrapped Zn plate on the densification of Al-MWCNTs composites produced by cold pressing and liquid phase sintering

    Energy Technology Data Exchange (ETDEWEB)

    Joo, M.R. [Department of Materials Science and Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of); Choi, H.J. [School of Advanced Materials Engineering, Kookmin University, Seoul 136-702 (Korea, Republic of); Shin, S.E. [Department of Materials Science and Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of); Bae, D.H., E-mail: donghyun@yonsei.ac.kr [Department of Materials Science and Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of)

    2016-09-30

    To produce highly dense and cost-effective Al-multi-walled carbon nanotube (Al-MWCNT) composites, the composite powders are wrapped by a Zn plate and then cold-pressed. The green compacts are then sintered at 550 °C, which shows ~99%density after sintering for 24 h. During sintering, Zn atoms fill the voids at the powder boundaries by capillary action and are then dissolved into the Al matrix because of the high solubility of Zn in Al, thus assisting densification of the composite powder. The Al/Zn-based composites containing 4 vol% MWCNTs show compressive yield strength (~380 MPa) and high work hardening capacity.

  10. Electrochemistry of Zn(II)/Zn on Mg alloy from the N-butyl-N-methylpyrrolidinium dicyanamide ionic liquid

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Ming-Jay, E-mail: martinez730523@yahoo.com.tw [National Synchrotron Radiation Research Center, Hsinchu, Taiwan (China); Lin, Pei-Chiung [Department of Chemistry, National Cheng Kung University, Tainan, Taiwan (China); Chang, Jeng-Kuei, E-mail: jkchang@ncu.edu.tw [Institute of Materials Science and Engineering, National Central University, Taoyuan, Taiwan (China); Chen, Jin-Ming; Lu, Kueih-Tzu [National Synchrotron Radiation Research Center, Hsinchu, Taiwan (China)

    2011-07-01

    Highlights: > Electrodeposition of Zn was successfully demonstrnated in the water- and air-stable BMP-DCA ionic liquid. While ZnCl{sub 2} is insoluble in the BMP-TFSI ionic liquid, it dissolves easily in the BMP-DCA. > Amperometric titration experiments indicated that Zn(II) probably complexed as [Zn(DCA){sub 3}]- with DCA- anion. > Chronoamperometric experiments showed that the electrodeposition of Zn on GC and Mg alloy substrates involved 3D-instantaneous nucleation/growth process. > A lower deposition rate would bring out a more uniform and compact Zn coating layer (which is also thicker) and, consequently, this coating revealed a protection capability for the Mg substrate against corrosion. - Abstract: Electrochemical reaction of Zn(II)/Zn on glassy carbon electrode(GC) and Mg alloy substrates was investigated in the room-temperature ionic liquid, N-butyl-N-methyl-pyrrolidinium dicyanamide (BMP-DCA) containing ZnCl{sub 2} at 323 K. Amperometric titration experiments suggest that Zn(II) reacted with DCA anions forming [Zn(DCA){sub 3}]{sup -} complex anion, which also could be reduced to Zn metal via a single-step electron transfer process. By chronoamperometric measurements, the electrodeposition of Zn on GC and Mg alloy substrates involved three-dimensional instantaneous nucleation under diffusion control at 323 K. The Zn deposits are also systematically characterized by the techniques of powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The Zn layer deposited at a lower current density on Mg alloy substrates was more compact and uniform when compared to that deposited at a higher current density; consequently, this coating revealed a protection capability for the Mg substrate against corrosion.

  11. Characterization of ceramic powder compacts

    International Nuclear Information System (INIS)

    Yanai, K.; Ishimoto, S.; Kubo, T.; Ito, K.; Ishikawa, T.; Hayashi, H.

    1995-01-01

    UO 2 and Al 2 O 3 powder packing structures in cylindrical powder compacts are observed by scanning electron microscopy using polished cross sections of compacts fixed by low viscosity epoxy resin. Hard aggregates which are not destroyed during powder compaction are observed in some of the UO 2 powder compacts. A technique to measure local density in powder compacts is developed based on counting characteristic X-ray intensity by energy dispersive X-ray analysis (EDX). The local density of the corner portion of the powder compact fabricated by double-acting dry press is higher than that of the inner portion. ((orig.))

  12. Preparation, structural and optical characterization of ZnO, ZnO: Al nanopowder

    Energy Technology Data Exchange (ETDEWEB)

    Mohan, R. Raj [Department of ECE, Gojan School of Business and Technology, Chennai (India); Rajendran, K. [Department of Electronics, Government Arts College for Women, Ramanathapuram, TN (India); Sambath, K. [Department of ECS, Sri Krishna Arts and Science College, Coimbatore, TN (India)

    2014-01-28

    In this paper, ZnO and ZnO:Al nanopowders have been synthesized by low cost hydrothermal method. Zinc nitrate, hexamethylenetetramine (HMT) and aluminium nitrate are used as precursors for ZnO and AZO with different molar ratios. The structural and optical characterization of doped and un-doped ZnO powders have been investigated by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDAX), photoluminescence (PL) and ultra violet visible (UV-Vis) absorption studies. The SEM results show that the hydrothermal synthesis can be used to obtain nanoparticles with different morphology. It is observed that the grain size of the AZO nanoparticles increased with increasing of Al concentration. The PL measurement of AZO shows that broad range of green emission around 550nm with high intensity. The green emission resulted mainly because of intrinsic defects.

  13. Shape memory characteristics and mechanical properties of powder metallurgy processed Ti50Ni40Cu10 alloy.

    Science.gov (United States)

    Kim, Yeon-Wook

    2014-10-01

    Ti-Ni-Cu alloy powders were prepared by gas atomization and porous bulk specimens were fabricated by spark plasma sintering (SPS). The microstructure of as-solidified powders exhibited a cellular structure and they contained a high density of nano-sized porosities which were located in the intercellular regions. XRD analysis showed that one-step martensitic transformation of B2-B19 occurred in all alloy powders and SPS specimens. When the martensitic transformation start temperature (M(s)) and austenite transformation finish temperature (A(f)) were determined in order to analyze the dependence of powder size on transformation temperatures, the M(s) increased slightly from -17.5 degrees C to - 14.6 degrees C as increasing the powder size ranging from between 25 and 50 μm to ranging between 100 and 150 μm. However, the M(s) and A(f) of the as-atomized powders is much smaller than those of SPS specimens and the M(s) of porous specimen was about 10.9 degrees C. Loading-unloading compressive tests were carried out to investigate the mechanical properties of porous Ti-Ni-Cu specimen. The specimen was compressed to the strain of 6% at a temperature higher than A,. After unloading, the residual strain was 2.1%. After the compressed specimen was heated to 60 degrees C and held for 30 minutes and then cooled to room temperature, the changes in the length of the specimens were measured. Then it was found that the recovered strain ascribed to shape memory effect was 1.5%.

  14. Magnetically responsive enzyme powders

    Czech Academy of Sciences Publication Activity Database

    Pospišková, K.; Šafařík, Ivo

    2015-01-01

    Roč. 380, APR 2015 (2015), s. 197-200 ISSN 0304-8853 R&D Projects: GA MŠk(CZ) LD13021 Institutional support: RVO:67179843 Keywords : enzyme powders * cross-linking * magnetic modification * magnetic separation * magnetic iron oxides particles * microwave-assisted synthesis Subject RIV: CE - Biochemistry Impact factor: 2.357, year: 2015

  15. Powder neutron diffractometers

    International Nuclear Information System (INIS)

    Adib, M.

    2002-01-01

    Basic properties and applications of powder neutron Diffractometers are described for optimum use of the continuous neutron beams. These instruments are equipped with position sensitive detectors, neutron guide tubes, and both high intensity and high resolution modes of operation are possible .The principles of both direct and Fourier reverse time-of-flight neutron Diffractometers are also given

  16. Low Temperature Powder Coating

    Science.gov (United States)

    2011-02-09

    of volatile organic compounds (VOCs) and hazardous air pollutants (HAPs) • Legacy primers contain hexavalent chrome • Conventional powder coatings...coatings both in laboratory and field service evaluations • LTCPC allows environmental cost reductions through VOC/HAP elimination and hexavalent ... chrome reduction. • The LTCPC process greatly shortens the coating operation (LTCPC cures much more rapidly then conventional wet coatings) resulting in

  17. Laser cladding with powder

    NARCIS (Netherlands)

    Schneider, M.F.; Schneider, Marcel Fredrik

    1998-01-01

    This thesis is directed to laser cladding with powder and a CO2 laser as heat source. The laser beam intensity profile turned out to be an important pa6 Summary rameter in laser cladding. A numerical model was developed that allows the prediction of the surface temperature distribution that is

  18. Effects of serum on cytotoxicity of nano- and micro-sized ZnO particles

    Energy Technology Data Exchange (ETDEWEB)

    Hsiao, I-Lun; Huang, Yuh-Jeen, E-mail: yjhuang@mx.nthu.edu.tw [National Tsing Hua University, Department of Biomedical Engineering and Environmental Sciences (China)

    2013-09-15

    Although an increasing number of in vitro studies are being published regarding the cytotoxicity of nanomaterials, the components of the media for toxicity assays have often varied according to the needs of the scientists. Our aim for this study was to evaluate the influence of serum-in this case, fetal bovine serum-in a cell culture medium on the toxicity of nano-sized (50-70 nm) and micro-sized (<1 {mu}m) ZnO on human lung epithelial cells (A549). The nano- and micro-sized ZnO both exhibited their highest toxicity when exposed to serum-free media, in contrast to exposure in media containing 5 or 10 % serum. This mainly comes not only from the fact that ZnO particles in the serum-free media have a higher dosage-per-cell ratio, which results from large aggregates of particles, rapid sedimentation, absence of protein protection, and lower cell growth rate, but also that extracellular Zn{sup 2+} release contributes to cytotoxicity. Although more extracellular Zn{sup 2+} release was observed in serum-containing media, it did not contribute to nano-ZnO cytotoxicity. Furthermore, non-dissolved particles underwent size-dependent particle agglomeration, resulting in size-dependent toxicity in both serum-containing and serum-free media. A low correlation between cytotoxicity and inflammation endpoints in the serum-free medium suggested that some signaling pathways were changed or induced. Since cell growth, transcription behavior for protein production, and physicochemical properties of ZnO particles all were altered in serum-free media, we recommend the use of a serum-containing medium when evaluating the cytotoxicity of NPs.

  19. Growth, characterization and transport properties of PbxZn1− xS ...

    Indian Academy of Sciences (India)

    The polycrystalline PbZn1−S semiconductor powder with (0 ≤ ≤ 0.5) has been prepared by controlled co-precipitation method from an alkaline medium using thiourea as a sulphide ion source. Pellets are made with these powders applying 10 ton/sq cm pressure and sintered at 800 °C for 2 h in nitrogen atmosphere.

  20. Preparation of sensitized ZnS and its photocatalytic activity under visible light irradiation

    International Nuclear Information System (INIS)

    Zhang Haitao; Chen Xinyi; Li Zhaosheng; Kou Jiahui; Yu Tao; Zou Zhigang

    2007-01-01

    In this paper, sensitized ZnS with visible light driven photocatlytic ability was successfully prepared. The obtained ZnS was characterized by x-ray diffraction, UV-visible diffuse reflectance spectra and Fourier transform infrared spectra. The photocatalytic property of the prepared ZnS was evaluated by decomposing methyl orange (MO). These sensitized ZnS powders with a proper molar ratio showed higher photocatalytic activity than TiO 2 (P25) under visible light (λ > 420 nm) irradiation. A possible explanation for the visible light activity of the prepared ZnS was proposed

  1. Optical, magnetic and structural characterization of Zn1−xCoxO ...

    Indian Academy of Sciences (India)

    attracted considerable attention, both theoretically and experi- mentally, due to their ... C and finally ground to powder. Zn1−x Cox O ... Figure 1. Flowchart for solvothermal synthesis of Zn1−x Cox O (x = 0·038, 0·072 and 0·115) nanoparticles.

  2. Structure and properties of highly toughened biodegradable polylactide/ZnO biocomposite films

    CSIR Research Space (South Africa)

    Jayaramudu, J

    2014-03-01

    Full Text Available Zinc oxide (ZnO) powder was investigated in terms of its use as filler in order to improve the inherent properties of PLA. Biocomposite films of PLA with different loadings of ZnO were prepared by solution casting method. Morphological analyses...

  3. Thermoluminescent dosimetry of new phosphors of Zn O exposed to beta radiation

    International Nuclear Information System (INIS)

    Cruz V, C.; Burruel I, S.E.; Grijalva M, H.; Barboza F, M.; Bernal, R.

    2004-01-01

    In this work, we report the thermoluminescence dosimetry of a new Zn O phosphor obtained by annealing of Zn S powder precipitated when Zn S films were grown by employing a CBD method. The collected Zn S powder was pressed in a die to form pellets which were subjected to different thermal treatments under air atmosphere. X-ray diffraction (XRD) patterns and energy-dispersive X-ray Spectrometry (EDS) analyses confirmed the transformation of Zn S to Zn O. The phosphors thus obtained were exposed to high doses of beta radiation and their thermoluminescent dosimetry show that these new phosphors are materials suitable to be used in high dose thermoluminescence dosimetry. (Author)

  4. Characterization of Ni ferrites powders prepared by plasma arc discharge process

    Energy Technology Data Exchange (ETDEWEB)

    Safari, A. [Department of Materials Science and Engineering, Faculty of Engineering, Shahid Chamran University, Ahvaz (Iran, Islamic Republic of); Gheisari, Kh., E-mail: khgheisari@scu.ac.ir [Department of Materials Science and Engineering, Faculty of Engineering, Shahid Chamran University, Ahvaz (Iran, Islamic Republic of); Farbod, M. [Physics Department, Shahid Chamran University, Ahvaz (Iran, Islamic Republic of)

    2017-01-01

    The aim of this work was to synthesize a single-phase spinel structure from a mixture of zinc, iron and nickel powders by plasma arc discharge method. A mixture of zinc, iron and nickel powders with the appropriate molar ratio was prepared and formed into a cylindrical shape. The synthesis process was performed in air, oxygen and argon atmospheres with the applied arc current of 400 A and pressure of 1 atm. After establishing an arc between the electrodes, the produced powders were collected and their structure and magnetic properties were examined by XRD and VSM, respectively. ZnO as an impurity was appeared in the as-produced powders owing to the high reactivity of zinc atoms, preventing the formation of Ni–Zn ferrite. A pure spinel structure with the highest saturation magnetization (43.8 emu/g) was observed as zinc powders removed completely from the initial mixture. Morphological evaluations using field emission scanning electron microscopy showed that the mean size of fabricated nanoparticles was in the range 100–200 nm and was dependent on the production conditions. - Highlights: • Nanocrystalline Ni ferrite powders are prepared by plasma arc discharge process. • The mean particle size of the as-synthesized ceramic powders is about 100 nm. • The highest saturation magnetization is observed as zinc powders removed completely from the initial mixture.

  5. Method to blend separator powders

    Science.gov (United States)

    Guidotti, Ronald A.; Andazola, Arthur H.; Reinhardt, Frederick W.

    2007-12-04

    A method for making a blended powder mixture, whereby two or more powders are mixed in a container with a liquid selected from nitrogen or short-chain alcohols, where at least one of the powders has an angle of repose greater than approximately 50 degrees. The method is useful in preparing blended powders of Li halides and MgO for use in the preparation of thermal battery separators.

  6. Preparation and characterization of water-soluble ZnSe:Cu/ZnS core/shell quantum dots

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Lei; Cao, Lixin, E-mail: caolixin@ouc.edu.cn; Su, Ge; Liu, Wei; Xia, Chenghui; Zhou, Huajian

    2013-09-01

    The synthesis and luminescent properties of water-soluble ZnSe:Cu/ZnS core/shell quantum dots (QDs) with different shell thickness are reported in this paper. X-ray powder diffraction (XRD) studies present that the ZnSe:Cu/ZnS core/shell QDs with different shell thickness have a cubic zinc-blende structure. The tests of transmission electron microscope (TEM) pictures exhibit that the QDs obtained are spherical-shaped particles and the average grain size increased from 2.7 to 3.8 nm with the growth of ZnS shell. The emission peak position of QDs has a small redshift from 461 to 475 nm with the growth of ZnS shell within the blue spectral window. The photoluminescence (PL) emission intensity and stability of the ZnSe:Cu core d-dots are both enhanced by coating ZnS shell on the surface of core d-dots. The largest PL intensity of the core/shell QDs is almost 3 times larger than that of Cu doped ZnSe quantum dots (ZnSe:Cu d-dots). The redshift of core/shell QDs compared with the core QDs are observed in both the absorption and the photoluminescence excitation spectra.

  7. The effect of powder properties on sintering, microstructure, mechanical strength and degradability of beta-tricalcium phosphate/calcium silicate composite bioceramics

    Energy Technology Data Exchange (ETDEWEB)

    Lin Kaili; Chang Jiang; Shen Ruxiang, E-mail: jchang@mail.sic.ac.c [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China)

    2009-12-15

    The effect of powder properties on sintering, microstructure, mechanical strength and degradability of beta-tricalcium phosphate/Calcium silicate (beta-Ca{sub 3}(PO{sub 4}){sub 2}/CaSiO{sub 3}, beta-TCP/CS) composite bioceramics was investigated. beta-TCP/CS composite powders with a weight ratio of 50:50 were prepared by three different methods: mechanical milling method (TW-A), two-step chemical precipitation method (TW-B) and in situ chemical co-precipitation method (TW-C), and then the three composite powders were uniaxially compacted at 30 MPa, followed by cold isostatic pressing into rectangular-prism-shaped specimens under a pressure of 200 MPa for 15 min, and then sintered at 1150 deg. C for 5 h. The TW-B powders with less agglomerative morphologies and uniform nano-size particles attained 96.14% relative density (RD). A uniform microstructure with about 120 nm grains was observed. Whereas, the samples obtained from TW-A and TW-C powders only reached a RD of 63.08% and 78.86%, respectively. The bending strength of the samples fabricated from TW-B reached 125 MPa, which was more than 3.7 and 1.5 times higher as compared with that of samples obtained from TW-A and TW-C powders, respectively. Furthermore, the degradability of the samples fabricated from TW-B powders was obviously lower than that of the samples fabricated from TW-A and TW-C powders.

  8. Plasma technology for powder particles

    Energy Technology Data Exchange (ETDEWEB)

    Kranz, E. (Technische Hochschule, Ilmenau (German Democratic Republic))

    1983-03-01

    A survey is given of principles and applications of plasma spraying and of powder transformation and generation in plasma considering spheroidization, grain size transformation, powder particle formation, powder reduction, and melting within the power range of 10/sup 3/ to 10/sup 7/ W. The products are applied in many industrial fields such as nuclear engineering, hard metal production, metallurgy, catalysis, and semiconductor techniques.

  9. High-Performance Epoxy-Resin-Bonded Magnets Produced from the Sm2Fe17Nx Powders Coated by Copper and Zinc Metals

    Science.gov (United States)

    Noguchi, Kenji; Machida, Ken-ichi; Adachi, Gin-ya

    2001-04-01

    Fine powders of Sm2Fe17Nx coated with copper metal reduced from CuCl2 and/or zinc metal subsequently derived by photo-decomposition of diethylzinc [Zn(C2H5)2] were prepared, and their magnetic properties were characterized in addition to those of epoxy-resin-bonded magnets produced from the coated powders (Cu/Sm2Fe17Nx, Zn/Sm2Fe17Nx and Zn/Cu/Sm2Fe17Nx). The remanence (Br) and maximum energy product [(\\mathit{BH})max] of double metal-coated Zn/Cu/Sm2Fe17Nx powders were maintained at higher levels than those of single Zn metal-coated Sm2Fe17Nx ones (Zn/Sm2Fe17Nx) even after heat treatment at 673 K since the oxidation resistance and thermal stability were effectively improved by formation of the thick and uniform protection layer on the surface of Sm2Fe17Nx particles. Moreover, the epoxy-resin-bonded magnets produced from the Zn/Cu/Sm2Fe17Nx powders possessed good corrosion resistance in air at 393 K which it resulted in the smaller thermal irreversible flux loss than that of uncoated and single Zn metal-coated Sm2Fe17Nx powders in the temperature range of above 393 K.

  10. Synthesis of Uranium nitride powders using metal uranium powders

    International Nuclear Information System (INIS)

    Yang, Jae Ho; Kim, Dong Joo; Oh, Jang Soo; Rhee, Young Woo; Kim, Jong Hun; Kim, Keon Sik

    2012-01-01

    Uranium nitride (UN) is a potential fuel material for advanced nuclear reactors because of their high fuel density, high thermal conductivity, high melting temperature, and considerable breeding capability in LWRs. Uranium nitride powders can be fabricated by a carbothermic reduction of the oxide powders, or the nitriding of metal uranium. The carbothermic reduction has an advantage in the production of fine powders. However it has many drawbacks such as an inevitable engagement of impurities, process burden, and difficulties in reusing of expensive N 15 gas. Manufacturing concerns issued in the carbothermic reduction process can be solved by changing the starting materials from oxide powder to metals. However, in nitriding process of metal, it is difficult to obtain fine nitride powders because metal uranium is usually fabricated in the form of bulk ingots. In this study, a simple reaction method was tested to fabricate uranium nitride powders directly from uranium metal powders. We fabricated uranium metal spherical powder and flake using a centrifugal atomization method. The nitride powders were obtained by thermal treating those metal particles under nitrogen containing gas. We investigated the phase and morphology evolutions of powders during the nitriding process. A phase analysis of nitride powders was also a part of the present work

  11. Ga-modified nanostructured Zn O: characterization and application in dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Goncalves, Agnaldo S.; Davolos, Marian R.; Antonio, Selma G.; Paiva-Santos, Carlos O. [Universidade Estadual Paulista (IQ/UNESP), Araraquara, SP (Brazil). Inst. de Quimica], e-mails: aagnaldo@iq.unesp.br, cdavolos@iq.unesp.br, selma_ga@yahoo.com.br, cpaiva@iq.unesp.br; Nogueira, Ana F. [Universidade Estadual de Campinas (IQ/UNICAMP), SP (Brazil). Inst. de Quimica], e-mail: anaflavia@iqm.unicamp.br; Masaki, Naruhiko; Yanagida, Shozo [Osaka University, Suita (Japan). Center for Advanced Science and Innovation], e-mails: nmasaki@ casi.osaka-u.ac.jp, s-yanagi@wc4.so-net.ne.jp

    2007-07-01

    Zn O has received great attention in many applications due to its electronic and optical properties. We report on the preparation of Zn O and gallium-containing Zn O (Zn O:Ga) nanoparticles by the precipitation method. The nanoparticles have the wurtzite structure and a high crystallinity. Gallium ions are present as Ga{sup 3+}, as evidenced by the binding energies through XPS. Porosity and surface area of the powder increased under increasing gallium level, explained by the smaller particle size of Zn O:Ga samples compared with Zn O. The estimated optical band gap of Zn O was 3.2 eV, comparable to Zn O:Ga. (author)

  12. Study of de-aggregation of mechanochemically synthesized ZnSe nanoparticles by re-milling in the presence of ZnCl2 solution

    Directory of Open Access Journals (Sweden)

    Marcela Achimovičová

    2013-12-01

    Full Text Available Conventional mechanochemical synthesis of zinc selenide, ZnSe nanoparticles was performed in a planetary ball mill by high-energy milling of zinc (Zn and selenium (Se powders. Mechanochemically synthesized ZnSe was subsequently re-milled in circulation mill in ZnCl2 solution in order to study de-aggregation, physical-chemical and optical properties of ZnSe nanoparticles. The mechanochemically synthesized and re-milled samples were characterized by X-ray diffraction analysis (XRD that confirmed the presence of cubic and hexagonal ZnSe phases. Size of crystallites calculated from XRD patterns has decreased from 50 to 19 nm for cubic ZnSe phase and from 145 to 2.5 nm for hexagonal ZnSe phase after re-milling for 110 min in ZnCl2 solution. Size, phase composition, morphology, and crystallinity of ZnSe nanoparticles were studied by transmission electron microscopy (TEM and selected area electron diffraction (SAED. UV-Vis optical spectroscopy has provided an evidence of blue shift of the re-milled nanocrystalline ZnSe particles from the direct band gap of 2.67 eV characteristic of bulk ZnSe crystals. Colloidal stability of ZnSe nanoparticles dispersions was studied by ? �potential measurements.

  13. Nonstoichiometric Zn Ferrite and ZnFe2O4/Fe2O3 Composite Spheres: Preparation, Magnetic Properties, and Chromium Removal

    Science.gov (United States)

    Hang, Chun-Liang; Yang, Li-Xia; Sun, Chang-Mei; Liang, Ying

    2018-03-01

    Monodisperse and porous nonstoichiometric Zn ferrite can be prepared by a solvothermal method. Such non-Zn ferrite was used to be the precursor for synthesis of ZnFe2O4/Fe2O3 composite via calcination at 600°C for 3 h in air. X-ray powder diffractometer (XRD) and Energy Dispersive Spectrometer (EDS) proved the nonstoichiometry of Zn ferrite synthesized by solvothermal method and the formation of ZnFe2O4/Fe2O3 composite via calcination. TEM image showed that non-Zn ferrite spheres with wormlike nanopore structure were made of primary nanocrystals. BET surface area of non-Zn ferrite was much higher than that of ZnFe2O4/Fe2O3 composite. Saturation magnetization of non-Zn ferrites was significantly higher than that of ZnFe2O4/Fe2O3 composites. Calcination of non-Zn ferrite resulted in the formation of large amount of non-magnetic Fe2O3,which caused a low magnetization of composite. Because of higher BET surface area and higher saturation magnetization, non-Zn ferrite presented better Cr6+ adsorption property than ZnFe2O4/Fe2O3 composites.

  14. Dispersing powders in liquids

    CERN Document Server

    Nelson, RD

    1988-01-01

    This book provides powder technologists with laboratory procedures for selecting dispersing agents and preparing stable dispersions that can then be used in particle size characterization instruments. Its broader goal is to introduce industrial chemists and engineers to the phenomena, terminology, physical principles, and chemical considerations involved in preparing and handling dispersions on a commercial scale. The book introduces novices to: - industrial problems due to improper degree of dispersion; - the nomenclature used in describing particles; - the basic physica

  15. Container for nuclear fuel powders

    International Nuclear Information System (INIS)

    Etheredge, B.F.; Larson, R.I.

    1982-01-01

    A critically safe container is disclosed for the storage and rapid discharge of enriched nuclear fuel material in powder form is disclosed. The container has a hollow, slab-shaped container body that has one critically safe dimension. A powder inlet is provided on one side wall of the body adjacent to a corner thereof and a powder discharge port is provided at another corner of the body approximately diagonal the powder inlet. Gas plenum for moving the powder during discharge are located along the side walls of the container adjacent the discharge port

  16. Processing of ZnO nanocrystals by solochemical technique

    International Nuclear Information System (INIS)

    Gusatti, M.; Speckhahn, R.; Silva, L.A.; Rosario, J.A.; Lima, R.B.; Kuhnen, N.C.; Riella, H.G.; Campos, C.E.M.

    2009-01-01

    In the present work, we report the synthesis of high quality ZnO nanocrystals by solochemical technique. This synthetic strategy has been shown to have advantages over other methods of producing nanostructures in terms of low cost, efficiency, simplicity and uniformity of crystal structure. Zinc chloride solution at room temperature was mixed with sodium hydroxide solution at 50°C to produce ZnO nanocrystals. Transmission electronic microscopy (TEM) and X-ray powder diffraction (XRD) were used to characterize the ZnO nanocrystals obtained. The structure of ZnO was refined by the Rietveld Method from X-ray diffraction data. These methods showed that the product consisted of pure ZnO nanocrystals and has, predominantly, a rod-like morphology. (author)

  17. Obtaining ZnO nanocrystalline through methods of combustion and precipitation

    International Nuclear Information System (INIS)

    Garcia, A.P.; Guaglianoni, W.C.; Cunha, M.A.; Basegio, T.M.; Bergmann, C.P.

    2012-01-01

    Zinc oxide is important technological applications in rubber and industrial paints. The chemical properties and microstructure of ZnO powder depends on the synthesis method employed. In this work, it was obtained nanosized ZnO using different synthesis processes, such as solution combustion and precipitation, varying the concentrations of reactants and the working temperature. The obtained powders were characterized by SEM, BET, XRD, crystallite size determination and thermal analysis (TGA and DTA). It was possible to obtain nanosized ZnO with the methods used. (author)

  18. Identification of phases in zinc alloy powders using electron backscatter diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Perez, Martin G. [Graduate Center for Materials Research, University of Missouri-Rolla, Rolla, MO 65409 (United States); Kenik, Edward A. [Oak Ridge National Laboratory, 100 Bethel Valley Rd., Bldg. 4515, MS-6064, P.O. Box 2008, Oak Ridge, TN 37831 (United States); O' Keefe, Matthew J. [Graduate Center for Materials Research, University of Missouri-Rolla, Rolla, MO 65409 (United States)]. E-mail: mjokeefe@umr.edu; Miller, F. Scott [Graduate Center for Materials Research, University of Missouri-Rolla, Rolla, MO 65409 (United States); Johnson, Benedict [Graduate Center for Materials Research, University of Missouri-Rolla, Rolla, MO 65409 (United States)

    2006-05-25

    Scanning electron microscopy and electron backscatter diffraction (EBSD) were used for the structural characterization of phases in Zn alloy powders. Commercial Zn alloy powders contained additions of <1000 ppm of Bi, In, Al or Mg. Bismuth and In have extremely low solubility in Zn and form intermetallic Bi-In compounds which segregate to the Zn grain boundaries. The Bi-In phases were <0.3 {mu}m in size, had low melting points, and were not abundant enough for EBSD analysis. Increasing the alloying additions 20-40-fold resulted in Bi-In phases >1 {mu}m that could be used for EBSD analysis for phase characterization. Deformation-free microstructures were obtained by mechanical polishing and ion milling. The Zn matrix was characterized as Zn via EBSD. A BiIn{sub 2} phase was identified in the powder microstructures via EBSD. An In phase with 8-9 wt.% Bi was identified using low voltage energy dispersive spectroscopy and closely matched the composition predicted by the Bi-In phase diagram.

  19. Microstructure and mechanical properties of a Mg–Zn–Y alloy produced by a powder metallurgy route

    Energy Technology Data Exchange (ETDEWEB)

    Asgharzadeh, H. [Department of Materials Engineering, Faculty of Mechanical Engineering, University of Tabriz, P.O. Box 51666-16471, Tabriz (Iran, Islamic Republic of); Department of Materials Science and Engineering, Pohang University of Science and Technology, Pohang 790-784 (Korea, Republic of); Yoon, E.Y. [Department of Materials Science and Engineering, Pohang University of Science and Technology, Pohang 790-784 (Korea, Republic of); Chae, H.J.; Kim, T.S. [Korea Institute for Rare Metals, Korea Institute of Industrial Technology, Incheon 406-840 (Korea, Republic of); Lee, J.W. [Korea Institute of Materials Science (KIMS), Changwon 641-831 (Korea, Republic of); Kim, H.S., E-mail: hskim@postech.ac.kr [Department of Materials Science and Engineering, Pohang University of Science and Technology, Pohang 790-784 (Korea, Republic of)

    2014-02-15

    In this paper, a bulk Mg–Zn–Y alloy reinforced by quasicrystalline particles was produced by hot extrusion of rapidly-solidified powders. MgZn{sub 4.3}Y{sub 0.7} powders with different particle sizes were prepared by an inert gas atomizer and then extruded at 380 °C with extrusion ratios of 10:1, 15:1, and 20:1. Microstructural studies were performed using an optical microscope, scanning electron microscope, transmission electron microscope, and X-ray diffraction. The mechanical strength and hardness of the extruded materials were enhanced by employing finer Mg alloy powders. More uniform deformation of powders in extruded billets with good tensile properties was achieved at higher extrusion ratios, especially for finer powders. The high strength of the MgZn{sub 4.3}Y{sub 0.7} alloy was preserved at elevated temperatures due to the presence of icosahedral phase nanoparticles.

  20. Preparation of superconductor precursor powders

    Science.gov (United States)

    Bhattacharya, Raghunath

    1998-01-01

    A process for the preparation of a precursor metallic powder composition for use in the subsequent formation of a superconductor. The process comprises the steps of providing an electrodeposition bath comprising an electrolyte medium and a cathode substrate electrode, and providing to the bath one or more soluble salts of one or more respective metals which are capable of exhibiting superconductor properties upon subsequent appropriate treatment. The bath is continually energized to cause the metallic and/or reduced particles formed at the electrode to drop as a powder from the electrode into the bath, and this powder, which is a precursor powder for superconductor production, is recovered from the bath for subsequent treatment. The process permits direct inclusion of all metals in the preparation of the precursor powder, and yields an amorphous product mixed on an atomic scale to thereby impart inherent high reactivity. Superconductors which can be formed from the precursor powder include pellet and powder-in-tube products.

  1. Application of rapid solidification powder metallurgy processing to prepare Cu–Al–Ni high temperature shape memory alloy strips with high strength and high ductility

    Energy Technology Data Exchange (ETDEWEB)

    Vajpai, S.K., E-mail: vajpaisk@gmail.com [Department of Materials Science and Engineering, Indian Institute of Technology, Kanpur 208016, Uttar Pradesh (India); Dube, R.K., E-mail: rkd@iitk.ac.in [Department of Materials Science and Engineering, Indian Institute of Technology, Kanpur 208016, Uttar Pradesh (India); Sangal, S., E-mail: sangals@iitk.ac.in [Department of Materials Science and Engineering, Indian Institute of Technology, Kanpur 208016, Uttar Pradesh (India)

    2013-05-15

    Cu–Al–Ni high temperature shape memory alloy (HTSMA) strips were successfully prepared from rapid solidified water atomized Cu–Al–Ni pre-alloyed powders via hot densification rolling of unsheathed sintered powder preforms. Finished heat-treated Cu–Al–Ni alloy strips had fine-grained structure, average grain size approximately 16 μm, and exhibited a combination of high strength and high ductility. It has been demonstrated that the redistribution of nano-sized alumina particles, present on the surface as well as inside the starting water atomized Cu–Al–Ni pre-alloyed powder particles, due to plastic deformation of starting powder particles during hot densification rolling resulted in the fine grained microstructure in the finished SMA strips. The finished SMA strips were almost fully martensitic in nature, consisting of a mixture of β{sub 1}{sup ′} and γ{sub 1}{sup ′} martensite. The average fracture strength and fracture strain of the finished SMA strips were 810 MPa and 12%, respectively, and the fractured specimens exhibited primarily micro-void coalescence type ductile nature of fracture. Finished Cu–Al–Ni SMA strips exhibited high characteristic transformation temperatures and an almost 100% one-way shape recovery was obtained in the specimens up to 4% applied deformation pre-strain. The retained two-way shape memory recovery increased with increasing applied training pre-strain, achieving a maximum value of 16.25% at 5% applied training pre-strain.

  2. High power density cell using nanostructured Sr-doped SmCoO3 and Sm-doped CeO2 composite powder synthesized by spray pyrolysis

    Science.gov (United States)

    Shimada, Hiroyuki; Yamaguchi, Toshiaki; Suzuki, Toshio; Sumi, Hirofumi; Hamamoto, Koichi; Fujishiro, Yoshinobu

    2016-01-01

    High power density solid oxide electrochemical cells were developed using nanostructure-controlled composite powder consisting of Sr-doped SmCoO3 (SSC) and Sm-doped CeO2 (SDC) for electrode material. The SSC-SDC nano-composite powder, which was synthesized by spray pyrolysis, had a narrow particle size distribution (D10, D50, and D90 of 0.59, 0.71, and 0.94 μm, respectively), and individual particles were spherical, composing of nano-size SSC and SDC fragments (approximately 10-15 nm). The application of the powder to a cathode for an anode-supported solid oxide fuel cell (SOFC) realized extremely fine cathode microstructure and excellent cell performance. The anode-supported SOFC with the SSC-SDC cathode achieved maximum power density of 3.65, 2.44, 1.43, and 0.76 W cm-2 at 800, 750, 700, and 650 °C, respectively, using humidified H2 as fuel and air as oxidant. This result could be explained by the extended electrochemically active region in the cathode induced by controlling the structure of the starting powder at the nano-order level.

  3. High-performance characteristics of the bonded magnets produced from the Sm2 Fe17 Nx powder stabilized by photo-induced zinc metal coatings

    International Nuclear Information System (INIS)

    Machida, K.; Izumi, H.; Shiomi, A.; Iguchi, M.; Adachi, G.

    1996-01-01

    Finely and uniformly ground powders of Sm 2 Fe 17 N x were stabilized by surface-coating with the zinc metal produced from Zn (C 2 H 5 ) 2 . The epoxy resin-bonded magnets produced from the Zn/Sm 2 Fe 17 N x composite powder provided high-performance permanent magnetic characteristics: (BH)max=∼ 176 kJm -3 . (author)

  4. Synthesis, structural, optical and Raman studies of pure and lanthanum doped ZnSe nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Pushpendra, E-mail: push.nac@gmail.com [Department of Physics, Faculty of Science, Banaras Hindu University, Varanasi 221005 (India); Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 11529, Taiwan (China); Singh, Jai [Department of Physics, Faculty of Science, Banaras Hindu University, Varanasi 221005 (India); Department of Materials Science and Engineering, Pusan National University, 30 Jangjeon-dong, Geumjeong-gu, Busan 609-735 (Korea, Republic of); Pandey, Mukesh Kumar [Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 11529, Taiwan (China); Jeyanthi, C.E. [Research and Development Centre, Bharathiar University, Coimbatore 641 046 (India); Siddheswaran, R. [Department of Materials Science and Engineering, University of Concepcion, Concepcion (Chile); Paulraj, M. [Department of Physics, Faculty of Physical sciences and Mathematics, University of Concepcion, Casilla 160, Concepcion (Chile); Hui, K.N. [Department of Materials Science and Engineering, Pusan National University, 30 Jangjeon-dong, Geumjeong-gu, Busan 609-735 (Korea, Republic of); Hui, K.S., E-mail: kshui@hanyang.ac.kr [Department of Mechanical Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of)

    2014-01-01

    Graphical abstract: - Highlights: • Template-free synthesis of ZnSe and ZnSe:La nanoparticles was developed at low temperature 100 °C. • Cubic ZnSe and ZnSe:La nanoparticles were obtained by chemical route. • As-synthesized ZnSe:La nanoparticles showed higher emission intensity than ZnSe nanoparticles. • Band gap (E{sub g}) of ZnSe nanoparticles was bigger than ZnSe nanoparticles due to nanosized effect. - Abstract: In this work, a simple, effective and reproducible chemical synthetic route for the production of high-quality, pure ZnSe nanoparticles (NPs), and lanthanum-doped ZnSe (ZnSe:La) NPs is presented. The wide bandgap, luminescent pure ZnSe and ZnSe:La NPs has been synthesized at a low temperature (100 °C) in a single template-free step. The size and optical bandgap of the NPs was analyzed from powder X-ray diffraction (XRD), UV–visible (UV–vis) spectroscopy, transmission electron microscopy (TEM), and high resolution transmission electron microscopy (HRTEM). A broad photoluminescence (PL) emission across the visible spectrum has been demonstrated by a systematic blue-shift in emission due to the formation of small nanoparticles. Here, contribution to emission intensity from surface states of NPs increases with La doping. TEM data revealed that the average size of ZnSe and ZnSe:La NPs is 14 and 8 nm, respectively. On the other hand, band gap energy E{sub g} of ZnSe and ZnSe:La NPs were found to be 3.59 eV and 3.65 eV, respectively. Results showed that hydrazine hydrate played multiple roles in the formation of ZnSe and ZnSe:La NPs. A possible reaction mechanism for the growth of NPs is also discussed.

  5. The effects of carbon coating on the electrochemical performances of ZnO in Ni–Zn secondary batteries

    International Nuclear Information System (INIS)

    Long, Wei; Yang, Zhanhong; Fan, Xinming; Yang, Bin; Zhao, Zhiyuan; Jing, Jing

    2013-01-01

    The ZnO samples coated with carbon are successfully synthesized by using a high energy ball milling method. The scanning electron microscopy (SEM) images and energy dispersive spectrometer (EDS) spectra of the carbon-coated ZnO and pure ZnO show that the carbon-coated ZnO (carbon source: glucose, citric acid) samples and the untreated ZnO sample have similar particle size and crystal form. The particles have prismatic microstructure whose sizes are about 100–200 nm. However, the carbon-coated ZnO (carbon source: sucrose) sample has become agglomeration after calcination whose size has been increased to 2–6 μm. The uncoated ZnO powders have more complete crystal shape and they are glazed quadrangular materials, while the carbon coated ZnO particles has a rough surface, which resulted from the growth of carbon coating on ZnO particles. X-ray diffraction (XRD) patterns of the carbon-coated ZnO and the pure ZnO show carbon formed on the surface of ZnO is amorphous. Tafel plot, cyclic voltammetry (CV), AC impedance spectroscopy and galvanostatic charge–discharge measurement are utilized to examine the electrochemical performances of the carbon-coated ZnO. The carbon-coated ZnO (carbon source: glucose) have the most positive steady-state potential and lowest corrosion current density in the zinc electrodes which indicates that it has a good anticorrosion ability. A lower charge platform and a higher discharge platform of carbon-coated ZnO indicate that it have a better charge/discharge performance as anodic material for Ni/Zn cells. A smaller ohmic resistance and charge-transfer resistance imply that the carbon film upon ZnO could greatly decrease the impedance of the reaction process. Meanwhile, the carbon-coated ZnO also showed more excellent cycling performance than pure ZnO. The reason of improvement about electrochemical performance can be ascribed as the unique structure of amorphous carbon layer

  6. Mechanical properties of Mo-Si-B alloys fabricated by using core-shell powder with dispersion of yttria nanoparticles

    Science.gov (United States)

    Byun, Jong Min; Bang, Su-Ryong; Choi, Won June; Kim, Min Sang; Noh, Goo Won; Kim, Young Do

    2017-01-01

    In recent years, refractory materials with excellent high-temperature properties have been in the spotlight as a next generation's high-temperature materials. Among these, Mo-Si-B alloys composed of two intermetallic compound phases (Mo5SiB2 and Mo3Si) and a ductile α-Mo phase have shown an outstanding thermal properties. However, due to the brittleness of the intermetallic compound phases, Mo-Si-B alloys were restricted to apply for the structural materials. So, to enhance the mechanical properties of Mo-Si-B alloys, many efforts to add rare-earth oxide particles in the Mo-Si-B alloy were performed to induce the improvement of strength and fracture toughness. In this study, to investigate the effect of adding nano-sized Y2O3 particles in Mo-Si-B alloy, a core-shell powder consisting of intermetallic compound phases as the core and nano-sized α-Mo and Y2O3 particles surrounding the core was fabricated. Then pressureless sintering was carried out at 1400 °C for 3 h, and the mechanical properties of sintered bodies with different amounts of Y2O3 particles were evaluated by Vickers hardness and 3-point bending test. Vickers hardness was improved by dispersed Y2O3 particles in the Mo-Si-B alloy. Especially, Mo-3Si-1B-1.5Y2O3 alloy had the highest value, 589 Hv. The fracture toughness was measured using Mo-3Si-1B-1.5Y2O3 alloy and the value indicated as 13.5 MPa·√m.

  7. Quenching of surface traps in Mn doped ZnO thin films for enhanced optical transparency

    International Nuclear Information System (INIS)

    Ilyas, Usman; Rawat, R.S.; Roshan, G.; Tan, T.L.; Lee, P.; Springham, S.V.; Zhang, Sam; Fengji Li; Chen, R.; Sun, H.D.

    2011-01-01

    The structural and photoluminescence analyses were performed on un-doped and Mn doped ZnO thin films grown on Si (1 0 0) substrate by pulsed laser deposition (PLD) and annealed at different post-deposition temperatures (500-800 deg. C). X-ray diffraction (XRD), employed to study the structural properties, showed an improved crystallinity at elevated temperatures with a consistent decrease in the lattice parameter 'c'. The peak broadening in XRD spectra and the presence of Mn 2p3/2 peak at ∼640 eV in X-ray Photoelectron Spectroscopic (XPS) spectra of the doped thin films confirmed the successful incorporation of Mn in ZnO host matrix. Extended near band edge emission (NBE) spectra indicated the reduction in the concentration of the intrinsic surface traps in comparison to the doped ones resulting in improved optical transparency. Reduced deep level emission (DLE) spectra in doped thin films with declined PL ratio validated the quenching of the intrinsic surface traps thereby improving the optical transparency and the band gap, essential for optoelectronic and spintronic applications. Furthermore, the formation and uniform distribution of nano-sized grains with improved surface features of Mn-doped ZnO thin films were observed in Field Emission Scanning Electron Microscopy (FESEM) images.

  8. Luminescent characteristics of praseodymium-doped zinc aluminate powders

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez-Perez, C.D.; Garcia-Hipolito, M.; Alvarez-Fregoso, O. [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, Coyoacan, DF (Mexico); Alvarez-Perez, M.A. [Facultad de Odontologia, Universidad Nacional Autonoma de Mexico, Coyoacan, DF (Mexico); Ramos-Brito, F. [Laboratorio de Materiales Optoelectronicos, DIDe, Centro de Ciencias de Sinaloa, Av. De las Americas No. 2771 Nte. Col. Villa Universidad, Culiacan, Sinaloa (Mexico); Falcony, C. [Centro de Investigaciones y Estudios Avanzados del IPN, Departamento de Fisica, Mexico, DF (Mexico)

    2010-02-15

    In this research, we report the cathodoluminescence (CL) and preliminary photoluminescence (PL) properties of praseodymium-doped zinc aluminate powders. ZnAl{sub 2}O{sub 4}:Pr powders were synthesized by a very simple chemical process. X-ray diffraction spectra indicated a cubic spinel crystalline structure with an average crystallite size of 15 nm. CL properties of the powders were studied as a function of the praseodymium concentration and electron-accelerating potential. In this case, all the cathodoluminescent emission spectra showed main peaks located at 494, 535, 611, 646, and 733 nm, which were associated to the electronic transitions {sup 3}P{sub 0}{yields}{sup 3}H{sub 4}, {sup 3}P{sub 0}{yields}{sup 3}H{sub 5}, {sup 3}P{sub 0}{yields}{sup 3}H{sub 6}, {sup 3}P{sub 0}{yields}{sup 3}F{sub 2}, and {sup 3}P{sub 0}{yields}{sup 3}F{sub 4} of the Pr{sup 3+} ions, respectively. A quenching of the CL, with increasing doping concentration, was observed. Also, an increment on cathodoluminescent emission intensity was observed as the accelerating voltage increased. The PL emission spectrum showed similar characteristics to those of the CL spectra. The chemical composition of the powders, as determined by energy dispersive spectroscopy, is also reported. In addition, the surface morphology characteristics of the powders are shown. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  9. Ultra-long Zn{sub 2}SnO{sub 4}-ZnO microwires based gas sensor for hydrogen detection

    Energy Technology Data Exchange (ETDEWEB)

    Fan, Hong [School of Resources and Civil Engineering, Northeastern University, Shenyang 110819 (China); Xu, Shucong [School of Material Science & Engineering, Shandong University, Jinan 250061 (China); Cao, Xianmin; Liu, Daoxi; Yin, Yaoyu; Hao, Haiyong; Wei, Dezhou [School of Resources and Civil Engineering, Northeastern University, Shenyang 110819 (China); Shen, Yanbai, E-mail: shenyanbai@mail.neu.edu.cn [School of Resources and Civil Engineering, Northeastern University, Shenyang 110819 (China)

    2017-04-01

    Highlights: • Ultra-long Zn{sub 2}SnO{sub 4}-ZnO microwires with excellent crystallinity and high yield were obtained. • The maximal length-to-diameter ratio of Zn{sub 2}SnO{sub 4}-ZnO microwires is approximately 1500. • Ultra-long Zn{sub 2}SnO{sub 4}-ZnO microwires show outstanding H{sub 2} sensing properties. - Abstract: Ultra-long Zn{sub 2}SnO{sub 4}-ZnO microwires were synthesized by thermal evaporation of the mixture of SnO{sub 2}, ZnO and C powders. Microstructural characterization by means of X-ray diffraction, scanning electron microscopy and energy dispersive X-ray spectroscopy showed that Zn{sub 2}SnO{sub 4}-ZnO microwires with excellent crystallinity were 2.8–3.2 μm in diameter and 4.0–4.2 mm in length. The maximal length-to-diameter ratio of Zn{sub 2}SnO{sub 4}-ZnO microwires is approximately 1500. H{sub 2} sensing properties showed that Zn{sub 2}SnO{sub 4}-ZnO microwires exhibited not only excellent reversibility to H{sub 2}, but also a good linear relationship between the sensor response and H{sub 2} concentration. The response time and recovery time decreased as the operating temperature increased. The highest sensor response of 9.6 to 1000 ppm H{sub 2} was achieved at an operating temperature of 300 °C. The electron depletion theory was used for explaining H{sub 2} sensing mechanism by the chemical adsorption and reaction of H{sub 2} molecules on the surface of Zn{sub 2}SnO{sub 4}-ZnO microwires.

  10. Diffraction. Powder, amorphous, liquid

    International Nuclear Information System (INIS)

    Sosnowska, I.M.

    1999-01-01

    Neutron powder diffraction is a unique tool to observe all possible diffraction effects appearing in crystal. High-resolution neutron diffractometers have to be used in this study. Analysis of the magnetic structure of polycrystalline materials requires the use of high-resolution neutron diffraction in the range of large interplanar distances. As distinguished from the double axis diffractometers (DAS), which show high resolution only at small interplanar distances, TOF (time-of-flight) diffractometry offers the best resolution at large interplanar distances. (K.A.)

  11. LARC powder prepreg system

    Science.gov (United States)

    Baucom, Robert M.; Marchello, Joseph M.

    1990-01-01

    Thermoplastic prepregs of LARC-TPI have been produced in a fluidized bed unit on spread continuous fiber tows. The powders are melted on the fibers by radiant heating to adhere the polymer to the fiber. This process produces tow prepreg uniformly without imposing severe stress on the fibers or requiring long high temperature residence times for the polymer. Unit design theory and operating correlations have been developed to provide the basis for scale up to commercial operation. Special features of the operation are the pneumatic tow spreader, fluidized bed and resin feed systems.

  12. submitter Preparation and luminescence properties of ZnO:Ga – polystyrene composite scintillator

    CERN Document Server

    Burešová, Hana; Turtos, Rosana Martinez; Jarý, Vítězslav; Mihóková, Eva; Beitlerová, Alena; Pjatkan, Radek; Gundacker, Stefan; Auffray, Etiennette; Lecoq, Paul; Nikl, Martin; Čuba, Václav

    2016-01-01

    Highly luminescent ZnO:Ga-polystyrene composite (ZnO:Ga-PS) with ultrafast subnanosecond decay was prepared by homogeneous embedding the ZnO:Ga scintillating powder into the scintillating organic matrix. The powder was prepared by photo-induced precipitation with subsequent calcination in air and Ar/H2 atmospheres. The composite was subsequently prepared by mixing the ZnO:Ga powder into the polystyrene (10 wt% fraction of ZnO:Ga) and press compacted to the 1 mm thick pellet. Luminescent spectral and kinetic characteristics of ZnO:Ga were preserved. Radioluminescence spectra corresponded purely to the ZnO:Ga scintillating phase and emission of polystyrene at 300-350 nm was absent. These features suggest the presence of non-radiative energy transfer from polystyrene host towards the ZnO:Ga scintillating phase which is confirmed by the measurement of X-ray excited scintillation decay with picosecond time resolution. It shows an ultrafast rise time below the time resolution of the experiment (18 ps) and a single-...

  13. Microwave assisted synthesis of ZnO nanoparticles for lighting and dye removal application

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Vijay, E-mail: vijays_phy@rediffmail.com [Department of Physics, University of Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Gohain, M. [Department of Chemistry, University of Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Som, S.; Kumar, Vinod [Department of Physics, University of Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Bezuindenhoudt, B.C.B. [Department of Chemistry, University of Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Swart, Hendrik C., E-mail: swarthc@ufs.ac.za [Department of Physics, University of Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa)

    2016-01-01

    In this study, we report on the synthesis of ZnO nanoparticles (NPs) via the microwave-assisted technique. The as-synthesized ZnO nanoparticles were annealed at 500 °C for three hours. The ZnO NPs were characterized by X-ray diffraction (XRD) and scanning electron microscopic techniques. XRD results confirmed the formation of as-synthesized ZnO powder oriented along the (101) direction. The Kubelka–Munk function has been employed to determine the band gap of the ZnO powder. ZnO powder has been studied by photoluminescence (PL) before and after annealing to identify the emission of defects in the visible range. The intensity of the PL emission has decreased after annealing. The synthesized ZnO samples were also studied for methyl orange dye removal from waste water. It has been found that the as-synthesized ZnO shows better adsorption behaviour as compared to the annealed sample.

  14. Effect of electrolysis condition of zinc powder production on zinc-silver oxide battery operation

    International Nuclear Information System (INIS)

    Mojtahedi, M.; Goodarzi, M.; Sharifi, B.; Vahdati Khaki, J.

    2011-01-01

    A research conducted to produce zinc powder through electrolysis of alkaline solutions by using various concentrations of KOH and zincate in the bath. Different current densities were applied for each concentration and then, morphological changes of Zn powder batches were examined by scanning electron microscopy. Afterward, an anode electrode was produced from each pack of powder. Thirty-six Zn-AgO battery cells were prepared totally. Discharge parameters of the cells were examined and time-voltage curves were analyzed. Discharge times were investigated for various conditions of Zn deposition and the proper terms were suggested. It has been seen that increase of KOH concentration and decrease of zincate ion in the bath solution will change the zinc morphology and increase the resultant battery discharge time. The longest time of discharge, before reduction of cell voltage to 1.25 V, was 7.91 min. This result was obtained for Zn powder produced in zincate concentration of 0.5 M, KOH concentration of 11 M and current density of 2500 A/m 2 .

  15. Hydro- and solvothermally-prepared ZnO and its catalytic effect on photodegradation of reactive orange 16 dye

    Directory of Open Access Journals (Sweden)

    Simović Bojana

    2014-01-01

    Full Text Available In this work, zinc oxide powders were obtained by two different techniques: hydro- and solvothermal synthesis starting from Zn(NO32 and Zn(CH3COO2, respectively. The influence of synthetic procedure on the structural, microstructural, thermal and photocatalytic properties of the prepared ZnO powders was investigated. Both ZnO samples were further annealed at moderate conditions (300°C to avoid grain growth and to remove traces of impurities. In all four cases a single-phase hexagonal ZnO was confirmed by X-ray powder diffraction. The morphology of prepared ZnO powders was different and it varied from rounded nanograins to microrods. All prepared samples showed higher photocatalytic efficiency in degradation of textile azo-dye Reactive Orange 16(RO16 than the commercial ZnO. In addition, the non-annealed samples had better photocatalytic properties than the commercial Degussa P25 TiO2 powder. [Projekat Ministarstva nauke Republike Srbije, br. III45007, br. ON171032 i br. ON172013

  16. Improved photoluminescence property of CTAB assisted polyaniline-AlZnO nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Mitra, Mousumi; Banerjee, Dipali, E-mail: dipalibanerjeebesu@gmail.com [Department of Physics, Indian Institute of Engineering Science and Technology, Shibpur, Howrah (India); Kargupta, Kajari [Department of Chemical Engineering, Jadavpur University, Kolkata (India); Ganguly, Saibal [Chemical Engineering department, Universiti Teknology Petronas, Tronoh (Malaysia)

    2015-06-24

    Polyaniline-Al doped ZnO ((PANI-AlZnO:: 70:30) nanocomposite was prepared via in situ chemical oxidative polymerization, while the hexagonal powder of AlZnO was synthesized via sol-gel technique, using Hexadecyltrimethylammonium bromide (CTAB) as a capping agent. The prepared nanocomposite was characterized by High resolution transmission electron microscopy (HRTEM), EDAX, X-ray diffraction (XRD) and Fourier transforms infrared (FTIR) spectra. The optical property of the nanomaterials is examined by photoluminescence (PL) spectra analysis. The XRD pattern confirms the formation of Al doped ZnO as well as PANI. The HRTEM images of the composite showed the formation of hexagonal AlZnO embedded in polyaniline matrix. EDAX spectrum shows the compositional analysis of the nanocomposite. FTIR spectra confirm the formation of nanocomposite of PANI and hexagonal AlZnO. The PL intensity of the nanocomposite is improved as compared to pure AlZnO.

  17. The Crystal Structure of Micro- and Nanopowders of ZnS Studied by EPR of Mn2+ and XRD.

    Science.gov (United States)

    Nosenko, Valentyna; Vorona, Igor; Grachev, Valentyn; Ishchenko, Stanislav; Baran, Nikolai; Becherikov, Yurii; Zhuk, Anton; Polishchuk, Yuliya; Kladko, Vasyl; Selishchev, Alexander

    2016-12-01

    The crystal structure of micro- and nanopowders of ZnS doped with different impurities was analyzed by the electron paramagnetic resonance (EPR) of Mn 2+ and XRD methods. The powders of ZnS:Cu, ZnS:Mn, ZnS:Co, and ZnS:Eu with the particle sizes of 5-7 μm, 50-200 nm, 7-10 μm, and 5-7 nm, respectively, were studied. Manganese was incorporated in the crystal lattice of all the samples as uncontrolled impurity or by doping. The Mn 2+ ions were used as EPR structural probes. It is found that the ZnS:Cu has the cubic structure, the ZnS:Mn has the hexagonal structure with a rhombic distortion, the ZnS:Co is the mixture of the cubic and hexagonal phases in the ratio of 1:10, and the ZnS:Eu has the cubic structure and a distorted cubic structure with stacking defects in the ratio 3:1. The EPR technique is shown to be a powerful tool in the determination of the crystal structure for mixed-polytype ZnS powders and powders with small nanoparticles. It allows observation of the stacking defects, which is revealed in the XRD spectra.

  18. Enhancement of ferromagnetic properties in Zn0.98Cu0.02O by additional Co doping

    International Nuclear Information System (INIS)

    Liu, Huilian; Zhang, Xu; Liu, Hongbo; Yang, Jinghai; Liu, Yang; Liu, Xiaoyan; Gao, Ming; Wei, Maobin; Cheng, Xin; Wang, Jian

    2013-01-01

    Highlights: •The samples were synthesized by sol–gel technology to dope up to 3% Co in ZnCuO. •After Co doped into Zn 0.98 Cu 0.02 O sample photoluminescence shows an increase in green emission. •The saturation magnetization increased with Co doping. -- Abstract: Zn 0.98 Cu 0.02 O and Zn 0.95 Cu 0.02 Co 0.03 O powders were synthesized by sol–gel method, and the effects of Co codoping on the structure, optical and magnetic properties of the Zn 0.98 Cu 0.02 O powders were studied in detail. The X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) measurement shows the Zn 0.98 Cu 0.02 O and Zn 0.95 Cu 0.02 Co 0.03 O powders were single phase with the ZnO wurtzite structure, and there was no ferromagnetic-related secondary phase in these powders. Moreover, these powders exhibited ferromagnetism at the room temperature investigated by the magnetic measurement, and the ferromagnetism of the Zn 0.98 Cu 0.02 O and Zn 0.95 Cu 0.02 Co 0.03 O samples were originated from the fact that the Cu ions and Co, Cu ions doped into the ZnO lattices, respectively. In addition, the saturation magnetization (Ms) was significantly increased with Co codoping due to the increased density of oxygen vacancies

  19. Comparative Toxicity of Nanoparticulate CuO and ZnO to Soil Bacterial Communities

    Science.gov (United States)

    Rousk, Johannes; Ackermann, Kathrin; Curling, Simon F.; Jones, Davey L.

    2012-01-01

    The increasing industrial application of metal oxide Engineered Nano-Particles (ENPs) is likely to increase their environmental release to soils. While the potential of metal oxide ENPs as environmental toxicants has been shown, lack of suitable control treatments have compromised the power of many previous assessments. We evaluated the ecotoxicity of ENP (nano) forms of Zn and Cu oxides in two different soils by measuring their ability to inhibit bacterial growth. We could show a direct acute toxicity of nano-CuO acting on soil bacteria while the macroparticulate (bulk) form of CuO was not toxic. In comparison, CuSO4 was more toxic than either oxide form. Unlike Cu, all forms of Zn were toxic to soil bacteria, and the bulk-ZnO was more toxic than the nano-ZnO. The ZnSO4 addition was not consistently more toxic than the oxide forms. Consistently, we found a tight link between the dissolved concentration of metal in solution and the inhibition of bacterial growth. The inconsistent toxicological response between soils could be explained by different resulting concentrations of metals in soil solution. Our findings suggested that the principal mechanism of toxicity was dissolution of metal oxides and sulphates into a metal ion form known to be highly toxic to bacteria, and not a direct effect of nano-sized particles acting on bacteria. We propose that integrated efforts toward directly assessing bioavailable metal concentrations are more valuable than spending resources to reassess ecotoxicology of ENPs separately from general metal toxicity. PMID:22479561

  20. Microstructure, electronic structure and optical properties of combustion synthesized Co doped ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Srinatha, N. [Department of Physics, JB Campus, Bangalore University, Bangalore 560056 (India); Nair, K.G.M. [UGC-DAE-CSR, Kalpakkam Node, Kalpakkam, Kokilamedu 603102 (India); Angadi, Basavaraj, E-mail: brangadi@gmail.com [Department of Physics, JB Campus, Bangalore University, Bangalore 560056 (India)

    2015-10-01

    We report on the microstructure, electronic structure and optical properties of nanocrystalline Zn{sub 1−x}Co{sub x}O (x=0, 0.01, 0.03, 0.05 and 0.07) particles prepared by solution combustion technique using L-Valine as fuel. The detailed structural and micro-structural studies were carried out by XRD, HRTEM and TEM-SAED respectively, which confirms the formation of single phased, nano-sized particles. The electronic structure was determined through NEXAFS and atomic multiplet calculations/simulations performed for various symmetries and valence states of ‘Co’ to determine the valance state, symmetry and crystal field splitting. The correlations between the experimental NEXAFS spectra and atomic multiplet simulations, confirms that, ‘Co’ present is in the 2+ valence state and substituted at the ‘Zn’ site in tetrahedral symmetry with crystal field splitting, 10Dq =−0.6 eV. The optical properties and ‘Co’ induced defect formation of as-synthesized materials were examined by using diffuse reflectance and Photoluminescence spectroscopy, respectively. Red-shift of band gap energy (E{sub g}) was observed in Zn{sub 1−x}Co{sub x}O samples due to Co (0.58 Å) substitution at Zn (0.60 Å) site of the host ZnO. Also, in PL spectra, a prominent pre-edge peak corresponds to ultraviolet (UV) emission around 360–370 nm was observed with Co concentration along with near band edge emission (NBE) of the wide band gap ZnO and all samples show emission in the blue region.

  1. Sintesis de ceramicos de ZnO dopados con praseodimio y cobalto

    Directory of Open Access Journals (Sweden)

    Ana Milena Cruz

    2003-06-01

    Full Text Available Zinc oxide, ZnO, is a very interesting compound in science and electronic ceramics technology. ZnO ceramics containing some additives were reported to show varistor action with excellent nonlinearity in current - voltage characteristics. However, investigations were restricted to the ZnO - Bi2O3 ceramic system. Other type of varistor, which contains praseodymium oxide, also present nonlinear behaviour. In this work, results obtained in the synthesis Zn-Pr-Co powder are shown. In order to determine and control the several stages of the chemical method, potentiometric titration was used. The solid phase obtained was pressed and sintered.

  2. Selective growth of ZnO thin film nanostructures: Structure, morphology and tunable optical properties

    Energy Technology Data Exchange (ETDEWEB)

    Krishnakanth, Katturi Naga; Sunandana, C. S. [School of Physics, University of Hyderabad, Hyderabad-50046 (India); Rajesh, Desapogu, E-mail: rajesh.esapogu@gmail.com, E-mail: mperd@nus.edu.sg [School of Physics, University of Hyderabad, Hyderabad-50046 (India); Dept. of Mechanical Engineering, National University of Singapore (Singapore)

    2016-05-23

    The ZnO nanostructures (spherical, rod shape) have been successfully fabricated via a thermal evaporation followed by dip coating method. The pure, doped ZnO thin films were characterized by X-ray powder diffraction (XRD) and field emission scanning electron microscopy (FESEM) and UV-Vis spectroscopy, respectively. A possible growth mechanism of the spherical, rod shape ZnO nanostructures are discussed. XRD patterns revealed that all films consist of pure ZnO phase and were well crystallized with preferential orientation towards (002) direction. Doping by PVA, PVA+Cu has effective role in the enhancement of the crystalline quality and increases in the band gap.

  3. Biomimetic synthesis of modified calcium phosphate fine powders and their in vitro studies

    Energy Technology Data Exchange (ETDEWEB)

    Gergulova, R., E-mail: rumigg@yahoo.com; Tepavitcharova, S., E-mail: rumigg@yahoo.com; Rabadjieva, D., E-mail: rumigg@yahoo.com; Sezanova, K., E-mail: rumigg@yahoo.com; Ilieva, R., E-mail: rumigg@yahoo.com [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Bl. 11, 1113 Sofia (Bulgaria); Alexandrova, R.; Andonova-Lilova, B. [Institute of Experimental Morphology, Pathology and Anthropology with Museum, BAS, Acad. G. Bonchev Str., Bl. 25, Sofia (Bulgaria)

    2013-12-16

    Biomimetic approach and subsequent high-temperature treatment were used to synthesize ion modified calcium phosphate fine powders. Thus, using Simulated Body Fluid (SBF) as an ion modifier, a bi-phase mixture of ion modified β-tricalcium phosphate and hydroxyapatite (β-TCP + HA) was prepared. The use of SBF electrolyte solution enriched with Mg{sup 2+} or Zn{sup 2+} yielded monophase β-tricalcium phosphate additionally modified with Mg{sup 2+} or Zn{sup 2+} (Mg-β-TCP or Zn-β-TCP). The in vitro behavior of the prepared powders on cell viability and proliferation of murine BALB/c 3T3 fibroblasts and of human Lep 3 cells was studied by MTT test assays and Mosmann method after 72 h incubation. The relative cell viability was calculated.

  4. Sparking deposited ZnO nanoparticles as double-layered photoelectrode in ZnO dye-sensitized solar cell

    Energy Technology Data Exchange (ETDEWEB)

    Hongsith, Kritsada [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Thailand Center of Excellence in Physics (ThEP center), CHE, Bangkok 10400 (Thailand); Hongsith, Niyom [Thailand Center of Excellence in Physics (ThEP center), CHE, Bangkok 10400 (Thailand); School of Science, University of Phayao, Phayao 56000 (Thailand); Wongratanaphisan, Duangmanee; Gardchareon, Atcharawon; Phadungdhitidhada, Surachet [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Thailand Center of Excellence in Physics (ThEP center), CHE, Bangkok 10400 (Thailand); Singjai, Pisith [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Choopun, Supab, E-mail: supab99@gmail.com [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Thailand Center of Excellence in Physics (ThEP center), CHE, Bangkok 10400 (Thailand)

    2013-07-31

    The semiconducting layers of ZnO nanoparticles (ZN), ZnO powder (ZP) and ZnO nanopowder (ZNP) were designed and fabricated for double-layered semiconducting photoelectrode in dye-sensitized solar cells (DSSCs). The under-layer was ZN, which was prepared by simple and cost-effective sparking technique onto F-doped tin oxide (FTO) glass substrate and its thickness was controlled by number of sparking cycles for 0, 10, 25, 50 and 100 rounds under atmospheric pressure. Then, ZP or ZNP was screened on to ZN to form double-layered photoelectrode. Here, the DSSC structures were FTO/double-layered ZnO/Eosin Y/electrolyte/Pt counterelectrode. The best results of DSSCs were observed with J{sub sc} of 4.71 mA/cm{sup 2} and 5.56 mA/cm{sup 2} and photoconversion efficiency of 1.11% and 1.14% at 50 sparking cycles for ZP and ZNP over-layers, respectively. The efficiency enhancement can be explained by combination effects of electron and light scattering. Moreover, the modified equation of short circuit current density was developed and effectively used to explain the efficiency enhancement. - Highlights: • Effect of under-layer thickness is investigated. • Simple and cost-effective sparking technique is used for ZnO nanoparticles. • Efficiency enhancement can be explained by both electron and light scattering. • Modified equation of short circuit current density was developed for enhancement.

  5. Sparking deposited ZnO nanoparticles as double-layered photoelectrode in ZnO dye-sensitized solar cell

    International Nuclear Information System (INIS)

    Hongsith, Kritsada; Hongsith, Niyom; Wongratanaphisan, Duangmanee; Gardchareon, Atcharawon; Phadungdhitidhada, Surachet; Singjai, Pisith; Choopun, Supab

    2013-01-01

    The semiconducting layers of ZnO nanoparticles (ZN), ZnO powder (ZP) and ZnO nanopowder (ZNP) were designed and fabricated for double-layered semiconducting photoelectrode in dye-sensitized solar cells (DSSCs). The under-layer was ZN, which was prepared by simple and cost-effective sparking technique onto F-doped tin oxide (FTO) glass substrate and its thickness was controlled by number of sparking cycles for 0, 10, 25, 50 and 100 rounds under atmospheric pressure. Then, ZP or ZNP was screened on to ZN to form double-layered photoelectrode. Here, the DSSC structures were FTO/double-layered ZnO/Eosin Y/electrolyte/Pt counterelectrode. The best results of DSSCs were observed with J sc of 4.71 mA/cm 2 and 5.56 mA/cm 2 and photoconversion efficiency of 1.11% and 1.14% at 50 sparking cycles for ZP and ZNP over-layers, respectively. The efficiency enhancement can be explained by combination effects of electron and light scattering. Moreover, the modified equation of short circuit current density was developed and effectively used to explain the efficiency enhancement. - Highlights: • Effect of under-layer thickness is investigated. • Simple and cost-effective sparking technique is used for ZnO nanoparticles. • Efficiency enhancement can be explained by both electron and light scattering. • Modified equation of short circuit current density was developed for enhancement

  6. In-situ PXRD studies of ZnO nanoparticle growth: How do various salts influence the hydrothermal growth of ZnO?

    DEFF Research Database (Denmark)

    Bøjesen, Espen Drath

    ZnO is a material of great scientific and everyday relevance; it is used widely in all sorts of application. Synthesis of ZnO nanoparticles can be performed by a wide assortment of methods and a tremendous variety of sizes and shapes, it has been suggested that ZnO is the one known compound showing...... the broadest range of nanostructures. Previously many different in-situ characterization methods have been used to investigate the ZnO formation under various synthesis conditions; these include UV-VIS and SAXS. These methods were primarily used to give information on particle size of ZnO formed using soft...... chemical methods and non-aqueous solvents. In our work we have studied the formation of ZnO during hydrothermal syntheses using in-situ powder X-ray diffraction, thus enabling us to extract crystallographic as well as microstructural information. The data was analyzed using Rietveld refinement and whole...

  7. Nuclear fuel powder transfer device

    International Nuclear Information System (INIS)

    Komono, Akira

    1998-01-01

    A pair of parallel rails are laid between a receiving portion to a molding portion of a nuclear fuel powder transfer device. The rails are disposed to the upper portion of a plurality of parallel support columns at the same height. A powder container is disposed while being tilted in the inside of the vessel main body of a transfer device, and rotational shafts equipped with wheels are secured to right and left external walls. A nuclear powder to be mixed, together with additives, is supplied to the powder container of the transfer device. The transfer device engaged with the rails on the receiving side is transferred toward the molding portion. The wheels are rotated along the rails, and the rotational shafts, the vessel main body and the powder container are rotated. The nuclear powder in the tilted powder container disposed is rotated right and left and up and down by the rotation, and the powder is mixed satisfactory when it reaches the molding portion. (I.N.)

  8. Superconductors by powder metallurgy techniques

    International Nuclear Information System (INIS)

    Pickus, M.R.; Wang, J.L.F.

    1976-05-01

    Fabrication methods for Nb 3 Sn type compounds are described. Information is included on the Bell Telephone process, the General Electric tape process, superconductor stability, the bronze process, powder metallurgy multifilamentary tapes and wires, and current assessment of powder metallurgy superconducting wire

  9. Preparation of zinc ferrite nano powders by high energy wet-milling method and investigation of Crystallites size variation during this process

    International Nuclear Information System (INIS)

    Masoudi, H.; Aftabi, A.; Mozafari, M.; Amighian, J.

    2007-01-01

    In this research work ZnFe 2 O 4 nano powders were prepared by high-energy wet-milling process, using metallic Fe and Zn powders. The process was investigated by XRD technique. 10% of the zinc ferrite was formed after 10 h milling. The as-milled sample was annealed at 500, 550 and 600 d egree C . Ultimately a single sample was obtained at 600 d egree C . Using sherrer's formula, the mean crystallite size of the as-milled and annealed powders were calculated. These were in the range of 17.9 to 20.4 nm.

  10. Inhibition of growth of S. epidermidis by hydrothermally synthesized ZnO nanoplates

    Science.gov (United States)

    Abinaya, C.; Mayandi, J.; Osborne, J.; Frost, M.; Ekstrum, C.; Pearce, J. M.

    2017-07-01

    The antibacterial effect of zinc oxide (ZnO#1) as prepared and annealed (ZnO#2) at 400 °C, Cu doped ZnO (CuZnO), and Ag doped ZnO (AgZnO) nanoplates on Staphylococcus epidermidis was investigated for the inhibition and inactivation of cell growth. The results shows that pure ZnO and doped ZnO samples exhibited antibacterial activity against Staphylococcus epidermidis (S. epidermidis) as compared to tryptic soy broth (TSB). Also it is observed that S. epidermidis was extremely sensitive to treatment with ZnO nanoplates and it is clear that the effect is not purely depend on Cu/Ag. Phase identification of a crystalline material and unit cell dimensions were studied by x-ray powder diffraction (XRD). The scanning electron microscopy (SEM) provides information on sample’s surface topography and the EDX confirms the presence of Zn, O, Cu and Ag. X-ray photo-electron spectroscopy (XPS) was used to analyze the elemental composition and electronic state of the elements that exist within the samples. These studies confirms the formation of nanoplates and the presence of Zn, O, Ag, Cu with the oxidation states  +2, -2, 0 and  +2 respectively. These results indicates promising antibacterial applications of these ZnO-based nanoparticles synthesized with low-cost hydrothermal methods.

  11. Structural and magnetic properties of Ni-Zn and Ni-Zn-Co ferrites

    Energy Technology Data Exchange (ETDEWEB)

    Knyazev, A.V., E-mail: knyazevav@gmail.com [N.I. Lobachevsky State University of Nizhni Novgorod, Gagarin Prospekt 23/2, 603950 Nizhni Novgorod (Russian Federation); Zakharchuk, I.; Lähderanta, E. [Lappeenranta University of Technology, P.O. Box 20, FI-53851 Lappeenranta (Finland); Baidakov, K.V.; Knyazeva, S.S. [N.I. Lobachevsky State University of Nizhni Novgorod, Gagarin Prospekt 23/2, 603950 Nizhni Novgorod (Russian Federation); Ladenkov, I.V. [Joint-stock Company “Research and Production Company “Salut”, Nizhni Novgorod (Russian Federation)

    2017-08-01

    Highlights: • Ni-Zn and Ni-Zn-Co ferrite powders were prepared by the solid-state reaction at 1073 K. • The room temperature saturation magnetizations are 59.7 emu/g for Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} and 57.1 emu/g for Ni{sub 0.5}Zn{sub 0.3}Co{sub 0.2}Fe{sub 2}O{sub 4}. • The coercivity of the samples is found to be much larger than that of bulk ferrites and increases with Co introduction. • The temperature dependences of magnetization exhibit large spin frustration and spin-glass-like behavior. - Abstract: Ni-Zn and Ni-Zn-Co ferrite powders with nominal compositions Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} and Ni{sub 0.5}Zn{sub 0.3}Co{sub 0.2}Fe{sub 2}O{sub 4} were prepared by the solid-state reaction synthesis with periodic regrinding during the calcination at 1073 K. The structure of Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} and Ni{sub 0.5}Zn{sub 0.3}Co{sub 0.2}Fe{sub 2}O{sub 4} was refined assuming space group F d-3m. Scanning electron microscopy revealed the average sizes of the crystalline ferrite particles are 130–630 nm for Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} and 140–350 nm for Ni{sub 0.5}Zn{sub 0.3}Co{sub 0.2}Fe{sub 2}O{sub 4}. The room temperature saturation magnetizations are 59.7 emu/g for Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} and 57.1 emu/g for Ni{sub 0.5}Zn{sub 0.3}Co{sub 0.2}Fe{sub 2}O{sub 4}. The coercivity of the samples is found to be much larger than that of bulk ferrites and increases with Co introduction. The Curie temperature tends to increase upon Zn substitution by Co, as well. The temperature dependences of magnetization measured using zero-field cooled and field cooled protocols exhibit large spin frustration and spin-glass-like behavior.

  12. Light extinction in metallic powder beds: Correlation with powder structure

    International Nuclear Information System (INIS)

    Rombouts, M.; Froyen, L.; Gusarov, A.V.; Bentefour, E.H.; Glorieux, C.

    2005-01-01

    A theoretical correlation between the effective extinction coefficient, the specific surface area, and the chord length distribution of powder beds is verified experimentally. The investigated powder beds consist of metallic particles of several tens of microns. The effective extinction coefficients are measured by a light-transmission technique at a wavelength of 540 nm. The powder structure is characterized by a quantitative image analysis of powder bed cross sections resulting in two-point correlation functions and chord length distributions. The specific surface area of the powders is estimated by laser-diffraction particle-size analysis and by the two-point correlation function. The theoretically predicted tendency of increasing extinction coefficient with specific surface area per unit void volume is confirmed by the experiments. However, a significant quantitative discrepancy is found for several powders. No clear correlation of the extinction coefficient with the powder material and particle size, and morphology is revealed, which is in line with the assumption of geometrical optics

  13. Green method for producing hierarchically assembled pristine porous ZnO nanoparticles with narrow particle size distribution

    Energy Technology Data Exchange (ETDEWEB)

    Escobedo-Morales, A., E-mail: alejandro.escobedo@correo.buap.mx [Facultad de Ingeniería Química, Benemérita Universidad Autónoma de Puebla, C.P. 72570 Puebla, Pue. (Mexico); Téllez-Flores, D.; Ruiz Peralta, Ma. de Lourdes [Facultad de Ingeniería Química, Benemérita Universidad Autónoma de Puebla, C.P. 72570 Puebla, Pue. (Mexico); Garcia-Serrano, J.; Herrera-González, Ana M. [Centro de Investigaciones en Materiales y Metalurgia, Universidad Autónoma del Estado de Hidalgo, Carretera Pachuca Tulancingo Km 4.5, Pachuca, Hidalgo (Mexico); Rubio-Rosas, E. [Centro Universitario de Vinculación y Transferencia de Tecnología, Benemérita Universidad Autónoma de Puebla, C.P. 72570 Puebla, Pue. (Mexico); Sánchez-Mora, E. [Instituto de Física, Benemérita Universidad Autónoma de Puebla, Apdo. Postal J-48, 72570 Puebla, Pue. (Mexico); Olivares Xometl, O. [Facultad de Ingeniería Química, Benemérita Universidad Autónoma de Puebla, C.P. 72570 Puebla, Pue. (Mexico)

    2015-02-01

    A green method for producing pristine porous ZnO nanoparticles with narrow particle size distribution is reported. This method consists in synthesizing ZnO{sub 2} nanopowders via a hydrothermal route using cheap and non-toxic reagents, and its subsequent thermal decomposition at low temperature under a non-protective atmosphere (air). The morphology, structural and optical properties of the obtained porous ZnO nanoparticles were studied by means of powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and nitrogen adsorption–desorption measurements. It was found that after thermal decomposition of the ZnO{sub 2} powders, pristine ZnO nanoparticles are obtained. These particles are round-shaped with narrow size distribution. A further analysis of the obtained ZnO nanoparticles reveals that they are hierarchical self-assemblies of primary ZnO particles. The agglomeration of these primary particles at the very early stage of the thermal decomposition of ZnO{sub 2} powders provides to the resulting ZnO nanoparticles a porous nature. The possibility of using the synthesized porous ZnO nanoparticles as photocatalysts has been evaluated on the degradation of rhodamine B dye. - Highlights: • A green synthesis method for obtaining porous ZnO nanoparticles is reported. • The obtained ZnO nanoparticles have narrow particle size distribution. • This method allows obtaining pristine ZnO nanoparticles avoiding unintentional doping. • A growth mechanism for the obtained porous ZnO nanoparticles is proposed.

  14. Retaining the 3D framework of zinc sponge anodes upon deep discharge in Zn-air cells.

    Science.gov (United States)

    Parker, Joseph F; Nelson, Eric S; Wattendorf, Matthew D; Chervin, Christopher N; Long, Jeffrey W; Rolison, Debra R

    2014-11-26

    We fabricate three-dimensional zinc electrodes from emulsion-cast sponges of Zn powder that are thermally treated to produce rugged monoliths. This highly conductive, 3D-wired aperiodic scaffold achieves 740 mA h gZn(-1) when discharged in primary Zn-air cells (>90% of theoretical Zn capacity). We use scanning electron microscopy and X-ray diffraction to monitor the microstructural evolution of a series of Zn sponges when oxidized in Zn-air cells to specific depths-of-discharge (20, 40, 60, 80% DOD) at a technologically relevant rate (C/40; 4-6 mA cm(-2)). The Zn sponges maintain their 3D-monolithic form factor at all DOD. The cell resistance remains low under all test conditions, indicating that an inner core of metallic Zn persists that 3D-electrically wires the electrode, even to deep DOD.

  15. Photoluminescence analysis of Ce3+:Zn2SiO4 & Li++ Ce3+:Zn2SiO4: phosphors by a sol-gel method

    Science.gov (United States)

    Babu, B. Chandra; Vandana, C. Sai; Guravamma, J.; Rudramadevi, B. Hemalatha; Buddhudu, S.

    2015-06-01

    Here, we report on the development and photoluminescence analysis of Zn2SiO4, Ce3+:Zn2SiO4 & Li+ + Ce3+: Zn2SiO4 novel powder phosphors prepared by a sol-gel technique. The total amount of Ce3+ ions was kept constant in this experiment at 0.05 mol% total doping. The excitation and emission spectra of undoped (Zn2SiO4) and Ce3+ doped Zn2SiO4 and 0.05 mol% Li+ co-doped samples have been investigated. Cerium doped Zn2SiO4 powder phosphors had broad blue emission corresponding to the 2D3/2→2FJ transition at 443nm. Stable green-yellow-red emission has been observed from Zn2SiO4 host matrix and also we have been observed the enhanced luminescence of Li+ co-doped Zn2SiO4:Ce3+. Excitation and emission spectra of these blue luminescent phosphors have been analyzed in evaluating their potential as luminescent screen coating phosphors.

  16. Optimization of parameters in the synthesis of 0.90Pb(Zn1/3Nb2/3)O3–0.10PbTiO3 (PZN-10PT) powders obtained by the mixed oxides method

    Energy Technology Data Exchange (ETDEWEB)

    Raigoza, C.F.V.; Garcia, D.; Eiras, J.A.; Kiminami, R.H.G.A.

    2017-07-01

    Preventing the formation of the pyrochlore phase in the synthesis of PZN-PT powders requires controlling calcination parameters such as temperature, soaking time and atmosphere. These parameters were examined extensively to determine the time and temperature at which the perovskite phase is the majority phase, as well as the atmosphere that facilitates the formation of this phase. A maximum of 74% of perovskite phase was obtained under the following conditions: 1000°C, 4h in nitrogen atmosphere. In this work, we studied the influence of these parameters, which were optimized, on the formation the perovskite phase in PZN-10PT powders synthesized by the conventional solid state method. (Author)

  17. Application of laser in powder metallurgy

    International Nuclear Information System (INIS)

    Tolochko, N.K.

    1995-01-01

    Modern status of works in the field of laser application in powder metallurgy (powders preparation, sintering, coatings formation, powder materials processing) is considered. The attention is paid to the new promising direction in powder products shape-formation technology - laser layer-by-layer selective powders sintering and bulk sintering of packaged layered profiles produced by laser cutting of powder-based sheet blanks. 67 refs

  18. Black powder in gas pipelines

    Energy Technology Data Exchange (ETDEWEB)

    Sherik, Abdelmounam [Saudi Aramco, Dhahran (Saudi Arabia)

    2009-07-01

    Despite its common occurrence in the gas industry, black powder is a problem that is not well understood across the industry, in terms of its chemical and physical properties, source, formation, prevention or management of its impacts. In order to prevent or effectively manage the impacts of black powder, it is essential to have knowledge of its chemical and physical properties, formation mechanisms and sources. The present paper is divided into three parts. The first part of this paper is a synopsis of published literature. The second part reviews the recent laboratory and field work conducted at Saudi Aramco Research and Development Center to determine the compositions, properties, sources and formation mechanisms of black powder in gas transmission systems. Microhardness, nano-indentation, X-ray Diffraction (XRD), X-ray Fluorescence (XRF) and Scanning Electron Microscopy (SEM) techniques were used to analyze a large number of black powder samples collected from the field. Our findings showed that black powder is generated inside pipelines due to internal corrosion and that the composition of black powder is dependent on the composition of transported gas. The final part presents a summary and brief discussion of various black powder management methods. (author)

  19. (TECTONA GRANDIS LEAF POWDER

    Directory of Open Access Journals (Sweden)

    Yash Mishra

    2015-01-01

    Full Text Available In this study, the adsorption potential of Teak (Tectona grandis leaf powder (TLP toremove Methylene blue (MB and Malachite Green (MG dye molecules from aqueoussolution was investigated. Batch experiments were conducted to evaluate the influenceof operational parameters such as, pH (2−9, adsorbent dosage (1−7 g/L, contact time(15−150 minutes and initial dye concentration (20−120 mg/L at stirring speed of 150rpm for the adsorption of MB and MG on TLP. Maximum removal efficiency of 98.4%and 95.1% was achieved for MB and MG dye, respectively. The experimentalequilibrium data were analysed using Langmuir, Freundlich and Temkin isothermmodels and it was found that, it fitted well to the Freundlich isotherm model. Thesurface structure and morphology of the adsorbent was characterized using scanningelectron microscopy (SEM and the presence of functional groups and its interactionwith the dye molecules were analysed using Fourier transform infrared spectroscopy(FTIR. Based on the investigation, it has been demonstrated that the teak leaf powderhas good potential for effective adsorption of methylene blue and malachite green dye.

  20. Low pressure powder injection moulding of stainless steel powders

    Energy Technology Data Exchange (ETDEWEB)

    Zampieron, J.V.; Soares, J.P.; Mathias, F.; Rossi, J.L. [Powder Processing Center CCP, Inst. de Pesquisas Energeticas e Nucleares, Sao Paulo, SP (Brazil); Filho, F.A. [IPEN, Inst. de Pesquisas Energeticas e Nucleares, Cidade Univ., Sao Paulo, SP (Brazil)

    2001-07-01

    Low-pressure powder injection moulding was used to obtain AISI 316L stainless steel parts. A rheological study was undertaken using gas-atomised powders and binders. The binders used were based on carnauba wax, paraffin, low density polyethylene and microcrystalline wax. The metal powders were characterised in terms of morphology, particle size distribution and specific surface area. These results were correlated to the rheological behaviour. The mixture was injected in the shape of square bar specimens to evaluate the performance of the injection process in the green state, and after sintering. The parameters such as injection pressure, viscosity and temperature were analysed for process optimisation. The binders were thermally removed in low vacuum with the assistance of alumina powders. Debinding and sintering were performed in a single step. This procedure shortened considerably the debinding and sintering time. (orig.)

  1. Shock compaction of molybdenum powder

    Science.gov (United States)

    Ahrens, T. J.; Kostka, D.; Vreeland, T., Jr.; Schwarz, R. B.; Kasiraj, P.

    1983-01-01

    Shock recovery experiments which were carried out in the 9 to 12 GPa range on 1.4 distension Mo and appear adequate to compact to full density ( 45 (SIGMA)m) powders were examined. The stress levels, however, are below those calculated to be from 100 to approx. 22 GPa which a frictional heating model predicts are required to consolidate approx. 10 to 50 (SIGMA)m particles. The model predicts that powders that have a distension of m=1.6 shock pressures of 14 to 72 GPa are required to consolidate Mo powders in the 50 to 10 (SIGMA)m range.

  2. An excellent performance anode of ZnFe2O4/flake graphite composite for lithium ion battery

    International Nuclear Information System (INIS)

    Yao, Lingmin; Hou, Xianhua; Hu, Shejun; Tang, Xiaoqin; Liu, Xiang; Ru, Qiang

    2014-01-01

    Highlights: • ZnFe 2 O 4 /flake graphite composite was synt