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Sample records for atomics international aqueous carbonate procelladonna

  1. Atomic Force Microscopy of DNA-wrapped Single-walled Carbon Nanotubes in Aqueous Solution.

    Science.gov (United States)

    Hayashida, Takuya; Umemura, Kazuo

    2016-07-01

    We evaluated hybrids of DNA and single-walled carbon nanotubes (SWNTs) in aqueous solution and in air using atomic force microscopy (AFM). Although intensive AFM observations of these hybrids were previously carried out for samples in air, this is the first report on AFM observations of these hybrids in solution. As expected, diameters of DNA-SWNT hybrids dramatically increased in tris(hydroxymethyl)aminomethane-ethylenediaminetetraacetic acid (TE) buffer solution. The data suggest that DNA molecules maintain their structures even on the SWNT surfaces. Furthermore, we simultaneously observed single DNA-SWNT hybrids using three different AFM modes in air and in the TE buffer solution. Height value of the hybrids was largest in the solution, and lowest for the mode that repulsive force is expected in air. For the bare SWNT molecules, height differences among the three AFM modes were much lower than those of the DNA-SWNT hybrids. DNA molecules adsorbed on SWNT surfaces flexibly changed their morphology as well as DNA molecules on flat surfaces such as mica. This is hopeful results for biological applications of DNA-SWNT hybrids. In addition, our results revealed the importance of the single-molecule approach to evaluate DNA structures on SWNT surfaces. PMID:27045980

  2. Computational insights into the effect of carbon structures at the atomic level for non-aqueous sodium-oxygen batteries

    Science.gov (United States)

    Jiang, H. R.; Wu, M. C.; Zhou, X. L.; Yan, X. H.; Zhao, T. S.

    2016-09-01

    Carbon materials have been widely used to form air cathodes for non-aqueous sodium-oxygen (Nasbnd O2) batteries due to their large specific surface area, high conductivity and low cost. However, the effect of carbon structures at the atomic level remains poorly understood. In this work, a first-principles study is conducted to investigate how representative carbon structures, including graphite (0001) surface, point defects and fractured edge, influence the discharge and charge processes of non-aqueous Nasbnd O2 batteries. It is found that the single vacancy (SV) defect has the largest adsorption energy (5.81 eV) to NaO2 molecule among the structures studied, even larger than that of the NaO2 molecule on NaO2 crystal (2.81 eV). Such high adsorption energy is attributed to two factors: the dangling atoms in SV defects decrease the distance from NaO2 molecules, and the attachment through oxygen atoms increases the electrons transfer. The findings suggest that SV defects can act as the nucleation sites for NaO2 in the discharge process, and increasing the number of SV defects can facilitate the uniform formation of small-sized particles. The uniformly distributed discharge products lower the possibility for pore clogging, leading to an increased discharge capacity and improved cyclability for non-aqueous Nasbnd O2 batteries.

  3. International atomic laboratory

    International Nuclear Information System (INIS)

    Some thirty kilometers to the south-east of Vienna, in the village of Seibersdorf, the International Atomic Energy Agency will have its functional laboratory, the first atomic laboratory to be built by peaceful world-wide co-operation. The building is expected to be completed around the middle of 1960 and the scientific installations will start immediately thereafter. The staff (14 Professional and 24 of the General Service category) for the laboratory are also expected to be engaged at that time and it should be possible to start operating the laboratory in the last quarter of 1960. It is estimated that the construction work will cost about US $400 000 and the total equipment will be worth between $200 000 and $300 000. The United States Government is donating $600 000 for this purpose. The operating costs during 1961, the first full year of operation, will be a little over $240 000. The scope of the laboratory should be limited to certain broad functions. The maximum functions envisaged were: (a) standardization of isotopes and preparation of radioactive standards; (b) calibration and adaptation of measuring equipment; (c) quality control of special materials for nuclear technology; (d) measurements and analysis in connexion with the Agency's safeguards and health and safety programme; and (e) services for Member States which can be undertaken with the facilities needed for the former activities. The idea behind this recommendation will be clear if it is remembered that the research functions of the Agency are governed mostly by its other activities, by its Statutory obligation to encourage and assist peaceful atomic energy work in Member States and establish standards for health and safety and for safeguards against military use

  4. Free energetics of carbon nanotube association in aqueous inorganic NaI salt solutions: Temperature effects using all-atom molecular dynamics simulations.

    Science.gov (United States)

    Ou, Shu-Ching; Cui, Di; Wezowicz, Matthew; Taufer, Michela; Patel, Sandeep

    2015-06-15

    In this study, we examine the temperature dependence of free energetics of nanotube association using graphical processing unit-enabled all-atom molecular dynamics simulations (FEN ZI) with two (10,10) single-walled carbon nanotubes in 3 m NaI aqueous salt solution. Results suggest that the free energy, enthalpy and entropy changes for the association process are all reduced at the high temperature, in agreement with previous investigations using other hydrophobes. Via the decomposition of free energy into individual components, we found that solvent contribution (including water, anion, and cation contributions) is correlated with the spatial distribution of the corresponding species and is influenced distinctly by the temperature. We studied the spatial distribution and the structure of the solvent in different regions: intertube, intratube and the bulk solvent. By calculating the fluctuation of coarse-grained tube-solvent surfaces, we found that tube-water interfacial fluctuation exhibits the strongest temperature dependence. By taking ions to be a solvent-like medium in the absence of water, tube-anion interfacial fluctuation shows similar but weaker dependence on temperature, while tube-cation interfacial fluctuation shows no dependence in general. These characteristics are discussed via the malleability of their corresponding solvation shells relative to the nanotube surface. Hydrogen bonding profiles and tetrahedrality of water arrangement are also computed to compare the structure of solvent in the solvent bulk and intertube region. The hydrophobic confinement induces a relatively lower concentration environment in the intertube region, therefore causing different intertube solvent structures which depend on the tube separation. This study is relevant in the continuing discourse on hydrophobic interactions (as they impact generally a broad class of phenomena in biology, biochemistry, and materials science and soft condensed matter research), and

  5. Atomic data and spectral analysis of carbon, nitrogen, oxygen and silicon ions observed with the International Ultraviolet Explorer

    Science.gov (United States)

    Pradhan, Anil K.

    1992-01-01

    According to the plan presented in the original proposal we have now completed most of the atomic calculations involving collision strengths and rate coefficients for electron impact excitation of C II, N III, and O IV ions. These have been reported in the first two publications appended with this report. We have now moved into the applications phase of the project with the new data being used to analyze the International Ultraviolet Explorer (IUE) observations of a variety of objects, as described in the third publication recently submitted (also appended). The analysis and interpretation of archival data will continue well into the next year with several collaborators that the PI and Co-PI are involved with. In addition, the atomic calculations on Si II have been started.

  6. Atomic matching across internal interfaces

    International Nuclear Information System (INIS)

    The atomic structure of internal interfaces in dense-packed systems has been investigated by high-resolution electron microscopy (HREM). Similarities between the atomic relaxations in heterophase interfaces and certain large-angle grain boundaries have been observed. In both types of interfaces localization of misfit leads to regions of good atomic matching within the interface separated by misfit dislocation-like defects. It appears that, whenever possible, the GB structures assume configurations in which the atomic coordination is not too much different from the ideal lattice. It is suggested that these kinds of relaxations primarily occur whenever the translational periods along the GB are large or when the interatomic distances are incommensurate. Incorporation of low index planes into the GB appears to lead to preferred, i.e. low energy structures, that can be quite dense with good atomic matching across a large fraction of the interface

  7. Aqueous solution dispersement of carbon nanotubes

    Science.gov (United States)

    Kim, Jae-Woo (Inventor); Park, Cheol (Inventor); Choi, Sang H. (Inventor); Lillehei, Peter T. (Inventor); Harrison, Joycelyn S. (Inventor)

    2011-01-01

    Carbon nanotubes (CNTs) are dispersed in an aqueous buffer solution consisting of at least 50 weight percent water and a remainder weight percent that includes a buffer material. The buffer material has a molecular structure defined by a first end, a second end, and a middle disposed between the first and second ends. The first end is a cyclic ring with nitrogen and oxygen heteroatomes, the middle is a hydrophobic alkyl chain, and the second end is a charged group.

  8. Atomic Physics 16: Sixteenth International Conference on Atomic Physics. Proceedings

    International Nuclear Information System (INIS)

    These proceedings represent papers presented at the 16th International Conference on Atomic Physics held in Windsor, Ontario, Canada, in August, 1998. The topics discussed included a wide array of subjects in atomic physics such as atom holography, alignment in atomic collisions, coulomb-interacting particles, muon experiments, x-rays from comets, atomic electron collisions in intense laser fields, spectroscopy of trapped ions, and Bose-Einstein condensates. This conference represents the single most important meeting world wide on fundamental advances in atomic physics. There were 30 papers presented at the conference,out of which 4 have been abstracted for the Energy, Science and Technology database

  9. UNIQUAC interaction parameters for molecules with -OH groups on adjacent carbon atoms in aqueous solution determined by molecular mechanics - glycols, glycerol and glucose

    DEFF Research Database (Denmark)

    Jonsdottir, Svava Osk; Klein, R. A.

    1997-01-01

    UNIQUAC interaction parameters have been determined, using molecular mechanics calculations, for 1,2-ethanediol, 1,2-propanediol, glycerol and glucose with water in aqueous solution. Conformational space for individual pairs of molecules was explored using a stochastic method, the Boltzmann Jump...... difficulties in sampling conformational space in a statistically acceptable manner. As the parameters representinteractions per unit molecular surface area and all of the molecules consist of -CH2OH or -CH2O- units, the values obtained for thewater/1,2-ethanediol system were used to predict VLE data for the......,2-ethanediol, 1,2-propanediol and glycerol, surrounded by different numbers of water molecules. The interaction energy was observed to be linearly dependent on the number of water molecules present. This constant increment means that the additional interaction energy for each water molecule added is the same...

  10. The International Atomic Energy Agency

    Science.gov (United States)

    Dufour, Joanne

    2004-01-01

    The dropping of atomic bombs on Hiroshima and Nagasaki in World War II inaugurated a new era in world history, the atomic age. After the war, the Soviet Union, eager to develop the same military capabilities as those demonstrated by the United States, soon rivaled the U.S. as an atomic and nuclear superpower. Faced by the possibility of…

  11. The International Atomic Energy Agency's safeguards system

    International Nuclear Information System (INIS)

    A system of international safeguards has been established to provide assurance that nuclear materials in civilian use are not diverted from their peaceful purpose. The safeguards system is administered by the International Atomic Energy Agency/Department of Safeguards and devolves from treaties and other international agreements. Inspectors from the Agency verify reports from States about nuclear facilities by audits, observation, and measurements. (author)

  12. Treated Carbon Nanofibers for Storing Energy in Aqueous KOH

    Science.gov (United States)

    Firsich, David W.

    2004-01-01

    A surface treatment has been found to enhance the performances of carbon nanofibers as electrode materials for electrochemical capacitors in which aqueous solutions of potassium hydroxide are used as the electrolytes. In the treatment, sulfonic acid groups are attached to edge plane sites on carbon atoms. The treatment is applicable to a variety of carbon nanofibers, including fibrils and both single- and multiple-wall nanotubes. The reason for choosing nanofibers over powders and other forms of carbon is that nanofibers offer greater power features. In previous research, it was found that the surface treatment of carbon nanofibers increased energy-storage densities in the presence of acid electrolytes. Now, it has been found that the same treatment increases energy-storage densities of carbon nanofibers in the presence of alkaline electrolytes when the carbon is paired with a NiOOH electrode. This beneficial effect varies depending on the variety of carbon substrate to which it is applied. It has been conjectured that the sulfonic acid groups, which exist in a deprotonated state in aqueous KOH solutions, undergo reversible electro-chemical reactions that are responsible for the observed increases in energystorage capacities. The increases can be considerable: For example, in one case, nanofibers exhibited a specific capacitance of 34 Farads per gram before treatment and 172 Farads per gram (an increase of about 400 percent) after treatment. The most promising application of this development appears to lie in hybrid capacitors, which are devices designed primarily for storing energy. These devices are designed to be capable of (1) discharge at rates greater than those of batteries and (2) storing energy at densities approaching those of batteries. A hybrid capacitor includes one electrode like that of a battery and one electrode like that of an electrochemical capacitor. For example, a hybrid capacitor could contain a potassium hydroxide solution as the electrolyte

  13. Internal Active Thermal Control System (IATCS) Sodium Bicarbonate/Carbonate Buffer in an Open Aqueous Carbon Dioxide System and Corollary Electrochemical/Chemical Reactions Relative to System pH Changes

    Science.gov (United States)

    Stegman, Thomas W.; Wilson, Mark E.; Glasscock, Brad; Holt, Mike

    2014-01-01

    The International Space Station (ISS) Internal Active Thermal Control System (IATCS) experienced a number of chemical changes driven by system absorption of CO2 which altered the coolant’s pH. The natural effects of the decrease in pH from approximately 9.2 to less than 8.4 had immediate consequences on system corrosion rates and corrosion product interactions with specified coolant constituents. The alkalinity of the system was increased through the development and implementation of a carbonate/bicarbonate buffer that would increase coolant pH to 9.0 – 10.0 and maintain pH above 9.0 in the presence of ISS cabin concentrations of CO2 up to twenty times higher than ground concentrations. This paper defines how a carbonate/bicarbonate buffer works in an open carbon dioxide system and summarizes the analyses performed on the buffer for safe and effective application in the on-orbit system. The importance of the relationship between the cabin environment and the IATCS is demonstrated as the dominant factor in understanding the system chemistry and pH trends before and after addition of the carbonate/bicarbonate buffer. The paper also documents the corollary electrochemical and chemical reactions the system has experienced and the rationale for remediation of these effects with the addition of the carbonate/bicarbonate buffer.

  14. The atomic level journey from aqueous polyoxometalate to metal oxide

    Energy Technology Data Exchange (ETDEWEB)

    Hou, Yu; Fast, Dylan B.; Ruther, Rose E.; Amador, Jenn M.; Fullmer, Lauren B.; Decker, Shawn R.; Zakharov, Lev N.; Dolgos, Michelle R., E-mail: Michelle.Dolgos@oregonstate.edu; Nyman, May, E-mail: May.Nyman@oregonstate.edu

    2015-01-15

    Aqueous precursors tailored for the deposition of thin film materials are desirable for sustainable, simple, low energy production of advanced materials. Yet the simple practice of using aqueous precursors is complicated by the multitude of interactions that occur between ions and water during dehydration. Here we use lithium polyoxoniobate salts to investigate the fundamental interactions in the transition from precursor cluster to oxide film. Small-angle X-ray scattering of solutions, total X-ray scattering of intermediate gels, and morphological and structural characterization of the lithium niobate thin films reveal the atomic level transitions between these states. The studies show that (1) lithium–[H{sub 2}Nb{sub 6}O{sub 19}]{sup 6−} has drastically different solution behaviour than lithium–[Nb{sub 6}O{sub 19}]{sup 8−}, linked to the precursor salt structure (2) in both compositions, the intermediate gel preserves the polyoxoniobate clusters and show similar local order and (3) the morphology and phases of deposited films reflect the ions behaviour throughout the journey from cluster solution to metal oxide. - Graphical abstract: Aqueous lithium polyoxoniobate salts were used to prepare lithium niobate (LiNbO{sub 3}) thin films. Fundamental studies were performed to investigate the interactions in the transition from precursor cluster to the oxide film. It was found that acid–base and ion-association chemistries of the aqueous and gel systems significantly affect the key processes in this atom-level journey. - Highlights: • Lithium polyoxoniobate clusters were synthesized with control over Li:Nb ratio as precursors for LiNbO{sub 3} films. • X-ray scattering studies in solution and the solid-state revealed differences controlled by Li:Nb ratio. • Film deposition studies revealed phase, composition and morphology is controlled by Li:Nb ratio. • Cluster to film transformation was revealed using total X-ray scattering and TGA.

  15. Photochemical processing of aqueous atmospheric brown carbon

    Science.gov (United States)

    Zhao, R.; Lee, A. K. Y.; Huang, L.; Li, X.; Yang, F.; Abbatt, J. P. D.

    2015-06-01

    Atmospheric brown carbon (BrC) is a collective term for light absorbing organic compounds in the atmosphere. While the identification of BrC and its formation mechanisms is currently a central effort in the community, little is known about the atmospheric removal processes of aerosol BrC. As a result, we report on a series of laboratory studies of photochemical processing of BrC in the aqueous phase, by direct photolysis and OH oxidation. Solutions of ammonium sulfate mixed with glyoxal (GLYAS) or methylglyoxal (MGAS) are used as surrogates for a class of secondary BrC mediated by imine intermediates. Three nitrophenol species, namely 4-nitrophenol, 5-nitroguaiacol and 4-nitrocatechol, were investigated as a class of water-soluble BrC originating from biomass burning. Photochemical processing induced significant changes in the absorptive properties of BrC. The imine-mediated BrC solutions exhibited rapid photo-bleaching with both direct photolysis and OH oxidation, with atmospheric half-lives of minutes to a few hours. The nitrophenol species exhibited photo-enhancement in the visible range during direct photolysis and the onset of OH oxidation, but rapid photo-bleaching was induced by further OH exposure on an atmospheric timescale of an hour or less. To illustrate the atmospheric relevance of this work, we also performed direct photolysis experiments on water-soluble organic carbon extracted from biofuel combustion samples and observed rapid changes in the optical properties of these samples as well. Overall, these experiments indicate that atmospheric models need to incorporate representations of atmospheric processing of BrC species to accurately model their radiative impacts.

  16. Microtribology of aqueous carbon nanotube dispersions

    KAUST Repository

    Kristiansen, Kai De Lange

    2011-09-23

    The tribological behavior of carbon nanotubes (CNTs) in aqueous humic acid (HA) solutions was studied using a surface forces apparatus (SFA) and shows promising lubricant additive properties. Adding CNTs to the solution changes the friction forces between two mica surfaces from "adhesion controlled" to "load controlled" friction. The coefficient of friction with either single-walled (SW) or multi-walled (MW) CNT dispersions is in the range 0.30-0.55 and is independent of the load and sliding velocity. More importantly, lateral sliding promotes a redistribution or accumulation, rather than squeezing out, of nanotubes between the surfaces. This accumulation reduced the adhesion between the surfaces (which generally causes wear/damage of the surfaces), and no wear or damage was observed during continuous shearing experiments that lasted several hours even under high loads (pressures â∼10 MPa). The frictional properties can be understood in terms of the Cobblestone Model where the friction force is related to the fraction of the adhesion energy dissipated during impacts of the nanoparticles. We also develop a simple generic model based on the van der Waals interactions between particles and surfaces to determine the relation between the dimensions of nanoparticles and their tribological properties when used as additives in oil- or water-based lubricants. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Internal friction in martensitic carbon steels

    Energy Technology Data Exchange (ETDEWEB)

    Hoyos, J.J., E-mail: jjhoyos@unal.edu.co [Grupo de Ciencia y Tecnologia de los Materiales, Universidad Nacional de Colombia, Sede Medellin, Carrera 80 Numero 65-223, Medellin (Colombia); Ghilarducci, A.A., E-mail: friccion@cab.cnea.gov.ar [Centro Atomico Bariloche, Comision Nacional de Energia Atomica, Instituto Balseiro-Universidad Nacional de Cuyo, Consejo Nacional de Investigaciones Cientificas y Tecnologicas, Av. Bustillo 9500, 8400 Bariloche RN (Argentina); Salva, H.R., E-mail: salva@cab.cnea.gov.ar [Centro Atomico Bariloche, Comision Nacional de Energia Atomica, Instituto Balseiro-Universidad Nacional de Cuyo, Consejo Nacional de Investigaciones Cientificas y Tecnologicas, Av. Bustillo 9500, 8400 Bariloche RN (Argentina); Chaves, C.A., E-mail: cachaves@unal.edu.co [Grupo de Ciencia y Tecnologia de los Materiales, Universidad Nacional de Colombia, Sede Medellin, Carrera 80 Numero 65-223, Medellin (Colombia); Velez, J.M., E-mail: jmvelez@unal.edu.co [Grupo de Ciencia y Tecnologia de los Materiales, Universidad Nacional de Colombia, Sede Medellin, Carrera 80 Numero 65-223, Medellin (Colombia)

    2009-09-15

    This paper proposes relationships between the internal friction and the microstructure of two steels containing 0.626 and 0.71 wt.% carbon. The steels were annealed at 1093 K for 5 min, quenched into water and tempered for 10 min at 423, 573 and 723 K. Internal friction was measured by using a forced vibration pendulum, in a temperature range from 100 to 450 K. The internal friction spectrum is decomposed into four peaks: P1 at 215 K, P2 at 235 K, P3 at 260 K and P4 at 380 K for 3 Hz. Peak P1 is attributed to the interactions between dislocations and carbon atoms. Peak P2 is related to the interaction between dislocations and carbide. Peak P3 is related to the generations of kink - pairs along edge dislocations. Peak P4 is attributed to epsilon carbide precipitation.

  18. Internal friction in martensitic carbon steels

    International Nuclear Information System (INIS)

    This paper proposes relationships between the internal friction and the microstructure of two steels containing 0.626 and 0.71 wt.% carbon. The steels were annealed at 1093 K for 5 min, quenched into water and tempered for 10 min at 423, 573 and 723 K. Internal friction was measured by using a forced vibration pendulum, in a temperature range from 100 to 450 K. The internal friction spectrum is decomposed into four peaks: P1 at 215 K, P2 at 235 K, P3 at 260 K and P4 at 380 K for 3 Hz. Peak P1 is attributed to the interactions between dislocations and carbon atoms. Peak P2 is related to the interaction between dislocations and carbide. Peak P3 is related to the generations of kink - pairs along edge dislocations. Peak P4 is attributed to epsilon carbide precipitation.

  19. International Atomic Energy Agency: Highlights of activities

    International Nuclear Information System (INIS)

    This document provides a brief, well-illustrated summary of the activities of the International Atomic Energy Agency in the months up to September 1992. Especially mentioned are the programmes to enhance the safety of nuclear power, from the study of nuclear reactors to assessing the radiological consequences of reactor accidents, and the areas of non-proliferation and safeguards

  20. International Atomic Energy Agency. Highlights of activities

    International Nuclear Information System (INIS)

    This document provides a brief, well-illustrated summary of the activities of the International Atomic Energy Agency in the months up to September 1991. Especially mentioned are the programmes to enhance the safety of nuclear power, from the study of nuclear reactors to assessing the radiological consequences of reactor accidents, and the areas of non-proliferation and safeguards

  1. Hydrogen-atom attack on methyl viologen in aqueous solution studied by pulse radiolysis

    International Nuclear Information System (INIS)

    Using hydrogen at high pressures of up to 150 bar as an OH scavenger in aqueous MV2+ solutions (pH 1) it is possible to differentiate between two kinds of transient formed simultaneously by H-atom attack on methyl viologen. One of them is assigned to an H adduct on the N atom, MV+H+, with absorption bands identical to those of the radical cation, MV+. The MV+H+ species deprotonates forming the long-lived radical cation, MV+. The second type of transient produced is attributed to an H-adduct on the ring carbon, MV2+H, decaying by second-order kinetics. The formation of MV+ by electron transfer from the propan-2-ol radical has been reinvestigated (pH 0 to 7); its absorption spectrum does not change in this pH range. Rate constants and molar extinction coefficients are presented. (U.K.)

  2. Adsorption of EDTA on activated carbon from aqueous solutions

    International Nuclear Information System (INIS)

    In this study, the adsorption of EDTA on activated carbon from aqueous solutions has been investigated in a batch stirred cell. Experiments have been carried out to investigate the effects of temperature, EDTA concentration, pH, activated carbon mass and particle size on EDTA adsorption. The experimental results manifest that the EDTA adsorption rate increases with its concentration in the aqueous solutions. EDTA adsorption also increases with temperature. The EDTA removal from the solution increases as activated carbon mass increases. The Langmuir and Freundlich equilibrium isotherm models are found to provide a good fitting of the adsorption data, with R2 = 0.9920 and 0.9982, respectively. The kinetic study shows that EDTA adsorption on the activated carbon is in good compliance with the pseudo-second-order kinetic model. The thermodynamic parameters (Ea, ΔG0, ΔH0, ΔS0) obtained indicate the endothermic nature of EDTA adsorption on activated carbon.

  3. Oxygen atom loss coefficient of carbon nanowalls

    Energy Technology Data Exchange (ETDEWEB)

    Mozetic, Miran, E-mail: miran.mozetic@guest.arnes.si [Jozef Stefan Institute, Jamova cesta 39, 1000 Ljubljana (Slovenia); Vesel, Alenka [Jozef Stefan Institute, Jamova cesta 39, 1000 Ljubljana (Slovenia); Stoica, Silviu Daniel; Vizireanu, Sorin; Dinescu, Gheorghe [National Institute for Laser, Plasma and Radiation Physics, 409 Atomistilo Street, PO Box MG-36, Magurele, Bucharest 077125 (Romania); Zaplotnik, Rok [Jozef Stefan Institute, Jamova cesta 39, 1000 Ljubljana (Slovenia)

    2015-04-01

    Highlights: • Atomic oxygen loss coefficient on carbon nanowalls (CNWs) was evaluated. • Atomic oxygen loss coefficient of CNW is the largest among any known materials. • Surface atom loss is a major loss mechanism at room temperatures. - Abstract: Extremely high values of atomic oxygen loss coefficient on carbon nanowall (CNW) surface are reported. CNW layers consisting of interconnected individual nanostructures with average length of 1.1 μm, average thickness of 66 nm and surface density of 3 CNW/μm{sup 2} were prepared by plasma jet enhanced chemical-vapor deposition using C{sub 2}H{sub 2}/H{sub 2}/Ar gas mixtures. The samples were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM), Raman spectrometry (RS) as well as X-ray photoelectron spectroscopy (XPS). The surface loss coefficient was measured at room temperature in a flowing afterglow at different densities of oxygen atoms supplied from inductively coupled radiofrequency O{sub 2} plasma. The RF generator operated at 13.56 MHz and different nominal powers up to 900 W corresponding to different O-atom density in the afterglow up to 1.3 × 10{sup 21} m{sup −3}. CNW and several different samples of known coefficients for heterogeneous surface recombination of neutral oxygen atoms have been placed separately in the afterglow chamber and the O-atom density in their vicinity was measured with calibrated catalytic probes. Comparison of measured results allowed for determination of the loss coefficient for CNWs and the obtained value of 0.59 ± 0.03 makes this material an extremely effective sink for O-atoms.

  4. Atomic resolution studies of carbonic anhydrase II

    International Nuclear Information System (INIS)

    The structure of human carbonic anhydrase II has been solved with a sulfonamide inhibitor at 0.9 Å resolution. Structural variation and flexibility is seen on the surface of the protein and is consistent with the anisotropic ADPs obtained from refinement. Comparison with 13 other atomic resolution carbonic anhydrase structures shows that surface variation exists even in these highly ordered isomorphous crystals. Carbonic anhydrase has been well studied structurally and functionally owing to its importance in respiration. A large number of X-ray crystallographic structures of carbonic anhydrase and its inhibitor complexes have been determined, some at atomic resolution. Structure determination of a sulfonamide-containing inhibitor complex has been carried out and the structure was refined at 0.9 Å resolution with anisotropic atomic displacement parameters to an R value of 0.141. The structure is similar to those of other carbonic anhydrase complexes, with the inhibitor providing a fourth nonprotein ligand to the active-site zinc. Comparison of this structure with 13 other atomic resolution (higher than 1.25 Å) isomorphous carbonic anhydrase structures provides a view of the structural similarity and variability in a series of crystal structures. At the center of the protein the structures superpose very well. The metal complexes superpose (with only two exceptions) with standard deviations of 0.01 Å in some zinc–protein and zinc–ligand bond lengths. In contrast, regions of structural variability are found on the protein surface, possibly owing to flexibility and disorder in the individual structures, differences in the chemical and crystalline environments or the different approaches used by different investigators to model weak or complicated electron-density maps. These findings suggest that care must be taken in interpreting structural details on protein surfaces on the basis of individual X-ray structures, even if atomic resolution data are available

  5. Carbon/Carbon Pistons for Internal Combustion Engines

    Science.gov (United States)

    Taylor, A. H.

    1986-01-01

    Carbon/carbon piston performs same function as aluminum pistons in reciprocating internal combustion engines while reducing weight and increasing mechanical and thermal efficiencies of engine. Carbon/carbon piston concept features low piston-to-cylinder wall clearance - so low piston rings and skirts unnecessary. Advantages possible by negligible coefficient of thermal expansion of carbon/carbon.

  6. Detection of gas atoms with carbon nanotubes

    Science.gov (United States)

    Arash, B.; Wang, Q.

    2013-05-01

    Owning to their unparalleled sensitivity resolution, nanomechanical resonators have excellent capabilities in design of nano-sensors for gas detection. The current challenge is to develop new designs of the resonators for differentiating distinct gas atoms with a recognizably high sensitivity. In this work, the characteristics of impulse wave propagation in carbon nanotube-based sensors are investigated using molecular dynamics simulations to provide a new method for detection of noble gases. A sensitivity index based on wave velocity shifts in a single-walled carbon nanotube, induced by surrounding gas atoms, is defined to explore the efficiency of the nano-sensor. The simulation results indicate that the nano-sensor is able to differentiate distinct noble gases at the same environmental temperature and pressure. The inertia and the strengthening effects by the gases on wave characteristics of carbon nanotubes are particularly discussed, and a continuum mechanics shell model is developed to interpret the effects.

  7. Carbonated aqueous media for quench heat treatment of steels

    Science.gov (United States)

    Nayak, U. Vignesh; Rao, K. M. Pranesh; Pai, M. Ashwin; Prabhu, K. Narayan

    2016-07-01

    Distilled water and polyalkylene glycol (PAG)-based aqueous quenchants of 5 and 10 vol.% with and without carbonation were prepared and used as heat transfer media during immersion quenching. Cooling curves were recorded during quenching of an inconel 600 cylindrical probe instrumented with multiple thermocouples. It was observed that the vapor stage duration was prolonged and the wetting front ascended uniformly for quenching with carbonated media. The cooling data were analyzed by determining the critical cooling parameters and by estimating the spatially dependent probe/quenchant interfacial heat flux transients. The study showed significantly reduced values of heat transfer rate for carbonated quenchants compared to quenchants without carbonation. Further, the reduction was more pronounced in the case of PAG-based carbonated quenchants than carbonated distilled water. The results also showed the dependence of heat transfer characteristics of the carbonated media on polymer concentration. The effect of quench uniformity on the microstructure of the material was assessed.

  8. Sugars as the optimal biosynthetic carbon substrate of aqueous life throughout the universe

    Science.gov (United States)

    Weber, A. L.

    2000-01-01

    Our previous analysis of the energetics of metabolism showed that both the biosynthesis of amino acids and lipids from sugars, and the fermentation of organic substrates, were energetically driven by electron transfer reactions resulting in carbon redox disproportionation (Weber, 1997). Redox disproportionation--the spontaneous (energetically favorable) direction of carbon group transformation in biosynthesis--is brought about and driven by the energetically downhill transfer of electron pairs from more oxidized carbon groups (with lower half-cell reduction potentials) to more reduced carbon groups (with higher half-cell reduction potentials). In this report, we compare the redox and kinetic properties of carbon groups in order to evaluate the relative biosynthetic capability of organic substrates, and to identify the optimal biosubstrate. This analysis revealed that sugars (monocarbonyl alditols) are the optimal biosynthetic substrate because they contain the maximum number of biosynthetically useful high energy electrons/carbon atom while still containing a single carbonyl group needed to kinetically facilitate their conversion to useful biosynthetic intermediates. This conclusion applies to aqueous life throughout the Universe because it is based on invariant aqueous carbon chemistry--primarily, the universal reduction potentials of carbon groups.

  9. Solubility of carbon dioxide in aqueous piperazine solutions

    NARCIS (Netherlands)

    Derks, P. W. J.; Dijkstra, H. B. S.; Hogendoorn, J. A.; Versteeg, G. F.

    2005-01-01

    In the present work, new experimental data are presented on the solubility of carbon dioxide in aqueous piperazine solutions, for concentrations of 0.2 and 0.6 molar piperazine and temperatures of 25, 40, and 70°C respectively. The present data, and other data available in the literature, were corr

  10. Nanoporous activated carbon cloth for capacitive deionization of aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Han-Jun [Department of Materials Science, Hanseo University, Seosan, 352-820 (Korea, Republic of); Lee, Jong-Ho [Department of Chemistry, Hanseo University, Seosan, 352-820 (Korea, Republic of); Ahn, Hong-Joo [Korea Atomic Energy Research Institute, Daejeon, 305-600 (Korea, Republic of); Jeong, Yongsoo [Korea Institute of Machinery and Materials, Changwon, 641-010 (Korea, Republic of); Kim, Young-Jig [Department of Metallurgical Engineering, Sungkyunkwan University, Suwon, 440-746 (Korea, Republic of); Chi, Choong-Soo [School of Advanced Materials Engineering, Kookmin University, Seoul, 136-702 (Korea, Republic of)]. E-mail: cschi@kookmin.ac.kr

    2006-09-25

    Activated nanostructured-carbon cloths with a high ratio of surface area to volume are used as electrode for capacitive deionization. The electrochemical properties on capacitive deionization for NaCl solution have been investigated to improve efficiency of capacitive deionization properties from aqueous solution, employing chemical surface-modification by etching in alkaline and acidic solution. The removal efficiency of inorganic salts of activated carbon cloths by chemical modification significantly increased. Specially the carbon cloth surface modified in HNO{sub 3} showed an effect of improvement in the CDI efficiency due to not only ion adsorption by an electric double layer, but also electron transfer by Faradaic reaction.

  11. Detection of gas atoms with carbon nanotubes

    OpenAIRE

    Arash, B.; Wang, Q.

    2013-01-01

    Owning to their unparalleled sensitivity resolution, nanomechanical resonators have excellent capabilities in design of nano-sensors for gas detection. The current challenge is to develop new designs of the resonators for differentiating distinct gas atoms with a recognizably high sensitivity. In this work, the characteristics of impulse wave propagation in carbon nanotube-based sensors are investigated using molecular dynamics simulations to provide a new method for detection of noble gases....

  12. Atom probe tomography (APT) of carbonate minerals.

    Science.gov (United States)

    Pérez-Huerta, Alberto; Laiginhas, Fernando; Reinhard, David A; Prosa, Ty J; Martens, Rich L

    2016-01-01

    Atom probe tomography (APT) combines the highest spatial resolution with chemical data at atomic scale for the analysis of materials. For geological specimens, the process of field evaporation and molecular ion formation and interpretation is not yet entirely understood. The objective of this study is to determine the best conditions for the preparation and analysis by APT of carbonate minerals, of great importance in the interpretation of geological processes, focusing on the bulk chemical composition. Results show that the complexity of the mass spectrum is different for calcite and dolomite and relates to dissimilarities in crystalochemical parameters. In addition, APT bulk chemistry of calcite closely matches the expected stoichiometry but fails to provide accurate atomic percentages for elements in dolomite under the experimental conditions evaluated in this work. For both calcite and dolomite, APT underestimates the amount of oxygen based on their chemical formula, whereas it is able to detect small percentages of elemental substitutions in crystal lattices. Overall, our results demonstrate that APT of carbonate minerals is possible, but further optimization of the experimental parameters are required to improve the use of atom probe tomography for the correct interpretation of mineral geochemistry. PMID:26519815

  13. Kinetics of Aqueous Leaching and Carbonization of Steelmaking Slag

    Science.gov (United States)

    Lekakh, S. N.; Rawlins, C. H.; Robertson, D. G. C.; Richards, V. L.; Peaslee, K. D.

    2008-02-01

    Sequestration of carbon dioxide by steelmaking slag was studied in an atmospheric three-phase system containing industrial slag particles, water, and CO2 gas. Batch-type reactors were used to measure the rate of aqueous alkaline leaching and slag particle carbonization independently. Four sizes of slag particles were tested for the Ca leaching rate in deionized water at a constant 7.5 pH in an argon atmosphere and for carbonate conversion with CO2 bubbled through an aqueous suspension. Conversion data (fraction of Ca leached or converted to carbonate) were evaluated to determine the rate-limiting step based on the shrinking core model. For Ca leaching, the chemical reaction is the controlling mechanism during the initial period of time, which then switches to diffusion through the developed porous layer as the rate-limiting step. Carbonate conversion proceeded much slower than leaching conversion and was found to be limited by diffusion through the product calcium carbonate layer. The calculated value of diffusivity was found to be 5 × 10-9 cm2/s, which decreased by an order of magnitude with increasing carbonization conversion as a result of changing density of the product layer. The experimental data fit the shrinking core model well after correction for the particle specific surface area.

  14. Carbon nanotube atomic force microscopy probes

    Science.gov (United States)

    Yamanaka, Shigenobu; Okawa, Takashi; Akita, Seiji; Nakayama, Yoshikazu

    2005-05-01

    We have developed a carbon nanotube atomic force microscope probe. Because the carbon nanotube are well known to have high aspect ratios, small tip radii and high stiffness, carbon nanotube probes have a long lifetime and can be applied for the observation deep trenches. Carbon nanotubes were synthesized by a well-controlled DC arc discharge method, because this method can make nanotubes to have straight shape and high crystalline. The nanotubes were aligned on the knife-edge using an alternating current electrophoresis technique. A commercially available Si probe was used for the base of the nanotube probe. The nanotube probe was fabricated by the SEM manipulation method. The nanotube was then attached tightly to the Si probe by deposition of amorphous carbon. We demonstrate the measurement of a fine pith grating that has vertical walls. However, a carbon nanotube has a problem that is called "Sticking". The sticking is a chatter image on vertical like region in a sample. We solved this problem by applying 2 methods, 1. a large cantilever vibration amplitude in tapping mode, 2. an attractive mode measurement. We demonstrate the non-sticking images by these methods.

  15. Texturing Carbon-carbon Composite Radiator Surfaces Utilizing Atomic Oxygen

    Science.gov (United States)

    Raack, Taylor

    2004-01-01

    Future space nuclear power systems will require radiator technology to dissipate excess heat created by a nuclear reactor. Large radiator fins with circulating coolant are in development for this purpose and an investigation of how to make them most efficient is underway. Maximizing the surface area while minimizing the mass of such radiator fins is critical for obtaining the highest efficiency in dissipating heat. Processes to develop surface roughness are under investigation to maximize the effective surface area of a radiator fin. Surface roughness is created through several methods including oxidation and texturing. The effects of atomic oxygen impingement on carbon-carbon surfaces are currently being investigated for texturing a radiator surface. Early studies of atomic oxygen impingement in low Earth orbit indicate significant texturing due to ram atomic oxygen. The surface morphology of the affected surfaces shows many microscopic cones and valleys which have been experimentally shown to increase radiation emittance. Further study of this morphology proceeded in the Long Duration Exposure Facility (LDEF). Atomic oxygen experiments on the LDEF successfully duplicated the results obtained from materials in spaceflight by subjecting samples to 4.5 eV atomic oxygen from a fixed ram angle. These experiments replicated the conical valley morphology that was seen on samples subjected to low Earth orbit.

  16. International Atomic Energy Agency activities in decommissioning

    International Nuclear Information System (INIS)

    Full text: The International Atomic Energy Agency (IAEA) has been addressing the safety and technical issues of decommissioning for over 20 years, but their focus has been primarily on planning. Up to know, the activities have been on an ad hoc basis and sometimes, important issues have been missed. A new Action Plan on the Decommissioning of Nuclear Facilities has recently been approved by the Agency's board of Governors which will focus the Agency's efforts and ensure that our Member States' concerns are addressed. The new initiatives associated with this Action Plan will help ensure that decommissioning activities in the future are performed in a safe and coherent manner. The International Atomic Energy Agency (IAEA) has been preparing safety and technical documents concerning decommissioning since the mid-1980's. There have been over 30 documents prepared that provide safety requirements, guidance and supporting technical information. Many of these documents are over 10 years old and need updating. The main focus in the past has been on planning for decommissioning. During the past five years, a set of Safety Standards have been prepared and issued to provide safety requirements and guidance to Member States. However, decommissioning was never a real priority with the Agency, but was something that had to be addressed. To illustrate this point, the first requirements documents on decommissioning were issued as part of a Safety Requirements [1] on pre-disposal management of radioactive waste. It was felt that decommissioning did not deserve its own document because it was just part of the normal waste management process. The focus was mostly on waste management. The Agency has assisted Member States with the planning process for decommissioning. Most of these activities have been focused on nuclear power plants and research reactors. Now, support for the decommissioning of other types of facilities is being requested. The Agency is currently providing technical

  17. Observations on the Solubility of Skeletal Carbonates in Aqueous Solutions.

    Science.gov (United States)

    Chave, K E; Deffeyes, K S; Weyl, P K; Garrels, R M; Thompson, M E

    1962-07-01

    Carbonate skeletal materials of marine organisms exhibit a wide range of solubilities in aqueous solutions. In most cases, the dissolution of the carbonate mineral is irreversible and therefore the material can have no true equilibrium solubility. Relative solubilities have been measured in distilled water and in sea water. The least soluble mineral appears to be calcite with low magnesium content; the most soluble is calcite containing 20 to 30 percent MgCO(3) in solid solution. Aragonite has an intermediate solubility. PMID:17774123

  18. Optimization of magnetic powdered activated carbon for aqueous Hg(II) removal and magnetic recovery.

    Science.gov (United States)

    Faulconer, Emily K; von Reitzenstein, Natalia V Hoogesteijn; Mazyck, David W

    2012-01-15

    Activated carbon is known to adsorb aqueous Hg(II). MPAC (magnetic powdered activated carbon) has the potential to remove aqueous Hg to less than 0.2 μg/L while being magnetically recoverable. Magnetic recapture allows simple sorbent separation from the waste stream while an isolated waste potentially allows for mercury recycling. MPAC Hg-removal performance is verified by mercury mass balance, calculated by quantifying adsorbed, volatilized, and residual aqueous mercury. The batch reactor contained a sealed mercury-carbon contact chamber with mixing and constant N(2) (g) headspace flow to an oxidizing trap. Mercury adsorption was performed using spiked ultrapure water (100 μg/L Hg). Mercury concentrations were obtained using EPA method 245.1 and cold vapor atomic absorption spectroscopy. MPAC synthesis was optimized for Hg removal and sorbent recovery according to the variables: C:Fe, thermal oxidation temperature and time. The 3:1 C:Fe preserved most of the original sorbent surface area. As indicated by XRD patterns, thermal oxidation reduced the amorphous characteristic of the iron oxides but did not improve sorbent recovery and damaged porosity at higher oxidation temperatures. Therefore, the optimal synthesis variables, 3:1 C:Fe mass ratio without thermal oxidation, which can achieve 92.5% (± 8.3%) sorbent recovery and 96.3% (± 9%) Hg removal. The mass balance has been closed to within approximately ± 15%. PMID:22104766

  19. Cost evaluation of CO2 sequestration by aqueous mineral carbonation

    International Nuclear Information System (INIS)

    A cost evaluation of CO2 sequestration by aqueous mineral carbonation has been made using either wollastonite (CaSiO3) or steel slag as feedstock. First, the process was simulated to determine the properties of the streams as well as the power and heat consumption of the process equipment. Second, a basic design was made for the major process equipment, and total investment costs were estimated with the help of the publicly available literature and a factorial cost estimation method. Finally, the sequestration costs were determined on the basis of the depreciation of investments and variable and fixed operating costs. Estimated costs are 102 and 77 euro/ton CO2 net avoided for wollastonite and steel slag, respectively. For wollastonite, the major costs are associated with the feedstock and the electricity consumption for grinding and compression (54 and 26 euro/ton CO2 avoided, respectively). A sensitivity analysis showed that additional influential parameters in the sequestration costs include the liquid-to-solid ratio in the carbonation reactor and the possible value of the carbonated product. The sequestration costs for steel slag are significantly lower due to the absence of costs for the feedstock. Although various options for potential cost reduction have been identified, CO2 sequestration by current aqueous carbonation processes seems expensive relative to other CO2 storage technologies. The permanent and inherently safe sequestration of CO2 by mineral carbonation may justify higher costs, but further cost reductions are required, particularly in view of (current) prices of CO2 emission rights. Niche applications of mineral carbonation with a solid residue such as steel slag as feedstock and/or a useful carbonated product hold the best prospects for an economically feasible CO2 sequestration process

  20. International bulletin on atomic and molecular data for fusion

    International Nuclear Information System (INIS)

    The International Bulletin on Atomic and Molecular Data for Fusion is prepared by the Atomic and Molecular Data Unit of the International Atomic Energy Agency. It is distributed free of charge by the IAEA to assist in the development of fusion research and technology. In part 1, the Atomic and Molecular Data Information System (AMDIS) is presented. In Part 2, the indexed papers are listed separately for structure and spectra, atomic and molecular collisions and surface interactions. Part 3 contains all the bibliographic data for both the indexed and non-indexed references. Finally, the Author Index (part 4) refers to the bibliographic references contained in part 3

  1. Recombination of atomic oxygen and hydrogen on amorphous carbon

    International Nuclear Information System (INIS)

    Deposit buildup and fuel entrapment due to amorphous carbon are relevant issues in fusion devices with carbon based plasma facing components. Neutral atomic species play a significant role – atomic hydrogen facilitates the formation of amorphous carbon while atomic oxygen could be used to remove carbon deposits. The kinetics of either reaction depends on the density of neutral species, which in turn is influenced by recombination on the vessel walls. In this work, we measured the probability of heterogeneous recombination of atomic hydrogen and oxygen on amorphous carbon deposits. The recombination coefficients were determined by observing density profiles of atomic species in a closed side-arm of a plasma vessel with amorphous carbon deposit-lined walls. Density profiles were measured with fiber optics catalytic probes. The source of atomic species was inductively coupled radiofrequency plasma. The measured recombination coefficient values were of the order of 10−3 for both species

  2. The international atomic energy agency's programme on inertial fusion energy

    International Nuclear Information System (INIS)

    The International Atomic Energy Agency has been promoting international activity and collaboration related to the use of inertial fusion confinement schemes for energy production for many years. Thorough review of inertial fusion research and a detailed analysis of future prospects has been conducted. Inertial Fusion Energy is now approaching the turning point in the long history from physics oriented research to fusion energy oriented development. The programme of the International Atomic Energy Agency reflects, to some extent, this development

  3. Investigation on single carbon atom transporting through the single-walled carbon nanotube by MD simulation

    International Nuclear Information System (INIS)

    The single carbon atom transporting through the single-walled carbon nanotube has been studied by molecular-dynamics (MD) simulation. We got different trajectories of the carbon atom by changing the input parameters. The simulation results indicate that the single carbon atom with low energy can transport through the carbon nanotube under some input conditions and result in different trajectories being straight line or 'rosette' or circular. (authors)

  4. Electrosorption of inorganic salts from aqueous solution using carbon aerogels.

    Science.gov (United States)

    Gabelich, Christopher J; Tran, Tri D; Suffet, I H Mel

    2002-07-01

    Capacitive deionization (CDI) with carbon aerogels has been shown to remove various inorganic species from aqueous solutions, though no studies have shown the electrosorption behavior of multisolute systems in which ions compete for limited surface area. Several experiments were conducted to determine the ion removal capacity and selectivity of carbon aerogel electrodes, using both laboratory and natural waters. Although carbon aerogel electrodes have been treated as electrical double-layer capacitors, this study showed that ion sorption followed a Langmuir isotherm, indicating monolayer adsorption. The sorption capacity of carbon aerogel electrodes was approximately 1.0-2.0 x 10(-4) equiv/g aerogel, with ion selectivity being based on ionic hydrated radius. Monovalent ions (e.g., sodium) with smaller hydrated radii were preferentially removed from solution over multivalent ions (e.g., calcium) on a percent or molar basis. Because of the relatively small average pore size (4-9 nm) of the carbon aerogel material, only 14-42 m2/g aerogel surface area was available for ion sorption. Natural organic matter may foul the aerogel surface and limit CDI effectiveness in treating natural waters. PMID:12144279

  5. Carbon based thirty six atom spheres

    Science.gov (United States)

    Piskoti, Charles R.; Zettl, Alex K.; Cohen, Marvin L.; Cote, Michel; Grossman, Jeffrey C.; Louie, Steven G.

    2005-09-06

    A solid phase or form of carbon is based on fullerenes with thirty six carbon atoms (C.sub.36). The C.sub.36 structure with D.sub.6h symmetry is one of the two most energetically favorable, and is conducive to forming a periodic system. The lowest energy crystal is a highly bonded network of hexagonal planes of C.sub.36 subunits with AB stacking. The C.sub.36 solid is not a purely van der Waals solid, but has covalent-like bonding, leading to a solid with enhanced structural rigidity. The solid C.sub.36 material is made by synthesizing and selecting out C.sub.36 fullerenes in relatively large quantities. A C.sub.36 rich fullerene soot is produced in a helium environment arc discharge chamber by operating at an optimum helium pressure (400 torr). The C.sub.36 is separated from the soot by a two step process. The soot is first treated with a first solvent, e.g. toluene, to remove the higher order fullerenes but leave the C.sub.36. The soot is then treated with a second solvent, e.g. pyridine, which is more polarizable than the first solvent used for the larger fullerenes. The second solvent extracts the C.sub.36 from the soot. Thin films and powders can then be produced from the extracted C.sub.36. Other materials are based on C.sub.36 fullerenes, providing for different properties.

  6. Structurally uniform and atomically precise carbon nanostructures

    Science.gov (United States)

    Segawa, Yasutomo; Ito, Hideto; Itami, Kenichiro

    2016-01-01

    Nanometre-sized carbon materials consisting of benzene units oriented in unique geometric patterns, hereafter named nanocarbons, conduct electricity, absorb and emit light, and exhibit interesting magnetic properties. Spherical fullerene C60, cylindrical carbon nanotubes and sheet-like graphene are representative forms of nanocarbons, and theoretical simulations have predicted several exotic 3D nanocarbon structures. At present, synthetic routes to nanocarbons mainly lead to mixtures of molecules with a range of different structures and properties, which cannot be easily separated or refined into pure forms. Some researchers believe that it is impossible to synthesize these materials in a precise manner. Obtaining ‘pure’ nanocarbons is a great challenge in the field of nanocarbon science, and the construction of structurally uniform nanocarbons, ideally as single molecules, is crucial for the development of functional materials in nanotechnology, electronics, optics and biomedical applications. This Review highlights the organic chemistry approach — more specifically, bottom-up construction with atomic precision — that is currently the most promising strategy towards this end.

  7. Electrochemical Properties of Nanoporous Carbon Material in Aqueous Electrolytes.

    Science.gov (United States)

    Rachiy, Bogdan I; Budzulyak, Ivan M; Vashchynsky, Vitalii M; Ivanichok, Nataliia Ya; Nykoliuk, Marian O

    2016-12-01

    The paper is devoted to the study of the behavior of capacitor type electrochemical system in the К(+)-containing aqueous electrolytes. Nanoporous carbon material (NCM) was used as the electrode material, obtained by carbonization of plant raw materials with the following chemical activation. Optimization of pore size distribution was carried out by chemical-thermal method using potassium hydroxide as activator. It is shown that obtained materials have high values of capacitance which is realized by charge storage on the electrical double layer and by pseudocapacitive ion storage on the surface of the material. It is established that based on NCM, electrochemical capacitors are stable in all range of current density and material capacity essentially depends on appropriate choice of electrolyte. PMID:26759354

  8. Hydrogen-Atom Attack on Methyl Viologen in Aqueous Solution Studied by Pulse Radiolysis

    DEFF Research Database (Denmark)

    Solar, S.; Solar, W.; Getoff, N.;

    1984-01-01

    Using hydrogen at high pressures of up to 150 bar (0.12 mol dm–3 H2) as an OH scavenger in aqueous MV2+ solutions (pH 1) it is possible to differentiate between two kinds of transient formed simultaneously by H-atom attack on methyl viologen. One of them is assigned to an H adduct on the N atom, ......–7); its absorption spectrum does not change in this pH range....

  9. Chains of carbon atoms: A vision or a new nanomaterial?

    Directory of Open Access Journals (Sweden)

    Florian Banhart

    2015-02-01

    Full Text Available Linear strings of sp1-hybridized carbon atoms are considered as a possible phase of carbon since decades. Whereas the debate about the stability of the corresponding bulk phase carbyne continues until today, the existence of isolated chains of carbon atoms has meanwhile been corroborated experimentally. Since graphene, as the two-dimensional sp2-bonded allotrope of carbon, has become a vast field, the question about the importance of one-dimensional carbon became of renewed interest. The present article gives an overview of the work that has been carried out on chains of carbon atoms in the past one or two decades. The review concentrates on isolated chains of carbon atoms and summarizes the experimental observations to date. While the experimental information is still very limited, many calculations of the physical and chemical properties have been published in the past years. Some of the most important theoretical studies and their importance in the present experimental situation are reviewed.

  10. International nuclear low and atomic energy

    International Nuclear Information System (INIS)

    The aim of this work is to put points on the codification of international law of nuclear energy and its uses in military and peaceful in the first part. The second part was devoted for the imperfection of the law of international nuclear.

  11. Selected specific rates of reactions of transients from water in aqueous solution. II. Hydrogen atom

    International Nuclear Information System (INIS)

    Rates of reactions of hydrogen atoms (from radiolysis of water and other sources) with organic and inorganic molecules, ions, and transients in aqueous solution were tabulated. Directly measured rates obtained by kinetic spectroscopy or conductimetric methods, and relative rates determined by competition kinetics are included. (U.S.)

  12. OCEAN CARBON SINKS AND INTERNATIONAL CLIMATE POLICY

    OpenAIRE

    Katrin Rehdanz; Richard S.J. Tol; Patrick Wetzel

    2005-01-01

    Terrestrial sinks have entered the Kyoto Protocol as offsets for carbon sequestration, but ocean sinks have escaped attention. Ocean sinks are as unexplored and uncertain as were the terrestrial sinks at the time of negotiation. It is not unlikely that certain countries will advocate the inclusion of ocean carbon sinks to reduce their emission reduction obligations. We use a simple model of the international market for carbon dioxide emissions to evaluate who would gain or loose from allowing...

  13. 5. International workshop on autoionization phenomena in atoms. Abstracts

    International Nuclear Information System (INIS)

    Summaries of the reports presented at the 5 International Workshop on Autoionization Phenomena in Atoms (Dubna, 12-14 December 1995). The main topics of these 53 reports are the following ones: photoexcitation of autoionizing states in atoms and ions, autoionization in electron-atom collisions, autoionization in heavy particle collisions, coincidence experiments in autoionization studies, investigations of autoionizing states with lasers and wave functions and decay characteristics of autoionizing states

  14. Excess heat production by the electrolysis of an aqueous potassium carbonate electrolyte and the implications for cold fusion

    International Nuclear Information System (INIS)

    This paper reports that according to a novel atomic model, the predominant source of heat of the phenomenon called cold fusion is the electrocatalytically induced reaction whereby hydrogen atoms undergo transitions to quantized energy levels of lower energy than the conventional ground state. These lower energy states correspond to fractional quantum numbers. The hydrogen electronic transition requires the presence of an energy hole of ∼27.21 eV provided by electrocatalytic reactants (such as Pd2+/Li+, Ti2+, or K+/K+ and results in shrunken atoms analogous to muonic atoms. In the case of deuterium, fusion reactions of shrunken atoms predominantly yielding tritium are possible. Calorimetry of pulsed current and continuous electrolysis of aqueous potassium carbonate (K+/K+ electrocatalytic couple) at a nickel cathode is performed in single-cell dewar calorimetry cells. Excess power out exceeded input power by a factor of >37

  15. Effects of tempering on internal friction of carbon steels

    Energy Technology Data Exchange (ETDEWEB)

    Hoyos, J.J., E-mail: jjhoyos@unal.edu.co [Grupo de Ciencia y Tecnologia de los Materiales, Universidad Nacional de Colombia, Sede Medellin, Carrera 80 Numero 65-223, Medellin (Colombia); Ghilarducci, A.A., E-mail: friccion@cab.cnea.gov.ar [Centro Atomico Bariloche, Comision Nacional de Energia Atomica, Instituto Balseiro-Universidad Nacional de Cuyo, Consejo Nacional de Investigaciones Cientificas y Tecnologicas, Av. Bustillo 9500, 8400 Bariloche RN (Argentina); Salva, H.R., E-mail: salva@cab.cnea.gov.ar [Centro Atomico Bariloche, Comision Nacional de Energia Atomica, Instituto Balseiro-Universidad Nacional de Cuyo, Consejo Nacional de Investigaciones Cientificas y Tecnologicas, Av. Bustillo 9500, 8400 Bariloche RN (Argentina); Chaves, C.A., E-mail: cachaves@unal.edu.co [Grupo de Ciencia y Tecnologia de los Materiales, Universidad Nacional de Colombia, Sede Medellin, Carrera 80 Numero 65-223, Medellin (Colombia); Velez, J.M., E-mail: jmvelez@unal.edu.co [Grupo de Ciencia y Tecnologia de los Materiales, Universidad Nacional de Colombia, Sede Medellin, Carrera 80 Numero 65-223, Medellin (Colombia)

    2011-04-15

    Research highlights: {yields} Time tempering dependent microstructure of two steels is studied by internal friction. {yields} Internal friction indicates the interactions of dislocations with carbon and carbides. {yields} Internal friction detects the first stage of tempering. {yields} Precipitation hardening is detected by the decrease in the background. - Abstract: Two steels containing 0.626 and 0.71 wt.% carbon have been studied to determine the effects of tempering on the microstructure and the internal friction. The steels were annealed at 1093 K, quenched into water and tempered for 60 min at 423 K, 573 K and 723 K. The increase of the tempering time diminishes the martensite tetragonality due to the redistribution of carbon atoms from octahedrical interstitial sites to dislocations. Internal friction spectrum is decomposed into five peaks and an exponential background, which are attributed to the carbide precipitation and the dislocation relaxation process. Simultaneous presence of peaks P1 and P2 indicates the interaction of dislocations with the segregated carbon and carbide precipitate.

  16. Effects of tempering on internal friction of carbon steels

    International Nuclear Information System (INIS)

    Research highlights: → Time tempering dependent microstructure of two steels is studied by internal friction. → Internal friction indicates the interactions of dislocations with carbon and carbides. → Internal friction detects the first stage of tempering. → Precipitation hardening is detected by the decrease in the background. - Abstract: Two steels containing 0.626 and 0.71 wt.% carbon have been studied to determine the effects of tempering on the microstructure and the internal friction. The steels were annealed at 1093 K, quenched into water and tempered for 60 min at 423 K, 573 K and 723 K. The increase of the tempering time diminishes the martensite tetragonality due to the redistribution of carbon atoms from octahedrical interstitial sites to dislocations. Internal friction spectrum is decomposed into five peaks and an exponential background, which are attributed to the carbide precipitation and the dislocation relaxation process. Simultaneous presence of peaks P1 and P2 indicates the interaction of dislocations with the segregated carbon and carbide precipitate.

  17. Nanoscale carbon materials from hydrocarbons pyrolysis: Structure, chemical behavior, utilisation for non-aqueous supercapacitors

    International Nuclear Information System (INIS)

    Highlights: • N-doped and regular carbon nanomaterials were obtained by pyrolitic technique. • Dynamic vapor sorption of different solvents reveals smaller SBET values. • Steric hindrance and specific chemical interactions are the reasons for this. • Nitrogen doping leads to raise of capacitance and coulombic efficiency with non-aqueous N-containing electrolyte. - Abstract: This work systematically studies adsorption properties of carbon nanomaterials that are synthesized through hydrocarbons that is a powerful technique to fabricate different kinds of carbon materials, e.g., nanotubes, nanoshells, onions, including nitrogen substituted. The adsorption properties of the as-synthesized carbons are achieved by low temperature nitrogen adsorption and organic vapors sorption. Heptane, acetonitrile, water, ethanol, benzene and 1-methylimidazole, which are of great importance for development of supercapacitors, are used as substrates. It is discovered that while nitrogen adsorption reveals a high specific surface area, this parameter for most of organic compounds is rather small depending not only on the size of its molecule but also on chemical interactions for a pair adsorbent–adsorbate. The experimental values of heat of adsorption for carbon and N-substituted structures, when Coulomb cross-coupling of nitrogen atoms in adsorbent and adsorbate takes place, confirms this supposition

  18. Nanoscale carbon materials from hydrocarbons pyrolysis: Structure, chemical behavior, utilisation for non-aqueous supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Savilov, Serguei V., E-mail: savilov@chem.msu.ru [Lomonosov Moscow State University, Chemistry Department (Russian Federation); Strokova, Natalia E.; Ivanov, Anton S.; Arkhipova, Ekaterina A. [Lomonosov Moscow State University, Chemistry Department (Russian Federation); Desyatov, Andrey V. [D. Mendeleyev University of Chemical Technology of Russia (Russian Federation); Hui, Xia [Herbert Gleiter Institute of Nanoscience, School of Materials Science and Engineering, Nanjing University of Science and Technology (China); Aldoshin, Serguei M. [Lomonosov Moscow State University, Faculty of Fundamental Physical and Chemical Engineering (Russian Federation); Lunin, Valery V. [Lomonosov Moscow State University, Chemistry Department (Russian Federation)

    2015-09-15

    Highlights: • N-doped and regular carbon nanomaterials were obtained by pyrolitic technique. • Dynamic vapor sorption of different solvents reveals smaller S{sub BET} values. • Steric hindrance and specific chemical interactions are the reasons for this. • Nitrogen doping leads to raise of capacitance and coulombic efficiency with non-aqueous N-containing electrolyte. - Abstract: This work systematically studies adsorption properties of carbon nanomaterials that are synthesized through hydrocarbons that is a powerful technique to fabricate different kinds of carbon materials, e.g., nanotubes, nanoshells, onions, including nitrogen substituted. The adsorption properties of the as-synthesized carbons are achieved by low temperature nitrogen adsorption and organic vapors sorption. Heptane, acetonitrile, water, ethanol, benzene and 1-methylimidazole, which are of great importance for development of supercapacitors, are used as substrates. It is discovered that while nitrogen adsorption reveals a high specific surface area, this parameter for most of organic compounds is rather small depending not only on the size of its molecule but also on chemical interactions for a pair adsorbent–adsorbate. The experimental values of heat of adsorption for carbon and N-substituted structures, when Coulomb cross-coupling of nitrogen atoms in adsorbent and adsorbate takes place, confirms this supposition.

  19. Nitrogenases-A Tale of Carbon Atom(s).

    Science.gov (United States)

    Hu, Yilin; Ribbe, Markus W

    2016-07-11

    Named after its ability to catalyze the reduction of nitrogen to ammonia, nitrogenase has a surprising rapport with carbon-both through the interstitial carbide that resides in the central cavity of its cofactor and through its ability to catalyze the reductive carbon-carbon coupling of small carbon compounds into hydrocarbon products. Recently, a radical-SAM-dependent pathway was revealed for the insertion of carbide, which signifies a novel biosynthetic route to complex bridged metalloclusters. Moreover, a sulfur-displacement mechanism was proposed for the activation of carbon monoxide by nitrogenase, which suggests an essential role of the interstitial carbide in maintaining the stability while permitting a certain flexibility of the cofactor structure during substrate turnover. PMID:27206025

  20. Ternary diffusion of carbon dioxide in alkaline solutions of aqueous sodium hydroxide and aqueous sodium carbonate

    Energy Technology Data Exchange (ETDEWEB)

    Leaist, D.G.

    1985-07-01

    Carbon dioxide dissolved in alkaline solutions diffuses as bicarbonate and carbonate ions produced by the reactions CO/sub 2/+OH/sup -/=HCO/sub 3//sup -/ and CO/sub 2/+2OH/sup -/=CO/sub 3//sup 2 -/+H/sub 2/O. Ternary diffusion coefficients of the systems NaHCO/sub 3/+Na/sub 2/CO/sub 3/+H/sub 2/O and Na/sub 2/CO/sub 3/+NaOH+H/sub 2/O have been measured by a conductimetric technique at 298.15 K. The mixed electrolyte data are transformed by use of the solution equilibria to ternary diffusion coefficients of the systems CO/sub 2/+Na/sub 2/CO/sub 3/+H/sub 2/O and CO/sub 2/+NaOH+H/sub 2/O. Unlike the binary diffusivity of CO/sub 2/ in water (1.9 . 10/sup -9/ m/sup 2/ s/sup -1/), the ternary diffusivity of CO/sub 2/ in alkaline solutions is sensitive to concentration and varies from 0.9 . 10/sup -9/ to 3.5 . 10/sup -9/ m/sup 2/ s/sup -1/ at 298.15 K. Expressions are derived to estimate the transport coefficients of the components from the concentrations and diffusion coefficients of the constituent ions. At high pH values hydroxide-coupled transport leads to rapid diffusion of CO/sub 2/ as CO/sub 3//sup 2 -/. The results are consistent with the Onsager reciprocal relation for isothermal ternary diffusion.

  1. Optimization of magnetic powdered activated carbon for aqueous Hg(II) removal and magnetic recovery

    Energy Technology Data Exchange (ETDEWEB)

    Faulconer, Emily K., E-mail: emily.faulconer@yahoo.com [Department of Environmental Engineering Sciences, University of Florida, 217 Black Hall, P.O. Box 116450, Gainesville, FL 32611-645 (United States); Hoogesteijn von Reitzenstein, Natalia V.; Mazyck, David W. [Department of Environmental Engineering Sciences, University of Florida, 217 Black Hall, P.O. Box 116450, Gainesville, FL 32611-645 (United States)

    2012-01-15

    Highlights: Black-Right-Pointing-Pointer Thermal oxidation of MPAC decreased the amorphous characteristic of iron oxides. Black-Right-Pointing-Pointer Thermal oxidation did not influence magnetic recovery or Hg removal performance. Black-Right-Pointing-Pointer At all thermal oxidation temperatures, the 3:1 MPAC achieved the highest Hg removal. - Abstract: Activated carbon is known to adsorb aqueous Hg(II). MPAC (magnetic powdered activated carbon) has the potential to remove aqueous Hg to less than 0.2 {mu}g/L while being magnetically recoverable. Magnetic recapture allows simple sorbent separation from the waste stream while an isolated waste potentially allows for mercury recycling. MPAC Hg-removal performance is verified by mercury mass balance, calculated by quantifying adsorbed, volatilized, and residual aqueous mercury. The batch reactor contained a sealed mercury-carbon contact chamber with mixing and constant N{sub 2} (g) headspace flow to an oxidizing trap. Mercury adsorption was performed using spiked ultrapure water (100 {mu}g/L Hg). Mercury concentrations were obtained using EPA method 245.1 and cold vapor atomic absorption spectroscopy. MPAC synthesis was optimized for Hg removal and sorbent recovery according to the variables: C:Fe, thermal oxidation temperature and time. The 3:1 C:Fe preserved most of the original sorbent surface area. As indicated by XRD patterns, thermal oxidation reduced the amorphous characteristic of the iron oxides but did not improve sorbent recovery and damaged porosity at higher oxidation temperatures. Therefore, the optimal synthesis variables, 3:1 C:Fe mass ratio without thermal oxidation, which can achieve 92.5% ({+-}8.3%) sorbent recovery and 96.3% ({+-}9%) Hg removal. The mass balance has been closed to within approximately {+-}15%.

  2. Experimental studies on removal of carbon dioxide by aqueous ammonia fine spray

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Experimental studies on carbon dioxide capture in a spray scrubber were carried out.Fine spray of aqueous ammonia was used as CO2 absorbent.Effects of different operating and design parameters on CO2 removal efficiency including concentration of aqueous ammonia,liquid flow rate,total gas flow rate,initial temperature and concentration of carbon dioxide were investigated.

  3. International Atomic Energy Agency: Personal reflections

    International Nuclear Information System (INIS)

    This set of personal recollections reflect a variety of views from twenty-five people who have played major roles in shaping the policies of the IAEA or have made notable contributions to its work at different periods of its history. They provide individual insights - often from a rarely available insider's perspective - into particular aspects of the development of an international organization and thus complement the History of the IAEA written by David Fischer. The articles in this collection illustrate some of the complexities involved in the work of an international organization, where the Governing Bodies consist of over a hundred Member States, with different levels of industrial development, different political outlooks and different interests in the benefits of nuclear energy or concerns about the spread of nuclear weapons

  4. The International Atomic Energy Agency - IAEA

    International Nuclear Information System (INIS)

    The origens, functions and objectives of the IAEA are analysed. The application of safeguards to avoid military uses of nuclear energy is discussed. In the final section the agrement between Brazil and Germany regarding IAEA safeguards, as well as the competence for executing the brazilian program are explained. It is, then, an informative study dealing with nuclear energy and its peaceful path, the creation of International Fuel Cycle Evaluation and nonproliferation

  5. Intergovernmental organisation activities: European Atomic Energy Community, International Atomic Energy Agency, OECD Nuclear Energy Agency

    International Nuclear Information System (INIS)

    European Atomic Energy Community: Proposed legislative instruments, Adopted legislative instruments, Non-legislative instruments, Other activities (meetings). International Atomic Energy Agency: IAEA Action Plan on Nuclear Safety. OECD Nuclear Energy Agency: The Russian Federation to join the OECD Nuclear Energy Agency; Participation by the regulatory authorities of India and the United Arab Emirates in the Multinational Design Evaluation Programme (MDEP); NEA International Workshop on Crisis Communication, 9-10 May 2012; International School of Nuclear Law: 2013; Next NEA International Nuclear Law Essentials Course

  6. Effect of Electrochemical Treatment in Aqueous Ammonium Bicarbonate on Surface Properties of PAN-based Carbon Fibers

    Institute of Scientific and Technical Information of China (English)

    曹海琳; 黄玉东; 张志谦; 孙举涛

    2004-01-01

    The surface properties of PAN-based carbon fibers electrochemically treated in aqueous ammonium bicarbonate before and after treatment were characterized by X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and Dynamic Contact Angle Analysis (DCAA). The results of characterization indicated that the oxygen and nitrogen contents in carbon fiber surface were significantly increased by electrochemical treatment, and amide groups was introduced onto it, which was related with the electrolyte. The AFM photographs illustrated that the roughness of the fiber surface was also increased. The wettibality of the fibers was improved after treatment because the surface energy especially the polar part of it was increased.

  7. Ocean carbon sinks and international climate policy

    International Nuclear Information System (INIS)

    Terrestrial vegetation sinks have entered the Kyoto Protocol as offsets for anthropogenic greenhouse gas emissions, but ocean sinks have escaped attention. Ocean sinks are as unexplored and uncertain as were the terrestrial sinks at the time of negotiation of the Kyoto Protocol. It is not unlikely that certain countries will advocate the inclusion of ocean carbon sinks to reduce their emission reduction obligations in post-2012 negotiations. We use a simple model of the international market for carbon dioxide emissions to evaluate who would gain or loose from allowing for ocean carbon sinks. Our analysis is restricted to information on anthropogenic carbon sequestration within the exclusive economic zone of a country. We use information on the actual carbon flux and derive the human-induced uptake for the period from 1990 onwards. Like the carbon sequestration of business as usual forest management activities, natural ocean carbon sequestration applies at zero costs. The total amount of anthropogenic ocean carbon sequestration is large, also in the exclusive economic zones. As a consequence, it substantially alters the costs of emission reduction for most countries. Countries such as Australia, Denmark, France, Iceland, New Zealand, Norway and Portugal would gain substantially, and a large number of countries would benefit too. Current net exporters of carbon permits, particularly Russia, would gain less and oppose the inclusion of ocean carbon sinks

  8. Ethylbenzene Removal by Carbon Nanotubes from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Bijan Bina

    2012-01-01

    Full Text Available The removal of ethylbenzene (E from aqueous solution by multiwalled, single-walled, and hybrid carbon nanotubes (MWCNTs, SWCNTs, and HCNTs was evaluated for a nanomaterial dose of 1 g/L, concentration of 10–100 mg/L, and pH 7. The equilibrium amount removed by SWCNTs (E: 9.98 mg/g was higher than by MWCNTs and HCNTs. Ethylbenzene has a higher adsorption tendency on CNTs, so that more than 98% of it adsorbed in first 14 min, which is related to the low water solubility and the high molecular weight. The SWCNTs performed better for ethylbenzene sorption than the HCNTs and MWCNTs. Isotherms study indicates that the BET isotherm expression provides the best fit for ethylbenzene sorption by SWCNTs. Carbon nanotubes, specially SWCNTs, are efficient and rapid adsorbents for ethylbenzene which possess good potential applications to maintain high-quality water. Therefore, it could be used for cleaning up environmental pollution to prevent ethylbenzene borne diseases.

  9. International Atomic Energy Agency Annual Report 2014

    International Nuclear Information System (INIS)

    Development Goals. Technical cooperation projects provide expertise in fields where nuclear techniques offer advantages over other approaches, or where they can successfully supplement conventional approaches. The IAEA had 342 million euros in regular budget funding in 2014, while its extrabudgetary expenditures totalled 68.3 million euros. Highlights mentioned in the Annual report include: Nuclear Energy: • The IAEA published several new guidance materials for countries considering to introduce nuclear power programmes. Four new e-learning modules on the IAEA’s ‘Milestones’ approach to nuclear power were launched, bringing to 11 the number of modules in this series available on iaea.org by the end of the year. • More systematic training approaches were used in the nuclear field globally, helping to ensure succession and knowledge management, concluded participants of the International Conference on Human Resource Development for Nuclear Power Programmes. • The International Symposium on Uranium Raw Material for the Nuclear Fuel Cycle highlighted new initiatives such as innovative financing and the use of advanced technologies in 'smart mines', and the need for increased attention to stakeholder engagement. Nuclear Sciences and Applications: • As part of the IAEA’s effort to meet growing Member State needs, the Renovation of the Nuclear Applications Laboratories (ReNuAL) project began on 1 January, 2014. Following completion of the feasibility study in February, the strategic plan for the project was issued in May, and conceptual designs for the new buildings were completed in November. A donor package providing detailed information on the project and its requirements was made available to Member States last December. • Against the background of outbreaks of avian influenza H5N1 and H7N9 and other animal diseases that can spread to humans, the IAEA established the VetLab network of animal diagnostic laboratories in Africa to intensify its work on

  10. Strategies for enhancing the performance of carbon/carbon supercapacitors in aqueous electrolytes

    International Nuclear Information System (INIS)

    Presented paper describes and critically comments major recent strategies for improving electrochemical capacitor performance. Particularly, carbon based electrodes and aqueous electrolytes have been considered. A novel concept of redox active electrolytes as a source of pseudocapacitance effect as well as profits and cons of such system have been discussed. The electrochemical performance of capacitor operating in such electrolyte solution is reported. Furthermore, some advantageous features of bio-inspired system based on bromine-cerium solution acting as oscillator are also presented

  11. Atomic scale simulation of carbon nanotube nucleation from hydrocarbon precursors

    OpenAIRE

    Khalilov, Umedjon; Bogaerts, Annemie; Neyts, Erik C.

    2015-01-01

    Atomic scale simulations of the nucleation and growth of carbon nanotubes is essential for understanding their growth mechanism. In spite of over twenty years of simulation efforts in this area, limited progress has so far been made on addressing the role of the hydrocarbon growth precursor. Here we report on atomic scale simulations of cap nucleation of single-walled carbon nanotubes from hydrocarbon precursors. The presented mechanism emphasizes the important role of hydrogen in the nucleat...

  12. Study of the reaction of carbon with atomic oxygen

    International Nuclear Information System (INIS)

    This research thesis reports the study of reactions of carbon when in contact with atomic oxygen in order to have a better understanding of the combustion mechanism. It appears that, at room temperature, oxygen atoms impacting the carbon surface do not all react with this surface (the reaction shock efficiency is very low). At temperatures higher than 200 C, all atoms which reach the surface react with it and the efficiency is much higher. The study of the reaction rate with respect to temperature allows three domains of reaction conditions to be distinguished according to the stability of formed surface oxides. The initial degassing of carbon results in a temporary excitation of the reaction rate, even with atomic oxygen. Whatever is the temperature, reaction is localised at the vicinity of the sample outer surface (this means that the regime is constantly diffusion). The BET surface of carbons does not vary with the reaction. As texture, the structure of the different carbons does not seem to have an influence on the reaction with atomic oxygen. Even though results are obtained in very different temperature ranges (600 C with O2, less than 200 C with atomic oxygen), there is an analogy between some phenomena noticed with atomic oxygen and molecular oxygen: surface oxides play a prevailing role

  13. Theoretical study of adsorption of lithium atom on carbon nanotube

    OpenAIRE

    Senami, Masato; Ikeda, Yuji; Fukushima, Akinori; Tachibana, Akitomo

    2011-01-01

    We investigate the adsorption of lithium atoms on the surface of the (12,0) single wall carbon nanotube (SWCNT) by using ab initio quantum chemical calculations. The adsorption of one lithium atom on the inside of this SWCNT is favored compared to the outside. We check this feature by charge transfer and regional chemical potential density. The adsorption of multiple lithium atoms on the interior of the SWCNT is studied in terms of adsorption energy and charge transfer. We show that repulsive...

  14. 24. International Conference on Atomic Collisions in Solids ICACS-24

    International Nuclear Information System (INIS)

    This Book contains the abstracts of invited and contributed talks submitted for presentation at the 24th International Conference on Atomic Collisions in Solids - ICACS-24. Out of nearly 200 submitted abstracts the International Programme Committee selected 46 oral and 89 poster contributions. Furthermore, 15 plenary invited lectures and the honorary Lindhard lecture are included in the scientific program. An additional tutorial day with 4 tutorial lectures is organised on Sunday prior to the Conference.

  15. The efficiency of magnetic carbon activated by iron oxide nanoparticles in removing of Cu (II from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Salehe Salehnia

    2016-04-01

    Full Text Available Background and Aim: Copper ions, due to forming complexes with organic and mineral compounds, can have worrying effects on health and environment. In the present study, the effect of powdered magnetic carbon activated by iron-oxide nanoparticles in removing of CU (V; II from aqueous solutions was assessed. Materials and Methods: This experimental study aimed at determining the effect of powdered magnetic carbon activated  by iron-oxide nanoparticles  parameters including PH, contact time, absorbing dose, and initial concentration on copper(II removal .from aqueous solutions; through an indirect current. In order to assess the qualities of the synthetized adsorbent, TGA, FT-IR and SEM tests were applied. Residual concentration of copper was measured at 324nm wavelength by means of atomic absorption spectrometry flame. The obtained data was analyzed using Langmuir and Freundlich isotherm model. Result: It was found that synthetic nanoparticles(PH=10, with the adsorbent dosage of 1gr/l, can remove more than 96% of copper ions from aqueous solutions at 2 minutes. Also, the results showed that copper absorption pattern is more in accord with Langmuir model.  Conclusion: Based on the current findings , magnetic synthesized nanoparticles coated with carbon. are in sporadic form in aqueous solutions. and can easily be separated using external magnetic environment. Moreover, because of existant active carbon sites absorption in iron oxide structure suferficial absorbtion capacity increases and and these nanoparticles reveal to have a high performance in the removing process of copper pollutants from aqueous solutions.

  16. Radiation therapy. 1990-2001. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalog lists all sales publications of the International Atomic Energy Agency dealing with Radiation Therapy, and issued during the period 1 January 1990 - 30 April 2001. Most publications are issued in English, though some are also available in other languages. These are noted in the catalogue

  17. 4th International Conference on Exotic Nuclei and Atomic Masses

    CERN Document Server

    Gross, Carl J; Rykaczewski, Krzysztof P; The European Physical Journal A : Volume 25, Supplement 1, 2005

    2005-01-01

    The International Conference on Exotic Nuclei and Atomic Masses (ENAM) has gained the status of the premier meeting for the physics of nuclei far from stability. The selected and refereed papers presenting the main results constitute valuable proceedings that offer everyone working in this field an authoritative and comprehensive source of reference.

  18. Environment. 1980-1994. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    The catalogue lists all publications of the International Atomic Energy Agency dealing with the Environment issued during the period 1980-1993. The major subjects covered include: effect of agrochemical residues on soils and aquatic ecosystems, application of radioisotopes in conservation of the environment, siting of nuclear power plants, environmental isotope data and environmental contamination due to nuclear accidents

  19. Environment. 1990-2001. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalog lists all sales publications of the International Atomic Energy Agency dealing with the Environment, and issued during the period 1 January 1990 - 30 April 2001. Most publications are issued in English, though some are also available in other languages. These are noted in the catalogue

  20. 4. International symposium. Ural atomic, Ural industrial. Abstracts

    International Nuclear Information System (INIS)

    In the book of abstracts submitted to the 4-th International symposium Ural atomic, Ural industrial held on September 30 - October 3, 1996, in Ekaterinburg, Russia, the publications cover the results of studies on: 1) problems of radioactive contamination of territories; 2) medical implications of radioactive contamination; 3) complex solution of the problems of ecologically adverse territories

  1. Aqueous adsorption and removal of organic contaminants by carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Jin-Gang, E-mail: yujg@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China); Zhao, Xiu-Hui; Yang, Hua [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China); Chen, Xiao-Hong [Collaborative Innovation Center of Resource-conserving and Environment-friendly Society and Ecological Civilization, Changsha, Hunan 410083 (China); Yang, Qiaoqin [Department of Mechanical Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9 (Canada); Yu, Lin-Yan [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China); Jiang, Jian-Hui [College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082 (China); Chen, Xiao-Qing, E-mail: xqchen@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China)

    2014-06-01

    Organic contaminants have become one of the most serious environmental problems, and the removal of organic contaminants (e.g., dyes, pesticides, and pharmaceuticals/drugs) and common industrial organic wastes (e.g., phenols and aromatic amines) from aqueous solutions is of special concern because they are recalcitrant and persistent in the environment. In recent years, carbon nanotubes (CNTs) have been gradually applied to the removal of organic contaminants from wastewater through adsorption processes. This paper reviews recent progress (145 studies published from 2010 to 2013) in the application of CNTs and their composites for the removal of toxic organic pollutants from contaminated water. The paper discusses removal efficiencies and adsorption mechanisms as well as thermodynamics and reaction kinetics. CNTs are predicted to have considerable prospects for wider application to wastewater treatment in the future. - Highlights: • We summarize the most recent research progress of CNTs for removal of organics. • Adsorption mechanisms between CNTs and organics were elucidated in detail. • The developing trends and prospects of CNTs for removal of organics were discussed.

  2. Aqueous adsorption and removal of organic contaminants by carbon nanotubes

    International Nuclear Information System (INIS)

    Organic contaminants have become one of the most serious environmental problems, and the removal of organic contaminants (e.g., dyes, pesticides, and pharmaceuticals/drugs) and common industrial organic wastes (e.g., phenols and aromatic amines) from aqueous solutions is of special concern because they are recalcitrant and persistent in the environment. In recent years, carbon nanotubes (CNTs) have been gradually applied to the removal of organic contaminants from wastewater through adsorption processes. This paper reviews recent progress (145 studies published from 2010 to 2013) in the application of CNTs and their composites for the removal of toxic organic pollutants from contaminated water. The paper discusses removal efficiencies and adsorption mechanisms as well as thermodynamics and reaction kinetics. CNTs are predicted to have considerable prospects for wider application to wastewater treatment in the future. - Highlights: • We summarize the most recent research progress of CNTs for removal of organics. • Adsorption mechanisms between CNTs and organics were elucidated in detail. • The developing trends and prospects of CNTs for removal of organics were discussed

  3. Atomic scale simulation of carbon nanotube nucleation from hydrocarbon precursors

    Science.gov (United States)

    Khalilov, Umedjon; Bogaerts, Annemie; Neyts, Erik C.

    2015-12-01

    Atomic scale simulations of the nucleation and growth of carbon nanotubes is essential for understanding their growth mechanism. In spite of over twenty years of simulation efforts in this area, limited progress has so far been made on addressing the role of the hydrocarbon growth precursor. Here we report on atomic scale simulations of cap nucleation of single-walled carbon nanotubes from hydrocarbon precursors. The presented mechanism emphasizes the important role of hydrogen in the nucleation process, and is discussed in relation to previously presented mechanisms. In particular, the role of hydrogen in the appearance of unstable carbon structures during in situ experimental observations as well as the initial stage of multi-walled carbon nanotube growth is discussed. The results are in good agreement with available experimental and quantum-mechanical results, and provide a basic understanding of the incubation and nucleation stages of hydrocarbon-based CNT growth at the atomic level.

  4. International human cooperation in Japan Atomic Energy Research Institute

    International Nuclear Information System (INIS)

    Rearing of talented persons in the area of nuclear energy is one of the important works in Japan Atomic Energy Research Institute. In this report, the present situations and future schedules of international human cooperation in this area wsere summarized. First, the recent activities of International Nuclear Technology Center were outlined in respect of international human cooperation. A study and training course which was started in cooperation with JICA and IAEA from the middle of eighties and the international nuclear safety seminar aiming at advancing the nuclear safety level of the world are now being put into practice. In addition, a study and training for rearing talented persons was started from 1996 to improve the nuclear safety level of the neighbouring countries. The activities of the nuclear research interchange system by Science and Technology Agency established in 1985 and Bilateral Co-operation Agreement from 1984 were explained and also various difficulties in the international cooperation were pointed out. (M.N.)

  5. Aqueous solutions of acidic ionic liquids for enhanced stability of polyoxometalate-carbon supercapacitor electrodes

    Science.gov (United States)

    Hu, Chenchen; Zhao, Enbo; Nitta, Naoki; Magasinski, Alexandre; Berdichevsky, Gene; Yushin, Gleb

    2016-09-01

    Nanocomposites based on polyoxometalates (POMs) nanoconfined in microporous carbons have been synthesized and used as electrodes for supercapacitors. The addition of the pseudocapacitance from highly reversible redox reaction of POMs to the electric double-layer capacitance of carbon lead to an increase in specific capacitance of ∼90% at 1 mV s-1. However, high solubility of POM in traditional aqueous electrolytes leads to rapid capacity fading. Here we demonstrate that the use of aqueous solutions of protic ionic liquids (P-IL) as electrolyte instead of aqueous sulfuric acid solutions offers an opportunity to significantly improve POM cycling stability. Virtually no degradation in capacitance was observed in POM-based positive electrode after 10,000 cycles in an asymmetric capacitor with P-IL aqueous electrolyte. As such, POM-based carbon composites may now present a viable solution for enhancing energy density of electrical double layer capacitors (EDLC) based on pure carbon electrodes.

  6. A Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation

    DEFF Research Database (Denmark)

    Bonalumi, Davide; Valenti, Gianluca; Lillia, Stefano;

    2016-01-01

    Post-combustion carbon capture technologies seem to be necessary to realize the CO2 mitigation policies internationally shared for the next future, despite none of them appears to be ready for full-scale applications. This work considers the aqueous ammonia based process for a coal-fired Ultra...... Super Critical power plant. Two layouts are simulated with Aspen Plus employing the recently recalibrated Extended UNIQUAC thermodynamic model. The first one operates at chilling conditions, which yield to salt precipitation, and is taken as reference because already analyzed in previous studies......, a lower SPECCA of 2.58 MJ/kgco2. The latter layout is a better choice also from the perspective of the plant operation since it does not present the salt precipitation....

  7. A synthesis of carbon in international trade

    Directory of Open Access Journals (Sweden)

    G. P. Peters

    2012-08-01

    Full Text Available In a globalised world, the transfer of carbon between regions, either physically or embodied in production, represents a substantial fraction of global carbon emissions. The resulting emission transfers are important for balancing regional carbon budgets and for understanding the drivers of emissions. In this paper we synthesise current understanding in two parts: (1 CO2 emissions embodied in goods and services that are produced in one country but consumed in others, and (2 carbon physically present in fossil fuels, petroleum-derived products, harvested wood products, crops, and livestock products. We describe the key differences between studies and provide a consistent set of estimates using the same definitions, modelling framework, and consistent data. We find the largest trade flows of carbon in international trade in 2004 were fossil fuels (2673 MtC, 37 % of global emissions, CO2 embodied in traded goods and services (1661 MtC, 22 % of global emissions, crops (522 MtC, 31 % of total harvested crop carbon, petroleum-based products (183 MtC, 50 % of their total production, harvested wood products (149 MtC, 40 % of total roundwood extraction, and livestock products (28 MtC, 22 % of total livestock carbon. We find that for embodied CO2 emissions, estimates from independent studies are robust, and that differences between individual studies are not a reflection of the uncertainty in consumption-based estimates, but rather these differences result from the use of different production-based emissions input data and different definitions for allocating emissions to international trade. After adjusting for these issues, results across independent studies converge to give less uncertainty than previously assumed. For physical carbon flows there are relatively few studies to be synthesised, but differences between existing studies are due to the method of allocating to international trade, with some studies using

  8. A synthesis of carbon in international trade

    Directory of Open Access Journals (Sweden)

    G. P. Peters

    2012-03-01

    Full Text Available In a globalised world, the transfer of carbon between regions, either physically or embodied in production, represents a substantial fraction of global carbon emissions. The resulting emission transfers are important for balancing regional carbon budgets and for understanding the drivers of regional emissions. In this paper we synthesise current understanding in two parts: (1 embodied CO2 emissions from the production of goods and services produced in one country but consumed in others, (2 physical carbon flows in fossil fuels, petroleum-derived products, harvested wood products, crops, and livestock. We describe the key differences between studies and provide a consistent set of estimates using the same definitions, modelling framework, and consistent data. We find the largest trade flows of carbon in international trade in 2004 were fossil fuels (2673 MtC, 37% of global emissions, CO2 embodied in traded goods and services (1661 MtC, 22% of global emissions, livestock (651 MtC, 20% of total livestock carbon, crops (522 MtC, 31% of total harvested crop carbon, petroleum-based products (183 MtC, 50% of their total production, and harvested wood products (149 MtC, 40% of total roundwood extraction. We find that for embodied CO2 emissions estimates from independent studies are robust. We found that differences between individual studies is not representative of the uncertainty in consumption-based estimates as different studies use different production-based emission estimates as input and different definitions of allocating emissions to international trade. After adjusting for these issues, results across independent studies converge to give less uncertainty than previously assumed. For physical carbon flows there are relatively few studies to be synthesised, but differences between existing studies are due to the method of allocating to international trade with some studies using "apparent consumption" as opposed

  9. A synthesis of carbon in international trade

    Science.gov (United States)

    Peters, G. P.; Davis, S. J.; Andrew, R.

    2012-08-01

    In a globalised world, the transfer of carbon between regions, either physically or embodied in production, represents a substantial fraction of global carbon emissions. The resulting emission transfers are important for balancing regional carbon budgets and for understanding the drivers of emissions. In this paper we synthesise current understanding in two parts: (1) CO2 emissions embodied in goods and services that are produced in one country but consumed in others, and (2) carbon physically present in fossil fuels, petroleum-derived products, harvested wood products, crops, and livestock products. We describe the key differences between studies and provide a consistent set of estimates using the same definitions, modelling framework, and consistent data. We find the largest trade flows of carbon in international trade in 2004 were fossil fuels (2673 MtC, 37 % of global emissions), CO2 embodied in traded goods and services (1661 MtC, 22 % of global emissions), crops (522 MtC, 31 % of total harvested crop carbon), petroleum-based products (183 MtC, 50 % of their total production), harvested wood products (149 MtC, 40 % of total roundwood extraction), and livestock products (28 MtC, 22 % of total livestock carbon). We find that for embodied CO2 emissions, estimates from independent studies are robust, and that differences between individual studies are not a reflection of the uncertainty in consumption-based estimates, but rather these differences result from the use of different production-based emissions input data and different definitions for allocating emissions to international trade. After adjusting for these issues, results across independent studies converge to give less uncertainty than previously assumed. For physical carbon flows there are relatively few studies to be synthesised, but differences between existing studies are due to the method of allocating to international trade, with some studies using "apparent consumption" as opposed to "final

  10. Proceedings of the international seminar on atomic processes in plasmas

    Energy Technology Data Exchange (ETDEWEB)

    Kato, Takako; Murakami, Izumi [eds.

    2000-01-01

    The International Seminar on Atomic Processes in Plasmas (ISAPP), a satellite meeting to the ICPEAC was held July 28-29 at the National Institute for Fusion Science in Toki, Gifu, Japan. About 110 scientists attended the ISAPP meeting and discussed atomic processes and atomic data required for fusion research. This Proceedings book includes the papers of the talks, posters and panel discussion given at the meeting. The invited talks described the super configuration array method for complex spectra, near-LTE atomic kinetics, R-matrix calculations, the binary-encounter dipole model for electron-impact ionization of molecules, other calculations of molecular processes, the ADAS project and the NIFS atomic data-base, and a survey of the role of molecular processes in divertor plasmas. On the experimental side crossed-beam ion-ion collision-experiments for charge transfer, and storage-ring and EBIT measurements of ionization, excitation and dielectronic recombination cross-sections were presented, and atomic processes important for x-ray laser experiments and x-ray spectroscopy of astrophysical plasmas were described. The new method of plasma polarization spectroscopy was outlined. There was also a spectroscopic study of particle transport in JT-60U, new results for detached plasmas, and a sketch of the first hot plasma experiments with the Large Helical Device recently completed at NIFS. The 63 of the presented papers are indexed individually. (J.P.N.)

  11. Proceedings of the international seminar on atomic processes in plasmas

    International Nuclear Information System (INIS)

    The International Seminar on Atomic Processes in Plasmas (ISAPP), a satellite meeting to the ICPEAC was held July 28-29 at the National Institute for Fusion Science in Toki, Gifu, Japan. About 110 scientists attended the ISAPP meeting and discussed atomic processes and atomic data required for fusion research. This Proceedings book includes the papers of the talks, posters and panel discussion given at the meeting. The invited talks described the super configuration array method for complex spectra, near-LTE atomic kinetics, R-matrix calculations, the binary-encounter dipole model for electron-impact ionization of molecules, other calculations of molecular processes, the ADAS project and the NIFS atomic data-base, and a survey of the role of molecular processes in divertor plasmas. On the experimental side crossed-beam ion-ion collision-experiments for charge transfer, and storage-ring and EBIT measurements of ionization, excitation and dielectronic recombination cross-sections were presented, and atomic processes important for x-ray laser experiments and x-ray spectroscopy of astrophysical plasmas were described. The new method of plasma polarization spectroscopy was outlined. There was also a spectroscopic study of particle transport in JT-60U, new results for detached plasmas, and a sketch of the first hot plasma experiments with the Large Helical Device recently completed at NIFS. The 63 of the presented papers are indexed individually. (J.P.N.)

  12. Dependence of internal conversion coefficient on atom state

    International Nuclear Information System (INIS)

    Calculations of the internal conversion coefficient (ICC) for the (Fe) atom d-shell containing 6 electrons at a maximum occupation number of 10 are presented. In the relativistic approach use is made of the multiconfiguration approximation, which makes it possible to take account of the intermediate coupling in nonfilled shells. The energy matrix has been calculated in the determinantal basis of these configurations and then diagonalized. Radial single-electron wave functions have been calculated by the relativistic method of the Hartry-Fock-Dirac self consistent field. Occupational numbers of Fe d-subshells for the 5D basic multiplet states are given. Atom electrical and magnetic ICC are analyzed. Electrical ICC are practically the same for all the levels. The electrical ICC calculated for one electron does not depend on the spin orientation. Magnetic ICC show considerable dependence of the atom state. Within the multiplet limits the ICC change smoothly, decreasing for higher levels

  13. Reactions of carbon atoms in pulsed molecular beams

    Energy Technology Data Exchange (ETDEWEB)

    Reisler, H. [Univ. of Southern California, Los Angeles (United States)

    1993-12-01

    This research program consists of a broad scope of experiments designed to unravel the chemistry of atomic carbon in its two spin states, P and D, by using well-controlled initial conditions and state-resolved detection of products. Prerequisite to the proposed studies (and the reason why so little is known about carbon atom reactions), is the development of clean sources of carbon atoms. Therefore, in parallel with the studies of its chemistry and reaction dynamics, the authors continuously explore new, state-specific and efficient ways of producing atomic carbon. In the current program, C({sup 3}P) is produced via laser ablation of graphite, and three areas of study are being pursued: (i) exothermic reactions with small inorganic molecules (e.g., O{sub 2}, N{sub 2}O, NO{sub 2}) that can proceed via multiple pathways; (ii) the influence of vibrational and translational energy on endothermic reactions involving H-containing reactants that yield CH products (e.g., H{sub 2}O H{sub 2}CO); (iii) reactions of C({sup 3}P) with free radicals (e.g., HCO, CH{sub 3}O). In addition, the authors plan to develop a source of C({sup 1}D) atoms by exploiting the pyrolysis of diazotetrazole and its salts in the ablation source. Another important goal involves collaboration with theoreticians in order to obtain relevant potential energy surfaces, rationalize the experimental results and predict the roles of translational and vibrational energies.

  14. Environment, 1986-1997. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with Environment and issued during the period of 1986-1997. Some earlier titles which form part of an established series or are still considered of importance have been included. Most publications are in English. Proceedings of conferences, symposia and panels of experts may contain papers in languages other than English, but all of these papers have abstracts in English

  15. Earth sciences. 1990-2001. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with Earth Sciences and issued during the period 1 January 1990 - 31 May 2001. Most publications are issued in English, though some are also available in other languages. This is noted as A for Arabic, C for Chinese, E for English, F for French, R for Russian and S for Spanish before the relevant ISBN number

  16. Covalent bond orders for non-bonded atoms: The case for carbon-carbon interactions

    International Nuclear Information System (INIS)

    The Cioslowski-Mixon (CM) covalent bond order and the atoms-in-molecules (AIM) delocalization index can be used to study bonding characteristics between atoms not bonded in the conventional chemical sense. In particular, the bond orders between atoms (AIM basins) with one intervening atom evolve in a predictable manner and are related to the bond orders of conventionally bonded species. The CM approach shows that it is the tails of the incompletely localized orbitals that provide for such interactions. Single, multiple, and resonant bond effects are seen which are physically meaningful and useful as an additional characterization of molecular bonding. The important case of carbon-carbon interactions is studied here.

  17. Neutral Atomic Carbon in Centers of Galaxies

    OpenAIRE

    Israel, F.P.; Baas, F

    2001-01-01

    We present measurements of the emission from the centers of fifteen spiral galaxies in the 3P1-3P0 [CI] fine-structure transition at 492 GHz. Observed galaxy centers range from quiescent to starburst to active. The intensities of neutral carbon, the J=2-1 transition of 13CO and the J=4-3 transition of 12CO are compared in matched beams. Most galaxy centers emit more strongly in [CI] than in 13CO, completely unlike the situation pertaining to Galactic molecular cloud regions. [CI] intensities ...

  18. Neutral atomic carbon in dense molecular clouds

    Science.gov (United States)

    Zmuidzinas, J.; Betz, A. L.; Boreiko, R. T.; Goldhaber, D. M.

    1988-01-01

    The 370 micron 3P2-3P1 fine-structure line of neutral carbon was detected in seven sources: OMC 1, NGC 2024, S140, W3, DR 21, M17, and W51. Simultaneous analysis of J = 2-1 data and available observations of the J = 1-0 line make it possible to deduce optical depths and excitation temperatures for these lines. These data indicate that both C I lines are likely to be optically thin, and that the ratio of C I to CO column densities in these clouds is typically about 0.1.

  19. Macroeconomic modelling of international carbon tax regimes

    International Nuclear Information System (INIS)

    An econometric model of fossil fuel demand has been estimated for eight OECD countries, relating coal, oil and gas demands to GDP and prices. In addition, for five of these countries, a model of endogenous technical progress has been estimated, representing the decline in energy intensity as a function of price and macroeconomic variables. This aims to include both price induced innovation in energy and structural change in the economy as long term determinants of energy consumption. A number of possible international carbon/energy tax agreements are simulated, showing the impacts on carbon dioxide emissions and comparing the two models. It is shown that the endogenous technical change model does include an important element that is missed in the more conventional approach. However in the long run the magnitude of taxes required to stabilise or reduce emissions would be large, and it is suggested that other non-price policies will become more important. (Author)

  20. Comparison of two electrolyte models for the carbon capture with aqueous ammonia

    DEFF Research Database (Denmark)

    Darde, Victor; Thomsen, Kaj; van Well, Willy J.M.;

    2012-01-01

    Post-combustion carbon capture is attracting much attention due to the fact that it can be retrofitted on existing coal power plants. Among the most interesting technologies is the one that employs aqueous ammonia solutions to absorb the generated carbon dioxide. The evaluation of such process...

  1. First principles investigation of interaction between impurity atom (Si, Ge, Sn) and carbon atom in diamond-like carbon system

    International Nuclear Information System (INIS)

    The interaction between impurity atom (Si, Ge, and Sn) and carbon atom in diamond-like carbon (DLC) system was investigated by the first principles simulation method based on the density functional theory. The tetrahedral configuration was selected as the calculation model for simplicity. When the bond angle varied in a range of 90°–130° from the equivalent state of 109.471°, the distortion energy and the electronic structures including charge density of the highest occupied molecular orbital (HOMO) and partial density of state (PDOS) in the different systems were calculated. The results showed that the addition of Si, Ge and Sn atom into amorphous carbon matrix significantly decreased the distortion energy of the system as the bond angles deviated from the equilibrium one. Further studies of the HOMO and PDOS indicated that the weak covalent bond between Si(Ge, Sn) and C atoms was formed with the decreased strength and directionality, which were influenced by the electronegative difference. These results implied that the electron transfer behavior at the junction of carbon nano-devices could be tailored by the impurity element, and the compressive stress in DLC films could be reduced by the incorporation of Si, Ge and Sn because of the formation of weaker covalent bonds. - Highlights: ►Distortion energy after bond angle distortion was decreased comparing with C-C unit. ►The weak covalent bond was formed between impurity atoms and corner carbon atoms. ►Observed electron transfer behavior affected the strength and directionality of bond. ►Reduction of strength and directionality of bond contributed to small energy change.

  2. Direct experimental determination of the atomic structure at internal interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Browning, N.D. [Oak Ridge National Lab., TN (United States)]|[Illinois Univ., Chicago, IL (United States); Pennycook, S.J. [Oak Ridge National Lab., TN (United States)

    1995-07-01

    A crucial first step in understanding the effect that internal interfaces have on the properties of materials is the ability to determine the atomic structure at the interface. As interfaces can contain atomic disorder, dislocations, segregated impurities and interphases, sensitivity to all of these features is essential for complete experimental characterization. By combining Z-contrast imaging and electron energy loss spectroscopy (EELS) in a dedicated scanning transmission electron microscope (STEM), the ability to probe the structure, bonding and composition at interfaces with the necessary atomic resolution has been obtained. Experimental conditions can be controlled to provide, simultaneously, both incoherent imaging and spectroscopy. This enables interface structures observed in the image to be interpreted intuitively and the bonding in a specified atomic column to be probed directly by EELS. The bonding and structure information can then be correlated using bond-valence sum analysis to produce structural models. This technique is demonstrated for 25{degrees}, 36{degrees} and 67{degrees} symmetric and 45{degrees} and 25{degrees} asymmetric [001] tilt grain boundaries in SrTiO{sub 3} The structures of both types of boundary were found to contain partially occupied columns in the boundary plane. From these experimental results, a series of structural units were identified which could be combined, using continuity of gain boundary structure principles, to construct all [001] tilt boundaries in SrTiO{sub 3}. Using these models, the ability of this technique to address the issues of vacancies and dopant segregation at grain boundaries in electroceramics is discussed.

  3. Alternate Funding Sources for the International Atomic Energy Agency

    Energy Technology Data Exchange (ETDEWEB)

    Toomey, Christopher; Wyse, Evan T.; Kurzrok, Andrew J.; Swarthout, Jordan M.

    2012-09-04

    Since 1957, the International Atomic Energy Agency (IAEA) has worked to ensure the safe and responsible promotion of nuclear technology throughout the world. The IAEA operates at the intersection of the Nuclear Nonproliferation Treaty’s (NPT) fourth and third articles, which guarantee Parties to the Treaty the right to peaceful uses of nuclear technology, provided those activities are placed under safeguards verified by the IAEA. However, while the IAEA has enjoyed substantial success and prestige in the international community, there is a concern that its resources are being stretched to a point where it may no longer be possible to execute its multifaceted mission in its entirety. As noted by the Director General (DG) in 2008, demographics suggest that every aspect of the IAEA’s operations will be in higher demand due to increasing reliance on non-carbon-based energy and the concomitant nonproliferation, safety, and security risks that growth entails. In addition to these nuclear energy concerns, the demand for technical developmental assistance in the fields of food security, resource conservation, and human health is also predicted to increase as the rest of the world develops. Even with a 100% value-for-money rating by the U.S. Office of Management and Budget (OMB) and being described as an “extraordinary bargain” by the United Nations Secretary-General’s High-level Panel on Threats, Challenges and Change, real budget growth at the Agency has been limited to zero-real growth for a better part of the last two decades. Although the 2012 regular budget (RB) received a small increase for most programs, the 2013 RB has been set at zero-real growth. As a result, the IAEA has had to defer infrastructure investments, which has hindered its ability to provide the public goods its Members seek, decreased global security and development opportunities, and functionally transformed the IAEA into a charity, dependent on extrabudgetary (EB) contributions to sustain

  4. Arsenic(III) adsorption from aqueous solutions on novel carbon cryogel/ceria nanocomposite

    OpenAIRE

    Tamara Minović Arsić; Ana Kalijadis; Branko Matović; Milovan Stoiljković; Jelena Pantić; Jovan Jovanović; Rada Petrović; Bojan Jokić; Biljana Babić

    2016-01-01

    Carbon cryogel/ceria composite, with 10 wt.% of ceria, was synthesized by mixing of ceria and carbon cryogel (CC). The sample was characterized by field emission scanning electron microscopy, nitrogen adsorption and X-ray diffraction. The adsorption of arsenic(III) ions from aqueous solutions on carbon cryogel/ceria nanocomposite was studied as a function of time, solution pH and As(III) ion concentration. The results are correlated with previous investigations of adsorption mechanism of arse...

  5. Mechanisms of aqueous wollastonite carbonation as a possible CO2 sequestration process

    International Nuclear Information System (INIS)

    The mechanisms of aqueous wollastonite carbonation as a possible carbon dioxide sequestration process were investigated experimentally by systematic variation of the reaction temperature, CO2 pressure, particle size, reaction time, liquid to solid ratio and agitation power. The carbonation reaction was observed to occur via the aqueous phase in two steps: (1) Ca leaching from the CaSiO3 matrix and (2) CaCO3 nucleation and growth. Leaching is hindered by a Ca-depleted silicate rim resulting from incongruent Ca-dissolution. Two temperature regimes were identified in the overall carbonation process. At temperatures below an optimum reaction temperature, the overall reaction rate is probably limited by the leaching rate of Ca. At higher temperatures, nucleation and growth of calcium carbonate is probably limiting the conversion, due to a reduced (bi)carbonate activity. The mechanisms for the aqueous carbonation of wollastonite were shown to be similar to those reported previously for an industrial residue and a Mg-silicate. The carbonation of wollastonite proceeds rapidly relative to Mg-silicates, with a maximum conversion in 15 min of 70% at 200C, 20 bar CO2 partial pressure and a particle size of <38 μm. The obtained insight in the reaction mechanisms enables the energetic and economic assessment of CO2 sequestration by wollastonite carbonation, which forms an essential next step in its further development

  6. Carbon fiber CVD coating by carbon nanostructured for space materials protection against atomic oxygen

    Science.gov (United States)

    Pastore, Roberto; Bueno Morles, Ramon; Micheli, Davide

    2016-07-01

    In recent years, the emphasis in space research has been shifting from space exploration to commercialization of space. In order to utilize space for commercial purposes it is necessary to understand the low earth orbit (LEO) space environment where most of the activities will be carried out. The studies on the LEO environment are mainly focused towards understanding the effect of atomic oxygen (AO) on spacecraft materials. In the first few shuttle flights, materials looked frosty because they were actually being eroded and textured: AO reacts with organic materials on spacecraft exteriors, gradually damaging them. When a spacecraft travel in LEO (where crewed vehicles and the International Space Station fly), the AO formed from the residual atmosphere can react with the spacecraft surfaces, causing damage to the vehicle. Polymers are widely used in space vehicles and systems as structural materials, thermal blankets, thermal control coatings, conformal coatings, adhesives, lubricants, etc. Exposure of polymers and composites to the space environment may result in different detrimental effects via modification of their chemical, electrical, thermal, optical and mechanical properties as well as surface erosion. The major degradation effects in polymers are due to their exposure to atomic oxygen, vacuum ultraviolet and synergistic effects, which result in different damaging effects by modification of the polymer's chemical properties. In hydrocarbon containing polymers the main AO effect is the surface erosion via chemical reactions and the release of volatile reaction products associated with the mass loss. The application of a thin protective coating to the base materials is one of the most commonly used methods of preventing AO degradation. The purpose is to provide a barrier between base material and AO environment or, in some cases, to alter AO reactions to inhibit its diffusion. The effectiveness of a coating depends on its continuity, porosity, degree of

  7. Validation of International Atomic Energy Agency Equipment Performance Requirements

    Energy Technology Data Exchange (ETDEWEB)

    Chiaro, PJ

    2004-02-17

    Performance requirements and testing protocols are needed to ensure that equipment used by the International Atomic Energy Agency (IAEA) is reliable. Oak Ridge National Laboratory (ORNL), through the US Support Program, tested equipment to validate performance requirements protocols used by the IAEA for the subject equipment categories. Performance protocol validation tests were performed in the Environmental Effects Laboratory in the categories for battery, DC power supply, and uninterruptible power supply (UPS). Specific test results for each piece of equipment used in the validation process are included in this report.

  8. Safeguards and legal matters 1996. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all currently valid sales publications of the International Atomic Energy Agency dealing with Safeguards and Legal Matters. Most publications are published in English. Proceedings of conferences, symposia and panels of experts may contain some papers in languages other than English (French, Russian or Spanish), but all of these papers have abstracts in English. It should be noted that prices of books are quoted in Austrian Schillings. The prices do not include local taxes and are subject to change without notice. All books in this catalogue are 16 x 24 cm, paper-bound, unless otherwise stated

  9. Earth sciences 1980-1994. International Atomic Energy Agency Publications

    International Nuclear Information System (INIS)

    This catalogue lists sales publications of the International Atomic Energy Agency dealing with Earth Sciences issued during the period 1969-1994. Most publications are published in English. Proceedings of conferences, symposia and panels of experts may contain some papers in languages other than English (French, Russian or Spanish), but all these papers have abstracts in English. It should be noted that prices of books are quoted in Austrian Schillings. The prices do not include local taxes and are subject to change without notice. All books in this catalogue are 16 x 24 cm, paper-bound, unless otherwise stated

  10. Selective determination of antimony(III) and antimony(V) with ammonium pyrrolidinedithiocarbamate, sodium diethyldithiocarbamate and dithizone by atomic-absorption spectrometry with a carbon-tube atomizer.

    Science.gov (United States)

    Kamada, T; Yamamoto, Y

    1977-05-01

    The extraction behaviour of antimony(III) and antimony(V) with ammonium pyrrolidinedithiocarbamate, sodium diethyldithiocarbamate and dithizone in organic solvents has been investigated by means of frameless atomic-absorption spectrophotometry with a carbon-tube atomizer. The selective extraction of antimony(III) and differential determination of antimony(III) and antimony(V) have been developed. With ammonium pyrrolidinedithiocarbamate and methyl isobutyl ketone, when the aqueous phase/solvent volume ratio is 50 ml/10 ml and the injection volume in the carbon tube is 20 mul, the sensitivity for antimony is 0.2 ng/ml for 1% absorption. The relative standard deviations are ca. 2%. Interferences by many metal ions can be prevented by masking with EDTA. The proposed methods have been applied satisfactorily to determination of antimony(III) and antimony(V) in various types of water. PMID:18962096

  11. The International Atomic Energy Agency: Structure, organs, and practice

    International Nuclear Information System (INIS)

    As a special organization of the UN system the International Atomic Energy Agency (IAEA) bears world-wide responsibility for the promotion of peaceful uses of nuclear power as well as for the control of preventing its misuse for non-peaceful purposes. Based on this fundamental objective of the IAEA a survey of structure, organs and practice of the Agency is given. Particularly, those special programmes are detailed which are of importance to the use of nuclear power for energy generation, and those contributions of the IAEA are concerned which it has to make as the international control authority to prevent the proliferation of nuclear weapons. In conclusions, the future activities of the IAEA and the cooperation of the GDR with the IAEA are dealt with. (author)

  12. Disposal of transuranic solid waste using Atomics International Molten Salt Combustion Process

    International Nuclear Information System (INIS)

    The Atomics International Molten Salt Combustion Process for disposal of transuranic solid waste utilizes a molten salt to combust organic materials, to trap inorganic substances including transuranics, and to react chemically with acidic gases formed during combustion. Subsequent processing of the melt in an aqueous system produces three products: (1) ash, which includes the transuranics, (2) salt, which is recycled to the combustor, and (3) solid sodium chloride for disposal. The transuranics are readily leached from the ash and separated via ion exchange techniques. The leached ash is the second solid process product requiring disposal. No liquid wastes are produced in the process. The reductions in weight and volume are 82 and 98 percent respectively, if one considers the products from the process only. (U.S.)

  13. Atomic carbon in comet atmospheres. Origin and emission spectra

    International Nuclear Information System (INIS)

    A detailed study of neutral carbon emissions is made, to precise the excitation mechanism nature, to determine the production mechanisms and examine wether information on CO and CO2 molecule abundance could be deduced, or wether another source must be looked for. After an exhaustive study of excitation rates necessary for theoretical intensity calculation, a new effect has been discovered, and which acts on the atom excitation rates, via their distribution on the fundamental hyperfine levels. On the other hand, the strong dependency of the excitation rate ratio with heliocentric velocity and with the hypothesis which is made on the atom population initial distribution has been revealed. The carbon abundance in all the comets of the initial sample has been calculated, then compared to the water one revealing two groups of comets. Then an abundance criterium to remove the CO and CO2 molecules from the carbon potential-parents in the Bradfield comet has been used while CO is the best candicate for C(3P) and C(1D) atom production in the West, Kohoutek and Bennet comets (but to certain conditions). The important conclusion is that, while the relative abundance (C2/OH, CN/OH,...) of the minor carbon compounds were constant, the CO relative abundance varies from an object to the other, probably an effect due to repeated passage of some comets near the sun

  14. Atomic and electronic structure of divacancies in carbon nanotubes

    Science.gov (United States)

    Berber, Savas; Oshiyama, Atsushi

    2008-04-01

    We present atomic and electronic structure of divacancies in carbon nanotubes, which is calculated using the density functional theory. Divacancies in carbon nanotubes self-heal by spontaneous reconstructions, which consist of concerted bond formations. Divacancy formation energies EDV , which strongly depend on the divacancy orientation with respect to the tube axis, are in the range of 2.8 4.3 eV for favorable orientations in the nanotubes of 4 9Å diameter, making divacancies more probable than monovacancies in carbon nanotubes. Defect related states lead to a higher density of states around the Fermi level. Semiconducting nanotubes develop midgap levels that may adversely affect the functionality of carbon nanotube based devices. Our spin polarized density functional calculations show that the exchange splitting of defect-related bands in nonsemiconducting defective nanotubes leads to net spin polarizations of ρ↑-ρ↓≤0.5μB per divacancy for some divacancy orientations.

  15. Adsorption of methylene blue and Congo red from aqueous solution by activated carbon and carbon nanotubes.

    Science.gov (United States)

    Szlachta, M; Wójtowicz, P

    2013-01-01

    This study was conducted to determine the adsorption removal of dyes by powdered activated carbon (PAC, Norit) and multi-walled carbon nanotubes (MWCNTs, Chinese Academy of Science) from an aqueous solution. Methylene blue (MB) and Congo red (CR) were selected as model compounds. The adsorbents tested have a high surface area (PAC 835 m(2)/g, MWCNTs 358 m(2)/g) and a well-developed porous structure which enabled the effective treatment of dye-contaminated waters and wastewaters. To evaluate the capacity of PAC and MWCNTs to adsorb dyes, a series of batch adsorption experiments was performed. Both adsorbents exhibited a high adsorptive capacity for MB and CR, and equilibrium data fitted well with the Langmuir model, with the maximum adsorption capacity up to 400 mg/g for MB and 500 mg/g for CR. The separation factor, RL, revealed the favorable nature of the adsorption process under experimental conditions. The kinetics of adsorption was studied at various initial dye concentrations and solution temperatures. The pseudo-second-order model was used for determining the adsorption kinetics of MB and CR. The data obtained show that adsorption of both dyes was rapid in the initial stage and followed by slower processing to reach the plateau. The uptake of dyes increased with contact time, irrespective of their initial concentration and solution temperature. However, changes in the solution temperature did not significantly influence dye removal. PMID:24292474

  16. International Atomic Energy Agency. Highlights of activities. September 1993

    International Nuclear Information System (INIS)

    This document describes the most important activities of the International Atomic Energy Agency during the period September 1992 - September 1993, in particular in the following areas: (i) nuclear power; (ii) nuclear fuel cycle; (iii) radioactive waste management; (iv) comparative assessment of energy sources; (v) IAEA laboratory activities; (vi) nuclear applications in the food industry and in agriculture; (vii) human health applications of nuclear techniques, especially in the treatment and prevention of diseases and in the analysis of health problems related to the environment; (viii) industry and earth sciences; (ix) physical and chemical sciences; (x) radiation protection; (xi) safety of nuclear installations; (xii) safeguards and non-proliferation activities; (xiii) activities in the area of public and technical information such as the International Nuclear Information System (INIS) and other IAEA computerized databases and reference systems, the publication Nuclear Fusion, a monthly scientific journal of articles on thermonuclear fusion research and development, and the organization of meetings on atomic energy; and (xiv) a description of the Agency's technical assistance activities, including financial data

  17. Multi-walled carbon nanotubes in aqueous phytic acid for enhancing biosensor

    International Nuclear Information System (INIS)

    The poor dispersion of carbon based nanomaterials without strong acid pretreatment in aqueous solution is a fundamental problem, limiting its applications in biology-related fields. A good dispersion of multi-walled carbon nanotubes (MWCNTs) in water was realized by 50 wt.% phytic acid (PA) solution. As an application case, the PA–MWCNTs dispersion in aqueous solution was used for the immobilization of horseradish peroxidase (HRP) and its direct electrochemistry was realized. The constructed biosensor has a sound limit of detection, wide linear range, and high affinity for hydrogen peroxide (H2O2) as well as being free from interference of co-existing electro-active species. (papers)

  18. Multi-walled carbon nanotubes in aqueous phytic acid for enhancing biosensor

    Science.gov (United States)

    Guo, Xiaoyu; Miao, Yun; Ye, Pingping; Wen, Ying; Yang, Haifeng

    2014-04-01

    The poor dispersion of carbon based nanomaterials without strong acid pretreatment in aqueous solution is a fundamental problem, limiting its applications in biology-related fields. A good dispersion of multi-walled carbon nanotubes (MWCNTs) in water was realized by 50 wt.% phytic acid (PA) solution. As an application case, the PA-MWCNTs dispersion in aqueous solution was used for the immobilization of horseradish peroxidase (HRP) and its direct electrochemistry was realized. The constructed biosensor has a sound limit of detection, wide linear range, and high affinity for hydrogen peroxide (H2O2) as well as being free from interference of co-existing electro-active species.

  19. Surface heterogeneity effects of activated carbons on the kinetics of paracetamol removal from aqueous solution

    Science.gov (United States)

    Ruiz, B.; Cabrita, I.; Mestre, A. S.; Parra, J. B.; Pires, J.; Carvalho, A. P.; Ania, C. O.

    2010-06-01

    The removal of a compound with therapeutic activity (paracetamol) from aqueous solutions using chemically modified activated carbons has been investigated. The chemical nature of the activated carbon material was modified by wet oxidation, so as to study the effect of the carbon surface chemistry and composition on the removal of paracetamol. The surface heterogeneity of the carbon created upon oxidation was found to be a determinant in the adsorption capability of the modified adsorbents, as well as in the rate of paracetamol removal. The experimental kinetic data were fitted to the pseudo-second order and intraparticle diffusion models. The parameters obtained were linked to the textural and chemical features of the activated carbons. After oxidation the wettability of the carbon is enhanced, which favors the transfer of paracetamol molecules to the carbon pores (smaller boundary layer thickness). At the same time the overall adsorption rate and removal efficiency are reduced in the oxidized carbon due to the competitive effect of water molecules.

  20. The Cold Atom Laboratory: a facility for ultracold atom experiments aboard the International Space Station

    Science.gov (United States)

    Aveline, David; CAL Team

    2016-05-01

    Spread across the globe there are many different experiments in cold quantum gases, enabling the creation and study of novel states of matter, as well as some of the most accurate inertial sensors currently known. The Cold Atom Laboratory (CAL), being built at NASA's Jet Propulsion Laboratory (JPL), will be a multi-user facility that will allow the first study of ultracold quantum gases in the microgravity conditions of the International Space Station (ISS). The microgravity environment offers a wealth of advantages for studies of cold atoms, including expansion into extremely weak traps and achieving unearthly cold temperatures. It will also enable very long interaction times with released samples, thereby enhancing the sensitivity of cold atom interferometry. We will describe the CAL mission objectives and the flight hardware architecture. We will also report our ongoing technology development for the CAL mission, including the first microwave evaporation to Bose-Einstein condensation (BEC) on a miniaturized atom chip system, demonstrated in JPL's CAL Ground Testbed. We will present the design, setup, and operation of two experiments that reliably generate and probe BECs and dual-species mixtures of Rb-87 and K-39 (or K-41). CAL is scheduled to launch to the ISS in 2017. The CAL mission is supported by NASA's SLPS and ISS-PO. This research was carried out at the Jet Propulsion Laboratory, California Institute of Technology, under Contract with the National Aeronautics and Space Administration.

  1. Thermal properties of carbon black aqueous nanofluids for solar absorption

    Directory of Open Access Journals (Sweden)

    Han Dongxiao

    2011-01-01

    Full Text Available Abstract In this article, carbon black nanofluids were prepared by dispersing the pretreated carbon black powder into distilled water. The size and morphology of the nanoparticles were explored. The photothermal properties, optical properties, rheological behaviors, and thermal conductivities of the nanofluids were also investigated. The results showed that the nanofluids of high-volume fraction had better photothermal properties. Both carbon black powder and nanofluids had good absorption in the whole wavelength ranging from 200 to 2,500 nm. The nanofluids exhibited a shear thinning behavior. The shear viscosity increased with the increasing volume fraction and decreased with the increasing temperature at the same shear rate. The thermal conductivity of carbon black nanofluids increased with the increase of volume fraction and temperature. Carbon black nanofluids had good absorption ability of solar energy and can effectively enhance the solar absorption efficiency.

  2. Roles of Mineralogical Phases in Aqueous Carbonation of Steelmaking Slag

    Directory of Open Access Journals (Sweden)

    Huining Zhang

    2016-05-01

    Full Text Available Mineralogical phases of steelmaking slags have significant influences on the carbonation of the slags. In this paper, the effects of temperature and reaction time on the conversion of calcium-related phases and the carbonation degree of a slag sample were studied. The experimental conditions were a liquid-to-solid ratio of 20 mL/g, a carbon dioxide flow rate of 1 L/min and a slag particle size of 38–75 μm. The results show that the optimum carbonation temperature and reaction time are 60 °C and 90 min, respectively, and calcite phase content is about 26.78% while the conversion rates of Ca3Al2O6, CaSiO3, Ca2SiO4 and free CaO are about 40%, 42.46%, 51% and 100%, respectively, and the carbon dioxide sequestration efficiency is about 170 g/kg slag.

  3. Carbon nanotube forests growth using catalysts from atomic layer deposition

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Bingan; Zhang, Can; Esconjauregui, Santiago; Xie, Rongsi; Zhong, Guofang; Robertson, John [Department of Engineering, University of Cambridge, Cambridge CB3 0FA (United Kingdom); Bhardwaj, Sunil [Istituto Officina dei Materiali-CNR Laboratorio TASC, s.s. 14, km 163.4, I-34012 Trieste (Italy); Sincrotone Trieste S.C.p.A., s.s. 14, km 163.4, I-34149 Trieste (Italy); Cepek, Cinzia [Istituto Officina dei Materiali-CNR Laboratorio TASC, s.s. 14, km 163.4, I-34012 Trieste (Italy)

    2014-04-14

    We have grown carbon nanotubes using Fe and Ni catalyst films deposited by atomic layer deposition. Both metals lead to catalytically active nanoparticles for growing vertically aligned nanotube forests or carbon fibres, depending on the growth conditions and whether the substrate is alumina or silica. The resulting nanotubes have narrow diameter and wall number distributions that are as narrow as those grown from sputtered catalysts. The state of the catalyst is studied by in-situ and ex-situ X-ray photoemission spectroscopy. We demonstrate multi-directional nanotube growth on a porous alumina foam coated with Fe prepared by atomic layer deposition. This deposition technique can be useful for nanotube applications in microelectronics, filter technology, and energy storage.

  4. Interpretation of Hund's multiplicity rule for the carbon atom.

    Science.gov (United States)

    Hongo, Kenta; Maezono, Ryo; Kawazoe, Yoshiyuki; Yasuhara, Hiroshi; Towler, M D; Needs, R J

    2004-10-15

    Hund's multiplicity rule is investigated for the carbon atom using quantum Monte Carlo methods. Our calculations give an accurate account of electronic correlation and obey the virial theorem to high accuracy. This allows us to obtain accurate values for each of the energy terms and therefore to give a convincing explanation of the mechanism by which Hund's rule operates in carbon. We find that the energy gain in the triplet with respect to the singlet state is due to the greater electron-nucleus attraction in the higher spin state, in accordance with Hartree-Fock calculations and studies including correlation. The method used here can easily be extended to heavier atoms. PMID:15473780

  5. TRIGA International - History of Training Research Isotope production General Atomics

    International Nuclear Information System (INIS)

    TRIGA conceived at GA in 1956 by a distinguished group of scientists including Edward Teller and Freeman Dyson. First TRIGA reactor Mk-1 was commissioned on 3 may 1958 at G.A. Characteristic feature of TRIGA reactors is inherent safety: Sitting can be confinement or conventional building. TRIGA reactors are the most prevalent in the world: 67 reactors in 24 countries. Steady state powers up to 14 MWt, pulsing up to 22,000 MWt. To enlarge the scope of its manufactured products, CERCA engaged in a Joint Venture with General Atomics, and in July 1995 a new Company was founded: TRIGA INTERNATIONAL SAS (50% GA, 50% CERCA; Head Office: Paris (France); Sales offices: GA San Diego (Ca, USA) and CERCA Lyon (France); Manufacturing plant: CERCA Romans. General Atomics ID: founded in 1955 at San Diego, California, by General Dynamics; status: Privately held corporation; owners: Neal and Linden Blue; business: High technology research, design, manufacturing, and production for industry and Government in the U.S. and overseas; locations: U.S., Germany, Japan, Australia, Thailand, Morocco; employees: 5,000. TRIGA's ID: CERCA is a subsidiary of AREVA, born in November 05, 1957. Activities: fuel manufacture for research reactor, equipment and components for high-energy physics, radioactive sources and reference sources; plants locations: Romans and Pierrelatte (France); total strength: 180. Since the last five years TRIGA has manufactured and delivered more than 800 fuel elements with a door to door service. TRIGA International has the experience to manufacture all types of TRIGA fuel: standard fuel elements, instrumented fuel elements, fuel followed control rods, geometry: 37.3 mm (1.47 in.), 35.8 mm (1.4 in), 13 mm (0.5 in), chemical Composition: U w% 8.5, 12, 20, 30 and 45 w/o, erbium and no erbium. TRIGA International is on INL's approved vendor list (ISO 9000/NQA) and is ready to meet any TRIGA fuel needs either in the US or worldwide

  6. Carbon fiber CVD coating by carbon nanostructured for space materials protection against atomic oxygen

    Science.gov (United States)

    Pastore, Roberto; Bueno Morles, Ramon; Micheli, Davide

    2016-07-01

    In recent years, the emphasis in space research has been shifting from space exploration to commercialization of space. In order to utilize space for commercial purposes it is necessary to understand the low earth orbit (LEO) space environment where most of the activities will be carried out. The studies on the LEO environment are mainly focused towards understanding the effect of atomic oxygen (AO) on spacecraft materials. In the first few shuttle flights, materials looked frosty because they were actually being eroded and textured: AO reacts with organic materials on spacecraft exteriors, gradually damaging them. When a spacecraft travel in LEO (where crewed vehicles and the International Space Station fly), the AO formed from the residual atmosphere can react with the spacecraft surfaces, causing damage to the vehicle. Polymers are widely used in space vehicles and systems as structural materials, thermal blankets, thermal control coatings, conformal coatings, adhesives, lubricants, etc. Exposure of polymers and composites to the space environment may result in different detrimental effects via modification of their chemical, electrical, thermal, optical and mechanical properties as well as surface erosion. The major degradation effects in polymers are due to their exposure to atomic oxygen, vacuum ultraviolet and synergistic effects, which result in different damaging effects by modification of the polymer's chemical properties. In hydrocarbon containing polymers the main AO effect is the surface erosion via chemical reactions and the release of volatile reaction products associated with the mass loss. The application of a thin protective coating to the base materials is one of the most commonly used methods of preventing AO degradation. The purpose is to provide a barrier between base material and AO environment or, in some cases, to alter AO reactions to inhibit its diffusion. The effectiveness of a coating depends on its continuity, porosity, degree of

  7. Metallic and semiconducting carbon nanotubes separation using an aqueous two-phase separation technique: a review

    Science.gov (United States)

    Tang, Malcolm S. Y.; Ng, Eng-Poh; Juan, Joon Ching; Ooi, Chien Wei; Ling, Tau Chuan; Woon, Kai Lin; Loke Show, Pau

    2016-08-01

    It is known that carbon nanotubes show desirable physical and chemical properties with a wide array of potential applications. Nonetheless, their potential has been hampered by the difficulties in acquiring high purity, chiral-specific tubes. Considerable advancement has been made in terms of the purification of carbon nanotubes, for instance chemical oxidation, physical separation, and myriad combinations of physical and chemical methods. The aqueous two-phase separation technique has recently been demonstrated to be able to sort carbon nanotubes based on their chirality. The technique requires low cost polymers and salt, and is able to sort the tubes based on their diameter as well as metallicity. In this review, we aim to provide a review that could stimulate innovative thought on the progress of a carbon nanotubes sorting method using the aqueous two-phase separation method, and present possible future work and an outlook that could enhance the methodology.

  8. Experimental measurement and modeling of the rate of absorption of carbon dioxide by aqueous ammonia

    DEFF Research Database (Denmark)

    Darde, Victor Camille Alfred; van Well, Willy J.M.; Fosbøl, Philip Loldrup;

    2011-01-01

    In this work, the rate of absorption of carbon dioxide by aqueous ammonia solvent has been studied by applying a newly built wetted wall column. The absorption rate in aqueous ammonia was measured at temperatures from 279 to 304K for 1 to 10wt% aqueous ammonia with loadings varying from 0 to 0.8mol......CO2/molNH3. The absorption rate in 30wt% aqueous mono-ethanolamine (MEA) was measured at 294 and 314K with loadings varying from 0 to 0.4 as comparison.It was found that at 304K, the rate of absorption of carbon dioxide by 10wt% NH3 solvent was comparable to the rates for 30wt% MEA at 294 and 314K (a.......The rate of absorption decreases strongly with decreasing ammonia concentrations and increasing CO2 loadings.The rate of absorption of carbon dioxide by aqueous ammonia solvent was modeled using the measurements of the unloaded solutions and the zwitter-ion mechanism. The model could successfully predict...

  9. International Nuclear Information System. 1988-2002. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications and products of the International Atomic Energy Agency dealing with the International Nuclear Information System (INIS), and issued during the period 1 January 1990 - 31 July 2002. Most publications are issued in English, though some are also available in other languages. This is noted as E for English, F for French, G for German, R for Russian and S for Spanish before the relevant ISBN number. Some INIS Reference Series publications are available in electronic form from the INIS Clearinghouse. For more details on the INIS publications programme, please visit the INIS web site mentioned above

  10. Comprehensive analysis of direct aqueous mineral carbonation using dissolution enhancing organic additives.

    OpenAIRE

    Bonfils, Benjamin; Julcour-Lebigue, Carine; Guyot, François; Bodénan, Françoise; Chiquet, Pierre; Bourgeois, Florent

    2012-01-01

    Direct aqueous mineral carbonation using organic anions has been presented by many as a promising strategy for mineral carbonation, on the basis that additives such as oxalate increase the rate and extent of dissolution of magnesium silicates several folds. Through geochemical modelling and detailed solid characterization, this paper discusses and extends our current understanding of this process. The role of disodium oxalate as a dissolution enhancing agent for olivine is thoroughly examined...

  11. Separation of Th from aqueous solutions using activated carbon

    International Nuclear Information System (INIS)

    Since the last century, thorium has been extensively used in a variety of applications. These applications produce various gaseous, liquid and solid wastes containing isotopes of thorium. Liquid wastes are freed into the surface or the underground waters of mines. Solid and liquid wastes are also produced during nuclear fuel production. Direct toxicity of thorium is low due to its stability at ambient temperatures; however thorium fine powder is self-ignitable to thorium oxide. When thorium nitrate enters living organisms it is mainly localized in liver, spleen and marrow and it precipitates in a hydroxide form. Investigations concerning the removal or minimization of the thorium concentration in the waste waters are of considerable importance environmental point of view. Adsorption is an important technique in separation and purification processes. Among many types of adsorbent materials, activated carbons are the most widely used, because of their large adsorptive capacity and low cost. Activated carbons are unique adsorbents because of their extended surface area, microporous structure, high adsorption capacity and high degree of surface reactivity. Separation and purification processes based on adsorption technique are also important in nuclear industry where activated carbon is often used for the separation of metal ions from solutions, due to its selective adsorption, high radiation stability and high purity. The activated carbons used in this study were prepared by the chemical activation of acrylic fiber. The chemical composition of acrylic fiber is a copolymer of acrylonitrile-vinyl acetate is called also poliacrylonitryl fiber. The effects of carbonization conditions resulting activated carbon were examined. Precursor/activating agent (KOH and ZnCl2) ratio and carbonization temperature were investigated for the preparation of adsorbent. Adsorption experiments were carried out by a batch technique. The adsorption of thorium was studied as a function of

  12. Internal motions in three-body bosonic Thomson atoms

    International Nuclear Information System (INIS)

    A three-body bosonic Thomson atom, namely a system of three charged bosons in a harmonic trap, with a very large Wigner parameter, has been studied. The states with zero angular momentum and even parity denoted as 0n+ have been calculated and analysed; the basic modes of excitation of this system have been revealed. It was found that each lower 0n+ state (n is from 1 to 5) has its own means of internal motion. Although the size of the system is very sensitive to the strength of the trap, the other features are found to be insensitive to the strength if the system remains in the Wigner regime. The breathing mode was found to be the easiest to excite. (author)

  13. International Atomic Energy Agency Publications. Catalogue 1980-1995

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency issued from 1980 up to the end of 1995 an still available. Some earlier titles which form part of an established series or are still considered of importance have been included. Most Agency publications are issued in English, though some are also available in Chinese, French, Russian or Spanish. This is noted as C for Chinese, E for English, F for French, R for Russian and S For Spanish by the relevant ISBN number. Proceedings of conferences, symposia, seminars and panels, of experts contain papers in their original language (English, French, Russian or Spanish) with abstracts in English and in the original language

  14. Safeguards and legal matters 1994. International Atomic Energy Agency Publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with Safeguards and Legal Matters issued during the period 1970-1994. Most publications are published in English, through some are also available in French, Russian and Spanish. Proceedings of conferences, symposia and panels of experts may contain some papers in languages other than English (French, Russian or Spanish), but all of these papers have abstracts in English. If publications are also available in other languages than English, this is noted as C for Chinese, F for French, R for Russian and S for Spanish by the relevant ISBN number. It should be noted that prices of books are quoted in Austrian Schillings. The prices do not include local taxes and are subject to change without notice. All books in this catalogue are 16 x 24 cm, paper-bound, unless otherwise stated

  15. Proposal for the International Atomic Energy Agency Training Course

    International Nuclear Information System (INIS)

    The Hanford Site has hosted similar activities, including both Hanford Summits I and II. The Hanford Summits were two-day televised events to discuss the commitment of the current Presidential administration to the environmental restoration of the Hanford Site. Public involvement and strategic issues established from Hanford Summit I include: Regulatory issues, training and education, economic development and partnership, and technology transfer. Hanford Summit II provided a summary of how Secretary of Energy O'Leary is proceeding on the above strategic issues. The DOE and Westinghouse School for Environmental Excellence frequently offers a six-week course for environmental professionals and workers. Approximately thirty to forty individuals attend the training course, which provides training in environmental regulation compliance. The Hanford Site has hosted two previous International Atomic Energy Agency training courses. The courses lasted two weeks and had approximately eight to ten participants. Nuclear Material Management and Neutron Monitoring were the courses hosted by the Hanford Site

  16. Performance of multiwall carbon nanotubes for removal phenol from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Mohamad Hadi Dehghani

    2013-05-01

    Conclusion: It is concluded that carbon nanotubes being effective in a wide range of pH, short time to reach equilibrium and the absence of competing ions on the absorption process can be used effectively in removing phenol from aqueous solution.

  17. Formation and atomic structure of tetrahedral carbon onion produced by electron-beam irradiation

    International Nuclear Information System (INIS)

    Full text: Various fullerene structures has been designed and produced after the discovery of C60. These fullerene materials are good candidates as nanoscale devises such as single-electron devices, nano-diode, nano-transistor, nano-ball bearing and insulator lubricant. The onion structures, which generally consist of some quasi-spherical fullerene group, are also discovered and studied in detail. The tetrahedral carbon onions had been calculated to be unstable compared to the spherical onions due to the rigidity. The purpose of the present work is to produce new carbon onion by high-energy electron-irradiation on amorphous carbon at 1250 kV, and to investigate atomic structures and stability of the new carbon onion cluster by high-resolution electron microscopy (HREM) and molecular orbital/mechanics calculations. To confirm the structure model from HREM data, HREM image simulation were carried out. The tetrahedral carbon onion was successfully produced by high-energy electron-irradiation. A HREM image of tetrahedral carbon onion would consist of pentagonal and hexagonal rings. The HREM result indicates that new fullerene structures formed into the carbon onion. Molecular mechanics calculations (MM2), semi-empirical molecular orbital calculations (PM3), and density functional theory (DFT) were used to get structure optimization about first and second internal shell. The energy levels and density of states were also calculated by the first principles method (DV-Xα). The smallest tetrahedral onion in the HREM image agreed well with the proposed structure model of C84atC276. Each vertex consists of a hexagonal ring, and three pentagonal rings exist around the vertex along the edge. In summary, the tetrahedral carbon cluster was produced by energy transfer of electron-irradiation, and the new atomic structure model of tetrahedral carbon onion was proposed. The electronic structures were also calculated theoretically. Copyright (2002) Australian Society for Electron

  18. Process monitoring in support of International Atomic Energy Agency safeguards

    International Nuclear Information System (INIS)

    A review of previous efforts in process monitoring for safeguards was conducted. Previous efforts touched on various concepts and a few specific applications, but none was comprehensive in addressing all aspects of a process monitoring application for safeguards. This report develops prototypical process monitoring concepts that can be incorporated into the International Atomic Energy Agency's (IAEA's) general safeguards approach for fuel reprocessing plants. This effort considers existing approaches, recognizing limitations and needed improvements. Prototypical process monitoring applications are developed and proposed for implementation and demonstration in the Integrated Equipment Test facility, which is located at the Oak Ridge National Laboratory. The specific information needed to accomplish the process monitoring objectives are defined, and the mechanics for obtaining that information are described. Effort is given to the identification and assessment of potential impacts and benefits associated with process monitoring concepts, with particular attention to IAEA, state, and plant operator interests. The historical development of process monitoring is described and the implications of using process monitoring in international safeguards are discussed. Specific process process monitoring applications for demonstration in the IET facility are developed in Sects. 6 through 14. 1 fig

  19. Carbon dust formation under heavy atomic hydrogen irradiation

    International Nuclear Information System (INIS)

    Dust formation mechanism in plasma-material surface interactions has been investigated by using high pressure inductively coupled plasmas (ICPs), which have a feature of high atomic particle flux (atomic hydrogen flux: ∼1024 m-2s-1, ion flux: ∼1021 m-2s-1). Experiments have been conducted in argon/hydrogen mixture plasma irradiation to graphite targets. In the present experiments, physical sputtering is not expected and the dominant erosion process of graphite target is chemical sputtering by atomic hydrogen irradiation. Carbon dust particles with various shapes have been observed on the graphite target irradiated by argon/hydrogen plasma. It is found that the shapes of the dust particles are strongly related to the target surface temperature, graphite spherical particle when the surface temperature is below ∼1100 K and polyhedral particle like diamond when above ∼1100 K. It is also shown that the carbon dust formation and growth does not choose the surface materials. The number density of dust formed decreases as the plasma input power decreases or the distance between the target and induction coil increases, while the weight loss remains almost the same even though the input power and distance between the target and induction coil are varied. The size of dust particles increases as increasing surface temperature. These experimental results indicate that the dust growth is strongly related to surface temperature. (author)

  20. Nanoporous carbon synthesized from sol-gel template for adsorbing gibberellic acid in aqueous solution

    International Nuclear Information System (INIS)

    A novel method, based on dynamic carbonization and silica template formed by sol-gel, was developed to prepare nanoporous carbon materials with tailored pore structures. The effects of the sol-gel reaction and carbonization process on the final nanoporous carbon product were investigated by pore features such as specific surface area, the total pore volume, and pore size distribution, which were systemically characterized by iodine index, transmission electron microscopy, and nitrogen adsorption. The experimental results indicate that the pore structures of the prepared nanoporous carbon are tunable on the nano-scale by controlling the preparation process in the proposed method. The nanoporous carbon prepared under the optimal conditions has a high total pore volume of 1.26 cm3/g, a large specific surface area of 1744 m2/g, and a maximal adsorption capacity of 9.2 mg/g to gibberellic acid in aqueous solution, which is nearly 6 times that of commercial activated carbon. Highlights: → Silica formed by sol-gel as template for nanoporous carbon preparation. → Pore structures are tunable on the nano-scale. → High total pore volume and large specific surface developing. → Adsorption of gibberellic acid in aqueous solution carrying out.

  1. Voronoi analysis of the short–range atomic structure in iron and iron–carbon melts

    International Nuclear Information System (INIS)

    In this work, we simulated the atomic structure of liquid iron and iron–carbon alloys by means of ab initio molecular dynamics. Voronoi analysis was used to highlight changes in the close environments of Fe atoms as carbon concentration in the melt increases. We have found, that even high concentrations of carbon do not affect short–range atomic order of iron atoms — it remains effectively the same as in pure iron melts

  2. Probing the elastic response of microalga Scenedesmus dimorphus in dry and aqueous environments through atomic force microscopy

    International Nuclear Information System (INIS)

    With the re-emergence of microalgae as a replacement feedstock for petroleum-derived oils, researchers are working to understand its chemical and mechanical behavior. In this work, the mechanical properties of microalgae, Scenedesmus dimorphus, were investigated at the subcellular level to determine the elastic response of cells that were in an aqueous and dried state using nano-scale indentation through atomic force microscopy. The elastic modulus of single-celled S. dimorphus cells increased over tenfold from an aqueous state to a dried state, which allows us to better understand the biophysical response of microalgae to stress.

  3. Probing the elastic response of microalga Scenedesmus dimorphus in dry and aqueous environments through atomic force microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Warren, K. M.; Mpagazehe, J. N.; Higgs, C. F., E-mail: prl@andrew.cmu.edu, E-mail: higgs@andrew.cmu.edu [Department of Mechanical Engineering, Carnegie Mellon University, 5000 Forbes Ave, Pittsburgh, Pennsylvania 15213 (United States); LeDuc, P. R., E-mail: prl@andrew.cmu.edu, E-mail: higgs@andrew.cmu.edu [Department of Mechanical Engineering, Carnegie Mellon University, 5000 Forbes Ave, Pittsburgh, Pennsylvania 15213 (United States); Departments of Biomedical Engineering and Biological Sciences, Carnegie Mellon University, 5000 Forbes Ave., Pittsburgh, Pennsylvania 15213 (United States)

    2014-10-20

    With the re-emergence of microalgae as a replacement feedstock for petroleum-derived oils, researchers are working to understand its chemical and mechanical behavior. In this work, the mechanical properties of microalgae, Scenedesmus dimorphus, were investigated at the subcellular level to determine the elastic response of cells that were in an aqueous and dried state using nano-scale indentation through atomic force microscopy. The elastic modulus of single-celled S. dimorphus cells increased over tenfold from an aqueous state to a dried state, which allows us to better understand the biophysical response of microalgae to stress.

  4. The International Atomic Energy Agency Nuclear Security Education Strategies

    International Nuclear Information System (INIS)

    The threat of nuclear terrorism has not diminished. In response to the concerns of States, an international nuclear security framework has emerged through the establishment of a number of legally binding and non-binding international instruments which obligates or commits States to carry out a number of actions to protect against nuclear terrorism. In this context, the need for human resource development programmes in nuclear security was underscored at several International Atomic Energy Agency (IAEA) General Conferences and Board of Governors' Meetings. In the pursuit of this need, the IAEA provides a comprehensive nuclear security training programme to States on a regular basis, and has developed a concept that seeks to effectively pass ownership of nuclear security knowledge and skills to States through the establishment of a Nuclear Security Support Centre. In addition, the IAEA has developed a technical guidance titled IAEA Nuclear Security Series No. 12 - Educational Programme in Nuclear Security that consists of a model of a Master of Science (M.Sc.) and assists educational institutions to provide nuclear security education. The article sets out IAEA efforts in the area of nuclear security training and education, including the assistance to States for establishing a Nuclear Security Support Centre. It underlines the objective and content of the IAEA Nuclear Security Series No. 12, discusses different concepts on how to establish nuclear security at universities and, emphasizes on the IAEA efforts to assist educational and research institutions, and other stake holders to enhance global nuclear security by developing, sharing and promoting excellence in nuclear security education. (author)

  5. Formation of isomers of anionic hemiesters of sugars and carbonic acid in aqueous medium.

    Science.gov (United States)

    Dos Santos, Vagner B; Vidal, Denis T R; Francisco, Kelliton J M; Ducati, Lucas C; do Lago, Claudimir L

    2016-06-16

    Hemiesters of carbonic acid can be freely formed in aqueous media containing HCO3(-)/CO2 and mono- or poly-hydroxy compounds. Herein, (13)C NMR spectroscopy was used to identify isomers formed in aqueous solutions of glycerol (a prototype compound) and seven carbohydrates, as well as to estimate the equilibrium constant of formation (Keq). Although both isomers are formed, glycerol 1-carbonate corresponds to 90% of the product. While fructose and ribose form an indistinct mixture of isomers, the anomers of d-glucopyranose 6-carbonate correspond to 74% of the eight isomers of glucose carbonate that were detected. The values of Keq for the disaccharides sucrose (4.3) and maltose (4.2) are about twice the values for the monosaccharides glucose (2.0) and fructose (2.3). Ribose (Keq = 0.89)-the only sugar without a significant concentration of a species containing a -CH2OH group in an aqueous solution-resulted in the smallest Keq. On the basis of the Keq value and the concentrations of HCO3(-) and glucose in blood, one can anticipate a concentration of 2-4 µmol L(-1) for glucose 6-carbonate, which corresponds to ca. of 10% of its phosphate counterpart (glucose 6-phosphate). PMID:27111726

  6. Determination of adhesion between single Aspergillus niger spores in aqueous solutions using an atomic force microscope.

    Science.gov (United States)

    Wargenau, Andreas; Kwade, Arno

    2010-07-01

    The interaction force between single cells in contact is of high interest in various interdisciplinary fields of biotechnology, for instance, in cultivation or biofilm formation. A method for the determination of adhesion forces between two single Aspergillus niger spores in different aqueous solutions was established in this study. Adhesion force distributions were determined at three different sodium chloride concentrations and two different pH values using an atomic force microscope (AFM). It was pointed out that adhesion data can be described by log-normal density functions, of which corresponding parameters have been estimated. Using the knowledge of distribution shape, the influence of the environmental condition on the mean values of adhesion force could be studied quantitatively. The highest value of 0.95 nN was observed at pH 2.5 and an ionic strength of 0.5 mol L(-1). Decreasing the ionic strength to 0.05 mol L(-1) decreases the adhesion force mean for about 25%. Increasing the pH value to pH 5 at a sodium chloride concentration of 0.154 mol L(-1) entails a decrease of adhesion from 0.88 to 0.56 nN. These results qualitatively agree with the absolute value of the expected surface potential of Aspergillus niger spores, which is much higher at pH 5 and should take more effect at lower concentrations of counterions. PMID:20387816

  7. Simultaneous leaching and carbon sequestration in constrained aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Phelps, Tommy Joe [ORNL; Moon, Ji Won [ORNL; Roh, Yul [Chonnam National University, Gwangju; Cho, Kyu Seong [ORNL

    2011-01-01

    The behavior of metal ions leaching and precipitated mineral phases of metal-rich fly ash (FA) was examined in order to evaluate microbial impacts on carbon sequestration and metal immobilization. The leaching solutions consisted of aerobic deionized water (DW) and artificial eutrophic water (AEW) that was anaerobic, organic- and mineral-rich, and higher salinity as is typical of bottom water in eutrophic algae ponds. The Fe- and Ca-rich FAs were predominantly composed of quartz, mullite, portlandite, calcite, hannebachite, maghemite, and hematite. After 86 days, only Fe and Ca contents exhibited a decrease in leaching solutions while other major and trace elements showed increasing or steady trends in preference to the type of FA and leaching solution. Ca-rich FA showed strong carbon sequestration efficiency ranging up to 32.3 g CO(2)/kg FA after 86 days, corresponding to almost 65% of biotic carbon sequestration potential under some conditions. Variations in the properties of FAs such as chemical compositions, mineral constituents as well as the type of leaching solution impacted CO(2) capture. Even though the relative amount of calcite increased sixfold in the AEW and the relative amount of mineral phase reached 37.3 wt% using Ca-rich FA for 86 days, chemical sequestration did not accomplish simultaneous precipitation and sequestration of several heavy metals.

  8. Corrosion behavior of aluminum doped diamond-like carbon thin films in NaCl aqueous solution.

    Science.gov (United States)

    Khun, N W; Liu, E

    2010-07-01

    Aluminum doped diamond-like carbon (DLC:Al) thin films were deposited on n-Si(100) substrates by co-sputtering a graphite target under a fixed DC power (650 W) and an aluminum target under varying DC power (10-90 W) at room temperature. The structure, adhesion strength and surface morphology of the DLC:Al films were characterized by X-ray photoelectron spectroscopy (XPS), micro-scratch testing and atomic force microscopy (AFM), respectively. The corrosion performance of the DLC:Al films was investigated by means of potentiodynamic polarization testing in a 0.6 M NaCl aqueous solution. The results showed that the polarization resistance of the DLC:Al films increased from about 18 to 30.7 k(omega) though the corrosion potentials of the films shifted to more negative values with increased Al content in the films. PMID:21128496

  9. Kinetics of carbon dioxide removal by aqueous diamines

    Energy Technology Data Exchange (ETDEWEB)

    Bindwal, A.B.; Vaidya, P.D.; Kenig, E.Y. [Inst. of Chemical Technology, Bombay (India). Dept. of Chemical Engineering

    2011-05-01

    Because of the presence of one or more primary or secondary amino groups, solvents containing diamines have a good potential for CO{sub 2} capture. In the present work, the CO{sub 2} reactions with two diamines, namely N-(2-aminoethyl)ethanolamine (AEEA) and piperazine (PZ), in aqueous solutions are investigated using a stirred-cell reactor. The reaction pathways are described using the zwitterion and the termolecular mechanism. Solution densities and viscosities are measured. The investigated reactions belong to the fast reaction regime systems. It is found that the CO{sub 2} reaction with AEEA is of the second order with respect to AEEA within the temperature range 298-308 K and amine concentration range 1.5-3 kmol/m{sup 3}. At 303 K. the reaction rate constant equals 8530 m{sup 6}/(kmol{sup 2} s). The value of the second-order rate constant for the CO{sub 2} reaction with PZ is found to be 25.800 m{sup 3}/(kmol s) at 303 K.

  10. Mineral sequestration of carbon dioxide in San Carlos olivine: An atomic level reaction study

    Science.gov (United States)

    Nunez, Ryan

    Since the late 19th century, atmospheric carbon dioxide (CO2) levels have been steadily on the rise. Approximately one third of all human emissions come from fossil fuel power plants. As countries become more dependent on electrical energy and bring on line new power plants, these atmospheric CO2 levels will continue to rise, generating strong environmental concern. Potential avenues to address this problem convert the CO2 from the gaseous phase to a liquid, supercritical fluid, or solid state and store it. Oceans, subsurface reservoirs such as depleted oil fields, and terrestrial carbon pools have all been suggested. The essential problem with all of these possible solutions is the issue of permanency. Mineral sequestration of CO2 is a candidate technology for reducing the amount of anthropogenic CO2 that is being released into the atmosphere. Olivine (e.g. forsterite, Mg2SiO4) is a widely available mineral that reacts with CO2 to form magnesite (MgCO3) and silica (SiO2). Magnesite is capable of immobilizing CO2 over geological time periods. Thus the issue of permanency has been addressed. The most promising mineral sequestration process developed to date is aqueous solution mineral carbonation. The solid/aqueous solution reaction interface provides insight to the mechanisms that govern the carbonation reactivity of olivine. Study of these mechanisms at the atomic level is critically important to facilitate engineering new processes that will enhance the reactivity of olivine with CO2 bearing media and to lower process costs. The study of the olivine carbonation reaction herein can be divided into three separate areas of research. The first area is a comprehensive study of olivine under conditions of electron irradiation. Analyzing radiation damage is critical to the verification and reliability of data collected from the samples using electron beam techniques. The next area of research is the analysis of the reaction layer composition and structure using High

  11. Electroanalytical performance of carbon films with near-atomic flatness.

    Science.gov (United States)

    Ranganathan, S; McCreery, R L

    2001-03-01

    Physicochemical and electrochemical characterization of carbon films obtained by pyrolyzing a commercially available photoresist has been performed. Photoresist spin-coated on to a silicon wafer was pyrolyzed at 1,000 degrees C in a reducing atmosphere (95% nitrogen and 5% hydrogen) to produce conducting carbon films. The pyrolyzed photoresist films (PPF) show unusual surface properties compared to other carbon electrodes. The surfaces are nearly atomically smooth with a root-mean-square roughness of pyrolysis to evaluate the electroanalytical utility of PPF. Heterogeneous electron-transfer kinetics of various redox systems were evaluated. For Ru(NH3)6(3+/2+), Fe(CN)6(3-/4-), and chlorpromazine, fresh PPF surfaces show electron-transfer rates similar to those on GC, but for redox systems such as Fe3+/2+, ascorbic acid, dopamine, and oxygen, the kinetics on PPF are slower. Very weak interactions between the PPF surface and these redox systems lead to their slow electron-transfer kinetics. Electrochemical anodization results in a simultaneous increase in background current, adsorption, and electron-transfer kinetics. The PPF surfaces can be chemically modified via diazonium ion reduction to yield a covalently attached monolayer. Such a modification could help in the preparation of low-cost, high-volume analyte-specific electrodes for diverse electroanalytical applications. Overall, pyrolysis of the photoresist yields an electrode surface with properties similar to a very smooth version of glassy carbon, with some important differences in surface chemistry. PMID:11289433

  12. A Theoretical Simulation of Deformed Carbon Nanotubes with Adsorbed Metal Atoms: Enhanced Reactivity by Deformation

    OpenAIRE

    Hosoya, Naoki; Kusakabe, Koichi; Maheswari, S. Uma

    2010-01-01

    First-principles simulations were performed to investigate reaction of carbon nanotubes with adsorbed metal atoms. Mechanical modification of their structures enhances chemical reactivity of carbon nanotubes. Adsorption of a tungsten, tantalum, or niobium atom on a (5, 0) nanotube with a Stone-Wales defect was shown to have characteristically strong chemisorption. Bond-breaking in the carbon-carbon network and formation of a local metal-carbon complex were observed during the simulation. Adso...

  13. Determination of Mercury in Aqueous and Geologic Materials by Continuous Flow-Cold Vapor-Atomic Fluorescence Spectrometry (CVAFS)

    Science.gov (United States)

    Hageman, Philip L.

    2007-01-01

    New methods for the determination of total mercury in geologic materials and dissolved mercury in aqueous samples have been developed that will replace the methods currently (2006) in use. The new methods eliminate the use of sodium dichromate (Na2Cr2O7 ?2H2O) as an oxidizer and preservative and significantly lower the detection limit for geologic and aqueous samples. The new methods also update instrumentation from the traditional use of cold vapor-atomic absorption spectrometry to cold vapor-atomic fluorescence spectrometry. At the same time, the new digestion procedures for geologic materials use the same size test tubes, and the same aluminum heating block and hot plate as required by the current methods. New procedures for collecting and processing of aqueous samples use the same procedures that are currently (2006) in use except that the samples are now preserved with concentrated hydrochloric acid/bromine monochloride instead of sodium dichromate/nitric acid. Both the 'old' and new methods have the same analyst productivity rates. These similarities should permit easy migration to the new methods. Analysis of geologic and aqueous reference standards using the new methods show that these procedures provide mercury recoveries that are as good as or better than the previously used methods.

  14. Carbon Fiber Reinforced Carbon Composite Valve for an Internal Combustion Engine

    Science.gov (United States)

    Rivers, H. Kevin (Inventor); Ransone, Philip O. (Inventor); Northam, G. Burton (Inventor)

    1999-01-01

    A carbon fiber reinforced carbon composite valve for internal combustion engines and the like formed of continuous carbon fibers throughout the valve's stem and head is disclosed. The valve includes braided carbon fiber material over axially aligned unidirectional carbon fibers forming a valve stem; the braided and unidirectional carbon fibers being broomed out at one end of the valve stem forming the shape of the valve head; the valve-shaped structure being densified and rigidized with a matrix of carbon containing discontinuous carbon fibers: and the finished valve being treated to resist oxidation. Also disclosed is a carbon matrix plug containing continuous and discontinuous carbon fibers and forming a net-shape valve head acting as a mandrel over which the unidirectional and braided carbon fibers are formed according to textile processes. Also disclosed are various preform valves and processes for making finished and preform carbon fiber reinforced carbon composite valves.

  15. A carbon powder-nanotube composite cathode for non-aqueous lithium-air batteries

    International Nuclear Information System (INIS)

    Highlights: • A composite cathode made of carbon powder and nanotubes is proposed. • The new electrode enables a substantial increase in the capacity and cycle number. • The improved performance can be mainly attributed to the enlarged pore spaces. - Abstract: Carbon powder has been predominately used to form cathode electrodes for non-aqueous lithium-air batteries, mainly due to their large specific surface area. An issue, however, with carbon-powder based cathodes is the large oxygen transport resistance due to limited pore spaces resulting from the packing with nanosized spherical particles, leading to a practical discharge capacity much lower than the theoretical value. The present work addresses this issue by proposing a composite cathode made of carbon powder and nanotubes for non-aqueous lithium-air batteries. The discharge performance characterizations show that the discharge capacity of the cathode with mixed carbon materials increases with an increase in the ratio of carbon nanotubes to powder. At the ratio of 1:1, the highest volumetric and the gravimetric capacity are achieved, which are respectively 67.2% and 36.3% higher than those with the cathode made of pure carbon powder. It is further demonstrated that the battery with the composite cathode at a fixed capacity of 1.0 mA h/cm2 exhibits a cycle life of up to 50 cycles, which is nearly twice the cycle number of the battery with its cathode made of pure carbon powder. The mechanism leading to the improved performance can be mainly attributed to the improved oxygen transport as the result of enlarged pore spaces with an appropriate composition of spherical carbon powder and cylindrical carbon nanotubes

  16. Removal of Uranium From Aqueous Solution by Carbon Nanotubes.

    Science.gov (United States)

    Yu, Jing; Wang, Jianlong

    2016-10-01

    The adsorption of uranium onto carbon nanotubes (CNTs) was investigated. The effect of solution pH, contact time, initial uranium concentration, and temperature on the adsorption capacity of uranium was determined. CNTs were characterized by using scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder x-ray diffraction (XRD), Raman spectra, and the Fourier infrared spectra (FTIR). The diameters of the CNTs varied from 10 to 50 nm in diameter and 1 ~ 2 μm in length. FTIR spectra analysis indicated that carboxyl groups were involved in adsorption of U(VI) by CNTs. The experimental results showed that U(VI) adsorption onto CNTs reached equilibrium within 10 min, and the removal efficiency was 95% at pH = 5. The adsorption kinetics of U(VI) could be described by a pseudo first-order kinetic model. The adsorption isotherm conformed to the Slips model. The adsorption process was spontaneous and endothermic. PMID:27575349

  17. Removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution using rice husk-based activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Taha, Mohd F., E-mail: faisalt@petronas.com.my; Shaharun, Maizatul S. [Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia); Shuib, Anis Suhaila, E-mail: anisuha@petronas.com.my; Borhan, Azry [Chemical Engineering Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia)

    2014-10-24

    An attempt was made to investigate the potential of rice husk-based activated carbon as an alternative low-cost adsorbent for the removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Rice husk-based activated carbon was prepared via treatment of rice husk with NaOH followed by the carbonization process at 400°C for 2 hours. Three samples, i.e. raw rice husk, rice husk treated with NaOH and rice husk-based activated carbon, were analyzed for their morphological characteristics using field-emission scanning electron microscope/energy dispersive X-ray (FESEM/EDX). These samples were also analyzed for their carbon, hydrogen, nitrogen, oxygen and silica contents using CHN elemental analyzer and FESEM/EDX. The porous properties of rice husk-based activated carbon were determined by Brunauer-Emmett-Teller (BET) surface area analyzer, and its surface area and pore volume were 255 m{sup 2}/g and 0.17 cm{sup 2}/g, respectively. The adsorption studies for the removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution were carried out at a fixed initial concentration of metal ion (150 ppm) with variation amount of adsorbent (rice husk-based activated carbon) as a function of varied contact time at room temperature. The concentration of each metal ion was analyzed using atomic absorption spectrophotometer (AAS). The results obtained from adsorption studies indicate the potential of rice husk as an economically promising precursor for the preparation of activated carbon for removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Isotherm and kinetic model analyses suggested that the experimental data of adsorption studies fitted well with Langmuir, Freundlich and second-order kinetic models.

  18. Removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution using rice husk-based activated carbon

    International Nuclear Information System (INIS)

    An attempt was made to investigate the potential of rice husk-based activated carbon as an alternative low-cost adsorbent for the removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Rice husk-based activated carbon was prepared via treatment of rice husk with NaOH followed by the carbonization process at 400°C for 2 hours. Three samples, i.e. raw rice husk, rice husk treated with NaOH and rice husk-based activated carbon, were analyzed for their morphological characteristics using field-emission scanning electron microscope/energy dispersive X-ray (FESEM/EDX). These samples were also analyzed for their carbon, hydrogen, nitrogen, oxygen and silica contents using CHN elemental analyzer and FESEM/EDX. The porous properties of rice husk-based activated carbon were determined by Brunauer-Emmett-Teller (BET) surface area analyzer, and its surface area and pore volume were 255 m2/g and 0.17 cm2/g, respectively. The adsorption studies for the removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution were carried out at a fixed initial concentration of metal ion (150 ppm) with variation amount of adsorbent (rice husk-based activated carbon) as a function of varied contact time at room temperature. The concentration of each metal ion was analyzed using atomic absorption spectrophotometer (AAS). The results obtained from adsorption studies indicate the potential of rice husk as an economically promising precursor for the preparation of activated carbon for removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Isotherm and kinetic model analyses suggested that the experimental data of adsorption studies fitted well with Langmuir, Freundlich and second-order kinetic models

  19. Removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution using rice husk-based activated carbon

    Science.gov (United States)

    Taha, Mohd F.; Shuib, Anis Suhaila; Shaharun, Maizatul S.; Borhan, Azry

    2014-10-01

    An attempt was made to investigate the potential of rice husk-based activated carbon as an alternative low-cost adsorbent for the removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Rice husk-based activated carbon was prepared via treatment of rice husk with NaOH followed by the carbonization process at 400°C for 2 hours. Three samples, i.e. raw rice husk, rice husk treated with NaOH and rice husk-based activated carbon, were analyzed for their morphological characteristics using field-emission scanning electron microscope/energy dispersive X-ray (FESEM/EDX). These samples were also analyzed for their carbon, hydrogen, nitrogen, oxygen and silica contents using CHN elemental analyzer and FESEM/EDX. The porous properties of rice husk-based activated carbon were determined by Brunauer-Emmett-Teller (BET) surface area analyzer, and its surface area and pore volume were 255 m2/g and 0.17 cm2/g, respectively. The adsorption studies for the removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution were carried out at a fixed initial concentration of metal ion (150 ppm) with variation amount of adsorbent (rice husk-based activated carbon) as a function of varied contact time at room temperature. The concentration of each metal ion was analyzed using atomic absorption spectrophotometer (AAS). The results obtained from adsorption studies indicate the potential of rice husk as an economically promising precursor for the preparation of activated carbon for removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Isotherm and kinetic model analyses suggested that the experimental data of adsorption studies fitted well with Langmuir, Freundlich and second-order kinetic models.

  20. International Nuclear Information System 1983-1996. International Atomic Energy Agency Publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with the International Nuclear Information System (INIS). INIS was established in 1969 to announced the scientific literature published worldwide on the peaceful uses of nuclear energy. All books are published in English. It should be noted that prices of books are quoted in Austrian Schillings. The prices do not include local taxes and are subject to change without notice. All books in this catalogue are 21 x 30 cm, paper-bound, unless otherwise stated. In addition all books in this catalogue, except for the INIS Input Training Kit, are available on microfiche. For information on the microfiche versions, contact the INIS Clearinghouse of the IAEA

  1. 4. All-Russian (international) scientific conference. Physicochemical processes during selection of atoms and molecules. Collection of reports

    International Nuclear Information System (INIS)

    The reports of the 4. All-Russian (international) scientific conference: Physicochemical processes during selection of atoms and molecules, are presented. The conference took place in Zvenigorod, 4-8 October, 1999. Contents of the reports are the following: laser isotope separation of molecules and atoms; isotopic selection of molecules and atoms in the field of centrifugal forces; selection of molecules by means of rectification and isotopic exchange methods; separation of isotopes by ion cyclotron-resonance method, in electric discharge and electromagnetic field; change in physical properties of substances which variation of their natural isotopic composition; use of isotopes in pharmacy preparation; status of experimental and diagnostic technique; certain promising methods of selection of atoms and molecules. The problems of laser separation of uranium isotopes, separation of carbon isotopes by multi-photon selective dissociation are discussed. The procedures permitting production of isotopes with high concentration and efficiency are developed

  2. RICE BRAN CARBON: AN ALTERNATIVE TO COMMERCIAL ACTIVATED CARBON FOR THE REMOVAL OF HEXAVALENT CHROMIUM FROM AQUEOUS SOLUTION

    OpenAIRE

    Syed Hadi Hasan; Deeksha Ranjan

    2010-01-01

    Rice bran carbon (RBC) prepared from rice bran (an agricultural waste) was successfully utilized for the removal of hexavalent chromium from aqueous solution. The potentiality of RBC was tested and compared with commercial activated carbon (CAC), and it was found that RBC removed 95% of hexavalent chromium at pH 2, 1000 µM Cr(VI) concentration, temperature 30 oC, and adsorbent dose of 2 g/L. The maximum uptake of total chromium obtained by applying the Langmuir isotherm model was 138.88 mg/g ...

  3. Development of large scale internal reforming molten carbonate fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Sasaki, A.; Shinoki, T.; Matsumura, M. [Mitsubishi Electric Corp., Hyogo (Japan)

    1996-12-31

    Internal Reforming (IR) is a prominent scheme for Molten Carbonate Fuel Cell (MCFC) power generating systems in order to get high efficiency i.e. 55-60% as based on the Higher Heating Value (HHV) and compact configuration. The Advanced Internal Reforming (AIR) technology has been developed based on two types of the IR-MCFC technology i.e. Direct Internal Reforming (DIR) and Indirect Internal Reforming (DIR).

  4. Carbon nanofibers with radially grown graphene sheets derived from electrospinning for aqueous supercapacitors with high working voltage and energy density

    Science.gov (United States)

    Zhao, Lei; Qiu, Yejun; Yu, Jie; Deng, Xianyu; Dai, Chenglong; Bai, Xuedong

    2013-05-01

    Improvement of energy density is an urgent task for developing advanced supercapacitors. In this paper, aqueous supercapacitors with high voltage of 1.8 V and energy density of 29.1 W h kg-1 were fabricated based on carbon nanofibers (CNFs) and Na2SO4 electrolyte. The CNFs with radially grown graphene sheets (GSs) and small average diameter down to 11 nm were prepared by electrospinning and carbonization in NH3. The radially grown GSs contain between 1 and a few atomic layers with their edges exposed on the surface. The CNFs are doped with nitrogen and oxygen with different concentrations depending on the carbonizing temperature. The supercapacitors exhibit excellent cycling performance with the capacity retention over 93.7% after 5000 charging-discharging cycles. The unique structure, possessing radially grown GSs, small diameter, and heteroatom doping of the CNFs, and application of neutral electrolyte account for the high voltage and energy density of the present supercapacitors. The present supercapacitors are of high promise for practical application due to the high energy density and the advantages of neutral electrolyte including low cost, safety, low corrosivity, and convenient assembly in air.

  5. Synthesis and application of highly active dithiooxamide fictionalised multi-walled carbon nanotubes toward mercury removal from aqueous solution

    International Nuclear Information System (INIS)

    Highly sensitive and accurate method has been applied for removal of toxic mercury(II) ions in aqueous solution, using synthesized nanosorbent. Determination of mercury(II) was carried out by flame atomic absorption spectrometer. A nanosorbent MWCNT was synthesized by the reaction of dithiooxamide with functionalized multi-walled carbon nanotubes. Initially, the surface of the multi-walled carbon nanotubes was oxidized by a mixture of nitric and sulfuric acids and then was functionalized using thionyl chloride. The ligand has been attached to the multi-walled carbon nanotubes in a somewhat shorter time and lower temperature than previous reported methods. The sorbent was characterized by Fourier transmission infrared and scanning electron microscopy. In this research, the effect of different parameters in removal of mercury(II) ions by nanosorbent, such as, pH, amount of nanosorbent, time and concentration of Hg(II), was investigated. Experiments show that the new MWCNT with loading amount of 1.02 mmol g-1 is a powerful sorbent for removing the Hg(II) ions from water. (author)

  6. Decolorisation of Reactive Red 120 Dye by Using Single-Walled Carbon Nanotubes in Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Edris Bazrafshan

    2013-01-01

    Full Text Available Dyes are one of the most hazardous chemical compound classes found in industrial effluents and need to be treated since their presence in water bodies reduces light penetration, precluding the photosynthesis of aqueous flora. In the present study, single-walled carbon nanotubes (SWCNTs was used as an adsorbent for the successful removal of Reactive Red 120 (RR-120 textile dye from aqueous solutions. The effect of various operating parameters such as initial concentration of dye, contact time, adsorbent dosage and initial pH was investigated in order to find the optimum adsorption conditions. Equilibrium isotherms were used to identify the possible mechanism of the adsorption process. The optimum pH for removing of RR-120 dye from aqueous solutions was found to be 5 and for this condition maximum predicted adsorption capacity for RR-120 dye was obtained as 426.49 mg/g. Also, the equilibrium data were also fitted to the Langmuir, Freundlich and BET equilibrium isotherm models. It was found that the data fitted to BET (R2=0.9897 better than Langmuir (R2=0.9190 and Freundlich (R2=0.8819 model. Finally it was concluded that the single-walled carbon nanotubes can be used for dye removal from aqueous solutions.

  7. The effect of surface oxides on multi-walled carbon nanotube aqueous colloidal properties

    Science.gov (United States)

    Smith, Billy

    Carbonaceous nanomaterials are being produced and integrated into consumer products and specialized applications at an accelerating rate. Recently, however, concerns have increased about the environmental, health and safety risks of these nanomaterials, particularly those chemically functionalized to enhance their aqueous colloidal stability and biocompatibility. In this dissertation research, I have investigated the role that surface-oxide concentration plays in the aqueous colloidal stability of multi-walled carbon nanotubes (MWCNTs), a prominent class of engineered nanomaterials. To vary the concentration of surface oxides on the MWCNTs' surface, pristine (unmodified) tubes were treated with a wet-chemical oxidant (e.g., HNO3, H2SO4 /HNO3, KMnO4); the concentration of surface oxides imparted was measured by x-ray photoelectron spectroscopy (XPS). In conjunction with XPS, previously developed chemical derivatization techniques were used to determine the distribution of hydroxyl, carboxyl, and carbonyl functional groups present on the MWCNTs' surface. The length distribution and structural integrity of pristine and oxidized MWCNTs were characterized using atomic force microscopy and transmission electron microscopy, respectively. To examine the aqueous colloidal stability and aggregation properties of oxidized MWCNTs, sedimentation and time-resolved dynamic light scattering (TR-DLS) experiments were conducted on neat (i.e., ideal) suspensions prepared by prolonged sonication of MWCNTs in Milli-Q water. Over a range of environmentally relevant pH values (4--9) and electrolyte (NaCL, CaCl2) concentrations (0.001--1.000 M), the aggregation and colloidal properties of MWCNTs were found to agree with the basic tenants of DLVO theory, in that ( i) more highly oxidized, negatively charged MWCNTs remained stable over a wider range of solution conditions than lowly oxidized tubes, ( ii) oxidized MWCNTs adhered to the empirical Schulze-Hardy rule, and (iii) in early

  8. Current-induced dynamics in carbon atomic contacts

    Directory of Open Access Journals (Sweden)

    Jing-Tao Lü

    2011-12-01

    Full Text Available Background: The effect of electric current on the motion of atoms still poses many questions, and several mechanisms are at play. Recently there has been focus on the importance of the current-induced nonconservative forces (NC and Berry-phase derived forces (BP with respect to the stability of molecular-scale contacts. Systems based on molecules bridging electrically gated graphene electrodes may offer an interesting test-bed for these effects.Results: We employ a semi-classical Langevin approach in combination with DFT calculations to study the current-induced vibrational dynamics of an atomic carbon chain connecting electrically gated graphene electrodes. This illustrates how the device stability can be predicted solely from the modes obtained from the Langevin equation, including the current-induced forces. We point out that the gate offers control of the current, independent of the bias voltage, which can be used to explore current-induced vibrational instabilities due the NC/BP forces. Furthermore, using tight-binding and the Brenner potential we illustrate how Langevin-type molecular-dynamics calculations including the Joule heating effect for the carbon-chain systems can be performed. Molecular dynamics including current-induced forces enables an energy redistribution mechanism among the modes, mediated by anharmonic interactions, which is found to be vital in the description of the electrical heating.Conclusion: We have developed a semiclassical Langevin equation approach that can be used to explore current-induced dynamics and instabilities. We find instabilities at experimentally relevant bias and gate voltages for the carbon-chain system.

  9. The Unique Hoyle State of the Carbon Atom

    Directory of Open Access Journals (Sweden)

    Thorvaldsen, Steinar

    2015-05-01

    Full Text Available The famous astronomer Fred Hoyle (1915-2001 started his research career as an atheist. Hoyle’s most important contribution to astrophysics is the theory of nucleosynthesis, i.e. the idea that chemical elements such as carbon can form in stars on the basis of hydrogen and helium. Essentially here was his prediction that the carbon core has a state with a specific energy which is precisely adapted to the basic fusion process. This result was one of the most important breakthroughs in modern astrophysics, and the so called Hoyle state has become a cornerstone for state-ofthe- art nuclear theory. The calculations he made, eventually revealed a fine-tuning of the universe. Hoyle’s work in this area supported the anthropic principle that the universe was fine-tuned so that intelligent life would be possible. It is said that what really made him conclude that creation demanded intelligence, were his calculations of the special properties of the carbon atom. This shook his atheism fundamentally [1, p. 57]. In this paper we describe this discovery.

  10. Adsorption of tetracycline from aqueous solutions onto multi-walled carbon nanotubes with different oxygen contents

    OpenAIRE

    Fei Yu; Jie Ma; Sheng Han

    2014-01-01

    Oxidized multi-walled carbon nanotubes (MWCNTs) with different oxygen contents were investigated for the adsorption of tetracycline (TC) from aqueous solutions. As the surface oxygen content of the MWCNTs increased, the maximum adsorption capacity and adsorption coefficient of TC increased to the largest values and then decreased. The relation can be attributed to the interplay between the nanotubes' dispersibility and the water cluster formation upon TC adsorption. The overall adsorption kin...

  11. Effective Degradation of Aqueous Tetracycline Using a Nano-TiO2/Carbon Electrocatalytic Membrane

    OpenAIRE

    Zhimeng Liu; Mengfu Zhu; Zheng Wang; Hong Wang; Cheng Deng; Kui Li

    2016-01-01

    In this work, an electrocatalytic membrane was prepared to degrade aqueous tetracycline (TC) using a carbon membrane coated with nano-TiO2 via a sol-gel process. SEM, XRD, EDS, and XPS were used to characterize the composition and structure of the electrocatalytic membrane. The effect of operating conditions on the removal rate of tetracycline was investigated systematically. The results show that the chemical oxygen demand (COD) removal rate increased with increasing residence time while it ...

  12. Slow reactivation of lyophilized bovine carbonic anhydrase upon dissolution in aqueous solution studied by radiotracer techniques

    International Nuclear Information System (INIS)

    Carbonic anhydrase undergoes reversible denaturation upon lyophilization. Full reactivation requires 30-60 min equilibration time following dissolution in aqueous buffers. The recombination of the Zn2+ cofactor with the active site, investigated by 65Zn tracer studies, is clearly shown to account for only the initial stage of the reactivation process and amounts to only a few per cent of the total reactivation. (author)

  13. An important atomic process in the CVD growth of graphene: Sinking and up-floating of carbon atom on copper surface

    International Nuclear Information System (INIS)

    By density functional theory (DFT) calculations, the early stages of the growth of graphene on copper (1 1 1) surface are investigated. At the very first time of graphene growth, the carbon atom sinks into subsurface. As more carbon atoms are adsorbed nearby the site, the sunken carbon atom will spontaneously form a dimer with one of the newly adsorbed carbon atoms, and the formed dimer will up-float on the top of the surface. We emphasize the role of the co-operative relaxation of the co-adsorbed carbon atoms in facilitating the sinking and up-floating of carbon atoms. In detail: when two carbon atoms are co-adsorbed, their co-operative relaxation will result in different carbon–copper interactions for the co-adsorbed carbon atoms. This difference facilitates the sinking of a single carbon atom into the subsurface. As a third carbon atom is co-adsorbed nearby, it draws the sunken carbon atom on top of the surface, forming a dimer. Co-operative relaxations of the surface involving all adsorbed carbon atoms and their copper neighbors facilitate these sinking and up-floating processes. This investigation is helpful for the deeper understanding of graphene synthesis and the choosing of optimal carbon sources or process.

  14. International bulletin on atomic and molecular data for fusion. No. 58

    International Nuclear Information System (INIS)

    The International Bulletin on Atomic and Molecular Data for Fusion is prepared by the Atomic and Molecular Data Unit of the International Atomic Energy Agency. It is distributed free of charge by the IAEA to assist in the development of fusion research and technology. In part 1, the Atomic and Molecular Data Information System (AMDIS) is presented. In Part 2, the indexed papers are listed separately for structure and spectra, atomic and molecular collisions and surface interactions. Part 3 contains all the bibliographic data for both the indexed and non-indexed references. Finally, the Author Index (part 4) refers to the bibliographic references contained in part 3

  15. International bulletin on atomic and molecular data for fusion. No. 59

    International Nuclear Information System (INIS)

    The International Bulletin on Atomic and Molecular Data for Fusion is prepared by the Atomic and Molecular Data Unit of the International Atomic Energy Agency. It is distributed free of charge by the IAEA to assist in the development of fusion research and technology. In part 1, the Atomic and Molecular Data Information System (AMDIS) is presented. In Part 2, the indexed papers are listed separately for structure and spectra, atomic and molecular collisions and surface interactions. Part 3 contains all the bibliographic data for both the indexed and non-indexed references. Finally, the Author Index (part 4) refers to the bibliographic references contained in part 3

  16. Energy consumption and net CO2 sequestration of aqueous mineral carbonation

    International Nuclear Information System (INIS)

    Aqueous mineral carbonation is a potentially attractive sequestration technology to reduce CO2 emissions. The energy consumption of this technology, however, reduces the net amount of CO2 sequestered. Therefore, the energetic CO2 sequestration efficiency of aqueous mineral carbonation was studied in dependence of various process variables using either wollastonite (CaSiO3) or steel slag as feedstock. For wollastonite, the maximum energetic CO2 sequestration efficiency within the ranges of process conditions studied was 75% at 200C, 20 bar CO2, and a particle size of <38μm. The main energy-consuming process steps were the grinding of the feedstock and the compression of the CO2 feed. At these process conditions, a significantly lower efficiency was determined for steel slag (69%), mainly because of the lower Ca content of the feedstock. The CO2 sequestration efficiency might be improved substantially for both types of feedstock by, e.g., reducing the amount of process water applied and further grinding of the feedstock. The calculated energetic efficiencies warrant a further assessment of the (energetic) feasibility of CO2 sequestration by aqueous mineral carbonation on the basis of a pilot-scale process

  17. Fullerene-containing phases obtained from aqueous dispersions of carbon nanoparticles

    Science.gov (United States)

    Rozhkov, S. P.; Kovalevskii, V. V.; Rozhkova, N. N.

    2007-06-01

    The hydration of fullerenes and shungite carbon nanoclusters in aqueous dispersions at various carbon concentrations is studied on frozen samples by EPR with spin probes. It is found that, for stable dispersions of both substances (at carbon concentrations of 0.1 mg/ml), the probe rotation frequency versus 1/T dependences exhibit a plateau in the range 243 257 K, which is probably associated with the peculiarities of freezing of water localized near hydrophobic structures of carbon nanoclusters. Solid phases isolated from supersaturated aqueous dispersions of fullerenes and shungites by slow evaporation of water at temperatures higher than 0°C are examines by electron diffraction and electron microscopy. It is established that obtained films of fullerenes contain at least two phases: fullerite with a face-centered cubic lattice and a phase similar in interplanar spacing and radically different in distribution of intensities of diffraction peaks. It is concluded that this phase is formed by the interaction of fullerenes and water (an analogous phase is found in shungite carbon films). It is found that the morphology of the new crystal phase is characterized by globules of size 20 to 70 nm, for fullerenes, and 10 to 400 nm for shungites. It is established that processes of crystallization of fullerites and fullerene-containing phases are very sensitive to temperature: a decrease in the temperature (within the range from 40 to 1°C) is accompanied by an increase in the new phase content.

  18. Comparison of capacitive behavior of activated carbons with different pore structures in aqueous and nonaqueous systems

    Institute of Scientific and Technical Information of China (English)

    ZHOU Shao-yun; LI Xin-hai; WANG Zhi-xing; GUO Hua-jun; PENG Wen-jie

    2008-01-01

    The pore structures of two activated carbons from sawdust with KOH activation and coconut-shell with steam activation for supercapacitor were analyzed by N2 adsorption method. The electrochemical properties of both activated carbons in 6mol/L KOH solution and 1mol/L Et4NPF4/PC were compared, and the effect of pore structure on the capacitance was investigated by cyclic voltammetry, AC impedance and charge-discharge measurements. The results indicate that the capacitance mainly depends on effective surface area, but the power property mainly depends on mesoporosity. At low specific current (1A/g), the maximum specific capacitances of 276.3F/g in aqueous system and 123.9F/g in nonaqueous system can be obtained from sawdust activated carbon with a larger surface area of 1808m2/g, but at a high specific current, the specific capacitance of coconut-shell activated carbon with a higher mesoporosity of 75.1% is more excellent. Activated carbon by KOH activation is fitter for aqueous system and that by steam activation is fitter for nonaqueous system.

  19. Effect of Ginkgo biloba Leaves Aqueous Extract on Carbon

    Directory of Open Access Journals (Sweden)

    Hala A.H. Khattab

    2012-07-01

    Full Text Available Bachground: Oxidative stress plays a pivotal role in the pathogenesis and progression of various liver diseases. Ginkgo biloba leaves extract (GbE have been proved to be an effective antioxidant, thereby can contribute to the prevention and treatment of diseases associated with oxidative stress. The present study aimed to investigate the hepatoprotective effect of GbE on acute liver injury induced using carbon tetrachloride (CCl4 in rats. Material and Methods: Hepatotoxicity was induced in male rats by intraperitoneal (i.p injection of CCl4 1mL/ kg body weight (b.w. for every 72 h for 14 days, GbE was administered orally at a dose of 150 mg/kg b.w., daily started two weeks prior to CCl4 injection and continued until the end of the experiment. Results: CCl4 caused acute liver damage in rats, as evidenced by significant increase serum enzymes activities of aspartate and alanine aminotransferase (ALT & AST and alkaline phosphatase (ALP, and hepatic malondialdehyde (MDA, as well as significant decrease in weight gain percent, serum total protein (TP, high-density lipoprotein cholesterol (HDL-C, and hepatic reduced glutathione (GSH. Pretreatment with GbE prior to CCl4 injection elicited hepatoprotetcive activity by significant decreased the activities of liver enzymes and hepatic MDA, and significant increased the levels of TP, and hepatic GSH, as well as induced significant ameliorated in weight gain percent and lipid profile parameters as compared with CCl4 group. Histopathological examination of the liver tissues of CCl4 group represented the presence of hepatic necrosis associated with cells infiltration and vacuolar degeneration of hepatocytes, while the pretreatment with GbE overcome these changes, the majority of the cells tend to be normal.Conclusion: The present findings indicated that the hepatoprotective effect of GbE against CCl4-induced oxidative damage may be due to its potent antioxidant activity. Therefore, GbE could be of potential

  20. Carbon-atom wires produced by nanosecond pulsed laser deposition in a background gas

    OpenAIRE

    Casari, C. S.; Giannuzzi, C. S.; V. Russo

    2016-01-01

    Wires of sp-hybridized carbon atoms are attracting interest for both fundamental aspects of carbon science and for their appealing functional properties. The synthesis by physical vapor deposition has been reported to provide sp-rich carbon films but still needs to be further developed and understood in detail. Here the synthesis of carbon-atom wires (CAWs) has been achieved by nanosecond pulsed laser deposition (PLD) expoliting the strong out-of-equilibrium conditions occurring when the abla...

  1. Contributions for the 6th London international conference on carbon and graphite CARBON 82

    International Nuclear Information System (INIS)

    This report is the compilation of a number of papers prepared by KFA Juelich GmbH for the Sixth London International Conference on Carbon and Graphite CARBON '82 which will be held at London in the Imperial College, 20-24 September, 1982. The presentations deal with objectives of manufacture, nuclear application and reactivity of carboneous materials. (orig./GSCH)

  2. Speciation and detection of arsenic in aqueous samples: A review of recent progress in non-atomic spectrometric methods

    International Nuclear Information System (INIS)

    Highlights: • Compilation of principal official documents and major review articles, including the toxicology and chemistry of As. • Review of non-atomic spectrometric methods for speciation and detection of arsenic in aqueous samples (2005–2013) of the performance of field-usable methods. - Abstract: Inorganic arsenic (As) displays extreme toxicity and is a class A human carcinogen. It is of interest to both analytical chemists and environmental scientists. Facile and sensitive determination of As and knowledge of the speciation of forms of As in aqueous samples are vitally important. Nearly every nation has relevant official regulations on permissible limits of drinking water As content. The size of the literature on As is therefore formidable. The heart of this review consists of two tables: one is a compilation of principal official documents and major review articles, including the toxicology and chemistry of As. This includes comprehensive official compendia on As speciation, sample treatment, recommended procedures for the determination of As in specific sample matrices with specific analytical instrument(s), procedures for multi-element (including As) speciation and analysis, and prior comprehensive reviews on arsenic analysis. The second table focuses on the recent literature (2005–2013, the coverage for 2013 is incomplete) on As measurement in aqueous matrices. Recent As speciation and analysis methods based on spectrometric and electrochemical methods, inductively coupled plasma-mass spectrometry, neutron activation analysis and biosensors are summarized. We have deliberately excluded atomic optical spectrometric techniques (atomic absorption, atomic fluorescence, inductively coupled plasma-optical emission spectrometry) not because they are not important (in fact the majority of arsenic determinations are possibly carried out by one of these techniques) but because these methods are sufficiently mature and little meaningful innovation has been

  3. Atomic Layer Deposition of Zirconium Oxide on Carbon Nanoparticles

    International Nuclear Information System (INIS)

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

  4. Controlling wear failure of graphite-like carbon film in aqueous environment: Two feasible approaches

    Energy Technology Data Exchange (ETDEWEB)

    Wang Yongxin [State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Science, Lanzhou 730000 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100039 (China); Wang Liping, E-mail: lpwang@licp.cas.cn [State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Science, Lanzhou 730000 (China); Xue Qunji [State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Science, Lanzhou 730000 (China)

    2011-02-15

    Friction and wear behaviors of graphite-like carbon (GLC) films in aqueous environment were investigated by a reciprocating sliding tribo-meter with ball-on-disc contact. Film structures and wear scars were studied by scanning electron microscope (SEM), energy dispersive spectroscopy (EDS) and a non-contact 3D surface profiler. A comprehensive wear model of the GLC film in aqueous environment was established, and two feasible approaches to control critical factor to the corresponding wear failure were discussed. Results showed that wear loss of GLC films in aqueous environment was characterized by micro-plough and local delamination. Due to the significant material loss, local delamination of films was critical to wear failure of GLC film in aqueous environment if the film was not prepared properly. The initiation and propagation of micro-cracks within whole films closely related to the occurrence of the films delamination from the interface between interlayer and substrate. The increase of film density by adjusting the deposition condition would significantly reduce the film delamination from substrate, meanwhile, fabricating a proper interlayer between substrate and GLC films to prevent the penetration of water molecules into the interface between interlayer and substrate could effectively eliminate the delamination.

  5. The mechanical property and resistance ability to atomic oxygen corrosion of boron modified carbon/carbon composites

    International Nuclear Information System (INIS)

    Before being densified by chemical vapor deposition, carbon preform was modified by boron. The mechanical property and resistance to atomic oxygen corrosion of carbon/carbon composites were investigated. The results show that fiber surface modification induces the deposition of high texture pyrocarbon and a moderate interfacial transition layer between carbon fibers and matrix carbon. After being modified by boron, the flexural and compressive strength of carbon/carbon composite is significantly increased. The bending curve has been adjusted with obvious pseudo-ductility phenomenon. The resistance ability to atomic oxygen corrosion is improved significantly. The mass loss and corrosion degree of the modified composite are lower than that of pure carbon/carbon composite

  6. Removal of copper and cadmium from aqueous solution using switchgrass biochar produced via hydrothermal carbonization process.

    Science.gov (United States)

    Regmi, Pusker; Garcia Moscoso, Jose Luis; Kumar, Sandeep; Cao, Xiaoyan; Mao, Jingdong; Schafran, Gary

    2012-10-30

    Biochar produced from switchgrass via hydrothermal carbonization (HTC) was used as a sorbent for the removal of copper and cadmium from aqueous solution. The cold activation process using KOH at room temperature was developed to enhance the porous structure and sorption properties of the HTC biochar. The sorption efficiency of HTC biochar and alkali activated HTC biochar (HTCB) for removing copper and cadmium from aqueous solution were compared with commercially available powdered activated carbon (PAC). The present batch adsorption study describes the effects of solution pH, biochar dose, and contact time on copper and cadmium removal efficiency from single metal ion aqueous solutions. The activated HTCB exhibited a higher adsorption potential for copper and cadmium than HTC biochar and PAC. Experiments conducted with an initial metal concentration of 40 mg/L at pH 5.0 and contact time of 24 h resulted in close to 100% copper and cadmium removal by activated HTCB at 2 g/L, far greater than what was observed for HTC biochar (16% and 5.6%) and PAC (4% and 7.7%). The adsorption capacities of activated HTCB for cadmium removal were 34 mg/g (0.313 mmol/g) and copper removal was 31 mg/g (0.503 mmol/g). PMID:22687632

  7. Behavior of pure and modified carbon/carbon composites in atomic oxygen environment

    Institute of Scientific and Technical Information of China (English)

    Xiao-chong Liu; Lai-fei Cheng; Li-tong Zhang; Xin-gang Luan; Hui Mei

    2014-01-01

    Atomic oxygen (AO) is considered the most erosive particle to spacecraft materials in low earth orbit (LEO). Carbon fiber, car-bon/carbon (C/C), and some modified C/C composites were exposed to a simulated AO environment to investigate their behaviors in LEO. Scanning electron microscopy (SEM), AO erosion rate calculation, and mechanical property testing were used to characterize the material properties. Results show that the carbon fiber and C/C specimens undergo significant degradation under the AO bombing. According to the effects of AO on C/C-SiC and CVD-SiC-coated C/C, a condensed CVD-SiC coat is a feasible approach to protect C/C composites from AO degradation.

  8. Boron removal from aqueous solutions by activated carbon impregnated with salicylic acid

    International Nuclear Information System (INIS)

    In this study, the removal of boric acid from aqueous solution by activated carbon impregnated with salicylic acid was studied in batch system. pH, adsorbent amount, initial boron concentration, temperature, shaking rate and salicylic acid film thickness were chosen as parameters. Boron removal efficiencies increased with increasing adsorbent amount, temperature and pH, decreasing initial boron concentration. As thickness of salicylic acid film on activated carbon becomes thin up to 0.088 nm, the efficiency increased, and then, the efficiency decreased with becoming thinner than 0.088 nm of salicylic acid film. Shaking rate was no effect on removal efficiency. In result, it was determined that the use of salicylic acid as an impregnant for activated carbon led to the increase of the amount of boron adsorbed. A lactone ring, being the most appropriate conformation, forms between boric acid and -COOH and -OH groups of salicylic acid

  9. Removal of Lead (II Ions from Aqueous Solutions onto Activated Carbon Derived from Waste Biomass

    Directory of Open Access Journals (Sweden)

    Murat Erdem

    2013-01-01

    Full Text Available The removal of lead (II ions from aqueous solutions was carried out using an activated carbon prepared from a waste biomass. The effects of various parameters such as pH, contact time, initial concentration of lead (II ions, and temperature on the adsorption process were investigated. Energy Dispersive X-Ray Spectroscopy (EDS analysis after adsorption reveals the accumulation of lead (II ions onto activated carbon. The Langmuir and Freundlich isotherm models were applied to analyze equilibrium data. The maximum monolayer adsorption capacity of activated carbon was found to be 476.2 mg g−1. The kinetic data were evaluated and the pseudo-second-order equation provided the best correlation. Thermodynamic parameters suggest that the adsorption process is endothermic and spontaneous.

  10. Atomic Physics 15: Proceedings of the Fifteenth International Conference on Atomic Physics.

    Science.gov (United States)

    van Linden van den Heuvell, H. B.; Walraven, J. T. M.; Reynolds, M. W.

    1997-07-01

    The Table of Contents for the full book PDF is as follows: * Preface * Generation of a "Schrödinger cat" of radiation and observation of its decoherence * Synthesis of entangled states and quantum computing * Entangled states of atomic ions for quantum metrology and computation * Entanglement and indistinguishability: Coherence experiments with photon pairs and triplets * Atom optics as a testing ground for quantum chaos * Coherent ultra-bright XUV lasers and harmonics * Hollow atoms * Interdisciplinary experiments with polarized noble gases * The creation and study of Bose-Einstein condensation in a cold alkali vapor * oscopic quantum phenomena in trapped Bose-condensed gases * Doppler-free spectroscopy of trapped atomic hydrogen * QED and the ground state of helium * Towards coherent atomic samples using laser cooling * Bose-Einstein condensation of a weakly-interacting gas * Zeeman and his contemporaries: Dutch physics around 1900 * Zeeman's great discovery * The Zeeman effect: A tool for atom manipulation * The Zeeman effect a century later: New insights into classical physics * QED effects in few-electron high-Z systems * Lamb shift experiments on high-Z one- and two-electron systems * Fundamental constants of nature * Response of atoms in photonic lattices * Hydrogen-like systems and quantum electrodynamics * New experiments with atomic lattices bound by light * Bloch oscillations of atoms in an optical potential * Quantum decoherence and inertial sensing with atom interferometers * Quantum effects in He clusters * Atoms in super-intense radiation fields * Wave packet dynamics of excited atomic electrons in intense laser fields * Nonlinear laser-electron scattering * Comparing the antiproton and proton and progress toward cold antihydrogen * Author Index

  11. Sorption of a mixture of phenols in aqueous solution with activated carbon

    International Nuclear Information System (INIS)

    The main objective of this work is the sorption of an aqueous mixture of phenol-4 chloro phenol of different concentrations in a molar relationship 1:1 in activated carbon of mineral origin of different nets (10, 20 and 30) and to diminish with it its presence in water. The experimental results show that the removal capacity depends so much of the surface properties of the sorbent like of the physical and chemical properties of the sorbate. In all the cases it was observed that in the aqueous systems of low concentration the 4-chloro phenol are removed in an approximate proportion of 1.2-4 times greater to than phenol, however to concentrations but high both they are removed approximately in the same proportion. (Author)

  12. Comparison of activated carbon and bottom ash removal of reactive dye from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Dincer, A.R.; Gunes, Y.; Karakaya, N.; Gunes, E. [Trakya University, Tekirdag (Turkey). Dept. of Environmental Engineering

    2007-03-15

    The adsorption of reactive dye from synthetic aqueous solution onto granular activated carbon (GAC) and coal-based bottom ash (CBBA) were studied under the same experimental conditions. As an alternative to GAC CBBA was used as adsorbent for dye removal from aqueous solution. The amount of Vertigo Navy Marine (VNM) adsorbed onto CBBA was lower compared with GAC at equilibrium and dye adsorption capacity increased from 0.71 to 3.82 mg g{sup -1}, and 0.73 to 6.35 mg g{sup -1} with the initial concentration of dye from 25 to 300 mg l{sup -1} respectively. The initial dye uptake of CBBA was not so rapid as in the case of GAC and the dye uptake was slow and gradually attained equilibrium.

  13. Experimental verification of segregation of carbon and precipitation of carbides due to deep cryogenic treatment for tool steel by internal friction method

    Energy Technology Data Exchange (ETDEWEB)

    Li, Shaohong, E-mail: uniquelsh@163.com [School of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Min, Na; Li, Junwan; Wu, Xiaochun; Li, Chenhui; Tang, Leilei [School of Materials Science and Engineering, Shanghai University, Shanghai 200072 (China)

    2013-07-15

    This work presents an internal frictional behavior of cold work tool steel subjected to different heat treatment schedules to get insight related to segregation of carbon and refinement of carbide particles due to deep cryogenic treatment. The temperature dependence of internal friction was used to describe the variation of carbon concentration in solid solution of the martensite matrix in successive tempering steps. The results indicate that the carbon atoms segregated to nearby defects forming atomic clusters producing strong interactions, including interstitial carbon atoms themselves and between the interstitial carbon atoms with time-dependent strain field of dislocations because of lattice shrinking and thermodynamic instability of martensite during the deep cryogenic treatment. The clusters act as and grow into nuclei for the formation of fine carbide particle on subsequent tempering that was verified by analyses of TEM micrographs.

  14. Experimental verification of segregation of carbon and precipitation of carbides due to deep cryogenic treatment for tool steel by internal friction method

    International Nuclear Information System (INIS)

    This work presents an internal frictional behavior of cold work tool steel subjected to different heat treatment schedules to get insight related to segregation of carbon and refinement of carbide particles due to deep cryogenic treatment. The temperature dependence of internal friction was used to describe the variation of carbon concentration in solid solution of the martensite matrix in successive tempering steps. The results indicate that the carbon atoms segregated to nearby defects forming atomic clusters producing strong interactions, including interstitial carbon atoms themselves and between the interstitial carbon atoms with time-dependent strain field of dislocations because of lattice shrinking and thermodynamic instability of martensite during the deep cryogenic treatment. The clusters act as and grow into nuclei for the formation of fine carbide particle on subsequent tempering that was verified by analyses of TEM micrographs

  15. Removal of Methylene Blue from Aqueous Solution by Activated Carbon Prepared from Pea Shells (Pisum sativum

    Directory of Open Access Journals (Sweden)

    Ünal Geçgel

    2013-01-01

    Full Text Available An activated carbon was prepared from pea shells and used for the removal of methylene blue (MB from aqueous solutions. The influence of various factors such as adsorbent concentration, initial dye concentration, temperature, contact time, pH, and surfactant was studied. The experimental data were analyzed by the Langmuir and Freundlich models of adsorption. The adsorption isotherm was found to follow the Langmuir model. The monolayer sorption capacity of activated carbon prepared from pea shell for MB was found to be 246.91 mg g−1 at 25 ∘C. Two simplified kinetic models including pseudo-first-order and pseudo-second-order equation were selected to follow the adsorption processes. Kinetic studies showed that the adsorption followed pseudo-second-order kinetic model. Various thermodynamic parameters such as , , and were evaluated. The results in this study indicated that activated carbon prepared from pea shell could be employed as an adsorbent for the removal of MB from aqueous solutions.

  16. Enhanced Oil Recovery from Oil-wet Carbonate Rock by Spontaneous Imbibition of Aqueous Surfactant Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Standnes, Dag Chun

    2001-09-01

    The main theme of this thesis is an experimental investigation of spontaneous imbibition (SI) of aqueous cationic surfactant solution into oil-wet carbonate (chalk- and dolomite cores). The static imbibition process is believed to represent the matrix flow of oil and water in a fractured reservoir. It was known that aqueous solution of C{sub 12}-N(CH{sub 3}){sub 3}Br (C12TAB) was able to imbibe spontaneously into nearly oil-wet chalk material, but the underlying mechanism was not understood. The present work was therefore initiated, with the following objectives: (1) Put forward a hypothesis for the chemical mechanism underlying the SI of C12TAB solutions into oil-wet chalk material based on experimental data and (2) Perform screening tests of low-cost commercially available surfactants for their ability to displace oil by SI of water into oil-wet carbonate rock material. It is essential for optimal use of the surfactant in field application to have detailed knowledge about the mechanism underlying the SI process. The thesis also discusses some preliminary experimental results and suggests mechanisms for enhanced oil recovery from oil-wet carbonate rock induced by supply of thermal energy.

  17. Sorption of a phenols mixture in aqueous solution with activated carbon

    International Nuclear Information System (INIS)

    The constant population growth and the quick industrialization have caused severe damages to our natural aquifer resources for a great variety of organic and inorganic pollutants. Among these they are those phenol compounds that are highly toxic, resistant (to the degradation chemistry) and poorly biodegradable. The phenolic compounds is used in a great variety of industries, like it is the production of resins, nylon, plastifiers, anti-oxidants, oil additives, drugs, pesticides, colorants, explosives, disinfectants and others. The disseminated discharges or effluents coming from the industrial processes toward lakes and rivers are causing a growing adverse effect in the environment, as well as a risk for the health. Numerous studies exist on the phenols removal and phenols substituted for very varied techniques, among them they are the adsorption in activated carbon. This finishes it has been used successfully for the treatment of residual waters municipal and industrial and of drinking waters and it is considered as the best technique available to eliminate organic compounds not biodegradable and toxic present in aqueous solution (US EPA, 1991). However a little information exists on studies carried out in aqueous systems with more of a phenolic compound. The activated carbon is broadly used as adsorbent due to its superficial properties in the so much treatment of water as of aqueous wastes, adsorbent for the removal of organic pollutants. The main objective of this work is the adsorption of a aqueous mixture of phenol-4 chloro phenol of different concentrations in activated carbon of mineral origin of different meshes and to diminish with it their presence in water. The experiments were carried out for lots, in normal conditions of temperature and pressure. The experimental results show that the removal capacity depends so much of the superficial properties of the sorbent like of the physical properties and chemical of the sorbate. The isotherms were carried

  18. Carbon dioxide emissions from international air freight

    Science.gov (United States)

    Howitt, Oliver J. A.; Carruthers, Michael A.; Smith, Inga J.; Rodger, Craig J.

    2011-12-01

    Greenhouse gas emissions from international air transport were excluded from reduction targets under the Kyoto Protocol, partly because of difficulties with quantifying and apportioning such emissions. Although there has been a great deal of recent research into calculating emissions from aeroplane operations globally, publicly available emissions factors for air freight emissions are scarce. This paper presents a methodology to calculate the amount of fuel burnt and the resulting CO 2 emissions from New Zealand's internationally air freighted imports and exports in 2007. This methodology could be applied to other nations and/or regions. Using data on fuel uplift, air freight and air craft movements, and assumptions on mean passenger loadings and the mass of passengers and air freight, CO 2 emissions factors of 0.82 kg CO 2 per t-km and 0.69 kg CO 2 per t-km for short-haul and long-haul journeys, respectively, were calculated. The total amount of fuel consumed for the international air transport of New Zealand's imports and exports was calculated to be 0.21 Mt and 0.17 Mt respectively, with corresponding CO 2 emissions of 0.67 Mt and 0.53 Mt.

  19. Ultrafast Scavenging of the Precursor of H(•) Atom, (e(-), H3O(+)), in Aqueous Solutions.

    Science.gov (United States)

    Balcerzyk, Anna; Schmidhammer, Uli; Wang, Furong; de la Lande, Aurélien; Mostafavi, Mehran

    2016-09-01

    Picosecond pulse radiolysis measurements have been performed in several highly concentrated HClO4 and H3PO4 aqueous solutions containing silver ions at different concentrations. Silver ion reduction is used to unravel the ultrafast reduction reactions observed at the end of a 7 ps electron pulse. Solvated electrons and silver atoms are observed by the pulse (electron beam)-probe (supercontinuum light) method. In highly acidic solutions, ultrafast reduction of silver ions is observed, a finding that is not compatible with a reaction between the H(•) atom and silver ions, which is known to be thermally activated. In addition, silver ion reduction is found to be even more efficient in phosphoric acid solution than that in neutral solution. In the acidic solutions investigated here, the species responsible for the reduction of silver atoms is considered to be the precursor of the H(•) atom. This precursor, denoted (e(-), H3O(+)), is a pair constituting an electron (not fully solvated) and H3O(+). Its structure differs from that of the pair of a solvated electron and a hydronium ion (es(-), H3O(+)), which absorbs in the visible region. The (e(-), H3O(+)) pair , called the pre-H(•) atom here, undergoes ultrafast electron transfer and can, like the presolvated electron, reduce silver ions much faster than the H(•) atom. Moreover, it is found that with the same concentration of H3O(+) the reduction reaction is favored in the phosphoric acid solution compared to that in the perchloric acid solution because of the less-efficient electron solvation process. The kinetics show that among the three reducing species, (e(-), H3O(+)), (es(-), H3O(+)), and H(•) atom, the first one is the most efficient. PMID:27472160

  20. Glucose-Derived Porous Carbon-Coated Silicon Nanowires as Efficient Electrodes for Aqueous Micro-Supercapacitors.

    Science.gov (United States)

    Devarapalli, Rami Reddy; Szunerits, Sabine; Coffinier, Yannick; Shelke, Manjusha V; Boukherroub, Rabah

    2016-02-24

    In this study, we report on carbon coating of vertically aligned silicon nanowire (SiNWs) arrays via a simple hydrothermal process using glucose as carbon precursor. Using this process, a thin carbon layer is uniformly deposited on the SiNWs. Under optimized conditions, the coated SiNWs electrode showed better electrochemical energy storage capacity as well as exceptional stability in aqueous system as compared to uncoated SiNWs. The as-measured capacitance reached 25.64 mF/cm(2) with a good stability up to 25000 charging/discharging cycles in 1 M Na2SO4 aqueous solution. PMID:26866275

  1. Kinetics of absorption of carbon dioxide into aqueous potassium salt of proline

    DEFF Research Database (Denmark)

    Paul, Subham; Thomsen, Kaj

    2012-01-01

    with KPr for the above mentioned concentration and temperature range. Following the reaction mechanism of CO2 with primary and secondary alkanolamies, the reaction of CO2 with KPr is also described using zwitterionic mechanism. Based on the pseudo-first-order condition for the CO2 absorption, the......The absorption of carbon dioxide (CO2) into aqueous solution of potassium prolinate (KPr) are studied at 303, 313, and 323K within the salt concentration range of 0.5–3.0kmolm−3 using a wetted wall column absorber. The experimental results are used to interpret the kinetics of the reaction of CO2...

  2. Mercury Removal from Aqueous Solution and Flue Gas by Adsorption on Activated Carbon Fibres

    OpenAIRE

    Nabais, Joao; Carrott, Peter; Ribeiro Carrott, Manuela

    2006-01-01

    The use of two activated carbon fibres, one laboratorial sample prepared from a commercial acrylic textile fibre and one commercial sample of Kynol1, as prepared/received and modified by reaction with powdered sulfur and H2S gas in order to increase the sulfur content were studied for the removal of mercury from aqueous solution and from flue gases from a fluidized bed combustor. The sulfur introduced ranged from 1 to 6 wt.% depending on the method used. The most important parameter ...

  3. Trace enrichment with activated carbon and determination of Ni, Hg, Sn and Cd using diethyldithiocarbamate as complexant by atomic emission spectrography (AES)

    International Nuclear Information System (INIS)

    A methods has been developed for the preconcentration and determination of trace amounts of Hg, Ni, Sn and Cd in aqueous solutions. The complexes of these elements with sodium diethyl dithiocarbamate were adsorbed on activated charcoal and determined by atomic emission spectrography d-c arc technique. Factors which affect the quantitative recovery of the microamounts of the elements were optimised. Pd was used as an internal standard. The detection limits ranged from 0.01 to 0.05 ppm. (author)

  4. Combining international cap-and-trade with national carbon taxes

    OpenAIRE

    Heindl, Peter; Wood, Peter J.; Jotzo, Frank

    2014-01-01

    This paper examines the effects of combining an international cap-and-trade scheme with national carbon taxes. We consider a two-country stochastic partial equilibrium model with log-normally distributed uncertainty. The situation is analogous to the situation where European countries impose national carbon taxes in addition to the EU emissions trading. The allowance price in the joint cap-and-trade scheme depends on the tax rate, the relative size of countries and abatement options, the magn...

  5. Combining International Cap-and-Trade with National Carbon Taxes

    OpenAIRE

    Heindl, Peter; Wood, Peter J.; Jotzo, Frank

    2014-01-01

    This paper examines the effects of combining an international cap-and-trade scheme with national carbon taxes. We consider a two-country stochastic partial equilibrium model with log-normally distributed uncertainty. The situation is analogous to the situation where European countries impose national carbon taxes in addition to the EU emissions trading. The allowance price in the joint cap-and-trade scheme depends on the tax rate, the relative size of countries and abatement op...

  6. Precipitation of calcium carbonate in aqueous solutions in presence of ethylene glycol and dodecane.

    Science.gov (United States)

    Natsi, Panagiota D.; Rokidi, Stamatia; Koutsoukos, Petros G.

    2015-04-01

    The formation of calcium carbonate (CaCO3) in aqueous supersaturated solutions has been intensively studied over the past decades, because of its significance for a number of processes of industrial and environmental interest. In the oil and gas production industry the deposition of calcium carbonate affects adversely the productivity of the wells. Calcium carbonate scale deposits formation causes serious problems in water desalination, CO2 sequestration in subsoil wells, in geothermal systems and in heat exchangers because of the low thermal coefficient of the salt. Amelioration of the operational conditions is possible only when the mechanisms underlying nucleation and crystal growth of calcium carbonate in the aqueous fluids is clarified. Given the fact that in oil production processes water miscible and immiscible hydrocarbons are present the changes of the dielectric constant of the fluid phase has serious impact in the kinetics of calcium carbonate precipitation, which remains largely unknown. The problem becomes even more complicated if polymorphism exhibited by calcium carbonate is also taken into consideration. In the present work, the stability of aqueous solutions supersaturated with respect to all calcium carbonate polymorphs and the subsequent kinetics of calcium carbonate precipitation were measured. The measurements included aqueous solutions and solutions in the presence of water miscible (ethylene glycol, MEG) and water immiscible organics (n-dodecane). All measurements were done at conditions of sustained supersaturation using the glass/ Ag/AgCl combination electrode as a probe of the precipitation and pH as the master variable for the addition of titrant solutions with appropriate concentration needed to maintenance the solution supersaturation. Initially, the metastable zone width was determined from measurements of the effect of the solution supersaturation on the induction time preceding the onset of precipitation at free-drift conditions. The

  7. 76 FR 58049 - Atomic Safety and Licensing Board; Honeywell International, Inc.; Metropolis Works Uranium...

    Science.gov (United States)

    2011-09-19

    ... From the Federal Register Online via the Government Publishing Office NUCLEAR REGULATORY COMMISSION Atomic Safety and Licensing Board; Honeywell International, Inc.; Metropolis Works Uranium... assurance for its Metropolis Works uranium conversion facility in Metropolis, Illinois. \\1\\ LBP-11-19,...

  8. International bulletin on atomic and molecular data for fusion. No. 53

    International Nuclear Information System (INIS)

    The International Bulletin on Atomic and Molecular Data for Fusion is presented in four parts: 1) The Atomic and Molecular Data Information System (AMDIS) of the IAEA; 2) the indexed papers listed separately for structure and spectra, atomic and molecular collisions, and surface interactions; 3) all bibliographic data for both the indexed and non-indexed references; 4) the Author Index refers to the bibliographic references contained in Part 3

  9. Site specific atomic polarizabilities in endohedral fullerenes and carbon onions

    International Nuclear Information System (INIS)

    We investigate the polarizability of trimetallic nitride endohedral fullerenes by partitioning the total polarizability into site specific components. This analysis indicates that the polarizability of the endohedral fullerene is essentially due to the outer fullerene cage and has insignificant contribution from the encapsulated unit. Thus, the outer fullerene cages effectively shield the encapsulated clusters and behave like Faraday cages. The polarizability of endohedral fullerenes is slightly smaller than the polarizability of the corresponding bare carbon fullerenes. The application of the site specific polarizabilities to C60@C240 and C60@C180 onions shows that, compared to the polarizability of isolated C60 fullerene, the encapsulation of the C60 in C240 and C180 fullerenes reduces its polarizability by 75% and 83%, respectively. The differences in the polarizability of C60 in the two onions is a result of differences in the bonding (intershell electron transfer), fullerene shell relaxations, and intershell separations. The site specific analysis further shows that the outer atoms in a fullerene shell contribute most to the fullerene polarizability

  10. Site specific atomic polarizabilities in endohedral fullerenes and carbon onions

    Energy Technology Data Exchange (ETDEWEB)

    Zope, Rajendra R., E-mail: rzope@utep.edu; Baruah, Tunna [Department of Physics, The University of Texas at El Paso, El Paso, Texas 79958 (United States); Computational Science Program, The University of Texas at El Paso, El Paso, Texas 79958 (United States); Bhusal, Shusil; Basurto, Luis [Department of Physics, The University of Texas at El Paso, El Paso, Texas 79958 (United States); Jackson, Koblar [Physics Department and Science of Advanced Materials Ph.D. Program, Central Michigan University, Mt. Pleasant, Michigan 48859 (United States)

    2015-08-28

    We investigate the polarizability of trimetallic nitride endohedral fullerenes by partitioning the total polarizability into site specific components. This analysis indicates that the polarizability of the endohedral fullerene is essentially due to the outer fullerene cage and has insignificant contribution from the encapsulated unit. Thus, the outer fullerene cages effectively shield the encapsulated clusters and behave like Faraday cages. The polarizability of endohedral fullerenes is slightly smaller than the polarizability of the corresponding bare carbon fullerenes. The application of the site specific polarizabilities to C{sub 60}@C{sub 240} and C{sub 60}@C{sub 180} onions shows that, compared to the polarizability of isolated C{sub 60} fullerene, the encapsulation of the C{sub 60} in C{sub 240} and C{sub 180} fullerenes reduces its polarizability by 75% and 83%, respectively. The differences in the polarizability of C{sub 60} in the two onions is a result of differences in the bonding (intershell electron transfer), fullerene shell relaxations, and intershell separations. The site specific analysis further shows that the outer atoms in a fullerene shell contribute most to the fullerene polarizability.

  11. 12th international hot atom chemistry symposium, Balatonfuered, Hungary, 23-28 September 1984. Abstracts

    International Nuclear Information System (INIS)

    This proceedings contains the abstracts of 91 papers presented at the symposium. The majority of papers discusses various hot atom reactions and decay processes. A list of previous 11 international hot atom chemistry symposia from 1959 to 1982 is also given. One paper published in full length presents an overview of them (A.P. Wolf p. 89-89/b). (R.P.)

  12. Supercritical aqueous fluids in subduction zones carrying carbon and sulfur: oxidants for the mantle wedge?

    Science.gov (United States)

    Sverjensky, Dimitri; Manning, Craig

    2014-05-01

    Much speculation surrounds the nature of aqueous fluids in subduction zones. Aqueous fluids likely trigger partial melting in the mantle wedge, influencing the chemistry of the magmas that erupt in island arcs. They also may play a role in transporting elements that could metasomatize and oxidize the overlying mantle wedge, most importantly C, S and Fe. However, full coupling of aqueous fluid chemistry with the silicate, carbonate, C, sulfide and sulfate minerals has remained limited to pressures of 0.5 GPa because of limitations on the HKF aqueous ion equation of state. Recent progress in developing a Deep Earth Water model (Sverjensky et al., 2014), calibrated with new experimental data, now enables a detailed evaluation of the evolution of aqueous fluid chemistry to a pressure of 6 GPa, well into subduction zone conditions. We report aqueous speciation models for eclogitic aqueous fluids constrained by model mineral assemblages that give preliminary indications of the solubilities of elements that could contribute to mass transfer and redox changes in the mantle wedge. For example, at 600 °C and 2.5 GPa, an aqueous fluid in equilibrium with jadeite, paragonite, muscovite, quartz, lawsonite, almandine, talc, magnesite and pyrite at QFM oxidation state with 0.1 molal total Cl, contains 5.5 molal C, 0.04 molal S, and 9 micromolal Fe. The fluid has a pH of 4.7, much greater than the neutral pH of 3.3; the predominant species and molalities are CO2 (5.0), Na+ (0.44), Si(OH)4 (0.36), HCO3- (0.26), H3SiO4- (0.23), CaHCO3+ (0.18), silica dimer (0.10), Cl- (0.09), K+ (0.08), HCOO- (0.06), H2S (0.03). Calculations for model eclogitic fluids at the higher pressures and temperatures of subarc conditions also show that the solubility of C is much greater than either S or Fe at QFM. However, in subarc eclogitic fluids of higher oxidation state (QFM +3 to +4) in equilibrium with hematite, anhydrite, jadeite, kyanite, phlogopite, coesite, lawsonite, almandine-pyrope, and

  13. Carbon Fiber Reinforced Carbon Composites Rotary Valves for Internal Combustion Engines

    Science.gov (United States)

    Northam, G. Burton (Inventor); Ransone, Philip O. (Inventor); Rivers, H. Kevin (Inventor)

    1999-01-01

    Carbon fiber reinforced carbon composite rotary, sleeve, and disc valves for internal combustion engines and the like are disclosed. The valves are formed from knitted or braided or warp-locked carbon fiber shapes. Also disclosed are valves fabricated from woven carbon fibers and from molded carbon matrix material. The valves of the present invention with their very low coefficient of thermal expansion and excellent thermal and self-lubrication properties, do not present the sealing and lubrication problems that have prevented rotary, sleeve, and disc valves from operating efficiently and reliably in the past. Also disclosed are a sealing tang to further improve sealing capabilities and anti-oxidation treatments.

  14. Carbon Fiber Reinforced Carbon Composite Rotary Valve for an Internal Combustion Engine

    Science.gov (United States)

    Northam, G.Burton (Inventor); Ransone, Philip O. (Inventor); Rivers, H. Kevin (Inventor)

    2000-01-01

    Carbon fiber reinforced carbon composite rotary sleeve, and disc valves for internal combustion engines and the like are disclosed. The valves are formed from knitted or braided or wrap-locked carbon fiber shapes. Also disclosed are valves fabricated from woven carbon fibers and from molded carbon matrix material. The valves of the present invention with their very low coefficient of thermal expansion and excellent thermal and self-lubrication properties do not present the sealing and lubrication problems that have prevented rotary sleeve and disc valves from operating efficiently and reliably in the past. Also disclosed are a sealing tang to further improve sealing capabilities and anti-oxidation treatments.

  15. Detection and Quantized Conductance of Neutral Atoms Near a Charged Carbon Nanotube

    OpenAIRE

    Ristroph, Trygve; Goodsell, Anne; Golovchenko, Jene Andrew; Hau, Lene V.

    2005-01-01

    We describe a novel single atom detector that uses the high electric field surrounding a charged single-walled carbon nanotube to attract and subsequently field-ionize neutral atoms. A theoretical study of the field-ionization tunneling rates for atomic trajectories in the attractive potential near a nanowire shows that a broadly applicable, high spatial resolution, low-power, neutral-atom detector with nearly 100% efficiency is realizable with present-day technology. Calculations also show t...

  16. Physical and electrochemical characteristics of supercapacitors based on carbide derived carbon electrodes in aqueous electrolytes

    Science.gov (United States)

    Eskusson, Jaanus; Jänes, Alar; Kikas, Arvo; Matisen, Leonard; Lust, Enn

    FIB-SEM, XPS and gas adsorption methods have been used for the characterisation of physical properties of microporous carbide derived carbon electrodes prepared from Mo 2C at 600 °C (noted as CDC-Mo 2C). Cyclic voltammetry, constant current charge/discharge, and electrochemical impedance spectroscopy have been applied to establish the electrochemical characteristics for supercapacitors consisting of the 1 M Na 2SO 4, KOH, tetraethyl ammonium iodide or 6 M KOH aqueous electrolyte and CDC-Mo 2C electrodes. The N 2 sorption values obtained have been correlated with electrochemical characteristics for supercapacitors in various aqueous electrolytes. The maximum gravimetric energy, E max, and gravimetric power, P max, for supercapacitors (taking into consideration the active material weight) have been obtained at cell voltage 0.9 V for 6 M KOH aqueous supercapacitor (E max = 5.7 Wh kg -1 and P max = 43 kW kg -1). For 1 M TEAI based SC somewhat higher E max (6.2 Wh kg -1) and comparatively low P max (7.0 kW kg -1) have been calculated.

  17. Nickel catalysts for internal reforming in molten carbonate fuel cells

    OpenAIRE

    Berger, R.J.; Doesburg, E.B.M.; Ommen, van, B.; Ross, J.R.H.

    1996-01-01

    Natural gas may be used instead of hydrogen as fuel for the molten carbonate fuel cell (MCFC) by steam reforming the natural gas inside the MCFC, using a nickel catalyst (internal reforming). The severe conditions inside the MCFC, however, require that the catalyst has a very high stability. In order to find suitable types of nickel catalysts and to obtain more knowledge about the deactivation mechanism(s) occurring during internal reforming, a series of nickel catalysts was prepared and subj...

  18. International mobility in carbon dioxide emissions

    International Nuclear Information System (INIS)

    In this paper, we analyse the evolution of international mobility in per capita CO2 emissions for the period 1971–2007. This concept reveals the distribution's degree of entrenchment which is fundamentally different from other distribution concepts. In particular, we use several different synthetic mobility measures in order to capture the various perceptions of mobility proposed in the literature. This approach can be seen as complementary to the dynamics of distribution approach. The empirical analysis yields the following main results. First, the evolution observed varies according to the mobility index used. Second, when broader mobility indices are used, the most recent years analysed (i.e. 2000–2007) and the 1970s appear to be the most dynamic periods. Third, their decomposition reveals the major role played by the non-high income countries group. Fourth, the calculation of fictitious indices associated with the three major decomposition components of general mobility indicates that exchange (i.e. changes in position) and dispersion (i.e. distribution effects) have typically been the most important mobility factors. Finally, there does not seem to be a clear, convincing relationship between mobility and the evolution of inequality, which to a certain extent underscores the need to carry out a differential analysis for mobility. The results obtained have some implications in terms of analysis and environmental policy. - Highlights: ► The evolution of international mobility in per capita CO2 emissions for the period 1971–2007 is analysed. ► Several different synthetic mobility measures are used for capturing the various perceptions of mobility. ► The mobility is high and, in a significant way, without impact on distribution. ► There does not seem to be a clear, convincing relationship between mobility and the evolution of inequality. ► The results obtained have some implications in terms of analysis and environmental policy

  19. Biosorption Studies for the Removal of Malachite Green from its Aqueous Solution by Activated Carbon Prepared from Cassava Peel

    OpenAIRE

    Parvathi, C.; Maruthavanan, T.; S. Sivamani; Prakash, C

    2011-01-01

    The association of dyes with health related problems is not a new phenomenon. The effectiveness of carbon adsorption for dye removal from textile effluent has made it an ideal alternative to other expensive treatment methods. The preparation of activated carbon from agricultural waste could increase economic return and reduce pollution. Cassava peel has been used as a raw material to produce activated carbon. The study investigates the removal of malachite green dye from its aqueous solution....

  20. Removal of insecticide carbofuran from aqueous solutions by banana stalks activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Salman, J.M. [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Hameed, B.H., E-mail: chbassim@eng.usm.my [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia)

    2010-04-15

    In this work, activated carbon was prepared from banana stalks (BSAC) waste to remove the insecticide carbofuran from aqueous solutions. The effects of contact time, initial carbofuran concentration, solution pH and temperature (30, 40 and 50 deg. C) were investigated. Adsorption isotherm, kinetics and thermodynamics of carbofuran on BSAC were studied. Equilibrium data were fitted to the Langmuir, Freundlich and Temkin isotherm models and the data best represented by the Langmuir isotherm. Thermodynamic parameters such as standard enthalpy ({Delta}H{sup o}), standard entropy ({Delta}S{sup o}) and standard free energy ({Delta}G{sup o}) were evaluated. Regeneration efficiency of spent BSAC was studied using ethanol as a solvent. The efficiency was found to be in the range of 96.97-97.35%. The results indicated that the BSAC has good regeneration and reusability characteristics and can be used as alternative to present commercial activated carbon.

  1. Enabling aqueous binders for lithium battery cathodes - Carbon coating of aluminum current collector

    Science.gov (United States)

    Doberdò, Italo; Löffler, Nicholas; Laszczynski, Nina; Cericola, Dario; Penazzi, Nerino; Bodoardo, Silvia; Kim, Guk-Tae; Passerini, Stefano

    2014-02-01

    In this manuscript a novel approach to enable aqueous binders for lithium ion battery (LIB) cathodes is reported. Producing LiNi1/3Mn1/3Co1/3O2 (NMC) electrodes using sodium-carboxymethylcellulose (CMC) as a binder and water as a solvent, in fact, results in serious aluminum corrosion during electrode manufacturing due to the high pH of the slurry. In order to prevent the direct contact of the corrosive slurry with aluminum foil, the latter is first coated with a thin carbon layer. The CMC-based electrodes formed on carbon coated aluminum foil show enhanced performance than those made using unprotected aluminum instead. In particular, electrodes using protected aluminum foil are able to deliver a capacity of 126 mAh g-1 at 1C rate, which is rather close to that delivered by polyvinylidene-di-fluoride (PVdF)-based electrode having the same composition.

  2. A Review of Spectral Methods for Dispersion Characterization of Carbon Nanotubes in Aqueous Suspensions

    Directory of Open Access Journals (Sweden)

    Jidraph Njuguna

    2015-01-01

    Full Text Available Characterization is a crucial step in the study of properties of nanomaterials to evaluate their full potential in applications. Carbon nanotube-based materials have properties that are sensitive to size, shape, concentration, and agglomeration state. It is therefore critical to quantitatively characterize these factors in situ, while the processing takes place. Traditional characterization techniques that rely on microscopy are often time consuming and in most cases provide qualitative results. Spectroscopy has been studied as an alternative tool for identifying, characterizing, and studying these materials in situ and in a quantitative way. In this paper, we provide a critical review of the spectroscopy techniques used to explore the surface properties (e.g., dispersion characteristics of carbon nanotubes in aqueous suspensions during the sonication process.

  3. RICE BRAN CARBON: AN ALTERNATIVE TO COMMERCIAL ACTIVATED CARBON FOR THE REMOVAL OF HEXAVALENT CHROMIUM FROM AQUEOUS SOLUTION

    Directory of Open Access Journals (Sweden)

    Syed Hadi Hasan

    2010-06-01

    Full Text Available Rice bran carbon (RBC prepared from rice bran (an agricultural waste was successfully utilized for the removal of hexavalent chromium from aqueous solution. The potentiality of RBC was tested and compared with commercial activated carbon (CAC, and it was found that RBC removed 95% of hexavalent chromium at pH 2, 1000 µM Cr(VI concentration, temperature 30 oC, and adsorbent dose of 2 g/L. The maximum uptake of total chromium obtained by applying the Langmuir isotherm model was 138.88 mg/g for RBC, which was found comparable to that obtained by utilizing CAC (116.28 mg/g at 40 oC. The removal of Cr(VI was found maximum at a proton to chromium ratio of 10 and chromium to carbon ratio of 0.052, and these ratios were found to be applicable over a range of Cr(VI concentrations. The removal of Cr(VI, at low pH (< 2.0, was not only due to sorption of Cr(VI but also because of reduction of Cr(VI into less toxic Cr(III, which was also adsorbed on the surface of the sorbent. The rate of reduction removal of Cr(VI followed pseudo-first order kinetics, whereas the sorption of total chromium followed pseudo-second order kinetics for both the types of activated carbons.

  4. Laser direct writing of crystalline Fe2O3 atomic sheets on steel surface in aqueous medium

    International Nuclear Information System (INIS)

    Graphical abstract: This study describes a fast and scalable synthesis of few atomic layers thin iron oxide sheets in aqueous medium with pulsed laser irradiation. We systematically studied the effects of laser parameters on synthesized nanostructures to understand the growth mechanisms. We found high density of star shaped nanostructures and large sheets of few atomic layer thicknesses are typically observed in laser assisted synthesis while small platelets are obtained when laser is not applied. Nanocomposites of iron oxide nanosheets with graphene oxide were obtained and their adsorption capability for Rhodamine B molecules was investigated. Enhanced contact area between iron oxide sheets and graphene oxide, as observed in our experimental investigation would find many applications in photocatalysis, water purification and many other emerging applications. Schematic diagram for iron oxide nanostructures formed in aqueous medium (a) without and (b) with laser exposure. (a) shows porous nanostripes and (b) shows two different morphologies of nanostructures at bottom and in liquid medium. - Abstract: In this article, pulsed laser exposure on steel surface in aqueous medium was employed to achieve fast and scalable synthesis of highly dense iron oxide nanosheets. The growth mechanisms of this unique 2D nanocrystals have been studied systematically. The effects of laser processing conditions on growth of the 2D nanocrystals have been investigated. NanoStars and nanoflakes with different densities have been observed under various laser treatment conditions. It is noteworthy that laser acts as a catalyst for growth of iron oxide nanosheet. Nanocomposites of iron oxide nanosheets with graphene oxide (GO) were obtained and their adsorption capability for Rhodamine B molecules was investigated. The enhanced contact area between iron oxide sheets and graphene oxide, as observed in our experimental investigation would find applications in catalysis, water purification and

  5. Materials Properties at Internal Interfaces: Fundamental Atomic Issues

    Energy Technology Data Exchange (ETDEWEB)

    Browning, Nigel

    2014-09-12

    During the course of this research, the microscopy methods were applied to many different systems (see publication list). However, the work can be broadly classified into three main areas: the statistical distribution of grain boundary structures under different doping conditions, the identification of individual dopant atoms in oxide materials, and the evaluation of nucleation and growth processes in liquid and more recently. The main results from each of these efforts will be discussed in the final report.

  6. Process of Energetic Carbon Atom Deposition on Si (001) Substrate by Molecular Dynamics Simulation

    Institute of Scientific and Technical Information of China (English)

    于威; 滕晓云; 李晓苇; 傅广生

    2002-01-01

    The process of energetic C atom deposition on Si (001)-(2×1) is studied by the molecular dynamics method using the semi-empirical many-bond Tersoff potential. It is found that the incident energy of the carbon atom has an important effect on the collision process and its diffusion process on the substrate. Most of the incident energy of the carbon atom is transferred to the substrate atoms within the initial two vibration periods of substrate atoms and its value increases with the incident energy. The spreading distance and penetration depth of the incident atom increasing with the incident energy are also identified. The simulated results imply that an important effect of energy of incident carbon on the film growth at Iow substrate temperature provides activation energy for silicon carbide formation through the vibration enhancement of local substrate atoms. In addition, suppressing carbon atom inhomogeneous collection and dispensing with the silicon diffusion process may be effectively promoted by the spreading and penetration of the energetic carbon atom in the silicon substrate.

  7. Adsorption of cadmium from aqueous solutions on sulfurized activated carbon prepared from nut shells

    Energy Technology Data Exchange (ETDEWEB)

    Fouladi Tajar, Amir [Chemical Engineering Department, Amirkabir University of Technology, No.424, Hafez Avenue, P.O. Box 15875-4413, Tehran (Iran, Islamic Republic of); Kaghazchi, Tahereh, E-mail: kaghazch@aut.ac.ir [Chemical Engineering Department, Amirkabir University of Technology, No.424, Hafez Avenue, P.O. Box 15875-4413, Tehran (Iran, Islamic Republic of); Soleimani, Mansooreh [Chemical Engineering Department, Amirkabir University of Technology, No.424, Hafez Avenue, P.O. Box 15875-4413, Tehran (Iran, Islamic Republic of)

    2009-06-15

    Low-cost activated carbon, derived from nut shells, and its modified sample have been used as replacements for the current expensive methods of removing cadmium from aqueous solutions and waste waters. Adsorption of cadmium onto four kinds of activated carbons has been studied; prepared activated carbon (PAC), commercial activated carbon (CAC), and the sulfurized ones (SPAC and SCAC). The activated carbon has been derived, characterized, treated with sulfur and then utilized for the removal of Cd{sup 2+}. Sulfurizing agent (SO{sub 2} gas) was successfully used in adsorbents' modification process at the ambient temperature. Samples were then characterized and tested as adsorbents of cadmium. Effect of some parameters such as contact time, initial concentration and pH were examined. With increasing pH, the adsorption of cadmium ions was increased and maximum removal, 92.4% for SPAC, was observed in pH > 8.0 (C{sub 0} = 100 mg/L). The H-type adsorption isotherms, obtained for the adsorbents, indicated a favorable process. Adsorption data on both prepared and commercial activated carbon, before and after sulfurization, followed both the Frendlich and Langmuir models. They were better fitted by Frendlich isotherm as compared to Langmuir. The maximum adsorption capacities were 90.09, 104.17, 126.58 and 142.86 mg/g for CAC, PAC, SCAC and SPAC, respectively. Accordingly, surface modification of activated carbons using SO{sub 2} greatly enhanced cadmium removal. The reversibility of the process has been studied in a qualitative manner and it shows that the spent SPAC can be effectively regenerated for further use easily.

  8. Adsorption of cadmium from aqueous solutions on sulfurized activated carbon prepared from nut shells

    International Nuclear Information System (INIS)

    Low-cost activated carbon, derived from nut shells, and its modified sample have been used as replacements for the current expensive methods of removing cadmium from aqueous solutions and waste waters. Adsorption of cadmium onto four kinds of activated carbons has been studied; prepared activated carbon (PAC), commercial activated carbon (CAC), and the sulfurized ones (SPAC and SCAC). The activated carbon has been derived, characterized, treated with sulfur and then utilized for the removal of Cd2+. Sulfurizing agent (SO2 gas) was successfully used in adsorbents' modification process at the ambient temperature. Samples were then characterized and tested as adsorbents of cadmium. Effect of some parameters such as contact time, initial concentration and pH were examined. With increasing pH, the adsorption of cadmium ions was increased and maximum removal, 92.4% for SPAC, was observed in pH > 8.0 (C0 = 100 mg/L). The H-type adsorption isotherms, obtained for the adsorbents, indicated a favorable process. Adsorption data on both prepared and commercial activated carbon, before and after sulfurization, followed both the Frendlich and Langmuir models. They were better fitted by Frendlich isotherm as compared to Langmuir. The maximum adsorption capacities were 90.09, 104.17, 126.58 and 142.86 mg/g for CAC, PAC, SCAC and SPAC, respectively. Accordingly, surface modification of activated carbons using SO2 greatly enhanced cadmium removal. The reversibility of the process has been studied in a qualitative manner and it shows that the spent SPAC can be effectively regenerated for further use easily.

  9. Aqueous phase adsorption of different sized molecules on activated carbon fibers: Effect of textural properties.

    Science.gov (United States)

    Prajapati, Yogendra N; Bhaduri, Bhaskar; Joshi, Harish C; Srivastava, Anurag; Verma, Nishith

    2016-07-01

    The effect that the textural properties of rayon-based activated carbon fibers (ACFs), such as the BET surface area and pore size distribution (PSD), have on the adsorption of differently sized molecules, namely, brilliant yellow (BY), methyl orange (MO) and phenol (PH), was investigated in the aqueous phase. ACF samples with different BET areas and PSDs were produced by steam-activating carbonized fibers for different activation times (0.25, 0.5, and 1 h). The samples activated for 0.25 h were predominantly microporous, whereas those activated for relatively longer times contained hierarchical micro-mesopores. The adsorption capacities of the ACFs for the adsorbate increased with increasing BET surface area and pore volume, and ranged from 51 to 1306 mg/g depending on the textural properties of the ACFs and adsorbate size. The adsorption capacities of the hierarchical ACF samples followed the order BY > MO > PH. Interestingly, the number of molecules adsorbed by the ACFs followed the reverse order: PH > MO > BY. This anomaly was attributed to the increasing molecular weight of the PH, MO and BY molecules. The equilibrium adsorption data were described using the Langmuir isotherm. This study shows that suitable textural modifications to ACFs are required for the efficient aqueous phase removal of an adsorbate. PMID:27107386

  10. Olivine alteration and H2 production in carbonate-rich, low temperature aqueous environments

    Science.gov (United States)

    Neubeck, Anna; Duc, Nguyen Thanh; Hellevang, Helge; Oze, Christopher; Bastviken, David; Bacsik, Zoltán; Holm, Nils G.

    2014-06-01

    Hydrous alteration of olivine is capable of producing molecular hydrogen (H2) under a wide variety of hydrothermal conditions. Although olivine hydrolysis (i.e., serpentinization) has commonly been assessed at elevated temperatures (>100 °C), the nature of these reactions in relation to H2 production at lower temperatures has not been systematically evaluated, especially with regard to carbonate-rich fluids. Specifically, carbonate formation may kinetically infringe on geochemical routes related to serpentinization and H2 production at lower temperatures. Here time-dependent interactions of solid, liquid, and gaseous phases with respect to olivine hydrolysis in a carbonate-rich solution (20 mM HCO3-) at 30, 50 and 70 °C for 315 days is investigated experimentally. Within the first two months, amorphous Si-rich (i.e., talc-like) and carbonate phases precipitated; however, no inhibition of olivine dissolution is observed at any temperature based on surface chemistry analyses. High-resolution surface analyses confirm that precipitates grew as spheroids or vertically to form topographic highs allowing further dissolution of the free olivine surfaces and exposing potential catalysts. Despite no magnetite (Fe3O4) being detected, H2 increased with time in experiments carried out at 70 °C, indicating an alternative coupled route for Fe oxidation and H2 production. Spectrophotometry analyses show that aqueous Fe(II) is largely converted to Fe(III) potentially integrating into other phases such as serpentine and talc, thus providing a viable pathway for H2 production. No increase in H2 production was observed in experiments carried out at 30 and 50 °C supporting observations that incorporation of Fe(II) into carbonates occurred faster than the intertwined processes of olivine hydrolysis and Fe(III) oxidation. Overall, carbonate formation is confirmed to be a major influence related to H2 production in low-temperature serpentinization systems. We studied low temperature

  11. Carbon-13 NMR characterization of actinyl(VI) carbonate complexes in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Clark, D.L.; Hobart, D.E.; Palmer, P.D. [Los Alamos National Lab., NM (United States); Sullivan, J.C. [Argonne National Lab., IL (United States); Stout, B.E. [Cincinnati Univ., OH (United States). Dept. of Chemistry

    1992-07-01

    The uranyl(VI) carbonate system has been re-examined using {sup 13}C NMR of 99.9% {sup 13}C-enriched U{sup VI}O{sub 2} ({sup 13}CO{sub 3}){sub 3}{sup 4{minus}} in millimolar concentrations. By careful control of carbonate ion concentration, we have confirmed the existence of the trimer, and observed dynamic equilibrium between the monomer and the timer. In addition, the ligand exchange reaction between free and coordinated carbonate on Pu{sup VI}O{sub 2}({sup 13}CO{sub 3}){sub 3}{sup 4{minus}} and Am{sup VI}O{sub 2}({sup 13}CO{sub 3}){sub 3}{sup 4{minus}} systems has been examined by variable temperature {sup 13}C NMR line-broadening techniques {sup 13}C NMR line-broadening techniques. A modified Carr-Purcell-Meiboom-Gill NMR pulse sequence was written to allow for experimental determination of ligand exchange parameters for paramagnetic actinide complexes. Preliminary Eyring analysis has provided activation parameters of {Delta}G{sup {double_dagger}}{sub 295} = 56 kJ/M, {Delta}H{sup {double_dagger}} = 38 kJ/M, and {Delta}S{sup {double_dagger}} = {minus}60 J/M-K for the plutonyl triscarbonate system, suggesting an associative transition state for the plutonyl (VI) carbonate complex self-exchange reaction. Experiments for determination of the activation parameters for the americium (VI) carbonate system are in progress.

  12. Determination of molybdenum in silicates through atomic absorption spectrometry using pre-concentration by active carbon

    International Nuclear Information System (INIS)

    An analytical procedure for molybdenum determination in geological materials through Atomic Absorption Spectrometry, after pre-concentration of the Mo-APDC complex in activated carbon, has been developed, which is needed in order to reduce the dilution effect in the sample decomposition. During the development of this method the influence of pH, the amount of APDC for complexation of Mo and the interference of Fe, Ca, Mn, Al, K, Na, Mg and Ti were tested. It was shown that none of these causes any significant effect on the Mo determination proposed. The results of the analysis at the international geochemical reference samples JB-1 (basalt) and GH (granite) were very accurate and showed that the detection limit in rocks (1,00g) is 0,6 ppm, when using sample dilution of 1 ml and microinjection techniques. (author)

  13. Pulse electrodeposition of Pt and Pt–Ru methanol-oxidation nanocatalysts onto carbon nanotubes in citric acid aqueous solutions

    International Nuclear Information System (INIS)

    In this study, platinum nanoparticle/carbon nanotube (Pt NP/CNT) and platinum–ruthenium nanoparticle (Pt–Ru NP/CNT) hybrid nanocatalysts were prepared by the pulse-electrodeposition method in different aqueous solutions containing citric acid (CA) or sulfuric acid (SA). The electrocatalytic properties of the Pt NP/CNT and Pt–Ru NP/CNT electrodes prepared using different aqueous solutions were investigated for methanol oxidation. The results show that the electrochemical mass activities of these hybrid nanocatalysts prepared in the CA aqueous solution were increased by factors of 1.46 and 2.77 for Pt NPs and Pt–Ru NPs, respectively, compared with those prepared in SA aqueous solutions using the same procedure. These increased mass activities are attributed to the CA playing dual roles as both a stabilizing agent and a particle size reducing agent in the aqueous solutions. The approach developed in this work enables further reductions in the particle sizes of noble-metal nanocatalysts. - Highlights: • Pulse-electrodeposition of Pt or Pt–Ru nanoparticles on carbon nanotubes • Carbon nanotubes used as a catalyst-supporting material • Citric acid used as reducing agent in the aqueous electrodeposition solutions • Electrochemical activity for methanol oxidation improved by a factor of 1.46 to 2.77

  14. International bulletin on atomic and molecular data for fusion. No. 54-55

    International Nuclear Information System (INIS)

    This bulletin is published by the International Atomic Energy Agency to provide atomic and molecular data relevant to fusion research and technology. In the first part the indexed papers are listed separately for (i) structure and spectra (energy levels, wavelengths, transition probabilities, oscillator strengths, polarizabilities, electric moments, interatomic potentials), (ii) atomic and molecular collisions (photon collisions, electron collisions, heavy-particle collisions), and (iii) surface interactions (sputtering, chemical reactions, trapping and detrapping, adsorption, desorption, reflection, and secondary electron emission). There are also chapters with beam-matter interactions and data on interactions of atomic particles with fields. In the second Part contains the bibliographic data, essentially for the above listed topics

  15. Temperature dependence of the internal dynamics of a protein in an aqueous solvent: Decoupling from the solvent viscosity

    International Nuclear Information System (INIS)

    Highlights: ► LiCl enables low-temperature proteins studies in aqueous solutions without freezing. ► Glass transition temperature of aqueous solvent is unaffected by lithium chloride. ► Solvent viscosity governs global dynamics of lysozyme down to glass transition arrest. ► Lysozyme internal dynamics is decoupled showing dynamic arrest at higher temperatures. - Abstract: We have recently observed decoupling of the dynamics of a protein from its aqueous solvent [Chu et al., JPCL 3 (2012) 380]; here we report the more detailed studies. We analyzed quasielastic neutron scattering data from a 40 mg/ml solution of lysozyme in (D2O)8(LiCl) and (H2O)8(LiCl). The internal dynamics of lysozyme exhibited super-Arrhenius temperature dependence with no crossover to a different regime down to at least 200 K. The decoupling of the internal protein dynamics from the viscosity of its aqueous solvent is evident. The temperature dependence of the protein dynamics indicates an apparent dynamic arrest at a temperature above 190 K, whereas the glass transition temperature for the solvent is around 135–140 K. The internal dynamics of the solvated protein is coupled to the dynamics of its hydration shell, not of the bulk solvent, which is qualitatively altered by the salt to defer the dynamic arrest to 135–140 K

  16. Role of the surface chemistry of activated carbons in dye removal from aqueous solution

    Science.gov (United States)

    Zhou, Hua-lei; Zhen, Wen-juan; Zhu, Qian; Wu, Xiao-bin; Chang, Zhi-dong; Li, Wen-jun

    2015-07-01

    Commercial activated carbons were modified by a series of chemical or physical treatments using H2O2, NH3, and heating under N2 flow without notably changing their pore structures. The resultant carbons were characterized by N2 adsorption and Bohem titration and then used to remove Ponceau 4R, methyl orange and brilliant blue from aqueous solutions. Surface chemistry was found to play a significantly different role in removing these three compounds. The removal of anionic Ponceau 4R increases with increasing carbon surface basicity due to the predominant dispersive interaction mechanism. In contrast, surface chemistry has little effect on the removal of anionic methyl orange, which can be explained by two parallel mechanisms involving electrostatic and dispersive interactions due to the basic amine group in a dye molecule. The influence of surface chemistry on the removal of amphoteric brilliant blue dye can also be ignored due to a weak interaction between the carbons and dye molecules, which is resulted from strong cohesive energy from electrostatic forces inside amphoteric dye molecules.

  17. Ultradry Carbon Dioxide-in-Water Foams with Viscoelastic Aqueous Phases.

    Science.gov (United States)

    Xue, Zheng; Worthen, Andrew J; Da, Chang; Qajar, Ali; Ketchum, Isaiah Robert; Alzobaidi, Shehab; Huh, Chun; Prodanović, Maša; Johnston, Keith P

    2016-01-12

    For foams with ultra low water contents, the capillary pressure is very large and induces rapid drainage that destabilizes the aqueous lamellae between the gas bubbles. However, we show that high-pressure CO2-in-water foams can be stabilized with a viscoelastic aqueous phase composed of entangled wormlike micelles, even for extremely high CO2 volume fractions ϕ of 0.95 to 0.98; the viscosity of these ultradry foams increased by up to 3-4-fold, reaching more than 100 cP relative to foams formed with conventional low viscosity aqueous phases. The foam morphology consisted of fine ∼20 μm polyhedral-shaped CO2 bubbles that were stable for hours. The wormlike micelles were formed by mixing anionic sodium lauryl ether sulfate (SLES) with salt and a protonated cationic surfactant, as shown by cryogenic transmission electron microscopy (cryo-TEM) and large values of the zero-shear viscosity and the dynamic storage and loss moduli. With the highly viscous continuous aqueous phases, the foam lamella drainage rates were low, as corroborated by confocal microscopy. The preservation of viscous thick lamellae resulted in lower rates of Ostwald ripening relative to conventional foams as shown by high-pressure optical microscopy. The ability to stabilize viscous ultra high internal phase foams is expected to find utility in various practical applications, including nearly "waterless" fracturing fluids for recovery of oil and gas in shale, offering the possibility of a massive reduction in the amount of wastewater. PMID:26666311

  18. Mineral sequestration of CO2 by aqueous carbonation of coal combustion fly-ash

    International Nuclear Information System (INIS)

    The increasing CO2 concentration in the Earth's atmosphere, mainly caused by fossil fuel combustion, has led to concerns about global warming. A technology that could possibly contribute to reducing carbon dioxide emissions is the in-situ mineral sequestration (long term geological storage) or the ex-situ mineral sequestration (controlled industrial reactors) of CO2. In the present study, we propose to use coal combustion fly-ash, an industrial waste that contains about 4.1 wt.% of lime (CaO), to sequester carbon dioxide by aqueous carbonation. The carbonation reaction was carried out in two successive chemical reactions, first, the irreversible hydration of lime. CaO + H2O → Ca(OH)2 second, the spontaneous carbonation of calcium hydroxide suspension. Ca(OH)2 + CO2 → CaCO3 + H2O A significant CaO-CaCO3 chemical transformation (approximately 82% of carbonation efficiency) was estimated by pressure-mass balance after 2 h of reaction at 30 deg. C. In addition, the qualitative comparison of X-ray diffraction spectra for reactants and products revealed a complete CaO-CaCO3 conversion. The carbonation efficiency of CaO was independent on the initial pressure of CO2 (10, 20, 30 and 40 bar) and it was not significantly affected by reaction temperature (room temperature '20-25', 30 and 60 deg. C) and by fly-ash dose (50, 100, 150 g). The kinetic data demonstrated that the initial rate of CO2 transfer was enhanced by carbonation process for our experiments. The precipitate calcium carbonate was characterized by isolated micrometric particles and micrometric agglomerates of calcite (SEM observations). Finally, the geochemical modelling using PHREEQC software indicated that the final solutions (i.e. after reaction) are supersaturated with respect to calcium carbonate (0.7 ≤ saturation index ≤ 1.1). This experimental study demonstrates that 1 ton of fly-ash could sequester up to 26 kg of CO2, i.e. 38.18 ton of fly-ash per ton of CO2 sequestered. This confirms the

  19. Electrochemical activation of carbon cloth in aqueous inorganic salt solution for superior capacitive performance

    Science.gov (United States)

    Ye, Dong; Yu, Yao; Tang, Jie; Liu, Lin; Wu, Yue

    2016-05-01

    Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as an electrode material for flexible supercapacitors. However, pristine CC has such a low surface area and poor electrochemical activity that the energy storage capability is usually very poor. Herein, we report a green method, two-step electrochemical activation in an aqueous solution of inorganic salts, to significantly enhance the capacitance of CC for supercapacitor application. Micro-cracks, exfoliated carbon fiber shells, and oxygen-containing functional groups (OFGs) were introduced onto the surface of the carbon filament. This resulted in an enhancement of over two orders of magnitude in capacitance compared to that of the bare CC electrode, reaching up to a maximum areal capacitance of 505.5 mF cm-2 at the current density of 6 mA cm-2 in aqueous H2SO4 electrolyte. Electrochemical reduction of CC electrodes led to the removal of most electrochemically unstable surface OFGs, resulting in superior charging/discharging rate capability and excellent cycling stability. Although the activated CC electrode contained a high-level of surface oxygen functional groups (~15 at%), it still exhibited a remarkable charging-discharging rate capability, retaining ~88% of the capacitance when the charging rate increased from 6 to 48 mA cm-2. Moreover, the activated CC electrode exhibited excellent cycling stability with ~97% capacitance remaining after 10 000 cycles at a current density of 24 mA cm-2. A symmetrical supercapacitor based on the activated CC exhibited an ideal capacitive behavior and fast charge-discharge properties. Such a simple, environment-friendly, and cost-effective strategy to activate CC shows great potential in the fabrication of high-performance flexible supercapacitors.Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as

  20. The influence of atomizer internal design and liquid physical properties on effervescent atomizing of coal-water slurry

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Meng; Duan, Yufeng [Southeast Univ., Nanjing (China). Inst. of Thermal Engineering

    2013-07-01

    This study investigated the dependence of effervescent atomizing of coal-water slurry (CWS) on atomizer internal design and fluid properties. Results demonstrate that internal design of atomizer and fluid properties directly affect the two-phase flow pattern inside the atomizer which consequently affects the spray quality. The influence of mixing chamber length on spray quality is not significant at the ALR of 0.15 except for spray 0.75 glycerol/0.248 water/0.002 xanthan mixture. The same trend also found in the effect of angle of aeration holes at ALR of 0.15. Large diameter of the inclined aeration holes shows small SMD for water. The consistency index of fluids has no effect on the spray quality and Sauter Mean Diameter (SMD) increases when polymer additions were added to the glycerin-water mixture. The radial profile of SMD for spray water are almost flat, however, the largest SMD can be obtained at the edge of spray for three other fluids.

  1. Electrochemical activation of carbon cloth in aqueous inorganic salt solution for superior capacitive performance.

    Science.gov (United States)

    Ye, Dong; Yu, Yao; Tang, Jie; Liu, Lin; Wu, Yue

    2016-05-21

    Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as an electrode material for flexible supercapacitors. However, pristine CC has such a low surface area and poor electrochemical activity that the energy storage capability is usually very poor. Herein, we report a green method, two-step electrochemical activation in an aqueous solution of inorganic salts, to significantly enhance the capacitance of CC for supercapacitor application. Micro-cracks, exfoliated carbon fiber shells, and oxygen-containing functional groups (OFGs) were introduced onto the surface of the carbon filament. This resulted in an enhancement of over two orders of magnitude in capacitance compared to that of the bare CC electrode, reaching up to a maximum areal capacitance of 505.5 mF cm(-2) at the current density of 6 mA cm(-2) in aqueous H2SO4 electrolyte. Electrochemical reduction of CC electrodes led to the removal of most electrochemically unstable surface OFGs, resulting in superior charging/discharging rate capability and excellent cycling stability. Although the activated CC electrode contained a high-level of surface oxygen functional groups (∼15 at%), it still exhibited a remarkable charging-discharging rate capability, retaining ∼88% of the capacitance when the charging rate increased from 6 to 48 mA cm(-2). Moreover, the activated CC electrode exhibited excellent cycling stability with ∼97% capacitance remaining after 10 000 cycles at a current density of 24 mA cm(-2). A symmetrical supercapacitor based on the activated CC exhibited an ideal capacitive behavior and fast charge-discharge properties. Such a simple, environment-friendly, and cost-effective strategy to activate CC shows great potential in the fabrication of high-performance flexible supercapacitors. PMID:27141910

  2. Adsorption of copper, lead and cadmium from aqueous solutions by activated carbon prepared from saffron leaves

    Directory of Open Access Journals (Sweden)

    Shidvash Dowlatshahi

    2014-11-01

    Full Text Available Background: Industrial development has caused the release of various pollutants including heavy metals into the environment. These toxic compounds are extremely dangerous to living beings and the environment due to their non-biodegradability, severe toxicity, carcinogenicity, the ability to be accumulated in nature and the ability to contaminate groundwater and surface water. The aim of the present research was to provide an appropriate and cost-effective adsorbent to remove heavy metals from aqueous solutions. Methods: The activated carbon was produced from the dried. Batch experiments were performed on real and synthetic samples at room temperature. The effect of pH, adsorbent dose, initial concentration, and contact time were studied, and the adsorption isotherms of heavy metals were determined. The removal efficiency was evaluated on real wastewater. Results: The maximum removal efficiency of heavy metals (copper, cadmium and lead by activated carbon adsorbent prepared from saffron leaves was obtained in pH 7. The optimum amount of adsorbent was 0.6 g, and the optimum contact times were 45 min for copper and cadmium ions and 90 min for lead ion, respectively. In these optimum conditions the removal efficiencies were 76.36%, 91.25% and 97.5%, respectively. The removal efficiencies of heavy metals from actual samples (copper industry and the battery industry in the optimum conditions were 82.25%, 69.95% and 91.23%, respectively. The results obtained showed the highest correlation with Langmuir isotherm model. Conclusion: Based on the results obtained, the activated carbon produced from saffron leaves has a good capability in removal of the metal ions from the aqueous solutions. Considering the availability of saffron leaves in Khorasan, its cost-effectiveness, and high uptake capacity, it can be applied as a proper absorbent to remove the heavy metals from industrial wastewater.

  3. Safeguarding the atom. The IAEA and international nuclear affairs

    International Nuclear Information System (INIS)

    Paper is concerned with progress attained in recent years in the area of non-proliferation and disarmament which depend on effective verification system i.e. safeguards. The IAEA safeguards system has been strengthened in many ways since since 1991. It is acknowledged to be a credible means by which the international community can be assured that nuclear material and facilities are being used exclusively for peaceful purposes. Challenges that still remain are reviewed in preparation for the forthcoming NPT Review conference

  4. The International Atomic Energy Agency: activities and relationship with Mexico

    International Nuclear Information System (INIS)

    Legal and political studies on the activities of the IAEA infer that the pacific uses of nuclear energy become more significant every day in the ambit of international relationships. The studies analyze as a whole relationships among member states. The first part is divided into four chapters, starting with the background and creation of the agency, its structure, statutes, amendments and the performance of its main organisms. It continues to describe mechanisms and programmes carried out, including cooperation agreements between the IAEA and other specialized organizations in the United Nations. It ends up with the IAEA performance resulting from different treaties. The second part examines Mexican norms on nuclear matter as well as relationships between Mexico and the IAEA. It demonstrates that achievements in the Agency have been possible because of the establishment of an international cooperation basis, which avoids duplicity of actions. The conclusions recommend joint efforts from both the developed and the developing countries in the following: a) to imbue public opinion with the goodness of nuclear energy; b) to discourage the construction and operation of nuclear installations; c) to unify national standards on nuclear safety and control; d) to decrease export restrictions, based on safeguards; e) to promote internal nuclear research in Mexico or throught regional integration agreements, with technical assistance and support from the IAEA. (author)

  5. Synthesis and Electrochemical Properties of Al doped Lithium Manganate Powders by Spray Pyrolysis Using Carbonate Aqueous Solution

    OpenAIRE

    HIROSE, Shoji; KODERA, Takayuki; Ogihara, Takashi

    2011-01-01

    Al doped LiMn2O4 powders were prepared by spray pyrolysis using the aqueous solution ofmanganese carbonate. The aqueous solution, in which manganese carbonate was uniformly dispersedby a surfactant, was used as the starting solution. Al2O3 nanopowders, Al(OH)3 and Al(NO3)3·9H2Owere used as the doping agent of Al. A scanning electron microscope photograph showed that Aldoped LiMn2O4 powders had spherical morphology with broad particle size distribution. X-raydiffraction revealed that crystal p...

  6. Method of removal of metal atoms and explosives from aqueous solution using suspended plant cells

    International Nuclear Information System (INIS)

    The use of plant suspension cultures to remove ionic metallic species and TNT-based explosives and their oxidation products from aqueous solution is described. Several plant strains were investigated including D. innoxia, Citrus citrus, and Black Mexican Sweet Corn. All showed significant ability to remove metal ions. Ions removed to sub-ppm levels include barium, iron, and plutonium. D. innoxia cells growing in media containing weapons effluent contaminated with Ba2+ also remove TNT, other explosives and oxidation products thereof from solution. The use of dead, dehydrated cells were also found to be use in treating waste directly. (author)

  7. The internal consistency of the North Sea carbonate system

    Science.gov (United States)

    Salt, Lesley A.; Thomas, Helmuth; Bozec, Yann; Borges, Alberto V.; de Baar, Hein J. W.

    2016-05-01

    In 2002 (February) and 2005 (August), the full suite of carbonate system parameters (total alkalinity (AT), dissolved inorganic carbon (DIC), pH, and partial pressure of CO2 (pCO2) were measured on two re-occupations of the entire North Sea basin, with three parameters (AT, DIC, pCO2) measured on four additional re-occupations, covering all four seasons, allowing an assessment of the internal consistency of the carbonate system. For most of the year, there is a similar level of internal consistency, with AT being calculated to within ± 6 μmol kg- 1 using DIC and pH, DIC to ± 6 μmol kg- 1 using AT and pH, pH to ± 0.008 using AT and pCO2, and pCO2 to ± 8 μatm using DIC and pH, with the dissociation constants of Millero et al. (2006). In spring, however, we observe a significant decline in the ability to accurately calculate the carbonate system. Lower consistency is observed with an increasing fraction of Baltic Sea water, caused by the high contribution of organic alkalinity in this water mass, not accounted for in the carbonate system calculations. Attempts to improve the internal consistency by accounting for the unconventional salinity-borate relationships in freshwater and the Baltic Sea, and through application of the new North Atlantic salinity-boron relationship (Lee et al., 2010), resulted in no significant difference in the internal consistency.

  8. Carbon nanotubes as tips for atomic force microscopy

    Institute of Scientific and Technical Information of China (English)

    国立秋; 徐宗伟; 赵铁强; 赵清亮; 张飞虎; 董申

    2004-01-01

    Ordinary AFM probes' characters prevent the AFM' s application in various scopes. Carbon nanotubes represent ideal AFM probe materials for their higher aspect ratio, larger Young' s modulus, unique chemical structure, and well-defined electronic property. Carbon nanotube AFM probes are obtained by using a new method of attaching carbon nanotubes to the end of ordinary AFM probes, and are then used for doing AFM experiments. These experiments indicated that carbon nanotube probes have higher elastic deformation, higher resolution and higher durability. And it was also found that carbon nanotube probes can accurately reflect the morphology of deep narrow gaps, while ordinary probes can not reflect.

  9. On the effect of aqueous Ca on magnesite growth - Insight into trace element inhibition of carbonate mineral precipitation

    Science.gov (United States)

    Berninger, Ulf-Niklas; Jordan, Guntram; Lindner, Michael; Reul, Alexander; Schott, Jacques; Oelkers, Eric H.

    2016-04-01

    Motivated by the strong effect of aqueous Mg on calcite growth rates, this study used hydrothermal atomic force microscopy (HAFM) and hydrothermal mixed-flow reactor (HMFR) experiments to explore the effect of aqueous Ca on magnesite growth kinetics at 100 °C and pH ∼7.7. Obtuse step velocities on (1 0 4) surfaces during magnesite growth were measured to be 4 ± 3 nm/s at fluid saturation states, equal to the ion activity quotient divided by the equilibrium constant for the magnesite hydrolysis reaction, of 86-117. These rates do not vary systematically with aqueous Ca concentration up to 3 × 10-3 mol/kg. Magnesite growth rates determined by HAFM are found to be negligibly affected by the presence of aqueous Ca at these saturation states and are largely consistent with those previously reported in aqueous Ca-free systems by Saldi et al. (2009) and Gautier et al. (2015). Similarly, magnesite growth rates measured by HMFR exhibit no systematic variation on aqueous Ca concentrations. Rates in this study, however, were extended to higher degrees of fluid supersaturation with respect to magnesite than previous studies. All measured HMFR rates can be accurately described taking account the combined effects of both the spiral growth and two dimensional nucleation/growth mechanisms. Despite the lack of a clear effect of aqueous Ca on magnesite growth rates, Raman spectroscopy confirmed the incorporation of up to 8 mol percent of Ca2+ into the growing magnesite structure.

  10. Cu determination in crude oil distillation products by atomic absorption and inductively coupled plasma mass spectrometry after analyte transfer to aqueous solution

    International Nuclear Information System (INIS)

    Cu was determined in a wide range of petroleum products from crude oil distillation using flame atomic absorption spectrometry (FAAS), electrothermal atomic absorption spectrometry (ETAAS) and inductively coupled plasma mass spectrometry (ICP-MS). Different procedures of sample preparation were evaluated: (i) mineralization with sulfuric acid in an open system (ii) mineralization in a closed microwave system (iii) combustion in hydrogen-oxygen flame in the Wickbold's apparatus (iv) matrix evaporation followed by acid dissolution, and (v) acidic extraction. All the above procedures led to the transfer of the analyte into an aqueous solution for the analytical measurement step. It was found that application of FAAS was limited to the analysis of the heaviest petroleum products of high Cu content. In ICP-MS, the use of internal reference method (with Rh or In as internal reference element) was required to eliminate the matrix effects in the analysis of extracts and the concentrated solutions of mineralized heavy petroleum products. The detection limits (in original samples) were equal to, respectively, 10, 86, 3.3, 0.9 and 0.4 ng g-1 in procedures i-v with ETAAS detection and 10, 78, 1.1 and 0.5 ng g-1 in procedures i-iii and v with ICP-MS detection. The procedures recommended here were validated by recovery experiments, certified reference materials analysis and comparison of results, obtained for a given sample, in different ways. The Cu content in the analyzed samples was: 50-110 ng g-1 in crude oil, -1 in gasoline, -1 in atmospheric oil, -1 in heavy vacuum oil and 140-300 ng g-1 in distillation residue

  11. International bulletin on atomic and molecular data for fusion. No. 46

    International Nuclear Information System (INIS)

    The bulletin is published by the International Atomic Energy Agency to provide atomic and molecular data relevant to fusion research and technology. In Part I the indexed papers are listed separately for (i) structure and spectra (energy levels, wavelengths; transition probabilities, oscillator strengths; interatomic potentials); (ii) atomic and molecular collisions (photon collisions; electron collisions; heavy-particle collisions; homonuclear sequences; isoelectronic sequences), and (iii) surface interactions (sputtering; chemical reactions; trapping and detrapping; surface damage; blistering, flaking; secondary electron emission). Part II contains the bibliographic data for the above listed topics and for high energy laser- and beam-matter interaction; interaction of atomic particles with fields. The atomic and molecular data needs in fusion research, as identified during the IAEA Consultants' Meeting on 'Atomic and Molecular Database for Hydrogen Recycling and Helium Exhaust from Fusion Reactors', June 1992, Vienna, are listed, covering (i) atomic and molecular collision processes, (ii) particle-surface interaction processes, and (iii) the status of data bases on atomic and molecular data and plasma-surface interactions. News on the ALADDIN (A labelled Atomic Data INterface) system is provided. Finally, a list of evaluated atomic and molecular data bases is provided

  12. Effects of Atomic-Scale Structure on the Fracture Properties of Amorphous Carbon - Carbon Nanotube Composites

    Science.gov (United States)

    Jensen, Benjamin D.; Wise, Kristopher E.; Odegard, Gregory M.

    2015-01-01

    The fracture of carbon materials is a complex process, the understanding of which is critical to the development of next generation high performance materials. While quantum mechanical (QM) calculations are the most accurate way to model fracture, the fracture behavior of many carbon-based composite engineering materials, such as carbon nanotube (CNT) composites, is a multi-scale process that occurs on time and length scales beyond the practical limitations of QM methods. The Reax Force Field (ReaxFF) is capable of predicting mechanical properties involving strong deformation, bond breaking and bond formation in the classical molecular dynamics framework. This has been achieved by adding to the potential energy function a bond-order term that varies continuously with distance. The use of an empirical bond order potential, such as ReaxFF, enables the simulation of failure in molecular systems that are several orders of magnitude larger than would be possible in QM techniques. In this work, the fracture behavior of an amorphous carbon (AC) matrix reinforced with CNTs was modeled using molecular dynamics with the ReaxFF reactive forcefield. Care was taken to select the appropriate simulation parameters, which can be different from those required when using traditional fixed-bond force fields. The effect of CNT arrangement was investigated with three systems: a single-wall nanotube (SWNT) array, a multi-wall nanotube (MWNT) array, and a SWNT bundle system. For each arrangement, covalent bonds are added between the CNTs and AC, with crosslink fractions ranging from 0-25% of the interfacial CNT atoms. The SWNT and MWNT array systems represent ideal cases with evenly spaced CNTs; the SWNT bundle system represents a more realistic case because, in practice, van der Waals interactions lead to the agglomeration of CNTs into bundles. The simulation results will serve as guidance in setting experimental processing conditions to optimize the mechanical properties of CNT

  13. Pb2+ adsorption from aqueous solutions on activated carbons obtained from lignocellulosic residues

    Directory of Open Access Journals (Sweden)

    L. Giraldo

    2008-03-01

    Full Text Available Activated carbons obtained from cane sugar bagasse (ACB, African palm pit (ACP and sawdust (ACS were prepared through an impregnated with HNO3 and thermal treatment in an atmosphere in N2/steam water at 1173 K. Adsorption isotherms of N2 at 77 K and of CO2 at 273 K were determined for the activated carbons for which surface area and pore volume values were from 868 to 1100 m²g-1 and from 0.27 to 0.55cm³ g-1, respectively. These results were correlated, with the ones obtained for adsorption the adsorption isotherms of Pb2+ in aqueous solutions. Impregnation of the lignocellulosic materials with nitric acid produced acid-type activated carbons with total acid site contents between 4.13 and 6.93 mmol g-1 and pH at the point of zero charge values between 2.7 and 4.1, which were within range of the adsorption, at different pH values, since they determined, the surface charge of the activated carbons. Adsorption isotherms of Pb2+ at different pH values (2-8 at 298 K were determined. The ion adsorption capacity on ACB, ACP and ACS were 13.7, 15.2 and 17.5 mg.g-1, respectively. Experimental data were fitted to the Langmuir and Freundlich models and all cases the former fit better. The highest values for the quantity adsorbed on the monolayer, qm, were at pH 4, whereas the surface, charge of activated carbons was negative and the lead species mainly present was Pb2+. For higher pHs, the quantity of Pb2+ adsorbed decreased, and this had an important effect on adsorption, the surface characteristics of the solids and the hydroxilated lead species that were formed in the system.

  14. The dynamics simulation of Ne atom injected into single-wall carbon nanotube

    International Nuclear Information System (INIS)

    The dynamical processes of Ne atom injected into single-wall carbon nanotube (SWCNT) are modeled with molecular dynamics simulations. The threshold energies to encapsulate rare-gas atoms in SWCNT are presented. The range of tube radius for stable oscillation is revealed, which is independent of the type of carbon nanotubes. And the oscillatory frequency is sensitive to the change in the diameter, the length and chirality of the tube

  15. Effect of Surface Charge on Surface-Initiated Atom Transfer Radical Polymerization from Cellulose Nanocrystals in Aqueous Media.

    Science.gov (United States)

    Zoppe, Justin O; Xu, Xingyu; Känel, Cindy; Orsolini, Paola; Siqueira, Gilberto; Tingaut, Philippe; Zimmermann, Tanja; Klok, Harm-Anton

    2016-04-11

    Cellulose nanocrystals (CNCs) with different charge densities were utilized to examine the role of electrostatic interactions on surface-initiated atom transfer radical polymerization (SI-ATRP) in aqueous media. To this end, growth of hydrophilic uncharged poly(N,N-dimethylacrylamide) (PDMAM) brushes was monitored by electrophoresis, (1)H NMR spectroscopy, and dynamic light scattering (DLS). Molecular weight and polydispersity of PDMAM brushes was determined by GPC analysis of hydrolytically cleaved polymers. Initiator and polymer brush grafting densities, and thus, initiator efficiencies were derived from elemental analysis. Higher initiator efficiency of polymer brush growth was observed for CNCs with higher anionic surface sulfate half-ester group density, but at the expense of high polydispersity caused by inefficient deactivation. PDMAM grafts with number-average molecular weights up to 530 kDa and polydispersity indices Cu-mediated SI-CRP are analogous to those conducted in solution. PMID:26901869

  16. Removal of organic contaminants from aqueous solution by cattle manure compost (CMC) derived activated carbons

    International Nuclear Information System (INIS)

    The activated carbons (ACs) prepared from cattle manure compost (CMC) with various pore structure and surface chemistry were used to remove phenol and methylene blue (MB) from aqueous solutions. The adsorption equilibrium and kinetics of two organic contaminants onto the ACs were investigated and the schematic models for the adsorptive processes were proposed. The result shows that the removal of functional groups from ACs surface leads to decreasing both rate constants for phenol and MB adsorption. It also causes the decrement of MB adsorption capacity. However, the decrease of surface functional groups was found to result in the increase of phenol adsorption capacity. In our schematic model for adsorptive processes, the presence of acidic functional groups on the surface of carbon is assumed to act as channels for diffusion of adsorbate molecules onto small pores, therefore, promotes the adsorption rate of both phenol and MB. In phenol solution, water molecules firstly adsorb on surface oxygen groups by H-bonding and subsequently form water clusters, which cause partial blockage of the micropores, deduce electrons from the π-electron system of the carbon basal planes, hence, impede or prevent phenol adsorption. On the contrary, in MB solution, the oxygen groups prefer to combine with MB+ cations than water molecules, which lead to the increase of MB adsorption capacity.

  17. Lead and copper removal from aqueous solutions using carbon foam derived from phenol resin.

    Science.gov (United States)

    Lee, Chang-Gu; Jeon, Jun-Woo; Hwang, Min-Jin; Ahn, Kyu-Hong; Park, Chanhyuk; Choi, Jae-Woo; Lee, Sang-Hyup

    2015-07-01

    Phenolic resin-based carbon foam was prepared as an adsorbent for removing heavy metals from aqueous solutions. The surface of the produced carbon foam had a well-developed open cell structure and the specific surface area according to the BET model was 458.59m(2)g(-1). Batch experiments showed that removal ratio increased in the order of copper (19.83%), zinc (34.35%), cadmium (59.82%), and lead (73.99%) in mixed solutions with the same initial concentration (50mgL(-1)). The results indicated that the Sips isotherm model was the most suitable for describing the experimental data of lead and copper. The maximum adsorption capacity of lead and copper determined to Sips model were 491mgg(-1) and 247mgg(-1). The obtained pore diffusion coefficients for lead and copper were found to be 1.02×10(-6) and 2.42×10(-7)m(2)s(-1), respectively. Post-sorption characteristics indicated that surface precipitation was the primary mechanism of lead and copper removal by the carbon foam, while the functional groups on the surface of the foam did not affect metal adsorption. PMID:25819762

  18. Carbon nanohybrids used as catalysts and emulsifiers for reactions in biphasic aqueous/organic systems

    Institute of Scientific and Technical Information of China (English)

    Daniel E. Resasco

    2014-01-01

    This mini-review summarizes some novel aspects of reactions conducted in aqueous/organic emul-sions stabilized by carbon nanohybrids functionalized with catalytic species. Carbon nanohybrids represent a family of solid catalysts that not only can stabilize water-oil emulsions in the same fash-ion as Pickering emulsions, but also catalyze reactions at the liquid/liquid interface. Several exam-ples are discussed in this mini-review. They include (a) aldol condensation-hydrodeoxygenation tandem reactions catalyzed by basic (MgO) and metal (Pd) catalysts, respectively; (b) Fischer-Tropsch synthesis catalyzed by carbon-nanotube-supported Ru;and (c) emulsion polymerization of styrene for the production of conductive polymer composites. Conducting these reactions in emul-sion generates important advantages, such as increased liquid/liquid interfacial area that conse-quently means faster mass transfer rates of molecules between the two phases, effective separation of products from the reaction mixture by differences in the water-oil solubility, and significant changes in product selectivity that can be adjusted by modifying the emulsion characteristics.

  19. Carbon nanotubes dispersed in aqueous solution by ruthenium(ii) polypyridyl complexes.

    Science.gov (United States)

    Huang, Kewei; Saha, Avishek; Dirian, Konstantin; Jiang, Chengmin; Chu, Pin-Lei E; Tour, James M; Guldi, Dirk M; Martí, Angel A

    2016-07-21

    Cationic ruthenium(ii) polypyridyl complexes with appended pyrene groups have been synthesized and used to disperse single-walled carbon nanotubes (SWCNT) in aqueous solutions. To this end, planar pyrene groups enable association by means of π-stacking onto carbon nanotubes and, in turn, the attachment of the cationic ruthenium complexes. Importantly, the ionic nature of the ruthenium complexes allows the formation of stable dispersions featuring individualized SWCNTs in water as confirmed in a number of spectroscopic and microscopic assays. In addition, steady-state photoluminescence spectroscopy was used to probe the excited state interactions between the ruthenium complexes and SWCNTs. These studies show that the photoluminescence of both, that is, of the ruthenium complexes and of SWCNTs, are quenched when they interact with each other. Pump-probe transient absorption experiments were performed to shed light onto the nature of the photoluminescence quenching, showing carbon nanotube-based bands with picosecond lifetimes, but no new bands which could be unambigously assigned to photoinduced charge transfer process. Thus, from the spectroscopic data, we conclude that quenching of the photoluminescence of the ruthenium complexes is due to energy transfer to proximal SWCNTs. PMID:27353007

  20. Optimizing the electrochemical performance of aqueous symmetric supercapacitors based on an activated carbon xerogel

    Science.gov (United States)

    Calvo, E. G.; Lufrano, F.; Staiti, P.; Brigandì, A.; Arenillas, A.; Menéndez, J. A.

    2013-11-01

    A highly porous carbon xerogel was synthesized by means of physical activation. The activated carbon xerogel, which displayed a well-developed porous texture (micro- and meso-porosity), was employed as electrode material in different supercapacitors. In assessing the performance of the supercapacitors, special attention was paid to their dimensions and the type of electrolyte used. Both the method of electrode manufacture (rolling and punching of 1 cm2 pellets vs. casting by means of a film applicator to produce 4 cm2 electrodes) and the type of supercapacitor (Swagelok (R) system vs. cell with graphite plate current collectors) were evaluated. The results reveal that the cells with larger electrodes were able to store higher amounts of energy. In addition to the cells, the electrochemical characteristics in aqueous electrolytes with a different pH were studied (H2SO4, Na2SO4 and KOH, 1 M). The highest capacitance values were achieved with sulphuric acid (196 F g-1 as opposed to 140 and 106 F g-1 for Na2SO4 and KOH, respectively), probably due to its higher ionic conductivity and the basic nature of the oxygen functionalities found on the surface of the carbon xerogel. Nevertheless, because of the corrosive character of sulphuric acid, Na2SO4 would be a more suitable electrolyte.

  1. Sorption of lanthanum and erbium from aqueous solution by activated carbon prepared from rice husk

    International Nuclear Information System (INIS)

    A biomass agricultural waste material, rice husk (RH) was used for preparation of activated carbon by chemical activation using phosphoric acid. The effect of various factors, e.g. time, ph, initial concentration and temperature of carbon on the adsorption capacity of lanthanum and erbium were quantitatively determined. It was found that the monolayer capacity is 175.4 mg/g for La(III) and 250 mg/g for Er(III) . The calculated activation energy of La(III) adsorption on the activated carbon derived from rice husk was equal to 5.84 kJ/ mol while 14.6 kJ/ mol for Er(III), which confirm that the reaction is mainly particle-diffusion controlled. The kinetics of sorption was described by a model of a pseudo-second-order. External diffusion and intra-particular diffusion were examined. The experimental data show that the external diffusion and intra-particular diffusion are significant in the determination of the sorption rate. Therefore, the developed sorbent is considered as a better replacement technology for removal of La (III) and Er(III) ions from aqueous solution due to its low cost and good efficiency, fast kinetics, as well as easy to handle and thus no or small amount of secondary sludge is obtained in this application

  2. Structure and stability of a silicon cluster on sequential doping with carbon atoms

    Science.gov (United States)

    AzeezullaNazrulla, Mohammed; Joshi, Krati; Israel, S.; Krishnamurty, Sailaja

    2016-02-01

    SiC is a highly stable material in bulk. On the other hand, alloys of silicon and carbon at nanoscale length are interesting from both technological as well fundamental view point and are being currently synthesized by various experimental groups (Truong et. al., 2015 [26]). In the present work, we identify a well-known silicon cluster viz., Si10 and dope it sequentially with carbon atoms. The evolution of electronic structure (spin state and the structural properties) on doping, the charge redistribution and structural properties are analyzed. It is interesting to note that the ground state SiC clusters prefer to be in the lowest spin state. Further, it is seen that carbon atoms are the electron rich centres while silicon atoms are electron deficient in every SiC alloy cluster. The carbon-carbon bond lengths in alloy clusters are equivalent to those seen in fullerene molecules. Interestingly, the carbon atoms tend to aggregate together with silicon atoms surrounding them by donating the charge. As a consequence, very few Si-Si bonds are noted with increasing concentrations of C atoms in a SiC alloy. Physical and chemical stability of doped clusters is studied by carrying out finite temperature behaviour and adsorbing O2 molecule on Si9C and Si8C2 clusters, respectively.

  3. Adsorption of tetracycline from aqueous solutions onto multi-walled carbon nanotubes with different oxygen contents

    Science.gov (United States)

    Yu, Fei; Ma, Jie; Han, Sheng

    2014-06-01

    Oxidized multi-walled carbon nanotubes (MWCNTs) with different oxygen contents were investigated for the adsorption of tetracycline (TC) from aqueous solutions. As the surface oxygen content of the MWCNTs increased, the maximum adsorption capacity and adsorption coefficient of TC increased to the largest values and then decreased. The relation can be attributed to the interplay between the nanotubes' dispersibility and the water cluster formation upon TC adsorption. The overall adsorption kinetics of TC onto CNTs-3.2%O might be dependent on both intra-particle diffusion and boundary layer diffusion. The maximum adsorption capacity of TC on CNTs-3.2%O was achieved in the pH range of 3.3-8.0 due to formation of water clusters or H-bonds. Furthermore, the presence of Cu2+ could significantly enhanced TC adsorption at pH of 5.0. However, the solution ionic strength did not exhibit remarkable effect on TC adsorption. In addition, when pH is beyond the range (3.3-8.0), the electrostatic interactions caused the decrease of TC adsorption capacity. Our results indicate that surface properties and aqueous solution chemistry play important roles in TC adsorption on MWCNTs.

  4. Interaction of fragmented double-stranded DNA with carbon nanotubes in aqueous solution

    Science.gov (United States)

    Gladchenko, G. O.; Karachevtsev, M. V.; Leontiev, V. S.; Valeev, V. A.; Glamazda, A. Yu.; Plokhotnichenko, A. M.; Stepanian, S. G.

    Aqueous suspensions of ultrasonically fragmented double-stranded (fds-) DNA and single-walled carbon nanotubes (SWNTs) have been investigated by UV- and IR-absorption, NIR-emission and Raman spectroscopy. According to gel-electrophoresis, the lengths of the polymer fragments were 100-500 base pairs. Analysis of IR and UV data indicates the presence of both double-stranded (ds) and single-stranded (ss)-regions in the fragments. SWNT complex with DNA was revealed by NIR-emission and Raman spectroscopy. It turned out that fds-DNA is less efficient in holding nanotubes in the aqueous solution than ss-DNA. From the UV-data, the character of the helix-coil transition is seen to be like that for fds-DNA off and on nanotube, however, DNA thermostability increased in this latter case. The effective charge density on the DNA sugar-phosphate backbone of the fds-DNA:SWNT hybrid was less than that of DNA alone. Spectroscopic data can be explained by a model in which the formation of hybrids starts due to the interaction between untwisted ss-regions of DNA and the nanotube: the strands wrap on the tube and thus create an 'anchor' for the whole polymer. The ds-part of the polymer is located close to the nanotube.

  5. Electrochemical studies on nanometal oxide-activated carbon composite electrodes for aqueous supercapacitors

    Science.gov (United States)

    Ho, Mui Yen; Khiew, Poi Sim; Isa, Dino; Chiu, Wee Siong

    2014-11-01

    In present study, the electrochemical performance of eco-friendly and cost-effective titanium oxide (TiO2)-based and zinc oxide-based nanocomposite electrodes were studied in neutral aqueous Na2SO3 electrolyte, respectively. The electrochemical properties of these composite electrodes were studied using cyclic voltammetry (CV), galvanostatic charge-discharge (CD) and electrochemical impedance spectroscopy (EIS). The experimental results reveal that these two nanocomposite electrodes achieve the highest specific capacitance at fairly low oxide loading onto activated carbon (AC) electrodes, respectively. Considerable enhancement of the electrochemical properties of TiO2/AC and ZnO/AC nanocomposite electrodes is achieved via synergistic effects contributed from the nanostructured metal oxides and the high surface area mesoporous AC. Cations and anions from metal oxides and aqueous electrolyte such as Ti4+, Zn2+, Na+ and SO32- can occupy some pores within the high-surface-area AC electrodes, forming the electric double layer at the electrode-electrolyte interface. Additionally, both TiO2 and ZnO nanoparticles can provide favourable surface adsorption sites for SO32- anions which subsequently facilitate the faradaic processes for pseudocapacitive effect. These two systems provide the low cost material electrodes and the low environmental impact electrolyte which offer the increased charge storage without compromising charge storage kinetics.

  6. International Atomic Energy Agency Annual Report 2014 [Spanish Version

    International Nuclear Information System (INIS)

    Development Goals. Technical cooperation projects provide expertise in fields where nuclear techniques offer advantages over other approaches, or where they can successfully supplement conventional approaches. The IAEA had 342 million euros in regular budget funding in 2014, while its extrabudgetary expenditures totalled 68.3 million euros. Highlights mentioned in the Annual report include: Nuclear Energy: • The IAEA published several new guidance materials for countries considering to introduce nuclear power programmes. Four new e-learning modules on the IAEA’s ‘Milestones’ approach to nuclear power were launched, bringing to 11 the number of modules in this series available on iaea.org by the end of the year. • More systematic training approaches were used in the nuclear field globally, helping to ensure succession and knowledge management, concluded participants of the International Conference on Human Resource Development for Nuclear Power Programmes. • The International Symposium on Uranium Raw Material for the Nuclear Fuel Cycle highlighted new initiatives such as innovative financing and the use of advanced technologies in 'smart mines', and the need for increased attention to stakeholder engagement. Nuclear Sciences and Applications: • As part of the IAEA’s effort to meet growing Member State needs, the Renovation of the Nuclear Applications Laboratories (ReNuAL) project began on 1 January, 2014. Following completion of the feasibility study in February, the strategic plan for the project was issued in May, and conceptual designs for the new buildings were completed in November. A donor package providing detailed information on the project and its requirements was made available to Member States last December. • Against the background of outbreaks of avian influenza H5N1 and H7N9 and other animal diseases that can spread to humans, the IAEA established the VetLab network of animal diagnostic laboratories in Africa to intensify its work on

  7. International Atomic Energy Agency Annual Report 2014 [French Version

    International Nuclear Information System (INIS)

    Development Goals. Technical cooperation projects provide expertise in fields where nuclear techniques offer advantages over other approaches, or where they can successfully supplement conventional approaches. The IAEA had 342 million euros in regular budget funding in 2014, while its extrabudgetary expenditures totalled 68.3 million euros. Highlights mentioned in the Annual report include: Nuclear Energy: • The IAEA published several new guidance materials for countries considering to introduce nuclear power programmes. Four new e-learning modules on the IAEA’s ‘Milestones’ approach to nuclear power were launched, bringing to 11 the number of modules in this series available on iaea.org by the end of the year. • More systematic training approaches were used in the nuclear field globally, helping to ensure succession and knowledge management, concluded participants of the International Conference on Human Resource Development for Nuclear Power Programmes. • The International Symposium on Uranium Raw Material for the Nuclear Fuel Cycle highlighted new initiatives such as innovative financing and the use of advanced technologies in 'smart mines', and the need for increased attention to stakeholder engagement. Nuclear Sciences and Applications: • As part of the IAEA’s effort to meet growing Member State needs, the Renovation of the Nuclear Applications Laboratories (ReNuAL) project began on 1 January, 2014. Following completion of the feasibility study in February, the strategic plan for the project was issued in May, and conceptual designs for the new buildings were completed in November. A donor package providing detailed information on the project and its requirements was made available to Member States last December. • Against the background of outbreaks of avian influenza H5N1 and H7N9 and other animal diseases that can spread to humans, the IAEA established the VetLab network of animal diagnostic laboratories in Africa to intensify its work on

  8. International Atomic Energy Agency Annual Report 2014 [Chinese Version

    International Nuclear Information System (INIS)

    Development Goals. Technical cooperation projects provide expertise in fields where nuclear techniques offer advantages over other approaches, or where they can successfully supplement conventional approaches. The IAEA had 342 million euros in regular budget funding in 2014, while its extrabudgetary expenditures totalled 68.3 million euros. Highlights mentioned in the Annual report include: Nuclear Energy: • The IAEA published several new guidance materials for countries considering to introduce nuclear power programmes. Four new e-learning modules on the IAEA’s ‘Milestones’ approach to nuclear power were launched, bringing to 11 the number of modules in this series available on iaea.org by the end of the year. • More systematic training approaches were used in the nuclear field globally, helping to ensure succession and knowledge management, concluded participants of the International Conference on Human Resource Development for Nuclear Power Programmes. • The International Symposium on Uranium Raw Material for the Nuclear Fuel Cycle highlighted new initiatives such as innovative financing and the use of advanced technologies in 'smart mines', and the need for increased attention to stakeholder engagement. Nuclear Sciences and Applications: • As part of the IAEA’s effort to meet growing Member State needs, the Renovation of the Nuclear Applications Laboratories (ReNuAL) project began on 1 January, 2014. Following completion of the feasibility study in February, the strategic plan for the project was issued in May, and conceptual designs for the new buildings were completed in November. A donor package providing detailed information on the project and its requirements was made available to Member States last December. • Against the background of outbreaks of avian influenza H5N1 and H7N9 and other animal diseases that can spread to humans, the IAEA established the VetLab network of animal diagnostic laboratories in Africa to intensify its work on

  9. International Atomic Energy Agency Annual Report 2014 [Russian Version

    International Nuclear Information System (INIS)

    Development Goals. Technical cooperation projects provide expertise in fields where nuclear techniques offer advantages over other approaches, or where they can successfully supplement conventional approaches. The IAEA had 342 million euros in regular budget funding in 2014, while its extrabudgetary expenditures totalled 68.3 million euros. Highlights mentioned in the Annual report include: Nuclear Energy: • The IAEA published several new guidance materials for countries considering to introduce nuclear power programmes. Four new e-learning modules on the IAEA’s ‘Milestones’ approach to nuclear power were launched, bringing to 11 the number of modules in this series available on iaea.org by the end of the year. • More systematic training approaches were used in the nuclear field globally, helping to ensure succession and knowledge management, concluded participants of the International Conference on Human Resource Development for Nuclear Power Programmes. • The International Symposium on Uranium Raw Material for the Nuclear Fuel Cycle highlighted new initiatives such as innovative financing and the use of advanced technologies in 'smart mines', and the need for increased attention to stakeholder engagement. Nuclear Sciences and Applications: • As part of the IAEA’s effort to meet growing Member State needs, the Renovation of the Nuclear Applications Laboratories (ReNuAL) project began on 1 January, 2014. Following completion of the feasibility study in February, the strategic plan for the project was issued in May, and conceptual designs for the new buildings were completed in November. A donor package providing detailed information on the project and its requirements was made available to Member States last December. • Against the background of outbreaks of avian influenza H5N1 and H7N9 and other animal diseases that can spread to humans, the IAEA established the VetLab network of animal diagnostic laboratories in Africa to intensify its work on

  10. International Atomic Energy Agency Annual Report 2014 [Arabic Version

    International Nuclear Information System (INIS)

    Development Goals. Technical cooperation projects provide expertise in fields where nuclear techniques offer advantages over other approaches, or where they can successfully supplement conventional approaches. The IAEA had 342 million euros in regular budget funding in 2014, while its extrabudgetary expenditures totalled 68.3 million euros. Highlights mentioned in the Annual report include: Nuclear Energy: • The IAEA published several new guidance materials for countries considering to introduce nuclear power programmes. Four new e-learning modules on the IAEA’s ‘Milestones’ approach to nuclear power were launched, bringing to 11 the number of modules in this series available on iaea.org by the end of the year. • More systematic training approaches were used in the nuclear field globally, helping to ensure succession and knowledge management, concluded participants of the International Conference on Human Resource Development for Nuclear Power Programmes. • The International Symposium on Uranium Raw Material for the Nuclear Fuel Cycle highlighted new initiatives such as innovative financing and the use of advanced technologies in 'smart mines', and the need for increased attention to stakeholder engagement. Nuclear Sciences and Applications: • As part of the IAEA’s effort to meet growing Member State needs, the Renovation of the Nuclear Applications Laboratories (ReNuAL) project began on 1 January, 2014. Following completion of the feasibility study in February, the strategic plan for the project was issued in May, and conceptual designs for the new buildings were completed in November. A donor package providing detailed information on the project and its requirements was made available to Member States last December. • Against the background of outbreaks of avian influenza H5N1 and H7N9 and other animal diseases that can spread to humans, the IAEA established the VetLab network of animal diagnostic laboratories in Africa to intensify its work on

  11. Studies on removal of NH4+-N from aqueous solution by using the activated carbons derived from rice husk

    International Nuclear Information System (INIS)

    Water pollution caused by ammonia nitrogen has attracted a great attention as its toxicity affects both the environment and human health. The objective of this paper was to investigate the adsorption behavior of NH4+-N from aqueous solution by activated carbons prepared from rice husk. The physico-chemical properties of the activated carbon were characterized by Brunauer-Emmett-Teller (BET) test, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). It was found that the NH4+-N adsorption on the rice husk derived carbons was dependent on adsorbent dosage and solution pH. The adsorption kinetics and isotherms of NH4+-N by rice husk carbon were also investigated, and good correlation coefficients were obtained for the pseudo-second order kinetic equation. Dubinin-Radushkevitch (D-R) adsorption isotherm model could better describe the adsorption behavior of NH4+-N on the rice husk carbon. Calculated by D-R model, the adsorption course of NH4+-N on the rice husk carbon was favored chemical ion-exchange mechanism. Moreover, the activated carbon adsorbed NH4+-N was highly fertilizer conservation especially for the nitrogen element. It was proposed that the amount of removed NH4+-N from aqueous solutions would increase evidently treated by rice husk carbon if combined with biological method. -- Highlights: ► The dosage of rice husk carbon and pH affected the removal of NH4+-N from aqueous solution. ► D-R model could better describe the adsorption behavior of NH4+-N on the rice husk carbon. ► The removing of NH4+-N would be risen by rice husk carbon if combined with biological method.

  12. Computer simulation of rare-gas atoms injection into single-wall carbon nanotube

    International Nuclear Information System (INIS)

    The process of rare-gas atoms (He, Ne, Ar) injected into single-wall carbon nanotube (SWNT) was modeled with molecular-dynamics simulations. The site dependence of the threshold energy of rare-gas atoms forming endohedral complexes was investigated, and the formation mechanism of some defects was revealed. The hole on the sidewall of the SWNT induced by incident rare-gas atoms can be healed by annealing at a certain temperature

  13. Surface activated carbon nanospheres for fast adsorption of silver ions from aqueous solutions.

    Science.gov (United States)

    Song, Xianghua; Gunawan, Poernomo; Jiang, Rongrong; Leong, Susanna Su Jan; Wang, Kean; Xu, Rong

    2011-10-30

    We report the synthesis and activation of colloidal carbon nanospheres (CNS) for adsorption of Ag(I) ions from aqueous solutions. CNS (400-500 nm in diameter) was synthesized via simple hydrothermal treatment of glucose solution. The surface of nonporous CNS after being activated by NaOH was enriched with -OH and -COO(-) functional groups. Despite the low surface area (nanoparticles on the external surface of CNS. The kinetic data can be well fitted to the pseudo-second-order kinetics model. The adsorbed silver can be easily recovered by dilute acid solutions and the CNS can be reactivated by the same treatment with NaOH solution. The excellent adsorption performance and reusability have also been demonstrated in a continuous mode. The NaOH activated CNS reported here could represent a new type of low-cost and efficient adsorbent nanomaterials for removal of trace Ag(I) ions for drinking water production. PMID:21862215

  14. Adsorption of organic acids from dilute aqueous solution onto activated carbon

    International Nuclear Information System (INIS)

    The radioisotope technique was used to study the removal of organic acid contaminants from dilute aqueous solutions onto activated carbon. Acetic acid, propionic acid, n-butyric acid, n-hexanoic acid and n-heptanoic acid were studied at 278, 298, and 3130K. Three bi-solute acid mixtures (acetic and propionic acids, acetic and butanoic acids, and propionic and butanoic acids) were studied at 278 and 2980K. Isotherms of the single-solute systems were obtained at three different temperatures in the very dilute concentration region (less than 1% by weight). These data are very important in the prediction of bi-solute equilibrium data. A Polanyi-based competitive adsorption potential theory was used to predict the bi-solute equilibrium uptakes. Average errors between calculated and experimental data ranges from 4% to 14%. It was found that the competitive adsorption potential theory gives slightly better results than the ideal adsorbed solution theory

  15. Removal of uranium from drinking water and other aqueous systems using modified powdered activated carbon

    International Nuclear Information System (INIS)

    A simple, rapid and eco friendly method for removal of high concentration of Uranium (U) from ground water (>2500 ppb), Mine water(>1000 ppb) and other aqueous systems has been developed based on laboratory trials using 10 litres of mine water and ground water. The removal of uranium was greater than 95% with a contact time of 10 minutes with modified powdered activated carbon (MPAC) at the natural pH of water. The concentration of Uranium left behind in drinking water after MPAC treatment (if necessary twice) was less than 15 ppb and is below WHO/AERB permissible limits. The methodology is so simple that it could be applied at remote villages to produce uranium free drinking water at the natural pH of water

  16. Electrochemical Reduction of Carbon Monoxide in Aqueous Electrolytes at Gas Diffusion Hydrophobic Electrodes

    International Nuclear Information System (INIS)

    This paper investigates the influence of the material of the electro-catalyst, the electrode composition, the type and concentration of the electrolyte, the temperature and the potential of the electrode on the electroreduction of carbon monoxide in aqueous electrolytes. The following metal powders were used as electrocatalysts: Co, Ni, Fe, Nb, Pt, W, Cu, Cd, Pb, Zn, and Raney nickel. A large series of tests showed that no organic products were synthesized in the electroysis in the presence of CO on the metals Pt, Nb, Cd, W, Cu, Pb, and Zn. The only product in the whole potential range was hydrogen, derived from the decomposition of the electrolyte. Methane, ethane, and traces of ethylene were obtained on Ni, Co, Fe, and Raney nickel. With respect to the other hydrocarbons the methane content was equal to 95%. Best results were obtained on nickel electrodes

  17. ADSORPTION OF COPPER FROM AQUEOUS SOLUTION BY ELAIS GUINEENSIS KERNEL ACTIVATED CARBON

    Directory of Open Access Journals (Sweden)

    NAJUA DELAILA TUMIN

    2008-08-01

    Full Text Available In this study, a series of batch laboratory experiments were conducted in order to investigate the feasibility of Elais Guineensis kernel or known as palm kernel shell (PKS-based activated carbon for the removal of copper from aqueous solution by the adsorption process. Investigation was carried out by studying the influence of initial solution pH, adsorbent dosage and initial concentration of copper. The particle size of PKS used was categorized as PKS–M. All batch experiments were carried out at a constant temperature of 30°C (±2°C using mechanical shaker that operated at 100 rpm. The single component equilibrium data was analyzed using Langmuir, Freundlich, Redlich-Peterson, Temkin and Toth adsorption isotherms.

  18. Adsorption of a textile dye from aqueous solutions by carbon nanotubes

    International Nuclear Information System (INIS)

    Multi-walled and single-walled carbon nanotubes were used as adsorbents for the removal of Reactive Blue 4 textile dye from aqueous solutions. The adsorbents were characterised using Raman spectroscopy, N2 adsorption/desorption isotherms and scanning and transmission electron microscopy. The effects of pH, agitation time and temperature on adsorption capacity were studied. In the acidic pH region, the adsorption of the dye was favourable using both adsorbents. The contact time to obtain equilibrium isotherms at 298-323 K was fixed at 4 hours for both adsorbents. For Reactive Blue 4 dye, Liu isotherm model gave the best fit for the equilibrium data. The maximum sorption capacity for adsorption of the dye occurred at 323 K, attaining values of 502.5 and 567.7 mg g-1 for MWCNT and SWCNT, respectively. (author)

  19. Kinetic adsorption of application of carbon nanotubes for Pb(II) removal from aqueous solution

    Institute of Scientific and Technical Information of China (English)

    Nassereldeen A Kabbashi; Muataz A Atieh; Abdullah Al-Mamun; Mohamed E S Mirghami; MD Z Alam; Noorahayu Yahya

    2009-01-01

    The capability of carbon nanotubes (CNTs) to adsorb lead (Pb) in aqueous solution was investigated. Batch mode adsorption experiment was conducted to determine the effects of pH, agitation speed, CNTs dosage and contact time. The removal of Pb(II) was reach to maximum value 85% or 83% at pH 5 or 40 mg/L of CNTs, respectively. Higher correlation coefficients from Langmuir isotherm model indicates the strong adsorptions of Pb(II) on the surface of CNTs (adsorption capacity Xm = 102.04 mg/g). From this study, the results indicates that the highest percentage removal of Pb (96.03%) can be achieved at pH 5, 40 mg/L of CNTs, contact time 80 min, and agitation speed 50 r/min.

  20. The accuracy and limitations of a new meter used to measure aqueous carbon dioxide

    DEFF Research Database (Denmark)

    Moran, Damian; Tirsgård, Bjørn; Steffensen, John F.

    2010-01-01

    The OxyGuard CO2 Analyzer is a novel meter that can directly measure aqueous CO2 gas pressure using a water-resistant gas-permeable membrane and infra-red absorption cell. The pCO2 is converted to a concentration via a solubility factor determined from the calibration procedure and a thermistor. We...... undertook to independently validate the precision and utility of this meter. Water flow over the probe membrane was a key determinant of the reaction time. At water velocities of ≥30 cm s−1 the time to 99% span was 6–7 min, while at 0 cm s−1 it was 55–60 min. Temperature and CO2(aq) concentration did...... where accurate pH and carbonate alkalinity determinations are difficult to obtain, such as saline waters and waters of high organic loadings....

  1. Carbon dioxide assist for non-aqueous sodium–oxygen batteries

    KAUST Repository

    Das, Shyamal K.

    2013-02-01

    We report a novel non-aqueous Na-air battery that utilizes a gas mixture of CO2 and O2. The battery exhibits a high specific energy of 6500-7000 Whkg- 1 (based on the carbon mass) over a range of CO2 feed compositions. The energy density achieved is higher, by 200% to 300%, than that obtained in pure oxygen. Ex-situ FTIR and XRD analysis reveal that Na2O2, Na2C2O 4 and Na2CO3 are the principal discharge products. The Na-CO2/O2 and Mg-CO2/O 2 battery platforms provide a promising, new approach for CO 2 capture and generation of electrical energy. © 2012 Elsevier B.V. All rights reserved.

  2. Molecular dynamics investigation of carbon nanotube junctions in non-aqueous solutions

    KAUST Repository

    Gkionis, Konstantinos

    2014-07-23

    The properties of liquids in a confined environment are known to differ from those in the bulk. Extending this knowledge to geometries defined by two metallic layers in contact with the ends of a carbon nanotube is important for describing a large class of nanodevices that operate in non-aqueous environments. Here we report a series of classical molecular dynamics simulations for gold-electrode junctions in acetone, cyclohexane and N,N-dimethylformamide solutions and analyze the structure and the dynamics of the solvents in different regions of the nanojunction. The presence of the nanotube has little effect on the ordering of the solvents along its axis, while in the transversal direction deviations are observed. Importantly, the orientational dynamics of the solvents at the electrode-nanotube interface differ dramatically from that found when only the electrodes are present.

  3. Adsorptive removal of congo red dye from aqueous solution using bael shell carbon

    International Nuclear Information System (INIS)

    This study investigates the potential use of bael shell carbon (BSC) as an adsorbent for the removal of congo red (CR) dye from aqueous solution. The effect of various operational parameters such as contact time, temperature, pH, and dye concentration were studied. The adsorption kinetics was modeled by first-order reversible kinetics, pseudo-first-order kinetics, and pseudo-second-order kinetics. The dye uptake process obeyed the pseudo-second-order kinetic expression at pH 5.7, 7 and 8 whereas the pseudo-first-order kinetic model was fitted well at pH 9. Langmuir, Freundlich and Temkin adsorption models were applied to fit adsorption equilibrium data. The best-fitted data was obtained with the Freundlich model. Thermodynamic study showed that adsorption of CR onto BSC was endothermic in nature and favorable with the positive ΔHo value of 13.613 kJ/mol.

  4. Removal of dyes from aqueous solutions using activated carbon prepared from rice husk residue.

    Science.gov (United States)

    Li, Yaxin; Zhang, Xian; Yang, Ruiguang; Li, Guiying; Hu, Changwei

    2016-01-01

    The treatment of dye wastewater by activated carbon (AC) prepared from rice husk residue wastes was studied. Batch adsorption studies were conducted to investigate the effects of contact time, initial concentration (50-450 mg/L), pH (3-11) and temperature (30-70 °C) on the removal of methylene blue (MB), neutral red, and methyl orange. Kinetic investigation revealed that the adsorption of dyes followed pseudo-second-order kinetics. The results suggested that AC was effective to remove dyes, especially MB, from aqueous solutions. Desorption studies found that chemisorption by the adsorbent might be the major mode of dye removal. Fourier transform infrared results suggested that dye molecules were likely to combine with the O-H and P=OOH groups of AC. PMID:26942535

  5. Adsorption of a textile dye from aqueous solutions by carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Machado, Fernando M.; Bergmann, Carlos P., E-mail: fernando.machado@hotmail.com.br [Universidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS (Brazil). Dept. de Materiais; Lima, Eder C.; Adebayo, Matthew A. [Universidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS (Brazil). Inst. de Quimica; Fagan, Solange B. [Centro Universitario Franciscano (UNIFRA), Santa Maria, RS (Brazil). Area de Ciencias Tecnologicas

    2014-08-15

    Multi-walled and single-walled carbon nanotubes were used as adsorbents for the removal of Reactive Blue 4 textile dye from aqueous solutions. The adsorbents were characterised using Raman spectroscopy, N{sub 2} adsorption/desorption isotherms and scanning and transmission electron microscopy. The effects of pH, agitation time and temperature on adsorption capacity were studied. In the acidic pH region, the adsorption of the dye was favourable using both adsorbents. The contact time to obtain equilibrium isotherms at 298-323 K was fixed at 4 hours for both adsorbents. For Reactive Blue 4 dye, Liu isotherm model gave the best fit for the equilibrium data. The maximum sorption capacity for adsorption of the dye occurred at 323 K, attaining values of 502.5 and 567.7 mg g{sup -1} for MWCNT and SWCNT, respectively. (author)

  6. Recent developments at the atomic and molecular data unit of the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    The Atomic and Molecular (A+M) Data Unit of the IAEA main purpose is to establish and maintain databases in support of nuclear fusion energy research. This encompasses a very large number of processes in atomic, molecular, and plasma - material interaction physics. Recent improvements and additions to these databases are presented. A prototype search engine, which searches five different sites for radiative data and two sites for electron impact excitation and ionization data is introduced. It is available at the IAEA, Weizmann Institute and GAPHYOR web sites. Data on erosion materials produced by the Co-ordinated research project (CRP) 'Plasma-interaction induced erosion of fusion reactor materials' was evaluated, fitted to physically realistic forms for angle and energy dependence and the resulting fits were added to the online electronic database. In a CRP on radiative power losses in plasmas, many lenghtly modelling calculations were carried out. In addition to providing the calculated radiated power, effective ionisation and recombination rate coefficients were derived. These data were stored along with the populations of the ion stages as well as the total radiation from each ion stage. Thus, it is possible to use these data to interpolate in temperature and electron density to obtain the radiated power at an arbitrary temperature and density. A preliminary version of a new interface to the bibliographic database at the A+M Data unit was developed, it allows the user to search by author and/or keyword. The resulting references are displayed along with a link to the home page of the journal where possible. A code for calculation electron impact excitation cross sections using the so-called 'average approximation' and a version of the Hartree-Fock atomic structure code were installed in the unit and can be run through an interface at the web page. (nevyjel)

  7. Photoelectrochemical production of atomic hydrogen at tungsten bronze/aqueous solution interface

    Energy Technology Data Exchange (ETDEWEB)

    Nagy, G.; Schiller, R.

    1988-12-01

    The cathodic photoeffect on hydrogenated sodium tungsten bronzes was studied in acid solutions under potentiostatic conditions. Solute effect proved the accompanying chemical reactions in the liquid phase to be brought about by hydrogen atoms. Kinetic analysis of the photocurrent showed that photoproduction and second-order recombination of the charge carriers in the solid are followed by reversible reduction of H/sup +/ at the interface. Finally H-atoms react with solutes like O/sub 2/, NO/sub 3//sup -/, Fe/sup 3+/, Fe(CN)/sub 6//sup 3-/, or tetranitromethane. The kinetics of charge carrier formation and of chemical reactions seem to be only weakly coupled, and the entire process can be described in terms of homogeneous kinetics showing diffusion and migration to be kinetically unimportant.

  8. Kinetics of carbonate dissolution in CO2-saturated aqueous system at reservoir conditions

    Science.gov (United States)

    Peng, Cheng; Crawshaw, John P.; Maitland, Geoffrey; Trusler, J. P. Martin

    2014-05-01

    In recent years, carbon capture and storage (CCS) has emerged as a key technology for limiting anthropogenic CO2 emissions while allowing the continued utilisation of fossil fuels. The most promising geological storage sites are deep saline aquifers because the capacity, integrity and injection economics are most favourable, and the environmental impact can be minimal. Many rock-fluid chemical reactions are known to occur both during and after CO2 injection in saline aquifers. The importance of rock-fluid reactions in the (CO2 + H2O) system can be understood in terms of their impact on the integrity and stability of both the formation rocks and cap rocks. The chemical interactions between CO2-acidified brines and the reservoir minerals can influence the porosity and permeability of the formations, resulting in changes in the transport processes occurring during CO2 storage. Since carbonate minerals are abundant in sedimentary rocks, one of the requirements to safely implement CO2 storage in saline aquifers is to characterise the reactivity of carbonate minerals in aqueous solutions at reservoir conditions. In this work, we reported measurements of the intrinsic rate of carbonate dissolution in CO2-saturated water under high-temperature high-pressure reservoir conditions extending up to 373 K and 14 MPa. The rate of carbonate dissolution in CO2-free HCl(aq) was also measured at ambient pressure at temperatures up to 353 K. Various pure minerals and reservoir rocks were investigated in this study, including single-crystals of calcite and magnesite, and samples of dolomite, chalks and sandstones. A specially-designed batch reactor system, implementing the rotating disc technique, was used to obtain the intrinsic reaction rate at the solid/liquid interface, free of mass transfer effects. The effective area and mineralogy of the exposed surface was determined by a combination of surface characterisation techniques including XRD, SEM, EDX and optical microscopy. The

  9. Application of adsorption process by activated carbon derived from scrap tires for Pb+2 removal from aqueous solutions

    OpenAIRE

    Edris Hoseinzadeh; Ali Reza Rahmani; Ghorban Asgari; Mohamad Taghi Samadi; Ghodratollah Roshanaei; Mohammad Reza Zare

    2013-01-01

    Background and Aim: Heavy metals have been recognized as very poisonous elements and their discharge into water sources can cause damaging effects on human and environmental health. The present study aimed at producing activated carbon from scrap tires and using it in removing Pb+2 from synthetic aqueous solutions. Materials and Methods: In this experimental study, activated carbon powder was derived from scrap tires under laboratory conditions. The effect of Pb (II) ions wi...

  10. Preparation and Utilization of Kapok Hull Carbon for the Removal of Rhodamine-B from Aqueous Solution

    OpenAIRE

    P. S. Syed Shabudeen; R. Venckatesh; S. Pattabhi

    2006-01-01

    A carbonaceous sorbent prepared from the indegeneous agricultural waste (which is facing solid waste disposal problem) Kapok Hull, by acid treatment was tested for its efficiency in removing basic dyes. Batch kinetic and isotherm experiments were conducted to determine the sorption and desorption of the Rhodamine-B from aqueous solution with activated carbon. The factors affecting the rate processes involved in the removal of dye for initial dye concentration, agitation time, and carbon dose ...

  11. The efficiency of magnetic carbon activated by iron oxide nanoparticles in removing of Cu (II) from aqueous solutions

    OpenAIRE

    Salehe Salehnia; Behnam Barikbin; Hadighe Dorri

    2016-01-01

    Background and Aim: Copper ions, due to forming complexes with organic and mineral compounds, can have worrying effects on health and environment. In the present study, the effect of powdered magnetic carbon activated by iron-oxide nanoparticles in removing of CU (V; II) from aqueous solutions was assessed. Materials and Methods: This experimental study aimed at determining the effect of powdered magnetic carbon activated  by iron-oxide nanoparticles  parameters including PH, co...

  12. Highlights of the Third United Nations International Conference on the Peaceful Uses of Atomic Energy

    International Nuclear Information System (INIS)

    The Third International Conference on the Peaceful Uses of Atomic Energy did not produce any spectacular data. Many technical details of recent work were reported and the results of work already published were confirmed and amplified. It became quite clear at the Conference that atomic energy has now reached the industrial stage in various countries. The Conference can thus be seen as a sort of landmark marking the beginning of the era of nuclear power

  13. International bulletin on atomic and molecular data for fusion. No. 11

    International Nuclear Information System (INIS)

    This bulletin deals with atomic and molecular data for fusion. A bibliography for the most recent data presented in the document is provided. Work in progress is briefly reported. The bulletin contains a list of references the publications on controlled fusion and plasma physics for 1979. It contains an index to the contributed papers presented at the 11th International Conference on the Physics of Electronics and Atomic Collision (ICPEAC) held in Kyoto (Japan) in summer 1979

  14. Visualization of arrangements of carbon atoms in graphene layers by Raman mapping and atomic-resolution TEM

    KAUST Repository

    Cong, Chunxiao

    2013-02-01

    In-plane and out-of-plane arrangements of carbon atoms in graphene layers play critical roles in the fundamental physics and practical applications of these novel two-dimensional materials. Here, we report initial results on the edge/crystal orientations and stacking orders of bi-and tri-layer graphene (BLG and TLG) from Raman spectroscopy and transmission electron microscopy (TEM) experiments performed on the same sample. We introduce a new method of transferring graphene flakes onto a normal TEM grid. Using this novel method, we probed the BLG and TLG flakes that had been previously investigated by Raman scattering with high-resolution (atomic) TEM.

  15. New dimensions in nonproliferation -- An International Atomic Energy Agency view

    International Nuclear Information System (INIS)

    Four years ago, Saddam Hussein invaded Kuwait with the intention of annexing it as Iraq's 19th state. The disclosure of the Iraqi nuclear weapons program in the aftermath of the Gulf War--through the IAEA inspections--signaled the end of one proliferation era and the start of the next. In the author's remarks here, he has found it useful to identify four distinct proliferation eras, each with different features, each calling for different emphasis in international nonproliferation efforts. They provide a convenient way to look at the history of nonproliferation, and to look into the future and to the new dimensions in nonproliferation that are slowly emerging. Since the Gulf War, the nuclear world experienced a series of events of fundamental significance that changed the nature of nonproliferation, forcing changes in the mission of the IAEA and its methods. Certainly some of these events came in the form of unpleasant surprises, such as in Iraq, but very positive progress was also made on other fronts. He would like to share some perceptions of the events creating the present situation, and some views anticipating the requirements most likely to emerge in the coming years

  16. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas

    Energy Technology Data Exchange (ETDEWEB)

    Brent Constantz; Randy Seeker; Martin Devenney

    2010-06-30

    Calera's innovative Mineralization via Aqueous Precipitation (MAP) technology for the capture and conversion of CO{sub 2} to useful materials for use in the built environment was further developed and proven in the Phase 1 Department of Energy Grant. The process was scaled to 300 gallon batch reactors and subsequently to Pilot Plant scale for the continuous production of product with the production of reactive calcium carbonate material that was evaluated as a supplementary cementitious material (SCM). The Calera SCM{trademark} was evaluated as a 20% replacement for ordinary portland cement and demonstrated to meet the industry specification ASTM 1157 which is a standard performance specification for hydraulic cement. The performance of the 20% replacement material was comparable to the 100% ordinary portland cement control in terms of compressive strength and workability as measured by a variety of ASTM standard tests. In addition to the performance metrics, detailed characterization of the Calera SCM was performed using advanced analytical techniques to better understand the material interaction with the phases of ordinary portland cement. X-ray synchrotron diffraction studies at the Advanced Photon Source in Argonne National Lab confirmed the presence of an amorphous phase(s) in addition to the crystalline calcium carbonate phases in the reactive carbonate material. The presence of carboaluminate phases as a result of the interaction of the reactive carbonate materials with ordinary portland cement was also confirmed. A Life Cycle Assessment was completed for several cases based on different Calera process configurations and compared against the life cycle of ordinary portland cement. In addition to the materials development efforts, the Calera technology for the production of product using an innovative building materials demonstration plant was developed beyond conceptual engineering to a detailed design with a construction schedule and cost estimate.

  17. International bulletin on atomic and molecular data for fusion. No. 52

    International Nuclear Information System (INIS)

    This bulletin is published by the International Atomic Energy Agency to provide atomic and molecular data relevant to fusion research and technology. In part 1 the indexed papers are listed separately for (i) structure and spectra (energy levels, wavelengths, transition probabilities, oscillator strengths, interatomic potentials); (ii) atomic and molecular collisions (photon collisions, electron collisions, heavy-particle collisions); and (iii) surface interactions (sputtering, chemical reactions, trapping and detrapping, adsorption, desorption, reflection, and secondary electron emission). Part 2 contains the bibliographic data, essentially for the above listed topics

  18. The International Colloquium on Atomic Spectra and Oscillator Strengths for Astrophysical and Laboratory Plasmas

    Science.gov (United States)

    Sugar, J.; Leckrone, D.

    1993-01-01

    This was the fourth in a series of colloquia begun at the University of Lund, Sweden in 1983 and subsequently held in Toledo, Ohio and Amsterdam, The Netherlands. The purpose of these meetings is to provide an international forum for communication between major users of atomic spectroscopic data and the providers of these data. These data include atomic wavelengths, line shapes, energy levels, lifetimes, and oscillator strengths. Speakers were selected from a wide variety of disciplines including astrophysics, laboratory plasma research, spectrochemistry, and theoretical and experimental atomic physics.

  19. International bulletin on atomic and molecular data for fusion. Nos. 50-51

    International Nuclear Information System (INIS)

    This bulletin is published by the International Atomic Energy Agency to provide atomic and molecular data relevant to fusion research and technology. In part 1 the indexed papers are listed separately for (i) structure and spectra (energy levels, wavelengths, transition probabilities, oscillator strengths, polarizabilities, electric moments, interatomic potentials); (ii) atomic and molecular collisions (photon collisions, electron collisions, heavy-particle collisions); and (iii) surface interactions (sputtering, chemical reactions, trapping and detrapping, adsorption, desorption, reflection, and secondary electron emission). Part 2 contains the bibliographic data, essentially for the above listed topics

  20. Determination of semi-empirical correlation between hydrogen and manganese atomic ratio and manganese sulphate concentration in aqueous solution

    International Nuclear Information System (INIS)

    The Manganese Bath (MB) is a widely used technique for measuring the emission rate of the neutrons source. In a measurement the source is placed in the center of an aqueous solution of manganese sulfate (MnSO4), large enough to ensure that only a very small fraction of neutrons emitted by the source escape of the system. Why not be the only single core manganese to absorb the neutrons from the source and any other losses, the MB uses several parameters arranged in the form of four key terms that make algebraic form of the final value neutron emission from a source: saturation activity A(t), the sensitivity (ε) of Standardization System, the fraction of thermal neutrons (F) caught by 55Mn which in particular the ratio between hydrogen atoms and manganese, and the correction parameter K related to the escape of neutrons from the solution, the capture of neutrons by the source material and the capture of fast neutrons in the solution is determined by mathematical simulation of MB. The purpose of this study is to establish a functional relationship, using the gravimetric method, between the physical density, concentration and atoms ratio of hydrogen and manganese in the solution of the MB and with forecasts that do stop these values so that different concentrations for MB may be held, with the objective to reduce uncertainties in the parameters of the correction of K and F, therefore reducing the uncertainty in the emission rate source. (author)

  1. The international atom: evolution of radiation control programs.

    Science.gov (United States)

    Bradley, F J

    2002-07-01

    Under the Atoms for Peace program, Turkey received a one MWt swimming pool reactor in 1962 that initiated a health physics program for the reactor and a Radiation Control Program (RCP) for the country's use of ionizing radiation. Today, over 13,000 radiation workers, concentrated in the medical field, provide improved medical care with 6,200 x-ray units, including 494 CAT scanners, 222 radioimmunoassay (RIA) labs and 42 radiotherapy centers. Industry has a large stake in the safe use of ionizing radiation with over 1,200 x-ray and gamma radiography and fluoroscopic units, 2,500 gauges in automated process control and five irradiators. A 48-person RCP staff oversees this expanded radiation use. One incident involving a spent 3.3 TBq (88 Ci) 60Co source resulted in 10 overexposures but no fatalities. Taiwan received a 1.6 MWt swimming pool reactor in 1961 and rapidly applied nuclear technology to the medical and industrial fields. Today, there are approximately 24,000 licensed radiation workers in nuclear power field, industry, medicine and academia. Four BWRs and two PWRs supply about 25% of the island's electrical power needs. One traumatic event galvanized the RCP when an undetermined amount of 60Co was accidentally incorporated into reinforcing bars, which in turn were incorporated into residential and commercial buildings. Public exposures were estimated to range up to 15 mSv (1.3 rem) per annum. There were no reported ill effects, except possibly psychological, to date. The RCP now has instituted stringent control measures to ensure radiation-free dwellings and work places. Albania's RCP is described as it evolved since 1972. Regulations were promulgated which followed the IAEA Basic Safety Standards of that era. With 525 licenses and 600 radiation workers, the problem was not in the regulations per se but in their enforcement. The IAEA helped to upgrade the RCP as the economy evolved from one that was centrally planned economy to a free market economy. As this

  2. Hydrogen internal friction and interaction of solute atoms in niobium- and vanadium-based alloys

    International Nuclear Information System (INIS)

    A computer model has been proposed to be used to calculate the internal friction spectrum, caused by the ''diffusion under stress'' of hydrogen atoms in a solid solution with a b.c.c. lattice containing substitutional atoms. The model takes into account the long-range pair interaction of dissolved atoms. It is suggested that such interaction acts on diffusion by producing short-range order of mobile hydrogen atoms and by changing their energy. These changes occur in the tetrahedral (before the jump) as well as in the octahedral (at the saddle point of the diffusion barrier) interstitial sites and, therefore, produce local changes of the hydrogen diffusion activation energy (the activation energy of internal friction). The relaxation strength is calculated from the local fields of atomic displacements around every atom that participates in diffusion. The model has been used to study the nature of hydrogen relaxation in Ti- and Zr-containing Nb- and V-based alloys and to calculate the ''chemical'' interaction energy of the H(D)-Ti(Zr) pairs. It was shown that the hydrogen relaxation mechanism in Nb(V)-Ti(Zr)-H(D) alloys consists in diffusion under stress of hydrogen or deuterium atoms in the vicinity of single substitutional atoms at low concentration of substitutional atoms and high hydrogen or deuterium concentration, and in the vicinity of substitutional pairs - at high concentration of substitutional atoms and low hydrogen or deuterium concentration. The ''chemical'' interaction H(D)-Ti(Zr) in niobium and vanadium is stronger or is of the same order, as the strain-induced (elastic) interaction. (orig.)

  3. Atomic force microscopy based nanoindentation study of onion abaxial epidermis walls in aqueous environment

    Science.gov (United States)

    Xi, Xiaoning; Kim, Seong H.; Tittmann, Bernhard

    2015-01-01

    An atomic force microscopy based nanoindentation method was employed to study how the structure of cellulose microfibril packing and matrix polymers affect elastic modulus of fully hydrated primary plant cell walls. The isolated, single-layered abaxial epidermis cell wall of an onion bulb was used as a test system since the cellulose microfibril packing in this cell wall is known to vary systematically from inside to outside scales and the most abundant matrix polymer, pectin, can easily be altered through simple chemical treatments such as ethylenediaminetetraacetic acid and calcium ions. Experimental results showed that the pectin network variation has significant impacts on the cell wall modulus, and not the cellulose microfibril packing.

  4. Atomic force microscopy based nanoindentation study of onion abaxial epidermis walls in aqueous environment

    International Nuclear Information System (INIS)

    An atomic force microscopy based nanoindentation method was employed to study how the structure of cellulose microfibril packing and matrix polymers affect elastic modulus of fully hydrated primary plant cell walls. The isolated, single-layered abaxial epidermis cell wall of an onion bulb was used as a test system since the cellulose microfibril packing in this cell wall is known to vary systematically from inside to outside scales and the most abundant matrix polymer, pectin, can easily be altered through simple chemical treatments such as ethylenediaminetetraacetic acid and calcium ions. Experimental results showed that the pectin network variation has significant impacts on the cell wall modulus, and not the cellulose microfibril packing

  5. Atomic force microscopy based nanoindentation study of onion abaxial epidermis walls in aqueous environment

    Energy Technology Data Exchange (ETDEWEB)

    Xi, Xiaoning; Tittmann, Bernhard [Department of Engineering Science and Mechanics, Pennsylvania State University, University Park, Pennsylvania 16802 (United States); Kim, Seong H. [Department of Chemical Engineering, Pennsylvania State University, University Park, Pennsylvania 16802 (United States)

    2015-01-14

    An atomic force microscopy based nanoindentation method was employed to study how the structure of cellulose microfibril packing and matrix polymers affect elastic modulus of fully hydrated primary plant cell walls. The isolated, single-layered abaxial epidermis cell wall of an onion bulb was used as a test system since the cellulose microfibril packing in this cell wall is known to vary systematically from inside to outside scales and the most abundant matrix polymer, pectin, can easily be altered through simple chemical treatments such as ethylenediaminetetraacetic acid and calcium ions. Experimental results showed that the pectin network variation has significant impacts on the cell wall modulus, and not the cellulose microfibril packing.

  6. Atomic scale mass delivery driven by bend kink in single walled carbon nanotube

    International Nuclear Information System (INIS)

    The possibility of atomic scale mass delivery by bend kink in single walled carbon nanotube was investigated with the aid of molecular dynamics simulation. By keeping the bending angle while moving the tube end, the encapsulated atomic scale mass such as atom, molecule and atom group were successfully delivered through the nanotube. The van der Waals interaction between the encapsulated mass and the tube wall provided the driving force for the delivery. There were no dramatic changes in the van der Waals interaction, and a smooth and steady delivery was achieved when constant loading rate was applied. The influence of temperature on the atom group delivery was also analyzed. It is found raising temperature is harmful to the smooth movement of the atom group. However, the delivery rate can be promoted under higher temperature when the atom group is situated before the kink during the delivery.

  7. USEPA METHOD STUDY 38 - SW-846 METHOD 3010, ACID DIGESTION OF AQUEOUS SAMPLES AND EXTRACTS FOR TRACE METALS BY FLAME ATOMIC ABSORPTION SPECTROSCOPY

    Science.gov (United States)

    An interlaboratory collaborative study was conducted on SW-846 Method 3010, "Acid Digestion of Aqueous Samples and Extracts for Total Metals for Analysis by Flame Atomic Absorption Spectroscopy", to determine the mean recovery and precision for analyses of 21 trace metals in surf...

  8. Measurement of 5-eV atomic oxygen using carbon-based films: preliminary results

    OpenAIRE

    White, C de B; Roberts, G. T.; Chambers, A.R.

    2005-01-01

    Carbon-based sensors have been developed to measure the atmospheric neutral atomic oxygen (AO) flux experienced by spacecraft in low Earth orbit. Thin- and thick-film carbon sensor elements were deposited onto an alumina substrate between thick-film gold tracks and silver palladium solder pads. AO flux is deduced by measuring resistance changes as the carbon film erodes and applying a simple theory. A wide range of responses were observed that are dependent on the deposition process and post ...

  9. Atomic scale observations of bainite transformation in a high carbon high silicon steel

    OpenAIRE

    García Caballero, Francisca; Miller, M. K.; Babu, S. S.; García Mateo, Carlos

    2007-01-01

    A fine-scale bainitic microstructure with high strength and high toughness has been achieved by transforming austenite at 200 ºC. X-ray diffraction analysis showed the carbon concentration of these bainitic ferrite plates to be higher than expected from paraequilibrium. Atom probe tomography revealed that a substantial quantity of carbon was trapped at dislocations in the vicinity of the ferrite/austenite interface. These results suggest that the carbon trapping at dislocations...

  10. Early Stages of the Chemical Vapor Deposition of Pyrolytic Carbon Investigated by Atomic Force Microscopy

    OpenAIRE

    Pfrang, Andreas; WAN Yong-Zhong; Schimmel, Thomas

    2009-01-01

    The early stages of chemical vapor deposition of pyrolytic carbon on planar silicon substrates were studied by the atomic force microscopy-based technique of chemical contrast imaging. Short deposition times were chosen to focus on the early stages of the deposition process, and three different types of nucleation were found: random nucleation of single islands, nucleation of carbon islands along lines and secondary nucleation which corresponds to the nucleation of carbon islands at the edges...

  11. Bright carbonate deposits as evidence of aqueous alteration on (1) Ceres

    Science.gov (United States)

    de Sanctis, M. C.; Raponi, A.; Ammannito, E.; Ciarniello, M.; Toplis, M. J.; McSween, H. Y.; Castillo-Rogez, J. C.; Ehlmann, B. L.; Carrozzo, F. G.; Marchi, S.; Tosi, F.; Zambon, F.; Capaccioni, F.; Capria, M. T.; Fonte, S.; Formisano, M.; Frigeri, A.; Giardino, M.; Longobardo, A.; Magni, G.; Palomba, E.; McFadden, L. A.; Pieters, C. M.; Jaumann, R.; Schenk, P.; Mugnuolo, R.; Raymond, C. A.; Russell, C. T.

    2016-08-01

    The typically dark surface of the dwarf planet Ceres is punctuated by areas of much higher albedo, most prominently in the Occator crater. These small bright areas have been tentatively interpreted as containing a large amount of hydrated magnesium sulfate, in contrast to the average surface, which is a mixture of low-albedo materials and magnesium phyllosilicates, ammoniated phyllosilicates and carbonates. Here we report high spatial and spectral resolution near-infrared observations of the bright areas in the Occator crater on Ceres. Spectra of these bright areas are consistent with a large amount of sodium carbonate, constituting the most concentrated known extraterrestrial occurrence of carbonate on kilometre-wide scales in the Solar System. The carbonates are mixed with a dark component and small amounts of phyllosilicates, as well as ammonium carbonate or ammonium chloride. Some of these compounds have also been detected in the plume of Saturn’s sixth-largest moon Enceladus. The compounds are endogenous and we propose that they are the solid residue of crystallization of brines and entrained altered solids that reached the surface from below. The heat source may have been transient (triggered by impact heating). Alternatively, internal temperatures may be above the eutectic temperature of subsurface brines, in which case fluids may exist at depth on Ceres today.

  12. Removals of aqueous sulfur dioxide and hydrogen sulfide using CeO2-NiAl-LDHs coating activated carbon and its mix with carbon nano-tubes

    KAUST Repository

    Li, Jing

    2015-07-01

    Ce-doped NiAl/layered double hydroxide was coated at activated carbon by urea hydrolysis method (CeO2-NiAl-LDHs/AC) in one pot, which was characterized by X-ray diffraction, infrared spectra, field emission scanning electron microscope and electrochemical techniques. CeO2-NiAl-LDHs/AC shows good uptake for aqueous sulfur dioxide (483.09mg/g) and hydrogen sulfide (181.15mg/g), respectively at 25°C. Meanwhile, the electrochemical removals of aqueous sulfur dioxide and hydrogen sulfide were respectively investigated at the mix of CeO2-NiAl-LDHs/AC and carbon nano-tubes modified homed paraffin-impregnated electrode. Both sulfur dioxide and hydrogen sulfide could be effectively oxidized to sulfuric acid at 1.0V in alkaline aqueous solution. © 2015 Elsevier B.V.

  13. Panorama 2014 - Overview of new carbon markets at international level

    International Nuclear Information System (INIS)

    Although carbon prices on the European Emissions Trading Scheme (ETS) are at their lowest since 2008 and international negotiations in relation to the United Nations Framework Convention on Climate Change have been stagnating since the 2009 Copenhagen Agreement, nearly seventeen emissions trading markets have been identified at international level. Without counting the European ETS which has existed since 2005, eleven new markets have emerged since 2008 and a further five are set to commence trading in 2014. Of these eleven active markets, five are in Asia, three are in North America, one is in Oceania, one is in Central Asia and one is in Europe. It should be pointed out that to date, no markets are scheduled to begin trading in Africa. Although four markets have announced their intention to work together between now and 2020, the creation of an international emissions trading scheme is not on the immediate horizon. (author)

  14. International Co-Operation on the Safety of Nuclear Power Plants within the Framework of the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    The Director General has received from three Member States the following communications regarding international co-operation on the safety of nuclear power plants within the framework of the International Atomic Energy Agency: (i) Letter dated 17 May 1979 from the Federal Minister for Research and Development of the Federal Republic of Germany, together with the explanation of the proposal made by the Government of the Federal Republic of Germany; (ii) Letter dated 21 May 1979 from the Resident Representative of Brazil to the Agency; (iii) Letter dated 31 May 1979 from the Minister for Foreign Affairs of Sweden.

  15. Study on nitrogen doped carbon atom chains with negative differential resistance effect

    Science.gov (United States)

    Shen, Ji-Mei; Liu, Jing; Min, Yi; Zhou, Li-Ping

    2016-05-01

    Recent calculations (Mahmoud and Lugli, 2013, [21]) of gold leads sandwiching carbon chains which are separated by diphenyl-dimethyl demonstrated that the negative differential resistance (NDR) effect appears only for "odd" numbers of carbon atoms. In this paper, according to a first-principles study based on non-equilibrium Green's function combining density functional theory, we find that the NDR effect appears both for "odd" and for "even" numbers of carbon atoms when the chains are doped by nitrogen atom. Our calculations remove the restriction of "odd/even" chains for the NDR effect, which may promise the potential applications of carbon chains in the nano-scale or molecular devices in the future.

  16. Atomic-scale study of the role of carbon on boron clustering

    International Nuclear Information System (INIS)

    Boron (BF2, 20 keV, 3.14/cm2) and carbon (13 keV, 1015/cm2) implanted silicon annealed at 800 oC during 30 min or at 1000 oC during 10 s has been investigated using a laser-assisted wide-angle tomographic atom probe (LaWaTAP) instrument. Boron-silicon clusters containing ∼ 1.3 at.% of boron atoms have been observed in boron implanted silicon with a concentration exceeding the solubility limit. Often identified as BICs, they are interpreted as a metastable phase. Furthermore, addition of carbon clearly reduced the clustering of boron. This was interpreted as a diminution of boron diffusion or as an increase of the solubility limit of boron. Carbon-silicon clusters containing ∼ 1.5 at.% of carbon atoms were observed, maybe the precursors of the SiC phase.

  17. Sorption study of uranium on carbon spheres hydrothermal synthesized with glucose from aqueous solution

    International Nuclear Information System (INIS)

    The ability of oxygen-rich carbon spheres (CSs) produced by hydrothermal carbonization with the glucose has been explored for the removal and recovery of uranium from aqueous solutions. The micro-morphology and structure of CSs were characterized by FT-IR and SEM. The influences of different experimental parameters such as solution pH, initial concentration, contact time, ionic strength and temperature on adsorption were investigated. The CSs showed the highest uranium sorption capacity at initial pH of 6.0 and contact time of 25 min. Adsorption kinetics was better described by the pseudo-second-order model and adsorption process could be well defined by the Langmuir isotherm. The thermodynamic parameters, ΔGdeg(298 K), ΔHdeg and ΔSdeg were determined to be -16.88, 12.09 kJ mol-1 and 197.87 J mol-1 K-1, respectively, which demonstrated the sorption process of CSs towards U(VI) was feasible, spontaneous and endothermic in nature. The adsorbed CSs could be effectively regenerated by 0.05 mol/L HCl solution for the removal and recovery of U(VI). Complete removal (99.9 %) of U(VI) from 1.0 L industry wastewater containing 15.0 mg U(VI) ions was possible with 3.0 g CSs. (author)

  18. Sodium phthalamates as corrosion inhibitors for carbon steel in aqueous hydrochloric acid solution

    International Nuclear Information System (INIS)

    Highlights: → N-Alkyl-sodium phthalamates as corrosion inhibitors for industry in acidic medium. → Compounds behaved as mixed type inhibitors and followed Langmuir adsorption isotherm. → Efficiencies were proportional to aliphatic chain length and inhibitor concentration. → Iron complexes and chelates with phthalamates contributed to carbon steel protection. - Abstract: Three compounds of N-alkyl-sodium phthalamates were synthesized and tested as corrosion inhibitors for carbon steel in 0.5 M aqueous hydrochloric acid. Tests showed that inhibitor efficiencies were related to aliphatic chain length and dependent on concentration. N-1-n-tetradecyl-sodium phthalamate displayed moderate efficiency against uniform corrosion, 42-86% at 25 deg. C and 25-60% at 40 oC. Tests indicated that compounds behave as mixed type inhibitors where molecular adsorption on steel followed Langmuir isotherm, whereas thermodynamic suggested that a physisorption process occurred. XPS analysis confirmed film formation on surface, where Fe+2 complexes and Fe+2 chelates with phthalamates prevented steel from further corrosion.

  19. Ciprofloxacin adsorption from aqueous solution onto chemically prepared carbon from date palm leaflets

    Institute of Scientific and Technical Information of China (English)

    El-Said Ibrahim El-Shafey; Haider Al-Lawati; Asmaa Soliman Al-Sumri

    2012-01-01

    A chemically prepared carbon was synthesized from date palm leaflets via sulphuric acid carbonization at 160℃.Adsorption of ciprofloxacin (CIP) from aqueous solution was investigated in terms of time,pH,concentration,temperature and adsorbent status (wet and dry).The equilibrium time was found to be 48 hr.The adsorption rate was enhanced by raising the temperature for both adsorbents,with adsorption data fitting a pseudo second-order model well.The activation energy,Ea,was found to be 17 kJ/mol,indicating a diffusion-controlled,physical adsorption process.The maximum adsorption was found at initial pH 6.The wet adsorbent showed faster removal with higher uptake than the dry adsorbent,with increased performance as temperature increased (25-45℃ ).The equilibrium data were found to fit the Langmuir model better than the Freundlich model.The thermodynamic parameters showed that the adsorption process is spontaneous and endothermic.The adsorption mechanism is mainly related to cation exchange and hydrogen bonding.

  20. The Use of Microwave Derived Activated Carbon for Removal of Heavy Metal in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Rafeah Wahi

    2011-09-01

    Full Text Available Palm oil processing waste which is palm oil kernel shell (POKS was converted to activated carbon (POKS AC through 7 min microwave pyrolysis at temperature 270 °C followed by chemical activation using NaOH and HCl. The adsorption study on Ni(II, Cu(II and Cr(IV was conducted to evaluate the efficiency of the prepared activated carbon to remove heavy metal. The adsorption capacity was determined as a function of adsorbate initial concentration and adsorbent dosage. Based on Langmuir isotherm, Ni(II showed highest adsorption capacity of 40.98 mg/g, followed by Cr(IV and Cu(II with adsorption capacity of 40.60 mg/g and 13.69 mg/g, respectively. Cr(IV and Cu(II showed better fitting to Freundlich isotherm model with high correlation regression indicating the applicability of heterogeneous adsorption. Ni(II show better fitting with Langmuir isotherm that indicate monolayer coverage. The use of POKS AC is not only effective for adsorption of Cr(IV, Ni(II and Cu(II in aqueous solution but also helps to overcome the over abundance of POKS waste problem.

  1. Effect of aqueous electrolytes on the electrochemical behaviors of supercapacitors based on hierarchically porous carbons

    Science.gov (United States)

    Zhang, Xiaoyan; Wang, Xianyou; Jiang, Lanlan; Wu, Hao; Wu, Chun; Su, Jingcang

    2012-10-01

    Hierarchically porous carbons (HPCs) have been prepared by sol-gel self-assembly technology with nickel oxide and surfactant as the dual template. The porous carbons are further activated by nitric acid. The electrochemical behaviors of supercapacitors using HPCs as electrode material in different aqueous electrolytes, e.g., (NH4)2SO4, Na2SO4, H2SO4 and KOH are studied by cyclic voltametry, galvanostatic charge/discharge, cyclic life, leakage current, self-discharge and electrochemical impedance spectroscopy. The results demonstrate that the supercapacitors in various electrolytes perform definitely capacitive behaviors; especially in 6 M KOH electrolyte the supercapacitor represents the best electrochemical performance, the shortest relaxation time, and nearly ideal polarisability. The energy density of 8.42 Wh kg-1 and power density of 17.22 kW kg-1 are obtained at the operated voltage window of 1.0 V. Especially, the energy density of 11.54 Wh kg-1 and power density of 10.58 kW kg-1 can be achieved when the voltage is up to 1.2 V.

  2. Degradation of triclosan in aqueous solution by dielectric barrier discharge plasma combined with activated carbon fibers.

    Science.gov (United States)

    Xin, Lu; Sun, Yabing; Feng, Jingwei; Wang, Jian; He, Dong

    2016-02-01

    The degradation of triclosan (TCS) in aqueous solution by dielectric barrier discharge (DBD) plasma with activated carbon fibers (ACFs) was investigated. In this study, ACFs and DBD plasma coexisted in a planar DBD plasma reactor, which could synchronously achieve degradation of TCS, modification and in situ regeneration of ACFs, enhancing the effect of recycling of ACFs. The properties of ACFs before and after modification by DBD plasma were characterized by BET and XPS. Various processing parameters affecting the synergetic degradation of TCS were also investigated. The results exhibited excellent synergetic effects in DBD plasma-ACFs system on TCS degradation. The degradation efficiency of 120 mL TCS with initial concentration of 10 mg L(-1) could reach 93% with 1 mm thick ACFs in 18 min at input power of 80 W, compared with 85% by single DBD plasma. Meanwhile, the removal rate of total organic carbon increased from 12% at pH 6.26-24% at pH 3.50. ACFs could ameliorate the degradation efficiency for planar DBD plasma when treating TCS solution at high flow rates or at low initial concentrations. A possible degradation pathway of TCS was investigated according to the detected intermediates, which were identified by liquid chromatography-hybrid quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) combined with theoretical calculation of Gaussian 09 program. PMID:26421625

  3. ADSORPTION OF Cr(VI FROM AQUEOUS SOLUTION USING CARBON-MICROSILICA COMPOSITE ADSORBENT

    Directory of Open Access Journals (Sweden)

    DEYI ZHANG

    2012-03-01

    Full Text Available In this work, Microsilica, one kind of industry solid waste material, was utilized firstly to prepare a carbon-Microsilica composite adsorbent from a partial carbonization, mixture and sulfoxidation process and was proposed for the removal of Cr(VI from solutions. The surface chemistry characteristics of the prepared adsorbent were analysis by XPS and FT-IR. The characterization results indicated that an abundant of oxygen functional groups, such as hydroxyl, carboxyl and sulfonic groups, were introduced into the surface of the prepared composite adsorbent. Meanwhile, the adsorption characteristics of Cr(VI onto the adsorbent in aqueous solutions was studied as a function of solution pH, ionic strength, contact time, and temperature. The results showed that Cr(VI adsorption onto the adsorbent is strongly dependent on pH and, to a lesser extent, ionic strength. Kinetics data were found to follow the pseudo-second-order kinetic model while the adsorption data corresponded to L-shape adsorption isotherm which corresponds to the classification of Giles. Activation thermodynamic parameters, such as activation enthalpy (ΔH*, activation entropy (ΔS*, activation Gibbs free energy (ΔG* and activation energy (E, have been evaluated and the possible adsorption mechanism also was suggested.

  4. Direct chemical conversion of graphene to boron- and nitrogen- and carbon-containing atomic layers

    Science.gov (United States)

    Gong, Yongji; Shi, Gang; Zhang, Zhuhua; Zhou, Wu; Jung, Jeil; Gao, Weilu; Ma, Lulu; Yang, Yang; Yang, Shubin; You, Ge; Vajtai, Robert; Xu, Qianfan; MacDonald, Allan H.; Yakobson, Boris I.; Lou, Jun; Liu, Zheng; Ajayan, Pulickel M.

    2014-01-01

    Graphene and hexagonal boron nitride are typical conductor and insulator, respectively, while their hybrids hexagonal boron carbonitride are promising as a semiconductor. Here we demonstrate a direct chemical conversion reaction, which systematically converts the hexagonal carbon lattice of graphene to boron nitride, making it possible to produce uniform boron nitride and boron carbonitride structures without disrupting the structural integrity of the original graphene templates. We synthesize high-quality atomic layer films with boron-, nitrogen- and carbon-containing atomic layers with full range of compositions. Using this approach, the electrical resistance, carrier mobilities and bandgaps of these atomic layers can be tuned from conductor to semiconductor to insulator. Combining this technique with lithography, local conversion could be realized at the nanometre scale, enabling the fabrication of in-plane atomic layer structures consisting of graphene, boron nitride and boron carbonitride. This is a step towards scalable synthesis of atomically thin two-dimensional integrated circuits.

  5. A nine-atom rhodium–aluminum oxide cluster oxidizes five carbon monoxide molecules

    Science.gov (United States)

    Li, Xiao-Na; Zhang, Hua-Min; Yuan, Zhen; He, Sheng-Gui

    2016-01-01

    Noble metals can promote the direct participation of lattice oxygen of very stable oxide materials such as aluminum oxide, to oxidize reactant molecules, while the fundamental mechanism of noble metal catalysis is elusive. Here we report that a single atom of rhodium, a powerful noble metal catalyst, can promote the transfer of five oxygen atoms to oxidize carbon monoxide from a nine-atom rhodium–aluminum oxide cluster. This is a sharp improvement in the field of cluster science where the transfer of at most two oxygen atoms from a doped cluster is more commonly observed. Rhodium functions not only as the preferred trapping site to anchor and oxidize carbon monoxide by the oxygen atoms in direct connection with rhodium but also the primarily oxidative centre to accumulate the large amounts of electrons and the polarity of rhodium is ultimately transformed from positive to negative. PMID:27094921

  6. A nine-atom rhodium-aluminum oxide cluster oxidizes five carbon monoxide molecules.

    Science.gov (United States)

    Li, Xiao-Na; Zhang, Hua-Min; Yuan, Zhen; He, Sheng-Gui

    2016-01-01

    Noble metals can promote the direct participation of lattice oxygen of very stable oxide materials such as aluminum oxide, to oxidize reactant molecules, while the fundamental mechanism of noble metal catalysis is elusive. Here we report that a single atom of rhodium, a powerful noble metal catalyst, can promote the transfer of five oxygen atoms to oxidize carbon monoxide from a nine-atom rhodium-aluminum oxide cluster. This is a sharp improvement in the field of cluster science where the transfer of at most two oxygen atoms from a doped cluster is more commonly observed. Rhodium functions not only as the preferred trapping site to anchor and oxidize carbon monoxide by the oxygen atoms in direct connection with rhodium but also the primarily oxidative centre to accumulate the large amounts of electrons and the polarity of rhodium is ultimately transformed from positive to negative. PMID:27094921

  7. Study on the π-meson capture by carbon atoms in organic molecules

    International Nuclear Information System (INIS)

    It is established that the intensity of π--meson interception by carbon in organic molecules Csub(m)Hsub(n) differs in the hydrocarbon series from that in the gas mixtures H2+Csub(m)Hsub(n). It is suggested that this difference is due to the different excitation energies of the hydrogen mesic atoms produced on the free (H2) and on the chemically bound (Z-H) hydrogen. The grouping of the atoms Z into molecules, their surrounding by hydrogen atoms, and singularities in the chemical bonds of the Z atoms exert on noticeable influence on the interception

  8. Atomically resolved surface structures of vapor deposited amorphous silicon-carbon alloys: An atomic force microscopy and spectroscopic study

    International Nuclear Information System (INIS)

    Silicon carbide alloys are widely used in high-tech applications due to their interesting combination of chemical, mechanical and electronic properties. Growing thin films of this material in a simple and controlled way is a hot topic in modern material's science. In particular, the possibility to tailor the film properties just by tuning the deposition temperature would be an important progress. In the present work amorphous silicon-carbon alloys thin films have been deposited by electron beam sublimation of a poly-crystalline silicon carbide target in vacuum environment. The deposition temperature was varied from Room Temperature to about 1300 K. The resulting films were analyzed by means of Ultra High Vacuum-Atomic Force Microscopy (UHV-AFM) down to even atomic resolution. The observed features agree with literature data, e.g. interatomic bond lengths, as achieved by others methods, and the structural arrangements of silicon and carbon atoms as concluded from IR and Raman spectroscopy measurements carried out on the same samples. The results not only allow a correlation between film properties and deposition temperature but also support the notion of the UHV-AFM images of the amorphous surfaces being atomically resolved.

  9. Bioreversible Derivatives of Phenol. 2. Reactivity of Carbonate Esters with Fatty Acid-like Structures Towards Hydrolysis in Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Claus Larsen

    2007-10-01

    Full Text Available A series of model phenol carbonate ester prodrugs encompassing derivatives with fatty acid-like structures were synthesized and their stability as a function of pH (range 0.4 – 12.5 at 37°C in aqueous buffer solutions investigated. The hydrolysis rates in aqueous solutions differed widely, depending on the selected pro-moieties (alkyl and aryl substituents. The observed reactivity differences could be rationalized by the inductive and steric properties of the substituent groups when taking into account that the mechanism of hydrolysis may change when the type of pro-moiety is altered, e.g. n-alkyl vs. t-butyl. Hydrolysis of the phenolic carbonate ester 2-(phenoxycarbonyloxy-acetic acid was increased due to intramolecular catalysis, as compared to the derivatives synthesized from ω-hydroxy carboxylic acids with longer alkyl chains. The carbonate esters appear to be less reactive towards specific acid and base catalyzed hydrolysis than phenyl acetate. The results underline that it is unrealistic to expect that phenolic carbonate ester prodrugs can be utilized in ready to use aqueous formulations. The stability of the carbonate ester derivatives with fatty acid-like structures, expected to interact with the plasma protein human serum albumin, proved sufficient for further in vitro and in vivo evaluation of the potential of utilizing HSA binding in combination with the prodrug approach for optimization of drug pharmacokinetics.

  10. ATOMIC FORCE LITHOGRAPHY OF NANO/MICROFLUIDIC CHANNELS FOR VERIFICATION AND MONITORING OF AQUEOUS SOLUTIONS

    Energy Technology Data Exchange (ETDEWEB)

    Mendez-Torres, A.; Torres, R.; Lam, P.

    2011-07-15

    The growing interest in the physics of fluidic flow in nanoscale channels, as well as the possibility for high sensitive detection of ions and single molecules is driving the development of nanofluidic channels. The enrichment of charged analytes due to electric field-controlled flow and surface charge/dipole interactions along the channel can lead to enhancement of sensitivity and limits-of-detection in sensor instruments. Nuclear material processing, waste remediation, and nuclear non-proliferation applications can greatly benefit from this capability. Atomic force microscopy (AFM) provides a low-cost alternative for the machining of disposable nanochannels. The small AFM tip diameter (< 10 nm) can provide for features at scales restricted in conventional optical and electron-beam lithography. This work presents preliminary results on the fabrication of nano/microfluidic channels on polymer films deposited on quartz substrates by AFM lithography.

  11. Investigation of hexagonal boron nitride as an atomically thin corrosion passivation coating in aqueous solution

    Science.gov (United States)

    Zhang, Jing; Yang, Yingchao; Lou, Jun

    2016-09-01

    Hexagonal boron nitride (h-BN) atomic layers were utilized as a passivation coating in this study. A large-area continuous h-BN thin film was grown on nickel foil using a chemical vapor deposition method and then transferred onto sputtered copper as a corrosion passivation coating. The corrosion passivation performance in a Na2SO4 solution of bare and coated copper was investigated by electrochemical methods including cyclic voltammetry (CV), Tafel polarization and electrochemical impedance spectroscopy (EIS). CV and Tafel analysis indicate that the h-BN coating could effectively suppress the anodic dissolution of copper. The EIS fitting result suggests that defects are the dominant leakage source on h-BN films, and improved anti-corrosion performances could be achieved by further passivating these defects.

  12. Carbon nanotubes dispersed in aqueous solution by ruthenium(ii) polypyridyl complexes

    Science.gov (United States)

    Huang, Kewei; Saha, Avishek; Dirian, Konstantin; Jiang, Chengmin; Chu, Pin-Lei E.; Tour, James M.; Guldi, Dirk M.; Martí, Angel A.

    2016-07-01

    Cationic ruthenium(ii) polypyridyl complexes with appended pyrene groups have been synthesized and used to disperse single-walled carbon nanotubes (SWCNT) in aqueous solutions. To this end, planar pyrene groups enable association by means of π-stacking onto carbon nanotubes and, in turn, the attachment of the cationic ruthenium complexes. Importantly, the ionic nature of the ruthenium complexes allows the formation of stable dispersions featuring individualized SWCNTs in water as confirmed in a number of spectroscopic and microscopic assays. In addition, steady-state photoluminescence spectroscopy was used to probe the excited state interactions between the ruthenium complexes and SWCNTs. These studies show that the photoluminescence of both, that is, of the ruthenium complexes and of SWCNTs, are quenched when they interact with each other. Pump-probe transient absorption experiments were performed to shed light onto the nature of the photoluminescence quenching, showing carbon nanotube-based bands with picosecond lifetimes, but no new bands which could be unambigously assigned to photoinduced charge transfer process. Thus, from the spectroscopic data, we conclude that quenching of the photoluminescence of the ruthenium complexes is due to energy transfer to proximal SWCNTs.Cationic ruthenium(ii) polypyridyl complexes with appended pyrene groups have been synthesized and used to disperse single-walled carbon nanotubes (SWCNT) in aqueous solutions. To this end, planar pyrene groups enable association by means of π-stacking onto carbon nanotubes and, in turn, the attachment of the cationic ruthenium complexes. Importantly, the ionic nature of the ruthenium complexes allows the formation of stable dispersions featuring individualized SWCNTs in water as confirmed in a number of spectroscopic and microscopic assays. In addition, steady-state photoluminescence spectroscopy was used to probe the excited state interactions between the ruthenium complexes and SWCNTs

  13. Changes on the nanostructure of cementitius calcium silicate hydrates (C-S-H) induced by aqueous carbonation

    OpenAIRE

    Morales-Florez, Víctor; Findling, N.; F. Brunet

    2015-01-01

    The nanostructure of the main binding phase of the hydrated cements, the calcium silicate hydrates (C-S-H), and their structural changes due to aqueous carbonation have been characterized using TEM, nitrogen physisorption, and SAXS. Synthetic C-S-H has been used for this purpose. Two different morphologies were identified, similar to the high density and low density C-S-H types. When submitting the sample to a CO 2 flux, the low density phase was completely carbonated. The carbonation by-prod...

  14. PREFACE: 8th Asian International Seminar on Atomic and Molecular Physics (AISAMP)

    Science.gov (United States)

    Williams, Jim F.; Buckman, Steve; Bieske, Evan J.

    2009-09-01

    These proceedings arose from the 8th Asian International Seminar on Atomic and Molecular Physics (AISAMP) which was held at the University of Western Australia 24-28 November 2008. The history of AISAMP (Takayanagi and Matsuzawa 2002) recognizes its origin from the Japan-China meeting of 1985, and the first use of the name 'The First Asian International Seminar on Atomic and Molecular Physics (AISAMP)' in 1992. The initial attendees, Japan and China, were joined subsequently by scientists from Korea, Taiwan, India, Australia and recently by Malaysia, Thailand, Vietnam, Turkey Iran, UK and USA. The main purpose of the biennial AISAMP series is to create a wide forum for exchanging ideas and information among atomic and molecular scientists and to promote international collaboration. The scope of the AISAMP8 meeting included pure, strategic and applied research involving atomic and molecular structure and processes in all forms of matter and antimatter. For 2008 the AISAMP conference incorporated the Australian Atomic and Molecular Physics and Quantum Chemistry meeting. The topics for AISAMP8 embraced themes from earlier AISAMP meetings and reflected new interests, in atomic and molecular structures, spectroscopy and collisions; atomic and molecular physics with laser or synchrotron radiation; quantum information processing using atoms and molecules; atoms and molecules in surface physics, nanotechnology, biophysics, atmospheric physics and other interdisciplinary studies. The implementation of the AISAMP themes, as well as the international representation of research interests, is indicated both in the contents list of these published manuscripts as well as in the program for the meeting. Altogether, 184 presentations were made at the 8th AISAMP, including Invited Talks and Contributed Poster Presentations, of which 60 appear in the present Proceedings after review by expert referees in accordance with the usual practice of Journal of Physics: Conference Series of

  15. Nuclear techniques in food and agriculture. 1980-1994. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    The catalogue lists all publications of the International Atomic Energy Agency dealing with Food And Agriculture during the period 1980-1994. The major subjects covered include: food irradiation, insect and pest control, mutation plant breeding, plant biotechnology, soil fertility and irrigation, agrochemicals animal production and health

  16. Nuclear power. Nuclear fuel cycle and waste management. 1990-2002. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This document lists all sales publications of the International Atomic Energy Agency dealing with Nuclear Power, Nuclear Fuel Cycle and Waste Management, issued during the period 1990-2002. It gives a short abstract of these publications along with contents and their costs

  17. The role of international atomic energy agency in maintaining nuclear safety competence

    International Nuclear Information System (INIS)

    This paper provides information how International Atomic Energy Agency can assist Member States in maintaining and developing nuclear safety competence. The topics covered include the development of safety standards, organisation of nuclear safety related conferences, provision of safety reviews, organisation of training courses and topical workshops and publication of training related documents. Usefulness of these activities for competence development is discussed. (author)

  18. Transport of radioactive material. 1994-2002. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This document lists all sales publications, IAEA-TECDOC Series, Training Course Series and National Competent Authorities Lists of the International Atomic Energy Agency dealing with the transport of radioactive materials during the period 1994-2002. It gives a short abstract and contents of these issues along with their costs in EURO

  19. Arsenate removal from aqueous solution by cellulose-carbonated hydroxyapatite nanocomposites

    International Nuclear Information System (INIS)

    Microwave-assisted synthesis of the cellulose-carbonated hydroxyapatite nanocomposites (CCHA) with CHA nanostructures dispersed in the cellulose matrix was carried out by using cellulose solution, CaCl2, and NaH2PO4. The cellulose solution was previously prepared by the dissolution of microcrystalline cellulose in NaOH-urea aqueous solution. Study was carried out to evaluate the feasibility of synthetic CCHA for As(V) removal from aqueous solution. Batch experiments were performed to investigate effects of various experimental parameters such as contact time (5 min - 8 h), initial As(V) concentration (1-50 mg/L), temperature (25, 35 and 45 oC), pH (2-10) and the presence of competing anions on As(V) adsorption on the synthetic CCHA. Kinetic data reveal that the uptake rate of As(V) was rapid at the beginning and equilibrium was achieved within 1 h. The adsorption process was well described by pseudo-first-order kinetics model. The adsorption data better fitted Langmuir isotherm. The maximum adsorption capacity calculated from Langmuir isotherm model was up to 12.72 mg/g. Thermodynamic study indicates an endothermic nature of adsorption and a spontaneous and favorable process. The optimum pH for As(V) removal was broad, ranging from 4 to 8. The As(V) adsorption was impeded by the presence of SiO32-, followed by PO43- and NO3-. The adsorption process appeared to be controlled by the chemical process.

  20. Batch, Kinetic and Equilibrium Studies of Chromium (Vi From Aqueous Phase Using Activated Carbon Derived From Lantana Camara Fruit

    Directory of Open Access Journals (Sweden)

    K. Nithya

    2015-12-01

    Full Text Available Batch experiments have been conducted to determine the maximum adsorption capacity of activated carbon derived from Lantana camara fruit to remove hexavalent chromium from aqueous solution. The removal efficiency and uptake capacity of the biosorbent were determined by varying several batch level parameters. Highest removal efficiency of the biosorbent was found to be almost 99% under optimal conditions. Maximum monolayer adsorption capacity was determined to be 86 mg/g. The experimental data best fitted with Langmuir adsorption isotherm and pseudo second order model. These findings conclude that the selected biosorbent has more promising features in binding hexavalent chromium in aqueous media.

  1. Current-induced dynamics in carbon atomic contacts

    DEFF Research Database (Denmark)

    Lu, Jing Tao; Gunst, Tue; Brandbyge, Mads;

    2011-01-01

    Background: The effect of electric current on the motion of atoms still poses many questions, and several mechanisms are at play. Recently there has been focus on the importance of the current-induced nonconservative forces (NC) and Berry-phase derived forces (BP) with respect to the stability of...

  2. Molecular dynamics simulation for arrangement of nickel atoms filled in carbon nanotubes

    International Nuclear Information System (INIS)

    Carbon Nanotubes (CNTs) filled with metals can be used in capacitors, sensors, rechargeable batteries, and so on. Atomic arrangement of the metals has an important role in the function of the composites. The tips of CNTs were opened, and then nickel was filled by means of hydrothermal oxidation/ultrasonic vibration method. The tests of TEM, HREM, and EDX (energy-dispersive X-ray spectroscopy) analysis showed that Ni was filled in CNTs successfully. The atomic arrangement of nickel filled into single wall carbon nanotubes was investigated by molecular dynamics simulation. The radial distribution function and bond orientation order were established to analyze the atomic arrangement of nickel filled in carbon nanotubes during the cooling process. The results show that nickel atoms became in order gradually and preferably crystallized on the inner wall of carbon nanotubes when the temperature decreased from 1600 K. After it cooled to 100 K, the arrangement of nickel atoms in outermost circle was regular and dense, but there were many defects far from the wall of CNTs. According to the calculation of bond orientation order parameters Q6 and its visualization, the structure of nickel is Face-centered cube (f.c.c). (1,1,1)Ni was close on the inner surface of carbon nanotubes. Radial direction of CNTs was [1,1,1] crystal orientation. Axial direction of CNTs, namely, filling direction, was [1¯, 1¯,2] crystal orientation

  3. Carbon Dioxide Management on the International Space Station

    Science.gov (United States)

    Burlingame, Katie

    2016-01-01

    The International Space Station (ISS) is a manned laboratory operating in orbit around the Earth that was built and is currently operated by several countries across the world. The ISS is a platform for novel scientific research as well as a testbed for technologies that will be required for the next step in space exploration. In order for astronauts to live on ISS for an extended period of time, it is vital that on board systems consistently provide a clean atmosphere. One contaminant that must be removed from the atmosphere is carbon dioxide (CO2). CO2 levels on ISS are higher than those on Earth and can cause crew members to experience symptoms such as headaches, lethargy and mental slowness. A variety of systems exist on ISS to remove carbon dioxide, including adsorbent technologies which can be reused and testbed technologies for future space vehicles.

  4. Application of carbonated apatite coating on a Ti substrate by aqueous spray method

    Energy Technology Data Exchange (ETDEWEB)

    Mochizuki, Chihiro; Hara, Hiroki [Division of Liberal Arts, Kogakuin University, 2665-1, Nakano, Hachioji, Tokyo 192-0015 (Japan); Takano, Ichiro [Department of Electrical Engineering, Kogakuin University, 2665-1, Nakano, Hachioji, Tokyo 192-0015 (Japan); Hayakawa, Tohru [Department of Dental Engineering, Tsurumi University School of Dental Medicine, Tsurumi, Yokohama City, Kanagawa 230-8501 (Japan); Sato, Mitsunobu, E-mail: lccsato@cc.kogakuin.ac.jp [Division of Liberal Arts, Kogakuin University, 2665-1, Nakano, Hachioji, Tokyo 192-0015 (Japan)

    2013-03-01

    The fabrication and characterization of a carbonate-containing apatite film deposited on a Ti plate via an aqueous spray method is described. The mist of the spray solution emitted from a perpendicularly oriented airbrush was made to strike a warmed Ti substrate. The thicknesses of the sprayed film and those heat-treated at 400 Degree-Sign C-700 Degree-Sign C under Ar gas flow were in the range 1.21-1.40 {mu}m. The results of elemental analyses and Fourier transform infrared spectroscopy of the powders that were mechanically collected from the surface of the sprayed film suggest that the film was Ca{sub 10}(PO{sub 4})6(CO{sub 3}) {center_dot} 2CO{sub 2} {center_dot} 3H{sub 2}O. The presence of the carbonate ion and the lattice CO{sub 2} molecule was confirmed via the aforementioned analyses; the finding was also consistent with the X-ray diffraction patterns of the films and the chemical identity of the sprayed and heat-treated films that were measured using X-ray photoelectron spectroscopy. The sprayed film comprises a characteristic network structure, which contains round particles within the networks, as was observed by field-emission scanning electron microscopy. A scratch test indicated that the shear stress of the sprayed film (21 MPa) significantly improved to 40 and > 133 MPa after heat-treatment at 600 Degree-Sign C and 700 Degree-Sign C, respectively, under Ar gas flow for 10 min. - Highlights: Black-Right-Pointing-Pointer CO{sub 2} inserted CA films were fabricated on a Ti plate by the aqueous spray method. Black-Right-Pointing-Pointer The characteristic network structure of the sprayed film was clarified by FE-SEM. Black-Right-Pointing-Pointer Ca{sub 10}(PO{sub 4})6(CO{sub 3}) {center_dot} 2CO{sub 2} {center_dot} 3H{sub 2}O film with a thickness of ca. 1 {mu}m could be deposited. Black-Right-Pointing-Pointer A well-adhered film with shear stress of 21 MPa was obtained at low temperatures. Black-Right-Pointing-Pointer A stable solution for VOC

  5. Application of carbonated apatite coating on a Ti substrate by aqueous spray method

    International Nuclear Information System (INIS)

    The fabrication and characterization of a carbonate-containing apatite film deposited on a Ti plate via an aqueous spray method is described. The mist of the spray solution emitted from a perpendicularly oriented airbrush was made to strike a warmed Ti substrate. The thicknesses of the sprayed film and those heat-treated at 400 °C–700 °C under Ar gas flow were in the range 1.21–1.40 μm. The results of elemental analyses and Fourier transform infrared spectroscopy of the powders that were mechanically collected from the surface of the sprayed film suggest that the film was Ca10(PO4)6(CO3) · 2CO2 · 3H2O. The presence of the carbonate ion and the lattice CO2 molecule was confirmed via the aforementioned analyses; the finding was also consistent with the X-ray diffraction patterns of the films and the chemical identity of the sprayed and heat-treated films that were measured using X-ray photoelectron spectroscopy. The sprayed film comprises a characteristic network structure, which contains round particles within the networks, as was observed by field-emission scanning electron microscopy. A scratch test indicated that the shear stress of the sprayed film (21 MPa) significantly improved to 40 and > 133 MPa after heat-treatment at 600 °C and 700 °C, respectively, under Ar gas flow for 10 min. - Highlights: ► CO2 inserted CA films were fabricated on a Ti plate by the aqueous spray method. ► The characteristic network structure of the sprayed film was clarified by FE-SEM. ► Ca10(PO4)6(CO3) · 2CO2 · 3H2O film with a thickness of ca. 1 μm could be deposited. ► A well-adhered film with shear stress of 21 MPa was obtained at low temperatures. ► A stable solution for VOC-free spraying was facilely prepared.

  6. Hope over fear. The establishment of the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    President Eisenhower's ''Atoms for Peace'' speech in 1953 started a process that led to the establishment of the International Atomic Energy Agency (IAEA). This study analyses the negotiations of the Statute of the Agency. It focuses on how the Agency's scope of action regarding safeguards was negotiated. The Statute is seen as a reflection of the dual purpose of the new Agency to promote peaceful uses of nuclear energy, and to control that peaceful nuclear activities receiving IAEA assistance are not diverted to military purposes. On one hand, the countries receiving assistance from the Agency accepted a degree of international control that represented a breakthrough in international relations. On the other hand, many countries strongly resented controls. Consequently, compromises had to be made in the course of the negotiations in order to reach a consensus. Thus, although the IAEA was established as a competent and technical body, the underlying compromises meant that its scope of actions was restricted. 6 refs

  7. Development of a Rapid, Nondestructive Method to Measure Aqueous Carbonate in High Salinity Brines Using Raman Spectroscopy

    Science.gov (United States)

    McGraw, L.; Phillips-Lander, C. M.; Elwood Madden, A. S.; Parnell, S.; Elwood Madden, M.

    2015-12-01

    Traditional methods of quantitative analysis are often ill-suited to determining the bulk chemistry of high salinity brines due to their corrosive and clogging properties. Such methods are also often difficult to apply remotely in planetary environments. However, Raman spectroscopy can be used remotely without physical contact with the fluid and is not affected by many ionic brines. Developing methods to study aqueous carbonates is vital to future study of brines on Mars and other planetary bodies, as they can reveal important information about modern and ancient near-surface aqueous processes. Both sodium carbonate standards and unknown samples from carbonate mineral dissolution experiments in high salinity brines were analyzed using a 532 nm laser coupled to an inVia Renishaw spectrometer to collect carbonate spectra from near-saturated sodium chloride and sodium sulfate brines. A calibration curve was determined by collecting spectra from solutions of known carbonate concentrations mixed with a pH 13 buffer and a near-saturated NaCl or Na2SO4 brine matrix. The spectra were processed and curve fitted to determine the height ratio of the carbonate peak at 1066 cm-1 to the 1640 cm-1 water peak. The calibration curve determined using the standards was then applied to the experimental data after accounting for dilutions. Concentrations determined based on Raman spectra were compared against traditional acid titration measurements. We found that the two techniques vary by less than one order of magnitude. Further work is ongoing to verify the method and apply similar techniques to measure aqueous carbonate concentrations in other high salinity brines.Traditional methods of quantitative analysis are often ill-suited to determining the bulk chemistry of high salinity brines due to their corrosive and clogging properties. Such methods are also often difficult to apply remotely in planetary environments. However, Raman spectroscopy can be used remotely without physical

  8. Ultra-Low-Temperature Reactions of Carbon Atoms with Hydrogen Molecules

    CERN Document Server

    Krasnokutski, S A; Renzler, M; Jäger, C; Henning, Th; Scheier, P

    2016-01-01

    The reactions of carbon atoms with dihydrogen have been investigated in liquid helium droplets at $T$ = 0.37 K. A calorimetric technique was applied to monitor the energy released in the reaction. The barrierless reaction between a single carbon atom and a single dihydrogen molecule was detected. Reactions between dihydrogen clusters and carbon atoms have been studied by high-resolution mass spectrometry. The formation of hydrocarbon cations of the type C$_m$H$_n^+$, with $m$ = 1-4 and $n$ = 1-15 was observed. With enhanced concentration of dihydrogen, the mass spectra demonstrated the main "magic" peak assigned to the CH$_5^+$ cation. A simple formation pathway and the high stability of this cation suggest its high abundance in the interstellar medium.

  9. Weighing a single atom using a coupled plasmon–carbon nanotube system

    Directory of Open Access Journals (Sweden)

    Jin-Jin Li and Ka-Di Zhu

    2012-01-01

    Full Text Available We propose an optical weighing technique with a sensitivity down to a single atom, using a surface plasmon and a doubly clamped carbon nanotube resonator. The mass of a single atom is determined via the vibrational frequency shift of the carbon nanotube while the atom attaches to the nanotube surface. Owing to the ultralight mass and high quality factor of the carbon nanotube, and the spectral enhancement by the use of surface plasmon, this method results in a narrow linewidth (kHz and high sensitivity (2.3×10−28 Hzcenterdot g−1, which is five orders of magnitude more sensitive than traditional electrical mass detection techniques.

  10. Stabilization of carbon dioxide (CO2) bubbles in micrometer-diameter aqueous droplets and the formation of hollow microparticles.

    Science.gov (United States)

    Lu, Tianyi; Fan, Rong; Delgadillo, Luis F; Wan, Jiandi

    2016-04-26

    We report an approach to stabilize carbon dioxide (CO2) gas bubbles encapsulated in micrometer-diameter aqueous drops when water in the aqueous drops is evaporated. CO2-in-water-in-oil double emulsion drops are generated using microfluidic approaches and evaporation is conducted in the presence of sodium dodecyl sulfate (SDS), poly(vinyl alcohol) (PVA) and/or graphene oxide (GO) particles dispersed in the aqueous phase of the double emulsion drops. We examine the roles of the bubble-to-drop size ratio, PVA and GO concentration in the stabilization of CO2 bubbles upon water evaporation and show that thin-shell particles with encapsulated CO2 bubbles can be obtained under optimized conditions. The developed approach offers a new strategy to study CO2 dissolution and stability on the microscale and the synthesis of novel gas-core microparticles. PMID:27025654

  11. Selective Separation of Trivalent Actinides from Lanthanides by Aqueous Processing with Introduction of Soft Donor Atoms

    International Nuclear Information System (INIS)

    Implementation of a closed loop nuclear fuel cycle requires the utilization of Pu-containing MOX fuels with the important side effect of increased production of the transplutonium actinides, most importantly isotopes of Am and Cm. Because the presence of these isotopes significantly impacts the long-term radiotoxicity of high level waste, it is important that effective methods for their isolation and/or transmutation be developed. Furthermore, since transmutation is most efficiently done in the absence of lanthanide fission products (high yield species with large thermal neutron absorption cross sections) it is important to have efficient procedures for the mutual separation of Am and Cm from the lanthanides. The chemistries of these elements are nearly identical, differing only in the slightly stronger strength of interaction of trivalent actinides with ligand donor atoms softer than O (N, Cl-, S). Research being conducted around the world has led to the development of new reagents and processes with considerable potential for this task. However, pilot scale testing of these reagents and processes has demonstrated the susceptibility of the new classes of reagents to radiolytic and hydrolytic degradation. In this project, separations of trivalent actinides from fission product lanthanides have been investigated in studies of (1) the extraction and chemical stability properties of a class of soft-donor extractants that are adapted from water-soluble analogs, (2) the application of water soluble soft-donor complexing agents in tandem with conventional extractant molecules emphasizing fundamental studies of the TALSPEAK Process. This research was conducted principally in radiochemistry laboratories at Washington State University. Collaborators at the Radiological Processing Laboratory (RPL) at the Pacific Northwest National Laboratory (PNNL) have contributed their unique facilities and capabilities, and have supported student internships at PNNL to broaden their

  12. Selective Separation of Trivalent Actinides from Lanthanides by Aqueous Processing with Introduction of Soft Donor Atoms

    Energy Technology Data Exchange (ETDEWEB)

    Kenneth L. Nash

    2009-09-22

    Implementation of a closed loop nuclear fuel cycle requires the utilization of Pu-containing MOX fuels with the important side effect of increased production of the transplutonium actinides, most importantly isotopes of Am and Cm. Because the presence of these isotopes significantly impacts the long-term radiotoxicity of high level waste, it is important that effective methods for their isolation and/or transmutation be developed. Furthermore, since transmutation is most efficiently done in the absence of lanthanide fission products (high yield species with large thermal neutron absorption cross sections) it is important to have efficient procedures for the mutual separation of Am and Cm from the lanthanides. The chemistries of these elements are nearly identical, differing only in the slightly stronger strength of interaction of trivalent actinides with ligand donor atoms softer than O (N, Cl-, S). Research being conducted around the world has led to the development of new reagents and processes with considerable potential for this task. However, pilot scale testing of these reagents and processes has demonstrated the susceptibility of the new classes of reagents to radiolytic and hydrolytic degradation. In this project, separations of trivalent actinides from fission product lanthanides have been investigated in studies of 1) the extraction and chemical stability properties of a class of soft-donor extractants that are adapted from water-soluble analogs, 2) the application of water soluble soft-donor complexing agents in tandem with conventional extractant molecules emphasizing fundamental studies of the TALSPEAK Process. This research was conducted principally in radiochemistry laboratories at Washington State University. Collaborators at the Radiological Processing Laboratory (RPL) at the Pacific Northwest National Laboratory (PNNL) have contributed their unique facilities and capabilities, and have supported student internships at PNNL to broaden their

  13. Central atom/substituent effects onmagnetothermal properties of metal porphyrins in aqueous suspension

    Energy Technology Data Exchange (ETDEWEB)

    Lomova, T.N., E-mail: tnl@isc-ras.ru; Korolev, V.V.; Zakharov, A.G.

    2014-08-01

    Highlights: • Magnetothermal properties of Mn/Ln(III) porphyrins were obtained by microcalorimetry. • (AcO)GdTPP shows giant magnetocaloric effect compared to La{sub 0.8}Ag{sub 0.15}MnO{sub 3}. • Mn porphyrins’ heat capacities depend on induction with a maximum at 0.25–0.35 T. • Dependences of MCE on molecules structure were determined for the first time. • We explored the prospects of using metal porphyrin magnetothermal properties for various applications. - Abstract: Magnetothermal properties of (X)Mn{sup III}P and (X)Ln{sup III}P, where X = chloro-, bromo-, acetate-ligand; Ln = Eu, Gd, Tm and P = (2,3,7,8,12,13,17,18-octaethylporphyrinato)-, (5,10,15,20-tetraphenylporphyrinato)- or (2,3,7,8,12,13,17, 18-octa-para-tert-butylphenyltetraazaporphyrinato)-ligand, as 6% water suspensions were determined by the microcalorimetric method at 298–353 K in a magnetic induction of 0–1.0 T. High-disperse complex particles were found to have paramagnetic properties. It was established that positive MCE increases with an increase in magnetic induction at all temperatures and decreases with an increase in temperature at all magnetic inductions; in the case of (Cl)GdTPP actually MCE does not depend on temperature. Dependences of specific heat capacity and that of the change in enthalpy and magnetic entropy of the studied complexes on magnetic induction were explored. The first of these dependencies has a maximum at 0.25–0.35 T at all temperatures. Heat capacity of the lanthanide complexes slightly increases with an increase in temperature; a magnetic component of heat capacity takes place only in (AcO)GdTPP at temperatures above 298 K. The regularities of the influence of central atom, acidoligand and a macrocycle composition in porphyrin complexes on their magnetothermal properties were established. Both a macrocycle composition in the case of manganese complexes and an acidoligand variation in the case of lanthanide complexes are bigger than the other

  14. Carbon nanotube synthesis: from large-scale production to atom-by-atom growth

    International Nuclear Information System (INIS)

    The extraordinary electronic, thermal and mechanical properties of carbon nanotubes (CNTs) closely relate to their structure. They can be seen as rolled-up graphene sheets with their electronic properties depending on how this rolling up is achieved. However, this is not the way they actually grow. Various methods are used to produce carbon nanotubes. They all have in common three ingredients: (i) a carbon source, (ii) catalyst nanoparticles and (iii) an energy input. In the case where the carbon source is provided in solid form, one speaks about ‘high temperature methods’ because they involve the sublimation of graphite which does not occur below 3200 °C. The first CNTs were synthesized by these techniques. For liquid or gaseous phases, the generic term of ‘medium or low temperature methods’ is used. CNTs are now commonly produced by these latter techniques at temperatures ranging between 350 and 1000 °C, using metal nanoparticles that catalyze the decomposition of the gaseous carbon precursor and make the growth of nanotubes possible. The aim of this review article is to give a general overview of all these methods and an understanding of the CNT growth process. (topical review)

  15. Standard practice for analysis of aqueous leachates from nuclear waste materials using inductively coupled plasma-atomic emission spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This practice is applicable to the determination of low concentration and trace elements in aqueous leachate solutions produced by the leaching of nuclear waste materials, using inductively coupled plasma-atomic emission spectroscopy (ICP-AES). 1.2 The nuclear waste material may be a simulated (non-radioactive) solid waste form or an actual solid radioactive waste material. 1.3 The leachate may be deionized water or any natural or simulated leachate solution containing less than 1 % total dissolved solids. 1.4 This practice should be used by analysts experienced in the use of ICP-AES, the interpretation of spectral and non-spectral interferences, and procedures for their correction. 1.5 No detailed operating instructions are provided because of differences among various makes and models of suitable ICP-AES instruments. Instead, the analyst shall follow the instructions provided by the manufacturer of the particular instrument. This test method does not address comparative accuracy of different devices...

  16. The over-step coalescence of carbon atoms on copper surface in the CVD growth of graphene: density functional calculations

    Directory of Open Access Journals (Sweden)

    Yingfeng Li

    2013-05-01

    Full Text Available The ways in which carbon atoms coalesce over the steps on copper (111 surface are ascertained by density functional theory (DFT calculations in the context of chemical vapor deposition (CVD growth of graphene. Two strategies, (1 by putting carbon atoms on and under the steps separately and (2 by importing additional carbon atoms between the ones separated by the steps, have been attempted to investigate if an over-step coalescence of carbon atoms could take place. Based on analyses about the optimized configurations and adsorption energies of carbon atoms nearby the steps, as well as the energy evolution curve of the system throughout the geometry optimizations process, we determined the main way in which graphene grows over the steps continuously: the carbon atoms, adsorbed additionally on the locations between the already existing ones which are separated by the steps, link them (these carbon atoms separated by the steps together. The direct over-step coalescence of the carbon atoms separated by the steps is very difficult, although the energy barrier preventing their coalescence can be weakened by importing carbon atoms on and under the steps gradually. Our results imply potential applications in directing the fabrication of graphene with particular structure by controlling the surface topography of copper substrate.

  17. A green heterogeneous synthesis of N-doped carbon dots and their photoluminescence applications in solid and aqueous states

    Science.gov (United States)

    Xu, Minghan; He, Guili; Li, Zhaohui; He, Fengjiao; Gao, Feng; Su, Yanjie; Zhang, Liying; Yang, Zhi; Zhang, Yafei

    2014-08-01

    Compared with traditional semiconductor quantum dots (QDs) and organic dyes, photoluminescent carbon dots (CDs) are superior because of their high aqueous solubility, robust chemical inertness, facile functionalization, high resistance to photobleaching, low toxicity and good biocompatibility. Herein, a green, large-scale and high-output heterogeneous synthesis of N-doped CDs was developed by reacting calcium citrate and urea under microwave irradiation without the use of any capping agents. The obtained N-doped CDs with a uniform size distribution exhibit good aqueous solubility and yellowish-green fluorescence in the solid and aqueous states. These unique luminescence properties of N-doped CDs inspire new thoughts for applications as fluorescent powders, fluorescent inks, the growth of fluorescent bean sprouts, and fingerprint detection tools.Compared with traditional semiconductor quantum dots (QDs) and organic dyes, photoluminescent carbon dots (CDs) are superior because of their high aqueous solubility, robust chemical inertness, facile functionalization, high resistance to photobleaching, low toxicity and good biocompatibility. Herein, a green, large-scale and high-output heterogeneous synthesis of N-doped CDs was developed by reacting calcium citrate and urea under microwave irradiation without the use of any capping agents. The obtained N-doped CDs with a uniform size distribution exhibit good aqueous solubility and yellowish-green fluorescence in the solid and aqueous states. These unique luminescence properties of N-doped CDs inspire new thoughts for applications as fluorescent powders, fluorescent inks, the growth of fluorescent bean sprouts, and fingerprint detection tools. Electronic supplementary information (ESI) available: The photos of different precursors under daylight and 365 nm UV beam; 1H-NMR and Raman spectrum of N-doped CDs; toxicity study of bean sprouts; the correlation between length of bean sprouts and the concentration of N-doped CDs

  18. A simple synthesis method to produce metal oxide loaded carbon paper using bacterial cellulose gel and characterization of its electrochemical behavior in an aqueous electrolyte

    Science.gov (United States)

    Miyajima, Naoya; Jinguji, Ken; Matsumura, Taiyu; Matsubara, Toshihiro; Sakane, Hideto; Akatsu, Takashi; Tanaike, Osamu

    2016-04-01

    A simple synthetic chemical process to produce metal oxide loaded carbon papers was developed using bacterial cellulose gel, which consisted of nanometer-sized fibrous cellulose and water. Metal ions were successfully impregnated into the gel via aqueous solution media before drying and carbonization methods resulting in metal oxide contents that were easy to control through variations in the concentration of aqueous solutions. The papers loaded by molybdenum oxides were characterized as pseudocapacitor electrodes preliminary, and the large redox capacitance of the oxides was followed by a conductive fibrous carbon substrate, suggesting that a binder and carbon black additive-free electrode consisting of metal oxides and carbon paper was formed.

  19. Comparative performance of cement kiln dust and activated carbon in removal of cadmium from aqueous solutions.

    Science.gov (United States)

    El-Refaey, Ahmed A

    2016-01-01

    This study compared the performance of cement kiln dust (CKD) as industrial byproduct and commercially activated carbon (AC) as adsorbent derived from agricultural waste for the removal of cadmium (Cd(2+)) from aqueous solutions. CKD and AC were characterized by Fourier transform infrared (FTIR) and scanning electron microscopy (SEM) and surface areas demonstrate the differences of physicochemical properties. Batch equilibrium experiments were conducted for various intervals extended to 96 h at 20, 25 and 30°C to investigate the efficiency of the sorbents in the removal of Cd(2+). CKD expressed high affinity for removal of Cd(2+) and was not affected by temperature, while AC was significantly affected, which reflects dissimilarity in the retention mechanisms defendant in CKD and those pursued by AC. The results were explained by changes of FTIR and SEM images before and after sorption experiments. The suggestion is that electrostatic ion exchange and complex reactions are the main mechanisms for Cd(2+) removal. The kinetic data were evaluated by fractional power, Elovich, pseudo-first order and pseudo-second-order kinetic models. The pseudo-second-order kinetic model was found to correlate with the experimental data well. These results revealed that CKD can be used as a cost-effective and efficient sorbent for Cd(2+) removal in comparison with AC. PMID:27054742

  20. 2-chlorophenol sorption from aqueous solution using granular activated carbon and polymeric adsorbents

    Science.gov (United States)

    Ghatbandhe, A. S.; Jahagirdar, H. G.; Yenkie, M. K. N.; Deosarkar, S. D.

    2013-08-01

    Adsorption equilibrium and kinetics of 2-chlorophenol (2-CP) one of the chlorophenols (CPs) onto bituminous coal based Filtrasorb-400 grade granular activated carbon and three different types of polymeric adsorbents were studied in aqueous solution in a batch system. Langmuir isotherm models were applied to experimental equilibrium data of 2-CP adsorption. Equilibrium data fitted very well to the Langmuir equilibrium models of 2-CP. Adsorbent monolayer capacity Q Langmuir constant b and adsorption rate constants k a were evaluated. 2-CP adsorption using GAC is very rapid in the first hour of contact where 70-80% of the adsorbate is removed by GAC followed by a slow approach to equilibrium. Whereas in case of polymeric adsorbents 60-65% of the adsorbate is removed in the first 30 min which is then followed by a slow approach to equilibrium. The order of adsorption of 2-CP on different adsorbents used in the study is found to be in following order: F-400 > XAD-1180 > XAD-4 > XAD-7HP.

  1. Directing carbon nanotubes from aqueous phase to o/w interface for heavy metal uptaking.

    Science.gov (United States)

    Gao, Lili; Yin, Huayi; Mao, Xuhui; Zhu, Hua; Xiao, Wei; Wang, Dihua

    2015-09-01

    Separation and reuse of dispersed nanoparticles are major obstacles to the extensive application of nano-sized absorbents in wastewater treatment. Herein, we demonstrate the capability of directing acid-oxidized carbon nanotubes (CNTs) as the transfer vehicles of heavy metal ions from simulated wastewater. The heavy metal-loaded CNTs can be readily separated from the aqueous phase via the aggregation process at an oil/water (o/w) interface. The minimum surfactant amount to achieve 99 % transfer ratio (Tr) of 100 mg/L CNTs from water phase to o/w interface was ∼0.01 mM. The adsorption experiments showed that the removal efficiency of the divalent lead ions increased with an increase in CNT mass, and the subsequent addition of cetyltrimethylammonium bromide (CTAB) surfactant did not negatively impact the removal of soluble divalent lead species (Pb(II)). In a wide region of pH and ionic strength, both the decontamination of Pb(II) and the transfer of CNTs from water phase to o/w interface can be accomplished successively. The method presented in this study may be developed as a generic one for collecting or recycling the pollutant-loaded nano-sized absorbents. PMID:25966885

  2. Removal of Cd+2 from aqueous solutions onto polypyrrole coated reticulated vitreous carbon eletrodes

    Directory of Open Access Journals (Sweden)

    Jucelânia Tramontina

    2001-07-01

    Full Text Available The development of simple methods for removal of heavy metals from aqueous samples is a relevant field of research. In this connection, the electrodeposition of the Cd+2 ion, one of the most toxic species for animals and human beings, was investigated in aerated pH 4.8 sulfuric-sulfate solutions. In potentiostatic conditions, the maximum rate of cadmium deposition at a neutral polypyrrole (PPy0 coated reticulated vitreous carbon (RVC working electrode occurs at -3.0 V vs. the saturated calomel reference electrode (SCE. Moreover, the conversion rate depends both on the applied potential and on the mass transport regime, and, for solutions containing 10 mg L-1 of Cd2+, the highest removal efficiency achieved is 84% after 90 min of electrolysis. The concentration decay of the Cd+2 ion in the solution was monitored by anodic stripping voltammetry (ASV at a hanging mercury drop electrode. Besides, metallic cadmium deposited onto the polypyrrole modified RVC electrode was evidenced by Scanning Electron Microscopy (SEM analysis using the backscattered electron image (BEI technique and by Energy Dispersive Spectrometry (EDS.

  3. Evaluating Stability of Aqueous Multiwalled Carbon Nanotube Nanofluids by Using Different Stabilizers

    Directory of Open Access Journals (Sweden)

    Tun-Ping Teng

    2014-01-01

    Full Text Available The 0.5 wt.% multiwalled carbon nanotubes/water nanofluids (MWNFs were produced by using a two-step synthetic method with different types and concentrations of stabilizers. The static position method, centrifugal sedimentation method, zeta potential measurements, and rheological experiments were used to assess the stability of the MWNFs and to determine the optimal type and fixed MWCNTs-stabilizer concentration of stabilizer. Finally, MWNFs with different concentrations of MWCNTs were produced using the optimal type and fixed concentration ratio of stabilizer, and their stability, thermal conductivity, and pH were measured to assess the feasibility of using them in heat transfer applications. MWNFs containing SDS and SDBS with MWCNTs-stabilizer concentration ratio were 5 : 2 and 5 : 4, respectively, showed excellent stability when they were evaluated by static position, centrifugal sedimentation, zeta potential, and rheological experiments at the same time. The thermal conductivity of the MWNFs indicated that the most suitable dispersing MWNF contained SDBS. MWNFs with MWCNTs concentrations of 0.25, 0.5, and 1.0 wt.% were fabricated using an aqueous SDBS solution. In addition, the thermal conductivity of the MWNFs was found to have increased, and the thermal conductivity values were greater than that of water at 25°C by 3.20%, 8.46%, and 12.49%.

  4. Removal Mechanism of Aqueous Lead by a Novel Eco-material:Carbonate Hydroxyapatite

    Institute of Scientific and Technical Information of China (English)

    Huanyan XU; Lei YANG; Peng WANG; Yu LIU; Mingsheng PENG

    2007-01-01

    Kinetics and mechanisms on the removal of aqueous lead ion by carbonate hydroxyapatite (CHap) are investigated in the present work. Experimental results show that, in the whole pH range, the lead removal percentage increases with decreasing pH values and reaches a maximum at pH=2-3. Under some conditions,the lead residual concentration is below national integrated wastewater discharge standard, even drinking water standard. The removal behavior is a complicated non-homogeneous solid/liquid reaction, which can be described by two stages from kinetic point of view. At the earlier stage, reaction rate is so fast that its kinetic course is intricate, which requires further study. At the latter stage, the rate of reaction becomes slow and the process of reaction accords with one order reaction kinetic equation. Experimental results show that the relationship between reaction rate constant k1 and temperature T accords to Arrhenius Equation, and the activation energy of sorption (Ea) is 11.93 k J/mol and frequency factor (A) is 2.51 s-1. X-ray diffraction (XRD), scanning electron microscopy with an energy dispersive X-ray fluoresence spectrometer (SEM-EDS) and toxicity characteristic leaching procedure (TCLP) test were conducted in this work. It is indicated that the main mechanism is dissolution-precipitation, accompanying with superficial sorption.

  5. Kinetic research on the sorption of aqueous lead by synthetic carbonate hydroxyapatite.

    Science.gov (United States)

    Xu, HuanYan; Yang, Lei; Wang, Peng; Liu, Yu; Peng, MingSheng

    2008-01-01

    The sorption of aqueous lead on carbonate-hydroxyapatite (CHAp) is a complicated non-homogeneous solid/water reaction, which from the kinetic point of view has two stages. In the first stage, the reaction rate is so fast and the kinetic pathway so intricate that further research is required. In the second stage, the reaction rate slows down and the reaction process follows that of a first-order kinetic equation. Experimental results show that the relationship between the reaction rate constant k(1) and temperature T agrees with the Arrhenius equation, and that the activation energy of sorption (E(a)) is 11.93 kJ/mol and the frequency factor (A) is 2.51/s. The reaction rate constant k(1) increases with the Pb(2+) initial concentration and decreasing pH, but with increasing CHAp dosage. X-ray diffraction (XRD), scanning electron microscopy with energy dispersion spectrum (SEM-EDS) and toxicity characteristic leaching procedure (TCLP) tests indicate that the main sorption mechanism is dissolution-precipitation, in conjunction with surface sorption. PMID:17360101

  6. Surface-induced patterns from evaporating droplets of aqueous carbon nanotube dispersions

    KAUST Repository

    Zeng, Hongbo

    2011-06-07

    Evaporation of aqueous droplets of carbon nanotubes (CNTs) coated with a physisorbed layer of humic acid (HA) on a partially hydrophilic substrate induces the formation of a film of CNTs. Here, we investigate the role that the global geometry of the substrate surfaces has on the structure of the CNT film. On a flat mica or silica surface, the evaporation of a convex droplet of the CNT dispersion induces the well-known "coffee ring", while evaporation of a concave droplet (capillary meniscus) of the CNT dispersion in a wedge of two planar mica sheets or between two crossed-cylinder sheets induces a large area (>mm 2) of textured or patterned films characterized by different short- and long-range orientational and positional ordering of the CNTs. The resulting patterns appear to be determined by two competing or cooperative sedimentation mechanisms: (1) capillary forces between CNTs giving micrometer-sized filaments parallel to the boundary line of the evaporating droplet and (2) fingering instability at the boundary line of the evaporating droplet and subsequent pinning of CNTs on the surface giving micrometer-sized filaments of CNTs perpendicular to this boundary line. The interplay between substrate surface geometry and sedimentation mechanisms gives an extra control parameter for manipulating patterns of self-assembling nanoparticles at substrate surfaces. © 2011 American Chemical Society.

  7. The corrosion of carbon steel in aqueous lithium hydroxide under a hydrogen blanket

    International Nuclear Information System (INIS)

    The corrosion behavior of carbon steel in 3 and 5 mol/L aqueous solutions of lithium hydroxide at 95 degrees C under a hydrogen atmosphere was investigated in immersion tests lasting ten days. Corrosion rates were determined by wight loss, and the corrosion products were characterized by bulk chemical analysis, by light and electron microscopy, and by powder X-ray diffraction. Corrosion was uniform and the corrosion rates were moderately high (0.42 mm/y in 3 mol/L and 0.56 mm/y in 5 mol/L). The corrosion products consisted of a mixture of well-formed, octahedral crystals, and poorly crystallized masses and spherules that formed by precipitation from solution. These products formed a scale on the metal surface that continually sloughed off and afforded only minor protection. Both phases were identified as lithium-iron oxides, each possessing a disordered, non-stoichiometric structure. The predominant phase was a magnetic spinel LiFe508 and the minor phase was LiFe02. A corrosion mechanism is outlined. (2 figs., 5 tabs., 20 refs.)

  8. Effective Degradation of Aqueous Tetracycline Using a Nano-TiO2/Carbon Electrocatalytic Membrane

    Directory of Open Access Journals (Sweden)

    Zhimeng Liu

    2016-05-01

    Full Text Available In this work, an electrocatalytic membrane was prepared to degrade aqueous tetracycline (TC using a carbon membrane coated with nano-TiO2 via a sol-gel process. SEM, XRD, EDS, and XPS were used to characterize the composition and structure of the electrocatalytic membrane. The effect of operating conditions on the removal rate of tetracycline was investigated systematically. The results show that the chemical oxygen demand (COD removal rate increased with increasing residence time while it decreased with increasing the initial concentration of tetracycline. Moreover, pH had little effect on the removal of tetracycline, and the electrocatalytic membrane could effectively remove tetracycline with initial concentration of 50 mg·L−1 (pH, 3.8–9.6. The 100% tetracycline and 87.8% COD removal rate could be achieved under the following operating conditions: tetracycline concentration of 50 mg·L−1, current density of 1 mA·cm−2, temperature of 25 °C, and residence time of 4.4 min. This study provides a new and feasible method for removing antibiotics in water with the synergistic effect of electrocatalytic oxidation and membrane separation. It is evident that there will be a broad market for the application of electrocatalytic membrane in the field of antibiotic wastewater treatment.

  9. Removal of Ni2+ from Aqueous Solutions by Adsorption Onto Magnetic Multiwalled Carbon Nanotube Nanocomposite

    Directory of Open Access Journals (Sweden)

    Konicki Wojciech

    2014-06-01

    Full Text Available The removal of Ni2+ from aqueous solution by magnetic multiwalled carbon nanotube nanocomposite (MMWCNTs-C was investigated. MMWCNTs-C was characterized by X-ray Diffraction method (XRD, High-Resolution Transmission Electron Microscopy (HRTEM, surface area (BET, and Fourier Transform-Infrared Spectroscopy (FTIR. The effects of initial concentration, contact time, solution pH, and temperature on the Ni2+ adsorption onto MMWCNTs-C were studied. The Langmuir and Freundlich isotherm models were applied to fit the adsorption data. The results showed that the adsorption isotherm data were fitted well to the Langmuir isotherm model with the maximum monolayer adsorption capacity of 2.11 mg g–1. The adsorption kinetics was best described by the pseudo-second-order model. The thermodynamic parameters, such as ΔHo, ΔGo and ΔSo, were also determined and evaluated. The adsorption of Ni2+ is generally spontaneous and thermodynamically favorable. The values of ΔHo and ΔGo indicate that the adsorption of Ni2+ onto MMWCNTs-C was a physisorption process.

  10. Arsenic adsorption by polyvinyl pyrrolidone K25 coated cassava peel carbon from aqueous solution

    International Nuclear Information System (INIS)

    Sorption of arsenic from aqueous solution was carried out using polyvinyl pyrrolidone K25 coated cassava peel carbon (PVPCC). Batch experiments were conducted to determine the effect of contact time, initial concentration, pH and desorption. Batch sorption data's were fitted to Lagergren kinetic studies. Column studies were also conducted using PVPCC as adsorbent. The optimized flow rate of 2.5 mL min-1 and bed height 10 cm were used to determine the effect of metal ion concentration on removal of As(V). BDST model was applied to calculate the adsorption capacity (N0) of column. The N0 value of 2.59 x 10-5, 4.21 x 10-5, 4.05 x 10-5, 4.26 x 10-5 and 3.2 x 10-5 mg g-1 were obtained for 0.5, 1.0, 1.5, 2.0 and 2.5 mg L-1 of As(V), respectively. The batch sorption proved to be more efficient than the column sorption. The sorption of As(V) and the nature of the adsorbent was examined by Fourier transmission infrared spectroscopy (FTIR) and X-ray diffraction (XRD) studies, respectively

  11. Earth sciences: Uranium geology, exploration and mining, hydrology, 1986-1996. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with earth sciences and issued during the period of 1986-1996. These topics are mainly in the field of uranium geology, exploration and mining, isotope applications in hydrology, IAEA Yearbook 1996 on the developments in nuclear science and technology and meetings on atomic energy. Proceedings of conferences, symposia and panels of experts may contain some papers in languages other than English but all of these papers have English abstracts. The prices of books are quoted in Austrian Schillings

  12. Catalytic conversion of alcohols having at least three carbon atoms to hydrocarbon blendstock

    Energy Technology Data Exchange (ETDEWEB)

    Narula, Chaitanya K.; Davison, Brian H.

    2015-11-13

    A method for producing a hydrocarbon blendstock, the method comprising contacting at least one saturated acyclic alcohol having at least three and up to ten carbon atoms with a metal-loaded zeolite catalyst at a temperature of at least 100°C and up to 550°C, wherein the metal is a positively-charged metal ion, and the metal-loaded zeolite catalyst is catalytically active for converting the alcohol to the hydrocarbon blendstock, wherein the method directly produces a hydrocarbon blendstock having less than 1 vol % ethylene and at least 35 vol % of hydrocarbon compounds containing at least eight carbon atoms.

  13. Numerical Investigation Of The Bombardment Of A Graphene Sheet By A Beam Of Carbon Atoms

    Directory of Open Access Journals (Sweden)

    O.V. Khomenko

    2009-01-01

    Full Text Available Classical molecular dynamics simulations of the bombardment of a graphene sheet by a beam of carbon atoms are carried out. Covalent bonds in the irradiated sample are described by the Brenner potential. The approximation of elastic balls interacting with graphene via the Lennard-Jones potential is used for particles in a beam. The influence of the energy and density of irradiating carbon atoms and of the presence of a thermostat on physical processes occurring during the collisions with the sample is investigated. Energy values of the particles in a beam, which are enough for the sample destruction, are defined.

  14. Atoms

    Institute of Scientific and Technical Information of China (English)

    刘洪毓

    2007-01-01

    Atoms(原子)are all around us.They are something like the bricks (砖块)of which everything is made. The size of an atom is very,very small.In just one grain of salt are held millions of atoms. Atoms are very important.The way one object acts depends on what

  15. Analysis of Solid and Aqueous Phase Products from Hydrothermal Carbonization of Whole and Lipid-Extracted Algae

    Directory of Open Access Journals (Sweden)

    Amber Broch

    2013-12-01

    Full Text Available Microalgae have tremendous potential as a feedstock for production of liquid biofuels, particularly biodiesel fuel via transesterification of algal lipids. However, biodiesel production results in significant amounts of algal residues, or “lipid extracted algae” (LEA. Suitable utilization of the LEA residue will improve the economics of algal biodiesel. In the present study, we evaluate the hydrothermal carbonization (HTC of whole and lipid extracted algal (Spirulina maxima feedstocks in order to produce a solid biofuel (hydrochar and value-added co-products in the aqueous phase. HTC experiments were performed using a 2-L Parr reactor (batch type at 175–215 °C with a 30-min holding time. Solid, aqueous and gaseous products were analyzed using various laboratory methods to evaluate the mass and carbon balances, and investigate the existence of high value chemicals in the aqueous phase. The HTC method is effective in creating an energy dense, solid hydrochar from both whole algae and LEA at lower temperatures as compared to lignocellulosic feedstocks, and is effective at reducing the ash content in the resulting hydrochar. However, under the treatment temperatures investigated, less than 1% of the starting dry algae mass was recovered as an identified high-value chemical in the aqueous phase.

  16. Multiphoton inner-shell ionization of the carbon atom

    OpenAIRE

    Rey, H. F.; Hart, H W

    2015-01-01

    We apply time-dependent R-matrix theory to study inner-shell ionization of C atoms in ultra-short high-frequency light fields with a photon energy between 170 and 245 eV. At an intensity of 1017 W/cm2, ionization is dominated by single-photon emission of a 2l electron, with two-photon emission of a 1s electron accounting for about 2-3% of all emission processes, and two-photon emission of 2l contributing about 0.5-1%. Three-photon emission of a 1s electron is estimated to contribute about 0.0...

  17. Atomically isolated nickel species anchored on graphitized carbon for efficient hydrogen evolution electrocatalysis

    Science.gov (United States)

    Fan, Lili; Liu, Peng Fei; Yan, Xuecheng; Gu, Lin; Yang, Zhen Zhong; Yang, Hua Gui; Qiu, Shilun; Yao, Xiangdong

    2016-02-01

    Hydrogen production through electrochemical process is at the heart of key renewable energy technologies including water splitting and hydrogen fuel cells. Despite tremendous efforts, exploring cheap, efficient and durable electrocatalysts for hydrogen evolution still remains as a great challenge. Here we synthesize a nickel-carbon-based catalyst, from carbonization of metal-organic frameworks, to replace currently best-known platinum-based materials for electrocatalytic hydrogen evolution. This nickel-carbon-based catalyst can be activated to obtain isolated nickel atoms on the graphitic carbon support when applying electrochemical potential, exhibiting highly efficient hydrogen evolution performance with high exchange current density of 1.2 mA cm-2 and impressive durability. This work may enable new opportunities for designing and tuning properties of electrocatalysts at atomic scale for large-scale water electrolysis.

  18. Development of the Science Data System for the International Space Station Cold Atom Lab

    Science.gov (United States)

    van Harmelen, Chris; Soriano, Melissa A.

    2015-01-01

    Cold Atom Laboratory (CAL) is a facility that will enable scientists to study ultra-cold quantum gases in a microgravity environment on the International Space Station (ISS) beginning in 2016. The primary science data for each experiment consists of two images taken in quick succession. The first image is of the trapped cold atoms and the second image is of the background. The two images are subtracted to obtain optical density. These raw Level 0 atom and background images are processed into the Level 1 optical density data product, and then into the Level 2 data products: atom number, Magneto-Optical Trap (MOT) lifetime, magnetic chip-trap atom lifetime, and condensate fraction. These products can also be used as diagnostics of the instrument health. With experiments being conducted for 8 hours every day, the amount of data being generated poses many technical challenges, such as downlinking and managing the required data volume. A parallel processing design is described, implemented, and benchmarked. In addition to optimizing the data pipeline, accuracy and speed in producing the Level 1 and 2 data products is key. Algorithms for feature recognition are explored, facilitating image cropping and accurate atom number calculations.

  19. Quantification of tip-broadening in non-contact atomic force microscopy with carbon nanotube tips

    DEFF Research Database (Denmark)

    Meinander, Kristoffer; Jensen, Thomas N.; Simonsen, Soren B.;

    2012-01-01

    Carbon nanotube terminated atomic force microscopy (AFM) probes have been used for the imaging of 5 nm wide surface supported Pt nanoclusters by non-contact (dynamic mode) AFM in an ultra-high vacuum. The results are compared to AFM measurements done with conventional Si-tips, as well...... with geometrically limited conventional probes. Superior durability also stands out as a defining feature of carbon nanotube terminated probes, allowing them to give results with a greatly enhanced reproducibility....

  20. Adsorption of Hexavalent Chromium from Aqueous Solution Using Chemically Activated Carbon Prepared from Locally Available Waste of Bamboo (Oxytenanthera abyssinica)

    OpenAIRE

    Dula, Tamirat; Siraj, Khalid; Kitte, Shimeles Addisu

    2014-01-01

    This study reports on the adsorption of Hexavalent Chromium from aqueous solutions using activated carbon prepared from bamboo (Oxytenanthera abyssinica) waste by KOH activation heating in an electrical furnace at 1073 K for 3 hrs. Batch adsorption experiments were also carried out as a function of pH, contact time, initial concentration of the adsorbate, adsorbent dosage, and temperature of the solution. Kinetic studies of the data showed that the adsorption follows the pseudo-second-order k...

  1. The effect of deposition energy of energetic atoms on the growth and structure of ultrathin amorphous carbon films studied by molecular dynamics simulations

    KAUST Repository

    Wang, N

    2014-05-16

    The growth and structure of ultrathin amorphous carbon films was investigated by molecular dynamics simulations. The second-generation reactive-empirical-bond-order potential was used to model atomic interactions. Films with different structures were simulated by varying the deposition energy of carbon atoms in the range of 1-120 eV. Intrinsic film characteristics (e.g. density and internal stress) were determined after the system reached equilibrium. Short- and intermediate-range carbon atom ordering is examined in the context of atomic hybridization and ring connectivity simulation results. It is shown that relatively high deposition energy (i.e., 80 eV) yields a multilayer film structure consisting of an intermixing layer, bulk film and surface layer, consistent with the classical subplantation model. The highest film density (3.3 g cm-3), sp3 fraction (∼43%), and intermediate-range carbon atom ordering correspond to a deposition energy of ∼80 eV, which is in good agreement with experimental findings. © 2014 IOP Publishing Ltd.

  2. Padronização interna em espectrometria de absorção atômica Internal standardization in atomic absorption spectrometry

    OpenAIRE

    Kelly G. Fernandes; Mercedes de Moraes; José A. Gomes Neto; Joaquim A. Nóbrega; Pedro V. Oliveira

    2003-01-01

    This paper describes a review on internal standardization in atomic absorption spectrometry with emphasis to the systematic and random errors in atomic absorption spectrometry and applications of internal standardization in flame atomic absorption spectrometry and electrothermal atomic absorption spectrometry. The rules for selecting an element as internal standard, limitations of the method, and some comments about the application of internal standardization in atomic absorption spectrometry...

  3. Conversion electron Moessbauer study of low carbon steel polarized in aqueous sulfate solution containing sulfite in low concentration

    International Nuclear Information System (INIS)

    The passivation of low carbon steel was studied in aqueous solution of 0.5 M Na2SO4+0.001 M NaHSO3 at pH=3.5 and 6.5. The found major components at pH=3.5 were: γ-FeOOH and Fe3C, and also FeSO4.H2O could be identified on the surface of the low carbon steel as a minor component. At pH=6.5, the passive film contained only amorphous iron(III)-oxide or oxyhydroxide. (orig.)

  4. Atomic size-limited intercalation into single wall carbon nanotubes

    International Nuclear Information System (INIS)

    Intercalation of single wall carbon nanotubes (SWNTs) provides an important tool to modify their electronic band structure. Using multiple excitation wavelength Raman spectroscopy, we demonstrate that intercalation into SWNT interiors can be limited by intercalant size resulting in an unusual material comprising SWNTs with varying charge density. In the particular case of iodine intercalation, larger SWNTs with iodine-filled interiors were found to carry significantly higher charge density as compared to smaller empty ones. This difference was used to separate the intercalated SWNT material into fractions with homogeneous charge density

  5. Trapping of metal Atoms on nanoprotrusions of carbon nanotubes

    DEFF Research Database (Denmark)

    Shao, Lidong; Zhang, Wei; Kuhn, Luise Theil

    2013-01-01

    Nanoprotrusions on CNTs are engineered using conventional lab treatments at a low temperature. The experimental set-up of applying a mild acid treatment with sonication and base washing is based on the development of introduced defects and vacancies. Compared with previous reports realizing selec...... selective metal depositions on individual carbon nanostructures, our work achieve a selective deposition of Pd nanoparticles on nanoprotrusions of CNTs in a bulk-phase. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim....

  6. Atoms

    International Nuclear Information System (INIS)

    Completed by recent contributions on various topics (atoms and the Brownian motion, the career of Jean Perrin, the evolution of atomic physics since Jean Perrin, relationship between scientific atomism and philosophical atomism), this book is a reprint of a book published at the beginning of the twentieth century in which the author addressed the relationship between atomic theory and chemistry (molecules, atoms, the Avogadro hypothesis, molecule structures, solutes, upper limits of molecular quantities), molecular agitation (molecule velocity, molecule rotation or vibration, molecular free range), the Brownian motion and emulsions (history and general features, statistical equilibrium of emulsions), the laws of the Brownian motion (Einstein's theory, experimental control), fluctuations (the theory of Smoluchowski), light and quanta (black body, extension of quantum theory), the electricity atom, the atom genesis and destruction (transmutations, atom counting)

  7. Protocol Additional to the agreement between France, the European Atomic Energy Community and the International Atomic Energy Agency for the application of safeguards in France

    International Nuclear Information System (INIS)

    The text of the Protocol Additional to the Agreement between France, the European Atomic Energy Community and the International Atomic Energy Agency for the Application of Safeguards in France is reproduced in the Annex to this document for the information of all Members. The Additional Protocol was approved by the Board of Governors on 11 June 1998. It was signed in Vienna on 22 September 1998. Pursuant to Article 16 of the Additional Protocol, the Protocol entered into force on 30 April 2004, the date on which the Agency received written notification that the European Atomic Energy Community and France had met their respective internal requirements for entry into force

  8. The IAEA's WorldAtom Internet site: International news and information services

    International Nuclear Information System (INIS)

    The International Atomic Energy Agency (IAEA) provides news and public information services via the Internet through its WorldAtom home page. The page is accessible at www.iaea.org/worldatom. Following are brief highlights of the items available on the site by clicking Press Centre, Reference Centre, or other links: Daily Press Review: Summaries of selected news items pertaining to global nuclear developments and the IAEA's work are provided each day, drawing upon a wide range of global media sources. IAEA NewsBriefs: Regularly featured are updates about IAEA activities related to areas of safety, technology transfer, and nuclear safeguards. Meetings and training courses: News about IAEA-sponsored symposia, seminars, and other meetings, as well as information about international meetings on atomic energy sponsored by other organizations, are updated on a daily basis. Press releases and statements: All IAEA press releases and media advisories since 1995 are accessible on the site. Topical and feature pages: In-depth coverage and links to information resources within and outside the IAEA are regularly given to selected topics of high international interest involving the IAEA. IAEA publications: listings and overviews of IAEA technical reports, safety standards, and other publications are updated as they are issued. Scientific and technical information: WorldAtom includes links (Reference Centre) to the International Nuclear Information System, IAEA's extensive bibliographic database of references and resources, to the nuclear database, and to departmental pages at IAEA that focus on IAEA programs and activities. IAEA documents: Electronic versions of official IAEA documents are added as they are issued. These documents include the texts and status lists of international conventions under IAEA auspices; IAEA information circulars to member states; IAEA annual reports (since 1995); and background reports and documents for the IAEA General Conference related to

  9. The IAEA's WorldAtom Internet site: International news and information services

    Energy Technology Data Exchange (ETDEWEB)

    Kyd, D.R.

    2000-07-01

    The International Atomic Energy Agency (IAEA) provides news and public information services via the Internet through its WorldAtom home page. The page is accessible at www.iaea.org/worldatom. Following are brief highlights of the items available on the site by clicking Press Centre, Reference Centre, or other links: Daily Press Review: Summaries of selected news items pertaining to global nuclear developments and the IAEA's work are provided each day, drawing upon a wide range of global media sources. IAEA NewsBriefs: Regularly featured are updates about IAEA activities related to areas of safety, technology transfer, and nuclear safeguards. Meetings and training courses: News about IAEA-sponsored symposia, seminars, and other meetings, as well as information about international meetings on atomic energy sponsored by other organizations, are updated on a daily basis. Press releases and statements: All IAEA press releases and media advisories since 1995 are accessible on the site. Topical and feature pages: In-depth coverage and links to information resources within and outside the IAEA are regularly given to selected topics of high international interest involving the IAEA. IAEA publications: listings and overviews of IAEA technical reports, safety standards, and other publications are updated as they are issued. Scientific and technical information: WorldAtom includes links (Reference Centre) to the International Nuclear Information System, IAEA's extensive bibliographic database of references and resources, to the nuclear database, and to departmental pages at IAEA that focus on IAEA programs and activities. IAEA documents: Electronic versions of official IAEA documents are added as they are issued. These documents include the texts and status lists of international conventions under IAEA auspices; IAEA information circulars to member states; IAEA annual reports (since 1995); and background reports and documents for the IAEA General Conference related

  10. Improved spin squeezing of an atomic ensemble through internal state control

    Science.gov (United States)

    Hemmer, Daniel; Montano, Enrique; Deutsch, Ivan; Jessen, Poul

    2016-05-01

    Squeezing of collective atomic spins is typically generated by quantum backaction from a QND measurement of the relevant spin component. In this scenario the degree of squeezing is determined by the measurement resolution relative to the quantum projection noise (QPN) of a spin coherent state (SCS). Greater squeezing can be achieved through optimization of the 3D geometry of probe and atom cloud, or by placing the atoms in an optical cavity. We explore here a complementary strategy that relies on quantum control of the large internal spin available in alkali atoms such as Cs. Using a combination of rf and uw magnetic fields, we coherently map the internal spins in our ensemble from the SCS (| f = 4, m = 4>) to a ``cat'' state which is an equal superposition of | f = 4, m = 4>and | f = 4, m = -4>. This increases QPN by a factor of 2 f = 8 relative to the SCS, and therefore the amount of backaction and spin-spin entanglement produced by our QND measurement. In a final step, squeezing generated in the cat state basis can be mapped back to the SCS basis, where it corresponds to increased squeezing of the physical spin. Our experiments suggest that up to 8dB of metrologically useful squeezing can be generated in this way, compared to ~ 3 dB in an otherwise identical experiment starting from a SCS.

  11. Nuclear techniques in food and agriculture 1990-2002. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications, including technical documents (TECDOCs), of the International Atomic Energy Agency issued between 1 January 1990 and 31 December 2002. It is divided into two parts. The first part lists all sales publications in alphabetical order by subject category whereas the second part lists all TECDOCs in alphabetical order by subject category. Most publications are issued in English, although some are also available in other languages

  12. Nuclear power, nuclear fuel cycle and waste management, 1986-1999. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with nuclear power and nuclear fuel cycle and waste management and issued during the period of 1986-1999. Some earlier titles which form part of an established series or are still considered of importance have been included. Most publications are in English. Proceedings of conferences, symposia and panels of experts may contain papers in languages other than English, but all of these papers have abstracts in English

  13. Agreement on the Privileges and Immunities of the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    The text of the Agreement on the Privileges and Immunities of the International Atomic Energy Agency, as approved by the Board of Governors on 1 July 1959, is re produced in this document for the information of all Members of the Agency. As required by section 38 of the Agreement, the Director General will transmit certified copies, in the Agency's four working languages, to the Government of each Member State

  14. Nuclear and radiological safety 1980-1994. International Atomic Energy Agency Publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with Nuclear and Radiological Safety issued during the period 1980-1994. The following aspects are covered: Uranium mining and milling, Fuel fabrication and storage, Nuclear power plants, Research reactors, Radiation sources and accelerators, Transport of radioactive materials, Waste repositories, Radiation protection, Accident response, Radioactive waste management, Safety analysis, Quality management, Legal and governmental aspects

  15. 6th International Workshop on Application of Lasers in Atomic Nuclei Research

    CERN Document Server

    Błaszczak, Z; Marinova, K; LASER 2004

    2006-01-01

    6th International Workshop on Application of Lasers in Atomic Nuclei Research, LASER 2004, held in Poznan, Poland, 24-27 May, 2004 Researchers and graduate students interested in the Mössbauer Effect and its applications will find this volume indispensable. The volume presents the most recent developments in the methodology of Mössbauer spectroscopy. Reprinted from Hyperfine Interactions (HYPE) Volume 162, 1-4

  16. Agreement on the Privileges and Immunities of the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    The Agreement on the Privileges and Immunities of the International Atomic Energy Agency, the text of which is reproduced herein, was approved by the Board of Governors on 1 July 1959. As required by section 38, the Director General has transmitted a certified copy of the Agreement to the Government of each Member of the Agency, and will transmit such a copy to the Government of every State that becomes a Member hereafter

  17. IAEA technical documents (TECDOCs) 1992-2002. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all technical documents (TECDOCs) of the International Atomic Energy Agency issued between 1 January 1992 and 31 December 2002. It is divided into two parts. The first part lists all documents in numerical order, starting with the most recent publication. The second part lists all documents by subject category, in alphabetical order within each category. Most publications are issued in English, although some are also available in other languages

  18. Amplitude internal friction peaks associated with the interaction between dislocation kinks and solute atoms in aluminium

    International Nuclear Information System (INIS)

    Early in 1950, Ke observed in slightly cold-worked dilute aluminium-copper solid solutions a pronounced low-frequency internal friction peak around room temperature as a function of strain amplitude in which the high-amplitude side of the peak decreases rapidly to a very small value. This paper reviews the experimental results since the work of Ke, with emphasis on cold-worked aluminium containing Cu or Mg as substitutional solute atoms. A dislocation kink dragging and break away model is suggested. The latest results show that this internal friction peak around room temperature consists of two separate peaks. The amplitude peak accompanying the lower temperature peak shifts toward lower amplitudes and that accompanying the higher temperature peak shifts toward higher amplitudes with an increase of temperature of measurement. The former amplitude peak appears at an amplitude range lower than that of the former peak. A mechanism of the double amplitude peaks is suggested in terms of the simultaneous occurrence of longitudinal core diffusion (LCD) and transverse core diffusion (TCD) of the solute atoms during the to and fro sidewise motion of the dislocation kinks. Some conclusions concerning the mechanism of Hasiguti peaks are drawn from the comparison with studies on the internal friction peaks associated with the interaction between dislocation kinks and solute atoms. (orig.)

  19. Migration behaviour of carbon atoms on clean diamond (0 0 1) surface: A first principle study

    Science.gov (United States)

    Liu, Xuejie; Xia, Qing; Li, Wenjuan; Luo, Hao; Ren, Yuan; Tan, Xin; Sun, Shiyang

    2016-01-01

    The adsorption and migration energies of a single carbon atom and the configuration evolution energies of two carbon atoms on a clean diamond (0 0 1) surface were calculated using the first principle method based on density functional theory to investigate the formation of ultra-nanocrystalline diamond (UNCD) film. The activation energy of a single atom diffusing along a dimer row is 1.96 eV, which is almost the same as that of a CH2 migrating along a dimer row under hydrogen-rich conditions. However, the activation energy of a single atom diffusing along a dimer chain is 2.66 eV, which is approximately 1.55 times greater than that of a CH2 migrating along a dimer chain in a hydrogen-rich environment. The configuration evolution of the two carbon atoms is almost impossible at common diamond film deposition temperatures (700-900 °C) because the activation energies reach 4.46 or 5.90 eV. Therefore, the high-energy barrier could result in insufficient migration of adatoms, leading to the formation of amorphous in UNCD films in hydrogen-poor CVD environment.

  20. Atomic scale observation of oxygen delivery during silver-oxygen nanoparticle catalysed oxidation of carbon nanotubes

    Science.gov (United States)

    Yue, Yonghai; Yuchi, Datong; Guan, Pengfei; Xu, Jia; Guo, Lin; Liu, Jingyue

    2016-07-01

    To probe the nature of metal-catalysed processes and to design better metal-based catalysts, atomic scale understanding of catalytic processes is highly desirable. Here we use aberration-corrected environmental transmission electron microscopy to investigate the atomic scale processes of silver-based nanoparticles, which catalyse the oxidation of multi-wall carbon nanotubes. A direct semi-quantitative estimate of the oxidized carbon atoms by silver-based nanoparticles is achieved. A mechanism similar to the Mars-van Krevelen process is invoked to explain the catalytic oxidation process. Theoretical calculations, together with the experimental data, suggest that the oxygen molecules dissociate on the surface of silver nanoparticles and diffuse through the silver nanoparticles to reach the silver/carbon interfaces and subsequently oxidize the carbon. The lattice distortion caused by oxygen concentration gradient within the silver nanoparticles provides the direct evidence for oxygen diffusion. Such direct observation of atomic scale dynamics provides an important general methodology for investigations of catalytic processes.

  1. Fragmentation of neutral carbon clusters formed by high velocity atomic collision

    International Nuclear Information System (INIS)

    The aim of this work is to understand the fragmentation of small neutral carbon clusters formed by high velocity atomic collision on atomic gas. In this experiment, the main way of deexcitation of neutral clusters formed by electron capture with ionic species is the fragmentation. To measure the channels of fragmentation, a new detection tool based on shape analysis of current pulse delivered by semiconductor detectors has been developed. For the first time, all branching ratios of neutral carbon clusters are measured in an unambiguous way for clusters size up to 10 atoms. The measurements have been compared to a statistical model in microcanonical ensemble (Microcanonical Metropolis Monte Carlo). In this model, various structural properties of carbon clusters are required. These data have been calculated with Density Functional Theory (DFT-B3LYP) to find the geometries of the clusters and then with Coupled Clusters (CCSD(T)) formalism to obtain dissociation energies and other quantities needed to compute fragmentation calculations. The experimental branching ratios have been compared to the fragmentation model which has allowed to find an energy distribution deposited in the collision. Finally, specific cluster effect has been found namely a large population of excited states. This behaviour is completely different of the atomic carbon case for which the electron capture in the ground states predominates. (author)

  2. Atomic carbon chains as spin-transmitters: An ab initio transport study

    DEFF Research Database (Denmark)

    Fürst, Joachim Alexander; Brandbyge, Mads; Jauho, Antti-Pekka

    2010-01-01

    An atomic carbon chain joining two graphene flakes was recently realized in a ground-breaking experiment by Jin et al. (Phys. Rev. Lett., 102 (2009) 205501). We present ab initio results for the electron transport properties of such chains and demonstrate complete spin-polarization of the transmi...

  3. The role of the atomic force function in molecular mechanics simulations for carbon nanostructures

    International Nuclear Information System (INIS)

    Molecular mechanics studies were performed on structures consisting of Y junctions of carbon nanotubes. Tensile simulations were run on the same structure, wherein atomic force functions of various shape were used. According to the numerical test results the behavior of the structure, the failure site and the failure process could be determined irrespective of the shape of the force function

  4. The Reception of J. H. van't Hoff's Theory of the Asymmetric Carbon Atom

    Science.gov (United States)

    Snelders, H. A. M.

    1974-01-01

    Discusses Jacobus Henricus van't Hoff's revolutionary theory of the asymmetric carbon atom and its early reception among his contemporaries in the Netherlands. Indicates that the extension of the new idea to practical problems gives the impetus to the development of stereochemistry. (CC)

  5. Electrocatalytic activity of atomic layer deposited Pt–Ru catalysts onto N-doped carbon nanotubes

    DEFF Research Database (Denmark)

    Johansson, Anne-Charlotte Elisabeth Birgitta; Larsen, Jackie Vincent; Verheijen, Marcel A.;

    2014-01-01

    Pt–Ru catalysts of various compositions, between 0 and 100at.% of Ru, were deposited onto N-doped multi-walled carbon nanotubes (N-CNTs) by atomic layer deposition (ALD) at 250°C. The Pt and Ru precursors were trimethyl(methylcyclopentadienyl)platinum (MeCpPtMe3) and bis...

  6. Reactions of the inner surface of carbon nanotubes and nanoprotrusion processes imaged at the atomic scale

    Science.gov (United States)

    Chamberlain, Thomas W.; Meyer, Jannik C.; Biskupek, Johannes; Leschner, Jens; Santana, Adriano; Besley, Nicholas A.; Bichoutskaia, Elena; Kaiser, Ute; Khlobystov, Andrei N.

    2011-09-01

    Although the outer surface of single-walled carbon nanotubes (atomically thin cylinders of carbon) can be involved in a wide range of chemical reactions, it is generally thought that the interior surface of nanotubes is unreactive. In this study, we show that in the presence of catalytically active atoms of rhenium inserted into nanotubes, the nanotube sidewall can be engaged in chemical reactions from the inside. Aberration-corrected high-resolution transmission electron microscopy operated at 80 keV allows visualization of the formation of nanometre-sized hollow protrusions on the nanotube sidewall at the atomic level in real time at ambient temperature. Our direct observations and theoretical modelling demonstrate that the nanoprotrusions are formed in three stages: (i) metal-assisted deformation and rupture of the nanotube sidewall, (ii) the fast formation of a metastable asymmetric nanoprotrusion with an open edge and (iii) a slow symmetrization process that leads to a stable closed nanoprotrusion.

  7. The effect of electrochemical phenomena on the deposition of carbon containing inorganic thin films from supersonic expansion of aqueous supercritical solutions

    Science.gov (United States)

    Sezer, Ali Osman

    The supersonic expansion of dilute aqueous solutions for the synthesis of new materials is a complex flow system. Flow prediction and modeling are, therefore, quite challenging. Electrokinetic streaming potentials generated during the supersonic nozzle expansion further complicate the nature of these flow processes. Flow-generated potentials are believed to significantly affect the electrochemical environment of the flow, and therefore, may influence the properties of the product. This dissertation research was an attempt to experimentally and theoretically investigate the significance of flow-generated electrochemical phenomena and their possible effect on the deposited thin carbon films. Brand's computer model was used to predict the physical properties of the expanding jet at the nozzle. The sensitivity of the predicted flow parameters to operating conditions was then analyzed. The results of this parametric flow modeling were used to identify deposition regions of flow space that have less sensitivity to fluctuations in process temperatures and pressures. Streaming currents were predicted from measured nozzle currents. The first high-temperature-pressure Pourbaix diagrams were constructed for the carbon-water system. Equilibrium Pourbaix diagrams together with predicted streaming currents suggested a possible CVD-like mechanism for the deposition of thin carbon films. Deposited carbon films were analyzed for morphology, composition and structure by vibrational spectroscopy and electron microscopy. IR and Raman analysis of carbon samples were not conclusive in revealing any measurable differences in samples. Although Raman spectra showed considerable shifts in peak positions, the lack of internal standard in the spectra made it difficult to draw any reliable conclusions. Significant variations in surface morphology were found for samples grown under different substrate bias. Electron diffraction analysis conclusively showed the presence of a cubic diamond and

  8. Multiphoton inner-shell ionization of the carbon atom

    CERN Document Server

    Rey, H F

    2015-01-01

    We apply time-dependent R-matrix theory to study inner-shell ionization of C atoms in ultra-short high-frequency light fields with a photon energy between 170 and 245 eV. At an intensity of 10$^{17}$ W/cm$^2$, ionization is dominated by single-photon emission of a $2\\ell$ electron, with two-photon emission of a 1s electron accounting for about 2-3\\% of all emission processes, and two-photon emission of $2\\ell$ contributing about 0.5-1\\%. Three-photon emission of a 1s electron is estimated to contribute about 0.01-0.03\\%. Around a photon energy of 225 eV, two-photon emission of a 1s electron, leaving C$^+$ in either 1s2s2p$^3$ or 1s2p$^4$ is resonantly enhanced by intermediate 1s2s$^2$2p$^3$ states. The results demonstrate the capability of time-dependent R-matrix theory to describe inner-shell ionization processes including rearrangement of the outer electrons.

  9. Adsorption of cadmium ions from aqueous solution using granular activated carbon and activated clay

    Energy Technology Data Exchange (ETDEWEB)

    Wasewar, Kailas L. [Department of Chemical Engineering, Visvesvaraya National Institute of Technology (VNIT), Nagpur, Maharashtra (India); Kumar, Pradeep; Teng, Tjoon Tow [Environmental Technology Division, School of Industrial Technology, University Science of Malaysia, Minden, Penang (Malaysia); Chand, Shri; Padmini, Bina N. [Department of Chemical Engineering, Indian Institute of Technology, Roorkee (India)

    2010-07-15

    The present study was aimed at removing cadmium ions from aqueous solution through batch studies using adsorbents, such as, granular activated carbon (GAC) and activated clay (A-clay). GAC was of commercial grade where as the A-clay was prepared by acid treatment of clay with 1 mol/L of H{sub 2}SO{sub 4}. Bulk densities of A-clay and GAC were 1132 and 599 kg/m{sup 3}, respectively. The surface areas were 358 m{sup 2}/g for GAC and 90 m{sup 2}/g for A-clay. The adsorption studies were carried out to optimize the process parameters, such as, pH, adsorbent dosage, and contact time. The results obtained were analyzed for kinetics and adsorption isotherm studies. The pH value was optimized at pH 6 giving maximum Cd removal of 84 and 75.2% with GAC and A-clay, respectively. The adsorbent dosage was optimized and was found to be 5 g/L for GAC and 10 g/L for A-clay. Batch adsorption studies were carried out with initial adsorbate (Cd) concentration of 100 mg/L and adsorbent dosage of 10 g/L at pH 6. The optimum contact time was found to be 5 h for both the adsorbents. Kinetic studies showed Cd removal a pseudo second order process. The isotherm studies revealed Langmuir isotherm to better fit the data than Freundlich isotherm. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  10. Adsorption of chlorophenols from aqueous solutions by pristine and surface functionalized single-walled carbon nanotubes.

    Science.gov (United States)

    Ding, Han; Li, Xin; Wang, Jun; Zhang, Xiaojian; Chen, Chao

    2016-05-01

    The adsorption of six kinds of chlorophenols on pristine, hydroxylated and carboxylated single-walled carbon nanotubes (SWCNTs) has been investigated. Pseudo-first order and pseudo-second order models were used to describe the kinetic data. All adsorption isotherms were well fitted with Langmuir, Freundlich and Polanyi-Manes models, due to surface adsorption dominating the adsorption process. The close linear relationship between logKow and logKd suggested that hydrophobicity played an important role in the adsorption. The SWCNTs' adsorption capacity for chlorophenols was weakened by addition of oxygen-containing functional groups on the surface, due to the loss of specific surface area, the increase of hydrophilicity and the reduction of π-π interaction. The best adsorption capacity of pristine SWCNTs, SWCNT-OH and SWCNT-COOH for six chlorophenols varied from 19 to 84mg/g, from 19 to 65mg/g and from 17 to 65mg/g, respectively. The effect of pH on the adsorption of 2,6-dichlorophenol (2,6-DCP), was also studied. When pH is over the pKa of 2,6-dichlorophenol (2,6-DCP), its removal dropped sharply. When ionic strength increased (NaCl or KCl concentration from 0 to 0.02mmol/L), the adsorption capacity of 2,6-DCP on pristine SWCNTs decreased slightly. The comparison of chlorophenols adsorption by SWCNTs, MWCNTs and PAC was made, indicating that the adsorption rate of CNTs was much faster than that of PAC. The results provide useful information about the feasibility of SWCNTs as an adsorbent to remove chlorophenols from aqueous solutions. PMID:27155424

  11. Multiwalled Carbon Nanotube/Cellulose Composite: From Aqueous Dispersions to Pickering Emulsions.

    Science.gov (United States)

    Avendano, Carlos; Brun, Nicolas; Fontaine, Olivier; In, Martin; Mehdi, Ahmad; Stocco, Antonio; Vioux, André

    2016-04-26

    A mild and simple way to prepare stable aqueous colloidal suspensions of composite particles made of a cellulosic material (Sigmacell cellulose) and multiwalled carbon nanotubes (MWCNTs) is reported. These suspensions can be dried and redispersed in water at pH 10.5. Starting with rather crude initial materials, commercial Sigmacell cellulose and MWCNTs, a significant fraction of composite dispersed in water could be obtained. The solid composites and their colloidal suspensions were characterized by electronic microscopy, thermal analyses, FTIR and Raman spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and light scattering. The composite particles consist of tenuous aggregates of CNTs and cellulose, several hundred nanometers large, and are composed of 55 wt % cellulose and 45 wt % CNTs. Such particles were shown to stabilize cyclohexane-in-water emulsions. The adsorption and the elasticity of the layer they form at interface were characterized by the pendant drop method. The stability of the oil-in-water emulsions was attributed to the formation of an elastic network of composite particles at interface. Cyclohexane droplet diameters could be tuned from 20 to 100 μm by adjusting the concentration of composite particles. This behavior was attributed to the limited coalescence phenomenon, just as expected for Pickering emulsions. Interestingly, cyclohexane droplets were stable over time and sustained pH modifications over a wide range, although acidic pH induced accelerated creaming. This study points out the possibility of combining crude cellulose and MWCNTs through a simple process to obtain colloidal systems of interest for the design of functional conductive materials. PMID:27052957

  12. Aqueous leaching of organic acids and dissolved organic carbon from various biochars prepared at different temperatures.

    Science.gov (United States)

    Liu, Peng; Ptacek, Carol J; Blowes, David W; Berti, William R; Landis, Richard C

    2015-03-01

    Biochar has been used as a soil amendment, as a water treatment material, and for carbon (C) sequestration. Thirty-six biochars, produced from wood, agricultural residue, and manure feedstocks at different temperatures, were evaluated for the aqueous leaching of different forms of soluble C. The release of inorganic C (alkalinity), organic acids (OAs), and total dissolved organic C (DOC) was highly variable and dependent on the feedstock and pyrolysis temperature. The pH and alkalinity increased for the majority of samples. Higher pH values were associated with high-temperature (high-T) (600 and 700°C) biochars. Statistically significant differences in alkalinity were not observed between low-temperature (low-T) (300°C) and high-T biochars, whereas alkalinity released from wood-based biochar was significantly lower than from others. Concentrations of OAs and DOC released from low-T biochars were greater than from high-T biochars. The C in the OAs represented 1 to 60% of the total DOC released, indicating the presence of other DOC forms. The C released as DOC represented up to 3% (majority biochar. Scanning electron microscopy with energy dispersive X-ray spectroscopy showed the high-T biochars had a greater proportion of micropores. Fourier transform infrared spectroscopy showed that hydroxyl, aliphatic, and quinone were the predominant functional groups of all biochars and that the abundance of other functional groups was dependent on the feedstock. The release of DOC, especially bioavailable forms such as OAs, may promote growth of organisms and heavy metal complexation and diminish the potential effectiveness of various biochars for C sequestration. PMID:26023986

  13. Internally consistent thermodynamic data for aqueous species in the system Na-K-Al-Si-O-H-Cl

    Science.gov (United States)

    Miron, George D.; Wagner, Thomas; Kulik, Dmitrii A.; Heinrich, Christoph A.

    2016-08-01

    A large amount of critically evaluated experimental data on mineral solubility, covering the entire Na-K-Al-Si-O-H-Cl system over wide ranges in temperature and pressure, was used to simultaneously refine the standard state Gibbs energies of aqueous ions and complexes in the framework of the revised Helgeson-Kirkham-Flowers equation of state. The thermodynamic properties of the solubility-controlling minerals were adopted from the internally consistent dataset of Holland and Powell (2002; Thermocalc dataset ds55). The global optimization of Gibbs energies of aqueous species, performed with the GEMSFITS code (Miron et al., 2015), was set up in such a way that the association equilibria for ion pairs and complexes, independently derived from conductance and potentiometric data, are always maintained. This was achieved by introducing reaction constraints into the parameter optimization that adjust Gibbs energies of complexes by their respective Gibbs energy effects of reaction, whenever the Gibbs energies of reactant species (ions) are changed. The optimized thermodynamic dataset is reported with confidence intervals for all parameters evaluated by Monte Carlo trial calculations. The new thermodynamic dataset is shown to reproduce all available fluid-mineral phase equilibria and mineral solubility data with good accuracy and precision over wide ranges in temperature (25-800 °C), pressure (1 bar to 5 kbar) and composition (salt concentrations up to 5 molal). The global data optimization process adopted in this study can be readily repeated any time when extensions to new chemical elements and species are needed, when new experimental data become available, or when a different aqueous activity model or equation of state should be used. This work serves as a proof of concept that our optimization strategy is feasible and successful in generating a thermodynamic dataset reproducing all fluid-mineral and aqueous speciation equilibria in the Na-K-Al-Si-O-H-Cl system within

  14. Energy use and carbon emissions: Some international comparisons

    International Nuclear Information System (INIS)

    This report examines international energy use patterns, trends, and energy-related carbon emissions since 1970. The main focus of this study is on the developed countries, represented by the members of the organization for Economic Cooperation and Development (OECD). The study is organized as follows: (1) the OECD is placed in a world context; (2) aggregate-level information is then presented for an important part of the OECD, namely the Group of Seven (G-7) major industrialized countries (the US, Canada, Japan, the United Kingdom, France, Italy, and Germany -- defined in this report as western Germany only, except where indicated); and (3) individual economic sectors within the G-7 countries are broken out for detailed review

  15. How molecular internal-geometric parameters affect PB-PEO polymersome size in aqueous solution

    DEFF Research Database (Denmark)

    Habel, Joachim Erich Otto; Ogbonna, Anayo; Larsen, Nanna; Schulte, Lars; Almdal, Kristoffer; Hélix-Nielsen, Claus

    2016-01-01

    Amphiphilic polybutadiene polyethylene oxide (PB-PEO) is one of the best known chemistries to form stable vesicular morphologies, stated as polymersomes, in aqueous environment. Mimicking cell membranes, these structures self-assemble in an “amphiphilic window” determined by 0.15 < f < 0.35 where f...... for subsequent tuning of size via extrusion. This can pave the way for cost-effective upscaling of polymersome production for biomedical and biomimetic applications. ©...

  16. International oil price’s impacts on carbon emission in China’s transportation industry

    OpenAIRE

    Guoxing Zhang; Sujie Cheng

    2014-01-01

    Purpose: This paper analyses the impact mechanism of international oil price on the industrial carbon emission, and uses the partial least squares regression model to study international oil price’s impact on carbon emissions in China’s transportation industry.Design/methodology/approach: This paper chooses five independent variables of GDP, international oil price, private car population, passenger and freight transportation volume as impact factors to investigate industrial carbon emissions...

  17. Analysis of Carbon Nanotubes on the Mechanical Properties at Atomic Scale

    Directory of Open Access Journals (Sweden)

    Xiaowen Lei

    2011-01-01

    Full Text Available This paper aims at developing a mathematic model to characterize the mechanical properties of single-walled carbon nanotubes (SWCNTs. The carbon-carbon (C–C bonds between two adjacent atoms are modeled as Euler beams. According to the relationship of Tersoff-Brenner force theory and potential energy acting on C–C bonds, material constants of beam element are determined at the atomic scale. Based on the elastic deformation energy and mechanical equilibrium of a unit in graphite sheet, simply form ED equations of calculating Young's modulus of armchair and zigzag graphite sheets are derived. Following with the geometrical relationship of SWCNTs in cylindrical coordinates and the structure mechanics approach, Young's modulus and Poisson's ratio of armchair and zigzag SWCNTs are also investigated. The results show that the approach to research mechanical properties of SWCNTs is a concise and valid method. We consider that it will be useful technique to progress on this type of investigation.

  18. Evaluating carbon dioxide emissions in international trade of China

    International Nuclear Information System (INIS)

    China is the world's largest emitter of carbon dioxide (CO2). As exports account for about one-third of China's GDP, the CO2 emissions are related to not only China's own consumption but also external demand. Using the input-output analysis (IOA), we analyze the embodied CO2 emissions of China's import and export. Our results show that about 3357 million tons CO2 emissions were embodied in the exports and the emissions avoided by imports (EAI) were 2333 million tons in 2005. The average contribution to embodied emission factors by electricity generation was over 35%. And that by cement production was about 20%. It implies that the production-based emissions of China are more than the consumption-based emissions, which is evidence that carbon leakage occurs under the current climate policies and international trade rules. In addition to the call for a new global framework to allocate emission responsibilities, China should make great efforts to improve its energy efficiency, carry out electricity pricing reforms and increase renewable energy. In particular, to use advanced technology in cement production will be helpful to China's CO2 abatement. (author)

  19. Corrosion inhibition behavior of propyl phosphonic acid–Zn2+ system for carbon steel in aqueous solution

    International Nuclear Information System (INIS)

    The effectiveness of propyl phosphonic acid (PPA) as a corrosion inhibitor in association with a bivalent cation like Zn2+ has been studied. An eco-friendly inhibitor in controlling corrosion of carbon steel in neutral aqueous medium in the absence and presence of Zn2+ has been evaluated by gravimetric method. Impedance studies of the metal/solution interface indicated that the surface film is highly protective against the corrosion of carbon steel in the aqueous environment. Potentiodynamic polarization studies showed that the inhibitor is a mixed inhibitor. X-ray photoelectron spectroscopic analysis (XPS) of the protective film exhibited the presence of the elements viz., iron, phosphorus, oxygen, carbon and zinc. The chemical shifts in the binding energies of these elements inferred that the surface film is composed of oxides/hydroxides of iron(III), Zn(OH)2 and [Fe(II)/(III)–Zn(II)–PPA] complex. Further, the surface analysis techniques viz., FT-IR, AFM and SEM studies confirm the formation of an adsorbed protective film on the carbon steel surface. Based on all these results, a plausible mechanism of corrosion inhibition is proposed.

  20. IUPAC-NIST Solubility Data Series. 95. Alkaline Earth Carbonates in Aqueous Systems. Part 1. Introduction, Be and Mg

    Science.gov (United States)

    De Visscher, Alex; Vanderdeelen, Jan; Königsberger, Erich; Churagulov, Bulat R.; Ichikuni, Masami; Tsurumi, Makoto

    2012-03-01

    The alkaline earth carbonates are an important class of minerals. This volume compiles and critically evaluates solubility data of the alkaline earth carbonates in water and in simple aqueous electrolyte solutions. Part 1, the present paper, outlines the procedure adopted in this volume in detail, and presents the beryllium and magnesium carbonates. For the minerals magnesite (MgCO3), nesquehonite (MgCO3.3H2O), and lansfordite (MgCO3.5H2O), a critical evaluation is presented based on curve fits to empirical and/or thermodynamic models. Useful side products of the compilation and evaluation of the data outlined in the introduction are new relationships for the Henry constant of CO2 with Sechenov parameters, and for various equilibria in the aqueous phase including the dissociation constants of CO2(aq) and the stability constant of the ion pair MCO30(aq) (M = alkaline earth metal). Thermodynamic data of the alkaline earth carbonates consistent with two thermodynamic model variants are proposed. The model variant that describes the Mg2+-HCO3- ion interaction with Pitzer parameters was more consistent with the solubility data and with other thermodynamic data than the model variant that described the interaction with a stability constant.

  1. Internal corrosion of carbon steel piping in hot aquifers service

    Directory of Open Access Journals (Sweden)

    Simičić Miloš V.

    2011-01-01

    Full Text Available Internal corrosion of carbon steel pipelines is a major problem encountered in water service. In terms of prediction of the remaining lifetime for water pipelines based on the corrosion allowance, the three main approaches are corrosion modelling, corrosion inhibitor availability, and corrosion monitoring. In this study we used two theoretical corrosion models, CASSANDRA and NORSOK M-506 of quite different origin in order to predict uniform corrosivity of hot aquifers in eight different pipelines. Because of the varying calculation criteria for the different models, these can give very different corrosion rate predictions for the same data input. This is especially true under conditions where the formation of protective films may occur, such as at elevated temperatures. The evaluation of models was conducted by comparison using weight-loss coupons and three corrosion inhibitors were obtained from commercial suppliers. The tests were performed during the 60-day period. Even though inhibitors’ efficiencies of 98% had been achieved in laboratory testing, inhibitors’ availabilities of 85% have been used due to logistics problems and other issues. The results, given in mmpy, i.e. millimeter per year, are very consistent with NORSOK M-506 prediction. This is presumably because the model considers the effect of the formation of a passive iron carbonate film at temperatures above 80 °C and significant reduction in corrosion rate. Corrosion inhibitor A showed a better performance than inhibitors B and C in all cases but the target corrosion rates of less than 0.1 mmpy were achieved for all inhibitors. The chemical type of corrosion inhibitor A is based on quaternary amines mixed with methanol, isopropyl alcohol, xylene and ethylbenzene. Based on the obtained results the carbon steel lifetime of 30 years, provided proper inhibitors are present and 3mm corrosion allowance, can be achieved for hot aquifers service with presented water compositions.

  2. Monte Carlo Technique Used to Model the Degradation of Internal Spacecraft Surfaces by Atomic Oxygen

    Science.gov (United States)

    Banks, Bruce A.; Miller, Sharon K.

    2004-01-01

    Atomic oxygen is one of the predominant constituents of Earth's upper atmosphere. It is created by the photodissociation of molecular oxygen (O2) into single O atoms by ultraviolet radiation. It is chemically very reactive because a single O atom readily combines with another O atom or with other atoms or molecules that can form a stable oxide. The effects of atomic oxygen on the external surfaces of spacecraft in low Earth orbit can have dire consequences for spacecraft life, and this is a well-known and much studied problem. Much less information is known about the effects of atomic oxygen on the internal surfaces of spacecraft. This degradation can occur when openings in components of the spacecraft exterior exist that allow the entry of atomic oxygen into regions that may not have direct atomic oxygen attack but rather scattered attack. Openings can exist because of spacecraft venting, microwave cavities, and apertures for Earth viewing, Sun sensors, or star trackers. The effects of atomic oxygen erosion of polymers interior to an aperture on a spacecraft were simulated at the NASA Glenn Research Center by using Monte Carlo computational techniques. A two-dimensional model was used to provide quantitative indications of the attenuation of atomic oxygen flux as a function of the distance into a parallel-walled cavity. The model allows the atomic oxygen arrival direction, the Maxwell Boltzman temperature, and the ram energy to be varied along with the interaction parameters of the degree of recombination upon impact with polymer or nonreactive surfaces, the initial reaction probability, the reaction probability dependence upon energy and angle of attack, degree of specularity of scattering of reactive and nonreactive surfaces, and the degree of thermal accommodation upon impact with reactive and non-reactive surfaces to be varied to allow the model to produce atomic oxygen erosion geometries that replicate actual experimental results from space. The degree of

  3. Preparation and characterization of carbon supported nano-nickel and its sorption behavior for zinc from aqueous solutions

    International Nuclear Information System (INIS)

    Nickel deposited on carbon has been used as adsorbent to recover Zn (II) from aqueous system. The adsorbent was synthesized by depositing nickel nitrate on carbon under inert conditions and decomposing it to nickel by raising the temperature, washing and vacuum drying. Various techniques including XRD, FTIR, and SEM were employed for its characterization. FTIR showed that the nickel deposition enhanced the carbon functionalization due to presence of OH, C=O and C-O groups. Average crystallite size of about 9 nm was determined from XRD. Nickel deposition resulted in further division particles as indicated from the morphological study. Zn (II) was subjected to adsorption on the synthesized adsorbent. It was observed that the rate of adsorption increased significantly on the nickel deposited carbon than the carbon alone. Morris-Weber, Lagrangian and Reichenberg models were applied to find out the type and rate of adsorption employing first and second order rate equations. The adsorption data were applied to Langmuir, Freundlich and D-R isotherms and values of isotherm constants were calculated and were higher for Ni/C than carbon alone. The mean free energy of zinc sorption on carbon and Ni/C are 16.67 and 18.26 kJmol/sup -1/ which shows chemisorption. Thermodynamic studies were done to find out the effect of temperature on sorption. Positive values of del H and negative values of del G show endothermic and spontaneous type of sorption. (author)

  4. Modeling the Mechanical Properties of Functionalized Carbon Nanotubes and Their Composites: Design at the Atomic Level

    Directory of Open Access Journals (Sweden)

    Qing-Sheng Yang

    2014-01-01

    Full Text Available This investigation focuses on the design of functionalization configuration at the atomic level to determine the influence of atomic structure on the mechanical properties of functionalized carbon nanotubes (F-CNTs and their composites. Tension and compressive buckling behaviors of different configurations of CNTs functionalized by H atoms are studied by a molecular dynamics (MD method. It is shown that H-atom functionalization reduces Young’s modulus of CNTs, but Young’s modulus is not sensitive to the functionalization configuration. The configuration does, however, affect the tensile strength and critical buckling stress of CNTs. Further, the stress-strain relations of composites reinforced by nonfunctionalized and various functionalized CNTs are analyzed.

  5. Low-temperature carbon monoxide oxidation catalysed by regenerable atomically dispersed palladium on alumina

    Science.gov (United States)

    Peterson, Eric J.; Delariva, Andrew T.; Lin, Sen; Johnson, Ryan S.; Guo, Hua; Miller, Jeffrey T.; Hun Kwak, Ja; Peden, Charles H. F.; Kiefer, Boris; Allard, Lawrence F.; Ribeiro, Fabio H.; Datye, Abhaya K.

    2014-09-01

    Catalysis by single isolated atoms of precious metals has attracted much recent interest, as it promises the ultimate in atom efficiency. Most previous reports are on reducible oxide supports. Here we show that isolated palladium atoms can be catalytically active on industrially relevant γ-alumina supports. The addition of lanthanum oxide to the alumina, long known for its ability to improve alumina stability, is found to also help in the stabilization of isolated palladium atoms. Aberration-corrected scanning transmission electron microscopy and operando X-ray absorption spectroscopy confirm the presence of intermingled palladium and lanthanum on the γ-alumina surface. Carbon monoxide oxidation reactivity measurements show onset of catalytic activity at 40 °C. The catalyst activity can be regenerated by oxidation at 700 °C in air. The high-temperature stability and regenerability of these ionic palladium species make this catalyst system of potential interest for low-temperature exhaust treatment catalysts.

  6. Supercritical carbon dioxide extractions of agricultural chemicals from aqueous solutions; Chorinkai nisankatanso ni yoru suiyoeki karano noyaku no chushitsu

    Energy Technology Data Exchange (ETDEWEB)

    Nakai, T.; Sato, Y.; Takahashi, N.; Kato, Y. [National Inst. for Resources and Environment, Tsukuba (Japan). Advanced Water Treatment Division

    1999-12-10

    Examination was made on the supercritical carbon dioxide extraction of agricultural chemicals from aqueous solutions. In the case of the semi batch extraction blowing supercritical carbon dioxide into the aqueous solutions at a concentration of 5 mg L{sup -1}, the dependencies of the removal ratios of four kinds of agricultural chemicals on temperature and pressure were shown in different patterns depending on the agricultural chemicals. For simazin (CAT), no unusual phenomena were observed. On the other hand, isoprothiolane (IPT) exhibited unusual phenomena. That is, the removal ratios decreased, as the pressure increased above 100 kg cm{sup -2} at temperatures of 45 degree C and 50 degree C. A similar phenomenon was observed for fenitrothion (MEP) or napropamide (NPP). Complicate pattern was shown for MEP. The removal ratios at pressures of 80 kg cm{sup -2} and 90 kg cm{sup -2} had maxima at 40 degree C and 45 degree C, respectively. These phenomena were discussed in terms of equilibrium and mass transfer. It was referred to that consideration should be given to such phenomena when the extraction technique is used for analysis. The order of the easiness of the separation of agricultural chemical from aqueous solution (that was estimated by the removal ratio at temperature of 35 degree C and pressure of 100 kg cm{sup -2}) was IPT>NPP>MEP>CAT. Correlation was seen between the removal ratio and the solubility of agricultural chemical in water, and in hexane or the melting point. (author)

  7. Hybrid capacitors utilizing halogen-based redox reactions at interface between carbon positive electrode and aqueous electrolytes

    Science.gov (United States)

    Yamazaki, Shigeaki; Ito, Tatsuya; Murakumo, Yuka; Naitou, Masashi; Shimooka, Toshiharu; Yamagata, Masaki; Ishikawa, Masashi

    2016-09-01

    We propose novel hybrid capacitors (HCs) with electrolyte-involved redox reactions of bromide or iodide species by pretreatment of an activated carbon positive electrode. The treatment is simple; impregnation of pores at an activated carbon fiber cloth (ACFC) as a positive electrode with bromine- or iodine-containing water before cell assembly. The treated positive electrode is applied to a HC cell with a non-treated negative electrode of ACFC and its electrochemical performance is investigated by galvanostatic cycling and leakage current tests. Few studies on such "electrolytic" charge storage systems have provided acceptable capacitor performance because of inevitable self-discharge caused by diffusion of charged species form an electrode to the other one through an electrolyte. Nevertheless, our electrolyte-redox-based HCs show excellent performance without undesirable diffusion of charged species. Moreover, the present HC utilizing a bromide redox system fulfills a practical cell voltage of 1.8 V in spite of an aqueous electrolyte system. This high voltage provides excellent energy density, which is 5 times higher than that in a conventional aqueous electric double-layer capacitor (EDLC), and 1.2 times higher even than that in a 2.7 V-class non-aqueous EDLC, while keeping high charge-discharge rate capability.

  8. Energetic changes in the surface of activated carbons and relationship with Ni(II) adsorption from aqueous solution

    Science.gov (United States)

    Rodríguez-Estupiñan, Paola; Giraldo, Liliana; Moreno-Piraján, Juan Carlos

    2013-12-01

    This study investigated Ni(II) ion adsorption from aqueous solution on activated carbons obtained by chemically modifying the surface with the oxidizing agents nitric acid and hydrogen peroxide (CAGoxP and CAGoxN, respectively). The activated carbons were characterized by total acidity and basicity, pH at the point of charge zero determination and IR spectroscopy. Textural parameters such as the BET area and pore volumes were evaluated by gas adsorption. The BET area of the materials was between 816 and 876 m2 g-1. Additionally, the immersion enthalpies of the activated carbons in water and benzene were determined. The experimental results on adsorption in solution were adjusted to the Langmuir and Freundlich models, obtaining values for the monolayer capacity between 29.68 and 50.97 mg g-1, which indicates that the adsorption capacity depends largely on solid surface chemistry.

  9. Polymorph selection and nanocrystallite rearrangement of calcium carbonate in carboxymethyl chitosan aqueous solution: Thermodynamic and kinetic analysis

    International Nuclear Information System (INIS)

    In this article, the polymorph selection of calcium carbonate has been successfully achieved in water-soluble carboxymethyl chitosan aqueous solution at different temperatures (25-95 oC). Vaterite is formed in carboxymethyl chitosan solution 25 oC accompanied with trace of calcite, whereas pure aragonite is obtained at 95 oC. Scanning electron microscopy and transmission electron microscopy analyses show that the products are formed from the recrystallization of nanometer crystallites. Thermodynamic and kinetic analyses reveal that the polymorph of calcium carbonate is controlled and selected by kinetics in various temperatures. As a heterogeneous nucleator and stabilizing agent, carboxymethyl chitosan changes the nucleation and growth of calcium carbonate from thermodynamic into kinetic control. Under kinetic limitation, the reaction rate of aragonite increases along with the elevating of temperature and surpasses the rate of vaterite above 327 K.

  10. Polymorph selection and nanocrystallite rearrangement of calcium carbonate in carboxymethyl chitosan aqueous solution: Thermodynamic and kinetic analysis

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Donghui [Key Lab For Special Functional Materials Ministry of Education, Henan University, Kaifeng 475004 (China); Key Lab of Inorganic Coating Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi, Changning, Shanghai 200050 (China); Zhu, Yingchun, E-mail: yzhu@mail.sic.ac.cn [Key Lab of Inorganic Coating Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi, Changning, Shanghai 200050 (China); Li, Fang; Ruan, Qichao [Key Lab of Inorganic Coating Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi, Changning, Shanghai 200050 (China); Zhang, Shengmao [Key Lab For Special Functional Materials Ministry of Education, Henan University, Kaifeng 475004 (China); Zhang, Linlin; Xu, Fangfang [Key Lab of Inorganic Coating Materials, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi, Changning, Shanghai 200050 (China)

    2010-01-15

    In this article, the polymorph selection of calcium carbonate has been successfully achieved in water-soluble carboxymethyl chitosan aqueous solution at different temperatures (25-95 {sup o}C). Vaterite is formed in carboxymethyl chitosan solution 25 {sup o}C accompanied with trace of calcite, whereas pure aragonite is obtained at 95 {sup o}C. Scanning electron microscopy and transmission electron microscopy analyses show that the products are formed from the recrystallization of nanometer crystallites. Thermodynamic and kinetic analyses reveal that the polymorph of calcium carbonate is controlled and selected by kinetics in various temperatures. As a heterogeneous nucleator and stabilizing agent, carboxymethyl chitosan changes the nucleation and growth of calcium carbonate from thermodynamic into kinetic control. Under kinetic limitation, the reaction rate of aragonite increases along with the elevating of temperature and surpasses the rate of vaterite above 327 K.

  11. Adsorption of Cd(II and Pb(II Ions from Aqueous Solution byActivated Carbon

    Directory of Open Access Journals (Sweden)

    Hayder Mohammed Abdul-Hameed

    2009-01-01

    Full Text Available Heavy metal consider as major environmental pollutants. Many of industrial wastewater effluents contain a wide range of these heavy metals. The adsorption of Cd2+ and Pb2+ metal ions from aqueous solution by activated carbon was studied. The results showed that maximum adsorption capacity occurred at 486.9×10-3 mg/kg for Pb2+ ion and 548.8×10-3 mg/kg for Cd2+ ion. The adsorption in a mixture of the metal ions had a balancing effect on the adsorption capacity of the activated carbon. The adsorption capacity of each metal ion was affected by the presence of other metal ions rather than its presence individually. The study showed the presence of other heavy metals attribute to the reduction in the activated carbon capacity, and the adsorption process was found to obeys the Freundlich isotherm for both ions.

  12. Preparation and characterization of porous carbon from expanded graphite for high energy density supercapacitor in aqueous electrolyte

    Science.gov (United States)

    Barzegar, Farshad; Bello, Abdulhakeem; Momodu, Damilola; Madito, Moshawe Jack; Dangbegnon, Julien; Manyala, Ncholu

    2016-03-01

    In this work, we present the synthesis of low cost carbon nanosheets derived from expanded graphite dispersed in Polyvinylpyrrolidone, subsequently activated in KOH and finally carbonized in Ar/H2 atmosphere. Interconnected sheet-like structure with low concentration of oxygen (9.0 at.%) and a specific surface area of 457 m2 g-1 was obtained. The electrochemical characterization of the carbon material as supercapacitor electrode in a 2-electrode configuration shows high specific capacitance of 337 F g-1 at a current density of 0.5 A g-1 as well as high energy density of 37.9 Wh kg-1 at a power density of 450 W kg-1. This electrical double layer capacitor electrode also exhibits excellent stability after floating test for 120 h in 6 M KOH aqueous electrolyte. These results suggest that this activated expanded graphite (AEG) material has great potential for high performance electrode in energy storage applications.

  13. Functionalization of terminal carbon atoms of hydroxyl terminated polybutadiene by polyazido nitrogen rich molecules

    Indian Academy of Sciences (India)

    Rajavelu Murali Sankar; Tapta Kanchan Roy; Tushar Jana

    2011-07-01

    We report a novel synthetic approach for the attachment of the polyazido nitrogen rich molecule on to the hydroxyl terminated polybutadiene (HTPB) backbone. The terminal carbon atoms of the HTPB are functionalized by attaching cyanuric chloride (CYC) covalently on the HTPB backbone. Further reaction of this modified HTPB with sodium azide yields polyazido nitrogen rich HTPB. The unique physico-chemical properties and the microstructure of the HTPB do not get affected upon modification. IR, gel permeable chromatography (GPC) and absorption spectroscopy studies prove that the polyazido nitrogen rich molecules are covalently attached at the terminal carbon atoms of the HTPB. The π electron delocalization owing to long butadiene chain, strong electron withdrawing effect of the triazine molecules are the major driving forces for the covalent attachment of the triazine at the terminal carbon atoms of the HTPB. The disruption of the intermolecular hydrogen bonding between the terminal hydroxyl groups of the HTPB chains and the presence of hydrogen bonding between the N atoms of the triazine ring with OH group of the HTPB are observed. Theoretical study also reveals the existence of the hydrogen bonding between the OH and N. Theoretical calculation shows that the detonation performance of the polyazido nitrogen rich HTPB are very promising.

  14. Defect effect on tribological behavior of diamond-like carbon films deposited with hydrogen diluted benzene gas in aqueous environment

    Science.gov (United States)

    Yi, Jin Woo; Park, Se Jun; Moon, Myoung-Woon; Lee, Kwang-Ryeol; Kim, Seock-Sam

    2009-05-01

    This study examined the friction and wear behavior of diamond-like carbon (DLC) films deposited from a radio frequency glow discharge using a hydrogen diluted benzene gas mixture. The DLC films were deposited on Si (1 0 0) and polished stainless steel substrates by radio frequency plasma-assisted chemical vapor deposition (r.f.-PACVD) at hydrogen to benzene ratios, or the hydrogen dilution ratio, ranging from 0 to 2.0. The wear test was carried out in both ambient and aqueous environments using a homemade ball-on-disk type wear rig. The stability of the DLC coating in an aqueous environment was improved by diluting the benzene precursor gas with hydrogen, suggesting that hydrogen dilution during the deposition of DLC films suppressed the initiation of defects in the film and improved the adhesion of the coating to the interface.

  15. Effective removal of tetracycline from aqueous solution using activated carbon prepared from tomato (Lycopersicon esculentum Mill.) industrial processing waste.

    Science.gov (United States)

    Sayğılı, Hasan; Güzel, Fuat

    2016-09-01

    Activated carbon (TAC) prepared under optimized conditions with ZnCl2 activation from a new precursor; tomato industrial processing waste (TW), was applied as an adsorbent to remove tetracycline (TC) from aqueous solution. The factors (TAC dosage, initial TC concentration, contact time, ionic strength and solution temperature) affecting the adsorption process were examined at natural pH (5.7) of TAC-TC system in aqueous solution. Kinetic data was found to be best complied by the pseudo-second order model. The isotherm analysis indicated that the equilibrium data could be represented by the Langmuir model. The maximum adsorption capacity was identified as 500.0mgg(-1) at 308K. PMID:27177317

  16. International bulletin on atomic and molecular data for fusion. No. 66, August 2007

    International Nuclear Information System (INIS)

    Information in this Bulletin is presented in four parts. The Atomic and Molecular Data Information System (AMDIS) of the International Atomic Energy Agency is presented in Part 1. The indexed papers are listed separately for structure and spectra, atomic and molecular collisions, and surface interactions in Part 2. The structure and spectra indexation lines are grouped by process. The first column gives the process, the second one the reactants and then the character of the data contained (Th for theoretical, Ex for experimental, and E/T for both experimental and theoretical). The number in the last column is the reference number in Part 3 of the Bulletin. The atomic and molecular indexation lines are grouped by one collision partner (photon, electron or heavy particle). The first column gives the reactants, the second column gives the process, the third column gives the energy range with the appropriate units, and the last two columns are the same as in the structure and spectra indexation lines. The particle-surface interactions indexation lines are grouped by process. The first column gives the reactants, the second the energy range with the appropriate units, and the last two columns are the same as in the previous cases. Part 3 contains all the bibliographic data for both the indexed and non-indexed references. Those references which are indexed in Part 1 are identified by the repeated indexation lines. The Author Index (Part 4) refers to the bibliographic references contained in Part 3

  17. International bulletin on atomic and molecular data for fusion. No. 68, December 2009

    International Nuclear Information System (INIS)

    Information in this Bulletin is presented in four parts. The Atomic and Molecular Data Information System (AMDIS) of the International Atomic Energy Agency is presented in Part 1. The indexed papers are listed separately for structure and spectra, atomic and molecular collisions, and surface interactions in Part 2. The structure and spectra index lines are grouped by process. The first column gives the reactants, the second one the process and then the character of the data contained (Th for theoretical, Ex for experimental, and E/T for both experimental and theoretical). The number in the last column is the reference number in Part 3 of the Bulletin. The atomic and molecular index lines are grouped by one collision partner (photon, electron or heavy particle). The first column gives the reactants, the second column gives the process, the third column gives the energy range with the appropriate units, and the last two columns are the same as in the structure and spectra index lines. The particle-surface interactions index lines are grouped by process. The first column gives the reactants, the second the energy range with the appropriate units, and the last two columns are the same as in the previous cases. Part 3 contains all the bibliographic data for both the indexed and non-indexed references. Those references which are indexed in Part 1 are identified by the repeated index lines. The Author Index (Part 4) refers to the bibliographic references contained in Part 3

  18. Activated carbons from potato peels: The role of activation agent and carbonization temperature of biomass on their use as sorbents for bisphenol A uptake from aqueous solutions

    Science.gov (United States)

    Arampatzidou, An; Deliyanni, Eleni A.

    2015-04-01

    Activated carbons prepared from potato peels, a solid waste by product, and activated with different activating chemicals, have been studied for the adsorption of an endocrine disruptor (Bisphenol-A) from aqueous solutions. The potato peels biomass was activated with phosphoric acid, KOH and ZnCl2. The different activating chemicals were tested in order the better activation agent to be found. The carbons were carbonized by pyrolysis, in one step procedure, at three different temperatures in order the role of the temperature of carbonization to be pointed out. The porous texture and the surface chemistry of the prepared activated carbons were characterized by Nitrogen adsorption (BET), Scanning Electron Microscope (SEM), thermal analysis (DTA) and Fourier Transform Infrared Spectroscopy (FTIR). Batch experiments were performed to investigate the effect of pH, the adsorbent dose, the initial bisphenol A concentration and temperature. Equilibrium adsorption data were analyzed by Langmuir and Freundlich isotherms. The thermodynamic parameters such as the change of enthalpy (ΔH0), entropy (ΔS0) and Gibb's free energy (ΔG0) of adsorption systems were also evaluated. The adsorption capacity calculated from the Langmuir isotherm was found to be 450 mg g-1 at an initial pH 3 at 25 °C for the phosphoric acid activated carbon, that make the activated carbon a promising adsorbent material.

  19. 6. international conference on Nano-technology in Carbon: from synthesis to applications of nano-structured carbon and related materials

    International Nuclear Information System (INIS)

    This is the sixth international conference sponsored this year by the French Carbon Group (GFEC), the European Research Group on Nano-tubes GDRE 'Nano-E', in collaboration with the British Carbon Group and the 'Institut des Materiaux Jean Rouxel' (local organizer). The aim of this conference is to promote carbon science in the nano-scale as, for example, nano-structured carbons, nano-tubes, nano-wires, fullerenes, etc. This conference is designed to introduce those with an interest in materials to current research in nano-technology and to bring together research scientists working in various disciplines in the broad area of nano-structured carbons, nano-tubes and fullerene-related nano-structures. Elemental carbon is the simplest exemplar of this nano-technology based on covalent bonding, however other systems (for example containing hetero-atoms) are becoming important from a research point of view, and provide alternative nano-materials with unique properties opening a broad field of applications. Nano-technology requires an understanding of these materials on a structural and textural point of view and this will be the central theme. This year the conference will feature sessions on: S1. Control and synthesis of nano-materials 1.1 Nano-structured carbons: pyrolysis of polymers, activation, templates,... 1.2 Nano-tubes: Catalytic method, HiPCO, graphite vaporization, electrolysis,... 1.3 Fullerenes S2. Chemistry of carbon nano-materials 2.1 Purification of carbon nano-tubes 2.2 Functionalization - Self-assembling S3. Structural characterization S4. Theory and modelling S5. Relationship between structure and properties S6. Applications Water and air purification, Gas and energy storage, Composite materials, Field emission, Nano-electronics, Biotechnology,... S7. Environmental impact. Only one paper concerning carbon under irradiation has been added to the INIS database. (authors)

  20. Separation of Co2+ present in aqueous solution on calcium carbonate

    International Nuclear Information System (INIS)

    The CaCO3 was synthesized by precipitation method and characterized using SEM, EDS, TGA and IR. It was studied the adsorption behavior of Co2+ present in aqueous solution on the synthesized material by experiments batch type at room temperature. Was found that removal of cobalt ions was greater than 40% indicating that this material can be used to remove Co2+ present in aqueous solution. (Author)

  1. Hope over fear. The establishment of the International Atomic Energy Agency

    Energy Technology Data Exchange (ETDEWEB)

    Forland, A.

    1995-12-01

    President Eisenhower`s ``Atoms for Peace`` speech in 1953 started a process that led to the establishment of the International Atomic Energy Agency (IAEA). This study analyses the negotiations of the Statute of the Agency. It focuses on how the Agency`s scope of action regarding safeguards was negotiated. The Statute is seen as a reflection of the dual purpose of the new Agency to promote peaceful uses of nuclear energy, and to control that peaceful nuclear activities receiving IAEA assistance are not diverted to military purposes. On one hand, the countries receiving assistance from the Agency accepted a degree of international control that represented a breakthrough in international relations. On the other hand, many countries strongly resented controls. Consequently, compromises had to be made in the course of the negotiations in order to reach a consensus. Thus, although the IAEA was established as a competent and technical body, the underlying compromises meant that its scope of actions was restricted. 6 refs.

  2. Topography and Mechanical Property Mapping of International Simple Glass Surfaces with Atomic Force Microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Pierce, Eric M [ORNL

    2014-01-01

    Quantitative Nanomechanical Peak Force (PF-QNM) TappingModeTM atomic force microscopy measurements are presented for the first time on polished glass surfaces. The PF-QNM technique allows for topography and mechanical property information to be measured simultaneously at each pixel. Results for the international simple glass which represents a simplified version of SON68 glass suggests an average Young s modulus of 78.8 15.1 GPa is within the experimental error of the modulus measured for SON68 glass (83.6 2 GPa) with conventional approaches. Application of the PF-QNM technique will be extended to in situ glass corrosion experiments with the goal of gaining atomic-scale insights into altered layer development by exploiting the mechanical property differences that exist between silica gel (e.g., altered layer) and pristine glass surface.

  3. Synthesis and utilization of a novel carbon nanotubes supported nanocables for the adsorption of dyes from aqueous solutions

    Science.gov (United States)

    Liu, Wei; Jiang, Xinyu; Chen, Xiaoqing

    2015-09-01

    Using multiwalled carbon nanotubes(MWCNTs) as mechanical support and glucose as carbon resource, a hydrothermal carbonization route was designed for the synthesis of MWCNTs@carbon nanocables with tunable diameter and length. MWCNTs are firstly used as templates for the formation of carbon-rich composite nanocables, and the diameter of the nanocables could be tailored through adjusting the hydrothermal time or the ratio of MWCNTs and glucose. Owing to abundant superficial oxygen-containing functional groups, porous surface and remarkable reactivity, the as-synthesized nanocables are capable of efficiently adsorbing cationic dye methylene blue (MB) and crystal violet (CV). Furthermore, the optimum adsorption conditions, kinetics, adsorption isotherms and adsorption thermodynamics of dyes were studied systematically. Additionally, the maximum adsorption capacities calculated from data analysis (298.5 mg/g for MB and 228.3 mg/g for CV) are significant higher than those of raw MWCNTs and some other adsorbents reported previously, which provides strong evidence for using MWCNTs@carbon nanocables as adsorbent to remove dyes from aqueous solutions.

  4. Conductance of a single-atom carbon chain with graphene leads

    OpenAIRE

    Chen, Wei; Andreev, A. V.; Bertsch, G. F.

    2008-01-01

    We study the conductance of an interconnect between two graphene leads formed by a single-atom carbon chain. Its dependence on the chemical potential and the number of atoms in the chain is qualitatively different from that in the case of normal metal leads. Electron transport proceeds via narrow resonant states in the wire. The latter arise due to strong reflection at the junctions between the chain and the leads, which is caused by the small density of states in the leads at low energy. The...

  5. Communication of 31 March 1995 received from the Permanent Mission of South Africa to the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    The Secretariat of the International Atomic Energy Agency has received a note verbale of 31 March 1995 from the Permanent Mission of South Africa providing information on the nuclear export policies and practices of the Government of South Africa

  6. Communication of 23 March 1995 received from the Permanent Mission of Ukraine to the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    The Secretariat of the International Atomic Energy Agency has received a note verbale of 23 March 1995 from the Permanent Mission of Ukraine providing information on the nuclear export policies and practices of the Government of Ukraine

  7. Communication of 28 February 1995 from the Permanent Mission of Croatia to the International Atomic Energy Agency

    International Nuclear Information System (INIS)

    The Director General has received a note verbale of 28 February 1995 from the Permanent Mission of Croatia to the International Atomic Energy Agency providing information on the nuclear export policies and practices of the Government of Croatia

  8. Separation and Preconcentration of Ag(1) in Aqueous Samples by Flotation as an Ion-Associate Using Iodide and Ferroin Followed the Determination by Flame Atomic Absorption Spectrometry

    International Nuclear Information System (INIS)

    A simple method for separation/preconcentration and determination of Ag (1) in aqueous samples is described. The method is based on formation of an ion-associate between Ag (1)-iodide complex and ferroin, which can be floated at the interface of the aqueous/n-heptane phases. The flotation process was carried out using 500-ml aliquot of the aqueous solution and the floated layer was dissolved in 5 ml of 1 M HNO3 containing methanol (50% v/v) as the solvent. The Ag (1) content was then determined by flame atomic absorption spectrometry (FAAS). The method so could be considered as an enrichment process, was achieved to a quantitative feature, when the pH of the solution was adjusted to 4 and the concentrations of iodide and ferroin were about 3.2x10-4 M and 6.25x10-5 M, respectively. The LOD and RSD (n=7) were obtained 1.0x10-8 M and 2.4%, respectively. It was found that a large number of cations and anions even at high considerably foreign ion/Ag(1) ratios were not interfered. The method was applied satisfactorily to recovery of Ag(I) from different aqueous samples

  9. Chemical constraints governing the origin of metabolism: the thermodynamic landscape of carbon group transformations under mild aqueous conditions

    Science.gov (United States)

    Weber, Arthur L.

    2002-01-01

    The thermodynamics of organic chemistry under mild aqueous conditions was examined in order to begin to understand its influence on the structure and operation of metabolism and its antecedents. Free energies (deltaG) were estimated for four types of reactions of biochemical importance carbon-carbon bond cleavage and synthesis, hydrogen transfer between carbon groups, dehydration of alcohol groups, and aldo-keto isomerization. The energies were calculated for mainly aliphatic groups composed of carbon, hydrogen, and oxygen. The energy values showed (1) that generally when carbon-carbon bond cleavage involves groups from different functional group classes (i.e., carboxylic acids, carbonyl groups, alcohols, and hydrocarbons), the transfer of the shared electron-pair to the more reduced carbon group is energetically favored over transfer to the more oxidized carbon group, and (2) that the energy of carbon-carbon bond transformation is primarily determined by the functional group class of the group that changes oxidation state in the reaction (i.e., the functional group class of the group that donates the shared electron-pair during cleavage, or that accepts the incipient shared electron-pair during synthesis). In contrast, the energy of hydrogen transfer between carbon groups is determined by the functional group class of both the hydrogen-donor group and the hydrogen-acceptor group. From these and other observations we concluded that the chemistry involved in the origin of metabolism (and to a lesser degree modern metabolism) was strongly constrained by (1) the limited redox-based transformation energy of organic substrates that is readily dissipated in a few energetically favorable irreversible reactions; (2) the energy dominance of a few transformation half-reactions that determines whether carbon-carbon bond transformation (cleavage or synthesis) is energetically favorable (deltaG +3.5 kcal/mol); and (3) the dependence of carbon group transformation energy on the

  10. Cooperation Agreement. The Text of the Cooperation Agreement between the International Atomic Energy Agency and the ITER International Fusion Energy Organization

    International Nuclear Information System (INIS)

    The text of the Cooperation Agreement between the International Atomic Energy Agency and the ITER International Fusion Energy Organization is reproduced herein for the information of all Members. The Agreement entered into force on 13 October 2008 pursuant to Article 8

  11. Room temperature performance of 4 V aqueous hybrid supercapacitor using multi-layered lithium-doped carbon negative electrode

    Science.gov (United States)

    Makino, Sho; Yamamoto, Rie; Sugimoto, Shigeyuki; Sugimoto, Wataru

    2016-09-01

    Water-stable multi-layered lithium-doped carbon (LixC6) negative electrode using poly(ethylene oxide) (PEO)-lithium bis(trifluoromethansulfonyl)imide (LiTFSI) polymer electrolyte containing N-methyl-N-propylpiperidinium bis(trifluoromethansulfonyl)imide (PP13TFSI) ionic liquid was developed. Electrochemical properties at 60 °C of the aqueous hybrid supercapacitor using activated carbon positive electrode and a multi-layered LixC6 negative electrode (LixC6 | PEO-LiTFSI | LTAP) without PP13TFSI exhibited performance similar to that using Li anode (Li | PEO-LiTFSI | LTAP). A drastic decrease in ESR was achieved by the addition of PP13TFSI to PEO-LiTFSI, allowing room temperature operation. The ESR of the multi-layered LixC6 negative electrode with PEO-LiTFSI-PP13TFSI at 25 °C was 801 Ω cm2, which is 1/6 the value of the multi-layered Li negative electrode with PEO-LiTFSI (5014 Ω cm2). Charge/discharge test of the aqueous hybrid supercapacitor using multi-layered LixC6 negative electrode with PEO-LiTFSI-PP13TFSI at 25 °C afforded specific capacity of 20.6 mAh (g-activated carbon)-1 with a working voltage of 2.7-3.7 V, and good long-term capability up to 3000 cycles. Furthermore, an aqueous hybrid supercapacitor consisting of a high capacitance RuO2 nanosheet positive electrode and multi-layered LixC6 negative electrode with PEO-LiTFSI-PP13TFSI showed specific capacity of 196 mAh (g-RuO2)-1 and specific energy of 625 Wh (kg-RuO2)-1 in 2.0 M acetic acid-lithium acetate buffered solution at 25 °C.

  12. Immobilized nickel hexacyanoferrate on activated carbons for efficient attenuation of radio toxic Cs(I) from aqueous solutions

    International Nuclear Information System (INIS)

    Highlights: • Rice hulls and areca nut wastes are utilized to obtain activated carbons. • Nickel hexacyanoferrate is immobilized on activated carbon samples. • Materials are characterized by SEM–EDX and XRD data. • Materials are employed in attenuation of Cs(I) under batch and column studies. • Possible mechanism is deduced at solid/solution interface. - Abstract: The aim of this study is to immobilize nickel hexacyanoferrate onto the large surface of activated carbons (ACs) precursor to rice hulls and areca nut waste materials. These nickel hexacyanoferrate immobilized materials are then assessed in the effective attenuation of radio logically important cesium ions from aqueous solutions. The solid samples are characterized by the XRD analytical method and surface morphology is obtained from the SEM images. The batch reactor experiments show that an increase in sorptive pH (2.0–10.0) apparently not affecting the high percent uptake of Cs(I). Equilibrium modeling studies suggest that the data are reasonably and relatively fitted well to the Langmuir adsorption isotherm. Kinetic studies show that sorption process is fairly rapid and the kinetic data are fitted well to the pseudo-second order rate model. Increasing the background electrolyte concentration from 0.001 to 0.1 mol/L NaCl causes insignificant decrease in Cs(I) removal which infers the higher selectivity of these materials for Cs(I) from aqueous solutions. Further, the column reactor operations enable to obtain the breakthrough data which are then fitted to the Thomas non-linear equation as to obtain the loading capacity of column for Cs(I). The results show that the modified materials show potential applicability in the attenuation of radio toxic cesium from aqueous solution

  13. Sorption of a mixture of phenols in aqueous solution with activated carbon; Sorcion de una mezcla de fenoles en solucion acuosa con carbon activado

    Energy Technology Data Exchange (ETDEWEB)

    Mejia M, D.; Lopez M, B.E.; Iturbe G, J.L. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)

    2003-07-01

    The main objective of this work is the sorption of an aqueous mixture of phenol-4 chloro phenol of different concentrations in a molar relationship 1:1 in activated carbon of mineral origin of different nets (10, 20 and 30) and to diminish with it its presence in water. The experimental results show that the removal capacity depends so much of the surface properties of the sorbent like of the physical and chemical properties of the sorbate. In all the cases it was observed that in the aqueous systems of low concentration the 4-chloro phenol are removed in an approximate proportion of 1.2-4 times greater to than phenol, however to concentrations but high both they are removed approximately in the same proportion. (Author)

  14. DISLOCATION-SOLUTE ATOM INTERACTION IN ALUMINUM STUDIED BY AMPLITUDE-DEPENDENT INTERNAL FRICTION

    OpenAIRE

    Kosugi, T.; Kino, T.

    1985-01-01

    In order to get the information on the force-distance curve for the interaction between a dislocation and a solute atom, amplitude-dependent internal friction was measured at 1.7 - 30 K on Al-100 at ppm Zn and Al-50 at ppm Zn single crystals. The temperature dependence of applied strain under a constant decrement is the same for two concentrations with high accuracy. The data were analyzed by the thermally assisted break-away model for dislocations assuming several potential forms. In conclus...

  15. Earth sciences uranium geology, exploration and mining, hydrology, 1986-1998. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists sales publications of the International Atomic Energy Agency dealing with Earth Sciences issued during the period 1986-1998. Most publications are published in English. Proceedings of conferences, symposia and panels of experts may contain some papers in languages other than English (French, Russian or Spanish), but all these papers have abstracts in English. It should be noted that prices of books are quoted in Austrian Schillings. The prices do not include local taxes and are subject to change without notice. All books in this catalogue are 16 x 24 cm, paper-bound, unless otherwise stated

  16. Nuclear power, nuclear fuel cycle and waste management, 1986-1997. International Atomic Energy Agency publications

    International Nuclear Information System (INIS)

    This catalogue lists all sales publications of the International Atomic Energy Agency dealing with nuclear measurements, techniques and instrumentation, industrial applications, plasma physics and nuclear fusion and issued during the period of 1986-1997. Some earlier titles which form part of an established series or are still considered of importance have been included. Most publications are in English. Proceedings of conferences, symposia and panels of experts may contain papers in languages other than English, but all of these papers have abstracts in English

  17. Influence of supersaturated carbon on the diffusion of Ni in ferrite determined by atom probe tomography

    KAUST Repository

    Kresse, T.

    2013-09-01

    In patented and cold-drawn pearlitic steel wires dissociation of cementite occurs during mechanical deformation. In this study the influence of the carbon decomposition on the diffusion of nickel in ferrite is investigated by means of atom probe tomography. In the temperature range 423-523 K we observed a much smaller activation energy of Ni diffusion than for self-diffusion in body-centered cubic iron, indicating an increased vacancy density owing to enhanced formation of vacancy-carbon complexes. © 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

  18. Atomic layer deposition of amorphous iron phosphates on carbon nanotubes as cathode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    A non-aqueous approach was developed to synthesize iron phosphate cathode materials by the atomic layer deposition (ALD) technique. Deposition of iron phosphate thin films was achieved on nitrogen-doped carbon nanotubes (NCNTs) by combining ALD subcycles of Fe2O3 (ferrocene-ozone) and POx (trimethyl phosphate-water) at 200 – 350 °C. The thickness of iron phosphate thin films depends linearly on the ALD cycle, indicating their self-limiting growth behavior. The growth per cycle of iron phosphate thin films was determined to be ∼ 0.2, 0.4, 0.6, and 0.5 Å, at 200, 250, 300, and 350 °C, respectively. Characterization by SEM, TEM, and HRTEM techniques revealed uniform and conformal coating of amorphous iron phosphates on the surface of NCNTs. XANES analysis confirmed Fe−O−P bonding in the iron phosphates prepared by ALD. Furthermore, electrochemical measurement verified the high electrochemical activity of the amorphous iron phosphate as a cathode material in lithium-ion batteries. It is expected that the amorphous iron phosphate prepared by this facile and cost-effective ALD approach will find applications in the next generation of lithium-ion batteries and thin film batteries as either cathode materials or surface coating materials

  19. Origin of low-temperature shoulder internal friction peak of Snoek-Köster peak in a medium carbon high alloyed steel

    Science.gov (United States)

    Lu, Xianwen; Jin, Mingjiang; Zhao, Hongshan; Li, Wei; Jin, Xuejun

    2014-10-01

    A distinct internal friction peak located at the low-temperature shoulder of Snoek-Köster peak (LTS-SK) was found in Fe-0.39C-9.8Ni-1.56Si-2.0Mn steel and its evolution with respect to various aging treatments was investigated. The LTS-SK internal friction peak was found to occur when aged below 373 K. TEM observation confirmed that the ε-carbide precipitated beyond 373 K, providing an evidence that the LTS-SK peak cannot be caused by ε-carbide precipitation. The corresponding evolution on the S-K peak and thermoelectric power (TEP) illustrated that the carbon content in the solid solution decreases due to carbon atoms segregation on the surrounding dislocations during low-temperature aging. The origin of the LTS-SK peak is likely attributed to the interaction between the carbon atoms and twin boundaries in martensite.

  20. Carbon-13 magnetic relaxation rates or iron (III) complexes of some biogenic amines and parent compounds in aqueous solutions

    International Nuclear Information System (INIS)

    Spin-lattice relaxation rates (R1) from naturally occuring C-13 F.T. N.M.R. spectra of some catecholamines and parent compounds with Iron(III) at pD = 4 were determined in order to elucidate the molecular mechanism underlying their association in aqueous solutions. Complexation was observed only for catecholic ligands. The R1 values were used to calculate iron-carbon scaled distances, and two complexation models were proposed where the catecholic function binds Fe(III) in the first and second coordination spheres respectively. The latter case was shown to be the consistent with the molecular geometries. (orig.)

  1. Covalent and non-covalent functionalization and solubilization of double-walled carbon nanotubes in nonpolar and aqueous media

    Indian Academy of Sciences (India)

    L S Panchakarla; A Govindaraj

    2008-11-01

    Double-walled carbon nanotubes (DWNTs) have been functionalized by both covalent and non-covalent means. Covalent functionalization has been carried out by attaching an aliphatic amide function to DWNTs which enable solubilization in non-polar solvents. Solubilization in non-polar solvents has also been accomplished by non-covalent functionalization by using 1-pyrenebutanoicacid succinimidyl ester (PYBS). Non-covalent functionalization of DWNTs has been carried out by using polyethylene glycol (PEG) and polyoxyethylene(40)nonylphenyl ether (IGPAL), both of which enable solubilization in aqueous media. These functionalized DWNTs have been characterized by transmission electron microscopy, IR and Raman spectroscopy.

  2. Kinetics of the Removal of Chromium Complex Dye from Aqueous Solutions Using Activated Carbons and Polymeric Adsorbent

    OpenAIRE

    Eglė Kazlauskienė; Danutė Kaušpėdienė

    2011-01-01

    The kinetics of the removal of chromium complex dye (Lanasyn Navy M-DNL) from aqueous solutions using polymeric adsorbent Macronet MN 200 (MN 200) as an alternative option for activated carbon Norit RB 0.8 CC (AC) was studied in the batch system. The residual colour of dye solution treated with AC or MN 200 strongly depends on solution pH with lower values at acidic pH when a positively charged surface net is favourable for the adsorption of the dye anion. The removal of dye using MN 200 was ...

  3. IMPROVED FABRICATION METHOD FOR CARBON NANOTUBE PROBE OF ATOMIC FORCE MICROSCOPY(AFM)

    Institute of Scientific and Technical Information of China (English)

    XU Zongwei; DONG Shen; GUO Liqiu; ZHAO Qingliang

    2006-01-01

    An improved arc discharge method is developed to fabricate carbon nanotube probe of atomic force microscopy (AFM) here. First, silicon probe and carbon nanotube are manipulated under an optical microscope by two high precision microtranslators. When silicon probe and carbon nanotube are very close, several tens voltage is applied between them. And carbon nanotube is divided and attached to the end of silicon probe, which mainly due to the arc welding function.Comparing with the arc discharge method before, the new method here needs no coat silicon probe with metal film in advance, which can greatly reduce the fabrication's difficulty. The fabricated carbon nanotube probe shows good property of higher aspect ratio and can more accurately reflect the true topography of silicon grating than silicon probe. Under the same image drive force, carbon nanotube probe had less indentation depth on soft triblock copolymer sample than silicon probe. This showed that carbon nanotube probe has lower spring constant and less damage to the scan sample than silicon probe.

  4. Synthesis and utilization of a novel carbon nanotubes supported nanocables for the adsorption of dyes from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wei; Jiang, Xinyu [School of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Chen, Xiaoqing, E-mail: xqchen@csu.edu.cn [School of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Collaborative Innovation Center of Resource-conserving & Environment-friendly Society and Ecological Civilization (China)

    2015-09-15

    Using multiwalled carbon nanotubes(MWCNTs) as mechanical support and glucose as carbon resource, a hydrothermal carbonization route was designed for the synthesis of MWCNTs@carbon nanocables with tunable diameter and length. MWCNTs are firstly used as templates for the formation of carbon-rich composite nanocables, and the diameter of the nanocables could be tailored through adjusting the hydrothermal time or the ratio of MWCNTs and glucose. Owing to abundant superficial oxygen-containing functional groups, porous surface and remarkable reactivity, the as-synthesized nanocables are capable of efficiently adsorbing cationic dye methylene blue (MB) and crystal violet (CV). Furthermore, the optimum adsorption conditions, kinetics, adsorption isotherms and adsorption thermodynamics of dyes were studied systematically. Additionally, the maximum adsorption capacities calculated from data analysis (298.5 mg/g for MB and 228.3 mg/g for CV) are significant higher than those of raw MWCNTs and some other adsorbents reported previously, which provides strong evidence for using MWCNTs@carbon nanocables as adsorbent to remove dyes from aqueous solutions. - Graphical abstract: MWCNTs@carbon nanocables has been successfully fabricated by a hydrothermal carbonization method. The as-synthesized novel samples were used as adsorbents and exhibited high adsorption capacity on MB and CV. - Highlights: • A simple, cost-effective and “green” method for the synthesis of the material. • The diameter and length of the material are relatively easy to control. • The surface has large oxygen-containing groups and preferable chemical reactivity. • Compared with raw MWCNTs and some other adsorbents, the adsorption capacity is much high.

  5. Synthesis and utilization of a novel carbon nanotubes supported nanocables for the adsorption of dyes from aqueous solutions

    International Nuclear Information System (INIS)

    Using multiwalled carbon nanotubes(MWCNTs) as mechanical support and glucose as carbon resource, a hydrothermal carbonization route was designed for the synthesis of MWCNTs@carbon nanocables with tunable diameter and length. MWCNTs are firstly used as templates for the formation of carbon-rich composite nanocables, and the diameter of the nanocables could be tailored through adjusting the hydrothermal time or the ratio of MWCNTs and glucose. Owing to abundant superficial oxygen-containing functional groups, porous surface and remarkable reactivity, the as-synthesized nanocables are capable of efficiently adsorbing cationic dye methylene blue (MB) and crystal violet (CV). Furthermore, the optimum adsorption conditions, kinetics, adsorption isotherms and adsorption thermodynamics of dyes were studied systematically. Additionally, the maximum adsorption capacities calculated from data analysis (298.5 mg/g for MB and 228.3 mg/g for CV) are significant higher than those of raw MWCNTs and some other adsorbents reported previously, which provides strong evidence for using MWCNTs@carbon nanocables as adsorbent to remove dyes from aqueous solutions. - Graphical abstract: MWCNTs@carbon nanocables has been successfully fabricated by a hydrothermal carbonization method. The as-synthesized novel samples were used as adsorbents and exhibited high adsorption capacity on MB and CV. - Highlights: • A simple, cost-effective and “green” method for the synthesis of the material. • The diameter and length of the material are relatively easy to control. • The surface has large oxygen-containing groups and preferable chemical reactivity. • Compared with raw MWCNTs and some other adsorbents, the adsorption capacity is much high

  6. The atomic configuration of graphene/vanadium carbide interfaces in vanadium carbide-encapsulating carbon nanocapsules.

    Science.gov (United States)

    Yazaki, Gaku; Matsuura, Daisuke; Kizuka, Tokushi

    2014-03-01

    Carbon nanocapsules (CNCs) encapsulating vanadium carbide (VC) nanocrystals with a NaCI structure were synthesized by a gas-evaporation method using arc-discharge heating. The CNCs were observed by high-resolution transmission electron microscopy. The VC nanocrystals within the nanospaces of CNCs were truncated by low-index facets and were coated with several graphene layers, forming graphene/VC interfaces. The atomic configuration and interlayer spacings at the interfaces were found. PMID:24745251

  7. Localised quantum states of atomic and molecular particles physisorbed on carbon-based nanoparticles

    Czech Academy of Sciences Publication Activity Database

    Kaprálová-Žďánská, Petra Ruth; Trachta, Michal; Bludský, Ota; Špirko, Vladimír

    2014-01-01

    Roč. 141, č. 11 (2014), "114702-1"-"114702-10". ISSN 0021-9606 R&D Projects: GA ČR GAP205/11/0571; GA ČR GAP208/11/0436; GA ČR GAP208/10/0725 Institutional support: RVO:68378271 ; RVO:61388963 Keywords : periodic structure * carbon nanostructures * graphene * quantum mechanics * physisorbed Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders Impact factor: 2.952, year: 2014

  8. Sorption of a phenols mixture in aqueous solution with activated carbon; Sorcion de una mezcla de fenoles en solucion acuosa con carbon activado

    Energy Technology Data Exchange (ETDEWEB)

    Mejia M, D

    2004-07-01

    The constant population growth and the quick industrialization have caused severe damages to our natural aquifer resources for a great variety of organic and inorganic pollutants. Among these they are those phenol compounds that are highly toxic, resistant (to the degradation chemistry) and poorly biodegradable. The phenolic compounds is used in a great variety of industries, like it is the production of resins, nylon, plastifiers, anti-oxidants, oil additives, drugs, pesticides, colorants, explosives, disinfectants and others. The disseminated discharges or effluents coming from the industrial processes toward lakes and rivers are causing a growing adverse effect in the environment, as well as a risk for the health. Numerous studies exist on the phenols removal and phenols substituted for very varied techniques, among them they are the adsorption in activated carbon. This finishes it has been used successfully for the treatment of residual waters municipal and industrial and of drinking waters and it is considered as the best technique available to eliminate organic compounds not biodegradable and toxic present in aqueous solution (US EPA, 1991). However a little information exists on studies carried out in aqueous systems with more of a phenolic compound. The activated carbon is broadly used as adsorbent due to its superficial properties in the so much treatment of water as of aqueous wastes, adsorbent for the removal of organic pollutants. The main objective of this work is the adsorption of a aqueous mixture of phenol-4 chloro phenol of different concentrations in activated carbon of mineral origin of different meshes and to diminish with it their presence in water. The experiments were carried out for lots, in normal conditions of temperature and pressure. The experimental results show that the removal capacity depends so much of the superficial properties of the sorbent like of the physical properties and chemical of the sorbate. The isotherms were carried

  9. Chemical and structural evaluation of activated carbon prepared from jute sticks for Brilliant Green dye removal from aqueous solution.

    Science.gov (United States)

    Asadullah, Mohammad; Asaduzzaman, Mohammad; Kabir, Mohammad Shajahan; Mostofa, Mohammad Golam; Miyazawa, Tomohisa

    2010-02-15

    Activated carbons have been prepared from jute sticks by chemical activation using ZnCl(2) and physical activation using steam for the removal of Brilliant Green dye from aqueous solution. The activated carbons and charcoal prepared from jute sticks were characterized by evaluating the surface chemistry, structural features and surface morphology. The maximum BET surface area was obtained to be 2304 m(2)/g for chemical activated carbon (ACC) while it is 730 and 80 m(2)/g for steam activated carbon (ACS) and charcoal, respectively. The FT-IR spectra exhibited that the pyrolysis and steam activation of jute sticks resulted in the release of aliphatic and O-containing functional groups by thermal effect. However, the release of functional groups is the effect of chemical reaction in the ZnCl(2) activation process. A honeycomb-type carbon structure in ACC was formed as observed on SEM images. Although charcoal and ACC were prepared at 500 degrees C the ACC exhibited much lower Raman sensitivity due to the formation of condensed aromatic ring systems. Due to high surface area and high porous structure with abundance of functional groups, the ACC adsorbed dye molecules with much higher efficiency than those of ACS and charcoal. PMID:19815339

  10. Removal of Cu(II) from aqueous solution using the rice husk carbons prepared by the physical activation process

    International Nuclear Information System (INIS)

    The adsorption of Cu(II) from aqueous solution by carbons prepared from rice husk through pyrolysis and steam activation was studied. The rice husk carbon was characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM), and its pore structure was also examined. After comparing different characteristics of the carbons prepared under different conditions and their adsorption abilities of Cu(II), the optimum temperature for pyrolysis and steam activation was chosen as 700 and 750 oC, respectively, using 3% (V/V) steam as the best activation gas. It was found that the Cu(II) adsorption on the rice husk derived carbons was pH and temperature dependent with an optimum pH value of 5.0, and an equilibrium time of 24 h. The adsorption kinetics and isotherms of Cu(II) by the rice husk derived carbons were also investigated under four different temperatures, and good correlation coefficients were obtained for the pseudo-second-order kinetic models, and the Langmuir isotherm model fitted very well with the experimental data. The mean free energy E (kJ mol-1) obtained in the Dubinin-Radushkevitch (D-R) adsorption isortherm equation indicated a chemical ion-exchange mechanism. Several thermodynamic parameters were also caculated to predict the nature of adsorption process.

  11. MD investigation of the collective carbon atom behavior of a (17, 0) zigzag single wall carbon nanotube under axial tensile strain

    International Nuclear Information System (INIS)

    The collective dynamic behavior of carbon atoms of a (17, 0) zigzag single wall carbon nanotube is investigated under tensile strains by molecular dynamics (MD) simulations. The 'slip vector' parameter is used to study the collective motion of a group of atoms and the deformation behavior in three different directions (axial, radial, and tangential) of a (17, 0) carbon nanotube. The variations of radial slip vectors indicate almost all carbon atoms of the (17, 0) carbon nanotube will stay on the cylindrical surface before the yielding of the single wall carbon nanotube (SWNT). Furthermore, the tangential vectors show kinking deformation for the (17, 0) zigzag tube only rarely appears when the crack occurs. Non-symmetrical deformation around a carbon atom along the axial direction also can be found. The variations in the slip vector values of each atom display a symmetrical crack along the horizontal direction and normal to the tube axis. Chain-like structures with 3-4 atoms can be observed, with the number of chain-like structures decreasing before the breakage of the SWNT. The mechanical properties and dynamic behavior of a (17, 0) zigzag SWNT under tensile strain are also compared with that of a (10, 10) armchair tube in our previous study (Weng et al. 2009).

  12. Electronic transport in large systems through a QUAMBO-NEGF approach: Application to atomic carbon chains

    International Nuclear Information System (INIS)

    The conductance of single-atom carbon chain (SACC) between two zigzag graphene nanoribbons (GNR) is studied by an efficient scheme utilizing tight-binding (TB) parameters generated via quasi-atomic minimal basis set orbitals (QUAMBOs) and non-equilibrium Green's function (NEGF). Large systems (SACC contains more than 50 atoms) are investigated and the electronic transport properties are found to correlate with SACC's parity. The SACCs provide a stable off or on state in broad energy region (0.1-1 eV) around Fermi energy. The off state is not sensitive to the length of SACC while the corresponding energy region decreases with the increase of the width of GNR. -- Highlights: → Graphene has many superior electronic properties. → First-principles calculation are accurate but limited to system size. → QUAMBOs construct tight-binding parameters with spatial localization, and then use divide-and-conquer method. → SACC (single carbon atom chain): structure and transport show even-odd parity, and long chains are studied.

  13. Negotiating supranational rules. The genesis of the International Atomic Energy Agency safeguards system

    International Nuclear Information System (INIS)

    The object of this study is the evolution from 1954-56 up until the mid-1970s of the nuclear safeguards system administered by the International Atomic Energy Agency (IAEA) in Vienna. The main aim of the study is not to describe the IAEA safeguards system as such. The focus will be on analysing the arguments advanced in the various negotiations, and the main objective will be to single out the factors determining the result. In the course of the time span under study two international treaties were negotiated which were decisive for the development of international nuclear safeguards. These were the IAEA Stature (1956) and the Non-Proliferation Treaty (1968). The Statue as well as the NPT contain articles on international nuclear safeguards. These articles limit themselves to spelling out the safeguards principles. It was thus left to the IAEA Board of Governors to develop the safeguards procedures in detail. Two IAEA safeguards documents were negotiated between 1959 and 1965 in order to implement the safeguards article of the Statue. The safeguards requirements of the NPT were spelled out in a new model agreement in 1972. 58 refs

  14. Negotiating supranational rules. The genesis of the International Atomic Energy Agency safeguards system

    Energy Technology Data Exchange (ETDEWEB)

    Forland, A.

    1997-12-31

    The object of this study is the evolution from 1954-56 up until the mid-1970s of the nuclear safeguards system administered by the International Atomic Energy Agency (IAEA) in Vienna. The main aim of the study is not to describe the IAEA safeguards system as such. The focus will be on analysing the arguments advanced in the various negotiations, and the main objective will be to single out the factors determining the result. In the course of the time span under study two international treaties were negotiated which were decisive for the development of international nuclear safeguards. These were the IAEA Stature (1956) and the Non-Proliferation Treaty (1968). The Statue as well as the NPT contain articles on international nuclear safeguards. These articles limit themselves to spelling out the safeguards principles. It was thus left to the IAEA Board of Governors to develop the safeguards procedures in detail. Two IAEA safeguards documents were negotiated between 1959 and 1965 in order to implement the safeguards article of the Statue. The safeguards requirements of the NPT were spelled out in a new model agreement in 1972. 58 refs.

  15. Atom interferometric measurement of ``Big G'' on the International Space Station

    Science.gov (United States)

    Ashwood, Elizabeth; Kurkcuoglu, Doga Murat; Clark, Charles W.; Edwards, Mark

    2016-05-01

    Recent measurements of Newton's universal gravitational constant (``Big G'') using atom interferometric methods have increased the uncertainty in the value of this important fundamental constant. We have developed tools for rapid simulation and evaluation of atom interferometer (AI) schemes that can be implemented in the Cold Atom Laboratory to be deployed to the International Space Station (ISS) in 2017. We have approximated the solution of the rotating-frame Gross-Pitaevskii equation in both one and three dimensions by using the Lagrangian Variational Method (LVM). The LVM trial wave function is a sum of Nc Gaussian clouds and we have derived equations of motion for the centers, widths, and phase parameters of these clouds. These equations of motion can be rapidly solved for many different AI designs enabling the estimation interferometer sensitivity and the effects of errors. We present two potential schemes as for measuring ``Big G'' on the ISS. These include a Mach-Zehnder-like scheme as well as a design similar to a Foucault Pendulum. Supported by NSF Grant PHY-1413768.

  16. Significant Performance Enhancement in Asymmetric Supercapacitors based on Metal Oxides, Carbon nanotubes and Neutral Aqueous Electrolyte

    OpenAIRE

    Arvinder Singh; Amreesh Chandra

    2015-01-01

    Amongst the materials being investigated for supercapacitor electrodes, carbon based materials are most investigated. However, pure carbon materials suffer from inherent physical processes which limit the maximum specific energy and power that can be achieved in an energy storage device. Therefore, use of carbon-based composites with suitable nano-materials is attaining prominence. The synergistic effect between the pseudocapacitive nanomaterials (high specific energy) and carbon (high specif...

  17. The solubility of very low concentratiions of carbon monoxide in aqueous solution

    OpenAIRE

    Meadows, R. W.; Spedding, D. J.

    2011-01-01

    The solubility of carbon monoxide in natural waters has been determined when the partial pressure of carbon monoxide in the gas phase approaches atmospheric concentrations. For both pure water and seawater the solubilities were found to be more than eight times the values which have previously been observed with an atmosphere of pure carbon monoxide present. Carbon monoxide therefore does not obey Henry's law over the pressure range from approximately 10?5 atmospheres to greater than one atmo...

  18. Noble metals as permanent chemical modifiers for the determination of mercury in environmental reference materials using solid sampling graphite furnace atomic absorption spectrometry and calibration against aqueous standards

    Science.gov (United States)

    da Silva, Alessandra Furtado; Welz, Bernhard; Curtius, Adilson J.

    2002-12-01

    Iridium, palladium, rhodium and ruthenium, thermally deposited on the platform, were investigated as permanent modifiers for the determination of mercury in ash, sludge, marine and river sediment reference materials, ground to a particle size of 50 μm, using solid sampling graphite furnace atomic absorption spectrometry. A total mass of 250 μg of each modifier was applied using 25 injections of 20 μl of modifier solution (500 mg l -1), and executing a temperature program for modifier conditioning after each injection. The performance of palladium was found to be most consistent, taking the characteristic mass as the major criterion, resulting in an excellent correlation between the measured integrated absorbance values and the certified mercury contents. Mercury was found to be lost in part from aqueous solutions during the drying stage in the presence of all the investigated permanent modifiers, as well as in the presence of the palladium and magnesium nitrates modifier added in solution. A loss-free determination of mercury in aqueous solutions could be reached only after the addition of potassium permanganate, which finally made possible the use of aqueous standards for the direct analysis of solid samples. A characteristic mass of 55-60 pg Hg was obtained for the solid samples, using Pd as a permanent modifier, and also in aqueous solutions after the addition of permanganate. The results obtained for mercury in ash, sludge and sediment reference materials, using direct solid sapling and calibration against aqueous standards, as well as the detection limit of 0.2 mg kg -1 were satisfactory for a routine procedure.

  19. Noble metals as permanent chemical modifiers for the determination of mercury in environmental reference materials using solid sampling graphite furnace atomic absorption spectrometry and calibration against aqueous standards

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Alessandra Furtado da; Welz, Bernhard; Curtius, Adilson J

    2002-12-02

    Iridium, palladium, rhodium and ruthenium, thermally deposited on the platform, were investigated as permanent modifiers for the determination of mercury in ash, sludge, marine and river sediment reference materials, ground to a particle size of 50 {mu}m, using solid sampling graphite furnace atomic absorption spectrometry. A total mass of 250 {mu}g of each modifier was applied using 25 injections of 20 {mu}l of modifier solution (500 mg l{sup -1}), and executing a temperature program for modifier conditioning after each injection. The performance of palladium was found to be most consistent, taking the characteristic mass as the major criterion, resulting in an excellent correlation between the measured integrated absorbance values and the certified mercury contents. Mercury was found to be lost in part from aqueous solutions during the drying stage in the presence of all the investigated permanent modifiers, as well as in the presence of the palladium and magnesium nitrates modifier added in solution. A loss-free determination of mercury in aqueous solutions could be reached only after the addition of potassium permanganate, which finally made possible the use of aqueous standards for the direct analysis of solid samples. A characteristic mass of 55-60 pg Hg was obtained for the solid samples, using Pd as a permanent modifier, and also in aqueous solutions after the addition of permanganate. The results obtained for mercury in ash, sludge and sediment reference materials, using direct solid sapling and calibration against aqueous standards, as well as the detection limit of 0.2 mg kg{sup -1} were satisfactory for a routine procedure.

  20. Accessibility, searchability, transparency and engagement of soil carbon data: The International Soil Carbon Network

    Science.gov (United States)

    Harden, Jennifer W.; Hugelius, Gustaf; Koven, Charlie; Sulman, Ben; O'Donnell, Jon; He, Yujie

    2016-04-01

    Soils are capacitors for carbon and water entering and exiting through land-atmosphere exchange. Capturing the spatiotemporal variations in soil C exchange through monitoring and modeling is difficult in part because data are reported unevenly across spatial, temporal, and management scales and in part because the unit of measure generally involves destructive harvest or non-recurrent measurements. In order to improve our fundamental basis for understanding soil C exchange, a multi-user, open source, searchable database and network of scientists has been formed. The International Soil Carbon Network (ISCN) is a self-chartered, member-based and member-owned network of scientists dedicated to soil carbon science. Attributes of the ISCN include 1) Targeted ISCN Action Groups which represent teams of motivated researchers that propose and pursue specific soil C research questions with the aim of synthesizing seminal articles regarding soil C fate. 2) Datasets to date contributed by institutions and individuals to a comprehensive, searchable open-access database that currently includes over 70,000 geolocated profiles for which soil C and other soil properties. 3) Derivative products resulting from the database, including depth attenuation attributes for C concentration and storage; C storage maps; and model-based assessments of emission/sequestration for future climate scenarios. Several examples illustrate the power of such a database and its engagement with the science community. First, a simplified, data-constrained global ecosystem model estimated a global sensitivity of permafrost soil carbon to climate change (g sensitivity) of -14 to -19 Pg C °C-1 of warming on a 100 years time scale. Second, using mathematical characterizations of depth profiles for organic carbon storage, C at the soil surface reflects Net Primary Production (NPP) and its allotment as moss or litter, while e-folding depths are correlated to rooting depth. Third, storage of deep C is highly

  1. Sorption of Ni(II), Cu(II) and Fe(III) ions from Aqueous Solutions Using Activated Carbon

    International Nuclear Information System (INIS)

    An activated carbon was tested for its ability to remove transition metal ions from aqueous solutions. Physical, chemical and liquid-phase adsorption characterizations of the carbon were done following standard procedures. Studies on the removal of Ni(II), Cu(II) and Fe(III) ions were attempted by varying adsorbate dose, pH of the metal ion solution and time in batch mode. The equilibrium adsorption data were fitted with Freundlich and Langmuir and the isotherm constants were evaluated, equilibrium time of the different three metal ions were determined. pH was found to have a significant role to play in the adsorption. The processes were endothermic and the thermodynamic parameters were evaluated. Desorption studies indicate that ion-exchange mechanism is operating

  2. Enhanced dispersion stability and mobility of carboxyl-functionalized carbon nanotubes in aqueous solutions through strong hydrogen bonds

    International Nuclear Information System (INIS)

    Dispersion of carbon nanotubes has been heavily studied due to its importance for their technical applications, toxic effects, and environmental impacts. Common electrolytes, such as sodium chloride and potassium chloride, promote agglomeration of nanoparticles in aqueous solutions. On the contrary, we discovered that acetic electrolytes enhanced the dispersion of multi-walled carbon nanotubes (MWCNTs) with carboxyl functional group through the strong hydrogen bond, which was confirmed by UV–Vis spectrometry, dispersion observations and aerosolization-quantification method. When concentrations of acetate electrolytes such as ammonium acetate (CH3CO2NH4) and sodium acetate (CH3CO2Na) were lower than 0.03 mol per liter, MWCNT suspensions showed better dispersion and had higher mobility in porous media. The effects by the acetic environment are also applicable to other nanoparticles with the carboxyl functional group, which was demonstrated with polystyrene latex particles as an example

  3. High-performance aqueous asymmetric supercapacitor based on carbon nanofibers network and tungsten trioxide nanorod bundles electrodes

    International Nuclear Information System (INIS)

    The demand for high-performance energy storage devices such as supercapacitors and lithium-ion batteries has been increasing to meet the application requirements of renewable energy systems. Here, high energy density aqueous asymmetric supercapacitor (ASC) is assembled based on carbon nanofibers (CNF) network positive electrode and tungsten trioxide (WO3) nanorod bundles negative electrode. Polyaniline-based CNF are prepared by direct carbonization of polyaniline nanofibers. WO3 nanorod bundles are synthesized via a simple sodium chloride assisted hydrothermal process. The CNF//WO3 ASC device operates with a voltage of 1.6 V and achieved a high energy density of 35.3 Wh kg−1 at a power density of 314 W kg−1. Furthermore, the device shows an excellent cycling performance with capacitance retention of 88% after 1000 cycles

  4. Enhanced dispersion stability and mobility of carboxyl-functionalized carbon nanotubes in aqueous solutions through strong hydrogen bonds

    Energy Technology Data Exchange (ETDEWEB)

    Bahk, Yeon Kyoung; He, Xu; Gitsis, Emmanouil; Kuo, Yu-Ying [ETH Zurich, Institute of Environmental Engineering (Switzerland); Kim, Nayoung [EMPA, Building Energy Materials and Components (Switzerland); Wang, Jing, E-mail: jing.wang@ifu.baug.ethz.ch [ETH Zurich, Institute of Environmental Engineering (Switzerland)

    2015-10-15

    Dispersion of carbon nanotubes has been heavily studied due to its importance for their technical applications, toxic effects, and environmental impacts. Common electrolytes, such as sodium chloride and potassium chloride, promote agglomeration of nanoparticles in aqueous solutions. On the contrary, we discovered that acetic electrolytes enhanced the dispersion of multi-walled carbon nanotubes (MWCNTs) with carboxyl functional group through the strong hydrogen bond, which was confirmed by UV–Vis spectrometry, dispersion observations and aerosolization-quantification method. When concentrations of acetate electrolytes such as ammonium acetate (CH{sub 3}CO{sub 2}NH{sub 4}) and sodium acetate (CH{sub 3}CO{sub 2}Na) were lower than 0.03 mol per liter, MWCNT suspensions showed better dispersion and had higher mobility in porous media. The effects by the acetic environment are also applicable to other nanoparticles with the carboxyl functional group, which was demonstrated with polystyrene latex particles as an example.

  5. Removal of cationic dyes from aqueous solution using magnetic multi-wall carbon nanotube nanocomposite as adsorbent

    International Nuclear Information System (INIS)

    A magnetic multi-wall carbon nanotube (MMWCNT) nanocomposite was synthesized and was used as an adsorbent for removal of cationic dyes from aqueous solutions. The MMWCNT nanocomposite was composed of commercial multi-wall carbon nanotubes and iron oxide nanoparticles. The properties of this magnetic adsorbent were characterized by scanning electron microscopy, X-ray diffraction and BET surface area measurements. Adsorption characteristics of the MMWCNT nanocomposite adsorbent were examined using methylene blue, neutral red and brilliant cresyl blue as adsorbates. Experiments were carried out to investigate adsorption kinetics, adsorption capacity of the adsorbent and the effect of adsorption dosage and solution pH values on the removal of cationic dyes. Kinetic data were well fitted by a pseudo second-order model. Freundlich model was used to study the adsorption isotherms. The prepared MMWCNT adsorbent displayed the main advantage of separation convenience compared to the present adsorption treatment.

  6. Synthesis of magnetic nanoporous carbon from metal-organic framework for the fast removal of organic dye from aqueous solution

    Science.gov (United States)

    Jiao, Caina; Wang, Yanen; Li, Menghua; Wu, Qiuhua; Wang, Chun; Wang, Zhi

    2016-06-01

    In this paper, a magnetic nanoporous carbon (Fe3O4/NPC) was successfully synthesized by using MOF-5 as carbon precursor and Fe salt as magnetic precursor. The texture properties of the as-synthesized nanocomposite were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibration sample magnetometer (VSM), and N2 adsorption-desorption isotherms. The Fe3O4/NPC had a high surface area with strong magnetic strength. Its adsorption behavior was tested by its adsorption capacity for the removal of methylene blue from aqueous solution. The results demonstrated that the Fe3O4/NPC had a high adsorption capacity, rapid adsorption rate, and easy magnetic separabilty. Moreover, the adsorbent could be easily regenerated by washing it with ethanol. The Fe3O4/NPC can be used as a good alternative for the effective removal of organic dyes from wastewater.

  7. Sixteenth International Conference on the physics of electronic and atomic collisions

    International Nuclear Information System (INIS)

    This report contains abstracts of papers on the following topics: photons, electron-atom collisions; electron-molecule collisions; electron-ion collisions; collisions involving exotic species; ion- atom collisions, ion-molecule or atom-molecule collisions; atom-atom collisions; ion-ion collisions; collisions involving rydberg atoms; field assisted collisions; collisions involving clusters and collisions involving condensed matter

  8. Sixteenth International Conference on the physics of electronic and atomic collisions

    Energy Technology Data Exchange (ETDEWEB)

    Dalgarno, A.; Freund, R.S.; Lubell, M.S.; Lucatorto, T.B. (eds.)

    1989-01-01

    This report contains abstracts of papers on the following topics: photons, electron-atom collisions; electron-molecule collisions; electron-ion collisions; collisions involving exotic species; ion- atom collisions, ion-molecule or atom-molecule collisions; atom-atom collisions; ion-ion collisions; collisions involving rydberg atoms; field assisted collisions; collisions involving clusters and collisions involving condensed matter.

  9. Investigation of the Interactions and Bonding between Carbon and Group VIII Metals at the Atomic Scale.

    Science.gov (United States)

    Zoberbier, Thilo; Chamberlain, Thomas W; Biskupek, Johannes; Suyetin, Mikhail; Majouga, Alexander G; Besley, Elena; Kaiser, Ute; Khlobystov, Andrei N

    2016-03-23

    The nature and dynamics of bonding between Fe, Ru, Os, and single-walled carbon nanotubes (SWNTs) is studied by aberration-corrected high-resolution transmission electron microscopy (AC-HRTEM). The metals catalyze a wide variety of different transformations ranging from ejection of carbon atoms from the nanotube sidewall to the formation of hollow carbon shells or metal carbide within the SWNT, depending on the nature of the metal. The electron beam of AC-HRTEM serves the dual purpose of providing energy to the specimen and simultaneously enabling imaging of chemical transformations. Careful control of the electron beam parameters, energy, flux, and dose allowed direct comparison between the metals, demonstrating that their chemical reactions with SWNTs are determined by a balance between the cohesive energy of the metal particles and the strength of the metal-carbon σ- or π-bonds. The pathways of transformations of a given metal can be drastically changed by applying different electron energies (80, 40, or 20 keV), thus demonstrating AC-HRTEM as a new tool to direct and study chemical reactions. The understanding of interactions and bonding between SWNT and metals revealed by AC-HRTEM at the atomic level has important implications for nanotube-based electronic devices and catalysis. PMID:26848826

  10. Methods of removal of tritium from aqueous effluent: a review of international research and development

    International Nuclear Information System (INIS)

    Tritium is formed in thermal nuclear reactors both by neutron activation of elements such as deuterium and lithium and by ternary fission in the fuel. It is a weak beta-emitter with a short half-life, 12.3 years, and its radiological significance in reactor discharges is very low. In heavy-water-cooled and -moderated reactors, such as the CANDU stations, the tritium concentration in the moderator is sufficiently high to cause a potential hazard to operators, and so a major research and development programme has been carried out on processes to remove the tritium. Detritiation of light water has also been the subject of major R and D effort world-wide, because reprocessing operations can generate significant quantities of tritium in liquid waste, and high concentrations of tritium may arise in some aqueous streams in fusion reactors. This Report presents a review of the methods that have been proposed, studied and developed for removal of tritium from light and heavy water: the principles of individual methods are discussed, and the current status of their development is reviewed. (author)

  11. Adsorption and manipulation of carbon onions on highly oriented pyrolytic graphite studied with atomic force microscopy

    International Nuclear Information System (INIS)

    Carbon onions produced by DC arc discharge method were deposited on highly oriented pyrolytic graphite (HOPG) surface and their adsorption and manipulation was studied using an atomic force microscopy (AFM). Well-dispersed adsorption of carbon onions on HOPG surface was obtained and aggregations of onions were not observed. The van der Waals interaction between the onion and HOPG surface and that between two onions, were calculated and discussed using Hamaker's theory. The manipulation of adsorbed onions on HOPG surface was realized using the AFM in both the raster mode and the vector mode. The controllability and precision of two manipulation modes were compared and the vector mode manipulation was found superior, and is a useful technique for the construction of nano-scale devices based on carbon onions

  12. Atom Probe Tomography Examination of Carbon Redistribution in Quenched and Tempered 4340 Steel

    Energy Technology Data Exchange (ETDEWEB)

    Clarke, Amy J. [Los Alamos National Laboratory; Miller, Michael K. [ORNL; Alexander, David J. [Los Alamos National Laboratory; Field, Robert D. [Los Alamos National Laboratory; Clarke, Kester D. [Los Alamos National Laboratory

    2012-08-07

    Quenching and tempering produces a wide range of mechanical properties in medium carbon, low alloyed steels - Study fragmentation behavior as a function of heat-treatment. Subtle microstructural changes accompany the mechanical property changes that result from quenching and tempering - Characterize the location and distribution of carbon and alloying elements in the microstructure using atom probe tomography (APT). Perform complementary transmission electron microscopy (TEM). Tempering influences the mechanical properties and fragmentation of quenched 4340 (hemi-shaped samples). APT revealed carbon-enriched features that contain a maximum of {approx}12-14 at.% carbon after quenching to RT (the level of carbon is perhaps associated with the extent of autotempering). TEM confirmed the presence of twinned martensite and indicates {var_epsilon} ({eta}) transition carbides after oil quenching to RT. Tempering at 325 C resulted in carbon-enriched plates (> 25 at.% C) with no significant element partitioning (transition carbides?). Tempering at 450 C and 575 C resulted in cementite ({approx} 25 at.% C) during late stage tempering; Cr, Mn, Mo partitioned to cementite and Si partitioned to ferrite. Tempering at 575 C resulted in P segregation at cementite interfaces and the formation of Cottrell atmospheres.

  13. Surface modification of activated carbon for enhanced adsorption of perfluoroalkyl acids from aqueous solutions.

    Science.gov (United States)

    Zhi, Yue; Liu, Jinxia

    2016-02-01

    The objective of the research was to examine the effect of increasing carbon surface basicity on uptake of perfluorooctane sulfonic (PFOS) and carboxylic acids (PFOA) by activated carbon. Granular activated carbons made from coal, coconut shell, wood, and phenolic-polymer-based activated carbon fibers were modified through high-temperature and ammonia gas treatments to facilitate systematical evaluation of the impact of basicity of different origins. Comparison of adsorption isotherms and adsorption distribution coefficients showed that the ammonia gas treatment was more effective than the high-temperature treatment in enhancing surface basicity. The resultant higher point of zero charges and total basicity (measured by total HCl uptake) correlated with improved adsorption affinity for PFOS and PFOA. The effectiveness of surface modification to enhance adsorption varied with carbon raw material. Wood-based carbons and activated carbon fibers showed enhancement by one to three orders of magnitudes while other materials could experience reduction in adsorption towards either PFOS or PFOA. PMID:26469934

  14. Non-aqueous formation of the calcium carbonate polymorph vaterite: astrophysical implications

    CERN Document Server

    Day, Sarah J; Parker, Julia E; Evans, Aneurin

    2013-01-01

    We study the formation of calcium carbonate, through the solid-gas interaction of amorphous Ca-silicate with gaseous CO2, at elevated pressures, and link this to the possible presence of calcium carbonate in a number of circumstellar and planetary environments. We use in-situ synchrotron X-Ray powder diffraction to obtain detailed structural data pertaining to the formation of the crystalline calcium carbonate phase vaterite and its evolution with temperature. We found that the metastable calcium carbonate phase vaterite was formed alongside calcite, at elevated CO2 pressure, at room temperature and subsequently remained stable over a large range of temperature and pressure. We report the formation of the calcium carbonate mineral vaterite whilst attempting to simulate carbonate dust grain formation in astrophysical environments. This suggests that vaterite could be a mineral component of carbonate dust and also presents a possible method of formation for vaterite and its polymorphs on planetary surfaces.

  15. Error analysis of equilibrium studies for the almond shell activated carbon adsorption of Cr(VI) from aqueous solutions

    International Nuclear Information System (INIS)

    In this study, the preparation of activated carbon from almond shell with H2SO4 activation and its ability to remove toxic hexavalent chromium from aqueous solutions are reported. The influences of several operating parameters such as pH, particle size and temperature on the adsorption capacity were investigated. Adsorption of Cr(VI) is found to be highly pH, particle size and temperature dependent. Four adsorption isotherm models namely, Langmuir, Freundlich, Tempkin and Dubinin-Radushkevich were used to analyze the equilibrium data. The Langmuir isotherm provided the best correlation for Cr(VI) onto the almond shell activated carbon (ASC). Adsorption capacity was calculated from the Langmuir isotherm as 190.3 mg/g at 323 K. Thermodynamic parameters were evaluated and the adsorption was endothermic showing monolayer adsorption of Cr(VI). Five error functions were used to treat the equilibrium data using non-linear optimization techniques for evaluating the fit of the isotherm equations. The highest correlation for the isotherm equations in this system was obtained for the Freundlich isotherm. ASC is found to be inexpensive and effective adsorbent for removal of Cr(VI) from aqueous solutions

  16. Sorption of mercury (II) and atrazine by biochar, modified biochars and biochar based activated carbon in aqueous solution.

    Science.gov (United States)

    Tan, Guangcai; Sun, Weiling; Xu, Yaru; Wang, Hongyuan; Xu, Nan

    2016-07-01

    Corn straw biochar (BC) was used as a precursor to produce Na2S modified biochar (BS), KOH modified biochar (BK) and activated carbon (AC). Experiments were conducted to compare the sorption capacity of these sorbents for aqueous Hg (II) and atrazine existed alone or as a mixture. In comparison to BC, the sorption capacity of BS, BK and AC for single Hg (II) increased by 76.95%, 32.12% and 41.72%, while that for atrazine increased by 38.66%, 46.39% and 47 times, respectively. When Hg (II) and atrazine coexisted in an aqueous solution, competitive sorption was observed on all these sorbents. Sulfur impregnation was an efficient way to enhance the Hg (II) removal due to the formation of HgS precipitate, and oxygen-containing functional groups on the sorbents also contributed to Hg (II) sorption. Activated carbon was the best sorbent for atrazine removal because of its extremely high specific surface area. PMID:27061260

  17. Artificial neural network approach for atomic coordinate prediction of carbon nanotubes

    Science.gov (United States)

    Acı, Mehmet; Avcı, Mutlu

    2016-07-01

    In this paper, four artificial neural network (ANN) models [i.e., feed-forward neural network (FFNN), function fitting neural network (FITNET), cascade-forward neural network (CFNN) and generalized regression neural network] have been developed for atomic coordinate prediction of carbon nanotubes (CNTs). The research reported in this study has two primary objectives: (1) to develop ANN prediction models that calculate atomic coordinates of CNTs instead of using any simulation software and (2) to use results of the ANN models as an initial value of atomic coordinates for reducing number of iterations in calculation process. The dataset consisting of 10,721 data samples was created by combining the atomic coordinates of elements and chiral vectors using BIOVIA Materials Studio CASTEP (CASTEP) software. All prediction models yield very low mean squared normalized error and mean absolute error rates. Multiple correlation coefficient (R) results of FITNET, FFNN and CFNN models are close to 1. Compared with CASTEP, calculation times decrease from days to minutes. It would seem possible to predict CNTs' atomic coordinates using ANN models can be successfully used instead of mathematical calculations.

  18. Influence of bicarbonate and carbonate ions on sonochemical degradation of Rhodamine B in aqueous phase.

    Science.gov (United States)

    Merouani, Slimane; Hamdaoui, Oualid; Saoudi, Fethi; Chiha, Mahdi; Pétrier, Christian

    2010-03-15

    The influence of bicarbonate and carbonate ions on sonolytic degradation of cationic dye, Rhodamine B (RhB), in water was investigated. As a consequence of ultrasonic cavitation that generates .OH radicals, carbonate radicals were secondary products of water sonochemistry when it contains dissolved bicarbonate or carbonate ions. The results clearly demonstrated the significant intensification of sonolytic destruction of RhB in the presence of bicarbonate and carbonate, especially at lower dye concentrations. Degradation intensification occurs because carbonate radicals sonochemically formed undergo radical-radical recombination at a lesser extent than hydroxyl radicals. The generated carbonate radicals are likely able to migrate far from the cavitation bubbles towards the solution bulk and are suitable for degradation of an organic dye such as RhB. Therefore, at low dye concentrations, carbonate radical presents a more selective reactivity towards RhB molecules than hydroxyl radical. In the presence of bicarbonate, degradation rate reached a maximum at 3 g L(-1) bicarbonate, but subsequent addition retards the destruction process. In RhB solutions containing carbonate, the oxidation rate gradually increased with increasing carbonate concentration up to 10 g L(-1) and slightly decreased afterward. Carbonate radicals sonochemically generated are suitable for total removal of COD of sonicated RhB solutions. PMID:19910116

  19. PREFACE: XXIX International Conference on Photonic, Electronic, and Atomic Collisions (ICPEAC2015)

    Science.gov (United States)

    Díaz, C.; Rabadán, I.; García, G.; Méndez, L.; Martín, F.

    2015-09-01

    The 29th International Conference on Photonic, Electronic and Atomic Collisions (XXIX ICPEAC) was held at the Palacio de Congresos ''El Greco'', Toledo, Spain, on 22-28 July, 2015, and was organized by the Universidad Autónoma de Madrid (UAM) and the Consejo Superior de Investigaciones Científicas (CSIC). ICPEAC is held biannually and is one of the most important international conferences on atomic and molecular physics. The topic of the conference covers the recent progresses in photonic, electronic, and atomic collisions with matter. With a history back to 1958, ICPEAC came to Spain in 2015 for the very first time. UAM and CSIC had been preparing the conference for six years, ever since the ICPEAC International General Committee made the decision to hold the XXIX ICPEAC in Toledo. The conference gathered 670 participants from 52 countries and attracted 854 contributed papers for presentation in poster sessions. Among the latter, 754 are presented in issues 2-12 of this volume of the Journal of Physics Conference Series. In addition, five plenary lectures, including the opening one by the Nobel laureate Prof. Ahmed H. Zewail and the lectures by Prof. Maciej Lewenstein, Prof. Paul Scheier, Prof. Philip H. Bucksbaum, and Prof. Stephen J. Buckman, 62 progress reports and 26 special reports were presented following the decision of the ICPEAC International General Committee. Detailed write-ups of most of the latter are presented in issue 1 of this volume, constituting a comprehensive tangible record of the meeting. On the occasion of the International Year of Light (IYL2015) and with the support of the Fundación Española para la Ciencia y la Tecnología (FECYT), the program was completed with two public lectures delivered by the Nobel laureate Prof. Serge Haroche and the Príncipe de Asturias laureate Prof. Pedro M. Echenique on, respectively, ''Fifty years of laser revolutions in physics'rquot; and ''The sublime usefulness of useless science''. Also a

  20. Bifunctional, Carbon-Free Nickel/Cobalt-Oxide Cathodes for Lithium-Air Batteries with an Aqueous Alkaline Electrolyte

    International Nuclear Information System (INIS)

    Highlights: • High activity bi-functional catalyst combination for ORR and OER . • An optimum ratio of high active bi-functional catalysts was found. • Novel electrodes without carbon to avoid carbon corrosion during OER mode. • EIS model for OER describes influence of a growing oxide layers. • Long-term test exhibited an excellent long-term stability over 1200 cycles. - Abstract: Lithium-air batteries with an aqueous alkaline electrolyte promise a very high practical energy density and capacity. These batteries are mainly limited by high overpotentials on the bifunctional cathode during charge and discharge. To reduce overpotentials the bifunctional cathode of such batteries must be improved significantly. Nickel is relatively inexpensive and has a good catalytic activity in alkaline media. Co3O4 was found to be a promising metal oxide catalyst for oxygen evolution in alkaline media but it has a low electronic conductivity. On the other hand since nickel has a good electronic conductivity Co3O4 can be added to pure nickel electrodes to enhance performance due to a synergetic effect. Due to the poor stability of carbon materials at high anodic potentials, gas diffusion electrodes were prepared without carbon to improve especially long-term stability. Gas diffusion electrodes were electrochemically investigated in a half cell. In addition, cyclic voltammogrametry (CV) and electrochemical impedance spectroscopy (EIS) were carried out. SEM was used for the physical and morphological investigations. Investigations showed that electrodes containing 20 wt.% Co3O4 exhibited the highest performance