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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. Copyright © 2016. Published by Elsevier B.V.

  2. Fe atom exchange between aqueous Fe2+ and magnetite.

    Science.gov (United States)

    Gorski, Christopher A; Handler, Robert M; Beard, Brian L; Pasakarnis, Timothy; Johnson, Clark M; Scherer, Michelle M

    2012-11-20

    The reaction between magnetite and aqueous Fe(2+) has been extensively studied due to its role in contaminant reduction, trace-metal sequestration, and microbial respiration. Previous work has demonstrated that the reaction of Fe(2+) with magnetite (Fe(3)O(4)) results in the structural incorporation of Fe(2+) and an increase in the bulk Fe(2+) content of magnetite. It is unclear, however, whether significant Fe atom exchange occurs between magnetite and aqueous Fe(2+), as has been observed for other Fe oxides. Here, we measured the extent of Fe atom exchange between aqueous Fe(2+) and magnetite by reacting isotopically "normal" magnetite with (57)Fe-enriched aqueous Fe(2+). The extent of Fe atom exchange between magnetite and aqueous Fe(2+) was significant (54-71%), and went well beyond the amount of Fe atoms found at the near surface. Mössbauer spectroscopy of magnetite reacted with (56)Fe(2+) indicate that no preferential exchange of octahedral or tetrahedral sites occurred. Exchange experiments conducted with Co-ferrite (Co(2+)Fe(2)(3+)O(4)) showed little impact of Co substitution on the rate or extent of atom exchange. Bulk electron conduction, as previously invoked to explain Fe atom exchange in goethite, is a possible mechanism, but if it is occurring, conduction does not appear to be the rate-limiting step. The lack of significant impact of Co substitution on the kinetics of Fe atom exchange, and the relatively high diffusion coefficients reported for magnetite suggest that for magnetite, unlike goethite, Fe atom diffusion is a plausible mechanism to explain the rapid rates of Fe atom exchange in magnetite.

  3. 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...

  4. Iron Atom Exchange between Hematite and Aqueous Fe(II).

    Science.gov (United States)

    Frierdich, Andrew J; Helgeson, Maria; Liu, Chengshuai; Wang, Chongmin; Rosso, Kevin M; Scherer, Michelle M

    2015-07-21

    Aqueous Fe(II) has been shown to exchange with structural Fe(III) in goethite without any significant phase transformation. It remains unclear, however, whether aqueous Fe(II) undergoes similar exchange reactions with structural Fe(III) in hematite, a ubiquitous iron oxide mineral. Here, we use an enriched (57)Fe tracer to show that aqueous Fe(II) exchanges with structural Fe(III) in hematite at room temperature, and that the amount of exchange is influenced by particle size, pH, and Fe(II) concentration. Reaction of 80 nm-hematite (27 m(2) g(-1)) with aqueous Fe(II) at pH 7.0 for 30 days results in ∼5% of its structural Fe(III) atoms exchanging with Fe(II) in solution, which equates to about one surface iron layer. Smaller, 50 nm-hematite particles (54 m(2) g(-1)) undergo about 25% exchange (∼3× surface iron) with aqueous Fe(II), demonstrating that structural Fe(III) in hematite is accessible to the fluid in the presence of Fe(II). The extent of exchange in hematite increases with pH up to 7.5 and then begins to decrease as the pH progresses to 8.0, likely due to surface site saturation by sorbed Fe(II). Similarly, when we vary the initial amount of added Fe(II), we observe decreasing amounts of exchange when aqueous Fe(II) is increased beyond surface saturation. This work shows that Fe(II) can catalyze iron atom exchange between bulk hematite and aqueous Fe(II), despite hematite being the most thermodynamically stable iron oxide.

  5. 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.

  6. Aqueous mercury adsorption by activated carbons.

    Science.gov (United States)

    Hadi, Pejman; To, Ming-Ho; Hui, Chi-Wai; Lin, Carol Sze Ki; McKay, Gordon

    2015-04-15

    Due to serious public health threats resulting from mercury pollution and its rapid distribution in our food chain through the contamination of water bodies, stringent regulations have been enacted on mercury-laden wastewater discharge. Activated carbons have been widely used in the removal of mercuric ions from aqueous effluents. The surface and textural characteristics of activated carbons are the two decisive factors in their efficiency in mercury removal from wastewater. Herein, the structural properties and binding affinity of mercuric ions from effluents have been presented. Also, specific attention has been directed to the effect of sulfur-containing functional moieties on enhancing the mercury adsorption. It has been demonstrated that surface area, pore size, pore size distribution and surface functional groups should collectively be taken into consideration in designing the optimal mercury removal process. Moreover, the mercury adsorption mechanism has been addressed using equilibrium adsorption isotherm, thermodynamic and kinetic studies. Further recommendations have been proposed with the aim of increasing the mercury removal efficiency using carbon activation processes with lower energy input, while achieving similar or even higher efficiencies. Copyright © 2015 Elsevier Ltd. All rights reserved.

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

    Science.gov (United States)

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

    2015-01-01

    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-[H2Nb6O19]6- has drastically different solution behaviour than lithium-[Nb6O19]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.

  8. Detection of gas atoms with carbon nanotubes

    Science.gov (United States)

    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. 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.

  9. Photochemical processing of aqueous atmospheric brown carbon

    Directory of Open Access Journals (Sweden)

    R. Zhao

    2015-06-01

    Full Text Available 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.

  10. 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.

  11. 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.

  12. Synthesized Magnetic Activated Carbon for Phosphate Removal from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Emad Dehghanifard

    2017-09-01

    Conclusion: The high efficacy of the adsorption process in this study showed that magnetic activated carbon had good capability in the removal of phosphate and can be used as an appropriate and new method for phosphate removal from aqueous solutions

  13. 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...

  14. Lead removal in aqueous solution by activated carbons prepared ...

    African Journals Online (AJOL)

    AJL

    and battery manufacturing, paint, paper and pulp industries. ... metals aqueous solutions is realizable using many methods such as: ion exchange, .... Table 1. Characteristics of the activated carbon. Activated carbons. Ash (%). Acidity neutralizations (meq/L). Surface area (m2/g). NaOH. NaHCO3. Na2CO3. CAo. 1.3. 0.8.

  15. Measurement of the inherent strength of carbon atomic chains

    Science.gov (United States)

    Mikhailovskij, I. M.; Sadanov, E. V.; Kotrechko, S.; Ksenofontov, V. A.; Mazilova, T. I.

    2013-01-01

    The intrinsic strength of freestanding carbon atomic chains was measured by in situ high-field mechanical testing of carbon atomic chains carried out inside a field-ion microscope. The determined breaking field strength corresponds to a tensile strength of carbon atomic chains at 5 K equal to 245 GPa. Carbon atomic chains also show exceptionally high-evaporation stability in electric fields up to 259 V/nm. The tensile strength of linear carbon chains significantly exceeds the tensile strength of known two-dimensional and three-dimensional carbon materials, including carbon nanotubes and graphene. Our results can be considered as direct experimental evidence for Pauling's prediction of bond stiffening with reduced atomic bond order.

  16. Atom exchange between aqueous Fe(II) and structural Fe in clay minerals.

    Science.gov (United States)

    Neumann, Anke; Wu, Lingling; Li, Weiqiang; Beard, Brian L; Johnson, Clark M; Rosso, Kevin M; Frierdich, Andrew J; Scherer, Michelle M

    2015-03-03

    Due to their stability toward reductive dissolution, Fe-bearing clay minerals are viewed as a renewable source of Fe redox activity in diverse environments. Recent findings of interfacial electron transfer between aqueous Fe(II) and structural Fe in clay minerals and electron conduction in octahedral sheets of nontronite, however, raise the question whether Fe interaction with clay minerals is more dynamic than previously thought. Here, we use an enriched isotope tracer approach to simultaneously trace Fe atom movement from the aqueous phase to the solid ((57)Fe) and from the solid into the aqueous phase ((56)Fe). Over 6 months, we observed a significant decrease in aqueous (57)Fe isotope fraction, with a fast initial decrease which slowed after 3 days and stabilized after about 50 days. For the aqueous (56)Fe isotope fraction, we observed a similar but opposite trend, indicating that Fe atom movement had occurred in both directions: from the aqueous phase into the solid and from the solid into aqueous phase. We calculated that 5-20% of structural Fe in clay minerals NAu-1, NAu-2, and SWa-1 exchanged with aqueous Fe(II), which significantly exceeds the Fe atom layer exposed directly to solution. Calculations based on electron-hopping rates in nontronite suggest that the bulk conduction mechanism previously demonstrated for hematite1 and suggested as an explanation for the significant Fe atom exchange observed in goethite2 may be a plausible mechanism for Fe atom exchange in Fe-bearing clay minerals. Our finding of 5-20% Fe atom exchange in clay minerals indicates that we need to rethink how Fe mobility affects the macroscopic properties of Fe-bearing phyllosilicates and its role in Fe biogeochemical cycling, as well as its use in a variety of engineered applications, such as landfill liners and nuclear repositories.

  17. 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.

  18. 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.

  19. Role of Surfactant Molecular Structure on Self Assembly: Aqueous SDBS on Carbon Nanotubes

    Science.gov (United States)

    Suttipong, Manaswee; Thompson, John R.; Tummala, Naga Rajesh; Kitiyanan, Boonyarach; Striolo, Alberto

    2011-03-01

    Stabilizing aqueous dispersions of carbon nanotubes mono-dispersed in diameter and chirality remains elusive. Surfactants have proven useful in deploying ultra-centrifugation techniques, but the molecular mechanism responsible for their effectiveness remains not fully understood. Based on a number of recent molecular simulation results, including those from our group, it appears that the morphology of the self-assembled surfactant aggregates on the carbon nanotubes strongly affects the effective potential of mean force between pairs of interacting carbon nanotubes. In this work we explore the effect of surfactant molecular structure on the properties of aqueous surfactant self-assembled aggregates. We employ equilibrium all-atom molecular dynamics simulations. We consider the surfactant SDBS (sodium dodecyl benzene sulfonate) with benzene ring located on the fifth or on the twelfth carbon atom in the tail, and the surfactant AOT [sodium bis(2-ethylhexyl) sulfosuccinate]. The simulations are conducted at room conditions for different surface coverages on (6,6), (12,12), and (20,20) single walled carbon nanotubes. These new results will help us identify the surfactant properties that allow us to manipulate nanotube-nanotube effective interactions. Research supported by the Department of Energy via CANTEC.

  20. Lead removal in aqueous solution by activated carbons prepared ...

    African Journals Online (AJOL)

    Three activated carbons prepared from vegetable matters of Gabonese biomass are being investigated as adsorbents for the removal of Pb (II) ions from aqueous solutions by means of batch technique. The equilibrium adsorption level was determined to be a function of pH, contact time, temperature and adsorbent dosage.

  1. Lead ions removal from aqueous solution using modified carbon ...

    Indian Academy of Sciences (India)

    33

    Abstract. Surface-modified carbon nanotubes (CNTs) were prepared in order to remove lead ions (Pb2+) from aqueous solution. The modification of CNTs was conducted by the oxidation, using the mixture of nitric acid (HNO3) and sulfuric acid (H2SO4). The adsorption behavior was well fitted to the Langmuir model and the ...

  2. Kinetics of absorption of carbon dioxide in aqueous ammonia solutions

    NARCIS (Netherlands)

    Derks, P. W. J.; Versteeg, G. F.

    2009-01-01

    In the present work the absorption of carbon dioxide into aqueous ammonia solutions has been studied in a stirred cell reactor, at low temperatures and ammonia concentrations ranging from 0.1 to about 7 kmol m-3. The absorption experiments were carried out at conditions where the so-called pseudo

  3. 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

  4. Kinetics of absorption of carbon dioxide in aqueous MDEA solutions with carbonic anhydrase at 298 K

    NARCIS (Netherlands)

    Penders-van Elk, Nathalie J. M. C.; Derks, Peter W. J.; Fradette, Sylvie; Versteeg, Geert F.

    In present work the absorption of carbon dioxide in aqueous N-methyldiethanolamine (MDEA) solutions with and without the enzyme carbonic anhydrase has been studied in a stirred cell at 298 K, with MDEA concentrations ranging from 0.5 to 4 kmol m(-3) and carbonic anhydrase concentrations ranging from

  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. Imaging the atomic orbitals of carbon atomic chains with field-emission electron microscopy

    Science.gov (United States)

    Mikhailovskij, I. M.; Sadanov, E. V.; Mazilova, T. I.; Ksenofontov, V. A.; Velicodnaja, O. A.

    2009-10-01

    A recently developed high-field technique of atomic chains preparation has made it possible to attain the ultrahigh resolution of field-emission electron microscopy (FEEM), which can be used to direct imaging the intra-atomic electronic structure. By applying cryogenic FEEM, we are able to resolve the spatial configuration of atomic orbitals, which correspond to quantized states of the end atom in free-standing carbon atomic chains. Knowledge of the intra-atomic structure will make it possible to visualize generic aspects of quantum mechanics and also lead to approaches for a wide range of nanotechnological applications.

  7. Atom Collision-Induced Resistivity of Carbon Nanotubes

    National Research Council Canada - National Science Library

    Hugo E. Romero; Kim Bolton; Arne Rosén; Peter C. Eklund

    2005-01-01

    We report the observation of unusually strong and systematic changes in the electron transport in metallic single-walled carbon nanotubes that are undergoing collisions with inert gas atoms or small molecules...

  8. Establishment of carbon atomic composition analysis by proton backscattering

    CERN Document Server

    Gotoh, Y; Fujii, R; Tsuji, H; Ishikawa, J

    2003-01-01

    Transition metal nitride and carbide thin films are expected to serve as a cathode material for cold cathodes. Since the atomic compositions of nitrogen and carbon will strongly affect the properties of the electron emission surface, quantification of these elements are necessary. In this report, we tried to quantify the carbon atomic compositions in the transition metal carbide thin films by resonant nuclear reaction of sup 1 sup 2 C(p, p) sup 1 sup 2 C.

  9. Covalent modification of single wall carbon nanotubes upon gamma irradiation in aqueous media

    Directory of Open Access Journals (Sweden)

    Jovanović Svetlana P.

    2011-01-01

    Full Text Available Single wall carbon nanotubes (SWCNTs were exposed to gamma radiation, absorbing the doses of 25, 50 and 100 kGy in aqueous environment. After the irradiation treatment, the changes in the structure were studied using Fourier Transform Infrared and Raman spectroscopy, thermogravimetric analysis and atomic force microscopy. Fourier Transform Infrared Spectroscopy has shown that the irradiation of SWCNTs in aqueous environment leads to covalent functionalization of SWCNTs. The irradiation of water leads to its radiolysis and the formation of free radical species of different types. These species react with nanotube sidewalls and in such way carboxylic and hydroxylic groups are covalently bonded to the sidewalls of SWCNTs. Thermogravimetric analysis was used to estimate the total amount of covalently bonded groups. The highest ratio of covalently bonded groups appears in nanotubes irradiated with the 100 kGy dose. Raman spectroscopy proves that the increase in irradiation doses leads to an increase of structural disorder of SWCNTs, presumably in the form of defects in carbon nanotube walls. Examination of ID to IG ratio shows a three times larger degree of structural disorder after the irradiation treatment with 100 kGy. The analysis of carbon nanotube Raman spectra RBM bands determined the presence of both semiconducting and metallic carbon nanotubes after gamma irradiation treatment. These measurements prove that gamma irradiation treatments have a nonselective effect regarding different chirality and therefore conductance of nanotubes. Atomic force microscopy shows a significant carbon nanotube shortening as the effect of gamma radiation treatment. Nanotubes with length between 500 nm and 1 μm are predominant.

  10. Aqueous Carbonation of Natural Brucite for CO2 Sequestration

    Science.gov (United States)

    Zhao, L.; Sang, L.; Chen, J.; Ji, J.; Teng, H.

    2009-12-01

    Experimental study is carried out at conditions of room temperature and moderate CO2 pressure to examine the carbonation reaction of natural brucite in aqueous environment. Two sets of initial conditions are examined, one is brucite in pure water, and the other is in 1% HCl. Time-dependent XRD analysis shows that carbon fixation process begins within 30 min of the experiments irrespective of the original makeup of the slurry. Ensuing measurements by XRD and FT-IR reveal that nesquehonite (> 78%) is by far the dominant C-bearing species in the carbonate mineral product assembly. Minor product components observed in water are basic magnesium carbonate hydromagnesite and dypingite; when HCl is added in the starting slurry, chloride-bearing artinite replaces hydromagnesite. However, thermodynamic calculation suggests that the assembly of such composition is most likely a kinetically favored product at the experimental conditions which are more strongly saturated with respect to hydromagnesite and magnesite than to nesquehonite. A pseudo first-order rate law is found to best describe the time-dependent measurements for both water and HCl experiments. Moreover, fitting the rate expression to the experimental data yields a higher rate constant for the experiments performed in HCl solutions. The faster kinetics relative to that in water implies that the carbonation reaction may be a multi-stepped process, involving first the dissolution of brucite and CO2 to generate Mg2+ and CO32-, followed by precipitation of magnesium carbonate phases from aqueous solutions. This leads to our proposition that direct heterogeneous reaction between hydrated CO2 and solid phase of Mg(OH)2 is probably not the pathway for the overall carbonation process. Assuming the upper limit of carbon content Cmax = 8.7% (based upon that of nesquehonite), measured total carbon in the product Ctot show a carbonation rate of 83.9% and 94.3% for brucite in HCl and DDW at the end of 2.5 hr experiments

  11. Small angle neutron and X-ray studies of carbon structures with metal atoms

    Science.gov (United States)

    Lebedev, V. T.; Szhogina, A. A.; Bairamukov, V. Yu

    2017-05-01

    Encapsulation of metal atoms inside carbon single-wall cages or within multi-layer cells has been realized using molecular precursors and high temperature processes transforming them into desirable structures. Endohedral fullerenols Fe@C60(OH)X with 3d-metal (iron) have been studied by SANS in aqueous solutions where they form stable globular clusters with radii R C ∼ 10-12 nm and aggregation numbers N C ∼ 104. This self-assembly is a crucial feature of paramagnetic fullerenols as perspective contrast agents for Magneto-Resonance Imaging in medicine. Cellular carbon-metal structures have been created by the pyrolysis of diphthalocyanines of lanthanides and actinides. It was established that these ultra porous matrices consist of globular cells of molecular precursor size (∼ 1 nm) which are aggregated into superstructures. This provides retain of metal atoms inside matrices which may serve for safety storage of spent fuel of nuclear power plants.

  12. International atomic time and time transfer

    Science.gov (United States)

    Lewandowski, Wlodzimierz

    Global Navigation Satellite Systems (GNSS) keep a central role in the international timekeeping. American Global Positioning System (GPS) is a navigation system that has proven itself to be a reliable source of positioning for both the military community and the civilian community. But, little known by many, is the fact that GPS has proven itself to be an important and valuabe utility to the timekeeping community (Lewandowski et al. 1999). GPS is a versatile and global tool which can be used to both distribute time to an arbitrary number of users and synchronise clocks over large distances with a high degree of precision and accuracy. Similar performance can be obtained with Russian Global Navigation Satellite System (GLONASS). It is expected in the near future satellites of a new European navigation system GALILEO might bring some important opportunities for international timekeeping. This paper after a brief introduction to international timekeeping focuses on the description of recent progress in time transfer techniques using GNSS satellites.

  13. Theoretical isotopic fractionation between structural boron in carbonates and aqueous boric acid and borate ion

    Science.gov (United States)

    Balan, Etienne; Noireaux, Johanna; Mavromatis, Vasileios; Saldi, Giuseppe D.; Montouillout, Valérie; Blanchard, Marc; Pietrucci, Fabio; Gervais, Christel; Rustad, James R.; Schott, Jacques; Gaillardet, Jérôme

    2018-02-01

    The 11B/10B ratio in calcite and aragonite is an important proxy of oceanic water pH. However, the physico-chemical mechanisms underpinning this approach are still poorly known. In the present study, we theoretically determine the equilibrium isotopic fractionation properties of structural boron species in calcium carbonates, BO33-, BO2(OH)2- and B(OH)4- anions substituted for carbonate groups, as well as those of B(OH)4- and B(OH)3 species in vacuum. Significant variability of equilibrium isotopic fractionation properties is observed among these structural species which is related to their contrasted coordination state, Bsbnd O bond lengths and atomic-scale environment. The isotopic composition of structural boron does not only depend on its coordination number but also on its medium range environment, i.e. farther than its first coordination shell. The isotopic fractionation between aqueous species and their counterparts in vacuum are assessed using previous investigations based on similar quantum-mechanical modeling approaches. At 300 K, the equilibrium isotope composition of structural trigonal species is 7-15‰ lighter than that of aqueous boric acid molecules, whereas substituted tetrahedral borate ions are heavier than their aqueous counterparts by 10-13‰. Although significant uncertainties are known to affect the theoretical prediction of fractionation factors between solids and solutions, the usually assumed lack of isotopic fractionation during borate incorporation in carbonates is challenged by these theoretical results. The present theoretical equilibrium fractionation factors between structural boron and aqueous species differ from those inferred from experiments which may indicate that isotopic equilibrium, unlike chemical equilibrium, was not reached in most experiments. Further research into the isotopic fractionation processes at the interface between calcium carbonates and aqueous solution as well as long duration experiments aimed at

  14. THE INTERNATIONAL ATOMIC ENERGY AGENCY’s SAFEGUARDS SYSTEM

    OpenAIRE

    Eugenio-Andrés, Gabriel; Universidad Católica de Cordoba

    2008-01-01

    Entrusted with the responsibility of establishing and administering the international safeguards system with the purpose of ensuring that nuclear energy would not be used for furthering military purposes, the International Atomic Energy Agency (hereinafter “IAEA” or “the Agency”) is a key piece of the international system for the maintenance of world peace and security. Despite the initial enthusiasm surrounding the foundation of the IAEA in the 1950s, it required several years for the Agency...

  15. 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.

  16. Differential determination of selenium(IV) and selenium(VI) with sodium diethyldithiocarbamate, ammonium pyrrolidinedithiocarbamate and dithizone by atomic-absorption spectrophotometry with a carbon-tube atomizer.

    Science.gov (United States)

    Kamada, T; Shiraishi, T; Yamamoto, Y

    1978-01-01

    The extraction behaviour of selenium(IV) and selenium(VI) with sodium diethyldithiocarbamate, ammonium pyrrolidinedithiocarbamate and dithizone in organic solvents has been investigated by means of flameless atomic-absorption spectrophotometry with a carbon-tube atomizer. The selective extraction of selenium(IV) and differential determination of selenium(IV) and selenium(VI) have been developed. With sodium diethyldithiocarbamate and carbon tetrachloride, when the aqueous phase/organic solvent volume ratio is 5 and the injection volume in the carbon tube is 20 microl, the sensitivity for selenium is 0.4 ng/ml for 1% absorption. The relative standard deviations are ca. 3%. Interference by many metal ions can he prevented by masking with EDTA. The proposed methods have been applied satisfactorily to determination of Se(IV) and Se(VI) in various types of water.

  17. Atomic carbon in an infrared dark cloud

    NARCIS (Netherlands)

    Ossenkopf, Volker; Ormel, Chris W.; Simon, Robert; Sun, Kefeng; Stutzki, Jürgen

    2010-01-01

    Infrared dark clouds (IRDCs) are potential sites of massive star formation, dark in the near-infrared, but in many cases already with indications of active star-formation from far-infrared and submm observations. They are an ideal test bed to study the role of internal and external heating on the

  18. Multi-instrumental characterization of carbon nanotubes dispersed in aqueous solutions

    Science.gov (United States)

    Previous studies showed that the dispersion extent and physicochemical properties of carbon nanotubes are highly dependent upon the preparation methods (e.g., dispersion methods and dispersants). In the present work, multiwalled carbon nanotubes (MWNTs) are dispersed in aqueous s...

  19. Observation of liposomes of differing lipid composition in aqueous medium by means of atomic force microscopy.

    Science.gov (United States)

    Takechi-Haraya, Yuki; Sakai-Kato, Kumiko; Abe, Yasuhiro; Kawanishi, Toru; Okuda, Haruhiro; Goda, Yukihiro

    2016-08-01

    Liposomes present a challenge for atomic force microscopy (AFM) observation in aqueous medium because they easily collapse. Here, we demonstrate that bovine serum albumin coating of a glass substrate enables AFM observation of various liposomes in aqueous medium. With this AFM system, liposomes can be systematically observed and morphologically analyzed regardless of their surface charge, phase state, degree of lipid acyl chain unsaturation or PEG modification. This system thus has the potential to reveal the mechanical properties of liposomes of various lipid types and contents. © The Author 2016. Published by Oxford University Press on behalf of The Japanese Society of Microscopy. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

  20. 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.

  1. Note: A microfluidic freezer based on evaporative cooling of atomized aqueous microdroplets.

    Science.gov (United States)

    Song, Jin; Chung, Minsub; Kim, Dohyun

    2015-01-01

    We report for the first time water-based evaporative cooling integrated into a microfluidic chip for temperature control and freezing of biological solution. We opt for water as a nontoxic, effective refrigerant. Aqueous solutions are atomized in our device and evaporation of microdroplets under vacuum removes heat effectively. We achieve rapid cooling (-5.1 °C/s) and a low freezing temperature (-14.1 °C). Using this approach, we demonstrate freezing of deionized water and protein solution. Our simple, yet effective cooling device may improve many microfluidic applications currently relying on external power-hungry instruments for cooling and freezing.

  2. Dielectric barrier discharge carbon atomic emission spectrometer: universal GC detector for volatile carbon-containing compounds.

    Science.gov (United States)

    Han, Bingjun; Jiang, Xiaoming; Hou, Xiandeng; Zheng, Chengbin

    2014-01-07

    It was found that carbon atomic emission can be excited in low temperature dielectric barrier discharge (DBD), and an atmospheric pressure, low power consumption, and compact microplasma carbon atomic emission spectrometer (AES) was constructed and used as a universal and sensitive gas chromatographic (GC) detector for detection of volatile carbon-containing compounds. A concentric DBD device was housed in a heating box to increase the plasma operation temperature to 300 °C to intensify carbon atomic emission at 193.0 nm. Carbon-containing compounds directly injected or eluted from GC can be decomposed, atomized, and excited in this heated DBD for carbon atomic emission. The performance of this new optical detector was first evaluated by determination of a series of volatile carbon-containing compounds including formaldehyde, ethyl acetate, methanol, ethanol, 1-propanol, 1-butanol, and 1-pentanol, and absolute limits of detection (LODs) were found at a range of 0.12-0.28 ng under the optimized conditions. Preliminary experimental results showed that it provided slightly higher LODs than those obtained by GC with a flame ionization detector (FID). Furthermore, it is a new universal GC detector for volatile carbon-containing compounds that even includes those compounds which are difficult to detect by FID, such as HCHO, CO, and CO2. Meanwhile, hydrogen gas used in conventional techniques was eliminated; and molecular optical emission detection can also be performed with this GC detector for multichannel analysis to improve resolution of overlapped chromatographic peaks of complex mixtures.

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

    Science.gov (United States)

    Yu, Jin-Gang; Zhao, Xiu-Hui; Yang, Hua; Chen, Xiao-Hong; Yang, Qiaoqin; Yu, Lin-Yan; Jiang, Jian-Hui; Chen, Xiao-Qing

    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. Copyright © 2014 Elsevier B.V. All rights reserved.

  4. 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.)

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

    National Research Council Canada - National Science Library

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

    2016-01-01

    ... 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...

  6. 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.

  7. International carbon trade with constrained allowance choices

    NARCIS (Netherlands)

    Yu, S.; Weikard, H.P.; Zhu, X.; Ierland, van E.C.

    2017-01-01

    International carbon markets are advocated in order to involve more countries in an agreement for the mitigation of greenhouse gas emissions and to reduce the costs of mitigation. In this paper we develop a model where allowances are endogenously determined by each member of a carbon trade

  8. 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.

  9. 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

  10. Heat conduction in double-walled carbon nanotubes with intertube additional carbon atoms.

    Science.gov (United States)

    Cui, Liu; Feng, Yanhui; Tan, Peng; Zhang, Xinxin

    2015-07-07

    Heat conduction of double-walled carbon nanotubes (DWCNTs) with intertube additional carbon atoms was investigated for the first time using a molecular dynamics method. By analyzing the phonon vibrational density of states (VDOS), we revealed that the intertube additional atoms weak the heat conduction along the tube axis. Moreover, the phonon participation ratio (PR) demonstrates that the heat transfer in DWCNTs is dominated by low frequency modes. The added atoms cause the mode weight factor (MWF) of the outer tube to decrease and that of the inner tube to increase, which implies a lower thermal conductivity. The effects of temperature, tube length, and the number and distribution of added atoms were studied. Furthermore, an orthogonal array testing strategy was designed to identify the most important structural factor. It is indicated that the tendencies of thermal conductivity of DWCNTs with added atoms change with temperature and length are similar to bare ones. In addition, thermal conductivity decreases with the increasing number of added atoms, more evidently for atom addition concentrated at some cross-sections rather than uniform addition along the tube length. Simultaneously, the number of added atoms at each cross-section has a considerably more remarkable impact, compared to the tube length and the density of chosen cross-sections to add atoms.

  11. Stability of conductance oscillations in carbon atomic chains

    Science.gov (United States)

    Yu, Jing-Xin; Hou, Zhi-Wei; Liu, Xiu-Ying

    2015-06-01

    The conductance stabilities of carbon atomic chains (CACs) with different lengths are investigated by performing theoretical calculations using the nonequilibrium Green’s function method combined with density functional theory. Regular even-odd conductance oscillation is observed as a function of the wire length. This oscillation is influenced delicately by changes in the end carbon or sulfur atoms as well as variations in coupling strength between the chain and leads. The lowest unoccupied molecular orbital in odd-numbered chains is the main transmission channel, whereas the conductance remains relatively small for even-numbered chains and a significant drift in the highest occupied molecular orbital resonance toward higher energies is observed as the number of carbon atoms increases. The amplitude of the conductance oscillation is predicted to be relatively stable based on a thiol joint between the chain and leads. Results show that the current-voltage evolution of CACs can be affected by the chain length. The differential and second derivatives of the conductance are also provided. Project supported by the National Natural Science Foundation of China (Grant Nos. 11304079, 11404094, and 51201059), the Priority Scientific and Technological Project of Henan Province, China (Grant No. 14A140027), the School Fund (Grant No. 2012BS055), and the Plan of Natural Science Fundamental Research of Henan University of Technology, China (Grant No. 2014JCYJ15).

  12. Making non-aqueous high internal phase pickering emulsions: influence of added polymer and selective drying.

    Science.gov (United States)

    Cai, Dongyu; Thijssen, Job H T; Clegg, Paul S

    2014-06-25

    We report the first example of a non-aqueous (oil-in-oil) Pickering high internal phase emulsion (HIPE) stabilized by chemically modified fumed silica. In this case, a 75 vol % ethylene carbonate (EC)-rich internal phase is emulsified in 25 vol % p-xylene (xylene)-rich continuous phase using interfacial nanoparticles. It is revealed that no phase inversion takes place during the HIPE formation process when using the appropriate wettability of solid particles. Incorporating polystyrene (PS) into xylene enables one-step formation of PS-filled HIPEs in place of a multi-step polymerization of the continuous phase. We observe that the size of droplets changes with the addition of PS, and we associate this with the change in the viscosity of the continuous xylene-rich phase. Drying the pure HIPE results in the selective removal of xylene and coalescence of EC-rich droplets. With the PS in the xylene-rich continuous phase, we show that EC-rich droplets can be retained even though the xylene is evaporated off, and a new semi-solid composite containing both liquid phase and solid phase is formed via this non-aqueous Pickering-HIPE template.

  13. Ordering of carbon atoms in boron carbide structure

    Energy Technology Data Exchange (ETDEWEB)

    Ponomarev, V. I., E-mail: i2212@yandex.ru; Kovalev, I. D.; Konovalikhin, S. V.; Vershinnikov, V. I. [Russian Academy of Sciences, Institute of Structural Macrokinetics and Materials Science (Russian Federation)

    2013-05-15

    Boron carbide crystals have been obtained in the entire compositional range according to the phase diagram by self-propagating high-temperature synthesis (SHS). Based on the results of X-ray diffraction investigations, the samples were characterized by the unit-cell metric and reflection half-width in the entire range of carbon concentrations. A significant spread in the boron carbide unit-cell parameters for the same carbon content is found in the data in the literature; this spread contradicts the structural concepts for covalent compounds. The SHS samples have not revealed any significant spread in the unit-cell parameters. Structural analysis suggests that the spread of parameters in the literary data is related to the unique process of ordering of carbon atoms in the boron carbide structure.

  14. 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.

  15. International Atomic Energy Agency (IAEA) and the Diplomacy of Sustainable International Nuclear Security

    OpenAIRE

    Martin Uadiale

    2011-01-01

    The increasing threat and proliferation of Nuclear Weapons and materials across national and international boundaries have combined to pose severe threat to the stability of the international system. In this respect, the International Atomic Energy Agency (IAEA) has through its robust activities helped to enthrone the virtues of sustainable Nuclear security in our fast, but ever-changing world. This study concluded the IAEA, regardless of its numerous short comings, have proved to be an all i...

  16. Aqueous stabilisation of carbon-encapsulated superparamagnetic α-iron nanoparticles for biomedical applications.

    Science.gov (United States)

    Aguiló-Aguayo, Noemí; Maurizi, Lionel; Galmarini, Sandra; Ollivier-Beuzelin, Marie Gabrielle; Coullerez, Géraldine; Bertran, Enric; Hofmann, Heinrich

    2014-09-28

    Carbon-based nanomaterials, such as carbon-encapsulated magnetic nanoparticles (CEMNP, core@shell), show a wide range of desirable properties for applications in the biomedical field (clinical MRI, hyperthermia), for energy production and storage (hydrogen storage), for the improvement of electronic components and for environmental applications (water-treatment). However, this kind of nanoparticle tends to aggregate in water suspensions. This often hampers the processability of the suspensions and presents an obstacle to their application in many fields. Here the stabilisation of core-shell Fe-C nanoparticles by surface adsorbed polyvinyl-alcohol (PVA) is presented. Different PVA/CEMNP mass ratios (9, 36, 144 and 576 w/w) were studied. Several characterisation techniques were used in order to determine the size distribution of the particles and to optimize the PVA/CEMNP ratio. A good colloidal stability was obtained for spherical nanoparticles about 50 nm in diameter containing several superparamagnetic Fe cores. The nanoparticles were found to be isolated and well dispersed in solution. The use of PVA for coating carbon-encapsulated Fe nanoparticles does not only result in a good colloidal stability in aqueous suspensions, but the resulting particles also show low cytotoxicity and an interesting cell internalization behaviour. The simple stabilization method developed here can likely be extended to other core@shell nanoparticle systems as well as other carbon-based nanomaterials in the future.

  17. Current-induced dynamics in carbon atomic contacts

    DEFF Research Database (Denmark)

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

    2011-01-01

    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......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...... 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...

  18. 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

  19. Manipulation and soldering of carbon nanotubes using atomic force microscope

    Science.gov (United States)

    Kashiwase, Yuta; Ikeda, Takayuki; Oya, Takahide; Ogino, Toshio

    2008-09-01

    Manipulation of carbon nanotubes (CNTs) by an atomic force microscope (AFM) and soldering of CNTs using Fe oxide nanoparticles are described. We succeeded to separate a CNT bundle into two CNTs or CNT bundles, to move the separated CNT to a desirable position, and to bind it to another bundle. For the accurate manipulation, load of the AFM cantilever and frequency of the scan were carefully selected. We soldered two CNTs using an Fe oxide nanoparticle prepared from a ferritin molecule. The adhesion forces between the soldered CNTs were examined by an AFM and it was found that the CNTs were bound, though the binding force was not strong.

  20. A New Mixed All-Atom/Coarse-Grained Model: Application to Melittin Aggregation in Aqueous Solution.

    Science.gov (United States)

    Shelley, Mee Y; Selvan, Myvizhi Esai; Zhao, Jun; Babin, Volodymyr; Liao, Chenyi; Li, Jianing; Shelley, John C

    2017-08-08

    We introduce a new mixed resolution, all-atom/coarse-grained approach (AACG), for modeling peptides in aqueous solution and apply it to characterizing the aggregation of melittin. All of the atoms in peptidic components are represented, while a single site is used for each water molecule. With the full flexibility of the peptide retained, our AACG method achieves speedups by a factor of 3-4 for CPU time reduction and another factor of roughly 7 for diffusion. An Ewald treatment permits the inclusion of long-range electrostatic interactions. These characteristics fit well with the requirements for studying peptide association and aggregation, where the system sizes and time scales require considerable computational resources with all-atom models. In particular, AACG is well suited for biologics since changes in peptide shape and long-range electrostatics may play an important role. The application of AACG to melittin, a 26-residue peptide with a well-known propensity to aggregate in solution, serves as an initial demonstration of this technology for studying peptide aggregation. We observed the formation of melittin aggregates during our simulations and characterized the time-evolution of aggregate size distribution, buried surface areas, and residue contacts. Key interactions including π-cation and π-stacking involving TRP19 were also examined. Our AACG simulations demonstrated a clear salt effect and a moderate temperature effect on aggregation and support the molten globule model of melittin aggregates. As a showcase, this work illustrates the useful role for AACG in investigations of peptide aggregation and its potential to guide formulation and design of biologics.

  1. Calcite growth rates as a function of aqueous calcium-to-carbonate ratio, saturation index and strontium concentration

    Energy Technology Data Exchange (ETDEWEB)

    Bracco, Jacquelyn N [ORNL; Grantham, Ms. Meg [Georgia Institute of Technology; Stack, Andrew G [ORNL

    2012-01-01

    Using in situ atomic force microscopy, the growth rates of the obtuse and acute step orientations on the calcite surface were measured at two saturation indices as a function of the aqueous calcium-to-carbonate ratio and aqueous strontium concentration. The amount of strontium required to inhibit growth was found to correlate with the aqueous calcium concentration, but did not correlate with carbonate. This suggests that strontium inhibits attachment of calcium ions to the reactive sites on the calcite surface. Strontium/calcium cation exchange selectivity coefficients for those sites, Kex, of 1.09 0.09 and 1.44 0.19 are estimated for the obtuse and acute step orientations, respectively. The implication of this finding is that to avoid poisoning calcite growth, the concentration of calcium should be higher than the quotient of the strontium concentration and Kex, regardless of saturation state. Additionally, analytical models of nucleation and propagation of steps are expanded from previous work to capture growth rates of these steps at multiple saturation indices and the effect of strontium. This work will have broader implications for naturally occurring or engineered calcite growth, such as to sequester subsurface strontium contamination.

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

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yingfeng [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China Electric Power University, Beijing, 102206 (China); Li, Meicheng, E-mail: mcli@ncepu.edu.cn [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China Electric Power University, Beijing, 102206 (China); Su Zhou Institute, North China Electric Power University, Suzhou, 215123 (China); Gu, TianSheng [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China Electric Power University, Beijing, 102206 (China); Bai, Fan [School of Materials Science and Engineering, Harbin Institute of Technology, Harbin, 150001 (China); Yu, Yue; Trevor, Mwenya [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China Electric Power University, Beijing, 102206 (China); Yu, Yangxin [Department of Chemical Engineering, Tsinghua University, Beijing, 100084 (China)

    2013-11-01

    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.

  3. 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.

  4. The absorption of gases in aqueous activated carbon slurries enhanced by adsorbing or catalytic particles

    NARCIS (Netherlands)

    Holstvoogd, R.D.; van Swaaij, Willibrordus Petrus Maria; van Dierendonck, L.L.

    1988-01-01

    The enhanced absorption of gases in aqueous activated carbon slurries of fine particles is studied with an instationary absorption model taking into account the finite adsorption capacity of the carbon particles, and with a stationary geometrical model, which describes the absorption into a highly

  5. 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...

  6. Aqueous processing of DNA-dispersed carbon nanotubes

    Science.gov (United States)

    Khripin, Constantine

    Single-walled carbon nanotubes (CNTs) are a promising material for many nanoscale electronic applications. CNTs are able to carry very high currents, and are very sensitive to the environment around them making them ideal for sensing on a very small scale. However, to date no significant commercial applications have been achieved because of difficulties in sorting the nanotubes by type, placing them on a target site and interfacing them into a device such as a field-effect transistor (FET) that could be used as a sensor. CNTs are well dispersed in water by DNA, and form a stable hybrid structure, DNA-CNT. This hybrid can be sorted according to CNT length and chirality using Ion-Exchange Chromatography (IEC), providing a valuable route to CNT purification. This thesis centers on helping explain how the purification process works and on developing ways to place the DNA-CNT from an aqueous suspension on a target site to be used in a device. Purification is done by IEC, which separates species partly on the basis of their electrostatic properties in solution. ABAQUS(TM) finite-element models of DNA-CNT electrostatics are reported which help explain, for example, how metallic CNTs screen the charge on DNA more than semiconducting ones. Other applications of Poison-Boltzmann solution electrostatics theory, including the electrostatic field near a metal electrode, are also reported. Understanding electrostatic fields near an electrode plays a role in dielectrophoretic placement of CNTs. Experimental results are reported on Meniscus Alignment, a way of placing and orienting DNA-CNT on top of a self-assembled monolayer (SAM) and kinetics models are developed to help explain the process. Meniscus Alignment is shown to be a versatile technique which can produce finely tuned deposition densities and spatially varying alignment patterns. Finally, a Capillary Electrophoresis (CE) study of the DNA-CNT is reported. This study found that CE has some capacity for sorting DNA-CNT by

  7. 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.

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

    Science.gov (United States)

    Warren, K. M.; Mpagazehe, J. N.; LeDuc, P. R.; Higgs, C. F.

    2014-10-01

    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.

  9. 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.

  10. Synthesis of novel size exclusion chromatography support by surface initiated aqueous atom transfer radical polymerization.

    Science.gov (United States)

    Coad, Bryan R; Kizhakkedathu, Jayachandran N; Haynes, Charles A; Brooks, Donald E

    2007-11-06

    We report the use of aqueous surface-initiated atom transfer radical polymerization (SI-ATRP) to grow polymer brushes from a "gigaporous" polymeric chromatography support for use as a novel size exclusion chromatography medium. Poly(N,N-dimethylacrylamide) (PDMA) was grown from hydrolyzable surface initiators via SI-ATRP catalyzed by 1,1,4,7,10,10-hexamethyltriethylenetetramine (HMTETA)/CuCl. Grafted polymer was characterized semiquantitatively by ATR-FTIR and also cleaved and quantitatively characterized for mass, molecular weight, and polydispersity via analytical SEC/MALLS. The synthesis provides control over graft density and allows the creation of dense brushes. Incorporation of negative surface charge was found to be crucial for improving the initiation efficiency. As polymer molecular weight and density could be controlled through reaction conditions, the resulting low-polydispersity grafted polymer brush medium is shown to be suitable for use as a customizable size exclusion chromatography medium for investigating the principals of entropic interaction chromatography. All packed media investigated showed size-dependent partitioning of solutes, even for low graft density systems. Increasing the molecular weight of the grafts allowed solutes more access to the volume fraction in the column available for partitioning. Compared to low graft density media, increased graft density caused eluted solute probes to be retained less within the column and allowed for greater size discrimination of probes whose molecular weights were less than 10(4) kDa.

  11. Comparison studies of surface cleaning methods for PAN-based carbon fibers with acetone, supercritical acetone and subcritical alkali aqueous solutions

    Science.gov (United States)

    Meng, Linghui; Fan, Dapeng; Huang, Yudong; Jiang, Zaixing; Zhang, Chunhua

    2012-11-01

    Four kinds of polyacrylonitrile-based carbon fibers were cleaned by three methods and were characterized by X-ray photoelectron spectroscopy, monofilament tensile strength test and atomic force microscopy (AFM). Experimental results of these tests reveal that the method using supercritical acetone or subcritical potassium hydroxide aqueous solution act as the processing medium shows a better cleaning effect compared to the traditional method, Soxhlet extraction with acetone. The method using supercritical acetone is more appropriate to wipe off the oxygenated contaminants on carbon fibers' surfaces and causes a relatively smaller damage to the bulk strength of each carbon fiber. As far as treating method using the subcritical alkali aqueous solution, it can thoroughly remove silicious contaminants on the surfaces of treated fibers.

  12. Proposal for the International Atomic Energy Agency Training Course

    Energy Technology Data Exchange (ETDEWEB)

    McCarthy, T.L.

    1994-06-01

    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.

  13. 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

  14. The Relativistic Effects on the Carbon-Carbon Coupling Constants Mediated by a Heavy Atom.

    Science.gov (United States)

    Wodyński, Artur; Malkina, Olga L; Pecul, Magdalena

    2016-07-21

    The (2)JCC, (3)JCC, and (4)JCC spin-spin coupling constants in the systems with a heavy atom (Cd, In, Sn, Sb, Te, Hg, Tl, Pb, Bi, and Po) in the coupling path have been calculated by means of density functional theory. The main goal was to estimate the relativistic effects on spin-spin coupling constants and to explore the factors which may influence them, including the nature of the heavy atom and carbon hybridization. The methods applied range, in order of reduced complexity, from the Dirac-Kohn-Sham (DKS) method (density functional theory with four-component Dirac-Coulomb Hamiltonian), through DFT with two- and one-component zeroth-order regular approximation (ZORA) Hamiltonians, to scalar effective core potentials (ECPs) with the nonrelativistic Hamiltonian. The use of DKS and ZORA methods leads to very similar results, and small-core ECPs of the MDF and MWB variety reproduce correctly the scalar relativistic effects. Scalar relativistic effects usually are larger than the spin-orbit coupling effects. The latter tend to influence the most the coupling constants of the sp(3)-hybridized carbon atoms and in compounds of the p-block heavy atoms. Large spin-orbit coupling contributions for the Po compounds are probably connected with the inverse of the lowest triplet excitation energy.

  15. Relation Between the Adsorbed Quantity and the Immersion Enthalpy in Catechol Aqueous Solutions on Activated Carbons

    Science.gov (United States)

    Moreno-Piraján, Juan Carlos; Blanco, Diego; Giraldo, Liliana

    2012-01-01

    An activated carbon, CarbochemTM—PS230, was modified by chemical and thermal treatment in flow of H2, in order to evaluate the influence of the activated carbon chemical characteristics in the adsorption of the catechol. The catechol adsorption in aqueous solution was studied along with the effect of the pH solution in the adsorption process of modified activated carbons and the variation of immersion enthalpy of activated carbons in the aqueous solutions of catechol. The interaction solid-solution is characterized by adsorption isotherms analysis, at 298 K and pH 7, 9 and 11 in order to evaluate the adsorption value above and below that of the catechol pKa. The adsorption capacity of carbons increases when the solution pH decreases. The retained amount increases slightly in the reduced carbon to maximum adsorption pH and diminishes in the oxidized carbon. Similar conclusions are obtained from the immersion enthalpies, whose values increase with the solute quantity retained. In granular activated carbon (CAG), the immersion enthalpies obtained are between 21.5 and 45.7 J·g−1 for catechol aqueous solutions in a range of 20 at 1500 mg·L−1. PMID:22312237

  16. PREFACE: XXVIth International Conference on Photonic, Electronic and Atomic Collisions

    Science.gov (United States)

    Orel, Ann; Starace, Anthony F.; Nikolić, Dragan; Berrah, Nora; Gorczyca, Thomas W.; Kamber, Emanuel Y.; Tanis, John A.

    2009-12-01

    The XXVIth International Conference on Photonic, Electronic and Atomic Collisions was held on the campus of Western Michigan University (WMU) in Kalamazoo during 22-28 July 2009. Kalamazoo, the home of a major state university amid pleasant surroundings, was a delightful place for the conference. The 473 scientific participants, 111 of whom were students, had many fruitful discussions and exchanges that contributed to the success of the conference. Participants from 43 countries made the conference truly international in scope. The 590 abstracts that were presented on the first four days formed the heart of the conference and provided ample opportunity for discussion. This change, allowing the conference to end with invited talks, was a departure from the format used at previous ICPEAC gatherings in which the conferences ended with a poster session. The abstracts were split almost equally between the three main conference areas, i.e., photonic, electronic, and atomic collisions, and the posters were distributed across the days of the conference so that approximately equal numbers of abstracts in the different areas were scheduled for each day. Of the total number of presented abstracts, 517 of these are included in this proceedings volume, the first time that abstracts have been published by ICPEAC. There were 5 plenary lectures covering the different areas of the conference: Paul Corkum (University of Ottawa) talked on attosecond physics with atoms and molecules, Serge Haroche (Collège de France) on non-destructive photon counting, Toshiyuki Azuma (Tokyo Metropolitan University) on resonant coherent excitation of highly-charged ions in crystals, Eva Lindroth (Stockholm University) on atomic structure effects, and Alfred Müller (Justus Liebig University) on resonance phenomena in electron- and photon-ion collisions. Two speakers gave very illuminating public lectures that drew many people from the local area, as well as conference participants: Patricia Dehmer

  17. In situ ellipsometry study of atomic hydrogen etching of extreme ultraviolet induced carbon layers

    NARCIS (Netherlands)

    Chen, J. Q.; E. Louis,; Harmsen, R.; T. Tsarfati,; Wormeester, H.; van Kampen, M.; van Schaik, W.; van de Kruijs, R.; F. Bijkerk,

    2011-01-01

    Atomic hydrogen based etching is generally considered an efficient method for the removal of carbon films resulting from photo-induced hydrocarbon dissociation, as occurs in extreme ultraviolet (EUV) photolithography environments. The etch rate of atomic hydrogen for three different kinds of carbon

  18. 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.

  19. Lead ions removal from aqueous solution using modified carbon ...

    Indian Academy of Sciences (India)

    2018-02-02

    Feb 2, 2018 ... Pb2+ was a spontaneous and endothermic process. The ion exchange mechanism of Pb2+ removal was confirmed by the pH and electrical conductivity data in solution before and after adsorption. Keywords. Carbon nanotubes; surface modification; lead ions removal; surface-modified carbon nanotubes.

  20. 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.

  1. Combined Effect of Temperature and pKa on the Kinetics of Absorption of Carbon Dioxide in Aqueous Alkanolamine and Carbonate Solutions with Carbonic Anhydrase

    NARCIS (Netherlands)

    Penders-Van Elk, Nathalie J M C; Oversteegen, S. Martijn; Versteeg, Geert F.

    2016-01-01

    In present work the absorption of carbon dioxide in aqueous N-methyldiethanolamine, N,N-dimethylethanolamine, and triisopropanolamine solutions with and without the enzyme carbonic anhydrase has been studied in a stirred cell reactor at temperatures varying between 278 and 313 K, at an alkanolamine

  2. 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...

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

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Jian [State Key Laboratory of Marine Environmental Science, College of the Environment and Ecology, Xiamen University, Xiamen 361102 (China); Department of Chemistry and Biochemistry, University of Texas, 700 Planetarium Place, Arlington, TX 76019 (United States); Sengupta, Mrinal K. [Department of Chemistry and Biochemistry, University of Texas, 700 Planetarium Place, Arlington, TX 76019 (United States); Thermo Fisher Scientific, Dionex Products, 445 Lakeside Drive, Sunnyvale, CA, 94085 (United States); Yuan, Dongxing [State Key Laboratory of Marine Environmental Science, College of the Environment and Ecology, Xiamen University, Xiamen 361102 (China); Dasgupta, Purnendu K., E-mail: Dasgupta@uta.edu [Department of Chemistry and Biochemistry, University of Texas, 700 Planetarium Place, Arlington, TX 76019 (United States)

    2014-06-01

    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

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

    Science.gov (United States)

    Zope, Rajendra R; Bhusal, Shusil; Basurto, Luis; Baruah, Tunna; Jackson, Koblar

    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 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.

  5. 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.

  6. Pulling platinum atomic chains by carbon monoxide molecules.

    Science.gov (United States)

    Makk, P; Balogh, Z; Csonka, Sz; Halbritter, A

    2012-08-07

    The interaction of carbon monoxide molecules with atomic-scale platinum nanojunctions is investigated by low temperature mechanically controllable break junction experiments. Combining plateau length analysis, two-dimensional conductance-displacement histograms and conditional correlation analysis a comprehensive microscopic picture is proposed about the formation and evolution of Pt-CO-Pt single-molecule configurations. Our analysis implies that before pure Pt monoatomic chains are formed a CO molecule infiltrates the junction, first in a configuration that is perpendicular to the contact axis. This molecular junction is strong enough to pull a monoatomic platinum chain with the molecule being incorporated in the chain. Along the chain formation the molecule can either stay in the perpendicular configuration, or rotate to a parallel configuration. The evolution of the single-molecule configurations along the junction displacement shows quantitative agreement with theoretical predictions, justifying the interpretation in terms of perpendicular and parallel molecular alignment. Our analysis demonstrates that the combination of two-dimensional conductance-displacement histograms with conditional correlation analysis is a useful tool to analyze separately fundamentally different types of junction trajectories in single molecule break junction experiments.

  7. True atomic-scale imaging of a spinel Li{sub 4}Ti{sub 5}O{sub 12}(111) surface in aqueous solution by frequency-modulation atomic force microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kitta, Mitsunori, E-mail: m-kitta@aist.go.jp; Kohyama, Masanori [Research Institute for Ubiquitous Energy Devices, National Institute of Advanced Industrial Science and Technology, 1-8-31 Midorigaoka, Ikeda, Osaka 563-8577 (Japan); Onishi, Hiroshi [Department of Chemistry, Graduate School of Science, Kobe University 1-1 Rokkodai, Nada, Kobe 657-8501 (Japan)

    2014-09-15

    Spinel-type lithium titanium oxide (LTO; Li{sub 4}Ti{sub 5}O{sub 12}) is a negative electrode material for lithium-ion batteries. Revealing the atomic-scale surface structure of LTO in liquid is highly necessary to investigate its surface properties in practical environments. Here, we reveal an atomic-scale image of the LTO(111) surface in LiCl aqueous solution using frequency-modulation atomic force microscopy. Atomically flat terraces and single steps having heights of multiples of 0.5 nm were observed in the aqueous solution. Hexagonal bright spots separated by 0.6 nm were also observed on the flat terrace part, corresponding to the atomistic contrast observed in the ultrahigh vacuum condition, which suggests that the basic atomic structure of the LTO(111) surface is retained without dramatic reconstruction even in the aqueous solution.

  8. The leachability of carbon-14-labelled 3,4-benzopyrene from coal ash into aqueous systems

    NARCIS (Netherlands)

    Besemer, A.C.; Kanij, J.

    1984-01-01

    The leachability of polycyclic aromatic hydrocarbons from coal ash into aqueous systems was studied. Carbon-14-labeled 3,4-Benzopyrene (BaP) was deposited on coal fly ash by adsorption from the liquid phase in quantities of about 10 ??g/g ash. After a thermal treatment in air at 120??C for 2 hours

  9. THE ENHANCEMENT OF THE PHYSICAL ABSORPTION OF GASES IN AQUEOUS ACTIVATED CARBON SLURRIES

    NARCIS (Netherlands)

    TINGE, JT; DRINKENBURG, AAH

    The enhancement of the gas-liquid mass transfer rates in aqueous slurries containing small activated carbon particles was studied in a semi-batchwise operated stirred cell absorber with a plane interface. The maximum observed enhancement factors for absorption of propane, ethene and hydrogen in the

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

    DEFF Research Database (Denmark)

    Paul, Subham; Thomsen, Kaj

    2012-01-01

    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...

  11. A calculation of internal kinetic energy and polarizability of compressed argon from the statistical atom model

    NARCIS (Netherlands)

    Seldam, C.A. ten; Groot, S.R. de

    1952-01-01

    From Jensen's and Gombás' modification of the statistical Thomas-Fermi atom model, a theory for compressed atoms is developed by changing the boundary conditions. Internal kinetic energy and polarizability of argon are calculated as functions of pressure. At 1000 atm. an internal kinetic energy of

  12. 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

  13. Sorption of lead from aqueous solution by modified activated carbon ...

    African Journals Online (AJOL)

    The present study aims to develop a simple and rapid procedure for lead (II) removal. Laboratory-scale adsorption experiments were conducted aiming to remove lead from water samples. They were based on using powdered activated carbon (PACI), which was prepared from olive stones generated, as plant wastes, and ...

  14. Comparison studies of surface cleaning methods for PAN-based carbon fibers with acetone, supercritical acetone and subcritical alkali aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Meng Linghui; Fan Dapeng [School of Chemical Engineering and Technology, Harbin Institute of Technology, P.O. Box 410, Harbin 150001 (China); Huang Yudong, E-mail: ydhuang.hit1@yahoo.com.cn [School of Chemical Engineering and Technology, Harbin Institute of Technology, P.O. Box 410, Harbin 150001 (China); Jiang Zaixing; Zhang Chunhua [School of Chemical Engineering and Technology, Harbin Institute of Technology, P.O. Box 410, Harbin 150001 (China)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer Cleaning with supercritical acetone is appropriate to wipe off the oxygenated contaminants. Black-Right-Pointing-Pointer Cleaning with supercritical acetone causes smaller damage to bulk strength of carbon fibers. Black-Right-Pointing-Pointer Cleaning with subcritical alkali aqueous solution can thoroughly remove silicious contaminants. - Abstract: Four kinds of polyacrylonitrile-based carbon fibers were cleaned by three methods and were characterized by X-ray photoelectron spectroscopy, monofilament tensile strength test and atomic force microscopy (AFM). Experimental results of these tests reveal that the method using supercritical acetone or subcritical potassium hydroxide aqueous solution act as the processing medium shows a better cleaning effect compared to the traditional method, Soxhlet extraction with acetone. The method using supercritical acetone is more appropriate to wipe off the oxygenated contaminants on carbon fibers' surfaces and causes a relatively smaller damage to the bulk strength of each carbon fiber. As far as treating method using the subcritical alkali aqueous solution, it can thoroughly remove silicious contaminants on the surfaces of treated fibers.

  15. GREEN SYNTHESIS OF CALCIUM AND PHOSPHATE COMPOUNDS BY VARYING pH VALUE AND Ca/P ATOMIC RATIO USING AQUEOUS PRECIPITATIONS

    Directory of Open Access Journals (Sweden)

    WEN CHENG CHEN

    2013-03-01

    Full Text Available Using an aqueous synthesis with varying pH values and changing ion source of calcium-to-phosphorus atomic ratios to clarify precipitations was the purpose of this study. The precipitation procedures were processed in two ways; firstly, a pH range of 3.0 to 12.0 was controlled while the ion source of relative Ca/P ratio was kept at 2.0. Secondly, the reaction was kept alkaline with a pH of 12.0 and the value range of Ca/P ratios in the precursor ion-solutions was 1.0 to 3.0. The physicochemical properties were measured to characterize the various precipitates. Results showed that when the pH was varied, the morphology of the precipitates gradually changed to micrometer column-like shape under acidic condition and nano-scale globular-like shape in alkaline environments. By controlling the pH and Ca/P ratio of ion-sources in aqueous reactions, precipitates in biphasics of calcium carbonate/apatite and calcium hydroxide/apatite were obtained with nanometer-scale morphologies. The precipitation procedures that are used in the synthesis of the biphasics provide a simpler, safer, less expensive and more environmentally friendly than the co-precipitation by sintering processes.

  16. Experimental fractionation of stable carbon isotopes during degassing of carbon dioxide and precipitation of calcite from aqueous solutions

    Science.gov (United States)

    Müller, K.; Winde, V.; Escher, P.; von Geldern, R.; Böttcher, M. E.

    2012-04-01

    Processes in the carbonate system of surface waters are in particular sensitive to variations of boundary conditions as, for instance, the partial pressure of carbon dioxide in the atmosphere and the aqueous solution. Examples range from streams, rivers, to coastal marine waters. The flux of carbon dioxide from continental flowing waters was recently included into calculations of the global carbon budget (Butman & Raymond, 2011, Nature Geo.). These solutions, are often supersaturated in carbon dioxide with respect to the atmosphere. The degassing of carbon dioxide is associated with a kinetically controlled fractionation of the stable carbon isotopes, which has to be considered in balancing water-air carbon dioxide fluxes. The degassing process additionally leads to the super-saturation of the aqueous solution with respect to calcium carbonate. Stable isotope fractionation is of particular value to identify and quantify processes at the water-gas phase interface and link these non-equilibrium processes to the formation mechanisms of calcite and the hydrodynamics of surface waters. Experiments were carried out with or without inert N2 gas flow to degas carbon dioxide from initially supersaturated solutions. Natural solutions used are from different stations of the Elbe estuary, the Jade Bay, the backbarrier tidal area of Spiekeroog Island, carbonate springs of Rügen Island, and the Baltic Sea coastline. Results are compared experiments using bottled mineral waters. By following the (physico) chemical changes in the solutions (pH, TA, Ca PHREEQC modeling) it was found, that two evolutionary stages can be differentiated. Reaction progress led to the preferential liberation of carbon dioxide containing the light carbon isotope, following a Rayleigh-type process. After an induction period, where only degassing of carbon dioxide took place, a second stage was observed where calcite began to form from the highly supersaturated solutions. In this stage the carbonate

  17. Characterization and Catalytic Upgrading of Aqueous Stream Carbon from Catalytic Fast Pyrolysis of Biomass

    Energy Technology Data Exchange (ETDEWEB)

    Starace, Anne K. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Black, Brenna A. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Lee, David D. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Palmiotti, Elizabeth C. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Orton, Kellene A. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Michener, William E. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; ten Dam, Jeroen [Johnson Matthey Technology Centre, P.O. Box 1, Belasis Avenue, Billingham, Cleveland TS23 1LB, United Kingdom; Watson, Michael J. [Johnson Matthey Technology Centre, P.O. Box 1, Belasis Avenue, Billingham, Cleveland TS23 1LB, United Kingdom; Beckham, Gregg T. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Magrini, Kimberly A. [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Mukarakate, Calvin [National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States

    2017-11-01

    Catalytic fast pyrolysis (CFP) of biomass produces a liquid product consisting of organic and aqueous streams. The organic stream is typically slated for hydrotreating to produce hydrocarbon biofuels, while the aqueous stream is considered a waste stream, resulting in the loss of residual biogenic carbon. Here, we report the detailed characterization and catalytic conversion of a CFP wastewater stream with the ultimate aim to improve overall biomass utilization within a thermochemical biorefinery. An aqueous stream derived from CFP of beech wood was comprehensively characterized, quantifying 53 organic compounds to a total of 17% organics. The most abundant classes of compounds are acids, aldehydes, and alcohols. The most abundant components identified in the aqueous stream were C1-C2 organics, comprising 6.40% acetic acid, 2.16% methanol, and 1.84% formaldehyde on wet basis. The CFP aqueous stream was catalytically upgraded to olefins and aromatic hydrocarbons using a Ga/HZSM-5 catalyst at 500 degrees C. When the conversion yield of the upgraded products was measured with fresh, active catalyst, 33% of the carbon in the aqueous stream was recovered as aromatic hydrocarbons and 29% as olefins. The majority of the experiments were conducted using a molecular beam mass spectrometer and separate GC-MS/FID experiments were used to confirm the assignments and quantification of products with fresh excess catalyst. The recovered 62% carbon in the form of olefins and aromatics can be used to make coproducts and/or fuels potentially improving biorefinery economics and sustainability. Spent catalysts were collected after exposure to varying amounts of the feed, and were characterized using multipoint-Brunauer-Emmett-Teller (BET) adsorption, ammonia temperature programmed desorption (TPD), and thermogravimetric analysis (TGA) to monitor deactivation of Ga/HZSM-5. These characterization data revealed that deactivation was caused by coke deposits, which blocked access to active

  18. Morphology and internal structure of polymeric and carbon nanofibers

    Science.gov (United States)

    Zhong, Zhenxin

    Evaporation and the associated solidification are important factors that affect the diameter of electrospun nanofibers. The evaporation and solidification of a charged jet were controlled by varying the partial pressure of water vapor during electrospinning of poly(ethylene oxide) from aqueous solution. As the partial pressure of water vapor increases, the solidification process of the charged jet becomes slower, allowing elongation of the charged jet to continue longer and thereby to form thinner fibers. The morphology and internal structure of electrospun poly(vinylidene fluorides) nanofibers were investigated. Low voltage high resolution scanning electron microscopy was used to study the surface of electrospun nanofibers. Control of electrospinning process produced fibers with various morphological forms. Fibers that were beaded, branched, or split were obtained when different instabilities dominated in the electrospinning process. The high ratio of stretching during electrospinning aligns the polymer molecules along the fiber axis. A rapid evaporation of solvent during electrospinning gives fibers with small and imperfect crystallites. These can be perfected by thermal annealing. Fibers annealed at elevated temperature form plate-like lamellar crystals tightly linked by tie molecules. Electrospinning can provide ultrafine nanofibers with cross-sections that contain only a few polymer molecules. Ultrafine polymer nanofibers are extremely stable in transmission electron microscope. Electrospun nanofibers suspended on a holey carbon film showed features of individual polymer molecules. Carbon fibers with diameters ranging from 100 nm to several microns were produced from mesophase pitch by a low cost gas jet process. The structure of mesophase pitch-based carbon fibers was investigated as a function of heat treatment temperatures. Submicron-sized graphene oxide flakes were prepared by a combination of oxidative treatment and ultrasonic radiation. Because pitch is

  19. A first principles study on the CVD graphene growth on copper surfaces: A carbon atom incorporation to graphene edges

    Science.gov (United States)

    Tajima, Nobuo; Kaneko, Tomoaki; Nara, Jun; Ohno, Takahisa

    2016-11-01

    Carbon atom reactions in the chemical vapor deposition (CVD) processes for graphene production on copper surfaces have been studied by first principles molecular dynamics (MD) simulations at a typical CVD growth temperature. This study focuses on the processes of a carbon atom incorporation to graphene edges. The energy barriers of these carbon atom incorporation reactions have been calculated as ~ 1 eV, which are comparable or slightly larger than the barriers of carbon atom dimerization. We have also found that the surface copper atoms form step like structures to terminate the carbon dangling bonds at graphene edges, which are markedly different from the graphene-copper interactions observed in static calculations.

  20. Energy and economic considerations for ex-situ and aqueous mineral carbonation

    Energy Technology Data Exchange (ETDEWEB)

    O' Connor, William K.; Dahlin, David C.; Rush, G.E.; Gerdemann, Stephen J.; Penner, L.R.

    2004-01-01

    Due to the scale and breadth of carbon dioxide emissions, and speculation regarding their impact on global climate, sequestration of some portion of these emissions has been under increased study. A practical approach to carbon sequestration will likely include several options, which will be driven largely by the energy demand and economics of operation. Aqueous mineral carbonation of calcium and magnesium silicate minerals has been studied as one potential method to sequester carbon dioxide. Although these carbonation reactions are all thermodynamically favored, they occur at geologic rates of reaction. Laboratory studies have demonstrated that these rates of reaction are accelerated with increasing temperature, pressure, and particle surface area. Mineral-specific activation methods were identified, however, each of these techniques incurs energy as well as economic costs. An overview of the mineral availability, pretreatment options and energy demands, and process economics is provided.

  1. Removal and Adsorption of p-Nitrophenol from Aqueous Solutions Using Carbon Nanotubes and Their Composites

    Directory of Open Access Journals (Sweden)

    Yuan-Xiang Yao

    2014-01-01

    Full Text Available In an attempt to explore the possibility of using carbon nanotubes (CNTs as efficient adsorbents for removal of pollutants from the contaminated water, the adsorption of p-nitrophenol (PNP on raw multiwalled carbon nanotubes (r.MWNTs with different outer diameters, various functionalized multiwalled carbon nanotubes (f-MWNTs, raw single-walled carbon nanotubes (r.SWNTs and oxidized single-walled carbon nanotubes (ox-SWNTs has been investigated. The ox-SWNTs showed better adsorption ability for PNP with different concentrations, while lower uptake capacity was found for all of the r.MWNTs and f-MWNTs. The removal efficiency of PNP by ox-SWNTs was around 98%, indicating that ox-SWNTs possess a great potential application prospect for removing PNP from aqueous solutions.

  2. Quantitative Atomic Force Microscopy with Carbon Monoxide Terminated Tips

    NARCIS (Netherlands)

    Sun, Zhixiang|info:eu-repo/dai/nl/314075674; Boneschanscher, Mark P.; Swart, Ingmar|info:eu-repo/dai/nl/304837652; Vanmaekelbergh, Daniel|info:eu-repo/dai/nl/304829137; Liljeroth, Peter|info:eu-repo/dai/nl/314007423

    2011-01-01

    Noncontact atomic force microscopy (AFM) has recently progressed tremendously in achieving atomic resolution imaging through the use of small oscillation amplitudes and well-defined modification of the tip apex. In particular, it has been shown that picking up simple inorganic molecules (such as CO)

  3. Application of Activated Carbon for Removal of Arsenic Ions from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    R. Ansari

    2007-01-01

    Full Text Available The activated carbon (AC was used for removal of As(III and As(V ions from aqueous solutions. Sorption experiments were conducted using both batch and column systems. The effect of some important parameters on sorption of these by AC was studied. It was found that among the different factors affecting sorption capacity and efficiency in removal of arsenic from aqueous solutions, the effect of pH and the oxidation state were the most prominent. The optimum pH values for removal of As(III and As(V from aqueous solutions using AC was found 12 and 3 respectively. Impregnation of AC with sulphur contain organic dyes, it is possible to improve As(III uptake considerably.

  4. Atmospheric plasma generates oxygen atoms as oxidizing species in aqueous solutions

    Czech Academy of Sciences Publication Activity Database

    Hefny, M.M.; Pattyn, C.; Lukeš, Petr; Benedikt, J.

    2016-01-01

    Roč. 49, č. 40 (2016), s. 404002 ISSN 0022-3727 R&D Projects: GA MŠk(CZ) LD14080 Grant - others:European Cooperation in Science and Technology(XE) COST TD1208 Institutional support: RVO:61389021 Keywords : atmospheric pressure plasma * transport of reactive species * reactive oxygen species * aqueous phase chemistry * plasma and liquids * phenol aqueous chemistry Subject RIV: BL - Plasma and Gas Discharge Physics Impact factor: 2.588, year: 2016 http://iopscience.iop.org/article/10.1088/0022-3727/49/40/404002

  5. 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.

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

    Science.gov (United States)

    Cong, Chunxiao; Li, Kun; Zhang, Xi Xiang; Yu, Ting

    2013-01-01

    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. PMID:23378926

  7. A carbonate-silicate aqueous geochemical cycle model for Mars

    Science.gov (United States)

    Schaefer, M. W.; Leidecker, H.

    1992-01-01

    A model for the carbonate-silicate geochemical cycle of an early, wet Mars is under development. The results of this study will be used to constrain models of the geochemical history of Mars and the likely mineralogy of its present surface. Although Mars today is a cold, dry planet, it may once have been much warmer and wetter. Values of total outgassed CO2 from several to about 10 bars are consistent with present knowledge (Pollack et al. 1987), and this amount of CO2 implies an amount of water outgassed at least equal to an equivalent depth of 500-1000 meters (Carr 1986). Pollack et al. (1987), in addition, estimate that a thick CO2 atmosphere may have existed for an extended period of time, perhaps as long as a billion years. The greenhouse effect of such an atmosphere would permit the presence of liquid water on the surface, most likely in the form of a shallow sea in the lowest regions of the planet, such as the northern plains (Schaefer 1990). The treatment of geochemical cycles as complex kinetic chemical reactions has been undertaken for terrestrial systems in recent years with much success (Lasaga 1980, 1981; Berner et al. 1983; Lasaga et al. 1985). Although the Martian system is vastly less well understood, and hence less well-constrained, it is also a much simpler system, due to the lack of biogenic reactions that make the terrestrial system so complex. It should be possible, therefore, to use the same techniques to model the Martian system as have been used for terrestrial systems, and to produce useful results. A diagram of the carbonate-silicate cycle for Mars (simplified from the terrestrial system) is given.

  8. Bulk and Surface Aqueous Speciation of Calcite: Implications for Low-Salinity Waterflooding of Carbonate Reservoirs

    KAUST Repository

    Yutkin, Maxim P.

    2017-08-25

    Low-salinity waterflooding (LSW) is ineffective when reservoir rock is strongly water-wet or when crude oil is not asphaltenic. Success of LSW relies heavily on the ability of injected brine to alter surface chemistry of reservoir crude-oil brine/rock (COBR) interfaces. Implementation of LSW in carbonate reservoirs is especially challenging because of high reservoir-brine salinity and, more importantly, because of high reactivity of the rock minerals. Both features complicate understanding of the COBR surface chemistries pertinent to successful LSW. Here, we tackle the complex physicochemical processes in chemically active carbonates flooded with diluted brine that is saturated with atmospheric carbon dioxide (CO2) and possibly supplemented with additional ionic species, such as sulfates or phosphates. When waterflooding carbonate reservoirs, rock equilibrates with the injected brine over short distances. Injected-brine ion speciation is shifted substantially in the presence of reactive carbonate rock. Our new calculations demonstrate that rock-equilibrated aqueous pH is slightly alkaline quite independent of injected-brine pH. We establish, for the first time, that CO2 content of a carbonate reservoir, originating from CO2-rich crude oil and gas, plays a dominant role in setting aqueous pH and rock-surface speciation. A simple ion-complexing model predicts the calcite-surface charge as a function of composition of reservoir brine. The surface charge of calcite may be positive or negative, depending on speciation of reservoir brine in contact with the calcite. There is no single point of zero charge; all dissolved aqueous species are charge determining. Rock-equilibrated aqueous composition controls the calcite-surface ion-exchange behavior, not the injected-brine composition. At high ionic strength, the electrical double layer collapses and is no longer diffuse. All surface charges are located directly in the inner and outer Helmholtz planes. Our evaluation of

  9. Internal polarized deuterium target with cryogenic atomic beam source

    CERN Document Server

    Dyug, M V; Lazarenko, B A; Mishnev, S I; Nikolenko, D M; Rachek, Igor A; Shestakov, Yu V; Sadykov, R S; Toporkov, D K; Zevakov, S A; Osipov, A V; Stibunov, V N

    2002-01-01

    Description of the polarized deuterium gas target used at the VEPP-3 electron storage ring for experiments on elastic and inelastic ed scattering is given. Superconducting sextupole magnets with the pole tip magnetic field up to 4.8 T are used in atomic beam source (ABS) to focus atoms. The flux of polarized atoms injected into the storage cell was measured to be 8.2x10 sup 1 sup 6 at/s for deuterium and 7.9x10 sup 1 sup 6 at/s for hydrogen. The measured target thickness 8x10 sup 1 sup 3 at/cm sup 2 is consistent with the thickness calculated from the measured beam intensity. The effective tensor polarization of the deuterium target during the experiment was found to be P sub z sub z =0.397. Further improvements of the target and possible limitation of the beam intensity from ABS are discussed.

  10. Functionalized carbon nanotubes based filters for chromium removal from aqueous solutions.

    Science.gov (United States)

    Elsehly, Emad M; Chechenin, N G; Makunin, A V; Motaweh, H A; Leksina, E G

    2017-04-01

    This investigation examines the filtration efficiency of chromium from aqueous solution using two types of commercial multiwalled carbon nanotubes (MWCNTs) (Taunit-M (TM) and Taunit-MD (TMD)). These MWCNTs were modified using two complementary treatments, purification (using a mixture of hydrochloric acid and hydrogen peroxide) and functionalization (using nitric acid). The effect of these treatments on the morphology of MWCNT Taunit filters was characterized by scanning electron microscopy and energy dispersive X-ray spectroscopy to estimate the outer diameter distribution and element content deposited on filters. Effects of different parameters, i.e., carbon nanotube filter mass, concentration of chromium in aqueous solution, and pH of aqueous solution, on removal of this heavy metal were determined. From these investigations, the removal efficiency of chromium could reach 97% for modified TM and 70% for modified TMD at concentration of 10 ppm, suggesting that modified TM is an excellent adsorbent for chromium removal from aqueous solutions and more efficient than modified TMD. A significant increase in chromium removal by modified TM at pH = 2 has been observed compared with higher pH values. It was found that modified TM filters can be reused through many cycles of regeneration with high performance. Modified TM filters may be a promising candidate for heavy metal ion removal from industrial wastewater.

  11. Sodium carbonate as phase promoter in aqueous solutions of imidazolium and pyridinium ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Deive, Francisco J. [Chemical Engineering Department, University of Santiago de Compostela, E-15782 Santiago de Compostela (Spain); Rivas, Miguel A. [Applied Physics Department, University of Vigo, 36310 Vigo (Spain); Rodriguez, Ana, E-mail: aroguez@uvigo.es [Chemical Engineering Department, University of Vigo, 36310 Vigo (Spain)

    2011-08-15

    Highlights: > The discovery of novel aqueous two-phase systems, exclusively formed by the mixture of an ionic liquid and sodium carbonate is presented. > We explore for the first time the ability of pyridinium-based ionic liquids to form aqueous biphasic systems. > A first advance of the benefits of using benzylimidazolium-based ionic liquids for aqueous two-phase systems is proposed. - Abstract: Several methylsulfate and chloride anion-based ionic liquids, such as 1-alkyl-3-methyl imidazolium methyl sulfate, C{sub n}MIM CH{sub 3}SO{sub 4} (n = 1, 2, and 4), 1-benzyl-3-methyl imidazolium methyl sulfate, BzMIM CH{sub 3}SO{sub 4}, 1-benzyl, or hexyl-3-methyl imidazolium chloride, XMIM Cl (X = Bz and Hx), and methylpyridinium methylsulfate, Mpy CH{sub 3}SO{sub 4}, with sodium carbonate, Na{sub 2}CO{sub 3}, as phase forming salt, have been investigated and discussed for their potential use in separations based on aqueous two-phase systems (ATPS). Phase diagrams have been experimentally ascertained at T = 298.15 K, and Merchuck equation and a variation of this model have been used for correlating the binodal data. The alkyl chain length in the cation and the type of anion and cation have been explored and discussed due to their decisive influence in the ATPS behavior. The consistence of tie-line data was ascertained by applying the Othmer-Tobias and Bancroft equations.

  12. The removal of metallic single-walled carbon nanotubes using an aqueous two-phase system.

    Science.gov (United States)

    Tang, Malcolm S Y; Whitcher, T J; Yeoh, K H; Chua, C L; Woon, K L; Show, P L; Lin, Y K; Ling, T C

    2014-05-01

    Here we report our findings on the removal of metallic single-walled carbon nanotubes using an aqueous two-phase system. The aqueous two-phase system contained as received carbon nanotubes, polyethylene glycol, dextran, N-methylpyrrolidone, cetyltrimethylammonium bromide, and water which phase separated into top and bottom phases. The top phase was dominated by polyethylene glycol whereas the bottom phase was dominated by dextran. The dextran-rich phase contained more semiconducting species while metallic species was more abundant in the polyethylene glycol rich-phase. It was found via Fourier-Transform Infrared Spectroscopy that cetyltrimethylammonium bromide only present in the dextran-rich phase. A selectivity mechanism is tentatively proposed and discussed.

  13. The Study of Oxidized Multi-Walled Carbon Nanotubes Efficiency in Lead Removing from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    M Malakootian

    2015-07-01

    Full Text Available Introduction: Carbon nano tubes are products which have the ability to remove some contaminants from aqueous solutions and wastewater. The efficiency of these products depends on different factors such as PH, concentration, contact, mixing time, etc. in this research the efficiency of oxidized multi- walled carbon nanotubes is studied. Methods: The study is Experimental. The multi-walled carbon nanotubes were oxidized and Three PH 4, 7 and 10 and contact times 5, 10 and 40 min, and the concentrations of 50, 100 and 125 mg of carbon nanotubes from aqueous Pb removal efficiency were examined.All of the tests were done according to the standard methods for the examination of water and wastewater book 21th edited..Real samples of drinking water was the village of Ebrahim Abad RazaviSirjan. Data analysis was done using SPSS statistical software version 16 Results: By Simultaneous changes in time and PH was changed the efficiency of lead removal by the oxidized multi- walled carbon nanotubes. The most important factor in increasing the efficiency of removal, using acidic PH (PH =4 is. With a Simultaneous increase in contact time and concentration of nanotubes, the removal efficiency increased. In optimal conditions, 125 mg of nanotube concentration, contact time of 10 minutes and PH=4 removal of lead in synthetic samples and real samples, respectively, 99.1 and 94% were achieved. In total there is little difference between the real conditions and the synthetic conditions of the removal efficiency that this difference arises from the interaction of cations, anions and heavy metals in real samples. Conclusion: Oxidized multi-walled Carbon nanotubes has a high capacity for the removal of lead from aqueous solutions.

  14. Bromate removal from aqueous solutions by ordered mesoporous carbon.

    Science.gov (United States)

    Xu, Chunhua; Wang, Xiaohong; Shi, Xiaolei; Lin, Sheng; Zhu, Liujia; Che, Yaming

    2014-01-01

    We investigated the feasibility of using ordered mesoporous carbon (OMC) for bromate removal from water. Batch experiments were performed to study the influence of various experimental parameters such as the effect of contact time, adsorbent dosage, initial bromate concentration, temperature, pH and effect of competing anions on bromate removal by OMC. The adsorption kinetics indicates that the uptake rate ofbromate was rapid at the beginning: 85% adsorption was completed in 1 h and equilibrium was achieved within 3 h. The sorption process was well described with pseudo-second-order kinetics. The maximum adsorption capacity of OMC for bromate removal was 17.6 mg g(-1) at 298 K. The adsorption data fit the Freundlich model well. The amount of bromate removed was found to be proportional to the influent bromate concentration. The effects of competing anions and solution pH (3-11) were negligible. These limited data suggest that OMC can be effectively utilized for bromate removal from drinking water.

  15. Lipid-carbon nanotube self-assembly in aqueous solution.

    Science.gov (United States)

    Qiao, Rui; Ke, Pu Chun

    2006-10-25

    One major drawback associated with single-walled carbon nanotubes (SWNTs) in the liquid phase is their hydrophobicity-induced aggregation, which prevents utilization of the unique physical and chemical properties of single SWNTs. Recently it has been found that lysophospholipids, or single-tailed phospholipids, can readily form supramolecular complexes with SWNTs and the resultant SWNT solubility is superior to that provided by nucleic acids, proteins, and surfactants such as sodium dodecyl sulfate. Using transmission electron microscopy, lysophospholipids were observed forming striations on SWNTs in a vacuum. Although the morphology of the striations seemingly favors the hemimicellular model, serious doubts remain about the arrangement of individual lipids within the striations. Here we present an in silico study of the binding of zwitterionic lysophosphatidylcholine to an SWNT. We present compelling evidence that the binding of lipid surfactants to cylindrical nanostructures in the liquid phase does not obey any of the three popular models in the literature. Understanding the binding of lipid amphiphiles to SWNTs facilitates the bottom-up design of novel nanostructures for supramolecular chemistry and nanotechnology and fuels new field studies of nanotoxicity and nanomedicine.

  16. 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...... where accurate pH and carbonate alkalinity determinations are difficult to obtain, such as saline waters and waters of high organic loadings....

  17. Reply to ``Comment on `Imaging the atomic orbitals of carbon atomic chains with field-emission electron microscopy' ''

    Science.gov (United States)

    Mikhailovskij, I. M.; Sadanov, E. V.; Mazilova, T. I.; Ksenofontov, V. A.; Velicodnaja, O. A.

    2010-03-01

    In our recent paper [I. M. Mikhailovskij, E. V. Sadanov, T. I. Mazilova, V. A. Ksenofontov, and O. A. Velicodnaja, Phys. Rev. B 80, 165404 (2009)], we have presented evidence for field emission from individual orbitals of self-standing carbon chains, which can be used for real-space imaging of the end-atom orbitals with a field-emission electron microscope (FEEM). In this reply to the preceding Comment, we refer to the issues brought up there, which concern the viewpoint that the observed spontaneous mutual transformations of FEEM patterns have been attributed to the ligand-induced symmetry breaking by calling attention to the role of hydrogen atoms unavoidable in most nanostructured carbon materials.

  18. Quantitative Atomic Force Microscopy with Carbon Monoxide Terminated Tips

    OpenAIRE

    Sun, Zhixiang; Boneschanscher, Mark P.; Swart, Ingmar; Vanmaekelbergh, Daniel; Liljeroth, Peter

    2011-01-01

    Noncontact atomic force microscopy (AFM) has recently progressed tremendously in achieving atomic resolution imaging through the use of small oscillation amplitudes and well-defined modification of the tip apex. In particular, it has been shown that picking up simple inorganic molecules (such as CO) by the AFM tip leads to a well-defined tip apex and to enhanced image resolution. Here, we use the same approach to study the three-dimensional intermolecular interaction potential between two mol...

  19. 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

  20. Intravenous injection of unfunctionalized carbon-based nanomaterials confirms the minimal toxicity observed in aqueous and dietary exposures in juvenile rainbow trout (Oncorhynchus mykiss).

    Science.gov (United States)

    Boyle, David; Sutton, Paul A; Handy, Richard D; Henry, Theodore B

    2018-01-01

    Numerous ecotoxicology studies of carbon-based nanomaterials (CNMs) have been conducted in fishes; however, different approaches have been used to make CNM dispersions and dose tanks for aqueous exposures, and to prepare food containing CNMs for dietary studies. This diversity of experimental methods has led to conflicting results and difficulties in comparing studies. The objective of the present study was to evaluate intravenous injection of unfunctionalized CNMs in rainbow trout (Oncorhynchus mykiss), as a means of delivering a known internal dose, on tissue biochemistry and histopathological lesions; then, subsequently, to compare the results with our previous work on aqueous and dietary exposures of rainbow trout to CNMs. Rainbow trout were injected in the caudal vein with corn oil dispersions of 200 μg (approximately 1 μg g-1) of either the fullerene C60, single-walled carbon nanotubes (SWCNTs), or amorphous carbon black. After 96 h, injected fish were euthanized and tissue samples collected for biochemistry and histology. Histological examination of the kidney of fish injected intravenously indicated the presence of black material consistent with the injected carbon treatments. However, there were no additional lesions associated with CNM exposure compared to controls. There were also no significant changes in haematology, or ionoregulatory disturbance in blood plasma among the intravenously injected fish. Significant elevation in lipid peroxidation (thiobarbituric acid reactive substances TBARS) was detected only in kidney and spleen of fish injected with SWCNTs, but not the other carbon treatments. The elevated TBARS following injection contrasted with CNMs delivered via aqueous or dietary routes in our previous studies, suggesting that the latter exposure routes may not lead to absorption and toxicity in the internal tissues. Comparison of the effects of injected CNMs with aqueous and dietary CNMs exposures indicates that these materials are of

  1. Adsorption Efficiency of Iron Modified Carbons for Removal of Pb(II Ions from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Mohammad Hossein Salmani

    2016-06-01

    Full Text Available Abstract Introduction: The Lead causes severe damage to several systems of the body, especially to bony tissues. Until now, several low-cost biosorbents have been studied for removal of heavy metal ions from aqueous solutions. In the present study, carbonized pomegranate peels modified with Fe2+ and Fe3+ ions and then it was investigated for removal of Pb(II ions from aqueous solution. Materials and methods: the washed granola of pomegranate peel was separately socked with FeCl3 and FeCl2 solutions for 24 h. Then, the granules were carbonized at 400 ºC for 3 h in a programmable furnace in the atmosphere of nitrogen. The adsorption experiments were carried out for two types of iron-modified carbons by batch adsorption using one variable at a time procedures. Results: The optimum conditions were found as contact time 90 min, initial concentration 50 mg/l, and adsorbent dose, 1.00 g/100 ml solution. Maximum removal efficiency was calculated as 84% and 89% for Fe3+ and Fe2+ impregnated pomegranate peel carbons respectively. Conclusion: The iron treatment pomegranate peel carbons modified their surfaces for adsorption of heavy metals. The results showed that chemical modification of the low-cost adsorbents originating from agricultural waste has stood out for metal removal capabilities.

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

    Directory of Open Access Journals (Sweden)

    Tamara Minović Arsić

    2016-03-01

    Full Text Available 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 arsenic(III on carbon cryogel. Adsorption dose experiments showed that the mass of the adsorbent was reduced for 20 times, in comparison with pure CC, for the same amount of adsorbed arsenic(III ions. BET isotherm was used to interpret the experimental data for modelling liquid phase adsorption.

  3. Establishing the fair allocation of international aviation carbon emission rights

    Directory of Open Access Journals (Sweden)

    Feng-Cai Zhao

    2014-09-01

    Full Text Available To identify potentially unfair use of international aviation carbon emission rights in different countries, this paper presents a carbon Lorenz curve and Gini coefficient, constructed on the basis of historical cumulative international aviation CO2 emissions per capita. The study follows a methodology adapted from the research into fair income allocation. The results of these calculations show that there has been vast unfairness surrounding international aviation carbon emissions in the past, and that this unfairness has been partially hidden by a delay in accumulative start dates. A solution to this problem, allowing fair allocation of carbon emissions, is the key to building a mechanism for the reduction of global international aviation emissions. This study proposes a fair method for allocating emission rights, based on a responsibility-capacity index. Taking a goal of carbon-neutral growth by 2020 as an example, the degree of carbon emission reduction expected from different countries by 2021 is calculated using the proposed method.

  4. Formation and composition of adsorbates on hydrophobic carbon surfaces from aqueous laccase-maltodextrin mixture suspension

    Energy Technology Data Exchange (ETDEWEB)

    Corrales Ureña, Yendry Regina, E-mail: yendry386@hotmail.com [UNESP São Paulo State University, Av. Eng. Luiz Edmundo Carrijo Coube, 14-01, Bauru, São Paulo (Brazil); Fraunhofer Institute for Manufacturing Technology and Advanced Materials IFAM, Wiener Strasse 12, 28359 Bremen (Germany); Lisboa-Filho, Paulo Noronha [UNESP São Paulo State University, Av. Eng. Luiz Edmundo Carrijo Coube, 14-01, Bauru, São Paulo (Brazil); Szardenings, Michael [Fraunhofer Institute for Cell Therapy and Immunology IZI, Perlickstrasse 1, 04103 Leipzig (Germany); Gätjen, Linda; Noeske, Paul-Ludwig Michael; Rischka, Klaus [Fraunhofer Institute for Manufacturing Technology and Advanced Materials IFAM, Wiener Strasse 12, 28359 Bremen (Germany)

    2016-11-01

    Highlights: • Less than 10 nm layer formed on carbon based materials composed by laccase and maltodextrin. • Improvement of the wettability of carbon based materials. • A protein-polysaccharide biofilm layer formation at solid liquid interface. • Stable layers formed under buffer and water rinsing. - Abstract: A robust procedure for the surface bio-functionalization of carbon surfaces was developed. It consists on the modification of carbon materials in contact with an aqueous suspension of the enzyme laccase from Trametes versicolor and the lyophilization agent maltodextrin, with the pH value adjusted close to the isoelectric point of the enzyme. We report in-situ investigations applying Quartz Crystal Microbalance with Dissipation (QCM-D) for carbon-coated sensor surfaces and, moreover, ex-situ measurements with static contact angle measurements, X-ray Photoelectron Spectroscopy (XPS) and Scanning Force Microscopy (SFM) for smooth Highly Oriented Pyrolytic Graphite (HOPG) substrates, for contact times between the enzyme formulation and the carbon material surface ranging from 20 s to 24 h. QCM-D studies reveals the formation of rigid layer of biomaterial, a few nanometers thin, which shows a strongly improved wettability of the substrate surface upon contact angle measurements. Following spectroscopic characterization, these layers are composed of mixtures of laccase and maltodextrin. The formation of these adsorbates is attributed to attractive interactions between laccase, the maltodextrin-based lyophilization agent and the hydrophobic carbon surfaces; a short-term contact between the aqueous laccase mixture suspension and HOPG surfaces is shown to merely result in de-wetting patterns influencing the results of contact angle measurements. The new enzyme-based surface modification of carbon-based materials is suggested to be applicable for the improvement of not only the wettability of low energy substrate surfaces with fluid formulations like coatings

  5. The Use of Contact Mode Atomic Force Microscopy in Aqueous Medium for Structural Analysis of Spinach Photosynthetic Complexes.

    Science.gov (United States)

    Phuthong, Witchukorn; Huang, Zubin; Wittkopp, Tyler M; Sznee, Kinga; Heinnickel, Mark L; Dekker, Jan P; Frese, Raoul N; Prinz, Fritz B; Grossman, Arthur R

    2015-10-01

    To investigate the dynamics of photosynthetic pigment-protein complexes in vascular plants at high resolution in an aqueous environment, membrane-protruding oxygen-evolving complexes (OECs) associated with photosystem II (PSII) on spinach (Spinacia oleracea) grana membranes were examined using contact mode atomic force microscopy. This study represents, to our knowledge, the first use of atomic force microscopy to distinguish the putative large extrinsic loop of Photosystem II CP47 reaction center protein (CP47) from the putative oxygen-evolving enhancer proteins 1, 2, and 3 (PsbO, PsbP, and PsbQ) and large extrinsic loop of Photosystem II CP43 reaction center protein (CP43) in the PSII-OEC extrinsic domains of grana membranes under conditions resulting in the disordered arrangement of PSII-OEC particles. Moreover, we observed uncharacterized membrane particles that, based on their physical characteristics and electrophoretic analysis of the polypeptides associated with the grana samples, are hypothesized to be a domain of photosystem I that protrudes from the stromal face of single thylakoid bilayers. Our results are interpreted in the context of the results of others that were obtained using cryo-electron microscopy (and single particle analysis), negative staining and freeze-fracture electron microscopy, as well as previous atomic force microscopy studies. © 2015 American Society of Plant Biologists. All Rights Reserved.

  6. The Use of Contact Mode Atomic Force Microscopy in Aqueous Medium for Structural Analysis of Spinach Photosynthetic Complexes1[OPEN

    Science.gov (United States)

    Phuthong, Witchukorn; Huang, Zubin; Wittkopp, Tyler M.; Sznee, Kinga; Heinnickel, Mark L.; Dekker, Jan P.; Frese, Raoul N.; Prinz, Fritz B.; Grossman, Arthur R.

    2015-01-01

    To investigate the dynamics of photosynthetic pigment-protein complexes in vascular plants at high resolution in an aqueous environment, membrane-protruding oxygen-evolving complexes (OECs) associated with photosystem II (PSII) on spinach (Spinacia oleracea) grana membranes were examined using contact mode atomic force microscopy. This study represents, to our knowledge, the first use of atomic force microscopy to distinguish the putative large extrinsic loop of Photosystem II CP47 reaction center protein (CP47) from the putative oxygen-evolving enhancer proteins 1, 2, and 3 (PsbO, PsbP, and PsbQ) and large extrinsic loop of Photosystem II CP43 reaction center protein (CP43) in the PSII-OEC extrinsic domains of grana membranes under conditions resulting in the disordered arrangement of PSII-OEC particles. Moreover, we observed uncharacterized membrane particles that, based on their physical characteristics and electrophoretic analysis of the polypeptides associated with the grana samples, are hypothesized to be a domain of photosystem I that protrudes from the stromal face of single thylakoid bilayers. Our results are interpreted in the context of the results of others that were obtained using cryo-electron microscopy (and single particle analysis), negative staining and freeze-fracture electron microscopy, as well as previous atomic force microscopy studies. PMID:26220954

  7. Materials Properties at Internal Interfaces: Fundamental Atomic Issues

    Energy Technology Data Exchange (ETDEWEB)

    Browning, Nigel D. [Univ. of California, Davis, CA (United States)

    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.

  8. Atomic Layer Deposition on Carbon Nanotubes and their Assemblies

    Science.gov (United States)

    Stano, Kelly Lynn

    Global issues related to energy and the environment have motivated development of advanced material solutions outside of traditional metals ceramics, and polymers. Taking inspiration from composites, where the combination of two or more materials often yields superior properties, the field of organic-inorganic hybrids has recently emerged. Carbon nanotube (CNT)-inorganic hybrids have drawn widespread and increasing interest in recent years due to their multifunctionality and potential impact across several technologically important application areas. Before the impacts of CNT-inorganic hybrids can be realized however, processing techniques must be developed for their scalable production. Optimization in chemical vapor deposition (CVD) methods for synthesis of CNTs and vertically aligned CNT arrays has created production routes both high throughput and economically feasible. Additionally, control of CVD parameters has allowed for growth of CNT arrays that are able to be drawn into aligned sheets and further processed to form a variety of aligned 1, 2, and 3-dimensional bulk assemblies including ribbons, yarns, and foams. To date, there have only been a few studies on utilizing these bulk assemblies for the production of CNT-inorganic hybrids. Wet chemical methods traditionally used for fabricating CNT-inorganic hybrids are largely incompatible with CNT assemblies, since wetting and drying the delicate structures with solvents can destroy their structure. It is therefore necessary to investigate alternative processing strategies in order to advance the field of CNT-inorganic hybrids. In this dissertation, atomic layer deposition (ALD) is evaluated as a synthetic route for the production of large-scale CNT-metal oxide hybrids as well as pure metal oxide architectures utilizing CNT arrays, ribbons, and ultralow density foams as deposition templates. Nucleation and growth behavior of alumina was evaluated as a function of CNT surface chemistry. While highly graphitic

  9. 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.

  10. Direct determination of carbon dioxide in aqueous solution using mid-infrared quantum cascade lasers.

    Science.gov (United States)

    Schaden, S; Haberkorn, M; Frank, J; Baena, J R; Lendl, B

    2004-06-01

    A method for the direct determination of carbon dioxide in aqueous solutions using a room-temperature mid-infrared (MIR) quantum cascade laser at 2330 cm(-1) is reported. The absorption values of different carbon dioxide concentrations were measured in a 119 microm CaF2 flow-through cell. An optical system made of parabolic mirrors was used to probe the flow cell and to focus the laser beam on the mercury cadmium telluride (MCT) detector. Aqueous carbon dioxide standards were prepared by feeding different mixtures of gaseous N2 and CO2 through wash bottles at controlled temperature. The concentration of the dissolved CO2 was calculated according to Henry's law, taking into account the temperature and the partial pressure of CO2. The carbon dioxide standards were connected via a selection valve to a peristaltic pump for subsequent, automated measurement in the flow-through cell. A calibration curve was obtained in the range of 0.338 to 1.350 g/L CO2 with a standard deviation of the method sxo equal to 19.4 mg/L CO2. The limit of detection was calculated as three times the baseline noise over time and was determined to be 39 mg/L.

  11. Superior capacitive performance of hydrochar-based porous carbons in aqueous electrolytes.

    Science.gov (United States)

    Fuertes, Antonio B; Sevilla, Marta

    2015-03-01

    Biomass-based highly porous carbons with excellent performances in aqueous electrolyte-based supercapacitors have been developed. The synthesis of these materials is based on the chemical activation of biomass-based hydrochar. The addition of melamine to the activation mixture leads to porous carbons with a porosity consisting of micropores/small mesopores. Furthermore, melamine promotes the introduction of nitrogen heteroatoms in the carbon framework, along with abundant oxygen functionalities, to improve the wettability. The materials produced in the presence or absence of melamine exhibit high specific capacitances in aqueous electrolytes (>270 F g(-1) in H2 SO4 and >190 F g(-1) in Li2SO4). Additionally, the mesopores present in the melamine-based micro-/mesoporous carbons notably improve the ion-transport kinetics, especially in Li2SO4. Furthermore, in Li2SO4, they remain stable up to a cell voltage of 1.6 V; thus exhibiting superior energy and power characteristics than those in H2 SO4. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Migration Mechanism for Atomic Hydrogen in Porous Carbon Materials

    Energy Technology Data Exchange (ETDEWEB)

    Narayanan, B.; Zhao, Y. F.; Ciobanu, C. V.

    2012-05-14

    To explain the fast kinetics of H in porous carbon, we propose that the migration relies on H hopping from a carbon nanotube (CNT) to another. Using density functional theory, we have found that the barrier for H hopping becomes smaller than that for diffusion along a tube for certain CNT separations, decreasting to less than 0.5 eV for separations of -3.1 {angstrom}. Such significant reduction occurs irrespective of radius, chirality, registry, and orientation of the two CNTs: the diffusion is thus facilitated by the porous nature of the material itself. The mechanism proposed is applicable for any porous carbon-based nanomaterials.

  13. ADSORPTION OF FOOD COLORING ALLURA RED DYE (E129 FROM AQUEOUS SOLUTIONS USING ACTIVATED CARBON

    Directory of Open Access Journals (Sweden)

    Saad A Alkahtani

    2017-09-01

    Full Text Available The adsorption behavior of Allura red (E129 from aqueous solutions onto activated carbon was successfully investigated. All factors affecting the adsorption process were carefully studied and the conditions were optimized. Adsorption of E129 onto activated carbon was found to increase by decreasing the mass of activated carbon, pH and ionic strength of the solution and by increasing temperature. The adsorption capacity of the activated carbon for Allura red was relatively high. Under the optimum conditions, the maximum adsorption capacity for E129 dye was 72.85 mg/g. Three adsorption models; Langmuir, Freundlich and Temkin model were investigated regarding the adsorption of E129. The models’ parameters KL, qm, R2, (n were determined and found to be 0.0222, 72.85 mg/g, 0.9057-0.9984, and 0.992, respectively. Also, pseudo first and second-order kinetic models were tested to determine the best-fit model to the adsorption of E129 dye onto activated carbon. The results showed that the adsorption of E129 onto activated carbon obeyed both the Freundlich isotherm and pseudo second-order kinetic models. Moreover, thermodynamic studies indicated that the adsorption of E129 dye onto the activated carbon was spontaneous. 

  14. Metal-free supercapacitor with aqueous electrolyte and low-cost carbon materials

    Science.gov (United States)

    Blomquist, Nicklas; Wells, Thomas; Andres, Britta; Bäckström, Joakim; Forsberg, Sven; Olin, Håkan

    2017-01-01

    Electric double-layer capacitors (EDLCs) or supercapacitors (SCs) are fast energy storage devices with high pulse efficiency and superior cyclability, which makes them useful in various applications including electronics, vehicles and grids. Aqueous SCs are considered to be more environmentally friendly than those based on organic electrolytes. Because of the corrosive nature of the aqueous environment, however, expensive electrochemically stable materials are needed for the current collectors and electrodes in aqueous SCs. This results in high costs for a given energy-storage capacity. To address this, we developed a novel low-cost aqueous SC using graphite foil as the current collector and a mix of graphene, nanographite, simple water-purification carbons and nanocellulose as electrodes. The electrodes were coated directly onto the graphite foil by using casting frames and the SCs were assembled in a pouch cell design. With this approach, we achieved a material cost reduction of greater than 90% while maintaining approximately one-half of the specific capacitance of a commercial unit, thus demonstrating that the proposed SC can be an environmentally friendly, low-cost alternative to conventional SCs.

  15. Effect of Axial Torsion on sp Carbon Atomic Wires

    OpenAIRE

    Ravagnan, L.; Manini, N.; Cinquanta, E.; Onida, G.; Motta, C.; Sangalli, D.; Bordoni, A; Devetta, M.; Piseri, P.; Milani, P.

    2009-01-01

    Ab-initio calculations within Density Functional Theory combined with experimental Raman spectra on cluster-beam deposited pure carbon films provide a consistent picture of sp-carbon chains stabilized by sp^3 or sp^2 terminations, the latter being sensitive to torsional strain. This unexplored effect promises many exciting applications since it allows one to modify the conductive states near the Fermi level and to switch on and off the on-chain pi-electron magnetism.

  16. Effect of axial torsion on sp carbon atomic wires.

    Science.gov (United States)

    Ravagnan, Luca; Manini, Nicola; Cinquanta, Eugenio; Onida, Giovanni; Sangalli, Davide; Motta, Carlo; Devetta, Michele; Bordoni, Andrea; Piseri, Paolo; Milani, Paolo

    2009-06-19

    Ab initio calculations within density-functional theory combined with experimental Raman spectra on cluster-beam deposited pure-carbon films provide a consistent picture of sp-carbon chains stabilized by sp;{3} or sp;{2} terminations, the latter being sensitive to torsional strain. This unexplored effect promises many exciting applications since it allows one to modify the conductive states near the Fermi level and to switch on and off the on-chain pi-electron magnetism.

  17. Growth and Destruction of PAH Molecules in Reactions with Carbon Atoms

    Energy Technology Data Exchange (ETDEWEB)

    Krasnokutski, Serge A.; Huisken, Friedrich; Jäger, Cornelia; Henning, Thomas [Laboratory Astrophysics Group of the Max Planck Institute for Astronomy at the Friedrich Schiller University Jena, Helmholtzweg 3, D-07743 Jena (Germany)

    2017-02-10

    A very high abundance of atomic carbon in the interstellar medium (ISM), and the high reactivity of these species toward different hydrocarbon molecules including benzene, raise questions regarding the stability of polycyclic aromatic hydrocarbon (PAH) molecules in space. To test the efficiency of destruction of PAH molecules via reactions with atomic carbon, we performed a set of laboratory and computational studies of the reactions of naphthalene, anthracene, and coronene molecules with carbon atoms in the ground state. The reactions were investigated in liquid helium droplets at T = 0.37 K and by quantum chemical computations. Our studies suggest that all small and all large catacondensed PAHs react barrierlessly with atomic carbon, and therefore should be efficiently destroyed by such reactions in a broad temperature range. At the same time, large compact pericondensed PAHs should be more inert toward such a reaction. In addition, taking into account their higher photostability, much higher abundances of pericondensed PAHs should be expected in various astrophysical environments. The barrierless reactions between carbon atoms and small PAHs also suggest that, in the ISM, these reactions could lead to the bottom-up formation of PAH molecules.

  18. Characterization of local hydrophobicity on sapphire (0001) surfaces in aqueous environment by colloidal probe atomic force microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Wada, Tomoya; Yamazaki, Kenji; Isono, Toshinari; Ogino, Toshio, E-mail: ogino-toshio-rx@ynu.ac.jp

    2017-02-28

    Highlights: • Local hydrophobicity of phase-separated sapphire (0001) surfaces was investigated. • These surfaces are featured by coexistence of hydrophilic and hydrophobic domains. • Each domain was characterized by colloidal probe atomic force microscopy in water. • Both domains can be distinguished by adhesive forces of the probe to the surfaces. • Characterization in aqueous environment is important in bio-applications of sapphire. - Abstract: Sapphire (0001) surfaces exhibit a phase-separation into hydrophobic and hydrophilic domains upon high-temperature annealing, which were previously distinguished by the thickness of adsorbed water layers in air using atomic force microscopy (AFM). To characterize their local surface hydrophobicity in aqueous environment, we used AFM equipped with a colloidal probe and measured the local adhesive force between each sapphire domain and a hydrophilic SiO{sub 2} probe surface, or a hydrophobic polystyrene one. Two data acquisition modes for statistical analyses were used: one is force measurements at different positions of the surface and the other repeated measurement at a fixed position. We found that adhesive force measurements using the polystyrene probe allow us to distinctly separate the hydrophilic and hydrophobic domains. The dispersion in the force measurement data at different positions of the surface is larger than that in the repeated measurements at a fixed position. It indicates that the adhesive force measurement is repeatable although their data dispersion for the measurement positions is relatively large. From these results, we can conclude that the hydrophilic and hydrophobic domains on the sapphire (0001) surfaces are distinguished by a difference in their hydration degrees.

  19. Effect of textural and chemical characteristics of activated carbons on phenol adsorption in aqueous solutions

    Directory of Open Access Journals (Sweden)

    Vargas Diana P.

    2017-12-01

    Full Text Available The effect of textural and chemical properties such as: surface area, pore volume and chemical groups content of the granular activated carbon and monoliths on phenol adsorption in aqueous solutions was studied. Granular activated carbon and monolith samples were produced by chemical activation. They were characterized by using N2 adsorption at 77 K, CO2 adsorption at 273 K, Boehm Titrations and immersion calorimetry in phenol solutions. Microporous materials with different pore size distribution, surface area between 516 and 1685 m2 g−1 and pore volumes between 0.24 and 0.58 cm3 g−1 were obtained. Phenol adsorption capacity of the activated carbon materials increased with increasing BET surface area and pore volume, and is favored by their surface functional groups that act as electron donors. Phenol adsorption capacities are in ranged between 73.5 and 389.4 mg · g−1.

  20. Imaging the response of individual carbon nanotubes to polarized light in aqueous environments

    Science.gov (United States)

    Walker, Bryant; Brintlinger, Todd; Fuhrer, Michael S.; Cumings, John; Hobbie, Erik

    2007-03-01

    Individual carbon nanotubes are grown using chemical vapor deposition (methane-ethylene carrier gas and iron nitrate catalyst), freely suspended in an aqueous solution using a surfactant (sodium dodecyl sulfate), and imaged in an optical microscope using either fluorescent dye (PKH67 and PKH23) or intrinsic near-infrared fluorescence. Freely suspended, individual carbon nanotubes of length 1-8 micrometers show an increasing response to illuminating light as the polarization becomes parallel to tube axis. More intriguingly, some of the carbon nanotubes are found to collapse and fold under 10-30 seconds of illumination, with increasing tube length showing longer time-to-collapse. Unperturbed persistence lengths in these nanotubes are estimated to be 200-300 micrometers.

  1. Partial atomic multipoles for internally consistent microelectrostatic calculations.

    Science.gov (United States)

    Snamina, Mateusz; Mazur, Grzegorz; Petelenz, Piotr

    2017-10-30

    An extension of the extant microelectrostatic methodologies, based on the concept of distributed generalized polarizability matrix derived from the Coupled Perturbed Hartree-Fock (CPHF) equations, is proposed for self-consistent calculation of charge carrier and charge-transfer (CT) state electrostatic energies in molecular solids, including the doped, defected and disordered ones. The CPHF equations are solved only once and the generalized molecular polarizability they yield enables low cost iterations that mutually adjust the molecular electronic distributions and the local electric field in which the molecules are immersed. The approach offers a precise picture of molecular charge densities, accounting for atomic partial multipoles up to order 2, which allows one to reproduce the recently reported large charge-quadrupole contributions to CT state energies in low-symmetry local environments. It is particularly well suited for repetitive calculations for large clusters (up to 300,000 atoms), and may potentially be useful for describing electrostatic solvent effects. © 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.

  2. Strain-induced metal-semiconductor transition observed in atomic carbon chains.

    Science.gov (United States)

    La Torre, A; Botello-Mendez, A; Baaziz, W; Charlier, J-C; Banhart, F

    2015-03-30

    Carbyne, the sp(1)-hybridized phase of carbon, is still a missing link in the family of carbon allotropes. While the bulk phases of carbyne remain elusive, the elementary constituents, that is, linear chains of carbon atoms, have already been observed using the electron microscope. Isolated atomic chains are highly interesting one-dimensional conductors that have stimulated considerable theoretical work. Experimental information, however, is still very limited. Here we show electrical measurements and first-principles transport calculations on monoatomic carbon chains. When the 1D system is under strain, the chains are semiconducting corresponding to the polyyne structure with alternating bond lengths. Conversely, when the chain is unstrained, the ohmic behaviour of metallic cumulene with uniform bond lengths is observed. This confirms the recent prediction of a metal-insulator transition that is induced by strain. The key role of the contacting leads explains the rectifying behaviour measured in monoatomic carbon chains in a nonsymmetric contact configuration.

  3. Strain-induced metal–semiconductor transition observed in atomic carbon chains

    Science.gov (United States)

    La Torre, A.; Botello-Mendez, A.; Baaziz, W.; Charlier, J. -C.; Banhart, F.

    2015-01-01

    Carbyne, the sp1-hybridized phase of carbon, is still a missing link in the family of carbon allotropes. While the bulk phases of carbyne remain elusive, the elementary constituents, that is, linear chains of carbon atoms, have already been observed using the electron microscope. Isolated atomic chains are highly interesting one-dimensional conductors that have stimulated considerable theoretical work. Experimental information, however, is still very limited. Here we show electrical measurements and first-principles transport calculations on monoatomic carbon chains. When the 1D system is under strain, the chains are semiconducting corresponding to the polyyne structure with alternating bond lengths. Conversely, when the chain is unstrained, the ohmic behaviour of metallic cumulene with uniform bond lengths is observed. This confirms the recent prediction of a metal–insulator transition that is induced by strain. The key role of the contacting leads explains the rectifying behaviour measured in monoatomic carbon chains in a nonsymmetric contact configuration. PMID:25818506

  4. Removal of trihalomethanes from aqueous solution through armchair carbon nanotubes: a molecular dynamics study.

    Science.gov (United States)

    Azamat, Jafar; Khataee, Alireza; Joo, Sang Woo; Yin, Binfeng

    2015-04-01

    Molecular dynamics simulations were performed to investigate the removal of trihalomethanes (THMs) including CH3Cl, CH2Cl2 and CHCl3 from aqueous solutions by armchair carbon nanotubes (CNTs) under induced pressure. The studied system involved the armchair CNTs embedded between two graphene sheets with an aqueous solution of THMs in the simulation box. An external pressure was applied to the system along the z-axis of the simulation box. Six types of armchair CNTs with different diameter were used in this work, included (4,4), (5,5), (6,6), (7,7), (8,8) and (9,9) CNTs. The results of molecular dynamics simulation display that the armchair CNTs behave differently relative to THMs and water molecules. The permeation of THMs and water molecules through the armchair CNTs was dependent on the diameter of CNTs and the applied pressure. Copyright © 2015 Elsevier Inc. All rights reserved.

  5. Chirality Separation of Single-Wall Carbon Nanotubes using Aqueous Two-Phase Extraction

    Science.gov (United States)

    Fagan, Jeffrey

    2014-03-01

    Aqueous two-phase extraction (ATPE) was recently demonstrated to enable the separation of individual species of single-wall carbon nanotubes (SWCNTs) across the separated phases. In this presentation I will describe the use of a dextran - polyethylene glycol aqueous two-phase system along with a separation scheme of varying surfactant concentrations to enable isolation at high purity of specific small diameter SWCNT species. Separation by ATPE is rapid and robust, with a remarkable tunability that allows isolation of most single nanotube chiralities at high purity. Choice of surfactant(s), temperature, polymer concentrations, and the addition of small molecule salts can all be used to tune the exact partitioning of single SWCNT species between the two phases.

  6. Hydrogen-atom abstraction reactions by manganese(V)- and manganese(IV)-oxo porphyrin complexes in aqueous solution.

    Science.gov (United States)

    Arunkumar, Chellaiah; Lee, Yong-Min; Lee, Jung Yoon; Fukuzumi, Shunichi; Nam, Wonwoo

    2009-11-02

    High-valent manganese(IV or V)-oxo porphyrins are considered as reactive intermediates in the oxidation of organic substrates by manganese porphyrin catalysts. We have generated Mn(V)- and Mn(IV)-oxo porphyrins in basic aqueous solution and investigated their reactivities in C-H bond activation of hydrocarbons. We now report that Mn(V)- and Mn(IV)-oxo porphyrins are capable of activating C-H bonds of alkylaromatics, with the reactivity order of Mn(V)-oxo>Mn(IV)-oxo; the reactivity of a Mn(V)-oxo complex is 150 times greater than that of a Mn(IV)-oxo complex in the oxidation of xanthene. The C-H bond activation of alkylaromatics by the Mn(V)- and Mn(IV)-oxo porphyrins is proposed to occur through a hydrogen-atom abstraction, based on the observations of a good linear correlation between the reaction rates and the C-H bond dissociation energy (BDE) of substrates and high kinetic isotope effect (KIE) values in the oxidation of xanthene and dihydroanthracene (DHA). We have demonstrated that the disproportionation of Mn(IV)-oxo porphyrins to Mn(V)-oxo and Mn(III) porphyrins is not a feasible pathway in basic aqueous solution and that Mn(IV)-oxo porphyrins are able to abstract hydrogen atoms from alkylaromatics. The C-H bond activation of alkylaromatics by Mn(V)- and Mn(IV)-oxo species proceeds through a one-electron process, in which a Mn(IV)-oxo porphyrin is formed as a product in the C-H bond activation by a Mn(V)-oxo porphyrin, followed by a further reaction of the Mn(IV)-oxo porphyrin with substrates that results in the formation of a Mn(III) porphyrin complex. This result is in contrast to the oxidation of sulfides by the Mn(V)-oxo porphyrin, in which the oxidation of thioanisole by the Mn(V)-oxo complex produces the starting Mn(III) porphyrin and thioanisole oxide. This result indicates that the oxidation of sulfides by the Mn(V)-oxo species occurs by means of a two-electron oxidation process. In contrast, a Mn(IV)-oxo porphyrin complex is not capable of oxidizing

  7. Competitive adsorption of phenolic compounds from aqueous solution using sludge-based activated carbon.

    Science.gov (United States)

    Mohamed, E F; Andriantsiferana, C; Wilhelm, A M; Delmas, H

    2011-01-01

    Preparation of activated carbon from sewage sludge is a promising approach to produce cheap and efficient adsorbent for pollutants removal as well as to dispose of sewage sludge. The first objective of this study was to investigate the physical and chemical properties (BET surface area, ash and elemental content, surface functional groups by Boehm titration and weight loss by thermogravimetric analysis) of the sludge-based activated carbon (SBAC) so as to give a basic understanding of its structure and to compare to those of two commercial activated carbons, PICA S23 and F22. The second and main objective was to evaluate the performance of SBAC for single and competitive adsorption of four substituted phenols (p-nitrophenol, p-chlorophenol, p-hydroxy benzoic acid and phenol) from their aqueous solutions. The results indicated that, despite moderate micropore and mesopore surface areas, SBAC had remarkable adsorption capacity for phenols, though less than PICA carbons. Uptake of the phenolic compound was found to be dependent on both the porosity and surface chemistry of the carbons. Furthermore, the electronegativity and the hydrophobicity of the adsorbate have significant influence on the adsorption capacity. The Langmuir and Freundlich models were used for the mathematical description of the adsorption equilibrium for single-solute isotherms. Moreover, the Langmuir-Freundlich model gave satisfactory results for describing multicomponent system isotherms. The capacity of the studied activated carbons to adsorb phenols from a multi-solute system was in the following order: p-nitrophenol > p-chlorophenol > PHBA > phenol.

  8. Room-temperature aqueous plasma electrolyzing Al2O3 nano-coating on carbon fiber

    Science.gov (United States)

    Zhang, Yuping; Meng, Yang; Shen, Yonghua; Chen, Weiwei; Cheng, Huanwu; Wang, Lu

    2017-10-01

    A novel room-temperature aqueous plasma electrolysis technique has been developed in order to prepared Al2O3 nano-coating on each fiber within a carbon fiber bundle. The microstructure and formation mechanism of the Al2O3 nano-coating were systematically investigated. The oxidation resistance and tensile strength of the Al2O3-coated carbon fiber was measured at elevated temperatures. It showed that the dense Al2O3 nano-coating was relatively uniformly deposited with 80-120 nm in thickness. The Al2O3 nano-coating effectively protected the carbon fiber, evidenced by the slower oxidation rate and significant increase of the burn-out temperature from 800 °C to 950 °C. Although the bare carbon fiber remained ∼25 wt.% after oxidation at 700 °C for 20 min, a full destruction was observed, evidenced by the ∼0 GPa of the tensile strength, compared to ∼1.3 GPa of the Al2O3-coated carbon fiber due to the effective protection from the Al2O3 nano-coating. The formation mechanism of the Al2O3 nano-coating on carbon fiber was schematically established mainly based on the physic-chemical effect in the cathodic plasma arc zone.

  9. Integrating Carbon Nanotubes For Atomic Force Microscopy Imaging Applications

    Science.gov (United States)

    Ye, Qi; Cassell, Alan M.; Liu, Hongbing; Han, Jie; Meyyappan, Meyya

    2004-01-01

    Carbon nanotube (CNT) related nanostructures possess remarkable electrical, mechanical, and thermal properties. To produce these nanostructures for real world applications, a large-scale controlled growth of carbon nanotubes is crucial for the integration and fabrication of nanodevices and nanosensors. We have taken the approach of integrating nanopatterning and nanomaterials synthesis with traditional silicon micro fabrication techniques. This integration requires a catalyst or nanomaterial protection scheme. In this paper, we report our recent work on fabricating wafer-scale carbon nanotube AFM cantilever probe tips. We will address the design and fabrication considerations in detail, and present the preliminary scanning probe test results. This work may serve as an example of rational design, fabrication, and integration of nanomaterials for advanced nanodevice and nanosensor applications.

  10. 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.

  11. Amoxicillin removal from aqueous solution using activated carbon prepared by chemical activation of olive stone.

    Science.gov (United States)

    Limousy, Lionel; Ghouma, Imen; Ouederni, Abdelmottaleb; Jeguirim, Mejdi

    2017-04-01

    A chemical-activated carbon (CAC) was prepared by phosphoric acid activation of olive stone. The CAC was characterized using various analytical techniques and evaluated for the removal of amoxicillin from aqueous solutions under different operating conditions (initial concentration, 12.5-100 mg L -1 , temperature, 20-25 °C, contact time, 0-7000 min). The CAC characterization indicates that it is a microporous carbon with a specific surface area of 1174 m 2 /g and a pore volume of 0.46 cm 3 /g and contains essentially acidic functional groups. The adsorption tests indicated that 93 % of amoxicillin was removed at 20 °C for 25 mg L -1 initial concentration. Moreover, it was found that adsorption capacity increased with contact time and temperature. Kinetic study shows that the highest correlation was obtained for the pseudo-second-order kinetic model, which confirms that the process of adsorption of amoxicillin is mainly chemisorption. Using the intraparticle diffusion model, the mechanism of the adsorption process was determined. The equilibrium data analysis showed that the Sips and Langmuir models fitted well the experimental data with maximal adsorption capacities of 67.7 and 57 mg/g, respectively, at 25 °C. The chemical-activated carbon of olive stones could be considered as an efficient adsorbent for amoxicillin removal from aqueous solutions.

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. Falling Behind: International Scrutiny of the Peaceful Atom

    Science.gov (United States)

    2008-02-01

    the owner or operator. 3. Reestablish material accountancy as the IAEA’s top safeguards mission by pacing the size and growth in the agency’s...effort, though, is still being implemented at an excruciatingly slow pace due to a lack of funds.18 23 STRUCTURAL PROBLEMS The current gap in the...also at the International School of Nuclear Law, OECD Nuclear Energy Agency and University of Montpellier 1, France. Dr. Michel is also an expert

  17. Catalytic conversion of alcohols having at least three carbon atoms to hydrocarbon blendstock

    Science.gov (United States)

    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.

  18. 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).

  19. Effect of pKa on the kinetics of carbon dioxide absorption in aqueous alkanolamine solutions containing carbonic anhydrase at 298K

    NARCIS (Netherlands)

    Penders-van Elk, Nathalie J M C; Fradette, Sylvie; Versteeg, Geert F.

    2015-01-01

    The absorption of carbon dioxide in various aqueous alkanolamine solutions have been studied with and without carbonic anhydrase respectively in a stirred cell reactor at 298K. The examined alkanolamines were: N,N-diethylethanolamine (DEMEA), N,N-dimethylethanolamine (DMMEA), monoethanolamine (MEA),

  20. 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

  1. 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...... 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....

  2. 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.

  3. ATOMIC FORCE LITHOGRAPHY OF NANO MICROFLUIDIC CHANNELS FOR VERIFICATION AND MONITORING IN AQUEOUS SOLUTIONS

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-06-09

    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.

  4. Electrochemical behavior of metribuzin on a glassy carbon electrode in an aqueous medium including quantitative studies by anodic stripping voltammetry

    OpenAIRE

    Lima,Augusto César de Andrade; Silva,Emanuella Gomes da; Goulart, Marília Oliveira Fonseca; Tonholo, Josealdo; Silva, Tiago Terto da; Abreu,Fabiane Caxico de

    2009-01-01

    The electrochemical behavior of the herbicide metribuzin was studied in an aqueous solution on glassy carbon, carbon paste/Nujol oil and carbon paste/castor oil using cyclic voltammetry, square-wave voltammetry, differential pulse voltammetry, controlled-potential coulometry and electrolysis, for quantification and decontamination purposes. The main electrolytic products obtained from the reduction of metribuzin, after consumption of 8.26 mol electron mol-1, were deaminometribuzin and diketom...

  5. Preconcentration, Separation and Determination of lead(II) with Methyl Thymol Blue Adsorbed on Activated Carbon Using Flame Atomic Absorption Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Ensafi, Ali A.; Ghaderi, Ali R. [Isfahan University of Technology, Isfahan (Iran, Islamic Republic of)

    2008-02-15

    An on-line system for preconcentration and separation of lead(II) is presented. The method is based on the complex formation of Pb(II) with adsorbed Methyl thymol blue on activated carbon. The conditions of preparing the solid phase reagent and of quantitative recovery of Pb(II) from diluted solutions, such as acidity of aqueous phase, solid phase capacity, and flow variables were studied as well as effect of potential interfering ions. After preconcentration step, the metal ions are eluted automatically by 5 ml of 0.5 M HNO{sub 3} solution and the lead ions content was determined by flame atomic absorption spectrometry. Under the optimum conditions, the lead ions in aqueous samples were separated and preconcentrated about 1000-fold by the column. The detection limit was 0.001 μg mL{sup -1}. Lead has been determined in river and tap water samples, with recovery of 98 to 102%.

  6. Constant-distance mode scanning potentiometry. 1. Visualization of calcium carbonate dissolution in aqueous solution.

    Science.gov (United States)

    Etienne, Mathieu; Schulte, Albert; Mann, Stefan; Jordan, Guntram; Dietzel, Irmgard D; Schuhmann, Wolfgang

    2004-07-01

    Constant-distance mode scanning potentiometry was established by integrating potentiometric microsensors as ion-selective scanning probes into a SECM setup that was equipped with a piezoelectric shear force-based tip-to-sample distance control. The combination of specially designed micrometer-sized potentiometric tips with an advanced system for tip positioning allowed simultaneous acquisition of both topographic and potentiometric information at solid/liquid interfaces with high spatial resolution. The performance of the approach was evaluated by applying Ca(2+)-selective constant-distance mode potentiometry to monitor the dissolution of calcium carbonate occurring either at the (104) surface of calcite crystals or in proximity to the more complex surface of cross sections of a calcium carbonate shell of Mya arenaria exposed to slightly acidic aqueous solutions. Micrometer-scale heterogeneities in the apparent calcium activity profiles have successfully been resolved for both samples.

  7. Stable sequestration of single-walled carbon nanotubes in self-assembled aqueous nanopores.

    Science.gov (United States)

    Mauter, Meagan S; Elimelech, Menachem; Osuji, Chinedum O

    2012-03-07

    We demonstrate the ability to stably sequester individual single-walled carbon nanotubes (SWNTs) within self-contained nanometer-scale aqueous volumes arrayed in an organic continuum. Large areal densities of 4 × 10(9) cm(-2) are readily achieved. SWNTs are incorporated into a surfactant mesophase which forms 2.3 nm diameter water channels by lyotropic self-assembly. Near-infrared fluorescence spectroscopy demonstrates that the SWNTs exist as well-dispersed tubes that are stable over several months and through multiple cycles of heating and cooling. Absence of physical distortion of the mesophase suggests that the SWNTs are stabilized by adsorbed surfactants that do not extend considerably from the surface. Our findings have important implications for templated assembly of carbon nanotubes using soft mesophases and the development of functional nanocomposites. © 2012 American Chemical Society

  8. 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.

  9. 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.

  10. The effect of carbon nanotube chirality on the spiral flow of copper atoms in their cores

    Energy Technology Data Exchange (ETDEWEB)

    Lim, M.C.G., E-mail: M070041@e.ntu.edu.sg [Nanyang Technological University, School of Mechanical and Aerospace Engineering, 50 Nanyang Avenue, Singapore 639798 (Singapore); Zhong, Z.W. [Nanyang Technological University, School of Mechanical and Aerospace Engineering, 50 Nanyang Avenue, Singapore 639798 (Singapore)

    2012-12-14

    The effect of carbon nanotube (CNT) chirality on the flow of copper atoms along its core has been investigated using molecular dynamics simulations. The investigation is conducted using CNTs of different chirality, and different flow conditions such as temperatures, bias voltages and the initial positions of the copper atoms. The results show that the atoms flow in a spiral fashion along the CNT channels. The effect is most evident in the CNT channel with zigzag CNTs. The movement of the copper atoms is more erratic when the temperature is increased at a low biased voltage, regardless of the types of channel used. The initial positions of the copper atoms affect the way they converge as they move downstream along the channel. A bias voltage of 4 V favours the initiation of a spiral flow, especially when the position of the copper atoms is far from the central axis of the channel. -- Highlights: Black-Right-Pointing-Pointer We model the transportation of copper atoms in armchair and zigzag CNT channels. Black-Right-Pointing-Pointer The spiral flow of copper atoms occurs in a semiconductor-semiconductor CNT. Black-Right-Pointing-Pointer The compact copper mass is predicted to occur at 673 K with a 4 V bias voltage.

  11. Internal Spin Control, Squeezing and Decoherence in Ensembles of Alkali Atomic Spins

    Science.gov (United States)

    Norris, Leigh Morgan

    Large atomic ensembles interacting with light are one of the most promising platforms for quantum information processing. In the past decade, novel applications for these systems have emerged in quantum communication, quantum computing, and metrology. Essential to all of these applications is the controllability of the atomic ensemble, which is facilitated by a strong coupling between the atoms and light. Non-classical spin squeezed states are a crucial step in attaining greater ensemble control. The degree of entanglement present in these states, furthermore, serves as a benchmark for the strength of the atom-light interaction. Outside the broader context of quantum information processing with atomic ensembles, spin squeezed states have applications in metrology, where their quantum correlations can be harnessed to improve the precision of magnetometers and atomic clocks. This dissertation focuses upon the production of spin squeezed states in large ensembles of cold trapped alkali atoms interacting with optical fields. While most treatments of spin squeezing consider only the case in which the ensemble is composed of two level systems or qubits, we utilize the entire ground manifold of an alkali atom with hyperfine spin f greater than or equal to 1/2, a qudit. Spin squeezing requires non-classical correlations between the constituent atomic spins, which are generated through the atoms' collective coupling to the light. Either through measurement or multiple interactions with the atoms, the light mediates an entangling interaction that produces quantum correlations. Because the spin squeezing treated in this dissertation ultimately originates from the coupling between the light and atoms, conventional approaches of improving this squeezing have focused on increasing the optical density of the ensemble. The greater number of internal degrees of freedom and the controllability of the spin-f ground hyperfine manifold enable novel methods of enhancing squeezing. In

  12. Mercury removal from aqueous solution and flue gas by adsorption on activated carbon fibres

    Science.gov (United States)

    Nabais, João Valente; Carrott, P. J. M.; Carrott, M. M. L. Ribeiro; Belchior, Marisa; Boavida, Dulce; Diall, Tatiana; Gulyurtlu, Ibrahim

    2006-06-01

    The use of two activated carbon fibres, one laboratorial sample prepared from a commercial acrylic textile fibre and one commercial sample of Kynol ®, as prepared/received and modified by reaction with powdered sulfur and H 2S 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 for the mercury uptake is the type of sulfur introduced rather than the total amount and it was found that the H 2S treatment of ACF leads to samples with the highest mercury uptake, despite the lower sulfur amount introduced. The modified samples by both methods can remove HgCl 2 from aqueous solutions at pH 6 within the range 290-710 mg/g (ACF) which can be favourably compared with other studies already published. The use of a filter made with an activated carbon fibre modified by powdered sulfur totally removed the mercury species present in the flue gases produced by combustion of fossil fuel.

  13. Novel Carbon Materials in the Cathode Formulation for High Rate Rechargeable Hybrid Aqueous Batteries

    Directory of Open Access Journals (Sweden)

    Xiao Zhu

    2017-11-01

    Full Text Available Novel carbon materials, carbon nanotubes (CNTs and porous graphene (PG, were exploited and used as conductive additives to improve the rate performance of LiMn2O4 cathode for the rechargeable aqueous Zn/LiMn2O4 battery, namely the rechargeable hybrid aqueous battery (ReHAB. Thanks to the long-range conductivity and stable conductive network provided by CNTs, the rate and cycling performances of LiMn2O4 cathode in ReHAB are highly improved—up to about 100 mAh·g−1 capacity is observed at 10 C (1 C = 120 mAh·g−1. Except for CNTs, porous graphene (PG with a high surface area, an abundant porous structure, and an excellent electrical conductivity facilitates the transportation of Li ions and electrons, which can also obviously enhance the rate capability of the ReHAB. This is important because the ReHAB could be charged/discharged in a few minutes, and this leads to potential application of the ReHAB in automobile industry.

  14. 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.

  15. Precipitation of Co(2+) carbonates from aqueous solution: insights on the amorphous to crystalline transformation.

    Science.gov (United States)

    González-López, Jorge; Fernández-González, Ángeles; Jiménez, Amalia

    2016-04-01

    Cobalt is toxic metal that is present only as a trace in the Earth crust. However, Co might concentrate on specific areas due to both natural and anthropogenic factors and thus, soils and groundwater can be contaminated. It is from this perspective that we are interested in the precipitation of cobalt carbonates, since co-precipitation with minerals phases is a well-known method for metal immobilization in the environment. In particular, the carbonates are widely used due to its reactivity and natural abundance. In order to evaluate the cobalt carbonate precipitation at room temperature, a simple experimental work was carried out in this work. The precipitation occurred via reaction of two common salts: 0.05M of CoCl2 and 0.05M of Na2CO3 in aqueous solution. After reaction, the precipitated solid was kept in the remaining water at 25 oC and under constant stirring for different aging times of 5 min, 1 and 5 hours, 1, 2, 4, 7, 30 and 60 days. In addition to the aging and precipitation experiments, we carried out experiments to determine the solubility of the solids. In these experiments each precipitate was dissolved in Milli-Q water until equilibrium was reached and then the aqueous solution was analyzed regarding Co2+ and total alkalinity. Furthermore, acid solution calorimetry of the products were attained. Finally, we modeled the results using the PHREEQC code. Solid and aqueous phase identification and characterization have been extensively reported in a previous work (González-López et al., 2015). The main results of our investigation were the initial precipitation of an amorphous cobalt carbonate that evolve towards a poorly crystalline cobalt hydroxide carbonate with aging treatment. Solubility of both phases have been calculated under two different approaches: precipitation and dissolution. Values of solubility from each approach were obtained with a general error due to differences in experiment conditions, for instance, ionic strength, temperature and

  16. Probing buried carbon nanotubes within polymer-nanotube composite matrices by Atomic Force Microscopy

    NARCIS (Netherlands)

    Phang, In Yee; Liu, Tianxi; Zhang, Wei-De; Schönherr, Holger; Vancso, Gyula J.

    2007-01-01

    Multi-walled carbon nanotubes (MW-CNT) inside a polyamide-6 (PA6)–MW-CNT composite were visualized by atomic force microscopy (i) in a field-assisted intermittent contact and (ii) in the tunneling (TUNA) mode. Individual buried MW-CNTs were clearly discerned within the PA6 matrix. An average

  17. Noncontact atomic force microscopy in liquid environment with quartz tuning fork and carbon nanotube probe

    DEFF Research Database (Denmark)

    Kageshima, M.; Jensenius, Henriette; Dienwiebel, M.

    2002-01-01

    A force sensor for noncontact atomic force microscopy in liquid environment was developed by combining a multiwalled carbon nanotube (MWNT) probe with a quartz tuning fork. Solvation shells of octamethylcyclotetrasiloxane surface were detected both in the frequency shift and dissipation. Due...

  18. Structural and chemical evolution of single-wall carbon nanotubes under atomic and molecular deuterium interaction

    NARCIS (Netherlands)

    Lisowski, W.F.; Keim, Enrico G.; van den Berg, A.H.J.; Smithers, M.A.; Smithers, Mark A.

    2005-01-01

    The interaction of atomic (D) and molecular (D2) deuterium, as present in a (D + D2) gas mixture, with single-wall carbon nanotubes (SWNTs) has been studied by means of a combination of scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. The SWNT

  19. A comparison of fenuron degradation by hydroxyl and carbonate radicals in aqueous solution.

    Science.gov (United States)

    Mazellier, Patrick; Busset, Cécile; Delmont, Anne; De Laat, Joseph

    2007-12-01

    A comparative study of the transformation of the herbicide fenuron (1,1-dimethyl-3-phenylurea) by hydroxyl radicals and carbonate radicals in aqueous solution (pH 7.2-phosphate buffer) has been undertaken. Hydroxyl radical was generated by the well-known photolysis of hydrogen peroxide at 254 nm and carbonate radical was formed by photolysis of Co(NH(3))(5)CO(3)(+) at 254 nm. Competitive kinetic experiments were performed with atrazine used as the main competitor for both processes. Accordingly, the second-order rate constant of reaction between fenuron and carbonate radical was found to be (7-12+/-3)x10(6)M(-1)s(-1) [(7+/-1)x10(9)M(-1)s(-1) for hydroxyl radical]. The formation of degradation products was studied by LC-MS in the two cases and a comparison has been performed. The reaction with carbonate radical leads to the formation of a quinone-imine derivative which appears as the major primary product together with ortho and para hydroxylated compounds. These two compounds represent the major products in the reaction with hydroxyl radicals. The reaction of both radicals also leads to the transformation of the dimethylurea moiety.

  20. Spatial Distributions of Metal Atoms During Carbon SWNTs Formation: Measurements and Modelling

    Science.gov (United States)

    Cau, M.; Dorval, N.; Attal-Tretout, B.; Cochon, J. L.; Loiseau, A.; Farhat, S.; Hinkov, I.; Scott, C. D.

    2004-01-01

    Experiments and modelling have been undertaken to clarify the role of metal catalysts during single-wall carbon nanotube formation. For instance, we wonder whether the metal catalyst is active as an atom, a cluster, a liquid or solid nanoparticle [1]. A reactor has been developed for synthesis by continuous CO2-laser vaporisation of a carbon-nickel-cobalt target in laminar helium flow. The laser induced fluorescence technique [2] is applied for local probing of gaseous Ni, Co and CZ species throughout the hot carbon flow of the target heated up to 3500 K. A rapid depletion of C2 in contrast to the spatial extent of metal atoms is observed in the plume (Fig. 1). This asserts that C2 condenses earlier than Ni and Co atoms.[3, 4]. The depletion is even faster when catalysts are present. It may indicate that an interaction between metal atoms and carbon dimers takes place in the gas as soon as they are expelled from the target surface. Two methods of modelling are used: a spatially I-D calculation developed originally for the arc process [5], and a zero-D time dependent calculation, solving the chemical kinetics along the streamlines [6]. The latter includes Ni cluster formation. The peak of C2 density is calculated close to the target surface where the temperature is the highest. In the hot region, C; is dominant. As the carbon products move away from the target and mix with the ambient helium, they recombine into larger clusters, as demonstrated by the peak of C5 density around 1 mm. The profile of Ni-atom density compares fairly well with the measured one (Fig. 2). The early increase is due to the drop of temperature, and the final decrease beyond 6 mm results from Ni cluster formation at the eutectic temperature (approx.1600 K).

  1. 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.

  2. Removal of Dissolved Organic Carbon from aqueous solution by Fenton Oxidation Process

    Directory of Open Access Journals (Sweden)

    Hamed Biglari

    2012-05-01

    Full Text Available Background and Aim: Nowadays, regarding the increased human and geological activities, concentrations of toxic and carcinogenic disinfectant by-products– like Trihalomethanes -which have an organic base, in drinking water sources, has worryingly increased. Thus, the present study aimed at surveying the amount of dissolved organic carbon (doc removed from aqueous solution by Fenton process. Materials and Methods: In this descriptive study, the outcome of removing dissolved organic carbon derived from natural water with initial concentrations 2, 4, and 8 mg/l using one-liter water containers by means of Fenton Process at PHs 2, 3, 4, and 5 due to adding 20, 40, 60, and 80 mg/l of H2O2 and Ferrous ions with 4, 8, 12, and 16 mg/l concentrations at oxidation time 5, 10, 20, and 40 minutes was calculated. Finally, the outcome of carbon removal was assessed by means of TOC analyzer. Results: It was found that the most outcome of dissolved organic carbon removal (about 97% belonged to 10/1 H2O2 and Ferrous ion , while dissolved organic carbon PH was 3 and its initial concentration was 2mg/l and oxidation time was 40 minutes. Conclusion: Generally speaking, it was confirmed that the improved Fenton Oxidation Process can efficiently be used to refine water containing dissolved organic carbon. The method was found to be highly and relatively fast compared to conventional existing techniques and also, it can be concluded that the Fenton process has the potential to be utilized for the cost-effective removal of DOC from water and wastewater.

  3. 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

  4. A new material with atomized cobalt-multiwalled carbon nanotubes: a possible substitute for human implants.

    Science.gov (United States)

    Joshi, Bharat; Gupta, Sachin; Kalra, Nitin; Gudyka, Russell; Santhanam, K S V

    2010-06-01

    A new material composed of atomized cobalt-multiwalled carbon nanotube has been produced and characterized by thermogravimetric analysis and polarization studies to estimate its lifetime. This does not show cobalt thermal oxidation suggesting that it is confined inside the carbon nanotube matrix. The density functional calculations in the literature predict a strong interaction leading to higher hybridization of cobalt atom and carbon nanotubes. A detailed investigation of the corrosion measurements shows that the new material of thickness 0.8 mm, 1 mm, 1.5 mm and 2 mm would last for 31, 39, 60 and 79 years and it would substitute with cobalt-chromium alloy that is used as a load bearing implant for patients with knee pain or partial denture implant.

  5. 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

  6. 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.

  7. 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

  8. 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...

  9. Characterization of local hydrophobicity on sapphire (0001) surfaces in aqueous environment by colloidal probe atomic force microscopy

    Science.gov (United States)

    Wada, Tomoya; Yamazaki, Kenji; Isono, Toshinari; Ogino, Toshio

    2017-02-01

    Sapphire (0001) surfaces exhibit a phase-separation into hydrophobic and hydrophilic domains upon high-temperature annealing, which were previously distinguished by the thickness of adsorbed water layers in air using atomic force microscopy (AFM). To characterize their local surface hydrophobicity in aqueous environment, we used AFM equipped with a colloidal probe and measured the local adhesive force between each sapphire domain and a hydrophilic SiO2 probe surface, or a hydrophobic polystyrene one. Two data acquisition modes for statistical analyses were used: one is force measurements at different positions of the surface and the other repeated measurement at a fixed position. We found that adhesive force measurements using the polystyrene probe allow us to distinctly separate the hydrophilic and hydrophobic domains. The dispersion in the force measurement data at different positions of the surface is larger than that in the repeated measurements at a fixed position. It indicates that the adhesive force measurement is repeatable although their data dispersion for the measurement positions is relatively large. From these results, we can conclude that the hydrophilic and hydrophobic domains on the sapphire (0001) surfaces are distinguished by a difference in their hydration degrees.

  10. 76 FR 58049 - Atomic Safety and Licensing Board; Honeywell International, Inc.; Metropolis Works Uranium...

    Science.gov (United States)

    2011-09-19

    ... 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, 74... Financial Assurance Requirements, Honeywell Metropolis Works, Material License No. SUB- 526 (TAC No. L32718...

  11. 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.

  12. 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.

  13. Silicon solar cell performance deposited by diamond like carbon thin film ;Atomic oxygen effects;

    Science.gov (United States)

    Aghaei, Abbas Ail; Eshaghi, Akbar; Karami, Esmaeil

    2017-09-01

    In this research, a diamond-like carbon thin film was deposited on p-type polycrystalline silicon solar cell via plasma-enhanced chemical vapor deposition method by using methane and hydrogen gases. The effect of atomic oxygen on the functioning of silicon coated DLC thin film and silicon was investigated. Raman spectroscopy, field emission scanning electron microscopy, atomic force microscopy and attenuated total reflection-Fourier transform infrared spectroscopy were used to characterize the structure and morphology of the DLC thin film. Photocurrent-voltage characteristics of the silicon solar cell were carried out using a solar simulator. The results showed that atomic oxygen exposure induced the including oxidation, structural changes, cross-linking reactions and bond breaking of the DLC film; thus reducing the optical properties. The photocurrent-voltage characteristics showed that although the properties of the fabricated thin film were decreased after being exposed to destructive rays, when compared with solar cell without any coating, it could protect it in atomic oxygen condition enhancing solar cell efficiency up to 12%. Thus, it can be said that diamond-like carbon thin layer protect the solar cell against atomic oxygen exposure.

  14. Facile synthesis of analogous graphene quantum dots with sp2 hybridized carbon atom dominant structures and their photovoltaic application

    Science.gov (United States)

    Huang, Zhengcheng; Shen, Yongtao; Li, Yu; Zheng, Wenjun; Xue, Yunjia; Qin, Chengqun; Zhang, Bo; Hao, Jingxiang; Feng, Wei

    2014-10-01

    Graphene quantum dot (GQD) is an emerging class of zero-dimensional nanocarbon material with many novel applications. It is of scientific importance to prepare GQDs with more perfect structures, that is, GQDs containing negligible oxygenous defects, for both optimizing their optical properties and helping in their photovoltaic applications. Herein, a new strategy for the facile preparation of ``pristine'' GQDs is reported. The method we presented is a combination of a bottom-up synthetic and a solvent-induced interface separation process, during which the target products with highly crystalline structure were selected by the organic solvent. The obtained organic soluble GQDs (O-GQDs) showed a significant difference in structure and composition compared with ordinary aqueous soluble GQDs, thus leading to a series of novel properties. Furthermore, O-GQDs were applied as electron-acceptors in a poly(3-hexylthiophene) (P3HT)-based organic photovoltaic device. The performance highlights that O-GQD has potential to be a novel electron-acceptor material due to the sp2 hybridized carbon atom dominant structure and good solubility in organic solvents.Graphene quantum dot (GQD) is an emerging class of zero-dimensional nanocarbon material with many novel applications. It is of scientific importance to prepare GQDs with more perfect structures, that is, GQDs containing negligible oxygenous defects, for both optimizing their optical properties and helping in their photovoltaic applications. Herein, a new strategy for the facile preparation of ``pristine'' GQDs is reported. The method we presented is a combination of a bottom-up synthetic and a solvent-induced interface separation process, during which the target products with highly crystalline structure were selected by the organic solvent. The obtained organic soluble GQDs (O-GQDs) showed a significant difference in structure and composition compared with ordinary aqueous soluble GQDs, thus leading to a series of novel

  15. 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.

  16. Theoretical realization of cluster-assembled hydrogen storage materials based on terminated carbon atomic chains.

    Science.gov (United States)

    Liu, Chun-Sheng; An, Hui; Guo, Ling-Ju; Zeng, Zhi; Ju, Xin

    2011-01-14

    The capacity of carbon atomic chains with different terminations for hydrogen storage is studied using first-principles density functional theory calculations. Unlike the physisorption of H(2) on the H-terminated chain, we show that two Li (Na) atoms each capping one end of the odd- or even-numbered carbon chain can hold ten H(2) molecules with optimal binding energies for room temperature storage. The hybridization of the Li 2p states with the H(2)σ orbitals contributes to the H(2) adsorption. However, the binding mechanism of the H(2) molecules on Na arises only from the polarization interaction between the charged Na atom and the H(2). Interestingly, additional H(2) molecules can be bound to the carbon atoms at the chain ends due to the charge transfer between Li 2s2p (Na 3s) and C 2p states. More importantly, dimerization of these isolated metal-capped chains does not affect the hydrogen binding energy significantly. In addition, a single chain can be stabilized effectively by the C(60) fullerenes termination. With a hydrogen uptake of ∼10 wt.% on Li-coated C(60)-C(n)-C(60) (n = 5, 8), the Li(12)C(60)-C(n)-Li(12)C(60) complex, keeping the number of adsorbed H(2) molecules per Li and stabilizing the dispersion of individual Li atoms, can serve as better building blocks of polymers than the (Li(12)C(60))(2) dimer. These findings suggest a new route to design cluster-assembled hydrogen storage materials based on terminated sp carbon chains.

  17. Adsorption of malachite green from aqueous solution onto carbon prepared from Arundo donax root

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Jian [School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China)], E-mail: zhangjian00@sdu.edu.cn; Li Yan; Zhang Chenglu; Jing Yuming [School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China)

    2008-02-11

    Arundo donax root carbon (ADRC), a new adsorbent, was prepared from Arundo donax root by carbonization. The surface area of the adsorbent was determined 158 m{sup 2}/g by N{sub 2} adsorption isotherm. Batch adsorption experiments were carried out for the removal of malachite green (MG) from aqueous solution using ADRC as adsorbent. The effects of various parameters such as solution pH (3-10), carbon dose (0.15-1.0 g/100 ml) and initial MG concentration (10-100 mg/l) on the adsorption system were investigated. The effective pH was 5-7 and the optimum adsorbent dose was found to be 0.6 g/100 ml. Equilibrium experimental data at 293, 303 and 313 K were better represented by Langmuir isotherm than Freundlich isotherm using linear and non-linear methods. Thermodynamic parameters such as {delta}G, {delta}H and {delta}S were also calculated. The negative Gibbs free energy change and the positive enthalpy change indicated the spontaneous and endothermic nature of the adsorption. The adsorption equilibrium time was 180 min. Adsorption kinetics was determined using pseudo-first-order model, pseudo-second-order model and intraparticle diffusion model. The results showed that the adsorption of MG onto ADRC followed pseudo-second-order model.

  18. Preparation of Multiwalled Carbon Nanotube-Poly (4-Styrenesulfonic Acid Aqueous Dispersion for Dopamine Sensing

    Directory of Open Access Journals (Sweden)

    Aihua LIU

    2006-12-01

    Full Text Available A simple and facile method for the non-covalent functionalization of multi-walled carbon nanotubes (MWNTs using poly(4-styrenesulfonic acid (PSS is proposed. The resulting PSS-MWNTs dispersion is readily soluble in water and can be left to stand for 2 weeks at room temperature, no phase separation with aggregation of nanotubes at the bottom of the vials was observed. The as-prepared PSS-MWNTs dispersions could facilitate the processing of the nanotubes into composites with high nanotube loading. The PSS-MWNTs complex shows high electrocatalytic activity to the oxidation of neutrontransmitter of dopamine, suggesting that the coating of PSS onto carbon nanotubes surface without destroying the electronic structures of the pristine carbon nanotubes; therefore, the unique properties including the catalytic property of the nanotubes retained. It is envisioned that the PSS-MWNTs aqueous dispersions may find possible applications in the development of biosensors, bioelectronics, separation and environment protection as well as other biological events where water-based environment is required.

  19. 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.

  20. Application of a novel magnetic carbon nanotube adsorbent for removal of mercury from aqueous solutions.

    Science.gov (United States)

    Homayoon, Farshid; Faghihian, Hossein; Torki, Firoozeh

    2017-04-01

    In this research, multiwall carbon nanotube was magnetized and subsequently functionalized by thiosemicarbazide. After characterization by FTIR, BET, SEM, EDAX, and VSM techniques, the magnetized adsorbent (multi-walled carbon nanotubes (MWCNTs)/Fe3O4) was used for removal of Hg(2+) from aqueous solutions and the experimental conditions were optimized. The adsorption capacity of 172.83 mg g(-1) was obtained at 25 °C and pH = 3 which was superior to the value obtained for initial multiwall carbon nanotube, magnetized sample, and many previously reported values. In the presence of Pb(+2) and Cd(+2), the adsorbent was selective towards mercury when their concentration was respectively below 50 and 100 mg L(-1). The adsorption process was kinetically fast and the equilibration was attained within 60 min with 69.5% of the capacity obtained within 10 min. The used adsorbent was regenerated by HNO3 solution, and the regenerated adsorbent retained 92% of its initial capacity. The magnetic sensitivity of the adsorbent allowed the simple separation of the used adsorbent from the solution by implying an appropriate external magnetic field. The adsorption data was well fitted to the Langmuir isotherm model, indicating homogeneous and monolayer adsorption of mercury by the adsorbent.

  1. [Determination of low-carbon alcohols, aldehydes and ketones in aqueous products of Fischer-Tropsch synthesis by gas chromatography].

    Science.gov (United States)

    Gai, Qingqing; Wu, Peng; Shi, Yulin; Bai, Yu; Long, Yinhua

    2015-01-01

    A method for the determination of low-carbon (C1-C8) alcohols, aldehydes and ketones in aqueous products of Fischer-Tropsch synthesis was developed by gas chromatography. It included the optimization of separation conditions, the precision and accuracy of determination, and the use of correction factors of the analytes to ethanol for quantification. The aqueous products showed that the correlation coefficients for ethanol in different content ranges were above 0.99, which means it had good linear correlations. The spiked recoveries in the aqueous samples of Fischer-Tropsch synthesis were from 93.4% to 109.6%. The accuracy of the method can satisfy the requirement for the analysis of the aqueous samples of Fischer-Tropsch synthesis. The results showed that the total mass fractions of the major low-carbon alcohols, aldehydes, ketones in aqueous products of Fischer-Tropsch synthesis were about 3%-12%, and the contents of ethanol were the highest (about 1.7%-7.3%). The largest share of the total proportion was n-alcohols, followed by isomeric alcohols, aldehydes and ketones were the lowest. This method is simple, fast, and has great significance for the analysis of important components in aqueous products of Fischer-Tropsch synthesis.

  2. 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.

  3. Recent Advances in Atomic Metal Doping of Carbon-based Nanomaterials for Energy Conversion.

    Science.gov (United States)

    Bayatsarmadi, Bita; Zheng, Yao; Vasileff, Anthony; Qiao, Shi-Zhang

    2017-06-01

    Nanostructured metal-contained catalysts are one of the most widely used types of catalysts applied to facilitate some of sluggish electrochemical reactions. However, the high activity of these catalysts cannot be sustained over a variety of pH ranges. In an effort to develop highly active and stable metal-contained catalysts, various approaches have been pursued with an emphasis on metal particle size reduction and doping on carbon-based supports. These techniques enhances the metal-support interactions, originating from the chemical bonding effect between the metal dopants and carbon support and the associated interface, as well as the charge transfer between the atomic metal species and carbon framework. This provides an opportunity to tune the well-defined metal active centers and optimize their activity, selectivity and stability of this type of (electro)catalyst. Herein, recent advances in synthesis strategies, characterization and catalytic performance of single atom metal dopants on carbon-based nanomaterials are highlighted with attempts to understand the electronic structure and spatial arrangement of individual atoms as well as their interaction with the supports. Applications of these new materials in a wide range of potential electrocatalytic processes in renewable energy conversion systems are also discussed with emphasis on future directions in this active field of research. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Adsorption Sites of Hydrogen Atom on Pure and Mg-Doped Multi-Walled Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    A. A. Al-Ghamdi

    2012-01-01

    Full Text Available Hydrogen adsorption sites on pure multiwalled carbon nanotube (MWCNT and Mg-doped MWCNTs material system have been investigated using molecular dynamics (MD simulations as well as quantum chemical calculations. Through combining MWCNTs with Mg, the hydrogen adsorption sites energy on this Mg-MWCNTs system is found to be larger than that of the pure MWCNTs. Additionally, it was found that, through Mg-doping, new adsorption sites for hydrogen molecules are created in comparison with undoped nanotubes. It is also found that H atom is preferably adsorbed at every place near magnesium atom.

  5. Kinetics and mechanism of carbamate formation from CO2(aq), carbonate species, and monoethanolamine in aqueous solution.

    Science.gov (United States)

    McCann, Nichola; Phan, Duong; Wang, Xiaoguang; Conway, William; Burns, Robert; Attalla, Moetaz; Puxty, Graeme; Maeder, Marcel

    2009-04-30

    Removal of carbon dioxide from fossil-based power generation is a potentially useful technique for the reduction of greenhouse gas emissions. Reversible interaction with aqueous amine solutions is most promising. In this process, the formation of carbamates is an important reaction of carbon dioxide. In this contribution, a detailed molecular reaction mechanism for the carbamate formation between MEA (monoethanolamine) and dissolved CO(2) as well as carbonate species in aqueous solution is presented. There are three parallel, reversible reactions of the free amine with CO(2), carbonic acid, and the bicarbonate ion; the relative importance of the three paths is strongly pH dependent. Kinetic and equilibrium measurements are based on (1)H NMR and stopped-flow measurements with rate constants, equilibrium constants, and protonation constants being reported.

  6. Influence of internal composition on physicochemical properties of alginate aqueous-core capsules.

    Science.gov (United States)

    Ben Messaoud, Ghazi; Sánchez-González, Laura; Probst, Laurent; Desobry, Stéphane

    2016-05-01

    To enhance physicochemical properties of alginate aqueous-core capsules, conventional strategies were focused in literature on designing composite and coated capsules. In the present study, own effect of liquid-core composition on mechanical and release properties was investigated. Capsules were prepared by dripping a CaCl2 solution into an alginate gelling solution. Viscosity of CaCl2 solution was adjusted by adding cationic, anionic and non-ionic naturally derived polymers, respectively chitosan, xanthan gum and guar gum. In parallel, uniform alginate hydrogels were prepared by different methods (pouring, in situ forming and mixing). Mechanical stability of capsules and plane hydrogels were respectively evaluated by compression experiments and small amplitude oscillatory shear rheology and then correlated. Capsules permeability was evaluated by monitoring diffusion of encapsulated cochineal dye, riboflavin and BSA. The core-shell interactions were investigated by ATR-FTIR. Results showed that inner polymer had an impact on membrane stability and could act as an internal coating or provide mechanical reinforcement. Mechanical properties of alginate capsules were in a good agreement with rheological behavior of plane hydrogels. Release behavior of the entrapped molecules changed considerably. This study demonstrated the importance of aqueous-core composition, and gave new insights for possible adjusting of microcapsules physicochemical properties by modulating core-shell interactions. Copyright © 2016 Elsevier Inc. All rights reserved.

  7. The International Atomic Energy Agency's activities in radiation medicine and cancer: promoting global health through diplomacy.

    Science.gov (United States)

    Deatsch-Kratochvil, Amanda N; Pascual, Thomas Neil; Kesner, Adam; Rosenblatt, Eduardo; Chhem, Rethy K

    2013-02-01

    Global health has been an issue of seemingly low political importance in comparison with issues that have direct bearing on countries' national security. Recently, health has experienced a "political revolution" or a rise in political importance. Today, we face substantial global health challenges, from the spread of infectious disease, gaps in basic maternal and child health care, to the globalization of cancer. A recent estimate states that the "overall lifetime risk of developing cancer (both sexes) is expected to rise from more than one in three to one in two by 2015." These issues pose significant threats to international health security. To successfully combat these grave challenges, the international community must embrace and engage in global health diplomacy, defined by scholars Thomas Novotny and Vicanne Adams as a political activity aimed at improving global health, while at the same time maintaining and strengthening international relations. The IAEA (International Atomic Energy Agency) is an international organization with a unique mandate to "accelerate and enlarge the contribution of atomic energy to peace, health, and prosperity throughout the world." This article discusses global health diplomacy, reviews the IAEA's program activities in human health by focusing on radiation medicine and cancer, and the peaceful applications of atomic energy within the context of global health diplomacy. Copyright © 2013 Canadian Association of Radiologists. Published by Elsevier Inc. All rights reserved.

  8. Energy band alignment and electronic states of amorphous carbon surfaces in vacuo and in aqueous environment

    Energy Technology Data Exchange (ETDEWEB)

    Caro, Miguel A., E-mail: mcaroba@gmail.com [Department of Electrical Engineering and Automation, Aalto University, Espoo (Finland); Department of Applied Physics, COMP Centre of Excellence in Computational Nanoscience, Aalto University, Espoo (Finland); Määttä, Jukka [Department of Chemistry, Aalto University, Espoo (Finland); Lopez-Acevedo, Olga [Department of Applied Physics, COMP Centre of Excellence in Computational Nanoscience, Aalto University, Espoo (Finland); Laurila, Tomi [Department of Electrical Engineering and Automation, Aalto University, Espoo (Finland)

    2015-01-21

    In this paper, we obtain the energy band positions of amorphous carbon (a–C) surfaces in vacuum and in aqueous environment. The calculations are performed using a combination of (i) classical molecular dynamics (MD), (ii) Kohn-Sham density functional theory with the Perdew-Burke-Ernzerhof (PBE) exchange-correlation functional, and (iii) the screened-exchange hybrid functional of Heyd, Scuseria, and Ernzerhof (HSE). PBE allows an accurate generation of a-C and the evaluation of the local electrostatic potential in the a-C/water system, HSE yields an improved description of energetic positions which is critical in this case, and classical MD enables a computationally affordable description of water. Our explicit calculation shows that, both in vacuo and in aqueous environment, the a-C electronic states available in the region comprised between the H{sub 2}/H{sub 2}O and O{sub 2}/H{sub 2}O levels of water correspond to both occupied and unoccupied states within the a-C pseudogap region. These are localized states associated to sp{sup 2} sites in a-C. The band realignment induces a shift of approximately 300 meV of the a-C energy band positions with respect to the redox levels of water.

  9. An Aqueous Metal-ion Capacitor with Oxidised Carbon Nanotubes and Metallic Zinc Electrodes

    Directory of Open Access Journals (Sweden)

    Yuheng Tian

    2016-10-01

    Full Text Available An aqueous metal ion capacitor comprising of a zinc anode, an oxidized carbon nanotubes (oCNTs cathode and a zinc sulfate electrolyte is reported. Since the shuttling cation is Zn2+, this typical metal ion capacitor is named as zinc-ion capacitor (ZIC. The ZIC integrates the divalent zinc stripping/plating chemistry with the surface-enabled pseudocapacitive cation adsorption/desorption on oCNTs. The surface chemistry and crystallographic structure of oCNTs were extensively characterized by combining X-ray photoelectron spectroscopy, Fourier-transformed infrared spectroscopy, Raman spectroscopy and X-ray powder diffraction. The function of the surface oxygen groups in surface cation storage was elucidated by a series of electrochemical measurement and the surface-enabled ZIC showed better performance than the ZIC with an un-oxidized CNT cathode. The reaction mechanism at the oCNT cathode involves the additional reversible Faradaic process, while the CNTs merely show electric double layer capacitive behavior involving a non-Faradaic process. The aqueous hybrid ZIC comprising the oCNT cathode exhibited a specific capacitance of 20 mF cm-2 (corresponding to 53 F g-1 in the range of 0-1.8 V at 10 mV s-1 and a stable cycling performance up to 5000 cycles.

  10. Removal of potentially toxic elements from aqueous solutions and industrial wastewater using activated carbon.

    Science.gov (United States)

    Sajjad, Muhammad; Khan, Sardar; Ali Baig, Shams; Munir, Saduf; Naz, Alia; Ahmad, Sheikh Saeed; Khan, Anwarzeb

    2017-06-01

    Water contamination with potentially toxic elements (PTEs) has become one of the key issues in recent years that threatens human health and ecological systems. The present study is aimed at removing PTEs like cadmium (Cd), chromium (Cr), copper (Cu) and lead (Pb) from aqueous solutions and industrial wastewater using activated carbon (AC) as an adsorbent through different batch and column experiments. Results demonstrated that the removal of PTEs from aqueous solutions was highly pH dependent, except for Cr, and the maximum removal (>78%) was recorded at pH 6.0. However, maximum Cr removal (82.8%) was observed at pH 3.0. The adsorption reached equilibrium after 60 min with 2 g of adsorbent. Coefficient (R 2 ) values suggested by the Langmuir isotherm model were 0.97, 0.96, 0.93 and 0.95 for Cd, Cr, Cu and Pb, respectively, indicating the fit to this model. In column experiments, the maximum removal of PTEs was observed at an adsorbent bed height of 20 cm with the optimal flow rate of 3.56 mL/min. Furthermore, PTEs removal by AC was observed in the order of Cu > Cd > Pb > Cr. Findings from this study suggest that AC could be used as a promising adsorbent for simultaneously removing several PTEs from wastewaters.

  11. Poly (vinylsulfonic acid) assisted synthesis of aqueous solution stable vaterite calcium carbonate nanoparticles.

    Science.gov (United States)

    Nagaraja, Ashvin T; Pradhan, Sulolit; McShane, Michael J

    2014-03-15

    Calcium carbonate nanoparticles of the vaterite polymorph were synthesized by combining CaCl2 and Na2CO3 in the presence of poly (vinylsulfonic acid) (PVSA). By studying the important experimental parameters we found that controlling PVSA concentration, reaction temperature, and order of reagent addition the particle size, monodispersity, and surface charge can be controlled. By increasing PVSA concentration or by decreasing temperature CCNPs with an average size from ≈150 to 500 nm could be produced. We believe the incorporation of PVSA into the reaction plays a dual role to (1) slow down the nucleation rate by sequestering calcium and to (2) stabilize the resulting CCNPs as the vaterite polymorph, preventing surface calcification or aggregation into microparticles. The obtained vaterite nanoparticles were found to maintain their crystal structure and surface charge after storage in aqueous buffer for at least 5 months. The aqueous stable vaterite nanoparticles could be a useful platform for the encapsulation of a large variety of biomolecules for drug delivery or as a sacrificial template toward capsule formation for biosensor applications. Copyright © 2013 Elsevier Inc. All rights reserved.

  12. 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)

  13. 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.

  14. Aqueous suspension methods of carbon-based nanomaterials and biological effects on model aquatic organisms.

    Science.gov (United States)

    Gao, Jie; Llaneza, Veronica; Youn, Sejin; Silvera-Batista, Carlos A; Ziegler, Kirk J; Bonzongo, Jean-Claude J

    2012-01-01

    The preparation of aqueous suspensions of carbon-based nanomaterials (NMs) requires the use of dispersing agents to overcome their hydrophobic character. Although studies on the toxicity of NMs have focused primarily on linking the characteristics of particles to biological responses, the role of dispersing agents has been overlooked. This study assessed the biological effects of a number of commonly used dispersing agents on Pseudokirchneriella subcapitata and Ceriodaphnia dubia as model test organisms. The results show that for a given organism, NM toxicity can be mitigated by use of nontoxic surfactants, and that a multispecies approach is necessary to account for the sensitivity of different organisms. In addition to the intrinsic physicochemical properties of NMs, exposure studies should take into account the effects of used dispersing fluids. Copyright © 2011 SETAC.

  15. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Rais, E-mail: olifiaraju@gmail.com [Environmental Research Laboratory, Department of Applied Chemistry, Aligarh Muslim University, Aligarh, U.P. 202002 (India); Kumar, Rajeev [Environmental Research Laboratory, Department of Applied Chemistry, Aligarh Muslim University, Aligarh, U.P. 202002 (India)

    2010-12-15

    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 {Delta}H{sup o} value of 13.613 kJ/mol.

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

    Science.gov (United States)

    Ahmad, Rais; Kumar, Rajeev

    2010-12-01

    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 Δ H° value of 13.613 kJ/mol.

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

    Energy Technology Data Exchange (ETDEWEB)

    Wang, S.W.

    1980-06-01

    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 313/sup 0/K. Three bi-solute acid mixtures (acetic and propionic acids, acetic and butanoic acids, and propionic and butanoic acids) were studied at 278 and 298/sup 0/K. 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.

  19. Absorption of carbon dioxide in aqueous solutions of imidazolium ionic liquids with carboxylate anions

    Energy Technology Data Exchange (ETDEWEB)

    Baj, Stefan; Krawczyk, Tomasz; Dabrowska, Aleksandra; Siewniak, Agnieszka [Silesian University of Technology, Gliwice (Poland); Sobolewski, Aleksander [Institute for Chemical Processing of Coal, Zabrze (Poland)

    2015-11-15

    The solubility of carbon dioxide at atmospheric pressure in aqueous mixtures of 1,3-alkyl substituted imidazolium ionic liquids (ILs) containing carboxylic anions was studied. The ILs showed increased solubility of CO{sub 2} with decreasing water concentration. The relationship between the CO{sub 2} concentration in solution and the mole fraction of water in the ILs describes a sigmoidal curve. The regression constants of a logistic function were used to quantitatively assess the absorbent capacity and the effect of water on CO{sub 2} absorption. ILs containing the most basic anions, such as pivalate, propionate and acetate, had the best properties. It was observed that the impact of water on absorption primarily depended on the cation structure. The best absorption performance was observed for 1,3-dibutylimidazolium pivalate and 1-butyl-3-methyl imidazolium acetate.

  20. Recovery of glycols, sugars, and Related Multiple -OH Compounds from Dilute-Aqueous Solution by Regenerable Adsorption onto Activated Carbons

    Energy Technology Data Exchange (ETDEWEB)

    Chinn, Daniel [Univ. of California, Berkeley, CA (United States)

    1999-06-01

    The present research explores the use of adsorption onto activated carbons as a means of recover glycerol, glycols, and sugars from dilute-aqueous solution. Our work is focused on understanding the mechanisms of adsorption onto carbons, assessing the degree of adsorption reversibility with precision, and implementing a bench-scale recovery process that results in a higher product concentration and reduction of the energy load for final purification.

  1. Kinetic Approach for the Adsorption of Organophosphorous Pesticides from Aqueous Solution Using “Waste” Jute Fiber Carbon

    OpenAIRE

    Senthilkumaar, S.; Krishna, S. K.; Kalaamanic, P.; Subburamaan, C. V.; N. Ganapathy Subramaniam; Kang, T W

    2010-01-01

    Chemically activated “Waste” Jute Fiber carbon has been effectively used for the removal of five organophosphorous pesticides (malathion, monocrotophos, methylparathion, phosphamidon and dimethoate) from aqueous solutions. The prepared activated jute fiber carbon was characterized by using Elemental analyzer and proximate analysis methods. The adsorption equilibrium was examined at 28 ºC. Three different kinetic models, the pseudo first order, pseudo second order and Elovich kinetic models we...

  2. 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.

  3. AUSTRALIAN PINE CONES-BASED ACTIVATED CARBON FOR ADSORPTION OF COPPER IN AQUEOUS SOLUTION

    Directory of Open Access Journals (Sweden)

    MUSLIM A.

    2017-02-01

    Full Text Available The Australian Pine cones (APCs was utilised as adsorbent material by physical and chemical activation for the adsorption Cu(II in aqueous solution. FTIR and SEM analysis were conducted to obtain the active site and to characterise the surface morphology of the APCs activated carbon (APCs AC prepared through pyrolysis at 1073.15 K and alkaline activation of NaOH. The independent variables effect such as contact time, Cu(II initial concentration and the activator ratio in the ranges of 0-150 min, 84.88-370.21 mg/l and 0.2-0.6 (NaOH:APCs AC, respectively on the Cu(II adsorption capacity were investigated in the APCs activated carbon-solution (APCs ACS system with 1 g the APCs AC in 100 mL Cu(II aqueous solution with magnetic stirring at 75 rpm, room temperature of 298.15 K (± 2 K, 1 atm and pH 5 (±0.25. As the results, Cu(II adsorption capacity dramatically increased with increasing contact time and Cu(II initial concentration. The optimal Cu(II adsorption capacity of 26.71 mg/g was obtained in the APCs ACS system with 120-min contact time, 340.81 m/l initial Cu(II and 0.6 activator ratio. The kinetics study showed the Cu(II adsorption kinetics followed the pseudo-second-order kinetics with 27.03 mg/g of adsorption capacity, 0.09 g/mg.min of rate constant and 0.985-R2. In addition, the Cu(II adsorption isotherm followed the Langmuir model with 12.82 mg/g of the mono-layer adsorption capacity, 42.93 l/g of the over-all adsorption capacity and 0.954-R2.

  4. Adsorption of Cu2+ Ions From Aqueous Solutions Using Oxidized Multi-Walled Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Soheil Sobhanardakani

    2015-06-01

    Full Text Available Copper ion (Cu2+ is one of the heavy metal ions that cause environmental pollution specifically in water. Copper ion cations are not biodegradable and tend to cumulate in living organisms. Consequently, the removal of Cu2+ in environmental samples plays an important role in environmental pollution monitoring. The purpose of the present work was to prepare oxidized Multi-Walled Carbon Nano Tubes (MWCNTs for removal of Cu2+ ions from aqueous solutions. This study was conducted under laboratory conditions. Multi-Walled Carbon Nano Tubes were oxidized and characterized by Fourier Transform Infrared Spectroscopy (FTIR, Scanning Electron Microscope (SEM and the Brunauer, Emmett, and Teller (BET methods. The effects of various factors, such as solution pH (3 - 9, adsorbent dose (0.006 - 0.06 g and contact time (10 - 120 minutes were investigated. Results showed that the suitable pH for Cu2+ ions removal was about 6.0, and the optimal dose was 0.03 g. Isotherm studies indicated that the Langmuir model fits the experimental data better than the Freundlich model. Maximum Cu2+ adsorption capacity was calculated as 200 mg g-1. The kinetics of the adsorption process was tested for the pseudo-first-order and pseudo-second-order models. The comparison among the models showed that the pseudo-second order model best described the adsorption kinetics. The results showed that oxidized MWCNTs can be used as a low cost adsorbent for the removal of Cu2+ ions from aqueous solutions.

  5. A Molecular Dynamics of Cold Neutral Atoms Captured by Carbon Nanotube Under Electric Field and Thermal Effect as a Selective Atoms Sensor.

    Science.gov (United States)

    Santos, Elson C; Neto, Abel F G; Maneschy, Carlos E; Chen, James; Ramalho, Teodorico C; Neto, A M J C

    2015-05-01

    Here we analyzed several physical behaviors through computational simulation of systems consisting of a zig-zag type carbon nanotube and relaxed cold atoms (Rb, Au, Si and Ar). These atoms were chosen due to their different chemical properties. The atoms individually were relaxed on the outside of the nanotube during the simulations. Each system was found under the influence of a uniform electric field parallel to the carbon nanotube and under the thermal effect of the initial temperature at the simulations. Because of the electric field, the cold atoms orbited the carbon nanotube while increasing the initial temperature allowed the variation of the radius of the orbiting atoms. We calculated the following quantities: kinetic energy, potential energy and total energy and in situ temperature, molar entropy variation and average radius of the orbit of the atoms. Our data suggest that only the action of electric field is enough to generate the attractive potential and this system could be used as a selected atoms sensor.

  6. Electron transfer and atom exchange between aqueous Fe(II) and structural Fe(III) in clays. Role in U and Hg(II) transformations

    Energy Technology Data Exchange (ETDEWEB)

    Scherer, Michelle [Univ. of Iowa, Iowa City, IA (United States)

    2016-08-31

    During this project, we investigated Fe electron transfer and atom exchange between aqueous Fe(II) and structural Fe(III) in clay minerals. We used selective chemical extractions, enriched Fe isotope tracer experiments, computational molecular modeling, and Mössbauer spectroscopy. Our findings indicate that structural Fe(III) in clay minerals is reduced by aqueous Fe(II) and that electron transfer occurs when Fe(II) is sorbed to either basal planes and edge OH-groups of clay mineral. Findings from highly enriched isotope experiments suggest that up to 30 % of the Fe atoms in the structure of some clay minerals exhanges with aqueous Fe(II). First principles calculations using a small polaron hopping approach suggest surprisingly fast electron mobility at room temperature in a nontronite clay mineral and are consistent with temperature dependent Mössbauer data Fast electron mobility suggests that electrons may be able to conduct through the mineral fast enough to enable exchange of Fe between the aqueous phase and clay mineral structure. over the time periods we observed. Our findings suggest that Fe in clay minerals is not as stable as previously thought.

  7. Atomizer

    DEFF Research Database (Denmark)

    Fixed stereo electroacoustic music, included in Robert Voisey’s (Curator) VoxNovus 60×60 Dance, 60×60 2010 International Mix and 60×60 Sanguine Mix projects. Performed internationally, including Stratford Circus, London, UK. Full performance listings and press available online....

  8. Observation of atomic carbon during photodissociation of nitrotoluenes in the vapor phase

    Science.gov (United States)

    Eilers, Hergen; Diez-y-Riega, Helena

    2014-05-01

    We perform laser-induced photodissociation fluorescence spectroscopy on mononitrotoluenes (MNTs) and dinitrotoluenes (DNTs) in the vapor phase and observe the spectrally overlapping fluorescence from nitric oxide (NO) and carbon (C). Energy-dispersive x-ray spectroscopy (EDS) and Raman spectroscopy of deposits found in the sample chamber confirm the presence of carbon. By comparing the observed fluorescence intensities with the Franck-Condon factors for NO, we are able to identify the presence or absence of fluorescence from carbon. 2-nitrotoluene and 4- nitrotoluene show carbon fluorescence for gate delays of up to 500 ns, while 2,4-dinitrotolune, 3,4-dinitrotolune, and 2,6-dinitrotolune show carbon fluorescence for gate delays of at least up to 1500 ns. The spectroscopic signal from atomic carbon in the vapor phase is observed at concentrations as low as 10 ppt. Based upon the observed S/N, detection at even lower concentrations appears feasible. Several non-nitrotoluene molecules including nitrobenzene, benzene, toluene, and CO2, are tested under identical conditions, but do not show any carbon emission. The presence of extra NO (simulation of NO pollutants) in the samples improves the S/N ratio for the detection of carbon. Energy transfer from laser-excited molecular nitrogen to NO, multiple decomposition channels in the electronic excited state of the nitrotoluene molecules, and interaction of NO with the excited-state decomposition process of the nitrotoluene molecules may all play a role.

  9. 76 FR 17751 - Hazardous Materials: Request for U.S. Competent Authority Approval of International Atomic Energy...

    Science.gov (United States)

    2011-03-30

    ... arrangement transport certificate issued in accordance with the International Atomic Energy Agency (IAEA... Authority Approval of International Atomic Energy Agency Special Arrangement CDN/ 5255/X-96 (Rev. 0... February 4, 2011, the Canadian Nuclear Safety Commission (CNSC) issued a transport license and certificate...

  10. Experimental and theoretical study of the solubility of carbon dioxide in aqueous blends of piperazine and N-methyldiethanolamine

    NARCIS (Netherlands)

    Derks, P. W. J.; Hogendoorn, J. A.; Versteeg, G. F.

    In the present study, new experimental equilibrium data are reported on the solubility of carbon dioxide into aqueous solutions of N-methyldiethanolamine (MDEA) and piperazine (PZ) over a wide range of conditions. These data not only include CO(2) solubilities and their corresponding partial

  11. Optimization of metal atomic ratio of PdxRuyNiz on carbon support for ethanol oxidation

    Science.gov (United States)

    Charoen, Kanin; Warakulwit, Chompunuch; Prapainainar, Chaiwat; Seubsai, Anusorn; Chareonpanich, Metta; Prapainainar, Paweena

    2017-11-01

    The catalytic activity of palladium (Pd) on an alloy catalyst on carbon supports with regards to ethanol oxidation was enhanced by systematically varying the atomic ratio of Pd, ruthenium (Ru), and nickel (Ni) alloy catalyst. Each atomic ratio catalyst was investigated so as to find the highest current density per mass of palladium. Functionalized carbon black (C) and reduced graphene oxide (rGO) were used as carbon supports. The PdxRuyNiz/carbon catalysts were prepared by impregnation and reduction method with sodium borohydride (NaBH4) being used as the reducing agent. Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA) were used to characterize the functionalized carbon supports, and the synthesized PdxRuyNiz/carbon catalysts were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), and inductively coupled plasma (ICP). The electrical properties of catalyst were performed by cyclic voltammetry (CV), chronoamperometry (CA), and CO-stripping to investigate the catalytic activity compared to 20%wt synthesized Pd/C. The results showed that Pd:Ru:Ni = 60:0:40 on rGO (Pd60Ni40/rGO) had the best metal atomic ratio and support for the electro-oxidation of ethanol. The maximum current density and the electrochemical surface area were 11,074 mA cm-2 mg-1Pd and 55.6 m2 g-1Pd, which were 1.7 and 2.67 times the corresponding values of synthesized Pd/C, respectively.

  12. Efficiency of Powdery Activated carbon in Ammonia-Nitrogen Removal from Aqueous Environments (Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Hatam Godini

    2017-03-01

    Full Text Available Background & Aims of the Study: Nitrogenous compounds could directly create many problems for human's health and the environment. Thus, removal of nitrogenous compounds is necessary. Among the most important problems, decreasing dissolved oxygen, toxicity for aquatics, eutrophication, converting aerobic medium into anaerobic one and corrosion could be noted. The aim of this study was determination of powdered activated carbon absorption efficiency in ammonia-nitrogen removal from aqueous environments. Materials & Methods: This study was conducted as an experimental laboratory scale. In discontinuous system, the effect of parameters including absorbent dose (0.5-1.5 gr, initial N- ammonia concentration (100-200 mg/l, pH (3-9 and contact time (2-120 min on system efficiency evaluated through Response Surface Methodology (RSM. The results were fitted into Freundlich and Langmuir absorption isotherm and then absorption by the activated carbon absorbent compared by these models and absorption were analyzed. Also, first order, semi-second order and particulate infiltration reaction kinetics were evaluated. Results: N- ammonia removal efficiency had a direct relationship with absorbent dose, pH, contact time and reverse relation with initial N-ammonia concentration. Study the isotherms and kinetics process showed that activated carbon followed Freundlich isotherm as well as semi-second order kinetics. Results from central composition design (CCD model showed that the studied system efficiency fitted to linear equation and results from model predictions had a great agreement with experimental data (R2=0. 98. Conclusion: according to appropriate removal efficiency, powdered activated carbon could be utilized as an efficient and inexpensive absorbent for ammonium absorbance. Decreasing the system efficiency by increasing pollutant concentration must be considered.

  13. 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.

  14. Reduction of Carbon Dioxide inAqueous Solutions by IonizingRadiation

    Energy Technology Data Exchange (ETDEWEB)

    Garrison, W.M.; Morrison, D.C.; Hamilton, J.G.; Benson, A.A.; Calvin, M.

    1951-03-13

    The question of the conditions under which living matter originated on the surface of the earth is still a subject limited largely to speculation. The speculation has a greater chance of approaching the truth insofar as it includes and is based upon the ever wider variety of established scientific fact. One of the purposes of the herein reported observation was to add another fact to the ever increasing information which might have any bearing upon this most interesting question. It is not our purpose in the present communication to discuss the various proposals or the arguments which have been adduced for and against them. One of the most popular current conceptions is that life originated in an organic milieu on the surface of the earth, (1,2,3,4,5). The problem to which we are addressed is the origin of that organic milieu in the absence of any life. It appeared to us that one source, if not the only source, of reduced carbon compounds in complex arrangements might be the interaction of various high energy radiations with aqueous solutions of inorganic materials, particularly carbon dioxide, and nitrogenous compounds such as ammonia and nitrogen, since it appears that these compounds were the commoner forms in which the essential elements found themselves on the primordial earth. While it has long been known that high energy radiations can cause organic decomposition and oxidation, it seemed useful to us to demonstrate that conditions could be found in which high energy radiations could induce the reduction with water of carbon dioxide and the ultimate creation of polyatomic molecules (other than simple polymerization of monomers) of carbon, oxygen, hydrogen and nitrogen.

  15. 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.

  16. Microwave absorption properties of carbon nanocoils coated with highly controlled magnetic materials by atomic layer deposition.

    Science.gov (United States)

    Wang, Guizhen; Gao, Zhe; Tang, Shiwei; Chen, Chaoqiu; Duan, Feifei; Zhao, Shichao; Lin, Shiwei; Feng, Yuhong; Zhou, Lei; Qin, Yong

    2012-12-21

    In this work, atomic layer deposition is applied to coat carbon nanocoils with magnetic Fe(3)O(4) or Ni. The coatings have a uniform and highly controlled thickness. The coated nanocoils with coaxial multilayer nanostructures exhibit remarkably improved microwave absorption properties compared to the pristine carbon nanocoils. The enhanced absorption ability arises from the efficient complementarity between complex permittivity and permeability, chiral morphology, and multilayer structure of the products. This method can be extended to exploit other composite materials benefiting from its convenient control of the impedance matching and combination of dielectric-magnetic multiple loss mechanisms for microwave absorption applications.

  17. 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(ethylcyclopentadienyl)rut......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......-up. For the compositions investigated, the catalysts with a Ru content of 29at.% exhibited highest catalytic activity....

  18. 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......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 transmission in large energy ranges. The effect is due to the spin-polarized zig-zag edge terminating each graphene flake causing a spin-splitting of the graphene pi(z) bands, and the chain states. Transmission occurs when the graphene p-states resonate with similar states in the strongly hybridized edges...

  19. An exploding N-isocyanide reagent formally composed of anthracene, dinitrogen and a carbon atom.

    Science.gov (United States)

    Joost, Maximilian; Nava, Matthew; Transue, Wesley J; Cummins, Christopher C

    2017-10-17

    Targeted as an example of a compound composed of a carbon atom together with two stable neutral leaving groups, 7-isocyano-7-azadibenzonorbornadiene, CN2A (1, A = C14H10 or anthracene) has been synthesized and spectroscopically and structurally characterized. The terminal C atom of 1 can be transferred: mesityl nitrile oxide reacts with 1 to produce carbon monoxide, likely via intermediacy of the N-isocyanate OCN2A. Reaction of 1 with [RuCl2(CO)(PCy3)2] leads to [RuCl2(CO)(1)(PCy3)2] which decomposes unselectively: in the product mixture, the carbide complex [RuCl2(C)(PCy3)2] was detected. Upon heating in the solid state or in solution, 1 decomposes to A, N2 and cyanogen (C2N2) as substantiated using molecular beam mass spectrometry, IR and NMR spectroscopy techniques.

  20. 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.

  1. 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

  2. Field-ion microscopy of quantum oscillations of linear carbon atomic chains.

    Science.gov (United States)

    Mazilova, Tatjana I; Mikhailovskij, Igor M; Ksenofontov, Vjacheslav A; Sadanov, Evgenij V

    2009-02-01

    Field ion microscopic imaging of monatomic carbon chains near the ground quantum states and the visualization of their two-dimensional wave functions were demonstrated. Quantum motions with the frequency proportional to the electric field are detected and analyzed with subangstrom lateral resolution. Electric fields above 10(10) V/m can be used for control of a transverse vibration mode of atomic chains in the terahertz spectral range.

  3. Molecular Simulation of the Diffusion of Uranyl Carbonate Species in Aqueous Solution

    Energy Technology Data Exchange (ETDEWEB)

    Kerisit, Sebastien N.; Liu, Chongxuan

    2010-09-01

    Molecular dynamics simulations of aqueous uranyl carbonate species were carried out with two different potential models to gain molecular-level insight into the hydration properties of these species and evaluate the ability of the two models to reproduce published ab initio and experimental data. The simulation results were used to estimate the self-diffusion coefficients of uranyl carbonate species that often dominate uranyl speciation in groundwater systems. The first potential model was based on a series of shell models developed by Parker and co-workers (including (DE LEEUW and PARKER, 1998; KERISIT and PARKER, 2004; PAVESE et al., 1996). The second potential model was a rigid-ion model based on the flexible SPC water model (TELEMAN et al., 1987), the uranyl model of Guilbaud and Wipff (GUILBAUD and WIPFF, 1996), and the parameters for the carbonate ion given by Greathouse and co-workers (GREATHOUSE and CYGAN, 2005; GREATHOUSE et al., 2002). Analysis of structural (mean interatomic distances and coordination numbers) and dynamical (water residence times in hydration shell and self-diffusion coefficients) properties showed that, overall, the first potential model performed best when compared to published data, although the only major discrepancy with the second model was a misrepresentation of the configuration adopted by the alkaline-earth uranyl carbonate ions. The diffusion coefficients obtained for the alkaline-earth cations and the uranyl ion were compared with three variants of the Stokes-Einstein (SE) equation and it was found that none of the three SE models were able to reproduce both the absolute values and the overall trend determined from the molecular dynamics simulations. However, as would be expected based on the SE equation, a plot of the diffusion coefficients of the uranyl carbonate complexes as a function of the inverse of the equivalent spherical radius showed a general linear dependence with the two models yielding almost identical gradients

  4. Carbon-coated ceramic membrane reactor for the production of hydrogen by aqueous-phase reforming of sorbitol.

    Science.gov (United States)

    Neira D'Angelo, M F; Ordomsky, V; Schouten, J C; van der Schaaf, J; Nijhuis, T A

    2014-07-01

    Hydrogen was produced by aqueous-phase reforming (APR) of sorbitol in a carbon-on-alumina tubular membrane reactor (4 nm pore size, 7 cm long, 3 mm internal diameter) that allows the hydrogen gas to permeate to the shell side, whereas the liquid remains in the tube side. The hydrophobic nature of the membrane serves to avoid water loss and to minimize the interaction between the ceramic support and water, thus reducing the risks of membrane degradation upon operation. The permeation of hydrogen is dominated by the diffusivity of the hydrogen in water. Thus, higher operation temperatures result in an increase of the flux of hydrogen. The differential pressure has a negative effect on the flux of hydrogen due to the presence of liquid in the larger pores. The membrane was suitable for use in APR, and yielded 2.5 times more hydrogen than a reference reactor (with no membrane). Removal of hydrogen through the membrane assists in the reaction by preventing its consumption in undesired reactions. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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

    NARCIS (Netherlands)

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

  6. 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. Copyright © 2015 Elsevier Ltd. All rights reserved.

  7. High energy density supercapacitors from lignin derived submicron activated carbon fibers in aqueous electrolytes

    Science.gov (United States)

    Hu, Sixiao; Zhang, Sanliang; Pan, Ning; Hsieh, You-Lo

    2014-12-01

    Highly porous submicron activated carbon fibers (ACFs) were robustly generated from low sulfonated alkali lignin and fabricated into supercapacitors for capacitive energy storage. The hydrophilic and high specific surface ACFs exhibited large-size nanographites and good electrical conductivity to demonstrate outstanding electrochemical performance. ACFs from KOH activation, in particular, showed very high 344 F g-1 specific capacitance at low 1.8 mg cm-2 mass loading and 10 mV s-1 scan rate in aqueous electrolytes. Even at relatively high scan rate of 50 mV s-1 and mass loading of 10 mg cm-2, a decent specific capacitance of 196 F g-1 and a remarkable areal capacitance of 0.55 F cm-2 was obtained, leading to high energy density of 8.1 Wh kg-1 based on averaged electrodes mass. Furthermore, over 96% capacitance retention rates were achieved after 5000 charge/discharge cycles. Such excellent performance demonstrated great potential of lignin derived carbons for electrical energy storage.

  8. Kinetics of adsorption of dyes from aqueous solution using activated carbon prepared from waste apricot

    Energy Technology Data Exchange (ETDEWEB)

    Onal, Yunus [Inonu University, Faculty of Engineering, Department of Chemical Engineering, 44280 Malatya (Turkey)]. E-mail: yonal@inonu.edu.tr

    2006-10-11

    Adsorbent (WA11Zn5) has been prepared from waste apricot by chemical activation with ZnCl{sub 2}. Pore properties of the activated carbon such as BET surface area, pore volume, pore size distribution, and pore diameter were characterized by N{sub 2} adsorption and DFT plus software. Adsorption of three dyes, namely, Methylene Blue (MB), Malachite Green (MG), Crystal Violet (CV), onto activated carbon in aqueous solution was studied in a batch system with respect to contact time, temperature. The kinetics of adsorption of MB, MG and CV have been discussed using six kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the Elovich equation, the intraparticle diffusion model, the Bangham equation, the modified Freundlich equation. Kinetic parameters and correlation coefficients were determined. It was shown that the second-order kinetic equation could describe the adsorption kinetics for three dyes. The dyes uptake process was found to be controlled by external mass transfer at earlier stages (before 5 min) and by intraparticle diffusion at later stages (after 5 min). Thermodynamic parameters, such as {delta}G, {delta}H and {delta}S, have been calculated by using the thermodynamic equilibrium coefficient obtained at different temperatures and concentrations. The thermodynamics of dyes-WA11Zn5 system indicates endothermic process.

  9. Facile synthesis of analogous graphene quantum dots with sp(2) hybridized carbon atom dominant structures and their photovoltaic application.

    Science.gov (United States)

    Huang, Zhengcheng; Shen, Yongtao; Li, Yu; Zheng, Wenjun; Xue, Yunjia; Qin, Chengqun; Zhang, Bo; Hao, Jingxiang; Feng, Wei

    2014-11-07

    Graphene quantum dot (GQD) is an emerging class of zero-dimensional nanocarbon material with many novel applications. It is of scientific importance to prepare GQDs with more perfect structures, that is, GQDs containing negligible oxygenous defects, for both optimizing their optical properties and helping in their photovoltaic applications. Herein, a new strategy for the facile preparation of "pristine" GQDs is reported. The method we presented is a combination of a bottom-up synthetic and a solvent-induced interface separation process, during which the target products with highly crystalline structure were selected by the organic solvent. The obtained organic soluble GQDs (O-GQDs) showed a significant difference in structure and composition compared with ordinary aqueous soluble GQDs, thus leading to a series of novel properties. Furthermore, O-GQDs were applied as electron-acceptors in a poly(3-hexylthiophene) (P3HT)-based organic photovoltaic device. The performance highlights that O-GQD has potential to be a novel electron-acceptor material due to the sp(2) hybridized carbon atom dominant structure and good solubility in organic solvents.

  10. Enhancement of oxygen reduction activity of nanoshell carbons by introducing nitrogen atoms from metal phthalocyanines

    Energy Technology Data Exchange (ETDEWEB)

    Ozaki, Jun-ichi, E-mail: jozaki@cee.gunma-u.ac.j [Department of Chemical and Environmental Engineering, Graduate School of Engineering, Gunma University, 1-5-1, Tenjin-cho, Kiryu, Gunma 376-8515 (Japan); Tanifuji, Shin-ichi; Furuichi, Atsuya; Yabutsuka, Katsutoshi [Department of Chemical and Environmental Engineering, Graduate School of Engineering, Gunma University, 1-5-1, Tenjin-cho, Kiryu, Gunma 376-8515 (Japan)

    2010-02-15

    Nanoshell carbon is a type of catalytically grown nanocarbon with a hollow, round, shell-like structure, with a diameter in the range of approximately 20-50 nm. It has been shown to possess the electrocatalytic activity for oxygen reduction reaction (ORR) and is also expected to be a non-Pt catalyst for polymer electrolyte fuel cells. This paper reports the synergetic enhancement of the ORR activity of nanoshell carbons caused by the coexistence of nitrogen atoms. The nanoshell carbons were prepared by the carbonization of furan resin in the presence of acetylacetonates (AAs) and of phthalocyanines (Pcs), which contained Fe, Co, and Ni. The Pc-derived nanoshells (MP-T series; M = Co or Fe, T = carbonization temperature) showed higher ORR activities than the AA-derived nanoshells (MA-T series; M = Co or Fe, T = carbonization temperature) when the same metal elements were employed. An XPS study revealed that nitrogen species were introduced to the surface of the nanoshells when Pcs were used as the nanoshell-forming catalysts, and that no metal species remained on the nanoshells. Principally, the ORR activity of the carbons was governed by the presence of the nanoshells and further enhancement could be achieved by the introduction of nitrogen atoms. 0.78 V of OCV and 0.21 W cm{sup -2} of the maximum power density were observed for a fuel cell whose MEA consisted of 3CoP1000 cathode and a commercial Pt/C anode, when it was operated at 80 deg. C under a pressurized condition of 0.35 MPa.

  11. 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

  12. Equilibrium magnesium isotope fractionation between aqueous Mg2+ and carbonate minerals: Insights from path integral molecular dynamics

    Science.gov (United States)

    Pinilla, Carlos; Blanchard, Marc; Balan, Etienne; Natarajan, Suresh K.; Vuilleumier, Rodolphe; Mauri, Francesco

    2015-08-01

    The theoretical determination of the isotopic fractionation between an aqueous solution and a mineral is of utmost importance in Earth sciences. While for crystals, it is well established that equilibrium isotopic fractionation factors can be calculated using a statistical thermodynamic approach based on the vibrational properties, several theoretical methods are currently used to model ions in aqueous solution. In this work, we present a systematic study to determine the reduced partition function ratio (β-factor) of aqueous Mg2+ using several levels of theory within the simulations. In particular, using an empirical force field, we compare and discuss the performance of the exact results obtained from path integral molecular dynamics (PIMD) simulations, with respect to the more traditional methods based on vibrational properties and the cluster approximation. The results show the importance of including configurational disorder for the estimation of the equilibrium isotope fractionation factor. We also show that using the vibrational frequencies computed from snapshots taken from equilibrated classical molecular dynamics represents a good approximation for the study of aqueous ions. Based on these conclusions, the β-factor of aqueous Mg2+ have been estimated from a Car-Parrinello molecular dynamics (CPMD) simulation with an ab initio force field, and combined with the β-factors of carbonate minerals (magnesite, dolomite, calcite and aragonite). Mg β-factor of Mg-bearing aragonite, calculated here for the first time, displays a lower value than the three other carbonate minerals. This is explained by a strong distortion of the cationic site leading to a decrease of the coordination number during Ca-Mg substitution. Overall, the equilibrium magnesium isotope fractionation factors between aqueous Mg2+ and carbonate minerals that derive from this methodological study support the previous theoretical results obtained from embedded cluster models.

  13. 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

  14. Ultrasound-assisted adsorption of 4-dodecylbenzene sulfonate from aqueous solutions by corn cob activated carbon.

    Science.gov (United States)

    Milenković, D D; Bojić, A Lj; Veljković, V B

    2013-05-01

    This study was aimed at removal of 4-dodecylbenzene sulfonate (DBS) ions from aqueous solutions by ultrasound-assisted adsorption onto the carbonized corn cob (AC). The main attention was focused on modeling the equilibrium and kinetics of adsorption of DBS onto the AC. The AC was prepared from ground dried corn cob by carbonization and activation by carbon dioxide at 880°C for 2h in a rotary furnace. The adsorption isotherm data were fitted by the Langmuir model in both the absence and the presence of ultrasound (US). The maximum adsorption capacities of the adsorbent for DBS, calculated from the Langmuir isotherms, were 29.41mg/g and 27.78mg/g in the presence of US and its absence, respectively. The adsorption process in the absence and the presence of US obeyed the pseudo second-order kinetics. The intraparticular diffusion model indicated that the adsorption of DBS ions on the AC was diffusion controlled as well as that US promoted intraparticular diffusion. The ΔG° values, -24.03kJ/mol, -25.78kJ/mol and -27.78kJ/mol, were negative at all operating temperatures, verifying that the adsorption of DBS ions was spontaneous and thermodynamically favorable. The positive value of ΔS°=187J/molK indicated the increased randomness at the adsorbent-adsorbate interface during the adsorption of DBS ions by the AC. Copyright © 2012 Elsevier B.V. All rights reserved.

  15. 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 as with tra......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...... as with transmission electron microscopy images, which give accurate measures for cluster widths. Despite their ideal aspect ratio, tip-broadening is concluded to be a severe problem even when imaging with carbon nanotube tips, which overestimates the cluster width by several times the nominal width of the nanotube...... tip. This broadening is attributed to a bending of the carbon nanotubes, and not to pure geometrical factors, which coincidentally results in a significant improvement for relative height measurements of tightly spaced high aspect ratio structures, as compared to what can be achieved...

  16. INDIUM AND ZINC MEDIATED ONE-ATOM CARBOCYCLE ENLARGEMENT IN WATER. (R822668)

    Science.gov (United States)

    AbstractSix-, seven-, eight-membered rings are enlarged by one carbon-atom into seven-, eight- and nine-membered ring derivatives respectively, via indium or zinc mediated reactions in aqueous medium.

  17. Microwave-induced carbon nanotubes catalytic degradation of organic pollutants in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jing; Xue, Shuang; Song, Youtao; Shen, Manli [School of Environment Science, Liaoning University, Shenyang 110036 (China); Zhang, Zhaohong, E-mail: lnuhjhx@163.com [School of Environment Science, Liaoning University, Shenyang 110036 (China); Yuan, Tianxin; Tian, Fangyuan [School of Environment Science, Liaoning University, Shenyang 110036 (China); Dionysiou, Dionysios D., E-mail: dionysios.d.dionysiou@uc.edu [Environmental Engineering and Science Program, University of Cincinnati, Cincinnati, OH 45221-0012 (United States)

    2016-06-05

    Highlights: • Microwave-induced CNTs-based catalytic degradation technology is developed. • Microwave catalytic activities of CNTs with different diameters are compared. • Organic pollutants with different structure can be degraded in MW/CNTs system. • The 10–20 nm CNTs shows the higher catalytic activity under MW irradiation. - Abstract: In this study, a new catalytic degradation technology using microwave induced carbon nanotubes (MW/CNTs) was proposed and applied in the treatment of organic pollutants in aqueous solution. The catalytic activity of three CNTs of 10–20 nm, 20–40 nm, and 40–60 nm diameters were compared. The results showed that organic pollutants such as methyl orange (MO), methyl parathion (MP), sodium dodecyl benzene sulfonate (SDBS), bisphenol A (BPA), and methylene blue (MB) in aqueous solution could be degraded effectively and rapidly in MW/CNTs system. CNTs with diameter of 10–20 nm exhibited the highest catalytic activity of the three CNTs under MW irradiation. Further, complete degradation was obtained using 10–20 nm CNTs within 7.0 min irradiation when 25 mL MO solution (25 mg/L), 1.2 g/L catalyst dose, 450 W, 2450 MHz, and pH = 6.0 were applied. The rate constants (k) for the degradation of SDBS, MB, MP, MO and BPA using 10–20 nm CNTs/MW system were 0.726, 0.679, 0.463, 0.334 and 0.168 min{sup −1}, respectively. Therefore, this technology may have potential application for the treatment of targeted organic pollutants in wastewaters.

  18. Carbon Co-Deposition During Gas Reduction of Water-Atomized Fe-Cr-Mo Powder

    Directory of Open Access Journals (Sweden)

    Ali B.

    2017-06-01

    Full Text Available The water atomization of iron powder with a composition of Fe-3Cr-0.5Mo (wt.% at 1600°C and 150 bar creates an oxide layer, which in this study was reduced using a mixture of methane (CH4 and argon (Ar gas. The lowest oxygen content was achieved with a 100 cc/min flow rate of CH4, but this also resulted in a co-deposition of carbon due to the cracking of CH4. This carbon can be used directly to create high-quality, sinter hardenable steel, thereby eliminating the need for an additional mixing step prior to sintering. An exponential relationship was found to exist between the CH4 gas flow rate and carbon content of the powder, meaning that its composition can be easily controlled to suit a variety of different applications.

  19. 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.

  20. Mechanically induced cis-to-trans isomerization of carbon-carbon double bonds using atomic force microscopy.

    Science.gov (United States)

    Radiom, Milad; Kong, Phally; Maroni, Plinio; Schäfer, Mark; Kilbinger, Andreas F M; Borkovec, Michal

    2016-11-16

    Cis-to-trans isomerization of carbon-carbon double bonds can be induced by the application of mechanical force. Using single molecule force spectroscopy by means of atomic force microscopy (AFM) we pulled polymer molecules which contained cis double bonds in the backbone. In the force versus extension profiles of these polymers, a sudden extension increase is observed which is due to the conversion of shorter cis isomers into longer trans isomers. The added length to the polymer results in relaxation in probed force. We find that the isomerization occurs at forces of 800 ± 60 pN, independent of AFM tip and solid substrate chemistries. Investigation of similar polymers which exclusively contained single bonds in the backbone showed no evidence of a similar transition.

  1. Studies on the adsorption of caesium, thallium, strontium and cobalt radionuclides on activated carbons from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Rivera-Utrilla, J.; Ferro-Garcia, M.A.; Mata-Arjona, A.; Gonzalez-Gomez, C. (Granada Univ. (Spain). Dept. of Inorganic Chemistry)

    1984-07-01

    Individual adsorption studies of Cs/sup +/, Tl/sup +/, Sr/sup 2 +/ and Co/sup 2 +/ on activated carbons from aqueous solutions are reported. The carbon samples were characterised using different techniques. The surface area and the micro-, meso- and macropore volumes of all samples have been calculated. The chemical nature of the surface of the activated carbons was also studied. Optimal conditions for the adsorption of the metal ions have been identified. The adsorption of these cations by the carbon samples was also determined in the presence of a number of different anions. The data suggest the possible use of activated carbons for the preconcentration and separation of some cations.

  2. Solid sampling high-resolution continuum source graphite furnace atomic absorption spectrometry for gold determination in geological samples after preconcentration onto carbon nanotubes

    Science.gov (United States)

    Dobrowolski, Ryszard; Mróz, Agnieszka; Dąbrowska, Marzena; Olszański, Piotr

    2017-06-01

    A novelty method for the determination of gold in geological samples by solid sampling high-resolution continuum source graphite furnace atomic absorption spectrometry (SS HR CS GF AAS) after solid-phase extraction onto modified carbon nanotubes (CNT) was described. The methodology developed is based on solid phase extraction of Au(III) ions from digested samples to eliminate strong interference caused by iron compounds and problems related to inhomogeneities of the samples. The use of aqueous or solid standard for calibration was studied and the slope of calibration curve was the same for both of these modes. This statement indicates the possibility to perform the calibration of the method using aqueous standard solutions. Under optimum conditions the absolute detection limit for gold was equal to 2.24 · 10- 6 μg g- 1 while the adsorption capacity of modified carbon nanotubes was 264 mg g- 1. The proposed procedure was validated by the application of certified reference materials (CRMs) with different content of gold and different matrix, the results were in good agreement with certified values. The method was successfully applied for separation and determination of gold ions in complex geological samples, with precision generally better than 8%.

  3. Electrodeposition of tantalum on carbon black in non-aqueous solution and its electrocatalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Jo, Ara; Lee, Youngmi, E-mail: youngmilee@ewha.ac.kr; Lee, Chongmok, E-mail: cmlee@ewha.ac.kr

    2016-08-24

    In this work, we synthesized tantalum (Ta) nanoclusters on carbon black (Ta/CB) via simple electrodeposition in non-aqueous solvent, acetonitrile (ACN) at ambient temperature. Transmission electron microscopy (TEM) images showed that the electrodeposited Ta nanoclusters consisted of tiny Ta nanoparticles. X-ray photoelectron spectroscopy (XPS) result represented that the outermost Ta formed the native oxide on Ta/CB due to its ambient exposure to air. Electrochemical catalytic properties of prepared Ta/CB on glassy carbon electrode (Ta/CB/GC) were investigated toward reductions of oxygen and hydrogen peroxide, and oxidations of ascorbic acid and dopamine. For oxygen reduction reaction (ORR) in acid, Ta/CB/GC represented a decent electrocatalytic performance which was better or comparable to bare Pt. The operational stability in acidic condition was maintained up to 500 repetitive potential cycles presumably due to the protective native Ta oxide layer. Ta/CB/GC also showed high amperometric sensitivity (4.5 (±0.1{sub 6}) mA mM{sup −1} cm{sup −2}, n = 5) for reduction of hydrogen peroxide in 0.1 M phosphate buffer solution (PBS, pH 7.4). In addition, Ta/CB/GC was demonstrated for the possibility of simultaneous detection of ascorbic acid and dopamine using differential pulse voltammetry (DPV). - Highlights: • We electrodeposited Ta nanoclusters (Ta/CB/GC) in acetonitrile at room temperature. • The Ta/CB/GC showed better or comparable performance to bare Pt for ORR. • The Ta/CB/GC showed high sensitivity for reduction of hydrogen peroxide at pH 7.4. • The Ta/CB/GC showed possible simultaneous detection of ascorbic acid and dopamine. • We extended the applicability of Ta electrode material for various electrocatalytic reactions.

  4. Chlorinated phenol removal from aqueous media by tea (Camellia sinensis) leaf waste tailored activated carbon

    Science.gov (United States)

    Joseph, C. G.; Anisuzzaman, S. M.; Daud, W. M. A. W.; Krishnaiah, D.; Ng, K. A.

    2017-06-01

    In this study, activated carbons (ACs) wereprepared from tea leaves by using a two-stage self-generated atmosphere method. The process was done by semi-carbonizing the precursor at 300 °C for 1 h, followed by the impregnation of the resulting char at 85 °C for 4 h and finally activation at 500 °C for 2 h. The semi-carbonised samples were impregnated with different ratios of zinc chloride (ZnCl2) and their physicochemical effect was studied. The prepared ACs underwent several aspects of both, chemical and physical characterizations, such as the percentage of yield, moisture content, ash content, pH, porosity, adsorption capacity of 2,4-dichlorophenol (2,4-DCP), surface area, porosity, morphology and surface chemistry studies. It was found that sample AC2, with an impregnation ratio of 2:1 was the best AC produced in this study. The maximum Brunauer, Emmett and Teller surface area of AC2 was found to be 695 m2/g. Langmuir, Freundlich and Temkin isotherm models were used to examine the experimental isotherms while the kinetic data was analyzed using the pseudo-first-order, pseudo-second-order and intraparticle diffusion kinetic models. The 2,4-DCP adsorption isotherm results complied well to the Langmuir isotherm for the equilibrium data while the adsorption kinetic data fitted well to the pseudo-second order model, indicating that chemisorption by valency forces via the sharing (covalent bond) or exchanging of electrons between the AC and the 2,4-DCP molecules were mainly responsible for the adsorption process. From these findings, it is concluded that tea leaves can be used as a low cost precursor for the removal of 2,4-DCP in aqueous medium.

  5. Determining Nuclear Fingerprints: Glove Boxes, Radiation Protection, and the International Atomic Energy Agency.

    Science.gov (United States)

    Rentetzi, Maria

    2017-06-01

    In a nuclear laboratory, a glove box is a windowed, sealed container equipped with two flexible gloves that allow the user to manipulate nuclear materials from the outside in an ostensibly safe environment. As a routine laboratory device, it invites neglect from historians and storytellers of science. Yet, since especially the Gulf War, glove boxes have put the interdependence of science, diplomacy, and politics into clear relief. Standing at the intersection of history of science and international history, technological materials and devices such as the glove box can provide penetrating insight into the role of international diplomatic organizations to the global circulation and control of scientific knowledge. The focus here is on the International Atomic Energy Agency. Copyright © 2017 The Author. Published by Elsevier Ltd.. All rights reserved.

  6. 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%.

  7. 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.

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

    Directory of Open Access Journals (Sweden)

    Tramontina Jucelânia

    2001-01-01

    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.

  9. Electropolymerization of phenol on a vitreous carbon electrode in alkaline aqueous solution at different temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Belhadj Tahar, Noureddine [Departement de Chimie, Faculte des Sciences de Monastir, Universite de Monastir, Route de Kairouan, 5000 Monastir (Tunisia); Savall, Andre, E-mail: savall@chimie.ups-tlse.f [Laboratoire de Genie Chimique, CNRS, Universite Paul Sabatier, 118 Route de Narbonne, 31062 Toulouse (France)

    2009-12-30

    Electrochemical oxidation of phenol in basic aqueous solution has been studied on a vitreous carbon electrode at different temperatures in the range of 25-85 deg. C by cyclic voltammetry and chronoamperometry techniques. The electrochemical oxidation of phenol led to a complete deactivation of the electrode, whatever the temperature used, as a result of the deposition of an adhesive and insulating polymeric film. The electrochemical activity of the electrode was progressively restored by repeated potential scans in the range of water stability only when conducted at high temperatures; electrode reactivation was explained by an increase in the polymeric film permeability for both electrons (electron tunneling) and phenol molecules (diffusion). Chronoamperometric measurements carried out in the potential region of water stability have shown that electrode passivation was reduced or prevented at high temperatures. For chronoamperometry performed at the onset of oxygen evolution, the electrode remained active even at low temperatures because the discharge of water involved the production of hydroxyl radicals that destructively oxidized the polymeric film. The effect of temperature on electrode reactivation was determined by the measurement of current at an electrolysis time of 300 s; an increase of the temperature from 25 to 85 deg. C amplified the current from 0.212 to 5.373 mA.

  10. Adsorption equilibrium and kinetics of polyvinyl alcohol from aqueous solution on powdered activated carbon.

    Science.gov (United States)

    Behera, Shishir Kumar; Kim, Jung-Hoon; Guo, Xuejun; Park, Hung-Suck

    2008-05-30

    In this study, powdered activated carbon (PAC) was used to remove polyvinyl alcohol (PVA) from the aqueous PVA solution. The adsorption kinetics has been studied pertaining to various initial PVA concentration and PAC dosage. The rates of adsorption were found to conform to the second-order kinetics with good correlation. Boyd plot confirmed that external mass transfer was the rate-limiting step in the sorption process. The adsorption isotherm obtained resembled with H-type of isotherm, which indicated a high affinity of the solute for the sorption sites. The Freundlich model appeared to fit the isotherm data better than the Langmuir model. The thermodynamic parameters such as Delta H degrees , Delta S degrees and Delta G degrees were evaluated from the slope and intercept of linear plot of log Kc against (1/T) x 1000. The change in entropy (DeltaS degrees ) and heat of adsorption (Delta H degrees ) of PAC was estimated as 1.45 kJ mol(-1)K(-1) and 365 kJ mol(-1), respectively. The free energy of the adsorption at all temperatures was negative indicating a spontaneous process. The maximum PVA removal of 92% was obtained at a pH of 6.3 and contact time of 30 min for an adsorbent dose of 5 g/L.

  11. Adsorption of quinolone, tetracycline, and penicillin antibiotics from aqueous solution using activated carbons: Review.

    Science.gov (United States)

    Ahmed, Muthanna J

    2017-03-01

    Antibiotics, an important type of pharmaceutical pollutant, have attracted many researchers to the study of their removal from aqueous solutions. Activated carbon (AC) has been widely used as highly effective adsorbent for antibiotics because of its large specific surface area, high porosity, and favorable pore size distribution. In this article, the adsorption performance of AC towards three major types of antibiotics such as tetracyclines, quinolones, and penicillins were reviewed. According to collected data, maximum adsorption capacities of 1340.8, 638.6, and 570.4mg/g were reported for tetracyclines, quinolones, and penicillins, respectively. The values of 1/n for Freundlich isotherm were less than unity, suggesting that the adsorption was nonlinear and favorable. Adsorption kinetics followed closely the pseudo-second-order model and analysis using the Weber-Morris model revealed that the intra-particle diffusion was not the only rate controlling step. AC adsorption demonstrated superior performance for all selected drugs, thus being efficient technology for treatment of these pollutants. Copyright © 2017 Elsevier B.V. All rights reserved.

  12. Adsorptive removal of aniline by granular activated carbon from aqueous solutions with catechol and resorcinol.

    Science.gov (United States)

    Suresh, S; Srivastava, V C; Mishrab, I M

    2012-01-01

    In the present paper, the removal of aniline by adsorption process onto granular activated carbon (GAC) is reported from aqueous solutions containing catechol and resorcinol separately. The Taguchi experimental design was applied to study the effect of such parameters as the initial component concentrations (C(0,i)) of two solutes (aniline and catechol or aniline and resorcinol) in the solution, temperature (T), adsorbent dosage (m) and contact time (t). The L27 orthogonal array consisting of five parameters each with three levels was used to determine the total amount of solutes adsorbed on GAC (q(tot), mmol/g) and the signal-to-noise ratio. The analysis of variance (ANOVA) was used to determine the optimum conditions. Under these conditions, the ANOVA shows that m is the most important parameter in the adsorption process. The most favourable levels of process parameters were T = 303 K, m = 10 g/l and t = 660 min for both the systems, qtot values in the confirmation experiments carried out at optimum conditions were 0.73 and 0.95 mmol/g for aniline-catechol and aniline-resorcinol systems, respectively.

  13. Adsorptive removal of nickel from aqueous solutions by activated carbons from doum seed (Hyphaenethebaica coat

    Directory of Open Access Journals (Sweden)

    Manal El-Sadaawy

    2014-06-01

    Full Text Available The present study investigates the possibility of using low cost agriculture waste as doum-palm seed coat for the removal of nickel ions from aqueous solutions. Two activated carbons had been prepared from raw doum-palm seed coat (DACI and DACII; as well, the raw material was used as an adsorbent (RD. Batch adsorption experiments were performed as a function of pH of solution, initial nickel ions concentration, dose of adsorbent and contact time. Adsorption data were modeled using Langmuir, Freundlich, Temkin and D–R Models. Different error analysis conforms that the isotherm data followed Freundlich models for all adsorbents. Adsorption kinetic data were tested using pseudo-first order, pseudo-second order and Elovich model. Adsorption mechanism was investigated using the intra-particle diffusion model. Diffusion coefficients were calculated using the film and intraparticle diffusion models. Kinetic studies showed that the adsorption of Ni2+ ions onto RD, DACI and DACII followed pseudo-second order kinetic model, and indicates that the intra-particle diffusion controls the rate of adsorption but it is not the rate limiting step.

  14. Characteristics of cesium ion sorption from aqueous solution on bentonite- and carbon nanotube-based composites.

    Science.gov (United States)

    Yang, Shubin; Han, Cho; Wang, Xiangke; Nagatsu, Masaaki

    2014-06-15

    The technology development of Cs(+) capture from aqueous solution is crucial for the disposal of nuclear waste and still remains a significant challenge. Previous researches have been proven that ion exchanges with the cations and hydroxyl exchange are the main sorption mechanisms for Cs(+). Therefore, how important are the cation exchange and the hydroxyl exchange mechanisms to Cs(+) sorption? And whether can we improve the sorption capacity of the material by increasing the amount of hydroxyl groups? With these in mind, we herein designed the chitosan-grafted carbon nanotubes (CS-g-CNTs) and the chitosan-grafted bentonite (CS-g-bentonite) by plasma-induced grafting method. The interactions of Cs(+) with CNTs, bentonite, CS-g-CNTs and CS-g-bentonite composites were investigated. The sorption of Cs(+) is mainly dominated by strong cation exchange in monovalent Group I and divalent Group II. And the cation-exchange mechanism is much more effective than the hydroxyl group exchange. The effect of hydroxyl groups is dependent on the property of the matrix. We cannot improve the Cs adsorption capacity of material for Cs(+) only by increasing the amount of hydroxyl groups in any case. The spatial structure and the cation-exchange capacity of the material are important factors for choosing the sorbent for Cs(+) removal from radioactive waste water. Copyright © 2014 Elsevier B.V. All rights reserved.

  15. Chromium (Ⅵ) removal from aqueous solutions through powdered activated carbon countercurrent two-stage adsorption.

    Science.gov (United States)

    Wang, Wenqiang

    2018-01-01

    To exploit the adsorption capacity of commercial powdered activated carbon (PAC) and to improve the efficiency of Cr(VI) removal from aqueous solutions, the adsorption of Cr(VI) by commercial PAC and the countercurrent two-stage adsorption (CTA) process was investigated. Different adsorption kinetics models and isotherms were compared, and the pseudo-second-order model and the Langmuir and Freundlich models fit the experimental data well. The Cr(VI) removal efficiency was >80% and was improved by 37% through the CTA process compared with the conventional single-stage adsorption process when the initial Cr(VI) concentration was 50 mg/L with a PAC dose of 1.250 g/L and a pH of 3. A calculation method for calculating the effluent Cr(VI) concentration and the PAC dose was developed for the CTA process, and the validity of the method was confirmed by a deviation of <5%. Copyright © 2017. Published by Elsevier Ltd.

  16. Adsorption of triazine herbicides from aqueous solution by functionalized multiwall carbon nanotubes grown on silicon substrate

    Science.gov (United States)

    D’Archivio, Angelo Antonio; Maggi, Maria Anna; Odoardi, Antonella; Santucci, Sandro; Passacantando, Maurizio

    2018-02-01

    Multi-walled carbon nanotubes (MWCNTs), because of their small size and large available surface area, are potentially efficient sorbents for the extraction of water solutes. Dispersion of MWCNTs in aqueous medium is suitable to adsorb organic contaminants from small sample volumes, but, the recovery of the suspended sorbent for successive re-use represents a critical step, which makes this method inapplicable in large-scale water-treatment technologies. To overcome this problem, we proposed here MWCNTs grown on silicon supports and investigated on a small-volume scale their adsorption properties towards triazine herbicides dissolved in water. The adsorption efficiency of the supported MWCNTs has been tested on seven triazine herbicides, which are emerging water contaminants in Europe and USA, because of their massive use, persistence in soils and potential risks for the aquatic organisms and human health. The investigated compounds, in spite of their common molecular skeleton, cover a relatively large property range in terms of both solubility in water and hydrophilicity/hydrophobicity. The functionalisation of MWCNTs carried out by acidic oxidation, apart from increasing wettability of the material, results in a better adsorption performance. Increasing of functionalisation time between 17 and 60 h progressively increases the extraction of all seven pesticides and produces a moderate increment of selectivity.

  17. 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.

  18. 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.

  19. 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.

  20. Advances in preparation of modified activated carbon and its applications in the removal of chromium (VI) from aqueous solutions

    Science.gov (United States)

    Deng, Z. L.; Liang, M. N.; Li, H. H.; Zhu, Z. J.

    2016-08-01

    The wastewater in which Cr(VI) is not fully treated has drawn environment researchers’ attention increasingly, due to its environmental pollution and harms to human health. Thus a high efficiency of modified activated carbon (MAC) to remove Cr(VI) has become one of the hot topics among environmental material research. This paper introduces the modification methods from the physical structure features and chemical properties of the activated carbon (AC) surface. At the same time, it briefly analyses the chemical characteristics of Cr(VI) in aqueous solutions, and on the basis of the aforementioned introduces the modification methods of the surface chemical characteristics of AC, such as: oxidation modification, reduction modification, loaded metal modification, and microwave modification. Combining studies on removing Cr(VI) from aqueous solutions by MAC in recent years, this paper anticipates the new trends of preparing MAC and the points in absorption research, offering some suggestions for future studies.

  1. 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.

  2. Determination of barium and strontium by atomic absorption in aqueous solutions with (Sr)/(Ba) ratios ranging from 0. 04 to 15,000

    Energy Technology Data Exchange (ETDEWEB)

    Galinier, C.; Bouhlel, S.; Reynier, B.

    1986-11-01

    The systematic use of atomic absorption allowed the determination of Ba and Sr in aqueous solutions with (Sr)/(Ba) ratios ranging from 0.04 to 15,000. In this study, we define the limits over which the interaction between the matrix and the ion to determine becomes important. For concentration ratios (Sr)/(Ba) lower than 50, the addition of lg of KCl per liter reduces the effect of the matrix to a reasonable value. For an (Sr)/(Ba) ratio above 50, adding an alcaline salt is not sufficient to decrease the interactions. In this case, we propose a diagram to correct the determination of baryum.

  3. Alumino-silicate catalyst and use for aromatization of hydrocarbons comprising 5 to 12 carbon atoms

    Energy Technology Data Exchange (ETDEWEB)

    Alario, F.; Deves, J.M.

    1993-05-21

    The invention describes a composite catalyst which contains: a MFI structure zeolite in the form hydrogen, containing in its structure Silicon, Aluminium and / or Gallium at least; a matrix; platinum metals at least and additive metal chosen among Stain, Germanium, Indium, Copper, Iron, Molybdenum, Gallium, Thallium, Gold, Silver, Ruthenium, Chrome, Tungsten and Lead at least; an halogen chosen among Fluorine, Chlorine, Bromine and Iodine at least; possibly, doping element chosen among Gallium and Zinc and possibly alkaline or alkaline-earth metal in the matrix preferentially. The invention describes also the use of this catalyst for aromatization reactions of hydrocarbons containing 5 to 12 carbon atoms per molecule.

  4. An aromatization process for hydrocarbons containing from 2 to 4 carbon atoms per molecule

    Energy Technology Data Exchange (ETDEWEB)

    Alario, F.; Renard, P.

    1993-12-17

    The aromatization process consists in introducing a fraction composed of 2 to 4 carbon atoms per molecule compounds in a reaction zone which comprises: a first reaction space composed of at least one elementary catalytic zone of the fixed bed type (in which the fraction circulates); and a second reaction space with at least an elementary catalytic zone where the fraction circulates. This space is designed in such a way that the granular catalyst is progressively drawn-off from the last elementary zone, regenerated and subsequently re-introduced in the first elementary zone. 4 tabs.

  5. An aromatization process for hydrocarbons containing from 5 to 12 carbon atoms per molecule

    Energy Technology Data Exchange (ETDEWEB)

    Alario, F.; Renard, P.; Berthelin, M.; Thery, M.

    1993-12-17

    The aromatization process consists in introducing a fraction composed of 5 to 12 carbon atoms per molecule compounds in a reaction zone which comprises: a first reaction space composed of at least one elementary catalytic zone of the fixed bed type (in which the fraction circulates); and a second reaction space with at least an elementary catalytic zone where the fraction circulates. This space is designed in such a way that the granular catalyst is progressively drawn-off from the last elementary zone, regenerated and subsequently re-introduced in the first elementary zone. 2 tabs.

  6. MFI structure catalyst and utilization for aromatization hydrocarbons comprising 5 to 12 carbon atoms

    Energy Technology Data Exchange (ETDEWEB)

    Alario, F.; Deves, J.M.

    1993-05-21

    The invention describes a composite catalyst which contains: a MFI structure zeolite containing, at least, an element chosen among alkaline or alkaline-earth metals, with a structure made of Silicon, Aluminium and / or Gallium; a matrix; platinum metals and additive metal chosen among Stain, Germanium, Indium, Copper, Iron, Molybdenum, Gallium, Thallium, Gold, Silver, Ruthenium, Chrome, Tungsten and Lead at least; an halogen chosen among Fluorine, Chlorine, Bromine and Iodine at least; Gallium and Zinc possibly; alkaline or alkaline-earth metal in the matrix preferentially. The invention describes also the use of this catalyst for aromatization reactions of hydrocarbons containing 5 to 12 carbon atoms per molecule.

  7. Building a multi-walled carbon nanotube-based mass sensor with the atomic force microscope

    DEFF Research Database (Denmark)

    Mateiu, Ramona Valentina; Kuhle, A.; Marie, Rodolphe Charly Willy

    2005-01-01

    are used. The gold substrate is first covered with hydrophobic thiol molecules: octadecanthiol. The octadecanthiol molecules are then selectively removed from small areas by nanoshaving the gold substrate with the tip of an atomic force microscope (AFM) operating in contact mode. Hydrophilic thiols (2......We report an approach for building a mass sensor based on multi-walled carbon nanotubes (MWCNT). We propose a method with a great potential for the positioning of MWCNTs based on self-assembly onto patterned hydrophilic areas. For the experiments ultra flat mica substrates covered with gold...

  8. Formation of cerussite and hydrocerussite during adsorption of lead from aqueous solution on oxidized carbons by cold oxygen plasma

    Energy Technology Data Exchange (ETDEWEB)

    De Velasco Maldonado, Paola S. [Instituto Tecnologico de Aguascalientes, Av. Adolfo López Mateos No. 1801 Ote. C.P, Aguascalientes, Ags, 20256 (Mexico); Hernández-Montoya, Virginia, E-mail: virginia.hernandez@yahoo.com.mx [Instituto Tecnologico de Aguascalientes, Av. Adolfo López Mateos No. 1801 Ote. C.P, Aguascalientes, Ags, 20256 (Mexico); Concheso, A.; Montes-Morán, Miguel A. [Instituto Nacional del Carbon, INCAR-CSIC, Apartado 73, E-33080, Oviedo (Spain)

    2016-11-15

    Highlights: • The formation of cerussite and hydrocerussite was observed on the carbon surface. • Occurrence of CaCO{sub 3} on the carbons surface plays a crucial role in the formation. • The carbons were prepared by carbonization and oxidation with cold oxygen plasma. • Oxidation with cold oxygen plasma increases the formation of these compounds. - Abstract: A new procedure of elimination of Pb{sup 2+} from aqueous solution using carbon adsorbents, in which high amounts of cerussite and hydrocerussite are deposited on the carbon surfaces, is reported. The procedure includes the preparation of carbons from selected lignocellulosic wastes (pecan nut shells and peach stones) by single carbonization and further oxidation with cold oxygen plasma. The materials prior and after the oxidation treatment were characterized using elemental analysis, FT-IR spectroscopy, SEM/EDX analysis, adsorption of N{sub 2} at −196 °C and X-ray photoelectron spectroscopy. The adsorption of Pb{sup 2+} was carried out in batch systems under constant agitation. The formation of cerussite and hydrocerussite on the spent carbon surfaces was confirmed by XRD, SEM/EDX and FT-IR. A Pb{sup 2+} removal mechanism is proposed in which a co-precipitation of lead nitrate and calcium carbonate would render the formation of the lead carbonates. In such mechanism, the occurrence of CaCO{sub 3} on the surface of the adsorbents plays a crucial role. The presence of calcium carbonate on the precursors is understood on the basis of the thermal evolution of calcium oxalate originally present in the biomass. The oxygen plasma treatment helps to expose the calcium carbonate nanocrystals thus improving dramatically the removal capacity of Pb{sup 2+}. Accordingly, retention capacities as high as 63 mg of Pb{sup 2+} per gram of adsorbent have been attained.

  9. Magnesium bicarbonate and carbonate interactions in aqueous solutions: An infrared spectroscopic and quantum chemical study

    Science.gov (United States)

    Stefánsson, Andri; Lemke, Kono H.; Bénézeth, Pascale; Schott, Jacques

    2017-02-01

    The interaction of magnesium with bicarbonate and carbonate ions in aqueous solutions was studied using infrared spectroscopy and quantum chemical calculations. Using the infrared vibrational bands for HCO3- and CO32- at 1200-1450 cm-1 (δC-OH, vS and v3) together with their molar absorptivity (ε), the concentrations of the HCO3- and CO32- ions and the corresponding Mg ion pairs have been determined. In the absence of Mg2+, measured spectra were accurately reproduced assuming that only HCO3- and CO32- were present in solution. Upon addition of Mg2+ at fixed pH, infrared spectra were observed to shift indicating presence of the MgHCO3+ and MgCO3 (aq) ion pairs. From measurements, the second ionization constant of carbonic acid and the MgHCO3+ and MgCO3 (aq) ion pair formation constants have been obtained, these being logK2 = -10.34 ± 0.04, logKMgHCO3+ = 1.12 ± 0.11 and logKMgCO3 = 2.98 ± 0.06, respectively. To support our experimental infrared measurements and to gain further insight into the molecular nature of the ion pair formation, density functional theory (DFT) calculations with VPT2 anharmonic correction were conducted. The most stable geometries predicted for the MgHCO3+ and MgCO3 (aq) ion pairs were a bi-dentate [MgHCO3]+(H2O)n and a monodentate [MgHCO3]+(OH)(H2O)n complexes, respectively. The predicted frequencies for HCO3-, CO32- and MgHCO3+ were found to shift toward those experimentally measured with an increasing H2O solvation number where possible band shifts were predicted for MgCO3 (aq) relative to CO32-, this being dependent on the exact structure and hydration of the bulk MgCO3 (aq) ion pair. Experimentally, the ion pair formations were found to have insignificant effects on the δC-OH, vS and v3 vibrational frequencies. The speciation of dissolved inorganic carbon may be significantly influenced by ion pair formation, particularly in alkaline solutions where they may be the predominant species.

  10. Adsorption of Reactive Blue 171 from Aqueous Solution using Low Cost Activated Carbon Prepared from Agricultural Solid Waste: Albizia amara

    Directory of Open Access Journals (Sweden)

    K. Anitha

    2015-07-01

    Full Text Available The adsorption of Reactive Blue 171 (Reactive Dye from aqueous solution using activated carbon prepared from Albizia amara pod shell waste as an adsorbent have been carried out. The experimental adsorption data fitted reasonably well to Langmuir and Freundlich adsorption isotherms. Kinetic parameters as a function of Initial dye concentration have been calculated and the kinetic data were substituted in Pseudo First Order, Elovich and Pseudo Second order equations. A probable explanation is offered to account for the results of kinetic study. The thermodynamic parameter enthalpy change (∆H suggests the exothermic nature of absorption of Reactive Blue 171 onto activated Albizia amara pod shell waste carbon.

  11. 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.

  12. 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.

  13. Increasing the Strength of Single Filaments and Yarns of a Paraaramid Fiber by Their Processing with an Aqueous Suspension of Carbon Nanoparticles

    Science.gov (United States)

    Shebanov, S. M.; Novikov, I. K.; Gumargalieva, K. Z.; Pavlikov, A. V.

    2017-05-01

    The paper presents the results of increasing the strength and modulus of single filaments and yarns of a paraaramid fiber by their processing with an aqueous suspension of carbon nanotubes in the production process

  14. Raman spectroscopy as a tool to investigate the structure and electronic properties of carbon-atom wires

    Directory of Open Access Journals (Sweden)

    Alberto Milani

    2015-02-01

    Full Text Available Graphene, nanotubes and other carbon nanostructures have shown potential as candidates for advanced technological applications due to the different coordination of carbon atoms and to the possibility of π-conjugation. In this context, atomic-scale wires comprised of sp-hybridized carbon atoms represent ideal 1D systems to potentially downscale devices to the atomic level. Carbon-atom wires (CAWs can be arranged in two possible structures: a sequence of double bonds (cumulenes, resulting in a 1D metal, or an alternating sequence of single–triple bonds (polyynes, expected to show semiconducting properties. The electronic and optical properties of CAWs can be finely tuned by controlling the wire length (i.e., the number of carbon atoms and the type of termination (e.g., atom, molecular group or nanostructure. Although linear, sp-hybridized carbon systems are still considered elusive and unstable materials, a number of nanostructures consisting of sp-carbon wires have been produced and characterized to date. In this short review, we present the main CAW synthesis techniques and stabilization strategies and we discuss the current status of the understanding of their structural, electronic and vibrational properties with particular attention to how these properties are related to one another. We focus on the use of vibrational spectroscopy to provide information on the structural and electronic properties of the system (e.g., determination of wire length. Moreover, by employing Raman spectroscopy and surface enhanced Raman scattering in combination with the support of first principles calculations, we show that a detailed understanding of the charge transfer between CAWs and metal nanoparticles may open the possibility to tune the electronic structure from alternating to equalized bonds.

  15. Ultrastable combined atomic force and total internal reflection fluorescence microscope [corrected].

    Science.gov (United States)

    Gumpp, H; Stahl, S W; Strackharn, M; Puchner, E M; Gaub, H E

    2009-06-01

    Combining atomic force microscope (AFM) with other microscopy techniques has expanded the range of potential applications for single molecule investigations dramatically. Particularly hybrid instruments with total internal reflection fluorescence (TIRF) excitation have opened new routes in life sciences. Here we present a novel design for such a hybrid microscope, which overcomes the limitations of conventional combinations caused by their limited mechanical stability. A thorough analysis of the noise spectra and a comparison of the different designs and the different operation modes are given. With this instrument we demonstrate single molecule manipulation by AFM and simultaneous TIRF imaging.

  16. Sorption of aqueous Zn[II] and Cd[II] by multiwall carbon nanotubes: the relative roles of oxygen-containing functional groups and graphenic carbon.

    Science.gov (United States)

    Cho, Hyun-Hee; Wepasnick, Kevin; Smith, Billy A; Bangash, Fazlullah K; Fairbrother, D Howard; Ball, William P

    2010-01-19

    Exposure of multiwalled carbon nanotubes (MWCNTs) to oxidizing acids and other oxidants introduces oxygen-containing functional groups such as hydroxyl, carboxyl, and carbonyl groups onto the surface. This research evaluated how changes in oxygen concentration and distribution of oxygen-containing functional groups influenced the sorption of aqueous zinc and cadmium on MWCNTs. Sorption results with natural char, activated carbon, and a suite of MWCNTs (of varying surface oxygen content) were obtained. Results confirmed that surface oxygen enhances the sorption of both Zn[II] and Cd[II] from aqueous solution. Although Zn[II] sorbed more strongly than Cd[II] for all materials studied, surface oxidation had more effect on the sorption of Cd[II] than of Zn[II]. Additional sorption experiments with Zn[II] and 16 MWCNTs of varying surface oxidation level and functional group distribution revealed the relative contributions of different types of surface sites to sorption. Sorption isotherms were fit using a two-site Langmuir adsorption model that incorporated the independent characterization of functional group distribution. Results showed that carboxyl-carbon sites were over 20 times more energetic for zinc sorption than unoxidized carbon (graphenic-carbon) sites, though both site types are important contributors to sorption.

  17. Extracting alcohols from aqueous solutions. [USDOE patent application

    Science.gov (United States)

    Compere, A.L.; Googin, J.M.; Griffith, W.L.

    1981-12-02

    The objective is to provide an efficient process for extracting alcohols in aqueous solutions into hydrocarbon fuel mixtures, such as gasoline, diesel fuel and fuel oil. This is done by contacting an aqueous fermentation liquor with a hydrocarbon or hydrocarbon mixture containing carbon compounds having 5-18 carbon atoms, which may include gasoline, diesel fuel or fuel oil. The hydrocarbon-aqueous alcohol solution is then mixed with one or more of a group of polyoxyalkylene polymers to extract the alcohol into the hydrocarbon fuel-polyoxyalkylene polymer mixture.

  18. Bismuth as a general internal standard for lead in atomic absorption spectrometry.

    Science.gov (United States)

    Bechlin, Marcos A; Fortunato, Felipe M; Ferreira, Edilene C; Gomes Neto, José A; Nóbrega, Joaquim A; Donati, George L; Jones, Bradley T

    2014-06-11

    Bismuth was evaluated as internal standard for Pb determination by line source flame atomic absorption spectrometry (LS FAAS), high-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS) and line source graphite furnace atomic absorption spectrometry (LS GFAAS). Analysis of samples containing different matrices indicated close relationship between Pb and Bi absorbances. Correlation coefficients of calibration curves built up by plotting A(Pb)/A(Bi)versus Pb concentration were higher than 0.9953 (FAAS) and higher than 0.9993 (GFAAS). Recoveries of Pb improved from 52-118% (without IS) to 97-109% (IS, LS FAAS); 74-231% (without IS) to 96-109% (IS, HR-CS FAAS); and 36-125% (without IS) to 96-110% (IS, LS GFAAS). The relative standard deviations (n=12) were reduced from 0.6-9.2% (without IS) to 0.3-4.3% (IS, LS FAAS); 0.7-7.7% (without IS) to 0.1-4.0% (IS, HR-CS FAAS); and 2.1-13% (without IS) to 0.4-5.9% (IS, LS GFAAS). Copyright © 2014 Elsevier B.V. All rights reserved.

  19. 2nd International School of Physics of Exotic Atoms "Ettore Majorana"

    CERN Document Server

    Duclos, J; Fiorentini, Giovanni; Torelli, Gabriele; Exotic atoms : fundamental interactions and structure of matter

    1980-01-01

    The second course of the International School on the Physics of Exotic Atoms took place at the "Ettore Majorana" Center for Scien­ tific Culture, Erice, Sicily, during the period from March 25 to April 5, 1979. It was attended by 40 participants from 23 insti­ tutes in 8 countries. The purpose of the course was to review the various aspects of the physics of exotic atoms, with particular emphasis on the re­ sults obtained in the last two years, i.e., after the first course of the School (Erice, April 24-30, 1977). The course dealt with two main topics, A) Exotic atoms and fundamental interactions and B) Applications to the study of the structure of matter. One of the aims of the course was to offer an opportunity for the exchange of experiences between scientists working in the two fields. In view of this, the lectures in the morning discussed the more general arguments in a common session, whereas the more specialized topics were treated in the afternoon, in two parallel sections. Section A was or...

  20. Hexavalent chromium adsorption from aqueous solution using carbon nano-onions (CNOs).

    Science.gov (United States)

    Sakulthaew, Chainarong; Chokejaroenrat, Chanat; Poapolathep, Amnart; Satapanajaru, Tunlawit; Poapolathep, Saranya

    2017-10-01

    The capacity of carbon nano-onions (CNOs) to remove hexavalent chromium (Cr(VI)) from aqueous solution was investigated. Batch experiments were performed to quantify the effects of the dosage rate, pH, counter ions, and temperature. The adsorption of Cr(VI) onto CNOs was best described by a pseudo-second order rate expression. The adsorption efficiency increased with increasing adsorbent dosage and contact time and reached equilibrium in 24 h. The equilibrium data showed better compliance with a Langmuir isotherm than a Freundlich isotherm. Effective removal of Cr(VI) was demonstrated at pH values ranging from 2 to 10. The adsorption capacity of Cr(VI) was found to be highest (82%) at pH 3.4 and greatly depended on the solution pH. We found that Cr(VI) adsorption decreased with increasing pH over the pH range of 3.4-10. The adsorption capacity increased dramatically when the temperature increased from 10 °C to 50 °C regardless of the amount of CNOs used. Cr(VI) removal decreased by ∼13% when Zn(II), Cu(II), and Pb(II) were present, while there were no significant changes observed when NO 3 - or SO 4 2- was present. The overall results support that CNOs can be used as an alternative adsorbent material to remove Cr(VI) in the water treatment industry. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Solubility of carbon dioxide in aqueous solutions of N-methyldiethanolamine and piperazine

    NARCIS (Netherlands)

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

    2008-01-01

    The thermodynamics of the piperazine (PZ) activated aqueous N-methyldiethanolamine (MDEA) are studied. New experimental equilibrium data are reported on the solublity of CO 2 into aqueous solutions of MDEA and PZ, which complement published experimental data. CO 2 solubilities and their

  2. 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

  3. Carbon nanotubes as solid-phase extraction sorbents prior to atomic spectrometric determination of metal species: A review

    Energy Technology Data Exchange (ETDEWEB)

    Herrero Latorre, C., E-mail: carlos.herrero@usc.es [Universidad de Santiago de Compostela, Dpto. Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias, Alfonso X el Sabio s/n, 27002 Lugo (Spain); Alvarez Mendez, J.; Barciela Garcia, J.; Garcia Martin, S.; Pena Crecente, R.M. [Universidad de Santiago de Compostela, Dpto. Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias, Alfonso X el Sabio s/n, 27002 Lugo (Spain)

    2012-10-24

    Highlights: Black-Right-Pointing-Pointer The use of CNTs as sorbent for metal species in solid phase extraction has been described. Black-Right-Pointing-Pointer Physical and chemical strategies for functionalization of carbon nanotubes have been discussed. Black-Right-Pointing-Pointer Published analytical methods concerning solid phase extraction and atomic spectrometric determination have been reviewed. - Abstract: New materials have significant impact on the development of new methods and instrumentation for chemical analysis. From the discovery of carbon nanotubes in 1991, single and multi-walled carbon nanotubes - due to their high adsorption and desorption capacities - have been employed as sorption substrates in solid-phase extraction for the preconcentration of metal species from diverse matrices. Looking for successive improvements in sensitivity and selectivity, in the past few years, carbon nanotubes have been utilized as sorbents for solid phase extraction in three different ways: like as-grown, oxidized and functionalized nanotubes. In the present paper, an overview of the recent trends in the use of carbon nanotubes for solid phase extraction of metal species in environmental, biological and food samples is presented. The determination procedures involved the adsorption of metals on the nanotube surface, their quantitative desorption and subsequent measurement by means of atomic spectrometric techniques such as flame atomic absorption spectrometry, electrothermal atomic absorption spectrometry or inductively coupled plasma atomic emission spectrometry/mass spectrometry, among others. Synthesis, purification and types of carbon nanotubes, as well as the diverse chemical and physical strategies for their functionalization are described. Based on 140 references, the performance and general properties of the applications of solid phase extraction based on carbon nanotubes for metal species atomic spectrometric determination are discussed.

  4. Uptake of Pb(II ion From Aqueous Solution Using Silk Cotton Hull Carbon: An Agricultural Waste Biomass

    Directory of Open Access Journals (Sweden)

    R. Shanmugavalli

    2006-01-01

    Full Text Available Activated carbon prepared from silk cotton hull (SCH was used for the adsorptive removal of Pb(II ion from aqueous solution. The raw material used for the preparation of activated carbon is the waste of agricultural product; the production of this carbon is expected to be economically feasible. Parameters such as agitation time, metal ion concentration, adsorbent dose, pH and Particle size were studied. Adsorption equilibrium was reached within 80 min for 10, 20, 30 and 40mg/l of Pb(II ion with 50mg of carbon per mL of solution. Adsorption parameters were determined using both Langmuir and Freundlich isotherm models. The adsorption efficiency reached 100% for 20, 30 and 40mg/l of Pb(II ion with 120, 140 and 150mg of carbon. Pb(II ion removal increased as the pH increased from 2 to 5 and remains constant up to pH 10. Desorption studies were also carried out with dilute hydrochloric acid to know the mechanism of adsorption. Quantitative desorption of Pb(II ion from carbon indicates that adsorption of metal ion is by ion-exchange. Efficiency of the adsorption of SCH was also studied with Pb containing industrial wastewater by varying pH and carbon concentration.

  5. Mechanisms for Olivine Carbonation at the Nili Fossae/Isidis Basin Boundary, Mars: Evidence of Intense Surface Aqueous Activity

    Science.gov (United States)

    Mustard, J. F.

    2015-12-01

    One of the most extensive surface deposits of carbonate on Mars is on the slopes of the Isidis Basin rising up to the Nili Fossae region (Ehlmann et al., 2008; Niles et al., 2012; Edwards and Ehlmann 2015). A key factor for the formation of carbonate in this region is the association of carbonate with olivine: this ubiquitous relationship shows the reactants and products are in direct association. There are four clear hypotheses for the geologic environment of formation. 1) Water-rock interaction in the shallow subsurface at slightly elevated temperatures altered olivine to Mg-carbonate perhaps through extended periods of heat and water with burial leading to olivine-serpentine-talc-chlorite alteration pathway (Brown et al., 2010; Viviano et al., 2013). 2) Olivine-rich material, heated by impact or volcanic processes, emplaced on top of a water-bearing phyllosilicate rich unit initiated hydrothermal alteration along the contact. 3) Olivine-rich rocks were weathered to carbonate at surface (cold) temperatures in a manner similar to olivine weathering of meteorites in Antarctica. 4) Carbonate precipitated from shallow ephemeral lakes. These hypotheses are quite different in their predictions of mineral assemblage, water requirements, and habitability. I will show new data and analyses that are providing insights to the question of the mineralogy and assemblages of carbonate-bearing units in the region, diagostic of processes. It is becoming more evident that surface aqueous activity, perhaps involving an extensive cryosphere in the form of Hesperian ice sheets.

  6. l-Tryptophan-capped carbon quantum dots for the sensitive and selective fluorescence detection of mercury ion in aqueous solution

    Science.gov (United States)

    Wan, Xuejuan; Li, Shifeng; Zhuang, Lulu; Tang, Jiaoning

    2016-07-01

    l-Tryptophan-capped carbon quantum dots ( l-CQDs) were facilely synthesized through "green" methodology, and the obtained material was utilized as a sensitive and selective fluorescence sensor for mercury ion (Hg2+) in pure aqueous solutions. Carboxyl-functionalized CQDs were first green synthesized by a one-step hydrothermal route, and l-tryptophan was then attached to CQDs via direct surface condensation reaction in aqueous solution at room temperature. The as-synthesized l-CQDs had an average size of ca. 5 nm with a good dispersity in water, and exhibited a favorable selectivity for Hg2+ ions over a range of other common metal cations in aqueous solution (10 mM PBS buffer, pH 6.0). Upon the addition of Hg2+, a complete fluorescence quenching (ON-OFF switching) of l-CQDs was evident from the fluorescence titration experiment, and the fluorescence detection limit of Hg2+ was calculated to be 11 nM, which indicated that the obtained environmentally friendly l-CQDs had sensitive detection capacity for Hg2+ in aqueous solution.

  7. l-Tryptophan-capped carbon quantum dots for the sensitive and selective fluorescence detection of mercury ion in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Wan, Xuejuan; Li, Shifeng; Zhuang, Lulu; Tang, Jiaoning, E-mail: tjn@szu.edu.cn [Shenzhen University, Shenzhen Key Laboratory of Special Functional Materials, College of Materials Science and Engineering (China)

    2016-07-15

    l-Tryptophan-capped carbon quantum dots (l-CQDs) were facilely synthesized through “green” methodology, and the obtained material was utilized as a sensitive and selective fluorescence sensor for mercury ion (Hg{sup 2+}) in pure aqueous solutions. Carboxyl-functionalized CQDs were first green synthesized by a one-step hydrothermal route, and l-tryptophan was then attached to CQDs via direct surface condensation reaction in aqueous solution at room temperature. The as-synthesized l-CQDs had an average size of ca. 5 nm with a good dispersity in water, and exhibited a favorable selectivity for Hg{sup 2+} ions over a range of other common metal cations in aqueous solution (10 mM PBS buffer, pH 6.0). Upon the addition of Hg{sup 2+}, a complete fluorescence quenching (ON–OFF switching) of l-CQDs was evident from the fluorescence titration experiment, and the fluorescence detection limit of Hg{sup 2+} was calculated to be 11 nM, which indicated that the obtained environmentally friendly l-CQDs had sensitive detection capacity for Hg{sup 2+} in aqueous solution.

  8. 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.

  9. Size, shape, and internal atomic ordering of nanocrystals by atomic pair distribution functions: a comparative study of gamma-Fe2O3 nanosized spheres and tetrapods.

    Science.gov (United States)

    Petkov, Valeri; Cozzoli, P Davide; Buonsanti, Raffaella; Cingolani, Roberto; Ren, Yang

    2009-10-14

    Due to their limited length of structural coherence nanocrystalline materials show very diffuse powder X-ray diffraction patterns that are difficult to interpret unambiguously. We demonstrate that a combination of high-energy X-ray powder diffraction and atomic pair distribution function analysis can be used to both assess the geometry (i.e., size and shape) and determine the internal atomic ordering of nanocrystalline materials in a straightforward way. As an example we consider cubic gamma-Fe(2)O(3) nanosized crystals shaped as spheres and tetrapods.

  10. Atomic Structures of Graphene, Benzene and Methane with Bond Lengths as Sums of the Single, Double and Resonance Bond Radii of Carbon

    OpenAIRE

    Heyrovska, Raji

    2008-01-01

    Two dimensional layers of graphene are currently drawing a great attention in fundamental and applied nanoscience. Graphene consists of interconnected hexagons of carbon atoms as in graphite. This article presents for the first time the structures of graphene at the atomic level and shows how it differs from that of benzene, due to the difference in the double bond and resonance bond based radii of carbon. The carbon atom of an aliphatic compound such as methane has a longer covalent single b...

  11. Experimental Investigation Of Segregation Of Carbon Atoms Due To Sub-Zero Cryogenic Treatment In Cold Work Tool Steel By Mechanical Spectroscopy And Atom Probe Tomography

    Directory of Open Access Journals (Sweden)

    Min N.

    2015-06-01

    Full Text Available In this work, we present mechanical spectroscopy of cold work tool steel subjected to sub-zero cryogenic soaking treatment to reveal the carbon segregation and the subsequent carbides refinement. The maximum of Snoek-Köster (SK peak height was obtained in the sample subjected to soaking 1h at −130°C cryogenic treatment. The SK peak height is reduced with prolonging the soaking time. The results indicate that an increase in the height of SK peak is connected with an increase in dislocation density and the number of segregated carbon atoms in the vicinity of dislocations or twin planes after martensite transformation at −130°C which is confirmed by corresponding TEM and atom probe tomography measurement. Hence, it is suggested that the isothermal martensite, formed during the cryogenic soaking treatment decreases (APT the height of SK peak.

  12. 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.

  13. 75 FR 6070 - Notice of Public Meeting on the International Atomic Energy Agency Basic Safety Standards Version...

    Science.gov (United States)

    2010-02-05

    ... COMMISSION Notice of Public Meeting on the International Atomic Energy Agency Basic Safety Standards Version 3.0, Draft Safety Requirements DS379 AGENCY: Nuclear Regulatory Commission. ACTION: Notice of Public... open forum with the public and other stakeholders on a revision to the International Basic Safety...

  14. Atomic-Layer-Deposition Functionalized Carbonized Mesoporous Wood Fiber for High Sulfur Loading Lithium Sulfur Batteries.

    Science.gov (United States)

    Luo, Chao; Zhu, Hongli; Luo, Wei; Shen, Fei; Fan, Xiulin; Dai, Jiaqi; Liang, Yujia; Wang, Chunsheng; Hu, Liangbing

    2017-05-03

    Lithium-sulfur battery (LSB) as one of the most promising energy storage devices suffers from poor conductivity of sulfur and fast capacity decay triggered by the dissolution of polysulfides. In this work, functionalized carbonized mesoporous wood fiber (f-CMWF) is employed as a host to accommodate sulfur for the first time. Natural wood microfiber has unique hierarchical and mesoporous structure, which is well-maintained after carbonization. With such a hierarchical mesoporous structure, a high sulfur loading of 76 wt % is achieved in CMWF electrodes. The pore size of CMWF is tunable by atomic layer deposition (ALD) of a 5 nm Al 2 O 3 coating to form the f-CMWF. Such a thin layer slightly decreases the sulfur loading to 70%, but it remarkably promotes the cyclic stability of sulfur cathode, which delivers an initial capacity of 1115 mAh g -1 , and maintains a reversible capacity of 859 mAh g -1 for 450 cycles, corresponding to a slow capacity decay rate of 0.046% per cycle. More importantly, natural wood microfiber is first used as a raw material for sulfur encapsulating. This work is also critical for using low cost and mesoporous biomass carbon as bifunctional scaffold for LSB.

  15. Electron-beam-induced carbon contamination on silicon: characterization using Raman spectroscopy and atomic force microscopy.

    Science.gov (United States)

    Lau, Deborah; Hughes, Anthony E; Muster, Tim H; Davis, Timothy J; Glenn, A Matthew

    2010-02-01

    Electron-beam-induced carbon film deposition has long been recognized as a side effect of scanning electron microscopy. To characterize the nature of this type of contamination, silicon wafers were subjected to prolonged exposure to 15 kV electron beam energy with a probe current of 300 pA. Using Raman spectroscopy, the deposited coating was identified as an amorphous carbon film with an estimated crystallite size of 125 A. Using atomic force microscopy, the cross-sectional profile of the coating was found to be raised and textured, indicative of the beam raster pattern. A map of the Raman intensity across the coating showed increased intensity along the edges and at the corner of the film. The intensity profile was in excess of that which could be explained by thickness alone. The enhancement was found to correspond with a modeled local field enhancement induced by the coating boundary and showed that the deposited carbon coating generated a localized disturbance in the opto-electrical properties of the substrate, which is compared and contrasted with Raman edge enhancement that is produced by surface structure in silicon.

  16. Simple-Cubic Carbon Frameworks with Atomically Dispersed Iron Dopants toward High-Efficiency Oxygen Reduction.

    Science.gov (United States)

    Wang, Biwei; Wang, Xinxia; Zou, Jinxiang; Yan, Yancui; Xie, Songhai; Hu, Guangzhi; Li, Yanguang; Dong, Angang

    2017-03-08

    Iron and nitrogen codoped carbons (Fe-N-C) have attracted increasingly greater attention as electrocatalysts for oxygen reduction reaction (ORR). Although challenging, the synthesis of Fe-N-C catalysts with highly dispersed and fully exposed active sites is of critical importance for improving the ORR activity. Here, we report a new type of graphitic Fe-N-C catalysts featuring numerous Fe single atoms anchored on a three-dimensional simple-cubic carbon framework. The Fe-N-C catalyst, derived from self-assembled Fe 3 O 4 nanocube superlattices, was prepared by in situ ligand carbonization followed by acid etching and ammonia activation. Benefiting from its homogeneously dispersed and fully accessible active sites, highly graphitic nature, and enhanced mass transport, our Fe-N-C catalyst outperformed Pt/C and many previously reported Fe-N-C catalysts for ORR. Furthermore, when used for constructing the cathode for zinc-air batteries, our Fe-N-C catalyst exhibited current and power densities comparable to those of the state-of-the-art Pt/C catalyst.

  17. Mechanism of DNA cleavage by cationic manganese porphyrins: hydroxylations at the 1'-carbon and 5'-carbon atoms of deoxyriboses as initial damages.

    OpenAIRE

    Pratviel, G; Pitié, M.; Bernadou, J.; Meunier, B

    1991-01-01

    Cationic manganese-porphyrin complexes, free or targetted with an intercalating agent, are able to cleave DNA using oxygen atom donors like potassium monopersulfate or magnesium monoperphthalate as coreactants. Detailed studies of the cleavage of calf thymus DNA, before and after a heating step, show that free bases and 5-methylene-2-furanone are the main reaction products, indicating that hydroxylation at the 1'-carbon atom is the main target of these chemical agents. These data confirm that...

  18. 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. Copyright © 2016 Elsevier Inc. All rights reserved.

  19. Energy of the Isolated Metastable Iron-Nickel FCC Nanocluster with a Carbon Atom in the Tetragonal Interstice.

    Science.gov (United States)

    Bondarenko, Natalya V; Nedolya, Anatoliy V

    2017-12-01

    The energy of the isolated iron-nickel nanocluster was calculated by molecular mechanics method using Lennard-Jones potential. The cluster included a carbon atom that drifted from an inside octahedral interstice to a tetrahedral interstice in [Formula: see text] direction and after that in direction to the surface. In addition, one of 14 iron atoms was replaced by a nickel atom, the position of which was changing during simulation.The energy of the nanocluster was estimated at the different interatomic distances. As a result of simulation, the optimal interatomic distances of Fe-Ni-C nanocluster was chosen for the simulation, in which height of the potential barrier was maximal and face-centered cubic (FCC) nanocluster was the most stable.It is shown that there were three main positions of a nickel atom that significantly affected nanocluster's energy.The calculation results indicated that position of the carbon atom in the octahedral interstice was more energetically favorable than tetrahedral interstice in the case of FCC nanocluster. On the other side, the potential barrier was smaller in the direction [Formula: see text] than in the direction .This indicates that there are two ways for carbon atom to drift to the surface of the nanocluster.

  20. DFT study of Fe-Ni core-shell nanoparticles: stability, catalytic activity, and interaction with carbon atom for single-walled carbon nanotube growth.

    Science.gov (United States)

    Yang, Zhimin; Wang, Qiang; Shan, Xiaoye; Li, Wei-qi; Chen, Guang-hui; Zhu, Hongjun

    2015-02-21

    Metal catalysts play an important role in the nucleation and growth of single-walled carbon nanotubes (SWCNTs). It is essential for probing the nucleation and growth mechanism of SWCNTs to fundamentally understand the properties of the metal catalysts and their interaction with carbon species. In this study, we systematically studied the stability of 13- and 55-atom Fe and Fe-Ni core-shell particles as well as these particles interaction with the carbon atoms using the density functional theory calculations. Icosahedral 13- and 55-atom Fe-Ni core-shell bimetallic particles have higher stability than the corresponding monometallic Fe and Ni particles. Opposite charge transfer (or distribution) in these particles leads to the Fe surface-shell displays a positive charge, while the Ni surface-shell exhibits a negative charge. The opposite charge transfer would induce different chemical activities. Compared with the monometallic Fe and Ni particles, the core-shell bimetallic particles have weaker interaction with C atoms. More importantly, C atoms only prefer staying on the surface of the bimetallic particles. In contrast, C atoms prefer locating into the subsurface of the monometallic particles, which is more likely to form stable metal carbides. The difference of the mono- and bimetallic particles on this issue may result in different nucleation and growth mechanism of SWCNTs. Our findings provide useful insights for the design of bimetallic catalysts and a better understanding nucleation and growth mechanism of SWCNTs.

  1. X-ray photoelectron spectroscopy study of the functionalization of carbon metal-containing nanotubes with phosphorus atoms

    Energy Technology Data Exchange (ETDEWEB)

    Shabanova, I.N., E-mail: xps@fti.udm.ru; Terebova, N.S.

    2013-08-15

    Highlights: •Carbon metal-containing nanotubes (Me–Cu, Ni, Fe) were functionalized with chemical groups containing different concentrations of phosphorous. •The C1s and Me3s spectra were measured by the X-ray photoelectron spectroscopy method. •The values of the atomic magnetic moment of the carbon metal-containing nanotubes were determined. -- Abstract: In the present paper, carbon metal-containing (Me: Cu, Ni, Fe) nanotubes functionalized with phosphorus atoms (ammonium polyphosphate) were studied by X-ray photoelectron spectroscopy (XPS) on an X-ray electron magnetic spectrometer. It is found that the functionalization leads to the change of the metal atomic magnetic moment, i.e. the value of the atomic magnetic moment in the functionalized carbon metal-containing (Cu, Ni, Fe) nanotubes increases and is higher than that in pristine nanotubes. It is shown that the covalent bond of Me and P atoms is formed. This leads to an increase in the activity of the nanostructure surface which is necessary for the modification of materials.

  2. 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

  3. Dispersion C3 coefficients for the alkali-metal atoms interacting with a graphene layer and with a carbon nanotube

    CERN Document Server

    Arora, Bindiya; Sahoo, B K

    2013-01-01

    We evaluate separation dependent van der Waal dispersion ($C_3$) coefficients for the interactions of the Li, Na, K and Rb alkali atoms with a graphene layer and with a single walled carbon nanotube (CNT) using the hydrodynamic and Dirac models. The results from both the models are evaluated using accurate values of the dynamic polarizabilities of the above atoms. Accountability of these accurate values of dynamical polarizabilities of the alkali atoms in determination of the above $C_3$ coefficients are accentuated by comparing them with the coefficients evaluated using the dynamic dipole polarizabilities estimated from the single oscillator approximation which are typically employed in the earlier calculations. For practical description of the atom-surface interaction potentials the radial dependent $C_3$ coefficients are given for a wide range of separation distances between the ground states of the considered atoms and the wall surfaces and also for different values of nanotube radii. The coefficients for...

  4. The Effect of Atom Vacancy Defect on the Vibrational Behavior of Single-Walled Carbon Nanotubes: A Structural Mechanics Approach

    Directory of Open Access Journals (Sweden)

    S. K. Georgantzinos

    2014-04-01

    Full Text Available An atomistic structural mechanics method, which is based on the exclusive use of spring elements, is developed in order to study the effect of imperfections due to atom vacancy on the vibrational characteristics of single-walled carbon nanotubes (SWCNTs. The developed elements simulate the relative translations and rotations between atoms as well as the mass of the atoms. In this way, molecular mechanics theory can be applied directly because the atomic bonds are modeled by using exclusively physical variables such as bond stretching. The method is validated for its predictability comparing with vibration results found in the open literature for pristine nanotubes. Then, it is used for the vibration analysis of defective nanotubes. Imperfections such as one-atom vacancy, two-atom vacancy, and one carbon hexagonal cell vacancy are investigated. Their effect on vibrational behavior is explored for different defect positions, nanotube diameters, and support conditions. According to the obtained results, the fundamental frequency is decreased as the size of imperfection increases, and the percentage reduction in fundamental frequency due to the atomic vacancy defect is more affected for a single-clamped SWCNT than for a double-clamped one.

  5. Synthesis of magnetic nanoporous carbon from metal-organic framework for the fast removal of organic dye from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Jiao, Caina; Wang, Yanen; Li, Menghua; Wu, Qiuhua; Wang, Chun; Wang, Zhi, E-mail: wangzhi@hebau.edu.cn

    2016-06-01

    In this paper, a magnetic nanoporous carbon (Fe{sub 3}O{sub 4}/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 N{sub 2} adsorption–desorption isotherms. The Fe{sub 3}O{sub 4}/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 Fe{sub 3}O{sub 4}/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 Fe{sub 3}O{sub 4}/NPC can be used as a good alternative for the effective removal of organic dyes from wastewater. - Highlights: • Fe{sub 3}O{sub 4}/NPC nanocomposite was synthesized by choosing MOF-5 as carbon precursor. • Fe{sub 3}O{sub 4}/NPC was used as an adsorbent for removal of organic dye from aqueous solution. • Fe{sub 3}O{sub 4}/NPC could be a promising candidate for pollutants removal.

  6. Adsorptive removal of phenol from aqueous solutions on activated carbon prepared from tobacco residues: Equilibrium, kinetics and thermodynamics

    Energy Technology Data Exchange (ETDEWEB)

    Kilic, Murat; Apaydin-Varol, Esin [Department of Chemical Engineering, Anadolu University, Eskisehir 26470 (Turkey); Puetuen, Ayse E., E-mail: aeputun@anadolu.edu.tr [Department of Chemical Engineering, Anadolu University, Eskisehir 26470 (Turkey)

    2011-05-15

    This study consists of producing high surface area activated carbon from tobacco residues by chemical activation and its behavior of phenol removal from aqueous solutions. K{sub 2}CO{sub 3} and KOH were used as chemical activation agents and three impregnation ratios (50, 75 and 100 wt.%) were applied on biomass. Maximum BET surface areas of activated carbons were obtained from impregnation with 75 wt.% of K{sub 2}CO{sub 3} and 75 wt.% of KOH as 1635 and 1474 m{sup 2}/g, respectively. Optimum adsorption conditions were determined as a function of pH, adsorbent dosage, initial phenol concentration, contact time and temperature of solution for phenol removal. To describe the equilibrium isotherms the experimental data were analyzed by the Langmuir, Freundlich, Dubinin-Radushkevich (D-R) and Temkin isotherm models. Pseudo-first order, pseudo-second order and intraparticle diffusion kinetic models were used to find out the kinetic parameters and mechanism of adsorption process. The thermodynamic parameters such as {Delta}G{sup o}, {Delta}H{sup o} and {Delta}S{sup o} were calculated for predicting the nature of adsorption. According to the experimental results, activated carbon prepared from tobacco residue seems to be an effective, low-cost and alternative adsorbent precursor for the removal of phenol from aqueous solutions.

  7. Single-walled carbon nanotubes coated with ZnO by atomic layer deposition

    Science.gov (United States)

    Pal, Partha P.; Gilshteyn, Evgenia; Jiang, Hua; Timmermans, Marina; Kaskela, Antti; Tolochko, Oleg V.; Kurochkin, Alexey V.; Karppinen, Maarit; Nisula, Mikko; Kauppinen, Esko I.; Nasibulin, Albert G.

    2016-12-01

    The possibility of ZnO deposition on the surface of single-walled carbon nanotubes (SWCNTs) with the help of an atomic layer deposition (ALD) technique was successfully demonstrated. The utilization of pristine SWCNTs as a support resulted in a non-uniform deposition of ZnO in the form of nanoparticles. To achieve uniform ZnO coating, the SWCNTs first needed to be functionalized by treating the samples in a controlled ozone atmosphere. The uniformly ZnO coated SWCNTs were used to fabricate UV sensing devices. An UV irradiation of the ZnO coated samples turned them from hydrophobic to hydrophilic behaviour. Furthermore, thin films of the ZnO coated SWCNTs allowed us switch p-type field effect transistors made of pristine SWCNTs to have ambipolar characteristics.

  8. Modeling and optimization of atomic layer deposition processes on vertically aligned carbon nanotubes

    Directory of Open Access Journals (Sweden)

    Nuri Yazdani

    2014-03-01

    Full Text Available Many energy conversion and storage devices exploit structured ceramics with large interfacial surface areas. Vertically aligned carbon nanotube (VACNT arrays have emerged as possible scaffolds to support large surface area ceramic layers. However, obtaining conformal and uniform coatings of ceramics on structures with high aspect ratio morphologies is non-trivial, even with atomic layer deposition (ALD. Here we implement a diffusion model to investigate the effect of the ALD parameters on coating kinetics and use it to develop a guideline for achieving conformal and uniform thickness coatings throughout the depth of ultra-high aspect ratio structures. We validate the model predictions with experimental data from ALD coatings of VACNT arrays. However, the approach can be applied to predict film conformality as a function of depth for any porous topology, including nanopores and nanowire arrays.

  9. Electrical tomography using atomic force microscopy and its application towards carbon nanotube-based interconnects.

    Science.gov (United States)

    Schulze, A; Hantschel, T; Dathe, A; Eyben, P; Ke, X; Vandervorst, W

    2012-08-03

    The fabrication and integration of low-resistance carbon nanotubes (CNTs) for interconnects in future integrated circuits requires characterization techniques providing structural and electrical information at the nanometer scale. In this paper we present a slice-and-view approach based on electrical atomic force microscopy. Material removal achieved by successive scanning using doped ultra-sharp full-diamond probes, manufactured in-house, enables us to acquire two-dimensional (2D) resistance maps originating from different depths (equivalently different CNT lengths) on CNT-based interconnects. Stacking and interpolating these 2D resistance maps results in a three-dimensional (3D) representation (tomogram). This allows insight from a structural (e.g. size, density, distribution, straightness) and electrical point of view simultaneously. By extracting the resistance evolution over the length of an individual CNT we derive quantitative information about the resistivity and the contact resistance between the CNT and bottom electrode.

  10. Electrochemical behavior of adrenaline at the carbon atom wire modified electrode

    Science.gov (United States)

    Xue, Kuan-Hong; Liu, Jia-Mei; Wei, Ri-Bing; Chen, Shao-Peng

    2006-09-01

    Electrochemical behavior of adrenaline at an electrode modified by carbon atom wires (CAWs), a new material, was investigated by cyclic voltammetry combined with UV-vis spectrometry, and forced convection method. As to the electrochemical response of redox of adrenaline/adrenalinequinone couple in 0.50 M H 2SO 4, at a nitric acid treated CAW modified electrode, the anodic and cathodic peak potentials Epa and Epc shifted by 87 mV negatively and 139 mV in the positive direction, respectively, and standard heterogeneous rate constant k0 increased by 16 times compared to the corresponding bare electrode, indicating the extraordinary activity of CAWs in electrocatalysis for the process.

  11. Electrochemical behavior of adrenaline at the carbon atom wire modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Xue Kuanhong [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China)], E-mail: khxue@njnu.edu.cn; Liu Jiamei [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China); Wei Ribing [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China); Chen Shaopeng [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China)

    2006-09-11

    Electrochemical behavior of adrenaline at an electrode modified by carbon atom wires (CAWs), a new material, was investigated by cyclic voltammetry combined with UV-vis spectrometry, and forced convection method. As to the electrochemical response of redox of adrenaline/adrenalinequinone couple in 0.50 M H{sub 2}SO{sub 4}, at a nitric acid treated CAW modified electrode, the anodic and cathodic peak potentials E {sub pa} and E {sub pc} shifted by 87 mV negatively and 139 mV in the positive direction, respectively, and standard heterogeneous rate constant k {sup 0} increased by 16 times compared to the corresponding bare electrode, indicating the extraordinary activity of CAWs in electrocatalysis for the process.

  12. 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)

  13. Method for aqueous gold thiosulfate extraction using copper-cyanide pretreated carbon adsorption

    Science.gov (United States)

    Young, Courtney; Melashvili, Mariam; Gow, Nicholas V

    2013-08-06

    A gold thiosulfate leaching process uses carbon to remove gold from the leach liquor. The activated carbon is pretreated with copper cyanide. A copper (on the carbon) to gold (in solution) ratio of at least 1.5 optimizes gold recovery from solution. To recover the gold from the carbon, conventional elution technology works but is dependent on the copper to gold ratio on the carbon.

  14. Negotiating supranational rules - The genesis of the International Atomic Energy Agency Safeguards System

    Energy Technology Data Exchange (ETDEWEB)

    Forland, Astrid

    1998-12-31

    The object of this thesis 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 evolution is traced not through the practical implementation of the safeguards system, but through the various multilateral negotiations through which it was created. The focus is on analysing the arguments advanced in the various negotiations, and the main objective is to single out the factors determining the result. The discussion is organised into the following chapters: (1) The statute of the IAEA, (2) The IAEA 1961 safeguard document (INFCIRC/26), (3) The IAEA 1965 safeguards document (INFCIRC/66), (4) The non-proliferation treaty, (5) NPT safeguards. 92 refs.

  15. Understanding the Atomic Scale Mechanisms that Control the Attainment of Ultralow Friction and Wear in Carbon-Based Materials

    Science.gov (United States)

    2016-01-16

    2015. 15. Invited. New Insights into Friction and Wear through In-Situ Nanotribology. Joint Symposium of the Surface Science Society of Japan and...and Carpick, R.W. Influence of Surface Passivation on the Friction and Wear Behavior of Ultrananocrystalline Diamond and Tetrahedral Amorphous Carbon...AFRL-AFOSR-JP-TR-2016-0053 Understanding the Atomic Scale Mechanism that controls the attainment of ultralow friction and wear in carbon based

  16. Selenium analysis by an integrated microwave digestion-needle trap device with hydride sorption on carbon nanotubes and electrothermal atomic absorption spectrometry determination

    Science.gov (United States)

    Maratta Martínez, Ariel; Vázquez, Sandra; Lara, Rodolfo; Martínez, Luis Dante; Pacheco, Pablo

    2018-02-01

    An integrated microwave assisted digestion (MW-AD) - needle trap device (NTD) for selenium determination in grape pomace samples is presented. The NTD was filled with oxidized multiwall carbon nanotubes (oxMWCNTS) where Se hydrides were preconcentrated. Determination was carried out by flow injection-electrothermal atomic absorption spectrometry (FI-ETAAS). The variables affecting the system were established by a multivariate design (Plackett Burman), indicating that the following variables significantly affect the system: sample amount, HNO3 digestion solution concentration, NaBH4 volume and elution volume. A Box-Behnken design was implemented to determine the optimized values of these variables. The system improved Se atomization in the graphite furnace, since only trapped hydrides reached the graphite furnace, and the pyrolysis stage was eliminated according to the aqueous matrix of the eluate. Under optimized conditions the system reached a limit of quantification of 0.11 μg kg- 1, a detection limit of 0.032 μg kg- 1, a relative standard deviation of 4% and a preconcentration factor (PF) of 100, reaching a throughput sample of 5 samples per hour. Sample analysis show Se concentrations between 0.34 ± 0.03 μg kg- 1 to 0.48 ± 0.03 μg kg- 1 in grape pomace. This system provides minimal reagents and sample consumption, eliminates discontinuous stages between samples processing reaching a simpler and faster Se analysis.

  17. Aqueous extracts of mango and orange peel as green inhibitors for carbon steel in hydrochloric acid solution

    OpenAIRE

    Rocha, Janaina Cardozo da; Gomes, José Antônio da Cunha Ponciano; D'Elia, Eliane

    2014-01-01

    In this paper, aqueous extracts of mango and orange peels were shown to be good corrosion inhibitors for carbon steel in a 1 mol L- 1 HCl solution. The inhibition efficiency increased as the extract concentration increased over a concentration range of 200-600 mg L- 1, varying from 79 to 96% (mango) and 84 to 91% (orange) using Tafel plots and from 69 to 94% (mango) and 76 to 90% (orange) using electrochemical impedance. In the presence of 400 mg L- 1 of mango and orange peel ...

  18. 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

  19. 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.

  20. Evaluation of carbons derived from Gingelly oil cake for the removal of lead(II) from aqueous solutions.

    Science.gov (United States)

    Nagashanmugam, K B; Srinivasan, K

    2010-10-01

    The adsorption of lead(II) onto activated carbons prepared from Gingelly Oil Cake (GOC) by using thermal, sulphuric and zinc chloride activations was investigated. The effects of experimental parameters such as pH, initial concentration, contact time and adsorbents dosage on the lead(II) removal were studied. The data were fitted with Langmuir, Freundlich and Temkin models to describe the equilibrium isotherms. The kinetic data fitted well with Lagergren pseudo first order and pseudo second order models. The maximum adsorption capacity for lead(II) on adsorbents calculated from Langmuir isotherm was found to be 105.26 mg/g and 114.94 mg/g for thermally activated and sulphuric acid activated carbons respectively. R2 values show that Langmuir model fits best to sulphuric acid activated carbon and Freundlich model fits best to thermally activated and zinc chloride activated carbons. The kinetic rates were best fitted to pseudo second order model. FT-IR analysis was used to obtain information on the nature of possible interaction between adsorbents and metal ions. SEM images confirmed the adsorption of lead(II) onto GOC adsorbents through morphological observations. Thermodynamic study showed the feasibility of process and spontaneous nature of the adsorption. The adsorbents were also tested for the removal of lead(II) from lead battery synthetic wastewater. The results indicate that carbons derived from GOC could be used to effectively adsorb lead(II) from aqueous solutions and wastewaters.

  1. Boosting the local anodic oxidation of silicon through carbon nanofiber atomic force microscopy probes

    Directory of Open Access Journals (Sweden)

    Gemma Rius

    2015-01-01

    Full Text Available Many nanofabrication methods based on scanning probe microscopy have been developed during the last decades. Local anodic oxidation (LAO is one of such methods: Upon application of an electric field between tip and surface under ambient conditions, oxide patterning with nanometer-scale resolution can be performed with good control of dimensions and placement. LAO through the non-contact mode of atomic force microscopy (AFM has proven to yield a better resolution and tip preservation than the contact mode and it can be effectively performed in the dynamic mode of AFM. The tip plays a crucial role for the LAO-AFM, because it regulates the minimum feature size and the electric field. For instance, the feasibility of carbon nanotube (CNT-functionalized tips showed great promise for LAO-AFM, yet, the fabrication of CNT tips presents difficulties. Here, we explore the use of a carbon nanofiber (CNF as the tip apex of AFM probes for the application of LAO on silicon substrates in the AFM amplitude modulation dynamic mode of operation. We show the good performance of CNF-AFM probes in terms of resolution and reproducibility, as well as demonstration that the CNF apex provides enhanced conditions in terms of field-induced, chemical process efficiency.

  2. One-pot synthesis of carbon-coated nanosized LiTi2(PO4)3 as anode materials for aqueous lithium ion batteries

    Science.gov (United States)

    Liu, Zhantao; Qin, Xusong; Xu, Hui; Chen, Guohua

    2015-10-01

    In this study, a one-pot sintering process incorporating sol-gel preparation route and in-situ carbon coating was proposed for the synthesis of carbon-coated nanosized LiTi2(PO4)3. Experimental results show that the prepared LiTi2(PO4)3 particles are of high crystallinity and well-coated by turbostratic carbon. Attributed to nanosized particles and enhanced conductivity provided by turbostratic carbon coating, the carbon-coated LiTi2(PO4)3 showed high rate performance and good cycling life in aqueous electrolyte. Particularly, the carbon-coated LiTi2(PO4)3 exhibited initial specific capacities of 103 and 89 mAh g-1, and retained 80.6% and 97% of the initial capacities after 120 cycles at 1C and 10C in aqueous electrolyte, respectively. The high rate performance and good cycling life of carbon-coated LiTi2(PO4)3 in aqueous electrolyte reveal its potential as negative electrode in aqueous lithium-ion batteries for electric vehicles and industrial-scale energy storage systems.

  3. Biosorption of formic and acetic acids from aqueous solution using activated carbon from shea butter seed shells

    Science.gov (United States)

    Adekola, Folahan A.; Oba, Ismaila A.

    2017-10-01

    The efficiency of prepared activated carbon from shea butter seed shells (SB-AC) for the adsorption of formic acid (FA) and acetic acid (AA) from aqueous solution was investigated. The effect of optimization parameters including initial concentration, agitation time, adsorbent dosage and temperature of adsorbate solution on the sorption capacity were studied. The SB-AC was characterized for the following parameters: bulk density, moisture content, ash content, pH, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The optimal conditions for the adsorption were established and the adsorption data for AA fitted Dubinin-Radushkevich (D-R) isotherm well, whereas FA followed Langmuir isotherm. The kinetic data were examined. It was found that pseudo-second-order kinetic model was found to adequately explain the sorption kinetic of AA and FA from aqueous solution. It was again found that intraparticle diffusion was found to explain the adsorption mechanism. Adsorption thermodynamic parameters were estimated and the negative values of Δ G showed that the adsorption process was feasible and spontaneous in nature, while the negative values of Δ H indicate that the adsorption process was exothermic. It is therefore established that SB-AC has good potential for the removal of AA and FA from aqueous solution. Hence, it should find application in the regular treatment of polluted water in aquaculture and fish breeding system.

  4. Thermal MEMS actuator operation in aqueous media/seawater: Performance enhancement through atomic layer deposition post processing of PolyMUMPs devices

    Energy Technology Data Exchange (ETDEWEB)

    Warnat, Stephan, E-mail: stephan.warnat@dal.ca; Forbrigger, Cameron; Hubbard, Ted [Mechanical Engineering, Dalhousie University, Halifax, Nova Scotia B3J 2X4 (Canada); Bertuch, Adam; Sundaram, Ganesh [Ultratech Inc., Waltham, Massachusetts 02453 (United States)

    2015-01-15

    A method to enhance thermal microelectromechanical systems (MEMS) actuators in aqueous media by using dielectric encapsulation layers is presented. Aqueous media reduces the available mechanical energy of the thermal actuator through an electrical short between actuator structures. Al{sub 2}O{sub 3} and TiO{sub 2} laminates with various thicknesses were deposited on packaged PolyMUMPs devices to electrically separate the actuator from the aqueous media. Atomic layer deposition was used to form an encapsulation layer around released MEMS structures and the package. The enhancement was assessed by the increase of the elastic energy, which is proportional to the mechanical stiffness of the actuator and the displacement squared. The mechanical stiffness of the encapsulated actuators compared with the noncoated actuators was increased by factors ranging from 1.45 (for 45 nm Al{sub 2}O{sub 3} + 20 nm TiO{sub 2}) to 1.87 (for 90 nm Al{sub 2}O{sub 3} + 40 nm TiO{sub 2}). Displacement measurements were made for all laminate combinations in filtered tap water and seawater by using FFT based displacement measurement technique with a repeatability of ∼10 nm. For all laminate structures, the elastic energy increased and enhanced the actuator performance: In seawater, the mechanical output energy increased by factors ranging from 5 (for 90 nm Al{sub 2}O{sub 3}) to 11 (for 90 nm Al{sub 2}O{sub 3} + 40 nm TiO{sub 2}). The authors also measured the long-term actuator stability/reliability in seawater. Samples were stored for 29 days in seawater and tested for 17 days in seawater. Laminates with TiO{sub 2} layers allowed constant operation over the entire measurement period.

  5. Development of novel and sensitive methods for the determination of sulfide in aqueous samples by hydrogen sulfide generation-inductively coupled plasma-atomic emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Colon, M. [Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain); Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Todoli, J.L. [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Hidalgo, M. [Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain); Iglesias, M. [Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain)], E-mail: monica.iglesias@udg.es

    2008-02-25

    Two new, simple and accurate methods for the determination of sulfide (S{sup 2-}) at low levels ({mu}g L{sup -1}) in aqueous samples were developed. The generation of hydrogen sulfide (H{sub 2}S) took place in a coil where sulfide reacted with hydrochloric acid. The resulting H{sub 2}S was then introduced as a vapor into an inductively coupled plasma-atomic emission spectrometer (ICP-AES) and sulfur emission intensity was measured at 180.669 nm. In comparison to when aqueous sulfide was introduced, the introduction of sulfur as H{sub 2}S enhanced the sulfur signal emission. By setting a gas separator at the end of the reaction coil, reduced sulfur species in the form of H{sub 2}S were removed from the water matrix, thus, interferences could be avoided. Alternatively, the gas separator was replaced by a nebulizer/spray chamber combination to introduce the sample matrix and reagents into the plasma. This methodology allowed the determination of both sulfide and sulfate in aqueous samples. For both methods the linear response was found to range from 5 {mu}g L{sup -1} to 25 mg L{sup -1} of sulfide. Detection limits of 5 {mu}g L{sup -1} and 6 {mu}g L{sup -1} were obtained with and without the gas separator, respectively. These new methods were evaluated by comparison to the standard potentiometric method and were successfully applied to the analysis of reduced sulfur species in environmental waters.

  6. 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.

  7. Polymer binding to carbon nanotubes in aqueous dispersions: residence time on the nanotube surface as obtained by NMR diffusometry.

    Science.gov (United States)

    Frise, Anton E; Pagès, Guilhem; Shtein, Michael; Pri Bar, Ilan; Regev, Oren; Furó, István

    2012-03-08

    The binding of block copolymer Pluronic F-127 in aqueous dispersions of single- (SWCNT) and multiwalled (MWCNT) carbon nanotubes has been studied by pulsed-field-gradient (PFG) (1)H NMR spectroscopy. We show that a major fraction of polymers exist as a free species while a minor fraction is bound to the carbon nanotubes (CNT). The polymers exchange between these two states with residence times on the nanotube surface of 24 ± 5 ms for SWCNT and of 54 ± 11 ms for MWCNT. The CNT concentration in the solution was determined by improved thermal gravimetric analysis (TGA) indicating that the concentration of SWCNT dispersed by F-127 was significantly higher than that for MWCNT. For SWCNT, the area per adsorbed Pluronic F-127 molecule is estimated to be about 40 nm(2).

  8. Kinetic Approach for the Adsorption of Organophosphorous Pesticides from Aqueous Solution Using “Waste” Jute Fiber Carbon

    Directory of Open Access Journals (Sweden)

    S. Senthilkumaar

    2010-01-01

    Full Text Available Chemically activated “Waste” Jute Fiber carbon has been effectively used for the removal of five organophosphorous pesticides (malathion, monocrotophos, methylparathion, phosphamidon and dimethoate from aqueous solutions. The prepared activated jute fiber carbon was characterized by using Elemental analyzer and proximate analysis methods. The adsorption equilibrium was examined at 28 ºC. Three different kinetic models, the pseudo first order, pseudo second order and Elovich kinetic models were selected to analyses the adsorption process. To compare the fitness of pseudo first order and pseudo second order, sum of the squares of the errors and correlation coefficient, r2 values were calculated. The Elovich model was used to confirm the chemisorptions.

  9. Studies of single walled carbon nanotubes for biomedical, mechanical and electrical applications using atomic force microscopy

    Science.gov (United States)

    Lahiji, Roya Roientan

    The promise of carbon nanotubes to provide high-strength composites implies that carbon nanotubes might find widespread use throughout the world, implying that humans everywhere will be exposed to carbon nanotube-containing materials. In order to study what effects if any carbon nanotubes might have on the function of living cells, we have studied the association of single stranded DNA (ssDNA) with single wall carbon nanotubes (SWCNTs) as a first step toward understanding the interaction of SWCNTs with living matter. Studies have been performed on both as-received and chemically oxidized SWCNTs to better understand the preferential association of ssDNA with SWCNTs. Samples of T30 ssDNA:SWCNT were examined under ambient conditions using non-contact Atomic Force Microscopy (AFM)) techniques. AFM images of well-dispersed, as-received SWCNTs revealed isolated features on the SWCNT that are 1.4 to 2.8 nm higher than the bare SWCNT itself. X-ray Photoemission Spectroscopy (XPS) confirmed these features to be T30 ssDNA in nature. Chemically oxidizing SWCNTs before dispersion by sonication is found to be an effective way to increase the number of T30 ssDNA features. A series of experiments showed that free radical scavengers such as ascorbic acid and trolox can effectively prevent the conjugation of ssDNA to SWCNTs, suggesting a significant role of free radicals in this association. Also hybridization of the complimentary ssDNA sequences showed the covalent nature of this association. These results are important to understanding the precise mechanism of ssDNA:SWCNT association and provide valuable information for future use in electronics, biosensors and as a possible drug carrier into individual cells. If SWCNTs are used in biosensor or circuit design applications then it is important to note how much energy can be stored in a SWCNT based on its shape and configuration before a permanent damage is introduced to it. Therefore a study has been done on bending SWCNTs into

  10. 20(R- and 20(S-Simarolide Epimers Isolated from Simaba cuneata: Chemical Shifts Assignment of Carbon and Hydrogen Atoms

    Directory of Open Access Journals (Sweden)

    Vieira Ivo José Curcino

    1999-01-01

    Full Text Available The C25-quassinoids 20(R- and 20(S-simarolide were isolated from Simaba cuneata, Simaroubaceae. The structures of these two compounds were characterized by spectral data, including 1D and 2D NMR spectra which were also used for the complete assignment of the carbon and hydrogen atom chemical shifts.

  11. Relationship between Plasma Parameters and Carbon Atom Coordination in a-C:H Films Prepared by RF Glow Discharge Decomposition

    Science.gov (United States)

    Yamamoto, Kenji; Ichikawa, Yosuke; Nakayama, Takehisa; Tawada, Yoshihisa

    1988-08-01

    Amorphous C:H films were prepared by rf glow discharge decomposition from CH4 using a permanent magnet system to apply a static magnetic field perpendicular to the rf electric field. The structure and properties of a-C:H films have been investigated systematically with respect to the hydrogen content, hardness and coordination of carbon atoms as a function of rf power (self-bias voltage). The coordination of carbon atoms has been determined by solid-state 13C magic angle spinning nuclear magnetic resonance measurements. It is found that the fraction of graphitic (sp2) versus tetrahedral (sp3) bonding increases with increasing rf power (negative self-bias voltage). Film hardness is understood in terms of the balance between the incorporated hydrogen and the fraction of graphitic (sp2) versus tetrahedral (sp3) bonding. The production of ionic and neutral species from a glow discharge has also been monitored by mass spectroscopy and optical emission spectroscopy to investigate the relation between plasma parameters and carbon atom coordination. Using these measurements and negative self-bias measurements, it is shown that the coordination of carbon atoms is determined not only by the energy of impinging ions on the substrate but also by the type of active species. In addition, the neutral and ionic C2H2 related species are thought to be some of the species which increase the fraction of graphitic (sp2) versus tetrahedral (sp3) bonding.

  12. A diastereoselective unique route to cyclopropanes functionalized at all three ring carbon atoms from acyclic vinyl sulfone-modified carbohydrates.

    Science.gov (United States)

    Atta, Ananta Kumar; Pathak, Tanmaya

    2009-04-03

    In a departure from the current trend of using metal-catalyzed routes to cyclopropanation, pentosyl and hexosyl vinyl sulfone-modified carbohydrates having the terminal double bond and a suitably positioned leaving group are reacted in a stereoselective fashion with a series of nucleophiles to yield a myriad of cyclopropanes substituted at all three ring carbon atoms.

  13. Fragmentation of neutral carbon clusters formed by high velocity atomic collision; Fragmentation d'agregats de carbone neutres formes par collision atomique a haute vitesse

    Energy Technology Data Exchange (ETDEWEB)

    Martinet, G

    2004-05-01

    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)

  14. On the vibrational behavior of single- and double-walled carbon nanotubes under the physical adsorption of biomolecules in the aqueous environment: a molecular dynamics study.

    Science.gov (United States)

    Ajori, S; Ansari, R; Darvizeh, M

    2016-03-01

    The adsorption of biomolecules on the walls of carbon nanotubes (CNTs) in an aqueous environment is of great importance in the field of nanobiotechnology. In this study, molecular dynamics (MD) simulations were performed to understand the mechanical vibrational behavior of single- and double-walled carbon nanotubes (SWCNTs and DWCNTs) under the physical adsorption of four important biomolecules (L-alanine, guanine, thymine, and uracil) in vacuum and an aqueous environment. It was observed that the natural frequencies of these CNTs in vacuum reduce under the physical adsorption of biomolecules. In the aqueous environment, the natural frequency of each pure CNT decreased as compared to its natural frequency in vacuum. It was also found that the frequency shift for functionalized CNTs as compared to pure CNTs in the aqueous environment was dependent on the radius and the number of walls of the CNT, and could be positive or negative.

  15. International Atomic Energy Agency (IAEA) Coordinated Research Projects on Structural Integrity of Reactor Pressure Vessels

    Energy Technology Data Exchange (ETDEWEB)

    Server, W. L. [ATI Consulting, Pinehurst, NC; Nanstad, Randy K [ORNL

    2009-01-01

    The International Atomic Energy Agency (IAEA) has conducted a series of Coordinated Research Projects (CRPs) that have focused on irradiated reactor pressure vessel (RPV) steel fracture toughness properties and approaches for assuring structural integrity of RPVs throughout operating life. A series of nine CRPs have been sponsored by the IAEA, starting in the early 1970s, focused on neutron radiation effects on RPV steels. The purpose of the CRPs was to develop comparisons and correlations to test the uniformity of irradiated results through coordinated international research studies and data sharing. Consideration of dose rate effects, effects of alloying (nickel, manganese, silicon, etc.) and residual elements (eg., copper and phosphorus), and drop in upper shelf toughness are also important for assessing neutron embrittlement effects. The ultimate use of embrittlement understanding is assuring structural integrity of the RPV under current and future operation and accident conditions. Material fracture toughness is the key ingredient needed for this assessment, and many of the CRPs have focused on measurement and application of irradiated fracture toughness. This paper presents an overview of the progress made since the inception of the CRPs in the early 1970s. The chronology and importance of each CRP have been reviewed and put into context for continued and long-term safe operation of RPVs.

  16. PREFACE: International Conference on Many Particle Spectroscopy of Atoms, Molecules, Clusters and Surfaces

    Science.gov (United States)

    Dowek, Danielle; Bennani, Azzedine; Lablanquie, Pascal; Maquet, Alfred

    2008-12-01

    The 2008 edition of the International Conference on Many Particle Spectroscopy of Atoms, Molecules, Clusters and Surfaces was held in Paris from 30 June to 2 July 2008. This biennial conference alternates with the International Symposium on (e,2e), Double Photoionization and Related Topics which is a satellite of the International Conference on Photonic, Electronic and Atomic Collisions (ICPEAC) conference. Over 110 participants from 20 countries gathered to examine the latest developments in the field of radiation interactions with matter. These include electron-electron correlation effects in excitation and in single and multiple ionization of atoms, molecules, clusters and surfaces with various projectiles: electrons, photons and ions. The present proceedings gathers the contributions of invited speakers and is intended to provide a detailed state-of-the-art account of the various facets of the field. Special thanks are due to Université Paris Sud XI, CNRS, and the laboratories LCAM, LIXAM and LCPMR which provided financial support for the organization of the conference. We are also grateful to the contribution of the companies Varian and RoentDek Handels GmbH. Guest Editors: Danielle Dowek and Azzedine Bennani LCAM, Université Paris Sud XI, France Pascal Lablanquie and Alfred Maquet LCPMR, Université Pierre et Marie Curie, Paris, France INTERNATIONAL SCIENTIFIC COMMITTEE Lorenzo Avaldi, (Italy) Alexei Grum Grzhimailo, (Russia) Klaus Bartschat, (USA) Nikolai Kabachnik, (Russia) Jamal Berakdar, (Germany) Birgit Lohmann, (Australia) Nora Berrah, (USA) Don H Madison, (USA) Michael Brunger, (Australia) Francis Penent, (France) Albert Crowe, (UK) Bernard Piraux, (Belgium) Claude Dal Cappello, (France) Roberto Rivarola, (Argentina) JingKang Deng, (China) Emma Sokkel, (Ireland) Alexander Dorn, (Germany) Giovanni Stefani, (Italy) Reinhardt Dorner, (Germany) Noboru Watanabe, (Japan) François Frémont, (France) LOCAL ORGANIZING COMMITTEE Azzedine BENNANI (Chair

  17. 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.

  18. Removal of endocrine disrupting chemicals from aqueous phase using spherical microporous carbon prepared from waste polymeric exchanger.

    Science.gov (United States)

    Long, Chao; Lu, Jundong; Li, Aimin; Zhang, Quanxing

    2009-01-01

    A spherical microporous carbon adsorbent (CR-1), which was developed by carbonization and activation of the waste polysulfonated cation-exchanger, was used to remove Dimethyl phthalate (DMP) and 2, 4-dichlorophenol (2, 4-DCP) as the model compounds of EDCs from the aqueous solution. Four adsorption isotherm models, Langmuir, Freundlich, Toth and Polanyi-Dubinin-Manes equations were tested to correlate the experimental data, Toth and Polanyi-Dubinin-Manes isotherms models provided the best correlation. The Henry's law constants calculated from Toth equation were found to be 705.957 and 6,724.713 L g(-1) for 2, 4-DCP and DMP at 298 K, respectively, and the larger exponents n of the Freundlich model were 9.011 and 9.93 for 2, 4-DCP and DMP at 298 K, respectively. The values of Henry's law constants and exponent n of the Freundlich suggested that CR-1 was an effective adsorbent for removal of low concentrations of DMP and 2, 4-DCP from aqueous solution. Moreover, the adsorption kinetics results showed that adsorption of 2, 4-DCP and DMP on CR-1 was a pseudo-second-order process controlled by intra-particle diffusion and that adsorption uptake reached quickly half of equilibrium capacities within 20 min.

  19. Effective dispersion of multi-walled carbon nanotubes in aqueous solution using an ionic-gemini dispersant.

    Science.gov (United States)

    Hou, Jiangtao; Du, Wenbo; Meng, Fanjing; Zhao, Chenchen; Du, Xian

    2018-02-15

    A promising ionic-gemini molecule, 4, 4'-di (n-tetradecyl) diphenylmethane disulfate salt (DSDM), is reported for effective dispersion of multi-walled carbon nanotubes (MWCNTs) in aqueous medium in the present investigation. The dispersibility and stability of the DSDM-modified MWCNTs were characterized by UV-vis spectrophotometer, Raman spectroscopy, Fourier transform infrared spectroscopy, transmission electron microscopy and zeta potential measurements. The hydrophobic interaction between alky chains and carbon nanotubes as well as the π-π-stacking interaction between benzene rings and carboatomic rings in MWCNTs enables a successful modification of DSDM onto the MWCNT surface. The dispersed MWCNTs individually existed in dispersion with no structural damage, indicating a much better performance than the MWCNTs dispersed by the sodium dodecylbenzene sulfonate (SDBS), a frequently reported single-chain ionic dispersant. Surface potential measurements showed that the DSDM-modified MWCNTs were negatively charged, giving rise to electrostatic repulsion between the MWCNTs in aqueous solution. A better MWCNT dispersion effect was observed with the increase in MWCNT surface potential, and the dispersion with high MWCNT surface potential presents high dispersion stability with no agglomeration appeared for more than 5 months. The magnesium (Mg) matrix composite fabricated based on the DSDM-dispersed MWCNTs demonstrated excellent mechanical properties compared to pure Mg. Our research may provide an alternative way to improve the mechanical properties of composites. Copyright © 2017 Elsevier Inc. All rights reserved.

  20. Medical physics in Europe following recommendations of the International Atomic Energy Agency

    Science.gov (United States)

    Lopes, Maria do Carmo; Drljević, Advan; Gershkevitsh, Eduard; Pesznyak, Csilla

    2016-01-01

    Background Medical physics is a health profession where principles of applied physics are mostly directed towards the application of ionizing radiation in medicine. The key role of the medical physics expert in safe and effective use of ionizing radiation in medicine was widely recognized in recent European reference documents like the European Union Council Directive 2013/59/EURATOM (2014), and European Commission Radiation Protection No. 174, European Guidelines on Medical Physics Expert (2014). Also the International Atomic Energy Agency (IAEA) has been outspoken in supporting and fostering the status of medical physics in radiation medicine through multiple initiatives as technical and cooperation projects and important documents like IAEA Human Health Series No. 25, Roles and Responsibilities, and Education and Training Requirements for Clinically Qualified Medical Physicists (2013) and the International Basic Safety Standards, General Safety Requirements Part 3 (2014). The significance of these documents and the recognition of the present insufficient fulfilment of the requirements and recommendations in many European countries have led the IAEA to organize in 2015 the Regional Meeting on Medical Physics in Europe, where major issues in medical physics in Europe were discussed. Most important outcomes of the meeting were the recommendations addressed to European member states and the survey on medical physics status in Europe conducted by the IAEA and European Federation of Organizations for Medical Physics. Conclusions Published recommendations of IAEA Regional Meeting on Medical Physics in Europe shall be followed and enforced in all European states. Appropriate qualification framework including education, clinical specialization, certification and registration of medical physicists shall be established and international recommendation regarding staffing levels in the field of medical physics shall be fulfilled in particular. European states have clear

  1. Medical physics in Europe following recommendations of the International Atomic Energy Agency.

    Science.gov (United States)

    Casar, Bozidar; Lopes, Maria do Carmo; Drljević, Advan; Gershkevitsh, Eduard; Pesznyak, Csilla

    2016-03-01

    Medical physics is a health profession where principles of applied physics are mostly directed towards the application of ionizing radiation in medicine. The key role of the medical physics expert in safe and effective use of ionizing radiation in medicine was widely recognized in recent European reference documents like the European Union Council Directive 2013/59/EURATOM (2014), and European Commission Radiation Protection No. 174, European Guidelines on Medical Physics Expert (2014). Also the International Atomic Energy Agency (IAEA) has been outspoken in supporting and fostering the status of medical physics in radiation medicine through multiple initiatives as technical and cooperation projects and important documents like IAEA Human Health Series No. 25, Roles and Responsibilities, and Education and Training Requirements for Clinically Qualified Medical Physicists (2013) and the International Basic Safety Standards, General Safety Requirements Part 3 (2014). The significance of these documents and the recognition of the present insufficient fulfilment of the requirements and recommendations in many European countries have led the IAEA to organize in 2015 the Regional Meeting on Medical Physics in Europe, where major issues in medical physics in Europe were discussed. Most important outcomes of the meeting were the recommendations addressed to European member states and the survey on medical physics status in Europe conducted by the IAEA and European Federation of Organizations for Medical Physics. Published recommendations of IAEA Regional Meeting on Medical Physics in Europe shall be followed and enforced in all European states. Appropriate qualification framework including education, clinical specialization, certification and registration of medical physicists shall be established and international recommendation regarding staffing levels in the field of medical physics shall be fulfilled in particular. European states have clear legal and moral

  2. Solar-Driven Reduction of Aqueous Protons Coupled to Selective Alcohol Oxidation with a Carbon Nitride-Molecular Ni Catalyst System.

    Science.gov (United States)

    Kasap, Hatice; Caputo, Christine A; Martindale, Benjamin C M; Godin, Robert; Lau, Vincent Wing-Hei; Lotsch, Bettina V; Durrant, James R; Reisner, Erwin

    2016-07-27

    Solar water-splitting represents an important strategy toward production of the storable and renewable fuel hydrogen. The water oxidation half-reaction typically proceeds with poor efficiency and produces the unprofitable and often damaging product, O2. Herein, we demonstrate an alternative approach and couple solar H2 generation with value-added organic substrate oxidation. Solar irradiation of a cyanamide surface-functionalized melon-type carbon nitride ((NCN)CNx) and a molecular nickel(II) bis(diphosphine) H2-evolution catalyst (NiP) enabled the production of H2 with concomitant selective oxidation of benzylic alcohols to aldehydes in high yield under purely aqueous conditions, at room temperature and ambient pressure. This one-pot system maintained its activity over 24 h, generating products in 1:1 stoichiometry, separated in the gas and solution phases. The (NCN)CNx-NiP system showed an activity of 763 μmol (g CNx)(-1) h(-1) toward H2 and aldehyde production, a Ni-based turnover frequency of 76 h(-1), and an external quantum efficiency of 15% (λ = 360 ± 10 nm). This precious metal-free and nontoxic photocatalytic system displays better performance than an analogous system containing platinum instead of NiP. Transient absorption spectroscopy revealed that the photoactivity of (NCN)CNx is due to efficient substrate oxidation of the material, which outweighs possible charge recombination compared to the nonfunctionalized melon-type carbon nitride. Photoexcited (NCN)CNx in the presence of an organic substrate can accumulate ultralong-lived "trapped electrons", which allow for fuel generation in the dark. The artificial photosynthetic system thereby catalyzes a closed redox cycle showing 100% atom economy and generates two value-added products, a solar chemical, and solar fuel.

  3. Adsorption of As(V), Cd(II) and Pb(II), in Multicomponent Aqueous Systems using Activated Carbons.

    Science.gov (United States)

    Pirilä, M; Cruz, G J F; Ainassaari, K; Gomez, M M; Matějová, L; Keiski, R L

    2017-09-01

      This paper studies the use of two activated carbon samples made of cocoa pod husk (CPH-AC) and one commercial activated carbon sample in the adsorption of As(V), Cd(II) and Pb(II) from multicomponent synthetic solutions and from the Puyango-Tumbes River water, a river located in northwest Peru. The characterization of the activated carbon samples was conducted. The CPH-AC samples exhibited a specific surface area (SBET) between 709 and 1117 m2/g and a pH point of zero charge (pHPZC) between 4.4 ± 0.2 and 5 ± 0.2, while the commercial material gave an SBET value of 775 m2/g and a pHPZC value of 7.6 ± 0.1. All the evaluated samples displayed the capacity to adsorb As(V), Cd(II) and Pb(II) from both aqueous systems. The adsorption efficiency for Pb was outstanding reaching the value of 89%. A pseudo-second order kinetic model was satisfactorily applied for most of the activated carbon samples.

  4. Adsorption of U(VI) ions from aqueous solutions by activated carbon prepared from Antep pistachio (Pistacia vera L.) shells

    Energy Technology Data Exchange (ETDEWEB)

    Donat, Ramazan [Pamukkale Univ., Denizli (Turkey). Dept. of Chemistry; Erden, Kadriye Esen [Pamukkale Univ., Kinikli-Denizli (Turkey). Denizli Vocational School of Technical Sciences

    2017-08-01

    Antep pistachio (Pistacia vera L.) shells an abundant and low cost natural resource in Turkey was used to prepare activated carbon by physiochemical activation and carbon dioxide (CO{sub 2}) atmosphere as the activating agents at 700 C for 2 h. The adsorption equilibrium of U(VI) from aqueous solutions on such carbon has been studied using a batch system. The parameters that affect the U(VI) adsorption, such as particle size of adsorbent, contact time, of pH of the solution, and temperature, have been investigated and conditions have also been optimized. The equilibrium data for U(VI) ions' adsorption onto activated carbon well fitted to the Langmuir equation, with a maximum monolayer adsorption capacity of 8.68 mg/g, The Freundlich and Dubinin-Radushkevich (D-R) isotherms have been applied and the data correlated well with Freundlich model and that the adsorption is physical in nature (E{sub a}=15.46 kJ/mol). Thermodynamic parameters [ΔH{sub s}=11.33 kJ/mol, ΔS=0.084 kJ/molK, ΔG (293.15 K)=-13.29 kJ/mol] showed the endothermic heat of adsorption and the feasibility of the process.

  5. Hexavalent chromium removal from aqueous solution by algal bloom residue derived activated carbon: Equilibrium and kinetic studies

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Hong; Tang Yi; Cai Dongqing; Liu Xianan; Wang Xiangqin [Key Laboratory of Ion Beam Bioengineering, Institute of Plasma Physics, Chinese Academy of Sciences, Hefei, Anhui 230031 (China); Huang Qing, E-mail: huangq@ipp.ac.cn [Key Laboratory of Ion Beam Bioengineering, Institute of Plasma Physics, Chinese Academy of Sciences, Hefei, Anhui 230031 (China); Yu Zengliang, E-mail: zlyu@ipp.ac.cn [Key Laboratory of Ion Beam Bioengineering, Institute of Plasma Physics, Chinese Academy of Sciences, Hefei, Anhui 230031 (China)

    2010-09-15

    A novel approach to prepare activated carbon from blue-green algal bloom residue has been tried for first time and its adsorption capability to remove hexavalent chromium Cr(VI) from aqueous solution has been examined. For this algal bloom residue derived activated carbon, the physical characters regarding adsorption capability were analyzed by scanning electron microscope (SEM), energy dispersive X-ray spectroscope (EDS) and Fourier transform infrared (FTIR) spectroscopy. Batch studies showed that initial pH, absorbent dosage, and initial concentration of Cr(VI) were important parameters for Cr(VI) absorption. It was found that initial pH of 1.0 was most favorable for Cr(VI) removal. The adsorption process followed the pseudo-second-order equation and Freundlich isotherm. The maximum adsorption capacity for Cr(VI) was 155.52 mg g{sup -1} in an acidic medium, which is comparable to best result from activated carbons derived from biomass. Therefore, this work put forward a nearly perfect solution which on one hand gets rid of environment-unfriendly algae residue while on the other hand produces high-quality activated carbon that is in return advantageous to environment protection.

  6. Hexavalent chromium removal from aqueous solution by algal bloom residue derived activated carbon: equilibrium and kinetic studies.

    Science.gov (United States)

    Zhang, Hong; Tang, Yi; Cai, Dongqing; Liu, Xianan; Wang, Xiangqin; Huang, Qing; Yu, Zengliang

    2010-09-15

    A novel approach to prepare activated carbon from blue-green algal bloom residue has been tried for first time and its adsorption capability to remove hexavalent chromium Cr(VI) from aqueous solution has been examined. For this algal bloom residue derived activated carbon, the physical characters regarding adsorption capability were analyzed by scanning electron microscope (SEM), energy dispersive X-ray spectroscope (EDS) and Fourier transform infrared (FTIR) spectroscopy. Batch studies showed that initial pH, absorbent dosage, and initial concentration of Cr(VI) were important parameters for Cr(VI) absorption. It was found that initial pH of 1.0 was most favorable for Cr(VI) removal. The adsorption process followed the pseudo-second-order equation and Freundlich isotherm. The maximum adsorption capacity for Cr(VI) was 155.52 mg g(-1) in an acidic medium, which is comparable to best result from activated carbons derived from biomass. Therefore, this work put forward a nearly perfect solution which on one hand gets rid of environment-unfriendly algae residue while on the other hand produces high-quality activated carbon that is in return advantageous to environment protection. Copyright 2010 Elsevier B.V. All rights reserved.

  7. 2nd International Symposium "Atomic Cluster Collisions : Structure and Dynamics from the Nuclear to the Biological Scale"

    CERN Document Server

    Solov'yov, Andrey; ISACC 2007; Latest advances in atomic cluster collisions

    2008-01-01

    This book presents a 'snapshot' of the most recent and significant advances in the field of cluster physics. It is a comprehensive review based on contributions by the participants of the 2nd International Symposium on Atomic Cluster Collisions (ISACC 2007) held in July 19-23, 2007 at GSI, Darmstadt, Germany. The purpose of the Symposium is to promote the growth and exchange of scientific information on the structure and properties of nuclear, atomic, molecular, biological and complex cluster systems studied by means of photonic, electronic, heavy particle and atomic collisions. Particular attention is devoted to dynamic phenomena, many-body effects taking place in cluster systems of a different nature - these include problems of fusion and fission, fragmentation, collective electron excitations, phase transitions, etc.Both the experimental and theoretical aspects of cluster physics, uniquely placed between nuclear physics on the one hand and atomic, molecular and solid state physics on the other, are discuss...

  8. Adsorption of low concentration ceftazidime from aqueous solutions using impregnated activated carbon promoted by Iron, Copper and Aluminum

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Xiang, E-mail: huxiang@mail.buct.edu.cn [College of Chemical Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Research Centre for Environmental Pollution Control and Resource Reuse Engineering of Beijing City, Beijing 100029 (China); Zhang, Hua [College of Chemical Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Research Centre for Environmental Pollution Control and Resource Reuse Engineering of Beijing City, Beijing 100029 (China); Sun, Zhirong, E-mail: zrsun@bjut.edu.cn [College of Environmental & Energy Engineering, Beijing University of Technology, Beijing 100124 (China)

    2017-01-15

    Graphical abstract: The graphic abstract describes the research that we used modified activated carbons impregnated with iron nitrate, copper nitrate and aluminium nitrate to adsorb ceftazidime from aqueous solution. The surface functional groups of the modified activated carbons were different, and thus resulted in the big difference in the adsorption performance of the modified activated carbons. The theory and the experiments both showed the preferable adsorption of ceftazidime could be achieved on modified activated carbons. - Highlights: • Three modified activated carbons were prepared by impregnating metal nitrate. • Characteristics of the modified activated carbons were analyzed. • Adsorption capacity of ceftazidime on modified activated carbons was improved. • The adsorption behavior of ceftazidime on modified activated carbons were revealed. • The nature of ceftazidime adsorption on modified activated carbons was elucidated. - Abstract: In this paper, three impregnated activated carbon IAC (AC-Cu, AC-Fe, and AC-Al) promoted by Iron, Copper and Aluminum were used for adsorption of ceftazidime. Iron(III), Copper(II) and Aluminum(III) nitrate were used as an impregnant. The IACs were characterized by scanning electron microscope (SEM), Brunauer-Emmett-Teller (BET) surface area analyzer, Fourier transform infrared spectroscopy (FTIR) and X-ray Photoelectron Spectroscopy (XPS).The influence of factors, such as ion strength, pH, temperature, initial concentration, and concentration of natural organic matter organic matter on the adsorption process were studied. The adsorption kinetics and isotherms of ceftazidime were studied for the three IACs. The results showed that the adsorption was accurately represented by pseudo-second order model. Under different temperature, the maximum adsorption quantity of ceftazidime on AC-Cu calculated by pseudo-second order kinetic model were 200.0 mg g{sup −1} (298 K), 196.1 mg g{sup −1} (303 K) and 185.2 mg g

  9. Removal of PFOA and PFOS from aqueous solutions using activated carbon produced from Vitis vinifera leaf litter.

    Science.gov (United States)

    Fagbayigbo, Bamidele Oladapo; Opeolu, Beatrice Olutoyin; Fatoki, Olalekan Siyanbola; Akenga, Terresa Ayuko; Olatunji, Olatunde Stephen

    2017-05-01

    The removal of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) from aqueous solutions using agro-waste biomass of Vitis vinifera (grape) leaf litter was studied. Activated carbons were produced from the biomass and chemical activation achieved by using phosphoric acid (H 3 PO 4 ) and potassium hydroxide (KOH) for the modification of the carbons' surface morphology. Activated carbons were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy and Brunauer-Emmett-Teller (BET) in order to understand removal mechanisms of the contaminants by activated carbons. The effect of solution concentration, pH, adsorbent dosage, contact time and temperature was evaluated to optimize the removal efficiency of activated carbons. Adsorption isotherm models were used to analyse the equilibrium data obtained, and kinetic models were applied to study sorption mechanisms. The results fitted well into Freundlich isotherm with both AC-KOH and AC-H 3 PO 4 having high K f values. Maximum adsorption capacities for AC-H 3 PO 4 were 78.90 and 75.13 mg/g for PFOA and PFOS, respectively. Equilibrium was reached before 60 min on both adsorbents, and thermodynamic studies indicated that the process was exothermic and spontaneous. Surface morphology showed the abundance of microspores (>60%) with BET total surface area of 295.488 and 158.67 m 2 /g for AC-H 3 PO 4 and AC-KOH activated carbons, respectively. Removal efficiencies were 95 and 90% for PFOA using AC-H 3 PO 4 and AC-KOH, respectively; corresponding values for PFOS were 94 and 88%. Adsorbents' removal capacities depended on the physicochemical characteristics of adsorbents.

  10. Preparation and Utilization of Corncob Activated Carbon for Dyes Removal from Aqueous Solutions: Batch and Continuous Study

    Directory of Open Access Journals (Sweden)

    Mohammad Abd Muslim AL- Tufaily

    2016-09-01

    Full Text Available Commercial activated carbon and produced corncob activated carbon were used for the adsorption of methylene blue dye from aqueous solution using batch and continuous processes. Batch processes were conducted to study the effects of solution pH, contact time, adsorbent dose, agitation speed and initial dye concentration. The optimum values for methylene blue dye adsorption were: solution pHs of 6 and 7, contact times of 8 and 5 hr., adsorbent dosages of 1.5, and 0.5 gm, agitation speeds of 200 and 250 rpm and initial dye concentration of 50 mg/l calculated by commercial activated carbon and corncob activated carbon respectively. Two isotherm models, Freundlich and Langmuir fitted with the experimental data found from batch processes, the Langmuir model fitted well than the Freundlich, with maximum adsorption capacities of 16.21 and 30.95 mg/g and R2 of 0.952 and 0.992 predicted by commercial activated carbon and corncob activated carbon respectively. Radial and vertical flow regime reactors were conducted in column tests for the two adsorbent materials at different three flow rates (0.2, 0.3 and 0.4 L/min and initial dye concentrations 15 mg/l, the same volume of (775 ml from adsorbent materials used for both radial and vertical reactors to make a comparison between the capacity of the adsorbent materials each with another and between the performance of radial and vertical flow regime reactors configurations on breakthrough curves behavior. Radial flow regime reactor showed good results in comparison with vertical flow regime reactor.

  11. Nitrogen-Doped Porous Carbons from Ionic Liquids@MOF: Remarkable Adsorbents for Both Aqueous and Nonaqueous Media.

    Science.gov (United States)

    Ahmed, Imteaz; Panja, Tandra; Khan, Nazmul Abedin; Sarker, Mithun; Yu, Jong-Sung; Jhung, Sung Hwa

    2017-03-22

    Porous carbons were prepared from a metal-organic framework (MOF, named ZIF-8), with or without modification, via high-temperature pyrolysis. Porous carbons with high nitrogen content were obtained from the calcination of MOF after introducing an ionic liquid (IL) (IL@MOF) via the ship-in-bottle method. The MOF-derived carbons (MDCs) and IL@MOF-derived carbons (IMDCs) were characterized using various techniques and used for liquid-phase adsorptions in both water and hydrocarbon to understand the possible applications in purification of water and fuel, respectively. Adsorptive performances for the removal of organic contaminants, atrazine (ATZ), diuron, and diclofenac, were remarkably enhanced with the modification/conversion of MOFs to MDC and IMDC. For example, in the case of ATZ adsorption, the maximum adsorption capacity of IMDC (Q 0 = 208 m 2 /g) was much higher than that of activated carbon (AC, Q 0 = 60 m 2 /g) and MDC (Q 0 = 168 m 2 /g) and was found to be the highest among the reported results so far. The results of adsorptive denitrogenation and desulfurization of fuel were similar to that of water purification. The IMDCs are very useful in the adsorptions since these new carbons showed remarkable performances in both the aqueous and nonaqueous phases. These results are very meaningful because hydrophobic and hydrophilic adsorbents are usually required for the adsorptions in the water and fuel phases, respectively. Moreover, a plausible mechanism, H-bonding, was also suggested to explain the remarkable performance of the IMDCs in the adsorptions. Therefore, the IMDCs derived from IL@MOF might have various applications, especially in adsorptions, based on high porosity, mesoporosity, doped nitrogen, and functional groups.

  12. Non-aqueous formation of the calcium carbonate polymorph vaterite: astrophysical implications

    OpenAIRE

    Day, Sarah J.; Thompson, Stephen P.; 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 cal...

  13. Metal Oxide-Carbon Nanocomposites for Aqueous and Nonaqueous Supercapacitors Project

    Data.gov (United States)

    National Aeronautics and Space Administration — This Small Business Innovation Research Phase I effort focuses on development of novel metal-oxide-carbon nanocomposites for application in pseudocapacitive...

  14. Atomic-scale scanning tunneling microscopy study of plasma-oxidized ultrahigh-modulus carbon fiber surfaces.

    Science.gov (United States)

    Paredes, J I; Martínez-Alonso, A; Tascón, J M D

    2003-02-15

    In the present work, scanning tunneling microscopy (STM) was employed to study the surface modification of ultrahigh modulus carbon fibers at the atomic level by oxygen plasma. As detected by STM, the distinctive feature of the fresh, untreated surface was the general presence of atomic-scale arrangements in different degrees of order (from atomic-sized spots without a clearly ordered disposition to triangular patterns identical to those typical of perfect graphite). Following fiber exposure to the plasma, the STM images showed evidence of the abstraction of carbon atoms from random locations on the fiber surface, giving rise to the development of defects (i.e., structural disorder), which in turn were the places where oxygen could be introduced during and after the plasma etching. It was observed that the most effective treatments in terms of extent of surface structural modification (disordering) and uniform introduction of oxygen were those carried out for just a few ( approximately 3) minutes. Considerably shorter exposures failed to provide a homogeneous modification and many locations on the fiber surface remained unaltered, retaining their original atomic-scale order, whereas longer treatments did not bring about further structural changes to the surface and only led to fiber consumption. These results are consistent with previous X-ray photoelectron spectroscopy measurements on these fibers and provide an atomic-level understanding of the saturation effect observed in the surface oxygen concentration of this and other types of carbon fibers with plasma oxidation. Such understanding may also prove helpful for the accurate control and optimization of fiber-matrix interaction in composite materials.

  15. Effect of Fe ion concentration on fatigue life of carbon steel in aqueous CO2 environment

    DEFF Research Database (Denmark)

    Rogowska, Magdalena; Gudme, J.; Rubin, A.

    2016-01-01

    In this work, the corrosion fatigue behaviour of steel armours used in the flexible pipes, in aqueous solutions initially containing different concentrations of Fe2+, was investigated by four-point bending testing under saturated 1 bar CO2 condition. Corrosion fatigue results were supported with ......, fatigue samples experienced the same corrosion rate as samples that were not subjected to dynamic loading.......In this work, the corrosion fatigue behaviour of steel armours used in the flexible pipes, in aqueous solutions initially containing different concentrations of Fe2+, was investigated by four-point bending testing under saturated 1 bar CO2 condition. Corrosion fatigue results were supported with ex...... situ measurements of Fe2+ and pH. Characterisation of the corrosion scales and crack formations was performed using microscopic and diffraction techniques. Fatigue results showed two times better fatigue life, at the stress ranges of 250 MPa, for samples tested in solutions containing the concentration...

  16. US scientific contributions to the water resources program of the International Atomic Energy Agency

    Science.gov (United States)

    Aggarwal, P. K.; Schneider, V. R.

    2007-12-01

    It is well recognized that a better understanding of the water cycle and increased availability of hydrological information for surface and groundwater resources are key factors in the ability to sustainably manage water resources. Since its inception in 1957, the International Atomic Energy Agency (IAEA) has played a critical role in developing isotope applications for hydrology and building scientific capacity in developing countries. Through an active technical cooperation program with a funding of nearly $8M per biennium, the IAEA assists developing countries in using isotope techniques for the assessment and monitoring of water resources, in particular, groundwater resources. In addition, substantial human resources and institutional capacity are built through the provision of training and appropriate equipment for monitoring. The water resources program of the IAEA is implemented with the support of a number of experts and the United States contributes extensively to this program. Although spanning the entire 50 year history of the IAEA, the contribution of US scientists, and particularly those from the US Geological Survey, has been substantial over the past 10 years. These contributions have included assistance in technical cooperation projects in Africa, Latin America and Asia, as well as internationally coordinated research projects in vadose zone hydrology, surface water - groundwater interactions, and regional aquifer studies. In Ethiopia, a national groundwater assessment program was formulated and a computer database was provided to manage hydrological information. A robust program of capacity building in cooperation with the USGS and Argonne National Laboratory has provided training to a number of IAEA-sponsored candidates from Africa and Latin America. This paper will describe the objectives and results of some of these cooperative efforts.

  17. PRECONCENTRATION OF COPPER FROM SYNTHETIC AQUEOUS SOLUTIONS USING MULTIWALLED CARBON NANOTUBES

    OpenAIRE

    Semančíková, Jana; Remeteiová, Dagmar

    2016-01-01

    The determination of heavy metal contents in various components of the environment is very important in the context of environmental protection. In laboratory practice often happens that the determination of trace and ultra-trace contents of heavy metals in natural aqueous samples by available method is not sufficient with respect of required accuracy. In such cases it is necessary to include appropriate treatment of the samples prior to their analysis. For the purpose of preconcentration of ...

  18. The international atomic energy agency's programme on utilization of accelerators

    Energy Technology Data Exchange (ETDEWEB)

    Dytlewski, Nikolai [International Atomic Energy Agency, Wagramer Str. 5, A-1400 Vienna (Austria); Mank, Guenter [International Atomic Energy Agency, Wagramer Str. 5, A-1400 Vienna (Austria)]. E-mail: g.mank@iaea.org; Rosengard, Ulf [International Atomic Energy Agency, Wagramer Str. 5, A-1400 Vienna (Austria); Bamford, Samuel [International Atomic Energy Agency, Wagramer Str. 5, A-1400 Vienna (Austria); Markowicz, Andrzej [International Atomic Energy Agency, Wagramer Str. 5, A-1400 Vienna (Austria); Wegrzynek, Dariusz [International Atomic Energy Agency, Wagramer Str. 5, A-1400 Vienna (Austria)

    2006-06-23

    Low-energy accelerators have in the past produced a major part of our current knowledge of nuclear physics. Today they are mainly used for applied research and industrial applications. In view of this, the International Atomic Energy Agency (IAEA) has during recent years initiated several Coordinated Research Projects (CRPs) concerning Ion Beam Analysis of Materials, Accelerator Mass Spectrometry and Nuclear Microprobe Techniques. The CRPs involve laboratories from developing as well as developed Member States, networking on a common topic coordinated by the IAEA. In order to facilitate networking, the IAEA has recently published the 'World Survey of Accelerator Based Analytical Techniques' available on the Internet and as a CD-ROM. The IAEA maintains also a beamline at a 6 MV Van de Graaff accelerator in the Rudjer Boskovic Institute, Zagreb, Croatia. Small and medium power accelerator driven spallation neutron sources will become more important as many small neutron producing research reactors are approaching the end of their useful working life. The IAEA has, within its Department for Nuclear Sciences and Applications, a programme on the Effective Utilization of Accelerators. This programme helps Member States, in particular developing Member States, in finding new areas of applications for their low and medium energy accelerators through increased participation in activities such as Coordinated Research Projects, Technical Meetings and Conferences. This paper describes the IAEA's current programme on accelerator utilization and proposed future activities.

  19. Justification of diagnostic medical exposures: some practical issues. Report of an International Atomic Energy Agency Consultation

    Science.gov (United States)

    Malone, J; Guleria, R; Craven, C; Horton, P; Järvinen, H; Mayo, J; O’reilly, G; Picano, E; Remedios, D; Le Heron, J; Rehani, M; Holmberg, O; Czarwinski, R

    2012-01-01

    Objectives The Radiation Protection of Patients Unit of the International Atomic Energy Agency (IAEA) is concerned about the effectiveness of justification of diagnostic medical exposures. Recent published work and the report of an initial IAEA consultation in the area gave grounds for such concerns. There is a significant level of inappropriate usage, and, in some cases, a poor level of awareness of dose and risk among some key groups involved. This article aims to address this. Methods The IAEA convened a second group of experts in November 2008 to review practical and achievable actions that might lead to more effective justification. Results This report summarises the matters that this group considered and the outcome of their deliberations. There is a need for improved communication, both within professions and between professionals on one hand, and between professionals and the patients/public on the other. Coupled with this, the issue of consent to imaging procedures was revisited. The need for good evidence-based referral guidelines or criteria of acceptability was emphasised, as was the need for their global adaptation and dissemination. Conclusion Clinical audit was regarded as a key tool in ensuring that justification becomes an effective, transparent and accountable part of normal radiological practice. In summary, justification would be facilitated by the “3 As”: awareness, appropriateness and audit. PMID:21343316

  20. Bibliography of electron and photon cross sections with atoms and molecules published in the 20th century. Carbon dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Hayashi, Makoto [Gaseous Electronics Institute, Nagoya, Aichi (Japan)

    2003-04-01

    A bibliography of original and review reports of experiments or theories of electron and photon cross sections and also electron swarm data are presented for atomic or molecular species with specified targets. These works covered 17 atoms and 51 molecules. The present bibliography is only for carbon dioxide (CO{sub 2}). About 1,240 papers were compiled. A comprehensive author index is included. The bibliography covers the period 1901 through 2000 for CO{sub 2}. Finally, author's comments for CO{sub 2} electron collision cross sections are given. (author)

  1. Sub-5 nm nanostructures fabricated by atomic layer deposition using a carbon nanotube template

    Science.gov (United States)

    Woo, Ju Yeon; Han, Hyo; Kim, Ji Weon; Lee, Seung-Mo; Ha, Jeong Sook; Shim, Joon Hyung; Han, Chang-Soo

    2016-07-01

    The fabrication of nanostructures having diameters of sub-5 nm is very a important issue for bottom-up nanofabrication of nanoscale devices. In this work, we report a highly controllable method to create sub-5 nm nano-trenches and nanowires by combining area-selective atomic layer deposition (ALD) with single-walled carbon nanotubes (SWNTs) as templates. Alumina nano-trenches having a depth of 2.6 ∼ 3.0 nm and SiO2 nano-trenches having a depth of 1.9 ∼ 2.2 nm fully guided by the SWNTs have been formed on SiO2/Si substrate. Through infilling ZnO material by ALD in alumina nano-trenches, well-defined ZnO nanowires having a thickness of 3.1 ∼ 3.3 nm have been fabricated. In order to improve the electrical properties of ZnO nanowires, as-fabricated ZnO nanowires by ALD were annealed at 350 °C in air for 60 min. As a result, we successfully demonstrated that as-synthesized ZnO nanowire using a specific template can be made for various high-density resistive components in the nanoelectronics industry.

  2. Atomic-force-microscopy nanowriting on ultrathin tetrahedral amorphous carbon films

    Science.gov (United States)

    Pivovarov, Pavel A.; Zavedeev, Evgeny V.; Frolov, Vadim D.; Roch, Teja; Scheibe, Hans-Joachim; Pimenov, Sergei M.

    2016-11-01

    We report the atomic-force-microscopy (AFM)-based nanolithography writing of surface patterns on ultrathin (nanoletters') is demonstrated, depending on the magnitude and duration of the voltage pulses applied between the ta-C film and conductive probe, and the relative humidity of ambient air. It is found that the AFM tip-assisted nanowriting process occurring under (1) the presence of adsorbed water layers on the ta-C surface, (2) the applied voltage of >4 V, and (3) the contact pressures in the GPa range results in the formation of a novel carbon phase in a nm-thick surface layer characterized by the lower density, lower mechanical strength, lower electrical conductivity, and increased nanofriction as compared to the original film. The structure of the tip-modified nm-thick layer on the ta-C film is assumed to be a structure of graphite oxide which can be further modified in the presence of water under high contact pressures.

  3. Mechanism and model of atomic hydrogen cleaning for different types of carbon contamination on extreme ultraviolet multilayers

    Energy Technology Data Exchange (ETDEWEB)

    Song, Yuan [State Key Laboratory of Applied Optics, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun, Jilin 130033 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Lu, Qipeng, E-mail: Luqipeng51@126.com [State Key Laboratory of Applied Optics, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun, Jilin 130033 (China); Gong, Xuepeng [State Key Laboratory of Applied Optics, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun, Jilin 130033 (China)

    2016-08-01

    The use of atomic hydrogen to clean carbon contaminants on multilayers in extreme ultraviolet lithography systems has been extensively investigated. Additional knowledge of the cleaning rate would not only provide a better understanding of the reaction mechanism but would also inform the industry's cleaning process. In this paper, which focuses on the atomic-hydrogen-based carbon contamination cleaning process, a possible mechanism for the associated reactions is studied and a cleaning model is established. The calculated results are in good agreement with the existing experimental data in the literature. The influences of the main factors – such as activation energy and types of contamination – on the cleaning rate are addressed by the model. The model shows that the cleaning rate depends on the type of carbon contamination. The rate for a polymer-like carbon layer is higher than the rate for graphitic and diamond-like carbon layers. At 340 K, the rate for a polymer-like carbon layer is 10 times higher than for graphitic carbon layers. This model could be used effectively to predict and evaluate the cleaning rates for various carbon contamination types. - Highlights: • Mechanism of H{sup 0} cleaning with C contamination on EUV multilayers is given. • Reflectivity of multilayers rely on various types of C contamination is analyzed. • A model of H{sup 0} cleaning various types of C contamination layers is built. • Accurate predicting and evaluating the rate of H{sup 0} cleaning by the mode is proved. • It would be beneficial for improving H{sup 0} cleaning process of carbon layers.

  4. 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

  5. Features of atomic images reconstructed from photoelectron, Auger electron, and internal detector electron holography using SPEA-MEM

    Energy Technology Data Exchange (ETDEWEB)

    Matsushita, Tomohiro, E-mail: matusita@spring8.or.jp [Japan Synchrotron Radiation Research Institute, SPring-8, Sayo, Hyogo 679-5198 (Japan); Matsui, Fumihiko [Graduate School of Materials Science, Nara Institute of Science and Technology, Ikoma, Nara 630-0192 (Japan)

    2014-08-15

    Highlights: • We develop a 3D atomic image reconstruction algorithm for photoelectron, Auger electron, and internal detector holography. • We examine the shapes of the atomic images reconstructed by using a developed kernel function. • We examine refraction effect at surface, limitation effect of the hologram data, energy resolution effect, and angular resolution effect. • These discussions indicate the experimental requirements to obtain the clear 3D atomic image. - Abstract: Three-dimensional atomic images can be reconstructed from photoelectron, Auger electron, and internal detector electron holograms using a scattering pattern extraction algorithm using the maximum entropy method (SPEA-MEM) that utilizes an integral transform. An integral kernel function for the integral transform is the key to clear atomic image reconstruction. We composed the kernel function using a scattering pattern function and estimated its ability. Image distortion caused by multiple scattering was also evaluated. Four types of Auger electron wave functions were investigated, and the effect of these wave function types was estimated. In addition, we addressed refraction at the surface, the effects of data limitation, and energy and angular resolutions.

  6. Evaluation of Performance Catalytic Ozonation Process with Activated Carbon in the Removal of Humic Acids from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Gh. Asgari

    2011-01-01

    Full Text Available Introduction & Objective: In recent years, the use of alternative disinfectants and the control of natural organic matters are two approaches that are typically applied in water treatment utilities to reduce the formation of chlorinated disinfection by-products. Catalytic ozonation is a new technology used to promote the efficiency of ozonation. The goal of this study was to survey the feasibility application of activated carbon as a catalyst in ozonation process for removal of humic acids from aqueous solution. Materials & Methods: This experimental study has been done in laboratory of water and wastewater chemistry, Tarbiat Modarres University. The solid structure and chemical composition of activated carbon were analyzed by X-ray fluorescence (XRF. Ozonation and catalytic ozonation experiments were performed in a semi-batch reactor and the mass of ozone produced was measured by iodometric titration methods. Concentration changes of humic acid in samples with a concentration of 15 mg/l were determined by using spectrophotometer at an absorbance wavelength of 254 nm. To evaluate the performance of catalytic ozonation in humic acid removal, total organic carbon and trihalomethane formation potential were evaluated and the results were analyzed by Excel software. Results: Catalytic ozone results showed that using activated carbon as a catalyst increased humic acid decomposition up to 11 times and removal efficiency increased with increasing pH (4-12 and catalyst dosage (0.25-1.5 g/250cc. The experimental results showed that catalytic ozonation was most effective in less time (10 min with considerable efficiency (95% compared to the sole ozonation process (SOP. Conclusion: The results indicated that the catalytic ozonation process, compared to SOP, was less affected by radical scavenger, and total organic carbon, and trihalomethane formation potential removal achieved were 30% and 83%, respectively. (Sci J Hamadan Univ Med Sci 2011;17(4:25-33

  7. 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. Copyright © 2015 Elsevier Ltd. All rights reserved.

  8. Hydrothermal atomic force microscopy observations of barite step growth rates as a function of the aqueous barium-to-sulfate ratio

    Science.gov (United States)

    Bracco, Jacquelyn N.; Gooijer, Yiscka; Higgins, Steven R.

    2016-06-01

    The rate of growth of ionic minerals from solutions with varying aqueous cation:anion ratios may result in significant errors in mineralization rates predicted by commonly-used affinity-based rate equations. To assess the potential influence of solute stoichiometry on barite growth, step velocities on the barite (0 0 1) surface have been measured at 108 °C using hydrothermal atomic force microscopy (HAFM) at moderate supersaturation and as a function of the aqueous barium:sulfate ratio (r). Barite growth hillocks at r ∼ 1 were bounded by steps, however at r , and the [0 1 0] steps developed. At r > 1, steps roughened and rounded as the kink site density increased. Step velocities peaked at r = 1 and decreased roughly symmetrically as a function of r, indicating the attachment rates of barium and sulfate ions are similar under these conditions. We hypothesize that the differences in our observations at high and low r arise from differences in the attachment rate constants for the obtuse and acute steps. Based on results at low r, the data suggests the attachment rate constant for barium ions is similar for obtuse and acute steps. Based on results at high r, the data suggests the attachment rate constant for sulfate is greater for obtuse steps than acute steps. Utilizing a step growth model developed by Stack and Grantham (2010) the experimental step velocities as a function of r were readily fit while attempts to fit the data using a model developed by Zhang and Nancollas (1998) were less successful.

  9. Adsorption of methylene blue from aqueous solution onto activated carbons developed from eucalyptus bark and Crataegus oxyacantha core.

    Science.gov (United States)

    Zazouli, Mohammad Ali; Azari, Ali; Dehghan, Samaneh; Salmani Malekkolae, Razieh

    2016-11-01

    In this study, eucalyptus bark and Crataegus oxyacantha core-based activated carbon were synthesized and their morphological features characterized by scanning electron microscopy and Fourier transform infrared spectroscopy techniques. The efficiency of synthesized adsorbents in removal of methylene blue (MB) from aqueous solution was investigated in a series of batch experiments. Furthermore, the influences of various experimental factors involving the contact time, the initial dye concentration, the adsorbent dosage, and the pH of the dye solution were investigated. The point of zero charge (pHpzc) of the applied adsorbents was also determined. In addition, the experimental data were expressed by Langmuir, Freundlich and Tempkin isotherms and pseudo-first order and pseudo-second order kinetic models. Adsorption equilibrium of the two adsorbents was reached within 1 h for MB concentrations of 20 to 100 mg/L. The equilibrium data obtained at optimum conditions of MB sorption by eucalyptus bark activated carbon and Crataegus oxyacantha core activated carbon were best fitted to Tempkin and Langmuir isotherm models, respectively. Besides, it was revealed that the adsorption rate follows a pseudo-second order kinetic model. From the findings of this study, it can be postulated that these adsorbents could be of great potential as a new class of adsorbents for organic dye removal from polluted water.

  10. Removal of copper (II from aqueous solutions by adsorption onto granular activated carbon in the presence of competitor ions

    Directory of Open Access Journals (Sweden)

    Saeed Almohammadi

    2016-04-01

    Full Text Available In this work, the removal of copper from an aqueous solution by granular activated carbon (GAC in the presence of competitor ions was studied. A batch adsorption was carried out and different parameters such as pH, contact time, initial copper concentration and competitor ions concentration were changed to determine the optimum conditions for adsorption. The optimum pH required for maximum adsorption was found to be 4.5 for copper. Equilibrium was evaluated at 144 h at room temperature. The removal efficiency of Cu(II was 71.12% at this time. The kinetics of copper adsorption on activated carbon followed the pseudo second-order model. The experimental equilibrium sorption data were tested using the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D-R equations and the Langmuir model was found to be well fitted for copper adsorption onto GAC. The maximum adsorption capacity of the adsorbent for Cu(II was calculated from the Langmuir isotherm and found to be 7.03 mg/g. Subsequently, the removal of copper by granular activated carbon in the presence of Ag1+ and Mn2+ as competitor ions was investigated. The removal efficiency of Cu(II ions without the presence of the competitor ions was 46% at 6 h, while the removal efficiency of Cu(II ions in the presence of competitor ions, Ag1+ and Mn2+ , was 34.76% and 31.73%, respectively.

  11. Kinetics and Thermodynamics of Sorption of 4-Nitrophenol on Activated Kaolinitic Clay and Jatropha Curcas Activated Carbon from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Samsudeen Olanrewaju Azeez

    2016-06-01

    Full Text Available Adsorption behaviour of 4-nitrophenol (4-NP on activated kaolinitic clay and Jatropha curcas activated carbon was investigated. The kaolinitic clay and Jatropha curcas were activated with 1 M HNO3 and 0.5 M NaOH respectively and were characterized by XRF, XRD, BET, SEM and FTIR techniques. The effects of processing parameters, such as initial 4-NP concentration, temperature, pH, contact time and adsorbent dosage on the adsorption process were investigated. The results obtained showed that Jatropha curcas activated carbon exhibited higher performance than activated kaolinitic clay for the removal of 4-nitrophenol from aqueous solution. Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models were used to describe the adsorption isotherms. The adsorption data were best fitted with Freundlich model. The experimental data of the two adsorbate-adsorbent systems fitted very well with the pseudo-second order kinetic model with r2 values of 0.999 respectively. Adsorption thermodynamic parameters were also estimated. The results revealed that the adsorption of 4-nitrophenol onto both adsorbents were exothermic processes and spontaneous for Jatropha curcas activated carbon but non spontaneous for activated kaolinitic clay.

  12. Utilization of Pine Nut Shell derived carbon as an efficient alternate for the sequestration of phthalates from aqueous system

    Directory of Open Access Journals (Sweden)

    Umair A. Qureshi

    2014-12-01

    Full Text Available This study highlights the importance of a cheap bio waste; Pine Nut Shell (PNS, from which a carbon is synthesized that can efficiently remove toxic phthalates from an aqueous system. PNS derived carbon shows high affinity toward phthalates in descending order along with adsorption capacity i.e., dibutyl phthalate (DBP 5.65 mg/g > diallyl phthalate (DAP 3.64 mg/g > diethyl phthalate (DEP and 2.87 mg/g > dimethyl phthalate (DMP 2.48 mg/g. Different characterization techniques such as FTIR, elemental analysis, point of zero electric charge (PZC, SEM, EDX and BET were employed to investigate the binding sites and surface area of the adsorbent. Adsorption experiments were performed both in batch and column modes. Equilibrium studies showed that the Langmuir isotherm fits best to experimental data. Kinetically, adsorption phenomena obeyed pseudo second order. Furthermore, thermodynamic results expressed the exothermic nature of adsorption on the basis of negative value of enthalpy change. Column sorption method was also adapted to check the feasibility of the adsorption process through the investigation of flow rate, breakthrough curve and pre-concentration factor which is found to be 13 for DMP and DEP and 16 for DAP and DBP. Methanol was found to be best solvent for the recovery of phthalates. Application in real water samples also showed good efficiency of PNS derived carbon for the removal of phthalates.

  13. Non-aqueous carbon black suspensions for lithium-based redox flow batteries: rheology and simultaneous rheo-electrical behavior.

    Science.gov (United States)

    Youssry, Mohamed; Madec, Lénaïc; Soudan, Patrick; Cerbelaud, Manuella; Guyomard, Dominique; Lestriez, Bernard

    2013-09-14

    We report on the rheological and electrical properties of non-aqueous carbon black (CB) suspensions at equilibrium and under steady shear flow. The smaller the primary particle size of carbon black is, the higher the magnitude of rheological parameters and the conductivity are. The electrical percolation threshold ranges seem to coincide with the strong gel rather than the weak gel rheological threshold ones. The simultaneous measurements of electrical properties under shear flow reveal the well-known breaking-and-reforming mechanism that characterises such complex fluids. The small shear rate breaks up the network into smaller agglomerates, which in turn transform into anisometric eroded ones at very high shear rates, recovering the network conductivity. The type of carbon black, its concentration range and the flow rate range are now precisely identified for optimizing the performance of a redox flow battery. A preliminary electrochemical study for a composite anolyte (CB/Li4Ti5O12) at different charge-discharge rates and thicknesses is shown.

  14. Different effects of surface heterogeneous atoms of porous and non-porous carbonaceous materials on adsorption of 1,1,2,2-tetrachloroethane in aqueous environment.

    Science.gov (United States)

    Chen, Weifeng; Ni, Jinzhi

    2017-05-01

    The surface heterogeneous atoms of carbonaceous materials (CMs) play an important role in adsorption of organic pollutants. However, little is known about the surface heterogeneous atoms of CMs might generate different effect on adsorption of hydrophobic organic compounds by porous carbonaceous materials - activated carbons (ACs) and non-porous carbonaceous materials (NPCMs). In this study, we observed that the surface oxygen and nitrogen atoms could decrease the adsorption affinity of both ACs and NPCMs for 1,1,2,2-tetrachloroethane (TeCA), but the degree of decreasing effects were very different. The increasing content of surface oxygen and nitrogen ([O + N]) caused a sharper decrease in adsorption affinity of ACs (slope of lg (k d /SA) vs [O + N]: -0.098∼-0.16) than that of NPCMs (slope of lg (k d /SA) vs [O + N]: -0.025∼-0.059) for TeCA. It was due to the water cluster formed by the surface hydrophilic atoms that could block the micropores and generate massive invalid adsorption sites in the micropores of ACs, while the water cluster only occupied the surface adsorption sites of NPCMs. Furthermore, with the increasing concentration of dissolved TeCA, the effect of surface area on adsorption affinity of NPCMs for TeCA kept constant while the effect of [O + N] decreased due to the competitive adsorption between water molecule and TeCA on the surface of NPCMs, meanwhile, both the effects of micropore volume and [O + N] on adsorption affinity of ACs for TeCA were decreased due to the mechanism of micropore volume filling. These findings are valuable for providing a deep insight into the adsorption mechanisms of CMs for TeCA. Copyright © 2017 Elsevier Ltd. All rights reserved.

  15. Sorption of nickel (II) from aqueous system by chemically modified pungan (pongamia pinnata) seedpod carbon

    Science.gov (United States)

    Senthil, M.; Arulanantham, A.

    2013-06-01

    The adsorption of Ni (II) on chemically modified bicarbonate impregnated sulphuric acid treated pungan (pongamia pinnata) seedpod carbon (BSPAC) was investigated as a function of equilibrium time, solution pH and carbon dosage. The adsorption of nickel (II) was also studied by using Freundlich, Langmuir and Temkin isotherm models. Kinetic studies were conducted using reversible-first-order, pseudo-first-order and pseudo-second-order kinetic equations. The results obtained were compared with commercially available activated carbon (CAC) of same 20-50 ASTM mesh size.

  16. Adsorption of pharmaceutical compounds and an endocrine disruptor from aqueous solutions by carbon materials.

    Science.gov (United States)

    Sotelo, José L; Rodríguez, Araceli R; Mateos, María M; Hernández, Sergio D; Torrellas, Silvia A; Rodríguez, Juan G

    2012-01-01

    Adsorption has been used to study the removal of atenolol, caffeine, diclofenac and isoproturon, pharmaceutical compounds as emerging contaminants and an endocrine disruptor from ultrapure water and a municipal wastewater treatment plant effluent with three carbonaceous materials: activated carbon, multiwalled carbon nanotubes and carbon nanofibers. The adsorption capacities were studied in the temperature range of 25-65°C and pH range from 3 to 9. Several model isotherms were used to model the adsorption equilibrium data. Also, the competitive adsorption was evaluated.

  17. Metal Oxide-Carbon Nanocomposites for Aqueous and Nonaqueous Supercapacitors Project

    Data.gov (United States)

    National Aeronautics and Space Administration — This Small Business Technology Transfer Phase 2 effort focuses on development of a supercapacitor energy storage device based on novel metal oxide-carbon...

  18. An effective route for the room temperature formation of Pd coatings on multiwalled carbon nanotubes in aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Yeong Joon [Dept. of Chemistry, Chungnam National University, Daejeon (Korea, Republic of); Lee, Im Kyu; Song, Jae Hee [Dept. of Chemistry, Sunc hon National University, Suncheon (Korea, Republic of)

    2016-10-15

    We present an easy one-pot synthesis route for the production of palladium nanoparticles and multiwalled carbon nanotubes (MWCNTs)-supported Pd-nanomaterial composites by a simple proton beam irradiation process in an aqueous solution at room temperature. Pristine and surface-modified MWCNTs were used to prepare MWCNT–Pd hybrids. Pd nanoparticles on the surfaces of MWCNTs were produced in situ in an aqueous solution without the addition of any harsh reducing agent. Pristine and thiolated MWCNTs were both densely decorated with spherical Pd nanoparticles and eventually Pd nanowire formation on MWCNTs was realized when reaction times exceeded 60 min. The thicknesses of Pd coatings on MWCNT surfaces were controlled by varying the concentration of MWCNTs in the reaction mixture. MWCNT-Pd composites were characterized by time-resolved transmission electron microscopy, selected area electron diffraction, and energy dispersive X-ray spectroscopy, and the results obtained showed that Pd coatings were continuous, and resulted in a MWCNT-supported Pd nanowire structure.

  19. Rapid Removal of Zinc(II) from Aqueous Solutions Using a Mesoporous Activated Carbon Prepared from Agricultural Waste.

    Science.gov (United States)

    Zhang, Xiaotao; Hao, Yinan; Wang, Ximing; Chen, Zhangjing

    2017-08-28

    A low-cost activated carbon (XSBLAC) prepared from XanthocerasSorbifoliaBungehull via chemical activation was investigated to determine its adsorption and desorption properties for zinc(II) ions from aqueous solutions. XSBLAC was characterized based on its N₂-adsorption/desorption isotherm, EDX, XRD, SEM and FTIR results. An adsorption study was conducted in a series of experiments to optimize the process variables for zinc(II) removal using XSBLAC. Modeling the adsorption kinetics indicated good agreement between the experimental data and the pseudo-second-order kinetic model. The Langmuir equilibrium isotherm fit the experimental data reasonably well. The calculated enthalpy (ΔH⁰), entropy (ΔS⁰) and Gibbs free energy (ΔG⁰) values revealed the endothermic and spontaneous nature of the adsorption process. HNO₃ displayed the best desorption performance. The adsorption mechanism was investigated in detail through FTIR and SEM/EDX spectroscopic analyses. The results suggested that XSBLAC is a potential biosorbent for removing zinc(II) from aqueous solutions.

  20. Flame Atomic Absorption Determination of Gold Ion in Aqueous Samples after Preconcentration Using 9-Acridinylamine Functionalized γ-Alumina Nanoparticles

    Directory of Open Access Journals (Sweden)

    Mohammad Karimi

    2013-01-01

    Full Text Available A simple and sensitive solid phase extraction utilizing 9-acridinylamine functionalized alumina nanoparticles was developed, and their potential use for preconcentration and subsequent determination of gold by flame atomic absorption spectrometry (FAAS was investigated. A number of parameters, namely, type, concentration, and volume of eluent, pH of the sample solution, flow rate of extraction, and volume of the sample, were evaluated. The effect of a variety of ions on preconcentration and recovery was also investigated. Gold ions were found to be recovered quantitatively at pH 3.0, with 0.1 mol L−1 thiourea in 2 mol L−1 H2SO4 as eluent. The limit of detection (LOD, defined as five times the standard deviation of the blank, was determined to be lower than 13.0 ppb. Under optimum conditions, the accuracy and precision (RSD% of the method were >98.0 and <1.5%, respectively. To gauge its ability in terms of application to real samples, the proposed method was successfully applied for determination of gold concentration in waste water samples and one soil standard material, and satisfactory results were obtained.

  1. Updated Mortality Analysis of Radiation Workers at Rocketdyne (Atomics International), 1948-2008

    Energy Technology Data Exchange (ETDEWEB)

    Boice Jr JD, Colen SS, Mumma MT, Ellis ED, Eckerman DF, Leggett RW, Boecker BB, Brill B, Henderson BE

    2011-08-01

    Updated analyses of mortality data are presented on 46,970 workers employed 1948-1999 at Rocketdyne (Atomics International). Overall, 5,801 workers were involved in radiation activities, including 2,232 who were monitored for intakes of radionuclides, and 41,169 workers were engaged in rocket testing or other non-radiation activities. The worker population is unique in that lifetime occupational doses from all places of employment were sought, updated and incorporated into the analyses. Further, radiation doses from intakes of 14 different radionuclides were calculated for 16 organs or tissues using biokinetic models of the International Commission on Radiation Protection (ICRP). Because only negligible exposures were received by the 247 workers monitored for radiation activities after 1999, the mean dose from external radiation remained essentially the same at 13.5 mSv (maximum 1 Sv) as reported previously, as did the mean lung dose from external and internal radiation combined at 19.0 mSv (maximum 3.6 Sv). An additional 9 years of follow-up, from December 31,1999 through 2008, increased the person-years of observation for the radiation workers by 21.7% to 196,674 (mean 33.9 years) and the number of cancer deaths by 50% to 684. Analyses included external comparisons with the general population and the computation of standardized mortality ratios (SMRs) and internal comparisons using proportional hazards models and the computation of relative risks (RRs). A low SMR for all causes of death (SMR 0.82; 95% CI 0.78-0.85) continued to indicate that the Rocketdyne radiation workers were healthier than the general population and were less likely to die. The SMRs for all cancers taken together (SMR 0.88; 95% CI 0.81-0.95), lung cancer (SMR 0.87; 95% CI 0.76-1.00) and leukemia other than chronic lymphocytic leukemia (CLL) (SMR 1.04; 95% 0.67-1.53) were not significantly elevated. Cox regression analyses revealed no significant dose-response trends for any cancer. For all

  2. Hydrodynamic and absorption studies of carbon dioxide absorption in aqueous amide solutions using a bubble column contactor

    Directory of Open Access Journals (Sweden)

    A. Blanco

    2013-12-01

    Full Text Available The present work analyses the carbon dioxide absorption process in aqueous n-alkylpyrrolidones solutions, from the point of view of hydrodynamic studies as well as mass transfer, using a bubble column contactor. An analysis of the influence of solute concentration and gas flow-rate is complemented by the study of the effect caused by the alkyl group on the hydrodynamics and mass transfer. The presence of this kind of substance produces a decrease in mass transfer rate, but on the basis of interfacial area and mass transfer coefficient values, ethyl-2-pyrrolidine (EP shows suitable characteristics to replace methyl-2-pyrrolidine (MP in gas separation processes due to its lower safety problems.

  3. Kinetics of the Removal of Chromium Complex Dye from Aqueous Solutions Using Activated Carbons and Polymeric Adsorbent

    Directory of Open Access Journals (Sweden)

    Eglė Kazlauskienė

    2011-04-01

    Full Text Available 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 found relatively higher than that using AC. The pseudo-second order and intraparticle diffusion models agreed well with experimental data. The parameters of these models were studied as a function of temperature and adsorbent nature.Article in Lithuanian

  4. Equilibrium and kinetics study on the adsorption of perfluorooctanoic acid from aqueous solution onto powdered activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Qu Yan [State Key Laboratory of Pollution Control and Resource Ruse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Zhang Chaojie, E-mail: myrazh@mail.tongji.edu.cn [State Key Laboratory of Pollution Control and Resource Ruse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Li Fei [State Key Laboratory of Pollution Control and Resource Ruse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China); Bo Xiaowen [College of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Liu Guangfu; Zhou Qi [State Key Laboratory of Pollution Control and Resource Ruse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China)

    2009-09-30

    Powdered activated carbon (PAC) was applied to remove perfluorooctanoic acid (PFOA) from the aqueous PFOA solution in this study. Contact time, adsorbent dose and temperature were analyzed as the effect factors in the adsorption reaction. The contact time of maximum PFOA uptake was around 1 h while the sorption removal efficiency increased with the PAC concentrations. And the process of adsorption increased from 303 K to 313 K and then decreased from 313 K to 323 K. Among four applied models, the experimental isotherm data were discovered to follow Langmuir isotherm model more closely. Thermodynamically, adsorption was endothermic because enthalpy, entropy and Gibbs constants were 198.5 kJ/mol, 0.709 kJ/mol/K and negative, respectively, which also indicated that the adsorption process was spontaneous and feasible. From kinetic analysis, the adsorption was suggested to be pseudo-second-order model. The adsorption of PFOA on the PAC was mainly controlled by particle diffusion.

  5. Preparation of Activated Carbon From Polygonum orientale Linn. to Remove the Phenol in Aqueous Solutions.

    Directory of Open Access Journals (Sweden)

    Jia Feng

    Full Text Available Phenol components are major industry contaminants of aquatic environment. Among all practical methods for removing phenol substances from polluted water, activated carbon absorption is the most effective way. Here, we have produced low-cost activated carbon using Polygonum orientale Linn, a wide spreading species with large biomass. The phenol adsorption ability of this activated carbon was evaluated at different physico-chemical conditions. Average equilibrium time for adsorption was 120 min. The phenol adsorption ability of the P. orientale activated carbon was increased as the pH increases and reached to the max at pH 9.00. By contrast, the ionic strength had little effect on the phenol absorption. The optimum dose for phenol adsorption by the P. orientale activated carbon was 20.00 g/L. The dominant adsorption mechanism of the P. orientale activated carbon was chemisorption as its phenol adsorption kinetics matched with the pseudo-second-order kinetics. In addition, the equilibrium data were fit to the Langmuir model, with the negative standard free energy and the positive enthalpy, suggesting that adsorption was spontaneous and endothermic.

  6. Thermodynamic Properties of Aqueous Carbonate Species and Solid Carbonate Phases of Selected Trace Elements pertinent to Drinking Water Standards of the U.S. Environmental Protection Agency

    Energy Technology Data Exchange (ETDEWEB)

    Apps, John A. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Wilkin, Richard T. [US Environmental Protection Agency (EPA), Cincinnati, OH (United States)

    2015-09-30

    This report contains a series of tables summarizing the thermodynamic properties of aqueous carbonate complexes and solid carbonate phases of the following elements: arsenic (As), barium (Ba), cadmium (Cd), chromium (Cr), cobalt (Co), copper (Cu), iron (Fe), lead (Pb), manganese (Mn), mercury (Hg), nickel (Ni) thallium (Tl), uranium (U) and zinc (Zn). Most of these elements are potentially hazardous as defined by extant primary drinking water standards of the United States Environmental Protection Agency (EPA). The remainder are not considered hazardous, but are either listed by EPA under secondary standards, or because they can adversely affect drinking water quality. Additional tables are included giving the thermodynamic properties for carbonates of the alkali metal and alkali earth elements, sodium (Na), potassium (K), magnesium (Mg), calcium (Ca), and strontium (Sr), because of their value in developing correlative models to estimate the thermodynamic properties of carbonate minerals for which no such data currently exist. The purpose in creating the tables in this report is to provide future investigators with a convenient source for selecting and tracing the sources of thermodynamic data of the above listed elements for use in modeling their geochemical behavior in “underground sources of drinking water” (USDW). The incentive for doing so lies with a heightened concern over the potential consequences of the proposed capture and storage of carbon dioxide (CO2) generated by fossil fuel fired power plants in deep subsurface reservoirs. If CO2 were to leak from such reservoirs, it could migrate upward and contaminate USDWs with undesirable, but undetermined, consequences to water quality. The EPA, Office of Research and Development, through an Interagency Agreement with the U.S. Department of Energy at the Lawrence Berkeley National Laboratory, funded the preparation of this report.

  7. Effects of Aqueous Mineral Carbonation on Deformation and Transport Properties in Dunite

    Science.gov (United States)

    Lisabeth, H. P.; Zhu, W.; Kelemen, P. B.

    2012-12-01

    Carbon dioxide is one of the most common geologic fluids resulting from volcanic as well as diagenetic activity. Proposed carbon sequestration initiatives may result in locally high concentrations of carbon dioxide in various reservoirs; however, the effect of dissolved carbon dioxide in pore water on the mechanical behavior and transport property evolution of earth materials at upper crustal conditions is poorly constrained. These effects can take the form of complex chemical and mechanical feedbacks. To begin exploring these processes we have performed hydrostatic compaction, constant strain rate deformation and constant stress creep experiments on thermally cracked dunite saturated with either distilled water or carbon dioxide-rich brine and measured the mechanical strain and concomitant permeability changes throughout the experiments. The suite of experiments was carried out at 150°C with 15 MPa confining pressure and pore pressure held constant at 10 MPa. Deformations were performed at a constant strain rate of 10-5s-1. At all conditions, experiments with carbon dioxide-rich brine as pore fluid exhibited enhanced compaction and permeability reduction compared to those with distilled water. In hydrostatic tests, carbon dioxide-rich brine increased the rate of compaction by half an order of magnitude and reduced permeability by an order of magnitude. During deformation all samples showed stress induced dilatancy due to microcracking, although samples saturated with carbon dioxide-rich brine exhibited enhanced compaction compared to samples saturated with distilled water. After loaded beyond the onset of dilatancy, C', samples were held at a constant differential stress of ~110 MPa (~85% of peak load) and time-dependent creep behavior was observed. During the time-dependent portion of the tests, samples saturated with carbon dioxide-rich fluids exhibited modest dilatancy and enhanced permeability reduction when compared to samples saturated with distilled water

  8. Novel atomic force microscope cantilevers and piezoresistance of carbon nanotubes and germanium nanowires

    Science.gov (United States)

    Grow, Randal James

    2005-11-01

    There has been great interest in recent years in nanometer-scale materials and tools for fabricating and characterizing them. One such tool is the atomic force microscope (AFM), which has developed rapidly since its invention in 1986. Imaging soft or fragile samples with AFM requires low-spring-constant cantilevers to minimize the force on the sample. Silicon nitride is well suited to making such soft cantilevers, but it is not ideal for making sharp tips. We combined a silicon nitride cantilever with a sharp silicon tip to achieve a hybrid with both a low spring constant and a sharp tip. Carbon nanotubes have received great attention for their remarkable mechanical and electrical properties. Their electromechanical properties are also interesting, as a few groups have determined by deforming suspended nanotubes. Their change in resistance under strain is stronger than that of silicon, which is commonly used in mechanical sensors. However, the fragility of suspended tubes makes them impractical for mass-produced sensors. Tubes on surfaces are more robust. We fabricated micromachined pressure sensors using a thin silicon nitride membrane with metal-contacted carbon nanotubes on the surface. Deforming the membrane with gas pressure stretched the nanotube, and we measured the resistance changes. They were stronger than those of suspended nanotubes, probably because of local deformations in the nanotube caused by interaction with the surface. Nanowires of semiconductors such as silicon and germanium have also evoked much interest for electronics and optics applications. The piezoresistive effect in nanowires should also be larger than that of the bulk material, which could be useful for increasing the sensitivity of mechanical sensors or for enhancing the performance of nanowire transistors. We have fabricated pressure sensors with germanium nanowires as the sensing elements, and we have found the piezoresistance to be much stronger than in the bulk. We understand this

  9. Study On Adsorption of Bromate From Aqueous Solution On Modified Activated Carbon

    Science.gov (United States)

    Liu, Tong-mian; Cui, Fu-yi; Zhao, Zhi-wei; Liu, Dong-mei; Zhu, Qi; Wang, Huan

    2010-11-01

    A coal-based activated carbon was treated chemically with nitric acid, sodium hydroxide and ammonia for its surface modification, and its adsorption capacity was investigated with bromate. Several techniques were used to characterize the physicochemical properties of these materials including BET, XPS, pHpzc and Boehm titration. The results indicated that the specific surface area of the activated carbon decreased after oxidation with nitric acid. But the amount of surface acidic oxygen-containing functional groups of the oxidized sample increased compared to the raw carbon and the points of zero charge (pHpzc) decreased. The specific surface area of the activated carbon also decreased after sodium hydroxide treatment and the points of zero charge increased. The changes of surface chemical properties after the ammonia treatment was opposite to the oxidized sample. As a result, the pHpzc of the carbon was increased to near pH9.3, the amount of surface basic groups was increased. Furthermore, the data of bromate adsorption on all the samples were fitted to the Langmuir isotherm model well which indicates monolayer adsorption. In addition, the adsorption capacity of ammonia treatment sample was the highest and its saturated adsorption capacity reached 1.55 mg/g. A strong correlation was found between basic groups and adsorption capacity of bromate. Enhancement of basic groups was favorable for bromate removal.

  10. Evaluation of carbon nanotube probes in critical dimension atomic force microscopes

    Science.gov (United States)

    Choi, Jinho; Park, Byong Chon; Ahn, Sang Jung; Kim, Dal-Hyun; Lyou, Joon; Dixson, Ronald G.; Orji, Ndubuisi G.; Fu, Joseph; Vorburger, Theodore V.

    2016-07-01

    The decreasing size of semiconductor features and the increasing structural complexity of advanced devices have placed continuously greater demands on manufacturing metrology, arising both from the measurement challenges of smaller feature sizes and the growing requirement to characterize structures in more than just a single critical dimension. For scanning electron microscopy, this has resulted in increasing sophistication of imaging models. For critical dimension atomic force microscopes (CD-AFMs), this has resulted in the need for smaller and more complex tips. Carbon nanotube (CNT) tips have thus been the focus of much interest and effort by a number of researchers. However, there have been significant issues surrounding both the manufacture and use of CNT tips. Specifically, the growth or attachment of CNTs to AFM cantilevers has been a challenge to the fabrication of CNT tips, and the flexibility and resultant bending artifacts have presented challenges to using CNT tips. The Korea Research Institute for Standards and Science (KRISS) has invested considerable effort in the controlled fabrication of CNT tips and is collaborating with the National Institute of Standards and Technology on the application of CNT tips for CD-AFM. Progress by KRISS on the precise control of CNT orientation, length, and end modification, using manipulation and focused ion beam processes, has allowed us to implement ball-capped CNT tips and bent CNT tips for CD-AFM. Using two different generations of CD-AFM instruments, we have evaluated these tip types by imaging a line/space grating and a programmed line edge roughness specimen. We concluded that these CNTs are capable of scanning the profiles of these structures, including re-entrant sidewalls, but there remain important challenges to address. These challenges include tighter control of tip geometry and careful optimization of scan parameters and algorithms for using CNT tips.

  11. Inhibiting properties and adsorption of an amine based fatty acid corrosion inhibitor on carbon steel in aqueous carbon dioxide solutions

    Energy Technology Data Exchange (ETDEWEB)

    Buchweishaija, Joseph

    1997-12-31

    Carbon dioxide corrosion is a major corrosion problem in oil and gas production systems and many organic inhibitors have been tested and used to protect the substrate from corrosion. This thesis studies the mechanism of interaction of the inhibitor molecule with the metallic substrate and how this affects the dissolution rate of the metal. The performance of a commercial amine based fatty acid corrosion inhibitor has been investigated using rotating cylinder electrodes and carbon steel electrodes in CO{sub 2} saturated formation water in the temperature range between 35 to 80{sup o}C. The corrosion process was monitored by electrochemical impedance measurements, and at the end of each experiment full polarization curves were recorded. When the inhibitor was applied on noncorroded electrodes, high inhibitor performance, over 99.7%, was observed independent of temperature. On precorroded electrodes inhibitor performance was found to depend on temperature and time of precorrosion. Above 60{sup o}C, the inhibitor performance decreased with increasing time of precorrosion, presumably because of the formation of a corrosion film of either iron carbonate or a combination of iron carbonate and iron carbide which prevent the inhibitor from reaching the surface. The inhibitor protection efficiency was assumed to be associated with the degree of inhibitor coverage at the material surface, and adsorption isotherms have been calculated in the concentration range between 0.1 ppm and 100 ppm. A Langmuir isotherm was found to give the best fit. The inhibitor performance on a 2 days precorroded rotating electrode was investigated at different solution pH ranging between 4.5 and 6.5 at 35{sup o}C. 130 refs., 80 figs., 22 tabs.

  12. Tumor radiosensitizers - current status of development of various approaches: Report of an International Atomic Energy Agency meeting

    DEFF Research Database (Denmark)

    Horsman, Michael Robert; Bohm, Lothar; Margison, Geoffrey P.

    2006-01-01

    PURPOSE: The International Atomic Energy Agency (IAEA) held a Technical Meeting of Consultants to (1) discuss a selection of relatively new agents, not those well-established in clinical practice, that operated through a variety of mechanisms to sensitize tumors to radiation and (2) to compare...... and contrast their tumor efficacy, normal tissue toxicity, and status of development regarding clinical application. The aim was to advise the IAEA as to which developing agent or class of agents would be worth promoting further, by supporting additional laboratory research or clinical trials...... and for clinical trials that would be suitable for industrialized countries, as well as trials that were considered more appropriate for developing countries.PURPOSE: The International Atomic Energy Agency (IAEA) held a Technical Meeting of Consultants to (1) discuss a selection of relatively new agents, not those...

  13. Effect of Fe ion concentration on fatigue life of carbon steel in aqueous CO2 environment

    DEFF Research Database (Denmark)

    Rogowska, Magdalena; Gudme, J.; Rubin, A.

    2016-01-01

    In this work, the corrosion fatigue behaviour of steel armours used in the flexible pipes, in aqueous solutions initially containing different concentrations of Fe2+, was investigated by four-point bending testing under saturated 1 bar CO2 condition. Corrosion fatigue results were supported with ex...... situ measurements of Fe2+ and pH. Characterisation of the corrosion scales and crack formations was performed using microscopic and diffraction techniques. Fatigue results showed two times better fatigue life, at the stress ranges of 250 MPa, for samples tested in solutions containing the concentration...... of Fe2+ marginally above the solubility limit of FeCO3 compared to the samples tested in highly supersaturated solution of Fe2+. Results revealed that the impact of the alternating stresses on the corrosion behaviour of samples reduces with lowering the applied stresses. At the stress range of 100 MPa...

  14. Haloxylon Activated Carbon; a Novel Absorbent to Remove Phenol from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Miranzadeh M.B.* PhD,

    2016-09-01

    Full Text Available Abstract Aims: Even low concentrations of phenol in industrial waste can cause many difficulties for the aquatic environment. So removal of this organic matter is an important issue. the adsorption process, is one of the most effective methods for isolation and purification of Phenols. The aim of this study was to introduce wood haloxylon as a natural and new absorbent to remove phenol from aqueous solutions. Instrument & Methods: Experiments were carried out in laboratory scale to evaluate the effect of important variables such as initial pH (4, 5, 6, 7, 8 and 9, the initial concentration of phenol (100, 50 and 150mg/l, adsorbent dosage (0.5, 1 and 2g/l and reaction time (20, 40 and 60min. The concentration of phenol was measured by the photometric method at wavelengths of 500nm. Findings: The highest efficiency was recorded at pH=7 and at a rate of 45.2% and after it the removal efficiency dropped. The maximum adsorption of phenol happened in the first 20 minutes (35.8% and after that, it was absorbed more slowly and took 60 minutes (45.2% to reach the equilibrium. By increasing the concentration of phenol from 50 to 150mg/l, the removal of phenol reduced from 45.2 to 30.6% and the absorptive capacity increased of from 1.1 to 2.3mg/g. By increasing the adsorbent dosage from 0.5 to 2g/l, the removal of phenol increased from 19.1 to 45.2% and the absorptive capacity decreased from 1.9 to 1.1mg/g. Conclusion: HTAC, in optimum conditions, can be used for pre-treatment of aqueous solution containing phenol.

  15. Aqueous dispersions of oligomer-grafted carbon nanomaterials with controlled surface charge and minimal framework damage

    Science.gov (United States)

    Hu, Sheng; Chen, Shu; Menzel, Robert; Goode, Angela D.; Ryan, Mary P.; Porter, Alexandra E.; Shaffer, Milo S. P.

    2015-01-01

    Functionalised carbon nanomaterials (CNMs), with an undamaged carbon framework and controlled physiochemical properties, are desirable for a wide range of scientific studies and commercial applications. The use of a thermochemical grafting approach provides a versatile means to functionalise both multi-walled carbon nanotubes (MWCNTs) and carbon black (CB) nanoparticles without altering their inherent structure. The functionalisation process was investigated by employing various types of grafting monomers; to improve water solubility, reagents were chosen that introduced ionic character either intrinsically or after further chemical reaction. The degree of grafting for both MWCNTs and CB ranged from 3 to 27 wt%, as established by thermal gravimetric analysis (TGA). Raman spectroscopy confirmed that the structural framework of the MWNTs was unaffected by the thermochemical treatment. The effectiveness of the surface modification was demonstrated by significantly improved dispersibility and stability in water, and further quantified by zeta-potential analysis. The concentration of stable, individualised, grafted MWNTs in water ranged from 30 to 80 µg mL−1, whereas functionalised CB (CB) in water showed improved dispersibility up to ~460 µg mL−1 after centrifugation at 10, 000 g for 15 minutes. The successful preparation of structurally identical but differently functionalised nanoparticles panels, with high water compatibility and minimal framework damage, are useful for controlled experiments. For example, they can be used to explore the relationship between toxicological effects and specific physiochemical properties, such as surface charge and geometry. PMID:25254653

  16. Salinity, dissolved organic carbon and water hardness affect peracetic acid (PAA) degradation in aqueous solutions

    DEFF Research Database (Denmark)

    Liu, Dibo; Steinberg, Christian E.W.; Straus, David L.

    2014-01-01

    -degradation of three commercial products, Wofasteril® E400, Wofasteril® E250 and Wofasteril® Lspez, at a nominal concentration of 1 mg L−1 in relation to two levels of salinity, water hardness, or dissolved organic carbon (DOC). The results showed that salinity and DOC stimulate PAA-degradation, while water hardness...

  17. CO2 Mass transfer model for carbonic anhydrase-enhanced aqueous MDEA solutions

    DEFF Research Database (Denmark)

    Gladis, Arne Berthold; Deslauriers, Maria Gundersen; Neerup, Randi

    2018-01-01

    In this study a CO2 mass transfer model was developed for carbonic anhydrase-enhanced MDEA solutions based on a mechanistic kinetic enzyme model. Four different enzyme models were compared in their ability to predict the liquid side mass transfer coefficient at temperatures in the range of 298...

  18. Competitive adsorption of ibuprofen and amoxicillin mixtures from aqueous solution on activated carbons.

    Science.gov (United States)

    Mansouri, Hayet; Carmona, Rocio J; Gomis-Berenguer, Alicia; Souissi-Najar, Souad; Ouederni, Abdelmottaleb; Ania, Conchi O

    2015-07-01

    This work investigates the competitive adsorption under dynamic and equilibrium conditions of ibuprofen (IBU) and amoxicillin (AMX), two widely consumed pharmaceuticals, on nanoporous carbons of different characteristics. Batch adsorption experiments of pure components in water and their binary mixtures were carried out to measure both adsorption equilibrium and kinetics, and dynamic tests were performed to validate the simultaneous removal of the mixtures in breakthrough experiments. The equilibrium adsorption capacities evaluated from pure component solutions were higher than those measured in dynamic conditions, and were found to depend on the porous features of the adsorbent and the nature of the specific/dispersive interactions that are controlled by the solution pH, density of surface change on the carbon and ionization of the pollutant. A marked roll-up effect was observed for AMX retention on the hydrophobic carbons, not seen for the functionalized adsorbent likely due to the lower affinity of amoxicillin towards the carbon adsorbent. Dynamic adsorption of binary mixtures from wastewater of high salinity and alkalinity showed a slight increase in IBU uptake and a reduced adsorption of AMX, demonstrating the feasibility of the simultaneous removal of both compounds from complex water matrices. Copyright © 2014 Elsevier Inc. All rights reserved.

  19. Potential biodiversity benefits from international programs to reduce carbon emissions from deforestation.

    Science.gov (United States)

    Siikamäki, Juha; Newbold, Stephen C

    2012-01-01

    Deforestation is the second largest anthropogenic source of carbon dioxide emissions and options for its reduction are integral to climate policy. In addition to providing potentially low cost and near-term options for reducing global carbon emissions, reducing deforestation also could support biodiversity conservation. However, current understanding of the potential benefits to biodiversity from forest carbon offset programs is limited. We compile spatial data on global forest carbon, biodiversity, deforestation rates, and the opportunity cost of land to examine biodiversity conservation benefits from an international program to reduce carbon emissions from deforestation. Our results indicate limited geographic overlap between the least-cost areas for retaining forest carbon and protecting biodiversity. Therefore, carbon-focused policies will likely generate substantially lower benefits to biodiversity than a more biodiversity-focused policy could achieve. These results highlight the need to systematically consider co-benefits, such as biodiversity in the design and implementation of forest conservation programs to support international climate policy.

  20. Adsorption of Pb(II) ions from aqueous solutions by date bead carbon activated with ZnCl{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Danish, Mohammed; Hashim, Rokiah; Rafatullah, Mohd; Sulaiman, Othman [Division of Bioresource, Paper and Coatings Technology, School of Industrial Technology, Universiti Sains Malaysia, Penang (Malaysia); Ahmad, Anees [Division of Environmental Technology, School of Industrial Technology, Universiti Sains Malaysia, Penang (Malaysia); Govind [Surface Physics and Nanostructures Group, National Physical Laboratory, New Delhi (India)

    2011-04-15

    This study reports on the adsorption characteristics of Pb(II) ions from aqueous solutions using ZnCl{sub 2}-activated date (Phoenix dactylifera) bead (ADB) carbon with respect to change in adsorbent dosage, initial pH, contact time, initial concentration, and temperature of the solution. Kinetic studies of the data showed that the adsorption follows the pseudo-second-order kinetic model. Thermodynamic parameters, enthalpy change ({Delta}H = 55.11 kJ/mol), entropy change ({Delta}S = - 0.193 kJ/mol/K), and Gibbs free energy change ({Delta}G ) were also calculated for the uptake of Pb(II) ions. These parameters show that adsorption on the surface of ADB was feasible, spontaneous in nature, and endothermic between temperatures of 298.2 and 318.2 K. The equilibrium data better fitted the Langmuir and Freundlich isotherm models than the D-R adsorption isotherm model for studying the adsorption behavior of Pb(II) onto the ADB carbon. It could be observed that the maximum adsorption capacity of ADB was 76.92 mg/g at 318.2 K and pH 6.5. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  1. N-doped nanoporous carbon as efficient catalyst for nitrobenzene reduction in sulfide-containing aqueous solutions.

    Science.gov (United States)

    Liu, Na; Ding, Longzhen; Li, Haijun; Jia, Mingjun; Zhang, Wenxiang; An, Nihong; Yuan, Xiaoling

    2017-03-15

    Metal-free N-doped porous carbon (NC) materials have been demonstrated to be promising catalysts in contaminated environment remediation. Two NC materials (NC-1 and NC-2) were prepared by sol-gel routes. Their catalytic properties were investigated for the reduction of nitrobenzene (NB) in sulfide-containing aqueous solution. Both NC-1 and NC-2 can efficiently catalyze the reduction of NB to aniline (AN) under ambient conditions, but also can be reused for more than 5 times. The reaction fits excellently to the pseudo-first-order kinetic. Compared with NC-1 material, NC-2 shows much higher removal efficiency (rate constant kobs: 0.283h(-1)vs. 2.50h(-1)). The important features of NC material, including high specific surface area, suitable surface functional groups (especially nitrogen-containing groups), and enhanced electron transfer ability, should be mainly factors for its excellent catalytic activity. This work demonstrates that N-doped carbon materials have great potential for degradation of NB to AN in the natural aquatic environment. Copyright © 2016 Elsevier Inc. All rights reserved.

  2. Effective Remediation of Lead Ions from Aqueous Solution by Chemically Carbonized Rubber Wood Sawdust: Equilibrium, Kinetics, and Thermodynamic Study

    Directory of Open Access Journals (Sweden)

    Swarup Biswas

    2015-01-01

    Full Text Available Rubber wood sawdust was carbonized into charcoal by chemical treatment which was used for removal of lead ion from aqueous solution. The work involves batch experiments to investigate the pH effect, initial concentration of adsorbate, contact time, and adsorbent dose. Experimental data confirmed that the adsorption capacities increased with increasing inlet concentration and bed height and decreased with increasing flow rate. Adsorption results showed a maximum adsorption capacity of 37 mg/g at 308 K. Langmuir, Freundlich, and Temkin model adsorption isotherm models were applied to analyze the process where Temkin was found as a best fitted model for present study. Simultaneously kinetics of adsorption like pseudo-first-order, pseudo-second-order, and intraparticle diffusion models were investigated. Thermodynamic parameters were used to analyze the adsorption experiment. Fourier transform infrared spectroscopy, scanning electron microscope, and energy dispersive X-ray spectroscopy confirmed the batch adsorption of lead ion onto chemically carbonized rubber wood sawdust.

  3. Magnetic properties of a single iron atomic chain encapsulated in armchair carbon nanotubes: A Monte Carlo study

    Energy Technology Data Exchange (ETDEWEB)

    Masrour, R., E-mail: rachidmasrour@hotmail.com [Laboratory of Materials, Processes, Environment and Quality, Cady Ayyed University, National School of Applied Sciences, PB 63, 46000 Safi (Morocco); Jabar, A. [Laboratory of Materials, Processes, Environment and Quality, Cady Ayyed University, National School of Applied Sciences, PB 63, 46000 Safi (Morocco); Hamedoun, M. [Institute of Nanomaterials and Nanotechnologies, MAScIR, Rabat (Morocco); Benyoussef, A. [Institute of Nanomaterials and Nanotechnologies, MAScIR, Rabat (Morocco); Hassan II Academy of Science and Technology, Rabat (Morocco); Hlil, E.K. [Institut Néel, CNRS, Université Grenoble Alpes, 25 rue des Martyrs BP 166, 38042 Grenoble cedex 9 (France)

    2017-06-15

    Highlights: • Magnetic properties of Fe atom chain wrapped in armchair carbon nanotubes have been studied. • Transition temperature of iron and carbon have been calculated using Monte Carlo simulations. • The multiples magnetic hysteresis have been found. - Abstract: The magnetic properties have been investigated of FeCu{sub x}C{sub 1−x} for a Fe atom chain wrapped in armchair (N,N) carbon nanotubes (N = 4,6,8,10,12) diluted by Cu{sup 2+} ions using Monte Carlo simulations. The thermal total magnetization and magnetic susceptibility are found. The reduced transition temperatures of iron and carbon have been calculated for different N and the exchange interactions. The total magnetization is obtained for different exchange interactions and crystal field. The Magnetic hysteresis cycles are obtained for different N, the reduced temperatures and exchange interactions. The multiple magnetic hysteresis is found. This system shows it can be used as magnetic nanostructure possessing potential current and future applications in permanent magnetism, magnetic recording and spintronics.

  4. 7th International Workshop on Application of Lasers in Atomic Nuclei Research “Nuclear Ground and Isometric State Properties”

    CERN Document Server

    Błaszczak, Z; Marinova, K; LASER 2006

    2007-01-01

    7th International Workshop on Application of Lasers in Atomic Nuclei Research, LASER 2004, held in Poznan, Poland, May 29-June 01, 2006 Researchers and PhD students interested in recent results in the nuclear structure investigation by laser spectroscopy, the progress of the experimental technique and the future developments in the field will find this volume indispensable. Reprinted from Hyperfine Interactions (HYPE) Volume ???

  5. International Oil Price’s Impacts on Carbon Emission in China’s Transportation Industry

    Directory of Open Access Journals (Sweden)

    Guoxing Zhang

    2014-09-01

    Full Text Available 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, the paper also analyses the impact mechanism of international oil price on the industrial carbon emission, and finally the paper uses the partial least squares regression model to study international oil price’s impact on carbon emissions in China’s transportation industry. With the independent variables’ historical data from 1994 to 2009 as a sample, the fitting of the industry carbon emissions is satisfying. And based on the data of 2011, the paper maintains the private car owning, passenger and freight transportation volume to study international oil prices’ impact on the industry carbon emissions at different levels of GDP.Findings: The results show that: with the same GDP growth, the industry carbon emissions increase with the rise in international oil prices, and vice versa, the industry carbon emissions decrease; and lastly when GDP increases to a certain extent, in both cases of international oil prices’ rise or fall, the industry carbon emissions will go up, and the industry carbon emissions increase even faster while the energy prices are rising.Practical implications: Limit the growth in private-vehicle ownership, change China's transport sector within the next short-term in the structure of energy consumption and put forward China's new energy, alternative energy sources and renewable energy application so as to weaken the dependence on international oil, and indirectly slowdown China's GDP growth rate, which are all possible

  6. Quantum test of the equivalence principle for atoms in coherent superposition of internal energy states

    Science.gov (United States)

    Rosi, G.; D'Amico, G.; Cacciapuoti, L.; Sorrentino, F.; Prevedelli, M.; Zych, M.; Brukner, Č.; Tino, G. M.

    2017-06-01

    The Einstein equivalence principle (EEP) has a central role in the understanding of gravity and space-time. In its weak form, or weak equivalence principle (WEP), it directly implies equivalence between inertial and gravitational mass. Verifying this principle in a regime where the relevant properties of the test body must be described by quantum theory has profound implications. Here we report on a novel WEP test for atoms: a Bragg atom interferometer in a gravity gradiometer configuration compares the free fall of rubidium atoms prepared in two hyperfine states and in their coherent superposition. The use of the superposition state allows testing genuine quantum aspects of EEP with no classical analogue, which have remained completely unexplored so far. In addition, we measure the Eötvös ratio of atoms in two hyperfine levels with relative uncertainty in the low 10-9, improving previous results by almost two orders of magnitude.

  7. Quantum test of the equivalence principle for atoms in coherent superposition of internal energy states.

    Science.gov (United States)

    Rosi, G; D'Amico, G; Cacciapuoti, L; Sorrentino, F; Prevedelli, M; Zych, M; Brukner, Č; Tino, G M

    2017-06-01

    The Einstein equivalence principle (EEP) has a central role in the understanding of gravity and space-time. In its weak form, or weak equivalence principle (WEP), it directly implies equivalence between inertial and gravitational mass. Verifying this principle in a regime where the relevant properties of the test body must be described by quantum theory has profound implications. Here we report on a novel WEP test for atoms: a Bragg atom interferometer in a gravity gradiometer configuration compares the free fall of rubidium atoms prepared in two hyperfine states and in their coherent superposition. The use of the superposition state allows testing genuine quantum aspects of EEP with no classical analogue, which have remained completely unexplored so far. In addition, we measure the Eötvös ratio of atoms in two hyperfine levels with relative uncertainty in the low 10-9, improving previous results by almost two orders of magnitude.

  8. Automated determination of the stable carbon isotopic composition (δ13C) of total dissolved inorganic carbon (DIC) and total nonpurgeable dissolved organic carbon (DOC) in aqueous samples: RSIL lab codes 1851 and 1852

    Science.gov (United States)

    Révész, Kinga M.; Doctor, Daniel H.

    2014-01-01

    The purposes of the Reston Stable Isotope Laboratory (RSIL) lab codes 1851 and 1852 are to determine the total carbon mass and the ratio of the stable isotopes of carbon (δ13C) for total dissolved inorganic carbon (DIC, lab code 1851) and total nonpurgeable dissolved organic carbon (DOC, lab code 1852) in aqueous samples. The analysis procedure is automated according to a method that utilizes a total carbon analyzer as a peripheral sample preparation device for analysis of carbon dioxide (CO2) gas by a continuous-flow isotope ratio mass spectrometer (CF-IRMS). The carbon analyzer produces CO2 and determines the carbon mass in parts per million (ppm) of DIC and DOC in each sample separately, and the CF-IRMS determines the carbon isotope ratio of the produced CO2. This configuration provides a fully automated analysis of total carbon mass and δ13C with no operator intervention, additional sample preparation, or other manual analysis. To determine the DIC, the carbon analyzer transfers a specified sample volume to a heated (70 °C) reaction vessel with a preprogrammed volume of 10% phosphoric acid (H3PO4), which allows the carbonate and bicarbonate species in the sample to dissociate to CO2. The CO2 from the reacted sample is subsequently purged with a flow of helium gas that sweeps the CO2 through an infrared CO2 detector and quantifies the CO2. The CO2 is then carried through a high-temperature (650 °C) scrubber reactor, a series of water traps, and ultimately to the inlet of the mass spectrometer. For the analysis of total dissolved organic carbon, the carbon analyzer performs a second step on the sample in the heated reaction vessel during which a preprogrammed volume of sodium persulfate (Na2S2O8) is added, and the hydroxyl radicals oxidize the organics to CO2. Samples containing 2 ppm to 30,000 ppm of carbon are analyzed. The precision of the carbon isotope analysis is within 0.3 per mill for DIC, and within 0.5 per mill for DOC.

  9. Erosion of Carbon-based spacecraft structures in LEO by Atomic Oxygen

    DEFF Research Database (Denmark)

    Jørgensen, John Leif

    1998-01-01

    Atomic oxygen is constantly generated on the topside of the atmosphere by ionizing radiation. The ionizing solar radiation, UV and particles, will on impact dissociate molecular oxygen to atomic oxygen. However, due to the ratio between the UV and the particle flux from the sun, and due to compar...

  10. Confined-interface-directed synthesis of Palladium single-atom catalysts on graphene/amorphous carbon

    DEFF Research Database (Denmark)

    Xi, Jiangbo; Sun, Hongyu; Zhang, Zheye

    2018-01-01

    The maximized atomic efficiency of supported catalysts is highly desired in heterogeneous catalysis. Therefore, the design and development of active, stable, and atomic metal-based catalysts remains a formidable challenge. To tackle these problems, it is necessary to investigate the interaction b...

  11. Comparative Study on Adsorption of Mn(II from Aqueous Solutions on Various Activated Carbons

    Directory of Open Access Journals (Sweden)

    K. A. Emmanuel

    2009-01-01

    Full Text Available The adsorption of Mn(II on indigenously prepared activated carbons (IPAC from Bombax malabaricum, Pithecelobium dulse, Ipomea batatas and Peltaforum ferraginium have been studied. The effects of various experimental parameters have been investigated using batch adsorption technique. The extent of Mn(II removal increased with decrease in initial concentration of the Mn(II, particle size of the adsorbent and increased with increase in contact time, amount of adsorbent used and the initial pH of the solution. Adsorption data were modeled using Freundlich and Langmuir adsorption isotherms and first order kinetic equations. The kinetics of adsorption was found to be first order with regard to intra-particle diffusion rate. The results indicate that such carbons could be employed as low cost adsorbents in waste water treatment for the removal of Mn(II.

  12. Adsorption of phenolic compounds from aqueous solutions using carbon nanoporous adsorbent coated with polymer

    Science.gov (United States)

    Anbia, Mansoor; Ghaffari, Arezoo

    2009-09-01

    Phenolic compounds are a widespread class of water pollutants that are known to cause serious human health problems; and the demand for effective adsorbents for the removal of toxic compounds is increasing. In this work adsorption of phenol, resorcinol and p-cresol on mesoporous carbon material (CMK-1) and modified with polyaniline polymer (CMK-1/PANI) has been investigated in attempt to explore the possibility of using nanoporous carbon as an efficient adsorbent for pollutants. It was found that CMK-1/PANI exhibits significant adsorption for phenolic derivatives. Batch adsorption studies were carried out to study the effect of various parameters like adsorbent dose, pH, initial concentration and contact time. From the sorption studies it was observed that the uptake of resorcinol was higher than other phenolic derivatives. Freundlich and Langmuir adsorption isotherms were used to model the equilibrium adsorption data for phenolic compounds.

  13. Clusters of interstitial carbon atoms near the graphite surface as a possible origin of dome-like features observed by STM

    OpenAIRE

    Elesin, V. F.; Openov, L. A.

    1999-01-01

    Formation of clusters of interstitial carbon atoms between the surface and second atomic layers of graphite is demonstrated by means of molecular dynamics simulations. It is shown that interstitial clusters result in the dome-like surface features that may be associated with some of the hillocks observed by STM on the irradiated graphite surface.

  14. High-performance magnetic carbon materials in dye removal from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Xiaoming, E-mail: dawn1026@163.com; Zhang, Yu; Dai, Yuan; Fu, Feng, E-mail: yadxfufeng@126.com

    2016-07-15

    To obtain a novel adsorbent with excellent adsorption capacity and convenient magnetic separation property, magnetic activated semi-coke was prepared by KOH activation method and further modified by FeCl{sub 3}. The surface morphology, physical structure, chemical properties and textural characteristics of unmodified semi-coke, KOH-modified semi-coke and magnetic activated semi-coke were characterized by scanning electron microscopy, X-ray powder diffraction, N{sub 2} adsorption-desorption measurement, and electronic differential system. The adsorption characteristics of the magnetic activated semi-coke were explored for the removal of methyl orang (MO), methylene blue (MB), congo red (CR), acid fuchsin (AF), and rhodamine B (RB) from aqueous solution. The effects of adsorption parameters, including adsorbent dosage, pH and contact time, were investigated by comparing the adsorption properties of the magnetic activated semi-coke to RB. The result showed that the magnetic activated semi-coke displayed excellent dispersion, convenient separation and high adsorption capacity. The adsorption experiment data indicated that the pseudosecond order model and the Langmuir model could well explain the adsorption processes of RB on the magnetic activated semi-coke, and the maximum adsorption capacity (q{sub m}) was 526.32 mg/g. The values of thermodynamic parameters (ΔG°, ΔH° and ΔS°) indicated that the adsorption process depended on the temperature of the aqueous phase, and it was spontaneous and exothermic in nature. As the addition of the magnetic activated semi-coke, the color of the solution significantly faded. Subsequently, fast aggregation of the magnetic activated semi-coke from their homogeneous dispersion in the presence of an external magnetic field could be happened. So, the magnetic activated semi-coke displayed excellent dispersion, convenient separation and high adsorption capacity. - Graphical abstract: As the addition of the magnetic activated semi

  15. The role of carbon chain length in the attachment between microbubbles and aqueous solutions of ionic liquid.

    Science.gov (United States)

    Chew, E K; Lee, K Y; Lau, E V

    2017-11-15

    The effects of varying carbon chain lengths (CCLs) and concentrations of aqueous solutions of imidazolium based ionic liquids on bubble particle attachment (BPA) will provide a better understanding in catering for the varying degrees of surface activities in the application of the flotation technology. The general trends of this study should also be applicable to homologous series of other cationic surfactants and ionic liquids. Zeta potentials of small air bubbles and bunker oil drops dispersed in aqueous solutions of n-methylimidazolium chloride ionic liquids (n=0, 2, 3, 6, 8, 10, 12) of concentrations ranging from 1000PPM to 8000PPM, as were interfacial tensions of these solutions with bunker oil (180cst) and contact angles made by air bubbles at interfaces between these solutions and thin layers of bunker oil on flat solid surfaces were investigated. Finally, interparticle forces analysis using the Derjaguin-Landau, Verwey-Overbeek (DLVO) theory is also included. Analysis using the DLVO theory showed attractive forces between the oil particles and micro-bubbles are significantly more prevalent in short CCLs solutions of imidazolium-based ILs in low concentrations, namely [C0mim][Cl] and [C2mim][Cl] at a maximum zeta potential difference of 75.3mV. The results from CA measurements follows similarly whereby low concentrations of ILs with short CCLs were in favor for the bubble-particle attachment process with angles ranging between 93.95° for [C0mim][Cl] and 97.28° for [C2mim][Cl]. IFT which is important in reducing coalescence for the preferential BPA process to occur in flotation decreases with an increase of CCL and concentration of IL. Copyright © 2017 Elsevier Inc. All rights reserved.

  16. Development of internal reforming carbonate fuel cell stack technology

    Energy Technology Data Exchange (ETDEWEB)

    Farooque, M.

    1990-10-01

    Activities under this contract focused on the development of a coal-fueled carbonate fuel cell system design and the stack technology consistent with the system design. The overall contract effort was divided into three phases. The first phase, completed in January 1988, provided carbonate fuel cell component scale-up from the 1ft{sup 2} size to the commercial 4ft{sup 2} size. The second phase of the program provided the coal-fueled carbonate fuel cell system (CGCFC) conceptual design and carried out initial research and development needs of the CGCFC system. The final phase of the program emphasized stack height scale-up and improvement of stack life. The results of the second and third phases are included in this report. Program activities under Phase 2 and 3 were designed to address several key development areas to prepare the carbonate fuel cell system, particularly the coal-fueled CFC power plant, for commercialization in late 1990's. The issues addressed include: Coal-Gas Related Considerations; Cell and Stack Technology Improvement; Carbonate Fuel Cell Stack Design Development; Stack Tests for Design Verification; Full-Size Stack Design; Test Facility Development; Carbonate Fuel Cell Stack Cost Assessment; and Coal-Fueled Carbonate Fuel Cell System Design. All the major program objectives in each of the topical areas were successfully achieved. This report is organized along the above-mentioned topical areas. Each topical area has been processed separately for inclusion on the data base.

  17. Carbon nanotubes randomly decorated with gold clusters: from nano{sup 2}hybrid atomic structures to gas sensing prototypes

    Energy Technology Data Exchange (ETDEWEB)

    Charlier, J-C; Zanolli, Z [Unite de Physico-Chimie et de Physique des Materiaux (PCPM), European Theoretical Spectroscopy Facility (ETSF), Universite Catholique de Louvain, Place Croix du Sud 1, B-1348 Louvain-la-Neuve (Belgium); Arnaud, L; Avilov, I V; Felten, A; Pireaux, J-J [Centre de Recherche en Physique de la Matiere et du Rayonnement (PMR-LISE), Facultes Universitaires Notre-Dame de la Paix, 61 Rue de Bruxelles, B-5000 Namur (Belgium); Delgado, M [Sensotran, s.l., Avenida Remolar 31, E-08820 El Prat de Llobregat, Barcelona (Spain); Demoisson, F; Reniers, F [Service de Chimie Analytique et Chimie des Interfaces (CHANI), Universite Libre de Bruxelles, Faculte des Sciences, CP255, Boulevard du Triomphe 2, B-1050 Bruxelles (Belgium); Espinosa, E H; Ionescu, R; Leghrib, R; Llobet, E [Department of Electronic Engineering, Universitat Rovira i Virgili, Avenida Paisos Catalans 26, E-43007 Tarragona (Spain); Ewels, C P; Suarez-Martinez, I [Institut des Materiaux Jean Rouxel (IMN), Universite de Nantes, 2 rue de la Houssiniere-BP 32229, F-44322 Nantes Cedex 3 (France); Guillot, J; Mansour, A; Migeon, H-N [Departement Science et Analyse des Materiaux, Centre de Recherche Public-Gabriel Lippmann, rue du Brill 41, L-4422 Belvaux (Luxembourg); Watson, G E, E-mail: jean-jacques.pireaux@fundp.ac.b [Vega Science Trust, Unit 118, Science Park SQ, Brighton, BN1 9SB (United Kingdom)

    2009-09-16

    Carbon nanotube surfaces, activated and randomly decorated with metal nanoclusters, have been studied in uniquely combined theoretical and experimental approaches as prototypes for molecular recognition. The key concept is to shape metallic clusters that donate or accept a fractional charge upon adsorption of a target molecule, and modify the electron transport in the nanotube. The present work focuses on a simple system, carbon nanotubes with gold clusters. The nature of the gold-nanotube interaction is studied using first-principles techniques. The numerical simulations predict the binding and diffusion energies of gold atoms at the tube surface, including realistic atomic models for defects potentially present at the nanotube surface. The atomic structure of the gold nanoclusters and their effect on the intrinsic electronic quantum transport properties of the nanotube are also predicted. Experimentally, multi-wall CNTs are decorated with gold clusters using (1) vacuum evaporation, after activation with an RF oxygen plasma and (2) colloid solution injected into an RF atmospheric plasma; the hybrid systems are accurately characterized using XPS and TEM techniques. The response of gas sensors based on these nano{sup 2}hybrids is quantified for the detection of toxic species like NO{sub 2}, CO, C{sub 2}H{sub 5}OH and C{sub 2}H{sub 4}.

  18. Carbon nanotubes randomly decorated with gold clusters: from nano2hybrid atomic structures to gas sensing prototypes.

    Science.gov (United States)

    Charlier, J-C; Arnaud, L; Avilov, I V; Delgado, M; Demoisson, F; Espinosa, E H; Ewels, C P; Felten, A; Guillot, J; Ionescu, R; Leghrib, R; Llobet, E; Mansour, A; Migeon, H-N; Pireaux, J-J; Reniers, F; Suarez-Martinez, I; Watson, G E; Zanolli, Z

    2009-09-16

    Carbon nanotube surfaces, activated and randomly decorated with metal nanoclusters, have been studied in uniquely combined theoretical and experimental approaches as prototypes for molecular recognition. The key concept is to shape metallic clusters that donate or accept a fractional charge upon adsorption of a target molecule, and modify the electron transport in the nanotube. The present work focuses on a simple system, carbon nanotubes with gold clusters. The nature of the gold-nanotube interaction is studied using first-principles techniques. The numerical simulations predict the binding and diffusion energies of gold atoms at the tube surface, including realistic atomic models for defects potentially present at the nanotube surface. The atomic structure of the gold nanoclusters and their effect on the intrinsic electronic quantum transport properties of the nanotube are also predicted. Experimentally, multi-wall CNTs are decorated with gold clusters using (1) vacuum evaporation, after activation with an RF oxygen plasma and (2) colloid solution injected into an RF atmospheric plasma; the hybrid systems are accurately characterized using XPS and TEM techniques. The response of gas sensors based on these nano(2)hybrids is quantified for the detection of toxic species like NO(2), CO, C(2)H(5)OH and C(2)H(4).

  19. Rational Design of Single Molybdenum Atoms Anchored on N-Doped Carbon for Effective Hydrogen Evolution Reaction.

    Science.gov (United States)

    Chen, Wenxing; Pei, Jiajing; He, Chun-Ting; Wan, Jiawei; Ren, Hanlin; Zhu, Youqi; Wang, Yu; Dong, Juncai; Tian, Shubo; Cheong, Weng-Chon; Lu, Siqi; Zheng, Lirong; Zheng, Xusheng; Yan, Wensheng; Zhuang, Zhongbin; Chen, Chen; Peng, Qing; Wang, Dingsheng; Li, Yadong

    2017-12-11

    The highly efficient electrochemical hydrogen evolution reaction (HER) provides a promising pathway to resolve energy and environment problems. An electrocatalyst was designed with single Mo atoms (Mo-SAs) supported on N-doped carbon having outstanding HER performance. The structure of the catalyst was probed by aberration-corrected scanning transmission electron microscopy (AC-STEM) and X-ray absorption fine structure (XAFS) spectroscopy, indicating the formation of Mo-SAs anchored with one nitrogen atom and two carbon atoms (Mo 1 N 1 C 2 ). Importantly, the Mo 1 N 1 C 2 catalyst displayed much more excellent activity compared with Mo 2 C and MoN, and better stability than commercial Pt/C. Density functional theory (DFT) calculation revealed that the unique structure of Mo 1 N 1 C 2 moiety played a crucial effect to improve the HER performance. This work opens up new opportunities for the preparation and application of highly active and stable Mo-based HER catalysts. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Carbon tetrachloride induced kidney and lung tissue damages and antioxidant activities of the aqueous rhizome extract of Podophyllum hexandrum

    Directory of Open Access Journals (Sweden)

    Zargar Bilal

    2011-02-01

    Full Text Available Abstract Background The present study was conducted to evaluate the in vitro and in vivo antioxidant properties of aqueous extract of Podophyllum hexandrum. The antioxidant potential of the plant extract under in vitro situations was evaluated by using two separate methods, inhibition of superoxide radical and hydrogen peroxide radical. Carbon tetrachloride (CCl4 is a well known toxicant and exposure to this chemical is known to induce oxidative stress and causes tissue damage by the formation of free radicals. Methods 36 albino rats were divided into six groups of 6 animals each, all animals were allowed food and water ad libitum. Group I (control was given olive oil, while the rest groups were injected intraperitoneally with a single dose of CCl4 (1 ml/kg as a 50% (v/v solution in olive oil. Group II received CCl4 only. Group III animals received vitamin E at a concentration of 50 mg/kg body weight and animals of groups IV, V and VI were given extract of Podophyllum hexandrum at concentration dose of 20, 30 and 50 mg/kg body weight. Antioxidant status in both kidney and lung tissues were estimated by determining the activities of antioxidative enzymes, glutathione reductase (GR, glutathione peroxidase (GPX, glutathione-S-transferase (GST and superoxide dismutase (SOD; as well as by determining the levels of reduced glutathione (GSH and thiobarbituric acid reactive substances (TBARS. In addition, superoxide and hydrogen peroxide radical scavenging activity of the extract was also determined. Results Results showed that the extract possessed strong superoxide and hydrogen peroxide radical scavenging activity comparable to that of known antioxidant butylated hydroxy toluene (BHT. Our results also showed that CCl4 caused a marked increase in TBARS levels whereas GSH, SOD, GR, GPX and GST levels were decreased in kidney and lung tissue homogenates of CCl4 treated rats. Aqueous extract of Podophyllum hexandrum successfully prevented the alterations

  1. Low-temperature aqueous-phase methanol dehydrogenation to hydrogen and carbon dioxide.

    Science.gov (United States)

    Nielsen, Martin; Alberico, Elisabetta; Baumann, Wolfgang; Drexler, Hans-Joachim; Junge, Henrik; Gladiali, Serafino; Beller, Matthias

    2013-03-07

    Hydrogen produced from renewable resources is a promising potential source of clean energy. With the help of low-temperature proton-exchange membrane fuel cells, molecular hydrogen can be converted efficiently to produce electricity. The implementation of sustainable hydrogen production and subsequent hydrogen conversion to energy is called "hydrogen economy". Unfortunately, its physical properties make the transport and handling of hydrogen gas difficult. To overcome this, methanol can be used as a material for the storage of hydrogen, because it is a liquid at room temperature and contains 12.6 per cent hydrogen. However, the state-of-the-art method for the production of hydrogen from methanol (methanol reforming) is conducted at high temperatures (over 200 degrees Celsius) and high pressures (25-50 bar), which limits its potential applications. Here we describe an efficient low-temperature aqueous-phase methanol dehydrogenation process, which is facilitated by ruthenium complexes. Hydrogen generation by this method proceeds at 65-95 degrees Celsius and ambient pressure with excellent catalyst turnover frequencies (4,700 per hour) and turnover numbers (exceeding 350,000). This would make the delivery of hydrogen on mobile devices--and hence the use of methanol as a practical hydrogen carrier--feasible.

  2. Carbon Fiber Manufacturing Facility Siting and Policy Considerations: International Comparison

    Energy Technology Data Exchange (ETDEWEB)

    Cook, Jeffrey J. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Booth, Samuel [National Renewable Energy Lab. (NREL), Golden, CO (United States)

    2017-06-21

    Carbon fiber is increasingly used in a wide variety of applications due largely to its superior material properties such as high strength-to-weight ratio. The current global carbon fiber manufacturing industry is predominately located in China, Europe, Japan, and the United States. The carbon fiber market is expected to expand significantly through 2024 and to require additional manufacturing capacity to meet demand. Carbon fiber manufacturing facilities can offer significant economic development and employment opportunities as exemplified by the $1 billion investment and 500 jobs expected at a new Toray plant in Moore, South Carolina. Though the market is expected to expand, it is unclear where new manufacturing facilities will locate to meet demand. This uncertainty stems from the lack of research evaluating how different nations with significant carbon fiber manufacturing capacity compare as it relates to certain manufacturing facility siting factors such as costs of labor and energy as well as policy directed at supporting carbon fiber development, domestic deployment, and exports. This report fills these gaps by evaluating the top carbon fiber manufacturing countries, including China, European Union countries, Japan, Mexico, South Korea, Taiwan, and the United States. The report documents how the United States compares to these countries based on a range of manufacturing siting considerations and existing policies related to carbon fiber. It concludes with a discussion of various policy options the United States could adopt to both (1) increase the competitiveness of the United States as it relates to attracting new carbon fiber manufacturing and (2) foster broader end-use markets for deployment.

  3. Carbon-modified electrode for ultra trace determination of Cd (II) in aqueous solution

    Science.gov (United States)

    Almustapha, Sakinatu; Khan, Aamir Amanat Ali; Omar, Abdul Aziz; Ariwahjoedi, Bambang; Abdullah, Mohd Azmuddin

    2014-10-01

    Increasing contamination of water by trace levels of heavy metals has become major environmental threats leading to an increased demand for the detection and monitoring of metal contaminants. In this work, modification of carbon electrode for Cd2+ detection using square wave anodic stripping voltammetry was reported. The deposition potential of -1.0 V in 0.1M acetate buffer for 240 sec, followed by square wave potential scan from -1.0 to -0.2 V were used. Stripping voltammogram showed current peaks corresponding to Cd2+. The sensitivity and selectivity of the modified electrodes for Cd2+ were also determined.

  4. Kinetic study of a Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation

    DEFF Research Database (Denmark)

    Bonalumi, Davide; Lillia, Stefano; Valenti, Gianluca

    2017-01-01

    This paper focuses on carbon capture in an Ultra Super Critical power plant. The technology selected for CO2 capture is based on cooled ammonia scrubbing in post-combustion mode, as recently investigated by the authors in another work. Here, a rate-based approach is adopted. In detail, a specific...... primary energy consumption for CO2 avoided (SPECCA) of 2.77 MJ/kgCO2 is calculated in case of 85% of CO2 capture, with an ultimate power plant efficiency of 37.27%....

  5. International Assessment of Carbon Nanotube Manufacturing and Applications

    National Research Council Canada - National Science Library

    Eklund, Peter; Ajayan, Pulickel; Blackmon, Robert; Hart, A. J; Kong, Jing; Pradhan, Bhabendra; Rao, Apparao; Rinzler, Andrew

    2007-01-01

    This WTEC study focuses on the manufacturing and applications of carbon nanotubes "CNTs" to identify recent progress in understanding the commercial potential of CNTs as viewed by academic, industrial...

  6. One-pot synthesis and control of aqueous soluble and organic soluble carbon dots from a designable waterborne polyurethane emulsion

    Science.gov (United States)

    Gu, Jiangjiang; Hu, Donghua; Huang, Jin; Huang, Xin; Zhang, Qiuhong; Jia, Xudong; Xi, Kai

    2016-02-01

    Carbon dots (CDs) have a wide range of applications and have drawn great interest in the recent decade. The fabrication and control of CDs with different solubilities are still urgent problems for their practical use. In this paper, aqueous soluble and organic soluble CDs (ACDs, OCDs) were produced by one-pot hydrothermal treatment of a designable waterborne polyurethane (WPU) emulsion. The difference in the solubility and fluorescence of these two kinds of CDs was attributed to the various functional groups on the surface, which were derived from the different segment fragments formed by hydrothermal treatment of a block polymer. It was found that the yields of the ACDs and OCDs could be regulated by means of selecting different soft segments in WPU. The more hydrophobic soft segments could result in an increase of the OCDs and a decrease of the ACDs. While the soft segments were hydrophilic or hydrolysable under hydrothermal conditions, only ACDs were obtained. The ACDs had good fluorescence and showed low cytotoxicity for use in multicolour bio-imaging. The OCDs processed good solubility in a wide range of organic solvents and were suitable for preparing fluorescent composite films with polymers.Carbon dots (CDs) have a wide range of applications and have drawn great interest in the recent decade. The fabrication and control of CDs with different solubilities are still urgent problems for their practical use. In this paper, aqueous soluble and organic soluble CDs (ACDs, OCDs) were produced by one-pot hydrothermal treatment of a designable waterborne polyurethane (WPU) emulsion. The difference in the solubility and fluorescence of these two kinds of CDs was attributed to the various functional groups on the surface, which were derived from the different segment fragments formed by hydrothermal treatment of a block polymer. It was found that the yields of the ACDs and OCDs could be regulated by means of selecting different soft segments in WPU. The more

  7. International Assessment of Carbon Nanotube Manufacturing and Applications

    Science.gov (United States)

    2007-06-01

    in Japan. Similarly, nanotubes (SWCNTs and MWCNTs) have been added to ceramic materials (e.g., alumina ) to enhance the fracture toughness of the...ICMR was built around Eklund’s work to mass- produce nanopowders produced by CO2 laser pyrolysis. ICMR moved to Silicon Valley two years later and...nanotube secondary battery using carbon nanotubes (Korea) • Method of synthesizing carbon nanotubes in the multistage bipolar alumina mould and

  8. Experiment and Optimization for Simultaneous Carbonation of Ca2+ and Mg2+ in A Two-phase System of Insoluble Diisobutylamine and Aqueous Solution

    Science.gov (United States)

    Wang, Wenlong; Wang, Man; Liu, Xin; Wang, Peng; Xi, Zhenqian

    2015-06-01

    An optimized approach of CO2 fixation in Ca2+/Mg2+-rich aqueous solutions using insoluble amine as an enhancing medium was reported. Apparent basicity was verified to be an effective indicator for the selection and optimization of organic amine systems and finally the diisobutylamine + n-octanol system was selected to enhance the carbonation reactions of CO2 in an artificial Ca2+/Mg2+-rich solution. In our experiments, when the volume ratio of insoluble organic phase to aqueous one was 2:1 and the reaction temperature was 28 °C, 92% of Ca2+ and 80% of Mg2+ could be converted to calcium and magnesium carbonate precipitates within 5 min of reaction with the bubbling-in of CO2. The organic amine system could be regenerated by using carbide slag as the regeneration agent and could still show attractive enhancement performances after 7 rounds of carbonation-regeneration experiments. In this way, the CO2 capture and sequestration was realized within one single process, with value-added Ca/Mg carbonates being the byproducts. In view of the vast availability of Ca2+/Mg2+-rich aqueous solutions and the feasible technical coordination with desalination industry, this novel process may have a good application potential in the future.

  9. The solar photospheric abundance of carbon : Analysis of atomic carbon lines with the CO5BOLD solar model

    NARCIS (Netherlands)

    Caffau, E.; Ludwig, H.-G.; Bonifacio, P.; Faraggiana, R.; Steffen, M.; Freytag, B.; Kamp, I.; Ayres, T. R.

    Context. The analysis of the solar spectra using hydrodynamical simulations, with a specific selection of lines, atomic data, and method for computing deviations from local thermodynamical equilibrium, has led to a downward revision of the solar metallicity, Z. We are using the latest simulations

  10. Adsorption of ciprofloxacin and norfloxacin from aqueous solution onto granular activated carbon in fixed bed column.

    Science.gov (United States)

    Darweesh, Teeba M; Ahmed, Muthanna J

    2017-04-01

    Carbonization of Phoenix dactylifera L stones followed by microwave K 2 CO 3 activation was adopted for preparation of granular activated carbon (KAC). High yield and favorable pore characteristics in terms of surface area and pore volume were reported for KAC as follows: 44%, 852m 2 /g, and 0.671cm 3 /g, respectively. The application of KAC as adsorbent for attraction of ciprofloxacin (CIP) and norfloxacin (NOR) was investigated using fixed bed systems. The effect of flow rate (0.5-1.5ml/min), bed height (15-25cm), and initial drug concentration (75-225mg/l) on the behavior of breakthrough curves was explained. The fixed bed analysis showed the better correlation of breakthrough data by both Thomas and Yoon-Nelson models. Inlet drug concentration was of greatest effect on breakthrough data compared to other fixed bed variables. Experimental and calculated breakthrough data were obtained for CIP and NOR adsorption on KAC, thus being important for design of fixed bed column. Copyright © 2016 Elsevier Inc. All rights reserved.

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

    Energy Technology Data Exchange (ETDEWEB)

    Devenney, Martin; Gilliam, Ryan; Seeker, Randy

    2014-06-01

    The objective of this project is to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA as well as flue gas from coal combustion. This topical report covers Phase 2b, which is the construction phase of pilot demonstration subsystems that make up the integrated plant. The subsystems included are the mineralization subsystem, the Alkalinity Based on Low Energy (ABLE) subsystem, the waste calcium oxide processing subsystem, and the fiber cement board production subsystem. The fully integrated plant is now capable of capturing CO2 from various sources (gas and coal) and mineralizing into a reactive calcium carbonate binder and subsequently producing commercial size (4ftx8ft) fiber cement boards. The topical report provides a description of the “as built” design of these subsystems and the results of the commissioning activities that have taken place to confirm operability. At the end of Phase 2b, the CCMP pilot demonstration is fully ready for testing.

  12. Green synthesis of biocompatible carbon dots using aqueous extract of Trapa bispinosa peel

    Energy Technology Data Exchange (ETDEWEB)

    Mewada, Ashmi; Pandey, Sunil, E-mail: gurus.spandey@gmail.com; Shinde, Sachin; Mishra, Neeraj; Oza, Goldie; Thakur, Mukeshchand; Sharon, Maheshwar; Sharon, Madhuri, E-mail: sharonmadhuri@gmail.com

    2013-07-01

    We are reporting highly economical plant based method for the production of luminescent water soluble carbon dots (C-dot) using Indian water plant Trapa bispinosa peel extract without adding any external oxidizing agent at 90 °C. C-dots ranging from 5 to 10 nm were found in the solution with a prominent green fluorescence under UV-light (λ{sub ex} = 365 nm). UV–vis spectra recorded at different time intervals (30–120 min) displayed signature absorption of C-dots between 400 and 600 nm. Fluorescence spectra of the dispersion after 120 min of synthesis exhibited characteristic emission peaks of C-dots when excited at 350, 400, 450 and 500 nm. C-dots were further analyzed using X-ray diffraction (XRD), Raman Spectroscopy and Thermo-Gravimetric Analysis (TGA). Structure of the C-dots was found to be turbostratic when studied using XRD. C-dots synthesized by our method were found to be exceptionally biocompatible against MDCK cells. Highlights: • Novel report on biosynthesis of water soluble carbon dots using plant source • Prominent green fluorescence under UV light • Highly biocompatible nanoparticles against MDCK cells • Excellent imaging properties under fluorescent light.

  13. Enhanced Adsorption of Selenium Ions from Aqueous Solution Using Iron Oxide Impregnated Carbon Nanotubes.

    Science.gov (United States)

    Bakather, Omer Y; Kayvani Fard, Ahmad; Ihsanullah; Khraisheh, Majeda; Nasser, Mustafa S; Atieh, Muataz Ali

    2017-01-01

    The aim of this research was to investigate the potential of raw and iron oxide impregnated carbon nanotubes (CNTs) as adsorbents for the removal of selenium (Se) ions from wastewater. The original and modified CNTs with different loadings of Fe2O3 nanoparticles were characterized using high resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), X-ray diffractometer (XRD), Brunauer, Emmett, and Teller (BET) surface area analyzer, thermogravimetric analysis (TGA), zeta potential, and energy dispersive X-ray spectroscopy (EDS). The adsorption parameters of the selenium ions from water using raw CNTs and iron oxide impregnated carbon nanotubes (CNT-Fe2O3) were optimized. Total removal of 1 ppm Se ions from water was achieved when 25 mg of CNTs impregnated with 20 wt.% of iron oxide nanoparticles is used. Freundlich and Langmuir isotherm models were used to study the nature of the adsorption process. Pseudo-first and pseudo-second-order models were employed to study the kinetics of selenium ions adsorption onto the surface of iron oxide impregnated CNTs. Maximum adsorption capacity of the Fe2O3 impregnated CNTs, predicted by Langmuir isotherm model, was found to be 111 mg/g. This new finding might revolutionize the adsorption treatment process and application by introducing a new type of nanoadsorbent that has super adsorption capacity towards Se ions.

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

    Energy Technology Data Exchange (ETDEWEB)

    Devenney, Martin; Gilliam, Ryan; Seeker, Randy

    2013-08-01

    The objective of this project is to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA. This topical report covers Subphase 2a which is the design phase of pilot demonstration subsystems. Materials of construction have been selected and proven in both lab scale and prototype testing to be acceptable for the reagent conditions of interest. The target application for the reactive carbonate material has been selected based upon small-scale feasibility studies and the design of a continuous fiber board production line has been completed. The electrochemical cell architecture and components have been selected based upon both lab scale and prototype testing. The appropriate quality control and diagnostic techniques have been developed and tested along with the required instrumentation and controls. Finally the demonstrate site infrastructure, NEPA categorical exclusion, and permitting is all ready for the construction and installation of the new units and upgrades.

  15. Novel Aluminum Oxide-Impregnated Carbon Nanotube Membrane for the Removal of Cadmium from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Ihsanullah

    2017-09-01

    Full Text Available An aluminum oxide-impregnated carbon nanotube (CNT-Al2O3 membrane was developed via a novel approach and used in the removal of toxic metal cadmium ions, Cd(II. The membrane did not require any binder to hold the carbon nanotubes (CNTs together. Instead, the Al2O3 particles impregnated on the surface of the CNTs were sintered together during heating at 1400 °C. Impregnated CNTs were characterized using XRD, while the CNT-Al2O3 membrane was characterized using scanning electron microscopy (SEM. Water flux, contact angle, and porosity measurements were performed on the membrane prior to the Cd(II ion removal experiment, which was conducted in a specially devised continuous filtration system. The results demonstrated the extreme hydrophilic behavior of the developed membrane, which yielded a high water flux through the membrane. The filtration system removed 84% of the Cd(II ions at pH 7 using CNT membrane with 10% Al2O3 loading. A maximum adsorption capacity of 54 mg/g was predicted by the Langmuir isotherm model for the CNT membrane with 10% Al2O3 loading. This high adsorption capacity indicated that adsorption was the main mechanism involved in the removal of Cd(II ions.

  16. Effectiveness of Quercus Branti Activated Carbon in Removal of Methylene Blue from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Abdolmotaleb Seidmohammadi

    2015-10-01

    Full Text Available Background & Aims of the Study: Dyes are one of the most contaminants in textile industrial wastewater that they are often carcinogenic, mutagenic and non-degradable. Therefore, with regard to environmental aspects, their removal from effluents is very essential. The purpose of this study was the perception of adsorption process and promotion of an economic technology for colored wastewater treatment. Therefore, activated carbon from Oak fruit bark was used as an effective and economic adsorbent. Materials & Methods: This study was performed at laboratory scale and batch system. At present study, the adsorbent surface properties was evaluated by use of the (FT-IR test and scanning electronic microscope (SEM. Also, effect of various operating parameters such as pH, contact time, adsorbent dose, initial dye concentration and temperature on dye removal from synthetic wastewater were studied. Results: In this study, maximum removal efficiency of methylene blue were achieved at optimal pH=6, reaction time 180 minutes, and adsorbent dose 2 gl-1. Methylene blue removal efficiency with initial concentration of 100 mg.l-1 was 91.08%. Conclusions: According to results, it was cleared that : Quercus branti activated carbon can be used as an effective and economic adsorbent in waste water treatment processes.

  17. Carbon Redistribution and Carbide Precipitation in a High-Strength Low-Carbon HSLA-115 Steel Studied on a Nanoscale by Atom Probe Tomography

    Science.gov (United States)

    Jain, Divya; Isheim, Dieter; Seidman, David N.

    2017-07-01

    HSLA-115 is a newly developed Cu-bearing high-strength low-carbon martensitic steel for use in Naval structural applications. This research provides, for the first time, a comprehensive compositional analysis of carbon redistribution and associated complex phase transformations in an isothermal aging study of HSLA-115 at 823 K (550 °C). Specifically, we characterize carbon segregation at lath boundaries, grain-refining niobium carbonitrides, cementite, and secondary hardening M2C carbides, in addition to copper precipitation, by 3D atom probe tomography (APT). Segregation of carbon (3 to 6 at. pct C) is observed at martensitic lath boundaries in the as-quenched and 0.12-hour aged microstructures. On further aging, carbon redistributes itself forming cementite and M2C carbides. Niobium carbonitride precipitates do not dissolve during the austenitizing treatment and are inherited in the as-quenched and aged microstructures; these are characterized along with cementite by synchrotron X-ray diffraction and APT. Sub-nanometer-sized M2C carbide precipitates are observed after the formation of Cu precipitates, co-located with the latter, indicating heterogeneous nucleation of M2C. The temporal evolution of the composition and morphology of M2C carbides at 823 K (550 °C) is described using APT; their precipitation kinetics is intertwined with Cu precipitates, affecting the bulk mechanical properties of HSLA-115. Phase compositions determined by APT are compared with computed compositions at thermodynamic equilibrium using ThermoCalc.

  18. Carbon Redistribution and Carbide Precipitation in a High-Strength Low-Carbon HSLA-115 Steel Studied on a Nanoscale by Atom Probe Tomography

    Energy Technology Data Exchange (ETDEWEB)

    Jain, Divya; Isheim, Dieter; Seidman, David N. (NWU)

    2017-05-09

    HSLA-115 is a newly developed Cu-bearing high-strength low-carbon martensitic steel for use in Naval structural applications. This research provides, for the first time, a comprehensive compositional analysis of carbon redistribution and associated complex phase transformations in an isothermal aging study of HSLA-115 at 823 K (550 °C). Specifically, we characterize carbon segregation at lath boundaries, grain-refining niobium carbonitrides, cementite, and secondary hardening M2C carbides, in addition to copper precipitation, by 3D atom probe tomography (APT). Segregation of carbon (3 to 6 at. pct C) is observed at martensitic lath boundaries in the as-quenched and 0.12-hour aged microstructures. On further aging, carbon redistributes itself forming cementite and M2C carbides. Niobium carbonitride precipitates do not dissolve during the austenitizing treatment and are inherited in the as-quenched and aged microstructures; these are characterized along with cementite by synchrotron X-ray diffraction and APT. Sub-nanometer-sized M2C carbide precipitates are observed after the formation of Cu precipitates, co-located with the latter, indicating heterogeneous nucleation of M2C. The temporal evolution of the composition and morphology of M2C carbides at 823 K (550 °C) is described using APT; their precipitation kinetics is intertwined with Cu precipitates, affecting the bulk mechanical properties of HSLA-115. Phase compositions determined by APT are compared with computed compositions at thermodynamic equilibrium using ThermoCalc.

  19. Improved electroless plating method through ultrasonic spray atomization for depositing silver nanoparticles on multi-walled carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Qi [School of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Xie, Ming [Kunming Institute of Precious Metals, Kunming 650106 (China); Liu, Yichun, E-mail: liuyichun@kmust.edu.cn [School of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Yi, Jianhong [School of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China)

    2017-07-01

    Highlights: • Electroless plating method assisted by ultrasonic spray atomization was developed. • This method leads to much more uniform silver coatings on MWCNTs. • The plating parameters affect the layer morphologies a lot. - Abstract: A novel method was developed to deposit nanosized silver particles on multi-walled carbon nanotubes (MWCNTs). The electroless plating of silver on MWCNTs accomplished in small solution drops generated by ultrasonic spray atomization, which inhibited excessive growth of silver particles and led to much more uniform nanometer grain-sized coatings. The results showed that pretreatment was essential for silver particles to deposit on the MWCNTs, and the electrolyte concentration and reaction temperature were important parameters which had a great influence on the morphology and structure of the silver coatings. Possible mechanisms of this method are also discussed in the paper.

  20. Mechanism of DNA cleavage by cationic manganese porphyrins: hydroxylations at the 1'-carbon and 5'-carbon atoms of deoxyriboses as initial damages.

    Science.gov (United States)

    Pratviel, G; Pitié, M; Bernadou, J; Meunier, B

    1991-11-25

    Cationic manganese-porphyrin complexes, free or targetted with an intercalating agent, are able to cleave DNA using oxygen atom donors like potassium monopersulfate or magnesium monoperphthalate as coreactants. Detailed studies of the cleavage of calf thymus DNA, before and after a heating step, show that free bases and 5-methylene-2-furanone are the main reaction products, indicating that hydroxylation at the 1'-carbon atom is the main target of these chemical agents. These data confirm that metalloporphyrin derivatives interact with the minor groove of double-stranded DNA. Hydroxylation of one of the two C-H bonds at position-5' is another initial DNA damage, characterized by the formation of furfural as sugar degradation product. Besides these two main initial damage sites, a low contribution of a hydroxylation reaction at C4' can not be definitively discounted, while an hydroperoxidation route at C4' can be excluded.

  1. Batch sorption dynamics and equilibrium for the removal of lead ions from aqueous phase using activated carbon developed from coffee residue activated with zinc chloride.

    Science.gov (United States)

    Boudrahem, F; Aissani-Benissad, F; Aït-Amar, H

    2009-07-01

    Lignocellulosic materials are good precursors for the production of activated carbon. In this work, coffee residue has been used as raw material in the preparation of powder activated carbon by the method of chemical activation with zinc chloride for the sorption of Pb(II) from dilute aqueous solutions. The influence of impregnation ratio (ZnCl2/coffee residue) on the physical and chemical properties of the prepared carbons was studied in order to optimize this parameter. The optimum experimental condition for preparing predominantly microporous activated carbons with high pore surface area (890 m2/g) and micropore volume (0.772 cm3/g) is an impregnation ratio of 100%. The developed activated carbon shows substantial capability to sorb lead(II) ions from aqueous solutions and for relative impregnation ratios of 75 and 100%, the maximum uptake is practically the same. Thus, 75% represents the optimal impregnation ratio. Batch experiments were conducted to study the effects of the main parameters such as contact time, initial concentration of Pb(II), solution pH, ionic strength and temperature. The maximum uptake of lead(II) at 25 degrees C was about 63 mg/g of adsorbent at pH 5.8, initial Pb(II) concentration of 10 mg/L, agitation speed of 200 rpm and ionic strength of 0.005 M. The kinetic data were fitted to the models of pseudo-first order and pseudo-second order, and follow closely the pseudo-second order model. Equilibrium sorption isotherms of Pb(II) were analyzed by the Langmuir, Freundlich and Temkin isotherm models. The Freundlich model gives a better fit than the others. Results from this study suggest that activated carbon produced from coffee residue is an effective adsorbent for the removal of lead from aqueous solutions and that ZnCl2 is a suitable activating agent for the preparation of high-porosity carbons.

  2. Equilibrium Solubility of CO2 in Aqueous Potassium Taurate Solutions : Part 1. Crystallization in Carbon Dioxide Loaded Aqueous Salt Solutions of Amino Acids

    NARCIS (Netherlands)

    Kumar, P.S.; Hogendoorn, J.A.; Feron, P.H.M.; Versteeg, G.F.

    2003-01-01

    Crystallization of a reaction product was observed during the absorption of CO2 in aqueous potassium taurate solutions at 298 K. The crystallizing solid was found to be the protonated amine. The critical CO2 loading value at which crystallization occurred was measured for various amino acid salt

  3. Effects of doping in 25-atom bimetallic nanocluster catalysts for carbon–carbon coupling reaction of iodoanisole and phenylacetylene

    Directory of Open Access Journals (Sweden)

    Zhimin Li

    2016-10-01

    Full Text Available We here report the catalytic effects of foreign atoms (Cu, Ag, and Pt doped into well-defined 25-gold-atom nanoclusters. Using the carbon-carbon coupling reaction of p-iodoanisole and phenylacetylene as a model reaction, the gold-based bimetallic MxAu25−x(SR18 (–SR=–SCH2CH2Ph nanoclusters (supported on titania were found to exhibit distinct effects on the conversion of p-iodoanisole as well as the selectivity for the Sonogashira cross-coupling product, 1-methoxy-4-(2-phenylethynylbenzene. Compared to Au25(SR18, the centrally doped Pt1Au24(SR18 causes a drop in catalytic activity but with the selectivity retained, while the AgxAu25−x(SR18 nanoclusters gave an overall performance comparable to Au25(SR18. Interestingly, CuxAu25−x(SR18 nanoclusters prefer the Ullmann homo-coupling pathway and give rise to product 4,4′-dimethoxy-1,1′-biphenyl, which is in opposite to the other three nanocluster catalysts. Our overall conclusion is that the conversion of p-iodoanisole is largely affected by the electronic effect in the bimetallic nanoclusters’ 13-atom core (i.e., Pt1Au12, CuxAu13−x, and Au13, with the exception of Ag doping, and that the selectivity is primarily determined by the type of atoms on the MxAu12−x shell (M=Ag, Cu, and Au in the nanocluster catalysts.

  4. Physics and Its Multiple Roles in the International Atomic Energy Agency

    Science.gov (United States)

    Massey, Charles D.

    2017-01-01

    The IAEA is the world's centre for cooperation in the nuclear field. It was set up as the world's ``Atoms for Peace'' organization in 1957 within the United Nations family. The Agency works with its Member States and multiple partners worldwide to promote the safe, secure and peaceful use of nuclear technologies. Three main areas of work underpin the IAEA's mission: Safety and Security, Science and Technology, and Safeguards and Verification. To carry out its mission, the Agency is authorized to encourage and assist research on, and development and practical application of, atomic energy for peaceful uses throughout the world; foster the exchange of scientific and technical information on peaceful uses of atomic energy; and encourage the exchange of training of scientists and experts in the field of peaceful uses of atomic energy. Nowadays, nuclear physics and nuclear technology are applied in a great variety of social areas, such as power production, medical diagnosis and therapies, environmental protection, security control, material tests, food processing, waste treatments, agriculture and artifacts analysis. This presentation will cover the role and practical application of physics at the IAEA, and, in particular, focus on the role physics has, and will play, in nuclear security.

  5. Adsorption isotherms of phenolic compounds from aqueous solutions onto activated carbon fibers

    Energy Technology Data Exchange (ETDEWEB)

    Juang, R.S. [Yuan-Ze Inst. of Tech., Taoyuan (Taiwan, Province of China). Dept. of Chemical Engineering; Wu, F.C.; Tseng, R.L. [Lien-Ho Junior Coll. of Technology, Miaoli (Taiwan, Province of China). Dept. of Chemical and Environmental Engineering

    1996-05-01

    Phenolic compounds exist widely in the industrial effluents such as those from oil refineries and the coal tar, plastics, leather, paint, pharmaceutical, and steel industries. Since they are highly toxic and are, in general, not amenable to biological degradation, methods of treatment are continuously being modified and developed. Liquid-phase adsorption equilibria of eight phenolic compounds onto activated carbon fibers were measured in the concentration range 40--500 g/m{sup 3} at 303 K. High adsorption capacities were observed for the chlorinated phenols compared to the methyl-substituted phenols. Several two- and three-parameter isotherm equations were tested. Among the equations tried, the three-parameter equation of Jossens et al. based on a heterogeneous surface adsorption theory was found to be the most satisfactory over the entire range of concentration. The widely used two-parameter equations of Langmuir and Freundlich were not applicable to the present adsorption systems.

  6. Contrast and phase-shift of a trapped atom interferometer using a thermal ensemble with internal state labelling

    Science.gov (United States)

    Dupont-Nivet, M.; Westbrook, C. I.; Schwartz, S.

    2016-11-01

    We report a theoretical study of a double-well Ramsey interferometer using internal state labelling. We consider the use of a thermal ensemble of cold atoms rather than a Bose-Einstein condensate to minimise the effects of atomic interactions. To maintain a satisfactory level of coherence in this case, a high degree of symmetry is required between the two arms of the interferometer. Assuming that the splitting and recombination processes are adiabatic, we theoretically derive the phase-shift and the contrast of such an interferometer in the presence of a gravity or an acceleration field. We also consider using a ‘shortcut to adiabaticity’ protocol to speed up the splitting process and discuss how such a procedure affects the phase shift and contrast. We find that the two procedures lead to phase-shifts of the same form.

  7. Adsorption of ibuprofen from aqueous solution on chemically surface-modified activated carbon cloths

    Directory of Open Access Journals (Sweden)

    Hanen Guedidi

    2017-05-01

    Full Text Available This study aims to investigate the performance of an activated carbon cloth for adsorption of ibuprofen. The cloth was oxidized by a NaOCl solution (0.13 mol L−1 or thermally treated under N2 (700 °C for 1 hour. The raw and modified cloths were characterized by N2 adsorption–desorption measurement at 77 K, CO2 adsorption at 273 K, Boehm titrations, pHPZC measurements, X-ray Photoelectron Spectroscopy analysis, and by infrared spectroscopy. The NaOCl treatment increases the acidic sites, mostly creating phenolic and carboxylic groups and decreases both the specific surface area and slightly the micropore volume. However, the thermal treatment at 700 °C under N2 induced a slight increase in the BET specific surface area and yielded to the only increase in the carbonyl group content. Ibuprofen adsorption studies of kinetics and isotherms were carried out at pH = 3 and 7. The adsorption properties were correlated to the cloth porous textures, surface chemistry and pH conditions. The isotherms of adsorption were better reproduced by Langmuir–Freundlich models at 298, 313 and 328 K. The adsorption of ibuprofen on the studied activated carbon cloths at pH 3 was an endothermic process. The pore size distributions of all studied ibuprofen-loaded fabrics were determined by DFT method to investigate the accessible porosity of the adsorbate. Both treatments do not influence the kind of micropores where the adsorption of ibuprofen occurred.

  8. Aromatization process of hydrocarbons containing 2 to 4 carbon atoms in the presence of alumino-silicate catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Alario, F.; Deves, J.M.

    1993-05-21

    The invention describes an aromatization process of hydrocarbons comprising 2 to 4 carbon atoms per molecule in the presence of a composite catalyst which contains: a MFI structure zeolite in the form hydrogen, containing in its structure Silicon, Aluminium and / or Gallium at least; a matrix; platinum metals at least and additive metal chosen among Stain, Germanium, Indium, Copper, Iron, Molybdenum, Gallium, Thallium, Gold, Silver, Ruthenium, Chrome, Tungsten and Lead at least; an halogen chosen among Fluorine, Chlorine, Bromine and Iodine at least; doping element chosen among Gallium and Zinc possibly and possibly alkaline or alkaline-earth metal.

  9. Aromatization process of hydrocarbons containing 2 to 4 carbon atoms in the presence of MFI structure zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Alario, F.; Deves, J.M.

    1993-05-21

    The invention describes an aromatization process of hydrocarbons comprising 2 to 4 carbon atoms per molecule in the presence of a composite catalyst which contains: a MFI structure zeolite containing an element chosen among alkaline or alkaline-earth metals, with a structure made of Silicon, Aluminium and / or Gallium; a matrix; platinum metals and additive metal chosen among Stain, Germanium, Indium, Copper, Iron, Molybdenum, Gallium, Thallium, Gold, Silver, Ruthenium, Chrome, Tungsten and Lead at least; an halogen chosen among Fluorine, Chlorine, Bromine and Iodine at least; Gallium and Zinc possibly; alkaline or alkaline-earth metal in the matrix preferentially. The invention describes also catalyst preparation and use for hydrocarbons aromatization reactions.

  10. Large-Scale Fabrication of Carbon Nanotube Probe Tips For Atomic Force Microscopy Critical Dimension Imaging Applications

    Science.gov (United States)

    Ye, Qi Laura; Cassell, Alan M.; Stevens, Ramsey M.; Meyyappan, Meyya; Li, Jun; Han, Jie; Liu, Hongbing; Chao, Gordon

    2004-01-01

    Carbon nanotube (CNT) probe tips for atomic force microscopy (AFM) offer several advantages over Si/Si3N4 probe tips, including improved resolution, shape, and mechanical properties. This viewgraph presentation discusses these advantages, and the drawbacks of existing methods for fabricating CNT probe tips for AFM. The presentation introduces a bottom up wafer scale fabrication method for CNT probe tips which integrates catalyst nanopatterning and nanomaterials synthesis with traditional silicon cantilever microfabrication technology. This method makes mass production of CNT AFM probe tips feasible, and can be applied to the fabrication of other nanodevices with CNT elements.

  11. Carbon 14 distribution in irradiated BWR fuel cladding and released carbon 14 after aqueous immersion of 6.5 years

    Energy Technology Data Exchange (ETDEWEB)

    Sakuragi, T. [Radioactive Waste Management Funding and Research Center, Tsukishima 1-15-7, Chuo City, Tokyo, 104-0052 (Japan); Yamashita, Y.; Akagi, M.; Takahashi, R. [TOSHIBA Corporation, Ukishima Cho 4-1, Kawasaki Ward, Kawasaki, 210-0862 (Japan)

    2016-07-01

    Spent fuel cladding which is highly activated and strongly contaminated is expected to be disposed of in an underground repository. A typical activation product in the activated metal waste is carbon 14 ({sup 14}C), which is mainly generated by the {sup 14}N(n,p){sup 14}C reaction and produces a significant exposure dose due to the large inventory, long half-life (5730 years), rapid release rate, and the speciation and consequent migration parameters. In the preliminary Japanese safety case, the release of radionuclides from the metal matrix is regarded as the corrosion-related congruent release, and the cladding oxide layer is regarded as a source of instant release fraction (IRF). In the present work, specific activity of {sup 14}C was measured using an irradiated BWR fuel cladding (Zircaloy-2, average rod burnup of 41.6 GWd/tU) which has an external oxide film having a thickness of 25.3 μm. The {sup 14}C specific activity of the base metal was 1.49*10{sup 4} Bq/g, which in the corresponding burnup is comparable to values in the existing literature, which were obtained from various irradiated claddings. Although the specific activity in oxide was 2.8 times the base metal activity due to the additive generation by the {sup 17}O(n,α){sup 14}C reaction, the {sup 14}C abundance in oxide was less than 10% of total inventory. A static leaching test using the cladding tube was carried out in an air-tight vessel filled with a deoxygenated dilute NaOH solution (pH of 12.5) at room temperature. After 6.5 years, {sup 14}C was found in each leachate fraction of gas phase and dissolved organics and inorganics, the total of which was less than 0.01% of the {sup 14}C inventory of the immersed cladding tube. A simple calculation based on the congruent release with Zircaloy corrosion has suggested that the 96.7% of released {sup 14}C was from the external oxide layer and 3.3% was from the base Zircaloy metal. However, both the {sup 14}C abundance and the low leaching rate

  12. Influence of carbon and metal oxide nanomaterials on aqueous concentrations of the munition constituents cyclotrimethylenetrinitramine (RDX) and tungsten.

    Science.gov (United States)

    Brame, Jonathon A; Kennedy, Alan J; Lounds, Christopher D; Bednar, Anthony J; Alvarez, Pedro J J; Scott, Andrea M; Stanley, Jacob K

    2014-05-01

    There is an increasing likelihood of interactions between nanomaterials and munitions constituents in the environment resulting from the use of nanomaterials as additives to energetic formulations and potential contact in waste streams from production facilities and runoff from training ranges. The purpose of the present research was to determine the ability of nano-aluminum oxide (Al(2)O(3)) and multiwalled carbon nanotubes (MWCNTs) to adsorb the munitions constituents cyclotrimethylenetrinitramine (RDX) and tungsten (W) from aqueous solution as a first step in determining the long-term exposure, transport, and bioavailability implications of such interactions. The results indicate significant adsorption of RDX by MWCNTs and of W by nano-Al(2)O(3) (but not between W and MWCNT or RDX and nano-Al(2)O(3)). Kinetic sorption and desorption investigations indicated that the most sorption occurs nearly instantaneously (nanomaterials following environmental release are likely. Time-dependent binding has implications for the bioavailability, migration, transport, and fate of munitions constituents in the environment. © 2014 SETAC.

  13. Enhanced decolorization of methyl orange in aqueous solution using iron-carbon micro-electrolysis activation of sodium persulfate.

    Science.gov (United States)

    Li, Peng; Liu, Zhipeng; Wang, Xuegang; Guo, Yadan; Wang, Lizhang

    2017-08-01

    Reactivity of sodium persulfate (PS) in the decolorization of methyl orange (MO) in aqueous solution using an iron-carbon micro-electrolysis (ICE) method was investigated. The effects of sodium persulfate doses, pH, Fe-to-C mass ratios, initial MO concentration as well as the reaction temperature were comprehensively studied in batch experiments. The ICE-PS coupled process was more suitable for wide ranges of pH, initial MO concentration and reaction temperature, accompanied by the reduction of Fe compared ICE. The MO removal efficiency improved substantially by ICE-PS technique, 76.03% for ICE and 91.27% for ICE-PS at experimental conditions of pH 3.0, Fe-to-C mass ratio 3:1, PS addition 10 mM and initial MO concentration 0.61 mM. Furthermore, the biodegradability index (BI) dramatically increased from 0.26 to 0.65. The binary hydroxyl and sulfate radicals that non-selectively degrade MO to the derivatives with small molecules are ascribed to ICE-PS method as detected by the UV-vis spectra. The PS activation resource was Fe2+ through the hydroxyl radical quenching reaction by the additive tert-butanol (TBA). This study provides an in-depth theoretical understanding of the development and wide commercial application of the ICE technology to refractory industrial dye wastewater treatment. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. Toxic metal removal from aqueous solution by advanced Carbon allotropes: a case study from the Sungun Copper Mine

    Directory of Open Access Journals (Sweden)

    Esmaeil Rahimi

    2017-04-01

    Full Text Available The sorption efficiencies of graphene oxide (GO and functionalized multi-walled carbon nanotubes (f-MWCNTs were investigated and elucidated to study their potential in treating acid mine drainage (AMD containing Cu2+, Mn2+, Zn2+, Pb2+, Fe3+ and Cd2+ metal ions. Several layered GO nanosheets and f-MWCNTs were formed via the modified Hummers’ method and the acid treatment of the MWCNTs, respectively. The prepared nanoadsorbents were characterized by field emission scanning electron microscopy (FE-SEM, Fourier transformed infrared (FTIR spectroscopy, and BET surface area analysis. The batch method was utilized to evaluate the pH effect, sorption kinetics and isotherms. The results demonstrated that the sorption capacities of the MWCNTs increased greatly after oxidation and those of the GO decreased after reduction. Hence, the sorption mechanisms seemed principally assignable to the chemical interactions between the metal ions and the surface functional groups of the adsorbents. Additionally, the adsorption isotherm results clearly depicted that the adsorption of the Cu2+ ion onto the GO adsorbent surface was well fitted and found to be in good agreement with the Langmuir isotherm model as the obtained regression constant value (R2 was found to be 0.9981. All results indicated that GO was a promising material for the removal of toxic metal ions from aqueous solutions in actual pollution management.

  15. Aqueous energy-storage cells based on activated carbon and LiMn2O4 electrodes

    Science.gov (United States)

    Hanna, Ortal; Luski, Shalom; Brousse, Thierry; Aurbach, Doron

    2017-06-01

    In recent years, there has been an increasing need for rechargeable energy-storage devices of many kinds. There are some applications for which energy density is important, whereas for others rate capability (high-power density) and prolonged durability are essential. Batteries address the need for high energy density, while electrochemical capacitors, so called, supercapacitors, can be relevant for the high power density purpose. In between these two kinds of devices, it is possible to develop hybrid systems which possess intermediate properties between supercapacitors and batteries, and which contain both a capacitive or pseudocapacitive electrode and a battery type electrode. With a good selection of electrodes, it is possible to achieve high-rate capability and durability, and also enhanced specific energy density compare to standard supercapacitors. This paper describes the development and study of Li-ion-based hybrid capacitor based on a carbon-based capacitive negative electrode, LiMn2O4 spinel as positive electrode and aqueous solutions with Li2SO4 salt as the electrolyte (pH = 7.5). Here, we demonstrate full hybrid devices as a proof of concept.

  16. Removal of sulfa drugs by sewage treatment in aqueous solution systems: activated carbon treatment and ozone oxidation.

    Science.gov (United States)

    Ogata, Fumihiko; Tominaga, Hisato; Kangawa, Moe; Inoue, Kenji; Kawasaki, Naohito

    2012-01-01

    This study investigates the activated carbon (AC) treatment and ozone oxidation of the sulfa drugs--sulfamethoxazole (SMX), sulfamonomethoxine (SMM), sulfadimidine (SDD), and sulfadimethoxine (SDM)--in aqueous solution systems. Three AC samples were prepared from Shirasagi (AC1 and AC2) and coal (AC3), and the surface functional groups, solution pH, specific surface areas, pore volumes, and morphologies of the three samples were evaluated. The specific surface areas were in the following order: AC1 (1391 m²/g) > AC2 (1053 m²/g) > AC3 (807 m²/g). The pore volume and mean pore diameter of AC3 were greater than those of AC1 and AC2. The concentration of sulfa drugs adsorbed onto the AC samples reached equilibrium within 150 h. Experimental data of the adsorption rate were fitted to a pseudo-second-order model. The amount of sulfa drugs adsorbed onto the AC samples was in the order of SDM Ozone was generated from oxygen gas using an A-27 ozone generator, and the complete degradation of the sulfa drugs by ozone treatment at 60 mL/min was achieved within 50 min. Ozone treatment caused the structure of the sulfa drugs to decompose via ozone oxidation.

  17. Study of Fluoride Affinity by Zirconium Impregnated Walnut Shell Carbon in Aqueous Phase: Kinetic and Isotherm Evaluation

    Directory of Open Access Journals (Sweden)

    M. Rajan

    2013-01-01

    Full Text Available This paper examines the kinetics of fluoride removal from water by the adsorbent zirconium-impregnated walnut-shell carbon (ZIWSC, exploring the mechanisms involved. The dependence of the adsorption of fluoride on the pH of the solution has been studied to achieve the optimum pH value and a better understanding of the adsorption mechanism. The presence of bicarbonate ions in aqueous solution was found to affect the fluoride removal indicating that these anions compete with the sorption of fluoride on adsorbents. The kinetic profile has been modeled using pseudo-first-order model, pseudo-second-order model, and intraparticle diffusion model. The kinetic sorption profiles offered excellent fit with pseudo-second-order model. Adsorption isotherms have been modeled by Langmuir, Freundlich, and Temkin equations, and their constants were determined. The equilibrium adsorption data were fitted reasonably well for Freundlich isotherm model. XRD and SEM patterns of the ZIWSC were recorded to get better insight into the mechanism of adsorption process.

  18. Modeling Kinetics of CO2 (Carbon Dioxide Mineral Sequestration in Heterogeneous Aqueous Suspensions Systems of Cement Dust

    Directory of Open Access Journals (Sweden)

    Henryk Świnder

    2013-01-01

    Full Text Available The necessity to reduce CO2 emission in the environment has encouraged people to search for solutions for its safe capture and storage. Known methods for carbon dioxide mineral sequestration are based primarily on the use of its binding reaction with metal oxides, mainly earth metals. Increasingly important, due to the availability and price, are processes based on the suspension of various wastes such as fly ash, cement dust or furnace slag. Due to the complexity of the mineral sequestration of CO2 in water-waste suspensions, an important issue is to determine the reaction mechanisms. This applies mainly to the initial period of the transformation phase of mineral wastes, and consequently with the occurrence of a number of transition states of ionic equilibria. The mechanisms and reaction rates in the various stages of the process of CO2 mineral sequestration in heterogeneous systems containing selected wastes are defined herein. This paper presents a method of modeling kinetics of this type of process, developed on the basis of the results of the absorption of CO2 thanks to the aqueous suspension of fly ash and cement dust. This allowed for the transfer of obtained experimental results into the mathematical formula, using the invariant function method, used to describe the processes.

  19. Protective effect of aqueous extracts from Rhizopus oryzae on liver injury induced by carbon tetrachloride in rats.

    Science.gov (United States)

    Suzuki, Takehito; Fukuoka, Hideo; Ushikoshi, Setsuo; Sato, Reiichiro; Morita, Hidetoshi; Takizawa, Tatsuya

    2015-05-01

    Hepatoprotective effects of Rhizopus oryzae/ U-1 aqueous extract (RU) were demonstrated in carbon tetrachloride (CCl4 )-induced liver-injured rats. In order to investigate the RU effects, the rats were administered RU at a dose of 10 or 100 mg/kg of body weight for 10 days before induction of the liver injury by oral administration of CCl4 (125 mg/kg body weight). (i) Pretreatment with RU caused a significant decrease in serum lactate dehydrogenase (LDH), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities that were increased by the administration of CCl4 . (ii) RU pretreatment (100 mg/kg) increased 5-bromo-2'-deoxyuridine incorporation at 48 h after CCl4 treatment in hepatocytes. (iii) Histological hematoxylin and eosin staining of the liver showed that RU pretreatment reduced the damage induced by CCl4 administration. (iv) Reverse transcriptase PCR analysis showed RU retreatment caused a transient but significant increase in hepatocyte growth factor (HGF) and a sustained and significant increase in insulin-like growth factor-I (IGF-I) gene expression in hepatocytes injured by CCl4 treatment. From these results, we conclude that oral pre-administration of RU was effective to suppress liver injury induced by the subsequent oral CCl4 administration, and RU-induced increase in IGF-I and HGF gene expression may be, even in part, involved in biological actions of RU in rats. © 2014 Japanese Society of Animal Science.

  20. Metaldehyde removal from aqueous solution by adsorption and ion exchange mechanisms onto activated carbon and polymeric sorbents.

    Science.gov (United States)

    Tao, Bing; Fletcher, Ashleigh J

    2013-01-15

    Metaldehyde removal from aqueous solution was evaluated using granular activated carbon (GAC), a non-functionalised hyper-cross-linked polymer Macronet (MN200) and an ion-exchange resin (S957) with sulfonic and phosphonic functional groups. Equilibrium experimental data were successfully described by Freundlich isotherm models. The maximum adsorption capacity of S957 (7.5 g metaldehyde/g S957) exceeded those of MN200 and GAC. Thermodynamic studies showed that sorption of metaldehyde onto all sorbents is endothermic and processes are controlled by entropic rather than enthalpic changes. Kinetic experiments demonstrated that experimental data for MN200 and GAC obey pseudo-second order models with rates limited by particle diffusion. Comparatively, S957 was shown to obey a pseudo-first order model with a rate-limiting step of metaldehyde diffusion through the solid/liquid interface. Results obtained suggest that metaldehyde adsorption onto MN200 and GAC are driven by hydrophobic interactions and hydrogen bonding, as leaching tendencies were high since no degradation of metaldehyde occurred. Conversely, adsorption of metaldehyde onto S957 occurs via ion-exchange processes, where sulfonic and phosphonic functionalities degrade adsorbed metaldehyde molecules and failure to detect metaldehyde in leaching studies for S957 supports this theory. Consequently, the high adsorption capacity and absence of leaching indicate S957 is promising for metaldehyde removal from source water. Copyright © 2012 Elsevier B.V. All rights reserved.

  1. Investigation of the interaction of carbon dioxide fluid with internal and external single-wall carbon nanotubes by DFT

    Directory of Open Access Journals (Sweden)

    M. Oftadeh

    2011-07-01

    Full Text Available The effective parameters of (5, 0 and (5, 5 single-wall carbon nanotubes during the interaction with carbon dioxide as sensors are determined. The interaction of carbon dioxide  molecules with internal and external walls of the nanotubes is studied using Gaussian 03 coding by density functional theory (DFT at the B3LYP/6-311G level of theory. CO2 rotation around tube axles vertically and parallel to the internal and external walls has been investigated. The carbon dioxide molecule is predicted to bind only weakly to nanotubes, and the tube-molecule interactions can be identified as physisorption. CO2 adsorption is stronger on external wallsthan on internal walls, and adsorption on the external wall of (5, 0 is stronger than on the external wall of (5, 5; the adsorption energies are exothermic and equal to -0.8884 and -0.0528 kcal/mol, respectively. The rotation energy barrier for (5, 5 is lower than that for (5, 0 in all rotations, therefore in these interactions (5, 5 is more active. The energy gap significantly changes in the presence of  carbon  dioxide molecules on the inside surface of (5, 0 and the electric conductivity is affected, but no remarkable change is observed in the electronic structure of (5, 5.

  2. Magnetic properties of a single iron atomic chain encapsulated in armchair carbon nanotubes: A Monte Carlo study

    Science.gov (United States)

    Masrour, R.; Jabar, A.; Hamedoun, M.; Benyoussef, A.; Hlil, E. K.

    2017-06-01

    The magnetic properties have been investigated of FeCuxC1-x for a Fe atom chain wrapped in armchair (N,N) carbon nanotubes (N = 4,6,8,10,12) diluted by Cu2+ ions using Monte Carlo simulations. The thermal total magnetization and magnetic susceptibility are found. The reduced transition temperatures of iron and carbon have been calculated for different N and the exchange interactions. The total magnetization is obtained for different exchange interactions and crystal field. The Magnetic hysteresis cycles are obtained for different N, the reduced temperatures and exchange interactions. The multiple magnetic hysteresis is found. This system shows it can be used as magnetic nanostructure possessing potential current and future applications in permanent magnetism, magnetic recording and spintronics.

  3. Attosecond angular flux of partial charges on the carbon atoms of benzene in non-aromatic excited state

    Science.gov (United States)

    Hermann, Gunter; Liu, ChunMei; Manz, Jörn; Paulus, Beate; Pohl, Vincent; Tremblay, Jean Christophe

    2017-09-01

    Recently, it was discovered that excitation of the oriented model benzene from its aromatic electronic ground state S0 (1A1g) to the non-aromatic S0 +S2 (1B1u) superposition state generates negative and positive partial charges on alternating carbon atoms. Subsequently, they vary periodically, due to adiabatic attosecond charge migration AACM. Here, we determine the angular electronic flux that mediates this new type of AACM, by means of quantum dynamics simulations. It is found to be periodic, with period τ bar = 590as , and with a pincer motion type pattern such that a total of 1.2 valence electrons flow concertedly between alternating sources and sinks at the carbon nuclei.

  4. Atomic force microscopy and electrochemical investigation on the corrosion behavior of carbon steel passivated by molybdate and chromate.

    Science.gov (United States)

    Chen, Zhenyu; Zhang, Xiulan; Huang, Ling; Guo, Xingpeng

    2013-02-01

    The effects of CrO(4)(2-) and MoO(4)(2-) ions on the corrosion behavior of carbon steel in 0.5 M NaCl solution have been studied using electrochemical measurements and atomic force microscopy. The results suggest that both ions have good inhibition effects on the general and pitting corrosion of carbon steel. At the same concentration, the inhibition efficiency of CrO(4)(2-) is higher than that of MoO(4)(2-). The passive film formed by CrO(4)(2-) is also much harder than that formed by MoO(4)(2-). The passive films formed by both ions are nonconductive. Copyright © 2012 Wiley Periodicals, Inc.

  5. Effects of acidified aqueous glycerol and glycerol carbonate pretreatment of rice husk on the enzymatic digestibility, structural characteristics, and bioethanol production.

    Science.gov (United States)

    Ebrahimi, Majid; Villaflores, Oliver B; Ordono, Emma E; Caparanga, Alvin R

    2017-03-01

    Rice husk as an abundant biomass was used in this study, and it contained 30.1% glucan and 13.5% xylan, 22.4% lignin. The pretreated rice husk with glycerol carbonate and acidified aqueous glycerol (10% water) at 90°C and 130°C for 60min had the maximum yield of glucan digestibility which was 78.2% and 69.7% respectively, using cellulase for 72h. The simultaneous saccharification and fermentation was conducted anaerobically at 37°C with Saccharomyces cerevisiae, 5% w/v glucan and 10FPU/g glucan of cellulase. 11.58 and 8.84g/L was the highest ethanol concentration after 3days of incubation form pretreated rice husk with glycerol carbonate and acidified aqueous glycerol respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

  6. Activated carbon prepared from coffee pulp: potential adsorbent of organic contaminants in aqueous solution.

    Science.gov (United States)

    Gonçalves, Maraisa; Guerreiro, Mário César; Ramos, Paulize Honorato; de Oliveira, Luiz Carlos Alves; Sapag, Karim

    2013-01-01

    The processing of coffee beans generates large amounts of solid and liquid residues. The solid residues (pulp, husk and parchment) represent a serious environmental problem and do not have an adequate disposal mechanism. In this work, activated carbons (ACs) for adsorption of organic compounds were prepared from coffee pulp by controlled temperature at different pulp/Na2HPO4 ratios (4:1, 2:1, 5:4 and 1:1). The N2 adsorption/desorption isotherms showed ACs with high quantities of mesopores and micropores and specific surface areas of 140, 150, 450 and 440 m(2)g(-1) for AC 4:1, AC 2:1, AC 5:4 and AC 1:1, respectively. The prepared material AC 5:4 showed a higher removal capacity of the organic contaminants methylene blue (MB), direct red (DR) and phenol than did a Merck AC. The maximum capacities for this AC are approximately 150, 120 and 120 mg g(-1) for MB, DR and phenol, respectively. Thus, a good adsorbent was obtained from coffee pulp, an abundant Brazilian residue.

  7. Removal of Cd 2+ ion from diluted aqueous solutions by electrodeposition on reticulated vitreous carbon electrodes

    Directory of Open Access Journals (Sweden)

    Tramontina Jucelânia

    2002-01-01

    Full Text Available The electrodeposition of Cd2+ ion was investigated in pH 4.8 sulfuric-sulfate solutions in the presence of dissolved O2. In potentiostatic conditions, using reticulated vitreous carbon (RVC electrodes of 30, 60 and 100 pores per inch (ppi, high removal efficiency values were achieved in the potential range from --0.90 to --1.10 V for solutions containing 5 and 10 mg L-1 of Cd2+ ion. In this potential range, Cd electrodeposition is a mass transport controlled reaction and the concentration of the metallic ion decays exponentially with time following a pseudo-first order kinetics. For the 30 ppi RVC, the current efficiency and removal efficiency values found were, respectively, 45 % and 96 % for a solution containing 10 mg L-1 of Cd2+ ion after 30 minutes electrolysis at --0.90 V while 33 % and 99% were found for the 60 ppi RVC. The concentration decay of Cd2+ ion in the solution was monitored after each experiment by anodic stripping voltammetry at a hanging mercury drop electrode.

  8. Equilibrium and kinetic studies on free cyanide adsorption from aqueous solution by activated carbon.

    Science.gov (United States)

    Behnamfard, Ali; Salarirad, Mohammad Mehdi

    2009-10-15

    Adsorption equilibrium and kinetics of free cyanide onto activated carbon were investigated in the batch tests, and the effects of contact time (1-72 h) and initial cyanide concentrations in the range of 102-532 mg/L were studied. Linear regression was used to determine the best fit of equilibrium and kinetics expressions. The two-parameter models including Freundlich, Dubinin-Radushkevich, Temkin and four different linearized forms of Langmuir and three-parameter models including Redlich-Peterson and Koble-Corrigan were employed for fitting the equilibrium data and it was found that, three-parameter models fitted the data better than the two-parameter models and among the three-parameter models the equilibrium data are best represented by Koble-Corrigan model. A number of kinetic models including fractional power, zero order, first order, pseudo-first order, Elovich, second order, intraparticle diffusion and four different linearized forms of pseudo-second order models were tested to fit the kinetic data. The latter was found to be consistent with the data. Intraparticle diffusion plots show that the adsorption process of free cyanide is a two steps process. In the first step, the adsorption of cyanide is fast while in the second step, cyanide adsorption slows down.

  9. Electrochemical reactivity of aqueous SO{sub 2} on glassy carbon electrodes in acidic media

    Energy Technology Data Exchange (ETDEWEB)

    Quijada, C. [Departamento de Ingenieria Textil y Papelera, EPSA, Universidad Politecnica de Valencia, Paseo del Viaducto 1, Alcoy, 03801 Alicante (Spain); Vazquez, J.L. [Departamento de Quimica Fisica, Universidad de Alicante, Ap. 99, 03080 Alicante (Spain)]. E-mail: jl.vazquez@ua.es

    2005-09-20

    The electrochemical reactivity of dissolved SO{sub 2} on glassy carbon (GC) electrodes was studied in sulfuric and perchloric acid solutions. The surface changes accompanying voltammetric scans were analysed with the aid of scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The influence of the GC pretreatment (polished versus electrochemically activated) on the oxidation of SO{sub 2} was examined. It was found that GC samples electrochemically treated so to develop a reduced graphite oxide film on the surface were more active for SO{sub 2} oxidation. The reduction of SO{sub 2} was observed to take place at potentials below 0.0 V to yield soluble sulfide species. This species was reoxidized on positive scans to form a sulfur deposit, consisting of an underlying layer of chemisorbed sulfur (161.9-162.3 eV) and an on-top layer of bulk elemental sulfur with S{sub 8}-like structure (163.6-163.8 eV). Surface sulfur did not impart electrocatalytic activity for the oxidation of SO{sub 2}.

  10. REMOVAL OF INDIGO CARMINE DYE (IC) BY BATCH ADSORPTION METHOD ONTO DRIED COLA NUT SHELLS AND ITS ACTIVE CARBON FROM AQUEOUS MEDIUM

    OpenAIRE

    Ankoro Naphtali Odogu*; Kouotou Daouda; Belibi Belibi Placide Desiré; Ndi Julius Nsami; Ketcha Joseph Mbadcam

    2016-01-01

    Natural cola nut shells and its active carbons were used to remove indigo carmine dye from aqueous solution using batch adsorption test. The effect of pH, contact time (t), adsorbent dose (m) and initial concentrations (Co) were investigated. The equilibrium adsorption data were analyzed by Langmuir, Freundlich, Tempkin and Dubin-Kaganer-Raduskushkevich classical isotherm models. This equilibrium data best fits with all the four isotherm models for cola nut shells. Langmuir and Freundlich equ...

  11. Anharmonicity of internal atomic oscillation and effective antineutrino mass evaluation from gaseous molecular tritium \\beta -decay

    CERN Document Server

    Lokhov, Alexey V

    2016-01-01

    Data analysis of the next generation effective antineutrino mass measurement experiment KATRIN requires reliable knowledge of systematic corrections. In particular, the width of the daughter molecular ion excitation spectrum rovibrational band should be known with a better then 1% precision. Very precise ab initio quantum calculations exist, and we compare them with the well known tritium molecule parameters within the framework of a phenomenological model. The rovibrational band width with accuracy of a few percent is interpreted as a result of the zero-point atomic oscillation in the harmonic potential. The Morse interatomic potential is used to investigate the impact of anharmonic atomic oscillations. The calculated corrections cannot account for the difference between the ab initio quantum calculations and the phenomenological model.

  12. ENAM'04 Fourth International Conference on Exotic Nuclei and Atomic Masses

    Energy Technology Data Exchange (ETDEWEB)

    Gross, C. J.; Nazarewicz, W.; Rykaczewski, K. P.

    2005-01-01

    The conference can trace its origins to the 1950s and 1960s with the Atomic Mass and Fundamental Constants (AMCO) and the Nuclei Far From Stability (NFFS) series of conferences. Held jointly in 1992, the conferences officially merged in 1995 and the fourth conference was held at Callaway Gardens in Pine Mountain, GA and was organized by the Physics Division at Oak Ridge National Laboratory. The conference covered a broad list of topics consisting of a series of invited and contributed presentation highlighting recent research in the following fields: Atomic masses, nuclear moments, and nuclear radii; Forms of radioactivity; Nuclear structure, nuclei at the drip lines, cluster phenomena; Reactions with radioactive ion beams; Nuclear astrophysics; Fundamental symmetries and interactions; Heaviest elements and fission; Radioactive ion beam production and experimental developments; Applications of exotic nuclei

  13. Atomic Scale Interface Manipulation, Structural Engineering, and Their Impact on Ultrathin Carbon Films in Controlling Wear, Friction, and Corrosion.

    Science.gov (United States)

    Dwivedi, Neeraj; Yeo, Reuben J; Yak, Leonard J K; Satyanarayana, Nalam; Dhand, Chetna; Bhat, Thirumaleshwara N; Zhang, Zheng; Tripathy, Sudhiranjan; Bhatia, Charanjit S

    2016-07-13

    Reducing friction, wear, and corrosion of diverse materials/devices using manipulation to engineer and control the friction, wear, corrosion, and structural characteristics of 0.7-1.7 nm carbon-based films on CoCrPt:oxide-based magnetic media. We demonstrate that when an atomically thin (∼0.5 nm) chromium nitride (CrNx) layer is sandwiched between the magnetic media and an ultrathin carbon overlayer (1.2 nm), it modifies the film-substrate interface, creates various types of interfacial bonding, increases the interfacial adhesion, and tunes the structure of carbon in terms of its sp(3) bonding. These contribute to its remarkable functional properties, such as stable and lowest coefficient of friction (∼0.15-0.2), highest wear resistance and better corrosion resistance despite being only ∼1.7 nm thick, surpassing those of ∼2.7 nm thick current commercial carbon overcoat (COC) and other overcoats in this work. While this approach has direct implications for advancing current magnetic storage technology with its ultralow thickness, it can also be applied to advance the protective and barrier capabilities of other ultrathin materials for associated technologies.

  14. FOREWORD: The 5th International Colloquium on Atomic Spectra and Oscillator Strengths for Astrophysical and Laboratory Plasmas

    Science.gov (United States)

    Tchang-Brillet, Wad Lydia; Wyart, Jean-François; Zeippen, Claude

    1996-01-01

    The 5th International Colloquium on Atomic Spectra and Oscillator Strengths for Astrophysical and Laboratory Plasmas was held in Meudon, France, from August 28 to 31 1995. It was the fifth in a series started by the Atomic Spectroscopic Group at the University of Lund, Sweden, in 1983. Then followed the meetings in Toledo, USA, Amsterdam, The Nether- lands and Gaithersburg, USA, with a three year period. The original title of the series ended with "... for Astrophysics and Fusion Research" and became more general with the 4th colloquium in Gaithersburg. The purpose of the present meeting was, in line with tradition, to bring together "producers" and "users" of atomic data so as to ensure optimal coordination. Atomic physicists who study the structure of atoms and their radiative and collisional properties were invited to explain the development of their work, emphasizing the possibilities of producing precise transition wavelengths and relative line intensities. Astrophysicists and laboratory plasma physicists were invited to review their present research interests and the context in which atomic data are needed. The number of participants was about 70 for the first three meetings, then exploded to 170 at Gaithersburg. About 140 participants, coming from 13 countries, attended the colloquium in Meudon. This large gathering was partly due to a number of participants from Eastern Europe larger than in the past, and it certainly showed a steady interest for interdisciplinary exchanges between different communities of scientists. This volume includes all the invited papers given at the conference and, in the appendix, practical information on access to some databases. All invited speakers presented their talks aiming at good communication between scientists from different backgrounds. A separate bound volume containing extended abstracts of the poster papers has been published by the Publications de l'Observatoire de Paris, (Meudon 1996), under the responsibility of

  15. The Role of Atomic Energy in the Promotion of International Collaboration

    Science.gov (United States)

    Rabi, I. I.

    1959-10-31

    A brief survey is presented of the international cooperation which made a success of the First Geneva Conference and which has initiated many international scientific meetings since that time. The policy of the United States in this respect is discussed. (J.S.R.)

  16. Atomic Structure and Energy Distribution of Collapsed Carbon Nanotubes of Different Chiralities

    Directory of Open Access Journals (Sweden)

    Julia A. Baimova

    2015-01-01

    Full Text Available For carbon nanotubes of sufficiently large diameter at sufficiently low temperature, due to the action of the van der Waals forces, the ground state is a bilayer graphene with closed edges, the so-called collapsed configuration. Molecular dynamics simulation of collapsed carbon nanotubes is performed. The effect of length, diameter, and chirality of the nanotubes on their properties is investigated. It is shown that collapsed nanotubes after relaxation have rippled structure which is strongly dependent on the nanotube chirality. The structural properties are studied by calculating the radial distribution function and energy distribution along various regions in the collapsed carbon nanotubes.

  17. Biofunctionalization of carbon nanotubes/chitosan hybrids on Ti implants by atom layer deposited ZnO nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Yizhou; Liu, Xiangmei [Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science & Engineering, Hubei University, Wuhan 430062 (China); Yeung, Kelvin W.K. [Division of Spine Surgery, Department of Orthopaedics & Traumatology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong (China); Chu, Paul K. [Department of Physics & Materials Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China); Wu, Shuilin, E-mail: shuilin.wu@gmail.com [Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science & Engineering, Hubei University, Wuhan 430062 (China)

    2017-04-01

    Highlights: • Carbon naonotubes/chitosan/ZnO coating was first constructed on Ti implants. • This system endowed Ti implants with excellent self-antibacterial activity. • The amount of Zn could be precisely controlled by atom layer deposition. • This system could regulate cell behaviors on metallic implants. - Abstract: One-dimensional (1D) nanostructures of ZnO using atomic layer deposition (ALD) on chitosan (CS) modified carbon nanotubes (CNTs) were first introduced onto the surfaces of biomedical implants. When the content of ZnO is not sufficient, CNTs can strengthen the antibacterial activity against E. coli and S. aureus by 8% and 39%, respectively. CS can improve the cytocompatibility of CNTs and ZnO. The amount of Zn content can be controlled by changing the cycling numbers of ALD processes. This hybrid coating can not only endow medical implants with high self-antibacterial efficacy against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) of over 73% and 98%, respectively, but also regulate the proliferation and osteogenic differentiation of osteoblasts by controlling the amount of ZnO.

  18. First-principles investigation of graphitic carbon nitride monolayer with embedded Fe atom

    Science.gov (United States)

    Abdullahi, Yusuf Zuntu; Yoon, Tiem Leong; Halim, Mohd Mahadi; Hashim, Md. Roslan; Lim, Thong Leng

    2018-01-01

    Density-functional theory (DFT) calculations with spin-polarized generalized gradient approximation and Hubbard U correction are carried out to investigate the mechanical, structural, electronic and magnetic properties of graphitic heptazine with embedded Fe atom under bi-axial tensile strain and applied perpendicular electric field. It was found that the binding energy of heptazine with embedded Fe atom system decreases as larger tensile strain is applied, while it increases as larger electric field strength is applied. Our calculations also predict a band gap at a peak value of 5% tensile strain but at expense of the structural stability of the system. The band gap open up at 5% tensile strain is due to distortion in the structure caused by the repulsive effect in the cavity between the lone pairs of the edge nitrogen atoms and dxy /dx2 -y2 orbital of Fe atom, forcing the unoccupied pz- orbital is forced to shift toward higher energy. The electronic and magnetic properties of the heptazine with embedded Fe system under perpendicular electric field up to a peak value of 8 V/nm is also well preserved despite an obvious buckled structure. Such properties are desirable for diluted magnetic semiconductors, spintronics, and sensing devices.

  19. Electrochemical atomic layer deposition of Pt nanostructures on carbon paper and Ni foam; poster

    CSIR Research Space (South Africa)

    Louw, EK

    2012-07-01

    Full Text Available The cost of the platinum catalyst hinders the progress of direct methanol fuel cells (DMFCs) into the commercial world. Electrochemical atomic layer deposition (ECALD) method was used to reduce the amount of Pt used and to increase its utilization...

  20. Vertical Alignment of Single-Walled Carbon Nanotubes on Nanostructure Fabricated by Atomic Force Microscope

    National Research Council Canada - National Science Library

    Lee, Haiwon

    2007-01-01

    This project focused on the behavior of single-wall carbon nanotubes (SWCNTs) in the electrophoresis cells and aligned growth of SWCNTs by thermal chemical vapor deposition on selectively deposited metallic nanoparticle...