WorldWideScience

Sample records for carbon 12 reactions

  1. Study of 16O(12C,α20Ne)α for the investigation of carbon-carbon fusion reaction via the Trojan Horse Method

    Science.gov (United States)

    Rapisarda, G. G.; Spitaleri, C.; Bordeanu, C.; Hons, Z.; Kiss, G. G.; La Cognata, M.; Mrazek, J.; Nita, C.; Pantelica, D.; Petrascu, H.; Pizzone, R. G.; Romano, S.; Szücs, T.; Trache, L.; Tumino, A.; Velisa, G.

    2016-04-01

    Carbon-carbon fusion reaction represents a nuclear process of great interest in astrophysics, since the carbon burning is connected with the third phase of massive stars (M > 8 M⊙) evolution. In spite of several experimental works, carbon-carbon cross section has been measured at energy still above the Gamow window moreover data at low energy present big uncertainty. In this paper we report the results about the study of the 16O(12C,α 20Ne)α reaction as a possible three-body process to investigate 12C(12C,α)20Ne at astrophysical energy via Trojan Horse Method (THM). This study represents the first step of a program of experiments aimed to measure the 12C+12C cross section at astrophysical energy using the THM.

  2. Measurement of fragment production DDX of 72 and 144 MeV 12C beam induced reaction on carbon using Bragg Curve Counter

    International Nuclear Information System (INIS)

    Double differential cross section (DDX) data of fragment production for 72 (6 MeV/nucleon) and 144 MeV (12 MeV/nucleon) 12C beam induced reaction on carbon were measured using a Bragg Curve Counter (BCC). The DDX data were obtained for fragments of He, Li, Be, B, C, N and O at 30 degree emission angle. Theoretical calculation using PHITS code with QMD+GEM model represents the DDX well except for components from reactions of direct process and α particle clustering process. (author)

  3. Effects of carbon source and carbon content on electrochemical performances of Li{sub 4}Ti{sub 5}O{sub 12}/C prepared by one-step solid-state reaction

    Energy Technology Data Exchange (ETDEWEB)

    Hu Xuebu [College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066 (China); Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, Sichuan 610041 (China); Lin Ziji [China National Quality Supervision and Inspection Center for Alcoholic Beverage Products and Processed Food, Luzhou, Sichuan 646100 (China); Yang Kerun [Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, Sichuan 610041 (China); Hua, Yongjian [China Aviation Lithium Battery Co. Ltd., Luoyang, Henan 471009 (China); Deng Zhenghua, E-mail: zhdeng@cioc.ac.cn [Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, Sichuan 610041 (China)

    2011-05-30

    Highlights: > A simple route to prepare the Li{sub 4}Ti{sub 5}O{sub 12}/C by one-step solid-state reaction. > Carbon source and carbon content are two important factors on the electrochemical performances of Li{sub 4}Ti{sub 5}O{sub 12}/C. > As-prepared Li{sub 4}Ti{sub 5}O{sub 12}/C under optimized conditions shows excellent electrochemical performances. - Abstract: Li{sub 4}Ti{sub 5}O{sub 12}/C composites were synthesized by one-step solid-state reaction method using four commonly used organic compounds or organic polymers as carbon source, i.e., polyacrylate acid (PAA), citric acid (CA), maleic acid (MA) and polyvinyl alcohol (PVA). The physical characteristics of Li{sub 4}Ti{sub 5}O{sub 12}/C composites were investigated by X-ray diffraction, electron microscopy, Raman spectroscopy, particle size distribution and thermogravimetry-derivative thermogravimetry techniques. Their electrochemical properties were characterized by cyclic voltammograms, electrochemical impedance spectra, constant current charge-discharge and rate charge-discharge. These analyses indicated that the carbon source and carbon content have a great effect on the physical and electrochemical performances of Li{sub 4}Ti{sub 5}O{sub 12}/C composites. An ideal carbon source and appropriate carbon content effectively improved the electrical contact between the Li{sub 4}Ti{sub 5}O{sub 12} particles, which enhanced the discharge capacity and rate capability of Li{sub 4}Ti{sub 5}O{sub 12}/C composites. PAA was the best carbon source for the synthesis of Li{sub 4}Ti{sub 5}O{sub 12}/C composites. When the carbon content was 3.49 wt.% (LiOH.H{sub 2}O/PAA molar ratio of 1), as-prepared Li{sub 4}Ti{sub 5}O{sub 12}/C showed the maximum discharge capacity. At 0.2 C, initial capacity of the optimized sample was 168.6 mAh g{sup -1} with capacity loss of 2.8% after 50 cycles. At 8 and 10 C, it showed discharge capacities of 143.5 and 132.7 mAh g{sup -1}, with capacity loss of 8.7 and 9.9% after 50 cycles

  4. Carbon Isotope Fractionation in Reactions of 1,2-Dibromoethane with FeS and Hydrogen Sulfide

    Science.gov (United States)

    EDB (1,2-dibromoethane) is frequently detected at sites impacted by leaded gasoline. In reducing environments, EDB is highly susceptible to abiotic degradation. A study was conducted to evaluate the potential of compound-specific isotope analysis (CSIA) in assessing abiotic degr...

  5. Cascade enzymatic reactions for efficient carbon sequestration.

    Science.gov (United States)

    Xia, Shunxiang; Zhao, Xueyan; Frigo-Vaz, Benjamin; Zheng, Wenyun; Kim, Jungbae; Wang, Ping

    2015-04-01

    Thermochemical processes developed for carbon capture and storage (CCS) offer high carbon capture capacities, but are generally hampered by low energy efficiency. Reversible cascade enzyme reactions are examined in this work for energy-efficient carbon sequestration. By integrating the reactions of two key enzymes of RTCA cycle, isocitrate dehydrogenase and aconitase, we demonstrate that intensified carbon capture can be realized through such cascade enzymatic reactions. Experiments show that enhanced thermodynamic driving force for carbon conversion can be attained via pH control under ambient conditions, and that the cascade reactions have the potential to capture 0.5 mol carbon at pH 6 for each mole of substrate applied. Overall it manifests that the carbon capture capacity of biocatalytic reactions, in addition to be energy efficient, can also be ultimately intensified to approach those realized with chemical absorbents such as MEA. PMID:25708541

  6. $^{12}$C nuclear reaction measurements for hadrontherapy.

    CERN Document Server

    B. Braunn, B; G. Ban, G; J.Colin, J; D. Cussol, D; J.M. Fontbonne, J M; F.R.. Lecolley, F R; C. Pautard, C; Haas, F; Lebhertz, D; Rousseau, M; Stuttge, L; Chevallier, M; Dauvergne, D; Le Foulher, F; Ray, C; Testa, E; Testa, M; Salsac, M D

    2010-01-01

    Hadrontherapy treatments require a very high precision on the dose deposition ( 2.5% and 1-2mm) in order to keep the benefits of the precise ions’ ballistic. The largest uncertainty on the physical dose deposition is due to ion fragmentation. Up to now, the simulation codes are not able to reproduce the fragmentation process with the required precision. To constraint the nuclear models and complete fragmentation cross sections databases; our collaboration has performed an experiment on May 2008 at GANIL with a 95 MeV/u 12C beam. We have measured the fluence, energy and angular distributions of charged fragments and neutrons coming from nuclear reactions of incident 12C on thick water-like PMMA targets. Preliminary comparisons between GEANT4 (G4BinaryLightIonReaction) simulations and experimental data show huge discrepancies.

  7. Fusion, resonances and scattering in 12C+12C reaction

    Indian Academy of Sciences (India)

    B Sahu; S K Agarwalla; C S Shastry

    2003-07-01

    The variation of fusion cross-section (fus) with energy in the 12C+12C collision is linked to the underlying resonance phenomenon through the behavior of reaction cross-section (r) of which fus is taken as a part. The calculation of fus is done through an energy-dependent imaginary potential in the optical model potential (OMP). Through dispersion relation, such an imaginary potential gives rise to energy-dependent real potential which is incorporated in the OMP. In our calculation, a form of potential for the nuclear part which has a soft repulsive in-built core is introduced based on similar works done earlier. The calculated results of fus are used to explain the oscillatory structure, astrophysical -factor and the decreasing trend at higher energies of the experimental fus data in the case of 12C+12C system with remarkable success. The potential used for fusion calculation is tested for fitting elastic scattering data at some energies and is found good in forward angles. Further improvement of the fitting of these data is obtained by incorporating a coupling potential in the surface region. About twenty resonances are observed in our calculation in the specific partial waves and some of them are found close to the experimentally identified resonances in 12C+12C reaction. Thus, we provide an integrated and comprehensive analysis of fusion, resonance and scattering data in the best studied case of 12C+12C reaction within the framework of optical potential model.

  8. Reactions on carbon anodes in aluminium electrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Eidet, Trygve

    1997-12-31

    The consumption of carbon anodes and energy in aluminium electrolysis is higher than what is required theoretically. This thesis studies the most important of the reactions that consume anode materials. These reactions are the electrochemical anode reaction and the airburn and carboxy reactions. The first part of the thesis deals with the kinetics and mechanism of the electrochemical anode reaction using electrochemical impedance spectroscopy. The second part deals with air and carboxy reactivity of carbon anodes and studies the effects of inorganic impurities on the reactivity of carbon anodes in the aluminium industry. Special attention is given to sulphur since its effect on the carbon gasification is not well understood. Sulphur is always present in anodes, and it is expected that the sulphur content of available anode cokes will increase in the future. It has also been suggested that sulphur poisons catalyzing impurities in the anodes. Other impurities that were investigated are iron, nickel and vanadium, which are common impurities in anodes which have been reported to catalyze carbon gasification. 88 refs., 92 figs., 24 tabs.

  9. Oxygen electrode reaction in molten carbonate fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Appleby, A.J.; White, R.E.

    1992-07-07

    Molten carbonate fuel cell system is a leading candidate for the utility power generation because of its high efficiency for fuel to AC power conversion, capability for an internal reforming, and a very low environmental impact. However, the performance of the molten carbonate fuel cell is limited by the oxygen reduction reaction and the cell life time is limited by the stability of the cathode material. An elucidation of oxygen reduction reaction in molten alkali carbonate is essential because overpotential losses in the molten carbonate fuel cell are considerably greater at the oxygen cathode than at the fuel anode. Oxygen reduction on a fully-immersed gold electrode in a lithium carbonate melt was investigated by electrochemical impedance spectroscopy and cyclic voltammetry to determine electrode kinetic and mass transfer parameters. The dependences of electrode kinetic and mass transfer parameters on gas composition and temperature were examined to determine the reaction orders and the activation energies. The results showed that oxygen reduction in a pure lithium carbonate melt occurs via the peroxide mechanism. A mass transfer parameter, D{sub O}{sup 1/2}C{sub O}, estimated by the cyclic voltammetry concurred with that calculated by the EIS technique. The temperature dependence of the exchange current density and the product D{sub O}{sup 1/2}C{sub O} were examined and the apparent activation energies were determined to be about 122 and 175 kJ/ mol, respectively.

  10. 12C+12C reactions at astrophysical energies: Tests of targets behaviour under beam bombardment

    International Nuclear Information System (INIS)

    12C(12C,α)20Ne and 12C(12C,p)23Na are the most important reactions during the carbon burning phase in stars. Direct measurements at the relevant astrophysical energy (E=1.5±0.3MeV) are very challenging because of the extremely small cross sections involved and of the high beam-induced background originating from impurities in the targets. In addition, persistent resonant structures at low energies are not well understood and make the extrapolation of the cross section from high energy data very uncertain. As a preliminary step towards the measurements of the 12C(12C,α)20Ne and 12C(12C,p)23Na reactions we intend to investigate the behaviour of targets under beam bombardment, specifically the quantitative measurement of hydrogen and deuterium content of highly pure stable carbon targets in relation to target temperature. Experiments are taking place at the CIRCE accelerator in Caserta, Italy and preliminary results are presented here

  11. Some Organic Reactions in Supercritical Carbon Dioxide

    Institute of Scientific and Technical Information of China (English)

    JIANG Huan-feng; YANG Xiao-yue; LI Guo-ping; ZOU Gang

    2004-01-01

    Organic reactions in supercritical carbon dioxide (scCO2) have facilitated great progress in recent years 1. ScCO2, as an environmentally friendly reaction medium, may be a substitute for volatile and toxic organic solvents and show some special advantages. Firstly, CO2 is inexpensive,nonflammable, nontoxic and chemical inert under many conditions. Secondly, scCO2 possesses hybrid properties of both liquid and gas, to the advantage of some reactions involving gaseous reagents. Control of the solvent density by variation of the temperature and pressure enables the solvent properties to be "tuned" to reactants. Finally, separating of CO2 from the reaction mixture is energy-efficient and simple. Here we disclose our new work on some organic reactions involving small molecules in scCO2.The results showed that the upper reactions in scCO2 could be carried out smoothly and thepressure of CO2 had a remarkable effect on the conversion and selectivity.

  12. 1,2 Migration in Carbenoid and Carbene Reactions

    Institute of Scientific and Technical Information of China (English)

    MA Ming; JIANG Nan; SHI Wei-Feng; WANG Jian-Bo

    2003-01-01

    @@ 1,2-Hydride, 1,2-alkyl and 1,2-aryl migrations are common in free carbene chemistry, and they are also fre quently encountered in the reactions of metal carbenes. In some cases, these migration reactions can compete with the typical reactions of metal carbenes, such as X-H (X = Si, C, O, N, S, etc. ) insertions and cyclopropanations. [1] The 1,2-migration also found synthetic application. An example is the SnCl2-promoted 1,2-hydride migration of α-diazo-β-hydroxy esters, known as Roskamp homologation, which leads to the formation of β-keto esters. [2

  13. Reaction from Dimethyl Carbonate to Diphenyl Carbonate. 1. Experimental Determination of the Chemical Equilibria

    NARCIS (Netherlands)

    Haubrock, J.; Raspe, M.; Versteeg, G.F.; Kooijman, H.A.; Taylor, R.; Hogendoorn, J.A.

    2008-01-01

    New experimental equilibrium data of the reaction of dimethyl carbonate (DMC) and phenol to methyl phenyl carbonate (MPC) and the subsequent disproportion and transesterification reaction of MPC to diphenyl carbonate (DPC) are presented and interpreted in terms of the reaction equilibrium coefficien

  14. Kinetic study of the reaction of uranium with various carbon-containing gases

    International Nuclear Information System (INIS)

    The kinetic study of the reaction U + CO2 and U + CO has been performed by a thermogravimetric method on a spherical uranium powder, in temperature ranges respectively from 460 to 690 deg. C and from 570 to 850 deg. C. The reaction with carbon dioxide leads to uranium dioxide. A carbon deposition takes place at the same time. The global reactions is the result of two reactions: U + 2 CO2 → UO2 + 2 CO U + CO2 → UO2 + C The reaction with carbon monoxide leads to a mixture of dioxide UO2, dicarbide UC2 and free carbon. The main reaction can be written. U + CO → 1/2 UO2 + 1/2 UC2 The free carbon results of the disproportionation of the carbon monoxide. A remarkable separation of the two phases UO2 and UC2 can be observed. A mechanism accounting for the phenomenon has been proposed. The two reactions U + CO2 and U + CO begin with a long germination period, after which, the reaction velocity seems to be limited in both cases by the ionic diffusion of oxygen through the uranium dioxide. (author)

  15. Carbon compounds in the atmosphere and their chemical reactions

    OpenAIRE

    Martišová, Petra

    2013-01-01

    The essay dissert on compounds of carbon in the atmosphere and its reaction. The most important are carbon dioxide, carbon monoxide and methane. Included among important compounds of carbon are volatile organic substances, polycyclic aromatic hydrocarbon and dioxin. Carbon dioxide and methane representing greenhouse gases have also indispensable meaning. As they, together with water vapour, nitrogen monoxide and other gases are causing the major part of greenhouse effect. Primarily because of...

  16. Carbon dioxide as a carbon source in organic transformation: carbon-carbon bond forming reactions by transition-metal catalysts.

    OpenAIRE

    Tsuji, Yasushi; Fujihara, Tetsuaki

    2012-01-01

    Recent carbon-carbon bond forming reactions of carbon dioxide with alkenes, alkynes, dienes, aryl zinc compounds, aryl boronic esters, aryl halides, and arenes having acidic C-H bonds are reviewed in which transition-metal catalysts play an important role.

  17. Reaction from Dimethyl Carbonate (DMC) to Diphenyl Carbonate (DPC). 2. Kinetics of the Reactions from DMC via Methyl Phenyl Carbonate to DPC

    NARCIS (Netherlands)

    Haubrock, J.; Wermink, W.; Versteeg, G.F.; Kooijman, H.A.; Taylor, R.; Sint Annaland, M. van; Hogendoorn, J.A.

    2008-01-01

    The kinetics of the reaction of dimethyl carbonate (DMC) and phenol to methyl phenyl carbonate (MPC) and the subsequent disproportion and transesterification reaction of methyl phenyl carbonate (MPC) to diphenyl carbonate (DPC) have been studied. Experiments were carried out in a closed batch reacto

  18. Carbon Isotopic Fractionation During Formation of Macromolecular Organic Grain Coatings via FTT Reactions

    Science.gov (United States)

    Nuth, J. A.; Johnson, N. M.; Elsila-Cook, J.; Kopstein, M.

    2011-01-01

    Observations of carbon isotopic fractionation of various organic compounds found in meteorites may provide useful diagnostic information concerning the environments and mechanisms that were responsible for their formation. Unfortunately, carbon has only two stable isotopes, making interpretation of such observations quite problematic. Chemical reactions can increase or decrease the C-13/C-12 ratio by various amounts, but the final ratio will depend on the total reaction pathway followed from the source carbon to the final product, a path not readily discernable after 4.5 billion years. In 1970 Libby showed that the C-13/C-12 ratios of terrestrial and meteoritic carbon were similar by comparing carbon from the Murchison meteorite to that of terrestrial sediments. More recent studies have shown that the C-13/C-12 ratio of the Earth and meteorites may be considerably enriched in C-13 compared to the ratio observed in the solar wind [2], possibly suggesting that carbon produced via ion-molecule reactions in cold dark clouds could be an important source of terrestrial and meteoritic carbon. However, meteoritic carbon has been subjected to parent body processing that could have resulted in significant changes to the C-13/C-12 ratio originally present while significant variation has been observed in the C-13/C-12 ratio of the same molecule extracted from different terrestrial sources. Again we must conclude that understanding the ratio found in meteorites may be difficult.

  19. Cluster correlation effects in 12C+12C and 14N+10B fusion-evaporation reactions

    Directory of Open Access Journals (Sweden)

    Morelli L.

    2015-01-01

    Full Text Available The decay of highly excited states of 24Mg is studied in fusion evaporation events completely detected in charge in the reactions 12C+12C and 14N+10B at 95 and 80 MeV incident energy respectively. The comparison of light charged particles measured spectra with statistical model predictions suggests that the dominant reaction mechanism is compound nucleus (CN formation and decay. However, in both reactions, a discrepancy with statistical expectations is found for α particles detected in coincidence with Carbon, Oxigen and Neon residues. The comparison between the two reactions shows that this discrepancy is only partly explained by an entrance channel effect. Evidence for cluster correlations in excited 24Mg CN is suggested by the comparison between the measured and calculated branching ratios for the channels involving α particles.

  20. Measurement of the ^12C+^12C Fusion Reaction with MUSIC

    Science.gov (United States)

    Carnelli, P. F. F.; Almaraz-Calderon, S.; Henderson, D.; Rehm, K. E.; Albers, M.; Alcorta, M.; Bertone, P. F.; Esbensen, H.; Fernandez-Niello, J. O.; Jiang, C. L.; Lighthall, J. C.; Marley, S. T.; Palchan-Hazan, T.; Pardo, R. C.; Paul, M.

    2012-10-01

    The fusion of the ^12C+^12C system is of great interest in nuclear structure and nuclear astrophysics. Above the Coulomb barrier, the excitation function of this system exhibits oscillations, which are not well understood. There is also a significant discrepancy between the experimental fusion cross-section and recent coupled-channel calculations that is not present in other carbon systems. To address these issues, we have re-measured the fusion excitation function for ^12,13C+^12C in the energy range of 10 MeV MUSIC) detector. The gas of the ionization chamber (CH4) served as both the target material and the counter gas. One of the main advantages of this method is that the excitation function is measured over a large range of energies using only one beam energy. This method has been proven to be successful and it will be used to measure fusion reactions in other light systems. The experimental results will be presented and compared to previous experimental data and theoretical models.

  1. Kinetic study of the reaction of uranium with various carbon-containing gases; Etude cinetique de la reaction sur l'uranium de differents gaz carbones

    Energy Technology Data Exchange (ETDEWEB)

    Feron, G. [Commissariat a l' Energie Atomique, Grenoble (France). Centre d' Etudes Nucleaires

    1963-09-15

    The kinetic study of the reaction U + CO{sub 2} and U + CO has been performed by a thermogravimetric method on a spherical uranium powder, in temperature ranges respectively from 460 to 690 deg. C and from 570 to 850 deg. C. The reaction with carbon dioxide leads to uranium dioxide. A carbon deposition takes place at the same time. The global reactions is the result of two reactions: U + 2 CO{sub 2} {yields} UO{sub 2} + 2 CO U + CO{sub 2} {yields} UO{sub 2} + C The reaction with carbon monoxide leads to a mixture of dioxide UO{sub 2}, dicarbide UC{sub 2} and free carbon. The main reaction can be written. U + CO {yields} 1/2 UO{sub 2} + 1/2 UC{sub 2} The free carbon results of the disproportionation of the carbon monoxide. A remarkable separation of the two phases UO{sub 2} and UC{sub 2} can be observed. A mechanism accounting for the phenomenon has been proposed. The two reactions U + CO{sub 2} and U + CO begin with a long germination period, after which, the reaction velocity seems to be limited in both cases by the ionic diffusion of oxygen through the uranium dioxide. (author) [French] L'etude cinetique des reactions U sol + CO{sub 2} gaz et U sol + CO gaz a ete effectuee par thermogravirnetrie sur une poudre d'uranium a grains spheriques, les domaines de temperature etudies s'etendant respectivement de 460 a 690 deg. C et de 570 a 850 deg. C. L'action du dioxyde de carbone conduit au dioxyde d'uranium UO{sub 2}; il se produit en meme temps un depot de carbone. La reaction globale resulte des deux reactions: U + 2 CO{sub 2} {yields} UO{sub 2} + 2 CO U + CO{sub 2} {yields} UO{sub 2} + C Le mono-oxyde de carbone conduit a un melange de dioxyde UO{sub 2}, de dicarbure UC{sub 2} et de carbone libre. La reaction principale s'ecrit: U + CO {yields} 1/2 UO{sub 2} + 1/2 UC{sub 2} Le carbone libre provient de la dismutation du mono-oxyde de carbone. On observe une separation remarquable des deux phases UO{sub 2} et UC{sub 2}; un mecanisme

  2. Friction stir processing on high carbon steel U12

    Energy Technology Data Exchange (ETDEWEB)

    Tarasov, S. Yu., E-mail: tsy@ispms.ru; Rubtsov, V. E., E-mail: rvy@ispms.ru [Institute of Strength Physics and Materials Science SB RAS, Tomsk, 634055 (Russian Federation); National Research Tomsk Polytechnic University, Tomsk, 634050 (Russian Federation); Melnikov, A. G., E-mail: melnikov-ag@tpu.ru [National Research Tomsk Polytechnic University, Tomsk, 634050 (Russian Federation)

    2015-10-27

    Friction stir processing (FSP) of high carbon steel (U12) samples has been carried out using a milling machine and tools made of cemented tungsten carbide. The FSP tool has been made in the shape of 5×5×1.5 mm. The microstructural characterization of obtained stir zone and heat affected zone has been carried out. Microhardness at the level of 700 MPa has been obtained in the stir zone with microstructure consisting of large grains and cementitte network. This high-level of microhardness is explained by bainitic reaction developing from decarburization of austenitic grains during cementite network formation.

  3. Friction stir processing on high carbon steel U12

    International Nuclear Information System (INIS)

    Friction stir processing (FSP) of high carbon steel (U12) samples has been carried out using a milling machine and tools made of cemented tungsten carbide. The FSP tool has been made in the shape of 5×5×1.5 mm. The microstructural characterization of obtained stir zone and heat affected zone has been carried out. Microhardness at the level of 700 MPa has been obtained in the stir zone with microstructure consisting of large grains and cementitte network. This high-level of microhardness is explained by bainitic reaction developing from decarburization of austenitic grains during cementite network formation

  4. Aminolysis Reaction of Glycerol Carbonate in Organic and Hydroorganic Medium

    OpenAIRE

    Nohra, Bassam; Candy, Laure; Blanco, Jean-François; Raoul, Yann; Mouloungui, Zephirin

    2012-01-01

    Aminolysis reaction of glycerol carbonate with primary amine in organic and hydroorganic media leads to the formation of two hydroxyurethane isomers and a partial decomposition of glycerol carbonate into glycerol. Aminolysis with a secondary amine promotes the condensation reaction and limits the formation of glycerol. The ratio of α versus β was determined by zgig 13C NMR. This technique permits computing the yield of α and β products in the medium. The quantity of glycerol was determined by...

  5. Combined reactions and separations using ionic liquids and carbon dioxide

    NARCIS (Netherlands)

    Kroon, M.C.

    2006-01-01

    A new and general type of process for the chemical industry is presented using ionic liquids and supercritical carbon dioxide as combined reaction and separation media. In this process, the carbon dioxide pressure controls the miscibility of reactants, products, catalyst and ionic liquid, enabling f

  6. Effect of Carbon Containing Materials on Pure Carbon Reaction-bonded SiC

    Institute of Scientific and Technical Information of China (English)

    JI Xiaoli; WEI Lei; SUN Feng

    2008-01-01

    Petroleum coke, graphite, gas carbon and lower sulfur carbon black were used to prepare reaction-bonded silicon carbide. The influences of different carbon containing materials on properties of carbonaceous precursors, sintering process, and microstructure of the prepared SiC were researched. The results show that:(1)With the density of carbon containing materials increasing, the porosity of carbonaceous precursors decreases and the infiltrating process of liquid silicon is more difficult.(2)The reaction between carbon containing materials and liquid silicon, the volume effect is more obvious with the density of carbon containing materials increasing.(3)As the carbon containing materials density decreasing, residual carbon in reaction bonded SiC also decreases.

  7. Reactions of carbon cluster ions stored in an RF trap

    International Nuclear Information System (INIS)

    Reactions of carbon cluster ions with O2 were studied by using an RF ion trap in which cluster ions of specific size produced by laser ablation could be stored selectively. Reaction rate constants for positive and negative carbon cluster ions were estimated. In the case of the positive cluster ions, these were consistent with the previous experimental results using FTMS. Negative carbon cluster ions C-n (n=4-8) were much less reactive than positive cluster ions. The CnO- products were seen only in n=4 and 6. (orig.)

  8. Modeling Corrosion Reactions of Steel in a Dilute Carbonate Solution

    Science.gov (United States)

    Eliyan, Faysal Fayez; Alfantazi, Akram

    2016-02-01

    This research models the corrosion reactions of a high-strength steel in an aerated, dilute, carbonate solution during a single-cycle voltammetry. Based on a previous study (Eliyan et al. in J Mater Eng Perform 24(6):1-8, 2015) and a literature survey, the corrosion reactions of the cathodic reduction, anodic dissolution, and passivation, as well as the interfacial interactions and the chemistry of the corrosion products are illustrated in schematics. The paper provides a visual guide on the corrosion reactions for steel in carbonate solutions based on the available mechanistic details that were reported and are still being investigated in literature.

  9. Reaction studies of hot silicon, germanium and carbon atoms

    Energy Technology Data Exchange (ETDEWEB)

    Gaspar, P.P.

    1990-11-01

    The goal of this project was to increase the authors understanding of the interplay between the kinetic and electronic energy of free atoms and their chemical reactivity by answering the following questions: (1) what is the chemistry of high-energy carbon silicon and germanium atoms recoiling from nuclear transformations; (2) how do the reactions of recoiling carbon, silicon and germanium atoms take place - what are the operative reaction mechanisms; (3) how does the reactivity of free carbon, silicon and germanium atoms vary with energy and electronic state, and what are the differences in the chemistry of these three isoelectronic atoms This research program consisted of a coordinated set of experiments capable of achieving these goals by defining the structures, the kinetic and internal energy, and the charge states of the intermediates formed in the gas-phase reactions of recoiling silicon and germanium atoms with silane, germane, and unsaturated organic molecules, and of recoiling carbon atoms with aromatic molecules. The reactions of high energy silicon, germanium, and carbon atoms created by nuclear recoil were studied with substrates chosen so that their products illuminated the mechanism of the recoil reactions. Information about the energy and electronic state of the recoiling atoms at reaction was obtained from the variation in end product yields and the extent of decomposition and rearrangement of primary products (usually reactive intermediates) as a function of total pressure and the concentration of inert moderator molecules that remove kinetic energy from the recoiling atoms and can induce transitions between electronic spin states. 29 refs.

  10. Optical Excitation of Carbon Nanotubes Drives Localized Diazonium Reactions.

    Science.gov (United States)

    Powell, Lyndsey R; Piao, Yanmei; Wang, YuHuang

    2016-09-15

    Covalent chemistries have been widely used to modify carbon nanomaterials; however, they typically lack the precision and efficiency required to directly engineer their optical and electronic properties. Here, we show, for the first time, that visible light which is tuned into resonance with carbon nanotubes can be used to drive their functionalization by aryldiazonium salts. The optical excitation accelerates the reaction rate 154-fold (±13) and makes it possible to significantly improve the efficiency of covalent bonding to the sp(2) carbon lattice. Control experiments suggest that the reaction is dominated by a localized photothermal effect. This light-driven reaction paves the way for precise nanochemistry that can directly tailor carbon nanomaterials at the optical and electronic levels.

  11. Heterogeneously Catalysed Chemical Reactions in Carbon Dioxide Medium

    DEFF Research Database (Denmark)

    Musko, Nikolai E.

    the selective hydrogenation of unsaturated aldehydes in carbon dioxide medium. It was found that supported tungstosilicic acid catalysts and acidic resin Amberlyst-15 are very effective for performing aldol reactions. The positive influence of temperature and CO2-content on catalyst activity was studied...... useful for the phase behaviour investigations. The direct synthesis of dimethyl carbonate from methanol and CO2 has been investigated for quite a long time, however hardly any sufficiently active catalysts have been found so far. Nevertheless, optimisation of the phase equilibria of the reaction mixture...... studies of catalytic chemical reactions in dense and supercritical carbon dioxide have been complemented by the theoretical calculations of phase equilibria using advanced thermodynamic models. In the recent years, the use of compressed carbon dioxide as innovative, non-toxic and non-flammable, cheap...

  12. Diagnostic Appraisal of Grade 12 Students' Understanding of Reaction Kinetics

    Science.gov (United States)

    Yan, Yaw Kai; Subramaniam, R.

    2016-01-01

    The study explored grade 12 students' understanding of reaction kinetics, a topic which has not been extensively explored in the chemistry education literature at this level. A 3-tier diagnostic instrument with 11 questions was developed--this format is of very recent origin and has been the subject of only a handful of studies. The findings…

  13. The 12C(12C,α)20Ne and 12C(12C,p)23Na reactions at the Gamow peak via the Trojan Horse Method

    Science.gov (United States)

    Tumino, A.; Spitaleri, C.; Cherubini, S.; Guardo, L.; Gulino, M.; Indelicato, I.; La Cognata, M.; Lamia, L.; Pizzone, R. G.; Puglia, S. M. R.; Rapisarda, G. G.; Romano, S.; Sergi, M. L.; Spartá, R.

    2016-05-01

    A measurement of the 12C(14N,α20Ne)2H and 12C(14N,p23Na)2Hreactions has been performed at a 14N beam energy of 30.0 MeV. The experiment aims to explore the extent to which contributing 24Mg excited states can be populated in the quasi-free reaction off the deuteron in 14N. In particular, the 24Mg excitation region explored in the measurement plays a key role in stellar carbon burning whose cross section is commonly determined by extrapolating high-energy fusion data. From preliminary results, α and proton channels are clearly identified. In particular, ground and first excited states of 20Ne and 23Na play a major role.

  14. The 12C(12C,α20Ne and 12C(12C,p23Na reactions at the Gamow peak via the Trojan Horse Method

    Directory of Open Access Journals (Sweden)

    Tumino A.

    2016-01-01

    Full Text Available A measurement of the 12C(14N,α20Ne2H and 12C(14N,p23Na2Hreactions has been performed at a 14N beam energy of 30.0 MeV. The experiment aims to explore the extent to which contributing 24Mg excited states can be populated in the quasi-free reaction off the deuteron in 14N. In particular, the 24Mg excitation region explored in the measurement plays a key role in stellar carbon burning whose cross section is commonly determined by extrapolating high-energy fusion data. From preliminary results, α and proton channels are clearly identified. In particular, ground and first excited states of 20Ne and 23Na play a major role.

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

    OpenAIRE

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

    2010-01-01

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

  16. Neutrino and antineutrino charge-exchange reactions on 12C

    International Nuclear Information System (INIS)

    We extend the formalism of weak interaction processes, obtaining new expressions for the transition rates, which greatly facilitate numerical calculations, for both neutrino-nucleus reactions and muon capture. Explicit violation of the conserved vector current hypothesis by the Coulomb field, as well as development of a sum-rule approach for inclusive cross sections, has been worked out. We have done a thorough study of exclusive (ground-state) properties of 12B and 12N within the projected quasiparticle random phase approximation (PQRPA). Good agreement with experimental data achieved in this way put into evidence the limitations of the standard RPA and QRPA models, which come from the inability of the RPA to open the p3/2 shell and from the nonconservation of the number of particles in the QRPA. The inclusive neutrino/antineutrino (ν/ν-tilde) reactions 12C(ν,e-)12N and 12C(ν-tilde,e+)12B are calculated within both the PQRPA and the relativistic QRPA. It is found that (i) the magnitudes of the resulting cross sections are close to the sum-rule limit at low energy, but significantly smaller than this limit at high energies, for both ν and ν-tilde; (ii) they increase steadily when the size of the configuration space is augmented, particularly for ν/ν-tilde energies >200 MeV; and (iii) they converge for sufficiently large configuration space and final-state spin. The quasi-elastic 12C(ν,μ-)12N cross section recently measured in the MiniBooNE experiment is briefly discussed. We study the decomposition of the inclusive cross section based on the degree of forbiddenness of different multipoles. A few words are dedicated to the ν/ν-tilde-12C charge-exchange reactions related to astrophysical applications.

  17. 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.

  18. Oxygen electrode reaction in molten carbonate fuel cells. Final report, September 15, 1987--September 14, 1990

    Energy Technology Data Exchange (ETDEWEB)

    Appleby, A.J.; White, R.E.

    1992-07-07

    Molten carbonate fuel cell system is a leading candidate for the utility power generation because of its high efficiency for fuel to AC power conversion, capability for an internal reforming, and a very low environmental impact. However, the performance of the molten carbonate fuel cell is limited by the oxygen reduction reaction and the cell life time is limited by the stability of the cathode material. An elucidation of oxygen reduction reaction in molten alkali carbonate is essential because overpotential losses in the molten carbonate fuel cell are considerably greater at the oxygen cathode than at the fuel anode. Oxygen reduction on a fully-immersed gold electrode in a lithium carbonate melt was investigated by electrochemical impedance spectroscopy and cyclic voltammetry to determine electrode kinetic and mass transfer parameters. The dependences of electrode kinetic and mass transfer parameters on gas composition and temperature were examined to determine the reaction orders and the activation energies. The results showed that oxygen reduction in a pure lithium carbonate melt occurs via the peroxide mechanism. A mass transfer parameter, D{sub O}{sup 1/2}C{sub O}, estimated by the cyclic voltammetry concurred with that calculated by the EIS technique. The temperature dependence of the exchange current density and the product D{sub O}{sup 1/2}C{sub O} were examined and the apparent activation energies were determined to be about 122 and 175 kJ/ mol, respectively.

  19. Carbon dioxide sequestration via olivine carbonation: Examining the formation of reaction products

    Science.gov (United States)

    King, H. E.; Plümper, O.; Putnis, A.

    2009-04-01

    Due to its abundance and natural ability to sequester CO2, olivine has been proposed as one mineral that could be used in the control of CO2 emissions into the atmosphere (Metz, 2005). Large scale peridotite deposits found in locations such as the Western Gneiss Region in Norway could provide in-situ sites for sequestration or the raw materials for ex-situ mineral carbonation. Determining the conditions under which magnesite (MgCO3) forms most efficiently is crucial to conduct a cost effective process. Understanding the development of secondary minerals is particularly important for in-situ methods as these phases can form passivating layers and affect the host rock porosity. The final solution of flow-through experiments conducted at alkaline pH have been shown to be supersaturated with respect to talc and chrysotile (Giammer et al., 2005), although these phases were not found to have precipitated the formation of a passivating, amorphous silica layer has been observed on reacted olivine surfaces (Bearat et al., 2006). By studying magnesite and other products produced during the carbonation of olivine within Teflon lined steel autoclaves we have begun to form a more comprehensive understanding of how these reactions would proceed during sequestration processes. We have performed batch experiments using carbonated saline solutions in the presence of air or gaseous CO2 from 80 to 200 ˚ C. X-ray powder diffraction was used to identify magnesite within the reaction products. Crystals of magnesite up to 20 m in diameter can be observed on olivine grain surfaces with scanning electron microscopy. Secondary reaction products formed a platy layer on olivine surfaces in reactions above 160 ˚ C and below pH 12. Energy dispersive X-ray analysis of the platy layer revealed an increase in Fe concentration. The macroscopically observable red colouration of the reaction products and Raman spectroscopy indicate that hematite is present in these layers. For experiments with

  20. Pattern Formation and Reaction Textures during Dunite Carbonation

    Science.gov (United States)

    Lisabeth, H. P.; Zhu, W.

    2015-12-01

    Alteration of olivine-bearing rocks by fluids is one of the most pervasive geochemical processes on the surface of the Earth. Serpentinized and/or carbonated ultramafic rocks often exhibit characteristic textures on many scales, from polygonal mesh textures on the grain-scale to onion-skin or kernel patterns on the outcrop scale. Strong disequilibrium between pristine ultramafic rocks and common geological fluids such as water and carbon dioxide leads to rapid reactions and coupled mechanical and chemical feedbacks that manifest as characteristic textures. Textural evolution during metasomatic reactions can control effective reaction rates by modulating dynamic porosity and therefore reactant supply and reactive surface area. We run hydrostatic experiments on thermally cracked dunites saturated with carbon dioxide bearing brine at 15 MPa confining pressure and 150°C to explore the evolution of physical properties and reaction textures as carbon mineralization takes place in the sample. Compaction and permeability reduction are observed throughout experiments. Rates of porosity and permeability changes are sensitive to pore fluid chemistry. After reaction, samples are imaged in 3-dimension (3D) using a dual-beam FIB-SEM. Analysis of the high resolution 3D microstructure shows that permeable, highly porous domains are created by olivine dissolution at a characteristic distance from pre-existing crack surfaces while precipitation of secondary minerals such as serpentine and magnesite is limited largely to the primary void space. The porous dissolution channels provide an avenue for fluid ingress, allow reactions to continue and could lead to progressive hierarchical fracturing. Initial modeling of the system indicates that this texture is the result of coupling between dissolution-precipitation reactions and the local stress state of the sample.

  1. Adverse reactions in treatment with lithium carbonate and haloperidol.

    Science.gov (United States)

    Baastrup, P C; Hollnagel, P; Sorensen, R; Schou, M

    1976-12-01

    Hospital records of 425 patients who had been treated simultaneously with lithium carbonate and haloperidol were examined. Adverse reactions in these patients were the same as in patients given lithium alone or haloperidol alone. None of the patients developed a syndrome resembling that described by others in patients treated with a lithium and haloperidol combination. PMID:1036539

  2. Effects of hydrolysis and carbonization reactions on hydrochar production.

    Science.gov (United States)

    Fakkaew, K; Koottatep, T; Polprasert, C

    2015-09-01

    Hydrothermal carbonization (HTC) is a thermal conversion process which converts wet biomass into hydrochar. In this study, a low-energy HTC process named "Two-stage HTC" comprising of hydrolysis and carbonization stages using faecal sludge as feedstock was developed and optimized. The experimental results indicated the optimum conditions of the two-stage HTC to be; hydrolysis temperature of 170 °C, hydrolysis reaction time of 155 min, carbonization temperature of 215 °C, and carbonization reaction time of 100 min. The hydrolysis reaction time and carbonization temperature had a statistically significant effect on energy content of the produced hydrochar. Energy input of the two-stage HTC was about 25% less than conventional HTC. Energy efficiency of the two-stage HTC for treating faecal sludge was higher than that of conventional HTC and other thermal conversion processes such as pyrolysis and gasification. The two-stage HTC could be considered as a potential technology for treating FS and producing hydrochar. PMID:26051497

  3. Heterogeneously Catalysed Aldol Reactions in Supercritical Carbon Dioxide as Innovative and Non-Flammable Reaction Medium

    DEFF Research Database (Denmark)

    Musko, Nikolai; Grunwaldt, Jan-Dierk

    2011-01-01

    Aldol reactions of several aldehydes have been investigated over acidic and basic catalysts in supercritical carbon dioxide at 180 bar and 100 °C. Both acidic (Amberlyst-15, tungstosilicic acid (TSA) on SiO2 and MCM-41) and basic (hydrotalcite) materials showed interesting performance...

  4. Multifragmentation in the 12 GeV proton induced reaction

    International Nuclear Information System (INIS)

    The intermediate mass fragment (IMF) formation in the 12 GeV proton induced reaction on Au target is analyzed by the quantum molecular dynamics model combined with the JAM hadronic cascade model and the non-equilibrated percolation model. We show that the sideward peaked angular distribution of IMF occur in the multifragmentation at very short time scale around 20 fm/c where non-equilibrated features of the residual nucleus fluctuates the nucleon density and fragments in the repulsive Coulomb force are pushed for the sideward direction. (author)

  5. Studying Short-Range Correlations with the ^12C(e,e'pn) Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Subedi, Ramesh

    2007-12-01

    We investigated electron-induced two-nucleon emission from carbon with the goal of being sensitive to and studying short-range correlations using the 12C(e,e'pN) reaction in a triple-coincidence measurement. Two existing high-resolution spectrometers in Hall A at Jefferson Laboratory were used to detect coincident scattered electrons and struck nucleons. A large neutron detector designed and constructed specially for this experiment was used to detect the recoiling neutrons. We performed analysis of the 12C(e,e'pn) reaction, and made direct observation of short-range correlated n-p pairs. From our analysis we conclude that there are 17.9+/-4.5 times more n-p short-range correlated pairs than p-p short-range correlated pairs.

  6. Studying Short-Range Correlations with the 12C(e,e'pn) Reaction

    International Nuclear Information System (INIS)

    We investigated electron-induced two-nucleon emission from carbon with the goal of being sensitive to and studying short-range correlations using the 12C(e,e'pN) reaction in a triple-coincidence measurement. Two existing high-resolution spectrometers in Hall A at Jefferson Laboratory were used to detect coincident scattered electrons and struck nucleons. A large neutron detector designed and constructed specially for this experiment was used to detect the recoiling neutrons. We performed analysis of the 12C(e,e'pn) reaction, and made direct observation of short-range correlated n-p pairs. From our analysis we conclude that there are 17.9+/-4.5 times more n-p short-range correlated pairs than p-p short-range correlated pairs.

  7. Diffusion-reaction compromise the polymorphs of precipitated calcium carbonate

    Institute of Scientific and Technical Information of China (English)

    Han Wang; Wenlai Huang; Yongsheng Han

    2013-01-01

    Diffusion is seldom considered by chemists and materialists in the preparation of materials while it plays an important role in the field of chemical engineering.If we look at crystallization at the atomic level,crystal growth in a solution starts from the diffusion of ions to the growing surface followed by the incorporation of ions into its lattice.Diffusion can be a rate determining step for the growth of crystals.In this paper,we take the crystallization of calcium carbonate as an example to illustrate the microscopic processes of diffusion and reaction and their compromising influence on the morphology of the crystals produced.The diffusion effect is studied in a specially designed three-cell reactor.Experiments show that a decrease of diffusion leads to retardation of supersaturation and the formation of a continuous concentration gradient in the reaction cell,thus promoting the formation of cubic calcite particles.The reaction rate is regulated by temperature.Increase of reaction rate favors the formation of needle-like aragonite particles.When diffusion and reaction play joint roles in the reaction system,their compromise dominates the formation of products,leading to a mixture of cubic and needle-like particles with a controllable ratio.Since diffusion and reaction are universal factors in the preparation of materials,the finding of this paper could be helpful in the controlled synthesis of other materials.

  8. Elastic Scattering of CARBON-14 + CARBON-12, Carbon -14 + OXYGEN-16, and CARBON-14 + OXYGEN-18.

    Science.gov (United States)

    Sterbenz, Stephen Michael

    -nucleon transfer reactions. We have also applied recent group theoretical models of heavy-ion scattering to our data. The single -channel models involving the SO(3,2) and SO(3,1) dynamical symmetries were found to be somewhat more flexible than standard optical models, but were still not able to provide an acceptable gross description of the ^ {14}C+^{12}C and ^{14}C+^ {16}O data. However, a two-channel SO(3,1) dynamical symmetry model in which the elastic transfer amplitude is obtained as the second channel has provided very good fits to individual highly structured angular distributions and better overall reproduction of the datasets than the other models which we have studied.

  9. Effective Permeability Change in Wellbore Cement with Carbon Dioxide Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Um, Wooyong; Jung, Hun Bok; Martin, Paul F.; McGrail, B. Peter

    2011-11-01

    Portland cement, a common sealing material for wellbores for geological carbon sequestration was reacted with CO{sub 2} in supercritical, gaseous, and aqueous phases at various pressure and temperature conditions to simulate cement-CO{sub 2} reaction along the wellbore from carbon injection depth to the near-surface. Hydrated Portland cement columns (14 mm diameter x 90 mm length; water-to-cement ratio = 0.33) including additives such as steel coupons and Wallula basalt fragments were reacted with CO{sub 2} in the wet supercritical (the top half) and dissolved (the bottom half) phases under carbon sequestration condition with high pressure (10 MPa) and temperature (50 C) for 5 months, while small-sized hydrated Portland cement columns (7 mm diameter x 20 mm length; water-to-cement ratio = 0.38) were reacted with CO{sub 2} in dissolved phase at high pressure (10 MPa) and temperature (50 C) for 1 month or with wet CO{sub 2} in gaseous phase at low pressure (0.2 MPa) and temperature (20 C) for 3 months. XMT images reveal that the cement reacted with CO{sub 2} saturated groundwater had degradation depth of {approx}1 mm for 1 month and {approx}3.5 mm for 5 month, whereas the degradation was minor with cement exposure to supercritical CO{sub 2}. SEM-EDS analysis showed that the carbonated cement was comprised of three distinct zones; the innermost less degraded zone with Ca atom % > C atom %, the inner degraded zone with Ca atom % {approx} C atom % due to precipitation of calcite, the outer degraded zone with C atom % > Ca atom % due to dissolution of calcite and C-S-H, as well as adsorption of carbon to cement matrix. The outer degraded zone of carbonated cement was porous and fractured because of dissolution-dominated reaction by carbonic acid exposure, which resulted in the increase in BJH pore volume and BET surface area. In contrast, cement-wet CO{sub 2}(g) reaction at low P (0.2 MPa)-T (20 C) conditions for 1 to 3 months was dominated by precipitation of micron

  10. Effect of $^{12}C+$ $^{12}C$ Reaction & Convective Mixing on the Progenitor Mass of ONe White Dwarfs

    CERN Document Server

    Halabi, Ghina M

    2014-01-01

    Stars in the mass range ~8 - 12 $M_{\\odot }$ are the most numerous massive stars. This mass range is critical because it may lead to supernova (SN) explosion, so it is important for the production of heavy elements and the chemical evolution of the galaxy. We investigate the critical transition mass ($M_{up}$), which is the minimum initial stellar mass that attains the conditions for hydrostatic carbon burning. Stars of masses < $M_{up}$ evolve to the Asymptotic Giant Branch and then develop CO White Dwarfs, while stars of masses $\\geqslant $ $M_{up}$ ignite carbon in a partially degenerate CO core and form electron degenerate ONe cores. These stars evolve to the Super AGB (SAGB) phase and either become progenitors of ONe White Dwarfs or eventually explode as electron-capture SN (EC-SN). We study the sensitivity of $M_{up}$ to the C-burning reaction rate and to the treatment of convective mixing. In particular, we show the effect of a recent determination of the $^{12}C+$ $^{12}C$ fusion rate, as well as t...

  11. Chemical Reactions in the Processing of Mosi2 + Carbon Compacts

    Science.gov (United States)

    Jacobson, Nathan S.; Lee, Kang N.; Maloy, Stuart A.; Heuer, Arthur H.

    1993-01-01

    Hot-pressing of MoSi2 powders with carbon at high temperatures reduces the siliceous grain boundary phase in the resultant compact. The chemical reactions in this process were examined using the Knudsen cell technique. A 2.3 wt pct oxygen MoSi2 powder and a 0.59 wt pct oxygen MoSi2 powder, both with additions of 2 wt pct carbon, were examined. The reduction of the siliceous grain boundary phase was examined at 1350 K and the resultant P(SiO)/P(CO) ratios interpreted in terms of the SiO(g) and CO(g) isobars on the Si-C-O predominance diagram. The MoSi2 + carbon mixtures were then heated at the hot-pressing temperature of 2100 K. Large weight losses were observed and could be correlated with the formation of a low-melting eutectic and the formation and vaporization of SiC.

  12. Carbon encapsulated magnetic nanoparticles produced by hydrothermal reaction

    Institute of Scientific and Technical Information of China (English)

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

    2007-01-01

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

  13. α-clustering effects in dissipative 12C + 12C reactions at 95 MeV

    Science.gov (United States)

    Baiocco, G.; Morelli, L.; Gulminelli, F.; D'Agostino, M.; Bruno, M.; Abbondanno, U.; Barlini, S.; Bini, M.; Carboni, S.; Casini, G.; Cinausero, M.; Degerlier, M.; Gramegna, F.; Kravchuk, V. L.; Marchi, T.; Olmi, A.; Pasquali, G.; Piantelli, S.; Raduta, Ad. R.

    2013-05-01

    Dissipative 12C+12C reactions at 95 MeV are fully detected in charge with the GARFIELD and RCo apparatuses at Laboratori Nazionali di Legnaro. A comparison to a dedicated Hauser-Feshbach calculation allows us to select events which correspond, to a large extent, to the statistical evaporation of highly excited 24Mg, as well as to extract information on the isotopic distribution of the evaporation residues in coincidence with their complete evaporation chain. Residual deviations from statistical behavior are observed in α yields and attributed to the persistence of cluster correlations well above the 24Mg threshold for six-α decay.

  14. \\alpha-clustering effects in dissipative 12C+12C reactions at 95 MeV

    CERN Document Server

    Baiocco, G; Gulminelli, F; D'Agostino, M; Bruno, M; Abbondanno, U; Barlini, S; Bini, M; Carboni, S; Casini, G; Cinausero, M; Gramegna, M Degerlier F; Kravchuk, V L; Marchi, T; Olmi, A; Pasquali, G; Piantelli, S; Raduta, Ad R

    2013-01-01

    Dissipative 12C+12C reactions at 95 MeV are fully detected in charge with the GARFIELD and RCo apparatuses at LNL. A comparison to a dedicated Hauser-Feshbach calculation allows to select events which correspond, to a large extent, to the statistical evaporation of highly excited 24Mg, as well as to extract information on the isotopic distribution of the evaporation residues in coincidence with their complete evaporation chain. Residual deviations from a statistical behaviour are observed in \\alpha yields and attributed to the persistence of cluster correlations well above the 24Mg threshold for 6 \\alpha's decay.

  15. Method for producing bio-fuel that integrates heat from carbon-carbon bond-forming reactions to drive biomass gasification reactions

    Science.gov (United States)

    Cortright, Randy D.; Dumesic, James A.

    2011-01-18

    A low-temperature catalytic process for converting biomass (preferably glycerol recovered from the fabrication of bio-diesel) to synthesis gas (i.e., H.sub.2/CO gas mixture) in an endothermic gasification reaction is described. The synthesis gas is used in exothermic carbon-carbon bond-forming reactions, such as Fischer-Tropsch, methanol, or dimethylether syntheses. The heat from the exothermic carbon-carbon bond-forming reaction is integrated with the endothermic gasification reaction, thus providing an energy-efficient route for producing fuels and chemicals from renewable biomass resources.

  16. The (K-,p) reaction on C12 at KEK

    CERN Document Server

    Magas, V K; Hirenzaki, S; Oset, E; Ramos, A

    2009-01-01

    We study the (K-,p) reaction on C12 with a kaon beam of 1 GeV momentum, paying a special attention to the region of emitted protons having kinetic energy above 600 MeV, which was used to claim a deep kaon nucleus optical potential [1]. The experiment looks for fast protons emitted from the absorption of in flight kaons by nuclei, but in coincidence with at least one charged particle in the decay counters sandwiching the target. The analysis of the data is done in [1] assuming that the coincidence requirement does not change the shape of the final spectra. However our detailed calculations show that this assumption doesn't hold, and, thus, the final conclusion of this experiment is doubtful. We perform Monte Carlo simulation of this reaction. The advantage of our method with respect to Green's function method used in [1] is that it allows to account not only for quasi-elastic K- p scattering, but also for the other processes which contribute to the proton spectra. We investigated the effect of the multi-scatte...

  17. Study of redox reactions to split water and carbon dioxide

    Science.gov (United States)

    Arifin, Darwin

    The development of carbon-neutral, environmentally-sustainable energy carrier is a technological imperative necessary to mitigate the impact of anthropogenic carbon dioxide on earth's climate. One compelling approach rapidly gaining international attention is the conversion of solar energy into renewable fuels, such as H2 or CO, via a two-step thermochemical cycle driven by concentrated solar power. In accordance with the increased interest in this process, there is a need to better understand the gas splitting chemistry on the metal oxide intermediates encountered in such solar-driven processes. Here we measured the H2 and CO production rates during oxidation by H2O and CO2 in a stagnation flow reactor. Redox cycles were performed over various metal oxide chemistries such as hercynite and ceria based materials that are thermally reduced by laser irradiation. In addition to cycle capacity evaluation, reaction kinetics intrinsic to the materials were extracted using a model-based analytical approach to account for the effects of mixing and dispersion in the reactor. Investigation of the "hercynite chemistry" with raman spectroscopy verifies that, at the surface, the cycle proceeds by stabilizing the reduced and oxidized moieties in two different compounds, which allows the thermal reduction reaction to occur to a greater extent at a temperature 150 °C lower than a similarly prepared CoFe2O4-coated m-ZrO2. Investigation of the ceria cycle shows that the water splitting reaction, in the range of 750 - 950 °C and 20 - 40 vol.% H2O, can best be described by a first-order kinetic model with low apparent activation energy (29 kJ/mol). The carbon dioxide splitting reaction, in the range of 650 - 875 °C and 10 - 40 vol.% CO2, is a more complex surface-mediated phenomena that is controlled by a temperature-dependent surface site blocking mechanism involving adsorbed carbon. Moreover, we find that lattice substitution of ceria with zirconium can increase H2 production by

  18. Sarcoidosis patient: an unexpected reaction to carbonic anhydrase enzyme inhibitor

    OpenAIRE

    Khedr, Yahya A H; Khedr, Abdulla H

    2013-01-01

    Ocular diseases are very common in many of the systemic diseases such as sarcoidosis, and may sometimes be the presenting symptom of the disease. In this case report, we present an unusual reaction of the sarcoid granuloma to carbonic anhydrase enzyme inhibitors (CAIs), which was encountered in a patient with ocular sarcoidosis. This observation was taken after a 2-week interval between a CT scan orbits and an MRI orbits which showed a decrease in size from 4×3×4 cm to 2.5×2.5×2 cm, respectiv...

  19. Resonance analysis of the {sup 12}C,{sup 13}C({alpha},n) reactions and evaluation of neutron yield data of the reaction

    Energy Technology Data Exchange (ETDEWEB)

    Murata, Toru [AITEL Corp., Tokyo (Japan)

    1998-03-01

    The {sup 12}C({alpha},n){sup 15}O reaction and the {sup 13}C({alpha},n){sup 16}O reaction were analyzed with a resonance formula in the incident {alpha}-particle energy range of 1.0 to 16.0 MeV. With the obtained resonance parameters, branching ratios of the emitted neutrons to the several levels of the residual nucleus and their angular distributions were calculated to obtain the energy spectrum of emitted neutrons. Thick target neutron yield of carbon were also calculated and compared with the experimental data. (author)

  20. An Analysis of the $^{12}$C+$^{12}$C Reaction Using a New Type of Coupling Potential

    CERN Document Server

    Boztosun, I

    2001-01-01

    A new approach has been used to explain the experimental data for the $^{12}$C+$^{12}$C system over a wide energy range in the laboratory system from 32.0 MeV to 126.7 MeV. This new coupled-channels based approach involves replacing the usual first derivative coupling potential by a new, second-derivative coupling potential. This paper first shows and discusses the limitation of the standard coupled-channels theory in the case where one of the nuclei in the reaction is strongly deformed. Then, this new approach is shown to improve consistently the agreement with the experimental data: the elastic scattering, single-2$^{+}$ and mutual-2$^{+}$ excitation inelastic scattering data as well as their 90$^{\\circ}$ elastic and inelastic excitation functions with little energy-dependent potentials. This new approach makes major improvement on all the previous coupled-channels calculations for this system.

  1. The 12C* Hoyle state in the inelastic 12C + 12C reaction and in 24Mg* decay

    Science.gov (United States)

    Morelli, L.; Bruno, M.; D'Agostino, M.; Baiocco, G.; Gulminelli, F.; Abbondanno, U.; Barlini, S.; Bini, M.; Casini, G.; Cinausero, M.; Degerlier, M.; Fabris, D.; Gramegna, F.; Mabiala, J.; Marchi, T.; Olmi, A.; Pasquali, G.; Piantelli, S.; Valdré, S.

    2016-08-01

    The reaction 12C + 12C at 95 MeV has been studied at the Legnaro Laboratories of INFN with the GARFIELD + RCo apparatus. Data have been analyzed in order to investigate the decay of the Hoyle state of 12C*. Two different data selections have been made. The first one corresponds to peripheral binary collisions where the quasi-projectile is excited to the Hoyle state and the target has been left in the ground state. The second selection allows for studying central events with the formation of a 24Mg* and the Hoyle state is obtained as a step of the decay chain. The characteristics of the Hoyle state decay are very similar in the two samples and point to a mainly sequential decay through the population of an intermediate 8Begs, with a small contribution (˜1.1%) from simultaneous three α-particle processes.

  2. Mineral carbonation of gaseous carbon dioxide using a clay-hosted cation exchange reaction.

    Science.gov (United States)

    Kang, Il-Mo; Roh, Ki-Min

    2013-01-01

    The mineral carbonation method is still a challenge in practical application owing to: (1) slow reaction kinetics, (2) high reaction temperature, and (3) continuous mineral consumption. These constraints stem from the mode of supplying alkaline earth metals through mineral acidification and dissolution. Here, we attempt to mineralize gaseous carbon dioxide into calcium carbonate, using a cation exchange reaction of vermiculite (a species of expandable clay minerals). The mineralization is operated by draining NaCI solution through vermiculite powders and continuously dropping into the pool of NaOH solution with CO2 gas injected. The mineralization temperature is regulated here at 293 and 333 K for 15 min. As a result of characterization, using an X-ray powder diffractometer and a scanning electron microscopy, two types of pure CaCO3 polymorphs (vaterite and calcite) are identified as main reaction products. Their abundance and morphology are heavily dependent on the mineralization temperature. Noticeably, spindle-shaped vaterite, which is quite different from a typical vaterite morphology (polycrystalline spherulite), forms predominantly at 333 K (approximately 98 wt%).

  3. Thermal properties of light nuclei from 12C + 12C fusion-evaporation reactions

    Science.gov (United States)

    Morelli, L.; Baiocco, G.; D'Agostino, M.; Gulminelli, F.; Bruno, M.; Abbondanno, U.; Appannababu, S.; Barlini, S.; Bini, M.; Casini, G.; Cinausero, M.; Degerlier, M.; Fabris, D.; Gelli, N.; Gramegna, F.; Kravchuk, V. L.; Marchi, T.; Olmi, A.; Pasquali, G.; Piantelli, S.; Valdré, S.; Raduta, Ad R.

    2014-07-01

    The 12C + 12C reaction at 95 MeV has been studied through the complete charge identification of its products by means of the GARFIELD+RCo experimental set-up at INFN Laboratori Nazionali di Legnaro (LNL). In this paper, the first of a series of two, a comparison to a dedicated Hauser-Feshbach calculation allows selecting a set of dissipative events which corresponds, to a large extent, to the statistical evaporation of highly excited 24Mg. Information on the isotopic distribution of the evaporation residues in coincidence with their complete evaporation chain is also extracted. The set of data puts strong constraints on the behaviour of the level density (LD) of light nuclei above the threshold for particle emission. In particular, a fast increase of the LD parameter with excitation energy is supported by the data. Residual deviations from a statistical behaviour are seen in two specific channels, and tentatively associated with a contamination from direct reactions and/or α-clustering effects. These channels are studied in further details in the second paper of the series.

  4. Thermal properties of light nuclei from $^{12}$C+$^{12}$C fusion-evaporation reactions

    CERN Document Server

    Morelli, L; D'Agostino, M; Gulminelli, F; Bruno, M; Abbondanno, U; Appannababu, S; Barlini, S; Bini, M; Casini, G; Cinausero, M; Degerlier, M; Fabris, D; Gelli, N; Gramegna, F; Kravchuk, V L; Marchi, T; Pasquali, G; Piantelli, S; Valdré, S; Raduta, Ad R

    2014-01-01

    The $^{12}$C+$^{12}$C reaction at 95 MeV has been studied through the complete charge identification of its products by means of the GARFIELD+RCo experimental set-up at INFN Laboratori Nazionali di Legnaro (LNL). In this paper, the first of a series of two, a comparison to a dedicated Hauser-Feshbach calculation allows to select a set of dissipative events which corresponds, to a large extent, to the statistical evaporation of highly excited $^{24}$Mg. Information on the isotopic distribution of the evaporation residues in coincidence with their complete evaporation chain is also extracted. The set of data puts strong constraints on the behaviour of the level density of light nuclei above the threshold for particle emission. In particular, a fast increase of the level density parameter with excitation energy is supported by the data. Residual deviations from a statistical behaviour are seen in two specific channels, and tentatively associated with a contamination from direct reactions and/or $\\alpha$-clusteri...

  5. Methods for synthesizing diethyl carbonate from ethanol and supercritical carbon dioxide by one-pot or two-step reactions in the presence of potassium carbonate

    OpenAIRE

    Gasc, Fabien; Thiebaud-Roux, Sophie; Mouloungui, Zephirin

    2009-01-01

    Carbon dioxide sequestration was studied by synthesizing diethyl carbonate (DEC) from ethanol and CO2 under supercritical conditions in the presence of potassium carbonate as a base. The co-reagent was ethyl iodide or a concentrated strong acid. This sequestration reaction occurs in two steps, which were studied separately and in a one-pot reaction. An organic-inorganic carbonate hybrid, potassium ethyl carbonate (PEC) is generated at the end of the first step. This intermediate was character...

  6. Carbon and oxygen isotope separation by plasma chemical reactions in carbon monoxide glow discharge

    International Nuclear Information System (INIS)

    The separation of carbon and oxygen isotopes in CO glow discharge has been studied. The isotope enrichment in the products was measured by quadru-pole mass spectrometer. The reaction yield and empirical formula of solid phase products were determined by the gas-volumetric analysis. The stable products obtained in our experiment are CO2 and solid polymers formed on the discharge wall. The polymer consists of both carbon and oxygen and the oxygen/carbon mole ratio in the polymer is 0.35±0.05. Thi isotope enrichment coefficients show a strong negative dependence on discharge current though the relative reaction yields have an opposite tendency. Consequently, the maximum isotope enrichment coefficients for 13C in wall deposit of 2.31 and for 18O in CO2 of 1.37 are obtained when the discharge current and the reaction yields are minimum in our experimental range. The experimental results of isotope enrichment have been compared with theoretical values estimated by an analytical model of literature. The dilution mechanism of the isotope enrichment of stable products is inferred from the isotopic distributions of 13C and 18O in products and theoretical predictions for isotope enrichment. (author)

  7. Carbon-coated magnetic palladium: applications in partial oxidation of alcohols and coupling reactions.

    Science.gov (United States)

    Magnetic carbon supported Pd catalyst has been synthesized via in situ generation of nanoferrites and incorporation of carbon from renewable cellulose via calcination; catalyst can be used for oxidation of alcohols, amination reaction and arylation of aryl halides (cross coupli...

  8. Synthesis of beta carbon nitride nanosized crystal through mechanochemical reaction

    CERN Document Server

    Yin Long Wei; Liu Yu Xian; Sui Jin Ling; Wang Jing Min

    2003-01-01

    Nanosized beta carbon nitride (beta-C sub 3 N sub 4), of grain size several tens of nanometres, has been synthesized by mechanochemical reaction processing. The low-cost synthetic method developed facilitates the novel and effective synthesis of nanosized crystalline beta-C sub 3 N sub 4 (a = 6.36 A, c = 4.648 A) powders. The graphite powders were first milled to a nanoscale state, then the nanosized graphite powders were milled in an atmosphere of NH sub 3 gas. It was found that nanosized beta-C sub 3 N sub 4 was formed after high-energy ball milling under an NH sub 3 atmosphere. After thermal annealing, the shape of the beta-C sub 3 N sub 4 changes from flake-like to sphere-like. The nanosized beta-C sub 3 N sub 4 formed was characterized by x-ray diffraction, Fourier transformation infrared spectroscopy, and transmission electron microscopy. A solid-gas reaction mechanism was proposed for the formation of nanosized beta-C sub 3 N sub 4 at room temperature induced by mechanochemical activation.

  9. Behavior of shungite carbon in reactions simulating thermal transformations of coal

    Energy Technology Data Exchange (ETDEWEB)

    Grigor' eva, E.N.; Rozhkova, N.N. [Russian Academy of Science, Moscow (Russian Federation)

    2000-07-01

    The catalytic activity of shungite carbon in reactions of model compounds (tetralin and benzyl phenyl ether) simulating thermolysis of coal was studied. The orders, rate constants, and activation energies of reactions were determined.

  10. Evaluating reaction pathways of hydrothermal abiotic organic synthesis at elevated temperatures and pressures using carbon isotopes

    Science.gov (United States)

    Fu, Qi; Socki, Richard A.; Niles, Paul B.

    2015-04-01

    Experiments were performed to better understand the role of environmental factors on reaction pathways and corresponding carbon isotope fractionations during abiotic hydrothermal synthesis of organic compounds using piston cylinder apparatus at 750 °C and 5.5 kbars. Chemical compositions of experimental products and corresponding carbon isotopic values were obtained by a Pyrolysis-GC-MS-IRMS system. Alkanes (methane and ethane), straight-chain saturated alcohols (ethanol and n-butanol) and monocarboxylic acids (formic and acetic acids) were generated with ethanol being the only organic compound with higher δ13C than CO2. CO was not detected in experimental products owing to the favorable water-gas shift reaction under high water pressure conditions. The pattern of δ13C values of CO2, carboxylic acids and alkanes are consistent with their equilibrium isotope relationships: CO2 > carboxylic acids > alkanes, but the magnitude of the fractionation among them is higher than predicted isotope equilibrium values. In particular, the isotopic fractionation between CO2 and CH4 remained constant at ∼31‰, indicating a kinetic effect during CO2 reduction processes. No "isotope reversal" of δ13C values for alkanes or carboxylic acids was observed, which indicates a different reaction pathway than what is typically observed during Fischer-Tropsch synthesis under gas phase conditions. Under constraints imposed in experiments, the anomalous 13C isotope enrichment in ethanol suggests that hydroxymethylene is the organic intermediate, and that the generation of other organic compounds enriched in 12C were facilitated by subsequent Rayleigh fractionation of hydroxymethylene reacting with H2 and/or H2O. Carbon isotope fractionation data obtained in this study are instrumental in assessing the controlling factors on abiotic formation of organic compounds in hydrothermal systems. Knowledge on how environmental conditions affect reaction pathways of abiotic synthesis of organic

  11. Template-free synthesis of porous graphitic carbon nitride/carbon composite spheres for electrocatalytic oxygen reduction reaction.

    Science.gov (United States)

    Fu, Xiaorui; Hu, Xiaofei; Yan, Zhenhua; Lei, Kaixiang; Li, Fujun; Cheng, Fangyi; Chen, Jun

    2016-01-28

    Porous graphitic carbon nitride/carbon composite spheres were synthesized using melamine and cyanuric acid, and glucose as the carbon nitride and carbon precursor, respectively. The 3D hierarchical composites efficiently catalyzed the oxygen reduction reaction with an onset potential of 0.90 V and a kinetic current density of 23.92 mA cm(-2). These merit their promising applications in fuel cells and metal-air batteries.

  12. Study on Utilization of Carboxyl Group Decorated Carbon Nanotubes and Carbonation Reaction for Improving Strengths and Microstructures of Cement Paste

    Directory of Open Access Journals (Sweden)

    Xiantong Yan

    2016-08-01

    Full Text Available Carbon nanotubes (CNTs have excellent mechanical properties and can be used to reinforce cement-based materials. On the other hand, the reaction product of carbonation with hydroxides in hydrated cement paste can reduce the porosity of cement-based materials. In this study, a novel method to improve the strength of cement paste was developed through a synergy of carbon nanotubes decorated with carboxyl group and carbonation reactions. The experimental results showed that the carboxyl group (–COOH of decorated carbon nanotubes and the surfactant can control the morphology of the calcium carbonate crystal of carbonation products in hydrated cement paste. The spindle-like calcium carbonate crystals showed great morphological differences from those observed in the conventional carbonation of cement paste. The spindle-like calcium carbonate crystals can serve as fiber-like reinforcements to reinforce the cement paste. By the synergy of the carbon nanotubes and carbonation reactions, the compressive and flexural strengths of cement paste were significantly improved and increased by 14% and 55%, respectively, when compared to those of plain cement paste.

  13. Heavy Cluster Knockout Reaction O16(C12,2C12)He4 and the Nature of the C12-C12 Interaction Potential

    Science.gov (United States)

    Joshi, B. N.; Jain, Arun K.; Gupta, Y. K.; Biswas, D. C.; Saxena, A.; John, B. V.; Danu, L. S.; Vind, R. P.; Choudhury, R. K.

    2011-01-01

    The heavy cluster knockout reaction O16(C12,2C12)He4 performed for the first time, reveals the true nature of the C12-C12 interaction. The observed cross section is enhanced by almost 2 orders of magnitude over the conventional zero range distorted wave impulse approximation (DWIA) predictions. An attractive C12-C12 optical potential, as obtained in the folding model, does not explain the enhanced cross section in the finite range (FR) DWIA framework. The inclusion of a hard core of fairly long range ˜3.65fm explains the data. The present investigation of O16(C12,2C12)He4 along with the C12-C12 elastic scattering also proves beyond doubt that the folding model’s deep attractive heavy ion potentials are unsuitable to describe the highly overlapping heavy ions. The application of FR-DWIA opens up new avenues to use the heavy core knockout for the detailed investigation of heavy as well as Borromean halo nuclei.

  14. Studies of reaction mechanism in 12C + 12C system at intermediate energy of 28.7 MeV/N

    International Nuclear Information System (INIS)

    The reaction mechanism in 12C + 12C system at intermediate energy of about 30 MeV/nucleon was studied. The contribution of various reaction mechanisms (inelastic scattering, transfer reactions, compound nucleus reactions, sequential decay following inelastic excitation and transfer) to the total reaction cross section were found. The analysis of inclusive and coincidence spectra shows that sequential fragmentation processes dominate

  15. The Nature of Acid-Catalyzed Acetalization Reaction of 1,2-Propylene Glycol and Acetaldehyde

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Chen; Chen, Hui; Li, Xia; Hu, Jianli; Liang, Baochen [Tianjin University of Technology, Tianjin (China)

    2015-08-15

    We investigated catalytic activity of ion-exchange resins in acetalization of 1,2-propylene glycol with acetaldehyde. The impacts of reaction variables, such as temperature, reaction time, catalyst loading and feedstock composition, on the conversion of 1,2-propylene glycol were measured. The life of the catalyst was also studied. Furthermore, the reaction kinetics of 1,2-propylene glycol acetalization was studied. It was found that reaction rate followed the first order kinetics to acetaldehyde and 1,2-propylene glycol, respectively. Therefore, overall acetalization reaction should follow the second-order reaction kinetics, expressed as r - kC{sup nA}{sub A}C{sup nB}{sub B} = 19.74e{sup -650/T}C{sup 1}{sub A}C{sup 1}{sub B}.

  16. BOREAS TGB-12 Soil Carbon Data over the NSA

    Science.gov (United States)

    Trumbore, Susan; Hall, Forrest G. (Editor); Conrad, Sara K. (Editor); Harden, Jennifer; Sundquist, Eric; Winston, Greg

    2000-01-01

    The BOREAS TGB-12 team made measurements of soil carbon inventories, carbon concentration in soil gases, and rates of soil respiration at several sites to estimate the rates of carbon accumulation and turnover in each of the major vegetation types. TGB-12 data sets include soil properties at tower and selected auxiliary sites in the BOREAS NSA and data on the seasonal variations in the radiocarbon content of CO2 in the soil atmosphere at NSA tower sites. The sampling strategies for soils were designed to take advantage of local fire chronosequences, so that the accumulation of C in areas of moss regrowth could be determined. These data are used to calculate the inventory of C and N in moss and mineral soil layers at NSA sites and to determine the rates of input and turnover (using both accumulation since the last stand-killing fire and radiocarbon data). This data set includes physical parameters needed to determine carbon and nitrogen inventory in soils. The data were collected discontinuously from August 1993 to July 1996. The data are stored in tabular ASCII files.

  17. States of Carbon-12 in the Skyrme Model

    CERN Document Server

    Lau, P H C

    2014-01-01

    The Skyrme model has two Skyrmion solutions of baryon number $12$, with $D_{3h}$ and $D_{4h}$ symmetries. The first has an equilateral triangular shape and the second an extended linear shape, analogous to the triangle and linear chain structures of three alpha particles. We recalculate the moments of inertia of these Skyrmions, and deduce the energies and spins of their quantized rotational excitations. There is a good match with the ground-state band of Carbon-12, and with the recently established rotational band of the Hoyle state. The ratio of the root mean square matter radii also matches the experimental value.

  18. High-Throughput Screening of the Asymmetric Decarboxylative Alkylation Reaction of Enolate-Stabilized Enol Carbonates

    KAUST Repository

    Stoltz, Brian

    2010-06-14

    The use of high-throughput screening allowed for the optimization of reaction conditions for the palladium-catalyzed asymmetric decarboxylative alkylation reaction of enolate-stabilized enol carbonates. Changing to a non-polar reaction solvent and to an electron-deficient PHOX derivative as ligand from our standard reaction conditions improved the enantioselectivity for the alkylation of a ketal-protected,1,3-diketone-derived enol carbonate from 28% ee to 84% ee. Similar improvements in enantioselectivity were seen for a β-keto-ester derived- and an α-phenyl cyclohexanone-derived enol carbonate.

  19. Hybrid direct carbon fuel cells and their reaction mechanisms - a review

    DEFF Research Database (Denmark)

    Deleebeeck, Lisa; Kammer Hansen, Kent

    2014-01-01

    with carbon capture and storage (CCS) due to the high purity of CO2 emitted in the exhaust gas. Direct carbon (or coal) fuel cells (DCFCs) are directly fed with solid carbon to the anode chamber. The fuel cell converts the carbon at the anode and the oxygen at the cathode into electricity, heat and reaction...... is discussed on the fuel cell stack and system levels. The range of DCFC types can be roughly broken down into four fuel cell types: aqueous hydroxide, molten hydroxide, molten carbonate and solid oxide fuel cells. Emphasis is placed on the electrochemical reactions occurring at the anode and the proposed...... mechanism(s) of these reactions for molten carbonate, solid oxide and hybrid direct carbon fuel cells. Additionally, the criteria of choosing the ‘best’ DCFC technology is explored, including system design (continuous supply of solid fuel), performance (power density, efficiency), environmental burden...

  20. Integral measurement of the $^{12}$C(n,p)$^{12}$B reaction up to 10 GeV

    CERN Document Server

    Žugec, P; Bosnar, D; Ventura, A; Mengoni, A; Altstadt, S; Andrzejewski, J; Audouin, L; Barbagallo, M; Bécares, V; Bečvář, F; Belloni, F; Berthoumieux, E; Billowes, J; Boccone, V; Brugger, M; Calviani, M; Calviño, F; Cano-Ott, D; Carrapiço, C; Cerutti, F; Chiaveri, E; Chin, M; Cortés, G; Cortés-Giraldo, M.A; Cosentino, L; Diakaki, M; Domingo-Pardo, C; Dressler, R; Duran, I; Eleftheriadis, C; Ferrari, A; Finocchiaro, P; Fraval, K; Ganesan, S; García, A R; Giubrone, G; Gómez-Hornillos, M B; Gonçalves, I F; González-Romero, E; Griesmayer, E; Guerrero, C; Gunsing, F; Gurusamy, P; Heinitz, S; Jenkins, D G; Jericha, E; Käppeler, F; Karadimos, D; Kivel, N; Kokkoris, M; Krtička, M; Kroll, J; Langer, C; Lederer, C; Leeb, H; Leong, L S; Meo, S Lo; Losito, R; Manousos, A; Marganiec, J; Martínez, T; Massimi, C; Mastinu, P; Mastromarco, M; Mendoza, E; Milazzo, P M; Mingrone, F; Mirea, M; Mondalaers, W; Musumarra, A; Paradela, C; Pavlik, A; Perkowski, J; Plompen, A; Praena, J; Quesada, J; Rauscher, T; Reifarth, R; Riego, A; Roman, F; Rubbia, C; Sarmento, R; Saxena, A; Schillebeeckx, P; Schmidt, S; Schumann, D; Tagliente, G; Tain, J L; Tarrío, D; Tassan-Got, L; Tsinganis, A; Valenta, S; Vannini, G; Variale, V; Vaz, P; Versaci, R; Vermeulen, M J; Vlachoudis, V; Vlastou, R; Wallner, A; Ware, T; Weigand, M; Weiß, C; Wright, T

    2016-01-01

    The integral measurement of the $^{12}$C(n,p)$^{12}$B reaction was performed at the neutron time of flight facility n_TOF at CERN. The total number of $^{12}$B nuclei produced per neutron pulse of the n_TOF beam was determined using the activation technique in combination with a time of flight technique. The cross section is integrated over the n_TOF neutron energy spectrum from reaction threshold at 13.6 MeV to 10 GeV. Having been measured up to 1 GeV on basis of the $^{235}$U(n,f) reaction, the neutron energy spectrum above 200 MeV has been reevaluated due to the recent extension of the cross section reference for this particular reaction, which is otherwise considered a standard up to 200 MeV. The results from the dedicated GEANT4 simulations have been used to evaluate the neutron flux from 1 GeV up to 10 GeV. The experimental results related to the $^{12}$C(n,p)$^{12}$B reaction are compared with the evaluated cross sections from major libraries and with the predictions of different GEANT4 models, which m...

  1. Contribution to the study of reactions induced by a low-energy He3 beam on a C12 target

    International Nuclear Information System (INIS)

    This research thesis reports the study concerning which reaction mode will better describe a nucleus in which the excitation energy is between two extremes. Due to experimental considerations and abilities, this study focuses on light target nuclei and carbon 12. The author describes experimental techniques used for angular distributions (targets, detection system), describes the experimental techniques for activation experiments (experimental set-up, targets, measurement of relative efficient cross section, result analysis, measurement of absolute efficient cross section). The author discusses the experimental results (excitation functions and angular distributions) and the interpretation of elastic scattering results (theoretical background, computation approach, analysis of elastic scattering) and the results of the C12(He3, α)C11 reaction

  2. Controllable-nitrogen doped carbon layer surrounding carbon nanotubes as novel carbon support for oxygen reduction reaction

    Energy Technology Data Exchange (ETDEWEB)

    Kuo, P.L.; Hsu, C.H.; Wu, H.M.; Hsu, W.S. [Department of Chemical Engineering, National Cheng Kung University, Tainan (China); Kuo, D. [Department of Biochemistry, University of Washington, Seattle, WA (United States)

    2012-08-15

    Novel nitrogen-doped carbon layer surrounding carbon nanotubes composite (NC-CNT) (N/C ratio 3.3-14.3 wt.%) as catalyst support has been prepared using aniline as a dispersant to carbon nanotubes (CNTs) and as a source for both carbon and nitrogen coated on the surface of the CNTs, where the amount of doped nitrogen is controllable. The NC-CNT so obtained were characterized with scanning electron microscopy (SEM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption and desorption isotherms. A uniform dispersion of Pt nanoparticles (ca. 1.5-2.0 nm) was then anchored on the surface of NC-CNT by using aromatic amine as a stabilizer. For these Pt/NC-CNTs, cyclic voltammogram measurements show a high electrochemical activity surface area (up to 103.7 m{sup 2} g{sup -1}) compared to the commercial E-TEK catalyst (55.3 m{sup 2} g{sup -1}). In single cell test, Pt/NC-CNT catalyst has greatly enhanced catalytic activity toward the oxygen reduction reaction, resulting in an enhancement of ca. 37% in mass activity compared with that of E-TEK. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  3. Graphitic mesoporous carbon based on aromatic polycondensation as catalyst support for oxygen reduction reaction

    Science.gov (United States)

    Liu, Peng; Kong, Jiangrong; Liu, Yaru; Liu, Qicheng; Zhu, Hongze

    2015-03-01

    Mesoporous carbon is constructed by monolithic polyaromatic mesophase deriving from the hexane insoluble of coal-tar pitch. This carbon material exhibits spherical morphology and layered crystallite, and thereby can be graphitized at 900 °C without destroying the mesoporous structure. Electrochemical measurements indicate that graphitic mesoporous carbon (GMC) support not only improves the activity of Pt electrocatalyst to oxygen reduction reaction (ORR), but also shows higher corrosion resistance than commercial XC-72 carbon black in the acid cathode environment.

  4. Neutrino-Nucleus Reactions and Muon Capture in 12C

    CERN Document Server

    Krmpotic, F; Mariano, A; Mariano, and A.

    2004-01-01

    The neutrino-nucleus cross section and the muon capture rate are discussed within a simple formalism which facilitates the nuclear structure calculations. The corresponding formulae only depend on four types of nuclear matrix elements, which are currently used in the nuclear beta decay. We have also considered the non-locality effects arising from the velocity-dependent terms in the hadronic current. We show that for both observables in 12C the higher order relativistic corrections are of the order of ~5 only, and therefore do not play a significant role. As nuclear model framework we use the projected QRPA (PQRPA) and show that the number projection plays a crucial role in removing the degeneracy between the proton-neutron two quasiparticle states at the level of the mean field. Comparison is done with both the experimental data and the previous shell model calculations. Possible consequences of the present study on the determination of the $\

  5. Correlation between carbon-carbon bond length and the ease of retro Diels-Alder reaction

    Indian Academy of Sciences (India)

    Sambasivarao Kotha; Shaibal Banerjee; Mobin Shaikh

    2014-09-01

    The bond length between C8-C9 in (1′R,4′S,4a′R,8a′S)-6′,7′-dimethyl-1′,4′,4a′,8a′-tetrahydrospiro [cyclopropane-1,9′-[1,4]methanonaphthalene]-5′,8′-dione is 1.571 (2) Å and between C7-C12 is 1.567 (2) Å which are longer than the corresponding bond length for saturated bicyclic systems (1.531-1.535Å). This paper reports the correlation between bond length and the ease of retro Diels−Alder reaction.

  6. High spin levels populated in multinucleon transfer reaction with 480 MeV 12C

    International Nuclear Information System (INIS)

    Two- and three-nucleon stripping reactions induced by 480 MeV 12C have been studied on 12C, 16O, 28Si, 40Ca and 54Fe target nuclei. Discrete levels are fed with cross sections up to 1 mb/sr for d-transfer reactions and one order and two orders of magnitude less for 2p- and 3He-transfer reactions, respectively. These reactions preferentially populate high spin states with stretched configurations. Several spin assignments were known from transfer reactions induced by lighter projectiles at incident energies well above the Coulomb barrier. In the case of two-nucleon transfer reactions, the energy of these states is well reproduced by crude shell model calculations. Such estimates are of use in proposing spins of newly observed states especially as the shapes of the measured angular distributions are independent of the final spin of the residual nucleus

  7. R-matrix analysis of the 12C(α,γ) reaction with inputs from 12C(7Li,t)16O∗ transfer reaction

    International Nuclear Information System (INIS)

    The 12C(α,γ) reaction at 300 keV determines the ratio of 16O to 12C abundance at the end of helium burning in stars. The direct measurement of the cross-section of this reaction is almost impossible with the presently available techniques. Extrapolation of the cross-section or the astrophysical S-factor from higher energy data is presently adopted. There are several direct measurements of the 12C(α,γ) reaction but the lowest energy upto which measurement has been done is only upto 1 MeV. R-matrix extrapolation of the E2 and E1 capture data is complicated by the lack of knowledge of the cluster structure of the 6.92 MeV (2+) and 7.12 MeV (1-) states of 16O. In this paper we report a study of the E2 capture data that is analysed with the ANC of the 6.92 MeV state determined from 12C(7Li,t) alpha transfer measurements

  8. Palladium-catalyzed cross coupling reactions of 4-bromo-6H-1,2-oxazines

    Directory of Open Access Journals (Sweden)

    Reinhold Zimmer

    2009-09-01

    Full Text Available A number of 4-aryl- and 4-alkynyl-substituted 6H-1,2-oxazines 8 and 9 have been prepared in good yields via cross coupling reactions of halogenated precursors 2, which in turn are easily accessible by bromination of 6H-1,2-oxazines 1. Lewis-acid promoted reaction of 1,2-oxazine 9c with 1-hexyne provided alkynyl-substituted pyridine derivative 12 thus demonstrating the potential of this approach for the synthesis of pyridines.

  9. Studies of reductive elimination reactions to form carbon-oxygen bonds from Pt(IV) complexes.

    Science.gov (United States)

    Williams, B S; Goldberg, K I

    2001-03-21

    The platinum(IV) complexes fac-L(2)PtMe(3)(OR) (L(2) = bis(diphenylphosphino)ethane, o-bis(diphenylphosphino)benzene, R = carboxyl, aryl; L = PMe(3), R = aryl) undergo reductive elimination reactions to form carbon-oxygen bonds and/or carbon-carbon bonds. The carbon-oxygen reductive elimination reaction produces either methyl esters or methyl aryl ethers (anisoles) and L(2)PtMe(2), while the carbon-carbon reductive elimination reaction affords ethane and L(2)PtMe(OR). Choice of reaction conditions allows the selection of either type of coupling over the other. A detailed mechanistic study of the reductive elimination reactions supports dissociation of the OR(-) ligand as the initial step for the C-O bond formation reaction. This is followed by a nucleophilic attack of OR(-) upon a methyl group bound to the Pt(IV) cation to produce the products MeOR and L(2)PtMe(2). C-C reductive elimination proceeds from L(2)PtMe(3)(OR) by initial L (L = PMe(3)) or OR(-) (L(2) = dppe, dppbz) dissociation, followed by C-C coupling from the resulting five-coordinate intermediate. Our studies demonstrate that both C-C and C-O reductive elimination reactions from Pt(IV) are more facile in polar solvents, in the presence of Lewis acids, and for OR(-) groups that contain electron withdrawing substituents. PMID:11456927

  10. Carbon dioxide released from subduction zones by fluid-mediated reactions

    Science.gov (United States)

    Ague, Jay J.; Nicolescu, Stefan

    2014-05-01

    The balance between the subduction of carbonate mineral-bearing rocks into Earth's mantle and the return of CO2 to the atmosphere by volcanic and metamorphic degassing is critical to the carbon cycle. Carbon is thought to be released from subducted rocks mostly by simple devolatilization reactions. However, these reactions will also retain large amounts of carbon within the subducting slab and have difficulty in accounting for the mass of CO2 emitted from volcanic arcs. Carbon release may therefore occur via fluid-induced dissolution of calcium carbonate. Here we use carbonate δ18O and δ13C systematics, combined with analyses of rock and fluid inclusion mineralogy and geochemistry, to investigate the alteration of the exhumed Eocene Cycladic subduction complex on the Syros and Tinos islands, Greece. We find that in marble rocks adjacent to two fluid conduits that were active during subduction, the abundance of calcium carbonate drastically decreases approaching the conduits, whereas silicate minerals increase. Up to 60-90% of the CO2 was released from the rocks--far greater than expected via simple devolatilization reactions. The δ18O of the carbonate minerals is 5-10 lighter than is typical for metamorphosed carbonate rocks, implying that isotopically light oxygen was transported by fluid infiltration from the surroundings. We suggest that fluid-mediated carbonate mineral removal, accompanied by silicate mineral precipitation, provides a mechanism for the release of enormous amounts of CO2 from subduction zones.

  11. The Path of Carbon in Photosynthesis IX. Photosynthesis, Photoreduction, and the Hydrogen-Oxygen-Carbon Dioxide Dark Reaction

    Science.gov (United States)

    Badin, E. J.; Calvin, M.

    1950-02-01

    A comparison of the rates of fixation of Carbon 14 dioxide in algae for the processes of photosynthesis, photoreduction and the hydrogen-oxygen-carbon dioxide dark reaction has been made. For the same series of experiments, rates of incorporation of tracer carbon into the separate soluble components using the radiogram method have been determined. The mechanism of carbon dioxide uptake has been shown to occur via two distinct paths. In all cases studied, essentially the same compounds appear radioactive. The distribution with time, however, differs markedly.

  12. Dilepton spectroscopy at intermediate energies; the carbon - carbon reaction at 1 GeV/A

    International Nuclear Information System (INIS)

    The Physics context of this work is heavy ion collisions at relativistic energies where di-electron provide informations on the produced hot and dense nuclear matter. The experiment is performed by the DiLepton Spectrometer (DLS) Collaboration at the Lawrence Berkeley's Bevalac. After a description of the apparatus, we review the whole program and the main results so far obtained: first evidence of a significant di-electron signal at energies above 1 GeV/A; improvement of the understanding of di-electron production (electromagnetic decays of hadrons, π+π- annihilation and hadronic Bremsstrahlung). The results of p-p, p-d reactions from 1 to 4.9 GeV/A show that hadronic Bremsstrahlung (pp, pn) should be reformulated. Our analysis, optimized on the reaction Carbon-Carbon at 1 GeV/A, has been applied to α-Ca and d-Ca. We have developed two main aspects: improvement of the time resolution (500 ps) in order to eliminate all of the protons. Improvement of the space resolution (300 μ) for better mass resolution, in particular in the ρ region. We obtain the cross section of di-electron production as a function of mass, transverse momentum and rapidity from the C-C, α-Ca and d-Ca reactions at 1 GeV/A. We also compare the cross section for all of the measured systems at 1 GeV/A, including Ca-Ca, and we show a (ApAt)α dependence with α ≅ 1.1. A study of the associated multiplicity has also been performed. Nevertheless, the limited acceptance of the DLS and its poor mass resolution to identify the ρ, ω vector mesons, do not allow to conclude on hadron behaviour in nuclear matter. This point is one of the main goal of the HADES project at GSI (Darmstadt), which we give a brief description of the main features. (authors). 60 refs

  13. Observation of Λ-hypernuclei in the reaction 12C(π+,K+)/sub Λ/12C

    International Nuclear Information System (INIS)

    The observation of Λ-hypernuclear levels in /sub Λ/12C by associated production through the (π+,K+) reaction is reported. Spectrometers used in the measurements are discussed. The /sub Λ/12C excitation energy spectra were recorded at laboratory scattering angles of 5.60, 10.30, and 15.20. The spectra show two major peaks - one attributed to the ground state, and one about 11 MeV higher in excitation. The peak near 11 MeV excitation energy is believed to be almost entirely composed of a multiplet of three J/sup π/ = 2+ states. Relativistic DWBA calculations imply support for the expectation that higher spin states are preferentially populated in the (π+,K+) reaction, compared to the (K-,π-) reaction in which lower spin states are excited. 29 refs., 40 figs

  14. Observation of. lambda. -hypernuclei in the reaction /sup 12/C(. pi. /sup +/,K/sup +/)/sub. lambda. //sup 12/C

    Energy Technology Data Exchange (ETDEWEB)

    Milner, E.C.

    1985-12-01

    The observation of ..lambda..-hypernuclear levels in /sub ..lambda..//sup 12/C by associated production through the (..pi../sup +/,K/sup +/) reaction is reported. Spectrometers used in the measurements are discussed. The /sub ..lambda..//sup 12/C excitation energy spectra were recorded at laboratory scattering angles of 5.6/sup 0/, 10.3/sup 0/, and 15.2/sup 0/. The spectra show two major peaks - one attributed to the ground state, and one about 11 MeV higher in excitation. The peak near 11 MeV excitation energy is believed to be almost entirely composed of a multiplet of three J/sup ..pi../ = 2/sup +/ states. Relativistic DWBA calculations imply support for the expectation that higher spin states are preferentially populated in the (..pi../sup +/,K/sup +/) reaction, compared to the (K/sup -/,..pi../sup -/) reaction in which lower spin states are excited. 29 refs., 40 figs.

  15. The role of carbon in the photocatalytic reaction of carbon/TiO{sub 2} photocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Teng, Feng; Zhang, Guozhi; Wang, Youqing; Gao, Caitian; Chen, Lulu; Zhang, Peng; Zhang, Zhenxing, E-mail: zhangzx@lzu.edu.cn; Xie, Erqing, E-mail: xieeq@lzu.edu.cn

    2014-11-30

    Graphical abstract: - Highlights: • Carbon/TiO{sub 2} composites were fabricated by one-step carbonization method. • Carbon was generated by the dehydration carbonation effect of polymers. • Carbon was formed inside and outside of the TiO{sub 2} nanoparticles. • The photocatalytic activities of the composites depend on the coating carbon. - Abstract: The carbon/TiO{sub 2} nanocomposites were fabricated by a simple one-step carbonization method with different polymers as precursors. Due to the dehydration carbonation effect of polymers, carbon was formed inside and outside of the TiO{sub 2} nanoparticles. The photo-degradation study of rhodamine B was carried out under UV–vis light irradiation, and the photocatalytic activities of carbon/TiO{sub 2} nanocomposites are affected severely by the state of carbon, including dopants and coatings. The results show that the carbon on the surface plays more important role in the photocatalytic process.

  16. Determination of astrophysical 12N(p,g)13O reaction rate from the 2H(12N, 13O)n reaction and its astrophysical implications

    CERN Document Server

    Guo, B; Li, Zhihong; Wang, Y B; Yan, S Q; Li, Y J; Shu, N C; Han, Y L; Bai, X X; Chen, Y S; Liu, W P; Yamaguchi, H; Binh, D N; Hashimoto, T; Hayakawa, S; Kahl, D; Kubono, S; He, J J; Hu, J; Xu, S W; Iwasa, N; Kume, N; Li, Zhihuan

    2012-01-01

    The evolution of massive stars with very low-metallicities depends critically on the amount of CNO nuclides which they produce. The $^{12}$N($p$,\\,$\\gamma$)$^{13}$O reaction is an important branching point in the rap-processes, which are believed to be alternative paths to the slow 3$\\alpha$ process for producing CNO seed nuclei and thus could change the fate of massive stars. In the present work, the angular distribution of the $^2$H($^{12}$N,\\,$^{13}$O)$n$ proton transfer reaction at $E_{\\mathrm{c.m.}}$ = 8.4 MeV has been measured for the first time. Based on the Johnson-Soper approach, the square of the asymptotic normalization coefficient (ANC) for the virtual decay of $^{13}$O$_\\mathrm{g.s.}$ $\\rightarrow$ $^{12}$N + $p$ was extracted to be 3.92 $\\pm$ 1.47 fm$^{-1}$ from the measured angular distribution and utilized to compute the direct component in the $^{12}$N($p$,\\,$\\gamma$)$^{13}$O reaction. The direct astrophysical S-factor at zero energy was then found to be 0.39 $\\pm$ 0.15 keV b. By considering ...

  17. Theoretical reaction rates of the $^{12}$C($\\alpha$,$\\gamma$)$^{16}$O reaction from the potential model

    CERN Document Server

    Katsuma, M

    2015-01-01

    The radiative capture cross sections of $^{12}$C($\\alpha$,$\\gamma$)$^{16}$O and derived reaction rates are calculated from the direct capture potential model. The resulting $S$-factor at low energies is found to be dominated by $E$2 transition to the $^{16}$O ground state. The $E$1 and $E$2 $S$-factors at $E_{c.m.}=0.3$ MeV are $S_{E1}\\approx3$ keV~b and $S_{E2}=150^{+41}_{-17}$ keV~b, respectively. The sum of the cascade transition through the excited state of $^{16}$O is $S_{\\rm casc}= 18\\pm4.5$ keV~b. The derived reaction rates at low temperatures seem to be concordant with those from the previous evaluation. For astrophysical applications, our reaction rates below $T_9=3$ are provided in an analytic expression.

  18. Non-statistical decay and $\\alpha$-correlations in the $^{12}$C+$^{12}$C fusion-evaporation reaction at 95 MeV

    CERN Document Server

    Morelli, L; D'Agostino, M; Gulminelli, F; Bruno, M; Abbondanno, U; Appannababu, S; Barlini, S; Bini, M; Casini, G; Cinausero, M; Degerlier, M; Fabris, D; Gelli, N; Gramegna, F; Kravchuk, V L; Marchi, T; Pasquali, G; Piantelli, S; Valdré, S; Raduta, Ad R

    2014-01-01

    Multiple alpha coincidence and correlations are studied in the reaction $^{12}$C+$^{12}$C at 95 MeV for fusion-evaporation events completely detected in charge. Two specific channels with Carbon and Oxygen residues in coincidence with $\\alpha$-particles are addressed, which are associated with anomalously high branching ratios with respect the predictions by Hauser-Feshbach calculations. Triple alpha emission appears kinematically compatible with a sequential emission from a highly excited Mg. The phase space distribution of $\\alpha$-$\\alpha$ coincidences suggests a correlated emission from a Mg compound, leaving an Oxygen residue excited above the threshold for neutron decay. These observations indicate a preferential $\\alpha$ emission of $^{24}$Mg at excitation energies well above the threshold for $6-\\alpha$ decay.

  19. Non-statistical decay and α-correlations in the 12C+12C fusion-evaporation reaction at 95 MeV

    Science.gov (United States)

    Morelli, L.; Baiocco, G.; D'Agostino, M.; Gulminelli, F.; Bruno, M.; Abbondanno, U.; Appannababu, S.; Barlini, S.; Bini, M.; Casini, G.; Cinausero, M.; Degerlier, M.; Fabris, D.; Gelli, N.; Gramegna, F.; Kravchuk, V. L.; Marchi, T.; Olmi, A.; Pasquali, G.; Piantelli, S.; Valdré, S.; Raduta, Ad R.

    2014-07-01

    Multiple alpha coincidences and correlations are studied in the reaction 12C+12C at 95 MeV for fusion-evaporation events completely detected in charge. Two specific channels with carbon and oxygen residues in coincidence with α -particles are addressed, which are associated with anomalously high branching ratios with respect to the predictions of Hauser-Feshbach calculations. Triple alpha emission appears kinematically compatible with a sequential emission from a highly excited Mg. The phase space distribution of α - α coincidences suggests a correlated emission from a Mg compound, leaving an oxygen residue excited above the threshold for neutron decay. These observations indicate a preferential α emission of 24Mg at excitation energies well above the threshold for 6 - α decay.

  20. Evidence of $\\Xi$ hypernuclear production in the $^{12}C(K^{-},K^{+})^{12}_{\\Xi}Be$ reaction

    CERN Document Server

    Khaustov, G V; Barnes, P D; Bassalleck, B; Berdoz, A R; Biglan, A; Bürger, T; Carman, D S; Chrien, R E; Davis, C A; Fischer, H; Franklin, G B; Franz, J; Gan, L; Ichikawa, A; Iijima, T; Imai, K; Kondo, Y; Koran, P; Landry, M R; Lee, L; Lowe, J; Magahiz, R; May, M; McCrady, R G; Meyer, C A; Merrill, F; Motoba, T; Page, S A; Paschke, K; Pile, P H; Quinn, B; Ramsay, W D; Rusek, A; Sawafta, R; Schmitt, H; Schumacher, R A; Stotzer, R W; Sutter, R J; Takeutchi, F; Van Oers, W T H; Yamamoto, K; Yamamoto, Y; Yosoi, M; Zeps, V J

    2000-01-01

    The E885 collaboration utilized the 1.8 GeV/c K^- beam line at the AGS to accumulate 3 x 10^5 (K^-,K^+) events. Xi hypernuclear states are expected to be produced through the reaction K^- + ^{12}C -> K^+ + ^{12}_{Xi}Be. The measured missing-mass spectrum indicates the existence of a signal below the threshold for free Xi production. Although the resolution was not sufficient to resolve discrete hypernuclear states, the excess of events in the region of missing mass, kinematically inaccessible in free Xi production, is compared to theoretical prediction for ^{12}_{Xi}Be production.

  1. Studies of reaction mechanism in {sup 12}C + {sup 12}C system at intermediate energy of 28.7 MeV/N

    Energy Technology Data Exchange (ETDEWEB)

    Magiera, A. [Inst. of Physics, Jagiellonian Univ., Cracow (Poland)

    1996-12-31

    The reaction mechanism in {sup 12}C + {sup 12}C system at intermediate energy of about 30 MeV/nucleon was studied. The contribution of various reaction mechanisms (inelastic scattering, transfer reactions, compound nucleus reactions, sequential decay following inelastic excitation and transfer) to the total reaction cross section were found. The analysis of inclusive and coincidence spectra shows that sequential fragmentation processes dominate. 100 refs, 45 figs, 1 tab

  2. New determination of 12C(α,γ)16O reaction rate

    Science.gov (United States)

    Oulebsir, N.

    2015-12-01

    The reaction 12C(α,γ)16O was investigated through the direct α-transfer reaction (7Li,t) at 28 and 34 MeV incident energies. We determined the reduced α-widths of the sub-threshold 2+ and 1- states of 16O from the DWBA analysis of the transfer reaction 12C(7Li,t)16O performed at two incident energies. The obtained result for the 2+ and 1- sub-threshold resonances as introduced in the R-matrix fitting of radiative capture and elastic-scattering data to determine the E2 and E1 S-factor from 0.01MeV to 4.2MeV in the center-of-mass energy. After determining the astrophysic factor of 12C(α,γ)16O S(E) with Pierre Descouvement code, I determined numerically the new reaction rate of this reaction at a different stellar temperature (0.06 Gk-2 GK). The 12C(α,γ)16O reaction rate at T9 = 0.2 is [7.21-2.25+2.15] × 10-15 cm3 s-1 mol-1. Some comparisons and discussions about our new 12C(α,γ)16O reaction rate are presented. The agreements of the reaction rate below T9 = 2 between our results and with those proposed by NACRE indicate that our results are reliable, and they could be included in the astrophysical reaction rate network.

  3. Somewhere beyond the sea? The oceanic - carbon dioxide - reactions

    Science.gov (United States)

    Meisinger, Philipp; Wittlich, Christian

    2014-05-01

    In correlation to climate change and CO2 emission different campaigns highlight the importance of forests and trees to regulate the concentration of carbon dioxide in the earths' atmosphere. Seeing millions of square miles of rainforest cut down every day, this is truly a valid point. Nevertheless, we often tend to forget what scientists like Spokes try to raise awareness for: The oceans - and foremost deep sea sections - resemble the second biggest deposit of carbon dioxide. Here carbon is mainly found in form of carbonate and hydrogen carbonate. The carbonates are needed by corals and other sea organisms to maintain their skeletal structure and thereby to remain vital. To raise awareness for the protection of this fragile ecosystem in schools is part of our approach. Awareness is achieved best through understanding. Therefore, our approach is a hands-on activity that aims at showing students how the carbon dioxide absorption changes in relation to the water temperature - in times of global warming a truly sensitive topic. The students use standard syringes filled with water (25 ml) at different temperatures (i.e. 10°C, 20°C, 40°C). Through a connector students inject carbon dioxide (25ml) into the different samples. After a fixed period of time, students can read of the remaining amount of carbon dioxide in relation to the given water temperature. Just as with every scientific project, students need to closely monitor their experiments and alter their setups (e.g. water temperature or acidity) according to their initial planning. A digital template (Excel-based) supports the analysis of students' experiments. Overview: What: hands-on, minds -on activity using standard syringes to exemplify carbon dioxide absorption in relation to the water temperature (Le Chatelier's principle) For whom: adjustable from German form 11-13 (age: 16-19 years) Time: depending on the prior knowledge 45-60 min. Sources (extract): Spokes, L.: Wie Ozeane CO2 aufnehmen. Environmental

  4. Biocatalytic carbon capture via reversible reaction cycle catalyzed by isocitrate dehydrogenase.

    Science.gov (United States)

    Xia, Shunxiang; Frigo-Vaz, Benjamin; Zhao, Xueyan; Kim, Jungbae; Wang, Ping

    2014-09-12

    The practice of carbon capture and storage (CCS) requires efficient capture and separation of carbon dioxide from its gaseous mixtures such as flue gas, followed by releasing it as a pure gas which can be subsequently compressed and injected into underground storage sites. This has been mostly achieved via reversible thermochemical reactions which are generally energy-intensive. The current work examines a biocatalytic approach for carbon capture using an NADP(H)-dependent isocitrate dehydrogenase (ICDH) which catalyzes reversibly carboxylation and decarboxylation reactions. Different from chemical carbon capture processes that rely on thermal energy to realize purification of carbon dioxide, the biocatalytic strategy utilizes pH to leverage the reaction equilibrium, thereby realizing energy-efficient carbon capture under ambient conditions. Results showed that over 25 mol of carbon dioxide could be captured and purified from its gas mixture for each gram of ICDH applied for each carboxylation/decarboxylation reaction cycle by varying pH between 6 and 9. This work demonstrates the promising potentials of pH-sensitive biocatalysis as a green-chemistry route for carbon capture.

  5. Influence of reaction parameters on the attachment of a carbon nanofiber layer on Ni foils

    NARCIS (Netherlands)

    Pacheco Benito, Sergio; Lefferts, Leon

    2012-01-01

    Dense carbon (C) and entangled carbon nanofiber (CNF) layers were deposited on nickel foils by decomposition of ethylene in presence of different H2 concentrations at 450 °C for different reaction times. Both C and CNF layer thicknesses increase with time, but samples pre-oxidized at 500 °C normally

  6. Mechanistic aspects of the copolymerization reaction of carbon dioxide and epoxides, using a chiral salen chromium chloride catalyst.

    Science.gov (United States)

    Darensbourg, Donald J; Yarbrough, Jason C

    2002-06-01

    The air-stable, chiral (salen)Cr(III)Cl complex (3), where H(2)salen = N,N'-bis(3,5-di-tert-butyl-salicylidene)-1,2-cyclohexene diamine, has been shown to be an effective catalyst for the coupling of cyclohexene oxide and carbon dioxide to afford poly(cyclohexenylene carbonate), along with a small quantity of its trans-cyclic carbonate. The thus produced polycarbonate contained >99% carbonate linkages and had a M(n) value of 8900 g/mol with a polydispersity index of 1.2 as determined by gel permeation chromatography. The turnover number (TON) and turnover frequency (TOF) values of 683 g of polym/g of Cr and 28.5 g of polym/g of Cr/h, respectively for reactions carried out at 80 degrees C and 58.5 bar pressure increased by over 3-fold upon addition of 5 equiv of the Lewis base cocatalyst, N-methyl imidazole. Although this chiral catalyst is well documented for the asymmetric ring-opening (ARO) of epoxides, in this instance the copolymer produced was completely atactic as illustrated by (13)C NMR spectroscopy. Whereas the mechanism for the (salen)Cr(III)-catalyzed ARO of epoxides displays a squared dependence on [catalyst], which presumably is true for the initiation step of the copolymerization reaction, the rate of carbonate chain growth leading to copolymer or cyclic carbonate formation is linearly dependent on [catalyst]. This was demonstrated herein by way of in situ measurements at 80 degrees C and 58.5 bar pressure. Hence, an alternative mechanism for copolymer production is operative, which is suggested to involve a concerted attack of epoxide at the axial site of the chromium(III) complex where the growing polymer chain for epoxide ring-opening resides. Preliminary investigations of this (salen)Cr(III)-catalyzed system for the coupling of propylene oxide and carbon dioxide reveal that although cyclic carbonate is the main product provided at elevated temperatures, at ambient temperature polycarbonate formation is dominant. A common reaction pathway for

  7. New Condensation Reaction of β-keto-δ-valerolactones, Carbon Disulfide and Alkyl Halides

    Institute of Scientific and Technical Information of China (English)

    You Ming WANG; Yu Xin LI; Su Hua WANG; Zheng Ming LI

    2004-01-01

    β-Keto-δ-valerolactones, which were obtained by reaction of acetoacetate with aldehydes or ketones, reacted with carbon disulfide, alkyl halides and a new condensation reaction was developed. The structures of the products 3 were confirmed by 1HNMR spectra and elemental analysis.

  8. Analytical evaluation of the solid rocket motor nozzle surface recession by the alumina-carbon reaction

    OpenAIRE

    Matsukawa, Yutaka; Sato, Yutaka; 松川 豊; 佐藤 裕

    2008-01-01

    A theoretical model describing the chemical ablation of a solid rocket motor nozzle ablator by the alumina-carbon reaction is presented. An application of it to a typical solid rocket motor with a graphite nozzle ablator indicates a large influence of the reaction on the nozzle surface recession.

  9. Proton and alpha evaporation spectra in low energy 12C and 16O induced reactions

    Indian Academy of Sciences (India)

    E T Mirgle; D R Chakrabarty; V M Datar; Suresh Kumar; A Mitra; H H Oza

    2006-08-01

    Proton and alpha particle spectra have been measured in the 12C+93Nb and 12C+58Ni reactions at E(12C) = 40 and 50 MeV and in the 16O+93Nb reaction at E(16O) = 75 MeV. The spectra are compared with the statistical model calculations. The shapes of the calculated spectra are in agreement with experimental data except for the alpha spectrum in the 12C+93Nb reaction at 40 MeV. The observed evaporation bump is at ∼ 2 MeV lower energy compared to the calculated one. This discrepancy could imply alpha particle emission from a deformed configuration before compound nucleus formation at this near Coulomb barrier beam energy.

  10. Effect of {sup 12}C+{sup 12}C reaction and convective mixing on the progenitor mass of ONe white dwarfs

    Energy Technology Data Exchange (ETDEWEB)

    Halabi, Ghina M., E-mail: gfm01@aub.edu.lb; El Eid, Mounib, E-mail: gfm01@aub.edu.lb [American University of Beirut, Department of Physics, P.O. Box 11-0236, Riad El-Solh, Beirut (Lebanon)

    2015-02-24

    Stars in the mass range ∼8 - 12 M{sub ⊙} are the most numerous massive stars. This mass range is critical because it may lead to supernova (SN) explosion, so it is important for the production of heavy elements and the chemical evolution of the galaxy. We investigate the critical transition mass (M{sub up}), which is the minimum initial stellar mass that attains the conditions for hydrostatic carbon burning. Stars of masses < M{sub up} evolve to the Asymptotic Giant Branch and then develop CO White Dwarfs, while stars of masses ≥ M{sub up} ignite carbon in a partially degenerate CO core and form electron degenerate ONe cores. These stars evolve to the Super AGB (SAGB) phase and either become progenitors of ONe White Dwarfs or eventually explode as electron-capture SN (EC-SN). We study the sensitivity of M{sub up} to the C-burning reaction rate and to the treatment of convective mixing. In particular, we show the effect of a recent determination of the {sup 12}C+{sup 12}C fusion rate, as well as the extension of the convective core during hydrogen and helium burning on M{sub up} in solar metallicity stars. We choose the 9 M{sub ⊙} model to show the detailed characteristics of the evolution with the new C-burning rate.

  11. Preparation of hollow carbon nanospheres at low temperature via new reaction route

    International Nuclear Information System (INIS)

    Hollow carbon nanospheres were obtained at 200oC via a new reaction route, by using magnesium, hexachloroethane and aluminum trichloride as starting materials and benzene as solvent. The products were characterized with X-ray diffraction pattern, transmission electron microscope, high-resolution transmission electron microscope images and Raman spectrum. The reaction conditions are easy to be maintained and controlled. They may provide a new method to produce other carbonaceous materials. A possible mechanism of reaction was proposed

  12. Measurement and calculation of 238U fission reaction rates induced by neutrons reflected by carbon material

    International Nuclear Information System (INIS)

    To check the data of carbon material reflecting neutrons, the distribution of 238U fission reaction rates induced by D-T fusion neutrons reflected by carbon material was measured by using the small depleted uranium fission chamber and the capturing detector. For comparison, 238U fission rates without carbon material was measured too. The combined standard uncertainty of 238U fission reaction rate is 5.1%-6.4%. The measured results are consistent with the calculated ones with MCNP/4A code and ENDF/B-IV library data in the range of the error

  13. A kinetic study of the reaction of water vapor and carbon dioxide on uranium

    International Nuclear Information System (INIS)

    The kinetic study of the reaction of water vapour and carbon dioxide with uranium has been performed by thermogravimetric methods at temperatures between 160 and 410 deg G in the first case, 350 and 1050 deg C in the second: Three sorts of uranium specimens were used: uranium powder, thin evaporated films, and small spheres obtained from a plasma furnace. The experimental results led in the case of water vapour, to a linear rate of reaction controlled by diffusion at the lower temperatures, and by a surface reaction at the upper ones. In the case of carbon dioxide, a parabolic law has been found, controlled by diffusional processes. (author)

  14. Mechanochemical Reaction of Lanthanum Carbonate with Sodium Hydroxide and Preparation of Lanthanum Oxide Nanoparticle

    Institute of Scientific and Technical Information of China (English)

    李永绣; 周雪珍; 王志强

    2002-01-01

    The preparation of nano sized La2O3 powder by mechanochemical reaction of lanthanum carbonate with sodium hydroxide and subsequent heat treatment was studied using X-ray diffraction, differential thermal and thermo gravimetric analysis and transmission electron microscopy. It was found that the mechanochemical reaction process can be divided into two steps: the first step is the multi-phases mechanochemical reaction of lanthanum carbonate with NaOH to form amorphous lanthanum basic carbonate and lanthanum hydroxide, and the second step is the crystallization of basic lanthanum carbonate with the formula of La2(OH)2(CO3)2*H2O under a quasi-hydrothermal synthesis condition caused by the mechanical ball-milling. The synthesized La2O3 powder appears clearly separated spherical-like monodisperse nano-size particles in which particle size ranges from 30 to 50 nm.

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

    CERN Document Server

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

    2016-01-01

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

  16. Carbon Isotopic Fractionation in Fischer-Tropsch Type Reactions and Relevance to Meteorite Organics

    Science.gov (United States)

    Johnson, Natasha M; Elsila, Jamie E.; Kopstein, Mickey; Nuth, Joseph A., III

    2012-01-01

    Fischer-Tropsch-Type (FTT) reactions have been hypothesized to contribute to the formation of organic compounds in the early solar system, but it has been difficult to identify a signature of such reactions in meteoritic organics. The work reported here examined whether temperature-dependent carbon isotopic fractionation of FTT reactions might provide such a signature. Analyses of bulk organic deposits resulting from FTT experiments show a slight trend towards lighter carbon isotopic ratios with increasing temperature. It is unlikely, however, that these carbon isotopic signatures could provide definitive provenance for organic compounds in solar system materials produced through FTT reactions, because of the small scale of the observed fractionations and the possibility that signatures from many different temperatures may be present in any specific grain.

  17. Research of Hydrogen Preparation with Catalytic Steam-Carbon Reaction Driven by Photo-Thermochemistry Process

    Directory of Open Access Journals (Sweden)

    Xiaoqing Zhang

    2013-01-01

    Full Text Available An experiment of hydrogen preparation from steam-carbon reaction catalyzed by K2CO3 was carried out at 700°C, which was driven by the solar reaction system simulated with Xenon lamp. It can be found that the rate of reaction with catalyst is 10 times more than that without catalyst. However, for the catalytic reaction, there is no obvious change for the rate of hydrogen generation with catalyst content range from 10% to 20%. Besides, the conversion efficiency of solar energy to chemical energy is more than 13.1% over that by photovoltaic-electrolysis route. An analysis to the mechanism of catalytic steam-carbon reaction with K2CO3 is given, and an explanation to the nonbalanced [H2]/[CO + 2CO2] is presented, which is a phenomenon usually observed in experiment.

  18. Reactions between sodium and various carbon bearing compounds

    International Nuclear Information System (INIS)

    The presence of carbon bearing materials in liquid sodium is undesirable because of their ability to carburise stainless steel components. It has been demonstrated for example that carbon taken up by stainless steels can affect their mechanical properties and that thinner sectioned material such as fuel cladding and the tubing of intermediate heat exchanger may be more sensitive to such effects. Generally speaking, there are a number of potential carbon sources in reactor systems. Some of the sources such as the graphite in neutron shield rods, boron carbide in control rods and carbide fuels are part of the reactor designs while others such as oil in mechanical pumps arid 'coupling-fluids' used to inspect plant components are associated with the respective operation arid inspection of the plant. In this paper it is intended to discuss in general terms the way these various compounds behave in liquid sodium and to assess what effect their presence will have on the materials of construction in fast reactor systems. The paper also reviews the chemistry of the environment in relation to the types of carburizing species which may exist in sodium systems

  19. Kinetics of synthesis of Li4Ti5O12 through solid-solid reaction

    Institute of Scientific and Technical Information of China (English)

    CHOU Kuo-Chih; QIU Weihua; WU Ke; ZHANG Guohua

    2006-01-01

    Solid-solid reaction under low heat or low temperature is an approach to synthesize various kinds of materials that were widely used in electrochemistry field. In this paper a theoretical treatment has been presented for analyzing the mechanism of solid-solid reaction and deriving a series of formulae to describe the variation and rate of reactions. This new model has been used in the manufacturing of spinel Li4Ti5O12. The results show that this new model works very well and will play a useful role for guiding the manufacturing of electrochemical materials.

  20. Chemical Reactions and Kinetics of the Carbon Monoxide Coupling in the Presence of Hydrogen

    Institute of Scientific and Technical Information of China (English)

    Fandong Meng; Genhui Xu; Zhenhua Li; Pa Du

    2002-01-01

    The chemical reactions and kinetics of the catalytic coupling reaction of carbon monoxide to diethyl oxalate were studied in the presence of hydrogen over a supported palladium catalyst in the gaseous phase at the typical coupling reaction conditions. The experiments were performed in a continuous flow fixed-bed reactor. The results indicated that hydrogen only reacts with ethyl nitrite to form ethanol, and kinetic studies revealed that the rate-determining step is the surface reaction of adsorbed hydrogen and the ethoxy radical (EtO-). A kinetic model is proposed and a comparison of the observed and calculated conversions showed that the rate expressions are of rather high confidence.

  1. Effect of temperature on kinetic parameters of decomposition reaction of calcium carbonate

    Institute of Scientific and Technical Information of China (English)

    CHEN Hongwei; CHEN Jiangtao; WEI Riguang; SUO Xinliang

    2013-01-01

    In order to investigate the influence of temperature on behavior of calcium carbonate decomposition,especially on kinetic parameters of the decomposition reaction,the analytically pure calcium carbonate was calcined on a self-built large dose thermogravimetric analyzer.The results indicated that,with an increase in the reaction temperature,the reactivity index of calcium carbonate decomposition increased at stage state while the kinetic parameters decreased at stage state.Moreover,both the reaction indices and the kinetic parameters can be divided into three stages and the temperature turning points in different stages were the same.The phase boundary reaction (cylindrical symmetry) theory was more suitable for calcium carbonate calcination under N2 atmosphere.The change trend of the logarithm of reaction activation with temperature was similar as that of the pre-exponential factor.There existed good liner relationship and kinetic compensation effect between them.The isokinetic temperature of the CaCO3 calcination was 842 ℃ and the reaction rate constant was 0.104 9 min-1 derived by the compensation coefficients.

  2. Examination of the validity of statistical models for the 12C + 12C fusion reaction at sub-barrier energies

    Science.gov (United States)

    Dahlstrom, Erin

    2011-10-01

    Previous experimental studies of 12C + 12C fusion at sub-barrier energies using gamma spectroscopy have been limited by the use of a single detector. Use of the Gammasphere at the Argonne National Laboratory, however, allows for an array of germanium detectors to pick up the characteristic gamma rays, greatly increasing the information received. These decay products do not give us the total cross section for the fusion reaction though; we rely on statistical models that relate them to how the excited states are originally populated and decay. Using a combination of gamma spectroscopy based on data from the Gammasphere and proton spectroscopy from a recent 12C + 12C fusion experiment at Notre Dame, we tested these statistical models. The initial population of excited states for 23Na predicted by Empire, a standard statistical model for the decay of different 24Mg spins, was compared with the population determined from the gamma and proton spectroscopy. This comparison will potentially help us more accurately predict the spin population of 24Mg, further constraining the fusion reaction theory. Thanks: NSF grants PHY-1068192, PHY-0822648; ND REU.

  3. Reaction of folic acid with single-walled carbon nanotubes

    Science.gov (United States)

    Ellison, Mark D.; Chorney, Matthew

    2016-10-01

    The oxygen-containing functional groups on oxidized single-walled carbon nanotubes (SWNTs) are used to covalently bond folic acid molecules to the SWNTs. Infrared spectroscopy confirms intact molecular binding to the SWNTs through the formation of an amide bond between a carboxylic acid group on an SWNT and the primary amine group of folic acid. The folic acid-functionalized SWNTs are readily dispersible in water and phosphate-buffered saline, and the dispersions are stable for a period of two weeks or longer. These folic acid-functionalized SWNTs offer potential for use as biocompatible SWNTs.

  4. Investigation of thermochemistry associated with the carbon-carbon coupling reactions of furan and furfural using ab initio methods.

    Science.gov (United States)

    Liu, Cong; Assary, Rajeev S; Curtiss, Larry A

    2014-06-26

    Upgrading furan and small oxygenates obtained from the decomposition of cellulosic materials via formation of carbon-carbon bonds is critical to effective conversion of biomass to liquid transportation fuels. Simulation-driven molecular level understanding of carbon-carbon bond formation is required to design efficient catalysts and processes. Accurate quantum chemical methods are utilized here to predict the reaction energetics for conversion of furan (C4H4O) to C5-C8 ethers and the transformation of furfural (C5H6O2) to C13-C26 alkanes. Furan can be coupled with various C1 to C4 low molecular weight carbohydrates obtained from the pyrolysis via Diels-Alder type reactions in the gas phase to produce C5-C8 cyclic ethers. The computed reaction barriers for these reactions (∼25 kcal/mol) are lower than the cellulose activation or decomposition reactions (∼50 kcal/mol). Cycloaddition of C5-C8 cyclo ethers with furans can also occur in the gas phase, and the computed activation energy is similar to that of the first Diels-Alder reaction. Furfural, obtained from biomass, can be coupled with aldehydes or ketones with α-hydrogen atoms to form longer chain aldol products, and these aldol products can undergo vapor phase hydrocycloaddition (activation barrier of ∼20 kcal/mol) to form the precursors of C26 cyclic hydrocarbons. These thermochemical studies provide the basis for further vapor phase catalytic studies required for upgrading of furans/furfurals to longer chain hydrocarbons.

  5. Potassium-decorated active carbon supported Co-Mo-based catalyst for water-gas shift reaction

    Institute of Scientific and Technical Information of China (English)

    Yixin Lian; RuiFen Xiao; Weiping Fang; Yiquan Yang

    2011-01-01

    The effect of potassium-decoration was studied on the activity of water-gas shift(WGS)reaction over the Co-Mo-based catalysts supported on active carbon(AC),which was prepared by incipient wetness co-impregnation method.The decoration of potassium on active carbon in advance enhances the activities of the CoMo-K/AC catalysts for WGS reaction.Highest activity(about 92% conversion)was obtained at250 ℃ for the catalyst with an optimum K2O/AC weight ratio in the range from 0.12 to 0.15.The catalysts were characterized by TPR and EPR,and the results show that activated carbon decorated with potassium makes Co-Mo species highly dispersed,and thus easily reduced and sulfurized.XRD results show that an appropriate content of potassium-decoration on active carbon supports may favors the formation of highly dispersed Co9Ss-type structures which are situated on the edge or a site in contact with MoS2,K-Mo-O-S,Mo-S-K phase.Those active species are responsible for the high activity of CoMo-K/AC catalysts.

  6. Synthesis and Some Reactions of 3-Chloro-2-(cyanomethylene-1,2-dihydroquinoxalines

    Directory of Open Access Journals (Sweden)

    Wolfgang Pfleiderer

    2004-03-01

    Full Text Available 2,3-Dichloroquinoxaline and some of its derivatives have been reacted with malononitrile and ethyl cyanoacetate to yield a variety of 3-chloro-2-(cyanomethylene- 1,2-dihydroquinoxaline derivatives. The reaction of 3-chloro-2-(dicyanomethylene-1,2- dihydroquinoxaline (2e with pyridine and its methyl derivatives led to the zwitterionic structures 6a-6c. The structures of the newly synthesized compounds were assigned by spectroscopic data and elemental analyses.

  7. Aligned carbon nanotube with electro-catalytic activity for oxygen reduction reaction

    Science.gov (United States)

    Liu, Di-Jia; Yang, Junbing; Wang, Xiaoping

    2010-08-03

    A catalyst for an electro-chemical oxygen reduction reaction (ORR) of a bundle of longitudinally aligned carbon nanotubes having a catalytically active transition metal incorporated longitudinally in said nanotubes. A method of making an electro-chemical catalyst for an oxygen reduction reaction (ORR) having a bundle of longitudinally aligned carbon nanotubes with a catalytically active transition metal incorporated throughout the nanotubes, where a substrate is in a first reaction zone, and a combination selected from one or more of a hydrocarbon and an organometallic compound containing an catalytically active transition metal and a nitrogen containing compound and an inert gas and a reducing gas is introduced into the first reaction zone which is maintained at a first reaction temperature for a time sufficient to vaporize material therein. The vaporized material is then introduced to a second reaction zone maintained at a second reaction temperature for a time sufficient to grow longitudinally aligned carbon nanotubes over the substrate with a catalytically active transition metal incorporated throughout the nanotubes.

  8. Surface reactions of molecular and atomic oxygen with carbon phosphide films.

    Science.gov (United States)

    Gorham, Justin; Torres, Jessica; Wolfe, Glenn; d'Agostino, Alfred; Fairbrother, D Howard

    2005-11-01

    The surface reactions of atomic and molecular oxygen with carbon phosphide films have been studied using X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Carbon phosphide films were produced by ion implantation of trimethylphosphine into polyethylene. Atmospheric oxidation of carbon phosphide films was dominated by phosphorus oxidation and generated a carbon-containing phosphate surface film. This oxidized surface layer acted as an effective diffusion barrier, limiting the depth of phosphorus oxidation within the carbon phosphide film to phosphorus atoms as well as the degree of phosphorus oxidation. For more prolonged AO exposures, a highly oxidized phosphate surface layer formed that appeared to be inert toward further AO-mediated erosion. By utilizing phosphorus-containing hydrocarbon thin films, the phosphorus oxides produced during exposure to AO were found to desorb at temperatures >500 K under vacuum conditions. Results from this study suggest that carbon phosphide films can be used as AO-resistant surface coatings on polymers.

  9. Characterization of the major reactions during conversion of lignin to carbon fiber

    Directory of Open Access Journals (Sweden)

    Hendrik Mainka

    2015-10-01

    Full Text Available Lightweight design is an essential part of the overall Volkswagen strategy for reducing the CO2 emissions. The use of carbon fiber offers an enormous lightweight potential. In comparison to steel enabling a mass reduction of up to 70% in automotive parts without a degradation of the functionalities is possible. Today, the use of carbon fiber is limited in mass series applications of the automotive industry by the cost of the conventional C-fiber precursor polyacrylonitrile (PAN. 50% of the cost of a conventional carbon fiber already belongs to the cost of the PAN precursor. Lignin as a precursor for carbon fiber production can realize enormous savings in cost. For qualifying lignin-based carbon fiber for automotive mass production a detailed characterization of this new material is necessary. Therefore, nuclear magnetic resonance spectroscopy and Fourier transform infrared spectroscopy are used. Using the results of these experiments, the major reactions during conversion of lignin to carbon fiber are proposed.

  10. Study of the 16O(16O,12C)20Ne reaction mechanism by polarization measurements

    International Nuclear Information System (INIS)

    The 16O(16O,12C)20Ne reaction has been studied at beam energies of 68 and 90 MeV. At these energies, this reaction is selective for populating high spin states well known to have a large overlap with α+16O. The angular distributions have been analyzed with an EFR-DWBA code. Good fits are obtained and the resulting relative α particle spectroscopic factors for the 20Ne states are in good agreement with shell model predictions, and with other results from different α transfer reactions. The polarization of the 20Ne has been measured by angular correlations between 12C and 16O (product of the 20Ne decay). As expected from a semi-classical view of the transfer, a strong 20Ne polarization, on an axis perpendicular to the reaction plane has been found. This polarization remains constant on a wide span of 12C angles. Different nuclear reaction models have been tested. With selected potentials, the DWBA predicts a strong polarization in this case of a heavy ion transfer, but not as strong as the one observed in the experiment. Some possible reasons for this difference are indicated

  11. Probing the statistical decay and alpha-clustering effects in 12c+12c and 14n+10b reactions

    CERN Document Server

    Morelli, Luca; Agostino, M D; Bruno, M; Gulminelli, F; Cinausero, M; Degerlier, M; Fabris, D; Gramegna, F; Marchi, T; Barlini, S; Bini, M; Casini, G; Gelli, N; Lopez, A; Pasquali, G; Piantelli, S; Valdre', S

    2013-01-01

    An experimental campaign has been undertaken at INFN Laboratori Nazionali di Legnaro, Italy, in order to progress in our understanding of the statistical properties of light nuclei at excitation energies above particle emission threshold, by measuring exclusive data from fusion-evaporation reactions. A first reaction 12C+12C at 7.9 AMeV beam energy has been measured, using the GARFIELD+Ring Counter experimental setup. Fusion-evaporation events have been exclusively selected. The comparison to a dedicated Hauser-Feshbach calculation allows us to give constraints on the nuclear level density at high excitation energy for light systems ranging from C up to Mg. Out-of-equilibrium emission has been evidenced and attributed both to entrance channel effects favoured by the cluster nature of reaction partners and, in more dissipative events, to the persistence of cluster correlations well above the 24Mg threshold for 6 alphas decay. The 24Mg compound nucleus has been studied with a new measurement 14N + 10B at 5.7 AM...

  12. Probing the 12C-12C and 12C-16O molecular states by radiative capture reactions: present status and future

    International Nuclear Information System (INIS)

    Complete γ-decay in the 12C(12C,γ)24Mg and 12C(16O,γ)28Si reactions has been measured at energies close to the Coulomb Barrier using the DRAGON spectrometer and its associated BGO γ-array at the TRIUMF facility. The experimental data show an important feeding of doorway states around 10-11 MeV in both reactions. Comparisons with simulations allow to extract the full capture cross section and the main spin involved in the process. Different models are confronted to the results: completely statistical, semi-statistical with an unique entrance spin and cluster. The resolution of the BGO enables to eliminate a fully statistical scenario but is not enough to disentangle the two remaining scenarios. It is shown that the future PARIS array composed of the recently developed LaBr3 scintillators will have capabilities to distinguish between these two scenarios. (authors)

  13. 40 CFR 721.524 - Alcohols, C6-12, ethoxylated, reaction product with maleic anhydride.

    Science.gov (United States)

    2010-07-01

    ... product with maleic anhydride. 721.524 Section 721.524 Protection of Environment ENVIRONMENTAL PROTECTION... with maleic anhydride. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alcohols, C6-12, ethoxylated, reaction product with...

  14. Elusive 2H-1,2-oxasiletes through reactions of an isolable dialkylsilylene with diazocarbonyl compounds.

    Science.gov (United States)

    Dong, Zhaowen; Xiao, Xu-Qiong; Li, Zhifang; Lu, Qiong; Lai, Guoqiao; Kira, Mitsuo

    2015-09-28

    The reactions of isolable dialkysilylene 1 with 2-diazo-1,2-diphenylethanone and ethyl 2-diazo-2-phenylacetate gave elusive silacycles, 2H-1,2-oxasiletes 2 and 3, respectively, in high yields. Because these reactions occur at low temperatures of ca.-30 °C, initial complexation of the silylene to the carbonyl oxygen of the diazocarbonyl compounds is suggested to trigger dinitrogen elimination followed by cyclization. In contrast, a six-membered cyclic diazo compound 8 and 1-sila-2,3-diazabicyclo[3.3.0]oct-3-ene 10 were obtained in good yields by the reaction of 1 with less reactive ethyl 2-diazo-3-oxo-3-phenylpropanoate 7 and trimethylsilyldiazomethane 9. Molecular structures of 2, 3, 8 and 10 were determined by X-ray crystallography.

  15. Synthesis and processing of beta silicon carbide powder by silicon - carbon reaction

    International Nuclear Information System (INIS)

    SiC is an important structural ceramic and finds applications in nuclear industry. Processing of SiC ceramic components for such applications require sinter-active beta silicon carbide powders. Various novel methods have been reported for the synthesis of beta SiC powder based on silica - carbon and silicon - carbon reactions. In this research, beta-silicon carbide (β-SiC) was synthesized from the reaction of Si and C. In this research, beta-silicon carbide (β-SiC) was synthesized from the reaction of Si and C. Stoichiometric amount of silicon and petroleum coke having agglomerate size ∼ 5-8μ were planetarily wet mixed, dried, granulated and compacted to reaction specimens

  16. β-Sialon Produced by Carbon Thermal Nitriding Reaction of Bauxite

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    β-Sialon was produced by carbon thermal nitriding reaction in N2 gas atmosphere when the mixtures of bauxite and anthracite were put into vertical furnace. According to the mass loss of raw materials and the result of X-ray diffration (XRD) of products, the influences of the process parameters on the compositions and relative contents of products, such as the fixed carbon content, the flow of N2, the soaking time and the temperature, were researched.

  17. The Reaction of Carbonates in Contact with Superheated Silicate Melts: New Insights from MEMIN Laser Melting Experiments

    Science.gov (United States)

    Hamann, C.; Hecht, L.; Schäffer, S.; Deutsch, A.; Lexow, B.

    2016-08-01

    The reaction of carbonates in contact with silicate impact melts is discussed quite controversially in the impact community. Here, we discuss four MEMIN laser melting experiments involving carbonates in contact with superheated silicate melts.

  18. Probing the Statistical Decay and α-clustering effects in 12C + 12C and 14N + 10B reactions

    Science.gov (United States)

    Morelli, L.; Baiocco, G.; D'Agostino, M.; Bruno, M.; Gulminelli, F.; Cinausero, M.; Degerlier, M.; Fabris, D.; Gramegna, F.; Marchi, T.; Barlini, S.; Bini, M.; Casini, G.; Gelli, N.; Lopez, A.; Pasquali, G.; Piantelli, S.; Valdrè, S.

    2014-03-01

    An experimental campaign has been undertaken at Laboratori Nazionali di Legnaro (LNL INFN), Italy, in order to progress in our understanding of the statistical properties of light nuclei at excitation energies above particle emission threshold, by measuring exclusive data from fusion-evaporation reactions. On the experimental side, a first reaction: 12C+12C at 95 MeV beam energy has been measured, using the GARFIELD + Ring Counter (RCo) apparatuses. Fusion-evaporation events have been exclusively selected out of the entire data set. The comparison to a dedicated Hauser-Feshbach calculation allows us to give constraints on the nuclear level density at high excitation energy for light systems ranging from C up to Mg. Out-of-equilibrium aα emission has been evidenced and attributed both to an entrance channel effect (favoured by the cluster nature of reaction partners), and, in more dissipative events, to the persistence of cluster correlations well above the 24Mg threshold for 6 α's decay. In order to study the same 24Mg compound nucleus at similar excitation energy with respect to this first reaction a new measurement, 14N + 10B at 5.7 A.MeV, was performed at LNL laboratories with the same experimental setup. The comparison between the two systems would allow us to further constrain the level density of light nuclei in the mass-excitation energy range of interest. In this perspective, deviations from a statistical behaviour can be used as a tool to get information on nuclear clustering, both in the ground-state for projectile and target and in the hot source formed in the collision.

  19. Probing the Statistical Decay and α-clustering effects in 12C + 12C and 14N + 10B reactions

    Directory of Open Access Journals (Sweden)

    Morelli L.

    2014-03-01

    Full Text Available An experimental campaign has been undertaken at Laboratori Nazionali di Legnaro (LNL INFN, Italy, in order to progress in our understanding of the statistical properties of light nuclei at excitation energies above particle emission threshold, by measuring exclusive data from fusion-evaporation reactions. On the experimental side, a first reaction: 12C+12C at 95 MeV beam energy has been measured, using the GARFIELD + Ring Counter (RCo apparatuses. Fusion-evaporation events have been exclusively selected out of the entire data set. The comparison to a dedicated Hauser-Feshbach calculation allows us to give constraints on the nuclear level density at high excitation energy for light systems ranging from C up to Mg. Out-of-equilibrium aα emission has been evidenced and attributed both to an entrance channel effect (favoured by the cluster nature of reaction partners, and, in more dissipative events, to the persistence of cluster correlations well above the 24Mg threshold for 6 α’s decay. In order to study the same 24Mg compound nucleus at similar excitation energy with respect to this first reaction a new measurement, 14N + 10B at 5.7 A.MeV, was performed at LNL laboratories with the same experimental setup. The comparison between the two systems would allow us to further constrain the level density of light nuclei in the mass-excitation energy range of interest. In this perspective, deviations from a statistical behaviour can be used as a tool to get information on nuclear clustering, both in the ground-state for projectile and target and in the hot source formed in the collision.

  20. The study of 12C(α,γ astrophysical reaction using 12C(6Li,d and 12C(7Li,t reaction at 20 MeV and in the framework of the potential model

    Directory of Open Access Journals (Sweden)

    Adhikari S.

    2015-01-01

    Full Text Available The triton angular distribution in the 12C(7Li,t16O reaction has been measured at 20 MeV incident energy. Comparison of the data with Finite Range DWBA and CDCC-CRC calculations show that breakup coupling effects are prominent in the transfer to the ground state. This observation is similar to that in the 12C(6Li,d reaction at the same incident energy. The alpha spectroscopic factor of the 16O ground state is determined (Sα=0.25 from a comparison of the measured angular distribution with respect to the CDCC-CRC calculations. The E2 S-factor of the 12C(α,γ reaction at 300 keV in the framework of a potential model is determined to be about 118 keV-barn.

  1. Initial reaction between CaO and SO2 under carbonating and non-carbonating conditions

    DEFF Research Database (Denmark)

    Rasmussen, Martin Hagsted; Wedel, Stig; Pedersen, Kim H.;

    2015-01-01

    The initial kinetics of the CaO/SO2 reaction have been investigated for reaction times shorter than 1s and in the temperature interval between 450 and 600°C under both carbonating and non-carbonating conditions (0-20 vol% CO2) to clarify how recirculating CaO influences the emission of SO2 from...... showed that the CaO conversion with respect to SO2 declined when the CO2 concentration was increased. Under all conditions, larger specific surface areas of CaO gave higher reaction rates with SO2. Higher temperatures had a positive effect on the reaction between SO2 and CaO under non...... a modern dry kiln preheater system for cement production. Calcined Faxe Bryozo limestone with a particle size smaller than 400μm was utilized as CaO source. It was shown, both theoretically and experimentally, that the observed reaction rates were influenced by mass transport limitations. The results...

  2. Method of carbon chain extension using novel aldol reaction

    Energy Technology Data Exchange (ETDEWEB)

    Silks, Louis A; Gordon, John C; Wu, Ruilan; Hangson, Susan Kloek

    2013-08-13

    Method of producing C.sub.8-C.sub.15 hydrocarbons comprising providing a ketone starting material; providing an aldol starting material comprising hydroxymethylfurfural; mixing the ketone starting material and the aldol starting material in a reaction in the presence of a proline-containing catalyst selected from the group consisting of Zn(Pro).sub.2, Yb(Pro).sub.2, and combinations thereof, or a catalyst having one of the structures (I), (II) or (III), and in the presence of a solvent, wherein the solvent comprises water and is substantially free of organic solvents, where (I), (II) and (III) respectively are: ##STR00001## where R.sub.1 is a C.sub.1-C.sub.6 alkyl moiety, X=(OH) and n=2. ##STR00002## In (III), X may be CH.sub.2, sulfur or selenium, M may be Zn, Mg, or a lanthanide, and R.sub.1 and R.sub.2 each independently may be a methyl, ethyl, phenyl moiety.

  3. Determination of 13C/ 12C ratios with (d, p) nuclear reactions

    Science.gov (United States)

    Wang, Y. Q.; Zhang, J.; Tesmer, J. R.; Li, Y. H.; Greco, R.; Grim, G. P.; Obst, A. W.; Rundberg, R. S.; Wilhelmy, J. B.

    2010-06-01

    Stable isotope ratios such as 13C/ 12C play an important role in many applications including environment and energy research. Since many surface analysis techniques are plagued with unavoidable hydrocarbon contamination issues during analysis, it is highly desirable that 13C and 12C isotopes be measured simultaneously especially in specimens with a minute amount of 13C, in order to reliably determine 13C/ 12C ratios. In this paper, we report that deuterium induced proton particle reactions, 13C(d, p) 14C and 12C(d, p) 13C, provide a convenient and reliable approach for 13C/ 12C ratio determination. Optimizations on experimental considerations and potential interferences from other common light isotopes are discussed as well as results from the application of this technique to diagnose the performance of a target debris collection in an inertial confinement fusion (ICF) experiment.

  4. The process of dimethyl carbonate to diphenyl carbonate: thermodynamics, reaction kinetics and conceptual process design

    NARCIS (Netherlands)

    Haubrock, Jens

    2007-01-01

    Diphenyl carbonate (DPC) is a precursor in the production of Polycarbonate (PC), a widely employed engineering plastic. To overcome the drawbacks of the traditional PC process - e.g. phosgene as a reactant and methylene chloride as solvent- a new process route starting from Dimethyl carbonate (DMC)

  5. Search for $\\Delta^{++}$ component in $^{12}C$ ground state using $^{12}C(\\gamma, \\pi^{+} p)$ reaction

    CERN Document Server

    Bystritsky, V M; Glavanakov, I V; Grabmayr, P; Krechetov, Yu F; Saigushkin, O K; Schuvalov, E N; Tabachenko, A N; Krechetov, Yu. F

    2002-01-01

    The differential cross section for the $^{12}$C$(\\gamma,\\pi^{+}p)$ reaction has been measured in the $\\Delta$(1232) resonance region at high recoil momenta of the residual nuclear system. The data are analyzed under the assumption that the formation of the $\\pi^+p$ pairs may be interpreted as a $\\gamma\\Delta^{++}\\to\\pi^+p$ process which takes place on a $\\Delta^{++}$ preexisting in the target nucleus. Estimates of the $\\Delta^{++}$ momentum distribution $\\rho_{\\Delta^{++}}(\\bar{p})$=0.17 fm$^3$ for a mean momentum $\\bar{p}=300\\pm49$ MeV/c as well as the number of $\\Delta$ isobars per nucleon $N_\\Delta=0.017$ were obtained for $^{12}$C.

  6. Elastic scattering and total reaction cross sections for 8Li+12C

    International Nuclear Information System (INIS)

    Full text: The elastic scattering angular distribution for 8Li on 12C has been measured at ELAB= 23.9 MeV with 8Li radioactive nuclear beam produced by the Radioactive Ion Beams in Brazil facility (RIBRAS). This angular distribution was analysed in terms of optical model with Woods-Saxon and double-folding Sao Paulo potentials. The roles of the breakup and inelastic channels were also investigated with cluster folding and deformed potentials, respectively, through coupled channels calculations. The angular distributions for the proton-transfer 12C(8Li,9Be)11B reaction was also measured at the same energy, simultaneously with the elastic scattering. The spectroscopic factor for the 9Be I 8Li+p> bound system was obtained through DWBA (Distorted-Wave Born Approximation) calculations with the code Fresco, and compared with shell model calculations and other experimental values. The spectroscopic factor obtained was used for normalization of the capture reaction cross section 8Li(p, gamma)9Begs. The depth of the scattered potential obtained was 40,1 +- 1,6 MeV. The astrophysical S-factor curves and the reaction rate for the capture reaction 8Li(p,gamma)9Begs were calculated. Total reaction cross sections for the present system were also extracted from the elastic scattering analysis. A systematic of the reduced reaction cross section obtained from the present and published data on 6;7;8Li isotopes on 12C was performed as a function of energy. (author)

  7. Comprehensive analysis of the metabolome of Pseudomonas putida S12 grown on different carbon sources.

    Science.gov (United States)

    van der Werf, Mariët J; Overkamp, Karin M; Muilwijk, Bas; Koek, Maud M; van der Werff-van der Vat, Bianca J C; Jellema, Renger H; Coulier, Leon; Hankemeier, Thomas

    2008-04-01

    Metabolomics is an emerging, powerful, functional genomics technology that involves the comparative non-targeted analysis of the complete set of metabolites in an organism. We have set-up a robust quantitative metabolomics platform that allows the analysis of 'snapshot' metabolomes. In this study, we have applied this platform for the comprehensive analysis of the metabolite composition of Pseudomonas putida S12 grown on four different carbon sources, i.e. fructose, glucose, gluconate and succinate. This paper focuses on the microbial aspects of analyzing comprehensive metabolomes, and demonstrates that metabolomes can be analyzed reliably. The technical (i.e. sample work-up and analytical) reproducibility was on average 10%, while the biological reproducibility was approximately 40%. Moreover, the energy charge values of the microbial samples generated were determined, and indicated that no biotic or abiotic changes had occurred during sample work-up and analysis. In general, the metabolites present and their concentrations were very similar after growth on the different carbon sources. However, specific metabolites showed large differences in concentration, especially the intermediates involved in the degradation of the carbon sources studied. Principal component discriminant analysis was applied to identify metabolites that are specific for, i.e. not necessarily the metabolites that show those largest differences in concentration, cells grown on either of these four carbon sources. For selected enzymatic reactions, i.e. the glucose-6-phosphate isomerase, triosephosphate isomerase and phosphoglyceromutase reactions, the apparent equilibrium constants (K(app)) were calculated. In several instances a carbon source-dependent deviation between the apparent equilibrium constant (K(app)) and the thermodynamic equilibrium constant (K(eq)) was observed, hinting towards a potential point of metabolic regulation or towards bottlenecks in biosynthesis routes. For glucose-6

  8. Angular Distribution of the 12C(6He, 7Li)11B Reaction

    Institute of Scientific and Technical Information of China (English)

    LI Er-Tao; LI Zhi-Hong; LI Yun-Ju; YAN Sheng-Quan; BAI Xi-Xiang; GUO Bing; SU Jun; WANG You-Bao; WANG Bao-Xiang; LIAN Gang; ZENG Sheng; FANG Xiao; ZHAO Wei-Juan; LIU Wei-Ping

    2009-01-01

    Angular distribution of the 12C(6He, 7Li)11B transfer reaction is measured with a secondary 6He beam of 36.4 Me V for the first time. The experimental angular distribution is well reproduced by the distorted-wave Born approxima-tion (DWBA) calculation. The success of the present experiment shows that it is feasible to measure one-nucleon transfer reaction on a light nucleus target with the secondary beam facility of the HI-13 tandem accelerator at China Institute of Atomic Energy (CIAE), Beifing.

  9. Adsorption structure, thermal reaction and initial pathways of 1,2-benzyne on Cu(100)

    Science.gov (United States)

    Lin, Jong-Liang; Lin, Yi-Shiue; Lin, Bo-Chiuan; Liao, Yuan-Hsuan; Chen, Yi-Ting; Chen, Shang-Wei; Jhuang, Jyun-Yi; Lee, Yarong; Lin, Jiing-Chyuan

    2016-10-01

    1,2-C6H4I2 is used as precursor to generate 1,2-C6H4 (ortho-C6H4) on Cu(100). The reflection-absorption infrared spectroscopy (RAIRS) confirms the vertical adsorption geometry of 1,2-C6H4 on Cu(100), which agrees with that predicted theoretically. H2 evolving between 620 K and 870 K is the only reaction product detected from the 1,2-C6H4 decomposition in temperature-programmed reaction/desorption (TPR/D). Our calculations indicate that the 1,2-C6H4 primarily undergoes C3-H bond scission, forming 1,2,3-C6H3, with distorted C6 ring, and H atom on the surface without ring rupture (C1-C2 bond dissociation) prior to H loss. Furthermore, isomerization of the 1,2-C6H4, if it does occur, may proceed via dehydrogenation-hydrogenation, instead of H-shift.

  10. Oral administration of IL-12 suppresses anaphylactic reactions in a murine model of peanut hypersensitivity.

    Science.gov (United States)

    Lee, S Y; Huang, C K; Zhang, T F; Schofield, B H; Burks, A W; Bannon, G A; Sampson, H A; Li, X M

    2001-11-01

    There is no satisfactory therapeutic intervention for peanut allergy, which accounts for most life-threatening food allergic reactions. Since IL-12 has been found to inhibit allergic airway responses in a mouse model of asthma and to cure Th2 cytokine-mediated murine schistosomiasis, we hypothesized that IL-12 treatment might also inhibit peanut allergic reactions. Consequently, we investigated the effects of oral IL-12 treatment in a murine model of peanut allergy and found that oral administration of liposome encapsulated rIL-12 could both prevent and reverse peanut hypersensitivity and could reduce histamine release, peanut-specific serum IgE and IgG1, and fecal IgA levels. Oral IL-12 treatment also increased IFN-gamma but did not decrease IL-4 or IL-5 levels. We conclude that oral rIL-12 treatment has therapeutic as well as preventive effects on peanut allergy, which are associated with increased IFN-gamma production. PMID:11683581

  11. Heterogeneous reactions of gaseous methanesulfonic acid with calcium carbonate and kaolinite particles

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Heterogeneous reactions of gaseous methanesulfonic acid (MSA) with calcium carbonate (CaCO3) and kaolinite particles at room temperature were investigated using diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and ion chromatography (IC).Methanesulfonate (MS-) was identified as the product in the condensed phase,in accordance with the product of the reaction of gaseous MSA with NaCl and sea salt particles.When the concentration of gaseous MSA was 1.34 × 10-13 molecules cm-3,the uptake coefficient was (1.21 ± 0.06) × 10-8 (1) for the reaction of gaseous MSA with CaCO3 and (4.10 ± 0.65) × 10 10 (1) for the reaction with kaolinite.Both uptake coefficients were significantly smaller than those of the reactions of gaseous MSA with NaCl and sea salt particles.

  12. Carboxylic Group Embedded Carbon Balls as a New Supported Catalyst for Hydrogen Economic Reactions.

    Science.gov (United States)

    Bordoloi, Ankur

    2016-03-01

    Carboxylic group functionalized carbon balls have been successfully synthesized by using a facile synthesis method and well characterized with different characterization techniques such as XPS, MAS NMR, SEM, ICP and N2 physi-sorption analysis. The synthesized material has been effectively utilized as novel support to immobilized ruthenium catalyst for hydrogen economic reactions. PMID:27455763

  13. Mechanisms of oxygen reduction reactions for carbon alloy catalysts via first principles molecular dynamics

    International Nuclear Information System (INIS)

    Carbon alloy catalysts (CACs) are one of promising candidates for platinum-substitute cathode catalysts for polymer electrolyte fuel cells. We have investigated possible mechanisms of oxygen reduction reactions (ORRs) for CACs via first-principles-based molecular dynamics simulations. In this contribution, we review possible ORRs at likely catalytic sites of CACs suggested from our simulations. (author)

  14. Carbophilic versus thiophilic attack in the reaction of metallated aromates and heteroaromates with carbon disulfide

    NARCIS (Netherlands)

    Verkruijsse, H.D.; Brandsma, L.

    1987-01-01

    Copper(I) halides catalyse the formation of carbodithioates RCSSLi in the reaction of aryl- or heteroaryl-lithium reagents with carbon disulfide. Subsequent addition of methyl iodide gives the dithioesters RCSSCH3 in high yields. Appreciable amounts of the methyl sulfides RSCH3 and tars are obtained

  15. Direct Electrochemical Reaction of Horseradish Peroxidase Immobilized on the Surface of Active Carbon Powders

    Institute of Scientific and Technical Information of China (English)

    Dong Mei SUN; Chen Xin CAI; Wei XING; Tian Hong LU

    2004-01-01

    It is reported for the first time that horseradish peroxidase(HRP)immobilized on the active carbon can undergo a direct quasi-reversible electrochemical reaction. In addition,the immobilized HRP showed the stable bioelectrocatalytic activity for the reduction of H2O2.

  16. Carboxylic Group Embedded Carbon Balls as a New Supported Catalyst for Hydrogen Economic Reactions.

    Science.gov (United States)

    Bordoloi, Ankur

    2016-03-01

    Carboxylic group functionalized carbon balls have been successfully synthesized by using a facile synthesis method and well characterized with different characterization techniques such as XPS, MAS NMR, SEM, ICP and N2 physi-sorption analysis. The synthesized material has been effectively utilized as novel support to immobilized ruthenium catalyst for hydrogen economic reactions.

  17. Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions

    DEFF Research Database (Denmark)

    Hansen, Steffen V F; Ulven, Trond

    2015-01-01

    A method for generation of high-quality carbon monoxide by decomposition of oxalyl chloride in an aqueous hydroxide solution is described. The usefulness of the method is demonstrated in the synthesis of heterocycles and for hydroxy-, alkoxy-, amino-, and reductive carbonylation reactions, in sev...

  18. N, S co-doped carbon dots with orange luminescence synthesized through polymerization and carbonization reaction of amino acids

    International Nuclear Information System (INIS)

    Graphical abstract: N, S co-doped CDs with orange luminescence were synthesized through one-pot polymerization and carbonization reactions under hydrothermal conditions, using two different amino acids as raw materials. - Highlights: • N, S co-doped CDs were synthesized by one-pot carbonization reactions, using two different amino acids as raw materials. • The as-obtained N, S co-doped CDs showed unique orange fluorescence under excitation at room temperature. • The products could be applied in the imaging of peritoneal macrophages of mice without any functionalization. - Abstract: For practical application, it is highly desirable to obtain carbon dots (CDs) through environmentally benign synthetic route, using green raw materials. On the other hand, at present, most of CDs reported in the literature showed blue, green and yellow emission. Therefore it is still necessary to develop new strategy to obtain CDs with longer wavelength emission in order to expand their application range. Toward this end, in this study, N, S co-doped CDs were synthesized through one-pot condensation polymerization and carbonization reactions under hydrothermal conditions, using two different amino acids as raw materials. Taking the reaction of L-serine with L-cystine as an example, the as-obtained products were characterized by various techniques such as transmission electron microscopy, elemental analysis, Fourier-transform infrared spectrum, X-ray photoelectron spectra, and so on. Interestingly, N, S co-doped CDs displayed unique orange emission at room temperature. The possible photoluminescence mechanism of N, S co-doped CDs was proposed. Furthermore, the as-synthesized N, S co-doped CDs were directly applied in the imaging of peritoneal macrophages of mice

  19. N, S co-doped carbon dots with orange luminescence synthesized through polymerization and carbonization reaction of amino acids

    Energy Technology Data Exchange (ETDEWEB)

    Zeng, Ya-Wen [Nanomaterials and Chemistry Key Laboratory, Wenzhou University, Wenzhou, Zhejiang 325027 (China); Ma, De-Kun, E-mail: dkma@wzu.edu.cn [Nanomaterials and Chemistry Key Laboratory, Wenzhou University, Wenzhou, Zhejiang 325027 (China); Wang, Wei; Chen, Jing-Jing; Zhou, Lin; Zheng, Yi-Zhou [Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027 (China); Yu, Kang, E-mail: yukang62@126.com [Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027 (China); Huang, Shao-Ming, E-mail: smhuang@wzu.edu.cn [Nanomaterials and Chemistry Key Laboratory, Wenzhou University, Wenzhou, Zhejiang 325027 (China)

    2015-07-01

    Graphical abstract: N, S co-doped CDs with orange luminescence were synthesized through one-pot polymerization and carbonization reactions under hydrothermal conditions, using two different amino acids as raw materials. - Highlights: • N, S co-doped CDs were synthesized by one-pot carbonization reactions, using two different amino acids as raw materials. • The as-obtained N, S co-doped CDs showed unique orange fluorescence under excitation at room temperature. • The products could be applied in the imaging of peritoneal macrophages of mice without any functionalization. - Abstract: For practical application, it is highly desirable to obtain carbon dots (CDs) through environmentally benign synthetic route, using green raw materials. On the other hand, at present, most of CDs reported in the literature showed blue, green and yellow emission. Therefore it is still necessary to develop new strategy to obtain CDs with longer wavelength emission in order to expand their application range. Toward this end, in this study, N, S co-doped CDs were synthesized through one-pot condensation polymerization and carbonization reactions under hydrothermal conditions, using two different amino acids as raw materials. Taking the reaction of L-serine with L-cystine as an example, the as-obtained products were characterized by various techniques such as transmission electron microscopy, elemental analysis, Fourier-transform infrared spectrum, X-ray photoelectron spectra, and so on. Interestingly, N, S co-doped CDs displayed unique orange emission at room temperature. The possible photoluminescence mechanism of N, S co-doped CDs was proposed. Furthermore, the as-synthesized N, S co-doped CDs were directly applied in the imaging of peritoneal macrophages of mice.

  20. Mineral carbonation: energy costs of pretreatment options and insights gained from flow loop reaction studies

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-01-01

    Sequestration of carbon as a stable mineral carbonate has been proposed to mitigate environmental concerns that carbon dioxide may with time escape from its sequestered matrix using alternative sequestration technologies. A method has been developed to prepare stable carbonate products by reacting CO2 with magnesium silicate minerals in aqueous bicarbonate/chloride media at high temperature and pressure. Because this approach is inherently expensive due to slow reaction rates and high capital costs, studies were conducted to improve the reaction rates through mineral pretreatment steps and to cut expenses through improved reactor technology. An overview is given for the estimated cost of the process including sensitivity to grinding and heating as pretreatment options for several mineral feedstocks. The energy costs are evaluated for each pretreatment in terms of net carbon avoided. New studies with a high-temperature, high-pressure flow-loop reactor have yielded information on overcoming kinetic barriers experienced with processing in stirred autoclave reactors. Repeated tests with the flow-loop reactor have yielded insights on wear and failure of system components, on challenges to maintain and measure flow, and for better understanding of the reaction mechanism.

  1. Determination of 55Mn(n,γ) reaction cross-section at the neutron energies of 1.12 and 2.12 MeV

    International Nuclear Information System (INIS)

    In the present work, we determine the 55Mn(n,γ)56Mn reaction cross-section at the neutron energies of 1.12 and 2.12 MeV by using the off-line γ-ray spectrometric technique. The (n,γ) reaction cross-section 55Mn as a function of neutron energy was also calculated using nuclear reaction modular code TALYS-1.6 and compared with the present experimental data at 1.12 and 2.12 MeV as well as the literature data at other neutron energies

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

    Institute of Scientific and Technical Information of China (English)

    Daniel E. Resasco

    2014-01-01

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

  3. Coastal climate reflected in carbon-13/carbon-12 ratio of organic carbon in varved sediment from Santa Barbara basin

    OpenAIRE

    Schimmelmann, Arndt; Tegner, Mia J.

    1991-01-01

    A 1844-1987 time-series of carbon stable isotope ratios from dated sedimentary total organic carbon from the center of the Santa Barbara basin is compared with historical climate and oceanographic records. Carbon derived from carbon-13-depleted phytoplankton and carbon-13-enriched kelp appear responsible for a large part of the isotopic variance in sedimentary total organic carbon. El Niño/Southern Oscillation events are recorded by the isotopic response of marine organic carbon in sediments.

  4. Reactions of B/sub 12r/ with aliphatic free radicals: a pulse-radiolysis study

    International Nuclear Information System (INIS)

    The spectra of the intermediates formed in the reactions of B/sub 12r/ with the free radicals Br2-., CO2-., .CH2C(CH3)2OH, .C(CH3)2OH, . CH2CHO, and .CH(OH)CH2OH are reported. The results indicate that Br2-. oxidizes B/sub 12r/ to B/sub 12a/, via an inner-sphere mechanism, and CO2- . reduces B/sub 12r/ to B/sub 12s/. All the aliphatic free radicals studied, .R, react with B/sub 12r/, yielding as the first product a pseudocoenzyme denoted Co/sup III/-R. Co/sup III/-CH2C(CH3)2OH is stable for over a second in the pH range 3 to 10 as is Co/sup III/-CH2CHO. The latter compound hydrolyzes in acid solutions to yield B/sub 12a/ and CH3CHO. Co/sup III/-C(CH3)2OH and Co/sup III/-CH(OH)CH2OH decompose heterolytically to yield mainly B/sub 12s/; a side reaction that probably yields Co/sup III/-H via a β-hydride shift is also observed. The kinetics of decomposition of Co/sup III/-CH(OH)CH2OH in neutral solutions are reported. No water elimination from the latter intermediate occurs. The reasons for the latter observation are discussed. 6 figures

  5. Drought indicated in carbon-13/carbon-12 ratios of Southwestern tree rings

    International Nuclear Information System (INIS)

    Stomatal closure during periods of moisture deficiency should theoretically lead to elevated 13C/12C ratios as reduction of available CO2 leads to diminished photosynthetic discrimination against 13C in favor of 12C. Stable-carbon isotope ratio chronologies developed from 5-yr tree-ring groups at 17 sites in six southwestern states were tested for a drought relationship by first fitting a spline curve to each chronology to remove the long-term trend and calculating indices as the ratio of actual to spline curve value. The time series of “Del Indices” so developed are significantly correlated with 5-yr mean Palmer Hydrological Drought Indices (post-1930 period) and reconstructed July Palmer Drought Severity Indices from respective areas. Overall, in the period since 1790, the driest pentads were 1900–04 and 1960–64, whereas the wettest were 1980–84 and 1915–19. Maps of drought represented for two pentads seem to be reasonable representations, although spatial correlations of Del Indices with PHDI were generally not significant. These Del Index drought reconstructions may provide a useful measure of past physiological response to drought (stomatal closure), although the present cost of analysis would prevent this from being a routine method. (author)

  6. Shrinkage Cracking: A mechanism for self-sustaining carbon mineralization reactions in olivine rocks

    Science.gov (United States)

    Zhu, W.; Fusseis, F.; Lisabeth, H. P.; Xing, T.; Xiao, X.; De Andrade, V. J. D.; Karato, S. I.

    2015-12-01

    The hydration and carbonation of olivine results in an up to ~44% increase in solid molar volume, which may choke off of fluid supply and passivate reactive surfaces, thus preventing further carbonation reactions. The carbonation of olivine has ben studied extensively in the laboratory. To date, observations from these experimental studies indicate that carbonation reaction rates generally decrease with time and the extent of carbonation is limited in olivine rocks. Field studies, however, show that 100% hydration and carbonation occur naturally in ultramafic rocks. The disagreement between the laboratory results under controlled conditions and the field observations underlines the lack of understanding of the mechanisms responsible for the self-sustaining carbonation interaction in nature. We developed a state-of-the-art pressurized hydrothermal cell that is transparent to X-rays to characterize the real-time evolution of pore geometry during fluid-rock interaction using in-situ synchrotron-based X-ray microtomography. Through a time series of high-resolution 3-dimensional images, we document the microstructural evolution of a porous olivine aggregate reacting with a sodium bicarbonate solution at elevated pressure and temperature conditions. We observed porosity increases, near constant rate of crystal growth, and pervasive reaction-induced fractures. Based on the nanometer scale tomography data, we propose that shrinkage cracking is the mechanism responsible for producing new reactive surface and keep the carbonation reaction self-sustaining in our experiment. Shrinkage cracks are commonly observed in drying mud ponds, cooling lava flows and ice wedge fields. Stretching of a contracting surface bonded to a substrate of nearly constant dimensions leads to a stress buildup in the surface layer. When the stress exceeds the tensile strength, polygonal cracks develop in the surface layer. In our experiments, the stretching mismatch between the surface and interior of

  7. Reaction engineering for materials processing in space: Reduction of ilmenite by hydrogen and carbon monoxide

    Science.gov (United States)

    Zhao, Y.; Shadman, F.

    1991-01-01

    Oxygen is a consumable material which needs to be produced continuously in most space missions. Its use for propulsion as well as life support makes oxygen one of the largest volume chemicals to be produced in space. Production of oxygen from lunar materials is of particular interest and is very attractive possibility. The kinetics and mechanism of reduction of ilmenite by carbon monoxide and hydrogen at 800 to 1100 C were investigated. The temporal profiles of conversion for carbon monoxide have a sigmoidal shape and indicate the presence of three different stages (induction, acceleration, and deceleration) during the reduction reaction. The apparent activation energy decreases from 18 kcal/mole at 10 percent conversion to 10 kcal/mole at 50 percent conversion. The reaction is first order with respect to carbon monoxide under the experimental conditions studied. Both SEM and EDX analysis show that the diffusion of Fe product away from the reaction front and through the TiO2 phase, followed by the nucleation and growth of a separate Fe phase are important steps affecting the process kinetics. The results from hydrogen reduction show that the mechanism of ilmenite reduction by hydrogen is similar to that by carbon monoxide. However, the titanium dioxide can be further reduced by hydrogen at 800 to 1000 C. The detailed comparison and theoretical modeling of both reduction processes is presented.

  8. Changes in a coke structure due to reaction with carbon dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Pusz, S.; Majewska, J.; Pilawa, B. [Centre of Polymer and Carbon Materials, Polish Academy of Sciences, M. Curie-Sklodowskiej 34, PL-41819 Zabrze (Poland); Krzesinska, M. [Centre of Polymer and Carbon Materials, Polish Academy of Sciences, M. Curie-Sklodowskiej 34, PL-41819 Zabrze (Poland); Silesian Technical University, Department of Electron Technology, Institute of Physics, Krzywoustego 2, PL-44100 Gliwice (Poland); Smedowski, L. [Silesian Technical University, Department of Electron Technology, Institute of Physics, Krzywoustego 2, PL-44100 Gliwice (Poland); Kwiecinska, B. [AGH-University of Science and Technology, Aleja Mickiewicza 30, PL-30059 Krakow (Poland)

    2010-04-01

    Technological properties of a coke directly depend on a coke structure, i.e., on carbon matrix (a solid phase in a porous medium) and on pore system. Coke structure is deeply transformed during blast furnace operation and one of the most important factors responsible for that is the CO{sub 2} gasification. The objective of this work was to investigate changes of the physical structure of a coke upon the reaction with carbon dioxide to evaluate the effects of structural transformations on technological properties of a coke. Selected physical parameters of cokes produced in a laboratory scale were carried out prior to and after the reaction with CO{sub 2}. The following physical methods were used for the study: helium gas densitometry, physical adsorption of N{sub 2}, optical microscopy, transmission electron microscopy (TEM), ultrasonic measurements and electron paramagnetic resonance spectroscopy (EPR). The results showed that the reaction with CO{sub 2} distinctly affects the physical structure of coke. Coke solid matrix becomes better ordered, with greater structural units, while development of pore structure consists in the enlargement and coalescence of pores and the increase of specific surface area. Great increase of coke porosity after the reaction with CO{sub 2} seems to be more affecting the final strength and reactivity of coke than the transformation of carbon matrix. (author)

  9. Sulfur reactions and cryptic cross-linkages to oxygen, iron, and carbon cyclin

    Science.gov (United States)

    Druschel, G.; Kafantaris, F. C. A.; Fike, D. A.; Schmitt-Kopplin, P.; Dvorski, S.; Oduro, H.

    2014-12-01

    Sulfur speciation in any setting is controlled by a complex series of redox reactions, polymerization, and complexation reactions that are affected by both biotic and abiotic processes. Additionally there are several crossroads of reactions with oxygen, carbon, and iron in which polysulfide molecules serve as a key reaction component that affects not only sulfur speciation, but the speciation, solubility, and bioavailability of these elements as well. Utilizing a combination of analytical approaches including electrochemistry, spectroscopy, mass spectrometry, and chromatography, we have started to unravel the interconnections between sulfur and other key elements, and how microorganisms may be either direct or indirect contributors to these chemical and mineralogical signatures. In microbial mats, we have observed microbial production of significant hydrogen peroxide under UV-stressed conditions. This peroxide interaction with hydrogen sulfide changes the kinetics and the pathways of abiotic sulfur reactions, potentially affecting the overall bioavailability and isotopic fractionations for specific reactions via a change in the linkage between oxygen and sulfur cycling. In systems containing significant iron, we have observed the production of an electroactive form of ferrous iron and sulfide (FeS(aq)) that is of a size that can be described between a dissolved molecular cluster and a small nanoparticle. This FeS(aq) can be a significant fraction of the dissolved iron or sulfide in a system, and is a key part of both the solubility of iron and sulfur and the pathways potentially important for pyritization reactions. In systems where we investigate the links between sulfur and carbon, laboratory and field experiments indicate a wide range of large and more reduced organic compounds are highly reactive towards polysulfide. Utilizing Fourier-transform ion cyclotron resonance mass spectrometry in conjunction with electrochemistry and chromatography, we are seeing a

  10. CaCO3, its reaction and carbonate rocks: terahertz spectroscopy investigation

    Science.gov (United States)

    Zhan, Honglei; Wu, Shixiang; Zhao, Kun; Bao, Rima; Xiao, Lizhi

    2016-10-01

    Carbonate-rich rocks cover a primary part of the earth’s petroleum geology reservoir. The study of carbonate has special significance and more effective study methods are now needed. In order to improve the availability of carbonate rock detection, terahertz (THz) spectroscopy was employed to investigate relevant materials in Na2CO3  +  CaCl2  =  CaCO3  +  2NaCl, which is often used to generate CaCO3. By comparing the materials composited with different ions, it can be revealed that Ca2+, \\text{CO}32- , Na+ and Cl- have respective absorption features at different frequencies. Furthermore, by utilizing a conservation equation it can be observed that the average refractive indices of Na2CO3 as well as CaCl2 equal those of CaCO3 and NaCl in the entire range. Combining the absorption and refractive effect of the materials in the reaction can comprehensively characterize the different substances and reveal the inner interaction during the reaction. THz spectra can deduce the process of molecule rearrangement in the chemical reaction of long-term rock evolution. Besides, the absorption features of the real carbonate rock collected from the nearest town of Sinan county, Guizhou province in Yunnan-Guizhou plateau validate the peaks’ central frequencies of ions and the principal components of carbonates, which can be in agreement with the SEM-EDS analysis. This research will supply a spectral tool to identify the particles in the rock and deduce an evolution of petroleum carbonate reservoir.

  11. Fabrication and characterization of reaction bonded silicon carbide/carbon nanotube composites

    International Nuclear Information System (INIS)

    Carbon nanotubes have generated considerable excitement in the scientific and engineering communities because of their exceptional mechanical and physical properties observed at the nanoscale. Carbon nanotubes possess exceptionally high stiffness and strength combined with high electrical and thermal conductivities. These novel material properties have stimulated considerable research in the development of nanotube-reinforced composites (Thostenson et al 2001 Compos. Sci. Technol. 61 1899, Thostenson et al 2005 Compos. Sci. Technol. 65 491). In this research, novel reaction bonded silicon carbide nanocomposites were fabricated using melt infiltration of silicon. A series of multi-walled carbon nanotube-reinforced ceramic matrix composites (NT-CMCs) were fabricated and the structure and properties were characterized. Here we show that carbon nanotubes are present in the as-fabricated NT-CMCs after reaction bonding at temperatures above 1400 deg. C. Characterization results reveal that a very small volume content of carbon nanotubes, as low as 0.3 volume %, results in a 75% reduction in electrical resistivity of the ceramic composites. A 96% decrease in electrical resistivity was observed for the ceramics with the highest nanotube volume fraction of 2.1%

  12. Synthesis of graphitic carbon nitride through pyrolysis of melamine and its electrocatalysis for oxygen reduction reaction

    Institute of Scientific and Technical Information of China (English)

    He-Sheng Zhai; Lei Cao; Xing-Hua Xia

    2013-01-01

    Graphitic carbon nitride (g-C3N4) was synthesized via direct pyrolysis of melamine and its electrocatalysis toward oxygen reduction reaction was studied.The morphology and structures of the products were characterized by scanning electron microscope and X-ray powder diffractometer.It was found that higher pyrolysis temperature resulted in more perfect crystalline structure of the graphitic carbon nitride product.Electrochemical characterizations show that the g-C3N4 has electrocatalytic activity toward ORR through a two-step and two-electron process.

  13. Calibration of the KARMEN detector and the analyses of inclusive neutrino reactions with 12C

    International Nuclear Information System (INIS)

    The KARMEN neutrino experiment is taking data at the spallation neutron source ISIS at the Rutherford Appleton Laboratory in England. Its major aims are the search for neutrino oscillations and the investigation of neutrino-induced excitation of nuclei. ISIS provides three different kinds of neutrinos from the π+ decay (νμ) and from the subsequent μ+ decay ( anti νμ,νe). About 99.96% of these charged particles are stopped within the target material before they are decaying. Therefore the neutrinos have well defined energies, determined by the kinematics of the decay at rest. The spectrum includes energies between 0 and 52.8 MeV. The KARMEN detector detects neutrino reactions with 65 m3 of a liquid organic scintillator. In addition the 12C nuclei of the scintillator are used as reaction partner for the observed neutrino nuclei excitation. This thesis includes two parts. The first part describes the calibration of the detector data. Between 1992 and 1994 the concept of the calibration has been completely reworked and newly conceived in large parts. It includes all data, which are mainly composed of energy, position and time signals. The second part investigates neutrino reactions with 12C using a single prong analysis. The evlauation was made with neutrinos from muon decay. It includes the neutral current excitation of the 12C(15.11 MeV) level by anti νμandνe as well as the inclusive charged current excitation to 12N by νe. The cross section of the neutral current excitation has been determined. (orig.)

  14. Practical Aspects of Carbon-Carbon Cross-Coupling Reactions Using Heteroarenes

    NARCIS (Netherlands)

    Slagt, Vincent F.; Vries, André H.M. de; Vries, Johannes G. de; Kellogg, Richard M.

    2010-01-01

    The use of cross-coupling reactions for the preparation of alkylated and arylated heteroaromatic compounds has increased tremendously over the past two decades. This has been driven on the one hand by the increasingly complex structures of new drugs, most of which contain one or more heterocyclic mo

  15. Synthesis of propylene carbonate from urea and propylene glycol over zinc oxide: A homogeneous reaction

    OpenAIRE

    Dengfeng Wang; Xuelan Zhang; Tingting Cheng; Jing Wu; Qijun Xue

    2014-01-01

    In this work, several metal oxides and zinc salts were used to catalyze propylene carbonate (PC) synthesis from urea and propylene glycol (PG). According to the results of catalytic test and characterization, the catalytic pattern of ZnO was different from that of other metal oxides such as CaO, MgO and La2O3, but similar to that of zinc salts. In fact, the leaching of Zn species took place during reaction for ZnO. And ZnO was found to be the precursor of homogenous catalyst for reaction of u...

  16. tert-Butanesulfinamides as Nitrogen Nucleophiles in Carbon-Nitrogen Bond Forming Reactions.

    Science.gov (United States)

    Ramirez Hernandez, Johana; Chemla, Fabrice; Ferreira, Franck; Jackowski, Olivier; Oble, Julie; Perez-Luna, Alejandro; Poli, Giovanni

    2016-01-01

    The use of tert-butanesulfinamides as nitrogen nucleophiles in carbon-nitrogen bond forming reactions is reviewed. This field has grown in the shadow of the general interest in N-tert-butanesulfinyl imines for asymmetric synthesis and occupies now an important place in its own right in the chemistry of the chiral amine reagent tert-butanesulfinamide. This article provides an overview of the area and emphasizes recent contributions wherein the tert-butanesulfinamides act as chiral auxiliaries or perform as nitrogen donors in metal-catalyzed amination reactions. PMID:26931222

  17. Incomplete fusion reactions: a comparison of 12,13C + 159Tb results

    International Nuclear Information System (INIS)

    In case of ICF reactions, besides the formation of a fusion-like nucleus, forward peaked fast α-particles have been observed. However, in recent years the unexpected influence of incomplete fusion over total fusion has been observed at low projectile energies. As such, a program has been undertaken to carry out some conclusive measurements using 13C, 14N and 18O beams on different targets, which may provide a rich data set to understand the underlying dynamics. The present work is the first step in this direction, where, the excitations functions of 12C + 159Tb and 13C + 159Tb (present work) systems at energies ≅ 4-7 MeV/A have been compared to study convincingly the effect of projectile on the reaction dynamics

  18. Velocity Map Imaging Study of Ion-Radical Chemistry: Charge Transfer and Carbon-Carbon Bond Formation in the Reactions of Allyl Radicals with C(.).

    Science.gov (United States)

    Pei, Linsen; Farrar, James M

    2016-08-11

    We present an experimental and computational study of the dynamics of collisions of ground state carbon cations with allyl radicals, C3H5, at a collision energy of 2.2 eV. Charge transfer to produce the allyl cation, C3H5(+), is exoergic by 3.08 eV and proceeds via energy resonance such that the electron transfer occurs without a significant change in nuclear velocities. The products have sufficient energy to undergo the dissociation process C3H5(+) → C3H4(+) + H. Approximately 80% of the reaction products are ascribed to charge transfer, with ∼40% of those products decaying via loss of a hydrogen atom. We also observe products arising from the formation of new carbon-carbon bonds. The experimental velocity space flux distributions for the four-carbon products are symmetric about the centroid of the reactants, providing direct evidence that the products are mediated by formation of a C4H5(+) complex living at least a few rotational periods. The primary four-carbon reaction products are formed by elimination of molecular hydrogen from the C4H5(+) complex. More than 75% of the nascent C4H3(+) products decay by C-H bond cleavage to yield a C4H2(+) species. Quantum chemical calculations at the MP2/6-311+g(d,p) level of theory support the formation of a nonplanar cyclic C4H5(+) adduct that is produced when the p-orbital containing the unpaired electron on C(+) overlaps with the unpaired spin density on the terminal carbon atoms in allyl. Product formation then occurs by 1,2-elimination of molecular hydrogen from the cyclic intermediate to form a planar cyclic C4H3(+) product. The large rearrangement in geometry as the C4H3(+) products are formed is consistent with high vibrational excitation in that product and supports the observation that the majority of those products decay to form the C4H2(+) species. PMID:27434380

  19. Investigating 13C +12C reaction by the activation method. Sensitivity tests

    Science.gov (United States)

    Chesneanu, Daniela; Trache, L.; Margineanu, R.; Pantelica, A.; Ghita, D.; Straticiuc, M.; Burducea, I.; Blebea-Apostu, A. M.; Gomoiu, C. M.; Tang, X.

    2015-02-01

    We have performed experiments to check the limits of sensitivity of the activation method using the new 3 MV Tandetron accelerator and the low and ultra-low background laboratories of the "Horia Hulubei" National Institute of Physics and Nuclear Engineering (IFIN-HH). We have used the 12C +13C reaction at beam energies Elab= 6, 7 and 8 MeV. The knowledge of this fusion cross section at deep sub-barrier energies is of interest for astrophysical applications, as it provides an upper limit for the fusion cross section of 12C +12C over a wide energy range. A 13C beam with intensities 0.5-2 particleμA was provided by the accelerator and used to bombard graphite targets, resulting in activation with 24Na from the 12C (13C ,p) reaction. The 1369 and 2754 keV gamma-rays from 24Na de-activation were clearly observed in the spectra obtained in two different laboratories used for measurements at low and ultralow background: one at the surface and one located underground in the Unirea salt mine from Slanic Prahova, Romania. In the underground laboratory, for Elab = 6 MeV we have measured an activity of 0.085 ± 0.011 Bq, corresponding to cross sections of 1-3 nb. This demonstrates that it is possible to measure 12C targets irradiated at lower energies for at least 10 times lower cross sections than before β-γ coincidences will lead us another factor of 10 lower, proving that this installations can be successfully used for nuclear astrophysics measurements.

  20. Determination of {sup 13}C/{sup 12}C ratios with (d, p) nuclear reactions

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Y.Q., E-mail: yqwang@lanl.go [Materials Science and Technology Division, Los Alamos National Laboratory, NM 87544 (United States); Zhang, J. [Materials Science and Technology Division, Los Alamos National Laboratory, NM 87544 (United States); School of Nuclear Science and Technology, Lanzhou University, Gansu 730000 (China); Tesmer, J.R. [Materials Science and Technology Division, Los Alamos National Laboratory, NM 87544 (United States); Li, Y.H. [Materials Science and Technology Division, Los Alamos National Laboratory, NM 87544 (United States); School of Nuclear Science and Technology, Lanzhou University, Gansu 730000 (China); Greco, R. [Materials Science and Technology Division, Los Alamos National Laboratory, NM 87544 (United States); Grim, G.P.; Obst, A.W. [Physics Division, Los Alamos National Laboratory, NM 87544 (United States); Rundberg, R.S.; Wilhelmy, J.B. [Chemistry Division, Los Alamos National Laboratory, NM 87544 (United States)

    2010-06-15

    Stable isotope ratios such as {sup 13}C/{sup 12}C play an important role in many applications including environment and energy research. Since many surface analysis techniques are plagued with unavoidable hydrocarbon contamination issues during analysis, it is highly desirable that {sup 13}C and {sup 12}C isotopes be measured simultaneously especially in specimens with a minute amount of {sup 13}C, in order to reliably determine {sup 13}C/{sup 12}C ratios. In this paper, we report that deuterium induced proton particle reactions, {sup 13}C(d, p){sup 14}C and {sup 12}C(d, p){sup 13}C, provide a convenient and reliable approach for {sup 13}C/{sup 12}C ratio determination. Optimizations on experimental considerations and potential interferences from other common light isotopes are discussed as well as results from the application of this technique to diagnose the performance of a target debris collection in an inertial confinement fusion (ICF) experiment.

  1. Reservoir-Condition Pore-Scale Imaging of Reaction in Carbonates using Synchrotron Fast Tomography

    Science.gov (United States)

    Menke, H. P.; Andrew, M. G.; Bijeljic, B.; Blunt, M. J.

    2015-12-01

    Carbon capture and storage in carbonate reservoirs is essential for mitigating climate change. Supercritical CO2 mixed with host brine is acidic and can dissolve the surrounding pore structure and change flow dynamics. However, the type, speed, and magnitude of the dissolution are dependent on both the reactive transport properties of the pore-fluid and the intrinsic properties of the rock. Understanding how changes in the pore structure, chemistry, and flow properties affect dissolution is vital for successful predictive modelling both on the pore-scale and for up-scaled reservoir simulations. Reaction in carbonates has been studied at the pore-scale but has never been imaged dynamically in situ. We present an experimental method whereby both lab-based benchtop instruments and 'Pink Beam' synchrotron radiation are used in X-ray microtomography to investigate pore structure changes during supercritical CO2 injection at reservoir conditions. Three types of pure limestone rock with broadly varying rock topology were imaged under the same reservoir conditions. Flow-rate and brine acidity was varied in successive experiments by half an order of magnitude to gain insight into the impact of flow, transport, and physical heterogeneity. The images were binarized and the magnitude of dissolution was identified on a voxel-by-voxel basis to extract pore-by-pore dissolution data. The impact of dissolution on flow characteristics was studied by computing the evolution of the pore-scale velocity fields with a flow solver. We found that increasing rock heterogeneity increased channelized flow [Figure 1] through preferential pathways and that higher flow rate increased total dissolution. Additionally, decreasing reaction rate lowered overall reaction rate and made axial flow less uniform. Experimentally measured reaction rates in real rocks are at least an order of magnitude lower when compared to batch experiments. We provide evidence that this can be due to transport limitations

  2. Heavy ion identification, complete fusion reaction 20Ne + 12C at 110 MeV

    International Nuclear Information System (INIS)

    Various means of complete evaporation residues identification (E, Z, A) are compared. The experimental set up described uses 'ΔE, magnetic rigidity, time of flight' method. Previsions of performances are confirmed. Isotopic distributions of evaporation residues in the 20Ne + 12C reaction plus energy and angular distributions are in good agreement with compound nucleus statistical model predictions. Ionic charge distributions of the residues between 1.5 MeV/a.m.u and 4 MeV/a.m.u are satisfactorily reproduced by a semi-empirical formula

  3. Cycloaddition Reaction of Carbon Dioxide to Epoxides Catalyzed by Polymer-Supported Quaternary Phosphonium Salts

    Directory of Open Access Journals (Sweden)

    Yubing Xiong

    2013-01-01

    Full Text Available Polymer-supported quaternary phosphonium salt (PS-QPS was explored as effective catalyst for the coupling reaction of carbon dioxide with epoxides. The results indicated that cyclic carbonates with high yields (98.6% and excellent selectivity (100% could be prepared at the conditions of 5 MPa CO2, 150°C, and 6 h without the addition of organic solvents or cocatalysts. The effects of various reaction conditions on the catalytic performance were investigated in detail. The catalyst is applicable to a variety of epoxides, producing the corresponding cyclic carbonates in good yields. Furthermore, the catalyst could be recovered easily and reused for five times without loss of catalytic activity obviously. A proposed mechanism for synthesis of cyclic carbonate in the presence of PS-QPS was discussed. The catalyst was characterized by thermogravimetric analysis (TGA, scanning electron microscopy (SEM, and Fourier transform infrared (FT-IR spectrum. It is believed that PS-QPS is of great potential for CO2 fixation applications due to its unusual advantages, such as easy preparation, high activity and selectivity, stability, low cost, and reusability.

  4. Use of 12C(d,p)13C and 16O(d,p)17O reactions

    International Nuclear Information System (INIS)

    The use of nuclear reactions for depth profiling carbon and oxygen in solids is discussed. A general expression for the yield from a nuclear reaction is derived and used to extract depth profiles from the energy spectra by two methods. The first method compares data from a target of unknown composition with a target containing a known concentration of either carbon or oxygen. By dividing the yields from the samples for equal collision energies, a concentration profile within the analyzed sample can be obtained. The second method uses published reaction cross section data to obtain the profile. The (d,p) profiling is demonstrated for carbon in ScD2. A comparison between the two methods is made by extracting carbon profiles in the near surface region of ScD2 samples. Effects due to inaccurate stopping cross section data are described. The technique is discussed for the 16O(d,p) reactions used to profile oxygen along with the effect of interferences from the 2H(d,p)3H reaction and other reactions

  5. Theoretical study of the P-Ylide reaction in the carbon nanotube

    Institute of Scientific and Technical Information of China (English)

    XIAO Bo; ZHAO JingXiang; DING YiHong; SUN ChiaChung

    2009-01-01

    Recent studies have shown that the inner phase of carbon nanotubes (CNTs) can not only change the properties of molecules inside the tube,but also enhance or restrain the S_N2 reactions.Thus,the CNTs can be considered a form of solid solvent.In this paper,we study the[2+2]cycloaddition reaction between CH_2O and PH_3CH_2 in the gas phase,benzene solution and inner phase of CNT using the density functional theory (DFT).The results indicate that the inner phase of CNT has little effect on the[2+2]cycloaddition reaction.This can be explained as that while taking the linear arrangement for S_N2 reaction,the reactants do not possess the axial symmetry for the studied[2+2]cycloaddition reaction.Therefore,although the CNT has large axial polarizability,it can exert little influence on the[2+2]cycloaddition reaction.Our studies will be helpful for further understanding of the inner phase chemistry of CNTs.

  6. RCNP E398 {sup 16}O,{sup 12}C(p,p’) experiment: Measurement of the γ-ray emission probability from giant resonances in relation to {sup 16}O,{sup 12}C(ν,ν’) reactions

    Energy Technology Data Exchange (ETDEWEB)

    Ou, I.; Yamada, Y.; Mori, T.; Yano, T.; Sakuda, M. [Department of Physics, Okayama University, Okayama 700-8530 (Japan); Tamii, A.; Suzuki, T.; Yosoi, M.; Aoi, N.; Ideguchi, E.; Hashimoto, T.; Miki, K.; Ito, T.; Iwamoto, C.; Yamamoto, T. [Research Center for Nuclear Physics (RCNP), Osaka University, Ibaraki, Osaka 567-0047 (Japan); Akimune, H. [Department of Physics, Konan University, Okamoto 8-9-1, Higashinada, Kobe 658-8501 (Japan)

    2015-05-15

    We propose to measure the γ-ray emission probability from excited states above 5 MeV including giant resonance of {sup 16}O and {sup 12}C as a function of excitation energy in 1-MeV step. Here, we measure both the excitation energy (E{sub x}=5-30MeV) at the forward scattering angles (0°-3°) of the {sup 16}O, {sup 12}C (p, p’) reaction using Grand-Raiden Spectrometer and the energy of γ-rays (E{sub γ}) using an array of NaI(Tl) counters. The purpose of the experiment is to provide the basic and important information not only for the γ-ray production from primary neutral-current neutrino-oxygen (-carbon) interactions but also for that from the secondary hadronic (neutron-oxygen and -carbon) interactions.

  7. RCNP E398 16O,12C(p,p’) experiment: Measurement of the γ-ray emission probability from giant resonances in relation to 16O,12C(ν,ν’) reactions

    International Nuclear Information System (INIS)

    We propose to measure the γ-ray emission probability from excited states above 5 MeV including giant resonance of 16O and 12C as a function of excitation energy in 1-MeV step. Here, we measure both the excitation energy (Ex=5-30MeV) at the forward scattering angles (0°-3°) of the 16O, 12C (p, p’) reaction using Grand-Raiden Spectrometer and the energy of γ-rays (Eγ) using an array of NaI(Tl) counters. The purpose of the experiment is to provide the basic and important information not only for the γ-ray production from primary neutral-current neutrino-oxygen (-carbon) interactions but also for that from the secondary hadronic (neutron-oxygen and -carbon) interactions

  8. One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction

    Science.gov (United States)

    Yang, Bo; Tao, Chuanye; Shao, Taofeng

    2016-01-01

    Summary A novel three-component reaction has been developed to assemble biologically and pharmaceutically important tetracyclic fused imidazo[1,2-a]pyridines in a one-pot fashion utilizing readily available 2-aminopyridines, isatins and isocyanides. The three-component coupling proceeds through the Groebke–Blackburn–Bienaymé reaction followed by a retro-aza-ene reaction and subsequent nucleophilic reaction of the in-situ generated imidazo[1,2-a]pyridines bearing an isocyanate functional group. PMID:27559401

  9. The neighboring effect of isosorbide and its epimers in their reactions with dimethyl carbonate

    Directory of Open Access Journals (Sweden)

    Fabio Aricò

    2014-10-01

    Full Text Available The reactions of isosorbide and its epimers, isomannide and isoidide, with dimethyl carbonate have been herein investigated as easy access to bio-based products by a free-halogen chemistry approach. Isosorbide and its epimers show a different reactivity in bimolecular nucleophilic substitution with dimethyl carbonate (DMC. Carboxymethylation reaction was carried out in the presence of DMC and a weak base resulting in the high-yielding synthesis of dicarboxymethyl derivatives. Isomannide was the most reactive anydro sugar due to the less sterically hindered exo position of the OH groups. On the other hand, methylation of isosorbide and its epimers, conducted in the presence of a strong base and DMC, showed the higher reactivity of the endo hydroxyl group, isoidide being the most reactive epimer. This result has been ascribed to the neighboring effect due to the combination of the oxygen in β-position and the intramolecular hydrogen bond within the anhydro sugar structure. Methylation reactions were also conducted in autoclave at high temperature with the amphoteric catalyst hydrotalcite using DMC as reagent and solvent. In this case, the reactivity of the epimers resulted quite differently with isosorbide being the most reactive reagent possibly as a result of the structure of hydrotalcite comprising of both acidic and basic sites. The neighboring effect was observed with good evidence in these methylation reactions.

  10. Mechanism of ({sup 14}N, {sup 12}B) reactions at intermediate energy leading to large spin-polarization of {sup 12}B

    Energy Technology Data Exchange (ETDEWEB)

    Mitsuoka, Shin-ichi [Osaka Univ., Ibaraki (Japan). Research Center for Nuclear Physics; Shimoda, Tadashi; Miyatake, Hiroari [and others

    1996-05-01

    To study mechanisms of the ({sup 14}N, {sup 12}B) reactions at intermediate energies, double differential cross section and nuclear spin-polarization of the {sup 12}B projectile-like fragments have been measured as a function of longitudinal momentum in the angular range of 0deg - 9deg. Large spin-polarization of the reaction products {sup 12}B has been observed in the {sup 9}Be({sup 14}N, {sup 12}B) reaction at 39.3 MeV/u. The momentum distributions at forward angles exhibit characteristic features which can not be understood by the current projectile fragmentation picture. It is shown that by assuming the existence of direct two-proton transfer process in addition to the fragmentation process, both the cross section and polarization of {sup 12}B fragments are successfully explained. The target and incident energy dependence of the momentum distribution are also explained reasonably. (author)

  11. Synthesis of propylene carbonate from urea and propylene glycol over zinc oxide: A homogeneous reaction

    Directory of Open Access Journals (Sweden)

    Dengfeng Wang

    2014-11-01

    Full Text Available In this work, several metal oxides and zinc salts were used to catalyze propylene carbonate (PC synthesis from urea and propylene glycol (PG. According to the results of catalytic test and characterization, the catalytic pattern of ZnO was different from that of other metal oxides such as CaO, MgO and La2O3, but similar to that of zinc salts. In fact, the leaching of Zn species took place during reaction for ZnO. And ZnO was found to be the precursor of homogenous catalyst for reaction of urea and PG. Thus, the relationship between the amount of dissolved zinc species and the catalytic performance of employed ZnO was revealed. In addition, a possible reaction mechanism over ZnO was discussed based on the catalytic runs and the characterization of XRD, FTIR, and element analysis.

  12. Effect of carbon on the Ni catalyzed methane cracking reaction: A DFT study

    Energy Technology Data Exchange (ETDEWEB)

    Li, Jingde; Croiset, Eric; Ricardez–Sandoval, Luis, E-mail: laricard@uwaterloo.ca

    2014-08-30

    Highlights: • Effect of carbon deposition on kinetic properties of methane dissociation is studied. • Existence of surface and subsurface C atoms destabilized CH{sub x} species adsorption. • CH{sub x} activation is hindered with the deposition of C on and in the Ni (1 1 1) surface. - Abstract: To understand the effects of carbon atoms on the Ni catalyzed methane cracking reactions, methane dissociation on clean, surface-carbon-covered, and subsurface-carbon-accumulated Ni(1 1 1) surfaces were investigated using density functional theory (DFT). The results show that the existence of surface and subsurface C atoms destabilized the adsorption of the surface hydrocarbon species when compared to the clean Ni(1 1 1) surface. The projected density state (PDOS) analysis shows that the deposition of C atoms on and into the Ni surface modified the electronic structure of the Ni surface, and thus reduced the catalytic activity of the bonded Ni atoms. Moreover, it was found that the presence carbon atoms increase the CH{sub x} (x = 4–1) species activation barriers especially on the surface carbon covered (1/4 ML) Ni(1 1 1) surface, where CH{sub x} (x = 4–1) species encounter highest energy barrier for dissociation due to the electronic deactivation induced by C-Ni bonding and the strong repulsive carbon -CH{sub x} interaction. The calculations also show that CH{sub x} dissociation barriers are not affected by its neighboring C atom at low surface carbon coverage (1/9 ML). This work can be used to estimate more realistic kinetic parameters for this system.

  13. The microscopic folding potential describing elastic scattering and astrophysical S factor of 12C + 12C fusion reaction at low energies

    International Nuclear Information System (INIS)

    The 12C + 12C reaction is important to understand the nuclear burning in stellar evolution. In this work, we calculate the 12C + 12C microscopic potential based on the effective nucleon-nucleon (NN) interaction and the wave functions of interaction nuclei. The Optical Model analysis for elastic scattering angular distributions of 12C + 12C system at energies near to the Coulomb barrier agrees well with the experimental data, which makes sure the applicability of our obtained potential. The Barrier Penetration Model (BPM) and WKB approximation are applied to estimate the astrophysical S factor, which is reasonable to measurement results. (author)

  14. Reaction dynamics of {sup 34-38}Mg projectile with carbon target using Glauber model

    Energy Technology Data Exchange (ETDEWEB)

    Shama, Mahesh K., E-mail: maheshphy82@gmail.com [School of Physics and Material Sciences, Thapar University Patiala-147004 (India); Department of Applied Sciences, Chandigarh Engineering College, Landran Mohali-140307 (India); Panda, R. N. [Department of Physics, ITER, Shiksha O Anusandhan University, Bhubaneswar-751030 (India); Sharma, Manoj K. [School of Physics and Material Sciences, Thapar University Patiala-147004 (India); Patra, S. K. [Institute of Physics, Sachivalaya marg Bhubneswar-751005 (India)

    2015-08-28

    We have studied nuclear reaction cross-sections for {sup 34-38}Mg isotopes as projectile with {sup 12}C target at projectile energy 240AMeV using Glauber model with the conjunction of densities from relativistic mean filed formalism. We found good agreement with the available experimental data. The halo status of {sup 37}Mg is also investigated.

  15. Thermodynamic Data for Geochemical Modeling of Carbonate Reactions Associated with CO2 Sequestration – Literature Review

    Energy Technology Data Exchange (ETDEWEB)

    Krupka, Kenneth M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Cantrell, Kirk J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); McGrail, B. Peter [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2010-09-01

    Permanent storage of anthropogenic CO2 in deep geologic formations is being considered as a means to reduce the concentration of atmospheric CO2 and thus its contribution to global climate change. To ensure safe and effective geologic sequestration, numerous studies have been completed of the extent to which the CO2 migrates within geologic formations and what physical and geochemical changes occur in these formations when CO2 is injected. Sophisticated, computerized reservoir simulations are used as part of field site and laboratory CO2 sequestration studies. These simulations use coupled multiphase flow-reactive chemical transport models and/or standalone (i.e., no coupled fluid transport) geochemical models to calculate gas solubility, aqueous complexation, reduction/oxidation (redox), and/or mineral solubility reactions related to CO2 injection and sequestration. Thermodynamic data are critical inputs to modeling geochemical processes. The adequacy of thermodynamic data for carbonate compounds has been identified as an important data requirement for the successful application of these geochemical reaction models to CO2 sequestration. A review of thermodynamic data for CO2 gas and carbonate aqueous species and minerals present in published data compilations and databases used in geochemical reaction models was therefore completed. Published studies that describe mineralogical analyses from CO2 sequestration field and natural analogue sites and laboratory studies were also reviewed to identify specific carbonate minerals that are important to CO2 sequestration reactions and therefore require thermodynamic data. The results of the literature review indicated that an extensive thermodynamic database exists for CO2 and CH4 gases, carbonate aqueous species, and carbonate minerals. Values of ΔfG298° and/or log Kr,298° are available for essentially all of these compounds. However, log Kr,T° or heat capacity values at temperatures above 298 K exist for less than

  16. Resonance strengths in the 14N(p,gamma)15O and 15N(p,alpha gamma)12C reactions

    CERN Document Server

    Marta, Michele; Bemmerer, Daniel; Beyer, Roland; Broggini, Carlo; Caciolli, Antonio; Erhard, Martin; Fülöp, Zsolt; Grosse, Eckart; Gyürky, György; Hannaske, Roland; Junghans, Arnd R; Menegazzo, Roberto; Nair, Chithra; Schwengner, Ronald; Szücs, Tamás; Vezzú, Simone; Wagner, Andreas; Yakorev, Dmitry

    2010-01-01

    The 14N(p,gamma)15O reaction is the slowest reaction of the carbon-nitrogen-oxygen cycle of hydrogen burning in stars. As a consequence, it determines the rate of the cycle. The 15N(p,alpha gamma)12C reaction is frequently used in inverse kinematics for hydrogen depth profiling in materials. The 14N(p,gamma)15O and 15N(p,alpha gamma)12C reactions have been studied simultaneously, using titanium nitride targets of natural isotopic composition and a proton beam. The strengths of the resonances at Ep = 1058 keV in 14N(p,gamma)15O and at Ep = 897 and 430 keV in 15N(p,alpha gamma)12C have been determined with improved precision, relative to the well-known resonance at Ep = 278 keV in 14N(p,gamma)15O. The new recommended values are \\omega\\gamma = 0.352$\\pm$0.018, 362$\\pm$20, and 22.0$\\pm$0.9\\,eV for their respective strengths. In addition, the branching ratios for the decay of the Ep = 1058 keV resonance in 14N(p,gamma)15O have been redetermined. The data reported here should facilitate future studies of off-resona...

  17. Reaction behavior between the oxide film of LY12 aluminum alloy and the flux

    Institute of Scientific and Technical Information of China (English)

    薛松柏; 董健; 吕晓春; 顾文华

    2004-01-01

    In this paper, the brazing mechanism of LY12 aluminum alloy at middle range temperature was presented. The CsF-AlF3 non-corrosive flux was utilized to remove the complex oxide film on the surface of LY12 aluminum alloy. The results revealed that the oxide film was removed by the improved CsF-AlF3 flux accompanied with the occurrence of reaction as well as dissolution and the compounds CsF played an important role to remove the oxide film. Actually, the high activity of flux, say, the ability to remove the oxide film, was due to the presence of the compounds, such as NH4F,NH4AlF4 and composite molten salt. The production of HF was the key issue to accelerate the reaction and enhance to eliminate the oxide film by dissolution. It was found that the rare earth element La at small percentage was not enriched at the interface. Moreover, the rare earth fluoride enhanced the dissolution behavior.

  18. Polyaniline-Derived Ordered Mesoporous Carbon as an Efficient Electrocatalyst for Oxygen Reduction Reaction

    Directory of Open Access Journals (Sweden)

    Kai Wan

    2015-06-01

    Full Text Available Nitrogen-doped ordered mesoporous carbon was synthesized by using polyaniline as the carbon source and SBA-15 as the template. The microstructure, composition and electrochemical behavior were extensively investigated by the nitrogen sorption isotherm, X-ray photoelectron spectroscopy, cyclic voltammetry and rotating ring-disk electrode. It is found that the pyrolysis temperature yielded a considerable effect on the pore structure, elemental composition and chemical configuration. The pyrolysis temperature from 800 to 1100 °C yielded a volcano-shape relationship with both the specific surface area and the content of the nitrogen-activated carbon. Electrochemical tests showed that the electrocatalytic activity followed a similar volcano-shape relationship, and the carbon catalyst synthesized at 1000 °C yielded the best performance. The post-treatment in NH3 was found to further increase the specific surface area and to enhance the nitrogen doping, especially the edge-type nitrogen, which favored the oxygen reduction reaction in both acid and alkaline media. The above findings shed light on electrocatalysis and offer more strategies for the controllable synthesis of the doped carbon catalyst.

  19. Experimental resolution of deuterium and hydrogen depth profiling with the nuclear reactions D(3He,p)α and p(15N,α,γ)12C

    International Nuclear Information System (INIS)

    In this paper well defined test samples are used to show how the analysis depth and the matrix material influence the depth resolution of nuclear reaction analysis. The reaction D(3He,p)α is used to detect deuterium. By covering 10 nm thin deuterated amorphous carbon (a–C:D) films on silicon with tungsten (ZW = 74) and titanium (ZTi = 22) of various thicknesses between 500 nm and 8 μm the influence of the atomic number and the overlayer thickness on the depth resolution is studied. The most probable depth profiles are calculated from the experimental data with the program NRADC, which implements Bayesian statistics. The resulting apparent layer width of the deuterium containing layer broadens with increasing thickness of the coating and this broadening is more pronounced for coatings with higher Z. These apparent layer widths are a measure for the experimentally achievable depth resolution. Their absolute values are in the same range as the theoretical optimum calculated with RESOLNRA. To investigate the depth resolution of the p(15N,α,γ)12C reaction, a 12 nm thin hydrogenated amorphous carbon (a–C:H) film on silicon and a pure tungsten sample are analysed. The width of the instrument function of this method is deduced from the surface hydrogen peak of the pure tungsten sample. The two methods are compared

  20. A Theoretical Investigation on the Reaction Mechanism of the C9H+ 12·Side-chain Decomposition

    Institute of Scientific and Technical Information of China (English)

    CHENG,Xueli; ZHAO,Yanyun; LI,Feng; ZHANG,Dongsheng

    2009-01-01

    n-Phenylpropane cation C9H+·12 serves as a prototype to investigate the reaction mechanisms of alkylbenzene cations.The decomposition reactions of C9H+·12 system have been studied extensively at the B3LYP/6-311 + + G**level with Gaussian 98 program package.All reaction channels were fully investigated with the vibrational mode analysis to confirm the transition states and with electron population analysis to discuss the electron redistribution,and to elucidate the reaction mechanism.The reaction mechanism shows that there is a non-barrier channel of C9H+·12→C7H+7+C2H·5,which is thermodynamically most favorable.

  1. Clustering effect of {sup 12}C fragmentation in p+{sup 12}C, {alpha}+{sup 12}C and {sup 14}N+{sup 12}C reactions

    Energy Technology Data Exchange (ETDEWEB)

    Takemoto, Hiroki; Horiuchi, Hisashi [Kyoto Univ. (Japan). Dept. of Physics; Ono, Akira

    1997-05-01

    In general, self-conjugate 4n-nuclei have anomalous excited states with the excitation energy 10-15 MeV, which are recognized to be generated by the change of the structure from the shell-model-like one into the cluster one due to the activation of the clustering degrees of freedom. In AMD (Antisymmetrized Molecular Dynamics) fermic nature of nucleons is treated exactly, because the wave function of A-body system is antisymmetrized by a Slater determinant. Hence Pauli principle has been fully incorporated in AMD. As a result, it was concluded that the features of {sup 12}C fragmentation are originated from the activation of alpha-cluster degrees of freedom by indicating the excitation energy spectra of {sup 12}C before its breakup at the dynamical stage. Excitation energy spectrum before {sup 12}C breakup into any fragments consists of two components. One distributes in the range 7-15 MeV and the other in the range above 15 MeV. Accordingly, the features is related to those excited states excited states of {sup 12}C that is considered to have the cluster structure. (G.K.)

  2. Integral measurement of the {sup 12}C(n, p){sup 12}B reaction up to 10 GeV

    Energy Technology Data Exchange (ETDEWEB)

    Zugec, P.; Bosnar, D. [University of Zagreb, Department of Physics, Faculty of Science, Zagreb (Croatia); Colonna, N.; Barbagallo, M.; Mastromarco, M.; Tagliente, G.; Variale, V. [Istituto Nazionale di Fisica Nucleare, Bari (Italy); Ventura, A. [Istituto Nazionale di Fisica Nucleare, Bologna (Italy); Mengoni, A. [ENEA, Bologna (Italy); Altstadt, S.; Langer, C.; Lederer, C.; Reifarth, R.; Schmidt, S.; Weigand, M. [Johann-Wolfgang-Goethe Universitaet, Frankfurt (Germany); Andrzejewski, J.; Marganiec, J.; Perkowski, J. [Uniwersytet Lodzki, Lodz (Poland); Audouin, L.; Leong, L.S.; Tassan-Got, L. [Centre National de la Recherche Scientifique/IN2P3 - IPN, Orsay (France); Becares, V.; Cano-Ott, D.; Garcia, A.R.; Gonzalez-Romero, E.; Martinez, T.; Mendoza, E. [Centro de Investigaciones Energeticas Medioambientales y Tecnologicas (CIEMAT), Madrid (Spain); Becvar, F.; Krticka, M.; Kroll, J.; Valenta, S. [Charles University, Prague (Czech Republic); Belloni, F.; Mondalaers, W.; Plompen, A.; Schillebeeckx, P. [European Commission JRC, Institute for Reference Materials and Measurements, Geel (Belgium); Berthoumieux, E.; Fraval, K.; Gunsing, F. [CEA/Saclay - IRFU, Gif-sur-Yvette (France); Billowes, J.; Ware, T.; Wright, T. [University of Manchester, Manchester (United Kingdom); Boccone, V.; Brugger, M.; Calviani, M.; Cerutti, F.; Chiaveri, E.; Chin, M.; Ferrari, A.; Guerrero, C.; Losito, R.; Roman, F.; Rubbia, C.; Tsinganis, A.; Versaci, R.; Vlachoudis, V.; Weiss, C. [CERN, Geneva (Switzerland); Calvino, F.; Cortes, G.; Gomez-Hornillos, M.B.; Riego, A. [Universitat Politecnica de Catalunya, Barcelona (Spain); Carrapico, C.; Goncalves, I.F.; Sarmento, R.; Vaz, P. [Universidade de Lisboa, C2TN-Instituto Superior Tecnico, Lisboa (Portugal); Cortes-Giraldo, M.A.; Praena, J.; Quesada, J. [Universidad de Sevilla, Sevilla (Spain); Cosentino, L.; Finocchiaro, P. [INFN - Laboratori Nazionali del Sud, Catania (Italy); Diakaki, M.; Karadimos, D.; Kokkoris, M.; Vlastou, R. [National Technical University of Athens (NTUA), Athens (Greece); Domingo-Pardo, C.; Giubrone, G.; Tain, J.L. [CSIC-Universidad de Valencia, Instituto de Fisica Corpuscular, Valencia (Spain); Dressler, R.; Heinitz, S.; Kivel, N.; Schumann, D. [Paul Scherrer Institut, Villigen (Switzerland); Duran, I.; Tarrio, D. [Universidade de Santiago de Compostela, Santiago de Compostela (Spain); Eleftheriadis, C.; Manousos, A. [Aristotle University of Thessaloniki, Thessaloniki (Greece); Ganesan, S.; Gurusamy, P.; Saxena, A. [Bhabha Atomic Research Centre (BARC), Mumbai (India); Griesmayer, E.; Jericha, E.; Leeb, H. [Atominstitut der Oesterreichischen Universitaeten, Technische Universitaet Wien, Wien (Austria); Jenkins, D.G.; Vermeulen, M.J. [University of York, York, Heslington (United Kingdom); Kaeppeler, F. [Karlsruhe Institute of Technology (KIT), Institut fuer Kernphysik, Karlsruhe (Germany); Lo Meo, S. [Istituto Nazionale di Fisica Nucleare, Bologna (Italy); ENEA, Bologna (Italy); Massimi, C.; Mingrone, F.; Vannini, G. [Dipartimento di Fisica, Universita di Bologna (IT); INFN, Bologna (IT); Mastinu, P. [Laboratori Nazionali di Legnaro, Istituto Nazionale di Fisica Nucleare, Legnaro (IT); Milazzo, P.M. [Istituto Nazionale di Fisica Nucleare, Trieste (IT); Mirea, M. [Horia Hulubei National Institute of Physics and Nuclear Engineering - IFIN HH, Magurele (RO); Musumarra, A. [Universita di Catania, Dipartimento di Fisica e Astronomia DFA, Catania (IT); INFN-Laboratori Nazionali del Sud, Catania (IT); Paradela, C. [European Commission JRC, Institute for Reference Materials and Measurements, Geel (BE); Universidade de Santiago de Compostela, Santiago de Compostela (ES); Pavlik, A. [Faculty of Physics, University of Vienna, Wien (AT); Rauscher, T. [University of Hertfordshire, Centre for Astrophysics Research, School of Physics, Astronomy and Mathematics, Hatfield (GB); University of Basel, Department of Physics, Basel (CH); Wallner, A. [Faculty of Physics, University of Vienna, Wien (AT); Australian National University, Research School of Physics and Engineering, Canberra (AU)

    2016-04-15

    The integral measurement of the {sup 12}C(n, p){sup 12}B reaction was performed at the neutron time-of-flight facility nTOF at CERN. The total number of {sup 12}B nuclei produced per neutron pulse of the nTOF beam was determined using the activation technique in combination with a time-of-flight technique. The cross section is integrated over the nTOF neutron energy spectrum from reaction threshold at 13.6 MeV to 10 GeV. Having been measured up to 1GeV on basis of the {sup 235}U(n, f) reaction, the neutron energy spectrum above 200 MeV has been re-evaluated due to the recent extension of the cross section reference for this particular reaction, which is otherwise considered a standard up to 200 MeV. The results from the dedicated GEANT4 simulations have been used to evaluate the neutron flux from 1 GeV up to 10 GeV. The experimental results related to the {sup 12}C(n, p){sup 12}B reaction are compared with the evaluated cross sections from major libraries and with the predictions of different GEANT4 models, which mostly underestimate the {sup 12}B production. On the contrary, a good reproduction of the integral cross section derived from measurements is obtained with TALYS-1.6 calculations, with optimized parameters. (orig.)

  3. Electrocatalytic Activity of Carbonized Nanostructured Polyanilines for Oxidation Reactions: Sensing of Nitrite Ions and Ascorbic Acid

    International Nuclear Information System (INIS)

    Highlights: • Carbonized PANIs prepared from various nanostructured PANI precursors • Electroanalytical performances of carbonized PANIs evaluated using voltammetry • Study of carbonized PANIs physico-chemical properties related to electroactivity • The lowest over-potential for NO2− oxidation at c-PANI (+0.87 V vs. SCE) • The lowest over-potential for ascorbic acid oxidation at both c-PANI and c-PANI-SSA - Abstract: A comparative study of the electrocatalytic activity of nitrogen-containing carbon nanomaterials, prepared by the carbonization of nanostructured polyaniline (PANI) salts, for the electrooxidation reactions is presented. Nanostructured PANI salts were synthesized by the oxidative polymerization of aniline with ammonium peroxydisulfate in an aqueous solution in the presence of 5-sulfosalicylic acid (PANI-SSA), 3,5-dinitrosalicylic acid (PANI-DNSA) as well as without added acid (PANI), and subsequently carbonized to c-PANI-SSA, c-PANI-DNSA and c-PANI, respectively. Glassy carbon tip was modified with nanostructured c-PANIs and used for the investigation of sensing of nitrite and ascorbic acid in aqueous solutions as model analytes by linear sweep voltammetry. All three types of the investigated c-PANIs gave excellent response to the nitrite ions and ascorbic acid electrooxidation. The lowest peak potential for nitrite ion oxidation exhibited c-PANI (+0.87 V vs. SCE), and for ascorbic acid oxidation both c-PANI and c-PANI-SSA (ca. + 0.13 V vs. SCE). Electrochemical data were correlated with structural and textural data obtained by Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, elemental and nitrogen sorption analysis

  4. The influence of carbon surface chemistry on supported palladium nanoparticles in heterogeneous reactions.

    Science.gov (United States)

    Ding, Yuxiao; Zhang, Liyun; Wu, Kuang-Hsu; Feng, Zhenbao; Shi, Wen; Gao, Qiang; Zhang, Bingsen; Su, Dang Sheng

    2016-10-15

    The surface chemistry of nanocarbon support can tailor chemical properties of precious metal nanoparticle/nanocarbon hybrid catalyst in heterogeneous reactions. We report on modified reduced graphene oxide (rGO) support with ionic liquid-derived carbonaceous surface for palladium nanoparticle (Pd NPs) decoration and their actions in different heterogeneous reactions. The surface chemistry of support materials was characterized in detail, and the influence of which on the formation and distribution of metal particles was further investigated. Three different types of reactions including Suzuki-Miyaura coupling reaction, CO oxidation and phenol reduction were examined in terms of reactivity and selectivity. The roles of substituted nitrogen in graphitic lattice and grafted groups on the carbon surface were exploited. Nitrogen-doping can give rise to changes in electronic properties of supported metals, and the Lewis basicity of the doped nitrogen atoms can favor the adsorption of acidic reactants in phenol reduction. The grafted groups derived a negative impact to the Suzuki-Miyaura coupling reaction, due to the involvement of larger reactant molecules, despite that they could prevent significant sintering of Pd NPs in the CO oxidation. PMID:27442144

  5. Efficacy of supercritical carbon dioxide for nonthermal inactivation of Escherichia coli K12 in apple cider

    Science.gov (United States)

    This study evaluated the efficacy of a supercritical carbon dioxide (SCCO2) system with a gas-liquid porous metal contactor for eliminating Escherichia coli K12 in apple cider. Pasteurized, preservative-free apple cider was inoculated with E. coli K12 and processed using the SCCO2 system at CO2 conc...

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

    Science.gov (United States)

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

    2016-05-11

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

  7. Thin film solid-state reactions forming carbides as contact materials for carbon-containing semiconductors

    Science.gov (United States)

    Leroy, W. P.; Detavernier, C.; Van Meirhaeghe, R. L.; Lavoie, C.

    2007-03-01

    Metal carbides are good candidates to contact carbon-based semiconductors (SiC, diamond, and carbon nanotubes). Here, we report on an in situ study of carbide formation during the solid-state reaction between thin films. The solid-state reaction was examined between 11 transition metals (W, Mo, Fe, Cr, V, Nb, Mn, Ti, Ta, Zr, and Hf) and an amorphous carbon layer. Capping layers (C or TiN) of different thicknesses were applied to prevent oxidation. Carbide formation is evidenced for nine metals and the phases formed have been identified (for a temperature ranging from 100to1100°C). W first forms W2C and then WC; Mo forms Mo2C; Fe forms Fe3C; Cr first forms metastable phases Cr2C and Cr3C2-x, and finally forms Cr3C2; V forms VCx; Nb transforms into Nb2C followed by NbC; Ti forms TiC; Ta first forms Ta2C and then TaC; and Hf transforms into HfC. The activation energy for the formation of the various carbide phases has been obtained by in situ x-ray diffraction.

  8. 16,20,21,23O-12C reaction cross sections at 1 GeV/nucleon

    International Nuclear Information System (INIS)

    In the present work, we analyze the reaction cross sections of 16,20,21,23O-12C at 1 GeV/nucleon within the framework of conventional Glauber theory. We analyze the reaction cross section of 16,20,21,23O from 12C at 1 GeV/nucleon using the uncorrelated part of the Glauber amplitude. The inputs needed in the theory are the elementary NN amplitude, and the density distributions for the colliding nuclei

  9. Metalloradical-Catalyzed Selective 1,2-Rh-H Insertion into the Aliphatic Carbon-Carbon Bond of Cyclooctane

    NARCIS (Netherlands)

    Y.W. Chan; B. de Bruin; K.S. Chan

    2015-01-01

    The selective aliphatic carboncarbon activation of cyclo-octane (c-octane) was achieved via the Rh-II(ttp)-catalyzed 1,2-addition of Rh(ttp)H to give Rh(ttp)(n-octyl) (ttp = tetratolylporphyrinato dianion) in good yield under mild reaction conditions. This mechanism is further supported by DFT calcu

  10. Mass Transfer and Reaction Kinetics in the Carbonization of Magnesium Oxide from Light Calcined Magnesia with Mechanical Force Enhancement

    Institute of Scientific and Technical Information of China (English)

    张焕军; 朱国才

    2004-01-01

    The carbonization of magnesium oxide particles by CO2 was investigated using a stirring mill reactor.The effects of the system temperature, stirring rotation speed, influx rate of CO2 and initial diameter of the magnesium oxide particles on the carbonization process were determined. The results show that the system temperature and the stirring rotation speed are the most significant influencing factors on the carbonization rate. The determination of critical decomposition temperature (CDT) gives the maximum carbonization rate with other conditions fixed. A theoretical model involving mass transfer and reaction kinetics was presented for the carbonization process.The apparent activation energy was calculated to be 32.8kJ·mo1-1. The carbonization process is co-controlled by diffusive mass transfer and chemical reaction. The model fits well with the experimental results.

  11. An Analysis of the $^{12}$C+$^{24}$Mg Reaction Using A New Coupling Potential

    CERN Document Server

    Boztosun, I

    2001-01-01

    We introduce a new coupling potential to explain the experimental data for the $^{12}$C+$^{24}$Mg system at numerous energies in the laboratory system from 16.0 MeV to 24.0 MeV. This new coupled-channels based approach involves replacing the usual first derivative coupling potential by a new, second-derivative coupling potential. This paper first shows and discusses the limitation of the standard coupled-channels theory in the case where one of the nuclei in the reaction is strongly deformed. Then, this new approach is shown to improve consistently the agreement with the experimental data and has made major improvement on all the previous coupled-channels calculations for this system.

  12. Reaction mechanism for the symmetric breakup of 24Mg following an interaction with 12C

    International Nuclear Information System (INIS)

    Data on the yield of the symmetric breakup of 24Mg as a function of beam energy are presented and compared with detailed calculations of the energy dependence. The 24Mg states seen in symmetric breakup agree with previously observed breakup states having spin and parities Jπ=4+,(6+),8+. The data allow the variations of yield for indivual states to be judged, as the beam energy is varied. The variation in the yield of the 4+ states is compared in detail with calculations assuming several possible compound nuclear or direct reaction mechanisms. It is concluded that a massive (12C) transfer or a simple statistical compound process are unlikely mechanisms, but that each of several other mechanisms is consistent with the data. ((orig.))

  13. Deformation effects in the 28Si + 12C and 28Si + 28Si reactions

    Indian Academy of Sciences (India)

    C Bhattacharya; M Rousseau; C Beck; V Rauch; R M Freeman; R Nouicer; F Haas; O Dorvaux; K Eddahbi; P Papka; O Stezwski; S Szilner; D Mahboub; A Szanto De Toledo; A Hachem; E Martin; S J Sanders

    2001-07-01

    The possible occurrence of highly deformed configurations is investigated in the 40Ca and 56Ni di-nuclear systems as formed in the 28Si + 12C, 28Si reactions by using the properties of emitted light charged particles. Inclusive as well as exclusive data of the heavy fragments and their associated light charged particles have been collected by using the ICARE charged particle multidetector array. The data are analysed by Monte Carlo CASCADE statistical-model calculations using a consistent set of parameters with spin-dependent level densities. Significant deformation effects at high spin are observed as well as an unexpected large 8Be cluster emission of a binary nature.

  14. Geometrical aspects of reaction cross sections for {sup 3}He, {sup 4}He and {sup 12}C projectiles

    Energy Technology Data Exchange (ETDEWEB)

    Ingemarsson, A. [Uppsala Univ. (Sweden). Dept. of Radiation Sciences; Lantz, M. [Uppsala Univ. (Sweden). The Svedberg Laboratory

    2003-04-01

    A black-disc model combined with accurate matter densities has been used for an investigation of reaction cross sections for {sup 3}He, {sup 4}He and {sup 12}C projectiles. A simple relation is derived between the energy dependence of the reaction cross sections and the strength of the nucleon-nucleon interaction. A comparison is also made of the reaction cross sections for {sup 3}He and {sup 4}He for six different nuclei {sup 12}C, {sup 16}O, {sup 40}Ca, {sup 58,60}Ni and {sup 208}Pb.

  15. Manufacture of Φ1.2m reaction bonded silicon carbide mirror blank CFID

    Science.gov (United States)

    Zhang, Ge; Zhao, Rucheng; Zhao, Wenxing; Bao, Jianxun

    2010-05-01

    Silicon carbide (SiC) is a new type candidate material for large-scale lightweight space mirror. Its low thermal distortion, high stiffness, fine optical quality and dimensional stability, make SiC an ideal material for large space born telescope. Since ten years Changchun institute optics, fine mechanics and physics (CIOMP) has developed reaction bonded SiC (RB-SiC) technology for space application, and can fabricate RB-SiC mirror with scale less than 1.0 meter for telescope. The green body is prepared with gel-casting method which is an attractive new ceramic forming process for making high-quality, complex-shaped ceramic parts. And then unmolding, drying, binder burning out, reacting bonded, the RB-SiC can be obtained. But with the development of space-born or ground telescope, the scale of primary mirror has exceeded 1.0 meter. So CIOMP has developed an assembly technique which called novel reaction-formed joint technology for larger RB-SiC mirror blank. The steps include joining of green bodies with mixture comprised of SiC particles and phenolic resin etc, firing, machining and sintering. Joining the Φ1.2 meter RB-SiC mirror blank by the novel reaction-formed joint technology. And testing the welding layer's performance, the results show that the thickness of 54-77μm, the microstructure and thermal property can be comparable to the substrate and the mechanical property are excellent in bending strength of 307MPa.

  16. Comparative temporal analysis of multiwalled carbon nanotube oxidation reactions: Evaluating chemical modifications on true nanotube surface

    Science.gov (United States)

    Pacheco, Flávia G.; Cotta, Alexandre A. C.; Gorgulho, Honória F.; Santos, Adelina P.; Macedo, Waldemar A. A.; Furtado, Clascídia A.

    2015-12-01

    The influence of extensive purification on oxidized multiwalled carbon nanotube surface composition was studied through the characterization and differentiation of the actual surface submitted to three oxidation methods: microwave-assisted acid oxidation, hydrogen peroxide reflux, and Fenton reaction. The oxidized samples were purified by a multi-step procedure including the sequential use of basic reflux and dispersion in dimethylformamide (DMF). The results showed a significant increase in the amount of oxidation debris with hydrogen peroxide and Fenton reaction times longer than 8 h and strong surface characteristic modification. With regard to sample purification, basic reflux led to a reduction in oxygenated group concentration of only 10% in the samples treated by acid oxidation. On the other hand, the subsequent use of DMF led to a further decrease in concentration of 39%, proving to be a more efficient method for the removal of oxidation debris.

  17. Dilepton spectroscopy at intermediate energies; the carbon - carbon reaction at 1 GeV/A; Spectroscopie des dileptons aux energies intermediaires; la reaction carbone - carbone A 1 GeV/A

    Energy Technology Data Exchange (ETDEWEB)

    Prunet, M.

    1995-06-01

    The Physics context of this work is heavy ion collisions at relativistic energies where di-electron provide informations on the produced hot and dense nuclear matter. The experiment is performed by the DiLepton Spectrometer (DLS) Collaboration at the Lawrence Berkeley`s Bevalac. After a description of the apparatus, we review the whole program and the main results so far obtained: first evidence of a significant di-electron signal at energies above 1 GeV/A; improvement of the understanding of di-electron production (electromagnetic decays of hadrons, {pi}{sup +}{pi}{sup -} annihilation and hadronic Bremsstrahlung). The results of p-p, p-d reactions from 1 to 4.9 GeV/A show that hadronic Bremsstrahlung (pp, pn) should be reformulated. Our analysis, optimized on the reaction Carbon-Carbon at 1 GeV/A, has been applied to {alpha}-Ca and d-Ca. We have developed two main aspects: improvement of the time resolution (500 ps) in order to eliminate all of the protons. Improvement of the space resolution (300 {mu}) for better mass resolution, in particular in the {rho} region. We obtain the cross section of di-electron production as a function of mass, transverse momentum and rapidity from the C-C, {alpha}-Ca and d-Ca reactions at 1 GeV/A. We also compare the cross section for all of the measured systems at 1 GeV/A, including Ca-Ca, and we show a (ApAt){sup {alpha}} dependence with {alpha} {approx_equal} 1.1. A study of the associated multiplicity has also been performed. Nevertheless, the limited acceptance of the DLS and its poor mass resolution to identify the {rho}, {omega} vector mesons, do not allow to conclude on hadron behaviour in nuclear matter. This point is one of the main goal of the HADES project at GSI (Darmstadt), which we give a brief description of the main features. (authors). 60 refs.

  18. Hetero-atom doped carbon nanotubes for dye degradation and oxygen reduction reaction

    Energy Technology Data Exchange (ETDEWEB)

    Nandan, Ravi, E-mail: aerawat27@gmail.com; Nanda, Karuna Kar [Materials Research Centre, Indian Institute of Science, Bangalore-560012 (India)

    2015-06-24

    We report the synthesis of nitrogen doped vertically aligned multi-walled (MWNCNTs) carbon nanotubes by pyrolysis and its catalytic performance for degradation of methylene blue (MB) dye & oxygen reduction reaction (ORR). The degradation of MB was monitored spectrophotometrically with time. Kinetic studies show the degradation of MB follows a first order kinetic with rate constant k=0.0178 min{sup −1}. The present rate constant is better than that reported for various supported/non-supported semiconducting nanomaterials. Further ORR performance in alkaline media makes MWNCNTs a promising cost-effective, fuel crossover tolerance, metal-free, eco-friendly cathode catalyst for direct alcohol fuel cell.

  19. Hetero-atom doped carbon nanotubes for dye degradation and oxygen reduction reaction

    International Nuclear Information System (INIS)

    We report the synthesis of nitrogen doped vertically aligned multi-walled (MWNCNTs) carbon nanotubes by pyrolysis and its catalytic performance for degradation of methylene blue (MB) dye & oxygen reduction reaction (ORR). The degradation of MB was monitored spectrophotometrically with time. Kinetic studies show the degradation of MB follows a first order kinetic with rate constant k=0.0178 min−1. The present rate constant is better than that reported for various supported/non-supported semiconducting nanomaterials. Further ORR performance in alkaline media makes MWNCNTs a promising cost-effective, fuel crossover tolerance, metal-free, eco-friendly cathode catalyst for direct alcohol fuel cell

  20. Stepwise Quenching of Exciton Fluorescence in Carbon Nanotubes by Single Molecule Reactions

    CERN Document Server

    Cognet, Laurent; Rocha, John-David R; Doyle, Condell D; Tour, James M; Weisman, R Bruce

    2007-01-01

    Single-molecule chemical reactions with individual single-walled carbon nanotubes were observed through near-infrared photoluminescence microscopy. The emission intensity within distinct submicrometer segments of single nanotubes changes in discrete steps after exposure to acid, base, or diazonium reactants. The steps are uncorrelated in space and time, and reflect the quenching of mobile excitons at localized sites of reversible or irreversible chemical attack. Analysis of step amplitudes reveals an exciton diffusional range of about 90 nanometers, independent of nanotube structure. Each exciton visits approximately 104 atomic sites during its lifetime, providing highly efficient sensing of local chemical and physical perturbations.

  1. Carbon-14 immobilization via the CO2-Ba(OH)2 hydrate gas-solid reaction

    International Nuclear Information System (INIS)

    Although no restrictions have been placed on the release of carbon-14, it has been identified as a potential health hazard due to the ease in which it may be assimilated into the biosphere. The intent of the Carbon-14 Immobilization Program, funded through the Airborne Waste Program Management Office, is to develop and demonstrate a novel process for restricting off-gas releases of carbon-14 from various nuclear facilities. The process utilizes the CO2-Ba(OH)2 hydrate gas-solid reaction to directly remove and immobilize carbon-14. The reaction product, BaCO3, possesses both the thermal and chemical stability desired for long-term waste disposal. The process is capable of providing decontamination factors in excess of 1000 and reactant utilization of greater than 99% in the treatment of high volumetric, airlike (330 ppM CO2) gas streams. For the treatment of an air-based off-gas stream, the use of packed beds of Ba(OH)2.8H2O flakes to remove CO2 has been demonstrated. However, the operating conditions must be maintained between certain upper and lower limits with respect to the partial pressure of water. If the water vapor pressure in the gas is less than the dissociation vapor pressure of Ba(OH)2.8H2O, the bed will deactivate. If the vapor pressure is considerably greater, pressure drop problems will increase with increasing humidity as the particles curl and degrade. Results have indicated that when operated in the proper regime, the bulk of the increase in pressure drop results from the conversion of Ba(OH)2.8H2O to BaCO3 and not from the hydration of the commercial Ba(OH)2.8H2O (i.e. Ba(OH)2.7.50H2O) to Ba(OH)2.8H2O

  2. Rapid Access to Spirocyclized Indolenines via Palladium-Catalyzed Cascade Reactions of Tryptamine Derivatives and Propargyl Carbonate

    OpenAIRE

    Montgomery, Thomas D.; Nibbs, Antoinette E.; Zhu, Ye; Rawal, Viresh H.

    2014-01-01

    We report the intermolecular palladium-catalyzed reaction of tert-butyl propargyl carbonate with tryptamine derivatives or other indole-containing bis-nucleophiles. The reaction proceeds under mild conditions and with low catalyst loadings to afford novel spiroindolenine products in good to high yields.

  3. Palladium on Carbon-Catalyzed Suzuki-Miyaura Coupling Reaction Using an Efficient and Continuous Flow System

    Directory of Open Access Journals (Sweden)

    Tomohiro Hattori

    2015-01-01

    Full Text Available The continuous flow Suzuki-Miyaura reaction between various haloarenes and arylboronic acids was successfully achieved within only ca. 20 s during the single-pass through a cartridge filled with palladium on carbon (Pd/C. No palladium leaching was observed in the collected reaction solution by atomic absorption spectrometry (detection limit: 1 ppm.

  4. Benzyl alcohol oxidation in supercritical carbon dioxide: spectroscopic insight into phase behaviour and reaction mechanism.

    Science.gov (United States)

    Caravati, Matteo; Grunwaldt, Jan-Dierk; Baiker, Alfons

    2005-01-21

    Selective oxidation of benzyl alcohol to benzaldehyde with molecular oxygen over an alumina-supported palladium catalyst was performed with high rate at about 95% selectivity in supercritical carbon dioxide. The experiments in a continuous flow fixed-bed reactor showed that the pressure has a strong influence on the reaction rate. A marked increase of the rate (turnover frequency) from 900 h(-1) to 1800 h(-1) was observed when increasing the pressure from 140 to 150 bar. Video monitoring of the bulk fluid phase behavior and the simultaneous investigation by transmission and attenuated total reflection (ATR) infrared spectroscopy at two positions of the view cell showed that the sharp increase in activity is correlated to a transition from a biphasic to a monophasic reaction mixture. In the single phase region, both oxygen and benzyl alcohol are dissolved in the supercritical CO2 phase, which leads to a reduction of the mass transport resistances (both in the external fluid film and in the catalyst pores) and thus to the high reaction rate measured in the catalytic experiments. The phase transition could be effectively and easily monitored by transmission and ATR-IR spectroscopy despite the small concentration of the dense liquid like phase. Deposition of the Pd/Al2O3 catalyst on the ATR-crystal at the bottom of the view cell allowed to gain insight into the chemical changes and mass transfer processes occurring in the solid/liquid interface region during reaction. Analyzing the shift of the upsilon2 bending mode of CO2 gave information on the fluid composition in and outside the catalyst pores. Moreover, the catalytic reaction could be investigated in situ in this spectroscopic batch reactor cell by monitoring simultaneously the reaction progress, the phase behaviour and the catalytic interface. PMID:19785149

  5. Theoretical and Experimental Study on Reaction Coupling: Dehydrogenation of Ethylbenzene in the Presence of Carbon Dioxide

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Dehydrogenation of ethylbenzene (EB) to styrene (ST) in the presence of CO2, in which EB dehydrogenation is coupled with the reverse water-gas shift (RWGS), was investigated extensively through both theoretical analysis and experimental characterization. The reaction coupling proved to be superior to the single dehydrogenation in several respects. Thermodynamic analysis suggests that equilibrium conversion of EB can be improved greatly by reaction coupling due to the simultaneous elimination of the hydrogen produced from dehydrogenation. Catalytic tests proved that iron and vanadium supported on activated carbon or Al2O3 with certain promoters are potential catalysts for this coupling process.The catalysts of iron and vanadium are different in the reaction mechanism, although ST yield is always associated with CO2 conversion over various catalysts. The two-step pathway plays an important role in the coupling process over Fe/Al2O3, while the one-step pathway dominates the reaction over V/Al2O3.Coke deposition and deep reduction of active components are the major causes of catalyst deactivation.CO2 can alleviate the catalyst deactivation effectively through preserving the active species at high valence in the coupling process, though it can not suppress the coke deposition.

  6. The reaction of carbon disulphide with -haloketones and primary amines in the presence of potassium iodide as catalyst

    Indian Academy of Sciences (India)

    Javad Safaei-Ghomi; Fariba Salimi; Ali Ramazani

    2013-09-01

    A simple, mild and convenient method has been developed for the synthesis of 3,4,5-trialkyl-1,3-thiazole-2(3)-thione derivatives through one pot three-component reaction between a primary amine, carbon disulphide, and -haloketone in the presence of potassium iodide at room temperature conditions. The products were obtained with excellent yield and appropriate reaction times. This reaction represents a rapid and unprecedented route to the described molecules that have biological specifications.

  7. Study of the 20,22Ne+20,22Ne and 10,12,13,14,15C+12C Fusion Reactions with MUSIC

    Directory of Open Access Journals (Sweden)

    Avila M. L.

    2016-01-01

    Full Text Available A highly efficient MUlti-Sampling Ionization Chamber (MUSIC detector has been developed for measurements of fusion reactions. A study of fusion cross sections in the 10,12,13,14,15C+12C and 20,22Ne+20,22Ne systems has been performed at ATLAS. Experimental results and comparison with theoretical predictions are presented. Furthermore, results of direct measurements of the 17O(α, n20Ne, 23Ne(α, p26Mg and 23Ne(α, n26Al reactions will be discussed.

  8. Study of the 20,22Ne+20,22Ne and 10,12,13,14,15C+12C Fusion Reactions with MUSIC

    Science.gov (United States)

    Avila, M. L.; Rehm, K. E.; Almaraz-Calderon, S.; Carnelli, P. F. F.; DiGiovine, B.; Esbensen, H.; Hoffman, C. R.; Jiang, C. L.; Kay, B. P.; Lai, J.; Nusair, O.; Pardo, R. C.; Santiago-Gonzalez, D.; Talwar, R.; Ugalde, C.

    2016-05-01

    A highly efficient MUlti-Sampling Ionization Chamber (MUSIC) detector has been developed for measurements of fusion reactions. A study of fusion cross sections in the 10,12,13,14,15C+12C and 20,22Ne+20,22Ne systems has been performed at ATLAS. Experimental results and comparison with theoretical predictions are presented. Furthermore, results of direct measurements of the 17O(α, n)20Ne, 23Ne(α, p)26Mg and 23Ne(α, n)26Al reactions will be discussed.

  9. Excited states in {sup 22}Mg via the {sup 12}C({sup 12}C, 2n){sup 22}Mg reaction

    Energy Technology Data Exchange (ETDEWEB)

    Jewett, C. [Department of Physics, Colorado School of Mines, Golden, CO (United States); Baktash, C. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Bardayan, D. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Blackmon, J. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Chipps, K. [Department of Physics, Colorado School of Mines, Golden, CO (United States); Galindo-Uribarri, A. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Greife, U. [Department of Physics, Colorado School of Mines, Golden, CO (United States)]. E-mail: ugreife@mines.edu; Gross, C. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Jones, K. [Department of Physics, Rutgers University, Piscataway, NJ (United States); Liang, F. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Livesay, J. [Department of Physics, Colorado School of Mines, Golden, CO (United States); Kozub, R. [Department of Physics, Tennessee Tech University, Cookeville, TN (United States); Nesaraja, C. [Department of Physics, Tennessee Tech University, Cookeville, TN (United States); Radford, D. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Sarazin, F. [Department of Physics, Colorado School of Mines, Golden, CO (United States); Smith, M.S. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Thomas, J. [Department of Physics, Rutgers University, Piscataway, NJ (United States); Yu, C.-H. [Physics Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States)

    2007-08-15

    The {sup 12}C({sup 12}C, 2n){sup 22}Mg reaction was measured with the CLARION array and the RMS separator at the Holifield Facility of Oak Ridge National Laboratory. This experiment was performed to gather more information on the excited states in {sup 22}Mg, which might be of relevance to recent radioactive ion beam measurements of the astrophysically important {sup 21}Na(p, {gamma}){sup 22}Mg reaction. The results are compared to direct measurements, transfer experiments and a competing experiment performed with Gammasphere.

  10. Effect of SiO2 on the Preparation and Properties of Pure Carbon Reaction Bonded Silicon Carbide Ceramics

    Institute of Scientific and Technical Information of China (English)

    WU Qi-de; GUO Bing-jian; YAN Yong-gao; ZHAO Xiu-jian; HONG Xiao-lin

    2004-01-01

    Effect of SiO2 content and sintering process on the composition and properties of Pure CarbonReaction Bonded Silicon Carbide (PCRBSC) ceramics prepared with C - SiO2 green body by infiltrating siliconwas presented. The infiltrating mechanism of C - SiO2 preform was also explored. The experimental results indicatethat the shaping pressure increases with the addition of SiO2 to the preform, and the pore size of the body turnedfiner and distributed in a narrower range, which is beneficial to decreasing the residual silicon content in the sin-tered materials and to avoiding shock off, thus increasing the conversion rate of SiC. SiO2 was deoxidized by car-bon at a high temperature and the gaseous SiO and CO produced are the main reason to the crack of the body atan elevated temperature. If the green body is deposited at 1800℃ in vacuum before infiltration crack will not beproduced in the preform and fully dense RBSC can be obtained. The ultimate material has the following properties:a density of3.05-3.12g/cm3 ,a strength of 580±32MPa and a hardness of (HRA)91-92.3.

  11. Hybrid capacitors utilizing halogen-based redox reactions at interface between carbon positive electrode and aqueous electrolytes

    Science.gov (United States)

    Yamazaki, Shigeaki; Ito, Tatsuya; Murakumo, Yuka; Naitou, Masashi; Shimooka, Toshiharu; Yamagata, Masaki; Ishikawa, Masashi

    2016-09-01

    We propose novel hybrid capacitors (HCs) with electrolyte-involved redox reactions of bromide or iodide species by pretreatment of an activated carbon positive electrode. The treatment is simple; impregnation of pores at an activated carbon fiber cloth (ACFC) as a positive electrode with bromine- or iodine-containing water before cell assembly. The treated positive electrode is applied to a HC cell with a non-treated negative electrode of ACFC and its electrochemical performance is investigated by galvanostatic cycling and leakage current tests. Few studies on such "electrolytic" charge storage systems have provided acceptable capacitor performance because of inevitable self-discharge caused by diffusion of charged species form an electrode to the other one through an electrolyte. Nevertheless, our electrolyte-redox-based HCs show excellent performance without undesirable diffusion of charged species. Moreover, the present HC utilizing a bromide redox system fulfills a practical cell voltage of 1.8 V in spite of an aqueous electrolyte system. This high voltage provides excellent energy density, which is 5 times higher than that in a conventional aqueous electric double-layer capacitor (EDLC), and 1.2 times higher even than that in a 2.7 V-class non-aqueous EDLC, while keeping high charge-discharge rate capability.

  12. Coprecipitation of (14)C and Sr with carbonate precipitates: The importance of reaction kinetics and recrystallization pathways.

    Science.gov (United States)

    Hodkin, David J; Stewart, Douglas I; Graham, James T; Burke, Ian T

    2016-08-15

    This study investigated the simultaneous removal of Sr(2+) and (14)CO3(2-) from pH>12 Ca(OH)2 solution by the precipitation of calcium carbonate. Initial Ca(2+):CO3(2-) ratios ranged from 10:1 to 10:100 (mM:mM). Maximum removal of (14)C and Sr(2+) both occurred in the system containing 10mM Ca(2+) and 1mM CO3(2-) (99.7% and 98.6% removal respectively). A kinetic model is provided that describes (14)C and Sr removal in terms of mineral dissolution and precipitation reactions. The removal of (14)C was achieved during the depletion of the initial TIC in solution, and was subsequently significantly affected by recrystallization of the calcite precipitate from an elongate to isotropic morphology. This liberated >46% of the (14)C back to solution. Sr(2+) removal occurred as Ca(2+) became depleted in solution and was not significantly affected by the recrystallization process. The proposed reaction could form the basis for low cost remediation scheme for (90)Sr and (14)C in radioactively contaminated waters (<$0.25 reagent cost per m(3) treated).

  13. Effect of denitrifying bacteria on the electrochemical reaction of activated carbon fiber in electrochemical biofilm system

    Institute of Scientific and Technical Information of China (English)

    YING Diwen; JIA Jinping; ZHANG Lehua

    2007-01-01

    An electrochemical-activated denitrifying biofilm system consisting of activated carbon fiber electrodes immobilized with denitrifying bacteria film as cathode was studied.A revised model for an electrochemical-activated denitrifying biofilm was developed and validated by electrochemical analysis of cathodal polarization curves and nitrate consumption rate.The cathodal polarization curve and nitrate consumption rate were introduced to verify the rate of electrochemical reaction and the activity of denitrifying bacteria,respectively.It was shown that the denitrification process effectively strengthened the electrochemical reaction while the electron also intensified denitrification activity.Electron was transferred between electrochemical process and biological process not only by hydrogen molecule but also by new produced active hydrogen atom.Additionally,a parameter of apparent exchange current density was deprived from the cathodal polarization curve with high overpotential,and a new bio-effect current density was defined through statistical analysis,which was linearly dependent to the activity of denitrification bacteria.Activated carbon fiber (ACF) electrode was also found to be more suitable to the electrochemical denitrifying system compared with graphite and platinum.

  14. The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity

    OpenAIRE

    Annamaria Deagostino; Cristina Prandi; Silvia Tabasso; Paolo Venturello

    2010-01-01

    This review is an overview of the last ten years’ use of the Mizoroki–Heck coupling applied to 1,2- and 1,3-dienes. Since both these systems form π-allyl palladium intermediates in Pd(0) coupling, they show particular chemical behavior. Many examples of 1,2-dienes Heck reactions are presented. 1,2-Dienes are important substrates because of their high reactivity that makes them useful building blocks for the synthesis of biologically relevant structures.

  15. Interfacial Cu+ promoted surface reactivity: Carbon monoxide oxidation reaction over polycrystalline copper-titania catalysts

    Science.gov (United States)

    Senanayake, Sanjaya D.; Pappoe, Naa Adokaley; Nguyen-Phan, Thuy-Duong; Luo, Si; Li, Yuanyuan; Xu, Wenqian; Liu, Zongyuan; Mudiyanselage, Kumudu; Johnston-Peck, Aaron C.; Frenkel, Anatoly I.; Heckler, Ilana; Stacchiola, Dario; Rodriguez, José A.

    2016-10-01

    We have studied the catalytic carbon monoxide (CO) oxidation (CO + 0.5O2 → CO2) reaction using a powder catalyst composed of both copper (5 wt.% loading) and titania (CuOx-TiO2). Our study was focused on revealing the role of Cu, and the interaction between Cu and TiO2, by systematic comparison between two nanocatalysts, CuOx-TiO2 and pure CuOx. We interrogated these catalysts under in situ conditions using X-ray diffraction (XRD), X-ray absorption fine structure (XAFS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) to probe the structure and electronic properties of the catalyst at all stages of the reaction and simultaneously probe the surface states or intermediates of this reaction. With the aid of several ex situ characterization techniques including transmission electron microscopy (TEM), the local catalyst morphology and structure were also studied. Our results show that a CuOx-TiO2 system is more active than bulk CuOx for the CO oxidation reaction due to its lower onset temperature and better stability at higher temperatures. Our results also suggest that surface Cu+ species observed in the CuOx-TiO2 interface are likely to be a key player in the CO oxidation mechanism, while implicating that the stabilization of this species is probably associated with the oxide-oxide interface. Both in situ DRIFTS and XAFS measurements reveal that there is likely to be a Cu(Ti)-O mixed oxide at this interface. We discuss the nature of this Cu(Ti)-O interface and interpret its role on the CO oxidation reaction.

  16. Gas-Phase Synthesis of Dimethyl Carbonate from Methanol and Carbon Dioxide Over Co1.5PW12O40 Keggin-Type Heteropolyanion

    Directory of Open Access Journals (Sweden)

    Ahmed Aouissi

    2010-03-01

    Full Text Available The reactivity of Co1.5PW12O40 in the direct synthesis of dimethyl carbonate (DMC from CO2 and CH3OH was investigated. The synthesized catalyst has been characterized by means of FTIR, XRD, TG, and DTA and tested in gas phase under atmospheric pressure. The effects of the reaction temperature, time on stream, and methanol weight hourly space velocity (MWHSV on the conversion and DMC selectivity were investigated. The highest conversion (7.6% and highest DMC selectivity (86.5% were obtained at the lowest temperature used (200 °C. Increasing the space velocity MWHSV increased the selectivity of DMC, but decreased the conversion. A gain of 18.4% of DMC selectivity was obtained when the MWHSV was increased from 0.65 h-1 to 3.2 h-1.

  17. Optical Potential Parameters for Halo Nucleus System 6He+12C from Transfer Reaction11B (7Li, 6He) 12C

    Institute of Scientific and Technical Information of China (English)

    WU Zhen-Dong; XU Xin-Xing; BAI Chun-Lin; YU Ning; JIA Fei; LIN Cheng-Jian; ZHANG Huan-Qiao; LIU Zu-Hua; YANG Feng; AN Guang-Peng; ZHANG Chun-Lei; ZHANG Gao-Long; JIA Hui-Ming

    2009-01-01

    The optical potential parameters for the halo nucleus system 6He+12 C are extracted from fits to the measured angular distributions of 11B(7 Li, 6He)12C reaction at energies of 18.3 and 28.3 MeV with distorted-wave Born approximation analysis. The characters of the obtained optical potential parameters are basically consistent with the results extracted from the fits to the elastic-scattering angular distributions in the literature.

  18. Heating Treated Carbon Nanotubes As Highly Active Electrocatalysts for Oxygen Reduction Reaction

    International Nuclear Information System (INIS)

    Graphical abstract: Heating treatment for multi-walled carbon nanotubes in the air introduces abundant structure defects which improve catalytic performances for oxygen reduction reaction (ORR). There is a positive correlation between the defect levels and ORR activities. The product shows better methanol tolerance and long-term durability than commercial Pt/C which makes it applicable in fuel cells. - Abstract: Carbon nanotubes (CNTs) have been widely developed for electrochemical energy conversion and storage devices for replacement of high-cost Pt-based catalysts. In this paper, a simple and convenient method is developed for improving the catalytic activity of CNTs in a controlled way. By simple heating treatment in the air, the multi-walled carbon nanotubes (MWCNTs) change with special morphologies, compositions and abundant defects (denoted as h-CNT). Those defects significantly improve the electrocatalytic performances for oxygen reduction reaction (ORR) which proceeds in a nearly four-electron pathway. The heating conditions have important effects on the structures and defect properties of h-CNTs which show a positive correlation between the defect levels and ORR performances. The small amounts of iron residues originated from nanotube growth and nitrogen doping during heating treatment also contribute to some catalytic activity. The inner walls of h-CNT remain intact during heating treatment and provide sufficient conductivity which facilitates charge transport during ORR. The h-CNT electrocatalyst shows better methanol tolerance and long-term durability than commercial Pt/C in alkaline media which makes it an alternative cathode catalyst in fuel cells

  19. Pyrolysis of Animal Bones with Vitamin B12: A Facile Route to Efficient Transition Metal-Nitrogen-Carbon (TM-N-C) Electrocatalysts for Oxygen Reduction.

    Science.gov (United States)

    Dou, Meiling; He, Duanpeng; Shao, Wenhao; Liu, Haijing; Wang, Feng; Dai, Liming

    2016-02-24

    By pyrolyzing cattle bones, hierarchical porous carbon (HPC) networks with a high surface area (2520 m(2)  g(-1) ) and connected pores were prepared at a low cost and large scale. Subsequent co-pyrolysis of HPC with vitamin B12 resulted in the formation of three-dimensional (3D) hierarchically structured porous cobalt-nitrogen-carbon (Co-N-HPC) electrocatalysts with a surface area as high as 859 m(2)  g(-1) as well as a higher oxygen reduction reaction (ORR) electrocatalytic activity, better operation stability, and higher tolerance to methanol than the commercial Pt/C catalyst in alkaline electrolyte.

  20. N-doped carbon nanomaterials are durable catalysts for oxygen reduction reaction in acidic fuel cells.

    Science.gov (United States)

    Shui, Jianglan; Wang, Min; Du, Feng; Dai, Liming

    2015-02-01

    The availability of low-cost, efficient, and durable catalysts for oxygen reduction reaction (ORR) is a prerequisite for commercialization of the fuel cell technology. Along with intensive research efforts of more than half a century in developing nonprecious metal catalysts (NPMCs) to replace the expensive and scarce platinum-based catalysts, a new class of carbon-based, low-cost, metal-free ORR catalysts was demonstrated to show superior ORR performance to commercial platinum catalysts, particularly in alkaline electrolytes. However, their large-scale practical application in more popular acidic polymer electrolyte membrane (PEM) fuel cells remained elusive because they are often found to be less effective in acidic electrolytes, and no attempt has been made for a single PEM cell test. We demonstrated that rationally designed, metal-free, nitrogen-doped carbon nanotubes and their graphene composites exhibited significantly better long-term operational stabilities and comparable gravimetric power densities with respect to the best NPMC in acidic PEM cells. This work represents a major breakthrough in removing the bottlenecks to translate low-cost, metal-free, carbon-based ORR catalysts to commercial reality, and opens avenues for clean energy generation from affordable and durable fuel cells.

  1. Cu,N-codoped Hierarchical Porous Carbons as Electrocatalysts for Oxygen Reduction Reaction.

    Science.gov (United States)

    Yu, Haiyan; Fisher, Adrian; Cheng, Daojian; Cao, Dapeng

    2016-08-24

    It remains a huge challenge to develop nonprecious electrocatalysts with high activity to substitute commercial Pt catalysts for oxygen reduction reactions (ORR). Here, the Cu,N-codoped hierarchical porous carbon (Cu-N-C) with a high content of pyridinic N was synthesized by carbonizing Cu-containing ZIF-8. Results indicate that Cu-N-C shows excellent ORR electrocatalyst properties. First of all, it nearly follows the four-electron route, and its electron transfer number reaches 3.92 at -0.4 V. Second, both the onset potential and limited current density of Cu-N-C are almost equal to those of a commercial Pt/C catalyst. Third, it exhibits a better half-wave potential (∼16 mV) than a commercial Pt/C catalyst. More importantly, the Cu-N-C displays better stability and methanol tolerance than the Pt/C catalyst. All of these good properties are attributed to hierarchical structure, high pyridinic N content, and the synergism of Cu and N dopants. The metal-N codoping strategy can significantly enhance the activity of electrocatalysts, and it will provide reference for the design of novel N-doped porous carbon ORR catalysts. PMID:27490846

  2. N-doped carbon nanomaterials are durable catalysts for oxygen reduction reaction in acidic fuel cells

    Science.gov (United States)

    Shui, Jianglan; Wang, Min; Du, Feng; Dai, Liming

    2015-01-01

    The availability of low-cost, efficient, and durable catalysts for oxygen reduction reaction (ORR) is a prerequisite for commercialization of the fuel cell technology. Along with intensive research efforts of more than half a century in developing nonprecious metal catalysts (NPMCs) to replace the expensive and scarce platinum-based catalysts, a new class of carbon-based, low-cost, metal-free ORR catalysts was demonstrated to show superior ORR performance to commercial platinum catalysts, particularly in alkaline electrolytes. However, their large-scale practical application in more popular acidic polymer electrolyte membrane (PEM) fuel cells remained elusive because they are often found to be less effective in acidic electrolytes, and no attempt has been made for a single PEM cell test. We demonstrated that rationally designed, metal-free, nitrogen-doped carbon nanotubes and their graphene composites exhibited significantly better long-term operational stabilities and comparable gravimetric power densities with respect to the best NPMC in acidic PEM cells. This work represents a major breakthrough in removing the bottlenecks to translate low-cost, metal-free, carbon-based ORR catalysts to commercial reality, and opens avenues for clean energy generation from affordable and durable fuel cells. PMID:26601132

  3. Cu,N-codoped Hierarchical Porous Carbons as Electrocatalysts for Oxygen Reduction Reaction.

    Science.gov (United States)

    Yu, Haiyan; Fisher, Adrian; Cheng, Daojian; Cao, Dapeng

    2016-08-24

    It remains a huge challenge to develop nonprecious electrocatalysts with high activity to substitute commercial Pt catalysts for oxygen reduction reactions (ORR). Here, the Cu,N-codoped hierarchical porous carbon (Cu-N-C) with a high content of pyridinic N was synthesized by carbonizing Cu-containing ZIF-8. Results indicate that Cu-N-C shows excellent ORR electrocatalyst properties. First of all, it nearly follows the four-electron route, and its electron transfer number reaches 3.92 at -0.4 V. Second, both the onset potential and limited current density of Cu-N-C are almost equal to those of a commercial Pt/C catalyst. Third, it exhibits a better half-wave potential (∼16 mV) than a commercial Pt/C catalyst. More importantly, the Cu-N-C displays better stability and methanol tolerance than the Pt/C catalyst. All of these good properties are attributed to hierarchical structure, high pyridinic N content, and the synergism of Cu and N dopants. The metal-N codoping strategy can significantly enhance the activity of electrocatalysts, and it will provide reference for the design of novel N-doped porous carbon ORR catalysts.

  4. The key role of metal dopants in nitrogen-doped carbon xerogel for oxygen reduction reaction

    Science.gov (United States)

    Liu, Sisi; Deng, Chengwei; Yao, Lan; Zhong, Hexiang; Zhang, Huamin

    2014-12-01

    Highly active non-precious metal catalysts based on nitrogen-doped carbon xerogel (NCX) for the oxygen reduction reaction (ORR) is prepared with resorcinol(R)-formaldehyde (F) resin as carbon precursor and NH3 as nitrogen source. NCX samples doped with various transition metal species are investigated to elucidate the effect of transition metals on the structure and ORR activity of the products. As-prepared NCX catalysts with different metals are characterized using nitrogen-adsorption analysis, X-ray diffractometry, X-ray photoelectron spectroscopy, and Raman spectroscopy. The structural properties and ORR activities of the catalysts are altered by addition of different metals, and NCX doped with iron exhibits the best ORR activity. Metal doping evidently promotes the formation of more micropores and mesopores. Raman and XPS studies reveal that iron, cobalt, and nickel can increase pyridinic-N contents and that iron can catalyse the formation of graphene structures and enhance quaternary-N contents. Whereas the total N-content does not determine ORR activity, Metal-N4/C-like species generated from the interaction of the metals with nitrogen and carbon atoms play important roles in achieving high ORR activity.

  5. Effect of Reaction Temperature on Carbon Yield and Morphology of CNTs on Copper Loaded Nickel Nanoparticles

    Directory of Open Access Journals (Sweden)

    Hu Ming

    2016-01-01

    Full Text Available This investigation was attempted to introduce carbon nanotubes (CNTs onto surface of copper powders in order to improve heat transfer performance of copper matrix for engineering application of electrical packaging materials. The Ni/MgO catalyst was formed on the copper powders surface by means of codeposition method. CVD technique was executed to fabricate uniform CNTs on copper powders and effect of reaction temperature on the morphology of CNTs was surveyed. The results showed that CNTs products on the copper powder surface were distributed uniformly even if reaction temperature was different. The diameter dimension of CNTs was within the scope of 30~60 nm. Growth behaviors of CNTs by CVD method were considered to be “tip-growth” mechanism. Raman spectra of CNTs proved that intensity ratio of D-band to G-band (ID/IG increased as deposition reaction temperature increased, which implied that order degree of graphitic structure in synthesized CNTs improved.

  6. Revealing Brown Carbon Chromophores Produced in Reactions of Methylglyoxal with Ammonium Sulfate

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Peng; Laskin, Julia; Nizkorodov, Sergey A.; Laskin, Alexander

    2015-12-15

    Atmospheric brown carbon (BrC) is an important contributor to light absorption and climate forcing by aerosols. Reactions between small water-soluble carbonyls and ammonia or amines have been identified as one of the potential pathways of BrC formation. However, detailed chemical characterization of BrC chromophores has been challenging and their formation mechanisms are still poorly understood. Understanding BrC formation is impeded by the lack of suitable methods which can unravel the variability and complexity of BrC mixtures. This study applies high performance liquid chromatography (HPLC) coupled to photodiode array (PDA) detector and high resolution mass spectrometry (HRMS) to investigate optical properties and chemical composition of individual BrC components produced through reactions of methylglyoxal (MG) and ammonium sulfate (AS), both of which are abundant in the atmospheric environment. A direct relationship between optical properties and chemical composition of 30 major BrC chromophores was established. Nearly all of these chromophores are nitrogen-containing compounds that account for >70% of the overall light absorption by the MG+AS system in the 300-500 nm range. These results suggest that reduced-nitrogen organic compounds formed in reactions between atmospheric carbonyls and ammonia/amines are important BrC chromophores. It is also demonstrated that improved separation of BrC chromophores by HPLC will significantly advance understanding of BrC chemistry.

  7. Intermediate- and high-energy reactions of uranium with neon and carbon

    International Nuclear Information System (INIS)

    Target fragment production from the interactions of 1.0, 3.0, 4.8, and 12 GeV 12C and 5.0, 8.0, 20, and 42 GeV 20Ne with uranium has been measured using off-line gamma-ray spectroscopic techniques. The experimental charge and mass yield distributions are generally consistent with the concepts of limiting fragmentation and factorization at energies of 3.0 GeV and above. The total projectile kinetic energy was found to be the relevant scaling parameter for the comparison of reactions induced by projectiles of different sizes. Light fragments with mass number less than 60 were found to violate limiting fragmentation, and had excitation functions that were strongly increasing with projectile energy until 8.0 to 12.0 GeV. With the 1.0 GeV 12C beam the pattern of mass yields was quite different from that of all the other reactions, with the normal peak in the fission mass region (80 < A < 145), but with much lower yields below mass number 60 and between mass numbers 145 and 210, indicating that these fragments are formed primarily in very energetic reactions in which large excitation energies are transferred to and significant amounts of mass are removed from the target nucleus. Theoretical predictions of the intra-nuclear cascade, nuclear fireball, and nuclear firestreak models are compared with the experimental results. The intra-nuclear cascade and nuclear firestreak models are both able to predict the general shapes of the experimental distributions, with the exception of the yields for the lightest fragments

  8. Investigation of Proton-Proton Short-Range Correlations via the 12C(e,e'pp) Reaction

    OpenAIRE

    Shneor, R.; Monaghan, P.; Subedi, R.

    2007-01-01

    We investigated simultaneously the 12C(e,e'p) and 12C(e,e'pp) reactions at Q2 = 2 [GeV/c]2, x_B = 1.2, and in an (e,e'p) missing-momentum range from 300 to 600 MeV/c. At these kinematics, with a missing-momentum greater than the Fermi momentum of nucleons in a nucleus and far from the delta excitation, short-range nucleon-nucleon correlations are predicted to dominate the reaction. For(9.5 +/- 2)% of the 12C(e,e'p) events, a recoiling partner proton was observed back-to-back to the 12C(e,e'p)...

  9. Investigation of Proton-Proton Short-Range Correlations via the 12C(e,e'pp) Reaction

    International Nuclear Information System (INIS)

    We investigated simultaneously the 12C(e,e'p) and 12C(e,e'pp) reactions at Q2=2 (GeV/c)2, xB=1.2, and in an (e, e'p) missing-momentum range from 300 to 600 MeV/c. At these kinematics, with a missing momentum greater than the Fermi momentum of nucleons in a nucleus and far from the delta excitation, short-range nucleon-nucleon correlations are predicted to dominate the reaction. For (9.5±2)% of the 12C(e,e'p) events, a recoiling partner proton was observed back-to-back to the 12C(e,e'p) missing-momentum vector, an experimental signature of correlations

  10. Investigation of Proton-Proton Short-Range Correlations via the 12C(e,e'pp) Reaction

    CERN Document Server

    Shneor, R; Subedi, R; al, et

    2007-01-01

    We investigated simultaneously the 12C(e,e'p) and 12C(e,e'pp) reactions at Q2 = 2 [GeV/c]2, x_B = 1.2, and in an (e,e'p) missing-momentum range from 300 to 600 MeV/c. At these kinematics, with a missing-momentum greater than the Fermi momentum of nucleons in a nucleus and far from the delta excitation, short-range nucleon-nucleon correlations are predicted to dominate the reaction. For(9.5 +/- 2)% of the 12C(e,e'p) events, a recoiling partner proton was observed back-to-back to the 12C(e,e'p) missing momentum vector, an experimental signature of correlations.

  11. Nitrogen, carbon, and sulfur isotopic change during heterotrophic (Pseudomonas aureofaciens) and autotrophic (Thiobacillus denitrificans) denitrification reactions

    Science.gov (United States)

    Hosono, Takahiro; Alvarez, Kelly; Lin, In-Tian; Shimada, Jun

    2015-12-01

    In batch culture experiments, we examined the isotopic change of nitrogen in nitrate (δ15NNO3), carbon in dissolved inorganic carbon (δ13CDIC), and sulfur in sulfate (δ34SSO4) during heterotrophic and autotrophic denitrification of two bacterial strains (Pseudomonas aureofaciens and Thiobacillus denitrificans). Heterotrophic denitrification (HD) experiments were conducted with trisodium citrate as electron donor, and autotrophic denitrification (AD) experiments were carried out with iron disulfide (FeS2) as electron donor. For heterotrophic denitrification experiments, a complete nitrate reduction was accomplished, however bacterial denitrification with T. denitrificans is a slow process in which, after seventy days nitrate was reduced to 40% of the initial concentration by denitrification. In the HD experiment, systematic change of δ13CDIC (from - 7.7‰ to - 12.2‰) with increase of DIC was observed during denitrification (enrichment factor εN was - 4.7‰), suggesting the contribution of C of trisodium citrate (δ13C = - 12.4‰). No SO42 - and δ34SSO4 changes were observed. In the AD experiment, clear fractionation of δ13CDIC during DIC consumption (εC = - 7.8‰) and δ34SSO4 during sulfur use of FeS2-S (around 2‰), were confirmed through denitrification (εN = - 12.5‰). Different pattern in isotopic change between HD and AD obtained on laboratory-scale are useful to recognize the type of denitrification occurring in the field.

  12. Localized surface grafting reactions on carbon nanofibers induced by gamma and e-beam irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Evora, M.C., E-mail: cecilia@ieav.cta.br [Institute for Advanced Studies-IEAV/DCTA, Av. Cel Jose Alberto Albano do Amarante, 1-Putim, 12228-001 São Jose dos Campos, SP (Brazil); Araujo, J.R., E-mail: jraraujo@inmetro.gov.br [Instituto Nacional de Metrologia, Qualidade e Tecnologia, Av. Nossa Sra. das Graças, 50, 25250-020 Duque de Caxias, RJ (Brazil); Ferreira, E.H.M. [Instituto Nacional de Metrologia, Qualidade e Tecnologia, Av. Nossa Sra. das Graças, 50, 25250-020 Duque de Caxias, RJ (Brazil); Strohmeier, B.R. [Thermo Fisher Scientific, 5225 Verona Road, Madison, WI 53711 (United States); Silva, L.G.A., E-mail: lgasilva@ipen.br [Institute for Nuclear and Energy Research- IPEN, Av. Prof lineu Prestes, 2242- Cidade Universitaria, 05508-000 SP (Brazil); Achete, C.A. [Instituto Nacional de Metrologia, Qualidade e Tecnologia, Av. Nossa Sra. das Graças, 50, 25250-020 Duque de Caxias, RJ (Brazil)

    2015-04-30

    Graphical abstract: - Highlights: • Methodology for the functionalization of carbon nanofibers was investigated. • Two radiation sources were used to promote grafting reactions: gamma and electron beam. • We report the optimum inhibitor concentration to achieve the functionalization. • Surface of carbon nanofibers showed an increase of oxygen content after irradiation. • The radiation-induced graphitization did not damage the overall sp{sup 2} structure. - Abstract: Electron beam and gamma-ray irradiation have potential application to modify the carbon fiber nanostructures in order to produce useful defects in the graphitic structure and create reactive sites. In this study, the methodology to functionalize carbon nanofiber (CNF), via a radiation process and using acrylic acid as a source of oxygen functional groups, was investigated. The samples were submitted to a direct grafting radiation process with electron beam and gamma-ray source. Several parameters were changed such as: acrylic acid concentration, radiation dose and percentage of inhibitor necessary to achieve functionalization, with higher percentage of oxygen functional groups on CNF surface, and better dispersion. The better results achieved were when mixing CNF in a solution of acrylic acid with 6% of inhibitor (FeSO{sub 4}·7H{sub 2}O) and irradiated at 100 kGy. The samples were characterized by X-ray photoelectron spectroscopy and the surface composition (atomic%) showed a significant increase of oxygen content for the samples after irradiation. Also, the dispersion of the functionalized CNF in water was stable during months which may be a good indication that the functionalization process of CNF via ionizing radiation was successful.

  13. BOREAS TGB-12 Soil Carbon and Flux Data of NSA-MSA in Raster Format

    Science.gov (United States)

    Hall, Forrest G. (Editor); Knapp, David E. (Editor); Rapalee, Gloria; Davidson, Eric; Harden, Jennifer W.; Trumbore, Susan E.; Veldhuis, Hugo

    2000-01-01

    The BOREAS TGB-12 team made measurements of soil carbon inventories, carbon concentration in soil gases, and rates of soil respiration at several sites. This data set provides: (1) estimates of soil carbon stocks by horizon based on soil survey data and analyses of data from individual soil profiles; (2) estimates of soil carbon fluxes based on stocks, fire history, drain-age, and soil carbon inputs and decomposition constants based on field work using radiocarbon analyses; (3) fire history data estimating age ranges of time since last fire; and (4) a raster image and an associated soils table file from which area-weighted maps of soil carbon and fluxes and fire history may be generated. This data set was created from raster files, soil polygon data files, and detailed lab analysis of soils data that were received from Dr. Hugo Veldhuis, who did the original mapping in the field during 1994. Also used were soils data from Susan Trumbore and Jennifer Harden (BOREAS TGB-12). The binary raster file covers a 733-km 2 area within the NSA-MSA.

  14. Final Report: The Impact of Carbonate on Surface Protonation, Electron Transfer and Crystallization Reactions in Iron Oxide Nanoparticles and Colloids

    Energy Technology Data Exchange (ETDEWEB)

    Dixon, David Adams [The University of Alabama

    2013-07-02

    This project addresses key issues of importance in the geochemical behavior of iron oxides and in the geochemical cycling of carbon and iron. For Fe, we are specifically studying the influence of carbonate on electron transfer reactions, solid phase transformations, and the binding of carbonate to reactive sites on the edges of particles. The emphasis on carbonate arises because it is widely present in the natural environment, is known to bind strongly to oxide surfaces, is reactive on the time scales of interest, and has a speciation driven by acid-base reactions. The geochemical behavior of carbonate strongly influences global climate change and CO{sub 2} sequestration technologies. Our goal is to answer key questions with regards to specific site binding, electron transfer reactions, and crystallization reactions of iron oxides that impact both the geochemical cycling of iron and CO{sub 2} species. Our work is focused on the molecular level description of carbonate chemistry in solution including the prediction of isotope fractionation factors. We have also done work on critical atmospheric species.

  15. The first chiral diene-based metal-organic frameworks for highly enantioselective carbon-carbon bond formation reactions

    Energy Technology Data Exchange (ETDEWEB)

    Sawano, Takahiro; Ji, Pengfei; McIsaac, Alexandra R.; Lin, Zekai; Abney, Carter W.; Lin, Wenbin [UC

    2016-02-01

    We have designed the first chiral diene-based metal–organic framework (MOF), E₂-MOF, and postsynthetically metalated E₂-MOF with Rh(I) complexes to afford highly active and enantioselective single-site solid catalysts for C–C bond formation reactions. Treatment of E₂-MOF with [RhCl(C₂H₄)₂]₂ led to a highly enantioselective catalyst for 1,4-additions of arylboronic acids to α,β-unsaturated ketones, whereas treatment of E₂-MOF with Rh(acac)(C₂H₄)₂ afforded a highly efficient catalyst for the asymmetric 1,2-additions of arylboronic acids to aldimines. Interestingly, E₂-MOF·Rh(acac) showed higher activity and enantioselectivity than the homogeneous control catalyst, likely due to the formation of a true single-site catalyst in the MOF. E₂-MOF·Rh(acac) was also successfully recycled and reused at least seven times without loss of yield and enantioselectivity.

  16. Up-Scaling Geochemical Reaction Rates for Carbon Dioxide (CO2) in Deep Saline Aquifers

    Energy Technology Data Exchange (ETDEWEB)

    Peters, Catherine A

    2013-02-28

    Geochemical reactions in deep subsurface environments are complicated by the consolidated nature and mineralogical complexity of sedimentary rocks. Understanding the kinetics of these reactions is critical to our ability to make long-term predictions about subsurface processes such as pH buffering, alteration in rock structure, permeability changes, and formation of secondary precipitates. In this project, we used a combination of experiments and numerical simulation to bridge the gap between our knowledge of these reactions at the lab scale and rates that are meaningful for modeling reactive transport at core scales. The focus is on acid-driven mineral dissolution, which is specifically relevant in the context of CO2-water-rock interactions in geological sequestration of carbon dioxide. The project led to major findings in three areas. First, we modeled reactive transport in pore-network systems to investigate scaling effects in geochemical reaction rates. We found significant scaling effects when CO2 concentrations are high and reaction rates are fast. These findings indicate that the increased acidity associated with geological sequestration can generate conditions for which proper scaling tools are yet to be developed. Second, we used mathematical modeling to investigate the extent to which SO2, if co-injected with CO2, would acidify formation brines. We found that there exist realistic conditions in which the impact on brine acidity will be limited due to diffusion rate-limited SO2 dissolution from the CO2 phase, and the subsequent pH shift may also be limited by the lack of availability of oxidants to produce sulfuric acid. Third, for three Viking sandstones (Alberta sedimentary basin, Canada), we employed backscattered electron microscopy and energy dispersive X-ray spectroscopy to statistically characterize mineral contact with pore space. We determined that for reactive minerals in sedimentary consolidated rocks, abundance alone is not a good predictor of

  17. Interlaboratory reaction rate program. 12th progress report, November 1976-October 1979

    Energy Technology Data Exchange (ETDEWEB)

    Lippincott, E.P.; McElroy, W.N.; Preston, C.C. (comps.)

    1980-09-01

    The Interlaboratory Reaction Rate UILRR) program is establishing the capability to accurately measure neutron-induced reactions and reaction rates for reactor fuels and materials development programs. The goal for the principal fission reactions, /sup 235/U, /sup 238/U and /sup 239/Pu, is an accuracy to within +- 5% at the 95% confidence level. Accurate measurement of other fission and nonfission reactions is also required, but to a lesser accuracy, between +- 5% and 10% at the 95% confidence level. A secondary program objective is improvement in knowledge of the nuclear parameters involved in the standarization of fuels and materials dosimetry measurements of neutron flux, spectra, fluence and burnup.

  18. Cobalt diselenide nanoparticles embedded within porous carbon polyhedra as advanced electrocatalyst for oxygen reduction reaction

    Science.gov (United States)

    Wu, Renbing; Xue, Yanhong; Liu, Bo; Zhou, Kun; Wei, Jun; Chan, Siew Hwa

    2016-10-01

    Highly efficient and cost-effective electrocatalyst for the oxygen reduction reaction (ORR) is crucial for a variety of renewable energy applications. Herein, strongly coupled hybrid composites composed of cobalt diselenide (CoSe2) nanoparticles embedded within graphitic carbon polyhedra (GCP) as high-performance ORR catalyst have been rationally designed and synthesized. The catalyst is fabricated by a convenient method, which involves the simultaneous pyrolysis and selenization of preformed Co-based zeolitic imidazolate framework (ZIF-67). Benefiting from the unique structural features, the resulting CoSe2/GCP hybrid catalyst shows high stability and excellent electrocatalytic activity towards ORR (the onset and half-wave potentials are 0.935 and 0.806 V vs. RHE, respectively), which is superior to the state-of-the-art commercial Pt/C catalyst (0.912 and 0.781 V vs. RHE, respectively).

  19. Metal-Organic Framework Derived Hierarchically Porous Nitrogen-Doped Carbon Nanostructures as Novel Electrocatalyst for Oxygen Reduction Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Shaofang; Zhu, Chengzhou; Zhou, Yazhou; Yang, Guohai; Jeon, Ju Won; Lemmon, John P.; Du, Dan; Nune, Satish K.; Lin, Yuehe

    2015-10-01

    The hierarchically porous nitrogen-doped carbon materials, derived from nitrogen-containing isoreticular metal-organic framework-3 (IRMOF-3) through direct carbonization, exhibited excellent electrocatalytic activity in alkaline solution for oxygen reduction reaction (ORR). This high activity is attributed to the 10 presence of high percentage of quaternary and pyridinic nitrogen, the high surface area as well as good conductivity. When IRMOF-3 was carbonized at 950 °C (CIRMOF-3-950), it showed four-electron reduction pathway for ORR and exhibited better stability (about 78.5% current density was maintained) than platinum/carbon (Pt/C) in the current durability test. In addition, CIRMOF-3-950 presented high selectivity to cathode reactions compared to commercial Pt/C.

  20. Formation of tungsten carbide nanoparticles on graphitized carbon to facilitate the oxygen reduction reaction

    Science.gov (United States)

    Yan, Zaoxue; He, Guoqiang; Cai, Mei; Meng, Hui; Shen, Pei Kang

    2013-11-01

    Tungsten carbide nanoparticles with the average size less than 5 nm uniformly dispersed on the graphitized carbon matrix have been successfully synthesized by a one-step ion-exchange method. This route is to locally anchor the interested species based on an ionic level exchange process using ion-exchange resin. The advantage of this method is the size control of targeted nanomaterial as well as the graphitization of resin at low temperatures catalyzed by iron salt. The Pt nanoparticles coupled with tungsten carbide nanoparticles on graphitized carbon nanoarchitecture form a stable electrocatalyst (Pt/WC-GC). The typical Pt/WC-GC electrocatalyst gives a Pt-mass activity of 247.7 mA mgPt-1, which is much higher than that of commercial Pt/C electrocatalyst (107.1 mA mgPt-1) for oxygen reduction reaction due to the synergistic effect between Pt and WC. The presented method is simple and could be readily scaled up for mass production of the nanomaterials.

  1. Effect of Co in the efficiency of the methanol electrooxidation reaction on carbon supported Pt

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez-Fernandez, P.; Montiel, M.; Ocon, P. [Dpto. Quimica-Fisica Aplicada, Facultad de Ciencias, Universidad Autonoma de Madrid (UAM), C/Francisco Tomas y Valiente 7, 28049 Madrid (Spain); Fierro, J.L.G.; Rojas, S. [Grupo de Energia y Quimica Sostenibles, Instituto de Catalisis y Petroleoquimica (CSIC), C/ Marie Curie 2, 28049 Madrid (Spain); Wang, H.; Abruna, H.D. [Department of Chemistry and Chemical Biology, Cornell University. Ithaca, NY 14853 (United States)

    2010-12-15

    The effect of Co addition to carbon nanotubes supported Pt in the methanol oxidation reaction has been investigated by means of differential electrochemical mass spectrometry (DEMS). It has been observed that the CO{sub 2} efficiency increases in carbon nanotubes supported PtCo compared to its homologous Pt catalysts, especially at potentials lower than 0.55 V. Despite of this, the Faradaic current reached by the bimetallic catalysts in the methanol electrooxidation was lower than those recorded on the monometallic samples. This is because Co addition difficult finding enough Pt vicinal sites for methanol dehydrogenation. On the other hand, it has been found that alloying Pt with Co, shifts down the d-band center of the larger element, so the strength of the interaction with adsorbates decreases. Consequently, it will be easier to oxidize CO{sub ad} on the bimetallic surface. Furthermore, the necessary -OH{sub ad} species for the CO{sub ad} oxidation to CO{sub 2} will be provided by the CNTs themselves. (author)

  2. One-pot synthesis of S-alkyl dithiocarbamates via the reaction of N-tosylhydrazones, carbon disulfide and amines.

    Science.gov (United States)

    Sha, Qiang; Wei, Yun-Yang

    2013-09-14

    A new, convenient and efficient transition metal-free synthesis of S-alkyl dithiocarbamates through one-pot reaction of N-tosylhydrazones, carbon disulfide and amines is reported. Tosylhydrazones derived from various aromatic and aliphatic ketones or aldehydes were tested and gave dithiocarbamates in good to excellent yields. The tosylhydrazones can be generated in situ without isolation, which provides a simpler one-pot method to synthesize dithiocarbamates via the reaction of carbonyl compounds, carbon disulfide and amines in the presence of 4-methylbenzenesulfonohydrazide. PMID:23863979

  3. Method for increasing -SiC yield on solid state reaction of coal fly ash and activated carbon powder

    Indian Academy of Sciences (India)

    Sulardjaka; Jamasri; M W Wildan; Kusnanto

    2011-07-01

    A novel process for increasing -SiC yield on solid state reaction of coal fly ash and micro powder activated carbon powder has been proposed. -SiC powder was synthesized at temperature 1300°C for 2 h under vacuum condition with 1 l/min argon flow. Cycling synthesis process has been developed for increasing -SiC yield on solid state reaction of coal fly ash and activated carbon powder. Synthesized products were analyzed by XRD with Cu-K radiation, FTIR spectrometer and SEM fitted with EDAX. The results show that the amount of relative -SiC is increased with the number of cycling synthesis.

  4. Bio-mass derived mesoporous carbon as superior electrode in all vanadium redox flow battery with multicouple reactions

    Science.gov (United States)

    Ulaganathan, Mani; Jain, Akshay; Aravindan, Vanchiappan; Jayaraman, Sundaramurthy; Ling, Wong Chui; Lim, Tuti Mariana; Srinivasan, Madapusi P.; Yan, Qingyu; Madhavi, Srinivasan

    2015-01-01

    We first report the multi-couple reaction in all vanadium redox flow batteries (VRFB) while using bio-mass (coconut shell) derived mesoporous carbon as electrode. The presence of V3+/V4+ redox couple certainly supplies the additional electrons for the electrochemical reaction and subsequently provides improved electrochemical performance of VRFB system. The efficient electro-catalytic activity of such coconut shell derived high surface area mesoporous carbon is believed for the improved cell performance. Extensive power and electrochemical studies are performed for VRFB application point of view and described in detail.

  5. Heteropoly Acid/Nitrogen Functionalized Onion-like Carbon Hybrid Catalyst for Ester Hydrolysis Reactions.

    Science.gov (United States)

    Liu, Wei; Qi, Wei; Guo, Xiaoling; Su, Dangsheng

    2016-02-18

    A novel heteropoly acid (HPA)/nitrogen functionalized onion-like carbon (NOLC) hybrid catalyst was synthesized through supramolecular (electrostatic and hydrogen bond) interactions between the two components. The chemical structure and acid strength of the HPA/NOLC hybrid have been fully characterized by thermogravimetric analysis, IR spectroscopy, X-ray photoelectron spectroscopy, NH3 temperature-programmed desorption and acid-base titration measurements. The proposed method for the fabrication of the HPA/NOLC hybrid catalyst is a universal strategy for different types of HPAs to meet various requirements of acidic or redox catalysis. The hydrophobic environment of NOLC effectively prevents the deactivation of HPA in an aqueous system, and the combination of uniformly dispersed HPA clusters and the synergistic effect between NOLC and HPA significantly promotes its activity in ester hydrolysis reactions, which is higher than that of bare PWA as homogeneous catalyst. The kinetics of the hydrolysis reactions indicate that the aggregation status of the catalyst particles has great influence on the apparent activity. PMID:26606266

  6. Removal of Cr (VI) with wheat-residue derived black carbon: Reaction mechanism and adsorption performance

    International Nuclear Information System (INIS)

    The removal of Cr (VI) from aqueous solutions using black carbon (BC) isolated from the burning residues of wheat straw was investigated as a function of pH, contact time, reaction temperature, supporting electrolyte concentration and analytical initial Cr (VI) concentration in batch studies. The effect of surface properties on the adsorption behavior of Cr (VI) was investigated with scanning electron microscope (SEM) equipped with the energy dispersive X-ray spectroscope (EDS) and Fourier transform-infrared (FTIR) spectroscopy. The removal mechanism of Cr (VI) onto the BC was investigated and the result showed that the adsorption reaction consumed a large amount of protons along the reduction of Cr (VI) to Cr (III). The oxidation of the BC took place concurrently to the chromium reduction and led to the formation of hydroxyl and carboxyl functions. An initial solution pH of 1.0 was most favorable for Cr (VI) removal. The adsorption process followed the pseudo-second order equation and Freundlich isotherm very well. The Cr (VI) adsorption was temperature-dependent and almost independent on the sodium chloride concentrations. The maximum adsorption capacity for Cr (VI) was found at 21.34 mg/g in an acidic medium, which is comparable to other low-cost adsorbents.

  7. A kinetic study of the electron-transfer in the reaction of tribenzylchlorotin with [COW12O40]5-

    Institute of Scientific and Technical Information of China (English)

    Fatemeh F. Bamoharram; Mohammad M. Heravi; Touran Ardalan; Pouran Ardalan

    2009-01-01

    A kinetic study of the electron-transfer in the reaction of tribenzylchlorotin with potassium 12-tungsto cobalt (Ⅲ) ate ion, K5[CoW12O40], abbreviated as Co(Ⅲ)W, has been performed in different solvents. The studies were carried out in methanol, ethanol, acetonitrile and acetic acid/water. The rate constants, reaction rates and activation parameters were calculated. Our findings show that the rate of disappearance of the Co(Ⅲ) is pseudo-first order. The kinetic data is strongly affected by used solvents. The maximum and minimum rate constants were achieved in the ethanol and acetic acid/water (70/30) as a solvent, respectively. In all of the used solvents, negative value of activation entropies was observed, but negative activation enthalpies are observed in methanol, ethanol and acetonitrile. The reaction rate is increased with increase of Co(Ⅲ) concentration.

  8. Vitamin B12: one carbon metabolism, fetal growth and programming for chronic disease.

    Science.gov (United States)

    Rush, E C; Katre, P; Yajnik, C S

    2014-01-01

    This review brings together human and animal studies and reviews that examine the possible role of maternal vitamin B12 (B12) on fetal growth and its programming for susceptibility to chronic disease. A selective literature review was undertaken to identify studies and reviews that investigate these issues, particularly in the context of a vegetarian diet that may be low in B12 and protein and high in carbohydrate. Evidence is accumulating that maternal B12 status influences fetal growth and development. Low maternal vitamin B12 status and protein intake are associated with increased risk of neural tube defect, low lean mass and excess adiposity, increased insulin resistance, impaired neurodevelopment and altered risk of cancer in the offspring. Vitamin B12 is a key nutrient associated with one carbon metabolic pathways related to substrate metabolism, synthesis and stability of nucleic acids and methylation of DNA which regulates gene expression. Understanding of factors regulating maternal-fetal one carbon metabolism and its role in fetal programming of non communicable diseases could help design effective interventions, starting with maternal nutrition before conception. PMID:24219896

  9. A kinetic study of the reaction of water vapor and carbon dioxide on uranium; Cinetique de la reaction de la vapeur d'eau et du dioxyde de carbone sur l'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Santon, J.P. [Commissariat a l' Energie Atomique, Grenoble (France). Centre d' Etudes Nucleaires

    1964-09-15

    The kinetic study of the reaction of water vapour and carbon dioxide with uranium has been performed by thermogravimetric methods at temperatures between 160 and 410 deg G in the first case, 350 and 1050 deg C in the second: Three sorts of uranium specimens were used: uranium powder, thin evaporated films, and small spheres obtained from a plasma furnace. The experimental results led in the case of water vapour, to a linear rate of reaction controlled by diffusion at the lower temperatures, and by a surface reaction at the upper ones. In the case of carbon dioxide, a parabolic law has been found, controlled by diffusional processes. (author) [French] L'etude cinetique de la reaction de la vapeur d'eau et du dioxyde de carbone sur l'uranium a ete entreprise au moyen de methodes thermogravimetriques, dans te premier cas entre 160 et 410 deg C et dans le second entre 350 et 1050 deg C. Le materiau utilise se presentait sous trois formes: poudres, couches minces evaporees et billes obtenues par fusion en chalumeau a plasma. Les resultats experimentaux ont permis de mettre en evidence, dans le cas de la vapeur d'eau, une cinetique lineaire controlee par la diffusion a basse temperature et d'interface a haute temperature. Dans le cas du dioxyde de carbone par contre, on trouve une cinetique parabolique controlee par la diffusion. (auteur)

  10. Carbonation of lignite fly ash at ambient T and P in a semi-dry reaction system for CO{sub 2} sequestration

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, Markus, E-mail: markus.bauer1@uni-bayreuth.de [Department of Hydrology, University of Bayreuth, D-95440 Bayreuth (Germany); Gassen, Niklas [Department of Hydrology, University of Bayreuth, D-95440 Bayreuth (Germany); Stanjek, Helge [Clay and Interface Mineralogy, RWTH Aachen University, D-52072 Aachen (Germany); Peiffer, Stefan [Department of Hydrology, University of Bayreuth, D-95440 Bayreuth (Germany)

    2011-08-15

    Highlights: > The carbonation of lignite fly ash was achieved under semi dry conditions at low temperature and pressure conditions. > Highest CO{sub 2}-uptake was reached for intermediate liquid-to-solid ratios of 0.12-0.18 L kg{sup -1}. > Increasing mixing intensity or pCO{sub 2} caused higher carbonation rates, suggesting limitation by CO{sub 2} supply. > Up to 4.8 mmol CO{sub 2} g{sup -1} were absorbed, corresponding to 53% of the theoretical CO{sub 2} binding capacity of the material. > Both Ca and Mg containing phases were converted into carbonate minerals. - Abstract: The global rise in atmospheric greenhouse gas concentrations calls for practicable solutions to capture CO{sub 2}. In this study, a mineral carbonation process was applied in which CO{sub 2} reacts with alkaline lignite ash and forms stable carbonate solids. In comparison to previous studies, the assays were conducted at low temperatures and pressures and under semi-dry reaction conditions in an 8 L laboratory mixing device. In order to find optimum process conditions the pCO{sub 2} (10-20%), stirring rate (500-3000 rpm) and the liquid to solid ratio (L/S = 0.03-0.36 L kg{sup -1}) were varied. In all experiments a considerable CO{sub 2} uptake from the gas phase was observed. Concurrently the solid phase contents of Ca and Mg (hydr)oxides decreased and CaCO{sub 3} and MgCO{sub 3} fractions increased throughout the experiments, showing that CO{sub 2} was stabilized as a solid carbonate. The carbonation reaction depends on three factors: Dissolution of CO{sub 2} in the liquid phase, mobilization of Ca and Mg from the mineral surface and precipitation of the carbonate solids. Those limitations were found to depend strongly on the variation of the process parameters. Optimum reaction conditions could be found for L/S ratios between 0.12 and 0.18, medium stirring velocities and pCO{sub 2} between 10% and 20%. Maximum CO{sub 2} uptake by the solid phase was 4.8 mmol g{sup -1} after 120 min

  11. Reproducibly creating hierarchical 3D carbon to study the effect of Si surface functionalization on the oxygen reduction reaction

    Science.gov (United States)

    Zeng, Yuze; Flores, Jose F.; Shao, Yu-Cheng; Guo, Jinghua; Chuang, Yi-De; Lu, Jennifer Q.

    2016-06-01

    We report a new method to reproducibly fabricate functional 3D carbon structures directly on a current collector, e.g. stainless steel. The 3D carbon platform is formed by direct growth of upright arrays of carbon nanofiber bundles on a roughened surface of stainless steel via the seed-assisted approach. Each bundle consists of about 30 individual carbon nanofibers with a diameter of 18 nm on average. We have found that this new platform offers adequate structural integrity. As a result, no reduction of the surface area during downstream chemical functionalization was observed. With a fixed and reproducible 3D structure, the effect of the chemistry of the grafted species on the oxygen reduction reaction has been systematically investigated. This investigation reveals for the first time that non-conductive Si with an appropriate electronic structure distorts the carbon electronic structure and consequently enhances ORR electrocatalysis. The strong interface provides excellent electron connectivity according to electrochemical analysis. This highly reproducible and stable 3D platform can serve as a stepping-stone for the investigation of the effect of carbon surface functionalization on electrochemical reactions in general.We report a new method to reproducibly fabricate functional 3D carbon structures directly on a current collector, e.g. stainless steel. The 3D carbon platform is formed by direct growth of upright arrays of carbon nanofiber bundles on a roughened surface of stainless steel via the seed-assisted approach. Each bundle consists of about 30 individual carbon nanofibers with a diameter of 18 nm on average. We have found that this new platform offers adequate structural integrity. As a result, no reduction of the surface area during downstream chemical functionalization was observed. With a fixed and reproducible 3D structure, the effect of the chemistry of the grafted species on the oxygen reduction reaction has been systematically investigated. This

  12. Analysis of Neutron Double-Differential Cross Sections for n + 12C Reaction Below 30 MeV

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Based on the light nucleus reaction model (Nucl. Sci. Eng. l33 (1999) 218), four aspects (neutron incident energy region, reaction channel analysis, the renewed level schemes and the optical model parameters) of n+12 C reaction are improved to calculate total outgoing neutron double-differential cross sections with modified LUNF code below 30 MeV. The calculated results agree fairly well with the experimental data at En = 14.1 MeV and 18 MeV. The analysis shows that the pre-equilibrium mechanism, which is exactly considered the conservation of energy, momentum and parity, dominates the whole reaction process. The contribution of the neutron emission from 5He to total energyangular spectra is also considered properly. This modified LUNF code will be a useful tool to set up the file of neutron double-differential cross sections below 30 MeV in the neutron evaluation nuclear data library.

  13. The kinetics of the O2/CO2 reaction in molten carbonate - Reaction orders for O2 and CO2 on NiO. [in fuel cells

    Science.gov (United States)

    Winnick, J.; Ross, P. N.

    1980-01-01

    The kinetics of the O2/CO2 reaction in molten carbonate is investigated using paste electrolytes and nickel sinter electrodes. A two-step approach to the determination of reaction orders is employed. First, exchange currents at various P(CO2) and P(O2) were measured using the low polarization method. Second, alpha(+) and alpha(-) values were obtained from the slope of the Allen-Hickling plot for current densities low enough so that concentration polarization within the electrode can be neglected. The reaction orders are + 1/4 in CO2 and + 5/8 in O2 in the cathodic direction, and - 3/4 in CO2 and + 1/8 in O2 in the anodic direction.

  14. Original Reaction Sequence of Pb(Yb1/2Nb1/2)O3-PbTiO3: Consequences on Dielectric Properties and Chemical Order

    OpenAIRE

    Charlotte Cochard; Fabienne Karolak; Christine Bogicevic; Orland Guedes; Pierre-Eymeric Janolin

    2015-01-01

    The solid solution [Pb(Yb1/2Nb1/2)O3]1−x-[PbTiO3]x was synthesized with x≤60%, using several high-temperature techniques as well as room-temperature mechanosynthesis. The high-temperature synthesis reveals a reaction path involving the synthesis first of the end-members before the solid solution. The density and dielectric constant measured on the ceramics prepared from these powders indicate the crucial role of the synthesis technique in the subsequent properties. Mechanosynthesis results in...

  15. Crossed-beam reaction of carbon atoms with hydrocarbon molecules. IV. Chemical dynamics of methylpropargyl radical formation, C{sub 4}H{sub 5}, from reaction of C({sup 3}P{sub j}) with propylene, C{sub 3}H{sub 6} (X{sup 1}A)

    Energy Technology Data Exchange (ETDEWEB)

    Kaiser, R.I.; Stranges, D.; Bevsek, H.M.; Lee, Y.T.; Suits, A.G. [Department of Chemistry, University of California, Berkeley, California 94720 (United States)]|[Chemical Sciences Division, Berkeley National Laboratory, Berkeley, California 94720 (United States)

    1997-03-01

    The reaction between ground state carbon atoms and propylene, C{sub 3}H{sub 6}, was studied at average collision energies of 23.3 and 45.0 kJmol{sup {minus}1} using the crossed molecular beam technique. Product angular distributions and time-of-flight spectra of C{sub 4}H{sub 5} at m/e=53 were recorded. Forward-convolution fitting of the data yields a maximum energy release as well as angular distributions consistent with the formation of methylpropargyl radicals. Reaction dynamics inferred from the experimental results suggest that the reaction proceeds on the lowest {sup 3}A surface via an initial addition of the carbon atom to the {pi}-orbital to form a triplet methylcyclopropylidene collision complex followed by ring opening to triplet 1,2-butadiene. Within 0.3{endash}0.6 ps, 1,2-butadiene decomposes through carbon{endash}hydrogen bond rupture to atomic hydrogen and methylpropargyl radicals. The explicit identification of C{sub 4}H{sub 5} under single collision conditions represents a further example of a carbon{endash}hydrogen exchange in reactions of ground state carbon with unsaturated hydrocarbons. This versatile machine represents an alternative pathway to build up unsaturated hydrocarbon chains in combustion processes, chemical vapor deposition, and in the interstellar medium. {copyright} {ital 1997 American Institute of Physics.}

  16. Study of the p+{sup 12}C reaction at energies up to 30 MeV

    Energy Technology Data Exchange (ETDEWEB)

    Harada, Masahide; Yamamoto, A.; Yoshioka, S. [Kyushu Univ., Fukuoka (Japan)] [and others

    1998-03-01

    Double differential cross sections of charged-particles emitted in the p+{sup 12}C reaction were measured in the energy region from 14 to 26 MeV. The observed continuous components of emitted protons and {alpha}-particles were analyzed by assuming sequential decay of intermediate reaction products and/or simultaneous breakup process. It was found that the three body simultaneous decay, p+{alpha}+{sup 8}Be, and the sequential decay via p+{sup 12}C{sup *}{sub 3-} and {alpha}+{sup 9}B{sub g.s.} are most important in the proton-induced breakup of {sup 12}C for energies up to 30 MeV. (author)

  17. Nickel-catalyzed cross-coupling reactions of o-carboranyl with aryl iodides: facile synthesis of 1-aryl-o-carboranes and 1,2-diaryl-o-carboranes.

    Science.gov (United States)

    Tang, Cen; Xie, Zuowei

    2015-06-22

    A nickel-catalyzed arylation at the carbon center of o-carborane cages has been developed, thus leading to the preparation of a series of 1-aryl-o-carboranes and 1,2-diaryl-o-carboranes in high yields upon isolation. This method represents the first example of transition metal catalyzed C,C'-diarylation by cross-coupling reactions of o-carboranyl with aryl iodides. PMID:25959849

  18. Platinum Nanoparticles Supported on Nitrobenzene-Functionalized Multiwalled Carbon Nanotube as Efficient Electrocatalysts for Methanol Oxidation Reaction

    International Nuclear Information System (INIS)

    Graphical abstract: Multiwalled carbon nanotube was functionalized with nitrobenzene as a promising support material for Pt-based electrocatalysts (Pt-NB-MWCNT) for methanol oxidation. The as-prepared catalysts have higher electrocatalytic activity in terms of both mass and specific activities, and improved durability for methanol oxidation reaction than as compared to the undoped materials. - Highlights: • Multiwalled carbon nanotube was functionalized with nitrobenzene as a support material for Pt-based electrocatalysts for methanol oxidation. • The electronic properties of carbon nanotubes were modified by the nitrobenzene functionalization. • Nitrobenzene-functionalized electrocatalysts revealing the improved electrocatalytic performance of Pt-NB-MWCNT catalyst for the methanol oxidation reaction. - Abstract: A novel method of molecular covalently functionalized multiwalled carbon nanotube using nitrobenzene group is prepared and used as a promising support material of Pt-based electrocatalysts (denoted as Pt-NB-MWCNT) for methanol oxidation reaction. The physical and chemical characteristics are performed by X-ray powder diffraction, transmission electron microscopy, Raman spectroscopy, thermogravimetric and X-ray photoelectron spectroscopy. The electrocatalytic are evaluated by cyclic voltammetry and chronoamperometry techniques. Compared with the un-functionalized Pt-MWCNT catalyst, Pt-NB-MWCNTs show more uniform particle dispersion, smaller particle size, improved activity and durability for methanol oxidation reaction. The nitrobenzene group is demonstrated to promote the electrocatalytic activity of Pt-MWCNT for methanol oxidation significantly. The results represent a novel approach to functionalize MWCNT in a simple and economic way to prepare efficient electrocatalysts for methanol oxidation

  19. Microcalorimetric Adsorption of Alumina Oxide Catalysts for Combination of Ethylbenzene dehydrogenation and carbon Dioxide Shift-reaction

    Institute of Scientific and Technical Information of China (English)

    GE Xin; SHEN Jian-yi

    2004-01-01

    Styrene (STY) is now produced industrially in fairly large quantities by the dehydrogenation of ethylbenzene (EB) using promoted iron oxide catalyst with superheated steam.In this case, small amount of carbon dioxide formed as a by-product was known to inhibit the catalytic activity of commercial catalyst. Recently, there have been some reports which carbon dioxide showed positive effects to promote catalytic activities on the reaction over several catalysts.In this study, we attempted to combine the dehydrogenation of EB to STY with the carbon dioxide shift-reaction. The combine reaction (EB + CO2 → STY + H2O + CO) can be considered as one of the ways of using CO2 resources and can yield simultaneously STY and Carbon oxide.Alumina oxide catalysts such as Al2O3, Na2O/Al2O3 and K2O/Al2O3 were prepared by the usual impregnation method with an aqueous solution of NaNO3 and KNO3, and then calcined at 650℃ for 5 h in a stream of air. The reaction condition is 600℃, flow of CO2 38ml/mon and space velocity (EB) 1.28h-1.

  20. Two-neutron transfer reaction mechanisms in $^{12}$C($^6$He,$^{4}$He)$^{14}$C using a realistic three-body $^{6}$He model

    CERN Document Server

    Smalley, D; Nunes, F M; Brown, B A; Adsley, P; Al-Falou, H; Andreoiu, C; Baartman, B; Ball, G C; Blackmon, J C; Boston, H C; Catford, W N; Chagnon-Lessard, S; Chester, A; Churchman, R M; Cross, D S; Diget, C Aa; Di Valentino, D; Fox, S P; Fulton, B R; Garnsworthy, A; Hackman, G; Hager, U; Kshetri, R; Orce, J N; Orr, N A; Paul, E; Pearson, M; Rand, E T; Rees, J; Sjue, S; Svensson, C E; Tardiff, E; Varela, A Diaz; Williams, S J; Yates, S

    2014-01-01

    The reaction mechanisms of the two-neutron transfer reaction $^{12}$C($^6$He,$^4$He) have been studied at 30 MeV at the TRIUMF ISAC-II facility using the SHARC charged-particle detector array. Optical potential parameters have been extracted from the analysis of the elastic scattering angular distribution. The new potential has been applied to the study of the transfer angular distribution to the 2$^+_2$ 8.32 MeV state in $^{14}$C, using a realistic 3-body $^6$He model and advanced shell model calculations for the carbon structure, allowing to calculate the relative contributions of the simultaneous and sequential two-neutron transfer. The reaction model provides a good description of the 30 MeV data set and shows that the simultaneous process is the dominant transfer mechanism. Sensitivity tests of optical potential parameters show that the final results can be considerably affected by the choice of optical potentials. A reanalysis of data measured previously at 18 MeV however, is not as well described by th...

  1. Crystalline and tensile properties of carbon nanotube and graphene reinforced polyamide 12 fibers

    Science.gov (United States)

    Chatterjee, S.; Nüesch, F. A.; Chu, B. T. T.

    2013-02-01

    The influence of carbon nanotubes (CNTs) and graphene nanoplatelets (GnPs) on the structure and mechanical properties of polyamide 12 (PA12) fibers was investigated. As seen from wide-angle X-ray diffraction analysis the crystallinity index increases with incorporation of nanofillers due to nucleation effects. Marked improvement was noted for mechanical properties of the composites with increase in elastic modulus, yield stress and strength of the fibers. The most significant improvement of a factor of 4 could be observed for elastic modulus with the inclusion of 0.5 wt.% GnP. A comparative study was made between the fibers reinforced with CNTs and GnPs.

  2. Fragment emission in reactions of 18.5-GeV 12C ions with complex nuclei

    International Nuclear Information System (INIS)

    The emission of fragments ranging from 24Na to 52Mn in reactions of 18.5 GeV 12C ions with Cu, Ag, Gd, Ta, Au, and U targets has been studied by means of activation techniques. The experiments involved determination of the fragment production cross sections and thick-target recoil properties. The latter were used to obtain mean fragment kinetic energies and values of β/sub parallel to/, the forward velocity component of the struck nucleus (in units of c). The results are compared with similar data for incident protons of the same total kinetic energy. The data may be used to assess the importance of central collisions in fragment production. Such collisions lead to the near total destruction of both interacting nuclei and the resulting fragments are emitted by a system of intermediate rapidity. In such a process, the factorization hypothesis, which has been shown to be valid for target and projectile fragmentation reactions, should not be obeyed. A test for factorization is performed by means of a relation which states that the ratio of the cross sections for producing fragment /sup A/Z in 12C reactions to that for producing the same fragment in proton reactions with the same target is unity, provided both cross sections are reduced by the values of the corresponding total reaction cross sections sigma/sub R/, and evaluated for the same total kinetic energy of the projectile. The results of this comparison for the targets studied are presented and discussed

  3. Radial deformation of single-walled carbon nanotubes on quartz substrates and the resultant anomalous diameter-dependent reaction selectivity

    Institute of Scientific and Technical Information of China (English)

    Juan Yang; Yu Liu; Daqi Zhang; Xiao Wang; Ruoming Li; Yan Li

    2015-01-01

    Owing to the unique conjugated structure, the chemical-reaction selectivity of single-walled carbon nanotubes (SWNTs) has attracted great attention. By utilizing the radial deformation of SWNTs caused by the strong interactions with the quartz lattice, we achieve an anomalous diameter-dependent reaction selectivity of quartz lattice-oriented SWNTs in treatment with iodine vapor; this is distinctly different from the widely reported and well accepted higher reaction activity in small-diameter tubes compared to large-diameter tubes. The radial deformation of SWNTs on quartz substrate is verified by detailed Raman spectroscopy and mappings in both G-band and radial breathing mode. Due to the strong interaction between SWNTs and the quartz lattice, large-diameter tubes present a larger degree of radial deformation and more delocalized partial electrons are distributed at certain sidewall sites with high local curvature. It is thus easier for the carbon--carbon bonds at these high-curvature sites on large-diameter tubes to break down during reaction. This anomalous reaction activity offers a novel approach for selective removal of small-band~aD large-diameter tubes.

  4. Studies on 12 V substrate-integrated lead-carbon hybrid ultracapacitors

    Indian Academy of Sciences (India)

    A Banerjee; A K Shukla

    2015-05-01

    A cost-effective 12 V substrate-integrated lead-carbon hybrid ultracapacitor is developed and performance tested. These hybrid ultracapacitors employ flexible-graphite sheets as negative plate currentcollectors that are coated amperometrically with a thin layer of conducting polymer, namely poly-aniline to provide good adhesivity to activated-carbon layer. The positive plate of the hybrid ultracapacitors comprise conventional lead-sheet that is converted electrochemically into a substrate-integrated lead-dioxide electrode. 12 V substrate-integrated lead-carbon hybrid ultracapacitors both in absorbent-glass-mat and polymeric silicagel electrolyte configurations are fabricated and characterized. It is possible to realize 12 V configurations with capacitance values of ∼200 F and ∼300 F, energy densities of ∼1.9 Wh kg−1 and ∼2.5 Wh kg−1 and power densities of ∼2 kW kg−1 and ∼0.8 kW kg−1, respectively, having faradaic-efficiency values of ∼90 % with cycle-life in excess of 100,000 cycles. The effective cost of the mentioned hybrid ultracapacitors is estimated to be about ∼4 US$/Wh as compared to ∼20 US$/Wh for commercially available ultracapacitors.

  5. Simulation Experiments on the Reaction of CH4-CaSO4 and Its Carbon Kinetic Isotope Fractionation

    Institute of Scientific and Technical Information of China (English)

    YueChangtao; LiShuyuan; DingKangle; ZhongNingning

    2005-01-01

    Thermochemical sulfate reduction (TSR) in geological deposits can account for the accumulation of H,S in deep sour gas reservoirs. In this paper, thermal simulation experiments on the reaction of CH4-CaSO4 were carried out using an autoclave at high temperatures and high pressures. The products were characterized with analytical methods including carbon isotope analysis. It is found that the reaction can proceed to produce H2S, H2O and CaCO3 as the main products. Based on the experimental results, the carbon kinetic isotope fractionation was investigated, and the value of Ki(kinetic isotope effect) was calculated. The results obtained in this paper can provide useful information to explain the occurrence of H2S in deep carbonate gas reservoirs.

  6. Amorphous Molybdenum Sulfide on Graphene-Carbon Nanotube Hybrids as Highly Active Hydrogen Evolution Reaction Catalysts.

    Science.gov (United States)

    Pham, Kien-Cuong; Chang, Yung-Huang; McPhail, David S; Mattevi, Cecilia; Wee, Andrew T S; Chua, Daniel H C

    2016-03-01

    In this study, we report on the deposition of amorphous molybdenum sulfide (MoSx, with x ≈ 3) on a high specific surface area conductive support of Graphene-Carbon Nanotube hybrids (GCNT) as the Hydrogen Evolution Reaction (HER) catalysts. We found that the high surface area GCNT electrode could support the deposition of MoSx at much higher loadings compared with simple porous carbon paper or flat graphite paper. The morphological study showed that MoSx was successfully deposited on and was in good contact with the GCNT support. Other physical characterization techniques suggested the amorphous nature of the deposited MoSx. With a typical catalyst loading of 3 mg cm(-2), an overpotential of 141 mV was required to obtain a current density of 10 mA cm(-2). A Tafel slope of 41 mV decade(-1) was demonstrated. Both measures placed the MoSx-deposited GCNT electrode among the best performing molybdenum sulfide-based HER catalysts reported to date. The electrode showed a good stability with only a 25 mV increase in overpotential required for a current density of 10 mA cm(-2), after undergoing 500 potential sweeps with vigorous bubbling present. The current density obtained at -0.5 V vs SHE (Standard Hydrogen Electrode potential) decreased less than 10% after the stability test. The deposition of MoSx on high specific surface area conductive electrodes demonstrated to be an efficient method to maximize the catalytic performance toward HER. PMID:26864503

  7. {sup 16}O resonances near 4α threshold through {sup 12}C({sup 6}Li,d) reaction

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, M. R. D.; Borello-Lewin, T.; Miyake, H.; Horodynski-Matsushigue, L. B.; Duarte, J. L. M.; Rodrigues, C. L.; Faria, P. Neto de [Instituto de Física, Universidade de São Paulo, Caixa Postal 66318, CEP 05314-970, São Paulo, SP (Brazil); Cunsolo, A.; Cappuzzello, F.; Foti, A.; Agodi, C.; Cavallaro, M. [INFN - Laboratori Nazionali del Sud, Via S. Sofia 62, 95125 Catania (Italy); Napoli, M. di; Ukita, G. M. [Faculdade de Psicologia, Universidade de Santo Amaro, R. Prof. Eneas da Siqueira Neto, 340, CEP 04829-300, São Paulo, SP (Brazil)

    2014-11-11

    Several narrow alpha resonant {sup 16}O states were detected through the {sup 12}C({sup 6}Li,d) reaction, in the range of 13.5 to 17.5 MeV of excitation energy. The reaction was measured at a bombarding energy of 25.5 MeV employing the São Paulo Pelletron-Enge-Spectrograph facility and the nuclear emulsion technique. Experimental angular distributions associated with natural parity quasi-bound states around the 4α threshold are presented and compared to DWBA predictions. The upper limit for the resonance widths obtained is near the energy resolution (15 keV)

  8. Role of reaction resistance in limiting carbon monoxide uptake in rabbit lungs.

    Science.gov (United States)

    Heller, H; Schuster, K

    1998-06-01

    The contribution of reaction resistance to overall resistance to pulmonary carbon monoxide (CO) uptake [DLCO/(ThetaCO . Vc), where DLCO is lung CO diffusing capacity, ThetaCO is CO uptake conductance of erythrocytes, and Vc is pulmonary capillary blood volume] was determined in 10 anesthetized, paralyzed, and artificially ventilated rabbits. On the basis of the classical double-reciprocal equation of F. G. W. Roughton and R. E. Forster (J. Appl. Physiol. 11: 290-302, 1957), DLCO/(ThetaCO . Vc) was obtained by solving the relation DLCO/(ThetaCO . Vc) = 1 - 2/(DLNO/DLCO), where DLNO/DLCO represents the ratio between the respective single-breath diffusing capacities (DL) of nitric oxide (NO) and CO pulmonary capillary blood. The lungs of eight rabbits were inflated, starting from residual volume, by using 55 ml of indicator gas mixture (0.2% CO and 0.05% NO in nitrogen). DL values were calculated by taking the end-tidal partial pressures of CO and NO as analyzed by using a respiratory mass spectrometer. The overall value was DLCO/(ThetaCO . Vc) = 0.4 +/- 0.025 (mean +/- SD). Because of the use of O2-free indicator gas mixtures, the end-tidal O2 partial pressures were approximately 21 Torr. In one other rabbit, the application of 0.2% CO and 0.001% NO yielded DLCO/(ThetaCO . Vc) = 0.39; in the tenth rabbit, however, inspiratory volume was varied, and an identical value was found at functional residual capacity. We conclude that the contribution of reaction resistance to overall resistance to pulmonary CO uptake is independent of the inspiratory NO concentration used, including, with respect to the pertinent literature, the conclusion that in rabbits, dogs, and humans this contribution amounts to 40% when determined at functional residual capacity.

  9. Experimental Study on Hydrocarbon Formation Due to Reactions Between Carbonates and Water or Water—Bearing Minerals in Deep Earth

    Institute of Scientific and Technical Information of China (English)

    翁克难; 汪本善; 等

    1999-01-01

    In order to investigate the mechanism of formation of abiogenetic hydrocarbons at the depth of the Earth,experimental research on reactions between carbonates and water or waterbearing minerals was carried out at the pressure of about 1GPa and the temperature range of 800-1500℃.The reactions took place in an open and nonequilibrium state.Chromatographic analyses of the gas products indicate that in the experiments there were generated CH4-dominated hydrocarbons,along with some CO2 and CO.Accordingly,we think there is no essential distinction between free-state water and hydroxy in the minerals in the process of hydrocarbon formation.This study indicates that reactions between carbonates and water or water-bearing minerals should be an important factor leading to the formation of abiogenetic hydrocarbons at the Earth's depth.

  10. Highly vibrationally excited CO generated in a low-temperature chemical reaction between carbon vapor and molecular oxygen

    Science.gov (United States)

    Jans, E.; Frederickson, K.; Yurkovich, M.; Musci, B.; Rich, J. W.; Adamovich, I. V.

    2016-08-01

    A chemical flow reactor is used to study the vibrational population distribution of CO produced by a reaction between carbon vapor generated in an arc discharge and molecular oxygen. The results demonstrate formation of highly vibrationally excited CO, up to vibrational level v = 14, at low temperatures, T = 400-450 K, with population inversion at v = 4-7, in a collision-dominated environment, 15-20 Torr. The average vibrational energy per CO molecule formed by the reaction is 0.6-1.2 eV/molecule, which corresponds to 10-20% of reaction enthalpy. The results show feasibility of development of a new CO chemical laser using carbon vapor and oxygen as reactants.

  11. Thick-target neutron, gamma-ray, and radionuclide production for protons below 12 MeV on nickel and carbon beam-stops

    Energy Technology Data Exchange (ETDEWEB)

    Chadwick, M.B.; Young, P.G.; Wilson, W.B.

    1998-03-01

    Nuclear model calculations using the GNASH code are described for protons below 12 MeV incident on nickel and carbon isotopes, for beam stop design in the Los Alamos Accelerator Production of Tritium Low Energy Demonstration Accelerator (LEDA) project. The GNASH calculations apply Hauser-Feshbach and preequilibrium reaction theories and can make use of pre-calculated direct reaction cross sections to low-lying residual nucleus states. From calculated thin target cross sections, thick target 6.7 MeV and 12 MeV proton-induced production of neutrons, gamma rays, and radionuclides are determined. Emission spectra of the secondary neutrons and gamma rays are also determined. The model calculations are validated through comparisons with experimental thin- and thick-target measurements. The results of this work are being utilized as source terms in MCNP analyses for LEDA.

  12. Study of removal of Direct Yellow 12 by cadmium oxide nanowires loaded on activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Ghaedi, Mehrorang, E-mail: m_ghaedi@mail.yu.ac.ir [Chemistry Department, Yasouj University Yasouj 75914-35 (Iran, Islamic Republic of); Sadeghian, Batuol [Chemistry Department, Yasouj University Yasouj 75914-35 (Iran, Islamic Republic of); Kokhdan, Syamak Nasiri, E-mail: syamak.nasiri@yahoo.com [Chemistry Department, Yasouj University Yasouj 75914-35 (Iran, Islamic Republic of); Pebdani, Arezou Amiri [Chemistry Department, Yasouj University Yasouj 75914-35 (Iran, Islamic Republic of); Sahraei, Reza; Daneshfar, Ali; Mihandoost, Asma [Department of Chemistry, University of Ilam, P.O. Box: 65315-516, Ilam (Iran, Islamic Republic of)

    2013-05-01

    In this research, cadmium oxide nanowires loaded on activated carbon (CdO-NW-AC) has been synthesized by a simple procedure and characterized by different techniques such as XRD, SEM and UV–vis spectrometry. This new adsorbent has been efficiently utilized for the removal of the Direct Yellow 12 (DY-12) from wastewater. To obtain maximum DY-12 removal efficiency, the influences of variables such as pH, DY-12 concentration, amount of CdO-NW-AC, contact time, and temperature have been examined and optimized in a batch method. Following the variable optimization, the experimental equilibrium data (at different concentration of DY-12) was fitted to conventional isotherm models such as Langmuir, Freundlich and Tempkin. The applicability of each method is based on the R{sup 2} and error analysis for each model. It was found that the experimental equilibrium data well fitted to the Langmuir isotherm model. The dependency of removal process to time and the experimental data follow second order kinetic model with involvement of intraparticle diffusion model. The negative value of Gibbs's free energy and positive value of adsorption enthalpy show the spontaneous and endothermic nature of adsorption process. - Graphical abstract: Typical FE-SEM image of the CdO nanowires. Highlights: ► Cadmium oxide nanowires loaded on activated carbon was utilized as an adsorbent. ► It was used for the removal of Direct Yellow 12 from aqueous solutions. ► The adsorption of Direct Yellow 12 on this adsorbent is endothermic in nature. ► The adsorption equilibrium data was well described by the Langmuir isotherm model.

  13. Science Letters: Nitrogen doping of activated carbon loading Fe2O3 and activity in carbon-nitric oxide reaction

    Institute of Scientific and Technical Information of China (English)

    WAN Xian-kai; ZOU Xue-quan; SHI Hui-xiang; WANG Da-hui

    2007-01-01

    Nitrogen doping of activated carbon loading Fe2O3 was performed by annealing in ammonia, and the activity of the modified carbon for NO reduction was studied in the presence of oxygen. Results show that Fe2O3 enhances the amount of surface oxygen complexes and facilitates nitrogen incorporation in the carbon, especially in the form of pyridinic nitrogen. The modified carbon shows excellent activity for NO reduction in the low temperature regime (<500 ℃) because of the cooperative effect of Fe2O3 and the surface nitrogen species.

  14. Germanomolybdate (GeMo12O404−) Modified Carbon Nanotube Composites for Electrochemical Capacitors

    International Nuclear Information System (INIS)

    Highlights: • GeMo12O404− (GeMo) was deposited onto MWCNT to fabricate capacitive electrodes. • GeMo electrode showed excellent conductivity and 6X the capacitance of bare MWCNT. • GeMo was superimposed with PMo12O403− or SiMo12O404− on dual-layer electrodes. • Dual-layer electrodes showed combination of both molecules and 12X bare capacitance. - Abstract: Keggin type germanomolybdate, GeMo12O404− (GeMo), was deposited onto multi-walled carbon nanotubes (MWCNT) via layer-by-layer (LbL) deposition to form composite electrodes for electrochemical capacitors (ECs). The GeMo composite electrode demonstrated charge storage six times greater than that of the bare MWCNT electrode while maintaining excellent conductivity and cycling stability. GeMo also demonstrated charge storage complementary to that of the commercial Keggin type POMs, PMo12O403− (PMo) and SiMo12O404− (SiMo). Dual-layer coatings superimposing GeMo with either PMo or SiMo showed an additive combination of both active layers, which resulted in cyclic voltammograms (CVs) with overlapping redox features and charge storage twelve times greater than that of the bare MWCNT electrode. Scanning Electron Microscopy (SEM) demonstrated successful single and dual layer coating of POMs on MWCNT with high coverage and uniform surface morphologies

  15. In situ observation of the reaction of scandium and carbon by neutron diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Juarez-Arellano, Erick A., E-mail: eajuarez@unpa.edu.m [Institut fuer Geowissenschaften, Universitaet Frankfurt, Altenhoeferallee 1, 60438 Frankfurt a.M. (Germany); Universidad del Papaloapan, Circuito Central 200, Parque Industrial, Tuxtepec 68301 (Mexico); Winkler, Bjorn [Institut fuer Geowissenschaften, Universitaet Frankfurt, Altenhoeferallee 1, 60438 Frankfurt a.M. (Germany); Vogel, Sven C. [Los Alamos National Laboratory, Lujan Center. Mail Stop H805, Los Alamos, NM 87545 (United States); Senyshyn, Anatoliy [Forschungsneutronenquelle Heinz Maier-Leibnitz (FRM II), Technische Universitaet Muenchen, Lichtenbergstr. 1, D-85747 Garching (Germany); Materialwissenschaft, TU Darmstadt, Petersensstr. 23, D-64287 Darmstadt (Germany); Kammler, Daniel R. [Sandia National Laboratories, Albuquerque, NM 87185 (United States); Avalos-Borja, Miguel [CNyN, UNAM, A. Postal 2681, Ensenada, B.C. (Mexico)

    2011-01-05

    Research highlights: {yields} Exist two ScC cubic phases with B1-structure type differing in site occupancy of C. {yields} A new orthorhombic scandium carbide phase is formed at 1473(50) K. {yields} The recrystallization of alpha-Sc occurs between 1000 and 1223 K. - Abstract: The formation of scandium carbides by reaction of the elements has been investigated by in situ neutron diffraction up to 1823 K. On heating, the recrystallization of {alpha}-Sc occurs between 1000 and 1223 K. The formation of Sc{sub 2}C and ScC (NaCl-B1 type structure) phases has been detected at 1323 and 1373 K, respectively. The formation of a new orthorhombic scandium carbide phase was observed at 1473(50) K. Once the scandium carbides are formed they are stable upon heating or cooling. No other phases were detected in the present study, in which the system was always carbon saturated. The thermal expansion coefficients of all phases have been determined, they are constant throughout the temperature interval studied.

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

    Institute of Scientific and Technical Information of China (English)

    ZHOU Lei; ZHANG WeiDe; JIANG HuanFeng

    2008-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

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

  18. Observation and analysis of incomplete fusion reactions induced by (12C, 14N, 16O, 22Ne) ions

    International Nuclear Information System (INIS)

    The mechanism of the reactions induced by heavy ions has been studied. The experiments were concerned with incident channels which lead to the formation of intermediate nuclei with atomic mass (6412C, 14N, 16O, 22Ne) as projectiles respectively. The detection of light fragments (2< Z<12) is studied. A three solid-state-detector telescope, with associated electronics is used which allows the separation of reaction products according to their charge. The main features of deep inelastic collisions are discussed: large kinetic energy loss, and important nucleon transfer as a function of the angular detection. The time evolution of the reaction has been studied, then the results are compared with a scattering model suggested by Noremberg. A theoretical calculation based on both classical and statistical approaches giving the total cross-sections for any exit channel has been proposed

  19. Experimental study of bound states in $^{12}$Be through low-energy $^{11}$Be($d,p$)-transfer reactions

    CERN Document Server

    Johansen, J G; Borge, M J G; Cubero, M; Diriken, J; Elsevier, J; Fraile, L M; Fynbo, H O U; Gaffney, L P; Gernhäuser, R; Jonson, B; Koldste, G T; Konki, J; Kröll, T; Krücken, R; Mücher, D; Nilsson, T; Nowak, K; Pakarinen, J; Pesudo, V; Raabe, R; Riisager, K; Seidlitz, M; Tengblad, O; Törnqvist, H; Voulot, D; Warr, N; Wenander, F; Wimmer, K; De Witte, H

    2013-01-01

    The bound states of $^{12}$Be have been studied through a $^{11}$Be$(d,p)^{12}$Be transfer reaction experiment in inverse kinematics. A 2.8 MeV/u beam of $^{11}$Be was produced using the REX-ISOLDE facility at CERN. The outgoing protons were detected with the T-REX silicon detector array. The MINIBALL germanium array was used to detect $\\gamma$-rays from the excited states in $^{12}$Be. The $\\gamma$-ray detection enabled a clear identification of the four known bound states in $^{12}$Be, and each of the states has been studied individually. Differential cross sections over a large angular range have been extracted. Spectroscopic factors for each of the states have been determined from DWBA calculations and have been compared to previous experimental and theoretical results.

  20. Factors Controlling the Reactivity and Selectivity of the Diels-Alder Reactions Involving 1,2-Azaborines.

    Science.gov (United States)

    García-Rodeja, Yago; Fernández, Israel

    2016-08-01

    The factors controlling the reactivity and endo/exo selectivity of the Diels-Alder reactions involving 1,2-azaborines have been computationally explored within the density functional theory framework. It is found that the AlCl3-catalyzed [4 + 2]-cycloaddition reaction between these dienes and N-methylmaleimide proceeds concertedly and leads almost exclusively to the corresponding endo cycloadduct, which is in good agreement with previous experimental observations. In addition, the effect of the substituent directly attached to the boron atom of the 1,2-azaborine on the process is also analyzed in detail. To this end, the combination of the activation strain model of reactivity and the energy decomposition analysis methods has been applied to gain a quantitative understanding into the origins of the endo selectivity of the process as well as the influence of the boron and nitrogen substituent on the barrier heights of the transformations. PMID:27383907

  1. CsxH3-xPW12O40 heteropoly salts catalyzed quinoline synthesis via Friedlander reaction

    Institute of Scientific and Technical Information of China (English)

    Ezzat Rafiee; Fereshte Khajooei Nejad; Mohammad Joshaghani

    2011-01-01

    Various type of cesium partially substituted phosphotungstate, CsxH3-xPW12O40 (x = 1.0, 2.0 and 2.5), were synthesized and their catalytic activities were investigated in the synthesis of quinoline. It was shown that catalytic activities of these catalysts correlated to surface acidity and total number of acidic sites. Finally, a series of quinoline derivatives were synthesized with Cs2.5H0.5PW12O40 via the Friedlander reaction in high to excellent yields and the plausible mechanism was proposed. Simple experiment, catalyst reusability, short reaction time and preclusion of toxic solvent are the advantages of this method.

  2. Comparison of Reactors for Oxygen-Sensitive Reactions: Reductive Dechlorination of Chlorophenols by Vitamin B12s

    OpenAIRE

    Smith, Mark H.; Woods, Sandra L.

    1994-01-01

    Serum bottles are frequently used for studies of reductive dechlorination by vitamin B12, but reducing conditions can be maintained only for several days. This time period is inadequate for evaluating the reductive dechlorination of some slow-reacting aromatic compounds. Sealed glass ampoules maintain reducing conditions for many months, but this method has the disadvantage of disallowing subsampling of the reaction mixture. A glass serum tube was modified for these experiments which not only...

  3. BUU calculations for {sup 12}C+{sup 26}Mg reaction at 6-11 MeV/u

    Energy Technology Data Exchange (ETDEWEB)

    Kicinska-Habior, M. [Warsaw Univ., Inst. of Experimental Physics, Nuclear Physics Div., Warsaw (Poland)]|[Washington Univ., Nuclear Physics Lab., Seattle, WA (United States); Trznadel, Z. [Warsaw Univ., Inst. of Experimental Physics, Nuclear Physics Div., Warsaw (Poland); Snover, K.A.; Kelly, M.P. [Washington Univ., Nuclear Physics Lab., Seattle, WA (United States); Maj, A. [Washington Univ., Nuclear Physics Lab., Seattle, WA (United States)]|[Inst. of Nuclear Physics, Cracow (Poland)

    1997-12-31

    High energy gamma spectra measured in the {sup 12}C +{sup 26}Mg reaction at energies of 5, 8.5 and 11 MeV/u have been analysed using the BUU computer code (cascade model). In the calculation the statistical and nonstatistical gamma-ray emission as well as the Bremsstrahlung have been taken into account. The parameters of the Giant Dipole Resonance have been extracted. 4 refs, 1 fig., 2 tabs.

  4. Nano-Scale Au Supported on Carbon Materials for the Low Temperature Water Gas Shift (WGS Reaction

    Directory of Open Access Journals (Sweden)

    Paula Sánchez

    2011-12-01

    Full Text Available Au-based catalysts supported on carbon materials with different structures such as graphite (G and fishbone type carbon nanofibers (CNF-F were prepared using two different methods (impregnation and gold-sol to be tested in the water gas shift (WGS reaction. Atomic absorption spectrometry, transmission electron microscopy (TEM, temperature-programmed oxidation (TPO, X-ray diffraction (XRD, Raman spectroscopy, elemental analyses (CNH, N2 adsorption-desorption analysis, temperature-programmed reduction (TPR and temperature-programmed decomposition were employed to characterize both the supports and catalysts. Both the crystalline nature of the carbon supports and the method of gold incorporation had a strong influence on the way in which Au particles were deposited on the carbon surface. The higher crystallinity and the smaller and well dispersed Au particle size were, the higher activity of the catalysts in the WGS reaction was noted. Finally, catalytic activity showed an important dependence on the reaction temperature and steam-to-CO molar ratio.

  5. Energy loss of /sup 12/C projectiles in different carbon modifications

    International Nuclear Information System (INIS)

    The stopping cross sections of the three carbon modifications diamond, graphite, and glassy carbon are investigated for carbon projectiles of intermediate velocity. The inverted Doppler-shift attenuation method was used as the experimental technique, and it enabled us to measure the ratios of the three stopping cross sections precisely over a wide energy range. For velocities between 3 and 4 times Bohr's velocity the stopping cross sections of graphite and glassy carbon are found to be 1.036 and 1.072 times larger than that of diamond, respectively. These differences are attributed to binding effects. To understand these effects, we have evaluated the mean ionization potentials utilizing the local-plasma approximation for the inner-shell electrons and the dielectric response function for the valence electrons. The theoretical ratios calculated by inserting these potentials into the Bethe-Bloch stopping-power formula agree well with our experimental results. Furthermore, we have obtained a value of 53.3 +- 4.1 fs for the lifetime of the first excited state of the /sup 12/C nucleus

  6. Synthesis of magnetic Pb/Fe304/Si02 and its catalytic activity for propylene carbonate synthesis via urea and 1,2-propylene glycol

    Institute of Scientific and Technical Information of China (English)

    Hualiang AN; Xinqiang ZHAO; Zhiguang JIA; Changcheng WU; Yanji WANG

    2009-01-01

    To facilitate the recovery of Pb/SiO2 catalyst, magnetic Pb/Fe3O4/SiO2 samples were prepared separately by emulsification, sol-gel and incipient impregnation methods. The catalyst samples were characterized by means of X-ray diffraction and N2 adsorption-desorption, and their catalytic activity was investigated in the reaction for synthesizing propylene carbonate from urea and 1,2-propylene glycol. When the gelatin was applied in the preparation of Fe3O4 at 60°C and the pH value was controlled at 4 in the preparation of Fe3O4/SiO2, the Pb/ Fe3O4/SiO2 sample shows good catalytic activity and magnetism. Under the reaction conditions of a reaction temperature of 180°C, reaction time of 2 h, catalyst percentage of 1.7 wt-% and a molar ratio of urea to PG of 1:4, the yield of propylene carbonate attained was 87.7%.

  7. Accelerated carbonation using municipal solid waste incinerator bottom ash and cold-rolling wastewater: Performance evaluation and reaction kinetics.

    Science.gov (United States)

    Chang, E-E; Pan, Shu-Yuan; Yang, Liuhanzi; Chen, Yi-Hung; Kim, Hyunook; Chiang, Pen-Chi

    2015-09-01

    Accelerated carbonation of alkaline wastes including municipal solid waste incinerator bottom ash (MSWI-BA) and the cold-rolling wastewater (CRW) was investigated for carbon dioxide (CO2) fixation under different operating conditions, i.e., reaction time, CO2 concentration, liquid-to-solid ratio, particle size, and CO2 flow rate. The MSWI-BA before and after carbonation process were analyzed by the thermogravimetry and differential scanning calorimetry, X-ray diffraction, and scanning electron microscopy equipped with energy dispersive X-ray spectroscopy. The MSWI-BA exhibits a high carbonation conversion of 90.7%, corresponding to a CO2 fixation capacity of 102g perkg of ash. Meanwhile, the carbonation kinetics was evaluated by the shrinking core model. In addition, the effect of different operating parameters on carbonation conversion of MSWI-BA was statistically evaluated by response surface methodology (RSM) using experimental data to predict the maximum carbonation conversion. Furthermore, the amount of CO2 reduction and energy consumption for operating the proposed process in refuse incinerator were estimated. Capsule abstract: CO2 fixation process by alkaline wastes including bottom ash and cold-rolling wastewater was developed, which should be a viable method due to high conversion.

  8. Formation of brown carbon via reactions of ammonia with secondary organic aerosols from biogenic and anthropogenic precursors

    Science.gov (United States)

    Updyke, Katelyn M.; Nguyen, Tran B.; Nizkorodov, Sergey A.

    2012-12-01

    Filter samples of secondary organic aerosols (SOA) generated from the ozone (O3)- and hydroxyl radical (OH)-initiated oxidation of various biogenic (isoprene, α-pinene, limonene, α-cedrene, α-humulene, farnesene, pine leaf essential oils, cedar leaf essential oils) and anthropogenic (tetradecane, 1,3,5-trimethylbenzene, naphthalene) precursors were exposed to humid air containing approximately 100 ppb of gaseous ammonia (NH3). Reactions of SOA compounds with NH3 resulted in production of light-absorbing "brown carbon" compounds, with the extent of browning ranging from no observable change (isoprene SOA) to visible change in color (limonene SOA). The aqueous phase reactions with dissolved ammonium (NH4+) salts, such as ammonium sulfate, were equally efficient in producing brown carbon. Wavelength-dependent mass absorption coefficients (MAC) of the aged SOA were quantified by extracting known amounts of SOA material in methanol and recording its UV/Vis absorption spectra. For a given precursor, the OH-generated SOA had systematically lower MAC compared to the O3-generated SOA. The highest MAC values, for brown carbon from SOA resulting from O3 oxidation of limonene and sesquiterpenes, were comparable to MAC values for biomass burning particles but considerably smaller than MAC values for black carbon aerosols. The NH3/NH4+ + SOA brown carbon aerosol may contribute to aerosol optical density in regions with elevated concentrations of NH3 or ammonium sulfate and high photochemical activity.

  9. Highly Efficient Electrocatalysts for Oxygen Reduction Reaction Based on 1D Ternary Doped Porous Carbons Derived from Carbon Nanotube Directed Conjugated Microporous Polymers

    KAUST Repository

    He, Yafei

    2016-10-11

    © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.One-dimensional (1D) porous materials have shown great potential for gas storage and separation, sensing, energy storage, and conversion. However, the controlled approach for preparation of 1D porous materials, especially porous organic materials, still remains a great challenge due to the poor dispersibility and solution processability of the porous materials. Here, carbon nanotube (CNT) templated 1D conjugated microporous polymers (CMPs) are prepared using a layer-by-layer method. As-prepared CMPs possess high specific surface areas of up to 623 m2 g-1 and exhibit strong electronic interactions between p-type CMPs and n-type CNTs. The CMPs are used as precursors to produce heteroatom-doped 1D porous carbons through direct pyrolysis. As-produced ternary heteroatom-doped (B/N/S) 1D porous carbons possess high specific surface areas of up to 750 m2 g-1, hierarchical porous structures, and excellent electrochemical-catalytic performance for oxygen reduction reaction. Both of the diffusion-limited current density (4.4 mA cm-2) and electron transfer number (n = 3.8) for three-layered 1D porous carbons are superior to those for random 1D porous carbon. These results demonstrate that layered and core-shell type 1D CMPs and related heteroatom-doped 1D porous carbons can be rationally designed and controlled prepared for high performance energy-related applications.

  10. Magnetic Carbon Supported Palladium Nanoparticles: An Efficient and Sustainable Catalyst for Hydrogenation Reactions

    Science.gov (United States)

    Magnetic carbon supported Pd catalyst has been synthesized via in situ generation of nanoferrites and incorporation of carbon from renewable cellulose via calcination; the catalyst can be used for the hydrogenation of alkenes and reduction of aryl nitro compounds.

  11. Accelerated carbonation using municipal solid waste incinerator bottom ash and cold-rolling wastewater: Performance evaluation and reaction kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Chang, E-E [Department of Biochemistry, Taipei Medical University, 250 Wu-Hsing Street, Taipei City, Taiwan 110, Taiwan, ROC (China); Pan, Shu-Yuan [Graduate Institute of Environmental Engineering, National Taiwan University, 71 Chou-Shan Rd., Taipei City, Taiwan 10673, Taiwan, ROC (China); Yang, Liuhanzi [School of Environment, Tsinghua University, Haidin District, Beijing 100084 (China); Chen, Yi-Hung [Department of Chemical Engineering and Biotechnology, National Taipei University of Technology, 1, Sec. 3, Zhongxiao E. Rd., Taipei City, Taiwan 10608, Taiwan, ROC (China); Kim, Hyunook [Department of Energy and Environmental System Engineering, University of Seoul (Korea, Republic of); Chiang, Pen-Chi, E-mail: pcchiang@ntu.edu.tw [Graduate Institute of Environmental Engineering, National Taiwan University, 71 Chou-Shan Rd., Taipei City, Taiwan 10673, Taiwan, ROC (China)

    2015-09-15

    Highlights: • Carbonation was performed using CO{sub 2}, wastewater and bottom ash in a slurry reactor. • A maximum capture capacity of 102 g CO{sub 2} per kg BA was achieved at mild conditions. • A maximum carbonation conversion of MSWI-BA was predicted to be 95% by RSM. • The CO{sub 2} emission from Bali incinerator could be expected to reduce by 6480 ton/y. • The process energy consumption per ton CO{sub 2} captured was estimated to be 180 kW h. - Abstract: Accelerated carbonation of alkaline wastes including municipal solid waste incinerator bottom ash (MSWI-BA) and the cold-rolling wastewater (CRW) was investigated for carbon dioxide (CO{sub 2}) fixation under different operating conditions, i.e., reaction time, CO{sub 2} concentration, liquid-to-solid ratio, particle size, and CO{sub 2} flow rate. The MSWI-BA before and after carbonation process were analyzed by the thermogravimetry and differential scanning calorimetry, X-ray diffraction, and scanning electron microscopy equipped with energy dispersive X-ray spectroscopy. The MSWI-BA exhibits a high carbonation conversion of 90.7%, corresponding to a CO{sub 2} fixation capacity of 102 g per kg of ash. Meanwhile, the carbonation kinetics was evaluated by the shrinking core model. In addition, the effect of different operating parameters on carbonation conversion of MSWI-BA was statistically evaluated by response surface methodology (RSM) using experimental data to predict the maximum carbonation conversion. Furthermore, the amount of CO{sub 2} reduction and energy consumption for operating the proposed process in refuse incinerator were estimated. Capsule abstract: CO{sub 2} fixation process by alkaline wastes including bottom ash and cold-rolling wastewater was developed, which should be a viable method due to high conversion.

  12. Boron Doped Multi-walled Carbon Nanotubes as Catalysts for Oxygen Reduction Reaction and Oxygen Evolution Reactionin in Alkaline Media

    International Nuclear Information System (INIS)

    The boron doped multi-walled carbon nanotubes (B-MWCNTs) were synthesized by thermal annealing multi-walled carbon nanotubes (MWCNTs) in the presence of boric acid. The transmission electron microscopy (TEM) and X-ray diffraction (XRD) results revealed that the structure of MWCNTs does not be destroyed during the doping process, and X-ray photoelectron spectroscopy (XPS) analysis demonstrated the boron atoms were successfully doped in the structure of MWCNTs. The electrocatalytic properties of B-MWCNTs are characterized by rotating disk electrode (RDE) methods. The results demonstrated that the B-MWCNTs catalyzed oxygen reduction reaction (ORR) in alkaline media by a 2 + 2 electron pathway and it showed good catalytic activity for oxygen evolution reaction (OER) as well

  13. Carboxyl functionalization of carbon fibers via aryl diazonium reaction in molten urea to enhance interfacial shear strength

    Science.gov (United States)

    Wang, Yuwei; Meng, Linghui; Fan, Liquan; Wu, Guangshun; Ma, Lichun; Zhao, Min; Huang, Yudong

    2016-01-01

    Using molten urea as the solvent, carbon fibers were functionalized with carboxylic acid groups via aryl diazonium reaction in 15 min to improve their interfacial bonding with epoxy resin. The surface functionalization was quantified by X-ray photoelectron spectroscopy, which showed that the relative surface coverage of carboxylic acid groups increased from an initial percentage of 3.17-10.41%. Mechanical property test results indicated that the aryl diazonium reaction in this paper could improve the interfacial shear strength by 66%. Meanwhile, the technique did not adopt any pre-oxidation step to produce functional groups prior to grafting and was shown to maintain the tensile strength of the fibers. This methodology provided a rapid, facile and economically viable route to produce covalently functionalized carbon fibers in large quantities with an eco-friendly method.

  14. Low temperature synthesis of high quality carbon nanospheres through the chemical reactions between calcium carbide and oxalic acid

    Energy Technology Data Exchange (ETDEWEB)

    Xie Yonggui, E-mail: xieyg2004@163.com [State Key Laboratory for Powder Metallurgy, Central South University, Changsha, Hunan 410083 (China); Huang Qizhong, E-mail: qzhuang@mail.csu.edu.cn [State Key Laboratory for Powder Metallurgy, Central South University, Changsha, Hunan 410083 (China); Huang Baiyun [State Key Laboratory for Powder Metallurgy, Central South University, Changsha, Hunan 410083 (China); Xie Xiangmin [Applied Chemistry Department, College of Science, Hunan Agricultural University, Changsha, Hunan 410128 (China)

    2010-11-01

    Carbon nanospheres (CNSs) were synthesized through the chemical reactions of calcium carbide and oxalic acid without using catalysts. The chemical reactions were carried out in a sealed stainless steel pressure vessel with various molar ratios at temperatures of 65-250 deg. C. The synthesized CNSs have been characterized using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) attached to the SEM, transmission electron microscopy (TEM), X-ray diffraction (XRD) and Raman spectroscopy. The total yield of carbonaceous materials relative to the starting material is about 4% (w/w). SEM and TEM results reveal that the percentage of CNSs is high (>95%). The CNSs that have been synthesized are roe-like spheres of relatively uniform size with diameters of 60-120 nm. The attached EDS result shows that the carbon content of CNSs reaches up to 98%.

  15. Original Reaction Sequence of Pb(Yb1/2Nb1/2O3-PbTiO3: Consequences on Dielectric Properties and Chemical Order

    Directory of Open Access Journals (Sweden)

    Charlotte Cochard

    2015-01-01

    Full Text Available The solid solution [Pb(Yb1/2Nb1/2O3]1−x-[PbTiO3]x was synthesized with x≤60%, using several high-temperature techniques as well as room-temperature mechanosynthesis. The high-temperature synthesis reveals a reaction path involving the synthesis first of the end-members before the solid solution. The density and dielectric constant measured on the ceramics prepared from these powders indicate the crucial role of the synthesis technique in the subsequent properties. Mechanosynthesis results in ceramics with higher density and dielectric constant. Identical optimized sintering conditions were then applied to all investigated compositions and the resulting dielectric properties and chemical orders were compared. All polar orders (antiferroelectricity, ferroelectricity, and relaxor behavior were evidenced. The 1 : 1 chemical order on the B-site of Pb(Yb1/2Nb1/2O3 results in the formation of a double perovskite Pb2YbNbO6, and the superstructures in the X-ray diagrams signing the existence of this order persist up to 30% PbTiO3. The underlying mechanism for substitution of Yb or Nb by Ti is presented.

  16. Synthesis of graphitic carbon nitride by reaction of melamine and uric acid

    Energy Technology Data Exchange (ETDEWEB)

    Dante, Roberto C., E-mail: rcdante@yahoo.com [Laboratorio de Tecnologias del Medio Ambiente, Departamento de Ingenieria Agricola y Forestal, Universidad de Valladolid, Avenida de Madrid 44, 34004 Palencia (Spain); Martin-Ramos, Pablo, E-mail: pablomartinramos@gmail.com [Laboratorio de Tecnologias del Medio Ambiente, Departamento de Ingenieria Agricola y Forestal, Universidad de Valladolid, Avenida de Madrid 44, 34004 Palencia (Spain); Correa-Guimaraes, Adriana, E-mail: acg@iaf.uva.es [Laboratorio de Tecnologias del Medio Ambiente, Departamento de Ingenieria Agricola y Forestal, Universidad de Valladolid, Avenida de Madrid 44, 34004 Palencia (Spain); Martin-Gil, Jesus, E-mail: jesusmartingil@gmail.com [Laboratorio de Tecnologias del Medio Ambiente, Departamento de Ingenieria Agricola y Forestal, Universidad de Valladolid, Avenida de Madrid 44, 34004 Palencia (Spain)

    2011-11-01

    Highlights: {yields} Graphitic carbon nitrides by CVD of melamine and uric acid on alumina. {yields} The building blocks of carbon nitrides are heptazine nuclei. {yields} Composite particles with alumina core and carbon nitride coating. - Abstract: Graphitic carbon nitrides were synthesized starting from melamine and uric acid. Uric acid was chosen because it thermally decomposes, and reacts with melamine by condensation at temperatures in the range of 400-600 deg. C. The reagents were mixed with alumina and subsequently the samples were treated in an oven under nitrogen flux. Alumina favored the deposition of the graphitic carbon nitrides layers on the exposed surface. This method can be assimilated to an in situ chemical vapor deposition (CVD). Infrared (IR) spectra, as well as X-ray diffraction (XRD) patterns, are in accordance with the formation of a graphitic carbon nitride with a structure based on heptazine blocks. These carbon nitrides exhibit poor crystallinity and a nanometric texture, as shown by transmission electron microscopy (TEM) analysis. The thermal degradation of the graphitic carbon nitride occurs through cyano group formation, and involves the bridging tertiary nitrogen and the bonded carbon, which belongs to the heptazine ring, causing the ring opening and the consequent network destruction as inferred by connecting the IR and X-ray photoelectron spectroscopy (XPS) results. This seems to be an easy and promising route to synthesize graphitic carbon nitrides. Our final material is a composite made of an alumina core covered by carbon nitride layers.

  17. Carbon Fibre and Its Reaction With Metals%碳纤维及其与金属的作用

    Institute of Scientific and Technical Information of China (English)

    赵浩峰; 王玲; 刘红梅; 韩世平

    2001-01-01

    本文介绍了金属基复合材料中常用增强物——碳纤维的结构及性能,特别总结讨论了碳纤维与常用金属的结合类型。%The paper deals with the structure and performance of carbon fibre used in MMCs and especially the reaction between it and some metals.

  18. Dynamics of surface-migration: Electron-induced reaction of 1,2-dihaloethanes on Si(100)

    Science.gov (United States)

    Huang, Kai; MacLean, Oliver; Guo, Si Yue; McNab, Iain R.; Ning, Zhanyu; Wang, Chen-Guang; Ji, Wei; Polanyi, John C.

    2016-10-01

    Scanning Tunneling Microscopy was used to investigate the electron-induced reaction of 1,2-dibromoethane (DBE) and 1,2-dichloroethane (DCE) on Si(100).We observed a long-lived physisorbed molecular state of DBE at 75 K and of DCE at 110 K. As a result we were able to characterize by experiment and also by ab initio theory the dynamics of ethylene production in the electron-induced surface-reaction of these physisorbed species. For both DBE and DCE the ethylene product was observed to migrate across the surface. In the case of DBE the recoil of the ethylene favored the silicon rows, migrating by an average distance of 22 Å, and up to 100 Å. Trajectory calculations were performed for this electron-induced reaction, using an 'Impulsive Two-State' model involving an anionic excited state and a neutral ground-potential. The model agreed with experiment in reproducing both migration and desorption of the ethylene product. The computed migration exhibited a 'ballistic' launch and subsequent 'bounces', thereby accounting for the observed long-range migratory dynamics.

  19. Protective effect of application of carbon nanoparticles in thyroid cancer surgery and evaluation of inflammatory stress reaction degree

    Institute of Scientific and Technical Information of China (English)

    Qing-Sheng Zheng; Jun-Zheng Li; Wei-Xiong Hong; Jiao-Yuan Xu; Si-Yi Zhang

    2015-01-01

    Objective:To study the protective effect of application of carbon nanoparticles in thyroid cancer surgery and its influence on inflammatory stress reaction degree.Methods:Patients who received thyroid cancer surgery in our hospital from June 2013 to June 2014 were chosen for study and randomly divided into conventional group and nano-carbon group. Then contents of thyroid cancer related malignant molecules, pro-inflammation cytokines and inflammation inhibiting factors in serum were detected.Results:(1) Malignant molecules: compared with conventional group, mRNA levels of Wip1, gal-3, SATB1, LSD1, GDF-15 and TBX2 in serum of nano-carbon group were lower; (2) Inflammation inhibiting factors: compared with conventional group, serum MFG-E8 and Omentin-1 levels of nano-carbon group were higher; (3) Pro-inflammation cytokines: compared with conventional group, serum MIP-1, SGK-1 and β-EP levels of nano-carbon group were lower.Conclusion: Application of carbon nanoparticles in thyroid cancer surgery is helpful to reduce operative damage to thyroid tissue, prevent release of malignant biological molecules into bloodstream and relieve inflammatory response; it’s an ideal surgical method for thyroid cancer.

  20. Effect of carbon content on microstructure and mechanical properties of hot-rolled low carbon 12Cr-Ni stainless steel

    International Nuclear Information System (INIS)

    Research highlights: → Hot-rolled ultra low carbon martensite is characterized by dislocation cells substructure. → The formation of dislocation cells is attributed to high Ms and low interstitial atoms content. → Hot-rolled ultra low carbon 12Cr-Ni stainless steel has excellent impact toughness. → Delta ferrite deteriorates the impact toughness of hot-rolled 12Cr-Ni stainless steel. - Abstract: 12Cr-Ni stainless steels containing different carbon contents from 0.004 wt.% to 0.034 wt.% were hot-rolled and air-cooled. Their corresponding microstructures were observed with optical microscope and transmission electron microscope, and the Vickers hardness, tensile and impact tests were also carried out. It was found that the martensitic morphology was significantly influenced by carbon content. The as-received ultra low carbon martensite in the steel containing 0.004 wt.% C is characterized by dislocation cells substructure. The formation of dislocation cells is attributed to high martensite finishing point (above 400 deg. C) and low interstitial atoms content. On the other hand, the martensite in the steel containing 0.034 wt.% C consists mainly of typical martensite laths because of low martensite finishing point and high interstitial atoms content which hinder dislocation motion. Furthermore, carbon content has an evident effect on the mechanical properties of 12Cr-Ni steels. The hardness and strength of the as-received steels increase with an increase in carbon content, but their elongation and impact toughness decrease with the carbon content. The steel containing 0.004 wt.% C has excellent impact toughness due to the ultra low carbon content in the martensite composed of dislocation cells.

  1. Electrocatalytic oxygen evolution reaction at a FeNi composite on a carbon nanofiber matrix in alkaline media

    Institute of Scientific and Technical Information of China (English)

    Xianghua An; Dongyoon Shin; Joey D. Ocon; Jae Kwang Lee; Young-il Son; Jaeyoung Lee

    2014-01-01

    Non-noble metals such as Fe and Ni have comparable electrocatalytic activity and stability to that of Ir and Ru in an oxygen evolution reaction (OER). In this study, we synthesized carbon nanofibers with embedded FeNi composites (FeNi-CNFs) as OER electrocatalysts by a facile route comprising electrospinning and the pyrolysis of a mixture of metal precursors and a polymer solution. FeNi-CNFs demonstrated catalytic activity and stability that were better than that of 20 wt%Ir on Vulcan carbon black in oxidizing water to produce oxygen in an alkaline media. Physicochemical and electrochemical characterization revealed that Fe and Ni had synergistic roles that enhanced OER activity by the uniform formation and widening of pores in the carbon structure, while the CNF matrix also contributed to the increased stability of the catalyst.

  2. Study of the Nuclear Transparency in $\\alpha$ + A Reactions at Energies $\\geq$ 12 GeV/nucleon

    CERN Multimedia

    2002-01-01

    The question about transparency is crucial for heavy ion reaction studies. If the transparency is low at 10-15 GeV per nucleon then very large baryon densities can be achieved in this energy range, maybe enough to produce quark-gluon plasma in U+U collisions. We propose to measure, event by event, pseudo-rapidity and multiplicity distributions of singly charged relativistic particles (@b~$>$~0.7) globally and in selected regions of rapidity as well as multiplicities of recoiling protons (30-400~Me charged nuclear fragments. These studies will explore general features of @a+A reactions at energies @$>$~12~GeV/nucleon. The main goal of the experiment is to measure the transparency of nuclear matter in this energy range. The detector will be nuclear emulsion.

  3. A photochemical model for the carbon-rich planet WASP-12b

    CERN Document Server

    Kopparapu, Ravi kumar; Zahnle, Kevin J

    2011-01-01

    The hot Jupiter WASP-12b is a heavily irradiated exoplanet in a short period orbit around a G0-star with twice the metallicity of the Sun. A recent thermochemical equilibrium analysis based on Spitzer and ground-based infrared observations suggests that the presence of $\\ch4$ in its atmosphere and the lack of $\\h2o$ features can only be explained if the carbon-to-oxygen ratio in the planet's atmosphere is much greater than the solar ratio ($\\ctoo = 0.54$). Here, we use a 1-D photochemical model to study the effect of disequilibrium chemistry on the observed abundances of $\\h2o, \\com, \\co2$ and $\\ch4$ in the WASP-12b atmosphere. We consider two cases: one with solar $\\ctoo$ and another with $\\ctoo = 1.08$. The solar case predicts that $\\h2o$ and $\\com$ are more abundant than $\\co2$ and $\\ch4$, as expected, whereas the high $\\ctoo$ model shows that $\\com$, C$_{2}$H$_{2}$ and HCN are more abundant. This indicates that the extra carbon from the high $\\ctoo$ model is in hydrocarbon species. $\\h2o$ photolysis is th...

  4. Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.

    Science.gov (United States)

    Ghorai, Manas K; Halder, Sandipan; Das, Subhomoy

    2015-10-01

    A simple strategy for the synthesis of highly functionalized cyclohexanone derivatives containing an all-carbon quaternary center from α-(aryl/alkyl)methylidene-β-keto esters or β-diketones via a K-enolate mediated domino Michael-Michael reaction sequence with moderate to good yield and excellent diastereoselectivity (de > 99%) is described. Interestingly, Li-base mediated reaction of α-arylmethylidene-β-diketones affords functionalized 3,5-dihydroxy cyclohexane derivatives as the kinetically controlled products via a domino aldol-aldol reaction sequence with excellent diastereoselectivity. Li-enolates of the β-keto esters or β-diketones undergo facile domino Michael-Michael reaction with nitro-olefins to afford the corresponding nitrocyclohexane derivatives in good yields and excellent diastereoselectivity (de > 99%). The formation of the products and the observed stereoselectivity were explained by plausible mechanisms and supported by extensive computational study. An asymmetric version of the protocol was explored with (L)-menthol derived nonracemic substrates, and the corresponding nonracemic cyclohexanone derivatives containing an all-carbon quaternary center were obtained with excellent stereoselectivity (de, ee > 99%).

  5. Study of 12Be using the 11Be(9Be,8Be) transfer reaction at TRIUMF ISAC-II

    Science.gov (United States)

    Braid, Ryan; Sarazin, Fred; TIGRESS Collaboration; (PCB)2 Collaboration

    2015-10-01

    Recent results at TRIUMF and NSCL have called into question the structure of 12Be, therefore another look at this nucleus is desirable. The structure is important information for theoretical models, since it constrains the mechanism that produces parity inversion in 11Be. The 12Be structure was probed in July 2014 using the (PCB)2 array (Printed Circuit Board Based Charged Particle) inside TIGRESS (TRIUMF - ISAC Gamma Ray Escape Suppressed Spectrometer) at TRIUMF using the 11Be(9Be,8Be)12Be reaction at 55 MeV in inverse kinematics. A second set of data at 30 MeV was collected. This reaction has numerous advantages over the traditional (d,p) method, foremost of which is the 8Be --> 2 α breakup since it allows for very clean identification and tagging. Additionally, TIGRESS will allow precise γ-tagging for the excited states. The initial data and analysis will be presented in this talk. This work is partially supported by the US Department of Energy through Grant/Contract No. DE-FG03-93ER40789 (Colorado School of Mines).

  6. Comparing carbon nanotubes and graphene nanoplatelets as reinforcements in polyamide 12 composites

    Science.gov (United States)

    Chatterjee, S.; Nüesch, F. A.; Chu, B. T. T.

    2011-07-01

    We investigate the influence of nanofillers including carbon nanotubes (CNTs) and graphene nanoplatelets on a thermoplastic engineering polymer, polyamide 12 (PA12). The comparison between these two important nanofillers as to how they influence the structure and properties of the polymer is systematically studied. The polymer-nanofiller composites were prepared using a twin-screw micro-extruder and the composite was thereafter hot pressed into thin films. The structure (using wide angle x-ray diffraction and differential scanning calorimetry) and properties (through tensile testing and conductivity measurement) of the thin films have been investigated. The composites incorporating surfactant showed the best CNT distribution and dispersion, causing an improvement of up to 80% in the toughness modulus over pure PA12. Electrical percolation could also be achieved at nanofiller concentrations of 1 to 2 wt%. In this study we observed that CNT fillers bring about more pronounced improvements in PA12 compared to graphene nanoplatelets, as far as mechanical and electrical properties are concerned.

  7. Comparing carbon nanotubes and graphene nanoplatelets as reinforcements in polyamide 12 composites

    Energy Technology Data Exchange (ETDEWEB)

    Chatterjee, S; Nueesch, F A; Chu, B T T, E-mail: bryan.chu@empa.ch [EMPA, Laboratory for Functional Polymers, Swiss Federal Laboratories for Materials Science and Technology (Switzerland)

    2011-07-08

    We investigate the influence of nanofillers including carbon nanotubes (CNTs) and graphene nanoplatelets on a thermoplastic engineering polymer, polyamide 12 (PA12). The comparison between these two important nanofillers as to how they influence the structure and properties of the polymer is systematically studied. The polymer-nanofiller composites were prepared using a twin-screw micro-extruder and the composite was thereafter hot pressed into thin films. The structure (using wide angle x-ray diffraction and differential scanning calorimetry) and properties (through tensile testing and conductivity measurement) of the thin films have been investigated. The composites incorporating surfactant showed the best CNT distribution and dispersion, causing an improvement of up to 80% in the toughness modulus over pure PA12. Electrical percolation could also be achieved at nanofiller concentrations of 1 to 2 wt%. In this study we observed that CNT fillers bring about more pronounced improvements in PA12 compared to graphene nanoplatelets, as far as mechanical and electrical properties are concerned.

  8. Enhanced electrochemical performance of Li4Ti5O12 as anode material for lithium-ion batteries with different carbons as support

    International Nuclear Information System (INIS)

    Nano-Li4Ti5O12/carbon composites with various structures are designed using tetrabutyl titanate as a precursor via a facile in situ liquid deposition method in the presence of three different carbons (multiwalled carbon nanotubes, spherical conductive carbon black super-P and ordered macroporous carbon). The nano-Li4Ti5O12/carbon composites with various morphologies are formed depending on the carbon matrixes used. The Li4Ti5O12 particles obtained are approximately 100 nm in size and homogeneously dispersed in different carbon matrixes. It is found that the structures of the carbon matrixes have a close relation to the discharge capacities of the composites. At the discharge current density of 875 mA g−1, the discharge capacities of nano-Li4Ti5O12/carbon composites with 10 wt% carbon are 138.6, 120.8 and 120.9 mAh g−1 for carbon nanotubes, super-P and porous carbon as the carbon supports, respectively. The nano-Li4Ti5O12/carbon using carbon nanotubes as support exhibits superior performance with large reversible capacity, excellent cycle stability and good rate capability. Capacity retention of 99% can be maintained after 100 cycles, suggesting its promising potential as anode materials. - Highlights: • Li4Ti5O12/carbon nanocomposites are designed using different carbons as supports. • Li4Ti5O12 particles formed on carbon matrix are fine and homogeneous. • Aggregation and growth of Li4Ti5O12 particles are inhibited. • The Li4Ti5O12/carbon nanocomposites exhibit superior electrochemical performance

  9. Carbon doped molybdenum disulfide nanosheets stabilized on graphene for the hydrogen evolution reaction with high electrocatalytic ability

    Science.gov (United States)

    Li, Yong; Wang, Jiao; Tian, Xike; Ma, Longlong; Dai, Chu; Yang, Chao; Zhou, Zhaoxin

    2016-01-01

    Fabricating a cost effective hydrogen evolution reaction catalyst without using precious metal elements is in crucial demand for environmentally-benign energy production. In this work, the thin and edge-rich molybdenum disulfide nanosheets, with carbon doped in the interlayers and decorated on graphene, were developed by a facile solvothermal process. The as-synthesized nanohybrids exhibited high catalytic ability for the hydrogen evolution electrochemical reaction with an onset overpotential of 0.165 mV and a Tafel slope of 46 mV dec-1. Furthermore, the prepared nanohybrids also showed better durability and stability. Our work may lead to a potential method for in situ production of metal carbide-sulphur hybrid nanomaterials with promising applications for the hydrogen evolution reaction.Fabricating a cost effective hydrogen evolution reaction catalyst without using precious metal elements is in crucial demand for environmentally-benign energy production. In this work, the thin and edge-rich molybdenum disulfide nanosheets, with carbon doped in the interlayers and decorated on graphene, were developed by a facile solvothermal process. The as-synthesized nanohybrids exhibited high catalytic ability for the hydrogen evolution electrochemical reaction with an onset overpotential of 0.165 mV and a Tafel slope of 46 mV dec-1. Furthermore, the prepared nanohybrids also showed better durability and stability. Our work may lead to a potential method for in situ production of metal carbide-sulphur hybrid nanomaterials with promising applications for the hydrogen evolution reaction. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr07370g

  10. Study and realization of heavy ion detectors. Application to the reaction 12C+24Mg

    International Nuclear Information System (INIS)

    The present study deals with elastic and inelastic scattering of 24 to 44 MeV center of mass 24Mg ions by 12C. The Strasbourg Q3D magnetic spectrograph has been used to measure the 1800 c.m. scattering cross-sections in detecting the corresponding recoiling ions at THETAsub(Lab) = 00. Statistical fluctuations are probably present. The 1,5 m long position sensitive focal plan hybride counter is described

  11. Transition metal/nitrogen dual-doped mesoporous graphene-like carbon nanosheets for the oxygen reduction and evolution reactions

    Science.gov (United States)

    Liu, Xiaobo; Amiinu, Ibrahim Saana; Liu, Shaojun; Cheng, Kun; Mu, Shichun

    2016-07-01

    The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) have been considered as a key step in energy conversion processes. Here, a novel and simple Mg(OH)2 nanocasting method is adopted to fabricate Co and N co-doped porous graphene-like carbon nanosheets (Co@N-PGCS) by using chitosan as both carbon and N sources. The as-obtained Co@N-PGCS shows a mesopore-dominated structure as well as a high specific surface area (1716 cm2 g-1). As a bifunctional electrocatalyst towards both the ORR and OER, it shows favorable ORR performance compared with the commercial Pt/C catalyst with an onset potential of -0.075 V and a half-wave potential of -0.151 V in 0.1 M KOH solutions. Furthermore, it also displays considerable OER properties compared with commercial IrO2. The effective catalytic activity could originate from the introduction of transition metal species and few-layer mesoporous carbon structures.The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) have been considered as a key step in energy conversion processes. Here, a novel and simple Mg(OH)2 nanocasting method is adopted to fabricate Co and N co-doped porous graphene-like carbon nanosheets (Co@N-PGCS) by using chitosan as both carbon and N sources. The as-obtained Co@N-PGCS shows a mesopore-dominated structure as well as a high specific surface area (1716 cm2 g-1). As a bifunctional electrocatalyst towards both the ORR and OER, it shows favorable ORR performance compared with the commercial Pt/C catalyst with an onset potential of -0.075 V and a half-wave potential of -0.151 V in 0.1 M KOH solutions. Furthermore, it also displays considerable OER properties compared with commercial IrO2. The effective catalytic activity could originate from the introduction of transition metal species and few-layer mesoporous carbon structures. Electronic supplementary information (ESI) available: The XPS fitted results, SEM and TEM images, the K-L equation, and some of the electrochemical

  12. Measurement of 4He(12C,16O)γ Reaction in Inverse Kinematics

    International Nuclear Information System (INIS)

    A cross section measurement employing a direct 16O detection method for the reaction energies from Ecm = 2.4 to 0.7 MeV is planned at Kyushu University Tandem Laboratory. To perform this experiment and to obtain quantitative information about the cross section to within an error of 10%, we have developed several instruments, including a blow-in type windowless gas target and a ionization chamber. A target thickness of 24 × 3.9 Torr cm was achieved using the developed gas target. The particle identification was successfully performed by using the energy deposit in the ionization chamber. Experiments were performed at Ecm = 2.4 and 1.5 MeV using the developed instruments and the cross sections were obtained. (author)

  13. Chrystal structure properties of Al-doped Li4Ti5O12 synthesized by solid state reaction method

    Science.gov (United States)

    Sandi, Dianisa Khoirum; Priyono, Slamet; Suryana, Risa

    2016-02-01

    This research aim is to analyze the effect of Aluminum (Al) doping in the structural properties of Al-doped Li4Ti5O12 as anode in lithium ion battery. Al-doped Li4Ti5O12 powders were synthesized by solid state reaction method. LiOH.H2O, TiO2, and Al2O3 were raw materials. These materials were milled for 15 h, calcined at temperature of 750oC and sintered at temperature of 800oC. Mole percentage of doping Al (x) was varied at x=0; x=0.025; and x =0.05. Al-doped Li4Ti5O12 powders were synthesized by solid state reaction method. X-ray diffraction was employed to determine the structure of Li4Ti5O12. The PDXL software was performed on the x-ray diffraction data to estimate the phase percentage, the lattice parameter, the unit cell volume, and the crystal density. Al-doped Li4Ti5O12 has cubic crystal structure. Al-doping at x=0 and x=0.025 does not change the phase as Li4Ti5O12 while at x=0.050 the phase changes to the LiTiAlO4. The diffraction patterns show that the angle shifted to the right as the increase of x which indicated that Al substitute Ti site. Percentage of Li4Ti5O12 phase at x=0 and x=0.025 was 97.8% and 96.8%, respectively. However, the lattice parameters, the unit cell volume, and the crystal density does not change significantly at x=0; x=0.025; and x=0.050. Based on the percentage of Li4Ti5O12 phase, the Al-doped Li at x=0 and x=0.025 is promising as a lithium battery anode.

  14. The pp → pp π+π- reaction at primary impulses of 12 and 24 GeV/c

    International Nuclear Information System (INIS)

    The author has studied the pp → ppπ+π- reaction at primary impulses of 12 to 24 GeV/c. He has obtained the mass spectra of the pπ+π- system which show evidence for diffractive production of a N*(1470) resonance together with superpositions of further resonance-like structures. Furthermore the decay of the pπ+π- system is studied by means of a momentum analysis of the decay angular distributions. Finally a partial wave analysis is performed. (HSI)

  15. Study of Reaction Mechanism in the Interaction 86 MeV/A $^{12}$C with Heavy Targets

    CERN Multimedia

    2002-01-01

    Using the thin target-thin catcher techniques and the off-line analysis of the activities induced in the irradiated foils by means of singles and coincidences spectra recorded with Ge(Li) @g-rays and Si X-rays detectors, we will measure: 1) The target fragment mass and charge distribution from the interact 2) 86 MeV/A |1|2C with silver, tin and gold. 3) The target fragment average kinetic energy. 4) The target fragment angular and differential kinetic energy distributions. These measurements should allow us to better understand the heavy ion reaction mechanisms at intermediate energy.

  16. Dispersion quality of amine functionalized multiwall carbon nanotubes plays critical roles in polymerase chain reaction enhancement

    Energy Technology Data Exchange (ETDEWEB)

    Yuce, Meral, E-mail: meralyuce@sabanciuniv.edu; Budak, Hikmet [Sabanci University, Nanotechnology Research and Application Centre (Turkey)

    2014-12-15

    Impact of dispersion quality of NH{sub 2}-MWCNTs (13–18 nm in diameter with a length between 1 and 12 µm, >99 % purity) in the amplification efficiency of a random DNA oligonucleotide library (96 bp) was investigated. Amplification yield in the presence of non-filtered NH{sub 2}-MWCNT dispersion, filtered NH{sub 2}-MWCNT dispersion and surface-attached NH{sub 2}-MWCNTs was explored, and physical interactions between NH{sub 2}-MWCNTs and major PCR reagents including DNA template, wild type Taq DNA polymerase enzyme and primers were determined using high resolution polyacrylamide gel electrophoresis, dynamic light scattering, UV–Vis-NIR spectroscopy and scanning electron microscopy techniques. The results revealed that presence of NH{sub 2}-MWCNT dispersion which was sonicated, centrifuged and filtered, enhanced the total PCR efficiency up to 70 % while the presence of NH{sub 2}-MWCNT only centrifuged after sonication, inhibited the reaction significantly at similar concentrations. Furthermore, the NH{sub 2}-MWCNTs coupled covalently onto magnetic microspheres, contributed for the specificity enhancement whilst decreasing the amplification efficiency by 30 % at the maximum concentration, which suggests a removable enhancement system for sensitive applications. On the other hand, the relative hydrodynamic size distribution measurements displayed a clear difference between the filtered NH{sub 2} and non-filtered NH{sub 2}-MWCNT water dispersions, which justifies the inhibition of the amplification by the non-filtered NH{sub 2}-MWCNTs containing big agglomerates and bundles. Finally, we demonstrated that major PCR components adsorb onto the NH{sub 2}-MWCNTs with diverse affinities, and maintain their functions after adsorption, which provides a good framework to further develop tunable NH{sub 2}-MWCNT-carriers to be utilized in various nanobiotechnology and material science applications.

  17. 40 CFR 600.510-12 - Calculation of average fuel economy and average carbon-related exhaust emissions.

    Science.gov (United States)

    2010-07-01

    ... must meet the minimum driving range requirements established by the Secretary of Transportation (49 CFR... 40 Protection of Environment 29 2010-07-01 2010-07-01 false Calculation of average fuel economy and average carbon-related exhaust emissions. 600.510-12 Section 600.510-12 Protection of...

  18. Photochemical Reaction of 7,12-Dimethylbenz[a]anthracene (DMBA and Formation of DNA Covalent Adducts

    Directory of Open Access Journals (Sweden)

    Peter P. Fu

    2005-04-01

    Full Text Available DMBA, 7,12-dimethylbenz[a]anthracene, is a widely studied polycyclic aromatic hydrocarbon that has long been recognized as a probable human carcinogen. It has been found that DMBA is phototoxic in bacteria as well as in animal or human cells and photomutagenic in Salmonella typhimurium strain TA102. This article tempts to explain the photochemistry and photomutagenicity mechanism. Light irradiation converts DMBA into several photoproducts including benz[a]anthracene-7,12-dione, 7-hydroxy-12-keto-7-methylbenz[a]anthracene, 7,12-epidioxy-7,12-dihydro-DMBA, 7-hydroxymethyl-12-methylbenz[a]anthracene and 12-hydroxymethyl-7-methylbenz[a]anthracene. Structures of these photoproducts have been identified by either comparison with authentic samples or by NMR/MS. At least four other photoproducts need to be assigned. Photo-irradiation of DMBA in the presence of calf thymus DNA was similarly conducted and light-induced DMBA-DNA adducts were analyzed by 32P-postlabeling/TLC, which indicates that multiple DNA adducts were formed. This indicates that formation of DNA adducts might be the source of photomutagenicity of DMBA. Metabolites obtained from the metabolism of DMBA by rat liver microsomes were reacted with calf thymus DNA and the resulting DNA adducts were analyzed by 32P-postlabeling/TLC under identical conditions. Comparison of the DNA adduct profiles indicates that the DNA adducts formed from photo-irradiation are different from the DNA adducts formed due to the reaction of DMBA metabolites with DNA. These results suggest that photo-irradiation of DMBA can lead to genotoxicity through activation pathways different from those by microsomal metabolism of DMBA.

  19. Metal-Carbon Hybrid Electrocatalysts Derived from Ion-Exchange Resin Containing Heavy Metals for Efficient Hydrogen Evolution Reaction.

    Science.gov (United States)

    Zhou, Yucheng; Zhou, Weijia; Hou, Dongman; Li, Guoqiang; Wan, Jinquan; Feng, Chunhua; Tang, Zhenghua; Chen, Shaowei

    2016-05-01

    Transition metal-carbon hybrids have been proposed as efficient electrocatalysts for hydrogen evolution reaction (HER) in acidic media. Herein, effective HER electrocatalysts based on metal-carbon composites are prepared by controlled pyrolysis of resin containing a variety of heavy metals. For the first time, Cr2 O3 nanoparticles of 3-6 nm in diameter homogeneously dispersed in the resulting porous carbon framework (Cr-C hybrid) is synthesized as efficient HER electrocatalyst. Electrochemical measurements show that Cr-C hybrids display a high HER activity with an onset potential of -49 mV (vs reversible hydrogen electrode), a Tafel slope of 90 mV dec(-1) , a large catalytic current density of 10 mA cm(-2) at -123 mV, and the prominent electrochemical durability. X-ray photoelectron spectroscopic measurements confirm that electron transfer occurs from Cr2 O3 into carbon, which is consistent with the reported metal@carbon systems. The obtained correlation between metals and HER activities may be exploited as a rational guideline in the design and engineering of HER electrocatalysts. PMID:27061759

  20. Designing nitrogen-enriched echinus-like carbon capsules for highly efficient oxygen reduction reaction and lithium ion storage.

    Science.gov (United States)

    Hu, Chuangang; Wang, Lixia; Zhao, Yang; Ye, Minhui; Chen, Qing; Feng, Zhihai; Qu, Liangti

    2014-07-21

    Both structural and compositional modulations are important for high-performance electrode materials in energy conversion/storage devices. Here hierarchical-structure nitrogen-rich hybrid porous carbon capsules with bamboo-like carbon nanotube whiskers (N-CC@CNTs) grown in situ have been specifically designed, which combine the advantageous features of high surface area, abundant active sites, easy access to medium and favorable mass transport. As a result, the newly prepared N-CC@CNTs show highly efficient catalytic activity in oxygen reduction reaction in alkaline media for fuel cells, which not only outperforms commercial Pt-based catalysts in terms of kinetic limiting current, stability and tolerance to methanol crossover effect, but is also better than most of the nanostructured carbon-based catalysts reported previously. On the other hand, as an anode material for lithium ion batteries, the N-CC@CNTs obtained also exhibit an excellent reversible capacity of ca. 1337 mA h g(-1) at 0.5 A g(-1), outstanding rate capability and long cycling stability, even at a current density of 20 A g(-1). The capacity is the highest among all the heteroatom-doped carbon materials reported so far, and is even higher than that of many of the composites of metal, metal oxides or metal sulfides with carbon materials. PMID:24906180

  1. The chemistry of subcritical water reactions of a hardwood derived lignin and lignin model compounds with nitrogen, hydrogen, carbon monoxide and carbon dioxide

    Science.gov (United States)

    Hill Bembenic, Meredith A.

    collected solids from the CO reactions appeared to be the most reacted (i.e., the most changed from the unreacted lignin) according to solid state 13C-NMR analysis, and the widest variety of products (methoxy-substituted phenolic compounds) were obtained when using CO according to GC/MS analysis. Therefore, reactions with CO were completed that varied the initial reaction pressure (300, 500 and 800 psi) in order to elucidate the effects of CO pressure. Similar conversion (≈54--58%) and DCM-soluble liquid product yields (≈53--62%) were obtained for the different pressure reactions, but the reactions with an initial pressure of 500 psi had the greatest change in aromaticity from the unreacted lignin. Additional reactions between Organosolv lignin and H2O with CO (initial pressure of 500 psi) were conducted where the reaction time was varied (15, 30 and 60 min.) to determine the effect of reaction time. Longer reaction time (60 min.) appeared to inhibit conversion to low molecular weight compounds (i.e., conversion and DCM-soluble yields were lower at ≈53% and ≈28%, respectively). Solid state 13C-NMR of collected residues also showed that there are losses in carbons representative of both guaiacyl and syringyl components as reaction time increases, which may indicate that methoxy groups are being cleaved or the products are reacting with each other (i.e., repolymerization) to form high molecular weight compounds as reaction time is increased. The role of H2O and the gases during the baseline reactions and the expanded CO reactions is not intuitive based on the results, so reactions with lignin model compounds (i.e., aromatic aldehydes represented by vanillin and syringaldehyde, aromatic ketones represented by acetovanillone and acetosyringone, and aromatic ethers represented by dibenzyl ether and 2-phenethyl phenyl ether) were completed to study this. From these results, the suggested reaction pathway of Organosolv lignin reactions in subcritical H2O with and without

  2. Wastage-resistant characteristics of 12Cr steel tube material. Small leak sodium-water reaction test

    International Nuclear Information System (INIS)

    In the water leak accident of a steam generator designed for a sodium cooled reactor in the Feasibility Study, the localization of tube failure propagation by using an advanced water leak detector will be required from the viewpoints of the safety and economical efficiency of the plant. So far, the conventional knowledge and analytical tools have been used in the investigation and evaluation of water leak phenomenon; nevertheless, there was neither test data nor the study of quantitative evaluation on the corrosion behavior, so-called wastage-resistant characteristics, of 12Cr steel tube material in sodium-water reactions. Wastage tests for the 12Cr steel tube material were conducted in small water leaks by use of the Sodium-Water Reaction Test Rig (SWAT-1R), and the data of wastage rate were obtained in the parameter of water leak rate under the constant sodium temperature and distance between leak and target tubes. The test results lead to the following conclusions: (1) The wastage-resistibility of 12Cr steel is 1.6 times greater than that of 9Cr steel and is 2.7 times greater than that of 2.25Cr-1Mo steel. (2)The wastage-resistibility of 12Cr steel increases in smaller water leaks; especially in water leak rates of 1 g/sec or less, it is more excellent than that of SUS321 stainless steel used as Monju superheater tube material. (3) Based on the correlation of wastage rate for the 9Cr steel, the correlation for the 12Cr steel has been obtained to be used for the evaluation of tube failure propagation. As the correlation of wastage rate for the 12Cr steel is based on the correlation for the 9Cr steel, it gives enough conservatism in smaller water leaks. To serve in accurately evaluating the tube failure propagation in smaller water leaks, it is necessary to obtain new correlation of wastage rate for the 12Cr steel based on the data in the wide range of water leak rates. (author)

  3. Antioxidants Inhibit Formation of 3-Monochloropropane-1,2-diol Esters in Model Reactions.

    Science.gov (United States)

    Li, Chang; Jia, Hanbing; Shen, Mingyue; Wang, Yuting; Nie, Shaoping; Chen, Yi; Zhou, Yongqiang; Wang, Yuanxing; Xie, Mingyong

    2015-11-11

    The capacities of six antioxidants to inhibit the formation of 3-monochloropropane-1,2 diol (3-MCPD) esters were examined in this study. Inhibitory capacities of the antioxidants were investigated both in chemical models containing the precursors (tripalmitoyl glycerol, 1,2-dipalmitoyl-sn-glycerol, monopalmitoyl glycerol, and sodium chloride) of 3-MCPD esters and in oil models (rapeseed oil and sodium chloride). Six antioxidants, butylated hydroxytoluene (BHT), butylated hydroxy anisole (BHA), tert-butyl hydroquinone (TBHQ), propyl gallate (PG), L-ascorbyl palmitate (AP), and α-tocopherol (VE), were found to exhibit inhibiting capacities on 3-MCPD ester formation both in chemical models and in oil models. TBHQ provided the highest inhibitory capacity both in chemical models and in oil models; 44% of 3-MCPD ester formation was inhibited in the presence of TBHQ (66 mg/kg of oil) after heating of rapeseed oil at 230 °C for 30 min, followed by PG and AP. BHT, BHA, and VE appeared to have weaker inhibitory abilities in both models. VE exhibited the lowest inhibition rate; 22% of 3-MCPD esters were inhibited in the presence of VE (172 mg/kg of oil) after heating of rapeseed oil at 230 °C for 30 min. In addition, the inhibition rates of PG and VE decreased dramatically with an increase in temperature or heating time. The results suggested that some antioxidants, such as TBHQ, PG, and AP, could be the potential inhibitors of 3-MCPD esters in practice. PMID:26478126

  4. Cobalt nanoparticles embedded in N-doped carbon as an efficient bifunctional electrocatalyst for oxygen reduction and evolution reactions

    Science.gov (United States)

    Su, Yunhe; Zhu, Yihua; Jiang, Hongliang; Shen, Jianhua; Yang, Xiaoling; Zou, Wenjian; Chen, Jianding; Li, Chunzhong

    2014-11-01

    Cobalt based catalysts are promising bifunctional electrocatalysts for both oxygen reduction and oxygen evolution reactions (ORR and OER) in unitized regenerative fuel cells (URFCs) operating with alkaline electrolytes. Here we report a hybrid composite of cobalt nanoparticles embedded in nitrogen-doped carbon (Co/N-C) via a solvothermal carbonization strategy. With the synergistic effect arising from the N-doped carbon and cobalt nanoparticles in the composite, the Co/N-C hybrid catalyst exhibits highly efficient bifunctional catalytic activity and excellent stability toward both ORR and OER. The ΔE (oxygen electrode activity parameter for judging the overall electrocatalytic activity of a bifunctional electrocatalyst) value for Co/N-C is 0.859 V, which is smaller than those of Pt/C and most of the non-precious metal catalysts in previous studies. Furthermore, the Co/N-C composite also shows better bifunctional catalytic activity than its oxidative counterparts, which could be attributed to the high specific surface area and the efficient charge transfer ability of the composite, as well as the good synergistic effect between N-doped carbon and the Co nanoparticles in the Co/N-C composite.Cobalt based catalysts are promising bifunctional electrocatalysts for both oxygen reduction and oxygen evolution reactions (ORR and OER) in unitized regenerative fuel cells (URFCs) operating with alkaline electrolytes. Here we report a hybrid composite of cobalt nanoparticles embedded in nitrogen-doped carbon (Co/N-C) via a solvothermal carbonization strategy. With the synergistic effect arising from the N-doped carbon and cobalt nanoparticles in the composite, the Co/N-C hybrid catalyst exhibits highly efficient bifunctional catalytic activity and excellent stability toward both ORR and OER. The ΔE (oxygen electrode activity parameter for judging the overall electrocatalytic activity of a bifunctional electrocatalyst) value for Co/N-C is 0.859 V, which is smaller than those

  5. Nitrogen-Doped Carbon Nanoparticle-Carbon Nanofiber Composite as an Efficient Metal-Free Cathode Catalyst for Oxygen Reduction Reaction.

    Science.gov (United States)

    Panomsuwan, Gasidit; Saito, Nagahiro; Ishizaki, Takahiro

    2016-03-23

    Metal-free nitrogen-doped carbon materials are currently considered at the forefront of potential alternative cathode catalysts for the oxygen reduction reaction (ORR) in fuel cell technology. Despite numerous efforts in this area over the past decade, rational design and development of a new catalyst system based on nitrogen-doped carbon materials via an innovative approach still present intriguing challenges in ORR catalysis research. Herein, a new kind of nitrogen-doped carbon nanoparticle-carbon nanofiber (NCNP-CNF) composite with highly efficient and stable ORR catalytic activity has been developed via a new approach assisted by a solution plasma process. The integration of NCNPs and CNFs by the solution plasma process can lead to a unique morphological feature and modify physicochemical properties. The NCNP-CNF composite exhibits a significantly enhanced ORR activity through a dominant four-electron pathway in an alkaline solution. The enhancement in ORR activity of NCNP-CNF composite can be attributed to the synergistic effects of good electron transport from highly graphitized CNFs as well as abundance of exposed catalytic sites and meso/macroporosity from NCNPs. More importantly, NCNP-CNF composite reveals excellent long-term durability and high tolerance to methanol crossover compared with those of a commercial 20 wt % supported on Vulcan XC-72. We expect that NCNP-CNF composite prepared by this synthetic approach can be a promising metal-free cathode catalyst candidate for ORR in fuel cells and metal-air batteries. PMID:26908214

  6. Flow characteristics and reaction properties of carbon dioxide in microtubules and porous media

    Institute of Scientific and Technical Information of China (English)

    ZHAO RenBao; YUE XiangAn; WU Ya Hong; XU ShaoLiang; WANG Fei; HOU YongLi

    2008-01-01

    Carbon dioxide reacts with porous media while flowing through them enhancing their permeability. Its flow behavior as well as the permeability enhancement effects were studied in synthetic cores, natural cores and microtubes with an inner diameter of 5 μm. The results show that the permeability of H2O-saturated cores (containing carbonate ingredients) was enhanced by increasing the injection volume of a CO2-H2O solution. This enhancement is attributable to carbon dioxide's corrosion, which is justified by SEM scanning. The same phenomenon occurs with a CO2-H2O solution in microtubes, but for a different reason. The gas flow velocity of carbon dioxide in microtubes was approximately 100% aster than that of nitrogen because of the scale and the squeezing effects. Carbon dioxide molecules dissolved in water accelerate the diffusion rate of water molecules within the boundary layer, which in turn diminishes the thickness of the water film and enlarges the effective pore size. This flow behavior facilitates the injection of carbon dioxide into low-permeability reservoirs for oil-displacement and formation energy buildup purposes. This behavior also increases the potential for carbon dioxide channeling or release from the formation.

  7. Graphite Carbon-Supported Mo2C Nanocomposites by a Single-Step Solid State Reaction for Electrochemical Oxygen Reduction.

    Directory of Open Access Journals (Sweden)

    K Huang

    Full Text Available Novel graphite-molybdenum carbide nanocomposites (G-Mo2C are synthesized by a typical solid state reaction with melamine and MoO3 as precursors under inert atmosphere. The characterization results indicate that G-Mo2C composites are composed of high crystallization and purity of Mo2C and few layers of graphite carbon. Mo2C nanoparticles with sizes ranging from 5 to 50 nm are uniformly supported by surrounding graphite layers. It is believed that Mo atom resulting from the reduction of MoO3 is beneficial to the immobilization of graphite carbon. Moreover, the electrocatalytic performances of G-Mo2C for ORR in alkaline medium are investigated by cyclic voltammetry (CV, rotating disk electrode (RDE and chronoamperometry test with 3M methanol. The results show that G-Mo2C has a considerable catalytic activity and superior methanol tolerance performance for the oxygen reduction reaction (ORR benefiting from the chemical interaction between the carbide nanoparticles and graphite carbon.

  8. Graphite Carbon-Supported Mo2C Nanocomposites by a Single-Step Solid State Reaction for Electrochemical Oxygen Reduction.

    Science.gov (United States)

    Huang, K; Bi, K; Liang, C; Lin, S; Wang, W J; Yang, T Z; Liu, J; Zhang, R; Fan, D Y; Wang, Y G; Lei, M

    2015-01-01

    Novel graphite-molybdenum carbide nanocomposites (G-Mo2C) are synthesized by a typical solid state reaction with melamine and MoO3 as precursors under inert atmosphere. The characterization results indicate that G-Mo2C composites are composed of high crystallization and purity of Mo2C and few layers of graphite carbon. Mo2C nanoparticles with sizes ranging from 5 to 50 nm are uniformly supported by surrounding graphite layers. It is believed that Mo atom resulting from the reduction of MoO3 is beneficial to the immobilization of graphite carbon. Moreover, the electrocatalytic performances of G-Mo2C for ORR in alkaline medium are investigated by cyclic voltammetry (CV), rotating disk electrode (RDE) and chronoamperometry test with 3M methanol. The results show that G-Mo2C has a considerable catalytic activity and superior methanol tolerance performance for the oxygen reduction reaction (ORR) benefiting from the chemical interaction between the carbide nanoparticles and graphite carbon.

  9. Nitrogen-doped carbon-embedded TiO2 nanofibers as promising oxygen reduction reaction electrocatalysts

    Science.gov (United States)

    Hassen, D.; Shenashen, M. A.; El-Safty, S. A.; Selim, M. M.; Isago, H.; Elmarakbi, A.; El-Safty, A.; Yamaguchi, H.

    2016-10-01

    The development of inexpensive and effective electrocatalysts for oxygen reduction reaction (ORR) as a substitute for commercial Pt/C catalyst is an important issue in fuel cells. In this paper, we report on novel fabrication of self-supported nitrogen-doped carbon-supported titanium nanofibers (Nsbnd TiO2@C) and carbon-supported titanium (TiO2@C) electrocatalysts via a facile electrospinning route. The nitrogen atom integrates physically and homogenously into the entire carbon-titanium structure. We demonstrate the catalytic performance of Nsbnd TiO2@C and TiO2@C for ORR under alkaline conditions in comparison with Pt/C catalyst. The Nsbnd TiO2@C catalyst shows excellent ORR reactivity and durability. Interestingly, among all the catalysts used in this ORR, Nsbnd TiO2@C-0.75 exhibits remarkable competitive oxygen reduction activity in terms of current density and onset potential, as well as superior methanol tolerance. Such tolerance attributes to maximizing the diffusion of trigger pulse electrons during catalytic reactions because of enhanced electronic features. Results indicate that our fabrication strategy can provide an opportunity to produce a simple, efficient, cost-effective, and promising ORR electrocatalyst for practical applications in energy conversion and storage technologies.

  10. Transition metal/nitrogen dual-doped mesoporous graphene-like carbon nanosheets for the oxygen reduction and evolution reactions.

    Science.gov (United States)

    Liu, Xiaobo; Amiinu, Ibrahim Saana; Liu, Shaojun; Cheng, Kun; Mu, Shichun

    2016-07-21

    The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) have been considered as a key step in energy conversion processes. Here, a novel and simple Mg(OH)2 nanocasting method is adopted to fabricate Co and N co-doped porous graphene-like carbon nanosheets (Co@N-PGCS) by using chitosan as both carbon and N sources. The as-obtained Co@N-PGCS shows a mesopore-dominated structure as well as a high specific surface area (1716 cm(2) g(-1)). As a bifunctional electrocatalyst towards both the ORR and OER, it shows favorable ORR performance compared with the commercial Pt/C catalyst with an onset potential of -0.075 V and a half-wave potential of -0.151 V in 0.1 M KOH solutions. Furthermore, it also displays considerable OER properties compared with commercial IrO2. The effective catalytic activity could originate from the introduction of transition metal species and few-layer mesoporous carbon structures. PMID:27341409

  11. Chemical behaviour of Pu and Am: Hydrolysis reaction in brine solutions, carbonate complexation, α-radiolysis, humate complexation and speciation

    International Nuclear Information System (INIS)

    The chemical behaviour of transuranic elements (Pu and Am) has been investigated in saline solution of different NaCl concentrations in the near neutral pH range. Important reactions considered are hydrolysis, carbonate complexation, redox reaction, alpha-radiolysis, colloid generation and humate complexation. Hydrolysis reactions are studied for Pu(VI) in 3.6 M NaCl and for Am(III) in 0.1 M and 0.6 M NaCl solution, whereas carbonate complexation of Pu(IV) and Am(III) is investigated in HCO3-/CO32- solution of varying pH. Consequences of alpha-radiolysis in NaCl solution are thoroughly analysed as for the Eh change due to Cl- oxidation and the oxidation of Pu(IV) and Am(III). In groundwaters colloid generation of Am(III), particularly pseudocolloids, is characterized and correlated with the concentration of humic substances. Humate complexation under discussion deals mainly with the stabilization of Am(III) in a given groundwater through its colloid generation. (orig.)

  12. Synthesis and infrared spectra of alkaline earth metal carbonates formed by the reaction of metal salts with urea at high temperature

    Indian Academy of Sciences (India)

    S M Teleb; D El-Sayed Nassr; E M Nour

    2004-12-01

    The metal carbonate, MCO3 (M = Ca, Sr and Ba), was synthesized by a novel method of reacting aqueous solution of each of Ca2+, Sr2+ and Ba2+ salts with urea at high temperature, ∼ 80°C. The reaction products were characterized through elemental analysis and infrared spectra. The infrared spectra of the products are the same as those of the corresponding commercially obtained carbonates. A general reaction describing the formation of MCO3 is proposed.

  13. 12 Years of NPK Addition Diminishes Carbon Sink Potential of a Nutrient Limited Peatland

    Science.gov (United States)

    Larmola, T.; Bubier, J. L.; Juutinen, S.; Moore, T. R.

    2011-12-01

    Peatlands store about a third of global soil carbon. Our aim was to study whether the vegetation feedbacks of nitrogen (N) deposition lead to stronger carbon sink or source in a nutrient limited peatland ecosystem. We investigated vegetation structure and ecosystem CO2 exchange at Mer Bleue Bog, Canada, that has been fertilized for 7-12 years. We have applied 5 and 20 times ambient annual wet N deposition (0.8 g N m-2) with or without phosphorus (P) and potassium (K). Gross photosynthesis, ecosystem respiration and net CO2 exchange (NEE) were measured weekly during the growing season using chamber technique. Under the highest N(PK) treatments, the light saturated photosynthesis (PSmax) was reduced by 20-30% compared to the control treatment, whereas under moderate N and PK additions PSmax slightly increased or was similar to the control. The ecosystem respiration showed similar trends among the treatments, but changes in the rates were less pronounced. High nutrient additions led to up to 65% lower net CO2 uptake than that in the control: In the NPK plots with cumulative N additions of 70, 19, and 0 g N m-2, the daytime NEE in May-July 2011 averaged 0.8 (se. 0.3), 2.0 (se. 0.4), and 2.4 (se. 0.3) μmol m-2 s-1, respectively. In the N only plots with cumulative N additions of 45, 19, and 0 g N m-2, the daytime NEE in May-July 2011 averaged 0.8 (se. 0.2), 2.6 (se. 0.4), and 1.8 (se. 0.3) μmol m-2 s-1, respectively. The reduced plant photosynthetic capacity and diminished carbon sink potential in the highest nutrient treatments correlated with the loss of peat mosses and were not compensated for by the increased vascular plant biomass that has mainly been allocated to woody shrub stems.

  14. Quasi-bound alpha resonant states populated by the {sup 12}C({sup 6}Li, d) reaction

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, M.R.D.; Borello-Lewin, T.; Miyake, H.; Horodynski-Matsushigue, L.B.; Duarte, J.L.M.; Rodrigues, C.L.; Souza, M.A. [Universidade de Sao Paulo (IF/USP), SP (Brazil). Inst. de Fisica; Cunsolo, A.; Cappuzzello, F.; Foti, A.; Agodi, C.; Cavallaro, M. [Istituto Nazionale di Fisica Nucleare (LNS/INFN), Catania (Italy). Lab. Nazionali del Sud; Ukita, G.M. [Universidade de Santo Amaro (UNISA), Sao Paulo, SP (Brazil). Faculdade de Psicologia

    2012-07-01

    Full text: The alpha cluster phenomenon in the light nuclei structure has been the subject of a long time investigation since the proposal of the Ikeda diagrams [1]. The main purpose of the research program in progress is the investigation of this phenomenon in (x{alpha}) and (x{alpha}+n) nuclei through the ({sup 6}Li, d) alpha transfer reaction [2-4]. Alpha resonant states around the (4{alpha}) threshold in the nucleus {sup 16}O are the focus of the present contribution. In fact, the importance of these resonances at the elements production in stars is recognized, as primarily pointed out by Hoyle in {sup 12}C [6]. The existence of a rotational band with the {alpha} +{sup 12} C (Hoyle) cluster state structure was recently demonstrated by Ohkubo and Hirabayashi [6]. In order to explore this region of interest, measurements of the {sup 12}C({sup 6}Li, d){sup 16}O reaction up to 17 MeV of excitation at an incident energy of 25.5 MeV, have been performed employing the Sao Paulo Pelletron-Enge Split-Pole facility and the nuclear emulsion detection technique (plates Fuji G6B, 50 {mu}m thick). Spectra associated with six scattering angles, from 5 deg to 29 deg in the laboratory frame, each one 50 cm along the focal surface, were measured. Several narrow resonances with a quasi-bound behavior embedded in the continuum were detected and the resolution of 25 keV allowed for the separation of doublets not resolved before [7,8]. The absolute cross sections and the respective deuteron angular distributions were determined and the analysis is in progress. [1] K. Ikeda et al., Prog. Theor. Phys. Suppl. E 68, 464 (1968); H. Horiuchi, K. Ikeda, and Y. Suzuki, ibid. 44, 225 (1978). [2] M.R.D.Rodrigues et al., in12th International Conference on Nuclear Reaction Mechanism, Varenna, Italy, edited by F. Cerutti and A. Ferrari , CERN Proceedings, 2010-2, pp. 331- 335. [3] T. Borello-Lewin et al., Proceedings of SOTANCP2, Brussels, Belgium 2010, edited by P. Descouvemount et al., Int. J

  15. Ion exchange reactions in interaction of basic zirconium sulfate with sodium carbonate solution

    International Nuclear Information System (INIS)

    Basic zirconium sulfates, extracted from basic zirconium chloride solution and zirconium disulfate solution, as well as products of their interaction with sodium carbonate solution, which was exposed and not exposed to hydrolysis, were investigated by chemical and NMR spectroscopy methods. It has been established that the process of interaction of the basic zirconium sulfate with sodium carbonate solutions sulfatocarbonatozicrconates and carbonatozirconates of sodium are sequentially formed. In this case carbonate groups, due to different strenght of addition of hydroxogroups in initial basic sulfates, substitute either SOsub(h)sup(2)-)- groups and H2O or SO42--and OH--groups, and sodium ions substitute H3O+-groups. Carbonate groups, if they have substituted sulfato- or hydroxogroup, during hydrolysis of carbonatozirconates are splitted out to a less degree

  16. On the water promoted reaction of titanium isopropoxide with carbon dioxide

    OpenAIRE

    Ghosh, Rajshekhar; Nethaji, Munirathinam; Samuelson, Ashoka G

    2003-01-01

    Insertion of carbon dioxide into titanium isopropoxide takes place only in the presence of trace quantities of water to give an isopropyl carbonato cluster which has been crystallographically characterised.

  17. Preparation of tantalum carbide films by reaction of electrolytic carbon coating with the tantalum substrate

    OpenAIRE

    Massot, Laurent; Chamelot, Pierre; Taxil, Pierre

    2006-01-01

    This article demonstrates that coatings of tantalum carbide can be obtained by electrodeposition of carbon in molten fluorides on a tantalum substrate as an alternative to the CVD process. The structural characteristics of the carbon deposited by the electrolytic route lead to a high reactivity of this element towards a tantalum cathode to produce tantalum carbide. Mutual reactivity was shown to be enhanced if tantalum plate is replaced by an electrodeposited layer of tantalum, where th...

  18. Study on the Reaction Mechanism for Carbon Dioxide Reforming of Methane over supported Nickel Catalyst

    Institute of Scientific and Technical Information of China (English)

    Ling QIAN; Zi Feng YAN

    2003-01-01

    The adsorption and dissociation of methane and carbon dioxide for reforming on nickelcatalyst were extensively investigated by TPSR and TPD experiments. It showed that thedecomposition of methane results in the formation of at least three kinds of surface carbon specieson supported nickel catalyst, while CO2 adsorbed on the catalyst weakly and only existed in onekind of adsorption state. Then the mechanism of interaction between the species dissociatedfrom CH4 and CO2 during reforming was proposed.

  19. $\\rho/\\omega$ properties from dilepton spectra in $p A$ reactions at 12 GeV

    CERN Document Server

    Bratkovskaya, E L

    2002-01-01

    The dilepton production from $pC$ and $pCu$ collisions at $T_{lab}=12$ GeV is calculated using the semi-classical BUU transport model, that includes the off-shell propagation of vector mesons nonperturbatively and calculates the width of the vector mesons dynamically. It is found that the collisional broadening of the vector meson width and dropping vector meson masses lead to a small enhancement of the dilepton yield below the $\\omega$ meson mass pole in $p Cu$ collisions compared to $p C$, which is, however, not sufficient to explain the enhanced production of dileptons as observed in the experiment by the KEK-PS E325 collaboration. It is argued that such in-medium effects are expected to be small due to kinematical reasons -- the dominant part of vector mesons shine dileptons and decay outside the nucleus due to the finite formation time for $\\rho$ and $\\omega$ mesons, which is large by Lorentz covariance since the produced vector mesons move with high velocity relative to the target nucleus.

  20. Short-range correlations in carbon-12, oxygen-16, and neon-20: Intrinsic properties

    Science.gov (United States)

    Braley, R. C.; Ford, W. F.; Becker, R. L.; Patterson, M. R.

    1972-01-01

    The Brueckner-Hartree-Fock (BHF) method has been applied to nuclei whose intrinsic structure is nonspherical. Reaction matrix elements were calculated as functions of starting energy for the Hamada-Johnston interaction using the Pauli operator appropriate to O-16 and a shifted oscillator spectrum for virtual excited states. Binding energies, single particle energies, radii, and shape deformations of the intrinsic state, in ordinary as well as renormalized BHF, are discussed and compared with previous HF studies and with experiment when possible. Results are presented for C-12, 0-16 and Ne-20. It is found that the binding energies and radii are too small, but that separation energies are well reproduced when the renormalized theory is used.

  1. A novel electrocatalyst for oxygen evolution reaction based on rational anchoring of cobalt carbonate hydroxide hydrate on multiwall carbon nanotubes

    Science.gov (United States)

    Zhang, Yuxia; Xiao, Qingqing; Guo, Xin; Zhang, Xiaoxue; Xue, Yifei; Jing, Lin; Zhai, Xue; Yan, Yi-Ming; Sun, Kening

    2015-03-01

    Cobalt carbonate hydroxide hydrate (CCHH) nanosheets have been densely and strongly anchored onto mildly oxidized multiwalled carbon nanotubes with the assistance of diethylenetriamine (DETA). The resulted hybrid (CCHH/MWCNT) is used as high efficient electrocatalyst for water oxidation with an extremely low onset potential of ∼1.47 V vs. RHE and an overpotential of 285 mV to achieve a current density of 10 mA cm-2 in 1.0 mol L-1 KOH. The CCHH/MWCNT electrode affords a Tafel slope of 51 mV/decade and an exchange current density of 2.5 × 10-7 A cm-2. Moreover, the CCHH/MWCNT catalyst delivers a high faradic efficiency of 95% and possesses remarkable stability for long-term electrolysis of water. By contrast, neither MWCNT nor CCHH exhibits apparent catalytical activity towards water oxidation. Importantly, we demonstrate that DETA plays crucial role in determining the morphology, structure of the CCHH/MWCNT, therefore resulting in an enhanced performance for water oxidation. This work not only provides a novel cobalt-based electrocatalyst for oxygen evolution, but also offers a useful and viable approach to deliberately synthesize functional nanocomposites for applications in energy conversion and storage.

  2. A Nodular Foreign Body Reaction in a Dialysis Patient Receiving Long-term Treatment With Lanthanum Carbonate.

    Science.gov (United States)

    Valika, Aziz K; Jain, Dhanpat; Jaffe, Phillip E; Moeckel, Gilbert; Brewster, Ursula C

    2016-01-01

    A 63-year-old man with HIV (human immunodeficiency virus) infection and end-stage renal disease, treated with lanthanum carbonate phosphate binder for 4 years, presented with anemia and an upper gastrointestinal bleed. Upper endoscopy revealed a nodular hyperplastic epithelium, with an endoscopic ultrasound confirming hyperechoic material within the nodules. Light microscopy showed collections of histiocytes and multinucleated giant cells containing brown granular cytoplasmic material and extracellular crystalline material, a finding confirmed by electron microscopy. Similar pathologic findings associated with lanthanum exposure have been described recently. In our patient, lanthanum carbonate treatment was withdrawn and gastrointestinal bleeding has since ceased. The patient was exposed to a high amount of lanthanum over a long period, which may explain his adverse reaction. However, other contributing factors, such as competing medications or comorbid conditions, also may have increased his sensitivity to the drug.

  3. Nitrogen-modified carbon-based catalysts for oxygen reduction reaction in polymer electrolyte membrane fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Subramanian, Nalini P.; Li, Xuguang; Nallathambi, Vijayadurda; Kumaraguru, Swaminatha P.; Colon-Mercado, Hector; Wu, Gang; Lee, Jong-Won; Popov, Branko N. [Center for Electrochemical Engineering, Department of Chemical Engineering, University of South Carolina, Columbia, SC 29208 (United States)

    2009-03-01

    Nitrogen-modified carbon-based catalysts for oxygen reduction were synthesized by modifying carbon black with nitrogen-containing organic precursors. The electrocatalytic properties of catalysts were studied as a function of surface pre-treatments, nitrogen and oxygen concentrations, and heat-treatment temperatures. On the optimum catalyst, the onset potential for oxygen reduction is approximately 0.76 V (NHE) and the amount of hydrogen peroxide produced at 0.5 V (NHE) is approximately 3% under our experimental conditions. The characterization studies indicated that pyridinic and graphitic (quaternary) nitrogens may act as active sites of catalysts for oxygen reduction reaction. In particular, pyridinic nitrogen, which possesses one lone pair of electrons in addition to the one electron donated to the conjugated {pi} bond, facilitates the reductive oxygen adsorption. (author)

  4. Evaluation of carbon-supported Pt and Pd nanoparticles for the hydrogen evolution reaction in PEM water electrolysers

    Science.gov (United States)

    Grigoriev, S. A.; Millet, P.; Fateev, V. N.

    Carbon-supported Pt and Pd nanoparticles (CSNs) were synthesized and electrochemically characterized in view of potential application in proton exchange membrane (PEM) water electrolysers. Electroactive metallic nanoparticles were obtained by chemical reduction of precursor salts adsorbed to the surface of Vulcan XC-72 carbon carrier, using ethylene glycol as initial reductant and with final addition of formaldehyde. CSNs were then coated over the surface of electron-conducting working electrodes using an alcoholic solution of perfluorinated polymer. Their electrocatalytic activities with regard to the hydrogen evolution reaction (HER) were measured in sulfuric acid solution using cyclic voltammetry, and in a PEM cell during water electrolysis. Results obtained show that palladium can be advantageously used as an alternative electrocatalyst to platinum for the HER in PEM water electrolysers. Developed electrocatalysts could also be used in PEM fuel cells.

  5. In situ catalyzed Boudouard reaction of coal char for solid oxide-based carbon fuel cells with improved performance

    International Nuclear Information System (INIS)

    Highlights: • Industrial coal char was used as a fuel for solid oxide-based carbon fuel cells. • The Boudouard reactivity of coal char is higher than that of a commercial activated carbon. • The mineral matter in coal char has a catalytic effect on the Boudouard reaction. • Added catalysts and the inherent catalysts synergetically improved cell output. - Abstract: The use of industrial coal char as a fuel source for an anode-supported solid oxide-based carbon fuel cell (SO-CFC) with a yttrium-stabilized zirconia electrolyte and La0.8Sr0.2MnO3 cathode was investigated. Both the Boudouard reactivity and electrochemical performance of the coal char samples are higher than those of activated carbon samples under the same conditions. The inherent catalytic activity of the metal species (FemOn, CaO, etc.) in the coal char mineral matter leads to good cell performance, even in the absence of an external catalyst. For example, the peak power density of a cell fueled with pure coal char is 100 mW cm−2 at 850 °C, and that of a cell fueled with coal char impregnated with an FemOn-alkaline metal oxide catalyst is 204 mW cm−2. These results suggest that using coal char as the fuel in SO-CFCs might be an attractive way to utilize abundant coal resources cleanly and efficiently, providing an alternative for future power generation

  6. Measurement of Fragment Production Cross Sections in the $^{12}$C+$^{12}$C and $^{12}$C+$^{197}$Au Reactions at 62 $A$ MeV for Hadrontherapy and Space Radiation Protection

    CERN Document Server

    Tropea, S; Agodi, C; Blancato, A A; Bondì, M; Cappuzzello, F; Carbone, D; Cavallaro, M; Cirrone, G A P; Cuttone, G; Giacoppo, F; Nicolosi, D; Pandola, L; Raciti, G; Rapisarda, E; Romano, F; Sardina, D; Scuderi, V; Sfienti, C

    2014-01-01

    Over the last twenty years, there has been a renewed interest in nuclear fragmentation studies for both hadrontherapy applications and space radiation protection. In both fields, fragmentation cross sections are needed to predict the effects of the ions nuclear interactions within the patient’s and the astronaut’s body. Indeed, the Monte Carlo codes used in planning tumor treatments and space missions must be tuned and validated by experimental data. However, only a limited set of fragmentation cross sections are available in literature, especially at Fermi energies. Therefore, we have studied the production of secondary fragments in the 12 C+ 12 C and 12 C+ 197 Au reactions at 62 A MeV. In this work, the measured 4 He cross sections angular distributions at four selected angles are presented and compared.

  7. Up-Scaling Geochemical Reaction Rates for Carbon Dioxide (CO2) in Deep Saline Aquifers

    Energy Technology Data Exchange (ETDEWEB)

    Lindquist, W Brent

    2009-03-03

    The overall goal of the project was to bridge the gap between our knowledge of small-scale geochemical reaction rates and reaction rates meaningful for modeling transport at core scales. The working hypothesis was that reaction rates, determined from laboratory measurements based upon reactions typically conducted in well mixed batch reactors using pulverized reactive media may be significantly changed in in situ porous media flow due to rock microstructure heterogeneity. Specifically we hypothesized that, generally, reactive mineral surfaces are not uniformly accessible to reactive fluids due to the random deposition of mineral grains and to the variation in flow rates within a pore network. Expected bulk reaction rates would therefore have to be correctly up-scaled to reflect such heterogeneity. The specific objective was to develop a computational tool that integrates existing measurement capabilities with pore-scale network models of fluid flow and reactive transport. The existing measurement capabilities to be integrated consisted of (a) pore space morphology, (b) rock mineralogy, and (c) geochemical reaction rates. The objective was accomplished by: (1) characterizing sedimentary sandstone rock morphology using X-ray computed microtomography, (2) mapping rock mineralogy using back-scattered electron microscopy (BSE), X-ray dispersive spectroscopy (EDX) and CMT, (3) characterizing pore-accessible reactive mineral surface area, and (4) creating network models to model acidic CO{sub 2} saturated brine injection into the sandstone rock samples.

  8. Synthesis and properties of novel aliphatic polycarbonate from carbon dioxide with 1,2-butylene oxide and ε-caprolactone

    Institute of Scientific and Technical Information of China (English)

    Yan Fei Liu; Ke Long Huang; Dong Ming Peng; Su Qin Liu; Hong Wu

    2007-01-01

    A new degradable aliphatic poly(butylene-co-ε-caprolactone carbonate) (PBCL) was synthesized through the terpolymerization of carbon dioxide, 1,2-butylene oxide (BO) and ε-caprolactone (CL), a polymer supported bimetallic complex (PBM) was used as a catalyst. The terpolymers prepared were characterized by FT-IR, 1H NMR, 13C NMR, WXRD and DSC. The hydrolysis tests were carried out to appraise the degradability of the copolymers.

  9. Suppression of interfacial reactions between Li4Ti5O12 electrode and electrolyte solution via zinc oxide coating

    International Nuclear Information System (INIS)

    Graphical abstract: The Li4Ti5O12 (LTO) based batteries have severe gassing behavior due to the strong interfacial reactions between LTO and the electrolyte solution, which hampers the practical application of LTO in high power LIBs. The ZnO coating on LTO particles as a barrier layer can effectively suppress the interfacial reactions between LTO and the electrolyte solution. Simultaneously, the ZnO coating significantly reduces the charge-transfer resistance and increases the lithium ion diffusion coefficient, which leads to great improvement of rate and cyclic performance of LTO electrode. - Highlights: • A ZnO coating layer was constructed on the LTO particles by a chemical process as a barrier layer between LTO and surrounding electrolyte solution. • The ZnO coating can effectively stabilize the electrode/electrolyte interface and suppress interfacial reactions between LTO and electrolyte solution. • The ZnO coating can improve the electronic conductivity and lithium ion diffusion coefficient, which contributes to a great improvement in cyclic and high rate capabilities of LTO electrode. • The ZnO coating on LTO may be an effective method to solve the gassing behavior of LTO based battery and promote its wide application in lithium ion power battery. - Abstract: Li4Ti5O12 (LTO) based batteries have severe gassing behavior during charge/discharge and storage process. The interfacial reactions between LTO and electrolyte solution may be the main reason. In this work, the LTO spinel particles are modified with ZnO coating using a chemical process to reduce the surface reactivity of LTO particles. Results show that the ZnO coating can effectively stabilize the electrode/electrolyte interface and suppress the formation of a solid electrolyte interface (SEI) film. Simultaneously, this ZnO modification can improve the electronic conductivity and lithium ion diffusion coefficient, which contributes to a great improvement in cyclic and high rate capabilities of

  10. Hydrogen evolution reaction at Ru-modified nickel-coated carbon fibre in 0.1 M NaOH

    Directory of Open Access Journals (Sweden)

    Pierożyński Bogusław

    2015-03-01

    Full Text Available The electrochemical activity towards hydrogen evolution reaction (HER was studied on commercially available (Toho-Tenax and Ru-modified nickel-coated carbon fibre (NiCCF materials. Quality and extent of Ru electrodeposition on NiCCF tows were examined by means of scanning electron microscopy (SEM. Kinetics of the hydrogen evolution reaction were investigated at room temperature, as well as over the temperature range: 20-50°C in 0.1 M NaOH solution for the cathodic overpotential range: -100 to -300 mV vs. RHE. Corresponding values of charge-transfer resistance, exchange current-density for the HER and other electrochemical parameters for the examined fibre tow composites were recorded.

  11. Reaction Mechanisms for the Limited Reversibility of Li-O2 Chemistry in Organic Carbonate Electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Wu; Xu, Kang; Viswanathan, Vilayanur V.; Towne, Silas A.; Hardy, John S.; Xiao, Jie; Nie, Zimin; Hu, Dehong; Wang, Deyu; Zhang, Jiguang

    2011-11-15

    The Li-O2 chemistry in nonaqueous carbonate electrolytes and the underneath reason of its limited reversibility was exhaustively investigated. The discharge products collected from the air cathode in a Li-O2 battery at different depth of discharge (DOD) were systematically analyzed with X-ray diffraction. It is revealed that, independent of the discharge depth, lithium alkylcarbonate (either lithium propylenedicarbonate - LPDC, or lithium ethylenedicarbonate - LEDC, with other related derivatives) and lithium carbonate (Li2CO3) are always the main products, obviously originated from the electrolyte solvents propylene carbonate (PC) and ethylene carbonate (EC). These lithium alkylcarbonates are obviously generated from the single-electron reductive decomposition of the corresponding carbonate solvents initiated by the attack of superoxide radical anions. On the other hand, neither lithium peroxide (Li2O2) nor lithium oxide (Li2O) is detected. More significantly, from in situ gas chromatography/mass spectroscopy it is found that Li2CO3 and Li2O cannot be oxidized even when charged up to 4.6 V vs. Li/Li+, while LPDC, LEDC and Li2O2 are readily able to, with CO2 and CO released with the re-oxidation of LPDC and LEDC. It is therefore concluded that the quasi-reversibility of Li-O2 chemistry observed hitherto in an organic carbonate-based electrolyte is actually reliant on the formation of lithium alkylcarbonates through the reductive decomposition of carbonate solvents during discharge process and the subsequent oxidation of these same alkylcarbonates during charge process. It is the poor oxidizability of these alkylcarbonate species that constitutes the obstruction to an ideal rechargeable Li-O2 battery.

  12. A prediction model for concrete carbonation based on coupled CO²-H²O-ions transfers and chemical reactions

    OpenAIRE

    Thiery, M.; DANGLA, P; Villain, G.; Platret, G.

    2005-01-01

    It is a recognized fact that steel corrosion reduces the serviceability and safety performance of reinforced concrete. Usually high alkaline conditions in concrete lead to the formation of a passive layer at the steel surface. However the natural diffusion of the atmospheric carbon dioxide (CO²) into the concrete induces a decrease of the pore water pH value after reactions with hydrates such as portlandite Ca(OH)² and calcium silicate hydrates C-S-H. Under low-pH conditions, the passive laye...

  13. Synthesis and Characterization of Graphene and Graphene Oxide Based Palladium Nanocomposites and Their Catalytic Applications in Carbon-Carbon Cross-Coupling Reactions

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Minjae [Kunsan National Univ., Gunsan (Korea, Republic of); Kim, Bohyun; Lee, Yuna; Kim, Beomtae; Park, Joon B. [Chonbuk National Univ., Jeonju (Korea, Republic of)

    2014-07-15

    We have developed an efficient method to generate highly active Pd and PdO nanoparticles (NPs) dispersed on graphene and graphene oxide (GO) by an impregnation method combined with thermal treatments in H{sub 2} and O{sub 2} gas flows, respectively. The Pd NPs supported on graphene (Pd/G) and the PdO NPs supported on GO (PdO/GO) demonstrated excellent carbon-carbon cross-coupling reactions under a solvent-free, environmentally-friendly condition. The morphological and chemical structures of PdO/GO and Pd/G were fully characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). We found that the remarkable reactivity of the Pd/G and PdO/GO catalysts toward the cross-coupling reaction is attributed to the high degree of dispersion of the Pd and PdO NPs while the oxidative states of Pd and the oxygen functionalities of graphene oxide are not critical for their catalytic performance.

  14. A DFT study on the mechanism of palladium-catalyzed divergent reactions of 1,6-enyne carbonates

    Indian Academy of Sciences (India)

    Xing Hui Zhang; Zhi Yuan Geng; Teng Niu; Ke Tai Wang

    2015-03-01

    The reaction mechanisms of palladium-catalyzed divergent reactions of 1,6-enyne carbonates have been investigated using DFT calculations at the B3LYP/6-31G(d,p) (LanL2DZ for Pd) level. Solvent effects on these reactions have been considered by the polarizable continuum model (PCM) for the solvent (DMF). The formation of vinylidenepyridines and vinylidenepyrrolidines were generated through 5-exo-dig cyclization or 6-endo-dig cyclization. Our calculation results suggested the following: (i) The first step of the whole cycle is the rate-determining step, which causes allenic palladium intermediate through two plausible pathways. This intermediate provides the corresponding products and releases the palladium catalyst by a subsequent hydrogen transfer and elimination process. (ii) For the catalyst CH3OPdH, the reaction could occur through two possible pathways, but 5-exo-dig cyclization is favoured over 6-endo-dig cyclization. However, when the hydrogen atom is substituted with a phenyl group, the energy barriers for 5-exo-dig cyclization or 6-endo-dig cyclization become relatively high, 18.0–28.5 kcal/mol. The computational results provide good explanation for the experimental observations.

  15. In Situ Evaluation of Water-Rock Reactions during Carbon Dioxide Injection in Basaltic and Metasedimentary Rocks

    Science.gov (United States)

    Matter, J. M.; Assayag, N.; Goldberg, D.; Takahashi, T.

    2006-12-01

    Large differences between laboratory and field derived mineral reaction rates underscore the importance of evaluating mineral-fluid reactions under in situ conditions in a natural environment. This study investigates the extent of in situ water-rock reactions in basaltic and metasedimentary rocks (rich in Ca, Mg silicates) after the injection of CO2 enriched water, with the objective of providing information pertinent to permanent storage of anthropogenic CO2 in geologic reservoirs. CO2 injections were conducted using a single-well push-pull testing strategy. CO2 saturated water (pH 3.5) was injected into a hydraulically isolated and permeable aquifer in a 300-m experimental borehole. Water samples were retrieved after the CO2 injection. Mass transfer terms for Ca, Mg, Na, and Si were determined by using the measured ion concentrations. Using the mass balance, the weeks-long incubation time of the injected solution, and geometric estimates of the reactive surface area of the host rocks, in situ bulk rock dissolution rates of aquifer material were estimated. In addition, δ13C data coupled with total CO2 concentration were used as a tracer to quantitatively evaluate processes such as carbonate dissolution and precipitation, oxidation of organic matter and biological activity within the aquifer. Results show that the injected CO2 was neutralized within several days by two processes; mixing with aquifer water, and rock-water reactions. Calculated bulk rock dissolution rates decrease with increasing pH. The pH dependence of the dissolution rate for Ca is twice as large as for Mg, strongly favoring Ca release and possibly suggesting an additional source of Ca besides silicate minerals. Analyses of δ13C on water and rock samples confirm dissolution of calcium carbonates within the aquifer.

  16. Electrocatalytic studies of osmium-ruthenium carbonyl cluster compounds for their application as methanol-tolerant cathodes for oxygen reduction reaction and carbon monoxide-tolerant anodes for hydrogen oxidation reaction

    Energy Technology Data Exchange (ETDEWEB)

    Borja-Arco, E.; Uribe-Godinez, J.; Castellanos, R.H. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, Escobedo (Mexico); Altamirano-Gutierrez, A.; Jimenez-Sandoval, O. [Centro de Investigacion y de Estudios Avanzados del Inst. Politecnico Nacional, Querataro (Mexico)

    2006-07-01

    This paper provided details of an electrokinetic study of novel electrocatalytic materials capable of performing both the oxygen reduction reaction (ORR) and the hydrogen oxidation reaction (HOR). Osmium-ruthenium carbonyl cluster compounds (Os{sub x}Ru{sub 3}(CO){sub n}) were synthesized by chemical condensation in non-polar organic solvents at different boiling points and refluxing temperatures. Three different non-polar organic solvents were used: (1) n-nonane; o-xylene; and 1,2-dichlorobenzene. The electrocatalysts were characterized by Fourier Transform Infra-red (FTIR) spectroscopy, scanning electron microscopy (SEM) and X-ray diffraction (XRD). A rotating disk electrode technique was used to analyze the materials. Results of the analysis showed that the materials performed ORR in both the presence and absence of carbon monoxide (CO), and that electrocatalysts were not poisoned by the presence of CO. Cyclic voltamperometry for the disk electrodes showed that the electrochemical behaviour of the compounds in the acid electrolyte was similar in the presence or absence of methanol. The Tafel slope, exchange current density and the transfer coefficient were also investigated. The electrokinetic parameters for the ORR indicated that the materials with the highest electrocatalytic activity were synthesized in 1,2-dichlorobenzene. Electrocatalytic activity during HOR were prepared in n-nonane. It was concluded that the new materials are good candidates for use as both a cathode and an anode in proton exchange membrane fuel cells (PEMFCs) and direct methanol fuel cells (DMFCs). 7 refs., 2 tabs., 7 figs.

  17. Non-Enzymatic-Browning-Reaction: A Versatile Route for Production of Nitrogen-Doped Carbon Dots with Tunable Multicolor Luminescent Display

    OpenAIRE

    Weili Wei; Can Xu; Li Wu; Jiasi Wang; Jinsong Ren; Xiaogang Qu

    2014-01-01

    The non-enzymatic browning, namely Maillard reaction is commonly invoked to account for abiotic chemical transformations of organic matter. Here we report a new reaction pathway via the Maillard reaction to systematically synthesize a series of nitrogen-doped carbon dots (C-dots) with superhigh quantum yield (QY) and tunable multicolor luminescent displayment. The starting materials are glucose and the serial amino acid analogues which allow systemically controlling luminescent and physicoche...

  18. Electrochemical activity and durability of platinum nanoparticles supported on ordered mesoporous carbons for oxygen reduction reaction

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Shou-Heng [Institute of Atomic and Molecular Sciences, Academia Sinica, P.O. Box 23-166, Taipei 10617 (China); Chiang, Chien-Chang; Wu, Min-Tsung; Liu, Shang-Bin [Institute of Atomic and Molecular Sciences, Academia Sinica, P.O. Box 23-166, Taipei 10617 (China); Department of Chemistry, National Taiwan Normal University, Taipei 11677 (China)

    2010-08-15

    A facile procedure for synthesizing platinum nanoparticles (NPs) studded in ordered mesoporous carbons (Pt-OMCs) based on the organic-organic self-assembly (one-pot) approach is reported. These Pt-OMCs, which can be easily fabricated with controllable Pt loading, were found to possess high surface areas, highly accessible and stable active sites and superior electrocatalytic properties pertinent as cathode catalysts for hydrogen-oxygen fuel cells. The enhanced catalytic activity and durability observed for the Pt-OMC electrocatalysts are attributed to the strengthened interactions between the Pt catalyst and the mesoporous carbon that effectively precludes migration and/or agglomeration of Pt NPs on the carbon support. (author)

  19. A nitrogen-doped mesoporous carbon containing an embedded network of carbon nanotubes as a highly efficient catalyst for the oxygen reduction reaction.

    Science.gov (United States)

    Li, Jin-Cheng; Zhao, Shi-Yong; Hou, Peng-Xiang; Fang, Ruo-Pian; Liu, Chang; Liang, Ji; Luan, Jian; Shan, Xu-Yi; Cheng, Hui-Ming

    2015-12-01

    A nitrogen-doped mesoporous carbon containing a network of carbon nanotubes (CNTs) was produced for use as a catalyst for the oxygen reduction reaction (ORR). SiO2 nanoparticles were decorated with clusters of Fe atoms to act as catalyst seeds for CNT growth, after which the material was impregnated with aniline. After polymerization of the aniline, the material was pyrolysed and the SiO2 was removed by acid treatment. The resulting carbon-based hybrid also contained some Fe from the CNT growth catalyst and was doped with N from the aniline. The Fe-N species act as active catalytic sites and the CNT network enables efficient electron transport in the material. Mesopores left by the removal of the SiO2 template provide short transport pathways and easy access to ions. As a result, the catalyst showed not only excellent ORR activity, with 59 mV more positive onset potential and 30 mV more positive half-wave potential than a Pt/C catalyst, but also much longer durability and stronger tolerance to methanol crossover than a Pt/C catalyst.

  20. Effects of reaction conditions on hydrogen production and carbon nanofiber properties generated by methane decomposition in a fixed bed reactor using a NiCuAl catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Suelves, I.; Pinilla, J.L.; Lazaro, M.J.; Moliner, R. [Instituto de Carboquimica CSIC, Miguel Luesma Castan, 4, 50015 Zaragoza (Spain); Palacios, J.M. [Instituto de Catalisis y Petroleoquimica, CSIC, Cantoblanco, Marie Curie 2, 28049 Madrid (Spain)

    2009-07-01

    In this paper, the results obtained in the catalytic decomposition of methane in a fixed bed reactor using a NiCuAl catalyst prepared by the fusion method are presented. The influences of reaction temperature and space velocity on hydrogen concentration in the outlet gases, as well as on the properties of the carbon produced, have been investigated. Reaction temperature and the space velocity both increase the reaction rate of methane decomposition, but also cause an increase in the rate of catalyst deactivation. Under the operating conditions used, the carbon product is mainly deposited as nanofibers with textural properties highly correlated with the degree of crystallinity. (author)

  1. Hypernuclear production cross section in the reaction of 6Li + 12C at 2A GeV

    Directory of Open Access Journals (Sweden)

    C. Rappold

    2015-07-01

    Full Text Available Hypernuclear production cross sections have been deduced for the first time with induced reaction of heavy ion beam on fixed target and by means of the invariant mass method by the HypHI Collaboration exploiting the reaction of 6Li + 12C at 2A GeV or sNN=2.70 GeV. A production cross section of 3.9±1.4 μb for 3ΛH and of 3.1±1.0 μb for 4ΛH respectively in the projectile rapidity region was inferred as well as the total production cross section of the Λ hyperon was measured and found to be equal to 1.7±0.8 mb. A global fit based on a Bayesian approach was performed in order to include and propagate statistical and systematic uncertainties. Production ratios of 3ΛH/4ΛH, 3ΛH/Λ and 4ΛH/Λ were included in the inference procedure. The strangeness population factors S3 and S4 of 3ΛH and 4ΛH respectively were extracted. In addition, the multiplicities of the Λ hyperon, 3ΛH, and 4ΛH together with the rapidity and transversal momentum density distributions of the observed hypernuclei were extracted and reported.

  2. Study of the Particle Production in $^{12}$C Induced Heavy Ion Reactions at 86 MeV/N

    CERN Multimedia

    2002-01-01

    The aim of this experiment is to study various characteristics of light and heavy particle production in |1|2C induced reactions if possible over the whole unexplored energy region 50-86~MeV/N. In particular we want to investigate how the correlations in the multiparticle events can help us to distinguish bet existing models. \\\\ \\\\ Two-proton large-angle correlations and correlations between two heavier (Z~=~1 or 2) particles are studied with scintillator +~NaI and range telescopes, complemented with a 24 telescope scintillator wall for projectile fragments. Thereby we receive information about the reaction plane and the impact parameter in coincidence with the two-particle correlation spectra. Small @Dp correlations can also be studied. The inclusive @p|+ and @p|- production has been followed far below the nucleon-nucleon threshold. Pions are thereby identified from @DE-E correlations and the @p|+ decay in plastic range telescopes. These results are now followed up by @p-projectile fragment and @p-p correlat...

  3. Absolute hydrogen depth profiling using the resonant $^{1}$H($^{15}$N,$\\alpha\\gamma$)$^{12}$C nuclear reaction

    CERN Document Server

    Reinhardt, Tobias P; Bemmerer, Daniel; Stöckel, Klaus; Wagner, Louis

    2016-01-01

    Resonant nuclear reactions are a powerful tool for the determination of the amount and profile of hydrogen in thin layers of material. Usually, this tool requires the use of a standard of well-known composition. The present work, by contrast, deals with standard-less hydrogen depth profiling. This approach requires precise nuclear data, e.g. on the widely used $^{1}$H($^{15}$N,$\\alpha\\gamma$)$^{12}$C reaction, resonant at 6.4\\,MeV $^{15}$N beam energy. Here, the strongly anisotropic angular distribution of the emitted $\\gamma$-rays from this resonance has been re-measured, resolving a previous discrepancy. Coefficients of (0.38$\\pm$0.04) and (0.80$\\pm$0.04) have been deduced for the second and fourth order Legendre polynomials, respectively. In addition, the resonance strength has been re-evaluated to (25.0$\\pm$1.5)\\,eV, 10\\% higher than previously reported. A simple working formula for the hydrogen concentration is given for cases with known $\\gamma$-ray detection efficiency. Finally, the absolute approach i...

  4. Absolute hydrogen depth profiling using the resonant 1H(15N, αγ)12C nuclear reaction

    Science.gov (United States)

    Reinhardt, Tobias P.; Akhmadaliev, Shavkat; Bemmerer, Daniel; Stöckel, Klaus; Wagner, Louis

    2016-08-01

    Resonant nuclear reactions are a powerful tool for the determination of the amount and profile of hydrogen in thin layers of material. Usually, this tool requires the use of a standard of well-known composition. The present work, by contrast, deals with standard-less hydrogen depth profiling. This approach requires precise nuclear data, e.g. on the widely used 1 H(15 N, αγ)12 C reaction, resonant at 6.4 MeV 15 N beam energy. Here, the strongly anisotropic angular distribution of the emitted γ -rays from this resonance has been re-measured, resolving a previous discrepancy. Coefficients of (0.38 ± 0.04) and (0.80 ± 0.04) have been deduced for the second and fourth order Legendre polynomials, respectively. In addition, the resonance strength has been re-evaluated to (25.0 ± 1.5) eV, 10% higher than previously reported. A simple working formula for the hydrogen concentration is given for cases with known γ -ray detection efficiency. Finally, the absolute approach is illustrated using two examples.

  5. Supercritical carbon dioxide as an innovative reaction medium for selective oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Loeker, F.; Leitner, W. [Max-Planck-Institut fuer Kohlenforschung, Muelheim an der Ruhr (Germany)

    1998-12-31

    Although the catalytic efficiency of all catalytic oxidation processes studied in scCO{sub 2} up to now is far from being satisfactory, the principle possibility to carry out such reactions in this medium is clearly evident. Future research in our group will be directed towards the development of homogeneous and heterogeneous catalysts that are adopted to the special requirements of both the oxidation process and the supercritical reaction medium. Preliminary results from these studies regarding the epoxidation of olefins with molecular oxygen as oxidant will be presented on the conference poster. (orig.)

  6. Study of Target Fragmentation in the Interaction of 86 MeV/A $^{12}$Carbon with Tantalum, Bismuth and Uranium

    CERN Multimedia

    2002-01-01

    Using radiochemical techniques we will ; a)~~measure the target fragment mass and charge distributions from the interaction of 86~MeV/A |1|2C with Ta, Bi and U; ; b)~~measure the target fragment forward momentum and average kinetic energy using the thick target-thick catcher technique for the above reactions; and ; c)~~measure the target fragment angular and differential energy distributions using thin target-thin catcher techniques for the reactions with Ta and U. \\\\ \\\\ These measurements should allow us to better characterize the transition between low energy and realistic heavy ion reaction mechanisms.

  7. Electrophysiological Monitoring in Patients With Tumors of the Skull Base Treated by Carbon-12 Radiation Therapy

    Energy Technology Data Exchange (ETDEWEB)

    Carozzo, Simone [Department of Neuroscience, Ophthalmology, and Genetics, University of Genova, Genova (Italy); Schardt, Dieter [Department of Biophysics, GSI Helmholtzzentrum für Schwerionenforschung, Darmstadt (Germany); Narici, Livio [Department of Physics, University of Rome Tor Vergata, Rome (Italy); Combs, Stephanie E.; Debus, Jürgen [Department of Radiation Oncology, University of Heidelberg, Heidelberg (Germany); Sannita, Walter G., E-mail: wgs@dism.unige.it [Department of Neuroscience, Ophthalmology, and Genetics, University of Genova, Genova (Italy); Department of Psychiatry, State University of New York, Stony Brook, New York (United States)

    2013-03-15

    Purpose: To report the results of short-term electrophysiologic monitoring of patients undergoing {sup 12}C therapy for the treatment of skull chordomas and chondrosarcomas unsuitable for radical surgery. Methods and Materials: Conventional electroencephalogram (EEG) and retinal and cortical electrophysiologic responses to contrast stimuli were recorded from 30 patients undergoing carbon ion radiation therapy, within a few hours before the first treatment and after completion of therapy. Methodologies and procedures were compliant with the guidelines of the International Federation for Clinical Neurophysiology and International Society for Clinical Electrophysiology of Vision. Results: At baseline, clinical signs were reported in 56.6% of subjects. Electrophysiologic test results were abnormal in 76.7% (EEG), 78.6% (cortical evoked potentials), and 92.8% (electroretinogram) of cases, without correlation with neurologic signs, tumor location, or therapy plan. Results on EEG, but not electroretinograms and cortical responses, were more often abnormal in patients with reported clinical signs. Abnormal EEG results and retinal/cortical responses improved after therapy in 40% (EEG), 62.5% (cortical potentials), and 70% (electroretinogram) of cases. Results on EEG worsened after therapy in one-third of patients whose recordings were normal at baseline. Conclusions: The percentages of subjects whose EEG results improved or worsened after therapy and the improvement of retinal/cortical responses in the majority of patients are indicative of a limited or negligible (and possibly transient) acute central nervous system toxicity of carbon ion therapy, with a significant beneficial effect on the visual pathways. Research on large samples would validate electrophysiologic procedures as a possible independent test for central nervous system toxicity and allow investigation of the correlation with clinical signs; repeated testing over time after therapy would demonstrate, and may

  8. Iron encapsulated within pod-like carbon nanotubes for oxygen reduction reaction.

    Science.gov (United States)

    Deng, Dehui; Yu, Liang; Chen, Xiaoqi; Wang, Guoxiong; Jin, Li; Pan, Xiulian; Deng, Jiao; Sun, Gongquan; Bao, Xinhe

    2013-01-01

    Chainmail for catalysts: a catalyst with iron nanoparticles confined inside pea-pod-like carbon nanotubes exhibits a high activity and remarkable stability as a cathode catalyst in polymer electrolyte membrane fuel cells (PEMFC), even in presence of SO(2). The approach offers a new route to electro- and heterogeneous catalysts for harsh conditions.

  9. Kinetic and mechanistic studies on the reaction of the vitamin B12 complex aquacobalamin with the HNO donor Angeli's salt: Angeli's salt and HNO react with aquacobalamin.

    Science.gov (United States)

    Subedi, Harishchandra; Hassanin, Hanaa A; Brasch, Nicola E

    2014-02-01

    We report the first studies on the reaction between an HNO donor compound and vitamin B12 complexes. Kinetic and mechanistic studies have been carried out on the reaction between the vitamin B12 derivative aquacobalamin (H2OCbl(+)/HOCbl; pKa = 7.8) and the HNO donor Angeli's salt. Studies were carried out with aquacobalamin in excess, since nitrite also reacts with aquacobalamin to form nitrocobalamin (NO2Cbl). At pH 10.80 the reaction instead switches predominantly to a mechanism in which spontaneous decomposition of Angeli's salt to give HNO and nitrite becomes the rate-determining step, followed by the rapid reaction between aquacobalamin and HNO/NO(-) to again give NOCbl. Both reactions proceed with a 1:1 stoichiometry and formation of nitrite is confirmed using the Griess assay. PMID:24437629

  10. Nitrogen and Sulfur Co-doped Mesoporous Carbon Materials as Highly Efficient Electrocatalysts for Oxygen Reduction Reaction

    International Nuclear Information System (INIS)

    Nitrogen and sulfur co-doped mesoporous carbon materials are synthesized by pyrolyzing FeSO4 + poly(ethyleneimine) + template SiO2 mixture at a high temperature without additional dopant precursors. For post-treatment, acid leaching is used to remove the metal, and the heat-treatment is tailored to optimize the catalytic activity of the catalysts toward the oxygen reduction reaction (ORR) in acidic solution. Scanning electron microscopy, X-ray diffraction, low-temperature N2 adsorption, X-ray photoelectron spectroscopy and inductively coupled plasma are used to characterize the catalysts' morphologies, structures, and compositions. Rotating disk electrode and rotating ring-disk electrode techniques are employed to quantitatively obtain the ORR kinetic constants and determine the reaction mechanisms. The ORR activity is highly improved by reheating the catalyst after H2SO4 leaching with improved half-wave potential of 0.68 V vs. RHE, and ORR electron number larger than 3.76. Moreover, increasing the catalyst loading of 800 μg cm−2 exhibits only ∼36 mV deviation from Pt/C. It is believed that the synergetic effect between the Fe-, N- and S-containing active sites and the modified carbon matrix structure due to H2SO4 leaching and reheating should make contribution to the high ORR activity

  11. Experimental study of bound states in 12Be through low-energy 11Be(d,p)-transfer reactions

    DEFF Research Database (Denmark)

    Johansen, Jacob S.; Bildstein, V.; Borge, M. J. G.;

    2013-01-01

    The bound states of 12Be have been studied through a 11Be(d,p)12Be transfer reaction experiment in inverse kinematics. A 2.8 MeV/u beam of 11Be was produced using the REX-ISOLDE facility at CERN. The outgoing protons were detected with the T-REX silicon detector array. The MINIBALL germanium arra...

  12. The Development and Application of Two-Chamber Reactors and Carbon Monoxide Precursors for Safe Carbonylation Reactions.

    Science.gov (United States)

    Friis, Stig D; Lindhardt, Anders T; Skrydstrup, Troels

    2016-04-19

    Low molecular weight gases (e.g., carbon monoxide, hydrogen, and ethylene) represent vital building blocks for the construction of a wide array of organic molecules. Whereas experimental organic chemists routinely handle solid and liquid reagents, the same is not the case for gaseous reagents. Synthetic transformations employing such reagents are commonly conducted under pressure in autoclaves or under atmospheric pressure with a balloon setup, which necessitates either specialized equipment or potentially hazardous and nonrecommended installations. Other safety concerns associated with gaseous reagents may include their toxicity and flammability and, with certain gases, their inability to be detected by human senses. Despite these significant drawbacks, industrial processes apply gaseous building blocks regularly due to their low cost and ready availability but nevertheless under a strictly controlled manner. Carbon monoxide (CO) fits with all the parameters for being a gas of immense industrial importance but with severe handling restrictions due to its inherent toxicity and flammability. In academia, as well as research and development laboratories, CO is often avoided because of these safety issues, which is a limitation for the development of new carbonylation reactions. With our desire to address the handling of CO in a laboratory setting, we designed and developed a two-chamber reactor (COware) for the controlled delivery and utilization of stoichiometric amounts of CO for Pd-catalyzed carbonylation reactions. In addition to COware, two stable and solid CO-releasing molecules (COgen and SilaCOgen) were developed, both of which release CO upon activation by either Pd catalysis or fluoride addition, respectively. The unique combination of COware with either COgen or SilaCOgen provides a simple reactor setup enabling synthetic chemists to easily perform safe carbonylation chemistry without the need for directly handling the gaseous reagent. With this technology

  13. Synthesis and reaction of 16-electron CptRh halfsandwich complexes containing 1,2-dichalcogenolate carborane ligands

    Institute of Scientific and Technical Information of China (English)

    KONG Qingan; JIN Guoxin; CAI Shuyi; WENG Linhong

    2003-01-01

    The reactions of [CptRhCl((-Cl)]2 (1) (Cpt = tBu2C5H3) with Li2E2C2B10H10 (E = S, Se) lead to the green 16-electron dichalcogenolate complexes CptRh(E2C2B10H10) [E = S(2a), Se(2b)]. The 16-electron complexes 2a and 2b can take up two-electron donor ligands such as tert-butyl isonitrile and carbon monoxide to give the 18-electron dichalcogenolate derivatives Cpt(L)(E2C2B10H10) [L = tBuNC, E = S(3a), Se(3b); L = CO, E = S(4a), Se(4b)]. The molecular structures of complexes 2a and 3a were determined by X-ray crystal structure analysis. The molecular structure of 16- electron complex 2a shows the pseudoaromatic system in IrSe2C2 five numbered ring.

  14. Modular, Catalytic Enantioselective Construction of Quaternary Carbon Stereocenters by Sequential Cross-Coupling Reactions.

    Science.gov (United States)

    Potter, Bowman; Edelstein, Emma K; Morken, James P

    2016-07-01

    The catalytic Suzuki-Miyaura cross-coupling with chiral γ,γ-disubstituted allylboronates in the presence of RuPhos ligand occurs with high regioselectivity and enantiospecificity, furnishing nonracemic compounds with quaternary centers. Mechanistic experiments suggest that the reaction occurs by transmetalation with allyl migration, followed by rapid reductive elimination.

  15. Sustainable Ways of Combining Reactions and Separations Using Ionic Liquids and Carbon Dioxide

    NARCIS (Netherlands)

    Kazemi, S.

    2013-01-01

    Traditional chemical processes show shortcomings caused by using volatile organic compounds as solvents during reactions and separations. Therefore, it is necessary to address this issue by moving toward more environmentally friendly processes. This is possible by using less toxic and hazardous solv

  16. Enhancement of delayed hypersensitivity inflammatory reactions in guinea pig skin by 12(R)-hydroxy-5,8,14-eicosatrienoic acid.

    Science.gov (United States)

    Conners, M S; Schwartzman, M L; Quan, X; Heilman, E; Chauhan, K; Falck, J R; Godfrey, H P

    1995-01-01

    Delayed-type hypersensitivity (DTH) reactions are initiated by sensitized T cells. Their progression is dependent upon the local release of various autacoids, including cytokines and eicosanoids, by T cells, infiltrating inflammatory cells, and resident tissue cells. 12(R)-hydroxy-5,8,14-eicosatrienoic acid [12(R)-HETrE], an eicosanoid produced by skin and cornea, possesses potent proinflammatory properties at picomolar concentrations including vasodilation, increase in membrane permeability, neutrophil chemotaxis, and angiogenesis. Because DTH reactions are associated with many of these same phenomena, we examined the effect of 12(R)-HETrE and related 12-hydroxyeicosanoids on the expression of DTH to purified protein derivative of tuberculin in sensitized guinea pigs. In the absence of purified protein derivative of tuberculin, none of the eicosanoids evoked erythema or edema after intradermal injection at doses up to 100 pmol. When injected together with purified protein derivative of tuberculin, 12(R)-hydroxy-5,8,10,14-eicosatetraenoic acid [12(R)-HETE], but not its enantiomer 12(S)-HETE, significantly inhibited macroscopic expression of delayed reactivity (erythema) only at the highest dose tested, 10 pmol. In contrast, 12(R)-HETrE significantly enhanced expression of DTH at doses between 1 fmol and 1 pmol (50% and 30% increases above control, respectively). Its stereoisomer, 12(S)-HETrE, did not enhance DTH at any tested dose, but was able to block the activity of 12(R)-HETrE when injected simultaneously. Enhancement or inhibition of visible skin responses was not associated with qualitative or quantitative changes in cellular infiltrates at the reaction site. 12(R)-HETrE had no effect on the nonimmunologic inflammatory skin reaction induced by phorbol myristate acetate, suggesting selectivity toward DTH. We conclude that 12(R)-HETrE enhances DTH via a yet to be determined mechanism and that its stereoisomer, 12(S)-HETrE, may be a useful antagonist for

  17. Measurement of the 12C(e,e′p)11B two-body breakup reaction at high missing momentum

    International Nuclear Information System (INIS)

    The five-fold differential cross section for the 12C(e,e′p)11B reaction was determined over a missing momentum range of 200–400 MeV c−1, in a kinematics regime with xB>1 and Q2=2.0 (GeV c−1)2. A comparison of the results with previous lower missing momentum data and with theoretical models are presented. The extracted distorted momentum distribution is shown to be consistent with previous data and extends the range of available data up to 400 MeV c−1. The theoretical calculations are from two very different approaches, one mean field and the other short range correlated; yet for this system the two approaches show striking agreement with the data and each other up to a missing momentum value of 325 MeV c−1. For larger momenta, the calculations diverge which is likely due to the factorization approximation used in the short range approach. (paper)

  18. Light charged-particle production in 96 MeV neutron-induced reactions on carbon and oxygen

    International Nuclear Information System (INIS)

    In recent years, an increasing number of applications involving fast neutrons have been developed or are under consideration, e.g. radiation treatment of cancer, neutron dosimetry at commercial aircraft altitudes, soft-error effects in computer memories, accelerator-driven transmutation of nuclear waste and energy production and determination of the response of neutron detectors. Data on light-ion production in light nuclei such as carbon, nitrogen and oxygen are particularly important in calculations of dose distributions in human tissue for radiation therapy at neutron beams, and for dosimetry of high-energy neutrons produced by high-energy cosmic radiation interacting with nuclei (nitrogen and oxygen) in the atmosphere. When studying neutron dose effects, it is especially important to consider carbon and oxygen, since they are, by weight, the most abundant elements in human tissue. Preliminary experimental double-differential cross sections of inclusive light-ion (p, d, t, 3He and α) production in carbon induced by 96-MeV neutrons have been presented. Energy spectra were measured at eight laboratory angles: 20, 40, 60, 80, 100, 120, 140 and 160 deg.. Measurements were performed at The Svedberg Laboratory (TSL), Uppsala, using the dedicated MEDLEY experimental setup. The authors have earlier reported experimental double-differential cross sections of inclusive light-ion production in oxygen. In this paper, the deduced kerma coefficients for oxygen has been presented and compared with reaction model calculations. (authors)

  19. Enhanced catalysis of the electrochemical hydrogen evolution reaction using composites of molybdenum-based compounds, gold nanoparticles and carbon.

    Science.gov (United States)

    Joshi, Ubisha; Lee, Jing; Giordano, Cristina; Malkhandi, Souradip; Yeo, Boon Siang

    2016-08-21

    Molybdenum nitride has been recently reported to interact synergistically with gold to show an enhanced activity for the electrochemical hydrogen evolution reaction (2H(+) + 2e(-)→ H2, HER). In this work, we elucidated the roles of nitrogen, carbon, molybdenum and gold on this observed phenomenon. Composites of Mo-based compounds, carbon black (black pearl 2000) and/or Au nanoparticles (AuNP) were prepared, and their activities for the HER in a 0.5 M H2SO4 electrolyte were measured using linear sweep voltammetry. We show and discuss here for the first time that, while the presence of carbon is necessary for the synergy phenomenon, the nitrogen atoms present in the compounds play no apparent role in this synergy. In fact, all the compounds containing Mo, namely Mo2N, MoB and metallic Mo(0), exhibited extensive synergy with Au for the HER. A hypothesis for the enhanced catalysis of H2 evolution by the mixed metal composites is proposed and discussed. PMID:27424516

  20. Effect of reaction environments on the reactivity of PCB (2-chlorobiphenyl) over activated carbon impregnated with palladized iron

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Hyeok [Department of Civil Engineering, University of Texas at Arlington, 416 Yates Drive, Arlington, TX 76019-0308 (United States); Al-Abed, Souhail R., E-mail: al-abed.souhail@epa.gov [National Risk Management Research Laboratory, U.S. Environmental Protection Agency, 26 West Martin Luther King Drive, Cincinnati, OH 45268 (United States)

    2010-07-15

    Reactive activated carbon (RAC) impregnated with palladized iron nanoparticles has been developed to treat polychlorinated biphenyls (PCBs). In this study, we evaluated the effects of various reaction environments on the adsorption-mediated dechlorination of 2-chlorobiphenyl (2-ClBP) in the RAC system. The results were discussed in close connection to the implementation issue of the RAC system for the remediation of contaminated sites with PCBs. Adsorption event of 2-ClBP onto RAC limited the overall performance under condition with a 2-ClBP/RAC mass ratio of less than 1.0 x 10{sup -4} above which dechlorination of 2-ClBP adsorbed to RAC was the reaction rate-determining step. Acidic and basic conditions were harmful to 2-ClBP adsorption and iron stability while neutral pH showed the highest adsorption-promoted dechlorination of 2-ClBP and negligible metal leaching. Coexisting natural organic matter (NOM) slightly inhibited 2-ClBP adsorption onto RAC due to the partial partitioning of 2-ClBP into NOM in the liquid phase while the 2-ClBP absorbed into NOM, which also tended to adsorb onto RAC, was less available for the dechlorination reaction. Common anions slowed down 2-ClBP adsorption but adsorbed 2-ClBP was almost simultaneously dechlorinated. Some exceptions included strong inhibitory effect of carbonate species on 2-ClBP adsorption and severe detrimental effect of sulfite on 2-ClBP dechlorination. Results on treatment of 2-ClBP spiked to actual sediment supernatants implied site-specific reactivity of RAC.

  1. Preparation of carbon nitride fine powder by laser induced gas-phase reactions

    Science.gov (United States)

    Alexandrescu, R.; Huisken, F.; Pugna, G.; Crunteanu, A.; Petcu, S.; Cojocaru, S.; Cireasa, R.; Morjan, I.

    We present the possibility of carbon nitride fine powder synthesis by sensitized laser pyrolysis of acethylene/nitrous oxide/ammonia mixtures. The powders were analyzed using X-ray diffraction, X-ray photoelectron spectroscopy (XPS) and IR transmission measurements. It was found that nitrogen was incorporated in powders and that in the carbon-nitrogen phases formed, the presence of the triple bonded C≡N was not detected. The majority of X-ray diffraction data suggests the presence of a mixture of the predicted α- and β-C3N4 structure, with an α-C3N4-like form being prevalent. The powders were found to be slightly contaminated by SF6 sensitizer products. Our results suggest that by improving the experimental parameters this contamination might be reduced and that the laser pyrolysis method offers possibilities for production of CxNy materials, with controlled composition.

  2. Multiplex quantification of 12 European Union authorized genetically modified maize lines with droplet digital polymerase chain reaction.

    Science.gov (United States)

    Dobnik, David; Spilsberg, Bjørn; Bogožalec Košir, Alexandra; Holst-Jensen, Arne; Žel, Jana

    2015-08-18

    Presence of genetically modified organisms (GMO) in food and feed products is regulated in many countries. The European Union (EU) has implemented a threshold for labeling of products containing more than 0.9% of authorized GMOs per ingredient. As the number of GMOs has increased over time, standard-curve based simplex quantitative polymerase chain reaction (qPCR) analyses are no longer sufficiently cost-effective, despite widespread use of initial PCR based screenings. Newly developed GMO detection methods, also multiplex methods, are mostly focused on screening and detection but not quantification. On the basis of droplet digital PCR (ddPCR) technology, multiplex assays for quantification of all 12 EU authorized GM maize lines (per April first 2015) were developed. Because of high sequence similarity of some of the 12 GM targets, two separate multiplex assays were needed. In both assays (4-plex and 10-plex), the transgenes were labeled with one fluorescence reporter and the endogene with another (GMO concentration = transgene/endogene ratio). It was shown that both multiplex assays produce specific results and that performance parameters such as limit of quantification, repeatability, and trueness comply with international recommendations for GMO quantification methods. Moreover, for samples containing GMOs, the throughput and cost-effectiveness is significantly improved compared to qPCR. Thus, it was concluded that the multiplex ddPCR assays could be applied for routine quantification of 12 EU authorized GM maize lines. In case of new authorizations, the events can easily be added to the existing multiplex assays. The presented principle of quantitative multiplexing can be applied to any other domain.

  3. Multiplex quantification of 12 European Union authorized genetically modified maize lines with droplet digital polymerase chain reaction.

    Science.gov (United States)

    Dobnik, David; Spilsberg, Bjørn; Bogožalec Košir, Alexandra; Holst-Jensen, Arne; Žel, Jana

    2015-08-18

    Presence of genetically modified organisms (GMO) in food and feed products is regulated in many countries. The European Union (EU) has implemented a threshold for labeling of products containing more than 0.9% of authorized GMOs per ingredient. As the number of GMOs has increased over time, standard-curve based simplex quantitative polymerase chain reaction (qPCR) analyses are no longer sufficiently cost-effective, despite widespread use of initial PCR based screenings. Newly developed GMO detection methods, also multiplex methods, are mostly focused on screening and detection but not quantification. On the basis of droplet digital PCR (ddPCR) technology, multiplex assays for quantification of all 12 EU authorized GM maize lines (per April first 2015) were developed. Because of high sequence similarity of some of the 12 GM targets, two separate multiplex assays were needed. In both assays (4-plex and 10-plex), the transgenes were labeled with one fluorescence reporter and the endogene with another (GMO concentration = transgene/endogene ratio). It was shown that both multiplex assays produce specific results and that performance parameters such as limit of quantification, repeatability, and trueness comply with international recommendations for GMO quantification methods. Moreover, for samples containing GMOs, the throughput and cost-effectiveness is significantly improved compared to qPCR. Thus, it was concluded that the multiplex ddPCR assays could be applied for routine quantification of 12 EU authorized GM maize lines. In case of new authorizations, the events can easily be added to the existing multiplex assays. The presented principle of quantitative multiplexing can be applied to any other domain. PMID:26169291

  4. Structural Basis on the Catalytic Reaction Mechanism of Novel 1,2-Alpha L-Fucosidase (AFCA) From Bifidobacterium Bifidum

    Energy Technology Data Exchange (ETDEWEB)

    Nagae, M.; Tsuchiya, A.; Katayama, T.; Yamamoto, K.; Wakatsuki, S.; Kato, R.

    2009-06-03

    1,2-alpha-L-fucosidase (AfcA), which hydrolyzes the glycosidic linkage of Fucalpha1-2Gal via an inverting mechanism, was recently isolated from Bifidobacterium bifidum and classified as the first member of the novel glycoside hydrolase family 95. To better understand the molecular mechanism of this enzyme, we determined the x-ray crystal structures of the AfcA catalytic (Fuc) domain in unliganded and complexed forms with deoxyfuconojirimycin (inhibitor), 2'-fucosyllactose (substrate), and L-fucose and lactose (products) at 1.12-2.10 A resolution. The AfcA Fuc domain is composed of four regions, an N-terminal beta region, a helical linker, an (alpha/alpha)6 helical barrel domain, and a C-terminal beta region, and this arrangement is similar to bacterial phosphorylases. In the complex structures, the ligands were buried in the central cavity of the helical barrel domain. Structural analyses in combination with mutational experiments revealed that the highly conserved Glu566 probably acts as a general acid catalyst. However, no carboxylic acid residue is found at the appropriate position for a general base catalyst. Instead, a water molecule stabilized by Asn423 in the substrate-bound complex is suitably located to perform a nucleophilic attack on the C1 atom of L-fucose moiety in 2'-fucosyllactose, and its location is nearly identical near the O1 atom of beta-L-fucose in the products-bound complex. Based on these data, we propose and discuss a novel catalytic reaction mechanism of AfcA.

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

    Science.gov (United States)

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

    2016-08-17

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

  6. Study on the reaction of carbon disulfide with hydroxyl radical in aqueous solution

    Institute of Scientific and Technical Information of China (English)

    FANG Haojie; OUYANG Bin; QIN Yan; DONG Wenbo; HOU Huiqi

    2005-01-01

    The laser flash photolysis technique is employed to investigate the reaction mechanism of CS2 with ·OH in the nitrogen-saturated aqueous solution. By comparison of the transient absorption spectra obtained at different phases and pHs and through the addition of proper radical cation scavenger, CS2 is determined to react with ·OH to form ·CS2OH adduct, instead of the CS2+ radical cation. At pH 1-5, ·CS2OH decomposes into COS and ·HS, while at pH>5, it further reacts with OH- to form CS2O-. The temperature dependent kinetics for the reaction CS2 + ·OH →·CS2OH is also reported in this paper with an estimated activation energy of (26.9±1.0) kJ·mol1.

  7. Improving the durability of methanol oxidation reaction electro-catalysts through the modification of carbon architectures

    Science.gov (United States)

    Wood, Kevin N.

    Carbon materials represent one of the largest areas of studied research today, having integrated applications stretching from energy production and storage to medical use and far beyond. One of these many intriguing applications is fuel cells, which offers the promise of clean electricity through a direct electrochemical energy conversion process. Unfortunately, at the present time the cost per watt-hour produced by fuel cells is more expensive than conventional methods of energy production/storage (i.e. combustion engines, batteries, etc.). Under the umbrella of fuel cell systems, methanol is a promising fuel source because of its high energy density and convenience of direct liquid fuel operation. In this field, recent advancements are bringing direct methanol fuel cells (DMFCs) closer to commercial viability. However, just as in other fuel cell systems, further improvements are greatly needed, particularly in the area of catalyst durability. This need for improved durability has led to increased research activity focused on improving catalyst stability and utilization. This thesis explores one of the most promising areas of enhancing catalyst-support interactions; namely, modification of carbon support architectures. Through the use of heteroatom modifiers, such as nitrogen, fuel cell support systems can be enhanced in such a way as to improve metal nucleation and growth, catalyst durability and catalytic activity. To this end, this thesis employs advanced characterization techniques to study the changes in catalyst particle morphology before and after nitrogen modification of the support structure. These results clearly show the beneficial effects of nitrogen moieties on carbon structures and help elucidate the effects of nitrogen on the stability of supported catalytic nanoparticles systems. Similarly, the novel concept of post-modifying commercially available supported catalysts with nitrogen ion implantation gives further insight into the behavior of

  8. Backward emitted high-energy neutrons in hard reactions of p and pi^+ on carbon

    OpenAIRE

    Malki, A.; Alster, J.; Asryan, G.; Barton, D; Baturin, V.; Buchkojarova, N.; Carroll, A.; Chtchetkovski, A.; Heppelmann, S.; Kawabata, T.; Leksanov, A.; Makdisi, Y.; Minina, E.; Navon, I.; Nicholson, H.

    2000-01-01

    Beams of protons and pions of 5.9 GeV/c were incident on a C target. Neutrons emitted into the back hemisphere, in the laboratory system, were detected in (triple) coincidence with two emerging $p_t>$0.6 GeV/c particles. We present the momentum spectra of the backward going neutrons, which have the same universal shape observed in earlier (inclusive) reactions induced by hadrons, $\\gamma$, $\

  9. Assessment of the apparent activation energies for gas/solid reactions-carbonate decomposition

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The guidelines for assessing the apparent activation energies of gas/solid reactions have been proposed based on the ex-perimental results from literatures. In CO2 free inlet gas flow, CaCO3 decomposition between 950 and 1250 K with thin sample layercould be controlled by the interfacial chemical reaction with apparent activation energy E = (215+10) kJ/mol and E = (200±10)kJ/mol at T = 813 to 1020 K, respectively. With relatively thick sample layer between 793 and 1273 K, the CaCO3 decompositioncould be controlled by one or more steps involving self-cooling, nucleation, intrinsic diffusion and heat transfer of gases, and E couldvary between 147 andl90 kJ/mol. In CO2 containing inlet gas flow (5%-100% of CO2), E was determined to be varied from 949 to2897 kJ/mol. For SrCO3 and BaCO3 decompositions controlled by the interfacial chemical reaction, E was (213+15) kJ/mol (1000-1350 K) and (305+15) kJ/mol (1260-1400 K), respectively.

  10. Neon-matrix spectroscopic and theoretical studies of the reactivity of titanium dimer with diatomic ligands: comparison of reactions with nitrogen and carbon monoxide.

    Science.gov (United States)

    Souvi, S M; Berkaïne, N; Alikhani, M E; Manceron, L

    2009-11-14

    The reactivity of diatomic titanium with molecular carbon monoxide has been investigated in solid neon at very low temperature. In contrast to the spontaneous reaction observed between Ti(2) and N(2), our results show that the formation of dititanium oxycarbide (OTi(2)C) from the condensation of effusive beams of Ti and CO in neon matrices involves several intermediate steps including one metastable intermediate. In the absence of electronic excitation, only formation of a Ti(2)(CO) complex occurs spontaneously during the reaction at 9 K of ground state Ti(2) and CO, as reported in solid argon by Xu, Jiang and Tsumori (Angew. Chem. Int. Ed., 2005, 44, 4338). However, during deposition or following electronic excitation, this species rearranges into a new species: the more stable, OTi(2)C oxycarbide form. Several low-lying excited states of OTi(2)C are also observed between 0.77 and 0.89 eV above the ground state, leading to a complex sequence of interacting vibronic transitions, merging into a broad continuum above 1 eV. Observations of Ti(2)(12)C(16)O, Ti(2)(13)C(16)O and Ti(2)(12)C(18)O and natural titanium isotopic data enable the identification of four fundamental vibrations in the ground electronic state and two others in the first two excited states. Quantum chemical calculations predict an open-shell (1)A(g) ground state with Ti-C and Ti-O distances close to 184 pm, and 91 degrees for the TiCTi and TiOTi bond angles, and give fundamental frequencies in good agreement with observation. The reaction paths of the Ti(2) + N(2) --> Ti(2)N(2) and Ti(2) + CO --> Ti(2)(CO) --> OTi(2)C have been investigated and a reaction scheme is proposed accounting for the similarities in nature and properties of the final products, as well as explaining the observation of a coordination complex with Ti(2) only in the case of the carbonyl ligand.

  11. (π±, π±' N) reactions on 12C and 208Pb near the giant resonance region

    International Nuclear Information System (INIS)

    Angular distributions for the 12C(π±, π±' p) and 208Pb(π±, π±' p or n) reactions near the giant resonance region have been measured at Tπ = 180 MeV, and found different between π+ and π- data. This observation is interpreted as evidence for different excitation mechanisms dominating the π--nucleus and π+-nucleus interactions in the giant resonance region of these targets. A comparison with the single-nucleon knock-out distorted-wave impulse approximation calculations shows, even though these calculations underestimate (π±, π±' N) data for both targets, the dominance of direct process for (π+, π+' p) or (π-, π-' n) in contrast to (π-, π-' p) or (π+, π+' n). In the (π+, π+' p) reaction proton-proton hole states are excited directly and appear to have a large probability for direct decay with escape width, whereas in (π-, π-' p) the preferentially excited neutron-neutron hole doorway states couple to resonance states and decay with spreading width. This interpretation led us to suggest that the ratio of cross-sections for inelastic scattering to the giant resonance region should be written in terms of an incoherent sum of cross-sections to neutron and proton doorway states. In a heavy nucleus such as 208Pb, neutron and proton doorway states. In a heavy nucleus such as 208Pb, neutron and proton doorway states contribute incoherently because the different decay processes do not populate the same final states of the residual nucleus

  12. Removal of Direct Yellow-12 Dye from Water by Adsorption on Activated Carbon Prepared from Ficus Racemosa L.

    OpenAIRE

    Revathi, G.; Ramalingam, S; P. Subramaniam; A. Ganapathi

    2011-01-01

    The adsorption of direct yellow-12 dye (DY-12) by Atti leaf (Ficus racemosa) powder carbon (ATC) was carried out by varying the parameters such as agitation time, dye concentration, adsorbent dose, pH and temperature. Equilibrium adsorption data followed both Langmuir and Freundlich isotherms. Adsorption followed second-order kinetics. The adsorption capacity was found to be 6.7 mg dye per gram of the adsorbent. Acidic pH was favorable for the adsorption of DY-12. Desorption studies suggest t...

  13. Thermophysical properties and reaction kinetics of γ-irradiated poly allyl diglycol carbonates nuclear track detector

    Science.gov (United States)

    Elmaghraby, Elsayed K.; Seddik, Usama

    2015-07-01

    Kinetic thermogravimetric technique was used to study the effect of gamma irradiation on the poly allyl diglycol carbonates (PADC) within the dose range from 50 to ? Gy. The approach of Coats-Redfern was used to analyze the data. Results showed that low doses around 50 Gy make the polymer slightly more resistive to heat treatment. Higher radiation doses cause severe effects in the samples accompanied by the formation of lower molecular mass species and consequent crosslinking. Results support the domination of re-polymerization and crosslinking for the γ radiation interaction PADC at dose below about ? Gy, while the situation is inverted above ? Gy in which chain secession dominates.

  14. Carbon dioxide activation and reaction induced by electron transfer at an oxide-metal interface.

    Science.gov (United States)

    Calaza, Florencia; Stiehler, Christian; Fujimori, Yuichi; Sterrer, Martin; Beeg, Sebastian; Ruiz-Oses, Miguel; Nilius, Niklas; Heyde, Markus; Parviainen, Teemu; Honkala, Karoliina; Häkkinen, Hannu; Freund, Hans-Joachim

    2015-10-12

    A model system has been created to shuttle electrons through a metal-insulator-metal (MIM) structure to induce the formation of a CO2 anion radical from adsorbed gas-phase carbon dioxide that subsequently reacts to form an oxalate species. The process is completely reversible, and thus allows the elementary steps involved to be studied at the atomic level. The oxalate species at the MIM interface have been identified locally by scanning tunneling microscopy, chemically by IR spectroscopy, and their formation verified by density functional calculations.

  15. Fossil and Contemporary Fine Carbon Fractions at 12 Rural and Urban Sites in the United States

    Energy Technology Data Exchange (ETDEWEB)

    Schichtel, B; Malm, W; Bench, G; Fallon, S; McDade, C; Chow, J

    2007-03-01

    Fine particulate matter collected at two urban, four near-urban, and six remote sites throughout the United States were analyzed for total carbon (TC) and radiocarbon ({sup 14}C). Samples were collected at most sites for both a summer and winter season. The radiocarbon was used to partition the TC into fossil and contemporary fractions. On average, contemporary carbon composed about half of the carbon at the urban, {approx}70-97% at near-urban, and 82-100% at remote sites. At Phoenix, Arizona, and Seattle, Washington, one monitor was located within the urban center and one outside to assess the urban excess over background concentrations. During the summer the urban and rural sites had similar contemporary carbon concentrations. However, during the winter the urban sites had more than twice the contemporary carbon measured at the neighboring sites, indicating anthropogenic contributions to the contemporary carbon. The urban fossil carbon was 4-20 times larger than the neighboring rural sites for both seasons. Organic (OC) and elemental carbon (EC) from TOR analysis were available. These and the radiocarbon data were used to estimate characteristic fossil and contemporary EC/TC ratios for the winter and summer seasons. These ratios were applied to carbon data from the Interagency Monitoring of Protected Visual Environments network to estimate the fraction of contemporary carbon at mostly rural sites throughout the United States. In addition, the ratios were used to develop a semiquantitative, lower bound estimate of secondary organic carbon (SOC) contribution to fossil and contemporary carbon. SOC accounted for more than one-third of the fossil and contemporary carbon.

  16. A palladium-doped ceria@carbon core-sheath nanowire network: a promising catalyst support for alcohol electrooxidation reactions

    Science.gov (United States)

    Tan, Qiang; Du, Chunyu; Sun, Yongrong; Du, Lei; Yin, Geping; Gao, Yunzhi

    2015-08-01

    A novel palladium-doped ceria and carbon core-sheath nanowire network (Pd-CeO2@C CSNWN) is synthesized by a template-free and surfactant-free solvothermal process, followed by high temperature carbonization. This hierarchical network serves as a new class of catalyst support to enhance the activity and durability of noble metal catalysts for alcohol oxidation reactions. Its supported Pd nanoparticles, Pd/(Pd-CeO2@C CSNWN), exhibit >9 fold increase in activity toward the ethanol oxidation over the state-of-the-art Pd/C catalyst, which is the highest among the reported Pd systems. Moreover, stability tests show a virtually unchanged activity after 1000 cycles. The high activity is mainly attributed to the superior oxygen-species releasing capability of Pd-doped CeO2 nanowires by accelerating the removal of the poisoning intermediate. The unique interconnected one-dimensional core-sheath structure is revealed to facilitate immobilization of the metal catalysts, leading to the improved durability. This core-sheath nanowire network opens up a new strategy for catalyst performance optimization for next-generation fuel cells.A novel palladium-doped ceria and carbon core-sheath nanowire network (Pd-CeO2@C CSNWN) is synthesized by a template-free and surfactant-free solvothermal process, followed by high temperature carbonization. This hierarchical network serves as a new class of catalyst support to enhance the activity and durability of noble metal catalysts for alcohol oxidation reactions. Its supported Pd nanoparticles, Pd/(Pd-CeO2@C CSNWN), exhibit >9 fold increase in activity toward the ethanol oxidation over the state-of-the-art Pd/C catalyst, which is the highest among the reported Pd systems. Moreover, stability tests show a virtually unchanged activity after 1000 cycles. The high activity is mainly attributed to the superior oxygen-species releasing capability of Pd-doped CeO2 nanowires by accelerating the removal of the poisoning intermediate. The unique

  17. TiO2-sludge carbon enhanced catalytic oxidative reaction in environmental wastewaters applications.

    Science.gov (United States)

    Athalathil, Sunil; Erjavec, Boštjan; Kaplan, Renata; Stüber, Frank; Bengoa, Christophe; Font, Josep; Fortuny, Agusti; Pintar, Albin; Fabregat, Azael

    2015-12-30

    The enhanced oxidative potential of sludge carbon/TiO2 nano composites (SNCs), applied as heterogeneous catalysts in advanced oxidation processes (AOPs), was studied. Fabrification of efficient SNCs using different methods and successful evaluation of their catalytic oxidative activity is reported for the first time. Surface modification processes of hydrothermal deposition, chemical treatment and sol-gel solution resulted in improved catalytic activity and good surface chemistry of the SNCs. The solids obtained after chemical treatment and hydrothermal deposition processes exhibit excellent crystallinity and photocatalytic activity. The highest photocatalytic rate was obtained for the material prepared using hydrothermal deposition technique, compared to other nanocomposites. Further, improved removal of bisphenol A (BPA) from aqueous phase by means of catalytic ozonation and catalytic wet air oxidation processes is achieved over the solid synthesized using chemical treatment method. The present results demonstrate that the addition of TiO2 on the surface of sludge carbon (SC) increases catalytic oxidative activity of SNCs. The latter produced from harmful sludge materials can be therefore used as cost-effective and efficient sludge derived catalysts for the removal of hazardous pollutants. PMID:26223014

  18. Localized surface grafting reactions on carbon nanofibers induced by gamma and e-beam irradiation

    Science.gov (United States)

    Evora, M. C.; Araujo, J. R.; Ferreira, E. H. M.; Strohmeier, B. R.; Silva, L. G. A.; Achete, C. A.

    2015-04-01

    Electron beam and gamma-ray irradiation have potential application to modify the carbon fiber nanostructures in order to produce useful defects in the graphitic structure and create reactive sites. In this study, the methodology to functionalize carbon nanofiber (CNF), via a radiation process and using acrylic acid as a source of oxygen functional groups, was investigated. The samples were submitted to a direct grafting radiation process with electron beam and gamma-ray source. Several parameters were changed such as: acrylic acid concentration, radiation dose and percentage of inhibitor necessary to achieve functionalization, with higher percentage of oxygen functional groups on CNF surface, and better dispersion. The better results achieved were when mixing CNF in a solution of acrylic acid with 6% of inhibitor (FeSO4·7H2O) and irradiated at 100 kGy. The samples were characterized by X-ray photoelectron spectroscopy and the surface composition (atomic%) showed a significant increase of oxygen content for the samples after irradiation. Also, the dispersion of the functionalized CNF in water was stable during months which may be a good indication that the functionalization process of CNF via ionizing radiation was successful.

  19. Dissolved Organic Carbon Determination Using FIA and Photo-Fenton Reaction

    Directory of Open Access Journals (Sweden)

    Kondo Márcia M.

    2002-01-01

    Full Text Available The FIA-photo-Fenton system is based on the flow oxidation of the organic matter. A small amount of the sample containing H2O2 is injected into the acidic flow solution of Fe2+, which passes through a tubular PTFE reactor irradiated with UV light. The generated CO2 is quantified by a conductometric detector and is directly proportional to the dissolved organic carbon concentration in the sample. The optimization studies were performed using EDTA solutions. The average recovery of organic carbon was 83% with a relative standard deviation of 3.7% using a 1:5 molar ratio of Fe2+:H2O2, pH 2.0, 100 muL of sample injection and a liquid flow of 1 mL min-1. After optimization, the DOC concentration was quantified using 13 different organic compounds, where the average recovery was 90%. The rate of the analysis was in average 50 samples hour-1.

  20. Transition Metal Catalyzed Reactions for Forming Carbon–Oxygen and Carbon–Carbon Bonds

    DEFF Research Database (Denmark)

    Sølvhøj, Amanda Birgitte

    , using the radical precursor as solvent, in the presence of 10–12 % of MnCl2, and refluxing overnight in the presence of air. A simple acidic workup and purification by chromatography yielded the products in moderate to good yield. The radical precursor can be a cyclic or acyclic ether or even...

  1. Ga(ClO4)3-catalyzed Reaction of 1,2-Diamines and α-Bromoketones: Synthesis of 2-Substituted Quinoxalines

    Institute of Scientific and Technical Information of China (English)

    JI Yun-fei; CHEN Tang-ming; MAO Hai-feng; ZOU Jian-ping

    2012-01-01

    Ga(ClO4)3-catalyzed reaction of 1,2-aryldiamines and a-bromoketones to afford 2-substituted quinoxalines in good yields is described.The reaction proceeded via grinding process with 10%(molar fraction) catalyst under solvent-free conditions at room temperature.For unsymmetrical o-phenylenediamines bearing electron-withdrawing groups,regio-selective quinoxalines were obtained.

  2. STUDIES ON THE CATALYTIC REACTION OF NITROGEN OXIDE ON METAL MODIFIED ACTIVATED CARBON FIBERS

    Institute of Scientific and Technical Information of China (English)

    FU Ruowen; DU Xiuying; LIN Yuansheng; XU Hao; HU Yiongjun

    2003-01-01

    The catalytic reaction of NO with CO and decomposition of NO over metal modified ACFs were investigated and compared with other carriers supported catalysts. It is demonstrated that Pd/ACF and Pd/Cu/ACF have high catalytic activity for the reaction of NO/CO, while Pt/ACF.Pt/Cu/ACF and Co/Cu/ACF have very Iow catalytic activity in similar circumstance. Pd-modified ACF possesses high catalytic decomposition of NO at 300 ℃. Pd/CB and Pd/GAC present good catalytic decomposition ability for NO only at low flowrate. Pd/G, Pd/ZMS and Pd/A however, do not show any catalytic activity for NO decomposition even at 400 ℃. Catalytic temperature, NO flowrate and loading of metal components affect the decomposition rate of NO. The coexistence of Cu with Pd on Cu/Pd/ACF leads to crystalline of palladium to more unperfected so as to that increase the catalytic activity.

  3. Preliminary study of the missing mass spectra via the $^{12}C(p, K^0_s)$ and $^{12}C(p,\\Lambda)$ reactions at 10 GeV/c

    CERN Document Server

    Aslanyan, P Zh

    2012-01-01

    The missing mass spectra for the $^{12}C(p, K^0_s)$ and $^{12}C(p,\\Lambda)$ reactions have been studied by using of the propane bubble chamber(PBC) data from 700000 stereo photographs or $10^6$ inelastic interactions. The momentum spectrum of $\\pi^-$ in range of 100-200 MeV/c have observed the significant enhancement from the p+C$\\to \\pi^-\\Lambda$X(p+C$\\to\\pi^-K^0_s$X) reaction. The missing mass spectra have been observed signals for the $p(p,\\pi^-K^0_s)$, $^3H(p,pK^0_s)$, p(p,$\\Lambda)\\pi^-\\gamma$ and p(p,$\\pi^-)\\Lambda$ reactions. This experimental study will need to continue by using of a different identification methods for a reaction channels.

  4. Estimation of the breakup cross sections in $^6$He+$^{12}$C reaction within high-energy approximation and microscopic optical potential

    CERN Document Server

    Zemlyanaya, E V; Lukyanov, K V

    2010-01-01

    The breakup cross sections in the reaction $^6$He+$^{12}$C are calculated at about 40 MeV/nucleon using the high-energy approximation (HEA) and with the help of microscopic optical potentials (OP) of interaction with the target nucleus $^{12}$C of the projectile nucleus fragments $^4$He and 2n. Considering the di-neutron $h$=2n as a single particle the relative motion $h\\alpha$ wave function is estimated so that to explain both the separation energy of $h$ in $^6$He and the rms radius of the latter. The stripping and absorbtion total cross sections are calculated and their sum is compared with the total reaction cross section obtained within a double-folding microscopic OP for the $^6$He+$^{12}$C scattering. It is concluded that the breakup cross sections contribute in about 50% of the total reaction cross section.

  5. Synthesis of Bridged Heterocycles via Sequential 1,4- and 1,2-Addition Reactions to α,β-Unsaturated N-Acyliminium Ions: Mechanistic and Computational Studies.

    Science.gov (United States)

    Yazici, Arife; Wille, Uta; Pyne, Stephen G

    2016-02-19

    Novel tricyclic bridged heterocyclic systems can be readily prepared from sequential 1,4- and 1,2-addition reactions of allyl and 3-substituted allylsilanes to indolizidine and quinolizidine α,β-unsaturated N-acyliminium ions. These reactions involve a novel N-assisted, transannular 1,5-hydride shift. Such a mechanism was supported by examining the reaction of a dideuterated indolizidine, α,β-unsaturated N-acyliminium ion precursor, which provided specifically dideuterated tricyclic bridged heterocyclic products, and from computational studies. In contrast, the corresponding pyrrolo[1,2-a]azepine system did not provide the corresponding tricyclic bridged heterocyclic product and gave only a bis-allyl adduct, while more substituted versions gave novel furo[3,2-d]pyrrolo[1,2-a]azepine products. Such heterocyclic systems would be expected to be useful scaffolds for the preparation of libraries of novel compounds for new drug discovery programs. PMID:26816207

  6. An electrochemical immunosensor based on covalent immobilization of okadaic acid onto screen printed carbon electrode via diazotization-coupling reaction.

    Science.gov (United States)

    Hayat, Akhtar; Barthelmebs, Lise; Sassolas, Audrey; Marty, Jean-Louis

    2011-07-15

    In this work, an electrochemical method based on the diazonium-coupling reaction mechanism for the immobilization of okadaic acid (OA) on screen printed carbon electrode was developed. At first, 4-carboxyphenyl film was grafted by electrochemical reduction of 4-carboxyphenyl diazonium salt, followed by terminal carboxylic group activation by N-hydroxysuccinimide (NHS), N-(3-dimethylaminopropyle)-N'-ethyle-carbodiimide hydrochloride (EDC). Hexamethyldiamine was then covalently bound by one of its terminal amine group to the activated carboxylic group. The carboxyl group of okadaic acid was activated by EDC/NHS and then conjugated to the second terminal amine group on other side of the hexamethyldiamine through amide bond formation. After immobilization of OA, an indirect competitive immunoassay format was employed to detect OA. The immunosensor obtained using this novel approach allowed detection limit of 1.44 ng/L of OA, and was also validated with certified reference mussel samples. PMID:21645734

  7. Differential cross section, tensor Ayy and vector Ay analyzing power in the 12C(d, p)X reaction at 9 GeV/c and 85 mrad emission angle of protons

    International Nuclear Information System (INIS)

    The experimental data on the differential cross section, tensor Ayy and vector Ay analyzing powers in the deuteron breakup reaction on carbon 12C(d, p)X obtained at initial momenta 9 GeV/c and 85 mr emission angle of protons are presented. While the differential cross section is satisfactorily described within the framework of the hard scattering model using conventional deuteron wave functions, the behaviour of the tensor analyzing power Ayy, which remains positive up to the highest measured momenta of protons, is in disagreement with the predictions of this model. The non-zero values of the vector analyzing power Ay can indicate that the spin-dependent part of the nucleon-nucleon amplitude can be significant in the mechanism of this reaction. Simultaneously, the data on the differential cross section, Ayy and Ay in the 12C(d, p)X reaction in the vicinity of missing masses ∼ 2.2 GeV/c are obtained

  8. World Carbon Black Output to Reach 12.7 Million Tons in 2015

    Institute of Scientific and Technical Information of China (English)

    Zhu Yongkang

    2012-01-01

    From April 13 to April 17, "Carbon Black China of 2012" (CBC2012) was held in Hangzhou, China. Mr. Paul Ita, the president of US marketing research institution Notch Consulting Group, announced that the prospect of carbon black industry was closely linked with the development of auto industry and tire industry. The demand for carbon black of 2010 increased by 15% compared with that of 2009; the growth rate of demand for carbon black was 5.8% in 2011 and the total output was 10.7 million tons, which increased by about 5.5% compared with that of 2010.

  9. Reaction of carbon tetrachloride with methane in a non-equilibrium plasma at atmospheric pressure, and characterisation of the polymer thus formed.

    Science.gov (United States)

    Gaikwad, Vaibhav; Kennedy, Eric; Mackie, John; Holdsworth, Clovia; Molloy, Scott; Kundu, Sazal; Stockenhuber, Michael; Dlugogorski, Bogdan

    2014-09-15

    In this paper we focus on the development of a methodology for treatment of carbon tetrachloride utilising a non-equilibrium plasma operating at atmospheric pressure, which is not singularly aimed at destroying carbon tetrachloride but rather at converting it to a non-hazardous, potentially valuable commodity. This method encompasses the reaction of carbon tetrachloride and methane, with argon as a carrier gas, in a quartz dielectric barrier discharge reactor. The reaction is performed under non-oxidative conditions. Possible pathways for formation of major products based on experimental results and supported by quantum chemical calculations are outlined in the paper. We elucidate important parameters such as carbon tetrachloride conversion, product distribution, mass balance and characterise the chlorinated polymer formed in the process.

  10. G64-12 and G64-37 are Carbon-Enhanced Metal-Poor Stars

    CERN Document Server

    Placco, Vinicius M; Reggiani, Henrique; Melendez, Jorge

    2016-01-01

    We present new high-resolution chemical-abundance analyses for the well-known high proper-motion subdwarfs G64-12 and G64-37, based on very high signal-to-noise spectra (S/N ~ 700/1) with resolving power R ~ 95,000. These high-quality data enable the first reliable determination of the carbon abundances for these two stars; we classify them as carbon-enhanced metal-poor (CEMP) stars based on their carbonicities, which both exceed [C/Fe] = +1.0. They are sub-classified as CEMP- no Group-II stars, based on their location in the Yoon-Beers diagram of absolute carbon abundance, A(C) vs. [Fe/H], as well as on the conventional diagnostic [Ba/Fe]. The relatively low absolute carbon abundances of CEMP-no stars, in combination with the high effective temperatures of these two stars (Teff ~ 6500 K) weakens their CH molecular features to the point that accurate carbon abundances can only be estimated from spectra with very high S/N. A comparison of the observed abundance patterns with the predicted yields from massive, ...

  11. Reaction of erythromycin with dissolved oxygen on gold nanoparticle-modified glassy carbon electrodes

    Institute of Scientific and Technical Information of China (English)

    LI Xue; FU Ying; WANG Jian-xiu; L(U) Hui-dan; XU Mao-tian

    2008-01-01

    Cyclic voltammetry was used to investigate the reaction of erythromycin (EM) with dissolved oxygen on gold nanoparticle-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V and a reoxidation peak at -0.055V were observed. With the addition of EM into the NaOH solution containing dissolved oxygen, the oxidation peak at -0.055 V was still indiscernible. However, a new oxidation peak at 0.200V appeared, which suggests the interaction between EM and dissolved oxygen. Therefore, this method can be used for the analysis of EM in tablets. The present method is simple, reproducible,and does not require complex analytical instruments.

  12. Rates of hydroxyl radical reactions with some HFCs. [HydroFluoroCarbons

    Science.gov (United States)

    Demore, William B.

    1993-01-01

    Relative rate constants for OH reactions with some HFCs have been determined at 298 K by a technique which measures the loss of HFC greater than OH. The following ratios were determine: k(152a)/k(CH4) = 5.2 +/- 0.5, k(CH4)/k(125) = 3.9 +/- 0.5, k(CH4)/k(134a) = 2.1 +/- 0.2, k(134a)/k(125) = 2.0 +/- 0.2, and k(C2H6)/k(152a) = 6.2 +/- 1.0. These results are in good agreement with literature values for the absolute rate constants except for HFC 134a, where a slower rate constant is indicated.

  13. Gas/solid carbon branching ratios in surface-mediated reactions and the incorporation of carbonaceous material into planetesimals

    Science.gov (United States)

    Nuth, Joseph A.; Johnson, Natasha M.; Ferguson, Frank T.; Carayon, Alicia

    2016-07-01

    We report the ratio of the initial carbon available as CO that forms gas-phase compounds compared to the fraction that deposits as a carbonaceous solid (the gas/solid branching ratio) as a function of time and temperature for iron, magnetite, and amorphous iron silicate smoke catalysts during surface-mediated reactions in an excess of hydrogen and in the presence of N2. This fraction varies from more than 99% for an amorphous iron silicate smoke at 673 K to less than 40% for a magnetite catalyst at 873 K. The CO not converted into solids primarily forms methane, ethane, water, and CO2, as well as a very wide range of organic molecules at very low concentration. Carbon deposits do not form continuous coatings on the catalytic surfaces, but instead form extremely high surface area per unit volume "filamentous" structures. While these structures will likely form more slowly but over much longer times in protostellar nebulae than in our experiments due to the much lower partial pressure of CO, such fluffy coatings on the surfaces of chondrules or calcium aluminum inclusions could promote grain-grain sticking during low-velocity collisions.

  14. Gas/solid carbon branching ratios in surface-mediated reactions and the incorporation of carbonaceous material into planetesimals

    Science.gov (United States)

    Nuth, Joseph A.; Johnson, Natasha M.; Ferguson, Frank T.; Carayon, Alicia

    2016-06-01

    We report the ratio of the initial carbon available as CO that forms gas-phase compounds compared to the fraction that deposits as a carbonaceous solid (the gas/solid branching ratio) as a function of time and temperature for iron, magnetite, and amorphous iron silicate smoke catalysts during surface-mediated reactions in an excess of hydrogen and in the presence of N2. This fraction varies from more than 99% for an amorphous iron silicate smoke at 673 K to less than 40% for a magnetite catalyst at 873 K. The CO not converted into solids primarily forms methane, ethane, water, and CO2, as well as a very wide range of organic molecules at very low concentration. Carbon deposits do not form continuous coatings on the catalytic surfaces, but instead form extremely high surface area per unit volume "filamentous" structures. While these structures will likely form more slowly but over much longer times in protostellar nebulae than in our experiments due to the much lower partial pressure of CO, such fluffy coatings on the surfaces of chondrules or calcium aluminum inclusions could promote grain-grain sticking during low-velocity collisions.

  15. Stereoselective synthesis of C-fused pyranoindoles, pyranobenzofurans and pyranobenzothiophene scaffolds using oxa-Pictet-Spengler type reaction of vinylogous carbonates.

    Science.gov (United States)

    Gharpure, Santosh J; Prasath, V

    2014-10-01

    C-fused pyranoheterocycles can be readily assembled using an intramolecular oxa-Pictet-Spengler type reaction of vinylogous carbonates in a highly stereoselective manner. Required indole and benzofuran rings tethered to vinylogous carbonates are prepared by a tandem Sonogashira coupling-nucleopalladation reaction. The entire process can also be carried out in a 'one-pot' manner starting from homopropargyl alcohol. The C-fused pyranoindoles could be converted to spirooxindoles as well as to ring expanded products under oxidative conditions. PMID:25137156

  16. 40 CFR 600.208-12 - Calculation of FTP-based and HFET-based fuel economy and carbon-related exhaust emission values...

    Science.gov (United States)

    2010-07-01

    ...-based fuel economy and carbon-related exhaust emission values for a model type. 600.208-12 Section 600.208-12 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) ENERGY POLICY FUEL ECONOMY AND CARBON-RELATED EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy Regulations for 1977 and...

  17. 40 CFR 600.206-12 - Calculation and use of FTP-based and HFET-based fuel economy and carbon-related exhaust emission...

    Science.gov (United States)

    2010-07-01

    ... HFET-based fuel economy and carbon-related exhaust emission values for vehicle configurations. 600.206-12 Section 600.206-12 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) ENERGY POLICY FUEL ECONOMY AND CARBON-RELATED EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy Regulations...

  18. Radiosensitivity of pimonidazole-unlabelled intratumour quiescent cell population to γ-rays, accelerated carbon ion beams and boron neutron capture reaction.

    OpenAIRE

    Masunaga, S; Sakurai, Y.; Tanaka, H.; Hirayama, R; Matsumoto, Y; Uzawa, A; Suzuki, M.; Kondo, N; Narabayashi, M.; Maruhashi, A; Ono, K.

    2013-01-01

    [Objectives] To detect the radiosensitivity of intratumour quiescent (Q) cells unlabelled with pimonidazole to accelerated carbon ion beams and the boron neutron capture reaction (BNCR). [Methods] EL4 tumour-bearing C57BL/J mice received 5-bromo-2′-deoxyuridine (BrdU) continuously to label all intratumour proliferating (P) cells. After the administration of pimonidazole, tumours were irradiated with γ-rays, accelerated carbon ion beams or reactor neutron beams with the prior administration of...

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

    KAUST Repository

    Isogai, Shunsuke

    2011-11-30

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

  20. Structure of carbon-supported Pt-Ru nanoparticles and their electrocatalytic behavior for hydrogen oxidation reaction

    Energy Technology Data Exchange (ETDEWEB)

    Velazquez, Amado; Centellas, Francesc; Garrido, Jose Antonio; Arias, Conchita; Rodriguez, Rosa Maria; Brillas, Enric; Cabot, Pere-Lluis [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2010-02-01

    The electrochemical activity towards hydrogen oxidation reaction (HOR) of a high performance carbon-supported Pt-Ru electrocatalyst (HP 20 wt.% 1:1 Pt-Ru alloy on Vulcan XC-72 carbon black) has been studied using the thin-film rotating disk electrode (RDE) technique. The physical properties of the Pt-Ru nanoparticles in the electrocatalyst were previously determined by transmission electron microscopy (TEM), high resolution TEM, fast Fourier transform (FFT), electron diffraction and X-ray diffraction (XRD). The corresponding compositional and size-shape analyses indicated that nanoparticles generally presented a 3D cubo-octahedral morphology with about 26 at.% Ru in the lattice positions of the face-centred cubic structure of Pt. The kinetics for HOR was studied in a hydrogen-saturated 0.5 M H{sub 2}SO{sub 4} solution using thin-film electrodes prepared by depositing an ink of the electrocatalyst with different Nafion contents in a one-step process on a glassy carbon electrode. A maximum electrochemically active surface area (ECSA) of 119 m{sup 2} g Pt{sup -1} was found for an optimum Nafion composition of the film of about 35 wt.%. The kinetic current density in the absence of mass transfer effects was 21 mA cm{sup -2}. A Tafel slope of 26 mV dec{sup -1}, independent of the rotation rate and Nafion content, was always obtained, evidencing that HOR behaves reversibly. The exchange current density referred to the ECSA of the Pt-Ru nanoparticles was 0.17 mA cm{sup -2}, a similar value to that previously found for analogous inks containing pure Pt nanoparticles. (author)

  1. Nitrogen-doped carbon dots originating from unripe peach for fluorescent bioimaging and electrocatalytic oxygen reduction reaction.

    Science.gov (United States)

    Atchudan, Raji; Edison, Thomas Nesakumar Jebakumar Immanuel; Lee, Yong Rok

    2016-11-15

    This paper reports the robust hydrothermal synthesis of nitrogen doped carbon dots (N-CDs) using the unripe fruit of Prunus persica (peach) as the carbon precursor and aqueous ammonia as the nitrogen source. The optical properties of synthesized N-CDs were characterized by ultraviolet visible (UV-Vis) and fluorescence spectroscopy techniques. The synthesized N-CDs were emitted blue light when excitated with a portable UV lamp. The materials with the optical properties were characterized further by high resolution transmission electron microscope (HRTEM), X-ray diffraction (XRD), Raman, Fourier transform infrared (FT-IR) and X-ray photoelectron spectroscopy (XPS). The mean size of the N-CDs was approximately 8nm, as calculated from the HRTEM image. The d-spacing of N-CDs, calculated using Bragg law, was approximately 0.21nm, which was consistent with the interlayer distance calculated from the HRTEM image. FT-IR spectroscopy and XPS revealed the presence of the phytoconstituents functionalities of peach fruit over the N-CDs surface and a high level of nitrogen doping on carbon dots (CDs) was confirmed by XPS studies. These results suggest that the unripe fruit extract of peach is an ideal candidate for the preparation of N-CDs. The resulting N-CDs showed excellent optical properties in water. The synthesized N-CDs exhibited a high fluorescence quantum yield and low cytotoxicity, and can be used as fluorescence imaging probes. In addition, the N-CDs were catalytically activite towards the oxygen reduction reaction (ORR). The N-CDs exhibited good catalytic activity in an alkaline medium (0.1M KOH) with a remarkable ORR of approximately 0.72V vs reversible hydrogen electrode (RHE), and O2 reduction follows mainly a 2 electron pathway by being reduced to hydrogen peroxide. The 2-electron reduction pathway is used in industry for H2O2 production. PMID:27479911

  2. Enantioselective organocatalyzed Oxa-Michael-Aldol cascade reactions: Construction of chiral 4H-chromenes with a trifluoromethylated tetrasubstituted carbon stereocenter

    KAUST Repository

    Zhang, Jing

    2015-03-13

    The first organocatalytic asymmetric synthesis of 4H-chromenes bearing a trifluoromethylated tetrasubstituted carbon center is presented. Chiral secondary amines promote the oxa-Michael-aldol cascade reaction between alkynals and 2-trifluoroacetylphenols via iminium-allenamine activation to produce pharmaceutically important heterocycles with excellent enantioselectivities. The proposed reaction can be scaled-up easily with maintenance of the excellent enantioselectivity. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. (. pi. sup +- ,. pi. sup +- prime N) reactions on sup 12 C and sup 208 Pb near the giant resonance region

    Energy Technology Data Exchange (ETDEWEB)

    Yoo, Sung Hoon.

    1990-05-01

    Angular distributions for the {sup 12}C({pi}{sup {plus minus}}, {pi}{sup {plus minus}}{prime} p) and {sup 208}Pb({pi}{sup {plus minus}}, {pi}{sup {plus minus}}{prime} p or n) reactions near the giant resonance region have been measured at T{sub {pi}} = 180 MeV, and found different between {pi}{sup +} and {pi}{sup {minus}} data. This observation is interpreted as evidence for different excitation mechanisms dominating the {pi}{sup {minus}}-nucleus and {pi}{sup +}-nucleus interactions in the giant resonance region of these targets. A comparison with the single-nucleon knock-out distorted-wave impulse approximation calculations shows, even though these calculations underestimate ({pi}{sup {plus minus}}, {pi}{sup {plus minus}}{prime} N) data for both targets, the dominance of direct process for ({pi}{sup +}, {pi}{sup {plus}}{prime} p) or ({pi}{sup {minus}}, {pi}{sup {minus}}{prime} n) in contrast to ({pi}{sup {minus}}, {pi}{sup {minus}}{prime} p) or ({pi}{sup +}, {pi}{sup +}{prime} n). In the ({pi}{sup +}, {pi}{sup +}{prime} p) reaction proton-proton hole states are excited directly and appear to have a large probability for direct decay with escape width, whereas in ({pi}{sup {minus}}, {pi}{sup {minus}}{prime} p) the preferentially excited neutron-neutron hole doorway states couple to resonance states and decay with spreading width. This interpretation led us to suggest that the ratio of cross-sections for inelastic scattering to the giant resonance region should be written in terms of an incoherent sum of cross-sections to neutron and proton doorway states. In a heavy nucleus such as {sup 208}Pb, neutron and proton doorway states. In a heavy nucleus such as {sup 208}Pb, neutron and proton doorway states contribute incoherently because the different decay processes do not populate the same final states of the residual nucleus.

  4. Electrochemical quartz crystal microbalance measurement of a Li4Ti5O12 composite electrode in a carbonate electrolyte

    Science.gov (United States)

    Serizawa, Nobuyuki; Shono, Kumi; Kobayashi, Yo; Miyashiro, Hajime; Katayama, Yasushi; Miura, Takashi

    2015-11-01

    Electrochemical quartz crystal microbalance (EQCM) measurement is conducted with a Li4Ti5O12 (lithium titanium oxide, LTO)-coated quartz crystal electrode in a carbonate electrolyte (ethylene carbonate + dimethyl carbonate; 50: 50 vol%) containing 1 M LiPF6. In-situ monitoring of the mass change during the charge and discharge of the LTO electrode can be achieved quantitatively because of the "zero-strain" property of LTO with Li+ insertion and the probably low reactivity between LTO and the electrolyte. The local changes of viscosity and density of the electrolyte contacting the LTO electrode are detected via the resonance resistance of the quartz crystal electrode, suggesting the local concentrations of Li+ and counter anion changed significantly during insertion and extraction of Li+ in the organic electrolyte.

  5. Chemiluminescence behavior of sodium hydrogen carbonate in the potassium permanganate-hydrogen peroxide reaction

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Chemiluminescence (CL) phenomenon of hydrogen peroxide with potassium permanganate in the presence of sodium hydrogen carbonate was reported.Effects of the surfactant on the CL system were investigated.Nonionic surfactants could effectively increase the CL signal.Radical scavengers and organic reagents such as nitro blue tetrazolium chloride (NBT),cytochrome c,sodium azide,ascorbic acid,thiourea,tert-butanol and dimethyl sulphoxide were used to study the emitting species.CL emission spectrum was recorded and the results showed that the maximal emission wavelengths of NaHCO3-H2O2-KMnO4 system were 440 and 634 nm.The mechanism was discussed based on electron spin resonance (ESR) spectra,fluorescence spectra and UV-vis absorption spectra.The addition of rhodamine B or uranine into this CL system enhanced the CL signal.It was due to part of the energy transfer from singlet oxygen and excited triplet dimers of two CO2 molecules to rhodamine B or uranine.The CL could be induced by excited rhodamine B or uranine.

  6. Crossed-beam reaction of carbon atoms with hydrocarbon molecules. V. Chemical dynamics of n-C4H3 formation from reaction of C(3Pj) with allene, H2CCCH2(X 1A1)

    Science.gov (United States)

    Kaiser, R. I.; Mebel, A. M.; Chang, A. H. H.; Lin, S. H.; Lee, Y. T.

    1999-06-01

    The crossed molecular beams technique was employed to investigate the reaction between ground state carbon atoms, C(3Pj), and allene, H2CCCH2(X 1A1), at two averaged collision energies of 19.6 and 38.8 kJ mol-1. Product angular distributions and time-of-flight spectra of C4H3 were recorded. Forward-convolution fitting of the data yields weakly polarized center-of-mass angular flux distributions isotropic at lower, but forward scattered with respect to the carbon beam at a higher collision energy. The maximum translational energy release and the angular distributions combined with ab initio and RRKM calculations are consistent with the formation of the n-C4H3 radical in its electronic ground state. The channel to the i-C4H3 isomer contributes less than 1.5%. Reaction dynamics inferred from the experimental data indicate that the carbon atom attacks the π-orbitals of the allenic carbon-carbon double bond barrierless via a loose, reactant-like transition state located at the centrifugal barrier. The initially formed cyclopropylidene derivative rotates in a plane almost perpendicular to the total angular momentum vector around its C-axis and undergoes ring opening to triplet butatriene. At higher collision energy, the butatriene complex decomposes within 0.6 ps via hydrogen emission to form the n-C4H3 isomer and atomic hydrogen through an exit transition state located 9.2 kJ mol-1 above the products. The explicit identification of the n-C4H3 radical under single collision represents a further example of a carbon-hydrogen exchange in reactions of ground state carbon atoms with unsaturated hydrocarbons. This channel opens a barrierless route to synthesize extremely reactive hydrocarbon radicals in combustion processes, interstellar chemistry, and hydrocarbon-rich atmospheres of Jupiter, Saturn, Titan, as well as Triton.

  7. Catalyst-free tandem Michael addition-cyclization reactions in aqueous media for the synthesis of benzimidazo[1,2-a]pyrimidinone derivatives

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The catalyst-free reactions of Baylis-Hillman alcohols (1a-i) with 2-aminobenzimidazole (2) in THF-H2O (1:4) were developed for the convenient and greener synthesis of benzimidazo[1,2-a]pyrimidinone derivatives (3a-i).The pesticidal activities of 3a-i were examined to investigate a new biological activity of the imidazo[1,2-a]pyrimidinone-type compounds.

  8. Backward emitted high-energy neutrons in hard reactions of p and π+ on carbon

    Science.gov (United States)

    Malki, A.; Alster, J.; Asryan, G.; Averichev, Y.; Barton, D.; Baturin, V.; Bukhtoyarova, N.; Carroll, A.; Heppelmann, S.; Kawabata, T.; Leksanov, A.; Makdisi, Y.; Minina, E.; Navon, I.; Nicholson, H.; Ogawa, A.; Panebratsev, Yu.; Piasetzky, E.; Schetkovsky, A.; Shimanskiy, S.; Tang, A.; Watson, J. W.; Yoshida, H.; Zhalov, D.

    2002-01-01

    Beams of protons and pions of 5.9 GeV/c were incident on a C target. Neutrons emitted into the backward hemisphere, in the laboratory system, were detected in (triple) coincidence with two emerging particles of tranverse momenta pt>0.6 GeV/c. We determined that for (46.5+/-3.7)% of the proton-induced events and for (40.8+/-4.5)% of the pion-induced events with the two high-pt particles, there is also at least one backward emitted neutron with momentum greater than 0.32 GeV/c. This observation is in sharp contrast to a well- established universal pattern from a large variety of earlier inclusive measurements with hadrons, electrons, photons, neutrinos, and antineutrinos where the probability for backward nucleon emission was in the 5 to 10 % range. We present also a measurement of the momentum spectra for the backward going neutrons. The spectra have the same universal shape observed in the inclusive reactions. We speculate that the enhanced backward neutron emission in this semi-inclusive region could be an indication for a strong dependence of the cross section on the squared total center-of-mass energy (s) and for the importance of short-range nucleon-nucleon correlations.

  9. Theoretical model analysis of (d ,x n ) reactions on 9Be and 12C at incident energies up to 50 MeV

    Science.gov (United States)

    Nakayama, Shinsuke; Kouno, Hiroshi; Watanabe, Yukinobu; Iwamoto, Osamu; Ogata, Kazuyuki

    2016-07-01

    Background: In the design of deuteron accelerator neutron sources, accurate nuclear data of deuteron-induced reactions are indispensable over a wide range of incident energy. Reliable model calculations play an important role in completing the necessary nuclear data since currently available experimental data are insufficient. We have been developing a code system dedicated for the deuteron-induced reactions, called deuteron-induced reaction analysis code system (DEURACS). It was applied successfully to (d ,x p ) reactions at 56 and 100 MeV. Purpose: The purpose of the present work is to investigate the applicability of DEURACS to (d ,x n ) reactions on 9Be and 12C for incident energies below 50 MeV and to clarify neutron production mechanism. Methods: Double-differential thick target neutron yields (TTNYs) from deuteron bombardment on thick Be and C targets are analyzed. The TTNYs are derived using the double differential (d ,x n ) cross sections calculated by DEURACS and the stopping power of deuteron in the target. The calculated TTNYs are decomposed into individual components corresponding to elastic breakup, proton stripping, and statistical decay reactions. Results: The calculated TTNYs reproduced the experimental data quantitatively well in the incident energy range up to 50 MeV. From the analysis, it was found that the proton stripping reaction makes the most dominant contribution to neutron production. Conclusions: DEURACS is applicable to (d ,x n ) reactions on 9Be and 12C for incident energies below 50 MeV. Modeling of the stripping reaction is essential to predict neutron production yields accurately in the design of deuteron accelerator neutron sources.

  10. Phosphorus/sulfur Co-doped porous carbon with enhanced specific capacitance for supercapacitor and improved catalytic activity for oxygen reduction reaction

    Science.gov (United States)

    Zhou, Yao; Ma, Ruguang; Candelaria, Stephanie L.; Wang, Jiacheng; Liu, Qian; Uchaker, Evan; Li, Pengxi; Chen, Yongfang; Cao, Guozhong

    2016-05-01

    Phosphorus (P)/sulfur (S) co-doped porous carbon derived from resorcinol and furaldehyde are synthesized through one-step sol-gel processing with the addition of phosphorus pentasulfide as P and S source followed with freeze-drying and pyrolysis in nitrogen. The P/S co-doping strategy facilitates the pore size widening both in micropore and mesopore regions, together with the positive effect on the degree of graphitization of porous carbon through elimination of amorphous carbon through the formation and evaporation of carbon disulfide. As an electrode for supercapacitor application, P/S co-doped porous carbon demonstrates 43.5% improvement on specific capacitance of the single electrode compared to pristine porous carbon in organic electrolyte at a current of 0.5 mA due to the P-induced pseudocapacitive reactions. As for electrocatalytic use, promoted electrocatalytic activity and high resistance to crossover effects of oxygen reduction reaction (ORR) in alkaline media are observed after the introduction of P and S into porous carbon. After air activation, the specific capacitance of the single electrode of sample PS-pC reaches up to 103.5 F g-1 and an improved oxygen reduction current density.

  11. Dissolution of CO2 in Brines and Mineral Reactions during Geological Carbon Storage: AN Eor Experiment

    Science.gov (United States)

    Bickle, M. J.; Chapman, H.; Galy, A.; Kampman, N.; Dubacq, B.; Ballentine, C. J.; Zhou, Z.

    2015-12-01

    Dissolution of CO2 in formation brines is likely to be a major process which stabilises stored CO2 on longer time scales and mitigates CO2 migrating through storage complexes. However very little is known about the likely rates of CO2 dissolution as CO2 flows through natural heterogeneous brine filled reservoirs. Here we report the results of sampling fluids over 6 months after a phase of CO2 injection commenced for enhanced oil recovery coupled with injection of isotopically enriched 3He and 129Xe. Modelling of the changes in fluid chemistry has previously been interpreted to indicate significant dissolution of silicate minerals where fluids remained close to saturation with calcite. These calculations, which are based on modal decomposition of changes in cation concentrations, are supported by changes in the isotopic compositions of Sr, Li and Mg. Analysis of Sr-isotopic compositions of samples from outcrops of the Frontier Formation, which forms the reservoir sampled by the EOR experiment, reveals substantial heterogeneity. Silicate mineral compositions have 87Sr/86Sr ratios between 0.709 and 0.719 whereas carbonate cements have values around 0.7076. Calculation of CO2 dissolution based on simplified 2-D flow models shows that fluids likely sample reservoir heterogeneities present on a finer scale with CO2 fingers occupying the most permeable horizons and most water flow in the adjacent slightly less permeable zones. Smaller time scale variations in 87Sr/86Sr ratios are interpreted to reflect variations in flow paths on small length scales driven by invading CO2.

  12. Effect of carbon content on carbide morphology and mechanical properties of A.R. white cast iron with 10-12% tungsten

    Energy Technology Data Exchange (ETDEWEB)

    Heydari, D. [Department of Materials Science and Engineering, Sharif University of Technology, Tehran (Iran, Islamic Republic of); Skandani, A. Alipour [Department of Engineering Science and Mechanics, Virginia Tech, Blacksburg, VA 24061 (United States); Al Haik, M., E-mail: alhaik@vt.edu [Department of Engineering Science and Mechanics, Virginia Tech, Blacksburg, VA 24061 (United States)

    2012-04-30

    Highlights: Black-Right-Pointing-Pointer Effect of W and C variation in A.R. white cast iron was studied up to 12 wt% W. It never exceeded 10 wt% in previous investigations. Black-Right-Pointing-Pointer Carbide morphologies with 2.2-3.2 wt% carbon shows that W has dominating effect on carbide morphology. Black-Right-Pointing-Pointer New carbide microstructures (GA and IA) appear in some range of carbon and its volume fraction is function of carbon content. Black-Right-Pointing-Pointer After heat treatment, new carbide morphology turns to continuous chromium carbide. Black-Right-Pointing-Pointer Wear resistance and hardness of the new alloys depends on both IA appearance presence and tungsten carbide precipitation. - Abstract: Carbide morphologies of white cast iron containing 22% Cr and 10-12% tungsten with different carbon contents (2.34-3.20 wt.%) were investigated. Results indicated that for the as-cast alloys with no heat treatments, the addition of carbon changes the morphology of carbides during air-cooling in the presence of tungsten. Light microscopy analysis revealed that for an alloy with 2.3 wt% carbon, chromium carbides possess coarse gray appearance (GA). Increasing the carbon content reduced the coarse GA zones volume fraction while a finer GA zones emerged. The coexistence of coarse and fine GA phases came to an end at 2.8 wt% carbon, at which only fine GA zones spread throughout the chromium carbide phase. Scaling up the carbon content to 3.2 wt% led to the formation of tungsten carbide and austenite in a eutectic reaction. Both fine and coarse GA zones vanished while the tungsten carbides acquired fishbone-like morphology. Upon heat treatment, the coarse GA zones vanished completely and turned into island appearance (IA) of chromium carbide. On the contrary, the finer GA zones remained unchanged after heat treatment and they coexisted with the IA. After heat treatment, the fishbone morphology shattered apart, however, the hyper chromium carbides

  13. Suzuki-Miyaura, Mizoroki-Heck carbon-carbon coupling and hydrogenation reactions catalysed by PdII and RhI complexes containing cyclodiphosphazane cis-{tBuNP(OC6H4OMe-)}2

    Indian Academy of Sciences (India)

    Sasmita Mohanty; Maravanji S Balakrishna

    2010-03-01

    The catalytic activity of the palladium complex cis-[PdCl2{(tBuNP(OC6H4OMe-))2- }2] (2) containing cis-{tBuNP(OC6H4OMe-)}2 (1) in Suzuki-Miyaura and Mizoroki-Heck carbon-carbon cross coupling reactions is described. The compound 2 also displays very high activity in Mizoroki-Heck coupling reactions. The rhodium(I) complex [RhCl(COD){(tBuNP(OC6H4OMe-))2- }] (3) acts as an excellent catalyst for the hydrogenation of several terminal olefins.

  14. Electrodeposition of Nickel onto 12K Carbon Fibre Tow in a Continuous Manner

    OpenAIRE

    Pierozynski, Boguslaw

    2012-01-01

    Nickel-coated carbon fibre (NiCCF) is an important composite material, which finds nu- merous engineering applications, primarily within: computer, telecommunication, automotive and military industries. In general, NiCCF can be produced by one of the three methods, namely: chemical vapour deposition (CVD), electroless, and electrochemical (galvanic) deposition of Ni on a carbon fibre tow material. The present paper reports a study of the process of nickel electrodeposition (at ultrathin layer...

  15. Reaction cross sections for protons on {sup 12}C, {sup 40}Ca, {sup 90}Zr and {sup 208}Pb at energies between 80 and 180 MeV

    Energy Technology Data Exchange (ETDEWEB)

    Auce, A.; Ingemarsson, A.; Johansson, R. [and others

    2005-04-01

    Results of reaction cross section measurements on {sup 12}C, {sup 40}Ca, {sup 90}Zr and {sup 208}Pb at incident proton energies between 80 and 180 MeV and for {sup 58}Ni at 81 MeV are presented. The experimental procedure is described and the results are compared with earlier measurements and predictions using macroscopic and microscopic models.

  16. Broad structures in γ-ray multiplicity gated p and α spectra in low energy 12C+93Nb and 16O+89Y reactions

    Directory of Open Access Journals (Sweden)

    Nanal V.

    2010-03-01

    Full Text Available Gamma ray multiplicity gated proton spectra have been measured in the reactions 12C+93Nb at E(12C= 40 and 45.5 MeV and 16O+89Y at E(16O= 51 and 54 MeV populating the CN 105 Ag at EX between 35 and 40 MeV. Broad structures are seen in all spectra at high gamma ray multiplicities. The present data, along with those from our earlier work on the former reaction at E(12C= 42.5 MeV, establish the compound nuclear origin of the structures. The data can be explained by incorporating a localised enhancement of nuclear level density in the excitation energy and angular momentum space. Multiplicity gated Îś spectra have also been measured in the same reaction at E(12C= 37.5 – 45 MeV. Broad structures seen in these spectra seem to have contribution from other reaction mechanisms also.

  17. FY12 ARRA-NRAP Report – Studies to Support Risk Assessment of Geologic Carbon Sequestration

    Energy Technology Data Exchange (ETDEWEB)

    Cantrell, Kirk J.; Shao, Hongbo; Thompson, C. J.; Zhong, Lirong; Jung, Hun Bok; Um, Wooyong

    2011-09-27

    This report summarizes results of research conducted during FY2012 to support the assessment of environmental risks associated with geologic carbon dioxide (CO2) sequestration and storage. Several research focus areas are ongoing as part of this project. This includes the quantification of the leachability of metals and organic compounds from representative CO2 storage reservoir and caprock materials, the fate of metals and organic compounds after release, and the development of a method to measure pH in situ under supercritical CO2 (scCO2) conditions. Metal leachability experiments were completed on 6 different rock samples in brine in equilibrium with scCO2 at representative geologic reservoir conditions. In general, the leaching of RCRA metals and other metals of concern was found to be limited and not likely to be a significant issue (at least, for the rocks tested). Metals leaching experiments were also completed on 1 rock sample with scCO2 containing oxygen at concentrations of 0, 1, 5, and 10% to simulate injection of CO2 originating from the oxy-fuel combustion process. Significant differences in the leaching behavior of certain metals were observed when oxygen is present in the CO2. These differences resulted from oxidation of sulfides, release of sulfate, ferric iron and other metals, and subsequent precipitation of iron oxides and some sulfates such as barite. Experiments to evaluate the potential for mobilization of organic compounds from representative reservoir materials and cap rock and their fate in porous media (quartz sand) have been conducted. Results with Fruitland coal and Gothic shale indicate that lighter organic compounds were more susceptible to mobilization by scCO2 compared to heavier compounds. Alkanes demonstrated very low extractability by scCO2. No significant differences were observed between the extractability of organic compounds by dry or water saturated scCO2. Reaction equilibrium appears to have been reached by 96 hours. When

  18. New measurement of cross section of evaporation residues from $^{\\textrm{nat}}$Pr+$^{12}$C reaction: A comparative study on the production of $^{149}$Tb

    CERN Document Server

    Maiti, Moumita

    2011-01-01

    Production cross sections of evaporation residues, $^{149}$Tb, $^{150}$Tb, $^{151}$Tb and $^{149}$Gd, have been measured using the stacked foil technique followed by off-line $\\gamma$-spectrometry in $^{12}$C induced reactions on naturally abundant mononuclidic praseodymium target in the 44-79 MeV incident energy range. Measured data have been interpreted comparing with previous measurements and theoretical prediction of nuclear reaction model code \\textsc{PACE4}. About 5% and 14% of the theoretical cross sections have been measured for $^{149}$Tb and $^{150}$Tb, respectively. The new cross sections of $^{149}$Tb complement those measured earlier by $\\alpha$-spectrometry. Cross sections of $^{151}$Tb are comparable to the theory. Cumulative cross section of $^{149}$Gd sheds light on the nuclear reaction mechanism. In addition, a discussion has been made to show the feasibility of producing $^{149}$Tb in $p$- and $\\alpha$-induced reactions on gadolinium isotopes.

  19. CCSD(T)-F12a study of reactions of interstellar anions C2nH-(n = 2-4) with HCCH.

    Science.gov (United States)

    Botschwina, Peter; Oswald, Rainer

    2010-04-15

    Explicitly correlated coupled cluster theory at the CCSD(T)-F12a level (Adler, T. B.; Knizia, G.; Werner, H.-J. J. Chem. Phys. 2007, 127, 221106) was employed to study the energetics of reactions of interstellar anions C(2n)H(-) with HCCH, which may formally be regarded as proton-transfer reactions. The gas-phase acidities at 0 K for the polyynes HC(2n)H with n = 2-4 are predicted to be 1516.5, 1483.2, and 1462.6 kJ mol(-1). The energy profiles of the collinear reactions are characterized by absolute minima corresponding to the hydrogen-bonded species HC(2n)(-)...HCCH, saddle points at which the proton is shared between the two anion moieties, and a second minimum in the exit channel of the reaction, which becomes less pronounced with increasing n. PMID:20088556

  20. Effect of UV and electrochemical surface treatments on the adsorption and reaction of linear alcohols on non-porous carbon fibre

    Science.gov (United States)

    Osbeck, S.; Ward, S.; Idriss, H.

    2013-04-01

    The adsorption properties of untreated, electrochemically treated and ultra-violet/ozone treated polyacrylonitrile based carbon fibres were investigated using temperature programmed desorption (TPD) on a series of linear alcohols as probes in order to understand its surface properties. Surface uptake was found to be sensitive to both the surface treatment and the nature of the adsorbates. Surface coverage increased with increasing alcohol chain due to the increase in their polarizability. It also increased with the level of surface oxygen of the fibres most likely because it facilitates the Osbnd H bond dissociation of the alcohol functional group. In addition, the desorption temperature (during TPD) tracked the surface oxygen levels (as determined from XPS O1s signal) suggesting increasing in the adsorption energy. The reactions of C1-C4 linear alcohols were also investigated on the surface of the fibre carbon. The main reaction was dehydrogenation to the corresponding aldehydes; the dehydration reaction to olefins was not observed. The dehydrogenation reaction was sensitive to the length of the alky chain. It was highest for methanol (to formaldehyde) and decreased with increasing the carbon number. Overall TPD of linear alcohols was shown to be a promising method for quantifying the level and strength of bonding occurring on carbon fibre surfaces.

  1. Reaction of carbon tetrachloride with methane in a non-equilibrium plasma at atmospheric pressure, and characterisation of the polymer thus formed

    Energy Technology Data Exchange (ETDEWEB)

    Gaikwad, Vaibhav [Process Safety and Environment Protection Research Group, School of Engineering, The University of Newcastle, Callaghan, NSW 2308 (Australia); Kennedy, Eric, E-mail: Eric.Kennedy@newcastle.edu.au [Process Safety and Environment Protection Research Group, School of Engineering, The University of Newcastle, Callaghan, NSW 2308 (Australia); Mackie, John [Process Safety and Environment Protection Research Group, School of Engineering, The University of Newcastle, Callaghan, NSW 2308 (Australia); Holdsworth, Clovia [Centre for Organic Electronics, Chemistry Building, School of Environmental and Life Sciences, University of Newcastle, Callaghan, NSW 2308 (Australia); Molloy, Scott; Kundu, Sazal; Stockenhuber, Michael [Process Safety and Environment Protection Research Group, School of Engineering, The University of Newcastle, Callaghan, NSW 2308 (Australia); Dlugogorski, Bogdan [School of Engineering and Information Technology, Murdoch University, Murdoch, WA 6150 (Australia)

    2014-09-15

    Highlights: • CCl{sub 4} remediation using non-equilibrium plasma and non-oxidative conditions is proposed. • The reaction mechanism relies on experimental data and quantum chemical analysis. • Comprehensive mass balance for the reaction is provided. • CCl{sub 4} is converted to an environmentally benign and potentially useful polymer. • Characterisation of the polymer structure based on NMR and FTIR analyses is presented. - Abstract: In this paper we focus on the development of a methodology for treatment of carbon tetrachloride utilising a non-equilibrium plasma operating at atmospheric pressure, which is not singularly aimed at destroying carbon tetrachloride but rather at converting it to a non-hazardous, potentially valuable commodity. This method encompasses the reaction of carbon tetrachloride and methane, with argon as a carrier gas, in a quartz dielectric barrier discharge reactor. The reaction is performed under non-oxidative conditions. Possible pathways for formation of major products based on experimental results and supported by quantum chemical calculations are outlined in the paper. We elucidate important parameters such as carbon tetrachloride conversion, product distribution, mass balance and characterise the chlorinated polymer formed in the process.

  2. Single-walled carbon nanotubes as nano-electrode and nano-reactor to control the pathways of a redox reaction.

    Science.gov (United States)

    McSweeney, Robert L; Chamberlain, Thomas W; Davies, E Stephen; Khlobystov, Andrei N

    2014-11-28

    Single-walled carbon nanotubes have been demonstrated as effective nanoscale containers for a redox active organometallic complex Cp(Me)Mn(CO)3, acting simultaneously as nano-electrode and nano-reactor. Extreme spatial confinement of the redox reaction within the nanotubes changes its pathway compared to bulk solution due to stabilisation of a reactive intermediate.

  3. Enhanced polysulphide redox reaction using a RuO2 nanoparticle-decorated mesoporous carbon as functional separator coating for advanced lithium-sulphur batteries.

    Science.gov (United States)

    Balach, J; Jaumann, T; Mühlenhoff, S; Eckert, J; Giebeler, L

    2016-06-21

    A multi-functional RuO2 nanoparticle-embedded mesoporous carbon-coated separator is used as an electrocatalytic and adsorbing polysulphide-net to enhance the redox reaction of migrating polysulphides, to improve active material utilization and boost the electrochemical performance of lithium-sulphur batteries. PMID:27270267

  4. Developments in Analytical Chemistry: Acoustically Levitated Drop Reactors for Enzyme Reaction Kinetics and Single-Walled Carbon Nanotube-Based Sensors for Detection of Toxic Organic Phosphonates

    Science.gov (United States)

    Field, Christopher Ryan

    2009-01-01

    Developments in analytical chemistry were made using acoustically levitated small volumes of liquid to study enzyme reaction kinetics and by detecting volatile organic compounds in the gas phase using single-walled carbon nanotubes. Experience gained in engineering, electronics, automation, and software development from the design and…

  5. Mechanistic studies of the copolymerization reaction of oxetane and carbon dioxide to provide aliphatic polycarbonates catalyzed by (Salen)CrX complexes.

    Science.gov (United States)

    Darensbourg, Donald J; Moncada, Adriana I; Choi, Wonsook; Reibenspies, Joseph H

    2008-05-21

    Chromium salen derivatives in the presence of anionic initiators have been shown to be very effective catalytic systems for the selective coupling of oxetane and carbon dioxide to provide the corresponding polycarbonate with a minimal amount of ether linkages. Optimization of the chromium(III) system was achieved utilizing a salen ligand with tert-butyl groups in the 3,5-positions of the phenolate rings and a cyclohexylene backbone for the diimine along with an azide ion initiator. The mechanism for the coupling reaction of oxetane and carbon dioxide has been studied. Based on binding studies done by infrared spectroscopy, X-ray crystallography, kinetic data, end group analysis done by (1)H NMR, and infrared spectroscopy, a mechanism of the copolymerization reaction is proposed. The formation of the copolymer is shown to proceed in part by way of the intermediacy of trimethylene carbonate, which was observed as a minor product of the coupling reaction, and by the direct enchainment of oxetane and CO 2. The parity of the determined free energies of activation for these two processes, namely 101.9 kJ x mol (-1) for ring-opening polymerization of trimethylene carbonate and 107.6 kJ x mol (-1) for copolymerization of oxetane and carbon dioxide supports this conclusion.

  6. A Novel One-Pot and One-Step Microwave-Assisted Cyclization-Methylation Reaction of Amino Alcohols and Acetylated Derivatives with Dimethyl Carbonate and TBAC

    Science.gov (United States)

    Ochoa-Terán, Adrián; Guerrero, Leticia; Rivero, Ignacio A.

    2014-01-01

    A simple and efficient microwave-assisted methodology for the synthesis of 4-substituted-3-methyl-1,3-oxazolidin-2-ones from amino alcohols catalyzed by a ionic liquid was developed. This novel one-pot and one-step cyclization-methylation reaction represents an easier and faster method than any other reported protocols that can be used to obtain the desired products in good yields and high purity. Applying microwave irradiation at 130°C in the presence of TBAC, dimethyl carbonate acts simultaneously as carbonylating and methylating agent and surprisingly promotes an in situ basic trans esterification when a N-acetylated amino alcohol is used as starting material. Furthermore, dimethyl carbonate worked better than diethyl carbonate in performing this reaction. PMID:25692177

  7. A novel one-pot and one-step microwave-assisted cyclization-methylation reaction of amino alcohols and acetylated derivatives with dimethyl carbonate and TBAC.

    Science.gov (United States)

    Ochoa-Terán, Adrián; Guerrero, Leticia; Rivero, Ignacio A

    2014-01-01

    A simple and efficient microwave-assisted methodology for the synthesis of 4-substituted-3-methyl-1,3-oxazolidin-2-ones from amino alcohols catalyzed by a ionic liquid was developed. This novel one-pot and one-step cyclization-methylation reaction represents an easier and faster method than any other reported protocols that can be used to obtain the desired products in good yields and high purity. Applying microwave irradiation at 130°C in the presence of TBAC, dimethyl carbonate acts simultaneously as carbonylating and methylating agent and surprisingly promotes an in situ basic trans esterification when a N-acetylated amino alcohol is used as starting material. Furthermore, dimethyl carbonate worked better than diethyl carbonate in performing this reaction. PMID:25692177

  8. A Novel One-Pot and One-Step Microwave-Assisted Cyclization-Methylation Reaction of Amino Alcohols and Acetylated Derivatives with Dimethyl Carbonate and TBAC

    Directory of Open Access Journals (Sweden)

    Adrián Ochoa-Terán

    2014-01-01

    Full Text Available A simple and efficient microwave-assisted methodology for the synthesis of 4-substituted-3-methyl-1,3-oxazolidin-2-ones from amino alcohols catalyzed by a ionic liquid was developed. This novel one-pot and one-step cyclization-methylation reaction represents an easier and faster method than any other reported protocols that can be used to obtain the desired products in good yields and high purity. Applying microwave irradiation at 130°C in the presence of TBAC, dimethyl carbonate acts simultaneously as carbonylating and methylating agent and surprisingly promotes an in situ basic trans esterification when a N-acetylated amino alcohol is used as starting material. Furthermore, dimethyl carbonate worked better than diethyl carbonate in performing this reaction.

  9. Electrocatalytical study of carbon supported Pt, Ru and bimetallic Pt–Ru nanoparticles for oxygen reduction reaction in alkaline media

    Energy Technology Data Exchange (ETDEWEB)

    Hosseini, M.G., E-mail: mg-hosseini@tabrizu.ac.ir; Zardari, P.

    2015-08-01

    Highlights: • Binary catalyst Pt.Ru/C is evaluated towards ORR. • Pt.Ru/C nanoparticles revealed best ORR catalytical activity. • The 120 mV/dec Tafel slope indicated that the first electron transfer is the rds. • The active number sites of Pt.Ru/C catalyst were 3 times higher than Pt/C. - Abstract: Carbon supported Pt, Ru and bimetallic Pt–Ru nanoparticles (Pt/C, Ru/C and Pt.Ru/C) have been prepared by the chemical reduction method. Particle morphology, composition and structure of nanoparticles have been investigated by scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) analysis. SEM results showed a uniform dispersion of nanoparticles with rough and porous structure into carbon supports with the average particle size of 30–64 nm. EDX analysis demonstrated the presence of both Pt and Ru nanoparticles in each gas diffusion electrode. The Pt/C, Ru/C and Pt.Ru/C composites were used as electrocatalyst for oxygen reduction reaction (ORR) in alkaline media. The ORR activities of cathodes were characterized using cyclic voltammetry (CV), polarization technique, AC impedance spectroscopy (EIS) and chronoamperometry. CV and polarization curves showed significantly higher activity on Pt.Ru/C electrocatalyst than observed on Pt/C and Ru/C catalysts, which can be related to synergistic effect, which is playing a critical role in ORR activity. The Tafel slope values of 120 mV/dec showed that the first electron transfer is the rate determining step. The EIS results of cathodes under different polarization potentials indicated two different behaviours which depend on the applied dc potentials and reveal different electrochemical processes occurring on the electrodes.

  10. Lignin-derived electrospun carbon nanofiber mats with supercritically deposited Ag nanoparticles for oxygen reduction reaction in alkaline fuel cells

    International Nuclear Information System (INIS)

    Highlights: • Electrospun carbon nanofiber mats were prepared from a natural product of lignin. • The freestanding mats were flexible with BET specific surface area of ∼583 m2/g. • The mats were surface-deposited with Ag nanoparticles via the scCO2 method. • Novel electrocatalytic systems of Ag/ECNFs exhibited high activities towards ORR. - Abstract: Ag nanoparticles (AgNPs) (11, 15, and 25 wt.%) were deposited on the surface of the freestanding and mechanically flexible mats consisting of lignin-derived electrospun carbon nanofibers (ECNFs) by the supercritical CO2 method followed by the thermal treated at 180 °C. The electrochemical activity of Ag/ECNFs electrocatalyst systems towards oxygen reduction reaction (ORR) was studied in 0.1 M KOH aqueous solution using the rotating disk/rotating ring disk electrode (RDE/RRDE) technique. The SEM, TEM, and XRD results indicated that, the spherical AgNPs were uniformly distributed on the ECNF surface with sizes in the range of 2-10 nm. The electrocatalytic results revealed that, all of the Ag/ECNFs systems exhibited high activity in ORR and demonstrated close-to-theoretical four-electron pathway. In particular, the mass activity of 15 wt.% Ag/ECNFs system was the highest (119 mA mg−1), exceeding that of HiSPEC 4100™ commercial Pt/C catalyst (98 mA mg−1). This study suggested that the lignin-derived ECNF mats surface-deposited with AgNPs would be promising as cost-effective and highly efficient electrocatalyst for ORR in alkaline fuel cells

  11. [Reaction of 3-aryl-2-nitroacrylates with titanium tetrachloride. Formation of 4H-1,2-oxazines and hydroxy-arylaldehydes].

    Science.gov (United States)

    Hirotani, S; Zen, S

    1994-04-01

    The reaction of ethyl 3-aryl-2-nitroacrylate (1a: aryl = 3-methoxyphenyl) with toluene in the presence of titanium tetrachloride gave 4-(4'-methyl-phenyl)-4H-1,2-benzoxazine (3) in a 44.2% yield. The acrylate 1a reacted with dichloromethane in the presence of titanium tetrachloride to give 5-methoxy-salicylaldehyde (2a) in a 61.8% yield. Therefore, 2a was presumed to be formed via an intermediate 4H-1,2-benzoxazine (3'), followed by ring opening to quinone methide and cyano formate. In a similar reaction using both toluene and dichloromethane, 1 bearing a 2-naphthyl group gave a dimer of quinone methide and 1-hydroxy-2-naphthaldehyde via 4H-naphth[2,1-e]-1,2-oxazine, respectively.

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

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Nano-sized Li4Ti5O12 has been prepared through solid state reaction by using axiolitic TiO2 as precursor. • The prepared nano-sized Li4Ti5O12 anode material shows excellent electrochemical performance. • The utilization of precursor with special morphology and size is one of the useful ways to prepare more active electrode materials. - Abstract: Spinel nano-sized Li4Ti5O12 anode material of secondary lithium-ion battery has been successfully prepared by solid state reaction using axiolitic TiO2 assembled by 10–20 nm nanoparticles and Li2CO3 as precursors. The synthesis condition, grain size effect and corresponding electrochemical performance of the special Li4Ti5O12 have been studied in comparison with those of the normal Li4Ti5O12 originated from commercial TiO2. We also propose the mechanism that using the nano-scaled TiO2 with special structure and unexcess Li2CO3 as precursors can synthesize pure phase nano-sized Li4Ti5O12 at 800 °C through solid state reaction. The prepared nano-sized Li4Ti5O12 anode material for Li-ion batteries shows excellent capacity performance with rate capacity of 174.2, 164.0, 157.4, 146.4 and 129.6 mA h g−1 at 0.5, 1, 2, 5 and 10 C, respectively, and capacity retention of 95.1% after 100 cycles at 1 C. In addition, the specific capacity fade for the cell with the different Li4Ti5O12 active materials resulted from the increase of internal resistance after 100 cycles is compared

  13. DFT investigations of the reaction mechanism of diethyl carbonate synthesis catalyzed by Cu(I)/β or Pd(II)/β zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Yongli [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Wang, Shengping, E-mail: spwang@tju.edu.cn [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Huang, Shouying [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Li, Zhong [Key Laboratory of Coal Science and Technology of Ministry of Education, Taiyuan University of Technology, Taiyuan 030024, Shanxi (China); Ma, Xinbin [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China)

    2014-07-01

    Density functional theory (DFT) calculations are used to investigate the oxidative carbonylation of ethanol occurring on Cu(I)/β or Pd(II)/β. The thermochemistry and activation energy for all elementary steps involved in the formation of diethyl carbonate are presented. Upon calculation, we identify that the mechanisms for the formation of surface O atom are varying on different catalysts. Ethanol can react with the surface O atom to produce (C{sub 2}H{sub 5}O)(OH)-M/β (M = Cu{sup +}, Pd{sup 2+}) species. And this intermediate can further react with carbon monoxide or ethanol to give monoethyl carbonate or di-ethoxied species ((C{sub 2}H{sub 5}O){sub 2}-M/β). Diethyl carbonate can form via two distinct reaction pathways: (I) ethanol reacts with monoethyl carbonate or (II) carbon monoxide inserts into di-ethoxide species. Upon calculation, we confirmed that both reaction pathways for the formation of DEC are accessible on Cu(I)/β catalyst, whereas only Path II is achievable on Pd(II)/β catalyst.

  14. Search for a three-particle component of the Esub(CM) = 11. 1 MeV 5/sup -/ resonance in the /sup 12/C + /sup 16/O reaction

    Energy Technology Data Exchange (ETDEWEB)

    Gersch, H.U.; Schobbert, H.; Wohlfarth, D. (Zentralinstitut fuer Kernforschung, Rossendorf bei Dresden (German Democratic Republic))

    1983-08-01

    The 11.1 MeV 5/sup -/ resonance in the /sup 12/C + /sup 16/O reaction is remeasured and the position of the resonance is determined to be Esub(x)(/sup 28/Si) = (27.881 +- 0.022)MeV. A kinematically complete study of the /sup 12/C(/sup 16/O, ..cap alpha../sup 12/C)/sup 12/C reaction into this resonance is carried out. Particle identification is based on the reaction kinematics. No evidence for a /sup 12/C-..cap alpha..-/sup 12/C component of this resonance is found.

  15. Processing and characterization of a carbon black-filled electrically conductive Nylon-12 nanocomposite produced by selective laser sintering

    International Nuclear Information System (INIS)

    Selective laser sintering (SLS), a layered manufacturing technique was explored to process an electrically conductive polymer nanocomposite made of Nylon-12 reinforced with 4 wt% of carbon black. SLS process parameters were optimized in order to maximize the flexural modulus. The porosity and morphology were studied using optical microscopy and scanning electron microscopy (SEM). The crystalline state was characterized using differential scanning calorimetry (DSC) and X-ray diffraction (XRD). The electrical conductivity was determined using the four probe technique. Results indicate that carbon black-filled Nylon-12 nanocomposites can be successfully made by SLS. Maximum flexural modulus values of 1750 MPa and 1450 MPa were achieved for the neat polymer and the nanocomposite, respectively. A reduction in the flexural modulus of the nanocomposite is likely due to the formation of a segregated structure in the nanocomposite and a weak polymer-filler interface. The optimized neat polymer and the nanocomposites had average densities of around 97% and 96% relative to full density, respectively. The electrical conductivity of the nanocomposite was approximately 1 x 10-4 S/cm, which is five orders of magnitude higher than that of the neat polymer processed by SLS, and indicates that the onset of percolation behavior occurs below the 4 wt% loading of carbon black.

  16. Subnanometer Molybdenum Sulfide on Carbon Nanotubes as a Highly Active and Stable Electrocatalyst for Hydrogen Evolution Reaction.

    Science.gov (United States)

    Li, Ping; Yang, Zhi; Shen, Juanxia; Nie, Huagui; Cai, Qiran; Li, Luhua; Ge, Mengzhan; Gu, Cancan; Chen, Xi'an; Yang, Keqin; Zhang, Lijie; Chen, Ying; Huang, Shaoming

    2016-02-10

    Electrochemically splitting water for hydrogen evolution reaction (HER) has been viewed as a promising approach to produce renewable and clean hydrogen energy. However, searching for cheap and efficient HER electrocatalysts to replace the currently used Pt-based catalysts remains an urgent task. Herein, we develop a one-step carbon nanotube (CNT) assisted synthesis strategy with CNTs' strong adsorbability to mediate the growth of subnanometer-sized MoS(x) on CNTs. The subnanometer MoS(x)-CNT hybrids achieve a low overpotential of 106 mV at 10 mA cm(-2), a small Tafel slope of 37 mV per decade, and an unprecedentedly high turnover frequency value of 18.84 s(-1) at η = 200 mV among all reported non-Pt catalysts in acidic conditions. The superior performance of the hybrid catalysts benefits from the presence of a higher number of active sites and the abundant exposure of unsaturated S atoms rooted in the subnanometer structure, demonstrating a new class of subnanometer-scale catalysts. PMID:26765150

  17. Positive Effect of Heat Treatment on Carbon-Supported CoS Nanocatalysts for Oxygen Reduction Reaction

    Directory of Open Access Journals (Sweden)

    Haihong Zhong

    2015-07-01

    Full Text Available It is of increasing interest and an important challenge to develop highly efficient less-expensive cathode catalysts for anion-exchange membrane fuel cells (AEMFCs. In this work, we have directly prepared a carbon-supported CoS nanocatalyst in a solvothermal route and investigated the effect of heat-treatment on electrocatalytic activity and long-term stability using rotating ring-disk electrode (RRDE. The results show that the heat-treatment below 400 °C under nitrogen atmosphere significantly enhanced the electrocatalytic performance of CoS catalyst as a function of annealed temperature in terms of the cathodic current density, the half-wave potential, the HO2− product and the number of electrons transferred. The CoS catalyst that annealed at 400 °C (CoS-400 has exhibited a promising performance with the half-wave potential of 0.71 V vs. RHE (the highest one for non-precious metal chalcogenides, the minimum HO2− product of 4.3% at 0.60 V vs. RHE and close to the 4-electron pathway during the oxygen reduction reaction in 0.1 M KOH. Also, the CoS-400 catalyst has comparable durability to the Pt/C catalyst.

  18. Heavy fragment energies and angular distributions in the reaction of 85 MeV/nucleon 12C with medium-A target

    International Nuclear Information System (INIS)

    Using the thin target - thin catchers techniques, masses, mean recoil energies and angular distributions of target residues have been measured for 86 MeV/nucleon 12C induced reactions. Several different nuclear reaction processes, from peripheral to central collisions have been observed. Experimental results are partly reproduced by intra-nuclear cascade + evaporation calculations. Up to now, the production of the lightest masses (44< A<71) recoiling with high kinetic energies is not correctly understood by theoretical models. More exclusive experiments are needful to check if the formation of a highly excited quasi-compound nucleus could be a possible explanation of the phenomena

  19. Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction

    KAUST Repository

    Chua, Ming Hui

    2015-08-17

    The straightforward synthesis of 3,5-di(triphenylethylenyl) BODIPYs 1–3 from the condensation of 2-(triphenylethylenyl) pyrrole with aryl aldehydes are surprisingly found to produce side products that are hydrogenated at one of the two triphenylethylene substituents. It was also observed that the subsequent Scholl type reaction of 1 resulted in a “1,2-migratory shift” of one triphenylethylene substituent in addition to a ring closing reaction. Preliminary investigations, including DFT calculations and isolation of intermediates, were conducted to study these unusual observations on BODIPY chemistry.

  20. Two-neutron transfer reaction mechanisms in $^{12}$C($^6$He,$^{4}$He)$^{14}$C using a realistic three-body $^{6}$He model

    OpenAIRE

    Smalley, D.; F. Sarazin; Nunes, F. M.; Brown, B. A.; Adsley, P.; Al-Falou, H; Andreoiu, C.; Baartman, B.; Ball, G. C.; Blackmon, J. C.; Boston, H. C.; Catford, W. N.; Chagnon-Lessard, S.; Chester, A.; Churchman, R. M.

    2013-01-01

    The reaction mechanisms of the two-neutron transfer reaction $^{12}$C($^6$He,$^4$He) have been studied at 30 MeV at the TRIUMF ISAC-II facility using the SHARC charged-particle detector array. Optical potential parameters have been extracted from the analysis of the elastic scattering angular distribution. The new potential has been applied to the study of the transfer angular distribution to the 2$^+_2$ 8.32 MeV state in $^{14}$C, using a realistic 3-body $^6$He model and advanced shell mode...

  1. A kinetic study on the adsorption and reaction of hydrogen over silica-supported ruthenium and silver-ruthenium catalysts during the hydrogenation of carbon monoxide

    Energy Technology Data Exchange (ETDEWEB)

    VanderWiel, D.P.

    1999-02-12

    Although the catalytic hydrogenation of carbon monoxide has been a subject of considerable investigation for many years, its increasing economical attractiveness as an industrial source of hydrocarbons has recently led to a search for more active and selective catalysts. A fundamental problem in the development of such catalysts is an incomplete knowledge of the operative surface processes, due in large part to the inability to accurately measure surface concentrations of reactant species during reaction. Specifically, the concentration of surface hydrogen proves difficult to estimate using normally revealing techniques such as transient isotopic exchange due to kinetic isotope effects. Knowledge of such concentrations is essential to the determination of the mechanisms of adsorption and reaction, since many kinetic parameters are concentration dependent. It is the aim of this research to investigate the mechanism and kinetics of the adsorption and reaction of hydrogen on silica-supported ruthenium and silver-ruthenium catalysts during the hydrogenation of carbon monoxide. By preadsorbing carbon monoxide onto the surface of ruthenium and silver-ruthenium catalysts, the kinetics of hydrogen adsorption and reaction can be monitored upon exposure of this surface to ambient hydrogen gas. This is accomplished by conducting identical experiments on two separate systems. First, the formation of methane is monitored using mass spectroscopy, and specific reaction rates and apparent activation energies are measured. Next, in situ {sup 1}H-NMR is used to monitor the amount of hydrogen present on the catalyst surface during adsorption and reaction. The results for these two sets of experiments are then combined to show a correlation between the rate of reaction and the surface hydrogen concentration. Finally, transition state theory is applied to this system and is used to explain the observed change in the apparent activation energy. The structure sensitivity of hydrogen

  2. ATOMIC-LEVEL MODELING OF CO2 DISPOSAL AS A CARBONATE MINERAL: A SYNERGETIC APPROACH TO OPTIMIZING REACTION PROCESS DESIGN; FINAL

    International Nuclear Information System (INIS)

    Fossil fuels, especially coal, can support the energy demands of the world for centuries to come, if the environmental problems associated with CO(sub 2) emissions can be overcome. Permanent and safe methods for CO(sub 2) capture and disposal/storage need to be developed. Mineralization of stationary-source CO(sub 2) emissions as carbonates can provide such safe capture and long-term sequestration. Mg-rich lamellar hydroxide mineral carbonation is a leading process candidate, which generates the stable naturally occurring mineral magnesite (MgCO(sub 3)) and water. Key to process cost and viability are the carbonation reaction rate and its degree of completion. This process, which involves simultaneous dehydroxylation and carbonation is very promising, but far from optimized. In order to optimize the dehydroxylation/carbonation process, an atomic-level understanding of the mechanisms involved is needed. In this investigation Mg(OH)(sub 2) was selected as a model Mg-rich lamellar hydrocide carbonation feedstock material due to its chemical and structural simplicity. Since Mg(OH)(sub 2) dehydroxylation is intimately associated with the carbonation process, its mechanisms are also of direct interest in understanding and optimizing the process. The aim of the current innovative concepts project is to develop a specialized advanced computational methodology to complement the ongoing experimental inquiry of the atomic level processes involved in CO(sub 2) mineral sequestration. The ultimate goal is to integrate the insights provided by detailed predictive simulations with the data obtained from optical microscopy, FESEM, ion beam analysis, SIMS, TGA, Raman, XRD, and C and H elemental analysis. The modeling studies are specifically designed to enhance the synergism with, and complement the analysis of, existing mineral-CO(sub 2) reaction process studies being carried out under DOE UCR Grant DE-FG2698-FT40112. Direct contact between the simulations and the experimental

  3. Carbon sequestration in surface flow constructed wetland after 12 years of swine wastewater treatment

    Science.gov (United States)

    Constructed wetlands used for the treatment of swine wastewater may potentially sequester significant amounts of carbon. In past studies, we evaluated the treatment efficiency of wastewater in marsh-pond-marsh design wetland system. The functionality of this system was highly dependent on soil carbo...

  4. Distribution and persistence of probiotic Streptococcus salivarius K12 in the human oral cavity as determined by real-time quantitative polymerase chain reaction.

    Science.gov (United States)

    Horz, H-P; Meinelt, A; Houben, B; Conrads, G

    2007-04-01

    The bacteriocin producer Streptococcus salivarius K12 is used as a probiotic targeting the oral cavity, so our study aimed to assess whether its dispersal and persistence could be monitored using real-time quantitative polymerase chain reaction. To this end, we designed polymerase chain reaction primers and a hybridization probe specifically targeting salA, which encodes for the prepropeptide of salivaricin A. Using a single individual as our subject, we administered four lozenges of K12 Throat Guard per day over 3 days, then measured salA gene levels for 16 different oral sites at six different intervals over 35 days. Four samples each from gingival sulci and from teeth all remained negative. In contrast, in saliva and at all mucosal membranes K12 was detected, but with varying amounts and time profiles. Relatively high salA gene copy numbers, calibrated on the basis of colony-forming units, were seen on the tongue (maximum 4.6 x 10(4)/swab at day 4), in stimulated saliva (2.4 x 10(4)/ml, day 4) and on buccal membranes (1.3 x 10(4)/swab, day 8). K12 was present on both sides of the pharynx but asymmetrically in both quantity and duration. In conclusion, we have developed a real-time quantitative-polymerase chain reaction for counting S. salivarius K12 at various sites in the oral cavity. In the individual studied, K12 could be detected at the mucosal membranes for as long as 3 weeks, but with steadily decreasing numbers after day 8. Thus, K12 may have the potential to control oral bacterial infections only when the uptake is repeated frequently. PMID:17311636

  5. Geochemical Impacts to Groundwater from Geologic Carbon Sequestration: Controls on pH and Inorganic Carbon Concentrations from Reaction Path and Kinetic Modeling

    Science.gov (United States)

    Geologic carbon sequestration has the potential to cause long-term reductions in global emissions of carbon dioxide to the atmosphere. Safe and effective application of carbon sequestration technology requires an understanding of the potential risks to the quality of underground...

  6. Study of two- and multi-particle correlations in 12C+24Mg and 12C+208Pb reactions at E=35 AMeV

    Directory of Open Access Journals (Sweden)

    Quattrocchi L.

    2016-01-01

    Full Text Available Two and multi particle correlations from the decay of sources produced in 12C+24Mg and 12C+208Pb collisions at E=35 AMeV have been studied by using the forward part (1° < θlab < 30° of the CHIMERA multi-detector. Correlations and invariant mass spectroscopy are used to explore simultaneous and sequential decays of resonances in light isotopes with Z∼3-6, produced in peripheral collisions via the break-up of excited quasi-projectiles. Among them we mention 5Li, 6Li, 6Be, 8Be and the astrophysically important state in 12C decaying into three alpha particles. Results and future perspectives at the INFN-LNS will be presented.

  7. Mass asymmetry dependence of fusion time-scales in 11B+237Np and 12C, 16O, 19F+232Th reactions in a dynamical trajectory model

    International Nuclear Information System (INIS)

    Dynamical trajectory calculations were carried out for the reactions of 11B+237Np and 12C, 16O and 19F+232Th, having mass asymmetries on either side of the Businaro-Gallone critical mass asymmetry αBG, in order to examine the mass asymmetry dependence of fusion reactions in these systems. The compound nucleus formation times were calculated as a function of the partial wave of the reaction for all the systems. This study brings out that for systems with αBG, the formation times are significantly larger than for α>αBG, which is caused by the dynamical effects involved in the large scale shape changes taking place in the fusion process as well as due to the interplay between the thermal and the collective motion during the collision process. The calculated time scales are comparable to the experimental values derived from the pre-fission neutron multiplicity measurements. (author). 16 refs., 4 figs., 1 tab

  8. THE INFLUENCE OF THE POROUS STRUCTURE OF LOCAL ACTIVATED CARBONS ON THE IMMOBILIZATION OF THE CONGO RED DYE AND VITAMIN B 12

    Directory of Open Access Journals (Sweden)

    N. Timbaliuc

    2013-06-01

    Full Text Available The adsorption properties of activated carbons, obtained from local raw materials (nut shells, peach and plum stones, towards Congo Red and vitamin B12 have been studied. The values of adsorption of these marker-substances are in direct correlation with the structural characteristics of the studied samples of activated carbons, in particular, with their mesopore volume.

  9. The 12C(3He,pγ)14N reaction cross section for γ-ray spectroscopy simulation of fusion plasmas

    International Nuclear Information System (INIS)

    High resolution γ-ray spectroscopy measurements were performed in JET (3He)D plasmas with high energy ion populations driven by radio-frequency (RF) heating. One of the first reactions investigated was 12C(3He,pγ)14N, which was observed at low 3He concentrations. In order to interpret the measurements in this work, cross section data for the 12C(3He,pγ)14N reaction are evaluated. Available data for the population of excited states in 14N up to the eighth level are assessed in the range E3He=0-5 MeV. Discrepancies and gaps in the database have been solved by means of interpolations and consistency analysis. The evaluated cross section data are used to predict the intensity ratio of characteristic 2.31 and 1.63 MeV γ-rays.

  10. Indirect measurement of the {sup 15}N(p,{alpha}){sup 12}C reaction cross section through the Trojan-Horse Method

    Energy Technology Data Exchange (ETDEWEB)

    La Cognata, M.; Romano, S.; Spitaleri, C.; Cherubini, S.; Lamia, L.; Pizzone, R.G.; Tumino, A. [Universita di Catania, Dipartimento di Metodologie Fisiche e Chimiche per l' Ingegneria, Catania (Italy); INFN, Laboratori Nazionali del Sud, Catania (Italy); Tribble, R.; Trache, L.; Fu, Changbo; Mukhamedzhanov, A.; Tabacaru, G. [Texas A and M University, Cyclotron Institute, College Station, TX (United States); Rolfs, C. [Ruhr-Universitaet, Bochum (Germany)

    2006-03-15

    The low-energy, bare-nucleus cross section for {sup 15}N(p,{alpha}){sup 12}C is extracted by means of the Trojan-Horse Method applied to the {sup 2}H({sup 15}N,{alpha}{sup 12}C)n reaction at E{sub beam}=60 MeV. The astrophysical S-factor is compared to the direct data in the same energy region. A nice agreement shows up down to 100 keV, while the low-energy behaviour of the S-factor suggests a smaller rate than is reported in the literature. (orig.)

  11. Chemical Reaction CO+OH(•) → CO2+H(•) Autocatalyzed by Carbon Dioxide: Quantum Chemical Study of the Potential Energy Surfaces.

    Science.gov (United States)

    Masunov, Artëm E; Wait, Elizabeth; Vasu, Subith S

    2016-08-01

    The supercritical carbon dioxide medium, used to increase efficiency in oxy combustion fossil energy technology, may drastically alter both rates and mechanisms of chemical reactions. Here we investigate potential energy surface of the second most important combustion reaction with quantum chemistry methods. Two types of effects are reported: formation of the covalent intermediates and formation of van der Waals complexes by spectator CO2 molecule. While spectator molecule alter the activation barrier only slightly, the covalent bonding opens a new reaction pathway. The mechanism includes sequential covalent binding of CO2 to OH radical and CO molecule, hydrogen transfer from oxygen to carbon atoms, and CH bond dissociation. This reduces the activation barrier by 11 kcal/mol at the rate-determining step and is expected to accelerate the reaction rate. The finding of predicted catalytic effect is expected to play an important role not only in combustion but also in a broad array of chemical processes taking place in supercritical CO2 medium. It may open a new venue for controlling reaction rates for chemical manufacturing. PMID:27351778

  12. A Computational Study on the Mechanism for the K_2CO_3-catalyzed Reaction of Carbon Dioxide and 1-Chlo-2-propanol

    Institute of Scientific and Technical Information of China (English)

    张福兰; 万邦江; 黄辉胜

    2012-01-01

    The microcosmic reaction mechanism of K2CO3-catalyzed 1-chlo-2-propanol and carbon dioxide has been investigated by density functional theory(DFT) at the GGA/PW91/DNP level.We optimize the geometric configurations of reactants,intermediates,transition states,and products.The energy analysis calculation approves the authenticity of intermediates and transition states.According to our calculations,four feasible reaction pathways are found.The main pathway of the reaction is ReA → IMA1 → TSA1 → IMA2 → IMA5 → TSA5 → P.Besides,we also in-vestigate the reaction mechanism of 1-chlo-2-propanol and carbon dioxide without K2CO3-catalyzation by the same theory and level.The computational results indicate that the activation barrier with K2CO3-catalyzed is smaller than the activation barrier without K2CO3-catalyzed.That is to say,K2CO3 can promote the reaction to give the product in a high yield,which is in agreement with the experimental results.

  13. Realization of an electrostatic collection of nuclei. Application to the production of isotopes and to nuclear reactions induced by 12C beams at 86 MeV/nucleon

    International Nuclear Information System (INIS)

    The working conditions of a new on-line electrostatic collection system are presented. The main characteristics are high efficiency (reaching 20%) and short delay time (down to the millisecond). A systematic study of this method, comparing experiment and theory, is done. The device has been successfully used on the one hand for the exotic isotopes research (discovery of 184Pb) and on the other hand for the study of reactions induced by a 12C beam at 86 MeV/nucleon

  14. Polypyrrole-derived mesoporous nitrogen-doped carbons with intrinsic catalytic activity in the oxygen reduction reaction

    OpenAIRE

    Sevilla Solís, Marta; Yu, Linghui; Fellinger, Tim Patrick; Fuertes Arias, Antonio Benito; Titirici, Maria-Magdalena

    2013-01-01

    [EN] N-doped mesoporous carbons containing small amounts of graphitic carbon have been successfully prepared using the nanocasting technique. Polypyrrole was used as N-dopant carbon precursor and SBA-15 or silica xerogel as templates. Graphitic carbon domains provide a good electronic conductivity of up to 0.33 S cm−1, a necessary property for electrochemical applications, while a mesoporous structure reduces mass transport limitations. These characteristics are further combined with a high N...

  15. Co3O4 NPs Embedded in N-doped Carbon Fibers as a Bifunctional Electrocatalyst for Oxygen Reduction and Evolution Reactions

    Science.gov (United States)

    Guo, Yao-Fang; Liu, Ting; Sun, Ke-Ning

    2016-05-01

    Oxygen reduction and evolution reactions are important and major challenges to Li-air batteries. In this report, a three-dimensional (3D) bifunctional electrocatalyst was prepared by embedding Co3O4 nanoparticles into nitrogen-doped carbon nanofibers (denoted as Co3O4-NCNF) by a facile method. The Co3O4-NCNF possesses a high specific surface area(403.5 m2/g) and porous structure. The Co3O4-NCNF exhibits an excellent catalytic activity and long-time durability for both oxygen reduction and evolution reactions in alkaline solutions.

  16. Caractérisation des endommagements d'un composite Carbone/PA12 par émission acoustique

    OpenAIRE

    Philip, F.; Godin, N.; Deschanel, S.; M. Leroy, J.; Grosjean, F.; Courbon, J.

    2011-01-01

    International audience Cet article porte sur la caractérisation de l'endommagement par émission acoustique d'un matériau composite carbone / polyamide 12 (PA12) à fibres longues. L'objectif de ce travail est de discriminer en temps réel les différents types d'endommagement au sein du composite afin de mieux comprendre les mécanismes mis en jeu qui conduisent à la ruine de la structure. Une technique de classification supervisée a été utilisée. L'intérêt de cette technique est de pouvoir ét...

  17. Direct carbonization of cobalt-doped NH2-MIL-53(Fe) for electrocatalysis of oxygen evolution reaction

    Science.gov (United States)

    Han, Yujie; Zhai, Junfeng; Zhang, Lingling; Dong, Shaojun

    2015-12-01

    In this work, we synthesized high-performance electrocatalysts for oxygen evolution reaction (OER) by one-step carbonization of cobalt(Co)-doped NH2-MIL-53(Fe) with different molar ratios between Fe and Co. The results showed that the as-prepared composite with a molar ratio between Fe and Co = 1 : 3 and the calcination temperature of 550 °C displayed the best OER activity, denoted as MOF(Fe1-Co3)550N. The MOF(Fe1-Co3)550N possesses a microporous structure with a high Brunauer-Emmett-Teller (BET) surface area of 235.37 m2.g-1. It shows excellent OER catalytic behavior in 0.1 M KOH solution. The overpotential at 10 mA cm-2 is 0.39 V and the Tafel slope is 72.9 mV dec-1, which is comparable to that of the as-synthesized RuO2. The satisfactory results are attributed to the presence of pyridine N, Co3O4, the enlarged surface area and the micropore structures after calcination.In this work, we synthesized high-performance electrocatalysts for oxygen evolution reaction (OER) by one-step carbonization of cobalt(Co)-doped NH2-MIL-53(Fe) with different molar ratios between Fe and Co. The results showed that the as-prepared composite with a molar ratio between Fe and Co = 1 : 3 and the calcination temperature of 550 °C displayed the best OER activity, denoted as MOF(Fe1-Co3)550N. The MOF(Fe1-Co3)550N possesses a microporous structure with a high Brunauer-Emmett-Teller (BET) surface area of 235.37 m2.g-1. It shows excellent OER catalytic behavior in 0.1 M KOH solution. The overpotential at 10 mA cm-2 is 0.39 V and the Tafel slope is 72.9 mV dec-1, which is comparable to that of the as-synthesized RuO2. The satisfactory results are attributed to the presence of pyridine N, Co3O4, the enlarged surface area and the micropore structures after calcination. Electronic supplementary information (ESI) available: Additional information about the TEM images of different catalysts, XRD comparison of NH2-MIL-53(Fe) and other cobalt doped NH2-MIL-53(Fe), BET measurements of MOF(Fe1-Co3

  18. Chemical reactions at the graphitic step-edge: changes in product distribution of catalytic reactions as a tool to explore the environment within carbon nanoreactors

    Science.gov (United States)

    Lebedeva, Maria A.; Chamberlain, Thomas W.; Thomas, Alice; Thomas, Bradley E.; Stoppiello, Craig T.; Volkova, Evgeniya; Suyetin, Mikhail; Khlobystov, Andrei N.

    2016-06-01

    A series of explorative cross-coupling reactions have been developed to investigate the local nanoscale environment around catalytically active Pd(ii)complexes encapsulated within hollow graphitised nanofibers (GNF). Two new fullerene-containing and fullerene-free Pd(ii)Salen catalysts have been synthesised, and their activity and selectivity towards different substrates has been explored in nanoreactors. The catalysts not only show a significant increase in activity and stability upon heterogenisation at the graphitic step-edges inside the GNF channel, but also exhibit a change in selectivity affected by the confinement which alters the distribution of isomeric products of the reaction. Furthermore, the observed selectivity changes reveal unprecedented details regarding the location and orientation of the catalyst molecules inside the GNF nanoreactor, inaccessible by any spectroscopic or microscopic techniques, thus shedding light on the precise reaction environment inside the molecular catalyst-GNF nanoreactor.A series of explorative cross-coupling reactions have been developed to investigate the local nanoscale environment around catalytically active Pd(ii)complexes encapsulated within hollow graphitised nanofibers (GNF). Two new fullerene-containing and fullerene-free Pd(ii)Salen catalysts have been synthesised, and their activity and selectivity towards different substrates has been explored in nanoreactors. The catalysts not only show a significant increase in activity and stability upon heterogenisation at the graphitic step-edges inside the GNF channel, but also exhibit a change in selectivity affected by the confinement which alters the distribution of isomeric products of the reaction. Furthermore, the observed selectivity changes reveal unprecedented details regarding the location and orientation of the catalyst molecules inside the GNF nanoreactor, inaccessible by any spectroscopic or microscopic techniques, thus shedding light on the precise reaction

  19. Mechanisms of trichloramine removal with activated carbon: stoichiometric analysis with isotopically labeled trichloramine and theoretical analysis with a diffusion-reaction model.

    Science.gov (United States)

    Sakuma, Miki; Matsushita, Taku; Matsui, Yoshihiko; Aki, Tomoko; Isaka, Masahito; Shirasaki, Nobutaka

    2015-01-01

    This study investigated the mechanism by which activated carbon removes trichloramine, a byproduct of water treatment that has a strongly offensive chlorinous odor. A stoichiometrical mass balance for ¹⁵N before and after activated carbon treatment of laboratory-prepared ¹⁵N-labeled trichloramine solutions clearly revealed that the mechanism of trichloramine removal with activated carbon was not adsorption but rather reductive decomposition to nitrogen gas. There was a weak positive correlation between the surface decomposition rate constant of trichloramine and the concentration of basic functional groups on the surface of the carbon particles, the suggestion being that the trichloramine may have been reduced by sulfhydryl groups (-SH) on the activated carbon surface. Efficient decomposition of trichloramine was achieved with super powdered activated carbon (SPAC), which was prepared by pulverization of commercially available PAC into very fine particles less than 1 μm in diameter. SPAC could decompose trichloramine selectively, even when trichloramine and free chlorine were present simultaneously in water, the indication being that the strong disinfection capability of residual free chlorine could be retained even after trichloramine was effectively decomposed. The residual ratio of trichloramine after carbon contact increased somewhat at low water temperatures of 1-5 °C. At these low temperatures, biological treatment, the traditional method for control of a major trichloramine precursor (ammonium nitrogen), is inefficient. Even at these low temperatures, SPAC could reduce the trichloramine concentration to an acceptable level. A theoretical analysis with a diffusion-reaction model developed in the present study revealed that the increase in the trichloramine residual with decreasing water temperature was attributable to the temperature dependence of the rate of the reductive reaction rather than to the temperature dependence of the diffusive mass

  20. Low-temperature intermediates to oxygen reduction reaction catalysts based on amine-modified metal-loaded carbons. An XPS and ss-NMR investigation

    Energy Technology Data Exchange (ETDEWEB)

    Marzorati, Stefania [Università degli Studi di Milano, Dipartimento di Chimica, Via Golgi, 19, 20133 Milano (Italy); Ragg, Enzio M. [Università degli Studi di Milano, Dipartimento di Scienze per l’Alimentazione, la Nutrizione e l’Ambiente, Via Celoria, 2, 20133 Milano (Italy); Longhi, Mariangela, E-mail: mariangela.longhi@unimi.it [Università degli Studi di Milano, Dipartimento di Chimica, Via Golgi, 19, 20133 Milano (Italy); Formaro, Leonardo [Università degli Studi di Milano, Dipartimento di Chimica, Via Golgi, 19, 20133 Milano (Italy)

    2015-07-15

    Carbon functionalization is a major subject of interest in a number of project applications. Herein we report results on the characterization of nitrogen- and metal-loaded (Me = Fe, Co) carbon derivatives from low-T reaction steps before they are converted to catalysts for electrochemical oxygen reduction by later high-T treatments. The aim is to shed light on the state of carbon and carbon-bonded moieties before thermal modifications take place during any chosen high-T treatment. Though necessary for end catalyst activation, such thermal treatments make difficult to establish a relation between the starting reactants and finally obtained catalysts. Of interest to the paper are {sup 13}C, {sup 15}N solid-state NMR (ss-NMR) and high-resolution X-ray Photoelectron Spectroscopy (XPS) results on a commercial carbon that was reacted first with aliphatic di- and tri-amines and then with Fe, Co ions in room-T water. Data from natural abundance ss-{sup 15}N NMR in combination with XPS analysis were found especially relevant to assess that, in the adopted conditions, amines preferentially bind to carbon by creating alkylimino functional groups, which spontaneously form hydrous surface metal complexes with soluble Fe and Co ions. A chemical model is thus proposed for metal coordination in such C–N species. - Highlights: • A commercial carbon is nitrogen-doped by a low-T reaction with di- and tri-amines. • In the used conditions alkylimino groups are formed, able to act as ligands with metals (mainly Co). • A combination of {sup 13}C, {sup 15}N NMR and XPS is adopted for product characterization. • A model is proposed for the metal coordination with surface bonded groups.