Equalization equations in reactant resolution

Indian Academy of Sciences (India)

Unknown

given partitioning of the system in physical or functional space. The most frequently ... Then, the inter-reactant equilibrium is considered. The ... Global equilibrium. Even though the chemical potential in the case of global equilibrium is equalized by definition (see (1)), we repeat here the proof, for the current needs, using.

Synthesis, Characterization and Ion Exchange Properties of a New Composite of Inorganic Ion Exchanger： Polyacrylonitrile Cerium（IV） Molybdophosphate%Synthesis, Characterization and Ion Exchange Properties of a New Composite of Inorganic Ion Exchanger： Polyacrylonitrile Cerium（IV） Molybdophosphate

Institute of Scientific and Technical Information of China (English)

Ahmadi, Seyed Javad; Yavari, Ramin; Ashtari, Parviz＇; Gholipour, Vanik; Kamel, Leila; Rakhshandehru, Farokh

2012-01-01

In this work, the synthesis of the composite of cerium（IV） molybdophosphate （CMP） and polyacrylonitrile （PAN） was reported （CMP-PAN）. The material has been characterized by elemental and spectral （FT-IR）, X-ray and thermal （TGA） analysis. Also the size analysis of the composite was done by scanning electron microscopy （SEM）. Its chemical stability in acidic, basic and saline solutions and radiation stability up to 100 kGy total expose dose were assessed. Whereas the synthesized composite has ion exchange properties, its ion exchange capacity and behavior toward several metal ions were also investigated. Further, the distribution coefficients of the metal ions were calculated. Finally, the ability of the synthesized CMP-PAN composite for the decontamination of low level liquid waste （LLLW） was investigated.

Atmospheric Pressure Chemical Ionization Sources Used in The Detection of Explosives by Ion Mobility Spectrometry

Energy Technology Data Exchange (ETDEWEB)

Waltman, Melanie J. [New Mexico Inst. of Mining and Technology, Socorro, NM (United States)

2010-05-01

Explosives detection is a necessary and wide spread field of research. From large shipping containers to airline luggage, numerous items are tested for explosives every day. In the area of trace explosives detection, ion mobility spectrometry (IMS) is the technique employed most often because it is a quick, simple, and accurate way to test many items in a short amount of time. Detection by IMS is based on the difference in drift times of product ions through the drift region of an IMS instrument. The product ions are created when the explosive compounds, introduced to the instrument, are chemically ionized through interactions with the reactant ions. The identity of the reactant ions determines the outcomes of the ionization process. This research investigated the reactant ions created by various ionization sources and looked into ways to manipulate the chemistry occurring in the sources.

A dendrite-suppressing composite ion conductor from aramid nanofibres.

Science.gov (United States)

Tung, Siu-On; Ho, Szushen; Yang, Ming; Zhang, Ruilin; Kotov, Nicholas A

2015-01-27

Dendrite growth threatens the safety of batteries by piercing the ion-transporting separators between the cathode and anode. Finding a dendrite-suppressing material that combines high modulus and high ionic conductance has long been considered a major technological and materials science challenge. Here we demonstrate that these properties can be attained in a composite made from Kevlar-derived aramid nanofibres assembled in a layer-by-layer manner with poly(ethylene oxide). Importantly, the porosity of the membranes is smaller than the growth area of the dendrites so that aramid nanofibres eliminate 'weak links' where the dendrites pierce the membranes. The aramid nanofibre network suppresses poly(ethylene oxide) crystallization detrimental for ion transport, giving a composite that exhibits high modulus, ionic conductivity, flexibility, ion flux rates and thermal stability. Successful suppression of hard copper dendrites by the composite ion conductor at extreme discharge conditions is demonstrated, thereby providing a new approach for the materials engineering of solid ion conductors.

The study on the ion exchange behavior of metal ions using composite ion exchange resin

Energy Technology Data Exchange (ETDEWEB)

Kim, Kukki; Lee, Kunjai [Nuclear Engineering Department Korea Advanced Institute of Science and Technology, Taejon (Korea, Republic of); Kim, Youngkyun [Korea Institute of Nuclear Safety, Daejon (Korea, Republic of); Lee, Sangjin; Yang, Hoyeon; Ha, Jonghyun [Korea Hydro and Nuclear Power Co., Daejeon (Korea, Republic of)

2002-04-15

In this study, a series of stepwise procedures to prepare a new organic-inorganic composite magnetic resin with phenol sulphonic-formaldehyde and freshly formed iron ferrite was established, based upon wet-and-neutralization method for synthesizing iron ferrite and pearl-polymerization method for synthesizing rigid bead-type composite resin. And a separation of metal ions in the liquid radioactive waste have been performed using organic-inorganic composite magnetic resin with phenol sulphonic-formaldehyde and freshly formed iron ferrite. The PSF-F (phenol sulphonic formaldehyde-iron ferrite) composite resin prepared by the above method shows stably high removal efficiency to Co(II), Fe, Cs species from wastewater in a wide range of solution pH. The wide range of applicable solution pH (i. e. pH 4.0 to 10.3) implies that the PSF-F composite resin overcomes the limitations of the conventional ferrite process which is practically applicable only to alkaline conditions. The experiment proceeded using batch reactor in a constant temperature with water bath. The experiments divided into three parts. The first one is TG/DTA (Thermogravimetry / Differential Thermal Analysis) which can analyze the trend of pyrolysis of PSF-F ion exchanger. The Second one is equilibrium experiment in which the separation factor of metal ions and Langmuir, Freundlich isotherm was achieved. The last one is kinetics experiment in which the equilibrium reaction time and removal efficiency is estimated.

The study on the ion exchange behavior of metal ions using composite ion exchange resin

International Nuclear Information System (INIS)

Kim, Kukki; Lee, Kunjai; Kim, Youngkyun; Lee, Sangjin; Yang, Hoyeon; Ha, Jonghyun

2002-01-01

In this study, a series of stepwise procedures to prepare a new organic-inorganic composite magnetic resin with phenol sulphonic-formaldehyde and freshly formed iron ferrite was established, based upon wet-and-neutralization method for synthesizing iron ferrite and pearl-polymerization method for synthesizing rigid bead-type composite resin. And a separation of metal ions in the liquid radioactive waste have been performed using organic-inorganic composite magnetic resin with phenol sulphonic-formaldehyde and freshly formed iron ferrite. The PSF-F (phenol sulphonic formaldehyde-iron ferrite) composite resin prepared by the above method shows stably high removal efficiency to Co(II), Fe, Cs species from wastewater in a wide range of solution pH. The wide range of applicable solution pH (i. e. pH 4.0 to 10.3) implies that the PSF-F composite resin overcomes the limitations of the conventional ferrite process which is practically applicable only to alkaline conditions. The experiment proceeded using batch reactor in a constant temperature with water bath. The experiments divided into three parts. The first one is TG/DTA (Thermogravimetry / Differential Thermal Analysis) which can analyze the trend of pyrolysis of PSF-F ion exchanger. The Second one is equilibrium experiment in which the separation factor of metal ions and Langmuir, Freundlich isotherm was achieved. The last one is kinetics experiment in which the equilibrium reaction time and removal efficiency is estimated

Process for producing uranium oxide rich compositions from uranium hexafluoride

International Nuclear Information System (INIS)

DeHollander, W.R.; Fenimore, C.P.

1978-01-01

Conversion of gaseous uranium hexafluoride to a uranium dioxide rich composition in the presence of an active flame in a reactor defining a reaction zone is achieved by separately introducing a first gaseous reactant comprising a mixture of uranium hexafluoride and a reducing carrier gas, and a second gaseous reactant comprising an oxygen-containing gas. The reactants are separated by a shielding gas as they are introduced to the reaction zone. The shielding gas temporarily separates the gaseous reactants and temporarily prevents substantial mixing and reacting of the gaseous reactants. The flame occurring in the reaction zone is maintained away from contact with the inlet introducing the mixture to the reaction zone. After suitable treatment, the uranium dioxide rich composition is capable of being fabricated into bodies of desired configuration for loading into nuclear fuel rods. Alternatively, an oxygen-containing gas as a third gaseous reactant is introduced when the uranium hexafluoride conversion to the uranium dioxide rich composition is substantially complete. This results in oxidizing the uranium dioxide rich composition to a higher oxide of uranium with conversion of any residual reducing gas to its oxidized form

Generation of H-, D- ions on composite surfaces with application to surface/plasma ion source systems

International Nuclear Information System (INIS)

Hiskes, J.R.; Karo, A.M.; Wimmer, E.; Freeman, A.J.; Chubb, S.R.

1983-01-01

We review some salient features of the experimental and theoretical data pertaining to hydrogen negative ion generation on minimum-work-function composite surfaces consisting of Cs/transition metal substrates. Cesium or hydrogen ion bombardment of a cesium-activated negatively-biased electrode exposed to a cesium-hydrogen discharge results in the release of hydrogen negative ions. These ions originate through desorbtion of hydrogen particles by incident cesium ions, desorbtion by incident hydrogen ions, and by backscattering of incident hydrogen. Each process is characterized by a specific energy and angular distribution. The calculation of ion formation in the crystal selvage region is discussed for different approximations to the surface potential. An ab initio, all-electron, local density functional model for the composite surface electronics is discussed

Experimental investigation of laminar LPG-H{sub 2} jet diffusion flame with preheated reactants

Energy Technology Data Exchange (ETDEWEB)

D.P. Mishra; P. Kumar [Indian Institute of Technology, Kanpur (India). Combustion Laboratory, Department of Aerospace Engineering

2008-10-15

This paper presents an experimental investigation of the effect of H{sub 2} addition on flame length, soot free length fraction (SFLF), flame radiant fraction, gas temperature and emission level in LPG-H{sub 2} composite fuel jet diffusion flame for two preheated cases namely, (i) preheated air and (ii) preheated air and fuel. Results show that the H{sub 2} addition leads to a reduction in flame length which may be caused due to an increased gas temperature. Besides this, the flame length is also observed to be reduced with increasing reactants temperature. The soot free length fraction (SFLF) increases as H{sub 2} is added to fuel stream. This might have been caused by decrease in the C/H ratio in the flame and is favorable to attenuate PAH formation rate. Interestingly, the SFLF is observed to be reduced with increasing reactants temperature that may be due to reduction in induction period of soot formation caused by enhanced flame temperature. Moreover, the decreased radiant heat fraction with hydrogen addition is pertinent with the reduction in soot concentration level. The reduction in NOx emission level with H{sub 2} addition to the fuel stream is also observed. On the contrary, NOx emission level is found to be enhanced significantly with reactant temperature that can be attributed to the increase in thermal NOx through Zeldovich mechanism. 31 refs., 4 figs., 2 tabs.

Analysis of Ion Composition Estimation Accuracy for Incoherent Scatter Radars

Science.gov (United States)

Martínez Ledesma, M.; Diaz, M. A.

2017-12-01

The Incoherent Scatter Radar (ISR) is one of the most powerful sounding methods developed to estimate the Ionosphere. This radar system determines the plasma parameters by sending powerful electromagnetic pulses to the Ionosphere and analyzing the received backscatter. This analysis provides information about parameters such as electron and ion temperatures, electron densities, ion composition, and ion drift velocities. Nevertheless in some cases the ISR analysis has ambiguities in the determination of the plasma characteristics. It is of particular relevance the ion composition and temperature ambiguity obtained between the F1 and the lower F2 layers. In this case very similar signals are obtained with different mixtures of molecular ions (NO2+ and O2+) and atomic oxygen ions (O+), and consequently it is not possible to completely discriminate between them. The most common solution to solve this problem is the use of empirical or theoretical models of the ionosphere in the fitting of ambiguous data. More recent works take use of parameters estimated from the Plasma Line band of the radar to reduce the number of parameters to determine. In this work we propose to determine the error estimation of the ion composition ambiguity when using Plasma Line electron density measurements. The sensibility of the ion composition estimation has been also calculated depending on the accuracy of the ionospheric model, showing that the correct estimation is highly dependent on the capacity of the model to approximate the real values. Monte Carlo simulations of data fitting at different signal to noise (SNR) ratios have been done to obtain valid and invalid estimation probability curves. This analysis provides a method to determine the probability of erroneous estimation for different signal fluctuations. Also it can be used as an empirical method to compare the efficiency of the different algorithms and methods on when solving the ion composition ambiguity.

CRRES observations of stormtime ring current ion composition

International Nuclear Information System (INIS)

Roeder, J.L.; Fennell, J.F.; Chen, M.W.; Grande, M.; Livi, S.; Schulz, M.

1996-01-01

The Magnetospheric Ion Composition Spectrometer onboard the CRRES spacecraft provided mass and charge state composition data for positive ions in the energy-per-charge range 1 endash 426 keV/e. The CRRES data is compared to the AMPTE/CCE observations during a moderately large geomagnetic storm on 4 June 1991. The results are compared to observations of large storms by CRRES and by the AMPTE/CCE spacecraft. The CRRES data show that oxygen ions formed 29% of the total measured ion energy density at L=3 endash 5 during the storm recovery phase. This result implies that domination of the plasma by oxygen ions may not be necessary to produce the observed rapid initial recovery of the Dst magnetic index. A preliminary test of the Dessler-Parker-Sckopke relation between the ion energy and the global magnetic perturbation shows that the observed particle fluxes during the 4 June 1991 storm could account for only 40 endash 70% of the variation of Dst. copyright 1996 American Institute of Physics

Laboratory studies of ion-molecule reactions and interstellar chemistry

International Nuclear Information System (INIS)

Koyano, Inosuke

1989-01-01

Several types of laboratory studies have been performed on ion-molecule reactions relevant to the formation of the interstellar molecules. Special emphasis is placed on the formation, structure, and reactivity of the C 3 H 3 + ions, which are believed to play a key role in interstellar chemistry. When these ions are produced by the reaction of C 3 H 4+ with C 3 H 4 in a beam-gas arrangement, their times-of-flight (TOF) show abnormally broad distributions regardless of the sources of the reactant C 3 H 4 + ion (photoionization of allene, propyne, the cyclopropene) and the nature of the neutral reactant, while all other product ions from the same reaction show sharp TOF distributions. On the other hand, all C 3 H 3 + ions produced by unimolecular decomposition of energetic C 3 H 4 + ions show sharp TOF distribution. The peculiarity of the C 3 H 3 + ions manifested in these and other experiments is discussed in conjunction with interstellar chemistry

Liquid Water Transport in the Reactant Channels of Proton Exchange Membrane Fuel Cells

Science.gov (United States)

Banerjee, Rupak

Water management has been identified as a critical issue in the development of PEM fuel cells for automotive applications. Water is present inside the PEM fuel cell in three phases, i.e. liquid phase, vapor phase and mist phase. Liquid water in the reactant channels causes flooding of the cell and blocks the transport of reactants to the reaction sites at the catalyst layer. Understanding the behavior of liquid water in the reactant channels would allow us to devise improved strategies for removing liquid water from the reactant channels. In situ fuel cell tests have been performed to identify and diagnose operating conditions which result in the flooding of the fuel cell. A relationship has been identified between the liquid water present in the reactant channels and the cell performance. A novel diagnostic technique has been established which utilizes the pressure drop multiplier in the reactant channels to predict the flooding of the cell or the drying-out of the membrane. An ex-situ study has been undertaken to quantify the liquid water present in the reactant channels. A new parameter, the Area Coverage Ratio (ACR), has been defined to identify the interfacial area of the reactant channel which is blocked for reactant transport by the presence of liquid water. A parametric study has been conducted to study the effect of changing temperature and the inlet relative humidity on the ACR. The ACR decreases with increase in current density as the gas flow rates increase, removing water more efficiently. With increase in temperature, the ACR decreases rapidly, such that by 60°C, there is no significant ACR to be reported. Inlet relative humidity of the gases does change the saturation of the gases in the channel, but did not show any significant effect on the ACR. Automotive powertrains, which is the target for this work, are continuously faced with transient changes. Water management under transient operating conditions is significantly more challenging and has not

Chiral Selectivity in Inter-reactant Recognition and Electron Transfer of the Oxidation of Horse Heart Cytochrome c by Trioxalatocobaltate(III)

DEFF Research Database (Denmark)

Nazmutdinov, Renat R.; Bronshtein, Michael D.; Zinkicheva, Tamara T.

2016-01-01

We have studied electron transfer between cytochrome c and the chiral transition-metal complex pair Λ- and Δ-[Co(Ox)3]3− (Ox2− = oxalate) via strong ion-pair formation. Chirality was found in both ion-pair formation and electron transfer, with the Λ enantiomer the more strongly bound and faster r...... reacting. Investigations of the chirality using electron-transfer theory combined with quantum-chemical and statistical-mechanical calculations showed that chirality is solely in inter-reactant interaction and electronic overlap.......We have studied electron transfer between cytochrome c and the chiral transition-metal complex pair Λ- and Δ-[Co(Ox)3]3− (Ox2− = oxalate) via strong ion-pair formation. Chirality was found in both ion-pair formation and electron transfer, with the Λ enantiomer the more strongly bound and faster...

Removal of Cu 2+ Ions from Aqueous Medium Using Clinoptilolite/Emeraldine Base Composite

Directory of Open Access Journals (Sweden)

Silviya I. Lavrova

2016-12-01

Full Text Available The aim of this study was to investigate the removal efficiency of in situ synthesized composites consisted of emeraldine base and clinoptilolite on copper ions removal from aqueous medium. Two composite materials (Composite I and Composite II with different quantity of clinoptilolite were synthesised. The influence of the composite dosage, the contact time and the initial copper ions concentration has been studied. The results show that the significant removal of the copper ions becomes at the first minute of the contact between the composite material and the aqueous medium and the longer contact time leads to increasing of the copper ions removal. The removal efficiency at the 1st minute was 57.5% and 77.3% using Composite Iand Composite II, respectively. Maximum removal efficiency of 87.3% and 96.8% was achieved at the same dosage of Composite I and Composite II, respectively, at contact time of 360 minutes and temperature of 24 °C.

Thermal ion-molecule reactions in oxygen-containing molecules

International Nuclear Information System (INIS)

Kumakura, Minoru

1981-02-01

The energetics of ions and the thermal ion-molecule reactions in oxygen-containing molecules have been studied with a modified time-of-flight mass spectrometer. It was found that the translational energy of ion can be easily obtained from analysis of the decay curve using the time-of-flight mass spectrometer. The condensation-elimination reactions proceeded via cross- and homo-elimination mechanism in which the nature of intermediate-complex could be correlated with the nature of reactant ion. It was elucidated that behavior of poly-atomic oxygen-containing ions on the condensation-elimination reactions is considerably influenced by their oxonium ion structures having functional groups. In addition, the rate constants of the condensation-elimination reactions have affected with the energy state of reactant ion and the dipole moment and/or the polarizability of neutral molecule. It was clarified that the rate constants of the ion-molecule clustering reactions in poly-atomic oxygen-containing molecules such as cyclic ether of six member rings are very large and the cluster ions are stable owing to the large number of vibrational degree of freedom in the cluster ions. (author)

Complex nonlinear behaviour of a fixed bed reactor with reactant recycle

DEFF Research Database (Denmark)

Recke, Bodil; Jørgensen, Sten Bay

1999-01-01

The fixed bed reactor with reactant recycle investigated in this paper can exhibit periodic solutions. These solutions bifurcate from the steady state in a Hopf bifurcation. The Hopf bifurcation encountered at the lowest value of the inlet concentration turns the steady state unstable and marks......,that the dynamic behaviour of a fixed bed reactor with reactant recycle is much more complex than previously reported....

Investigation of the composition of an ion beam produced using a multi arc ion source

Energy Technology Data Exchange (ETDEWEB)

Engelko, V [Efremov Institute of Electrophysical Apparatus, St. Petersburg (Russian Federation); Giese, H; Schalk, S [Forschungszentrum Karlsruhe (Germany). INR; Mishin, M; Tsibin, O Y [St. Petersburg State Technical Univ. (Russian Federation)

1997-12-31

Complementing the diode and beam transport optimization studies currently performed at FZK Karlsruhe on the proton-beam-facility PROFA, supplementary investigations were run at the St. Petersburg State University, focusing on ion beam divergence and composition measurements using the TOF techniques. To ensure direct transferability of the results to the PROFA facility, these measurements were made on a scaled-down replica of the PROFA diode, comprising an array of small polyethylene flash-over plasma sources and a grid extraction system. Only the results of the beam composition measurements are presented, and the following conclusions are made: (i) The ion beam contains H and C ions and heavier constituents that remain to be identified. (ii) The beam composition changes significantly with the total number of shots: While H{sup +} ions predominated in the starting phase of the experiments, heavier components outweighed them later on, presumably due to hydrogen depletion of the surface layer of the anode polyethylene units. (iii) Reconditioning of the polyethylene units may be possible by running the diode at higher currents (self-cleaning) or by cutting off a surface layer. (author). 7 figs., 3 refs.

Scintillation screen applications in a vacuum arc ion source with composite hydride cathode

Science.gov (United States)

Wang, X. H.; Tuo, X. G.; Yang, Z.; Peng, Y. F.; Li, J.; Lv, H. Y.; Li, J. H.; Long, J. D.

2018-05-01

Vacuum arc ion source with composite hydride cathode was developed to produce intense ion beams which can be applied in particle accelerator injections. Beam profile and beam composition are two fundamental parameters of the beam for the vacuum arc ion source in such specific applications. An aluminum-coated scintillation screen with an ICCD camera readout was used to show the space-time distribution of the beam directly. A simple magnetic analysis assembly with the scintillation screen shows the beam composition information of this kind ion source. Some physical and technical issues are discussed and analyzed in the text.

Metal hydride compositions and lithium ion batteries

Energy Technology Data Exchange (ETDEWEB)

Young, Kwo; Nei, Jean

2018-04-24

Heterogeneous metal hydride (MH) compositions comprising a main region comprising a first metal hydride and a secondary region comprising one or more additional components selected from the group consisting of second metal hydrides, metals, metal alloys and further metal compounds are suitable as anode materials for lithium ion cells. The first metal hydride is for example MgH.sub.2. Methods for preparing the composition include coating, mechanical grinding, sintering, heat treatment and quenching techniques.

Application of Some Synthesized Polymeric Composite Resins for Removal of Some Metal Ions

International Nuclear Information System (INIS)

El-Zahhhar, A.A.; Abdel-Aziz, H.M.; Siyam, T.

2005-01-01

The ion-exchange and sorption characteristic of new polymeric composite resins, prepared by gamma radiation were experimentally studied. The composite resins shows high uptake for Co(II) and Eu(III) ions in aqueous solutions in wide range of ph. The selectivity of the resins to Co (II) or Eu (III) species in the presence of some competing ions and complexing agents (as Na + , Fe 3+ , EDTA Na 2 , etc.) was compared. Various factors that could affect the sorption behaviors of metal ions (Co (II) and Eu (III)) on the prepared polymeric composite resins were studied such as ionic strength, Contact time, volume mass ratio

New Composite Sorbents for Caesium and Strontium Ions Sorption

Directory of Open Access Journals (Sweden)

Mykola Kartel

2017-06-01

Full Text Available Composite lignocellulose-inorganic sorbents derived from plant residues of agriculture and food industry, modified with ferrocyanides of d-metals and hydrated antimony pentoxide were prepared. Caesium and strontium ions removal from water was tested by radiotracer method. Sorption of heavy metal ions, methylene blue, gelatin, vitamin B12 was also studied.

Ion Composition of Comet 19P/Borrelly as Measured by the PEPE Ion Mass Spectrometer on DS1

Science.gov (United States)

Nordholt, J. E.; Reisenfeld, D. B.; Wiens, R. C.; Gary, P.

2002-12-01

Cometary compositions are of great interest because they hold important clues to the formation of the outer solar system, and to the sources of volatiles in the solar system, including the terrestrial planets. In order to understand the primordial compositions of cometary nuclei, it is important to also understand their evolution, as many of the comets most accessible to spacecraft are highly evolved. It is also important to understand the ion and neutral chemistry that occurs in the coma surrounding the nucleus if the coma ion composition is to be used to determine the original composition of the nucleus. Deep Space One (DS1) was only the second spacecraft, after Giotto, to use an ion mass-resolving instrument to explore cometary coma compositions in-situ, which it did during the flyby of Comet Borrelly on September 22, 2001. Borrelly is significantly more evolved than Halley. In addition, the encounter occurred at a significantly greater distance from the sun (1.36 AU vs 0.9 AU for Giotto at Halley). The Plasma Experiment for Planetary Exploration (PEPE) on board DS1 was capable of resolving electron and ion energy, angle of incidence, and ion mass composition. The PEPE ion data from the seven minutes surrounding closest approach (2171 km) have been extensively analyzed. The instrument response was modeled using SIMION and TRIM codes for all of the major species through 20 AMU plus CO (at its operating voltage PEPE was very insensitive to heavier molecules). Chi-squared minimization analysis is being carried out to determine the best fit and the uncertainties. Preliminary results for the predominant heavy ions are OH+ at (72 +/- 9)% of the total water-group ion density, H2O+ at (25 +/- 7)%, CH3+ at (5 +/- 3)%, and O+ at (4 +/- 5)%. Uncertainties are quoted at the 90% confidence level. Comparison with reported Halley compositions from Giotto shows that Borrelly clearly has a lower H3O+ abundance (< 9%), consistent with a more evolved comet. The presence of

Gas-phase reaction rate constants for atmospheric pressure ionization in ion-mobility spectrometry

International Nuclear Information System (INIS)

Vandiver, V.J.

1987-01-01

Ion-mobility spectrometry (IMS) is an instrumental technique in which gaseous ions are formed from neutral molecules by proton and charge transfer from reactant ions through collisional ionization. An abbreviated rate theory has been proposed for atmospheric pressure ionization (API) in IMS, but supporting experimental measurements have not been reported. The objectives of this thesis were (1) assessment of existing API rate theory using positive and negative product ions in IMS, (2) measurement of API equilibria and kinetics for binary mixtures, and (3) investigating of cross-ionizations with multiple-product ions in API reactions. Although IMS measurements and predictions from rate theory were comparable, shapes and slopes of response curves for both proton transfer and electron capture were not described exactly by existing theory. In particular, terms that are needed for calculation of absolute rate constants were unsuitable in the existing theory. These included recombination coefficients,initial number of reactant ions, and opposing ion densities

Composition of heavy ions in solar energetic particle events

International Nuclear Information System (INIS)

Fan, C.Y.; Gloeckler, G.

1983-01-01

The elemental, charge state, and isotopic composition of approximately 1 to 20 MeV per nucleon ions in solar energetic particle (SEP) events was determined and current understanding of the nature of solar and interplanetary processes which may explain the observations are outlined. The composition within individual SEP events may vary both with time and energy, and will in general be different from that in other SEP events. Average values of relative abundances measured in a large number of SEP events, however are found to be roughly energy independent in the approximately 1 to approximately 20 MeV per nucleon range, and show a systematic deviation from photospheric abundances which seem to be organized in terms of the first ionization potential of the ion. Direct measurements of the charge states of SEPs have revealed the surprisingly common presence of energetic He(+) along with heavy ions with typical coronal ionization states. High resolution measurements of isotopic abundance ratios in a small number of SEP events show these to be consistent with the universal composition except for the puzzling overabundance of the SEP Ne-22 relative to this isotopes ratio in the solar wind

Low temperature synthesis of Mo2C/W2C superlattices via ultra-thin modulated reactants

International Nuclear Information System (INIS)

Johnson, C.D.; Johnson, D.C.

1996-01-01

The authors report here a synthesis method of preparing carbide superlattices using ultra-thin modulated reactants. Initial investigations into the synthesis of the binary systems, Mo 2 C and W 2 C using ultra-thin modulated reactants revealed that both can be formed at relatively low temperatures (500 and 600 C respectively). DSC and XRD data suggested a two step reaction pathway involving interdiffusion of the initial modulated reactant followed by crystallization of the final product, if the modulation length is on the order of 10 angstrom. This information was used to form Mo 2 C/W 2 C superlattices using the structure of the ultra-thin modulated reactant to control the final superlattice period. Relatively large superlattice modulations were kinetically trapped by having several repeat units of each binary within the total repeat of the initial reactant. DSC and XRD data again are consistent with a two step reaction pathway leading to the formation of carbide superlattices

A SIFT study of the reactions of H2ONO+ ions with several types of organic molecules

Science.gov (United States)

Smith, David; Wang, Tianshu; Spanel, Patrik

2003-11-01

A selected ion flow tube (SIFT) study has been carried out of the reactions of hydrated nitrosonium ions, NO+H2O, which theory has equated to protonated nitrous acid ions, H2ONO+. One objective of this study was to investigate if this ion exhibits the properties of both a cluster ion and a protonated acid in their reactions with a variety of organic molecules. The chosen reactant molecules comprise two each of the following types--amines, terpenes, aromatic hydrocarbons, esters, carboxylic acids, ketones, aldehydes and alcohols. The reactant H2ONO+ (NO+H2O) ions are formed in a discharge ion source and injected into helium carrier gas where they are partially vibrationally excited and partially dissociated to NO+ ions. Hence, the reactions of the H2ONO+ ions had to be studies simultaneously with NO+ ions, the reactions of the latter ions readily being studied by selectively injecting NO+ ions into the carrier gas. The results of this study indicate that the H2ONO+ ions undergo a wide variety of reaction processes that depend on the properties of the reactant molecules such as their ionisation energies and proton affinities. These processes include charge transfer with compounds, M, that have low ionisation energies (producing M+), proton transfer with compounds possessing large proton affinities (MH+), hydride ion transfer (M---H+), alkyl radical (M---R+), alkoxide radical transfer (M---OR+), ion-molecule association (NO+H2OM) and ligand switching (NO+M), producing the ions given in parentheses.

Survey of 0.1- to 16-keV/e plasma sheet ion composition

International Nuclear Information System (INIS)

Lennartsson, W.; Shelley, E.G.

1986-01-01

A large statistical survey of the 0.1- to 16-keV/e plasma sheet ion composition has been carried out using data obtained by the Plasma Composition Experiment on ISEE 1 between 10 and 23 R/sub E/ during 1978 and 1979. This survey includes more than 10 times the quantity of data used in earlier studies of the same topic and makes it possible to investigate in finer detail the relationship between the ion composition and the substorm activity. The larger data base also makes it possible for the first time to study the spatial distribution of the principal ion species. As found in previous studies, the ion composition has a large variance at any given value of the AE index, but a number of distinct trends emerge when the data are averaged at each activity level. During quiet conditions the plasma sheet is dominated by ions of solar origin (H + and He ++ ), as found in earlier studies, and these ions are most numerous during extended periods of very low activity (AE< or approx. =30 γ). The quiet time density of these ions is particularly large in the flanks of the plasma sheet (GSM Yapprox. +- 10 R/sub E/), where it is about twice as large as it is near the central axis of the plasma sheet (Y = Z = 0). In contrast, the energy of these ions peaks near the central axis

Composition of heavy ions in solar energetic particle events

International Nuclear Information System (INIS)

Fan, C.Y.; Gloeckler, G.

1983-01-01

Recent advances in determining the elemental, charge state, and isotopic composition of approximatelt 1 to 20 MeV per nucleon ions in solar energetic particle (SEP) events and outline our current understanding of the nature of solar and interplanetary processes which may explain the observations. Average values of relative abundances measured in a large number of SEP events were found to be roughly energy independent in the approx. 1 to approx. 20 MeV per nucleon range, and showed a systematic deviation from photospheric abundances which seems to be organized in terms of the first ionization potential of the ion. Direct measurements of the charge states of SEPs revealed the surprisingly common presence of energetic He(+) along with heavy ion with typically coronal ionization states. High resolution measurements of isotopic abundance ratios in a small number of SEP events showed these to be consistent with the universal composition except for the puzzling overabundance of the SEP(22)Ne/(20)Ne relative to this isotopes ratio in the solar wind. The broad spectrum of observed elemental abundance variations, which in their extreme result in composition anomalies characteristic of (3)He rich, heavy ion rich and carbon poor SEP events, along with direct measurements of the ionization states of SEPs provided essential information on the physical characteristics of, and conditions in the source regions, as well as important constraints to possible models for SEP production

Ion beam modifications of near-surface compositions in ternary alloys

International Nuclear Information System (INIS)

Lam, N.Q.; Tang, S.; Yacout, A.M.; Rehn, L.E.; Stubbins, J.F.

1990-11-01

Changes in the surface and subsurface compositions of ternary alloys during elevated-temperature sputtering with inert-gas ions were investigated. Theoretically, a comprehensive kinetic model which includes all the basic processes, such as preferential sputtering, displacement mixing, Gibbsian segregation, radiation-enhanced diffusion and radiation-induced segregation, was developed. This phenomenological approach enabled to predict the effects of each individual process or of a combination of processes on the compositional modification in model alloys. Experimentally, measurements of compositional changes at the surface of a Ag-40at%Au -- 20at%Cu alloy during 3-keV Ne + bombardment at various temperatures were made, using ion scattering spectroscopy. These measurements were interpreted on the basis of the results of theoretical modeling. 8 refs., 2 figs

Ion beam studies. Part 5 - the computer simulation of composite ion implantation profiles

International Nuclear Information System (INIS)

Freeman, J.H.; Booker, D.V.

1977-01-01

The computer simulation of composite ion implantation profiles produced by continuous energy programming and by discrete multiple dose doping is described. It is shown that precise matching of the computed profile to various uniform and power-law distributions can be achieved. (author)

THE INFLUENCE OF BENZENE AS A TRACE REACTANT IN TITAN AEROSOL ANALOGS

Energy Technology Data Exchange (ETDEWEB)

Trainer, Melissa G. [Planetary Environments Laboratory, Code 699, NASA Goddard Space Flight Center, Greenbelt, MD 20771 (United States); Sebree, Joshua A. [NASA Postdoctoral Program Fellow, Code 699, Goddard Space Flight Center, Greenbelt, MD 20771 (United States); Heidi Yoon, Y.; Tolbert, Margaret A., E-mail: melissa.trainer@nasa.gov [Cooperative Institute for Research in Environmental Sciences, University of Colorado at Boulder, Box 216 UCB, Boulder, CO 80309 (United States)

2013-03-20

Benzene has been detected in Titan's atmosphere by Cassini instruments, with concentrations ranging from sub-ppb in the stratosphere to ppm in the ionosphere. Sustained levels of benzene in the haze formation region could signify that it is an important reactant in the formation of Titan's organic aerosol. To date, there have not been laboratory investigations to assess the influence of benzene on aerosol properties. We report a laboratory study on the chemical composition of organic aerosol formed from C{sub 6}H{sub 6}/CH{sub 4}/N{sub 2} via far ultraviolet irradiation (120-200 nm). The compositional results are compared to those from aerosol generated by a more ''traditional Titan'' mixture of CH{sub 4}/N{sub 2}. Our results show that even a trace amount of C{sub 6}H{sub 6} (10 ppm) has significant impact on the chemical composition and production rates of organic aerosol. There are several pathways by which photolyzed benzene may react to form larger molecules, both with and without the presence of CH{sub 4}, but many of these reaction mechanisms are only beginning to be explored for the conditions at Titan. Continued work investigating the influence of benzene in aerosol growth will advance understanding of this previously unstudied reaction system.

On the mechanism of effective chemical reactions with turbulent mixing of reactants and finite rate of molecular reactions

Energy Technology Data Exchange (ETDEWEB)

Vorotilin, V. P., E-mail: VPVorotilin@yandex.ru [Russian Academy of Sciences, Institute of Applied Mechanics (Russian Federation)

2017-01-15

A generalization of the theory of chemical transformation processes under turbulent mixing of reactants and arbitrary values of the rate of molecular reactions is presented that was previously developed for the variant of an instantaneous reaction [13]. The use of the features of instantaneous reactions when considering the general case, namely, the introduction of the concept of effective reaction for the reactant volumes and writing a closing conservation equation for these volumes, became possible due to the partition of the whole amount of reactants into “active” and “passive” classes; the reactants of the first class are not mixed and react by the mechanism of instantaneous reactions, while the reactants of the second class approach each other only through molecular diffusion, and therefore their contribution to the reaction process can be neglected. The physical mechanism of reaction for the limit regime of an ideal mixing reactor (IMR) is revealed and described. Although formally the reaction rate in this regime depends on the concentration of passive fractions of the reactants, according to the theory presented, the true (hidden) mechanism of the reaction is associated only with the reaction of the active fractions of the reactants with vanishingly small concentration in the volume of the reactor. It is shown that the rate constant of fast chemical reactions can be evaluated when the mixing intensity of reactants is much less than that needed to reach the mixing conditions in an IMR.

Origin of energetic ions in the polar cusp inferred from ion composition measurements by the Viking satellite

Directory of Open Access Journals (Sweden)

G. Kremser

1995-06-01

Full Text Available The magnetospheric ion composition spectrometer MICS on the Swedish Viking satellite provided measurements of the ion composition in the energy range 10.1 keV/e\\leqE/Q\\leq326.0 keV/e. Data obtained during orbit 842 were used to investigate the ion distribution in the northern polar cusp and its vicinity. The satellite traversed the outer ring current, boundary region, cusp proper and plasma mantle during its poleward movement. H+ and He++ ions were encountered in all of these regions. He+ ions were present only in the ring current. The number of O+ and O++ ions was very small. Heavy high-charge state ions typical for the solar wind were observed for the first time, most of them in the poleward part of the boundary region and in the cusp proper. The H+ ions exhibited two periods with high intensities. One of them, called the BR/CP event, appeared at energies up to 50 keV. It started at the equatorward limit of the boundary region and continued into the cusp proper. Energy spectra indicate a ring current origin for the BR/CP event. Pitch angle distributions show downward streaming of H+ ions at its equatorward limit and upward streaming on the poleward side. This event is interpreted as the result of pitch angle scattering of ring current ions by fluctuations in the magnetopause current layer in combination with poleward convection. The other of the two periods with high H+ ion intensities, called the accelerated ion event, was superimposed on the BR/CP event. It was restricted to energies \\leq15 keV and occurred in the poleward part of the boundary region. This event is regarded as the high-energy tail of magnetosheath ions that were accelerated while penetrating into the magnetosphere. The cusp region thus contains ions of magnetospheric as well as of magnetosheath origin. The appearance of the ions depends, in addition to the ion source, on the magnetic field configuration and dynamic processes inside and close to the cusp.

Geotail observations of plasma sheet ion composition over 16 years: On variations of average plasma ion mass and O+ triggering substorm model

Science.gov (United States)

Nosé, M.; Ieda, A.; Christon, S. P.

2009-07-01

We examined long-term variations of ion composition in the plasma sheet, using energetic (9.4-212.1 keV/e) ion flux data obtained by the suprathermal ion composition spectrometer (STICS) sensor of the energetic particle and ion composition (EPIC) instrument on board the Geotail spacecraft. EPIC/STICS observations are available from 17 October 1992 for more than 16 years, covering the declining phase of solar cycle 22, all of solar cycle 23, and the early phase of solar cycle 24. This unprecedented long-term data set revealed that (1) the He+/H+ and O+/H+ flux ratios in the plasma sheet were dependent on the F10.7 index; (2) the F10.7 index dependence is stronger for O+/H+ than He+/H+; (3) the O+/H+ flux ratio is also weakly correlated with the ΣKp index; and (4) the He2+/H+ flux ratio in the plasma sheet appeared to show no long-term trend. From these results, we derived empirical equations related to plasma sheet ion composition and the F10.7 index and estimated that the average plasma ion mass changes from ˜1.1 amu during solar minimum to ˜2.8 amu during solar maximum. In such a case, the Alfvén velocity during solar maximum decreases to ˜60% of the solar minimum value. Thus, physical processes in the plasma sheet are considered to be much different between solar minimum and solar maximum. We also compared long-term variation of the plasma sheet ion composition with that of the substorm occurrence rate, which is evaluated by the number of Pi2 pulsations. No correlation or negative correlation was found between them. This result contradicts the O+ triggering substorm model, in which heavy ions in the plasma sheet increase the growth rate of the linear ion tearing mode and play an important role in localization and initiation of substorms. In contrast, O+ ions in the plasma sheet may prevent occurrence of substorms.

Enhanced Laser Cooling of Rare-Earth-Ion-Doped Composite Material

International Nuclear Information System (INIS)

You-Hua, Jia; Biao, Zhong; Xian-Ming, Ji; Jian-Ping, Yin

2008-01-01

We predict enhanced laser cooling performance of rare-earth-ions-doped glasses containing nanometre-sized ul-traBne particles, which can be achieved by the enhancement of local Geld around rare earth ions, owing to the surface plasma resonance of small metallic particles. The influence of energy transfer between ions and the particle is theoretically discussed. Depending on the particle size and the ion emission quantum efficiency, the enhancement of the absorption is predicted. It is concluded that the absorption are greatly enhanced in these composite materials, the cooling power is increased as compared to the bulk material

Heavy ion fusion- Using heavy ions to make electricity

International Nuclear Information System (INIS)

Celata, C.M.

2004-01-01

The idea of using nuclear fusion as a source of commercial electrical power has been pursued worldwide since the 1950s. Two approaches, using magnetic and inertial confinement of the reactants, are under study. This paper describes the difference between the two approaches, and discusses in more detail the heavy-ion-driven inertial fusion concept. A multibeam induction linear accelerator would be used to bring ∼100 heavy ion beams to a few GeV. The beams would then heat and compress a target of solid D-T. This approach is unique among fusion concepts in its ability to protect the reaction chamber wall from neutrons and debris

Novel high explosive compositions

Science.gov (United States)

Perry, D.D.; Fein, M.M.; Schoenfelder, C.W.

1968-04-16

This is a technique of preparing explosive compositions by the in-situ reaction of polynitroaliphatic compounds with one or more carboranes or carborane derivatives. One or more polynitroaliphatic reactants are combined with one or more carborane reactants in a suitable container and mixed to a homogeneous reaction mixture using a stream of inert gas or conventional mixing means. Ordinarily the container is a fissure, crack, or crevice in which the explosive is to be implanted. The ratio of reactants will determine not only the stoichiometry of the system, but will effect the quality and quantity of combustion products, the explosive force obtained as well as the impact sensitivity. The test values can shift with even relatively slight changes or modifications in the reaction conditions. Eighteen illustrative examples accompany the disclosure. (46 claims)

The Effects of Changing Membrane Compositions and Internal Electrolytes on the Respon of Potassium Ion Sensor

OpenAIRE

Ulianas, Alizar; Heng, Lee Yook

2015-01-01

A study on the changing of membrane compositions and internal solution towards the response potassium ion sensor was carried out. Potassium ion sensor based on photocured cross linking poly(n-butyl acrylate) membranes with varying composition of valinomycin (val), sodium tetrakis [3.5-bis(trifluoro-methyl) phenyl] borat (NaTFPB), types ion of internal solution were investigated. Effects of varying composition of val, NaTFPB, types and concentration of internal solution were observed on potass...

Tuning of wettability of PANI-GNP composites using keV energy ions

Energy Technology Data Exchange (ETDEWEB)

Lakshmi, G.B.V.S., E-mail: lakshmigbvs@gmail.com [Inter University Accelerator Centre, New Delhi 67 (India); Avasthi, D.K. [Amity University, Noida 201313, Uttar Pradesh (India)

2016-07-15

Polyaniline nanofiber composites with various nanomaterials have several applications in electrochemical biosensors. The surface properties of these composites coated electrodes play crucial role in enzyme absorption and analyte detection process. In the present study, Polyaniline-Graphene nanopowder (PANI-GNP) composites were prepared by rapid-mixing polymerization method. The films were prepared on ITO coated glass substrates and irradiated with 42 keV He{sup +} ions produced by indigenously fabricated accelerator at IUAC, New Delhi. The films were characterized before and after irradiation by SEM, Raman spectroscopy and contact angle measurements. The as-prepared films show superhydrophilic nature and after irradiation the films show highly hydrophobic nature with water contact angle (135°). The surface morphology was studied by SEM and structural changes were studied by Raman spectra. The surface morphological modifications induced by keV energy ions helps in tuning the wettability at different ion fluences.

Development of composite ion exchangers and their use in treatment of liquid radioactive wastes

International Nuclear Information System (INIS)

Sebesta, F.; John, J.; Motl, A.

1997-01-01

Composite inorganic-organic absorbers represent a group of inorganic ion exchangers modified by using binding organic material for preparation of larger size particles having higher granular strength. Such modification of originally powdered or microcrystalline inorganic ion exchangers makes their application in packed beds possible. Modified polyacrylonitrile (PAN) has been used as a universal binding polymer for a number of inorganic ion exchangers. The kinetics of ion exchange and sorption capacity of such composite absorbers is not influenced by the binding polymer mentioned above. The contents of active component in composite absorber can be varied over a very broad range (5-95% of the dry weight of the composite absorber). These composite absorbers have been tested for separation and concentration of various contaminants from aqueous solutions. Their high selectivity and sorption efficiency are advantageous for treatment of various radioactive and/or industrial waste waters, removal of natural and/or artificial radionuclides and heavy or toxic metals from underground water, determination of radionuclides ( 137 Cs, 60 Co, U, Ra) in the environment, etc. Examples of some of these applications are presented in this report. (author). 21 refs, 9 figs, 10 tabs

Renewable and superior thermal-resistant cellulose-based composite nonwoven as lithium-ion battery separator.

Science.gov (United States)

Zhang, Jianjun; Liu, Zhihong; Kong, Qingshan; Zhang, Chuanjian; Pang, Shuping; Yue, Liping; Wang, Xuejiang; Yao, Jianhua; Cui, Guanglei

2013-01-01

A renewable and superior thermal-resistant cellulose-based composite nonwoven was explored as lithium-ion battery separator via an electrospinning technique followed by a dip-coating process. It was demonstrated that such nanofibrous composite nonwoven possessed good electrolyte wettability, excellent heat tolerance, and high ionic conductivity. The cells using the composite separator displayed better rate capability and enhanced capacity retention, when compared to those of commercialized polypropylene separator under the same conditions. These fascinating characteristics would endow this renewable composite nonwoven a promising separator for high-power lithium-ion battery.

Origin of energetic ions in the polar cusp inferred from ion composition measurements by the Viking satellite

Directory of Open Access Journals (Sweden)

G. Kremser

Full Text Available The magnetospheric ion composition spectrometer MICS on the Swedish Viking satellite provided measurements of the ion composition in the energy range 10.1 keV/eleqE/Qleq326.0 keV/e. Data obtained during orbit 842 were used to investigate the ion distribution in the northern polar cusp and its vicinity. The satellite traversed the outer ring current, boundary region, cusp proper and plasma mantle during its poleward movement. H⁺ and He⁺⁺ ions were encountered in all of these regions. He⁺ ions were present only in the ring current. The number of O⁺ and O⁺⁺ ions was very small. Heavy high-charge state ions typical for the solar wind were observed for the first time, most of them in the poleward part of the boundary region and in the cusp proper. The H⁺ ions exhibited two periods with high intensities. One of them, called the BR/CP event, appeared at energies up to 50 keV. It started at the equatorward limit of the boundary region and continued into the cusp proper. Energy spectra indicate a ring current origin for the BR/CP event. Pitch angle distributions show downward streaming of H⁺ ions at its equatorward limit and upward streaming on the poleward side. This event is interpreted as the result of pitch angle scattering of ring current ions by fluctuations in the magnetopause current layer in combination with poleward convection. The other of the two periods with high H⁺ ion intensities, called the accelerated ion event, was superimposed on the BR/CP event. It was restricted to energies leq15 keV and occurred in the poleward part of the boundary region. This event is regarded as the high-energy tail of magnetosheath ions that were accelerated while penetrating into the magnetosphere. The cusp region thus contains ions of magnetospheric as well as of magnetosheath origin. The appearance of the ions depends, in addition to the ion source, on the

Adsorption behaviour and kinetics of exchange of Zn2+ and Eu3+ ions on a composite ion exchanger

International Nuclear Information System (INIS)

Morcos, T.N.

2007-01-01

Equilibria and kinetics of exchange of both Zn2+ and Eu3+ ions on a composite ion-exchanger, cobalt hexacyanocobaltate (III) (CoHCC) incorporated in polyacrylonitrile (PAN), has been studied. The apparent capacity of CoHCC-PAN for Zn2+ and Eu3+ was determined and found to be 0.353 and 0.69 meq/g, respectively. The higher capacity for Eu3+ ions than that for Zn2+ ions is due to the higher electrostatic interaction strength of the higher charge ion with the surface. Freundlich and Langmiur adsorption isotherms were used to investigate solute (Zn2+ or Eu3+) exchange phenomenon at the liquid/solid interface. The results indicated that both Langmuir and Freundlich isotherms fit well for both Zn2+ and Eu3+. Sorption data have been also treated with the Dubinin-Radushkevich equation. The kinetics of Zn2+ or Eu3+ sorption on the composite seems to show that the reaction was proceed via two steps. The first one was fast and probably due to adsorption followed by a slow exchange reaction. In view of the data obtained on the effect of particle size and metal ion concentrations on the rate of exchange reaction, it is concluded that the mechanism for both ions was chemical control. Generally, it seems that there are two exchange sites chemically equivalent but present in pores of different sizes which lead to different degrees of dehydration of the ions sorbed on the two sites

A Regime Diagram for Autoignition of Homogeneous Reactant Mixtures with Turbulent Velocity and Temperature Fluctuations

KAUST Repository

Im, Hong G.

2015-04-02

A theoretical scaling analysis is conducted to propose a diagram to predict weak and strong ignition regimes for a compositionally homogeneous reactant mixture with turbulent velocity and temperature fluctuations. The diagram provides guidance on expected ignition behavior based on the thermo-chemical properties of the mixture and the flow/scalar field conditions. The analysis is an extension of the original Zeldovich’s analysis by combining the turbulent flow and scalar characteristics in terms of the characteristic Damköhler and Reynolds numbers of the system, thereby providing unified and comprehensive understanding of the physical and chemical mechanisms controlling ignition characteristics. Estimated parameters for existing experimental measurements in a rapid compression facility show that the regime diagram predicts the observed ignition characteristics with good fidelity.

A Regime Diagram for Autoignition of Homogeneous Reactant Mixtures with Turbulent Velocity and Temperature Fluctuations

KAUST Repository

Im, Hong G.; Pal, Pinaki; Wooldridge, Margaret S.; Mansfield, Andrew B.

2015-01-01

A theoretical scaling analysis is conducted to propose a diagram to predict weak and strong ignition regimes for a compositionally homogeneous reactant mixture with turbulent velocity and temperature fluctuations. The diagram provides guidance on expected ignition behavior based on the thermo-chemical properties of the mixture and the flow/scalar field conditions. The analysis is an extension of the original Zeldovich’s analysis by combining the turbulent flow and scalar characteristics in terms of the characteristic Damköhler and Reynolds numbers of the system, thereby providing unified and comprehensive understanding of the physical and chemical mechanisms controlling ignition characteristics. Estimated parameters for existing experimental measurements in a rapid compression facility show that the regime diagram predicts the observed ignition characteristics with good fidelity.

The effects of combined therapy of rheumatoid arthritis on the acute phase reactants.

Science.gov (United States)

Rexhepi, Sylejman; Rexhepi, Mjellma; Sahatçiu-Meka, Vjollca; Pllana, Ejup; Dragusha, Gani; Gashi, Masar; Rexhepi, Blerta

2009-01-01

The paper presents the results of studies of acute phase reactants in the 60 treated patients with rheumatoid arthritis. Patients were divided into two groups, depending on the applied treatment: group I (n = 30) was treated with methotrexate, sulfasalazine and hydroxychloroquine, and group II (n = 30) with methotrexate. The results of our study shows that there is a statistically significant reduction in the value of acute phase reactants and clinical parameters after treatment in both investigated groups of patients, and also a significant statistical difference between the first and second group of treated patients.

MnO-carbon hybrid nanofiber composites as superior anode materials for lithium-ion batteries

International Nuclear Information System (INIS)

Wang, Jian-Gan; Yang, Ying; Huang, Zheng-Hong; Kang, Feiyu

2015-01-01

MnO-carbon hybrid nanofiber composites are fabricated by electrospinning polyimide/manganese acetylacetonate precursor and a subsequent carbonization process. The composition, phase structure and morphology of the composites are characterized by scanning and transmission electron microscopy, X-ray diffraction and thermogravimetric analysis. The results indicate that the composites exhibit good nanofibrous morphology with MnO nanoparticles uniformly encapsulated by carbon nanofibers. The hybrid nanofiber composites are used directly as freestanding anodes for lithium-ion batteries to evaluate their electrochemical properties. It is found that the optimized MnO-carbon nanofiber composite can deliver a high reversible capacity of 663 mAh g −1 , along with excellent cycling stability and good rate capability. The superior performance enables the composites to be promising candidates as an anode alternative for high-performance lithium-ion batteries

Heavy ion composition in the inner heliosphere: Predictions for Solar Orbiter

Science.gov (United States)

Lepri, S. T.; Livi, S. A.; Galvin, A. B.; Kistler, L. M.; Raines, J. M.; Allegrini, F.; Collier, M. R.; Zurbuchen, T.

2014-12-01

The Heavy Ion Sensor (HIS) on SO, with its high time resolution, will provide the first ever solar wind and surpathermal heavy ion composition and 3D velocity distribution function measurements inside the orbit of Mercury. These measurements will provide us the most in depth examination of the origin, structure and evolution of the solar wind. The near co-rotation phases of the orbiter will enable the most accurate mapping of in-situ structures back to their solar sources. Measurements of solar wind composition and heavy ion kinetic properties enable characterization of the sources, transport mechanisms and acceleration processes of the solar wind. This presentation will focus on the current state of in-situ studies of heavy ions in the solar wind and their implications for the sources of the solar wind, the nature of structure and variability in the solar wind, and the acceleration of particles. Additionally, we will also discuss opportunities for coordinated measurements across the payloads of Solar Orbiter and Solar Probe in order to answer key outstanding science questions of central interest to the Solar and Heliophysics communities.

The behavior of exciplex decay processes and interplay of radiationless transition and preliminary reorganization mechanisms of electron transfer in loose and tight pairs of reactants.

Science.gov (United States)

Kuzmin, Michael G; Soboleva, Irina V; Dolotova, Elena V

2007-01-18

Exciplex emission spectra and rate constants of their decay via internal conversion and intersystem crossing are studied and discussed in terms of conventional radiationless transition approach. Exciplexes of 9-cyanophenanthrene with 1,2,3-trimethoxybenzene and 1,3,5-trimethoxybenzene were studied in heptane, toluene, butyl acetate, dichloromethane, butyronitrile, and acetonitrile. A better description of spectra and rate constants is obtained using 0-0 transition energy and Gauss broadening of vibrational bands rather than the free energy of electron transfer and reorganization energy. The coincidence of parameters describing exciplex emission spectra and dependence of exciplex decay rate constants on energy gap gives the evidence of radiationless quantum transition mechanism rather than thermally activated medium reorganization mechanism of charge recombination in exciplexes and excited charge transfer complexes (contact radical ion pairs) as well as in solvent separated radical ion pairs. Radiationless quantum transition mechanism is shown to provide an appropriate description also for the main features of exergonic excited-state charge separation reactions if fast mutual transformations of loose and tight pairs of reactants are considered. In particular, very fast electron transfer (ET) in tight pairs of reactants with strong electronic coupling of locally excited and charge transfer states can prevent the observation of an inverted region in bimolecular excited-state charge separation even for highly exergonic reactions.

Alumina/Phenolphthalein Polyetherketone Ceramic Composite Polypropylene Separator Film for Lithium Ion Power Batteries

International Nuclear Information System (INIS)

Wang, Jing; Hu, Zhiyu; Yin, Xiunan; Li, Yunchao; Huo, Hong; Zhou, Jianjun; Li, Lin

2015-01-01

Highlights: • PEK-C (T g : ∼230 °C) was used as binder to prepare ceramic coated composite PP separator. • The composite PP separator was stable and showed low thermal shrinkage in the electrolyte solvent. • The composite PP separator was helpful for high current density discharge. • The composite PP separator improved the safety performance of the coin cells. - Abstract: One way to obtain the lithium ion power battery with better safety performance was to increase the thermal shrinkage resistance of the separator at higher temperature. Phenolphthalein polyetherketone (PEK-C) is a polymer that can withstand high temperature to about 230 °C. Here, we developed a new Al 2 O 3 coated composite polypropylene (PP) separator with PEK-C as binder. The coating layer was formed on the surface of the PP separator and both ceramic particles and binder did not infiltrated into the separator along the thickness direction. The composite separator with 4 μm coating layer provided balanced permeability and thermal shrinkage properties. The composite separator was stable at the electrochemical window for lithium ion battery. The coin cells with composite separator showed better charge/discharge performance than that of the cells with the PP separator. It seemed that the composite separator was helpful for high current density discharge. Also, the battery safety performance test had verified that the Al 2 O 3 coated composite separator with PEK-C as binder had truly improved the safety performance of the coin cells. So, the newly developed Al 2 O 3 coated composite PP separator was a promising safety product for lithium ion power batteries with high energy density

The composition of heavy ions in solar energetic particle events

International Nuclear Information System (INIS)

Fan, C.Y.

1984-01-01

The composition within individual SEP events may vary both with time and energy, and will in general be different from that in other SEP events. Average values of relative abundances measured in a large number of SEP events, however, are found to be roughly energy independent in the proportional1 to proportional20 MeV per nucleon range, and show a systematic deviation from photospheric abundances which seems to be organized in terms of the first ionization potential of the ion. Direct measurements of the charge states of SEPs have revealed the surprisingly common presence of energetic He + along with heavy ions with typically coronal ionization states. High-resolution measurements of isotopic abundance ratios in a small number of SEP events show these to be consistent with the universal composition except for the puzzling overabundance of the SEP 22 Ne/ 20 Ne relative to this isotopes ratio in the solar wind. The broad spectrum of observed elemental abundance variations, which in their extreme result in composition anomalies characteristic of 3 He-rich, heavy-ion rich and carbon-poor SEP events, along with direct measurements of the ionization states of SEPs provide essential information on the physical characteristics of, and conditions in the source regions, as well as important constraints to possible models for SEP production. (orig./HM)

Phase selection controlled by sodium ions in the synthesis of FAU/LTA composite zeolite

Directory of Open Access Journals (Sweden)

Linyan Hu, Sujuan Xie, Qingxia Wang, Shenglin Liu and Longya Xu

2009-01-01

Full Text Available Zeolite faujasite (FAU, Linde type A (LTA and FAU/LTA composite have been synthesized using tetramethylammonium cation (TMA + as template, by adjusting only the concentration of Na + ions in the initial solution (1.00 Al2 O3 4.36 SiO2 : 2.39 (TMA2 O : β Na2 O : 249.00H2 O. Na + ions alter the phase composition of the product more than TMA+ or OH− ions. When Na2 O concentration [Na2 O] increases from 0.024 to 0.168, the product gradually changes from pure FAU to pure LTA via the formation of FAU/LTA composite with increasing LTA fraction. Interestingly, the induction periods of FAU and LTA in the FAU/LTA composite zeolite ([Na2 O] is 0.072 are both 13 h, quite different from the induction periods of their individual pure phases—45 h for FAU and 4 h for LTA. During the crystallization, the LTA/(FAU + LTA fraction in the composite zeolite decreases in a nearly linear fashion. Scanning electron microscopy, thermogravimetry and differential thermal analysis indicate some difference between the properties of the FAU/LTA composite zeolite and of the mechanical mixture.

A high-resolution mass spectrometer to measure atmospheric ion composition

Directory of Open Access Journals (Sweden)

H. Junninen

2010-08-01

Full Text Available In this paper we present recent achievements on developing and testing a tool to detect the composition of ambient ions in the mass/charge range up to 2000 Th. The instrument is an Atmospheric Pressure Interface Time-of-Flight Mass Spectrometer (APi-TOF, Tofwerk AG. Its mass accuracy is better than 0.002%, and the mass resolving power is 3000 Th/Th. In the data analysis, a new efficient Matlab based set of programs (tofTools were developed, tested and used. The APi-TOF was tested both in laboratory conditions and applied to outdoor air sampling in Helsinki at the SMEAR III station. Transmission efficiency calibrations showed a throughput of 0.1–0.5% in the range 100–1300 Th for positive ions, and linearity over 3 orders of magnitude in concentration was determined. In the laboratory tests the APi-TOF detected sulphuric acid-ammonia clusters in high concentration from a nebulised sample illustrating the potential of the instrument in revealing the role of sulphuric acid clusters in atmospheric new particle formation. The APi-TOF features a high enough accuracy, resolution and sensitivity for the determination of the composition of atmospheric small ions although the total concentration of those ions is typically only 400–2000 cm⁻³. The atmospheric ions were identified based on their exact masses, utilizing Kendrick analysis and correlograms as well as narrowing down the potential candidates based on their proton affinities as well isotopic patterns. In Helsinki during day-time the main negative ambient small ions were inorganic acids and their clusters. The positive ions were more complex, the main compounds were (polyalkyl pyridines and – amines. The APi-TOF provides a near universal interface for atmospheric pressure sampling, and this key feature will be utilized in future laboratory and field studies.

Molecular beam studies of ion-molecule reactions

International Nuclear Information System (INIS)

Gentry, W.R.

1978-01-01

A review is presented in which an attempt is made to highlight some of the areas in which molecular beam techniques contribute to the understanding of ion--molecule reaction dynamics. Included are reactant kinetic energy range and resolution, internal state selection and analysis, and new chemical systems and phenomena. 35 references

Synthesis, characterization and nitrite ion sensing performance of reclaimable composite samples through a core-shell structure

Science.gov (United States)

Cui, Xiao; Yuqing, Zhao; Cui, Jiantao; Zheng, Qian; Bo, Wang

2018-02-01

The following paper reported and discussed a nitrite ion optical sensing platform based on a core-shell structure, using superamagnetic nanoparticles as the core, a silica molecular sieve MCM-41 as the shell and two rhodamine derivatives as probe, respectively. This superamagnetic core made this sensing platform reclaimable after finishing nitrite ion sensing procedure. This sensing platform was carefully characterized by means of electron microscopy images, porous structure analysis, magnetic response, IR spectra and thermal stability analysis. Detailed analysis suggested that the emission of these composite samples was quenchable by nitrite ion, showing emission turn off effect. A static sensing mechanism based on an additive reaction between chemosensors and nitrite ion was proposed. These composite samples followed Demas quenching equation against different nitrite ion concentrations. Limit of detection value was obtained as low as 0.4 μM. It was found that, after being quenched by nitrite ion, these composite samples could be reclaimed and recovered by sulphamic acid, confirming their recyclability.

Boron oxide–tin oxide/graphene composite as anode materials for lithium ion batteries

International Nuclear Information System (INIS)

Wen, Lina; Qin, Xue; Meng, Wei; Cao, Ning; Song, Zhonghai

2016-01-01

Highlights: • B_2O_3–SnO_2/G anode material is prepared by chemical heat solvent method for LIBs. • B_2O_3–SnO_2/G shows much improved cycling performance and rate capability. • B_2O_3 plays an important role in improving the performance. - Abstract: B_2O_3–SnO_2/graphene (B_2O_3–SnO_2/G) composite is fabricated via a chemical heat solvent method and utilized as anode material for lithium ion batteries. The added B_2O_3 dramatically improves the electrochemical performance of lithium ion batteries compared to the SnO_2/G composite. The B_2O_3–SnO_2/G composites as anode show an outstanding discharge capacity of 1404.9 mAh g"−"1 at 500 mA g"−"1 after 200 cycles and an excellent rate capacity, which apparently outperforms the previously reported SnO_2-based anode material. These improved electrochemical performance characteristics are due to the B_2O_3 played a buffering role, which are easily beneficial for accommodating the volume change during the lithium ions insertion/extraction processes. Furthermore, boron atoms can accept electrons for its electron-deficient nature and boron ions could release electrons, which lead to electrons' increased density and conductivity are increased. The results indicate that the B_2O_3–SnO_2/G composite is a promising anode material for lithium ion batteries.

Preparation of Advanced CuO Nanowires/Functionalized Graphene Composite Anode Material for Lithium Ion Batteries

Directory of Open Access Journals (Sweden)

Jin Zhang

2017-01-01

Full Text Available The copper oxide (CuO nanowires/functionalized graphene (f-graphene composite material was successfully composed by a one-pot synthesis method. The f-graphene synthesized through the Birch reduction chemistry method was modified with functional group “–(CH25COOH”, and the CuO nanowires (NWs were well dispersed in the f-graphene sheets. When used as anode materials in lithium-ion batteries, the composite exhibited good cyclic stability and decent specific capacity of 677 mA·h·g−1 after 50 cycles. CuO NWs can enhance the lithium-ion storage of the composites while the f-graphene effectively resists the volume expansion of the CuO NWs during the galvanostatic charge/discharge cyclic process, and provide a conductive paths for charge transportation. The good electrochemical performance of the synthesized CuO/f-graphene composite suggests great potential of the composite materials for lithium-ion batteries anodes.

Magnetic composite beads for sorption of cesium ions from aqueous streams

International Nuclear Information System (INIS)

Shinde, Rakesh N.; Pandey, A.K.; Acharya, R.; Rajurkar, N.S.

2014-01-01

Magnetic separation of metal ions is one of the promising methods due to simple, fast, efficient and cost effective technology. Highly selective magnetic sorbents can be designed by immobilizing functional groups in magnetic carrier which binds to the target specific ions. In the present work chitosan-(3-aminopropyl) triethoxysilane (APTS)- copperferrocyanide (CFC) composite beads have been synthesized for sorption of 137 Cs ions from aqueous streams. Physical characterization of the best resulted polymer beads was carried out by SEM-EDX and VSM technique. Sorption of Cs ions in the various magnetic polymer beads were studied in different aqueous condition by 137 Cs (662 KeV) radiotracer assay

Acute-phase reactants in periodontal disease: current concepts and future implications.

Science.gov (United States)

Archana, Vilasan; Ambili, Ranjith; Nisha, Krishnavilasam Jayakumary; Seba, Abraham; Preeja, Chandran

2015-05-01

Periodontal disease has been linked to adverse cardiovascular events by unknown mechanisms. C-reactive protein is a systemic marker released during the acute phase of an inflammatory response and is a prognostic marker for cardiovascular disease, with elevated serum levels being reported during periodontal disease. Studies also reported elevated levels of various other acute-phase reactants in periodontal disease. It has been reported extensively in the literature that treatment of periodontal infections can significantly lower serum levels of C-reactive protein. Therefore, an understanding of the relationship between acute-phase response and the progression of periodontal disease and other systemic health complications would have a profound effect on the periodontal treatment strategies. In view of this fact, the present review highlights an overview of acute-phase reactants and their role in periodontal disease. © 2014 Wiley Publishing Asia Pty Ltd.

Carbon nanotube/carbon nanotube composite AFM probes prepared using ion flux molding

Science.gov (United States)

Chesmore, Grace; Roque, Carrollyn; Barber, Richard

The performance of carbon nanotube-carbon nanotube composite (CNT/CNT composite) atomic force microscopy (AFM) probes is compared to that of conventional Si probes in AFM tapping mode. The ion flux molding (IFM) process, aiming an ion beam at the CNT probe, aligns the tip to a desired angle. The result is a relatively rigid tip that is oriented to offset the cantilever angle. Scans using these probes reveal an improvement in image accuracy over conventional tips, while allowing higher aspect ratio imaging of 3D surface features. Furthermore, the lifetimes of CNT-CNT composite tips are observed to be longer than both conventional tips and those claimed for other CNT technologies. Novel applications include the imaging of embiid silk. Supported by the Clare Boothe Luce Research Scholars Award and Carbon Design Innovations.

A polymeric membrane ion selective electrode based on organic-inorganic composite ion exchanger for the determination of thorium(IV)

International Nuclear Information System (INIS)

Chandra, Sulekh; Agarwal, Himanshu; Chandan Kumar, Singh; Sindhu, Susheel Kumar; Pankaj Kumar

2005-01-01

A poly(vinyl chloride) membrane electrode based on organic- inorganic composite ion exchanger, tin(IV) tungstoselenate-pyridine, has been prepared and tested for the selective determination of thorium(IV) ions. The PVC membrane electrode comprising 16% composite ion exchanger as the electroactive phase, 50% o-dioctyl phthalate as plasticizer, 4% tetraphenyl borate as anionic excluder and 30% poly(vinylchloride) displays a linear response to thorium(IV) ions over a wide concentration range of 1.0 x 10 -1 -8.0 x 10 -6 M with a Nernstain slope of 14.2 mV/ decade. The electrode shows a very short response time (∼15 s) and may be used in the pH range 2.5-9.0. The selectivity coefficient for alkali, alkaline earth and transition is smaller than 4.0 x 10 -4 . The sensor has been successfully used as an indicator electrode in the potentiometric titration of Th 4+ with EDTA as well as also for the determination of Th 4+ in the binary mixtures. (author)

Integrated ion imprinted polymers-paper composites for selective and sensitive detection of Cd(II) ions

Energy Technology Data Exchange (ETDEWEB)

Huang, Kai [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China); Chen, Ying [Hubei Center for Disease Control and Prevention, No. 6 ZhuoDao Quan North Road, 430079, Wuhan (China); Zhou, Feng [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China); Zhao, Xiaoya [Hubei Entry-Exit Inspection and Quarantine Bureau of PRC, No.588 Qingtaidadao Road, Hubei, 430022, Wuhan (China); Liu, Jiafa [Hubei Center for Disease Control and Prevention, No. 6 ZhuoDao Quan North Road, 430079, Wuhan (China); Mei, Surong; Zhou, Yikai [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China); Jing, Tao, E-mail: jingtao@hust.edu.cn [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China)

2017-07-05

Highlights: • IIPs are first grafted on the low-cost A4 print paper to develop an integrated paper-based device. • As an imprinted composite, the adsorption capacity is 155.2 mg g{sup –1} and the imprinted factor is more than 3.0. • As an analytical method, the limit of detection is 0.4 ng mL{sup –1}. • Based on the water quality standards, it could be used to determine Cd(II) ions in drinking water. - Abstract: Paper-based sensor is a new alternative technology to develop a portable, low-cost, and rapid analysis system in environmental chemistry. In this study, ion imprinted polymers (IIPs) using cadmium ions as the template were directly grafted on the surface of low-cost print paper based on the reversible addition-fragmentation chain transfer polymerization. It can be applied as a recognition element to selectively capture the target ions in the complex samples. The maximum adsorption capacity of IIPs composites was 155.2 mg g{sup –1} and the imprinted factor was more than 3.0. Then, IIPs-paper platform could be also applied as a detection element for highly selective and sensitive detection of Cd(II) ions without complex sample pretreatment and expensive instrument, due to the selective recognition, formation of dithizone-cadmium complexes and light transmission ability. Under the optimized condition, the linear range was changed from 1 to 100 ng mL{sup –1} and the limit of detection was 0.4 ng mL{sup –1}. The results were in good agreement with the classic ICP-MS method. Furthermore, the proposed method can also be developed for detection of other heavy metals by designing of new IIPs.

Effect of ion composition on oblique magnetosonic waves

International Nuclear Information System (INIS)

Kondo, Yuichi; Toida, Mieko

2011-01-01

The effects of ion composition on oblique magnetosonic waves in a two-ion-species plasma are studied theoretically and numerically. First, it is analytically shown that the KdV equation for the low-frequency mode, the lower branch of magnetosonic waves, is valid for amplitudes ε max (l-) , where ε max (l-) is a measure of the upper limit of the amplitude of the rarefactive solitary pulse of the low-frequency mode and is given as a function of the propagation angle of the wave θ, the density ratio and cyclotron frequency ratio of two ion species. The value of ε max (l-) increases with decreasing θ. Next, with electromagnetic particle simulations, the nonlinear evolution of the low- and high-frequency modes is examined. It is demonstrated that shorter-wavelength low- and high-frequency-mode waves are generated from a long-wavelength low-frequency-mode pulse if its amplitude ε exceeds ε max (l-) . (author)

Changes in the composition of brain interstitial ions control the sleep-wake cycle

DEFF Research Database (Denmark)

Ding, Fengfei; O'Donnell, John; Xu, Qiwu

2016-01-01

, and [H+]e as well as the extracellular volume. Local cortical activity of sleeping mice could be readily converted to the stereotypical electroencephalography pattern of wakefulness by simply imposing a change in the extracellular ion composition. Thus, extracellular ions control the state...

Boron oxide–tin oxide/graphene composite as anode materials for lithium ion batteries

Energy Technology Data Exchange (ETDEWEB)

Wen, Lina [Department of chemistry, School of Science, Tianjin University, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072 (China); Qin, Xue, E-mail: qinxue@tju.edu.cn [Department of chemistry, School of Science, Tianjin University, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072 (China); Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), College of Chemistry, Nankai University, Tianjin 300071 (China); Meng, Wei; Cao, Ning; Song, Zhonghai [Department of chemistry, School of Science, Tianjin University, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072 (China)

2016-11-15

Highlights: • B{sub 2}O{sub 3}–SnO{sub 2}/G anode material is prepared by chemical heat solvent method for LIBs. • B{sub 2}O{sub 3}–SnO{sub 2}/G shows much improved cycling performance and rate capability. • B{sub 2}O{sub 3} plays an important role in improving the performance. - Abstract: B{sub 2}O{sub 3}–SnO{sub 2}/graphene (B{sub 2}O{sub 3}–SnO{sub 2}/G) composite is fabricated via a chemical heat solvent method and utilized as anode material for lithium ion batteries. The added B{sub 2}O{sub 3} dramatically improves the electrochemical performance of lithium ion batteries compared to the SnO{sub 2}/G composite. The B{sub 2}O{sub 3}–SnO{sub 2}/G composites as anode show an outstanding discharge capacity of 1404.9 mAh g{sup −1} at 500 mA g{sup −1} after 200 cycles and an excellent rate capacity, which apparently outperforms the previously reported SnO{sub 2}-based anode material. These improved electrochemical performance characteristics are due to the B{sub 2}O{sub 3} played a buffering role, which are easily beneficial for accommodating the volume change during the lithium ions insertion/extraction processes. Furthermore, boron atoms can accept electrons for its electron-deficient nature and boron ions could release electrons, which lead to electrons' increased density and conductivity are increased. The results indicate that the B{sub 2}O{sub 3}–SnO{sub 2}/G composite is a promising anode material for lithium ion batteries.

Ion beam analysis of PECVD silicon oxide thin films

International Nuclear Information System (INIS)

Fernandez-Lima, F.; Rodriguez, J.A.; Pedrero, E.; Fonseca Filho, H.D.; Llovera, A.; Riera, M.; Dominguez, C.; Behar, M.; Zawislak, F.C.

2006-01-01

A study of ion beam analysis techniques of plasma enhanced chemical vapor deposited (PECVD) silicon oxide thin films (1 μm thick) obtained from silane (SiH 4 ) and nitrous oxide (N 2 O) is reported. The film, elemental composition and surface morphology were determined as function of the reactant gas flow ratio, R = [N 2 O]/[SiH 4 ] in the 22-110 range using the Rutherford backscattering spectrometry, nuclear reaction analysis and atomic force microscopy techniques. The density of the films was determined by combining the RBS and thickness measurements. All the experiments were done at a deposition temperature of 300 deg. C. In all the cases almost stoichiometric oxides were obtained being the impurity content function of R. It was also observed that physical properties such as density, surface roughness and shape factor increase with R in the studied interval

Sponge-like reduced graphene oxide/silicon/carbon nanotube composites for lithium ion batteries

Science.gov (United States)

Fang, Menglu; Wang, Zhao; Chen, Xiaojun; Guan, Shiyou

2018-04-01

Three-dimensional sponge-like reduced graphene oxide/silicon/carbon nanotube composites were synthesized by one-step hydrothermal self-assembly using silicon nanoparticles, graphene oxide and amino modified carbon nanotubes to develop high-performance anode materials of lithium ion batteries. Scanning electron microscopy and transmission electron microscopy images show the structure of composites that Silicon nanoparticles are coated with reduced graphene oxide while amino modified carbon nanotubes wrap around the reduced graphene oxide in the composites. When applied to lithium ion battery, these composites exhibit high initial specific capacity of 2552 mA h/g at a current density of 0.05 A/g. In addition, reduced graphene oxide/silicon/carbon nanotube composites also have better cycle stability than bare Silicon nanoparticles electrode with the specific capacity of 1215 mA h/g after 100 cycles. The three-dimension sponge-like structure not only ensures the electrical conductivity but also buffers the huge volume change, which has broad potential application in the field of battery.

Composite sorbents of inorganic ion-exchangers and polyacrylonitrile binding matrix. Methods of modification of properties of inorganic ion-exchangers for application in column packed beds

International Nuclear Information System (INIS)

Sebesta, F.

1997-01-01

Methods of preparation of granules of inorganic ion exchangers as well as methods for improvement of granular strength of these materials are reviewed. The resulting ion exchangers are classified in three groups - 'intrinsic', supported and composite ion exchangers. Their properties are compared and possibilities of their technological application are evaluated. A new method of preparation of inorganic-organic composite sorbents of inorganic ion-exchangers and polyacrylonitrile binding matrix is described, advantages and disadvantages of such sorbents are discussed. Proposed fields of application include tratment of liquid radioactive and/or hazardous wastes, decontamination of natural water as well as analytical applications. (author)

Spatial atomic layer deposition for coating flexible porous Li-ion battery electrodes

Energy Technology Data Exchange (ETDEWEB)

Yersak, Alexander S.; Sharma, Kashish; Wallas, Jasmine M.; Dameron, Arrelaine A.; Li, Xuemin; Yang, Yongan; Hurst, Katherine E.; Ban, Chunmei; Tenent, Robert C.; George, Steven M. [Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309 and Department of Mechanical Engineering, University of Colorado, Boulder, Colorado 80309

2018-01-01

Ultrathin atomic layer deposition (ALD) coatings on the electrodes of Li-ion batteries can enhance the capacity stability of the Li-ion batteries. To commercialize ALD for Li-ion battery production, spatial ALD is needed to decrease coating times and provide a coating process compatible with continuous roll-to-roll (R2R) processing. The porous electrodes of Li-ion batteries provide a special challenge because higher reactant exposures are needed for spatial ALD in porous substrates. This work utilized a modular rotating cylinder spatial ALD reactor operating at rotation speeds up to 200 revolutions/min (RPM) and substrate speeds up to 200 m/min. The conditions for spatial ALD were adjusted to coat flexible porous substrates. The reactor was initially used to characterize spatial Al2O3 and ZnO ALD on flat, flexible metalized polyethylene terephthalate foils. These studies showed that slower rotation speeds and spacers between the precursor module and the two adjacent pumping modules could significantly increase the reactant exposure. The modular rotating cylinder reactor was then used to coat flexible, model porous anodic aluminum oxide (AAO) membranes. The uniformity of the ZnO ALD coatings on the porous AAO membranes was dependent on the aspect ratio of the pores and the reactant exposures. Larger reactant exposures led to better uniformity in the pores with higher aspect ratios. The reactant exposures were increased by adding spacers between the precursor module and the two adjacent pumping modules. The modular rotating cylinder reactor was also employed for Al2O3 ALD on porous LiCoO2 (LCO) battery electrodes. Uniform Al coverages were obtained using spacers between the precursor module and the two adjacent pumping modules at rotation speeds of 25 and 50 RPM. The LCO electrodes had a thickness of ~49 um and pores with aspect ratios of ~12-25. Coin cells were then constructed using the ALD-coated LCO electrodes and were tested to determine their battery

The GOES-16 Energetic Heavy Ion Sensor (EHIS) Ion Composition and Flux Measurements

Science.gov (United States)

Connell, J. J.; Lopate, C.

2017-12-01

The Energetic Heavy Ion Sensor (EHIS) was built by the University of New Hampshire, subcontracted to Assurance Technology Corporation, as part of the Space Environmental In-Situ Suite (SEISS) on the new GOES-16 satellite (formerly GOES-R) in Geostationary orbit. EHIS measures energetic ions over the range 10-200 MeV for protons, and energy ranges for heavy ions corresponding to the same stopping range (e.g., 19-207 MeV/u for carbon and 38-488 MeV/u for iron). EHIS uses the Angle Detecting Inclined Sensors (ADIS) technique to provide single-element charge resolution. Though on an operational mission for Space Weather monitoring, EHIS can thus provide a new source of high quality Solar Particle Event (SPE) data for science studies. With a high rate of on-board processing ( 2000 events/s), EHIS will provide exceptional statistics for ion composition measurements in large SPEs. For the GOES Level 1-B and Level 2 data products, heavy ions are distinguished in EHIS using pulse-height analysis with on-board processing producing charge histograms for five energy bands. Fits to these data are normalized to priority rate data on the ground. The instrumental cadence for histograms is 1 minute and the primary Level 1-B heavy ion data products are 1-minute and 5-minute averages. We discuss the preliminary EHIS heavy ion data results which show elemental peaks from H to Fe, with peaks for the isotopes D and 3He. (GOES-16 was launched in 19 November, 2016 and data has, though July 2017, been dominated by Galactic Cosmic Rays.) The EHIS instrument development project was funded by NASA under contract NNG06HX01C.

Technique for increasing dynamic range of space-borne ion composition instruments

International Nuclear Information System (INIS)

Burch, J.L.; Miller, G.P.; Santos, A. de los; Pollock, C.J.; Pope, S.E.; Valek, P. W.; Young, D.T.

2005-01-01

The dynamic range of ion composition spectrometers is limited by several factors, including saturation of particle counters and spillover of signals from highly dominant species into channels tuned to minor species. Instruments designed for composition measurements of hot plasmas in space can suffer greatly from both of these problems because of the wide energy range required and the wide disparity in fluxes encountered in various regions of interest. In order to detect minor ions in regions of very weak fluxes, geometry factors need to be as large as possible within the mass and volume resources available. As a result, problems with saturation by the dominant fluxes and spillover to minor-ion channels in plasma regions with intense fluxes become especially acute. This article reports on a technique for solving the dynamic-range problem in the few eV to several keV energy/charge range that is of central importance for space physics research where the dominant ion is of low mass/charge (typically H + ), and the minor ions are of higher mass/charge (typically O + ). The technique involves employing a radio-frequency modulation of the deflection electric field in the back section of an electrostatic analyzer in a time-of-flight instrument. This technique is shown to reduce H + counts by a controllable amount of up to factors of 1000 while reducing O + counts by only a few percent that can be calibrated

Composition dependent thermal annealing behaviour of ion tracks in apatite

Energy Technology Data Exchange (ETDEWEB)

Nadzri, A., E-mail: allina.nadzri@anu.edu.au [Department of Electronic Materials Engineering, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601 (Australia); Schauries, D.; Mota-Santiago, P.; Muradoglu, S. [Department of Electronic Materials Engineering, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601 (Australia); Trautmann, C. [GSI Helmholtz Centre for Heavy Ion Research, Planckstrasse 1, 64291 Darmstadt (Germany); Technische Universität Darmstadt, 64287 Darmstadt (Germany); Gleadow, A.J.W. [School of Earth Science, University of Melbourne, Melbourne, VIC 3010 (Australia); Hawley, A. [Australian Synchrotron, 800 Blackburn Road, Clayton, VIC 3168 (Australia); Kluth, P. [Department of Electronic Materials Engineering, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601 (Australia)

2016-07-15

Natural apatite samples with different F/Cl content from a variety of geological locations (Durango, Mexico; Mud Tank, Australia; and Snarum, Norway) were irradiated with swift heavy ions to simulate fission tracks. The annealing kinetics of the resulting ion tracks was investigated using synchrotron-based small-angle X-ray scattering (SAXS) combined with ex situ annealing. The activation energies for track recrystallization were extracted and consistent with previous studies using track-etching, tracks in the chlorine-rich Snarum apatite are more resistant to annealing than in the other compositions.

Electrolyte compositions for lithium ion batteries

Science.gov (United States)

Sun, Xiao-Guang; Dai, Sheng; Liao, Chen

2016-03-29

The invention is directed in a first aspect to an ionic liquid of the general formula Y.sup.+Z.sup.-, wherein Y.sup.+ is a positively-charged component of the ionic liquid and Z.sup.- is a negatively-charged component of the ionic liquid, wherein Z.sup.- is a boron-containing anion of the following formula: ##STR00001## The invention is also directed to electrolyte compositions in which the boron-containing ionic liquid Y.sup.+Z.sup.- is incorporated into a lithium ion battery electrolyte, with or without admixture with another ionic liquid Y.sup.+X.sup.- and/or non-ionic solvent and/or non-ionic solvent additive.

Adsorption of Cadmium Ions from Water on Double-walled Carbon Nanotubes/Iron Oxide Composite

Directory of Open Access Journals (Sweden)

Karima Seffah

2017-12-01

Full Text Available A new material (DWCNT/iron oxide for heavy metals removal was developed by combining the adsorption features of double-walled carbon nanotubes with the magnetic properties of iron oxides. Batch experiments were applied in order to evaluate adsorption capacity of the DWCNT/iron oxide composite for cadmium ions. The influence of operating parameters such as pH value, amount of adsorbent, initial adsorbate concentration and agitation speed was studied. The adsorption capacity of the DWCNT/iron oxide adsorbent for Cd2+ ions was 20.8 mg g-1, which is at the state of the art. The obtained results revealed that DWCNT/iron oxide composite is a very promising adsorbent for removal of Cd2+ ions from water under natural conditions. The advantage of the magnetic composite is that it can be used as adsorbent for contaminants in water and can be subsequently controlled and removed from the medium by a simple magnetic process.

Swift heavy ions induced surface modifications in Ag-polypyrrole composite films synthesized by an electrochemical route

International Nuclear Information System (INIS)

Kumar, Vijay; Ali, Yasir; Sharma, Kashma; Kumar, Vinod; Sonkawade, R.G.; Dhaliwal, A.S.; Swart, H.C.

2014-01-01

Highlights: • Two steps electrochemical synthesis for the fabrication of Ag-polypyrrole composite films. • Surface modifications by swift heavy ion beam. • SEM image shows the formation of craters and humps after irradiation. • Detailed structural analysis by Raman spectroscopy. - Abstract: The general aim of this work was to study the effects of swift heavy ions on the properties of electrochemically synthesized Ag-polypyrrole composite thin films. Initially, polypyrrole (PPy) films were electrochemically synthesized on indium tin oxide coated glass surfaces using a chronopotentiometery technique, at optimized process conditions. The prepared PPy films have functioned as working electrodes for the decoration of submicron Ag particles on the surface of the PPy films through a cyclicvoltammetry technique. Towards probing the effect of swift heavy ion irradiation on the structural and morphological properties, the composite films were subjected to a 40 MeV Li 3+ ion beam irradiation for various fluences (1 × 10 11 , 1 × 10 12 and 1 × 10 13 ions/cm 2 ). Comparative microstructural investigations were carried out after the different ion fluences using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy and micro-Raman spectroscopy techniques. Raman and SEM studies revealed that the structure of the films became disordered after irradiation. The SEM studies of irradiated composite films show significant changes in their surface morphologies. The surface was smoother at lower fluence but craters were observed at higher fluence

Swift heavy ions induced surface modifications in Ag-polypyrrole composite films synthesized by an electrochemical route

Energy Technology Data Exchange (ETDEWEB)

Kumar, Vijay, E-mail: vijays_phy@rediffmail.com [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa); Ali, Yasir [Department of Physics, Sant Longowal Institute of Engineering and Technology, Longowal, District Sangrur 148106, Punjab (India); Sharma, Kashma [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa); Department of Chemistry, Shoolini University of Biotechnology and Management Sciences, Solan 173212 (India); Kumar, Vinod [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa); Sonkawade, R.G. [Inter University Accelerator Center, Aruna Asif Ali Marg, New Delhi 110067 (India); Dhaliwal, A.S. [Department of Physics, Sant Longowal Institute of Engineering and Technology, Longowal, District Sangrur 148106, Punjab (India); Swart, H.C., E-mail: swarthc@ufs.ac.za [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA 9300 (South Africa)

2014-03-15

Highlights: • Two steps electrochemical synthesis for the fabrication of Ag-polypyrrole composite films. • Surface modifications by swift heavy ion beam. • SEM image shows the formation of craters and humps after irradiation. • Detailed structural analysis by Raman spectroscopy. - Abstract: The general aim of this work was to study the effects of swift heavy ions on the properties of electrochemically synthesized Ag-polypyrrole composite thin films. Initially, polypyrrole (PPy) films were electrochemically synthesized on indium tin oxide coated glass surfaces using a chronopotentiometery technique, at optimized process conditions. The prepared PPy films have functioned as working electrodes for the decoration of submicron Ag particles on the surface of the PPy films through a cyclicvoltammetry technique. Towards probing the effect of swift heavy ion irradiation on the structural and morphological properties, the composite films were subjected to a 40 MeV Li{sup 3+} ion beam irradiation for various fluences (1 × 10{sup 11}, 1 × 10{sup 12} and 1 × 10{sup 13} ions/cm{sup 2}). Comparative microstructural investigations were carried out after the different ion fluences using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy and micro-Raman spectroscopy techniques. Raman and SEM studies revealed that the structure of the films became disordered after irradiation. The SEM studies of irradiated composite films show significant changes in their surface morphologies. The surface was smoother at lower fluence but craters were observed at higher fluence.

Transesterification of castor oil usingMgO/SiO2 catalyst and coconutoilas co-reactant

OpenAIRE

Kamisah D. Pandiangan; Novesar Jamarun; Syukri Arief; Wasinton Simanjuntak

2016-01-01

This paper describes the transesterification of castor oil with the use of coconut oil as co-reactant and MgO/SiO2as heterogeneous base catalyst. The catalyst was preparedfrom rice husk silica and magnesium nitrate by sol-gel method, with MgO load of 20% relative to silica, and then subjected to sintering treatment at 600 oC for 6 hours. A series of experiments was carried out, indicating that the use of coconut oil as co-reactant significantly promoted the conversion of castor oil into b...

Fabrication of submicron structures in nanoparticle/polymer composite by holographic lithography and reactive ion etching

Science.gov (United States)

Zhang, A. Ping; He, Sailing; Kim, Kyoung Tae; Yoon, Yong-Kyu; Burzynski, Ryszard; Samoc, Marek; Prasad, Paras N.

2008-11-01

We report on the fabrication of nanoparticle/polymer submicron structures by combining holographic lithography and reactive ion etching. Silica nanoparticles are uniformly dispersed in a (SU8) polymer matrix at a high concentration, and in situ polymerization (cross-linking) is used to form a nanoparticle/polymer composite. Another photosensitive SU8 layer cast upon the nanoparticle/SU8 composite layer is structured through holographic lithography, whose pattern is finally transferred to the nanoparticle/SU8 layer by the reactive ion etching process. Honeycomb structures in a submicron scale are experimentally realized in the nanoparticle/SU8 composite.

Bulk-compositional changes of Ni2Al3 and NiAl3 during ion etching

International Nuclear Information System (INIS)

Chen Houwen; Wang Rong

2008-01-01

Bulk-compositional changes of Ni 2 Al 3 and NiAl 3 in a Ni-50 wt% Al alloy during ion etching have been investigated by transmission electron microscopy and energy dispersive X-ray spectroscopic analyses. After etching with 7, 5 and 3 keV Ar + ions for 15, 24 and 100 h nickel contents in both Ni 2 Al 3 and NiAl 3 exceeded greatly those in the initial compounds and increased with the decrement of the sputtering energy. After 100 h etching with 3 keV Ar + ions the compositions of these two compounds reached a similar value, about Ni 80-83 Al 12-15 Fe 3-4 Cr 1-2 (at%). A synergistic action of preferential sputtering, radiation-induced segregation and radiation-enhanced diffusion enables the altered-layers at the top and bottom of the film extend through the whole film. The bulk-compositional changes are proposed to occur in the unsteady-state sputtering regime of ion etching and caused by an insufficient supply of matter in a thin film

Mechanical properties of MeV ion-irradiated SiC/SiC composites characterized by indentation technique

International Nuclear Information System (INIS)

Park, J.Y.; Park, K.H.; Kim, W.; Kishimoto, H.; Kohyama, A.

2007-01-01

Full text of publication follows: SiC/SiC composites have been considered as a structural material for advanced fusion concepts. In the core of fusion reactor, those SiC/SiC composites are experienced the complex attacks such as strong neutron, high temperature and transmuted gases. One of the vital data for designing the SiC/SiC composites to the fusion reactor is mechanical properties under the severe neutron irradiation. In this work, various SiC/SiC composites were prepared by the different fabrication processes like CVI (chemical vapor infiltration), WA-CVI (SiC whisker assisted CVI) and hot-pressed method. The expected neutron irradiation was simulated by a silicon self-ion irradiation at a DuET facility; Dual-beam for Energy Technologies, Kyoto University. The irradiation temperature were 600 deg. C and 1200 deg. C, and the irradiation does were 5 dpa and 20 dpa, respectively. The 5.1 MeV Si ions were irradiated to the intrinsic CVI-SiC, SiC whisker reinforced SiC and SiC composites produced by hot-press method. The mechanical properties like hardness, elastic modulus and fracture toughness were characterized by an indentation technique. The ion irradiation caused the increase of the hardness and fracture toughness, which was dependent on the irradiation temperature. SiC whisker reinforcement in the SiC matrix accelerated the increase of the fracture toughness by the ion irradiation. For SiC/SiC composites after the ion irradiation, this work will provide the additional data for the mechanical properties as well as the effect of SiC whisker reinforcement. (authors)

Experimental composite guidance conduits for peripheral nerve repair: An evaluation of ion release

Energy Technology Data Exchange (ETDEWEB)

Zhang, X.F. [Department of Biological Sciences and Medical Engineering Design and Innovation Centre, Cork Institute of Technology, Cork (Ireland); Coughlan, A. [Inamori School of Engineering, Alfred University, Alfred, NY. 14802 (United States); O' Shea, H. [Department of Biological Sciences and Medical Engineering Design and Innovation Centre, Cork Institute of Technology, Cork (Ireland); Towler, M.R. [Inamori School of Engineering, Alfred University, Alfred, NY. 14802 (United States); Kehoe, S., E-mail: sharonkehoe@dal.ca [Department of Applied Oral Sciences, Dalhousie University, Halifax, NS, B3H 4R2 (Canada); School of Biomedical Engineering, Dalhousie University, Halifax, NS, B3H 4R2 (Canada); Boyd, D., E-mail: d.boyd@dal.ca [Department of Applied Oral Sciences, Dalhousie University, Halifax, NS, B3H 4R2 (Canada); School of Biomedical Engineering, Dalhousie University, Halifax, NS, B3H 4R2 (Canada)

2012-08-01

Poly (lactide-co-glycolide) (PLGA) - Pluronic F127 - glass composites have demonstrated excellent potential, from the perspective of controlled mechanical properties and cytocompatibility, for peripheral nerve regeneration. In addition to controlling the mechanical properties and cytotoxicity for such composite devices, the glass component may mediate specific responses upon implantation via degradation in the physiological environment and release of constituent elements. However, research focused on quantifying the release levels of such therapeutic ions from these experimental medical devices has been limited. To redress the balance, this paper explores the ion release profiles for Si{sup 4+}, Ca{sup 2+}, Na{sup +}, Zn{sup 2+}, and Ce{sup 4+} from experimental composite nerve guidance conduits (CNGC) comprising PLGA (at 12.5, and 20 wt.%), F127 (at 0, 2.5 and 5 wt.%) and various loadings of Si-Ca-Na-Zn-Ce glass (at 20 and 40 wt.%) for incubation periods of up to 28 days. The concentration of each ion, at various time points, was determined using Inductively Coupled Plasma-Atomic Emission Spectrometry (Perkin Elmer Optima 3000). It was observed that the Si{sup 4+}, Na{sup +}, Ca{sup 2+}, Zn{sup 2+} release from CNGCs in this study ranged from 0.22 to 6.477 ppm, 2.307 to 3.277 ppm, 40 to 119 ppm, and 45 to 51 ppm, respectively. The Ce{sup 4+} concentrations were under the minimum detection limits for the ICP instrument utilized. The results indicate that the ion release levels may be appropriate to mediate therapeutic effects with respect to peripheral nerve regeneration. The data generated in this paper provides requisite evidence to optimize composition for pre-clinical evaluation of the experimental composite. - Graphical abstract: Highlights: Black-Right-Pointing-Pointer Time-dependent degradation studies of PLGA/glass composite nerve guidance conduits (NGCs). Black-Right-Pointing-Pointer Si{sup 4+}, Na{sup +}, Ca{sup 2+} and Zn{sup 2+} release levels for the

Kinetics and equilibrium studies for sorption of Cu (II) and Cr (VI) ions onto polymeric composite resins

International Nuclear Information System (INIS)

El-Zahhhar, A.A.; Abdel-Aziz, H.M.; Siyam, T.

2005-01-01

The sorption behavior of Cu (II) and Cr (VI) ions from aqueous solutions was studied using polymeric composite resins. Batch sorption experiments were performed as a function of hydrogen ion concentration, complexing agent concentration, resin weight and ionic strength. Kinetic parameters as a function of initial ion concentration were determined to predict the sorption behavior of Cu (II) and Cr (VI) onto polymeric composite resins. The equilibrium data could be fitted by the frendlich adsorption isotherm equation

Combustion synthesis of boride and other composites

International Nuclear Information System (INIS)

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

1989-01-01

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

Possible mechanisms for the interaction of polymeric composite resins with Cu(II) ions in aqueous solution

International Nuclear Information System (INIS)

El-Zahhhar, A.A.; Abdel-Aziz, H.M.; Siyam, T.

2005-01-01

The interaction between the active groups of polymeric composite resins such as Poly(acrylamide-acrylic acid)-ethylenediaminetetra acetic acid disodium salt P(AM-AA)EDTANa 2 , Poly(acrylamide-acrylic acid)- montmorillonite P(AM-AA)-montmorillonite, and Poly(acrylamide-acrylic acid)-potassium nickel hexacyanoferrate P(AM-AA)-KNiHCF, with copper sulfate as a test ion has been studied. The spectroscopic studies show that the mechanism of interaction between polymeric composite resins and copper sulfate is a bond formation between the active groups of polymeric chains and copper ion. The bond formation depends on nature of polymeric chains. It was also found that the amide groups form complexes with hydrated cations, while carboxylate group interact by ion exchange mechanism through complex formation. Montmorillonite and hexacyanoferrate of the resins interact with metal ions by ion exchange mechanism

Effect of elemental composition of ion beam on the phase formation and surface strengthening of structural materials

International Nuclear Information System (INIS)

Avdienko, K.I.; Avdienko, A.A.; Kovalenko, I.A.

2001-01-01

The investigation results are reported on the influence of ion beam element composition on phase formation, wear resistance and microhardness of surface layers of titanium alloys VT-4 and VT-16 as well as stainless steel 12Kh18N10T implanted with nitrogen, oxygen and boron. It is stated that ion implantation into structural materials results in surface hardening and is directly dependent on element composition of implanted ion beam. The presence of oxygen in boron or nitrogen ion beams prevents the formation of boride and nitride phases thus decreasing a hardening effect [ru

Synthesis of nanoparticles from malleable and ductile metals using powder-free, reactant-assisted mechanical attrition.

Science.gov (United States)

McMahon, Brandon W; Perez, Jesus Paulo L; Yu, Jiang; Boatz, Jerry A; Anderson, Scott L

2014-11-26

A reactant-assisted mechanochemical method was used to produce copious nanoparticles from malleable/ductile metals, demonstrated here for aluminum, iron, and copper. The milling media is intentionally degraded via a reactant-accelerated wear process, where the reactant aids particle production by binding to the metal surfaces, enhancing particle production, and reducing the tendency toward mechanochemical (cold) welding. The mechanism is explored by comparing the effects of different types of solvents and solvent mixtures on the amount and type of particles produced. Particles were functionalized with oleic acid to aid in particle size separation, enhance dispersion in hydrocarbon solvents, and protect the particles from oxidation. For aluminum and iron, the result is air-stable particles, but for copper, the suspended particles are found to dissolve when exposed to air. Characterization was performed using electron microscopy, dynamic light scattering, Fourier transform infrared spectroscopy, solid state nuclear magnetic resonance, and X-ray photoelectron spectroscopy. Density functional theory was used to examine the nature of carboxylic acid binding to the aluminum surface, confirming the dominance of bridging bidentate binding.

Removal of Heavy Metal Ions by Using Composite of Cement Kiln Dust/Ethylene Glycol co Acrylic Acid Prepared by y-Irradiation

International Nuclear Information System (INIS)

Sokker, H.H.; Abdel-Rahman, H.A.; Khattab, M.M.; Ismail, M.R.

2010-01-01

Various composites of cement kiln dust (CKD) and poly(ethylene glycol co acrylic acid) using y-irradiation was investigated. The samples were prepared using three percentages of cement kiln dust namely, 20, 50 and 75 by wt % and mixed with an equimolar ratio (1:1) of ethylene glycol and acrylic acid then irradiated at doses; 10,20 and 30 kGy of gamma-irradiation. The results showed that (CKD) and poly(ethylene glycol co acrylic acid) composites were formed only at 30 kGy. In addition, CKD alone has the lowest degree of removal of heavy metal ions compared with the prepared composites. A composite containing 75% cement kiln dust by weight percentage, showed the highest degree of removal of cobalt ions, whereas, a composite of 20% CKD showed the highest degree for cadmium ion removal. While the composite of 75% CKD showed a higher selectivity of cobalt ion than cadmium ion in their mixed solution.

Highly efficient quenching of tris(2,2'-bipyridyl)ruthenium(II) electrochemiluminescence by ozone using formaldehyde, methylglyoxal, and glyoxalate as co-reactants and its application to ozone sensing.

Science.gov (United States)

Gao, Ying; Liu, Xiaoyun; Qi, Wenjing; Gao, Wenyue; Li, Yunhui; Xu, Guobao

2015-06-21

Most electrochemiluminescence (ECL) systems require high concentrations of quencher to totally quench ECL. In this study, we found that ozone can quench tris(2,2'-bipyridyl)ruthenium(II) ECL using formaldehyde, methylglyoxal, or glyoxalate as co-reactants at a glassy carbon electrode with remarkable efficiencies even when the concentration of ozone is merely 0.25% of that of the co-reactant. The strongest quenching is observed with the tris(2,2'-bipyridyl)ruthenium(II)/formaldehyde ECL system. The tris(2,2'-bipyridyl)ruthenium(II)/formaldehyde ECL intensities decrease linearly with the ozone concentration over the range of 0.025-25 μM (r = 0.9947) with a limit of detection of 8 nM. The method is more sensitive and faster than most methods. It shows high selectivity in the presence of other ROS or oxidants and some metal ions, such as H2O2, ClO(-), Mg(2+), Ni(2+), etc. The method exhibits high recoveries for the detection of ozone in a ventilated photocopy room.

A Simple Analytical Model for Predicting the Detectable Ion Current in Ion Mobility Spectrometry Using Corona Discharge Ionization Sources

Science.gov (United States)

Kirk, Ansgar Thomas; Kobelt, Tim; Spehlbrink, Hauke; Zimmermann, Stefan

2018-05-01

Corona discharge ionization sources are often used in ion mobility spectrometers (IMS) when a non-radioactive ion source with high ion currents is required. Typically, the corona discharge is followed by a reaction region where analyte ions are formed from the reactant ions. In this work, we present a simple yet sufficiently accurate model for predicting the ion current available at the end of this reaction region when operating at reduced pressure as in High Kinetic Energy Ion Mobility Spectrometers (HiKE-IMS) or most IMS-MS instruments. It yields excellent qualitative agreement with measurement results and is even able to calculate the ion current within an error of 15%. Additional interesting findings of this model are the ion current at the end of the reaction region being independent from the ion current generated by the corona discharge and the ion current in High Kinetic Energy Ion Mobility Spectrometers (HiKE-IMS) growing quadratically when scaling down the length of the reaction region. [Figure not available: see fulltext.

Correlation of shear and dielectric ion viscosity of dental resins - Influence of composition, temperature and filler content.

Science.gov (United States)

Steinhaus, Johannes; Hausnerova, Berenika; Haenel, Thomas; Selig, Daniela; Duvenbeck, Fabian; Moeginger, Bernhard

2016-07-01

Shear viscosity and ion viscosity of uncured visible light-curing (VLC) resins and resin based composites (RBC) are correlated with respect to the resin composition, temperature and filler content to check where Dielectric Analysis (DEA) investigations of VLC RBC generate similar results as viscosity measurements. Mixtures of bisphenol A glycidyl methacrylate (Bis-GMA) and triethylene glycol dimethacrylate (TEGDMA) as well as the pure resins were investigated and compared with two commercial VLC dental resins and RBCs (VOCO, Arabesk Top and Grandio). Shear viscosity data was obtained using a Haake Mars III, Thermo Scientific. Ion viscosity measurements performed by a dielectric cure analyzer (DEA 231/1 Epsilon with Mini IDEX-Sensor, Netzsch-Gerätebau). Shear viscosity depends reciprocally on the mobility of molecules, whereas the ion viscosity also depends on the ion concentration as it is affected by both ion concentration and mixture viscosity. Except of pure TEGDMA, shear and ion viscosities depend on the resin composition qualitatively in a similar manner. Furthermore, shear and ion viscosities of the commercial VLC dental resins and composites exhibited the same temperature dependency regardless of filler content. Application of typical rheological models (Kitano and Quemada) revealed that ion viscosity measurements can be described with respect to filler contents of up to 30vol.%. Rheological behavior of a VLC RBC can be characterized by DEA under the condition that the ion concentration is kept constant. Both methods address the same physical phenomenon - motion of molecules. The proposed relations allows for calculating the viscosity of any Bis-GMA-TEGDMA mixture on the base of the viscosities of the pure components. This study demonstrated the applicability of DEA investigations of VLC RBCs with respect to quality assurance purposes. Copyright © 2016 The Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

Simulation studies of acceleration of heavy ions and their elemental compositions

International Nuclear Information System (INIS)

Toida, Mieko; Ohsawa, Yukiharu

1996-07-01

By using a one-dimensional, electromagnetic particle simulation code with full ion and electron dynamics, we have studied the acceleration of heavy ions by a nonlinear magnetosonic wave in a multi-ion-species plasma. First, we describe the mechanism of heavy ion acceleration by magnetosonic waves. We then investigate this by particle simulations. The simulation plasma contains four ion species: H, He, O, and Fe. The number density of He is taken to be 10% of that of H, and those of O and Fe are much lower. Simulations confirm that, as in a single-ion-species plasma, some of the hydrogens can be accelerated by the longitudinal electric field formed in the wave. Furthermore, they show that magnetosonic waves can accelerate all the particles of all the heavy species (He, O, and Fe) by a different mechanism, i.e., by the transverse electric field. The maximum speeds of the heavy species are about the same, of the order of the wave propagation speed. These are in good agreement with theoretical prediction. These results indicate that, if high-energy ions are produced in the solar corona through these mechanisms, the elemental compositions of these heavy ions can be similar to that of the background plasma, i.e., the corona

Composition and temporal behavior of ambient ions in the boreal forest

Directory of Open Access Journals (Sweden)

M. Ehn

2010-09-01

Full Text Available A recently developed atmospheric pressure interface mass spectrometer (APi-TOF measured the negative and positive ambient ion composition at a boreal forest site. As observed in previous studies, the negative ions were dominated by strong organic and inorganic acids (e.g. malonic, nitric and sulfuric acid, whereas the positive ions consisted of strong bases (e.g. alkyl pyridines and quinolines. Several new ions and clusters of ions were identified based on their exact masses, made possible by the high resolution, mass accuracy and sensitivity of the APi-TOF. Time series correlograms aided in peak identification and assigning the atomic compositions to molecules. Quantum chemical calculations of proton affinities and cluster stabilities were also used to confirm the plausibility of the assignments. Acids in the gas phase are predominantly formed by oxidation in the gas phase, and thus the concentrations are expected to vary strongly between day and night. This was also the case in this study, where the negative ions showed strong diurnal behavior, whereas the daily changes in the positive ions were considerably smaller. A special focus in this work was the changes in the ion distributions occurring during new particle formation events. We found that sulfuric acid, together with its clusters, dominated the negative ion spectrum during these events. The monomer (HSO₄⁻ was the largest peak, together with the dimer (H₂SO₄ · HSO₄⁻ and trimer ((H₂SO₄₂ · HSO₄⁻. SO₅⁻ also tracked HSO₄⁻ at around 20% of the HSO₄⁻ concentration at all times. During the strongest events, the tetramer and a cluster with the tetramer and ammonia were also detected. Quantum chemical calculations predict that sulfuric acid clusters containing ammonia are much more stable when

Model Titan atmospheric hydrocarbon analysis by Ion Mobility Spectrometry in dry helium

International Nuclear Information System (INIS)

Kojiro, D.R.; Stimac, R.M.; Wernlund, R.F.; Cohen, M.J.

1990-01-01

Ion Mobility Spectrometry (IMS) is one analytical technique being investigated for the in situ analysis of the atmosphere of Titan. Any hydrocarbon ions that may form react immediately, in microseconds, with the high concentration of water vapor normally present in conventional IMS. By reducing the water concentration to the parts-per-billion range, the lifetime of the hydrocarbon ions may be increased to the milliseconds required for measurement. At low water level concentrations, other species may become the reactant ion. This study focuses on IMS analysis of expected Titan atmospheric hydrocarbons under very dry, low water concentration conditions

Effect of simultaneous ion irradiation on microstructural change of SiC/SiC composites at high temperature

International Nuclear Information System (INIS)

Taguchi, T.; Wakai, E.; Igawa, N.; Nogami, S.; Snead, L.L.; Hasegawa, A.; Jitsukawa, S.

2002-01-01

The effect of simultaneous triple ion irradiation of He, H and Si on microstructural evolution of two kinds of SiC/SiC composites (HNS composite (using Hi-Nicalon type S SiC fiber) and TSA composite (using Tyranno SA SiC fiber)) at 1000 deg. C has been investigated. The microstructure observations of SiC/SiC composites irradiated to 10 dpa were examined by transmission electron microscopy. He bubbles were hardly formed in matrix of TSA composite, but many helium bubbles and some cracks were observed at grain boundaries of matrix of HNS composite. He bubbles and cracks were not, on the other hand, observed in the both fiber fabrics of HNS and TSA composites. Debonding between fiber and carbon layer following irradiation region was not observed in the both composites. Under these irradiation conditions, TSA composite showed the better microstructural stability against ion beams irradiation than one of HNS composite

Composite ion-exchangers and their possible use in treatment of low/intermediate level liquid radioactive wastes

International Nuclear Information System (INIS)

Sebesta, F.; Motl, A.; John, J.

1993-01-01

A new method of preparation of composite inorganic-organic ion exchangers using modified polyacrylonitrile (PAN) as a binding polymer for the inorganic active component is described. This method enables incorporation of very fine to colloidal particles of active component in the binding polymer which increases the capacity and improves the kinetics of ion exchange of the resulting absorber. The proposed method can be applied on most of the inorganic ion exchangers known. Results of tests of some absorbers for treatment of radioactive wastes produced in the nuclear industry are given. For the removal of radiocesium from Long Term Fuel Storage Pond water at NPP Jaslovske Bohunice (Slovakia) NiFC-PAN composite ion exchanger has been tested. Excellent results have been achieved both at low and high (floating bed) flow rates in the course of treatment of up to 45,000 BV of pond water. The possibility of decreasing the total activity of the Biological Shield water from the same NPP below the 37 Bq/l discharge limit has been proved using NiFC-PAN and NaTiO-PAN composite ion exchangers. NiFC-PAN, NaTiO-PAN, MnO-PAN, M315-PAN and Na-Y-PAN composite ion exchangers were tested for removal of radiocesium, radiocobalt and radiomanganese from standard liquid radioactive wastes and concentrates from NPP Krsko, Croatia. Different combinations of absorbers have been tested for the treatment of Boron Recycle Hold-up, Waste Condensate and Waste Hold-up Tanks. Radium could be quantitatively removed from highly saline acid waste water from uranium underground leaching on Ba(Ca)SO 4 -PAN absorber

Design, fabrication and performance of a mixed-reactant membraneless micro direct methanol fuel cell stack

Science.gov (United States)

Abrego-Martínez, J. C.; Moreno-Zuria, A.; Cuevas-Muñiz, F. M.; Arriaga, L. G.; Sun, Shuhui; Mohamedi, Mohamed

2017-12-01

In the present work, we report the design, fabrication and evaluation of a membraneless mixed-reactant and air-breathing microfluidic direct methanol fuel cell (ML-μDMFC) stack operated in passive mode. The operation under mixed-reactant conditions was achieved by using a highly methanol-tolerant Ag/Pt/CP cathode with ultra-low Pt loading in alkaline medium. Prior to the fabrication of the stack, a flow simulation was made in order to study the behavior of the reactants stream in the microchannel through the 2 cells. Subsequently, the device was tested in passive mode using a mixture of 5 M MeOH +0.5 M KOH. The results showed that by connecting the 2 cells in series, it is possible to effectively double the voltage of a single ML-μDMFC, as well as increasing the absolute power by 75% with practically no cost increase. The stack was capable of operate continuously for more than 2 h with a single charge of 40 μL, producing an OCV of 0.89 V and a maximum power density of 3.33 mW mgPt-1. Additionally, the device exhibited good stability throughout a 10 h test.

Negative ion detachment cross sections: Progress report, March 1, 1985--February 29, 1988

International Nuclear Information System (INIS)

Champion, R.L.; Doverspike, L.D.

1987-08-01

The purpose of the experimental investigations undertaken during the past three years was to perform an extensive and comprehensive study of the collisional dynamics of reactants which involve collisions of negative ions and neutral atomic and molecular targets. The (laboratory) collision energies for these studies ranged from about 1 eV up to 500 eV and the experiments involved measurements of both absolute total cross sections and doubly-differential cross sections. The various processes investigated included electron detachment, charge transfer, dissociative charge transfer and reactive (or rearrangement) scattering. Reactants which were the subject of these investigations included the negative ions O/sup minus/, S/sup minus/, Na/sup minus /, K/sup minus/, Cs/sup minus/, H/sup minus/, D/sup minus/ in collisions with H 2 , D 2 , O 2 , N 2 , CO, CO 2 , CH 4 and the alkali atoms Na, K and Cs

Reactions of PO(x)Cl(y)-ions with O(2)(a1-delta-g), H(2)O, and Cl(2) at 298 K

Science.gov (United States)

2008-03-10

have also been studied to assess the chemistry that would occur if trace amounts of these species reached the flow tube. Most of the POxCly " ions...secondary ion-molecule chemistry [25]. P02~ and PO3" were generated from dimethyl phosphite (Ventron, 99%). The reactant ion of interest was selected

COMPOSITIONS BASED ON PALLADIUM(II AND COPPER(II COMPOUNDS, HALIDE IONS, AND BENTONITE FOR OZONE DECOMPOSITION

Directory of Open Access Journals (Sweden)

T. L. Rakitskaya

2017-05-01

bromide ion. For Cu(II-KBr/N-Bent composition, kinetic and calculation data show that, in the presence of bromide ions, copper(II inhibits the ozone decomposition. For Pd(II-KBr/NBent composition, it has been found that the maximum activity is attained at СPd(II = 1.02·10-5 mol/g. For bimetallic Pd(II- Cu(II-KBr/N-Bent composition, changes in τ0, τ1/2, k1/2, and Q1/2 parameters depending on a Pd(II content are similar to those for monometallic Pd(II-KBr/NBent composition; however, values of the parameters are higher for the monometallic system. Thus, the inhibiting effect of Cu(II is observed even in the presence of palladium(II.

Embedded Si/Graphene Composite Fabricated by Magnesium-Thermal Reduction as Anode Material for Lithium-Ion Batteries

Science.gov (United States)

Zhu, Jiangliu; Ren, Yurong; Yang, Bo; Chen, Wenkai; Ding, Jianning

2017-12-01

Embedded Si/graphene composite was fabricated by a novel method, which was in situ generated SiO2 particles on graphene sheets followed by magnesium-thermal reduction. The tetraethyl orthosilicate (TEOS) and flake graphite was used as original materials. On the one hand, the unique structure of as-obtained composite accommodated the large volume change to some extent. Simultaneously, it enhanced electronic conductivity during Li-ion insertion/extraction. The MR-Si/G composite is used as the anode material for lithium ion batteries, which shows high reversible capacity and ascendant cycling stability reach to 950 mAh·g-1 at a current density of 50 mA·g-1 after 60 cycles. These may be conducive to the further advancement of Si-based composite anode design.

Influence of both ion bombardment and chemical treatment processes on the electrical conductivity of PVC/poly aniline composites

International Nuclear Information System (INIS)

Gad, E.A.M.; Ashour, A.H.; Abdel-Hamid, H.M.; Sayed, W.M.

1999-01-01

In this article the changes in the electrical conductivity of PVC/poly aniline composites, as temperature consecutively increases, have been measured. The measurement were taken with correspondence to a control series of the composites under two processes:A. Composite samples bombarded with Ar + ions with fluence 2.44 x 10 13 beam ions /cm 2 ., sec 4 of 4 ke V beam energy where argon atoms can induce defects in the surface layer take place. Composite samples treated chemically with concentrated H 2 SO 4 as dopant which reacts with nitrogen atom in aniline. The measurements were also, done with the composites as the ratio of poly(aniline) stepped upward

Platinum- and membrane-free swiss-roll mixed-reactant alkaline fuel cell.

Science.gov (United States)

Aziznia, Amin; Oloman, Colin W; Gyenge, Előd L

2013-05-01

Eliminating the expensive and failure-prone proton exchange membrane (PEM) together with the platinum-based anode and cathode catalysts would significantly reduce the high capital and operating costs of low-temperature (<373 K) fuel cells. We recently introduced the Swiss-roll mixed-reactant fuel cell (SR-MRFC) concept for borohydride-oxygen alkaline fuel cells. We now present advances in anode electrocatalysis for borohydride electrooxidation through the development of osmium nanoparticulate catalysts supported on porous monolithic carbon fiber materials (referred to as an osmium 3D anode). The borohydride-oxygen SR-MRFC operates at 323 K and near atmospheric pressure, generating a peak power density of 1880 W m(-2) in a single-cell configuration by using an osmium-based anode (with an osmium loading of 0.32 mg cm(-2)) and a manganese dioxide gas-diffusion cathode. To the best of our knowledge, 1880 W m(-2) is the highest power density ever reported for a mixed-reactant fuel cell operating under similar conditions. Furthermore, the performance matches the highest reported power densities for conventional dual chamber PEM direct borohydride fuel cells. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Mesoporous Tin-Based Oxide Nanospheres/Reduced Graphene Composites as Advanced Anodes for Lithium-Ion Half/Full Cells and Sodium-Ion Batteries.

Science.gov (United States)

He, Yanyan; Li, Aihua; Dong, Caifu; Li, Chuanchuan; Xu, Liqiang

2017-10-04

The large volume variations of tin-based oxides hinder their extensive application in the field of lithium-ion batteries (LIBs). In this study, structure design, hybrid fabrication, and carbon-coating approaches have been simultaneously adopted to address these shortcomings. To this end, uniform mesoporous NiO/SnO 2 @rGO, Ni-Sn oxide@rGO, and SnO 2 @rGO nanosphere composites have been selectively fabricated. Among them, the obtained NiO/SnO 2 @rGO composite exhibited a high capacity of 800 mAh g -1 at 1000 mA g -1 after 400 cycles. The electrochemical mechanism of NiO/SnO 2 as an anode for LIBs has been preliminarily investigated by ex situ XRD pattern analysis. Furthermore, an NiO/SnO 2 @rGO-LiCoO 2 lithium-ion full cell showed a high capacity of 467.8 mAh g -1 at 500 mA g -1 after 100 cycles. Notably, the NiO/SnO 2 @rGO composite also showed good performance when investigated as an anode for sodium-ion batteries (SIBs). It is believed that the unique mesoporous nanospherical framework, synergistic effects between the various components, and uniform rGO wrapping of NiO/SnO 2 shorten the Li + ion diffusion pathways, maintain sufficient contact between the active material and the electrolyte, mitigate volume changes, and finally improve the electrical conductivity of the electrode. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

A Spinel-integrated P2-type Layered Composite: High-rate Cathode for Sodium-ion Batteries

Energy Technology Data Exchange (ETDEWEB)

Zheng, Jianming; Yan, Pengfei; Kan, Wang Hay; Wang, Chong M.; Manthiram, Arumugam

2016-01-14

Sodium-ion batteries (SIB) are being intensively investigated, owing to the natural abundance and low cost of Na resources. However, the SIBs still suffer from poor rate capability due to the large ionic radius of Na+ ion and the significant kinetic barrier to Na+-ion transport. Here, we present an Fd-3m spinel-integrated P2-type layered composite (P2 + Fd-3m) material as a high-rate cathode for SIBs. The P2 + Fd-3m composite material Na0.50Ni1/6Co1/6Mn2/3O2 shows significantly enhanced discharge capacity, energy density, and rate capability as compared to the pure P2-type counterpart. The composite delivers a high capacity of 85 mA h g-1 when discharging at a very high current density of 1500 mA g-1 (10C rate) between 2.0 and 4.5 V, validating it as a promising cathode candidate for high-power SIBs. The superior performance is ascribed to the improved kinetics in the presence of the integrated-spinel phase, which facilitates fast electron transport to coordinate with the timely Na+-ion insertion/extraction. The findings of this work also shed light on the importance of developing lattice doping, surface coating, and electrolyte additives to further improve the structural and interfacial stability of P2-type cathode materials and fully realize their practical applications in sodium-ion batteries.

Non-isothermal electrochemical model for lithium-ion cells with composite cathodes

Science.gov (United States)

Basu, Suman; Patil, Rajkumar S.; Ramachandran, Sanoop; Hariharan, Krishnan S.; Kolake, Subramanya Mayya; Song, Taewon; Oh, Dukjin; Yeo, Taejung; Doo, Seokgwang

2015-06-01

Transition metal oxide cathodes for Li-ion batteries offer high energy density and high voltage. Composites of these materials have shown excellent life expectancy and improved thermal performance. In the present work, a comprehensive non-isothermal electrochemical model for a Lithium ion cell with a composite cathode is developed. The present work builds on lithium concentration-dependent diffusivity and thermal gradient of cathode potential, obtained from experiments. The model validation is performed for a wide range of temperature and discharge rates. Excellent agreement is found for high and room temperature with moderate success at low temperatures, which can be attributed to the low fidelity of material properties at low temperature. Although the cell operation is limited by electronic conductivity of NCA at room temperature, at low temperatures a shift in controlling process is seen, and operation is limited by electrolyte transport. At room temperature, the lithium transport in Cathode appears to be the main source of heat generation with entropic heat as the primary contributor at low discharge rates and ohmic heat at high discharge rates respectively. Improvement in electronic conductivity of the cathode is expected to improve the performance of these composite cathodes and pave way for its wider commercialization.

Mass spectrometric studies of bimolecular reactions in a selected ion flow tube (SIFT)

International Nuclear Information System (INIS)

Shul, R.J.; Upschulte, B.L.; Passarella, R.; Keesee, R.G.; Castleman, A.W.

1985-01-01

The rate coefficients for a number of thermal energy charge transfer reactions have been obtained with a selected ion flow tube (SIFT). The reactions studied involve Ar + and Ar 2 + with a variety of neutral molecules including: O 2 , CS 2 , CO 2 , SO 2 , H 2 S, NH 3 , and SF 6 . Such reactions have been of long-standing interest in the field of gas-phase ion-molecule chemistry from both a practical and fundamental point of view. Consideration of charge transfer reactions as possible sources of chemical lasers and their role in ionospheric and interstellar chemistry account for much of the interest. Fundamentally, the mechanism involved in these reactions has yet to be definitively established. The consumption deposition of energy into internal modes and translational degrees of freedom in such reactions has also been a topic of considerable debate. The apparatus consists of five main components: an ion source, SIFT quadrupole, ion injector, flow tube, and a mass spectrometer detection system. Ions formed in a high pressure source leak into a SIFT quadrupole where they are mass selected. The primary ion of interest is then injected into the flow tube where reactions are studied. Once in the flow tube the ions are carried downstream by an inert buffer gas, either argon, nitrogen, or helium in the present study. Neutral reactant gas is added through a reactant gas inlet (RGI) at an appropriate location downstream in the flow tube, and allowed to react with the injected ions. Ions on the flow tube axis are sampled through a 1 mm orifice where they are mass analyzed by a second quadrupole mass spectrometer and detected with a channeltron electron multiplier

Hard carbon coated nano-Si/graphite composite as a high performance anode for Li-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Jeong, Sookyung; Li, Xiaolin; Zheng, Jianming; Yan, Pengfei; Cao, Ruiguo; Jung, Hee Joon; Wang, Chong M.; Liu, Jun; Zhang, Jiguang

2016-08-27

With the ever increasing demands on Li-ion batteries with higher energy densities, alternative anode with higher reversible capacity is required to replace the conventional graphite anode. Here, we demonstrate a cost-effective hydrothermal-carbonization approach to prepare the hard carbon coated nano-Si/graphite (HC-nSi/G) composite as a high performance anode for Li-ion batteries. In this hierarchical structured composite, the hard carbon coating layer not only provides an efficient pathway for electron transfer, but also alleviates the volume variation of silicon during charge/discharge processes. The HC-nSi/G composite electrode shows excellent electrochemical performances including a high specific capacity of 878.6 mAh g-1 based on the total weight of composite, good rate performance and a decent cycling stability, which is promising for practical applications.

Embedded Si/Graphene Composite Fabricated by Magnesium-Thermal Reduction as Anode Material for Lithium-Ion Batteries.

Science.gov (United States)

Zhu, Jiangliu; Ren, Yurong; Yang, Bo; Chen, Wenkai; Ding, Jianning

2017-12-16

Embedded Si/graphene composite was fabricated by a novel method, which was in situ generated SiO 2 particles on graphene sheets followed by magnesium-thermal reduction. The tetraethyl orthosilicate (TEOS) and flake graphite was used as original materials. On the one hand, the unique structure of as-obtained composite accommodated the large volume change to some extent. Simultaneously, it enhanced electronic conductivity during Li-ion insertion/extraction. The MR-Si/G composite is used as the anode material for lithium ion batteries, which shows high reversible capacity and ascendant cycling stability reach to 950 mAh·g -1 at a current density of 50 mA·g -1 after 60 cycles. These may be conducive to the further advancement of Si-based composite anode design.

The general theory of multistage geminate reactions of isolated pairs of reactants. III. Two-stage reversible dissociation in geminate reaction A + A↔C↔B + B

Energy Technology Data Exchange (ETDEWEB)

Kipriyanov, Alexey A.; Kipriyanov, Alexander A.; Doktorov, Alexander B. [Voevodsky Institute of Chemical Kinetics and Combustion, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia and Novosibirsk State University, Novosibirsk 630090 (Russian Federation)

2016-04-14

Specific two-stage reversible reaction A + A↔C↔B + B of the decay of species C reactants by two independent transition channels is considered on the basis of the general theory of multistage reactions of isolated pairs of reactants. It is assumed that at the initial instant of time, the reacting system contains only reactants C. The employed general approach has made it possible to consider, in the general case, the inhomogeneous initial distribution of reactants, and avoid application of model concepts of a reaction system structure (i.e., of the structure of reactants and their molecular mobility). Slowing of multistage reaction kinetics as compared to the kinetics of elementary stages is established and physically interpreted. To test approximations (point approximation) used to develop a universal kinetic law, a widely employed specific model of spherical particles with isotropic reactivity diffusing in solution is applied. With this particular model as an example, ultimate kinetics of chemical conversion of reactants is investigated. The question concerning the depths of chemical transformation at which long-term asymptotes are reached is studied.

Chemical vapor composites (CVC)

International Nuclear Information System (INIS)

Reagan, P.

1993-01-01

The Chemical Vapor Composite, CVC trademark , process fabricates composite material by simply mixing particles (powders and or fibers) with CVD reactants which are transported and co-deposited on a hot substrate. A key feature of the CVC process is the control provided by varing the density, geometry (aspect ratio) and composition of the entrained particles in the matrix material, during deposition. The process can fabricate composite components to net shape (± 0.013 mm) on a machined substrate in a single step. The microstructure of the deposit is described and several examples of different types of particles in the matrix are illustrated. Mechanical properties of SiC composite material fabricated with SiC powder and fiber will be presented. Several examples of low cost ceramic composite products will be shown. (orig.)

Composition of atmospheric precipitation. I. Sampling technique. Use of ion exchange resins

Energy Technology Data Exchange (ETDEWEB)

Egner, H; Eriksson, E; Emanuelsson, A

1947-01-01

In order to investigate the composition of atmospheric precipitations in Sweden, a technique using ion exchange resins has been developed. The possibilities of nitrate reduction, and ammonia losses, when the precipitation is collected in zinc gauges is stressed. Glass funnels are used, and they are effectively protected from bird droppings. The ion exchange resins so far available are quite serviceable but show some deficiencies as to stability, and activity in alkaline solutions. New resins, which are not yet available, seem to offer definite advantages.

Media ion composition controls regulatory and virulence response of Salmonella in spaceflight.

Directory of Open Access Journals (Sweden)

James W Wilson

Full Text Available The spaceflight environment is relevant to conditions encountered by pathogens during the course of infection and induces novel changes in microbial pathogenesis not observed using conventional methods. It is unclear how microbial cells sense spaceflight-associated changes to their growth environment and orchestrate corresponding changes in molecular and physiological phenotypes relevant to the infection process. Here we report that spaceflight-induced increases in Salmonella virulence are regulated by media ion composition, and that phosphate ion is sufficient to alter related pathogenesis responses in a spaceflight analogue model. Using whole genome microarray and proteomic analyses from two independent Space Shuttle missions, we identified evolutionarily conserved molecular pathways in Salmonella that respond to spaceflight under all media compositions tested. Identification of conserved regulatory paradigms opens new avenues to control microbial responses during the infection process and holds promise to provide an improved understanding of human health and disease on Earth.

Cassini CAPS Identification of Pickup Ion Compositions at Rhea

Science.gov (United States)

Desai, R. T.; Taylor, S. A.; Regoli, L. H.; Coates, A. J.; Nordheim, T. A.; Cordiner, M. A.; Teolis, B. D.; Thomsen, M. F.; Johnson, R. E.; Jones, G. H.; Cowee, M. M.; Waite, J. H.

2018-02-01

Saturn's largest icy moon, Rhea, hosts a tenuous surface-sputtered exosphere composed primarily of molecular oxygen and carbon dioxide. In this Letter, we examine Cassini Plasma Spectrometer velocity space distributions near Rhea and confirm that Cassini detected nongyrotropic fluxes of outflowing CO2+ during both the R1 and R1.5 encounters. Accounting for this nongyrotropy, we show that these possess comparable along-track densities of ˜2 × 10-3 cm-3. Negatively charged pickup ions, also detected during R1, are surprisingly shown as consistent with mass 26 ± 3 u which we suggest are carbon-based compounds, such as CN-, C2H-, C2-, or HCO-, sputtered from carbonaceous material on the moon's surface. The negative ions are calculated to possess along-track densities of ˜5 × 10-4 cm-3 and are suggested to derive from exogenic compounds, a finding consistent with the existence of Rhea's dynamic CO2 exosphere and surprisingly low O2 sputtering yields. These pickup ions provide important context for understanding the exospheric and surface ice composition of Rhea and of other icy moons which exhibit similar characteristics.

Adsorption Effectivity Test of Andisols Clay-Zeolite (ACZ) Composite as Chromium Hexavalent (Cr(VI)) Ion Adsorbent

Science.gov (United States)

Pranoto; Masykur, A.; Nugroho, Y. A.

2018-03-01

Adsorption of chromium hexavalent (Cr(VI)) ion in aqueous solution was investigated. This research was purposed to study the influence of the composition of ACZ, temperature activation, and contact time against adsorption capacity of Cr(VI) ion in aqueous solution. Determination of adsorption effectivity using several parameter such as composition variation of ACZ, contact time, pH, activation temperature, and concentration. In this research, andisol clay and zeolite has been activated with NaOH 3 M and 1 M, respectively. Temperature variation used 100, 200, and 400°C. While composition variation ACZ used 0:100, 25:75, 50:50, 75:25, 100:0. The pH variation was used 2 – 6 and concentration variation using 2, 4, 6, 8, 10, and 12 ppm. Characterization in this research used such as UV-Vis, Surface Area Analyzer (SAA) and Acidity Analysis. Result of this research is known that optimum composition of ACZ was 50:50 with calcination temperature 100°C. Optimum adsorption of Cr(VI) at pH 4 with removal percentage 76.10 % with initial concentration 2 ppm and adsorption capacity is 0.16 mg/g. Adsorption isotherm following freundlich isotherm with value Kf = 0.17 mg/g and value n is 0.963. Based on results, ACZ composite can be used as Cr(VI) ion adsorbents in aqueous solutions.

Dependence of secondary ion emission current on the composition of beryllium-nickel alloys

International Nuclear Information System (INIS)

Pistryak, V.M.; Kozlov, V.F.; Tikhinskij, G.F.; Fogel', Ya.M.

1976-01-01

The dependence is studied of the secondary ions emission current on the composition of beryllium-nickel alloys. It is established that appearance of intermetallide phases in the Be-Ni alloys has no effect on the linear character of the secondary ions Ni + and Be + of emission current. The phase transformation from the solid solution to the compound Ni 5 Be 21 with a change in the alloys concentration is fixed by appearance of the secondary ion NiBe + emission. The limited solubility of nickel in solid beryllium at a temperature close to room temperature is determined to be equal to 1.3+-0.27 at%

Ion release from a composite resin after exposure to different 10% carbamide peroxide bleaching agents

Directory of Open Access Journals (Sweden)

Renata Plá Rizzolo Bueno

2012-06-01

Full Text Available OBJECTIVE: This in vitro study evaluated the influence of two 10% carbamide peroxide bleaching agents - a commercial product (Opalescence PF; Ultradent Products, Inc. and a bleaching agent prepared in a compounding pharmacy - on the chemical degradation of a light-activated composite resin by determining its release of ions before and after exposure to the agents. MATERIAL AND METHODS: Thirty composite resin (Filtek Z250; 3M/ESPE samples were divided into three groups: group I (exposed to Opalescence PF commercial bleaching agent, group II (exposed to a compounded bleaching agent and group III (control - Milli-Q water. After 14 days of exposure, with a protocol of 8 h of daily exposure to the bleaching agents and 16 h of immersion in Milli-Q water, the analysis of ion release was carried out using a HP 8453 spectrophotometer. The values were analyzed statistically by ANOVA, Tukey's test and the paired t-tests. The significance level was set at 5%. RESULTS: After 14 days of the experiment, statistically significant difference was found between group II and groups I and III, with greater ion release from the composite resin in group II. CONCLUSIONS: The compounded bleaching agent had a more aggressive effect on the composite resin after 14 days of exposure than the commercial product and the control (no bleaching.

Interweaved Si@C/CNTs and CNFs composites as anode materials for Li-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Zhang, Miao [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Hou, Xianhua, E-mail: houxh@scnu.edu.cn [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Engineering Research Center of Materials and Technology for Electrochemical Energy Storage Ministry of Education, Guangzhou 510006 (China); Wang, Jie; Li, Min [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Hu, Shejun [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Engineering Research Center of Materials and Technology for Electrochemical Energy Storage Ministry of Education, Guangzhou 510006 (China); Shao, Zongping [Nanjing University of Technology, College of Chemistry and Chemical Engineering, Nanjing 210009 (China); Liu, Xiang [Institute of Advanced Materials, Nanjing University of Technology, Nanjing 210009 (China)

2014-03-05

Graphical abstract: In summary, a serious of high-energy wet ball milling, closed spray drying and subsequent chemical vapor deposition methods were introduced successfully to fabricated novel Si@C/CNTs and CNFs composites with carbon nanotubes and carbon nanofibres interweaved with carbon coated silicon spherical composites as superior anodes in lithium-ion batteries. The core-shell structure of Si@C composites can accommodate the volume change of electrode during charge and discharge. Meanwhile, the citric acid pyrolyzed carbon was coated on the surface of the silicon perfectly and constructs the connection network of nano silicon particles. Moreover, the carbon nanotubes and carbon nanofibres, which is interweaved with nano-silicon, also allows high electrical conductivity, improved solid–electrolyte interface formation and structural integrity. Compared with pure silicon and Si@C composites, the novel Si@C/CNTs and CNFs composites had the best combination of reversible capacity and cycleablity, and this anode materials exhibited excellent electrochemical performance. The Si/C composite had a fairly high initial discharge capacity of 2168.7 mA h g{sup −1} with an efficiency of 73%, and the discharge capacity of the 50th cycle maintained surprisingly of 1194.9 mA h g{sup −1}. Meanwhile, spray drying and chemical vapor deposition are environmentally friendly, economical, and relatively high-yield method for the production of the Si@C/CNTs and CNFs composites in large quantities. Consequently, the novel Si@C/CNTs and CNFs composite electrodes may be a potential alternative to graphite for high energy density lithium ion batteries. Highlights: • The core/shell structured silicon/carbon composites were prepared by a facile way. • The as-prepared Si@C/CNTs and CNFs composites shows excellent electrochemical performance. • The preparation method has mild experiment conditions and high production rate. • The structure benefited electronic transfer and

Vibrational-state-selected ion--molecule reaction cross sections at thermal energies

NARCIS (Netherlands)

Pijkeren, D. van; Boltjes, E.; Eck, J. van; Niehaus, A.

1984-01-01

A method designed to measure relative ion—molecule reaction rates at thermal collision energies for selected reactant ion vibrational states is described. Relative reaction rates are determined for the three endothermic reactions: H2+ (υ)(He,H)HeH+, H2+ (υ)(Ne,H)NeH+, D2+(υ)(Ne, D)NeD+, and for the

Copper nanofiber-networked cobalt oxide composites for high performance Li-ion batteries

Directory of Open Access Journals (Sweden)

Shim Hee-Sang

2011-01-01

Full Text Available Abstract We prepared a composite electrode structure consisting of copper nanofiber-networked cobalt oxide (CuNFs@CoO x . The copper nanofibers (CuNFs were fabricated on a substrate with formation of a network structure, which may have potential for improving electron percolation and retarding film deformation during the discharging/charging process over the electroactive cobalt oxide. Compared to bare CoO x thin-film (CoO x TF electrodes, the CuNFs@CoO x electrodes exhibited a significant enhancement of rate performance by at least six-fold at an input current density of 3C-rate. Such enhanced Li-ion storage performance may be associated with modified electrode structure at the nanoscale, improved charge transfer, and facile stress relaxation from the embedded CuNF network. Consequently, the CuNFs@CoO x composite structure demonstrated here can be used as a promising high-performance electrode for Li-ion batteries.

Preparation of Nafion 117™-SnO₂ Composite Membranes using an Ion-Exchange Method

DEFF Research Database (Denmark)

Nørgaard, Casper Frydendal; Nielsen, Ulla Gro; Skou, Eivind Morten

2012-01-01

Nafion 117™-SnO2 composite membranes were prepared by in-situ particle formation using an ion-exchange method. SnO2 was incorporated into Nafion 117ä membranes by ion-exchange in solutions of SnCl2 ∙2 H2O in methanol, followed by oxidation to SnO2 in air. By adjustment of the concentration of SnCl2...... ∙ 2 H2O used in the ion-exchange step, compositions ranging from 2 to 8 wt% SnO2 with SnO2 homogeneously distributed as nanoparticles were obtained. The prepared nanocomposite membranes were characterized by powder XRD, 119Sn MAS NMR spectroscopy, electrochemical impedance spectroscopy, water uptake...

Automation of a battery of ion exchange columns for the determination of Pu in biological samples

International Nuclear Information System (INIS)

Jeanmaire, L.; Ballada, J.; Rigaudiere, R.; Patti, F.; Clanet, F.

1967-01-01

The document describes an apparatus allowing ten automatic and simultaneous determination of plutonium by ion exchange resins in urine. The constant flow rate reactants supply is realized by plastic siphons. The different determination phases are controlled by a programmer. (A.L.B.) [fr

Electrodeposited Germanium/Carbon Composite as an Anode Material for Lithium Ion Batteries

International Nuclear Information System (INIS)

Kim, Sang-Wan; Ngo, Duc Tung; Heo, Jaeyeong; Park, Choong-Nyeon; Park, Chan-Jin

2017-01-01

Highlights: • Electrodeposition was applied for the synthesis of Ge/C composite. • High coulombic efficiency of ∼85% in the first cycle was attained for Ge/C composite. • Full cell of Ge/C-LiCoO 2 exhibits excellent electrochemical performance, without pre-lithiation of Ge/C. - Abstract: We demonstrate the synthesis of nano Ge/C composite using a facile and cost-effective electrochemical deposition method, and its application as an anode material in Li-ion batteries. Nano Ge/C composite is electrodeposited directly on Cu foil in ethylene glycol containing GeCl 4 and carbon black. The Ge particles with an average size of ∼20 nm are uniformly covered with carbon. Compared with the pure Ge electrode, the Ge/C electrode exhibits a higher first reversible capacity of 1224 mA g −1 , and maintains a capacity of 1095 mAh g −1 at 0.1C over 50 cycles. Even at the high rate of 2C, the capacity of the Ge/C electrode is still high at 972 mAh g −1 . The presence of carbon black and pores in the Ge/C electrode improves the conductivity of the electrode, and mitigates the stress inside the electrode by supplying buffer volume, leading to the enhanced electrochemical characteristics of the electrode. Further, the full Li-ion cell composed of Ge/C anode and LiCoO 2 cathode exhibits good cyclability, rate capability, and coulombic efficiency.

Nanostructured Si/TiC composite anode for Li-ion batteries

International Nuclear Information System (INIS)

Zeng, Z.Y.; Tu, J.P.; Yang, Y.Z.; Xiang, J.Y.; Huang, X.H.; Mao, F.; Ma, M.

2008-01-01

Si/TiC nanocomposite anode was synthesized by a surface sol-gel method in combination with a following heat-treatment process. Through this process, nanosized Si was homogeneously distributed in a titanium carbide matrix. The electrochemically less active TiC working as a buffer matrix successfully prevented Si from cracking/crumbling during the charging/discharging process. The interspaces in the Si/TiC nanocomposite could offer convenient channels for Li ions to react with active Si. The Si/TiC composite exhibited a reversible charge/discharge capacity of about 1000 mAh g -1 with average discharge capacity fading of 1.8 mAh g -1 (0.18%) from 2nd to 100th cycle, indicating its excellent cyclability when used as anode materials for lithium-ion batteries

Serum levels of chicken mannan-binding lectin (MBL) during virus infections; indication that chicken MBL is an acute phase reactant

DEFF Research Database (Denmark)

Nielsen, O.L.; Jensenius, J. C.; Jørgensen, Poul Henrik

1999-01-01

Mannan-binding lectin (MBL) is a serum collectin which is believed to be an opsonin of the innate immune defence against various microorganisms. MBL is a minor acute phase reactant in man. We investigated the concentration of serum MBL in chickens infected with infectious bronchitis virus (IBV...... levels returned to normal values 6-10 days after infection. The results indicated that MBL is a minor acute phase reactant in chickens....

Biomass carbon composited FeS2 as cathode materials for high-rate rechargeable lithium-ion battery

Science.gov (United States)

Xu, Xin; Meng, Zhen; Zhu, Xueling; Zhang, Shunlong; Han, Wei-Qiang

2018-03-01

Pyrite FeS2 has long been used as commercial primary lithium batteries at room temperature. To achieve rechargeable FeS2 battery, biomass-carbon@FeS2 composites are prepared using green and renewable auricularia auricula as carbon source through the process of carbonization and sulfuration. The auricularia auricula has strong swelling characteristics to absorb aqueous solution which can effectively absorb Fe ions into its body. FeS2 homogeneously distributed in biomass carbon matrix performs high electronic and ionic conductivity. The specific capacity of biomass-carbon@FeS2 composites remains 850 mAh g-1 after 80 cycles at 0.5C and 700 mAh g-1 at the rate of 2C after 150 cycles. Biomass-carbon@FeS2 composites exhibit high-rate capacity in lithium-ion battery.

The general theory of multistage geminate reactions of isolated pairs of reactants. III. Two-stage reversible dissociation in geminate reaction A + A ↔ C ↔ B + B.

Science.gov (United States)

Kipriyanov, Alexey A; Kipriyanov, Alexander A; Doktorov, Alexander B

2016-04-14

Specific two-stage reversible reaction A + A ↔ C ↔ B + B of the decay of species C reactants by two independent transition channels is considered on the basis of the general theory of multistage reactions of isolated pairs of reactants. It is assumed that at the initial instant of time, the reacting system contains only reactants C. The employed general approach has made it possible to consider, in the general case, the inhomogeneous initial distribution of reactants, and avoid application of model concepts of a reaction system structure (i.e., of the structure of reactants and their molecular mobility). Slowing of multistage reaction kinetics as compared to the kinetics of elementary stages is established and physically interpreted. To test approximations (point approximation) used to develop a universal kinetic law, a widely employed specific model of spherical particles with isotropic reactivity diffusing in solution is applied. With this particular model as an example, ultimate kinetics of chemical conversion of reactants is investigated. The question concerning the depths of chemical transformation at which long-term asymptotes are reached is studied.

Metal Palladium Dispersed Inside Macroporous Ion-Exchange Resins: Textural Characterization and Accessibility to Gaseou Reactants

Czech Academy of Sciences Publication Activity Database

Biffis, A.; Jeřábek, Karel; D'Archivio, A. A.; Galantini, L.; Corain, B.

2000-01-01

Roč. 130, - (2000), s. 2327-2332 ISSN 0167-2991. [International Congress on Catalysis /12./. Granada, 09.07.2000-14.07.2000] Institutional research plan: CEZ:AV0Z4072921 Keywords : metal palladium * dispersed * ion-exchange resins Subject RIV: CI - Industrial Chemistry, Chemical Engineering Impact factor: 0.513, year: 2000

Mechanical characterization and ion release of bioactive dental composites containing calcium phosphate particles.

Science.gov (United States)

Natale, Livia C; Rodrigues, Marcela C; Alania, Yvette; Chiari, Marina D S; Boaro, Leticia C C; Cotrim, Marycel; Vega, Oscar; Braga, Roberto R

2018-08-01

to verify the effect of the addition of dicalcium phosphate dihydrate (DCPD) particles functionalized with di- or triethylene glycol dimethacrylate (DEGDMA or TEGDMA) on the degree of conversion (DC), post-gel shrinkage (PS), mechanical properties, and ion release of experimental composites. Four composites were prepared containing a BisGMA/TEGDMA matrix and 60 vol% of fillers. The positive control contained only barium glass fillers, while in the other composites 15 vol% of the barium was replaced by DCPD. Besides the functionalized particles, non-functionalized DCPD was also tested. DC after 24 h (n = 3) was determined by FTIR spectroscopy. The strain gage method was used to obtain PS 5 min after photoactivation (n = 5). Flexural strength and modulus (n = 10) were calculated based on the biaxial flexural test results, after specimen storage for 24 h or 60 days in water. The same storage times were used for fracture toughness testing (FT, n = 10). Calcium and phosphate release up to 60 days was quantified by ICP-OES (n = 3). Data were analyzed by ANOVA/Tukey test (alpha: 5%). Composites containing functionalized DCPD presented higher DC than the control (p composites (p composite with DEGDMA-functionalized DCPD presented fracture strength similar to the control, while for flexural modulus only the composite with TEGDMA-functionalized particles was lower than the control (p composites containing DCPD was higher than the control after 60 days (p composite with non-functionalized DCPD at 15 days and no significant reductions were observed for composites with functionalized DCPD during the observation period (p composites, phosphate release was higher at 15 days than in the subsequent periods, and no difference among them was recorded at 45 and 60 days (p composite with DEGDMA-functionalized particles was the only material with strength similar to the control after 60 days in water; however, it also presented the highest

Compositional changes of human hair melanin resulting from bleach treatment investigated by nanoscale secondary ion mass spectrometry.

Science.gov (United States)

Kojima, Toru; Yamada, Hiromi; Isobe, Mitsuru; Yamamoto, Toshihiko; Takeuchi, Miyuki; Aoki, Dan; Matsushita, Yasuyuki; Fukushima, Kazuhiko

2014-11-01

It is important to understand the influence of bleach treatment on human hair because it is one of the most important chemical treatments in hair cosmetic processes. A comparison of the elemental composition of melanin between virgin hair and bleached hair would provide important information about the structural changes of melanin. To investigate the elemental composition of melanin granules in virgin black hair and bleached hair, these hair cross-sections are analyzed by using a nanoscale secondary ion mass spectrometry (NanoSIMS). The virgin black hair and bleached hair samples were embedded in resin and smooth hair cross-sections were obtained using an ultramicrotome. NanoSIMS measurements were performed using a Cs(+) primary ion beam to detect negative secondary ions. More intensive (16) O(-) ions were detected from the melanin granules of bleached hair than from those of virgin black hair in NanoSIMS (16) O(-) ion image. In addition, it was indicated that (16) O(-) ion intensity and (16) O(-) /(12) C(14) N(-) ion intensity ratio of melanin granules in bleached hair were higher than those in virgin black hair. Nanoscale secondary ion mass spectrometry analysis of the cross-sections of virgin black hair and bleached hair indicated that the oxygen content in melanin granules was increased by bleach treatment. © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Solar Ion Processing of Major Element Surface Compositions of Mature Mare Soils: Insights from Combined XPS and Analytical TEM Observations

Science.gov (United States)

Christoffersen, R.; Dukes, C.; Keller, L. P.; Baragiola, R.

2012-01-01

Solar wind ions are capable of altering the sur-face chemistry of the lunar regolith by a number of mechanisms including preferential sputtering, radiation-enhanced diffusion and sputter erosion of space weathered surfaces containing pre-existing compositional profiles. We have previously reported in-situ ion irradiation experiments supported by X-ray photoelectron spectroscopy (XPS) and analytical TEM that show how solar ions potentially drive Fe and Ti reduction at the monolayer scale as well as the 10-100 nm depth scale in lunar soils [1]. Here we report experimental data on the effect of ion irradiation on the major element surface composition in a mature mare soil.

Self-standing paper based anodes prepared from siliconcarbonitride-MoS2 composite for Li-ion battery applications

Science.gov (United States)

David, Lamuel; Singh, Gurpreet

2013-03-01

We study synthesis of free-standing polymer derived SiCN/ MoS2 composite paper anode for Li-ion battery application. This was achieved following a two-step approach: First, polysilazane was interfaced with exfoliated MoS2 nanosheets which upon pyrolysis resulted in SiCN/MoS2 composite. Second, dispersion of SiCN/MoS2 in isopropanol was vacuum filtered resulting in formation of a self-standing composite paper. Physical and chemical characterization of the composite was carried out by use of electron microscopy, Fourier transform infrared spectroscopy (FT-IR) and Thermo-gravimetric analysis (TGA). FT-IR data indicated complete conversion of polysilazane precursor to SiCN ceramic, while electron microscopy confirmed layered structure of the paper. Thermo-gravimetric analysis showed enhanced thermodynamic stability of the composite paper up to 800 °C. Electrochemical analysis of SiCN/MoS2 composite paper anodes showed that Li-ion can reversible intercalate in the voltage range of 0-2.5 V with a first cycle discharge capacity of 770 mAh/g at a current density of 100 mA/g.

Use of Composite Sorbents for the Removal of Copper (II ions from Aqueous Solution

Directory of Open Access Journals (Sweden)

Rebecca Oyedoyin Adeeyo

2015-01-01

Full Text Available Composite adsorbents are synthesized from two or more materials with different chemical and physical properties in order to increase their selectivity and the reusability. Researchers have developed and applied several novel composite materials for enhancing the removal of heavy metal. In this review, extensive list of composites developed via advanced technologies with specified characteristics for the removal of Cu (II ion are discussed. Emphases on their adsorption capacities, reusability, desorption and regeneration with improved mechanical strengths are presented. Conclusively, prospects and other challenges to be checked and addressed in future are outlined.

Removal of Cr(VI and Toxic Ions from Aqueous Solutions and Tannery Wastewater Using Polymer-Clay Composites

Directory of Open Access Journals (Sweden)

Abd El-Azeem Sallam

2017-10-01

Full Text Available Polymer-clay composites were prepared by natural zeolite (clinoptilolite or naturally local clay deposits in an N,N-methylene-bis-acrylamide as cross-linked. The resultant composites were used for the removal of Cr(VI from an aqueous solution. Additionally, their effects on soluble ions of tannery wastewater were investigated. The produced composites were characterized using X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FT-IR, and scanning electron microscopy (SEM. The results showed that Cr(VI removal is dependent upon initial concentrations and pH. The adsorption quantity of Cr(VI onto the polymerized clay deposit followed by polymerized zeolite exhibited higher values than their original samples. The polymer-clay composite of clay deposit showed the highest removal of 76.3–100% overall initial concentrations of 10–50 mg L−1 and at initial pH of 2. Kinetics of Cr(VI removal by various sorbents was predicted using a pseudo–second order model. Our findings showed that the levels of salinity and various soluble ions (Cr2+, Na+, Cl− and SO42− in tannery wastewater are very high, and their levels were reduced after treatment, especially by polymerized sorbents. It could be concluded that the polymer-clay composites may be employed as a highly efficient sorbent for the removal of Cr(VI and toxic ions from the wastewater.

Structure-phase composition and nano hardness of chrome-fullerite-chrome films irradiated by boron ions

International Nuclear Information System (INIS)

Baran, L.V.

2015-01-01

By methods of atomic force microscopy, X-ray diffraction and nano indentation the research of change of structure phase composition and nano hardness of the chrome - fullerite - chrome films, subjected to implantation by B + ions (E = 80 keV, F = 5*10 17 ions/cm 2 ) are submitted. It is established, that as a result of Boron ion implantation of the chrome - fullerite - chrome films, chrome and fullerite inter fusion on sues, that is the solid-phase interaction and as a result of which forms the heterophase with increased nano hardness. (authors)

Fabrication and modification of metal nanocluster composites using ion and laser beams

International Nuclear Information System (INIS)

Haglund, R.F. Jr.; Osborne, D.H. Jr.; Magruder, R.H. III; White, C.W.; Zuhr, R.A.; Townsend, P.D.; Hole, D.E.; Leuchtner, R.E.

1994-12-01

Metal nanocluster composites have attractive properties for applications in nonlinear optics. However, traditional fabrication techniques -- using melt-glass substrates -- are severely constrained by equilibrium thermodynamics and kinetics. This paper describes the fabrication of metal nanoclusters in both crystalline and glassy hosts by ion implantation and pulsed laser deposition. The size and size distribution of the metal nanoclusters can be modified by controlling substrate temperature during implantation, by subsequent thermal annealing, or by laser irradiation. The authors have characterized the optical response of the composites by absorption and third-order nonlinear-optical spectroscopies; electron and scanning-probe microscopies have been used to benchmark the physical characteristics of the composites. The outlook for controlling the structure and nonlinear optical response properties of these nanophase materials appears increasingly promising

Electrogenerated chemiluminescence of tris(2,2' bipyridine)ruthenium(II) using common biological buffers as co-reactant, pH buffer and supporting electrolyte.

Science.gov (United States)

Kebede, Noah; Francis, Paul S; Barbante, Gregory J; Hogan, Conor F

2015-11-07

A series of aliphatic tertiary amines (HEPES, POPSO, EPPS and BIS-TRIS) commonly used to buffer the pH in biological experiments, were examined as alternative, non-toxic co-reactants for the electrogenerated chemiluminescence (ECL) of tris(2,2'-bipyridine)ruthenium(ii) ([Ru(bpy)3](2+)). These were found to be very attractive as "multi-tasking" reagents, serving not only as co-reactants, but also fulfiling the roles of pH buffer and supporting electrolyte within an aqueous environment; thus significantly simplifying the overall ECL analysis. Sub-nanomolar detection limits were obtained for [Ru(bpy)3](2+) in the presence of BIS-TRIS, making this species an valuable option for co-reactant ECL-based bioanalytical applications.

Stable silicon/3D porous N-doped graphene composite for lithium-ion battery anodes with self-assembly

Science.gov (United States)

Tang, Xiaofu; Wen, Guangwu; Song, Yan

2018-04-01

We fabricate a novel 3D N-doped graphene/silicon composite for lithium-ion battery anodes, with Si nanoparticles uniformly dispersed and thoroughly embedded in the N-doped graphene matrix. The favorable structure of the composite results in a BET surface area and an average mesopore diameter of 189.2 m2 g-1 and 3.82 nm, respectively. The composite delivers reversible capacities as high as 1132 mA h g-1 after 100 cycles under a current of 5 A g-1 and 1017 mA h g-1 after 200 cycles at 1 A g-1, and exhibits an improved rate capability. The present approach shows promise for the preparation of other high-performance anode materials for lithium-ion batteries.

Synthesis and characterization of polyacrylamide zirconium (IV iodate ion-exchanger: Its application for selective removal of lead (II from wastewater

Directory of Open Access Journals (Sweden)

Nafisur Rahman

2017-05-01

Full Text Available Polyacrylamide zirconium (IV iodate was synthesized using the sol–gel technique. The synthesis conditions such as reactant concentrations and temperature were changed to optimize the ion exchange properties of the hybrid organic–inorganic ion exchange material. Zirconium oxychloride (0.1 M was added to 0.1 M potassium iodate in the presence of 0.4 M acrylamide and heated at 70 °C for 6 h to yield the polyacrylamide zirconium (IV iodate with maximum capacity. The ion exchange capacity was found to be 3.27 meq/g for Pb(II. The hybrid material has been characterized on the basis of chemical composition FTIR, XRD, TGA-DTA, SEM and EDX studies. Sorption studies showed that the hybrid cation exchanger has a high selectivity to Pb(II in comparison to other metal ions. Its selectivity was evaluated by performing some important binary separations like Hg(II–Pb(II, Cu(II–Pb(II, Ni(II–Pb(II, Fe(III–Pb(II and Cd(II–Pb(II. In addition, the selective separation of Pb(II was also achieved from a synthetic mixture containing a large number of metal ions with a recovery of ∼98.5%. The proposed method was successfully applied for the selective removal of Pb(II from wastewater samples.

Mobility and molecular ions of dimethyl methyl phosphonate, methyl salicylate and acetone

Science.gov (United States)

Nowak, D. M.

1983-06-01

The mobilities of positive and negative reactant ions are reported for (H2O)nH(+); (H2O)2O2 and (H2O)2CO3(-) ion clusters. The formation of positive DMMP monomer and dimer is reported, and equilbria molecular reactions are reported. Acetone is reported as forming a dimer at 81 ppb with a reduced mobility (K sub o) of 1.82, Methyl salicylate is shown to form a protonated and hydrated positive monomer. Mixtures of DMMP and methyl salicylate with acetone showed a substantial change in DMMP ion clustering and little or no change in the methyl salicylate mobility spectra. Negative ions were not observed for DMMP, methyl salicylate, acetone and the mixtures under the conditions reported.

Real-time detection of metal ions using conjugated polymer composite papers.

Science.gov (United States)

Lee, Ji Eun; Shim, Hyeon Woo; Kwon, Oh Seok; Huh, Yang-Il; Yoon, Hyeonseok

2014-09-21

Cellulose, a natural polymeric material, has widespread technical applications because of its inherent structural rigidity and high surface area. As a conjugated polymer, polypyrrole shows practical potential for a diverse and promising range of future technologies. Here, we demonstrate a strategy for the real-time detection and removal of metal ions with polypyrrole/cellulose (PPCL) composite papers in solution. Simply, the conjugated polymer papers had different chemical/physical properties by applying different potentials to them, which resulted in differentiable response patterns and adsorption efficiencies for individual metal ions. First, large-area PPCL papers with a diameter of 5 cm were readily obtained via vapor deposition polymerization. The papers exhibited both mechanical flexibility and robustness, in which polypyrrole retained its redox property perfectly. The ability of the PPCL papers to recognize metal ions was examined in static and flow cells, in which real-time current change was monitored at five different applied potentials (+1, +0.5, 0, -0.5, and -1 V vs. Ag/AgCl). Distinguishable signals in the PPCL paper responses were observed for individual metal ions through principal component analysis. Particularly, the PPCL papers yielded unique signatures for three metal ions, Hg(ii), Ag(i), and Cr(iii), even in a real sample, groundwater. The sorption of metal ions by PPCL papers was examined in the flow system. The PPCL papers had a greatly superior adsorption efficiency for Hg(ii) compared to that of the other metal ions. With the strong demand for the development of inexpensive, flexible, light-weight, and environmentally friendly devices, the fascinating characteristics of these PPCL papers are likely to provide good opportunities for low-cost paper-based flexible or wearable devices.

An Amorphous Carbon Nitride Composite Derived from ZIF-8 as Anode Material for Sodium-Ion Batteries.

Science.gov (United States)

Fan, Jing-Min; Chen, Jia-Jia; Zhang, Qian; Chen, Bin-Bin; Zang, Jun; Zheng, Ming-Sen; Dong, Quan-Feng

2015-06-08

An composite comprising amorphous carbon nitride (ACN) and zinc oxide is derived from ZIF-8 by pyrolysis. The composite is a promising anode material for sodium-ion batteries. The nitrogen content of the ACN composite is as high as 20.4 %, and the bonding state of nitrogen is mostly pyridinic, as determined by X-ray photoelectron spectroscopy (XPS). The composite exhibits an excellent Na(+) storage performance with a reversible capacity of 430 mA h g(-1) and 146 mA h g(-1) at current densities of 83 mA g(-1) and 8.33 A g(-1) , respectively. A specific capacity of 175 mA h g(-1) was maintained after 2000 cycles at 1.67 A g(-1) , with only 0.016 % capacity degradation per cycle. Moreover, an accelerating rate calorimetry (ARC) test demonstrates the excellent thermal stability of the composite, with a low self heating rate and high onset temperature (210 °C). These results shows its promise as a candidate material for high-capacity, high-rate anodes for sodium-ion batteries. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Electron capture by multicharged ions at eV energies

International Nuclear Information System (INIS)

Havener, C.C.; Huq, M.S.; Meyer, F.W.; Phaneuf, R.A.

1988-01-01

A multicharged ion-atom merged-beams apparatus has been used in conjunction with the ORNL-ECR ion source to measure accurate absolute electron-capture cross sections in the energy range from below 1 eV/amu to 1500 eV/amu. Measurements for N/sup 3+,4+,5+/ /plus/ H(D) collisions indicate good agreement with available theoretical calculations. However, measurements with O 5+ /plus/ H(D) show an unexpected low-energy behavior which may be attributable to the ion-induced-dipole attraction between the reactants. Scaled Landau-Zener calculations presented here identify a transfer plus excitation channel which has the correct energy dependence at low energies. This finding suggest the need for a comprehensive coupled channel calculation which would include such product states. 25 refs., 8 figs

Negative ion molecule reactions of WF6: evidence for a pressure dependent branching ratio

International Nuclear Information System (INIS)

Viggiano, A.A.; Paulson, J.F.

1984-01-01

Rate coefficients have been measured in a selected ion flow tube (SIFT) for reactions of several negative ions with WF 6 . With the exception of SF - 5 , all the reactant ions studied having an electron detachment energy less than 3.36 eV reacted rapidly by charge exchange. SF - 5 transferred a fluoride ion producing WF - 7 . Ions with detachment energies greater than 3.36 eV associated rapidly with WF - 6 . Br - , with a detachment energy of 3.36 eV, reacted with WF 6 both by ion-neutral association and by charge exchange. The branching ratio for these two channels was found to depend on temperature and pressure. All these data indicate that the electron affinity of WF 6 is nearly equal to that of Br

Imaging the interphase of carbon fiber composites using transmission electron microscopy: Preparations by focused ion beam, ion beam etching, and ultramicrotomy

Directory of Open Access Journals (Sweden)

Wu Qing

2015-10-01

Full Text Available Three sample preparation techniques, focused ion beam (FIB, ion beam (IB etching, and ultramicrotomy (UM were used in comparison to analyze the interphase of carbon fiber/epoxy composites using transmission electron microscopy. An intact interphase with a relatively uniform thickness was obtained by FIB, and detailed chemical analysis of the interphase was investigated by electron energy loss spectroscopy. It shows that the interphase region is 200 nm wide with an increasing oxygen-to-carbon ratio from 10% to 19% and an almost constant nitrogen-to-carbon ratio of about 3%. However, gallium implantation of FIB tends to hinder fine structure analysis of the interphase. For IB etching, the interphase region is observed with transition morphology from amorphous resin to nano-crystalline carbon fiber, but the uneven sample thickness brings difficulty for quantitative chemical analysis. Moreover, UM tends to cause damage and/or deformation on the interphase. These results are meaningful for in-depth understanding on the interphase characteristic of carbon fiber composites.

A chemically activated graphene-encapsulated LiFePO4 composite for high-performance lithium ion batteries.

Science.gov (United States)

Ha, Jeonghyun; Park, Seung-Keun; Yu, Seung-Ho; Jin, Aihua; Jang, Byungchul; Bong, Sungyool; Kim, In; Sung, Yung-Eun; Piao, Yuanzhe

2013-09-21

A composite of modified graphene and LiFePO4 has been developed to improve the speed of charging-discharging and the cycling stability of lithium ion batteries using LiFePO4 as a cathode material. Chemically activated graphene (CA-graphene) has been successfully synthesized via activation by KOH. The as-prepared CA-graphene was mixed with LiFePO4 to prepare the composite. Microscopic observation and nitrogen sorption analysis have revealed the surface morphologies of CA-graphene and the CA-graphene/LiFePO4 composite. Electrochemical properties have also been investigated after assembling coin cells with the CA-graphene/LiFePO4 composite as a cathode active material. Interestingly, the CA-graphene/LiFePO4 composite has exhibited better electrochemical properties than the conventional graphene/LiFePO4 composite as well as bare LiFePO4, including exceptional speed of charging-discharging and excellent cycle stability. That is because the CA-graphene in the composite provides abundant porous channels for the diffusion of lithium ions. Moreover, it acts as a conducting network for easy charge transfer and as a divider, preventing the aggregation of LiFePO4 particles. Owing to these properties of CA-graphene, LiFePO4 could demonstrate enhanced and stably long-lasting electrochemical performance.

Method of detecting defects in ion exchange membranes of electrochemical cells by chemochromic sensors

Science.gov (United States)

Brooker, Robert Paul; Mohajeri, Nahid

2016-01-05

A method of detecting defects in membranes such as ion exchange membranes of electrochemical cells. The electrochemical cell includes an assembly having an anode side and a cathode side with the ion exchange membrane in between. In a configuration step a chemochromic sensor is placed above the cathode and flow isolation hardware lateral to the ion exchange membrane which prevents a flow of hydrogen (H.sub.2) between the cathode and anode side. The anode side is exposed to a first reactant fluid including hydrogen. The chemochromic sensor is examined after the exposing for a color change. A color change evidences the ion exchange membrane has at least one defect that permits H.sub.2 transmission therethrough.

Ion transport membrane reactor systems and methods for producing synthesis gas

Science.gov (United States)

Repasky, John Michael

2015-05-12

Embodiments of the present invention provide cost-effective systems and methods for producing a synthesis gas product using a steam reformer system and an ion transport membrane (ITM) reactor having multiple stages, without requiring inter-stage reactant injections. Embodiments of the present invention also provide techniques for compensating for membrane performance degradation and other changes in system operating conditions that negatively affect synthesis gas production.

Dielectric functions, chemical and atomic compositions of the near surface layers of implanted GaAs by In+ ions

Science.gov (United States)

Kulik, M.; Kołodyńska, D.; Bayramov, A.; Drozdziel, A.; Olejniczak, A.; Żuk, J.

2018-06-01

The surfaces of (100) GaAs were irradiated with In+ ions. The implanted samples were isobaric annealed at 800 °C and then of dielectric function, the surface atomic concentrations of atoms and also the chemical composition of the near surface layers in these implanted semiconductor samples were obtained. The following investigation methods were used: spectroscopic ellipsometry (SE), Rutherford backscattering spectrometry analyses (RBSA) and X-ray photoelectron spectroscopy (XPS) in the study of the above mentioned quantities, respectively. The change of the shape spectra of the dielectric functions at about 3.0 eV phonon energy, diffusion of In+ ions as well as chemical composition changes were observed after ion implantation and the thermal treatment. Due to displacement of Ga ions from GaAs by the In+ ions the new chemical compound InAs was formed. The relative amounts Ga2O3 and As2O3 ratio increase in the native oxide layers with the fluences increase after the thermal treatment of the samples. Additionally, it was noticed that the quantities of InO2 increase with the increasing values of the irradiated ions before thermal treatment.

A Combined Thermodynamics & Computational Method to Assess Lithium Composition in Anode and Cathode of Lithium Ion Batteries

International Nuclear Information System (INIS)

Zhang, Wenyu; Jiang, Lianlian; Van Durmen, Pauline; Saadat, Somaye; Yazami, Rachid

2016-01-01

With aim to address the open question of accurate determination of lithium composition in anode and cathode at a defined state of charge (SOC) of lithium ion batteries (LIB), we developed a method combining electrochemical thermodynamic measurements (ETM) and computational data fitting protocol. It is a common knowledge that in a lithium ion battery the SOC of anode and cathode differ from the SOC of the full-cell. Differences are in large part due to irreversible lithium losses within cell and to electrode mass unbalance. This implies that the lithium composition range in anode and in cathode during full charge and discharge cycle in full-cell is different from the composition range achieved in lithium half-cells of anode and cathode over their respective full SOC ranges. To the authors knowledge there is no unequivocal and practical method to determine the actual lithium composition of electrodes in a LIB, hence their SOC. Yet, accurate lithium composition assessment is fundamental not only for understanding the physics of electrodes but also for optimizing cell performances, particularly energy density and cycle life.

Microstructure and mechanical properties of CVI carbon fiber/SiC composites

International Nuclear Information System (INIS)

Noda, T.; Araki, H.; Abe, F.; Okada, M.

1992-01-01

Microstructures and mechanical properties of carbon fiber/SiC composites prepared with chemical vapor infiltration (CVI) were examined to optimize the process conditions such as reactant and infiltration temperature. Ethyl-trichloro-silane (ETS) and methyl-trichloro-silane (MTS) were used as a source of SiC. CVI was conducted for 108 ks at maximum under a pressure of 13.3 kPa at 1273-1573 K. The composite with a density higher than 80% was obtained at 1373-1423 K and 1423-1374 K from ETS and MTS, respectively. The main matrix formed was β SiC for both reactants. However, silicon also deposited in SiC matrix for MTS. Preferential wettability of SiC to the carbon fiber was observed, and graphite was detected in the interface between the matrix and the carbon fiber by TEM. Mechanical properties were evaluated by bend tests at room temperature. High strength of around 800 MPa was obtained for the composites if the thickness of the surface coated layer was less than 50 μm. Apparent fracture thoughness of the present carbon fiber/SiC composite was 6-10 MPa m 1/2 at room temperature. (orig.)

Determination of isotopic composition of uranium in microparticles by secondary ion mass spectrometry

International Nuclear Information System (INIS)

Veniaminov, N.N.; Kolesnikov, O.N.; Stebel'kov, V.A.

1992-01-01

Aerosol particles including uranium in their composition are specific atmospheric polutants. Uranium is used as nuclear fuel in atomic power stations and in spacecraft power units, and also as a component of nuclear warheads. In order to monitor the discharge of uranium-containing aerosol particles to the atmosphere, they must first be identified. As an example, one may cite an investigation of the elemental composition and radioactivity of particles formed in the accident at the Chernobyl atomic power station. One of the most informative indicators of the origin of uranium-containing aerosol particles is the isotopic composition of the uranium. Secondary ion mass spectrometry (SIMS) offers unique possibilities for the measurement of isotope ratios in individual microscopic objects. At the same time, a measurement of isotope ratios of sulfur in microsection of galenite PbS 2 has shown that the application of SIMS for these purposes is seriously limited by the difference in yield of secondary ions for isotopes with different masses. These discrimination effects, in the case of light elements such as boron, may result in distortion of the isotope ratios by several percent. In the case of heavy elements, however, the effect is less significant, amounting to about 0.5% for lead isotopes. 13 refs., 3 figs., 1 tab

Fabrication of flower-like tin/carbon composite microspheres as long-lasting anode materials for lithium ion batteries

Energy Technology Data Exchange (ETDEWEB)

Kang, Tae-Woo [Department of Chemical Engineering, College of Engineering, Hanyang University, Seoul, 133-791 (Korea, Republic of); Lim, Hyung-Seok [Department of WCU Engineering, College of Engineering, Hanyang University, Seoul, 133-791 (Korea, Republic of); Park, Seong-Jin [Department of Chemical Engineering, College of Engineering, Hanyang University, Seoul, 133-791 (Korea, Republic of); Sun, Yang-Kook [Department of WCU Engineering, College of Engineering, Hanyang University, Seoul, 133-791 (Korea, Republic of); Suh, Kyung-Do, E-mail: kdsuh@hanyang.ac.kr [Department of Chemical Engineering, College of Engineering, Hanyang University, Seoul, 133-791 (Korea, Republic of)

2017-01-01

In this work, we report the fabrication of the flower-like tin/carbon (Sn/C) composite microspheres using sulfonated semi-interpenetrating polystyrene (SPS) microspheres as a carbon precursor. The sulfonation degree of SPS has great effects on the resulting particle size, morphology, amount of introduced Sn, and the carbonization yield of the microspheres after heat treatment. The obtained Sn/C composite microspheres were characterized by scanning electron microscopy (SEM), focused-ion beam SEM, and X-ray diffraction. The flower-like Sn/C composite electrodes exhibited higher charge-discharge capacities than those of graphite as an anode material for a lithium ion battery. In addition, they show a long lasting cyclability, even through 400 cycles. - Highlights: • Tin nanocrystals are introduced in flower-like carbon spheres with many ripples. • Long lasting cyclability is exhibited at 1 C rate up to 400 cycles. • Tin content of composite spheres depends on chemical treatment of polymer microspheres.

Silver effect of Co–Ni composite material on energy storage and structural behavior for Li-ion batteries

International Nuclear Information System (INIS)

Gnanamuthu, RM.; Prasanna, K.; Subburaj, T.; Jo, Yong Nam; Lee, Chang Woo

2013-01-01

Ag powder has been comparatively applied to the Co–Ni materials preparing by mixing method and the prepared electrodes were used as negative electrodes for Li-ion batteries applications. The prepared Co–Ni and Ag–Co–Ni with 10 wt.% of Ag composite electrodes are characterized by XRD, FE-SEM with EDX, impedance and electrochemical charge-discharge studies. These electrochemical studies are demonstrated at current rates of 0.1 C and 0.5 C between 0.01 and 2.0 V vs. Li/Li + . The porous Co–Ni and Ag–Co–Ni composite materials are electrochemically tested in lithium half cells. The porous Ag–Co–Ni composite material demonstrates that the initial and end of discharge capacity up to 20th cycles is, respectively, 860 and 715 mAh g −1 at 0.1 C rate maintaining at approximately 83%. The porous Ag–Co–Ni composite electrode may be a good candidate for high power lithium-ion batteries.

Remote sensing of electron density and ion composition using nonducted whistler observations on OGO 1 and Van Allen Probes

Science.gov (United States)

Sonwalkar, V. S.; Butler, J.; Reddy, A.

2017-12-01

We present a new method to remotely measure magnetospheric electron density and ion composition using lightning generated nonducted whistlers observed on a satellite. Electron and ion densities play important roles in magnetospheric processes such as wave-particle interactions in the equatorial region and ion-neutral dynamics in the ionosphere, and are important for calculating space weather effects such as particle precipitation, GPS scintillations, and satellite drag. The nonducted whistler resulting from a single lightning appears on a spectrogram as a series of magnetospherically reflected traces with characteristic dispersion (time delay versus frequency) and upper and lower cut off frequencies. Ray tracing simulations show that these observed characteristics depend on the magnetospheric electron density and ion composition. The cut off frequencies depend on both electron density and ion composition. The dispersion depends strongly on electron density, but weakly on ion composition. Using an iterative process to fit the measured dispersion and cutoff frequencies to those obtained from ray tracing simulations, it is possible to construct the electron and ion density profiles of the magnetosphere. We demonstrate our method by applying it to nonducted whistlers observed on OGO 1 and Van Allen probe satellites. In one instance (08 Nov 1965), whistler traces observed on OGO 1 (L = 2.4, λm = -6°) displayed a few seconds of dispersion and cutoff frequencies in the 1-10 kHz range. Ray tracing analysis showed that a diffusive equilibrium density model with the following parameters can reproduce the observed characteristics of the whistler traces: 1900 el/cc at L=2.4 and the equator, 358,000 el/cc at F2 peak (hmF2 = 220 km), the relative ion concentrations αH+ = 0.2, αHe+ = 0.2, and αO+ = 0.6 at 1000 km, and temperature 1600 K. The method developed here can be applied to whistlers observed on the past, current, and future magnetospheric satellite missions carrying

Low energy ion scattering as a tool for surface structure and composition analysis

International Nuclear Information System (INIS)

Armour, D.G.

1980-01-01

Low energy ion scattering is finding increasing application in the study of areas such as gas adsorption, thin film deposition and surface damage creation and annealing during ion irradiation where structural and compositional changes occurring in only the outermost atomic layer need to be monitored. The capabilities of the technique and the ways in which it has been developed for different types of analysis depend strongly on the fundamental atomic collision processes taking place at the surface and it is these processes, together with examples of their role in analysis applications, that form the subject of this paper. (author)

Studies of local degradation phenomena in composite cathodes for lithium-ion batteries

International Nuclear Information System (INIS)

Kerlau, Marie; Marcinek, Marek; Srinivasan, Venkat; Kostecki, Robert M.

2007-01-01

LiNi 0.8 Co 0.15 Al 0.05 O 2 and LiNi 1/3 Co 1/3 Mn 1/3 O 2 composite cathodes were cycled in model cells to study interfacial phenomena that could lead to electrode degradation. Ex situ spectroscopic analysis of the tested cathodes, which suffered substantial power and capacity loss, showed that the state of charge (SOC) of oxide particles on the cathode surface was highly non-uniform despite the deep discharge of the Li-ion cell at the end of the test. The inconsistent kinetic behavior of individual oxide particles was attributed to the degradation of electronic pathways within the composite cathodes. A simple theoretical model based on a distributed network showed that an increase of the contact resistance between composite electrode particles may be responsible for non-uniform local kinetic behavior of individual oxide particles and the overall degradation of electrochemical performance of composite electrodes

Ejection of Coulomb Crystals from a Linear Paul Ion Trap for Ion-Molecule Reaction Studies.

Science.gov (United States)

Meyer, K A E; Pollum, L L; Petralia, L S; Tauschinsky, A; Rennick, C J; Softley, T P; Heazlewood, B R

2015-12-17

Coulomb crystals are being increasingly employed as a highly localized source of cold ions for the study of ion-molecule chemical reactions. To extend the scope of reactions that can be studied in Coulomb crystals-from simple reactions involving laser-cooled atomic ions, to more complex systems where molecular reactants give rise to multiple product channels-sensitive product detection methodologies are required. The use of a digital ion trap (DIT) and a new damped cosine trap (DCT) are described, which facilitate the ejection of Coulomb-crystallized ions onto an external detector for the recording of time-of-flight (TOF) mass spectra. This enables the examination of reaction dynamics and kinetics between Coulomb-crystallized ions and neutral molecules: ionic products are typically cotrapped, thus ejecting the crystal onto an external detector reveals the masses, identities, and quantities of all ionic species at a selected point in the reaction. Two reaction systems are examined: the reaction of Ca(+) with deuterated isotopologues of water, and the charge exchange between cotrapped Xe(+) with deuterated isotopologues of ammonia. These reactions are examples of two distinct types of experiment, the first involving direct reaction of the laser-cooled ions, and the second involving reaction of sympathetically-cooled heavy ions to form a mixture of light product ions. Extensive simulations are conducted to interpret experimental results and calculate optimal operating parameters, facilitating a comparison between the DIT and DCT approaches. The simulations also demonstrate a correlation between crystal shape and image shape on the detector, suggesting a possible means for determining crystal geometry for nonfluorescing ions.

Development of methodics for the characterization of the composition of the ion-collision-induced secondary-particle flux by comparison of the yield contributions of photoinduced ion formation processes

International Nuclear Information System (INIS)

Vering, Guido

2008-01-01

The aim of this work was to develop a method to distinguish between different ion formation processes and to determine the influence of these processes on the total number of detected monatomic ions of a certain element. A vector/matrix-formalism was developed, which describes the physical processes of sputtering, ion formation, mass separation and detection in laser-SNMS. In the framework of the method developed, based on this theoretic formalism, changes in the secondary flux contribution of the respective element were observed by comparing the detected monatomic ion yield obtained in specifically aligned (SIMS and) laser-SNMS experiments. The yields resulting from these experiments were used to calculate characteristic numbers to compare the flux composition from different surfaces. The potential of the method was demonstrated for the elements boron, iron and gadolinium by investigating the changes in the flux composition of secondary particles sputtered from metallic surfaces, as a function of the oxygen concentration at the surface. Finally, combined laser-SNMS depth profiles and images, obtained with both laser systems, were presented to demonstrate how the parallel detection of the three differently originated ion signals of the same element can be used to get additional information about the composition of the flux of secondary particles synchronously during the analysis of elemental distributions. In this respect the presented method can be a very helpful tool to prevent misleading interpretations of SIMS or laser-SNMS data. (orig.)

Proton-bound cluster ions in ion mobility spectrometry

Science.gov (United States)

Ewing, R. G.; Eiceman, G. A.; Stone, J. A.

1999-01-01

Gaseous oxygen and nitrogen bases, both singly and as binary mixtures, have been introduced into ion mobility spectrometers to study the appearance of protonated molecules, and proton-bound dimers and trimers. At ambient temperature it was possible to simultaneously observe, following the introduction of molecule A, comparable intensities of peaks ascribable to the reactant ion (H2O)nH+, the protonated molecule AH+ and AH+ H2O, and the symmetrical proton bound dimer A2H+. Mass spectral identification confirmed the identifications and also showed that the majority of the protonated molecules were hydrated and that the proton-bound dimers were hydrated to a much lesser extent. No significant peaks ascribable to proton-bound trimers were obtained no matter how high the sample concentration. Binary mixtures containing molecules A and B, in some cases gave not only the peaks unique to the individual compounds but also peaks due to asymmetrical proton bound dimers AHB+. Such ions were always present in the spectra of mixtures of oxygen bases but were not observed for several mixtures of oxygen and nitrogen bases. The dimers, which were not observable, notable for their low hydrogen bond strengths, must have decomposed in their passage from the ion source to the detector, i.e. in a time less than approximately 5 ms. When the temperature was lowered to -20 degrees C, trimers, both homogeneous and mixed, were observed with mixtures of alcohols. The importance of hydrogen bond energy, and hence operating temperature, in determining the degree of solvation of the ions that will be observed in an ion mobility spectrometer is stressed. The possibility is discussed that a displacement reaction involving ambient water plays a role in the dissociation.

Study of chloride ion transport of composite by using cement and starch as a binder

Energy Technology Data Exchange (ETDEWEB)

Armynah, Bidayatul; Halide, Halmar; Zahrawani,; Reski, Nurhadi; Tahir, Dahlang, E-mail: dtahir@fmipa.unhas.ac.id [Department of Physics, Hasanuddin University, Makassar 90245 Indonesia (Indonesia)

2016-03-11

This study presents the chemical bonding and the structural properties of composites from accelerator chloride test migration (ACTM). The volume fractions between binder (cement and starch) and charcoal in composites are 20:80 and 60:40. The effect of the binder to the chemical composition, chemical bonding, and structural properties before and after chloride ion passing through the composites was determined by X-ray fluorescence (XRF), by Fourier transform infra-red (FTIR), and x-ray diffraction (XRD), respectively. From the XRD data, XRF data, and the FTIR data shows the amount of chemical composition, the type of binding, and the structure of composites are depending on the type of binder. The amount of chloride migration using starch as binder is higher than that of cement as a binder due to the density effects.

Colorimetric detection and removal of radioactive Co ions using sodium alginate-based composite beads

International Nuclear Information System (INIS)

Kim, Daigeun; Jo, Ara; Yang, Hee-Man; Seo, Bum-Kyoung; Lee, Kune-Woo; Lee, Taek Seung

2017-01-01

Highlights: • Organic/inorganic hybridized alginate beads were newly synthesized via sol-gel chemistry. • Interaction between the azopyridine and metal ion is the main cause of Co ion detection. • The beads showed improved stability and least leakage of azopyridine during use. • Removal of Co ion was assessed by the ion-exchange of carboxylate groups in alginate. • The beads with dual functions of detection and removal of Co ion were successfully accomplished. - Abstract: We demonstrate a simple method for the visual determination and removal of Co ions using a bead-shaped, capturing probe based on hybridized sodium alginate. For Co ions, the designed protocol consisted of three main constituents: an azopyridine-based Co ion-probe for visual detection; sodium alginate as an adsorbent for the Co ion and a bead construct for removal and structure; silica as a linker for the probe and the alginate, leading to a robust structure. When the composite beads were exposed to Co ions, the yellow color of the beads turned to intensive violet and the color intensity was associated with the Co ion concentration. The color variation was quantified using red-green-blue (RGB) color values that were obtained with a scanner and evaluated with Photoshop. The technique achieved both visual recognition with obvious color change of the beads and efficient removal of the radioactive 60 Co ion. The sensing and removal of any radioactive isotope could be achieved with an appropriate sensing probe, to provide a simple and universal platform for remediation.

Colorimetric detection and removal of radioactive Co ions using sodium alginate-based composite beads

Energy Technology Data Exchange (ETDEWEB)

Kim, Daigeun; Jo, Ara [Organic and Optoelectronic Materials Laboratory, Department of Organic Materials Engineering, Chungnam National University, Daejeon 34134 (Korea, Republic of); Yang, Hee-Man; Seo, Bum-Kyoung; Lee, Kune-Woo [Decontamination and Decommissioning Research Division, Korea Atomic Energy Research Institute, Daejeon 34057 (Korea, Republic of); Lee, Taek Seung, E-mail: tslee@cnu.ac.kr [Organic and Optoelectronic Materials Laboratory, Department of Organic Materials Engineering, Chungnam National University, Daejeon 34134 (Korea, Republic of)

2017-03-15

Highlights: • Organic/inorganic hybridized alginate beads were newly synthesized via sol-gel chemistry. • Interaction between the azopyridine and metal ion is the main cause of Co ion detection. • The beads showed improved stability and least leakage of azopyridine during use. • Removal of Co ion was assessed by the ion-exchange of carboxylate groups in alginate. • The beads with dual functions of detection and removal of Co ion were successfully accomplished. - Abstract: We demonstrate a simple method for the visual determination and removal of Co ions using a bead-shaped, capturing probe based on hybridized sodium alginate. For Co ions, the designed protocol consisted of three main constituents: an azopyridine-based Co ion-probe for visual detection; sodium alginate as an adsorbent for the Co ion and a bead construct for removal and structure; silica as a linker for the probe and the alginate, leading to a robust structure. When the composite beads were exposed to Co ions, the yellow color of the beads turned to intensive violet and the color intensity was associated with the Co ion concentration. The color variation was quantified using red-green-blue (RGB) color values that were obtained with a scanner and evaluated with Photoshop. The technique achieved both visual recognition with obvious color change of the beads and efficient removal of the radioactive {sup 60}Co ion. The sensing and removal of any radioactive isotope could be achieved with an appropriate sensing probe, to provide a simple and universal platform for remediation.

Formation and decomposition of ammoniated ammonium ions

International Nuclear Information System (INIS)

Ikezoe, Yasumasa; Suzuki, Kazuya; Nakashima, Mikio; Yokoyama, Atsushi; Shiraishi, Hirotsugu; Ohno, Shin-ichi

1998-09-01

Structures, frequencies, and chemical reactions of ammoniated ammonium ions (NH 4 + .nNH 3 ) were investigated theoretically by ab initio molecular orbital calculations and experimentally by observing their formation and decomposition in a corona discharge-jet expansion process. The ab initio calculations were carried out using a Gaussian 94 program, which gave optimized structures, binding energies and harmonic vibrational frequencies of NH 4 + .nNH 3 . Effects of discharge current, the reactant gas and the diameter of the gas expanding pinhole were examined on the size n distribution of NH 4 + .nNH 3 . The results indicated that the cluster ion, in the jet expansion process, grew in size mostly equal to or less than one unit under experimental conditions employed. Effects of discharge current, pinhole diameter, flight time in vacuum and cluster size were examined on the decomposition rate of cluster ions formed. In our experimental conditions, the internal energies of cluster ions were mainly determined through exo- and/or endo-thermic reactions involved in the cluster formation process. (author)

The effect of correlations on the entropy and hadrochemical composition in heavy ion reactions

International Nuclear Information System (INIS)

Barz, H.-W.; Biro, T.S.; Lukacs, B.; Zimanyi, J.

1987-01-01

It is shown that spatial correlations between the constituent particles of a gas lead to roughly excluded volume type corrections in the equation of state. These corrections will appreciably change the hadrochemical composition of fireballs formed in heavy ion reactions. (author) 29 refs.; 3 figs

Three-dimensional iron sulfide-carbon interlocked graphene composites for high-performance sodium-ion storage

DEFF Research Database (Denmark)

Huang, Wei; Sun, Hongyu; Shangguan, Huihui

2018-01-01

Three-dimensional (3D) carbon-wrapped iron sulfide interlocked graphene (Fe7S8@C-G) composites for high-performance sodium-ion storage are designed and produced through electrostatic interactions and subsequent sulfurization. The iron-based metal–organic frameworks (MOFs, MIL-88-Fe) interact with...

Changes in phase composition and stress state of surface layers of VK20 hard alloy after ion bombardment

International Nuclear Information System (INIS)

Platonov, G.L.; Leonov, E.Yu.; Anikin, V.N.; Anikeev, A.I.

1988-01-01

Titanium ion bombardment of the surface of the hard VK20 alloy is studied for its effect on variations in the phase and chemical composition of its surface layers. It is stated that ion treatment results in the appearance of the η-phase of Co 6 W 6 C composition in the surface layer of the VK20 alloy, in the increase of distortions and decrease of coherent scattering blocks of the hard alloy carbide phase. Such a bombardment is found to provoke a transition of the plane-stressed state of the hard alloy surface into the volume-stressed state. It is established that ion treatment does not cause an allotropic transition of the cobalt phase α-modification, formed during grinding of the hard alloy, into the β-modification

Teachers' Misconceptions about the Effects of Addition of More Reactants or Products on Chemical Equilibrium

Science.gov (United States)

Cheung, Derek; Ma, Hong-jia; Yang, Jie

2009-01-01

The importance of research on misconceptions about chemical equilibrium is well recognized by educators, but in the past, researchers' interest has centered on student misconceptions and has neglected teacher misconceptions. Focusing on the effects of adding more reactants or products on chemical equilibrium, this article discusses the various…

In-flight calibration of satellite ion composition data using artificial intelligence methods

International Nuclear Information System (INIS)

Waldemark, J.

1995-11-01

The scope of this report is to evaluate some of the cognitive analyzing techniques that are available and that might be useful for calibration, validation and data analysis of a satellite measurement system. As an example, these cognitive techniques are used to perform a post launch calibration of the three-dimensional ion composition, TICS, on the Freja satellite. 17 refs, 28 figs, 6 tabs

Physico-Chemical and Electrochemical Properties of Nanoparticulate NiO/C Composites for High Performance Lithium and Sodium Ion Battery Anodes

Directory of Open Access Journals (Sweden)

Amaia Iturrondobeitia

2017-12-01

Full Text Available Nanoparticulate NiO and NiO/C composites with different carbon proportions have been prepared for anode application in lithium and sodium ion batteries. Structural characterization demonstrated the presence of metallic Ni in the composites. Morphological study revealed that the NiO and Ni nanoparticles were well dispersed in the matrix of amorphous carbon. The electrochemical study showed that the lithium ion batteries (LIBs, containing composites with carbon, have promising electrochemical performances, delivering specific discharge capacities of 550 mAh/g after operating for 100 cycles at 1C. These excellent results could be explained by the homogeneity of particle size and structure, as well as the uniform distribution of NiO/Ni nanoparticles in the in situ generated amorphous carbon matrix. On the other hand, the sodium ion battery (NIB with the NiO/C composite revealed a poor cycling stability. Post-mortem analyses revealed that this fact could be ascribed to the absence of a stable Solid Electrolyte Interface (SEI or passivation layer upon cycling.

Measurements of ion temperature and plasma hydrogenic composition by collective Thomson scattering in neutral beam heated discharges at TEXTOR

DEFF Research Database (Denmark)

Stejner Pedersen, Morten; Salewski, Mirko; Korsholm, Søren Bang

2013-01-01

A method is developed to perform plasma composition and ion temperature measurements across the plasma minor radius in TEXTOR based on ion cyclotron structures in collective Thomson scattering spectra. By gradually moving the scattering volume, we obtain measurements across the outer midplane of ...

Carbon Cryogel Silicon Composite Anode Materials for Lithium Ion Batteries

Science.gov (United States)

Woodworth James; Baldwin, Richard; Bennett, William

2010-01-01

A variety of materials are under investigation for use as anode materials in lithium-ion batteries, of which, the most promising are those containing silicon. 10 One such material is a composite formed via the dispersion of silicon in a resorcinol-formaldehyde (RF) gel followed by pyrolysis. Two silicon-carbon composite materials, carbon microspheres and nanofoams produced from nano-phase silicon impregnated RF gel precursors have been synthesized and investigated. Carbon microspheres are produced by forming the silicon-containing RF gel into microspheres whereas carbon nano-foams are produced by impregnating carbon fiber paper with the silicon containing RF gel to create a free standing electrode. 1-4,9 Both materials have demonstrated their ability to function as anodes and utilize the silicon present in the material. Stable reversible capacities above 400 mAh/g for the bulk material and above 1000 mAh/g of Si have been observed.

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

International Nuclear Information System (INIS)

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

2015-01-01

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

Ion-conductive properties of polyether-based composite electrolytes filled with mesoporous silica, alumina and titania

International Nuclear Information System (INIS)

Tominaga, Yoichi; Endo, Masanori

2013-01-01

Composite polymer electrolytes were prepared consisting of amorphous polyether, Li salt and mesoporous inorganic filler, and we investigated their ion-conductive properties. We synthesized three types of filler, mesoporous silica, alumina and titania (MP-Si, Al, Ti), and characterized their structural and physicochemical properties using SEM, TEM, SAXS and BET surface area measurements. From these measurements, we confirmed that MP fillers have well-defined arrays of mesoporous and hexagonal structures. Dependence on the MP filler content of the glass transition temperature (T g ) revealed that the addition of filler to original polyether-salt electrolyte causes T g decrease, to due to the dissociation of aggregated ions such as triples or crystalline complex domains. The MP-Ti composites had the greatest ionic conductivity (1.4 × 10 −5 S/cm, 7.5 wt% at 30 °C) of all samples, and the values were more than double that of the original. The addition of MP-Ti also increased the lithium transference number, because the electrolyte/filler interface provided active sites that increase mobile Li ions and conducting paths so as to enhance the mobility

Spherical nanostructured Si/C composite prepared by spray drying technique for lithium ion batteries anode

Energy Technology Data Exchange (ETDEWEB)

Chen Libao [Energy Science and Technology Laboratory, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050 (China); Graduate School of Chinese Academy of Sciences, Beijing 100049 (China); Xie Xiaohua [Energy Science and Technology Laboratory, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050 (China); Graduate School of Chinese Academy of Sciences, Beijing 100049 (China); Wang Baofeng [Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); Wang Ke [Energy Science and Technology Laboratory, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050 (China); Xie Jingying [Energy Science and Technology Laboratory, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050 (China) and Graduate School of Chinese Academy of Sciences, Beijing 100049 (China)]. E-mail: jyxie@mail.sim.ac.cn

2006-07-15

Spherical nanostructured Si/C composite was prepared by spray drying technique, followed by heat treatment, in which nanosized silicon and fine graphite particles were homogeneously embedded in carbon matrix pyrolyzed by phenol formaldehyde resin. Cyclic voltammetry tests showed two pairs of redox peaks corresponding to lithiation and delithiation of Si/C composite. The Si/C composite exhibited a reversible capacity of 635 mAh g{sup -1} and good cycle performance used in lithium ion batteries. To improve cycle performance of this Si/C composite further, the carbon-coated Si/C composite was synthesized by the second spray drying and heat treatment processing. The cycle performance of carbon-coated Si/C composite was improved significantly, which was attributed to the formation of stable SEI passivation layers on the outer surface of carbon shell which protected the bared silicon from exposing to electrolyte directly.

Spherical nanostructured Si/C composite prepared by spray drying technique for lithium ion batteries anode

International Nuclear Information System (INIS)

Chen Libao; Xie Xiaohua; Wang Baofeng; Wang Ke; Xie Jingying

2006-01-01

Spherical nanostructured Si/C composite was prepared by spray drying technique, followed by heat treatment, in which nanosized silicon and fine graphite particles were homogeneously embedded in carbon matrix pyrolyzed by phenol formaldehyde resin. Cyclic voltammetry tests showed two pairs of redox peaks corresponding to lithiation and delithiation of Si/C composite. The Si/C composite exhibited a reversible capacity of 635 mAh g -1 and good cycle performance used in lithium ion batteries. To improve cycle performance of this Si/C composite further, the carbon-coated Si/C composite was synthesized by the second spray drying and heat treatment processing. The cycle performance of carbon-coated Si/C composite was improved significantly, which was attributed to the formation of stable SEI passivation layers on the outer surface of carbon shell which protected the bared silicon from exposing to electrolyte directly

Morphology variation, composition alteration and microstructure changes in ion-irradiated 1060 aluminum alloy

Science.gov (United States)

Wan, Hao; Si, Naichao; Wang, Quan; Zhao, Zhenjiang

2018-02-01

Morphology variation, composition alteration and microstructure changes in 1060 aluminum irradiated with 50 keV helium ions were characterized by field emission scanning electron microscopy (FESEM) equipped with x-ray elemental scanning, 3D measuring laser microscope and transmission electron microscope (TEM). The results show that, helium ions irradiation induced surface damage and Si-rich aggregates in the surfaces of irradiated samples. Increasing the dose of irradiation, more damages and Si-rich aggregates would be produced. Besides, defects such as dislocations, dislocation loops and dislocation walls were the primary defects in the ion implanted layer. The forming of surface damages were related with preferentially sputtering of Al component. While irradiation-enhanced diffusion and irradiation-induced segregation resulted in the aggregation of impurity atoms. And the aggregation ability of impurity atoms were discussed based on the atomic radius, displacement energy, lattice binding energy and surface binding energy.

Nanostructure Sn-Co-C composite lithium ion battery electrode with unique stability and high electrochemical performance

International Nuclear Information System (INIS)

Li Mengyuan; Liu Chunling; Shi Meirong; Dong Wensheng

2011-01-01

Nanostructure Sn-Co-C composites with different compositions are synthesized by a simple solution polymerization using inexpensive raw materials followed by pyrolysis in nitrogen atmosphere. The nanostructure Sn-Co-C composites are characterized using various analytic techniques. The results show that the electrochemical performances of the composites are strongly dependent on their structure and composition. Among these composites the Sn-Co-C-1 with a weight composition of Sn 0.31 Co 0.09 C 0.6 exhibits high reversible capacity and excellent cycleability when used as an anode for rechargeable lithium ion batteries. This composite is composed of SnCo 2 , SnCo, Sn and amorphous carbon, and the nanoparticles of SnCo 2 , SnCo and Sn are uniformly dispersed into the amorphous carbon matrix, the average diameter of these metal nanoparticles is 8.44 nm.

The Generation of Dehydroalanine Residues in Protonated Polypeptides: Ion/Ion Reactions for Introducing Selective Cleavages

Science.gov (United States)

Peng, Zhou; Bu, Jiexun; McLuckey, Scott A.

2017-09-01

We examine a gas-phase approach for converting a subset of amino acid residues in polypeptide cations to dehydroalanine (Dha). Subsequent activation of the modified polypeptide ions gives rise to specific cleavage N-terminal to the Dha residue. This process allows for the incorporation of selective cleavages in the structural characterization of polypeptide ions. An ion/ion reaction within the mass spectrometer between a multiply protonated polypeptide and the sulfate radical anion introduces a radical site into the multiply protonated polypeptide reactant. Subsequent collisional activation of the polypeptide radical cation gives rise to radical side chain loss from one of several particular amino acid side chains (e.g., leucine, asparagine, lysine, glutamine, and glutamic acid) to yield a Dha residue. The Dha residues facilitate preferential backbone cleavages to produce signature c- and z-ions, demonstrated with cations derived from melittin, mechano growth factor (MGF), and ubiquitin. The efficiencies for radical side chain loss and for subsequent generation of specific c- and z-ions have been examined as functions of precursor ion charge state and activation conditions using cations of ubiquitin as a model for a small protein. It is noted that these efficiencies are not strongly dependent on ion trap collisional activation conditions but are sensitive to precursor ion charge state. Moderate to low charge states show the greatest overall yields for the specific Dha cleavages, whereas small molecule losses (e.g., water/ammonia) dominate at the lowest charge states and proton catalyzed amide bond cleavages that give rise to b- and y-ions tend to dominate at high charge states. [Figure not available: see fulltext.

Ion plasma deposition of oxide films with graded-stoichiometry composition: Experiment and simulation

Science.gov (United States)

Volpyas, V. A.; Tumarkin, A. V.; Mikhailov, A. K.; Kozyrev, A. B.; Platonov, R. A.

2016-07-01

A method of ion plasma deposition is proposed for obtaining thin multicomponent films with continuously graded composition in depth of the film. The desired composition-depth profile is obtained by varying the working gas pressure during deposition in the presence of an additional adsorbing screen in the drift space between a sputtered target and substrate. Efficiency of the proposed method is confirmed by Monte Carlo simulation of the deposition of thin films of Ba x Sr1- x TiO3 (BSTO) solid solution. It is demonstrated that, during sputtering of a Ba0.3Sr0.7TiO3 target, the parameter of composition stoichiometry in the growing BSTO film varies in the interval of x = 0.3-0.65 when the gas pressure is changed within 2-60 Pa.

Analysis of abused drugs by selected ion monitoring: quantitative comparison of electron impact and chemical ionization

International Nuclear Information System (INIS)

Foltz, R.L.; Knowlton, D.A.; Lin, D.C.K.; Fentiman, A.F. Jr.

1975-01-01

A comparison was made of the relative sensitivities of electron impact and chemical ionization when used for selected ion monitoring analysis of commonly abused drugs. For most of the drugs examined chemical ionization using ammonia as the reactant gas gave the largest single m/e ion current response per unit weight of sample. However, if maximum sensitivity is desired it is important to evaluate electron impact and chemical ionization with respect to both maximum response and degree of interference from background and endogenous materials

Adsorption behavior of carboxylated cellulose nanocrystal—polyethyleneimine composite for removal of Cr(VI) ions

Energy Technology Data Exchange (ETDEWEB)

Liu, Chao; Jin, Ru-Na; Ouyang, Xiao-kun, E-mail: xkouyang@zjou.edu.cn; Wang, Yang-Guang

2017-06-30

Highlights: • A carboxylated cellulose nanocrystal-polyethyleneimine composite (CCN-PEI) was prepared. • The as-prepared CCN-PEI was characterized by SEM, TEM, FT-IR, and XPS. • Results suggested that the reusable CCN-PEI could remove Cr(VI) from aqueous solutions with a high adsorption capacity. • The adsorption isotherm, thermodynamics, and kinetics of the adsorption process are also discussed. - Abstract: In this study, a composite adsorbent (CCN-PEI) composed of carboxylated cellulose nanocrystals (CCN) and polyethyleneimine (PEI) was prepared through an amidation reaction between the carboxyl groups of the CCN and the amine groups of the PEI. The adsorption performance of the CCN-PEI was tested by removing Cr(VI) ions from aqueous solutions. The physicochemical properties of the CCN and the Cr(VI) ion-loaded CCN-PEI were studied using scanning electron microscopy (SEM), transmission electron microscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. To investigate the adsorption kinetics of Cr(VI) ions onto this newly developed CCN-PEI, we performed experiments under different adsorption conditions, by varying the contact time, solution pH, initial Cr(VI) ion concentration, and adsorption temperature. The prepared CCN-PEI exhibited an encouraging uptake capacity of 358.42 mg × g{sup −1}. The adsorption process was fast: within the first 100 min, Cr(VI) ion adsorption onto the CCN-PEI was about 65%, and the adsorption equilibrium was reached within 250 min. Kinetics experiments indicated that the adsorption process could be described by a pseudo-second-order kinetic model. Furthermore, our adsorption equilibrium data fit the Langmuir isotherms well. The calculated thermodynamic parameters, such as the free energy change (ΔG = −2.93 kJ × mol{sup −1}), enthalpy change (ΔH = −5.69 kJ × mol{sup −1}), and entropy change (ΔS = −9.14 kJ × mol{sup −1}), indicate that the adsorption of Cr(VI) ions onto CCN

Preparation of SiO2-KCoFC composite ion-exchanger for removal of Cs in the soil decontamination waste solution

International Nuclear Information System (INIS)

Lee, Jung Joon; Moon, Jei kwon; Lee, Kune Woo

2009-01-01

The soil decontamination process has been developed for remediate the soil wastes excavated from the TRIGA research reactor sites. Even though the process was proven to be very effective for decontaminate the radioactive nuclides such as cesium and cobalt, the secondary spent solution should be treated with an appropriate method to minimize the waste volume. There are mainly two components in the spent decontamination solution of Cs and Co. The Co in the waste solution can be removed easily by precipitation under a basic condition. However, since the Cs is hardly removed by precipitation, an appropriate selective removal method should be employed. In this study, an inorganic composite ion exchanger of SiO 2 -KCoFC was prepared by sol-gel method for a removal of Cs in the decontamination waste solution. An optimum condition for a preparation of the composite ion exchanger and the adsorption performances of the prepared composite ion exchangers were evaluated

The influence of tertiary butyl hydrazine as a co-reactant on the atomic layer deposition of silver

Energy Technology Data Exchange (ETDEWEB)

Golrokhi, Zahra; Marshall, Paul A.; Romani, Simon [Centre for Materials and Structures, School of Engineering,The University of Liverpool, Liverpool L69 3GH (United Kingdom); Rushworth, Simon [EpiValence, The Wilton Centre, Redcar, Cleveland, TS10 4RF (United Kingdom); Chalker, Paul R. [Centre for Materials and Structures, School of Engineering,The University of Liverpool, Liverpool L69 3GH (United Kingdom); Potter, Richard J., E-mail: rjpott@liverpool.ac.uk [Centre for Materials and Structures, School of Engineering,The University of Liverpool, Liverpool L69 3GH (United Kingdom)

2017-03-31

Highlights: • We demonstrate metallic silver growth by direct liquid injection thermal ALD. • A substituted hydrazine is used as a powerful reducing agent for the first time. • The hydrazine extends the ALD temperature window compared with alcohol. • Hydrazine promotes a more planar growth mode compared to alcohol. • Film adhesion is improved using hydrazine compared with alcohol. - Abstract: Ultra-thin conformal silver films are the focus of development for applications such as anti-microbial surfaces, optical components and electronic devices. In this study, metallic silver films have been deposited using direct liquid injection thermal atomic layer deposition (ALD) using (hfac)Ag(1,5-COD) ((hexafluoroacetylacetonato)silver(I)(1,5-cyclooctadiene)) as the metal source and tertiary butyl hydrazine (TBH) as a co-reactant. The process provides a 23 °C wide ‘self-limiting’ ALD temperature window between 105 and 128 °C, which is significantly wider than is achievable using alcohol as a co-reactant. A mass deposition rate of ∼20 ng/cm{sup 2}/cycle (∼0.18 Å/cycle) is observed under self-limiting growth conditions. The resulting films are crystalline metallic silver with a near planar film-like morphology which are electrically conductive. By extending the temperature range of the ALD window by the use of TBH as a co-reactant, it is envisaged that the process will be exploitable in a range of new low temperature applications.

Comparison of a new global empirical ion composition model with available satellite data

Czech Academy of Sciences Publication Activity Database

Truhlík, Vladimír; Třísková, Ludmila; Šmilauer, Jan; Iwamoto, I.

2003-01-01

Roč. 31, č. 3 (2003), s. 665-675 ISSN 0273-1177 R&D Projects: GA ČR GP205/02/P037; GA AV ČR IAA3042201; GA AV ČR IAB3042104 Institutional research plan: CEZ:AV0Z3042911 Keywords : satellite data * ion composition model * outer ionosphere Subject RIV: DG - Athmosphere Sciences, Meteorology Impact factor: 0.483, year: 2003

High Performance Li4Ti5O12/Si Composite Anodes for Li-Ion Batteries

Directory of Open Access Journals (Sweden)

Chunhui Chen

2015-08-01

Full Text Available Improving the energy capacity of spinel Li4Ti5O12 (LTO is very important to utilize it as a high-performance Li-ion battery (LIB electrode. In this work, LTO/Si composites with different weight ratios were prepared and tested as anodes. The anodic and cathodic peaks from both LTO and silicon were apparent in the composites, indicating that each component was active upon Li+ insertion and extraction. The composites with higher Si contents (LTO:Si = 35:35 exhibited superior specific capacity (1004 mAh·g−1 at lower current densities (0.22 A·g−1 but the capacity deteriorated at higher current densities. On the other hand, the electrodes with moderate Si contents (LTO:Si = 50:20 were able to deliver stable capacity (100 mAh·g−1 with good cycling performance, even at a very high current density of 7 A·g−1. The improvement in specific capacity and rate performance was a direct result of the synergy between LTO and Si; the former can alleviate the stresses from volumetric changes in Si upon cycling, while Si can add to the capacity of the composite. Therefore, it has been demonstrated that the addition of Si and concentration optimization is an easy yet an effective way to produce high performance LTO-based electrodes for lithium-ion batteries.

Effect of Reactant Concentration on the Microstructure of SiC Nano wires Grown In Situ within SiC Fiber Preforms

International Nuclear Information System (INIS)

Kim, Weon Ju; Kang, Seok Min; Park, Ji Yeon; Ryu, Woo Seog

2006-01-01

Silicon carbide fiber-reinforced silicon carbide matrix (SiC f /SiC) composites are considered as advanced materials for control rods and other in-core components of high-temperature gas cooled reactors. Although the carbon fiber-reinforced carbon matrix (C f /C) composites are more mature and have advantages in cost, manufacturability and some thermomechanical properties, the SiC f /SiC composites have a clear advantage in irradiation stability, specifically a lower level of swelling and retention of mechanical properties. This offers a lifetime component for control rod application to HTGRs while the Cf/C composites would require 2-3 replacements over the reactor lifetime. In general, the chemical vapor infiltration (CVI) technique has been used most widely to produce SiC f /SiC composites. Although the technique produces a highly pure SiC matrix, it requires a long processing time and inevitably contains large interbundle pores. The present authors have recently developed 'whisker growing-assisted process,' in which one-dimensional SiC nano structures with high aspect ratios such as whiskers, nano wires and nano rods are introduced into the fiber preform before the matrix infiltration step. This novel method can produce SiC f /SiC composites with a lower porosity and an uniform distribution of pores when compared with the conventional CVI. This would be expected to increase mechanical and thermal properties of the SiC f /SiC composites. In order to take full advantage of the whisker growing strategy, however, a homogeneous growth of long whiskers is required. In this study, we applied the atmospheric pressure CVI process without metallic catalysts for the growth of SiC nano wires within stacked SiC fiber fabrics. We focused on the effect of the concentration of a reactant gas on the growth behavior and microstructures of the SiC nano wires and discussed a controlling condition for the homogenous growth of long SiC nano wires

Ion conducting polymers and polymer blends for alkali metal ion batteries

Science.gov (United States)

DeSimone, Joseph M.; Pandya, Ashish; Wong, Dominica; Vitale, Alessandra

2017-08-29

Electrolyte compositions for batteries such as lithium ion and lithium air batteries are described. In some embodiments the compositions are liquid compositions comprising (a) a homogeneous solvent system, said solvent system comprising a perfluropolyether (PFPE) and polyethylene oxide (PEO); and (b) an alkali metal salt dissolved in said solvent system. In other embodiments the compositions are solid electrolyte compositions comprising: (a) a solid polymer, said polymer comprising a crosslinked product of a crosslinkable perfluropolyether (PFPE) and a crosslinkable polyethylene oxide (PEO); and (b) an alkali metal ion salt dissolved in said polymer. Batteries containing such compositions as electrolytes are also described.

Free-standing and bendable carbon nanotubes/TiO2 nanofibres composite electrodes for flexible lithium ion batteries

International Nuclear Information System (INIS)

Zhang, Peng; Qiu, Jingxia; Zheng, Zhanfeng; Liu, Gao; Ling, Min; Martens, Wayde; Wang, Haihui; Zhao, Huijun; Zhang, Shanqing

2013-01-01

Carbon nanotube (CNT) and TiO 2 nanofibre composite films are prepared and used as anode materials for lithium ion batteries (LIBs) without the use of binders and conventional copper current collector. The preliminary experimental results from X-ray diffraction, scanning electron microscopy and transmission electron microscopy suggest that the TiO 2 nanofibres were well-dispersed and interwoven by the CNTs, forming freestanding, bendable and light weighted composite. In comparison with TiO 2 nanofibre based LIBs, the CNTs could significantly improve the battery performance due to their high conductivity property and 3D network morphology. In both 1–3 V and 0.01–3 V testing voltage ranges, the as-prepared composites show excellent reversible capacity and capacity retention. The superior lithium storage capacity of the CNT/TiO 2 composite was mainly attributed to dual functions of the CNTs – the CNTs not only provide conductive networks to assist the electron transfer but also facilitate lithium ion diffusion between the electrolyte and the TiO 2 active materials by preventing agglomeration of TiO 2 nanofibres. This work demonstrates that the CNT–TiO 2 composite film could be one type of potential electrode material for large-scale LIB applications

Ion-molecule reactions in the binary mixture of ethylene oxide and trioxane, 1

International Nuclear Information System (INIS)

Kumakura, Minoru; Sugiura, Toshio.

1977-01-01

The formation mechanism of protonated molecular ions by cross-reactions in ethylene oxide-trioxane mixtures has been studied with use of a modified time-of-flight mass spectrometer. The precursors of the product ions were determined by analysis of the fine structure of their ionization efficiency curves using deuterated ethylene oxide. Protonated ethylene oxide is formed by the hydrogen atom transfer reaction of ethylene oxide molecular ion with trioxane, and protonated trioxane by the proton transfer reaction of CHO + (from ethylene oxide) with trioxane. In the ion-molecule reactions of ethylene-d 4 oxide-trioxane mixtures, appreciable isotope effect was observed. The CHO + from ethylene oxide is an important reactant ion as compared with that from trioxane in the proton transfer reaction, and CHO + from ethylene oxide was suggested as a thermal reactive ion. The order of proton affinity could be estimated from the proton transfer reactions involving CHO + . It was found that the proton affinity of trioxane is smaller than that of ethylene oxide. (auth.)

Electron capture by Ne3+ ions from atomic hydrogen

International Nuclear Information System (INIS)

Rejoub, R.; Bannister, M.E.; Havener, C.C.; Savin, D.W.; Verzani, C.J.; Wang, J.G.; Stancil, P.C.

2004-01-01

Using the Oak Ridge National Laboratory ion-atom merged-beam apparatus, absolute total electron-capture cross sections have been measured for collisions of Ne 3+ ions with hydrogen (deuterium) atoms at energies between 0.07 and 826 eV/u. Comparison to previous measurements shows large discrepancies between 50 and 400 eV/u. Previously published molecular-orbital close-coupling (MOCC) calculations were performed over limited energy ranges, but show good agreement with the present measurements. Here MOCC calculations are presented for energies between 0.01 and 1000 eV/u for collisions with both H and D. For energies below ∼1 eV/u, an enhancement in the magnitude of both the experimental and theoretical cross sections is observed which is attributed to the ion-induced dipole attraction between the reactants. Below ∼4 eV/u, the present calculations show a significant target isotope effect

Electron capture by Ne3+ ions from atomic hydrogen

Science.gov (United States)

Rejoub, R.; Bannister, M. E.; Havener, C. C.; Savin, D. W.; Verzani, C. J.; Wang, J. G.; Stancil, P. C.

2004-05-01

Using the Oak Ridge National Laboratory ion-atom merged-beam apparatus, absolute total electron-capture cross sections have been measured for collisions of Ne3+ ions with hydrogen (deuterium) atoms at energies between 0.07 and 826 eV/u . Comparison to previous measurements shows large discrepancies between 50 and 400 eV/u . Previously published molecular-orbital close-coupling (MOCC) calculations were performed over limited energy ranges, but show good agreement with the present measurements. Here MOCC calculations are presented for energies between 0.01 and 1000 eV/u for collisions with both H and D. For energies below ˜1 eV/u , an enhancement in the magnitude of both the experimental and theoretical cross sections is observed which is attributed to the ion-induced dipole attraction between the reactants. Below ˜4 eV/u , the present calculations show a significant target isotope effect.

The Magnetic Properties of Metal-Alloy Glass Composites Prepared by Ion Implantation

International Nuclear Information System (INIS)

Julian Fernandez, Cesar de; Mattei, Giovanni; Sada, Cinzia; Maurizio, Chiara; Padovani, Sara; Mazzoldi, Paolo; Sangregorio, Claudio; Gatteschi, Dante

2003-01-01

The structural and magnetic properties of Co-Ni, Co-Fe and Ni-Cu alloy nanoparticles formed in silica matrix by sequential ion implantation are presented. These nanoparticles show crystal structure similar to the corresponding bulk alloys. In the Co-Ni and Co-Fe, magnetization saturation and coercive field depend on the the alloy composition, crystal structure and size effects. Ferromagnetic resonance studies show that collective magnetic processes are present and these are determined by the film-like morphology of the implanted region. The temperature dependence of the magnetization of the NixCu100-x samples indicates that their Curie Temperatures are larger than the corresponding bulk ones. This feature is discussed considering the composition of the nanoparticles and the size effects

Study on performance of composite polymer films doped with modified molecular sieve for lithium-ion batteries

International Nuclear Information System (INIS)

Zhang Yuqing; Zhang Guodong; Du Tingdong; Zhang Lizao

2010-01-01

To improve the tensile strength and ionic conductivity of composite polymer films for lithium-ion batteries, molecular sieves of MCM-41 modified with sulfated zirconia (SO 4 2- /ZrO 2 , SZ), denoted as MCM-41/SZ, were doped into a poly(vinylidene fluoride) (PVdF) matrix to fabricate MCM-41/SZ composite polymer films, denoted as MCM-41/SZ films. Examination by transmission electron microscope (TEM) shows that modified molecular sieves have lower aggregation and a more porous structure. Tensile strength tests were carried out to investigate the mechanical performance of MCM-41/SZ films, and then the electrochemical performance of batteries with MCM-41/SZ films as separators was tested. The results show that the tensile strength (σ t ) of MCM-41/SZ film was up to 7.8 MPa; the ionic conductivity of MCM-41/SZ film was close to 10 -3 S cm -1 at room temperature; and the coulombic efficiency of the assembled lithium-ion battery was 92% at the first cycle and reached as high as 99.99% after the 20th cycle. Meanwhile, the charge-discharge voltage plateau of the lithium-ion battery presented a stable state. Therefore, MCM-41/SZ films are a good choice as separators for lithium-ion batteries due to their high tensile strength and ionic conductivity.

Swift heavy ion irradiation induced phase transformation in undoped and niobium doped titanium dioxide composite thin films

Energy Technology Data Exchange (ETDEWEB)

Gautam, Subodh K., E-mail: subodhkgtm@gmail.com [Inter University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110 067 (India); Chettah, Abdelhak [LGMM Laboratory, Université 20 Août 1955-Skikda, BP 26, 21000 Skikda (Algeria); Singh, R.G. [Department of Physics, Bhagini Nivedita College, Delhi University, Delhi 110043 (India); Ojha, Sunil; Singh, Fouran [Inter University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110 067 (India)

2016-07-15

Study reports the effect of swift heavy ion (SHI) irradiation induced phase transformation in undoped and Niobium doped anatase TiO{sub 2} composite thin films. Investigations were carried out at different densities of electronic excitations (EEs) using 120 MeV Ag and 130 MeV Ni ions irradiations. Films were initially annealed at 900 °C and results revealed that undoped films were highly stable in anatase phase, while the Nb doped films showed the composite nature with the weak presence of Niobium penta-oxide (Nb{sub 2}O{sub 5}) phase. The effect at low density of EEs in undoped film show partial anatase to rutile phase transformation; however doped film shows only further growth of Nb{sub 2}O{sub 5} phase beside the anatase to rutile phase transformation. At higher density of EEs induced by Ag ions, registered continuous ion track of ∼3 nm in lattice which leads to nano-crystallization followed by decomposition/amorphization of rutile TiO{sub 2} and Nb{sub 2}O{sub 5} phases in undoped and doped films, respectively. However, Ni ions are only induced discontinuous sequence of ion tracks with creation of damage and disorder and do not show amorphization in the lattice. The in-elastic thermal spike calculations were carried out for anatase TiO{sub 2} phase to understand the effect of EEs on anatase to rutile phase transformation followed by amorphization in NTO films in terms of continuous and discontinuous track formation by SHI irradiation.

Anodic behaviour of the stainless steel AISI 430 in aqueous solutions of chloride and sulphate ions

International Nuclear Information System (INIS)

Sebrao, M.Z.

1982-01-01

The kinetics of the dissolution of stainless steel AISI 430 in the presence of chloride and sulphate ions has been studied in terms of the ion concentration, the pH variation, and the velocity of the working electrode. The experimental method utilized was the potentiostatic anodic polarization, and the reactants used were NaCl and Na 2 SO 4 at room temperature. Atomic Absorption spectrophotometry and Auger Electrons spectroscopy (AES) analyses were made in order to support the interpretation of results obtained by means of the potentiostatic polarization method. (author)

Surface plasmon resonance sensing detection of mercury and lead ions based on conducting polymer composite.

Directory of Open Access Journals (Sweden)

Mahnaz M Abdi

Full Text Available A new sensing area for a sensor based on surface plasmon resonance (SPR was fabricated to detect trace amounts of mercury and lead ions. The gold surface used for SPR measurements were modified with polypyrrole-chitosan (PPy-CHI conducting polymer composite. The polymer layer was deposited on the gold surface by electrodeposition. This optical sensor was used for monitoring toxic metal ions with and without sensitivity enhancement by chitosan in water samples. The higher amounts of resonance angle unit (ΔRU were obtained for PPy-CHI film due to a specific binding of chitosan with Pb(2+ and Hg(2+ ions. The Pb(2+ ion bind to the polymer films most strongly, and the sensor was more sensitive to Pb(2+ compared to Hg(2+. The concentrations of ions in the parts per million range produced the changes in the SPR angle minimum in the region of 0.03 to 0.07. Data analysis was done by Matlab software using Fresnel formula for multilayer system.

Staged membrane oxidation reactor system

Science.gov (United States)

Repasky, John Michael; Carolan, Michael Francis; Stein, VanEric Edward; Chen, Christopher Ming-Poh

2012-09-11

Ion transport membrane oxidation system comprising (a) two or more membrane oxidation stages, each stage comprising a reactant zone, an oxidant zone, one or more ion transport membranes separating the reactant zone from the oxidant zone, a reactant gas inlet region, a reactant gas outlet region, an oxidant gas inlet region, and an oxidant gas outlet region; (b) an interstage reactant gas flow path disposed between each pair of membrane oxidation stages and adapted to place the reactant gas outlet region of a first stage of the pair in flow communication with the reactant gas inlet region of a second stage of the pair; and (c) one or more reactant interstage feed gas lines, each line being in flow communication with any interstage reactant gas flow path or with the reactant zone of any membrane oxidation stage receiving interstage reactant gas.

Use of periodic variations of reactant concentrations in time resolved ftir studies of CO oxidation on Pd/ZrO{sub 2} catalysts

Energy Technology Data Exchange (ETDEWEB)

Ortelli, E; Wokaun, A [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

1999-08-01

Sine wave modulation of feed concentrations was used to induce dynamic variations in the concentrations of products, intermediates and reactants, which were monitored in a diffuse reflectance FTIR (DRIFT) cell. The phase shift {Delta}{phi} between the external perturbation of the feed and the signals of products, intermediates and reactants was examined in dependence on the modulation frequency {omega}. Reaction constants of a simplified model mechanism were estimated for a Pd{sub 25}Zr{sub 75} based catalyst for CO oxidation. (author) 1 fig., 2 refs.

Microwave Derived Facile Approach to Sn/Graphene Composite Anodes for, Lithium-Ion Batteries

International Nuclear Information System (INIS)

Beck, Faith R.; Epur, Rigved; Hong, Daeho; Manivannan, Ayyakkannu; Kumta, Prashant N.

2014-01-01

Graphical abstract: Tin particles embedded in graphene (G) sheet have been synthesized by microwave reduction of tin halide (SnCl 2 ) and graphite oxide (GO) followed by annealing in argon. The microwave reaction resulted in the formation of tin oxide embedded in graphene sheets. Annealing in argon at elevated temperatures initiated carbothermal reduction culminating in the formation of tin decorated graphene sheet composites that were employed as anodes for lithium-ion batteries. X-ray diffraction analysis of the final composite showed the presence of crystalline tin combined with a very small diffraction peak corresponding to (002) plane of graphite. Scanning electron microscopy (SEM) revealed decorated graphene layers with tin droplets. X-ray Photoelectron Spectroscopy (XPS) confirmed the presence of graphene and graphene oxide in the composite. Electrochemical cycling response indicated that the tin/graphene composite exhibited initial discharge capacities varying from 790 mAh/g to 850 mAh/g depending on the composition, while a stable reversible capacity of ∼500 mAh/g was achieved for optimized compositions when cycled at a current density of ∼100 mA/g in the voltage window of 0.02 to 1.2 V vs. Li + /Li. Carbon coating of the Sn/G composite ultimately achieved by decomposition of dextrose using microwave heating significantly improved the electrochemical cycling stability. - Highlights: • Tin embedded graphene sheets have been synthesized by microwave reduction. • Tin oxide and graphene formed was carbothermally reduced to Sn/graphene. • XPS confirmed presence of graphene and graphene oxide in the composite. • Electrochemical response indicated capacities in 790 mAh/g to 850 mAh/g range. • Carbon coated composite yielded stable reversible capacity ∼500 mAh/g. - Abstract: Tin particles embedded in graphene (G) sheets have been synthesized by microwave reduction of tin halide (SnCl 2 .2H 2 O) and graphite oxide (GO) followed by annealing in argon

Second generation PMR polyimide/fiber composites

Science.gov (United States)

Cavano, P. J.

1979-01-01

A second generation polymerization monomeric reactants (PMR) polyimdes matrix system (PMR 2) was characterized in both neat resin and composite form with two different graphite fiber reinforcements. Three different formulated molecular weight levels of laboratory prepared PMR 2 were examined, in addition to a purchased experimental fully formulated PMR 2 precurser solution. Isothermal aging of graphite fibers, neat resin samples and composite specimens in air at 316 C were investigated. Humidity exposures at 65 C and 97 percent relative humidity were conducted for both neat resin and composites for eight day periods. Anaerobic char of neat resin and fire testing of composites were conducted with PMR 15, PMR 2, and an epoxy system. Composites were fire tested on a burner rig developed for this program. Results indicate that neat PMR 2 resins exhibit excellent isothermal resistance and that PMR 2 composite properties appear to be influenced by the thermo-oxidative stability of the reinforcing fiber.

Compositional and structural studies of ion-beam modified AlN/TiN multilayers

Energy Technology Data Exchange (ETDEWEB)

Amati, M., E-mail: matteo.amati@elettra.eu [Elettra – Sincrotrone Trieste SCpA,Area Science Park, 34149, Trieste (Italy); Gregoratti, L.; Sezen, H. [Elettra – Sincrotrone Trieste SCpA,Area Science Park, 34149, Trieste (Italy); Grce, A.; Milosavljević, M. [VINČA Institute of Nuclear Sciences, Belgrade University, P.O. Box 522, 11001, Belgrade (Serbia); Homewood, K.P. [Materials Research Institute and School of Physics and Astronomy, Queen Mary University of London, Mile End Road, E1 4NS, London (United Kingdom)

2017-07-31

Highlights: • Inter-layer mixing, atomic redistribution, structural change, and phase transformation on AlN/TiN multilayers via argon ion irradiation. • Severe modifications are observed with TEM studies on highly immiscible alternating layers without any side effects such as beam heating. • The original TiN layers appear to grow in thickness by consuming the adjacent AlN layers, while obtaining a better TiAlN fcc crystalline structure. • Photoemission spectroscopy/microscopy indicates a transformation into Al deficient ternary and highly homogeneous compounds on both layers. • These results can be interesting towards further development of radiation tolerant materials based on immiscible ceramic nanocomposites. - Abstract: This paper reports on compositional and structural modifications induced in coated AlN/TiN multilayers by argon ion irradiation. The initial structure consisting of totally 30 alternate AlN (8 nm thick) and TiN (9.3 nm thick) layers was deposited on Si (100) wafers, by reactive sputtering. Irradiation was done with 180 keV Ar{sup +} to a high dose of 8 × 10{sup 16} ions/cm{sup 2}, which introduces up to ∼10 at.% of argon species, and generates a maximum displacement per atom of 92 for AlN and 127 for TiN, around the projected ion range (109 ± 34 nm). Characterizations were performed by Rutherford backscattering spectrometry, spatially resolved x-ray photoelectron spectroscopy, and transmission electron microscopy. The obtained results reveal that this highly immiscible and thermally stable system suffered a severe modification upon the applied ion irradiation, although it was performed at room temperature. They illustrate a thorough inter-layer mixing, atomic redistribution, structural change and phase transformation within the affected depth. The original TiN layers appear to grow in thickness, consuming the adjacent AlN layers, while retaining the fcc crystalline structure. In the mostly affected region, the interaction proceeds

Surface composition of biomedical components by ion beam analysis

International Nuclear Information System (INIS)

Kenny, M.J.; Wielunski, L.S.; Baxter, G.R.

1991-01-01

Materials used for replacement body parts must satisfy a number of requirements such as biocompatibility and mechanical ability to handle the task with regard to strength, wear and durability. When using a CVD coated carbon fibre reinforced carbon ball, the surface must be ion implanted with uniform dose of nitrogen ions in order to make it wear resistant. The mechanism by which the wear resistance is improved is one of radiation damage and the required dose of about 10 16 cm -2 can have a tolerance of about 20%. To implant a spherical surface requires manipulation of the sample within the beam and control system (either computer or manually operated) to enable uniform dose all the way from polar to equatorial regions on the surface. A manipulator has been designed and built for this purpose. In order to establish whether the dose is uniform, nuclear reaction analysis using the reaction 14 N(d,α) 12 C is an ideal method of profiling. By taking measurements at a number of points on the surface, the uniformity of nitrogen dose can be ascertained. It is concluded that both Rutherford Backscattering and Nuclear Reaction Analysis can be used for rapid analysis of surface composition of carbon based materials used for replacement body components. 2 refs., 2 figs

Ion-beam-induced topography and compositional changes in depth profiling

International Nuclear Information System (INIS)

Carter, G.; Nobes, M.J.

1992-01-01

When energetic ions penetrate and stop in solids they not only add a new atomic constituent to the matrix but they also create atomic recoils and defects. The fluxes of these entities can give rise to spatial redistribution of atomic components, which may be partly or completely balanced by reordering and relaxation processes. These latter, in turn, may be influenced by fields and gradients induced by the primary relocation processes and by the energy deposited. These will include quasi-thermal, concentration (or chemical potential) and electrostatic gradients and may act to enhance or suppress atomic redistribution. Some, or all, of these processes will operate, depending upon the system under study, when energetic ions are employed to sputter erode a substrate for depth sectioning and, quite generally, can perturb the atomic depth profile that it is intended to evaluate. Theoretical and computational approaches to modelling such processes will be outlined and experimental examples shown which illustrate specific phenomena. In particular the accumulation of implant species and defect generation or redistribution can modify, with increasing ion fluence, the local sputtering mechanism and create further problems in depth profile analysis as a changing surface topography penetrates the solid. Examples of such topographic evolution and its influence on depth profiling analysis will be given and models to explain general and specific behaviour will be outlined. The commonality of models which examine both depth-dependent composition modification and surface topography evolution will be stressed. (author)

Product ion isotopologue pattern: A tool to improve the reliability of elemental composition elucidations of unknown compounds in complex matrices.

Science.gov (United States)

Kaufmann, A; Walker, S; Mol, G

2016-04-15

Elucidation of the elemental compositions of unknown compounds (e.g., in metabolomics) generally relies on the availability of accurate masses and isotopic ratios. This study focuses on the information provided by the abundance ratio within a product ion pair (monoisotopic versus the first isotopic peak) when isolating and fragmenting the first isotopic ion (first isotopic mass spectrum) of the precursor. This process relies on the capability of the quadrupole within the Q Orbitrap instrument to isolate a very narrow mass window. Selecting only the first isotopic peak (first isotopic mass spectrum) leads to the observation of a unique product ion pair. The lighter ion within such an isotopologue pair is monoisotopic, while the heavier ion contains a single carbon isotope. The observed abundance ratio is governed by the percentage of carbon atoms lost during the fragmentation and can be described by a hypergeometric distribution. The observed carbon isotopologue abundance ratio (product ion isotopologue pattern) gives reliable information regarding the percentage of carbon atoms lost in the fragmentation process. It therefore facilitates the elucidation of the involved precursor and product ions. Unlike conventional isotopic abundances, the product ion isotopologue pattern is hardly affected by isobaric interferences. Furthermore, the appearance of these pairs greatly aids in cleaning up a 'matrix-contaminated' product ion spectrum. The product ion isotopologue pattern is a valuable tool for structural elucidation. It increases confidence in results and permits structural elucidations for heavier ions. This tool is also very useful in elucidating the elemental composition of product ions. Such information is highly valued in the field of multi-residue analysis, where the accurate mass of product ions is required for the confirmation process. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

Si clusters/defective graphene composites as Li-ion batteries anode materials: A density functional study

International Nuclear Information System (INIS)

Li, Meng; Liu, Yue-Jie; Zhao, Jing-xiang; Wang, Xiao-guang

2015-01-01

Highlights: • We study the interaction between Si clusters with pristine and defective graphene. • We find that the binding strength of Si clusters on graphene can be enhanced to different degrees after introducing various defects. • It is found that both graphene and Si cluster in the Si/graphene composites can preserve their Li uptake ability. - Abstract: Recently, the Si/graphene hybrid composites have attracted considerable attention due to their potential application for Li-ion batteries. How to effectively anchor Si clusters to graphene substrates to ensure their stability is an important factor to determine their performance for Li-ion batteries. In the present work, we have performed comprehensive density functional theory (DFT) calculations to investigate the geometric structures, stability, and electronic properties of the deposited Si clusters on defective graphenes as well as their potential applications for Li-ion batteries. The results indicate that the interfacial bonding between these Si clusters with the pristine graphene is quietly weak with a small adsorption energy (<−0.21 eV). Due to the presence of vacancy site, the binding strength of Si clusters on defective graphene is much stronger than that of pristine one, accompanying with a certain amount of charge transfer from Si clusters to graphene substrates. Moreover, the ability of Si/graphene hybrids for Li uptake is studied by calculating the adsorption of Li atoms. We find that both graphenes and Si clusters in the Si/graphene composites preserve their Li uptake ability, indicating that graphenes not only server as buffer materials for accommodating the expansion of Si cluster, but also provide additional intercalation sites for Li

60 keV Ar⁺-ion induced modification of microstructural, compositional, and vibrational properties of InSb

Energy Technology Data Exchange (ETDEWEB)

Datta, D. P.; Garg, S. K.; Som, T., E-mail: tsom@iopb.res.in [SUNAG Laboratory, Institute of Physics, Bhubaneswar, Odisha 751005 (India); Satpati, B. [Surface Physics and Materials Science Division, Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata 700064 (India); Sahoo, P. K. [School of Physical Sciences, National Institute of Science Education and Research, Bhubaneswar 751005, Odisha (India); Kanjilal, A. [Department of Physics, Shiv Nadar University, Uttar Pradesh 203207 (India); Dhara, S. [Surface and Nanoscience Division, Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102 (India); Kanjilal, D. [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India)

2014-10-14

Room temperature irradiation of InSb(111) by 60 keV Ar⁺-ions at normal (0°) and oblique (60°) angles of incidence led to the formation of nanoporous structure in the high fluence regime of 1×10¹⁷ to 3×10¹⁸ ions cm⁻². While a porous layer comprising of a network of interconnected nanofibers was generated by normal ion incidence, evolution of plate-like structures was observed for obliquely incident ions. Systematic studies of composition and structure using energy dispersive x-ray spectroscopy, Raman spectroscopy, x-ray photoelectron spectroscopy, Raman mapping, grazing incidence x-ray diffraction, and cross-sectional transmission electron microscopy revealed a high degree of oxidation of the ion-induced microstructures with the presence of In₂O₃ and Sb₂O₃ phases and presence of nanocrystallites within the nanoporous structures. The observed structural evolution was understood in terms of processes driven by ion-induced defect accumulation within InSb.

Stress analysis in cylindrical composition-gradient electrodes of lithium-ion battery

Science.gov (United States)

Zhong, Yaotian; Liu, Yulan; Wang, B.

2017-07-01

In recent years, the composition-gradient electrode material has been verified to be one of the most promising materials in lithium-ion battery. To investigate diffusion-induced stresses (DIS) generated in a cylindrical composition-gradient electrode, the finite deformation theory and the stress-induced diffusion hypothesis are adopted to establish the constitutive equations. Compared with stress distributions in a homogeneous electrode, the increasing forms of Young's modulus E(R) and partial molar volume Ω(R) from the electrode center to the surface along the radial direction drastically increase the maximal magnitudes of hoop and axial stresses, while both of the decreasing forms are able to make the stress fields smaller and flatter. Also, it is found that the slope of -1 for E(R) with that of -0.5 for Ω(R) is a preferable strategy to prevent the inhomogeneous electrode from cracking, while for the sake of protecting the electrode from compression failure, the optimal slope for inhomogeneous E(R) and the preferential one for Ω(R) are both -0.5. The results provide a theoretical guidance for the design of composition-gradient electrode materials.

Cross-linked Composite Gel Polymer Electrolyte using Mesoporous Methacrylate-Functionalized SiO2 Nanoparticles for Lithium-Ion Polymer Batteries

Science.gov (United States)

Shin, Won-Kyung; Cho, Jinhyun; Kannan, Aravindaraj G.; Lee, Yoon-Sung; Kim, Dong-Won

2016-01-01

Liquid electrolytes composed of lithium salt in a mixture of organic solvents have been widely used for lithium-ion batteries. However, the high flammability of the organic solvents can lead to thermal runaway and explosions if the system is accidentally subjected to a short circuit or experiences local overheating. In this work, a cross-linked composite gel polymer electrolyte was prepared and applied to lithium-ion polymer cells as a safer and more reliable electrolyte. Mesoporous SiO2 nanoparticles containing reactive methacrylate groups as cross-linking sites were synthesized and dispersed into the fibrous polyacrylonitrile membrane. They directly reacted with gel electrolyte precursors containing tri(ethylene glycol) diacrylate, resulting in the formation of a cross-linked composite gel polymer electrolyte with high ionic conductivity and favorable interfacial characteristics. The mesoporous SiO2 particles also served as HF scavengers to reduce the HF content in the electrolyte at high temperature. As a result, the cycling performance of the lithium-ion polymer cells with cross-linked composite gel polymer electrolytes employing methacrylate-functionalized mesoporous SiO2 nanoparticles was remarkably improved at elevated temperatures. PMID:27189842

Potential application of microporous structured poly(vinylidene fluoride-hexafluoropropylene)/poly(ethylene terephthalate) composite nonwoven separators to high-voltage and high-power lithium-ion batteries

International Nuclear Information System (INIS)

Jeong, Hyun-Seok; Choi, Eun-Sun; Kim, Jong Hun; Lee, Sang-Young

2011-01-01

Highlights: → Microporous-structured PVdF-HFP/PET composite nonwoven separators for Li-batteries. → Well-developed microporous structure and liquid electrolyte wettability. → Provision of facile ion transport and suppressed growth of cell impedance. → Superior cell performance at high-voltages/high-current densities. - Abstract: We demonstrate potential application of a new composite non-woven separator, which is comprised of a phase inversion-controlled, microporous polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP) gel polymer electrolyte and a polyethylene terephthalate (PET) non-woven support, to high-voltage and high-power lithium-ion batteries. In comparison to a commercialized polyethylene (PE) separator, the composite non-woven separator exhibits distinct improvements in microporous structure and liquid electrolyte wettability. Based on the understanding of the composite non-woven separator, cell performances of the separator at challenging charge/discharge conditions are investigated and discussed in terms of ion transport of the separator and AC impedance of the cell. The aforementioned advantageous features of the composite non-woven separator play a key role in providing facile ion transport and suppressing growth of cell impedance during cycling, which in turn contribute to superior cell performances at harsh charge/discharge conditions such as high voltages and high current densities.

Electrospun polyacrylonitrile/polyurethane composite nanofibrous separator with electrochemical performance for high power lithium ion batteries

Energy Technology Data Exchange (ETDEWEB)

Zainab, Ghazala [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Wang, Xianfeng, E-mail: wxf@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Key Laboratory of High Performance Fibers & Products, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Nanofibers Research Center, Modern Textile Institute, Donghua University, Shanghai 200051 (China); Yu, Jianyong [Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Key Laboratory of High Performance Fibers & Products, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Nanofibers Research Center, Modern Textile Institute, Donghua University, Shanghai 200051 (China); Zhai, Yunyun; Ahmed Babar, Aijaz; Xiao, Ke [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Ding, Bin, E-mail: binding@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Key Laboratory of High Performance Fibers & Products, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Nanofibers Research Center, Modern Textile Institute, Donghua University, Shanghai 200051 (China)

2016-10-01

Lithium ion batteries (LIBs) for high performance require separators with auspicious reliability and safety. Keeping LIBs reliability and safety in view, microporous polyacrylonitrile (PAN)/polyurethane (PU) nonwoven composite separator have been developed by electrospinning technique. The physical, electrochemical and thermal properties of the PAN/PU separator were characterized. Improved ionic conductivity up to 2.07 S cm{sup −1}, high mechanical strength (10.38 MPa) and good anodic stability up to 5.10 V are key outcomes of resultant membranes. Additionally, high thermal stability displaying only 4% dimensional change after 0.5 h long exposure to 170 °C in an oven, which could be valuable addition towards the safety of LIBs. Comparing to commercialized polypropylene based separators, resulting membranes offered improved internal short-circuit protection function, offering better rate capability and enhanced capacity retention under same observation conditions. These fascinating characteristics endow these renewable composite nonwovens as promising separators for high power LIBs battery. - Highlights: • The PAN/PU based separators were prepared by multi-needle electrospinning technique. • The electrospun separators displays good mechanical properties and thermal stability. • These separators exhibit good wettability with liquid electrolyte, high ion conductivity and internal short-circuit protection. • Nanofibrous composite nonwoven possesses stable cyclic performance which give rise to acceptable battery performances.

Compositional disordering of GaAs/AlGaAs multiple quantum wells using ion bombardment at elevated temperatures

International Nuclear Information System (INIS)

Anderson, K.K.; Donnelly, J.P.; Wang, C.A.; Woodhouse, J.D.; Haus, H.A.

1988-01-01

A new method has been developed for compositional mixing of heterostructures by ion bombardment at elevated temperatures. Complete mixing of a 1-μm-thick GaAs/AlGaAs 40-period multiple quantum well layer has been achieved by bombardment with 380 keV Ne + ions for 1 h with the sample at 700 0 C. This temperature is much lower than the annealing temperatures used in other vacancy-enhanced disordering techniques, and even lower temperatures and shorter durations should be possible. Compositional disordering is verified by sputter-profile Auger electron spectroscopy and transmission electron microscopy. Complete mixing is also demonstrated by optical transmission spectra of the disordered material, which exhibit the same band edge as a uniform alloy with the average aluminum mole fraction of the multiple quantum well layer

A New Multiphase Equation of State for Composition B

Energy Technology Data Exchange (ETDEWEB)

Coe, Joshua Damon [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Theoretical Division; Margevicius, Madeline Alma [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Theoretical Division

2016-07-25

We describe the construction of a complete equation of state for the high explosive Composition B in its unreacted (inert) form, as well as chemical equilibrium calculations of its detonation products. The multiphase reactant EOS is of SESAME type, and was calibrated to ambient thermal and mechanical data, the shock initiation experiments of Dattelbaum, et al., and the melt line of trinitrotoluene (TNT).

Development of plasma-treated polypropylene nonwoven-based composites for high-performance lithium-ion battery separators

International Nuclear Information System (INIS)

Li, Xiaofei; He, Jinlin; Wu, Dazhao; Zhang, Mingzu; Meng, Juwen; Ni, Peihong

2015-01-01

Graphical abstract: A composite separator based on plasma-treated fluorinated polypropylene (PP) nonwoven, poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) and SiO 2 nanoparticles exhibiting enhanced thermal stability, ionic conductivity and electrochemical properties. Display Omitted -- Highlights: •Fluorinated segments are introduced on the surface of PP nonwoven through plasma treatment. •The obtained composite separators exhibit better physical and electrochemical properties. •The capacity of half-cell with composite separator keeps above 150 mA h g −1 after 100 charge–discharge cycles. -- Abstract: Separators have drawn substantial attention because of their important role in achieving the safety and good electrochemical performance of lithium-ion batteries. In this study, we report a new type of composite membrane prepared by a combination of fluorinated polypropylene (PP) nonwoven fabric, poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) and SiO 2 nanoparticles. 2, 2, 3, 3, 4, 4, 5, 5-Octafluoropentyl methacrylate (OFPMA) is first grafted on the surface of PP nonwoven by plasma treatment to improve the nonwoven’s adhesion with PVdF-HFP. Two kinds of composite separators have been prepared by using the different PP nonwovens together with PVdF-HFP and SiO 2 nanoparticles. They were separately designated as PHS for commercially raw PP nonwoven system and PHS-n for OFPMA-modified PP nonwoven systems (n means plasma treatment time). The morphology, electrolyte uptake, ionic conductivity and electrochemical properties of the composite separators have been analyzed by scanning electron microscope (SEM) analysis, impedance measurement, charge-discharge cycle and C-rate tests, respectively. The results indicate that PHS-10 composite separator using the modified PP nonwoven treated by plasma for 10 min exhibits much better properties than PHS separator, including an improved mechanical property, thermal stability, electrolyte uptake

Material composition – Pinning strength correlation in Nb thin films with focused ion beam-milled washboard nanostructures

International Nuclear Information System (INIS)

Dobrovolskiy, Oleksandr V.; Begun, Evgeniya; Huth, Michael; Shklovskij, Valerij A.

2013-01-01

Highlights: •We fabricated an array of grooves in Nb films by using focused ion beam milling. •We determined the material composition in different areas of the processed films. •We deduced the pinning activation energies from the magneto-resistivity data. •We obtained the material composition – pinning strength correlation in the processed films. -- Abstract: An analysis of the interrelated changes in the material composition and the pinning strength in nanostructured Nb (1 1 0) thin films is presented. The nanopatterns were prepared by focused ion beam milling of an array of uniaxial grooves. They induce a washboard-like pinning potential landscape for vortices in the mixed state. By applying different magnetic fields, the most likely pinning sites along which the flux lines move through the samples have been selected. By this, either the background isotropic pinning of the pristine film or the enhanced isotropic pinning originating from the nanoprocessing has been probed. The enhanced pinning strength in the processed films has been found to correlate with the content of Ga implanted into the films during the nanopatterning

Material composition – Pinning strength correlation in Nb thin films with focused ion beam-milled washboard nanostructures

Energy Technology Data Exchange (ETDEWEB)

Dobrovolskiy, Oleksandr V., E-mail: Dobrovolskiy@Physik.uni-frankfurt.de [Physikalisches Institut, Goethe-Universität, 60438 Frankfurt am Main (Germany); Physical Department, Kharkiv National University, 61077 Kharkiv (Ukraine); Begun, Evgeniya; Huth, Michael [Physikalisches Institut, Goethe-Universität, 60438 Frankfurt am Main (Germany); Shklovskij, Valerij A. [Physical Department, Kharkiv National University, 61077 Kharkiv (Ukraine); Institute for Theoretical Physics, NSC-KIPT, 61108 Kharkiv (Ukraine)

2013-11-15

Highlights: •We fabricated an array of grooves in Nb films by using focused ion beam milling. •We determined the material composition in different areas of the processed films. •We deduced the pinning activation energies from the magneto-resistivity data. •We obtained the material composition – pinning strength correlation in the processed films. -- Abstract: An analysis of the interrelated changes in the material composition and the pinning strength in nanostructured Nb (1 1 0) thin films is presented. The nanopatterns were prepared by focused ion beam milling of an array of uniaxial grooves. They induce a washboard-like pinning potential landscape for vortices in the mixed state. By applying different magnetic fields, the most likely pinning sites along which the flux lines move through the samples have been selected. By this, either the background isotropic pinning of the pristine film or the enhanced isotropic pinning originating from the nanoprocessing has been probed. The enhanced pinning strength in the processed films has been found to correlate with the content of Ga implanted into the films during the nanopatterning.

Evaluation of structural and optical properties of Ce3+ ions doped (PVA/PVP) composite films for new organic semiconductors

Science.gov (United States)

Ali, F. M.; Kershi, R. M.; Sayed, M. A.; AbouDeif, Y. M.

2018-06-01

Polymer blend films based on Polyvinyl alcohol (PVA)/Poly(vinylpyrrolidone) (PVP) doped with different concentration of cerium ions [(PVA/PVP)-x wt.% Ce3+] (x = 3%, 5%, 10% and 15%) were prepared by the conventional solution casting technique. The characteristics of the prepared polymer composite films were studied using X-ray diffraction (XRD), FT-IR and UV-Vis. spectroscopy. The XRD patterns of the investigated samples revealed a clear reduction on the structural parameters such as crystallinity degree and cluster size D of the doped PVA/PVP blend films compared with the virgin one whereas there is no big difference in the d spacing of the product composite films. Significant changes in FT-IR spectra are observed which reveal an interactions between the cerium ions and PVA/PVP blends. The absorption spectra in the ultraviolet-visible region showed a wide red shift in the fundamental absorption edge of (PVA/PVP)-x wt. % Ce3+ composites. The optical gap Eg gradually decreased from 4.54 eV for the undoped PVA/PVP film to 3.10 eV by increasing Ce3+ ions content. The optical dispersion parameters have been analyzed according to Wemple-Didomenico single oscillator model. The dispersion energy Ed, the single oscillator energy Eo, the average inter-band oscillator wavelength λo and the static refractive index no are strongly affected by cerium ions doping. Cerium ions incorporation in PVA/PVP blend films leads to a significant increase in the refractive index and decrease in the optical gap. These results are likely of great important in varieties of applications including polymer waveguides, organic semiconductors, polymer solar cells and optoelectronics devices.

Composition variations of low energy heavy ions during large solar energetic particle events

Energy Technology Data Exchange (ETDEWEB)

Ho, George C., E-mail: George.Ho@jhuapl.edu; Mason, Glenn M., E-mail: Glenn.Mason@jhuapl.edu [Johns Hopkins University Applied Physics Laboratory, Laurel, MD 20723 (United States)

2016-03-25

The time-intensity profile of large solar energetic particle (SEP) event is well organized by solar longitude as observed at Earth orbit. This is mostly due to different magnetic connection to the shock that is associated with large SEP event propagates from the Sun to the heliosphere. Earlier studies have shown event averaged heavy ion abundance ratios can also vary as a function of solar longitude. It was found that the Fe/O ratio for high energy particle (>10 MeV/nucleon) is higher for those western magnetically well connected events compare to the eastern events as observed at L1 by the Advanced Composition Explorer (ACE) spacecraft. In this paper, we examined the low energy (∼1 MeV/nucleon) heavy ions in 110 isolated SEP events from 2009 to the end of 2014. In addition, the optical and radio signatures for all of our events are identified and when data are available we also located the associated coronal mass ejection (CME) data. Our survey shows a higher Fe/O ratio at events in the well-connected region, while there are no corrections between the event averaged elemental composition with the associated coronal mass ejection speed. This is inconsistent with the higher energy results, but inline with other recent low-energy measurements.

Fe3O4/C composite with hollow spheres in porous 3D-nanostructure as anode material for the lithium-ion batteries

Science.gov (United States)

Yang, Zhao; Su, Danyang; Yang, Jinping; Wang, Jing

2017-09-01

3d transition-metal oxides, especially Fe3O4, as anode materials for the lithium-ion batteries have been attracting intensive attentions in recent years due to their high energy capacity and low toxicity. A new Fe3O4/C composite with hollow spheres in porous three-dimensional (3D) nanostructure, which was synthesized by a facile solvothermal method using FeCl3·6H2O and porous spongy carbon as raw materials. The specific surface area and microstructures of composite were characterized by nitrogen adsorption-desorption isotherm method, FE-SEM and HR-TEM. A homogeneous distribution of hollow Fe3O4 spheres (diameter ranges from 120 nm to 150 nm) in the spongy carbon (pore size > 200 nm) conductive 3D-network significantly reduced the lithium-ion diffusion length and increased the electrochemical reaction area, and further more enhanced the lithium ion battery performance, such as discharge capacity and cycle life. As an anode material for the lithium-ion battery, the title composite exhibit excellent electrochemical properties. The Fe3O4/C composite electrode achieved a relatively high reversible specific capacity of 1450.1 mA h g-1 in the first cycle at 100 mA g-1, and excellent rate capability (69% retention at 1000 mA g-1) with good cycle stability (only 10% loss after 100 cycles).

Ion transport studies on Pb(NO3)2:Al2O3 composite solid electrolytes: Effect of dispersoid particle size

Science.gov (United States)

Reddy, Y. Govinda; Sekhar, M. Chandra; Sadananda Chary, A.; Narender Reddy, S.

2018-02-01

Composites of Alumina dispersed Lead Nitrate of different particles sizes (0.3µm, 36.9µm) were prepared through mechanical mixing process. These composites have been characterized by using XRD and SEM. Transport properties of these systems have been studied by means of impedance spectroscopy in the frequency range 100Hz to 4MHz in the temperature range from room temperature to 300°C. Temperature dependent conductivity spectra for composites with different mole percentages of alumina and with different particle sizes (0.3µm, 36.9µm) studied. The contact surface area between host and dispersoid increases with the decrease in particle size. These studies indicate that the conductivity in these systems is mainly due to the contribution enhanced concentration of mobile ions at the interfacial regions of host and dispersoid materials and increased mobility of charge carriers along the grain boundaries. It is believed that mechanism of conductivity through anti-Frenkel disorder (NO3 - ions) in these composites.

Kinetics of the glucose/glycine Maillard reaction pathways: influences of pH and reactant initial concentrations

NARCIS (Netherlands)

Martins, S.I.F.S.; Boekel, van M.A.J.S.

2005-01-01

A previously proposed kinetic model for the glucose/glycine Maillard reaction pathways has been validated by changing the initial pH (4.8, 5.5, 6.0, 6.8 and 7.5) of the reaction and reactant initial concentrations (1:2 and 2:1 molar ratios were compared to the 1:1 ratio). The model consists of 10

N-doped graphene/graphite composite as a conductive agent-free anode material for lithium ion batteries with greatly enhanced electrochemical performance

International Nuclear Information System (INIS)

Guanghui, Wu; Ruiyi, Li; Zaijun, Li; Junkang, Liu; Zhiguo, Gu; Guangli, Wang

2015-01-01

Graphical abstract: The study reported a novel N-doped graphene/graphite anode material for lithium ion batteries. The composite exhibits a largely enhanced electrochemical performance. The study also provides an attractive approach for the fabrication of various graphite-based materials for high power batteries. Display Omitted -- Highlights: • The paper developed a new N-doped graphene/graphite composite for lithium ion battery • The composite contains a three-dimensional graphene framework with rich of open pores • The hybrid offers a higher electrical conductivity when compared with pristine graphite • The hybrid electrode provides a greatly enhanced electrochemical performance • The study provides a prominent approach for fabrication of graphite-based materials -- ABSTRACT: Present graphite anode cannot meet the increasing requirement of electronic devices and electric vehicles due to its low specific capacity, poor cycle stability and low rate capability. The study reported a promising N-doped graphene/graphite composite as a conductive agent-free anode material for lithium ion batteries. Herein, graphite oxide and urea were dispersed in ultrapure water and partly reduced by ascorbic acid. Followed by mixing with graphite and hydrothermal treatment to produce graphene oxide/graphite hydrogel. The hydrogel was dried and finally annealed in Ar/H 2 to obtain N-doped graphene/graphite composite. The result shows that all of graphite particles was dispersed in three-dimensional graphene framework with a rich of open pores. The open pore accelerates the electrolyte transport. The graphene framework works as a conductive agent and graphite particle connector and improves the electron transfer. Electrical conductivity of the composite reaches 5912 S m −1 , which is much better than that of the pristine graphite (4018 S m −1 ). The graphene framework also acts as an expansion absorber in the anodes of lithium ion battery to relieve the large strains

Characterization of silicon- and carbon-based composite anodes for lithium-ion batteries

International Nuclear Information System (INIS)

Khomenko, Volodymyr G.; Barsukov, Viacheslav Z.

2007-01-01

In recent years development of active materials for negative electrodes has been of great interest. Special attention has been focused on the active materials possessing higher reversible capacity than that of conventional graphite. In the present work the electrochemical performance of some carbon/silicon-based materials has been analyzed. For this purpose various silicon-based composites were prepared using such carbon materials as graphite, hard carbon and graphitized carbon black. An analysis of charging-discharging processes at electrodes based on different carbon materials has shown that graphite modified with silicon is the most promising anode material. It has also been revealed that the irreversible capacity mainly depends on the content of Si. An optimum content of Si has been determined with taking into account that high irreversible capacity is not suitable for practical application in lithium-ion batteries. This content falls within the range of 8-10 wt%. The reversible capacity of graphite modified with 8 wt% carbon-coated Si was as high as 604 mAh g -1 . The irreversible capacity loss with this material was as low as 8.1%. The small irreversible capacity of the material allowed developing full lithium-ion rechargeable cells in the 2016 coin cell configuration. Lithium-ion batteries based on graphite modified with silicon show gravimetric and volumetric specific energy densities which are higher by approximately 20% than those for a lithium-ion battery based on natural graphite

In situ Raman spectroscopic studies on concentration change of electrolyte salt in a lithium ion model battery with closely faced graphite composite and LiCoO2 composite electrodes by using an ultrafine microprobe

International Nuclear Information System (INIS)

Yamanaka, Toshiro; Nakagawa, Hiroe; Tsubouchi, Shigetaka; Domi, Yasuhiro; Doi, Takayuki; Abe, Takeshi; Ogumi, Zempachi

2017-01-01

The concentration of ions in the electrolyte solution in lithium ion batteries changes during operation, reflecting the resistance to ion migration and the positions of diffusion barriers. The change causes various negative effects on the performance of batteries. Thus, it is important to elucidate how the concentration changes during operation. In this work, the concentration change of ions in the electrolyte solution in deep narrow spaces in a realistic battery was studied by in situ ultrafine microprobe Raman spectroscopy. Graphite composite and LiCoO 2 composite electrodes, which are the most commonly used electrodes in practical batteries, were placed facing each other and their distance was set to 80 μm, which is close to the distance between electrodes in practical batteries. After repeated charge/discharge cycles, the concentration of ions increased and decreased greatly during charging and discharging, respectively. The maximum concentration was more than three-times higher than the minimum concentration. The rate of changes in concentration increased almost linearly with increase in current density. The results have important implications about concentration changes of ions occurring in practical batteries.

Structural and composition investigations at delayered locations of low k integrated circuit device by gas-assisted focused ion beam

Energy Technology Data Exchange (ETDEWEB)

Wang, Dandan, E-mail: dandan.wang@globalfoundries.com; Kee Tan, Pik; Yamin Huang, Maggie; Lam, Jeffrey; Mai, Zhihong [Technology Development Department, GLOBALFOUNDRIES Singapore Pte. Ltd., 60 Woodlands Industrial Park D, Street 2, Singapore 738406 (Singapore)

2014-05-15

The authors report a new delayering technique – gas-assisted focused ion beam (FIB) method and its effects on the top layer materials of integrated circuit (IC) device. It demonstrates a highly efficient failure analysis with investigations on the precise location. After removing the dielectric layers under the bombardment of an ion beam, the chemical composition of the top layer was altered with the reduced oxygen content. Further energy-dispersive x-ray spectroscopy and Fourier transform infrared analysis revealed that the oxygen reduction lead to appreciable silicon suboxide formation. Our findings with structural and composition alteration of dielectric layer after FIB delayering open up a new insight avenue for the failure analysis in IC devices.

Treatment of low level radioactive liquid wastes using composite ion-exchange resins based on polyurethane foam

International Nuclear Information System (INIS)

Rao, S.V.S.; Lekshmi, R.; Mani, A.G.S.; Sinha, P.K.

2010-01-01

Composite ion-exchange resins were prepared by coating copper-ferrocyanide (CFC) and hydrous manganese oxide (HMO) powders on polyurethane (PU) foam. Polyvinyl acetate/Acetone was used as a binder. The foam was loaded with about five times its weight with CFC and HMO powders. The distribution coefficients of CFC-PU foam and HMO-PU foam for cesium and strontium respectively were estimated. Under similar conditions the HMO-PU foam showed higher capacity as well as better kinetics for removal of strontium than CFC-PU foam for Cs. The pilot plant scale studies were conducted using a mixed composite ion-exchange resin bed. About 1000 bed volumes could be passed before attaining a DF of 10 from an initial value of 60-80. The spent resin was digested in alkaline KMnO 4 and the digested liquid was fixed in cement matrix. The matrices were characterized with respect to compressive strength and leach resistance. (author)

Effect of sulfate ions on the crystallization and photocatalytic activity of TiO2/diatomite composite photocatalyst

Science.gov (United States)

Zhang, Jinjun; Wang, Xiaoyan; Wang, Jimei; Wang, Jing; Ji, Zhijiang

2016-01-01

TiO2 nanoparticles were immobilized on diatomite by hydrolysis-deposition method using titanium tetrachloride as precursor. The effect of sulfate ions on the crystallization and photocatalytic activity of TiO2/diatomite composite photocatalyst was characterized by TG-DSC, XRD, BET surface area, SEM, FT-IR spectroscopy, XPS and UV-vis diffuse reflectance spectra. The results indicate that addition of a small amount of sulfate ions promotes the formation of anatase phase and inhibits the transformation from anatase to rutile. On the other hand, sulfate ions immobilized on the surface of TiO2/diatomite have strong affinity for electrons, capturing the photo-generated electrons, which hinders the recombination of electrons and holes.

Microstructure and wear resistance of Al2O3-M7C3/Fe composite coatings produced by laser controlled reactive synthesis

Science.gov (United States)

Tan, Hui; Luo, Zhen; Li, Yang; Yan, Fuyu; Duan, Rui

2015-05-01

Based on the principle of thermite reaction of Al and Fe2O3 powders, the Al2O3 ceramic reinforced Fe-based composite coatings were fabricated on a steel substrate by laser controlled reactive synthesis and cladding. The effects of different additions of thermite reactants on the phase transition, microstructure evolution, microhardness and wear resistance of the composite coatings were investigated by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Vickers microhardness and block-on-ring wear test, respectively. The results show that Al2O3 ceramic and M7C3 carbide are in situ synthesized via the laser controlled reactive synthesis. The Al2O3 ceramic and M7C3 carbides prefer to distribute along the γ-Fe phase boundary continuously, which separates the γ-Fe matrix and is beneficial to the grain refinement. With the increase of thermite reactants, the amount of Al2O3 ceramic and M7C3 carbide in the composite coatings increases gradually. Moreover the cladding layer changes from dendritic structure to columnar structure and martensite structure in the heat affected zone becomes coarse. The increased thermite reactants improve the microhardness and wear resistance of the in situ composite coatings obviously and enhance the hardness of the heat affected zone, which should be ascribed to the grain refinement, ceramic and carbide precipitation and solid solution strengthening.

Synthesis and electrochemical characteristics of Sn-Sb-Ni alloy composite anode for Li-ion rechargeable batteries

International Nuclear Information System (INIS)

Guo Hong; Zhao Hailei; Jia Xidi; Qiu Weihua; Cui Fenge

2007-01-01

Micro-scaled Sn-Sb-Ni alloy composite was synthesized from oxides of Sn, Sb and Ni via carbothermal reduction. The phase composition and electrochemical properties of the Sn-Sb-Ni alloy composite anode material were studied. The prepared alloy composite electrode exhibits a high specific capacity and a good cycling stability. The lithiation capacity was 530 mAh g -1 in the first cycle and maintained at 370-380 mAh g -1 in the following cycles. The good electrochemical performance may be attributed to its relatively large particle size and multi-phase characteristics. The former reason leads to the lower surface impurity and thus the lower initial capacity loss, while the latter results in a stepwise lithiation/delithiation behavior and a smooth volume change of electrode in cycles. The Sn-Sb-Ni alloy composite material shows a good candidate anode material for the rechargeable lithium ion batteries

Hierarchical carambola-like Li4Ti5O12-TiO2 composites as advanced anode materials for lithium-ion batteries

International Nuclear Information System (INIS)

Zhang, Yu; Zhang, Yun; Huang, Ling; Zhou, Zhongfu; Wang, Jingfeng; Liu, Heng; Wu, Hao

2016-01-01

Hierarchically structured Li 4 Ti 5 O 12 -TiO 2 (LTO-TiO 2 ) composites are synthesized using a facile hydrothermal approach upon reaction time control. With control over the time of hydrothermal reaction at 18 h, a hierarchical dual-phase LTO-TiO 2 composite with appropriate amount of anatase TiO 2 can be obtained, and it possesses a uniform carambola-like framework assembled by numerous ultrathin nanosheets, which enable a relatively large specific surface area, along with abundant interlayer channels to favor electrolyte penetration. When used as anode materials for lithium-ion batteries, such carambola-like LTO-TiO 2 composite exhibits remarkably improved capacity, high-rate capability, and cycling stability over other LTO-TiO 2 samples, which are synthesized at different time of hydrothermal reaction. Specifically, it deliveries a discharge capacity as high as 115.1 and 91.2 mAh g −1 at a very high current rate of 20 and 40C, respectively, while a stable reversible capacity of 171.7 mAh g −1 can be retained after 200 charge-discharge cycles at 1C, corresponding to 88.6% capacity retention. The excellent electrochemical performances benefit from the unique hierarchical carambola-like structure together with the mutually complementary intrinsic advantages between LTO and TiO 2 . The robust and porous nanosheets-assembled LTO-TiO 2 framework not only offers a shorter transport pathway for electron and Li-ion migration within this composite material, but also is able to alleviate the structure distortion during the fast Li-ion insertion/extraction process. The work described here shows that the hierarchical carambola-like LTO-TiO 2 composite is a promising anode material for high-power and long-life lithium-ion batteries.

A mesoporous WO3−X/graphene composite as a high-performance Li-ion battery anode

International Nuclear Information System (INIS)

Liu, Fei; Kim, Jong Gu; Lee, Chul Wee; Im, Ji Sun

2014-01-01

Graphical abstract: The highly flexible and conductive graphene layer can enhance electron transfer, protect metal oxides against disintegration and aggregation and buffer the strain induced by volume expansion during cycles. The mesoporous surface layer provides an open network for Li+ diffusion. - Highlights: • Novel cocktail effects of 2D mesoporous WO 3−X /graphene for lithium ion battery. • New approach for lithium ion battery by easy and unique synthesis method. • Mechanism study with proper data for understanding a reaction on anode surface. - Abstract: A novel mesoporous WO 3−X /graphene composite was developed. This material allowed rapid electron and Li + ion diffusion when used as a Li-ion battery (LIB) anode material. Remarkably, the graphene support protected WO 3−X from changing volume during the electrochemical cycling process; this process generally induces capacity loss. The current work describes a high-performance anode material for LIB that has highly dense WO 3−X , as well as high capacity, rate capability and stability

Recent progress in understanding of the ion composition in the magnetosphere and some major question mark

International Nuclear Information System (INIS)

Hultqvist, B.

1981-06-01

The observations of the energetic ion composition in the magnetosphere are reviewed with the emphasis on the recent measurements by means of GEOS-1 and -2, ISEE-1 and 2, PROGNOZ-7 and SCATHA. The observations are compared with the predictions of the open magnetosphere model. One of the major conclusions is that there are processes in the magnetosphere which play a much larger part than the model, as hitherto presented, predicts. Direct ejection of ionospheric ions, in combination with acceleration, along closed as well as open field lines may even be the dominating source process for the ring current/inner plasma sheet in magnetic storms. In very disturbed conditions this ejection mechanism must work over most of the hemispheres poleward of say 50degrees. Circulation of the ionospheric ions through the tail of the magnetosphere is not likely to be of primary importance for the energization of these ions in very disturbed conditions. (author)

Effects of annealing on the properties of atomic layer deposited Ru thin films deposited by NH{sub 3} and H{sub 2} as reactants

Energy Technology Data Exchange (ETDEWEB)

Lee, Seung-Joon; Kim, Soo-Hyun, E-mail: soohyun@ynu.ac.kr

2016-08-01

Atomic layer deposition (ALD) of Ru using a non-oxidizing reactant is indispensable considering its application as a seed layer for Cu electroplating and a bottom electrode for dynamic random access memory capacitors. In this study, ALD-Ru films were deposited using a sequential supply of dicarbonyl-bis(5-methyl-2,4-hexanediketonato) Ru(II) (C{sub 16}H{sub 22}O{sub 6}Ru) and potential non-oxidizing reducing agents, NH{sub 3} or H{sub 2}, as the reactants at a substrate temperature of 250 °C, and the effects of post-annealing in a H{sub 2} ambient on the film properties were investigated. The highly conformal deposition of Ru films was possible using the present reaction scheme but its resistivity was as high as ~ 750 μΩ-cm due to carbon incorporation into the film and the formation of an amorphous structure. Low temperature annealing at 300 °C at H{sub 2} ambient after deposition was found to improve the properties significantly in terms of the resistivity, impurities contents and crystallinity. For example, the film resistivity was decreased drastically to ~ 40 μΩ-cm with both the release of C in the film and crystallization after annealing based on secondary ion mass spectrometry and transmission electron microscopy, whereas perfect step coverage at a very small-sized dual trench (aspect ratio: ~ 3, the top opening size of 45 nm and bottom size of 20 nm) was maintained after annealing. - Highlights: • Ru thin films were deposited by atomic layer deposition (ALD) using NH{sub 3} and H{sub 2} molecules. • Effects of low temperature (300 °C) post-annealing on the film properties were investigated. • Post annealing improved the properties of ALD-Ru films. • Perfect step coverage of ALD-Ru was confirmed at trench structure (top opening width: 45 nm).

Synthesis and optimization of tin dioxide/functionalized multi-walled carbon nanotube composites as anode in lithium-ion battery

Energy Technology Data Exchange (ETDEWEB)

Xu, Xiao-Bing; Geng, Hong-Zhang, E-mail: genghz@tjpu.edu.cn; Meng, Yan; Ding, Er-Xiong; Wang, Yan; Zhang, Ze-Chen; Wang, Wen-Yi

2015-03-01

In this paper, nanocomposite electrodes for rechargeable Lithium-ion battery composed of tin dioxide (SnO{sub 2}) and multi-walled carbon nanotubes (MWCNTs) were prepared using the chemical deposition method with a subsequent sintering process. The as-prepared hybrids were characterized by thermal gravimetric analysis, Fourier transform infrared spectroscopy, X-ray diffraction and transmission electron microscopy. The results showed that the size of pure SnO{sub 2} particles was ∼5 nm and hybrids presented a uniform dispersion of SnO{sub 2} nanoparticles on the surfaces of the MWCNTs. The electrochemical properties of the composites were researched through a cyclic voltammetry and a galvanostatic charge–discharge test. It was found that the electrochemical performance of the composite was strongly dependent on the content of MWCNTs in the composites. The SnO{sub 2}/MWCNT composite with 18.40 wt% MWCNTs gave the best performance, exhibiting a relatively higher reversible capacity of 475 mAh g{sup −1} and an extended capacity retention of 65% even after 30 cycles at a current density of 78.2 mA g{sup −1}. - Highlights: • SnO{sub 2}/MWCNT nanocomposites were prepared using chemical deposition method. • SnO{sub 2} nanoparticles presented a uniformly dispersion on the surfaces of MWCNTs. • SnO{sub 2}/MWCNT composite anode exhibited high reversible capacity for rechargeable Li-ion battery.

Synthesis and optimization of tin dioxide/functionalized multi-walled carbon nanotube composites as anode in lithium-ion battery

International Nuclear Information System (INIS)

Xu, Xiao-Bing; Geng, Hong-Zhang; Meng, Yan; Ding, Er-Xiong; Wang, Yan; Zhang, Ze-Chen; Wang, Wen-Yi

2015-01-01

In this paper, nanocomposite electrodes for rechargeable Lithium-ion battery composed of tin dioxide (SnO 2 ) and multi-walled carbon nanotubes (MWCNTs) were prepared using the chemical deposition method with a subsequent sintering process. The as-prepared hybrids were characterized by thermal gravimetric analysis, Fourier transform infrared spectroscopy, X-ray diffraction and transmission electron microscopy. The results showed that the size of pure SnO 2 particles was ∼5 nm and hybrids presented a uniform dispersion of SnO 2 nanoparticles on the surfaces of the MWCNTs. The electrochemical properties of the composites were researched through a cyclic voltammetry and a galvanostatic charge–discharge test. It was found that the electrochemical performance of the composite was strongly dependent on the content of MWCNTs in the composites. The SnO 2 /MWCNT composite with 18.40 wt% MWCNTs gave the best performance, exhibiting a relatively higher reversible capacity of 475 mAh g −1 and an extended capacity retention of 65% even after 30 cycles at a current density of 78.2 mA g −1 . - Highlights: • SnO 2 /MWCNT nanocomposites were prepared using chemical deposition method. • SnO 2 nanoparticles presented a uniformly dispersion on the surfaces of MWCNTs. • SnO 2 /MWCNT composite anode exhibited high reversible capacity for rechargeable Li-ion battery

Mechanical properties and ion release from bioactive restorative composites containing glass fillers and calcium phosphate nano-structured particles.

Science.gov (United States)

Chiari, Marina D S; Rodrigues, Marcela C; Xavier, Tathy A; de Souza, Eugen M N; Arana-Chavez, Victor E; Braga, Roberto R

2015-06-01

To evaluate the effect of the replacement of barium glass by dicalcium phosphate dihydrate (DCPD) particles on the mechanical properties and degree of conversion (DC) of composites. Additionally, calcium and hydrogen phosphate (HPO4(2-)) release were followed for 28 days. Nine composites containing equal parts (in mols) of BisGMA and TEGDMA and 40, 50 or 60 vol% of total filler were manipulated. Filler phase was constituted by silanated barium glass and 0%, 10% or 20% of DCPD particles. DC was determined by near-FTIR. Biaxial flexural strength (BFS) and modulus (E) were tested using the "piston on three balls" method, while fracture toughness (KIc) used the "single edge notched beam" method. Specimens were tested after 24h and 28 days in water. Ion release was determined using inductively coupled plasma optical emission spectrometry (ICP-OES). Data were analyzed by ANOVA/Tukey (DC and ion release) or Kruskal-Wallis/Mann-Whitney (mechanical properties; alpha: 5%). DC was not affected by DCPD. The presence of DCPD reduced BFS for both storage times, while differences in E became evident after 28 days. After 24h, KIc increased with the addition of DCPD; after 28 days, however, KIc decreased only for DCPD-containing composites. Calcium release was similar for both DCPD contents and remained fairly constant during the 28-day period. Overall, HPO4(2-) release was higher at 7 days and did not decrease after 14 days. The composite with the highest filler level and 10% DCPD represented the best compromise between mechanical properties after aging in water and ion release. Copyright © 2015 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

Fabrication and Characterization of SnO2/Graphene Composites as High Capacity Anodes for Li-Ion Batteries

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Abirami Dhanabalan

2013-11-01

Full Text Available Tin-oxide and graphene (TG composites were fabricated using the Electrostatic Spray Deposition (ESD technique, and tested as anode materials for Li-ion batteries. The electrochemical performance of the as-deposited TG composites were compared to heat-treated TG composites along with pure tin-oxide films. The heat-treated composites exhibited superior specific capacity and energy density than both the as-deposited TG composites and tin oxide samples. At the 70th cycle, the specific capacities of the as-deposited and post heat-treated samples were 534 and 737 mA·h/g, respectively, and the corresponding energy densities of the as-deposited and heat-treated composites were 1240 and 1760 W·h/kg, respectively. This improvement in the electrochemical performance of the TG composite anodes as compared to the pure tin oxide samples is attributed to the synergy between tin oxide and graphene, which increases the electrical conductivity of tin oxide and helps alleviate volumetric changes in tin-oxide during cycling.

Nanoporous titanium niobium oxide and titanium tantalum oxide compositions and their use in anodes of lithium ion batteries

Science.gov (United States)

Dai, Sheng; Guo, Bingkun; Sun, Xiao-Guang; Qiao, Zhenan

2017-10-31

Nanoporous metal oxide framework compositions useful as anodic materials in a lithium ion battery, the composition comprising metal oxide nanocrystals interconnected in a nanoporous framework and having interconnected channels, wherein the metal in said metal oxide comprises titanium and at least one metal selected from niobium and tantalum, e.g., TiNb.sub.2-x Ta.sub.xO.sub.y (wherein x is a value from 0 to 2, and y is a value from 7 to 10) and Ti.sub.2Nb.sub.10-vTa.sub.vO.sub.w (wherein v is a value from 0 to 2, and w is a value from 27 to 29). A novel sol gel method is also described in which sol gel reactive precursors are combined with a templating agent under sol gel reaction conditions to produce a hybrid precursor, and the precursor calcined to form the anodic composition. The invention is also directed to lithium ion batteries in which the nanoporous framework material is incorporated in an anode of the battery.

Solvent transfer of graphene oxide for synthesis of tin mono-sulfide graphene composite and application as anode of lithium-ion battery

Energy Technology Data Exchange (ETDEWEB)

Tripathi, Alok M., E-mail: alokmani@iitb.ac.in; Mitra, Sagar

2016-11-15

Graphical abstract: Destabilization of graphene oxide colloid and SnS graphene composite preparation for lithium-ion battery. - Abstract: Tin mono sulfide (SnS) graphene composite has been synthesized for anode of lithium-ion battery. For synthesis of composite, graphene oxide (GO)-water (H{sub 2}O) colloid has been destabilized and ensured the complete transfer of graphene oxide into another organic solvent N, N-dimethyl formamide (DMF). Mechanism for the destabilization of GO-H{sub 2}O colloid is established. Surface to surface attachment of SnS on graphene sheet is achieved by solvothermal solution phase assembly of graphene sheets and SnS nanoparticles in DMF solvent. Graphene plays role in nanoparticle formation in composite. Such confined composite has been cycled reversibly at current rate of 160 mA g{sup −1}, in voltage region of 0.01–2.5 V and exhibit a superior discharge capacity of 630 mAh g{sup −1} after 50th cycle. Ex situ TEM analysis of used electrode reveal that the SnS nanoparticle-graphene composite with CMC binder perform better due to proper shape retention of electroactive materials during electrochemical cycling.

Solvent transfer of graphene oxide for synthesis of tin mono-sulfide graphene composite and application as anode of lithium-ion battery

International Nuclear Information System (INIS)

Tripathi, Alok M.; Mitra, Sagar

2016-01-01

Graphical abstract: Destabilization of graphene oxide colloid and SnS graphene composite preparation for lithium-ion battery. - Abstract: Tin mono sulfide (SnS) graphene composite has been synthesized for anode of lithium-ion battery. For synthesis of composite, graphene oxide (GO)-water (H_2O) colloid has been destabilized and ensured the complete transfer of graphene oxide into another organic solvent N, N-dimethyl formamide (DMF). Mechanism for the destabilization of GO-H_2O colloid is established. Surface to surface attachment of SnS on graphene sheet is achieved by solvothermal solution phase assembly of graphene sheets and SnS nanoparticles in DMF solvent. Graphene plays role in nanoparticle formation in composite. Such confined composite has been cycled reversibly at current rate of 160 mA g"−"1, in voltage region of 0.01–2.5 V and exhibit a superior discharge capacity of 630 mAh g"−"1 after 50th cycle. Ex situ TEM analysis of used electrode reveal that the SnS nanoparticle-graphene composite with CMC binder perform better due to proper shape retention of electroactive materials during electrochemical cycling.

One-Pot Synthesis of CoSex -rGO Composite Powders by Spray Pyrolysis and Their Application as Anode Material for Sodium-Ion Batteries.

Science.gov (United States)

Park, Gi Dae; Kang, Yun Chan

2016-03-14

A simple one-pot synthesis of metal selenide/reduced graphene oxide (rGO) composite powders for application as anode materials in sodium-ion batteries was developed. The detailed mechanism of formation of the CoSe(x)-rGO composite powders that were selected as the first target material in the spray pyrolysis process was studied. The crumple-structured CoSe(x)-rGO composite powders prepared by spray pyrolysis at 800 °C had a crystal structure consisting mainly of Co0.85 Se with a minor phase of CoSe2. The bare CoSe(x) powders prepared for comparison had a spherical shape and hollow structure. The discharge capacities of the CoSe(x)-rGO composite and bare CoSe(x) powders in the 50th cycle at a constant current density of 0.3 A g(-1) were 420 and 215 mA h g(-1), respectively, and their capacity retentions measured from the second cycle were 80 and 46%, respectively. The high structural stability of the CoSe(x)-rGO composite powders for repeated sodium-ion charge and discharge processes resulted in superior sodium-ion storage properties compared to those of the bare CoSe(x) powders. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Hierarchical shell/core CuO nanowire/carbon fiber composites as binder-free anodes for lithium-ion batteries

International Nuclear Information System (INIS)

Yuan, Wei; Luo, Jian; Pan, Baoyou; Qiu, Zhiqiang; Huang, Shimin; Tang, Yong

2017-01-01

Highlights: •The composite anode is composed of CuO nanowire shell and carbon fiber core. •The composite anode avoids completely the use of binders. •Synergistic effect of carbon fibers and CuO nanowires enhances performance. •Carbon fibers improve electrical conductivity and buffer volume change. •CuO nanowires shorten diffusion length and alleviate structural strain. -- Abstract: Developing high-performance electrode structures is of great importance for advanced lithium-ion batteries. This study reports an efficient method to fabricate hierarchical shell/core CuO nanowire/carbon fiber composites via electroless plating and thermal oxidation processes. With this method, a binder-free CuO nanowire/carbon fiber shell/core hierarchical network composite anode for lithium-ion batteries is successfully fabricated. The morphology and chemical composition of the anode are characterized, and the electrochemical performance of the anode is investigated by standard electrochemical tests. Owing to the superior properties of carbon fibers and the morphological advantages of CuO nanowires, this composite anode still retains an excellent reversible capacity of 598.2 mAh g −1 with a capacity retention rate above 86%, even after 50 cycles, which is much higher than the CuO anode without carbon fibers. Compared to the typical CuO/C electrode systems, the novel binder-free anode yields a performance close to that of the typical core/shell electrode systems and a much higher reversible capacity and capacity retention than the similar shell/core patterns as well as the anodes with binders. It is believed that this novel anode will pave the way to the development of binder-free anodes in response to the increasing demands for high-power energy storage.

An excellent performance anode of ZnFe2O4/flake graphite composite for lithium ion battery

International Nuclear Information System (INIS)

Yao, Lingmin; Hou, Xianhua; Hu, Shejun; Tang, Xiaoqin; Liu, Xiang; Ru, Qiang

2014-01-01

Highlights: • ZnFe 2 O 4 /flake graphite composite was synthesized by hydrothermal method. • The ZnFe 2 O 4 /flake graphite anode demonstrated high initial coulombic efficiency of 87.7%. • The initial discharge /charge capacity was 848 mA h g −1 and 744 mA h g −1 . • The high capacity retention of 98% was obtained for the ZnFe 2 O 4 /flake graphite anode. -- Abstract: An approach of hydrothermal reaction for lithium ion battery was adopted, by which ZnFe 2 O 4 /flake graphite composites with excellent performance could be prepared as anode materials for lithium ion batteries. With nano-sized ZnFe 2 O 4 particles coating on the electrochemical active matrix of flake graphite, the special composites allowed improved electronic conductivity and constructed an expressway for the transport of charges and lithium ions. Thus the ZnFe 2 O 4 /flake graphite anode became a compromise between capacity and cycle ability. The initial discharge–charge capacity was 848 mA h g −1 and 744 mA h g −1 at a constant current density of 100 mA g −1 , respectively. As high as 87.7% of the initial coulombic efficiency was obtained. Additionally, the charge capacity maintained constantly in the range of 720–735 mA h g −1 in following cycles. And a high reversible charge capacity of 730 mA h g −1 could be attained after 100 cycles, with the reversible capacity retention of 98%

Photochemical Study of Silver Nanoparticles Formed from the Reduction of Silver Ions by Humic Acid

Science.gov (United States)

Leslie, Renee M.

This study focuses on the ability of silver ions and humic acid to form silver nanoparticles in the presence of UV and visible light. Silver nanoparticles have a number of industrial applications due primarily to their antimicrobial properties, but these properties pose an environmental threat. Silver nanoparticles can directly disrupt sensitive ecosystems by harming bacteria. Consumption of silver nanoparticles results in silver ions and silver nanoparticles entering waterways; the presence of silver ions raises the question of whether nanoparticles can reform in environmental waters. As our data show, silver nanoparticles can form from the reduction of silver ions by humic acid after irradiation with UV and visible light. In order to better understand the mechanism of these naturally synthesized silver nanoparticles, we investigated the effects of reactant concentration, experimental conditions and presence of ions/reactive species. We monitored silver nanoparticle growth with UV-visible spectroscopy. The evolution in time of nanoparticle size was monitored by dynamic light scattering (DLS).

MnO{sub 2} nanorods/3D-rGO composite as high performance anode materials for Li-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Liu, Hongdong; Hu, Zhongli; Su, Yongyao; Ruan, Haibo; Hu, Rong [Research Institute for New Materials Technology, Chongqing University of Arts and Sciences, Chongqing 402160 (China); Zhang, Lei, E-mail: leizhang0215@126.com [College of Life Science, Chongqing Normal University, Chongqing 401331 (China)

2017-01-15

Highlights: • MnO{sub 2} nanorods/3D-rGO composite has been synthesized by a simple in situ hydrothermal methord. • MnO{sub 2} nanorods/3D-rGO composite exhibits high reversible capacity, outstanding rate capacity and excellent cyclic stability. • Building metal oxides/3D-rGO composite is an effective way for improving the electrochemical performance of Li-ion batteries. - Abstract: MnO{sub 2} nanorods/three-dimensional reduced graphene oxide (3D-rGO) composite has been synthesized by a simple in situ hydrothermal methord. The X-ray diffraction (XRD) pattern of the as-prepared composite reveals tetragonal structure of α-MnO{sub 2.} Raman spectroscopic and X-ray photoelectron spectroscopy (XPS) of the samples confirm the coexistence of MnO{sub 2} and graphene. The Brunauer-Emmett-Teller (BET) analysis shows the large surface area of the composite. The electron microscopy images of the as-synthesized products reveals the MnO{sub 2} nanorods are homogeneously grown on 3D-rGO matrix. Electrochemical characterization exhibits the MnO{sub 2} nanorods/3D-rGO composite with large reversible capacity (595 mA h g{sup −1} over 60 cycles at 100 mA g{sup −1}), high coulombic efficiency (above 99%), excellent rate capability and good cyclic stability. The superior electrochemical performance can be attributed to the turf-like nanostructure of composite, high capacity of MnO{sub 2} and superior electrical conductivity of 3D-rGO. It suggests that MnO{sub 2} nanorods/3D-rGO composite will be a promising anode material for Li-ion batteries.

Efficient reduced graphene oxide grafted porous Fe3O4 composite as a high performance anode material for Li-ion batteries.

Science.gov (United States)

Bhuvaneswari, Subramani; Pratheeksha, Parakandy Muzhikara; Anandan, Srinivasan; Rangappa, Dinesh; Gopalan, Raghavan; Rao, Tata Narasinga

2014-03-21

Here, we report facile fabrication of Fe3O4-reduced graphene oxide (Fe3O4-RGO) composite by a novel approach, i.e., microwave assisted combustion synthesis of porous Fe3O4 particles followed by decoration of Fe3O4 by RGO. The characterization studies of Fe3O4-RGO composite demonstrate formation of face centered cubic hexagonal crystalline Fe3O4, and homogeneous grafting of Fe3O4 particles by RGO. The nitrogen adsorption-desorption isotherm shows presence of a porous structure with a surface area and a pore volume of 81.67 m(2) g(-1), and 0.106 cm(3) g(-1) respectively. Raman spectroscopic studies of Fe3O4-RGO composite confirm the existence of graphitic carbon. Electrochemical studies reveal that the composite exhibits high reversible Li-ion storage capacity with enhanced cycle life and high coulombic efficiency. The Fe3O4-RGO composite showed a reversible capacity ∼612, 543, and ∼446 mA h g(-1) at current rates of 1 C, 3 C and 5 C, respectively, with a coulombic efficiency of 98% after 50 cycles, which is higher than graphite, and Fe3O4-carbon composite. The cyclic voltammetry experiment reveals the irreversible and reversible Li-ion storage in Fe3O4-RGO composite during the starting and subsequent cycles. The results emphasize the importance of our strategy which exhibited promising electrochemical performance in terms of high capacity retention and good cycling stability. The synergistic properties, (i) improved ionic diffusion by porous Fe3O4 particles with a high surface area and pore volume, and (ii) increased electronic conductivity by RGO grafting attributed to the excellent electrochemical performance of Fe3O4, which make this material attractive to use as anode materials for lithium ion storage.

Facile synthesis of hierarchical nanostructured rutile titania for lithium-ion battery

International Nuclear Information System (INIS)

Fei Hailong; Wei Mingdeng

2011-01-01

Highlights: → Rutile TiO 2 sub-microflowers and sub-microspheres with different building blocks as anode materials of lithium-ion battery. → Controllable morphologies with oxalic acid by the hydrothermal technique. → Sub-microflower and sub-microspheres constructed by well organized nanorods exhibited high capacity and good cycle stability. → Small size building blocks nanorods enhance the transfer rate of Li-ion. - Abstract: A facile hydrothermal method is developed to prepare rutile titania sub-microflowers consisting of nanorods with oxalic acid and TiOSO 4 as reagents. The diameter of sub-microflowers and nanorods is found to be ca. 800 and 40 nm, respectively. Also, the shape and size of building blocks in rutile titania sub-microflowers can be considerably controlled via adjusting the reaction time and reactant amounts. Rutile titania sub-microflowers composed of nanorods display higher discharge capacity and better rate cycle stability than other rutile titania nanostructures as lithium-ion battery anode material due to enhancing the Li-ion transfer rate for small size building blocks.

Advanced carbon materials/olivine LiFePO4 composites cathode for lithium ion batteries

Science.gov (United States)

Gong, Chunli; Xue, Zhigang; Wen, Sheng; Ye, Yunsheng; Xie, Xiaolin

2016-06-01

In the past two decades, LiFePO4 has undoubtly become a competitive candidate for the cathode material of the next-generation LIBs due to its abundant resources, low toxicity and excellent thermal stability, etc. However, the poor electronic conductivity as well as low lithium ion diffusion rate are the two major drawbacks for the commercial applications of LiFePO4 especially in the power energy field. The introduction of highly graphitized advanced carbon materials, which also possess high electronic conductivity, superior specific surface area and excellent structural stability, into LiFePO4 offers a better way to resolve the issue of limited rate performance caused by the two obstacles when compared with traditional carbon materials. In this review, we focus on advanced carbon materials such as one-dimensional (1D) carbon (carbon nanotubes and carbon fibers), two-dimensional (2D) carbon (graphene, graphene oxide and reduced graphene oxide) and three-dimensional (3D) carbon (carbon nanotubes array and 3D graphene skeleton), modified LiFePO4 for high power lithium ion batteries. The preparation strategies, structure, and electrochemical performance of advanced carbon/LiFePO4 composite are summarized and discussed in detail. The problems encountered in its application and the future development of this composite are also discussed.

Self-assembly silicon/porous reduced graphene oxide composite film as a binder-free and flexible anode for lithium-ion batteries

International Nuclear Information System (INIS)

Tang, H.; Zhang, Y.J.; Xiong, Q.Q.; Cheng, J.D.; Zhang, Q.; Wang, X.L.; Gu, C.D.; Tu, J.P.

2015-01-01

A Si/porous reduced graphene oxide (rGO) composite film synthesized by evaporation and leavening method are developed as a high-performance anode material for lithium ion batteries. The porous structure as buffer base can effectively release the volume expansion of the silicon particles, increase the electrical conductivity and reduce the transfer resistance of Li ions. The Si/porous rGO composite film presents high specific capacity and good cycling stability (1261 mA h g −1 at 50 mA g −1 up to 70 cycles), as well as enhanced rate capability. This approach to prepare such a unique structure is a low-cost and facile route for the silicon-based anode materials

Freestanding rGO-SWNT-STN Composite Film as an Anode for Li Ion Batteries with High Energy and Power Densities

Directory of Open Access Journals (Sweden)

Taeseup Song

2015-12-01

Full Text Available Freestanding Si-Ti-Ni alloy particles/reduced graphene oxide/single wall carbon nanotube composites have been prepared as an anode for lithium ion batteries via a simple filtration method. This composite electrode showed a 9% increase in reversible capacity, a two-fold higher cycle retention at 50 cycles and a two-fold higher rate capability at 2 C compared to pristine Si-Ti-Ni (STN alloy electrodes. These improvements were attributed to the suppression of the pulverization of the STN active material by the excellent mechanical properties of the reduced graphene oxide-single wall carbon nanotube networks and the enhanced kinetics associated with both electron and Li ion transport.

Computational Modelling of Thermal Stability in a Reactive Slab with Reactant Consumption

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O. D. Makinde

2012-01-01

Full Text Available This paper investigates both the transient and the steady state of a one-step nth-order oxidation exothermic reaction in a slab of combustible material with an insulated lower surface and an isothermal upper surface, taking into consideration reactant consumption. The nonlinear partial differential equation governing the transient reaction-diffusion problem is solved numerically using a semidiscretization finite difference technique. The steady-state problem is solved using a perturbation technique together with a special type of the Hermite-Padé approximants. Graphical results are presented and discussed quantitatively with respect to various embedded parameters controlling the systems. The crucial roles played by the boundary conditions in determining the thermal ignition criticality are demonstrated.

Modification of composite por -Si/SnOx power ion beam of nanosecond duration

International Nuclear Information System (INIS)

Korusenko, P.M.; Bolotov, V.V.; Knyazev, E.V.; Kovivchak, V.S.; Korepanov, A.A.; Nesov, S.N.; Povoroznyuk, S.N.

2011-01-01

The results of XPS (X-ray photoelectron spectroscopy), AES (Auger electron spectroscopy) and SEM (Scanning electron microscopy) investigation of tin oxide nanolayers on the samples of the composite por-Si/SnO x with different porosity of the matrix, formed under the influence of a powerful ion beam of nanosecond duration was presented. It is shown that fast melting and crystallization of the surface leads to the formation of globular structures with a typical size of 200 nm. Established that the tin is included in structure of the nanocomposite in the oxidized state with little inclusion of metallic β-tin. With increasing porosity, phase composition of nanolayers of tin is close to the state corresponding to the higher tin oxide SnO 2 . Also shows that with increasing porosity, the intensity of subvalent 4d lines of tin, which is apparently associated with an increased degree of hybridization of the tin atoms and oxygen atoms. According to the results stratified etching was to evaluate the changes of the elemental structure of the composite and the depth of penetration of tin. (authors)

A three-dimensional LiFePO4/carbon nanotubes/graphene composite as a cathode material for lithium-ion batteries with superior high-rate performance

International Nuclear Information System (INIS)

Lei, Xingling; Zhang, Haiyan; Chen, Yiming; Wang, Wenguang; Ye, Yipeng; Zheng, Chuchun; Deng, Peng; Shi, Zhicong

2015-01-01

Graphical abstract: The excellent electrochemical performances can be attributed to the synergistic effect of CNTs and graphene. - Highlights: • The LFP–CNT–G composite was successfully prepared by solid station method. • The interlaced CNTs reduced the crumple of graphene and improved tap density of the composite. • The LFP–CNT–G electrode exhibited superior electrochemical performance. - Abstract: A three-dimensional lithium iron phosphate (LiFePO 4 )/carbon nanotubes (CNTs)/graphene composite was successfully synthesized via solid-state reaction. The LiFePO 4 /carbon nanotubes/graphene (LFP–CNT–G) composite used as Li-ions battery cathode material exhibits superior high-rate capability and favorable charge–discharge cycle performance under relative high current density compared with that of LiFePO 4 /carbon nanotubes (LFP–CNT) composite and LiFePO 4 /graphene (LFP–G) composite. Graphene nanosheets and CNTs construct 3D conducting networks are favor for faster electron transfer, higher Li-ions diffusion coefficient and lower resistance during the Li-ions reversible reaction. The synergistic effect of graphene nanosheets and CNTs improves the rate capability and cycling stability of LiFePO 4 -based cathodes. The LFP–CNT–G electrode shows reversible capacity of 168.9 mA h g −1 at 0.2 C and 115.8 mA h g −1 at 20 C. The electrochemical impedance spectroscopy demonstrate that the LFP–CNT–G electrode has the smallest charge-transfer resistance, indicating that the fast electron transfer from the electrolyte to the LFP–CNT–G active materials in the Li-ions intercalation/deintercalation reactions owing to the three-dimensional networks of graphene and carbon nanotubes

Production of ZrC Matrix for Use in Gas Fast Reactor Composite Fuels

International Nuclear Information System (INIS)

Vasudevamurthy, Gokul; Knight, Travis W.; Roberts, Elwyn; Adams, Thad

2007-01-01

Zirconium carbide is being considered as a candidate for inert matrix material in composite nuclear fuel for Gas fast reactors due to its favorable characteristics. ZrC can be produced by the direct reaction of pure zirconium and graphite powders. Such a reaction is exothermic in nature. The reaction is self sustaining once initial ignition has been achieved. The heat released during the reaction is high enough to complete the reaction and achieve partial sintering without any external pressure applied. External heat source is required to achieve ignition of the reactants and maintain the temperature close to the adiabatic temperature to achieve higher levels of sintering. External pressure is also a driving force for sintering. In the experiments described, cylindrical compacts of ZrC were produced by direct combustion reaction. External induction heating combined with varying amounts of external applied pressure was employed to achieve varying degrees of density/porosity. The effect of reactant particle size on the product characteristics was also studied. The samples were characterized for density/porosity, composition and microstructure. (authors)

Solid-solution-like ZnO/C composites as excellent anode materials for lithium ion batteries

International Nuclear Information System (INIS)

Zhang, Guanhua; Zhang, Hang; Zhang, Xiang; Zeng, Wei; Su, Qingmei; Du, Gaohui; Duan, Huigao

2015-01-01

Exploring advanced anode materials to maximize the capacity of lithium ion batteries has been an active research area for decades. Constructing composites materials has been proved to be one of the most effective methods to achieve higher capacity due to the synergistic effect. In this work, we proposed and demonstrated a concept of solid-solution-like ZnO/C composites to approach the largest possible synergistic effect by introducing the most interfaces and minimizing the pulverization. The solid-solution-like ZnO/C electrode could achieve a high reversible capacity of 813.3 mAh g −1 at a current density of 100 mA g −1 after 100 cycles with a decrease rate of only 0.4% per cycle. Moreover, the discharge capacity still maintained 53.5% of the original value even when the current density increased to 40 times as much as the original, showing a distinguished rate performance. In addition, such solid-solution-like nanofibers can be easily prepared because of their compatibility with the existing industrial PAN-based spinning process. This may pave the way to mass produce lithium ion batteries with significantly enhanced performance using existing low-cost commercial facilities and recipes.

Oxide-Based Composite Electrolytes Using Na3Zr2Si2PO12/Na3PS4 Interfacial Ion Transfer.

Science.gov (United States)

Noi, Kousuke; Nagata, Yuka; Hakari, Takashi; Suzuki, Kenji; Yubuchi, So; Ito, Yusuke; Sakuda, Atsushi; Hayashi, Akitoshi; Tatsumisago, Masahiro

2018-05-31

All-solid-state sodium batteries using Na 3 Zr 2 Si 2 PO 12 (NASICON) solid electrolytes are promising candidates for safe and low-cost advanced rechargeable battery systems. Although NASICON electrolytes have intrinsically high sodium-ion conductivities, their high sintering temperatures interfere with the immediate development of high-performance batteries. In this work, sintering-free NASICON-based composites with Na 3 PS 4 (NPS) glass ceramics were prepared to combine the high grain-bulk conductivity of NASICON and the interfacial formation ability of NPS. Before the composite preparation, the NASICON/NPS interfacial resistance was investigated by modeling the interface between the NASICON sintered ceramic and the NPS glass thin film. The interfacial ion-transfer resistance was very small above room temperature; the area-specific resistances at 25 and 100 °C were 15.8 and 0.40 Ω cm 2 , respectively. On the basis of this smooth ion transfer, NASICON-rich (70-90 wt %) NASICON-NPS composite powders were prepared by ball-milling fine powders of each component. The composite powders were well-densified by pressing at room temperature. Scanning electron microscopy observation showed highly dispersed sub-micrometer NASICON grains in a dense NPS matrix to form closed interfaces between the oxide and sulfide solid electrolytes. The composite green (unfired) compacts with 70 and 80 wt % NASICON exhibited high total conductivities at 100 °C of 1.1 × 10 -3 and 6.8 × 10 -4 S cm -1 , respectively. An all-solid-state Na 15 Sn 4 /TiS 2 cell was constructed using the 70 wt % NASICON composite electrolyte by the uniaxial pressing of the powder materials, and its discharge properties were evaluated at 100 °C. The cell showed the reversible capacities of about 120 mAh g -1 under the current density of 640 μA cm -2 . The prepared oxide-based composite electrolytes were thus successfully applied in all-solid-state sodium rechargeable batteries without sintering.

Column Adsorption Studies for the Removal of Cr(VI Ions by Ethylamine Modified Chitosan Carbonized Rice Husk Composite Beads with Modelling and Optimization

Directory of Open Access Journals (Sweden)

S. Sugashini

2013-01-01

Full Text Available The objective of this present study is the optimization of process parameters in adsorption of Cr(VI ions by ethylamine modified chitosan carbonized rice husk composite beads (EAM-CCRCBs using response surface methodology (RSM and continuous adsorption studies of Cr(VI ions by ethylamine modified chitosan carbonized rice husk composite beads (EAM-CCRCBs. The effect of process variables such as initial metal ion concentration, adsorbent dosage and pH were optimized using RSM in order to ensure high adsorption capacity at low adsorbent dosage and high initial metal ion concentration of Cr(VI in batch process. The optimum condition suggested by the model for the process variable such as adsorbent dosage, pH and initial metal ion concentration was 0.14 g, 300 mg/L and pH2 with maximum removal of 99.8% and adsorption capacity of 52.7 mg/g respectively. Continuous adsorption studies were conducted under optimized initial metal ion concentration and pH for the removal of Cr(VI ions using EAM-CCRCBs. The breakthrough curve analysis was determined using the experimental data obtained from the continuous adsorption. Continuous adsorption modelling such as bed depth service model and Thomson model were established by fitting it with experimental data.

Electron capture in very low energy collisions of multicharged ions with H and D in merged beams

International Nuclear Information System (INIS)

Havener, C.C.; Meyer, F.W.; Phaneuf, R.A.

1991-01-01

An ion-atom merged-beams technique is being used to measure total absolute electron-capture cross sections for multicharged ions in collisions with H (or D) in the energy range between 0.1 and 1000 eV/amu. Comparison between experiment and theory over such a large energy range constitutes a critical test for both experiment and theory. Total capture cross-section measurements for O 3+ H(D) and O 5+ + H(D) are presented and compared to state selective and differential cross section calculations. Landau-Zener calculations show that for O 5+ the sharp increase in the measured cross section below 1 eV/amu is partly due to trajectory effects arising from the ion-induced dipole interaction between the reactants. 20 refs., 8 figs

Ion-Selective Ionic Polymer Metal Composite (IPMC) actuator based on crown ether containing sulfonated Poly(Arylene Ether Ketone)

NARCIS (Netherlands)

Tas, S.; Zoetebier, B.; Sukas, O.S.; Bayraktar, M.; Hempenius, M.; Vancso, G.J.; Nijmeijer, K.

2017-01-01

This study introduces the concept of ion selective actuation in polymer metal composite actuators, employing crown ether bearing aromatic polyether materials. For this purpose, sulfonated poly(arylene ether ketone) (SPAEK) and crown ether containing SPAEK with molar masses suitable for membrane

Graphene nanoribbon and nanostructured SnO2 composite anodes for lithium ion batteries.

Science.gov (United States)

Lin, Jian; Peng, Zhiwei; Xiang, Changsheng; Ruan, Gedeng; Yan, Zheng; Natelson, Douglas; Tour, James M

2013-07-23

A composite made from graphene nanoribbons (GNRs) and tin oxide (SnO2) nanoparticles (NPs) is synthesized and used as the anode material for lithium ion batteries (LIBs). The conductive GNRs, prepared using sodium/potassium unzipping of multiwall carbon nanotubes, can boost the lithium storage performance of SnO2 NPs. The composite, as an anode material for LIBs, exhibits reversible capacities of over 1520 and 1130 mAh/g for the first discharge and charge, respectively, which is more than the theoretical capacity of SnO2. The reversible capacity retains ~825 mAh/g at a current density of 100 mA/g with a Coulombic efficiency of 98% after 50 cycles. Further, the composite shows good power performance with a reversible capacity of ~580 mAh/g at the current density of 2 A/g. The high capacity, good power performance and retention can be attributed to uniformly distributed SnO2 NPs along the high-aspect-ratio GNRs. The GNRs act as conductive additives that buffer the volume changes of SnO2 during cycling. This work provides a starting point for exploring the composites made from GNRs and other transition metal oxides for lithium storage applications.

Detection of nitro-based and peroxide-based explosives by fast polarity-switchable ion mobility spectrometer with ion focusing in vicinity of Faraday detector.

Science.gov (United States)

Zhou, Qinghua; Peng, Liying; Jiang, Dandan; Wang, Xin; Wang, Haiyan; Li, Haiyang

2015-05-29

Ion mobility spectrometer (IMS) has been widely deployed for on-site detection of explosives. The common nitro-based explosives are usually detected by negative IMS while the emerging peroxide-based explosives are better detected by positive IMS. In this study, a fast polarity-switchable IMS was constructed to detect these two explosive species in a single measurement. As the large traditional Faraday detector would cause a trailing reactant ion peak (RIP), a Faraday detector with ion focusing in vicinity was developed by reducing the detector radius to 3.3 mm and increasing the voltage difference between aperture grid and its front guard ring to 591 V, which could remove trailing peaks from RIP without loss of signal intensity. This fast polarity-switchable IMS with ion focusing in vicinity of Faraday detector was employed to detect a mixture of 10 ng 2,4,6-trinitrotoluene (TNT) and 50 ng hexamethylene triperoxide diamine (HMTD) by polarity-switching, and the result suggested that [TNT-H](-) and [HMTD+H](+) could be detected in a single measurement. Furthermore, the removal of trailing peaks from RIP by the Faraday detector with ion focusing in vicinity also promised the accurate identification of KClO4, KNO3 and S in common inorganic explosives, whose product ion peaks were fairly adjacent to RIP.

Compositions and methods of making and using metal-organic framework compositions

KAUST Repository

Mohideen, Mohamed Infas Haja; Adil, Karim; Belmabkhout, Youssef; Eddaoudi, Mohamed; Bhatt, Prashant M.

2017-01-01

Embodiments of the present disclosure include a metal-organic framework (MOF) composition comprising one or more metal ions, a plurality of organic ligands, and a solvent, wherein the one or more metal ions associate with the plurality of organic ligands sufficient to form a MOF with kag topology. Embodiments of the present disclosure further include a method of making a MOF composition comprising contacting one or more metal ions with a plurality of organic ligands in the presence of a solvent, sufficient to form a MOF with kag topology, wherein the solvent comprises water only. Embodiments of the present disclosure also describe a method of capturing chemical species from a fluid composition comprising contacting a MOF composition with kag topology and pore size of about 3.4Å to 4.8Å with a fluid composition comprising two or more chemical species and capturing one or more captured chemical species from the fluid composition.

Compositions and methods of making and using metal-organic framework compositions

KAUST Repository

Mohideen, Mohamed Infas Haja

2017-05-04

Embodiments of the present disclosure include a metal-organic framework (MOF) composition comprising one or more metal ions, a plurality of organic ligands, and a solvent, wherein the one or more metal ions associate with the plurality of organic ligands sufficient to form a MOF with kag topology. Embodiments of the present disclosure further include a method of making a MOF composition comprising contacting one or more metal ions with a plurality of organic ligands in the presence of a solvent, sufficient to form a MOF with kag topology, wherein the solvent comprises water only. Embodiments of the present disclosure also describe a method of capturing chemical species from a fluid composition comprising contacting a MOF composition with kag topology and pore size of about 3.4Å to 4.8Å with a fluid composition comprising two or more chemical species and capturing one or more captured chemical species from the fluid composition.

Mesospheric H2O and H2O2 densities inferred from in situ positive ion composition measurement

Science.gov (United States)

Kopp, E.

1984-01-01

A model for production and loss of oxonium ions in the high-latitude D-region is developed, based on the observed excess of 34(+) which has been interpreted as H2O2(+). The loss mechanism suggested in the study is the attachment of N2 and/or CO2 in three-body reactions. Furthermore, mesospheric water vapor and H2O2 densities are inferred from measurements of four high-latitude ion compositions, based on the oxonium model. Mixing ratios of hydrogen peroxide of up to two orders of magnitude higher than previous values were obtained. A number of reactions, reaction constants, and a block diagram of the oxonium ion chemistry in the D-region are given.

SnTe-TiC-C composites as high-performance anodes for Li-ion batteries

Science.gov (United States)

Son, Seung Yeon; Hur, Jaehyun; Kim, Kwang Ho; Son, Hyung Bin; Lee, Seung Geol; Kim, Il Tae

2017-10-01

Intermetallic SnTe composites dispersed in a conductive TiC/C hybrid matrix are synthesized by high-energy ball milling (HEBM). The electrochemical performances of the composites as potential anodes for Li-ion batteries are evaluated. The structural and morphological characteristics of the SnTe-TiC-C composites with various TiC contents are investigated by X-ray diffraction (XRD) and high-resolution transmission electron microscopy, which reveal that SnTe and TiC are uniformly dispersed in a carbon matrix. The electrochemical performance is significantly improved by introducing TiC to the SnTe-C composite; higher TiC contents result in better performances. Among the prepared composites, the SnTe-TiC (30%)-C and SnTe-TiC (40%)-C electrodes exhibit the best electrochemical performance, showing the reversible capacities of, respectively, 652 mAh cm-3 and 588 mAh cm-3 after 400 cycles and high rate capabilities with the capacity retentions of 75.4% for SnTe-TiC (30%)-C and 82.2% for SnTe-TiC (40%)-C at 10 A g-1. Furthermore, the Li storage reaction mechanisms of Te or Sn in the SnTe-TiC-C electrodes are confirmed by ex situ XRD.

One-step synthesis of continuous free-standing Carbon Nanotubes-Titanium oxide composite films as anodes for lithium-ion batteries

International Nuclear Information System (INIS)

Gao, Hongxu; Hou, Feng; Wan, Zhipeng; Zhao, Sha; Yang, Deming; Liu, Jiachen; Guo, Anran; Gong, Yuxuan

2015-01-01

Highlights: • CNTs/TiO 2 compoiste films synthesized are continuous and free-standing. • The film can be directly used as flexible, binder-free Lithium-Ion Battery electrode. • The CNTs/TiO 2 electrodes exhibit excellent rate capacity and cyclic stability. • Our strategy is readily applicable to fabricate other CNTs-based composite films. - Abstract: Continuous free-standing Carbon Nanotubes (CNTs)/Titanium oxide (TiO 2 ) composite films were fabricated in a vertical CVD gas flow reactor with water sealing by the One-Step Chemical Vapor Deposition (CVD) approach. The composite films consist of multiple layers of conductive carbon nanotube networks with titanium oxide nanoparticles decorating on carbon nanotube surface. The as-synthesized flexible and transferrable composite films show excellent electrochemical properties, when the content of tetrabutyl titanate is 19.0 wt.%, which can be promising as binder-free anodes for Lithium-Ion Battery (LIB) applications. It demonstrates remarkably high rate capacity of 150 mAh g −1 , as well as excellent high rate cyclic stability over 500 cycles (current density of 3000 mA g −1 ). Such observations can be attributed to the relatively larger surface area and pore volume comparing with pristine CNT films. Great potentials of CNTs/TiO 2 composite films for large-scale production and application in energy devices were shown

Predicting Upscaled Behavior of Aqueous Reactants in Heterogeneous Porous Media

Science.gov (United States)

Wright, E. E.; Hansen, S. K.; Bolster, D.; Richter, D. H.; Vesselinov, V. V.

2017-12-01

When modeling reactive transport, reaction rates are often overestimated due to the improper assumption of perfect mixing at the support scale of the transport model. In reality, fronts tend to form between participants in thermodynamically favorable reactions, leading to segregation of reactants into islands or fingers. When such a configuration arises, reactions are limited to the interface between the reactive solutes. Closure methods for estimating control-volume-effective reaction rates in terms of quantities defined at the control volume scale do not presently exist, but their development is crucial for effective field-scale modeling. We attack this problem through a combination of analytical and numerical means. Specifically, we numerically study reactive transport through an ensemble of realizations of two-dimensional heterogeneous porous media. We then employ regression analysis to calibrate an analytically-derived relationship between reaction rate and various dimensionless quantities representing conductivity-field heterogeneity and the respective strengths of diffusion, reaction and advection.

Mass-producible method for preparation of a carbon-coated graphite@plasma nano-silicon@carbon composite with enhanced performance as lithium ion battery anode

International Nuclear Information System (INIS)

Chen, Hedong; Wang, Zhoulu; Hou, Xianhua; Fu, Lijun; Wang, Shaofeng; Hu, Xiaoqiao; Qin, Haiqing; Wu, Yuping

2017-01-01

Carbon-coated core-shell structure artificial graphite@plasma nano-silicon@carbon (AG@PNSi@C) composite, applying as lithium ion battery anode material, has been prepared via spray drying method. The plasma nano-silicon (<100 nm), which contained amorphous silicon, was synthesized by radio frequency induction plasma system with the high temperatures processing capability and high quench rates. The artificial graphite in the composite acts as the core which supports the particle and provides electroconductivity, while PNSi attached on the surface of the core, enhances the specific capacity of the composite. The as prepared composite shows superior performance as anode in lithium-ion batteries, regarding to the initial Coulombic efficiency and cycle life. The initial Coulombic efficiency of AG@PNSi@C electrode is 81.0% with a discharge capacity of 553 mAh g −1 and a recharge capacity of 448 mAh g −1 . During cycling, AG@PNSi@C exhibits excellent performance with a very low capacity fading that the discharge capacity maintains 498.2 mAh g −1 and 449.4 mAh g −1 after 250 cycles and 500 cycles. AG@PNSi@C also shows enhanced resistance against high current density. Besides the remarkable electrochemical performances, the facile and mass-producible synthesis process makes the AG@PNSi@C composite very promising for its application in lithium-ion batteries.

Facile Synthesis of Graphene/ZnO Composite as an Anode with Enhanced Performance for Lithium Ion Batteries

Directory of Open Access Journals (Sweden)

Yanhong Zhao

2014-01-01

Full Text Available Graphene/ZnO composites with different contents of ZnO have been successfully synthesized via a liquid phase route. The structure, morphology, and electrochemical performances of the composites are investigated by XRD, Raman, SEM, TEM, AFM, and electrochemical measurement. The results reveal that ZnO nanoparticles wedged on the surface of the graphene nanosheets. The initial capacity of graphene/ZnO (1 : 1 reached 1155.27 mAh g−1, which increased 162.87 mAh g−1 compared with the initial capacity of graphene. This could be attributed to the unique structure of the prepared composite and synergies of graphene and ZnO in the lithium ion storage.

Composition and energy spectrum variations of auroral ions

International Nuclear Information System (INIS)

Lynch, J.; Leach, R.; Pulliam, D.; Scherb, F.

1977-01-01

We have detected H + ,O + , and He ++ ions with E/q up to 20 keV/charge in a hydrogen aurora over Churchill, Manitoba, during the flight of a Javelin sounding rocket on February 11, 1975, We observed several examples of different types of ion events. One type consisted of bursts of H + and O + ions which arrived simultaneously at all energies within the range of the E/q analyzer. These events were apparently of local origin (distance + ions (O + /H + approximately-greater-than30%). A second type of event consisted of bursts of enhanced H + counting rates but no O + ions. The dispersion in time of the energy spectrum was consistent with an injection and acceleration site located at about 20 R/sub E/ from the earth. An enhancement of the He ++ counting rates was associated with these events, but the He ++ data are of limited statistical significance. A third type of event, consisting of short bursts of H + ions with wide energy spreads, was observed in association with an event in which the energy of the H + ions showed time dispersion. We interpret these short H + bursts as due to ions trapped in traveling waves generated by an explosive injection of plasma in the earth's magnetotail

The formation of urea in space. I. Ion-molecule, neutral-neutral, and radical gas-phase reactions

Science.gov (United States)

Brigiano, Flavio Siro; Jeanvoine, Yannick; Largo, Antonio; Spezia, Riccardo

2018-02-01

Context. Many organic molecules have been observed in the interstellar medium thanks to advances in radioastronomy, and very recently the presence of urea was also suggested. While those molecules were observed, it is not clear what the mechanisms responsible to their formation are. In fact, if gas-phase reactions are responsible, they should occur through barrierless mechanisms (or with very low barriers). In the past, mechanisms for the formation of different organic molecules were studied, providing only in a few cases energetic conditions favorable to a synthesis at very low temperature. A particularly intriguing class of such molecules are those containing one N-C-O peptide bond, which could be a building block for the formation of biological molecules. Urea is a particular case because two nitrogen atoms are linked to the C-O moiety. Thus, motivated also by the recent tentative observation of urea, we have considered the synthetic pathways responsible to its formation. Aims: We have studied the possibility of forming urea in the gas phase via different kinds of bi-molecular reactions: ion-molecule, neutral, and radical. In particular we have focused on the activation energy of these reactions in order to find possible reactants that could be responsible for to barrierless (or very low energy) pathways. Methods: We have used very accurate, highly correlated quantum chemistry calculations to locate and characterize the reaction pathways in terms of minima and transition states connecting reactants to products. Results: Most of the reactions considered have an activation energy that is too high; but the ion-molecule reaction between NH2OHNH2OH2+ and formamide is not too high. These reactants could be responsible not only for the formation of urea but also of isocyanic acid, which is an organic molecule also observed in the interstellar medium.

Design and Synthesis of SnO_2 Nanosheets/Nickel/Polyvinylidene Fluoride Ternary Composite as Free-standing, Flexible Electrode for Lithium Ion Batteries

International Nuclear Information System (INIS)

Zhang, Yan; Xiao, Qizhen; Lei, Gangtie; Li, Zhaohui; Li, Xiaojing

2015-01-01

In this report, we have designed a novel SnO_2 nanosheets/nickel/polyvinylidene fluoride ternary composite as anode materials for lithium ion batteries. The SnO_2 nanosheets are uniformly coated on the surface of nickel/polyvinylidene fluoride conductive fiber, as confirmed by XRD, SEM, and TEM characterizations. As an anode material for lithium ion batteries, this as-prepared ternary composite delivers a high capacity of 865.4 mAh g"−"1 at 200 mA g"−"1 after 60 cycles. Furthermore, the SnO_2 in this composite material exhibits a good capacity retention as well as rate capability. This result indicates the completely reversible reaction between Li_4_._4Sn and SnO_2, greatly improving the specific capacity of SnO_2. The ternary SnO_2/Ni/PVDF composite limits the volume expansion on lithium insertion, and buffer spaces during charge/discharge, resulting in the excellent cyclic performances.

Evaluation of CNTs/MnO{sub 2} composite for adsorption of {sup 60}Co(II), {sup 65}Zn(II) and Cd(II) ions from aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Sharaf El-Deen, Sahar E.A.; Moussa, Saber I.; Mekawy, Zakaria A.; Shehata, Mohamed K.K.; Someda, Hanan H. [Atomic Energy Authority, Inshas (Egypt). Dept. of Nuclear Chemistry; Sadeek, Sadeek A. [Zagazig Univ. (Egypt). Dept. of Chemistry

2017-03-01

CNTs/MnO{sub 2} composite was synthesized by a co-precipitation method after preparation of carbon nanotubes (CNTs) using a chemical oxidation method and was characterized using Fourier transformer infrared (FT-IR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The synthesized CNTs/MnO{sub 2} composite was used as a sorbent for the removal of some radionuclides ({sup 60}Co and {sup 65}Zn-radioisotopes) and Cd (II) ions from aqueous solutions. Different parameters affecting the removal process including pH, contact time and metal ion concentration were investigated. Isotherm and kinetic models were studied. Adsorption data was interpreted in terms of both Freundlich and Langmuir isotherms and indicated that the CNTs/MnO{sub 2} composite complied well with both Langmuir and Freundlich models for {sup 60}Co and Cd(II) ions and with the Freundlich model only for the {sup 65}Zn radioisotope. A pseudo-second-order model was effectively employed to describe the adsorption behavior of {sup 60}Co, {sup 65}Zn and Cd(II) ions. Desorption of {sup 60}Co and {sup 65}Zn and Cd(II) ions from loaded samples was studied using different eluents.

Dynamic model of ion and water transport in ionic polymer-metal composites

Directory of Open Access Journals (Sweden)

Zicai Zhu

2011-12-01

Full Text Available In the process of electro-mechanical transduction of ionic polymer-metal composites (IPMCs, the transport of ion and water molecule plays an important role. In this paper, the theoretical transport models of IPMCs are critically reviewed, with particular emphasis on the recent developments in the latest decade. The models can be divided into three classes, thermodynamics of irreversible process model, frictional model and Nernst-Planck (NP equation model. To some extent the three models can be transformed into each other, but their differences are also obvious arising from the various mechanisms that considered in different models. The transport of ion and water molecule in IPMCs is compared with that in membrane electrode assembly and electrodialysis membrane to identify and clarify the fundamental transport mechanisms in IPMCs. And an improved transport model is proposed and simplified for numerical analysis. The model considers the convection effect rather than the diffusion as the major transport mechanism, and both the self-diffusion and the electroosmosis drag are accounted for in the water flux equation.

Ion Implantation of Polymers

DEFF Research Database (Denmark)

Popok, Vladimir

2012-01-01

The current paper presents a state-of-the-art review in the field of ion implantation of polymers. Numerous published studies of polymers modified by ion beams are analysed. General aspects of ion stopping, latent track formation and changes of structure and composition of organic materials...... are discussed. Related to that, the effects of radiothermolysis, degassing and carbonisation are considered. Specificity of depth distributions of implanted into polymers impurities is analysed and the case of high-fluence implantation is emphasised. Within rather broad topic of ion bombardment, the focus...... is put on the low-energy implantation of metal ions causing the nucleation and growth of nanoparticles in the shallow polymer layers. Electrical, optical and magnetic properties of metal/polymer composites are under the discussion and the approaches towards practical applications are overviewed....

Ion-exchange composite membranes pore-filled with sulfonated poly(ether ether ketone) and Engelhard titanosilicate-10 for improved performance of vanadium redox flow batteries

Science.gov (United States)

Kim, Jihoon; Lee, Yongkyu; Jeon, Jae-Deok; Kwak, Seung-Yeop

2018-04-01

A series of ion-exchange membranes for vanadium redox flow batteries (VRBs) are prepared by filling the pores of a poly(tetrafluoroethylene) (PTFE) substrate with sulfonated poly(ether ether ketone) (SPEEK) and microporous Engelhard titanosilicate-10 (ETS-10). The effects of ETS-10 incorporation and PTFE reinforcement on membrane properties and VRB single-cell performance are investigated using various characterization tools. The results show that these composite membranes exhibit improved mechanical properties and reduced vanadium-ion permeabilities owing to the interactions between ETS-10 and SPEEK, the suppressed swelling of PTFE, and the unique ETS-10 framework. The composite membrane with 3 wt% ETS-10 (referred to as "SE3/P") exhibits the best membrane properties and highest ion selectivity. The VRB system with the SE3/P membrane exhibits higher cell capacity, higher cell efficiency, and lower capacity decay than that with a Nafion membrane. These results indicate that this composite membrane has potential as an alternative to Nafion in VRB systems.

Journal of Chemical Sciences | Indian Academy of Sciences

Indian Academy of Sciences (India)

Excited state intramolecular charge transfer reaction of 4-(morpholenyl) benzonitrile in solution: Effects ... in (mixed solvent + electrolyte) systems: Role of reactant-solvent and reactant-ion interactions .... A molecular dynamics simulation study.

Self-organizing nanodot structures on InP surfaces evolving under low-energy ion irradiation: analysis of morphology and composition.

Science.gov (United States)

Radny, Tobias; Gnaser, Hubert

2014-01-01

Surfaces of InP were bombarded by 1.9 keV Ar(+) ions under normal incidence. The total accumulated ion fluence Φ the samples were exposed to was varied from 1 × 10(17) cm(-2) to 3 × 10(18) cm(-2), and ion fluxes f of (0.4 - 2) × 10(14) cm(-2) s(-1) were used. The surface morphology resulting from these ion irradiations was examined by atomic force microscopy (AFM). Generally, nanodot structures are formed on the surface; their dimensions (diameter, height and separation), however, were found to depend critically on the specific bombardment conditions. As a function of ion fluence, the mean radius r, height h, and spacing l of the dots can be fitted by power-law dependences: r ∝ Φ(0.40), h ∝ Φ(0.48), and l ∝ Φ(0.19). In terms of ion flux, there appears to exist a distinct threshold: below f ~ (1.3 ± 0.2) × 10(14) cm(-2) s(-1), no ordering of the dots exists and their size is comparatively small; above that value of f, the height and radius of the dots becomes substantially larger (h ~ 40 nm and r ~ 50 nm). This finding possibly indicates that surface diffusion processes could be important. In order to determine possible local compositional changes in these nanostructures induced by ion impact, selected samples were prepared for atom probe tomography (APT). The results indicate that APT can provide analytical information on the composition of individual InP nanodots. By means of 3D APT data, the surface region of such nanodots evolving under ion bombardment could be examined with atomic spatial resolution. At the InP surface, the values of the In/P concentration ratio are distinctly higher over a distance of approximately 1 nm and amount to 1.3 to 1.7.

Time resolved FTIR study of the catalytic CO oxidation under periodic variation of the reactant concentration

Energy Technology Data Exchange (ETDEWEB)

Kritzenberger, J; Wokaun, A [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

1997-06-01

Oxidation of CO over palladium/zirconia catalyst obtained from an amorphous Pd{sub 25}Zr{sub 75} precursor was investigated by time resolved FTIR spectroscopy. Sine wave shaped modulation of the reactant concentration, i.e. variation of CO or O{sub 2} partial pressure, was used to induce variations of the IR signals of product (CO{sub 2}) and unconverted reactant (CO), which were detected in a multi-pass absorption cell. The phase shift {phi} between external perturbation and variation of the CO{sub 2} signal was examined in dependence on temperature (100{sup o}C{<=}T{<=}350{sup o}C) and modulation frequency (1.39x10{sup -4}Hz{<=}{omega}{<=}6.67x10{sup -2}Hz). From the phase shift values, a simple Eley-Rideal mechanism is excluded, and the rate limiting step of the Langmuir-Hinshelwood mechanism for the CO oxidation may be identified. Adsorption and possible surface movement of CO to the actual reaction site determine the rate of the CO oxidation on the palladium/zirconia catalyst used in our study. The introduction of an external perturbation is a first step towards the application of two-dimensional infrared spectroscopy to heterogeneous catalyzed reactions. (author) 3 figs., 4 refs.

Assembly of core–shell structured porous carbon–graphene composites as anode materials for lithium-ion batteries

International Nuclear Information System (INIS)

Guo, Rong; Zhao, Li; Yue, Wenbo

2015-01-01

As potential anode materials for lithium-ion batteries, mesoporous carbons such as CMK-3 and CMK-8 usually show stable cycling performances but only slightly higher reversible capacities than commercial graphite. Graphene has much higher theoretical capacity than that of graphite in theory. However, its electrochemical behavior is not as good as expected due to the aggregation of graphene nanosheets. Herein we describe a novel strategy for the preparation of core–shell structured porous carbon–graphene composites. Compared to pure porous carbons or pure graphene nanosheets, these novel composites exhibit superior electrochemical performances including higher reversible capacities and better cycle/rate performances. This core–shell structure can avoid the aggregation of graphene nanosheets as well as may stabilize the mesostructure of porous carbon, which is beneficial to improving the electrochemical performances of the composites

Effects of dual-ion irradiation on the swelling of SiC/SiC composites

International Nuclear Information System (INIS)

Kishimoto, Hirotatsu; Kohyama, Akira; Ozawa, Kazumi; Kondo, Sosuke

2005-01-01

Silicon carbide (SiC) matrix composites reinforced by SiC fibers is a candidate structural material of fusion gas-cooled blanket system. From the viewpoint of material designs, it is important to investigate the swelling by irradiation, which results from the accumulation of displacement damages. In the fusion environment, (n, α) nuclear reactions are considered to produce helium gas in SiC. For the microstructural evolution, a dual-ion irradiation method is able to simulate the effects of helium. In the present research, 1.7 MeV tandem and 1 MeV single-end accelerators were used for Si self-ion irradiation and helium implantation, respectively. The average helium over displacement per atom (dpa) ratio in SiC was adjusted to 60 appm/dpa. The irradiation temperature ranged from room temperature to 1400degC. The irradiation-induced swelling was measured by the step height method. Helium that was implanted simultaneously with displacement damages in dual-ion irradiated SiC increased the swelling that was larger than that by single-ion irradiated SiC below 800degC. Since this increase was not observed above 1000degC, the interaction of helium and displacement damages was considered to change above 800degC. In this paper, the microstructural behavior and dimensional stability of SiC materials under the fusion relevant environment are discussed. (author)

Comparison of direct and alternating current vacuum ultraviolet lamps in atmospheric pressure photoionization.

Science.gov (United States)

Vaikkinen, Anu; Haapala, Markus; Kersten, Hendrik; Benter, Thorsten; Kostiainen, Risto; Kauppila, Tiina J

2012-02-07

A direct current induced vacuum ultraviolet (dc-VUV) krypton discharge lamp and an alternating current, radio frequency (rf) induced VUV lamp that are essentially similar to lamps in commercial atmospheric pressure photoionization (APPI) ion sources were compared. The emission distributions along the diameter of the lamp exit window were measured, and they showed that the beam of the rf lamp is much wider than that of the dc lamp. Thus, the rf lamp has larger efficient ionization area, and it also emits more photons than the dc lamp. The ionization efficiencies of the lamps were compared using identical spray geometries with both lamps in microchip APPI mass spectrometry (μAPPI-MS) and desorption atmospheric pressure photoionization-mass spectrometry (DAPPI-MS). A comprehensive view on the ionization was gained by studying six different μAPPI solvent compositions, five DAPPI spray solvents, and completely solvent-free DAPPI. The observed reactant ions for each solvent composition were very similar with both lamps except for toluene, which showed a higher amount of solvent originating oxidation products with the rf lamp than with the dc lamp in μAPPI. Moreover, the same analyte ions were detected with both lamps, and thus, the ionization mechanisms with both lamps are similar. The rf lamp showed a higher ionization efficiency than the dc lamp in all experiments. The difference between the lamp ionization efficiencies was greatest when high ionization energy (IE) solvent compositions (IEs above 10 eV), i.e., hexane, methanol, and methanol/water, (1:1 v:v) were used. The higher ionization efficiency of the rf lamp is likely due to the larger area of high intensity light emission, and the resulting larger efficient ionization area and higher amount of photons emitted. These result in higher solvent reactant ion production, which in turn enables more efficient analyte ion production. © 2012 American Chemical Society

Composite gel polymer electrolyte for lithium ion batteries

Science.gov (United States)

Naderi, Roya

Composite gel polymer electrolyte (CGPE) films, consisting of poly (vinylidene fluoride-hexafluoropropylene) (PVdF-HFP) as the membrane, DMF and PC as solvent and plasticizing agent, mixture of charge modified TiO2 and SiO 2 nano particles as ionic conductors, and LiClO4+LiPF 6 as lithium salts were fabricated. Following the work done by Li et al., CGPE was coated on an O2-plasma treated trilayer polypropylene-polyethylene-polypropylene membrane separator using solution casting technique in order to improve the adhesive properties of gel polymer electrolyte to the separator membrane and its respective ionic conductivity due to decreasing the bulk resistance. In acidic CGPE with, the mixture of acid treated TiO2 and neutral SiO2 nano particles played the role of the charge modified nano fillers with enhanced hydroxyl groups. Likely, the mixture of neutral TiO 2 nano particles with basic SiO2 prepared through the hydrolization of tetraethyl orthosilicate (TEOS) provided a more basic environment due to the residues of NH4OH (Ammonium hydroxide) catalyst. The O2 plasma treated separator was coated with the solution of PVDF-HFP: modified nano fillers: Organic solvents with the mixture ratio of 0.1:0.01:1. After the evaporation of the organic solvents, the dried coated separator was soaked in PC-LiClO4+LiPF6 in EC: DMC:DEC (4:2:4 in volume) solution (300% wt. of PVDF-HFP) to form the final CGPE. Lim et al. has reported the enhanced ionic conductivity of 9.78*10-5 Scm-1 in an acidic composite polystyrene-Al2O3 solid electrolyte system with compared to that of basic and neutral in which the ionic conductivity undergoes an ion hopping process in solid interface rather than a segmental movement of ions through the plasticized polymer chain . Half-cells with graphite anode and Li metal as reference electrode were then assembled and the electrochemical measurements and morphology examinations were successfully carried out. Half cells demonstrated a considerable change in their

General theory of the multistage geminate reactions of the isolated pairs of reactants. II. Detailed balance and universal asymptotes of kinetics.

Science.gov (United States)

Kipriyanov, Alexey A; Doktorov, Alexander B

2014-10-14

The analysis of general (matrix) kinetic equations for the mean survival probabilities of any of the species in a sample (or mean concentrations) has been made for a wide class of the multistage geminate reactions of the isolated pairs. These kinetic equations (obtained in the frame of the kinetic approach based on the concept of "effective" particles in Paper I) take into account various possible elementary reactions (stages of a multistage reaction) excluding monomolecular, but including physical and chemical processes of the change in internal quantum states carried out with the isolated pairs of reactants (or isolated reactants). The general basic principles of total and detailed balance have been established. The behavior of the reacting system has been considered on macroscopic time scales, and the universal long-term kinetics has been determined.

Near Earth Inner-Source and Interstellar Pickup Ions Observed with the Hot Plasma Composition Analyzer of the Magnetospheric Multiscale Mission Mms-Hpca

Science.gov (United States)

Gomez, R. G.; Fuselier, S. A.; Mukherjee, J.; Gonzalez, C. A.

2017-12-01

Pickup ions found near the earth are generally picked up in the rest frame of the solar wind, and propagate radially outward from their point of origin. While propagating, they simultaneously gyrate about the magnetic field. Pickup ions come in two general populations; interstellar and inner source ions. Interstellar ions originate in the interstellar medium, enter the solar system in a neutral charge state, are gravitationally focused on the side of the sun opposite their arrival direction and, are ionized when they travel near the sun. Inner-source ions originate at a location within the solar system and between the sun and the observation point. Both pickup ion populations share similarities in composition and charge states, so measuring of their dynamics, using their velocity distribution functions, f(v)'s, is absolutely essential to distinguishing them, and to determining their spatial and temporal origins. Presented here will be the results of studies conducted with the four Hot Plasma Composition Analyzers of the Magnetospheric Multiscale Mission (MMS-HPCA). These instruments measure the full sky (4π steradians) distribution functions of near earth plasmas at a 10 second cadence in an energy-to-charge range 0.001-40 keV/e. The instruments are also capable of parsing this combined energy-solid angle phase space with 22.5° resolution polar angle, and 11.25° in azimuthal angle, allowing for clear measurement of the pitch angle scattering of the ions.

Chemical composition of sublates (difficultly soluble substances) which form on interaction of polyvalent metal ions with potassium alkylcarboxylate

International Nuclear Information System (INIS)

Skrylev, L.D.; Skryleva, T.L.; Sazonova, V.F.

1996-01-01

The pH value is considered for its effect on chemical composition of sublates which form on interaction of fatty acid collectors (potassium alkylcarboxylate) with polyvalent ions of Ni, An, Cu and Be. It is shown that interaction of these ions with fatty acid collectors in weakly acid, neutral and weakly alkaline solutions is accompanied by formation of medium soaps. Acid soaps are formed in more acid solutions, while in more alkaline-basic soaps. Domains of stability for medium soaps of Ni, Zn, Cu and Be are determined. 17 refs.; 4 figs

Observations of Heavy Ions in the Magnetosphere

Science.gov (United States)

Kistler, L. M.

2017-12-01

There are two sources for the hot ions in the magnetosphere: the solar wind and the ionosphere. The solar wind is predominantly protons, with about 4% He++ and less than 1% other high charge state heavy ions. The ionospheric outflow is also predominantly H+, but can contain a significant fraction of heavy ions including O+, N+, He+, O++, and molecular ions (NO+, N2+, O2+). The ionospheric outflow composition varies significantly both with geomagnetic activity and with solar EUV. The variability in the contribution of the two sources, the variability in the ionospheric source itself, and the transport paths of the different species are all important in determining the ion composition at a given location in the magnetosphere. In addition to the source variations, loss processes within the magnetosphere can be mass dependent, changing the composition. In particular, charge exchange is strongly species dependent, and can lead to heavy ion dominance at some energies in the inner magnetosphere. In this talk we will review the current state of our understanding of the composition of the magnetosphere and the processes that determine it.

Towards better description of solar activity variation in the International Reference Ionosphere topside ion composition model

Czech Academy of Sciences Publication Activity Database

Truhlík, Vladimír; Bilitza, D.; Třísková, Ludmila

2015-01-01

Roč. 55, č. 8 (2015), s. 2099-2105 ISSN 0273-1177 R&D Projects: GA MŠk(CZ) LH11123 Institutional support: RVO:68378289 Keywords : ion composition * topside ionosphere * solar activity * empirical model * International Reference Ionosphere Subject RIV: BL - Plasma and Gas Discharge Physics Impact factor: 1.409, year: 2015 http://www.sciencedirect.com/science/article/pii/S027311771400489X

Solid-state photoelectrochemical H2 generation with gaseous reactants

International Nuclear Information System (INIS)

Iwu, Kingsley O.; Galeckas, Augustinas; Kuznetsov, Andrej Yu.; Norby, Truls

2013-01-01

Photocurrent and H 2 production were demonstrated in an all solid-state photoelectrochemical cell employing gaseous methanol and water vapour at the photoanode. Open circuit photovoltage of around −0.4 V and short circuit photocurrent of up to 250 μA/cm 2 were obtained. At positive bias, photocurrent generation was limited by the irradiance, i.e., the amount of photogenerated charge carriers at the anode. Time constants and impedance spectra showed an electrochemical capacitance of the cell of about 15 μF/cm 2 in the dark, which increased with increasing irradiance. With only water vapour at the anode, the short circuit photocurrent was about 6% of the value with gaseous methanol and water vapour. The photoanode and electrocatalyst on carbon paper support were affixed to the proton conducting membrane using Nafion ® as adhesive, an approach that yielded photocurrents up to 15 times better than that of a cell assembled by hot-pressing, in spite of the overall cell resistance of the latter being up to five times less than that of the former. This is attributed, at least partially, to reactants being more readily available at the photoanode of the better performing cell

Low energy ion scattering (LEIS) and the compositional and structural analysis of solid surfaces

International Nuclear Information System (INIS)

Berg, J.A. van den; Armour, D.G.

1981-01-01

The physics of Low Energy Ion Scattering (LEIS) and its application as a surface analytical technique are reviewed. It is shown that compositional and short-range structural information can be obtained by choosing experimental conditions which optimize the contributions of single and double (or multiple) collisions, respectively. The LEIS technique allows mass analysis in a straightforward way, possesses a high surface selectivity but is unable to provide quantitative information in isolation due to scattering cross-section uncertainties and not easily quantifiable charge exchange effects. Structural information regarding adsorbate positions on single crystal surfaces and the short-range substrate structure (including damaged and reconstructed surfaces) can be obtained by exploiting shadowing and/or multiple scattering phenomena. The progress made in recent years in this area is charted. It is shown that computer simulations often play an important role in this type of study. Effects, such as charge exchange, inelastic energy loss and ion beam surface perturbations, which complicate the use of low energy ion scattering for surface analysis are discussed in detail. The present status of the technique in the different areas of study is indicated. (author)

A Cadmium Ion-selective Membrane Electrode Based on Strong Acidic Organic-inorganic Composite Cation-exchanger: Polyaniline Ce(IV Molybdate

Directory of Open Access Journals (Sweden)

Syed Ashfaq NABI

2008-05-01

Full Text Available A cadmium ion-selective composite cation-exchanger polyaniline Ce(IV molybdate was used as electroactive component for the construction of a ion-selective membrane electrode. The membrane electrode showed a Nerstian response for Cd(II ions over a wide concentration range 5 × 10-6 – 1 × 10-1 with a sub-Nerstian slope of 27 mV per decade change in concentration of cadmium ions. The limit of detection was also ascertained to be 5 × 10-6 M. It has a fast response time 15 s and can be very well utilized for more than three months with out any appreciable divergence in potentials. The optimum pH for the smooth functioning of this electrode was found to be in the Ph range of 2.5 – 7.5. The electrode also showed better selectivity for Cd(II ions over many other interfering ions. The practical utility of membrane electrode was demonstrated by using as indicator electrode for the potentiometric titration of Cd(II with EDTA and determination of cadmium content in drain water.

Preparation of unidirectional fiber reinforced tantalum carbide composites

International Nuclear Information System (INIS)

Newkirk, L.R.; Riley, R.E.; Sheinberg, H.; Valencia, F.A.; Wallace, T.C.

1979-01-01

A process is described for uniformly infiltrating 3000 filament carbon yarn with Ta and subsequent densification by hot pressing. Ta deposition rate is characterized as a function of deposition temperature, reactant flows, yarn pull rate, and coating chamber geometry for yarn pull rates from 2 to 50 m/h and Ta loadings from 40 to 350 wt % gain. Densification procedures for unidirectional pressings are described and data is presented which shows significant improvement in flexure strength over conventional TaC-C powder composites

Application of ion implantation in stevia breeding

International Nuclear Information System (INIS)

Wang Cailian; Chen Qiufang; Jin Wei; Lu Ting; Shu Shizhen

1999-08-01

Dry seed of stevia were implanted with 60-100 keV nitrogen ion and 75 keV carbon ion of various doses, and the effects of the composition and yield of stevioside were studied. The results showed that ion beam could induce variation in total stevioside yield and the composition of the plant. The best treatment was 75 keV nitrogen ion with 5 x 10 14 N + /cm 2 , the stevioside yield and Rebaudioside A (R-A) content were increased by 4.74% and 14.08% respectively. The effects induced by implantation of carbon ion were higher than those induced by implantation of nitrogen ion. Effects of Feng 1 x Ri Yuan and Ri Yuan x Feng 2 are higher than those of Ji Ning and Feng 2 . Seven mutation lines were selected from the mutation progenies. The stevioside composition of these lines were previously improved. The results suggest a potential application of ion implantation in stevia breeding

Applications of ion scattering in surface analysis

International Nuclear Information System (INIS)

Armour, D.G.

1981-01-01

The study of ion scattering from surfaces has made an increasingly important contribution both to the development of highly surface specific analysis techniques and to the understanding of the atomic collision processes associated with ion bombardment of solid surfaces. From an analysis point of view, by appropriate choice of parameters such as ion energy and species, scattering geometry and target temperature, it is possible to study not only the composition of the surface layer but also the detailed atomic arrangement. The ion scattering technique is thus particularly useful for the study of surface compositional and structural changes caused by adsorption, thermal annealing or ion bombardment treatments of simple or composite materials. Ion bombardment induced desorption, damage or atomic mixing can also be effectively studied using scattering techniques. By reviewing the application of the technique to a variety of these technologically important surface investigations, it is possible to illustrate the way in which ion scattering has developed as the understanding of the underlying physics has improved. (author)

Electrochemical investigation of MoTe2/rGO composite materials for sodium-ion battery application

Science.gov (United States)

Panda, Manas Ranjan; Anish Raj, K.; Sarkar, Ananta; Bao, Qiaoliang; Mitra, Sagar

2018-05-01

2D layered materials are found to be promising anode materials for renewable energy storage devices like sodium and Li-ion batteries and have become attractive options due to their high specific capacity, abundance and low cost. In this work, we synthesized 2D MoTe2 layers embedded in reduced graphene oxide (rGO) anode material for sodium-ion battery applications. 2D MoTe2 was prepared by a solid-state reaction in vacuum at a temperature of 800 °C. The prepared composite material MoTe2/rGO showed excellent electrochemical performance against the sodium metal. The discharge capacity of MoTe2/rGO was observed to be 280 mAh g-1 at a current rate of 1.0 A g-1 for 100 cycles. rGO plays an important role in embedding the MoTe2 structure, thus improving the electrical and mechanical properties, leading to a superior cycling stability and excellent electrochemical performances of MoTe2 for sodium-ion battery applications.

Synthesis of LiFePO4/Graphene Nano composite and Its Electrochemical Properties as Cathode Material for Li-Ion Batteries

International Nuclear Information System (INIS)

Ma, X.; Chen, G.; Liu, Q.; Zeng, G.; Wu, T.

2014-01-01

LiFePO 4 /graphene nano composite was successfully synthesized by rheological phase method and its electrochemical properties as the cathode materials for lithium ion batteries were measured. As the iron source in the synthesis, FeOOH nano rods anchored on graphene were first synthesized. The FeOOH nano rods precursors and the final LiFePO 4 /graphene nano composite products were characterized by XRD, SEM, and TEM. While the FeOOH precursors were nano rods with 5-10 nm in diameter and 10-50 nm in length, the LiFePO 4 were nanoparticles with 20-100 nm in size. Compared with the electrochemical properties of LiFePO 4 particles without graphene nano sheets, it is clear that the graphene nano sheets can improve the performances of LiFePO 4 as the cathode material for lithium ion batteries. The as-synthesized LiFePO 4 /graphene nano composite showed high capacities and good cyclabilities. When measured at room temperature and at the rate of 0.1 C (1 C = 170 mA g -1 ), the composite showed a discharge capacity of 156 mA h g -1 in the first cycle and a capacity retention of 96% after 15 cycles. The improved performances of the composite are believed to be the result of the three-dimensional conducting network formed by the flexible and planar graphene nano sheets.

Synthesis and electrochemical characterization of mesoporous Li2FeSiO4/C composite cathode material for Li-ion batteries

Science.gov (United States)

Kumar, Ajay; Jayakumar, O. D.; Bazzi, Khadije; Nazri, Gholam-Abbas; Naik, Vaman M.; Naik, Ratna

2015-03-01

Lithium iron silicate (Li2FeSiO4) has the potential as cathode for Li ion batteries due to its high theoretical capacity (~ 330 mAh/g) and improved safety. The application of Li2FeSiO4 as cathode material has been challenged by its poor electronic conductivity and slow lithium ion diffusion in the solid phase. In order to solve these problems, we have synthesized mesoporous Li2FeSiO4/C composites by sol-gel method using the tri-block copolymer (P123) as carbon source. The phase purity and morphology of the composite materials were characterized by x-ray diffraction, SEM and TEM. The XRD pattern confirmed the formation of ~ 12 nm size Li2FeSiO4 crystallites in composites annealed at 600 °C for 6 h under argon atmosphere. The electrochemical properties are measured using the composite material as positive electrode in a standard coin cell configuration with lithium as the active anode and the cells were tested using AC impedance spectroscopy, cyclic voltammetry, and galvanostatic charge/discharge cycling. The Li2FeSiO4/C composites showed a discharge capacity of ~ 240 mAh/g at a rate of C/30 at room temperature. The effect of different annealing temperature and synthesis time on the electrochemical performance of Li2FeSiO4/C will be presented.

Preparation and characterization of flake graphite/silicon/carbon spherical composite as anode materials for lithium-ion batteries

International Nuclear Information System (INIS)

Lai Jun; Guo Huajun; Wang Zhixing; Li Xinhai; Zhang Xiaoping; Wu Feixiang; Yue Peng

2012-01-01

Highlights: ► Flake graphite/silicon/carbon composite is synthesized via spray drying. ► Flake graphite of ∼0.5 μm and glucose are used to prepare the composite. ► The as-prepared composite shows spherical and porous appearance. ► The composite shows nearly the same cycleability as commercial graphite in 20 cycles. ► The composite shows a reversible capacity of 552 mAh/g at the 20th cycle. - Abstract: Using nano-Si, glucose and flake graphite of ∼0.5 μm as raw materials, flake graphite/silicon/carbon composite is successfully synthesized via spray drying and subsequent pyrolysis. The samples are characterized by XRD, SEM, TEM and electrochemical measurements. The composite is composed of flake graphite, nano-Si and amorphous glucose-pyrolyzed carbon and presents good spherical appearance. Some micron pores arising from the decomposition of glucose exist on the surface of the composite particles. The composite has a high reversible capacity of 602.7 mAh/g with an initial coulombic efficiency of 69.71%, and shows nearly the same cycleability as the commercial graphite in 20 cycles. Both the glucose-pyrolyzed carbon and the micron pores play important roles in improving the cycleability of the composite. The flake graphite/silicon/carbon composite electrode is a potential alternative to graphite for high energy-density lithium ion batteries.

Effect of reactant concentration on the structural properties of hydrothermally-grown ZnO rods on seed-layer ZnO / polyethylene terephthalate substrates

Energy Technology Data Exchange (ETDEWEB)

Jeong, Y. I.; Shin, C. M.; Heo, J. H.; Ryu, H. [Inje University, Gimhae (Korea, Republic of); Lee, W. J. [Dong-Eui University, Busan (Korea, Republic of); Son, C. S. [Silla University, Busan (Korea, Republic of); Choi, H. [Pukyong National University, Busan (Korea, Republic of)

2011-09-15

The morphology and the structural properties were studied for zinc-oxide (ZnO) rods hydrothermally grown on seed-layer ZnO/polyethylene terephthalate (PET) substrates at various reactant concentrations. Dissolved solutions with de-ionized water, zinc nitrate hexahydrate (Zn(NO{sub 3}){sub 2}{center_dot}6H{sub 2}O, ZNH) and hexamethylenetetramine (C{sub 6}H{sub 12}N{sub 4}, HMT) were employed as reactants for hydrothermal growth of ZnO. The transparency of the mixtures (ZNH+HMT) with increasing reactant concentration from 0.025 to 0.25 M changed from transparent to translucent to opaque (white colors) due to Zn(OH){sub 2} precipitates. When the concentration was increased, the density of the ZnO rods increased, and the morphology of the ZnO rods changed from a hexagonal flat-end shape to a sharp-end or flake-like structure. The sharp-end rods with increasing concentration from 0.1 to 0.15 M resulted from the etching process at a lower pH condition (less than pH 6) after the ZnO rod growth, and the flake-like structure was due to a high growth rate. The ZnO seed layer might have improved the alignment of ZnO rods and made a high density of ZnO rods. In addition, the structural properties were improved at lower concentrations by inserting a seed layer.

In situ synthesis of α-MoO3/graphene composites as anode materials for lithium ion battery

International Nuclear Information System (INIS)

Liu, Chun-Ling; Wang, Yan; Zhang, Chen; Li, Xiao-Shan; Dong, Wen-Sheng

2014-01-01

The α-MoO 3 /graphene composites (MoO 3 /G) were prepared via an in situ hydrothermal synthesis. The composites were characterized using various characterization techniques including powder X-ray diffraction, transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, and the electrochemical performance test. The results show that these MoO 3 /G composites exhibit high capacity and good cycle stability when used as the lithium-ion battery anode. Among all the samples, the MoO 3 /G-27 reveals the best electrochemical performance with an initial charge capacity of 977.7 mAh g −1 at a current density of 50 mA g −1 , the first coulombic efficiency of 69.5%. After eighty cycles the electrode still maintains a capacity of 869.2 mAh g −1 , giving high capacity retention of 88.9%. The good electrochemical performance of the composite anode is close related to its structure, in which the MoO 3 nanobelts are not only homogeneously anchored on the surface but also embedded in the interlayer of the graphene sheets; hence the volume change and aggregation of the MoO 3 nanobelts during lithium ion insertion/extraction process can be effectively hindered. On the other hand, graphene itself is an electronic conductor; the graphene and MoO 3 nanobelts connect closely, which offers large electrode/electrolyte contacting area, short path length for Li + transporting during lithium insertion and extraction. - Highlights: • The α-MoO 3 /graphene composites were prepared via an in situ hydrothermal synthesis. • The MoO 3 /G-27 anode delivers an initial reversible capacity of 977.7 mAh g −1 . • After 80 cycles it has a reversible capacity of 869.2 mAh g −1 at 50 mA g −1

Liquid-liquid extraction of ion-association complexes of cobalt(II-4-(2-pyridylazoresorcinol with ditetrazolium salts

Directory of Open Access Journals (Sweden)

Divarova Vidka V.

2015-01-01

Full Text Available The formation and liquid-liquid extraction of ion-association complexes between Co(II-4-(2-Pyridylazoresorcinol (PAR anionic chelates and cations of three ditetrazolium chlorides were studied: Blue Tetrazolium chloride (BTC, Neotetrazolium chloride (NTC and Nitro Blue Tetrazolium chloride (NBT. The optimum conditions for the formation and solvent extraction of the ion-association comlpex chelates were determined. It has been found that in the systems of Co(II-PAR-DTS, the reactants are reacted in molar ratios 1:2:1 and the general formula of complexes was suggested. The extraction equilibria were investigated and quantitatively characterized by the equilibrium constants and the recovery factors. The analytical characteristics of the complexes were calculated.

Inorganic ion composition in Tardigrada

DEFF Research Database (Denmark)

Halberg, Kenneth Agerlin; Larsen, Kristine Wulff; Jørgensen, Aslak

2013-01-01

are indicative of a powerful ion-retentive mechanism in Tardigrada. Moreover, our data indicate that cryptobiotic tardigrades contain a large fraction of unidentified organic osmolytes, the identification of which is expected to provide increased insight into the phenomenon of cryptobiosis....

Composite materials obtained by the ion-plasma sputtering of metal compound coatings on polymer films

Science.gov (United States)

Khlebnikov, Nikolai; Polyakov, Evgenii; Borisov, Sergei; Barashev, Nikolai; Biramov, Emir; Maltceva, Anastasia; Vereshchagin, Artem; Khartov, Stas; Voronin, Anton

2016-01-01

In this article, the principle and examples composite materials obtained by deposition of metal compound coatings on polymer film substrates by the ion-plasma sputtering method are presented. A synergistic effect is to obtain the materials with structural properties of the polymer substrate and the surface properties of the metal deposited coatings. The technology of sputtering of TiN coatings of various thicknesses on polyethylene terephthalate films is discussed. The obtained composites are characterized by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), atomic force microscopy (AFM), and scanning tunneling microscopy (STM) is shown. The examples of application of this method, such as receiving nanocomposite track membranes and flexible transparent electrodes, are considered.

A mesoporous WO{sub 3−X}/graphene composite as a high-performance Li-ion battery anode

Energy Technology Data Exchange (ETDEWEB)

Liu, Fei [C-Industry Incubation Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon 305-600 (Korea, Republic of); Kim, Jong Gu [C-Industry Incubation Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon 305-600 (Korea, Republic of); Department of Fine Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Lee, Chul Wee [C-Industry Incubation Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon 305-600 (Korea, Republic of); University of Science and Technology (UST), Gajeong-ro, Yuseong-gu, Daejeon 305-333 (Korea, Republic of); Im, Ji Sun, E-mail: jsim@krict.re.kr [C-Industry Incubation Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon 305-600 (Korea, Republic of); University of Science and Technology (UST), Gajeong-ro, Yuseong-gu, Daejeon 305-333 (Korea, Republic of)

2014-10-15

Graphical abstract: The highly flexible and conductive graphene layer can enhance electron transfer, protect metal oxides against disintegration and aggregation and buffer the strain induced by volume expansion during cycles. The mesoporous surface layer provides an open network for Li+ diffusion. - Highlights: • Novel cocktail effects of 2D mesoporous WO{sub 3−X}/graphene for lithium ion battery. • New approach for lithium ion battery by easy and unique synthesis method. • Mechanism study with proper data for understanding a reaction on anode surface. - Abstract: A novel mesoporous WO{sub 3−X}/graphene composite was developed. This material allowed rapid electron and Li{sup +} ion diffusion when used as a Li-ion battery (LIB) anode material. Remarkably, the graphene support protected WO{sub 3−X} from changing volume during the electrochemical cycling process; this process generally induces capacity loss. The current work describes a high-performance anode material for LIB that has highly dense WO{sub 3−X}, as well as high capacity, rate capability and stability.

Comparison of H+ and He+ Plasmapause Locations Based on Resurrected and Reevaluated OGO-5 Ion Composition Data Base

Science.gov (United States)

Truhlik, Vladimir; Triskova, Ludmila; Benson, Robert F.; Bilitza, Dieter; Grebowsky, Joseph; Richards, Phil G.; Smilauer, Jan

2014-01-01

Orbiting Geophysical Observatory 5 (OGO 5) magnetospheric ion-composition data (H+, He+ and O+) from an ion spectrometer (Sharp, 1969) have been retrieved from old magnetic tapes archived at the National Space Science Data Center (NSSDC). The highly compressed binary format was converted into a user-friendly ASCII format and these data have been made available online. We have inspected reliability and consistency of this data set in state of the art current knowledge. Comparing with the climatological model IRI-2012 and the mathematical model FLIP a shift of absolute and relative ion densities with time was revealed. We have suggested a correction procedure of individual H+, He+ and O+ ion densities. Using the corrected data set, we investigated plasmapause locations based on density gradient in H+, and He+. Correlation coefficient of both locations was determined as approx. 0.886 and the typical difference (Delta)L approx. 0.1. The electron density at the He+ plasmapause location for all cases is >100/cu cm.

Electrochemical characteristics of nc-Si/SiC composite for anode electrode of lithium ion batteries

International Nuclear Information System (INIS)

Jeon, Bup Ju; Lee, Joong Kee

2014-01-01

Graphical abstract: Cycling performances and coulombic efficiencies of the nc-Si/SiC composite anodes at different CH 4 /SiH 4 mole ratios. -- Highlights: • Our work has focused on irreversible discharge capacity and capacity retention of nc-Si/SiC composite particles. • Particles comprised a mixed construction of nc-Si/SiC structure with dual phases. • The SiC phase acted as retarding media, leading to enhanced cycle stability. -- Abstract: nc-Si/SiC composite particles were prepared as an anode material for lithium ion batteries using a plasma jet with DC arc discharge. The composition of the nc-Si/SiC composite particles was controlled by setting the mole ratio of CH 4 and SiH 4 precursor gases. X-ray diffraction, TEM images, and Raman shift analyses revealed that the synthesized nc-Si/SiC composite particles comprised a construction of nano-nocaled structure with crystalline phases of active silicon, highly disordered amorphous carbon of graphite and crystalline phases of β-SiC. In the experimental range examined, the nc-Si/SiC composite particles showed good coulombic efficiency in comparison with particles high Si–Si bonding content due to the interplay of particles with a small proportion of carbon and the buffering effect against volume expansion by structural stabilization, and played a role as retarding media for the rapid electrochemical reactions of the SiC crystal against lithium

Electrochemical characteristics of nc-Si/SiC composite for anode electrode of lithium ion batteries

Energy Technology Data Exchange (ETDEWEB)

Jeon, Bup Ju [Department of Energy Resources, Shinhan University, 233-1, Sangpae-dong, Dongducheon, Gyeonggi-do, 483-777 (Korea, Republic of); Lee, Joong Kee, E-mail: leejk@kist.re.kr [Advanced Energy Materials Processing Laboratory, Center for Energy Convergence Research, Green City Technology Institute, Korea Institute of Science and Technology, Hwarangno 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of)

2014-03-25

Graphical abstract: Cycling performances and coulombic efficiencies of the nc-Si/SiC composite anodes at different CH{sub 4}/SiH{sub 4} mole ratios. -- Highlights: • Our work has focused on irreversible discharge capacity and capacity retention of nc-Si/SiC composite particles. • Particles comprised a mixed construction of nc-Si/SiC structure with dual phases. • The SiC phase acted as retarding media, leading to enhanced cycle stability. -- Abstract: nc-Si/SiC composite particles were prepared as an anode material for lithium ion batteries using a plasma jet with DC arc discharge. The composition of the nc-Si/SiC composite particles was controlled by setting the mole ratio of CH{sub 4} and SiH{sub 4} precursor gases. X-ray diffraction, TEM images, and Raman shift analyses revealed that the synthesized nc-Si/SiC composite particles comprised a construction of nano-nocaled structure with crystalline phases of active silicon, highly disordered amorphous carbon of graphite and crystalline phases of β-SiC. In the experimental range examined, the nc-Si/SiC composite particles showed good coulombic efficiency in comparison with particles high Si–Si bonding content due to the interplay of particles with a small proportion of carbon and the buffering effect against volume expansion by structural stabilization, and played a role as retarding media for the rapid electrochemical reactions of the SiC crystal against lithium.

Scanning ion microscopy with low energy lithium ions

International Nuclear Information System (INIS)

Twedt, Kevin A.; Chen, Lei; McClelland, Jabez J.

2014-01-01

Using an ion source based on photoionization of laser-cooled lithium atoms, we have developed a scanning ion microscope with probe sizes of a few tens of nanometers and beam energies from 500 eV to 5 keV. These beam energies are much lower than the typical operating energies of the helium ion microscope or gallium focused ion beam systems. We demonstrate how low energy can be advantageous in ion microscopy when detecting backscattered ions, due to a decreased interaction volume and the potential for surface sensitive composition analysis. As an example application that demonstrates these advantages, we non-destructively image the removal of a thin residual resist layer during plasma etching in a nano-imprint lithography process. - Highlights: • We use an ion source based on photoionization of laser-cooled lithium atoms. • The ion source makes possible a low energy (500 eV to 5 keV) scanning ion microscope. • Low energy is preferred for ion microscopy with backscattered ions. • We use the microscope to image a thin resist used in nano-imprint lithography

The structural and compositional analysis of single crystal surfaces using low energy ion scattering

International Nuclear Information System (INIS)

Armour, D.G.; Van der Berg, J.A.; Verheij, IL.K.

1979-01-01

The use of ion scattering for surface composition and structure analysis has been reviewed. The extreme surface specificity of this technique has been widely used to obtain quitative information in a straightforward way, but the/aolc/currence of charge exchange processes, thermal lattice vibrations and multiple scattering have precluded quantitative analysis of experimental data. Examples are quoted to illustrate the progress that has been made in understanding these fundamental processes and in applying this knowledge to the development of the analytical capabilities of the technique. (author)

Negative ion formation in collisions involving excited alkali atoms

International Nuclear Information System (INIS)

Cheret, M.

1988-01-01

Ion-pair production is considered as the prototype of the crossing problem between potential energy curves. In general an alkali atom is one of the reactants the other being an halogen, hydrogen atom or molecule. Experimental results are generally analyzed in the framework of the Landau-Zener-Stuekelberg theory, ionization potential and electron affinity, being the most important parameters. In order to vary these parameters over a wide range two experimental works have been devoted to systems of excited alkali atoms colliding with ground state alkali atoms. In the first study Rb atoms are excited to various ns or nd states from Rb(5d) to Rb(9s) in a cell. The second study is devoted to the Na(3p)-Na(3s) system, in this study also the possibility of creating excited negative ions (Na - (3s3p)) has been investigated. These results are presented and analyzed. Finally further developments of the subject are suggested. 17 refs.; 8 figs.; 1 table

Investigation of the stability of glass-ceramic composites containing CeTi2O6 and CaZrTi2O7 after ion implantation

Science.gov (United States)

Paknahad, Elham; Grosvenor, Andrew P.

2017-12-01

Glass-ceramic composite materials have been investigated for nuclear waste sequestration applications due to their ability to incorporate large amounts of radioactive waste elements. A key property that needs to be understood when developing nuclear waste sequestration materials is how the structure of the material responds to radioactive decay of nuclear waste elements, which can be simulated by high energy ion implantation. Borosilicate glass-ceramic composites containing brannerite-type (CeTi2O6) or zirconolite-type (CaZrTi2O7) oxides were synthesized at different annealing temperatures and investigated after being implanted with high-energy Au ions to mimic radiation induced structural damage. Backscattered electron (BSE) images were collected to investigate the interaction of the brannerite crystallites with the glass matrix before and after implantation and showed that the morphology of the crystallites in the composite materials were not affected by radiation damage. Surface sensitive Ti K-edge glancing angle XANES spectra collected from the implanted composite materials showed that the structures of the CeTi2O6 and CaZrTi2O7 ceramics were damaged as a result of implantation; however, analysis of Si L2,3-edge XANES spectra indicated that the glass matrix was not affected by ion implantation.

Investigation of the stability of glass-ceramic composites containing CeTi 2 O 6 and CaZrTi 2 O 7 after ion implantation

Energy Technology Data Exchange (ETDEWEB)

Paknahad, Elham; Grosvenor, Andrew P.

2017-12-01

Glass-ceramic composite materials have been investigated for nuclear waste sequestration applications due to their ability to incorporate large amounts of radioactive waste elements. A key property that needs to be understood when developing nuclear waste sequestration materials is how the structure of the material responds to radioactive decay of nuclear waste elements, which can be simulated by high energy ion implantation. Borosilicate glass-ceramic composites containing brannerite-type (CeTi2O6) or zirconolite-type (CaZrTi2O7) oxides were synthesized at different annealing temperatures and investigated after being implanted with high-energy Au ions to mimic radiation induced structural damage. Backscattered electron (BSE) images were collected to investigate the interaction of the brannerite crystallites with the glass matrix before and after implantation and showed that the morphology of the crystallites in the composite materials were not affected by radiation damage. Surface sensitive Ti K-edge glancing angle XANES spectra collected from the implanted composite materials showed that the structures of the CeTi2O6 and CaZrTi2O7 ceramics were damaged as a result of implantation; however, analysis of Si L2,3-edge XANES spectra indicated that the glass matrix was not affected by ion implantation.

Chemical composition of waterfall-induced air ions: Spectrometry vs. simulations

Energy Technology Data Exchange (ETDEWEB)

Parts, T.-E.; Luts, A. [Tartu Univ. (Estonia). Dept. of Environmental Physics; Laakso, L.; Hirsikko, A.; Groenholm, T.; Kulmala, M. [Helsinki Univ. (Finland). Dept. of Physical Sciences

2007-07-01

Our measurements of ion size distributions near a waterfall provided new evidence for a waterfall-induced modification of air ion sizes. The ion size spectrum near a waterfall permanently differs from that in ordinary tropospheric air. In this paper we investigated the near-waterfall air ions chemical nature in detail. We carried out a simulation series of air small negative ion evolution, proposing that falling water, as a new environmental component, increases the concentration of OH{sup -} cluster ions. The produced OH{sup -} ions were employed as an extra input for our ion evolution model. The presence of additional OH{sup -} ions resulted in a decrease of typically model-provided NO{sub 3}{sup -} and/or HSO{sub 4}{sup -} cluster ion concentrations and an increase of the abundance of HCO{sub 3}{sup -} cluster ions. Near the waterfall the latter ions became dominant in our simulations. (orig.)

Composite media for ion processing

Science.gov (United States)

Mann, Nick R [Blackfoot, ID; Wood, Donald J [Peshastin, WA; Todd, Terry A [Aberdeen, ID; Sebesta, Ferdinand [Prague, CZ

2009-12-08

Composite media, systems, and devices for substantially removing, or otherwise processing, one or more constituents of a fluid stream. The composite media comprise a plurality of beads, each having a matrix substantially comprising polyacrylonitrile (PAN) and supporting one or more active components which are effective in removing, by various mechanisms, one or more constituents from a fluid stream. Due to the porosity and large surface area of the beads, a high level of contact is achieved between composite media of the present invention and the fluid stream being processed. Further, the homogeneity of the beads facilitates use of the beads in high volume applications where it is desired to effectively process a large volume of flow per unit of time.

Evaluation of the effect of reactant gases mass flow rates on power density in a polymer electrolyte membrane fuel cell

Science.gov (United States)

Kahveci, E. E.; Taymaz, I.

2018-03-01

In this study it was experimentally investigated the effect of mass flow rates of reactant gases which is one of the most important operational parameters of polymer electrolyte membrane (PEM) fuel cell on power density. The channel type is serpentine and single PEM fuel cell has an active area of 25 cm2. Design-Expert 8.0 (trial version) was used with four variables to investigate the effect of variables on the response using. Cell temperature, hydrogen mass flow rate, oxygen mass flow rate and humidification temperature were selected as independent variables. In addition, the power density was used as response to determine the combined effects of these variables. It was kept constant cell and humidification temperatures while changing mass flow rates of reactant gases. From the results an increase occurred in power density with increasing the hydrogen flow rates. But oxygen flow rate does not have a significant effect on power density within determined mass flow rates.

The effects of reactants ratios, reaction temperatures and times on Maillard reaction products of the L-ascorbic acid/L-glutamic acid system

Directory of Open Access Journals (Sweden)

Yong-Yan ZHOU

2016-01-01

Full Text Available Abstract The transformation law of the Maillard reaction products with three different reactants ratios - equimolar reactants, excess L-glutamic acid and excess L-ascorbic acid reaction respectively, five different temperatures, and different time conditions for the L-ascorbic acid / L-glutamic acid system were investigated. Results showed that, the increase of the reaction time and temperature led to the increase of the browning products, uncoloured intermediate products, as well as aroma compounds. Compared with the equimolar reaction system, the excess L-ascorbic acid reaction system produced more browning products and uncoloured intermediate products, while the aroma compounds production remained the same. In the excess L-glutamic acid system, the uncoloured intermediate products increased slightly, the browning products remained the same, while the aroma compounds increased.

Structural and compositional characterization of LiNbO{sub 3} crystals implanted with high energy iron ions

Energy Technology Data Exchange (ETDEWEB)

Sada, C., E-mail: cinzia.sada@unipd.i [Universita di Padova and CNISM, Dipartimento di Fisica, Via Marzolo 8, 35131 Padova (Italy); Argiolas, N.; Bazzan, M.; Ciampolillo, M.V.; Zaltron, A.M.; Mazzoldi, P. [Universita di Padova and CNISM, Dipartimento di Fisica, Via Marzolo 8, 35131 Padova (Italy); Agarwal, D.C.; Avastshi, D.K. [Inter-University Accelerator Centre, Post Box-10502, New Delhi 110067 (India)

2010-10-01

Iron ions were implanted with a total fluence of 6 x 10{sup 17} ions/m{sup 2} into lithium niobate crystals by way of a sequential implantation at different energies of 95, 100 and 105 MeV respectively through an energy retarder Fe foil to get a uniform Fe doping of about few microns from the surface. The implanted crystals were then annealed in air in the range 200-400 {sup o}C for different durations to promote the crystalline quality that was damaged by implantation. In order to understand the basic phenomena underlying the implantation process, compositional in-depth profiles obtained by the secondary ion mass spectrometry were correlated to the structural properties of the implanted region measured by the high resolution X-ray diffraction depending on the process parameters. The optimised preparation conditions are outlined in order to recover the crystalline quality, essential for integrated photorefractive applications.

A compact high resolution ion mobility spectrometer for fast trace gas analysis.

Science.gov (United States)

Kirk, Ansgar T; Allers, Maria; Cochems, Philipp; Langejuergen, Jens; Zimmermann, Stefan

2013-09-21

Drift tube ion mobility spectrometers (IMS) are widely used for fast trace gas detection in air, but portable compact systems are typically very limited in their resolving power. Decreasing the initial ion packet width improves the resolution, but is generally associated with a reduced signal-to-noise-ratio (SNR) due to the lower number of ions injected into the drift region. In this paper, we present a refined theory of IMS operation which employs a combined approach for the analysis of the ion drift and the subsequent amplification to predict both the resolution and the SNR of the measured ion current peak. This theoretical analysis shows that the SNR is not a function of the initial ion packet width, meaning that compact drift tube IMS with both very high resolution and extremely low limits of detection can be designed. Based on these implications, an optimized combination of a compact drift tube with a length of just 10 cm and a transimpedance amplifier has been constructed with a resolution of 183 measured for the positive reactant ion peak (RIP(+)), which is sufficient to e.g. separate the RIP(+) from the protonated acetone monomer, even though their drift times only differ by a factor of 1.007. Furthermore, the limits of detection (LODs) for acetone are 180 pptv within 1 s of averaging time and 580 pptv within only 100 ms.

Formation of tin-tin oxide core–shell nanoparticles in the composite SnO{sub 2−x}/nitrogen-doped carbon nanotubes by pulsed ion beam irradiation

Energy Technology Data Exchange (ETDEWEB)

Korusenko, P.M., E-mail: korusenko@obisp.oscsbras.ru [Omsk Scientific Center, Siberian Branch of the Russian Academy of Sciences, Karl Marx avenue 15, 644040 Omsk (Russian Federation); Nesov, S.N.; Bolotov, V.V.; Povoroznyuk, S.N. [Omsk Scientific Center, Siberian Branch of the Russian Academy of Sciences, Karl Marx avenue 15, 644040 Omsk (Russian Federation); Pushkarev, A.I. [National Research Tomsk Polytechnic University, Lenin Ave. 2a, 634028 Tomsk (Russian Federation); Ivlev, K.E. [Omsk Scientific Center, Siberian Branch of the Russian Academy of Sciences, Karl Marx avenue 15, 644040 Omsk (Russian Federation); Smirnov, D.A. [St. Petersburg State University, Lieutenant Shmidt Emb. 11, 198504 St. Petersburg (Russian Federation); Institute of Solid State Physics, Dresden University of Technology, D-01069 Dresden (Germany)

2017-03-01

Highlights: • Original method the formation of core–shell structures by pulsed ion beam is proposed. • The composite SnO{sub 2−x}/N-MWCNTs was irradiated by pulsed ion beam. • Morphology and electronic structure of the irradiated composite were characterized. • The formation of Sn−SnO{sub x} core–shell nanoparticles after irradiation was observed. - Abstract: The complex methods of transmission electron microscopy, energy dispersive X-ray analysis, and X-ray photoelectron spectroscopy were used to investigate the changes in the morphology, phase composition, and electronic structure of the composite SnO{sub 2−x}/nitrogen-doped multiwalled carbon nanotubes (SnO{sub 2−x}/N-MWCNTs) irradiated with the pulsed ion beam of nanosecond duration. The irradiation of the composite SnO{sub 2−x}/N-MWCNTs leads to the formation of nanoparticles with the core–shell structure on the surface of CNTs with a sharp interfacial boundary. It has been established that the “core” is a metal tin (Sn{sup 0}) with a typical size of 5–35 nm, and the “shell” is a thin amorphous layer (2–6 nm) consisting of nonstoichiometric tin oxide with a low oxygen content. The “core–shell” structure Sn−SnO{sub x} is formed due to the process of heating and evaporation of SnO{sub 2−x} under the effect of the ion beam, followed by vapor deposition on the surface of carbon nanotubes.

Formation of nanodots and enhancement of thermoelectric power induced by ion irradiation in PbTe:Ag composite thin films

Energy Technology Data Exchange (ETDEWEB)

Bala, Manju, E-mail: manjubala474@gmail.com [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India); Meena, Ramcharan; Gupta, Srashti; Pannu, Compesh [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India); Tripathi, Tripurari S. [Aalto University, Värmemansgränden 2, 02150 Espoo (Finland); Varma, Shikha [Institute of Physics, Bhubaneshwar, Odisha 751005 (India); Tripathi, Surya K. [Department of Physics, Panjab University, Chandigarh 160 014 (India); Asokan, K., E-mail: asokaniuac@gmail.com [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India); Avasthi, Devesh K. [Amity University, Noida 201313, Uttar Pradesh (India)

2016-07-15

Present study demonstrates an enhancement in thermoelectric power of 10% Ag doped PbTe (PbTe:Ag) thin films when irradiated with 200 keV Ar ion. X-ray diffraction showed an increase in crystallinity for both PbTe and PbTe:10Ag nano-composite films after Ar ion irradiation due to annealing of defects in the grain boundaries. The preferential sputtering of Pb and Te ions in comparison to Ag ions resulted in the formation of nano-dots. This was further confirmed by X-ray photoelectron spectroscopy (XPS). Such an enhancement in thermoelectric power of irradiated PbTe:10Ag films in comparison to pristine PbTe:10Ag film is attributed to the decrease in charge carrier concentration that takes part in the transport process via restricting the tunneling of carriers through the wider potential barrier formed at the interface of nano-dots.

Ion structure and sequence of ion formation in acetylene flames

Energy Technology Data Exchange (ETDEWEB)

Larionova, I.A.; Fialkov, B.S.; Kalinich, K.YA.; Fialkov, A.B.; Ospanov, B.S.

1993-06-01

Results of a study of the ion composition of acetylene-air flames burning at low pressures are reported. Data on ion formation are compared for flames of saturated hydrocarbons, oxygen-containing fuels, and acetylene. It is shown that the characteristics of ion formation in the flame front and directly ahead of it are similar to those observed in flames of other fuels. These characteristics, however, are different in the low-temperature region. 9 refs.

Preparation and characterization of flake graphite/silicon/carbon spherical composite as anode materials for lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Lai Jun [School of Metallurgical Science and Engineering, Central South University, Changsha 410083 (China); Guo Huajun, E-mail: Lai_jun_@126.com [School of Metallurgical Science and Engineering, Central South University, Changsha 410083 (China); Wang Zhixing; Li Xinhai; Zhang Xiaoping; Wu Feixiang; Yue Peng [School of Metallurgical Science and Engineering, Central South University, Changsha 410083 (China)

2012-07-25

Highlights: Black-Right-Pointing-Pointer Flake graphite/silicon/carbon composite is synthesized via spray drying. Black-Right-Pointing-Pointer Flake graphite of {approx}0.5 {mu}m and glucose are used to prepare the composite. Black-Right-Pointing-Pointer The as-prepared composite shows spherical and porous appearance. Black-Right-Pointing-Pointer The composite shows nearly the same cycleability as commercial graphite in 20 cycles. Black-Right-Pointing-Pointer The composite shows a reversible capacity of 552 mAh/g at the 20th cycle. - Abstract: Using nano-Si, glucose and flake graphite of {approx}0.5 {mu}m as raw materials, flake graphite/silicon/carbon composite is successfully synthesized via spray drying and subsequent pyrolysis. The samples are characterized by XRD, SEM, TEM and electrochemical measurements. The composite is composed of flake graphite, nano-Si and amorphous glucose-pyrolyzed carbon and presents good spherical appearance. Some micron pores arising from the decomposition of glucose exist on the surface of the composite particles. The composite has a high reversible capacity of 602.7 mAh/g with an initial coulombic efficiency of 69.71%, and shows nearly the same cycleability as the commercial graphite in 20 cycles. Both the glucose-pyrolyzed carbon and the micron pores play important roles in improving the cycleability of the composite. The flake graphite/silicon/carbon composite electrode is a potential alternative to graphite for high energy-density lithium ion batteries.

Mesostructured niobium-doped titanium oxide-carbon (Nb-TiO2-C) composite as an anode for high-performance lithium-ion batteries

Science.gov (United States)

Hwang, Keebum; Sohn, Hiesang; Yoon, Songhun

2018-02-01

Mesostructured niobium (Nb)-doped TiO2-carbon (Nb-TiO2-C) composites are synthesized by a hydrothermal process for application as anode materials in Li-ion batteries. The composites have a hierarchical porous structure with the Nb-TiO2 nanoparticles homogenously distributed throughout the porous carbon matrix. The Nb content is controlled (0-10 wt%) to investigate its effect on the physico-chemical properties and electrochemical performance of the composite. While the crystalline/surface structure varied with the addition of Nb (d-spacing of TiO2: 0.34-0.36 nm), the morphology of the composite remained unaffected. The electrochemical performance (cycle stability and rate capability) of the Nb-TiO2-C composite anode with 1 wt% Nb doping improved significantly. First, a full cut-off potential (0-2.5 V vs. Li/Li+) of Nb-doped composite anode (1 wt%) provides a higher energy utilization than that of the un-doped TiO2-C anode. Second, Nb-TiO2-C composite anode (1 wt%) exhibits an excellent long-term cycle stability (100% capacity retention, 297 mAh/g at 0.5 C after 100 cycles and 221 mAh/g at 2 C after 500 cycles) and improved rate-capability (192 mAh/g at 5 C), respectively (1 C: 150 mA/g). The superior electrochemical performance of Nb-TiO2-C (1 wt%) could be attributed to the synergistic effect of improved electronic conductivity induced by optimal Nb doping (1 wt%) and lithium-ion penetration (high diffusion kinetics) through unique pore structures.

Ballistic Simulation Method for Lithium Ion Batteries (BASIMLIB) Using Thick Shell Composites (TSC) in LS-DYNA

Science.gov (United States)

2016-08-04

BAllistic SImulation Method for Lithium Ion Batteries (BASIMLIB) using Thick Shell Composites (TSC) in LS-DYNA Venkatesh Babu, Dr. Matt Castanier, Dr...and behavior of the cells through experimental and modeling at their crash worthiness laboratory • Most of the simulation work on the batteries are...at a single cell level and gap exists to simulate the batteries at their full pack capacity - Firstly, requires an enormous amount of computational

Electrospun LiFePO₄/C Composite Fiber Membrane as a Binder-Free, Self-Standing Cathode for Power Lithium-Ion Battery.

Science.gov (United States)

Chen, Li-Li; Shen, Xiang-Qian; Jing, Mao-Xiang; Zhu, Sheng-Wen; Pi, Zhi-Chao; Li, Jing-Quan; Zhai, Hong-Ai; Xiao, Ke-Song

2018-07-01

A LiFePO4/C composite fiber membrane was fabricated by the electrospinning method and subsequent thermal treatment. The thermal decomposition process was analyzed by TG/DSC, the morphology, microstructure and composition were studied using SEM, TEM, XRD, Raman, respectively. The results indicated that the prepared LiFePO4/C composite fibers were composed of nanosized LiFePO4 crystals and amorphous carbon coatings, which formed a three dimensional (3D) long-range networks, greatly enhanced the electronic conductivity of LiFePO4 electrode up to 3.59× 10-2 S · cm-2. The 3D LiFePO4/C fiber membrane could be directly used as a binder-free, self-standing cathode for lithium-ion battery, and exhibited an improved capacity and rate performance. The LiFePO4/C composite electrode delivered a discharge capacity of 116 mAh·g-1, 109 mAh·g-1, 103 mAh·g-1, 91 mAh·g-1, 80 mAh·g-1 at 0.1 C, 0.5 C, 1 C, 3 C, 5 C, respectively. And a stable cycling performance was also achieved that the specific capacity could retain 75 mA·g-1 after 500 cycles at 5 C. Therefore, this LiFePO4/C composite fiber membrane was promising to be used as a cathode for power lithium ion battery.

Hierarchical structured graphene/metal oxide/porous carbon composites as anode materials for lithium-ion batteries

International Nuclear Information System (INIS)

Guo, Rong; Yue, Wenbo; Ren, Yu; Zhou, Wuzong

2016-01-01

Highlights: • CeO 2 and Co 3 O 4 nanoparticles display different behavior within CMK-3. • CMK-3-CeO 2 and Co 3 O 4 show various electrochemical properties • CMK-3-CeO 2 and Co 3 O 4 are further wrapped by graphene nanosheets. • Graphene-encapsulated composites show better electrochemical performances. - Abstract: As a novel anode material for lithium-ion batteries, CeO 2 displays imperceptible volumetric and morphological changes during the lithium insertion and extraction processes, and thereby exhibits good cycling stability. However, the low theoretical capacity and poor electronic conductivity of CeO 2 hinder its practical application. In contrast, Co 3 O 4 possesses high theoretical capacity, but undergoes huge volume change during cycling. To overcome these issues, CeO 2 and Co 3 O 4 nanoparticles are formed inside the pores of CMK-3 and display various electrochemical behaviors due to the different morphological structures of CeO 2 and Co 3 O 4 within CMK-3. Moreover, the graphene/metal oxide/CMK-3 composites with a hierarchical structure are then prepared and exhibit better electrochemical performances than metal oxides with or without CMK-3. This novel synthesis strategy is hopefully employed in the electrode materials design for Li-ion batteries or other energy conversion and storage devices.

A highly stable (SnOx-Sn)@few layered graphene composite anode of sodium-ion batteries synthesized by oxygen plasma assisted milling

Science.gov (United States)

Cheng, Deliang; Liu, Jiangwen; Li, Xiang; Hu, Renzong; Zeng, Meiqing; Yang, Lichun; Zhu, Min

2017-05-01

The (SnOx-Sn)@few layered graphene ((SnOx-Sn)@FLG) composite has been synthesized by oxygen plasma-assisted milling. Owing to the synergistic effect of rapid plasma heating and ball mill grinding, SnOx (1 ≤ x ≤ 2) nanoparticles generated from the reaction of Sn with oxygen are tightly wrapped by FLG nanosheets which are simultaneously exfoliated from expanded graphite, forming secondary micro granules. Inside the granules, the small size of the SnOx nanoparticles enables the fast kinetics for Na+ transfer. The in-situ formed FLG and residual Sn nanoparticles improve the electrical conductivity of the composite, meanwhile alleviate the aggregation of SnOx nanoparticles and relieve the volume change during the cycling, which is beneficial for the cyclic stability for the Na+ storage. As an anode material for sodium-ion batteries, the (SnOx-Sn)@FLG composite exhibits a high reversible capacity of 448 mAh g-1 at a current density of 100 mA g-1 in the first cycle, with 82.6% capacity retention after 250 cycles. Even when the current density increases to 1000 mA g-1, this composite retains 316.5 mAh g-1 after 250 cycles. With superior Na+ storage stability, the (SnOx-Sn)@FLG composite can be a promising anode material for high performance sodium-ion batteries.

Electrodéposition de revêtements composites à base de polyaniline pour des applications de batterie Lithium-ion et de protection contre la corrosion

OpenAIRE

Harfouche , Nesrine

2016-01-01

In this study, we prepared two conductive composite materials based on polyaniline (PANI) byelectrodeposition. First, we investigated the development of new polyaniline/LiMn2O4 composite films forapplication as cathode material in lithium-ion batteries. Analysis by X-ray diffraction, EDS analysis and FTIRspectroscopy confirmed the incorporation of LiMn2O4 in composite films. The electrochemical analysis of thefilms obtained showed a higher conductivity of the composite films compared to the c...

Behaviour of tetraalkylammonium ions in high-field asymmetric waveform ion mobility spectrometry.

Science.gov (United States)

Aksenov, Alexander A; Kapron, James T

2010-05-30

High-field asymmetric waveform ion mobility spectrometry (FAIMS) is an ion-filtering technique recently adapted for use with liquid chromatography/mass spectrometry (LC/MS) to remove interferences during analysis of complex matrices. This is the first systematic study of a series of singly charged tetraalkylammonium ions by FAIMS-MS. The compensation voltage (CV) is the DC offset of the waveform which permits the ion to emerge from FAIMS and it was determined for each member of the series under various conditions. The electrospray ionization conditions explored included spray voltage, vaporizer temperature, and sheath and auxiliary gas pressure. The FAIMS conditions explored included carrier gas flow rate, electrode temperature and composition of the carrier gas. Optimum desolvation was achieved using sufficient carrier gas (flow rate > or = 2 L/min) to ensure stable response. Low-mass ions (m/z 100-200) are more susceptible to changes in electrode temperature and gas composition than high mass ions (m/z 200-700). As a result of this study, ions are reliably analyzed using standard FAIMS conditions (dispersion voltage -5000 V, carrier gas flow rate 3 L/min, 50% helium/50%nitrogen, inner electrode temperature 70 degrees C and outer electrode temperature 90 degrees C). Variation of FAIMS conditions may be of great use for the separation of very low mass tetraalkylammonium (TAA) ions from other TAA ions. The FAIMS conditions do not appear to have a major effect on higher mass ions. Copyright 2010 John Wiley & Sons, Ltd.

Cyclic performance tests of Sn/MWCNT composite lithium ion battery anodes at different temperatures

Energy Technology Data Exchange (ETDEWEB)

Tocoglu, U., E-mail: utocoglu@sakarya.edu.tr; Cevher, O.; Akbulut, H. [Sakarya University, Engineering Faculty, Department of Metallurgical and Materials Engineering, Esentepe Campus 54187 (Turkey)

2016-04-21

In this study tin-multi walled carbon nanotube (Sn-MWCNT) lithium ion battery anodes were produced and their electrochemical galvanostatic charge/discharge tests were conducted at various (25 °C, 35 °C, 50 °C) temperatures to determine the cyclic behaviors of anode at different temperatures. Anodes were produced via vacuum filtration and DC magnetron sputtering technique. Tin was sputtered onto buckypapers to form composite structure of anodes. SEM analysis was conducted to determine morphology of buckypapers and Sn-MWCNT composite anodes. Structural and phase analyses were conducted via X-ray diffraction and Raman Spectroscopy technique. CR2016 coin cells were assembled for electrochemical tests. Cyclic voltammetry test were carried out to determine the reversibility of reactions between anodes and reference electrode between 0.01-2.0 V potential window. Galvanostatic charge/discharge tests were performed to determine cycle performance of anodes at different temperatures.

Carbon Cryogel and Carbon Paper-Based Silicon Composite Anode Materials for Lithium-Ion Batteries

Science.gov (United States)

Woodworth, James; Baldwin, Richard; Bennett, William

2010-01-01

A variety of materials are under investigation for use as anode materials in lithium-ion batteries, of which, the most promising are those containing silicon. 6 One such material is a composite formed via the dispersion of silicon in a resorcinol-formaldehyde (RF) gel followed by pyrolysis. Two silicon-carbon composite materials, carbon microspheres and nanofoams produced from nano-phase silicon impregnated RF gel precursors have been synthesized and investigated. Carbon microspheres are produced by forming the silicon-containing RF gel into microspheres whereas carbon nano-foams are produced by impregnating carbon fiber paper with the silicon containing RF gel to create a free standing electrode. 1-5 Both materials have demonstrated their ability to function as anodes and utilize the silicon present in the material. Stable reversible capacities above 400 mAh/g for the bulk material and above 1000 mAh/g of Si have been observed.

Secondary ion mass spectroscopy (SIMS)

International Nuclear Information System (INIS)

Naik, P.K.

1975-01-01

Secondary Ion Mass Spectrometry (SIMS) which is primarily a method for investigating the chemical composition of the uppermost atomic layer of solid surfaces is explained. In this method, the specimen is bombarded with a primary positive ion beam of small current density monolayer. Positive and negative ions sputtered from the specimen are mass analysed to give the surface chemical composition. The analytical system which consists of a primary ion source, a target manipulator and a mass spectrometer housed in an ultrahigh vacuum system is described. This method can also be used for profile measurements in thin films by using higher current densities of the primary ions. Fields of application such as surface reactions, semiconductors, thin films emission processes, chemistry, metallurgy are touched upon. Various aspects of this method such as the sputtering process, instrumentation, and applications are discussed. (K.B.)

In-situ synthesis of monodisperse micro-nanospherical LiFePO4/carbon cathode composites for lithium-ion batteries

Science.gov (United States)

Gong, Hao; Xue, Hairong; Wang, Tao; He, Jianping

2016-06-01

The LiFePO4 is recognized as the promising cathode material, due to its high specific capacity, excellent, structural stability and environmental benignity. However, it is blamed for the low tap density and poor rate performance when served as the cathode materials for a long time. Here, the microspheric LiFePO4/C composites are successfully synthesized through a one-step in-situ solvothermal method combined with carbothermic reduction. These LiFePO4/C microspheres are assembled by LiFePO4 nanoparticles (∼100 nm) and uniformly coated by the carbon, which show a narrow diameter distribution of 4 μm. As a cathode material for lithium ion batteries, the LiFePO4/C composites can deliver an initiate charge capacity of 155 mAh g-1 and retain 90% of initial capacity after 200 cycles at 0.1 C. When cycled at high current densities up to 20 C, it shows a discharge capacity of ∼60 mAh g-1, exhibiting superior rate performance. The significantly improved electrochemical performance of LiFePO4/C composites material can be attributed to its special micro-nano hierarchical structure. Microspheric LiFePO4/C composites exhibit a high tap density about 1.3 g cm-3. What's more, the well-coated carbon insures the high electrical conductivity and the nano-sized LiFePO4/C particles shorten lithium ion transport, thus exhibiting the high specific capacity, high cycling stability and good rate performance.

Sputtering induced surface composition changes in copper-palladium alloys

International Nuclear Information System (INIS)

Sundararaman, M.; Sharma, S.K.; Kumar, L.; Krishnan, R.

1981-01-01

It has been observed that, in general, surface composition is different from bulk composition in multicomponent materials as a result of ion beam sputtering. This compositional difference arises from factors like preferential sputtering, radiation induced concentration gradients and the knock-in effect. In the present work, changes in the surface composition of copper-palladium alloys, brought about by argon ion sputtering, have been studied using Auger electron spectroscopy. Argon ion energy has been varied from 500 eV to 5 keV. Enrichment of palladium has been observed in the sputter-altered layer. The palladium enrichment at the surface has been found to be higher for 500 eV argon ion sputtering compared with argon ion sputtering at higher energies. Above 500 eV, the surface composition has been observed to remain the same irrespective of the sputter ion energy for each alloy composition. The bulk composition ratio of palladium to copper has been found to be linearly related to the sputter altered surface composition ratio of palladium to copper. These results are discussed on the basis of recent theories of alloy sputtering. (orig.)

Composition and stratigraphy of the paint layers: investigation on the Madonna dei Fusi by ion beam analysis techniques

Science.gov (United States)

Grassi, N.

2005-06-01

In the framework of the extensive study on the wood painting "Madonna dei fusi" attributed to Leonardo da Vinci, Ion Beam Analysis (IBA) techniques were used at the Florence accelerator laboratory to get information about the elemental composition of the paint layers. After a brief description of the basic principle and the general features of IBA techniques, we will illustrate in detail how the analysis allowed us to characterise the pigments of original and restored areas and the substrate composition, and to obtain information about the stratigraphy of the painting, also providing an estimate of the paint layer thickness.

Gold-coated silicon nanowire-graphene core-shell composite film as a polymer binder-free anode for rechargeable lithium-ion batteries

Science.gov (United States)

Kim, Han-Jung; Lee, Sang Eon; Lee, Jihye; Jung, Joo-Yun; Lee, Eung-Sug; Choi, Jun-Hyuk; Jung, Jun-Ho; Oh, Minsub; Hyun, Seungmin; Choi, Dae-Geun

2014-07-01

We designed and fabricated a gold (Au)-coated silicon nanowires/graphene (Au-SiNWs/G) hybrid composite as a polymer binder-free anode for rechargeable lithium-ion batteries (LIBs). A large amount of SiNWs for LIB anode materials can be prepared by metal-assisted chemical etching (MaCE) process. The Au-SiNWs/G composite film on current collector was obtained by vacuum filtration using an anodic aluminum oxide (AAO) membrane and hot pressing method. Our experimental results show that the Au-SiNWs/G composite has a stable reversible capacity of about 1520 mA h/g which was maintained for 20 cycles. The Au-SiNWs/G composite anode showed much better cycling performance than SiNWs/polyvinylidene fluoride (PVDF)/Super-P, SiNWs/G composite, and pure SiNWs anodes. The improved electrochemical properties of the Au-SiNWs/G composite anode material is mainly ascribed to the composite's porous network structure.

Carbon-covered Fe_3O_4 hollow cubic hierarchical porous composite as the anode material for lithium-ion batteries

International Nuclear Information System (INIS)

Chen, Shouhui; Zhou, Rihui; Chen, Yaqin; Fu, Yuanyuan; Li, Ping; Song, Yonghai; Wang, Li

2017-01-01

In this work, Prussian blue nanocrystals, a kind of cubic metal-organic frameworks, was firstly covered by a uniform layer of resorcinol-formaldehyde (RF) resin, and then followed with heat treatment at different pyrolysis temperatures. The effects of pyrolysis temperature on the morphologies, phase, pore size, and electrochemical performance of the pyrolysis products were studied in this work. The composite generated at 600 "∘C, FexC600, was a hollow cubic composite of Fe_3O_4 covered by a thin RF-derived carbon layer. The carbon layer on FexC600 was a robust and conductive protective layer, which can accommodate Fe_3O_4 NPs and withstand the huge volume change of Fe_3O_4 during the process of discharge and charge. When used as anodes for lithium-ion batteries, FexC600 showed excellent electrochemical performance. It delivered a discharge capacity of 1126 mAh g"−"1 with a coulombic efficiency of 98.8% at the current density of 100 mA g"−"1 after 100 times discharge/charge cycling. It even delivered a capacity of 492 mAh g"−"1 at the current density of 500 mA g"−"1. This cubic hollow composite would be a promising alternative anode material for lithium-ion batteries.

Kinetic Studies For the Removal of UO22+ and Pb2+ Ions From Aqueous Solution Using Zirconia Composite Material

International Nuclear Information System (INIS)

Sharaf El-Deen, G.E.

2008-01-01

Zirconia composite material was chemically synthesized previously and prepared by applying the sol-gel polymeric route using MgO as a stabilizer. The prepared composite material was characterized using various techniques: x-ray fluorescence (XRF), scanning electron microscope (SEM), differential thermal analysis and thermogravimetric analysis (DTA-TG), x-ray diffraction (XRD) and surface area using the BET-method. The sorption removal of UO 2 2+ and Pb 2+ ions from aqueous waste solution by zirconia composite material using batch technique was investigated. The sorption was carried out as a function of ph, particle size, shaking time and temperature. In this work, a comparison of kinetic models applied to the sorption process of each ion was evaluated for the pseudo first-order, the pseudo second-order, intra particle diffusion and homogeneous particle diffusion kinetic models, respectively. The results showed that the homogeneous particle diffusion model (HPDM) best correlate the experimental rate data and the numerical values of the rate constants and particle diffusion coefficients were determined from the graphical representation of the proposed models. Activation energy (Ε a ) and thermodynamic parameters of free energy (δ G * ), enthalpy (δ H * ) and entropy (δ S * ) of activation were also computed from the linearized form of Arrhenius equation

Li-ion batteries from LiFePO{sub 4} cathode and anatase/graphene composite anode for stationary energy storage

Energy Technology Data Exchange (ETDEWEB)

Choi, Daiwon; Wang, Donghai; Viswanathan, Vish V.; Wang, Wei; Nie, Zimin; Zhang, Ji-Guang; Graff, Gordon L.; Liu, Jun; Yang, Zhenguo [Pacific Northwest National Laboratory, 902 Battelle Boulevard, P.O. Box 999, Richland, WA 99352 (United States); Bae, In-Tae [Small Scale Systems Integration and Packaging Center, State University of New York at Binghamton, P.O. Box 6000, Binghamton, NY 13902 (United States); Duong, Tien [US Departments of Energy, 1000 Independence Ave., Washington, DC 20858 (United States)

2010-03-15

Li-ion batteries made from LiFePO{sub 4} cathode and anatase TiO{sub 2}/graphene composite anode were investigated for potential application in stationary energy storage. Fine-structured LiFePO{sub 4} was synthesized by a novel molten surfactant approach whereas anatase TiO{sub 2}/graphene nanocomposite was prepared via self-assembly method. The full cell that operated at 1.6 V demonstrated negligible fade even after more than 700 cycles at measured 1 C rate. While with relative lower energy density than traditional Li-ion chemistries interested for vehicle applications, the Li-ion batteries based on LiFePO{sub 4}/TiO{sub 2} combination potentially offers long life and low cost, along with safety, all which are critical to the stationary applications. (author)

CATALYST-FREE REACTIONS UNDER SOLVENT-FEE CONDITIONS: MICROWAVE-ASSISTED SYNTHESIS OF HETEROCYCLIC HYDRAZONES BELOW THE MELTING POINT OF NEAT REACTANTS: JOURNAL ARTICLE

Science.gov (United States)

NRMRL-CIN-1437 Jeselnik, M., Varma*, R.S., Polanc, S., and Kocevar, M. Catalyst-free Reactions under Solvent-fee Conditions: Microwave-assisted Synthesis of Heterocyclic Hydrazones below the Melting Point of Neat Reactants. Published in: Chemical Communications 18:1716-1717 (200...

Designing Si/porous-C composite with buffering voids as high capacity anode for lithium-ion batteries

International Nuclear Information System (INIS)

Yue, Lu; Zhang, Wenhui; Yang, Jingfeng; Zhang, Lingzhi

2014-01-01

A novel Si/porous-C composite with buffering voids was prepared by the co-assembly of phenol-formaldehyde resin, SiO 2 and Si nanoparticles, followed by a carbonizing process and subsequent removal of SiO 2 template. Si nanoparticle was coated with a layer of porous carbon shell with rationally designed void in between which provides the accommodating space for the volume change of Si over cycling. The as-prepared composite electrode exhibited good electrochemical performances as an anode material in lithium-ion cells, showing a stable reversible capacity of 980 mAh g −1 over 80 cycles with small capacity fade of 0.17%/cycle and high rate capability (721 mAh g −1 at 2000 mA g −1 )

Structural and compositional characterization of X-cut LiNbO3 crystals implanted with high energy oxygen and carbon ions

International Nuclear Information System (INIS)

Bentini, G.G.; Bianconi, M.; Cerutti, A.; Chiarini, M.; Pennestri, G.; Sada, C.; Argiolas, N.; Bazzan, M.; Mazzoldi, P.; Guzzi, R.

2005-01-01

High energy implantation of medium-light elements such as oxygen and carbon was performed in X-cut LiNbO 3 single crystals in order to prepare high quality optical waveguides. The compositional and damage profiles, obtained by exploiting the secondary ion mass spectrometry and Rutherford back-scattering techniques respectively, were correlated to the structural properties measured by the high resolution X-ray diffraction. This study evidences the development of tensile strain induced by the ion implantation that can contribute to the decrease of the ordinary refractive index variation through the photo-elastic effect

Detailed high-resolution three-dimensional simulations of OMEGA separated reactants inertial confinement fusion experiments

Energy Technology Data Exchange (ETDEWEB)

Haines, Brian M., E-mail: bmhaines@lanl.gov; Fincke, James R.; Shah, Rahul C.; Boswell, Melissa; Fowler, Malcolm M.; Gore, Robert A.; Hayes-Sterbenz, Anna C.; Jungman, Gerard; Klein, Andreas; Rundberg, Robert S.; Steinkamp, Michael J.; Wilhelmy, Jerry B. [Los Alamos National Laboratory, MS T087, Los Alamos, New Mexico 87545 (United States); Grim, Gary P. [Lawrence Livermore National Laboratory, Livermore, California 94550 (United States); Forrest, Chad J.; Silverstein, Kevin; Marshall, Frederic J. [Laboratory for Laser Energetics, University of Rochester, Rochester, New York 14623 (United States)

2016-07-15

We present results from the comparison of high-resolution three-dimensional (3D) simulations with data from the implosions of inertial confinement fusion capsules with separated reactants performed on the OMEGA laser facility. Each capsule, referred to as a “CD Mixcap,” is filled with tritium and has a polystyrene (CH) shell with a deuterated polystyrene (CD) layer whose burial depth is varied. In these implosions, fusion reactions between deuterium and tritium ions can occur only in the presence of atomic mix between the gas fill and shell material. The simulations feature accurate models for all known experimental asymmetries and do not employ any adjustable parameters to improve agreement with experimental data. Simulations are performed with the RAGE radiation-hydrodynamics code using an Implicit Large Eddy Simulation (ILES) strategy for the hydrodynamics. We obtain good agreement with the experimental data, including the DT/TT neutron yield ratios used to diagnose mix, for all burial depths of the deuterated shell layer. Additionally, simulations demonstrate good agreement with converged simulations employing explicit models for plasma diffusion and viscosity, suggesting that the implicit sub-grid model used in ILES is sufficient to model these processes in these experiments. In our simulations, mixing is driven by short-wavelength asymmetries and longer-wavelength features are responsible for developing flows that transport mixed material towards the center of the hot spot. Mix material transported by this process is responsible for most of the mix (DT) yield even for the capsule with a CD layer adjacent to the tritium fuel. Consistent with our previous results, mix does not play a significant role in TT neutron yield degradation; instead, this is dominated by the displacement of fuel from the center of the implosion due to the development of turbulent instabilities seeded by long-wavelength asymmetries. Through these processes, the long

Polymer-derived Ceramic SiCN-MoS2 Nanosheet Composite for Lithium Ion Battery Anodes

Science.gov (United States)

Bhandavat, Romil; Singh, Gurpreet

2012-02-01

We demonstrate synthesis of a novel SiCN-MoS2 nanosheet composite for use as Li-ion battery anode for high power applications. The nanosheet composite was prepared by thermal decomposition of polysilazane (SiCN precursor) on exfoliated MoS2 surfaces. The morphology and chemical structure was studied using a range of spectroscopy techniques that revealed a sidewall functionalization of exfoliated MoS2 by the polymeric precursor. The thermodynamic stability of SiCN-MoS2 nanosheets was also confirmed by thermo-gravimetric analysis (1000 degree C). Batteries assembled using MoS2-SiCN nanosheets as active anode material showed that lithium can be reversibly intercalated in the voltage range of 0-2.5 V with first cycle discharge capacity of 620 mAh/g at a current density of 100 mA/g.

Gamma-induced radiation polymerization of kaolin composite for sorption of lanthanum, europium and uranium ions from low-grade monazite leachate

International Nuclear Information System (INIS)

Metwally, S.S.; Hassan, R.S.; El-Masry, E.H.; Borai, E.H.

2018-01-01

Gamma radiation polymerization method was used for the modification of kaolin to produce (poly acrylamide-acrylic acid)-Kaolin (PAM-AA-K). Monazite ore is one of the main resources of uranium and lanthanide elements, therefore, this work focused on sorption of uranium, lanthanum and europium ions from low grade monazite leachate. The removal percent for Eu 3+ , La 3+ and UO 2 2+ are 94.6, 91.6 and 73.4%, respectively. Monolayer capacity of Eu 3+ , La 3+ and UO 2 2+ were found to be 54.64, 45.87 and 37.59 mg/g, respectively. The sorption mechanism of lanthanum and europium ions on PAM-AA-K composite mainly takes place as Ln(OH) 2+ , and for uranium as uranyl ion, UO 2 2+ . (author)

Preparation of fiber reinforced titanium diboride and boron carbide composite bodies

International Nuclear Information System (INIS)

Newkirk, L.R.; Riley, R.E.; Sheinberg, H.; Valencia, F.A.; Wallace, T.C.

1979-01-01

A process is described for uniformly infiltrating woven carbon cloth with either titanium diboride or boron carbide at reduced pressure (15 to 25 torr). The effects of deposition temperature on the uniformity of penetration and on coating rate are described for temperatures from 750 to 1000 0 C and deposit loadings from 20 to 43 vol. %. For the boron carbides, boron composition is discussed and evidence is presented suggesting that propene is the dominant rate controlling reactant

A novel and efficient water-based composite binder for LiCoO{sub 2} cathodes in lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Chu, Yung-Ju [Department of Materials and Mineral Resources Engineering, National Taipei University of Technology, Taipei (China); Peng, Xing-Wei [Institute of Materials Science and Engineering, National Taipei University of Technology, Taipei (China); Wang, Fu-Ming; Yang, Chang-Rung [Material and Chemical Research Laboratories, Industrial Technology Research Institute, Chutung, Hsinchu (China); Li, Chia-Chen [Department of Materials and Mineral Resources Engineering, National Taipei University of Technology, Taipei (China); Institute of Materials Science and Engineering, National Taipei University of Technology, Taipei (China); Lee, Jyh-Tsung

2007-11-15

The dispersion, adhesion strength, electrical, and electrochemical properties of LiCoO{sub 2} cathodes in lithium-ion batteries with the addition of a new composite binder composed of two acrylic emulsions, poly(butyl acrylate)-based (PBA) and polyacrylonitrile-based (PA) latex in a ratio of 3:7, were evaluated. PBA binder has a low-glass transition temperature of 10 C, which can improve the flexibility of the electrode. This new composite binder has a very good binding ability as same as the typical organic solvent-based binder, poly(vinylidene fluoride). The dispersions of the water-based cathode slurries with the composite binder were measured by analyzing the viscosity and sedimentation behaviors. The results show that the new composite binder can well disperse the LiCoO{sub 2}. Moreover, using the new composite binder could greatly improve the rate capabilities and the cycle stability of water-based LiCoO{sub 2} cathodes. (author)

Copper Ferrocyanide Functionalized Core-Shell Magnetic Silica Composites for the Selective Removal of Cesium Ions from Radioactive Liquid Waste.

Science.gov (United States)

Lee, Hyun Kyu; Yang, Da Som; Oh, Wonzin; Choi, Sang-June

2016-06-01

The copper ferrocyanide functionalized core-shell magnetic silica composite (mag@silica-CuFC) was prepared and was found to be easily separated from aqueous solutions by using magnetic field. The synthesized mag@silica-CuFC composite has a high sorption ability of Cs owing to its strong affinity for Cs as well as the high surface area of the supports. Cs sorption on the mag@silica-CuFC composite quickly reached the sorption equilibrium after 2 h of contact time. The effect of the presence of salts with a high concentration of up to 3.5 wt% on the efficiency of Cs sorption onto the composites was also studied. The maximum sorption ability was found to be maintained in the presence of up to 3.5 wt% of NaCl in the solution. Considering these results, the mag@silica-CuFC composite has great potential for use as an effective sorbent for the selective removal of radioactive Cs ions.

Electrochemical performance of SnO{sub 2}/modified graphite composite material as anode of lithium ion battery

Energy Technology Data Exchange (ETDEWEB)

Wang, Hong-Qiang [Guangxi Key Laboratory of Low Carbon Energy Materials, School of Chemical and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004 (China); Hubei Key Laboratory for Processing and Application of Catalytic Materials, Huanggang Normal University, Huanggang 438000 (China); Yang, Guan-Hua; Huang, You-Guo; Zhang, Xiao-Hui; Yan, Zhi-Xiong [Guangxi Key Laboratory of Low Carbon Energy Materials, School of Chemical and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004 (China); Li, Qing-Yu, E-mail: liqingyu62@126.com [Guangxi Key Laboratory of Low Carbon Energy Materials, School of Chemical and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004 (China)

2015-11-01

In this report, we synthesized SnO{sub 2}/modified graphite anode composite material by a simple reflux method using SnCl{sub 4}·5H{sub 2}O as tin source and modified graphite as carbon source. The as-obtained composite was investigated with the help of X-ray diffraction (XRD), scanning electron microscopy (SEM) and galvanostatic cycling tests. The results show that the composite has a wave-shaped fold structure and the SnO{sub 2} nanoparticles on it have an average size of about 50 nm. Compared to pure modified graphite, the SnO{sub 2}/modified graphite exhibits a better electrochemical performance with a reversible specific capacity of 581.7 mAh g{sup −1} after 80 cycles, owing to high mechanical stress and elasticity of modified graphite could hinder the volume effect of SnO{sub 2} nanoparticles during the Li{sup +} insertion/extraction process. All these favourable characters reveal that the composite is a great potential anode material in high-performance lithium ion batteries. - Highlights: • A simple synthetic method of SnO{sub 2}/modified graphite composite as anode. • The as-prepared composite with layered structure alleviates the huge reunion of SnO{sub 2}. • The composite exhibits a good capacity retention rate of 85.8% after 25 cycles.

Ion-induced surface modification of alloys

International Nuclear Information System (INIS)

Wiedersich, H.

1983-11-01

In addition to the accumulation of the implanted species, a considerable number of processes can affect the composition of an alloy in the surface region during ion bombardment. Collisions of energetic ions with atoms of the alloy induce local rearrangement of atoms by displacements, replacement sequences and by spontaneous migration and recombination of defects within cascades. Point defects form clusters, voids, dislocation loops and networks. Preferential sputtering of elements changes the composition of the surface. At temperatures sufficient for thermal migration of point defects, radiation-enhanced diffusion promotes alloy component redistribution within and beyond the damage layer. Fluxes of interstitials and vacancies toward the surface and into the interior of the target induce fluxes of alloying elements leading to depth-dependent compositional changes. Moreover, Gibbsian surface segregation may affect the preferential loss of alloy components by sputtering when the kinetics of equilibration of the surface composition becomes competitive with the sputtering rate. Temperature, time, current density and ion energy can be used to influence the individual processes contributing to compositional changes and, thus, produce a rich variety of composition profiles near surfaces. 42 references

Hierarchical structured graphene/metal oxide/porous carbon composites as anode materials for lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Guo, Rong [Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University, Beijing 100875 (China); Yue, Wenbo, E-mail: wbyue@bnu.edu.cn [Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University, Beijing 100875 (China); Ren, Yu [National Institute of Clean-and-Low-Carbon Energy, Beijing 102209 (China); Zhou, Wuzong [School of Chemistry, University of St. Andrews, St. Andrews, Fite KY16 9ST (United Kingdom)

2016-01-15

Highlights: • CeO{sub 2} and Co{sub 3}O{sub 4} nanoparticles display different behavior within CMK-3. • CMK-3-CeO{sub 2} and Co{sub 3}O{sub 4} show various electrochemical properties • CMK-3-CeO{sub 2} and Co{sub 3}O{sub 4} are further wrapped by graphene nanosheets. • Graphene-encapsulated composites show better electrochemical performances. - Abstract: As a novel anode material for lithium-ion batteries, CeO{sub 2} displays imperceptible volumetric and morphological changes during the lithium insertion and extraction processes, and thereby exhibits good cycling stability. However, the low theoretical capacity and poor electronic conductivity of CeO{sub 2} hinder its practical application. In contrast, Co{sub 3}O{sub 4} possesses high theoretical capacity, but undergoes huge volume change during cycling. To overcome these issues, CeO{sub 2} and Co{sub 3}O{sub 4} nanoparticles are formed inside the pores of CMK-3 and display various electrochemical behaviors due to the different morphological structures of CeO{sub 2} and Co{sub 3}O{sub 4} within CMK-3. Moreover, the graphene/metal oxide/CMK-3 composites with a hierarchical structure are then prepared and exhibit better electrochemical performances than metal oxides with or without CMK-3. This novel synthesis strategy is hopefully employed in the electrode materials design for Li-ion batteries or other energy conversion and storage devices.

Evaluation of capacity ion exchange of MMT-Na+with rare earth salts for use in polymeric nano composites

International Nuclear Information System (INIS)

Maino, Isabel B.; Scienza, Lisete C.; Piazza, Diego; Zattera, Ademir J.; Ferreira, Carlos A.

2011-01-01

The modification of the montmorillonite clay is associated with materials science, arousing interest in science and technology provide significant improvements when incorporated into polymeric materials neat and conventional composites. The process of modification of clays occurs mainly through the ion exchange of exchangeable cations in its crystal structure. In this study, we performed ion exchange of sodium montmorillonite with rare earth salts (cerium) through two routes: centrifugation and filtration. The samples were characterized by X-ray diffraction (XRD) and energy dispersive analysis by X-ray (EDS). The sample obtained by the filtration route showed an increase of basal clay by XRD, indicating the presence of salts of cerium on the structure, and corroborated by EDS analysis. (author)

Yolk-shell structured composite for fast and selective lithium ion sieving.

Science.gov (United States)

Li, Na; Lu, Deli; Zhang, Jinlong; Wang, Lingzhi

2018-06-15

Yolk-shell structured C@Li 4 Ti 5 O 12 microspheres composed of carbon core (ca. 500 nm) and sea urchin-like Li 4 Ti 5 O 12 shell (ca. 400-500 nm) are formed by hydrothermally treating the core-shell structured C@TiO 2 in the EtOH/H 2 O solution of LiOH and calcining it in N 2 atmosphere. Yolk-shell structured TiO 2 -type lithium ion sieve is further transformed from C@Li 4 Ti 5 O 12 through the acid treatment, which have a high specific surface area of 201.74 m 2 /g. The composite shows adsorption capacity towards Li + proportional to the pH value in the range of 7-13. The adsorption reaches equilibrium within 2 h with a high equilibrium adsorption capacity of 28.46 mg/g under alkaline conditions, which is ca. 8 times the value of ordinary TiO 2 lithium ion sieve with comparable size and surface area, demonstrating the enhanced adsorption is attributed to the generation of more accessible surficial voids by replacing internal part with light carbon core. The adsorption follows Freundlich and pseudo-second-order kinetic models with a high rate constant of 0.015 g/(mg·min). The selective adsorption to Li + is verified in the presence of K + , Na + , Ca 2+ and Mg 2+ . Copyright © 2018 Elsevier Inc. All rights reserved.

High performance Li2MnO3/rGO composite cathode for lithium ion batteries

Science.gov (United States)

Zhao, Wei; Xiong, Lilong; Xu, Youlong; Li, Houli; Ren, Zaihuang

2017-05-01

The novel composite Li2MnO3 (LMO)/reduced graphene oxide (rGO) has been synthesized successfully. Based on the scanning electron microscopy and transmission electron microscopy, LMO is found to distribute separately on the rGO sheets by forming a laminated structure, which is in favor of good electrical contact between the cathode active materials and the rGO matrix, and also facilitates the separation of LMO secondary particles with reduced size. Cyclic voltammetry and electrochemical impedance spectroscopy tests show that the charge transfer resistance decreases from 81.2 Ω for LMO to 29.6 Ω for LMO/rGO composite. The Li-ion diffusion coefficient of LMO/rGO composite is almost triple that of LMO. As a result, the LMO/rGO composite delivers an initial discharge capacity of 284.9 mAh g-1 with a capacity retention of 86.6% after 45 cycles at 0.1 C between 2.0 and 4.6 V. Cycle performance is even better at a higher current density 0.2 C while the retention ratio is up to 97.1% after 45 cycles. The rate capability is also significantly enhanced, and the LMO/rGO composite could exhibit a large discharge capacity of 123.7 mAh g-1 which is more than three times larger than that of LMO (40.8 mAh g-1) at a high rate of 8 C.

SiOx/C composite from rice husks as an anode material for lithium-ion batteries

International Nuclear Information System (INIS)

Ju, Yanming; Tang, Joel A.; Zhu, Kai; Meng, Yuan; Wang, Chunzhong; Chen, Gang; Wei, Yingjin; Gao, Yu

2016-01-01

Highlights: • Rice husks were utilized to prepare SiO x /C as an anode material for lithium ion battery. • SiO x /C composite was prepared by a two-step fire process. • SiO x /C contains low valence silicon owing to thermal treatment at argon/hydrogen atmosphere. • SiO x /C exhibits a high specific capacity of nearly 600 mAh g −1 at 100 mA g −1 current density after 100 cycles. - Abstract: SiO x /C composite material derived directly from agricultural rice husk byproducts through an economically viable and environmentally benign approach has been explored to be used as an anode for rechargeable lithium batteries. Rice husks were converted into a SiO x /C composite directly by heat treatment under argon/hydrogen atmosphere, at a temperature of 900 °C. The composite contains SiO x surrounded by an amorphous carbon matrix. A steady state reversible capacity of nearly 600 mAh g −1 was delivered at 100 mA g −1 current density after 100 cycles. The improved performance of the SiO x /C composite anode over other agricultural byproduct derived carbon materials is believed to be due to the presence of low valence silicon. The filth-to-wealth conversion of rice husks to battery material is a highly energy efficient process with great economic and environmental benefits.

Source Regions of the Interplanetary Magnetic Field and Variability in Heavy-Ion Elemental Composition in Gradual Solar Energetic Particle Events

Science.gov (United States)

Ko, Yuan-Kuen; Tylka, Allan J.; Ng, Chee K.; Wang, Yi-Ming; Dietrich, William F.

2013-01-01

Gradual solar energetic particle (SEP) events are those in which ions are accelerated to their observed energies by interactions with a shock driven by a fast coronal mass-ejection (CME). Previous studies have shown that much of the observed event-to-event variability can be understood in terms of shock speed and evolution in the shock-normal angle. But an equally important factor, particularly for the elemental composition, is the origin of the suprathermal seed particles upon which the shock acts. To tackle this issue, we (1) use observed solar-wind speed, magnetograms, and the PFSS model to map the Sun-L1 interplanetary magnetic field (IMF) line back to its source region on the Sun at the time of the SEP observations; and (2) then look for correlation between SEP composition (as measured by Wind and ACE at approx. 2-30 MeV/nucleon) and characteristics of the identified IMF-source regions. The study is based on 24 SEP events, identified as a statistically-significant increase in approx. 20 MeV protons and occurring in 1998 and 2003-2006, when the rate of newly-emergent solar magnetic flux and CMEs was lower than in solar-maximum years and the field-line tracing is therefore more likely to be successful. We find that the gradual SEP Fe/O is correlated with the field strength at the IMF-source, with the largest enhancements occurring when the footpoint field is strong, due to the nearby presence of an active region. In these cases, other elemental ratios show a strong charge-to-mass (q/M) ordering, at least on average, similar to that found in impulsive events. These results lead us to suggest that magnetic reconnection in footpoint regions near active regions bias the heavy-ion composition of suprathermal seed ions by processes qualitatively similar to those that produce larger heavy-ion enhancements in impulsive SEP events. To address potential technical concerns about our analysis, we also discuss efforts to exclude impulsive SEP events from our event sample.

Preparation and electrochemical properties of nanocable-like Nb2O5/surface-modified carbon nanotubes composites for anode materials in lithium ion batteries

International Nuclear Information System (INIS)

Shi, Chongfu; Xiang, Kaixiong; Zhu, Yirong; Chen, Xianhong; Zhou, Wei; Chen, Han

2017-01-01

Highlights: •The acid pretreatment for CNTs is a key factor to fabricate nanocable-like Nb 2 O 5 /SMCNTs composites. •The polar functional groups can induce the symmetrical growth of Nb 2 O 5 nanoparticitles on the surface of SMCNTs. •SMCNTs can provide sufficient conductive contacts for composites and abundant active sites for electrochemical reaction. -- Abstract: Uniform nanocable-like Nb 2 O 5 /surface-modified carbon nanotubes (SMCNTs) composites for anode materials in lithium ion batteries were synthesized by hydrothermal method. It was indicated that Nb 2 O 5 nanoparticles were tightly and uniformly cultivated on carbon nanotubes when CNTs were pretreated with concentrated H 2 SO 4 . As a result, Nb 2 O 5 /SMCNTs composite materials showed remarkable electrochemical performance as anode materials for lithium-ion batteries. It delivered a high reversible capacity of 441 mA h g −1 cycled at the current density of 40 mA g −1 after 100 cycles and an excellent rate capacity of 185 mA h g −1 at the high current density of 5000 mA g −1 after 200 cycles.

Development of industrial ion implantation and ion assisted coating processes: A perspective

International Nuclear Information System (INIS)

Legg, K.O.; Solnick-Legg, H.

1989-01-01

Ion beam processes have gone through a series of developmental stages, from being the mainstay of the semiconductor industry for production of integrated circuits, to new commercial processes for biomedical, aerospace and other industries. Although research is still continuing on surface modification using ion beam methods, ion implantation and ion assisted coatings for treatment of metals, ceramics, polymers and composites must now be considered viable industrial processes of benefit in a wide variety of applications. However, ion implantation methods face various barriers to acceptability, in terms not only of other surface treatment processes, but for implantation itself. This paper will discuss some of the challenges faced by a small company whose primary business is development and marketing of ion implantation and ion-assisted coating processes. (orig.)

Determination of feedstuff amino acids composition by ion-exchange chromatography

Directory of Open Access Journals (Sweden)

A. A. Volnin

2018-01-01

Full Text Available Determination of animal feeds amino acids composition is the very important part of agricultural sciences and livestock management. This is necessary for normalization and balanced of farm animal’s diets parameters. Advances in husbandry techniques are making in response to the needs for rearing high genetic merit livestock. The nutrition of livestock has a critical role in these developments and is an element which needs to be continually updated as new scientific information becomes available. This article is devoted to the use of ion-exchange chromatography with post-colum derivatization by ninhydrin in the study of the amino acid composition and evaluation of the biological value of livestock feedstuff components. The amino acid composition (except tryptophan of the livestock feed-stuff component is presented for threonine – 3.26 g/100g of protein, leucine – 6.43, isoleucine – 3.24, valine – 4.77, methionine – 2.18, lysine – 2.90, phenylalanine – 3.16, histidine – 2.03, tyrosine – 2.33, sum of asparagine and aspartate – 6.76, serine – 3.97, sum of glutamine and glutamic acid – 12.04, glycine – 6.00, alanine – 6.71, arginine – 6.93, proline – 3.08, sum of cystine and cysteine – 1.38. Biological value of feedstuff component compared with the "ideal" protein (FAO WHO is estimated, limiting amino acids were found. The amino acid score was calculated: for threonine – 81.5%, leucine – 91.9%, isoleucine – 81%, valine – 95.4%, lysine – 52.7%, phenylalanine and tyrosine sum – 91.5%, methionine and cysteine sum – 101.7%. Feedstuff component had a low level of essential amino acids in compare with "ideal" protein (FAO WHO. Feedstuff component can be used for livestock nutrition as a component of essential amino-acid balanced diet.

Development of composite ion exchanger for separation of cesium from high level liquid waste

International Nuclear Information System (INIS)

Kumar, A.; Varshney, L.

2010-01-01

137 Cs (t 1/2 = 30 years) is one of the major radioisotope present in high level liquid waste (HLLW) generated during the reprocessing of nuclear fuel. Separation of 137 Cs from HLLW results in reduction of personal radiation exposure during the conditioning, transportation, storage and disposal. In addition, 137 Cs has enormous application as a radiation source in food preservation, sterilization of medical products, brachytherapy, blood irradiation, hygienization of sewage sludge etc. Ammonium molybdophosphate (AMP), an inorganic ion exchanger, has high selectivity and high exchange capacity for Cs. It exits as microcrystalline powder which is not amenable for column operation. ALIX is a composite material in which AMP is physically blended with inert polymeric substrate to improve its column property, exchange kinetics and increase its mechanical strength. The observed excellent properties of the composite are attributed to its engineered structure which is formed during its production. SEM analysis of ALIX shows that AMP crystals embedded in the cavities are not covered by the polymer which greatly enhances its availability for cesium exchange. The highly porous structure of the composite having 49% void volume facilitates faster kinetics of exchange of Cs from the aqueous phase and increased rate of reaction with alkali required during its dissolution

Facile synthesis and stable cycling ability of hollow submicron silicon oxide–carbon composite anode material for Li-ion battery

Energy Technology Data Exchange (ETDEWEB)

Kim, Joong-Yeon; Nguyen, Dan Thien [Department of Fine Chemical Engineering & Applied Chemistry, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Kang, Joon-Sup [Department of Energy Science and Technology, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Song, Seung-Wan, E-mail: swsong@cnu.ac.kr [Department of Fine Chemical Engineering & Applied Chemistry, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Department of Energy Science and Technology, Chungnam National University, Daejeon 305-764 (Korea, Republic of)

2015-06-05

Highlights: • Hollow submicron SiO{sub 2}–carbon composite material was synthesized using Si{sup 4+}-citrate chelation. • Composite material possessed a homogeneous distribution of SiO{sub 2} and carbon. • Composite electrode delivered ⩾600 mAh/g with a stable cycling stability. • This materials design and synthesis provides a useful platform for scalable production. - Abstract: Advanced SiO{sub 2}–carbon composite anode active material for lithium-ion battery has been synthesized through a simple chelation of silicon cation with citrate in a glyme-based solvent. The resultant composite material demonstrates a homogeneous distribution of constituents over the submicron particles and a unique hollow spherical microstructure, which provides an enhanced electrical conductivity and better accommodation of volume change of silicon during electrochemical charge–discharge cycling, respectively. As a result, the composite electrode exhibits a high cycling stability delivering the capacity retention of 91% at the 100th cycle and discharge capacities of 662–602 mAh/g and coulombic efficiencies of 99.8%. This material synthesis is scalable and cost-effective in preparing various submicron or micron composite electrode materials.

Silicon Composite Anode Materials for Lithium Ion Batteries Based on Carbon Cryogels and Carbon Paper

Science.gov (United States)

Woodworth, James; Baldwin, Richard; Bennett, William

2010-01-01

A variety of materials are under investigation for use as anode materials in lithium-ion batteries, of which, the most promising are those containing silicon. One such material is a composite formed via the dispersion of silicon in a resorcinol-formaldehyde (RF) gel followed by pyrolysis. Two silicon-carbon composite materials, carbon microspheres and nanofoams produced from nano-phase silicon impregnated RF gel precursors have been synthesized and investigated. Carbon microspheres are produced by forming the silicon-containing RF gel into microspheres whereas carbon nanofoams are produced by impregnating carbon fiber paper with the silicon containing RF gel to create a free standing electrode. Both materials have demonstrated their ability to function as anodes and utilize the silicon present in the material. Stable reversible capacities above 400 mAh/g for the bulk material and above 1000 mAh/g of Si have been observed.

Facile and large-scale preparation of sandwich-structured graphene-metal oxide composites as anode materials for Li-ion batteries

International Nuclear Information System (INIS)

Fang, Hongmei; Zhao, Li; Yue, Wenbo; Wang, Yuan; Jiang, Yang; Zhang, Yuan

2015-01-01

Graphene-based metal oxides are desirable as potential anode materials for lithium-ion batteries (LIBs) owing to their superior electrochemical properties. In this work, sandwich-structured graphene-metal oxide (ZnO, NiO) composites are facilely synthesized on a large scale through self-assembly of graphene oxide nanosheets and metal ammine complexes, and then thermal decomposition of the self-assembled products. ZnO or NiO nanoparticles with diameters of 5∼10 nm are immobilized between the layers of graphene nanosheets, which may provide the space for accommodating the volume change of metal oxides during cycles, and highly improve the electronic conductivity of the composites. Accordingly, these sandwich-structured composites exhibit enhanced electrochemical performances compared to metal oxide particles or stacked graphene nanosheets. This facile synthesis method is very suitable for the large-scale production of three-dimensional graphene-based composites as high-performance anodes for LIBs.

A New Class of Ternary Compound for Lithium-Ion Battery: from Composite to Solid Solution.

Science.gov (United States)

Wang, Jiali; Wu, Hailong; Cui, Yanhua; Liu, Shengzhou; Tian, Xiaoqing; Cui, Yixiu; Liu, Xiaojiang; Yang, Yin

2018-02-14

Searching for high-performance cathode materials is a crucial task to develop advanced lithium-ion batteries (LIBs) with high-energy densities for electrical vehicles (EVs). As a promising lithium-rich material, Li 2 MnO 3 delivers high capacity over 200 mAh g -1 but suffers from poor structural stability and electronic conductivity. Replacing Mn 4+ ions by relatively larger Sn 4+ ions is regarded as a possible strategy to improve structural stability and thus cycling performance of Li 2 MnO 3 material. However, large difference in ionic radii of Mn 4+ and Sn 4+ ions leads to phase separation of Li 2 MnO 3 and Li 2 SnO 3 during high-temperature synthesis. To prepare solid-solution phase of Li 2 MnO 3 -Li 2 SnO 3 , a buffer agent of Ru 4+ , whose ionic radius is in between that of Mn 4+ and Sn 4+ ions, is introduced to assist the formation of a single solid-solution phase. The results show that the Li 2 RuO 3 -Li 2 MnO 3 -Li 2 SnO 3 ternary system evolves from mixed composite phases into a single solid-solution phase with increasing Ru content. Meanwhile, discharge capacity of this ternary system shows significantly increase at the transformation point which is ascribed to the improvement of Li + /e - transportation kinetics and anionic redox chemistry for solid-solution phase. The role of Mn/Sn molar ratio of Li 2 RuO 3 -Li 2 MnO 3 -Li 2 SnO 3 ternary system has also been studied. It is revealed that higher Sn content benefits cycling stability of the system because Sn 4+ ions with larger sizes could partially block the migration of Mn 4+ and Ru 4+ from transition metal layer to Li layer, thus suppressing structural transformation of the system from layered-to-spinel phase. These findings may enable a new route for exploring ternary or even quaternary lithium-rich cathode materials for LIBs.

Compositionally graded SiCu thin film anode by magnetron sputtering for lithium ion battery

Energy Technology Data Exchange (ETDEWEB)

Polat, B.D., E-mail: bpolat@itu.edu.tr [Department of Metallurgical and Materials Engineering, Istanbul Technical University, Maslak, Istanbul 34469 (Turkey); Eryilmaz, O.L. [Energy Systems Division, Argonne National Laboratory, Argonne, IL 60439 (United States); Keleş, O., E-mail: ozgulkeles@itu.edu.tr [Department of Metallurgical and Materials Engineering, Istanbul Technical University, Maslak, Istanbul 34469 (Turkey); Erdemir, A. [Energy Systems Division, Argonne National Laboratory, Argonne, IL 60439 (United States); Amine, K. [Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, IL 60439 (United States)

2015-12-01

Compositionally graded and non-graded composite SiCu thin films were deposited by magnetron sputtering technique on Cu disks for investigation of their potentials in lithium ion battery applications. The compositionally graded thin film electrodes with 30 at.% Cu delivered a 1400 mAh g{sup −1} capacity with 80% Coulombic efficiency in the first cycle and still retained its capacity at around 600 mAh g{sup −1} (with 99.9% Coulombic efficiency) even after 100 cycles. On the other hand, the non-graded thin film electrodes with 30 at.% Cu exhibited 1100 mAh g{sup −1} as the first discharge capacity with 78% Coulombic efficiency but the cycle life of this film degraded very quickly, delivering only 250 mAh g{sup −1} capacity after 100th cycles. Not only the Cu content but also the graded film thickness were believed to be the main contributors to the much superior performance of the compositionally graded SiCu films. We also believe that the Cu-rich region of the graded film helped reduce internal stress build-up and thus prevented film delamination during cycling. In particular, the decrease of Cu content from interface region to the top of the coating reduced the possibility of stress build-up across the film during cycling, thus leading to a high electrochemical performance.b - Highlights: • Highly adherent SiCu films are deposited by magnetron sputtering. • Compositionally graded SiCu film is produced and characterized. • Decrease of Cu content diverted the propagation of stress in the anode. • Cu rich layer at the bottom improves the adherence of the film.

Redox flow batteries with serpentine flow fields: Distributions of electrolyte flow reactant penetration into the porous carbon electrodes and effects on performance

Science.gov (United States)

Ke, Xinyou; Prahl, Joseph M.; Alexander, J. Iwan D.; Savinell, Robert F.

2018-04-01

Redox flow batteries with flow field designs have been demonstrated to boost their capacities to deliver high current density and power density in medium and large-scale energy storage applications. Nevertheless, the fundamental mechanisms involved with improved current density in flow batteries with serpentine flow field designs have been not fully understood. Here we report a three-dimensional model of a serpentine flow field over a porous carbon electrode to examine the distributions of pressure driven electrolyte flow penetrations into the porous carbon electrodes. We also estimate the maximum current densities associated with stoichiometric availability of electrolyte reactant flow penetrations through the porous carbon electrodes. The results predict reasonably well observed experimental data without using any adjustable parameters. This fundamental work on electrolyte flow distributions of limiting reactant availability will contribute to a better understanding of limits on electrochemical performance in flow batteries with serpentine flow field designs and should be helpful to optimizing flow batteries.

Layered rare-earth hydroxide (LRH, R = Tb, Y) composites with fluorescein: delamination, tunable luminescence and application in chemosensoring for detecting Fe(iii) ions.

Science.gov (United States)

Su, Feifei; Guo, Rong; Yu, Zihuan; Li, Jian; Liang, Zupei; Shi, Keren; Ma, Shulan; Sun, Genban; Li, Huifeng

2018-04-17

We demonstrate a novel example of tunable luminescence and the application of the delaminated FLN/OS-LRH composites (LRHs are layered rare-earth hydroxides, R = Tb, Y; FLN is the fluorescein named 2-(6-hydroxy-3-oxo-(3H)-xanthen-9-yl)benzoic acid; OS is the anionic surfactant 1-octane sulfonic acid sodium) in detecting Fe(iii) ions. The FLNxOS1-x species (x = 0.02, 0.05, 0.10, and 0.20) are intercalated into the LTbyY1-yH layers (y = 1, 0.9, 0.7, 0.5, 0.3, 0.1 and 0) by ion exchange reactions to yield the composites FLNxOS1-x-LTbyY1-yH. In the solid state, the LYH composites display green emission (564 nm) arising from the organic FLN, while in LTbH composites, the luminescence of the Tb3+ in the layers (545 nm) and the FLN in the interlayers is co-quenched. In the delaminated state in formamide (FM), FLNxOS1-x-LTbH composites display green to yellowish-green luminescence (540-574 nm) following the increasing FLN/OS ratio; while the FLN0.02OS0.98-LTbyY1-yH composites show green emission at ∼540 nm. The fluorescence lifetimes of the composites (4.22-4.63 ns) are comparable to the free FLN-Na, and the quantum yields (31.62-78.70%) of the composites especially that (78.70%) of the FLN0.02OS0.98-LYH are much higher than that (28.40%) of free FLN-Na. The recognition ability of the FLN0.02OS0.98-LYH composite for metal cations is researched. The delaminated FLN0.02OS0.98-LYH colloidal suspension exhibits high selectivity for Fe3+ over other ions (Mg2+, Al3+, Ni2+, Co2+, Cu2+, Zn2+, Mn2+, Pb2+, and Cd2+) with fluorescence quenching, which can work as a kind of turn-off fluorescence sensor for the detection of Fe3+. The detection limit of Fe3+ is determined to be 2.58 × 10-8 M and the quenching constant (Ksv) is 1.70 × 103 M-1. This is the first work on LRH materials working as a chemosensor for recognising metal cations. It provides a new approach for the design of LRH materials to be applied in fluorescence chemosensing.

Synthesis of Li2MnSiO4-graphene composite and its electrochemical performances as a cathode material for lithium ion batteries.

Science.gov (United States)

Kim, Jeonghyun; Song, Taeseup; Park, Hyunjung; Yuh, Junhan; Paik, Ungyu

2014-10-01

The Li2MnSiO4 is a promising candidate as a cathode for lithium ion batteries due to its large theoretical capacity of 330 mA h g(-1) and high thermal stability. However, the problems related to low electronic conductivity and large irreversible capacity at the first cycle limits its practical use as a Li-ion cathode material. We have developed a carbon coated Li2MnSiO4-graphene composite electrode to overcome these problems. Our designed electrode exhibits high reversible capacity of 301 mA h g(-1), with a high initial coulombic efficiency, and a discharge capacity at current rate of 0.5 C, that is double value of carbon coated Li2MnSiO4-carbon black composite electrode. These significant improvements are attributed to fast electron transport along the graphene sheet.

Replacing Chlorine with Hydrogen Chloride as a Possible Reactant for Synthesis of Titanium Carbide Derived Carbon Powders for High-Technology Devices

International Nuclear Information System (INIS)

Tallo, Indrek; Thomberg, Thomas; Jänes, Alar; Lust, Enn

2013-01-01

Micro- and mesoporous carbide-derived carbons were synthesized from titanium carbide (TiC) powder via gas phase reaction by using different reactants (Cl 2 and HCl) within the temperature range from 700 to 1100 °C. Analysis of XRD results show that TiC-derived carbons (TiC-CDC) consist mainly of graphitic crystallites. The first-order Raman spectra showed the graphite-like absorption peaks at ∼1577 cm 1 and the disorder-induced peaks at ∼1338 cm- 1 . The energy-related properties of supercapacitors based on 1 M (C 2 H 5 ) 3 CH 3 NBF 4 in acetonitrile and carbide-derived carbons (TiC-CDC (Cl 2 ) and TiC-CDC (HCl)) as electrode materials were also investigated using cyclic voltammetry, electrochemical impedance spectroscopy, galvanostatic charge/discharge and constant power methods. The Ragone plots for carbide-derived carbons prepared by using different reactants (Cl 2 , HCl) are quite similar and at high power loads TiC-CDC (Cl 2 ) material synthesized at 900 °C, i.e. materials with optimal porous structure, deliver higher power at constant energy

Hybrid lithium-ion capacitor with LiFePO4/AC composite cathode - Long term cycle life study, rate effect and charge sharing analysis

Science.gov (United States)

Shellikeri, A.; Yturriaga, S.; Zheng, J. S.; Cao, W.; Hagen, M.; Read, J. A.; Jow, T. R.; Zheng, J. P.

2018-07-01

Energy storage devices, which can combine the advantages of lithium-ion battery with that of electric double layer capacitor, are of prime interest. Recently, composite cathodes, which combine a battery material with capacitor material, have shown promise in enhancing life cycle and energy/power performances. Lithium-ion capacitor (LIC), with unique charge storage mechanism of combining a pre-lithiated battery anode with a capacitor cathode, is one such device which has the potential to synergistically incorporate the composite cathode to enhance capacity and cycle life. We report here a hybrid LIC consisting of a lithium iron phosphate (LiFePO4-LFP)/Activated Carbon composite cathode in combination with a hard carbon anode, by integrating the cycle life and capacity enhancing strategies of a dry method of electrode fabrication, anode pre-lithiation and a 3:1 anode to cathode capacity ratio, demonstrating a long cycle life, while elaborating on the charge sharing between the faradaic and non-faradaic mechanism in the battery and capacitor materials, respectively in the composite cathode. An excellent cell capacity retention of 94% (1000 cycles at 1C) and 92% (100,000 cycles at 60C) were demonstrated, while retaining 78% (over 6000 cycles at 2.7C) and 67% (over 70,000 cycles at 43C) of the LFP capacity in the composite cathode.

Preparation of Li_4Ti_5O_1_2 nanosheets/carbon nanotubes composites and application of anode materials for lithium-ion batteries

International Nuclear Information System (INIS)

Zhang, Pengfei; Chen, Ming; Shen, Xiao; Wu, Qianhui; Zhang, Xiue; Huan, Long; Diao, Guowang

2016-01-01

Highlights: • LTO NSs/CNTs composites are synthesized by a facile and scalable strategy. • The incorporation of CNTs into LTO NSs forms a delicate conductive network. • LTO NSs/CNTs composites display excellent rate and cycling performances. • LTO NSs/CNTs show low polarization and large diffusion coefficient of Li"+. - Abstract: Li_4Ti_5O_1_2 nanosheets (LTO NSs)/carbon nanotubes (CNTs) composites are synthesized using a facile, reproducible, and scalable strategy. In the hydrothermal process, the introduction of CNTs significantly improves the rate performance of LTO NSs. The incorporation of CNTs into the LTO NSs forms a delicate conductive network for rapid electron and lithium ions transport, resulting in excellent rate performance and superior cycling performance. LTO NSs/7.5%-CNTs composites show the highest reversible capacity and high-rate capability (a reversible capability of 157, 145, 132, 118, and 105 mA h g"−"1 at 1, 2, 3, 4, 5 A g"−"1, respectively) with good cycling performance (approximate 6.9% capacity loss after 1000 cycles at 2 A g"−"1 with a capacity retention of 135 mA h g"−"1), which is apparently larger than pristine LTO NSs. The significantly improved rate capability and cycling performance of the LTO NSs/CNTs composites are mainly attributed to their the lower polarization of potential difference, the larger diffusion coefficient of lithium ion and smaller charge-transfer resistance than pure LTO NSs.

First-Principles Study of MoO3/Graphene Composite as Cathode Material for High-Performance Lithium-Ion Batteries

Science.gov (United States)

Cui, Yanhua; Zhao, Yu; Chen, Hong; Wei, Kaiyuan; Ni, Shuang; Cui, Yixiu; Shi, Siqi

2018-03-01

Using first-principles calculations, we have systematically investigated the adsorption and diffusion behavior of Li in MoO3 bulk, on MoO3 (010) surface and in MoO3/graphene composite. Our results indicate that, in case of MoO3 bulk, Li diffusion barriers in the interlayer and intralayer spaces are 0.55 eV and 0.58 eV respectively, which are too high to warrant fast Lithium-ion charge/discharge processes. While on MoO3 (010) surface, Li exhibits a diffusion barrier as low as 0.07 eV which guarantees an extremely fast Li diffusion rate during charge/discharge cycling. However, in MoO3/graphene monolayer, Li diffusion barrier is at the same level as that on MoO3 (010) surface, which also ensures a very rapid Li charge/discharge rate. The rapid Li charge/discharge rate in this system originates from the removal of the upper dangling O1 atoms which hinder the Li diffusion on the lower MoO3 layer. Besides this, due to the interaction between Li and graphene, the Li average binding energy increases to 0.14 eV compared to its value on MoO3 (010) surface which contributes to a higher voltage. Additionally, the increased ratio of surface area provides more space for Li storage and the capacity of MoO3/graphene composite increases up to 279.2 mAhg-1. The last but not the least, due to the high conductivity of graphene, the conductivity of MoO3/graphene composite enhances greatly which is beneficial for electrode materials. In the light of present results, MoO3/graphene composite exhibits higher voltage, good conductivity, large Li capacity and very rapid Li charge/discharge rate, which prove it as a promising cathode material for high-performance lithium-ion batteries (LIBs).

Graphene oxide-multiwalled carbon nanotubes composite as an anode for lithium ion batteries

Directory of Open Access Journals (Sweden)

Majchrzycki Łukasz

2016-09-01

Full Text Available Nowadays reduced graphene oxide (rGO is regarded as a highly interesting material which is appropriate for possible applications in electrochemistry, especially in lithium-ion batteries (LIBs. Several methods were proposed for the preparation of rGO-based electrodes, resulting in high-capacity LIBs anodes. However, the mechanism of lithium storage in rGO and related materials is still not well understood. In this work we focused on the proposed mechanism of favorable bonding sites induced by additional functionalities attached to the graphene planes. This mechanism might increase the capacity of electrodes. In order to verify this hypothesis the composite of non-reduced graphene oxide (GO with multiwalled carbon nanotubes electrodes was fabricated. Electrochemical properties of GO composite anodes were studied in comparison with similarly prepared electrodes based on rGO. This allowed us to estimate the impact of functional groups on the reversible capacity changes. As a result, it was shown that oxygen containing functional groups of GO do not create, in noticeable way, additional active sites for the electrochemical reactions of lithium storage, contrary to what has been postulated previously.

Correlation of precursor and product ions in single-stage high resolution mass spectrometry. A tool for detecting diagnostic ions and improving the precursor elemental composition elucidation

Energy Technology Data Exchange (ETDEWEB)

Borràs, S. [Departament de Química Analítica, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Kaufmann, A., E-mail: anton.kaufmann@klzh.ch [Official Food Control Authority, Fehrenstrasse 15, 8032 Zürich (Switzerland); Companyó, R. [Departament de Química Analítica, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain)

2013-04-15

Highlights: ► We are describing a technique to spot ions which are derived from each other. ► Single stage high resolution data is used. ► This “in silicon” technique is compared to conventional precursor scan. ► Some applications for this technique are presented. -- Abstract: Monitoring of common diagnostic fragments is essential for recognizing molecules which are members of a particular compound class. Up to now, unit resolving tandem quadrupole mass spectrometers, operating in the precursor ion scan mode, have been typically used to perform such analysis. By means of high-resolution mass spectrometry (HRMS) a much more sensitive and selective detection can be achieved. However, using a single-stage HRMS instrument, there is no unequivocal link to the corresponding precursor ion, since such instrumentation does not permit a previous precursor selection. Thus, to address this limitation, an in silico approach to locate precursor ions, based on diagnostic fragments, was developed. Implemented as an Excel macro, the algorithm rapidly assembles and surveys exact mass data to provide a list of feasible precursor candidates according to the correlation of the chromatographic peak shape profile and other additional filtering criteria (e.g. neutral losses and isotopes). The macro was tested with two families of veterinary drugs, sulfonamides and penicillins, which are known to yield diagnostic product ions when fragmented. Data sets obtained from different food matrices (fish and liver), both at high and low concentration of the target compounds, were investigated in order to evaluate the capabilities and limitations of the reported approach. Finally, other possible applications of this technique, such as the elucidation of elemental compositions based on product ions and corresponding neutral losses, were also presented and discussed.

Correlation of precursor and product ions in single-stage high resolution mass spectrometry. A tool for detecting diagnostic ions and improving the precursor elemental composition elucidation

International Nuclear Information System (INIS)

Borràs, S.; Kaufmann, A.; Companyó, R.

2013-01-01

Highlights: ► We are describing a technique to spot ions which are derived from each other. ► Single stage high resolution data is used. ► This “in silicon” technique is compared to conventional precursor scan. ► Some applications for this technique are presented. -- Abstract: Monitoring of common diagnostic fragments is essential for recognizing molecules which are members of a particular compound class. Up to now, unit resolving tandem quadrupole mass spectrometers, operating in the precursor ion scan mode, have been typically used to perform such analysis. By means of high-resolution mass spectrometry (HRMS) a much more sensitive and selective detection can be achieved. However, using a single-stage HRMS instrument, there is no unequivocal link to the corresponding precursor ion, since such instrumentation does not permit a previous precursor selection. Thus, to address this limitation, an in silico approach to locate precursor ions, based on diagnostic fragments, was developed. Implemented as an Excel macro, the algorithm rapidly assembles and surveys exact mass data to provide a list of feasible precursor candidates according to the correlation of the chromatographic peak shape profile and other additional filtering criteria (e.g. neutral losses and isotopes). The macro was tested with two families of veterinary drugs, sulfonamides and penicillins, which are known to yield diagnostic product ions when fragmented. Data sets obtained from different food matrices (fish and liver), both at high and low concentration of the target compounds, were investigated in order to evaluate the capabilities and limitations of the reported approach. Finally, other possible applications of this technique, such as the elucidation of elemental compositions based on product ions and corresponding neutral losses, were also presented and discussed

A high current metal vapour vacuum arc ion source for ion implantation studies

International Nuclear Information System (INIS)

Evans, P.J.; Noorman, J.T.; Watt, G.C.; Cohen, D.D.; Bailey, G.M.

1989-01-01

The main features of the metal vapour vacuum arc(MEVA) as an ion source are presented. The technology utilizes the plasma production capabilities of a vacuum arc cathode. Some of the ions produced in this discharge flow through the anode and the 3 extraction grids to form an extracted ion beam. The high beam current and the potential for generating broad beams, make this technology suitable for implantation of large surface areas. The composition of the vacuum arc cathode determines the particular ions obtained from the MEVA source. 3 refs., 1 tab., 2 figs

Experimental investigation of a passive thermal management system for high-powered lithium ion batteries using nickel foam-paraffin composite

International Nuclear Information System (INIS)

Hussain, Abid; Tso, C.Y.; Chao, Christopher Y.H.

2016-01-01

It is necessary for electric vehicles (EVs) and hybrid electric vehicles (HEVs) to have a highly efficient thermal management system to maintain high powered lithium ion batteries within permissible temperature limits. In this study, an efficient thermal management system for high powered lithium ion batteries using a novel composite (nickel foam-paraffin wax) is designed and investigated experimentally. The results have been compared with two other cases: a natural air cooling mode and a cooling mode with pure phase change materials (PCM). The results indicate that the safety demands of lithium ion batteries cannot be fulfilled using natural air convection as the thermal management mode. The use of PCM can dramatically reduce the surface temperature within the permissible range due to heat absorption by the PCM undergoing phase change. This effect can be further enlarged by using the nickel foam-paraffin composite, showing a temperature reduction of 31% and 24% compared to natural air convection and pure PCM, respectively under 2 C discharge rate. The effect of the geometric parameters of the foam on the battery surface temperature has also been studied. The battery surface temperature decreases with the decrease of porosity and the pore density of the metal foam. On the other hand, the discharge capacity increases with the increase in porosity, but decreases with pore density. - Highlights: • Thermal management for Li-ion batteries using nickel-paraffin is studied. • The temperature is reduced by 31% as compared to natural air cooling mode. • The temperature increases with increase of porosity and pore density of metal foam. • Battery discharge capacity increases with the increase in porosity. • Battery discharge capacity increases with the decreases in pore density.

Ion Mass Spectrometer for Heliospheric Missions

Data.gov (United States)

National Aeronautics and Space Administration — We are developing and IMS that can be used to measure the solar wind ion composition and measure interstellar pick up ions. This instrument will support a future...

Polyaspartate extraction of cadmium ions from contaminated soil: Evaluation and optimization using central composite design.

Science.gov (United States)

Mu'azu, Nuhu Dalhat; Haladu, Shamsuddeen A; Jarrah, Nabeel; Zubair, Mukarram; Essa, Mohammad H; Ali, Shaikh A

2018-01-15

The occurrences of heavy metal contaminated sites and soils and the need for devising environmentally friendly solutions have become global issues of serious concern. In this study, polyaspartate (a highly biodegradable agent) was synthesized using L-Aspartic acid via a new modified thermal procedure and employed for extraction of cadmium ions (Cd) from contaminated soil. Response surface methodology approach using 3 5 full faced centered central composite design was employed for modeling, evaluating and optimizing the influence of polyaspartate concentration (36-145mM), polyaspartate/soil ratio (5-25), initial heavy metal concentration (100-500mg/kg), initial pH (3-6) and extraction time (6-24h) on Cd ions extracted into the polyaspartate solution and its residual concentration in the treated soil. The Cd extraction efficacy obtained reached up to 98.8%. Increase in Cd extraction efficiency was associated with increase in the polyaspartate and Cd concentration coupled with lower polyaspertate/soil ratio and initial pH. Under the optimal conditions characterized with minimal utilization of the polyaspartate and high Cd ions removal, the extractible Cd in the polyaspartate solution reached up to 84.4mg/L which yielded 85% Cd extraction efficacy. This study demonstrates the suitability of using polyaspartate as an effective environmentally friendly chelating agent for Cd extraction from contaminated soils. Copyright © 2017 Elsevier B.V. All rights reserved.

Ion-induced Auger electron spectroscopy: a new detection method for compositional homogeneities of alloyed atoms in silicon

Energy Technology Data Exchange (ETDEWEB)

Hiraki, A [Osaka Univ., Japan; Imura, T; Iwami, M; Kim, S C; Ushita, K; Okamoto, H; Hamakawa, Y

1979-09-01

Auger spectra of Si LMM transitions induced by keV Ar/sup +/ ion bombardment of Si alloy systems have been studied. The spectra observed are composed of two well-defined peaks termed elsewhere the atomic-like and bulk-like peaks, repsectively. A clear correlation has been found between the intensity of the atomic-like peak lying at 88 eV and the content of the foreign atoms alloyed with Si. Experiments were carried out on metallic silicides, or Si alloys with Au, Cu, Pd and Ni, and covalently bonded non-metallic Si alloys of C and H. From these studies, we propose that ion-induced Auger electron spectroscopy might be a useful tool for the determination of alloyed foreign atoms as well as for the study of their compositional homogeneity in binary alloy systems of silicon.

Synthesis of hierarchical conductive C/LiFePO_4/carbon nanotubes composite with less antisite defects for high power lithium-ion batteries

International Nuclear Information System (INIS)

Song, Jianjun; Shao, Guangjie; Ma, Zhipeng; Wang, Guiling; Yang, Jing

2015-01-01

Graphical abstract: The hierarchical conductive C/LiFePO4/CNTs composite with less antisite defects is synthesized by a modified solvothemal process and delivers superior electrochemical performance with high rate capability and good capacity retention. - Abstract: The low electronic conductivity and Li ion diffusion ability are two major obstacles to realize its wide application for LiFePO_4 materials. The material with hierarchical conductive structure and lower antisite defects concentration can effectively enhance the electronic conductivity and Li ion diffusion ability. We firstly report here a modified solvothemal process for the fabrication of hierarchical conductive C/LiFePO_4/CNTs composite with less antisite defects. It is found that the modified solvothemal process is facilitated to decrease Fe_L_i antisite defects and enhance the electronic continuity between LFP and CNTs. In favor of its unique properties, the C/LFP/CNTs composites can deliver superior rate capability and cycling stability. Remarkably, even at a high rate of 20C (3400 mA g"−"1), a high initial discharge capacity of 91.6 mAh g"−"1 and good cycle retention of 95% with almost 100% coulombic efficiency are still obtained after 100 cycles.

Testing electric field models using ring current ion energy spectra from the Equator-S ion composition (ESIC instrument

Directory of Open Access Journals (Sweden)

L. M. Kistler

Full Text Available During the main and early recovery phase of a geomagnetic storm on February 18, 1998, the Equator-S ion composition instrument (ESIC observed spectral features which typically represent the differences in loss along the drift path in the energy range (5–15 keV/e where the drift changes from being E × B dominated to being gradient and curvature drift dominated. We compare the expected energy spectra modeled using a Volland-Stern electric field and a Weimer electric field, assuming charge exchange along the drift path, with the observed energy spectra for H⁺ and O⁺. We find that using the Weimer electric field gives much better agreement with the spectral features, and with the observed losses. Neither model, however, accurately predicts the energies of the observed minima.

Key words. Magnetospheric physics (energetic particles trapped; plasma convection; storms and substorms

Direct detection of ammonium ion by means of oxygen electrocatalysis at a copper-polyaniline composite on a screen-printed electrode

International Nuclear Information System (INIS)

Zhybak, Mykhailo T.; Vagin, Mikhail Yu.; Beni, Valerio; Liu, Xianjie; Turner, Anthony P. F.; Dempsey, Eithne; Korpan, Yaroslav I.

2016-01-01

We describe a composite material for use in electrochemical oxygen reduction. A screen-printed electrode (SPE) was consecutively modified with electrodeposited copper, a Nafion membrane and electropolymerized polyaniline (PANi) to give an electrocatalytic composite of type PANi/Nafion/Cu_2O/SPE that displays good electrical conductivity at neutral pH values. It is found that the presence of ammonia causes complex formation with Cu(I), and this causes electroreduction of oxygen to result in an increased cathodic current. The finding was applied to the quantification of ammonium ions in the 1 to 1000 μM concentration range by amperometry at −0.45 V (vs. Ag/AgCl). This Faradaic phenomenon offers the advantage of direct voltammetric detection, one of the lowest known limits of detection (0.5 μM), and high sensitivity (250 mA∙M"−"1∙cm"−"2). It was applied to the determination of ammonium ion in human serum where it compared well with the photometric routine approach for clinical analysis using glutamate dehydrogenase. (author)

Synthesis of visible-light responsive graphene oxide/TiO(2) composites with p/n heterojunction.

Science.gov (United States)

Chen, Chao; Cai, Weimin; Long, Mingce; Zhou, Baoxue; Wu, Yahui; Wu, Deyong; Feng, Yujie

2010-11-23

Graphene oxide/TiO(2) composites were prepared by using TiCl(3) and graphene oxide as reactants. The concentration of graphene oxide in starting solution played an important role in photoelectronic and photocatalytic performance of graphene oxide/TiO(2) composites. Either a p-type or n-type semiconductor was formed by graphene oxide in graphene oxide/TiO(2) composites. These semiconductors could be excited by visible light with wavelengths longer than 510 nm and acted as sensitizer in graphene oxide/TiO(2) composites. Visible-light driven photocatalytic performance of graphene oxide/TiO(2) composites in degradation of methyl orange was also studied. Crystalline quality and chemical states of carbon elements from graphene oxide in graphene oxide/TiO(2) composites depended on the concentration of graphene oxide in the starting solution. This study shows a possible way to fabricate graphene oxide/semiconductor composites with different properties by using a tunable semiconductor conductivity type of graphene oxide.

Influence of iron substitution by selected rare-earth ions on the properties of NiZn ferrite fillers and PVC magneto-polymer composites

Science.gov (United States)

Ušák, Elemír; Ušáková, Mariana; Dosoudil, Rastislav; Šoka, Martin; Dobročka, Edmund

2018-04-01

Nickel-zinc ferrites are very important soft magnetic materials from the point of view of diverse technical applications (such as, e.g., various electronic devices and components) for their high magnetic permeability and permittivity, low core loss, high resistivity, high Curie temperature as well as mechanical strength and chemical stability. Due to their good absorbing properties, they can be used as microwave absorbing and shielding materials with the aim of decreasing the environmental pollution caused by non-ionizing microwave radiation. The ferrite material incorporated into the polymer matrix creates qualitatively new magneto-polymer composite material taking benefits from both components. The properties typical for polymers (elasticity, mouldability, etc.) are combined with good high-frequency magnetic parameters, thus allowing to utilize these materials, e.g., in high-frequency applications where especially flexibility of composite materials plays a key role. Small amounts of selected rare-earth (RE) ions, in particular Y3+, La3+, Eu3+ and Gd3+ have been embedded into the nickel-zinc ferrite that has been used as the magnetic filler in magnetic polymer composites with polyvinylchloride (PVC) acting as the polymeric matrix. The effect of various types of rare-earth ions on the structural as well as quasi-static and dynamic (electro)magnetic properties of the ferrite fillers as well as ferrite/PVC composites, in particular the frequency dispersion of the complex permeability, has been studied.

Retention of nucleic acids in ion-pair reversed-phase high-performance liquid chromatography depends not only on base composition but also on base sequence.

Science.gov (United States)

Qiao, Jun-Qin; Liang, Chao; Wei, Lan-Chun; Cao, Zhao-Ming; Lian, Hong-Zhen

2016-12-01

The study on nucleic acid retention in ion-pair reversed-phase high-performance liquid chromatography mainly focuses on size-dependence, however, other factors influencing retention behaviors have not been comprehensively clarified up to date. In this present work, the retention behaviors of oligonucleotides and double-stranded DNAs were investigated on silica-based C 18 stationary phase by ion-pair reversed-phase high-performance liquid chromatography. It is found that the retention of oligonucleotides was influenced by base composition and base sequence as well as size, and oligonucleotides prone to self-dimerization have weaker retention than those not prone to self-dimerization but with the same base composition. However, homo-oligonucleotides are suitable for the size-dependent separation as a special case of oligonucleotides. For double-stranded DNAs, the retention is also influenced by base composition and base sequence, as well as size. This may be attributed to the interaction of exposed bases in major or minor grooves with the hydrophobic alky chains of stationary phase. In addition, no specific influence of guanine and cytosine content was confirmed on retention of double-stranded DNAs. Notably, the space effect resulted from the stereostructure of nucleic acids also influences the retention behavior in ion-pair reversed-phase high-performance liquid chromatography. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

In situ reduction of WS{sub 2} nanosheets for WS{sub 2}/reduced graphene oxide composite with superior Li-ion storage

Energy Technology Data Exchange (ETDEWEB)

Zhou, Liyan [Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing, 210093 (China); National Laboratory of Solid State Microstructures, School of Electronic Science and Engineering, Nanjing University, Nanjing, 210093 (China); Yan, Shancheng, E-mail: yansc@njupt.edu.cn [School of Geography and Biological Information, Nanjing University of Posts and Telecommunications, Nanjing, 210023 (China); National Laboratory of Solid State Microstructures, School of Electronic Science and Engineering, Nanjing University, Nanjing, 210093 (China); Lin, Zixia [Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing, 210093 (China); National Laboratory of Solid State Microstructures, School of Electronic Science and Engineering, Nanjing University, Nanjing, 210093 (China); Shi, Yi, E-mail: yshi@nju.edu.cn [Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing, 210093 (China); National Laboratory of Solid State Microstructures, School of Electronic Science and Engineering, Nanjing University, Nanjing, 210093 (China)

2016-03-01

Two-dimensional transition-metal dichalcogenides, such as tungsten disulfide (WS{sub 2}), have been actively studied as suitable candidates for anode materials used in lithium ion batteries recently, due to their remarkable ion intercalation properties. However, the difficulties in the synthesis of phase-pure WS{sub 2}, restacking between WS{sub 2} nanosheets, low electronic conductivity and brittle nature of WS{sub 2} severely limit its Li-ion batteries application. Here, we adopt a one-pot method for synthesizing of WS{sub 2}/reduced Graphene Oxide (rGO) composite to improve the battery performance dramatically. The WS{sub 2}/rGO anode shows a stable discharge capacity of 431.2 mAh/g, at a current density of 0.1 A/g after 100 cycles, while the capacity of bare WS{sub 2} is only 65.5 mAh/g under the same condition. The added graphene oxide is reduced to rGO in reaction process and constitute stable composite with WS{sub 2}, not only avoiding the restacking between WS{sub 2} nanosheets and improving the conductive properties, but also promoting the reduction of WO{sub 3} effectively. Our work may provide a possible route to avoid oxygen impurities in transition metal dichalcogenides. - Highlights: • The WS{sub 2}/rGO composite were synthesized to improve the battery performance. • The WS{sub 2}/rGO anode shows a capacity of 431.2 mAh/g, much higher than WS{sub 2}. • The added graphene oxide is reduced to rGO, improving the conductive properties. • The rGO can avoid the restacking, and promote the reduction of WO{sub 3}.

High quality NMP exfoliated graphene nanosheet-SnO2 composite anode material for lithium ion battery.

Science.gov (United States)

Ravikumar, Raman; Gopukumar, Sukumaran

2013-03-21

A graphene nanosheet-SnO(2) (GNS-SnO(2)) composite is prepared using N-methylpyrrolidone as a solvent to exfoliate graphene from graphite bar with the aid of CTAB by single phase co-precipitation method. The synthesized composites has been characterised physically by powder XRD which confirms the formation of the composite tetragonal SnO(2) crystal system with the low intense broad 002 plane for GNS. The sandwiched morphology of GNS-SnO(2) and the formation of nanosized particles (around 20 nm) have been confirmed by SEM and TEM images. The presence of sp(2) carbon in the GNS is clear by the highly intense G than D band in laser Raman spectroscopy analysis; furthermore, a single chemical shift has been observed at 132.14 ppm from solid-state (13)C NMR analysis. The synthesized composite has been electrochemically characterized using charge-discharge and EIS analysis. The capacity retentions at the end of the first 10 cycles is 57% (100 mA g(-1) rate), the second 10 cycles is 77.83% (200 mA g(-1)), and the final 10 cycles (300 mA g(-1)) is 81.5%. Moreover the impedance analysis clearly explains the low resistance pathway for Li(+) insertion after 30 cycles when compared with the initial cycle. This superior characteristic of GNS-SnO(2) composite suggests that it is a promising candidate for lithium ion battery anode.

Microstructural evolution and mechanical properties of Ti3SiC2-TiC composites

International Nuclear Information System (INIS)

Tian, WuBian; Sun, ZhengMing; Hashimoto, Hitoshi; Du, YuLei

2010-01-01

Ti 3 SiC 2 -TiC composites were fabricated by pulse discharge sintering technique using three different sets of powder mixtures, i.e. Ti/Si/TiC (TC30), Ti/Si/C/TiC (SI30) and Ti/Si/C (TSC30). Based on X-ray diffraction (XRD) analysis and microstructural observations, starting powder reactants were found to have little effect on phase content but strong influence on the microstructure in terms of phase distribution. The phase distribution mainly relies on the heat released from reaction and the liquid phase content formed during sintering. The mechanical properties of the fabricated dense samples demonstrate that more homogeneous phase distribution, available by choosing the starting reactants of SI30, results in higher flexural strength, whereas the Vickers hardness is almost independent of the microstructure. The enhanced flexural strength in sample SI30 sintered at 1400 o C is mainly attributed to the homogeneous TiC distribution in the microstructure.

Method for producing ceramic composition having low friction coefficient at high operating temperatures

Science.gov (United States)

Lankford, Jr., James

1988-01-01

A method for producing a stable ceramic composition having a surface with a low friction coefficient and high wear resistance at high operating temperatures. A first deposition of a thin film of a metal ion is made upon the surface of the ceramic composition and then a first ion implantation of at least a portion of the metal ion is made into the near surface region of the composition. The implantation mixes the metal ion and the ceramic composition to form a near surface composite. The near surface composite is then oxidized sufficiently at high oxidizing temperatures to form an oxide gradient layer in the surface of the ceramic composition.

Hydrothermal synthesis of layer-controlled MoS_2/graphene composite aerogels for lithium-ion battery anode materials

International Nuclear Information System (INIS)

Zhao, Bing; Wang, Zhixuan; Gao, Yang; Chen, Lu; Lu, Mengna; Jiao, Zheng; Jiang, Yong; Ding, Yuanzhang; Cheng, Lingli

2016-01-01

Highlights: • Layer-controlled MoS_2/GA composites are synthesized by a facile hydrothermal route. • Few-layer (5–15 layers) MoS_2 nanosheets are decorated on the surface of GNS homogeneously and tightly. • The growth mechanism of the lay-controlled MoS_2/GA composites is proposed. • The composite delivers high specific capacity of 1085.0 mAh g"−"1 at 0.1 A g"−"1. - Abstract: Layer-controlled MoS_2/graphene aerogels (MoS_2/GA) composites are synthesized by a facile hydrothermal route, in which few-layer (5–15 layers) MoS_2 nanosheets with high crystalline are decorated on the surface of graphene nanosheets homogeneously and tightly. The number of the MoS_2 layers can be easily controlled through adjusting the amount of molybdenum source in the reaction system. Moreover, the growth mechanism of the lay-controlled MoS_2/GA composites is proposed. The three-dimensional MoS_2/GA with macroporous micro-structure not only shortens the transportation length of electrons and ions, but also restrains the re-stacking of MoS_2 effectively, stabilizing the electrode structure during repeated charging/discharging processes. Electrochemical tests demonstrate that this few-layer MoS_2/GA composite exhibits a high reversible capacity of 1085.0 mAh g"−"1 at current density of 100 mA g"−"1, as well as extraordinarily high cycling stability and rate capability.

Development of methodics for the characterization of the composition of the ion-collision-induced secondary-particle flux by comparison of the yield contributions of photoinduced ion formation processes; Entwicklung einer Methodik zur Charakterisierung der Zusammensetzung des ionenbeschussinduzierten Sekundaerteilchenflusses durch Vergleich der Ausbeuteanteile photoinduzierter Ionenbildungsprozesse

Energy Technology Data Exchange (ETDEWEB)

Vering, Guido

2008-10-13

The aim of this work was to develop a method to distinguish between different ion formation processes and to determine the influence of these processes on the total number of detected monatomic ions of a certain element. A vector/matrix-formalism was developed, which describes the physical processes of sputtering, ion formation, mass separation and detection in laser-SNMS. In the framework of the method developed, based on this theoretic formalism, changes in the secondary flux contribution of the respective element were observed by comparing the detected monatomic ion yield obtained in specifically aligned (SIMS and) laser-SNMS experiments. The yields resulting from these experiments were used to calculate characteristic numbers to compare the flux composition from different surfaces. The potential of the method was demonstrated for the elements boron, iron and gadolinium by investigating the changes in the flux composition of secondary particles sputtered from metallic surfaces, as a function of the oxygen concentration at the surface. Finally, combined laser-SNMS depth profiles and images, obtained with both laser systems, were presented to demonstrate how the parallel detection of the three differently originated ion signals of the same element can be used to get additional information about the composition of the flux of secondary particles synchronously during the analysis of elemental distributions. In this respect the presented method can be a very helpful tool to prevent misleading interpretations of SIMS or laser-SNMS data. (orig.)

Synthesis and electrochemical performance of Li2FeSiO4/C/carbon nanosphere composite cathode materials for lithium ion batteries

International Nuclear Information System (INIS)

Yang, Jinlong; Kang, Xiaochun; Hu, Lin; Gong, Xue; He, Daping; Peng, Tao; Mu, Shichun

2013-01-01

Highlights: •The Li 2 FeSiO 4 /C/CNS was prepared by effective double-carbon composite route. •The CNS as the conductivity belt connects the Li 2 FeSiO 4 /C particles. •The samples have a high capacity and excellent cyclic and rate performance. -- Abstract: Li 2 FeSiO 4 /C/carbon nanosphere (CNS) composites as cathode materials for lithium-ion batteries were synthesized by a simple hydro-chemical method. The double-carbon structural design of glucose pyrolysis-carbon (C) and CNS improved electrochemical performance of the composite where the CNS can build conductivity belts to connect the Li 2 FeSiO 4 /C particles and to favor electronic transmission. The exchange current density and the diffusion coefficient of lithium ions with the composite were 0.208 mA cm −2 and 1.06E−11 cm 2 S −1 , respectively, which were much larger than that of conventional Li 2 FeSiO 4 /C composite cathode materials (i = 0.131 mA cm −2 , D Li = 4.69E−12 cm 2 S −1 ). The electrochemical test results showed that the discharge capacity of 164.7 mA h g −1 could be obtained, and especially, after 60 cycles, 98.4% of the initial discharge capacity remained at 0.1 C of galvanostatic discharge in the potential range of 1.5–4.8 V (vs. Li/Li + ). In addition, the discharge capacity of 92.4 mA h g −1 at 5 C was easily recovered to 159.8 mA h g −1 at 0.1 C

Hierarchical architecture of ReS_2/rGO composites with enhanced electrochemical properties for lithium-ion batteries

International Nuclear Information System (INIS)

Qi, Fei; Chen, Yuanfu; Zheng, Binjie; He, Jiarui; Li, Qian; Wang, Xinqiang; Lin, Jie; Zhou, Jinhao; Yu, Bo; Li, Pingjian; Zhang, Wanli

2017-01-01

Highlights: • The ReS_2/rGO composites have been synthesized by a facile one-pot method. • The ReS_2/rGO composites exhibit hierarchical architecture. • The ReS_2/rGO composites deliver better electrochemical performances than ReS_2. • The enhanced performance is due to porous and conductive structure of ReS_2/rGO. - Abstract: Rhenium disulfide (ReS_2), a two-dimensional (2D) semiconductor, has attracted more and more attention due to its unique anisotropic electronic, optical, mechanical properties. However, the facile synthesis and electrochemical property of ReS_2 and its composite are still necessary to be researched. In this study, for the first time, the ReS_2/reduced graphene oxide (rGO) composites have been synthesized through a facile and one-pot hydrothermal method. The ReS_2/rGO composites exhibit a hierarchical, interconnected, and porous architecture constructed by nanosheets. As anode for lithium-ion batteries, the as-synthesized ReS_2/rGO composites deliver a large initial capacity of 918 mAh g"−"1 at 0.2 C. In addition, the ReS_2/rGO composites exhibit much better electrochemical cycling stability and rate capability than that of bare ReS_2. The significant enhancement in electrochemical property can be attributed to its unique architecture constructed by nanosheets and porous structure, which can allow for easy electrolyte infiltration, efficient electron transfer, and ionic diffusion. Furthermore, the graphene with high electronic conductivity can provide good conductive passageways. The facile synthesis approach can be extended to prepare other 2D transition metal dichalcogenides semiconductors for energy storage and catalytic application.

Spatial atomic layer deposition on flexible porous substrates: ZnO on anodic aluminum oxide films and Al2O3 on Li ion battery electrodes

International Nuclear Information System (INIS)

Sharma, Kashish; Routkevitch, Dmitri; Varaksa, Natalia; George, Steven M.

2016-01-01

Spatial atomic layer deposition (S-ALD) was examined on flexible porous substrates utilizing a rotating cylinder reactor to perform the S-ALD. S-ALD was first explored on flexible polyethylene terephthalate polymer substrates to obtain S-ALD growth rates on flat surfaces. ZnO ALD with diethylzinc and ozone as the reactants at 50 °C was the model S-ALD system. ZnO S-ALD was then performed on nanoporous flexible anodic aluminum oxide (AAO) films. ZnO S-ALD in porous substrates depends on the pore diameter, pore aspect ratio, and reactant exposure time that define the gas transport. To evaluate these parameters, the Zn coverage profiles in the pores of the AAO films were measured using energy dispersive spectroscopy (EDS). EDS measurements were conducted for different reaction conditions and AAO pore geometries. Substrate speeds and reactant pulse durations were defined by rotating cylinder rates of 10, 100, and 200 revolutions per minute (RPM). AAO pore diameters of 10, 25, 50, and 100 nm were utilized with a pore length of 25 μm. Uniform Zn coverage profiles were obtained at 10 RPM and pore diameters of 100 nm. The Zn coverage was less uniform at higher RPM values and smaller pore diameters. These results indicate that S-ALD into porous substrates is feasible under certain reaction conditions. S-ALD was then performed on porous Li ion battery electrodes to test S-ALD on a technologically important porous substrate. Li 0.20 Mn 0.54 Ni 0.13 Co 0.13 O 2 electrodes on flexible metal foil were coated with Al 2 O 3 using 2–5 Al 2 O 3 ALD cycles. The Al 2 O 3 ALD was performed in the S-ALD reactor at a rotating cylinder rate of 10 RPM using trimethylaluminum and ozone as the reactants at 50 °C. The capacity of the electrodes was then tested versus number of charge–discharge cycles. These measurements revealed that the Al 2 O 3 S-ALD coating on the electrodes enhanced the capacity stability. This S-ALD process could be extended to roll-to-roll operation for

Earliest Results in the Use of Activated Composite Membranes for the Transport of Silver Ions from Aqueous Solutions

Directory of Open Access Journals (Sweden)

Yucundo Mendoza-Tolentino

2014-01-01

Full Text Available This paper presents the results concerning the first use of activated composite membranes (ACMs for the facilitated transport of silver ions containing di-(2-ethylhexyl-dithiophosphoric acid (DTPA as the carrier. DTPA was immobilized by interfacial polymerization in a dense layer that was deposited in a porous layer, which was prepared on a nonwoven fabric support by phase inversion. The influence of fundamental parameters affecting the transport of silver ion as the carrier concentration in the membrane phase and stripping agent variation of the stripping solution have been studied. In the optimal conditions, the amount of silver transported across the ACMs was greater than 50%, whereas if the content of the carrier is modified, more than the 90% of the initial silver is removed from the feed phase.

Methods of gas purification and effect on the ion composition in an RF atmospheric pressure plasma jet investigated by mass spectrometry

International Nuclear Information System (INIS)

Grosse-Kreul, Simon; Huebner, Simon; Schneider, Simon; Keudell, Achim von; Benedikt, Jan

2016-01-01

The analysis of the ion chemistry of atmospheric pressure plasmas is essential to evaluate ionic reaction pathways during plasma-surface or plasma-analyte interactions. In this contribution, the ion chemistry of a radio-frequency atmospheric pressure plasma jet (μ-APPJ) operated in helium is investigated by mass spectrometry (MS). It is found, that the ion composition is extremely sensitive to impurities such as N 2 , O 2 and H 2 O. Without gas purification, protonated water cluster ions of the form H + (H 2 O) n are dominating downstream the positive ion mass spectrum. However, even after careful feed gas purification to the sub-ppm level using a molecular sieve trap and a liquid nitrogen trap as well as operation of the plasma in a controlled atmosphere, the positive ion mass spectrum is strongly influenced by residual trace gases. The observations support the idea that species with a low ionization energy serve as a major source of electrons in atmospheric pressure helium plasmas. Similarly, the neutral density of atomic nitrogen measured by MS in a He/N 2 mixture is varying up to a factor 3, demonstrating the significant influence of impurities on the neutral species chemistry as well. (orig.)

IMP-8 observations of the spectra, composition, and variability of solar heavy ions at high energies relevant to manned space missions

International Nuclear Information System (INIS)

Tylka, Allan J.; Dietrich, William F.

1999-01-01

In more than 25 years of almost continuous observations, the University of Chicago's Cosmic Ray Telescope (CRT) on IMP-8 has amassed a unique database on high-energy solar heavy ions of potential relevance to manned spaceflight. In the very largest particle events, IMP-8/CRT has even observed solar Fe ions above the Galactic cosmic ray background up to ∼800 MeV/nucleon, an energy sufficiently high to penetrate nearly 25 g/cm 2 of shielding. IMP-8/CRT observations show that high-energy heavy-ion spectra are often surprisingly hard power laws, without the exponential roll-offs suggested by stochastic acceleration fits to lower energy measurements alone. Also, in many solar particle events the Fe/O ratio grows with increasing energy, contrary to the notion that ions with higher mass-to-charge ratios should be less abundant at higher energies. Previous studies of radiation hazards for manned spaceflight have often assumed heavy-ion composition and steeply-falling energy spectra inconsistent with these observations. Conclusions based on such studies should therefore be re-assessed. The significant event-to-event variability observed in the high-energy solar heavy ions also has important implications for strategies in building probabilistic models of solar particle radiation hazards

Methods of gas purification and effect on the ion composition in an RF atmospheric pressure plasma jet investigated by mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Grosse-Kreul, Simon; Huebner, Simon; Schneider, Simon; Keudell, Achim von; Benedikt, Jan [Ruhr-Universitaet Bochum, Institute for Experimental Physics II, Bochum (Germany)

2016-12-15

The analysis of the ion chemistry of atmospheric pressure plasmas is essential to evaluate ionic reaction pathways during plasma-surface or plasma-analyte interactions. In this contribution, the ion chemistry of a radio-frequency atmospheric pressure plasma jet (μ-APPJ) operated in helium is investigated by mass spectrometry (MS). It is found, that the ion composition is extremely sensitive to impurities such as N{sub 2}, O{sub 2} and H{sub 2}O. Without gas purification, protonated water cluster ions of the form H{sup +}(H{sub 2}O){sub n} are dominating downstream the positive ion mass spectrum. However, even after careful feed gas purification to the sub-ppm level using a molecular sieve trap and a liquid nitrogen trap as well as operation of the plasma in a controlled atmosphere, the positive ion mass spectrum is strongly influenced by residual trace gases. The observations support the idea that species with a low ionization energy serve as a major source of electrons in atmospheric pressure helium plasmas. Similarly, the neutral density of atomic nitrogen measured by MS in a He/N{sub 2} mixture is varying up to a factor 3, demonstrating the significant influence of impurities on the neutral species chemistry as well. (orig.)

Si/C composite lithium-ion battery anodes synthesized from coarse silicon and citric acid through combined ball milling and thermal pyrolysis

International Nuclear Information System (INIS)

Gu Peng; Cai Rui; Zhou Yingke; Shao Zongping

2010-01-01

Silicon and related materials have recently received considerable attention as potential anodes in Li-ion batteries for their high theoretical specific capacities. To overcome the problem of volume variations during the Li insertion/extraction process, in this work, Si/C composites with low carbon content were synthesized from cheap coarse silicon and citric acid by simple ball milling and subsequent thermal treatment. The effects of ball milling time and calcination temperature on the structure, composition and morphology of the composites were systematically investigated by the determination of specific surface area (BET) and particle-size distribution, X-ray diffraction (XRD), O 2 -TPO, and scanning electron microscopy (SEM). The capacity and cycling stability of the composites were systematically evaluated by electrochemical charge/discharge tests. It was found that both the initial capacity and the cycling stability of the composites were dependent on the milling and calcination conditions, and attractive overall electrochemical performance could be obtained by optimizing the synthesis process.