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Sample records for surface-converter h ion

  1. Dissociative recombination of molecular ions H2+

    International Nuclear Information System (INIS)

    Abarenov, A.V.; Marchenko, V.S.

    1989-01-01

    The total cross sections of dissociation and dissociative recombination of slow electrons and molecular ions H 2 + have been calculated in terms of the quasiclassical and dipole approximations. In the calculations allowance was made for the quantum nature of vibrational motion of heavy particles and presence of autoionization of divergence states of the H 2 (Σ u , nl) molecules. It is shown that the H 2 + ion dissociation cross sections are dominant in increase of the electron energy in the ε >or approx. 2-3 eV region for H 2 + (v) ion distribution over the vibrational levels characteristic for the beam experiments. 15 refs.; 5 figs

  2. Optically pumped polarized H- ion source

    International Nuclear Information System (INIS)

    Anderson, L.W.

    1986-01-01

    The current status and future prospects for the optically pumped polarized H - ion source are discussed. At the present time H - ion currents of 60 μA and with a polarization of 65% have been produced. The ion current and polarization can be increased significantly if the optically pumped Na charge exchange target density and polarization can be increased. Studies of wall surfaces that permit many bounces before depolarizing the Na electron spin and studies of radiation trapping in optically pumped Na indicate that the Na target density and polarization can be increased substantially. 27 refs., 6 figs., 2 tabs

  3. Helicon plasma generator-assisted surface conversion ion source for the production of H(-) ion beams at the Los Alamos Neutron Science Center.

    Science.gov (United States)

    Tarvainen, O; Rouleau, G; Keller, R; Geros, E; Stelzer, J; Ferris, J

    2008-02-01

    The converter-type negative ion source currently employed at the Los Alamos Neutron Science Center (LANSCE) is based on cesium enhanced surface production of H(-) ion beams in a filament-driven discharge. In this kind of an ion source the extracted H(-) beam current is limited by the achievable plasma density which depends primarily on the electron emission current from the filaments. The emission current can be increased by increasing the filament temperature but, unfortunately, this leads not only to shorter filament lifetime but also to an increase in metal evaporation from the filament, which deposits on the H(-) converter surface and degrades its performance. Therefore, we have started an ion source development project focused on replacing these thermionic cathodes (filaments) of the converter source by a helicon plasma generator capable of producing high-density hydrogen plasmas with low electron energy. In our studies which have so far shown that the plasma density of the surface conversion source can be increased significantly by exciting a helicon wave in the plasma, and we expect to improve the performance of the surface converter H(-) ion source in terms of beam brightness and time between services. The design of this new source and preliminary results are presented, along with a discussion of physical processes relevant for H(-) ion beam production with this novel design. Ultimately, we perceive this approach as an interim step towards our long-term goal, combining a helicon plasma generator with an SNS-type main discharge chamber, which will allow us to individually optimize the plasma properties of the plasma cathode (helicon) and H(-) production (main discharge) in order to further improve the brightness of extracted H(-) ion beams.

  4. H- ion production from different converter materials

    International Nuclear Information System (INIS)

    Leung, K.N.; Ehlers, K.W.

    1984-10-01

    For heating plasmas and for current drive in some fusion reactors, high energy neutral beams may be required. The high neutralization efficiency of H - or D - ions makes them favorable to form neutral atoms with energies in excess of 160 keV. It has been shown that a steady-state H - ion beam with current greater than 1 A can be generated by a surface conversion type source with Mo being used as the converter material. In order to achieve the proper cesium coverage and thereby increasing the H - ion yield, the application of porous cesium-dispensing converters is being investigated. It is also possible to optimize the H - production by choosing the proper converter material. In this paper, we compare the negative ion yield generated by different materials (such as Mo, Ti, V, Nb, Pt, Pd, Rh, Cu, Ta, Al, Au, LaB 6 and stainless-steel) in the pure hydrogen and cesium-hydrogen modes of operation

  5. Multiquanta photodetachment from the H- ion

    International Nuclear Information System (INIS)

    Tang, Chen-Yau.

    1992-03-01

    Multiphoton detachment (MPD) of an electron from the loosely bound H - system (binding energy = 0.7542 eV) has been studied at various photon energies and laser intensities. In the center of mass of 800-MeV H - ions the CO 2 laser photon energy, 0.117 eV, was Doppler tuned over a wide range, from 0.15 to 0.39 eV. The peak laser intensity in the lab frame was varied from 2 to 12 GW/cm 2 . The general behavior of MPD versus photon energy and the ac-Stark/pondermotive effects are of special interest in the study. Characteristic threshold structures by absorption of 2, 3, 4, and 5 photons were observed, as evidenced by rapid changes in the signal amplitudes. These thresholds provide a straightforward picture of channel opening in MPD as the photon energy is increased. A fit of two-photon detachment data to the Wigner threshold law showed a good match with a small intensity-induced shift in the threshold energy. A study of laser intensity effects demonstrated departures from the simple power law predicted by lowest-order perturbation theory, which is possibly another indication of pondermotive shifts in the threshold. The absolute MPD rates have been estimated and found to be in fairly good agreement with the results of Floquet theory

  6. Rotation characteristics of main ions and impurity ions in H-mode tokamak plasma

    International Nuclear Information System (INIS)

    Kim, J.; Burrell, K.H.; Gohil, P.; Groebner, R.J.; Kim, Y.; St. John, H.E.; Seraydarian, R.P.; Wade, M.R.

    1994-01-01

    Poloidal and toroidal rotation of the main ions (He 2+ ) and the impurity ions (C 6+ and B 5+ ) in H-mode helium plasmas have been measured via charge exchange recombination spectroscopy in the DIII-D tokamak. It was discovered that the main ion poloidal rotation is in the ion diamagnetic drift direction while the impurity ion rotation is in the electron diamagnetic drift direction, in qualitative agreement with the neoclassical theory. The deduced radial electric field in the edge is of the same negative-well shape regardless of which ion species is used, validating the fundamental nature of the electric field in L-H transition phenomenology

  7. Study on a volume-production H- ion source

    International Nuclear Information System (INIS)

    Takama, S.

    1988-01-01

    H - ions formed by volume-production are extracted from a multicuspion source. By applying a large positive bias to the plasma electrode, the ratio I - /I e becomes 1/20. H - ion current of 0.4mA is extracted from a 0.3cm 2 circular aperture at an arc current of 10A. (author)

  8. Ion transport in a pH-regulated nanopore.

    Science.gov (United States)

    Yeh, Li-Hsien; Zhang, Mingkan; Qian, Shizhi

    2013-08-06

    Fundamental understanding of ion transport phenomena in nanopores is crucial for designing the next-generation nanofluidic devices. Due to surface reactions of dissociable functional groups on the nanopore wall, the surface charge density highly depends upon the proton concentration on the nanopore wall, which in turn affects the electrokinetic transport of ions, fluid, and particles within the nanopore. Electrokinetic ion transport in a pH-regulated nanopore, taking into account both multiple ionic species and charge regulation on the nanopore wall, is theoretically investigated for the first time. The model is verified by the experimental data of nanopore conductance available in the literature. The results demonstrate that the spatial distribution of the surface charge density at the nanopore wall and the resulting ion transport phenomena, such as ion concentration polarization (ICP), ion selectivity, and conductance, are significantly affected by the background solution properties, such as the pH and salt concentration.

  9. Development of a multicusp H- ion source for accelerator applications

    International Nuclear Information System (INIS)

    York, R.L.; Stevens, R.R. Jr.

    1983-01-01

    The development of a multicusp surface-production H - ion source (Berkeley concept) designed specifically for accelerator use is described. The goal of this development effort has been to provide a suitable H - ion source for the Proton Storage Ring now being constructed at LAMPF. The ion source that has been developed is now capable of long-term operation at 20 mA of H - current at 10% duty factor and with normalized beam emittance of 0.13 cm-mrad (95% beam fraction). The development program will be described with particular emphasis on beam emittance measurements

  10. Photodetachment of H ion in crossed gradient electric and magnetic ...

    Indian Academy of Sciences (India)

    2016-10-13

    Oct 13, 2016 ... ion in crossed gradient electric and magnetic fields and put forward an analytical formula for calculating the photodetachment cross-section. Compared to the photodetach- ment of H. − ion in a gradient electric field, the Hamiltonian of the detached electron has three degrees of freedom, which makes the ...

  11. Electron paramagnetic resonance parameters of Mn4+ ion in h ...

    Indian Academy of Sciences (India)

    The EPR parameters ( factors ∥, ⊥ and zero-field splitting ) of Mn4+ ion in h-BaTiO3 crystal are calculated from the complete high-order perturbation formulas based on a two-mechanism model for the EPR parameters of 33 ions in trigonal symmetry. In the model, not only the widely used crystal-field mechanism, ...

  12. Ion H2+ can dissociate in a strong magnetic field

    International Nuclear Information System (INIS)

    Turbiner, A.V.; Lopez, J.C.; Flores-Riveros, A.

    2001-01-01

    In framework of a variational method the molecular ion H 2 + in a magnetic field is studied. An optimal form of the vector potential corresponding to a given magnetic field is chosen. It is shown that for any magnetic field strength as well as for any orientation of the molecular axis the system (ppe) possesses a minimum in the potential energy. The stable configuration always corresponds to elongation along the magnetic line. However, for magnetic fields B ≥ 5 x 10 11 G and some orientations the ion H 2 + becomes instable decaying to H-atom + p [ru

  13. Two approaches for $H^{-}$ ion production with 245 GHz ion sources

    CERN Document Server

    Gobin, R; Bacal, M; Breton, J; Delferrière, O; Harrault, F; Ivanov, A A; Svarnas, P; Tuske, O

    2006-01-01

    Over the last few years, the accelerator community requested the development of improved negative hydrogen ion sources. For spallation sources, like SNS or ESS, pulsed high intensity H/sup negative ion beams of a few tens of milliamperes, with a duty cycle close to 10%, are required. New facilities like CERN also ask for high performance negative ion beams. Since CEA undertook an electron cyclotron resonance (ECR)-based ion source programme, a European network devoted to high performance negative ion source development has been created. In this group, several laboratories developing 2.45 GHz ECR sources follow different approaches to increase the extracted ion current. At Saclay, with a solenoidal magnetic structure based on coils, close to 3 mA H/sup negative ion beam is now extracted in pulsed mode (2 ms/100 ms). A metallic biased grid separates the plasma bulk from the H/sup negative ion production zone and significantly improves the H/sup negative extracted current. At Ecole Polytechnique, the source Came...

  14. H- Ion Sources For CERN’s Linac4

    CERN Document Server

    Lettry, J; Coutron, Y; Chaudeta, E; Dallocchio, A; Gil Flores, J; Hansen, J; Mahner, E; Mathot, S; Mattei, S; Midttun, O; Moyret, P; Nisbet, D; O’Neil, M; Paoluzzi, M; Pasquino, C; Pereira, H; Sanchez Arias, J; Schmitzer, C; Scrivens, R; Steyaert, D

    2013-01-01

    The specifications set to the Linac4 ion source are: H- ion pulses of 0.5 ms duration, 80 mA intensity and 45 keV energy within a normalized emittance of 0.25 mmmrad RMS at a repetition rate of 2 Hz. In 2010, during the commissioning of a prototype based on H- production from the plasma volume, it was observed that the powerful co-extracted electron beam inherent to this type of ion source could destroy its electron beam dump well before reaching nominal parameters. However, the same source was able to provide 80 mA of protons mixed with a small fraction of H2+ and H3+ molecular ions. The commissioning of the radio frequency quadrupole accelerator (RFQ), beam chopper and H- beam diagnostics of the Linac4 are scheduled for 2012 and its final installation in the underground building is to start in 2013. Therefore, a crash program was launched in 2010 and reviewed in 2011 aiming at keeping the original Linac4 schedule with the following deliverables: Design and production of a volume ion source prototype suitabl...

  15. Photodetachment of H ion in crossed gradient electric and magnetic ...

    Indian Academy of Sciences (India)

    2016-10-13

    Oct 13, 2016 ... ers used the traditional quantum-mechanical approach ... gen atom is a spherically symmetric, short-ranged ... z y r. -e. + x. H. Figure 1. The schematic plot of H. − ion in crossed gradient electric and magnetic fields. The magnetic field H0 is along the +z-axis and the gradient electric field F is along the x-axis.

  16. Characterization of TRIUMF dc H- ion sources for enhanced brightness

    Science.gov (United States)

    Hwang, Y. S.; Cojocaru, G.; Yuan, D.; McDonald, M.; Jayamanna, K.; Kim, G. H.; Dutto, G.

    2006-03-01

    At TRIUMF, H- ion sources have been characterized on a teststand to improve the understanding of their performance. Measured beam characteristics such as current, emittance, and e /H- ratio were correlated with source conditions as a function of relevant plasma parameters. Plasma densities, temperatures, and plasma potentials were measured with a Langmuir probe and correlated with beam properties for different confining magnetic fields and different values of arc power and gas pressure. The mechanism of beam extraction was studied by correlating plasma potential profiles with the corresponding plasma electrode bias voltages obtained from optimizing ion source outputs. Experiments with collar biasing and noble gas mixing were unsuccessful because of undesirable plasma potential profiles.

  17. Estimation of Sputtering Damages on a Magnetron H- Ion Source Induced by Cs+ and H+ Ions

    CERN Document Server

    Pereira, H; Alessi, J; Kalvas, t

    2013-01-01

    An H− ion source is being developed for CERN’s Linac4 accelerator. A beam current requirement of 80 mA and a reliability above 99% during 1 year with 3 month uninterrupted operation periods are mandatory. To design a low-maintenance long life-time source, it is important to investigate and understand the wear mechanisms. A cesiated plasma discharge ion source, such as the BNL magnetron source, is a good candidate for the Linac4 ion source. However, in the magnetron source operated at BNL, the removal of material from the molybdenum cathode and the stainless steel anode cover plate surfaces is visible after extended operation periods. The observed sputtering traces are shown to result from cesium vapors and hydrogen gas ionized in the extraction region and subsequently accelerated by the extraction field. This paper presents a quantitative estimate of the ionization of cesium and hydrogen by the electron and H− beams in the extraction region of BNL’s magnetron ion source. The respective contributions o...

  18. The TRIUMF optically-pumped polarized H- ion source

    International Nuclear Information System (INIS)

    Levy, C.D.P.; Jayamanna, K.; McDonald, M.; Schmor, P.W.; Van Oers, W.T.H.; Welz, J.; Wight, G.W.; Dutto, G.; Zelenski, A.N.; Sakae, T.

    1995-09-01

    The TRIUMF dc optically-pumped polarized H - ion source (OPPIS) produces 200 μA dc H - current at 85% polarization within a normalized emittance (90%) of 0.8 π mm mrad, for operations at the TRIUMF cyclotron. As a result of development of the ECR primary proton source, 1.6 mA dc polarized H - current is produced within a normalized emittance of 2 π mm mrad, suitable for high energy accelerators. The OPPIS has also been developed for use in a parity non-conservation experiment which has very severe limits on permissible helicity-correlated changes in beam current and energy. (author)

  19. The TRIUMF optically-pumped polarized H- ion source

    International Nuclear Information System (INIS)

    Levy, C.D.P.; Jayamanna, K.; McDonald, M.

    1995-09-01

    The TRIUMF dc optically-pumped polarized H - ion source (OPPIS) produces 200 microA dc H - current at 85% polarization within a normalized emittance (90%) of 0.8 π mm mrad, for operations at the TRIUMF cyclotron. As a result of development of the ECR primary proton source, 1.6 mA dc polarized H - current is produced within a normalized emittance of 2 π mm mrad, suitable for high energy accelerators. The OPPIS has also been developed for use in a parity non-conservation experiment which has very severe limits on permissible helicity-correlated changes in beam current and energy

  20. Computational Tools for Interpreting Ion Channel pH-Dependence.

    Directory of Open Access Journals (Sweden)

    Ivan Sazanavets

    Full Text Available Activity in many biological systems is mediated by pH, involving proton titratable groups with pKas in the relevant pH range. Experimental analysis of pH-dependence in proteins focusses on particular sidechains, often with mutagenesis of histidine, due to its pKa near to neutral pH. The key question for algorithms that predict pKas is whether they are sufficiently accurate to effectively narrow the search for molecular determinants of pH-dependence. Through analysis of inwardly rectifying potassium (Kir channels and acid-sensing ion channels (ASICs, mutational effects on pH-dependence are probed, distinguishing between groups described as pH-coupled or pH-sensor. Whereas mutation can lead to a shift in transition pH between open and closed forms for either type of group, only for pH-sensor groups does mutation modulate the amplitude of the transition. It is shown that a hybrid Finite Difference Poisson-Boltzmann (FDPB - Debye-Hückel continuum electrostatic model can filter mutation candidates, providing enrichment for key pH-coupled and pH-sensor residues in both ASICs and Kir channels, in comparison with application of FDPB alone.

  1. Electron capture by C2+ and Ti2+ ions in H and H2

    International Nuclear Information System (INIS)

    Nutt, W.L.; McCullough, R.W.; Gilbody, H.B.

    1978-01-01

    Cross sections for electron capture by C 2+ and Ti 2+ ions in H and H 2 have been determined within the energy range 0.5 to 14 keV from measurements made using a tungsten-tube furnace to provide a target of highly dissociated hydrogen. (author)

  2. Note: Recombination of H+ and OH− ions along water wires

    International Nuclear Information System (INIS)

    Lee, Song Hi; Rasaiah, Jayendran C.

    2013-01-01

    Transport and recombination of hydrogen and hydroxide ions along a hydrogen-bonded water wire are studied by molecular dynamics simulation using a dissociating model for water. The results are compared with a recent CP-MD study of neutralization in bulk water [A. Hassanali, M. K. Prakrash, H. Eshet, and M. Parrinello, Proc. Natl. Acad. Sci. U.S.A. 108, 20410 (2011)]. The translocation of H + and OH − along the wire is faster than in the bulk water, followed by compression of the water wire when two water molecules separate the transported ions. Neutralization occurs with the concerted transfer of three protons as in the bulk water, followed by energy dissipation along the water chain

  3. Electron paramagnetic resonance parameters of Mn4+ ion in h ...

    Indian Academy of Sciences (India)

    569–575. Electron paramagnetic resonance parameters of Mn4+ ion in h-BaTiO3 crystal from a two-mechanism model. WU XIAO-XUAN1,4,∗, FANG WANG2, FENG WEN-LIN2,3 and. ZHENG WEN-CHEN2,4. 1Department of Physics, Civil Aviation Flight University of China, Guanghan 618307,. People's Republic of China.

  4. Linac4 H{sup −} ion sources

    Energy Technology Data Exchange (ETDEWEB)

    Lettry, J., E-mail: Jacques.lettry@cern.ch; Aguglia, D.; Andersson, P.; Bertolo, S.; Butterworth, A.; Coutron, Y.; Dallocchio, A.; David, N.; Chaudet, E.; Fink, D. A.; Garlasche, M.; Grudiev, A.; Guida, R.; Hansen, J.; Haase, M.; Jones, A.; Koszar, I.; Lallement, J.-B.; Lombardi, A. M.; Machado, C. [CERN-ABP, 1211 Geneva 23 (Switzerland); and others

    2016-02-15

    CERN’s 160 MeV H{sup −} linear accelerator (Linac4) is a key constituent of the injector chain upgrade of the Large Hadron Collider that is being installed and commissioned. A cesiated surface ion source prototype is being tested and has delivered a beam intensity of 45 mA within an emittance of 0.3 π ⋅ mm ⋅ mrad. The optimum ratio of the co-extracted electron- to ion-current is below 1 and the best production efficiency, defined as the ratio of the beam current to the 2 MHz RF-power transmitted to the plasma, reached 1.1 mA/kW. The H{sup −} source prototype and the first tests of the new ion source optics, electron-dump, and front end developed to minimize the beam emittance are presented. A temperature regulated magnetron H{sup −} source developed by the Brookhaven National Laboratory was built at CERN. The first tests of the magnetron operated at 0.8 Hz repetition rate are described.

  5. The BNL polarized H- ion source development program

    International Nuclear Information System (INIS)

    Kponou, A.; Alessi, J.; Hershcovitch, A.; DeVito, B.

    1992-01-01

    Polarized protons have been available for acceleration in the AGS for the high energy physics program since 1984. The polarized H - source, PONI-1, has routinely supplied a 0.4 Hz, 400 μsec pulse having a nominal intensity of 40 μA. Polarization is ∼80% out of the ion source. After PONI- 1 became operational, a program was initiated to develop a more intense source based on a cold ground state atomic beam source, followed by ionization of the polarized H degrees beam by D - charge exchange. Various phases of this work have been fully reported elsewhere, and only a summary is given here

  6. 21 CFR 868.1170 - Indwelling blood hydrogen ion concentration (pH) analyzer.

    Science.gov (United States)

    2010-04-01

    ... Indwelling blood hydrogen ion concentration (pH) analyzer. (a) Identification. An indwelling blood hydrogen ion concentration (pH) analyzer is a device that consists of a catheter-tip pH electrode and that is... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Indwelling blood hydrogen ion concentration (pH...

  7. Temperature dependence of third order ion molecule reactions. The reaction H+3 + 2H2 = H+5 + H2

    International Nuclear Information System (INIS)

    Hiraoka, K.; Kebarle, P.

    1975-01-01

    The rate constants k 1 for Reaction (1): H + 3 +2H 2 = H + 5 +H 2 were measured in the temperature range 100--300 degreeK. The temperature dependence of k 1 has the form k 1 proportionalT - /subn/, where n=2.3. Pierce and Porter have reported a much stronger negative temperature dependence with n=4.6. The difference arises from a determination of k 1 at 300 degreeK obtained by Arifov and used by Porter. The present k 1 (300 degreeK) =9times10 -30 (cm 6 molecules -2 center-dotsec -1 ). This is more than an order of magnitude larger than the Arifov value. The temperature dependence of third body dependent association reactions like (1) is examined on the basis of the energy transfer theory and the recently proposed trimolecular complex transition state theory by Meot-Ner, Solomon, Field, and Gershinowitz. The temperature dependence of the rate constant for the reverse reaction (-1) is obtained from k 1 and the previously determined temperature dependence of the equilibria (1). k/sub -//sub 1/ gives a good straight line Arrhenius plot leading to k/sub -//sub 1/ =8.7times10 -6 exp(-8.4/RT) cm 3 molecules -1 center-dotsec -1 . The activation energy is in kcal/mole. The preexponential factor is much larger than the rate constant for Langevin collisions. This is typical for pyrolysis of ions involving second order activation

  8. H- Ion Sources for High Intensity Proton Drivers

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Rolland Paul [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Dudnikov, Vadim [Muons, Inc., Batavia, IL (United States)

    2015-02-20

    Existing RF Surface Plasma Sources (SPS) for accelerators have specific efficiencies for H+ and H- ion generation around 3 to 5 mA/cm2 per kW, where about 50 kW of RF power is typically needed for 50 mA beam current production. The Saddle Antenna (SA) SPS described here was developed to improve H- ion production efficiency, reliability and availability for pulsed operation as used in the ORNL Spallation Neutron Source . At low RF power, the efficiency of positive ion generation in the plasma has been improved to 200 mA/cm2 per kW of RF power at 13.56 MHz. Initial cesiation of the SPS was performed by heating cesium chromate cartridges by discharge as was done in the very first versions of the SPS. A small oven to decompose cesium compounds and alloys was developed and tested. After cesiation, the current of negative ions to the collector was increased from 1 mA to 10 mA with RF power 1.5 kW in the plasma (6 mm diameter emission aperture) and up to 30 mA with 4 kW RF power in the plasma and 250 Gauss longitudinal magnetic field. The ratio of electron current to negative ion current was improved from 30 to 2. Stable generation of H- beam without intensity degradation was demonstrated in the aluminum nitride (AlN) discharge chamber for 32 days at high discharge power in an RF SPS with an external antenna. Some modifications were made to improve the cooling and cesiation stability. The extracted collector current can be increased significantly by optimizing the longitudinal magnetic field in the discharge chamber. While this project demonstrated the advantages of the pulsed version of the SA RF SPS as an upgrade to the ORNL Spallation Neutron Source, it led to a possibility for upgrades to CW machines like the many cyclotrons used for commercial applications. Four appendices contain important details of the work carried out under this grant.

  9. Interaction of relativistic H- ions with thin foils

    International Nuclear Information System (INIS)

    Mohagheghi, A.H.

    1990-09-01

    The response of relativistic H - ions to thin carbon foils was investigated for beam energies ranging from 226 MeV to 800 MeV. For the foil thicknesses we have studied, ranging from 15 to 300 μg/cm 2 , an appreciable fraction of the H - beam survives intact, some H - ions are stripped down to protons, and the remainder is distributed over the states of H 0 . This experiment is different from the low energy studies in that the projectile velocity is comparable to the speed of light, leading to an interaction time of typically less than a femtosecond. The present results challenge the theoretical understanding of the interaction mechanisms. An electron spectrometer was used to selectively field-ionize the Rydberg states, 9 < n < 17, at beam energies of 581 MeV and 800 MeV. The yield of low-lying states were measured by Doppler tuning a Nd:YAG laser to excite transitions to a Rydberg state which was then field-ionized and detected. A simple model is developed to fit the yield of each state as a function of foil thickness. The simple model is successful in predicting the general features of the yield data. However, the data are suggestive of a more complex structure in the yield curves. The yield of a given state depends strongly on the foil thickness, demonstrating that the excited states are formed during the passage of the ions through a foil. The optimum thickness to produce a given state increases with the principal quantum number of the state suggesting an excitation process which is at least pratially stepwise. The results of a Monte Carlo simulation are compared with the experimental data to estimate the distribution of the excited states coming out of a foil. The distributions of the excited states and their dependence on foil thickness are discussed

  10. Autopilot regulation for the Linac4 H- ion source

    Science.gov (United States)

    Voulgarakis, G.; Lettry, J.; Mattei, S.; Lefort, B.; Costa, V. J. Correia

    2017-08-01

    Linac4 is a 160 MeV H- linear accelerator part of the upgrade of the LHC injector chain. Its cesiated surface H- source is designed to provide a beam intensity of 40-50mA. It is operated with periodical Cs-injection at typically 30 days intervals [1] and this implies that the beam parameters will slowly evolve during operation. Autopilot is a control software package extending CERN developed Inspector framework. The aim of Autopilot is to automatize the mandatory optimization and cesiation processes and to derive performance indicators, thus keeping human intervention minimal. Autopilot has been developed by capitalizing on the experience from manually operating the source. It comprises various algorithms running in real-time, which have been devised to: • Optimize the ion source performance by regulation of H2 injection, RF power and frequency. • Describe the performance of the source with performance indicators, which can be easily understood by operators. • Identify failures, try to recover the nominal operation and send warning in case of deviation from nominal operation. • Make the performance indicators remotely available through Web pages.Autopilot is at the same level of hierarchy as an operator, in the CERN infrastructure. This allows the combination of all ion source devices, providing the required flexibility. Autopilot is executed in a dedicated server, ensuring unique and centralized control, yet allowing multiple operators to interact at runtime, always coordinating between them. Autopilot aims at flexibility, adaptability, portability and scalability, and can be extended to other components of CERN's accelerators. In this paper, a detailed description of the Autopilot algorithms is presented, along with first results of operating the Linac4 H- Ion Source with Autopilot.

  11. Coupled Ca2+/H+ transport by cytoplasmic buffers regulates local Ca2+ and H+ ion signaling.

    Science.gov (United States)

    Swietach, Pawel; Youm, Jae-Boum; Saegusa, Noriko; Leem, Chae-Hun; Spitzer, Kenneth W; Vaughan-Jones, Richard D

    2013-05-28

    Ca(2+) signaling regulates cell function. This is subject to modulation by H(+) ions that are universal end-products of metabolism. Due to slow diffusion and common buffers, changes in cytoplasmic [Ca(2+)] ([Ca(2+)]i) or [H(+)] ([H(+)]i) can become compartmentalized, leading potentially to complex spatial Ca(2+)/H(+) coupling. This was studied by fluorescence imaging of cardiac myocytes. An increase in [H(+)]i, produced by superfusion of acetate (salt of membrane-permeant weak acid), evoked a [Ca(2+)]i rise, independent of sarcolemmal Ca(2+) influx or release from mitochondria, sarcoplasmic reticulum, or acidic stores. Photolytic H(+) uncaging from 2-nitrobenzaldehyde also raised [Ca(2+)]i, and the yield was reduced following inhibition of glycolysis or mitochondrial respiration. H(+) uncaging into buffer mixtures in vitro demonstrated that Ca(2+) unloading from proteins, histidyl dipeptides (HDPs; e.g., carnosine), and ATP can underlie the H(+)-evoked [Ca(2+)]i rise. Raising [H(+)]i tonically at one end of a myocyte evoked a local [Ca(2+)]i rise in the acidic microdomain, which did not dissipate. The result is consistent with uphill Ca(2+) transport into the acidic zone via Ca(2+)/H(+) exchange on diffusible HDPs and ATP molecules, energized by the [H(+)]i gradient. Ca(2+) recruitment to a localized acid microdomain was greatly reduced during intracellular Mg(2+) overload or by ATP depletion, maneuvers that reduce the Ca(2+)-carrying capacity of HDPs. Cytoplasmic HDPs and ATP underlie spatial Ca(2+)/H(+) coupling in the cardiac myocyte by providing ion exchange and transport on common buffer sites. Given the abundance of cellular HDPs and ATP, spatial Ca(2+)/H(+) coupling is likely to be of general importance in cell signaling.

  12. Experiments of an intense H{sup -} ion beam acceleration

    Energy Technology Data Exchange (ETDEWEB)

    Ando, A.; Takeiri, Y.; Kaneko, O.; Oka, Y.; Tsumori, K.; Asano, E.; Kawamoto, T.; Akiyama, R.; Kuroda, T.

    1995-08-01

    An intense H{sup -} beam of a single beamlet is extracted from a large multicusp plasma source operated with cesium seeding. The H{sup -} beams are accelerated up to 100keV by a single-stage or a two-stage electrode system. Spatial profiles of the beams are measured calorimetrically and a minimum beam divergence angle of 5mrad is achieved at a H{sup -} current density of 30mA/cm{sup 2} with a beam energy of 100keV. A ratio of an acceleration current to a H{sup -} current increases abruptly when a H{sup -} current saturates in the space charge limited region. This enhancement is mainly due to secondary electrons caused by the intersection of H{sup -} beams with an extraction grid. When an operating gas pressure decreases, the ratio of the acceleration current to the H{sup -} current decreases. This is related to a stripping loss of H{sup -} ions in the electrodes. A beam divergence angle becomes minimum when a ratio of V{sub acc} to V{sub ext} is set at a optimum value of 1.6 in the single-stage acceleration. This ratio is almost the same as that in the double-stage acceleration, where the optimum ratio of E{sub acc1}/E{sub ext} is 1.5. In the optimum E{sub acc1}/E{sub ext} ratio the divergence angle is not affected by V{sub acc2}. The divergence angle can be reduced by changing V{sub acc2} even if the ratio of E{sub acc1}/E{sub ext} is not optimized. The beam steering effect by permanent magnets buried in an extraction grid is observed in nine beamlets experiments. A simple calculation of a single particle trajectory gives a good approximation of the beam deflection angle. (author).

  13. A compact rf driven H- ion source for linac injection

    International Nuclear Information System (INIS)

    Rymer, J.P.; Engeman, G.A.; Hamm, R.W.; Potter, J.M.

    1991-01-01

    A compact rf driven H - ion source has been developed for use as an injector for the AccSys radio frequency quadrupole (RFQ) linacs. A multicusp magnetic bucket geometry developed at Lawrence Berkeley Laboratory confines the plasma created by an antenna driven by 35 kW (peak) of pulsed rf power at 1.8 MHz. A three electrode system is used to extract and accelerate the H - beam, which is then focused into the RFQ by an einzel lens. Permanent magnets in the extraction region sweep electrons onto the second electrode at energies up to half of the full acceleration voltage. A fast pulsed valve allows the hydrogen gas supply to be pulsed, thus minimizing the average gas flow rate into the system. The design features and performance data from the prototype are discussed

  14. The HeH+ molecular ion in a magnetic field

    International Nuclear Information System (INIS)

    Turbiner, A V; Guevara, N L

    2007-01-01

    A detailed study of the low-lying electronic states 1 Σ, 3 Σ, 3 Π, 3 Δ of the HeH + molecular ion in parallel to a magnetic field configuration (when α-particle and proton are situated on the same magnetic line) is carried out for B = 0 - 4.414 x 10 13 G in the Born-Oppenheimer approximation. The variational method is employed using a physically adequate trial function. It is shown that for the Σ states the parallel configuration is stable with respect to small deviations. The quantum numbers of the ground state depend on the magnetic field strength. The ground state evolves from the spin-singlet 1 Σ state for small magnetic fields B ∼ 3 Σ (unbound or weakly bound) state for intermediate fields and to the spin-triplet strongly bound 3 Π state for B ∼> 15 au. When the HeH + molecular ion exists, it is stable with respect to dissociation

  15. Status of the ITER Ion Cyclotron H&CD

    Directory of Open Access Journals (Sweden)

    Beaumont Bertrand

    2017-01-01

    Full Text Available The ITER Ion Cyclotron Heating and Current Drive system (IC H&CD is designed to deliver 20MW to a broad range of plasma scenarios between 40 and 55MHz, during very long pulses. It consists of two broadband equatorial port plug antennas, their pre-matching and matching systems, transmission lines, Radio Frequency (RF Sources and High Voltage Power Supplies. The overall project schedule has been revised and agreed by ITER Council; it re-integrates the second antenna and its power supplies in construction baseline and sets the dates for progressive installation with DT phase planned in 2035. Recent progress on ICRF subsystems is reported, covering design evolution, qualification of test articles and specific R&D results in domestic agencies, suppliers, associated laboratories and IO.

  16. Bis(sulfonamide) transmembrane carriers allow pH-gated inversion of ion selectivity.

    Science.gov (United States)

    Roy, Arundhati; Biswas, Oindrila; Talukdar, Pinaki

    2017-03-09

    Bis(sulfonamide) based synthetic carriers are reported for inversion of ion selectivity upon deviation of pH within a narrow window. A liposomal membrane potential is also generated when potassium ions are passively transported by these carriers.

  17. Multi-ion and pH sensitivity of AgGeSe ion selective electrodes

    Science.gov (United States)

    Conde Garrido, J. M.; Silveyra, J. M.; Ureña, M. A.

    2016-02-01

    Many chalcogenide glasses have been found to combine benefits such as good chemical durability, selectivity, and reproducibility for applications as solid-state sensitive membranes of ion selective electrodes (ISEs). In previous works, we have shown that ISEs with ionic conductive AgGeSe membranes have good sensitivity to Ag+ ions. In the present work, we explore the Agx(Ge0.25Se0.75)100-x, 10≤x≤30 (at%) system as candidate for ISEs applications detecting several other ions (K+, Mg2+, Cr3+, Fe3+, Ni2+, Cd2+, Hg2+, and Pb2+). We evaluated ISEs fabricated with bulk as well as with thin film membranes. We found no dependence of the sensing properties on the Ag content of the ionic conductive membranes. Thin films exhibited the same properties than bulk membranes, indicating that these chalcogenide glasses have great potential for miniaturization. The ISEs showed a high response (Nernstian or super-Nernstian) to the presence of Hg2+, Pb2+, and Fe3+, a low response (sub-Nernstian) to the presence of Cr3+, and a total lack of response to the presence of Cd2+, Ni2+, Mg2+, and K+. We also tested how the pH of the solution affected the response of the ISEs. The potentials of the ISEs were practically constant in neutral or acidic solutions, while decreased drastically in basic solutions when the primary ion was not present. The latter phenomenon was caused by the slow dissolution of the membrane into the solution, meaning that long-term basic environments should be avoided for these ISEs. We concluded that ISEs with ionic conductive AgGeSe membranes are good candidates to integrate multi-electrode systems.

  18. Continued fractions and the hydrogen molecular ion H2+

    Science.gov (United States)

    Nickel, Bernie

    2011-09-01

    The Jaffé continued fraction solution for the hydrogen molecular ion has been the basis for most H2+ energy calculations at physically relevant nuclear separation R. I show that its slow convergence at small R can be overcome so it can also be used to obtain the power series expansion of the energy about the united atom limit R = 0. I restrict the discussion to the H2+ ground state and show, by a generalization of Wynn's accelerated convergence technique and an analytical calculation, that the continued fraction yields the O(R5) series term which is the first term in which log(R) makes an appearance. For higher order terms I apply the convergence method numerically to obtain very accurate energies at small R and, by fitting, numerical coefficients in the R series. The analytic representations of the coefficients are identified using the integer relation algorithm PSLQ. All terms to O(R14) are obtained exactly and to O(R20) in a mixed analytic/numeric form. Comparisons with previous work based on wavefunction perturbation theory are made.

  19. Continued fractions and the hydrogen molecular ion H2+

    International Nuclear Information System (INIS)

    Nickel, Bernie

    2011-01-01

    The Jaffe continued fraction solution for the hydrogen molecular ion has been the basis for most H 2 + energy calculations at physically relevant nuclear separation R. I show that its slow convergence at small R can be overcome so it can also be used to obtain the power series expansion of the energy about the united atom limit R = 0. I restrict the discussion to the H 2 + ground state and show, by a generalization of Wynn's accelerated convergence technique and an analytical calculation, that the continued fraction yields the O(R 5 ) series term which is the first term in which log(R) makes an appearance. For higher order terms I apply the convergence method numerically to obtain very accurate energies at small R and, by fitting, numerical coefficients in the R series. The analytic representations of the coefficients are identified using the integer relation algorithm PSLQ. All terms to O(R 14 ) are obtained exactly and to O(R 20 ) in a mixed analytic/numeric form. Comparisons with previous work based on wavefunction perturbation theory are made. (paper)

  20. Status of the ITER Ion Cyclotron H and CD system

    Energy Technology Data Exchange (ETDEWEB)

    Lamalle, P., E-mail: philippe.lamalle@iter.org [ITER Organization, Route de Vinon sur Verdon, 13115 St Paul-lez-Durance (France); Beaumont, B.; Kazarian, F.; Gassmann, T. [ITER Organization, Route de Vinon sur Verdon, 13115 St Paul-lez-Durance (France); Agarici, G. [Fusion for Energy, Carrer Josep Pla 2, Torres Diagonal Litoral Edificio B3, 08019 Barcelona (Spain); Ajesh, P. [ITER India, Institute for Plasma Research, Bhat, Gandhinagar 382424, Gujarat (India); Alonzo, T. [Solution F, Allée du Verdon, 13770 Venelles (France); Arambhadiya, B. [ITER Organization, Route de Vinon sur Verdon, 13115 St Paul-lez-Durance (France); Argouarch, A. [CEA Cadarache, IRFM, F-13108 St-Paul-lez-Durance (France); Bamber, R. [EURATOM/CCFE Association, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Berger-By, G.; Bernard, J.-M.; Brun, C. [CEA Cadarache, IRFM, F-13108 St-Paul-lez-Durance (France); Carpentier, S. [ITER Organization, Route de Vinon sur Verdon, 13115 St Paul-lez-Durance (France); Clairet, F.; Colas, L.; Courtois, X. [CEA Cadarache, IRFM, F-13108 St-Paul-lez-Durance (France); Davis, A. [EURATOM/CCFE Association, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Dechelle, C.; Doceul, L. [CEA Cadarache, IRFM, F-13108 St-Paul-lez-Durance (France); and others

    2013-10-15

    Highlights: ► We summarize the progress and outstanding issues in the development of the ITER Ion Cyclotron Heating and Current Drive (IC H and CD) system. ► The system is designed to robustly couple 20 MW in quasi-CW operation for a broad range of plasma scenarios, and is upgradeable to up to 40 MW. ► The design is rendered challenging by the wide spectrum of requirements and interface constraints to which it is subject. ► R and D is ongoing to validate key antenna components, and to qualify the radio-frequency (RF) sources and the transmission and matching components. ► Intensive numerical modeling and experimental studies on antenna mock-ups have been conducted to validate and optimize the RF design. -- Abstract: The ongoing design of the ITER Ion Cyclotron Heating and Current Drive system (20 MW, 40–55 MHz) is rendered challenging by the wide spectrum of requirements and interface constraints to which it is subject, several of which are conflicting and/or still in a high state of flux. These requirements include operation over a broad range of plasma scenarios and magnetic fields (which prompts usage of wide-band phased antenna arrays), high radio-frequency (RF) power density at the first wall (and associated operation close to voltage and current limits), resilience to ELM-induced load variations, intense thermal and mechanical loads, long pulse operation, high system availability, efficient nuclear shielding, high density of antenna services, remote-handling ability, tight installation tolerances, and nuclear safety function as tritium confinement barrier. R and D activities are ongoing or in preparation to validate critical antenna components (plasma-facing Faraday screen, RF sliding contacts, RF vacuum windows), as well as to qualify the RF power sources and the transmission and matching components. Intensive numerical modeling and experimental studies on antenna mock-ups have been conducted to validate and optimize the RF design. The paper

  1. Large scale silver nanowires network fabricated by MeV hydrogen (H+) ion beam irradiation

    International Nuclear Information System (INIS)

    S, Honey; S, Naseem; A, Ishaq; M, Maaza; M T, Bhatti; D, Wan

    2016-01-01

    A random two-dimensional large scale nano-network of silver nanowires (Ag-NWs) is fabricated by MeV hydrogen (H + ) ion beam irradiation. Ag-NWs are irradiated under H +  ion beam at different ion fluences at room temperature. The Ag-NW network is fabricated by H + ion beam-induced welding of Ag-NWs at intersecting positions. H +  ion beam induced welding is confirmed by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). Moreover, the structure of Ag NWs remains stable under H +  ion beam, and networks are optically transparent. Morphology also remains stable under H +  ion beam irradiation. No slicings or cuttings of Ag-NWs are observed under MeV H +  ion beam irradiation. The results exhibit that the formation of Ag-NW network proceeds through three steps: ion beam induced thermal spikes lead to the local heating of Ag-NWs, the formation of simple junctions on small scale, and the formation of a large scale network. This observation is useful for using Ag-NWs based devices in upper space where protons are abandoned in an energy range from MeV to GeV. This high-quality Ag-NW network can also be used as a transparent electrode for optoelectronics devices. (paper)

  2. Effect of pH, various divalent metal ion and different substrates on ...

    African Journals Online (AJOL)

    EZUGWU ARINZE LINUS

    Key words: Glucoamylase, pH, metal ions, Aspergillus niger, tiger nut starch, amylopectin. INTRODUCTION. Glucoamylase (α-1 ... glycosidic bonds from the non-reducing ends of starch and 1,6-alpha-glucsidic linkages in ..... stable at neutral pH 7.0, it is more likely to readily form neucleophilichydroxide ions with metals by ...

  3. A 100 keV operation of a large vacuum-immersed H - ion source

    Science.gov (United States)

    Oka, Y.; Kaneko, O.; Takeiri, Y.; Tsumori, K.; Ando, A.; Asano, E.; Akiyama, R.; Kawamoto, T.; Kuroda, T.

    1996-03-01

    A large vacuum-immersed H- ion source has been operated on the negative-ion-based neutral beam teststand. The achieved level of the beam and the pulse duration in beam conditioning were limited by a high-voltage breakdown in the vacuum vessel. A baffle plate at grounded potential for shielding completely from the charged particles was successful. A beam with an energy of up to 102 keV and the H- ion current of 0.55 A were achieved for 0.29 s without the breakdown. The ion current of ˜1.5 A was accelerated in cesium-seeded operation. The corresponding ion current density was ˜7 mA/cm2. A magnetic filter (as Type I LV magnetic filter) on the plasma electrode was applied. The electron beam component which was extracted from the plasma source together with H- ions was found to be very reduced.

  4. Present status of the Rutherford and Appleton Laboratories' H- ion source

    International Nuclear Information System (INIS)

    Gear, P.E.; Sidlow, R.

    1981-07-01

    A surface conversion ion source of the Penning type is being developed at the Rutherford and Appleton Laboratories for use with the pulsed spallation neutron source (SNS) currently under construction. The ion source is required to deliver 40 mA of H - ions at a duty factor of 2.5% (50 Hz x 500 μsec). At the present time 30 mA of H - ions have been extracted with the source operating at a duty factor of 2.1%. (author)

  5. Rotational state resolved photodissociation spectroscopy of translationally and vibrationally cold MgH+ ions: toward rotational cooling of molecular ions

    DEFF Research Database (Denmark)

    Højbjerre, Klaus; Hansen, Anders Kragh; Skyt, Peter Sandegaard

    2009-01-01

    and vibrationally cold MgH+ ions are presented, with and without the optical pumping laser being present. While rotational cooling is as yet not evident, first results showed evidence of a change in the rotational distribution in the presence of the optical pumping laser.......The first steps toward the implementation of a simple scheme for rotational cooling of MgH+ ions based on rotational state optical pumping is considered. The various aspects of such an experiment are described in detail, and the rotational state-selective dissociation spectra of translationally...

  6. Warm-ion drift Alfven turbulence and the L-H transition

    International Nuclear Information System (INIS)

    Scott, B.

    1998-01-01

    Computations of fluid drift turbulence treating ions and electrons on equal footing, including both temperatures, are conducted in a model toroidal geometry. The resulting 'ion mixing mode' turbulence bears features of both electron drift-Alfven and ion temperature gradient turbulence, and nonlinear sensitivity to the relative strengths of the density and temperature gradients provides a possible route to the bifurcation needed for the L-H transition. (author)

  7. Recent operating experience with the H- ion injector at LAMPF/LANSCE

    International Nuclear Information System (INIS)

    Ingalls, W.B.; Stelzer, J.E.; Williams, H.E. III.

    1996-01-01

    A cusp-field cesium conversion ion source has provided H - beams at LAMPF/LANSCE since 1984. three interchangeable sources are now used during beam production cycles to minimize down time during scheduled source change-outs. Ion source change-outs are scheduled to prevent unscheduled loss of beam time due to finite filament lifetime. Ion source operating parameters and filament lifetime data are presented

  8. CW/Pulsed H- ion beam generation with PKU Cs-free 2.45 GHz microwave driven ion source

    Science.gov (United States)

    Peng, S. X.; Ren, H. T.; Xu, Y.; Zhang, T.; Zhang, A. L.; Zhang, J. F.; Zhao, J.; Guo, Z. Y.; Chen, J. E.

    2015-04-01

    Circular accelerators used for positron emission tomography (PET, i.e. accelerator used for make radio isotopes) need several mA of CW H- ion beam for their routine operation. Other facilities, like Space Radio-Environment Simulate Assembly (SPRESA), require less than 10 mA pulsed mode H- beam. Caesium free negative hydrogen ion source is a good choice for those facilities because of its compact structure, easy operation and low cost. Up to now, there is no H- source able to produce very intense H- beams with important variation of the duty factor[1]. Recently, a new version of 2.45 GHz microwave H- ion source was designed at PKU, based on lessons learnt from the previous one. This non cesiated source is very compact thanks to its permanent magnet configuration. Special attention was paid on the design of the discharge chamber structure, electron dumping and extraction system. Source test to produce H- ion beams in pulsed and CW mode was carried out on PKU ion source test bench. In CW mode, a 10.8 mA/30keV H- beam with rms emittance about 0.16 π.mm.mrad has been obtained with only 500 W rf power. The power efficiency reaches 21 mA/kW. In pulsed mode with duty factor of 10% (100Hz/1ms), this compact source can easily deliver 20 mA H- ion beam at 35 keV with rms emittance about 0.2 π.mm.mrad when RF power is set at 2.2 kW (peak power). Several hour successive running operation in both modes and totaling more than 200 hours proves its high quality. The outside dimension of this new H- source body is ϕ116 mm × 124 mm, and the entire H- source infrastructure, including rf matching section, plasma chamber and extraction system, is ϕ310 × 180 mm. The high voltage region is limited with in a ϕ310 mm × 230 mm diagram. Details are given in this paper.

  9. The Effects of Hydrogen Band EMIC Waves on Ring Current H+ Ions

    Science.gov (United States)

    Wang, Zhiqiang; Zhai, Hao; Gao, Zhuxiu

    2017-12-01

    Hydrogen band electromagnetic ion cyclotron (EMIC) waves have received much attention recently because they are found to frequently span larger spatial areas than the other band EMIC waves. Using test particle simulations, we study the nonlinear effects of hydrogen band EMIC waves on ring current H+ ions. A dimensionless parameter R is used to characterize the competition between wave-induced and adiabatic motions. The results indicate that there are three regimes of wave-particle interactions for typical 35 keV H+ ions at L = 5: diffusive (quasi-linear) behavior when αeq ≤ 35° (R ≥ 2.45), the nonlinear phase trapping when 35° < αeq < 50° (0.75 < R < 2.45), and both the nonlinear phase bunching and phase trapping when αeq ≥ 50° (R ≤ 0.75). The phase trapping can transport H+ ions toward large pitch angle, while the phase bunching has the opposite effect. The phase-trapped H+ ions can be significantly accelerated (from 35 keV to over 500 keV) in about 4 min and thus contribute to the formation of high energy components of ring current ions. The results suggest that the effect of hydrogen band EMIC waves is not ignorable in the nonlinear acceleration and resonance scattering of ring current H+ ions.

  10. Ion thermal conductivity and convective energy transport in JET hot-ion regimes and H-modes

    International Nuclear Information System (INIS)

    Tibone, F.; Balet, B.; Cordey, J.G.

    1989-01-01

    Local transport in a recent series of JET experiments has been studied using interpretive codes. Auxiliary heating, mainly via neutral beam injection, was applied on low-density target plasmas confined in the double-null X-point configuration. This has produced two-component plasmas with high ion temperature and neutron yield and, above a threshold density, H-modes characterised by peak density and power deposition profiles. H-mode confinement was also obtained for the first time with 25 MW auxiliary power, of which 10 MW was from ion cyclotron resonance heating. We have used profile measurements of electron temperature T e from electron cyclotron emission and LIDAR Thomson scattering, ion temperature T i from charge-exchange recombination spectroscopy (during NBI), electron density n e from LIDAR and Abel-inverted interferometer measurements. Only sparse information is, however, available to date concerning radial profiles of effective ionic charge and radiation losses. Deuterium depletion due to high impurity levels is an important effect in these discharges, and our interpretation of thermal ion energy content, neutron yield and ion particle fluxes needs to be confirmed using measured Z eff -profiles. (author) 4 refs., 4 figs

  11. pH- and ion-sensitive polymers for drug delivery.

    Science.gov (United States)

    Yoshida, Takayuki; Lai, Tsz Chung; Kwon, Glen S; Sako, Kazuhiro

    2013-11-01

    Drug delivery systems (DDSs) are important for effective, safe, and convenient administration of drugs. pH- and ion-responsive polymers have been widely employed in DDS for site-specific drug release due to their abilities to exploit specific pH- or ion-gradients in the human body. Having pH-sensitivity, cationic polymers can mask the taste of drugs and release drugs in the stomach by responding to gastric low pH. Anionic polymers responsive to intestinal high pH are used for preventing gastric degradation of drug, colon drug delivery and achieving high bioavailability of weak basic drugs. Tumor-targeted DDSs have been developed based on polymers with imidazole groups or poly(β-amino ester) responsive to tumoral low pH. Polymers with pH-sensitive chemical linkages, such as hydrazone, acetal, ortho ester and vinyl ester, pH-sensitive cell-penetrating peptides and cationic polymers undergoing pH-dependent protonation have been studied to utilize the pH gradient along the endocytic pathway for intracellular drug delivery. As ion-sensitive polymers, ion-exchange resins are frequently used for taste-masking, counterion-responsive drug release and sustained drug release. Polymers responding to ions in the saliva and gastrointestinal fluids are also used for controlled drug release in oral drug formulations. Stimuli-responsive DDSs are important for achieving site-specific and controlled drug release; however, intraindividual, interindividual and intercellular variations of pH should be considered when designing DDSs or drug products. Combination of polymers and other components, and deeper understanding of human physiology are important for development of pH- and ion-sensitive polymeric DDS products for patients.

  12. pH- and ion-sensitive polymers for drug delivery

    Science.gov (United States)

    Yoshida, Takayuki; Lai, Tsz Chung; Kwon, Glen S; Sako, Kazuhiro

    2013-01-01

    Introduction Drug delivery systems (DDSs) are important for effective, safe, and convenient administration of drugs. pH- and ion-responsive polymers have been widely employed in DDS for site-specific drug release due to their abilities to exploit specific pH- or ion-gradients in the human body. Areas covered Having pH-sensitivity, cationic polymers can mask the taste of drugs and release drugs in the stomach by responding to gastric low pH. Anionic polymers responsive to intestinal high pH are used for preventing gastric degradation of drug, colon drug delivery and achieving high bioavailability of weak basic drugs. Tumor-targeted DDSs have been developed based on polymers with imidazole groups or poly(β-amino ester) responsive to tumoral low pH. Polymers with pH-sensitive chemical linkages, such as hydrazone, acetal, ortho ester and vinyl ester, pH-sensitive cell-penetrating peptides and cationic polymers undergoing pH-dependent protonation have been studied to utilize the pH gradient along the endocytic pathway for intracellular drug delivery. As ion-sensitive polymers, ion-exchange resins are frequently used for taste-masking, counterion-responsive drug release and sustained drug release. Polymers responding to ions in the saliva and gastrointestinal fluids are also used for controlled drug release in oral drug formulations. Expert opinion Stimuli-responsive DDSs are important for achieving site-specific and controlled drug release; however, intraindividual, interindividual and intercellular variations of pH should be considered when designing DDSs or drug products. Combination of polymers and other components, and deeper understanding of human physiology are important for development of pH- and ion-sensitive polymeric DDS products for patients. PMID:23930949

  13. Recombination of KrD+ and KrH+ ions in afterglow plasma

    International Nuclear Information System (INIS)

    Korolov, I; Kotrik, T; Plasil, R; Hejduk, M; Varju, J; Dohnal, P; Glosik, J

    2009-01-01

    Reported is flowing afterglow (FALP) study of recombination of KrH + and KrD + ions with electrons at 250 K in mixtures of He/Kr/H 2 and He/Kr/D 2 , respectively. The influence of fast recombining cluster ions formation on apparent effective recombination rate coefficients (α eff ) was measured and used in data analysis. The obtained binary rate coefficients for recombination of KrH + and KrD + are α KrH+ = 2x10 -8 cm 3 s -1 and α KrD+ = 1x10 -8 cm 3 s -1 .

  14. Recombination of KrD+ and KrH+ ions in afterglow plasma

    Science.gov (United States)

    Korolov, I.; Kotrik, T.; Plasil, R.; Hejduk, M.; Varju, J.; Dohnal, P.; Glosik, J.

    2009-11-01

    Reported is flowing afterglow (FALP) study of recombination of KrH+ and KrD+ ions with electrons at 250 K in mixtures of He/Kr/H2 and He/Kr/D2, respectively. The influence of fast recombining cluster ions formation on apparent effective recombination rate coefficients (αeff) was measured and used in data analysis. The obtained binary rate coefficients for recombination of KrH+ and KrD+ are αKrH+ = 2×10-8 cm3s-1 and αKrD+ = 1×10-8 cm3s-1.

  15. Generation of H-, H2(v double-prime), and H atoms by H2+ and H3+ ions incident upon barium surfaces

    International Nuclear Information System (INIS)

    Hiskes, J.R.; Karo, A.M.

    1989-01-01

    The generation of vibrationally excited molecules by electron excitation collisions and the subsequent generation of negative ions by dissociative attachment to these molecules has become a standard model for volume source operation. These processes have been supplemented recently by the demonstration of atom-surface recombination to form vibrationally excited molecules, and enhanced negative ion formation by protons incident upon barium electrodes. In this paper we consider the additional processes of molecular vibrational excitation generated by recombination of molecular ions on the electrode surfaces, and negative ion formation by vibrationally excited molecules rebounding from low work-function electrodes. 10 refs., 4 figs

  16. Sodium ions as substitutes for protons in the gastric H,K-ATPase

    International Nuclear Information System (INIS)

    Polvani, C.; Sachs, G.; Blostein, R.

    1989-01-01

    In view of the striking homology among various ion-translocating ATPases including Na,K-ATPase, Ca-ATPase, and H,K-ATPase, and the recent evidence that protons can replace cytoplasmic sodium as well as potassium in the reaction mechanism of the Na,K-ATPase (Polvani, C., and Blostein, R. (1988) J. Biol. Chem. 263, 16757-16763), we studied the role of sodium as a substitute for protons in the H,K-ATPase reaction. Using hog gastric H,K-ATPase-rich inside-out membrane vesicles we observed 22Na+ influx which was stimulated by intravesicular potassium ions (K+i) at pH 8.5 but not at pH 7.1. This sodium influx was observed in medium containing ATP and was inhibited by vanadate and SCH28080, a selective inhibitor of the gastric H,K-ATPase. At least 2-fold accumulation of sodium was observed at pH 8.5. Experiments aimed to determine the sidedness of the alkaline pH requirement for K+i-dependent sodium influx showed that K+i-activated sodium influx depends on pHout and is unaffected by changes in pHin. These results support the conclusion that sodium ions substitute for protons in the H,K-ATPase reaction mechanism and provide evidence for a similarity in ion selectivity and/or binding domains of the Na,K-ATPase and the gastric H,K-ATPase enzymes

  17. Ion transport and selectivity in biomimetic nanopores with pH-tunable zwitterionic polyelectrolyte brushes

    Science.gov (United States)

    Zeng, Zhenping; Yeh, Li-Hsien; Zhang, Mingkan; Qian, Shizhi

    2015-10-01

    Inspired by nature, functionalized nanopores with biomimetic structures have attracted growing interests in using them as novel platforms for applications of regulating ion and nanoparticle transport. To improve these emerging applications, we study theoretically for the first time the ion transport and selectivity in short nanopores functionalized with pH tunable, zwitterionic polyelectrolyte (PE) brushes. In addition to background salt ions, the study takes into account the presence of H+ and OH- ions along with the chemistry reactions between functional groups on PE chains and protons. Due to ion concentration polarization, the charge density of PE layers is not homogeneously distributed and depends significantly on the background salt concentration, pH, grafting density of PE chains, and applied voltage bias, thereby resulting in many interesting and unexpected ion transport phenomena in the nanopore. For example, the ion selectivity of the biomimetic nanopore can be regulated from anion-selective (cation-selective) to cation-selective (anion-selective) by diminishing (raising) the solution pH when a sufficiently small grafting density of PE chains, large voltage bias, and low background salt concentration are applied.

  18. Spectroscopic measurements of an H- ion source discharge

    International Nuclear Information System (INIS)

    Keller, R.; Smith, H.V. Jr.

    1985-01-01

    Spectral emission lines from an H - Penning surface-plasma source (SPS), the 4X source, are examined in the visible and near ultraviolet. Electron distribution temperatures are deduced from integral line-strength measurements. These temperatures are surprisingly low, about 0.5 eV. Electron density values of about 1.5 x 10 14 cm -3 and H-atom energies between 2 and 2.6 eV are determined from the measured Balmer-line profiles. Assuming the H - energy is identical to the H-atom energy, an emittance limit of 0.006 π x cm x mrad is deduced for this source with a 5.4-mm aperture

  19. Molecular treatment of the ion-pair formation reaction in H(1s) + H(1s) collisions

    Energy Technology Data Exchange (ETDEWEB)

    Borondo, F.; Martin, F.; Yaez, M.

    1987-01-01

    All the available theoretical calculations of the cross section for the ion-pair formation reaction H(1s)+H(1s)..-->..H/sup +/H/sup -/(1s/sup 2/) have been performed using methods that are only valid at high collision energies. They get good agreement with the experiments for impact energies greater than 25 keV, but fail completely at smaller energies. In this work we report the cross section for this reaction at impact energies less than 10 keV, calculated in the framework of the impact-parameter approximation and using the molecular method with a common translation factor.

  20. Orientation and impact-parameter dependence of dissociative ionization of H2 by slow ion impact

    International Nuclear Information System (INIS)

    Afaneh, F; Schmidt, L Ph H; Schoeffler, M; Stiebing, K E; Al-Jundi, J; Schmidt-Boecking, H; Doerner, R

    2007-01-01

    We have used the cold target recoil ion momentum spectroscopy imaging technique to investigate dissociative ionization of H 2 by 25 keV proton impact. A kinematically complete picture of the dissociative ionization dynamics for slow proton collision has been obtained. The results show a strong impact-parameter dependence of the fragmentation process of H 2 . This clearly emerged in the energy distributions of the H + ions generated for different impact parameters. At large impact parameters the H + ions equally share the energy liberated in the collision whereas at small impact parameters, the energy sharing is quite asymmetric. We also observed a strong dependence of the electron emission on molecular alignment. The momentum distribution of the emitted electron generated for a fixed-in-space H 2 molecule displays that the electrons are more likely to be emitted perpendicular to the molecular axis

  1. 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.

  2. A study of strengthening mechanism for high energy titanium ion implantation into H13 steel

    International Nuclear Information System (INIS)

    Zhang Tonghe; Chen Jun

    1995-05-01

    The strengthening mechanism of high energy titanium ion implanted H13 steel was studied. The results shown that several kinds of strengthening factors played a part in strengthening together when the high energy titanium ions were implanted into H13 steel. The solution strengthening and dislocation strengthening were dominated if Ti ions were implanted with high dose at low temperature. The strengthening effects were increased. The Fe 2 Ti and TiC phases were formed in H13 steel when the Ti ions were implanted with high dose at 400 degree C. The dispersion strengthening phases of Fe 2 Ti and TiC were appeared. The strengthening effects are better than before. The hardness increased 3.2 times, the wear resistance increased 11 times. (2 tabs., 7 figs.)

  3. Experimental ion mobility measurements in Xe-C2H6

    Science.gov (United States)

    Perdigoto, J. M. C.; Cortez, A. F. V.; Veenhof, R.; Neves, P. N. B.; Santos, F. P.; Borges, F. I. G. M.; Conde, C. A. N.

    2017-10-01

    In this paper we present the results of the ion mobility measurements made in gaseous mixtures of xenon (Xe) with ethane (C2H6) for pressures ranging from 6 to 10 Torr (8-10.6 mbar) and for low reduced electric fields in the 10 Td to 25 Td range (2.4-6.1 kVṡcm-1ṡ bar-1), at room temperature. The time of arrival spectra revealed two peaks throughout the entire range studied which were attributed to ion species with 3-carbons (C3H5+, C3H6+ C3H8+ and C3H9+) and with 4-carbons (C4H7+, C4H9+ and C4H10+). Besides these, and for Xe concentrations above 70%, a bump starts to appear at the right side of the main peak for reduced electric fields higher than 20 Td, which was attributed to the resonant charge transfer of C2H6+ to C2H6 that affects the mobility of its ion products (C3H8+ and C3H9+). The time of arrival spectra for Xe concentrations of 20%, 50%, 70% and 90% are presented, together with the reduced mobilities as a function of the Xe concentration calculated from the peaks observed for the low reduced electric fields and pressures studied.

  4. Experimental ion mobility measurements in Xe-C2H6

    International Nuclear Information System (INIS)

    Perdigoto, J.M.C.; Cortez, A.F.V.; Santos, F.P.; Borges, F.I.G.M.; Conde, C.A.N.; Veenhof, R.; Neves, P.N.B.

    2017-01-01

    In this paper we present the results of the ion mobility measurements made in gaseous mixtures of xenon (Xe) with ethane (C 2 H 6 ) for pressures ranging from 6 to 10 Torr (8–10.6 mbar) and for low reduced electric fields in the 10 Td to 25 Td range (2.4–6.1 kV⋅cm −1 ⋅ bar −1 ), at room temperature. The time of arrival spectra revealed two peaks throughout the entire range studied which were attributed to ion species with 3-carbons (C 3 H 5 + , C 3 H 6 + C 3 H 8 + and C 3 H 9 + ) and with 4-carbons (C 4 H 7 + , C 4 H 9 + and C 4 H 10 + ). Besides these, and for Xe concentrations above 70%, a bump starts to appear at the right side of the main peak for reduced electric fields higher than 20 Td, which was attributed to the resonant charge transfer of C 2 H 6 + to C 2 H 6 that affects the mobility of its ion products (C 3 H 8 + and C 3 H 9 + ). The time of arrival spectra for Xe concentrations of 20%, 50%, 70% and 90% are presented, together with the reduced mobilities as a function of the Xe concentration calculated from the peaks observed for the low reduced electric fields and pressures studied.

  5. MARVEL analysis of the rotational-vibrational states of the molecular ions H2D+ and D2H+.

    Science.gov (United States)

    Furtenbacher, Tibor; Szidarovszky, Tamás; Fábri, Csaba; Császár, Attila G

    2013-07-07

    Critically evaluated rotational-vibrational line positions and energy levels, with associated critically reviewed labels and uncertainties, are reported for two deuterated isotopologues of the H3(+) molecular ion: H2D(+) and D2H(+). The procedure MARVEL, standing for Measured Active Rotational-Vibrational Energy Levels, is used to determine the validated levels and lines and their self-consistent uncertainties based on the experimentally available information. The spectral ranges covered for the isotopologues H2D(+) and D2H(+) are 5.2-7105.5 and 23.0-6581.1 cm(-1), respectively. The MARVEL energy levels of the ortho and para forms of the ions are checked against ones determined from accurate variational nuclear motion computations employing the best available adiabatic ab initio potential energy surfaces of these isotopologues. The number of critically evaluated, validated and recommended experimental (levels, lines) are (109, 185) and (104, 136) for H2D(+) and D2H(+), respectively. The lists of assigned MARVEL lines and levels and variational levels obtained for H2D(+) and D2H(+) as part of this study are deposited in the ESI to this paper.

  6. The H+ ECR source for the LAMPF Optically Pumped Polarized Ion Source

    International Nuclear Information System (INIS)

    York, R.L.; Tupa, D.

    1990-01-01

    An ECR source is used to produce the H + beam for the Optically Pumped Polarized Ion Source (OPPIS) at LAMPF. OPPIS requires a very high H + beam brightness from the ECR source. Studies of ECR extraction geometries that best fulfill this requirement are presented. 8 refs., 4 figs., 1 tab

  7. Comments on H- volume production in Cs-seeded ion sources. Appendix I

    International Nuclear Information System (INIS)

    Peterson, J.R.

    1986-01-01

    Considerable interest was generated at the IAEA Negative Ion Beam Workshop in Grenoble, France, in March, 1985, by a report from the Kurchatov Institute on the development of a 2-ampere steady-state H - ion source, in which the ions were volume-produced in a discharge in H 2 , seeded with Cs vapor. The mechanism primarily responsible for this remarkably high current from a volume production source was not yet understood, but it was tentatively presumed to involve the collisional energy transfer from electronically excited Cs 6p atoms into H 2 vibrations. In any case, it was apparently different from the surface-plasma interactions that have been assumed to control the H - production in the Dudnikov-Dimov type sources

  8. Extraction of volume produced H- or D- ions from a sheet plasma, 2

    International Nuclear Information System (INIS)

    Uramoto, Joshin.

    1984-02-01

    A development to large area H - or D - ion source is tried by using three extraction electrodes: The first electrode bias voltage is set near the wall potential (floating), the second electrode is set near 13 % of main extraction voltage and the third electrode is the main acceleration electrode. An ion current of 13 mA (3.3 mA/cm 2 ) for H - or 11 mA (2.8 mA/ cm 2 ) for D - at 3 KeV is extracted from 9 apertures of 6 mm phi in 4 cm 2 outside of the sheet plasma (14 cm wide and 1.0 cm thick) under a pressure of 7.7 x 10 -4 H2 or D2 gas and a weak magnetic field 50 gauss. Then, it is noted that the corresponding electron current is suppressed below 1/10 of the H - or D - ion current. (author)

  9. Observation of high-lying resonances in the H- ion

    International Nuclear Information System (INIS)

    Harris, P.G.; New Mexico Univ., Albuquerque, NM

    1990-05-01

    This dissertation reports the observation of several series of resonances, for which both electrons are in excited states, in the photodetachment cross section of H - . These 1 P doubly-excited states interfere with the continuum in which they are embedded, and appear as dips in the production cross section of excited neutral hydrogen. The experiment was performed by intersecting an 800 MeV H - beam with a (266 nm) laser beam at varying angles; the relativistic Doppler shift then ''tuned'' the photon energy in the barycentric frame. The process was observed by using a magnet strong enough the strip the electrons from the excited hydrogen atoms in selected states n and detecting the resulting protons, which allowed the isolation of the individual n channels. Three resonances are clearly visible in each channel. The data support recent theoretical calculations for the positions of doubly-excited 1 P resonances, and verify a new Rydberg-like formula for the modified Coulomb potential

  10. Deep level defects in 4H-SiC introduced by ion implantation: the role of single ion regime.

    Science.gov (United States)

    Pastuović, Željko; Siegele, Rainer; Capan, Ivana; Brodar, Tomislav; Sato, Shin-Ichiro; Ohshima, Takeshi

    2017-11-29

    We characterized intrinsic deep level defects created in ion collision cascades which were produced by patterned implantation of single accelerated 2.0 MeV He and 600 keV H ions into n-type 4H-SiC epitaxial layers using a fast-scanning reduced-rate ion microbeam. The initial deep level transient spectroscopy measurement performed on as-grown material in the temperature range 150-700 K revealed the presence of only two electron traps, Z 1/2 (0.64 eV) and EH 6/7 (1.84 eV) assigned to the two different charge state transitions of the isolated carbon vacancy, V C (=/0) and (0/+). C-V measurements of as-implanted samples revealed the increasing free carrier removal with larger ion fluence values, in particular at depth corresponding to a vicinity of the end of an ion range. The first DLTS measurement of as-implanted samples revealed formation of additional deep level defects labelled as ET1 (0.35 eV), ET2 (0.65 eV) and EH3 (1.06 eV) which were clearly distinguished from the presence of isolated carbon vacancies (Z 1/2 and EH 6/7 defects) in increased concentrations after implantations either by He or H ions. Repeated C-V measurements showed that a partial net free-carrier recovery occurred in as-implanted samples upon the low-temperature annealing following the first DLTS measurement. The second DLTS measurement revealed the almost complete removal of ET2 defect and the partial removal of EH3 defect, while the concentrations of Z 1/2 and EH 6/7 defects increased, due to the low temperature annealing up to 700 K accomplished during the first temperature scan. We concluded that the ET2 and EH3 defects: (i) act as majority carrier removal traps, (ii) exhibit a low thermal stability and (iii) can be related to the simple point-like defects introduced by light ion implantation, namely interstitials and/or complex of interstitials and vacancies in both carbon and silicon sub-lattices.

  11. Determination of the maximum retention of cobalt by ion exchange in h-zeolites

    Directory of Open Access Journals (Sweden)

    A. S. Zola

    2012-06-01

    Full Text Available This work aimed to determine the maximum content of cobalt that can be incorporated by ion exchange in zeolites H-USY, H-Beta, H-Mordenite, and H-ZSM-5. To reach this goal, batch isotherms at 75ºC were constructed after addition of zeolite samples in flasks filled with cobalt nitrate solution. The equilibrium data were fitted to Langmuir, Freundlich, and Tóth adsorption isotherm models. Langmuir was the best model for zeolites H-Beta, H-Mordenite, and H-ZSM-5, whereas experimental data for H-USY were better fitted to the Freundlich isotherm model. From the isotherms, it was possible to determine the maximum cobalt exchange level (q max that can be incorporated in each zeolite through ion exchange. In this sense, H-USY presented the highest q max value (2.40 meq/g zeol, while H-ZSM-5 showed the lowest one (0.64 meq/g zeol. These results also show the influence of the zeolite framework related to the channel system, pore opening, presence of cavities and secondary porosity and SiO2/Al2O3 ratio (SAR on the maximum capacity and behavior of cobalt ion exchange in protonic zeolites.

  12. Status of the SNS H- ion source and low-energy beam transport system

    International Nuclear Information System (INIS)

    Keller, R.; Thomae, R.; Stockli, M.; Welton, R.

    2002-01-01

    The ion source and Low-Energy Transport (LEBT) system that will provide H - ion beams to the Spallation Neutron Source (SNS) Front End and the accelerator chain have been developed into a mature unit that will satisfy the operational needs through the commissioning and early operating phases of SNS. The ion source was derived from the SSC ion source, and many of its original features have been improved to achieve reliable operation at 6% duty factor, producing beam currents in the 35-mA range and above. The LEBT utilizes purely electrostatic focusing and includes static beam-steering elements and a pre-chopper. This paper will discuss the latest design features of the ion source and LEBT, give performance data for the integrated system, and report on relevant commissioning results obtained with the SNS RFQ accelerator. Perspectives for further improvements will be outlined in concluding remarks

  13. Ion beam analysis of a-C:H films on alloy steel substrate

    International Nuclear Information System (INIS)

    Silva, T.F.; Moro, M.V.; Trindade, G.F.; Added, N.; Tabacniks, M.H.; Santos, R.J.; Santana, P.L.; Bortoleto, J.R.R.

    2013-01-01

    An a-C:H thin film deposited by plasma immersion ion implantation and deposition on alloy steel (16MnCr5) was analyzed using a self-consistent ion beam analysis technique. In the self-consistent analysis, the results of each individual technique are combined in a unique model, increasing confidence and reducing simulation errors. Self-consistent analysis, then, is able to improve the regular ion beam analysis since several analyses commonly used to process ion beam data still rely on handling each spectrum independently. The sample was analyzed by particle-induced x-ray emission (for trace elements), elastic backscattering spectrometry (for carbon), forward recoil spectrometry (for hydrogen) and Rutherford backscattering spectrometry (for film morphology). The self-consistent analysis provided reliable chemical information about the film, despite its “heavy” substrate. As a result, we could determine precisely the H/C ratio, contaminant concentration and some morphological characteristics of the film, such as roughness and discontinuities. - Highlights: • Self-consistent approach of ion beam analysis was used to characterize an a-C:H film. • The self-consistent analysis provided a unequivocal and reliable model of the sample. • Morphological aspects of the film were assessed with the ion beam analysis

  14. Chemical sputtering by H{sub 2}{sup +} and H{sub 3}{sup +} ions during silicon deposition

    Energy Technology Data Exchange (ETDEWEB)

    Landheer, K., E-mail: c.landheer@uu.nl; Poulios, I.; Rath, J. K. [Debye Institute for Nanomaterials Science-Physics of Devices, Utrecht University, 5656 AE Eindhoven (Netherlands); Goedheer, W. J. [FOM Institute DIFFER-Dutch Institute for Fundamental Energy Research, 5600 HH Eindhoven (Netherlands); Schropp, R. E. I. [Department of Applied Physics, Plasma and Materials Processing, Eindhoven University of Technology, 5600 MB Eindhoven (Netherlands)

    2016-08-07

    We investigated chemical sputtering of silicon films by H{sub y}{sup +} ions (with y being 2 and 3) in an asymmetric VHF Plasma Enhanced Chemical Vapor Deposition (PECVD) discharge in detail. In experiments with discharges created with pure H{sub 2} inlet flows, we observed that more Si was etched from the powered than from the grounded electrode, and this resulted in a net deposition on the grounded electrode. With experimental input data from a power density series of discharges with pure H{sub 2} inlet flows, we were able to model this process with a chemical sputtering mechanism. The obtained chemical sputtering yields were (0.3–0.4) ± 0.1 Si atom per bombarding H{sub y}{sup +} ion at the grounded electrode and at the powered electrode the yield ranged from (0.4 to 0.65) ± 0.1. Subsequently, we investigated the role of chemical sputtering during PECVD deposition with a series of silane fractions S{sub F} (S{sub F}(%) = [SiH{sub 4}]/[H{sub 2}]*100) ranging from S{sub F} = 0% to 20%. We experimentally observed that the SiH{sub y}{sup +} flux is not proportional to S{sub F} but decreasing from S{sub F} = 3.4% to 20%. This counterintuitive SiH{sub y}{sup +} flux trend was partly explained by an increasing chemical sputtering rate with decreasing S{sub F} and partly by the reaction between H{sub 3}{sup +} and SiH{sub 4} that forms SiH{sub 3}{sup +}.

  15. Cross sections and transport coefficients for H3+ H3+ png" mimetype="image" xlink:href="d170295-eq1.png"/> H3+ ions in water vapour★

    Science.gov (United States)

    Stojanović, Vladimir; Raspopović, Zoran; Jovanović, Jasmina; Nikitović, Željka; Marić, Dragana; Petrović, Zoran Lj.

    2017-11-01

    Scattering cross sections for positive H3+ ions in water vapour were calculated by a simple but quite general theory and then assessed by using the available data. Transport coefficients for H3+ ions in water vapour in DC fields were calculated by using a Monte Carlo simulation from low to moderate reduced electric fields E/N (E is electric field and N is gas number density) where the non-conservative collisions are also taken into account. Contribution to the Topical Issue "Physics of Ionized Gases (SPIG 2016)", edited by Goran Poparic, Bratislav Obradovic, Dragana Maric and Aleksandar Milosavljevic.

  16. An Approach towards a Long-life, Microwave-assisted H- Ion Soucre for Proton Drivers

    International Nuclear Information System (INIS)

    Keller, R.; Regis, M.; Wallig, J.; Hahto, S.; Monroy, M.; Ratti, A.; Syversrud, D.; Welton, R.; Anderson, D.

    2005-01-01

    This paper reports on experiments aimed at developing a new high-intensity H - ion source with long lifetime whose concept had recently been introduced. Starting from the motivation for this effort, several steps of the earlier development work are recapitulated, and the performance of the latest design variant is discussed in detail. The basic concept consists in coupling an ECR ion source to a standard SNS multi-cusp H - ion source that is driven by pulsed dc, rather than rf, power. As a key result, an electron beam of 1.5 A current has been extracted from the ECR discharge operating at 1.9 kW c. w. power, and a maximum discharge current of 17.5 A was achieved in the H - ion source. Production of H - ions, however could not yet been demonstrated in the one, preliminary, experiment conducted so far. The paper concludes by outlining further envisaged development steps for the plasma generator and an expansion towards a novel extraction system

  17. Photodissociation of H2+ by a ruby laser with ion energy analysis of ejected H+

    International Nuclear Information System (INIS)

    Ozenne, J.B.; Pham, D.; Tadjeddine, M.; Durup, J.

    1974-01-01

    The kinetic energy released in the photodissociation of H 2 + by a ruby laser beam has been measured. The spectrum of the dissociation kinetic energy of H + +H shows several vibrational levels, and after deconvolution due to the energetic and angular resolution of the apparatus, gives a population of those vibrational levels, close to theoretical population [fr

  18. Large source test stand for H-(D-) ion source

    International Nuclear Information System (INIS)

    Larson, R.; McKenzie-Wilson, R.

    1981-01-01

    The Brookhaven National Laboratory Neutral Beam Group has constructed a large source test stand for testing of the various source modules under development. The first objective of the BNL program is to develop a source module capable of delivering 10A of H - (D - ) at 25 kV operating in the steady state mode with satisfactory gas and power efficiency. The large source test stand contains gas supply and vacuum pumping systems, source cooling systems, magnet power supplies and magnet cooling systems, two arc power supplies rated at 25 kW and 50 kW, a large battery driven power supply and an extractor electrode power supply. Figure 1 is a front view of the vacuum vessel showing the control racks with the 36'' vacuum valves and refrigerated baffles mounted behind. Figure 2 shows the rear view of the vessel with a BNL Mk V magnetron source mounted in the source aperture and also shows the cooled magnet coils. Currently two types of sources are under test: a large magnetron source and a hollow cathode discharge source

  19. Reactions of HBr+ ions in the 2Π i , v + quantum states with H2 and HBr molecules

    Science.gov (United States)

    Belikov, A. E.; Smith, M. A.

    2008-05-01

    The mechanisms and kinetics of low-temperature ion-molecular reactions between the Br+, HBr+, and DBr+ions and the HBr, DBr, H2, and D2 molecules were studied. The HBr+ ( i, v +) and DBr+( i, v +) ions were prepared in separate spin-orbit ( i) and vibrational ( v +) states by resonance multiphoton ionization in a free flow of halogen halides (HBr and/or DBr) with hydrogen, deuterium, or inert gases (Ar, He). The effectiveness of various reaction channels, including the exchange of charges, H and D atoms, and H+andD+ ions, was studied. The quantitative data on the kinetics of these reactions were obtained for separate quantum states of the ions. The resonance ionization of one of the two ion isotopomers H79Br+(D79Br+) or H81Br+(D81Br+) was used to study and compare the effectiveness of various ion-molecular reaction channels.

  20. Recombination of H+3 ions in the afterglow of a He-Ar-H2 plasma

    International Nuclear Information System (INIS)

    Glosik, J; Korolov, I; Plasil, R; Novotny, O; Kotrik, T; Hlavenka, P; Varju, J; Mikhailov, I A; Kokoouline, V; Greene, Chris H

    2008-01-01

    Recombination of H + 3 with electrons is studied in a low-temperature plasma containing He, H 2 and Ar at different He and H 2 densities. The effective plasma recombination rate is driven by binary, H + 3 + e - , and ternary, H + 3 + e - + He, processes with the rate coefficients 7.5 x 10 -8 cm 3 s -1 and 2.8 x 10 -25 cm 6 s -1 respectively at 260 K. We suggest that the ternary recombination involves formation of neutral highly excited Rydberg H 3 followed by an l-changing collision with He. The difference between recombination of para- and ortho-H + 3 is discussed. (fast track communication)

  1. Transition metal swift heavy ion implantation on 4H-SiC

    Energy Technology Data Exchange (ETDEWEB)

    Ali, A. Ashraf; Kumar, J. [Crystal Growth Centre, Anna University, Chennai 600 025 (India); Ramakrishnan, V. [Indian Institute of Science Education and Research, Thiruvanthapuram (India); Asokan, K. [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110 067 (India)

    2016-03-01

    This work reports on the realization of Quantum Ring (QR) and Quantum Dot (QD) like structures on 4H-SiC through SHI implantation and on their Raman studies. 4H-SiC is SHI implanted with Transition Metal (TM) Ni ion at different fluences. It is observed that a vibrational mode emerges as the result of Ni ion implantation. The E{sub 2} (TO) and the A{sub 1} (LO) are suppressed as the fluence increases. In this paper Raman and AFM studies have been performed at room temperature and the queer anomalies are addressed so new devices can be fabricated.

  2. Transition metal swift heavy ion implantation on 4H-SiC

    Science.gov (United States)

    Ali, A. Ashraf; Kumar, J.; Ramakrishnan, V.; Asokan, K.

    2016-03-01

    This work reports on the realization of Quantum Ring (QR) and Quantum Dot (QD) like structures on 4H-SiC through SHI implantation and on their Raman studies. 4H-SiC is SHI implanted with Transition Metal (TM) Ni ion at different fluences. It is observed that a vibrational mode emerges as the result of Ni ion implantation. The E2 (TO) and the A1 (LO) are suppressed as the fluence increases. In this paper Raman and AFM studies have been performed at room temperature and the queer anomalies are addressed so new devices can be fabricated.

  3. Ion-ion correlation, solvent excluded volume and pH effects on physicochemical properties of spherical oxide nanoparticles.

    Science.gov (United States)

    Ovanesyan, Zaven; Aljzmi, Amal; Almusaynid, Manal; Khan, Asrar; Valderrama, Esteban; Nash, Kelly L; Marucho, Marcelo

    2016-01-15

    One major source of complexity in the implementation of nanoparticles in aqueous electrolytes arises from the strong influence that biological environments has on their physicochemical properties. A key parameter for understanding the molecular mechanisms governing the physicochemical properties of nanoparticles is the formation of the surface charge density. In this article, we present an efficient and accurate approach that combines a recently introduced classical solvation density functional theory for spherical electrical double layers with a surface complexation model to account for ion-ion correlation and excluded volume effects on the surface titration of spherical nanoparticles. We apply the proposed computational approach to account for the charge-regulated mechanisms on the surface chemistry of spherical silica (SiO2) nanoparticles. We analyze the effects of the nanoparticle size, as well as pH level and electrolyte concentration of the aqueous solution on the nanoparticle's surface charge density and Zeta potential. We validate our predictions for 580Å and 200Å nanoparticles immersed in acid, neutral and alkaline mono-valent aqueous electrolyte solutions against experimental data. Our results on mono-valent electrolyte show that the excluded volume and ion-ion correlations contribute significantly to the surface charge density and Zeta potential of the nanoparticle at high electrolyte concentration and pH levels, where the solvent crowding effects and electrostatic screening have shown a profound influence on the protonation/deprotonation reactions at the liquid/solute interface. The success of this approach in describing physicochemical properties of silica nanoparticles supports its broader application to study other spherical metal oxide nanoparticles. Copyright © 2015 Elsevier Inc. All rights reserved.

  4. Radiation effects induced in H2O ice by high energy ions and astrophysical applications

    International Nuclear Information System (INIS)

    Benit, J.

    1987-06-01

    This thesis presents the study of radiation effects induced in H 2 O ice by MeV/u ions: desorption of ionized species, erosion of the irradiated film and molecular synthesis within the ice. The desorption is analysed by time of flight mass spectroscopy. We describe the mass spectra of the desorbed ions, both positively and negatively charged, up to 400 uma. The absolute yields are given, as well as their dependence with the energy and energy loss of the primary ions. The erosion of the ice is analyzed by infrared spectroscopy, on line during the irradiation. Absolute yields are derived, as a function of the ions beam flux, the mass and energy of the ions, and the thickness of the samples. A linear dependence of the yield with the thickness is interpreted as follows: the erosion comes primarily from the dissociation of the molecules all along the ion tracks. Some astrophysical implications of the results are discussed in the framework of irradiation of icy material in a variety of environments: magnetospheres of giant planets, cometary nuclei, circumstellar shells and molecular clouds. It is emphasized that the irradiation by energetic ions plays a major role in cosmochemistry [fr

  5. Energy transfer between energetic ring current H(+) and O(+) by electromagnetic ion cyclotron waves

    Science.gov (United States)

    Thorne, Richard M.; Horne, Richard B.

    1994-01-01

    Electromagnetic ion cyclotron (EMIC) waves in the frequency range below the helium gyrofrequency can be excited in the equatorial region of the outer magnetosphere by cyclotron resonant instability with anisotropic ring current H(+) ions. As the unducted waves propagate to higher latitudes, the wave normal should become highly inclined to the ambient magnetic field. Under such conditions, wave energy can be absorbed by cyclotron resonant interactions with ambient O(+), leading to ion heating perpendicular to the ambient magnetic field. Resonant wave absorption peaks in the vicinity of the bi-ion frequency and the second harmonic of the O(+) gyrofrequrency. This absorption should mainly occur at latitudes between 10 deg and 30 deg along auroral field lines (L is greater than or equal to 7) in the postnoon sector. The concomitant ion heating perpendicular to the ambient magnetic field can contribute to the isotropization and geomagnetic trapping of collapsed O(+) ion conics (or beams) that originate from a low-altitude ionospheric source region. During geomagnetic storms when the O(+) content of the magnetosphere is significantly enhanced, the absorption of EMIC waves should become more efficient, and it may contribute to the observed acceleration of O(+) ions of ionospheric origin up to ring current energies.

  6. Ettringite and C-S-H Portland cement phases for waste ion immobilization: A review

    International Nuclear Information System (INIS)

    Gougar, M.L.D.; Scheetz, B.E.; Roy, D.M.

    1996-01-01

    The formation, structure and chemistry of the ettringite and C-S-H phases of Portland cement have been reviewed as they relate to waste ion immobilization. The purpose of this review was to investigate the use of Portland cement as a host for priority metallic pollutants as identified by the Environmental Protection Agency and as a host for radioactive waste ions as identified in 40 CFR 191. Ettringite acts as host to a number of these ions in both the columnar and channel sections of the crystal structure. Substitutions have been made at the calcium, aluminum, hydroxide and sulfate sites. C-S-H also hosts a number of the waste species in both ionic and salt form. Immobilization mechanisms for C-S-H include sorption, phase mixing and substitution. The following ions have not apparently been reported as specifically immobilized by one of these phases: Ag, Am, Np, Pu, Ra, Tc, Th and Sn; however, some of these ions are immobilized by Portland cement

  7. Recombination of KrD{sup +} and KrH{sup +} ions in afterglow plasma

    Energy Technology Data Exchange (ETDEWEB)

    Korolov, I; Kotrik, T; Plasil, R; Hejduk, M; Varju, J; Dohnal, P; Glosik, J, E-mail: juraj.glosik@mff.cuni.c [Department of Surface and Plasma Science, Faculty of Mathematics and Physics, Charles University in Prague (Czech Republic)

    2009-11-15

    Reported is flowing afterglow (FALP) study of recombination of KrH{sup +} and KrD{sup +} ions with electrons at 250 K in mixtures of He/Kr/H{sub 2} and He/Kr/D{sub 2}, respectively. The influence of fast recombining cluster ions formation on apparent effective recombination rate coefficients ({alpha}{sub eff}) was measured and used in data analysis. The obtained binary rate coefficients for recombination of KrH{sup +} and KrD{sup +} are {alpha}{sub KrH+} = 2x10{sup -8} cm{sup 3}s{sup -1} and {alpha}{sub KrD+} = 1x10{sup -8} cm{sup 3}s{sup -1}.

  8. H2+ molecular ion in a strong magnetic field: Ground state

    International Nuclear Information System (INIS)

    Turbiner, A. V.; Lopez Vieyra, J. C.

    2003-01-01

    A detailed quantitative analysis of the system of two protons and one electron (ppe) placed in magnetic field ranging from 10 9 -4.414x10 13 G is presented. The present study is focused on the question of the existence of the molecular ion H 2 + in a magnetic field. A variational method with an optimization of the form of the vector potential (optimal gauge fixing) is used as a tool. It is shown that in the domain of applicability of the nonrelativistic approximation the (ppe) system in the Born-Oppenheimer approximation has a well-pronounced minimum in the total energy at a finite interproton distance for B(less-or-similar sign)10 11 G, thus manifesting the existence of H 2 + . For B(greater-or-similar sign)10 11 G and large inclinations (of the molecular axis with respect to the magnetic line) the minimum disappears and hence the molecular ion H 2 + does not exist. It is shown that the most stable configuration of H 2 + always corresponds to protons situated along the magnetic line. With magnetic field growth the H 2 + ion becomes more and more tightly bound and compact, and the electronic distribution evolves from a two-peak to a one-peak pattern. The domain of inclinations where the H 2 + ion exists reduces with magnetic field increase and finally becomes 0 degree sign -25 degree sign at B=4.414x10 13 G. Phase-transition-type behavior of variational parameters for some interproton distances related to the beginning of the chemical reaction H 2 + ↔H+p is found

  9. Blistering in alloy Ti–6Al–4V from H + ion implantation

    Indian Academy of Sciences (India)

    6Al–4V, was studied, following H+ ion implantation of 150 keV and 250 keV energy to fluence of 2.6 × 1018 cm-2 and 2.5 × 1019 cm-2, respectively at ambient temperature. No detectable change was observed in surface features of either of the ...

  10. Power efficiency improvements with the radio frequency H{sup −} ion source

    Energy Technology Data Exchange (ETDEWEB)

    Kalvas, T., E-mail: taneli.kalvas@jyu.fi; Tarvainen, O.; Komppula, J.; Koivisto, H.; Tuunanen, J. [Department of Physics, University of Jyväskylä, P.O. Box 35 (YFL), FI-40014 Jyväskylä (Finland); Potkins, D.; Stewart, T.; Dehnel, M. [D-Pace, Inc., P.O. Box 201, Nelson, British Columbia V1L 5P9 (Canada)

    2016-02-15

    CW 13.56 MHz radio frequency-driven H{sup −} ion source is under development at the University of Jyväskylä for replacing an existing filament-driven ion source at the MCC30/15 cyclotron. Previously, production of 1 mA H{sup −} beam, which is the target intensity of the ion source, has been reported at 3 kW of RF power. The original ion source front plate with an adjustable electromagnet based filter field has been replaced with a new front plate with permanent magnet filter field. The new structure is more open and enables a higher flux of ro-vibrationally excited molecules towards the plasma electrode and provides a better control of the potential near the extraction due to a stronger separation of the main plasma from the plasma electrode. While the original system provided better control over the e{sup −}/H{sup −} ratio, the new configuration has led to a higher production efficiency of 1 mA H{sup −} at 1.75 kW RF power. The latest results and upgrade plans are presented.

  11. Blistering in alloy Ti–6Al–4V from H+ ion implantation

    Indian Academy of Sciences (India)

    Administrator

    technology owing to their high specific strength and cor- rosion resistance. Structural components in space tech- nology experience different types of radiations, therefore, their stability in such environments becomes an important consideration for their suitability. Stability of titanium and its alloys against H. + ion irradiation is ...

  12. The Cascaded Arc: High Flows of Rovibrationally Excited H2 and its Impact on H- Ion Formation

    International Nuclear Information System (INIS)

    Gabriel, O.; Harskamp, W. E. N. van; Schram, D. C.; Sanden, M. C. M. van de; Engeln, R.

    2009-01-01

    The cascaded arc is a plasma source providing high fluxes of excited and reactive species such as ions, radicals and rovibrationally excited molecules. The plasma is produced under pressures of some kPa in a direct current arc with electrical powers up to 10 kW. The plasma leaves the arc channel through a nozzle and expands with supersonic velocity into a vacuum-chamber kept by pumps at low pressures. We investigated the case of a pure hydrogen plasma jet with and without an applied axial magnetic field that confines ions and electrons in the jet. Highly excited molecules and atoms were detected by means of laser-induced fluorescence and optical emission spectroscopy. In case of an applied magnetic field the atomic state distribution of hydrogen atoms shows an overpopulation between the electronic states p = 5, 4 and 3. The influence of the highly excited hydrogen molecules on H - ion formation and a possible mechanism involving this negative ion and producing atomic hydrogen in state p = 3 will be discussed.

  13. Nuclear Spin Effect on Recombination of H3+ Ions with Electrons at 77 K

    Science.gov (United States)

    Varju, J.; Hejduk, M.; Dohnal, P.; Jílek, M.; Kotrík, T.; Plašil, R.; Gerlich, D.; Glosík, J.

    2011-05-01

    Utilizing different ratios of para to ortho H2 in normal and para enriched hydrogen, we varied the population of para-H3+ in an H3+ dominated plasma at 77 K. Absorption spectroscopy was used to measure the densities of the two lowest rotational states of H3+. Monitoring plasma decays at different populations of para-H3+ allowed us to determine the rate coefficients for binary recombination of H3+ and ortho-H3+ ions: αbinp(77K)=(1.9±0.4)×10-7cm3s-1 and αbino(77K)=(0.2±0.2)×10-7cm3s-1.

  14. Nuclear Spin Effect on Recombination of H3+ Ions with Electrons at 77 K

    International Nuclear Information System (INIS)

    Varju, J.; Hejduk, M.; Dohnal, P.; Jilek, M.; Kotrik, T.; Plasil, R.; Gerlich, D.; Glosik, J.

    2011-01-01

    Utilizing different ratios of para to ortho H 2 in normal and para enriched hydrogen, we varied the population of para-H 3 + in an H 3 + dominated plasma at 77 K. Absorption spectroscopy was used to measure the densities of the two lowest rotational states of H 3 + . Monitoring plasma decays at different populations of para-H 3 + allowed us to determine the rate coefficients for binary recombination of H 3 + and ortho-H 3 + ions: p α bin (77 K)=(1.9±0.4)x10 -7 cm 3 s -1 and o α bin (77 K)=(0.2±0.2)x 10 -7 cm 3 s -1 .

  15. Systematic generation of buffer systems for pH gradient ion exchange chromatography and their application.

    Science.gov (United States)

    Kröner, Frieder; Hubbuch, Jürgen

    2013-04-12

    pH gradient protein separations are widely used techniques in the field of protein analytics, of which isoelectric focusing is the most well known application. The chromatographic variant, based on the formation of pH gradients in ion exchange columns is only rarely applied due to the difficulties to form controllable, linear pH gradients over a broad pH range. This work describes a method for the systematic generation of buffer compositions with linear titration curves, resulting in well controllable pH gradients. To generate buffer compositions with linear titration curves an in silico method was successfully developed. With this tool, buffer compositions for pH gradient ion exchange chromatography with pH ranges spanning up to 7.5 pH units were established and successfully validated. Subsequently, the buffer systems were used to characterize the elution behavior of 22 different model proteins in cation and anion exchange pH gradient chromatography. The results of both chromatographic modes as well as isoelectric focusing were compared to describe differences in between the methods. Copyright © 2013 Elsevier B.V. All rights reserved.

  16. Hydrogen constituents of the mesosphere inferred from positive ions - H2O, CH4, H2CO, H2O2, and HCN

    Science.gov (United States)

    Kopp, E.

    1990-01-01

    The concentrations in the mesosphere of H2O, CH4, H2CO, H2O2, and HCN were inferred from data on positive ion compositions, obtained from one mid-latitude and four high-latitude rocket flights. The inferred concentrations were found to agree only partially with the ground-based microwave measurements and/or model prediction by Garcia and Solomon (1985). The CH4 concentration was found to vary between 70 and 4 ppb in daytime and 900 and 100 ppbv at night, respectively. Unexpectedly high H2CO concentrations were obtained, with H2CO/H2O ratios between 0.0006 and 0.1, and a mean HCN volume mixing ratio of 6 x 10 to the -10th was inferred.

  17. Investigations of steel 1H18N9T surface roughness exposed to ion beam from glow ion source with cavity anode; Badanie chropowatosci powierzchni stali 1H18N9T bombardowanej wiazka z jarzeniowego zrodla z wnekowa anoda

    Energy Technology Data Exchange (ETDEWEB)

    Wilk, J.; Kowalski, Z.W. [Politechnika Wroclawska, Wroclaw (Poland)

    1997-12-01

    The stainless steel (1H18N9T) surface properties have been investigated in the course of ion beam exposition. The influence of glancing angle (in the range of 80-90 deg) and ion dose from glow ion source with cavity anode on steel roughness has been presented. It has been concluded the applicability of used type of ion beam source for steel surface treatment. 8 refs, 1 fig.

  18. High energy ion irradiation effects in H2O ice and astrophysical applications

    International Nuclear Information System (INIS)

    Benit, J.

    1987-06-01

    This thesis presents the study of radiation effects induced in H 2 O ice by MeV/u ions: desorption of ionized species, ''erosion'' of the irradiated film and molecular synthesis within the ice. The desorption is analysed by time of flight mass spectroscopy. We describe the mass spectra of the desorbed ions, both positively and negatively charged, up to 400 uma. The absolute yields are given, as well as their dependence with the energy and energy loss of the primary ions. The ''erosion'' of the ice is analysed by infrared spectroscopy, on line during the irradiation. Absolute yields are derived, as a function of the ions beam flux, the mass and energy of the ions, and the thickness of the samples. A linear dependence of the yield with the thickness is interpreted as follows: the erosion comes primarely from the dissociation of the molecules all along the ion tracks. In conclusion some astrophysical implications of the results are discussed in the framework of irradiation of icy material in a variety of environments [fr

  19. Reactions of N+ (3P) ions with H2 and HD molecules at low temperatures

    Science.gov (United States)

    Grozdanov, Tasko P.; McCarroll, Ronald; Roueff, Evelyne

    2016-05-01

    Context. This work is motivated by the necessity to take account of both the nuclear spin symmetries of H2 and the spin-orbit interaction of N+ ions in order to investigate gas phase reactions in interstellar chemistry, leading to the formation of nitrogenous and deuterated compounds. Aims: The main objective in this work is to determine the rate coefficients for each possible initial quantum state of the reactants N+ (3Pj) + H2 (J) (and their isotopic variants). Only in this way does it become possible both to analyse experimental data and to develop realistic applications to interstellar chemical models to constrain the gas phase chemistry of ammonia and its isotopologues. Methods: A statistical treatment is presented of state selective reactive collisions involving N+ ions in fine structure state j with H2 or HD molecules in a rotation level J of the ground vibration state, leading either to the production of NH+ ions and H in the case of the H2 reactant, and to the production of either NH+ ions or ND+ in the case of the HD reactant. The energies of fine structure states (j = 0,1,2) of the N+ ions are treated on an equal footing with the other energies of internal motions. All fine structure states are considered to be reactive. Results: Cross sections for state-to-state collisions are calculated for collision energies ranging from 0.1-30 meV. These cross sections are then averaged over the kinetic energies of the reactants for each (J,j) to obtain the rate coefficients for a range of kinetic temperatures 10-200 K. The exo/endothermicity of the reactions involving N+ (3Pj) + H2 (J) (and isotopic variants) is derived from the difference ΔEe between the dissociation energies of the electronic molecular potentials of NH+ and H2. The value ΔEe = 101 meV is found to satisfactorily reproduce the experiments performed with ortho-H2 and to a lesser extent with para-H2. This value is used to determine the rate coefficient of the N+ + HD reaction leading to the

  20. Ultra-shallow junction formation by B18H22 ion implantation

    International Nuclear Information System (INIS)

    Kawasaki, Y.; Kuroi, T.; Yamashita, T.; Horita, K.; Hayashi, T.; Ishibashi, M.; Togawa, M.; Ohno, Y.; Yoneda, M.; Horsky, Tom; Jacobson, Dale; Krull, Wade

    2005-01-01

    We have investigated boron cluster implantation for ultra-shallow junction formation in transistors with gate lengths of ∼60nm. The use of large boron containing clusters is more advantageous than B + or BF 2 + implantation from the viewpoint of throughput and energy contamination. Ion implantation of B 18 H X + cluster ions, produced by ionizing B 18 H 22 (octadecaborane) vapor, was employed to fabricate the p-type SDE (source/drain extensions) of pMOSFETs. B 18 H X + implants with the energy and dose adjusted to produce equivalent projected range and B concentration as compared to conventional B + implants were carried out using a traditional implanter retrofitted with a SemEquip ClusterIon ( R) Source. The results on blank wafers and transistor performance on test pattern wafers were compared to standard monomer B + implants. Analysis of the blank wafers indicated that B 18 H X + showed the same or better characteristics than B + in junction depth and sheet resistance. Post-processing electrical measurements of the pMOSFETs implanted with B 18 H X + showed that they performed with nearly identical characteristics as ones implanted with B +

  1. Evaluation of pH and calcium ion release of calcium hydroxide pastes containing different substances.

    Science.gov (United States)

    Duarte, Marco Antônio Húngaro; Midena, Raquel Zanin; Zeferino, Márcia A; Vivan, Rodrigo Ricci; Weckwerth, Paulo Henrique; Dos Santos, Fernando; Guerreiro-Tanomaru, Juliane Maria; Tanomaru-Filho, Mário

    2009-09-01

    The objective of this study was to evaluate the pH and calcium ion release of calcium hydroxide pastes associated with different substances. Forty acrylic teeth with simulated root canals were divided into 4 groups according to the substance associated to the calcium hydroxide paste: chlorhexidine (CHX) in 2 formulations (1% solution and 2% gel), Casearia sylvestris Sw extract, and propylene glycol (control). The teeth with pastes and sealed coronal accesses were immersed in 10 mL deionized water. After 10 minutes, 24 hours, 48 hours, and 7, 15, and 30 days, the teeth were removed to another container, and the liquid was analyzed. Calcium ion release was measured by atomic absorption spectrophotometry, and pH readings were made with a pH meter. Data were analyzed statistically by analysis of variance and Tukey test (alpha = 0.05). Calcium analysis revealed significant differences (P .05) were observed among groups in the other periods. Regarding the pH, there were significant differences (P .05) were observed among groups. All pastes behaved similarly in terms of pH and calcium ion release in the studied periods.

  2. On the production of the positive antihydrogen ion {{\\bar{H}}^{+}} via radiative attachment

    Science.gov (United States)

    Keating, C. M.; Charlton, M.; Straton, Jack C.

    2014-11-01

    We provide an estimate of the cross section for the radiative attachment of a second positron into the (1{{S}2}{{ }1}{{S}e}) state of the {{\\bar{H}}+} ion using Ohmura and Ohmura’s (1960 Phys. Rev. 118 154) effective range theory and the principle of detailed balance. The {{\\bar{H}}+} ion can potentially be created using interactions of positrons with trapped antihydrogen, and our analysis includes a discussion in which estimates of production rates are given. Motivations to produce {{\\bar{H}}+} include its potential use as an intermediary to cool antihydrogen to ultra-cold (sub-mK) temperatures for a variety of studies, including spectroscopy and probing the gravitational interaction of the anti-atom.

  3. On the production of the positive antihydrogen ion H-bar + via radiative attachment

    International Nuclear Information System (INIS)

    Keating, C M; Straton, Jack C; Charlton, M

    2014-01-01

    We provide an estimate of the cross section for the radiative attachment of a second positron into the (1S 2 1 S e ) state of the H-bar + ion using Ohmura and Ohmura’s (1960 Phys. Rev. 118 154) effective range theory and the principle of detailed balance. The H-bar + ion can potentially be created using interactions of positrons with trapped antihydrogen, and our analysis includes a discussion in which estimates of production rates are given. Motivations to produce H-bar + include its potential use as an intermediary to cool antihydrogen to ultra-cold (sub-mK) temperatures for a variety of studies, including spectroscopy and probing the gravitational interaction of the anti-atom. (paper)

  4. Measurements of Linac4 H$^{-}$ ion source beam with a magnetized Einzel lens electron dump

    CERN Document Server

    Midttun, O; Scrivens, R

    2014-01-01

    Linac4 is a part of the upgrade of CERN’s accelerator complex for increased luminosity in the LHC. A new system to extract the ion beam from the plasma generator has been designed and tested, in order to improve the reliability and beam optics of the pulsed H- ion source. This paper presents the successfully implemented extraction system and three different beam measurements. The simulations compare well to the measurements and show that the plasma density was too low for the extraction system design during the measurements.

  5. Mathematical Modeling of Ni/H2 and Li-Ion Batteries

    Science.gov (United States)

    Weidner, John W.; White, Ralph E.; Dougal, Roger A.

    2001-01-01

    The modelling effort outlined in this viewgraph presentation encompasses the following topics: 1) Electrochemical Deposition of Nickel Hydroxide; 2) Deposition rates of thin films; 3) Impregnation of porous electrodes; 4) Experimental Characterization of Nickel Hydroxide; 5) Diffusion coefficients of protons; 6) Self-discharge rates (i.e., oxygen-evolution kinetics); 7) Hysteresis between charge and discharge; 8) Capacity loss on cycling; 9) Experimental Verification of the Ni/H2 Battery Model; 10) Mathematical Modeling Li-Ion Batteries; 11) Experimental Verification of the Li-Ion Battery Model; 11) Integrated Power System Models for Satellites; and 12) Experimental Verification of Integrated-Systems Model.

  6. H- Enhancement Process in a Multicusp Ion Source Operated with a Barium Insert Structure

    Energy Technology Data Exchange (ETDEWEB)

    Leung, K.N.; Van Os, C.F.A.; Kunkel, W.B.

    1990-05-01

    It has been demonstrated that the H{sup -} output current from a small multicusp source can be substantially enhanced if the hydrogen plasma is seeded with barium. Operating with a barium washer insert at the extraction aperture, it is found that the extractable H{sup -} current is increased by a factor of three if the insert bias potential is optimized. By use of a mixture of xenon and hydrogen gas, it is further demonstrated that the positive hydrogen ions are responsible for the observed H{sup -} enhancement.

  7. Rapid change of ion energy distribution and floating potential at L/H transition in the JFT-2M tokamak

    International Nuclear Information System (INIS)

    Miura, Y.; Nagashima, K.; Okano, F.

    1994-01-01

    Rapid changes of the main ion energy distribution at transitions from L-to-H, H-to-L and during ELMs are studied with the time of flight neutral measurement in the JFT-2M tokamak. The change of the main ion energy distribution after sawtooth crash during an L-mode phase is also studied. The change of the ion energy distribution just after sawtooth crash is the same as that at L/H-transition. The floating potential measured in the SOL also shows the rapid jump to more positive just after the sawtooth crash (at the same time of the change of an ion energy distribution). This shows the increase of ion outflux in the SOL and might correspond to the change of the ion energy distribution. This may be the reason why most of H-modes are triggered by a sawtooth. (author)

  8. pH buffers for sea water media based on the total hydrogen ion concentration scale

    Science.gov (United States)

    Dickson, Andrew G.

    1993-01-01

    Published e.m.f. values measured using the cell ? where p° = 101.325 kPa, and BH + and B are the conjugate acid-base pairs of 2-aminopyridine, 2-amino-2-hydroxymethyl-1,3-propanediol (tris), tetrahydro-1,4-isoxazine (morpholine), and 2-amino-2-methyl-1, 3-propanediol (bis), have been re-evaluated to assign pH values based on the "total" hydrogen ion concentration scale to equimolal ( m =0.04 mol kg -1) buffer solutions based on these compounds. These pH values are consistent with the best available equilibrium constants for acid-base processes in sea water and such pH buffers can be used as pH calibration standards to measure accurate values for oceanic pH on the "total" hydrogen ion pH scale. In addition, the published e.m.f. results for these various amine bases have been used to calculate their respective acidity constants on this pH scale.

  9. Studies on the Effect pH on the Sorption of Pb(II) and Cu(II) ions from ...

    African Journals Online (AJOL)

    The effect of pH on the sorption of Pb2+ and Cu2+ ion onto Nypa fruticans Wurmb biomass was investigated. Initial pH value of 2, 5, 7, 9, and 12 were used for this study with varying initial concentrations of metal ions. The experimental results were analyzed in terms of Langmuir, Freundlich and Flory-Huggins isotherms.

  10. Novel H+-Ion Sensor Based on a Gated Lateral BJT Pair

    Directory of Open Access Journals (Sweden)

    Heng Yuan

    2015-12-01

    Full Text Available An H+-ion sensor based on a gated lateral bipolar junction transistor (BJT pair that can operate without the classical reference electrode is proposed. The device is a special type of ion-sensitive field-effect transistor (ISFET. Classical ISFETs have the advantage of miniaturization, but  they are difficult to fabricate by a single fabrication process because of the bulky and brittle reference electrode materials. Moreover, the reference electrodes need to be separated from the sensor device in some cases. The proposed device is composed of two gated lateral BJT components, one of which had a silicide layer while the other was without the layer. The two components were operated under the metal-oxide semiconductor field-effect transistor (MOSFET-BJT hybrid mode, which can be controlled by emitter voltage and base current. Buffer solutions with different pH values were used as the sensing targets to verify the characteristics of the proposed device. Owing to their different sensitivities, both components could simultaneously detect the H+-ion concentration and function as a reference to each other. Per the experimental results, the sensitivity of the proposed device was found to be approximately 0.175 μA/pH. This experiment demonstrates enormous potential to lower the cost of the ISFET-based sensor technology.

  11. Novel H+-Ion Sensor Based on a Gated Lateral BJT Pair

    Science.gov (United States)

    Yuan, Heng; Zhang, Jixing; Cao, Chuangui; Zhang, Gangyuan; Zhang, Shaoda

    2015-01-01

    An H+-ion sensor based on a gated lateral bipolar junction transistor (BJT) pair that can operate without the classical reference electrode is proposed. The device is a special type of ion-sensitive field-effect transistor (ISFET). Classical ISFETs have the advantage of miniaturization, but  they are difficult to fabricate by a single fabrication process because of the bulky and brittle reference electrode materials. Moreover, the reference electrodes need to be separated from the sensor device in some cases. The proposed device is composed of two gated lateral BJT components, one of which had a silicide layer while the other was without the layer. The two components were operated under the metal-oxide semiconductor field-effect transistor (MOSFET)-BJT hybrid mode, which can be controlled by emitter voltage and base current. Buffer solutions with different pH values were used as the sensing targets to verify the characteristics of the proposed device. Owing to their different sensitivities, both components could simultaneously detect the H+-ion concentration and function as a reference to each other. Per the experimental results, the sensitivity of the proposed device was found to be approximately 0.175 μA/pH. This experiment demonstrates enormous potential to lower the cost of the ISFET-based sensor technology. PMID:26703625

  12. H32+ molecular ion in a strong magnetic field: Triangular configuration

    International Nuclear Information System (INIS)

    Lopez Vieyra, J.C.; Turbiner, A.V.

    2002-01-01

    The existence of the molecular ion H 3 2+ in a magnetic field in a triangular configuration is revised. A variational method with an optimization of the form of the vector potential (gauge fixing) is used. It is shown that in the range of magnetic fields 10 8 11 G the system (pppe), with the protons forming an equilateral triangle perpendicular to the magnetic line, has a well-pronounced minimum in the total energy. This configuration is unstable under the decays (H atom)+p+p and H 2 + +p. The triangular configuration of H 3 2+ complements H 3 2+ in the linear configuration that exists for B > or approx. 10 10 G

  13. RF H-minus ion source development in China spallation neutron source

    Science.gov (United States)

    Chen, W.; Ouyang, H.; Xiao, Y.; Liu, S.; Lü, Y.; Cao, X.; Huang, T.; Xue, K.

    2017-08-01

    China Spallation Neutron Source (CSNS) phase-I project currently uses a Penning surface plasma H- ion source, which has a life time of several weeks with occasional sparks between high voltage electrodes. To extend the life time of the ion source and prepare for the CSNS phase-II, we are trying to develop a RF negative hydrogen ion source with external antenna. The configuration of the source is similar to the DESY external antenna ion source and SNS ion source. However several changes are made to improve the stability and the life time. Firstly, Si3N4 ceramic with high thermal shock resistance, and high thermal conductivity is used for plasma chamber, which can endure an average power of 2000W. Secondly, the water-cooled antenna is brazed on the chamber to improve the energy efficiency. Thirdly, cesium is injected directly to the plasma chamber if necessary, to simplify the design of the converter and the extraction. Area of stainless steel exposed to plasma is minimized to reduce the sputtering and degassing. Instead Mo, Ta, and Pt coated materials are used to face the plasma, which makes the self-cleaning of the source possible.

  14. VUV emission spectroscopy combined with H- density measurements in the ion source Prometheus I

    Science.gov (United States)

    Aleiferis, S.; Laulainen, J.; Svarnas, P.; Tarvainen, O.; Bacal, M.; Béchu, S.

    2017-08-01

    "Prometheus I" is a volume H- negative ion source, driven by a network of dipolar electron cyclotron resonance (ECR; 2.45 GHz) modules. The vacuum-ultraviolet (VUV) emission spectrum of low-temperature hydrogen plasmas may be related to molecular and atomic processes involved directly or indirectly in the production of negative ions. In this work, VUV spectroscopy has been performed in the above source, Prometheus I, both in the ECR zones and the bulk (far from ECR zones and surfaces) plasma. The acquired VUV spectra are correlated with the negative ion densities, as measured by means of laser photodetachment, and the possible mechanisms of negative ion production are considered. The well-established H- formation process of dissociative attachment to vibrationally excited molecules is evaluated, while an additional production path (i.e. neutral resonant ionization) is tested due to the recently attracted interest. The obtained results indicate that for the source Prometheus I, the dominant formation process is dissociative attachment.

  15. Interspecies Ion Diffusion Studies using DT, DT(3He), and DT(H) Implosions

    Science.gov (United States)

    Kim, Y.; Herrmann, H. W.; Schmitt, M. J.; Kagan, G.; McEvoy, A. M.; Hoffman, N. M.; Gales, S.; Leatherland, A.; Gatu Johnson, M.; Frenje, J.; Glevov, V. Yu; Forrest, C.

    2015-11-01

    Anomalous ICF yield degradation has been observed from gas fills containing mixtures (i.e., D(3He), DT(3He), D(Ar), and even DT). Interspecies ion diffusion theory has been suggested as a possible cause resulting from gradient-driven diffusion (i.e., pressure, electric potential, and temperature) which forces lower mass ions away from core and higher mass ions toward core. The theory predicts hydrogen addition to deuterium or tritium should result in increased yield compared to expected yield, which is opposite to 3He addition. At Omega laser facility, we have tested hydro-equivalent fills of DT, DT(3He), and DT(H) with the assumption that same fuel mass and particle pressure will provide identical convergence. Preliminary results verify a factor of 2 yield reduction relative to scaling when 3He added to DT. At DT(H) case, however, no significant yield degradation or a slight yield enhancement was observed which agrees with the interspecies ion diffusion theory. Detailed experiment results and simulation are needed to confirm the initial observation.

  16. Rotationally inelastic collisions of H2+ ions with He buffer gas: Computing cross sections and rates

    Science.gov (United States)

    Hernández Vera, Mario; Gianturco, F. A.; Wester, R.; da Silva, H.; Dulieu, O.; Schiller, S.

    2017-03-01

    We present quantum calculations for the inelastic collisions between H2+ molecules, in rotationally excited internal states, and He atoms. This work is motivated by the possibility of experiments in which the molecular ions are stored and translationally cooled in an ion trap and a He buffer gas is added for deactivation of the internal rotational population, in particular at low (cryogenic) translational temperatures. We carry out an accurate representation of the forces at play from an ab initio description of the relevant potential energy surface, with the molecular ion in its ground vibrational state, and obtain the cross sections for state-changing rotationally inelastic collisions by solving the coupled channel quantum scattering equations. The presence of hyperfine and fine structure effects in both ortho- and para-H2+ molecules is investigated and compared to the results where such a contribution is disregarded. An analysis of possible propensity rules that may predict the relative probabilities of inelastic events involving rotational state-changing is also carried out, together with the corresponding elastic cross sections from several initial rotational states. Temperature-dependent rotationally inelastic rates are then computed and discussed in terms of relative state-changing collisional efficiency under trap conditions. The results provide the essential input data for modeling different aspects of the experimental setups which can finally produce internally cold molecular ions interacting with a buffer gas.

  17. Directional effect on coloration in LiF crystal by H{sup +} and H{sub 2}{sup +} ion bombardment

    Energy Technology Data Exchange (ETDEWEB)

    Gan Mingle; Naramoto, Hiroshi; Aoki, Yasushi; Yamamoto, Shunya; Zeng Jianer; Takeshita, Hidefumi [Japan Atomic Energy Research Inst., Takasaki, Gunma (Japan). Takasaki Radiation Chemistry Research Establishment

    1997-03-01

    In the present paper, the first results are reported about the coloration in LiF crystals induced by bombardments of single hydrogen ions (H{sup +}) and molecular hydrogen ions (H{sub 2}{sup +}) with the same velocity under the <100> aligned and random conditions. For the single hydrogen ion irradiation, the coloration is rather simple. The F-type color center absorption under the <100> aligned condition becomes larger than that under the random condition with the dose increase because of larger fraction of electronic energy loss under channeling condition. On the contrary, the coloration for the molecular ions does not show big channeling effect. In the low dose region some difference can be seen but the difference of coloration is not observed any more with the dose increase. The pronounced coloration for molecular ions under the channeling condition is observed in comparison with that for single ions. (author)

  18. Optical waveguides in Nd:GGG crystals produced by H+ or C3+ ion implantation.

    Science.gov (United States)

    Ren, Ying-Ying; Chen, Feng; Lu, Qing-Ming; Ma, Hong-Ji

    2010-04-10

    The optical waveguides in neodymium-doped gadolinium gallium garnet crystal are fabricated, to our knowledge for the first time, by either H(+) or C(3+) ion implantation. The reconstructed refractive index profiles of the planar waveguides have shown, in both cases, the typical "enhanced well" + "barrier" distributions. The two-dimensional modal profiles of the channel waveguides, obtained by using an end-face coupling arrangement, are in good agreement with the simulated modal distributions. After moderate thermal annealing at 200 degrees C, the propagation loss of the H- and C-ion-implanted channel waveguides are reduced down to approximately 1.5 and approximately 1.6 dB/cm, respectively, which exhibits acceptable guiding qualities for applications on potential integrated laser generation.

  19. Change of pH and Iron Ion Concentration During Photodegradation of TCE with Ferrioxalate/UVvis Process

    Science.gov (United States)

    Hareyama, Wataru; Suto, Koichi; Inoue, Chihiro; Chida, Tadashi; Nakazawa, Hiroshi

    2006-05-01

    Recently, some studies show various organic compounds such as pesticides and dyes degraded with the irradiation of ultraviolet light and visible light in the presence of oxalic acid and ferric ion (ferrioxalate/UVvis process). The process has much advance than other technologies because it can utilize the wavelength of 300˜450nm and also under the condition of neutral pH. Chlorinated organic compounds such as trichloroethene (TCE), which have caused ground water pollution on a lot of sites, have never been applied by photodegradation with this process. In this study, we showed the degradation of TCE in the presence of oxalic acid and iron ion and the change of pH, ferric and ferrous ion concentration during the photodegradation of TCE with ferrioxalate/UV-vis process. TCE was degraded in the presence of oxalic acid and iron ion. In the reactions, the equilibrium of oxalate ion and iron ion is important since it determines the amount of ferrioxalate complex which absorbs light and induces the reactions of the degradation of TCE. Thus, the pH value and iron ion concentration are the important factors which determine the amount of ferrioxalate complex. The pH is nearly constant during the photodegradation of TCE. The ferrous ion concentration was decreased as soon as beginning photodegradation of TCE, and then the ferrous ion concentration and ferric ion concentration became constant.

  20. Negative hydrogen ion sources for accelerators

    Energy Technology Data Exchange (ETDEWEB)

    Moehs, D.P.; /Fermilab; Peters, J.; /DESY; Sherman, J.; /Los Alamos

    2005-08-01

    A variety of H{sup -} ion sources are in use at accelerator laboratories around the world. A list of these ion sources includes surface plasma sources with magnetron, Penning and surface converter geometries as well as magnetic-multipole volume sources with and without cesium. Just as varied is the means of igniting and maintaining magnetically confined plasmas. Hot and cold cathodes, radio frequency, and microwave power are all in use, as well as electron tandem source ignition. The extraction systems of accelerator H{sup -} ion sources are highly specialized utilizing magnetic and electric fields in their low energy beam transport systems to produce direct current, as well as pulsed and/or chopped beams with a variety of time structures. Within this paper, specific ion sources utilized at accelerator laboratories shall be reviewed along with the physics of surface and volume H{sup -} production in regard to source emittance. Current research trends including aperture modeling, thermal modeling, surface conditioning, and laser diagnostics will also be discussed.

  1. Measurement of diffusion coefficient of thallium ion in H2O and D2O systems at different concentrations

    International Nuclear Information System (INIS)

    Das, A.; Changdar, S.N.

    1992-01-01

    Sliding cell method, developed in our laboratory, has been used to measure the inter diffusion coefficient of thallium ion in thallous sulphate solution over a wide concentration range using both water and heavy water as solvent at 35degC. The results have been analysed from the point of view of both ion-ion and ion-solvent interactions. The comparison of the diffusivities of the same ion in D 2 O and H 2 O electrolyte solutions at the same temperature indicate that the addition of salt affects the two solvent differently. (author). 8 refs., 1 fig., 1 tab

  2. Impact of He and H relative depth distributions on the result of sequential He+ and H+ ion implantation and annealing in silicon

    Science.gov (United States)

    Cherkashin, N.; Daghbouj, N.; Seine, G.; Claverie, A.

    2018-04-01

    Sequential He++H+ ion implantation, being more effective than the sole implantation of H+ or He+, is used by many to transfer thin layers of silicon onto different substrates. However, due to the poor understanding of the basic mechanisms involved in such a process, the implantation parameters to be used for the efficient delamination of a superficial layer are still subject to debate. In this work, by using various experimental techniques, we have studied the influence of the He and H relative depth-distributions imposed by the ion energies onto the result of the sequential implantation and annealing of the same fluence of He and H ions. Analyzing the characteristics of the blister populations observed after annealing and deducing the composition of the gas they contain from FEM simulations, we show that the trapping efficiency of He atoms in platelets and blisters during annealing depends on the behavior of the vacancies generated by the two implants within the H-rich region before and after annealing. Maximum efficiency of the sequential ion implantation is obtained when the H-rich region is able to trap all implanted He ions, while the vacancies it generated are not available to favor the formation of V-rich complexes after implantation then He-filled nano-bubbles after annealing. A technological option is to implant He+ ions first at such an energy that the damage it generates is located on the deeper side of the H profile.

  3. Origin of CH+ in diffuse molecular clouds. Warm H2 and ion-neutral drift

    Science.gov (United States)

    Valdivia, Valeska; Godard, Benjamin; Hennebelle, Patrick; Gerin, Maryvonne; Lesaffre, Pierre; Le Bourlot, Jacques

    2017-04-01

    Context. Molecular clouds are known to be magnetised and to display a turbulent and complex structure where warm and cold phases are interwoven. The turbulent motions within molecular clouds transport molecules, and the presence of magnetic fields induces a relative velocity between neutrals and ions known as the ion-neutral drift (vd). These effects all together can influence the chemical evolution of the clouds. Aims: This paper assesses the roles of two physical phenomena which have previously been invoked to boost the production of CH+ under realistic physical conditions: the presence of warm H2 and the increased formation rate due to the ion-neutral drift. Methods: We performed ideal magnetohydrodynamical (MHD) simulations that include the heating and cooling of the multiphase interstellar medium (ISM), and where we treat dynamically the formation of the H2 molecule. In a post-processing step we compute the abundances of species at chemical equilibrium using a solver that we developed. The solver uses the physical conditions of the gas as input parameters, and can also prescribe the H2 fraction if needed. We validate our approach by showing that the H2 molecule generally has a much longer chemical evolution timescale compared to the other species. Results: We show that CH+ is efficiently formed at the edge of clumps, in regions where the H2 fraction is low (0.3-30%) but nevertheless higher than its equilibrium value, and where the gas temperature is high (≳ 300 K). We show that warm and out of equilibrium H2 increases the integrated column densities of CH+ by one order of magnitude up to values still 3-10 times lower than those observed in the diffuse ISM. We balance the Lorentz force with the ion-neutral drag to estimate the ion-drift velocities from our ideal MHD simulations. We find that the ion-neutral drift velocity distribution peaks around 0.04 km s-1, and that high drift velocities are too rare to have a significant statistical impact on the

  4. Ion-exchange synthesis and improved Li insertion property of lithiated H2Ti12O25 as a negative electrode material for lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Kunimitsu Kataoka

    2016-03-01

    Full Text Available We successfully prepared the lithiated H2Ti12O25 sample by the H+/Li+ ion exchange synthetic technique in the molten LiNO3 at 270 °C using H2Ti12O25 as a starting compound. Chemical composition of the obtained lithiated H2Ti12O25 sample was determined to be H1.05Li0.35Ti12O25-δ having δ = 0.3 by ICP-AES and DTA-TG analyses. The H+/Li+ ion exchange was also confirmed by powder XRD, 1H-MAS NMR, and 7Li-MAS NMR measurements. Electrochemical Li insertion and extraction measurements revealed that the initial coulombic efficiency was improved from 88% in H2Ti12O25 to 93% in the lithiated H2Ti12O25 sample. In addition, superior capacity retention properties for the charge and discharge cycling performance and good charge rate capability of the present lithiated H2Ti12O25 were confirmed in the electrochemical measurements. Accordingly, the lithiated H2Ti12O25 is suggested to be one of the promising high-voltage and high-capacity oxide negative electrodes in advanced lithium-ion batteries.

  5. Synergistic effects of iodine and silver ions co-implanted in 6H-SiC

    Science.gov (United States)

    Kuhudzai, R. J.; Malherbe, J. B.; Hlatshwayo, T. T.; van der Berg, N. G.; Devaraj, A.; Zhu, Z.; Nandasiri, M.

    2015-12-01

    Motivated by the aim of understanding the release of fission products through the SiC coating of fuel kernels in modern high temperature nuclear reactors, a fundamental investigation is conducted to understand the synergistic effects of implanted silver (Ag) and iodine (I) in 6H-SiC. The implantation of the individual species, as well as the co-implantation of 360 keV ions of I and Ag at room temperature in 6H-SiC and their subsequent annealing behaviour has been investigated by Secondary Ion Mass Spectrometry (SIMS), Atom Probe Tomography (APT) and X-ray Photoelectron Spectroscopy (XPS). SIMS and APT measurements indicated the presence of Ag in the co-implanted samples after annealing at 1500 °C for 30 h in sharp contrast to the samples implanted with Ag only. In samples implanted with Ag only, complete loss of the implanted Ag was observed. However, for I only implanted samples, some iodine was retained. APT of annealed co-implanted 6H-SiC showed clear spatial association of Ag and I clusters in SiC, which can be attributed to the observed I assisted retention of Ag after annealing. Such detailed studies will be necessary to identify the fundamental mechanism of fission products migration through SiC coatings.

  6. Influence of the cusp field on the plasma parameters of the Linac4 H- ion source

    Science.gov (United States)

    Briefi, S.; Mattei, S.; Lettry, J.; Fantz, U.

    2017-08-01

    When the H- ion source of CERN's Linac4 is operated in volume mode, a maximum of the extracted current is obtained at varying RF power. The power required for this maximum and its absolute value is strongly influenced by the cusp magnets installed at the source for electron confinement: without magnets, 15-20 mA are typically obtained at 20 kW whereas with magnets a factor of two more power is needed and 25-30 mA are achieved. In order to access the reasons behind the peaked performance with varying RF power and for determining the influence of the cusp field on the discharge, optical emission spectroscopy (OES) measurements of the atomic Balmer series and of the molecular Fulcher transition have been carried out. In all investigated cases, the gas temperature of the discharge has been virtually equal to the ambient temperature as the short discharge pulse length of 500 µs is not long enough for considerable heavy particle heating. When no cusp magnets are installed, the plasma parameters evaluated with the collisional radiative models Yacora H and Yacora H2 show a minimum in the electron temperature of 3.25 eV and a maximum in the electron density of 4×1019 m-3 and also in the vibrational excitation of the hydrogen molecule at 20 kW. Assessing the relevant production and destruction processes demonstrates that the H- yield is maximal at this point thereby explaining the optimum ion source performance. When the cusp magnets are applied, the same general trends are observed but the required RF power is a factor of two higher. The OES results indicate an optimum performance around 30 kW whereas the highest H- current is actually achieved around 40 kW. Furthermore, a higher H- yield is indicated without cusp magnets but a better ion source performance is observed with magnets. These differences can most likely be attributed to changing gradients in the plasma parameters which are not accessible by OES. Nevertheless, the obtained plasma parameters can be used as

  7. Improvements to the internal and external antenna H(-) ion sources at the Spallation Neutron Source.

    Science.gov (United States)

    Welton, R F; Dudnikov, V G; Han, B X; Murray, S N; Pennisi, T R; Pillar, C; Santana, M; Stockli, M P; Turvey, M W

    2014-02-01

    The Spallation Neutron Source (SNS), a large scale neutron production facility, routinely operates with 30-40 mA peak current in the linac. Recent measurements have shown that our RF-driven internal antenna, Cs-enhanced, multi-cusp ion sources injects ∼55 mA of H(-) beam current (∼1 ms, 60 Hz) at 65-kV into a Radio Frequency Quadrupole (RFQ) accelerator through a closely coupled electrostatic Low-Energy Beam Transport system. Over the last several years a decrease in RFQ transmission and issues with internal antennas has stimulated source development at the SNS both for the internal and external antenna ion sources. This report discusses progress in improving internal antenna reliability, H(-) yield improvements which resulted from modifications to the outlet aperture assembly (applicable to both internal and external antenna sources) and studies made of the long standing problem of beam persistence with the external antenna source. The current status of the external antenna ion source will also be presented.

  8. Experimental study of high current negative ion sources D- / H-. Analysis based on the simulation of the negative ion transport in the plasma source

    International Nuclear Information System (INIS)

    Riz, D.

    1996-01-01

    In the frame of the development of a neutral beam injection system able to work the ITER tokamak (International Thermonuclear Experimental Reactor), two negative ion sources, Dragon and Kamaboko, have been installed on the MANTIS test bed in Cadarache, and studies in order to extract 20 mA/cm 2 of D - . The two production modes of negative ions have been investigated: volume production; surface production after cesium injection in the discharge. Experiments have shown that cesium seeding is necessary in order to reach the requested performances for ITER. 20 mA/cm 2 have been extracted from the Kamaboko source for an arc power density of 2.5 kW/liter. Simultaneously, a code called NIETZSCHE has been developed to simulate the negative ions transport in the source plasma, from their birth place to the extraction holes. The ion trajectory is calculated by numerically solving the 3D motion equation, while the atomic processes of destruction, of elastic collisions H - /H + and of charge exchange H - /H 0 are handled at each time step by a Monte Carlo procedure. The code allows to obtain the extraction probability of a negative ion produced at a given location. The calculations performed with NIETZSCHE have allowed to explain several phenomena observed on negative ion sources, such as the isotopic effect H - /D - and the influence of the polarisation of the plasma grid and of the magnetic filter on the negative ions current. The code has also shown that, in the type of sources contemplated for ITER, working with large arc power densities (> 1 kW/liter), only negative ions produced in volume at a distance lower that 2 cm from the plasma grid and those produced at the grid surface have a chance of being extracted. (author)

  9. Modifications in physico-chemical properties of 100 MeV oxygen ions irradiated polyimide Kapton-H polymer

    Science.gov (United States)

    Gupta, Sanjeev Kumar; Gupta, Rashi; Singh, Paramjit; Kumar, Vikas; Jaiswal, Manoj Kumar; Chakarvarti, S. K.; Kumar, Rajesh

    2017-09-01

    The optical, structural and chemical properties of polyimide Kapton-H polymer thin film samples were modified by irradiation with 100 MeV O7+ ions (in the fluence range of 1 × 1011 to 5 × 1012 ions/cm2) and the modifications of these properties were observed by UV-visible (UV-Vis) spectroscopy, X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy respectively. The band gap energy of the polymer decreased considerably with discrete increment of the ion fluence (different fluence for each sample) and effective change for the sample irradiated at a fluence of 5 × 1012 ions/cm2 was observed from that of pristine sample. The amorphous nature of the polymer was observed to be decreased with increase of ion fluence. The vibrations of Ctbnd C appeared at mid fluences but the stretching vibrations of Osbnd H bond disappeared at these fluences due to the high LET of the oxygen ions.

  10. H2O2 Synthesis Induced by Irradiation of H2O with Energetic H(+) and Ar(+) Ions at Various Temperatures

    Science.gov (United States)

    Baragiola, R. A.; Loeffler, M. J.; Raut, U.; Vidal, R. A.; Carlson, R. W.

    2004-01-01

    The detection of H2O2 on Jupiter's icy satellite Europa by the Galileo NIMS instrument presented a strong evidence for the importance of radiation effects on icy surfaces. A few experiments have investigated whether solar flux of protons incident on Europa ice could cause a significant if any H2O2 production. These published results differ as to whether H2O2 can be formed by ions impacting water at temperatures near 80 K, which are appropriate to Europa. This discrepancy may be a result of the use of different incident ion energies, different vacuum conditions, or different ways of processing the data. The latter possibility comes about from the difficulty of identifying the 3.5 m peroxide OH band on the long wavelength wing of the much stronger water 3.1 m band. The problem is aggravated by using straight line baselines to represent the water OH band with a curvature, in the region of the peroxide band, that increases with temperature. To overcome this problem, we use polynomial baselines that provide good fits to the water band and its derivative.

  11. Electron collisions with the BeH{sup +} molecular ion in the R-matrix approach

    Energy Technology Data Exchange (ETDEWEB)

    Chakrabarti, K. [Department of Mathematics, Scottish Church College, 1-3 Urquhart Sq., 700006 Kolbata (India); Tennyson, J. [Department of Physicas and Astronomy, University College London, Gower Street, WC1E 6BT London (United Kingdom)

    2012-01-15

    BeH{sup +} is formed when fusion plasma interacts with beryllium first walls, so the interaction of electrons in the plasma with BeH{sup +} needs to be understood. The R-matrix method is used to study electron collisions with the BeH{sup +} molecular ion. The diatomic version of the UK Molecular R-matrix codes is used and a configuration-interaction calculation is first performed for the BeH{sup +} target to obtain its potential energy curves for 19 lowest singlet and triplet states. Scattering calculations are then done to yield excitation and rotational excitation cross sections in the energy range 0 - 14 eV. Additionally we also obtain bound states of BeH and their quantum defects at the BeH equilibrium bond length 2.5369*a{sub 0}. Resonance positions and widths for Feshbach resonances in the e-BeH{sup +} system are also obtained and presented at the equilibrium bond length 2.5369*a{sub 0}

  12. Temperature dependence of binary and ternary recombination of H3+ ions with electrons

    International Nuclear Information System (INIS)

    Glosik, J.; Plasil, R.; Korolov, I.; Kotrik, T.; Novotny, O.; Hlavenka, P.; Dohnal, P.; Varju, J.; Kokoouline, V.; Greene, Chris H.

    2009-01-01

    We study binary and the recently discovered process of ternary He-assisted recombination of H 3 + ions with electrons in a low-temperature afterglow plasma. The experiments are carried out over a broad range of pressures and temperatures of an afterglow plasma in a helium buffer gas. Binary and He-assisted ternary recombination are observed and the corresponding recombination rate coefficients are extracted for temperatures from 77 to 330 K. We describe the observed ternary recombination as a two-step mechanism: first, a rotationally excited long-lived neutral molecule H 3 * is formed in electron-H 3 + collisions. Second, the H 3 * molecule collides with a helium atom that leads to the formation of a very long-lived Rydberg state with high orbital momentum. We present calculations of the lifetimes of H 3 * and of the ternary recombination rate coefficients for para- and ortho-H 3 + . The calculations show a large difference between the ternary recombination rate coefficients of ortho- and para-H 3 + at temperatures below 300 K. The measured binary and ternary rate coefficients are in reasonable agreement with the calculated values.

  13. Temperature dependence of binary and ternary recombination of H3+ ions with electrons

    Science.gov (United States)

    Glosík, J.; Plašil, R.; Korolov, I.; Kotrík, T.; Novotný, O.; Hlavenka, P.; Dohnal, P.; Varju, J.; Kokoouline, V.; Greene, Chris H.

    2009-05-01

    We study binary and the recently discovered process of ternary He-assisted recombination of H3+ ions with electrons in a low-temperature afterglow plasma. The experiments are carried out over a broad range of pressures and temperatures of an afterglow plasma in a helium buffer gas. Binary and He-assisted ternary recombination are observed and the corresponding recombination rate coefficients are extracted for temperatures from 77 to 330 K. We describe the observed ternary recombination as a two-step mechanism: first, a rotationally excited long-lived neutral molecule H3∗ is formed in electron- H3+ collisions. Second, the H3∗ molecule collides with a helium atom that leads to the formation of a very long-lived Rydberg state with high orbital momentum. We present calculations of the lifetimes of H3∗ and of the ternary recombination rate coefficients for para- and ortho- H3+ . The calculations show a large difference between the ternary recombination rate coefficients of ortho- and para- H3+ at temperatures below 300 K. The measured binary and ternary rate coefficients are in reasonable agreement with the calculated values.

  14. 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

  15. Charge spectrum of positive ions in a hydrogen aurora. [H/sup +/, He/sup + +/, O/sup +/

    Energy Technology Data Exchange (ETDEWEB)

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

    1976-03-01

    An auroral ion charge spectrometer was flown into a hydrogen aurora on a Javelin sounding rocket launched from Churchill, Manitoba. The instrument contained an electrostatic analyzer which selected particles with incident energy per unit charge up to 20 keV/charge and an 80-kV power supply which accelerated these ions onto an array of solid state detectors. Ions tentatively identified as H/sup +/, He/sup + +/, and O/sup +/ were detected from 225 to 820 km in altitude. The experiment did not discriminate between H/sup +/ and He/sup +/, or between O/sup +/, N/sup +/, and C/sup +/. Upper limits of highly charged heavy ion abundances have been set at 20% of the He/sup + +/ and 0.15% of the H/sup +/. It is concluded that both terrestrial and solar wind sources play significant roles in auroral ion precipitation. (AIP)

  16. Operational experience with the TRIUMF optically pumped polarized H- ion source

    International Nuclear Information System (INIS)

    Schmor, P.W.; Buchmann, L.; Jayamanna, K.; Levy, C.D.P.; McDonald, M.; Ruegg, R.

    1991-05-01

    The initial goal of a polarized proton beam extracted from the TRIUMF cyclotron, having a current of 5 μA with 60% polarization, has been achieved with the development of the optically pumped polarized H - ion source. This beam is now being used to produce an intense secondary beam of polarized neutrons for the TRIUMF experimental program. Much of the recent development effort has addressed the reliability requirements for routine operation. This paper describes the results with emphasis on the laser stabilization subsystem, the modifications to the electron cyclotron resonance proton ion source (ECRIS), the sodium charge exchange cells and the development of a low energy polarimeter. Also discussed are the developments which should lead to a higher polarization. (Author) 7 refs

  17. Plasma ignition and steady state simulations of the Linac4 H$^{-}$ ion source

    CERN Document Server

    Mattei, S; Yasumoto, M; Hatayama, A; Lettry, J; Grudiev, A

    2014-01-01

    The RF heating of the plasma in the Linac4 H- ion source has been simulated using an Particle-in-Cell Monte Carlo Collision method (PIC-MCC). This model is applied to investigate the plasma formation starting from an initial low electron density of 1012 m-3 and its stabilization at 1018 m-3. The plasma discharge at low electron density is driven by the capacitive coupling with the electric field generated by the antenna, and as the electron density increases the capacitive electric field is shielded by the plasma and induction drives the plasma heating process. Plasma properties such as e-/ion densities and energies, sheath formation and shielding effect are presented and provide insight to the plasma properties of the hydrogen plasma.

  18. FTIR and Raman spectra of ion irradiated and annealed 4H-SiC

    International Nuclear Information System (INIS)

    Zhou Lihong; Yang Titao; Yao Cunfeng; Chinese Academy of Sciences, Beijing

    2007-01-01

    The 4H-SiC specimens were implanted with 110keV C-ions and then irradiated with 230MeV Pb-ions and subsequently annealed at different temperatures in vacuum. The samples were investigated after each annealing stage by using FTIR and Raman spectroscopy. The obtained FTIR spectra showed several interference fringes in the range from 960 cm -1 to 1450 cm -1 . The intensity of fringes decreases with the increase of annealing temperature, and an abrupt decrease of the fringe intensity was found for annealing above 900 degree C, indicating that there was a significant recovery of the irradiation-induced damage in the crystal for annealing at high temperatures. The Raman spectroscopy showed that after annealing at 1200 degree C for 30 min the amorphous layer was recovered and the precipitation of carbon atoms in graphite occurred. (authors)

  19. CINETIQUE DES IONS PHOSPHORIQUES H2PO4- ET HPO4-2 EN MILIEU GYPSEUX

    Directory of Open Access Journals (Sweden)

    Hacène BOUZIANE

    2011-06-01

    Full Text Available L’étude de la fixation des ions H2PO4- et HPO4-2 par les divers types de gypse (tassé ; feuilleté ; fibreux. Donne une réaction positive quelle que soit la solution phosphaté et le type de gypse utilisé. Il convient de noter que l’adsorption est beaucoup plus forte pour les ions H2PO4- que celle des ions HPO4-2 et qu’elle varie d’un type de gypse à l’autre.                 L’étude de l’influence du temps, de la granulométrie et de la concentration des solutions montrent en effet que : plus le diamètre du grain est petit, plus l’adsorption est forte. La fixation se produit même pour une solution phosphatée à très faible concentration ; il se produit toujours une réaction avec précipitation et non un équilibre d’adsorption. La réaction des ions phosphatés augment rapidement dans les premières minutes quel que soit le type de gypse et la concentration utilisée. Nous avons abouti à la formation d’un gel phosphaté, visqueux et non soluble. L’analyse chimique de ce gel donne les résultats suivants : PO4=54,20% ,Ca=11,30% , K=32,94%; si l’on compare ces résultats avec les résultats calculés pour K3CaH,(PO42=PO4=54,59%, Ca=11,19%, K=33,62%, nos valeurs sont très voisines de celles-ci. Il s’agit donc du même sel sur lequel aucun travail sur la formation de K3CaH(PO42 à partir de CaSO42H2O ne semble avoir été publié.

  20. Structural transitions, ion mobility, and conductivity in CsSbF3(H2PO4)

    Science.gov (United States)

    Kavun, V. Ya.; Uvarov, N. F.; Slobodyuk, A. B.; Ulihin, A. S.; Kovaleva, E. V.; Zemnukhova, L. A.

    2018-02-01

    Structural transitions, ion mobility, and conductivity in CsSbF3(H2PO4) (I) have been investigated by the methods of 1H, 19F, 31P NMR (including 1H, 19F, 31P MAS NMR), DSC, X-ray diffraction, and impedance spectroscopy. It was found that the fundamental changes in 1H, 19F, 31P NMR spectra (above 390 K) were associated with the formation of a crystalline disorder phase I with high ionic mobility in the proton and fluoride sublattices, as a result of a phase transition in the 400-420 K range. In the same temperature range, the transition of PO2(OH)2- anions from the "rigid lattice" to fast reorientations takes place. Above 430 K, there occurs a transition from the crystalline disordered phase to the amorphous one. The types of ion mobility in CsSbF3(H2PO4) and its amorphous phase have been established and temperature ranges of their realization have been determined (150-450 K). According to the NMR data, the diffusion in the proton sublattice of the disordered crystalline and amorphous phases is preserved even at room temperature. The ionic conductivity in CsSbF3(H2PO4) reaches the values of 2.6 × 10-4 S/cm in the temperature range 410-425 K and decreases down to 2.0 × 10-5 S/cm upon transition to the amorphous phase (435-445 K).

  1. Allotropic effects on the energy loss of swift H+ and He+ ion beams through thin foils

    International Nuclear Information System (INIS)

    Garcia-Molina, Rafael; Abril, Isabel; Denton, Cristian D.; Heredia-Avalos, Santiago

    2006-01-01

    We have developed a theoretical treatment and a simulation code to study the energy loss of swift H + and He + ion beams interacting with thin foils of different carbon allotropes. The former is based on the dielectric formalism, and the latter combines Monte Carlo with the numerical solution of the motion equation for each projectile to describe its trajectory and interactions through the target. The capabilities of both methods are assessed by the reasonably good agreement between their predictions and the experimental results, for a wide range of projectile energies and target characteristics. Firstly, we apply the theoretical procedure to calculate the stopping cross sections for H + and He + beams in foils of different allotropic forms of carbon (such as diamond, graphite, amorphous carbon, glassy carbon and C 60 -fullerite), as a function of the projectile energy. We take into account the electronic structure of the projectile, as well as the different charge states it can acquire, the energy loss associated to the electronic capture and loss processes, the polarization of the projectile, and a realistic description of the target. On the other hand, the simulation code is used to evaluate the energy distributions of swift H + and He + ion beams when traversing several foils of the above mentioned allotropic forms of carbon, in order to analyze the influence of the chemical and physical state of the target in the projectile energy loss. These allotropic effects are found to become more important around the maximum of the stopping cross-section

  2. Modeling of pH Dependent Electrochemical Noise in Ion Sensitive Field Effect Transistors ISFET

    Directory of Open Access Journals (Sweden)

    M. P. Das

    2013-02-01

    Full Text Available pH ISFETs are very important sensor for in vivo continuous monitoring application of physiological and environmental system. The accuracy of Ion Sensitive Field Effect Transistor (ISFET output measurement is greatly affected by the presences of noise, drift and slow response of the device. Although the noise analysis of ISFET so far performed in different literature relates only to sources originated from Field Effect Transistor (FET structure which are almost constant for a particular device, the pH dependent electrochemical noise has not been substantially explored and analyzed. In this paper we have investigated the low frequency pH dependent electrochemical noise that originates from the ionic conductance of the electrode-electrolyte-Field Effect Transistor structure of the device and that the noise depends on the concentration of the electrolyte and 1/f in nature. The statistical and frequency analysis of this electrochemical noise of a commercial ISFET sensor, under room temperature has been performed for six different pH values ranging from pH2 to pH9.2. We have also proposed a concentration dependent a/f & b/f2 model of the noise with different values of the coefficients a, b.

  3. Influence of H2 reduction on lignin-based hard carbon performance in lithium ion batteries

    International Nuclear Information System (INIS)

    Chang, Zhen-zhen; Yu, Bao-jun; Wang, Cheng-yang

    2015-01-01

    ABSTRACT: Lignin as a by-product of fuel alcohol industry is used to prepare hard carbon materials by acetone extraction, stabilization in N 2 at 300 °C, carbonization in N 2 and subsequent H 2 reduction at 800 °C. The effect of H 2 reduction after carbonization process on the performances of the prepared samples is systematically studied and a simple mechanism is proposed. Excitingly, it is demonstrated that the process of H 2 reduction has a favorable influence on both structures and electrochemical performances of pyrolysis sample and an obvious improvement of capacity performance is obtained with reduction treatment. A first discharge/ charge capacity of 882.2/550.5 mA h g −1 (coulombic efficiency (CE) of 62.4%) is achieved at 0.1 C (1C = 372 mA g −1 ), and even after 200 cycles at 2 C a charge capacity of 228.8 mA h g −1 (about 92.8% retention ratio) remains and CE is above 99% during cycles for H 2 reduced sample. The fabulous electrochemical performance could be attributed to high purity of acetone-extracted lignin, low surface oxygen-containing functional groups and relatively high graphitization degree of reduction sample. In a word, both the simple pyrolysis process and excellent electrochemical performance make lignin-based hard carbon a promising anode material for high-capacity and high-stability lithium ion batteries (LIBs)

  4. The average equilibrium charge-states of heavy ions with Z > 60 stripped in He and H2

    International Nuclear Information System (INIS)

    Oganessian, Yu.T.; Lobanov, Yu.V.; Popeko, A.G.; Abdullin, F.Sh.; Kharitonov, Yu.P.; Ledovskoy, A.A.; Tsyganov, Yu.S.

    1991-01-01

    The equilibrium charges of heavy ions (61 < Z < 101) with energies from 5 to 100 MeV stripped in He and H2 have been measured. New empirical formulae for the average charge state are presented. (orig.)

  5. Spectroscopic measurement of H(1S) and H sub 2 (v double prime ,J double prime ) in an H sup minus ion source plasma

    Energy Technology Data Exchange (ETDEWEB)

    Stutzin, G.C.

    1990-08-01

    Low pressure H{sub 2} discharges have been used for some time as sources of H{sup {minus}} ions. These discharges contain many different species of particles which interact with each other and with the walls of the discharge chamber. Models exist that predict the populations of the various species for given macroscopic discharge parameters. However, many of the cross sections and wall catalyzation coefficients are unknown or somewhat uncertain. Therefore, it is of interest to measure the populations of as many of these species as possible, in order to determine the validity of the models. These models predict that H{sup {minus}} is created predominantly by the two-step process of vibrational excitation of hydrogen molecules followed by dissociative attachment of slow electrons to these vibrationally-excited hydrogen molecules. Many different collisional processes must be included in the models to explain the dependence of the various populations upon macroscopic parameters. This work presents results of spectroscopic measurements of the density and translational temperature of hydrogen atoms and of specific rotationally- and vibrationally-excited states of electronic ground-state H{sub 2}, in a discharge optimized for H{sup {minus}} production, as well as conventional measurements of the various charged species within the plasma. The spectroscopic measurements are performed directly by narrowband, single-photon absorption in the vacuum ultraviolet.

  6. Spectroscopic measurement of H(1S) and H2(v double-prime,J double-prime) in an H- ion source plasma

    International Nuclear Information System (INIS)

    Stutzin, G.C.

    1990-08-01

    Low pressure H 2 discharges have been used for some time as sources of H - ions. These discharges contain many different species of particles which interact with each other and with the walls of the discharge chamber. Models exist that predict the populations of the various species for given macroscopic discharge parameters. However, many of the cross sections and wall catalyzation coefficients are unknown or somewhat uncertain. Therefore, it is of interest to measure the populations of as many of these species as possible, in order to determine the validity of the models. These models predict that H - is created predominantly by the two-step process of vibrational excitation of hydrogen molecules followed by dissociative attachment of slow electrons to these vibrationally-excited hydrogen molecules. Many different collisional processes must be included in the models to explain the dependence of the various populations upon macroscopic parameters. This work presents results of spectroscopic measurements of the density and translational temperature of hydrogen atoms and of specific rotationally- and vibrationally-excited states of electronic ground-state H 2 , in a discharge optimized for H - production, as well as conventional measurements of the various charged species within the plasma. The spectroscopic measurements are performed directly by narrowband, single-photon absorption in the vacuum ultraviolet

  7. Laser-stimulated electric quadrupole transitions in the molecular hydrogen ion H2+

    Science.gov (United States)

    Korobov, V. I.; Danev, P.; Bakalov, D.; Schiller, S.

    2018-03-01

    Molecular hydrogen ions are of metrological relevance due to the possibility of precise theoretical evaluation of their spectrum and of external-field-induced shifts. We report the results of the calculations of the rate of laser-induced electric quadrupole transitions between a large set of ro-vibrational states of H2+. The hyperfine and Zeeman structure of the E 2 transition spectrum and the effects of the laser polarization are treated in detail. The treatment is generally applicable to molecules in 2Σ states. We also present the nuclear spin-electron spin-coupling constants, computed with a precision ten times higher than previously obtained.

  8. Fast Heavy Ion Collisions with H2 Molecules And Young Type Interference

    Science.gov (United States)

    Tribedi, Lokesh C.; Misra, Deepankar

    2007-12-01

    We have investigated the Young type interference effect in electron emission spectrum from molecular H2 in Coulomb ionization induced by fast heavy ions. The details of the derivation of the oscillations due to this process from the electron double differential distributions are discussed. In addition, we have explored the effect of Compton profile, on such interference oscillations, which gives rise a double-peak structure in case of low energy collisions for which the binary encounter peak starts overlapping with soft collision electrons. The measured DDCS as well as the interference patterns are compared with molecular CDW-EIS models.

  9. Effect of H + ion implantation on structural, morphological, optical and dielectric properties of L-arginine monohydrochloride monohydrate single crystals

    Science.gov (United States)

    Sangeetha, K.; Babu, R. Ramesh; Kumar, P.; Bhagvannarayana, G.; Ramamurthi, K.

    2011-06-01

    L-arginine monohydrochloride monohydrate (LAHCl) single crystals have been implanted with 100 keV H + ions at different ion fluence ranging from 10 12 to 10 15 ions/cm 2. Implanted LAHCl single crystals have been investigated for property changes. Crystal surface and crystalline perfection of the pristine and implanted crystals were analyzed by atomic force microscope and high-resolution X-ray diffraction studies, respectively. Optical absorption bands induced by colour centers, refractive index and birefringence, mechanical stability and dielectric constant of implanted crystals were studied at different ion fluence and compared with that of pristine LAHCl single crystal.

  10. The continued development of the Spallation Neutron Source external antenna H- ion source

    International Nuclear Information System (INIS)

    Welton, R. F.; Carmichael, J.; Fuga, R.; Goulding, R. H.; Han, B.; Kang, Y.; Lee, S. W.; Murray, S. N.; Pennisi, T.; Potter, K. G.; Santana, M.; Stockli, M. P.; Desai, N. J.

    2010-01-01

    The U.S. Spallation Neutron Source (SNS) is an accelerator-based, pulsed neutron-scattering facility, currently in the process of ramping up neutron production. In order to ensure that the SNS will meet its operational commitments as well as provide for future facility upgrades with high reliability, we are developing a rf-driven, H - ion source based on a water-cooled, ceramic aluminum nitride (AlN) plasma chamber. To date, early versions of this source have delivered up to 42 mA to the SNS front end and unanalyzed beam currents up to ∼100 mA (60 Hz, 1 ms) to the ion source test stand. This source was operated on the SNS accelerator from February to April 2009 and produced ∼35 mA (beam current required by the ramp up plan) with availability of ∼97%. During this run several ion source failures identified reliability issues, which must be addressed before the source re-enters production: plasma ignition, antenna lifetime, magnet cooling, and cooling jacket integrity. This report discusses these issues, details proposed engineering solutions, and notes progress to date.

  11. [Effects of thiourea on pH and availability of metal ions in acid red soil].

    Science.gov (United States)

    Yang, Bo; Wang, Wen; Zeng, Qing-Ru; Zhou, Xi-Hong

    2014-03-01

    Through the simulation research, the effects of application of thiourea and urea on pH and availability of metal ions in acid red soil were studied, and the results showed that after applying urea, the soil pH increased in the first experimental stage and then reduced gradually to a low level, however, decreased trends of soil pH values were inhibited by the application of thiourea, especially when the concentration of thiourea reached to 5.0 mmol x kg(-1) dry soil, the soil pH was stable at high level, which exceeded to 6.0. It proved that the application of thiourea could inhibit the soil acidification due to urea application. After applying urea with different concentrations of thiourea, the available contents of Zn and Al decreased with the increasing concentration of thiourea, nevertheless, when the concentration of thiourea reached to 5.0 mmol x kg(-1), the available content of Mn was stable at high level which was over 110 mg x kg(-1). In addition, the results showed a highly significant negative correlation between the soil pH and the available content of Cu, Zn and Al, but for Mn, no discipline was found between the soil pH and the availability after applying thiourea. Moreover, the soil pH became higher after applying urea with thiourea compared to add urea only, which led to the decreasing of available content of Al, and it was benefited for the control of the phytotoxic effect of Al. The available content of Mn in the soil not only depended on soil pH but also the content of thiourea due to its redox and complexing reaction with Mn.

  12. Measurements of the cesium flow from a surface-plasma H- ion source

    International Nuclear Information System (INIS)

    Smith, H.V.; Allison, P.W.

    1979-01-01

    A surface ionization gauge (SIG) was constructed and used to measure the Cs 0 flow rate through the emission slit of a surface-plasma source (SPS) of H - ions with Penning geometry. The equivalent cesium density in the SPS discharge is deduced from these flow measurements. For dc operation the optimum H - current occurs at an equivalent cesium density of approx. 7 x 10 12 cm -3 (corresponding to an average cesium consumption rate of 0.5 mg/h). For pulsed operation the optimum H - current occurs at an equivalent cesium density of approx. 2 x 10 13 cm -3 (1-mg/h average cesium consumption rate). Cesium trapping by the SPS discharge was observed for both dc and pulsed operation. A cesium energy of approx. 0.1 eV is deduced from the observed time of flight to the SIG. In addition to providing information on the physics of the source, the SIG is a useful diagnostic tool for source startup and operation

  13. Design of the Smart pH Sensor Based on Ion Selection Electrode

    Directory of Open Access Journals (Sweden)

    Xuelun Hu

    2014-03-01

    Full Text Available In aquaculture pH is one of the important indicators which affect cultivation objects’ healthy growth, whether pH value is normal or not would affect the survival of cultured objects. The traditional pH detecting method has poor stability and reliability, a smart pH sensor which is based on ion selective electrode has been designed in this paper, it adopts positive and negative double power to solve the problem of power supply, the self-excited prevented and impedance matching circuit has been designed to eliminate the self-excited oscillation circuit's influence on the measurement accuracy. The filter circuit has been designed to prevent the interference of the power frequency noise signal effectively, the zero and range adjustment circuit has been designed to expand the scope of the sensor. The temperature compensation correction model has been proposed to solve the problem of temperature compensation. The experiment results have shown that the developed sensor has good stability, reliability, and suitable for pH monitoring in aquaculture water quality.

  14. The influence of water pH and F- ions contamination in Zirconium alloys corrosion behaviour

    International Nuclear Information System (INIS)

    Radulescu, M.; Pirvan, I.

    1983-01-01

    The water chemistry of the primary circuit is one of the most important factors of influence on the corrosion behaviour in the PHWR of the fuel cladding materials: Zircaloy-2 and Zircaloy-4. We studied the influence of the water pH adjusted by LiOH. In this purpose were performed 3 days tests in lithiated water (pH: 10 - 13,5) at 360 deg. C and 180 bar on Zy-2 and Zy-4 samples. The gravimetric and micrographic results have shown that a LiOH concentration - ions as impurities in the primary circuit, we studied Zy-2 corrosion behaviour by 3 days tests in 1mg F - /l and 10mg F - /1 solutions, at 300 deg. C, 350 deg. C and 400 deg. C

  15. Monte Carlo solutions of Schroedinger's equation for H2+ ion in strong magnetic fields

    International Nuclear Information System (INIS)

    Ozaki, Jiro; Tomishima, Yasuo

    1980-01-01

    The analytical expressions suitable for the Monte Carlo calculation to obtain the solution of Schroedinger's equation of hydrogen molecular ion in a strong magnetic field are derived. The wave functions, the energy values and the equilibrium internuclear distances of 1σsub(g) state of H 2 + are obtained numerically through the Monte Carlo simulation and compared with other results based on the variational method. The agreement between them is fairly good over a wide range of magnetic field. The calculation of the energy values of 1πsub(g) state of H 2 + for various internuclear distances taking a constant magnetic field as a parameter, shows that the antibonding 1πsub(g) state in the absence of the external magnetic field changes to a bonding state with an increasing magnetic field. The lowest energy values and the equilibrium internuclear distances of 1πsub(g) state are also calculated for various magnetic field. (author)

  16. Statistical investigation of surface bound ions and further development of BION server to include pH and salt dependence.

    Science.gov (United States)

    Petukh, Marharyta; Zhang, Min; Alexov, Emil

    2015-12-15

    Ions are engaged in multiple biological processes in cells. By binding to the macromolecules or being mobile in the solvent, they maintain the integrity of the structure of macromolecules; participate in their enzymatic activity; or screen electrostatic interactions. While experimental methods are not always able to assign the exact location of ions, computational methods are in demand. Although the majority of computational methods are successful in predicting the position of ions buried inside macromolecules, they are less effective in deciphering positions of surface bound ions. Here, we propose the new BION algorithm (http://compbio.clemson.edu/bion_server_ph/) that predicts the location of the surface bound ions. It is more efficient and accurate compared to the previous version since it uses more advanced clustering algorithm in combination with pairing rules. In addition, the BION webserver allows specifying the pH and the salt concentration in predicting ions positions. © 2015 Wiley Periodicals, Inc.

  17. AES, EELS and TRIM simulation method study of InP(100 subjected to Ar+, He+ and H+ ions bombardment.

    Directory of Open Access Journals (Sweden)

    Abidri B.

    2012-06-01

    Full Text Available Auger Electron Spectroscopy (AES and Electron Energy Loss Spectroscopy (EELS have been performed in order to investigate the InP(100 surface subjected to ions bombardment. The InP(100 surface is always contaminated by carbon and oxygen revealed by C-KLL and O-KLL AES spectra recorded just after introduction of the sample in the UHV spectrometer chamber. The usually cleaning process of the surface is the bombardment by argon ions. However, even at low energy of ions beam (300 eV indium clusters and phosphorus vacancies are usually formed on the surface. The aim of our study is to compare the behaviour of the surface when submitted to He+ or H+ ions bombardment. The helium ions accelerated at 500V voltage and for 45 mn allow removing contaminants but induces damaged and no stoichiometric surface. The proton ions were accelerated at low energy of 500 eV to bombard the InP surface at room temperature. The proton ions broke the In-P chemical bonds to induce the formation of In metal islands. Such a chemical reactivity between hydrogen and phosphorus led to form chemical species such as PH and PH3, which desorbed from the surface. The chemical susceptibly and the small size of H+ advantaged their diffusion into bulk. Since the experimental methods alone were not able to give us with accuracy the disturbed depth of the target by these ions. We associate to the AES and EELS spectroscopies, the TRIM (Transport and Range of Ions in Matter simulation method in order to show the mechanism of interaction between Ar+, He+ or H+ ions and InP and determine the disturbed depth of the target by argon, helium or proton ions.

  18. Amylase for Apple Juice Processing: Effects of pH, Heat, and Ca2+ Ions

    Directory of Open Access Journals (Sweden)

    Liliana N. Ceci

    2002-01-01

    Full Text Available The aim of this paper was to evaluate the effects of pH, heat, and Ca2+ ions on the α-amylase activities in a commercial amylolytic enzyme (Tyazyme L300, used for apple juice processing. Kinetics of thermal inactivation was studied in acetate and citrate/phosphate buffers at different temperatures (55–70 °C and enzyme concentrations (0.276 and 0.552 mL/100 mL. Maximum α-amylase activity was observed at pH=3.4 in both buffers. Effects of the addition of calcium chloride during and after thermal treatments were also investigated. α-amylase activities were measured by an iodometric method and thermal inactivation constants and D values (time for reducing 90 % of the enzymatic activity were estimated. The enzyme was more sensible to pH changes and heat when citrate ions were present in the reaction medium. If Ca2+ in the enzyme structure is bound to citrate then the resistance of the enzyme to pH changes and heat is lowered. Kinetics obtained according to Arrhenius equation and two enzymatic fractions (thermo-labile and thermoresistant were observed too. In citrate buffer the following relation was observed for thermo-labile fraction: log (D value = -0.144 t/°C + 12.992. The level of thermal inactivation also depended on the enzyme concentration. Higher thermal inactivation rates were obtained by increasing the enzyme concentration in the case when citrate was present. It was also found that the addition of calcium chloride (1 g/L after thermal treatment in median containing citrate reactivated the enzyme treated at 60 and 65 °C. The possible implications of these findings in apple juice processing were discussed.

  19. The diffusion of ion implanted hydrogen in amorphous Si3N4:H films

    Science.gov (United States)

    Schmidt, H.; Gruber, W.; Borchardt, G.; Bruns, M.; Rudolphi, M.; Baumann, H.

    2004-06-01

    The tracer diffusion of hydrogen is studied in amorphous Si3N4:H films which were produced by rf magnetron reactive sputtering. The diffusion experiments were carried out in the temperature range between 700 and 1000 °C with ion implanted deuterium isotopes. Secondary ion mass spectrometry was used for depth profile analysis. While a considerable part of the tracer is immobilized due to the interaction with the implantation damage, the other part migrates freely into the film, wherefrom diffusivities are extracted. These diffusivities coincide with those obtained from a control experiment with a gas exchange technique, demonstrating that the implantation damage has no significant influence on the determination of the correct diffusivities themselves.2H transport can be described by the concept of trap limited diffusion, where the tracer atoms are temporarily trapped by intrinsic film defects, presumably nitrogen dangling bonds. For the present case of a considerably high dissociation rate of trapped hydrogen, effective diffusivities are derived which obey an Arrhenius behaviour with a large activation energy of DgrE = 3.4 eV and a pre-exponential factor of D0 = 5 × 10-4 m2 s-1. The effect on diffusion of pre-annealing the films prior to diffusion in nitrogen and possible structural rearrangements involved, as well as of charging the films with hydrogen up to 2.6 at.%, is analysed.

  20. Measurement of Individual H+ and O+ Ion Temperatures in the Topside Ionosphere

    Science.gov (United States)

    Hsu, Chih-Te; Heelis, Roderick A.

    2018-02-01

    Plasma temperatures in the ionosphere are associated with both the dynamics and spatial distribution of the neutral and charge particles. During the daytime, temperatures are determined by solar energy inputs and energy exchange between charged and neutral particles. Plasma transport parallel to the magnetic field adds another influence on temperatures through adiabatic processes that are most evident during the nighttime. Previous observations suggest that the topside H+ temperature (TH+) should reside between the O+ temperature (TO+) and the electron temperature (Te), and further calculations confirm the preferential heat transfer from the electrons to H+ in the topside. In this work we implement a more sophisticated analysis procedure to extract individual mass-dependent ion temperatures from the retarding potential analyzer measurements on the DMSP F15 satellite. The results show that the daytime TH+ is a few hundred degrees higher than TO+ at all longitudes. The nighttime temperature difference between TH+ and TO+ is indicative of mass-dependent adiabatic heating and cooling processes across the equatorial region. The ion temperatures and measured plasma flows present clear longitudinal variations that are associated with magnetic declination.

  1. Evaluation of calcium ion, hydroxyl ion release and pH levels in various calcium hydroxide based intracanal medicaments: An in vitro study.

    Science.gov (United States)

    Fulzele, Punit; Baliga, Sudhindra; Thosar, Nilima; Pradhan, Debaprya

    2011-10-01

    Evaluation of calcium ion and hydroxyl ion release and pH levels in various calcium hydroxide based intracanal medicaments. The purpose of this study was to evaluate calcium and hydroxyl ion release and pH levels of calcium hydroxide based products, namely, RC Cal, Metapex, calcium hydroxide with distilled water, along with the new gutta-percha points with calcium hydroxide. The materials were inserted in polyethylene tubes and immersed in deionized water. The pH variation, Ca(++) and OH(-) release were monitored periodically for 1 week. Statistical analysis was carried out using one-way analysis of variance and Tukey's post hoc tests with PASW Statistics version 18 software to compare the statistical difference. After 1 week, calcium hydroxide with distilled water and RC Cal raised the pH to 12.7 and 11.8, respectively, while a small change was observed for Metapex, calcium hydroxide gutta-percha points. The calcium released after 1 week was 15.36 mg/dL from RC Cal, followed by 13.04, 1.296, 3.064 mg/dL from calcium hydroxide with sterile water, Metapex and calcium hydroxide gutta-percha points, respectively. Calcium hydroxide with sterile water and RC Cal pastes liberate significantly more calcium and hydroxyl ions and raise the pH higher than Metapex and calcium hydroxidegutta-percha points.

  2. Orientation and impact-parameter dependence of dissociative ionization of H{sub 2} by slow ion impact

    Energy Technology Data Exchange (ETDEWEB)

    Afaneh, F [Physics Department, Hashemite University, PO Box 150459, Zarqa 13115 (Jordan); Schmidt, L Ph H [Institut fuer Kernphysik, Max-von-Laue-Str. 1, 60438 Frankfurt (Germany); Schoeffler, M [Institut fuer Kernphysik, Max-von-Laue-Str. 1, 60438 Frankfurt (Germany); Stiebing, K E [Institut fuer Kernphysik, Max-von-Laue-Str. 1, 60438 Frankfurt am Main (Germany); Al-Jundi, J [Physics Department, Hashemite University, PO Box 150459, Zarqa 13115 (Jordan); Schmidt-Boecking, H [Institut fuer Kernphysik, Max-von-Laue-Str. 1, 60438 Frankfurt (Germany); Doerner, R [Institut fuer Kernphysik, Max-von-Laue-Str. 1, 60438 Frankfurt (Germany)

    2007-09-14

    We have used the cold target recoil ion momentum spectroscopy imaging technique to investigate dissociative ionization of H{sub 2} by 25 keV proton impact. A kinematically complete picture of the dissociative ionization dynamics for slow proton collision has been obtained. The results show a strong impact-parameter dependence of the fragmentation process of H{sub 2}. This clearly emerged in the energy distributions of the H{sup +} ions generated for different impact parameters. At large impact parameters the H{sup +} ions equally share the energy liberated in the collision whereas at small impact parameters, the energy sharing is quite asymmetric. We also observed a strong dependence of the electron emission on molecular alignment. The momentum distribution of the emitted electron generated for a fixed-in-space H{sub 2} molecule displays that the electrons are more likely to be emitted perpendicular to the molecular axis.

  3. Corrosion inhibition of iron in 0.5 mol L-1 H2SO4 by halide ions

    Directory of Open Access Journals (Sweden)

    Jeyaprabha C.

    2006-01-01

    Full Text Available The inhibition effect of halide ions such as iodide, bromide and chloride ions on the corrosion of iron in 0.5 mol L-1 H2SO4 and the adsorption behaviour of these ions on the electrode surface have been studied by polarization and impedance methods. It has been found that the inhibition of nearly 90% has been observed for iodide ions at 2.5 10-3 mol L-1, for bromide ions at 10 10-3 mol L-1 and 80% for chloride ions at 2.5 10-3 mol L-1. The inhibition effect is increased with increase of halide ions concentration in the case of I- and Br- ions, whereas it has decreased in the case of Cl- ion at concentrations higher than 5 10-3 mol L-1. The double layer capacitance values have decreased considerably in the presence of halide ions which indicate that these anions are adsorbed on iron at the corrosion potential.

  4. Study of the ionization of H{sup +}{sub 2} ions in strong laser fields; Untersuchung der Ionisation von H{sup +}{sub 2}-Ionen in starken Laserfeldern

    Energy Technology Data Exchange (ETDEWEB)

    Odenweller, Matthias

    2010-07-01

    In the framework of this thesis it has been succeeded to develop a worldwide unique measurement apparatur, by which hydrogen-molecule ions can be ionized by means of short laser pulses and the reaction product kinematically completely measured. For this a detection method following the Coltrims technique, in which both protons and electrons can be detected over the complete spatial angle. The H{sup +}{sub 2} ions origin from a high-frequency ion source and are accelerated to 400 keV. This ion beam is overlapped with a 780-nm laser pulse othe pulse length 40 fs. After the reaction the molecule ions fragments either via the dissociation channel H{sup +}{sub 2}+nh{nu}{yields}H+H{sup +} or via an ionization followed by a Coulomb explosion: H{sup +}{sub 2}+nh{nu}{yields}H{sup +}+H{sup +}+e{sup -}. The projectiles are detected after a drift path of about 3 m on an ion detector. For the detection of the electrons a special spectrometer was concipated. In the reaction it comes by the comparatively long pulse length already at low intensities to dissociation processes. The dissociating molecule reaches still during the increasing side of the laser pulse in this way distances, in which the charge-resonance-enhanced-ionization (CREI) can take place. Also the angular distribution of the measured protons lying in a very small angular range around the polarization direction of the laser suggests that CREI is the dominant ionization process. At circular polarization however a netto-acceleration of the electrons perpendicularly to the direction of the electric field at the ionization time takes place, so that the measurement of the electron momenta represents a suited measurement quantity for the study of the ionization process. By this way angular distributions of the electrons relatively to the internuclear axis within the polarization plane could be measured.

  5. CW/Pulsed H{sup −} ion beam generation with PKU Cs-free 2.45 GHz microwave driven ion source

    Energy Technology Data Exchange (ETDEWEB)

    Peng, S. X., E-mail: sxpeng@pku.edu.cn; Ren, H. T.; Xu, Y.; Zhang, T.; Zhang, J. F.; Zhao, J.; Guo, Z. Y. [State Key Laboratory of Nuclear Physics and Technology and Institute of Heavy Ion Physics, School of Physics, Peking University, Beijing 100871, People' s Republic of China (China); Zhang, A. L. [University of Chinese Academy of Sciences, Beijing 100049, People' s Republic of China (China); Chen, J. E. [State Key Laboratory of Nuclear Physics and Technology and Institute of Heavy Ion Physics, School of Physics, Peking University, Beijing 100871, People' s Republic of China (China); University of Chinese Academy of Sciences, Beijing 100049, People' s Republic of China (China)

    2015-04-08

    Circular accelerators used for positron emission tomography (PET, i.e. accelerator used for make radio isotopes) need several mA of CW H- ion beam for their routine operation. Other facilities, like Space Radio-Environment Simulate Assembly (SPRESA), require less than 10 mA pulsed mode H{sup −} beam. Caesium free negative hydrogen ion source is a good choice for those facilities because of its compact structure, easy operation and low cost. Up to now, there is no H{sup −} source able to produce very intense H{sup −} beams with important variation of the duty factor{sup [1]}. Recently, a new version of 2.45 GHz microwave H{sup −} ion source was designed at PKU, based on lessons learnt from the previous one. This non cesiated source is very compact thanks to its permanent magnet configuration. Special attention was paid on the design of the discharge chamber structure, electron dumping and extraction system. Source test to produce H{sup −} ion beams in pulsed and CW mode was carried out on PKU ion source test bench. In CW mode, a 10.8 mA/30keV H{sup −} beam with rms emittance about 0.16 π·mm·mrad has been obtained with only 500 W rf power. The power efficiency reaches 21 mA/kW. In pulsed mode with duty factor of 10% (100Hz/1ms), this compact source can easily deliver 20 mA H{sup −} ion beam at 35 keV with rms emittance about 0.2 π·mm·mrad when RF power is set at 2.2 kW (peak power). Several hour successive running operation in both modes and totaling more than 200 hours proves its high quality. The outside dimension of this new H{sup −} source body is ϕ116 mm × 124 mm, and the entire H{sup −} source infrastructure, including rf matching section, plasma chamber and extraction system, is ϕ310 × 180 mm. The high voltage region is limited with in a ϕ310 mm × 230 mm diagram. Details are given in this paper.

  6. Evaluation of pH, calcium ion release and antimicrobial activity of a new calcium aluminate cement

    Directory of Open Access Journals (Sweden)

    Fernanda de Carvalho Panzeri Pires-de-Souza

    2013-07-01

    Full Text Available This study evaluated the pH, calcium ion release and antimicrobial activity of EndoBinder (EB, containing different radiopacifiers: bismuth oxide (Bi2O3, zinc oxide (ZnO or zirconium oxide (ZrO2, in comparison to MTA. For pH and calcium ion release tests, 5 specimens per group (n = 5 were immersed into 10 mL of distilled and deionized water at 37°C. After 2, 4, 12, 24, 48 h; 7, 14 and 28 days, the pH was measured and calcium ion release quantified in an atomic absorption spectrophotometer. For antimicrobial activity, the cements were tested against S. aureus, E. coli, E. faecalis and C. albicans, in triplicate. MTA presented higher values for pH and calcium ion release than the other groups, however, with no statistically significant difference after 28 days (p > 0.05; and the largest inhibition halos for all strains, with no significant difference (E. coli and E. faecalis for pure EB and EB + Bi2O3 (p > 0.05. EB presented similar performance to that of MTA as regards pH and calcium ion release; however, when ZnO and ZrO2 were used, EB did not present antimicrobial activity against some strains.

  7. Multiresponsive polysiloxane bearing spiropyran: synthesis and sensing of pH and metal ions of different valence

    Science.gov (United States)

    Li, Hongqi; Zheng, Tao; Zhao, Yong; Xu, Zhenxiang; Dai, Xuhang; Shao, Zhiyu

    2018-03-01

    A spiropyran-appended polysiloxane (SP-Si) was synthesized and characterized. The pH-responsive behavior of SP-Si was investigated. It was found that with the decrease of the pH of SP-Si solution the intensity of the absorption peak at 440 nm increased and the color of SP-Si solution turned from colorless to yellow gradually. The polymer serves as chemosensor for colorimetric detection of Ag+ and Fe3+ ions. Addition of Ag+ and Fe3+ ions to SP-Si solution induced color change from colorless to brown and earthy yellow, respectively. Sensing of Ag+ ions by SP-Si was not affected by common competitive metal ions except Hg2+ ions. Based on the transformation from colorless SP-Si solution with negligible absorption at 440 nm to brown SP-Si/Ag+ showing extremely strong absorption at 440 nm by addition of Ag+ ions and subsequent transformation from brown to colorless SP-Si/Ag+/Hg2+ with relatively weak absorption at 440 nm after addition of 1 equivalent of Hg2+ ions, SP-Si/Ag+ system serves as a dual colorimetric and spectroscopic probe for highly selective and sensitive detection of Hg2+ ions. The selective detection of Fe3+ ions by SP-Si is not interfered by common competitive metal ions including Na+, K+, Li+, Hg2+, Ni2+, Fe2+, Zn2+, Co2+, Sr2+, Cu2+, Al3+, Ce3+ and Cr3+. The detection limit of Ag+ and Fe3+ ions is 1.45 × 10‑6 M and 3.52 × 10‑6 M, respectively.

  8. pH-gradient ion-exchange chromatography: An analytical tool for design and optimization of protein separations

    NARCIS (Netherlands)

    Ahamed, T.; Nfor, B.; Verhaert, P.; Deden, van G.; Wielen, van der L.

    2007-01-01

    This work demonstrates that a highly linear, controllable and wide-ranged pH-gradient can be generated through an ion-exchange chromatography (IEC) column. Such a pH-gradient anion-exchange chromatography was evaluated with 17 model proteins and found that acidic (pI <6) and basic (pI > 8)

  9. ADSORPSI ION CU(II MENGGUNAKAN PASIR LAUT TERAKTIVASI H2SO4 DAN TERSALUT Fe2O3

    Directory of Open Access Journals (Sweden)

    DS Pambudi

    2014-11-01

    Full Text Available Pasir laut merupakan bahan alam yang melimpah. Selain digunakan sebagai bahan bangunan, pasir dapat dimanfaatkan sebagai penjerap ion logam berat mengingat 30% lebih dari volumenya adalah pori-pori. Tujuan penelitian adalah untuk mengetahui kapasitas adsorpsi ion logam Cu(II menggunakan pasir laut kontrol, pasir laut teraktivasi H2SO4, pasir laut tersalut Fe2O3, serta pasir laut teraktivasi H2SO4 dan tersalut Fe2O3. Ada dua macam pasir laut yang digunakan, yaitu pasir hitam dan pasir putih. Kajian yang dilakukan meliputi optimasi adsorben pada variasi pH, konsentrasi ion logam, dan waktu kontak. Optimasi pH diperoleh pada pH 7, optimasi konsentasi ion logam diperoleh 250 ppm untuk pasir hitam dan 200 ppm untuk pasir putih, dan optimasi waktu diperoleh 60 menit untuk pasir hitam dan 90 menit untuk pasir putih. Kapasitas adsorpsi pasir laut teraktivasi H2SO4 dan tersalut Fe2O3 dalam menyerap ion logam tembaga sebesar 24,8634 mg/g untuk pasir hitam dan 19,8854 mg/g untuk pasir putih. Sebanyak 6,5 g pasir hitam teraktivasi H2SO4 dan tersalut Fe2O3 digunakan untuk menyerap limbah pada konsentrasi Cu(II sebesar 2960,32 ppm dengan persentase teradsorpsi sebesar 94,70%. Sedangkan pada pasir putih teraktivasi H2SO4 dan tersalut Fe2O3, sebanyak 8 g pasir digunakan untuk menyerap limbah dengan konsentrasi Cu(II sebesar 2984,13 ppm, hasilnya menunjukkan 92,56% ion logam Cu(II teradsorp. Sea sand is abundant natural materials. In addition to be used as a building material, sand can be utilized as heavy metal ion adsorbent, because it has quite a lot of pores, i.e 30% more than its volume. The purpose of this study was to determine the adsorption capacity of Cu(II ions using sea sand alone as control, H2SO4-activated sea sand, Fe2O3-coated sea sand, as well as H2SO4-activated and Fe2O3-coated sea sand. Two kinds of sea sand have been used in the research, i.e the black sand and the white sand. Studies were performed to examine the optimization of the

  10. MHD-induced Energetic Ion Loss during H-mode Discharges in the National Spherical Torus Experiment (NSTX)

    Energy Technology Data Exchange (ETDEWEB)

    S.S. Medley; N.N. Gorelenkov; R. Andre; R.E. Bell; D.S. Darrow; E.D. Fredrickson; S.M. Kaye; B.P. LeBlanc; A.L. Roquemore; and the NSTX Team

    2004-03-15

    MHD-induced energetic ion loss in neutral-beam-heated H-mode [high-confinement mode] discharges in NSTX [National Spherical Torus Experiment] is discussed. A rich variety of energetic ion behavior resulting from magnetohydrodynamic (MHD) activity is observed in the NSTX using a horizontally scanning Neutral Particle Analyzer (NPA) whose sightline views across the three co-injected neutral beams. For example, onset of an n = 2 mode leads to relatively slow decay of the energetic ion population (E {approx} 10-100 keV) and consequently the neutron yield. The effect of reconnection events, sawteeth, and bounce fishbones differs from that observed for low-n, low-frequency, tearing-type MHD modes. In this case, prompt loss of the energetic ion population occurs on a time scale of less than or equal to 1 ms and a precipitous drop in the neutron yield occurs. This paper focuses on MHD-induced ion loss during H-mode operation in NSTX. After H-mode onset, the NPA charge-exchange spectrum usually exhibits a significant loss of energetic ions only for E > E(sub)b/2 where E(sub)b is the beam injection energy. The magnitude of the energetic ion loss was observed to decrease with increasing tangency radius, R(sub)tan, of the NPA sightline, increasing toroidal field, B(sub)T, and increasing neutral-beam injection energy, E(sub)b. TRANSP modeling suggests that MHD-induced ion loss is enhanced during H-mode operation due to an evolution of the q and beam deposition profiles that feeds both passing and trapped ions into the region of low-n MHD activity. ORBIT code analysis of particle interaction with a model magnetic perturbation supported the energy selectivity of the MHD-induced loss observed in the NPA measurements. Transport analysis with the TRANSP code using a fast-ion diffusion tool to emulate the observed MHD-induced energetic ion loss showed significant modifications of the neutral- beam heating as well as the power balance, thermal diffusivities, energy confinement times

  11. pH-Dependent metal ion toxicity influences the antibacterial activity of two natural mineral mixtures.

    Directory of Open Access Journals (Sweden)

    Tanya M Cunningham

    2010-03-01

    Full Text Available Recent studies have demonstrated that several mineral products sold for medicinal purposes demonstrate antimicrobial activity, but little is known about the physicochemical properties involved in antibacterial activity.Using in vitro mineral suspension testing, we have identified two natural mineral mixtures, arbitrarily designated BY07 and CB07, with antibacterial activity against a broad-spectrum of bacterial pathogens. Mineral-derived aqueous leachates also exhibited antibacterial activity, revealing that chemical, not physical, mineral characteristics were responsible for the observed activity. The chemical properties essential for bactericidal activity against Escherichia coli were probed by testing antibacterial activity in the presence of metal chelators, the hydroxyl radical scavenger, thiourea, and varying pH levels. Chelation of the BY07 minerals with EDTA or desferrioxamine eliminated or reduced BY07 toxicity, respectively, suggesting a role of an acid-soluble metal species, particularly Fe(3+ or other sequestered metal cations, in mineral toxicity. This conclusion was supported by NMR relaxation data, which indicated that BY07 and CB07 leachates contained higher concentrations of chemically accessible metal ions than leachates from non-bactericidal mineral samples.We conclude that the acidic environment of the hydrated minerals significantly contributes to antibacterial activity by increasing the availability and toxicity of metal ions. These findings provide impetus for further investigation of the physiological effects of mineral products and their applications in complementary antibacterial therapies.

  12. Failure Mechanisms of Ni-H2 and Li-Ion Batteries Under Hypervelocity Impacts

    Science.gov (United States)

    Miller, J. E.; Lyons, F.; Christiansen, E. L.; Lear, D. M.

    2017-01-01

    Lithium-Ion (Li-Ion) batteries have yielded significant performance advantages for many industries, including the aerospace industry, and have been selected to replace nickel hydrogen (Ni-H2) batteries for the International Space Station (ISS) program to meet the energy storage demands. As the ISS uses its vast solar arrays to generate its power, the solar arrays meet their sunlit power demands and supply excess power to battery packs for power delivery on the sun obscured phase of the approximate 90 minute low Earth orbit. These large battery packs are located on the exterior of the ISS, and as such, the battery packs are exposed to external environment threats like naturally occurring meteoroids and artificial orbital debris (MMOD). While the risks from these solid particle environments has been known and addressed to an acceptable risk of failure through shield design, it is not possible to completely eliminate the risk of loss of these assets on orbit due to MMOD, and as such, failure consequences to the ISS have been considered.

  13. H-isotope retention and thermal/ion-induced release in boronized films

    International Nuclear Information System (INIS)

    Walsh, D.S.; Doyle, B.L.; Wampler, W.R.; Hays, A.K.

    1990-01-01

    Over the past decade, it has been clearly demonstrated that the composition of the very near surface (∼100nm) of plasma-interactive components plays a determinant role in most processes which occur in the plasma-edge of Tokamaks. Two very successful techniques to effect control of the plasma-wall interaction are (1) in-situ deposition of amorphous carbon or boron-carbon films and (2) the use of He/C conditioning discharges or He glow discharge cleaning to modify the near surface of bulk graphite components. We have deposited boronized layers into Si using plasma-assisted CVD and sputter deposition. The PCVD deposition conditions were as close as possible to those used in TFTR, and some films deposited in TFTR have also been studied. Using these two deposition techniques, B x CH y films have been produced with x varying from 1/2 -- 4, and y from ∼1 (sputtered) to ∼3 (PCVD). Most films also contained significant amounts of 0. Thermal and ion-induced release of H-isotopes from BC films is qualitatively similar to that measured for graphite. Implanted H saturates in these films at a H/host atom ratio of 0.7 which is considerably higher than that of graphite(∼0.4). As-deposited PCVD films are already saturated with H, while sputtered films are not. Sputtered BC films therefore possess an inherent H-pumping capability which could prove to be extremely beneficial to TFTR. 16 refs., 5 figs., 1 tab

  14. Influence of the ion nitriding temperature in the wear resistance of AISI H13 tool steel

    International Nuclear Information System (INIS)

    Heck, Stenio Cristaldo; Fernandes, Frederico Augusto Pires; Pereira, Ricardo Gomes; Casteletti, Luiz Carlos; Totten, George Edward

    2010-01-01

    The AISI H13 tool steel for hot work is the most used in its category. This steel was developed for injection molds and extrusion of hot metals as well as for conformation in hot presses and hammers. Plasma nitriding can improve significantly the surface properties of these steels, but the treatments conditions, such as temperature, must be optimized. In this work the influence of nitriding treatment temperature on the wear behavior of this steel is investigated. Samples of AISI H13 steel were quenched and tempered and then ion nitrided in the temperatures of 450, 550 and 650 deg C, at 4mbar pressure, during 5 hours. Samples of the treated material were characterized by optical microscopy, Vickers microhardness, x-ray analysis and wear tests. Plasma nitriding formed hard diffusion zones in all the treated samples. White layers were formed in samples treated at 550 deg C and 650 deg C. The treatment temperature of 450 deg C produced the highest hardness. Treatment temperature showed great influence in the diffusion layer thickness. X-ray analysis indicated the formation of the Fe 3 N, Fe 4 N and CrN phases for all temperatures, but with different concentrations. Nitriding increased significantly the AISI H13 wear resistance. (author)

  15. Abrupt onset of large scale nonproton ion release in purple membranes caused by increasing pH or ionic strength.

    Science.gov (United States)

    Marinetti, T

    1987-06-01

    The abrupt onset of large scale nonproton ion release by photo-excited purple membrane suspensions has been observed near neutral pH using transient conductivity measurements. At pH 7 and low ionic strength, the conductivity transients due to proton and nonproton ions are of comparable magnitude but of opposite sign: fast proton release and ion uptake, followed by slow proton uptake and ion release. By increasing either the pH or the NaCl concentration, the amplitude of the conductivity transient increases sharply and the signal is then dominated by nonproton ion release. These results can be understood in terms of light-induced changes in the population of counterions condensed at the purple membrane surface caused by changes in the surface charge density. The critical charge density required for condensation to occur is evidently achieved near neutral pH by ionizing dissociable groups on the membrane by either titration (increasing the pH) or shifting their pKs (increasing the ionic strength).

  16. Effects of electric fields on the photodetachment cross section of the H- ion near threshold

    International Nuclear Information System (INIS)

    Stewart, J.E.

    1987-12-01

    The photodetachment cross section of the H - ion near the one electron threshold in electric fields ranging from approximately 5 x 10 -7 atomic units up to 2.4 x 10 -4 atomic units has been studied using an 800 MeV beam at the Los Alamos National Laboratory. The lowest field data, analyzed as though at zero field, are consistent with the Wigner prediction for p wave processes. At greater field values, photodetachment using σ polarized laser light displays the expected lowering of apparent threshold and evidence of tunneling. Using π polarized laser light the same features are seen with the addition of oscillations superimposed on the cross section. Three complementary explanations are presented for the oscillations. 42 refs., 35 figs., 8 tabs

  17. Laser diagnostics of H- formation in a magnetic multicusp ion source

    International Nuclear Information System (INIS)

    Young, A.T.; Chen, P.; Kunkel, W.B.; Leung, K.N.; Li, C.Y.; Stutzin, G.C.

    1991-05-01

    The populations of ground electronic state atomic hydrogen and ground electronic state, vibrationally-rotationally excited hydrogen molecules in a negative hydrogen ion source discharge have been measured using vacuum ultraviolet (VUV) laser absorption spectroscopy. Vibrational states up to v=8 and rotational levels as high as J=15 have been measured. The measurements have been made under a range of discharge conditions. The complete vibrational population distribution for v=1-8, J=1 has been obtained. The vibrational distribution appears to be thermalized and does not exhibit a ''plateau'' at the higher vibrational levels, in contrast to most models of this system. In contrast, the high rotational states are populated suprathermally. These determinations indicate that rotationally excited molecules may play an important role in the production of H minus in these sources. 5 refs., 5 figs

  18. Modelling the distribution of a(w), pH and ions in marinated beef meat.

    Science.gov (United States)

    Lebert, André; Daudin, Jean-Dominique

    2014-07-01

    New beef products from low value cuts could be developed using marinating since this process has been shown to improve meat sensorial properties and shelf life. However, to optimise the process mathematical models are needed to predict evolution of the physicochemical properties that determine biochemical and structural changes. Two major works have been carried out to elaborate comprehensive models: (1) Thermodynamic models were adapted to predict water sorption isotherms and pH of beef meat tissue in presence of salts (NaCl, KCl) and organic acids (acetic, lactic, citric and ascorbic acid), (2) Fickian numerical models were set up to predict the migration of ions within meat cuts using apparent diffusivities previously estimated from 1D experiments. Simulation calculations showed reasonable agreement with measurements and can be used to investigate the effect of marinating conditions, product heterogeneity, dimension and shape. © 2013 Elsevier Ltd. All rights reserved.

  19. Rotational Laser Cooling of MgH+ Ions and Rotational Rate Measurements

    DEFF Research Database (Denmark)

    Hansen, Anders Kragh; Staanum, Peter; Højbjerre, Klaus

    A method of laser cooling vibrationally and translationally cold trapped MgH+ ions to the rotational ground state using optical pumping was recently demonstrated in our group [1]. This method relies on the 293 K blackbody radiation to redistribute population among the rotational states, while...... exciting a single rovibrational transition within the X1Σ+ electronic ground state for optical pumping into the rovibrational ground state. To model the expected rotational state distributions after the application of the laser beam, one has to know the various rotational transitions rates in the present...... blackbody radiation field. To undertake such modelling, we will carry out measurements of a series of transition rates between rotational states in the vibronic ground state at room temperature. The measurements will be performed by the same Resonance Enhanced Multi-Photon Dissociation (REMPD) process used...

  20. Equilibria model for pH variations and ion adsorption in capacitive deionization electrodes.

    Science.gov (United States)

    Hemmatifar, Ali; Oyarzun, Diego I; Palko, James W; Hawks, Steven A; Stadermann, Michael; Santiago, Juan G

    2017-10-01

    Ion adsorption and equilibrium between electrolyte and microstructure of porous electrodes are at the heart of capacitive deionization (CDI) research. Surface functional groups are among the factors which fundamentally affect adsorption characteristics of the material and hence CDI system performance in general. Current CDI-based models for surface charge are mainly based on a fixed (constant) charge density, and do not treat acid-base equilibria of electrode microstructure including so-called micropores. We here expand current models by coupling the modified Donnan (mD) model with weak electrolyte acid-base equilibria theory. In our model, surface charge density can vary based on equilibrium constants (pK's) of individual surface groups as well as micropore and electrolyte pH environments. In this initial paper, we consider this equilibrium in the absence of Faradaic reactions. The model shows the preferential adsorption of cations versus anions to surfaces with respectively acidic or basic surface functional groups. We introduce a new parameter we term "chemical charge efficiency" to quantify efficiency of salt removal due to surface functional groups. We validate our model using well controlled titration experiments for an activated carbon cloth (ACC), and quantify initial and final pH of solution after adding the ACC sample. We also leverage inductively coupled plasma mass spectrometry (ICP-MS) and ion chromatography (IC) to quantify the final background concentrations of individual ionic species. Our results show a very good agreement between experiments and model. The model is extendable to a wide variety of porous electrode systems and CDI systems with applied potential. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Experimental study of high current negative ion sources D{sup -} / H{sup -}. Analysis based on the simulation of the negative ion transport in the plasma source; Etude experimentale de sources a fort courant d`ions negatifs D{sup -} / H{sup -}. Analyse fondee sur la simulation du transport des ions dans le plasma de la source

    Energy Technology Data Exchange (ETDEWEB)

    Riz, D.

    1996-10-30

    In the frame of the development of a neutral beam injection system able to work the ITER tokamak (International Thermonuclear Experimental Reactor), two negative ion sources, Dragon and Kamaboko, have been installed on the MANTIS test bed in Cadarache, and studies in order to extract 20 mA/cm{sup 2} of D{sup -}. The two production modes of negative ions have been investigated: volume production; surface production after cesium injection in the discharge. Experiments have shown that cesium seeding is necessary in order to reach the requested performances for ITER. 20 mA/cm{sup 2} have been extracted from the Kamaboko source for an arc power density of 2.5 kW/liter. Simultaneously, a code called NIETZSCHE has been developed to simulate the negative ions transport in the source plasma, from their birth place to the extraction holes. The ion trajectory is calculated by numerically solving the 3D motion equation, while the atomic processes of destruction, of elastic collisions H{sup -}/H{sup +} and of charge exchange H{sup -}/H{sup 0} are handled at each time step by a Monte Carlo procedure. The code allows to obtain the extraction probability of a negative ion produced at a given location. The calculations performed with NIETZSCHE have allowed to explain several phenomena observed on negative ion sources, such as the isotopic effect H{sup -}/D{sup -} and the influence of the polarisation of the plasma grid and of the magnetic filter on the negative ions current. The code has also shown that, in the type of sources contemplated for ITER, working with large arc power densities (> 1 kW/liter), only negative ions produced in volume at a distance lower that 2 cm from the plasma grid and those produced at the grid surface have a chance of being extracted. (author). 122 refs.

  2. The ion sensitive field effect transistor (ISFET) pH electrode: a new sensor for long term ambulatory pH monitoring.

    OpenAIRE

    Duroux, P; Emde, C; Bauerfeind, P; Francis, C; Grisel, A; Thybaud, L; Arstrong, D; Depeursinge, C; Blum, A L

    1991-01-01

    Intraluminal pH monitoring in man should be performed with disposable multichannel assemblies that allow recordings at multiple sites and prevent transmission of infection. Currently available glass electrodes are unsuitable for this purpose because of their size and price. We have thus constructed and tested a small, combined ion sensitive field effect transistor (ISFET) pH electrode incorporating an integral reference electrode. In vitro studies showed that both ISFET and glass electrodes (...

  3. Fluorescent derivatives of nucleotides. Metal ion interactions and pH dependency.

    Science.gov (United States)

    Vanderkooi, J M; Weiss, C J; Woodrow, G V

    1979-02-01

    The fluorescence parameters of ethenoadenosine derivatives are influenced by metal cations and pH, as summarized here. The pH profile of ethenoadenosine determined by fluorescence intensity gives a normal titration curve and is not affected by ionic strength. In contrast, the pH titration curves of etheno-ATP, etheno ADP, and etheno AMP depend upon ionic strength. At high ionic strength normal curves are obtained, whereas at low ionic strength anomalies are obtained; this suggests that the phosphates can interact with the ring, possibly by hydrogen binding to the ring nitrogens. The room temperature fluorescence of ethenoadenosine occurs from the base form, although excitation of either the acid or base forms can contribute to the emission. This result can be explained if the excited state pK is lower than the ground state pK, and if deprotonation occurs within the time scale of the excited state. At low pH values the fluorescence lifetime of the base form is dependent upon the buffer concentration, indicating that the reverse reaction, protonation, occurs. The affinity constants for the binding of metals to the ethenoadenosine phosphates resemble those for the corresponding adenosine phosphates. Ni(II) and Co(II) are more effective than Mn(II) in quenching the fluorescence of ethenoadenosine phosphates; this result is predicted by Förster's theory for energy transfer based upon the overlap between donor emission spectrum and acceptor absorption spectrum. The diamagnetic ions Mg(II), Ca(II), and Zn(II) do not appear to affect the fluorescence of the ethenoadenosine phosphates directly, but rather to affect the conformation of the molecule, thereby affecting the quantum yield.

  4. Determination of discharge parameters via OES at the Linac4 H{sup −} ion source

    Energy Technology Data Exchange (ETDEWEB)

    Briefi, S., E-mail: stefan.briefi@physik.uni-augsburg.de [AG Experimentelle Plasmaphysik, Institut für Physik, Universität Augsburg, 86135 Augsburg (Germany); Fink, D.; Mattei, S.; Lettry, J. [Linac4 Ion Source Team, CERN-ABP, 1211 Geneva 23 (Switzerland); Fantz, U. [AG Experimentelle Plasmaphysik, Institut für Physik, Universität Augsburg, 86135 Augsburg (Germany); Max-Planck-Institut für Plasmaphysik, Boltzmannstraße 2, 85748 Garching (Germany)

    2016-02-15

    Optical emission spectroscopy (OES) measurements of the atomic Balmer series and the molecular Fulcher transition have been carried out at the Linac4 ion source in order to determine plasma parameters. As the spectroscopic system was only relatively calibrated, the data evaluation only yielded rough estimates of the plasma parameters (T{sub e} ≈ 1.2 eV, n{sub e} ≈ 1 × 10{sup 19} m{sup −3}, and n{sub H}/n{sub H{sub 2}} ≈ 0.5 at standard operational parameters). The analysis of the Fulcher transition revealed a non-thermal “hockey-stick” rotational population of the hydrogen molecules. At varying RF power, the measurements at the on-axis line of sight (LOS) showed a peak in the rotational temperatures between 25 and 40 kW of RF power, whereas a steady decrease with power was observed at a tilted LOS, indicating the presence of strong plasma parameter gradients.

  5. Producing the positive antihydrogen ion {\\bar{{\\rm{H}}}}^{+} via radiative attachment

    Science.gov (United States)

    Keating, C. M.; Pak, K. Y.; Straton, Jack C.

    2016-04-01

    We provide an estimate of the cross section for the radiative attachment of a second positron into the (1 {{{s}}}2 {}1{{{S}}}e) state of the {\\bar{{{H}}}}+ ion that uses a 200-term two-positron wave function composed of explicitly correlated exponentials. This is done by analytically integrating the six-dimensional, three body photoionization integrals that enter into this result (and those utilizing, the alternative, Hylleraas wave functions) and applying the principle of detailed balance. Finally, we obtain the rate coefficient {α }{RA} for attaching a second positron to antihydrogen as a function of temperature via a numerical integral that is a Maxwell-Boltzmann distribution of the product of positron velocity and cross section. Our motivation in studying the production of {\\bar{{{H}}}}+ lies in its potential use as an intermediate stage in the cooling of antihydrogen to ultra-cold (sub-mK) temperatures for spectroscopic studies and probing the gravitational interaction of the anti-atom. Estimates of the reaction rates are given for positron temperatures T e in the range from 50 K to 5 K.

  6. Decapado de un acero inoxidable austenítico mediante mezclas ecológicas basadas en H2O2 - H2SO4 - iones F-

    Directory of Open Access Journals (Sweden)

    Narváez, L.

    2013-04-01

    Full Text Available This study reports the pickling of 316L stainless steel using mixtures of hydrogen peroxide (H2O2, sulphuric acid (H2SO4 and fluoride ions as hydrofluoric acid (HF, sodium fluoride (NaF and potassium fluoride (KF. The decomposition of H2O2 in the mixtures was assessed at different temperatures 25 °C to 60 °C, with ferric ion contents from 0 to 40 g/l. According to the results obtained, were established the optimal condition pickling at 20 g/l of ferric ions, 25 °C and p-toluensulphonic acid as stabilizer of H2O2. The HF pickling mixture was the only capable to remove totally the oxide layer from the 316L stainless steel after 300 s. The fluoride salts pickling mixtures only remove partially the oxide layer (20 to 40 % aprox. after 300 s. When the pickling time was increased until 1200 s, the removal percentages were around to 80 %.En este estudio se presenta el decapado del acero inoxidable austenítico 316L utilizando mezclas de peróxido de hidrógeno (H2O2/ácido sulfúrico (H2SO4/iones fluoruro; los iones fluoruro provienen del ácido fluorhídrico (HF, fluoruro de sodio (NaF y fluoruro de potasio (KF. La estabilidad del H2O2 fue valorada modificando las concentraciones del ión férrico de 0 a 40 g/l y las temperaturas de 25 °C a 60 °C en las mezclas decapantes. Se establecieron las condiciones óptimas de decapado utilizando 20 g/l de iones férrico a 25 °C empleando el ácido p-toluensulfónico como estabilizante del H2O2. La mezcla que contenía HF fue la única capaz de eliminar completamente los óxidos superficiales del acero a tiempos de 300 s. Las mezclas a base de sales fluoradas eliminaron parcialmente los óxidos (20 y 40 % aprox. en 300 s. Al incrementar el tiempo de decapado hasta 1200 s se obtuvieron porcentajes de eliminación alrededor de un 80 %.

  7. Competitive formation of b(2) and c(2)-H2O ions from b(3) ions containing Asp residue during tandem mass spectrometry: the influence of neighboring Arg.

    Science.gov (United States)

    Guo, Mengzhe; Guo, Cheng; Pan, Yuanjiang

    2014-08-01

    The fragmentation of b3 ions derived from protonated Arg-Xxx-Asp-Ala-Ala (Xxx = Ala, Asp, Glu, Cys) and Arg-Xxx-Glu-Ala-Ala was investigated by electrospray ionization tandem mass spectrometry (MS (n) ) with collision-induced dissociation. A particular ion, which is 1 Da less than b2 ion, is shown to be the c2-H2O ion. The mechanism for its formation involved the aspartic acid in the third position easily losing anhydride to form a c2 ion, which then lost water to form an eight-membered ring of azacyclooctane derivative under the participation of the guanidine of the N-terminal arginine. However, this phenomenon was not observed when the aspartic acid was replaced by glutamic acid. The Amber program was used to determine the conformation of the original c2 residue from the dynamic energy perspective, and then density functional theory-based calculations and changing N-terminal amino acid from arginine to phenylalanine supported this mechanism.

  8. Fragmentation of doubly-protonated peptide ion populations labeled by H/D exchange with CD3OD

    Science.gov (United States)

    Herrmann, Kristin A.; Kuppannan, Krishna; Wysocki, Vicki H.

    2006-03-01

    Doubly-protonated bradykinin (RPPGFSPFR) and an angiotensin III analogue (RVYIFPF) were subjected to hydrogen/deuterium (H/D) exchange with CD3OD in a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer. A bimodal distribution of deuterium incorporation was present for bradykinin after H/D exchange for 90 s at a CD3OD pressure of 4 × 10-7 Torr, indicating the existence of at least two distinct populations. Bradykinin ion populations corresponding to 0-2 and 5-11 deuteriums (i.e., D0, D1, D2, D5, D6, D7, D8, D9, D10, and D11) were each monoisotopically selected and fragmented via sustained off-resonance irradiation (SORI) collision-induced dissociation (CID). The D0-D2 ion populations, which correspond to the slower exchanging population, consistently require lower SORI amplitude to achieve a similar precursor ion survival yield as the faster-reacting (D5-D11) populations. These results demonstrate that conformation/protonation motif has an effect on fragmentation efficiency for bradykinin. Also, the partitioning of the deuterium atoms into fragment ions suggests that the C-terminal arginine residue exchanges more rapidly than the N-terminal arginine. Total deuterium incorporation in the b1/y8 and b2/y7 ion pairs matches very closely the theoretical values for all ion populations studied, indicating that the ions of a complementary pair are likely formed during the same fragmentation event, or that no scrambling occurs upon SORI. Deuterium incorporation into the y1/a8 pseudo-ion pair does not closely match the expected theoretical values. The other peptide, doubly-protonated RVYIFPF, has a trimodal distribution of deuterium incorporation upon H/D exchange with CD3OD at a pressure of 1 × 10-7 Torr for 600 s, indicating at least three distinct ion populations. After 90 s of H/D exchange where at least two distinct populations are detected, the D0-D7 ion populations were monoisotopically selected and fragmented via SORI-CID over a range of SORI

  9. An experimental guided-ion-beam and ab initio study of the ion-molecule gas-phase reactions between Li+ ions and iso-C3H7Cl in their ground electronic state

    International Nuclear Information System (INIS)

    Lucas, J. M.; Andres, J. de; Sogas, J.; Alberti, M.; Aguilar, A.; Bofill, J. M.; Bassi, D.; Ascenzi, D.; Tosi, P.

    2009-01-01

    Reactive collisions between Li + ions and i-C 3 H 7 Cl molecules have been studied in the 0.20-12.00 eV center-of-mass energy range using an octopole radio frequency guided-ion beam apparatus recently developed in our laboratory. At low collision energies, dehydrohalogenation reactions giving rise to Li(C 3 H 6 ) + and Li(HCl) + are the main reaction channels, while at higher ones C 3 H 7 + and C 2 H 3 + become dominant, all their reactive cross sections having been measured as a function of the collision energy. To obtain information about the potential energy surfaces (PESs) on which the reactive processes take place, ab initio calculations at the MP2 level have been performed. For dehydrohalogenations, the reactive ground singlet PES shows ion-molecule adduct formation in both the reactant and product sides of the surface. Following the minimum energy path connecting both minima, an unstable intermediate and the corresponding barriers, both lying below the reactant's energy, have been characterized. The entrance channel ion-molecule adduct is also involved in the formation of C 3 H 7 + , which then generates C 2 H 3 + via an CH 4 unimolecular elimination. A qualitative interpretation of the experimental results based on ab initio calculations is also included.

  10. Cis-[Cr(C2O4(pm(OH22]+ Coordination Ion as a Specific Sensing Ion for H2O2 Detection in HT22 Cells

    Directory of Open Access Journals (Sweden)

    Dagmara Jacewicz

    2014-06-01

    Full Text Available The purpose of this study was to examine the application of the coordinated cis-[Cr(C2O4(pm(OH2]+ cation where pm denotes pyridoxamine, as a specific sensing ion for the detection of hydrogen peroxide (H2O2. The proposed method for H2O2 detection includes two key steps. The first step is based on the nonenzymatic decarboxylation of pyruvate upon reaction with H2O2, while the second step is based on the interaction of cis-[Cr(C2O4(pm(OH22]+ with the CO2 released in the previous step. Using this method H2O2 generated during glutamate-induced oxidative stress was detected in HT22 hippocampal cells. The coordination ion cis-[Cr(C2O4(pm(OH22]+ and the spectrophotometric stopped-flow technique were applied to determine the CO2 concentration in cell lysates, supernatants and cell-free culture medium. Prior to CO2 assessment pyruvate was added to all samples studied. Pyruvate reacts with H2O2 with 1:1 stoichiometry, and consequently the amount of CO2 released in this reaction is equivalent to the amount of H2O2.

  11. ions

    African Journals Online (AJOL)

    (MP2 B2). In order to draw the final conclusion about the content of the isomers of pentaatomic ions in saturated vapor over cesium chloride, we have taken into account the entropy factor. We considered the isomerization reactions which are given below: Cs3Cl2. + (V-shaped) = Cs3Cl2. + (cyclic or bipyramidal). (1). Cs2Cl3.

  12. Recrystallization-Induced Surface Cracks of Carbon Ions Irradiated 6H-SiC after Annealing.

    Science.gov (United States)

    Ye, Chao; Ran, Guang; Zhou, Wei; Shen, Qiang; Feng, Qijie; Lin, Jianxin

    2017-10-25

    Single crystal 6H-SiC wafers with 4° off-axis [0001] orientation were irradiated with carbon ions and then annealed at 900 °C for different time periods. The microstructure and surface morphology of these samples were investigated by grazing incidence X-ray diffraction (GIXRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Ion irradiation induced SiC amorphization, but the surface was smooth and did not have special structures. During the annealing process, the amorphous SiC was recrystallized to form columnar crystals that had a large amount of twin structures. The longer the annealing time was, the greater the amount of recrystallized SiC would be. The recrystallization volume fraction was accorded with the law of the Johnson-Mehl-Avrami equation. The surface morphology consisted of tiny pieces with an average width of approximately 30 nm in the annealed SiC. The volume shrinkage of irradiated SiC layer and the anisotropy of newly born crystals during annealing process produced internal stress and then induced not only a large number of dislocation walls in the non-irradiated layer but also the initiation and propagation of the cracks. The direction of dislocation walls was perpendicular to the growth direction of the columnar crystal. The longer the annealing time was, the larger the length and width of the formed crack would be. A quantitative model of the crack growth was provided to calculate the length and width of the cracks at a given annealing time.

  13. Recrystallization-Induced Surface Cracks of Carbon Ions Irradiated 6H-SiC after Annealing

    Directory of Open Access Journals (Sweden)

    Chao Ye

    2017-10-01

    Full Text Available Single crystal 6H-SiC wafers with 4° off-axis [0001] orientation were irradiated with carbon ions and then annealed at 900 °C for different time periods. The microstructure and surface morphology of these samples were investigated by grazing incidence X-ray diffraction (GIXRD, scanning electron microscopy (SEM, and transmission electron microscopy (TEM. Ion irradiation induced SiC amorphization, but the surface was smooth and did not have special structures. During the annealing process, the amorphous SiC was recrystallized to form columnar crystals that had a large amount of twin structures. The longer the annealing time was, the greater the amount of recrystallized SiC would be. The recrystallization volume fraction was accorded with the law of the Johnson–Mehl–Avrami equation. The surface morphology consisted of tiny pieces with an average width of approximately 30 nm in the annealed SiC. The volume shrinkage of irradiated SiC layer and the anisotropy of newly born crystals during annealing process produced internal stress and then induced not only a large number of dislocation walls in the non-irradiated layer but also the initiation and propagation of the cracks. The direction of dislocation walls was perpendicular to the growth direction of the columnar crystal. The longer the annealing time was, the larger the length and width of the formed crack would be. A quantitative model of the crack growth was provided to calculate the length and width of the cracks at a given annealing time.

  14. Laser induced rovibrational cooling of the linear polyatomic ion C2H2(+).

    Science.gov (United States)

    Deb, Nabanita; Heazlewood, Brianna R; Rennick, Christopher J; Softley, Timothy P

    2014-04-28

    The laser-induced blackbody-assisted rotational cooling of a linear polyatomic ion, C2H2(+), in its (2)Π ground electronic state in the presence of the blackbody radiation field at 300 K and 77 K is investigated theoretically using a rate-equations model. Although pure rotational transitions are forbidden in this non-polar species, the ν5 cis-bending mode is infrared active and the (1-0) band of this mode strongly overlaps the 300 K blackbody spectrum. Hence the lifetimes of state-selected rotational levels are found to be short compared to the typical timescale of ion trapping experiments. The ν5 (1-0) transition is split by the Renner-Teller coupling of vibrational and electronic angular momentum, and by the spin-orbit coupling, into six principal components and these effects are included in the calculations. In this paper, a rotational-cooling scheme is proposed that involves simultaneous pumping of a set of closely spaced Q-branch transitions on the (2)Δ5/2 - (2)Π3/2 band together with two Q-branch lines in the (2)Σ(+) - (2)Π1/2 band. It is shown that this should lead to >70% of total population in the lowest rotational level at 300 K and over 99% at 77 K. In principle, the multiple Q-branch lines could be pumped with just two broad-band (∼Δν = 0.4-3 cm(-1)) infrared lasers.

  15. Effects of water pH and calcium concentration on ion balance in fish of the Rio Negro, Amazon.

    Science.gov (United States)

    Gonzalez, R J; Wood, C M; Wilson, R W; Patrick, M L; Bergman, H L; Narahara, A; Val, A L

    1998-01-01

    We examined the effects of acute low-pH exposure on ion balance (Na+, Cl-, K+) in several species of fish captured from the Rio Negro, a dilute, acidic tributary of the Amazon. At pH 5.5 (untreated Rio Negro water), the four Rio Negro species tested (piranha preta, Serrasalmus rhombeus; piranha branca, Serrasalmus cf. holandi; aracu, Leporinus fasciatus; and pacu, Myleus sp.) were at or near ion balance; upon exposure to pH 3.5, while Na+ and Cl- loss rates became significant, they were relatively mild. In comparison, tambaqui (Colossoma macropomum), which were obtained from aquaculture and held and tested under the same conditions as the other fish, had loss rates seven times higher than all the Rio Negro species. At pH 3.0, rates of Na+ and Cl- loss for the Rio Negro fish increased three- to fivefold but were again much less than those observed in tambaqui. Raising water Ca2+ concentration from 10 micromol L-1 to 100 micromol L-1 during exposure to the same low pH's had no effect on rates of ion loss in the three species tested (piranha preta, piranha branca, aracu), which suggests that either they have such a high branchial affinity for Ca2+ that all sites are saturated at 10 micromol L-1 and additional Ca2+ had no effect, or that Ca2+ may not be involved in regulation of branchial ion permeability. For a final Rio Negro species, the cardinal tetra (Paracheirodon axelrodi), we monitored body Na+ concentration during 5 d of exposure to pH 6.0, 4.0, or 3.5. These pH's had no effect on body Na+ concentration. These data together suggest that exceptional acid tolerance is a general characteristic of fish that inhabit the dilute acidic Rio Negro and raise questions about the role of Ca2+ in regulation of branchial ion permeability in these fish.

  16. Charge Exchange X-Ray Emission due to Highly Charged Ion Collisions with H, He, and H2: Line Ratios for Heliospheric and Interstellar Applications

    Science.gov (United States)

    Cumbee, R. S.; Mullen, P. D.; Lyons, D.; Shelton, R. L.; Fogle, M.; Schultz, D. R.; Stancil, P. C.

    2018-01-01

    The fundamental collisional process of charge exchange (CX) has been established as a primary source of X-ray emission from the heliosphere, planetary exospheres, and supernova remnants. In this process, X-ray emission results from the capture of an electron by a highly charged ion from a neutral atom or molecule, to form a highly excited, high-charge state ion. As the captured electron cascades down to the lowest energy level, photons are emitted, including X-rays. To provide reliable CX-induced X-ray spectral models to realistically simulate these environments, line ratios and spectra are computed using theoretical CX cross sections obtained with the multi-channel Landau-Zener, atomic-orbital close-coupling, molecular-orbital close-coupling, and classical trajectory Monte Carlo methods for various collisional velocities relevant to astrophysics. X-ray spectra were computed for collisions of bare and H-like C to Al ions with H, He, and H2 with results compared to available experimental data. Using these line ratios, XSPEC models of CX emission in the northeast rim of the Cygnus Loop supernova remnant and the heliosphere are shown as examples with ion velocity dependence.

  17. A structural overview of the plasma membrane Na+,K+-ATPase and H+-ATPase ion pumps

    DEFF Research Database (Denmark)

    Morth, Jens Preben; Pedersen, Bjørn Panella; Buch-Pedersen, Morten Jeppe

    2011-01-01

    transport systems that are responsible for uptake and extrusion of metabolites and other ions. The ion gradients are also both directly and indirectly used to control pH homeostasis and to regulate cell volume. The plasma membrane H(+)-ATPase maintains a proton gradient in plants and fungi and the Na(+),K(+)-ATPase...... maintains a Na(+) and K(+) gradient in animal cells. Structural information provides insight into the function of these two distinct but related P-type pumps.......Plasma membrane ATPases are primary active transporters of cations that maintain steep concentration gradients. The ion gradients and membrane potentials derived from them form the basis for a range of essential cellular processes, in particular Na(+)-dependent and proton-dependent secondary...

  18. State-selective electron capture in collisions of ground and metastable O2+ ions with H(1s)

    International Nuclear Information System (INIS)

    Cabello, C N; Errea, L F; Fernandez, L; Mendez, L; Macias, A; Rabadan, I; Riera, A

    2003-01-01

    An ab initio calculation of the electron capture cross sections for collisions of ground and metastable states of O 2+ with H(1s) is presented. For impact energies between 0.125 and 3.4 keV amu -1 , we find good agreement between the cross sections from the ground state ion with the mixed beam experimental data of Phaneuf et al (Phaneuf A, Alvarez I, Meyer F W and Crandall D H 1982 Phys. Rev. A 26 1892)

  19. Metal impurity transport control in JET H-mode plasmas with central ion cyclotron radiofrequency power injection

    DEFF Research Database (Denmark)

    Valisa, M.; Carraro, L.; Predebon, I.

    2011-01-01

    The scan of ion cyclotron resonant heating (ICRH) power has been used to systematically study the pump out effect of central electron heating on impurities such as Ni and Mo in H-mode low collisionality discharges in JET. The transport parameters of Ni and Mo have been measured by introducing...

  20. Study of the H+, F- and C2O42- ions effect on the Columbo-Tantalites dissolution

    International Nuclear Information System (INIS)

    Rodriguez, Mario; Ruiz, Maria del Carmen

    2003-01-01

    The dissolution reaction of Nb, Ta, Fe and Mn in aqueous solutions of HF, HF-H 2 C 2 O 4 , HF-Na 2 C 2 O 4 and H 2 C 2 O 4 -NaF mixtures, using columbo-tantalites of the San Luis Province, has been studied using a Parr autoclave.The temperature range investigated in this work is between 340 and 396 K.At the moment, the experimental data show that the presence of H + and F - ions in the leaching solution is necessary to produce an appreciable dissolution of columbo-tantalite.Also, the presence of C 2 O 4 2- ions favors the mineral dissolution.On the other hand, both the rise of the H + , F - and C 2 O 4 2- ions concentrations and the increase temperature lead to higher Nb and Ta extractions.Moreover, the presence of the Na + of ion in the leaching media induce the formation of Nb and/or Ta insoluble complexes that settle on the residue

  1. Fivefold Coordination of a CuII–Aqua Ion,[Cu(H2O)5]2+ Complex ...

    Indian Academy of Sciences (India)

    It is generally assumed that a CuII ion in an aqueous solution forms an octahedral [Cu(H2O)6]2+ complex that undergoes Jahn–Teller distortion with elongated axial bonds because of its d9 electronic configuration.

  2. Interpretation of the vibrational energy level structure of the astructural molecular ion H5 + and all of its deuterated isotopomers

    Science.gov (United States)

    Sarka, János; Császár, Attila G.

    2016-04-01

    Variational nuclear motion computations, employing an exact kinetic energy operator and two different potential energy surfaces, are performed to study the first 60 vibrational states of the molecular ion H 5+ ≡ [H2-H-H2]+ and all of its deuterated isotopologues and isotopomers, altogether 12 species. Detailed investigation of the vibrational wavefunctions mostly results in physically intuitive labels not only for the fundamentals but also for the overtone and combination states computed. The torsional motion associated with the left and right diatomics appears to be well separated from the other vibrational degrees of freedom for all species. The unusual structure of the higher-lying bending states and the heavy mixing of the internal motions is partly due to the astructural character of all these molecular ions. The existence of distinct isotopomers in the H 5 - n Dn + , n = 1-4 cases, in the energy range studied, is confirmed. Two rules determine the stability order of the isotopomers: first, when possible, H prefers to stay in the middle of the ions rather than at the sides, and, second, the isotopomer with a homonuclear diatomic at the side is always lower in energy. The large number of precise vibrational energies of the present study, as well as the detailed assignment of the states, should serve as benchmarks for future studies by more approximate nuclear-motion treatments, such as diffusion Monte Carlo and multiconfiguration time-dependent Hartree.

  3. H3+ molecular ion in a magnetic field: Linear parallel configuration

    International Nuclear Information System (INIS)

    Turbiner, A. V.; Guevara, N. L.; Lopez Vieyra, J. C.

    2007-01-01

    A detailed study of the ground state of the H 3 + molecular ion in linear configuration, parallel to the magnetic field direction, and its low-lying Σ, Π, and Δ states is carried out for magnetic fields B=0-4.414x10 13 G in the Born-Oppenheimer approximation. The variational method is employed with a single trial function which includes electronic correlation in the form exp(γr 12 ), where γ is a variational parameter. It is shown that the quantum numbers of the state of the lowest total energy (ground state) depend on the magnetic field strength. The ground state evolves from the spin-singlet 1 Σ g state for weak magnetic fields B(less-or-similar sign)5x10 8 G to a weakly bound spin-triplet 3 Σ u state for intermediate fields and, eventually, to a spin-triplet 3 Π u state for 5x10 10 (less-or-similar sign)B(less-or-similar sign)4.414x10 13 G. Local stability of the linear parallel configuration with respect to possible small deviations is checked

  4. Hydronium-Ion-Catalyzed Elimination Pathways of Substituted Cyclohexanols in Zeolite H-ZSM5

    Energy Technology Data Exchange (ETDEWEB)

    Hintermeier, Peter H. [Department; Eckstein, Sebastian [Department; Mei, Donghai [Institute; Olarte, Mariefel V. [Institute; Camaioni, Donald M. [Institute; Baráth, Eszter [Department; Lercher, Johannes A. [Department; Institute

    2017-10-02

    Hydronium ions in the pores of zeolite H-ZSM5 show high catalytic activity in the elimination of water from cyclohexanol in aqueous phase. Substitution induces subtle changes in rates and reaction pathways, which are concluded to be related to steric effects. Exploring the reaction pathways of 2-, 3-, and 4-methylcyclohexanol (2-McyOH, 3-McyOH, and 4-McyOH), 2- and 4-ethylcyclohexanol (2-EcyOH and 4-EcyOH), 2-n-propylcyclohexanol (2-PcyOH), and cyclohexanol (CyOH) it is shown that the E2 character increases with closer positioning of the alkyl and hydroxyl groups. Thus, 4-McyOH dehydration proceeds via an E1-type elimination, while cis-2-McyOH preferentially reacts via an E2 pathway. The entropy of activation decreased with increasing alkyl chain length (ca. 20 J mol-1 K-1 per CH2 unit) for 2-substituted alcohols, which is concluded to result from constraints influencing the configurational entropy of the transition states.

  5. Angular dependence of the attosecond time delay in the H 2 + ion

    Science.gov (United States)

    Kheifets, Anatoli; Serov, Vladislav

    2016-05-01

    Angular dependence of attosecond time delay relative to polarization of light can now be measured using combination of RABBITT and COLTRIMS techniques. This dependence brings particularly useful information in molecules where it is sensitive to the orientation of the molecular axis. Here we extend the theoretical studies of and consider a molecular ion H2+in combination of an attosecond pulse train and a dressing IR field which is a characteristic set up of a RABBIT measurement. We solve the time-dependent Schrödinger equation using a fast spherical Bessel transformation (SBT) for the radial variable, a discrete variable representation for the angular variables and a split-step technique for the time evolution. The use of SBT ensures correct phase of the wave function for a long time evolution which is especially important in time delay calculations. To speed up computations, we implement an expanding coordinate (EC) system which allows us to reach space sizes and time periods unavailable by other techniques. Australian Research Council DP120101805.

  6. Target thickness dependent convoy electron production of aligned molecular HeH+-ions

    International Nuclear Information System (INIS)

    Kemmler, J.; Groeneveld, K.O.; Heil, O.; Kroneberger, K.; Rothard, H.

    1990-01-01

    Many experiments have shown that the collective excitation of valence electrons effects the alignment and the stopping power of fast diatomic molecular ions penetrating thin solids. Collective excitations also seem to play an important role for the total electron emission induced by fast atomic and molecular ions. For a specific part of the overall electron distribution the convoy electrons, accompanying the projectile ion with equal speed and direction (v 0 ∼ v p ), production mechanism had been proposed which attach their origin to the wake-potential. The authors presented a simple method for the detection of aligned diatomic molecular ions penetrating thin foils. Their first experimental results gave hints that the molecular enhancement for the convoy electron production of molecular ions is not simply a direct effect of the wake potential, but more contributed to the correlated action of the fast projectile ions in the solid

  7. L-H power threshold scaling with magnetic geometry on NSTX and the role of ion orbit loss

    Science.gov (United States)

    Battaglia, D. J.; Chang, C.-S.; Kaye, S. M.; Ku, S.; Maingi, R.; NSTX Team

    2011-10-01

    The L-H power threshold (PLH) on the National Spherical Torus Experiment varies with X-point radius (RX) , plasma current (Ip) , the direction of the ion grad-B drift and the amount of lithium evaporated on the divertor surfaces. The edge Te and Ti (where Te ~ Ti) just prior to the time of the L-H transition vary with the magnetic geometry, but are fairly independent of the neutral fueling rate and lithium conditioning. These observations are consistent with the X-transport theory, which describes the mean edge radial electric field (Er) profile required to prevent non-ambipolar ion loss in a diverted plasma. A guiding-center orbit calculation in the absence of electric fields, collisions and flows provides insight into the dependence of the ion loss, and thus Er, on the magnetic geometry and edge Ti. For example, the number of ion loss orbits remains constant as RX is reduced from 0.64m to 0.47m only if the edge Ti increases by 60%. This is in agreement with self-consistent calculations of Er using the neoclassical XGC0 code and experiments that measured edge Te and Ti to be 40 - 60% larger. Similar agreement is also observed between guiding-center calculations, XGC0 results and the measured PLH versus Ip and ion grad-B direction. Supported by US DOE contracts DE-AC02-09CH11466 and DE-AC05-00OR22725.

  8. Recombination of H{sup +}{sub 3} ions in the afterglow of a He-Ar-H{sub 2} plasma

    Energy Technology Data Exchange (ETDEWEB)

    Glosik, J; Korolov, I; Plasil, R; Novotny, O; Kotrik, T; Hlavenka, P; Varju, J [Mathematics and Physics Faculty, Charles University in Prague, Prague 8 (Czech Republic); Mikhailov, I A; Kokoouline, V [Department of Physics, University of Central Florida, Orlando, FL 32816 (United States); Greene, Chris H [Department of Physics and JILA, University of Colorado, Boulder, CO 80309-0440 (United States)], E-mail: Juraj.Glosik@mff.cuni.cz

    2008-10-14

    Recombination of H{sup +}{sub 3} with electrons is studied in a low-temperature plasma containing He, H{sub 2} and Ar at different He and H{sub 2} densities. The effective plasma recombination rate is driven by binary, H{sup +}{sub 3} + e{sup -}, and ternary, H{sup +}{sub 3} + e{sup -}+ He, processes with the rate coefficients 7.5 x 10{sup -8} cm{sup 3} s{sup -1} and 2.8 x 10{sup -25} cm{sup 6} s{sup -1} respectively at 260 K. We suggest that the ternary recombination involves formation of neutral highly excited Rydberg H{sub 3} followed by an l-changing collision with He. The difference between recombination of para- and ortho-H{sup +}{sub 3} is discussed. (fast track communication)

  9. FAST TRACK COMMUNICATION: Recombination of H+3 ions in the afterglow of a He Ar H2 plasma

    Science.gov (United States)

    Glosik, J.; Korolov, I.; Plasil, R.; Novotny, O.; Kotrik, T.; Hlavenka, P.; Varju, J.; Mikhailov, I. A.; Kokoouline, V.; Greene, Chris H.

    2008-10-01

    Recombination of H+3 with electrons is studied in a low-temperature plasma containing He, H2 and Ar at different He and H2 densities. The effective plasma recombination rate is driven by binary, H+3 + e-, and ternary, H+3 + e-+ He, processes with the rate coefficients 7.5 × 10-8 cm3 s-1 and 2.8 × 10-25 cm6 s-1 respectively at 260 K. We suggest that the ternary recombination involves formation of neutral highly excited Rydberg H3 followed by an l-changing collision with He. The difference between recombination of para- and ortho-H+3 is discussed.

  10. Long-pulse beam acceleration of MeV-class H(-) ion beams for ITER NB accelerator.

    Science.gov (United States)

    Umeda, N; Kashiwagi, M; Taniguchi, M; Tobari, H; Watanabe, K; Dairaku, M; Yamanaka, H; Inoue, T; Kojima, A; Hanada, M

    2014-02-01

    In order to realize neutral beam systems in International Thermonuclear Experimental Reactor whose target is to produce a 1 MeV, 200 A/m(2) during 3600 s D(-) ion beam, the electrostatic five-stages negative ion accelerator so-called "MeV accelerator" has been developed at Japan Atomic Energy Agency. To extend pulse length, heat load of the acceleration grids was reduced by controlling the ion beam trajectory. Namely, the beam deflection due to the residual magnetic field of filter magnet was suppressed with the newly developed extractor with a 0.5 mm off-set aperture displacement. The new extractor improved the deflection angle from 6 mrad to 1 mrad, resulting in the reduction of direct interception of negative ions from 23% to 15% of the total acceleration power, respectively. As a result, the pulse length of 130 A/m(2), 881 keV H(-) ion beam has been successfully extended from a previous value of 0.4 s to 8.7 s. This is the first long pulse negative ion beam acceleration over 100 MW/m(2).

  11. A Facile, Nonreactive Hydrogen Peroxide (H2O2) Detection Method Enabled by Ion Chromatography with UV Detector.

    Science.gov (United States)

    Song, Mingrui; Wang, Junli; Chen, Baiyang; Wang, Lei

    2017-11-07

    Hydrogen peroxide (H 2 O 2 ) is ubiquitous in the natural environment, and it is now widely used for pollutant control in water and wastewater treatment processes. However, current analytical methods for H 2 O 2 inevitably require reactions between H 2 O 2 and other reactants to yield signals and are thus likely subjective to the interferences of coexisting colored, oxidative, and reductive compounds. In order to overcome these barriers, we herein for the first time propose to analyze H 2 O 2 by ion chromatography (IC) using an ultraviolet (UV) detector. The proposal is based on two principles: first, that H 2 O 2 can deprotonate to hydroperoxyl ion (HO 2 - ) when eluent pH is higher than the acid-dissociation coefficient of H 2 O 2 (pK a = 11.6); and second, that after separation from other compounds via IC column, H 2 O 2 can be quantified by a UV detector. Under favorable operating conditions, this method has successfully achieved acceptable recoveries (>91%) of H 2 O 2 dosed to ultrapure and natural waters, a calibration curve with R 2 > 0.99 for a wide range of H 2 O 2 concentrations from 0.1 to 50 mg/L and a method detection limit of 0.027 mg/L. In addition, this approach was shown to be capable of distinguishing H 2 O 2 from anions (e.g., fluoride and chloride) and organics (e.g., glycolate) and monochloramine, suggesting that it is insensitive to many neighboring compounds as long as they do not react quickly with H 2 O 2 . Hence, this study proves the combination of IC and UV detector a facile and reliable method for H 2 O 2 measurement.

  12. Setup and proof of principle of SAPIS (Stored Atoms Polarized Ion Source), a novel source of polarized H-/D- ions

    International Nuclear Information System (INIS)

    Emmerich, R.

    2007-01-01

    The objective of this work was the setup and the proof-of-principle of a new type of negative polarized hydrogen or deuterium ion source, which is based on the charge-exchange reaction vectorH 0 +Cs 0 →vectorH - +Cs + , as for instance the Colliding-Beams-Source (CBS) at the Cooler Synchrotron COSY in Juelich. In contrast to the CBS, the use of a storage cell for the charge-exchange region promises an increase in H - current by at least an order of magnitude without considerable polarization losses. For these purposes, a new laboratory was equipped and both a polarized hydrogen/deuterium atomic beam source and an intense neutral cesium-beam source have been build-on. A Lambshift polarimeter, which allows the measurement of the nuclear polarization of the atomic as well as ionic beams, was completed with the construction of a new spin-filter. After commissioning and optimizing each of these sources, a storage cell was developed and installed in the charge-exchange region with a magnetic field. Additionally, components for the extraction, detection and analysis of the negative ion beam were installed. Following the decisive proof of principle, investigation of the properties of the storage cell, especially as to H recombination and depolarisation, was begun. Furthermore, a number of software programs was developed for the control and monitoring of different components of the sources as well as a universal measuring software for the complete installation, including the measurement and calculation of the beam polarization. At the same time, the remote control system of the Cologne source of polarized ions LASCO at the FN tandem accelerator was completely modernized. (orig.)

  13. Probing the mechanism of H/D exchange between deuterated ammonia and the [M-1]- ions of chlorinated benzene

    International Nuclear Information System (INIS)

    Chan, S.; Enke, C.G.

    1990-01-01

    Hydrogen/deuterium (H/D) exchange reactions have been shown to occur in a CI source between anions of substituted benzene and a number of deuterated reagents. These reactions are of interests because of their potential application for isomer identification using tandem mass spectrometry. The authors have studied H/D exchanges between ND 3 and the [M-1] - ion of chlorinated benzene in the second stage of a triple quadrupole mass spectrometer. The results derived from experiments on 1,2-dichlorobenzene, 1,3-dichlorobenzene and 1,4-dichlorobenzene exhibit maxima of 3, 2 and 1 sequential H/D exchanges, respectively. Higher collisional ND 3 pressure in the second quadrupole favors the formation of products with the maximum number of deuterium substitutions. These experiments strongly suggest that the charge on an [M-1] - reactant ions is localized on one of the carbons of the aromatic ring

  14. Molecular enhancement of Balmer emissions following foil-induced dissociation of fast H2+ and H3+ ions

    International Nuclear Information System (INIS)

    Kobayashi, H.; Oda, N.

    1984-01-01

    Relative emission yields of Balmer lines as functions of the dwell time (t/sub D/ = 0.97--54.1 fs) in thin carbon foils (2--68 μg/cm 2 ) have been measured with (0.2--0.8)-MeV/amu H + , H 2 + , and H 3 + incident on thin carbon foils. Large molecular effects for emission yields of Balmer lines have been observed for H 2 + and H 3 + , where the molecular effect for H 3 + is larger than that for H 2 + . The molecular effects for H 2 + and H 3 + depend on the principal quantum number (n = 3--6), but this n dependence disappears at the largest t/sub D/ ( = 54.1 fs). The molecular effects rapidly decrease with increasing t/sub D/ in the small-t/sub D/ ( or approx. =2 fs) region. The magnitudes of the molecular effects at the largest t/sub D/ ( = 54.1 fs) are in good agreement with those by Andresen et al. [Phys. Scr. 19, 335 (1979)]. Relative populations of n-state hydrogens in the large-t/sub D/ (> or approx. =2 fs) region have been derived from the relative yields of Balmer lines as functions of n and t/sub D/. The molecular enhancement for relative populations of n-state hydrogens for H 2 + depends on n and t/sub D/, and decreases with increasing t/sub D/ and increases with increasing n

  15. The comparison of calcium ion release and pH changes from modified MTA and bioceramics in regeneration

    Science.gov (United States)

    Irawan, R. M.; Margono, A.; Djauhari, N.

    2017-08-01

    The surface reactions of bioactive materials release and change dissolutions triggering intracellular and extracellular responses. Calcium ion release can promote alkalinizing activity, which is needed in tissue regeneration. To analyze calcium ion release and pH changes in modified MTA and bioceramics as bioactive materials. Thirty samples, measuring 3 mm in diameter and 3 mm in height, were prepared, with 15 consisting of modified MTA and 15 consisting of bioceramics. Both materials were immersed in deionized water for an hour, then measured and transferred into fresh solutions and soaked for 48 hours or 168 hours. The measurements were conducted using an atom absorption spectrophotometer and pHmeter. Mann Whitney’s post hoc statistic test showed a significant difference among all the 1-hour, 48-hour, and 168-hour measurement groups, with a value of p ≤ 0.05. Bioceramics released more calcium ions and raised pH levels higher than modified MTA for each of the three soak-time groups. Bioceramics released more calcium ion and had higher pH level compared to modified MTA which contributed to the tissue regeneration.

  16. 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.

  17. Collisions of carbon and oxygen ions with electrons, H, H/sub 2/ and He: Volume 5

    Energy Technology Data Exchange (ETDEWEB)

    Phaneuf, R.A.; Janev, R.K.; Pindzola, M.S.

    1987-02-01

    This report provides a handbook for fusion research of recommended cross-section and rate-coefficient data for collisions of carbon and oxygen ions with electrons, hydrogen atoms and molecules, and helium atoms. Published experimental and theoretical data have been collected and evaluated, and recommended data are presented in tabular, graphical, and parametrized form. Processes considered include exciation, ionization, and charge exchange at collision energies appropriate to applications in fusion-energy research.

  18. Photochemical methodologies for organic waste treatment: advanced oxidation process using uranyl ion with H2O2

    International Nuclear Information System (INIS)

    Naik, D.B.; Sarkar, S.K.; Mukherjee, T.

    2009-01-01

    Excited uranyl ion is able to degrade dyes such as thionine and methylene blue on irradiation with 254 nm/300 nm light. By adding H 2 O 2 along with uranyl ion, photodegradation takes place with visible light and also with enhanced rate. The hydroxyl radicals generated in the reoxidation of U(IV)/UO 2 + to UO 2 2+ are responsible for this enhanced degradation. The above advanced oxidation process (AOP) was applied to study the oxidation of 2-propanol to acetone. (author)

  19. Lifetime measurement of a collision complex using ion cyclotron double resonance - H2C6N2(+)

    Science.gov (United States)

    Anicich, Vincent G.; Sen, Atish D.; Huntress, Wesley T., Jr.; Mcewan, Murray J.

    1991-01-01

    In the ion-molecule reaction between HC3N(+) and HC3N, the lifetime of the collision complex (H2C6N2+)-asterisk was long enough that ion cyclotron double-resonance techniques could be used to probe the distribution of the lifetimes of the collision complex. The mean lifetime of the collision complex at room temperature was measured as 180 microsec with a distribution ranging from 60 to 260 microsec as measured at the half-heights in the distribution. Lifetimes of this magnitude with respect to unimolecular dissociation allow for some stabilization of the collision complex by the slower process of infrared photon emission.

  20. Enhancement of H{sup -}/D{sup -} volume production in a double plasma type negative ion source

    Energy Technology Data Exchange (ETDEWEB)

    Fukumasa, Osamu; Nishimura, Hideki; Sakiyama, Satoshi [Yamaguchi Univ., Ube (Japan). Faculty of Engineering

    1997-02-01

    H{sup -}/D{sup -} production in a pure volume source has been studied. In our double plasma type negative ion source, both energy and density of fast electrons are well controlled. With the use of this source, the enhancement of H{sup -}/D{sup -} production has been observed. Namely, under the same discharge power, the extracted H{sup -}/D{sup -} current in the double plasma operation is higher than that in the single plasma operation. At the same time, measurements of plasma parameters have been made in the source and the extractor regions for these two cases. (author)

  1. Spin diffusion and1H spin-lattice relaxation in Cs2(HSO4)(H2PO4) containing a small amount of ammonium ions.

    Science.gov (United States)

    Hayashi, Shigenobu; Jimura, Keiko

    2017-11-01

    Inorganic solid acid salts with hydrogen bond networks frequently show very long spin-lattice relaxation times even for 1 H because the hydrogen bonds suppress motions. In the present work, the 1 H spin-lattice relaxation in Cs 2 (HSO 4 )(H 2 PO 4 ) containing a small amount of ammonium ions were studied in detail by use of the effect of magic angle spinning (MAS) on the relaxation. The 1 H spin-lattice relaxation times of the acid protons decrease with increase in the content of ammonium ions. Reorientation of the NH 4 group fluctuates the dipole-dipole interaction and relaxes the ammonium protons as well as the acid protons. The 1 H relaxation times of the acid protons are a little bit longer than those of the ammonium protons at the MAS rate of 8 kHz. The spinning at 50 kHz makes the relaxation times of the acid protons longer and those of the ammonium protons shorter. Spin diffusion between the acid and the ammonium protons averages partially the 1 H relaxation of the acid and the ammonium protons at the MAS rate of 8 kHz. The spin diffusion is suppressed completely at the MAS rate of 50 kHz. Spin diffusion between the acid protons is not suppressed at the MAS rate of 50 kHz. The acid protons always show the same relaxation times. The intrinsic relaxation times not affected by spin diffusion are evaluated quantitatively for both the acid and the ammonium protons. Those values are independent of the ammonium content. Contribution of the spin diffusion between the acid and the ammonium protons to the relaxation is estimated quantitatively. Using those parameters, the effect of ammonium ions on the 1 H spin-lattice relaxation can be predicted. The 1 H spin-lattice relaxation is a sensitive tool to study the distribution of ammonium ions in solids. Copyright © 2017 Elsevier Inc. All rights reserved.

  2. Improvement of Current Gain in Triple Ion Implanted 4H-SiC Bipolar Junction Transistor with Etched Extrinsic Base Regions

    Science.gov (United States)

    Tajima, Taku; Nakamura, Tadashi; Satoh, Masataka; Nakamura, Tohru

    We demonstrate triple ion implanted 4H-SiC bipolar junction transistor (BJT). By etching the extrinsic base regions using inductively coupled plasma dry etching, the characteristics of triple ion implanted 4H-SiC BJT were significantly improved. Maximum common emitter current gain was improved from 1.7 to 7.5.

  3. Functional reduced graphene oxide-based membranes with selective ion transport channels for zwitterionic ions separation based on the pH gradient.

    Science.gov (United States)

    Wu, Yu; Ji, Hongyun; Yang, Feng; Meng, Yan; Wang, Yujue; Dai, Jianyuan; Ren, Haisheng; Tan, Guangqun; Xiao, Dan

    2018-01-18

    In this work, we report a method for the fabrication of a functional free-standing graphene membrane (FFGM) with high mechanical strength, enlarged interlayer spacing and ion channels for zwitterionic ions separation. To obtain the FFGM, the anionic dye Eosin Y (EY) was introduced into a graphene oxide (GO) and hydroquinone (HQ) mixture to prepare functional graphene-based membranes on Cu foil using simply a drop-casting method. In comparison with a GO membrane, the molar flux and the mechanical strength of the FFGM were dramatically increased. The FFGM was then equipped on custom-built glass reservoirs for zwitterionic amino acids (AAs) separation based on the inner pH gradient, which was formed by controlling H + and OH - (in the feed and receiver solution) migration in rGO/GO sheets via an external electric field. With the help of the inner pH gradient and external electric field, AAs could change their charge behaviors. The ionized AAs transport through the FFGM and finally separation was realized.

  4. H2O2 assisted room temperature oxidation of Ti2C MXene for Li-ion battery anodes

    KAUST Repository

    Ahmed, Bilal

    2016-03-08

    Herein we demonstrate that a prominent member of the MXene family, Ti2C, undergoes surface oxidation at room temperature when treated with hydrogen peroxide (H2O2). The H2O2 treatment results in opening up of MXene sheets and formation of TiO2 nanocrystals on their surface, which is evidenced by the high surface area of H2O2 treated MXene and X-ray diffraction (XRD) analysis. We show that the reaction time and the amount of hydrogen peroxide used are the limiting factors, which determine the morphology and composition of the final product. Furthermore, it is shown that the performance of H2O2 treated MXene as an anode material in Li ion batteries (LIBs) was significantly improved as compared to as-prepared MXenes. For instance, after 50 charge/discharge cycles, specific discharge capacities of 389 mA h g−1, 337 mA h g−1 and 297 mA h g−1 were obtained for H2O2 treated MXene at current densities of 100 mA g−1, 500 mA g−1 and 1000 mA g−1, respectively. In addition, when tested at a very high current density, such as 5000 mA g−1, the H2O2 treated MXene showed a specific capacity of 150 mA h g−1 and excellent rate capability. These results clearly demonstrate that H2O2 treatment of Ti2C MXene improves MXene properties in energy storage applications, such as Li ion batteries or capacitors.

  5. Nanostructural evolution and behavior of H and Li in ion-implanted γ-LiAlO 2

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Weilin; Zhang, Jiandong; Edwards, Danny J.; Overman, Nicole R.; Zhu, Zihua; Price, Lloyd; Gigax, Jonathan; Castanon, Elizabeth; Shao, Lin; Senor, David J.

    2017-10-01

    In-situ He+ ion irradiation is performed under a helium ion microscope to study nanostructural evolution in polycrystalline gamma-LiAlO2 pellets. Various locations within a grain, across grain boundaries and at a cavity are selected. The results exhibit He bubble formation, grain-boundary cracking, nanoparticle agglomeration, increasing surface brightness with dose, and material loss from the surface. Similar brightening effects at grain boundaries are also observed under a scanning electron microscope. Li diffusion and loss from polycrystalline gamma-LiAlO2 is faster than its monocrystalline counterpart during H2+ ion implantation at elevated temperatures. There is also more significant H diffusion and release from polycrystalline pellets during thermal annealing of 300 K implanted samples. Grain boundaries and cavities could provide a faster pathway for H and Li diffusion. H release is slightly faster from the 573 K implanted monocrystalline gamma-LiAlO2 during annealing at 773 K. Metal hydrides could be formed preferentially along the grain boundaries to immobilize hydrogen.

  6. Production of Long-Lived H2-, HD-, and D2- during Grazing Scattering Collisions of H2+, H3+, D2+, D3+ and D2H+ Ions with KBr, KCl, and LiF Surfaces

    International Nuclear Information System (INIS)

    Seely, D. G.; Meyer, F. W.; Zhang, H.; Havener, C. C.

    2009-01-01

    We have investigated atomic and molecular anion production from singly charged atomic and molecular hydrogen, deuterium, and mixed isotope beams during grazing interactions with large area KBr, KCl, and LiF single crystal targets in the incident energy range 4-22.5 keV. Electron capture and, in the case of incident molecular ions, dissociation occur during the grazing interactions without appreciable angular straggling or change in velocity. As a result, atomic and molecular cation and anion interaction products are strongly peaked in the specular reflection direction, and, in case of dissociation products, at the fractional kinetic energies determined by the product fragment mass to incident mass ratios. A large-acceptance electrostatic analysis and detection system is used to collect the charged scattering products with high efficiency. Of particular interest is the production of metastable molecular ions H 2 - , HD - , and D 2 - . By comparing molecular anion yields obtained from incident hydrogen, deuterium and mixed isotope molecular ions, effects arising from isobaric contamination are seen for some incident molecular species.

  7. Efficiency of Cs-free materials for negative ion production in H2 and D2 plasmas

    Science.gov (United States)

    Friedl, R.; Kurutz, U.; Fantz, U.

    2017-08-01

    High power negative ion sources use caesium to reduce the work function of the converter surface which significantly increases the negative ion yield. Caesium, however, is a very reactive alkali-metal and shows complex redistribution dynamics in consequence of plasma-surface-interaction. Thus, maintaining a stable and homogenous low work function surface is a demanding task, which is not easily compatible with the RAMI issues (reliability, availability, maintainability, inspectability) for a future DEMO fusion reactor. Hence, Cs-free alternative materials for efficient negative ion formation are desirable. At the laboratory experiment HOMER materials which are referred to as promising are investigated under identical and ion source relevant parameters: the refractory metals Ta and W, non-doped and boron-doped diamond as well as materials with inherent low work function (lanthanum-doped molybdenum, MoLa and lanthanum hexaboride, LaB6). The results are compared to the effect of in-situ caesiation, which at HOMER leads to a maximal increase of the negative ion density by a factor of 2.5. Among the examined samples low work function materials are most efficient. In particular, MoLa leads to an increase of almost 50 % compared to pure volume formation. The difference to a caesiated surface can be attributed to the still higher work function of MoLa, which is expected to be slightly below 3 eV. Using deuterium instead of hydrogen leads to increased atomic and positive ion densities, while comparable negative ion densities are achieved. In contrast to the low work function materials, bulk samples of the refractory metals as well as carbon based materials have no enhancing effect on H-, where the latter materials furthermore show severe erosion due to the hydrogen plasma.

  8. Long pulse acceleration of MeV class high power density negative H{sup −} ion beam for ITER

    Energy Technology Data Exchange (ETDEWEB)

    Umeda, N., E-mail: umeda.naotaka@jaea.go.jp; Kojima, A.; Kashiwagi, M.; Tobari, H.; Hiratsuka, J.; Watanabe, K.; Dairaku, M.; Yamanaka, H.; Hanada, M. [Japan Atomic Energy Agency, 801-1 Mukouyama, Naka-shi, Ibaraki 311-0193 Japan (Japan)

    2015-04-08

    R and D of high power density negative ion beam acceleration has been carried out at MeV test facility in JAEA to realize ITER neutral beam accelerator. The main target is H{sup −} ion beam acceleration up to 1 MeV with 200 A/m{sup 2} for 60 s whose pulse length is the present facility limit. For long pulse acceleration at high power density, new extraction grid (EXG) has been developed with high cooling capability, which electron suppression magnet is placed under cooling channel similar to ITER. In addition, aperture size of electron suppression grid (ESG) is enlarged from 14 mm to 16 mm to reduce direct interception on the ESG and emission of secondary electron which leads to high heat load on the upstream acceleration grid. By enlarging ESG aperture, beam current increased 10 % at high current beam and total acceleration grid heat load reduced from 13 % to 10 % of input power at long pulse beam. In addition, heat load by back stream positive ion into the EXG is measured for the first time and is estimated as 0.3 % of beam power, while heat load by back stream ion into the source chamber is estimated as 3.5 ~ 4.0 % of beam power. Beam acceleration up to 60 s which is the facility limit, has achieved at 683 keV, 100 A/m{sup 2} of negative ion beam, whose energy density increases two orders of magnitude since 2011.

  9. Design, operational experiences and beam results obtained with the SNS H- ion source and LEBT at Berkeley Lab

    International Nuclear Information System (INIS)

    Keller, R.; Thomae, R.; Stockli, M.; Welton, R.

    2002-01-01

    The ion source and Low-Energy Transport (LEBT) system that will provide H - ion beams to the Spallation Neutron Source (SNS)** Front End and the accelerator chain have been developed into a mature unit that fully satisfies the operational requirements through the commissioning and early operating phases of SNS. Compared to the early R and D version, many features of the ion source have been improved, and reliable operation at 6% duty factor has been achieved producing beam currents in the 35-mA range and above. LEBT operation proved that the purely electrostatic focusing principle is well suited to inject the ion beam into the RFQ accelerator, including the steering and pre-chopping functions. This paper will discuss the latest design features of the ion source and LEBT, give performance data for the integrated system, and report on commissioning results obtained with the SNS RFQ and Medium-Energy Beam Transport (MEBT) system. Prospects for further improvements will be outlined in concluding remarks

  10. A structural overview of the plasma membrane Na+,K+-ATPase and H+-ATPase ion pumps

    DEFF Research Database (Denmark)

    Morth, Jens Preben; Pedersen, Bjørn Panella; Buch-Pedersen, Morten Jeppe

    2011-01-01

    Plasma membrane ATPases are primary active transporters of cations that maintain steep concentration gradients. The ion gradients and membrane potentials derived from them form the basis for a range of essential cellular processes, in particular Na(+)-dependent and proton-dependent secondary tran......(+)-ATPase maintains a Na(+) and K(+) gradient in animal cells. Structural information provides insight into the function of these two distinct but related P-type pumps....... transport systems that are responsible for uptake and extrusion of metabolites and other ions. The ion gradients are also both directly and indirectly used to control pH homeostasis and to regulate cell volume. The plasma membrane H(+)-ATPase maintains a proton gradient in plants and fungi and the Na(+),K......Plasma membrane ATPases are primary active transporters of cations that maintain steep concentration gradients. The ion gradients and membrane potentials derived from them form the basis for a range of essential cellular processes, in particular Na(+)-dependent and proton-dependent secondary...

  11. Transungual iontophoresis of lithium and sodium: effect of pH and co-ion competition on cationic transport numbers.

    Science.gov (United States)

    Dutet, Julie; Delgado-Charro, M Begoña

    2010-06-01

    Iontophoresis has been proposed as an alternative method to deliver drugs into and across the nail plate. However, the knowledge about the rules governing transungual iontophoretic transport numbers is still uncomplete. This work investigated the iontophoretic and passive transungual fluxes of sodium and lithium and the effect of pH and co-ion competition on the cations' transport numbers. The objective was to further investigate whether nails show cation permselectivity at physiological pH and to improve our understanding of transport numbers during transungual iontophoresis. The donor solutions comprised the single ion and binary mixtures of the two cations at different pH. Sodium and lithium iontophoretic fluxes showed low inter-nail variability and were significantly greater than passive fluxes. Cationic transport numbers clearly increased as the pH was sequentially raised from 4.0 to 5.0 and then to 7.0, in agreement with a net negative charge of the human nails at physiological pH. Sodium transport number was maximal when the ion was formulated as a single ion (absence of competing co-ions) and decreased as the molar fraction of lithium was increased in the vehicle. The magnitude of the transport numbers measured and their response to changes in the cations' molar fraction and pH in the donor solution were remarkably similar to those observed during the transdermal iontophoresis. The ratio of lithium and sodium transport numbers was directly proportional to their relative concentration ratios; the proportionality constant being remarkably similar in the 4.0-7.0 pH range as well as to the ratio of the cations' aqueous mobilities. Another interesting similarity with transdermal iontophoresis was the existence of a cationic transport number threshold. On the whole, this work provided some key information about nail permselectivity and transungual transport numbers which will assist to formulate efficiently therapeutic compounds to be delivered iontophoretically

  12. Analytic cross sections for collisions of H, H2, He and Li Atoms and ions with atoms and molecules. 2

    International Nuclear Information System (INIS)

    Ito, Rinsuke; Tabata, Tatsuo; Shirai, Toshizo; Phaneuf, R.A.

    1994-07-01

    Analytic expressions fitted to Barnett's recommended data are given for the cross sections of excitation and spectral line emission by H, H + , He + , He, and He 2+ colliding with atoms and molecules. The expressions use the semiempirical functional forms proposed by Green and McNeal and some modified forms to make it possible not only to interpolate but also to extrapolate the recommended data. (author)

  13. Fabrication of Silicon Nitride Ion Sensitive Field-Effect Transistor for pH Measurement and DNA Immobilization/Hybridization

    Directory of Open Access Journals (Sweden)

    U. Hashim

    2013-01-01

    Full Text Available The fabrication of ion sensitive field-effect transistor (ISFET using silicon nitride (Si3N4 as the sensing membrane for pH measurement and DNA is reported. For the pH measurement, the Ag/AgCl electrode was used as the reference electrode, and different pH values of buffer solution were used in the ISFET analysis. The ISFET device was tested with pH buffer solutions of pH2, pH3, pH7, pH8, and pH9. The results show that the IV characteristic of ISFET devices is directly proportional and the device’s sensitivity was 43.13 mV/pH. The ISFET is modified chemically to allow the integration with biological element to form a biologically active field-effect transistor (BIOFET. It was found that the DNA immobilization activities which occurred on the sensing membrane caused the drain current to drop due to the negatively charged backbones of the DNA probes repelled electrons from accumulating at the conducting channel. The drain current was further decreased when the DNA hybridization took place.

  14. H+ and Na+ Ion Transport Properties of Sulfonated Poly(2,6-dimethyl-1,4-phenyleneoxide)Membranes

    Czech Academy of Sciences Publication Activity Database

    Bouzek, K.; Moravcová, S.; Samec, Zdeněk; Schauer, Jan

    2003-01-01

    Roč. 150, č. 6 (2003), s. E329-E336 ISSN 0013-4651 R&D Projects: GA ČR GA203/99/0575; GA ČR GA104/02/0664 Institutional research plan: CEZ:AV0Z4050913; CEZ:AV0Z4040901 Keywords : H+ and Na+ ion * sulfonated * membranes Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.361, year: 2003

  15. Elimination of carbon vacancies in 4H-SiC epi-layers by near-surface ion implantation: Influence of the ion species

    Science.gov (United States)

    Ayedh, H. M.; Hallén, A.; Svensson, B. G.

    2015-11-01

    The carbon vacancy (VC) is a prevailing point defect in high-purity 4H-SiC epitaxial layers, and it plays a decisive role in controlling the charge carrier lifetime. One concept of reducing the VC-concentration is based on carbon self-ion implantation in a near surface layer followed by thermal annealing. This leads to injection of carbon interstitials (Ci's) and annihilation of VC's in the epi-layer "bulk". Here, we show that the excess of C atoms introduced by the self-ion implantation plays a negligible role in the VC annihilation. Actually, employing normalized implantation conditions with respect to displaced C atoms, other heavier ions like Al and Si are found to be more efficient in annihilating VC's. Concentrations of VC below ˜2 × 1011 cm-3 can be reached already after annealing at 1400 °C, as monitored by deep-level transient spectroscopy. This corresponds to a reduction in the VC-concentration by about a factor of 40 relative to the as-grown state of the epi-layers studied. The negligible role of the implanted species itself can be understood from simulation results showing that the concentration of displaced C atoms exceeds the concentration of implanted species by two to three orders of magnitude. The higher efficiency for Al and Si ions is attributed to the generation of collision cascades with a sufficiently high energy density to promote Ci-clustering and reduce dynamic defect annealing. These Ci-related clusters will subsequently dissolve during the post-implant annealing giving rise to enhanced Ci injection. However, at annealing temperatures above 1500 °C, thermodynamic equilibrium conditions start to apply for the VC-concentration, which limit the net effect of the Ci injection, and a competition between the two processes occurs.

  16. Electron capture by He2+ ions in collisions with H and H2 at impact energies below 10 keV

    International Nuclear Information System (INIS)

    Nutt, W.L.; McCullough, R.W.; Brady, K.; Shah, M.B.; Gilbody, H.B.

    1978-01-01

    Total cross sections for the process He 2+ + H(1s) → He + (Σn, 1) + H + involving capture into all final bound states of He + have been determined for 3 He 2+ ions in the range 1.5-9.0 keV using a furnace-target technique previously employed for similar measurements at higher impact energies. Measured cross sections are considerably smaller than those measured previously by Fite et al (Proc. R.Soc.; A268:527 (1962)) and are in better accord with recent theoretical estimates. A likely explanation for the discrepancy is given in terms of the corresponding cross sections for electron capture in He 2+ -H 2 collisions which have also been determined. (author)

  17. Synergistic effect of polyaspartic acid and iodide ion on corrosion inhibition of mild steel in H2SO4

    International Nuclear Information System (INIS)

    Qian, Bei; Wang, Jing; Zheng, Meng; Hou, Baorong

    2013-01-01

    Highlights: •Polyaspartic acid acts as a modest cathodic inhibitor for mild steel in H 2 SO 4 . •Results revealed synergistic effect between polyaspartic acid and iodide ion. •Inhibition efficiency depends on the temperature of H 2 SO 4 medium. •XPS analysis revealed co-adsorption of polyaspartic acid and iodide ion. -- Abstract: The inhibition effect of polyaspartic acid (PASP) and its synergistic effect with KI on mild steel corrosion in 0.5 M H 2 SO 4 solution are studied by weight loss and electrochemical methods. The inhibition efficiency increases with the concentration of PASP and increases further with the presence of 1 mM KI. Result of the zero charge potential measurement shows that iodide ion promotes the film formation of PASP greatly. The mild steel surfaces after immersion test were analyzed using scanning electron microscopy and X-ray photoelectron spectroscopy. An adsorption model is proposed to elucidate the synergistic mechanism of synergistic effect

  18. H$^{-}$ ion source for CERN's Linac4 accelerator: simulation, experimental validation and optimization of the hydrogen plasma

    CERN Document Server

    Mattei, Stefano; Lettry, Jacques

    2017-07-25

    Linac4 is the new negative hydrogen ion (H$^-$) linear accelerator of the European Organization for Nuclear Research (CERN). Its ion source operates on the principle of Radio-Frequency Inductively Coupled Plasma (RF-ICP) and it is required to provide 50~mA of H$^-$ beam in pulses of 600~$\\mu$s with a repetition rate up to 2 Hz and within an RMS emittance of 0.25~$\\pi$~mm~mrad in order to fullfil the requirements of the accelerator. This thesis is dedicated to the characterization of the hydrogen plasma in the Linac4 H$^-$ ion source. We have developed a Particle-In-Cell Monte Carlo Collision (PIC-MCC) code to simulate the RF-ICP heating mechanism and performed measurements to benchmark the fraction of the simulation outputs that can be experimentally accessed. The code solves self-consistently the interaction between the electromagnetic field generated by the RF coil and the resulting plasma response, including a kinetic description of charged and neutral species. A fully-implicit implementation allowed to si...

  19. Relative clinical effectiveness of carbon ion radiotherapy. Theoretical modelling for H and N tumours

    International Nuclear Information System (INIS)

    Antonovic, Laura; Toma-Dasu, Iuliana; Dasu, Alexandru; Furusawa, Yoshiya

    2015-01-01

    Comparison of the efficiency of photon and carbon ion radiotherapy (RT) administered with the same number of fractions might be of limited clinical interest, since a wide range of fractionation patterns are used clinically today. Due to advanced photon treatment techniques, hypofractionation is becoming increasingly accepted for prostate and lung tumours, whereas patients with head and neck tumours still benefit from hyperfractionated treatments. In general, the number of fractions is considerably lower in carbon ion RT. A clinically relevant comparison would be between fractionation schedules that are optimal within each treatment modality category. In this in silico study, the relative clinical effectiveness (RCE) of carbon ions was investigated for human salivary gland tumours, assuming various radiation sensitivities related to their oxygenation. The results indicate that, for hypoxic tumours in the absence of reoxygenation, the RCE (defined as the ratio of D 50 for photons to carbon ions) ranges from 3.5 to 5.7, corresponding to carbon ion treatments given in 36 and 3 fractions, respectively, and 30 fractions for photons. Assuming that interfraction local oxygenation changes take place, results for RCE are lower than that for an oxic tumour if only a few fractions of carbon ions are used. If the carbon ion treatment is given in more than 12 fractions, the RCE is larger for the hypoxic than for the well-oxygenated tumour. In conclusion, this study showed that in silico modelling enables the study of a wide range of factors in the clinical considerations and could be an important step towards individualisation of RT treatments. (author)

  20. Experimental dosimetric comparison of 1H, 4He, 12C and 16O scanned ion beams

    Science.gov (United States)

    Tessonnier, T.; Mairani, A.; Brons, S.; Haberer, T.; Debus, J.; Parodi, K.

    2017-05-01

    At the Heidelberg Ion Beam Therapy Center, scanned helium and oxygen ion beams are available in addition to the clinically used protons and carbon ions for physical and biological experiments. In this work, a study of the basic dosimetric features of the different ions is performed in the entire therapeutic energy range. Depth dose distributions are investigated for pencil-like beam irradiation, with and without a modulating ripple filter, focusing on the extraction of key Bragg curve parameters, such as the range, the peak-width and the distal 80%-20% fall-off. Pencil-beam lateral profiles are measured at different depths in water, and parameterized with multiple Gaussian functions. A more complex situation of an extended treatment field is analyzed through a physically optimized spread-out Bragg peak, delivered with beam scanning. The experimental results of this physical beam characterization indicate that helium ions could afford a more conformal treatment and in turn, increased tumor control. This is mainly due to a smaller lateral scattering than with protons, leading to better lateral and distal fall-off, as well as a lower fragmentation tail compared to carbon and oxygen ions. Moreover, the dosimetric dataset can be used directly for comparison with results from analytical dose engines or Monte Carlo codes. Specifically, it was used at the Heidelberg Ion Beam Therapy Center to generate a new input database for a research analytical treatment planning system, as well as for validation of a general purpose Monte Carlo program, in order to lay the groundwork for biological experiments and further patient planning studies.

  1. Electron capture in low- and intermediate-energy collisions between completely stripped light ions and metastable H(2s) targets

    International Nuclear Information System (INIS)

    Blanco, S.A.; Falcon, C.A.; Reinhold, C.O.; Casaubon, J.I.; Piacentini, R.D.

    1987-01-01

    Total cross sections for electron capture from H(2s) targets by He 2+ ions have been computed in the impact velocity range 0.05-0.5 au. Calculations were performed using a molecular close-coupling approach with inclusion of electron translation factors. A ten-state molecular basis set was considered. A comparison is made with Landau-Zener results for the same system. Intermediate projectile energy classical Monte Carlo capture cross sections are also presented for H + , He 2+ , Li 3+ and C 6+ projectiles. (author)

  2. Second-order interference in collisions of 4-MeV/u F9+ ions with H2

    Science.gov (United States)

    Misra, Deepankar; Kelkar, Aditya H.; Chatterjee, Shyamal; Tribedi, Lokesh C.

    2009-12-01

    Frequency doubling in interference oscillations in fast-ion-induced electron emission spectrum from H2 is investigated. Experimentally observed oscillatory structure is well explained by a model calculation based on the rescattering of emitted electron from the second H center. The second-order contribution is found to be as large as 10%. The doubling of oscillation frequency is found out to be independent of angle of observation. Derived analytical expression for the double differential cross section ratio including the first- and second-order interference terms, fits the observed oscillatory structure quite well. The present analysis is in broad agreement with the earlier observations by Stolterfoht

  3. Investigation of the retention/pH profile of zwitterionic fluoroquinolones in reversed-phase and ion-interaction high performance liquid chromatography.

    Science.gov (United States)

    Pistos, C; Tsantili-Kakoulidou, A; Koupparis, M

    2005-09-15

    The retention/pH profiles of three fluoroquinolones, ofloxacin, norfloxacin and ciprofloxacin, was investigated by means of reversed-phase high performance liquid chromatography (RP-HPLC) and reversed-phase ion-interaction chromatography (RP-IIC), using an octadecylsilane stationary phase and acetonitrile as organic modifier. Sodium hexanesulphonate and tetrabutylammonium hydroxide were used as sources of counter ions in ion-interaction chromatography. The retention/pH profiles under in RP-HPLC were compared to the corresponding lipophilicity/pH profiles. Despite the rather hydrophilic nature of the three fluoroquinolones positive retention factors were obtained while there was a shift of the retention maximum towards more acidic pH values. This behavior was attributed mainly to non-hydrophobic silanophilic interactions with the silanized silica gel material of the stationary phase. In ion-interaction chromatography the effect of counter ions over a broad pH range was found to be ruled rather by the ion pair formation in the mobile phase which led to a drastic decrease in retention as a consequence of the disruption of the zwitterionic structure and thereupon the deliberation of a net charge in the molecules. At pH values at which zwitterionic structure was not favored both the ion-exchange and ion pair formation mechanisms were assumed to contribute to the retention.

  4. A kinetic study of Ca-containing ions reacting with O, O2, CO2 and H2O: implications for calcium ion chemistry in the upper atmosphere.

    Science.gov (United States)

    Broadley, Sarah; Vondrak, Tomas; Wright, Timothy G; Plane, John M C

    2008-09-14

    A series of gas-phase reactions involving molecular Ca-containing ions was studied by the pulsed laser ablation of a calcite target to produce Ca+ in a fast flow of He, followed by the addition of reagents downstream and detection of ions by quadrupole mass spectrometry. Most of the reactions that were studied are important for describing the chemistry of meteor-ablated calcium in the earth's upper atmosphere. The following rate coefficients were measured: k(CaO+ + O --> Ca+ + O2) = (4.2 +/- 2.8) x 10(-11) at 197 K and (6.3 +/- 3.0) x 10(-11) at 294 K; k(CaO+ + CO --> Ca+ + CO2, 294 K) = (2.8 +/- 1.5) x 10(-10); k(Ca+.CO2 + O2 --> CaO2+ + CO2, 294 K) = (1.2 +/- 0.5) x10(-10); k(Ca+.CO2 + H2O --> Ca+.H2O + CO2) = (13.0 +/- 4.0) x 10(-10); and k(Ca+.H2O + O2 --> CaO2+ + H2O, 294 K) = (4.0 +/- 2.5) x 10(-10) cm3 molecule(-1) s(-1). The quoted uncertainties are a combination of the 1 sigma standard errors in the kinetic data and the systematic errors in the models used to extract the rate coefficients. Rate coefficients were also obtained for the following recombination (also termed association) reactions in He bath gas: k(Ca+.CO2 + CO2 --> Ca+.(CO2)2, 294 K) = (2.6 +/- 1.0) x 10(-29); k(Ca+.H2O + H2O --> Ca+.(H2O)2) = (1.6 +/- 1.1) x 10(-27); and k(CaO2+ + O2 --> CaO2+.O2) high level quantum chemistry calculations and RRKM theory using an inverse Laplace transform solution of the master equation. The surprisingly slow reaction between CaO+ and O was explained using quantum chemistry calculations on the lowest 2A', 2A'' and 4A'' potential energy surfaces. These calculations indicate that reaction mostly occurs on the 2A' surface, leading to production of Ca+ (2S) + O2(1 Delta g). The importance of this reaction for controlling the lifetime of Ca+ in the upper mesosphere and lower thermosphere is then discussed.

  5. Evaluation of calcium ion release and change in pH on combining calcium hydroxide with different vehicles

    Directory of Open Access Journals (Sweden)

    Charu Grover

    2014-01-01

    Full Text Available Introduction: Intracanal medicaments have traditionally been used in endodontics to disinfect root canals between appointments. Calcium hydroxide is widely used as an intracanal medicament for disinfection and to promote periapical healing. It is stable for long periods, harmless to the body, and bactericidal in a limited area. The efficacy of calcium hydroxide as a disinfectant is dependent on the availability of the hydroxyl ions in the solution that depends on the vehicle in which the calcium hydroxide is carried. In general, three types of vehicles are used: Aqueous, viscous or oily. Some in vitro studies have shown that the type of vehicle has a direct relationship with the concentration and the velocity of ionic liberation as well as with the antibacterial action when the paste is carried into a contaminated area. Aim of the Study: To evaluate the calcium ion release and measure the change in pH of the environment that occurred when calcium hydroxide was combined with different vehicles (distilled water, propylene glycol, calcium hydroxide containing gutta-percha points and chitosan over different time periods. Materials and Methods: Forty single rooted mandibular first premolar teeth were decoronated for this study. Working length was established and the root canals were enlarged and irrigation accomplished with 2 ml of NaOCl solution after every file. The teeth were then randomly divided into four groups. The canals were then packed with different preparations of calcium hydroxide using the following vehicles-distilled water, propylene glycol, gutta-percha points and chitosan. Calcium ion release in different groups was analyzed using an ultraviolet spectrophotometer at 220 nm. The change in pH of was determined using a pH meter. Results were statistically evaluated using one-way ANOVA test. Result: For calcium ion release, Group 2 showed cumulative drug release of 81.97% at the end of 15 days, whereas Group 1, 3 and 4 showed a release

  6. Ion-molecule interactions in crossed-beams. [N/sup +/-H/sub 2/; F/sup +/-H; CO/sub 2//sup +/-D/sub 2/

    Energy Technology Data Exchange (ETDEWEB)

    Hansen, S.G.

    1980-09-01

    Interactions of the ions N/sup +/, F/sup +/, and CO/sub 2//sup +/ with H/sub 2/ and/or its isotopes were examined using the crossed-beam technique in the low (< 4 eV) initial relative energy. For the reaction N/sup +/(/sup 3/P) + H/sub 2/ ..-->.. NH/sup +/ + H, complex formation dominates up to 1.9 eV and a substantial interaction occurs between all collision partners up to 3.6 eV. The distribution of N/sup +/ scattered nonreactively from H/sub 2/ also showed a long-lived complex channel below 1.9 eV. The reaction F/sup +/(/sup 3/P) + H/sub 2/ ..-->..FH/sup +/ + H proceeded by a direct reaction mechanism at 0.20 to 1.07 eV. The reaction CO/sub 2//sup +/ + D/sub 2/ ..-->.. DCO/sub 2//sup +/ + D gives asymmetric product distributions at 0.27 eV and above, indicating a direct reaction mechanism. Results indicated that there are probably barriers in the exit channels for DCO/sub 2//sup +/, DCO/sup +/, and D/sub 2/O/sup +/ products. The electronic state distributions of the N/sup +/, F/sup +/, and CO/sub 2//sup +/ beams was investigated using beam attenuation and total luminescence techniques.

  7. Near-surface recrystallization of the amorphous implanted layer of ion implanted 6H-SiC

    Science.gov (United States)

    Kuhudzai, R. J.; van der Berg, N. G.; Malherbe, J. B.; Hlatshwayo, T. T.; Theron, C. C.; Buys, A. V.; Botha, A. J.; Wendler, E.; Wesch, W.

    2014-08-01

    The recrystallization and subsequent crystal growth during annealing of amorphous surface layers on 6H-SiC produced by ion implantation is investigated. Amorphous surface layers were produced by ion implantation of 360 keV ions of iodine, silver, xenon, cesium and strontium into single crystalline 6H-silicon carbide samples. The ion fluence for all the implantations were in the order of 1016 cm-2. Vacuum annealing of the damaged silicon carbide samples was then performed. The microstructure of SiC surfaces before and after annealing was investigated using a high resolution field emission scanning electron microscope (SEM). SEM analysis was complimented by Atomic Force Microscopy (AFM). SEM images acquired by an in-lens detector using an accelerating voltage of 2 kV show nano-crystallites developed for all implanted samples after annealing. Larger and more faceted crystallites along with elongated thin crystallites were observed for iodine and xenon implanted 6H-SiC. Crystallites formed on surfaces implanted with strontium and cesium were smaller and less faceted. Strontium, silver and cesium implanted samples also exhibited more cavities on the surface. AFM was used to evaluate the effect of annealing on the surface roughness. For all the amorphous surfaces which were essentially featureless, the root mean square (rms) roughness was approximately 1 nm. The roughness increased to approximately 17 nm for the iodine implanted sample after annealing with the surface roughness below this value for all the other samples. AFM also showed that the largest crystals grew to heights of about 17, 20, 45, 50 and 65 nm for Sr, Cs, Ag, Xe and I implanted samples after annealing at 1200 °C for 5 h respectively. SEM images and AFM analysis suggest that iodine is more effective in promoting crystal growth during the annealing of bombardment-induced amorphous SiC layers than the rest of the ions we implanted. In samples of silicon carbide co-implanted with iodine and silver, few

  8. The front end test stand high performance H- ion source at Rutherford Appleton Laboratory.

    Science.gov (United States)

    Faircloth, D C; Lawrie, S; Letchford, A P; Gabor, C; Wise, P; Whitehead, M; Wood, T; Westall, M; Findlay, D; Perkins, M; Savage, P J; Lee, D A; Pozimski, J K

    2010-02-01

    The aim of the front end test stand (FETS) project is to demonstrate that chopped low energy beams of high quality can be produced. FETS consists of a 60 mA Penning Surface Plasma Ion Source, a three solenoid low energy beam transport, a 3 MeV radio frequency quadrupole, a chopper, and a comprehensive suite of diagnostics. This paper details the design and initial performance of the ion source and the laser profile measurement system. Beam current, profile, and emittance measurements are shown for different operating conditions.

  9. Influence of pH on the adsorption of uranium ions by oxidized activated carbon and chitosan

    International Nuclear Information System (INIS)

    Park, G.I.; Park, H.S.; Woo, S.I.

    1999-01-01

    The adsorption characteristics of uranyl ions on surface-oxidized carbon were compared with those of powdered chitosan over a wide pH range. In particular, an extensive analysis was made on solution pH variation during the adsorption process or after adsorption equilibrium. Uranium adsorption on the two adsorbents was revealed to be strongly dependent on the initial pH of the solution. A quantitative comparison of the adsorption capacities of the two adsorbents was made, based on the isotherm data obtained at initial pH 3, 4, and 5. In order to analyze the adsorption kinetics incorporated with pH effects, batch experiments at various initial pH values were carried out, and solution pH profiles with the adsorption time were also evaluated. The breakthrough behavior in a column packed with oxidized carbon was also characterized with respect to the variation of effluent pH. Based on these experimental results, the practical applicability of oxidized carbon for uranium removal from acidic radioactive liquid waste was suggested

  10. Sensing local pH and ion concentration at graphene electrode surfaces using in situ Raman spectroscopy.

    Science.gov (United States)

    Shi, Haotian; Poudel, Nirakar; Hou, Bingya; Shen, Lang; Chen, Jihan; Benderskii, Alexander V; Cronin, Stephen B

    2018-02-01

    We report a novel approach to probe the local ion concentration at graphene/water interfaces using in situ Raman spectroscopy. Here, the upshifts observed in the G band Raman mode under applied electrochemical potentials are used to determine the charge density in the graphene sheet. For voltages up to ±0.8 V vs. NHE, we observe substantial upshifts in the G band Raman mode by as much as 19 cm -1 , which corresponds to electron and hole carrier densities of 1.4 × 10 13 cm -2 and Fermi energy shifts of ±430 meV. The charge density in the graphene electrode is also measured independently using the capacitance-voltage characteristics (i.e., Q = CV), and is found to be consistent with those measured by Raman spectroscopy. From charge neutrality requirements, the ion concentration in solution per unit area must be equal and opposite to the charge density in the graphene electrode. Based on these charge densities, we estimate the local ion concentration as a function of electrochemical potential in both pure DI water and 1 M KCl solutions, which span a pH range from 3.8 to 10.4 for pure DI water and net ion concentrations of ±0.7 mol L -1 for KCl under these applied voltages.

  11. Scaling of C{sub 60} ionization and fragmentation with the energy deposited in collisions with H{sup +}, H{sub 2}{sup +}, H{sub 3}{sup +} and He{sup +} ions (2-130 keV)

    Energy Technology Data Exchange (ETDEWEB)

    Bordenave-Montesquieu, D. [LCAR, IRSAMC, UMR 5589 CNRS, Universite Paul Sabatier, Toulouse (France)]. E-mail: dbm@yosemite.ups-tlse.fr; Moretto-Capelle, P.; Bordenave-Montesquieu, A.; Rentenier, A. [LCAR, IRSAMC, UMR 5589 CNRS, Universite Paul Sabatier, Toulouse (France)

    2001-03-14

    Fragmentation, ionization and C{sub 2} fragment evaporation of the C{sub 60} molecule induced by collisions with H{sup +}, H{sub 2}{sup +}, H{sub 3}{sup +} and He{sup +} monocharged ions have been measured in coincidence with the electron emission in the 2-130 keV projectile energy range. The time-of-flight mass spectra were found to vary strongly with the collision energy or velocity and the projectile. On the other hand, they scale rather nicely with the energy deposited in the molecule. Relative weights of the total multi-fragmentation into small C{sub n}{sup +} fragments (n=1-14), individual multi-fragmentation (n=1,7 and 11), double ionization of the intact molecule and evaporation of C{sub 2} molecules associated with the doubly charged fullerene ion, are used to illustrate our finding quantitatively. (author). Letter-to-the-editor.

  12. Effects of SM-20550, a selective Na+-H+ exchange inhibitor, on the ion transport of myocardial mitochondria.

    Science.gov (United States)

    Hotta, Y; Ishikawa, N; Ohashi, N; Matsui, K

    2001-03-01

    The effect of a novel Na+-H+ exchange inhibitor, SM-20550 [N-(aminoiminomethyl)-1,4-dimethyl-1H-indole-2-carboxamide methanesulfonate] (SM) on the ion transport of myocardial mitochondria was studied using ion fluorometry and superfusion techniques. Isolated mitochondria from the guinea-pig heart were pre-loaded with fluoroprobes of either BCECF AM for H+, SBFI AM for Na+ or fura-2 AM for Ca2+. Initially, the treated mitochondria were superfused with a normal medium (MOPS-buffer, pH 7.4, 24 degrees C), subsequently fluorometric experiments on the Na+, H+, Ca2+ mobilization across the mitochondrial membrane were performed. The intramitochondrial pH (pHm) was increased by the superfusion of Na+ at physiological cytosolic concentrations of 10 mM, indicating the existence of a Na+-H+ exchange in mitochondrial membranes. The Na+ induced elevation of pH was dose-dependently inhibited by SM 1 microM (delta pHm; 45% as drug-free 100%), and 10 microM (delta pHm; 70%), as observed in our experiments with the myocardial sarcolemmal membrane. The selective Na+-H+ exchange inhibitor SM reduced such pHm elevations more markedly than that of EIPA [5-(N-ethyl-N-isopropyl) amiloride]. The Na+-H+ exchange inhibitors, SM and EIPA suppressed the intramitochondrial Ca2+ elevation ([Ca2+]m) brought on by external Ca2+ concentration changes: The pretreatment with SM 1 microM, 10 microM and EIPA 10 microM reduced the [Ca2+]m influx by 28.3, 56.5 and 63%, respectively. Additionally, the [Ca2+]m elevation induced by acidification of the perfusate was reduced by the prior infusion of SM and EIPA. Pretreatment of mitochondria with SM or EIPA which had beneficial effects on the left ventricular developed pressure (LVDP) in the ischemia-reperfusion injury of Langendorff hearts, reduced the intramitochondrial Na+ and pHm levels, indicating interplay of the inhibitory mechanism of Ca2+-uptake into mitochondria coupled with Na+-H+ exchange. These findings suggested that protective effects of Na+-H

  13. Effect of Exposed Surface Area, Volume and Environmental pH on the Calcium Ion Release of Three Commercially Available Tricalcium Silicate Based Dental Cements

    Directory of Open Access Journals (Sweden)

    Sivaprakash Rajasekharan

    2018-01-01

    Full Text Available Tricalcium silicate cements (TSC are used in dental traumatology and endodontics for their bioactivity which is mostly attributed to formation of calcium hydroxide during TSC hydration and its subsequent release of calcium and hydroxide ions. The aim of this study was to determine the effect of volume (Vol, exposed surface area (ESA and pH of surrounding medium on calcium ion release. Three commercially available hydraulic alkaline dental cements were mixed and condensed into cylindrical tubes of varying length and diameter (n = 6/group. For the effect of ESA and Vol, tubes were immersed in 10 mL of deionized water. To analyze the effect of environmental pH, the tubes were randomly immersed in 10 mL of buffer solutions with varying pH (10.4, 7.4 or 4.4. The solutions were collected and renewed at various time intervals. pH and/or calcium ion release was measured using a pH glass electrode and atomic absorption spectrophotometer respectively. The change of pH, short-term calcium ion release and rate at which calcium ion release reaches maximum were dependent on ESA (p < 0.05 while maximum calcium ion release was dependent on Vol of TSC (p < 0.05. Maximum calcium ion release was significantly higher in acidic solution followed by neutral and alkaline solution (p < 0.05.

  14. Effect of Exposed Surface Area, Volume and Environmental pH on the Calcium Ion Release of Three Commercially Available Tricalcium Silicate Based Dental Cements.

    Science.gov (United States)

    Rajasekharan, Sivaprakash; Vercruysse, Chris; Martens, Luc; Verbeeck, Ronald

    2018-01-13

    Tricalcium silicate cements (TSC) are used in dental traumatology and endodontics for their bioactivity which is mostly attributed to formation of calcium hydroxide during TSC hydration and its subsequent release of calcium and hydroxide ions. The aim of this study was to determine the effect of volume (Vol), exposed surface area (ESA) and pH of surrounding medium on calcium ion release. Three commercially available hydraulic alkaline dental cements were mixed and condensed into cylindrical tubes of varying length and diameter ( n = 6/group). For the effect of ESA and Vol, tubes were immersed in 10 mL of deionized water. To analyze the effect of environmental pH, the tubes were randomly immersed in 10 mL of buffer solutions with varying pH (10.4, 7.4 or 4.4). The solutions were collected and renewed at various time intervals. pH and/or calcium ion release was measured using a pH glass electrode and atomic absorption spectrophotometer respectively. The change of pH, short-term calcium ion release and rate at which calcium ion release reaches maximum were dependent on ESA ( p < 0.05) while maximum calcium ion release was dependent on Vol of TSC ( p < 0.05). Maximum calcium ion release was significantly higher in acidic solution followed by neutral and alkaline solution ( p < 0.05).

  15. Quantum infinite order sudden approximation for ion-molecule reactions: treatment of the He + H2+ system

    International Nuclear Information System (INIS)

    Baer, M.; Nakamura, H.; Kouri, D.J.

    1986-01-01

    In this work the ion-molecule reaction He + H 2 + (v/sub i/) → HeH + (v/sub f/) + H(v/sub i/ = 0-7, v/sub f/ = 0-2) was studied quantum mechanically in the energy range 1.3 eV ≤ E/sub tot/ ≤ 1.8 eV. The calculations were carried out employing the Reactive Infinite Order Sudden Approximation (RIOSA). The two features characteristic of this system in the above energy range, namely the strong enhancement of the reaction rate with the initial vibrational energy (at a fixed total energy) and the relatively weak dependence of the cross sections on translational energy, were found to be well reproduced in the numerical treatment. The results also revealed the existence of two mechanisms of the exchange process: one is the ordinary mechanism and the other is probably related to the spectator stripping model

  16. Design of a compact, permanent magnet electron cyclotron resonance ion source for proton and H2+ beam production

    Science.gov (United States)

    Jia, Xianlu; Zhang, Tianjue; Luo, Shan; Wang, Chuan; Zheng, Xia; Yin, Zhiguo; Zhong, Junqing; Wu, Longcheng; Qin, Jiuchang

    2010-02-01

    A 2.45 GHz microwave ion source was developed at China Institute of Atomic Energy (CIAE) for proton beam production of over 60 mA [B.-Q. Cui, Y.-W. Bao, L.-Q. Li, W.-S. Jiang, and R.-W. Wang, Proceedings of the High Current Electron Cyclotron Resonance (ECR) Ion Source for Proton Accelerator, APAC-2001, 2001 (unpublished)]. For various proton beam applications, another 2.45 GHz microwave ion source with a compact structure is designed and will be built at CIAE as well for high current proton beam production. It is also considered to be used for the test of H2+ beam, which could be injected into the central region model cyclotron at CIAE, and accelerated to 5 MeV before extraction by stripping. The required ECR magnetic field is supplied by all the permanent magnets rather than electrical solenoids and six poles. The magnetic field distribution provided by this permanent magnets configuration is a large and uniformly volume of ECR zone, with central magnetic field of a magnitude of ˜875 Gs [T. Taylor and J. S. C. Wills, Nucl. Instrum. Methods Phys. Res. A 309, 37 (1991)]. The field adjustment at the extraction end can be implemented by moving the position of the magnet blocks. The results of plasma, coupling with 2.45 GHz microwave in the ECR zone inside the ion source are simulated by particle-in-cell code to optimize the density by adjusting the magnetic field distribution. The design configuration of the ion source will be summarized in the paper.

  17. Dose dependence of nano-hardness of 6H-SiC crystal under irradiation with inert gas ions

    Science.gov (United States)

    Yang, Yitao; Zhang, Chonghong; Su, Changhao; Ding, Zhaonan; Song, Yin

    2018-05-01

    Single crystal 6H-SiC was irradiated by inert gas ions (He, Ne, Kr and Xe ions) to various damage levels at room temperature. Nano-indentation test was performed to investigate the hardness change behavior with damage. The depth profile of nano-hardness for 6H-SiC decreased with increasing depth for both the pristine and irradiated samples, which was known as indentation size effect (ISE). Nix-Gao model was proposed to determine an asymptotic value of nano-hardness by taking account of ISE for both the pristine and irradiated samples. In this study, nano-hardness of the irradiated samples showed a strong dependence on damage level and showed a weak dependence on ions species. From the dependence of hardness on damage, it was found that the change of hardness demonstrated three distinguishable stages with damage: (I) The hardness increased with damage from 0 to 0.2 dpa and achieved a maximum of hardening fraction ∼20% at 0.2 dpa. The increase of hardness in this damage range was contributed to defects produced by ion irradiation, which can be described well by Taylor relation. (II) The hardness reduced rapidly with large decrement in the damage range from 0.2 to 0.5 dpa, which was considered to be from the covalent bond breaking. (III) The hardness reduced with small decrement in the damage range from 0.5 to 2.2 dpa, which was induced by extension of the amorphous layer around damage peak.

  18. High-intensity ion sources for accelerators with emphasis on H- beam formation and transport (invited)

    International Nuclear Information System (INIS)

    Keller, R.

    2010-01-01

    This paper lays out the fundamental working principles of a variety of high-current ion sources for accelerators in a tutorial manner, and gives examples of specific source types such as dc discharge-driven and rf-driven multicusp sources, Penning-type, and electron cyclotron resonance-based sources while discussing those principles, pointing out general performance limits as well as the performance parameters of specific sources. Laser-based, two-chamber, and surface-ionization sources are briefly mentioned. Main aspects of this review are particle feed, ionization mechanism, beam formation, and beam transport. Issues seen with beam formation and low-energy transport of negative hydrogen-ion beams are treated in detail.

  19. Electron interference in fast ion collisions with H2 and the frequency parameter

    Science.gov (United States)

    Chatterjee, S.; Misra, D.; Fainstein, P. D.; Tribedi, L. C.

    2011-06-01

    The Young-type interference effect has been investigated in electron emission from molecular hydrogen in collision of 5 MeV u- 1 F9+ ions. The double differential cross section ratios of molecular-to-atomic hydrogen exhibits oscillatory structure, which is discussed in terms of the Young-type electron interference. We have obtained the frequencies of such oscillation for different angles. A comparative study of the frequency parameter is given with early measurements performed by other groups.

  20. A study of effective atomic numbers and electron densities of some vitamins for electron, H, He and C ion interactions

    Science.gov (United States)

    Büyükyıldız, M.

    2017-09-01

    The radiological properties of some vitamins such as Retinol, Beta-carotene, Riboflavin, Niacin, Niacinamide, Pantothenic acid, Pyridoxine, Pyridoxamine, Pyridoxal, Biotin, Folic acid, Ascorbic acid, Cholecalciferol, Alpha-tocopherol, Gamma-tocopherol, Phylloquinone have been investigated with respect to total electron interaction and some heavy charged particle interaction as means of effective atomic numbers (Z_{eff}) and electron densities (N_{eff}) for the first time. Calculations were performed for total electron interaction and heavy ions such as H, He and C ion interactions in the energy region 10keV-10MeV by using a logarithmic interpolation method. Variations in Z_{eff}'s and N_{eff}'s of given vitamins have been studied according to the energy of electron or heavy charged particles, and significant variations have been observed for all types of interaction in the given energy region. The maximum values of Z_{eff} have been found in the different energy regions for different interactions remarkably and variations in N_{eff} seem approximately to be the same with variation in Z_{eff} for the given vitamins as expected. Z_{eff} values of some vitamins were plotted together and compared with each other for electron, H, He and C interactions and the ratios of Z_{eff}/ have been changed in the range of 0.25-0.36, 0.20-0.36, 0.22-0.35 and 0.20-0.35 for electron, H, He and C interactions, respectively.

  1. Temperature Dependence of Disorder Accumulation and Amorphization in Au-Ion Irradiated 6H-SiC

    International Nuclear Information System (INIS)

    Jiang, Weilin; Zhang, Yanwen; Weber, William J.

    2004-01-01

    Disorder accumulation and amorphization in 6H-SiC single crystals irradiated with 2.0 MeV Au 2+ ions at temperatures ranging from 150 to 550 K have been investigated systematically based on 0.94 MeV D + channeling analyses along the axis. Physical models have been applied to fit the experimental data and to interpret the temperature dependence of the disordering processes. Results show that defect-stimulated amorphization in Au 2+ -irradiated 6H-SiC dominates the disordering processes at temperatures below 500 K, while formation of clusters becomes predominant above 500 K. Two distinctive dynamic recovery stages are observed over the temperature range from 150 to 550 K, resulting from the coupled processes of close-pair recombination and interstitial migration and annihilation on both sublattices. These two stages overlap very well with the previously observed thermal recovery stages. Based on the model fits, the critical temperature for amorphization in 6H-SiC under the Au 2+ ion irradiation conditions corresponds to 501 ± 10 K

  2. Application of NIR - CRDS for state selective study of recombination of para and ortho H3+ ions with electrons in low temperature plasma

    Science.gov (United States)

    Varju, J.; Roučka, Š.; Kotrík, T.; Plašil, R.; Glosík, J.

    2010-05-01

    We present a study of H3+ recombination performed at 77 K on the two lowest rotational levels of this ion, which belong to its two different nuclear spin states of the studied ion. A near infrared cavity ring-down spectrometer (~1381 nm, CRDS arrangement) has been used to obtain the time evolution of concentration of both states. From the overall ion density decay during the afterglow we obtained the binary recombination rate coefficient αbin (77 K) = 1.2×10-7 cm3s-1. We have also observed ternary helium assisted recombination of both para and ortho H3+. The process is very slow (at 77 K) and the obtained ternary recombination rate coefficient is in contradiction with the theoretical prediction. It is the first time that the binary and ternary H3+ recombination rate coefficient was measured at a known population of para and ortho H3+ ions in decaying plasma.

  3. Application of NIR - CRDS for state selective study of recombination of para and ortho H3+ ions with electrons in low temperature plasma

    International Nuclear Information System (INIS)

    Varju, J; Roucka, S; KotrIk, T; Plasil, R; Glosik, J

    2010-01-01

    We present a study of H 3 + recombination performed at 77 K on the two lowest rotational levels of this ion, which belong to its two different nuclear spin states of the studied ion. A near infrared cavity ring-down spectrometer (∼1381 nm, CRDS arrangement) has been used to obtain the time evolution of concentration of both states. From the overall ion density decay during the afterglow we obtained the binary recombination rate coefficient α bin (77 K) = 1.2x10 -7 cm 3 s -1 . We have also observed ternary helium assisted recombination of both para and ortho H 3 + . The process is very slow (at 77 K) and the obtained ternary recombination rate coefficient is in contradiction with the theoretical prediction. It is the first time that the binary and ternary H 3 + recombination rate coefficient was measured at a known population of para and ortho H 3 + ions in decaying plasma.

  4. Forward backward asymmetry in electron emission from H{sub 2}by fast carbon ions and Young type interference effect

    Energy Technology Data Exchange (ETDEWEB)

    Misra, D [Tata Institute of Fundamental Research, H. B. Road, Colaba, Mumbai-400005 (India); Kelkar, A H [Tata Institute of Fundamental Research, H. B. Road, Colaba, Mumbai-400005 (India); Kadhane, U [Tata Institute of Fundamental Research, H. B. Road, Colaba, Mumbai-400005 (India); Kumar, A; Fainstein, Pd [Centro Atomico Bariloche, 8400 Bariloche (Argentina); Tribedi, L C [Tata Institute of Fundamental Research, H. B. Road, Colaba, Mumbai-400005 (India)

    2007-03-01

    We have investigated the effect of Young type interference on the forward backward angular asymmetry in electron emission from molecular hydrogen in collisions with fast bare carbon ions. The asymmetry parameter shows an oscillatory behaviour as a function of electron velocity which is absent in atomic target such as He. It is shown that the asymmetry parameter which is based on DDCS from H{sub 2}only can be a tool to investigate the Young type interference. The measured energy and angular distributions as well as the asymmetry parameter are compared with a molecular CDW-EIS (continuum distorted wave-eikonal initial state) model.

  5. Study of ion viscosity by spontaneous L-H transitions under marginal hot cathode biasing in the Tohoku University Heliac

    International Nuclear Information System (INIS)

    Kitajima, S.; Takahashi, H.; Tanaka, Y.; Utoh, H.; Takenaga, M.; Yokoyama, M.; Inagaki, S.; Suzuki, Y.; Nishimura, K.; Ogawa, H.; Takayama, M.; Shinde, J.; Ogawa, M.; Aoyama, H.; Iwazaki, K.; Okamoto, A.; Shinto, K.; Sasao, M.

    2008-01-01

    Using the spontaneous transition condition under marginal hot cathode biasing, the ion viscosity at the L-H transition was estimated in various magnetic configurations in the Tohoku University Heliac. The critical viscosity, which is the viscosity at the transition point, was experimentally estimated from the J x B driving force. The critical viscosities in different magnetic configurations were in agreement with the neoclassical predictions within a factor of 2 and were compared with the viscosities obtained in the externally forced biasing experiments. Although the transition points were spread over a wide range, poloidal Mach numbers at the transition point were concentrated near the viscosity maxima predicted by the theory

  6. Elastic forward analysis using sup 7 Li ions A useful tool for H and light elements determination

    CERN Document Server

    Romero, S; Murillo, G; Berdejo, H M

    2002-01-01

    Films of CN sub x /Si, TiN sub x /AISI 304 and AlO sub x /Si were analyzed with sup 7 Li ions from 4.0 to 4.5 MeV and an experimental arrangement that, through detection of scattered projectiles and recoils by a single detector, allows quantification of H, light elements and heavier ones. A discussion is presented of the capabilities of Rutherford backscattering spectrometry (RBS) and conventional elastic recoil detection analysis (ERDA) compared to elastic forward analysis.

  7. Application of linear pH gradients for the modeling of ion exchange chromatography: Separation of monoclonal antibody monomer from aggregates.

    Science.gov (United States)

    Kluters, Simon; Wittkopp, Felix; Jöhnck, Matthias; Frech, Christian

    2016-02-01

    The mobile phase pH is a key parameter of every ion exchange chromatography process. However, mechanistic insights into the pH influence on the ion exchange chromatography equilibrium are rare. This work describes a mechanistic model capturing salt and pH influence in ion exchange chromatography. The pH dependence of the characteristic protein charge and the equilibrium constant is introduced to the steric mass action model based on a protein net charge model considering the number of amino acids interacting with the stationary phase. This allows the description of the adsorption equilibrium of the chromatographed proteins as a function of pH. The model parameters were determined for a monoclonal antibody monomer, dimer, and a higher aggregated species based on a manageable set of pH gradient experiments. Without further modification of the model parameters the transfer to salt gradient elution at fixed pH is demonstrated. A lumped rate model was used to predict the separation of the monoclonal antibody monomer/aggregate mixture in pH gradient elution and for a pH step elution procedure-also at increased protein loadings up to 48 g/L packed resin. The presented model combines both salt and pH influence and may be useful for the development and deeper understanding of an ion exchange chromatography separation. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. Effect of H{sup +} ion implantation on structural, morphological, optical and dielectric properties of L-arginine monohydrochloride monohydrate single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Sangeetha, K. [Crystal Growth and Thin film Laboratory, Department of Physics, School of Physics, Bharathidasan University, Tiruchirappalli 620024, Tamil Nadu (India); Babu, R. Ramesh, E-mail: rampap2k@yahoo.co.in [Crystal Growth and Thin film Laboratory, Department of Physics, School of Physics, Bharathidasan University, Tiruchirappalli 620024, Tamil Nadu (India); Kumar, P. [Inter-University Accelerator Centre, P.O. Box 10502, Aruna Asaf Ali Marg, New Delhi 110067 (India); Bhagvannarayana, G. [Materials Characterization Division, National Physical Laboratory, New Delhi 110012 (India); Ramamurthi, K. [Crystal Growth and Thin film Laboratory, Department of Physics, School of Physics, Bharathidasan University, Tiruchirappalli 620024, Tamil Nadu (India)

    2011-06-15

    L-arginine monohydrochloride monohydrate (LAHCl) single crystals have been implanted with 100 keV H{sup +} ions at different ion fluence ranging from 10{sup 12} to 10{sup 15} ions/cm{sup 2}. Implanted LAHCl single crystals have been investigated for property changes. Crystal surface and crystalline perfection of the pristine and implanted crystals were analyzed by atomic force microscope and high-resolution X-ray diffraction studies, respectively. Optical absorption bands induced by colour centers, refractive index and birefringence, mechanical stability and dielectric constant of implanted crystals were studied at different ion fluence and compared with that of pristine LAHCl single crystal.

  9. Investigation of instability of M23C6 particles in F82H steel under electron and ion irradiation conditions

    Science.gov (United States)

    Kano, Sho; Yang, Huilong; Shen, Jingjie; Zhao, Zishou; McGrady, John; Hamaguchi, Dai; Ando, Mamami; Tanigawa, Hiroyasu; Abe, Hiroaki

    2018-04-01

    In order to clarify the instability of M23C6 in F82H steel under irradiation, both electron irradiation using a high voltage electron microscope (HVEM) and ion irradiation using an ion accelerator were performed. For the electron irradiation, in-situ observation under 2 MV electron irradiation and ex-situ high resolution electron microscopic (HREM) analysis were utilized to evaluate the response of M23C6 against irradiation. The temperature dependence of the irradiation induced instability of the carbide was first confirmed: 293 K TEM specimens were prepared by a focused ion beam technique. The shrinkage of carbide particles was observed especially near the irradiation surface. Besides, the lattice fringes at the periphery of carbide were observed in the irradiated M23C6 by the HREM analysis, which is different from that observed in the electron irradiation. It was clarified that the instability of M23C6 is dependent on the irradiation conditions, indicating that the flow rate of vacancy type defects might be the key factor to cause the dissolution of constituent atoms of carbide particles into matrix under irradiation.

  10. Experiments with planar inductive ion source meant for creation ofH+ Beams

    Energy Technology Data Exchange (ETDEWEB)

    Vainionpaa, J.H.; Kalvas, T.; Hahto, S.K.; Reijonen, J.

    2007-02-07

    In this article the effect of different engineering parameters of an rf-driven ion sources with external spiral antenna and quartz disk rf-window are studied. Paper consists of three main topics: The effect of source geometry on the operation gas pressure, the effect of source materials and magnetic confinement on extracted current density and ion species and the effect of different antenna geometries on the extracted current density. The operation gas pressure as a function of the plasma chamber diameter, was studied. This was done with three cylindrical plasma chambers with different inner diameters. The chamber materials were studied using two materials, aluminum and alumina (AlO{sub 2}). The removable 14 magnet multicusp confinement arrangement enabled us to compare the effects of the two wall materials with and without the magnetic confinement. Highest proton fraction of {approx} 8% at 2000 W of rf-power and at pressure of 1.3 Pa was measured using AlO{sub 2} plasma chamber and no multicusp confinement. For all the compared ion sources at 1000W of rf-power, source with multicusp confinement and AlO2 plasma chamber yields highest current density of 82.7 mA/cm{sup 2} at operation pressure of 4 Pa. From the same source highest measured current density of 143 mA/cm{sup 2} at 1.3 Pa and 2200W of rf-power was achieved. Multicusp confinement increased the maximum extracted current up to factor of two. Plasma production with different antenna geometries was also studied. Antenna tests were performed using same source geometry as in source material study with AlO{sub 2} plasma chamber and multicusp confinement. The highest current density was achieved with 4.5 loop solenoid antenna with 6 cm diameter. Slightly lower current density with lower pressure was achieved using tightly wound 3 loop spiral antenna with 3.3 cm ID and 6 cm OD.

  11. Electron interference in fast ion collisions with H{sub 2} and the frequency parameter

    Energy Technology Data Exchange (ETDEWEB)

    Chatterjee, S; Misra, D; Tribedi, L C [Tata Institute of Fundamental Research, Homi Bhabha Road, Colaba, Mumbai 400 005 (India); Fainstein, P D, E-mail: lokesh@tifr.res.in [Centro Atomico Bariloche, 8400 Bariloche (Argentina)

    2011-06-15

    The Young-type interference effect has been investigated in electron emission from molecular hydrogen in collision of 5 MeV u{sup -1} F{sup 9+} ions. The double differential cross section ratios of molecular-to-atomic hydrogen exhibits oscillatory structure, which is discussed in terms of the Young-type electron interference. We have obtained the frequencies of such oscillation for different angles. A comparative study of the frequency parameter is given with early measurements performed by other groups.

  12. Cation mobility and kinetics of ion exchange in zirconium hydrogen monothiophosphate hydrate, Zr(HPO(3)S)(2)x1.5H(2)O.

    Science.gov (United States)

    Stenina, I A; Aliev, A D; Dorhout, P K; Yaroslavtsev, A B

    2004-11-01

    The ion conductivity of zirconium hydrogen monothiophosphate (Zr(HPO(3)S)(2)x1.5H(2)O) has been measured by impedance spectroscopy. The measured value of proton conductivity is 3 x 10(-5) S/cm at 298 K. Conductivity was shown to decrease with increasing temperature due to a dehydration process. Above 450 K, the conductivity is likely governed by proton transport in the anhydrous phase Zr(HPO(3)S)(2). The activation energies of proton conductivity were measured to be 18 +/- 2 kJ/mol for Zr(HPO(3)S)(2)x1.5H(2)O and 60 +/- 3 kJ/mol for the anhydrous compound. The kinetics of ion exchange was studied with the use of potentiometric titration for several ion pairs, H(+)/Na(+), H(+)/Zn(2+), and Na(+)/Zn(2+) in Zr(HPO(3)S)(2)x1.5H(2)O. The diffusion coefficient values for H(+)/Na(+) ion exchange in Zr(HPO(3)S)(2)x1.5H(2)O are lower than those reported in alpha-zirconium phosphate. At the same time, the mobility of zinc ions in Zr(HPO(3)S)(2)x1.5H(2)O is higher than sodium ion mobility. The ion exchange H(+)/Zn(2+) is accompanied by the slow hydrolysis of the initial compound. In all cases, the powdered solids were evaluated by powder X-ray diffraction, and particle sizes were controlled by grinding and sieving the powders.

  13. Evaluation of radiopacity, pH, release of calcium ions, and flow of a bioceramic root canal sealer.

    Science.gov (United States)

    Candeiro, George Táccio de Miranda; Correia, Fabrícia Campelo; Duarte, Marco Antônio Húngaro; Ribeiro-Siqueira, Danieli Colaço; Gavini, Giulio

    2012-06-01

    The aim of the present study was to evaluate the physicochemical properties of a bioceramic root canal sealer, Endosequence BC Sealer. Radiopacity, pH, release of calcium ions (Ca(2+)), and flow were analyzed, and the results were compared with AH Plus cement. Radiopacity and flow were evaluated according to ISO 6876/2001 standards. For the radiopacity analysis, metallic rings with 10-mm diameter and 1-mm thickness were filled with cements. The radiopacity value was determined according to radiographic density (mm Al). The flow test was performed with 0.05 mL of cement placed on a glass plate. A 120-g weight was carefully placed over the cement. The largest and smallest diameters of the disks formed were measured by using a digital caliper. The release of Ca(2+) and pH were measured at periods of 3, 24, 72, 168, and 240 hours with spectrophotometer and pH meter, respectively. Data were analyzed by analysis of variance and Tukey test (P pH analysis showed that Endosequence BC Sealer showed pH and release of Ca(2+) greater than those of AH Plus (P root canal sealer. Copyright © 2012 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  14. Loss of CO/+/ ions by reaction with H2 in OMC-1

    Science.gov (United States)

    Huntress, W. T., Jr.; Prasad, S. S.; Kemper, P. R.; Cates, R. D.; Bowers, M. T.

    1982-01-01

    The temperature dependence of the rate constant for the reaction CO(+)+H2 yields HCO(+) has been measured in the temperature range 100-390 K. The rate constant has no dependence on temperature in this range, indicating that at the temperatures prevalent in OMC-1, the rate of loss of CO(+) by reaction with H2 is much too large to allow for the observed column abundance under steady-state conditions.

  15. The role of calcium ions in the photocatalytic oxidation of humic acid at neutral pH.

    Science.gov (United States)

    Mariquit, Eden G; Salim, Chris; Hinode, Hirofumi

    2008-10-01

    Humic acids (HAs) are natural organic matter derived from the decomposition of plant, algal, and microbial materials. They belong to the group of the most predominant type of natural organic matter present in ground and surface waters. HAs affect the mobility and bioavailability of aquatic contaminants. However, if they are left unremoved from the water before water treatment processes, they can form carcinogenic disinfection by-products, such as trihalomethanes, haloacetic acids, and other halogenated disinfection by-products, that can pose a threat to human beings. An advanced oxidation process using UV light and a commercially available titanium dioxide was used to oxidize HA at a pH that is similar to that of natural water. The effect of adding calcium ions to the adsorption and the photocatalytic oxidation of HAs was studied. The effect of varying the TiO(2) load was also investigated. The experiment was done using a photochemical batch reactor equipped with a mercury lamp emitting light with wavelengths of 310-580 nm. The absorbances by the samples were determined at wavelengths of 254 nm and 436 nm, which represent the aromatic-compound content of and the color of the solution, respectively. Results indicated calcium ions have an effect on both the adsorption and the photocatalytic oxidation of HA at a pH within 8.0 +/- 0.5. Calcium ions facilitated adsorption of HA onto the surface of TiO(2) and resulted to faster photocatalytic oxidation. The data were plotted with respect to the normalized absorbances and irradiation time.

  16. Emittance measurements for optimum operation of the J-PARC RF-driven H{sup −} ion source

    Energy Technology Data Exchange (ETDEWEB)

    Ueno, A., E-mail: akira.ueno@j-parc.jp; Ohkoshi, K.; Ikegami, K.; Takagi, A.; Yamazaki, S.; Oguri, H. [J-PARC Center, Tokai-mura, Naka-gun, Ibaraki-ken 319-1195 (Japan)

    2015-04-08

    In order to satisfy the Japan Proton Accelerator Research Complex (J-PARC) second stage requirements of an H{sup −} ion beam of 60mA within normalized emittances of 1.5πmm•mrad both horizontally and vertically, a flat top beam duty factor of 1.25% (500μs×25Hz) and a life-time of longer than 1month, the J-PARC cesiated RF-driven H{sup −} ion source was developed by using an internal-antenna developed at the Spallation Neutron Source (SNS). The transverse emittances of the source were measured with various conditions to find out the optimum operation conditions minimizing the horizontal and vertical rms normalized emittances. The transverse emittances were most effectively reduced by operating the source with the plasma electrode temperature lower than 70°C. The optimum value of the cesium (Cs) density around the beam hole of the plasma electrode seems to be proportional to the plasma electrode temperature. The fine control of the Cs density is indispensable, since the emittances seem to increase proportionally to the excessiveness of the Cs density. Furthermore, the source should be operated with the Cs density beyond a threshold value, since the plasma meniscus shape and the ellipse parameters of the transverse emittances seem to be changed step-function-likely on the threshold Cs value.

  17. Collision-Induced Dissociation of Fatty Acid [M - 2H + Na]- Ions: Charge-Directed Fragmentation and Assignment of Double Bond Position

    Science.gov (United States)

    Thomas, Michael C.; Altvater, Jens; Gallagher, Thomas J.; Nette, Geoffrey W.

    2014-08-01

    The collision-induced dissociation (CID) of cationic fatty acid-metal ion complexes has been extensively studied and, in general, provides rich structural information. In particular, charge-remote fragmentation processes are commonly observed allowing the assignment of double bond position. In a previous manuscript, we presented two methods to doubly deprotonate polyunsaturated fatty acids to form anionic fatty acid-sodium ion complexes, referred to as [M - 2H + Na] - ions. In the current manuscript, the CID behavior of these [M - 2H + Na] - ions is investigated for the first time. Significantly, we also present a deuterium-labeling experiment, which excludes the possibility that deprotonation occurs predominately at the α-carbon in the formation of fatty acid [M - H + NaF]- ions. This supports our original proposal where deprotonation occurs at the bis-allylic positions of polyunsaturated fatty acids. CID spectra of polyunsaturated fatty acid [M - 2H + Na]- ions display abundant product ions arising from acyl chain cleavages. Through the examination of fatty acid isomers, it is demonstrated that double bond position may be unequivocally determined for methylene-interrupted polyunsaturated fatty acids with three or more carbon-carbon double bonds. In addition, CID of [M - 2H + Na]- ions was applied to 18:3 isomers of Nannochloropsis oculata and three isomers were tentatively identified: Δ9,12,1518:3, Δ6,9,1218:3, and Δ5,8,1118:3. We propose that structurally-informative product ions are formed via charge-driven fragmentation processes at the site of the resonance-stabilized carbanion as opposed to charge-remote fragmentation processes, which could be inferred if deprotonation occurred predominately at the α-carbon.

  18. Ion-pair extraction of [3H]stobadine from biological fluids

    International Nuclear Information System (INIS)

    Scasnar, V.

    1998-01-01

    A simple and specific radiometric assay was developed for the determination of stobadine, a cardioprotective drug, in the serum of experimental animals. The assay is based on a single extraction step of the radioactively labeled drug from serum into the benzene solution of dicarbolide of cobalt followed by quantitation of the extracted radioactivity by using liquid scintillation counting. The extraction mechanism involves the ion-pair formation between the protonized molecule of stobadine and the hydrophobic, negatively charged molecule of dicarbolide of cobalt. The extraction yield of stobadine from 1 ml of serum was 95% in the concentration range from 1 to 6000 ng/ml. The co-extraction of metabolites was less than 5%. The method was applied to the determination of stobadine in serum of dogs and the data obtained were in a good agreement with those obtained by high performance liquid chromatography. (author)

  19. Experimental studies of the formation of cluster ions formed by corona discharge in an atmosphere containing SO2, NH3, and H2O

    DEFF Research Database (Denmark)

    Hvelplund, Preben; Pedersen, Jens Olaf Pepke; Støchkel, Kristian

    2013-01-01

    Abstract We report on studies of ion-induced nucleation in a corona discharge taking place in an atmosphere containing SO2, NH3, and H2O at standard temperature and pressure. Positive ions such as H3O+(H2O)n, NH4+(H2O)n, and H+(H2SO4)(H2O)n and negative ions such as HSO5-(H2O)n, SO4-(H2O)n, HSO4-(H......5-, which has been observed in many studies, in our experiments is contaminated by O2-(HNO3)(H2O) ions, and this may also have been the case in other experiments. Finally an ion with m/z = 232 (where m is the cluster mass in amu and z is the charge state), capable of attaching H2O...

  20. Ab initio investigation of electron capture by Cl7+ ions from H

    International Nuclear Information System (INIS)

    Zhao, L. B.; Stancil, P. C.; Watanabe, A.; Kimura, M.

    2007-01-01

    An investigation of charge transfer in collisions of ground-state Cl 7+ with H has been conducted based on a fully quantum-mechanical molecular-orbital close-coupling (QMOCC) approach. The charge-transfer process Cl 7+ ( 1 S)+H→Cl 6+ (2p 6 nl 2 S, 2 P o , 2 D, 2 F o , 2 G)+H + with n=5 and 6 is taken into account for collision energies between 10 -4 eV/u and 1 keV/u. The relevant adiabatic potentials and nonadiabatic coupling matrix elements for the ClH 7+ system are evaluated with the configuration-interaction method. The investigation shows that electron capture into the 5d, 5f, 5g, and 6p states dominates for collision energies less than ∼1 eV/u, while above 100 eV/u the 5s, 5p, 5d, and 6p are the primary capture channels. Comparison with experimental data for collisions of Cl 7+ ( 1 S) with D reveals a discrepancy over the full range of measured energies (5-430 eV/u), while no significant isotope effect is found for QMOCC calculations with deuterium. Furthermore, comparison with a previous calculation of the one-electron N 7+ +H system, as well as measurements of the multielectron Al 7+ +H and Fe 7+ +H systems, suggests that the electronic structure of the core has a non-negligible effect on the charge-transfer process. A one-electron model for relative l distributions is found to agree with the QMOCC results for n=5 between 100 and 1000 eV/u, but fails at lower collision energies. Finally, state-selective and total rate coefficients are given for temperatures between 10 and 200 000 K

  1. pH, calcium ion release, and setting time of an experimental mineral trioxide aggregate-based root canal sealer.

    Science.gov (United States)

    Massi, Santiago; Tanomaru-Filho, Mário; Silva, Guilherme Ferreira; Duarte, Marco Antonio Hungaro; Grizzo, Larissa Tercilia; Buzalaf, Marília Afonso Rabelo; Guerreiro-Tanomaru, Juliane Maria

    2011-06-01

    An experimental mineral trioxide aggregate sealer (MTAS) has been developed for use as a root canal sealer. The aim of this study was to evaluate the setting time, pH, and calcium ion release of MTAS compared with white Portland cement (CPB-40; Votorantin Cimentos, Camargo Correa SA, Pedro Leopoldo, MG, Brazil), white MTA Angelus (MTA; Angelus, Londrina, PR, Brazil), and AH Plus (Dentsply DeTrey, Konstanz, Germany). For the evaluation of setting time, each material was analyzed using Gilmore-type needles. Polyethylene tubes with the materials were immersed in distilled water for the measurement of pH (digital pH meter) and calcium release (atomic absorption spectrophotometry). The evaluations were performed at 3, 6, 12, 24, and 48 hours and 7, 14, and 28 days. Data were analyzed by analysis of variance and the Tukey test at 5% significance level. MTAS showed higher calcium release at all experimental periods, a greater increase in pH up to 48 hours and the longest setting time. MTAS presented favorable properties for its indication as a root canal sealer. Copyright © 2011 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  2. Conformation-Specific Infrared and Ultraviolet Spectroscopy of Cold [YAPAA+H]^{+} and [YGPAA+H]^{+} Ions: a Stereochemical "twist" on the β-HAIRPIN Turn

    Science.gov (United States)

    DeBlase, Andrew F.; Harrilal, Christopher P.; Lawler, John T.; Burke, Nicole L.; McLuckey, Scott A.; Zwier, Timothy S.

    2017-06-01

    Incorporation of the unnatural D-proline (^{D}P) stereoisomer into a polypeptide sequence is a typical strategy to encourage formation of β-hairpin loops because natural sequences are often unstructured in solution. Using conformation-specific IR and UV spectroscopy of cold (10 K) gas-phase ions, we probe the inherent conformational preferences of the ^{D}P and ^{L}P diastereomers in the protonated peptide [YAPAA+H]^{+}, where only intramolecular interactions are possible. Consistent with the solution phase studies, one of the conformers of [YADPAA+H]^{+} is folded into a charge-stabilized β-hairpin turn. However, a second predominant conformer family containing two sequential γ-turns is also identified, with similar energetic stability. A single conformational isomer of the ^{L}P diastereomer, [YALPAA+H]^{+}, is found and assigned to a structure that is not the anticipated "mirror image" β-turn. Instead, the ^{L}P stereo center promotes a cis alanine-proline amide bond. The assigned structures contain clues that the preference of the ^{D}P diastereomer to support a trans-amide bond and the proclivity of ^{L}P for a cis-amide bond is sterically driven and can be reversed by substituting glycine for alanine in position 2, forming [YGLPAA+H]^{+}. These results provide a basis for understanding the residue-specific and stereo-specific alterations in the potential energy surface that underlie these changing preferences, providing insights to the origin of β-hairpin formation.

  3. Tuning the intermolecular proton bond in the H5O2+ `Zundel ion' scaffold

    DEFF Research Database (Denmark)

    Olesen, S. G.; Guasco, T. L.; Roscioli, J. R.

    2011-01-01

    a remarkably similar trend as the exterior OH groups are sequentially solvated or are replaced by methyl substituents. In effect, solvents H-bonding to exterior OH groups act to increase the proton affinity of the water to which they are bound in a roughly additive fashion. We discuss this behavior...

  4. Computation of the H-wave accelerating structure of ion linacs

    International Nuclear Information System (INIS)

    Barsukov, A.B.; Dajkovskij, A.D.; Igoshin, V.B.; Portugalov, Yu.I.; Ryabov, A.D.

    1982-01-01

    The paper describes the method of engeneering computatjon of H-wave acceleratipg strUctures, used for low energy heavy particle accelerators. For this aim the computer code SUPERFISH-1 has been used. The results of theoretical analysis for some cavitjes with longitudinal magnetic field are given as well as comparison between calculated and experimental resulst

  5. Blistering in alloy Ti–6Al–4V from H+ ion implantation

    Indian Academy of Sciences (India)

    Administrator

    nal gas filled bubbles and low pressure of the gas in them. The development of microblisters in the implanted area, resulting from natural ageing at room temperature for a period of nearly five months, prior to annealing at. Figure 5. SEM micrograph showing vein like features (VLF) on macroblister, resulting from 150 keV H.

  6. Classical and semiclassical treatments of highly charged ions + H(1s) collisions

    International Nuclear Information System (INIS)

    Errea, L.F.; Illescas, C.; Mendez, L.; Pons, B.; Riera, A.; Suarez, J.

    2005-01-01

    We present impact-parameter classical trajectory Monte-Carlo and molecular close-coupling calculations for total and partial cross sections for Ne 10+ , Ar 18 + H(1s) collisions, which have recently became of interest in fusion plasma research

  7. Electron capture and ionization in collisions of multiply charged ions with H(2s)

    International Nuclear Information System (INIS)

    Errea, L F; Guzman, F; Illescas, Clara; Mendez, L; Pons, B; Riera, A; Suarez, J

    2007-01-01

    We present total cross sections for electron capture and ionization in collisions of B 5+ and Ne 10+ with H(2s), calculated using two methods: the semiclassical close-coupling molecular formalism and the eikonal-CTMC method. We have evaluated partial cross sections for capture into excited n-levels, required in plasma diagnostics

  8. Electron capture in collisions between O6+ ions and H2O molecules

    NARCIS (Netherlands)

    Bodewits, D.; Hoekstra, R.

    By means of photon emission spectroscopy, state selective electron capture cross section for low energy (0.1-7.5 keV/amu) collisions of O6+ on H2O molecules have been measured. Over the range of interaction energies the state selective cross sections change strongly, i.e., by factors up to 5, while

  9. Recrystallization effects of swift heavy {sup 209}Bi ions irradiation on electrical degradation in 4H-SiC Schottky barrier diode

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Zhimei; Ma, Yao; Gong, Min [Key Laboratory for Microelectronics, College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Key Laboratory of Radiation Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China); Li, Yun [Key Laboratory for Microelectronics, College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Huang, Mingmin [Key Laboratory for Microelectronics, College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Key Laboratory of Radiation Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China); Gao, Bo [Key Laboratory for Microelectronics, College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Zhao, Xin, E-mail: zhaoxin1234@scu.edu.cn [Key Laboratory for Microelectronics, College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China)

    2017-06-15

    In this paper, the phenomenon that the recrystallization effects of swift heavy {sup 209}Bi ions irradiation can partially recovery damage with more than 1 × 10{sup 10} ions/cm{sup 2} is investigated by the degradation of the electrical characteristics of 4H-SiC Schottky barrier diode (SBD) with swift heavy ion irradiation. Deep level transient spectroscopy (DLTS) and Current-Voltage (I-V) measurements clearly indicated that E{sub 0.62} defect induced by swift heavy ion irradiation, which was a recombination center, could result in the increase of reverse leakage current (I{sub R}) at fluence less than 1 × 10{sup 9} ions/cm{sup 2} and the recovery of I{sub R} at fluence more than 1 × 10{sup 10} ions/cm{sup 2} in 4H-SiC SBD. The variation tendency of I{sub R} is consisted with the change of E{sub 0.62} defect. Furthermore, it is reasonable explanation that the damage or defect formed at low fluence in SiC may be recovered by further swift heavy ion irradiation with high fluence, which is due to the melting with the ion tracks of the amorphous zones through a thermal spike and subsequent epitaxial recrystallization initiated from the neighboring crystalline regions.

  10. Uranium Isotopes in Calcium Carbonate: A Possible Proxy for Paleo-pH and Carbonate Ion Concentration?

    Science.gov (United States)

    Chen, X.; Romaniello, S. J.; Herrmann, A. D.; Wasylenki, L. E.; Anbar, A. D.

    2015-12-01

    abiotic CaCO3 reflect changes in aqueous U(VI) speciation, which are in turn a function of carbonate ion chemistry and pH. Hence, the door is opened to the development of a possible 238U/235U proxy for the carbonate ion system. [1] DeCarlo et al., (2015), GCA, 162,151-165. [2] Reeder et a., (2001), GCA, 65, 3491-3503. [3] Weyer et al., (2008) GCA 72, 345-359.

  11. Reactions of POxCly- ions with O2(a 1[Delta]g), H2O, and Cl2 at 298 K

    Science.gov (United States)

    Midey, Anthony J.; Dotan, Itzhak; Viggiano, A. A.

    2008-06-01

    The rate constants and product branching ratios for the reactions of phosphorus oxychloride anions, POxCly- for x = 1-2 and y = 1-3, with O2(a 1[Delta]g), Cl2, and H2O have been measured in a selected ion flow tube (SIFT) at 298 K. A mixture of O2(a 1[Delta]g) in O2 has been produced using a recently designed chemical singlet oxygen generator (sparger) with an emission detection scheme adopted previously in our laboratory. The experiments continue a series of investigations into the oxidation reactions of POxCly- ions, searching for pathways to the terminal PO2- and PO3- ions observed in combustion chemistry with POCl3 present. None of the POxCly- ions react with H2O or O2(a 1[Delta]g). The O2(a 1[Delta]g) rate constants have a limit of <1 × 10-11 cm3 s-1, except for PO2Cl- where a limit of <5 × 10-11 cm3 s-1 has been determined. The H2O rate constants have limits of <1 × 10-11 cm3 s-1. All of the POxCly- ions react with Cl2, excluding PO3- and PO2Cl2-. Depending on the reactant ion, Cl-, Cl2- or PO2Cl2- product ions form.

  12. Manganese ions enhance mitochondrial H2O2emission from Krebs cycle oxidoreductases by inducing permeability transition.

    Science.gov (United States)

    Bonke, Erik; Siebels, Ilka; Zwicker, Klaus; Dröse, Stefan

    2016-10-01

    Manganese-induced toxicity has been linked to mitochondrial dysfunction and an increased generation of reactive oxygen species (ROS). We could recently show in mechanistic studies that Mn 2+ ions induce hydrogen peroxide (H 2 O 2 ) production from the ubiquinone binding site of mitochondrial complex II (II Q ) and generally enhance H 2 O 2 formation by accelerating the rate of superoxide dismutation. The present study with intact mitochondria reveals that manganese additionally enhances H 2 O 2 emission by inducing mitochondrial permeability transition (mPT). In mitochondria fed by NADH-generating substrates, the combination of Mn 2+ and different respiratory chain inhibitors led to a dynamically increasing H 2 O 2 emission which was sensitive to the mPT inhibitor cyclosporine A (CsA) as well as Ru-360, an inhibitor of the mitochondrial calcium uniporter (MCU). Under these conditions, flavin-containing enzymes of the mitochondrial matrix, e.g. the mitochondrial 2-oxoglutaratedehydrogenase (OGDH), were major sources of ROS. With succinate as substrate, Mn 2+ stimulated ROS production mainly at complex II, whereby the applied succinate concentration had a marked effect on the tendency for mPT. Also Ca 2+ increased the rate of H 2 O 2 emission by mPT, while no direct effect on ROS-production of complex II was observed. The present study reveals a complex scenario through which manganese affects mitochondrial H 2 O 2 emission: stimulating its production from distinct sites (e.g. site II Q ), accelerating superoxide dismutation and enhancing the emission via mPT which also leads to the loss of soluble components of the mitochondrial antioxidant systems and favors the ROS production from flavin-containing oxidoreductases of the Krebs cycle. Copyright © 2016 Elsevier Inc. All rights reserved.

  13. HWVP submerged bed scrubber waste treatment by ion exchange at high pH

    Energy Technology Data Exchange (ETDEWEB)

    Bray, L.A.; Carson, K.J.; Elovich, R.J.; Eakin, D.E.

    1996-03-01

    The Hanford Waste Vitrification Plant (HWVP) is expected to produce aqueous waste streams that will require further processing for cesium, strontium, and transuranic (TRU) removal prior to incorporation into grout. Fluor Daniel, Inc. has recommended that zeolite be added to these waste streams for adsorption of cesium (Cs) and strontium (Sr) following pH adjustment by sodium hydroxide (NAOH) addition. Filtration will then used to remove the TRU elements associated with the process solids and the zeolite containing the Cs and Sr.

  14. HWVP submerged bed scrubber waste treatment by ion exchange at high pH

    International Nuclear Information System (INIS)

    Bray, L.A.; Carson, K.J.; Elovich, R.J.; Eakin, D.E.

    1996-03-01

    The Hanford Waste Vitrification Plant (HWVP) is expected to produce aqueous waste streams that will require further processing for cesium, strontium, and transuranic (TRU) removal prior to incorporation into grout. Fluor Daniel, Inc. has recommended that zeolite be added to these waste streams for adsorption of cesium (Cs) and strontium (Sr) following pH adjustment by sodium hydroxide (NAOH) addition. Filtration will then used to remove the TRU elements associated with the process solids and the zeolite containing the Cs and Sr

  15. Coherent electron emission from H2 and Young type interference in swift ion and electron collisions

    Energy Technology Data Exchange (ETDEWEB)

    Misra, D.; Chatterjee, S.; Tribedi, Lokesh C. [Tata Institute of Fundamental Research, Colaba, Mumbai (India)

    2009-07-01

    The coherent electron emission from the inversion-symmetric homonuclear diatomic molecule H{sub 2}, carry the signature of the Young type electron interference. In a new approach we have shown that instead of taking H{sub 2}-to-2H DDCS ratios one can use the forward backward asymmetry in electron emission to obtain the oscillation due to interference. Bare fast C and F available from Pelletron accelerator at TIFR and 8 keV electron beam was used for these experiments. The frequency in 160 {sup circle} was found to be a factor of two higher w.r.t. 20 {sup circle}. The difference in the oscillation frequency for the forward and backward angles causes the oscillation in the asymmetry parameter. A model calculation based on Cohen-Fano model joined together with the frequency difference in forward-backward angles, fits the spectrum well. Since this study does not need any atomic target, can be applied for other diatomic molecular targets: a step forward towards the study of Young type interference in ionizations of molecule. Besides first order interference our data provides a strong support for the evidence of a double frequency component in interference oscillations.

  16. A Novel Coordination Polymer Constructed by Hetero-Metal Ions and 2,3-Pyridine Dicarboxylic Acid: Synthesis and Structure of [NiNa2(PDC)2(μ-H2O)(H2O)2] n

    Science.gov (United States)

    Dou, Ming-Yu; Lu, Jing

    2017-12-01

    A novel coordination polymer containing hetero-metal ions, [NiNa2(PDC)2(μ-H2O)(H2O)2] n , where PDC is 2,3-pyridine dicarboxylate ion, has been synthesized. In the structure, the PDC ligand chelates and bridges two Ni(II) and two Na(I) centers. Two kinds of metal centers are connected by μ4-PDC and μ2-H2O to form 2D coordination layers. Hydrogen bonds between coordination water molecules and carboxylate oxygen atoms further link these 2D coordination layers to form 3D supramolecular network.

  17. Liberation of H2 from (o-C6H4Me)3P—H(+) + (-)H—B(p-C6F4H)3 ion-pair: A transition-state in the minimum energy path versus the transient species in Born-Oppenheimer molecular dynamics

    Science.gov (United States)

    Pu, Maoping; Heshmat, Mojgan; Privalov, Timofei

    2017-07-01

    Using Born-Oppenheimer molecular dynamics (BOMD) with density functional theory, transition-state (TS) calculations, and the quantitative energy decomposition analysis (EDA), we examined the mechanism of H2-liberation from LB—H(+) + (-)H—LA ion-pair, 1, in which the Lewis base (LB) is (o-C6H4Me)3P and the Lewis acid (LA) is B(p-C6F4H)3. BOMD simulations indicate that the path of H2 liberation from the ion-pair 1 goes via the short-lived transient species, LB⋯H2⋯LA, which are structurally reminiscent of the TS-structure in the minimum-energy-path describing the reversible reaction between H2 and (o-C6H4Me)3P/B(p-C6F4H)3 frustrated Lewis pair (FLP). With electronic structure calculations performed on graphics processing units, our BOMD data-set covers more than 1 ns of evolution of the ion-pair 1 at temperature T ≈ 400 K. BOMD simulations produced H2-recombination events with various durations of H2 remaining fully recombined as a molecule within a LB/LA attractive "pocket"—from very short vibrational-time scale to time scales in the range of a few hundred femtoseconds. With the help of perturbational approach to trajectory-propagation over a saddle-area, we directly examined dynamics of H2-liberation. Using EDA, we elucidated interactions between the cationic and anionic fragments in the ion-pair 1 and between the molecular fragments in the TS-structure. We have also considered a model that qualitatively takes into account the potential energy characteristics of H—H recombination and H2-release plus inertia of molecular motion of the (o-C6H4Me)3P/B(p-C6F4H)3 FLP.

  18. Effect of elevated potassium ion concentrations on electrically evoked release of [3H]acetylcholine in slices of rat hippocampus

    International Nuclear Information System (INIS)

    Szerb, J.C.; Hadhazy, P.; Dudar, J.D.

    1978-01-01

    To establish the effect of raising the concentration of extracellular potassium ions on axonal conduction and transmitter release in a mammalian central pathway, the septohippocampal cholinergic tract, the rate of [ 3 H] acetylcholine release evoked by electrical stimulation was measured in rat hippocampal slices superfused with Krebs' solution containing 3-15 mM K + The evoked release of [ 3 H] acetylcholine was abolished by the presence of tetrodotoxin or by the omission of Ca 2+ in the superfusion medium, indicating that it originated from terminals depolarized by conducted action potentials. Potassium concentrations between 3 and 8 mM had no effect but 10-15 mM K + reduced the rate of evoked release and decreased the size of the releasable pool of [ 3 H] acetylcholine. Decreasing the sodium content of the Krebs' solution to 97 mM or less had effects similar to those of elevated [K + ]. Elevated K + (10-15 mM) reversibly reduced the size of compound action potentials in the fimbria and the alveus. The results suggest that extracellular potassium concentrations occurring under physiological conditions do not affect axonal conduction and transmitter release but that both are reduced in pathological states when extracellular [K + ] above 8 mM occur. (author)

  19. Dynamics of low to high (``L'' to ``H'') confinement bifurcation: Poloidal flow and ion pressure gradient evolution

    Science.gov (United States)

    Carreras, B. A.; Newman, D.; Diamond, P. H.; Liang, Y.-M.

    1994-12-01

    A self-consistent model of the low to high (``L'' to ``H'') transition is derived from coupled nonlinear envelope equations for the fluctuation level and radial electric field shear, Er', as determined by ion pressure gradient, ∇Pi, and poloidal flow. These equations extend the phase transition model of the L to H bifurcation by including ∇Pi effects. In this model, the transition occurs when the turbulence drive is large enough to overcome the damping of the total E×B flow. Near the critical power for transition, poloidal flow shear dominates Er', but at high power, ∇Pi gives the main contribution. The inclusion of ∇Pi also introduces a quenched fluctuation state that is accessible at high power and may be the experimentally observed H-mode state for P≫Pcrit. In this state, the radial electric field is determined only by ∇Pi because no fluctuation energy is available to produce a turbulent Reynolds stress.

  20. Stopping force and straggling of 0.6-4.7 MeV H, He and Li ions in the polyhydroxybutyrate foil

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, J.Y. [Institute of Physics, Academia Sinica, Taipei 11529, Taiwan (China); Yu, Y.C., E-mail: phycyu@phys.sinica.edu.t [Institute of Physics, Academia Sinica, Taipei 11529, Taiwan (China); Chen, K.M. [Institute of Physics, Academia Sinica, Taipei 11529, Taiwan (China)

    2010-06-15

    Stopping force and straggling of 0.6-3.5 MeV {sup 1}H ions, 2.0-4.7 MeV {sup 4}He ions and 1.4-4.4 MeV {sup 7}Li ions in the polyhydroxybutyrate (PHB) foil were measured by means of a transmission technique. The measured stopping forces are in well agreement with the SRIM 2008 calculation and the ICRU Report tables, except for the lower energy region. The obtained energy loss straggling deviates from the Bohr's value by as much as 23.6% for the energies under study. The validity of the Bragg's rule has also been demonstrated in the stopping force and straggling for {sup 1}H, {sup 4}He and {sup 7}Li ions in the PHB foil.

  1. Stopping force and straggling of 0.6-4.7 MeV H, He and Li ions in the polyhydroxybutyrate foil

    Science.gov (United States)

    Hsu, J. Y.; Yu, Y. C.; Chen, K. M.

    2010-06-01

    Stopping force and straggling of 0.6-3.5 MeV 1H ions, 2.0-4.7 MeV 4He ions and 1.4-4.4 MeV 7Li ions in the polyhydroxybutyrate (PHB) foil were measured by means of a transmission technique. The measured stopping forces are in well agreement with the SRIM 2008 calculation and the ICRU Report tables, except for the lower energy region. The obtained energy loss straggling deviates from the Bohr's value by as much as 23.6% for the energies under study. The validity of the Bragg's rule has also been demonstrated in the stopping force and straggling for 1H, 4He and 7Li ions in the PHB foil.

  2. Investigation of the critical edge ion heat flux for L-H transitions in Alcator C-Mod and its dependence on B T

    Science.gov (United States)

    Schmidtmayr, M.; Hughes, J. W.; Ryter, F.; Wolfrum, E.; Cao, N.; Creely, A. J.; Howard, N.; Hubbard, A. E.; Lin, Y.; Reinke, M. L.; Rice, J. E.; Tolman, E. A.; Wukitch, S.; Ma, Y.; ASDEX Upgrade Team; Alcator C-Mod Team

    2018-05-01

    This paper presents investigations on the role of the edge ion heat flux for transitions from L-mode to H-mode in Alcator C-Mod. Previous results from the ASDEX Upgrade tokamak indicated that a critical value of edge ion heat flux per particle is needed for the transition. Analysis of C-Mod data confirms this result. The edge ion heat flux is indeed found to increase linearly with density at given magnetic field and plasma current. Furthermore, the Alcator C-Mod data indicate that the edge ion heat flux at the L-H transition also increases with magnetic field. Combining the data from Alcator C-Mod and ASDEX Upgrade yields a general expression for the edge ion heat flux at the L-H transition. These results are discussed from the point of view of the possible physics mechanism of the L-H transition. They are also compared to the L-H power threshold scaling and an extrapolation for ITER is given.

  3. Analysis of H- ion trajectories in a space-charge lens

    International Nuclear Information System (INIS)

    Hess, G.R.; Humphries, S. Jr.

    1987-01-01

    The success of an electron, space-charge-corrected, solenoidal magnetic lens experiment encouraged the analysis of H - trajectories in a large model-corrected solenoid. With a confined distribution of low energy electrons, the selenoid magnetic flux surfaces define electric equipotential surfaces. The field contribution from trapped electrons cancel net axial electric fields. Negatively charged beam particles then experience a defocusing force which can alleviate spherical aberration. Regions of the magnetic field can be linked by individually biased potential rings to program the correcting electric field. Given a magnetic field distribution, the electric potential distribution required to numerically correct beam particle orbits can be used to determine these ring voltages. (orig.)

  4. Initial operation of the CW 8X H- ion source discharge

    International Nuclear Information System (INIS)

    Smith, H.V. Jr.; Allison, P.; Geisik, C.; Schmitt, D.R.; Schneider, J.D.; Stelzer, J.E.

    1993-01-01

    A pulsed 8Χ source was built and the H - beam current, emittance, and power efficiency were measured. These results were promising, so a cooled, dc version designed for operation at arc power levels up to 30 kW was built. Testing of the CW 8Χ source discharge is underway. The design dc power loading on the cathode surface is 900 W/cm 2 , considerably higher than achieved in any pervious Penning surface-plasma source (SPS). Thus, the electrode surfaces are cooled with pressurized, hot water. We describe the source and present the initial operating experience and arc test results

  5. Evaluation of Resin Regeneration Using HCl and H2SO4 for the Ion Exchanger of Copper

    International Nuclear Information System (INIS)

    Prayitno; Djoko Sardjono

    2002-01-01

    The experimental investigation on the regeneration of resin using HCl and H 2 SO 4 with its varian concentration of 1; 2.5; 2; 2.5 and 3 N and the stirring time was 5; 10; 15; 20; and 25 minutes. For evaluating their effectiveness on the separation of ion copper in the waste with concentration 500 ppm. Experimentally this investigation is the first step of resin results of regeneration process usage as an alternative resin for the treatment of liquid waste containing especially copper. The experimental resulted by mixing the feed copper waste with resin after regeneration. Therefore it could be concluded that the most effective regeneration was obtained with HCl as the regeneration of concentration 2 N and the stirring time 15 minutes with the percentage of separation used of 85.1 %. (author)

  6. Observation of high-lying resonances in the H sup minus ion

    Energy Technology Data Exchange (ETDEWEB)

    Harris, P.G. (Los Alamos National Lab., NM (USA) New Mexico Univ., Albuquerque, NM (USA). Dept. of Physics and Astronomy)

    1990-05-01

    This dissertation reports the observation of several series of resonances, for which both electrons are in excited states, in the photodetachment cross section of H{sup {minus}}. These {sup 1}P doubly-excited states interfere with the continuum in which they are embedded, and appear as dips in the production cross section of excited neutral hydrogen. The experiment was performed by intersecting an 800 MeV H{sup {minus}} beam with a (266 nm) laser beam at varying angles; the relativistic Doppler shift then tuned'' the photon energy in the barycentric frame. The process was observed by using a magnet strong enough the strip the electrons from the excited hydrogen atoms in selected states n and detecting the resulting protons, which allowed the isolation of the individual n channels. Three resonances are clearly visible in each channel. The data support recent theoretical calculations for the positions of doubly-excited {sup 1}P resonances, and verify a new Rydberg-like formula for the modified Coulomb potential.

  7. Effect of exposed surface area, volume and environmental pH on the calcium ion release of three commercially available tricalcium silicate based dental cements

    OpenAIRE

    Rajasekharan, Sivaprakash; Vercruysse, Chris; Martens, Luc; Verbeeck, Ronald

    2018-01-01

    Tricalcium silicate cements (TSC) are used in dental traumatology and endodontics for their bioactivity which is mostly attributed to formation of calcium hydroxide during TSC hydration and its subsequent release of calcium and hydroxide ions. The aim of this study was to determine the effect of volume (Vol), exposed surface area (ESA) and pH of surrounding medium on calcium ion release. Three commercially available hydraulic alkaline dental cements were mixed and condensed into cylindrical t...

  8. Transition metal ions and selenite modulate the methylation of arsenite by the recombinant human arsenic (+3 oxidation state) methyltransferase (hAS3MT).

    Science.gov (United States)

    Song, Xiaoli; Geng, Zhirong; Li, Chengying; Hu, Xin; Wang, Zhilin

    2010-05-01

    This report demonstrates that transition metal ions and selenite affect the arsenite methylation by the recombinant human arsenic (+3 oxidation state) methyltransferase (hAS3MT) in vitro. Co(2+), Mn(2+), and Zn(2+) inhibited the arsenite methylation by hAS3MT in a concentration-dependent manner and the kinetics indicated Co(2+) and Mn(2+) to be mixed (competitive and non-competitive) inhibitors while Zn(2+) to be a competitive inhibitor. However, only a high concentration of Fe(2+) could restrain the methylation. UV-visible, CD and fluorescence spectroscopy were used to study the interactions between the metal ions above and hAS3MT. Further studies showed that neither superoxide anion nor hydrogen peroxide was involved in the transition metal ion or selenite inhibition of hAS3MT activity. The inhibition of arsenite methylating activity of hAS3MT by selenite was reversed by 2mM DTT (dithiothreitol) but neither by cysteine nor by beta-mercaptoethanol. Whereas, besides DTT, cysteine can also prevent the inhibition of hAS3MT activity by Co(2+), Mn(2+), and Zn(2+). Free Cys residues were involved in the interactions of transition metal ions or selenite with hAS3MT. It is proposed that the inhibitory effect of the ions (Co(2+), Mn(2+), and Zn(2+)) or selenite on hAS3MT activity might be via the interactions of them with free Cys residues in hAS3MT to form inactive protein adducts.

  9. The formation of [M-H]+ ions in N-alkyl-substituted thieno[3,4-c]-pyrrole-4,6-dione derivatives during atmospheric pressure photoionization mass spectrometry

    KAUST Repository

    Sioud, Salim

    2014-10-09

    RESULTS [M-H]+ ions were observed under APPI conditions. The type of dopant and the length of the alkyl chain affected the formation of these ions. MS/MS fragmentation of [M-H]+ and [M + H]+ ions exhibited completely different patterns. Theoretical calculations revealed that the loss of hydrogen molecules from the [M + H]+ ions is the most favourable condition under which to form [M-H]+ ions.CONCLUSIONS [M-H]+ ions were detected in all the TPD derivatives studied here under the special experimental conditions during APPI, using a halogenated benzene dopant, and TPD containing substituted N-alkyl side chains with a minimum of four carbon atoms. Density functional theory calculations showed that for [M-H]+ ions to be formed under these conditions, the loss of hydrogen molecules from the [M + H]+ ions is proposed to be necessary.RATIONALE The formation of ions during atmospheric pressure photoionization (APPI) mass spectrometry in the positive mode usually provides radical cations and/or protonated species. Intriguingly, during the analysis of some N-alkyl-substituted thieno[3,4-c]pyrrole-4,6-dione (TPD) derivatives synthesized in our laboratory, unusual [M-H]+ ion peaks were observed. In this work we investigate the formation of [M-H]+ ions observed under APPI conditions.METHODS Multiple experimental parameters, including the type of ionization source, the composition of the solvent, the type of dopant, the infusion flow rate, and the length of the alkyl side chain were investigated to determine their effects on the formation of [M-H]+ ions. In addition, a comparison study of the gas-phase tandem mass spectrometric (MS/MS) fragmentation of [M + H]+ vs [M-H]+ ions and computational approaches were used.

  10. Inhibition by divalent metal ions of human histidine triad nucleotide binding protein1 (hHint1), a regulator of opioid analgesia and neuropathic pain.

    Science.gov (United States)

    Shah, Rachit; Chou, Tsui-Fen; Maize, Kimberly M; Strom, Alexander; Finzel, Barry C; Wagner, Carston R

    2017-09-23

    Human histidine triad nucleotide binding protein 1 (hHint1) is a purine nucleoside phosphoramidase and adenylate hydrolase that has emerged as a potential therapeutic target for the management of pain. However, the molecular mechanism of Hint1 in the signaling pathway has remained less clear. The role of metal ions in regulating postsynaptic transmission is well known, and the active site of hHint1 contains multiple histidines. Here we have investigated the effect of divalent metal ions (Cd 2+ , Cu 2+ , Mg 2+ , Mn 2+ , Ni 2+ , and Zn 2+ ) on the structural integrity and catalytic activity of hHint1. With the exception of Mg 2+ , all the divalent ions inhibited hHint1, the rank of order was found to be Cu 2+ >Zn 2+ >Cd 2+ ≥Ni 2+ >Mn 2+ based on their IC 50 and k in /K I values. A crystal structure of hHint1 with bound Cu 2+ is described to explain the competitive reversible inactivation of hHint1 by divalent cations. All the metal ions exhibited time- and concentration- dependent inhibition, with the rate of inactivation highly dependent on alterations of the C-terminus. With the exception of Cu 2+ ; restoration of inhibition was observed for all the metal ions after treatment with EDTA. Our studies reveal a loss in secondary structure and aggregation of hHint1 upon incubation with 10-fold excess of copper. Thus, hHint1 appears to be structurally sensitive to irreversible inactivation by copper, which may be of neurotoxicological and pharmacological significance. Copyright © 2017 Elsevier Inc. All rights reserved.

  11. Accumulation and Recovery of Disorder on Silicon and Carbon Sublattices in Ion-Irradiated 6H-SiC

    International Nuclear Information System (INIS)

    Jiang, Weilin; Weber, William J.; Thevuthasan, Suntharampillai; Shutthanandan, V.

    2001-01-01

    Irradiation experiments have been performed at 100, 170 and 300 K for 6H-SiC single crystals using Au and He+ ions over a range of fluences. The evolution of disorder on the both Si and C sublattices has been simultaneously investigated using 0.94 MeV D Rutherford backscattering spectrometry in combination with 12C(d,p) nuclear reaction analysis in a axial channeling geometry. The results show that the dependence of disorder on dose is consistent with a combined direct-impact / defect-stimulated model. At low doses, a slightly higher rate of C disordering is observed, which is consistent with molecular dynamics simulations that suggest a smaller threshold displacement energy on the C sublattice. At higher doses, the rate of C disordering decreases more rapidly than the rate of Si disordering, which suggests a higher rate of dynamical recovery on the C sublattice under the irradiation conditions. Three distinct recovery stages are observed on both the Si and C sublattices in the Au-irradiated 6H-SiC. However, complete recovery of irradiation-induced disorder does not occur during isochronal annealing at temperatures up to 970 K

  12. Aluminum surface corrosion and the mechanism of inhibitors using pH and metal ion selective imaging fiber bundles.

    Science.gov (United States)

    Szunerits, Sabine; Walt, David R

    2002-02-15

    The localized corrosion behavior of a galvanic aluminum copper couple was investigated by in situ fluorescence imaging with a fiber-optic imaging sensor. Three different, but complementary methods were used for visualizing remote corrosion sites, mapping the topography of the metal surface, and measuring local chemical concentrations of H+, OH-, and Al3+. The first method is based on a pH-sensitive imaging fiber, where the fluorescent dye SNAFL was covalently attached to the fiber's distal end. Fluorescence images were acquired as a function of time at different areas of the galvanic couple. In a second method, the fluorescent dye morin was immobilized on the fiber-optic imaging sensor, which allowed the in situ localization of corrosion processes on pure aluminum to be visualized over time by monitoring the release of Al3+. The development of fluorescence on the aluminum surface defined the areas associated with the anodic dissolution of aluminum. We also investigated the inhibition of corrosion of pure aluminum by CeCl3 and 8-hydroxyquinoline. The decrease in current, the decrease in the number of active sites on the aluminum surface, and the faster surface passivation are all consistent indications that cerium chloride and 8-hydroxyquinoline inhibit corrosion effectively. From the number and extent of corrosion sites and the release of aluminum ions monitored with the fiber, it was shown that 8-hydroxyquinoline is a more effective inhibitor than cerium chloride.

  13. Microscopic evaluation of nuclear foci (gamma H2AX) in cells irradiated with protons and lithium ions

    International Nuclear Information System (INIS)

    Bracalente, C.; Molinari, Beatriz L.; Duran, Hebe; Ibanez, I.; Palmieri, M.; Kreiner, Andres J.; Burlon, Alejandro; Valda, Alejandro; Davidson, J.; Davidson, M.; Vazquez, Monica; Ozafran, Mabel J.

    2007-01-01

    Full text: The special properties of both physical and biological radiation particles with high-LET (Linear Transfer of Energy) have led to its increased use in cancer therapy. In this work, the effect of high and low LET radiation on cell lines with different radiosensitivity (Irs-20 and CHO-10B2) quantifying the number and size of nuclear foci obtained from histone H2AX (γH2AX) phosphorylation which plays an important role in DNA damage reparation is compared. Foci detection was performed by immunocytochemical methods and fluorescence microscopy. The cells cultures were irradiated with plateau-phase protons (14 MeV, LET: 3 keV/μ), on Bragg peak (3 MeV. LET: 14 KeV/μ) and with Lithium ions (7 MeV, LET: 250 KeV//μ) on the Tandar accelerator. A clonogenic analysis of the two cell lines was made. Irradiation with protons (low LET) showed a significant difference (p [es

  14. Finite Forward Acceptance Angles for Single Electron Capture by ^3He^2+ Ions in He and H_2

    Science.gov (United States)

    Mawhorter, Rj; Greenwood, J.; Smith; Chutjian, A.

    2004-05-01

    Perhaps surprisingly, electron capture scattering angles of a few degrees or more are observed for slow ions impacting light targets. Gas cells must be designed with this in mind. Indeed the difference between small acceptance angle results(W.L. Nutt, et al., J. Phys. B 8), 1457 (1978) and the larger acceptance-angle studies of both Kusakabe, et al.(T. Kusakabe, et al., J. Phys. Soc. Japan 59), 1218 (1990) and our group at JPL (presented here; energy range 0.33-4.67 keV/amu) for ^3He^2+ in H2 can be ascribed to this effect. Olson and Kimura(R. E. Olson and M. Kimura, J. Phys. B 15), 4231 (1982) have modeled the problem theoretically. We use existing differential cross section data(D. Bordenave-Montesquieu and R. Dagnac, J. Phys. B 27), 543 1994) for both H_2/ D2 and ^4He targets to calculate realistic acceptance angles. The resulting small total cross section corrections provide reliable absolute results for these benchmark systems. This work was carried out at JPL/Caltech, and was supported through agreement with NASA.

  15. The fragment ion C13H9O2 m/z 197 in the mass spectra of 2-(2'-R-phenyl)benzoic acids

    International Nuclear Information System (INIS)

    Gills, R.G.; Porter, Q.N.

    1990-01-01

    In the electron impact mass spectrum of 2-( ' -R-phenyl)benzoic acids where R = H, NO 2 , OCH 3 , COOH, or Br, and abundant fragment ion m/z 197 is formed by an ipso substitution in which R is expelled as a radical. The structure of the ion m/z 197 has been shown by collision-activated dissociation to be identical with that of the protonated molecule formed by methane chemical ionization of 6H-dibenzo[b,d]pyran-6-one. 11 refs., 1 fig., ills

  16. Complementary metal ion specificity of the metal-citrate transporters CitM and CitH of Bacillus subtilis

    NARCIS (Netherlands)

    Krom, BP; Warner, JB; Konings, WN; Lolkema, JS; Warner, Jessica B.

    2000-01-01

    Citrate uptake in Bacillus subtilis is stimulated by a wide range of divalent metal ions. The metal ions were separated into two groups based on the expression pattern of the uptake system. The two groups correlated with the metal ion specificity of two homologous B, subtilis secondary citrate

  17. THE INFLUENCE OF pH TOWARDS MULTIPLE METAL ION ADSORPTION OF Cu(II, Zn(II, Mn(II, AND Fe(II ON HUMIC ACID

    Directory of Open Access Journals (Sweden)

    Buhani Buhani

    2010-06-01

    Full Text Available Multiple metal ions adsorption of Cu(II, Zn(II, Mn(II and Fe(II on humic acid with a batch method has been carried out at pH interaction of 3, 5, and 6. Concentration of metal ions in solution before and after interaction was analyzed with Atomic Absorption Spectrophotometer (AAS. Result showed that adsorption multiple metal ions of Cu(II, Zn(II, Mn(II, and Fe(II on humic acid is optimum at pH 5. Adsorption energies of the multiple metal ions Cu(II, Zn(II, Mn(II, and Fe(II on humic acid at pH 3, 5, and 6 are around 35.0 - 37.6 kJ/mole. In general, capacity of competition adsorption of the multiple metal ions has an order as follows; Cu(II < Fe(II < Zn(II < Mn(II.   Keywords: Humic acid, adsorption, multiple metal

  18. Gas-phase reactions of the bare Th2+ and U2+ ions with small alkanes, CH4, C2H6, and C3H8: experimental and theoretical study of elementary organoactinide chemistry.

    Science.gov (United States)

    Di Santo, Emanuela; Santos, Marta; Michelini, Maria C; Marçalo, Joaquim; Russo, Nino; Gibson, John K

    2011-02-16

    The gas-phase reactions of two dipositive actinide ions, Th(2+) and U(2+), with CH(4), C(2)H(6), and C(3)H(8) were studied by both experiment and theory. Fourier transform ion cyclotron resonance mass spectrometry was employed to study the bimolecular ion-molecule reactions; the potential energy profiles (PEPs) for the reactions, both observed and nonobserved, were computed by density functional theory (DFT). The experiments revealed that Th(2+) reacts with all three alkanes, including CH(4) to produce ThCH(2)(2+), whereas U(2+) reacts with C(2)H(6) and C(3)H(8), with different product distributions than for Th(2+). The comparative reactivities of Th(2+) and U(2+) toward CH(4) are well explained by the computed PEPs. The PEPs for the reactions with C(2)H(6) effectively rationalize the observed reaction products, ThC(2)H(2)(2+) and UC(2)H(4)(2+). For C(3)H(8) several reaction products were experimentally observed; these and additional potential reaction pathways were computed. The DFT results for the reactions with C(3)H(8) are consistent with the observed reactions and the different products observed for Th(2+) and U(2+); however, several exothermic products which emerge from energetically favorable PEPs were not experimentally observed. The comparison between experiment and theory reveals that DFT can effectively exclude unfavorable reaction pathways, due to energetic barriers and/or endothermic products, and can predict energetic differences in similar reaction pathways for different ions. However, and not surprisingly, a simple evaluation of the PEP features is insufficient to reliably exclude energetically favorable pathways. The computed PEPs, which all proceed by insertion, were used to evaluate the relationship between the energetics of the bare Th(2+) and U(2+) ions and the energies for C-H and C-C activation. It was found that the computed energetics for insertion are entirely consistent with the empirical model which relates insertion efficiency to the

  19. Autoionization dynamics of excited collision systems: Angular dependence of the electron and ion energy spectra for He*(23S)+H

    International Nuclear Information System (INIS)

    Merz, A.; Ruf, M.; Hotop, H.

    1992-01-01

    We present the first angle-dependent energy spectra for the basic autoionization process He * (2 3 S)+H(1 2 S) leading to Penning ionization (→He+H + +e - ; PI) and associative ionization [→HeH + (v + ,J + )+e - ; AI]. Our results include electron energy spectra for both reaction channels and the H + -ion energy spectra for PI. The variation of the electron spectra with angle demonstrates the presence of substantial contributions from non-s-type electron partial waves, with the angle-dependent electron signals due to AI yielding clear information on the internal electron angular distribution of the autoionizing quasimolecule

  20. Investigations towards multi-step laser spectroscopy of stored H{sub 3}{sup +} molecular ions; Untersuchungen zur Mehrstufen-Laserspektroskopie an gespeicherten H{sub 3}{sup +}-Molekuelionen

    Energy Technology Data Exchange (ETDEWEB)

    Bing, Dennis

    2010-07-21

    The triatomic H{sub 3}{sup +} molecular ion plays an important role in molecular quantum dynamics through its equilateral triangular structure. Many studies of molecular reactions involving H{sub 3}{sup +} have been done thus far, among them dissociative recombination in storage ring experiments with a cold electron-beam. For these strongly energy dependent reactions, the population in individual rovibrational levels is of large importance. To determine such populations for H{sub 3}{sup +} ions inside a storage ring, an extremely sensitive state-selective method must be used, such as the Resonant- Enhanced Multi-Photon Dissociation (REMPD). In REMPD, molecules are highly excited from a low lying initial level in a first resonant step and photodissociated from these high lying states in a second step. To fully employ this method, detailed investigations are necessary. Here, an experiment is presented which determines the energy range of the highly excited vibrational states of H{sub 3}{sup +} suitable for photodissociation. Additional photodissociation experiments, using hot H{sub 3}{sup +} ions in the storage ring TSR at the Max-Planck Institute for Nuclear Physics, yield an effective lifetime of these dissociated H{sub 3}{sup +} states. Finally selective vibrational excitation of cold H{sub 3}{sup +} (the rst step of REMPD) is discussed with the aim of reaching the highly excited vibrational states suitable for photodissociation. (orig.)

  1. Effect of Mobile Phone Usage on Nickel Ions Release and pH of Saliva in Patients Undergoing Fixed Orthodontic Treatment.

    Science.gov (United States)

    Nanjannawar, Lalita Girish; Girme, Tejashree Suresh; Agrawal, Jiwanasha Manish; Agrawal, Manish Suresh; Fulari, Sangamesh Gurunath; Shetti, Shraddha Subhash; Kagi, Vishwal Ajith

    2017-09-01

    Hand held mobile phones are presently the most popular means of communication worldwide and have transformed our lives in many aspects. The widespread use of such devices have resulted in growing concerns regarding harmful effects of radiations emitted by them. This study was designed to evaluate the effects of mobile phone usage on nickel ion release as well as pH of saliva in patients with fixed orthodontic appliances. To assess the level of nickel ions in saliva and pH of saliva in mobile phone users undergoing fixed orthodontic treatment using inductively coupled plasma atomic emission spectrometry. A total of 42 healthy patients with fixed orthodontic appliance in mouth for a duration of six to nine months were selected for the study. They were divided into experimental group (n=21) consisting of mobile phone users and control group (n=21) of non mobile phone users. Saliva samples were collected from both the groups and nickel ion levels were measured using inductively coupled plasma-mass spectroscopy. The pH values were also assessed for both groups using pH meter. Unpaired t-test was used for the data analysis. Statistical analysis revealed that though the pH levels were reduced and the nickel ion levels were higher in the experimental group compared to the control group, the results were non significant. Mobile phone usage may affect the pH of saliva and result in increased release of nickel ions in saliva of patients with fixed orthodontic appliances in the oral cavity.

  2. Selective capillary diffusion of equimolar H2/D2 gas mixtures through etched ion track membranes prepared from polyethylene terephthalate and polyimide

    International Nuclear Information System (INIS)

    Schmidt, K.; Angert, N.; Trautmann, C.

    1996-01-01

    The selective capillary diffusion of equimolar H 2 /D 2 gas mixtures through ion track membranes prepared from polyethylene terephthalate and polyimide was investigated at a temperature of 293 K, a primary pressure of 0.15 MPa and a secondary pressure of 10 -4 MPa. Different values of the separation factor Z(H 2 /D 2 ) between experiment and computer simulation exists in the case of polyethylene terephthalate ion track membranes because of multiple pores. Membranes for which multiple pores were reduced by varying the irradiation angle showed an increased separation factor. The separation factor is a function of the pore diameter. This is shown for polyimide ion track membranes with a pore size in the range of 0.17 and 0.5 μm. After grafting with styrene the separation factor increased, indicating grafting within the pores. (orig.)

  3. Fabrication of SGOI material by oxidation of an epitaxial SiGe layer on an SOI wafer with H ions implantation

    International Nuclear Information System (INIS)

    Cheng Xinli; Chen Zhijun; Wang Yongjin; Jin Bo; Zhang Feng; Zou Shichang

    2005-01-01

    SGOI materials were fabricated by thermal dry oxidation of epitaxial H-ion implanted SiGe layers on SOI wafers. The hydrogen implantation was found to delay the oxidation rate of SiGe layer and to decrease the loss of Ge atoms during oxidation. Further, the H implantation did not degrade the crystallinity of SiGe layer during fabrication of the SGOI

  4. A simple triazole-based “turn on” fluorescent sensor for Al3+ ion in MeCN–H2O and F− ion in MeCN

    International Nuclear Information System (INIS)

    Erdemir, Serkan; Malkondu, Sait

    2015-01-01

    A novel fluorescent sensor N-((2-hydroxynaphthalen-1-yl)methylene)-1H-1,2,4-triazole-3-carbohydrazide (NTA), based on triazole was synthesized in two facile steps, characterized systematically and used as a turn-on fluorescent sensor for both Al 3+ and F − . The fluorescence spectra changes showed that NTA is highly selective for Al 3+ over other metal ions in MeCN–H 2 O solution. The receptor NTA could also sense F − selectively in MeCN. The complexation properties of receptor NTA with Al 3+ and F − ions were observed by 1 H NMR titration experiments. - Highlights: • A novel fluorescent sensor based on triazole was synthesized in two steps and fully characterized. • The optical properties of NTA were observed by UV–visible and fluorescence spectroscopy. • NTA showed high selectivity and sensitivity to Al 3+ cation and F − anion

  5. Tribological properties of nc-TiC/a-C : H coatings prepared by magnetron sputtering at low and high ion bombardment of the growing film

    NARCIS (Netherlands)

    Souček, Pavel; Schmidtová, Tereza; Buršíková, Vilma; Vašina, Petr; Pei, Y.T.; Hosson, J.Th.M. De; Caha, Ondřej; Peřina, Vratislav; Mikšová, Romana; Malinský, Petr

    2014-01-01

    Two series of nc-TiC/a-C:H coatings were deposited by a hybrid PVD–PECVD process of titanium sputtering in argon/acetylene atmosphere at two configurations of magnetic field resulting in different impinging ion fluxes on the growing film. The composition of the coatings was varied by changing the

  6. Evaluating the role of metal ions in the bathochromic and hyperchromic responses of cyanidin derivatives in acidic and alkaline pH.

    Science.gov (United States)

    Sigurdson, G T; Robbins, R J; Collins, T M; Giusti, M M

    2016-10-01

    In many food products, colorants derived from natural sources are increasingly popular due to consumer demand. Anthocyanins are one class of versatile and abundant naturally occurring chromophores that produce different hues in nature, especially with metal ions and other copigments assisting. The effects of chelation of metal ions (Mg(2+), Al(3+), Cr(3+), Fe(3+), and Ga(3+)) in factorial excesses to anthocyanin concentration (0-500×) on the spectral characteristics (380-700nm) of cyanidin and acylated cyanidin derivatives were evaluated to better understand the color evolution of anthocyanin-metal chelates in pH 3-8. In all pH, anthocyanins exhibited bathochromic and hyperchromic shifts. Largest bathochromic shifts most often occurred in pH 6; while largest hyperchromic shifts occurred in pH 5. Divalent Mg(2+) showed no observable effect on anthocyanin color while trivalent metal ions caused bathochromic shifts and hue changes. Generally, bathochromic shifts on anthocyanins were greatest with more electron rich metal ions (Fe(3+)≈Ga(3+)>Al(3+)>Cr(3+)). Copyright © 2016 Elsevier Ltd. All rights reserved.

  7. Cross sections for one-electron capture by highly stripped ions of Be, B and C from H2 and Ar below 10 keV

    International Nuclear Information System (INIS)

    Takagi, S.; Ohtani, S.; Kadota, K.; Fujita, J.

    1982-03-01

    Cross sections for one-electron capture by highly stripped ions of Be, B and C from H 2 and Ar are measured at low energies below 10 keV. The cross sections are nearly independent of the collision energy investigated. The distinct oscillation with incident ionic charge g in the cross sections are observed. (author)

  8. Application of NIR - CRDS for state selective study of recombination of para and ortho H{sub 3}{sup +} ions with electrons in low temperature plasma

    Energy Technology Data Exchange (ETDEWEB)

    Varju, J; Roucka, S; KotrIk, T; Plasil, R; Glosik, J, E-mail: Juraj.Glosik@mff.cuni.c [Charles University, Faculty of Mathematics and Physics, Department of Surface and Plasma Science, V Holesovickach 2, Prague 8 (Czech Republic)

    2010-05-01

    We present a study of H{sub 3}{sup +} recombination performed at 77 K on the two lowest rotational levels of this ion, which belong to its two different nuclear spin states of the studied ion. A near infrared cavity ring-down spectrometer ({approx}1381 nm, CRDS arrangement) has been used to obtain the time evolution of concentration of both states. From the overall ion density decay during the afterglow we obtained the binary recombination rate coefficient {alpha}{sub bin} (77 K) = 1.2x10{sup -7} cm{sup 3}s{sup -1}. We have also observed ternary helium assisted recombination of both para and ortho H{sub 3}{sup +}. The process is very slow (at 77 K) and the obtained ternary recombination rate coefficient is in contradiction with the theoretical prediction. It is the first time that the binary and ternary H{sub 3}{sup +} recombination rate coefficient was measured at a known population of para and ortho H{sub 3}{sup +} ions in decaying plasma.

  9. Anomalous alignment dependence of the third-order harmonic of H2+ ions in intense laser fields

    Science.gov (United States)

    Jin, Ying-Jun; Tong, Xiao-Min; Toshima, Nobuyuki

    2012-11-01

    We studied the high-harmonic generation of H2+ ions in an intense laser field by solving the time-dependent Schrödinger equation in prolate spheroidal coordinates. By analyzing the power spectra of the harmonics with the electric field polarized along the molecular axis, we found that the yield of the third-order harmonic drops by several orders of magnitude at a specified aligned angle between the laser polarization direction and the molecular axis. The laser polarization angle of the minimum depends on the internuclear distance and it disappears both in the separated- and united-atom limits. This infers that the minimum is associated with the molecular symmetry. By decomposing individual contributions of the σ and π states, we identified that the minimum is attributed to the cancellation of the induced dipole moments of the σ and π states, like a dynamical Cooper minimum, but the position of the minimum can be tuned by the laser intensity for a given internuclear distance.

  10. Mecanismos cinéticos y distribuciones energéticas de iones (H3+, N2H+, CH3+...) en plasmas fríos de H2/N2/CH4

    Science.gov (United States)

    Tanarro, I.; Herrero, V. J.; Islyaikin, A.; Tabarés, F. L.; Tafalla, D.

    En este trabajo se presenta el estudio espectrométrico de los plasmas levemente ionizados generados en una descarga continua a baja presión de H2 con trazas de N2 y CH4, orientado principalmente a identificar la naturaleza y distribución energética de los iones que en ella se producen, y a asignar algunos de los mecanismos cinéticos elementales de formación y destrucción de tales especies. Alguno de los iones mayoritarios de estos plasmas, como el H3+, presenta gran interés desde el punto de vista de la Astrofísica por su prevista intervención en la química de las ionosferas planetarias y del medio interestelar, al actuar como sustancia intermedia en la formación de gran variedad de especies moleculares; si bien, dada su pequeña concentración, su observación real en el espacio se demoró hasta la pasada década de los años 90, cuando fue detectado por primera vez en la atmósfera de Júpiter y en otros objetos estelares. Del mismo modo que los trabajos espectroscópicos de laboratorio resultan indispensables para la posterior identificación de las especies observadas en el espacio, es de esperar que la asignación de los procesos cinéticos más importantes que tienen lugar en los plasmas generados en reactores de descarga, como los aquí presentados, permitan extrapolar los resultados así obtenidos al esclarecimiento de los mecanismos fisico-químicos participantes en otros medios observables únicamente a larga distancia.

  11. Setup and proof of principle of SAPIS (Stored Atoms Polarized Ion Source), a novel source of polarized H{sup -}/D{sup -} ions; Aufbau und Funktionsnachweis von SAPIS (Stored Atoms Polarized Ion Source), einer neuartigen Quelle polarisierter H{sup -}/D{sup -}-Ionen

    Energy Technology Data Exchange (ETDEWEB)

    Emmerich, R.

    2007-02-14

    The objective of this work was the setup and the proof-of-principle of a new type of negative polarized hydrogen or deuterium ion source, which is based on the charge-exchange reaction (vector)H{sup 0}+Cs{sup 0}{yields}(vector)H{sup -}+Cs{sup +}, as for instance the Colliding-Beams-Source (CBS) at the Cooler Synchrotron COSY in Juelich. In contrast to the CBS, the use of a storage cell for the charge-exchange region promises an increase in H{sup -} current by at least an order of magnitude without considerable polarization losses. For these purposes, a new laboratory was equipped and both a polarized hydrogen/deuterium atomic beam source and an intense neutral cesium-beam source have been build-on. A Lambshift polarimeter, which allows the measurement of the nuclear polarization of the atomic as well as ionic beams, was completed with the construction of a new spin-filter. After commissioning and optimizing each of these sources, a storage cell was developed and installed in the charge-exchange region with a magnetic field. Additionally, components for the extraction, detection and analysis of the negative ion beam were installed. Following the decisive proof of principle, investigation of the properties of the storage cell, especially as to H recombination and depolarisation, was begun. Furthermore, a number of software programs was developed for the control and monitoring of different components of the sources as well as a universal measuring software for the complete installation, including the measurement and calculation of the beam polarization. At the same time, the remote control system of the Cologne source of polarized ions LASCO at the FN tandem accelerator was completely modernized. (orig.)

  12. Using fluorescence measurement of zinc ions liberated from ZnS nanoparticle labels in bioassay for Escherichia coli O157:H7

    International Nuclear Information System (INIS)

    Cowles, Chad L.; Zhu Xiaoshan; Pai, Chi-Yun

    2011-01-01

    In this study, an alternative approach using ZnS nanoparticle biolabels as fluorescence signal transducers is reported for the immunoassay of E. coli O157:H7 in tap water samples. Instead of measuring the fluorescence of ZnS nanoparticles in the assay, the fluorescence signal is generated through the binding of zinc ions released from nanoparticle labels with zinc-ion sensitive fluorescence indicator Fluozin-3. In the assay, ZnS nanoparticles around 50 nm in diameter were synthesized, bioconjugated, and applied for the detection of E. coli O157:H7. The assay shows a detection range over two orders of magnitude and a detection limit around 1000 colony-forming units (cfu) of E. coli O157:H7.

  13. Effect of liquid gate bias rising time in pH sensors based on Si nanowire ion sensitive field effect transistors

    Science.gov (United States)

    Jang, Jungkyu; Choi, Sungju; Kim, Jungmok; Park, Tae Jung; Park, Byung-Gook; Kim, Dong Myong; Choi, Sung-Jin; Lee, Seung Min; Kim, Dae Hwan; Mo, Hyun-Sun

    2018-02-01

    In this study, we investigate the effect of rising time (TR) of liquid gate bias (VLG) on transient responses in pH sensors based on Si nanowire ion-sensitive field-effect transistors (ISFETs). As TR becomes shorter and pH values decrease, the ISFET current takes a longer time to saturate to the pH-dependent steady-state value. By correlating VLG with the internal gate-to-source voltage of the ISFET, we found that this effect occurs when the drift/diffusion of mobile ions in analytes in response to VLG is delayed. This gives us useful insight on the design of ISFET-based point-of-care circuits and systems, particularly with respect to determining an appropriate rising time for the liquid gate bias.

  14. A new H2+ source: Conceptual study and experimental test of an upgraded version of the VIS—Versatile ion source

    Science.gov (United States)

    Castro, G.; Torrisi, G.; Celona, L.; Mascali, D.; Neri, L.; Sorbello, G.; Leonardi, O.; Patti, G.; Castorina, G.; Gammino, S.

    2016-08-01

    The versatile ion source is an off-resonance microwave discharge ion source which produces a slightly overdense plasma at 2.45 GHz of pumping wave frequency extracting more than 60 mA proton beams and 50 mA He+ beams. DAEδALUS and IsoDAR experiments require high intensities for H2+ beams to be accelerated by high power cyclotrons for neutrinos generation. In order to fulfill the new requirements, a new plasma chamber and injection system has been designed and manufactured for increasing the H2+ beam intensity. In this paper the studies for the increasing of the H2+/p ratio and for the design of the new plasma chamber and injection system will be shown and discussed together with the experimental tests carried out at Istituto Nazionale di Fisica Nucleare-Laboratori Nazionali del Sud (INFN-LNS) and at Best Cyclotron Systems test-bench in Vancouver, Canada.

  15. Highly Durable Na2V6O16·1.63H2O Nanowire Cathode for Aqueous Zinc-Ion Battery.

    Science.gov (United States)

    Hu, Ping; Zhu, Ting; Wang, Xuanpeng; Wei, Xiujuan; Yan, Mengyu; Li, Jiantao; Luo, Wen; Yang, Wei; Zhang, Wencui; Zhou, Liang; Zhou, Zhiqiang; Mai, Liqiang

    2018-03-14

    Rechargeable aqueous zinc-ion batteries are highly desirable for grid-scale applications due to their low cost and high safety; however, the poor cycling stability hinders their widespread application. Herein, a highly durable zinc-ion battery system with a Na 2 V 6 O 16 ·1.63H 2 O nanowire cathode and an aqueous Zn(CF 3 SO 3 ) 2 electrolyte has been developed. The Na 2 V 6 O 16 ·1.63H 2 O nanowires deliver a high specific capacity of 352 mAh g -1 at 50 mA g -1 and exhibit a capacity retention of 90% over 6000 cycles at 5000 mA g -1 , which represents the best cycling performance compared with all previous reports. In contrast, the NaV 3 O 8 nanowires maintain only 17% of the initial capacity after 4000 cycles at 5000 mA g -1 . A single-nanowire-based zinc-ion battery is assembled, which reveals the intrinsic Zn 2+ storage mechanism at nanoscale. The remarkable electrochemical performance especially the long-term cycling stability makes Na 2 V 6 O 16 ·1.63H 2 O a promising cathode for a low-cost and safe aqueous zinc-ion battery.

  16. Mechanism of oxalate ion adsorption on chromium oxide-hydroxide from pH dependence and time evolution of ATR-IR spectra

    Science.gov (United States)

    Degenhardt, Jens; McQuillan, A. James

    1999-09-01

    A chromium (III) oxide-hydroxide colloid film has been used to model the passive surface of stainless steel in in situ ATR-IR studies of oxalate ion adsorption from aqueous oxalate solutions over a wide pH range. Studies of time and pH dependence of adsorption have been used to reveal a mechanism of adsorption proceeding through ionic, hydrogen bonded and coordinated oxalate species. A Langmuir adsorption constant of 4.5×10 4 M -1 was determined for the surface coordinated oxalate from an adsorption isotherm at pH=3.

  17. Ion exchange of H+, Na+, Mg2+, Ca2+, Mn2+, and Ba2+, on wood pulp

    Science.gov (United States)

    Alan W. Rudie; Alan Ball; Narendra Patel

    2006-01-01

    Ion exchange selectivity coefficients were measured for the partition of metals between solution and pulp fibers. The method accurately models the ion exchange isotherms for all cation pairs evaluated and is accurate up to approximately 0.05 molar concentrations. Selectivity coefficients were determined for calcium and magnesium with each other and with hydrogen....

  18. Efficacy of zoniporide, an Na/H exchange ion inhibitor, for reducing perioperative cardiovascular events in vascular surgery patients.

    Science.gov (United States)

    Fleisher, Lee A; Newman, Mark F; St Aubin, Lisa B; Cropp, Anne B; Billing, C Bill; Bonney, Sharon; Mackey, William C; Poldermans, Don; Corbalan, Roman; Pereira, Adamastor H; Coriat, Pierre

    2005-10-01

    To determine whether a novel Na+/H+ exchange ion inhibitor, zoniporide, is associated with reduced perioperative myocardial ischemic injury in high-risk surgery patients. Randomized double-blind placebo-controlled multidose trial. Multicenter worldwide (105 centers) trial. Patients with known or multiple risk factors for coronary artery disease undergoing noncardiac vascular surgery. Four parallel groups received 1 of 3 doses of zoniporide or placebo, delivered as a 60-minute loading dose immediately before surgery, and followed by a continuous intravenous infusion for up to 7 days. A total of 824 subjects were randomized into the study from 105 centers worldwide. Of these, 784 subjects received study drug infusion in the 3-mg/kg/d, 6-mg/kg/d, and 12-mg/kg/d groups and the placebo group, and 769 satisfied the criteria for the primary efficacy analysis population. This is 68% of the planned sample size of 1125 subjects. Anesthetic management and perioperative cardiac medications were at the discretion of the attending anesthesiologists, surgeons, and cardiologists. The proportion of subjects who experienced the composite endpoint event (death, myocardial infarction, congestive heart failure, arrhythmia) by postsurgical day 30 was 18.5% in the 12-mg/kg/d group, compared with 15.7% in the placebo group, resulting in a relative risk (RR) of 1.17% (95% confidence interval [CI], 0.80-1.72; p = NS) favoring placebo. The proportions in the lower 2 zoniporide dose groups were slightly lower than in the placebo group, although the sample size is inadequate to reach any firm conclusions. The results fail to demonstrate the efficacy of zoniporide in reducing the proportion of patients at high risk undergoing noncardiac vascular surgery who experience a composite cardiovascular endpoint, which led the corporate sponsor to stop enrollment early on the basis of a futility analysis of the chance of demonstrating efficacy with a larger sample size.

  19. Cross-reactivity of acid-sensing ion channel and Na+–H+ exchanger antagonists with nicotinic acetylcholine receptors

    Science.gov (United States)

    Santos-Torres, Julio; Ślimak, Marta A; Auer, Sebastian; Ibañez-Tallon, Inés

    2011-01-01

    Abstract Nicotinic acetylcholine receptors (nAChRs) are widely distributed throughout the mammalian central and peripheral nervous systems, where they contribute to neuronal excitability and synaptic communication. It has been reported that nAChRs are modulated by BK channels and that BK channels, in turn, are inhibited by acid-sensing ion channels (ASICs). Here we investigate the possible functional interaction between these channels in medial habenula (MHb) neurones. We report that selective antagonists of large-conductance calcium-activated potassium channels and ASIC1a channels, paxilline and psalmotoxin 1, respectively, did not induce detectable changes in nicotine-evoked currents. In contrast, the non-selective ASIC and Na+–H+ exchanger (NHE1) antagonists, amiloride and its analogues, suppressed nicotine-evoked responses in MHb neurones of wild-type and ASIC2 null mice, excluding a possible involvement of ASIC2 in the nAChR inhibition by amiloride. Zoniporide, a more selective inhibitor of NHE1, reversibly inhibited α3β4-, α7- and α4-containing (*) nAChRs in Xenopus oocytes and in brain slices, as well as in PS120 cells deficient in NHE1 and virally transduced with nAChRs, suggesting a generalized effect of zoniporide in most neuronal nAChR subtypes. Independently from nAChR antagonism, zoniporide profoundly blocked synaptic transmission onto MHb neurones without affecting glutamatergic and GABA receptors. Taken together, these results indicate that amiloride and zoniporide, which are clinically used to treat hypertension and cardiovascular disease, have an inhibitory effect on neuronal nAChRs when used experimentally at high doses. The possible cross-reactivity of these compounds with nAChRs in vivo will require further investigation. PMID:21911609

  20. Study of electrostatic acceleration of H and D negative ion beams. Application to the 1 MeV SINGAP accelerator

    International Nuclear Information System (INIS)

    Bucalossi, J.

    1998-04-01

    In the framework of the development of a neutral beam injection system for ITER (International Thermonuclear Experimental Reactor), the electrostatic acceleration of negative ion H/D beams up to an energy of 1 MeV has been studied. With the support of 3-D beam trajectory calculations, the limitations of the multi-aperture multi-grid acceleration concept, ITER reference concept, ar shown and the relevance of a new concept, called SINGAP, is demonstrated. In a SINGAP accelerator, beamlets are pre-accelerated with a classical triode multi-apertures system up to ∼ 50 keV. The pre-accelerated beamlets are then merged into a single beam and post-accelerated at high energy through a large SINGle APerture using one SINgle GAP. The optics of one pre-accelerated beamlet has been studied on the INCA triode accelerator at the Ecole Polytechnique. A diagnostic has been developed to measure the emittance of the pre-accelerated beamlet. A diagnostic has been developed to measure the emittance of the pre-accelerated beamlet. Values of ∼ 0.03π.mrad.cm for the effective normalized emittance and ∼ 12 mrad for the minimal beam divergence have been found (Hbeams). Besides, the effects of co-extracted electrons and pressure in the transport region on the beam optics are shown and experiment is compared to beam numerical simulation. On the Cadarache 1 MeV, 100 mA, D- SINGAP accelerator, beams of 1 s pulse were produced at a level of 900 keV (without observing breakdowns between electrodes). SINGAP optics has been investigated using an infrared calorimetric beam profile diagnostic (2-D) and a neutral beam profile diagnostic (1-D). The control of the beam optics is very satisfying: a divergence of ∼ 10 mrad has been measured, and 3-D simulations and experimentation are in good agreement. (author)

  1. Radicals and ions controlling by adjusting the antenna-substrate distance in a-Si:H deposition using a planar ICP for c-Si surface passivation

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, H.P., E-mail: haipzhou@uestc.edu.cn [School of Energy Science and Engineering, University of Electronic Science and Technology of China, 2006 Xiyuan Ave., West High-Tech Zone, Chengdu, Sichuan, 611731 (China); Plasma Sources and Application Center, NIE, and Institute of Advanced Studies, Nanyang Technological University, 637616 (Singapore); Xu, S., E-mail: shuyan.xu@nie.edu.sg [Plasma Sources and Application Center, NIE, and Institute of Advanced Studies, Nanyang Technological University, 637616 (Singapore); Xu, M. [Key Laboratory of Information Materials of Sichuan Province & School of Electrical and Information Engineering, Southwest University for Nationalities, Chengdu, 610041 (China); Xu, L.X.; Wei, D.Y. [Plasma Sources and Application Center, NIE, and Institute of Advanced Studies, Nanyang Technological University, 637616 (Singapore); Xiang, Y. [School of Energy Science and Engineering, University of Electronic Science and Technology of China, 2006 Xiyuan Ave., West High-Tech Zone, Chengdu, Sichuan, 611731 (China); Xiao, S.Q. [Key Laboratory of Advanced Process Control for Light Industry (Ministry of Education), Department of Electronic Engineering, Jiangnan University, Wuxi, 214122 (China)

    2017-02-28

    Highlights: • A planar ICP was used to grow a-Si:H films for c-Si surface passivation. • The direct- and remote-plasma was compared for high-quality c-Si surface passivation. • The remote ICP with controlled plasma species and ion bombardments is preferable for the surface passivation of c-Si. - Abstract: Being a key issue in the research and fabrication of silicon heterojunction (SHJ) solar cells, crystalline silicon (c-Si) surface passivation is theoretically and technologically intricate due to its complicate dependence on plasma characteristics, material properties, and plasma-material interactions. Here amorphous silicon (a-Si:H) grown by a planar inductively coupled plasma (ICP) reactor working under different antenna-substrate distances of d was used for the surface passivation of low-resistivity p-type c-Si. It is found that the microstructures (i.e., the crystallinity, Si-H bonding configuration etc.) and passivation function on c-Si of the deposited a-Si:H were profoundly influenced by the parameter of d, which primarily determines the types of growing precursors of SiH{sub n}/H contributing to the film growth and the interaction between the plasma and growing surface. c-Si surface passivation is analyzed in terms of the d-dependent a-Si:H properties and plasma characteristics. The controlling of radical types and ion bombardment on the growing surface through adjusting parameter d is emphasized.

  2. Two center electron emission in collisions of fast ions with H, and H{sub 2}: Interplay between interference and Compton profile effect

    Energy Technology Data Exchange (ETDEWEB)

    Misra, D. [Tata Institute of Fundamental Research, Colaba, Mumbai 400 005 (India); Kumar, Ajay [Tata Institute of Fundamental Research, Colaba, Mumbai 400 005 (India)]. E-mail: lokesh@tifr.res.in; Kadhane, U.R. [Tata Institute of Fundamental Research, Colaba, Mumbai 400 005 (India); Fainstein, P.D. [Centro Atomico Bariloche, 8400 Bariloche (Argentina); Tribedi, L.C. [Tata Institute of Fundamental Research, Colaba, Mumbai 400 005 (India)

    2006-11-15

    Young type interference effect has been studied in case of particle induced ionization of H{sub 2}. Oscillations are derived by comparing the measured DDCS for H{sub 2} with the calculated DDCS for H. The effect of the Compton profiles of H{sub 2} and H on the interference structure is also studied. A theoretical model based on molecular distorted wave calculation explains the experimental results qualitatively.

  3. Multiple scattering of low energy H{sup +} ions in matter: Approximation of mean energy on the Sigmund and Winterbon model

    Energy Technology Data Exchange (ETDEWEB)

    Mekhtiche, A. [Laboratoire SNIRM, Faculté de Physique, Université des Sciences et de la Technologie Houari Boumediene (USTHB), BP 32 El Alia, Bab Ezzouar, Algiers (Algeria); Faculté des Sciences et de la Technologie, Université Yahia Farès de Médéa (Algeria); Khalal-Kouache, K., E-mail: kkouache@yahoo.fr [Laboratoire SNIRM, Faculté de Physique, Université des Sciences et de la Technologie Houari Boumediene (USTHB), BP 32 El Alia, Bab Ezzouar, Algiers (Algeria)

    2016-09-01

    In this paper, angular distributions of slow H{sup +} ions transmitted through different targets (Al, Ag and Au) are calculated using the model of Sigmund and Winterbon (SW) in the multiple scattering theory. Valdés and Arista (VA) developed a method extending the SW model by including the effect of energy loss in the calculation of angular distributions of transmitted ions. Another method has been proposed for such calculations: one can consider the SW model by using an average value for the energy of the ions inside the target. In this contribution, a new expression is proposed for the mean energy which gives a better agreement with the VA model than the precedent one at low energy. Different potentials have been considered to describe the interaction projectile-target atom in this study and the new expression is found to be independent of the interaction potential.

  4. Potential sputtering of protons from hydrogen- and H sub 2 O-terminated Si(1 0 0) surfaces with slow highly charged ions

    CERN Document Server

    Kuroki, K; Yamazaki, Y

    2003-01-01

    A potential sputtering mechanism of hydrogen has been studied for impacts of slow highly charged Xe sup q sup + ions (<5 keV, q=4-12) on well-defined H-terminated and water-saturated Si(1 0 0) surfaces. It was found that the sputtering yields of protons were proportional to q supgamma (gamma approx 5) for both the Si(1 0 0)2x1-H and Si(1 0 0)1x1-H surfaces, although the absolute yield for the Si(1 0 0)1x1-H surface was 10 times larger than that for the Si(1 0 0)2x1-H surface, i.e. the sputtering efficiency per one H-Si bond for the Si(1 0 0)1x1-H surface is five times larger that for the Si(1 0 0)2x1-H surface. The proton sputtering efficiency from a H-O-Si bond was extracted from measurements of the water-saturated surface, which was approx 8 times larger than the H-Si bond of the Si(1 0 0)2x1-H surface. An effective distance of the proton from its substrate was proposed to be the key parameter to govern the yield, which also influences the energy distributions of sputtered protons. These findings are con...

  5. Effect of a Combination of Low Level Ozone and Metal Ions on Reducing Escherichia coli O157:H7 and Listeria monocytogenes

    Directory of Open Access Journals (Sweden)

    Ok-Hwan Lee

    2013-04-01

    Full Text Available Ozonated water has been used as a strong antimicrobial agent against foodborne pathogens. In this study, the combined effect of low level ozonated water and different added components, including 0.2% starch and metal ions (1 mM CuCl2·2H2O and 0.1 mM AgNO3, on inactivation of Escherichia coli O157:H7 and Listeria monocytogenes was investigated. Treatment with 0.4 ppm ozonated water for 30 min resulted in a maximum log reduction in E. coli O157:H7 and L. monocytogenes compared to initial bacterial counts. The log reductions of bacteria in a starch solution containing ozonated water were slightly higher than those in ozonated water alone. Furthermore, the log reductions of E. coli O157:H7 (2.59 and 4.71 log cfu/mL and L. monocytogenes (2.53 and 4.28 log cfu/mL in a metal ion solution containing 0.2 and 0.4 ppm ozone for 30 min were significantly higher than those of the water and starch added groups (p < 0.05. These results indicate that a combination of ozonated water and metal ions may be useful as a antimicrobial agent.

  6. H+ ion-implantation energy dependence of electronic transport properties in the MeV range in n-type silicon wafers using frequency-domain photocarrier radiometry

    International Nuclear Information System (INIS)

    Wang Chinhua; Mandelis, Andreas; Tolev, Jordan; Burchard, Bernd; Meijer, Jan

    2007-01-01

    Industrial n-type Si wafers (resistivity of 5-10 Ω cm) were H + ion implanted with energies between 0.75 and 2.00 MeV, and the electronic transport properties of the implanted layer (recombination lifetime, carrier diffusion coefficient, and front-surface and implanted-interface recombination velocities s 1 and s 2 ) were studied using photocarrier radiometry (PCR). A quantitative fitting procedure to the diffusing photoexcited free-carrier density wave was introduced using a relatively simple two-layer PCR model in lieu of the more realistic but substantially more complicated three-layer model. The experimental trends in the transport properties of H + -implanted Si layers extracted from the PCR amplitude and phase data as functions of implantation energy corroborate a physical model of the implanted layer in which (a) overlayer damage due to the light H + ions decreases with increased depth of implantation at higher energies (b) the implanted region damage close to the interface is largely decoupled from the overlayer crystallinity, and (c) the concentration of implanted H + ions decreases at higher implantation energies at the interface, thus decreasing the degree of implantation damage at the interface proper

  7. Ionisation and dissociation of water induced by swift multicharged ions; Etude de l'ionisation et de la dissociation d'H{sub 2}O induites par collision avec des ions multicharges rapides

    Energy Technology Data Exchange (ETDEWEB)

    Legendre, S

    2006-02-15

    Ionization and dissociation of water molecules and water clusters induced by 11.7 MeV/A Ni{sup 25+} ions were carried out by imaging techniques. Branching ratios, ionisation cross sections and Kinetic Energy Released distributions have been measured together with fragmentation dynamics studies. Multiple ionization represents approximately 30% of the ionizing events. Double ionization produces in significant way atomic oxygen, considered as a possible precursor of the large production of HO{sub 2} radical in liquid water radiolysis by ions of high Linear Energy Transfer. We evidence a strong selectivity of bond breakage in the case of ion-induced HOD fragmentation. Once the molecule doubly ionized, the breakage of the O-H bond is found 6.5 times more probable than that of the O-D bond. A semi-classical calculation simulating the fragmentation dynamics on the potential energy surface of the ground-state of di-cation H{sub 2}O{sup 2+} makes possible to as well reproduce the preferential nature of the breakage of the O-H bond as the position and the shift of the kinetic energy distributions. First results concerning interaction with water clusters are also reported. Measurements in coincidence are carried out giving access to correlation, with the distributions in energy and angle of the emitted fragments. Mass spectrum points fast intra-cluster proton transfer, leading to the emission of protonated clusters. (author)

  8. Influence of pH on Cr(VI) ions removal from aqueous solutions using carboxymethyl cellulose-based hydrogel as adsorbent

    Science.gov (United States)

    Anah, L.; Astrini, N.

    2017-03-01

    The major problem in heavy metal pollution is that these metals are not biodegradable and accordingly accumulate in the bodies of living organisms, causing dangerous diseases and serious cell disorder. According to World Health Organization (WHO), the long term exposure of Cr(VI) levels of over 0.1 ppm causes respiratory problems, liver and kidney damage, and carcinogenicity.Due to its easy operation and of various cheap adsorbents development, adsorption has been proved to be efficient and most economically attractive technique and feasible to the removal of toxic heavy metal from wastewater. The study aimed to report the removal of Cr(VI) ions from aqueous solutions through adsorption process using carboxymethyl cellulose-graft-poly(acrylic acid) (CMC-g-PAA) hydrogel as adsorbent.Effect of pH was studied to remove hexavalent chromium.Graft copolymerization of poly(acrylic acid) onto carboxymethyl cellulose was carried out in the presence of benzoyl peroxide redox initiator and methylenbisacrylamide as crosslinker agent. Batch experiments were carried out to investigate the effects ofinitial pH.The adsorption of Cr(VI) ions as a function of pH was conducted in the initial pH range of 1 to 8. The results indicated that acidic pH strongly favored the adsorption. The optimum pH for adsorption of Cr(VI) ranged from 1 to 3, and the maximum uptake of Cr(VI) from the solution was 6.53 mg/g at pH 1 and 30°C. FTIR spectroscopy, SEM analyses were performed on the adsorbent before and after Cr(VI) binding. All analyses confirmed the complexation of Cr(VI) ions on the adsorbent.

  9. Hydrothermal self-assembly and supercapacitive behaviors of Co(II) ion-modified graphene aerogels in H{sub 2}SO{sub 4} electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Bao, Qi [Department of Systems Engineering and Engineering Management, City University of Hong Kong, Hong Kong (China); Key Laboratory of Marine Environmental Corrosion and Bio-fouling, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071 (China); Hui, K.N., E-mail: bizhui@pusan.ac.kr [School of Materials Science and Engineering, Pusan National University, San 30 Jangjeon-dong, Geumjeong-gu, Busan 609-735 (Korea, Republic of); Hui, K.S., E-mail: kshui@hanyang.ac.kr [Department of Mechanical Convergence Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Wang, Yi [Key Laboratory of Marine Environmental Corrosion and Bio-fouling, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071 (China); Hong, Xiaoting [Department of Systems Engineering and Engineering Management, City University of Hong Kong, Hong Kong (China)

    2014-08-15

    Highlights: • 3D Co(II) ions modified graphene aerogels were prepared by one-step hydrothermal process. • The aerogel electrodes showed hybrid supercapacitor behaviors. • The aerogel electrodes exhibited high rate capability and long-term cycling stability. - Abstract: Reduced graphene oxide (r-GO) aerogels decorated with divalent cobalt ions were synthesized via a one-pot hydrothermal self-assembly route. The interaction of Co(II) ions with 3D r-GO aerogels was investigated by spectroscopic techniques, including Raman, attenuated total reflectance infrared, and X-ray photoelectron spectroscopies. The excellent electrochemical properties of the aerogels were confirmed by cyclic voltammetry, galvanostatic charge/discharge tests, and electrochemical impedance spectroscopy in an acid electrolyte (1 M H{sub 2}SO{sub 4}). The Co(II) ion-modified r-GO aerogels can be used as high-performance hybrid supercapacitor materials with a specific capacitance of 387.2 F g{sup –1} at 1 A g{sup –1} current density and a good cycling stability without capacity decay over 1000 cycles. The mechanical integrity enhancement of the hybrid r-GO aerogel framework and the improvement in its unique capacitive performance are attributed to the efficient interconnection produced by electro-active Co(II) ions.

  10. The effect of axial ion parameters on the properties of glow discharge polymer in T2B/H2 plasma

    Science.gov (United States)

    Ai, Xing; He, Xiao-Shan; Huang, Jing-Lin; He, Zhi-Bing; Du, Kai; Chen, Guo

    2018-03-01

    Glow discharge polymer (GDP) films were fabricated using plasma-enhanced chemical vapor deposition. The main purpose of this work was to explore the correlations of plasma parameters with the surface morphology and chemical structure of GDP films. The intensities of main positive ions and ion energy as functions of axial distances in T2B/H2 plasma were diagnosed using energy-resolved mass spectrometry. The surface morphology and chemical structure were characterized as functions of axial distances using a scanning electron microscope and Fourier transform infrared spectroscopy, respectively. As the axial distance increases, both the intensities of positive ions and high energy ions decreases, and dissociation weakens while polymerization enhances. This leads to the weakening of the cross-linking structure of GDP films and the formation of dome defects on films. Additionally, high energy ions could introduce a strong etching effect to form etching pits. Therefore, an axial distance of about 20 mm was found to be the optimal plasma parameter to prepare the defect-free GDP films. These results could help one to find the optimal plasma parameters for GDP film deposition.

  11. Molecular dynamics simulation to assess the effect of temperature on diffusion coefficients of different ions and water molecules in C-S-H

    Science.gov (United States)

    Zehtab, B.; Tarighat, A.

    2017-10-01

    Diffusion is a particle transportation process beginning from one point of a system to another through random molecular motion. This process depends on various parameters like temperature, concentration gradient, and particle size. The objective of this article is to assess the variation of diffusion coefficients of water molecules, chloride and sodium ions against different temperatures in calcium silicate hydrates (C-S-H) through molecular dynamics simulation. A uniform sodium chloride solution is modeled between cement hydrate layers with no concentration gradient. In such a solution, temperature could affect diffusion process in a significant manner. The two most important crystalline mineral analogues of C-S-H, tobermorite and jennite, are applied in this simulation. Diffusion coefficients of different ions and water molecules are found in different temperatures. It is revealed that diffusion coefficient is higher at high temperatures. Activation energies of chloride and sodium ions transport in cement hydrates are calculated through Arrhenius law. Output values of diffusion coefficients and activation energies are compared to previous experimental and simulation results in the related literature. A multi-scale analysis is run to estimate the penetration depth of Cl- ions in cement paste through Fick's second law.

  12. Highly selective and sensitive colorimetric determination of Cr3 + ion by 4-amino-5-methyl-4H-1,2,4-triazole-3-thiol functionalized Au nanoparticles

    Science.gov (United States)

    Shahrivari, Shima; Faridbod, Farnoush; Ganjali, Mohammad Reza

    2018-02-01

    In this work, a rapid, selective naked eyes colorimetric chemical probe for the detection of Cr3 + was developed based on functionalization of gold nanoparticles. For this purpose, surface of Au NPs was functionalized using 4-amino-5-methyl-4H-1,2,4-triazole-3-thiol (AMTT). Through colorimetric studies, it was found that in the presence of Cr3 + ions, AMTT-Au NPs instantly aggregated and resulted in a color change of the solution from red to blue. The color change of AMTT-Au NPs due to the aggregation induced by Cr3 + can be seen with even naked eyes and also by UV-Vis spectroscopy with a detection limit of 1.8 μM and 0.1 μM, respectively. AMTT-Au NPs showed excellent selectivity toward Cr3 + compared to other cations tested, including K+, Na+, Cs+, Fe3 +, Ni2 +, Cu2 +, Co2 +, Zn2 +, Ba2 +, Ca2 +, Mg2 +, Cd2 +, Pb2 +, Hg2 + ions and especially all trivalent lanthanide ions. The absorbance ratio (A650/A525) was linear toward Cr3 + concentrations in the range of 0.6-6.1 μM (R2 = 0.996). The best response was achieved over a pH range of 3-5. Furthermore, the proposed colorimetric method based on AMTT-Au NPs was successfully used for Cr3 + ion detection in plasma sample and some water samples.

  13. Ion exchange removal of chromium (iii) from tannery wastes by using a strong acid cation exchange resin amberlite ir-120 h+ and its hybrids

    International Nuclear Information System (INIS)

    Ahmad, T.

    2014-01-01

    A strong acid cation exchange resin Amberlite IR-120 H+ and its hybrids with Mn(OH)/sub 2/, Cu(OH)/sub 2/ and Fe(OH)/sub 3/ are used for the removal of chromium (III) from spent tannery bath. The experimental data give good fits with the Langmuir sorption model. The thermodynamic parameters entropy (delta S), enthalpy (delta H) and free energy (delta G) changes are computed, which reveal that the chromium removal from tannery wastes by ion exchangers is an endothermic, physical sorption and entropically driven process. The rate of sorption is found to increase with the increase of resin dosage, stirring speed and temperature. Different kinetic models such as film diffusion, particle diffusion and Lagergren pseudo first order are used to evaluate the mechanism of the process. It is found that the hybrid ion exchange resins have better removal capacity as compared to the parent ion exchanger. The increase in the removal capacity is found to be in the order of the corresponding PZC values of the hybrid ion exchangers. Further, it is suggested that the higher exchange capacity is the result of Donnan effect and specific adsorption of chromium by the oxides / hydroxides present inside the matrix of the organic cation exchanger. (author)

  14. Asymmetric synthesis of multifunctional cyclopentanes and cyclohexanes via oxycarbenium ion cyclizations of 5-alkoxy- 2(3h)-dihydrofuranones

    NARCIS (Netherlands)

    Geertsema, Edzard M.; Leung, Chiu W.; Oeveren, Arjan van; Meetsma, Auke; Feringa, Bernard

    1995-01-01

    Intramolecular nucleophilic additions to oxycarbenium ions derived from 5-alkoxy-2(3)-dihydrofuranones gave substituted cyclopentanes or cyclohexanes in good yields. Stereoselectivity in these reactions was usually very high, while regioselectivity could be improved using silicon containing

  15. Reduction of tetrakis(4-N-methylpyridyl)porphinecobalt(III) by hexaammineruthenium(II). [Spectral studies of effects of pH and added ions on reduction

    Energy Technology Data Exchange (ETDEWEB)

    Pasternack, R.F.

    1976-03-01

    The reduction of tetrakis(4-N-methylpyridyl)porphinecobalt(III) (Co/sup III/TMpyP) by Ru(NH/sub 3/)/sub 6//sup 2 +/ has been studied as a function of pH and added anions. In the range 2 x 10/sup -5/ < or = (H/sup +/) < or = 0.50 M, the reactions are pH independent and the catalytic effects of chloride and thiocyanate ions are quite modest; rate constants (M/sup -1/ s/sup -1/, 25/sup 0/C) in sulfonate media containing chloride and thiocyanate are given by 1.2 x 10/sup 5/ + 3.3 x 10/sup 5/(Cl/sup -/) + 6.6 x 10/sup 5/(SCN/sup -/). A more pronounced influence on rate occurs when thiocyanate or azide ions are bonded directly to the cobalt site. The rate constants for the Ru(NH/sub 3/)/sub 6//sup 2 +/ reduction of CoP(H/sub 2/O)(SCN)/sup 4 +/ is 10 times larger and that for CoP(H/sub 2/O)(N/sub 3/)/sup 4 +/ is 20 times smaller than that for CoP(H/sub 2/O)/sub 2//sup 5 +/ in a similar medium. (auth)

  16. Ion induced dipole clusters H(n)- (3 ≤ n-odd ≤ 13): density functional theory calculations of structure and energy.

    Science.gov (United States)

    Huang, Lulu; Matta, Chérif F; Massa, Lou

    2011-11-17

    We investigate anew the possible equilibrium geometries of ion induced dipole clusters of hydrogen molecular ions, of molecular formula H(n)(-) (3 ≤ n-odd ≤ 13). Our previous publications [Sapse, A. M.; et al. Nature 1979, 278, 332; Rayez, J. C.; et al., J. Chem. Phys. 1981, 75, 5393] indicated these molecules would have a shallow minimum and adopt symmetrical geometries that accord with the valence shell electron pair repulsion (VSEPR) rules for geometries defined by electron pairs surrounding a central point of attraction. These earlier calculations were all based upon Hartree-Fock (HF) calculations with a fairly small basis of atomic functions, except for the H3(-) ion for which configuration interaction (CI) calculations were carried out. A related paper [Hirao, K.; et al., Chem. Phys. 1983, 80, 237] carried out similar calculations on the same clusters, finding geometries similar to our earlier calculations. However, although that paper argued that the stabilization energy of negative ion clusters H(n)(-) is small, vibration frequencies for the whole set of clusters was not reported, and so a definitive assertion of a true equilibrium was not present. In this paper we recalculate the energetics of the ion induced dipole clusters using density function theory (DFT) B3LYP method calculations in a basis of functions (6-311++G(d,p)). By calculating the vibration frequencies of the VSEPR geometries, we prove that in general they are not true minima because not all the resulting frequencies correspond to real values. By searching the energy surface of the B3LYP calculations, we find the true minimum geometries, which are surprising configurations and are perhaps counterintuitive. We calculate the total energy and binding energy of the new geometries. We also calculate the bond paths associated with the quantum theory of atoms in molecules (QTAIM). The B3LYP/6-311++G(d,p) results, for each molecule, deliver bond paths that radiate between each polarized H2

  17. [(3)H]chlorpromazine photolabeling of the torpedo nicotinic acetylcholine receptor identifies two state-dependent binding sites in the ion channel.

    Science.gov (United States)

    Chiara, David C; Hamouda, Ayman K; Ziebell, Michael R; Mejia, Luis A; Garcia, Galo; Cohen, Jonathan B

    2009-10-27

    Chlorpromazine (CPZ), a potent nicotinic acetylcholine receptor (nAChR) noncompetitive antagonist, binds with higher affinity in the ion channel in the desensitized state than in the closed channel state and with low affinity to additional sites in nAChR-rich membranes. For nAChR equilibrated with agonist, we confirm previous reports that [(3)H]CPZ occupies a site near the cytoplasmic end of the M2 ion channel domain, photolabeling positions M2-2, M2-6, and/or M2-9 in each subunit. We find that [(3)H]CPZ also binds at the extracellular end of the channel, photolabeling amino acids at positions M2-16 (alpha,gamma), M2-17 (alpha,beta,delta), and M2-20 (alpha,beta,delta). The photolabeling at the cytoplasmic end of the channel is fully inhibitable by phencyclidine or proadifen, whereas neither drug inhibits [(3)H]CPZ photolabeling at the extracellular end, establishing that positively charged drugs can bind simultaneously at the cytoplasmic and extracellular ends of the ion channel. [(3)H]CPZ photolabeling is not detected in the transmembrane domain outside the ion channel, but it photolabels alphaMet-386 and alphaSer-393 in the cytoplasmic alphaMA helix. In the nAChR equilibrated with alpha-bungarotoxin to stabilize the nAChR in a closed state, [(3)H]CPZ photolabels amino acids at M2-5 (alpha), M2-6 (alpha,beta,delta), and M2-9 (beta,delta), with no labeling at M2-2. These results provide novel information about the modes of drug binding within the nAChR ion channel and indicate that within the nAChR transmembrane domain, the binding of cationic aromatic amine antagonists can be restricted to the ion channel domain, in contrast to the uncharged, allosteric potentiators and inhibitors that also bind within the delta subunit helix bundle and at subunit interfaces.

  18. Annual report 1990 of the Heavy Ion Physics Department of Hahn-Meitner-Institut Berlin GmbH

    International Nuclear Information System (INIS)

    Eichler, J.; Oertzen, W. von; Lindenberger, H.; Homeyer, H.; Michaelsen, R.

    1991-05-01

    The efficiency of the VICKSI accelerator has again been enhanced by experiments with new ion beams using the isotopes C-14, Fe-54, Se-82, and I-127. Nuclear physics research work investigated hot nuclei, nuclear structures and reaction mechanisms. The research team in solid state physics studied selected problems in connection with heavy ion-solid interactions, deep implantation processes and thin-film structures. There is a complete survey of the scientific publications and lectures. (DG) [de

  19. Influence of the pH on molecular hydrogen primary yields in He{sup 2+} ion tracks in liquid water. A Monte Carlo study

    Energy Technology Data Exchange (ETDEWEB)

    Cobut, Vincent [Departement de Chimie, Universite de Cergy-Pontoise, 5 Mail Gay-Lussac, Neuville/Oise, 95031 Cergy-Pontoise Cedex (France)]. E-mail: vincent.cobut@chim.u-cergy.fr; Corbel, Catherine [CEA-Saclay, DSM/DRECAM/SCM/Laboratoire de Radiolyse, Bat. 546, Piece 5, 91191 Gif-sur-Yvette Cedex (France); Patau, Jean Paul [Faculte de Pharmacie, Universite Paul-Sabatier, 35 chemin des Maraichers, 31062 Toulouse Cedex 4 (France)

    2005-02-01

    Monte Carlo calculations are performed to investigate how the acidity of aqueous solutions at room temperature affects the molecular hydrogen (H{sub 2}) yield as a function of time in 20 MeV-He{sup 2+} ion track segments. For pH values varying from 1 to 13, the time dependence of the calculated yields is nearly independent of pH in the time range 10{sup -12}-10{sup -8} s and only weakly dependent in the time range 10{sup -8}-10{sup -6} s. To understand this behaviour, the kinetic mechanisms governing H{sub 2} formation are examined as a function of time. It is found that the main reactions responsible for the H{sub 2} yield as a function of time are strongly pH-dependent at low and high pH values. The pH-dependences of the reaction yields are however such that the variations in the yields compensate each other. This is why the time dependence of the H{sub 2} yield is only weakly pH-dependent.

  20. Application of Taguchi Method to the Optimization of a-C:H Coatings Deposited Using Ion Beam Assisted Physical Vapor Deposition

    Directory of Open Access Journals (Sweden)

    W. H. Kao

    2015-02-01

    Full Text Available The Taguchi design method is used to optimize the adhesion, hardness, and wear resistance properties of a-C:H coatings deposited on AISI M2 steel substrates using the ion beam assisted physical vapor deposition method. The adhesion strength of the coatings is evaluated by means of scratch tests, while the hardness is measured using a nanoindentation tester. Finally, the wear resistance is evaluated by performing cyclic ball-on-disc wear tests. The Taguchi experimental results show that the optimal deposition parameters are as follows: a substrate bias voltage of 90 V, an ion beam voltage of 1 kV, an acetylene flow rate of 21 sccm, and a working distance of 7 cm. Given these optimal processing conditions, the a-C:H coating has a critical load of 99.8 N, a hardness of 25.5 GPa, and a wear rate of 0.4 × 10−6 mm3/Nm.

  1. Electrical isolation, thermal stability and rf loss in a multilayer GaAs planar doped barrier diode structure bombarded by H+ and Fe+ ions

    Science.gov (United States)

    Vo, V. T.; Koon, K. L.; Hu, Z. R.; Dharmasiri, C. N.; Subramaniam, S. C.; Rezazadeh, A. A.

    2004-04-01

    Electrical isolation in multilayer GaAs planar doped barrier (PDB) diode structures produced by H+ and Fe+ ion implantation were investigated. For an H+ bombardment with a dose of 1×1015cm-2, a sheet resistivity as high as 3×108 Ω/sq and thermal stability up to 400 °C has been achieved. For samples bombarded by Fe+ ions, a similar high sheet resistivity has also been achieved although a longer annealing time (15 min) and a higher annealing temperature (550 °C) were needed. The rf dissipation losses of coplanar waveguide (CPW) "thru" lines fabricated on bombarded multilayer PDBD structure samples were also examined. The measured rf losses were 1.65 dB/cm at 10 GHz and 3 dB/cm at 40 GHz, similar to the values that a CPW line exhibits on a semi-isolating GaAs substrate.

  2. Tribological properties of nc-TiC/a-C:H coatings prepared by magnetron sputtering at low and high ion bombardment of the growing film

    Czech Academy of Sciences Publication Activity Database

    Souček, P.; Schmidtová, T.; Bursíková, V.; Vašina, P.; Pei, Y.; De Hos, J. Th. M.; Caha, O.; Peřina, Vratislav; Mikšová, Romana; Malinský, Petr

    2014-01-01

    Roč. 241, FEB (2014), s. 64-73 ISSN 0257-8972 R&D Projects: GA MŠk(XE) LM2011019; GA ČR(CZ) GD104/09/H080 Institutional support: RVO:61389005 Keywords : nanocomposites * magnetron sputtering * Titanium carbide * ion flux * friction * wear Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders Impact factor: 1.998, year: 2014

  3. Aggregation induced emission enhancement (AIEE) characteristics of quinoline based compound - A versatile fluorescent probe for pH, Fe(III) ion, BSA binding and optical cell imaging

    Science.gov (United States)

    Manikandan, Irulappan; Chang, Chien-Huei; Chen, Chia-Ling; Sathish, Veerasamy; Li, Wen-Shan; Malathi, Mahalingam

    2017-07-01

    Novel benzimidazoquinoline derivative (AVT) was synthesized through a substitution reaction and characterized by various spectral techniques. Analyzing the optical properties of AVT under absorption and emission spectral studies in different environments exclusively with respect to solvents and pH, intriguing characteristics viz. aggregation induced emission enhancement (AIEE) in the THF solvent and 'On-Off' pH sensing were found at neutral pH. Sensing nature of AVT with diverse metal ions and bovine serum albumin (BSA) was also studied. Among the metal ions, Fe3 + ion alone tunes the fluorescence intensity of AVT probe in aqueous medium from ;turn-on; to ;turn-off; through ligand (probe) to metal charge transfer (LMCT) mechanism. The probe AVT in aqueous medium interacts strongly with BSA due to Fluorescence Resonance Energy Transfer (FRET) and the conformational change in BSA was further analyzed using synchronous fluorescence techniques. Docking study of AVT with BSA reveals that the active site of binding is tryptophan residue which is also supported by the experimental results. Interestingly, fluorescent AVT probe in cells was examined through cellular imaging studies using BT-549 and MDA-MB-231 cells. Thus, the single molecule probe based detection of multiple species and stimuli were described.

  4. Measurement of neutral Ti atoms from TiC and Ti targets sputtered by low-energy H+ and Ar+ ions using laser-induced fluorescence

    International Nuclear Information System (INIS)

    Yamada, R.; Bay, H.L.; Schweer, B.

    1984-01-01

    The sputtering of Ti from TiC and also from pure Ti targets for 500 eV H + and Ar + ion irradiation at normal incidence has been investigated by laser-induced fluorescence. The sputtered neutral Ti atoms in the ground state were observed as a function of fluence and target temperature. This technique is shown to be applicable for in-situ sputtering investigations of TiC. Strong fluence dependences of the fluorescence intensities for Ti and TiC targets were observed. These results are discussed from the viewpoint of chemisorption of oxygen on the target surfaces. In the case of H + bombardment, the depleted layer of carbon atoms near the surface of TiC due to chemical sputtering should also be taken into account to explain the fluence dependence of the fluorescence intensity. No significant temperature dependence of the Ti sputtering yield of TiC for Ar + and H + ion bombardment was found in the steady state, and the physical sputtering yield of the Ti component of TiC is about half the Ti yield from a Ti target for Ar + ion bombardment. (orig.)

  5. Observations of different core water cluster ions Y-(H2O)n (Y = O2, HOx, NOx, COx) and magic number in atmospheric pressure negative corona discharge mass spectrometry.

    Science.gov (United States)

    Sekimoto, Kanako; Takayama, Mitsuo

    2011-01-01

    Reliable mass spectrometry data from large water clusters Y(-)(H(2)O)(n) with various negative core ions Y(-) such as O(2)(-), HO(-), HO(2)(-), NO(2)(-), NO(3)(-), NO(3)(-)(HNO(3))(2), CO(3)(-) and HCO(4)(-) have been obtained using atmospheric pressure negative corona discharge mass spectrometry. All the core Y(-) ions observed were ionic species that play a central role in tropospheric ion chemistry. These mass spectra exhibited discontinuities in ion peak intensity at certain size clusters Y(-)(H(2)O)(m) indicating specific thermochemical stability. Thus, Y(-)(H(2)O)(m) may correspond to the magic number or first hydrated shell in the cluster series Y(-)(H(2)O)(n). The high intensity discontinuity at HO(-)(H(2)O)(3) observed was the first mass spectrometric evidence for the specific stability of HO(-)(H(2)O)(3) as the first hydrated shell which Eigen postulated in 1964. The negative ion water clusters Y(-)(H(2)O)(n) observed in the mass spectra are most likely to be formed via core ion formation in the ambient discharge area (760 torr) and the growth of water clusters by adiabatic expansion in the vacuum region of the mass spectrometers (≈1 torr). The detailed mechanism of the formation of the different core water cluster ions Y(-)(H(2)O)(n) is described. Copyright © 2010 John Wiley & Sons, Ltd.

  6. Synthesis, crystal structure and Raman spectrum of K2[(Pt2(HPO44(H2O2] containing (Pt26+ ions

    Directory of Open Access Journals (Sweden)

    2009-03-01

    Full Text Available In the crystal structure of the acid platinum phosphate dipotassium di-μ-hydrogenphosphato-bis[aquaplatinum(III](Pt—Pt, K2[Pt2(HPO44(H2O2], the (Pt26+ dumbbells within the paddle-wheel complex show Pt—Pt distances of 2.4944 (5 and 2.4892 (5 Å. The pottassium ions are seven-fold coordinated by hydrogenphosphate groups. In the crystal, O—H...O hydrogen bonds help to establish the packing. The Raman spectrum was recorded.

  7. Raman and morphology visualization in epitaxial graphene on 4H-SiC by Nitrogen or Argon ion irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Jin-Hua, E-mail: zhaojinhuazjh@gmail.com [School of Science, Shandong Jianzhu University, Jinan 250101 (China); Qin, Xi-Feng; Wang, Feng-Xiang; Fu, Gang [School of Science, Shandong Jianzhu University, Jinan 250101 (China); Wang, Xue-Lin [School of Physics, Key Laboratory of Particle Physics and Particle Irradiation, Ministry of Education, and State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100 (China)

    2015-12-15

    Graphene is a one-atom-thick planar sheet of carbon atoms that are densely packed into a honeycomb crystal lattice and is attracting tremendous interest since being discovered in 2004. Epitaxial growth of graphene on silicon carbide (SiC) is an effective method to obtain high quality layers. In this work, the effects of irradiation on epitaxial SiC/graphene were studied. The samples were irradiated with Nitrogen and Argon ions at an energy of 200 keV and different fluence with 4 × 10{sup 12} ions/cm{sup 2} to 1 × 10{sup 13} ions/cm{sup 2}. The results of Raman measurements indicate that ion beam irradiation causes defects and disorder in the graphene crystal structure, and the level of defects increases with increasing ion fluence. Surface morphology images are obtained by atomic force microscope (AFM). This work is valuable for the potential application of epitaxial graphene on SiC in the field of optoelectronics devices.

  8. Two center Electron Emission in fast Collisions of Bare C and F Ions with He and H{sub 2} and CDW-EIS Mode

    Energy Technology Data Exchange (ETDEWEB)

    Misra, Deepankar [Tata Institute of Fundamental Research, Homi Bhabha Road, Colaba, Mumbai-400 005 (India); Kelkar, A H [Tata Institute of Fundamental Research, Homi Bhabha Road, Colaba, Mumbai-400 005 (India); Fainstein, P D [Centra Atomico Bariloche, 8400 Bariloche (Argentina); Tribedi, Lokesh C [Tata Institute of Fundamental Research, Homi Bhabha Road, Colaba, Mumbai-400 005 (India)

    2007-09-15

    We report the energy and angular distributions of the electron double differential cross sections (DDCS) for two collision systems: 6 MeV/u C{sup 6+} on H{sub 2} and 4 MeV/u F{sup 9+} ions on He. The electrons having energies between 1 and 500 eV are detected at about ten different emission angles between 30{sup 0} and 150{sup 0}. The measured data is compared with the state-of-the art continuum distorted wave-eikonal initial state (CDW-EIS) and the first Born (B1) models. In case of molecular H{sub 2} target a molecular wave function as been used for the calculations of the cross section of H{sub 2}. A comparative study has been presented for the spectral shape for the atomic (He) and molecular (H{sub 2}) target.

  9. Two center Electron Emission in fast Collisions of Bare C and F Ions with He and H2 and CDW-EIS Mode

    Science.gov (United States)

    Misra, Deepankar; Kelkar, A. H.; Fainstein, P. D.; Tribedi, Lokesh C.

    2007-09-01

    We report the energy and angular distributions of the electron double differential cross sections (DDCS) for two collision systems: 6 MeV/u C6+ on H2 and 4 MeV/u F9+ ions on He. The electrons having energies between 1 and 500 eV are detected at about ten different emission angles between 30° and 150°. The measured data is compared with the state-of-the art continuum distorted wave-eikonal initial state (CDW-EIS) and the first Born (B1) models. In case of molecular H2 target a molecular wave function as been used for the calculations of the cross section of H2. A comparative study has been presented for the spectral shape for the atomic (He) and molecular (H2) target.

  10. Atomic Oxygen (ATOX) simulation of Teflon FEP and Kapton H surfaces using a high intensity, low energy, mass selected, ion beam facility

    Science.gov (United States)

    Vered, R.; Grossman, E.; Lempert, G. D.; Lifshitz, Y.

    1994-11-01

    A high intensity (greater than 10(exp 15) ions/sq cm) low energy (down to 5 eV) mass selected ion beam (MSIB) facility was used to study the effects of ATOX on two polymers commonly used for space applications (Kapton H and Teflon FEP). The polymers were exposed to O(+) and Ne(+) fluences on 10(exp 15) - 10(exp 19) ions/sq cm, using 30eV ions. A variety of analytical methods were used to analyze the eroded surfaces including: (1) atomic force microscopy (AFM) for morphology measurements; (2) total mass loss measurements using a microbalance; (3) surface chemical composition using x-ray photoelectron spectroscopy (XPS), and (4) residual gas analysis (RGA) of the released gases during bombardment. The relative significance of the collisional and chemical degradation processes was evaluated by comparing the effects of Ne(+) and O(+) bombardment. For 30 eV ions it was found that the Kapton is eroded via chemical mechanisms while Teflon FEP is eroded via collisional mechanisms. AFM analysis was found very powerful in revealing the evolution of the damage from its initial atomic scale (roughness of approx. 1 nm) to its final microscopic scale (roughness greater than 1 micron). Both the surface morphology and the average roughness of the bombarded surfaces (averaged over 1 micron x 1 micron images by the system's computer) were determined for each sample. For 30 eV a non linear increase of the Kapton roughness with the O(+) fluence was discovered (a slow increase rate for fluences phi less than 5 x 10(exp 17) O(+)/sq cm, and a rapid increase rate for phi greater than 5 x 10(exp 17) O(+)/sq cm). Comparative studies on the same materials exposed to RF and DC oxygen plasmas indicate that the specific details of the erosion depend on the simulation facility emphasizing the advantages of the ion beam facility.

  11. Radiation-induced erosion of titanium alloy surface and hydrogen adsorption under H+ and He+ ion bombardment

    International Nuclear Information System (INIS)

    Guseva, M.I.; Vinogradova, N.K.; Lemke, N.G.; Mansurova, A.N.; Martynenko, Yu.V.; Smirnov, V.N.; Starshin, E.P.; Syshchikov, V.I.; Chelnokov, O.I.; Fefelov, P.A.

    1982-01-01

    Results of studying hydrogen absorption by titanium alloys (Ti-Al-V and Ti-Al-Zr) and the effect of helium ion- and hydrogen ion bombardment on the character and degree of alloy surface erosion are given. The published data on permeability, solubility and diffusion of hydrogen isotopes into metals are systematized in the Appendix. Results of studying tritium permeability and solubility in a number of scantily studied alloys, titanium alloys included, that can be promising construction materials for different thermonuclear reactor units are presented

  12. PSI-ECRIT(S) a hybrid magnetic system with a mirror ratio of 10 for H-like heavy ion production and trapping

    CERN Document Server

    Biri, S; Hitz, D

    1999-01-01

    At the Paul Scherrer Institut ( PSI, Switzerland) an experimental program is started to measure the ground state shift and width of pionic hydrogen. To calibrate the crystal spectrometer X-ray transitions in hydrogen-like heavy ions (e.g. Ar17+) produced by ECR ion sources, are necessary. In PSI a superconducting cyclotron trap magnet originally developed for high energy experiments will be transformed into an ECR Ion Trap (ECRIT). The SC-magnet can deliver more than 4 Tesla magnetic fields with a mirror ratio of 2. A careful calculation showed this mirror ratio can be increased upto 10 and the trap can operate with frequencies between 5 and 20 GHz. To form a closed resonance zone a relatively large open structure (LBL-AECRU-type) NdFeB hexapole will be applied. The first tests will be performed with 6.4 GHz. Later higher frequencies (10 or 14.5 GHz) and the 2-frequency heating (6.4+10, 6.4+14.5 or 10+14.5) are planned to be applied to get enough quantity of H-like heavy ions. Since the main goal of this mach...

  13. Energy loss and straggling of 1–50 keV H, He, C, N, and O ions passing through few layer graphene

    International Nuclear Information System (INIS)

    Allegrini, Frédéric; Bedworth, Peter; Ebert, Robert W.; Fuselier, Stephen A.; Nicolaou, Georgios; Sinton, Steve

    2015-01-01

    Highlights: • Evaluation of graphene foils for space plasma instruments. • Energy loss and straggling of keV ions passing through graphene foils. • Lower energy loss than for ultra-thin carbon foils. • Thickness non-uniformity leads to higher straggling. - Abstract: Graphene could be an alternative to amorphous carbon foils, in particular in space plasma instrumentation. The interaction of ions or neutral atoms with these foils results in different effects: electron emission, charge exchange, angular scattering, and energy straggling. We showed in previous studies that (1) the charge exchange properties are similar for graphene and regular carbon foils, and (2) the scattering at low energies (few keVs) is less for graphene than for one of our thinnest practical carbon foils. In this study, we report measurements of the energy loss and straggling of ∼1–50 keV H, He, C, N, and O ions in graphene. We compare graphene and a carbon foil for hydrogen. We provide simple power law fits to the average energy loss, energy straggling, and skewness of the energy distributions. We find the energy loss for ions transiting through graphene to be reduced compared to thin carbon foils but the energy straggling to be larger, which we attribute to the non-uniformity of the graphene foils used in this study

  14. Evaluation of pH and calcium ion release in capseal I and II and in two other root canal sealers.

    Science.gov (United States)

    Bae, Keun Hyung; Chang, Seok Woo; Bae, Kwang-Shik; Park, Dong Sung

    2011-11-01

    The aim of this study was to compare the pHs and calcium ion releases of newly developed, calcium phosphate-based root canal sealers (Capseal I and II) with those of Sealapex (SA) and Sankin Apatite Root Sealer III (SARS III). Each material (n = 10) was mixed, inserted into polyvinyl chloride (PVC) tubes, and immersed in a vial containing deionized water. The control group consisted of empty PVC tubes (n = 10). The pHs and calcium ion releases were measured by pH meter and ICP-AES (inductively coupled plasma atomic emission spectrometer) at 24 hours and 96 hours, and at 7, 15, and 28 days. The results were analyzed with the Kruskal-Wallis test. Capseal I and II produced pHs and calcium ion releases higher than or equal to those of SA and SARS III (P < .05). Capseal I and II resulted in higher alkalinity and higher calcium ion releases than SA and SARS III. Copyright © 2011 Mosby, Inc. All rights reserved.

  15. A SIFT Study of the Reactions of H2ONO+ Ions with Several Types of Organic Molecules

    Czech Academy of Sciences Publication Activity Database

    Smith, D.; Wang, T.; Španěl, Patrik

    2003-01-01

    Roč. 230, č. 1 (2003), s. 1-9 ISSN 1387-3806 R&D Projects: GA ČR GA202/03/0827 Institutional research plan: CEZ:AV0Z4040901 Keywords : SIFT * nitrosohydronium ions * protonated nitrous acid Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.361, year: 2003

  16. Sorption of Ni(II) on GMZ bentonite: effects of pH, ionic strength, foreign ions, humic acid and temperature.

    Science.gov (United States)

    Yang, Shitong; Li, Jiaxing; Lu, Yi; Chen, Yixue; Wang, Xiangke

    2009-09-01

    Bentonite has been widely studied in nuclear waste management because of its special physicochemical properties. In this work, the sorption of Ni(II) from aqueous solution onto GMZ bentonite as a function of contact time, pH, ionic strength, foreign ions, humic acid (HA) and temperature was investigated under ambient conditions. The results indicated that the pseudo-second-order rate equation simulated the kinetic sorption process well. The sorption of Ni(II) on GMZ bentonite was strongly dependent on pH and on ionic strength. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation and ion exchange with Na(+)/H(+) on GMZ bentonite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. A positive effect of HA on Ni(II) sorption was found at pH8. The Langmuir, Freundlich, and D-R models were used to simulate the sorption isotherms of Ni(II) at three different temperatures: 303.15, 318.15 and 333.15K. The thermodynamic parameters (DeltaH(0), DeltaS(0) and DeltaG(0)) of Ni(II) sorption on GMZ bentonite at the three different temperatures were calculated from the temperature-dependent sorption isotherms. The results indicated that the sorption process of Ni(II) on GMZ bentonite was endothermic and spontaneous. Experimental results indicate that GMZ bentonite is a suitable sorbent for pre-concentration and solidification of Ni(II) from large volume solutions.

  17. Sorption of Ni(II) on GMZ bentonite: Effects of pH, ionic strength, foreign ions, humic acid and temperature

    International Nuclear Information System (INIS)

    Yang Shitong; Li Jiaxing; Lu Yi; Chen Yixue; Wang Xiangke

    2009-01-01

    Bentonite has been widely studied in nuclear waste management because of its special physicochemical properties. In this work, the sorption of Ni(II) from aqueous solution onto GMZ bentonite as a function of contact time, pH, ionic strength, foreign ions, humic acid (HA) and temperature was investigated under ambient conditions. The results indicated that the pseudo-second-order rate equation simulated the kinetic sorption process well. The sorption of Ni(II) on GMZ bentonite was strongly dependent on pH and on ionic strength. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation and ion exchange with Na + /H + on GMZ bentonite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. A positive effect of HA on Ni(II) sorption was found at pH 8. The Langmuir, Freundlich, and D-R models were used to simulate the sorption isotherms of Ni(II) at three different temperatures: 303.15, 318.15 and 333.15 K. The thermodynamic parameters (ΔH 0 , ΔS 0 and ΔG 0 ) of Ni(II) sorption on GMZ bentonite at the three different temperatures were calculated from the temperature-dependent sorption isotherms. The results indicated that the sorption process of Ni(II) on GMZ bentonite was endothermic and spontaneous. Experimental results indicate that GMZ bentonite is a suitable sorbent for pre-concentration and solidification of Ni(II) from large volume solutions.

  18. Effect of pH and complementary ion concentration on nitrate removal using puroliteA400 Resin impregnated Cu in batch system

    Science.gov (United States)

    Turmuzi, M.; Tarigan, Z. N.; Nadapdap, L.; Batubara, F.

    2018-02-01

    The total nitrogen content in water bodies should be below 50 mg NO3 -/L (11.3 mgN/l) World Health Organization (WHO) 2006. The content of nitrogen exceeding the quality standard threshold will cause damage to the aquatic ecosystem and be carcinogenic to humans. The Purolite A-400 resin will be modified with Cu metal by batch method to see the adsorption allowance of nitrate in synthetic liquid waste with nitrate concentration of 50 mg/l. This study will evaluate the effect of pH and complementary ions on the adsorption process. From the result of the research, the second order pseudo model is the most suitable adsorption kinetics model. For the adsorption isotherms the most suitable model is the Freundlich adsorption isotherm model. The optimum pH conditions were at the range of 8.5. The addition of complementary ions sulfate and phosphate did not show any significant change, but sulfate is the most effective complementary ion with a content of 20 mg/l.

  19. Using MDECR-PECVD to study the impact of ion bombardment energy on microstructural properties of μc-Si:H thin film grown from an SiF{sub 4}/H{sub 2} chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Junkang; Florea, Ileana; Bulkin, Pavel V.; Maurice, Jean-Luc; Johnson, Erik V. [LPICM, CNRS, Ecole Polytechnique, Universite Paris Saclay, 91128 Palaiseau (France)

    2016-12-15

    The matrix-distributed electron cyclotron resonance plasma-enhanced chemical vapor deposition (MDECR-PECVD) technique has been shown to achieve high deposition rates for hydrogenated microcrystalline silicon (μc-Si:H) thin film. Due to the fact that plasma is sustained by a microwave discharge, by biasing the substrate holder with additional power supply, one can achieve independent control over the plasma density and the maximum ion bombardment energy (IBE). In this work, we present studies of the impact of IBE on the microstructural properties of the μc-Si:H film deposited by MDECR-PECVD. Insufficient ion bombardment is found to be responsible for the substantial presence of nano-porous regions within the material, resulting in significant post-deposition oxidation. Good agreement between transmission electron microscopy (TEM) Fresnel contrast analysis and the results of infrared absorption and hydrogen effusion measurements for the deposited films suggest that moderate IBE is of vital importance to achieve high quality μc-Si:H. In doing so, denser films with significantly decreased nano-porous regions and better stability are obtained, which is of great interest to optimize the process parameters for solar cell applications. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  20. The role of hERG1 ion channels in epithelial-mesenchymal transition and the capacity of riluzole to reduce cisplatin resistance in colorectal cancer cells.

    Science.gov (United States)

    Fortunato, Angelo

    2017-08-01

    The transition of cells from the epithelial to the mesenchymal state (EMT) plays an important role in tumor progression. EMT allows cells to acquire mobility, stem-like behavior and resistance to apoptosis and drug treatment. These features turn EMT into a central process in tumor biology. Ion channels are attractive targets for the treatment of cancer since they play critical roles in controlling a wide range of physiological processes that are frequently deregulated in cancer. Here, we investigated the role of ether-a-go-go-related 1 (hERG1) ion channels in the EMT of colorectal cancer cells. We studied the epithelial-mesenchymal profile of different colorectal cancer-derived cell lines and the expression of hERG1 potassium channels in these cell lines using real-time PCR. Next, we knocked down hERG1 expression in HCT116 cells using lentivirus mediated RNA interference and characterized the hERG1 silenced cells in vitro and in vivo. Finally, we investigated the capacity of riluzole, an ion channel-modulating drug used in humans to treat amyotrophic lateral sclerosis, to reduce the resistance of the respective colorectal cancer cells to the chemotherapeutic drug cisplatin. We found that of the colorectal cancer-derived cell lines tested, HCT116 showed the highest mesenchymal profile and a high hERG1 expression. Subsequent hERG1 expression knockdown induced a change in cell morphology, which was accompanied by a reduction in the proliferative and tumorigenic capacities of the cells. Notably, we found that hERG1expression knockdown elicited a reversion of the EMT profile in HCT116 cells with a reacquisition of the epithelial-like profile. We also found that riluzole increased the sensitivity of HCT116 cisplatin-resistant cells to cisplatin. Our data indicate that hERG1 plays a role in the EMT of colorectal cancer cells and that its knockdown reduces the proliferative and tumorigenic capacities of these cells. In addition, we conclude that riluzole may be used in

  1. Effects of humidity on the quantitative determination of HCl, NOx, H2S, and NH3 using a three-stage filter pack with ion chromatography analysis

    International Nuclear Information System (INIS)

    Borek, T.T.; Wu, C.F.

    1993-01-01

    Low-level transuranic (TRU) waste to be stored underground at the Waste Isolation Pilot Plant (WIPP) has the potential to generate low levels of reactive gases such as HCl, NO x H 2 S, and NH 3 through radiological, biological, and chemical (corrosion) processes. Because of the low levels of gas expected to be produced (< 1 ppM), a method was developed which includes the simultaneous sampling of gases using chemically treated filter papers and analysis of the extracted ions by ion chromatography. To determine the effects of humidification on the collection and determination of reactive gases, a humidification system was added to the trace gas generator system to produce a relative humidity approximately equal to that in the Humid Test Bin. This humidification system consisted of gas washing bottles filled with saturated brine (NaCl) that has been shown to produce a relative humidity of approximately 75% in the temperature range of 68 degree F to 86 degree

  2. Exploring the atmospheric chemistry of O2SO3- and assessing the maximum turnover number of ion-catalysed H2SO4 formation

    DEFF Research Database (Denmark)

    Bork, Nicolai Christian; Kurtén, T.; Vehkamäki, H.

    2013-01-01

    It has recently been demonstrated that the O2SO3- ion forms in the atmosphere as a natural consequence of ionizing radiation. Here, we present a density functional theory-based study of the reactions of O2SO3- with O-3. The most important reactions are (a) oxidation to O3SO3- and (b) cluster...... molecule, but reaction (b) is in general much more probable. Although we are unable to assess the overall importance of this cycle in the real atmosphere due to the unknown influence of CO2 and NOx, we roughly estimate that ion-induced catalysis may contribute with several percent of H2SO4 levels...

  3. Cloud Point Extraction and Determination of Silver Ion in Real Sample using Bis((1H-benzo[d ]imidazol-2ylmethylsulfane

    Directory of Open Access Journals (Sweden)

    Farshid Ahmadi

    2011-01-01

    Full Text Available Bis((1H-benzo[d]imidazol-2ylmethylsulfane (BHIS was used as a complexing agent in cloud point extraction for the first time and applied for selective pre-concentration of trace amounts of silver. The method is based on the extraction of silver at pH 8.0 by using non-ionic surfactant T-X114 and bis((1H-benzo[d]imidazol-2ylmethylsulfane as a chelating agent. The adopted concentrations for BHIS, Triton X-114 and HNO3, bath temperature, centrifuge rate and time were optimized. Detection limits (3SDb/m of 1.7 along with enrichment factor of 39 for silver ion was achieved. The high efficiency of cloud point extraction to carry out the determination of analytes in complex matrices was demonstrated. The proposed method was successfully applied to the ultra-trace determination of silver in real samples.

  4. Synthesis of MoS2 and MoO2 for their applications in H2 generation and lithium ion batteries: a review

    Directory of Open Access Journals (Sweden)

    Yufei Zhao, Yuxia Zhang, Zhiyu Yang, Yiming Yan and Kening Sun

    2013-01-01

    Full Text Available Scientists increasingly witness the applications of MoS2 and MoO2 in the field of energy conversion and energy storage. On the one hand, MoS2 and MoO2 have been widely utilized as promising catalysts for electrocatalytic or photocatalytic hydrogen evolution in aqueous solution. On the other hand, MoS2 and MoO2 have also been verified as efficient electrode material for lithium ion batteries. In this review, the synthesis, structure and properties of MoS2 and MoO2 are briefly summarized according to their applications for H2 generation and lithium ion batteries. Firstly, we overview the recent advancements in the morphology control of MoS2 and MoO2 and their applications as electrocatalysts for hydrogen evolution reactions. Secondly, we focus on the photo-induced water splitting for H2 generation, in which MoS2 acts as an important co-catalyst when combined with other semiconductor catalysts. The newly reported research results of the significant functions of MoS2 nanocomposites in photo-induced water splitting are presented. Thirdly, we introduce the advantages of MoS2 and MoO2 for their enhanced cyclic performance and high capacity as electrode materials of lithium ion batteries. Recent key achievements in MoS2- and MoO2-based lithium ion batteries are highlighted. Finally, we discuss the future scope and the important challenges emerging from these fascinating materials.

  5. Electrochemical oxidation of acid black 210 dye on the boron-doped diamond electrode in the presence of phosphate ions: Effect of current density, pH, and chloride ions

    International Nuclear Information System (INIS)

    Costa, Carla Regina; Montilla, Francisco; Morallon, Emilia; Olivi, Paulo

    2009-01-01

    The electrochemical oxidation of acid black 210 dye (AB-210) on the boron-doped diamond (BDD) was investigated under different pH conditions. The best performance for the AB-210 oxidation occurred in alkaline phosphate solution. This is probably due to oxidizing agents such as phosphate radicals and peroxodiphosphate ions, which can be electrochemically produced with good yields on the BDD anode, mainly in alkaline solution. Under this condition, the COD (chemical oxygen demand) removal was higher than that obtained from the model proposed by Comninellis. Electrolyses performed in phosphate buffer and in the presence of chloride ions resulted in faster COD and color removals in acid and neutral solutions, but in alkaline phosphate solution, a better performance in terms of TOC removal was obtained in the absence of chloride. Moreover, organochloride compounds were detected in all electrolyses performed in the presence of chloride. The AB-210 electrooxidation on BDD using phosphate as supporting electrolyte proved to be interesting since oxidizing species generated from phosphate ions were able to completely degrade the dye without producing organochloride compounds.

  6. {sup 4}H-SiC neutron sensors based on ion implanted {sup 10}B neutron converter layer

    Energy Technology Data Exchange (ETDEWEB)

    Issa, F.; Ottaviani, L.; Vervisch, V.; Ferone, R.; Palais, O. [Universite Aix-Marseille, Marseille 13397, (France); Szalkai, D.; Klix, A. [Karlsruhe Institute of Technology, Institute of Neutron Physics and Reactor Technology, Karlsruhe 76344, (Germany); Vermeeren, L. [SCK-CEN, B-2400 Mol, (Belgium); Lyoussi, A. [Laboratoire Dosimetrie Capteurs Instrumentation, CEA, Cadarache 13108, (France); Kuznetsov, A. [University of Oslo, NO-0316 Oslo, (Norway); Lazar, M. [AMPERE, UMR 500, INSA de Lyon, 69621 Villeurbanne, (France); Hallen, A. [KTH, Electrum 229, 16440 Kista, (Sweden)

    2015-07-01

    In the framework of the I{sub S}MART project the main aim is to develop an innovative complete radiation detection system based on silicon carbide technology in view to detect neutrons (thermal and fast) and photons for harsh environments. In the present work two geometries have been realized based on ion implantation of boron. In the first geometry, {sup 10}B ions have been implanted into the Al metallic contact to create the neutron converter layer. In the second geometry one single process has been used to realize both the p+-layer and the neutron converter layer. The technological processes followed to fabricate these detectors, with a study of their electrical behavior and their responses under thermal neutron irradiations are addressed in this paper. (authors)

  7. Encapsulation of a (H3O2)- unit in the aromatic core of a calix[6]arene closed by two Zn(II) ions at the small and large rims.

    Science.gov (United States)

    Coquière, David; Marrot, Jérôme; Reinaud, Olivia

    2006-10-01

    The coordination of a first Zn(II) ion to a calix[6]arene presenting three imidazolyl arms at the small rim and three aniline moieties at the large rim allows the binding of a second Zn(II) ion while hosting a (H3O2)- unit in the aromatic cavity.

  8. Exchange of Co(II) Ions in H-BEA Zeolites. Identification of Aluminium Pairs in the Zeolite Framework

    Czech Academy of Sciences Publication Activity Database

    Bortnovsky, Oleg; Sobalík, Zdeněk; Wichterlová, Blanka

    2001-01-01

    Roč. 46, č. 2 (2001), s. 265-275 ISSN 1387-1811 R&D Projects: GA AV ČR IBS4040015; GA MŠk OC D15.20 Institutional research plan: CEZ:AV0Z4040901 Keywords : BEA zeolites * cobalt ion exchange * zeolite framework aluminium Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.497, year: 2001

  9. Reactivity of C2H5+ with Benzene: Formation of Ethylbenzenium Ions and Implications for Titan's Ionospheric Chemistry

    Czech Academy of Sciences Publication Activity Database

    Žabka, Ján; Polášek, Miroslav; Ascenzi, D.; Tosi, P.; Roithová, Jana; Schröder, Detlef

    2009-01-01

    Roč. 113, č. 42 (2009), s. 11153-11160 ISSN 1089-5639 R&D Projects: GA AV ČR IAA400400702; GA ČR GA203/09/1223 Institutional research plan: CEZ:AV0Z40400503; CEZ:AV0Z40550506 Keywords : gas phase * alkylbenzenium ions * molecule reactions Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.899, year: 2009

  10. Tuning a High Transmission Ion Guide to Prevent Gas-Phase Proton Exchange During H/D Exchange MS Analysis

    Science.gov (United States)

    Guttman, Miklos; Wales, Thomas E.; Whittington, Dale; Engen, John R.; Brown, Jeffery M.; Lee, Kelly K.

    2016-04-01

    Hydrogen/deuterium exchange (HDX) mass spectrometry (MS) for protein structural analysis has been adopted for many purposes, including biopharmaceutical development. One of the benefits of examining amide proton exchange by mass spectrometry is that it can readily resolve different exchange regimes, as evidenced by either binomial or bimodal isotope patterns. By careful analysis of the isotope pattern during exchange, more insight can be obtained on protein behavior in solution. However, one must be sure that any observed bimodal isotope patterns are not artifacts of analysis and are reflective of the true behavior in solution. Sample carryover and certain stationary phases are known as potential sources of bimodal artifacts. Here, we describe an additional undocumented source of deuterium loss resulting in artificial bimodal patterns for certain highly charged peptides. We demonstrate that this phenomenon is predominantly due to gas-phase proton exchange between peptides and bulk solvent within the initial stages of high-transmission conjoined ion guides. Minor adjustments of the ion guide settings, as reported here, eliminate the phenomenon without sacrificing signal intensity. Such gas-phase deuterium loss should be appreciated for all HDX-MS studies using such ion optics, even for routine studies not focused on interpreting bimodal spectra.

  11. Retention of alkali ions by hydrated low-pH cements: Mechanism and Na{sup +}/K{sup +} selectivity

    Energy Technology Data Exchange (ETDEWEB)

    Bach, T.T.H.; Chabas, E. [Commissariat à l' Énergie Atomique et aux Énergies Alternatives, DEN/MAR/DTCD/SPDE, BP 17171, 30207 Bagnols-sur-Cèze Cedex (France); Pochard, I., E-mail: isabelle.pochard@u-bourgogne.fr [ICB, UMR 6303 CNRS Université de Bourgogne, 21078 Dijon (France); Cau Dit Coumes, C. [Commissariat à l' Énergie Atomique et aux Énergies Alternatives, DEN/MAR/DTCD/SPDE, BP 17171, 30207 Bagnols-sur-Cèze Cedex (France); Haas, J. [ICB, UMR 6303 CNRS Université de Bourgogne, 21078 Dijon (France); Frizon, F. [Commissariat à l' Énergie Atomique et aux Énergies Alternatives, DEN/MAR/DTCD/SPDE, BP 17171, 30207 Bagnols-sur-Cèze Cedex (France); Nonat, A. [ICB, UMR 6303 CNRS Université de Bourgogne, 21078 Dijon (France)

    2013-09-15

    Low-pH cements, also referred to as low-alkalinity cements, can be designed by replacing significant amounts of Portland cement by pozzolanic materials. Their pore solution is characterized by a pH near 11, and an alkali concentration much lower than that of Portland cement. This work investigates the retention of sodium and potassium by a hydrated low-pH cement comprising 60% Portland cement and 40% silica fume. It is shown that sorption of potassium is higher than that of sodium and mainly results from counterion charge balancing of the C-S-H negative surface charge. To explain the greater retention of potassium compared to sodium, it is postulated that potassium, unlike sodium, may enter the interlayer of C-S-H to compensate the negative charges in the interlayer, in addition to the external surfaces. This assumption is supported by structural characterization of C-S-H using X-ray diffraction.

  12. Total cross-sections for single electron capture from H, He and H2 targets by impact of Be4+ and B5+ ions

    International Nuclear Information System (INIS)

    Busnengo, H.F.; Rivarola, R.D.; Universidad Nacional de Rosario; Rosario Univ. Nacional

    1996-01-01

    Single electron capture from H, He and H 2 targets by impact of Be 4+ and B 5+ projectiles is studied for intermediate and high collision energies. Total cross-sections are calculated using the continuum distorted wave-eikonal final state model. Theoretical results corresponding to capture to selective final bound states and to all final states are presented for impact energies ranging from 50 keV/amu to 3 MeV/amu. A comparison with available experimental data is also shown. (orig.)

  13. He{sup 3+}{sub 2} and HeH{sup 2+} molecular ions in a strong magnetic field: The Lagrange-mesh approach

    Energy Technology Data Exchange (ETDEWEB)

    Olivares Pilón, Horacio, E-mail: holivare@ulb.ac.be [Physique Quantique, CP 165/82, Université Libre de Bruxelles, B 1050 Brussels (Belgium)

    2012-04-09

    Accurate calculations for the ground state of the molecular ions He{sup 3+}{sub 2} and HeH{sup 2+} placed in a strong magnetic field B≳10{sup 2} a.u. (≈2.35×10{sup 11} G) using the Lagrange-mesh method are presented. The Born–Oppenheimer approximation of zero order (infinitely massive centers) and the parallel configuration (molecular axis parallel to the magnetic field) are considered. Total energies are found with 9–10 s.d. The obtained results show that the molecular ions He{sup 3+}{sub 2} and HeH{sup 2+} exist at B>100 a.u. and B>1000 a.u., respectively, as predicted in Turbiner and López Vieyra (2007) while a saddle point in the potential curve appears for the first time at B∼80 a.u. and B∼740 a.u., respectively. -- Highlights: ► Application of the Lagrange-mesh method to two exotic molecular systems. ► He{sup 3+}{sub 2} and HeH{sup 2+} exist at B>100 a.u. and B>1000 a.u., respectively. ► Accurate results for the total energy. ► A saddle point in the potential appears at B∼80 a.u. and B∼740 a.u., respectively.

  14. Dump and Current Measurement of Unstripped H`ions at the Injection from the CERN LINAC4 Into the PS Booster

    CERN Document Server

    Chamizo, R; Goddard, B; Mereghetti, A; Versaci, R; Weterings, W

    2010-01-01

    Linac4 is the new H- linear accelerator under construction at CERN aiming to double the brightness of the beam injected to the CERN PS Booster (PSB) for delivering proton beams to experiments or further CERN accelerators, down to the LHC. The injection system in the PSB is based on the H- charge exchange where the 160 MeV H- beam is converted into an H+ beam by stripping the electrons with a carbon foil. A beam dump located inside a pulsed magnet for the injection bump will intercept the unstripped ions (H0 and H-) and measure the collected charge to detect the relative efficiency and degradation of the stripping foil. The challenge of the dump design is to meet the requirements of a beam dump providing a current measurement and at the same time minimizing the perturbation of the magnetic field of the surrounding pulsed magnet. This paper describes all phases of the dump design and the main issues related to its integration in the line.

  15. Hydrogen loss and its improved retention in hydrogen plasma treated a-SiNx:H films: ERDA study with 100 MeV Ag7+ ions

    Science.gov (United States)

    Bommali, R. K.; Ghosh, S.; Khan, S. A.; Srivastava, P.

    2018-05-01

    Hydrogen loss from a-SiNx:H films under irradiation with 100 MeV Ag7+ ions using elastic recoil detection analysis (ERDA) experiment is reported. The results are explained under the basic assumptions of the molecular recombination model. The ERDA hydrogen concentration profiles are composed of two distinct hydrogen desorption processes, limited by rapid molecular diffusion in the initial stages of irradiation, and as the fluence progresses a slow process limited by diffusion of atomic hydrogen takes over. Which of the aforesaid processes dominates, is determined by the continuously evolving Hydrogen concentration within the films. The first process dominates when the H content is high, and as the H concentration falls below a certain threshold (Hcritical) the irradiation generated H radicals have to diffuse through larger distances before recombining to form H2, thereby significantly bringing down the hydrogen evolution rate. The ERDA measurements were also carried out for films treated with low temperature (300 °C) hydrogen plasma annealing (HPA). The HPA treated films show a clear increase in Hcritical value, thus indicating an improved diffusion of atomic hydrogen, resulting from healing of weak bonds and passivation of dangling bonds. Further, upon HPA films show a significantly higher H concentration relative to the as-deposited films, at advanced fluences. These results indicate the potential of HPA towards improved H retention in a-SiNx:H films. The study distinguishes clearly the presence of two diffusion processes in a-SiNx:H whose diffusion rates differ by an order of magnitude, with atomic hydrogen not being able to diffuse further beyond ∼ 1 nm from the point of its creation.

  16. Bioelectric patterning during oogenesis: stage-specific distribution of membrane potentials, intracellular pH and ion-transport mechanisms in Drosophila ovarian follicles.

    Science.gov (United States)

    Krüger, Julia; Bohrmann, Johannes

    2015-01-16

    Bioelectric phenomena have been found to exert influence on various developmental and regenerative processes. Little is known about their possible functions and the cellular mechanisms by which they might act during Drosophila oogenesis. In developing follicles, characteristic extracellular current patterns and membrane-potential changes in oocyte and nurse cells have been observed that partly depend on the exchange of protons, potassium ions and sodium ions. These bioelectric properties have been supposed to be related to various processes during oogenesis, e. g. pH-regulation, osmoregulation, cell communication, cell migration, cell proliferation, cell death, vitellogenesis and follicle growth. Analysing in detail the spatial distribution and activity of the relevant ion-transport mechanisms is expected to elucidate the roles that bioelectric phenomena play during oogenesis. To obtain an overview of bioelectric patterning along the longitudinal and transversal axes of the developing follicle, the spatial distributions of membrane potentials (Vmem), intracellular pH (pHi) and various membrane-channel proteins were studied systematically using fluorescent indicators, fluorescent inhibitors and antisera. During mid-vitellogenic stages 9 to 10B, characteristic, stage-specific Vmem-patterns in the follicle-cell epithelium as well as anteroposterior pHi-gradients in follicle cells and nurse cells were observed. Corresponding distribution patterns of proton pumps (V-ATPases), voltage-dependent L-type Ca(2+)-channels, amiloride-sensitive Na(+)-channels and Na(+),H(+)-exchangers (NHE) and gap-junction proteins (innexin 3) were detected. In particular, six morphologically distinguishable follicle-cell types are characterized on the bioelectric level by differences concerning Vmem and pHi as well as specific compositions of ion channels and carriers. Striking similarities between Vmem-patterns and activity patterns of voltage-dependent Ca(2+)-channels were found, suggesting

  17. Low-energy collisions between electrons and BeH+: Cross sections and rate coefficients for all the vibrational states of the ion

    Science.gov (United States)

    Niyonzima, S.; Ilie, S.; Pop, N.; Mezei, J. Zs.; Chakrabarti, K.; Morel, V.; Peres, B.; Little, D. A.; Hassouni, K.; Larson, Å.; Orel, A. E.; Benredjem, D.; Bultel, A.; Tennyson, J.; Reiter, D.; Schneider, I. F.

    2017-05-01

    We provide cross sections and Maxwell rate coefficients for reactive collisions of slow electrons with BeH+ ions on all the eighteen vibrational levels (X1Σ+ , vi+ = 0 , 1 , 2 , … , 17) using a Multichannel Quantum Defect Theory (MQDT)-type approach. These data on dissociative recombination, vibrational excitation and vibrational de-excitation are relevant for magnetic confinement fusion edge plasma modeling and spectroscopy, in devices with beryllium based main chamber materials, such as the International Thermonuclear Experimental Reactor (ITER) and the Joint European Torus (JET). Our results are presented in graphical form and as fitted analytical functions, the parameters of which are organized in tables.

  18. Densities and apparent molar volumes of atmospherically important electrolyte solutions. 2. The systems H(+)-HSO4(-)-SO4(2-)-H2O from 0 to 3 mol kg(-1) as a function of temperature and H(+)-NH4(+)-HSO4(-)-SO4)2-)-H2O from 0 to 6 mol kg(-1) at 25 °C using a Pitzer ion interaction model, and NH4HSO4-H2O and (NH4)3H(SO4)2-H2O over the entire concentration range.

    Science.gov (United States)

    Clegg, S L; Wexler, A S

    2011-04-21

    A Pitzer ion interaction model has been applied to the systems H(2)SO(4)-H(2)O (0-3 mol kg(-1), 0-55 °C) and H(2)SO(4)-(NH(4))(2)SO(4)-H(2)O (0-6 mol kg(-1), 25 °C) for the calculation of apparent molar volume and density. The dissociation reaction HSO(4)(-)((aq)) ↔ H(+)((aq)) + SO(4)(2-)((aq)) is treated explicitly. Apparent molar volumes of the SO(4)(2-) ion at infinite dilution were obtained from part 1 of this work, (1) and the value for the bisulfate ion was determined in this study from 0 to 55 °C. In dilute solutions of both systems, the change in the degree of dissociation of the HSO(4)(-) ion with concentration results in much larger variations of the apparent molar volumes of the solutes than for conventional strong (fully dissociated) electrolytes. Densities and apparent molar volumes are tabulated. Apparent molar volumes calculated using the model are combined with other data for the solutes NH(4)HSO(4) and (NH(4))(3)H(SO(4))(2) at 25 °C to obtain apparent molar volumes and densities over the entire concentration range (including solutions supersaturated with respect to the salts).

  19. On the formation of C2H5O2+ ions having the structure of hydroxy-protonated acetic acid

    NARCIS (Netherlands)

    Terlouw, J.K.; Koster, C.G. de; Levsen, K.

    1984-01-01

    Experiments are reported which are best explained in terms of the formation of the long-sought hydroxy-protonated acetic acid, CH3C(O)OH2- This C2 H5O2+ species, generated upon dissociative ionization of 2,4-dihydroxy-2-methylpentane (consecutive losses of CH3. and C3H6), is characterized by a

  20. Dentinal pH changes following electrophoretically activated calcium hydroxide ions in the root canal space of bovine teeth.

    Science.gov (United States)

    Tsesis, Igor; Lin, Shaul; Weiss, Ervin I; Fuss, Zvi

    2005-06-01

    The aim of the study was to evaluate pH changes of external root dentin surface at different depths following electrophoretic activation of calcium hydroxide (CH) in the root canals. For the study, 60 cavities were drilled on three external root surfaces of 20 bovine teeth specimens to obtain remaining dentin thickness (RDT) of 0.3, 0.7 and 1.0 mm. CH paste was inserted in the lumens. In the experimental group (10 specimens) CH paste was electrophoretically activated. Microelectrode was used to measure pH changes in the cavities immediately after placement of CH, following electrophoretical activation, and after 30 days storage. A significant (P pH following electrophoresis was found in all specimens in the experimental group. Cavities with 0.4 mm RDT showed a maximal pH increase to the value of 11.3 +/- 0.4. In the control group no change in pH was observed after 3 min. A similar increase in pH was observed in both groups after 30 days. The pH changes were significantly depended on the RDT (P pH of external root surface within minutes up to 30 days.

  1. Apparent wavelength shifts of H-like ions caused by the spectral fine structure observed in CHS plasmas

    International Nuclear Information System (INIS)

    Nishimura, Shin; Ida, Katsumi

    1998-01-01

    A new charge exchange spectroscopy (CXS) system viewing the plasma from the upside and the downside simultaneously was installed on the Compact Helical System (CHS) to detect the absolute value of Doppler shift due to poloidal rotation velocity ( i ∼ 100 eV) and in the after-glow recombining phase (T i ∼ 30 eV). The apparent Doppler shift is always red-shift regardless the direction of plasma rotation and is explained as the effect of the spectral fine structure of hydrogen-like ions. (author)

  2. Coupling between the protons and PO{sub 4} tetrahedra in H{sup +}-ion-irradiated TlH{sub 2}PO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Han, D. Y. [Korea Basic Science Institute, Seoul (Korea, Republic of); Han, J. H.; Lee, C. E. [Korea University, Seoul (Korea, Republic of); Lee, K. S. [Inje University, Gimhae (Korea, Republic of); Kim, S. H. [Jeju National University, Jeju (Korea, Republic of)

    2012-11-15

    We studied hydrogen-bonded TlH{sub 2}PO{sub 4} (TDP) ferroelectrics treated with proton-beam bombardment. The TDP material was irradiated with a 1-MeV proton beam at a dose of 10{sup 15}/cm{sup 2}. To analyze the local microscopic structure of TDP, we conducted {sup 1}H combined rotation and multiple pulse spectroscopy (CRAMPS), nuclear magnetic resonance (NMR), and high-resolution {sup 31}P NMR measurements. The isotropic chemical shifts of hydrogen and phosphor nuclei exhibited displacive features throughout the antiferroelectric, ferroelastic, and paraelastic phases that were attributed to the interplay of PO{sub 4} lattice deformation and the microscopic hydrogen bond network. The temperature dependence of the isotropic chemical shift σ{sub iso} in {sup 1}H and high resolution {sup 31}P NMR revealed that the electronic charge redistribution was induced by proton-beam irradiation and the material's elastic properties. We examined the proton-lattice relationship in terms of the proton's location in a local double minimum well and the displacive character of the PO{sub 4} lattice.

  3. Removal of aluminum, iron and manganese ions from industrial wastes using granular activated carbon and Amberlite IR-120H

    Directory of Open Access Journals (Sweden)

    Mohamed E. Goher

    2015-01-01

    Full Text Available The removal of aluminum, iron and manganese from some pollution sources that drain into Ismailia Canal has been investigated using two different sorbents; granular activated carbon (GAC and Amberlite IR-120H (AIR-120H. Batch equilibrium experiments showed that the two sorbents have maximum removal efficiency for aluminum and iron pH 5 and 10 min contact time in ambient room temperature, while pH 7 and 30 min were the most appropriate for manganese removal. Dosage of 2 g/l for both GAC and AIR-120H was established to give the maximum removal capacity. At optimum conditions, the removal trend was in order of Al+3 > Fe+2 > Mn+2 with 99.2, 99.02 and 79.05 and 99.55, 99.42 and 96.65% of metal removal with GAC and AIR-120H, respectively. For the three metals, Langmuir and Freundlich isotherms showed higher R2 values, with a slightly better fitting for the Langmuir model. In addition, separation factors (RL and exponent (n values indicated favorable Langmuir (0 < RL < 1 and Freundlich (1 < n < 10 approach. GAC and AIR-120H can be used as excellent alternative, effective and inexpensive materials to remove high amounts of heavy metals from waste water.

  4. The pH-dependent toxicity of basic pharmaceuticals in the green algae Scenedesmus vacuolatus can be explained with a toxicokinetic ion-trapping model

    Energy Technology Data Exchange (ETDEWEB)

    Neuwoehner, Judith [Eawag, Swiss Federal Institute of Aquatic Science and Technology, Uberlandstr. 133, 8600 Duebendorf (Switzerland); Institute of Biogeochemistry and Pollutant Dynamics (IBP), ETH Zuerich, 8092 Zuerich (Switzerland); Escher, Beate I., E-mail: b.escher@uq.edu.au [The University of Queensland, National Research Centre for Environmental Toxicology (Entox), 39 Kessels Road, Brisbane, QLD 4108 (Australia); Eawag, Swiss Federal Institute of Aquatic Science and Technology, Uberlandstr. 133, 8600 Duebendorf (Switzerland)

    2011-01-17

    Several previous studies revealed that pharmaceuticals with aliphatic amine function exhibit a higher toxicity toward algae than toward other aquatic organisms. Here we investigated the pH-dependent toxicity of the five basic pharmaceuticals fluoxetine, its metabolite norfluoxetine, propranolol, lidocaine, and trimipramine. For all of them, the toxicity increased with increasing pH when aqueous effect concentrations were considered. Since these pharmaceuticals contain a basic amine group that is protonated and thus positively charged at physiological pH and because algae are capable of biological homeostasis, i.e., pH inside the algal cell remains virtually independent of variable external pH, the speciation of aliphatic amines can be different inside the algal cell compared to the external medium. Therefore, we hypothesized that the high toxicity of aliphatic amines in algae is a toxicokinetic effect caused by speciation and not a toxicodynamic effect caused by a specific mode of toxic action. This hypothesis also implies that internal effect concentrations are independent on external pH. On this basis we developed a simple toxicokinetic model, which assumes that only the neutral molecule is bioavailable and can pass the plasma membrane. This assumption is likely to be valid at pH values down to two units below the acidity constant (pK{sub a}). For lower pH values a more complex model would have to be evoked that includes, an, albeit smaller, permeability of the charged species. For pH > pK{sub a} - 2, we can safely assume that the outer membrane serves as insulator and that the charged species is formed inside the cell according to the pH in the cytoplasm. Thus this toxicokinetic model is an ion-trapping model. The input parameters of this model are the measured aqueous effect concentrations determined as a function of pH and the membrane-water partitioning, which was modelled by the liposome-water partition coefficients of the neutral and cationic species. They

  5. The pH-dependent toxicity of basic pharmaceuticals in the green algae Scenedesmus vacuolatus can be explained with a toxicokinetic ion-trapping model.

    Science.gov (United States)

    Neuwoehner, Judith; Escher, Beate I

    2011-01-17

    Several previous studies revealed that pharmaceuticals with aliphatic amine function exhibit a higher toxicity toward algae than toward other aquatic organisms. Here we investigated the pH-dependent toxicity of the five basic pharmaceuticals fluoxetine, its metabolite norfluoxetine, propranolol, lidocaine, and trimipramine. For all of them, the toxicity increased with increasing pH when aqueous effect concentrations were considered. Since these pharmaceuticals contain a basic amine group that is protonated and thus positively charged at physiological pH and because algae are capable of biological homeostasis, i.e., pH inside the algal cell remains virtually independent of variable external pH, the speciation of aliphatic amines can be different inside the algal cell compared to the external medium. Therefore, we hypothesized that the high toxicity of aliphatic amines in algae is a toxicokinetic effect caused by speciation and not a toxicodynamic effect caused by a specific mode of toxic action. This hypothesis also implies that internal effect concentrations are independent on external pH. On this basis we developed a simple toxicokinetic model, which assumes that only the neutral molecule is bioavailable and can pass the plasma membrane. This assumption is likely to be valid at pH values down to two units below the acidity constant (pK(a)). For lower pH values a more complex model would have to be evoked that includes, an, albeit smaller, permeability of the charged species. For pH>pK(a)-2, we can safely assume that the outer membrane serves as insulator and that the charged species is formed inside the cell according to the pH in the cytoplasm. Thus this toxicokinetic model is an ion-trapping model. The input parameters of this model are the measured aqueous effect concentrations determined as a function of pH and the membrane-water partitioning, which was modelled by the liposome-water partition coefficients of the neutral and cationic species. They were deduced

  6. Adenosine 5'-triphosphate formation in Thiobacillus ferrooxidans vesicles by H+ ion gradients comparable to those of environmental conditions.

    OpenAIRE

    Apel, W A; Dugan, P R; Tuttle, J H

    1980-01-01

    Vesicles prepared from iron-grown Thiobacillus ferrooxidans, and subsequently loaded with adenosine 5'-diphosphate and inorganic phosphate, produced adenosine 5'-triphosphate when subjected to H+ gradients comparable to those in the cells' normal environment (i.e., an internal pH in the range of 6.0 to 8.0 with an optimum of 7.0 to 7.8 and an external pH in the range of 2.1 to 4.1 with an optimum of 2.8). Nigericin, dicyclohexylcarbodiimide, and pentachlorophenol decreased adenosine 5'-tripho...

  7. Low Gate Voltage Operated Multi-emitter-dot H+ Ion-Sensitive Gated Lateral Bipolar Junction Transistor

    Science.gov (United States)

    Yuan, Heng; Zhang, Ji-Xing; Zhang, Chen; Zhang, Ning; Xu, Li-Xia; Ding, Ming; Patrick, J. Clarke

    2015-02-01

    A low gate voltage operated multi-emitter-dot gated lateral bipolar junction transistor (BJT) ion sensor is proposed. The proposed device is composed of an arrayed gated lateral BJT, which is driven in the metal-oxide-semiconductor field-effect transistor (MOSFET)-BJT hybrid operation mode. Further, it has multiple emitter dots linked to each other in parallel to improve ionic sensitivity. Using hydrogen ionic solutions as reference solutions, we conduct experiments in which we compare the sensitivity and threshold voltage of the multi-emitter-dot gated lateral BJT with that of the single-emitter-dot gated lateral BJT. The multi-emitter-dot gated lateral BJT not only shows increased sensitivity but, more importantly, the proposed device can be operated under very low gate voltage, whereas the conventional ion-sensitive field-effect transistors cannot. This special characteristic is significant for low power devices and for function devices in which the provision of a gate voltage is difficult.

  8. Young Type Interference Effect on the Forward-Backward Asymmetry Parameter in Electron Emission from H2 Under Fast Ion Impact

    Science.gov (United States)

    Misra, Deepankar; Kelkar, A. H.; Tribedi, Lokesh C.

    2007-09-01

    We have investigated the double differential distribution of electron emission from molecular hydrogen in collisions with fast bare carbon ions in order to investigate the effect of Young type interference on the forward-backward angular asymmetry. The asymmetry parameter, derived from the cross sections for complementary forward and backward angles, shows an oscillatory behaviour as a function of electron velocity which is absent in atomic target such as He. It is shown that the asymmetry parameter which is based on the DDCS of H2 only, can be used as self normalizing way of the obtaining the Young type interference in an inversion symmetric homo-nuclear diatomic molecule like H2. The measured energy and angular distributions as well as the asymmetry parameter are compared with a molecular CDW-EIS (continuum distorted wave-eikonal initial state) model.

  9. Young Type Interference Effect on the Forward-Backward Asymmetry Parameter in Electron Emission from H{sub 2} Under Fast Ion Impact

    Energy Technology Data Exchange (ETDEWEB)

    Misra, Deepankar; Kelkar, A H; Tribedi, Lokesh C [Tata Institute of Fundamental Research, Homi Bhabha Road, Colaba, Mumbai-200 005 (India)

    2007-09-15

    We have investigated the double differential distribution of electron emission from molecular hydrogen in collisions with fast bare carbon ions in order to investigate the effect of Young type interference on the forward-backward angular asymmetry. The asymmetry parameter, derived from the cross sections for complementary forward and backward angles, shows an oscillatory behaviour as a function of electron velocity which is absent in atomic target such as He. It is shown that the asymmetry parameter which is based on the DDCS of H{sub 2} only, can be used as self normalizing way of the obtaining the Young type interference in an inversion symmetric homo-nuclear diatomic molecule like H{sub 2}. The measured energy and angular distributions as well as the asymmetry parameter are compared with a molecular CDW-EIS (continuum distorted wave-eikonal initial state) model.

  10. M-shell ionization of heavy elements by 0.1-1.0 MeV/amu 1,2H and 3,4He ions

    International Nuclear Information System (INIS)

    Pajek, M.; Banas, D.; Braziewicz, J.; Czarnota, M.; Bienkowski, A.; Jaskola, M.; Korman, A.; Trautmann, D.; Lapicki, G.

    2006-01-01

    The M-shell ionization in high-Z atoms by low-energy light 1 1 H, 1 2 H, 2 3 He, and 2 4 He ions have been studied systematically in the energy range 0.1-1.0 MeV/amu in order to verify the available theoretical approaches describing the M-shell ionization by charged particles in asymmetric collisions. The present low-energy data, combined with our earlier results reported for M-shell ionization by hydrogen and helium ions for higher energies, form a systematic experimental basis to test the theoretical predictions of M-shell ionization based on the plane-wave Born approximation (PWBA), the semiclassical approximation (SCA), and the binary-encounter approximation (BEA). In the PWBA based approaches the energy loss (E), Coulomb deflection (C), perturbed stationary state (PSS), and relativistic (R) effects were considered within the ECPSSR theory and its recent modification, called the ECUSAR theory, in which a description of the PSS effect was corrected to account for the united- and separated-atom (USA) electron binding energy limits. In the SCA calculations with relativistic wave functions the binding effect was included only in the limiting cases of separated-atom and united-atom limits. Possible contribution of the electron capture, multiple ionization, and recoil ionization to the M-shell vacancy production, which is dominated for light ions impact by direct single ionization process, are also discussed. The universal scaling of measured M-shell x-ray production and ionization cross sections was investigated in detail. Using the present data the isotopic effect has been studied by comparing the measured M-shell ionization cross-section ratios for equal-velocity hydrogen 1 1 H and 1 2 H as well as helium 2 3 He and 2 4 He isotopes. In addition, the ratios of measured ionization cross sections for 1 2 H and 2 4 He were used to investigate the role of the binding effect. The present results are of practical importance for the application of particle-induced x

  11. Degradation of Organophosphorus Pesticides in Water during UV/H2O2 Treatment: Role of Sulphate and Bicarbonate Ions

    Directory of Open Access Journals (Sweden)

    Am Fadaei

    2012-01-01

    Full Text Available The photodegradation of two organophosphorus pesticides, malathian and diazinon, by sulfate radicals and bicarbonate radicals in aqueous solution were studied. The effect of the operational parameters such as pH, salt concentration, water type, H2O2 concentration and initial concentration of pesticides was studied. Gas chromatography mass spectroscopy (GC–MS was used for analyses of pesticides. When salt effect was studied, it was found that sodium bicarbonate was the most powerful inhibitor used, while sodium sulfate was the weakest one. The highest degradation in UV/H2O2 process for malathion was found in alkaline condition and for diazinon in acidic condition. The photodegradation in all waters used in this work exhibited first order kinetics. Photodegradation rate in distilled water was higher than real water. The degradation of pesticides increased with increasing of H2O2 concentration.

  12. Degradation of Organophosphorus Pesticides in Water during UV/H2O2 Treatment: Role of Sulphate and Bicarbonate Ions

    OpenAIRE

    Fadaei, Am; Dehghani, Mh; Mahvi, Ah; Nasseri, S.; Rastkari, N.; Shayeghi, M.

    2012-01-01

    The photodegradation of two organophosphorus pesticides, malathian and diazinon, by sulfate radicals and bicarbonate radicals in aqueous solution were studied. The effect of the operational parameters such as pH, salt concentration, water type, H2O2 concentration and initial concentration of pesticides was studied. Gas chromatography mass spectroscopy (GC–MS) was used for analyses of pesticides. When salt effect was studied, it was found that sodium bicarbonate was the most powerful inhibitor...

  13. Effect of pH on the release of radionuclides and chelating agents from cement-solidified decontamination ion-exchange resins collected from operating nuclear power stations

    Energy Technology Data Exchange (ETDEWEB)

    McIsaac, C.V.; Akers, D.W.; McConnell, J.W. (EG and G Idaho, Inc., Idaho Falls, ID (USA))

    1991-06-01

    Data are presented on the physical stability and leachability of radionuclides and chelating agents from cement-solidified decontamination ion-exchange resin wastes collected from two operating commercial light water reactors. Small-scale waste--form specimens collected during solidifications performed at the Brunswick Steam Electric Plant Unit 1 and at the James A. FitzPatrick Nuclear Power Station were leach-tested and subjected to compressive strength testing in accordance with the Nuclear Regulatory Commission's Technical Position on Waste Form'' (Revision 1). Samples of untreated resin waste collected from each solidification vessel before the solidification process were analyzed for concentrations of radionuclides, selected transition metals, and chelating agents to determine the quantities of these chemicals in the waste-form specimens. The chelating agents included oxalic, citric, and picolinic acids. In order to determine the effect of leachant chemical composition and pH on the stability and leachability of the waste forms, waste-form specimens were leached in various leachants. Results of this study indicate that differences in pH do not affect releases from cement-solidified decontamination ion-exchange resin waste forms, but that differences in leachant chemistry and the presence of chelating agents may affect the releases of radionuclides and chelating agents. Also, this study indicates that the cumulative releases of radionuclides and chelating agents are similar for waste- form specimens that decomposed and those that retained their general physical form. 36 refs., 60 figs., 28 tabs.

  14. Effect of pH on the release of radionuclides and chelating agents from cement-solidified decontamination ion-exchange resins collected from operating nuclear power stations

    International Nuclear Information System (INIS)

    McIsaac, C.V.; Akers, D.W.; McConnell, J.W.

    1991-06-01

    Data are presented on the physical stability and leachability of radionuclides and chelating agents from cement-solidified decontamination ion-exchange resin wastes collected from two operating commercial light water reactors. Small-scale waste--form specimens collected during solidifications performed at the Brunswick Steam Electric Plant Unit 1 and at the James A. FitzPatrick Nuclear Power Station were leach-tested and subjected to compressive strength testing in accordance with the Nuclear Regulatory Commission's ''Technical Position on Waste Form'' (Revision 1). Samples of untreated resin waste collected from each solidification vessel before the solidification process were analyzed for concentrations of radionuclides, selected transition metals, and chelating agents to determine the quantities of these chemicals in the waste-form specimens. The chelating agents included oxalic, citric, and picolinic acids. In order to determine the effect of leachant chemical composition and pH on the stability and leachability of the waste forms, waste-form specimens were leached in various leachants. Results of this study indicate that differences in pH do not affect releases from cement-solidified decontamination ion-exchange resin waste forms, but that differences in leachant chemistry and the presence of chelating agents may affect the releases of radionuclides and chelating agents. Also, this study indicates that the cumulative releases of radionuclides and chelating agents are similar for waste- form specimens that decomposed and those that retained their general physical form. 36 refs., 60 figs., 28 tabs

  15. Fluorescent sensors based on quinoline-containing styrylcyanine: determination of ferric ions, hydrogen peroxide, and glucose, pH-sensitive properties and bioimaging.

    Science.gov (United States)

    Yang, Xiaodong; Zhao, Peiliang; Qu, Jinqing; Liu, Ruiyuan

    2015-08-01

    A novel styrylcyanine-based fluorescent probe 1 was designed and synthesized via facile methods. Ferric ions quenched the fluorescence of probe 1, whereas the addition of ferrous ions led to only small changes in the fluorescence signal. When hydrogen peroxide was introduced into the solution containing probe 1 and Fe(2+) , Fe(2+) was oxidized to Fe(3+), resulting in the quenching of the fluorescence. The probe 1/Fe(2+) solution fluorescence could also be quenched by H2 O2 released from glucose oxidation by glucose oxidase (GOD), which means that probe 1/Fe(2+) platform could be used to detect glucose. Probe 1 is fluorescent in basic and neutral media but almost non-fluorescent in strong acidic environments. Such behaviour enables it to work as a fluorescent pH sensor in both the solution and solid states and as a chemosensor for detecting volatile organic compounds with high acidity and basicity. Subsequently, the fluorescence microscopic images of probe 1 in live cells and in zebrafish were achieved successfully, suggesting that the probe has good cell membrane permeability and a potential application for imaging in living cells and living organisms. Copyright © 2014 John Wiley & Sons, Ltd.

  16. Electrochemically induced C-H functionalization using bromide ion/2,2,6,6-tetramethylpiperidinyl-N-oxyl dual redox catalysts in a two-phase electrolytic system

    International Nuclear Information System (INIS)

    Li, Chao; Zeng, Cheng-Chu; Hu, Li-Ming; Yang, Feng-Lin; Yoo, Seung Joon; Little, R. Daniel

    2013-01-01

    Highlights: •Electrocatalytic C-H bond functionalization of tetrahydroisoquinolines is reported. •The transformation is mediated by a bromide ion/TEMPO dual redox catalyst system. •The transformation is conducted in a two-phase electrolytic medium. •The mechanism is proposed to proceed via a sequence of oxidation and addition reactions involving water as a nucleophile. •The procedure features wide substrate scope, the use of mild reaction conditions. -- Abstract: The electrochemical oxidative functionalization of benzylic C-H bonds, mediated by a dual bromide ion/2,2,6,6-tetramethylpiperidinyl-N-oxyl (TEMPO) redox catalyst system in a two-phase electrolytic medium, has been explored using cyclic voltammetry (CV) and preparative electrolysis techniques. The results show that electron transfer between TEMPO + and a neutral substrate occurs with an efficiency that depends upon the presence of a base. The preparative scale electrolysis led to the formation of dihydro-isoquinolinones, isochromanone and xanthenone in moderate to excellent yields. On the basis of the CV analysis and preparative electrolysis results, a reaction mechanism is proposed

  17. Effect of pH, fluoride and hydrofluoric acid concentration on ion release from NiTi wires with various coatings.

    Science.gov (United States)

    Katic, Visnja; Curkovic, Lidija; Bosnjak, Magdalena Ujevic; Peros, Kristina; Mandic, Davor; Spalj, Stjepan

    2017-03-31

    Aim was to determine effect of pH, fluoride (F - ) and hydrofluoric acid concentration (HF) on dynamic of nickel (Ni 2+ ) and titanium (Ti 4+ ) ions release. Nickel-titanium wires with untreated surface (NiTi), rhodium (RhNiTi) and nitride (NNiTi) coating were immersed once a week for five min in remineralizing agents, followed by immersion to artificial saliva. Ion release was recorded after 3, 7, 14, 21 and 28 days. Pearson correlations and linear regression were used for statistical analysis. Release of Ni 2+ from NiTi and NNiTi wires correlated highly linearly positively with HF (r=0.948 and 0.940, respectively); for RhNiTi the correlation was lower and negative (r=-0.605; pNiTi (r=0.797) and NNiTi (r=0.788; pNiTi wires better than the pH and F - of the prophylactic agents.

  18. Decapado de un acero inoxidable austenítico mediante mezclas ecológicas basadas en H2O2 - H2SO4 - iones F-

    OpenAIRE

    Narváez, L.; Miranda, J. M.; Ronquillo, A.

    2013-01-01

    This study reports the pickling of 316L stainless steel using mixtures of hydrogen peroxide (H2O2), sulphuric acid (H2SO4) and fluoride ions as hydrofluoric acid (HF), sodium fluoride (NaF) and potassium fluoride (KF). The decomposition of H2O2 in the mixtures was assessed at different temperatures 25 °C to 60 °C, with ferric ion contents from 0 to 40 g/l. According to the results obtained, were established the optimal condition pickling at 20 g/l of ferric ions, 25 °C and p-toluensulphonic a...

  19. 1H NMR study of effects of synergistic anion and metal ion binding on pH titration of the histidinyl side-chain residues of the half-molecules of ovotransferrin

    International Nuclear Information System (INIS)

    Woodworth, R.C.; Butcher, N.D.; Brown, S.A.; Brown-Mason, A.

    1987-01-01

    Separation of ovotransferrin into C-terminal (OTf/2C) and N-terminal (OTf/2N) half-molecules has made possible the resolution of all expected histidinyl C(2)H resonances by proton nuclear magnetic resonance at 250 MHz. The chemical shift of many of the resonances decreases with increasing pH, allowing construction of titration curves, whereas a few resonances fail to titrate. On formation of the Ga/sup III/OTf/2(C 2 O 4 ) ternary complexes, two of the low-field C(2)H resonances in each half-molecule fail to titrate. This behavior implicates the imidazole groups giving rise to these resonances as ligands to the bound metal ion. A third C(2)H resonance in each half-molecule undergoes a marked reduction in pK'/sub a/ on formation of the ternary complex. The imidazole group displaying this resonance is implicated in a proton-relay scheme involved in binding the synergistic anion, oxalate, and a water of hydration on the bound metal ion. The titration curves for the various imidazole resonances have been fit to a four-parameter equation involving estimation of the pK'/sub a/, the limiting chemical shift values, and a Hill constant n. Hill constants of 1, which suggests positive cooperativity in the titration of this residue. The basis for this behavior cannot be rationalized at this time. 13 C NMR studies of [zeta- 13 C]Arg-OTf suggest the Arg side chains may not be intimately involved in formation of the ternary complex

  20. Measurements of the charge exchange and dissociation cross-sections of the H{sub 2}+ ion in a wide energy range; Mesures des sections efficaces d'echange de charge et de dissociation des ions H{sub 2}{sup +} dans une large gamme d'energie (25 - 250 keV)

    Energy Technology Data Exchange (ETDEWEB)

    Guidini, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1962-07-01

    The dissociation, ionisation, and charge exchange cross-sections of molecular hydrogen ions H{sub 2}{sup +} passing through various gases, have been measured as a function of the energy of the ions. The energy range studied was from 25 to 250 keV. The reaction products, analysed by a magnetic field according to their e/m ratio, are collected on scintillation detectors. Two methods have made it possible to separate the various reactions leading to the formation of particles having the same e/m ratio. The first separates the particles according to their energy, the other selects those arriving simultaneously on two different detectors. The results show a large variation in the charge exchange cross-section with the energy of the H{sub 2}{sup +} ions. The variations in the dissociation and ionisation cross-sections are less pronounced. For a given energy, the values of the cross-sections increase with the atomic weight of the target particles. These measurements have been extended to the case of H{sub 2}{sup +} ions passing through a target of charged particles. Preliminary results show an increase in the cross-sections as compared to the preceding case. Finally the scattering of the reaction products has been studied; this scattering is due to the fact that the molecules formed during a reaction are in an unstable state and the nuclei or atoms diverge from each other. (author) [French] Les sections efficaces de dissociation, d'ionisation et d'echange de charge d'ions hydrogene moleculaires H{sub 2}{sup +} traversant differents gaz, ont ete mesurees en fonction de l'energie des ions. La gamme d'energie exploree est comprise entre 25 et 250 keV. Les produits de reactions, analyses suivant leur rapport e/m par un champ magnetique, sont recus sur des detecteurs a scintillations. Deux methodes ont permis de separer les diverses reactions conduisant a la formation de particules ayant meme rapport e/m. L'une classe les particules secondaires en

  1. Structure and reactivity of C7H7+ ions from the decay of tritiated toluenes. Part 1. Reactions of free tolyl ions with methanol in the gas and liquid phases

    International Nuclear Information System (INIS)

    Cacace, F.; Ciranni, G.; Sparapani, C.; Speranza, M.

    1984-01-01

    Labeled tolyl cations from the decay of ring-multitritiated toluene have been allowed to react with methanol in the liquid and the gas phases, at pressures ranging from 6 to 100 torr, yielding methyl tolyl ethers as the major products, without appreciable formation of benzyl methyl ether. The isomeric composition of the products from the gaseous systems depends on the pressure, the percentage of o-tolyl ether increasing at the expense of the para isomer as the methanol pressure is reduced. The results show that the three tolyl ions exist as distinct species in the dilute gas state. When formed in a sufficiently excited state, as from the β decay of a 3 H atom in toluene, they undergo appreciable interconversion, without detectable isomerization to the benzyl cation, at least within the pressure range accessible to the decay technique. 50 references, 1 table

  2. Lateral variations of radiobiological properties of therapeutic fields of 1H, 4He, 12C and 16O ions studied with Geant4 and microdosimetric kinetic model

    Science.gov (United States)

    Dewey, Sophie; Burigo, Lucas; Pshenichnov, Igor; Mishustin, Igor; Bleicher, Marcus

    2017-07-01

    As known, in cancer therapy with ion beams the relative biological effectiveness (RBE) of ions changes in the course of their propagation in tissues. Such changes are caused not only by increasing the linear energy transfer (LET) of beam particles with the penetration depth towards the Bragg peak, but also by nuclear reactions induced by beam nuclei leading to the production of various secondary particles. Although the changes of RBE along the beam axis have been studied quite well, much less attention has been paid to the evolution of RBE in the transverse direction, perpendicular to the beam axis. In order to fill this gap, we simulated radiation fields of 1H, 4He, 12C and 16O nuclei of 20 mm in diameter by means of a Geant4-based Monte Carlo model for heavy-ion therapy connected with the modified microdosimetric kinetic model to describe the response of normal ((α/β)_x-rays=3.8 Gy) and early-responding ((α/β)_x-rays=10 Gy) tissues. Depth and radial distributions of saturation-corrected dose-mean lineal energy, RBE and RBE-weighted dose are investigated for passive beam shaping and active beam scanning. The field of 4He has a small lateral spread as compared with 1H field, and it is characterised by a modest lateral variation of RBE suggesting the use of fixed RBE values across the field transverse cross section at each depth. Reduced uncertainties of RBE on the boundary of a 4He treatment field can be advantageous in a specific case of an organ at risk located in lateral proximity to the target volume. It is found that the lateral distributions of RBE calculated for 12C and 16O fields demonstrate fast variations in the radial direction due to changes of dose and composition of secondary fragments in the field penumbra. Nevertheless, the radiation fields of all four projectiles at radii larger than 20 mm can be characterized by a common RBE value defined by tissue radiosensitivity. These findings can help, in particular, in accessing the transverse

  3. Virtual Protein Purification: A Simple Exercise to Introduce pH as A Parameter That Effects Ion Exchange Chromatography

    Science.gov (United States)

    Clark, Daniel D.; Edwards, Daniel J.

    2018-01-01

    This article describes a simple exercise using a free, easy-to-use, established online program. The exercise helps to reinforce protein purification concepts and introduces undergraduates to pH as a parameter that affects anion-exchange chromatography. The exercise was tested with biochemistry majors at California State University-Chico. Given the…

  4. Charge heterogeneity profiling of monoclonal antibodies using low ionic strength ion-exchange chromatography and well-controlled pH gradients on monolithic columns.

    Science.gov (United States)

    Talebi, Mohammad; Nordborg, Anna; Gaspar, Andras; Lacher, Nathan A; Wang, Qian; He, Xiaoping Z; Haddad, Paul R; Hilder, Emily F

    2013-11-22

    In this work, the suitability of employing shallow pH gradients generated using single component buffer systems as eluents through cation-exchange (CEX) monolithic columns is demonstrated for the high-resolution separation of monoclonal antibody (mAb) charge variants in three different biopharmaceuticals. A useful selection of small molecule buffer species is described that can be used within very narrow pH ranges (typically 1 pH unit) defined by their buffer capacity for producing controlled and smooth pH profiles when used together with porous polymer monoliths. Using very low ionic strength eluents also enabled direct coupling with electrospray ionisation mass spectrometry. The results obtained by the developed pH gradient approach for the separation of closely related antibody species appear to be consistent with those obtained by imaged capillary isoelectric focusing (iCE) in terms of both resolution and separation profile. Both determinants of resolution, i.e., peak compression and peak separation contribute to the gains in resolution, evidently through the Donnan potential effect, which is increased by decreasing the eluent concentration, and also through the way electrostatic charges are distributed on the protein surface. Retention mechanisms based on the trends observed in retention of proteins at pH values higher than the electrophoretic pI are also discussed using applicable theories. Employing monolithic ion-exchangers is shown to enable fast method development, short analysis time, and high sample throughput owing to the accelerated mass transport of the monolithic media. The possibility of short analysis time, typically less than 15 min, and high sample throughput is extremely useful in the assessment of charge-based changes to the mAb products, such as during manufacturing or storage. Copyright © 2013 Elsevier B.V. All rights reserved.

  5. Electronic bond structure of the H2+ ion in a strong magnetic field: A study of the parallel configuration

    International Nuclear Information System (INIS)

    Kappes, U.; Schmelcher, P.

    1995-01-01

    A large number of magnetically dressed states of the hydrogen molecular ion for parallel internuclear and magnetic field axes are investigated. The numerical calculations of the molecular states and potential-energy curves in the fixed-nuclei approximation are based on a recently established and optimized atomic orbital basis set. We study electronic states within the range 0≤|m|≤10 of magnetic quantum numbers and for several field strengths. In particular, we also investigate many excited states within a subspace for fixed magnetic quantum number and parity. In order to understand the influence of the magnetic field on theof excited molecular states, we perform a detailed comparison of the electronic probability distributions and potential-energy curves in the field-free space with those in the presence of a magnetic field. As a major result we observe the existence of two different classes of strongly bound, i.e., stable, magnetically dressed states whose corresponding counterparts in the field-free space exhibit purely repulsive potential-energy curves, i.e., are unstable. Corrections which are going beyond the fixed-nuclei approach, i.e., the coupling of the center of mass to the electronic motion, as well as the mass corrections are investigated in order to ensure the physical validity of our results

  6. Exploring the atmospheric chemistry of O2SO3− and assessing the maximum turnover number of ion-catalysed H2SO4 formation

    Directory of Open Access Journals (Sweden)

    N. Bork

    2013-04-01

    Full Text Available It has recently been demonstrated that the O2SO3− ion forms in the atmosphere as a natural consequence of ionizing radiation. Here, we present a density functional theory-based study of the reactions of O2SO3− with O3. The most important reactions are (a oxidation to O2SO3− and (b cluster decomposition into SO3, O2 and O3−. The former reaction is highly exothermic, and the nascent O2SO3− will rapidly decompose into SO4− and O2. If the origin of O2SO3− is SO2 oxidation by O3−, the latter reaction closes a catalytic cycle wherein SO2 is oxidized to SO3. The relative rate between the two major sinks for O2SO3− is assessed, thereby providing a measure of the maximum turnover number of ion-catalysed SO2 oxidation, i.e. how many SO2 can be oxidized per free electron. The rate ratio between reactions (a and (b is significantly altered by the presence or absence of a single water molecule, but reaction (b is in general much more probable. Although we are unable to assess the overall importance of this cycle in the real atmosphere due to the unknown influence of CO2 and NOx, we roughly estimate that ion-induced catalysis may contribute with several percent of H2SO4 levels in typical CO2-free and low NOx reaction chambers, e.g. the CLOUD chamber at CERN.

  7. Ion temperature measurements of H-, D- and He-plasmas in the TCA tokamak by collective Thomson scattering of D2O laser radiation

    International Nuclear Information System (INIS)

    Behn, R.; Dicken, D.; Hackmann, J.; Salito, S.A.; Siegrist, M.R.

    1989-01-01

    Development of collective Thomson scattering as a method to measure the ion temperature of a tokamak plasma has been successful and encouraging results have been obtained during experiments on TCA in H-, D- and He-plasmas. Using a laser source in the far-infrared spectral region allows scattering angles close to 90 o , which results in excellent spatial resolution. The system installed on the TCA tokamak comprises an optically pumped D 2 O laser emitting 0.5 J in a 1.4 μs pulse on its Raman transition at 385μm. A heterodyne receiver with a Schottky barrier diode mixer has been chosen to detect the scattered radiation and analyze its spectral distribution in 12 channels of 80 MHz. Recent improvements of the mixer and 1st IF-amplifier yielded a system NEP of 2.2·10 -19 W/Hz. As a consequence we have obtained results which allow for the first time to evaluate the ion temperature T i in a single laser shot. (author) 3 figs., 1 tab

  8. Electron and ion angular distributions in resonant dissociative photoionization of H{sub 2} and D{sub 2} using linearly polarized light

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez, Jorge; MartIn, Fernando [Departamento de Quimica C-9, Universidad Autonoma de Madrid, 28049 Madrid (Spain)], E-mail: fernando.martin@uam.es

    2009-04-15

    We have evaluated fully differential electron angular distributions in H{sub 2} and D{sub 2} dissociative photoionization by using linearly polarized light of 20, 27 and 33 eV. At 20 eV, the distributions exhibit simple p-wave patterns, which is the signature of direct ionization through the X{sup 2}{sigma}{sub g}{sup +}(1s{sigma}{sub g}) channel. At 27 eV, where the Q{sub 1} autoionizing states are populated, we observe a similar pattern, except when the molecule is oriented perpendicularly to the polarization direction and the energy of the ejected electron is small. In contrast, at 33 eV, autoionization from the Q{sub 1} and Q{sub 2} states leads to interferences between the X{sup 2}{sigma}{sub g}{sup +}(1s{sigma}{sub g}) and {sup 2}{sigma}{sub u}{sup +}(2p{sigma}{sub u}) ionization channels that result in a strong asymmetry of the electron angular distributions along the molecular axis. This asymmetry changes rapidly with the energy of the ejected electron. Electron angular distributions integrated over all possible molecular orientations or ion angular distributions integrated over electron emission angle show no reminiscence of the above phenomena, but the corresponding asymmetry parameters dramatically change with electron and ion energies in the region of autoionizing states.

  9. Visualisation of γH2AX Foci Caused by Heavy Ion Particle Traversal; Distinction between Core Track versus Non-Track Damage

    Science.gov (United States)

    Nakajima, Nakako Izumi; Brunton, Holly; Watanabe, Ritsuko; Shrikhande, Amruta; Hirayama, Ryoichi; Matsufuji, Naruhiro; Fujimori, Akira; Murakami, Takeshi; Okayasu, Ryuichi; Jeggo, Penny; Shibata, Atsushi

    2013-01-01

    Heavy particle irradiation produces complex DNA double strand breaks (DSBs) which can arise from primary ionisation events within the particle trajectory. Additionally, secondary electrons, termed delta-electrons, which have a range of distributions can create low linear energy transfer (LET) damage within but also distant from the track. DNA damage by delta-electrons distant from the track has not previously been carefully characterised. Using imaging with deconvolution, we show that at 8 hours after exposure to Fe (∼200 keV/µm) ions, γH2AX foci forming at DSBs within the particle track are large and encompass multiple smaller and closely localised foci, which we designate as clustered γH2AX foci. These foci are repaired with slow kinetics by DNA non-homologous end-joining (NHEJ) in G1 phase with the magnitude of complexity diminishing with time. These clustered foci (containing 10 or more individual foci) represent a signature of DSBs caused by high LET heavy particle radiation. We also identified simple γH2AX foci distant from the track, which resemble those arising after X-ray exposure, which we attribute to low LET delta-electron induced DSBs. They are rapidly repaired by NHEJ. Clustered γH2AX foci induced by heavy particle radiation cause prolonged checkpoint arrest compared to simple γH2AX foci following X-irradiation. However, mitotic entry was observed when ∼10 clustered foci remain. Thus, cells can progress into mitosis with multiple clusters of DSBs following the traversal of a heavy particle. PMID:23967070

  10. Visualisation of γH2AX foci caused by heavy ion particle traversal; distinction between core track versus non-track damage.

    Directory of Open Access Journals (Sweden)

    Nakako Izumi Nakajima

    Full Text Available Heavy particle irradiation produces complex DNA double strand breaks (DSBs which can arise from primary ionisation events within the particle trajectory. Additionally, secondary electrons, termed delta-electrons, which have a range of distributions can create low linear energy transfer (LET damage within but also distant from the track. DNA damage by delta-electrons distant from the track has not previously been carefully characterised. Using imaging with deconvolution, we show that at 8 hours after exposure to Fe (∼200 keV/µm ions, γH2AX foci forming at DSBs within the particle track are large and encompass multiple smaller and closely localised foci, which we designate as clustered γH2AX foci. These foci are repaired with slow kinetics by DNA non-homologous end-joining (NHEJ in G1 phase with the magnitude of complexity diminishing with time. These clustered foci (containing 10 or more individual foci represent a signature of DSBs caused by high LET heavy particle radiation. We also identified simple γH2AX foci distant from the track, which resemble those arising after X-ray exposure, which we attribute to low LET delta-electron induced DSBs. They are rapidly repaired by NHEJ. Clustered γH2AX foci induced by heavy particle radiation cause prolonged checkpoint arrest compared to simple γH2AX foci following X-irradiation. However, mitotic entry was observed when ∼10 clustered foci remain. Thus, cells can progress into mitosis with multiple clusters of DSBs following the traversal of a heavy particle.

  11. Mechanistic study of lead desorption during the leaching process of ion-absorbed rare earths: pH effect and the column experiment

    Science.gov (United States)

    Xue, Q.; Tang, J., Sr.; Chen, H.

    2017-12-01

    High concentrations of ammonium sulfate, often used in the in-situ mining process, can result in a decrease of pH in the environment and dissolution of rare earth metals. Ammonium sulfate can also cause desorption of toxic heavy metals, leading to environmental and human health implications. In this study, the desorption behavior and fraction changes of lead in the ion-absorbed rare earth ore were studied using batch desorption experiments and column leaching tests. Results from batch desorption experiments showed that the desorption process of lead included fast and slow stages, and followed an Elovich model well. The desorption rate and the proportion of lead content in the solution to the total lead in the soil were observed to increase with a decrease in the initial pH of the ammonium sulfate solution. The lead in soil included an acid extractable fraction, reducible fraction, oxidizable fraction, and a residual fraction, with the predominant fractions being the reducible and acid extractable fractions. 96% of the extractable fraction in soil were desorbed into solution at pH=3.0, and the content of the reducible fraction was observed to initially increase (when pH>4.0) and then decrease (when pHsoil followed the trend of reducible fraction > oxidizable fraction > acid extractable fraction > residual fraction after the simulating leaching mining process. The change in pH was also found to have a larger influence on the acid extractable and reducible fractions than the other two fractions. The proportion of the extractable fraction being leached was ca. 86%, and the reducible fraction was enriched along the migration direction of the leaching liquid. These results suggest that certain lead fractions may desorb again and contaminate the environment via acid rain, which provides significant information for environmental assessment and remediation after mining process.

  12. Imobilisasi Tembaga (Cu dan Netralisasi Aktivitas Ion Hidrogen (pH pada Limbah Cair Industri Peleburan Emas Dengan Batu Gamping (Limestone

    Directory of Open Access Journals (Sweden)

    Onny Setiani

    2016-01-01

    Full Text Available The objectives of this research were to determine the effectiveness of  limestones in neutralizing hydrogen ion activity (pH, immobilizing cooper (Cu and to implement a waste water treatment process from the gold molten industry using a cost-effective method to prevent the environment contamination from hazardous wastes. Before  implementing technology, a preliminary study was done to determine a simple and cost effective  method to neutralize pH, immobilize and sedimentation of Copper (Cu  using limestones (CaCO3. The results of laboratory examination in preliminary study  showed that limestones may decrease the concentration of Cu from 23,070 mg/L to 0.711 mg/L, TDS from 30,302 mgLl to 18,289 mg/L and neutralize pH from 1.0-3.0 to 7.0. This research demonstrate that limestones may provide a cost effective method to immobilize  Cu and neutralize contaminated wastewater of the gold molten industry. Since the technology  is very simple, it is  suggested  to be used by home scale or  small industry to protect the environment from toxic waste pollution.   Keywords: Immobilizing cooper, lime stone, neutralization, waste water.

  13. Interface between Al2O3 and 4H-SiC investigated by time-of-flight medium energy ion scattering

    Science.gov (United States)

    Linnarsson, M. K.; Hallén, A.; Khartsev, S.; Suvanam, S. S.; Usman, M.

    2017-12-01

    The formation of interfacial oxides during heat treatment of dielectric films on 4H-SiC has been studied. The 4H-SiC surface has been carefully prepared to create a clean and abrupt interface to Al2O3. An amorphous, 3 nm thick, Al2O3 film has been prepared on 4H-SiC by atomic layer deposition and rapid thermal annealing was then performed in N2O ambient at 700 °C and 1100 °C during 1 min. The samples were studied by time-of-flight medium energy ion scattering (ToF-MEIS), with sub-nanometer depth resolution and it is seen that, at both annealing temperatures, a thin SiO x (1  ⩽  x  ⩽  2) is formed at the interface. Our results further indicate that carbon remains in the silicon oxide in samples annealed at 700 °C. Additional electrical capacitance voltage measurements indicate that a large concentration of interface traps is formed at this temperature. After 1100 °C annealing, both MEIS and XRD measurements show that these features disappear, in accordance with electrical data.

  14. Exit angle, energy loss and internuclear distance distributions of H2+ ions dissociated when traversing different materials

    International Nuclear Information System (INIS)

    Garcia-Molina, Rafael; Abril, Isabel; Denton, Cristian D.; Arista, Nestor R.

    2000-01-01

    We have performed computer simulations of the trajectory followed by each proton resulting from the dissociation of H 2 + molecules when traversing a thin solid target. We use the dielectric formalism to describe the forces due to electronic excitations in the medium, and we also consider the Coulomb repulsion between the pair of protons. Nuclear collisions with target nuclei are incorporated through a Monte Carlo code and the effect of the coherent scattering is taken into account by means of an effective force model. The distributions of exit angle, energy loss and internuclear separations of the protons fragments are discussed for the case of amorphous carbon and aluminum targets

  15. Interference effect in electron emission in heavy ion collisions with h2 detected by comparison with the measured electron spectrum from atomic hydrogen.

    Science.gov (United States)

    Misra, Deepankar; Kadhane, U; Singh, Y P; Tribedi, L C; Fainstein, P D; Richard, P

    2004-04-16

    Direct evidence of the interference effect in the electron emission spectra from ionization of molecular hydrogen in collisions with bare C and F ions at relatively low collision energies is presented. Oscillations due to the interference are deduced by comparing the measured double differential cross sections of the electrons emitted from molecular hydrogen to those emitted from atomic hydrogen, rather than using the calculated cross sections for H as in a previous report. We believe these experimental data provide stronger support for the evidence of the interference effect. We show that it is not only a feature of very high energy collisions, but also a feature to be observed in relatively lower energy collisions.

  16. Difference-frequency laser spectroscopy of molecular ions with a hollow-cathode cell: extended analysis of the ν1 band of H2D+

    International Nuclear Information System (INIS)

    Amano, T.

    1985-01-01

    A cooled hollow-cathode cell was used for observation of the infrared spectra of positive ions in the 3-μm region with a difference-frequency laser as a radiation source. About an order-of-magnitude enhancement of the signal intensity was attained, compared with the similar signals obtained with our previous glow-discharge cell. Ten more weaker lines of the ν 1 fundamental band of H 2 D + , which could not be observed in our previous experiment [J. Chem. Phys. 81, 2869 (1984)] were measured. Improved molecular constants were obtained from a least-squares fit including the infrared lines and the two millimeter-and submillimeter-wave lines in the ground state

  17. The removal of toxic metals from liquid effluents by ion exchange resins. Part V: Nickel(II/H+/Dowex C400

    Directory of Open Access Journals (Sweden)

    Francisco José Alguacil

    2017-11-01

    Full Text Available The cationic exchange resin Dowex C400 was used to remove nickel(II from aqueous solutions of different pH values and under various experimental conditions: stirring speed of the aqueous solution/resin system, temperature, resin dosage and aqueous ionic strength. The selectivity of the resin was investigated against the presence of various metals in the aqueous solution, and the removal of nickel(II from aqueous solutions was also compared with results obtained using multiwalled carbon nanotubes or functionalized (carboxylic groups multiwalled carbon nanotubes as adsorbents. According to batch experimental data, best fit of the results is obtained with the Freundlich model, whereas the ion exchange process is best explained by the pseudo-first order model. Experimental data fit well to the moving boundary controlled model. Elution of the nickel(II loaded onto Dowex C400 resin is fully possible using acidic solutions.

  18. Electrochemical improvement of low-temperature petroleum cokes by chemical oxidation with H2O2 for their use as anodes in lithium ion batteries

    International Nuclear Information System (INIS)

    Concheso, A.; Santamaria, R.; Menendez, R.; Jimenez-Mateos, J.M.; Alcantara, R.; Lavela, P.; Tirado, J.L.

    2006-01-01

    The electrochemical performance of non-graphitized petroleum cokes has been improved by mild oxidation using hydrogen peroxide, a procedure used for the first time in these materials. For this purpose, various carbonisation temperatures and H 2 O 2 treatments were tested. For low sulfur content cokes, the aqueous oxidative treatment significantly increases the capacity values above 372 mAh/g during the first cycles. In contrast, cokes with a sulfur content of ca. 5%, did not shown a real improvement. The former results have been interpreted in terms of an effective oxidation of the particles surface, which removes unorganized carbon, where lithium can be irreversibly trapped. Moreover, a stable and less resistive passivating layer grows during the first discharge of lithium, as revealed by impedance spectroscopy. Therefore, chemical procedures, as mild oxidation, open an interesting field of research for the improvement of disordered carbons as anode materials in lithium ion batteries

  19. Stopped-flow studies of carbon dioxide hydration and bicarbonate dehydration in H2O and D2O. Acid-base and metal ion catalysis

    International Nuclear Information System (INIS)

    Pocker, Y.; Bjorkquist, D.W.

    1977-01-01

    The approach to equilibrium between carbon dioxide and bicarbonate has been followed by zero-order kinetics both from direction of CO 2 hydration and HCO 3 - dehydration. The rates are monitored at 25.0 0 C using stopped-flow indicator technique in H 2 O as well as D 2 O. The hydration of CO 2 is subject to catalysis by H 2 O (k 0 = 2.9 x 10 -2 s -1 ) and OH - (k/sub OH - / = 6.0 x 10 3 M -1 s -1 ). The value of 0.63 for the ratio k/sub OH - //k/sub OD - / is consistent with a mechanism utilizing a direct nucleophilic attack of OH - on CO 2 . In reverse direction HCO 3 - dehydration is catalyzed predominantly by H 3 O + (k/sub H 3 O + / 4.1 x 10 4 M -1 s -1 ) and to a much lesser degree by H 2 O (k 0 = 2 x 10 -4 s -1 ). The value of 0.56 for ratio k/sub H 3 O + //kD 3 O + / indicates that HCO 3 - may be protonated either in a preequilibrium step or in a rate-determining dehydration step. Both the hydration of CO 2 and the dehydration of bicarbonate are subject to general catalysis. For CO 2 , dibasic phosphate, a zinc imidazole complex, and a copper imidazole complex all enhanced the rate of hydration with respective rate coefficients of 3 x 10 -1 , 6.0, and 2.5 M -1 s -1 . For bicarbonate, monobasic phosphate catalyzed the rate of dehydration (k/sub H 2 PO 4 - / = 1 x 10 -1 M -1 s -1 ). Additionally in going from an ionic strength of 0.1 to 1.0 there was a negligible salt effect for the water-catalyzed hydration of CO 2 . However, the rate constant for the hydronium ion catalyzed dehydration of HCO 3 - was reduced from 4.1 x 10 4 M -1 s -1 to 2.3 x 10 4 M -1 s -1 for the same change in ionic strength. Finally the rate of CO 2 uptake by the complex Co(NH 3 ) 5 OH 2 3+ was followed spectrophotometrically both in H 2 O and D 2 O to determine the solvent isotope effect for a reaction known to involve a nucleophilic attack of a Co(III)-hydroxo complex on CO 2

  20. Effects of metal ions and pH on ofloxacin sorption to cassava residue-derived biochar.

    Science.gov (United States)

    Huang, Peng; Ge, Chengjun; Feng, Dan; Yu, Huamei; Luo, Jiwei; Li, Jiatong; Strong, P J; Sarmah, Ajit K; Bolan, Nanthi S; Wang, Hailong

    2018-03-01

    In this study, the impacts of various cations, cation strength and pH on ofloxacin (OFL) adsorption to cassava residue-derived biochars were determined. The associated adsorption mechanisms are discussed. The biochars were prepared at pyrolysis temperatures ranging from 350°C to 750°C, and labeled as CW350, CW450, CW550, CW650 and CW750. The Freundlich model provided the best fit to describe the adsorption capacity of OFL and the Freundlich coefficient (logK f ) increased with increasing pyrolysis temperature. The inclusion of Zn 2+ or Al 3+ increased OFL sorption capacities of five biochars, while Cu 2+ reduced sorption to CW450 and CW550. No significant impacts on OFL sorption were observed in the presence of K + and Ca 2+ . The concentration of Ca 2+ affected the adsorption capacity of CW550, but had no significant impact on other biochars. The pH of OFL solution, ranging from 3 to 9, had no significant changes on OFL adsorption by all the tested biochars. Results of FTIR spectra and zeta potential indicated that electrostatic interactions, cationic exchange, metal bridging and micropore filling could be the main sorption mechanism between OFL and biochars. These studies indicated that cassava residue can be converted into biochars that are effective adsorbents for removing OFL from aqueous solution. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Chloride Ion Transport by the E. coli CLC Cl−/H+ Antiporter: A Combined Quantum-Mechanical and Molecular-Mechanical Study

    Directory of Open Access Journals (Sweden)

    Chun-Hung Wang

    2018-03-01

    Full Text Available We performed steered molecular dynamics (SMD and umbrella sampling simulations of Cl− ion migration through the transmembrane domain of a prototypical E. coli CLC Cl−/H+ antiporter by employing combined quantum-mechanical (QM and molecular-mechanical (MM calculations. The SMD simulations revealed interesting conformational changes of the protein. While no large-amplitude motions of the protein were observed during pore opening, the side chain rotation of the protonated external gating residue Glu148 was found to be critical for full access of the channel entrance by Cl−. Moving the anion into the external binding site (Sext induced small-amplitude shifting of the protein backbone at the N-terminal end of helix F. As Cl− traveled through the pore, rigid-body swinging motions of helix R separated it from helix D. Helix R returned to its original position once Cl− exited the channel. Population analysis based on polarized wavefunction from QM/MM calculations discovered significant (up to 20% charge loss for Cl− along the ion translocation pathway inside the pore. The delocalized charge was redistributed onto the pore residues, especially the functional groups containing π bonds (e.g., the Tyr445 side chain, while the charges of the H atoms coordinating Cl− changed almost negligibly. Potentials of mean force computed from umbrella sampling at the QM/MM and MM levels both displayed barriers at the same locations near the pore entrance and exit. However, the QM/MM PMF showed higher barriers (~10 kcal/mol than the MM PMF (~2 kcal/mol. Binding energy calculations indicated that the interactions between Cl− and certain pore residues were overestimated by the semi-empirical PM3 Hamiltonian and underestimated by the CHARMM36 force fields, both of which were employed in the umbrella sampling simulations. In particular, CHARMM36 underestimated binding interactions for the functional groups containing π bonds, missing the stabilizations of

  2. Hacking the thylakoid proton motive force for improved photosynthesis: modulating ion flux rates that control proton motive force partitioning into Δψ and ΔpH.

    Science.gov (United States)

    Davis, Geoffry A; Rutherford, A William; Kramer, David M

    2017-09-26

    There is considerable interest in improving plant productivity by altering the dynamic responses of photosynthesis in tune with natural conditions. This is exemplified by the 'energy-dependent' form of non-photochemical quenching ( q E ), the formation and decay of which can be considerably slower than natural light fluctuations, limiting photochemical yield. In addition, we recently reported that rapidly fluctuating light can produce field recombination-induced photodamage (FRIP), where large spikes in electric field across the thylakoid membrane (Δ ψ ) induce photosystem II recombination reactions that produce damaging singlet oxygen ( 1 O 2 ). Both q E and FRIP are directly linked to the thylakoid proton motive force ( pmf ), and in particular, the slow kinetics of partitioning pmf into its ΔpH and Δ ψ components. Using a series of computational simulations, we explored the possibility of 'hacking' pmf partitioning as a target for improving photosynthesis. Under a range of illumination conditions, increasing the rate of counter-ion fluxes across the thylakoid membrane should lead to more rapid dissipation of Δ ψ and formation of ΔpH. This would result in increased rates for the formation and decay of q E while resulting in a more rapid decline in the amplitudes of Δ ψ -spikes and decreasing 1 O 2 production. These results suggest that ion fluxes may be a viable target for plant breeding or engineering. However, these changes also induce transient, but substantial mismatches in the ATP : NADPH output ratio as well as in the osmotic balance between the lumen and stroma, either of which may explain why evolution has not already accelerated thylakoid ion fluxes. Overall, though the model is simplified, it recapitulates many of the responses seen in vivo , while spotlighting critical aspects of the complex interactions between pmf components and photosynthetic processes. By making the programme available, we hope to enable the community of photosynthesis

  3. Evaluation of the Ca ion release, pH and surface apatite formation of a prototype tricalcium silicate cement.

    Science.gov (United States)

    Yamamoto, S; Han, L; Noiri, Y; Okiji, T

    2017-12-01

    To evaluate the Ca 2+ -releasing, alkalizing and apatite-like surface precipitate-forming abilities of a prototype tricalcium silicate cement, which was mainly composed of synthetically prepared tricalcium silicate and zirconium oxide radiopacifier. The prototype tricalcium silicate cement, white ProRoot MTA (WMTA) and TheraCal LC (a light-cured resin-modified calcium silicate-filled material) were examined. The chemical compositions were analysed with a wavelength-dispersive X-ray spectroscopy electron probe microanalyser with an image observation function (SEM-EPMA). The pH and Ca 2+ concentrations of water in which the set materials had been immersed were measured, and the latter was assessed with the EDTA titration method. The surface precipitates formed on the materials immersed in phosphate-buffered saline (PBS) were analysed with SEM-EPMA and X-ray diffraction (XRD). Kruskal-Wallis tests followed by Mann-Whitney U-test with Bonferroni correction were used for statistical analysis (α = 0.05). The prototype cement contained Ca, Si and Zr as major elemental constituents, whereas it did not contain some metal elements that were detected in the other materials. The Ca 2+ concentrations and pH of the immersion water samples exhibited the following order: WMTA = prototype cement > TheraCal LC (P prototype cement and WMTA. The prototype tricalcium silicate cement exhibited similar Ca 2+ -releasing, alkalizing and apatite-like precipitate-forming abilities to WMTA. The Ca 2+ -releasing, alkalizing and apatite-like precipitate-forming abilities of TheraCal LC were lower than those of the other materials. © 2016 International Endodontic Journal. Published by John Wiley & Sons Ltd.

  4. Influence of pH, competing ions, and salinity on the sorption of strontium and cobalt onto biogenic hydroxyapatite

    Science.gov (United States)

    Handley-Sidhu, Stephanie; Mullan, Thomas K.; Grail, Quentin; Albadarneh, Malek; Ohnuki, Toshihiko; Macaskie, Lynne E.

    2016-03-01

    Anthropogenic radionuclides contaminate a range of environments as a result of nuclear activities, for example, leakage from waste storage tanks/ponds (e.g. Hanford, USA or Sellafield sites, UK) or as a result of large scale nuclear accidents (e.g. Chernobyl, Ukraine or Fukushima, Japan). One of the most widely applied remediation techniques for contaminated waters is the use of sorbent materials (e.g. zeolites and apatites). However, a key problem at nuclear contaminated sites is the remediation of radionuclides from complex chemical environments. In this study, biogenic hydroxyapatite (BHAP) produced by Serratia sp. bacteria was investigated for its potential to remediate surrogate radionuclides (Sr2+ and Co2+) from environmentally relevant waters by varying pH, salinity and the type and concentration of cations present. The sorption capacity of the BHAP for both Sr2+ and Co2+ was higher than for a synthetically produced hydroxyapatite (HAP) in the solutions tested. BHAP also compared favorably against a natural zeolite (as used in industrial decontamination) for Sr2+ and Co2+ uptake from saline waters. Results confirm that hydroxyapatite minerals of high surface area and amorphous calcium phosphate content, typical for biogenic sources, are suitable restoration or reactive barrier materials for the remediation of complex contaminated environments or wastewaters.

  5. Deep reactive ion etching of 4H-SiC via cyclic SF6/O2 segments

    Science.gov (United States)

    Luna, Lunet E.; Tadjer, Marko J.; Anderson, Travis J.; Imhoff, Eugene A.; Hobart, Karl D.; Kub, Fritz J.

    2017-10-01

    Cycles of inductively coupled SF6/O2 plasma with low (9%) and high (90%) oxygen content etch segments are used to produce up to 46.6 µm-deep trenches with 5.5 µm-wide openings in single-crystalline 4H-SiC substrates. The low oxygen content segment serves to etch deep in SiC whereas the high oxygen content segment serves to etch SiC at a slower rate, targeting carbon-rich residues on the surface as the combination of carbon-rich and fluorinated residues impact sidewall profile. The cycles work in concert to etch past 30 µm at an etch rate of ~0.26 µm min-1 near room temperature, while maintaining close to vertical sidewalls, high aspect ratio, and high mask selectivity. In addition, power ramps during the low oxygen content segment is used to produce a 1:1 ratio of mask opening to trench bottom width. The effect of process parameters such as cycle time and backside substrate cooling on etch depth and micromasking of the electroplated nickel etch mask are investigated.

  6. TRANSPORT OF SOLAR WIND H{sup +} AND He{sup ++} IONS ACROSS EARTH’S BOW SHOCK

    Energy Technology Data Exchange (ETDEWEB)

    Parks, G. K.; Lin, N. [Space Sciences Laboratory, University of California, Berkeley, CA (United States); Lee, E. [School of Space Research and Institute of Natural Sciences, Kyung Hee University, Yongin (Korea, Republic of); Fu, S. Y.; Ma, Y. Q. [Institute of Space Science, Peking University, Beijing (China); Kim, H. E.; Hong, J. [School of Space Research, Kyung Hee University, Yongin (Korea, Republic of); Yang, Z. W.; Liu, Y. [Key Laboratory for Space Weather, Chinese Academy of Sciences, Beijing (China); Canu, P. [Plasma Physics Laboratory, Ecole Polytechnique, Paris (France); Dandouras, I.; Rème, H. [IRAP, Paul Sabatier University and CNRS, Toulouse (France); Goldstein, M. L., E-mail: parks@ssl.berkeley.edu [NASA Goddard Space Flight Center, Greenbelt, MD (United States)

    2016-07-10

    We have investigated the dependence of mass, energy, and charge of solar wind (SW) transport across Earth’s bow shock. An examination of 111 crossings during quiet SW in both quasi-perpendicular and quasi-parallel shock regions shows that 64 crossings had various degrees of heating and thermalization of SW. We found 22 crossings where the SW speed was <400 km s{sup −1}. The shock potential of a typical supercritical quasi-perpendicular shock estimated from deceleration of the SW and cutoff energy of electron flat top distribution is ∼50 Volts. We find that the temperatures of H{sup +} and He{sup ++} beams that penetrate the shock can sometimes be nearly the same in the upstream and downstream regions, indicating little or no heating had occurred crossing the bow shock. None of the models predict that the SW can cross the bow shock without heating. Our observations are important constraints for new models of collisionless shocks.

  7. Heavy-ion ERDA and spectroscopic ellipsometry characterization of a SiOC:H layered structure as functional coating on polymeric lenses

    Science.gov (United States)

    Kreissig, U.; Gago, R.; Vinnichenko, M.; Fernández-Hidalgo, P.; Martín-Palma, R. J.; Martínez-Duart, J. M.

    2004-06-01

    In order to improve the optical and mechanical performance of plastic ophthalmic lenses the use of surface coatings is necessary. However, the application of such coatings can be limited by bad adhesion to the substrate. One way to overcome this drawback is the use of a layered structure consisting of an adherent layer, an abrasion resistant hard layer and an antireflective (AR) multilayer (ML) stack. In this work we study the preparation of SiO xC y:H layered coatings to increase the mechanical durability of polymeric substrates and to accommodate gradually an external dielectric SiO 2/TiO 2 AR-ML. The coatings were grown by plasma assisted chemical vapor deposition (PACVD) using a mixture of hexamethyldisiloxane (HMDSO) and O 2. The possibility of producing the whole layered stack by adjusting the HMDSO:O 2 ratio was demonstrated. The composition and elemental profiles of the different layers were measured by ERDA using 35 MeV Cl-ions. A polymeric-like gradient layer could be formed followed by a buffer layer Si 28O 47C 15H 10 with a nearly constant composition. The variation of the elemental composition does not affect significantly the optical properties, which are close to that of SiO 2.

  8. Sensing properties of separative paper-based extended-gate ion-sensitive field-effect transistor for cost effective pH sensor applications

    Science.gov (United States)

    Cho, Won-Ju; Lim, Cheol-Min

    2018-02-01

    In this study, we developed a cost-effective ion-sensing field-effect transistor (FET) with an extended gate (EG) fabricated on a separative paper substrate. The pH sensing characteristics of the paper EG was compared with those of other EGs fabricated on silicon, glass, or polyimide substrates. The fabricated paper-based EGFET exhibited excellent sensitivity close to the Nernst response limit as well as to that of the other substrate-based EGFETs. In addition, we found that all EGFETs, regardless of the substrate, have similar non-ideal behavior, i.e., drift phenomenon and hysteresis width. To investigate the degradation and durability of the paper EG after prolonged use, aging-effect tests were carried out in terms of the hysteresis width and sensitivity over a course of 30 days. As a result, the paper EG maintained stable pH sensing characteristics after 30 days. Therefore, we expect that paper EGFETs can provide a cost-effective sensor platform.

  9. Effect of pH and phosphate on trapping capacity of various heavy metal ions with ferritin reactor in flowing seawater.

    Science.gov (United States)

    Kong, Bo; Huang, He-Qing; Lin, Qing-Mei; Cai, Zong-Wei; Chen, Ping

    2005-08-01

    We describe a protein reactor consisting of native liver ferritin of Dasyatis akajei (DALF) and a dialysis bag. Our goal was to study a ferritin reactor for its capacity to trap various heavy metal ions (M2+) in flowing seawater. The reactor is sensitive and inexpensive and can be operated by nonprofessional technicians. A positive relationship between the number of trapped M2+ with the DALF reactor and its concentration in the flowing seawater was observed. Both the pH in the medium and the phosphate content within the ferritin cavity strongly affected trapping capacity. It was found that the ferritin released its phosphate compound directly with a shift in pH without the need for releasing reagent, which differs from the phosphate release characteristics of horse spleen ferritin, as previously described. This behavior evidently makes the trapping capacity with the ferritin reactor weaken, indicating that this trapping capacity is tightly connected to its phosphate compound. Our study shows that a self-regulation ability of the ferritin shell rather than its phosphate compound plays an important role in controlling the rate and capacity of trapping M2+. The ferritin reactor was constructed to monitor the contamination level of M2+ in flowing seawater. Our preliminary data along with fieldwork indicate that the DALF reactor is an analytical means for effectively monitoring the contamination level of M2+ in flowing seawater.

  10. The 100th anniversary of pH (1909-2009. Negative logarithms for measuring hydrogen ions: are they essential in medicine? Part I

    Directory of Open Access Journals (Sweden)

    Francesco Sgambato

    2013-03-01

    Full Text Available Introduction: It has been 100 years since the concept of pH (1909-2009 was ‘‘invented’’ by the Danish chemist-mathematician Søren Peter Lauritz Sørensen (1868-1939 in the chemistry laboratories of the Carlsberg Brewery in Copenhagen. The anniversary provides an opportunity to examine the crucial importance in human life of acid-base balance. Materials and methods: The authors review the historical process that led to the creation of the pH scale, with citation of passages from the original work of Sørensen published 100 years ago. This is followed by a critical analysis of the debate regarding the use of logarithmstomeasure hydrogen ion concentrations based on data from scientific papers published over the past 50 years (1960-2010. Results and discussion: The authors conclude that the concept of acid-base balance can be approached and taught in a simpler, more exciting, and even pleasant fashion without using the infamous and abstruse Henderson-Hasselbalch equation. The whole rationale underlying the understanding and clinical application of this vital topic is clearly and unquestionably inherent simpler, more manageable formula introduced by Henderson (without logs, which is useful and quite adequate for use in medical education.

  11. Structure regulation of silica nanotubes and their adsorption behaviors for heavy metal ions: pH effect, kinetics, isotherms and mechanism.

    Science.gov (United States)

    Wang, Pan; Du, Mingliang; Zhu, Han; Bao, Shiyong; Yang, Tingting; Zou, Meiling

    2015-04-09

    Silica nanotubes (SNTs) with controlled nanotubular structure were synthesized via an electrospinning and calcination process. In this regard, SNTs were found to be ideal adsorbents for Pb(II) removal with a higher adsorption capacity, and surface modification of the SNTs by sym-diphenylcarbazide (SD-SNTs) markedly enhanced the adsorption ability due to the chelating interaction between imino groups and Pb(II). The pH effect, kinetics, isotherms and adsorption mechanism of SNTs and SD-SNTs on Pb(II) adsorption were investigated and discussed detailedly. The adsorption capacity for Pb(II) removal was found to be significantly improved with the decrease of pH value. The Langmuir adsorption model agreed well with the experimental data. As for kinetic study, the adsorption onto SNTs and SD-SNTs could be fitted to pseudo-first-order and pseudo-second-order model, respectively. In addition, the as-prepared SNTs and SD-SNTs also exhibit high adsorption ability for Cd(II) and Co(II). The experimental results demonstrate that the SNTs and SD-SNTs are potential adsorbents and can be used effectively for the treatment of heavy-metal-ions-containing wastewater. Copyright © 2014 Elsevier B.V. All rights reserved.

  12. Double-differential cross section for ionization of H2O molecules by 4-MeV/u C6 + and Si13 + ions

    Science.gov (United States)

    Bhattacharjee, Shamik; Biswas, S.; Monti, J. M.; Rivarola, R. D.; Tribedi, L. C.

    2017-11-01

    Double-differential cross section (DDCS) for electrons ejected in collisions of fast C6 + and Si13 + projectiles, with a H2O vapor target, were measured. The electrons were detected over an energy range of 1-600 eV and an angular range of 20∘-160∘. The obtained DDCS spectra, for both the ions, were compared with the CDW-EIS model. Occasional reference has been made to the DDCS data for the case of 3.75-MeV/u O8 + colliding on the same molecule for an overall comparison. A reasonable agreement with theoretical results was seen for the case of C6 + and O8 + projectiles. However, between C6 + and O8 + projectiles, the deviation from theory is larger for the case of the carbon projectile. Substantial deviation starts to show up for the case of the Si13 + projectile. By numerical integration of the DDCS data, the single-differential cross section (SDCS) and total cross section (TCS) were obtained and compared with theoretical models. The present TCS data along with the other available data for p , He , and C ions were plotted together. A clear and gradual deviation from the Bethe-Born predicted q2 scaling was observed, where q is the projectile charge state. From all the data we find TCS varies as qn where n = 1.7 ± 0.1. The provided data set will be valuable in order to help model the radiation damage in hadron therapy, particularly in the Bragg peak region.

  13. Two different ways that hydrogen ions are involved in the thermodynamics and rapid-equilibrium kinetics of the enzymatic catalysis of S=P and S+H2O=P.

    Science.gov (United States)

    Alberty, Robert A

    2007-07-01

    Hydrogen ions are involved in two different ways in the thermodynamics and rapid-equilibrium kinetics of enzyme-catalyzed reactions. The two ways are through pKs and through the production or consumption of hydrogen ions in the mechanism. These ways are examined for the catalyzed reactions S=P and S+H2O=P. Since the apparent equilibrium constant K' can be calculated from the kinetic parameters by use of the Haldane equation, the treatment of the effects of pH must be consistent in thermodynamics and kinetics. This leads to a new kind of Haldane equation that involves 10(pH) or 10(-pH) in addition to the kinetic parameters when hydrogen ions are produced or consumed. These concepts are applicable to more complicated reactions and rate equations. Derivations of equations for calculating these two types of pH effects are discussed in thermodynamics and rapid-equilibrium kinetics. A computer program is used to make four plots of apparent equilibrium constants and changes in the binding of hydrogen ions in the catalyzed reaction.

  14. Nuclear Magnetic Resonance Structures of GCN4p Are Largely Conserved When Ion Pairs Are Disrupted at Acidic pH but Show a Relaxation of the Coiled Coil Superhelix.

    Science.gov (United States)

    Kaplan, Anne R; Brady, Megan R; Maciejewski, Mark W; Kammerer, Richard A; Alexandrescu, Andrei T

    2017-03-21

    To understand the roles ion pairs play in stabilizing coiled coils, we determined nuclear magnetic resonance structures of GCN4p at three pH values. At pH 6.6, all acidic residues are fully charged; at pH 4.4, they are half-charged, and at pH 1.5, they are protonated and uncharged. The α-helix monomer and coiled coil structures of GCN4p are largely conserved, except for a loosening of the coiled coil quaternary structure with a decrease in pH. Differences going from neutral to acidic pH include (i) an unwinding of the coiled coil superhelix caused by the loss of interchain ion pair contacts, (ii) a small increase in the separation of the monomers in the dimer, (iii) a loosening of the knobs-into-holes packing motifs, and (iv) an increased separation between oppositely charged residues that participate in ion pairs at neutral pH. Chemical shifts (HN, N, C', Cα, and Cβ) of GCN4p display a seven-residue periodicity that is consistent with α-helical structure and is invariant with pH. By contrast, periodicity in hydrogen exchange rates at neutral pH is lost at acidic pH as the exchange mechanism moves into the EX1 regime. On the basis of 1 H- 15 N nuclear Overhauser effect relaxation measurements, the α-helix monomers experience only small increases in picosecond to nanosecond backbone dynamics at acidic pH. By contrast, 13 C rotating frame T 1 relaxation (T 1ρ ) data evince an increase in picosecond to nanosecond side-chain dynamics at lower pH, particularly for residues that stabilize the coiled coil dimerization interface through ion pairs. The results on the structure and dynamics of GCNp4 over a range of pH values help rationalize why a single structure at neutral pH poorly predicts the pH dependence of the unfolding stability of the coiled coil.

  15. 2,4-Dichlorophenoxyacetic acid alters intracellular pH and ion transport in the outer mantle epithelium of the bivalve Anodonta cygnea.

    Science.gov (United States)

    Alves, Marco G; Oliveira, Pedro F

    2014-09-01

    Bivalve molluscs, due to their sedentary mode of life and filter-feeding behavior, are very susceptible to pollutant bioaccumulation and used as sentinel organisms in the assessment of environment pollution. Herein we aimed to determine the in vivo, ex vivo and in vitro effects of 2,4-dichlorophenoxyacetic acid (2,4-D), a widely used herbicide, in Anodonta cygnea shell growth mechanisms. For that, we evaluated the effect of 2,4-D (100 μM) exposure on the transepithelial short-circuit current (Isc), potential (Vt) and conductance (Gt), as well as on OME ion transport systems and intracellular pH (pHi). In vivo exposure to 2,4-D caused an increase of 50% on the Isc generated by OME and ex vivo addition of that compound to the apical side of OME also induced an Isc increase. Furthermore, 2,4-D was able to cause a pHi increase in isolated cells of OME. Noteworthy, when 2,4-D was added following the exposure to specific inhibitors of several membrane transporters identified as responsible for pHi maintenance in these cells, no significant effect was observed on pHi except when the V-type ATPase inhibitor was used, indicating an overlap with the effect of 2,4-D. Thus, we concluded that 2,4-D is able of enhancing the activity of the V-ATPases present on the OME of A. cygnea and that this effect seems to be due to a direct stimulation of those H(+) transporters present on the apical portion of the membrane of OME cells, which are vital for shell maintenance and growth. This study allows us to better understand the molecular mechanisms behind 2,4-D toxicity and its deleterious effect in aquatic ecosystems, with particular emphasis on those involved in shell formation of bivalves. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Effect of thermal oxidation treatment on pH sensitivity of AlGaN/GaN heterostructure ion-sensitive field-effect transistors

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Lei; Bu, Yuyu [Institute of Science and Technology, Tokushima University, Tokushima 770-8506 (Japan); Li, Liuan, E-mail: liliuan@mail.sysu.edu.cn [School of Electronics and Information Technology, Sun Yat-Sen University, Guangzhou 510275 (China); Ao, Jin-Ping, E-mail: jpao@ee.tokushima-u.ac.jp [Institute of Science and Technology, Tokushima University, Tokushima 770-8506 (Japan)

    2017-07-31

    Highlights: • AlGaN/GaN ISFETs were fabricated and evaluated with thermal oxidation treatment. • Sensitivity was improved to 57.7 mV/pH after 700 °C treatment. • Sensitivity became poor after 800 °C treatment. • The pure α-Al{sub 2}O{sub 3} crystal phase generated on the surface of the 700 °C treatment sample. • Ga{sub 2}O{sub 3} phase content in the metal oxide layer increased after 800 °C treatment. - Abstract: In this article, AlGaN/GaN heterostructure ion-sensitive field-effect transistors (ISFETs) were prepared and evaluated by thermal oxidation treatment on the AlGaN surface. The ISFETs were fabricated on the AlGaN/GaN heterostructure and then thermally oxidized with dry oxygen in 600, 700, and 800 °C, respectively. It indicates that the performance of the AlGaN/GaN heterostructure ISFETs, such as noise and sensitivity, has been improved owing to the thermal oxidation treatment process at different temperatures. The X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) results indicate that after thermal oxidation treatment at different temperatures, hydroxide who possesses high surface state density will transfer to oxide owing to the higher chemical stability of the latter. Moreover, a crystalline α-Al{sub 2}O{sub 3} phase generated at 700 °C can not only provide a relatively smooth surface, but also improve the sensitivity to 57.7 mV/pH for the AlGaN/GaN heterostructure ISFETs, which is very close to the Nernstian limit.

  17. A selected ion flow tube study of the ion molecule association reactions of protonated (MH+), nitrosonated (MNO+) and dehydroxidated (M-OH)(+) carboxylic acids (M) with H2O

    Czech Academy of Sciences Publication Activity Database

    Brůhová Michalčíková, R.; Španěl, Patrik

    2014-01-01

    Roč. 368, JUL 2014 (2014), s. 15-22 ISSN 1387-3806 R&D Projects: GA ČR GA13-28882S Institutional support: RVO:61388955 Keywords : ion molecule reactions * proton transfer * selected ion flow tube mass spectrometry Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 1.972, year: 2014

  18. Role of projectile energy and surface work function on charge transfer of negative ions grazing scattering on dissociated H2O-covered Cu(110)

    Science.gov (United States)

    Gao, Lei; Zhu, Yachao; Shi, Yuanqing; Liu, Pinyang; Xiao, Yunqing; Ren, Fei; Chen, Lin; Guo, Yanling; Chen, Ximeng

    2018-01-01

    Shifted Fermi sphere model and parallel velocity effects on clean metals have been verified by a number of previous studies. However, for fast F- and Cl- ions scattering on dissociated water covered Cu(110) at grazing incidence, the negative-ion fraction is projectile dependent and monotonically increases with the increase of impact velocity, which cannot be explained by the conventional parallel velocity effect. The positive-ion fraction increases with the increase of perpendicular velocity, which can be well described by the exponential scaling. Positive ions efficiently formed at large perpendicular velocities strongly suppress the negative ion yield at short distances from the surface, so that negative ions are only formed at large distances. In addition, the large surface work function further promotes a transition between two kinds of parallel velocity effects. The calculation taking into account these contributions is in rough agreement with the experimental data.

  19. F- and H-Area Seepage Basins Water Treatment System Process Optimization and Alternative Chemistry Ion Exchange/Sorbent Material Screening Clearwell Overflow Study

    Energy Technology Data Exchange (ETDEWEB)

    Serkiz, S.M.

    2000-08-30

    This study investigated alternative ion exchange/sorbent materials and polishing chemistries designed to remove specific radionuclides not removed during the neutralization/precipitation/clarification process.

  20. [Dependence of the intracellular concentrations of univalent ions and hydrogenase activity on the salt composition and pH of the medium in the haloalkaliphilic sulfate-reducing bacterium Desulfonatronum thiodismutans].

    Science.gov (United States)

    Soboleva, G S; Dulov, L E; Pusheva, M A

    2007-01-01

    It has been shown that the intracellular concentrations of Na+, K+, and Cl- ions in Desulfonatronum thiodismutans depend on the extracellular concentration of Na' ions. An increase in the extracellular concentration of Na+ results in the accumulation of K+ ions in cells, which points to the possibility that these ions perform an osmoprotective function. When the concentration of the NaCI added to the medium was increased to 4%, the concentration gradient of Cl- ions changed insignificantly. It was found that D. thiodismutans contains two forms of hydrogenase--periplasmic and cytoplasmic. Both enzymes are capable of functioning in solutions with high ionic force; however they exhibit different sensitivities to Na+, K+, and Li+ salts and pH. The enzymes were found to be resistant to high concentrations of Na+ and K+ chlorides and Na+ bicarbonate. The cytoplasmic hydrogenase differed significantly from the periplasmic one in having much higher salt tolerance and lower pH optimum. The activity of these enzymes depended on the nature of both the cationic and anionic components of the salts. For instance, the inhibitory effect of NaCl was less pronounced than that of LiCl, whereas Na+ and Li+ sulfates inhibited the activity of both hydrogenase types to an equal degree. The highest activity of these enzymes was observed at low Na+ concentrations, close to those typical of cells growing at optimal salt concentrations.

  1. Electrical properties of reactive-ion-sputtered Al{sub 2}O{sub 3} on 4H-SiC

    Energy Technology Data Exchange (ETDEWEB)

    Shukla, Madhup, E-mail: madhup.iit@gmail.com [Microelectronics and MEMS Laboratory, Electrical Engineering Department, Indian Institute of Technology Madras, Chennai 600036 (India); Dutta, Gourab [Microelectronics and MEMS Laboratory, Electrical Engineering Department, Indian Institute of Technology Madras, Chennai 600036 (India); Mannam, Ramanjaneyulu [Department of Physics and Nano Functional Materials Technology Centre, Indian Institute of Technology Madras, Chennai 600036 (India); DasGupta, Nandita [Microelectronics and MEMS Laboratory, Electrical Engineering Department, Indian Institute of Technology Madras, Chennai 600036 (India)

    2016-05-31

    Al{sub 2}O{sub 3} was deposited on n-type 4H-SiC by reactive-ion-sputtering (RIS) at room temperature using aluminum target and oxygen as a reactant gas. Post deposition oxygen annealing was carried out at a temperature of 1100 °C. Metal-oxide-semiconductor (MOS) test structures were fabricated on 4H-SiC using RIS-Al{sub 2}O{sub 3} as gate dielectric. The C-V characteristics reveal a significant reduction in flat band voltage for oxygen annealed RIS-Al{sub 2}O{sub 3} samples (V{sub fb} = 1.95 V) compared to as-deposited Al{sub 2}O{sub 3} samples (V{sub fb} > 10 V), suggesting a reduction in negative oxide charge after oxygen annealing. Oxygen annealed RIS-Al{sub 2}O{sub 3} samples also showed significant improvement in I-V characteristics compared to as-deposited RIS-Al{sub 2}O{sub 3} samples. A systematic analysis was carried out to investigate the leakage current mechanisms present in oxygen annealed RIS-Al{sub 2}O{sub 3} on 4H-SiC at higher gate electric field and at different operating temperature. For measurement temperature (T) < 303 K, Fowler–Nordheim (FN) tunneling was found to be the dominant leakage mechanism and for higher temperature (T ≥ 303 K), a combination of FN tunneling and Poole-Frenkel (PF) emission was confirmed. The improvement in I-V characteristics of oxygen annealed RIS-Al{sub 2}O{sub 3}/4H-SiC MOS devices is attributed to large effective barrier height (Φ{sub B} = 2.53 eV) at Al{sub 2}O{sub 3}/SiC interface, due to the formation of an interfacial SiO{sub 2} layer during oxygen annealing, as confirmed from X-ray Photoelectron Spectroscopy results. Further improvement in C-V characteristics for oxygen annealed RIS-Al{sub 2}O{sub 3}/4H-SiC MOS devices was observed after forming gas annealing at 400 °C. - Highlights: • O{sub 2} annealed RIS-Al{sub 2}O{sub 3} on 4H-SiC showed better performance than other reported result. • FN, FN + PF tunneling was found in O{sub 2} annealed RIS-Al{sub 2}O{sub 3} for different temp. ranges. • Al

  2. {sup 1}H and {sup 23}Na MAS NMR spectroscopy of cationic species in CO{sub 2} selective alkaline earth metal porous silicoaluminophosphates prepared via liquid and solid state ion exchange

    Energy Technology Data Exchange (ETDEWEB)

    Arevalo-Hidalgo, Ana G. [Department of Chemical Engineering, University of Puerto Rico-Mayagueez Campus, Mayagueez, PR 00681-9000 (Puerto Rico); Dugar, Sneha; Fu, Riqiang [National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310 (United States); Hernandez-Maldonado, Arturo J., E-mail: arturoj.hernandez@upr.edu [Department of Chemical Engineering, University of Puerto Rico-Mayagueez Campus, Mayagueez, PR 00681-9000 (Puerto Rico)

    2012-07-15

    The location of extraframework cations in Sr{sup 2+} and Ba{sup 2+} ion-exchanged SAPO-34 was estimated by means of {sup 1}H and {sup 23}Na MAS NMR spectroscopy and spectral deconvolution. Incorporation of the alkaline earth metal cations onto the SAPO framework was achieved via liquid state ion exchange, coupled partial detemplation/solid-state ion exchange, and combination of both techniques. MAS NMR revealed that the level of ion exchange was limited by the presence of protons and sodium cations near hexagonal prisms (site SI), which are relatively difficult to exchange with the alkaline earth metal due to steric and charge repulsion criteria. In addition, the presence of ammonium cations in the supercages facilitated the exchange of otherwise tenacious hydrogen as corroborated by unit cell compositional data as well as enhanced CO{sub 2} adsorption at low partial pressures. The extraframework ammonium species were produced from partial detemplation of the structure-directing agent employed for the SAPO-34 synthesis, tetraethylammonium. - Graphical abstract: MAS NMR was used to elucidate the position the cationic species in alkaline earth metal exchanged silicoaluminophosphates. These species played a significant role during the ion exchange process and, therefore, the materials ultimate CO{sub 2} adsorption performance. Highlights: Black-Right-Pointing-Pointer Location of extraframework Sr{sup 2+} or Ba{sup 2+} cations was estimated by means of {sup 1}H and {sup 23}Na MAS NMR. Black-Right-Pointing-Pointer Level of Sr{sup 2+} or Ba{sup 2+} ion exchange was limited by the presence of protons and sodium cations. Black-Right-Pointing-Pointer Presence of ammonium cations in the supercages facilitated the exchange. Black-Right-Pointing-Pointer Sr{sup 2+} and Ba{sup 2+} ion exchanged SAPOs are outstanding CO{sub 2} adsorbents.

  3. Development of a new corona discharge based ion source for high resolution time-of-flight chemical ionization mass spectrometer to measure gaseous H2SO4 and aerosol sulfate

    Science.gov (United States)

    Zheng, Jun; Yang, Dongsen; Ma, Yan; Chen, Mindong; Cheng, Jin; Li, Shizheng; Wang, Ming

    2015-10-01

    A new corona discharge (CD) based ion source was developed for a commercial high-resolution time-of-flight chemical ionization mass spectrometer (HRToF-CIMS) (Aerodyne Research Inc.) to measure both gaseous sulfuric acid (H2SO4) and aerosol sulfate after thermal desorption. Nitrate core ions (NO3-) were used as reagent ions and were generated by a negative discharge in zero air followed by addition of excess nitrogen dioxide (NO2) to convert primary ions and hydroxyl radicals (OH) into NO3- ions and nitric acid (HNO3). The CD-HRToF-CIMS showed no detectable interference from hundreds parts per billion by volume (ppbv) of sulfur dioxide (SO2). Unlike the atmospheric pressure ionization (API) ToF-CIMS, the CD ion source was integrated onto the ion-molecule reaction (IMR) chamber and which made it possible to measure aerosol sulfate by coupling to a filter inlet for gases and aerosols (FIGAERO). Moreover, compared with a quadrupole-based mass spectrometer, the desired HSO4- signal was detected by its exact mass of m/z 96.960, which was well resolved from the potential interferences of HCO3-ṡ(H2O)2 (m/z 97.014) and O-ṡH2OṡHNO3 (m/z 97.002). In this work, using laboratory-generated standards the CD-HRToF-CIMS was demonstrated to be able to detect as low as 3.1 × 105 molecules cm-3 gaseous H2SO4 and 0.5 μg m-3 ammonium sulfate based on 10-s integration time and two times of the baseline noise. The CD ion source had the advantages of low cost and a simple but robust structure. Since the system was non-radioactive and did not require corrosive HNO3 gas, it can be readily field deployed. The CD-HRToF-CIMS can be a powerful tool for both field and laboratory studies of aerosol formation mechanism and the chemical processes that were critical to understand the evolution of aerosols in the atmosphere.

  4. Infrared spectroscopic study of SO42- ions included in M‧2M‧‧(SeO4)2ṡ6H2O (Me‧ = K, NH4+; M‧‧ = Mg, Co, Ni, Cu, Zn) and NH4+ ions included in K2M(XO4)2ṡ6H2O (X = S, Se; M‧‧ = Mg, Co, Ni, Cu, Zn)

    Science.gov (United States)

    Marinova, D.; Karadjova, V.; Stoilova, D.

    2015-01-01

    Infrared spectra of Tutton compounds, M‧2M‧‧(XO4)2ṡ6H2O (M‧ = K, NH4+; M‧‧ = Mg, Co, Ni, Cu, Zn; X = S, Se), as well as those of SO42- guest ions included in selenate host lattices and of NH4+ guest ions included in potassium host lattices are presented and discussed in the regions of ν3 and ν1 of SO42- guest ions, ν4 of NH4+ guest ions and water librations. The SO42- guest ions matrix-isolated in selenate matrices (approximately 2 mol%) exhibit three bands corresponding to ν3 and one band corresponding to ν1 in good agreement with the low site symmetry C1 of the host selenate ions. When the larger SeO42- ions are replaced by the smaller SO42- ions the mean values of the asymmetric stretching modes νbar3 of the included SO42- ions are slightly shifted to lower frequencies as compared to those of the same ions in the neat sulfate compounds due to the smaller repulsion potential of the selenate matrices (larger unit-cell volumes of the selenates). It has been established that the extent of energetic distortion of the sulfate ions matrix-isolated in the ammonium selenates as deduced from the values of Δν3 and Δν3/νc is stronger than that of the same ions matrix-isolated in the potassium selenates due to the formation of hydrogen bonds between the SO42- guest ions with both the water molecules in the host compounds and the NH4+ host ions (for example, Δν3 of the sulfate guest ions have values of 30 and 51 cm-1 in the nickel potassium and ammonium compounds, and 33 and 49 cm-1 in the zinc potassium and ammonium compounds, respectively). The infrared spectra of ammonium doped potassium sulfate matrices show three bands corresponding to Δν4 of the included ammonium ions in agreement with the low site symmetry C1 of the host potassium ions. However, the inclusion of ammonium ions in selenate matrices (with exception of the magnesium compound) leads to the appearance of four bands in the region of ν4. At that stage of our knowledge we assume

  5. High Antifouling Property of Ion-Selective Membrane: toward In Vivo Monitoring of pH Change in Live Brain of Rats with Membrane-Coated Carbon Fiber Electrodes.

    Science.gov (United States)

    Hao, Jie; Xiao, Tongfang; Wu, Fei; Yu, Ping; Mao, Lanqun

    2016-11-15

    In vivo monitoring of pH in live brain remains very essential to understanding acid-base chemistry in various physiological processes. This study demonstrates a potentiometric method for in vivo monitoring of pH in the central nervous system with carbon fiber-based proton-selective electrodes (CF-H + ISEs) with high antifouling property. The CF-H + ISEs are prepared by formation of a H + -selective membrane (H + ISM) with polyvinyl chloride polymeric matrixes containing plasticizer bis(2-ethylhexyl)sebacate, H + ionophore tridodecylamine, and ion exchanger potassium tetrakis(4-chlorophenyl)borate onto carbon fiber electrodes (CFEs). Both in vitro and in vivo studies demonstrate that the H + ISM exhibits strong antifouling property against proteins, which enables the CF-H + ISEs to well maintain the sensitivity and reversibility for pH sensing after in vivo measurements. Moreover, the CF-H + ISEs exhibit a good response to pH changes within a narrow physiological pH range from 6.0 to 8.0 in quick response time with high reversibility and selectivity against species endogenously existing in the central nervous system. The applicability of the CF-H + ISEs is illustrated by real-time monitoring of pH changes during acid-base disturbances, in which the brain acidosis is induced by CO 2 inhalation and brain alkalosis is induced by bicarbonate injections. The results demonstrate that brain pH value rapidly decreases in the amygdaloid nucleus by ca. 0.14 ± 0.01 (n = 5) when the rats breath in pure CO 2 gas, while increases in the cortex by about 0.77 ± 0.12 (n = 3) following intraperitoneal injection of 5 mmol/kg NaHCO 3 . This study demonstrates a new potentiometric method for in vivo measurement of pH change in the live brain of rats with high reliability.

  6. Multi-Isotope Secondary Ion Mass Spectrometry Combining Heavy Water 2H with 15N Labeling As Complementary Tracers for Metabolic Heterogeneity at the Single-Cell Level

    Science.gov (United States)

    Kopf, S.; McGlynn, S.; Cowley, E.; Green, A.; Newman, D. K.; Orphan, V. J.

    2014-12-01

    Metabolic rates of microbial communities constitute a key physiological parameter for understanding the in situ growth constraints for life in any environment. Isotope labeling techniques provide a powerful approach for measuring such biological activity, due to the use of isotopically enriched substrate tracers whose incorporation into biological materials can be detected with high sensitivity by isotope-ratio mass spectrometry. Nano-meter scale secondary ion mass spectrometry (NanoSIMS) combined with stable isotope labeling provides a unique tool for studying the spatiometabolic activity of microbial populations at the single cell level in order to assess both community structure and population diversity. However, assessing the distribution and range of microbial activity in complex environmental systems with slow-growing organisms, diverse carbon and nitrogen sources, or heterotrophic subpopulations poses a tremendous technical challenge because the introduction of isotopically labeled substrates frequently changes the nutrient availability and can inflate or bias measures of activity. Here, we present the use of hydrogen isotope labeling with deuterated water as an important new addition to the isotopic toolkit and apply it for the determination of single cell microbial activities by NanoSIMS imaging. This tool provides a labeling technique that minimally alters any aquatic chemical environment, can be administered with strong labels even in minimal addition (natural background is very low), is an equally universal substrate for all forms of life even in complex, carbon and nitrogen saturated systems, and can be combined with other isotopic tracers. The combination of heavy water labeling with the most commonly used NanoSIMS tracer, 15N, is technically challenging but opens up a powerful new set of multi-tracer experiments for the study of microbial activity in complex communities. We present the first truly simultaneous single cell triple isotope system

  7. Plasma diagnostics of the SIMPA Ecr ion source by X-ray spectroscopy, Collisions of H-like Neon ions with Argon clusters; Diagnostic du plasma de la source d'ions ECR SIMPA par spectroscopie X, Collision d'ions neon hydrogenoides avec des agregats d'argon

    Energy Technology Data Exchange (ETDEWEB)

    Adrouche, N

    2006-09-15

    The first part of this thesis is devoted to the SIMPA ECR ion source characterization, first, I explored the ion source's capacities on the point of view of extracted currents for three elements, argon, krypton and neon. By analyzing the Bremsstrahlung spectra, I determined the electronic temperature in the plasma and the electronic and ionic densities. In a second time, I recorded high resolution X-spectra of argon and krypton plasma's. By taking into account the principal mechanisms of production of a K hole in the ions inside the plasma, I determined the ionic densities of the high charge states of argon. Lastly, I highlighted a correlation between the ions charge states densities with the intensities of extracted currents. The second part of the thesis is devoted to Ne{sup 9+-} argon clusters collisions. First, I presented simple and effective theoretical models allowing to describe the phenomena occurring during a collision, from the point of view of the projectile. I carried out a simulation for a collision of an ion Ne{sup 9+} with an argon cluster of a given size, which has enabled us to know the energy levels populated during the electronic capture and to follow the number of electrons in each projectile shell. Lastly, I presented the first results of a collision between a Ne{sup 9+} beam and argon clusters. These results, have enabled me by using projectile X-ray spectroscopy during the ions-clusters collision, to evidence a strong clustering of targets atoms and to highlight an electronic multi-capture in the projectile ion excited states. (author)

  8. Reactions of hydrated singly charged first-row transition-metal ions M+(H2O)n (M=V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) toward nitric oxide in the gas phase.

    Science.gov (United States)

    van der Linde, Christian; Höckendorf, Robert F; Balaj, O Petru; Beyer, Martin K

    2013-03-11

    Reactions of M(+) (H2 O)n (M=V, Cr, Mn, Fe, Co, Ni, Cu, Zn; n≤40) with NO were studied by Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry. Uptake of NO was observed for M=Cr, Fe, Co, Ni, Zn. The number of NO molecules taken up depends on the metal ion. For iron and zinc, NO uptake is followed by elimination of HNO and formation of the hydrated metal hydroxide, with strong size dependence. For manganese, only small HMnOH(+) (H2 O)n-1 species, which are formed under the influence of room-temperature black-body radiation, react with NO. Here NO uptake competes with HNO formation, both being primary reactions. The results illustrate that, in the presence of water, transition-metal ions are able to undergo quite particular and diverse reactions with NO. HNO is presumably formed through recombination of a proton and (3) NO(-) for M=Fe, Zn, preferentially for n=15-20. For manganese, the hydride in HMnOH(+) (H2 O)n-1 is involved in HNO formation, preferentially for n≤4. The strong size dependence of the HNO formation efficiency illustrates that each molecule counts in the reactions of small ionic water clusters. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Ion Trap Quantum Computing

    Science.gov (United States)

    2011-12-01

    stored ions,” Adv. Atom Mol. Phys., vol. Volume 3, pp. 53–72 1968. [48] P. H. Dawson, Quadrupole Mass Spectometry and Its Applications, Melville, NY... DATE December 2011 3. REPORT TYPE AND DATES COVERED Master’s Thesis 4. TITLE AND SUBTITLE Ion trap Quantum Computing 5. FUNDING NUMBERS 6...researcher [30] that introduced the concept of ion traps in the 1950s. His experiments focused on separating atoms with different masses in order to

  10. Diffusion, Ion Pairing and Aggregation in 1-Ethyl-3-Methylimidazolium-Based Ionic Liquids Studied by 1 H and 19 F PFG NMR: Effect of Temperature, Anion and Glucose Dissolution.

    Science.gov (United States)

    D'Agostino, Carmine; Mantle, Mick D; Mullan, Claire L; Hardacre, Christopher; Gladden, Lynn F

    2018-01-31

    In this work, using 1 H and 19 F PFG NMR, we probe the effect of temperature, ion size/type and glucose dissolution on the rate of transport in 1-ethyl-3-methylimidazolium ([EMIM] + )-based ionic liquids by measuring self-diffusion coefficients. Using such data, we are able to establish the degree of ion pairing and quantify the extent of ionic aggregation during diffusion. For the neat 1-ethyl-3-methylimidazolium acetate ([EMIM][OAc]) a strong degree of ion pairing is observed. The substitution of the [OAc] - anion with the bis{(trifluoromethyl)sulfonyl}imide ([TFSI] - ) anion reduces the pairing between the ions, which is attributed to a lower electric charge density on the [TFSI] - anion, hence a weaker electric interaction with the [EMIM] + cation. The effect of glucose, important for applications of ionic liquids as extracting media, on the strongly paired [EMIM][OAc] sample was also investigated and it is observed that the carbohydrate decreases the degree of ion pairing, which is attributed to the ability of glucose to disrupt inter-ionic interactions by forming hydrogen bonding, particularly with the [OAc] - anion. Calculations of aggregation number from diffusion data show that the [OAc] - anion diffuses as a part of larger aggregates compared to the [EMIM] + cation. The results and analysis presented here show the usefulness of PFG NMR in studies of ionic liquids, giving new insights into ion pairing and aggregation and the factors affecting these parameters. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Negative ion formation and neutralization processes, (1)

    International Nuclear Information System (INIS)

    Sugiura, Toshio

    1982-01-01

    This review has been made preliminary for the purpose of contribute to the plasma heating by ''negative ion based neutral beam injection'' in the magnetic confinement fusion reactor. A compilation includes the survey of the general processes of negative ion formation, the data of the cross section of H - ion formation and the neutralization of H - ion, and some of new processes of H - ion formation. The data of cross section are mainly experimental, but partly include the results of theoretical calculation. (author)

  12. CR-39 track detector calibration for H, He, and C ions from 0.1-0.5 MeV up to 5 MeV for laser-induced nuclear fusion product identification.

    Science.gov (United States)

    Baccou, C; Yahia, V; Depierreux, S; Neuville, C; Goyon, C; Consoli, F; De Angelis, R; Ducret, J E; Boutoux, G; Rafelski, J; Labaune, C

    2015-08-01

    Laser-accelerated ion beams can be used in many applications and, especially, to initiate nuclear reactions out of thermal equilibrium. We have experimentally studied aneutronic fusion reactions induced by protons accelerated by the Target Normal Sheath Acceleration mechanism, colliding with a boron target. Such experiments require a rigorous method to identify the reaction products (alpha particles) collected in detectors among a few other ion species such as protons or carbon ions, for example. CR-39 track detectors are widely used because they are mostly sensitive to ions and their efficiency is near 100%. We present a complete calibration of CR-39 track detector for protons, alpha particles, and carbon ions. We give measurements of their track diameters for energy ranging from hundreds of keV to a few MeV and for etching times between 1 and 8 h. We used these results to identify alpha particles in our experiments on proton-boron fusion reactions initiated by laser-accelerated protons. We show that their number clearly increases when the boron fuel is preformed in a plasma state.

  13. Persistence of gamma-H2AX and 53BP1 foci in proliferating and nonproliferating human mammary epithelial cells after exposure to gamma-rays or iron ions

    Energy Technology Data Exchange (ETDEWEB)

    Groesser, Torsten; Chang, Hang; Fontenay, Gerald; Chen, James; Costes, Sylvain V.; Barcellos-Hoff, Mary Helen; Parvin, Bahram; Rydberg, Bjorn

    2010-12-22

    To investigate {gamma}-H2AX (phosphorylated histone H2AX) and 53BP1 (tumour protein 53 binding protein No. 1) foci formation and removal in proliferating and non-proliferating human mammary epithelial cells (HMEC) after exposure to sparsely and densely ionizing radiation under different cell culture conditions. HMEC cells were grown either as monolayers (2D) or in extracellular matrix to allow the formation of acinar structures in vitro (3D). Foci numbers were quantified by image analysis at various time points after exposure. Our results reveal that in non-proliferating cells under 2D and 3D cell culture conditions, iron-ion induced {gamma}-H2AX foci were still present at 72 h after exposure, although 53BP1 foci returned to control levels at 48 h. In contrast in proliferating HMEC, both {gamma}-H2AX and 53BP1 foci decreased to control levels during the 24-48 h time interval after irradiation under 2D conditions. Foci numbers decreased faster after {gamma}-ray irradiation and returned to control levels by 12 h regardless of marker, cell proliferation status, and cell culture condition. Conclusions: The disappearance of radiation induced {gamma}-H2AX and 53BP1 foci in HMEC have different dynamics that depend on radiation quality and proliferation status. Notably, the general patterns do not depend on the cell culture condition (2D versus 3D). We speculate that the persistent {gamma}-H2AX foci in iron-ion irradiated non-proliferating cells could be due to limited availability of double strand break (DSB) repair pathways in G0/G1-phase, or that repair of complex DSB requires replication or chromatin remodeling.

  14. Ion exchange reactions of major inorganic cations (H+, Na+, Ca2+, Mg2+ and K+) on beidellite: Experimental results and new thermodynamic database. Toward a better prediction of contaminant mobility in natural environments

    International Nuclear Information System (INIS)

    Robin, Valentin; Tertre, Emmanuel; Beaufort, Daniel; Regnault, Olivier; Sardini, Paul; Descostes, Michael

    2015-01-01

    Highlights: • Multi-site ion exchange model for beidellite for Na + , Ca 2+ , Mg 2+ , K + and H + . • Validity over the 1–7 pH range and total normality >5 × 10 −3 mol/L. • Application to equilibrium between smectite and acidic solution from mining sites. • Impact of crystal chemistry of smectites on their sorption properties. - Abstract: To our knowledge, no thermodynamic database is available in the literature concerning ion-exchange reactions occurring in low-charge smectite with tetrahedral charge (beidellite). The lack of this information makes it difficult to predict the mobility of contaminants in environments where beidellite and major cations, which act as competitors with contaminants for sorption on the clay phase, are present. The present study proposes a multi-site ion exchange model able to describe experimental data obtained for H + and the four major cations (Na + , Ca 2+ , Mg 2+ and K + ) found in natural waters interacting with a <0.3 μm size fraction of Na-beidellite. The nature of the sites involved in the sorption processes is assessed using qualitative structural data. Moreover, the effect of the charge location in the smectite on the selectivity coefficient values is discussed by comparison with the results reported in the literature for smectite characterized by octahedral charge (montmorillonite). The new thermodynamic database proposed in this study is based on the same total sorption site density and distribution of sites regardless of the cations investigated. This database is valid for a large range of physico-chemical conditions: a [1–7] pH range, a total normality higher than 5 × 10 −3 mol/L corresponding to a flocculated state for water/clay systems, and when sorption of ions pairs can be neglected. Note that this study provides evidence that a thermodynamic database describing ion exchange reactions between H + and the four major cations of natural water for smectite cannot be valid irrespective of the total

  15. Radiative electron capture by bare and H-like Si and Cl ions using the channeling technique and the associated solid-state effect

    Energy Technology Data Exchange (ETDEWEB)

    Tribedi, L.C.; Nanal, V.; Kurup, M.B.; Prasad, K.G.; Tandon, P.N. (Tata Institute of Fundamental Research, Bombay 400 005 (India))

    1995-02-01

    Fully stripped and hydrogenlike Si and Cl ions, in the energy range 2--5 MeV/amu and channeled through a 0.17 [mu]m thick Si single crystal, were used to study the radiative electron capture (REC) into the [ital K] shell of the ions. The associated effects due to the solid medium of the target were also investigated from the energy and the derived cross section of the REC photons. The [ital K]-shell REC cross sections were found to fall on a universal curve when plotted against the adiabaticity parameter of the collision system. The measured energy shifts in the REC photon energy and the higher yield of REC photons using crystalline targets, as compared to the available gas-target data, are indicative of an ion--solid-state effect'' caused by the electron-wake potential. The magnitude of these effects is shown to increase with [ital Z]/[ital v] of an ion with charge [ital Z] and velocity [ital v], and are in qualitative agreement with recent calculations. The REC cross sections are, however, observed to be slightly smaller than the theoretical estimates after taking into account the effects associated with the solid medium. The widths of the REC peaks are compared with the theoretical models. The results of the present investigation using Si and Cl ions are presented coherently along with our earlier data using lighter ions.

  16. Mechanical properties of 6H-SiC irradiated by neutron and MeV heavy ions: A nanoindentation and finite element method study

    Science.gov (United States)

    Chen, Xiaofei; Zhou, Wei; Zhang, Xuxin; Feng, Qijie; Zheng, Jian; Liu, Xiankun; Tang, Bin; Li, Jiangbo; Xue, Jianming; Peng, Shuming

    2018-01-01

    Understanding the mechanical properties of structural materials under an irradiation environment stands as a major challenge for developing advanced nuclear systems. In this paper, the mechanical properties, including the Young's modulus, yield stress, and hardness, of SiC samples irradiated by neutron and heavy ions (3 MeV C and Si ions) have been investigated by nanoindentation measurement. When the load-depth curves were analyzed by the widely used Oliver-Pharr method, for the samples irradiated at the same displacement damage level (0.1 and 0.2 dpa), both the elastic modulus and hardness of the ion irradiated SiC are significantly higher compared with those of neutron irradiated samples. The discrepancy is mainly attributed to the irradiation induced surface lateral stress in ion irradiated samples, which cannot be taken into account for the Oliver-Pharr method. After carefully considering this effect by the finite element method in simulating the load-depth curves, both the Young's modulus and yield stress of ion irradiated samples agree well with those of neutron irradiated samples. This study reveals that by the combined method of nanoindentation and finite element, the mechanical properties, including the Young's modulus, yield stress and hardness, for neutron irradiated SiC can be reasonably evaluated by MeV heavy ion irradiation.

  17. Ion source

    International Nuclear Information System (INIS)

    Saito, Fusao; Okuyama, Toshihisa; Suzuki, Yasuo.

    1996-01-01

    In a negative ion source having magnetic filters, bisecting magnetic fields are formed using electromagnets disposed at the outside of a plasma source. The position of the electromagnets is made adjustable and removable to optimize a negative ion generation efficiency. Further, a plurality of electromagnets are disposed in longitudinal direction of the plasma source, and the intensity of the magnetic fields of the filters in the longitudinal direction is made adjustable to control a beam distribution. Since uniform magnetic fields which bisect the plasma source can be formed by the electromagnets, and magnetomotive force of the electromagnets can be increased easily compared with that of permanent magnets, the magnetomotive force is changed to obtain appropriate filter magnetic fields easily. Then, optimum magnetic fields corresponding to the state of source plasmas can be generated by the control of the power source of the electromagnets, which also increases the negative ion drawing current density, thereby enabling to reduce the drawing area and size of the plasma source. (N.H.)

  18. High Lithium Insertion Voltage Single-Crystal H2 Ti12 O25 Nanorods as a High-Capacity and High-Rate Lithium-Ion Battery Anode Material.

    Science.gov (United States)

    Guo, Qiang; Chen, Li; Shan, Zizhao; Lee, Wee Siang Vincent; Xiao, Wen; Liu, Zhifang; Liang, Jingjing; Yang, Gaoli; Xue, Junmin

    2018-01-10

    H 2 Ti 12 O 25 holds great promise as a high-voltage anode material for advanced lithium-ion battery applications. To enhance its electrochemical performance, control of the crystal orientation and morphology is an effective way to cope with slow Li + -ion diffusion inside H 2 Ti 12 O 25 with severe anisotropy. In this report, Na 2 Ti 6 O 13 nanorods, prepared from Na 2 CO 3 and anatase TiO 2 in molten NaCl medium, were used as a precursor in the synthesis of long single-crystal H 2 Ti 12 O 25 nanorods with reactive facets. The as-prepared H 2 Ti 12 O 25 nanorods with a diameter of 100-200 nm showed higher charge (extraction) specific capacity and better rate performance than previously reported systems. The reversible capacity of H 2 Ti 12 O 25 was 219.8 mAh g -1 at 1C after 100 cycles, 172.1 mAh g -1 at 10C, and 144.4 mAh g -1 at 20C after 200 cycles; these values are higher than those of H 2 Ti 12 O 25 prepared by the conventional soft-chemical method. Moreover, the as-prepared H 2 Ti 12 O 25 nanorods exhibited superior cycle stability with more than 94 % retention of capacity with nearly 100 % coulombic efficiency after 100 cycles at 1C. On the basis of the above results, long single-crystal H 2 Ti 12 O 25 nanorods synthesized in molten NaCl with outstanding electrochemical characteristics hold a significant amount of promise for hybrid electric vehicles and energy-storage systems. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Accurate stopping power measurements for (0.21–2.68) MeV/u {sup 1}H{sup +} and {sup 4}He{sup +} ions crossing thin Al foils; extraction of the (I, b) parameters

    Energy Technology Data Exchange (ETDEWEB)

    Moussa, D., E-mail: djamelmoussa@gmail.com [Université des Sciences et Technologie H. Boumediene (USTHB), Laboratoire SNIRM, Faculté de Physique, B.P. 32, 16111 Bab-Ezzouar, Algiers (Algeria); Damache, S. [Division de Physique, CRNA, 02 Bd. Frantz Fanon, B.P. 399 Alger-gare, Algiers (Algeria); Ouichaoui, S., E-mail: souichaoui@gmail.com [Université des Sciences et Technologie H. Boumediene (USTHB), Laboratoire SNIRM, Faculté de Physique, B.P. 32, 16111 Bab-Ezzouar, Algiers (Algeria)

    2015-01-15

    The stopping powers of thin Al foils for H{sup +} and {sup 4}He{sup +} ions have been measured over the energy range E=(206.03–2680.05) keV/amu with an overall relative uncertainty better than 1% using the transmission method. The derived S(E) experimental data are compared to previous ones from the literature, to values derived by the SRIM-2008 code or compiled in the ICRU-49 report, and to the predictions of Sigmund–Schinner binary collision stopping theory. Besides, the S(E) data for H{sup +} ions together with those for He{sup 2+} ions reported by Andersen et al. (1977) have been analyzed over the energy interval E>1.0 MeV using the modified Bethe–Bloch stopping theory. The following sets of values have been inferred for the mean excitation potential, I, and the Barkas–Andersen parameter, b, for H{sup +} and He{sup +} projectiles, respectively: {(I=164±3)) eV, (b=1.40} and {(I=163±2.5)) eV, (b=1.38}. As expected, the I parameter is found to be independent of the projectile electronic structure presumably indicating that the contribution of charge exchange effects becomes negligible as the projectile velocity increases. Therefore, the I parameter must be determined from precise stopping power measurements performed at high projectile energies where the Bethe stopping theory is fully valid.

  20. Electronic stopping power of slow H{sup +} and He{sup 2+} ions in CdTe from first principle

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chang-kai [The Key Laboratory of Beam Technology and Material Modification of Ministry of Education, College of Nuclear Science and Technology, Beijing Normal University, Beijing 100875 (China); Beijing Radiation Center, Beijing 100875 (China); Mao, Fei [School of Nuclear Science and Technology, University of South China, Hengyang 421001 (China); Fu, Yan-long; Liao, Bin [The Key Laboratory of Beam Technology and Material Modification of Ministry of Education, College of Nuclear Science and Technology, Beijing Normal University, Beijing 100875 (China); Beijing Radiation Center, Beijing 100875 (China); Ouyang, Xiao-ping [Northwest Institute of Nuclear Technology, Xi’an 710024 (China); Zhang, Feng-Shou, E-mail: fszhang@bnu.edu.cn [The Key Laboratory of Beam Technology and Material Modification of Ministry of Education, College of Nuclear Science and Technology, Beijing Normal University, Beijing 100875 (China); Beijing Radiation Center, Beijing 100875 (China); Center of Theoretical Nuclear Physics, National Laboratory of Heavy Ion Accelerator of Lanzhou, Lanzhou 730000 (China)

    2017-02-01

    We study through time-dependent density-functional theory (TDDFT) method the electronic stopping power of low-energy protons and helium ions moving through CdTe under the condition of channeling. The agreement between our calculated results and SRIM data roughly up to the stopping maximum for the proton along the 〈1 0 0〉 and 〈1 1 1〉 crystalline axes and for helium ions along 〈1 0 0〉 crystalline axis is satisfactory, which can be explained by the energy transfer mechanism that electron–hole excitation caused by ions in the solid. However, in the channel of 〈1 1 1〉 for helium ions, a transition between two velocities regimes is observed at about v = 0.4 a.u. This may be an indication of extra energy loss channel beyond the electron–hole excitation. To analyze it, we calculate the amount of electrons captured by the moving projectiles in real time. It is found that the soft transition between two velocities regimes can be attributed to the charge transfer and charge resonance between helium ion and host atoms of CdTe crystal, which are considered as additional energy loss channels.

  1. Column solid phase extraction and flame atomic absorption spectrometric determination of manganese(II) and iron(III) ions in water, food and biological samples using 3-(1-methyl-1H-pyrrol-2-yl)-1H-pyrazole-5-carboxylic acid on synthesized graphene oxide.

    Science.gov (United States)

    Pourjavid, Mohammad Reza; Sehat, Ali Akbari; Arabieh, Masoud; Yousefi, Seyed Reza; Hosseini, Majid Haji; Rezaee, Mohammad

    2014-02-01

    A modified, selective, highly sensitive and accurate procedure for the determination of trace amounts of manganese and iron ions is established in the presented work. 3-(1-Methyl-1H-pyrrol-2-yl)-1H-pyrazole-5-carboxylic acid (MPPC) and graphene oxide (GO) were used in a glass column as chelating reagent and as adsorbent respectively prior to their determination by flame atomic absorption spectrometry. The adsorption mechanism of titled metals complexes on GO was investigated by using computational chemistry approach based on PM6 semi-empirical potential energy surface (PES). The effect of some parameters including pH, flow rate and volume of sample and type, volume and concentration of eluent, as well as the adsorption capacity of matrix ions on the recovery of Mn(II) and Fe(III) was investigated. The limit of detection was 145 and 162 ng L(-1) for Mn(II) and Fe(III), respectively. Calibration was linear over the range of 0.31-355 μg L(-1) for Mn(II) and 0.34-380 μg L(-1) for Fe(III) ions. The method was successfully applied for the determination of understudied ions in water, food and biological samples. Copyright © 2013 Elsevier B.V. All rights reserved.

  2. Molecular ion sources for low energy semiconductor ion implantation (invited).

    Science.gov (United States)

    Hershcovitch, A; Gushenets, V I; Seleznev, D N; Bugaev, A S; Dugin, S; Oks, E M; Kulevoy, T V; Alexeyenko, O; Kozlov, A; Kropachev, G N; Kuibeda, R P; Minaev, S; Vizir, A; Yushkov, G Yu

    2016-02-01

    Smaller semiconductors require shallow, low energy ion implantation, resulting space charge effects, which reduced beam currents and production rates. To increase production rates, molecular ions are used. Boron and phosphorous (or arsenic) implantation is needed for P-type and N-type semiconductors, respectively. Carborane, which is the most stable molecular boron ion leaves unacceptable carbon residue on extraction grids. A self-cleaning carborane acid compound (C4H12B10O4) was synthesized and utilized in the ITEP Bernas ion source resulting in large carborane ion output, without carbon residue. Pure gaseous processes are desired to enable rapid switch among ion species. Molecular phosphorous was generated by introducing phosphine in dissociators via 4PH3 = P4 + 6H2; generated molecular phosphorous in a pure gaseous process was then injected into the HCEI Calutron-Bernas ion source, from which P4(+) ion beams were extracted. Results from devices and some additional concepts are described.

  3. Collisions of slow polyatomic ions with surfaces: Dissociation and chemical reactions of C2H2+ center dot, C2H3+, C2H4+ center dot C2H5+, and their deuterated variants C2D2+ center dot and C2D4+ center dot on room-temperature and heated carbon surfaces

    Czech Academy of Sciences Publication Activity Database

    Jašík, J.; Žabka, Ján; Feketeová, L.; Ipolyi, I.; Märk, T. D.; Herman, Zdeněk

    2005-01-01

    Roč. 109, č. 45 (2005), s. 10208-10215 ISSN 1089-5639 R&D Projects: GA AV ČR IAA4040405; GA AV ČR KSK4040110; GA MŠk LC510 Institutional research plan: CEZ:AV0Z40400503 Keywords : ethanol molecular-ions * hydrocarbon films * internal energy * projectile ions Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.898, year: 2005

  4. Evaluation of differences between dual salt-pH gradient elution and mono gradient elution using a thermodynamic model: Simultaneous separation of six monoclonal antibody charge and size variants on preparative-scale ion exchange chromatographic resin.

    Science.gov (United States)

    Lee, Yi Feng; Jöhnck, Matthias; Frech, Christian

    2018-02-21

    The efficiencies of mono gradient elution and dual salt-pH gradient elution for separation of six mAb charge and size variants on a preparative-scale ion exchange chromatographic resin are compared in this study. Results showed that opposite dual salt-pH gradient elution with increasing pH gradient and simultaneously decreasing salt gradient is best suited for the separation of these mAb charge and size variants on Eshmuno ® CPX. Besides giving high binding capacity, this type of opposite dual salt-pH gradient also provides better resolved mAb variant peaks and lower conductivity in the elution pools compared to single pH or salt gradients. To have a mechanistic understanding of the differences in mAb variants retention behaviors of mono pH gradient, parallel dual salt-pH gradient, and opposite dual salt-pH gradient, a linear gradient elution model was used. After determining the model parameters using the linear gradient elution model, 2D plots were used to show the pH and salt dependencies of the reciprocals of distribution coefficient, equilibrium constant, and effective ionic capacity of the mAb variants in these gradient elution systems. Comparison of the 2D plots indicated that the advantage of opposite dual salt-pH gradient system with increasing pH gradient and simultaneously decreasing salt gradient is the noncontinuous increased acceleration of protein migration. Furthermore, the fitted model parameters can be used for the prediction and optimization of mAb variants separation in dual salt-pH gradient and step elution. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 2018. © 2018 American Institute of Chemical Engineers.

  5. Fluorine negative ion detachment kinetics

    Science.gov (United States)

    Burke, R. R.; Miller, W. J.; Gould, R. K.

    1971-01-01

    A study of the rate of F(-) detachment by O and H atoms via the reactions F(-) + O yields FO + e and F(-) + H yields FH+ e was undertaken using a drift tube to produce F(-) ions at various drift velocities and therefore different ion temperatures. Preliminary mobility measurements of F(-) ions in Ar were made, indicating that ion temperatures in the 300 K to 5000 K range could be achieved; however due to numerous difficulties experienced in obtaining a reliable F(-) ion source, the study could not be completed.

  6. Raman and DFT Study on N-H+…Cl- Hydrogen Bonding in 1,1,3,3-Tetra-Methylguanidinium Chloride forming an Ion-pair Molecule in the Vapor Phase

    DEFF Research Database (Denmark)

    Berg, Rolf W.; Riisager, Anders; Fehrmann, Rasmus

    The chemistry of 1,1,3,3-tetramethylguanidinium ([TMGH]+) chloride, a low temperature (molten) ionic liquid, is discussed, based on its Raman spectra associated with ab initio molecular orbital DFT-type quantum mechanical calculations (with 6-311+G(d,p) basis sets) on “molecules” in isolated...... gaseous free states without any assumed symmetry. The calculations on the monomeric [TMGH]+ ion and the dimeric ion pair converged to give geometries near the established crystal structure of the [TMGH]Cl salt. This salt is known to contain dimeric ion pairs of the kind [TMGH]ClCl[TMGH](Fig.1...... that dimeric molecular ion pairs with four N-H+…Cl- hydrogen bonds seem to exist also in the solutions, and probably are responsible for the relatively high solubility of the “salt” in ethanol. The “salt” can be easily sublimed at about 200-230 oC. The Raman spectrum of the vapor at 225 ºC has a characteristic...

  7. Ohmic contact on n- and p-type ion-implanted 4H-SiC with low-temperature metallization process for SiC MOSFETs

    Science.gov (United States)

    Shimizu, Haruka; Shima, Akio; Shimamoto, Yasuhiro; Iwamuro, Noriyuki

    2017-04-01

    The ohmic contact on n- and p-type SiC regions with the same contact metal is a key process in regard to creating high-performance MOSFETs and insulated gate bipolar transistors (IGBTs). The dependence of the contact resistance on n- and p-type SiC regions on ion species, dose, and implantation temperature was investigated. The results of such an investigation revealed that the amorphization of the SiC surface and the generation of 3C-SiC produce a low contact resistance without the need for a high-temperature metallization process. The contact resistances of 2.1 × 10-6 Ω cm2 on the n-type SiC region and 1.3 × 10-3 Ω cm2 on the p-type SiC region were obtained with high-dose ion implantation at room temperature on the n-type SiC region, high-dose ion implantation at high temperature on the p-type SiC region, and a titanium-based contact electrode. A SiC MOSFET was fabricated with the low-temperature ohmic contact process. The positive-bias gate leakage current markedly increased. It can be deduced that high-dose ion implantation at room temperature on the n-type SiC region degrades surface roughness on the N+ source region.

  8. Alkylsulfonates as probes of uncoupling protein transport mechanism. Ion pair transport demonstrates that direct H(+) translocation by UCP1 is not necessary for uncoupling

    Czech Academy of Sciences Publication Activity Database

    Jabůrek, M.; Vařecha, M.; Ježek, Petr; Garlid, K. D.

    2001-01-01

    Roč. 276, č. 34 (2001), s. 31897-31905 ISSN 0021-9258 R&D Projects: GA AV ČR IAA5011106 Grant - others:NIH(US) DK56273 Institutional research plan: CEZ:AV0Z5011922 Keywords : mitochondrial uncoupling proteins * alkylsulfonates * ion pair transport Subject RIV: CE - Biochemistry Impact factor: 7.258, year: 2001

  9. Electrolysis of H2O and CO2 in an oxygen-ion conducting solid oxide electrolyzer with a La0.2Sr0.8TiO3+δ composite cathode

    Science.gov (United States)

    Li, Shisong; Li, Yuanxin; Gan, Yun; Xie, Kui; Meng, Guangyao

    2012-11-01

    Solid oxide electrolyzers have attracted a great deal of interest in recent years because they can convert electrical energy into chemical energy with high efficiency. Ni/YSZ cathodes are generally utilized for high temperature electrolysis of H2O and CO2 in oxygen-ion conducting solid oxide electrolyzers; however, such electrodes can only operate under reducing conditions. In an atmosphere without a flow of reducing gas, cathodes based on La0.2Sr0.8TiO3+δ (LST) are a promising alternative. Solid Oxide Electrolyzers with LST cathodes without pre-reduction were used at 700 °C for the electrolysis of 3%H2O/97%N2 and 100%CO2, and promising polarization impedance data were obtained in both atmospheres. The electrochemical results indicated that the electrochemical reduction of the La0.2Sr0.8TiO3+δ cathode was the main process at low electrical voltages, while the electrolysis was the main process at high voltages because ion transportation in the electrolyte limited the overall efficiency. The electrolysis of H2O was determined to be more efficient than the electrolysis of CO2 under the same conditions. The Faraday efficiencies of H2O and CO2 were 85.0% and 24.7%, respectively, at 700 °C and a 2 V applied potential.

  10. Evaluation of pH and calcium ion release of a dual-cure bisphenol A ethoxylate dimethacrylate/mineral trioxide aggregate-based root-end filling material.

    Science.gov (United States)

    Linhares, Giane da Silva; Cenci, Maximiliano Sérgio; Knabach, César Blaas; Oliz, Camila Mizette; Vieira, Mariana Antunes; Ribeiro, Anderson Schwingel; Zanchi, César Henrique; Jacinto, Rogério Castilho

    2013-12-01

    The incorporation of light-curable resins has been proposed for mineral trioxide aggregate (MTA) to improve its properties and reduce its setting time. The aim of the present study was to assess the pH and calcium ion release of an experimental bisphenol A ethoxylate dimethacrylate/MTA-based root-end filling material (E-MTA) in comparison with white MTA Angelus (Angelus, Londrina, PR, Brazil) (W-MTA) and to evaluate the influence of the addition of calcium chloride (CaCl2) on these properties. Polyethylene tubes filled with the materials were immersed in deionized water for the measurement of pH (digital pH meter) and calcium release (atomic absorption spectrophotometry). The evaluations were performed at 3 and 24 hours and 7, 15, and 30 days. Data were measured using 2-way repeated measures of variance followed by the Holm-Sidak method (P MTA showed a significantly lower calcium ion release capacity when compared with W-MTA (P MTA + 5% CaCl2 was similar to W-MTA (P > .05). The monomer bisphenol A ethoxylate dimethacrylate added to MTA formed a material with a lower capacity of calcium release than W-MTA despite maintaining a similar pH. However, the addition of CaCl2 improved the calcium release of this material. Copyright © 2013 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  11. Evidence for Sequence Scrambling and Divergent H/D Exchange Reactions of Doubly-Charged Isobaric b-Type Fragment Ions

    Science.gov (United States)

    Zekavat, Behrooz; Miladi, Mahsan; Al-Fdeilat, Abdullah H.; Somogyi, Arpad; Solouki, Touradj

    2014-02-01

    To date, only a limited number of reports are available on structural variants of multiply-charged b-fragment ions. We report on observed bimodal gas-phase hydrogen/deuterium exchange (HDX) reaction kinetics and patterns for substance P b10 2+ that point to presence of isomeric structures. We also compare HDX reactions, post-ion mobility/collision-induced dissociation (post-IM/CID), and sustained off-resonance irradiation-collision induced dissociation (SORI-CID) of substance P b10 2+ and a cyclic peptide with an identical amino acid (AA) sequence order to substance P b10. The observed HDX patterns and reaction kinetics and SORI-CID pattern for the doubly charged head-to-tail cyclized peptide were different from either of the presumed isomers of substance P b10 2+, suggesting that b10 2+ may not exist exclusively as a head-to-tail cyclized structure. Ultra-high mass measurement accuracy was used to assign identities of the observed SORI-CID fragment ions of substance P b10 2+; over 30 % of the observed SORI-CID fragment ions from substance P b10 2+ had rearranged (scrambled) AA sequences. Moreover, post-IM/CID experiments revealed the presence of two conformer types for substance P b10 2+, whereas only one conformer type was observed for the head-to-tail cyclized peptide. We also show that AA sequence scrambling from CID of doubly-charged b-fragment ions is not unique to substance P b10 2+.

  12. Tandem Mass Spectrometry and Ion Mobility Reveals Structural Insight into Eicosanoid Product Ion Formation.

    Science.gov (United States)

    Di Giovanni, James P; Barkley, Robert M; Jones, David N M; Hankin, Joseph A; Murphy, Robert C

    2018-04-23

    Ion mobility measurements of product ions were used to characterize the collisional cross section (CCS) of various complex lipid [M-H] - ions using traveling wave ion mobility mass spectrometry (TWIMS). TWIMS analysis of various product ions derived after collisional activation of mono- and dihydroxy arachidonate metabolites was found to be more complex than the analysis of intact molecular ions and provided some insight into molecular mechanisms involved in product ion formation. The CCS observed for the molecular ion [M-H] - and certain product ions were consistent with a folded ion structure, the latter predicted by the proposed mechanisms of product ion formation. Unexpectedly, product ions from [M-H-H 2 O-CO 2 ] - and [M-H-H 2 O] - displayed complex ion mobility profiles suggesting multiple mechanisms of ion formation. The [M-H-H 2 O] - ion from LTB 4 was studied in more detail using both nitrogen and helium as the drift gas in the ion mobility cell. One population of [M-H-H 2 O] - product ions from LTB 4 was consistent with formation of covalent ring structures, while the ions displaying a higher CCS were consistent with a more open-chain structure. Using molecular dynamics and theoretical CCS calculations, energy minimized structures of those product ions with the open-chain structures were found to have a higher CCS than a folded molecular ion structure. The measurement of product ion mobility can be an additional and unique signature of eicosanoids measured by LC-MS/MS techniques. Graphical Abstract ᅟ.

  13. Metal-organic frameworks with 1,4-di(1H-imidazol-4-yl)benzene and varied carboxylate ligands for selectively sensing Fe(iii) ions and ketone molecules.

    Science.gov (United States)

    Liu, Zhi-Qiang; Zhao, Yue; Zhang, Xiu-Du; Kang, Yan-Shang; Lu, Qing-Yi; Azam, Mohammad; Al-Resayes, Saud I; Sun, Wei-Yin

    2017-10-17

    Four new metal-organic frameworks (MOFs) [Zn(L)(bpdc)]·1.6H 2 O (1), [Co(L)(bpdc)]·H 2 O (2), [Ni 3 (L) 2 (bptc) 2 (H 2 O) 10 ]·2H 2 O (3) and [Cd 2 (L)(Hbptc) 2 ] (4) were achieved by reactions of the corresponding metal salt with mixed organic ligands of 1,4-di(1H-imidazol-4-yl)benzene (L) and 4,4'-benzophenonedicarboxylic acid (H 2 bpdc) or biphenyl-2,4',5-tricarboxylic acid (H 3 bptc). They exhibit varied structures: MOFs 1 and 4 are porous three-dimensional (3D) frameworks, while 2 is an infinite one-dimensional (1D) chain and 3 is a two-dimensional (2D) network. Remarkably, 1 and 4 can act as potential fluorescent materials for sensing Fe(iii) ions and different ketone molecules with high selectivity and sensitivity. In addition, MOF 1 shows selective adsorption of CO 2 over N 2 .

  14. Studies on phase and morphological evolution of silver vanadium oxides as a function of pH: evaluation of electrochemical behavior towards quantification of Pb2+ and Cd2+ ions

    Science.gov (United States)

    Gangaiah, Vijayakumar; Shivappa Adarakatti, Prashanth; Siddaramanna, Ashoka; Malingappa, Pandurangappa; Thimmanna Chandrappa, Gujjarahalli

    2017-08-01

    The effect of pH on morphological and phase evolution of silver vanadium oxide nanostructures are investigated under hydrothermal process. The results of powder x-ray diffraction (PXRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) disclosed that the morphological evolution of nanobelts into nanoring structures occurs at pH in between 4 and 5 with Ag2V4O11 phase and nanobelt morphologies at pH from 6 to 7 with β-AgVO3 phase. The prepared Ag2V4O11 and β-AgVO3 have been evaluated for the simultaneous quantification of Pb2+ and Cd2+ ions in aqueous solution using differential pulse anodic stripping voltammetry. The results reveal that Ag2V4O11 shows better quantification result compared to β-AgVO3.

  15. Ion implantation in ices

    International Nuclear Information System (INIS)

    Strazzulla, G.; Baratta, G.A.; Palumbo, M.E.; Satorre, M.A.

    2000-01-01

    We have studied, by in situ infrared spectroscopy, some effects due to ion implantation in frozen ices. In particular mixtures containing C, N and O atoms (e.g., N 2 :H 2 O:CH 4 ) have been irradiated with unreactive (noble gases) ions: the resulting alteration of the frozen sample induces the formation of other molecules (e.g., CO 2 , R- - -OCN, CO and HCN) and of a refractory organic residue. Similar products are formed when mixtures containing only C and O atoms (e.g., H 2 O:CH 4 ) are irradiated with N ions, i.e. molecular species that include the projectile are formed. These results are important, in particular for their applications to planetary physics. In planetary environments ice thickness is usually much larger than the penetration depth of the relevant ion populations (solar wind ions, magnetospheric particles, etc.) and ion implantation phenomena are expected. Our results indicate that some molecular species observed on icy planetary surfaces could not be native of that object but formed by ion irradiation and/or by implantation of reactive ions

  16. Inhibition of mild steel corrosion by 1,4,6-trimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile and synergistic effect of halide ion in 0.5 M H{sub 2}SO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Mourya, Punita, E-mail: mouryapunita025@gmail.com [Department of Chemistry, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005 (India); Singh, Praveen [Department of Chemistry, Banaras Hindu University, Varanasi 221005 (India); Rastogi, R.B.; Singh, M.M. [Department of Chemistry, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005 (India)

    2016-09-01

    Highlights: • TODPCN is a good corrosion inhibitor for mild steel in 0.5 M H{sub 2}SO{sub 4} solution. • Addition of iodide ion increases the inhibition efficiency of the studied nitrile derivative. • Inhibition efficiency successively increases with concentration. • XPS study has revealed the chemical composition of the protective film. - Abstract: The effect of iodide ions on inhibitive performance of 1,4,6-trimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile (TODPCN) on mild steel (MS) corrosion in 0.5 M H{sub 2}SO{sub 4} was studied using gravimetric and electrochemical measurements. TODPCN inhibits the corrosion of MS to the extent of 62.3% at its lowest concentration (0.5 mM) and its inhibition efficiency (η) further increases on increasing concentration at 298 K. The adsorption of TODPCN on MS was found to follow the Langmuir adsorption isotherm. The value of η increased on the addition of 2.0 mM KI. The value of synergism parameter being more than unity indicates that the enhanced η value in the presence of iodide ions is only due to synergism. Thus, a cooperative mechanism of inhibition exists between the iodide anion and TODPCN cations. The increase in surface coverage in the presence of KI indicates that iodide ions enhance the adsorption of TODPCN. The surface morphology of corroded/inhibited MS was studied by atomic force microscopy. X-ray photoelectron spectroscopy of inhibited MS surface was carried out to determine the composition of the adsorbed film. Some quantum chemical parameters and the Mulliken charge densities for TODPCN calculated by density functional theory provided further insight into the mechanism of inhibition.

  17. A plant wide aqueous phase chemistry model describing pH variations and ion speciation/pairing in wastewater treatment process models

    DEFF Research Database (Denmark)

    Flores-Alsina, X.; Mbamba, C. Kazadi; Solon, K.

    /pairing is presented and interfaced with industry standard models. The module involves extensive consideration of non-ideality by including ion activities instead of molar concentrations and complex ion pairing. The general equilibria are formulated as a set of Differential Algebraic Equations (DAEs) instead......There is a growing interest within the Wastewater Treatment Plant (WWTP) modelling community to correctly describe physico-chemical processes after many years of mainly focusing on biokinetics (Batstone et al., 2012). Indeed, future modelling needs, such as a plant-wide phosphorus (P) description...... cationic/anionic loads. In this way, the general applicability/flexibility of the proposed approach is demonstrated by implementing the aqueous phase chemistry module in some of the most frequently used WWTP process simulation models. Finally, it is shown how traditional wastewater modelling studies can...

  18. A plant-wide aqueous phase chemistry module describing pH variations and ion speciation/pairing in wastewater treatment process models

    DEFF Research Database (Denmark)

    Flores Alsina, Xavier; Kazadi Mbamba, Christian; Solon, Kimberly

    2015-01-01

    standard models. The module accounts for extensive consideration of non-ideality, including ion activities instead of molar concentrations and complex ion pairing. The general equilibria are formulated as a set of Differential Algebraic Equations (DAEs) instead of Ordinary Differential Equations (ODEs......There is a growing interest within the Wastewater Treatment Plant (WWTP) modelling community to correctly describe physico-chemical processes after many years of mainly focusing on biokinetics. Indeed, future modelling needs, such as a plant-wide phosphorus (P) description, require a major...... at different cationic/anionic loads. In this way, the general applicability/flexibility of the proposed approach is demonstrated, by implementing the aqueous phase chemistry module in some of the most frequently used WWTP process simulation models. Finally, it is shown how traditional wastewater modelling...

  19. Selected ion flow tube (SIFT) studies of the reactions of H3O+, NO+ and O-2(+center dot) with six volatile phytogenic esters

    Czech Academy of Sciences Publication Activity Database

    Sovová, K.; Dryahina, Kseniya; Španěl, Patrik

    2011-01-01

    Roč. 300, č. 1 (2011), s. 31-38 ISSN 1387-3806 R&D Projects: GA ČR GA202/09/0800; GA ČR GA203/09/0256 Institutional research plan: CEZ:AV0Z40400503 Keywords : SIFT-MS * ion-molecule reactions * plant esters Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.549, year: 2011

  20. Electron DDCS in ionization of H2O by 72 MeV O8+ ions: comparison with CDW-EIS post and prior forms

    Science.gov (United States)

    Nandi, Saikat; Biswas, S.; Khan, A.; Agnihotri, A. N.; Kasthurirangan, S.; Monti, J. M.; Tachinot, C. A.; Rivarola, R. D.; Misra, D.; Tribedi, Lokesh C.

    2014-04-01

    We have measured energy and angular distributions of double differential cross-sections (DDCS) for electron emission in ionization of water molecule under the impact of 72-MeV O8+ ions. The DDCS values have been compared with a state-of-the-art CDW-EIS calculation for both the prior and post forms of scattering matrix. The prior form of the CDW-EIS model produces better quantitative agreement with the experimental data.