WorldWideScience

Sample records for asymmetric salt ion

  1. Intrinsic potential of cell membranes: opposite effects of lipid transmembrane asymmetry and asymmetric salt ion distribution

    DEFF Research Database (Denmark)

    Gurtovenko, Andrey A; Vattulainen, Ilpo

    2009-01-01

    Using atomic-scale molecular dynamics simulations, we consider the intrinsic cell membrane potential that is found to originate from a subtle interplay between lipid transmembrane asymmetry and the asymmetric distribution of monovalent salt ions on the two sides of the cell membrane. It turns out...... that both the asymmetric distribution of phosphatidylcholine (PC) and phosphatidylethanolamine (PE) lipids across a membrane and the asymmetric distribution of NaCl and KCl induce nonzero drops in the transmembrane potential. However, these potential drops are opposite in sign. As the PC leaflet faces...

  2. Asymmetric ion trap

    International Nuclear Information System (INIS)

    An ion trap having two end cap electrodes disposed asymmetrically about a center of a ring electrode is disclosed. The inner surface of the end cap electrodes are conformed to an asymmetric pair of equipotential lines of the harmonic formed by the application of voltages to the electrodes. The asymmetry of the end cap electrodes allows ejection of charged species through the closer of the two electrodes which in turn allows for simultaneously detecting anions and cations expelled from the ion trap through the use of two detectors charged with opposite polarity. 4 figs

  3. Salt supply to and significance of asymmetric salt diapirs

    DEFF Research Database (Denmark)

    Koyi, H.; Burliga, S.; Chemia, Zurab

    2012-01-01

    Salt diapirs can be asymmetric both internally and externally reflecting their evolution history. As such, this asymmetry bear a significant amount of information about the differential loading (± lateral forces) and in turn the salt supply that have shaped the diapir. In two dimensions, In this...... southeastern overhang due to salt extrusion during Middle Cretaceous followed by its burial in Tertiary. This external asymmetry is also reflected in the internal configuration of the diapir which shows different rates of salt flow on the two halves of the structure. The asymmetric external and internal...

  4. Asymmetric Hydrogenation of 3-Substituted Pyridinium Salts.

    Science.gov (United States)

    Renom-Carrasco, Marc; Gajewski, Piotr; Pignataro, Luca; de Vries, Johannes G; Piarulli, Umberto; Gennari, Cesare; Lefort, Laurent

    2016-07-01

    The use of an equivalent amount of an organic base leads to high enantiomeric excess in the asymmetric hydrogenation of N-benzylated 3-substituted pyridinium salts into the corresponding piperidines. Indeed, in the presence of Et3 N, a Rh-JosiPhos catalyst reduced a range of pyridinium salts with ee values up to 90 %. The role of the base was elucidated with a mechanistic study involving the isolation of the various reaction intermediates and isotopic labeling experiments. Additionally, this study provided some evidence for an enantiodetermining step involving a dihydropyridine intermediate. PMID:27140832

  5. Room Temperature ionic liquids based on asymmetric ammonium salts

    OpenAIRE

    Shaheen, Sobia

    2013-01-01

    Ionic liquids, ILs, in principle, are salts composed of weakly coordinating ions which are liquids at low temperature (˂100 0C). Room temperature ionic liquids, RTILs are those salts which are liquid even at room temperature. Due to the unique properties, such as large liquid range, negligible vapour pressure, solubility of wide range of materials and potential to be recycled and reused, ILs have become a popular class of solvents and catalysts.This study reports the synthesis of a library of...

  6. Solitary waves in asymmetric electron-positron-ion plasmas

    Science.gov (United States)

    Lu, Ding; Li, Zi-Liang; Xie, Bai-Song

    2015-10-01

    > By solving the coupled equations of the electromagnetic field and electrostatic potential, we investigate solitary waves in an asymmetric electron-positron plasma and/or electron-positron-ion plasmas with delicate features. It is found that the solutions of the coupled equations can capture multipeak structures of solitary waves in the case of cold plasma, which are left out by using the long-wavelength approximation. By considering the effect of ion motion with respect to non-relativistic and ultra-relativistic temperature plasmas, we find that the ions' mobility can lead to larger-amplitude solitary waves; especially, this becomes more obvious for a high-temperature plasma. The effects of asymmetric temperature between electrons and positrons and the ion fraction on the solitary waves are also studied and presented. It is shown that the amplitudes of solitary waves decrease with positron temperature in asymmetric temperature electron-positron plasmas and decrease also with ion concentration.

  7. Study of flow in asymmetric heavy-ion collisions

    International Nuclear Information System (INIS)

    Azimuthal anisotropy is a key tool to study the strongly interacting medium produced in relativistic heavy ion collisions. This observable is sensitive to the equation of state of the system formed in the heavy-ion collisions. Recently, it has been proposed at the Relativistic Heavy Ion Collider, to carry out a program of asymmetric heavy-ion collisions. Among other physics possibilities, it is believed to provide insight on the initial conditions through study of event-by-event fluctuation in the measure of the azimuthal anisotropy. Knowing the initial condition is vital for any theoretical calculations in relativistic heavy-ion collisions

  8. Elliptic and triangular flow in asymmetric heavy-ion collisions

    International Nuclear Information System (INIS)

    We present a study of the elliptic (v2) and triangular (v3) flow and their corresponding eccentricity fluctuations for asymmetric (Au+Ag, Au+Cu, and Au+Si) collisions at √(sNN) = 200 GeV. These are compared to the corresponding results from symmetric (Au+Au and Cu+Cu) collisions at the same energy. The study which is carried out using a multiphase transport (AMPT) model shows that triangularity (ε3), fluctuations in triangularity and v3 do not show much variation for the different colliding ion sizes studied. However the eccentricity (ε2), fluctuations in eccentricity and v2, shows a strong dependence on colliding ion size for a given number of participating nucleons. Our study thus indicates that asymmetric heavy-ion collisions could be used to constrain models dealing with flow fluctuations in heavy-ion collisions.

  9. Elliptic and Triangular flow in asymmetric heavy-ion collisions

    CERN Document Server

    Haque, Md Rihan; Mohanty, Bedangadas

    2011-01-01

    We present a study of the elliptic (v2) and triangular (v3) flow and their corresponding eccentricity fluctuations for asymmetric (Au+Ag, Au+Cu and Au+Si) collisions at \\sqrt_NN = 200 GeV. These are compared to the corresponding results from symmetric (Au+Au and Cu+Cu) collisions at the same energy. The study which is carried out using a multi-phase transport (AMPT) model shows that triangularity (\\epsilon_3), fluctuations in triangularity and v3 do not show much variation for the different colliding ion sizes studied. However the eccentricity (\\epsilon_2), fluctuations in eccentricity and v2 shows a strong dependence on colliding ion size for a given number of participating nucleons. Our study thus indicates that asymmetric heavy-ion collisions could be used to constrain models dealing with flow fluctuations in heavy-ion collisions.

  10. Ion pumping in nanochannels using an asymmetric electrode array

    OpenAIRE

    Sparreboom, W.; Cucu, C.F.; Eijkel, J.C.T.; Berg, van den, T.J.T.P.; Locascio, L.E.; Gaitan, M.; Paegel, B.M.; Ross, D J; Vreeland, W. N.

    2008-01-01

    We demonstrate an ion pump, consisting of a nanochannel with an AC driven asymmetric electrode array. Our system enables us to actively pump ions using a low driving voltage. In all experiments the electrical double layers are overlapping. Via viscous coupling ion pumping is accompanied by liquid pumping. Actuation below 500 mV at 10 Hz results in a liquid velocity of ~10 μm/s, corresponding to an electrical ion current of ~400 fA. Finite element simulations support the experimental data.

  11. Multicomponent asymmetric reactions mediated by proline lithium salt

    DEFF Research Database (Denmark)

    Renzi, Polyssena; Overgaard, Jacob; Bella, Marco

    2010-01-01

    The multicomponent reaction between proline lithium salt, 2-cyclohexen-1-one and aliphatic aldehydes affords the 4- alkylidene-2-cyclohexen-1-ones, which are interesting fragrances, and bicyclic amino acids that bear four additional stereocenters, obtained as single stereoisomer....

  12. Ion aggregation in high salt solutions. III. Computational vibrational spectroscopy of HDO in aqueous salt solutions.

    Science.gov (United States)

    Choi, Jun-Ho; Kim, Heejae; Kim, Seongheun; Lim, Sohee; Chon, Bonghwan; Cho, Minhaeng

    2015-05-28

    The vibrational frequency, frequency fluctuation dynamics, and transition dipole moment of the O-D stretch mode of HDO molecule in aqueous solutions are strongly dependent on its local electrostatic environment and hydrogen-bond network structure. Therefore, the time-resolved vibrational spectroscopy the O-D stretch mode has been particularly used to investigate specific ion effects on water structure. Despite prolonged efforts to understand the interplay of O-D vibrational dynamics with local water hydrogen-bond network and ion aggregate structures in high salt solutions, still there exists a gap between theory and experiment due to a lack of quantitative model for accurately describing O-D stretch frequency in high salt solutions. To fill this gap, we have performed numerical simulations of Raman scattering and IR absorption spectra of the O-D stretch mode of HDO in highly concentrated NaCl and KSCN solutions and compared them with experimental results. Carrying out extensive quantum chemistry calculations on not only water clusters but also ion-water clusters, we first developed a distributed vibrational solvatochromic charge model for the O-D stretch mode in aqueous salt solutions. Furthermore, the non-Condon effect on the vibrational transition dipole moment of the O-D stretch mode was fully taken into consideration with the charge response kernel that is non-local polarizability density. From the fluctuating O-D stretch mode frequencies and transition dipole vectors obtained from the molecular dynamics simulations, the O-D stretch Raman scattering and IR absorption spectra of HDO in salt solutions could be calculated. The polarization effect on the transition dipole vector of the O-D stretch mode is shown to be important and the asymmetric line shapes of the O-D stretch Raman scattering and IR absorption spectra of HDO especially in highly concentrated NaCl and KSCN solutions are in quantitative agreement with experimental results. We anticipate that this

  13. The Receptacle Model of Salting-In by Tetramethylammonium Ions

    Science.gov (United States)

    Hribar–Lee, Barbara; Dill, Ken A.; Vlachy, Vojko

    2010-01-01

    Water is a poor solvent for nonpolar solutes. Water containing ions is an even poorer solvent. According to standard terminology, the tendency of salts to precipitate oils from water is called salting-out. However, interestingly, some salt ions, such as tetramethylammonium (TMA), cause instead the salting-in of hydrophobic solutes. Even more puzzling, there is a systematic dependence on solute size. TMA causes the salting-out of small hydrophobes and the salting-in of larger nonpolar solutes. We study these effects using NPT Monte Carlo simulations of the MB + dipole model of water, which was previously shown to account for hydrophobic effects and ion solubilities in water. The present model gives a structural interpretation for the thermodynamics of salting-in. The TMA structure allows deep penetration by a first shell of waters, the dipoles of which interact electrostatically with the ion. This first water shell sets up a second water shell that is shaped to act as a receptacle that binds the nonpolar solute. In this way, a nonpolar solute can actually bind more tightly to the TMA ion than to another hydrophobe, leading to the increased solubility and salting-in. Such structuring may also explain why molecular ions do not follow the same charge density series’ as atomic ions do. PMID:21028768

  14. Receptacle model of salting-in by tetramethylammonium ions.

    Science.gov (United States)

    Hribar-Lee, Barbara; Dill, Ken A; Vlachy, Vojko

    2010-11-25

    Water is a poor solvent for nonpolar solutes. Water containing ions is an even poorer solvent. According to standard terminology, the tendency of salts to precipitate oils from water is called salting-out. However, interestingly, some salt ions, such as tetramethylammonium (TMA), cause instead the salting-in of hydrophobic solutes. Even more puzzling, there is a systematic dependence on solute size. TMA causes the salting-out of small hydrophobes and the salting-in of larger nonpolar solutes. We study these effects using NPT Monte Carlo simulations of the Mercedes-Benz (MB) + dipole model of water, which was previously shown to account for hydrophobic effects and ion solubilities in water. The present model gives a structural interpretation for the thermodynamics of salting-in. The TMA structure allows deep penetration by a first shell of waters, the dipoles of which interact electrostatically with the ion. This first water shell sets up a second water shell that is shaped to act as a receptacle that binds the nonpolar solute. In this way, a nonpolar solute can actually bind more tightly to the TMA ion than to another hydrophobe, leading to the increased solubility and salting-in. Such structuring may also explain why molecular ions do not follow the same charge density series as atomic ions do. PMID:21028768

  15. Influence of salt ions on binding to molecularly imprinted polymers.

    OpenAIRE

    Kempe, Henrik; Kempe, Maria

    2010-01-01

    Salt ions were found to have an influence on template binding to two model molecularly imprinted polymers (MIPs), targeted to penicillin G and propranolol, respectively, in water-acetonitrile mixtures. Water was detrimental to rebinding of penicillin G whereas propranolol bound in the entire water-acetonitrile range tested. In 100% aqueous solution, 3-M salt solutions augmented the binding of both templates. The effects followed the Hofmeister series with kosmotropic ions promoting the larges...

  16. Hypertension: Salt restriction, sodium homeostasis, and other ions

    OpenAIRE

    Neeru Gupta; Kishan Kumar Jani; Nivedita Gupta

    2011-01-01

    Salt is composed of Sodium Chloride (NaCl) which in body water becomes essential electrolytes, viz., Sodium (Na >+ ) and Chloride (Cl >- ) ions, including in the blood and other extracellular fluids (ECF). Na >+ ions are necessary cations in muscle contractions and their depletion will effect all the muscles in body including smooth muscle contraction of blood vessels, a fact which is utilized in lowering the blood pressure. Na+ ions also hold water with them in the ECF. Na >+ homeostasis in ...

  17. Mitochondrial membranes with mono- and divalent salt: changes induced by salt ions on structure and dynamics

    DEFF Research Database (Denmark)

    Pöyry, Sanja; Róg, Tomasz; Karttunen, Mikko;

    2009-01-01

    membrane electrostatic potential. The changes induced by salt are more prominent in dynamical properties related to ion binding and formation of ion-lipid complexes and lipid aggregates, as rotational diffusion of lipids is slowed down by ions, especially in the case of CaCl(2). In the same spirit, lateral...... diffusion of lipids is slowed down rather considerably for increasing concentration of CaCl(2). Both findings for dynamic properties can be traced to the binding of ions with lipid head groups and the related changes in interaction patterns in the headgroup region, where the binding of Na(+) and Ca(2+) ions...

  18. Ion flux profiles and plant ion homeostasis control under salt stress

    OpenAIRE

    Sun, Jian; Chen, Shao-Liang; Dai, Song-Xiang; Wang, Rui-gang; Li, Ni-Ya; Shen, Xin; Zhou, Xiao-Yang; Lu, Cun-Fu; Zheng, Xiao-Jiang; Hu, Zan-Min; Zhang, Zeng-Kai; Song, Jin; Xu, Yue

    2009-01-01

    The ability of a plant to maintain an ionic homeostasis is crucial in plant salt tolerance. Direct evidence based on data from the non-invasive measurement of ion fluxes would not only offer new insight about the function of the transporter but also provide a whole plant approach for dissecting salt adaptation mechanisms. Here, we review some reports using the ion-selective microelectrodes to characterize the net ion fluxes of tissues or cells.

  19. The speciation of actinide ions in concentrated salt solutions

    International Nuclear Information System (INIS)

    Many separations of actinide ions involve concentrated solutions. There is additional interest in actinide behavior in brine solutions in the WIPP salt repository. Unfortunately, little understanding exists on the speciation of actinides in concentrated solutions. The author has studied the extraction distribution of Am(III) as a function of concentration of NX salts (N-, Li+, Na+, K+, NH4+ and X = ClO4-, Cl-, NO3-). Analyses of the distribution curves are discussed in terms of hydration, complexation, etc. effects on the Am(III). The variation of the calculated stability constants with ionic strength is compared with the expected variation using Specific-Ion Interaction Theory (SIT)

  20. Hypertension: Salt restriction, sodium homeostasis, and other ions

    Directory of Open Access Journals (Sweden)

    Neeru Gupta

    2011-01-01

    Full Text Available Salt is composed of Sodium Chloride (NaCl which in body water becomes essential electrolytes, viz., Sodium (Na >+ and Chloride (Cl >- ions, including in the blood and other extracellular fluids (ECF. Na >+ ions are necessary cations in muscle contractions and their depletion will effect all the muscles in body including smooth muscle contraction of blood vessels, a fact which is utilized in lowering the blood pressure. Na+ ions also hold water with them in the ECF. Na >+ homeostasis in body is maintained by thirst (water intake, kidneys (urinary excretion and skin (sweating. In Na >+ withdrawal, body tries to maintain homeostasis as far as possible. However, in certain conditions (e.g., during exercise, intake of drugs and in disorders causing Syndrome of Inappropriate Anti Diuretic Hormone Secretion (SIADH, diuretics, diarrhea coupled with moderate or severe dietary salt restriction (anorexia nervosa, hyponatremia can get precipitated. Hyponatremia is one end point in the spectrum of disorders caused by severe Na >+ depletion whereas in moderate depletion it can cause hypohydration (or less total body water and lower urinary volume (U v . Moreover, salt sensitivity varies in various populations leading to different responses in relation to dietary Na >+ intake. Diabetes and Hypertension often co-exist but Na >+ withdrawal in salt sensitive subjects worsens diabetes though hypertension gets better and reverse occurs in salt loading. Therefore, Na >+ or salt restriction may be non-physiological. In hypertensive subjects other alternatives to Na >+ withdrawal could be Potassium (K >+ and Calcium (Ca >2+ supplementation. Further studies are required to monitor safety/side effects of salt restriction.

  1. Hypertension: salt restriction, sodium homeostasis, and other ions.

    Science.gov (United States)

    Gupta, Neeru; Jani, Kishan Kumar; Gupta, Nivedita

    2011-03-01

    Salt is composed of Sodium Chloride (NaCl) which in body water becomes essential electrolytes, viz., Sodium (Na⁺) and Chloride (Cl⁻) ions, including in the blood and other extracellular fluids (ECF). Na⁺ ions are necessary cations in muscle contractions and their depletion will effect all the muscles in body including smooth muscle contraction of blood vessels, a fact which is utilized in lowering the blood pressure. Na⁺ ions also hold water with them in the ECF. Na⁺ homeostasis in body is maintained by thirst (water intake), kidneys (urinary excretion) and skin (sweating). In Na⁺ withdrawal, body tries to maintain homeostasis as far as possible. However, in certain conditions (e.g., during exercise, intake of drugs and in disorders causing Syndrome of Inappropriate Anti Diuretic Hormone Secretion (SIADH), diuretics, diarrhea) coupled with moderate or severe dietary salt restriction (anorexia nervosa), hyponatremia can get precipitated. Hyponatremia is one end point in the spectrum of disorders caused by severe Na⁺ depletion whereas in moderate depletion it can cause hypohydration (or less total body water) and lower urinary volume (U v ). Moreover, salt sensitivity varies in various populations leading to different responses in relation to dietary Na⁺ intake. Diabetes and Hypertension often co-exist but Na⁺ withdrawal in salt sensitive subjects worsens diabetes though hypertension gets better and reverse occurs in salt loading. Therefore, Na⁺ or salt restriction may be non-physiological. In hypertensive subjects other alternatives to Na⁺ withdrawal could be Potassium (K⁺) and Calcium (Ca⁺²) supplementation. Further studies are required to monitor safety/side effects of salt restriction. PMID:23250294

  2. Surface segregation of dissolved salt ions

    Czech Academy of Sciences Publication Activity Database

    Höfft, O.; Borodin, A.; Kahnert, U.; Kempter, V.; Dang, L. X.; Jungwirth, Pavel

    2006-01-01

    Roč. 110, č. 24, (2006), s. 11971-11976. ISSN 1520-6106 R&D Projects: GA MŠk(CZ) LC512; GA MŠk(CZ) ME 644 Grant ostatní: NSF(US) CHE0431312; NSF(US) CHE0209719 Institutional research plan: CEZ:AV0Z40550506 Keywords : MIES spectroscopy * molecular dynamics * ion solvation Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.115, year: 2006

  3. Capillary Ion Concentration Polarization for Power-Free Salt Purification

    Science.gov (United States)

    Park, Sungmin; Jung, Yeonsu; Cho, Inhee; Kim, Ho-Young; Kim, Sung Jae

    2014-11-01

    In this presentation, we experimentally and theoretically demonstrated the capillary based ion concentration polarization for power-free salt purification system. Traditional ion concentration polarization phenomenon has been studied for a decade for both fundamental nanoscale fluid dynamics and novel engineering applications such as desalination, preconcentration and energy harvesting devices. While the conventional system utilizes an external power source, the system based on capillary ion concentration polarization is capable of perm-selective ion transportation only by capillarity so that the same ion depletion zone can be formed without any external power sources. An ion concentration profile near the nanostructure was tracked using fluorescent probes and analyzed by solving the modified Nernst-Planck equation. As a result, the concentration in the vicinity of the nanostructure was at least 10 times lower than that of bulk electrolyte and thus, the liquid absorbed into the nanostructure had the low concentration. This mechanism can be used for the power free salt purification system which would be significantly useful in underdeveloped and remote area. This work was supported by Samsung Research Funding Center of Samsung Electronics under Project Number SRFC-MA1301-02.

  4. Electrodialysis-ion exchange for the separation of dissolved salts

    International Nuclear Information System (INIS)

    The Department of Energy generates and stores a significant quantity of low level, high level, and mixed wastes. As some of the DOE facilities are decontaminated and decommissioned, additional and possibly different forms of wastes will be generated. A significant portion of these wastes are aqueous streams containing acids, bases, and salts, or are wet solids containing inorganic salts. Some of these wastes are quite dilute solutions, whereas others contain large quantities of nitrates either in the form of dissolved salts or acids. Many of the wastes are also contaminated with heavy metals, radioactive products, or organics. Some of these wastes are in storage because a satisfactory treatment and disposal processes have not been developed. This report describes the process of electrodialysis-ion exchange (EDIX) for treating aqueous wastes streams consisting of nitrates, sodium, organics, heavy metals, and radioactive species

  5. Electrodialysis-ion exchange for the separation of dissolved salts

    Energy Technology Data Exchange (ETDEWEB)

    Baroch, C.J. [Wastren, Inc., Westminster, CO (United States); Grant, P.J. [Wastren, Inc., Hummelstown, PA (United States)

    1995-10-01

    The Department of Energy generates and stores a significant quantity of low level, high level, and mixed wastes. As some of the DOE facilities are decontaminated and decommissioned, additional and possibly different forms of wastes will be generated. A significant portion of these wastes are aqueous streams containing acids, bases, and salts, or are wet solids containing inorganic salts. Some of these wastes are quite dilute solutions, whereas others contain large quantities of nitrates either in the form of dissolved salts or acids. Many of the wastes are also contaminated with heavy metals, radioactive products, or organics. Some of these wastes are in storage because a satisfactory treatment and disposal processes have not been developed. There is considerable interest in developing processes that remove or destroy the nitrate wastes. Electrodialysis-Ion Exchange (EDIX) is a possible process that should be more cost effective in treating aqueous waste steams. This report describes the EDIX process.

  6. Peculiarities of mechanizm of sorption of metal ions on salts of heteropolyacids

    International Nuclear Information System (INIS)

    Literary data on sorption properties of low-soluble salts of heteropolyacids (HPA) are considered. A classification of ions, sorbed on HPA salts, is suggested on the basis of modern views on the structure of HPA salts and of the tendency of ions to form heteropolycompounds. Peculiarities of sorption mechanism of certain ion groups are discussed. It is shown that the processes of sorption on HPA salts are of a complex character and they determined by such properties as radius ion potential, ion state in solution, tendency to complexing. The sorption of ions, able to form heteropolycompounds is a multistage process, accompanied by the interaction of ions sorbed with molybdophosphate anion

  7. Ion track symmetric and asymmetric nanopores in polyethylene terephthalate foils for versatile applications

    Science.gov (United States)

    Apel, P. Yu.; Blonskaya, I. V.; Dmitriev, S. N.; Orelovich, O. L.; Sartowska, B. A.

    2015-12-01

    In this report we present several fabrication methods which allow production of ion track nanopore membranes with different pore configurations. Polymer foils, typically polyethylene terephthalate with a thickness of 5-23 μm, are irradiated with accelerated heavy ions (energy of 1-10 MeV/u) and then subjected to different physico-chemical treatments. Depending on the procedure, symmetric or asymmetric pores with nanoscale-sized narrowing are obtained. The asymmetric configurations include conical, funnel-like and bullet-like shapes. In electrolyte solutions the asymmetric nanopores exhibit diode-like properties which strongly depend on the pore shape. The peculiar features of such pores provide a basis for various applications.

  8. Enhanced Salt Removal by Unipolar Ion Conduction in Ion Concentration Polarization Desalination

    Science.gov (United States)

    Kwak, Rhokyun; Pham, Van Sang; Kim, Bumjoo; Chen, Lan; Han, Jongyoon

    2016-05-01

    Chloride ion, the majority salt in nature, is ∼52% faster than sodium ion (DNa+ = 1.33, DCl‑ = 2.03[10‑9m2s‑1]). Yet, current electrochemical desalination technologies (e.g. electrodialysis) rely on bipolar ion conduction, removing one pair of the cation and the anion simultaneously. Here, we demonstrate that novel ion concentration polarization desalination can enhance salt removal under a given current by implementing unipolar ion conduction: conducting only cations (or anions) with the unipolar ion exchange membrane stack. Combining theoretical analysis, experiment, and numerical modeling, we elucidate that this enhanced salt removal can shift current utilization (ratio between desalted ions and ions conducted through electrodes) and corresponding energy efficiency by the factor ∼(D‑ ‑ D+)/(D‑ + D+). Specifically for desalting NaCl, this enhancement of unipolar cation conduction saves power consumption by ∼50% in overlimiting regime, compared with conventional electrodialysis. Recognizing and utilizing differences between unipolar and bipolar ion conductions have significant implications not only on electromembrane desalination, but also energy harvesting applications (e.g. reverse electrodialysis).

  9. Enhanced Salt Removal by Unipolar Ion Conduction in Ion Concentration Polarization Desalination

    Science.gov (United States)

    Kwak, Rhokyun; Pham, Van Sang; Kim, Bumjoo; Chen, Lan; Han, Jongyoon

    2016-01-01

    Chloride ion, the majority salt in nature, is ∼52% faster than sodium ion (DNa+ = 1.33, DCl− = 2.03[10−9m2s−1]). Yet, current electrochemical desalination technologies (e.g. electrodialysis) rely on bipolar ion conduction, removing one pair of the cation and the anion simultaneously. Here, we demonstrate that novel ion concentration polarization desalination can enhance salt removal under a given current by implementing unipolar ion conduction: conducting only cations (or anions) with the unipolar ion exchange membrane stack. Combining theoretical analysis, experiment, and numerical modeling, we elucidate that this enhanced salt removal can shift current utilization (ratio between desalted ions and ions conducted through electrodes) and corresponding energy efficiency by the factor ∼(D− − D+)/(D− + D+). Specifically for desalting NaCl, this enhancement of unipolar cation conduction saves power consumption by ∼50% in overlimiting regime, compared with conventional electrodialysis. Recognizing and utilizing differences between unipolar and bipolar ion conductions have significant implications not only on electromembrane desalination, but also energy harvesting applications (e.g. reverse electrodialysis). PMID:27158057

  10. Enhanced Salt Removal by Unipolar Ion Conduction in Ion Concentration Polarization Desalination.

    Science.gov (United States)

    Kwak, Rhokyun; Pham, Van Sang; Kim, Bumjoo; Chen, Lan; Han, Jongyoon

    2016-01-01

    Chloride ion, the majority salt in nature, is ∼52% faster than sodium ion (DNa+ = 1.33, DCl- = 2.03[10(-9)m(2)s(-1)]). Yet, current electrochemical desalination technologies (e.g. electrodialysis) rely on bipolar ion conduction, removing one pair of the cation and the anion simultaneously. Here, we demonstrate that novel ion concentration polarization desalination can enhance salt removal under a given current by implementing unipolar ion conduction: conducting only cations (or anions) with the unipolar ion exchange membrane stack. Combining theoretical analysis, experiment, and numerical modeling, we elucidate that this enhanced salt removal can shift current utilization (ratio between desalted ions and ions conducted through electrodes) and corresponding energy efficiency by the factor ∼(D- - D+)/(D- + D+). Specifically for desalting NaCl, this enhancement of unipolar cation conduction saves power consumption by ∼50% in overlimiting regime, compared with conventional electrodialysis. Recognizing and utilizing differences between unipolar and bipolar ion conductions have significant implications not only on electromembrane desalination, but also energy harvesting applications (e.g. reverse electrodialysis). PMID:27158057

  11. Simultaneous measurements of plasma flow and ion temperature using the asymmetric double probe

    International Nuclear Information System (INIS)

    The asymmetric double probe method is extended to measure not only the ion temperature but also plasma flow in the tokamak edge plasma under a strong magnetic field. The plasma flow or the Mach number is determined by the ratio of ion saturation currents of the double probe pins, where the axes of the cylindrical pins are oriented perpendicular to the magnetic field and face up-or downstream. An experiment was performed in the JFT-2M tokamak. (author)

  12. An inversion-asymmetric source function for HBT analysis in relativistic heavy ion collisions

    OpenAIRE

    Lianshou, Liu; Shusu, Shi; Jiaxin, Du

    2006-01-01

    The inversion-asymmetry of the emission source in relativistic heavy ion collision under the Bertsch-Pratt convention is discussed and explicitly exhibited by a Monte Carlo model. The Gaussian source function popularly used in the HBT analysis of relativistic heavy ion collisions is invalid in this case. An inversion-asymmetric source function is suggested. A method for extracting the inversion-asymmetry degree of the source together with the source size from experimental data is proposed.

  13. Asymmetric dynamics of ion channel forming proteins - Hepatitis C virus (HCV) p7 bundles.

    Science.gov (United States)

    Kalita, Monoj Mon; Fischer, Wolfgang B

    2016-07-01

    Protein p7 of hepatitis C virus (HCV) is a short 63 amino acid membrane protein which homo-oligomerises in the lipid membrane to form ion and proton conducting bundles. Two different genotypes (GTs) of p7, 1a and 5a, are used to simulate hexameric bundles of the protein embedded in a fully hydrated lipid bilayer during 400ns molecular dynamics (MD) simulations. Whilst the bundle of GT 1a is based on a fully computational derived structure, the bundle of GT 5a is based on NMR spectroscopic data. Results of a full correlation analysis (FCA) reveal that albeit structural differences both bundles screen local minima during the simulation. The collective motion of the protein domains is asymmetric. No 'breathing-mode'-like dynamics is observed. The presence of divalent ions, such as Ca-ions affects the dynamics of especially solvent exposed parts of the protein, but leaves the asymmetric domain motion unaffected. PMID:27079148

  14. Counter-ions between or at asymmetrically charged walls: 2D free-fermion point

    OpenAIRE

    Samaj, L.; Trizac, E.

    2014-01-01

    This work contributes to the problem of determining effective interaction between asymmetrically (likely or oppositely) charged objects whose total charge is neutralized by mobile pointlike counter-ions of the same charge, the whole system being in thermal equilibrium. The problem is formulated in two spatial dimensions with logarithmic Coulomb interactions. The charged objects correspond to two parallel lines at distance d, with fixed line charge densities. Two versions of the model are cons...

  15. Generation of circularly polarized attosecond pulses by intense ultrashort laser pulses from extended asymmetric molecular ions

    Science.gov (United States)

    Yuan, Kai-Jun; Bandrauk, André D.

    2011-08-01

    We present a method for generation of single circularly polarized attosecond pulses in extended asymmetric HHe2+ molecular ions. By employing an intense ultrashort circularly polarized laser pulse with intensity 4.0×1014 W/cm2, wavelength 400 nm, and duration 10 optical cycles, molecular high-order-harmonic generation (MHOHG) spectra with multiple plateaus exhibit characters of circular polarization. Using a classical laser-induced collision model, double collisions of continuum electrons first with neighboring ions and then second with parent ions are presented at a particular internuclear distance and confirmed from numerical solutions of a time-dependent Schrödinger equation. We analyze the MHOHG spectra with a Gabor time window and find that, due to the asymmetry of HHe2+, a single collision trajectory of continuum electrons with ions can produce circularly polarized harmonics, leading to single circularly polarized attosecond pulses for specific internuclear distances.

  16. Generation of circularly polarized attosecond pulses by intense ultrashort laser pulses from extended asymmetric molecular ions

    International Nuclear Information System (INIS)

    We present a method for generation of single circularly polarized attosecond pulses in extended asymmetric HHe2+ molecular ions. By employing an intense ultrashort circularly polarized laser pulse with intensity 4.0x1014 W/cm2, wavelength 400 nm, and duration 10 optical cycles, molecular high-order-harmonic generation (MHOHG) spectra with multiple plateaus exhibit characters of circular polarization. Using a classical laser-induced collision model, double collisions of continuum electrons first with neighboring ions and then second with parent ions are presented at a particular internuclear distance and confirmed from numerical solutions of a time-dependent Schroedinger equation. We analyze the MHOHG spectra with a Gabor time window and find that, due to the asymmetry of HHe2+, a single collision trajectory of continuum electrons with ions can produce circularly polarized harmonics, leading to single circularly polarized attosecond pulses for specific internuclear distances.

  17. Generation of circularly polarized attosecond pulses by intense ultrashort laser pulses from extended asymmetric molecular ions

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Kai-Jun; Bandrauk, Andre D. [Laboratoire de Chimie Theorique, Faculte des Sciences, Universite de Sherbrooke, Sherbrooke, Quebec, J1K 2R1 (Canada)

    2011-08-15

    We present a method for generation of single circularly polarized attosecond pulses in extended asymmetric HHe{sup 2+} molecular ions. By employing an intense ultrashort circularly polarized laser pulse with intensity 4.0x10{sup 14} W/cm{sup 2}, wavelength 400 nm, and duration 10 optical cycles, molecular high-order-harmonic generation (MHOHG) spectra with multiple plateaus exhibit characters of circular polarization. Using a classical laser-induced collision model, double collisions of continuum electrons first with neighboring ions and then second with parent ions are presented at a particular internuclear distance and confirmed from numerical solutions of a time-dependent Schroedinger equation. We analyze the MHOHG spectra with a Gabor time window and find that, due to the asymmetry of HHe{sup 2+}, a single collision trajectory of continuum electrons with ions can produce circularly polarized harmonics, leading to single circularly polarized attosecond pulses for specific internuclear distances.

  18. Structure, Ion Transport, and Rheology of Nanoparticle Salts

    KAUST Repository

    Wen, Yu Ho

    2014-07-08

    Above a critical surface chemistry-dependent particle loading associated with nanoscale interparticle spacing, ligand-ligand interactions-both electrostatic and steric-come into play and govern the structure and dynamics of charged oligomer-functionalized nanoparticle suspensions. We report in particular on the structure, ion transport, and rheology of suspensions of nanoparticle salts created by cofunctionalization of silica particles with tethered sulfonate salts and oligomers. Dispersion of the hairy ionic particles into medium and high dielectric constant liquids yields electrolytes with unique structure and transport properties. We find that electrostatic repulsion imparted by ion dissociation can be tuned to control the dispersion state and rheology through counterion size (i.e., Li+, Na+, and K+) and dielectric properties of the dispersing medium. Analysis of small-angle X-ray scattering (SAXS) structure factors and the mechanical modulus shows that when the interparticle spacing approaches nanometer dimensions, weakly entangled anchored ligands experience strong and long-lived topological constraints analogous to those normally found in well-entangled polymeric fluids. This finding provides insight into the molecular origins of the surprisingly similar rubbery plateau moduli observed in hairy nanoparticle suspensions and entangled polymers of the same chemistry as the tethered ligands. Additionally, we find that a time-composition superposition (TCS) principle exists for the suspensions, which can be used to substantially extend the observation time over which dynamics are observed in jammed, soft glassy suspensions. Application of TCS reveals dynamical similarities between the suspensions and entangled solutions of linear polymer chains; i.e., a hairy particle trapped in a cage appears to exhibit analogous dynamics to a long polymer chain confined to a tube. © 2014 American Chemical Society.

  19. Static and dynamic properties of Rochelle salt considering asymmetric double well potential and anharmonic lattice vibrations

    International Nuclear Information System (INIS)

    The interesting features of phase transition in Rochelle Salt (RS) or C4H4O6NaK.4(H2O) i.e. the appearance of two Curie points Tsub(c1) (255 K) and Tsub(c2) (297 K) and large isotope effect on Tsub(c) are studied. On deuteration the lower Curie point shifts towards lower temperature and the upper Curie point towards the higher temperature, showing evidently the important role played by the hydrogen atoms in the ferroelectric behaviour of RS. A conclusion has finally been drawn from the present and previous investigations that both proton-lattice and phonon-phonon interactions play a vital role in the phase transition in hydrogen bonded ferroelectrics including KDP family and the present Rochelle Salt group. An estimation of the anharmonic contribution in the dynamic and static properties has also been found out for these crystals. (K.B.)

  20. Quarternary Ammonium Salts as Reaction Media for Asymmetric Hydrogenation of Ketoesters

    Czech Academy of Sciences Publication Activity Database

    Floriš, T.; Klusoň, Petr; Bartek, L.; Drobek, M.

    -: -, 2008 - (Baxter, D.; Bay, B.), P44 ISBN N. [ Green Solvents - Progress in Science and Application. Friedrichshafen (DE), 28.09.2008-01.10.2008] R&D Projects: GA ČR GD203/08/H032; GA AV ČR KAN400720701; GA MŠk 1M0577 Institutional research plan: CEZ:AV0Z40720504 Keywords : hydrogenation of ketoesters * ammonium salts Subject RIV: CI - Industrial Chemistry, Chemical Engineering https://ssl.dechema.de/gspsa.html

  1. Estimation of electric conductivity of the quark gluon plasma via asymmetric heavy-ion collisions

    OpenAIRE

    Hirono, Yuji(Department of Physics, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan); Hongo, Masaru; Hirano, Tetsufumi

    2012-01-01

    We show that in asymmetric heavy-ion collisions, especially off-central Cu+Au collisions, a sizable strength of electric field directed from Au nucleus to Cu nucleus is generated in the overlapping region, because of the difference in the number of electric charges between the two nuclei. This electric field would induce an electric current in the matter created after the collision, which result in a dipole deformation of the charge distribution. The directed flow parameters $v_1^{\\pm}$ of ch...

  2. Analysis of triazines and associated metabolites with electrospray ionization field-asymmetric ion mobility spectrometry/mass spectrometry

    DEFF Research Database (Denmark)

    Mie, Axel; Sandulescu, Madaline; Mathiasson, Lennart; Emnéus, Jenny; Reimann, Curt

    2008-01-01

    analysis of triazines. More specifically, we studied the background reduction and sensitivity enhancement that result from the use of a new interface technique, field-asymmetric ion mobility spectrometry (FAIMS), in conjunction with electrospray ionization ion-trap mass spectrometry. This technique allows...

  3. DSC characterization of ion beam modifications in ion conducting PEO-salt polymers

    International Nuclear Information System (INIS)

    Ion conducting polymer films have been prepared by complexing non-conducting poly-(ethylene-oxide), PEO, with x fraction of NH4ClO4 salt. Since its electrical conductivity showed a maximum at x somewhere between 0.18 and 0.19, such polymer films having 17 and 19 wt% salt, have been chosen and irradiated by 160 MeV Ne6+ beam. The films have been investigated by differential scanning calorimetry (DSC) and ac impedance spectroscopy before and after the irradiations. Irradiation-induced shift of an endotherm in our DSC indicates a rise in the melting temperature from 54.6 oC to 57.9 oC for the 19% film. Cross-linking by the Ne-irradiation making the polymer structure more rigid can explain this as well as our other observation of a decrease in electrical conductivity

  4. Ion aggregation in high salt solutions. V. Graph entropy analyses of ion aggregate structure and water hydrogen bonding network

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2016-05-01

    Dissolved ions in water tend to form polydisperse ion aggregates such as ion pairs, relatively compact ion clusters, and even spatially extended ion networks with increasing salt concentration. Combining molecular dynamics simulation and graph theoretical analysis methods, we recently studied morphological structures of ion aggregates with distinctively different characteristics. They can be distinguished from each other by calculating various spectral graph theoretical properties such as eigenvalues and eigenvectors of adjacency matrices of ion aggregates and water hydrogen-bonding networks, minimum path lengths, clustering coefficients, and degree distributions. Here, we focus on percolation and graph entropic properties of ion aggregates and water hydrogen-bonding networks in high salt solutions. Ion network-forming K+ and SCN- ions at high concentrations show a percolating behavior in their aqueous solutions, but ion cluster-forming ions in NaCl solutions do not show such a transition from isolated ion aggregates to percolating ion-water mixture morphology. Despite that the ion aggregate structures are strikingly different for either cluster- or network-forming ions in high salt solutions, it is interesting that the water structures remain insensitive to the electrostatic properties, such as charge densities and polydentate properties, of dissolved ions, and morphological structures of water H-bonding networks appear to be highly robust regardless of the nature and concentration of salt. We anticipate that the present graph entropy analysis results would be of use in understanding a variety of anomalous behaviors of interfacial water around biomolecules as well as electric conductivities of high electrolyte solutions.

  5. Secondary emission of negative ions and electrons resulting from electronic sputtering of cesium salts

    International Nuclear Information System (INIS)

    Secondary ion emission of negative ions and electrons from alkali salts bombarded with high energy (9 MeV) Ar+++ is discussed. Quite different features are observed according to the nature of the salt investigated (halide or oxygenated). In the case of cesium, the electron emission from halides is characterized by intense electron showers (several hundred electrons) with narrow distributions in intensity and orientation. Conversely, for oxygenated salts, these distributions are broader, much less intense (one order of magnitude), and the ion emission exhibits an dissymmetry, which has never been observed for inorganics. This last result is interpreted in terms of radiolysis of the oxygenated salt, a process well documented for gamma-ray irradiation, but not yet reported in secondary ion emission. (author) 17 refs.; 10 figs

  6. Polymer-Supported Cinchona Alkaloid-Derived Ammonium Salts as Recoverable Phase-Transfer Catalysts for the Asymmetric Synthesis of α-Amino Acids

    Directory of Open Access Journals (Sweden)

    Carmen Nájera

    2004-04-01

    Full Text Available Alkaloids such as cinchonidine, quinine and N-methylephedrine have been N-alkylated using polymeric benzyl halides or co-polymerized and then N-alkylated, thus affording a series of polymer-supported chiral ammonium salts which have been employed as phase-transfer catalysts in the asymmetric benzylation of an N-(diphenylmethyleneglycine ester. These new polymeric catalysts can be easily recovered by simple filtration after the reaction and reused. The best ee’s were achieved when Merrifield resin-anchored cinchonidinium ammonium salts were employed.

  7. Mathematical modeling of salt-gradient ion-exchange simulated moving bed chromatography for protein separations

    Institute of Scientific and Technical Information of China (English)

    卢建刚

    2004-01-01

    The salt-gradient operation mode used in ion-exchange simulated moving bed chromatography (SMBC) can improve the efficiency of protein separations. A detailed model that takes into account any kind of adsorption/ion-exchange equilibrium, salt gradient, size exclusion, mass transfer resistance, and port periodic switching mechanism, was developed to simulate the complex dynamics. The model predictions were verified by the experimental data on upward and downward gradients for protein separations reported in the literature. All design and operating parameters (number, configuration, length and diameter of columns, particle size, switching period, flow rates of feed, raffinate, desorbent and extract, protein concentrations in feed, different salt concentrations in desorbent and feed) can be chosen correctly by numerical simulation. This model can facilitate the design, operation, optimization, control and scale-up of salt-gradient ion-exchange SMBC for protein separations.

  8. Ion aggregation in high salt solutions. IV. Graph-theoretical analyses of ion aggregate structure and water hydrogen bonding network.

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2015-09-14

    Ions in high salt solutions form a variety of ion aggregates, from ion pairs to clusters and networks. Their influences on water hydrogen bonding (H-bonding) network structures have long been of great interest. Recently, we have shown that the morphological structures of ion aggregates can be analyzed by using a spectral graph analysis theory, where each ion cluster or ion network is represented by a properly defined graph with edges and vertices. Here, to further examine the network properties of ion aggregates and water H-bonding networks in high salt solutions, we consider a few representative graph-theoretical descriptors: clustering coefficient, minimum path length, global efficiency, and degree distribution of ion aggregates. From the molecular dynamics trajectories, these graph theoretical properties of ion aggregates and water structures in NaCl and kosmotropic solutions are calculated and shown to be strongly dependent on the two types of ion aggregate structures, i.e., ion cluster and ion network. Ion clusters in high NaCl solutions exhibit typical behaviors of scale free network. The corresponding graph theoretical properties of ion networks in high KSCN solutions are notably different from those of NaCl ion clusters and furthermore they are very similar to those of water hydrogen-bonding network. The present graph-theoretical analysis results indicate that the high solubility limits of KSCN and other ion-network-forming salts might originate from their ability to form a large scale morphological network that can be intertwined with co-existing water H-bonding network. Furthermore, it is shown that the graph-theoretical properties of water H-bonding network structures do not strongly depend on the nature of dissolved ions nor on the morphological structures of ion aggregates, indicating that water's H-bonding interaction and network-forming capability are highly robust. We anticipate that the present graph-theoretical analysis results of high salt

  9. Potentiometric Sensor for Real-Time Monitoring of Multivalent Ion Concentrations in Molten Salt

    Energy Technology Data Exchange (ETDEWEB)

    Peter A. Zink; Jan-Fong Jue; Brenda E. Serrano; Guy L. Fredrickson; Ben F. Cowan; Steven D. Herrmann; Shelly X. Li

    2010-07-01

    Electrorefining of spent metallic nuclear fuel in high temperature molten salt systems is a core technology in pyroprocessing, which in turn plays a critical role in the development of advanced fuel cycle technologies. In electrorefining, spent nuclear fuel is treated electrochemically in order to effect separations between uranium, noble metals, and active metals, which include the transuranics. The accumulation of active metals in a lithium chloride-potassium chloride (LiCl-KCl) eutectic molten salt electrolyte occurs at the expense of the UCl3-oxidant concentration in the electrolyte, which must be periodically replenished. Our interests lie with the accumulation of active metals in the molten salt electrolyte. The real-time monitoring of actinide concentrations in the molten salt electrolyte is highly desirable for controlling electrochemical operations and assuring materials control and accountancy. However, real-time monitoring is not possible with current methods for sampling and chemical analysis. A new solid-state electrochemical sensor is being developed for real-time monitoring of actinide ion concentrations in a molten salt electrorefiner. The ultimate function of the sensor is to monitor plutonium concentrations during electrorefining operations, but in this work gadolinium was employed as a surrogate material for plutonium. In a parametric study, polycrystalline sodium beta double-prime alumina (Na-ß?-alumina) discs and tubes were subject to vapor-phase exchange with gadolinium ions (Gd3+) using a gadolinium chloride salt (GdCl3) as a precursor to produce gadolinium beta double-prime alumina (Gd-ß?-alumina) samples. Electrochemical impedance spectroscopy and microstructural analysis were performed on the ion-exchanged discs to determine the relationship between ion exchange and Gd3+ ion conductivity. The ion-exchanged tubes were configured as potentiometric sensors in order to monitor real-time Gd3+ ion concentrations in mixtures of gadolinium

  10. Potassium Ions are More Effective than Sodium Ions in Salt Induced Peptide Formation

    Science.gov (United States)

    Dubina, Michael V.; Vyazmin, Sergey Yu.; Boitsov, Vitali M.; Nikolaev, Eugene N.; Popov, Igor A.; Kononikhin, Alexey S.; Eliseev, Igor E.; Natochin, Yuri V.

    2013-04-01

    Prebiotic peptide formation under aqueous conditions in the presence of metal ions is one of the plausible triggers of the emergence of life. The salt-induced peptide formation reaction has been suggested as being prebiotically relevant and was examined for the formation of peptides in NaCl solutions. In previous work we have argued that the first protocell could have emerged in KCl solution. Using HPLC-MS/MS analysis, we found that K+ is more than an order of magnitude more effective in the L-glutamic acid oligomerization with 1,1'-carbonyldiimidazole in aqueous solutions than the same concentration of Na+, which is consistent with the diffusion theory calculations. We anticipate that prebiotic peptides could have formed with K+ as the driving force, not Na+, as commonly believed.

  11. Asymmetric catalytic formation of quaternary carbons by iminium ion trapping of radicals

    Science.gov (United States)

    Murphy, John J.; Bastida, David; Paria, Suva; Fagnoni, Maurizio; Melchiorre, Paolo

    2016-04-01

    An important goal of modern organic chemistry is to develop new catalytic strategies for enantioselective carbon–carbon bond formation that can be used to generate quaternary stereogenic centres. Whereas considerable advances have been achieved by exploiting polar reactivity, radical transformations have been far less successful. This is despite the fact that open-shell intermediates are intrinsically primed for connecting structurally congested carbons, as their reactivity is only marginally affected by steric factors. Here we show how the combination of photoredox and asymmetric organic catalysis enables enantioselective radical conjugate additions to β,β-disubstituted cyclic enones to obtain quaternary carbon stereocentres with high fidelity. Critical to our success was the design of a chiral organic catalyst, containing a redox-active carbazole moiety, that drives the formation of iminium ions and the stereoselective trapping of photochemically generated carbon-centred radicals by means of an electron-relay mechanism. We demonstrate the generality of this organocatalytic radical-trapping strategy with two sets of open-shell intermediates, formed through unrelated light-triggered pathways from readily available substrates and photoredox catalysts—this method represents the application of iminium ion activation (a successful catalytic strategy for enantioselective polar chemistry) within the realm of radical reactivity.

  12. Asymmetric catalytic formation of quaternary carbons by iminium ion trapping of radicals.

    Science.gov (United States)

    Murphy, John J; Bastida, David; Paria, Suva; Fagnoni, Maurizio; Melchiorre, Paolo

    2016-04-14

    An important goal of modern organic chemistry is to develop new catalytic strategies for enantioselective carbon-carbon bond formation that can be used to generate quaternary stereogenic centres. Whereas considerable advances have been achieved by exploiting polar reactivity, radical transformations have been far less successful. This is despite the fact that open-shell intermediates are intrinsically primed for connecting structurally congested carbons, as their reactivity is only marginally affected by steric factors. Here we show how the combination of photoredox and asymmetric organic catalysis enables enantioselective radical conjugate additions to β,β-disubstituted cyclic enones to obtain quaternary carbon stereocentres with high fidelity. Critical to our success was the design of a chiral organic catalyst, containing a redox-active carbazole moiety, that drives the formation of iminium ions and the stereoselective trapping of photochemically generated carbon-centred radicals by means of an electron-relay mechanism. We demonstrate the generality of this organocatalytic radical-trapping strategy with two sets of open-shell intermediates, formed through unrelated light-triggered pathways from readily available substrates and photoredox catalysts--this method represents the application of iminium ion activation (a successful catalytic strategy for enantioselective polar chemistry) within the realm of radical reactivity. PMID:27075098

  13. Scaling of triple differential cross-sections for asymmetric (, 2) process on helium isoelectronic ions by fast electrons

    Indian Academy of Sciences (India)

    M K Srivastava

    2005-01-01

    A simple scaling law is obtained for asymmetric (, 2) process on helium isoelectronic ions by fast electrons. It is based on treating the targets as having one active electron moving in the effective Coulomb field of the atomic core with an effective charge ' = − 5/8. This effective charge is also used in the description of the scattered and ejected electrons. The model has been tested against other available (, 2) results on helium in asymmetric geometry. The scaling law is found to work reasonably well for fast incident electrons and becomes increasingly accurate as target increases.

  14. Regulation of ion homeostasis by aminolevulinic acid in salt-stressed wheat seedlings

    Science.gov (United States)

    Türk, Hülya; Genişel, Mucip; Erdal, Serkan

    2016-04-01

    Salinity is regarded as a worldwide agricultural threat, as it seriously limits plant development and productivity. Salt stress reduces water uptake in plants by disrupting the osmotic balance of soil solution. In addition, it creates a damaged metabolic process by causing ion imbalance in cells. In this study, we aim to examine the negative effects of 5-aminolevulinic acid (ALA) (20 mg/l) on the ion balance in wheat seedling leaves exposed to salt stress (150 mM). Sodium is known to be highly toxic for plant cells at high concentrations, and is significantly increased by salt stress. However, it can be reduced by combined application of ALA and salt, compared to salt application alone. On the other hand, while the K+/Na+ ratio was reduced by salt stress, ALA application changed this ratio in favor of K+. Manganese, iron, and copper were also able to reduce stress. However, ALA pre-treatment resulted in mineral level increments. Conversely, the stress-induced rise in magnesium, potassium, calcium, phosphorus, zinc, and molybdenum were further improved by ALA application. These data clearly show that ALA has an important regulatory effect of ion balance in wheat leaves.

  15. Detection of Potato Storage Disease via Gas Analysis: A Pilot Study Using Field Asymmetric Ion Mobility Spectrometry

    OpenAIRE

    Massimo Rutolo; Covington, James A.; John Clarkson; Daciana Iliescu

    2014-01-01

    Soft rot is a commonly occurring potato tuber disease that each year causes substantial losses to the food industry. Here, we explore the possibility of early detection of the disease via gas/vapor analysis, in a laboratory environment, using a recent technology known as FAIMS (Field Asymmetric Ion Mobility Spectrometry). In this work, tubers were inoculated with a bacterium causing the infection, Pectobacterium carotovorum, and stored within set environmental conditions in order to manage di...

  16. Flotation of uranyl ions by alkylcarboxylic acid salts of potassium

    International Nuclear Information System (INIS)

    Physical and chemical features of uranyl cation flotation by potassium salts of fatty acids from diluted solutions are presented. Maximum degree of uranyl flotation is shown to occur in the range of pH=5-6 which corresponds to flotoactive forms of UO22+(OH)+ and to the form of collector as RCOO-. Efficiency of collector first increases with the length of hydrocarbon radical (due to decreasing sublate solubility) and then declines (due to increasing electrokinetic potential). Increase of the temperature of solutions leads to an increase in sublate solubility and to a decrease in the extent of uranyl flotation. 8 refs.; 4 figs.; 2 tabs

  17. Determining Of Iodide Concentration In Salt Using Iodide Ion Selective Electrode

    International Nuclear Information System (INIS)

    There are various studies about the determination of iodide or iodinate in table salt samples. Iodo metric method (5), spectrophotometric method(8), gravimetric method (2), chromatographic method (6), differential potentiometric method (3).But with ion selective electrode technicality the determination of iodide in geothermal water was only determined. So, in this work, the concentration of iodide in control table salt, iodinate table salt samples were determination, using iodide ion selective electrode . Iodide calibration graph was plotted according to the standard method, and the results of control salt samples which contain a defined concentration of iodide, and known amount of ionic strength adjustment buffer, were compatible with the assigned values. The linearity and sensitivity of method were studied, the results were 50 mg.L-1 and 0.2 mg.L-1 respectively . While, when the method applied on iodinate table salt samples which contain a amount concentration of potassium iodate (KIO3), the results were inconsistent. So, we had to convert the KIO3 to I-1 with oxidation - reduction reaction. By using convenient reduction in acidic medium . Iodate calibration graph was plotted according to the last standard method, and the results of control iodinate table salt samples were good with relative standard deviation was 3 %. (author)

  18. Study of ion-exchange properties of heteropolyacids salts of Ce (IV)

    International Nuclear Information System (INIS)

    Heteropolyacid is communally used in the field of nuclear science and technology for separation of radionuclides, because of the good selectivity for special ions and the high resistance towards ionizing radiation and heating. A new granulated amorphous heteropolyacid salts ion-exchangers. Cerium silicotungstate have been prepared in different conditions (pH, temperature...etc.) showed a good exchange properties and very high selectivity for Pb, Fe (III), Ag, Ba, U and Ra. (author)

  19. Electrokinetic salt removal from porous building materials using ion exchange membranes

    NARCIS (Netherlands)

    Kamran, K.; Van Soestbergen, M.; Pel, L.

    The removal of salt from porous building materials under the influence of an applied voltage gradient normally results in high pH gradients due to the formation of protons and hydroxyl ions at the electrodes. The formed acidic and alkaline regions not only lead to disintegration of the porous materi

  20. Seed Treatment with Auxins Modulates Growth and Ion Partitioning in Salt-stressed Wheat Plants

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Experiments were performed to determine whether seed priming with different concentrations (100, 150, and 200 mg/L) of auxins (indoleacetic acid (IAA), indolebutyric acid (IBA), or their precursor tryptophane (Trp)) could alter salinity induced perturbances in salicylic acid and ion concentrations and, hence, growth in wheat (Triticum aestivum L.) cultivars, namely M.H.-97 (salt intolerant) and Inqlab-91 (salt tolerant). Primed and non-primed seeds were sown in Petri dishes in a growth room, as well as in a field treated with 15 dS/m NaCl salinity. All priming agents, except IBA, increased the final germination percentage in both cultivars. The seedlings of either cultivar raised from Trp-treated seeds had greater dry biomass when under salt stress. In field experiments, Trp priming was much more effective in mediating the increase in grain yield,irrespective of the cultivar, under salt stress. The alleviatory effect of Trp was found to be associated with reduced uptake of Na+ in the roots and subsequent translocation to the shoots, as well as increased partitioning of Ca2+ in the roots of salt-stressed wheat plants. Plants of both cultivars raised from Trp- and IAA-treated seeds accumulated free salicylic acid in their leaves when under salt stress. Overall, the Trp priming-induced improvement in germination and the subsequent growth of wheat plants could be related to ion homeostasis when under salt stress. The possible involvement of salicylic acid in the Trp priming-induced better growth under conditions of salt stress is discussed.

  1. Potentiometric Sensor for Real-Time Monitoring of Multivalent Ion Concentrations in Molten Salt

    International Nuclear Information System (INIS)

    Electrorefining of spent metallic nuclear fuel in high temperature molten salt systems is a core technology in pyroprocessing, which in turn plays a critical role in the development of advanced fuel cycle technologies. In electrorefining, spent nuclear fuel is treated electrochemically in order to effect separations between uranium, noble metals, and active metals, which include the transuranics. The accumulation of active metals in a lithium chloride-potassium chloride (LiCl-KCl) eutectic molten salt electrolyte occurs at the expense of the UCl3-oxidant concentration in the electrolyte, which must be periodically replenished. Our interests lie with the accumulation of active metals in the molten salt electrolyte. The real-time monitoring of actinide concentrations in the molten salt electrolyte is highly desirable for controlling electrochemical operations and assuring materials control and accountancy. However, real-time monitoring is not possible with current methods for sampling and chemical analysis. A new solid-state electrochemical sensor is being developed for real-time monitoring of actinide ion concentrations in a molten salt electrorefiner. The ultimate function of the sensor is to monitor plutonium concentrations during electrorefining operations, but in this work gadolinium was employed as a surrogate material for plutonium. In a parametric study, polycrystalline sodium beta double-prime alumina (Na-β(doubleprime)-alumina) discs and tubes were subject to vapor-phase exchange with gadolinium ions (Gd3+) using a gadolinium chloride salt (GdCl3) as a precursor to produce gadolinium beta double-prime alumina (Gd-β(doubleprime)-alumina) samples. Electrochemical impedance spectroscopy and microstructural analysis were performed on the ion-exchanged discs to determine the relationship between ion exchange and Gd3+ ion conductivity. The ion-exchanged tubes were configured as potentiometric sensors in order to monitor real-time Gd3+ ion concentrations in

  2. Roles of ion pairing on electroreduction of carbon dioxide based on imidazolium-based salts

    International Nuclear Information System (INIS)

    Highlights: • The significant electrocatalytic effects of imidazolium salts are due to a strong ion-pairing. • DFT calculation predicts the ion pair [BMIM+][CO2.−] conformation. • The extent of ion-pairing decreases with increasing the size of the alkyl substituent. - Abstract: The roles of ion pairing on CO2 electroreduction involving imidazolium-based salts are explored on an Ag electrode in a DMF solution. The electroreductive behaviours of CO2 and the IR results establish the dominant role of the cation of imidazolium-based salts in CO2 electrocatalytic reduction process. Density functional theory (DFT) calculations predict that the ion pair formation is mainly driven by the attraction of the four nearby and positively charged hydrogen atoms which are at the C2, N1 and N3-positions of an imidazolium cation for the negatively charged oxygen atoms in the CO2.− species. The electrostatic interaction between an imidazolium cation and the CO2.− species decreases with increasing the size of the alkyl substituent at the N1-position of that imidazolium cation

  3. Ion Dynamics Study of Potato Starch + Sodium Salts Electrolyte System

    Directory of Open Access Journals (Sweden)

    Tuhina Tiwari

    2013-01-01

    Full Text Available The effect of different anions, namely, SCN−, I−, and ClO4−, on the electrical properties of starch-based polymer electrolytes has been studied. Anion size and conductivity are having an inverse trend indicating systems to be predominantly anionic conductor. Impact of anion size and multiplet forming tendency is reflected in number of charge carriers and mobility, respectively. Ion dynamics study reveals the presence of different mechanisms in different frequency ranges. Interestingly, superlinear power law (SLPL is found to be present at <5 MHz frequency, which is further confirmed by dielectric data.

  4. Effect of Salt Stress on Transpiration and Ion Distribution in Seedlings of Four Tree Species

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Transpiration rate and ion distribution of pagoda tree, walnut, velvet ash and poplar seedlings treated by NaCl solution of 0, 50, 100, 200 mmol·L-1 were studied. The results showed that there were significant differences in the response to NaCl among the four tree species. Na+ exclusion capacity of pagoda tree was the largest among the four species. The Na+ exclusion capacity of velvet ash was less than that of pagoda tree. Salt excretion capacity of velvet ash was limited. Its salt-tolerance was bigge...

  5. LiGa(OTf)(sub 4) as an Electrolyte Salt for Li-Ion Cells

    Science.gov (United States)

    Reddy, V. Prakash; Prakash, G. K. Syria; Hu, Jinbo; Yan, Ping; Smart, Marshall; Bugga, ratnakumar; Chin, Keith; Surampudi, Subarao

    2008-01-01

    Lithium tetrakis(trifluoromethane sulfo - nato)gallate [abbreviated "LiGa(OTf)4" (wherein "OTf" signifies trifluoro - methanesulfonate)] has been found to be promising as an electrolyte salt for incorporation into both liquid and polymer electrolytes in both rechargeable and non-rechargeable lithium-ion electrochemical cells. This and other ingredients have been investigated in continuing research oriented toward im proving the performances of rechargeable lithium-ion electrochemical cells, especially at low temperatures. This research at earlier stages, and the underlying physical and chemical principles, were reported in numerous previous NASA Tech Briefs articles. As described in more detail in those articles, lithiumion cells most commonly contain nonaqueous electrolyte solutions consisting of lithium hexafluorophosphate (LiPF6) dissolved in mixtures of cyclic and linear alkyl carbonates, including ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), and ethyl methyl carbonate (EMC). Although such LiPF6-based electrolyte solutions are generally highly ionically conductive and electrochemically stable, as needed for good cell performance, there is interest in identifying alternate lithium electrolyte salts that, relative to LiPF6, are more resilient at high temperature and are less expensive. Experiments have been performed on LiGa(OTf)4 as well as on several other candidate lithium salts in pursuit of this interest. As part of these experiments, LiGa(OTf)4 was synthesized by the reaction of Ga(OTf)3 with an equimolar portion of LiOTf in a solvent consisting of anhydrous acetonitrile. Evaporation of the solvent yielded LiGa(OTf)4 as a colorless crystalline solid. The LiGa(OTf)4 and the other salts were incorporated into solutions with PC and DMC. The resulting electrolyte solutions exhibited reasonably high ionic conductivities over a relatively wide temperature range down to 40 C (see figure). In cyclic

  6. Effects of ion uptake for salt tolerance in several Mediterranean halophytes

    OpenAIRE

    Parra Boronat, Lorena; Llinares Palacios, Josep Vicent; Boscaiu Neagu, Mónica Tereza; Donat-Torres, M.P.; Vicente Meana, Óscar; Boira Tortajada, Herminio

    2013-01-01

    The patterns of ion uptake were analysed in three dicotyledonous (Arthrocnemum macrostachyum, Sarcocornia fruticosa and Inula crithmoides) and two monocotyledonous (Juncus acutus and J. maritimus) halophytes, collected from a salt marsh in SE Spain. The experimental design included four plots in different positions within the marsh, and three sampling periods corresponding to spring, summer and autumn 2011. Electric conductivity, pH, and Na+, K+, Ca2+, Mg2+ and Cl- contents were determined in...

  7. Comparative Salt Stress Study on Intracellular Ion Concentration in Marine and Salt-adapted Freshwater Strains of Microalgae

    Directory of Open Access Journals (Sweden)

    Ahmad Farhad TALEBI

    2013-08-01

    Full Text Available Salinity imposes significant stresses in various living organisms including microalgae. High extracellular concentration of Na+ directly influences ionic balance inside the cell and subsequently the cellular activities. In the present study, the effect of such stress on growth and intracellular ions concentration (IIC of Dunaliella salina and Chlorella Spp. was investigated. IIC was analyzed using Ion chromatography technique. D. salina showed the highest degree of resistance to increase in salinity as little changes occurred both in IIC and in growth parameters. D. salina could maintain the balance of K+ inside the cell and eject the excess Na+ even at NaCl concentrations above 1M. Moreover, D. salina accumulated β-carotene in order to protect its photosynthetic apparatus. Among Chlorella species, C. vulgaris showed signs of adaptation to high content of salinity, though it is a fresh water species by nature. Moreover, the response shown by C. vulgaris to rise in salinity was even stronger than that of C. salina, which is presumably a salt-water resistant species. In fact, C. vulgaris could maintain intracellular K+ better than C. salina in response to increasing salinity, and as a result, it could survive at NaCl concentrations as high as 0.75 M. Marine strains such as D. salina well cope with the fluctuations in salinity through the existing adaptation mechanisms i.e. maintaining the K+/N+ balance inside the cell, K+ accumulation and Na+ ejection, accumulation of photosynthetic pigments like β-carotene.

  8. Potassium salts of fatty acids as precipitating agents of alkaline earth metal ions

    International Nuclear Information System (INIS)

    Regularities have been studied of precipitation of ions of alkaline-earth elements with caprilate, pelargonate, caprinate, undecanate, laurate, tridecanate, myristate, pentadecanate, palmitate, and stearate of potassium. It has been shown that completeness of precipitation of metal ions is determined by the nature of alkaline-earth metal and potassium salt as well as by pH value and temperature of the solution. The study of temperature dependence of soaps of alkaline-earth metals makes it possible to calculate the heats of dissolution of laurates of alkaline-earth metals, and a change in entropy and free energy

  9. Scaling of cross-sections for asymmetric (, 3) process on helium-like ions by fast electrons

    Indian Academy of Sciences (India)

    M K Srivastava

    2004-11-01

    An approximate simple scaling law is obtained for asymmetric (, 3) process on helium-like ions for double ionization by fast electrons. It is based on the equation $(Z'^{3} /)$ exp$[−Z' (r_{1} + r_{2})]$, $Z' = Z − (5/16)$ for ground state wave function of helium- like ions and $Z'^{2}$ scaling of energies. The scaling law is found to work very well if the lower energy electron is ejected along the momentum transfer direction and the other one is ejected in the opposite direction. It also works quite well if this electron is ejected within about 90° of the momentum transfer direction with the other electron going in the opposite direction. The scaling law becomes increasingly accurate as the target nuclear charge and the energy increase.

  10. Ion motion in salt water flowing under a transverse magnetic field

    Directory of Open Access Journals (Sweden)

    De Luca R.

    2012-10-01

    Full Text Available The problem of ion motion in an electrolyte solution flowing in a thin rectangular duct with velocity VE in the presence of a transverse magnetic field B0 is studied by means of classical mechanics and electrodynamics. Because of Lorentz force on the ions in the electrolyte solution, a so called Faraday voltage appears at the electrodes orthogonal to both the field B0 and the velocity VE. The dynamics of positive and negative ions (cations and anions, respectively in this classical system is studied by taking into account the viscosity of the fluid and the process of charge accumulation on the opposite walls of the duct. Hydrogen production is seen to take place at one of the electrodes when salt water is taken as the flowing electrolyte.

  11. Reverse osmosis separation of some metal ions from mining effluents using heterogeneous asymmetric membranes

    International Nuclear Information System (INIS)

    Heterogeneous asymmetric membranes made from a blend of cellulose acetate and powdered coal were studied. The membranes were characterized in terms of pure water permeability constant A, solute transport parameter DAM/Kδ and mass transfer coefficient k of sodium chloride solution as the reference system. These membranes were used for treatment of mining and industrial effluents. Good separation and very high productivity were obtained at low operating pressure. (author). 3 refs, 3 tabs

  12. Lithium salt of tetrahydroxybenzoquinone: toward the development of a sustainable Li-ion battery.

    Science.gov (United States)

    Chen, Haiyan; Armand, Michel; Courty, Matthieu; Jiang, Meng; Grey, Clare P; Dolhem, Franck; Tarascon, Jean-Marie; Poizot, Philippe

    2009-07-01

    The use of lithiated redox organic molecules containing electrochemically active C=O functionalities, such as lithiated oxocarbon salts, is proposed. These represent alternative electrode materials to those used in current Li-ion battery technology that can be synthesized from renewable starting materials. The key material is the tetralithium salt of tetrahydroxybenzoquinone (Li(4)C(6)O(6)), which can be both reduced to Li(2)C(6)O(6) and oxidized to Li(6)C(6)O(6). In addition to being directly synthesized from tetrahydroxybenzoquinone by neutralization at room temperature, we demonstrate that this salt can readily be formed by the thermal disproportionation of Li(2)C(6)O(6) (dilithium rhodizonate phase) under an inert atmosphere. The Li(4)C(6)O(6) compound shows good electrochemical performance vs Li with a sustained reversibility of approximately 200 mAh g(-1) at an average potential of 1.8 V, allowing a Li-ion battery that cycles between Li(2)C(6)O(6) and Li(6)C(6)O(6) to be constructed. PMID:19476355

  13. Changes in transcript related to osmosis and intracellular ion homeostasis in Paulownia tomentosa under salt stress

    Directory of Open Access Journals (Sweden)

    Guoqiang eFan

    2016-03-01

    Full Text Available Paulownia tomentosa is an important economic and greening tree species that is cultivated widely, including salt environment. Our previous studies indicated its autotetraploid induced by colchicine showed better stress tolerance, but the underlying molecular mechanism related to ploidy and salt stress is still unclear. To investigate this issue, physiological measurements and transcriptome profiling of diploid and autotetraploid plants untreated and treated with NaCl were performed. Through the comparisons among four accessions, for one thing, we found different physiological changes between diploid and autotetraploid P. tomentosa; for another, and we detected many differentially expressed unigenes involved in salt stress response. These differentially expressed unigenes were assigned to several metabolic pathways, including plant hormone signal transduction, RNA transporter, protein processing in endoplasmic reticulum and plant-pathogen interaction, which constructed the complex regulatory network to maintain osmotic and intracellular ion homeostasis. Quantitative real-time polymerase chain reaction was used to confirm the expression patterns of 20 unigenes. The results establish the foundation for the genetic basis of salt tolerance in P. tomentosa, which in turn accelerates Paulownia breeding and expands available arable land.

  14. Changes in Transcript Related to Osmosis and Intracellular Ion Homeostasis in Paulownia tomentosa under Salt Stress.

    Science.gov (United States)

    Fan, Guoqiang; Wang, Limin; Deng, Minjie; Zhao, Zhenli; Dong, Yanpeng; Zhang, Xiaoshen; Li, Yongsheng

    2016-01-01

    Paulownia tomentosa is an important economic and greening tree species that is cultivated widely, including salt environment. Our previous studies indicated its autotetraploid induced by colchicine showed better stress tolerance, but the underlying molecular mechanism related to ploidy and salt stress is still unclear. To investigate this issue, physiological measurements and transcriptome profiling of diploid and autotetraploid plants untreated and treated with NaCl were performed. Through the comparisons among four accessions, for one thing, we found different physiological changes between diploid and autotetraploid P. tomentosa; for another, and we detected many differentially expressed unigenes involved in salt stress response. These differentially expressed unigenes were assigned to several metabolic pathways, including "plant hormone signal transduction," "RNA transporter," "protein processing in endoplasmic reticulum," and "plant-pathogen interaction," which constructed the complex regulatory network to maintain osmotic and intracellular ion homeostasis. Quantitative real-time polymerase chain reaction was used to confirm the expression patterns of 20 unigenes. The results establish the foundation for the genetic basis of salt tolerance in P. tomentosa, which in turn accelerates Paulownia breeding and expands available arable land. PMID:27066034

  15. Decreased Gap Width in a Cylindrical High-Field Asymmetric Waveform Ion Mobility Spectrometry Device Improves Protein Discovery.

    Science.gov (United States)

    Swearingen, Kristian E; Winget, Jason M; Hoopmann, Michael R; Kusebauch, Ulrike; Moritz, Robert L

    2015-12-15

    High-field asymmetric waveform ion mobility spectrometry (FAIMS) is an atmospheric pressure ion mobility technique that separates gas phase ions according to their characteristic dependence of ion mobility on electric field strength. FAIMS can be implemented as a means of automated gas-phase fractionation in liquid chromatography-tandem mass spectrometry (LC-MS/MS) experiments. We modified a commercially available cylindrical FAIMS device by enlarging the inner electrode, thereby narrowing the gap and increasing the effective field strength. This modification provided a nearly 4-fold increase in FAIMS peak capacity over the optimally configured unmodified device. We employed the modified FAIMS device for on-line fractionation in a proteomic analysis of a complex sample and observed major increases in protein discovery. NanoLC-FAIMS-MS/MS of an unfractionated yeast tryptic digest using the modified FAIMS device identified 53% more proteins than were identified using an unmodified FAIMS device and 98% more proteins than were identified with unaided nanoLC-MS/MS. We describe here the development of a nanoLC-FAIMS-MS/MS protocol that provides automated gas-phase fractionation for proteomic analysis of complex protein digests. We compare this protocol against prefractionation of peptides with isoelectric focusing and demonstrate that FAIMS fractionation yields comparable protein recovery while significantly reducing the amount of sample required and eliminating the need for additional sample handling. PMID:26560994

  16. Enhancement of mass spectrometry performance for proteomic analyses using high-field asymmetric waveform ion mobility spectrometry (FAIMS).

    Science.gov (United States)

    Bonneil, Eric; Pfammatter, Sibylle; Thibault, Pierre

    2015-11-01

    Remarkable advances in mass spectrometry sensitivity and resolution have been accomplished over the past two decades to enhance the depth and coverage of proteome analyses. As these technological developments expanded the detection capability of mass spectrometers, they also revealed an increasing complexity of low abundance peptides, solvent clusters and sample contaminants that can confound protein identification. Separation techniques that are complementary and can be used in combination with liquid chromatography are often sought to improve mass spectrometry sensitivity for proteomics applications. In this context, high-field asymmetric waveform ion mobility spectrometry (FAIMS), a form of ion mobility that exploits ion separation at low and high electric fields, has shown significant advantages by focusing and separating multiply charged peptide ions from singly charged interferences. This paper examines the analytical benefits of FAIMS in proteomics to separate co-eluting peptide isomers and to enhance peptide detection and quantitative measurements of protein digests via native peptides (label-free) or isotopically labeled peptides from metabolic labeling or chemical tagging experiments. PMID:26505763

  17. Effect of Surface and Salt Properties on the Ion Distribution around Spherical Nanoparticles: Monte Carlo Simulations.

    Science.gov (United States)

    Clavier, Arnaud; Carnal, Fabrice; Stoll, Serge

    2016-08-18

    Nanoparticle surface charge properties represent key parameters to predict their fate, reactivity, and complexation in natural, biological, and industrial dispersions. In this context, we present here an original approach to better understand the surface charge electrostatic properties of spherical nanoparticles (NPs). The ion distribution around one nanoparticle is investigated using Monte Carlo simulations and by adjusting a wide range of parameters including NP properties (surface charge density and site distribution), salt concentration (ionic strength and cation concentration), and salt valency (mono-, di-, and trivalent salt). A canonical Metropolis Monte Carlo method is used to reach equilibrium states and a primitive Coulomb model is applied to describe the electrostatic interactions between explicit discrete sites, counterions, and salt particles. Our results show that the presence of explicit surface charges on the NP and in solution has a strong influence on the local ion distribution and on the effective surface charge of the nanoparticles. The increase of surface charge density reduces the NP effective charge by the formation of a condensation layer around the nanoparticle. However, a limit of condensation is achieved due to steric effects and electrostatic repulsions. The presence of di- and trivalent cations is also found to strongly modify the effective charge and improve condensation state as long as electrostatic repulsion between the cations close to the surface are not so strong. At high trivalent cation concentration, the NP effective charge is greatly reduced and the local environment around the nanoparticle becomes more structured with the formation of a multi layer structure composed by anions and cations. PMID:27459187

  18. When do water-insoluble polyion-surfactant ion complex salts "redissolve" by added excess surfactant?

    Science.gov (United States)

    dos Santos, Salomé; Gustavsson, Charlotte; Gudmundsson, Christian; Linse, Per; Piculell, Lennart

    2011-01-18

    The redissolution of water-insoluble polyion-surfactant ion complexes by added excess of surfactant has systematically been investigated in experimental and theoretical phase equilibrium studies. A number of stoichiometric polyion-surfactant ion "complex salts" were synthesized and they consisted of akyltrimethylammonium surfactant ions of two different alkyl chain lengths (C(12)TA(+) and C(16)TA(+)) combined with homopolyions of polyacrylate of two different lengths (PA(-)(25) and PA(-)(6000)) or copolyions of acrylate and the slightly hydrophobic nonionic comonomers N-isopropylacrylamide (PA(-)-co-NIPAM) or N,N-dimethylacrylamide (PA(-)-co-DAM). The complex salts were mixed with water and excess alkyltrimethylammonium surfactant with either bromide or acetate counterions (C(n)TABr or C(n)TAAc). Factors promoting efficient redissolution were (i) very short polyions, (ii) a large fraction of NIPAM or DAM comonomers, and (iii) acetate, rather than bromide, as the surfactant counterion. Added C(12)TAAc gave an efficient redissolution of C(12)TAPA(25) but virtually no redissolution of C(12)TAPA(6000). A very efficient redissolution by added C(12)TAAc was obtained for PA(-)-co-NIPAM with 82 mol % of NIPAM. The C(12)TAPA-co-NIPAM/C(12)TAAc/H(2)O ternary phase diagram closely resembled the corresponding diagram for the much-studied pair cationic hydroxyethyl cellulose-(sodium) dodecyl sulfate. The simple Flory-Huggins theory adopted for polyelectrolyte systems successfully reproduced the main features of the experimental phase diagrams for the homopolyion systems, including the effect of the surfactant counterion. The efficient redissolution found for certain copolyion systems was explained by the formation of soluble polyion-surfactant ion complexes carrying an excess of surfactant ions through an additional hydrophobic attraction. PMID:21166446

  19. Effect of bisquaternary ammonium salts on complexing of metal ions with pyrocatechol violet

    International Nuclear Information System (INIS)

    Conditions for the improvement of contrast and sensitivity of reactions of high-charge ions of metals (Mo, W, La, Cd, Zr, Hf, Th) in the process of their photometric determination with pyrocatechol violet (PV), using bisquaternary ammonium salts (BQAS), have been studied. It is shown that in the systems investigated the BQAS play the role of ''shifting'' reagents, shifting bathochromically the absorption bands of different ligand complexes as compared with absorption bands of the Me-PV binary complexes. The effect of the BQAS on complexing with PV in aqueous and organic phases (chloroform) is studied and potential flotation of the compounds in the phase interface is considered

  20. Infrared spectroscopy of aqueous ionic salt mixtures at low concentrations: ion pairing in water.

    Science.gov (United States)

    Max, Jean-Joseph; Chapados, Camille

    2007-09-21

    The analysis by infrared spectroscopy of aqueous mixtures of NaI and CsCl was made in order to obtain information at the molecular level of the mixing of these two salts taken as model systems of strong electrolytes in water. In previous papers [J.-J. Max and C. Chapados, J. Chem. Phys. 115, 2664 (2001) and J.-J. Max et al., ibid. 126, 184507 (2007)] it was reported that a pure salt in water forms pairs of monoions to which are attached a fixed number of water molecules, giving solvated water species. Due to their interaction with the ion pairs, the solvated water molecules are strongly perturbed, modifying the IR water spectrum being monitored. After taking the IR spectrum of pure water, a small volume of NaI 2M was added and the IR spectrum taken. Then a small volume of CsCl 2M was added and a new IR spectrum taken. This procedure was repeated to obtain a series of 38 spectra in the 0.05M-0.83M concentration range. Factor analysis made on the series revealed the presence of three types of water: pure water and two salt solvated waters. The number of solvated water molecules on the two salts taken together is ten. Since NaI and CsCl have, respectively, 3.5 and 3.0 solvated water molecules, it was concluded that a reaction occurred in the solutions forming NaCl and CsI that have, respectively, five water molecules each for a total of ten. The analysis of the spectra of the orthogonal factors supports this attribution. These results provide additional proof of ion pairing in water. Furthermore, comparing the band displacements and intensity variations observed on the solvated water species to that of pure water indicates that the dielectric milieu surrounding the ion pairs is not constant. These results do not support the classical view of Debye-Huckel that considers that the ions are independent and the dielectric milieu constant. The present results give some in situ information on the reaction that goes on in "simple" electrolyte systems whose reactivity and

  1. Analysis of Supramolecular Complexes of 3-Methylxanthine with Field Asymmetric Waveform Ion Mobility Spectrometry Combined with Mass Spectrometry

    Science.gov (United States)

    Arthur, Kayleigh L.; Eiceman, Gary A.; Reynolds, James C.; Creaser, Colin S.

    2016-05-01

    Miniaturised field asymmetric waveform ion mobility spectrometry (FAIMS), combined with mass spectrometry (MS), has been applied to the study of self-assembling, noncovalent supramolecular complexes of 3-methylxanthine (3-MX) in the gas phase. 3-MX forms stable tetrameric complexes around an alkali metal (Na+, K+) or ammonium cation, to generate a diverse array of complexes with single and multiple charge states. Complexes of (3-MX)n observed include: singly charged complexes where n = 1-8 and 12 and doubly charged complexes where n = 12-24. The most intense ions are those associated with multiples of tetrameric units, where n = 4, 8, 12, 16, 20, 24. The effect of dispersion field on the ion intensities of the self-assembled complexes indicates some fragmentation of higher order complexes within the FAIMS electrodes (in-FAIMS dissociation), as well as in-source collision induced dissociation within the mass spectrometer. FAIMS-MS enables charge state separation of supramolecular complexes of 3-MX and is shown to be capable of separating species with overlapping mass-to-charge ratios. FAIMS selected transmission also results in an improvement in signal-to-noise ratio for low intensity complexes and enables the visualization of species undetectable without FAIMS.

  2. Interaction of the model alkyltrimethylammonium ions with alkali halide salts: an explicit water molecular dynamics study

    Directory of Open Access Journals (Sweden)

    M. Druchok

    2013-01-01

    Full Text Available We present an explicit water molecular dynamics simulation of dilute solutions of model alkyltrimethylammonium surfactant ions (number of methylene groups in the tail is 3, 5, 8, 10, and 12 in mixture with NaF, NaCl, NaBr, and NaI salts, respectively. The SPC/E model is used to describe water molecules. Results of the simulation at 298 K are presented in form of the radial distribution functions between nitrogen and carbon atoms of CH2 groups on the alkyltrimethylammonium ion, and the counterion species in the solution. The running coordination numbers between carbon atoms of surfactants and counterions are also calculated. We show that I- counterion exhibits the highest, and F- the lowest affinity to "bind" to the model surfactants. The results are discussed in view of the available experimental and simulation data for this and similar solutions.

  3. Induction of salt tolerance in Azolla microphylla Kaulf through modulation of antioxidant enzymes and ion transport.

    Science.gov (United States)

    Abraham, Gerard; Dhar, Dolly Wattal

    2010-09-01

    Azolla microphylla plants exposed directly to NaCl (13 dsm(-1)) did not survive the salinity treatment beyond a period of one day, whereas plants exposed directly to 4 and 9 dsm(-1) NaCl were able to grow and produce biomass. However, plants pre-exposed to NaCl (2 dsm(-1)) for 7 days on subsequent exposure to 13 dsm(-1) NaCl were able to grow and produce biomass although at a slow rate and are hereinafter designated as pre-exposed plants. The pre-exposed and directly exposed plants distinctly differed in their response to salt in terms of lipid peroxidation, proline accumulation, activity of antioxidant enzymes, such as SOD, APX, and CAT, and Na(+)/K(+) ratio. Efficient modulation of antioxidant enzymes coupled with regulation of ion transport play an important role in the induction of salt tolerance. Results show that it is possible to induce salt adaptation in A. microphylla by pre-exposing them to low concentrations of NaCl. PMID:20422236

  4. Sorption of rare earth ions by alkylammonium salts of transition metal polyacids

    International Nuclear Information System (INIS)

    Consideration is given to results of investigations into gadolinium extraction from aqueous solutions by coprecipitation with hydrophobic compounds, formed during direct interaction of 12-tungstophosphoric acid (HPA) with surfactants (SA), depending on aqueous phase acidity, as well as SA nature and content. It was established that degree of gadolinium extraction increased with growth of pH value of the medium: gadolinium is concentrated in strong-acid media, as compared to yttrium. The process of gadolinium coprecipitation with HPA salts is also affected by the nature of precipitant: degree of metal extraction growth with increase of SA molecular mass. Gadolinium interaction with HPA salts takes place in result of ion exchange with salt-forming HPA protons. Data of IR spectroscopic investigations of the composition of hydrophobic precipitates, prepared under different conditions, are presented. Their content is not changed at different initial concentrations of HPA and gadolinium and depends only on pH of aqueous medium. Data of potentiometric titration of the compounds, supporting differences in interaction of gadolinium and yttrium with HPA, are presented

  5. Pre-equilibrium dipole strength in charge asymmetric peripheral heavy-ion reactions

    International Nuclear Information System (INIS)

    We report on the results obtained from the study of the 32S+64Ni and 32S+58Ni peripheral reactions at incident energies Elab=288 MeV and Elab=320 MeV, respectively. High-energy γ-rays were detected in an array of 8 seven-pack BaF2 clusters. Coincidence with complex fragments detected in 12 three-stage telescopes ensured the selection of peripheral reaction events. All of the relevant reaction parameters were kept constant with the exception of the different initial dipole moment caused by the different entrance channel charge asymmetry. While for quasi-elastic events no N/Z effect was observed in the differential γ-ray multiplicities of the two reactions, for deep-inelastic events a larger dipole γ-ray emission occurs during the more N/Z asymmetric reaction. A theoretical interpretation based on a collective Bremsstrahlung analysis of the reaction dynamics is presented. (orig.)

  6. Influence of symmetry energy on the multifragmentation of asymmetric heavy-ion collisions

    International Nuclear Information System (INIS)

    In order to study the role of different density dependencies of symmetry energy on fragmentation pattern, we simulated thousands of events for the asymmetric collisions of 40Ar + 64Cu,108Ag, 197Au using soft equation of state supplemented by energy-dependent nucleon-nucleon cross-section reduced by 20%, i.e, σnn = 0.8 σfreenn free for three different values of γ= 0.5, 1 and 2. The choice of colliding geometry and incident energies is guided from the experimental measurements. As these reactions cover wide range of asymmetry (η = 0.2-0.6) and experimental measurements are also available, so we simulate these reactions to study the effect of different density dependencies of symmetry energy

  7. Charged patchy particle models in explicit salt: Ion distributions, electrostatic potentials, and effective interactions

    International Nuclear Information System (INIS)

    We introduce a set of charged patchy particle models (CPPMs) in order to systematically study the influence of electrostatic charge patchiness and multipolarity on macromolecular interactions by means of implicit-solvent, explicit-ion Langevin dynamics simulations employing the Gromacs software. We consider well-defined zero-, one-, and two-patched spherical globules each of the same net charge and (nanometer) size which are composed of discrete atoms. The studied mono- and multipole moments of the CPPMs are comparable to those of globular proteins with similar size. We first characterize ion distributions and electrostatic potentials around a single CPPM. Although angle-resolved radial distribution functions reveal the expected local accumulation and depletion of counter- and co-ions around the patches, respectively, the orientation-averaged electrostatic potential shows only a small variation among the various CPPMs due to space charge cancellations. Furthermore, we study the orientation-averaged potential of mean force (PMF), the number of accumulated ions on the patches, as well as the CPPM orientations along the center-to-center distance of a pair of CPPMs. We compare the PMFs to the classical Derjaguin-Verwey-Landau-Overbeek theory and previously introduced orientation-averaged Debye-Hückel pair potentials including dipolar interactions. Our simulations confirm the adequacy of the theories in their respective regimes of validity, while low salt concentrations and large multipolar interactions remain a challenge for tractable theoretical descriptions

  8. Charged patchy particle models in explicit salt: Ion distributions, electrostatic potentials, and effective interactions

    Energy Technology Data Exchange (ETDEWEB)

    Yigit, Cemil; Dzubiella, Joachim, E-mail: joachim.dzubiella@helmholtz-berlin.de [Soft Matter and Functional Materials, Helmholtz-Zentrum Berlin, 14109 Berlin (Germany); Helmholtz Virtual Institute “Multifunctional Biomaterials for Medicine,” 14513 Teltow (Germany); Institut für Physik, Humboldt-Universität zu Berlin, 12489 Berlin (Germany); Heyda, Jan [Department of Physical Chemistry, University of Chemistry and Technology, Prague, 166 28 Praha 6 (Czech Republic)

    2015-08-14

    We introduce a set of charged patchy particle models (CPPMs) in order to systematically study the influence of electrostatic charge patchiness and multipolarity on macromolecular interactions by means of implicit-solvent, explicit-ion Langevin dynamics simulations employing the Gromacs software. We consider well-defined zero-, one-, and two-patched spherical globules each of the same net charge and (nanometer) size which are composed of discrete atoms. The studied mono- and multipole moments of the CPPMs are comparable to those of globular proteins with similar size. We first characterize ion distributions and electrostatic potentials around a single CPPM. Although angle-resolved radial distribution functions reveal the expected local accumulation and depletion of counter- and co-ions around the patches, respectively, the orientation-averaged electrostatic potential shows only a small variation among the various CPPMs due to space charge cancellations. Furthermore, we study the orientation-averaged potential of mean force (PMF), the number of accumulated ions on the patches, as well as the CPPM orientations along the center-to-center distance of a pair of CPPMs. We compare the PMFs to the classical Derjaguin-Verwey-Landau-Overbeek theory and previously introduced orientation-averaged Debye-Hückel pair potentials including dipolar interactions. Our simulations confirm the adequacy of the theories in their respective regimes of validity, while low salt concentrations and large multipolar interactions remain a challenge for tractable theoretical descriptions.

  9. Influence of silicon on microdistribution of mineral ions in roots of salt-stressed barley as associated with salt tolerance in plants

    Institute of Scientific and Technical Information of China (English)

    梁永超; 丁瑞兴

    2002-01-01

    Two contrasting barley (Hordeum vulgare L.) cultivars: Kepin No.7 (salt sensitive), and Jian 4 (salt tolerant) were grown hydroponically to investigate the microdistribution of mineral ions in roots as affected by silicon (Si) with respect to salt tolerance. The experiment was undertaken consisting of two treatments with 3 replicates: (i) 120 mmol@L?1 NaCl alone (referred to as Si(NaCl+), (ii) 120 mmol@L?1 NaCl + 1.0 mmol@L?1 Si (as potassium silicate) (referred to as Si+NaCl+). Plant root tips were harvested for microanalysis using an energy dispersive X-ray microanalyzer (EDX) 30 d after transplanting. Higher Cl and Na X-ray peaks were recorded in the root epidermal, cortical and stelar cells of roots for the treatment Si(NaCl+ with the majorities of Na and Cl being accumulated in epidermal and cortical cells, while relatively low K peaks were observed regardless of the barley cultivars used. By contrast, considerably higher K peaks were detected in the epidermal, cortical and stelar cells of the roots for the treatment Si+NaCl+, but lower Cl and Na peaks were also observed for this treatment with both Na and Cl ions being evenly distributed in the epidermal, cortical and stelar cells. These findings directly support our previous finding, which showed that Si depressed the uptake of sodium but enhanced the uptake of potassium by salt-stressed barley. We believe that one of the possible mechanisms involved in Si-enhancement of salt tolerance in barley is attributed to the Si-induced changes in the uptake and microdistribution of mineral ions in plants.

  10. Asymmetrical response of dayside ion precipitation to a large rotation of the IMF

    Science.gov (United States)

    Berchem, J.; Richard, R. L.; Escoubet, C. P.; Wing, S.; Pitout, F.

    2016-01-01

    We have carried out global magnetohydrodynamics (MHD) simulations together with large-scale kinetic simulations to investigate the response of the dayside magnetospheric ion precipitation to a large rotation (135°) of the interplanetary magnetic field (IMF). The study uses simplified global MHD model (no dipole tilt and constant ionospheric conductance) and idealized solar wind conditions where the IMF rotates smoothly from a southward toward a northward direction (BX = 0) to clearly identify the effects of the impact of the discontinuity on the magnetopause. Results of the global simulations reveal that a strong north-south asymmetry develops in the pattern of precipitating ions during the interaction of the IMF rotation with the magnetopause. For a counterclockwise IMF rotation from its original southward direction (BY original southward direction (BY > 0). Trends observed in the ion dispersions predicted from the simulations are in good agreement with Cluster observations of the midaltitude northern cusp, which motivated the study.

  11. RF reactor with asymmetrical electrodes for reactive ion etching of semiconductors

    Directory of Open Access Journals (Sweden)

    Dudin S. V.

    2011-04-01

    Full Text Available Results of experimental and theoretical study of RF CCP reactor for reactive ion etching of semiconductors are presented. Breakdown curve and domain of the discharge existence are measured in various gases (argon, fluorocarbon, oxygen. The dependences of the DC selfbias potential on the RF voltage applied to the electrode have been found. The radial profiles of the ion current density to the processed surface and their behavior with the discharge parameters change are presented for various gases. The experimental data are compared to the numerical simulation results obtained using the OOPIC code.

  12. Nontarget analysis of urine by electrospray ionization-high field asymmetric waveform ion mobility-tandem mass spectrometry.

    Science.gov (United States)

    Beach, Daniel G; Gabryelski, Wojciech

    2011-12-01

    Nearly a decade after first commercialization, high field asymmetric waveform ion mobility spectrometry (FAIMS) has yet to find its place in routine chemical analysis. Prototypes have been used to demonstrate the utility of this separation technique combined with mass spectrometry (MS). Unfortunately, first generation commercial FAIMS instruments have gone practically unused by early adopters. Here, we show this to be due to poor ion transmission in the FAIMS-MS source interface. We present simple instrumental modifications and optimization of experimental conditions to achieve good performance from the first generation commercial FAIMS device (the Ionalytics Selectra) coupled to a high resolution Q-TOF-MS. In combination with nanospray ionization, we demonstrate for the first time the nontarget analysis of urine by FAIMS with minimal sample preparation. We show the unique suitability of electrospray ionization (ESI)-FAIMS-MS for identification of low abundance species such as urinary biomarkers of damage of nucleic acids in a complex biological matrix. The elimination of electrospray noise and matrix components by FAIMS and the continuous flow of analytes through FAIMS for accurate and tandem mass analysis produce high quality spectral data suitable for structural identification of unknowns. These characteristics make ESI-FAIMS-MS ideal for nontarget identification, even when compared to high efficiency LC-ESI-MS. PMID:21978137

  13. A 2D ion chamber array audit of wedged and asymmetric fields in an inhomogeneous lung phantom

    International Nuclear Information System (INIS)

    Purpose: The Australian Clinical Dosimetry Service (ACDS) has implemented a new method of a nonreference condition Level II type dosimetric audit of radiotherapy services to increase measurement accuracy and patient safety within Australia. The aim of this work is to describe the methodology, tolerances, and outcomes from the new audit. Methods: The ACDS Level II audit measures the dose delivered in 2D planes using an ionization chamber based array positioned at multiple depths. Measurements are made in rectilinear homogeneous and inhomogeneous phantoms composed of slabs of solid water and lung. Computer generated computed tomography data sets of the rectilinear phantoms are supplied to the facility prior to audit for planning of a range of cases including reference fields, asymmetric fields, and wedged fields. The audit assesses 3D planning with 6 MV photons with a static (zero degree) gantry. Scoring is performed using local dose differences between the planned and measured dose within 80% of the field width. The overall audit result is determined by the maximum dose difference over all scoring points, cases, and planes. Pass (Optimal Level) is defined as maximum dose difference ≤3.3%, Pass (Action Level) is ≤5.0%, and Fail (Out of Tolerance) is >5.0%. Results: At close of 2013, the ACDS had performed 24 Level II audits. 63% of the audits passed, 33% failed, and the remaining audit was not assessable. Of the 15 audits that passed, 3 were at Pass (Action Level). The high fail rate is largely due to a systemic issue with modeling asymmetric 60° wedges which caused a delivered overdose of 5%–8%. Conclusions: The ACDS has implemented a nonreference condition Level II type audit, based on ion chamber 2D array measurements in an inhomogeneous slab phantom. The powerful diagnostic ability of this audit has allowed the ACDS to rigorously test the treatment planning systems implemented in Australian radiotherapy facilities. Recommendations from audits have led to

  14. Novel benzimidazole salts for lithium ion battery electrolytes: effects of substituents.

    Science.gov (United States)

    Sriana, T; Leggesse, E G; Jiang, J C

    2015-07-01

    In this paper, we report on our effort to design a novel lithium salt derived from bis(trifluoroborane)benzimidazolide by using density functional theory (DFT) calculations. The effects of different substituents are investigated with respect to ion pair dissociation energies and intrinsic anion oxidation potential of the molecules. Based on our calculations, we have found that ion pair dissociation energies and intrinsic anion oxidation potentials of the anions are mainly affected by the position and the type of substituents introduced into the parent structure. Compared to -CH3, substitution at the C2 position of the parent bis(trifluoroborane)benzimidazole (BTB(-)) by -CF3 results in an increase in anion oxidation stability. However, we observed a negligible change in the intrinsic anion oxidation potential as the length of the fluoroalkyl group increased to -C2F5. The most promising anions are generated by considering double-substitution at C2 and C5 positions. Among the possible anions, bis(trifluoroborane)-5-nitro-2-(trifluoromethyl) benzimidazolide (BTNTB(-)), with the calculated intrinsic anion oxidation potential of 5.50 V vs. Li(+)/Li, can be considered as a potential candidate for high voltage Li-ion batteries. PMID:26051990

  15. Measurements of ion temperature and flow velocity using symmetric and asymmetric double probes in the boundary plasma of the JFT-2M tokamak

    International Nuclear Information System (INIS)

    The radial profiles of the ion temperature as well as the flow velocity have been measured by using rotatable symmetric and asymmetric double probes in the boundary plasma of the JFT-2M tokamak. It has been found that the ion temperature is higher than the electron temperature by a factor of about 10, and the flow velocity is 0.2-0.3 of the ion sound velocity in the SOL for both ohmic and NB injection heating. These data can help to determine the cross-field thermal diffusivity in tokamak boundary plasma. (author)

  16. Collective flow and balance energy in asymmetric heavy-ion collisions

    International Nuclear Information System (INIS)

    Heavy-ion collisions at intermediate energy provide a useful tool to determine the nuclear matter equation of state as well as in-medium nucleon-nucleon (nn) cross-section. We therefore, aim to study the transverse in-plane flow as well as its disappearance for different colliding nuclei with varying asymmetry. We plan to address this question using quantum molecular dynamics (QMD) model

  17. Multifragmentation in asymmetric heavy-ion collisions. An experimental trace search

    International Nuclear Information System (INIS)

    The author presents a review about experimental studies of multifragmentation in heavy ion collisions. After a description of the experimental methods for the study of such processes he describes the emission characteristics of medium heavy fragments like energy and angular distribution, production cross sections, and multiplicity. Then he considers statistical aspects of highly excited nuclei. Then the production of unstable fragments is discussed. Finally the author discusses the study of pp correlations looking for interference effects. (HSI)

  18. Lithium recovery by means of electrochemical ion pumping: a comparison between salt capturing and selective exchange.

    Science.gov (United States)

    Trocoli, Rafael; Bidhendi, Ghoncheh Kasiri; La Mantia, Fabio

    2016-03-23

    Currently, lithium carbonate is mainly produced through evaporation of lithium-rich brines, which are located in South American countries such as Bolivia, Chile, and Argentina. The most commonly used process, the lime-soda evaporation, requires a long time and several purification steps, which produces a considerable amount of chemical waste. Recently, several alternative electrochemical methods, based on LiFePO4 as a selective lithium capturing electrode and differing for the reaction at the counter electrode, have been proposed. In this work a comparison between the salt capturing method, based on silver / silver chloride reaction, and the selective exchange method, based on ion intercalation reaction in a Prussian Blue derivative, is performed in terms of energy consumption. In particular, the energy consumption is divided in thermodynamic and kinetic contribution, and the theoretical calculations are compared with the experimental results. The experimental results show a good agreement with the theoretical calculation. The selective exchange method shows superior performances to the salt exchange in terms of purity and efficiency, however the energy consumption is higher. PMID:26910577

  19. Lithium recovery by means of electrochemical ion pumping: a comparison between salt capturing and selective exchange

    International Nuclear Information System (INIS)

    Currently, lithium carbonate is mainly produced through evaporation of lithium-rich brines, which are located in South American countries such as Bolivia, Chile, and Argentina. The most commonly used process, the lime–soda evaporation, requires a long time and several purification steps, which produces a considerable amount of chemical waste. Recently, several alternative electrochemical methods, based on LiFePO4 as a selective lithium capturing electrode and differing for the reaction at the counter electrode, have been proposed. In this work a comparison between the salt capturing method, based on silver / silver chloride reaction, and the selective exchange method, based on ion intercalation reaction in a Prussian Blue derivative, is performed in terms of energy consumption. In particular, the energy consumption is divided in thermodynamic and kinetic contribution, and the theoretical calculations are compared with the experimental results. The experimental results show a good agreement with the theoretical calculation. The selective exchange method shows superior performances to the salt exchange in terms of purity and efficiency, however the energy consumption is higher. (paper)

  20. Spatial Variability of Salt Ions in Soils in Oasis of Delta of Weigan River-Kuqa River in Different Seasons

    Institute of Scientific and Technical Information of China (English)

    Yuanyuan XU; Tashpolat TIYIP; Fei ZHANG; Jun XIA; Guihong HAN; Mamat SAWUT

    2012-01-01

    Abstract [Objective] The aim was to research the spatial variability of salts' ions in soils of oases of Weigan River-Kuqa River to explore spatial correlation among soil ions and effects of seasonal changes on distribution of eight ions in soils. [Method] Based on soil salinizaiton, temporal and spatial distributions of eight ions in surface soils were researched and distribution maps were drawn with the help of classical statistics and geostatistics. [Result] All contents of salt ions were proved in consistent with normal distribution by K-S test, and variability of the ions changed with season, for example, variability of ions in soils in October was higher than that in April, which might be caused by little rainfall and high evaporation in October. It can be concluded from semivariance analysis that salt ions were all of high spatial autocorrelation. In addition, it can be concluded from spatial distribution that spatial structures of most ions are reasonable, except Ca2+ and Mg2' in soils collected in April of 2010 and Mg2+ in October of 2010, which were more suitable for linear model, and chloride-sulfate dominated in salinized soils in the researching area. [Conclusion] The research laid foundation for partition, improvement and use of salin- ized soils in delta of Weigan River-Kuqa River.

  1. Primary amine/CSA ion pair: A powerful catalytic system for the asymmetric enamine catalysis

    KAUST Repository

    Liu, Chen

    2011-05-20

    A novel ion pair catalyst containing a chiral counteranion can be readily derived by simply mixing cinchona alkaloid-derived diamine with chiral camphorsulfonic acid (CSA). A mixture of 9-amino(9-deoxy)epi-quinine 8 and (-)-CSA was found to be the best catalyst with matching chirality, enabling the direct amination of α-branched aldehydes to proceed in quantitative yields and with nearly perfect enantioselectivities. A 0.5 mol % catalyst loading was sufficient to catalyze the reaction, and a gram scale enantioselective synthesis of biologically important α-methyl phenylglycine has been successfully demonstrated. © 2011 American Chemical Society.

  2. ZIF-8 Derived, Nitrogen-Doped Porous Electrodes of Carbon Polyhedron Particles for High-Performance Electrosorption of Salt Ions

    Science.gov (United States)

    Liu, Nei-Ling; Dutta, Saikat; Salunkhe, Rahul R.; Ahamad, Tansir; Alshehri, Saad M.; Yamauchi, Yusuke; Hou, Chia-Hung; Wu, Kevin C.-W.

    2016-01-01

    Three-dimensional (3-D) ZIF-8 derived carbon polyhedrons with high nitrogen (N) content, (denoted as NC-800) are synthesized for their application as high-performance electrodes in electrosorption of salt ions. The results showed a high specific capacitance of 160.8 F·g−1 in 1 M NaCl at a scan rate of 5 mV·s−1. Notably, integration of 3-D mesopores and micropores in NC-800 achieves an excellent capacitive deionization (CDI) performance. The electrosorption of salt ions at the electrical double layer is enhanced by N-doping at the edges of a hexagonal lattice of NC-800. As evidenced, when the initial NaCl solution concentration is 1 mM, the resultant NC-800 exhibits a remarkable CDI potential with a promising salt electrosorption capacity of 8.52 mg·g−1. PMID:27404086

  3. ZIF-8 Derived, Nitrogen-Doped Porous Electrodes of Carbon Polyhedron Particles for High-Performance Electrosorption of Salt Ions.

    Science.gov (United States)

    Liu, Nei-Ling; Dutta, Saikat; Salunkhe, Rahul R; Ahamad, Tansir; Alshehri, Saad M; Yamauchi, Yusuke; Hou, Chia-Hung; Wu, Kevin C-W

    2016-01-01

    Three-dimensional (3-D) ZIF-8 derived carbon polyhedrons with high nitrogen (N) content, (denoted as NC-800) are synthesized for their application as high-performance electrodes in electrosorption of salt ions. The results showed a high specific capacitance of 160.8 F·g(-1) in 1 M NaCl at a scan rate of 5 mV·s(-1). Notably, integration of 3-D mesopores and micropores in NC-800 achieves an excellent capacitive deionization (CDI) performance. The electrosorption of salt ions at the electrical double layer is enhanced by N-doping at the edges of a hexagonal lattice of NC-800. As evidenced, when the initial NaCl solution concentration is 1 mM, the resultant NC-800 exhibits a remarkable CDI potential with a promising salt electrosorption capacity of 8.52 mg·g(-1). PMID:27404086

  4. On-line method to study dynamics of ion adsorption from mixtures of salts in capacitive deionization

    NARCIS (Netherlands)

    Dykstra, J.E.; Dijkstra, J.; Wal, van der A.; Hamelers, H.V.M.; Porada, S.

    2016-01-01

    Capacitive Deionization (CDI) is a water desalination technology that adsorbs ions into two oppositely polarized porous carbon electrodes, under the action of an applied voltage. Here, we introduce a novel method to analyze the effluent concentration of multiple ionic species in mixtures of salt

  5. Synthesis and Self-Assembly of Triangulenium Salts

    DEFF Research Database (Denmark)

    Shi, Dong

    -processed self-assembling method was developed to make aggregates with uniform morphologies and excellent stabilities in an equilibrium state either with pure ATOTA+ salts or with mixed systems of ATOTA+ salts and lipid molecules in aqueous media. Special emphasis was given to effects of the counterions in......-assembly and triangulenium salts. Chapters 3 to 6 are mainly focused on the synthesis and self-assembly of trioxatriangulenium salts in aqueous media. In particular, chapter 3 reports a direct selfassembly of a synthetic triangulenium salt mixed with DMPC lipid (5/95 by molar ratio) to make mono disperse......This thesis describes the design and synthesis of asymmetrically substituted amphiphilic tis(dialkylamino)trioxiatriangulenium (ATOTA+) salts with different counter ions. Attention was focused on exploring the assembling properties of the ATOTA+ salts in aqueous media. A direct vortexing...

  6. Detection of potato storage disease via gas analysis: a pilot study using field asymmetric ion mobility spectrometry.

    Science.gov (United States)

    Rutolo, Massimo; Covington, James A; Clarkson, John; Iliescu, Daciana

    2014-01-01

    Soft rot is a commonly occurring potato tuber disease that each year causes substantial losses to the food industry. Here, we explore the possibility of early detection of the disease via gas/vapor analysis, in a laboratory environment, using a recent technology known as FAIMS (Field Asymmetric Ion Mobility Spectrometry). In this work, tubers were inoculated with a bacterium causing the infection, Pectobacterium carotovorum, and stored within set environmental conditions in order to manage disease progression. They were compared with controls stored in the same conditions. Three different inoculation time courses were employed in order to obtain diseased potatoes showing clear signs of advanced infection (for standard detection) and diseased potatoes with no apparent evidence of infection (for early detection). A total of 156 samples were processed by PCA (Principal Component Analysis) and k-means clustering. Results show a clear discrimination between controls and diseased potatoes for all experiments with no difference among observations from standard and early detection. Further analysis was carried out by means of a statistical model based on LDA (Linear Discriminant Analysis) that showed a high classification accuracy of 92.1% on the test set, obtained via a LOOCV (leave-one out cross-validation). PMID:25171118

  7. Detection of Potato Storage Disease via Gas Analysis: A Pilot Study Using Field Asymmetric Ion Mobility Spectrometry

    Directory of Open Access Journals (Sweden)

    Massimo Rutolo

    2014-08-01

    Full Text Available Soft rot is a commonly occurring potato tuber disease that each year causes substantial losses to the food industry. Here, we explore the possibility of early detection of the disease via gas/vapor analysis, in a laboratory environment, using a recent technology known as FAIMS (Field Asymmetric Ion Mobility Spectrometry. In this work, tubers were inoculated with a bacterium causing the infection, Pectobacterium carotovorum, and stored within set environmental conditions in order to manage disease progression. They were compared with controls stored in the same conditions. Three different inoculation time courses were employed in order to obtain diseased potatoes showing clear signs of advanced infection (for standard detection and diseased potatoes with no apparent evidence of infection (for early detection. A total of 156 samples were processed by PCA (Principal Component Analysis and k-means clustering. Results show a clear discrimination between controls and diseased potatoes for all experiments with no difference among observations from standard and early detection. Further analysis was carried out by means of a statistical model based on LDA (Linear Discriminant Analysis that showed a high classification accuracy of 92.1% on the test set, obtained via a LOOCV (leave-one out cross-validation.

  8. Elucidation of transport mechanism and enhanced alkali ion transference numbers in mixed alkali metal-organic ionic molten salts.

    Science.gov (United States)

    Chen, Fangfang; Forsyth, Maria

    2016-07-28

    Mixed salts of Ionic Liquids (ILs) and alkali metal salts, developed as electrolytes for lithium and sodium batteries, have shown a remarkable ability to facilitate high rate capability for lithium and sodium electrochemical cycling. It has been suggested that this may be due to a high alkali metal ion transference number at concentrations approaching 50 mol% Li(+) or Na(+), relative to lower concentrations. Computational investigations for two IL systems illustrate the formation of extended alkali-anion aggregates as the alkali metal ion concentration increases. This tends to favor the diffusion of alkali metal ions compared with other ionic species in electrolyte solutions; behavior that has recently been reported for Li(+) in a phosphonium ionic liquid, thus an increasing alkali transference number. The mechanism of alkali metal ion diffusion via this extended coordination environment present at high concentrations is explained and compared to the dynamics at lower concentrations. Heterogeneous alkali metal ion dynamics are also evident and, somewhat counter-intuitively, it appears that the faster ions are those that are generally found clustered with the anions. Furthermore these fast alkali metal ions appear to correlate with fastest ionic liquid solvent ions. PMID:27375042

  9. Membrane curvature generated by asymmetric depletion layers of ions, small molecules, and nanoparticles.

    Science.gov (United States)

    Różycki, Bartosz; Lipowsky, Reinhard

    2016-08-21

    Biomimetic and biological membranes consist of molecular bilayers with two leaflets that are typically exposed to different aqueous solutions. We consider solutions of "particles" that experience effectively repulsive interactions with these membranes and form depletion layers in front of the membrane leaflets. The particles considered here are water-soluble, have a size between a few angstrom and a few nanometers as well as a rigid, more or less globular shape, and do neither adsorb onto the membranes nor permeate these membranes. Examples are provided by ions, small sugar molecules, globular proteins, or inorganic nanoparticles with a hydrophilic surface. We first study depletion layers in a hard-core system based on ideal particle solutions as well as hard-wall interactions between these particles and the membrane. For this system, we obtain exact expressions for the coverages and tensions of the two leaflets as well as for the spontaneous curvature of the bilayer membrane. All of these quantities depend linearly on the particle concentrations. The exact results for the hard-core system also show that the spontaneous curvature can be directly deduced from the planar membrane geometry. Our results for the hard-core system apply both to ions and solutes that are small compared to the membrane thickness and to nanoparticles with a size that is comparable to the membrane thickness, provided the particle solutions are sufficiently dilute. We then corroborate the different relationships found for the hard-core system by extensive simulations of a soft-core particle system using dissipative particle dynamics. The simulations confirm the linear relationships obtained for the hard-core system. Both our analytical and our simulation results show that the spontaneous curvature induced by a single particle species can be quite large. When one leaflet of the membrane is exposed, e.g., to a 100 mM solution of glucose, a lipid bilayer can acquire a spontaneous curvature of ±1

  10. Effects of salt stress on ion balance and nitrogen metabolism of old and young leaves in rice (Oryza sativa L.

    Directory of Open Access Journals (Sweden)

    Wang Huan

    2012-10-01

    Full Text Available Abstract Background It is well known that salt stress has different effects on old and young tissues. However, it remains largely unexplored whether old and young tissues have different regulatory mechanism during adaptation of plants to salt stress. The aim of this study was to investigate whether salt stress has different effects on the ion balance and nitrogen metabolism in the old and young leaves of rice, and to compare functions of both organs in rice salt tolerance. Results Rice protected young leaves from ion harm via the large accumulation of Na+ and Cl− in old leaves. The up-regulation of OsHKT1;1, OsHAK10 and OsHAK16 might contribute to accumulation of Na+ in old leaves under salt stress. In addition, lower expression of OsHKT1;5 and OsSOS1 in old leaves may decrease frequency of retrieving Na+ from old leaf cells. Under salt stress, old leaves showed higher concentration of NO3− content than young leaves. Up-regulation of OsNRT1;2, a gene coding nitrate transporter, might contribute to the accumulation of NO3− in the old leaves of salt stressed-rice. Salt stress clearly up-regulated the expression of OsGDH2 and OsGDH3 in old leaves, while strongly down-regulated expression of OsGS2 and OsFd-GOGAT in old leaves. Conclusions The down-regulation of OsGS2 and OsFd-GOGAT in old leaves might be a harmful response to excesses of Na+ and Cl−. Under salt stress, rice might accumulate Na+ and Cl− to toxic levels in old leaves. This might influence photorespiration process, reduce NH4+ production from photorespiration, and immediately down-regulate the expression of OsGS2 and OsFd-GOGAT in old leaves of salt stressed rice. Excesses of Na+ and Cl− also might change the pathway of NH4+ assimilation in old leaves of salt stressed rice plants, weaken GOGAT/GS pathway and elevate GDH pathway.

  11. Li+ Ion Transport in Polymer Electrolytes Based on a Glyme-Li Salt Solvate Ionic Liquid

    International Nuclear Information System (INIS)

    Polymer electrolytes (PEs) have served as the focus of intensive research as new ion-conducting materials, especially for lithium battery applications. A new strategy to develop fast lithium-conducting PEs is reported here. The thermal, ionic transport, and electrochemical properties of polymer solutions in a glyme-Li salt solvate ionic liquid, [Li(G4)1][TFSA], composed of an equimolar mixture of lithium bis(trifluoromethanesulfonyl) amide (Li[TFSA]) and tetraglyme (G4), were characterized. Poly(ethylene oxide) (PEO), poly(methyl methacrylate) (PMMA), and poly(butyl acrylate) (PBA) were combined with [Li(G4)1][TFSA] in order to explore the effects of polymer structure on the properties. The self-diffusion coefficient ratio of the glyme and Li+ ions (DG/DLi) was investigated to evaluate the stability of the complex (solvate) cations. The DG/DLi values suggested that the [Li(G4)1]+ complex cations underwent a ligand exchange reaction between G4 and PEO in the PEO-based solution, whereas the cations remained stable (DG/DLi = 1) in the PMMA- and PBA-based solutions. The robustness of the [Li(G4)1]+ complex cations in the PMMA- and PBA-based solutions was reflected in high weight-loss temperature, greater Li transference number, and high oxidative stability. Owing to the lower glass transition temperature and low affinity towards Li+ ions, the PBA-based solutions yielded superior lithium transport properties (ionic conductivity of 10−4∼10−3 Scm−1 and Li transference number as high as 0.5) among the investigated polymer solutions

  12. LITERATURE REVIEWS TO SUPPORT ION EXCHANGE TECHNOLOGY SELECTION FOR MODULAR SALT PROCESSING

    Energy Technology Data Exchange (ETDEWEB)

    King, W

    2007-11-30

    This report summarizes the results of literature reviews conducted to support the selection of a cesium removal technology for application in a small column ion exchange (SCIX) unit supported within a high level waste tank. SCIX is being considered as a technology for the treatment of radioactive salt solutions in order to accelerate closure of waste tanks at the Savannah River Site (SRS) as part of the Modular Salt Processing (MSP) technology development program. Two ion exchange materials, spherical Resorcinol-Formaldehyde (RF) and engineered Crystalline Silicotitanate (CST), are being considered for use within the SCIX unit. Both ion exchange materials have been studied extensively and are known to have high affinities for cesium ions in caustic tank waste supernates. RF is an elutable organic resin and CST is a non-elutable inorganic material. Waste treatment processes developed for the two technologies will differ with regard to solutions processed, secondary waste streams generated, optimum column size, and waste throughput. Pertinent references, anticipated processing sequences for utilization in waste treatment, gaps in the available data, and technical comparisons will be provided for the two ion exchange materials to assist in technology selection for SCIX. The engineered, granular form of CST (UOP IE-911) was the baseline ion exchange material used for the initial development and design of the SRS SCIX process (McCabe, 2005). To date, in-tank SCIX has not been implemented for treatment of radioactive waste solutions at SRS. Since initial development and consideration of SCIX for SRS waste treatment an alternative technology has been developed as part of the River Protection Project Waste Treatment Plant (RPP-WTP) Research and Technology program (Thorson, 2006). Spherical RF resin is the baseline media for cesium removal in the RPP-WTP, which was designed for the treatment of radioactive waste supernates and is currently under construction in Hanford, WA

  13. LITERATURE REVIEWS TO SUPPORT ION EXCHANGE TECHNOLOGY SELECTION FOR MODULAR SALT PROCESSING

    International Nuclear Information System (INIS)

    This report summarizes the results of literature reviews conducted to support the selection of a cesium removal technology for application in a small column ion exchange (SCIX) unit supported within a high level waste tank. SCIX is being considered as a technology for the treatment of radioactive salt solutions in order to accelerate closure of waste tanks at the Savannah River Site (SRS) as part of the Modular Salt Processing (MSP) technology development program. Two ion exchange materials, spherical Resorcinol-Formaldehyde (RF) and engineered Crystalline Silicotitanate (CST), are being considered for use within the SCIX unit. Both ion exchange materials have been studied extensively and are known to have high affinities for cesium ions in caustic tank waste supernates. RF is an elutable organic resin and CST is a non-elutable inorganic material. Waste treatment processes developed for the two technologies will differ with regard to solutions processed, secondary waste streams generated, optimum column size, and waste throughput. Pertinent references, anticipated processing sequences for utilization in waste treatment, gaps in the available data, and technical comparisons will be provided for the two ion exchange materials to assist in technology selection for SCIX. The engineered, granular form of CST (UOP IE-911) was the baseline ion exchange material used for the initial development and design of the SRS SCIX process (McCabe, 2005). To date, in-tank SCIX has not been implemented for treatment of radioactive waste solutions at SRS. Since initial development and consideration of SCIX for SRS waste treatment an alternative technology has been developed as part of the River Protection Project Waste Treatment Plant (RPP-WTP) Research and Technology program (Thorson, 2006). Spherical RF resin is the baseline media for cesium removal in the RPP-WTP, which was designed for the treatment of radioactive waste supernates and is currently under construction in Hanford, WA

  14. Effect of NaCl on growth and ion relations in two salt-tolerant strains of Paxillus involutus

    Institute of Scientific and Technical Information of China (English)

    ZHANG Hua; WANG Mei-juan; LU Yan-jun; LI Li-si; Rosemarie LANGENFELD-HEYSER; Fritz EBERHARD; Andrea POLLE; LI Jing; CHEN Shao-liang; LU Cun-fu; WANG Rui-gang; DAI Song-xiang; ZHU Hui-juan; ZHANG Yun-xia; SHI Yong

    2008-01-01

    The effect of NaCl on growth, biomass and ion relations of two salt-tolerant isolates of Paxillus involutus, MAJ and NAU were investigated. The two Paxillus strains were exposed to the following concentrations of NaCl: 0, 100, 200 and 500 mmol·L-1. Growth of MAJ and NAU was enhanced by 100 mmol·L-1 NaCl but severely inhibited at the concentration of 500 mmol·L-1. NAU exhibited a greater capacity to exclude Na+ and Cl- under all salinity levels, whereas the salt-includer MAJ had a higher capacity in nutrient uptake under salt stress. The ratios Na+/K+, Na+/Ca2+ and Na+/Mg2+ in NaCl-treated MAJ and NAU did not increase at levels of 100 and 200 mmol·L-1 NaCl but markedly increased at 500 mmol·L-1. This suggests that the two strains, especially MAJ, enhanced nutrient uptake corresponding to the increased Na+ influx at moderate salinity. We conclude that both MAJ and NAU are able to tolerate 500 mmol·L-1 NaCl but there arc species-specific differences in retaining ionic homeostasis in the two Paxillus strains. NAU is a salt-excluder, MAJ is a salt-includer but retains a high capacity in nutrient selectivity under saline conditions. Their definite mechanisms to enhance salt tolerance of mycorrhizal hosts need further study.

  15. PC based electrolytes with LiDFOB as an alternative salt for lithium-ion batteries

    Science.gov (United States)

    Knight, Brandon M.

    Lithium-ion batteries (LIBs) have been greatly sought after as a source of renewable energy storage. LIBs have a wide range of applications including but not limited portable electronic devices, electric vehicles, and power tools. As a direct result of their commercial viability an insatiable hunger for knowledge, advancement within the field of LIBs has been omnipresent for the last two decades. However, there are set backs evident within the LIB field; most notably the limitations of standard electrolyte formulations and LiPF6 lithium salt. The standard primary carbonate of ethylene carbonate (EC) has a very limited operating range due to its innate physical properties, and the LiPF6 salt is known to readily decompose to form HF which can further degrade LIB longevity. The goal of our research is to explore the use of a new primary salt LiDFOB in conjunction with a propylene carbonate based electrolyte to establish a more flexible electrolyte formulation by constructing coin cells and cycling them under various conditions to give a clear understanding of each formulation inherent performance capabilities. Our studies show that 1.2M LiDFOB in 3:7 PC/EMC + 1.5% VC is capable of performing comparably to the standard 1.2M LiPF6 in 3:7 EC/EMC at 25°C and the PC electrolyte also illustrates performance superior to the standard at 55°C. The degradation of lithium manganese spinel electrodes, including LiNi 0.5Mn1.5O4, is an area of great concern within the field of lithium ion batteries (LIBs). Manganese containing cathode materials frequently have problems associated with Mn dissolution which significantly reduces the cycle life of LIB. Thus the stability of the cathode material is paramount to the performance of Mn spinel cathode materials in LIBs. In an effort to gain a better understanding of the stability of LiNi0.5 Mn1.5O4 in common LiPF6/carbonate electrolytes, samples were stored at elevated temperature in the presence of electrolyte. Then after storage both

  16. Titratable Macroions in Multivalent Electrolyte Solutions: Strong Coupling Dressed Ion Approach

    CERN Document Server

    Adzic, Natasa

    2016-01-01

    We present a theoretical description of the effect of polyvalent ions on the interaction between titratable macro-ions. The model system consists of two point-like macro-ions with dissociable sites, immersed in an asymmetric ionic mixture of monovalent and polyvalent salts. We formulate a {\\em dressed ion strong coupling theory}, based on the decomposition of the asymmetric ionic mixture into a weakly electrostatically coupled monovalent salt, and into polyvalent ions that are strongly electrostatically coupled to the titratable macro-ions. The charge of the macroions is not considered as fixed, but is allowed to respond to local bathing solution parameters (electrostatic potential, $pH$ of the solution, salt concentration) through a simple {\\em charge regulation} model. The approach presented, yielding an effective polyvalent-ion mediated interaction between charge-regulated macro-ions at various solution conditions, describes the strong coupling equivalent of the Kirkwood-Schumaker interaction.

  17. Ion Recognition Approach to Volume Reduction of Alkaline Tank Waste by Separation of Sodium Salts

    Energy Technology Data Exchange (ETDEWEB)

    Moyer, Bruce A.; Bonnesen, Peter V.; Custelcean, Radu; Delmau, Laetitia H.; Engle, Nancy L.; Kang, Hyun-Ah; Keever, Tamara J.; Marchand, Alan P.; Gadthula, Srinivas; Gore, Vinayak K.; Huang, Zilin; Sivappa, Rasapalli; Tirunahari, Pavan K.; Levitskaia, Tatiana G.; Lumetta, Gregg J.

    2005-09-26

    The purpose of this research involving collaboration between Oak Ridge National Laboratory (ORNL) and Pacific Northwest National Laboratory (PNNL) is to explore new approaches to the separation of sodium hydroxide, sodium nitrate, and other sodium salts from high-level alkaline tank waste. The principal potential benefit is a major reduction in disposed waste volume, obviating the building of expensive new waste tanks and reducing the costs of vitrification. Principles of ion recognition are being researched toward discovery of liquid-liquid extraction systems that selectively separate sodium hydroxide and sodium nitrate from other waste components. The successful concept of pseudo hydroxide extraction using fluorinated alcohols and phenols is being developed at ORNL and PNNL toward a greater understanding of the controlling equilibria, role of solvation, and of synergistic effects involving crown ethers. Synthesis efforts are being directed toward enhanced sodium binding by crown ethers, both neutral and proton-ionizable. Studies with real tank waste at PNNL will provide feedback toward solvent compositions that have promising properties.

  18. New boron based salts for lithium-ion batteries using conjugated ligands.

    Science.gov (United States)

    Jankowski, P; Wieczorek, W; Johansson, P

    2016-06-28

    A new anion design concept, based on combining a boron atom as the central atom and conjugated systems as ligands, is presented as a route for finding alternative Li-salts for lithium-ion batteries. The properties of a wide range of novel anions designed in this way have been evaluated by DFT calculations focusing on three different fundamental success factors/measures: the strength of the cation-anion interaction, ultimately determining both the solubility and the ionic conductivity, the oxidation limit, determining their possible use vs. high voltage cathodes, and the reduction stability, revealing a possible role of the anion in the SEI-formation at the anode. For a few anions superior properties vs. today's existing or suggested anions are predicted, especially the very low cation-anion interaction strengths are promising features. The design route itself is shown to be versatile in determining the correlation between different choices of ligands and the resulting overall properties - where the most striking feature is the decreased lithium cation interaction energy upon using the (1Z,3Z)-buta-1,3-diene-1,2,3,4-tetracarbonitrile ligands. This also opens avenues for the further design of novel anions beyond those with a boron central atom. PMID:27253752

  19. Simultaneous removal of organic matter and salt ions from saline wastewater in bioelectrochemical systems

    KAUST Repository

    Kim, Younggy

    2013-01-01

    A new bioelectrochemical system is proposed for simultaneous removal of salinity and organic matter. In this process, exoelectrogenic microorganisms oxidize organic matter and transfer electrons to the anode, hydrogen is evolved at the cathode by supplying additional voltage, and salt is removed from the wastewater due to the electric potential generated and the use of two ion-exchange membranes. Salinity removal (initial conductivity ~40mS/cm) increased from 21 to 84% by increasing the substrate (sodium acetate) from 2 to 8g/L. A total of 72-94% of the chemical oxygen demand was degraded in the anode and cathode chambers, with 1-4% left in the anode chamber and the balance lost through the anion-exchange membrane into the concentrate waste chamber. The maximum hydrogen production rate was 3.6m3-H2/m3-electrolyte per day at an applied potential of 1.2V. The Coulombic efficiency was ~100%, while the cathode recovery varied from 57 to 100%, depending on the extent of methanogenesis. Exoelectrogenic microbes generated high current densities (7.8mA/cm2) at ≤36g/L of total dissolved solids, but >41g/L eliminated current. These results provide a new method for achieving simultaneous removal of salinity and organic matter from a saline wastewater with H2 production. © 2012 Elsevier B.V.

  20. Secretion by the nasal salt glands of two insectivorous lizard species is initiated by an ecologically relevant dietary ion, chloride.

    Science.gov (United States)

    Hazard, Lisa C; Lechuga, Claudia; Zilinskis, Stephanie

    2010-08-01

    Salt glands are used by some vertebrates to excrete hyperosmotic NaCl or KCl solutions in response to dietary salt loads. Control of secretion varies across taxa; some secrete in response to osmotic challenges while others secrete in response to specific dietary ions. We hypothesized that differences in control could be related to different diet-related selective pressures on herbivorous, marine, and insectivorous species. We studied control of secretion and flexibility of cation (sodium or potassium) and anion (chloride or bicarbonate) secretion in two insectivorous lizard species, Schneider's skinks (Eumeces schneideri, Scincidae) and green anoles (Anolis carolinensis, Polychrotidae). Lizards were injected daily for four days with combinations of cations (potassium, sodium, and histidine control) and anions (chloride and acetate control), isoosmotic saline, or sham injection. Secretions were collected daily and analyzed for sodium, potassium, and chloride. Both species secreted only in response to chloride; sodium appeared to have a slight inhibitory effect. Regardless of cation load, skinks secreted a combination of potassium and sodium, while anoles secreted solely potassium. In both species, total cation secretion was matched closely by chloride; very little bicarbonate was secreted. As predicted, secretion in insectivorous lizards was initiated by the dietary ion ecologically most important for these species, chloride, which otherwise cannot be excreted without significant water loss (unlike the cations, which may be excreted as insoluble urate salts). This gives further support to the hypothesis that ecological factors drive the evolution of control mechanisms in lizard salt glands. PMID:20623801

  1. Membrane ion transport in erythrocytes of salt hypertensive Dahl rats and their F2 hybrids: the importance of cholesterol

    Czech Academy of Sciences Publication Activity Database

    Vokurková, Martina; Dobešová, Zdenka; Kuneš, Jaroslav; Zicha, Josef

    2003-01-01

    Roč. 26, č. 5 (2003), s. 397-404. ISSN 0916-9636 R&D Projects: GA ČR GA305/00/1638; GA MŠk LN00A069 Institutional research plan: CEZ:AV0Z5011922 Keywords : ion transport * salt hypertension * plasma lipids Subject RIV: FA - Cardiovascular Diseases incl. Cardiotharic Surgery Impact factor: 2.013, year: 2003

  2. Influences of nitrification inhibitor 3,4-dimethyl pyrazole phosphate on nitrogen and soil salt-ion leaching

    Institute of Scientific and Technical Information of China (English)

    YU Qiaogang; YE Xuezhu; CHEN Yingxu; ZHANG Zhijian; TIAN Guangming

    2008-01-01

    An undisturbed heavy clay soil column experiment was conducted to examine the influence of the new nitrification inhibitor,3,4-dimethylpyrazole phosphate (DMPP),on nitrogen and soil salt-ion leaching.Regular urea was selected as the nitrogen source in the soil.The results showed that the cumulative leaching losses of soil nitrate-N under the treatment of urea with DMPP were from 57.5% to 63.3% lower than those of the treatment of urea without DMPP.The use of nitrification inhibitors as nitrate leaching retardants may be a proposal in regulations to prevent groundwater contaminant.However,there were no great difference between urea and urea with DMPP treatments on ammonium-N leaching.Moreover,the soil salt-ion leaching losses of Ca2+,Mg2+,K+,and Na+ were reduced from 26.6% to 28.8%,21.3% to 27.8%,33.3% to 35.5%,and 21.7% to 32.1%,respectively.So,the leaching losses of soil salt-ion were declined for nitrification inhibitor DMPP addition,being beneficial to shallow groundwater protection and growth of crop.These results indicated the possibility of ammonium or ammonium producing compounds using nitrification inhibitor DMPP to control the nitrate and nutrient cation leaching losses,minimizing the risk of nitrate pollution in shallow groundwater.

  3. Salt Tolerance

    OpenAIRE

    Xiong, Liming; Zhu, Jian-Kang

    2002-01-01

    Studying salt stress is an important means to the understanding of plant ion homeostasis and osmo-balance. Salt stress research also benefits agriculture because soil salinity significantly limits plant productivity on agricultural lands. Decades of physiological and molecular studies have generated a large body of literature regarding potential salt tolerance determinants. Recent advances in applying molecular genetic analysis and genomics tools in the model plant Arabidopsis thaliana are sh...

  4. The optimal composition of sorbents on the basis of iso- and hetero-polyacid salts for selective concentration of inorganic ions

    International Nuclear Information System (INIS)

    Present article is devoted to selection of optimal composition of sorbents on the basis of iso- and hetero-polyacid salts for selective concentration of inorganic ions. Thus, several options are proposed and considered.

  5. Hydroxy double salts loaded with bioactive ions: Synthesis, intercalation mechanisms, and functional performance

    Science.gov (United States)

    Kaassis, Abdessamad Y. A.; Xu, Si-Min; Guan, Shanyue; Evans, David G.; Wei, Min; Williams, Gareth R.

    2016-06-01

    The intercalation of the anions of diclofenac (Dic), naproxen (Nap), and valproic acid (Val) into three hydroxy double salts (HDSs) has been explored in this work. Experiments were performed with [Co1.2Zn3.8(OH)8](NO3)2·2H2O (CoZn-NO3), [Ni2Zn3(OH)8](NO3)2·2H2O (NiZn-NO3) and [Zn5(OH)8](NO3)2·2H2O (Zn-NO3). It proved possible to intercalate diclofenac and naproxen into all three HDSs. In contrast, Val could be intercalated into CoZn-NO3 but when it was reacted with Zn-NO3 the HDS structure was destroyed, and the product comprised ZnO. Successful intercalation was verified by X-ray diffraction, IR spectroscopy, and elemental microanalysis. Molecular dynamics simulations showed the Dic and Nap ions to arrange themselves in an "X" shape in the interlayer space, forming a bilayer. Val was found to adopt a position with its aliphatic groups parallel to the HDS layer, again in a bilayer. In situ time resolved X-ray diffraction experiments revealed that intercalation of Dic and Nap into CoZn-NO3 and Zn-NO3 is mechanistically complex, with a number of intermediate phases observed. In contrast, the intercalation of all three guests into NiZn-NO3 and of Val into CoZn-NO3 are simple one step reactions proceeding directly from the starting material to the product. The HDS-drug composites were found to have sustained release profiles.

  6. Ion exchange method for calcium isolation from solutions of zinc, cadmium, and cobalt salts

    International Nuclear Information System (INIS)

    A method for isolating impurity amounts of calcium from zinc, cadmium and cobalt salts has been suggested. The method consists in dissolution of the above-mentioned metal salts in ammonia solution, selective sorption of calcium impurities from solutions prepared on carboxylic cationite with subsequent calcium desorption by mineral acid solution. 4 refs.; 2 figs

  7. Lithium salt with a super-delocalized perfluorinated sulfonimide anion as conducting salt for lithium-ion cells: Physicochemical and electrochemical properties

    Science.gov (United States)

    Zhang, Heng; Han, Hongbo; Cheng, Xiaorong; Zheng, Liping; Cheng, Pengfei; Feng, Wenfang; Nie, Jin; Armand, Michel; Huang, Xuejie; Zhou, Zhibin

    2015-11-01

    Lithium salt with a super-delocalized imide anion, namely (trifluoromethane(S-trifluoromethanesulfonylimino)sulfonyl) (trifluoromethanesulfonyl)imide ([CF3SO(=NSO2CF3)2]-), [sTFSI]-), has been prepared and studied as conducting salt for Li-ion cells. The fundamental physicochemical and electrochemical properties of neat Li[sTFSI] and its carbonate-based liquid electrolyte have been characterized with various chemical and electrochemical tools. Li[sTFSI] shows a low melting point at 118 °C, and is thermally stable up to 300 °C without decomposition on the spectra of differential scanning calorimetry-thermogravimetry-mass spectrometry (DSC-TG-MS). The electrolyte of 1.0 M (mol dm-3) Li[sTFSI] in ethylene carbonate (EC)/ethyl-methyl-carbonate (EMC) (3:7, v/v) containing 0.3% water does not show any hydrolytic decomposition on the spectra of 1H and 19F NMR, after storage at 85 °C for 10 days. The conductivities of 1.0 M Li[sTFSI]-EC/EMC (3:7, v/v) are slightly lower than those of Li[(CF3SO2)2N] (LiTFSI), but higher than those of Li[(C2F5SO2)2N] (LiBETI). The electrochemical behavior of Al foil in the Li[sTFSI]-based electrolyte has been investigated by using cyclic voltammetry and chronoamperometry, and scanning electron microscope (SEM). It is illustrated that Al metal does not corrode in the high potential region (3-5 V vs. Li/Li+) in the Li[sTFSI]-based electrolyte. On Pt electrode, the Li[sTFSI]-based electrolyte is highly resistant to oxidation (ca. 5 V vs. Li/Li+), and is also resistant to reduction to allow Li deposition and stripping. The applicability of Li[sTFSI] as conducting salt for Li-ion cells has been tested using graphite/LiCoO2 cells. It shows that the cell with Li[sTFSI] displays better cycling performance than that with LiPF6.

  8. Liquid electrolyte based on lithium bis-fluorosulfonyl imide salt: Aluminum corrosion studies and lithium ion battery investigations

    Energy Technology Data Exchange (ETDEWEB)

    Abouimrane, A.; Ding, J.; Davidson, I.J. [Institute for Chemical Process and Environmental Technology, National Research Council Canada, 1200 Montreal Road, Ottawa K1A 0R6 (Canada)

    2009-04-01

    The performance of a liquid electrolyte composed of lithium bis-fluorosulfonyl imide (LiSFI) in a 1:1 volume of ethylene carbonate and dimethyl carbonate is evaluated for use in lithium ion batteries. Imide salts offer the benefits of higher thermal stability and could provide a safer alternative to LiPF{sub 6} which is prone to the formation of HF. However, the most studied lithium imide salt, lithium bis(trifluoromethanesulfonyl) imide, is well known to have a problem with corrosion of aluminum which is commonly used as the cathode current collector. Consequently, the corrosion properties of liquid electrolytes based on lithium bis-fluorosulfonyl imide are also investigated. (author)

  9. Near-surface density profiling of Fe ion irradiated Si (100) using extremely asymmetric x-ray diffraction by variation of the wavelength

    International Nuclear Information System (INIS)

    In this work, we report on correlations between surface density variations and ion parameters during ion beam-induced surface patterning process. The near-surface density variations of irradiated Si(100) surfaces were investigated after off-normal irradiation with 5 keV Fe ions at different fluences. In order to reduce the x-ray probing depth to a thickness below 5 nm, the extremely asymmetrical x-ray diffraction by variation of wavelength was applied, exploiting x-ray refraction at the air-sample interface. Depth profiling was achieved by measuring x-ray rocking curves as function of varying wavelengths providing incidence angles down to 0°. The density variation was extracted from the deviations from kinematical Bragg angle at grazing incidence angles due to refraction of the x-ray beam at the air-sample interface. The simulations based on the dynamical theory of x-ray diffraction revealed that while a net near-surface density decreases with increasing ion fluence which is accompanied by surface patterning, there is a certain threshold of ion fluence to surface density modulation. Our finding suggests that the surface density variation can be relevant with the mechanism of pattern formation.

  10. Strain evolution in Si substrate due to implantation of MeV ion observed by extremely asymmetric x-ray diffraction

    International Nuclear Information System (INIS)

    We studied the strain introduced in a Si(111) substrate due to MeV ion implantation using extremely asymmetric x-ray diffraction and measured the rocking curves of asymmetrical 113 diffraction for the Si substrates implanted with a 1.5 MeV Au2+ ion at fluence values of 1x1013, 5x1013, and 1x1014/cm2. The measured curves consisted of a bulk peak and accompanying subpeak with an interference fringe. The positional relationship of the bulk peak to the subpeak and the intensity variation of those peaks with respect to the wavelengths of the x rays indicated that crystal lattices near the surface were strained; the lattice spacing of surface normal (111) planes near the surface was larger than that of the bulk. Detailed strain profiles along the depth direction were successfully estimated using a curve-fitting method based on Darwin's dynamical diffraction theory. Comparing the shapes of resultant strain profiles, we found that a strain evolution rapidly occurred within a depth of ∼300 nm at fluence values between 1x1013 and 5x1013/cm2. This indicates that formation of the complex defects progressed near the surface when the fluence value went beyond a critical value between 1x1013 and 5x1013/cm2 and the defects brought a large strain to the substrate.

  11. Changes in Transcript Related to Osmosis and Intracellular Ion Homeostasis in Paulownia tomentosa under Salt Stress

    OpenAIRE

    Fan, Guoqiang; Wang, Limin; Deng, Minjie; Zhao, Zhenli; Dong, Yanpeng; Zhang, Xiaoshen; Li, Yongsheng

    2016-01-01

    Paulownia tomentosa is an important economic and greening tree species that is cultivated widely, including salt environment. Our previous studies indicated its autotetraploid induced by colchicine showed better stress tolerance, but the underlying molecular mechanism related to ploidy and salt stress is still unclear. To investigate this issue, physiological measurements and transcriptome profiling of diploid and autotetraploid plants untreated and treated with NaCl were performed. Through t...

  12. The influence of salt type on the retention of bovine serum albumin in ion-exchange chromatography

    DEFF Research Database (Denmark)

    Al-Jibbouri, Sattar

    2007-01-01

    In this paper, an analysis of the influence of the salt types, NaCl, NaCH"3COO, Na"2SO"4 and Na"3C"6H"5O"7, on the isocratic retention behaviour of bovine serum albumin (BSA) on two anion-exchangers media (Source 30Q and TSK Gel Super Q 5 PW) has been presented. The retention data demonstrated that...... the mechanism of protein retention in ion-exchange chromatography (IEC) involves interactions between the protein solute, the mobile phase constituents and the stationary phase. The effect of protein activity coefficient in the mobile phase on the protein retention volumes is verified....

  13. The 2-D Ion Chromatography Development and Application: Determination of Sulfate in Formation Water at Pre-Salt Region

    Science.gov (United States)

    Tonietto, G. B.; Godoy, J. M.; Almeida, A. C.; Mendes, D.; Soluri, D.; Leite, R. S.; Chalom, M. Y.

    2015-12-01

    Formation water is the naturally-occurring water which is contained within the geological formation itself. The quantity and quality of the formation water can both be problematic. Over time, the water volume should decrease as the gas volumes increase. Formation water has been found to contain high levels of Cl, As, Fe, Ba, Mn, PAHs and may even contain naturally occurring radioactive materials. Chlorides in some cases have been found to be in excess of four-five times the level of concentrations found in the ocean. Within the management of well operation, there is sulfate between the analytes of greatest importance due to the potential for hydrogen sulphide formation and consequent corrosion of pipelines. As the concentration of sulfate in these waters can be less than n times that of chloride, a quantitative determination, using the technique of ion chromatography, constitutes an analytical challenge. This work aimed to develop and validate a method for the determination of sulphate ions in hyper-saline waters coming from the oil wells of the pre-salt, using 2D IC. In 2D IC the first column can be understood as a separating column, in which the species with retention times outside a preset range are discarded, while those belonging to this range are retained in a pre-concentrator column to further injecting a second column, the second dimension in which occurs the separation and quantification of the analytes of interest. As the chloride ions have a retention time lower than that of sulfate, a method was developed a for determining sulfate in very low range (mg L-1) by 2D IC, applicable to hypersaline waters, wherein the first dimension is used to the elimination of the matrix, ie, chloride ions, and the second dimension utilized in determining sulfate. For sulphate in a concentration range from 1.00 mg L-1 was obtained an accuracy of 1.0%. The accuracy of the method was tested by the standard addition method different samples of formation water in the pre-salt

  14. A Systematic Investigation of Quaternary Ammonium Ions as Asymmetric Phase Transfer Catalysts. Application of Quantitative Structure Activity/Selectivity Relationships

    OpenAIRE

    Denmark, Scott E.; Gould, Nathan D.; Wolf, Larry M

    2011-01-01

    While the synthetic utility of asymmetric phase transfer catalysis continues to expand, the number of proven catalyst types and design criteria remains limited. At the origin of this scarcity is a lack in understanding of how catalyst structural features affect the rate and enantioselectivity of phase transfer catalyzed reactions. Described in this paper is the development of quantitative structure-activity relationships (QSAR) and -selectivity relationships (QSSR) for the alkylation of a pro...

  15. Adiabatic and sudden interaction potentials in the fusion-fission of heavy ion collisions: Asymmetric target-projectile combinations

    International Nuclear Information System (INIS)

    It is now well known that many reactions giving measurable fusion cross-sections also show a fission of the compound system formed, similar to the low energy fission of the known fissioning nuclei. Recently, both the fusion excitation functions and the mass equilibration in the fragmentation of the composite system were measured for a large number of systems with 94208Pb on different targets of 26Mg, 48Ca, 50Ti, 52Cr, 58Fe and 64Ni. From a theoretical point of view, it is relevant to ask the question: how do the colliding nuclei fuse and then why does the compound system formed fission instead of going to the ground state to give a stable system. In this Letter, we attempt to show that the fusion of asymmetric colliding nuclei is due to the overcoming of the interaction barriers in adiabatic potentials and the fission of the compound system should perhaps occur as a sudden process, like the one in the spontaneous fission phenomenon. We have made our calculations for the compound systems with 102<=Z<=110 and for the asymmetric target-projectile combinations of the experiments of Ref. 1, using the fragmentation theory whose basis is the asymmetric two-centre shell model

  16. Elucidating the structures and cooperative binding mechanism of cesium salts to the multitopic ion-pair receptor through density functional theory calculations.

    Science.gov (United States)

    Sadhu, Biswajit; Sundararajan, Mahesh; Velmurugan, Gunasekaran; Venuvanalingam, Ponnambalam

    2015-09-21

    Designing new and innovative receptors for the selective binding of radionuclides is central to nuclear waste management processes. Recently, a new multi-topic ion-pair receptor was reported which binds a variety of cesium salts. Due to the large size of the receptor, quantum chemical calculations on the full ion-pair receptors are restricted, thus the binding mechanisms are not well understood at the molecular level. We have assessed the binding strengths of various cesium salts to the recently synthesized multi-topic ion-pair receptor molecule using density functional theory based calculations. Our calculations predict that the binding of cesium salts to the receptor predominantly occurs via the cooperative binding mechanism. Cesium and the anion synergistically assist each other to bind favorably inside the receptor. Energy decomposition analysis on the ion-pair complexes shows that the Cs salts are bound to the receptor mainly through electrostatic interactions with small contribution from covalent interactions for large ionic radius anions. Further, QTAIM analysis characterizes the importance of different inter-molecular interactions between the ions and the receptor inside the ion-pair complexes. The role of the crystallographic solvent molecule contributes significantly by ~10 kcal mol(-1) to the overall binding affinities which is quite significant. Further, unlike the recent molecular mechanics (MM) calculations, our calculated binding affinity trends for various Cs ion-pair complexes (CsF, CsCl and CsNO3) are now in excellent agreement with the experimental binding affinity trends. PMID:26227949

  17. Breeding of sunflower for salt tolerance: estimation of ion concentration in sunflower (helianthus annuus L.) seedling

    International Nuclear Information System (INIS)

    The experiment was conducted to estimate variability and effect of three artificially induced electrical conductivities on ions concentrations in sunflower seedling leaves. There was no exception in case of CT concentration and all the genotypes showed increase in CT concentration in their seeding leaves, however, some increase in salinity. Similarly Na ion did not show any increase while some genotypes even decreased Na ion concentration in their seedling leaves with increase while some genotypes even decreased Na ion concentration in their seedling leaves with increase in salinity. Potassium ion concentration decrease with increase in salinity but some genotypes showed the ability to maintain K ion concentration in seedling leaves. Thus there appeared two mechanisms of salinity tolerance in sunflower; either by maintaining Na+ at lower level or K ion at higher level and keeping K/sup +/Na/sup +/ ratio favourable in young growing seeding leaves. (author)

  18. Lithium difluoro(sulfato)borate as a novel electrolyte salt for high-temperature lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • LiBF2SO4 was investigated as a novel electrolyte salt for advanced high-temperature LIBs. • At 80 °C, LiBF2SO4-EC/DMC electrolyte favourably facilitates the formation of a thermal stable, effective and conductive interface film on the surface of carbonaceous anode. • At 80 °C, LiBF2SO4-EC/DMC electrolyte exerts several advantages, such as stable cycling performance, low polarization resistance, and good rate performance in LiFePO4/Li cells. - Abstract: High-temperature electrochemical behaviors of the novel salt named lithium difluoro(sulfato)borate (LiBF2SO4) were studied by employment of ethylene carbonate (EC) and dimethyl carbonate (DMC) as mixed solvents. In Li/MCMB (mesophase carbon microbeads) cells at 80 °C, LiBF2SO4-EC/DMC electrolyte favourably facilitates the formation of a thermal stable, effective and conductive interface film on the surface of carbonaceous anode. Besides, in LiFePO4/Li cells at 80 °C, LiBF2SO4-EC/DMC electrolyte exerts several advantages, such as stable cycling performance, low polarization resistance, and good rate performance. It suggests that LiBF2SO4 is an excellent candidate salt for advanced high-temperature lithium-ion batteries

  19. Thermal stability of LiPF 6 salt and Li-ion battery electrolytes containing LiPF 6

    Science.gov (United States)

    Yang, Hui; Zhuang, Guorong V.; Ross, Philip N.

    The thermal stability of the neat lithium hexafluorophosphate (LiPF 6) salt and of 1 molal (m) solutions of LiPF 6 in prototypical Li-ion battery solvents was studied with thermogravimetric analysis (TGA) and on-line Fourier transform infrared (FTIR). Pure LiPF 6 salt is thermally stable up to 107 °C in a dry inert atmosphere, and its decomposition path is a simple dissociation producing lithium fluoride (LiF) as solid and PF 5 as gaseous products. In the presence of water (300 ppm) in the carrier gas, its decomposition onset temperature is lowered as a result of direct thermal reaction between LiPF 6 and water vapor to form phosphorous oxyfluoride (POF 3) and hydrofluoric acid (HF). No new products were observed in 1 m solutions of LiPF 6 in ethylene carbonate (EC), dimethyl carbonate (DMC) and ethyl methyl carbonate (EMC) by on-line TGA-FTIR analysis. The storage of the same solutions in sealed containers at 85 °C for 300-420 h did not produce any significant quantity of new products as well. In particular, no alkylflurophosphates were found in the solutions after storage at elevated temperature. In the absence of either an impurity like alcohol or cathode active material that may (or may not) act as a catalyst, there is no evidence of thermally induced reaction between LiPF 6 and the prototypical Li-ion battery solvents EC, PC, DMC or EMC.

  20. Syntheses and Application of All-lithium Salts of Heteropolyacid as Electrolyte of Lithium-ion Battery

    Institute of Scientific and Technical Information of China (English)

    CHEN Ya-guang; WANG Cun-guo; ZHANG Xi-yan; XIE De-min; WANG Rong-shun

    2004-01-01

    The all-lithium salts of heteropoly acid LixXM12O40(HPA-Li)(X=P, Si; M=Mo, W) were obtained via ion exchange and characterized by means of IR and UV spectroscopies, TG and elemental analyses. The conductivity of the electrolytic solution consisting of Li3PW12O40 and PC/DME mixing solvent(1/2.5, volume ratio) is up to 7.2×10-2 S/cm, being higher than that of LiClO4 as the electrolyte. The all-lithium salts were used as electrolytes in secondary lithium-ion batteries. The discharge capacity of the PAS/Li batteries with Li3PW12O40 electrolyte solutions reaches to 148 (mA*h)/g and the cyclic life is up to 380 times, much better than those of commercialized products with LiClO4 and LiAsF6 as electrolytes.

  1. Fully Ir(iii) tetrazolate soft salts: the road to white-emitting ion pairs.

    Science.gov (United States)

    Fiorini, Valentina; D'Ignazio, Andrea; Magee, Karen D M; Ogden, Mark I; Massi, Massimiliano; Stagni, Stefano

    2016-02-28

    The first examples of anionic Ir(iii) bis-tetrazolate complexes and their combination with a cationic Ir(iii)tetrazole derivative forming "fully tetrazolate" Ir(iii) based soft salts as O2-sensitive white emitters are described herein. PMID:26837780

  2. Tomato salt tolerance: Impact of grafting and water composition on yield and ion relations

    Science.gov (United States)

    We evaluated the salt tolerance of tomato cv Big Dena under both non-grafted 2 conditions and when grafted on Maxifort rootstock, under a series of 5 salinity levels and two irrigation water composition types. The salinity levels of the irrigation water were -0.03, -0.15, -0.30, -0.45, and -0.60 MPa...

  3. Electro-membrane reactor for separation and in situ ion substitution of glutamic acid from its sodium salt

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Mahendra; Tripathi, Bijay P. [Electro-Membrane Processes Division, Central Salt and Marine Chemicals Research Institute, Council of Scientific and Industrial Research (CSIR), G. B. Marg, Bhavnagar 364002, Gujarat (India); Shahi, Vinod K. [Electro-Membrane Processes Division, Central Salt and Marine Chemicals Research Institute, Council of Scientific and Industrial Research (CSIR), G. B. Marg, Bhavnagar 364002, Gujarat (India)], E-mail: vkshahi@csmcri.org

    2009-08-30

    An electro-membrane reactor with four compartments (EMR-4) (anolyte, catholyte and comp. 1 and 2) based on in-house-prepared cation- and anion-exchange membrane (CEM and AEM, respectively) was developed to achieve separation and recovery of glutamic acid (GAH) from its sodium salt by in situ ion substitution and acidification. The physicochemical and electrochemical properties of CEM and AEM were characterized and its suitability was assessed in operating environment. The separation of GA{sup -} from the mixture of nonionic organic compounds and further ion substitution was achieved by EMR-4. But the higher energy consumption (5.75 kWh/kg of GAH produced), low current efficiency (50.5%) and recovery of GAH (57.2%) in this process were main obstacles for the industrial exploration of the process. Latter, electro-membrane reactor with three compartments (EMR-3) (anolyte, catholyte and central compartment) was developed based on CEMs for only in situ ion substitution of GANa to achieve GAH, in which GA{sup -} was not allowed for electro-migration from its feed compartment. CE and recovery of GAH were close to 73% and 96% that indicate the suitability of the EMR-3 process for industrial application over the EMR-4. It was concluded that EMR-3 was efficient as compared to EMR-4 for separation and recovery of GAH from fermentation broth by in situ ion substitution in eco-friendly manner.

  4. Electro-membrane reactor for separation and in situ ion substitution of glutamic acid from its sodium salt

    International Nuclear Information System (INIS)

    An electro-membrane reactor with four compartments (EMR-4) (anolyte, catholyte and comp. 1 and 2) based on in-house-prepared cation- and anion-exchange membrane (CEM and AEM, respectively) was developed to achieve separation and recovery of glutamic acid (GAH) from its sodium salt by in situ ion substitution and acidification. The physicochemical and electrochemical properties of CEM and AEM were characterized and its suitability was assessed in operating environment. The separation of GA- from the mixture of nonionic organic compounds and further ion substitution was achieved by EMR-4. But the higher energy consumption (5.75 kWh/kg of GAH produced), low current efficiency (50.5%) and recovery of GAH (57.2%) in this process were main obstacles for the industrial exploration of the process. Latter, electro-membrane reactor with three compartments (EMR-3) (anolyte, catholyte and central compartment) was developed based on CEMs for only in situ ion substitution of GANa to achieve GAH, in which GA- was not allowed for electro-migration from its feed compartment. CE and recovery of GAH were close to 73% and 96% that indicate the suitability of the EMR-3 process for industrial application over the EMR-4. It was concluded that EMR-3 was efficient as compared to EMR-4 for separation and recovery of GAH from fermentation broth by in situ ion substitution in eco-friendly manner.

  5. Catalytic Asymmetric Synthesis of Both Enantiomers of 4‑Substituted 1,4-Dihydropyridines with the Use of Bifunctional Thiourea-Ammonium Salts Bearing Different Counterions

    Directory of Open Access Journals (Sweden)

    Kohzo Yoshida

    2010-11-01

    Full Text Available Organoammonium salts composed of a Brønsted acid and an anilinothiourea promoted the Michael addition of β-keto esters and α,β-unsaturated aldehydes in the presence of primary amines to give functionalized 1,4-dihydropyridines enantioselectively. With the use of the different Brønsted acids such as DFA and HBF4 with the same bifunctional thiourea, both enantiomers of 4-substituted 1,4-dihydropyridine were synthesized from the same starting materials.

  6. Titratable macroions in multivalent electrolyte solutions: Strong coupling dressed ion approach

    Science.gov (United States)

    Adžić, Nataša; Podgornik, Rudolf

    2016-06-01

    We present a theoretical description of the effect of polyvalent ions on the interaction between titratable macroions. The model system consists of two point-like macroions with dissociable sites, immersed in an asymmetric ionic mixture of monovalent and polyvalent salts. We formulate a dressed ion strong coupling theory, based on the decomposition of the asymmetric ionic mixture into a weakly electrostatically coupled monovalent salt and into polyvalent ions that are strongly electrostatically coupled to the titratable macro-ions. The charge of the macroions is not considered as fixed, but is allowed to respond to local bathing solution parameters (electrostatic potential, pH of the solution, and salt concentration) through a simple charge regulation model. The approach presented, yielding an effective polyvalent-ion mediated interaction between charge-regulated macroions at various solution conditions, describes the strong coupling equivalent of the Kirkwood-Schumaker interaction.

  7. The salts of chloronium ions R-Cl(+)-R (R = CH3 or CH2Cl): formation, thermal stability, and interaction with chloromethanes.

    Science.gov (United States)

    Stoyanov, Evgenii S

    2016-05-14

    The interaction of CH3Cl/CD3Cl or CH2Cl2/CD2Cl2 with the carborane acid H(CHB11Cl11) (abbreviated as H{Cl11}) generates the salts of CH3-{Cl11} and CH2Cl-{Cl11} and their deuterio analogs, respectively, which are analogs of the salts of asymmetric chloronium cations. Next, salts of chloronium cations CH3-Cl(+)-CH3, ClCH2-Cl(+)-CH2Cl, and ClCH2-Cl(+)-CH3 and their deuterio analogs were obtained from the above compounds. The asymmetric ClCH2-Cl(+)-CH3 cation was found to be unstable, and at ambient temperature, slowly disproportionated into symmetric cations (CH3)2Cl(+) and (CH2Cl)2Cl(+). At a high temperature (150 °C), disproportionation was completed within 5 minutes, and the resulting cations further decomposed into CH3-{Cl11} and CH2Cl-{Cl11}. The molecular fragment ClCH2-(X) of the compounds (X = {Cl11}, -Cl(+)-CH2Cl, or -Cl(+)-CH3) is involved in exchange reactions with CH2Cl2 and CHCl3, converting into CH3-(X) with the formation of chloroform and CCl4, respectively. PMID:27104946

  8. Ion exchange reactions in amorphous and crystalline aluminium silicates from solution of cerium salts

    International Nuclear Information System (INIS)

    Reactions of ion-exchange of Na+ by Ce3+ and NH4+ on the zeolite containing catalyst, amorphous silica alumina and zeolite Y have been studied. The cerium cations are shown to be exchanged by the Na+ cations with more selectivity than the anmonia cations. In the case of the zeolite containing catalyst and amorphous silica alumina the region of the staggered ion-exchange from the mixture of the solutions of cerium and ammonium sulphates was been detected. This is explained by the formation fo cerium complexes with the sulphate ions

  9. The salt and lipid composition of model cheeses modifies in-mouth flavour release and perception related to the free sodium ion content.

    Science.gov (United States)

    Boisard, Lauriane; Andriot, Isabelle; Martin, Christophe; Septier, Chantal; Boissard, Vanessa; Salles, Christian; Guichard, Elisabeth

    2014-02-15

    Reducing salt and lipid levels in foodstuffs without any effect on acceptability is a major challenge, particularly because of their interactions with other ingredients. This study used a multimodal approach to understand the effects of changes to the composition of model cheeses (20/28, 24/24, 28/20 lipid/protein ratios, 0% and 1% added NaCl) on sodium ion mobility ((23)Na NMR), in-mouth sodium release and flavour perception. An increase in the salt content decreased cheese firmness and perceived hardness, and increased sodium ion mobility, in vivo sodium release and both saltiness and aroma perception. With the same amount of salt, a lower lipid/protein ratio increased the firmness of the cheeses, perceived hardness, and decreased sodium ion mobility, in vivo sodium release, saltiness and aroma perception. These findings suggest on one hand that it could be possible to increase saltiness perception by varying cheese composition, thus inducing differences in sodium ion mobility and in free sodium ion concentration, leading to differences in in-mouth sodium release and saltiness perception, and on the other hand that the reformulation of foods in line with health guidelines needs to take account of both salt content and the lipid/protein ratio. PMID:24128499

  10. Preparation and electrochemical performance of polyphosphazene based salt-in-polymer electrolyte membranes for lithium ion batteries

    Science.gov (United States)

    Jankowsky, S.; Hiller, M. M.; Wiemhöfer, H.-D.

    2014-05-01

    This work presents a detailed study of the electrochemical performance of polyphosphazene based electrolyte membranes consisting of a linear polymer with -(Ndbnd PR2)- units, grafted with ethylene oxide side chains of the type R = -(OCH2CH2)3OCH3 and containing LiTFSI and LiBOB as dissolved lithium salts. The average molecular weight was 105 g mol-1. Mechanical stability was achieved by UV induced in-situ cross-linking of the thin polymer electrolyte films. Favorable properties of this type of polymer electrolytes are the good thermal and electrochemical stability of the electrolyte membranes, the broad electrochemical stability window ranging between 0 V and 4.7 V versus the Li/Li+ reference and a very good interface stability at lithium metal electrodes where a stable SEI was formed during initial contact. Total ionic conductivities up to 10-4 S cm-1 were measured at 30 °C. The transference numbers of lithium ions at 50 °C ranged between 0.06 and 0.07 and hence are lower by a factor of about three as compared to other typical polymer electrolytes. Nevertheless, the partial lithium ion conductivity estimated from the product of total conductivity and lithium ion transference number is as high or slightly higher compared to PEO based polymer electrolytes.

  11. Dietary salt loading and ion-poor water exposure provide insight into the molecular physiology of the rainbow trout gill epithelium tight junction complex.

    Science.gov (United States)

    Kolosov, Dennis; Kelly, Scott P

    2016-08-01

    This study utilized dietary salt loading and ion-poor water (IPW) exposure of rainbow trout (Oncorhynchus mykiss) to further understand the role of fish gill epithelium tight junction (TJ) physiology in salt and water balance. Gill morphology, biochemistry and molecular physiology were examined, with an emphasis on genes encoding TJ proteins. Fish were either fed a control or salt-enriched diet (~10 % NaCl) for 4 weeks prior to IPW exposure for 24 h. Serum [Na(+)], [Cl(-)] and muscle moisture content were unaltered by salt feeding, but changed in response to IPW irrespective of diet. Dietary salt loading altered the morphology (reduced Na(+)-K(+)-ATPase-immunoreactive cell numbers and surface exposure of mitochondrion-rich cells), biochemistry (decreased vacuolar-type H(+)-ATPase activity) and molecular physiology (decreased nkaα1a and cftrII mRNA abundance) of the gill in a manner indicative of reduced active ion uptake activity. But in control fish and not salt-fed fish, gill mRNA abundance of nkaα1c increased and nbc decreased after IPW exposure. Genes encoding TJ proteins were typically either responsive to salt feeding or IPW, but select genes responded to combined experimental treatment (e.g. IPW responsive but only if fish were salt-fed). Therefore, using salt feeding and IPW exposure, new insights into what factors influence gill TJ proteins and the role that specific TJ proteins might play in regulating the barrier properties of the gill epithelium have been acquired. In particular, evidence suggests that TJ proteins in the gill epithelium, or the regulatory networks that control them, respond independently to external or internal stimuli. PMID:27083431

  12. Complex polyion-surfactant ion salts in equilibrium with water: changing aggregate shape and size by adding oil.

    Science.gov (United States)

    Bernardes, Juliana S; Norrman, Jens; Piculell, Lennart; Loh, Watson

    2006-11-23

    The phase behavior of ternary mixtures containing an alkyltrimethylammonium polyacrylate complex salt, water, and a nonpolar "oil" (n-decanol, p-xylene or cyclohexane) is investigated. The complex salts were prepared with short or long polyacrylates (30 or 6000 repeating units) and with hexadecyltrimethylammonium or dodecyltrimethylammonium surfactant ions. Phase diagrams and structures were determined by visual inspection and small-angle X-ray scattering analyses. Systems containing decanol display a predominance of lamellar phases, while hexagonal phases prevail in systems containing p-xylene or cyclohexane. The difference is interpreted as a result of the different locations of the oils within the surfactant aggregates. Decanol is incorporated at the aggregate interface, leading to a decrease in its curvature, which favors the appearance of lamellar structures. p-Xylene and cyclohexane, on the other hand, are mostly incorporated in the interior of the cylindrical aggregate, as reflected by its swelling as the oil content increases. The comparison of these results with those reported for similar systems with monovalent (bromide) counterions indicates a much more limited swelling of the lamellar phases with polymeric counterions by water. This limited swelling behavior is predominantly ascribed to bridging due to the polyions. PMID:17107195

  13. Structure characterization and electrochemical properties of new lithium salt LiODFB for electrolyte of lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Lithium difluoro(axalato)borate (LiODFB) was synthesized in dimethyl carbonate (DMC) solvent and purified by the method of solventing-out crystallization.The structure characterization of the purified LiODFB was performed by Fourier transform infrared (FTIR) spectrometry and nuclear magnetic resonance (NMR) spectrometry.The electrochemical properties of the cells using I mol/L LiPF6 and 1 mol/L LiODFB in ethylene carbonate (EC)/DMC were investigated,respectively.The results indicate that LiODFB can be reduced at about 1.5 V and form a robust protective solid electrolyte interface (SEI) film on the graphite surface in the first cycle.The graphite/LiNi1/3Mn1/3Co1/3O2 cells with LiODFB-based electrolyte have very good capacity retention at 55 ℃,and show very good rate capability at 0.5C and 1C charge/discharge rate.Therefore,as a new salt,LiODFB is a most promising alternative lithium salt to replace LiPF6 for lithium ion battery electrolytes in the future.

  14. Calcium ion activity in physiological salt solutions: influence of anions substituted for chloride

    DEFF Research Database (Denmark)

    Christoffersen, Gert Rene Juul; Skibsted, Leif H

    1975-01-01

    1. Substitution by different anions for chloride in physiological salt solutions leads to binding between Ca2+ and the anion. Experiments designed to test effects of Cl- therefore often show mixed effects of changes in Cl- and Ca2+ activity.   2. This mixed effect is demonstrated in neurons...... of the snail, Helix pomatia: current-voltage characteristics and membrane potential are described during reduction of extracellular Cl- using different anions as substitutes. Methylsulphate is concluded to be the best substitute in this preparation. 3. The association constants for the binding of Ca2...

  15. Analysis of triazines and associated metabolites with electrospray ionization field-asymmetric ion mobility spectrometry/mass spectrometry

    DEFF Research Database (Denmark)

    Mie, Axel; Sandulescu, Madaline; Mathiasson, Lennart;

    2008-01-01

    Triazines comprise an important pollutant class owing to continued use in certain countries, and owing to strong environmental persistence that leads to problems even in countries like Sweden where the use of triazines has been prohibited for some years. We investigated mass-selective detection...... for ion sorting and discrimination against the considerable "chemical noise", nonspecific cluster and fragment ions, which are typically generated in electrospray ionization. This paper presents results of a pilot study of triazines and some metabolites in ideal solvents. Our long-range goal is automated...

  16. Interfacial behavior of perchlorate versus chloride ions in saturated aqueous salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Ghosal, S; Kuo, I W; Baer, M D; Bluhm, H

    2009-04-14

    In recent years combination of theoretical and experimental work have presented a novel view of the aqueous interface wherein hard and/or multiply charged ions are excluded from the interface, but large polarizable anions show interfacial enhancement relative to the bulk. The observed trend in the propensity of anions to adsorb at the air/water interface appears to be reverse of the Hofmeister series for anions. This study focuses on experimental and theoretical examination of the partitioning behavior of perchlorate (ClO{sub 4}{sup -}) and chloride (Cl{sup -}) ions at the air/water interface. We have used ambient pressure X-ray photoelectron spectroscopy technique to directly probe the interfacial concentrations of ClO{sub 4}{sup -} and Cl{sup -} ions in sodium perchlorate and sodium chloride solutions, respectively. Experimental observations are compared with first principles molecular dynamics simulations. Both experimental and simulation results show enhancement of ClO{sub 4}{sup -} ion at the interface, compared with the absence of such enhancement in the case of Cl{sup -} ion. These observations are in agreement with the expected trend in the interfacial propensity of anions based on the Hofmeister series.

  17. Molten salt synthesis of sodium lithium titanium oxide anode material for lithium ion batteries

    International Nuclear Information System (INIS)

    Highlights: • Na2Li2Ti6O12 has been successfully synthesized via a molten salt route. • Calcination temperature is an important effect on the component and microstructure of the product. • Pure phase Na2Li2Ti6O12 could be obtained at 700 °C for 2 h. - Abstract: The sodium lithium titanium oxide with composition Na2Li2Ti6O14 has been synthesized by a molten salt synthesis method using sodium chloride and potassium chloride mixture as a flux medium. Synthetic variables on the synthesis, such as sintering temperature, sintering time and the amount of lithium carbonate, were intensively investigated. Powder X-ray diffraction and scanning electron microscopy images of the reaction products indicates that pure phase sodium lithium titanium oxide has been obtained at 700 °C, and impure phase sodium hexatitanate with whiskers produced at higher temperature due to lithium evaporative losses. The results of cyclic voltammetry and discharge–charge tests demonstrate that the synthesized products prepared at various temperatures exhibited electrochemical diversities due to the difference of the components. And the sample obtained at 700 °C revealed highly reversible insertion and extraction of Li+ and displayed a single potential plateau at around 1.3 V. The product obtained at 700 °C for 2 h exhibits good cycling properties and retains the specific capacity of 62 mAh g−1 after 500 cycles

  18. Variation in viscosity and ion conductivity of a polymer–salt complex exposed to gamma irradiation

    Indian Academy of Sciences (India)

    Sujata Tarafdar; S K De; Sujit Manna; Udayan De; Pradyot Nanda

    2010-02-01

    We study changes in microstructure and resulting changes in the properties of PEO(1 − )–NH4 ClO4 () samples where = 0.18, when irradiated with gamma doses varying up to 50 kGy. Viscosities of aqueous solutions of the irradiated samples give an idea of the change in molecular weight and show correlation with ion conductivity. On the whole, there is a chain scission on irradiation, though there is evidence of some cross-linking at higher doses. The ion conductivity shows a strong increase for an irradiation of 35 kGy. DSC studies indicate a decrease in crystallinity with gamma dose.

  19. Interactive toxicity of major ion salts: Comparisons among species and between acute and chronic endpoints

    Science.gov (United States)

    Increased concentrations of major ions (Na, K, Ca, Mg, Cl, SO4, HCO3) in freshwater systems can result from a variety of anthropogenic activities, and can adversely affect aquatic organisms if the increase is sufficiently severe. Laboratory tests have indicated that the toxicity...

  20. Stable isotopes and major ion chemistry of continental salt lakes from southern Spain

    International Nuclear Information System (INIS)

    In several lakes from Southern of Spain, the parameters geochemical and isotopic (oxygen 18 and deuterium) have been studied. The main objective was establish the hydrological regimen by analysing the relationship between surface and groundwater in the different lakes using both isotopic and the hydrochemical characteristics of their waters and to quantify the degree of correlation between these variables. Lakes are systems that, although complex as is every natural system, are well fitted to the study of environmental isotopes. The origin and subsequent evaporative process of natural waters can be determined by the investigation of the relationship between the oxygen and hydrogen isotopes. A total of four lakes have been selected and according to the results obtained, the hydrological dynamics and the relation between salinity and isotopic content within the lakes studied could be determined. Two main hydrologic models have been established: a) Lakes with a mainly epigenetic hydrologic regime, in which very high isotopic contents are not found, seeing as, they have not had continuous evaporite processes, but instead have frequently dried up in summer (temporary lakes). In such systems a 'reflux brine' appears under the lake basin, and the brine magnitude is in proportion to the extension of the lake. It may be added that, even though the surface runoff is the main recharge component in the hydrologic cycle, these systems have some groundwater recharge when the piezometric levels are above the free water level and, so, they can store water even in low or zero precipitation periods in which, otherwise, they would dry up. In this way, an accurate classification would be epigenetic-mixed. b) Lakes in which the water shows several evaporite cycles. These kind of lakes do not have a very high salt content, but a very high isotopic content. They are permanent lakes in which the principal water balance component is groundwater. The classification is hypogenic, according

  1. Stable isotopes and major ion chemistry of continental salt lakes from Southern Spain

    International Nuclear Information System (INIS)

    Full text: In several lakes from Southern of Spain, the parameters geochemical and isotopic (δ18O and δ2H) have been studied. The main objective was establish the hydrological regimen by analysing the relationship between surface and groundwater in the different lakes using both isotopic and the hydrochemical characteristics of their waters and to quantify the degree of correlation between these variables. Lakes are systems that, although complex as is every natural system, are well fitted to the study of environmental isotopes. The origin and subsequent evaporative process of natural waters can be determined by the investigation of the relationship between the oxygen and hydrogen isotopes. A total of four lakes have been selected and according to the results obtained, the hydrological dynamics and the relation between salinity and isotopic content within the lakes studied could be determined. Two main hydrologic models have been established: a) Lakes with a mainly epigenetic hydrologic regime, in which very high isotopic contents are not found, seeing as, they have not had continuous evaporite processes, but instead have frequently dried up in summer (temporary lakes). In such systems a 'reflux brine' appears under the lake basin, and the brine magnitude is in proportion to the extension of the lake. It may be added that, even though the surface runoff is the main recharge component in the hydrologic cycle, these systems have some groundwater recharge when the piezometric levels are above the free water level and, so, they can store water even in low or zero precipitation periods in which, otherwise, they would dry up. In this way, an accurate classification would be epigenetic-mixed; b) Lakes in which the water shows several evaporite cycles. These kind of lakes do not have a very high salt content, but a very high isotopic content. They are permanent lakes in which the principal water balance component is groundwater. The classification is hypogenic, according

  2. Synthesis of rock-salt type lithium borohydride and its peculiar Li+ ion conduction properties

    Directory of Open Access Journals (Sweden)

    R. Miyazaki

    2014-05-01

    Full Text Available The high energy density and excellent cycle performance of lithium ion batteries makes them superior to all other secondary batteries and explains why they are widely used in portable devices. However, because organic liquid electrolytes have a higher operating voltage than aqueous solution, they are used in lithium ion batteries. This comes with the risk of fire due to their flammability. Solid electrolytes are being investigated to find an alternative to organic liquid. However, the nature of the solid-solid point contact at the interface between the electrolyte and electrode or between the electrolyte grains is such that high power density has proven difficult to attain. We develop a new method for the fabrication of a solid electrolyte using LiBH4, known for its super Li+ ion conduction without any grain boundary contribution. The modifications to the conduction pathway achieved by stabilizing the high pressure form of this material provided a new structure with some LiBH4, more suitable to the high rate condition. We synthesized the H.P. form of LiBH4 under ambient pressure by doping LiBH4 with the KI lattice by sintering. The formation of a KI - LiBH4 solid solution was confirmed both macroscopically and microscopically. The obtained sample was shown to be a pure Li+ conductor despite its small Li+ content. This conduction mechanism, where the light doping cation played a major role in ion conduction, was termed the “Parasitic Conduction Mechanism.” This mechanism made it possible to synthesize a new ion conductor and is expected to have enormous potential in the search for new battery materials.

  3. The role of ion pairs in the second-order NLO response of 4-X-1-methylpiridinium salts.

    Science.gov (United States)

    Tessore, Francesca; Cariati, Elena; Cariati, Franco; Roberto, Dominique; Ugo, Renato; Mussini, Patrizia; Zuccaccia, Cristiano; Macchioni, Alceo

    2010-02-01

    A series of 4-X-1-methylpyridinium cationic nonlinear optical (NLO) chromophores (X = (E)-CH=CHC(6)H(5); (E)-CH=CHC(6)H(4)-4'-C(CH(3))(3); (E)-CH=CHC(6)H(4)-4'-N(CH(3))(2); (E)-CH=CHC(6)H(4)-4'-N(C(4)H(9))(2); (E,E)-(CH=CH)(2)C(6)H(4)-4'-N(CH(3))(2)) with various organic (CF(3)SO(3)(-), p-CH(3)C(6)H(4)SO(3)(-)), inorganic (I(-), ClO(4)(-), SCN(-), [Hg(2)I(6)](2-)) and organometallic (cis-[Ir(CO)(2)I(2)](-)) counter anions are studied with the aim of investigating the role of ion pairing and of ionic dissociation or aggregation of ion pairs in controlling their second-order NLO response in anhydrous chloroform solution. The combined use of electronic absorption spectra, conductimetric measurements and pulsed field gradient spin echo (PGSE) NMR experiments show that the second-order NLO response, investigated by the electric-field-induced second harmonic generation (EFISH) technique, of the salts of the cationic NLO chromophores strongly depends upon the nature of the counter anion and concentration. The ion pairs are the major species at concentration around 10(-3) M, and their dipole moments were determined. Generally, below 5x10(-4) M, ion pairs start to dissociate into ions with parallel increase of the second-order NLO response, due to the increased concentration of purely cationic NLO chromophores with improved NLO response. At concentration higher than 10(-3) M, some multipolar aggregates, probably of H type, are formed, with parallel slight decrease of the second-order NLO response. Ion pairing is dependent upon the nature of the counter anion and on the electronic structure of the cationic NLO chromophore. It is very strong for the thiocyanate anion in particular and, albeit to a lesser extent, for the sulfonated anions. The latter show increased tendency to self-aggregate. PMID:20029883

  4. Molten salt synthesis of sodium lithium titanium oxide anode material for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yin, S.Y., E-mail: yshy2004@hotmail.com [College of Environmental and Biological Engineering, Wuhan Technology and Business University, Wuhan 430065 (China); Feng, C.Q. [Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for Synthesis and Applications of Organic Functional Molecules, Hubei University, Wuhan 430062 (China); Wu, S.J.; Liu, H.L.; Ke, B.Q. [College of Environmental and Biological Engineering, Wuhan Technology and Business University, Wuhan 430065 (China); Zhang, K.L. [College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072 (China); Chen, D.H. [College of Environmental and Biological Engineering, Wuhan Technology and Business University, Wuhan 430065 (China); Hubei Key Laboratory for Catalysis and Material Science, College of Chemistry and Material Science, South Central University for Nationalities, Wuhan 430074, Hubei (China)

    2015-09-05

    Highlights: • Na{sub 2}Li{sub 2}Ti{sub 6}O{sub 12} has been successfully synthesized via a molten salt route. • Calcination temperature is an important effect on the component and microstructure of the product. • Pure phase Na{sub 2}Li{sub 2}Ti{sub 6}O{sub 12} could be obtained at 700 °C for 2 h. - Abstract: The sodium lithium titanium oxide with composition Na{sub 2}Li{sub 2}Ti{sub 6}O{sub 14} has been synthesized by a molten salt synthesis method using sodium chloride and potassium chloride mixture as a flux medium. Synthetic variables on the synthesis, such as sintering temperature, sintering time and the amount of lithium carbonate, were intensively investigated. Powder X-ray diffraction and scanning electron microscopy images of the reaction products indicates that pure phase sodium lithium titanium oxide has been obtained at 700 °C, and impure phase sodium hexatitanate with whiskers produced at higher temperature due to lithium evaporative losses. The results of cyclic voltammetry and discharge–charge tests demonstrate that the synthesized products prepared at various temperatures exhibited electrochemical diversities due to the difference of the components. And the sample obtained at 700 °C revealed highly reversible insertion and extraction of Li{sup +} and displayed a single potential plateau at around 1.3 V. The product obtained at 700 °C for 2 h exhibits good cycling properties and retains the specific capacity of 62 mAh g{sup −1} after 500 cycles.

  5. Molecular model of a cell plasma membrane with an asymmetric multicomponent composition: Water permeation and ion effects

    Czech Academy of Sciences Publication Activity Database

    Vácha, Robert; Berkowitz, M. L.; Jungwirth, Pavel

    2009-01-01

    Roč. 96, č. 11 (2009), s. 4493-4501. ISSN 0006-3495 R&D Projects: GA ČR(CZ) GD203/05/H001; GA ČR GA203/08/0114 Grant ostatní: NSF(US) MCB-0615469 Institutional research plan: CEZ:AV0Z40550506 Keywords : membrane * ions * molecular dynamics Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.390, year: 2009

  6. Preparation of hybrid polymer based on polyurethane lithium salt and polyvinylidene fluoride as electrolyte for lithium-ion batteries

    International Nuclear Information System (INIS)

    Graphical abstract: The hybrid microporous membrane (PVDF/PLS-10) presents a uniform morphology and the corresponding HMGPE delivers high electrochemical stability and excellent cycleability. - Abstract: In this paper, hybrid microporous gel polymer electrolytes (HMGPEs) based onpolyvinylidene fluoride (PVdF)/polyurethane lithium salt (PLS) are fabricated by thermal phase separation technique. PLS is synthesized via condensation copolymerization of polyethylene glycol 800 (PEG800) and diphenyl-methane-diisocyanate(MDI), and then neutralized with LiOH. The effect of PLS on the morphologies of the hybrid membrane, electrochemical properties and cycle performance of the assembled polymer lithium-ion rechargeable batteries are studied in detail. The morphologies of the hybrid polymer membranes are examined by scanning electron microscope (SEM). The intercalation of PVdF/PLS hybrid membranes is characterized by X-ray diffraction (XRD), differential scanning calorimeter (DSC) and thermal gravimetric analysis (TGA). The incorporation of PLS in PVdF matrix can enhance ionic conductivities and electrochemical stabilities for the prepared HMGPEs. The assembled lithium-ion batteries based on HMGPEs with weight ratio 80:20 of PVdF and PLS (PVdF/PLS-20) delivers the highest charge-discharge capacity (about 175mAh g−1), and the cell based on HMGPEs of with weight ratio 90:10 of PVdF and PLS(PVdF/PLS-10) shows the best stability in cycle performance

  7. Electrochemical co-reduction between aluminium and lanthanide ions in fluoride salts: application to nuclear wastes pyrochemical treatment

    International Nuclear Information System (INIS)

    Nuclear reaction produces fission products such as lanthanides; these neutro-phage elements represent a poison for the nuclear chain reaction and have to be extracted. This thesis concerns lanthanides extraction (neodymium, cerium and samarium) by electrodeposition in the LiF-CaF2 eutectic mixture at 840 C. The process used is an alloy formation with aluminium by electrochemical co-reduction on an inert tungsten electrode. This technique is based on the simultaneous reduction of Al(III) and Ln(III) ions to obtain an alloy at the cathode. A decrease of the lanthanide activity in the alloy is obtained due to Al-Ln formation and a shift of lanthanide reduction potential to more positive values is observed: the theoretical extraction efficiency is then approaching 100 %. When both Ln(III) and Al(III) ions are present in the molten salt, new reduction waves appear between Al and Ln pure metal depositions and are attributed to Al-Ln alloy formation by co-reduction. The alloy compositions have been characterised in function of electrolysis potential: the more the electrolysis potential is negative, higher is the Ln content in the alloy. Finally, extractions by potentiostatic electrolyses have been carried out and the extraction efficiencies for the different lanthanides are higher than 99.4 %. (author)

  8. Stability diagrams for fourfold coordination of polyvalent metal ions in molten mixtures of halide salts

    International Nuclear Information System (INIS)

    The stability of local fourfold coordination for divalent and trivalent metal ions in liquid mixtures of polyvalent metal halides and alkali halides is classified by means of structural coordinates obtained from properties of the elements. In parallel with earlier classifications of compound crystal structures and molecular shapes, the elemental properties are taken from first-principles calculations of valence electron orbitals in atoms, in the form of (i) the nodal radii of Andreoni, Baldereschi and Guizzetti or (ii) the pseudopotential radii or Zunger and Cohen. As a third alternative a classification based on Pettifor's phenomenological chemical scale of the elements is also considered. The alternative structural classification schemes that are developed from these elemental properties are generally successfully in distinguishing molten mixtures in which the available experimental evidence indicates long-lived fourfold coordination of polyvalent metal ions. In addition, Pettifor's chemical scale scheme is useful in sorting out finer details of local coordination in the liquid state. 3 figs., 71 refs

  9. Effect of phytohormones on absorption and distribution of ions in salt-stressed bean plants

    Directory of Open Access Journals (Sweden)

    Zofia Starck

    2014-02-01

    Full Text Available Bean plant seedlings grown in water culture were treated for 5 days either with NaCl or with 7-times concentrated nutrient solution (diminished water potential by 3-103 hPa in both cases. Control and stressed plants were treated for 24 hrs with zeatin and GA,. NaCl-stress reduced distinctly ion absorption rate (K, Ca and P. Zeatin and GA3 promoted potassium uptake, but only in NaCI-treated plants. These hormones diminished Na accumulation in metabolically active organs but increased P- and Ca-content. In plants grown under both kind of stresses zeatin and GA3 partially reestablished the ratio of the main mono- to divalent cations, which increased in the leaves and apical part of the stressed plants. ABA introduced into the nutrient solution caused inhibition of the ion uptake (K, Ca, Mg and P. similar to that caused by NaCl-stress. The above reported results seem to confirm the supposition, that hormones act as an important factor contributing to regulation of both uptake and distribution of ions. In this way growth substances may also participate in the regulation of transport of various substances (among others - assimilates in the whole plant.

  10. 3-(Dicyanomethylidene)indan-1-one-Functionalized Calix[4]arene-Calix[4]pyrrole Hybrid: An Ion-Pair Sensor for Cesium Salts.

    Science.gov (United States)

    Yeon, Yerim; Leem, Soojung; Wagen, Corin; Lynch, Vincent M; Kim, Sung Kuk; Sessler, Jonathan L

    2016-09-01

    A chromogenic calix[4]arene-calix[4]pyrrole hybrid ion pair receptor bearing an indane substituent at a β-pyrrolic position has been prepared. On the basis of solution-phase UV-vis spectroscopic analysis and (1)H NMR spectroscopic studies carried out in 10% methanol in chloroform, receptor 1 is able to bind only cesium ion pairs (e.g., CsF, CsCl, and CsNO3) but not the constituent cesium cation (as its perchlorate salt) or the F(-), Cl(-), or NO3(-) anions (as the tetrabutylammonium salts). It thus displays rudimentary AND logic gate behavior. Receptor 1 shows a colorimetric response to cesium ion pairs under conditions of solid-liquid (nitrobenzene) and liquid-liquid (D2O-nitrobenzene-d5) extraction. PMID:27533478

  11. Change of electrostatic potential of mean force between two curved surfaces due to different salt composition, ion valence and size under certain ionic strength

    Science.gov (United States)

    Zhou, Shiqi

    2016-02-01

    Change of an electrostatic potential of mean force (EPMF) between two cylindrical rod surfaces with salt composition, ion valence, and ion size at a constant ionic strength of 0.3 M is studied by a classical density functional theory (CDFT) in a primitive model electrolyte solution. Several novel observations are made: (i) strength of a so-called like charge attraction (LCA) reduces in an invariable manner with the salt solution changing from single 2:1 electrolyte to mixture of 2:1 and 1:1 type electrolytes of varying concentration ratios; the change is even over entire range of the composition variation under low surface charge strength, and tends to be insensitive to the composition variation in the presence of the divalent counter-ion, and more and more drastic at a critical point the divalent counter-ion disappears, respectively, as the surface charge strength becomes big enough. (ii) Both monovalent counter-ion and co-ion diameters have only a marginal effect on both the LCA strength and equilibrium distance, and the former "abnormally" affects less than the latter. (iii) Depending on the surface charge strength considered, the divalent counter-ion diameter influences the LCA strength in solution comprised of 2:1 type and 1:1 type electrolytes, monotonously or non-monotonously. All of these findings provide forceful support for a recently proposed hydrogen-bonding style mechanism explaining the LCA.

  12. Increased abscisic acid levels in transgenic maize overexpressing AtLOS5 mediated root ion fluxes and leaf water status under salt stress.

    Science.gov (United States)

    Zhang, Juan; Yu, Haiyue; Zhang, Yushi; Wang, Yubing; Li, Maoying; Zhang, Jiachang; Duan, Liusheng; Zhang, Mingcai; Li, Zhaohu

    2016-03-01

    Abscisic acid (ABA) is a vital cellular signal in plants, and effective ABA signalling is pivotal for stress tolerance. AtLOS5 encoding molybdenum cofactor sulphurase is a key regulator of ABA biosynthesis. Here, transgenic AtLOS5 plants were generated to explore the role of AtLOS5 in salt tolerance in maize. AtLOS5 overexpression significantly up-regulated the expression of ZmVp14-2, ZmAO, and ZmMOCO, and increased aldehyde oxidase activities, which enhanced ABA accumulation in transgenic plants under salt stress. Concurrently, AtLOS5 overexpression induced the expression of ZmNHX1, ZmCBL4, and ZmCIPK16, and enhanced the root net Na(+) efflux and H(+) influx, but decreased net K(+) efflux, which maintained a high cytosolic K(+)/Na(+) ratio in transgenic plants under salt stress. However, amiloride or sodium orthovanadate could significantly elevate K(+) effluxes and decrease Na(+) efflux and H(+) influx in salt-treated transgenic roots, but the K(+) effluxes were inhibited by TEA, suggesting that ion fluxes regulated by AtLOS5 overexpression were possibly due to activation of Na(+)/H(+) antiport and K(+) channels across the plasma membrane. Moreover, AtLOS5 overexpression could up-regulate the transcripts of ZmPIP1:1, ZmPIP1:5, and ZmPIP2:4, and enhance root hydraulic conductivity. Thus transgenic plants had higher leaf water potential and turgor, which was correlated with greater biomass accumulation under salt stress. Thus AtLOS5 overexpression induced the expression of ABA biosynthetic genes to promote ABA accumulation, which activated ion transporter and PIP aquaporin gene expression to regulate root ion fluxes and water uptake, thus maintaining high cytosolic K(+) and Na(+) homeostasis and better water status in maize exposed to salt stress. PMID:26743432

  13. Ion contents, relative electrolyte leakage, proline accumulation, photosynthetic abilities and growth characters of oil palm seedlings in response to salt stress

    International Nuclear Information System (INIS)

    Oil palm seedlings were photo-autotrophically grown in MS medium and subsequently exposed to 0 (control), 25, 50, 100 or 200 mM NaCl. Sodium ions, proline content and the percentage of relative electrolyte leakage in seedlings subjected to salt stress increased, depending on the degree of salt concentrations. Sodium ion accumulation in oil palm seedlings grown under 200 mM NaCl was enriched and positively related to membrane injury or relative electrolyte leakage subsequently correlated with total chlorophyll degradation. Chlorophyll a (Chla), chlorophyll b (Chlb), total chlorophyll (TC), total carotenoids (Cx+c), maximum quantum yield of PSII (Fv/Fm), photon yield of PSII (OEPSII) and quantum efficiency of PSII (qP) in the seedlings under salt stress dropped significantly in comparison to the control group, leading to a reduction in net-photosynthetic rate (Pn) and growth, especially in 200 mM NaCl. A positive correlation between physiological and growth parameters, including sodium ion, relative electrolyte leakage, photosynthetic pigments and water oxidation in photosystem II, Pn and plant dry weight was found. These data may further be applied to establish criteria for salt tolerance screening in oil palm breeding programs. (author)

  14. A relationship between ion balance and the chemical compounds of salt inclusions found in the Greenland Ice Core Project and Dome Fuji ice cores

    DEFF Research Database (Denmark)

    Johnsen, Sigfus Johann; Dahl-Jensen, Dorthe; Steffensen, Jørgen Peder;

    2008-01-01

    on individual salt inclusions. The abundances in the ice cores are shown to reflect differences in climatic periods (the acidic environment of the Holocene versus the reductive environment of the last glacial maximum) and regional conditions (the marine environment of Antarctica versus the continental....... The dominant compounds depend only on the ion balance and the sequence of chemical reactions. In priority order, the principle salts are calcium sulfate, other sulfates, nitrate, chloride, and carbonate. The chemical abundances deduced by this method agree well with the results of Raman spectroscopy...

  15. Selective transport of ions and molecules across layer-by-layer assembled membranes of polyelectrolytes, p-sulfonato-calix[n]arenes and Prussian Blue-type complex salts.

    Science.gov (United States)

    Tieke, Bernd; Toutianoush, Ali; Jin, Wanqin

    2005-11-30

    Our recent studies in the field of ultrathin membranes prepared upon layer-by-layer assembly of various polyionic compounds such as polyelectrolytes, calixarenes and polyelectrolytes, and metal hexacyanoferrate salts such as Prussian Blue are reviewed. It is demonstrated that polyelectrolyte multilayers can be used (a) as nanofiltration and reverse osmosis membranes suitable for water softening and seawater desalination and (b) as molecular sieves and ion sieves for size-selective separation of neutral and charged aromatic compounds. Furthermore, hybrid membranes of p-sulfonato-calixarenes and cationic polyelectrolytes showing specific host-guest interactions with permeating ions are described. The membranes exhibit high selectivities for distinct metal ions. Finally, it is demonstrated that purely inorganic membranes of Prussian Blue (PB) and analogues can be prepared upon multiple sequential adsorption of transition metal cations and hexacyanoferrate anions. Due to the porous lattice of PB, the membranes are useful as ion filters able to separate cesium from sodium ions, for example. PMID:16091277

  16. Electrodialysis-ion exchange for the separation of dissolved salts. Final report

    International Nuclear Information System (INIS)

    The program described in this report studies the suitability of electrodialysis-ion exchange (EDIX) to treat aqueous streams containing heavy metals and radioactive cations in a solution containing sodium and nitrates. The goal of the program was to produce a cation stream containing sodium, heavy metals, and radioactive cations; an anion stream of nitric acid free of heavy metals and radioactive cations; and a product stream that meets discharge criteria. The experimental results, described in detail, indicated that EDIX was not a suitable process for treating wastes containing metals that formed insoluble hydroxides in a basic solution; the metals precipitate in the catholyte and feed compartments, and in the cathode membrane. The test program was therefore terminated prior to completion of all planned activities. 2 refs., 22 figs., 8 tabs

  17. Enhanced salt-removal percentage in capacitive deionization with addition of ion-exchange membrane using carbon electrode synthesized with freezing thawing method

    Science.gov (United States)

    Sari, Intan Permata; Endarko

    2016-04-01

    Ion-exchange membrane technology has shown a great potential to enhance the desalting efficiency. Ion-exchange membranes are placed in front of the electrodes so that the charged ions can be selectively passed through the membrane layer and captured by the oppositely charged electrode more quickly, so as to increase the efficiency of desalination. In this research, carbon electrodes have been synthesized from an activated carbon (700 - 1400 m2/g) and polyvinyl alcohol (PVA) as a binder using freezing thawing method. A solution with 180 µS/cm NaCl was pumped to the capacitive deionization (CDI) cell using a Boyu Submersible pump (model SP-601) at a flow rate of 25 mL/min and the voltage was set at 2 V. The result showed that the CDI cell with ion-exchange membrane (MCDI) has the salt removal efficiency greater than the CDI cell without ion-exchange membrane. The salt-removal percentage of MCDI was achieved at 66.36%, meanwhile the CDI cell without ion-exchange membrane resulted in 54.4%.

  18. A high sensitive ion pairing probe (the interaction of pyrenetetrasulphonate and methyl viologen): Salt and temperature dependences and applications

    International Nuclear Information System (INIS)

    The interaction between pyrenetetrasulphonate (PTS) and methyl viologen (MV2+) leads to a 1:1 charge transfer complex (CTC) in the concentration range below mmol L−1 of the ligands. Quantum mechanical calculations show the 1:1 complex having the planar moiety of PTS and the charges of the sulfonate groups stabilized by the twisted rings of the positively charged MV2+ species. The peculiar nature of PTS includes high fluorescence quantum yield (∼1), clear specular UV–vis spectra and fluorescence emission images, as well similar S2←S0 and S3←S0 transitions as those of S1←S0, all of them exhibiting well resolved vibrational structure. MV2+ has well known electron-accepting properties that favor the complexation. These features were studied as a function of salt concentration and temperature dependences allowing a detailed comprehension of static and dynamic association processes. Quantum mechanical calculations show the 1:1 stabilization of PTS/MV2+. In addition the effect of urea on the CTC equilibrium is presented, as expected the additive acts towards the non-complexed species (solvated free ions). The fluorescence quenching of MV2+over PTS highlights is one of the applications of this effect for giant vesicles characterization. - Highlights: • We determined the details of PTS/MV2+ 1:1 complex formation. • Ground and excited states formation is operative. • Ion pairing effects due to urea effect are shown. • Vesicle formation is illustrated by the pair

  19. Isotherms and Kinetics of Water Vapor Sorption/Desorption for Surface Films of Polyion-Surfactant Ion Complex Salts.

    Science.gov (United States)

    Gustavsson, Charlotte; Piculell, Lennart

    2016-07-14

    Thin films of "complex salts" (CS = ionic surfactants with polymeric counterions) have recently been shown to respond to humidity changes in ambient air by changing their liquid crystalline structure. We here report isotherms and kinetics of water sorption/desorption for ∼10-100 μm films of alkyltrimethylammonium polyacrylate CS, measured in a dynamic gravimetric vapor sorption instrument over a 0-95% relative humidity (RH) range. The sorption per ion pair was similar to that observed for common ionomers. A kinetic model for the water exchange is presented, assuming that the "external" transport between the vapor reservoir and the film surface is rate-determining. The model predicts that the water content, after a small stepwise change of the reservoir RH, should vary exponentially with time, with a time constant proportional to both the slope of the sorption isotherm and the film thickness. These predictions were confirmed for our films over large RH ranges, and the external mass transfer coefficient in our setup was calculated from the experimental data. Expressions derived for the Biot number (ratio of characteristic times for internal and external water transport) for the considered limiting case strongly indicate that external water transport should quite generally affect, or even dominate, the measured kinetics for similarly thin hydrated films. PMID:27327628

  20. Copper ion salts of arylthiotetrathiafulvalenes: synthesis, structure diversity and magnetic properties.

    Science.gov (United States)

    Ma, Longfei; Sun, Jibin; Lu, Xiaofeng; Zhang, Shangxi; Qi, Hui; Liu, Lei; Shao, Yongliang; Shao, Xiangfeng

    2015-01-01

    The combination of CuBr2 and arylthio-substituted tetrathiafulvalene derivatives (1-7) results in a series of charge-transfer (CT) complexes. Crystallographic studies indicate that the anions in the complexes, which are derived from CuBr2, show diverse configurations including linear [Cu(I)Br2](-), tetrahedral [Cu(II)Br4](2-), planar [Cu(II)2Br6](2-), and coexistence of planar [Cu(II)Br4](2-) and tetrahedral [Cu(II)Br3](-) ions. On the other hand, the TTFs show either radical cation or dication states that depend on their redox potentials. The central TTF framework on most of TTFs is nearly planar despite the charge on them, whereas the two dithiole rings on molecule 4 in complex 4·CuBr4 are significantly twisted with a dihedral angle of 38.3°. The magnetic properties of the complexes were elucidated. The temperature-dependent magnetic susceptibility of complex 5·Cu2Br6 shows the singlet-triplet transition with coupling constant J = -248 K, and that of 3·(CuBr4)0.5·CuBr3·THF shows the abrupt change at 270 K caused by the modulation of intermolecular interactions. The thermo variation of magnetic susceptibility for the other complexes follows the Curie-Weiss law, indicating the weak antiferromagnetic interaction at low temperature. PMID:26124886

  1. Salt-assisted liquid-liquid microextraction of Cr(VI) ion using an ionic liquid for preconcentration prior to its determination by flame atomic absorption spectrometry

    International Nuclear Information System (INIS)

    We report on the salt-assisted liquid-liquid microextraction of cationic complexes of Cr(VI) ion using the hydrophilic ionic liquid (IL) 1-butyl-3-methylimidazolium tetrafluoraborate and potassium hydrogen phosphate. This is a novel, simple, non-toxic and effective technique for sample pretreatment technique that displays large extraction efficiency and represents a new platform where Cr(VI) is complexed with 1,5-diphenylcarbazide (DPC) in sulfuric acid medium. It was applied to the extraction of Cr(VI) in the form of the Cr(VI)-DPC complex prior to its determination by flame atomic absorption spectrometry. Cr(III) ion also can be determined by this procedure after oxidation to Cr(VI). Extraction is mainly affected by the amount of water-soluble IL, the kind and quantity of inorganic salts, by pH and the concentration of DPC. Calibration plots are linear in the range from 3 to 150 μg L-1 of Cr(VI), and the limit of detection is 1. 25 μg L-1. The method was successfully applied to the speciation and determination of trace levels of Cr(III) and Cr(VI) in environmental water samples containing high levels of dissolved salts or food grade salts. (author)

  2. Investigation of the extraction equilibrium of ternary ion-association complexes of thallium(III) with monotetrazolium salts triphenyltetrazolium chloride and thiazolyl blue

    International Nuclear Information System (INIS)

    The extraction equilibrium of ternary ion-association complexes obtained during the reaction of tetrachloride complex of thallium(III) and monotetrazolium salts triphenyltetrazolium chloride (TTC) or thiazolyl blue (MTT) has been studied. The optimum conditions required for the investigations have been found. As a result of using a developed chemical model, the constants of extraction, distribution and association, the distribution coefficients and the recovery factor of the investigated ion-assocates have been determined radiochemically, by means of thallium 204 radiotracer technique. (author)

  3. PENENTUAN KADAR IODIDA DAN IODAT DALAM GARAM BERIODIUM DENGAN METODE KROMATOGRAFI CAIR KENERJA TINGGI PASANGAN ION [Determination of Iodate and Iodide Content in Iodized Salt By Ion Pair High Performance Liquid Chromatography Method

    Directory of Open Access Journals (Sweden)

    Wisnu Cahyadi1

    2004-04-01

    Full Text Available Two species of iodine, i.e. iodide and iodate in commercial iodized salt were determined using ion pair HPLC. From 15 samples analysed, the iodide and iodate content ranged from 24,05 ± 2,51 to 70,25 ± 3,78 ppm and from 31,43 ± 8,10 to 87,59 ± 0,44 ppm, respectively. The method used was found satisfactory in terms of precission, accuracy, sensitivity and selectivity, therefore the method seem acceptable for the determination of iodide and iodate content in iodized salt samples.

  4. Mechanism of dissolution of a lithium salt in an electrolytic solvent in a lithium ion secondary battery: a direct ab initio molecular dynamics (AIMD) study.

    Science.gov (United States)

    Tachikawa, Hiroto

    2014-06-01

    The mechanism of dissolution of the Li(+) ion in an electrolytic solvent is investigated by the direct ab initio molecular dynamics (AIMD) method. Lithium fluoroborate (Li(+)BF4(-)) and ethylene carbonate (EC) are examined as the origin of the Li(+) ion and the solvent molecule, respectively. This salt is widely utilized as the electrolyte in the lithium ion secondary battery. The binding of EC to the Li(+) moiety of the Li(+)BF4(-) salt is exothermic, and the binding energies at the CAM-B3LYP/6-311++G(d,p) level for n=1, 2, 3, and 4, where n is the number of EC molecules binding to the Li(+) ion, (EC)n(Li(+)BF4(-)), are calculated to be 91.5, 89.8, 87.2, and 84.0 kcal mol(-1) (per EC molecule), respectively. The intermolecular distances between Li(+) and the F atom of BF4(-) are elongated: 1.773 Å (n=0), 1.820 Å (n=1), 1.974 Å (n=2), 1.942 Å (n=3), and 4.156 Å (n=4). The atomic bond populations between Li(+) and the F atom for n=0, 1, 2, 3, and 4 are 0.202, 0.186, 0.150, 0.038, and 0.0, respectively. These results indicate that the interaction of Li(+) with BF4(-) becomes weaker as the number of EC molecules is increased. The direct AIMD calculation for n=4 shows that EC reacts spontaneously with (EC)3(Li(+)BF4(-)) and the Li(+) ion is stripped from the salt. The following substitution reaction takes place: EC+(EC)3(Li(+)BF4(-))→(EC)4Li(+)-(BF4(-)). The reaction mechanism is discussed on the basis of the theoretical results. PMID:24616076

  5. Determination of alkaline earth metal ions in solar salt by ion chromatography after solvent extraction with 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone

    International Nuclear Information System (INIS)

    Ion chromatography was effectively applied to the determination of alkaline earth elements (Mg, Ca, Sr and Ba) in solar salt after extraction with 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone (HPMBP) into MIBK. The recommended procedure was as follows : the samples (20 ∼ 50 g) were dissolved in about 150 ml of water and the solution was filtered through filter paper into a 200-ml volumetric flask. Ten ml of the sample was pipetted into a centrifuge tube, 5 ml of NH3-NH4Cl buffer solution (pH 9.5), and 15 ml 0.05 M HPMBP-MIBK solution were added. The mixture was shaken vigorously for 30 min. After the phases were separated, an 8-ml portion of the organic phase was transferred into another tube and the alkaline earth elements were back-extracted with 8 ml of the 0.1 M hydrochloric acid. The aqueous phase (6 ml) was heated on a hot plate at 100 deg C in order to remove the dissolved MIBK in the phase. After cooling to room temperature, the solution was diluted to 25 ml with water. A 100 μl aliquot of the sample was analyzed by use of an ion chromatograph (Yokogawa Hokushin Electric Works, model IC 100) equipped with a precolumn (PCX 1, 50 mm x 4.6 mm i.d.) and a separation column (SCX 1, 250 mm x 4.6 mm i.d.) by using 2 mM ethylene diamine-4 mM tartaric acid as a mobile phase (2 ml/min). The detection limits (S/N = 2) were 1.5 ppb for Mg2+, 3.4 ppb for Ca2+, 20 ppb for Sr2+ and 50 ppb for Ba2+, respectively. Relative standard deviation (n = 7) was less than 6.3 % for the simultaneous determination of four elements. The recoveries of Mg2+, Ca2+, Sr2+ and Ba2+ by the proposed method were 100 ∼ 105, 95 ∼ 105, 97 ∼ 101 and 95 ∼ 101 %, respectively. (author)

  6. Ion pairing with bile salts modulates intestinal permeability and contributes to food-drug interaction of BCS class III compound trospium chloride.

    Science.gov (United States)

    Heinen, Christian A; Reuss, Stefan; Amidon, Gordon L; Langguth, Peter

    2013-11-01

    In the current study the involvement of ion pair formation between bile salts and trospium chloride (TC), a positively charged Biopharmaceutical Classification System (BCS) class III substance, showing a decrease in bioavailability upon coadministration with food (negative food effect) was investigated. Isothermal titration calorimetry provided evidence of a reaction between TC and bile acids. An effect of ion pair formation on the apparent partition coefficient (APC) was examined using (3)H-trospium. The addition of bovine bile and bile extract porcine led to a significant increase of the APC. In vitro permeability studies of trospium were performed across Caco-2-monolayers and excised segments of rat jejunum in a modified Ussing chamber. The addition of bile acids led to an increase of trospium permeation across Caco-2-monolayers and rat excised segments by approximately a factor of 1.5. The addition of glycochenodeoxycholate (GCDC) was less effective than taurodeoxycholate (TDOC). In the presence of an olive oil emulsion, a complete extinction of the permeation increasing effects of bile salts was observed. Thus, although there are more bile acids in the intestine in the fed state compared to the fasted state, these are not able to form ion pairs with trospium in fed state, because they are involved in the emulsification of dietary fats. In conclusion, the formation of ion pairs between trospium and bile acids can partially explain its negative food effect. Our results are presumably transferable to other organic cations showing a negative food effect. PMID:23750707

  7. Evaluation and elimination of inhibitory effects of salts and heavy metal ions on biodegradation of Congo red by Pseudomonas sp. mutant.

    Science.gov (United States)

    Gopinath, Kannappan Panchamoorthy; Kathiravan, Mathur Natarajan; Srinivasan, Raman; Sankaranarayanan, Subramanian

    2011-02-01

    In this study, it was attempted to evaluate the influences and also recommended some elimination methods for inhibitory effects offered by salts and heavy metal ions. Congo red dye solution treated with mutant Pseudomonas sp. was taken as a model system for study. The salts used in this study are NaCl, CaCl(2) and MgSO(4)· 7H(2)O. Though the growth was inhibited at concentrations above 4 g/l, toleration was achieved by acclimatization process. In case of heavy metal ions, Cr (VI) showed low inhibition up to 500 mg/l of concentration, compared to Zn (II) and Cu (II). It was due to the presence of chromium reductase enzyme which was confirmed by SDS-PAGE. Zn (II) and Cu (II) ion inhibitions were eliminated by chelation with EDTA. The critical ion concentrations obtained as per Han-Levenspiel model for Cr (VI), Zn (II) and Cu (II) were 0.8958, 0.3028 and 0.204 g/l respectively. PMID:21177103

  8. Asymmetric collider

    International Nuclear Information System (INIS)

    The study of CP violation in beauty decay is one of the key challenges facing high energy physics. Much work has not yielded a definitive answer how this study might best be performed. However, one clear conclusion is that new accelerator facilities are needed. Proposals include experiments at asymmetric electron-positron colliders and in fixed-target and collider modes at LHC and SSC. Fixed-target and collider experiments at existing accelerators, while they might succeed in a first observation of the effect, will not be adequate to study it thoroughly. Giomataris has emphasized the potential of a new approach to the study of beauty CP violation: the asymmetric proton collider. Such a collider might be realized by the construction of a small storage ring intersecting an existing or soon-to-exist large synchrotron, or by arranging collisions between a large synchrotron and its injector. An experiment at such a collider can combine the advantages of fixed-target-like spectrometer geometry, facilitating triggering, particle identification and the instrumentation of a large acceptance, while the increased √s can provide a factor > 100 increase in beauty-production cross section compared to Tevatron or HERA fixed-target. Beams crossing at a non-zero angle can provide a small interaction region, permitting a first-level decay-vertex trigger to be implemented. To achieve large √s with a large Lorentz boost and high luminosity, the most favorable venue is the high-energy booster (HEB) at the SSC Laboratory, though the CERN SPS and Fermilab Tevatron are also worth considering

  9. Interpretation with a Donnan-based concept of the influence of simple salt concentration on the apparent binding of divalent ions to the polyelectrolytes polystyrenesulfonate and dextran sulfate

    Science.gov (United States)

    Marinsky, J.A.; Baldwin, Robert F.; Reddy, M.M.

    1985-01-01

    It has been shown that the apparent enhancement of divalent metal ion binding to polyions such as polystyrenesulfonate (PSS) and dextran sulfate (DS) by decreasing the ionic strength of these mixed counterion systems (M2+, M+, X-, polyion) can be anticipated with the Donnan-based model developed by one of us (J.A.M.). Ion-exchange distribution methods have been employed to measure the removal by the polyion of trace divalent metal ion from simple salt (NaClO4)-polyion (NaPSS) mixtures. These data and polyion interaction data published earlier by Mattai and Kwak for the mixed counterion systems MgCl2-LiCl-DS and MgCl2-CsCl-DS have been shown to be amenable to rather precise analysis by this model. ?? 1985 American Chemical Society.

  10. Ion-specific weak adsorption of salts and water/octanol transfer free energy of a model amphiphilic hexa-peptide

    International Nuclear Information System (INIS)

    An amphiphilic hexa-peptide has been used as a model to quantify how specific ion effects induced by addition of four salts tune the hydrophilic/hydrophobic balance and induce temperature-dependant coacervate formation from aqueous solution. The hexa-peptide chosen is present as a dimer with low transfer energy from water to octanol. Taking sodium chloride as the reference state in the Hofmeister scale, we identify water activity effects and therefore measure the free energy of transfer from water to octanol and separately the free energy associated to the adsorption of chaotropic ions or the desorption of kosmotropic ions for the same amphiphilic peptide. These effects have the same order of magnitude: therefore, both energies of solvation as well as transfer into octanol strongly depend on the nature of the electrolytes used to formulate any buffer. Model peptides could be used on separation processes based on criteria linked to 'Hofmeister' but different from volume and valency. (authors)

  11. Asymmetric interference in molecular photoprocesses

    International Nuclear Information System (INIS)

    For the first time, the Coulomb continuum effects in asymmetric molecular interference have been studied analytically in photoionization, photorecombination, bremsstrahlung and Compton ionization. Simple, closed-form factors describe the interference not only in monochromatic photoprocesses, but also in the continuous photoelectron spectra generated by attosecond x-ray pulses with a frequency-dependent phase and broad bandwidth. Using HeH2+ molecular ion as an example, we show how the plane wave interference pattern is strongly modified by the two-centre Coulomb continuum. Asymmetric Coulomb continuum introduces qualitative changes in a photoionization process

  12. Geometrical effect on the issue of asymmetric C 1s photoelectron angular distributions detected in coincidence with the fragment ion pairs of CO+–O+ for CO2 molecules

    International Nuclear Information System (INIS)

    We have measured C 1s photoelectron angular distributions (PADs) in coincidence with the CO+–O+ fragment ion pairs of CO2 molecules at the photoelectron energies of 85, 120 and 150 eV. The observed left–right asymmetric PADs have been well reproduced by our theoretical model taking into account the two degenerate zero-point bending vibrations. This leads to a conclusive result on the interpretation of such PADs; although it has been believed so far that they are the molecular frame, in fact they are the recoil frame. (fast track communications)

  13. Effectiveness of native and exotic arbuscular mycorrhizal fungi on nutrient uptake and ion homeostasis in salt-stressed Cajanus cajan L. (Millsp.) genotypes.

    Science.gov (United States)

    Garg, Neera; Pandey, Rekha

    2015-04-01

    Soil salinity is an increasing problem worldwide, restricting plant growth and production. Research findings show that arbuscular mycorrhizal (AM) fungi have the potential to reduce negative effects of salinity. However, plant growth responses to AM fungi vary as a result of genetic variation in mycorrhizal colonization and plant growth responsiveness. Thus, profitable use of AM requires selection of a suitable combination of host plant and fungal partner. A greenhouse experiment was conducted to compare effectiveness of a native AM fungal inoculum sourced from saline soil and two single exotic isolates, Funneliformis mossseae and Rhizophagus irregularis (single or dual mix), on Cajanus cajan (L.) Millsp. genotypes (Paras and Pusa 2002) under salt stress (0-100 mM NaCl). While salinity reduced plant biomass and disturbed ionic status in both genotypes, Pusa 2002 was more salt tolerant and ensured higher AM fungal colonization, plant biomass and nutrient content with favourable ion status under salinity. Although all AM fungi reduced negative effects of salt stress, R. irregularis (alone or in combination with F. mosseae) displayed highest efficiency under salinity, resulting in highest biomass, yield, nutrient uptake and improved membrane stability with favourable K(+)/Na(+) and Ca(2+)/Na(+) ratios in the host plant. Higher effectiveness of R. irregularis correlated with higher root colonization, indicating that the symbiosis formed by R. irregularis had more stable viability and efficiency under salt stress. These findings enhance understanding of the functional diversity of AM fungi in ameliorating plant salt stress tolerance and suggest the potential use of R. irregularis for increasing Cajanus cajan productivity in saline soils. PMID:25155616

  14. Mutation Breeding of Salt-tolerant and Ethanol-producing Strain S. cerevisiae H058 by Low-energy Ion Implantation

    Directory of Open Access Journals (Sweden)

    Shoubao Yan

    2014-07-01

    Full Text Available To obtain an industrial strain with high ethanol fermentation efficiency under salted conditions, the wild strain H058 of Saccharomyces cerevisiae was mutated by means of nitrogen ions implantation. Mutagenic effects of strain H058 by low energy N+ ion implantation were studied. A similar “saddle shape” survival curve due to ion beam irradiation appeared again in this study. By repeated screening, a high salt-tolerant and ethanol-producing strain M158 was obtained. Results showed that in medium contained 0, 1.5, 3.0, 4.5, 6.0% NaCl, M158 produced maximal ethanol of 98.3, 97.2, 96.4, 95.6 and 78.3 g/L at 54, 54, 54 and 72 h, respectively. However, the original strain H058 maximal ethanol of 95.2, 90.9, 84.8, 79.4 and 67.5 g/L at 60, 60, 66 and 72 h, respectively. In addition, the ethanol yield (g/g in all of the NaCl concentrations for M158 is 0.492, 0.486, 0.482, 0.48 and 0.392 g/g, respectively, which were higher than those (0.476, 0.455, 0.424, 0.397 and 0.338 g/g, respectively of the original strain H058. The higher production and shorter fermentation period suggest that strain M158 is a good salt-tolerant and ethanol-producing strain.

  15. Application of normal pulse voltammetric technique for on-line monitoring of lanthanide ions in LiCl-KCl molten salt at 773K

    International Nuclear Information System (INIS)

    The applicability of normal pulse voltammetry (NPV) to on-line monitoring of lanthanide ions in a molten salt system has been investigated for use in the pyrochemical process. It was revealed from NPV curves for lanthanides that the limiting currents for lanthanides linearly increased at lanthanide concentration of less than 2.5 wt%. However, it was observed that the concentration dependence of the limiting currents was not linear at higher concentration. It is thought from those results that NPV could be considered as a promising way to monitor concentration of lanthanides in the pyrochgemical process if the concentration range of analytes is properly controlled. (author)

  16. Phase behavior of polyion-surfactant ion complex salts: effects of surfactant chain length and polyion length.

    Science.gov (United States)

    Svensson, Anna; Norrman, Jens; Piculell, Lennart

    2006-06-01

    The aqueous phase behavior of a series of complex salts, containing cationic surfactants with polymeric counterions, has been investigated by visual inspection and small-angle X-ray scattering (SAXS). The salts were alkyltrimethylammonium polyacrylates, CxTAPAy, based on all combinations of five surfactant chain lengths (C6, C8, C10, C12, and C16) and two lengths of the polyacrylate chain (30 and 6 000 repeating units). At low water contents, all complex salts except C6TAPA6000 formed hexagonal and/or cubic Pm3n phases, with the hexagonal phase being favored by lower water contents. The aggregate dimensions in the liquid crystalline phases changed with the surfactant chain length. The determined micellar aggregation numbers of the cubic phases indicated that the micelles were only slightly aspherical. At high water contents, the C6TAPAy salts were miscible with water, whereas the other complex salts featured wide miscibility gaps with a concentrated phase in equilibrium with a (sometimes very) dilute aqueous solution. Thus, the attraction between oppositely charged surfactant aggregates and polyions decreases with decreasing surfactant chain length, and with decreasing polyion length, resulting in an increased miscibility with water. The complex salt with the longest surfactant chains and polyions gave the widest miscibility gap, with a concentrated hexagonal phase in equilibrium with almost pure water. A decrease in the attraction led to cubic-micellar and micellar-micellar coexistence in the miscibility gap and to an increasing concentration of the complex salt in the dilute phase. For each polyion length, the mixtures for the various surfactant chain lengths were found to conform to a global phase diagram, where the surfactant chain length played the role of an interaction parameter. PMID:16722736

  17. Hydronium-dominated ion transport in carbon-dioxide-saturated electrolytes at low salt concentrations in nanochannels

    DEFF Research Database (Denmark)

    Lund Jensen, Kristian; Kristensen, Jesper Toft; Crumrine, Andrew Michael;

    2011-01-01

    Nanochannel ion transport is known to be governed by surface charge at low ionic concentrations. In this paper, we show that this surface charge is typically dominated by hydronium ions arising from dissolution of ambient atmospheric carbon dioxide. Taking the hydronium ions into account, we model...

  18. Simultaneous analysis of silicon and boron dissolved in water by combination of electrodialytic salt removal and ion-exclusion chromatography with corona charged aerosol detection.

    Science.gov (United States)

    Mori, Masanobu; Sagara, Katsuya; Arai, Kaori; Nakatani, Nobutake; Ohira, Shin-Ichi; Toda, Kei; Itabashi, Hideyuki; Kozaki, Daisuke; Sugo, Yumi; Watanabe, Shigeki; Ishioka, Noriko S; Tanaka, Kazuhiko

    2016-01-29

    Selective separation and sensitive detection of dissolved silicon and boron (DSi and DB) in aqueous solution was achieved by combining an electrodialytic ion isolation device (EID) as a salt remover, an ion-exclusion chromatography (IEC) column, and a corona charged aerosol detector (CCAD) in sequence. DSi and DB were separated by IEC on the H(+)-form of a cation exchange resin column using pure water eluent. DSi and DB were detected after IEC separation by the CCAD with much greater sensitivity than by conductimetric detection. The five-channel EID, which consisted of anion and cation acceptors, cathode and anode isolators, and a sample channel, removed salt from the sample prior to the IEC-CCAD. DSi and DB were scarcely attracted to the anion accepter in the EID and passed almost quantitatively through the sample channel. Thus, the coupled EID-IEC-CCAD device can isolate DSi and DB from artificial seawater and hot spring water by efficiently removing high concentrations of Cl(-) and SO4(2-) (e.g., 98% and 80% at 0.10molL(-1) each, respectively). The detection limits at a signal-to-noise ratio of 3 were 0.52μmolL(-1) for DSi and 7.1μmolL(-1) for DB. The relative standard deviations (RSD, n=5) of peak areas were 0.12% for DSi and 4.3% for DB. PMID:26755416

  19. SEI Formation and Interfacial Stability of a Si Electrode in a LiTDI-Salt Based Electrolyte with FEC and VC Additives for Li-Ion Batteries.

    Science.gov (United States)

    Lindgren, Fredrik; Xu, Chao; Niedzicki, Leszek; Marcinek, Marek; Gustafsson, Torbjörn; Björefors, Fredrik; Edström, Kristina; Younesi, Reza

    2016-06-22

    An electrolyte based on the new salt, lithium 4,5-dicyano-2-(trifluoromethyl)imidazolide (LiTDI), is evaluated in combination with nano-Si composite electrodes for potential use in Li-ion batteries. The additives fluoroethylene carbonate (FEC) and vinylene carbonate (VC) are also added to the electrolyte to enable an efficient SEI formation. By employing hard X-ray photoelectron spectroscopy (HAXPES), the SEI formation and the development of the active material is probed during the first 100 cycles. With this electrolyte formulation, the Si electrode can cycle at 1200 mAh g(-1) for more than 100 cycles at a coulombic efficiency of 99%. With extended cycling, a decrease in Si particle size is observed as well as an increase in silicon oxide amount. As opposed to LiPF6 based electrolytes, this electrolyte or its decomposition products has no side reactions with the active Si material. The present results further acknowledge the positive effects of SEI forming additives. It is suggested that polycarbonates and a high LiF content are favorable components in the SEI over other kinds of carbonates formed by ethylene carbonate (EC) and dimethyl carbonate (DMC) decomposition. This work thus confirms that LiTDI in combination with the investigated additives is a promising salt for Si electrodes in future Li-ion batteries. PMID:27220376

  20. Characterization of Ion Contents and Metabolic Responses to Salt Stress of Different Arabidopsis AtHKT1;1 Genotypes and Their Parental Strains

    Institute of Scientific and Technical Information of China (English)

    Camilla B.Hill; Deepa Jha; Antony Bacic; Mark Tester; Ute Roessner

    2013-01-01

    Plants employ several strategies to maintain cellular ion homeostasis under salinity stress,including mediating ion fluxes by transmembrane transport proteins and adjusting osmotic pressure by accumulating osmolytes.The HKT (high-affinity potassium transporter) gene family comprises Na+ and Na+/K+ transporters in diverse plant species,with HKT1;1 as the only member in Arabidopsis thaliana.Cell-type-specific overexpression of AtHKT1;1 has been shown to prevent shoot Na+ overaccumulation under salinity stress.Here,we analyzed a broad range of metabolites and elements in shoots and roots of different AtHKT1;1 genotypes and their parental strains before and after salinity stress,revealing a reciprocal relationship of metabolite differences between an AtHKT1;1 knockout line (hktl;1) and the AtHKT1;1 overexpressing lines (E2586 UASGAL4:HKT1;1 and J2731*UASGAL4:HKT1;1).Although levels of root sugars were increased after salt stress in both AtHKT1;1 overexpressing lines,E2586 UASGAL4:HKT1;1 showed higher accumulation of the osmoprotectants trehalose,gentiobiose,and melibiose,whereas J2731*UASGAL4:HKT1;1 showed higher levels of sucrose and raffinose,compared with their parental lines,respectively.In contrast,the knockout line hktl;1 showed strong increases in the levels of the tricarboxylic acid (TCA) cycle intermediates in the shoots after salt treatment.This coincided with a significant depletion of sugars,suggesting that there is an increased rate of carbon influx into the TCA cycle at a constant rate of C-efflux from the cycle,which might be needed to support plant survival during salt stress.Using correlation analysis,we identified associations between the Na+ content and several sugars,suggesting that regulation of sugar metabolism is important in plant responses to salinity stress.

  1. Lorentz Force on Sodium and Chlorine Ions in a Salt Water Solution Flow under a Transverse Magnetic Field

    Science.gov (United States)

    De Luca, R.

    2009-01-01

    It is shown that, by applying elementary concepts in electromagnetism and electrochemistry to a system consisting of salt water flowing in a thin rectangular pipe at an average velocity v[subscript A] under the influence of a transverse magnetic field B[subscript 0], an electromotive force generator can be conceived. In fact, the Lorentz force…

  2. Hydronium-dominated ion transport in carbon-dioxide-saturated electrolytes at low salt concentrations in nanochannels

    DEFF Research Database (Denmark)

    Pennathur, Sumita; Kristensen, Jesper; Crumrine, Andrew;

    2011-01-01

    Nanochannel ion transport is known to be governed by surface charge at low ionic concentrations. In this talk, we show that this surface charge is dominated by hydronium ions arising from dissolution of ambient atmospheric carbon dioxide. By refining the electrokinetic model of the nanochannel...

  3. Asymmetric Ashes

    Science.gov (United States)

    2006-11-01

    that oscillate in certain directions. Reflection or scattering of light favours certain orientations of the electric and magnetic fields over others. This is why polarising sunglasses can filter out the glint of sunlight reflected off a pond. When light scatters through the expanding debris of a supernova, it retains information about the orientation of the scattering layers. If the supernova is spherically symmetric, all orientations will be present equally and will average out, so there will be no net polarisation. If, however, the gas shell is not round, a slight net polarisation will be imprinted on the light. This is what broad-band polarimetry can accomplish. If additional spectral information is available ('spectro-polarimetry'), one can determine whether the asymmetry is in the continuum light or in some spectral lines. In the case of the Type Ia supernovae, the astronomers found that the continuum polarisation is very small so that the overall shape of the explosion is crudely spherical. But the much larger polarization in strongly blue-shifted spectral lines evidences the presence, in the outer regions, of fast moving clumps with peculiar chemical composition. "Our study reveals that explosions of Type Ia supernovae are really three-dimensional phenomena," says Dietrich Baade. "The outer regions of the blast cloud is asymmetric, with different materials found in 'clumps', while the inner regions are smooth." "This study was possible because polarimetry could unfold its full strength thanks to the light-collecting power of the Very Large Telescope and the very precise calibration of the FORS instrument," he adds. The research team first spotted this asymmetry in 2003, as part of the same observational campaign (ESO PR 23/03 and ESO PR Photo 26/05). The new, more extensive results show that the degree of polarisation and, hence, the asphericity, correlates with the intrinsic brightness of the explosion. The brighter the supernova, the smoother, or less clumpy

  4. THz Spectroscopic Investigation of Energetic Ion Salt%含能离子盐的太赫兹光谱研究

    Institute of Scientific and Technical Information of China (English)

    黄平; 邱睿

    2012-01-01

    In order to further explore the terahertz spectrum characteristics of energetic ion salts on the basis of the research on traditional nitro energetic materials, and extend applicable scope of terahertz wave technology in the study of safety testing field, experimental measurement and theoretical analysis of THz spectrum for new energetic ion salts (5-ATN and BMDATHBT) were introduced. The absorption coefficient of the samples was measured in the region of 0. 5 ~ 2. 0 THz by time-domain spectroscopy and by Fourier transform infrared spectroscopy in the 2. 0~8. 0 THz region. Using the density functional theory methods, the vibration characteristics were simulated by Gaussian 03 and Materials Studio 4. 3. The simulated spectrum of samples is in agreement with the experimental data. The result showed that ion salts have the typical absorption peaks that have close relation with the tribal structure, and the interaction between particles and the single skeleton vibrations of individual ion are the main reason for energetic ion salt to form absorption peak in terahertz band, which provides references for detecting high nitrogen compounds by terahertz technique.%在传统硝基含能材料研究的基础上,进一步探索含能离子盐类物质的太赫兹波谱特性,拓宽太赫兹波技术在安全检测领域的应用研究范围,对新型含能离子盐(5-ATN,BMDATHBT)进行了太赫兹时域光谱和傅里叶变换红外光谱的实验测量,得到样品在0.5~8.0 THz范围内的吸收频谱.基于密度泛函理论,采用Gaussian 03及Materials Studio 4.3量子化学软件分别进行单分子与晶胞形式的模拟计算,结果与实验值较为一致.研究发现,含能离子盐5-ATN,BMDATHBT具有明显的特征吸收峰,这与此类物质的结构有密切关系,离子间的相互作用及单个离子的骨架振动是离子型化合物在太赫兹频段形成吸收峰的主要原因.研究为利用太赫兹波技术检测高氮离子型化合物提供了参考.

  5. Intermolecular, ion-molecular and interionic interactions in solutions of lithium and tetrabutylammonium salts in mixtures of methanol with propylene carbonate

    International Nuclear Information System (INIS)

    Interparticle interactions are investigated in solutions of LiI, LiBr, LiCl, LiNCS, (C4H9)4NI, (C4H9)4NBr, (C4H9)4NCl in mixtures of methanol with propylene carbonate in absence of self-association of molecules of methanol and in different salt concentrations by the methods of IR spectroscopy. Intermolecular and ion-molecular interactions are studied on IR absorption lines of valent vibrations of OH-groups of methanol (3300-3500 cm-1), interionic interaction - on lines of valent CN (2000-2100 cm-1) and deformation O-Cl-O (625 cm-1) vibrations of NVS- and ClO4- correspondingly. Concentrations of lithium complexes forming in solutions are calculated on intensities of valent absorption lines of OH-groups of methanol. In the case of salt concentration increase the content of complexes decreases. Ousting of solvent molecule by anions in complex happens so faster as electron-donor ability of it is higher

  6. Temperature dependence of corrosion inhibition of steels used in oil well stimulation using acetylenic compound and halide ion salt mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Menezes, M.A.M. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Escola de Quimica], E-mail: marcom@eq.ufrj.br; Valle, M.L.M. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Escola de Quimica. Dept. de Processos Organicos; Dweck, J. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Escola de Quimica. Dept. de Processos Inorganicos; Queiroz Neto, J.C. [Petroleo Brasileiro S.A. (CENPES / PETROBRAS), Rio de Janeiro, RJ (Brazil). Centro de Pesquisas

    2007-07-15

    Halogenated salt (HS)-acetylenic compound (AC) mixtures were tested as corrosion inhibitors of 13Cr and 22Cr stainless steel and N80 and P110 carbon steel when exposed to 15 wt.% HCl solutions, at 50 deg C, 80 deg C and 100 deg C. The best corrosion inhibition efficiency is obtained when the concentration of both AC and HS is 1.5 wt. %, which indicates the use of all tested steels in oil well stimulation operated at 50 deg C and the use of 13Cr, N80 and P110 steels in oil well processing temperatures up to 100 deg C. (author)

  7. Electrodeposited tin coating as negative electrode material for lithium-ion battery in room temperature molten salt

    OpenAIRE

    Fung, YS; Zhu, DR

    2002-01-01

    A new room temperature molten salt (RTMS) [1-methyl-3-ethylimidazolium/AlCl3/SnCl2 (3:2:0.5)] was developed for depositing tin on a copper electrode. Different tin crystallites were deposited at different temperatures, giving widely different performances of the assembled lithium cell [Sn (Cu)/LiCl buffered MEICl-AlCl3 RTMS/lithium]. Tin film deposited at 50°C or higher gave a more desirable crystal structure and an improved performance than films obtained at lower temperatures. Both cyclic v...

  8. In situ synthesis of ultra-fine, porous, tin oxide-carbon nanocomposites via a molten salt method for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Bin [Institute of Applied Chemistry, Xinjiang University, Urumqi 830046 (China); School of Science, Xinjiang Eduction Institute, Urumqi, Xinjiang (China); Guo, Zai Ping [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); Institute of Applied Chemistry, Xinjiang University, Urumqi 830046 (China); School of Mechanical, Materials and Mechatronics Engineering, University of Wollongong, NSW 2522 (Australia); Du, Guodong; Hassan, Mohd Faiz [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); School of Mechanical, Materials and Mechatronics Engineering, University of Wollongong, NSW 2522 (Australia); Nuli, Yanna [Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); School of Mechanical, Materials and Mechatronics Engineering, University of Wollongong, NSW 2522 (Australia); Jia, Dianzeng [Institute of Applied Chemistry, Xinjiang University, Urumqi 830046 (China); School of Mechanical, Materials and Mechatronics Engineering, University of Wollongong, NSW 2522 (Australia)

    2010-08-15

    Ultra-fine, porous, tin oxide-carbon (SnO{sub 2}/C) nanocomposites are fabricated by a molten salt method at 300 C, and malic acid is decomposed as the carbon source. In situ synthesis is favourable for the combination of carbon and SnO{sub 2}. The structure and morphology are confirmed by X-ray diffraction analysis, specific surface-area measurements, and transmission electron microscopy (TEM). Examination of TEM images reveals that the SnO{sub 2} nanoparticles are embedded in the carbon matrix, with sizes between 2 and 5 nm. The electrochemical measurements show that the nanocomposite delivers a high capacity with good capacity retention as an anode material for lithium-ion batteries, due to the combination of the ultra-fine porous structure and the carbon component. (author)

  9. Salt Bridge Rearrangement (SaBRe) Explains the Dissociation Behavior of Noncovalent Complexes

    Science.gov (United States)

    Loo, Rachel R. Ogorzalek; Loo, Joseph A.

    2016-04-01

    Native electrospray ionization-mass spectrometry, with gas-phase activation and solution compositions that partially release subcomplexes, can elucidate topologies of macromolecular assemblies. That so much complexity can be preserved in gas-phase assemblies is remarkable, although a long-standing conundrum has been the differences between their gas- and solution-phase decompositions. Collision-induced dissociation of multimeric noncovalent complexes typically distributes products asymmetrically (i.e., by ejecting a single subunit bearing a large percentage of the excess charge). That unexpected behavior has been rationalized as one subunit "unfolding" to depart with more charge. We present an alternative explanation based on heterolytic ion-pair scission and rearrangement, a mechanism that inherently partitions charge asymmetrically. Excessive barriers to dissociation are circumvented in this manner, when local charge rearrangements access a lower-barrier surface. An implication of this ion pair consideration is that stability differences between high- and low-charge state ions usually attributed to Coulomb repulsion may, alternatively, be conveyed by attractive forces from ion pairs (salt bridges) stabilizing low-charge state ions. Should the number of ion pairs be roughly inversely related to charge, symmetric dissociations would be favored from highly charged complexes, as observed. Correlations between a gas-phase protein's size and charge reflect the quantity of restraining ion pairs. Collisionally-facilitated salt bridge rearrangement (SaBRe) may explain unusual size "contractions" seen for some activated, low charge state complexes. That some low-charged multimers preferentially cleave covalent bonds or shed small ions to disrupting noncovalent associations is also explained by greater ion pairing in low charge state complexes.

  10. Salt Tolerance in Soybean

    Institute of Scientific and Technical Information of China (English)

    Tsui-Hung Phang; Guihua Shao; Hon-Ming Lam

    2008-01-01

    Soybean is an Important cash crop and its productivity is significantly hampered by salt stress. High salt Imposes negative impacts on growth, nodulation, agronomy traits, seed quality and quantity, and thus reduces the yield of soybean. To cope with salt stress, soybean has developed several tolerance mechanisms, including: (I) maintenance of ion homeostasis; (ii) adjustment in response to osmotic stress; (iii) restoration of osmotic balance; and (iv) other metabolic and structural adaptations. The regulatory network for abiotic stress responses in higher plants has been studied extensively in model plants such as Arabidopsis thaliana. Some homologous components involved in salt stress responses have been identified in soybean. In this review, we tried to integrate the relevant works on soybean and proposes a working model to descdbe Its salt stress responses at the molecular level.

  11. Novel chiral N4S2- and N6S3-donor macrocyclic ligands: synthesis, protonation constants, metal-ion binding and asymmetric catalysis in the Henry reaction.

    Science.gov (United States)

    Gao, Jian; Martell, A E

    2003-08-01

    New hydrophobic chiral macrocyclic ligands L1-L3 with chiral diamino and thiophene moieties have been synthesized by the Schiff base condensation approach. Protonation constants of L1 and L2 were determined by potentiometry titration. Metal-ion binding experiments exhibited that L1 and L3 are pronounced in selective recognition, Ag+, Cu2+ and Ca2+ ions among the surveyed metal ions (Cu2+, Co2+, Ni2+, Zn2+, Cd2+, Pb2+, Ag+, Li+, Na+, K+, and Ca2+). L1 was found to spectroscopically detect the presence of Cu2+ and Ca2+ to function as a multiple readout sensor. The detection limit for Ca2+ ions was found to be 9.8 x 10(-5) M in CH2Cl2-MeOH solution. The trimeric chiral ligand L3 has been shown to be an efficient auxiliary in a Zn(II)-mediated enantioselective Henry reaction. PMID:12948208

  12. Effects of solvents and salt on the thermal stability of lithiated graphite used in lithium ion battery.

    Science.gov (United States)

    Wang, Qingsong; Sun, Jinhua; Chen, Chunhua

    2009-08-15

    The thermal stability of lithiated graphite in the presence of solvents, electrolytes and LiPF(6) salt was studied using C80 micro-calorimeter. The presence of cyclic carbonates or linear carbonates increases the activity of Li(x)C(6)-solvent coexisting system, especially for the Li(x)C(6)-linear carbonates one. LiPF(6) was detected that it increases the activity greatly of its coexisting system with lithiated graphite. The coexisting system of Li(x)C(6) with the electrolyte of LiPF(6)/ethylene carbonate+diethyl carbonate shows less thermal stability, which is attributed to the activity between diethyl carbonate and Li(x)C(6). This also agrees with the experiment result of Li(x)C(6)-diethyl carbonate coexisting system. PMID:19261386

  13. Time- and Space-Resolved SAXS Experiments Inform on Phase Transition Kinetics in Hydrated, Liquid-Crystalline Films of Polyion-Surfactant Ion "Complex Salts".

    Science.gov (United States)

    Li, Joaquim; Gustavsson, Charlotte; Piculell, Lennart

    2016-05-24

    Detailed time- and space-resolved SAXS experiments show the variation with hydration of liquid crystalline structures in ethanol-cast 5-80 μm thick films of polyion-surfactant ion "complex salts" (CS). The CS were dodecyl- (C12) or hexadecyl- (C16) trimethylammonium surfactants with polyacrylate (DP 25 or 6000) counter-polyions. The experiments were carried out on vertical films in humid air above a movable water bath, so that gradients of hydration were generated, which could rapidly be altered. Scans over different positions along a film, kept fixed relative to the bath, showed that the surfactant aggregates of the various liquid-crystalline CS structures grow in cross-sectional area with decreasing hydration. This behavior is attributed to the low water content. Studies of films undergoing rapid dehydration, made possible by the original experimental setup, gave strong evidence that some of the investigated systems remain kinetically trapped for minutes in a nonequilibrium Pm3n micellar cubic phase before switching to the equilibrium P6mm 2D hexagonal phase. Both the length of the polyion and the length of the surfactant hydrocarbon "tail" affect the kinetics of the phase transition. The slowness of the cubic-to-hexagonal structural transition is attributed to the fact that it requires major rearrangements of the polyions and surfactant ions relative to each other. By contrast, other structure changes, such as between the hexagonal and rectangular phases, were observed to occur much more rapidly. PMID:27153140

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

    Directory of Open Access Journals (Sweden)

    Divarova Vidka V.

    2015-01-01

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

  15. Extraction-Spectrophotometric Method for Determination of Gallium(III) in the Form of Ion Associate with a Monotetrazolium Salt

    Science.gov (United States)

    Stojnova, K. T.; Divarov, V. V.; Racheva, P. V.; Lekova, V. D.

    2015-11-01

    The possibility of application of the ternary ion-association complex of gallium(III), 4-(2-pyridyl azo)resorcinol (PAR) and 2,3,5-triphenyl-2H-tetrazolium chloride (TTC) for extraction-spectrophotometric determination of gallium(III) was studied. The liquid-liquid extraction system Ga(III)-PAR-TTC-H2O-CHCl3 was applied for this purpose. The effect of the foreign ions on the extraction was investigated. Based on the obtained results, a sensitive, relatively simple, and inexpensive method for determination of gallium(III) in a model mixture was developed, which can be implemented in industrial, biological, medical, and pharmaceutical samples.

  16. Asymmetric Wettability Directs Leidenfrost Droplets

    Energy Technology Data Exchange (ETDEWEB)

    Agapov, Rebecca L [ORNL; Boreyko, Jonathan B [ORNL; Briggs, Dayrl P [ORNL; Srijanto, Bernadeta R [ORNL; Retterer, Scott T [ORNL; Collier, Pat [ORNL; Lavrik, Nickolay V [ORNL

    2014-01-01

    Leidenfrost phenomena on nano- and microstructured surfaces are of great importance for increasing control over heat transfer in high power density systems utilizing boiling phenomena. They also provide an elegant means to direct droplet motion in a variety of recently emerging fluidic systems. Here, we report the fabrication and characterization of tilted nanopillar arrays (TNPAs) that exhibit directional Leidenfrost water droplets under dynamic conditions, namely on impact with Weber numbers 40 at T 325 C. The batch fabrication of the TNPAs was achieved by glancing-angle anisotropic reactive ion etching of a thermally dewet platinum mask, with mean pillar diameters of 100 nm and heights of 200-500 nm. In contrast to previously implemented macro- and microscopic Leidenfrost ratchets, our TNPAs induce no preferential directional movement of Leidenfrost droplets under conditions approaching steady-state film boiling, suggesting that the observed droplet directionality is not a result of asymmetric vapor flow. Using high-speed imaging, phase diagrams were constructed for the boiling behavior upon impact for droplets falling onto TNPAs, straight nanopillar arrays, and smooth silicon surfaces. The asymmetric impact and directional trajectory of droplets was exclusive to the TNPAs for impacts corresponding to the transition boiling regime, revealing that asymmetric wettability upon impact is the mechanism for the droplet directionality.

  17. Electrochemical characteristics of Li 2- xVTiO 4 rock salt phase in Li-ion batteries

    Science.gov (United States)

    Dominko, R.; Garrido, C. Vidal-Abraca; Bele, M.; Kuezma, M.; Arcon, I.; Gaberscek, M.

    Li 2- xVTiO 4/C sample with a disordered rock salt structure was successfully prepared by annealing at a temperature of 850 °C. The electrochemical oxidation in the first cycle occurs at voltages above 4 V vs. metallic lithium, while the shapes of the electrochemical curves in consequent reduction-oxidation processes show a monotonous change of the potential between the selected cut-off voltages. A linear combination fit of individual XANES spectra was used for the determination of the oxidation states of as prepared sample and intermediate states during oxidation and reduction. In the as-prepared sample, vanadium was found to be in the average oxidation state of V 3.5+ and was additionally oxidized to V 3.8+ by the electrochemical charging. During the discharge process, the vanadium oxidation state was reduced to V 3.0+. In situ X-ray diffraction patterns and EXAFS analysis suggest good structural stability during oxidation and reduction, which is also reflected in the cycling stability if batteries were cycled in the voltage window between 2.0 V and 4.4 V. Extension of the lower cut-off voltage to 1.0 V doubles the capacity retention with the improved capacity stability if compared with several high capacity vanadium based materials.

  18. Anion- interactions in layered structures of salts of 5-(hydroxyimino) quinolin-8-one and related salts

    Indian Academy of Sciences (India)

    Prithiviraj Khakhlary; Jubaraj B Baruah

    2015-01-01

    Relevance of anion- interactions in chloride, bromide, nitrate and perchlorate salts of 5-(hydroxyimino)quinolin-8-one are discussed. Structures of nitrate salt of 5-aminoquinoline as well as nitrate salt of 4-hydroxyquinazoline are compared with the structure of nitrate salt of 5-(hydroxyimino)quinolin-8-one. From such a comparison, two different arrangements of nitrate ions with respect to the respective cations are discerned. Nitrate ions are sandwiched between aromatic planes of cations in nitrate salts of 5-(hydroxyimino)quinolin-8-one or 4-hydroxyquinazoline; whereas, nitrate ions are in oblique positions with respect to aromatic planes of counter cations in nitrate salt of 5-aminoquinoline. Binding constants of different nitrate salts in solution are determined by UV-visible spectroscopic titrations. Solution study shows formation of ion-pairs of these salts in solution.

  19. Anion Partitioning and Ion-Pairing Behavior of Anions in the Extraction of Cesium Salts by 4,5'-bix(tert-octylbenzo)dibenzo-24-crown-8 in 1,2-Dichloroethane

    International Nuclear Information System (INIS)

    A systematic study of anion partitioning and ion-pairing was performed for an extraction of individual cesium salts into 1,2-dichloroethane (1,2-DCE) using 4,5(doubleprime)-bis(tert-octylbenzo)dibenzo-24-crown-8 as the cesium receptor. Equilibrium constants corresponding to the extraction of ion pairs and dissociated ions, formation of the 1:1 cesium/crown complex (confirmed by electrospray mass spectrometry), and dissociation of the ion pairs in water-saturated 1,2-DCE at 25 C were obtained from equilibrium modeling using the SXLSQI program. The standard Gibbs energy of partitioning between water and water-saturated 1,2-DCE was determined for picrate, permanganate, trifluoromethanesulfonate, methanesulfonate, trifluoroacetate, and acetate anions. The dissociation of the organic-phase complex ion pair [Cs(4,4(doubleprime)-bis(tert-octylbenzo)dibenzo-24-crown-8)]+NO3 observed in the extraction experiments was shown to be consistent with the dissociation constant determined independently by conductance measurements. As attributed to the large effective radius of the complex cation, the evident anion discrimination due to ion-pairing in the 1,2-DCE phase, was relatively small, by comparison only a tenth of the discrimination exhibited by the anion partitioning. Only chloride and picrate exhibit evidence for significantly greater-than-expected ion-pairing tendency. These results provide insight into the inclusion properties of the clefts formed by opposing arene rings of the crown ether upon encapsulation of the Cs+ ion, whose weak anion recognition likely reflects the preferential inclusion of 1,2-DCE molecules in the clefts. Observed anion extraction selectivity in this system, which may be ascribed predominantly to solvent-induced Hofmeister bias selectivity toward large charge-diffuse anions, was nearly the same whether cesium salts were extracted as dissociated ions or ion pairs

  20. Determination of the electrochemical performance and stability of the lithium-salt, lithium 4,5-dicyano-2-(trifluoromethyl) imidazolide, with various anodes in Li-ion cells

    Science.gov (United States)

    Paillet, Sabrina; Schmidt, Gregory; Ladouceur, Sébastien; Fréchette, Joël; Barray, Francis; Clément, Daniel; Hovington, Pierre; Guerfi, Abdelbast; Vijh, Ashok; Cayrefourcq, Ian; Zaghib, Karim

    2015-12-01

    The electrochemical performance and stability of lithium 4,5-dicyano-2-(trifluoromethyl) imidazolide (LiTDI), which is a promising lithium salt for electrolytes in lithium-ion batteries, are discussed. The power capability of LiTDI in EC/DEC (3/7 v/v) in half cells was evaluated with standard anodes used in the lithium-ion battery industry: graphite and Li4Ti5O12 (LTO). The effects of two additives, vinylene carbonate (VC) and fluoro-ethylene carbonate (FEC), were investigated (2% weight in EC/DEC) and compared with a reference electrolyte, 1 M LiPF6 (EC/DEC + 2%VC). LiTDI forms a thin SEI with FEC that is uniformly deposited on graphite, which allows high power capability with 93.9% of the specific capacity at 10C (92.3% for 1 M LiPF6 + 2%VC). Excellent results were also obtained for LiTDI with LTO, 91.1% of the specific capacity was recovered at 10C vs. 91.5% for LiPF6. The stability of LiTDI was evaluated in pouch-cells: LFP/LTO (1C-rate) and NMC/LTO (C/4-rate). The results show that the performance of LiTDI is comparable to that of LiPF6, 85.4% of the capacity was recovered after 900 cycles (87.6% for LiPF6) for LFP/LTO, and 85.8% of capacity was obtained after 450 cycles (86.3% for LiPF6) for NMC/LTO.

  1. Extraction-spectrophotometric study of ternary ion-association complexes of vanadium (4) with pyrogallol and tetrazolium salts

    International Nuclear Information System (INIS)

    The systems V(4)-pyrogallol-neotetrazolium chloride and V(4)-pyrogallo-iodonitrotetrazolium chloride are studied using spectrophotometric methods. The composition of the complexes is established. Obtained results reveal that the ternary ion-association complexes are easily extracted by butanol. The optimum conditions for extraction of vanadium into n-butanol are found. Distribution constants, recovery factors, association constants and molar absorptivities ε are calculated. Molar absorptivity of the ternary complex with 2-(4-iodophenyl)-3-(4-nitrophenyl)-tetrazolium chloride (ε=8.74·103 l/mol·cm) is higher as compared to that of the complex with 2,2';5,5'-tetraphenyl-3,3'-(p-biphenyl)-ditetrazolium chloride (ε=7.30·103 l/mol·cm) and to molar absorptivities of the ternary complexes with antipyrine (ε=4.2·103 l/mol·cm) and diphenylguanidine (ε=8.0·103 l/mol·cm)

  2. Chapter 6. Uranium extraction possibilities from natural uranium-bearing waters of complex salt composition. 6.2. Technology for uranium extraction from brine with a high content of ion-chlorine

    International Nuclear Information System (INIS)

    Present article is devoted to technology for uranium extraction from brine with a high content of ion-chlorine. The content of basic anions and cations in lake waters of Sasik-Kul deposit was defined. Results of X-ray spectral analysis of salt residual after water evaporation from Sasik-Kul lake was discussed. Investigations revealed that uranium extraction from brines containing ion-chlorine is possible. The developed basic process flow diagram of uranium extraction from Sasik-Kul Lake' brine consists of the following basic stages: evaporation, leaching, catching of formed gases (HCl), sorption, desorption, deposition, drying and tempering.

  3. 土壤盐胁迫降低后甜高粱的补偿生长和盐离子分布特征%The compensation growth and salt ion distribution in sweet sorghum (Sorghum bicolor L. Moench) after salt stress reduction

    Institute of Scientific and Technical Information of China (English)

    李春宏; 郭文琦; 张培通; 殷剑美; 韩晓勇; 王立

    2016-01-01

    Adversity compensation effect is ubiquity in crops, which impacts on crop growth, development and yield. To elucidate the compensation growth of sweet sorghum following soil salt stress reduction, a pot experiment was conducted, in which 5 g×kg-1 (high salt), 2 g×kg-1 down from 5 g×kg-1 (salt stress reduction) and 2 g×kg-1 (low-salt control) of soil salt treatments were applied at the elongation stage of sweet sorghum. Then growth rate of dry matter on aboveground parts (leaf, leaf sheath and stem) and aboveground dry matter at maturity of two cultivated sweet sorghum varieties were determined. The experiment also measured salt ions (K+, Na+ and Cl-) distribution in aboveground organs of sweet sorghum. The results showed that the growth rate of aboveground dry matter in high salt treatment was always significantly lower than that of control. There was clear acceleration of growth after soil salt reduction, and gradually exceeded the growth of control due to overcompensation effect. At maturity stage, both plant height and aboveground dry matter of two sorghum varieties decreased sharply in high salt treatment. They decreased by 7.69% and 33.21%, respectively, in ‘Liaotian 1’ in salt stress reduction treatment compared with the low-salt control, moreover, no obviously difference was found in both plant height and aboveground dry matter of ‘Zhongketian 3’ between salt stress reduction treatment and low-salt control. The contents of Na+and Cl-in aboveground organs significantly increased, and K+content slightly increased under high salt stressed condition. At 35 days after soil salt reduction, the contents of Na+ and Cl- still higher than that of low-salt control, but decreased significantly compared to that of high salt treatment. Although K+content in both leaf sheath and stem in soil salt reduction treatment were higher than that of low-salt control, no difference was observed in leaf. The results suggested that ion toxicity in salt-stressed sweet

  4. The Asymmetric Leximin Solution

    OpenAIRE

    Driesen, Bram W.

    2012-01-01

    In this article we define and characterize a class of asymmetric leximin solutions, that contains both the symmetric leximin solution of Imai[5] and the two-person asymmetric Kalai-Smorodinsky solution of Dubra [3] as special cases. Solutions in this class combine three attractive features: they are defined on the entire domain of convex n-person bargaining problems, they generally yield Pareto efficient solution outcomes, and asymmetries among bargainers are captured by a single parameter ve...

  5. Asymmetric WIMP dark matter

    OpenAIRE

    Graesser, Michael L.; Shoemaker, Ian M.; Vecchi, Luca

    2011-01-01

    In existing dark matter models with global symmetries the relic abundance of dark matter is either equal to that of anti-dark matter (thermal WIMP), or vastly larger, with essentially no remaining anti-dark matter (asymmetric dark matter). By exploring the consequences of a primordial asymmetry on the coupled dark matter and anti-dark matter Boltzmann equations we find large regions of parameter space that interpolate between these two extremes. Interestingly, this new asymmetric WIMP framewo...

  6. A Semi-Analytical Line Transfer (SALT) model to interpret the spectra of galaxy outflows

    CERN Document Server

    Scarlata, C

    2015-01-01

    We present a Semi-Analytical Line Transfer model, SALT, to study the absorption and re-emission line profiles from expanding galactic envelopes. The envelopes are described as a superposition of shells with density and velocity varying with the distance from the center. We adopt the Sobolev approximation to describe the interaction between the photons escaping from each shell and the remaining of the envelope. We include the effect of multiple scatterings within each shell, properly accounting for the atomic structure of the scattering ions. We also account for the effect of a finite circular aperture on actual observations. For equal geometries and density distributions, our models reproduce the main features of the profiles generated with more complicated transfer codes. Also, our SALT line profiles nicely reproduce the typical asymmetric resonant absorption line profiles observed in star-forming/starburst galaxies whereas these absorption profiles cannot be reproduced with thin shells moving at a fixed out...

  7. Synthesis, Characterization and Properties of Asymmetric Methide Anion Based Ionic Liquids Containing Nitrile Groups

    Institute of Scientific and Technical Information of China (English)

    ZOU Ting; LU Liang; LIU Xiu-Li; ZHANG Zhan; WANG Li-Bing; FU Xian-Lei; GAO Guo-Hua; KOU Yuan; HE Ming-Yuan

    2008-01-01

    A series of asymmetric methide anion based ionic liquids containing nitrile groups have been synthesized for the first time using the method of ion-exchange between sodium/potassium methide and various quaternary bro-mide/chloride salts of trimethylamine, triethylamine, tributylamine, N-methylpyrrolidine, and N-methylimidazole. All of the functionalised ionic liquids were characterized by IR, 1H, 13C NMR, MS and elemental analysis. The de-composition temperature of the ionic liquids measured via TGA ranged from 219 to 339 ℃. The functionalised ionic liquid, [Bmim][C(CN)2COCH3], was used as a ligand for Suzuki coupling reaction. The yields of the coupling reaction increased 10%-15% by the addition of the functionalised ionic liquid, [Bmim] [C(CN)2COCH3].

  8. Crystal structures of five 1-alkyl-4-aryl-1,2,4-triazol-1-ium halide salts

    Directory of Open Access Journals (Sweden)

    Marites A. Guino-o

    2015-06-01

    Full Text Available The asymmetric units for the salts 4-(4-fluorophenyl-1-isopropyl-1,2,4-triazol-1-ium iodide, C11H13FN3+·I−, (1, 1-isopropyl-4-(4-methylphenyl-1,2,4-triazol-1-ium iodide, C12H16N3+·I−, (2, 1-isopropyl-4-phenyl-1,2,4-triazol-1-ium iodide, C11H14N3+·I−, (3, and 1-methyl-4-phenyl-1,2,4-triazol-1-ium iodide, C9H10N3+·I−, (4, contain one cation and one iodide ion, whereas in 1-benzyl-4-phenyl-1,2,4-triazol-1-ium bromide monohydrate, C15H14N3+·Br−·H2O, (5, there is an additional single water molecule. There is a predominant C—H...X(halide interaction for all salts, resulting in a two-dimensional extended sheet network between the triazolium cation and the halide ions. For salts with para-substitution on the aryl ring, there is an additional π–anion interaction between a triazolium carbon and iodide displayed by the layers. For salts without the para-substitution on the aryl ring, the π–π interactions are between the triazolium and aryl rings. The melting points of these salts agree with the predicted substituent inductive effects.

  9. Modeling on sensitivity of soil salt ions to electrical conductivity of soil extract%土壤盐分离子对浸提液电导率的敏感性分析建模

    Institute of Scientific and Technical Information of China (English)

    马亮; 何继武; 刘锋; 陈亮亮

    2011-01-01

    A study was conducted on the sensitivity of soil salt ions to the electrical conductivity of soil extract to promote technical progress in improved alkaline field and salt-water movement theory in depth. A preliminary qualitative analysis was first made by applying grey relational analysis in electrical conductivity of soil extract and salt ions, and then by default factor analysis and principal component analysis for further authentication. The results show that: Cl ~ and Na+ ions are mors sensitive than any other ions to the electrical conductivity of soil extract; the results of gray relational analysis method are the same as the results of principal component analysis model based on the default factor method; the seven salt ions have multicollinearity on electrical conductivity of soil extract, and the conductivity prediction model based on principal component regression method can make reasonable simulation of variables. This provides a new way for further study on salt - water movement theory.%为了研究土壤盐分离子对浸提液电导率的敏感性,首先采用灰色关联分析法对影响土壤浸提液电导率的盐分离子进行初步分析,之后采用缺省因子法与主成分分析法进一步分析检验.结果表明:Cl-、Na+这两种离子对土壤浸提液电导率的变化最为敏感;灰色关联分析法所得结果与基于缺省因子法的主成分分析模型结果基本一致;影响土壤浸提液电导率的7种盐分离子之间存在多重共线性,应用主成分回归方法建立的电导率预测模型能够对实测变量作出合理的模拟.

  10. Novel binary deep eutectic electrolytes for rechargeable Li-ion batteries based on mixtures of alkyl sulfonamides and lithium perfluoroalkylsulfonimide salts

    Science.gov (United States)

    Geiculescu, O. E.; DesMarteau, D. D.; Creager, S. E.; Haik, O.; Hirshberg, D.; Shilina, Y.; Zinigrad, E.; Levi, M. D.; Aurbach, D.; Halalay, I. C.

    2016-03-01

    Ionic liquids (IL's) were proposed for use in Li-ion batteries (LIBs), in order to mitigate some of the well-known drawbacks of LiPF6/mixed organic carbonates solutions. However, their large cations seriously decrease lithium transference numbers and block lithium insertion sites at electrode-electrolyte interfaces, leading to poor LIB rate performance. Deep eutectic electrolytes (DEEs) (which share some of the advantages of ILs but possess only one cation, Li+), were then proposed, in order to overcome the difficulties associated with ILs. We report herein on the preparation, thermal properties (melting, crystallization, and glass transition temperatures), transport properties (specific conductivity and viscosity) and thermal stability of binary DEEs based on mixtures of lithium bis(trifluoromethane)sulfonimide or lithium bis(fluoro)sulfonimide salts with an alkyl sulfonamide solvent. Promise for LIB applications is demonstrated by chronoamperometry on Al current collectors, and cycling behavior of negative and positive electrodes. Residual current densities of 12 and 45 nA cm-2 were observed at 5 V vs. Li/Li+ on aluminum, 1.5 and 16 nA cm-2 at 4.5 V vs. Li/Li+, respectively for LiFSI and LiTFSI based DEEs. Capacities of 220, 130, and 175 mAh· g-1 were observed at low (C/13 or C/10) rates, respectively for petroleum coke, LiMn1/3Ni1/3Co1/3O2 (a.k.a. NMC 111) and LiAl0.05Co0.15Ni0.8O2 (a.k.a. NCA).

  11. Asymmetric Wettability Directs Leidenfrost Droplets

    Science.gov (United States)

    Agapov, Rebecca; Boreyko, Jonathan; Briggs, Dayrl; Srijanto, Bernadeta; Retterer, Scott; Collier, C. Patrick; Lavrik, Nickolay

    2014-03-01

    Exploration of Leidenfrost droplets on nano- and microstructured surfaces are of great importance for increasing control over heat transfer in high power density systems using boiling phenomena. They also provide an elegant way to direct droplet motion in a variety of emerging fluidic systems. Here, we report the fabrication and characterization of tilted nanopillar arrays (TNPAs) that exhibit directional Leidenfrost water droplets under dynamic conditions. The batch fabrication of the TNPAs was achieved by glancing-angle anisotropic reactive ion etching of a thermally dewet platinum mask. In contrast to previously implemented macro- and microscopic Leidenfrost ratchets, our TNPAs induce no preferential directional movement of Leidenfrost droplets under conditions approaching steady-state film boiling. This suggests that the observed droplet directionality is not a result of asymmetric vapor flow. Phase diagrams were constructed for the boiling behavior upon droplet impact onto TNPAs, straight nanopillar arrays, and smooth silicon surfaces. Asymmetric wettability and directional trajectory of droplets was exclusive to the TNPAs for impacts corresponding to the transition boiling regime, revealing this to be the mechanism for the droplet directionality. This work was conducted at the Center for Nanophase Materials Sciences, which is sponsored at Oak Ridge National Lab by the Division of Scientific User Facilities, US Dept. of Energy.

  12. Asymmetric Magnetic Reconnection in Weakly Ionized Chromospheric Plasmas

    CERN Document Server

    Murphy, Nicholas A

    2015-01-01

    Realistic models of magnetic reconnection in the solar chromosphere must take into account that the plasma is partially ionized and that plasma conditions within any two magnetic flux bundles undergoing reconnection may not be the same. Asymmetric reconnection in the chromosphere may occur when newly emerged flux interacts with pre-existing, overlying flux. We present 2.5D simulations of asymmetric reconnection in weakly ionized, reacting plasmas where the magnetic field strengths, ion and neutral densities, and temperatures are different in each upstream region. The plasma and neutral components are evolved separately to allow non-equilibrium ionization. As in previous simulations of chromospheric reconnection, the current sheet thins to the scale of the neutral-ion mean free path and the ion and neutral outflows are strongly coupled. However, the ion and neutral inflows are asymmetrically decoupled. In cases with magnetic asymmetry, a net flow of neutrals through the current sheet from the weak field (high ...

  13. Synthesis and characterization of a new family of aryl-trifluoromethanesulfonylimide Li-Salts for Li-ion batteries and beyond

    Science.gov (United States)

    Ladouceur, Sébastien; Paillet, Sabrina; Vijh, Ashok; Guerfi, Abdelbast; Dontigny, Martin; Zaghib, Karim

    2015-10-01

    The battery energy-storage industry is evolving rapidly so new battery components are needed with high stability and improved energy density, as well as enhanced safety. In this paper, results on new salts, safer degradation and good electrochemical performances are reported. Four organic anions for Li-salts were synthesized and their conductivity, viscosity and electrochemical potential window in EC/DEC (3/7) solutions were examined. These salts have high thermal stability and safer degradation products (compared to LiPF6 and Li-TFSI), which were identified by TGA-MS. Cyclic voltammetry measurements showed their electrochemical window and oxidation limits were at least 4.3 and 4.5 V vs Li/Li+ using a platinum and high surface area carbon material working electrode, respectively. The salts passivated the common aluminum current collector at 4.4 V vs Li/Li+ and without corrosion. The properties of one Li salts were evaluated in half cell configuration as a model system using lithium iron phosphate (LFP), lithium titanate oxide (LTO) and graphite as electrodes. The performance of the salt showed promising behavior in the model system, compared to benchmark salts such as LiPF6 and Li-TFSI.

  14. Thomson scattering measurements from asymmetric interpenetrating plasma flows

    International Nuclear Information System (INIS)

    Imaging Thomson scattering measurements of collective ion-acoustic fluctuations have been utilized to determine ion temperature and density from laser produced counter-streaming asymmetric flows. Two foils are heated with 8 laser beams each, 500 J per beam, at the Omega Laser facility. Measurements are made 4 mm from the foil surface using a 60 J 2ω probe laser with a 200 ps pulse length. Measuring the electron density and temperature from the electron-plasma fluctuations constrains the fit of the multi-ion species, asymmetric flows theoretical form factor for the ion feature such that the ion temperatures, ion densities, and flow velocities for each plasma flow are determined

  15. Thomson scattering measurements from asymmetric interpenetrating plasma flows

    Energy Technology Data Exchange (ETDEWEB)

    Ross, J. S., E-mail: ross36@llnl.gov; Moody, J. D.; Fiuza, F.; Ryutov, D.; Divol, L.; Huntington, C. M.; Park, H.-S. [Lawrence Livermore National Laboratory, P.O. Box 808, Livermore, California 94551 (United States)

    2014-11-15

    Imaging Thomson scattering measurements of collective ion-acoustic fluctuations have been utilized to determine ion temperature and density from laser produced counter-streaming asymmetric flows. Two foils are heated with 8 laser beams each, 500 J per beam, at the Omega Laser facility. Measurements are made 4 mm from the foil surface using a 60 J 2ω probe laser with a 200 ps pulse length. Measuring the electron density and temperature from the electron-plasma fluctuations constrains the fit of the multi-ion species, asymmetric flows theoretical form factor for the ion feature such that the ion temperatures, ion densities, and flow velocities for each plasma flow are determined.

  16. Phosphate salts

    Science.gov (United States)

    ... levels that are too high, and for preventing kidney stones. They are also taken for treating osteomalacia (often ... But intravenous phosphate salts should not be used. Kidney stones (nephrolithiasis). Taking potassium phosphate by mouth might help ...

  17. Salt cookbook

    CERN Document Server

    Saha, Anirban

    2015-01-01

    If you are a professional associated with system and infrastructure management, looking at automated infrastructure and deployments, then this book is for you. No prior experience of Salt is required.

  18. Asymmetric reactions in continuous flow

    Directory of Open Access Journals (Sweden)

    Xiao Yin Mak

    2009-04-01

    Full Text Available An overview of asymmetric synthesis in continuous flow and microreactors is presented in this review. Applications of homogeneous and heterogeneous asymmetric catalysis as well as biocatalysis in flow are discussed.

  19. Salt splitting with ceramic membranes

    Energy Technology Data Exchange (ETDEWEB)

    Kurath, D. [Pacific Northwest National Lab., Richland, WA (United States)

    1996-10-01

    The purpose of this task is to develop ceramic membrane technologies for salt splitting of radioactively contaminated sodium salt solutions. This technology has the potential to reduce the low-level waste (LLW) disposal volume, the pH and sodium hydroxide content for subsequent processing steps, the sodium content of interstitial liquid in high-level waste (HLW) sludges, and provide sodium hydroxide free of aluminum for recycle within processing plants at the DOE complex. Potential deployment sites include Hanford, Savannah River, and Idaho National Engineering Laboratory (INEL). The technical approach consists of electrochemical separation of sodium ions from the salt solution using sodium (Na) Super Ion Conductors (NaSICON). As the name implies, sodium ions are transported rapidly through these ceramic crystals even at room temperatures.

  20. Ion Colliders

    CERN Document Server

    Fischer, W

    2014-01-01

    High-energy ion colliders are large research tools in nuclear physics to study the Quark-Gluon-Plasma (QGP). The range of collision energy and high luminosity are important design and operational considerations. The experiments also expect flexibility with frequent changes in the collision energy, detector fields, and ion species. Ion species range from protons, including polarized protons in RHIC, to heavy nuclei like gold, lead and uranium. Asymmetric collision combinations (e.g. protons against heavy ions) are also essential. For the creation, acceleration, and storage of bright intense ion beams, limits are set by space charge, charge change, and intrabeam scattering effects, as well as beam losses due to a variety of other phenomena. Currently, there are two operating ion colliders, the Relativistic Heavy Ion Collider (RHIC) at BNL, and the Large Hadron Collider (LHC) at CERN.

  1. Determination of Hazardous Chemicals by Microchip-based Field Asymmetric Waveform Ion Mobility Spectrometric Technology%芯片级高场非对称波形离子迁移谱技术检测危险品

    Institute of Scientific and Technical Information of China (English)

    张洁; 李灵锋; 郭大鹏; 张媛; 王琦; 李鹏; 汪小知

    2013-01-01

    An in-situ analytical procedure employing silicon chip based ultra high field asymmetric waveform ion mobility spectrometry(FAIMS) via direct sniffing was developed.The sample introduction temperature was 50 ℃.The carrier gas flow rate and the sample flow rate were 1500 mL/min and 100 mL/min respectively.Ten listed hazardous chemicals,which were prohibited for public transportation in China,were selected to verify the procedure in terms of validity,sensitivity and selectivity.Recognition algorithm was also developed for the FAIMS fingerprint spectral.Ten chemicals were resolved with high reproducibility at the concentration from 0.1 to 20 mg/L.In comparison with current competing instruments,the microchip-based FAIMS instrument,which features its simplicity,high sensitivity and selectivity,fast response and free of sample pretreatment,opens up new applications in the field of public security and homeland security.%建立了吸气法-芯片级高场非对称波形离子迁移谱(FAIMS)技术,设置进样温度为50℃,载气与样品气流量分别为1500和100 mL/min时,测定了10种国家交通部门规定严禁携带的易燃易爆危险品.实验结果表明,利用FAIMS技术可以有效检测多种危险品.实验得到了10种危险品的FAIMS图谱,并对其进行了指纹识别.利用扩散管辅助技术得到10种物质的检测浓度范围约为0.1 ~20 mg/L.此方法方便快速,灵敏度高,具有很好的应用前景.

  2. Development of salt waste treatment technology

    International Nuclear Information System (INIS)

    To develop a proper waste conditioning technology for salt wastes, alpha- contaminated organic wastes, and long-lived fission products, which are presumed to generate from the pyrochemical dry processing of spent fuel, researches on LiCl salt waste treatment (including salt fixation, ion exchange of radionuclides and salt pre-treatment technique), molten salt oxidation of organic alpha wastes and recovery of radioiodine have been performed. In a research on the waste LiCl salt treatment, the characterization on a salt-loaded zeolite sample, prepared by an immobilization of the molten LiCl salt waste with zeolite A, suggested that an optimum mixing ratio, r (=LiCl/zeolite) was 1.0. Pre-treatment of salt waste was performed via gelation reaction with additives of phosphate and sodium silicate. Characteristics of the gel product after drying and thermal treatment were tested and evaluated to establish the proper reaction conditions on the conversion of salt waste into durable waste forms. Molten salt oxidation (MSO) is selected as the most promising technology for the treatment of alpha-contaminated waste, and its lab-scale test and theoretical model study revealed its good effectiveness in the treatment of the problematic waste, such as halogenated organics including toxic and radioactive metals. The optimal conditions to effectively recover iodine from silver ion- exchanged adsorbent(AgX) was established and confirmed through experiment using radioiodine tracer. Fundamental data for conversion the recovered iodine to target material powder of NaI were obtained

  3. Fire behavior of carbonates-based electrolytes used in Li-ion rechargeable batteries with a focus on the role of the LiPF6 and LiFSI salts

    Science.gov (United States)

    Eshetu, Gebrekidan Gebresilassie; Bertrand, Jean-Pierre; Lecocq, Amandine; Grugeon, Sylvie; Laruelle, Stephane; Armand, Michel; Marlair, Guy

    2014-12-01

    A detailed investigation of the combustion behavior of LiPF6 or LiFSI-based carbonate electrolytes was conducted with the objective of getting better knowledge of lithium-ion battery system fire induced thermal and chemical threats. The well-controlled experimental conditions provided by the Tewarson calorimeter have enabled the accurate evaluation of fire hazard rating parameters such as heat release rate and effective heat of combustion and the quantification of toxic effluents (HF, SO2, NOx…). Results have shown that all the electrolytes tested burn in phases depending on the flammability nature of their mixture constituents. The first stage of combustion is solely governed by the more volatile solvent (linear carbonate) and the influence of adding salt comes into effect predominantly in the second stage. It has been also shown that combustion enthalpy of electrolytes lies in the solvent mixture, irrespective of the salt added. The fire induced toxicity in well-ventilated conditions is found to be mainly dictated by the salt and its chemical structure, showing very limited concerns that emanate from the organic solvents.

  4. Asymmetric information and economics

    Science.gov (United States)

    Frieden, B. Roy; Hawkins, Raymond J.

    2010-01-01

    We present an expression of the economic concept of asymmetric information with which it is possible to derive the dynamical laws of an economy. To illustrate the utility of this approach we show how the assumption of optimal information flow leads to a general class of investment strategies including the well-known Q theory of Tobin. Novel consequences of this formalism include a natural definition of market efficiency and an uncertainty principle relating capital stock and investment flow.

  5. Asymmetric Organocatalytic Cycloadditions

    DEFF Research Database (Denmark)

    Mose, Rasmus

    2016-01-01

    were pioneered by Otto Paul Hermann Diels and Kurt Alder who discovered what later became known as the Diels Alder reaction. The Diels Alder reaction is a [4+2] cycloaddition in which a π4 component reacts with a π2 component via a cyclic transition state to generate a 6 membered ring. This reaction...... reactions constitute the first organocatalytic asymmetric higher order cycloadditions and a rational for the periselectivity and stereoselectivity is provided based on experimental and computational investigations....

  6. Asymmetric extractions in orthodontics

    Directory of Open Access Journals (Sweden)

    Camilo Aquino Melgaço

    2012-04-01

    Full Text Available INTRODUCTION: Extraction decisions are extremely important in during treatment planning. In addition to the extraction decision orthodontists have to choose what tooth should be extracted for the best solution of the problem and the esthetic/functional benefit of the patient. OBJECTIVE: This article aims at reviewing the literature relating the advantages, disadvantages and clinical implications of asymmetric extractions to orthodontics. METHODS: Keywords were selected in English and Portuguese and the EndNote 9 program was used for data base search in PubMed, Web of Science (WSc and LILACS. The selected articles were case reports, original articles and prospective or retrospective case-control studies concerning asymmetrical extractions of permanent teeth for the treatment of malocclusions. CONCLUSION: According to the literature reviewed asymmetric extractions can make some specific treatment mechanics easier. Cases finished with first permanent molars in Class II or III relationship in one or both sides seem not to cause esthetic or functional problems. However, diagnosis knowledge and mechanics control are essential for treatment success.

  7. Asymmetric Evolutionary Games.

    Science.gov (United States)

    McAvoy, Alex; Hauert, Christoph

    2015-08-01

    Evolutionary game theory is a powerful framework for studying evolution in populations of interacting individuals. A common assumption in evolutionary game theory is that interactions are symmetric, which means that the players are distinguished by only their strategies. In nature, however, the microscopic interactions between players are nearly always asymmetric due to environmental effects, differing baseline characteristics, and other possible sources of heterogeneity. To model these phenomena, we introduce into evolutionary game theory two broad classes of asymmetric interactions: ecological and genotypic. Ecological asymmetry results from variation in the environments of the players, while genotypic asymmetry is a consequence of the players having differing baseline genotypes. We develop a theory of these forms of asymmetry for games in structured populations and use the classical social dilemmas, the Prisoner's Dilemma and the Snowdrift Game, for illustrations. Interestingly, asymmetric games reveal essential differences between models of genetic evolution based on reproduction and models of cultural evolution based on imitation that are not apparent in symmetric games. PMID:26308326

  8. Origin of Asymmetric Charge Partitioning in the Dissociation of Gas-Phase Protein Homodimers

    OpenAIRE

    Jurchen, John C.; Williams, Evan R.

    2003-01-01

    The origin of asymmetric charge and mass partitioning observed for gas-phase dissociation of multiply charged macromolecular complexes has been hotly debated. These experiments hold the potential to provide detailed information about the interactions between the macromolecules within the complex. Here, this unusual phenomenon of asymmetric charge partitioning is investigated for several protein homodimers. Asymmetric charge partitioning in these ions depends on a number of factors, including ...

  9. Probing the effect of different cross-sections in asymmetric collisions

    OpenAIRE

    Kaur, Deepinder; Kaur, Varinderjit; Kumar, Suneel

    2011-01-01

    We present a complete systematic theoretical study of multifragmentation for asymmetric colliding nuclei for heavy-ion reactions in the energy range between 50 MeV/nucleon and 1000 MeV/nucleon by using isospin dependent quantum molecular dynamics (IQMD) model. We have observed an interesting outcome for asymmetric colliding nuclei. The comparison between the symmetric and asymmetric colliding nuclei for the isospin independent cross section and isospin dependent cross section has been studied...

  10. Molten salt of lithium bis(fluorosulfonyl)imide (LiFSI)-potassium bis(fluorosulfonyl)imide (KFSI) as electrolyte for the natural graphite/LiFePO4 lithium-ion cell

    International Nuclear Information System (INIS)

    The binary eutectic mixture of lithium bis(fluorosulfonyl)imide (LiFSI) and potassium bis(fluorosulfonyl)imide (KFSI) with a molar ratio of xLiFSI: xKFSI = 0.41: 0.59 has been investigated as molten salt electrolyte for natural graphite/LiFePO4 lithium-ion cells at 80 °C. The electrochemical performances of the Li/natural graphite, Li/LiFePO4, and natural graphite/LiFePO4 cells using this molten salt electrolyte have been evaluated, in terms of cycling performances and electrochemical impedance spectra (EIS) at 80 °C. Both the Li/natural graphite and Li/LiFePO4 cells show good cycling performances. The initial specific capacities after conditioning for the natural graphite and LiFePO4 electrodes are 353 and 150 mAh g−1, respectively, and the corresponding capacity retention rates are 98% and 97%, respectively, after 100 cycles at 80 °C, except for a large irreversible capacity (162 mAh g−1) observed for the natural graphite at the first cycle for forming solid electrolyte interface (SEI) film. The natural graphite/LiFePO4 lithium-ion cell using this molten salt electrolyte shows a low capacity in the range of 71–86 mAh g−1, due to the large irreversible capacity (71 mAh g−1) at the first cycle, but it shows a good cycleability after the first cycle, and provides a specific capacity of 71 mAh g−1 after 100 cycles at 80 °C. The variations of cycling performances of these cells can be well correlated with their impedance evolution with cycling

  11. Synthesis and Properties of the Heterospin (S1 = S2 = (1)/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl.

    Science.gov (United States)

    Pushkarevsky, Nikolay A; Semenov, Nikolay A; Dmitriev, Alexey A; Kuratieva, Natalia V; Bogomyakov, Artem S; Irtegova, Irina G; Vasilieva, Nadezhda V; Bode, Bela E; Gritsan, Nina P; Konstantinova, Lidia S; Woollins, J Derek; Rakitin, Oleg A; Konchenko, Sergey N; Ovcharenko, Victor I; Zibarev, Andrey V

    2015-07-20

    Low-temperature interaction of [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazole (1) with MoMes2 (Mes = mesitylene/1,3,5-trimethylbenzene) in tetrahydrofuran gave the heterospin (S1 = S2 = (1)/2) radical-ion salt [MoMes2](+)[1](-) (2) whose structure was confirmed by single-crystal X-ray diffraction (XRD). The structure revealed alternating layers of the cations and anions with the Mes ligands perpendicular, and the anions tilted by 45°, to the layer plane. At 300 K the effective magnetic moment of 2 is equal to 2.40 μB (theoretically expected 2.45 μB) and monotonically decreases with lowering of the temperature. In the temperature range 2-300 K, the molar magnetic susceptibility of 2 is well-described by the Curie-Weiss law with parameters C and θ equal to 0.78 cm(3) K mol(-1) and -31.2 K, respectively. Overall, the magnetic behavior of 2 is similar to that of [CrTol2](+)[1](-) and [CrCp*2](+)[1](-), i.e., changing the cation [MAr2](+) 3d atom M = Cr (Z = 24) with weak spin-orbit coupling (SOC) to a 4d atom M = Mo (Z = 42) with stronger SOC does not affect macroscopic magnetic properties of the salts. For the XRD structure of salt 2, parameters of the Heisenberg spin-Hamiltonian were calculated using the broken-symmetry DFT and CASSCF approaches, and the complex 3D magnetic structure with both the ferromagnetic (FM) and antiferromagnetic (AF) exchange interactions was revealed with the latter as dominating. Salt 2 is thermally unstable and slowly loses the Mes ligands upon storage at ambient temperature. Under the same reaction conditions, interaction of 1 with MoTol2 (Tol = toluene) proceeded with partial loss of the Tol ligands to afford diamagnetic product. PMID:26121418

  12. The effect of organic salts on HPMC

    OpenAIRE

    Mongkolpiyawat, Jiraporn

    2012-01-01

    The presence of organic salts as drug counter-ions and buffers in hydroxypropylmethylcellulose (HPMC) matrices is often overlooked. This study investigates their potential to influence polymer solution properties and matrix drug release kinetics. A homologous series of aliphatic organic salts influenced solution and matrix properties in rank order of hydrocarbon chain length. Monovalent salts containing 1to4 C-atoms had little effect on polymer surface activity, but lowered sol:gel transit...

  13. Gene Expression, Protein Function and Pathways of Arabidopsis thaliana Responding to Silver Nanoparticles in Comparison to Silver Ions, Cold, Salt, Drought, and Heat

    Directory of Open Access Journals (Sweden)

    Eisa Kohan-Baghkheirati

    2015-03-01

    Full Text Available Silver nanoparticles (AgNPs have been widely used in industry due to their unique physical and chemical properties. However, AgNPs have caused environmental concerns. To understand the risks of AgNPs, Arabidopsis microarray data for AgNP, Ag+, cold, salt, heat and drought stresses were analyzed. Up- and down-regulated genes of more than two-fold expression change were compared, while the encoded proteins of shared and unique genes between stresses were subjected to differential enrichment analyses. AgNPs affected the fewest genes (575 in the Arabidopsis genome, followed by Ag+ (1010, heat (1374, drought (1435, salt (4133 and cold (6536. More genes were up-regulated than down-regulated in AgNPs and Ag+ (438 and 780, respectively while cold down-regulated the most genes (4022. Responses to AgNPs were more similar to those of Ag+ (464 shared genes, cold (202, and salt (163 than to drought (50 or heat (30; the genes in the first four stresses were enriched with 32 PFAM domains and 44 InterPro protein classes. Moreover, 111 genes were unique in AgNPs and they were enriched in three biological functions: response to fungal infection, anion transport, and cell wall/plasma membrane related. Despite shared similarity to Ag+, cold and salt stresses, AgNPs are a new stressor to Arabidopsis.

  14. Phosphate salts

    Science.gov (United States)

    ... for children 9-18 years of age. Phosphate salts are POSSIBLY UNSAFE if the amount of phosphate consumed (expressed as phosphorous) exceeds the tolerable upper intake level (UL). The ULs are 3 grams per day for children 1-8 years; and 4 grams per day ...

  15. Swelling of phospholipids by monovalent salt

    OpenAIRE

    Petrache, Horia I.; Tristram-Nagle, Stephanie; Harries, Daniel; Kučerka, Norbert; Nagle, John F.; Parsegian, V. Adrian

    2005-01-01

    Critical to biological processes such as membrane fusion and secretion, ion-lipid interactions at the membrane-water interface still raise many unanswered questions. Using reconstituted phosphatidylcholine membranes, we confirm here that multilamellar vesicles swell in salt solutions, a direct indication that salt modifies the interactions between neighboring membranes. By varying sample histories, and by comparing with data from ion carrier-containing bilayers, we eliminate the possibility t...

  16. H- beam emittance measurements for the penning and the asymmetric, grooved magnetron surface-plasma sources

    International Nuclear Information System (INIS)

    Beam-intensity and emittance measurements show that the H- beam from our Penning surface-plasma source (SPS) has twice the intensity and ten times the brightness of the H- beam from an asymmetric, grooved magnetron SPS. We deduce H- ion temperatures of 5 eV for the Penning SPS and 22 eV for the asymmetric, grooved magnetron

  17. Facilitated Asymmetric Exclusion

    OpenAIRE

    Gabel, Alan; Krapivsky, P. L.; Redner, S.

    2010-01-01

    We introduce a class of facilitated asymmetric exclusion processes in which particles are pushed by neighbors from behind. For the simplest version in which a particle can hop to its vacant right neighbor only if its left neighbor is occupied, we determine the steady state current and the distribution of cluster sizes on a ring. We show that an initial density downstep develops into a rarefaction wave that can have a jump discontinuity at the leading edge, while an upstep results in a shock w...

  18. Asymmetric synthesis v.4

    CERN Document Server

    Morrison, James

    1984-01-01

    Asymmetric Synthesis, Volume 4: The Chiral Carbon Pool and Chiral Sulfur, Nitrogen, Phosphorus, and Silicon Centers describes the practical methods of obtaining chiral fragments. Divided into five chapters, this book specifically examines initial chiral transmission and extension. The opening chapter describes the so-called chiral carbon pool, the readily available chiral carbon fragments used as building blocks in synthesis. This chapter also provides a list of 375 chiral building blocks, along with their commercial sources, approximate prices, and methods of synthesis. Schemes involving

  19. Application of Boron-Based Lithium Salt for Li-Ion Battery%硼基锂盐电解质在锂离子电池中的应用

    Institute of Scientific and Technical Information of China (English)

    仇卫华; 阎坤; 连芳; 乔亚非

    2011-01-01

    Electrolyte is considered as one of the key materials to decide the performance of Li-ion batteries.Novel boron-based lithium salts have attracted people' s interests because of its varieties and environmental-friendly property. Lithium bis(oxalato) borate (LiBOB) , as one of boron-based lithium salts, is believed to be a candidate for commercial LiPF6 due to its good film-forming property and high thermal stability. In the paper, the new development of boron-based lithium salts is introduced, and LiBOB is also evaluated as lithium salt of electrolyte for Li-ion battery. The main influencing factors of LiBOB-based electrolyte are summarized. Especially, it has focused on the compatibility of LiBOB-based electrolyte with anode and metal oxide cathode. The application of LiBOBbased polymer electrolyte and LiBOB plastic chip electrolyte are introduced.%电解质材料是锂离子电池的关键材料之一,它直接影响电池的性能.新型硼酸锂盐由于种类繁多且环境友好而越来越引起人们的重视.双草酸硼酸锂(LiBOB)是一种新型的锂盐,具有很好的成膜性能和热稳定性,是一种很有潜力替代现有商品化锂盐LiPF6的物质.本文介绍了近期新型硼基锂盐的发展状况,归纳了LiBOB基电解质的研究概况,综述了影响LiBOB基电解质的因素,讨论了LiBOB与正负极材料的相容性,并对LiBOB基聚合物电解质和LiBOB塑晶电解质的应用进行了介绍.

  20. Effect of iron salt counter ion in dose-response curves for inactivation of Fusarium solani in water through solar driven Fenton-like processes

    Science.gov (United States)

    Aurioles-López, Verónica; Polo-López, M. Inmaculada; Fernández-Ibáñez, Pilar; López-Malo, Aurelio; Bandala, Erick R.

    2016-02-01

    The inactivation of Fusarium solani in water was assessed by solar driven Fenton-like processes using three different iron salts: ferric acetylacetonate (Fe(acac)3), ferric chloride (FeCl3) and ferrous sulfate (FeSO4). The experimental conditions tested were [Fe] ≈ 5 mg L-1, [H2O2] ≈ 10 mg L-1 and [Fe] ≈ 10 mg L-1; [H2O2] ≈ 20 mg L-1 mild and high, respectively, and pH 3.0 and 5.0, under solar radiation. The highest inactivation rates were observed at high reaction conditions for the three iron salts tested at pH 5.0 with less than 3.0 kJ L-1 of accumulate energy (QUV) to achieve over 99.9% of F. solani inactivation. Fe(acac)3 was the best iron salt to accomplishing F. solani inactivation. The modified Fermi equation was used to fix the experimental inactivation, data showed it was helpful for modeling the process, adequately describing dose-response curves. Inactivation process using FeSO4 at pH 3.0 was modeled fairly with r2 = 0.98 and 0.99 (mild and high concentration, respectively). Fe(acac)3, FeCl3 and FeSO4 at high concentration (i.e. [Fe] ≈ 10 mg L-1; [H2O2] ≈ 20 mg L-1) and pH 5.0 showed the highest fitting values (r2 = 0.99). Iron salt type showed a remarkable influence on the Fenton-like inactivation process.

  1. RHIC operation with asymmetric collisions in 2015

    Energy Technology Data Exchange (ETDEWEB)

    Liu, C. [Brookhaven National Lab. (BNL), Upton, NY (United States); Aschenauer, C. [Brookhaven National Lab. (BNL), Upton, NY (United States); Atoian, G. [Brookhaven National Lab. (BNL), Upton, NY (United States); Blaskiewicz, M. [Brookhaven National Lab. (BNL), Upton, NY (United States); Brown, K. A. [Brookhaven National Lab. (BNL), Upton, NY (United States); Bruno, D. [Brookhaven National Lab. (BNL), Upton, NY (United States); Connolly, R. [Brookhaven National Lab. (BNL), Upton, NY (United States); Ottavio, T. D. [Brookhaven National Lab. (BNL), Upton, NY (United States); Drees, K. A. [Brookhaven National Lab. (BNL), Upton, NY (United States); Fischer, W. [Brookhaven National Lab. (BNL), Upton, NY (United States); Gardner, C. J. [Brookhaven National Lab. (BNL), Upton, NY (United States); Gu, X. [Brookhaven National Lab. (BNL), Upton, NY (United States); Hayes, T. [Brookhaven National Lab. (BNL), Upton, NY (United States); Huang, H. [Brookhaven National Lab. (BNL), Upton, NY (United States); Laster, J. S. [Brookhaven National Lab. (BNL), Upton, NY (United States); Luo, Y. [Brookhaven National Lab. (BNL), Upton, NY (United States); Makdisi, Y. [Brookhaven National Lab. (BNL), Upton, NY (United States); Marr, G. [Brookhaven National Lab. (BNL), Upton, NY (United States); Marusic, A. [Brookhaven National Lab. (BNL), Upton, NY (United States); Meot, F. [Brookhaven National Lab. (BNL), Upton, NY (United States); Mernick, K. [Brookhaven National Lab. (BNL), Upton, NY (United States); Michnoff, R. [Brookhaven National Lab. (BNL), Upton, NY (United States); Minty, M. [Brookhaven National Lab. (BNL), Upton, NY (United States); Montag, C. [Brookhaven National Lab. (BNL), Upton, NY (United States); Morris, J. [Brookhaven National Lab. (BNL), Upton, NY (United States); Narayan, G. [Brookhaven National Lab. (BNL), Upton, NY (United States); Nayak, S. [Brookhaven National Lab. (BNL), Upton, NY (United States); Nemesure, S. [Brookhaven National Lab. (BNL), Upton, NY (United States); Pile, P. [Brookhaven National Lab. (BNL), Upton, NY (United States); Poblaguev, A. [Brookhaven National Lab. (BNL), Upton, NY (United States); Ranjbar, V. [Brookhaven National Lab. (BNL), Upton, NY (United States); Robert-Demolaize, G. [Brookhaven National Lab. (BNL), Upton, NY (United States); Roser, T. [Brookhaven National Lab. (BNL), Upton, NY (United States); Schmidke, B. [Brookhaven National Lab. (BNL), Upton, NY (United States); Schoefer, V. [Brookhaven National Lab. (BNL), Upton, NY (United States); Severino, F. [Brookhaven National Lab. (BNL), Upton, NY (United States); Shrey, T. [Brookhaven National Lab. (BNL), Upton, NY (United States); Smith, K. [Brookhaven National Lab. (BNL), Upton, NY (United States); Steski, D. [Brookhaven National Lab. (BNL), Upton, NY (United States); Tepikian, S. [Brookhaven National Lab. (BNL), Upton, NY (United States); Trbojevic, D. [Brookhaven National Lab. (BNL), Upton, NY (United States); Tsoupas, N. [Brookhaven National Lab. (BNL), Upton, NY (United States); Wang, G. [Brookhaven National Lab. (BNL), Upton, NY (United States); White, S. [Brookhaven National Lab. (BNL), Upton, NY (United States); Yip, K. [Brookhaven National Lab. (BNL), Upton, NY (United States); Zaltsman, A. [Brookhaven National Lab. (BNL), Upton, NY (United States); Zeno, K. [Brookhaven National Lab. (BNL), Upton, NY (United States); Zhang, S. Y. [Brookhaven National Lab. (BNL), Upton, NY (United States)

    2015-08-07

    To study low-x shadowing/saturation physics as well as other nuclear effects [1], [2], proton-gold (p-Au, for 5 weeks) and proton-Aluminum (p-Al, for 2 weeks) collisions were provided for experiments in 2015 at the Relativistic Heavy Ion Collider (RHIC), with polarized proton beam in the Blue ring and Au/Al beam in the Yellow ring. The special features of the asymmetric run in 2015 will be introduced. The operation experience will be reviewed as well in the report.

  2. Crystal structure of the heptamolybdate(VI) (paramolybdate) ion, [Mo7O24]6-, in the ammonium and potassium tetrahydrate salts

    Science.gov (United States)

    Evans, H.T., Jr.; Gatehouse, B.M.; Leverett, P.

    1975-01-01

    The crystal structures of the isomorphous salts MI6 [Mo7O24],4H2O (M = NH4 or K) have been refined by three-dimensional X-ray diffraction methods. Unit cell dimensions of these monoclinic compounds, space group P21/C with Z = 4, are, ammonium salt: a = 8.3934 ?? 0.0008, b = 36.1703 ?? 0.0045, c = 10.4715 ?? 0.0011 A??, ?? = 115.958?? ?? 0.008??; and potassium salt: a = 8.15 ?? 0.02, b = 35.68 ?? 0.1, c = 10.30 ?? 0.02 A??, ?? = 115.2?? ?? 02??. By use of multiple Weissenberg patterns, 8197 intensity data (Mo-K?? radiation) for the ammonium compound and 2178 (Cu-K?? radiation) for the potassium compound were estimated visually and used to test and refine Lindqvist's proposed structure in the space group P21/c. Lindqvist's structure was confirmed and the full matrix least-squares isotropic refinement led to R 0.076 (ammonium) 0.120 (potassium), with direct unambiguous location of the cations and water molecules in the potassium compound.

  3. Asymmetric quantum cloning machines

    International Nuclear Information System (INIS)

    A family of asymmetric cloning machines for quantum bits and N-dimensional quantum states is introduced. These machines produce two approximate copies of a single quantum state that emerge from two distinct channels. In particular, an asymmetric Pauli cloning machine is defined that makes two imperfect copies of a quantum bit, while the overall input-to-output operation for each copy is a Pauli channel. A no-cloning inequality is derived, characterizing the impossibility of copying imposed by quantum mechanics. If p and p' are the probabilities of the depolarizing channels associated with the two outputs, the domain in (√p,√p')-space located inside a particular ellipse representing close-to-perfect cloning is forbidden. This ellipse tends to a circle when copying an N-dimensional state with N→∞, which has a simple semi-classical interpretation. The symmetric Pauli cloning machines are then used to provide an upper bound on the quantum capacity of the Pauli channel of probabilities px, py and pz. The capacity is proven to be vanishing if (√px, √py, √pz) lies outside an ellipsoid whose pole coincides with the depolarizing channel that underlies the universal cloning machine. Finally, the tradeoff between the quality of the two copies is shown to result from a complementarity akin to Heisenberg uncertainty principle. (author)

  4. Asymmetric inclusion process

    Science.gov (United States)

    Reuveni, Shlomi; Eliazar, Iddo; Yechiali, Uri

    2011-10-01

    We introduce and explore the asymmetric inclusion process (ASIP), an exactly solvable bosonic counterpart of the fermionic asymmetric exclusion process (ASEP). In both processes, random events cause particles to propagate unidirectionally along a one-dimensional lattice of n sites. In the ASEP, particles are subject to exclusion interactions, whereas in the ASIP, particles are subject to inclusion interactions that coalesce them into inseparable clusters. We study the dynamics of the ASIP, derive evolution equations for the mean and probability generating function (PGF) of the sites’ occupancy vector, obtain explicit results for the above mean at steady state, and describe an iterative scheme for the computation of the PGF at steady state. We further obtain explicit results for the load distribution in steady state, with the load being the total number of particles present in all lattice sites. Finally, we address the problem of load optimization, and solve it under various criteria. The ASIP model establishes bridges between statistical physics and queueing theory as it represents a tandem array of queueing systems with (unlimited) batch service, and a tandem array of growth-collapse processes.

  5. Molten salt synthesis of potassium hexatitanate

    Science.gov (United States)

    Zaremba, T.

    2012-09-01

    Potassium hexatitanate fibrous crystals have been synthesized by a conventional solid-state reaction and via molten salt process. The molten salt process has been shown to be effective in preparing fine and non-agglomerated K2Ti6O13 whiskers. The type of molten salt (KCl, NaCl-KCl) has a significant effect on the chemical composition of the whiskers. By using a eutectic mixture of NaCl and KCl, the replacement of potassium ions in solid potassium hexatitanate by smaller sodium ions from the chloride flux can be achieved. The characterization of the samples was carried out by means of XRD, SEM, EDX and WDX.

  6. Liquid-liquid extraction of ion-association complexes of cobalt(II)-4-(2-pyridylazo)resorcinol with ditetrazolium salts

    OpenAIRE

    Divarova Vidka V.; Stojnova Kirila T.; Racheva Petya V.; Lekova Vanya D.; Dimitrov Atanas N.

    2015-01-01

    The formation and liquid-liquid extraction of ion-association complexes between Co(II)-4-(2-Pyridylazo)resorcinol (PAR) anionic chelates and cations of three ditetrazolium chlorides were studied: Blue Tetrazolium chloride (BTC), Neotetrazolium chloride (NTC) and Nitro Blue Tetrazolium chloride (NBT). The optimum conditions for the formation and solvent extraction of the ion-association comlpex chelates were determined. It has been found that in the systems ...

  7. Alternative Asymmetric Stochastic Volatility Models

    NARCIS (Netherlands)

    M. Asai (Manabu); M.J. McAleer (Michael)

    2010-01-01

    textabstractThe stochastic volatility model usually incorporates asymmetric effects by introducing the negative correlation between the innovations in returns and volatility. In this paper, we propose a new asymmetric stochastic volatility model, based on the leverage and size effects. The model is

  8. 锂离子电池电解质锂盐的发展历程和新型锂盐的研究进展%Development of Lithium Ion Battery Electrolyte and Research Progress of Novel Lithium Salts

    Institute of Scientific and Technical Information of China (English)

    闫春生; 李媛媛; 刘园园

    2016-01-01

    LiPF6 has become the most widely used commercial lithium battery electrolyte with brilliant ion-ic conductivity,better oxidation stability and less environmental pollution etc. Because LiPF6 thermal sta-bility is poor,the price is relatively expensive,the development and preparation of new lithium salts be-come a focus of attention for researchers. In this paper,the development of traditional lithium electrolyte is reviewed,the synthesis process of LiPF6 is summarized ,and research progress of new lithium salts is in-troduced.%六氟磷酸锂( LiPF6)因其突出的离子电导率、较优的氧化稳定性和较小的环境污染等优点成为目前使用最广泛的商业化锂电池电解质。由于LiPF6热稳定性较差、价格相对昂贵,使得新型锂盐的开发与制备成为研究者们关注的热点。本文回顾了传统锂盐电解质的发展,对LiPF6的合成工艺进行了综述,并介绍了新型锂盐的研究进展情况。

  9. 锂盐浓度对高功率锂离子电池性能的影响%Effect of lithium salt concentration on performance of high-rate discharge Li-ion battery

    Institute of Scientific and Technical Information of China (English)

    袁卉军; 陈真; 刘建生; 王姣丽

    2012-01-01

    考察了电解液中锂盐浓度对高功率锂离子电池倍率放电及高低温性能的影响.锂盐浓度为0.9~1.5 mol/L时,浓度越高越有利于大电流放电,但高于1.4 mol/L后,倍率放电中值电压的提升趋向平缓;在-20℃下以170 mA(1 C)放电,1.2 mol/L时的性能最好.%Effects of lithium salt concentration on rate discharge, high-low temperature performance of high-rate discharge Li-ion battery were investigated. When the lithium salt concentration was 0.9 ~ 1.5 mol/L, the higher concentration was benefit to heavy load discharge, but when higher than 1.4 mol/L, the increasing of rate discharge middle voltage trended gentle. When discharged with 1 C (170 mA) at - 20℃, the performance was the best with 1.2 mol/L.

  10. Engineered Asymmetric Synthetic Vesicles

    Science.gov (United States)

    Lu, Li; Chiarot, Paul

    2013-11-01

    Synthetic vesicles are small, fluid-filled spheres that are enclosed by a bilayer of lipid molecules. They can be used as models for investigating membrane biology and as delivery vehicles for pharmaceuticals. In practice, it is difficult to simultaneously control membrane asymmetry, unilamellarity, vesicle size, vesicle-to-vesicle uniformity, and luminal content. Membrane asymmetry, where each leaflet of the bilayer is composed of different lipids, is of particular importance as it is a feature of most natural membranes. In this study, we leverage microfluidic technology to build asymmetric vesicles at high-throughput. We use the precise flow control offered by microfluidic devices to make highly uniform emulsions, with controlled internal content, that serve as templates to build the synthetic vesicles. Flow focusing, dielectrophoretic steering, and interfacial lipid self-assembly are critical procedures performed on-chip to produce the vesicles. Fluorescent and confocal microscopy are used to evaluate the vesicle characteristics.

  11. Asymmetric black dyonic holes

    Directory of Open Access Journals (Sweden)

    I. Cabrera-Munguia

    2015-04-01

    Full Text Available A 6-parametric asymptotically flat exact solution, describing a two-body system of asymmetric black dyons, is studied. The system consists of two unequal counterrotating Kerr–Newman black holes, endowed with electric and magnetic charges which are equal but opposite in sign, separated by a massless strut. The Smarr formula is generalized in order to take into account their contribution to the mass. The expressions for the horizon half-length parameters σ1 and σ2, as functions of the Komar parameters and of the coordinate distance, are displayed, and the thermodynamic properties of the two-body system are studied. Furthermore, the seven physical parameters satisfy a simple algebraic relation which can be understood as a dynamical scenario, in which the physical properties of one body are affected by the ones of the other body.

  12. Asymmetric twin Dark Matter

    International Nuclear Information System (INIS)

    We study a natural implementation of Asymmetric Dark Matter in Twin Higgs models. The mirroring of the Standard Model strong sector suggests that a twin baryon with mass around 5 GeV is a natural Dark Matter candidate once a twin baryon number asymmetry comparable to the SM asymmetry is generated. We explore twin baryon Dark Matter in two different scenarios, one with minimal content in the twin sector and one with a complete copy of the SM, including a light twin photon. The essential requirements for successful thermal history are presented, and in doing so we address some of the cosmological issues common to many Twin Higgs models. The required interactions we introduce predict signatures at direct detection experiments and at the LHC

  13. Organizing for Asymmetric Collaboration

    DEFF Research Database (Denmark)

    Nielsen, Jørn Flohr; Sørensen, Henrik B.

    meet each other. On the contrary, we assume that asymmetry is both important and normal; moreover, asymmetry should be considered to be more complex than economists indicate with their concept of asymmetric information. Thus, the aim of the paper is to explore how asymmetries related to partners......  The vision of new organizational forms consists of less-organized networks and alliances between organizations, in which collaborative capabilities are assumed to be crucial (Miles et al., 2005). The path to such new forms may go through fragile cooperative efforts. Despite the good will of many......' different motives and different situational factors appear in an interorganizational setting. We classify interfaces according to the symmetry/asymmetry in the respective parent organizations' resources, commitment, and control of representatives and indicate how  classification schemes can be used to...

  14. Annihilating Asymmetric Dark Matter

    CERN Document Server

    Bell, Nicole F; Shoemaker, Ian M

    2014-01-01

    The relic abundance of particle and antiparticle dark matter (DM) need not be vastly different in thermal asymmetric dark matter (ADM) models. By considering the effect of a primordial asymmetry on the thermal Boltzmann evolution of coupled DM and anti-DM, we derive the requisite annihilation cross section. This is used in conjunction with CMB and Fermi-LAT gamma-ray data to impose a limit on the number density of anti-DM particles surviving thermal freeze-out. When the extended gamma-ray emission from the Galactic Center is reanalyzed in a thermal ADM framework, we find that annihilation into $\\tau$ leptons prefer anti-DM number densities 1-4$\\%$ that of DM while the $b$-quark channel prefers 50-100$\\%$.

  15. Ranking of 11 coastal halophytes from salt marshes in northwest Turkey according their salt tolerance

    OpenAIRE

    Zörb, Christian; Sümer, Ali; Sungur, Ali; Flowers, Timothy J.; ÖZCAN, Hasan

    2013-01-01

    Salt-affected soils with high electrolyte contents limit the development of the majority of plants and serve as a habitat only for such species (halophytes) that can survive the conditions. To date, there is still much that is unknown about the physiological mechanisms, including ion relationships, that make plants salt-resistant. The primary aim of this study was to evaluate a method of ranking plants for their salt tolerance. A total of 11 coastal halophytes of the Kavak Delta were evaluate...

  16. Hydrogen bonding in the crystal structure of the molecular salt of pyrazole–pyrazolium picrate

    Science.gov (United States)

    Su, Ping; Song, Xue-gang; Sun, Ren-qiang; Xu, Xing-man

    2016-01-01

    The asymmetric unit of the title organic salt [systematic name: 1H-pyrazol-2-ium 2,4,6-tri­nitro­phenolate–1H-pyrazole (1/1)], H(C3H4N2)2 +·C6H2N3O7 −, consists of one picrate anion and one hydrogen-bonded dimer of a pyrazolium monocation. The H atom involved in the dimer N—H⋯N hydrogen bond is disordered over both symmetry-unique pyrazole mol­ecules with occupancies of 0.52 (5) and 0.48 (5). In the crystal, the component ions are linked into chains along [100] by two different bifurcated N—H⋯(O,O) hydrogen bonds. In addition, weak C—H⋯O hydrogen bonds link inversion-related chains, forming columns along [100]. PMID:27308060

  17. Acumulación de iones y solutos orgánicos en dos genotipos de caña de azúcar, estresados con sales simples o suplementadas con calcio Ion and organic solute accumulation in two sugarcane genotypes, salt stressed with or without calcium supply

    Directory of Open Access Journals (Sweden)

    Marina García

    2009-04-01

    Full Text Available Se evaluaron dos genotipos de caña de azúcar que difieren en tolerancia salina (‘PR692176’, tolerante y ‘V78-1’, sensible, a fin de definir el papel de la exclusión de Na+ y/o de Cl-, de la selectividad K/Na, y de la acumulación de solutos orgánicos en su tolerancia salina diferencial. Las plantas crecieron en condiciones controladas durante cuatro meses y en los dos últimos meses se sometieron a estrés con sales simples de sodio, con o sin suplementación adicional de calcio. Se determinó la concentración de Na+, K+, Cl-, azúcares solubles y prolina en raíces y en hojas con edad distinta. En las plantas estresadas la concentración foliar de K+ se redujo y la de Na+ y/o Cl- se incrementó, pero los dos últimos iones se acumularon preferentemente en las hojas más maduras y en la vaina foliar. La concentración foliar de Na+ en las plantas estresadas con NaCl, fue mayor que en las estresadas con Na2SO4. La suplementación con calcio incrementó la concentración de K+ y redujo la de Na+ y/o de Cl-. El contenido de azúcares no reductores y de prolina se incrementó con la salinidad en ambos genotipos. Bajo estrés salino PR692176 mantuvo menor concentración foliar de Na+ y de Cl-, mayor relación K/Na en las hojas, y acumuló mayor contenido de azúcares no reductores que V78-1. Estos resultados indican que la tolerancia salina en caña de azúcar está relacionada con una mejor capacidad de exclusión, y una mayor habilidad para acumular azúcares no reductores para ajuste osmótico.Two sugar cane genotypes differing in salt tolerance (‘PR692176’, salt tolerant and ‘V78-1’, salt sensitive were evaluated to know the role of the Na+ and/or Cl- exclusion, the K/Na selectivity, and the accumulation of organic solutes in their differential salt tolerance. The plants grew four months under controlled conditions, and during the last two months, they were subjected to salt stress using simple sodium salts, with or without

  18. Surfactant protein C peptides with salt-bridges (“ion-locks” promote high surfactant activities by mimicking the α-helix and membrane topography of the native protein

    Directory of Open Access Journals (Sweden)

    Frans J. Walther

    2014-07-01

    Full Text Available Background. Surfactant protein C (SP-C; 35 residues in lungs has a cationic N-terminal domain with two cysteines covalently linked to palmitoyls and a C-terminal region enriched in Val, Leu and Ile. Native SP-C shows high surface activity, due to SP-C inserting in the bilayer with its cationic N-terminus binding to the polar headgroup and its hydrophobic C-terminus embedded as a tilted, transmembrane α-helix. The palmitoylcysteines in SP-C act as ‘helical adjuvants’ to maintain activity by overriding the β-sheet propensities of the native sequences. Objective. We studied SP-C peptides lacking palmitoyls, but containing glutamate and lysine at 4-residue intervals, to assess whether SP-C peptides with salt-bridges (“ion-locks” promote surface activity by mimicking the α-helix and membrane topography of native SP-C. Methods. SP-C mimics were synthesized that reproduce native sequences, but without palmitoyls (i.e., SP-Css or SP-Cff, with serines or phenylalanines replacing the two cysteines. Ion-lock SP-C molecules were prepared by incorporating single or double Glu−–Lys+ into the parent SP-C’s. The secondary structures of SP-C mimics were studied with Fourier transform infrared (FTIR spectroscopy and PASTA, an algorithm that predicts β-sheet propensities based on the energies of the various β-sheet pairings. The membrane topography of SP-C mimics was investigated with orientated and hydrogen/deuterium (H/D exchange FTIR, and also Membrane Protein Explorer (MPEx hydropathy analysis. In vitro surface activity was determined using adsorption surface pressure isotherms and captive bubble surfactometry, and in vivo surface activity from lung function measures in a rabbit model of surfactant deficiency. Results. PASTA calculations predicted that the SP-Css and SP-Cff peptides should each form parallel β-sheet aggregates, with FTIR spectroscopy confirming high parallel β-sheet with ‘amyloid-like’ properties. The enhanced

  19. 不同盐度胁迫对芦荟生长和离子吸收分配的影响%Effects of Salt Concentration on Growth, Ion Absorption and Distribution of Aloe vera L.

    Institute of Scientific and Technical Information of China (English)

    马艳萍

    2012-01-01

    为探索芦荟对微咸水灌溉栽培的适应性,研究不同盐浓度对其生长和离子吸收分配的影响.结果表明,长期(120天)以含盐溶液灌溉栽培,盐浓度达200 mmol/L NaCl显著抑制芦荟生长,100 mmol/LNaCl对芦荟生长的抑制作用显著减轻,50 mmol/L NaCl不抑制芦荟生长.同时,以50 mmol/L NaCl溶液灌溉对芦荟盐分离子吸收分配影响轻微,但盐浓度达100 mmol/LNaCl对芦荟影响显著:根、茎、叶中K+含量显著下降,Na+、Cl-含量显著增大,K+/Na+大幅减小.X-射线能谱分析结果进一步表明,叶片贮水组织是芦荟积累盐分离子的重要部位,但100 mmol/L NaCl胁迫下芦荟根尖和叶片细胞中的离子平衡受到显著干扰.结果说明,芦荟适于用微咸水灌溉栽培,叶片贮水组织在缓解其盐胁迫中可起重要作用.%To explore the adaptability of irrigating aloe with weakly brine water, the effects of different concentration salinity stresses on growth, ion absorption and distribution of aloe plants were investigated.Experimental results showed that irrigation with 200 mmol/L NaCl for 120 d significantly retarded aloe growth, but the negative effects of irrigating aloe with 100 mmol/L NaCl on aloe growth were significantly relieved, even irrigating with 50 mmol/L NaCl did not retard aloe growth.The effects of irrigating with 50 mmol/L NaCl on ion absorption, transportation and distribution of aloe plants were not significant, but irrigating with 100 mmol/L NaCl were significant: K + contents of root, stem and leaf significantly decreased, Na + and Cl- content significantly increased, K+Na+ ratio significantly decreased.X-ray microanalysis results further showed that leaf aqueous was a main part of accumulating salt ion but ion homeostasis in root and leaf cells of aloe plants were significantly interrupted under 100 mmol/L NaCl stress.The experiment results suggested that Aloe vera L.was suitable to be irrigated with weakly brine water, and leaf

  20. Metal rolling - Asymmetrical rolling process

    Science.gov (United States)

    Alexa, V.; Raţiu, S.; Kiss, I.

    2016-02-01

    The development of theory and practice related to the asymmetric longitudinal rolling process is based on the general theory of metalworking by pressure and symmetric rolling theory, to which a large number of scientists brought their contribution. The rolling of metal materials was a serious problem throughout history, either economically or technically, because the plating technologies enabled the consumption of raw materials (scarce and expensive) to be reduced, while improving the mechanical properties. Knowing the force parameters related to asymmetric rolling leads to the optimization of energy and raw material consumption. This paper presents data on symmetric rolling process, in order to comparatively highlight the particularities of the asymmetric process.

  1. Asymmetric Gepner Models (Revisited)

    CERN Document Server

    Gato-Rivera, B

    2010-01-01

    We reconsider a class of heterotic string theories studied in 1989, based on tensor products of N=2 minimal models with asymmetric simple current invariants. We extend this analysis from (2,2) and (1,2) spectra to (0,2) spectra with SO(10) broken to the Standard Model. In the latter case the spectrum must contain fractionally charged particles. We find that in nearly all cases at least some of them are massless. However, we identify a large subclass where the fractional charges are at worst half-integer, and often vector-like. The number of families is very often reduced in comparison to the 1989 results, but there are no new tensor combinations yielding three families. All tensor combinations turn out to fall into two classes: those where the number of families is always divisible by three, and those where it is never divisible by three. We find an empirical rule to determine the class, which appears to extend beyond minimal N=2 tensor products. We observe that distributions of physical quantities such as th...

  2. Magnetically Modified Asymmetric Supercapacitors Project

    Data.gov (United States)

    National Aeronautics and Space Administration — This Small Business Innovation Research Phase I project is for the development of an asymmetric supercapacitor that will have improved energy density and cycle...

  3. Active Matter on Asymmetric Substrates

    OpenAIRE

    Reichhardt, C. J. Olson; Drocco, J.; Mai, T.; Wan, M. B.; Reichhardt, C.

    2011-01-01

    For collections of particles in a thermal bath interacting with an asymmetric substrate, it is possible for a ratchet effect to occur where the particles undergo a net dc motion in response to an ac forcing. Ratchet effects have been demonstrated in a variety of systems including colloids as well as magnetic vortices in type-II superconductors. Here we examine the case of active matter or self-driven particles interacting with asymmetric substrates. Active matter systems include self-motile c...

  4. Mobile Termination with Asymmetric Networks

    OpenAIRE

    Dewenter, Ralf; Haucap, Justus

    2003-01-01

    This paper examines mobile termination fees and their regulation when networks are asymmetric in size. It is demonstrated that with consumer ignorance about the exact termination rates (a) a mobile network?s termination rate is the higher the smaller the network?s size (as measured through its subscriber base) and (b) asymmetric regulation of only the larger operators in a market will, ce-teris paribus, induce the smaller operators to increase their termination rates. The results are supporte...

  5. Multicatalyst system in asymmetric catalysis

    CERN Document Server

    Zhou, Jian

    2014-01-01

    This book introduces multi-catalyst systems by describing their mechanism and advantages in asymmetric catalysis.  Helps organic chemists perform more efficient catalysis with step-by-step methods  Overviews new concepts and progress for greener and economic catalytic reactions  Covers topics of interest in asymmetric catalysis including bifunctional catalysis, cooperative catalysis, multimetallic catalysis, and novel tandem reactions   Has applications for pharmaceuticals, agrochemicals, materials, and flavour and fragrance

  6. Asymmetric Dark Matter from Leptogenesis

    OpenAIRE

    Falkowski, Adam; Ruderman, Joshua T.; Volansky, Tomer

    2011-01-01

    We present a new realization of asymmetric dark matter in which the dark matter and lepton asymmetries are generated simultaneously through two-sector leptogenesis. The right-handed neutrinos couple both to the Standard Model and to a hidden sector where the dark matter resides. This framework explains the lepton asymmetry, dark matter abundance and neutrino masses all at once. In contrast to previous realizations of asymmetric dark matter, the model allows for a wide range of dark matter mas...

  7. Excluded volume and ion-ion correlation effects on the ionic atmosphere around B-DNA: Theory, simulations, and experiments

    Energy Technology Data Exchange (ETDEWEB)

    Ovanesyan, Zaven; Marucho, Marcelo, E-mail: marcelo.marucho@utsa.edu [Department of Physics and Astronomy, The University of Texas at San Antonio, San Antonio, Texas 78249-5003 (United States); Medasani, Bharat [Department of Physics and Astronomy, The University of Texas at San Antonio, San Antonio, Texas 78249-5003 (United States); Computational Research Division, Lawrence Berkeley National Lab, Berkeley, California 94700 (United States); Fenley, Marcia O. [Institute of Molecular Biophysics, Florida State University, Tallahassee, Florida 32306 (United States); Guerrero-García, Guillermo Iván [Instituto de Física, Universidad Autónoma de San Luis Potosí, Álvaro Obregón 64, 78000 San Luis Potosí, San Luis Potosí (Mexico); Department of Chemistry and Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208 (United States); Olvera de la Cruz, Mónica [Department of Chemistry and Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208 (United States)

    2014-12-14

    The ionic atmosphere around a nucleic acid regulates its stability in aqueous salt solutions. One major source of complexity in biological activities involving nucleic acids arises from the strong influence of the surrounding ions and water molecules on their structural and thermodynamic properties. Here, we implement a classical density functional theory for cylindrical polyelectrolytes embedded in aqueous electrolytes containing explicit (neutral hard sphere) water molecules at experimental solvent concentrations. Our approach allows us to include ion correlations as well as solvent and ion excluded volume effects for studying the structural and thermodynamic properties of highly charged cylindrical polyelectrolytes. Several models of size and charge asymmetric mixtures of aqueous electrolytes at physiological concentrations are studied. Our results are in good agreement with Monte Carlo simulations. Our numerical calculations display significant differences in the ion density profiles for the different aqueous electrolyte models studied. However, similar results regarding the excess number of ions adsorbed to the B-DNA molecule are predicted by our theoretical approach for different aqueous electrolyte models. These findings suggest that ion counting experimental data should not be used alone to validate the performance of aqueous DNA-electrolyte models.

  8. Excluded volume and ion-ion correlation effects on the ionic atmosphere around B-DNA: Theory, simulations, and experiments

    International Nuclear Information System (INIS)

    The ionic atmosphere around a nucleic acid regulates its stability in aqueous salt solutions. One major source of complexity in biological activities involving nucleic acids arises from the strong influence of the surrounding ions and water molecules on their structural and thermodynamic properties. Here, we implement a classical density functional theory for cylindrical polyelectrolytes embedded in aqueous electrolytes containing explicit (neutral hard sphere) water molecules at experimental solvent concentrations. Our approach allows us to include ion correlations as well as solvent and ion excluded volume effects for studying the structural and thermodynamic properties of highly charged cylindrical polyelectrolytes. Several models of size and charge asymmetric mixtures of aqueous electrolytes at physiological concentrations are studied. Our results are in good agreement with Monte Carlo simulations. Our numerical calculations display significant differences in the ion density profiles for the different aqueous electrolyte models studied. However, similar results regarding the excess number of ions adsorbed to the B-DNA molecule are predicted by our theoretical approach for different aqueous electrolyte models. These findings suggest that ion counting experimental data should not be used alone to validate the performance of aqueous DNA-electrolyte models

  9. Excluded volume and ion-ion correlation effects on the ionic atmosphere around B-DNA: theory, simulations, and experiments.

    Science.gov (United States)

    Ovanesyan, Zaven; Medasani, Bharat; Fenley, Marcia O; Guerrero-García, Guillermo Iván; de la Cruz, Mónica Olvera; Marucho, Marcelo

    2014-12-14

    The ionic atmosphere around a nucleic acid regulates its stability in aqueous salt solutions. One major source of complexity in biological activities involving nucleic acids arises from the strong influence of the surrounding ions and water molecules on their structural and thermodynamic properties. Here, we implement a classical density functional theory for cylindrical polyelectrolytes embedded in aqueous electrolytes containing explicit (neutral hard sphere) water molecules at experimental solvent concentrations. Our approach allows us to include ion correlations as well as solvent and ion excluded volume effects for studying the structural and thermodynamic properties of highly charged cylindrical polyelectrolytes. Several models of size and charge asymmetric mixtures of aqueous electrolytes at physiological concentrations are studied. Our results are in good agreement with Monte Carlo simulations. Our numerical calculations display significant differences in the ion density profiles for the different aqueous electrolyte models studied. However, similar results regarding the excess number of ions adsorbed to the B-DNA molecule are predicted by our theoretical approach for different aqueous electrolyte models. These findings suggest that ion counting experimental data should not be used alone to validate the performance of aqueous DNA-electrolyte models. PMID:25494770

  10. Asymmetric Gepner models (revisited)

    Energy Technology Data Exchange (ETDEWEB)

    Gato-Rivera, B. [NIKHEF Theory Group, Kruislaan 409, 1098 SJ Amsterdam (Netherlands)] [Instituto de Fisica Fundamental, CSIC, Serrano 123, Madrid 28006 (Spain); Schellekens, A.N., E-mail: t58@nikhef.n [NIKHEF Theory Group, Kruislaan 409, 1098 SJ Amsterdam (Netherlands)] [Instituto de Fisica Fundamental, CSIC, Serrano 123, Madrid 28006 (Spain)] [IMAPP, Radboud Universiteit, Nijmegen (Netherlands)

    2010-12-11

    We reconsider a class of heterotic string theories studied in 1989, based on tensor products of N=2 minimal models with asymmetric simple current invariants. We extend this analysis from (2,2) and (1,2) spectra to (0,2) spectra with SO(10) broken to the Standard Model. In the latter case the spectrum must contain fractionally charged particles. We find that in nearly all cases at least some of them are massless. However, we identify a large subclass where the fractional charges are at worst half-integer, and often vector-like. The number of families is very often reduced in comparison to the 1989 results, but there are no new tensor combinations yielding three families. All tensor combinations turn out to fall into two classes: those where the number of families is always divisible by three, and those where it is never divisible by three. We find an empirical rule to determine the class, which appears to extend beyond minimal N=2 tensor products. We observe that distributions of physical quantities such as the number of families, singlets and mirrors have an interesting tendency towards smaller values as the gauge groups approaches the Standard Model. We compare our results with an analogous class of free fermionic models. This displays similar features, but with less resolution. Finally we present a complete scan of the three family models based on the triply-exceptional combination (1,16{sup *},16{sup *},16{sup *}) identified originally by Gepner. We find 1220 distinct three family spectra in this case, forming 610 mirror pairs. About half of them have the gauge group SU(3)xSU(2){sub L}xSU(2){sub R}xU(1){sup 5}, the theoretical minimum, and many others are trinification models.

  11. Salt Effect on Osmotic Pressure of Polyelectrolyte Solutions: Simulation Study

    Directory of Open Access Journals (Sweden)

    Jan-Michael Y. Carrillo

    2014-07-01

    Full Text Available Abstract: We present results of the hybrid Monte Carlo/molecular dynamics simulations of the osmotic pressure of salt solutions of polyelectrolytes. In our simulations, we used a coarse-grained representation of polyelectrolyte chains, counterions and salt ions. During simulation runs, we alternate Monte Carlo and molecular dynamics simulation steps. Monte Carlo steps were used to perform small ion exchange between simulation box containing salt ions (salt reservoir and simulation box with polyelectrolyte chains, counterions and salt ions (polyelectrolyte solution. This allowed us to model Donnan equilibrium and partitioning of salt and counterions across membrane impermeable to polyelectrolyte chains. Our simulations have shown that the main contribution to the system osmotic pressure is due to salt ions and osmotically active counterions. The fraction of the condensed (osmotically inactive counterions first increases with decreases in the solution ionic strength then it saturates. The reduced value of the system osmotic coefficient is a universal function of the ratio of the concentration of osmotically active counterions and salt concentration in salt reservoir. Simulation results are in a very good agreement with osmotic pressure measurements in sodium polystyrene sulfonate, DNA, polyacrylic acid, sodium polyanetholesulfonic acid, polyvinylbenzoic acid, and polydiallyldimethylammonium chloride solutions.

  12. Short communication. Suitable growth stage to start irrigation with saline water to increase salt tolerance and decrease ion accumulation of Kochia scoparia (L. Schrad)

    Energy Technology Data Exchange (ETDEWEB)

    Salehi, M.; Kafi, M.

    2011-07-01

    Kochia scoparia L. Schard (common name: kochia) is a mesohalophyte, C4 plant. It has the potential of being an important fodder crop in arid and semi arid environments. In order to evaluate the effect of saline irrigation water on the seedling growth stage and to select the best growth stage to start using saline water, an experiment was conducted with seven different saline water treatments (1.5, 7, 14, 21, 28, 35 and 42 dS m{sup -}1) at four growth stages [after emergence (T1), 5 cm (T2), 10 cm (T3), and 15 cm (T4) of plant height]. Results showed that shoot dry biomass increased slightly up to 7 dS m{sup -}1 and after that decreased with increasing salinity. Salt tolerance of kochia increased at the T3 and T4 growth stages. Sodium content of the plant was increased by using high saline water. The adverse effect of salinity on the Na content of the plant was lower at the 10-15 cm growth stage than at earlier growth stages. Potassium content was not greatly affected by salinity. As conclusion, kochia is sensitive to saline irrigation at the earliest stages of growth, and the best plant height to start saline irrigation is between 10 and 15 cm. (Author) 18 refs.

  13. Electrophysical behavior of ion-conductive organic-inorganic polymer system based on aliphatic epoxy resin and salt of lithium perchlorate

    OpenAIRE

    Matkovska, Liubov; Iurzhenko, Maksym; Mamunya, Yevgen; Matkovska, Olga; Demchenko, Valeriy; Lebedev, Eugene; Boiteux, Gisele; Serghei, Anatoli

    2014-01-01

    Abstract In the present work, ion-conductive hybrid organic-inorganic polymers based on epoxy oligomer of diglycide aliphatic ester of polyethylene glycol (DEG) and lithium perchlorate (LiClO4) were synthesized. The effect of LiClO4 content on the electrophysical properties of epoxy polymers has been studied by differential scanning calorimetry (DSC) and broadband dielectric spectroscopy (BDS). The effect of LiClO4 content on the structure has been studied by wide-angle X-ray scattering (WAXS...

  14. Salt resistant crop plants

    KAUST Repository

    Roy, Stuart J.

    2014-04-01

    Soil salinity is a major constraint to agriculture. To improve salinity tolerance of crops, various traits can be incorporated, including ion exclusion, osmotic tolerance and tissue tolerance. We review the roles of a range of genes involved in salt tolerance traits. Different tissues and cells are adapted for specific and often diverse function, so it is important to express the genes in specific cell-types and to pyramid a range of traits. Modern biotechnology (marker- assisted selection or genetic engineering) needs to be increasingly used to introduce the correct combination of genes into elite crop cultivars. Importantly, the effects of introduced genes need to be evaluated in the field to determine their effect on salinity tolerance and yield improvement.

  15. Novel synthetic approach for 1, 4-dihydroxyanthraquinone and the development of its Lithiated salts as anode material for aqueous rechargeable Lithium-ion batteries

    KAUST Repository

    Gurukar, Suresh Shivappa

    2015-08-17

    The influence of organic electrode materials in the field of lithium ion battery is becoming a keen interest for the present generation scientists. Here we are reporting a novel method of synthesis of electrode material by the combination of sono-chemical and thermal methods. The advantages of organic active material towards lithium ion battery are of core interest of this study. The structural confirmations are by FT-IR, 1H NMR, MALDI-TOF Mass Spectroscopy and powder XRD data. The electrochemical properties of Lithiated-1,4-dihydroxyanthraquinone were studied using electrochemical-techniques such as Cyclic Voltammetry, Galvanostatic Cyclic Potential Limitation and Potentiostatic Electrochemical Impedance Spectroscopy. The satisfactory results towards stability of active species in the aqueous media, reasonable discharge capacity with 0.9 V average voltages and agreeable cycling performance during charge-discharge process with reproducibility are achieved. For the construction of the full cell, the anode material was coupled with the LiNi1/3Co1/3Mn1/3O2 as a cathode material.

  16. The deconfinement phase transition in asymmetric matter

    International Nuclear Information System (INIS)

    We study the phase transition of asymmetric hadronic matter to a quark-gluon plasma within the framework of a simple two-phase model. The analysis is performed in a system with two conserved charges (baryon number and isospin) using the stability conditions on the free energy, the conservation laws and Gibbs' criteria for phase equilibrium. The EOS is obtained in a separate description for the hadronic phase and for the quark-gluon plasma. For the hadrons, a relativistic mean-field model calibrated to the properties of nuclear matter is used, and a bag-model type EOS is used for the quarks and gluons. The model is applied to the deconfinement phase transition that may occur in matter created in ultra-relativistic collisions of heavy ions. Based on the two-dimensional coexistence surface (binodal), various phase separation scenarios and the Maxwell construction through the mixed phase are discussed. In the framework of the two-phase model the phase transition in asymmetric matter is continuous (second-order by Ehrenfest's definition) in contrast to the discontinuous (first-order) transition of symmetric systems. (orig.)

  17. Extraction of lanthanides ions (III) from aqueous solution by sodium salt of the N(4-amino-benzoate)-propyl-silica gel

    International Nuclear Information System (INIS)

    The silica gel 60 of specific superficial area 486 m2.g-1 was modified chemically with the ligand 4-amino benzoate of sodium in water-ethanol environment (l:L). The adsorptions of metallic ions were from water solutions at approximately 2 x 10-3 M of chloride of Pr(III), Nd(III), Eu(III) and Ho(III). In these experiments we could see that the system gets the equilibrium of adsorption rapidly and that the pH of the environment has a great influence on the process of adsorption, being that the number of metal mols adsorpted in the matrix varied between 10,00 and 17,00 x 10-5 mols. g-1 with a pH of approximately 5 for all the lanthanides, where the adsorption curves reach equilibrium. (author)

  18. Salt Tolerance of Desorption Electrospray Ionization (DESI)

    Energy Technology Data Exchange (ETDEWEB)

    Jackson, Ayanna U. [Purdue University; Talaty, Nari [Purdue University; Cooks, R G [Purdue University; Van Berkel, Gary J [ORNL

    2007-01-01

    Suppression of ion intensity in the presence of high salt matrices is common in most mass spectrometry ionization techniques. Desorption electrospray ionization (DESI) is an ionization method that exhibits salt tolerance, and this is investigated. DESI analysis was performed on three different drug mixtures in the presence of 0, 0.2, 2, 5, 10, and 20% NaCl:KCl weight by volume from seven different surfaces. At physiological concentrations individual drugs in each mixture were observed with each surface. Collision-induced dissociation (CID) was used to provide additional confirmation for select compounds. Multiple stage experiments, to MS5, were performed for select compounds. Even in the absence of added salt, the benzodiazepine containing mixture yielded sodium and potassium adducts of carbamazepine which masked the ions of interest. These adducts were eliminated by adding 0.1% 7M ammonium acetate to the standard methanol:water (1:1) spray solvent. Comparison of the salt tolerance of DESI with that of electrospray ionization (ESI) demonstrated much better signal/noise characteristics for DESI in this study. The salt tolerance of DESI was also studied by performing limit of detection and dynamic range experiments. Even at a salt concentration significantly above physiological concentrations, select surfaces were effective in providing spectra that allowed the ready identification of the compounds of interest. The already high salt tolerance of DESI can be optimized further by appropriate choices of surface and spray solution.

  19. Salt Acclimation of Cyanobacteria and Their Application in Biotechnology

    Directory of Open Access Journals (Sweden)

    Nadin Pade

    2014-12-01

    Full Text Available The long evolutionary history and photo-autotrophic lifestyle of cyanobacteria has allowed them to colonize almost all photic habitats on Earth, including environments with high or fluctuating salinity. Their basal salt acclimation strategy includes two principal reactions, the active export of ions and the accumulation of compatible solutes. Cyanobacterial salt acclimation has been characterized in much detail using selected model cyanobacteria, but their salt sensing and regulatory mechanisms are less well understood. Here, we briefly review recent advances in the identification of salt acclimation processes and the essential genes/proteins involved in acclimation to high salt. This knowledge is of increasing importance because the necessary mass cultivation of cyanobacteria for future use in biotechnology will be performed in sea water. In addition, cyanobacterial salt resistance genes also can be applied to improve the salt tolerance of salt sensitive organisms, such as crop plants.

  20. Solvent-assisted molten salt process: A new route to synthesise {alpha}-Fe{sub 2}O{sub 3}/C nanocomposite and its electrochemical performance in lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Hassan, Mohd Faiz, E-mail: mfh125@uow.edu.a [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); Department of Science Physics, University of Malaysia Terengganu, Kuala Terengganu 20522 (Malaysia); Rahman, M.M. [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); Guo, Zai Ping [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); School of Mechanical, Mechatronic and Materials Engineering, University of Wollongong, NSW 2522 (Australia); Chen, Zhi Xin [School of Mechanical, Mechatronic and Materials Engineering, University of Wollongong, NSW 2522 (Australia); Liu, Hua Kun [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia)

    2010-07-01

    Nanostructured {alpha}-Fe{sub 2}O{sub 3} was synthesised by a simple molten salt process using FeCl{sub 2}.4H{sub 2}O as a starting material and LiNO{sub 3}-LiOH.H{sub 2}O-H{sub 2}O{sub 2} as a eutectic mixture at 300 {sup o}C. To synthesise {alpha}-Fe{sub 2}O{sub 3}/C composite, both {alpha}-Fe{sub 2}O{sub 3} and malic acid were dispersed together in toluene, where malic acid was used as a carbon source. The morphology and microstructure of both compounds were confirmed by X-ray diffraction, Raman spectroscopy and transmission electron microscopy. Electrochemical testing, including constant current charge-discharge and cyclic voltammetry (CV), was carried out. The {alpha}-Fe{sub 2}O{sub 3}/C composite anode exhibited much better electrochemical performance than the bare {alpha}-Fe{sub 2}O{sub 3}. The discharge capacities of the composite were measured to be 2112 mAh g{sup -1} at C/2 after 100 cycles and 584 mAh g{sup -1} at 20 C after 10 cycles. The superior electrochemical performance of {alpha}-Fe{sub 2}O{sub 3}/C composite can be mainly attributed to the combined effects of the nanostructure, the carbon layering on the {alpha}-Fe{sub 2}O{sub 3} nanoparticles, and the porous ultra-fine carbon matrix, where the three factors would contribute to provide high electronic conductivity, reduce the traverse time of electrons and lithium-ions, and could also prevent high volume expansion of the anode film during cycling. Our results indicate that the prepared {alpha}-Fe{sub 2}O{sub 3}/C nanocomposite is a very promising anode material for Li-ion power batteries.

  1. Ion colliders

    International Nuclear Information System (INIS)

    Ion colliders are research tools for high-energy nuclear physics, and are used to test the theory of Quantum Chromo Dynamics (QCD). The collisions of fully stripped high-energy ions create matter of a temperature and density that existed only microseconds after the Big Bang. Ion colliders can reach higher densities and temperatures than fixed target experiments although at a much lower luminosity. The first ion collider was the CERN Intersecting Storage Ring (ISR), which collided light ions (77Asb1, 81Bou1). The BNL Relativistic Heavy Ion Collider (RHIC) is in operation since 2000 and has collided a number of species at numerous energies. The CERN Large Hadron Collider (LHC) started the heavy ion program in 2010. Table 1 shows all previous and the currently planned running modes for ISR, RHIC, and LHC. All three machines also collide protons, which are spin-polarized in RHIC. Ion colliders differ from proton or antiproton colliders in a number of ways: the preparation of the ions in the source and the pre-injector chain is limited by other effects than for protons; frequent changes in the collision energy and particle species, including asymmetric species, are typical; and the interaction of ions with each other and accelerator components is different from protons, which has implications for collision products, collimation, the beam dump, and intercepting instrumentation devices such a profile monitors. In the preparation for the collider use the charge state Z of the ions is successively increased to minimize the effects of space charge, intrabeam scattering (IBS), charge change effects (electron capture and stripping), and ion-impact desorption after beam loss. Low charge states reduce space charge, intrabeam scattering, and electron capture effects. High charge states reduce electron stripping, and make bending and acceleration more effective. Electron stripping at higher energies is generally more efficient. Table 2 shows the charge states and energies in the

  2. Physical chemistry and evolution of salt tolerance in halobacteria

    Science.gov (United States)

    Lanyi, J. K.

    1980-01-01

    The cellular constituents of extremely halophilic bacteria not only tolerate high salt concentration, but in many cases require it for optical functioning. The characteristics affected by salt include enzyme activity, stability, allosteric regulation, conformation and subunit association. The salt effects are of two major kinds: electrostatic shielding of negative charges by cations at low salt concentration, and hydrophobic stabilization by salting-out type salts at high salt concentration. The composition of halobacterial proteins shows an excess of acidic amino acids and a deficiency of nonpolar amino acids, which accounts for these effects. Since the cohesive forces are weaker and the repulsing forces are stronger in these proteins, preventing aggregation in salt, these structures are no longer suited for functioning in the absence of high salt concentrations. Unlike these nonspecific effects, ribosomes in halobacteria show marked preference for potassium over sodium ions. To ensure the proper intracellular ionic composition, powerful ion transport systems have evolved in the halobacteria, resulting in the extrusion of sodium ions and their replacement by potassium. It is likely that such membrane transport system for ionic movements is a necessary requisite for salt tolerance.

  3. Hydroxamic acids in asymmetric synthesis.

    Science.gov (United States)

    Li, Zhi; Yamamoto, Hisashi

    2013-02-19

    Metal-catalyzed stereoselective reactions are a central theme in organic chemistry research. In these reactions, the stereoselection is achieved predominantly by introducing chiral ligands at the metal catalyst's center. For decades, researchers have sought better chiral ligands for asymmetric catalysis and have made great progress. Nevertheless, to achieve optimal stereoselectivity and to catalyze new reactions, new chiral ligands are needed. Because of their high metal affinity, hydroxamic acids play major roles across a broad spectrum of fields from biochemistry to metal extraction. Dr. K. Barry Sharpless first revealed their potential as chiral ligands for asymmetric synthesis in 1977: He published the chiral vanadium-hydroxamic-acid-catalyzed, enantioselective epoxidation of allylic alcohols before his discovery of Sharpless asymmetric epoxidation, which uses the titanium-tartrate complex as the chiral reagent. However, researchers have reported few highly enantioselective reactions using metal-hydroxamic acid as catalysts since then. This Account summarizes our research on metal-catalyzed asymmetric epoxidation using hydroxamic acids as chiral ligands. We designed and synthesized a series of new hydroxamic acids, most notably the C2-symmetric bis-hydroxamic acid (BHA) family. V-BHA-catalyzed epoxidation of allylic and homoallylic alcohols achieved higher activity and stereoselectivity than Sharpless asymmetric epoxidation in many cases. Changing the metal species led to a series of unprecedented asymmetric epoxidation reactions, such as (i) single olefins and sulfides with Mo-BHA, (ii) homoallylic and bishomoallylic alcohols with Zr- and Hf-BHA, and (iii) N-alkenyl sulfonamides and N-sulfonyl imines with Hf-BHA. These reactions produce uniquely functionalized chiral epoxides with good yields and enantioselectivities. PMID:23157425

  4. Asymmetric counterpropagating fronts without flow.

    Science.gov (United States)

    Andrade-Silva, I; Clerc, M G; Odent, V

    2015-06-01

    Out-of-equilibrium systems exhibit domain walls between different states. These walls, depending on the type of connected states, can display rich spatiotemporal dynamics. In this Rapid Communication, we investigate the asymmetrical counterpropagation of fronts in an in-plane-switching cell filled with a nematic liquid crystal. Experimentally, we characterize the different front shapes and propagation speeds. These fronts present dissimilar elastic deformations that are responsible for their asymmetric speeds. Theoretically, using a phenomenological model, we describe the observed dynamics with fair agreement. PMID:26172647

  5. Incompressibility of asymmetric nuclear matter

    OpenAIRE

    Chen, Lie-Wen; Cai, Bao-Jun; Shen, Chun; Ko, Che Ming; Xu, Jun; Li, Bao-An(Department of Physics and Astronomy, Texas A&M University-Commerce, Commerce, TX, 75429-3011, USA)

    2009-01-01

    The incompressibility $K_sat(\\delta)$ of isospin asymmetric nuclear matter at its saturation density. Our results show that in the expansion of $K_sat(\\delta)$ in powers of isospin asymmetry $\\delta$, i.e., $K_sat(\\delta )$=K_{0}+K_{sat,2}\\delta^{2}+K_{sat,4}\\delta^{4}+O(\\delta^{6})$, the magnitude of the 4th-order K_{sat,4} parameter is generally small. The 2nd-order K_{sat,2} parameter thus essentially characterizes the isospin dependence of the incompressibility of asymmetric nuclear matte...

  6. Asymmetric Baxter-King filter

    OpenAIRE

    Buss, Ginters

    2011-01-01

    The paper proposes an extension of the symmetric Baxter-King band pass filter to an asymmetric Baxter-King filter. The optimal correction scheme of the ideal filter weights is the same as in the symmetric version, i.e, cut the ideal filter at the appropriate length and add a constant to all filter weights to ensure zero weight on zero frequency. Since the symmetric Baxter-King filter is unable to extract the desired signal at the very ends of the series, the extension to an asymmetric filter...

  7. Forces between asymmetric polymer brushes

    OpenAIRE

    Shim, D.F.K.; Cates, M. E.

    1990-01-01

    We study the equilibrium compression of asymmetric polymer brushes grafted on flat plates, under athermal and theta solvent conditions, using a lattice self-consistent field (SCF) approach. We find that the separation d between two plates coated asymmetrically with brushes of type 1 and 2, as a function of the force F, obeys the "bisection rule", d(F) = (d1(F) + d 2(F)) /2 where d1(F)and d 2(F) are the corresponding separations for the symmetric brushes of type 1 and 2 respectively.The bisect...

  8. Research on asymmetric "Jerusalem" unit

    Institute of Scientific and Technical Information of China (English)

    Jun Lu; Jianbo Wang

    2009-01-01

    An asymmetric Jerusalem unit and the frequency selective surface(FSS)structure composed of such units are designed.The transmittance of the designed FSS structure is calculated by mode-matching method and compared with the test results.The comparison results show that the FSS center frequency of the asymmetric structure unit drifts little with the variation of the incident angles of the electromagnetic waves and keeps relatively stable.The research offers a new choice for the application of FSS under the large scanning angle of electromagnetic waves.

  9. Numerical modeling of deformation in salt basins: Technical report

    International Nuclear Information System (INIS)

    The report describes the dominant physical mechanisms and the material properties influence in the formation of natural salt deformation features within a salt basin. Numerical analysis techniques include one-dimensional, closed-form analytical solutions; one-dimensional analytical solutions employing a numerical propagator matrix technique; and a two-dimensional, finite-element, viscoplastic numerical code (MANTLE). The published works of earlier investigators were reviewed, along with conventional applications of the one-dimensional, closed-form solutions. Earlier work was extended to more complex multilayered, thin interbed systems, using a numerical propagator matrix. Nonlinear salt properties and two-dimensional mechanisms were modeled, including horizontal tectonic strain, predeposition-of-salt basement faulting, and postdeposition-of-salt basement faulting, with vertical shear stress produced in the overlying salt. The study concludes that the conventional analyses using assumed effective viscosities for salt and density-inversion mechanics are incorrect, first-order or major perturbations in a bedded salt formation require the application of shear stress to initiate the appropriate growth rate, a condition of postdeposition basement faulting is the probable mechanism to initiate such shear stress, and interbed and internal salt fabric (second-order and higher) deformation characteristics can be strongly asymmetric to the major deformation surfaces in the region of basement faulting/shear stress location. 28 refs., 70 figs., 3 tabs

  10. SINGLE IONIC CONDUCTION OF POLYSILOXANE CONTAINING PROPYLENE CARBONATE GROUP AND LITHIUM POLYMERIC SALTS

    Institute of Scientific and Technical Information of China (English)

    CHEN Xiwen; FANG Shibi; HAO Ning; JIANG Yingyan

    1996-01-01

    The polysiloxane containing propylene carbonate side group and several lithium polymeric salts were synthesized. The structure were confirmed by IR, NMR and XPS. The blending systems of polysiloxane containing propylene carbonate group with different lithium polymeric salts were studied by ion conductivity, XPS and DSC. Different lithium polymeric salts in the blending system lead to conductivity arranged in the following sequence:poly(lithium ethylenebenzene sulfonate methylsiloxane) > poly(lithium propionate methylsiloxane) > poly(lithium propylsulfonate methylsiloxane) > poly(lithium styrenesulfonate).In the blending system the best single ion conductivity was close to 10-5 Scm-1 at room temperature. XPS showed that at low lithium salt concentration the conductivity increased with the increasing content of lithium salt, in consequence of the increase of free ion and solvent separated ion pair. At high lithium salt concentration the free ion was absent and the solvent-separated ion pair functioned as carrier.

  11. The structure and IR signatures of the arginine-glutamate salt bridge. Insights from the classical MD simulations

    Energy Technology Data Exchange (ETDEWEB)

    Vener, M. V., E-mail: mikhail.vener@gmail.com [Mendeleev University of Chemical Technology, Moscow (Russian Federation); Odinokov, A. V. [Photochemistry Center of the Russian Academy of Sciences, Moscow (Russian Federation); Wehmeyer, C. [Free University, Berlin (Germany); Sebastiani, D. [Martin-Luther-Universität Halle-Wittenberg, Halle (Germany)

    2015-06-07

    Salt bridges and ionic interactions play an important role in protein stability, protein-protein interactions, and protein folding. Here, we provide the classical MD simulations of the structure and IR signatures of the arginine (Arg)–glutamate (Glu) salt bridge. The Arg-Glu model is based on the infinite polyalanine antiparallel two-stranded β-sheet structure. The 1 μs NPT simulations show that it preferably exists as a salt bridge (a contact ion pair). Bidentate (the end-on and side-on structures) and monodentate (the backside structure) configurations are localized [Donald et al., Proteins 79, 898–915 (2011)]. These structures are stabilized by the short {sup +}N–H⋯O{sup −} bonds. Their relative stability depends on a force field used in the MD simulations. The side-on structure is the most stable in terms of the OPLS-AA force field. If AMBER ff99SB-ILDN is used, the backside structure is the most stable. Compared with experimental data, simulations using the OPLS all-atom (OPLS-AA) force field describe the stability of the salt bridge structures quite realistically. It decreases in the following order: side-on > end-on > backside. The most stable side-on structure lives several nanoseconds. The less stable backside structure exists a few tenth of a nanosecond. Several short-living species (solvent shared, completely separately solvated ionic groups ion pairs, etc.) are also localized. Their lifetime is a few tens of picoseconds or less. Conformational flexibility of amino acids forming the salt bridge is investigated. The spectral signature of the Arg-Glu salt bridge is the IR-intensive band around 2200 cm{sup −1}. It is caused by the asymmetric stretching vibrations of the {sup +}N–H⋯O{sup −} fragment. Result of the present paper suggests that infrared spectroscopy in the 2000–2800 frequency region may be a rapid and quantitative method for the study of salt bridges in peptides and ionic interactions between proteins. This region is

  12. The structure and IR signatures of the arginine-glutamate salt bridge. Insights from the classical MD simulations

    International Nuclear Information System (INIS)

    Salt bridges and ionic interactions play an important role in protein stability, protein-protein interactions, and protein folding. Here, we provide the classical MD simulations of the structure and IR signatures of the arginine (Arg)–glutamate (Glu) salt bridge. The Arg-Glu model is based on the infinite polyalanine antiparallel two-stranded β-sheet structure. The 1 μs NPT simulations show that it preferably exists as a salt bridge (a contact ion pair). Bidentate (the end-on and side-on structures) and monodentate (the backside structure) configurations are localized [Donald et al., Proteins 79, 898–915 (2011)]. These structures are stabilized by the short +N–H⋯O− bonds. Their relative stability depends on a force field used in the MD simulations. The side-on structure is the most stable in terms of the OPLS-AA force field. If AMBER ff99SB-ILDN is used, the backside structure is the most stable. Compared with experimental data, simulations using the OPLS all-atom (OPLS-AA) force field describe the stability of the salt bridge structures quite realistically. It decreases in the following order: side-on > end-on > backside. The most stable side-on structure lives several nanoseconds. The less stable backside structure exists a few tenth of a nanosecond. Several short-living species (solvent shared, completely separately solvated ionic groups ion pairs, etc.) are also localized. Their lifetime is a few tens of picoseconds or less. Conformational flexibility of amino acids forming the salt bridge is investigated. The spectral signature of the Arg-Glu salt bridge is the IR-intensive band around 2200 cm−1. It is caused by the asymmetric stretching vibrations of the +N–H⋯O− fragment. Result of the present paper suggests that infrared spectroscopy in the 2000–2800 frequency region may be a rapid and quantitative method for the study of salt bridges in peptides and ionic interactions between proteins. This region is usually not considered in

  13. Detection, identification, and occurrence of thiotetronic acids in drinking water from underground sources by electrospray ionization-high field asymmetric waveform ion mobility spectrometry-quadrupole time-of-flight-mass spectrometry.

    Science.gov (United States)

    Lyczko, Jadwiga; Beach, Daniel; Gabryelski, Wojciech

    2015-10-01

    This paper demonstrates that electrospray ionization (ESI) with differential ion mobility spectroscopy (FAIMS) and "soft" mass spectrometry (MS) provide unique analytical capabilities that led to the discovery of sulfur-containing polar congeners of thiotetronic acid (TA) in drinking water from underground sources in Canada and the United States. Polar TAs accumulate in underground aquifers and appear to be the most abundant class of organic compounds in bottled water but cannot be detected by conventional mass spectrometry methods. We show that normally stable TAs are converted into very reactive ions in ESI which have to be analyzed using special conditions in ESI-FAIMS-MS to avoid extensive dissociation and ion/molecule reactions. De novo identification of 10 TAs was accomplished by the comparative tandem mass spectrometry analysis of authentic TA derivatives from groundwater samples and synthetic TA analogues prepared for this study. We present highlights of gas phase ion chemistry of polar TAs to explain their unique properties and reactivity. TA derivatives were originally isolated from soil bacteria and are of interest in the pharmaceutical industry due to their potent activity against a broad spectrum of pathogenic bacteria and negligible toxicity to mammals. We suspect that TAs are natural disinfection agents protecting groundwater from bacterial contamination, but these compound undergo modifications or decompose during an ozonation water treatment. PMID:26340067

  14. Novel FinFET Device Using Asymmetric Doping

    DEFF Research Database (Denmark)

    Moradi, Farshad

    2012-01-01

    In this paper, a new technique is proposed to improve the device characteristics by introducing asymmetric doping at the source and the drain of the conventional FinFET. Specifically, the proposed device exhibits 9X increase of the Ion/Ioff ratio and 3X improved DIBL compared to conventional symm...... symmetric FinFET devices. We note a reduction in sub-threshold swing (SS) of 16% with 7% Ion degradation. The proposed FinFETs can be utilized in SRAM cells and logic circuits to improve their functionality at ultra-scaled technologies....

  15. Pyroelectricity and Asymmetric Thermal Vibrations of Atoms in Minerals

    Science.gov (United States)

    Kihara, Kuniaki; Okudera, Hiroki

    A structural approach was attempted to estimate rigid ion contributions to pyroelectric coefficients, employing atomic position vectors determined in the least-squares refinement of a polar mineral, cancrinite. The two sets of positions, obtained from the centers of gravity (centroids) and modes of asymmetric probability density functions (pdf) of atoms, were applied to calculate electric polarizations, whose temperature derivatives may correspond to the rigid ion contributions to the pyroelectric coefficient, γ(σ), normally measured under the condition of constant stresses and to the secondary pyroelectric coefficients, γ(2), respectively. The primary pyroelectric coefficient γ(ε) was given as the difference γ(σ)-γ(2).

  16. Salt effects in electromembrane extraction.

    Science.gov (United States)

    Seip, Knut Fredrik; Jensen, Henrik; Kieu, Thanh Elisabeth; Gjelstad, Astrid; Pedersen-Bjergaard, Stig

    2014-06-20

    Electromembrane extraction (EME) was performed on samples containing substantial amounts of NaCl to investigate how the presence of salts affected the recovery, repeatability, and membrane current in the extraction system. A group of 17 non-polar basic drugs with various physical chemical properties were used as model analytes. When EME was performed in a hollow fiber setup with a supported liquid membrane (SLM) comprised of 2-nitrophenyl octyl ether (NPOE), a substantial reduction in recovery was seen for eight of the substances when 2.5% (w/v) NaCl was present. No correlation between this loss and the physical chemical properties of these substances was seen. The recovery loss was hypothesized to be caused by ion pairing in the SLM, and a mathematical model for the extraction recovery in the presence of salts was made according to the experimental observations. Some variations to the EME system reduced this recovery loss, such as changing the SLM solvent from NPOE to 6-undecanone, or by using a different EME setup with more favorable volume ratios. This was in line with the ion pairing hypothesis and the mathematical model. This thorough investigation of how salts affect EME improves the theoretical understanding of the extraction process, and can contribute to the future development and optimization of the technique. PMID:24792700

  17. Solid-state electrochromic devices based on poly(trimethylene carbonate) and lithium salts

    International Nuclear Information System (INIS)

    The application of solid polymer electrolytes as dual-function electrolyte/adhesive components in electrochromic devices and the preliminary characterization of the resulting prototype displays is described in this paper. An asymmetric device configuration, represented schematically as glass/ZnO:Ga2O3/WO3/polymer electrolyte/ZnO:Ga2O3/glass, was chosen. Electrolytes with compositions of n between 3 and 10, where n represents the molar ratio of poly(trimethylene carbonate), p(TMC), ((C=O)OCH2CH2CH2O), units per guest lithium ion, were prepared by solvent casting. The electrochromic switching performance was characterized as a function of salt type and salt concentration. The average transmittance in the visible region of the spectrum was above 63% for all the bleached samples characterized. After coloration the structures assembled with both p(TMC)nLiClO4 and p(TMC)nLiBF4 presented an average transmittance in the visible wavelength region above 39%

  18. Solid-state electrochromic devices based on poly(trimethylene carbonate) and lithium salts

    Energy Technology Data Exchange (ETDEWEB)

    Barbosa, P.C. [Centro de Quimica, Universidade do Minho, Gualtar, 4710-057 Braga (Portugal); Silva, M.M. [Centro de Quimica, Universidade do Minho, Gualtar, 4710-057 Braga (Portugal)], E-mail: nini@quimica.uminho.pt; Smith, M.J. [Centro de Quimica, Universidade do Minho, Gualtar, 4710-057 Braga (Portugal); Goncalves, A.; Fortunato, E. [Centro de Investigacao de Materiais, Universidade Nova de Lisboa, Campus da FCT 2829-516 Caparica (Portugal)

    2008-02-15

    The application of solid polymer electrolytes as dual-function electrolyte/adhesive components in electrochromic devices and the preliminary characterization of the resulting prototype displays is described in this paper. An asymmetric device configuration, represented schematically as glass/ZnO:Ga{sub 2}O{sub 3}/WO{sub 3}/polymer electrolyte/ZnO:Ga{sub 2}O{sub 3}/glass, was chosen. Electrolytes with compositions of n between 3 and 10, where n represents the molar ratio of poly(trimethylene carbonate), p(TMC), ((C=O)OCH{sub 2}CH{sub 2}CH{sub 2}O), units per guest lithium ion, were prepared by solvent casting. The electrochromic switching performance was characterized as a function of salt type and salt concentration. The average transmittance in the visible region of the spectrum was above 63% for all the bleached samples characterized. After coloration the structures assembled with both p(TMC){sub n}LiClO{sub 4} and p(TMC){sub n}LiBF{sub 4} presented an average transmittance in the visible wavelength region above 39%.

  19. The cobalt(II salt of the azo dye Orange G

    Directory of Open Access Journals (Sweden)

    Maurice O. Okoth

    2010-10-01

    Full Text Available Crystallizing the cobalt(II salt of the azo dye Orange G from water was found to give the solvent-separated ion-pair species hexaaquacobalt(II 7-oxo-8-(2-phenylhydrazin-1-ylidene-7,8-dihydronaphthalene-1,3-disulfonate tetrahydrate, [Co(H2O6](C16H10N2O7S2·4H2O. The asymmetric unit of the cobalt(II salt contains three independent octahedral [Co(OH26]2+ cations, three azo anions, all with similar configurations, and 12 uncoordinated water molecules. The structure is closely related to that of one of the known magnesium analogues. Both structures have Z′ = 3, feature nearly planar azo anions [maximum displacement of azo-N atoms from the plane of the phenyl ring = 0.058 (7 Å] in their hydrazone tautomeric form, form layer structures with hydrophilic and hydrophobic layers alternating along the b-axis direction, and are stabilized by an extensive network of hydrogen bonds..

  20. Salt: a sacred substance.

    Science.gov (United States)

    De Santo, N G; Bisaccia, C; De Santo, R M; De Santo, L S; Petrelli, L; Gallo, L; Cirillo, M; Capasso, G

    1997-11-01

    Salt is the last relic of the ocean where life was born. Its presence has influenced the whole gamut of history and its name is linked to hundred of geographical locations. Its importance for nutrition is supported by the discovery of Aeneolithic salt cellars. Salt cellars and pyramids of salt have been included in paintings and other works of art. In Japan where salt was and still is obtained from the sea, a salt culture has developed that can be traced in the rituals of everyday life, including meal preparation, sports, and Shinto ceremonies. PMID:9350697

  1. JET and COMPASS asymmetrical disruptions

    Czech Academy of Sciences Publication Activity Database

    Gerasimov, S.N.; Abreu, P.; Baruzzo, M.; Drozdov, V.; Dvornova, A.; Havlíček, Josef; Hender, T.C.; Hronová-Bilyková, Olena; Kruezi, U.; Li, X.; Markovič, Tomáš; Pánek, Radomír; Rubinacci, G.; Tsalas, M.; Ventre, S.; Villone, F.; Zakharov, L.E.

    2015-01-01

    Roč. 55, č. 11 (2015), s. 113006-113006. ISSN 0029-5515 R&D Projects: GA MŠk(CZ) LM2011021 Institutional support: RVO:61389021 Keywords : tokamak * asymmetrical disruption * JET * COMPASS Subject RIV: BL - Plasma and Gas Discharge Physics Impact factor: 3.062, year: 2014

  2. Synthesis of Asymmetric Propanetriol Analogues

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    From natural tartaric acid, (R)-2-benzyloxy-3-(2-tetrahydropyranyloxy) propanol 3 was designed and synthesized, and (R)-2-benzyloxy-3-(4-methoxybenzyloxy) propanol 7 was prepared in a new method. They can be used as chiral synthons of lysophosphatidic acid and other compounds with asymmetric propanetriol backbone.

  3. Asymmetrical Switch Costs in Children

    Science.gov (United States)

    Ellefson, Michelle R.; Shapiron, Laura R.; Chater, Nick

    2006-01-01

    Switching between tasks produces decreases in performance as compared to repeating the same task. Asymmetrical switch costs occur when switching between two tasks of unequal difficulty. This asymmetry occurs because the cost is greater when switching to the less difficult task than when switching to the more difficult task. Various theories about…

  4. Asymmetric Synthesis via Chiral Aziridines

    DEFF Research Database (Denmark)

    Tanner, David Ackland; Harden, Adrian; Wyatt, Paul; Andersson, Pher G.; Johansson, Fredrik

    1996-01-01

    A series of chiral bis(aziridines) has been synthesised and evaluated as chelating ligands for a variety of asymmetric transformations mediated by metals [Os (dihydroxylation), Pd (allylic alkylation) Cu (cyclopropanation and aziridination, Li (1,2-addition of organolithiums to imines)]. In the...

  5. Selfhealing of asymmetric Bessel-like modes

    DEFF Research Database (Denmark)

    Israelsen, Stine Møller; Rishøj, Lars Søgaard; Rottwitt, Karsten

    2014-01-01

    We numerically investigate asymmetric Bessel-like modes in an aircladding fiber. The selfhealing ability of asymmetric Bessel-like modes is demonstrated and quantified including the angular dependency of this ability.......We numerically investigate asymmetric Bessel-like modes in an aircladding fiber. The selfhealing ability of asymmetric Bessel-like modes is demonstrated and quantified including the angular dependency of this ability....

  6. Salt effects in electromembrane extraction

    DEFF Research Database (Denmark)

    Seip, Knut Fredrik; Jensen, Henrik; Kieu, Thanh Elisabeth;

    2014-01-01

    Electromembrane extraction (EME) was performed on samples containing substantial amounts of NaCl to investigate how the presence of salts affected the recovery, repeatability, and membrane current in the extraction system. A group of 17 non-polar basic drugs with various physical chemical...... properties were used as model analytes. When EME was performed in a hollow fiber setup with a supported liquid membrane (SLM) comprised of 2-nitrophenyl octyl ether (NPOE), a substantial reduction in recovery was seen for eight of the substances when 2.5% (w/v) NaCl was present. No correlation between...... this loss and the physical chemical properties of these substances was seen. The recovery loss was hypothesized to be caused by ion pairing in the SLM, and a mathematical model for the extraction recovery in the presence of salts was made according to the experimental observations. Some variations...

  7. The Design of Reactions, Catalysts and Materials with Aromatic Ions

    Science.gov (United States)

    Bandar, Jeffrey Scott

    (dialkylamino)cyclopropenimine catalyst to promote asymmetric Mannich reactions of glycinate imines and N -Boc-aldimines is described in Chapter 4. The products of this transformation are optically enriched diamino acid derivatives, an important motif widely utilized in medicinal and synthetic chemistry. Importantly, unlike existing methods, our technology promotes reactions between tert-butyl glycinate and aliphatic N-Boc-aldimine substrates. A preparative-scale reaction is demonstrated and derivatization of its product to several valuable chiral compounds is shown. Chapter 5 describes the use of tris(dialkylamino)cyclopropenium (TDAC) ions as a new class of onium-like catalyst. A simple TDAC chloride salt is prepared on a 75-gram scale and its use as a phase transfer catalyst for a variety of reactions is demonstrated. This same salt is also utilized as an epoxide opening catalyst for a variety of transformations, including the fixation of carbon dioxide. Chapter 6 briefly highlights several continued applications of the chemistry advanced throughout this thesis. First, the work of other members of the Lambert Group toward the continued development of cyclopropenimine chemistry is described. Second, a broad initiative between the Lambert and Campos Groups at Columbia University focused on the synthesis and application of TDAC-based polymers is introduced. Lastly, the identification of a previously unknown equilibrium between fulvenes and imines/aldehydes in the context of a new mode of catalysis is presented.

  8. Hybrid materials from organic polymers and inorganic salts

    OpenAIRE

    Köberle, Peter; Laschewsky, André

    2008-01-01

    The prepaparation of amorphous, homogeneous blends of zwitterionic polymers and transition metal salts was investigated. Homogeneous miscibility was achieved in many cases up to equimolar amounts of salt, depending on the anion and cation chosen. Various analytical techniques point to a solid state solution of the inorganic ions in the polymer matrix.

  9. Molten salt electrolyte separator

    Science.gov (United States)

    Kaun, Thomas D.

    1996-01-01

    A molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication.

  10. Measurement of Concentrations of Magnesium Ion by Masking Method in Presence of the Interference Lithium Ion in Salt Water System%水盐体系中有干扰Li+离子存在下测定Mg2+浓度的掩蔽法研究

    Institute of Scientific and Technical Information of China (English)

    李红霞; 姚燕; 曾德文

    2012-01-01

    There are abundant lithium ions in salt water system,which lead to serious interference in magnesium measurement by the complexometric titration method with EDTA, making titration results on the high side. In this paper,the authors choose n-butanol and absolute ethylalcohol with the volume ratio of 1:9 as masking agent. What' s more,we discuss the suitable quantity of the mixed alcohol added to the sample under the different Li+/Mg2+ mole ratio, concentrations and sampling volumes. Eventually, this paper indicates that the added quantity of the mixed alcohol has a bigger connection with Li+/Mg2+ mole ratios,but has no obvious connection with the concentrations and the sampling volumes,under the same Li+/Mg2+ mole ratio, the added quantity of the mixed alcohol has a suitable range. The measurement errors for this analytical method could be within 0. 3%. This paper is important to improve reliability and accuracy of the phase chemistry experiment containing lithium ion and magnesium ion in salt water system.%在水盐体系中,大量Li+的存在,对EDTA络合滴定法测镁有严重的干扰,使滴定结果偏高.采用体积比为1∶9的正丁醇与无水乙醇作掩蔽剂,探究其在不同Li+/Mg2+摩尔比、不同浓度、不同取样量下的适宜加入量,得出混合醇的加入量与Li+/Mg2+摩尔比有较大关系,与溶液浓度、取样重的多少均无明显关系;同时指出在同一Li+/Mg2+摩尔比下混合醇的加入量有个适宜的范围.该方法的相对误差不大于0.3%.对提高含Li+和Mg2+的水盐体系相化学实验研究的可靠性和精度具有重要意义.

  11. Fluorescent carbon dot–molecular salt hydrogels

    OpenAIRE

    Cayuela, Angelina; Kennedy, Stuart R.; Soriano, Laura; Jones, Christopher D.; Valcárcel, M.; Steed, Jonathan W.

    2015-01-01

    The incorporation of functionalised carbon nanodots within a novel low molecular weight salt hydrogel derived from 5-aminosalicylic acid is reported. The carbon dots result in markedly enhanced gelation properties, while inclusion within the hydrophobic gel results in a dramatic fluorescence enhancement for the carbon nanomaterials. The resulting hybrid CD gels exhibit a useful sensor response for heavy metal ions, particularly Pb2+.

  12. Salt preferences of honey bee water foragers.

    Science.gov (United States)

    Lau, Pierre W; Nieh, James C

    2016-03-15

    The importance of dietary salt may explain why bees are often observed collecting brackish water, a habit that may expose them to harmful xenobiotics. However, the individual salt preferences of water-collecting bees were not known. We measured the proboscis extension reflex (PER) response of Apis mellifera water foragers to 0-10% w/w solutions of Na, Mg and K, ions that provide essential nutrients. We also tested phosphate, which can deter foraging. Bees exhibited significant preferences, with the most PER responses for 1.5-3% Na and 1.5% Mg. However, K and phosphate were largely aversive and elicited PER responses only for the lowest concentrations, suggesting a way to deter bees from visiting contaminated water. We then analyzed the salt content of water sources that bees collected in urban and semi-urban environments. Bees collected water with a wide range of salt concentrations, but most collected water sources had relatively low salt concentrations, with the exception of seawater and swimming pools, which had >0.6% Na. The high levels of PER responsiveness elicited by 1.5-3% Na may explain why bees are willing to collect such salty water. Interestingly, bees exhibited high individual variation in salt preferences: individual identity accounted for 32% of variation in PER responses. Salt specialization may therefore occur in water foragers. PMID:26823100

  13. Nano-LiNiO2 as cathode material for lithium ion battery synthesized by molten salt method%熔融盐法合成锂离子电池正极材料纳米LiNiO2

    Institute of Scientific and Technical Information of China (English)

    白莹; 王蓓; 张伟风

    2011-01-01

    采用熔融盐法,在较低的温度和较短的时间制备了符合理论化学计量比的纳米LiNiO2.研究表明,经过空气中的低温预烧,可以使制备的纯相纳米LiNiO2具有更加优良的结晶性能和更佳的电化学特性.添加预烧步骤前后所得最终产物的初始容量分别为151和148 mAh·g-1,经过100周的循环,容量衰减到55和118 mAh·g-1,容量保持率分别为36.4%和79.7%.原因在于预烧后再进行煅烧降低了阳离子无序度,减少了混杂在Li层中的Ni离子,从而有利于Li离子的扩散,优化了电化学性能.%Molten salt method is applied to synthesis stoichiometric nano-LiNiO2 in rather low temperature and short time. Our results indicate that in the process of preheating the better-crystallized LiNiO2 powder with better electrochemical performances can be produced. The final samples before and after preheating exhibit the initial discharge capacities of 151 and 148 mAh·g-1 respectively. After 100 cycles, they decay to only 55 and 118 mAh·g-1 , with capacity retentions being 36. 4% and 79. 7% respectively. The lowered cation disordering is thought to be favorable for the diffusion of lithium ions, by which the enhanced electrochemial properties can be explained.

  14. Salt splitting using ceramic membranes

    Energy Technology Data Exchange (ETDEWEB)

    Kurath, D.E. [Pacific Northwest National Lab., Richland, WA (United States)

    1997-10-01

    Many radioactive aqueous wastes in the DOE complex have high concentrations of sodium that can negatively affect waste treatment and disposal operations. Sodium can decrease the durability of waste forms such as glass and is the primary contributor to large disposal volumes. Waste treatment processes such as cesium ion exchange, sludge washing, and calcination are made less efficient and more expensive because of the high sodium concentrations. Pacific Northwest National Laboratory (PNNL) and Ceramatec Inc. (Salt Lake City UT) are developing an electrochemical salt splitting process based on inorganic ceramic sodium (Na), super-ionic conductor (NaSICON) membranes that shows promise for mitigating the impact of sodium. In this process, the waste is added to the anode compartment, and an electrical potential is applied to the cell. This drives sodium ions through the membrane, but the membrane rejects most other cations (e.g., Sr{sup +2}, Cs{sup +}). The charge balance in the anode compartment is maintained by generating H{sup +} from the electrolysis of water. The charge balance in the cathode is maintained by generating OH{sup {minus}}, either from the electrolysis of water or from oxygen and water using an oxygen cathode. The normal gaseous products of the electrolysis of water are oxygen at the anode and hydrogen at the cathode. Potentially flammable gas mixtures can be prevented by providing adequate volumes of a sweep gas, using an alternative reductant or destruction of the hydrogen as it is generated. As H{sup +} is generated in the anode compartment, the pH drops. The process may be operated with either an alkaline (pH>12) or an acidic anolyte (pH <1). The benefits of salt splitting using ceramic membranes are (1) waste volume reduction and reduced chemical procurement costs by recycling of NaOH; and (2) direct reduction of sodium in process streams, which enhances subsequent operations such as cesium ion exchange, calcination, and vitrification.

  15. Cyclodextrins in Asymmetric and Stereospecific Synthesis

    Directory of Open Access Journals (Sweden)

    Fliur Macaev

    2015-09-01

    Full Text Available Since their discovery, cyclodextrins have widely been used as green and easily available alternatives to promoters or catalysts of different chemical reactions in water. This review covers the research and application of cyclodextrins and their derivatives in asymmetric and stereospecific syntheses, with their division into three main groups: (1 cyclodextrins promoting asymmetric and stereospecific catalysis in water; (2 cyclodextrins’ complexes with transition metals as asymmetric and stereospecific catalysts; and (3 cyclodextrins’ non-metallic derivatives as asymmetric and stereospecific catalysts. The scope of this review is to systematize existing information on the contribution of cyclodextrins to asymmetric and stereospecific synthesis and, thus, to facilitate further development in this direction.

  16. Bis(toluene)chromium(I) [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]thiadiazolo[3,4-b]pyrazinidyl: new heterospin (S1 = S2 = ½) radical-ion salts.

    Science.gov (United States)

    Semenov, Nikolay A; Pushkarevsky, Nikolay A; Suturina, Elizaveta A; Chulanova, Elena A; Kuratieva, Natalia V; Bogomyakov, Artem S; Irtegova, Irina G; Vasilieva, Nadezhda V; Konstantinova, Lidia S; Gritsan, Nina P; Rakitin, Oleg A; Ovcharenko, Victor I; Konchenko, Sergey N; Zibarev, Andrey V

    2013-06-01

    Bis(toluene)chromium(0), Cr(0)(η(6)-C7H8)2 (3), readily reduced [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazole (1) and [1,2,5]thiadiazolo[3,4-b]pyrazine (2) in a tetrahydrofuran solvent with the formation of heterospin, S1 = S2 = ½, radical-ion salts [3](+)[1](-) (4) and [3](+)[2](-) (5) isolated in high yields. The salts 4 and 5 were characterized by single-crystal X-ray diffraction (XRD), solution and solid-state electron paramagnetic resonance, and magnetic susceptibility measurements in the temperature range 2-300 K. Despite the formal similarity of the salts, their crystal structures were very different and, in contrast to 4, in 5 anions were disordered. For the XRD structures of the salts, parameters of the Heisenberg spin Hamiltonian were calculated using the CASSCF/NEVPT2 and broken-symmetry density functional theory approaches, and the complex magnetic motifs featuring the dominance of antiferromagnetic (AF) interactions were revealed. The experimental χT temperature dependences of the salts were simulated using the Van Vleck formula and a diagonalization of the matrix of the Heisenberg spin Hamiltonian for the clusters of 12 paramagnetic species with periodic boundary conditions. According to the calculations and χT temperature dependence simulation, a simplified magnetic model can be suggested for the salt 4 with AF interactions between the anions ([1](-)···[1](-), J1 = -5.77 cm(-1)) and anions and cations ([1](-)···[3](+), J2 = -0.84 cm(-1)). The magnetic structure of the salt 5 is much more complex and can be characterized by AF interactions between the anions, [2](-)···[2](-), and by both AF and ferromagnetic (FM) interactions between the anions and cations, [2](-)···[3](+). The contribution from FM interactions to the magnetic properties of the salt 5 is in qualitative agreement with the positive value of the Weiss constant Θ (0.4 K), whereas for salt 4, the constant is negative (-7.1 K). PMID:23687983

  17. Stable walking with asymmetric legs

    International Nuclear Information System (INIS)

    Asymmetric leg function is often an undesired side-effect in artificial legged systems and may reflect functional deficits or variations in the mechanical construction. It can also be found in legged locomotion in humans and animals such as after an accident or in specific gait patterns. So far, it is not clear to what extent differences in the leg function of contralateral limbs can be tolerated during walking or running. Here, we address this issue using a bipedal spring-mass model for simulating walking with compliant legs. With the help of the model, we show that considerable differences between contralateral legs can be tolerated and may even provide advantages to the robustness of the system dynamics. A better understanding of the mechanisms and potential benefits of asymmetric leg operation may help to guide the development of artificial limbs or the design novel therapeutic concepts and rehabilitation strategies.

  18. Asymmetrically coupled directed percolation systems

    OpenAIRE

    Noh, Jae Dong; Park, Hyunggyu

    2005-01-01

    We introduce a dynamical model of coupled directed percolation systems with two particle species. The two species $A$ and $B$ are coupled asymmetrically in that $A$ particles branch $B$ particles whereas $B$ particles prey on $A$ particles. This model may describe epidemic spreading controlled by reactive immunization agents. We study nonequilibrium phase transitions with focused attention to the multicritical point where both species undergo the absorbing phase transition simultaneously. In ...

  19. Asymmetric information and macroeconomic dynamics

    Science.gov (United States)

    Hawkins, Raymond J.; Aoki, Masanao; Roy Frieden, B.

    2010-09-01

    We show how macroeconomic dynamics can be derived from asymmetric information. As an illustration of the utility of this approach we derive the equilibrium density, non-equilibrium densities and the equation of motion for the response to a demand shock for productivity in a simple economy. Novel consequences of this approach include a natural incorporation of time dependence into macroeconomics and a common information-theoretic basis for economics and other fields seeking to link micro-dynamics and macro-observables.

  20. Entrepreneurship, Asymmetric Information and Unemployment

    OpenAIRE

    Robin Boadway; Nicolas Marceau; Maurice Marchand; Marianne Vigneault

    1998-01-01

    We examine how three sources of asymmetric information affect the supply of entrepreneurs and unemployment. In the first case, banks cannot observe entrepreneurs' risk of failure so ration credit. This increases the number of entrepreneurs and the level of unemployment. In the second case, firms cannot observe workers' effort so offer a wage above the market clearing one. This results in unemployment and too few entrepreneurs. The final case arises when firms cannot observe workers' abilities...

  1. Asymmetric Microscopic Driving Behavior Theory

    OpenAIRE

    Yeo, Hwasoo

    2008-01-01

    Numerous theories on traffic have been developed as traffic congestion gains more and more interest in our daily life. To model traffic phenomena, many traffic theorists have adopted theories from other fields such as fluid mechanics and thermodynamics. However, their efforts to model the traffic at a microscopic level have not been successful yet. Therefore, to overcome the limitations of the existing theories we propose a microscopic asymmetric traffic theory based on analysis of individual...

  2. Effciency Concern under Asymmetric Information

    OpenAIRE

    Winschel, Evguenia; Zahn, Philipp

    2012-01-01

    Experimental evidence from simple distribution games supports the view that some individuals have a concern for the effciency of allocations. This motive could be important for the implementation of economic policy proposals. In a typical lab experiment, however, individuals have much more information available than outside the lab. We conduct a lab experiment to test whether asymmetric information influences prosocial behavior in a simple non-strategic interaction. In our setting, a dictator...

  3. High performance of junctionless MOSFET with asymmetric gate

    Science.gov (United States)

    Wang, Ying; Tang, Yan; Sun, Ling-ling; Cao, Fei

    2016-09-01

    In this work, we propose a junctionless MOSFET with asymmetric gates (AG-JL MOSFET). This device is a double gate structure with a lateral offset between the gate, and this leads to different characteristic than a conventional double gate structure. Specifically, the asymmetric gate modulates the effective channel length depending on whether the device is in the ON or OFF state, which this leads to more ideal device characteristics. A comprehensive device performance comparison including the ION/IOFF ratio, subthreshold slope (SS), and drain-induced barrier lowering (DIBL) between the proposed device and a conventional device is presented. The proposed device exhibits superior performance when compared a conventional device, and results show that it is also less sensitive to process variations.

  4. A Convenient Method for Asymmetric Reduction of Acetophenone using Lithium Hydroxide

    OpenAIRE

    NISHIKORI, Hisashi; Mizuno, Tomofumi; 錦織, 寿

    2010-01-01

    Optically active lithium-alkoxide catalyzes asymmetric reduction of ketones and imines with alkoxyhydrosilane as a Lewis base. Lithium salt is generally formed by a mixture of optically active alcohol and n-butyllithium as a metal source, which is too sensitive to moisture to handle in air. However, if n-butyllithium is replaced by another lithium source which is stable in air, a more convenient reaction system results. In this study, we examined the enantioselective reduction of acetophenone...

  5. A molecular simulation study on salt response of polyelectrolyte complexes

    Science.gov (United States)

    Antila, Hanne; van Tassel, Paul; Sammalkorpi, Maria

    2015-03-01

    In aqueous solutions, oppositely charged polymers, polyelectrolytes (PEs) form complexes which are known to be sensitive to added salt with responses ranging from shrinking to full destabilization of the complex. As a specific application of PE complexes, the complex formation of DNA with polycations has been demonstrated to be an effective means of transfecting genetic material in gene therapy. We use all-atom molecular dynamics and coarse-grained Monte Carlo simulations to investigate the effect of excess salt on DNA-polycation complex stability. The detailed all-atom simulations demonstrate the mechanism of polycation and ion species specific salt-driven dissociation involving charge reversal. More generally, other possible mechanisms of salt driven dissociation exist as well. The coarse grained approach, which describes the PE complex as oppositely charged, rigid rods and ions as hard spheres, provides a more complete understanding of PE interactions in salt, and suggests possible mechanisms leading to repulsion between the oppositely charged polyelectrolytes.

  6. Characterization of potassium salts of 12-tungstophosphoric acid

    International Nuclear Information System (INIS)

    Potassium salts of 12-tungstophosphoric acid with varying amounts of cation, KxH3-xPW12O40 (x = 1, 2, 3) have been prepared and their characteristics investigated by thermal analyses, FT-IR and micro-Raman spectroscopy and SEM-EDS analysis. It was found that the number of replaced protons by potassium ions in the 12-tungstophosphoric acid structure has influence on the presence of different protonic species, their dynamic equilibrium and on the conductivity of salts. The results reported in this study have been applied to improve the structural model of insoluble acidic salts. It is shown that an acidic potassium salt presents a mixture of neutral salt and unreacted acid. The nature of this mixture depends on the number of replaced protons-oxonium ions by cations. Preliminary measurements with synthesized compounds as solid electrolytes in fuel cells have been done, too.

  7. SALT Science Conference 2015

    Science.gov (United States)

    Buckley, David; Schroeder, Anja

    The Southern African Large Telescope (SALT) has seen great changes in the last years following the beginning of full time science operations in 2011. The three first generation instruments, namely the SALTICAM imager, the Robert Stobie Spectrograph (RSS) and its multiple modes and finally in 2014, the new High Resolution Spectrograph (HRS), have commissioned it. The SALT community now eagerly anticipate the installation and commissioning of the near-infrared arm of RSS, likely to commence in 2016. The the third "Science with SALT" conference was held at the Stellenbosch Institute of Advanced Study from 1-5 June 2015. The goals of this conference were to: -Present and discuss recent results from SALT observations; -Anticipate scientific programs that will be carried out with new SALT instrumentation such as RSS-NIR; -Provide a scientific environment in which to foster inter-institutional and inter-facility collaborations between scientists at the different SALT partners; -Provide an opportunity for students and postdocs to become more engaged in SALT science and operations; -Encourage the scientific strategic planning that will be necessary to insure an important role for SALT in an era of large astronomical facilities in the southern hemisphere such as MeerKAT, the SKA, LSST, and ALMA; -Consider options for future instrumentation and technical development of SALT; and, -Present, discuss, and engage in the SALT Collateral Benefits program led by SAAO. Conference proceedings editors: David Buckley and Anja Schroeder

  8. Incompressibility of asymmetric nuclear matter

    International Nuclear Information System (INIS)

    Using an isospin- and momentum-dependent modified Gogny (MDI) interaction, the Skyrme-Hartree-Fock (SHF) approach, and a phenomenological modified Skyrme-like (MSL) model, we have studied the incompressibility Ksat(δ) of isospin asymmetric nuclear matter at its saturation density. Our results show that in the expansion of Ksat(δ) in powers of isospin asymmetry δ, i.e., Ksat(δ) = K0 + Ksat,2δ2 + Ksat,4δ4 + O(δ6), the magnitude of the 4th-order Ksat,4 parameter is generally small. The 2nd-order Ksat,2 parameter thus essentially characterizes the isospin dependence of the incompressibility of asymmetric nuclear matter at saturation density. Furthermore, the Ksat,2 can be expressed as Ksat,2 = Ksym – 6L – J0/K0 L in terms of the slope parameter L and the curvature parameter Ksym of the symmetry energy and the third-order derivative parameter J0 of the energy of symmetric nuclear matter at saturation density, and we find the higher order J0 contribution to Ksat,2 generally cannot be neglected. Also, we have found a linear correlation between Ksym and L as well as between J0/K0 and K0. Using these correlations together with the empirical constraints on K0 and L, the nuclear symmetry energy Esym(ρ0) at normal nuclear density, and the nucleon effective mass, we have obtained an estimated value of Ksat,2 = -370 ± 120 MeV for the 2nd-order parameter in the isospin asymmetry expansion of the incompressibility of asymmetric nuclear matter at its saturation density. (author)

  9. Asymmetric Information and Consumer Demand

    OpenAIRE

    Ismagilova G. N.; Danilina E. I.; Gafurov I. R.; Ismagilov R. I.; Safiullin L. N.

    2014-01-01

    In the paper study the peculiarities of the formation the consumer demand for durable goods, the so-called «experience goods» in markets with asymmetric information. In the known literature sources studying of the demand is based on the assumption that at the moment of the purchase of goods and services people know exactly what price they are willing to pay for them and what utility they are going to obtain using those goods and services. Consider the signal model in which the initial price a...

  10. Transient Stability During Asymmetrical Faults

    OpenAIRE

    Couturier, Nicolas

    2015-01-01

    This research project has been conducted at RTE in order to study the transient stability after asymmetrical faults. When three-phase short-circuits occur in a network, almost all the electrical power is lost on the relevant line(s). Among all short-circuit types, it is the most drastic event and the issue has to be solved very quickly. But oddly, it is also the easiest problem to solve mathematically speaking. This comes from the fact that the system stays balanced, and equations can be simp...

  11. Phase equilibria in asymmetric mixtures

    International Nuclear Information System (INIS)

    The simplified version of the Perturbed Hard-Chain Theory (SPHCT) is used to compute the phase equilibria and Henry's constants for mixtures in which the molecules are highly asymmetric both in shape and in the intermolecular potential. These mixtures include binary systems such as CO2/hydrocarbons and hydrocarbons/hydrocarbons, which are of particular interest for the oil industry. For this type of mixtures a single parameter (which is calculated from available experimental data of liquid-vapor equilibrium) is introduced. The approach yields results which compare well with the experimental behavior reported in the literature (Author)

  12. Tripartite fully asymmetric universal quantum cloning

    International Nuclear Information System (INIS)

    Full text: We investigate the universal asymmetric cloning of states in a Hilbert space of arbitrary dimension d. We derive the class of optimal and fully asymmetric universal 1 → 3 cloners, which produce three copies, each having a different fidelity. A simple parametric expression for the maximum achievable cloning fidelity triplets will be provided. As a side-product, we also prove the optimality of the 1 → 2 asymmetric cloning machines that have been proposed in the literature. (author)

  13. Enhanced Asymmetric Bilinear Model for Face Recognition

    OpenAIRE

    Wenjuan Gong; Weishan Zhang; Jordi Gonzàlez; Yan Ren; Zhen Li

    2015-01-01

    Bilinear models have been successfully applied to separate two factors, for example, pose variances and different identities in face recognition problems. Asymmetric model is a type of bilinear model which models a system in the most concise way. But seldom there are works exploring the applications of asymmetric bilinear model on face recognition problem with illumination changes. In this work, we propose enhanced asymmetric model for illumination-robust face recognition. Instead of initiali...

  14. Phase transitions in warm, asymmetric nuclear matter

    International Nuclear Information System (INIS)

    A relativistic mean-field model of nuclear matter with arbitrary proton fraction is studied at finite temperature. An analysis is performed of the liquid-gas phase transition in a system with two conserved charges (baryon number and isospin) using the stability conditions on the free energy, the conservation laws, and Gibbs' criteria for phase equilibrium. For a binary system with two phases, the coexistence surface (binodal) is two dimensional. The Maxwell construction through the phase-separation region is discussed, and it is shown that the stable configuration can be determined uniquely at every density. Moreover, because of the greater dimensionality of the binodal surface, the liquid-gas phase transition is continuous (second order by Ehrenfest's definition), rather than discontinuous (first order), as in familiar one-component systems. Using a mean-field equation of state calibrated to the properties of nuclear matter and finite nuclei, various phase-separation scenarios are considered. The model is then applied to the liquid-gas phase transition that may occur in the warm, dilute matter produced in energetic heavy-ion collisions. In asymmetric matter, instabilities that produce a liquid-gas phase separation arise from fluctuations in the proton concentration (chemical instability), rather than from fluctuations in the baryon density (mechanical instability)

  15. 咸水冰融化与土壤入渗过程不同盐分离子迁移规律研究%Study on Migration of Different Salt Ions in Melting and Infiltration Processes of Saline Water Ice

    Institute of Scientific and Technical Information of China (English)

    潘洁; 肖辉; 王立艳; 程文娟; 陆文龙

    2012-01-01

    Simulation and field experiments were conducted to investigate the migration of different salt ions in melting and infiltration processes of saline water ice. The aim of these experiments is to reveal the mechanism of water quality changes in ice melting and the distribution of different ions in different soil depth. The results showed that the content of all salt ions decreased rapidly during ice melting process. However,different ions leached in different rate. The sequence of different ions leaching ratio from high to low was Cl > Mg2+ > K + > Na+ > SP42- > Ca2+ > HCO3 . The difference of ions leaching rate leaded to changes of ions composition in melted water, which reduced sodium adsorption ratio and increased water pH eventually. After irrigation with freezing saline water,all salt ions of soil(0 ~ 80 cm) were decreased except HCO3 , which increased by 6. 85%. The sequence of ions leaching ratio from high to low was Mg2+ > Cl- > Ca2+ > Na+ > K+ > SO42- > HCO3- . Although the leaching ratios of Cl" and Na+ were not the highest, their proportions reached 62. 01 % and 21. 96% in total leaching salt,respectively. Irrigation with freezing saline water changed the ion composition of soil and resulted in alkaline trend in the surface soil. Therefore,freezing irrigation with saline water should be assorted with some measures to prevent soil alkalization.%通过模拟试验及大田试验研究了咸水冰融化过程及土壤入渗过程不同盐分离子迁移分布规律,以期揭示咸水冰融水水质变化机理及咸水结冰灌溉对土壤盐分分布的影响.试验结果表明,咸水冰融化过程各离子含量均急速下降,但不同离子融出速度不同,各离子融出比例高低次序为Cl- >Mg2 >K+ >Na+ >SO4- >Ca2+ >HCO3-;离子融出速度的不同,导致融水离子组成发生变化,最终使融水钠吸附比下降,pH值上升.咸水结冰灌溉使0~ 80 cm土体中除HCO3-增加6.85%以外,其余各

  16. Research on Influence Laws of Different Salt Content and Ion Content to Boundary Moisture Content of Soil%不同含盐量及离子含量对土的界限含水率的影响规律研究

    Institute of Scientific and Technical Information of China (English)

    努尔比亚·吾斯曼; 何建新; 苏枋

    2012-01-01

    The influence laws of the total salt content and different ion content(sulfate and chlorine salt) in fine-grained soil to the boundary moisture content of the soil are studied here in detail.Through artificially making the soil samples with different salt content and ion content,the boundary moisture content of the soil is determined,and the influence of salt content on the boundary moisture content of the soil is studied by using projection pursuit regression analysis method.It is found by analysis that when adding sodium chloride,the hydraulic limit and plastic limit of the soil are decreased with salt content increasing,and when adding sodium sulfate,the hydraulic limit and plastic limit of the soil are risen with salt content increasing.At the same time,when size changing,there appears expand phenomenon.When adding each half of the sodium chloride and sodium sulfate,the hydraulic limit of the soil is dropped obviously,and the plastic limit of the soil is changed a little with salt content increasing.%土中含盐量影响土的物理力学性能,研究细粒土中总盐含量及不同离子含量(硫酸盐和氯盐)对认识土的界限含水率的影响规律有重要意义。人工配制不同含盐量、不同离子含量的土样,测定土的界限含水率,并运用投影寻踪回归分析方法研究含盐量对土的界限含水率的影响。研究结果表明:加氯化钠时,随着含盐量的增加,土的液、塑限均有下降;加硫酸钠时,随着含盐量的增加,土的液、塑限均有上升,体积发生变化,出现膨胀现象;各加一半时,随着含盐量的增加,土的液限明显下降,塑限变化不大。

  17. Hydrogen migration in methanol studied under asymmetric fs laser irradiation

    Science.gov (United States)

    Kotsina, N.; Kaziannis, S.; Kosmidis, C.

    2014-06-01

    Hydrogen migration processes in deuterated methanol (CH3OD) under the irradiation of ultrashort (30 fs) two color (400/800 nm) laser field have been investigated by means of time-of-flight mass spectrometry. The utilization of an asymmetric ω/2ω laser field contributes to a better understanding of hydrogen migration processes. Based on the comparative study of the asymmetry dependence and the angular distributions of the H2D+, HOD+ and H2OD+ fragment ions, whose formation requires hydrogen migration, it was feasible to distinguish the most probable site of the molecular skeleton where the hydrogen migrates from.

  18. Interaction modes between asymmetrically and oppositely charged rods

    Science.gov (United States)

    Antila, Hanne S.; Van Tassel, Paul R.; Sammalkorpi, Maria

    2016-02-01

    The interaction of oppositely and asymmetrically charged rods in salt—a simple model of (bio)macromolecular assembly—is observed via simulation to exhibit two free energy minima, separated by a repulsive barrier. In contrast to similar minima in the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory, the governing mechanism includes electrostatic attraction at large separation, osmotic repulsion at close range, and depletion attraction near contact. A model accounting for ion condensation and excluded volume is shown to be superior to a mean-field treatment in predicting the effect of charge asymmetry on the free-energy profile.

  19. Aneutronic fusion on the base of asymmetrical centrifugal trap

    Science.gov (United States)

    Volosov, V. I.

    2006-08-01

    A physical design of a device that can be a base for a direct-conversion nuclear electric power station is considered. The project considers the aneutronic reaction P-11B in the asymmetric centrifugal trap. Kinetic energy of nuclear particles (alpha particles) is converted into electrical energy inside this device; no thermal cycle is used. Heating and recuperation of energy of protons and boron ions take place in the plasma space. The presented scheme differs significantly from the conventional thermonuclear fusion. 'Fast' protons, which are the main energy component of plasma, have an almost monoenergetic spectrum. This makes it possible to realize the 'resonance' fusion.

  20. Long-wavelength limit of the static structure factors for mixtures of two simple molten salts with a common ion and generalized Bhatia-Thornton formalism: Molecular dynamics study of molten mixture Ag(Br0.7I0.3)

    International Nuclear Information System (INIS)

    The relation between thermodynamic properties and the long-wavelength limit of the structure factors for mixtures of two simple molten salts with a common ion is derived. While the long-wavelength limit of the partial structure factors for binary ionic systems is directly related to the isothermal compressibility, for ternary ionic systems it is shown that it is also related to the mean square thermal fluctuation in the relative concentration of the non-common ions. This result leads to a generalization of the Bhatia-Thornton formalism. From the local fluctuations in the total number-density, charge-density, and relative concentration, six static structure factors, and the corresponding spatial correlation functions, are defined. By introducing three complementary structure factors, it is possible to describe either these mixtures as a system of cations and anions irrespective of the species of the non-common ions, or solely the binary subsystem of the non-common ions. The generalized structure factors and their long-wavelength limits are illustrated by molecular dynamics simulation results of the molten mixture Ag(Br0.7I0.3). The mixture retains the charge order characteristic of pure molten monovalent salts and the topological order observed in monovalent ionic melts in which the cations are smaller than the anions, while the main trends of the anionic chemical order are those of simple binary alloys. The long-wavelength fluctuations in the local relative concentration are found to be very sensitive to the choice of the short-range interactions between the non-common ions

  1. Effect of subsurface drainage on salt movement and distribution in salt-affected soils

    International Nuclear Information System (INIS)

    This study was carried out to evaluate different subsurface drainage treatments (combinations of depth and spacing) on salt movement and distribution. The soil is clay and the drainage was designed according to the steady-state condition (Hooghoudt's equation). Three spacings and two depths resulted in six drainage treatments. Soil samples represented the initial state of every treatment and after 14 months they (cotton followed by wheat) were analysed. The data show that drain depth has its effective role in salt leaching, while drain spacing has its effect on salt distribution in the soil profile. The leaching rate of each specific ion is also affected by the different drainage treatments. In general, the salt movement and distribution should be taken into consideration when evaluating the design of drainage systems. (author)

  2. Aberrations in asymmetrical electron lenses

    International Nuclear Information System (INIS)

    Starting from well established knowledge in light-optics we explore the question if electron-optical aberration can be improved in asymmetrical electron lenses. We show that spherical as well as chromatic aberration coefficients are reduced in asymmetric electrostatic einzel lenses when the center electrode is moved away from the center position towards the entrance electrode. Relative improvements up to 40% for both the chromatic and the spherical aberration coefficients can be obtained. We use analytical and numerical calculations to confirm this result for exemplary cases of a lens with fixed length and working distance. The agreement of the two calculation methods is very good. We then derive an estimate for the electron-optical aberration coefficients from light-optics. The derived expressions for chromatic and spherical aberrations are somewhat simpler than the ones derived from electron-optics as they involve integrals only over the electrostatic potential, not over the electron paths. The estimated formulas still agree well with the electron optical calculations. Overall, we are tempted to suggest that the enormous knowledge base of light optics can provide considerable guidance for electron-optical applications. -- Highlights: ► Develops the analogy between light and electron optics in aberration calculations. ► Optimized spherical and chromatic aberrations for an electrostatic einzel lens. ► Comparison between analytic and numerical aberration calculations.

  3. Aberrations in asymmetrical electron lenses.

    Science.gov (United States)

    Fitzgerald, J P S; Word, R C; Könenkamp, R

    2012-08-01

    Starting from well established knowledge in light-optics we explore the question if electron-optical aberration can be improved in asymmetrical electron lenses. We show that spherical as well as chromatic aberration coefficients are reduced in asymmetric electrostatic einzel lenses when the center electrode is moved away from the center position towards the entrance electrode. Relative improvements up to 40% for both the chromatic and the spherical aberration coefficients can be obtained. We use analytical and numerical calculations to confirm this result for exemplary cases of a lens with fixed length and working distance. The agreement of the two calculation methods is very good. We then derive an estimate for the electron-optical aberration coefficients from light-optics. The derived expressions for chromatic and spherical aberrations are somewhat simpler than the ones derived from electron-optics as they involve integrals only over the electrostatic potential, not over the electron paths. The estimated formulas still agree well with the electron optical calculations. Overall, we are tempted to suggest that the enormous knowledge base of light optics can provide considerable guidance for electron-optical applications. PMID:22206603

  4. Excitons in asymmetric quantum wells

    Science.gov (United States)

    Grigoryev, P. S.; Kurdyubov, A. S.; Kuznetsova, M. S.; Ignatiev, I. V.; Efimov, Yu. P.; Eliseev, S. A.; Petrov, V. V.; Lovtcius, V. A.; Shapochkin, P. Yu.

    2016-09-01

    Resonance dielectric response of excitons is studied for the high-quality InGaAs/GaAs heterostructures with wide asymmetric quantum wells (QWs). To highlight effects of the QW asymmetry, we have grown and studied several heterostructures with nominally square QWs as well as with triangle-like QWs. Several quantum confined exciton states are experimentally observed as narrow exciton resonances. A standard approach for the phenomenological analysis of the profiles is generalized by introducing different phase shifts for the light waves reflected from the QWs at different exciton resonances. Good agreement of the phenomenological fit to the experimentally observed exciton spectra for high-quality structures allowed us to reliably obtain parameters of the exciton resonances: the exciton transition energies, the radiative broadenings, and the phase shifts. A direct numerical solution of the Schrödinger equation for the heavy-hole excitons in asymmetric QWs is used for microscopic modeling of the exciton resonances. Remarkable agreement with the experiment is achieved when the effect of indium segregation is taken into account. The segregation results in a modification of the potential profile, in particular, in an asymmetry of the nominally square QWs.

  5. ASYMMETRIC SOLAR POLAR FIELD REVERSALS

    International Nuclear Information System (INIS)

    The solar polar fields reverse because magnetic flux from decaying sunspots moves toward the poles, with a preponderance of flux from the trailing spots. If there is a strong asymmetry, in the sense that most activity is in the northern hemisphere, then that excess flux will move toward the north pole and reverse that pole first. If there is more activity in the south later on, then that flux will help to reverse the south pole. In this way, two humps in the solar activity and a corresponding difference in the time of reversals develop (in the ideal case). Such a difference was originally noted in the very first observation of polar field reversal just after the maximum of the strongly asymmetric solar cycle 19, when the southern hemisphere was most active before sunspot maximum and the south pole duly reversed first, followed by the northern hemisphere more than a year later, when that hemisphere became most active. Solar cycles since then have had the opposite asymmetry, with the northern hemisphere being most active before solar maximum. We show that polar field reversals for these cycles have all happened in the north first, as expected. This is especially noteworthy for the present solar cycle 24. We suggest that the association of two or more peaks of solar activity when separated by hemispheres with correspondingly different times of polar field reversals is a general feature of the cycle, and that asymmetric polar field reversals are simply a consequence of the asymmetry of solar activity.

  6. Asymmetric Laguerre-Gaussian beams

    Science.gov (United States)

    Kovalev, A. A.; Kotlyar, V. V.; Porfirev, A. P.

    2016-06-01

    We introduce a family of asymmetric Laguerre-Gaussian (aLG) laser beams. The beams have been derived via a complex-valued shift of conventional LG beams in the Cartesian plane. While propagating in a uniform medium, the first bright ring of the aLG beam becomes less asymmetric and the energy is redistributed toward peripheral diffraction rings. The projection of the orbital angular momentum (OAM) onto the optical axis is calculated. The OAM is shown to grow quadratically with increasing asymmetry parameter of the aLG beam, which equals the ratio of the shift to the waist radius. Conditions for the OAM becoming equal to the topological charge have been derived. For aLG beams with zero radial index, we have deduced an expression to define the intensity maximum coordinates and shown the crescent-shaped intensity pattern to rotate during propagation. Results of the experimental generation and rotation of aLG beams agree well with theoretical predictions.

  7. Active matter on asymmetric substrates

    Science.gov (United States)

    Olson Reichhardt, C. J.; Drocco, J.; Mai, T.; Wan, M. B.; Reichhardt, C.

    2011-10-01

    For collections of particles in a thermal bath interacting with an asymmetric substrate, it is possible for a ratchet effect to occur where the particles undergo a net dc motion in response to an ac forcing. Ratchet effects have been demonstrated in a variety of systems including colloids as well as magnetic vortices in type-II superconductors. Here we examine the case of active matter or self-driven particles interacting with asymmetric substrates. Active matter systems include self-motile colloidal particles undergoing catalysis, swimming bacteria, artificial swimmers, crawling cells, and motor proteins. We show that a ratchet effect can arise in this type of system even in the absence of ac forcing. The directed motion occurs for certain particle-substrate interaction rules and its magnitude depends on the amount of time the particles spend swimming in one direction before turning and swimming in a new direction. For strictly Brownian particles there is no ratchet effect. If the particles reflect off the barriers or scatter from the barriers according to Snell's law there is no ratchet effect; however, if the particles can align with the barriers or move along the barriers, directed motion arises. We also find that under certain motion rules, particles accumulate along the walls of the container in agreement with experiment. We also examine pattern formation for synchronized particle motion. We discuss possible applications of this system for self-assembly, extracting work, and sorting as well as future directions such as considering collective interactions and flocking models.

  8. Salt Weathering on Mars

    Science.gov (United States)

    Jagoutz, E.

    2006-12-01

    Large well rounded boulders and angular rock fragments characterizes the Martian landscape as seen on the recent excellent quality photos. Analyzing the different rock-shapes indicates a time sequence of emplacement, fragmentation and transport of different rocks on Mars, which might give interesting insight into transport and weathering processes. Larger commonly well rounded boulders were emplaced onto gravel plains. After emplacement, these rocks were fragmented and disassembled. Nests of angular rock fragments are marking the locations of preexisting larger rocks. Frequently it is possible to reconstruct larger rounded rocks from smaller angular fragments. In other cases transport after fragmentation obscured the relationship of the fragments. However, a strewn field of fragments is still reminiscent of the preexisting rock. Mechanical salt weathering could be a plausible explanation for the insitu fragmentation of larger rounded blocks into angular fragments. Impact or secondary air fall induced fragmentation produces very different patterns, as observed around impact crates on Earth. Salt weathering of rocks is a common process in terrestrial environments. Salt crystallization in capillaries causes fragmentation of rocks, irrespective of the process of salt transportation and concentration. On Earth significant salt weathering can be observed in different climatic environments: in the transition zone of alluvial aprons and salt playas in desserts and in dry valleys of Antarctica. In terrestrial semi-arid areas the salt is transported by salt solution, which is progressively concentrated by evaporation. In Antarctic dry valleys freeze-thaw cycles causes salt transportation and crystallization resulting in rock fragmentation. This salt induced process can lead to complete destruction of rocks and converts rocks to fine sand. The efficient breakdown of rocks is dominating the landscape in some dry valleys of the Earth but possibly also on Mars. (Malin, 1974

  9. Some Remarks on Asymmetric Syntheses from Recent Studies

    OpenAIRE

    Baba, Naomichi

    1990-01-01

    Some asymmetric syntheses were presented here and discussed briefly including NADH model reactions, phase transfer-catalyzed asymmetric epoxidation, enantiotopic group-selective hydrolysis of a malonic anhydride with alkoxide anion, intramolecular acid-catalyzed lactonizations, catalytic asymmetric Diels-Alder synthesis, asymmetric aldol condensation, chiral homoallyl alcohol synthesis, asymmetric addition of diethylzinc to aldehyde, kinetic resolution of racemic hydroperoxides and binaphthol...

  10. Salt Induced Decay of Masonry and Electrokinetic Repair

    DEFF Research Database (Denmark)

    Ottosen, Lisbeth M.; Rörig-Dalgaard, Inge

    salt ions from brick masonry and also how much the removal rate can be increased by application of the electric field compared to diffusion alone. Some main differences occur between electrokinetic remediation of heavy metal polluted soil and electrokinetic removal of salts from brick masonry. The ions...... conductivity of bricks without increased salt content is very low compared to soils in general. Furthermore in a masonry wall there are boundaries with different chemistry (e.g. pH) that the ions must pass, brick-mortar boundaries. From initial experiments with electrokinetic removal of Ca2+ ions from bricks...... good results have been found. The bricks were spiked with Ca(NO3)2 to the brick before the current was applied and it was found that the Ca content of the brick after electrokinetic treatment was even lower than it was originally before the spiking. A series of different duration was conducted and it...

  11. Low-salt diet

    Science.gov (United States)

    ... harmful to you, a salt substitute is a good way to lower the amount of sodium in your diet. Alternate Names Low-sodium diet; Salt restriction Images Low sodium diet References American Heart Association Nutrition Committee; Lichtenstein AH, Appel LJ, Brands M, Carnethon M, Daniels S, et al. Diet and ...

  12. Hydroxycarboxylic acids and salts

    Energy Technology Data Exchange (ETDEWEB)

    Kiely, Donald E; Hash, Kirk R; Kramer-Presta, Kylie; Smith, Tyler N

    2015-02-24

    Compositions which inhibit corrosion and alter the physical properties of concrete (admixtures) are prepared from salt mixtures of hydroxycarboxylic acids, carboxylic acids, and nitric acid. The salt mixtures are prepared by neutralizing acid product mixtures from the oxidation of polyols using nitric acid and oxygen as the oxidizing agents. Nitric acid is removed from the hydroxycarboxylic acids by evaporation and diffusion dialysis.

  13. Geomechanics of bedded salt

    International Nuclear Information System (INIS)

    Creep data from the literature search is reinterpreted by SGI, resulting in a better understanding of the temperature and stress state dependence of the octahedral creep rate and the octahedral shear strength. The concept of a transition strength between the elastic and the plastic states is in agreement with the data. The elastic and rheological properties of salt are described, and a set of constitutive equations is presented. The dependence of material properties on parameters such as temperature is considered. Findings on the permeability of salt are summarized, and the in-situ behavior of openings in bedded salt is described based on extensive engineering experience. A stress measuring system utilizing a finite element computer code is discussed. Geological factors affecting the stability of salt openings are considered, and the Stress Control Technique for designing stable openings in bedded salt formations is explained

  14. Novel graphite salts of high oxidizing potential

    Energy Technology Data Exchange (ETDEWEB)

    McCarron, E.M. III

    1980-08-01

    The intercalation of graphite by the third-transition-series metal hexafluorides has yielded the graphite salts, C/sub 8//sup +/OsF/sub 6//sup -/, C/sub 8//sup +/IrF/sub 6//sup -/ and C/sub 12//sup 2 +/PtF/sub 6//sup 2 -/. The fluoroplatinate salt represents the highest electron withdrawal from the graphite network yet achieved. Analogues to the Os and Ir salts have been obtained both by fluorination of Group V pentaflouride intercalates, C/sub 8/MF/sub 5/ (M = As, Sb), and by the interaction of the dioxygenyl salts with graphite (8C + O/sub 2/MF/sub 6/ ..-->.. C/sub 8/MF/sub 6/ + O/sub 2/+). Non-intercalating binary fluorides have been observed to intercalate in the presence of a fluorine-rich environment (e.g., 8C + PF/sub 5/ + 1/2 F/sub 2/ ..-->.. C/sub 8/PF/sub 6/). GeF/sub 4/, which also does not spontaneously intercalate graphite, has been observed to interact with graphite in the presence of 2 atmospheres of fluorine overpressure to give the fluoroplatinate salt analogue, C/sub 12//sup 2 +/GeF/sub 6//sup 2 -/. This material is in equilibrium with the pentafluorogermanate at ordinary pressures and temperatures. C/sub 12//sup 2 +/GeF/sub 6//sup 2 -/ ..-->.. C/sub 12//sup +/GeF/sub 5//sup -/ + 1/2 F/sub 2/. C/sub 12/GeF/sub 6/ must have an oxidizing potential close to that of fluorine itself. The graphite fluorometallate salts are both electronic and ionic (F/sup -/) conductors. For the C/sub 8//sup +/MF/sub 6//sup -/ salts, a maximum electronic conductivity an order of magnitude greater than the parent graphite has been observed for stage two. The high oxidizing potential, coupled with the fluoride ion transport capability of the graphite salts, has been exploited in the construction of solid-state galvanic cells. These cells use the graphite fluorometallate salts as electrode materials in combination with a superionic fluoride-ion-conducting solid electrolyte.

  15. Condensation on Slippery Asymmetric Bumps

    CERN Document Server

    Park, Kyoo-Chul; He, Neil; Aizenberg, Joanna

    2015-01-01

    Bumps are omnipresent from human skin to the geological structures on planets, which offer distinct advantages in numerous phenomena including structural color, drag reduction, and extreme wettability. Although the topographical parameters of bumps such as radius of curvature of convex regions significantly influence various phenomena including anti-reflective structures and contact time of impacting droplets, the effect of the detailed bump topography on growth and transport of condensates have not been clearly understood. Inspired by the millimetric bumps of the Namib Desert beetle, here we report the identified role of radius of curvature and width of bumps with homogeneous surface wettability in growth rate, coalescence and transport of water droplets. Further rational design of asymmetric convex topography and synergetic combination with slippery coating simultaneously enable self-transport, leading to unseen five-fold higher growth rate and an order of magnitude faster shedding time of droplets compared...

  16. Asymmetric diffusion of cosmic rays

    CERN Document Server

    Medvedev, Mikhail V

    2015-01-01

    Cosmic ray propagation is diffusive because of pitch angle scattering by waves. We demonstrate that if the high-amplitude magnetohydrodynamic turbulence with $\\tilde B/\\langle B\\rangle \\sim 1$ is present on top of the mean field gradient, the diffusion becomes asymmetric. As an example, we consider the vertical transport of cosmic rays in our Galaxy propagating away from a point-like source. We solve this diffusion problem analytically using a one-dimensional Markov chain analysis. We obtained that the cosmic ray density markedly differs from the standard diffusion prediction and has a sizable effect on their distribution throughout the galaxy. The equation for the continuous limit is also derived, which shows limitations of the convection-diffusion equation.

  17. New asymmetric quantum codes over Fq

    Science.gov (United States)

    Ma, Yuena; Feng, Xiaoyi; Xu, Gen

    2016-07-01

    Two families of new asymmetric quantum codes are constructed in this paper. The first family is the asymmetric quantum codes with length n=qm-1 over Fq, where qge 5 is a prime power. The second one is the asymmetric quantum codes with length n=3m-1. These asymmetric quantum codes are derived from the CSS construction and pairs of nested BCH codes. Moreover, let the defining set T1=T2^{-q}, then the real Z-distance of our asymmetric quantum codes are much larger than δ _max+1, where δ _max is the maximal designed distance of dual-containing narrow-sense BCH code, and the parameters presented here have better than the ones available in the literature.

  18. Lithium Titanate Confined in Carbon Nanopores for Asymmetric Supercapacitors.

    Science.gov (United States)

    Zhao, Enbo; Qin, Chuanli; Jung, Hong-Ryun; Berdichevsky, Gene; Nese, Alper; Marder, Seth; Yushin, Gleb

    2016-04-26

    Porous carbons suffer from low specific capacitance, while intercalation-type active materials suffer from limited rate when used in asymmetric supercapacitors. We demonstrate that nanoconfinement of intercalation-type lithium titanate (Li4Ti5O12) nanoparticles in carbon nanopores yielded nanocomposite materials that offer both high ion storage density and rapid ion transport through open and interconnected pore channels. The use of titanate increased both the gravimetric and volumetric capacity of porous carbons by more than an order of magnitude. High electrical conductivity of carbon and the small size of titanate crystals allowed the composite electrodes to achieve characteristic charge and discharge times comparable to that of the electric double-layer capacitors. The proposed composite synthesis methodology is simple, scalable, and applicable for a broad range of active intercalation materials, while the produced composite powders are compatible with commercial electrode fabrication processes. PMID:26950509

  19. Ion mobility sensor system

    Science.gov (United States)

    Xu, Jun; Watson, David B.; Whitten, William B.

    2013-01-22

    An ion mobility sensor system including an ion mobility spectrometer and a differential mobility spectrometer coupled to the ion mobility spectrometer. The ion mobility spectrometer has a first chamber having first end and a second end extending along a first direction, and a first electrode system that generates a constant electric field parallel to the first direction. The differential mobility spectrometer includes a second chamber having a third end and a fourth end configured such that a fluid may flow in a second direction from the third end to the fourth end, and a second electrode system that generates an asymmetric electric field within an interior of the second chamber. Additionally, the ion mobility spectrometer and the differential mobility spectrometer form an interface region. Also, the first end and the third end are positioned facing one another so that the constant electric field enters the third end and overlaps the fluid flowing in the second direction.

  20. Crushed Salt Constitutive Model

    International Nuclear Information System (INIS)

    The constitutive model used to describe the deformation of crushed salt is presented in this report. Two mechanisms -- dislocation creep and grain boundary diffusional pressure solution -- are combined to form the basis for the constitutive model governing the deformation of crushed salt. The constitutive model is generalized to represent three-dimensional states of stress. Upon complete consolidation, the crushed-salt model reproduces the Multimechanism Deformation (M-D) model typically used for the Waste Isolation Pilot Plant (WIPP) host geological formation salt. New shear consolidation tests are combined with an existing database that includes hydrostatic consolidation and shear consolidation tests conducted on WIPP and southeastern New Mexico salt. Nonlinear least-squares model fitting to the database produced two sets of material parameter values for the model -- one for the shear consolidation tests and one for a combination of the shear and hydrostatic consolidation tests. Using the parameter values determined from the fitted database, the constitutive model is validated against constant strain-rate tests. Shaft seal problems are analyzed to demonstrate model-predicted consolidation of the shaft seal crushed-salt component. Based on the fitting statistics, the ability of the model to predict the test data, and the ability of the model to predict load paths and test data outside of the fitted database, the model appears to capture the creep consolidation behavior of crushed salt reasonably well

  1. Molten salt battery having inorganic paper separator

    Science.gov (United States)

    Walker, Jr., Robert D.

    1977-01-01

    A high temperature secondary battery comprises an anode containing lithium, a cathode containing a chalcogen or chalcogenide, a molten salt electrolyte containing lithium ions, and a separator comprising a porous sheet comprising a homogenous mixture of 2-20 wt.% chrysotile asbestos fibers and the remainder inorganic material non-reactive with the battery components. The non-reactive material is present as fibers, powder, or a fiber-powder mixture.

  2. Determination of heat stable salt anions in alkanolamine desulphurization solution by ion chromatography%离子色谱法测定醇胺脱硫溶液中热稳定盐

    Institute of Scientific and Technical Information of China (English)

    唐飞; 汪玉洁; 罗勤; 唐蒙; 陈赓良

    2012-01-01

    为了控制热稳定盐(HSS)对天然气净化装置造成的危害,建立了一种同时检测醇胺脱硫溶液中的乙酸根离子、甲酸根离子、氯离子、硫酸根离子、草酸根离子、硫代硫酸根离子和硫氰酸根离子的离子色谱方法.该方法利用膜过滤、反相固相萃取和稀释3个步骤对工业样品进行前处理,采用氢氧化钾梯度淋洗和电导检测的方式,实现了7种离子的分离与检测.方法的线性范围为0.01~0.5mmol/L,检出限(以信噪比(S/N)为3计)小于0.1 mg/L,回收率为80.0%~100.3%.在5个不同添加浓度下分别测定了上述7个离子,色谱峰面积的重复性良好(相对标准偏差(RSD,n=10)为0.94%~3.99%.通过3个实验室比对试验,表明该方法再现性良好,色谱峰面积的RSD小于5%.应用该方法成功地检测了8家天然气净化厂、3家石油炼厂和1家煤制油工厂的脱硫溶液样品中的HSS,并连续监测某天然气净化装置15 d.该方法具有良好的可靠性和实用性.%To control the potential risk of natural gas purification plants, an Ion chromato-graphic method has been developed to determine the heat stable salts (HSS) in alkanolamine desulphurization solution. Seven HSS anions, including CH3COO-, HCOO-, Cl-, SO2-4, C2O2-4, S2O2-3, SCN-, were determined in a single injection. Before the chromatographic analysis , these industrial samples were pie treated by three steps, i. e. filtration, solid phase extraction and dilution. Using the gradient elution with KOH solution, all of the seven anions have been separated and determined by a conductivity detector. As the calibration results, the linear range of this method was 0. 01 - 0. 5 mmol/L for the 7 anions. The limit of detection ( LOD, S/ N =3) was 0.1 mg/L for each anion. By spiked standard solutions in the samples, the recoveries were in the range of 80. 0% - 100. 3%. The repeatability of this method was evaluated at five different concentrations. The relative

  3. Gases in molten salts

    CERN Document Server

    Tomkins, RPT

    1991-01-01

    This volume contains tabulated collections and critical evaluations of original data for the solubility of gases in molten salts, gathered from chemical literature through to the end of 1989. Within the volume, material is arranged according to the individual gas. The gases include hydrogen halides, inert gases, oxygen, nitrogen, hydrogen, carbon dioxide, water vapor and halogens. The molten salts consist of single salts, binary mixtures and multicomponent systems. Included also, is a special section on the solubility of gases in molten silicate systems, focussing on slags and fluxes.

  4. Pulse radiolysis study of salt effects on reactions of aromatic radical cations with Cl-

    International Nuclear Information System (INIS)

    The effect of quaternary ammonium salts on the decays of the radical cations of biphenyl, trans-stilbene, anthracene and pyrene generated by pulse radiolysis in chlorohydrocarbons has been investigated. The decays, which are due to neutralization reactions with Cl-, are retarded by the addition of salts having non-nucleophilic PF6-, BF4- and ClO4-, whereas the radical cations are rapidly quenched by salts having I- and BPh4-. The retarding effect of the salts is attributed to the formation of ion pairs between the reacting ions and the counter-ions from the salts. The rate constants for the neutralization reactions in 1,2-dichloroethane have been determined for the free-ion and ion-paired states; the latter state is attained by the addition of Bu4NPF6. The rate constant determined in the absence of the salt for Pysup(radical)+ is one order of magnitude smaller than those for the others. The salt effect is also smallest on the reaction of Pysup(radical)+. The charge delocalisation of the large aromatic radical cation may be responsible for the exceptional results for Pysup(radical)+. The largest salt effect was observed on the reaction of Ph2CH+, a charge-localized carbenium ion investigated for comparison. The solvent effect on the neutralization reactions is also discussed. (author)

  5. Salinity tolerance in plants. Quantitative approach to ion transport starting from halophytes and stepping to genetic and protein engineering for manipulating ion fluxes

    OpenAIRE

    Volkov, Vadim

    2015-01-01

    Ion transport is the fundamental factor determining salinity tolerance in plants. The Review starts from differences in ion transport between salt tolerant halophytes and salt-sensitive plants with an emphasis on transport of potassium and sodium via plasma membranes. The comparison provides introductory information for increasing salinity tolerance. Effects of salt stress on ion transport properties of membranes show huge opportunities for manipulating ion fluxes. Further steps require knowl...

  6. Cooking without salt

    Science.gov (United States)

    ... salt. Herbs and spices on vegetables: Carrots -- Cinnamon, cloves, dill, ginger, marjoram, nutmeg, rosemary, sage Corn -- Cumin, ... chopped ¾ cup green peppers 2 tsp vegetable oil 1 8-oz can tomato sauce* 1 tsp ...

  7. What Are Bath Salts?

    Science.gov (United States)

    ... Blog Team Concert festivals are all about good music, good friends, and big crowds. But for some ... school, North Carolina: Are bath salts becoming more popular? Marsha Lopez Hi, Lauren. Nope! Actually quite the ...

  8. Fission product removal from molten salt using zeolite

    International Nuclear Information System (INIS)

    Spent nuclear fuel (SNF) can be treated in a molten salt electrorefiner for conversion into metal and mineral waste forms for geologic disposal. The fuel is dissolved in molten chloride salt. Non-transuranic fission products in the molten salt are ion-exchanged into zeolite A, which is subsequently mixed with glass and consolidated. Zeolite was found to be effective in removing fission product cations from the molten salt. Breakthrough of cesium and the alkaline earths occurred more rapidly than was observed for the rare earths. The effluent composition as a function of time is presented, as well as results for the distribution of fission products along the length of the column. Effects of temperature and salt flow rate are also discussed

  9. Molecular Mechanism of Rice in Response to Salt Stress

    Institute of Scientific and Technical Information of China (English)

    E Zhi-guo; ZHANG Li-jing; WANG Lei

    2011-01-01

    Rice is moderately sensitive to salinity,and the response to salt stress is a complex process,including the perception and transduction of salt stress signal,the activation of specific transcriptional factors and the expression of downstream stress-responsive genes.The functions of Na+ transporters which are involved in the maintenance and reconstruction of the ion homeostasis,transcriptional regulators and osmotic regulation genes were reviewed.Salt tolerance of plants are enhanced by Na+ vacuolar compartmentation or efflux or high levels of osmoprotectants accumulation in cytoplasm.%Rice is moderately sensitive to salinity,and the response to salt stress is a complex process,including the perception and transduction of salt stress signal,the activation of specific transcriptional factors and the expression of downstream stress-respon

  10. Boric Ester-Type Molten Salt via Dehydrocoupling Reaction

    Directory of Open Access Journals (Sweden)

    Noriyoshi Matsumi

    2014-11-01

    Full Text Available Novel boric ester-type molten salt was prepared using 1-(2-hydroxyethyl-3-methylimidazolium chloride as a key starting material. After an ion exchange reaction of 1-(2-hydroxyethyl-3-methylimidazolium chloride with lithium (bis-(trifluoromethanesulfonyl imide (LiNTf2, the resulting 1-(2-hydroxyethyl-3-methylimidazolium NTf2 was reacted with 9-borabicyclo[3.3.1]nonane (9-BBN to give the desired boric ester-type molten salt in a moderate yield. The structure of the boric ester-type molten salt was supported by 1H-, 13C-, 11B- and 19F-NMR spectra. In the presence of two different kinds of lithium salts, the matrices showed an ionic conductivity in the range of 1.1 × 10−4–1.6 × 10−5 S cm−1 at 51 °C. This was higher than other organoboron molten salts ever reported.

  11. The Significance of Interfacial Water Structure in Soluble Salt Flotation Systems.

    Science.gov (United States)

    Hancer, M.; Celik, M. S.; Miller, J. D.

    2001-03-01

    Flotation of soluble salts with dodecyl amine hydrochloride (DAH) and sodium dodecyl sulfate (SDS) collectors has demonstrated that the interfacial water structure and hydration states of soluble salt surfaces together with the precipitation tendency of the corresponding collector salts are of considerable importance in explaining their flotation behavior. In particular, the high concentration of ions in these soluble salt brines and their hydration appear to modify the bulk and interfacial structure of water as revealed by contact angle measurements and this effect is shown to be an important feature in the flotation chemistry of soluble salt minerals including alkali halide and alkali oxyanion salts. Depending on characteristic chemical features (salt type), the salt can serve either as a structure maker, in which intermolecular hydrogen bonding between water molecules is facilitated, or as a structure breaker, in which intermolecular hydrogen bonding between water molecules is disrupted. For structure making salts the brine completely wets the salt surface and no contact angle can be measured. For structure breaking salts the brine does not completely wet the salt surface and a finite contact angle is measured. In this regard it has been found that soluble salt flotation either with the cationic DAH or anionic SDS collector is possible only if the salt is a structure breaker. Copyright 2001 Academic Press. PMID:11237454

  12. Heavy residues from very mass asymmetric heavy ion reactions

    International Nuclear Information System (INIS)

    The isotopic production cross sections and momenta of all residues with nuclear charge (Z) greater than 39 from the reaction of 26, 40, and 50 MeV/nucleon 129Xe + Be, C, and Al were measured. The isotopic cross sections, the momentum distribution for each isotope, and the cross section as a function of nuclear charge and momentum are presented here. The new cross sections are consistent with previous measurements of the cross sections from similar reaction systems. The shape of the cross section distribution, when considered as a function of Z and velocity, was found to be qualitatively consistent with that expected from an incomplete fusion reaction mechanism. An incomplete fusion model coupled to a statistical decay model is able to reproduce many features of these reactions: the shapes of the elemental cross section distributions, the emission velocity distributions for the intermediate mass fragments, and the Z versus velocity distributions. This model gives a less satisfactory prediction of the momentum distribution for each isotope. A very different model based on the Boltzman-Nordheim-Vlasov equation and which was also coupled to a statistical decay model reproduces many features of these reactions: the shapes of the elemental cross section distributions, the intermediate mass fragment emission velocity distributions, and the Z versus momentum distributions. Both model calculations over-estimate the average mass for each element by two mass units and underestimate the isotopic and isobaric widths of the experimental distributions. It is shown that the predicted average mass for each element can be brought into agreement with the data by small, but systematic, variation of the particle emission barriers used in the statistical model. The predicted isotopic and isobaric widths of the cross section distributions can not be brought into agreement with the experimental data using reasonable parameters for the statistical model

  13. Wetting and evaporation of salt-water nanodroplets: A molecular dynamics investigation.

    Science.gov (United States)

    Zhang, Jun; Borg, Matthew K; Sefiane, Khellil; Reese, Jason M

    2015-11-01

    We employ molecular dynamics simulations to study the wetting and evaporation of salt-water nanodroplets on platinum surfaces. Our results show that the contact angle of the droplets increases with the salt concentration. To verify this, a second simulation system of a thin salt-water film on a platinum surface is used to calculate the various surface tensions. We find that both the solid-liquid and liquid-vapor surface tensions increase with salt concentration and as a result these cause an increase in the contact angle. However, the evaporation rate of salt-water droplets decreases as the salt concentration increases, due to the hydration of salt ions. When the water molecules have all evaporated from the droplet, two forms of salt crystals are deposited, clump and ringlike, depending on the solid-liquid interaction strength and the evaporation rate. To form salt crystals in a ring, it is crucial that there is a pinned stage in the evaporation process, during which salt ions can move from the center to the rim of the droplets. With a stronger solid-liquid interaction strength, a slower evaporation rate, and a higher salt concentration, a complete salt crystal ring can be deposited on the surface. PMID:26651708

  14. Wetting and evaporation of salt-water nanodroplets: A molecular dynamics investigation

    Science.gov (United States)

    Zhang, Jun; Borg, Matthew K.; Sefiane, Khellil; Reese, Jason M.

    2015-11-01

    We employ molecular dynamics simulations to study the wetting and evaporation of salt-water nanodroplets on platinum surfaces. Our results show that the contact angle of the droplets increases with the salt concentration. To verify this, a second simulation system of a thin salt-water film on a platinum surface is used to calculate the various surface tensions. We find that both the solid-liquid and liquid-vapor surface tensions increase with salt concentration and as a result these cause an increase in the contact angle. However, the evaporation rate of salt-water droplets decreases as the salt concentration increases, due to the hydration of salt ions. When the water molecules have all evaporated from the droplet, two forms of salt crystals are deposited, clump and ringlike, depending on the solid-liquid interaction strength and the evaporation rate. To form salt crystals in a ring, it is crucial that there is a pinned stage in the evaporation process, during which salt ions can move from the center to the rim of the droplets. With a stronger solid-liquid interaction strength, a slower evaporation rate, and a higher salt concentration, a complete salt crystal ring can be deposited on the surface.

  15. Regenerating a symmetry in asymmetric dark matter.

    Science.gov (United States)

    Buckley, Matthew R; Profumo, Stefano

    2012-01-01

    Asymmetric dark matter theories generically allow for mass terms that lead to particle-antiparticle mixing. Over the age of the Universe, dark matter can thus oscillate from a purely asymmetric configuration into a symmetric mix of particles and antiparticles, allowing for pair-annihilation processes. Additionally, requiring efficient depletion of the primordial thermal (symmetric) component generically entails large annihilation rates. We show that unless some symmetry completely forbids dark matter particle-antiparticle mixing, asymmetric dark matter is effectively ruled out for a large range of masses, for almost any oscillation time scale shorter than the age of the Universe. PMID:22304253

  16. Modelling asymmetric growth in crowded plant communities

    DEFF Research Database (Denmark)

    Damgaard, Christian

    2010-01-01

    A class of models that may be used to quantify the effect of size-asymmetric competition in crowded plant communities by estimating a community specific degree of size-asymmetric growth for each species in the community is suggested. The model consists of two parts: an individual size......-asymmetric growth part, where growth is assumed to be proportional to a power function of the size of the individual, and a term that reduces the relative growth rate as a decreasing function of the individual plant size and the competitive interactions from other plants in the neighbourhood....

  17. Asymmetric warfare and the will to win

    OpenAIRE

    Quinn, Matthew D.

    2001-01-01

    This thesis explores the will to win in asymmetric war. Asymmetric war, in which one side has an overwhelming advantage over its opponent, will likely be the war of the future for the United States in the post-Cold War uni-polar world. To win an asymmetric war, the individual and then the masses must be motivated to fight and, ultimately, the will to win must be cultivated and sustained for victory. Religion is a highly effective motivat or for both the individual and the masses. This motiva...

  18. Crystal structures and hydrogen bonding in the morpholinium salts of four phenoxyacetic acid analogues

    Directory of Open Access Journals (Sweden)

    Graham Smith

    2015-11-01

    Full Text Available The anhydrous salts morpholinium (tetrahydro-2-H-1,4-oxazin-4-ium phenoxyacetate, C4H10NO+·C8H7O3−, (I, morpholinium (4-fluorophenoxyacetate, C4H10NO+·C8H6 FO3−, (II, and isomeric morpholinium (3,5-dichlorophenoxyacetate (3,5-D, (III, and morpholinium (2,4-dichlorophenoxyacetic acid (2,4-D, C4H10NO+·C8H5Cl2O3−, (IV, have been determined and their hydrogen-bonded structures are described. In the crystals of (I, (III and (IV, one of the the aminium H atoms is involved in a three-centre asymmetric cation–anion N—H...O,O′ R12(4 hydrogen-bonding interaction with the two carboxyl O-atom acceptors of the anion. With the structure of (II, the primary N—H...O interaction is linear. In the structures of (I, (II and (III, the second N—H...Ocarboxyl hydrogen bond generates one-dimensional chain structures extending in all cases along [100]. With (IV, the ion pairs are linked though inversion-related N—H...O hydrogen bonds [graph set R42(8], giving a cyclic heterotetrameric structure.

  19. Molten salt reactor type

    International Nuclear Information System (INIS)

    This document is one of the three parts of a first volume devoted to the compilations of American data on the molten salt reactor concept. Emphasize is put essentially on the fuel salt of the primary circuit inside which fission reactions occur. The reasons why the (LiF-BeF2-ThF4-UF4) salt was chosen for the M.S.B.R. concept are examined; the physical, physicochemical and chemical properties of this salt are discussed with its interactions with the structural materials and its evolution in time. An important part of this volume is devoted to the continuous reprocessing of the active salt, the project designers having deemed advisable to take advantage at best from the availability of a continuous purification, in a thermal breeding. The problem of tritium formation and distribution inside the reactor is also envisaged and the fundamentals of the chemistry of the secondary coolant salt are given. The solutions proposed are: the hydrogen scavenging of the primary circuit, a reduction in metal permeability by an oxyde layer deposition on the side in contact with the vapor, and tritium absorption through an isotope exchange with the hydroxifluoroborate

  20. Salt-free vesicle-phases and their template effect

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Researches on the construction, structure, and formation of vesicles formed from surfactants have attracted great attention from colloid and interface chemists. The vesicles formed from salt-free cationic-anionic surfactant systems are very different from those with excess salts, having many particular properties. In this paper, we introduce the properties of vesicles prepared from salt-free surfactant systems, according to our own results, especially the vesicles formed from surfactants with divalent metal ions as counterions in aqueous solutions and room temperature ionic liquids. Moreover, the primary results on template effect of the metal-ligand vesicles have also been summarized.

  1. Optimization of salt adsorption rate in membrane capacitive deionization.

    Science.gov (United States)

    Zhao, R; Satpradit, O; Rijnaarts, H H M; Biesheuvel, P M; van der Wal, A

    2013-04-01

    Membrane capacitive deionization (MCDI) is a water desalination technique based on applying a cell voltage between two oppositely placed porous electrodes sandwiching a spacer channel that transports the water to be desalinated. In MCDI, ion-exchange membranes are positioned in front of each porous electrode to prevent co-ions from leaving the electrode region during ion adsorption, thereby enhancing the salt adsorption capacity. MCDI can be operated at constant cell voltage (CV), or at a constant electrical current (CC). In this paper, we present both experimental and theoretical results for desalination capacity and rate in MCDI (both in the CV- and the CC-mode) as function of adsorption/desorption time, salt feed concentration, electrical current, and cell voltage. We demonstrate how by varying each parameter individually, it is possible to systematically optimize the parameter settings of a given system to achieve the highest average salt adsorption rate and water recovery. PMID:23395310

  2. Transition at the deliquesce point in single salts

    DEFF Research Database (Denmark)

    Rörig-Dalgaard, Inge

    2014-01-01

    ., 1997] a stepwise change in salt state is explained by the diffusion of hydrated Na+ and Cl- ions as hydration of surface ions weakens ionic bond strength to the point where they become mobile. According to [Peters & Ewing, 1997] is NaCl added thin film water at RH above 40 % and they measured the...... increasing numbers of thin film water till 20 mbar at 25˚C whereas the deliquescence point is at 24 mbar. These results suggest a stepwise change in the state of the salt. During preparation to salt calibration tests (in a Dynamic Vapour Sorption equipment (DVS)) the author noticed that some single salts...... have a very sudden and accurate change in salt state whereas another salt changed inaccurate as was noticed with NaCl (seen in more than 10 salt preparations). In the present work, the inaccurate transition between the solid NaCl to NaCl in solution was investigated with a cooling stage (CS) in an ESEM...

  3. Asymmetric Information and Consumer Demand

    Directory of Open Access Journals (Sweden)

    Ismagilova G. N.

    2014-11-01

    Full Text Available In the paper study the peculiarities of the formation the consumer demand for durable goods, the so-called «experience goods» in markets with asymmetric information. In the known literature sources studying of the demand is based on the assumption that at the moment of the purchase of goods and services people know exactly what price they are willing to pay for them and what utility they are going to obtain using those goods and services. Consider the signal model in which the initial price and advertising expenditures are the signals of the quality influencing the formation of the demand for new goods offered by the company of unknown quality through consumer behavior. The basis of this model is the study of producers by consumers, acquisition of knowledge, information about price and quality, as well as their use in order to determine the market share of high-quality goods and low-quality goods in the asymmetry of information.

  4. Chaos suppression through asymmetric coupling

    Science.gov (United States)

    Bragard, J.; Vidal, G.; Mancini, H.; Mendoza, C.; Boccaletti, S.

    2007-12-01

    We study pairs of identical coupled chaotic oscillators. In particular, we have used Roessler (in the funnel and no funnel regimes), Lorenz, and four-dimensional chaotic Lotka-Volterra models. In all four of these cases, a pair of identical oscillators is asymmetrically coupled. The main result of the numerical simulations is that in all cases, specific values of coupling strength and asymmetry exist that render the two oscillators periodic and synchronized. The values of the coupling strength for which this phenomenon occurs is well below the previously known value for complete synchronization. We have found that this behavior exists for all the chaotic oscillators that we have used in the analysis. We postulate that this behavior is presumably generic to all chaotic oscillators. In order to complete the study, we have tested the robustness of this phenomenon of chaos suppression versus the addition of some Gaussian noise. We found that chaos suppression is robust for the addition of finite noise level. Finally, we propose some extension to this research.

  5. Why Do Nucleosomes Unwrap Asymmetrically?

    Science.gov (United States)

    de Bruin, Lennart; Tompitak, Marco; Eslami-Mossallam, Behrouz; Schiessel, Helmut

    2016-07-01

    Nucleosomes, DNA spools with a protein core, engage about three-quarters of eukaryotic DNA and play a critical role in chromosomal processes, ranging from gene regulation, recombination, and replication to chromosome condensation. For more than a decade, micromanipulation experiments where nucleosomes are put under tension, as well as the theoretical interpretations of these experiments, have deepened our understanding of the stability and dynamics of nucleosomes. Here we give a theoretical explanation for a surprising new experimental finding: nucleosomes wrapped onto the 601 positioning sequence (the sequence used in most laboratories) respond highly asymmetrically to external forces by always unwrapping from the same end. Using a computational nucleosome model, we show that this asymmetry can be explained by differences in the DNA mechanics of two very short stretches on the wrapped DNA portion. Our finding suggests that the physical properties of nucleosomes, here the response to forces, can be tuned locally by the choice of the underlying base-pair sequence. This leads to a new view of nucleosomes: a physically highly varied set of DNA-protein complexes whose properties can be tuned on evolutionary time scales to their specific function in the genomic context. PMID:26991771

  6. Twin Higgs Asymmetric Dark Matter.

    Science.gov (United States)

    García García, Isabel; Lasenby, Robert; March-Russell, John

    2015-09-18

    We study asymmetric dark matter (ADM) in the context of the minimal (fraternal) twin Higgs solution to the little hierarchy problem, with a twin sector with gauged SU(3)^{'}×SU(2)^{'}, a twin Higgs doublet, and only third-generation twin fermions. Naturalness requires the QCD^{'} scale Λ_{QCD}^{'}≃0.5-20  GeV, and that t^{'} is heavy. We focus on the light b^{'} quark regime, m_{b^{'}}≲Λ_{QCD}^{'}, where QCD^{'} is characterized by a single scale Λ_{QCD}^{'} with no light pions. A twin baryon number asymmetry leads to a successful dark matter (DM) candidate: the spin-3/2 twin baryon, Δ^{'}∼b^{'}b^{'}b^{'}, with a dynamically determined mass (∼5Λ_{QCD}^{'}) in the preferred range for the DM-to-baryon ratio Ω_{DM}/Ω_{baryon}≃5. Gauging the U(1)^{'} group leads to twin atoms (Δ^{'}-τ^{'}[over ¯] bound states) that are successful ADM candidates in significant regions of parameter space, sometimes with observable changes to DM halo properties. Direct detection signatures satisfy current bounds, at times modified by dark form factors. PMID:26430985

  7. Twin Higgs Asymmetric Dark Matter

    CERN Document Server

    García, Isabel García; March-Russell, John

    2015-01-01

    We study Asymmetric Dark Matter (ADM) in the context of the minimal (Fraternal) Twin Higgs solution to the little hierarchy problem, with a twin sector with gauged $SU(3)' \\times SU(2)'$, a twin Higgs, and only third generation twin fermions. Naturalness requires the QCD$^\\prime$ scale $\\Lambda'_{\\rm QCD} \\simeq 0.5 - 20 \\ {\\rm GeV}$, and $t'$ to be heavy. We focus on the light $b'$ quark regime, $m_{b'} \\lesssim \\Lambda'_{\\rm QCD}$, where QCD$^\\prime$ is characterised by a single scale $\\Lambda'_{\\rm QCD}$ with no light pions. A twin baryon number asymmetry leads to a successful DM candidate: the spin-3/2 twin baryon, $\\Delta' \\sim b'b'b'$, with a dynamically determined mass ($\\sim 5 \\Lambda'_{\\rm QCD}$) in the preferred range for the DM-to-baryon ratio $\\Omega_{\\rm DM}/\\Omega_{\\rm baryon} \\simeq 5$. Gauging the $U(1)'$ group leads to twin atoms ($\\Delta'$ - $\\bar {\\tau'}$ bound states) that are successful ADM candidates in significant regions of parameter space, sometimes with observable changes to DM halo ...

  8. Asymmetric plasmonic induced ionic noise in metallic nanopores

    Science.gov (United States)

    Li, Yi; Chen, Chang; Willems, Kherim; Lagae, Liesbet; Groeseneken, Guido; Stakenborg, Tim; van Dorpe, Pol

    2016-06-01

    We present distinct asymmetric plasmon-induced noise properties of ionic transport observed through gold coated nanopores. We thoroughly investigated the effects of bias voltage and laser illumination. We show that the potential drop across top-coated silicon nanocavity pores can give rise to a large noise asymmetry (~2-3 orders of magnitude). Varying the bias voltage has an appreciable effect on the noise density spectra, typically in the Lorentzian components. The laser power is found to strongly affect the ionic noise level as well as the voltage threshold for light-induced noise generation. The asymmetric noise phenomenon is attributed to plasmon-induced interfacial reactions which promote light-induced charge fluctuation in the ion flow and allow voltage modulation of photo-induced carriers surmounting over such Schottky junctions. We further compare the ionic noise performances of gold nanocavities containing different material stacks, among which thermal oxide passivation of the silicon successfully mitigates the light-induced noise and is also fully CMOS-compatible. The understanding of the described noise characteristics will help to foster multiple applications using related structures including plasmonic-based sensing or plasmon-induced catalysis such as water splitting or solar energy conversion devices.We present distinct asymmetric plasmon-induced noise properties of ionic transport observed through gold coated nanopores. We thoroughly investigated the effects of bias voltage and laser illumination. We show that the potential drop across top-coated silicon nanocavity pores can give rise to a large noise asymmetry (~2-3 orders of magnitude). Varying the bias voltage has an appreciable effect on the noise density spectra, typically in the Lorentzian components. The laser power is found to strongly affect the ionic noise level as well as the voltage threshold for light-induced noise generation. The asymmetric noise phenomenon is attributed to plasmon

  9. Physical mechanism of Eψ-driven current in asymmetric toroidal system

    International Nuclear Information System (INIS)

    Physical mechanism of the Eψ-driven neoclassical current which exists only in asymmetric toroidal systems is clarified. It found that symmetry-breaking, violating the total angular momentum conservation, changes the direction of flow and heat flux to be damped by the parallel viscosities. The change in the direction depends on the collisionality through the gemetric factor which reflects symmetry-breaking. As a result, in contrast to symmetric toroidal systems, the flow and heat flux due to the radial electric field Eψ can damped according to the collisionality in asymmetric toroidal systems. If dominant species such as electrons and primary ions have different collisionalities, there remains a difference between the flows due to Eψ, hence a parallel current proportional directly to the radial electric field, i,e., the Eψ-driven current, is generated in asymmetric toroidal systems in spit of the charge neutrality condition. (author)

  10. Physical mechanism of Eψ-driven current in asymmetric toroidal systems

    International Nuclear Information System (INIS)

    Physical mechanism of the Eψ-driven neoclassical current which exists only in asymmetric toroidal systems is clarified. It is found that symmetry-breaking, violating the total angular momentum conservation, changes the direction of flow and heat flux to be damped by the parallel viscosities. The change in the direction depends on the collisionality through the geometric factor which reflects symmetry-breaking. As a result, in contrast to symmetric toroidal systems, the flow and heat flux due to the radial electric field Eψ can be damped according to the collisionality in asymmetric toroidal systems. If dominant species such as electrons and primary ions have different collisionalities, there remains a difference between the flow due to Eψ, hence a parallel current proportional directly to the radial electric field, i.e., the Eψ-driven current, is generated in asymmetric toroidal systems in spite of the charge neutrality condition. (author)

  11. Asymmetric dense matter in holographic QCD

    Directory of Open Access Journals (Sweden)

    Shin Ik Jae

    2012-02-01

    Full Text Available We study asymmetric dense matter in holographic QCD.We construct asymmetric dense matter by considering two quark flavor branes with dierent quark masses in a D4/D6/D6 model. To calculate the symmetry energy in nuclear matter, we consider two quarks with equal masses and observe that the symmetry energy increases with the total charge showing the stiff dependence. This behavior is universal in the sense that the result is independent of parameters in the model. We also study strange (or hyperon matter with one light and one intermediate mass quarks. In addition to the vacuum properties of asymmetric matter, we calculate meson masses in asymmetric dense matter and discuss our results in the light of in-medium kaon masses.

  12. Massless sunset diagrams in finite asymmetric volumes

    CERN Document Server

    Niedermayer, Ferenc

    2016-01-01

    In this paper we present methods to compute massless sunset diagrams in finite asymmetric volumes in the framework of dimensional regularization and lattice regularization. We also consider 1-loop sums in both regularizations.

  13. Ion-mediated interactions between net-neutral slabs: Weak and strong disorder effects

    Science.gov (United States)

    Ghodrat, Malihe; Naji, Ali; Komaie-Moghaddam, Haniyeh; Podgornik, Rudolf

    2015-12-01

    We investigate the effective interaction between two randomly charged but otherwise net-neutral, planar dielectric slabs immersed in an asymmetric Coulomb fluid containing a mixture of mobile monovalent and multivalent ions. The presence of charge disorder on the apposed bounding surfaces of the slabs leads to substantial qualitative changes in the way they interact, as compared with the standard picture provided by the van der Waals and image-induced, ion-depletion interactions. While, the latter predict purely attractive interactions between strictly neutral slabs, we show that the combined effects from surface charge disorder, image depletion, Debye (or salt) screening, and also, in particular, their coupling with multivalent ions, give rise to a more diverse behavior for the effective interaction between net-neutral slabs at nano-scale separations. Disorder effects show large variation depending on the properly quantified strength of disorder, leading either to non-monotonic effective interaction with both repulsive and attractive branches when the surface charges are weakly disordered (small disorder variance) or to a dominating attractive interaction that is larger both in its range and magnitude than what is predicted from the van der Waals and image-induced, ion-depletion interactions, when the surfaces are strongly disordered (large disorder variance).

  14. Worst Asymmetrical Short-Circuit Current

    DEFF Research Database (Denmark)

    Arana Aristi, Iván; Holmstrøm, O; Grastrup, L;

    2010-01-01

    In a typical power plant, the production scenario and the short-circuit time were found for the worst asymmetrical short-circuit current. Then, a sensitivity analysis on the missing generator values was realized in order to minimize the uncertainty of the results. Afterward the worst asymmetrical...... short-circuit current was analyzed in order to compare the results with the allowable DC current component based in the IEC. Finally the normal operating condition for the power plant was modeled....

  15. Renewable resource management under asymmetric information

    DEFF Research Database (Denmark)

    Jensen, Frank; Andersen, Peder; Nielsen, Max

    Asymmetric information between fishermen and the regulator is important within fisheries. The regulator may have less information about stock sizes, prices, costs, effort, productivity and catches than fishermen. With asymmetric information, a strong analytical tool is principal-agent analysis. In......-productivity agents receive an information rent. The information rent is equivalent to the total incentive cost. The incentive costs arise as we want to reveal the agent's type....

  16. An asymmetric pericyclic cascade approach to oxindoles

    OpenAIRE

    Richmond, Edward

    2014-01-01

    The research in this thesis describes an asymmetric pericyclic cascade approach to the synthesis of a range of enantioenriched oxindoles using enantiopure oxazolidine derived nitrones and disubstituted ketenes. Chapter 1 aims to place this work in the context of the literature, describing other commonly employed or state-of-the-art asymmetric approaches to oxindoles and related compounds. Examples of where these approaches have been used successfully in the total synthesis of related indol...

  17. Asymmetric Federalism in Russia: Cure or Poison?

    OpenAIRE

    Jorge Martinez-Vazquez

    2003-01-01

    In the early years of its existence, the Russian Federation adopted a system of differential treatment of its regions in order to cope with the great degree of diversity present in them. This paper examines the Russian Federation’s asymmetric federalism by evaluating the system’s role, significance and effects on the Federation’s development. The study incorporates a detailed description of the asymmetric federalism over time along with the benefits and costs incurred by its implementation. I...

  18. Asymmetric Membrane Osmotic Capsules for Terbutaline Sulphate

    OpenAIRE

    Gobade, N. G.; Marina Koland; K H Harish

    2012-01-01

    The aim of the present study was to design an asymmetric membrane capsule, an osmotic pump-based drug delivery system of ethyl cellulose for controlled release of terbutaline sulphate. asymmetric membrane capsules contains pore-forming water soluble additive, sorbitol in different concentrations in the capsule shell membrane, which after coming in contact with water, dissolves, resulting in an in situ formation of a microporous structure. The terbutaline sulphate is a β-adrenoreceptor agonist...

  19. Asymmetric septal hypertrophy and hypothyroidism in children.

    OpenAIRE

    Altman, D I; Murray, J.; Milner, S.; Dansky, R; Levin, S. E.

    1985-01-01

    Any echocardiographic study of two children with hypothyroidism demonstrated the presence of asymmetric septal hypertrophy. One child died aged 11 months, and pronounced thickening of the interventricular septum was confirmed at necropsy. There was also hypertrophy of the left ventricular free wall. Histological examination showed only slight muscle fibre disarray, but there was striking vacuolation and hypertrophy of muscle fibres. In the second case, a child aged five years, the asymmetric ...

  20. Synthesis of Reduced Graphene Oxide-Modified LiMn0.75Fe0.25PO4 Microspheres by Salt-Assisted Spray Drying for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Kim, Myeong-Seong; Kim, Hyun-Kyung; Lee, Suk-Woo; Kim, Dong-Hyun; Ruan, Dianbo; Chung, Kyung Yoon; Lee, Sang Hyun; Roh, Kwang Chul; Kim, Kwang-Bum

    2016-01-01

    Microsized, spherical, three-dimensional (3D) graphene-based composites as electrode materials exhibit improved tap density and electrochemical properties. In this study, we report 3D LiMn0.75Fe0.25PO4/reduced graphene oxide microspheres synthesized by one-step salt-assisted spray drying using a mixed solution containing a precursor salt and graphene oxide and a subsequent heat treatment. During this process, it was found that the type of metal salt used has significant effects on the morphology, phase purity, and electrochemical properties of the synthesized samples. Furthermore, the amount of the chelating agent used also affects the phase purity and electrochemical properties of the samples. The composite exhibited a high tap density (1.1 g cm(-3)) as well as a gravimetric capacity of 161 mA h g(-1) and volumetric capacity of 281 mA h cm(-3) at 0.05 C-rate. It also exhibited excellent rate capability, delivering a discharge capacity of 90 mA h g(-1) at 60 C-rate. Furthermore, the microspheres exhibited high energy efficiency and good cyclability, showing a capacity retention rate of 93% after 1000 cycles at 10 C-rate. PMID:27220812

  1. Synthesis of Reduced Graphene Oxide-Modified LiMn0.75Fe0.25PO4 Microspheres by Salt-Assisted Spray Drying for High-Performance Lithium-Ion Batteries

    Science.gov (United States)

    Kim, Myeong-Seong; Kim, Hyun-Kyung; Lee, Suk-Woo; Kim, Dong-Hyun; Ruan, Dianbo; Chung, Kyung Yoon; Lee, Sang Hyun; Roh, Kwang Chul; Kim, Kwang-Bum

    2016-05-01

    Microsized, spherical, three-dimensional (3D) graphene-based composites as electrode materials exhibit improved tap density and electrochemical properties. In this study, we report 3D LiMn0.75Fe0.25PO4/reduced graphene oxide microspheres synthesized by one-step salt-assisted spray drying using a mixed solution containing a precursor salt and graphene oxide and a subsequent heat treatment. During this process, it was found that the type of metal salt used has significant effects on the morphology, phase purity, and electrochemical properties of the synthesized samples. Furthermore, the amount of the chelating agent used also affects the phase purity and electrochemical properties of the samples. The composite exhibited a high tap density (1.1 g cm‑3) as well as a gravimetric capacity of 161 mA h g‑1 and volumetric capacity of 281 mA h cm‑3 at 0.05 C-rate. It also exhibited excellent rate capability, delivering a discharge capacity of 90 mA h g‑1 at 60 C-rate. Furthermore, the microspheres exhibited high energy efficiency and good cyclability, showing a capacity retention rate of 93% after 1000 cycles at 10 C-rate.

  2. Improving the Sensitivity of Matrix-Assisted Ionization (MAI) Mass Spectrometry Using Ammonium Salts.

    Science.gov (United States)

    Chubatyi, Nicholas D; McEwen, Charles N

    2015-10-01

    In matrix-assisted ionization (MAI), analyte incorporated in a small molecule matrix is introduced into an aperture linking atmospheric pressure with the vacuum of a mass spectrometer. Gas-phase analyte ions are spontaneously produced without use of a laser or high voltage. Here we investigate analyte and background ion abundances upon addition of ammonium salts to various MAI matrix/analyte solutions. Regardless of the ammonium salt or matrix used, chemical background ions are suppressed and/or analyte ion abundance improved for basic small molecules, peptides, and proteins. Background ion abundances increase with increasing inlet temperature, but are suppressed with addition of any of a variety of ammonium salts without much effect on the total ion abundances of the analyte ions. However, at lower inlet temperature using the matrices 2-bromo-2-nitropropane-1,3-diol, 1,2-dicyanobenzene, and 3-nitrobenzonitrile (3-NBN), analyte ion abundance increases and any chemical background decreases upon addition of ammonium salt. The improvement in sensitivity using 3-NBN with ammonium salt allows full acquisition mass spectra consuming as little as 1 fmol of ubiquitin. More complete peptide coverage for 100 fmol of a BSA tryptic digest, and increased sensitivity of drugs spiked in urine and saliva were observed after ammonium salt addition to the 3-NBN matrix. PMID:26122522

  3. Plasma and Energetic Particle Behaviors During Asymmetric Magnetic Reconnection at the Magnetopause

    Science.gov (United States)

    Lee, S. H.; Zhang, H.; Zong, Q.-G.; Otto, A.; Sibeck, D. G.; Wang, Y.; Glassmeier, K.-H.; Daly, P.W.; Reme, H.

    2014-01-01

    The factors controlling asymmetric reconnection and the role of the cold plasma population in the reconnection process are two outstanding questions. We present a case study of multipoint Cluster observations demonstrating that the separatrix and flow boundary angles are greater on the magnetosheath than on the magnetospheric side of the magnetopause, probably due to the stronger density than magnetic field asymmetry at this boundary. The motion of cold plasmaspheric ions entering the reconnection region differs from that of warmer magnetosheath and magnetospheric ions. In contrast to the warmer ions, which are probably accelerated by reconnection in the diffusion region near the subsolar magnetopause, the colder ions are simply entrained by ??×?? drifts at high latitudes on the recently reconnected magnetic field lines. This indicates that plasmaspheric ions can sometimes play only a very limited role in asymmetric reconnection, in contrast to previous simulation studies. Three cold ion populations (probably H+, He+, and O+) appear in the energy spectrum, consistent with ion acceleration to a common velocity.

  4. Construction of thermionic alkali-ion sources

    Energy Technology Data Exchange (ETDEWEB)

    Ul Haq, F.

    1986-04-01

    A simple technique is described by which singly charged alkali ions of K, Na, Li, Rb and Cs are produced by heating ultra-pure chemical salts of different alkali metals on tungsten filaments without employing a temperature measuring device. The character of alkali-ion currents at different heating powers and the remarkably constant ion emission current for prolonged periods are discussed.

  5. Safe in salt

    International Nuclear Information System (INIS)

    The geologic history of the 'Germanic Basin', in which saline sediments were piled up in different strata over a period of nearly 100 million years, and the formation of 'salt deposits' as a consequence of tectonic movements (strata bends, dislocations of strata) in the north-west german region are described. As compact rock being 'harnessed' in the ground, mineral salt is completely impermeable to gases and liquids. Its plasticity prevents any formation of pores or crevasses resp. eliminates existing ones. This impermeable quality has been used technically for a long time in order to use solution-mined caverns for the storage of petroleum or gas without containers. Furthermore, for storing radioactive substances it is of particular importance that mineral salt has the highest thermal conductivity of all sedimentary rocks, so that a local heat up will be distributed quickly. All considerations on a safe storage stem from the fact that all actions take place within rock-mechanically homogeneous mineral salt. Bands of different rocks lead to discontinuities and may render a mechanical calculation impossible in some cases. A careful exploration of the internal structure of salt deposits is therefore one of the most important prerequisites for a safe storage of substances to be separated from the biosphere. (RB)

  6. Fundamental Properties of Salts

    Energy Technology Data Exchange (ETDEWEB)

    Toni Y Gutknecht; Guy L Fredrickson

    2012-11-01

    Thermal properties of molten salt systems are of interest to electrorefining operations, pertaining to both the Fuel Cycle Research & Development Program (FCR&D) and Spent Fuel Treatment Mission, currently being pursued by the Department of Energy (DOE). The phase stability of molten salts in an electrorefiner may be adversely impacted by the build-up of fission products in the electrolyte. Potential situations that need to be avoided, during electrorefining operations, include (i) fissile elements build up in the salt that might approach the criticality limits specified for the vessel, (ii) electrolyte freezing at the operating temperature of the electrorefiner due to changes in the liquidus temperature, and (iii) phase separation (non-homogenous solution). The stability (and homogeneity) of the phases can be monitored by studying the thermal characteristics of the molten salts as a function of impurity concentration. Simulated salt compositions consisting of the selected rare earth and alkaline earth chlorides, with a eutectic mixture of LiCl-KCl as the carrier electrolyte, were studied to determine the melting points (thermal characteristics) using a Differential Scanning Calorimeter (DSC). The experimental data were used to model the liquidus temperature. On the basis of the this data, it became possible to predict a spent fuel treatment processing scenario under which electrorefining could no longer be performed as a result of increasing liquidus temperatures of the electrolyte.

  7. Salt-induced contraction of polyelectrolyte brushes

    International Nuclear Information System (INIS)

    We present an experimental study dedicated to understanding the behaviour of polyelectrolyte chains when salt goes into a polyelectrolyte brush. We use the ability of asymmetric neutral-charged diblock copolymers to anchor to a selective interface or to self-assemble in water, to examine polyelectrolyte brushes both in planar and in spherical geometries. Using neutron reflectivity, the monomer profile of planar brushes has been found to switch from a Gaussian profile to a parabolic profile, showing that at large spatial scale a salted planar brush behaves like a neutral one in good solvent. Using small angle neutron scattering, it is found that spherical brushes exhibit the same behaviour at a large spatial scale although polyelectrolyte chains remain rod-like at a small spatial scale whatever the salinity is. The charged chains inside a polyelectrolyte brush could be viewed as 'surveyor's chains', which fold their rod-like segments of persistence length lp. In the last part, spherical polyelectrolyte brushes in contact have been examined. Their behaviour is discussed in terms of interdigitation or contraction of the brushes

  8. 气相色谱-高场非对称波形离子迁移谱(GC-FAIMS)法应用于白酒的风味研究%Study on liquor flavor by gas chromatography-field asymmetric ion mobility spectrometry method

    Institute of Scientific and Technical Information of China (English)

    李娟; 郭亚洁; 赵伟军; 李灵峰; 李鹏; 汪小知

    2014-01-01

    目的:将 FAIMS 与 GC 分离技术联用,建立白酒中风味物质的甄别分析方法。方法首先利用 GC的高分离能力对白酒成分进行预分离,避免了干扰组分带来的离子竞争等问题;然后用 GC-FAIMS 进行检测;最后通过质谱对 GC-FAIMS 谱图中风味物质的出峰信号进行确认,并以各种风味物质含量为依据,通过主成分分析(PCA)法对白酒的不同香型进行划分。结果枝江大曲负模式下各组分峰的保留时间RSD均小于2.15%,峰高RSD均小于3.06%(n=5),系统的稳定性良好。对11种不同香型的白酒进行GC-FAIMS测试,在负模式下响应的组分主要是有机酸类物质。11种不同香型白酒具有较大的象限差异,能够通过PCA分析方法加以区分。结论 GC-FAIMS 联用技术成功实现了多种白酒的香型分析,该联用技术对复杂体系的分析具有一定的应用前景。%ABSTRACT:Objective To establish a method for identification analysis of flavor in liquors. Methods Liq-uor were separated by gas chromatography (GC) technology to avoid the ion of competition issues caused by the interference components, and determined by GC-high-field asymmetric waveform ion mobility spectrome-try (FAIMS). Finally, the peak signal of flavor compounds was confirmed by the mass spectra. Flavor of liquors were analyzed via PSA method. Results The RSDs of retention time were less than 2.15%, and high peak RSDs were below 3.06%(n=5) of each component in negative mode of Zhijiang Daqu, so the stability of the system was good. Response components of 11 kinds of different flavor liquors detected were the organic acids in negative mode. Different quadrant wine showed a great difference, which could be distinguished by PCA analysis methods. Conclusion GC-FAIMS is successfully implemented in liquor flavor analysis. It has an promising application prospect in dealing with complex sample system.

  9. Electrostatic Interactions of Asymmetrically Charged Membranes

    OpenAIRE

    Ben-Yaakov, Dan; Burak, Yoram; Andelman, David; Safran, S. A.

    2007-01-01

    We predict the nature (attractive or repulsive) and range (exponentially screened or long-range power law) of the electrostatic interactions of oppositely charged and planar plates as a function of the salt concentration and surface charge densities (whose absolute magnitudes are not necessarily equal). An analytical expression for the crossover between attractive and repulsive pressure is obtained as a function of the salt concentration. This condition reduces to the high-salt limit of Parse...

  10. Fatigue in asymmetric-field-driven ferroelectric thin films

    International Nuclear Information System (INIS)

    The polarization fatigue problems in asymmetric-field-driven ferroelectric thin films is investigated in present Letter. The refreshment of fatigue induced by the application of asymmetric voltage to the top and bottom electrodes is modeled by asymmetric Schottky voltage barrier of a quantum well structure. The fatigue behavior under various asymmetric driving voltages and asymmetric driving pulses have been studied. Theoretical calculations are shown to be in agreement with experimental results

  11. Clean Salt integrated flowsheet

    International Nuclear Information System (INIS)

    The Clean Salt Process (CSP) is a novel waste management scheme that removes sodium nitrate and aluminum nitrate nonahydrate as decontaminated (low specific activity) salts from Hanford's high-level waste (HLW). The full scale process will separate the bulk of the waste that exists as sodium salts from the small portion of the waste that is by definition radioactive and dangerous. This report presents initial conceptual CSP flowsheets and demonstrates the benefit of integrating the process into the Tank Waste Remediation Systems (TWRS) Reference Flowsheet. Total HLW and low-level (LLW) volumes are reported for two different CSP integration options and are compared to the TWRS Reference Flowsheet values. The results for a single glass option eliminating LLW disposal are also reported

  12. Gas releases from salt

    Energy Technology Data Exchange (ETDEWEB)

    Ehgartner, B.; Neal, J.; Hinkebein, T.

    1998-06-01

    The occurrence of gas in salt mines and caverns has presented some serious problems to facility operators. Salt mines have long experienced sudden, usually unexpected expulsions of gas and salt from a production face, commonly known as outbursts. Outbursts can release over one million cubic feet of methane and fractured salt, and are responsible for the lives of numerous miners and explosions. Equipment, production time, and even entire mines have been lost due to outbursts. An outburst creates a cornucopian shaped hole that can reach heights of several hundred feet. The potential occurrence of outbursts must be factored into mine design and mining methods. In caverns, the occurrence of outbursts and steady infiltration of gas into stored product can effect the quality of the product, particularly over the long-term, and in some cases renders the product unusable as is or difficult to transport. Gas has also been known to collect in the roof traps of caverns resulting in safety and operational concerns. The intent of this paper is to summarize the existing knowledge on gas releases from salt. The compiled information can provide a better understanding of the phenomena and gain insight into the causative mechanisms that, once established, can help mitigate the variety of problems associated with gas releases from salt. Outbursts, as documented in mines, are discussed first. This is followed by a discussion of the relatively slow gas infiltration into stored crude oil, as observed and modeled in the caverns of the US Strategic Petroleum Reserve. A model that predicts outburst pressure kicks in caverns is also discussed.

  13. Mechanism for salt scaling

    Science.gov (United States)

    Valenza, John J., II

    Salt scaling is superficial damage caused by freezing a saline solution on the surface of a cementitious body. The damage consists of the removal of small chips or flakes of binder. The discovery of this phenomenon in the early 1950's prompted hundreds of experimental studies, which clearly elucidated the characteristics of this damage. In particular it was shown that a pessimum salt concentration exists, where a moderate salt concentration (˜3%) results in the most damage. Despite the numerous studies, the mechanism responsible for salt scaling has not been identified. In this work it is shown that salt scaling is a result of the large thermal expansion mismatch between ice and the cementitious body, and that the mechanism responsible for damage is analogous to glue-spalling. When ice forms on a cementitious body a bi-material composite is formed. The thermal expansion coefficient of the ice is ˜5 times that of the underlying body, so when the temperature of the composite is lowered below the melting point, the ice goes into tension. Once this stress exceeds the strength of the ice, cracks initiate in the ice and propagate into the surface of the cementitious body, removing a flake of material. The glue-spall mechanism accounts for all of the characteristics of salt scaling. In particular, a theoretical analysis is presented which shows that the pessimum concentration is a consequence of the effect of brine pockets on the mechanical properties of ice, and that the damage morphology is accounted for by fracture mechanics. Finally, empirical evidence is presented that proves that the glue-small mechanism is the primary cause of salt scaling. The primary experimental tool used in this study is a novel warping experiment, where a pool of liquid is formed on top of a thin (˜3 mm) plate of cement paste. Stresses in the plate, including thermal expansion mismatch, result in warping of the plate, which is easily detected. This technique revealed the existence of

  14. Asymmetric electrochemical supercapacitor, based on polypyrrole coated carbon nanotube electrodes

    International Nuclear Information System (INIS)

    Highlights: • Polypyrrole (PPy) coated multiwalled carbon nanotubes (MWCNT) were prepared. • New method is based on the use of new electrochemically active dopants for PPy. • The dopans provided dispersion of MWCNT and promoted PPy coating formation. • Symmetric PPy–MWCNT supercapacitors showed high capacitance and low resistance. • Asymmetric PPy–MWCNT/VN–MWCNT devices and modules allowed larger voltage window. - Abstract: Conductive polypyrrole (PPy) polymer – multiwalled carbon nanotubes (MWCNT) composites were synthesized using sulfanilic acid azochromotrop (SPADNS) and sulfonazo III sodium salt (CHR-BS) as anionic dopants for chemical polymerization of PPy. The composites were tested for application in electrodes of electrochemical supercapacitors (ES). Sedimentation tests, electrophoretic deposition experiments and Fourier transform infrared spectroscopy (FTIR) investigations showed that strong adsorption of anionic CHR-BS on MWCNT provided MWCNT dispersion. The analysis of scanning and transmission electron microscopy data demonstrated that the use of CHR-BS allowed the formation of PPy coatings on MWCNT. As a result, the composites, prepared using CHR-BS, showed higher capacitance, compared to the composites, prepared using SPADNS. The electrodes, containing MWCNT, coated with PPy showed a capacitance of 179 F g−1 for active mass loading of 10 mg cm−2, good capacitance retention at scan rates in the range of 2–100 mV s−1 and excellent cyclic stability. Asymmetric ES devices, containing positive PPy–MWCNT electrodes and negative vanadium nitride (VN)–MWCNT electrodes showed significant improvement in energy storage performance, compared to the symmetric ES due to the larger voltage window. The low impedance and high capacitance of the individual cells paved the way to the development of modules with higher voltage, which showed good electrochemical performance

  15. Asymmetric plasmonic induced ionic noise in metallic nanopores.

    Science.gov (United States)

    Li, Yi; Chen, Chang; Willems, Kherim; Lagae, Liesbet; Groeseneken, Guido; Stakenborg, Tim; Van Dorpe, Pol

    2016-06-16

    We present distinct asymmetric plasmon-induced noise properties of ionic transport observed through gold coated nanopores. We thoroughly investigated the effects of bias voltage and laser illumination. We show that the potential drop across top-coated silicon nanocavity pores can give rise to a large noise asymmetry (∼2-3 orders of magnitude). Varying the bias voltage has an appreciable effect on the noise density spectra, typically in the Lorentzian components. The laser power is found to strongly affect the ionic noise level as well as the voltage threshold for light-induced noise generation. The asymmetric noise phenomenon is attributed to plasmon-induced interfacial reactions which promote light-induced charge fluctuation in the ion flow and allow voltage modulation of photo-induced carriers surmounting over such Schottky junctions. We further compare the ionic noise performances of gold nanocavities containing different material stacks, among which thermal oxide passivation of the silicon successfully mitigates the light-induced noise and is also fully CMOS-compatible. The understanding of the described noise characteristics will help to foster multiple applications using related structures including plasmonic-based sensing or plasmon-induced catalysis such as water splitting or solar energy conversion devices. PMID:27273622

  16. Orientation of x-lines in asymmetric magnetic reconnection

    Science.gov (United States)

    Liu, Yi-Hsin; Hesse, Michael; Kuznetsova, Masha

    2015-11-01

    At Earth's magnetopause, reconnection proceeds asymmetrically between magnetosheath plasmas, namely solar wind plasmas compressed by Earth's bow shock, and magnetospheric plasmas. In an asymmetric configuration, it is unclear if there is a simple principle to determine the orientation of the x-line. Using fully kinetic simulations, we study this issue and a spatially localized perturbation is employed to induce a single x-line, that has sufficient freedom to choose its orientation in three-dimensional systems. The effect of ion to electron mass ratio is investigated, and the x-line appears to bisect the magnetic shear angle across the current sheet in the large mass ratio limit. The deviation from the bisection angle in the lower mass ratio limit can be explained by the physics of tearing instability. The local physics control of the x-line orientation studied in this slab geometry could potentially interplay with global geometrical effects to determine the location of collisionless magnetic reconnection at Earth's magnetopause.

  17. Asymmetric switching in a homodimeric ABC transporter: a simulation study.

    Directory of Open Access Journals (Sweden)

    Jussi Aittoniemi

    2010-04-01

    Full Text Available ABC transporters are a large family of membrane proteins involved in a variety of cellular processes, including multidrug and tumor resistance and ion channel regulation. Advances in the structural and functional understanding of ABC transporters have revealed that hydrolysis at the two canonical nucleotide-binding sites (NBSs is co-operative and non-simultaneous. A conserved core architecture of bacterial and eukaryotic ABC exporters has been established, as exemplified by the crystal structure of the homodimeric multidrug exporter Sav1866. Currently, it is unclear how sequential ATP hydrolysis arises in a symmetric homodimeric transporter, since it implies at least transient asymmetry at the NBSs. We show by molecular dynamics simulation that the initially symmetric structure of Sav1866 readily undergoes asymmetric transitions at its NBSs in a pre-hydrolytic nucleotide configuration. MgATP-binding residues and a network of charged residues at the dimer interface are shown to form a sequence of putative molecular switches that allow ATP hydrolysis only at one NBS. We extend our findings to eukaryotic ABC exporters which often consist of two non-identical half-transporters, frequently with degeneracy substitutions at one of their two NBSs. Interestingly, many residues involved in asymmetric conformational switching in Sav1866 are substituted in degenerate eukaryotic NBS. This finding strengthens recent suggestions that the interplay of a consensus and a degenerate NBS in eukaroytic ABC proteins pre-determines the sequence of hydrolysis at the two NBSs.

  18. Bifunctional phase-transfer catalysis in the asymmetric synthesis of biologically active isoindolinones

    Science.gov (United States)

    Di Mola, Antonia; Tiffner, Maximilian; Scorzelli, Francesco; Palombi, Laura; Filosa, Rosanna; De Caprariis, Paolo

    2015-01-01

    Summary New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key building block for a variety of biologically relevant isoindolinones. With this chiral compound in hand, the development of further transformations allowed for the synthesis of diverse derivatives of high pharmaceutical value, such as the Belliotti (S)-PD172938 and arylated analogues with hypnotic sedative activity, obtained in good overall total yield (50%) and high enantiomeric purity (95% ee). The synthetic routes developed herein are particularly convenient in comparison with the current methods available in literature and are particularly promising for large scale applications. PMID:26734105

  19. Linear regression analysis of potentiometric titration data for asymmetric redox reactions

    International Nuclear Information System (INIS)

    A statistical method of processing the curves of potentiometric titration for homogeneous asymmetric redox reactions has been suggested. The method was tested using a model titrimetric system Mohr's salt-K2Cr2O7 and was employed for Te determination in an individual solution, semiconductor alloy and CdTe ceramics. Random error of the equivalence point evaluation by the data of a specific titration of 0.1-0.01 M solutions does not exceed 0.3% in case of titration of 0.001 M solutions it increases up to 1.2%. The value of sr varies from 0.0006 to 0.007

  20. Bifunctional phase-transfer catalysis in the asymmetric synthesis of biologically active isoindolinones.

    Science.gov (United States)

    Di Mola, Antonia; Tiffner, Maximilian; Scorzelli, Francesco; Palombi, Laura; Filosa, Rosanna; De Caprariis, Paolo; Waser, Mario; Massa, Antonio

    2015-01-01

    New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key building block for a variety of biologically relevant isoindolinones. With this chiral compound in hand, the development of further transformations allowed for the synthesis of diverse derivatives of high pharmaceutical value, such as the Belliotti (S)-PD172938 and arylated analogues with hypnotic sedative activity, obtained in good overall total yield (50%) and high enantiomeric purity (95% ee). The synthetic routes developed herein are particularly convenient in comparison with the current methods available in literature and are particularly promising for large scale applications. PMID:26734105

  1. Control of apoptosis by asymmetric cell division.

    Science.gov (United States)

    Hatzold, Julia; Conradt, Barbara

    2008-04-01

    Asymmetric cell division and apoptosis (programmed cell death) are two fundamental processes that are important for the development and function of multicellular organisms. We have found that the processes of asymmetric cell division and apoptosis can be functionally linked. Specifically, we show that asymmetric cell division in the nematode Caenorhabditis elegans is mediated by a pathway involving three genes, dnj-11 MIDA1, ces-2 HLF, and ces-1 Snail, that directly control the enzymatic machinery responsible for apoptosis. Interestingly, the MIDA1-like protein GlsA of the alga Volvox carteri, as well as the Snail-related proteins Snail, Escargot, and Worniu of Drosophila melanogaster, have previously been implicated in asymmetric cell division. Therefore, C. elegans dnj-11 MIDA1, ces-2 HLF, and ces-1 Snail may be components of a pathway involved in asymmetric cell division that is conserved throughout the plant and animal kingdoms. Furthermore, based on our results, we propose that this pathway directly controls the apoptotic fate in C. elegans, and possibly other animals as well. PMID:18399720

  2. Asymmetric bilayer graphene nanoribbon MOSFETs for analog and digital electronics

    Science.gov (United States)

    Dinarvand, A.; Ahmadi, V.; Darvish, Gh.

    2016-05-01

    In this paper, a new structure was proposed for bilayer graphene nanoribbon field-effect transistor (BGNFET) mainly to enhance the electrical characteristics in analog and digital applications. The proposed device uses two metallic gates on the top and bottom of a bilayer graphene nanoribbon, which is surrounded by SiO2 and connected to heavily doped source/drain contacts. Electrical properties of the proposed device were explored using fully self-consistent solution of Poisson and Schrödinger equations based on the nonequilibrium Green's function (NEGF) formalism. Significant improvements in the electrical behavior was seen in the simulation results for gates asymmetrically biased. The comparison with graphene nanoribbon FET showed that the proposed structure benefited from higher intrinsic voltage gain and cut-off frequency and improved switching characteristics such as delay and Ion/Ioff ratio.

  3. Performance-Enhancing Asymmetric Separator for Lithium-Sulfur Batteries.

    Science.gov (United States)

    Conder, Joanna; Forner-Cuenca, Antoni; Gubler, Elisabeth Müller; Gubler, Lorenz; Novák, Petr; Trabesinger, Sigita

    2016-07-27

    Asymmetric separators with polysulfide barrier properties consisting of porous polypropylene grafted with styrenesulfonate (PP-g-PLiSS) were characterized in lithium-sulfur cells to assess their practical applicability. Galvanostatic cycling at different C-rates with and without an electrolyte additive and cyclic voltammetry were used to probe the electrochemical performance of the cells with the PP-g-PLiSS separators and to compare it with the performance of the cells utilizing state-of-the-art separator, Celgard 2400. Overall, it was found that regardless of the applied cycling rate, the use of the grafted separators greatly enhances the Coulombic efficiency of the cell. An appropriate Li-exchange-site (-SO3(-)) concentration at and near the surface of the separator was found to be essential to effectively suppress the polysulfide shuttle without sacrificing the Li-ion mobility through the separator and to improve the practical specific charge of the cell. PMID:27367443

  4. Learning SaltStack

    CERN Document Server

    Myers, Colton

    2015-01-01

    If you are a system administrator who manages multiple servers, then you know how difficult it is to keep your infrastructure in line. If you've been searching for an easier way, this book is for you. No prior experience with SaltStack is required.

  5. Salt repository design approach

    International Nuclear Information System (INIS)

    This paper presents a summary discussion of the approaches that have been and will be taken in design of repository facilities for use with disposal of radioactive wastes in salt formations. Since specific sites have yet to be identified, the discussion is at a general level, supplemented with illustrative examples where appropriate. 5 references, 1 figure

  6. A single pump cycling-column-switching technique coupled with homemade high exchange capacity columns for the determination of iodate in iodized edible salt by ion chromatography with UV detection.

    Science.gov (United States)

    Huang, Zhongping; Subhani, Qamar; Zhu, Zuoyi; Guo, Weiqiang; Zhu, Yan

    2013-08-15

    A single pump cycling-column-switching technique has been developed for the iodate analysis in edible salt. Homemade high exchange capacity columns were adopted for the separation of iodate and chloride. Iodate could be retained and concentrated in a homemade concentrator column after eluents passing through the suppressor. With UV detection, iodate exhibited satisfactory linearity in the range of 0.1-10.0 mg/L with a correlation coefficient of 0.9996. The detection limit (LOD) was 45.53 μg/L, based on the signal-to-noise ratio of 3 (S/N=3) and a 100 μL injection volume. Relative standard deviations (RSDs) for retention time, peak area and peak height were all less than 2.1%. Recoveries of added iodate were in the range of 98.4-101.6% for the spiked samples. The quantitative determination of iodate in edible salt was accomplished by this column-switching technique, without any pretreatment and interference. The results on six samples were statistically compared with results determined by conventional titrimetric method. PMID:23561090

  7. Salt stabilizer for preventing chlorine depletion and increasing shelf-life of potable water - A concept

    Science.gov (United States)

    Copeland, E. J.; Edgerley, R. H.

    1971-01-01

    Proposed concept, based on law of mass action uses addition of salt to increase chlorine ions produced in sodium hydrochlorite solutions, thereby increasing solution shelf-life. This technique is not costly. Usefulness will be determined by acceptability of salt in product undergoing long shelf-life.

  8. HIGH YIELD AND RAPID SYNTHESES METHODS FOR PRODUCING METALLO-ORGANIC SALTS

    DEFF Research Database (Denmark)

    2005-01-01

    A new method for preparing salts of metal cations and organic acids, especially divalent salts of alkaline earth metal ions from group II of the periodic system and carboxylic acids. The method comprising the use of a high temperature (about 90° or more) and, optionally. high pressure, in order to...

  9. Influence of Salts on the Partitioning of 5-Hydroxymethylfurfural in Water/MIBK.

    Science.gov (United States)

    Mohammad, Sultan; Held, Christoph; Altuntepe, Emrah; Köse, Tülay; Sadowski, Gabriele

    2016-04-28

    This study investigates the influence of electrolytes on the performance of extracting 5-hydroxymethylfurfural (HMF) from aqueous media using methyl isobutyl ketone (MIBK). For that purpose, liquid-liquid phase equilibria (LLE) of quaternary systems containing HMF, water, MIBK and salts were measured at atmospheric pressure and 298.15 K. The salts under investigation were composed of one of the anions NO(3-), SO4(2-), Cl(-), or CH3COO(-) and of one of the alkali cations Li(+), Na(+), or K(+). On the basis of these LLE data, the partition coefficient of HMF between the aqueous and the MIBK phase KHMF was determined. It could be shown that KHMF significantly depends on the kind and concentration of the added salt. Weak electrolytes (e.g., sulfates, acetates) caused salting-out, whereas nitrates caused salting-in of HMF to the aqueous phase. Unexpectedly, LiCl caused salting-out at low LiCl concentrations and salting-in at LiCl concentrations higher than 3 mol/kgH2O. The model electrolyte perturbed-chain SAFT (ePC-SAFT) was used to predict the salt influence on the LLE in the quaternary systems water/MIBK/HMF/salt in good agreement with the experimental data. On the basis of ePC-SAFT, it could be concluded that the different salting-out/salting-in behavior of the various salts is mainly caused by their different tendency to form ion pairs in aqueous solutions. PMID:27027570

  10. Composition for preventing salt depositing

    Energy Technology Data Exchange (ETDEWEB)

    Mikhaylov, S.A.; Balakin, V.M.; Lezhenin, V.V.; Litvinets, Yu.I.; Marinin, N.S.; Talankin, V.S.; Yaryshev, G.M.

    1982-01-01

    A composition is proposed for preventing salt depositing which includes polyethylene-polyamine-N-methyl phosphonic acid or its salt and water. It is distinguished by the fact that in order to improve the degree of prevention of the salt depositing under low temperature conditions, it additionally contains ethylene glycol with the following ratio of components (% by mass): polyethylene polyamine-N-methylphosphonic acid or its salt 5-12; ethylene glycol 30-50; water--the rest.

  11. Surviving in a semi-marine habitat: Dietary salt exposure and salt secretion of a New Zealand intertidal skink.

    Science.gov (United States)

    Janssen, Jordi; Towns, David R; Duxbury, Mark; Heitkönig, Ignas M A

    2015-11-01

    Species that inhabit marine and intertidal ecosystems face osmoregulatory challenges, risking dehydration and increased ion concentrations in the body. Lizards need to either tolerate or regulate these increased ion concentrations. In this study, we aim to understand how Suter's skink (Oligosoma suteri), an intertidal skink restricted to shoreline habitats, is able to cope with the physiological stress of living in an extreme salt environment. We determined the diet, prey species' salt content, and nasal and cloacal salt excretion on Rangitoto and Motutapu Islands in northern New Zealand, where the skinks have contrasting access to terrestrial invertebrates. Analysis of stable isotopes suggests inter- and intra-population variability in Suter's skink diets. Intertidal invertebrates under washed up seaweed appear to compose a major part of the diet of the Rangitoto population, while the Motutapu population showed evidence for a mixed diet of terrestrial and intertidal invertebrates. Sodium content of prey species decreased with an increasing distance from the seawater. Field secretion of cations through nasal glands consisted primarily of Na(+), which is consistent with other marine and intertidal species. Sodium was also the primary cation in urine. In contrast, fecal cations consisted primarily of K(+). This first study into the salt secretion of an intertidal skink species provides evidence of Suter's skink's plasticity in secreting excess ions through nasal salt glands. This likely enables it to deal with the challenges of living in a semi-marine habitat. PMID:26188169

  12. Single-step synthesis of no carrier added [18F]fluoroanisols via aryl-heteroaryl-iodonium salts

    International Nuclear Information System (INIS)

    In this study, the high regioselectivity of the nucleophile attack on asymmetric iodonium salts containing the 2-thienyl group was used for preparing [18F]fluoroanisoles as model compounds. The precursor ortho-, meta- and para-methoxyphenyl-2-thienyl-iodonium salts were synthesized as their bromides and iodides according to literature. These iodonium salts were treated with n.c.a. [18]fluoride under various conditions and the desired [18F]fluoroanisoles were obtained in moderate radiochemical yields (RCY=18-42%). (orig.)

  13. Asymmetric Magnon Excitation by Spontaneous Toroidal Ordering

    Science.gov (United States)

    Hayami, Satoru; Kusunose, Hiroaki; Motome, Yukitoshi

    2016-05-01

    The effects of spontaneous toroidal ordering on magnetic excitation are theoretically investigated for a localized spin model that includes a staggered Dzyaloshinsky-Moriya interaction and anisotropic exchange interactions, which arise from the antisymmetric spin-orbit coupling and the multiorbital correlation effect. We show that the model exhibits a Néel-type antiferromagnetic order, which simultaneously accompanies a ferroic toroidal order. We find that the occurrence of toroidal order modulates the magnon dispersion in an asymmetric way with respect to the wave number: a toroidal dipole order on the zigzag chain leads to a band-bottom shift, while a toroidal octupole order on the honeycomb lattice gives rise to a valley splitting. These asymmetric magnon excitations could be a source of unusual magnetic responses, such as nonreciprocal magnon transport. A variety of modulations are discussed while changing the lattice and magnetic symmetries. The implications regarding candidate materials for asymmetric magnon excitations are presented.

  14. Dc SQUIDs with asymmetric shunt resistors

    International Nuclear Information System (INIS)

    We have investigated asymmetrically shunted Nb/Al-AlOx/Nb dc SQUIDs. Simulations based on the coupled Langevin equations predict that the optimum energy resolution ε, and thus also the noise performance of such an asymmetric SQUID, can be 3-4 times better than that of its symmetric counterpart. While keeping the total resistance R identical to a comparable symmetric SQUID with R-1 = R1-1 + R2-1, we shunted only one of the two Josephson junctions with R = R1,2/2. Both types of SQUIDs were characterized with respect to their transport and noise properties at temperature T = 4.2 K, and we compared the experimental results with numerical simulations. Experiments yielded ε ∼ 32 ℎ for an asymmetric SQUID with an inductance L = 22 pH, whereas a comparable symmetric device achieved ε = 110 ℎ.

  15. DNA SECURITY USING SYMMETRIC AND ASYMMETRIC CRYPTOGRAPHY

    Directory of Open Access Journals (Sweden)

    Radu Terec

    2011-01-01

    Full Text Available This paper presents alternative security methods based on DNA. From the available alternative security methods, symmetric DNA algorithms were developed and implemented. The first symmetric DNA algorithm was implemented in the Java language, while the second DNA algorithm was implemented in BioJava and MatLab. Comparisons have been made between the performances of different standard symmetrical algorithms and the DNA proposed algorithms. As a new step to enhance the security, an asymmetric key generation inside a DNA security algorithm is presented. The asymmetric key generation algorithm starts from a password phrase. The asymmetric DNA algorithm proposes a mechanism which makes use of more encryption technologies. Therefore, it is more reliable and more powerful than the OTP DNA symmetric algorithms.

  16. Asymmetric Composite Nanoparticles with Anisotropic Surface Functionalities

    Directory of Open Access Journals (Sweden)

    Donglu Shi

    2009-01-01

    Full Text Available Asymmetric inorganic/organic composite nanoparticles with anisotropic surface functionalities represent a new approach for creating smart materials, requiring the selective introduction of chemical groups to dual components of composite, respectively. Here, we report the synthesis of snowman-like asymmetric silica/polystyrene heterostructure with anisotropic functionalities via a chemical method, creating nanostructure possibly offering two-sided biologic accessibility through the chemical groups. Carboxyl group was introduced to polystyrene component of the snowman-like composites by miniemulsion polymerization of monomer on local surface of silica particles. Moreover, amino group was then grafted to remained silica surface through facile surface modification of the composite nanoparticles. The asymmetric shape of these composites was confirmed by TEM characterization. Moreover, characteristics of anisotropic surface functionalities were indicated by Zeta potential measurement and confocal laser microscopy after being labeled with fluorescent dyes. This structure could find potential use as carriers for biological applications.

  17. Fluid and ionic transport properties of deformed salt rock

    International Nuclear Information System (INIS)

    This is a final report on work done on the transport properties of salt during the period 1 January 1984 to 30 June 1985. This work was directed largely at the measurement of creep-induced permeability in salt rock, at determining the permeability persistence/decay characteristics of creep-dilated salt rock under hydrostatic conditions, and at ion migration/retention experiments on both deformed and undeformed material. The permeability work was carried out using both gas (argon) and brine, and involved the design and construction of corresponding permeametry systems for use in conjunction with dilatometric triaxial testing apparatus. Ion migration/retention studies involved the use of contaminant species such as Sr2+, Cs+, Fe3+ and TcO4

  18. Energetic Salts Based on Tetrazole N-Oxide.

    Science.gov (United States)

    He, Piao; Zhang, Jian-Guo; Yin, Xin; Wu, Jin-Ting; Wu, Le; Zhou, Zun-Ning; Zhang, Tong-Lai

    2016-06-01

    Energetic materials (explosives, propellants, and pyrotechnics) are used extensively for both civilian and military applications and the development of such materials, particularly in the case of energetic salts, is subject to continuous research efforts all over the world. This Review concerns recent advances in the syntheses, properties, and potential applications of ionic salts based on tetrazole N-oxide. Most of these salts exhibit excellent characteristics and can be classified as a new family of highly energetic materials with increased density and performance, alongside decreased mechanical sensitivity. Additionally, novel tetrazole N-oxide salts are proposed based on a diverse array of functional groups and ions pairs, which may be promising candidates for new energetic materials. PMID:27061423

  19. Promotion of radiation-induced cationic polymerization by onium salts

    International Nuclear Information System (INIS)

    The radiation-induced cationic polymerization of styrene derivatives was studied in the presence of diphenyliodonium and triphenylsulfonium hexafluorophosphates in dichloromethane. A remarkable promotion of the polymerization was observed in the presence of the salts. The pulse radiolysis study revealed that the promotion of the polymerization is due to the ion-pair formation between the initiating cations and the nonnucleophilic complex metal halide anions of the salts resulting in the stabilization of the cations toward neutralization. An additional effect observed in the case of diphenyliodonium salt is the oxidation of free radical species to the cations responsible for the polymerization. An increase in molecular weight at low temperature suggested that the propagating cations are also paired with the counterions derived from the salts. (author)

  20. Putting in evidence the asymmetric fission in the desexcitation process of 47V nuclei

    International Nuclear Information System (INIS)

    The fusion-fission, which reflects the instability of the nuclei against the deformation and leads to a binary break up into nearly equal mass nuclei, have been considered as a general feature of the heavy ions (A>80). For lighter systems the fission decay of the compound nucleus is predicted by the rotating liquid drop model to be minor process and the fully-damped products observed in reactions between light heavy ions (A35 Cl+12 C, 31 P+16 O and 23 Na+24 Mg reactions used in order to populate the 47 V system at two excitation energies E = 59 and 64 MeV. This study shows that these fragments are the result of the emission from a source and their elemental distributions are asymmetric independently to the entrance channel asymmetry. The absence of entrance channel effect is a signature of the asymmetric fission process of the 47 V nucleus. The comparison of the experimental observations to the statistical model shows that the fission barriers in this mass region are lower than those predicted by the rotating liquid drop model and the need of introducing their angular momentum and mass asymmetry dependence is clearly shown. In conclusion, it is well established that the evidence of the asymmetric fission break up into the desexcitation process of the 47 V nucleus should be taken into account in the statistical calculations describing the complete fusion of light heavy ions

  1. Salt acclimation processes in wheat.

    Science.gov (United States)

    Janda, Tibor; Darko, Éva; Shehata, Sami; Kovács, Viktória; Pál, Magda; Szalai, Gabriella

    2016-04-01

    Young wheat plants (Triticum aestivum L. cv. Mv Béres) were exposed to 0 or 25 mM NaCl for 11 days (salt acclimation). Thereafter the plants were irrigated with 500 mM NaCl for 5 days (salt stress). Irrigating the plants with a low concentration of NaCl successfully led to a reduction in chlorotic symptoms and in the impairment of the photosynthetic processes when the plants were exposed to subsequent high-dose salt treatment. After exposure to a high concentration of NaCl there was no difference in leaf Na content between the salt-acclimated and non-acclimated plants, indicating that salt acclimation did not significantly modify Na transport to the shoots. While the polyamine level was lower in salt-treated plants than in the control, salt acclimation led to increased osmotic potential in the leaves. Similarly, the activities of certain antioxidant enzymes, namely glutathione reductase, catalase and ascorbate peroxidase, were significantly higher in salt-acclimated plants. The results also suggest that while SOS1, SOS2 or NHX2 do not play a decisive role in the salt acclimation processes in young wheat plants; another stress-related gene, WALI6, may contribute to the success of the salt acclimation processes. The present study suggested that the responses of wheat plants to acclimation with low level of salt and to treatment with high doses of salt may be fundamentally different. PMID:26854409

  2. Asymmetric membrane osmotic capsules for terbutaline sulphate

    Directory of Open Access Journals (Sweden)

    N G Gobade

    2012-01-01

    Full Text Available The aim of the present study was to design an asymmetric membrane capsule, an osmotic pump-based drug delivery system of ethyl cellulose for controlled release of terbutaline sulphate. asymmetric membrane capsules contains pore-forming water soluble additive, sorbitol in different concentrations in the capsule shell membrane, which after coming in contact with water, dissolves, resulting in an in situ formation of a microporous structure. The terbutaline sulphate is a β-adrenoreceptor agonist widely used in the treatment of asthma. The oral dosage regimen of terbutaline sulphate is 5 mg twice or thrice daily, the plasma half-life is approximate 3-4 h and it produces GI irritation with extensive first pass metabolism. Hence, terbutaline sulphate was chosen as a model drug with an aim to develop controlled release system. Different formulations of ethyl cellulose were prepared by phase inversion technique using different concentrations of sorbitol as pore forming agent. It was found that the thickness of the prepared asymmetric membrane capsules was increased with increase in concentration of ethyl cellulose and pore forming agent, i.e. sorbitol. The dye release study in water and 10% sodium chloride solution indicates that, the asymmetric membrane capsules follow osmotic principle to release content. The pores formed due to sorbitol were confirmed by microscopic observation of transverse section of capsule membrane. Data of in vitro release study of terbutaline sulphate from asymmetric membrane capsules indicated that, the capsules prepared with 10% and 12.5% of ethyl cellulose and 25% of sorbitol released as much as 97.44% and 76.27% in 12 h, respectively with zero order release rate. Hence asymmetric membrane capsule of 10% ethyl cellulose and 25% of sorbitol is considered as optimum for controlled oral delivery of terbutaline sulphate.

  3. Asymmetric membrane osmotic capsules for terbutaline sulphate.

    Science.gov (United States)

    Gobade, N G; Koland, Marina; Harish, K H

    2012-01-01

    The aim of the present study was to design an asymmetric membrane capsule, an osmotic pump-based drug delivery system of ethyl cellulose for controlled release of terbutaline sulphate. asymmetric membrane capsules contains pore-forming water soluble additive, sorbitol in different concentrations in the capsule shell membrane, which after coming in contact with water, dissolves, resulting in an in situ formation of a microporous structure. The terbutaline sulphate is a β-adrenoreceptor agonist widely used in the treatment of asthma. The oral dosage regimen of terbutaline sulphate is 5 mg twice or thrice daily, the plasma half-life is approximate 3-4 h and it produces GI irritation with extensive first pass metabolism. Hence, terbutaline sulphate was chosen as a model drug with an aim to develop controlled release system. Different formulations of ethyl cellulose were prepared by phase inversion technique using different concentrations of sorbitol as pore forming agent. It was found that the thickness of the prepared asymmetric membrane capsules was increased with increase in concentration of ethyl cellulose and pore forming agent, i.e. sorbitol. The dye release study in water and 10% sodium chloride solution indicates that, the asymmetric membrane capsules follow osmotic principle to release content. The pores formed due to sorbitol were confirmed by microscopic observation of transverse section of capsule membrane. Data of in vitro release study of terbutaline sulphate from asymmetric membrane capsules indicated that, the capsules prepared with 10% and 12.5% of ethyl cellulose and 25% of sorbitol released as much as 97.44% and 76.27% in 12 h, respectively with zero order release rate. Hence asymmetric membrane capsule of 10% ethyl cellulose and 25% of sorbitol is considered as optimum for controlled oral delivery of terbutaline sulphate. PMID:23204625

  4. Quantitative Analysis of Soil Salt and Its Main Ions Based on Visible/Near Infrared Spectroscopy in Estuary Area of Yellow River%基于可见/近红外光谱的黄河口区土壤盐分及其主要离子的定量分析

    Institute of Scientific and Technical Information of China (English)

    刘亚秋; 陈红艳; 王瑞燕; 常春艳; 陈哲

    2016-01-01

    Objective]It is crucial to quantitatively and accurately detect saline soil for the prevention of soil salinization and agricultural sustainable development. The objective of this study is to find the characteristic spectra of soil salt and its main ions, and build a quantitative analysis model of soil salinization which is suitable for the estuary area of Yellow River to improve the accuracy and stability of the quantitative analysis. [Method] Kenli County in Shandong Province was selected as the experimental area. Firstly, 96 representative soil samples were collected on October 5th-9th, 2014. After soil sample were dried, the contents of soil salt and ions were analyzed. Then the visible and near infrared reflectance hyperspectra of the soil samples were measured in the laboratory by ASD Fieldspec 3 spectrometer, smoothed and transformed to the first deviation. Secondly, the response spectra of salt and its main ions (Cl-, Na+, Ca2+)were analyzed, first soil salinity and main ions content and the first derivative spectra of reflectance by band correlation analysis, according to the principle of correlation coefficient and significant, their sensitive bands were selected as the characteristic bands, feature bands with maximum correlation coefficient were chosen as the significant feature bands. Then the characteristic spectra which can represent soil salt and main ions (Cl-, Na+, Ca2+) were analyzed synthetically using correlation analysis and identified. Finally, the methods of multiple linear regression (MLR), support vector machine (SVM) and random forest (RF) were used respectively to build quantitative analysis models of soil salinity and ions contents. [Result] The overall shape and trend of the spectra curves of soil salinity and major ions (Cl-, Na+, Ca2+) content in study area were very similar. Soil salinity and major ions (Cl-, Na+, Ca2+) spectra response regions were determined to be 1 320-1 495, 1 790-1 920, 2 120-2 290 nm. On account of the

  5. Algebraic Davis Decomposition and Asymmetric Doob Inequalities

    Science.gov (United States)

    Hong, Guixiang; Junge, Marius; Parcet, Javier

    2016-04-01

    In this paper we investigate asymmetric forms of Doob maximal inequality. The asymmetry is imposed by noncommutativity. Let {({M}, τ)} be a noncommutative probability space equipped with a filtration of von Neumann subalgebras {({M}_n)_{n ≥ 1}} , whose union {bigcup_{n≥1}{M}_n} is weak-* dense in {{M}} . Let {{E}_n} denote the corresponding family of conditional expectations. As an illustration for an asymmetric result, we prove that for {1 algebraic atomic description for the involved Hardy spaces. The latter results are new even for commutative von Neumann algebras.

  6. Improved DFIG Capability during Asymmetrical Grid Faults

    DEFF Research Database (Denmark)

    Zhou, Dao; Blaabjerg, Frede

    In the wind power application, different asymmetrical types of the grid fault can be categorized after the Y/d transformer, and the positive and negative components of a single-phase fault, phase-to-phase fault, and two-phase fault can be summarized. Due to the newly introduced negative and even......, the capability of a 2 MW DFIG to ride through asymmetrical grid faults can be estimated at the existing design of the power electronics converter. Finally, a control scheme aimed to improve the DFIG capability is proposed and the simulation results validate its feasibility....

  7. Hot and flowing, asymmetric nuclear matter

    International Nuclear Information System (INIS)

    We develop a consistent treatment for hot and flowing asymmetric nuclear matter. Using the mean-field theory, predictions of the σ- ω Walecka model at finite temperature are compared with the corresponding results of the Zimanyi-Moszlowski and the non-linear models. The statistical theory of grand-canonical potentials is incorporated to the formalism. We also describe the behavior, at finite temperature, of the asymmetric and flowing nuclear matter. As an application, we describe bulk properties of neutron and protoneutron stars by considering the Tolman-Oppenheimer-Volkoff equations. (author)

  8. Asymmetric acoustic transmission in multiple frequency bands

    International Nuclear Information System (INIS)

    We report both experimentally and numerically that the multi-band device of the asymmetric acoustic transmission is realized by placing two periodic gratings with different periods on both sides of two brass plates immersed in water. The asymmetric acoustic transmission can exist in four frequency bands below 1500 kHz, which arises from the interaction between various diffractions from the two gratings and Lamb modes in the brass plates immersed in water. The results indicate that the device has the advantages of multiple band, broader bandwidth, and simpler structure. Our finding should have great potential applications in ultrasonic devices

  9. Quiz: What's the Buzz about Salt?

    Science.gov (United States)

    ... on. Feature: Too Much Salt Quiz: What's the buzz about salt? Past Issues / Spring - Summer 2010 Table ... Thing / Labels: For your health / Quiz: What's the buzz about salt? / Tasty Stand-Ins for Salt Spring / ...

  10. Salt Contribution to the Flexibility of Single-stranded Nucleic Acid of Finite Length

    CERN Document Server

    Wang, Feng-Hua; Tan, Zhi-Jie

    2012-01-01

    Nucleic acids are negatively charged macromolecules and their structure properties are strongly coupled to metal ions in solutions. In this paper, the salt effects on the flexibility of single stranded (ss) nucleic acid chain ranging from 12 to 120 nucleotides are investigated systematically by the coarse grained Monte Carlo simulations where the salt ions are considered explicitly and the ss chain is modeled with the virtual bond structural model. Our calculations show that, the increase of ion concentration causes the structural collapse of ss chain and multivalent ions are much more efficient in causing such collapse, and trivalent and small divalent ions can both induce more compact state than a random relaxation state. We found that monovalent, divalent and trivalent ions can all overcharge ss chain, and the dominating source for such overcharging changes from ion exclusion volume effect to ion Coulomb correlations. In addition, the predicted Na and Mg dependent persistence length lp of ss nucleic acid a...

  11. Performance and cost characteristics of multi-electron transfer, common ion exchange non-aqueous redox flow batteries

    Science.gov (United States)

    Laramie, Sydney M.; Milshtein, Jarrod D.; Breault, Tanya M.; Brushett, Fikile R.; Thompson, Levi T.

    2016-09-01

    Non-aqueous redox flow batteries (NAqRFBs) have recently received considerable attention as promising high energy density, low cost grid-level energy storage technologies. Despite these attractive features, NAqRFBs are still at an early stage of development and innovative design techniques are necessary to improve performance and decrease costs. In this work, we investigate multi-electron transfer, common ion exchange NAqRFBs. Common ion systems decrease the supporting electrolyte requirement, which subsequently improves active material solubility and decreases electrolyte cost. Voltammetric and electrolytic techniques are used to study the electrochemical performance and chemical compatibility of model redox active materials, iron (II) tris(2,2‧-bipyridine) tetrafluoroborate (Fe(bpy)3(BF4)2) and ferrocenylmethyl dimethyl ethyl ammonium tetrafluoroborate (Fc1N112-BF4). These results help disentangle complex cycling behavior observed in flow cell experiments. Further, a simple techno-economic model demonstrates the cost benefits of employing common ion exchange NAqRFBs, afforded by decreasing the salt and solvent contributions to total chemical cost. This study highlights two new concepts, common ion exchange and multi-electron transfer, for NAqRFBs through a demonstration flow cell employing model active species. In addition, the compatibility analysis developed for asymmetric chemistries can apply to other promising species, including organics, metal coordination complexes (MCCs) and mixed MCC/organic systems, enabling the design of low cost NAqRFBs.

  12. A study of salt effects on the complexation between beta-cyclodextrins and bile salts based on the Hofmeister series

    DEFF Research Database (Denmark)

    Holm, Rene; Schonbeck, Christian; Somprasirt, Pitchayanun;

    2014-01-01

    bound drug molecules. The influence of Hofmeister ions on the binding constants of complexes between CDs (β-CD and hydroxypropylated β-CD) and bile salts (glycocholate and glycochenodeoxycholate) were examined by isothermal titration calorimetry. The chaotropic anions tended to weaken these inclusion...

  13. Mixed salt crystallisation fouling

    CERN Document Server

    Helalizadeh, A

    2002-01-01

    The main purpose of this investigation was to study the mechanisms of mixed salt crystallisation fouling on heat transfer surfaces during convective heat transfer and sub-cooled flow boiling conditions. To-date no investigations on the effects of operating parameters on the deposition of mixtures of calcium sulphate and calcium carbonate, which are the most common constituents of scales formed on heat transfer surfaces, have been reported. As part of this research project, a substantial number of experiments were performed to determine the mechanisms controlling deposition. Fluid velocity, heat flux, surface and bulk temperatures, concentration of the solution, ionic strength, pressure and heat transfer surface material were varied systematically. After clarification of the effect of these parameters on the deposition process, the results of these experiments were used to develop a mechanistic model for prediction of fouling resistances, caused by crystallisation of mixed salts, under convective heat transfer...

  14. Frost formation with salt

    OpenAIRE

    Guadarrama-Cetina, J.; Mongruel, A. (Anne); González-Viñas, W.; Beysens, D.A. (Daniel A.)

    2015-01-01

    The formation of frost in presence of salt (NaCl) crystal is experimentally investigated on a hydrophobic surface. It presents several remarkable features due to the interplay of salty-water saturation pressure evolution, initially lower than the saturation pressure of ice and water, and the percolating propagation of ice dendrites from defects throughout the supercooled water droplet pattern. In particular, it is remarkable that nucleation of supercooled water and/or ice is prevented around ...

  15. Study of the energy inventory during asymmetric magnetic reconnection in a laboratory plasma

    Science.gov (United States)

    Yoo, Jongsoo; Yamada, Masaaki; Na, Ben; Jara-Almonte, Jonathan; Ji, Hantao; Fox, Will; Chien, Abe

    2015-11-01

    The energy inventory of a magnetic reconnection layer is studied in a laboratory plasma with a significant density asymmetry across the current sheet. The upstream density ratio of about 7 is generated by the in-plane inductive electric field during the plasma formation in MRX. Compared to the symmetric case where the ion energy gain is about twice more than that of electrons, the ion energy gain becomes smaller and the electron energy gain is larger. The reduction in the ion energy gain is mainly caused by the asymmetric profile of the in-plane electrostatic potential, which is generated to balance the Lorentz force in the electron momentum equation. Since the out-of-plane electron fluid velocity on the high-density side is small due to the high density, the potential drop on the high-density side becomes also small. The potential drop on the low-density side is also smaller than expected from the general scaling (~B2 / n), since it is suppressed by a large density gradient across the low-density side separatrices. As a result, the ion energy gain from the in-plane electrostatic field is smaller than the symmetric case, thereby decreasing the total ion energy gain. Discussion on the electron energization process during asymmetric reconnection is also presented. This research is supported by DoE Contract Number DE-AC02-09CH11466.

  16. Preconceptual design of a salt splitting process using ceramic membranes

    Energy Technology Data Exchange (ETDEWEB)

    Kurath, D.E.; Brooks, K.P.; Hollenberg, G.W.; Clemmer, R. [Pacific Northwest National Lab., Richland, WA (United States); Balagopal, S.; Landro, T.; Sutija, D.P. [Ceramatec, Inc., Salt Lake City, UT (United States)

    1997-01-01

    Inorganic ceramic membranes for salt splitting of radioactively contaminated sodium salt solutions are being developed for treating U. S. Department of Energy tank wastes. The process consists of electrochemical separation of sodium ions from the salt solution using sodium (Na) Super Ion Conductors (NaSICON) membranes. The primary NaSICON compositions being investigated are based on rare- earth ions (RE-NaSICON). Potential applications include: caustic recycling for sludge leaching, regenerating ion exchange resins, inhibiting corrosion in carbon-steel tanks, or retrieving tank wastes; reducing the volume of low-level wastes volume to be disposed of; adjusting pH and reducing competing cations to enhance cesium ion exchange processes; reducing sodium in high-level-waste sludges; and removing sodium from acidic wastes to facilitate calcining. These applications encompass wastes stored at the Hanford, Savannah River, and Idaho National Engineering Laboratory sites. The overall project objective is to supply a salt splitting process unit that impacts the waste treatment and disposal flowsheets and meets user requirements. The potential flowsheet impacts include improving the efficiency of the waste pretreatment processes, reducing volume, and increasing the quality of the final waste disposal forms. Meeting user requirements implies developing the technology to the point where it is available as standard equipment with predictable and reliable performance. This report presents two preconceptual designs for a full-scale salt splitting process based on the RE-NaSICON membranes to distinguish critical items for testing and to provide a vision that site users can evaluate.

  17. Preconceptual design of a salt splitting process using ceramic membranes

    International Nuclear Information System (INIS)

    Inorganic ceramic membranes for salt splitting of radioactively contaminated sodium salt solutions are being developed for treating U. S. Department of Energy tank wastes. The process consists of electrochemical separation of sodium ions from the salt solution using sodium (Na) Super Ion Conductors (NaSICON) membranes. The primary NaSICON compositions being investigated are based on rare- earth ions (RE-NaSICON). Potential applications include: caustic recycling for sludge leaching, regenerating ion exchange resins, inhibiting corrosion in carbon-steel tanks, or retrieving tank wastes; reducing the volume of low-level wastes volume to be disposed of; adjusting pH and reducing competing cations to enhance cesium ion exchange processes; reducing sodium in high-level-waste sludges; and removing sodium from acidic wastes to facilitate calcining. These applications encompass wastes stored at the Hanford, Savannah River, and Idaho National Engineering Laboratory sites. The overall project objective is to supply a salt splitting process unit that impacts the waste treatment and disposal flowsheets and meets user requirements. The potential flowsheet impacts include improving the efficiency of the waste pretreatment processes, reducing volume, and increasing the quality of the final waste disposal forms. Meeting user requirements implies developing the technology to the point where it is available as standard equipment with predictable and reliable performance. This report presents two preconceptual designs for a full-scale salt splitting process based on the RE-NaSICON membranes to distinguish critical items for testing and to provide a vision that site users can evaluate

  18. Asymmetric cell division: a persistent issue?

    OpenAIRE

    Aakre, Christopher D.; Laub, Michael T.

    2012-01-01

    Heterogeneity within a clonal population of cells can increase survival in the face of environmental stress. In a recent issue of Science, Aldridge et al. (2012) demonstrate that cell division in mycobacteria is asymmetric, producing daughter cells that differ in size, growth rate, and susceptibility to antibiotics.

  19. Asymmetric demand for energy: A cointegration approach

    Science.gov (United States)

    Maclean, Thomas Frank

    1997-12-01

    This paper uses time series data in a study of the demand for energy. One goal is to compare the results from the traditional autoregressive distributed lag (ADL) model to the error correction model (ECM) using cointegration. The second goal is to determine if the demand elasticity is asymmetric with respect to increasing and decreasing prices. This paper discusses three topics that are important to the use of time series data. The first topic is the presence and consequences unit roots which are common in time series data. The second topic is the identification of cointegrated variables and the third topic is a development of the ECM. This results in a model that can be used in either a single equation or multivariate system context and it will estimate both long run and short run elasticities. Asymmetry theory and its implications are studied along with an investigation into competing methods of creating the asymmetric variables. Simulations provided evidence that the use of dummy variables results in biased estimates and that the cumulative difference method of Wolffram/Houck gives valid estimates. The results of the empirical part of the paper show that the short run estimates of the ADL model are like those of the error correction model, but the cointegration method's long run estimates are better since they are known to be consistent and asymptotically unbiased. Tests for asymmetry do not support the theory of asymmetric long run price elasticities; however there is evidence to support the presence of asymmetric demand in the short run.

  20. Leverage bounds with default and asymmetric information

    Czech Academy of Sciences Publication Activity Database

    Boháček, Radim

    2014. [2014 North American Summer Meeting of the Econometric Society. Minneapolis (US), 19.06.2014-22.06.2014] R&D Projects: GA ČR GA402/09/1340 Institutional support: RVO:67985998 Keywords : financial markets and the macroeconomy * asymmetric and private information * occupational choice Subject RIV: AH - Economics http://editorialexpress.com/conference/NASM2014/program/NASM2014.html

  1. Asymmetric Taxation under Incremental and Sequential Investment

    OpenAIRE

    Panteghini, Paolo

    2002-01-01

    This article discusses the effects of an asymmetric tax scheme on incremental and sequential investment strategies. The tax base is equal to the firm’s return, net of an imputation rate. When the firm’s return is less than this rate, however, no tax refunds are allowed. This scheme is neutral under both income and capital uncertainty.

  2. Beam-beam issues in asymmetric colliders

    Energy Technology Data Exchange (ETDEWEB)

    Furman, M.A.

    1992-07-01

    We discuss generic beam-beam issues for proposed asymmetric e{sup +}- e{sup -} colliders. We illustrate the issues by choosing, as examples, the proposals by Cornell University (CESR-B), KEK, and SLAC/LBL/LLNL (PEP-II).

  3. Catalytic asymmetric synthesis of mycocerosic acid

    NARCIS (Netherlands)

    ter Horst, B.; Feringa, B.L.; J. Minnaard, A.

    2007-01-01

    The first catalytic asymmetric total synthesis of mycocerosic acid was achieved via the application of iterative enantioselective 1,4-addition reactions and allows for the efficient construction of 1,3-polymethyl arrays with full stereocontrol; further exemplified by the synthesis of tetramethyl-dec

  4. Evidence of asymmetric top in 130Ba

    International Nuclear Information System (INIS)

    Introduced is a new relation connecting moment of inertia, Lipas parameter and asymmetric rotor model energies and put forward much closer trend in odd even staggering of quasi γ-band. A different view point regarding generation of quasi γ-band in 130Ba have been presented

  5. Asymmetric conditional volatility in international stock markets

    Science.gov (United States)

    Ferreira, Nuno B.; Menezes, Rui; Mendes, Diana A.

    2007-08-01

    Recent studies show that a negative shock in stock prices will generate more volatility than a positive shock of similar magnitude. The aim of this paper is to appraise the hypothesis under which the conditional mean and the conditional variance of stock returns are asymmetric functions of past information. We compare the results for the Portuguese Stock Market Index PSI 20 with six other Stock Market Indices, namely the SP 500, FTSE 100, DAX 30, CAC 40, ASE 20, and IBEX 35. In order to assess asymmetric volatility we use autoregressive conditional heteroskedasticity specifications known as TARCH and EGARCH. We also test for asymmetry after controlling for the effect of macroeconomic factors on stock market returns using TAR and M-TAR specifications within a VAR framework. Our results show that the conditional variance is an asymmetric function of past innovations raising proportionately more during market declines, a phenomenon known as the leverage effect. However, when we control for the effect of changes in macroeconomic variables, we find no significant evidence of asymmetric behaviour of the stock market returns. There are some signs that the Portuguese Stock Market tends to show somewhat less market efficiency than other markets since the effect of the shocks appear to take a longer time to dissipate.

  6. Detection loophole in asymmetric Bell experiments

    OpenAIRE

    Brunner, Nicolas; Gisin, Nicolas; Scarani, Valerio; Simon, Christoph

    2007-01-01

    The problem of closing the detection loophole with asymmetric systems, such as entangled atom-photon pairs, is addressed. We show that, for the Bell inequality I_3322, a minimal detection efficiency of 43% can be tolerated for one of the particles, if the other one is always detected. We also study the influence of noise and discuss the prospects of experimental implementation.

  7. Standards vs. labels with imperfect competition and asymmetric information

    DEFF Research Database (Denmark)

    Baltzer, Kenneth Thomas

    2012-01-01

    I demonstrate that providing information about product quality is not necessarily the best way to address asymmetric information problems when markets are imperfectly competitive. In a vertical differentiation model I show that a Minimum Quality Standard, which retains asymmetric information...

  8. Standards vs. labels with imperfect competition and asymmetric information

    DEFF Research Database (Denmark)

    Baltzer, Kenneth Thomas

    I demonstrate that providing information about product quality is not necessarily the best way to address asymmetric information problems when markets are imperfectly competitive. In a vertical dierentiation model I show that a Minimum Quality Standard, which retains asymmetric information...

  9. Asymmetric Bulkheads for Cylindrical Pressure Vessels

    Science.gov (United States)

    Ford, Donald B.

    2007-01-01

    Asymmetric bulkheads are proposed for the ends of vertically oriented cylindrical pressure vessels. These bulkheads, which would feature both convex and concave contours, would offer advantages over purely convex, purely concave, and flat bulkheads (see figure). Intended originally to be applied to large tanks that hold propellant liquids for launching spacecraft, the asymmetric-bulkhead concept may also be attractive for terrestrial pressure vessels for which there are requirements to maximize volumetric and mass efficiencies. A description of the relative advantages and disadvantages of prior symmetric bulkhead configurations is prerequisite to understanding the advantages of the proposed asymmetric configuration: In order to obtain adequate strength, flat bulkheads must be made thicker, relative to concave and convex bulkheads; the difference in thickness is such that, other things being equal, pressure vessels with flat bulkheads must be made heavier than ones with concave or convex bulkheads. Convex bulkhead designs increase overall tank lengths, thereby necessitating additional supporting structure for keeping tanks vertical. Concave bulkhead configurations increase tank lengths and detract from volumetric efficiency, even though they do not necessitate additional supporting structure. The shape of a bulkhead affects the proportion of residual fluid in a tank that is, the portion of fluid that unavoidably remains in the tank during outflow and hence cannot be used. In this regard, a flat bulkhead is disadvantageous in two respects: (1) It lacks a single low point for optimum placement of an outlet and (2) a vortex that forms at the outlet during outflow prevents a relatively large amount of fluid from leaving the tank. A concave bulkhead also lacks a single low point for optimum placement of an outlet. Like purely concave and purely convex bulkhead configurations, the proposed asymmetric bulkhead configurations would be more mass-efficient than is the flat

  10. Burn-off dominated uranium and asymmetric copper-gold operation in RHIC

    Science.gov (United States)

    Luo, Y.; Fischer, W.; Blaskiewicz, M.; Brennan, J. M.; Kling, N.; Mernick, K.; Roser, T.

    2014-08-01

    In 2012 the Relativistic Heavy Ion Collider collided uranium-uranium ions with a particle energy of 96.4 GeV/nucleon and copper-gold (Cu-Au) ions at 100 GeV/nucleon for the first time. 3-dimensional stochastic cooling became operational for the first time and greatly enhanced the luminosity. Together with a new lattice configuration, we achieved a burn-off dominated uranium beam lifetime at physics stores. In the asymmetric Cu-Au collision, we observed an increased Cu beam loss stemming from different intrabeam-scattering and cooling rates between the Au and Cu ion bunches. By intentionally slowing down the cooling rate for the Au beam at the beginning of store, we reduced the Cu beam loss and maximized the integrated luminosity.

  11. Separation of actinides with alkylpyridinium salts

    International Nuclear Information System (INIS)

    Various f-elements are separated as anionic complexes from both acidic and alkaline solutions by precipitation with alkylpyridinium salts. The precipitates are also cationic surfactants where the simple counter-ion (e.g. nitrate or chloride) is replaced by the negatively charged complex anion of an actinide or lanthanide. The low solubility of these precipitates is explained by a strong affinity of divalent complex counter-ions of f-elements to the quaternary nitrogen. Precipitations in solutions of nitric acid allow to separate tetravalent f-elements from other metals, in alkaline carbonate solutions tetravalent and hexavalent actinides are precipitated simultaneously. The last procedure yields precipitates, which are very intimate mixtures of hexavalent and tetravalent actinides. This allows to prepare mixed oxides in a simple way. (author) 6 refs.; 3 figs.; 3 tabs

  12. Americium separations from high salt solutions

    International Nuclear Information System (INIS)

    Americium (III) exhibits an unexpectedly high affinity for anion-exchange material from the high-salt evaporator bottoms solutions--an effect which has not been duplicated using simple salt solutions. Similar behavior is observed for its lanthanide homologue, Nd(III), in complex evaporator bottoms surrogate solutions. There appears to be no single controlling factor--acid concentration, total nitrate concentration or solution ionic strength--which accounts for the approximately 2-fold increase in retention of the trivalent ions from complex solutions relative to simple solutions. Calculation of species activities (i.e., water, proton and nitrate) in such concentrated mixed salt solutions is difficult and of questionable accuracy, but it is likely that the answer to forcing formation of anionic nitrate complexes of americium lies in the relative activities of water and nitrate. From a practical viewpoint, the modest americium removal needs (ca. 50--75%) from nitric acid evaporator bottoms allow sufficient latitude for the use of non-optimized conditions such as running existing columns filled with older, well-used Reillex HPQ. Newer materials, such as HPQ-100 and the experimental bifunctional resins, which exhibit higher distribution coefficients, would allow for either increased Am removal or the use of smaller columns. It is also of interest that one of the experimental neutral-donor solid-support extractants, DHDECMP, exhibits a similarly high level of americium (total alpha) removal from EV bottoms and is much less sensitive to total acid content than commercially-available material

  13. Thermal phase behaviour of N-alkyl-N-methylpyrrolidinium and piperidinium bis(trifluoromethanesulfonyl)imide salts

    International Nuclear Information System (INIS)

    The phases, ion crystal packing and thermal properties of the N-alkyl-N-methylpyrrolidinium and piperidinium bis(trifluoromethanesulfonyl)imide (PYR1RTFSI and PIP1RTFSI (subscript R = 1 for methyl and 2 for ethyl), respectively) salts are compared using powder and single-crystal x-ray diffraction (XRD) and differential scanning calorimetry (DSC). The crystal structure of PIP12TFSI has been determined at 123 K. The salt crystallizes in the triclinic space group P1-bar with Z 8. Structural data are also reported for PYR11TFSI at 153 K and PIP12TFSI at 223 K. PIP11TFSI has identical ion crystal packing to the analogous pyrrolidinium salt PYR11TFSI. Since increasing the cation alkyl chain length to propyl or butyl (R = 3 or 4) reduces the melting point of the salts below room temperature, this study may provide valuable insight into why these pyrrolidinium and piperidinium salts form room-temperature ionic liquids

  14. Asymmetric dual-gate tunneling FET with improved performance

    Science.gov (United States)

    Wang, Ying; Wang, Yan-fu; Xue, Wei; Cao, Fei

    2016-03-01

    In this work, we propose and simulate an asymmetric dual-gate tunneling FET (ADG-TFET) combining a tunneling field effect transistor (TFET) with a junctionless field effect transistor (JLFET). The current is controlled by an in the bottom channel potential barrier as well as the reverse-biased P+ pocket-Intrinsic region (p-i) tunnel junction bandgap, which combines the merits of both bandgap-controlled TFET and barrier-controlled JLFET. The simulation results of ADG-TFET with high-κ dielectric material (HfO2) of 40-nm gate length show excellent characteristics with high ION/IOFF ratio of 3.3 × 1010 and ION of 302 μA/μm, a steep subthreshold slope (SS) for point SS of 35 mV/decade and average SS of 54 mV/decade at room temperature, which indicates that ADG-TFET is a promising candidate for future low power circuit applications.

  15. Intrinsic momentum transport in up-down asymmetric tokamaks

    CERN Document Server

    Ball, Justin; Barnes, Michael; Dorland, William; Hammett, Gregory W; Rodrigues, Paulo; Loureiro, Nuno F

    2014-01-01

    Recent work demonstrated that breaking the up-down symmetry of tokamak flux surfaces removes a constraint that limits intrinsic momentum transport, and hence toroidal rotation, to be small. We show, through MHD analysis, that ellipticity is most effective at introducing up-down asymmetry throughout the plasma. We detail an extension to GS2, a local $\\delta f$ gyrokinetic code that self-consistently calculates momentum transport, to permit up-down asymmetric configurations. Tokamaks with tilted elliptical poloidal cross-sections were simulated to determine nonlinear momentum transport. The results, which are consistent with experiment in magnitude, suggest that a toroidal velocity gradient, $\\left( \\partial u_{\\zeta i} / \\partial \\rho \\right) / v_{th i}$, of 5% of the temperature gradient, $\\left(\\partial T_{i} / \\partial \\rho \\right) / T_{i}$, is sustainable. Here $v_{th i}$ is the ion thermal speed, $u_{\\zeta i}$ is the ion toroidal mean flow, $\\rho$ is the minor radial coordinate normalized to the tokamak m...

  16. Dynamics of salt playa polygons

    Science.gov (United States)

    Goehring, L.; Fourrière, A.

    2014-12-01

    In natural salt playa or in evaporation pools for the salt extraction industry, one can sometimes see surprising regular structures formed by ridges of salt. These ridges connect together to form a self-organized network of polygons one to two meters in diameter, which we call salt polygons. Here we propose a mechanism based on porous media convection of salty water in soil to explain the formation and the scaling of the salt polygons. Surface evaporation causes a steady upward flow of salty water, which can cause precipitation near the surface. A vertical salt gradient then builds up in the porous soil, with heavy salt-saturated water lying over the less salty source water. This can drive convection when a threshold is reached, given by a critical Rayleigh number of about 7. We suggest that the salt polygons are the surface expression of the porous medium convection, with salt crystallizing along the positions of the convective downwellings. To study this instability directly, we developed a 2D analogue experiment using a Hele-Shaw cell filled with a porous medium saturated with a salt solution and heated from above. We perform a linear stability analysis of this system, and find that it is unstable to convection, with a most unstable wavelength that is set by a balance between salt diffusion and water evaporation. The Rayleigh number in our experiment is controlled by the particle size of our model soil, and the evaporation rate. We obtain results that scale with the observation of natural salt polygons. Using dye, we observe the convective movement of salty water and find downwelling convective plumes underneath the spots where surface salt ridges form, as shown in the attached figure.

  17. Reactive halogen species above salt lakes and salt pans

    OpenAIRE

    Holla, Robert

    2013-01-01

    Salt lakes can be found on all continents and saline soils cover 2.5% of the land surface of the earth (FAO, 2012). This thesis investigates the presence of reactive halogen species (RHS) above salt lakes and saline soils to evaluate their relevance for tropospheric chemistry of the planetary boundary layer. Ground-based MAX-DOAS and LP-DOAS measurements were conducted at salt lakes and two other sites with high halogen content. Prior to this work, RHS were found at three salt ...

  18. NOx emissions and NO2- formation in thermal energy storage process of binary molten nitrate salts

    International Nuclear Information System (INIS)

    Referring to the national environmental protection standard of PR China, HJ479-2009, NOx emissions and the effect of 45# carbon steel (1045, ASTM) on it in thermal energy storage (TES) process of binary molten nitrate (BMN) salts (a eutectic salt mixture named as solar salt with the component of 60% NaNO3 and 40% KNO3) are discussed in this paper. The accumulative absorption concentrations of NOx emissions in tail gases of molten salts heated at different temperatures were measured to study the thermal decomposition situation of molten salts in TES process. Furthermore, the concentrations of nitrite ion in molten salts samples were determined and chemical thermodynamic calculations of related reactions were done to explain the results. The research shows that BMN salts contained in silica or carbon steel container in the air under certain conditions can release NOx in its use of temperature range. The concentrations of NOx emissions and nitrite ion in molten salts both increase with the rise of the temperature. After contacting with 45# carbon steel, the total concentrations of NOx emissions and nitrite ion in molten salts increased, which may be caused by Fe component in the carbon steel. - Highlights: • NOx emissions in TES process of binary molten nitrate salts are discussed. • The effect of 45# carbon steel on NOx emissions was also studied. • The concentrations of NOx emissions increase with the rise of the temperature. • The concentrations of nitrite ion creep with increasing temperature. • Fe element in the carbon steel may result in the increment of NO emissions

  19. Generic aspects of salt repositories

    International Nuclear Information System (INIS)

    The history of geological disposal of radioactive wastes in salt is presented from 1957 when a panel of the National Academy of Sciences-National Research Council recommended burial in bedded salt deposits. Early work began in the Kansas, portion of the Permian Basin where simulated wastes were placed in an abandoned salt mine at Lyons, Kansas, in the late 1960's. This project was terminated when the potential effect of nearby solution mining activities could not be resolved. Evaluation of bedded salts resumed a few years later in the Permian Basin in southeastern New Mexico, and search for suitable sites in the 1970's resulted in the formation of the National Waste Terminal Storage Program in 1976. Evaluation of salt deposits in many regions of the United States has been virtually completed and has shown that deposits having the greatest potential for radioactive waste disposal are those of the largest depositional basins and salt domes of the Gulf Coast region

  20. Modulation of collagen by addition of Hofmeister salts.

    Science.gov (United States)

    Oechsle, Anja Maria; Landenberger, Markus; Gibis, Monika; Irmscher, Stefan Björn; Kohlus, Reinhard; Weiss, Jochen

    2015-08-01

    Collagen can be modified by addition of chaotropic or kosmotropic salts of the reversed Hofmeister series. Hence, telopeptide-poor collagen type I was suspended in H2SO4 (pH 2) and 0.05-0.5 M KCl and KNO3 (chaotropes), as well as KI and KSCN (kosmotropes). Rheological parameters, including storage and loss modulus, intrinsic viscosity, and critical overlap concentration, were assessed and the microstructure was characterized by applying confocal laser scanning microscopy and scanning electron microscopy. The addition of up to 0.1 M KCl and 0.05 M KNO3 increased the intrinsic viscosity from 1.22 to 1.51 L/g without salt to a maximal value of 1.74 L/g and decreased the critical overlap concentration from 0.66 to 0.82 g/L to a minimal value of 0.57 g/L. Higher salt concentrations increased the collagen-collagen interactions due to ions withdrawing the water from the collagen molecules. Hence, 0.1 M KSCN delivered the largest structures with the highest structure factor, area value and the highest critical overlap concentration with 17.6 L/g. Overall, 0.5 M salt led to salting out, with chaotropes forming fine precipitates and kosmotropes leading to elastic three-dimensional networks. The study demonstrated that collagen entanglement and microstructure depend strongly on the ionic strength and type of salt. PMID:26014138