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Sample records for chloride ions determinacion

  1. Determination of the stability constants of lanthanum, praseodymium, europium, erbium and lutetium complexes with chloride ions; Determinacion de las constantes de estabilidad de los complejos de lantano, praseodimio, europio, erbio y lutecio con iones cloruro

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    Fernandez R, E. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)

    2008-07-01

    The stability constants of La{sup 3+}, Pr{sup 3+}, Eu{sup 3+}, Er{sup 3+} and Lu{sup 3+} chloride complexes were determined in perchloric acid media using a liquid-liquid extraction method. The dinonyl napthalene sulfonic acid in n-heptane was used as extractant. The lanthanide (Ln) concentrations were measured by a radiochemical (Eu and Lu) and a spectrophotometric (La, Pr, and Er) methods. In the last method, xylenol orange was used for the determinations at ph 6. The stability constants of lanthanum, praseodymium, erbium and lutetium chloride complexes were determined in 2, 3 and 4 M ionic strength and europium in 1, 2 and 3 M, at 303 K. The fitting of experimental data to the equations for the calculation of the stability constants, was carry out considering both one chemical species (LnCl{sup 2+}) or two chemical species (LnCl{sup 2+} and LnCl{sub 2}{sup +}). The Specific Ion Interaction Theory was applied to the values of log {beta}{sup I}{sub Ln},{sub Cl} and the first stability constants at zero ionic strength were calculated by extrapolation. The same theory could not be applied to the log {beta}{sup I}{sub Ln},{sub 2Cl}, due to its low abundance and the values determined for the stability constants were similar. The distribution diagrams of the chemical species were obtained using the program MEDUSA and considering log {beta}{sup I}{sub Ln},{sub CI}, log {beta}{sup I}{sub Ln},{sub 2CI} values obtained in this work and the hydrolysis constants taken from the literature. The lanthanide chloride complexes are present in solution at specific conditions of ionic strength, concentration and in the absence of hydrolysis. The log {beta}{sup I}{sub Ln},{sub Cl} data were related to the charge density and the corresponding equations were obtained. These equations could be used to determine the stability constants along the lanthanide series. (Author)

  2. Determination of lutetium (III) hydrolysis constants in the middle of ion force 1M sodium chloride at 303 K; Determinacion de las constantes de hidrolisis del lutecio (III), en medio de fuerza ionica 1M de cloruro de sodio, a 303 K

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    Jimenez R, M.; Solache R, M.J. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico); Ramirez G, J.J.; Rojas H, A. [Universidad Autonoma Metropolitana-Iztapalapa, Mexico D.F. (Mexico). Dept. de Quimica

    1997-07-01

    With the purpose to complete information about the lutetium (III) hydrolysis constants here is used the potentiometric method to determine those in the middle of ion force 1M sodium chloride at 303 K. (Author)

  3. Chloride Ion Critical Content in Reinforced Concrete

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Chloride ion critical content was studied under soaking and cycle of dry and wet conditions,with three electrochemical nondestructive measuring techniques, i e, half-cell potential, A C impedance, and time potential. The experimental results show that chloride ion critical content is primarily determined by the water cement ratio, while for the same concrete mixture the chloride ion critical content in soaking conditions is larger than that in a cycle of dry and wet conditions.

  4. Influence of Chloride-Ion Adsorption Agent on Chloride Ions in Concrete and Mortar

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    Gai-Fei Peng

    2014-04-01

    Full Text Available The influence of a chloride-ion adsorption agent (Cl agent in short, composed of zeolite, calcium aluminate hydrate and calcium nitrite, on the ingress of chloride ions into concrete and mortar has been experimentally studied. The permeability of concrete was measured, and the chloride ion content in mortar was tested. The experimental results reveal that the Cl agent could adsorb chloride ions effectively, which had penetrated into concrete and mortar. When the Cl agent was used at a dosage of 6% by mass of cementitious materials in mortar, the resistance to the penetration of chloride ions could be improved greatly, which was more pronounced when a combination of the Cl agent and fly ash or slag was employed. Such an effect is not the result of the low permeability of the mortar, but might be a result of the interaction between the Cl agent and the chloride ions penetrated into the mortar. There are two possible mechanisms for the interaction between the Cl agent and chloride ion ingress. One is the reaction between calcium aluminate hydrate in the Cl agent and chloride ions to form Friedel’s salt, and the other one is that calcium aluminate hydrate reacts with calcium nitrite to form AFm during the early-age hydration of mortar and later the NO2− in AFm is replaced by chloride ions, which then penetrate into the mortar, also forming Friedel’s salt. More research is needed to confirm the mechanisms.

  5. Dynamic Electrochemical Measurement of Chloride Ions.

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    Abbas, Yawar; de Graaf, Derk B; Olthuis, Wouter; van den Berg, Albert

    2016-02-05

    This protocol describes the dynamic measurement of chloride ions using the transition time of a silver silver chloride (Ag/AgCl) electrode. Silver silver chloride electrode is used extensively for potentiometric measurement of chloride ions concentration in electrolyte. In this measurement, long-term and continuous monitoring is limited due to the inherent drift and the requirement of a stable reference electrode. We utilized the chronopotentiometric approach to minimize drift and avoid the use of a conventional reference electrode. A galvanostatic pulse is applied to an Ag/AgCl electrode which initiates a faradic reaction depleting the Cl- ions near the electrode surface. The transition time, which is the time to completely deplete the ions near the electrode surface, is a function of the ion concentration, given by the Nernst equation. The square root of the transition time is in linear relation to the chloride ion concentration. Drift of the response over two weeks is negligible (59 µM/day) when measuring 1 mM [Cl-]using a current pulse of 10 Am(-2). This is a dynamic measurement where the moment of transition time determines the response and thus is independent of the absolute potential. Any metal wire can be used as a pseudo-reference electrode, making this approach feasible for long-term measurement inside concrete structures.

  6. Controlling chloride ions diffusion in concrete.

    Science.gov (United States)

    Zeng, Lunwu; Song, Runxia

    2013-11-28

    The corrosion of steel in concrete is mainly due to the chemical reaction between the chloride ions and iron ions. Indeed, this is a serious threaten for reinforced concrete structure, especially for the reinforced concrete structure in the sea. So it is urgent and important to protect concrete against chloride ions corrosion. In this work, we report multilayer concrete can cloak chloride ions. We formulated five kinds of concrete A, B, C, D and E, which are made of different proportion of cement, sand and glue, and fabricated six-layer (ABACAD) cylinder diffusion cloak and background media E. The simulation results show that the six-layer mass diffusion cloak can protect concrete against chloride ions penetration, while the experiment results show that the concentration gradients are parallel and equal outside the outer circle in the diffusion flux lines, the iso-concentration lines are parallel outside the outer circle, and the concentration gradients in the inner circle are smaller than those outside the outer circle.

  7. Amperometric Sensor for Detection of Chloride Ions

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    Rene Kizek

    2008-09-01

    Full Text Available Chloride ion sensing is important in many fields such as clinical diagnosis, environmental monitoring and industrial applications. We have measured chloride ions at a carbon paste electrode (CPE and at a CPE modified with solid AgNO3, a solution of AgNO3 and/or solid silver particles. Detection limits (3 S/N for chloride ions were 100 μM, 100 μM and 10 μM for solid AgNO3, solution of AgNO3 and/or solid silver particles, respectively. The CPE modified with silver particles is the most sensitive to the presence chloride ions. After that we approached to the miniaturization of the whole electrochemical instrument. Measurements were carried out on miniaturized instrument consisting of a potentiostat with dimensions 35 × 166 × 125 mm, screen printed electrodes, a peristaltic pump and a PC with control software. Under the most suitable experimental conditions (Britton-Robinson buffer, pH 1.8 and working electrode potential 550 mV we estimated the limit of detection (3 S/N as 500 nM.

  8. Magnesium anode for chloride ion batteries.

    Science.gov (United States)

    Zhao, Xiangyu; Li, Qiang; Zhao-Karger, Zhirong; Gao, Ping; Fink, Karin; Shen, Xiaodong; Fichtner, Maximilian

    2014-07-23

    A key advantage of chloride ion battery (CIB) is its possibility to use abundant electrode materials that are different from those in Li ion batteries. Mg anode is presented as such a material for the first time and Mg/C composite prepared by ball milling of Mg and carbon black powders or thermally decomposed MgH2/C composite has been tested as anode for CIB. The electrochemical performance of FeOCl/Mg and BiOCl/Mg was investigated, demonstrating the feasibility of using Mg as anode.

  9. Developing Polymer Cathode Material for the Chloride Ion Battery.

    Science.gov (United States)

    Zhao, Xiangyu; Zhao, Zhigang; Yang, Meng; Xia, Hui; Yu, Tingting; Shen, Xiaodong

    2017-01-25

    The chloride ion battery is an attractive rechargeable battery owing to its high theoretical energy density and sustainable components. An important challenge for research and development of chloride ion batteries lies in the innovation of the cathode materials. Here we report a nanostructured chloride ion-doped polymer, polypyrrole chloride, as a new type of potential cathode material for the chloride ion battery. The as-prepared polypyrrole chloride@carbon nanotubes (PPyCl@CNTs) cathode shows a high reversible capacity of 118 mAh g(-1) and superior cycling stability. Reversible electrochemical reactions of the PPyCl@CNTs cathode based on the redox reactions of nitrogen species and chloride ion transfer are demonstrated. Our work may guide and offer electrode design principles for accelerating the development of rechargeable batteries with anion transfer.

  10. Determination of the constants of the solubility product of Ln(OH){sub 3} and the effect of the chloride ions on the lanthanum hydrolysis, praseodymium and lutetium in aqueous solutions of ion force 2 Molar; Determinacion de las constantes del producto de solubilidad de Ln(OH){sub 3} y el efecto de los iones cloruro sobre la hidrolisis de lantano, praseodimio y lutecio en soluciones acuosas de fuerza ionica 2 Molar

    Energy Technology Data Exchange (ETDEWEB)

    Lopez G, H.D

    2005-07-01

    The behavior of lanthanum (III), praseodymium (III), and lutetium (III) was studied in 2 M NaClO{sub 4} (aq) and 2 M NaCl (aq) at 303 K and free -CO{sub 2} conditions. Solubility diagrams (p Ln(aq)-pC{sub H}) were obtained by means of a radiochemical method. The pC{sub H} borderlines of saturation and unsaturation zones of the solutions and solubility product constants for Ln(OH){sub 3} were determined from these diagrams. The fitting of the solubility equation to the experimental values of p Ln(aq)-pC{sub H} diagrams allowed the calculation of the first hydrolysis and solubility product constants. Independently, the stability constants for the first species of hydrolysis were determined by means of pH titrations, the data were treated with the program SUPERQUAD and fitted to the mean ligand number equation. The stability constants for the species LnCl{sup 2+} were as well calculated in 2M ionic strength and 303 K from the hydrolysis constant values obtained in both perchlorate and chloride media. The values obtained for La, Pr and Lu were: logK{sub ps}: 21.11 {+-} 0.09, 19.81 {+-} 0.11 and 18.10 {+-} 0.13 in 2M NaClO{sub 4}; logK{sub ps}: 22.22 {+-} 0.09, 21.45 {+-} 0.14 and 18.52 {+-} 0.29 in 2M NaCl; log {beta}{sub 1}: - 8.64 {+-} 0.02, - 8.37 {+-} 0.01 and - 7.95 {+-} 0.11 in 2M NaClO{sub 4}; log {beta}{sub 1}{sup /} : - 9.02 {+-} 0.11, - 8.75 {+-} 0.01 and - 8.12 {+-} 0.03 in 2M NaCl and the values for log {beta}{sub 1,Cl} were - 0.0255, - 0.155 and - 0.758, respectively. (Author)

  11. Ionometric determination of chloride ion in circulating and waste waters

    Energy Technology Data Exchange (ETDEWEB)

    Bebeshko, G.I.; Afanas' eva, V.I.; Danielova, I.I.; Dmitriev, M.A.; Radchenko, A.F.

    1986-09-01

    The authors attempt to develop selective ionometric methods to determine chloride ion in waste and circulating waters from technological ore processing, containing significant amounts of sulfide ion and various flotation reagents. These waters contain practically no cations that form hard to dissolve compounds with chloride ion such as Ag/sup +/, Cu/sup +/, Hg/sup +/ or Pb/sup 2 +/. The chloride ion concentration in water varies between 10 and 100 mg/liter. Information is shown on the concentration of the main anions and flotation reagents in waters that were analyzed.

  12. Chloride ion transport performance in slag mortar under fatigue loading

    Institute of Scientific and Technical Information of China (English)

    WANG CaiHui; SUN Wei; JIANG JinYang; HAN JianDe; YE BangTu

    2012-01-01

    The transport performance of chloride ion in slag cement mortar was investigated experimentally.In the self-designed experiment,fatigue loading was coupled simultaneously with ion transportation process,the diffusion law of chloride ion was obtained by titration and the AE (acoustic emission) technique was employed to detect the real-time damage distribution in the mortar specimen.The results for fatigue stress levels of 0.3,0.4 and 0.5 and slag contents of 0,10%,30% and 50% showed that fatigue loading accelerated the diffusion of chloride ion in mortar and the acceleration effect increased with the increase in stress levels.Slag addition was found to improve anti-chloride ion erosion performance effectively with the best substitution level at 30%,because the inhibition effect of slag on chloride ion diffusion diminished when the slag content exceeded 30%.The comparative experiments indicated that dynamic load has a significant effect on the transport performance of chloride ion in slag cement mortar.

  13. Effect of Chloride Type on Penetration of Chloride Ions in Concrete

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The influence of chloride type on the diffusivity of chloride ions in concrete was studied by experiment. The result shows that the glectric resistance of concrete and the chloride diffusion coefficient are influenced by chloride type. For the same water/cement ratio (W/C), the diffusion coefficient D in KCl solution is larger than that in NaCl solution; however, the concrete resistance in KCl solution is smaller than that in NaCl solution. The experimental result is analyzed with theory of diffusion.

  14. Determination of chloride in geological samples by ion chromatography

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    Wilson, S.A.; Gent, C.A.

    1983-01-01

    Samples of silicate rocks are prepared by sodium carbonate fusion and then treated by ion chromatography. The method was tested for geological standards with chloride concentration between 0.003 and 3%. Observed chloride concentrations comparedd favorably with literature values. The relative standard deviation and detection limit for the method were 8% and 7 ppm, respectively. Up to 30 determination per 24-hour period were possible. ?? 1983.

  15. The Influence of Mineral Functional Materials on Chloride Ion Penetration of Concrete

    Institute of Scientific and Technical Information of China (English)

    HU Hongmei; MA Baoguo

    2005-01-01

    The mechanism of chloride ion penetration in high performance concrete was analyzed. The experimental results indicate that there are two important reasons that influence the anti-chloride penetration of high performance concrete. One is the function effect of mineral functional material, so that it increases concrete's capability to resist chloride ion penetration. The other is combined action of mineral functional material's original capability of binding the chloride ion (physical adsorption) and physicochemical adsorption after hydration.

  16. Connecting to concrete: wireless monitoring of chloride ions in concrete structures

    NARCIS (Netherlands)

    Abbas, Yawar; Have, ten Bas; Hoekstra, Gerrit I.; Douma, Arjan; Bruijn, de Douwe; Olthuis, Wouter; Berg, van den Albert

    2015-01-01

    For the first time, chloride ions are measured wirelessly in concrete. The half-cell potential of a silver/silver chloride (Ag/AgCl) electrode, which corresponds to the concentration of chloride ions, is measured wirelessly. The sensor system (the Ag/AgCl and a reference electrode) is embedded in co

  17. Variable selectivity of the Hitachi chemistry analyzer chloride ion-selective electrode toward interfering ions.

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    Wang, T; Diamandis, E P; Lane, A; Baines, A D

    1994-02-01

    Chloride measurements by ion-selective electrodes are vulnerable to interference by anions such as iodide, thiocyanate, nitrate, and bromide. We have found that the degree of interference of these anions on the Hitachi chemistry analyzer chloride electrode varies from electrode to electrode and this variation can even occur within the same lot of membrane. This variation is not dependent upon the length of time the cartridge has been in the analyzer because no correlation existed between the usage time and the electrode response to interfering ions. Neither is this variation due to the deterioration of the electrode because all electrodes tested had calibration slopes within the manufacturer's specification. Our study, however, showed that even after repeated exposure to a plasma sample containing 2 mM thiocyanate, the chloride electrode was still able to accurately measure the chloride in plasma without thiocyanate, thus confirming that a carryover effect does not exist from a previous thiocyanate-containing sample.

  18. Effects of chloride and silver ions on gold nanorod formation

    Science.gov (United States)

    Ock Park, Jin; Cho, So-Hye; Jeong, Dae-Yong; Kong, Young-Min; Lee, Seung Yong

    2015-01-01

    The ability to tune the longitudinal localized surface plasmon resonance of gold nanorods (AuNRs) via simple modification of their aspect ratio is a large contributing factor to their widespread use across multiple fields. An understanding of the synthesis conditions that affect the aspect ratio and yield of AuNRs is therefore of utmost importance. From this perspective, we take a systematic approach in investigating the effect of the following conditions on the seed-mediated formation of AuNRs: the addition of chloride or silver ions, and the use of a hexadecyltrimethylammonium bromide (CTAB) source with different levels of effectiveness on controlling the shape of growing AuNRs.

  19. Effect of Nitrite Ions on Steel Corrosion Induced by Chloride or Sulfate Ions

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    Zhonglu Cao

    2013-01-01

    Full Text Available The influence of nitrite concentration on the corrosion of steel immersed in three simulated pH environments containing chloride ions or sulfate ions has been investigated by comparing and analyzing the change of half-cell potential, the change of threshold level of Cl- or SO42-, the change of threshold level of NO2-/Cl- or NO2-/SO42- mole ratio, and the changes of anodic/cathodic polarization curves and Stern-Geary constant B. The corrosivity of chloride ions against sulfate ions also has been discussed in pH 12.6, pH 10.3, and pH 8.1 environments containing 0, 0.053, and 0.2 mol/L NO2, respectively.

  20. Effects of Organic Corrosion Inhibitor and Chloride Ion Concentration on Steel Depassivation and Repassivation in Solution

    Institute of Scientific and Technical Information of China (English)

    WANG; Zixiao; YU; Lei; LIU; Zhiyong; SONG; Ning

    2015-01-01

    Effect of an organic corrosion inhibitor(OCI) named PCI-2014 added in chloride solution on the critical chloride concentration of mild steel depassivation and the critical OCI concentrations for repairing the steel in different chloride solution were investigated.The results show that the critical chloride concentration increases exponentially with raises of PCI-2014 concentration in the solution.Within a certain chloride ion concentration range,the critical PCI-2014 concentration for repairing the corroded steel is also increases exponentially with enhancement of chloride content in the solution.Atomic force microscopy images display the molecular particles of inhibitor are adsorbed on the steel surface and formed a protective layer.Analysis of X-ray photoelectron spectroscopy shows the chloride ions at the surface of steel are displaced by atoms or molecules of the inhibitor in chloride condition.

  1. Effects of Organic Corrosion Inhibitor and Chloride Ion Concentration on Steel Depassivation and Repassivation in Solution

    Institute of Scientific and Technical Information of China (English)

    WANG Zixiao; YU Lei; LIU Zhiyong; SONG Ning

    2015-01-01

    Effect of an organic corrosion inhibitor (OCI) named PCI-2014 added in chloride solution on the critical chlo-ride concentration of mild steel depassivation and the critical OCI concentrations for repairing the steel in different chlo-ride solution were investigated. The results show that the critical chloride concentration increases exponentially with raises of PCI-2014 concentration in the solution. Within a certain chloride ion concentration range, the critical PCI-2014 concentration for repairing the corroded steel is also increases exponentially with enhancement of chloride content in the solution. Atomic force microscopy images display the molecular particles of inhibitor are adsorbed on the steel surface and formed a protective layer. Analysis of X-ray photoelectron spectroscopy shows the chloride ions at the surface of steel are displaced by atoms or molecules of the inhibitor in chloride condition.

  2. A novel capsule-based selfrecovery system with a chloride ion trigger

    NARCIS (Netherlands)

    Xiong, W.; Tang, J.; Zhu, G.; Han, N.; Schlangen, E.; Dong, B.; Wang, X.; Xing, F.

    2015-01-01

    Steel is prone to corrosion induced by chloride ions, which is a serious threat to reinforced concrete structures, especially in marine environments. In this work, we report a novel capsule-based selfrecovery system that utilizes chloride ions as a trigger. These capsules, which are functionalized v

  3. Erratum to: Study on Chloride Ion Penetration Resistance of Rubberized Concrete Under Steady State Condition

    Directory of Open Access Journals (Sweden)

    Md Noor Nurazuwa

    2016-01-01

    In this paper, the effect of crumb rubber, CR as fine aggregate in the concrete to enhance concrete durability against chloride ion diffusion was studied. Chloride ion diffusion in rubberized concrete was tested by migration test under steady state condition. Concrete specimen with water-to-cement ratio of 0.50 was prepared to study the CR effectiveness in comparison with lower water-to-cement ratio. In addition, 10% silica fume, SF was added to provide denser concrete and to understand its effectiveness against chloride ion diffusion. Results showed that chloride transport characteristics were improved by the increasing amount of CR in all mixed due to the fact that CR has the ability to repel water. Meanwhile, rubberized concrete with w/c = 0.35 gave better resistance against chloride ion penetration compared to w/c = 0.50. This was much improved with combination of CR and SF.

  4. Chloride Ion Transmission Model under the Drying-wetting Cycles and Its Solution

    Institute of Scientific and Technical Information of China (English)

    HUANG Ying; WEI Jun; DONG Rongzhen; ZENG Hua

    2014-01-01

    The chloride ion transmission model considering diffusion and convection was established respectively for different zones in concrete by analyzing chloride ion transmission mechanism under the drying-wetting cycles. The finite difference method was adopted to solve the model. The equation of chloride ion transmission model in the convection and diffusion zone of concrete was discreted by the group explicit scheme with right single point (GER method) and the equation in diffusion zone was discreted by FTCS difference scheme. According to relative humidity characteristics in concrete under drying-wetting cycles, the seepage velocity equation was formulated based on Kelvin Equation and Darcy’s Law. The time-variant equations of chloride ion concentration of concrete surface and the boundary surface of the convection and diffusion zone were established. Based on the software MATLAB the numerical calculation was carried out by using the model and basic material parameters from the experiments. The calculation of chloride ion concentration distribution in concrete is in good agreement with the drying-wetting cycles experiments. It can be shown that the chloride ion transmission model and the seepage velocity equation are reasonable and practical. Studies have shown that the chloride ion transmission in concrete considering convection and diffusion under the drying-wetting cycles is the better correlation with the actual situation than that only considering the diffusion.

  5. Diffusion Decay Coefficient for Chloride Ions of Concrete Containing Mineral Admixtures

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    Jae-Im Park

    2016-01-01

    Full Text Available The diffusion coefficient for chloride ions and the diffusion decay coefficient for chloride ions are essential variables for a service life evaluation of concrete structures. They are influenced by water-binder ratio, exposure condition, curing temperature, cement type, and the type and use of mineral admixture. Mineral admixtures such as ground granulated blast furnace slag, fly ash, and silica fume have been increasingly used to improve resistance against chloride ions penetration in concrete structures built in an offshore environment. However, there is not enough measured data to identify the statistical properties of diffusion decay coefficient for chloride ions in concrete using mineral admixtures. This paper is aimed at evaluating the diffusion decay coefficient for chloride ions of concrete using ordinary Portland cement or blended cement. NT BUILD 492 method, an electrophoresis experiment, was used to measure the diffusion coefficient for chloride ions with ages. It was revealed from the test results that the diffusion decay coefficient for chloride ions was significantly influenced by W/B and the replacement ratio of mineral admixtures.

  6. Ion selective electrode for determination of chloride ion in biological materials, food products, soils and waste water.

    Science.gov (United States)

    Sekerka, I; Lechner, J F

    1978-11-01

    The chloride ion selective electrode is used for a rapid, simple, and reliable determination of chloride ion in biological materials (blood serum, urine, fish, and plant tissues), food products (milk, beef extract, nutrient broth and orange, tomato, and grapefruit juices), soils, and waste water (industrial and municipal). The method consists of treating the samples with perchloric acid (pH 1) and potassium peroxydisulfate and determining the chloride content either by a calibration curve or by known addition or analyte addition, using the chloride ion selective electrode. Such sample treatment eliminates most of the interferences occurring in the samples, including iodide, complexing and reducing compounds, and macromolecular and surface-active species. The method is suitable for a wide range of chloride concentration, e.g., 5010 ppm Cl- in nutrient broth and 4890 ppm in beef extract and as low as 12 and 80 ppm in soil extracts.

  7. The Role of Chloride Ions during the Formation of Akaganéite Revisited

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    Johanna Scheck

    2015-11-01

    Full Text Available Iron(III hydrolysis in the presence of chloride ions yields akaganéite, an iron oxyhydroxide mineral with a tunnel structure stabilized by the inclusion of chloride. Yet, the interactions of this anion with the iron oxyhydroxide precursors occurring during the hydrolysis process, as well as its mechanistic role during the formation of a solid phase are debated. Using a potentiometric titration assay in combination with a chloride ion-selective electrode, we have monitored the binding of chloride ions to nascent iron oxyhydroxides. Our results are consistent with earlier studies reporting that chloride ions bind to early occurring iron complexes. In addition, the data suggests that they are displaced with the onset of oxolation. Chloride ions in the akaganéite structure must be considered as remnants from the early stages of precipitation, as they do not influence the basic mechanism, or the kinetics of the hydrolysis reactions. The structure-directing role of chloride is based upon the early stages of the reaction. The presence of chloride in the tunnel-structure of akagenéite is due to a relatively strong binding to the earliest iron oxyhydroxide precursors, whereas it plays a rather passive role during the later stages of precipitation.

  8. Method of effective evaluation for examination of chloride ion in concrete

    Institute of Scientific and Technical Information of China (English)

    SUNG Wen-pei; CHEN Kuen-suan; LIN Hsue-chun

    2005-01-01

    The chloride ion contained in reinforced concrete seriously corrodes the steel surface and damages concrete, resulting in inferior reinforced concrete that strength seriously compromises the entire structure's safety. Consequently, the examination of chloride ions contained in reinforced concrete becomes an important part of a complete quality control procedure. To effectively check the concentration of chloride ions in concrete, the evaluation process should be accurate and precise. Laboratory data obtained using existing evaluation methods for the examination of chloride ion are not sufficiently objective to yield reliable results with accuracy and consistency for each sample. An evaluation algorithm with capability to define indices of precision degree (Ep)and accuracy degree (Ea) is presented in this paper. The authors established a statistically reliable index of unbiased estimators and equations to critically examine the laboratory methods' precision, accuracy degrees and application value for measuring chlorine ion concentration in reinforced concrete.

  9. Chloride Ion Transport in Fly Ash Mortar under Action of Fatigue Loading

    Institute of Scientific and Technical Information of China (English)

    WANG Caihui; SUN Wei; JIANG Jinyang

    2012-01-01

    In order to study the chloride ion transport performance in fly ash addition mortar,a new method,in which the fatigue loading and chloride diffusion are undertaken simultaneously,was developed.This method realizes coupling the fatigue damage process and the process of chloride transporting of fly ash mortar.The transport performance of chloride in fly ash mortar specimens was studied under different stress levels.Moreover,the effect of fly ash content on transport performance of chloride ion in mortar was investigated.AE (Acoustic Emission) and SEM were used to acquire the damage distribution of mortar specimens under action of fatigue load.The results show that the diffusion coefficient of chloride in mortar specimens increases with stress level of fatigue loading.The addition of fly ash can mitigate the penetration of chloride ion.The results of microcrack 3D location acquired by AE,accompanied with crack characterizing from SEM,indicate that the damage degree of mortar specimen increases with stress level of fatigue loading.Furthermore,higher damage degree of mortar leads to more the chloride ion content in the sample.

  10. Facile Preparation of Chloride-Conducting Membranes: First Step towards a Room-Temperature Solid-State Chloride-Ion Battery.

    Science.gov (United States)

    Gschwind, Fabienne; Steinle, Dominik; Sandbeck, Daniel; Schmidt, Celine; von Hauff, Elizabeth

    2016-12-01

    Three types of chloride-conducting membranes based on polyvinyl chloride, commercial gelatin, and polyvinyldifluoride-hexafluoropolymer are introduced in this report. The polymers are mixed with chloride-containing salts, such as tetrabutylammonium chloride, and cast to form membranes. We studied the structural properties, thermal stability, and electrochemical response of the membranes to understand chloride migration and transport. Finally, the membranes are tested in a prototype solid-state chloride-ion battery setup. The feasibility of the membranes for their potential use in anion batteries is discussed.

  11. The development of chloride ion selective polypyrrole thin film on a layer-by-layer carbon nanotube working electrode

    Science.gov (United States)

    Liu, Yang; Lynch, Jerome

    2011-04-01

    A chloride ion selective thin film sensor is proposed for measuring chloride ion concentration, which is an environmental parameter correlated to corrosion. In this work, electrochemical polymerization of Polypyrrole (PPy) doped with chloride ions was achieved on the top of a carbon nanotube (CNT) thin film as a working electrode in an electrochemical cell. The underlying CNT layer conjugated with doped PPy thin film can form a multifunctional "selfsensing" material platform for chloride ion detection in a concrete environment. The paper presents the first type of work using CNT and PPy as hybrid materials for chloride ion sensing. Electrochemical polymerization of PPy results in oxidation that yields an average of one positive charge distributed over four pyrrole units. This positive charge is compensated by negatively-charged chloride ions in the supporting electrolyte. In effect, the chloride ion-doped PPy has become molecularly imprinted with chloride ions thereby providing it with some degree of perm-selectivity for chloride ions. The detection limit of the fabricated chloride ion-doped PPy thin film can reach 10-8 M and selectivity coefficients are comparable to those in the literature. The reported work aims to lay a strong foundation for detecting chloride ion concentrations in the concrete environment.

  12. The Effect of Chloride Ions on the Activity of Cerussite Surfaces

    Directory of Open Access Journals (Sweden)

    Qicheng Feng

    2016-09-01

    Full Text Available Chloride ions were found to potentially increase activity of cerussite surfaces. Dissolution experiments, zeta potential measurements, X-ray photoelectron spectroscopy (XPS studies, and density functional theory (DFT computation were conducted in this study. Dissolution experiments showed that the lead ion concentrations in the NaCl solution system were lower than those in the deionized water system and that the lead ion concentrations in NaCl + Na2S aqueous systems decreased by approximately one order of magnitude compared with that in the Na2S system alone. Results of zeta potential measurements revealed that the pretreatment with chloride ions of cerussite caused a more positive zeta potential than that without chloride ions. XPS analysis results indicated that the number of lead ions on the mineral surface increased after cerussite was treated with chloride ions. Results of DFT computation implied that the number of lead atoms on the mineral surface increased and that the activity improved after PbCl+ was adsorbed onto the cerussite surface. The contribution of chloride ions to the activity on the mineral surface is attributed to the increase in the number of active sites and enhancement in the activity of these sites, resulting in improved sulfidization and flotation performance.

  13. Removal of sodium and chloride ions from aqueous solutions using fique fibers (Furcraea spp.).

    Science.gov (United States)

    Agudelo, Nikolay; Hinestroza, Juan P; Husserl, Johana

    2016-01-01

    Fique fibers obtained from the leaves of Furcraea spp., a highly abundant plant in the mountains of South America, may offer an alternative as biosorbents in desalination processes as they exhibit high removal capacities (13.26 meq/g for chloride ions and 15.52 meq/g for sodium ions) up to four times higher than exchange capacities commonly observed in synthetic resins. The ion removal capacity of the fibers was also found to be a function of the pH of the solution with the maximum removal of ions obtained at pH 8. Unlike most commercial ion exchange resins, our results suggest that fique fibers allow simultaneous removal of chloride and sodium ions.

  14. Radiotracer studies on calcium ion-selective electrode membranes based on poly(vinyl chloride) matrices.

    Science.gov (United States)

    Craggs, A; Moody, G J; Thomas, J D; Willcox, A

    Radiotracer studies with (45)Ca and (36)Cl demonstrate that PVC matrix membranes containing Orion 92-20-02 liquid calcium ion-exchanger are permselective to counter-cations. Diffusion coefficients are quoted for the migration of (45)Ca between pairs of calcium solutions and are discussed in terms of solution concentration, membrane thickness and concentration level of sensor in the membrane. Migration of calcium ions from calcium chloride solution to a Group (II) metal chloride solution through a PVC membrane containing calcium liquid ion-exchanger is discussed in terms of solvent extraction and electrode selectivity coefficient parameters. Thus, magnesium, strontium and barium ions appear to inhibit migration through the membrane by their low affinity for the membrane liquid ion-exchanger sites, while the inhibition by beryllium ions is attributed to site blockage by the strong affinity of dialkylphosphate sites for beryllium.

  15. Synthetic ion transporters can induce apoptosis by facilitating chloride anion transport into cells.

    Science.gov (United States)

    Ko, Sung-Kyun; Kim, Sung Kuk; Share, Andrew; Lynch, Vincent M; Park, Jinhong; Namkung, Wan; Van Rossom, Wim; Busschaert, Nathalie; Gale, Philip A; Sessler, Jonathan L; Shin, Injae

    2014-10-01

    Anion transporters based on small molecules have received attention as therapeutic agents because of their potential to disrupt cellular ion homeostasis. However, a direct correlation between a change in cellular chloride anion concentration and cytotoxicity has not been established for synthetic ion carriers. Here we show that two pyridine diamide-strapped calix[4]pyrroles induce coupled chloride anion and sodium cation transport in both liposomal models and cells, and promote cell death by increasing intracellular chloride and sodium ion concentrations. Removing either ion from the extracellular media or blocking natural sodium channels with amiloride prevents this effect. Cell experiments show that the ion transporters induce the sodium chloride influx, which leads to an increased concentration of reactive oxygen species, release of cytochrome c from the mitochondria and apoptosis via caspase activation. However, they do not activate the caspase-independent apoptotic pathway associated with the apoptosis-inducing factor. Ion transporters, therefore, represent an attractive approach for regulating cellular processes that are normally controlled tightly by homeostasis.

  16. Sulfate radical-based degradation of polychlorinated biphenyls: Effects of chloride ion and reaction kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Fang, Guo-Dong [Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100049 (China); Dionysiou, Dionysios D. [Environmental Engineering and Science Program, University of Cincinnati, Cincinnati, OH 45221-0071 (United States); Wang, Yu [Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100049 (China); Al-Abed, Souhail R. [National Risk Management Research Laboratory, U.S. Environmental Protection Agency, 26 West Martin Luther King Drive, Cincinnati, OH 45268 (United States); Zhou, Dong-Mei, E-mail: dmzhou@issas.ac.cn [Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008 (China)

    2012-08-15

    Highlights: Black-Right-Pointing-Pointer A kinetic model was used to predict the radical species and their distributions. Black-Right-Pointing-Pointer The generated radical species were identified by EPR. Black-Right-Pointing-Pointer The second-order rate constants of sulfate radical with PCBs were determined. - Abstract: Advanced oxidation processes (AOPs) based on sulfate radical (SO{sub 4}{center_dot}{sup -}) have been recently used for soil and groundwater remediation. The presence of chloride ion in natural or wastewater decreases the reactivity of sulfate radical system, but explanations for this behavior were inconsistent, and the mechanisms are poorly understood. Therefore, in this paper we investigated the effect of chloride ion on the degradation of 2,4,4 Prime -CB (PCB28) and biphenyl (BP) by persulfate, based on the produced SO{sub 4}{center_dot}{sup -}. The results showed that the presence of chloride ion greatly inhibited the transformation of PCB28 and BP. Transformation intermediates of BP were monitored, suggesting that the chloride ion can react with SO{sub 4}{center_dot}{sup -} to produce chlorine radical, which reacts with BP to generate chlorinated compounds. To better understand the underlying mechanisms of these processes, a kinetic model was developed for predicting the effect of chloride ion on the types of radical species and their distributions. The results showed that chloride ion could influence the selectivity of radical species and their distribution, and increase the concentration of the sum of radical species. In addition, the second-order rate constants of sulfate radical with PCBs were determined, and quantum-chemical descriptors were introduced to predict the rate constants of other PCBs based on our experimental data.

  17. Halogen-bonding for visual chloride ion sensing: a case study using supramolecular poly(aryl ether) dendritic organogel systems.

    Science.gov (United States)

    Liu, Zhi-Xiong; Sun, Yihua; Feng, Yu; Chen, Hui; He, Yan-Mei; Fan, Qing-Hua

    2016-02-07

    A convenient and straightforward method for the visual recognition of chloride ion has been established through a chloride-responsive dendritic organogel. The specificity was largely attributed to the higher binding affinity of the dendritic gelator for chloride compared with other anions through halogen bonding interactions.

  18. Concrete Durability. Influence of chloride ions concentrations in mixing water and dissolution

    Directory of Open Access Journals (Sweden)

    López Villarino, Begoña

    1995-03-01

    Full Text Available The most aggressive situation which is responsible for most of the cases of steel reinforcement corrosion in concrete, takes place when chlorides are present in the environment. These chlorides destroy the passivating film of steel and promote the denominated pitting corrosion. In order to study the demonstrated corrosive action of chloride ions on concrete structures, a number of experiments have been designed, to quantify the effect of different amounts of this ion in concrete. Several mixes have been prepared with portland cement type II-C-35 to which it has been added, as an additive in mixing water, NaCl in increasing concentrations. The samples obtained were submerged in different dissolutions of NaCl. From the results obtained it is clear that the chloride content in mixing water does not affect the flux of calcium ions; however, its influence on the flux of chloride ions is significant. Likewise, it is confirmed that the existence of chloride ions in dissolution influences the migration of calcium and chloride ions.

    La situación más agresiva, y la responsable del mayor número de casos de corrosión de armaduras en el hormigón, se da cuando en el ambiente hay presencia de cloruros, pues éstos destruyen de forma puntual la capa pasivante del acero, lo que provoca la denominada corrosión por picaduras. Con objeto de estudiar la demostrada acción perniciosa de los cloruros sobre las estructuras de hormigón, se ha diseñado un conjunto de ensayos con el fin de cuantificar el efecto de las distintas cantidades de este ion en la masa de hormigón. Se han realizado diversas amasadas con cemento tipo II-C-35 a las que se añadió, como aditivo en el agua de amasado, NaCl en concentraciones crecientes. Las probetas obtenidas se sumergieron en disoluciones de NaCl de distintas concentraciones. De los resultados obtenidos se deduce que la presencia de cloruros en el agua de amasado no afecta al flujo de iones cálcicos, mientras

  19. Chloride ion-aided self-assembly of pseudoclathrochelate metal tris-pyrazoloximates.

    Science.gov (United States)

    Varzatskii, Oleg A; Penkova, Larysa V; Kats, Svitlana V; Dolganov, Alexander V; Vologzhanina, Anna V; Pavlov, Alexander A; Novikov, Valentin V; Bogomyakov, Artem S; Nemykin, Victor N; Voloshin, Yan Z

    2014-03-17

    Chloride ion-aided one-pot template self-assembly of a mixed pyrazoloxime ligand with phenylboronic acid on a corresponding metal(II) ion as a matrix afforded the first boron-capped zinc, cobalt, iron, and manganese pseudoclathrochelate tris-pyrazoloximates. The presence of a pseudocross-linking hydrogen-bonded chloride ion is critical for their formation, as the same chloride-capped complexes were isolated even in the presence of large excesses of bromide and iodide ions. As revealed by X-ray diffraction, all complexes are capped with a chloride ion via three N-H···Cl hydrogen bonds that stabilize their pseudomacrobicyclic frameworks. The MN6 coordination polyhedra possess a distorted trigonal prismatic geometry, with the distortion angles φ between their nonequivalent N3 bases of approximately 0°. Temperature dependences of the effective magnetic moment for the paramagnetic complexes showed the encapsulated metal(II) ions to be in a high-spin state in the temperature range of 2-300 K. In the case of the iron(II) pseudoclathrochelate, density functional theory (DFT) and time-dependent DFT calculations were used to assess its spin state as well as the (57)Fe Mössbauer and UV-vis-NIR parameters. Cyclic voltammetry studies performed for these pseudomacrobicyclic complexes showed them to undergo irreversible or quasi-reversible metal-localized oxidations and reductions. As no changes are observed in the presence of a substantial excess of bromide ion, no anion-exchange reaction occurs, and thus the pseudoclathrochelates have a high affinity toward chloride anions in solution.

  20. Studies on Ion-molecule Reaction of Disubstituted Benzene with IonSystem of Acetyl Chloride in Gas Phase

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The ion-molecule reactions of disubstituted benzenes with the ion system of acetyl chloride under the chemical ionization condition were examined and the fragmentation reactions of the adduct ions formed by the ion-molecule reactions were studied by using collision-induced dissocia tion technique. It was found that the electron-releasing groups favored the adduct reactions and the electron-withdrawing groups did not. The position and properties of substituting groups had an effect on the relative abundance of the adduct ions. The fragmentation reaction of the adduct ions formed by ortho-benzene diamine with the acetyl ion was similar to the reductive alkylation reaction of amine in condensed phase.

  1. Lactobacillus casei reduces susceptibility to type 2 diabetes via microbiota-mediated body chloride ion influx.

    Science.gov (United States)

    Zhang, Yong; Guo, Xiao; Guo, Jianlin; He, Qiuwen; Li, He; Song, Yuqin; Zhang, Heping

    2014-07-18

    Gut microbiota mediated low-grade inflammation is involved in the onset of type 2 diabetes (T2DM). In this study, we used a high fat sucrose (HFS) diet-induced pre-insulin resistance and a low dose-STZ HFS rat models to study the effect and mechanism of Lactobacillus casei Zhang in protecting against T2DM onset. Hyperglycemia was favorably suppressed by L. casei Zhang treatment. Moreover, the hyperglycemia was connected with type 1 immune response, high plasma bile acids and urine chloride ion loss. This chloride ion loss was significantly prevented by L. casei via upregulating of chloride ion-dependent genes (ClC1-7, GlyRα1, SLC26A3, SLC26A6, GABAAα1, Bestrophin-3 and CFTR). A shift in the caecal microflora, particularly the reduction of bile acid 7α-dehydroxylating bacteria, and fecal bile acid profiles also occurred. These change coincided with organ chloride influx. Thus, we postulate that the prevention of T2DM onset by L. casei Zhang may be via a microbiota-based bile acid-chloride exchange mechanism.

  2. Cellular Automata-based Chloride Ion Diffusion Simulation of Concrete Bridges under Multi-factor Coupling Actions

    Institute of Scientific and Technical Information of China (English)

    ZHU Jinsong; HE Likun

    2012-01-01

    Abstract In order to accurately simulate the diffusion of chloride ion in the existing concrete bridge and acquire the precise chloride ion concentration at given time,a cellular automata (CA)-based model is proposed.The process of chloride ion diffusion is analyzed by the CA-based method and a nonlinear solution of the Fick's second law is obtained.Considering the impact of various factors such as stress states,temporal and spatial variability of diffusion parameters and water-cement ratio on the process of chloride ion diffusion,the model of chloride ion diffusion under multi-factor coupling actions is presented.A chloride ion penetrating experiment reported in the literature is used to prove the effectiveness and reasonability of the present method,and a T-type beam is taken as an illustrative example to analyze the process of chloride ion diffusion in practical application.The results indicate that CA-based method can simulate the diffusion of chloride ion in the concrete structures with acceptable precision.

  3. Ion Transport and Microstructure of Sandwich Cementitious Materials Exposed to Chloride Environment

    Institute of Scientific and Technical Information of China (English)

    WANG Xingang; WANG Kai; WANG Rui; XIE Tao; HUANG Jie

    2015-01-01

    Ion transport of sandwich cementitious materials (SCM) exposed to chloride environment was investigated by accelerated diffusion method and natural diffusion method. Pore structure and micromorphology of SCM were investigated by MIP and SEM-EDS. In comparison with the monolayer structural high performance concrete (HPC), conductive charge for 6 hours, chloride diffusion coefficient, and apparent chloride diffusion coefifcient of SCM were decreased by 30%-40%, two orders of magnitude and 40%-50%, respectively. Pore structure of ultra low ion permeability cementitious materials (ULIPCM) prepared for the facesheet is superior to that of HPC prepared for the core. As for porosity, the most probable pore radius, the content of pores with radius 50 nm and the surface area of pores, the order is ULIPCM

  4. Dynamic fluorescence quenching of quinine sulfate dication by chloride ion in ionic and neutral micellar environments

    Science.gov (United States)

    Joshi, Sunita; Varma Y, Tej Varma; Pant, Debi D.

    2014-04-01

    Fluorescence quenching of Quinine sulfate dication (QSD) by chloride-ion (Cl-) in micellar environments of anionic, sodium dodecyl sulfate (SDS), cationic, cetyltrimethylammonium bromide (CTAB) and neutral, triton X-100 (TX-100) in aqueous phase has been investigated by time-resolved and steady- state fluorescence measurements. The quenching follows linear Stern-Volmer relation in micellar solutions and is dynamic in nature.

  5. Electrochemical Behavior of Nano-grained Pure Copper in Dilute Alkaline Solution with Chloride Ion Trace

    Science.gov (United States)

    Fattah-Alhosseini, Arash; Imantalab, Omid; Attarzadeh, Farid Reza

    2016-10-01

    Effect of nano-grained structure on the interface behavior of pure copper in 0.01M KOH solution with chloride ion trace is investigated by various electrochemical techniques. Nano-grained structure was achieved by accumulative roll bonding (ARB) technique. Before any electrochemical measurements, microstructure was evaluated by means of optical microscopy and transmission electron microscopy (TEM). TEM observations showed that nano-grains (with an average size of below 100 nm) appeared after eight passes of ARB. Polarization curves revealed that increasing chloride ion concentration leads to a decrease in the corrosion and pitting potentials of both annealed and nano-grained pure copper samples. Electrochemical impedance spectroscopy revealed that chloride ion trace lowers passive film resistance and charge-transfer resistance in both annealed and nano-grained samples. Mott-Schottky analysis showed that the surface films formed on annealed and nano-grained samples in KOH solution with and without NaCl addition are of p-type semiconducting behavior. Moreover, this analysis showed that the acceptor density increases by increasing chloride ion concentration.

  6. Effect of temperature, chloride ions and sulfide ions on the electrochemical properties of 316L stainless steel in simulated cooling water

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The influence of temperature, chloride ions and sulfide ions on the anticorrosion behavior of 316L stainless steel in simulated cooling water was studied by electrochemical impedance spectroscopy and anodic polarization curves. The results show that the film resistance increases with the solution temperature but decreases after 8 days' immersion, which indicates that the film formed at higher temperature has inferior anticorrosion behavior; Chloride ions and sulfide ions have remarkable effects on the elect...

  7. Stability constants of the Europium complexes with the chloride ions; Constantes de estabilidad de los complejos del europio con los iones cloruro

    Energy Technology Data Exchange (ETDEWEB)

    Jimenez R, M.; Solache R, M.; Rojas H, A. [Instituto Nacional de Investigaciones Nucleares, Departamento de Quimica, A.P. 18-1027, C.P. 11801 Mexico D.F. (Mexico)

    2000-07-01

    The stability constants of lanthanides complexes with chloride ions which were determined at the same ionic force but in different media, are significantly different. It does not exist a systematic study over these stability constants. The purpose of this work is to determine the stability constants of the europium complexes with chloride ions at 303 K, by the solvents extraction method. (Author)

  8. Durability of reinforced adobe exposed to chloride ions

    Directory of Open Access Journals (Sweden)

    Giménez, A.

    2006-12-01

    Full Text Available One of the primary shortcomings of adobe, a dried mudblock stabilized with sisal hemp and cement widely used across all of Latin America, is its dimensional instability when exposed to water or aggressive environments. The present paper evaluates the electrochemical performance of reinforced adobe block after 1,000 days of exposure to a simulated marine environment. The specimens used were adobe blocks internally reinforced with 3/8-inch steel bars. The specimens were watered every two weeks: one group with potable water to simulate a natural urban environment and the other with a 3% sodium chloride solution to simulate a marine environment.Chloride penetration in powder extracted from the specimens was determined using the Mohr method. Electrochemical measurements included Gecor 6 electric potential(Eº and corrosion intensity (icorr readings. The final conclusion drawn from an analysis of the results was that in all cases the amount of free chlorides present sufficed to depassivate reinforcing steel and that the system component providing the most effective protection was the rough casting mortar. Consequently, this type of adobe mixes is not recommended for use in marine or industrial environments.La tierra-cemento-sisal es un material cuyo uso se encuentra muy difundido en toda Latinoamérica, entre sus principales limitaciones está la inestabilidad volumétrica ante el agua y ambientes agresivos. Por tal motivo, en este trabajo se evaluó el comportamiento electroquímico de bloques de tierra-cemento-sisal armado expuestos durante 1.000 días a un ambiente marino simulado. Las probetas utilizadas fueron bloques de tierra-cemento-sisal incorporándole internamente barras de acero de 3/8 de pulg. Las probetas se sometieron a un rociado quincenal: las de ambiente natural urbano con agua potable y las de ambiente marino simulado con una solución al 3% de cloruro de sodio. La penetración de cloruros se determinó extrayendo polvillo y

  9. Exhaustive removal of chloride ions from water with the aid of a bismuth-based metallic sorbent

    Energy Technology Data Exchange (ETDEWEB)

    Moskvin, L.N.; Ushenko, V.G.

    1988-04-20

    The authors discuss the sorption properties of sorbents based on metallic bismuth, in relation to a solution of the problem of exhaustive removal of chloride ions from water. Metallic sorbents with bismuth contents of 10 mass % on polytetrafluoroethylene were used. The sorption properties of sorbents based on metallic bismuth and on Bi/sub 2/O/sub 3/ were studied under dynamic conditions. Their results show that bismuth-based metal sorbents and sorbents based on bismuth oxide can be used as inorganic anion-exchangers. In order to demonstrate the possibility of selective separation of chloride ions from solutions they determined the dynamic exchange capacity for chloride ions at various nitrate-ion concentrations. The use of the proposed sorbents based on metallic bismuth for exhaustive purification of water lowers the chloride-ion concentration in the water sharply in comparison with the level achieved by ion-exchange purification with the aid of organic anion-exchangers.

  10. Strontium Ions Substitution in Brushite Crystals: The Role of Strontium Chloride

    Directory of Open Access Journals (Sweden)

    Enrique López Cabarcos

    2011-05-01

    Full Text Available The incorporation of strontium chloride to brushite cement was successful to introduce strontium ions within the lattice of brushite crystals. The effect of strontium ions on brushite cement properties was concentration dependent; such that, the addition of 5% and 10% (w/w SrCl2 significantly increased the cement FST and the addition of 10% SrCl2 decreased the cement tensile strength. Further, cement weight loss was shown to be increased by cement modification with SrCl2. The combination of ionic substitution and the degradability of brushite cements would constitute a system for the local delivery of strontium ions in the treatment of osteoporosis.

  11. Strontium ions substitution in brushite crystals: the role of strontium chloride.

    Science.gov (United States)

    Alkhraisat, Mohammad H; Rueda, Carmen; López Cabarcos, Enrique

    2011-05-31

    The incorporation of strontium chloride to brushite cement was successful to introduce strontium ions within the lattice of brushite crystals. The effect of strontium ions on brushite cement properties was concentration dependent; such that, the addition of 5% and 10% (w/w) SrCl2 significantly increased the cement FST and the addition of 10% SrCl2 decreased the cement tensile strength. Further, cement weight loss was shown to be increased by cement modification with SrCl2. The combination of ionic substitution and the degradability of brushite cements would constitute a system for the local delivery of strontium ions in the treatment of osteoporosis.

  12. Method for the determination of dissolved chloride, nitrate, and sulfate in natural water using ion chromatography

    Science.gov (United States)

    Brinton, Terry I.; Antweiler, Ronald C.; Taylor, Howard E.

    1996-01-01

    Ion chromatography was used for the determination of dissolved chloride, nitrate and sulfate in natural water where concentrations ranged from a detection limit of 0.02 milligrams per liter to 80 milligrams per liter for chloride, to 18 milligrams per liter for nitrate, and to 280 milligrams per liter for sulfate. Specific conductance was the mode of detection used. Three analytical sample size loops of 11, 61, and 250 microliters, were used to include the analytical ranges described. U.S. Geological Survey Standard Reference Water Samples were analyzed to test the precision and accuracy of the analyses.

  13. Mechanism of radiosensitizing effect of chloride ion on E. coli

    Energy Technology Data Exchange (ETDEWEB)

    Shih-Chen, S.J.; Kitayama, S.; Matsuyama, A.; Arai, S.; Masuda, T.

    1986-05-01

    Cells of E. coli capable of repairing DNA damage are sensitized to radiation in the presence of NaCl. However, the enhanced radiolethality was suppressed by the addition of compounds such as an amino acid to the irradiation buffer. The protective efficiencies of these compounds depend on their reactivities with Cl/sub 2/ion radical or OH radical. ATP synthesis in the cells irradiated in the presence of NaCl was severely inhibited depending on the dose of irradiation. This reduced rate of ATP synthesis can account for the inhibition of protein, RNA and DNA synthesis in the irradiated cells with NaCl.

  14. Strontium Ions Substitution in Brushite Crystals: The Role of Strontium Chloride

    OpenAIRE

    2011-01-01

    The incorporation of strontium chloride to brushite cement was successful to introduce strontium ions within the lattice of brushite crystals. The effect of strontium ions on brushite cement properties was concentration dependent; such that, the addition of 5% and 10% (w/w) SrCl2 significantly increased the cement FST and the addition of 10% SrCl2 decreased the cement tensile strength. Further, cement weight loss was shown to be increased by cement modification with SrCl2. The combination of ...

  15. A Microfluidic Long-Period Fiber Grating Sensor Platform for Chloride Ion Concentration Measurement

    Directory of Open Access Journals (Sweden)

    Jian-Neng Wang

    2011-09-01

    Full Text Available Optical fiber sensors based on waveguide technology are promising and attractive in chemical, biotechnological, agronomy, and civil engineering applications. A microfluidic system equipped with a long-period fiber grating (LPFG capable of measuring chloride ion concentrations of several sample materials is presented. The LPFG-based microfluidic platform was shown to be effective in sensing very small quantities of samples and its transmitted light signal could easily be used as a measurand. The investigated sample materials included reverse osmosis (RO water, tap water, dilute aqueous sample of sea sand soaked in RO water, aqueous sample of sea sand soaked in RO water, dilute seawater, and seawater. By employing additionally a chloride ion-selective electrode sensor for the calibration of chloride-ion concentration, a useful correlation (R2 = 0.975 was found between the separately-measured chloride concentration and the light intensity transmitted through the LPFG at a wavelength of 1,550 nm. Experimental results show that the sensitivity of the LPFG sensor by light intensity interrogation was determined to be 5.0 × 10−6 mW/mg/L for chloride ion concentrations below 2,400 mg/L. The results obtained from the analysis of data variations in time-series measurements for all sample materials show that standard deviations of output power were relatively small and found in the range of 7.413 × 10−5–2.769 × 10−3 mW. In addition, a fairly small coefficients of variations were also obtained, which were in the range of 0.03%–1.29% and decreased with the decrease of chloride ion concentrations of sample materials. Moreover, the analysis of stability performance of the LPFG sensor indicated that the random walk coefficient decreased with the increase of the chloride ion concentration, illustrating that measurement stability using the microfluidic platform was capable of measuring transmitted optical power with accuracy in the range of −0

  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. Photochemical oxidation of chloride ion by ozone in acid aqueous solution.

    Science.gov (United States)

    Levanov, Alexander V; Isaykina, Oksana Ya; Amirova, Nazrin K; Antipenko, Ewald E; Lunin, Valerii V

    2015-11-01

    The experimental investigation of chloride ion oxidation under the action of ozone and ultraviolet radiation with wavelength 254 nm in the bulk of acid aqueous solution at pH 0-2 has been performed. Processes of chloride oxidation in these conditions are the same as the chemical reactions in the system O3 - OH - Cl(-)(aq). Despite its importance in the environment and for ozone-based water treatment, this reaction system has not been previously investigated in the bulk solution. The end products are chlorate ion ClO3(-) and molecular chlorine Cl2. The ions of trivalent iron have been shown to be catalysts of Cl(-) oxidation. The dependencies of the products formation rates on the concentrations of O3 and H(+) have been studied. The chemical mechanism of Cl(-) oxidation and Cl2 emission and ClO3(-) formation has been proposed. According to the mechanism, the dominant primary process of chloride oxidation represents the complex interaction with hydroxyl radical OH with the formation of Cl2(-) anion-radical intermediate. OH radical is generated on ozone photolysis in aqueous solution. The key subsequent processes are the reactions Cl2(-) + O3 → ClO + O2 + Cl(-) and ClO + H2O2 → HOCl + HO2. Until the present time, they have not been taken into consideration on mechanistic description and modelling of Cl(-) oxidation. The final products are formed via the reactions 2ClO → Cl2O2, Cl2O2 + H2O → 2H(+) + Cl(-) + ClO3(-) and HOCl + H(+) + Cl(-) ⇄ H2O + Cl2. Some portion of chloride is oxidized directly by O3 molecule with the formation of molecular chlorine in the end.

  18. Changes in acceleration rate of chloride ions depending on climatic conditions. Influence of rain

    Directory of Open Access Journals (Sweden)

    Corvo, F.

    2003-12-01

    Full Text Available Mild steel, copper and aluminium samples were exposed outdoors in two atmospheric test stations located in Havana, Cuba and Medellín, Colombia. Two parallel group of samples were formed, one for each station. They were submitted to accelerated outdoor test by intermittent spraying of a salt solution (SCAB test according to ISO 11474:98, receiving also the influence of the open atmosphere. The acceleration of corrosion rate of the three metals caused by the presence of chloride ions in both stations was determined. As expected, steel shows the higher corrosion rate and acceleration by chlorides, particularly at Cuban corrosion station. A remarkable difference in the acceleration rate of chloride ions for mild steel and copper between Cuban and Colombian acceleration rate of chloride ions of steel and copper. Steel corrosion products were analyzed by Mössbauer Spectroscopy. Water absorption was also studied. The presence of magnetite, goethite and other Iron compounds was determined.

    Probetas de acero de bajo carbono, cobre y aluminio se expusieron a la intemperie en dos estaciones de ensayo localizadas en la Habana, Cuba y Medellín, Colombia. Se formaron dos grupos paralelos de probetas, tomándose uno para cada estación. Ambos grupos fueron sometidos a ensayos acelerados a la intemperie mediante la aplicación de una niebla salina (SCAB TEST de acuerdo a la Norma ISO 11474:98, recibiendo también la influencia de la atmósfera abierta. Se determinó la aceleración de la velocidad de corrosión de los tres metales causada por la presencia de iones cloruro en ambas estaciones. Como era de esperar, el acero muestra la mayor velocidad de corrosión y aceleración por los iones cloruro, particularmente en la estación de ensayos cubana. Se determinó una notable diferencia en la velocidad de aceleración provocada por los cloruros para el acero de bajo carbono y el cobre entre las estaciones cubana y colombiana. La influencia de la lluvia

  19. Polarizabilities and Shielding Factors of Ions in Cesium Halide Crystals with the Cesium Chloride Structure

    Science.gov (United States)

    Mahbubar, Rahman; Michihiro, Yoshitaka; Nakamura, Koichi; Kanashiro, Tatsuo

    2001-08-01

    The calculated results of the polarizabilities and the quadrupole shielding factor of the ions in cesium halide crystals with the cesium chloride structure are presented. The calculation is done on the basis of the self-consistent field local density approximation and the modified Sternheimer equation. The crystalline potential is treated by the spherical solid model. The size effect is seen in the values of the polarizabilities and the quadrupole shielding factor. The values of the polarizabilities and the quadrupole shielding factor of cesium ion show only slight change in different crystals. The values of chlorine ion show significant reduction and the amount of the reduction is different in the different crystals. The effect of the crystalline environment on the electron states is discussed.

  20. Effect of temperature, chloride ions and sulfide ions on the electrochemical properties of 316L stainless steel in simulated cooling water

    Institute of Scientific and Technical Information of China (English)

    Li Jinbo; Zhai Wen; Zheng Maosheng; Zhu Jiewu

    2008-01-01

    The influence of temperature, chloride ions and sulfide ions on the anticorrosion behavior of 316L stainless steel in simulated cooling water was studied by electrochemical impedance spectroscopy and anodic polarization curves. The results show that the film resistance increases with the solution temperature but decreases after 8 days' immersion, which indicates that the film formed at higher temperature has inferior anticorrosion behavior; Chloride ions and sulfide ions have remarkable effects on the electrochemical property of 316L stainless steel in simulated cooling water and the pitting potential declines with the concentration of chloride ions; the passivation current has no obvious effect; the rise of the concentration of sulfide ions obviously increases the passivation current, but the pitting potential changes little, which indicates that the two types of ions may have different effects on destructing passive film of stainless steel. The critical concentration of chloride ions causing anodic potential curve's change in simulated cooling water is 250 mg/L for 316 L stainless. The effect of sulfide ions on the corrosion resistance behavior of stainless steel is increasing the passivation current density Ip. The addition of 6mg/L sulfide ions to the solution makes Ip of 316 L increase by 0.5 times.

  1. Potential energy, force distribution and oscillatory motion of chloride ion inside electrically charged carbon nanotubes

    Science.gov (United States)

    Sadeghi, F.; Ansari, R.; Darvizeh, M.

    2016-06-01

    In this research, a continuum-based model is presented to explore potential energy, force distribution and oscillatory motion of ions, and in particular chloride ion, inside carbon nanotubes (CNTs) decorated by functional groups at two ends. To perform this, van der Waals (vdW) interactions between ion and nanotube are modeled by the 6-12 Lennard-Jones (LJ) potential, whereas the electrostatic interactions between ion and functional groups are modeled by the Coulomb potential and the total interactions are analytically derived by summing the vdW and electrostatic interactions. Making the assumption that carbon atoms and charge of functional groups are all uniformly distributed over the nanotube surface and the two ends of nanotube, respectively, a continuum approach is utilized to evaluate the related interactions. Based on the actual force distribution, the equation of motion is also solved numerically to arrive at the time history of displacement and velocity of inner core. With respect to the proposed formulations, comprehensive studies on the variations of potential energy and force distribution are carried out by varying functional group charge and nanotube length. Moreover, the effects of these parameters together with initial conditions on the oscillatory behavior of system are studied and discussed in detail. It is found out that chloride ion escapes more easily from negatively charged CNTs which is followed by uncharged and positively charged ones. It is further shown that the presence of functional groups leads to enhancing the operating frequency of such oscillatory systems especially when the electric charges of ion and functional groups have different signs.

  2. Determination of chloride in brazilian crude oils by ion chromatography after extraction induced by emulsion breaking.

    Science.gov (United States)

    Robaina, Nicolle F; Feiteira, Fernanda N; Cassella, Alessandra R; Cassella, Ricardo J

    2016-08-01

    The present paper reports on the development of a novel extraction induced by emulsion breaking (EIEB) method for the determination of chloride in crude oils. The proposed method was based on the formation and breaking of oil-in-water emulsions with the samples and the consequential transference of the highly water-soluble chloride to the aqueous phase during emulsion breaking, which was achieved by centrifugation. The determination of chloride in the extracts was performed by ion chromatography (IC) with conductivity detection. Several parameters (oil phase:aqueous phase ratio, crude oil:mineral oil ratio, shaking time and type and concentration of surfactant) that could affect the performance of the method were evaluated. Total extraction of chloride from samples could be achieved when 1.0g of oil phase (0.5g of sample+0.5g of mineral oil) was emulsified in 5mL of a 2.5% (m/v) solution of Triton X-114. The obtained emulsion was shaken for 60min and broken by centrifugation for 5min at 5000rpm. The separated aqueous phase was collected, filtered and diluted before analysis by IC. Under these conditions, the limit of detection was 0.5μgg(-1) NaCl and the limit of quantification was 1.6μgg(-1) NaCl. We applied the method to the determination of chloride in six Brazilian crude oils and the results did not differ statistically from those obtained by the ASTM D6470 method when the paired Student-t-test, at 95% confidence level, was applied.

  3. Diffusion of Chloride Ions in Soils:Ⅱ.Kinetic and Ther—modynamic Characteristics

    Institute of Scientific and Technical Information of China (English)

    XUMINGGANG; ZHANGYIPING; 等

    1997-01-01

    The amounts of chloride ions diffused in four soils of different textures at the same water content under different temperature and at varied time were measured by the diffusion cell method using 36Cl-labelled CaCl2 solution,Five kinetic models were used to fit the dynamic process of the diffusion of chloride ions in the soils ,It was found that Elovich equation or power function equation was the best model to describe the process .The pseudothermodynamic parameters,i.e.the net reaction energy,the activation entropy, activation enthalpy and activation free energy of the diffusion,were dervied from the absolute reaction-rate theory.The results showed that these parameters decreased in the order of loessal soil>black lu soil> lou soil> yellow cinnamon soil,which indicated that the force an the heat-energy barrier to be overcome for diffusion decreased ,the diffusion rate increased and the disorder of the soil-solution-ion system due to diffusion decreased successively with the texture becoming heavier in the four soils.

  4. The Effects of Calcium Ions on the Flotation of Sillimanite Using Dodecylammonium Chloride

    Directory of Open Access Journals (Sweden)

    Zhijie Chen

    2017-02-01

    Full Text Available The effects of Ca2+ ions on the flotation of sillimanite using dodecylammonium chloride as a collector were investigated by micro-flotation tests, zeta potential measurements, solution chemistry analysis and molecular dynamics (MD simulation. The micro-flotation results indicated that Ca2+ ions remarkably inhibit the flotation of sillimanite in the pH range of 2.0–9.0. The point of zero charge (PZC of sillimanite changed from 5.4 to 6.1 with the addition of Ca2+ ions. Meanwhile, the calculated concentration of RNH3+ in the sillimanite interface layer decreased in the presence of Ca2+ ions. The results of MD simulation revealed that Ca2+ ions have strong binding energy with the sillimanite (010 surface, and the binding energy of RNH3+ with sillimanite (010 surface reduced in the presence of Ca2+ ions. The conclusions drawn from the computations are in good agreement with the experimental results.

  5. Evidence for a channel for the electrogenic transport of chloride ion in the rat hepatocyte

    Energy Technology Data Exchange (ETDEWEB)

    Bear, C.E.; Petrunka, C.N.; Strasberg, S.M.

    1985-05-01

    Chloride is the major inorganic anion in bile but its mechanism of passage from blood to bile is uncertain. Specific membrane channels account for most net inorganic anion flux in other cell types such as the proximal tubular cell and red blood cell; disulfonic stilbenes inhibit anion movement through these channels. Therefore, we have sought the presence of similar channels in the hepatocyte. Net inorganic anion flux or conductance was initiated in isolated rat hepatocytes by valinomycin in the presence of an outward potassium gradient. Potassium concentration in the extracellular medium increased from 2.75 +/- 0.02 in control cell suspensions to 3.15 +/- 0.04 in valinomycin-treated cell suspensions. Membrane potential difference (Em) (mV), determined as the distribution of (/sup 14/C)tetraphenyl phosphonium ion was -28 mV in control cells and -42 mV in valinomycin-treated cells. Intracellular chloride concentration (/sup 36/Cl-) (mEq per liter of cell water) decreased significantly from 38.6 in control cells to 32.0 in valinomycin-treated cells. The observed intracellular concentrations (/sup 36/Cl-) in both control and valinomycin-treated cell suspensions closely approximates values predicted on the basis of the Nernst equation: 41 and 29 (mEq per liter of cell water), respectively, suggesting that the chloride ion is passively distributed on the basis of the membrane potential difference. Furthermore, net rate-limited cell water loss of approximately 15% of control values was associated with the above valinomycin-stimulated changes in ion distribution, as assessed using three methods of cell water volume determination.

  6. Copper electrodeposition from cuprous chloride solutions containing lead, zinc or iron ions

    Institute of Scientific and Technical Information of China (English)

    M. Tchoumou; M. Roynette Ehics

    2005-01-01

    Cuprous chloride hydrochloric acid solutions were electrolysed in a two compartments cell without agitation for copper extraction. It is found that the current density affects the colour and the size of copper deposits. During electrodeposition of copper from cuprous solution in the presence of various concentrations of lead, zinc or iron ions at different current densities, it is observed that lead is codeposited with copper by increasing current density.In all experiments, the current efficiency for the copper deposition reaction fluctuates between 88.50% and 95.50%.

  7. Corrosion of Carbon Steel and Corrosion-Resistant Rebars in Concrete Structures Under Chloride Ion Attack

    Science.gov (United States)

    Mohamed, Nedal; Boulfiza, Mohamed; Evitts, Richard

    2013-03-01

    Corrosion of reinforced concrete is the most challenging durability problem that threatens reinforced concrete structures, especially structures that are subject to severe environmental conditions (i.e., highway bridges, marine structures, etc.). Corrosion of reinforcing steel leads to cracking and spalling of the concrete cover and billions of dollars are spent every year on repairing such damaged structures. New types of reinforcements have been developed to avoid these high-cost repairs. Thus, it is important to study the corrosion behavior of these new types of reinforcements and compare them to the traditional carbon steel reinforcements. This study aimed at characterizing the corrosion behavior of three competing reinforcing steels; conventional carbon steel, micro-composite steel (MMFX-2) and 316LN stainless steel, through experiments in carbonated and non-carbonated concrete exposed to chloride-laden environments. Synthetic pore water solutions have been used to simulate both cases of sound and carbonated concrete under chloride ions attack. A three-electrode corrosion cell is used for determining the corrosion characteristics and rates. Multiple electrochemical techniques were applied using a Gamry PC4™ potentiostat manufactured by Gamry Instruments (Warminster, PA). DC corrosion measurements were applied on samples subjected to fixed chloride concentration in the solution.

  8. Functional modifications of acid-sensing ion channels by ligand-gated chloride channels.

    Directory of Open Access Journals (Sweden)

    Xuanmao Chen

    Full Text Available Together, acid-sensing ion channels (ASICs and epithelial sodium channels (ENaC constitute the majority of voltage-independent sodium channels in mammals. ENaC is regulated by a chloride channel, the cystic fibrosis transmembrane conductance regulator (CFTR. Here we show that ASICs were reversibly inhibited by activation of GABA(A receptors in murine hippocampal neurons. This inhibition of ASICs required opening of the chloride channels but occurred with both outward and inward GABA(A receptor-mediated currents. Moreover, activation of the GABA(A receptors modified the pharmacological features and kinetic properties of the ASIC currents, including the time course of activation, desensitization and deactivation. Modification of ASICs by open GABA(A receptors was also observed in both nucleated patches and outside-out patches excised from hippocampal neurons. Interestingly, ASICs and GABA(A receptors interacted to regulate synaptic plasticity in CA1 hippocampal slices. The activation of glycine receptors, which are similar to GABA(A receptors, also modified ASICs in spinal neurons. We conclude that GABA(A receptors and glycine receptors modify ASICs in neurons through mechanisms that require the opening of chloride channels.

  9. Electrochemical corrosion behavior of Cu-40Ni-20Cr alloys with different grain sizes in solutions containing chloride ions

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The electrochemical corrosion behavior of the two Cu-40Ni-20Cr alloys prepared by conventional casting(CA) and mechanical alloying(MA) with the different grain sizes was studied by using open-circuit potential(OCP), potentiodynamic polarization and electrochemical impedance spectroscopy(EIS) methods in solutions containing chloride ions. The results show that the free corrosion potentials of the two alloys move towards negative values, corrosion currents increase and therefore corrosion rates become faster with the increase of chloride ion concentrations. EIS plots of CACu-40Ni-20Cr alloy are composed of single capacitive loop, while EIS plots of MACu-40Ni-20Cr alloy are composed of double capacitive loops in solution containing lower chloride ion concentrations. EIS plots of the two alloys have Warburg impedance with the increase of chloride ion concentrations.Corrosion rates of MACu-40Ni-20Cr alloy become faster than those of CACu-40Ni-20Cr alloy obviously in solutions containing the same chloride ion concentrations because MACu-40Ni-20Cr alloy is able to produce large concentrations of grain boundaries in the course of reduction in grain size by mechanical alloying.

  10. Geometric isotope effects on small chloride ion water clusters with path integral molecular dynamics simulations

    Science.gov (United States)

    Wang, Qi; Suzuki, Kimichi; Nagashima, Umpei; Tachikawa, Masanori; Yan, Shiwei

    2013-11-01

    The geometric isotope effects on the structures of hydrated chloride ionic hydrogen bonded clusters are explored by carrying out path integral molecular dynamics simulations. First, an outer shell coordinate is selected to display the rearrangement of single and multi hydration shell cluster structures. Next, to show the competition of intramolecular and intermolecular nuclear quantum effects, the intramolecular OH∗ stretching and intermolecular ion-water wagging motions are studied for single and multi shell structures, respectively. The results indicate that the intermolecular nuclear quantum effects stabilize the ionic hydrogen bonds in single shell structures, while they are destabilized through the competition with intramolecular nuclear quantum effects in multi shell structures. In addition, the correlations between ion-water stretching motion and other cluster vibrational coordinates are discussed. The results indicate that the intermolecular nuclear quantum effects on the cluster structures are strongly related to the cooperation of the water-water hydrogen bond interactions.

  11. Hydrogen ion-selective poly(vinyl chloride) membrane electrode based on a calix[4]arene.

    Science.gov (United States)

    Kuruoğlu, Demet; Canel, Esin; Memon, Shahabuddin; Yilmaz, Mustafa; Kiliç, Esma

    2003-02-01

    A hydrogen ion-selective poly(vinyl chloride) membrane electrode was constructed using 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetracyanomethoxycalix[4]arene as a neutral carrier. The electrode showed an apparent Nernstian response in the 2-11.5 pH range with a slope of 54.0 +/- 0.2 mV/pH at 20 +/- degrees C. This electrode showed a rapid response of the emf to changes in the pH, high ion selectivity with respect to lithium, sodium and potassium, and characteristics similar to those reported for the conventional pH glass membrane electrode. It can be used as a potentiometric indicator electrode in hydrofluoric acid solutions. The effects of iodide, thiocyanate, perchlorate and bromide on the characteristics of the electrode were also considered.

  12. Removal of potassium chloride by nanofiltration from ion-exchanged solution containing potassium clavulanate.

    Science.gov (United States)

    Kim, Hyun Han; Kim, Jae Hyung; Chang, Yong Keun

    2010-01-01

    In this study, nanofiltration with NF200 membrane was employed to remove KCl from ion-exchanged solutions containing potassium clavulanate. The pore radius of NF200 membrane was estimated to be around 0.39 nm. The effects of operating pressure on separation performance were investigated in a range of 100-400 psig. The influences of cross-flow velocity (0.14-0.70 cm/s), temperature (4-25 degrees C), and feed composition were also investigated. In all experiments, clavulanate rejection showed high levels from 0.91 to 0.99, while chloride rejection ranged from 0.06 to 0.54. In a case at an operating pressure of 50 psig and 25 degrees C, as much as 94% of clavulanate was retained while 94% of chloride was removed, indicating that NF200 membrane was a suitable choice for selectively removing KCl. NF200 membrane also showed a stable performance in the operational stability test with an ion-exchanged solution obtained by treating actual fermentation broth.

  13. A chloride ion nanosensor for time-resolved fluorimetry and fluorescence lifetime imaging.

    Science.gov (United States)

    Ruedas-Rama, Maria J; Orte, Angel; Hall, Elizabeth A H; Alvarez-Pez, Jose M; Talavera, Eva M

    2012-03-21

    In this work, the first CdSe/ZnS quantum dot (QD) photoluminescence lifetime based chloride ion nanosensor is reported. The acridinium dication lucigenin was self-assembled on the surface of negatively charged mercaptopropionic acid capped QDs to achieve QD-lucigenin conjugates. Upon attachment, a drastic decrease of the photoluminescence lifetime of both QD nanoparticles and lucigenin is observed by virtue of a charge transfer mechanism. Since lucigenin is a chloride-sensitive indicator dye, the photoluminescence decay of QD-lucigenin conjugates changes by adding chloride ion. The photoluminescence lifetime of the QDs in the conjugate increases after reacting with Cl(-), but also shows a concomitant decrease in the lucigenin lifetime immobilized on the surface. The photoluminescence lifetime of QD-lucigenin nanosensors shows a linear response in the Cl(-) concentration range between 0.5 and 50 mM. Moreover, the ratio τ(ave)(QD)/τ(ave)(luc) can be used as an analytical signal since the lifetime ratio presents a linear response in the same Cl(-) concentration range. The system also shows good selectivity towards most of the main anions and molecules that can be found in biological fluids. These nanosensors have been satisfactorily applied for Cl(-) determination in simulated intracellular media with high sensitivity and high selectivity. Finally, we demonstrate the potential application of the proposed nanosensor in confocal fluorescence lifetime imaging (FLIM). These results show the promising application of the QD-lucigenin nanosensors in FLIM, particularly for intracellular sensing, with the invaluable advantages of the time-resolved fluorescence techniques.

  14. Development of a Poly(vinyl chloride)-based Nitrate Ion-selective Electrode

    Institute of Scientific and Technical Information of China (English)

    HE Meng-meng; YANG Hui-zhong

    2012-01-01

    The authors developed a nitrate ion-selective electrode(ISE) based on poly(vinyl chloride)(PVC) membrane with methyltrioctylammonium nitrate as a carrier and 1-decanol as a plasticizer.The performance of the nitrate-sensitive membranes was optimized by tuning the composition of components.The electrode exhibits a linear response with a Nernstian slope of (52±1.0) mV per decade for the nitrate ion concentration ranging from 5.8×10-5 mol/L to 1.0 mol/L.The electrode can be used to detect a low concentration of nitrate ions down to 3 × 10-5 mol/L in a pH range of 2.1-11.5 without any compensation.The advantage of the electrode includes simple preparation,short response time and good repeatability.The detection performance of the novel electrode on nitrate ions has been tested for water samples.

  15. Involvements of chloride ion in decolorization of Acid Orange 7 by activated peroxydisulfate or peroxymonosulfate oxidation

    Institute of Scientific and Technical Information of China (English)

    Ping Wang; Shiying Yang; Liang Shan; Rui Niu; Xueting Shao

    2011-01-01

    The effects of chloride anion (C1-) (up to 1.0 mol/L) on the decolorization of a model compound,azo dye Acid Orange 7 (AO7),by sulfate radical (SO4-*) based-peroxydisulfate (PS) or peroxymonosulfate (PMS) oxidation under various activated conditions (UV254 nm/PS,Thermal (70℃/PS,UV254 nm/PMS,Co2+/PMS) were investigated.Methanol and NH4+ were used as quenching reagents to determine the contributions of active chlorine species (dichloride radical (Cl2-*) and hypochlorous acid (HClO)).The results indicated that the effects of Cl- on the reaction mechanism were different under various activated conditions.For UV/PS and Thermal/PS,the inhibition tendency became more clear as the Cl-concentration increased,probably due to the reaction between Cl- and SO4-* and the generation of Cl2-* or HClO.For UV/PMS,Cl- did not exhibit inhibition when the concentration was below 0.1 mol/L.As Cl-concentration reached to 1.0 mol/L,the decolorization rate of AO7 was,however,accelerated,possibly because PMS directly reacts with C1- to form HC1O.For Co2+/PMS,Cl- exhibited a significant inhibiting effect even at low concentration (≤ 0.01 mol/L).When Cl- concentration exceeded 0.1 mol/L,the activation of PMS by Co2+ was almost completely inhibited.Under this condition,HClO maybe played a major role in decolorization of AO7.The results implicated that chloride ion is an important factor in SO4-*-based degradation of organic contamination in chloride-containing water.

  16. Evaluation of the method of electrochemical extraction of chlorides ions for the rehabilitation of concrete structures with reinforcement corrosion problems

    Directory of Open Access Journals (Sweden)

    Monteiro, E.

    2003-12-01

    Full Text Available The present work evaluates the method of electrochemical extraction of chloride ions for the rehabilitation of corroded concrete structures. The influence of the concrete cover and the water-to-cement ratio in the efficiency of the method was studied by determining the initial and the final chloride content. Electrochemical impedance spectroscopy and the corrosion potential were used to monitor the reinforcement electrochemical behavior during the chloride extraction. The test results verify that this method successfully extracted chloride ions like it was previous reported in the literature. On average, this method removed 77% of the content of initial chloride ions at a distance of 0.5 cm from the surface and 50% of the content of initial chloride ions near de rebars.

    El actual trabajo evalúa el método de extracción electroquímica de cloruros para la rehabilitación de estructuras de hormigón corroídas. La influencia del espesor de recubrimiento y de la relación agua/cemento en la eficacia del método fue estudiada determinando el contenido inicial y final de cloruros. La técnica de impedancia electroquímica y el potencial de la corrosión fueron utilizados para la monitorización del comportamiento electroquímico del refuerzo durante la extracción de cloruros. Los resultados de los ensayos verificaron que este método extrajo con éxito cloruros, tal y como fue divulgado previamente en la literatura. Como promedio, este método extrajo el 77% del contenido de iones iniciales de cloruros a una distancia de 0,5 centímetros de la superficie, y el 50% del contenido de cloruros cerca de las armaduras.

  17. Chloride-Ion Penetrability and Mechanical Analysis of High Strength Concrete with Copper Slag

    Directory of Open Access Journals (Sweden)

    Savaş Erdem

    2014-05-01

    Full Text Available The use of waste materials and industrial by-products in high-strength concrete could increase the sustainability of the construction industry. In this study, the potential of using copper slag as coarse aggregate in high-strength concrete was experimentally investigated. The effects of replacing gravel coarse aggregate by copper slag particles on the compressive strength, chloride ion- migration, water permeability and impact resistance of high-strength concretes were evaluated. Incorporating copper slag coarse particles resulted in a compressive strength increase of about 14 % on average partly due to the low Ca/Si ratio through the interface area of this concrete (more homogenous internal structure as confirmed by the energy dispersive X-ray micro chemical analysis. It was also found that the copper slag high-strength concrete provided better ductility and had much greater load carrying capacity compared to gravel high-strength concrete under dynamic conditions. Finally, it was observed that in comparison to the high strength concrete with slag, the chloride migration coefficient from non-steady state migration was approximately 30 % greater in the gravel high-strength concrete.

  18. Influence of chloride ion concentration on immersion corrosion behaviour of plasma sprayed alumina coatings on AZ31B magnesium alloy

    Directory of Open Access Journals (Sweden)

    D. Thirumalaikumarasamy

    2014-12-01

    Full Text Available Corrosion attack of aluminium and magnesium based alloys is a major issue worldwide. The corrosion degradation of an uncoated and atmospheric plasma sprayed alumina (APS coatings on AZ31B magnesium alloy was investigated using immersion corrosion test in NaCl solutions of different chloride ion concentrations viz., 0.01 M, 0.2 M, 0.6 M and 1 M. The corroded surface was characterized by an optical microscope and X-ray diffraction. The results showed that the corrosion deterioration of uncoated and coated samples were significantly influenced by chloride ion concentration. The uncoated magnesium and alumina coatings were found to offer a superior corrosion resistance in lower chloride ion concentration NaCl solutions (0.01 M and 0.2 M NaCl. On the other hand the coatings and Mg alloy substrate were found to be highly susceptible to localized damage, and could not provide an effective corrosion protection in solutions containing higher chloride concentrations (0.6 M and 1 M. It was found that the corrosion resistance of the ceramic coatings and base metal gets deteriorated with the increase in the chloride concentrations.

  19. Chloride uptake and base secretion in freshwater fish: a transepithelial ion-transport metabolon?

    Science.gov (United States)

    Tresguerres, Martin; Katoh, Fumi; Orr, Elizabeth; Parks, Scott K; Goss, Greg G

    2006-01-01

    Despite all the efforts and technological advances during the last few decades, the cellular mechanisms for branchial chloride uptake in freshwater (FW) fish are still unclear. Although a tight 1 : 1 link with HCO-3 secretion has been established, not much is known about the identity of the ion-transporting proteins involved or the energizing steps that allow for the inward transport of Cl- against the concentration gradient. We propose a new model for Cl- uptake in FW fish whereby the combined action of an apical anion exchanger, cytoplasmic carbonic anhydrase, and basolateral V-type H+ -ATPase creates a local [HCO-3] high enough to energize Cl- uptake. Our model is based on analyses of structure-function relationships, reinterpretation of previous results, and novel observations about gill cell subtypes and immunolocalization of the V-H+ -ATPase.

  20. IR study on the effect of chloride ion on porous silicon

    Science.gov (United States)

    Sreejith, K.; Pillai, C. G. S.

    2006-10-01

    Infrared (IR) studies have been carried out on porous silicon samples to infer on the changes in the surface bonding in the porous silicon (PS) layer due to chloride (Cl -) and subsequent fluoride (F -) ion exposures with respect to time. It is observed that silicon hydride linkages decreases and silicon oxide linkages increases with time of exposure to HCl, suggesting a possible oxidation of the porous layer. IR study revealed the formation of Si dbnd O (silanones) bonds. A possible mechanism for the formation of silanones from Si sbnd OH species has been proposed to explain the observation. We also observed a saturation of silicon oxide groups with complete disappearance of silicon hydride peaks indicating the complete conversion of silicon hydride to oxides. Furthermore on exposure to F -, the IR spectrum showed a rapid destruction of silicon oxygen linkages.

  1. An Accelerated Test Method of Simultaneous Carbonation and Chloride Ion Ingress: Durability of Silica Fume Concrete in Severe Environments

    Directory of Open Access Journals (Sweden)

    S. A. Ghahari

    2016-01-01

    Full Text Available The effects of simultaneous carbonation and chloride ion attack on mechanical characteristics and durability of concrete containing silica fume have been investigated through an accelerated test method. Specimens containing different amounts of silica fume were maintained in an apparatus in which carbon dioxide pressure and concentration and relative humidity were kept constant, and wetting and drying cycles in saline water were applied. Surface resistivity, sorptivity, CO2 consumption, and carbonation and chloride ion ingress depths measurements were taken. Phase change due to carbonation and chloride ion attack was monitored by XRD analysis, and microstructures and interfacial transition zones were studied by implementing SEM as well as mercury intrusion porosimetry. It was expected to have a synergistic effect in the tidal zone where simultaneous carbonation and chloride ion attack happen. However, the observed reduced surface resistivity, compared to specimens maintained in CO2 gas, could be due to the moisture that is available near the surface, hindering CO2 from penetrating into the pores of the specimens. Moreover, the porosity analysis of the specimens showed that the sample containing silica fume cured in the tidal zone had 50.1% less total porosity than the plain cement paste cured in the same condition.

  2. Ion chromatography for the precise analysis of chloride and sodium in sweat for the diagnosis of cystic fibrosis

    NARCIS (Netherlands)

    Doorn, J.; Storteboom, T. T. R.; Mulder, A. M.; de Jong, W. H. A.; Rottier, B. L.; Kema, I. P.

    2015-01-01

    BACKGROUND: Measurement of chloride in sweat is an essential part of the diagnostic algorithm for cystic fibrosis. The lack in sensitivity and reproducibility of current methods led us to develop an ion chromatography/high-performance liquid chromatography (IC/HPLC) method, suitable for the analysis

  3. Chloride ion-catalyzed generation of difluorocarbene for efficient preparation of gem-difluorinated cyclopropenes and cyclopropanes

    KAUST Repository

    Wang, Fei

    2011-01-01

    A chloride ion-catalyzed generation of difluorocarbene from a relatively non-toxic and inexpensive precursor, Me3SiCF2Cl (1), under mild and neutral conditions leads to an efficient preparation of gem-difluorocyclopropenes and difluorocyclopropanes through [2 + 1] cycloaddition reactions with alkynes and alkenes, respectively. © 2011 The Royal Society of Chemistry.

  4. Establishment of the conditions for the determination of the concentration of the uranyl ion in perchloric media by Fluorescence; Establecimiento de las condiciones para la determinacion de la concentracion del ion uranilo en medio perclorico por Fluorescencia

    Energy Technology Data Exchange (ETDEWEB)

    Contreras R, A.; Ordonez R, E.; Fernandez V, S.M. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)]. e-mail: contraida@yahoo.com.mx

    2004-07-01

    The influence of the p H is reported in the spectra of luminescence of the ion uranyl in sodium perchlorate 2M. The best spectra were observed to ph <3 that to neutral and basic p Hs this is explained by the present species. They were carried out four calibration curves for the uranyl in perchloric acid media, taking into account the area under the curve, the maximum height of two characteristic peaks of this ion, in those that one observes a better correlation with the maximum height of the peak located to 486.7 nm. (Author)

  5. Silver release from nanocomposite Ag/alginate hydrogels in the presence of chloride ions: experimental results and mathematical modeling

    Science.gov (United States)

    Kostic, Danijela; Vidovic, Srđan; Obradovic, Bojana

    2016-03-01

    A stepwise experimental and mathematical modeling approach was used to assess silver release from nanocomposite Ag/alginate microbeads in wet and dried forms into water and into normal saline solution chosen as a simplified model for certain biological fluids (e.g., blood plasma, wound exudates, sweat, etc). Three phenomena were connected and mathematically described: diffusion of silver nanoparticles (AgNPs) within the alginate hydrogel, AgNP oxidation/dissolution and reaction with chloride ions, and diffusion of the resultant silver-chloride species. Mathematical modeling results agreed well with the experimental data with the AgNP diffusion coefficient estimated as 1.3 × 10-18 m2 s-1, while the first-order kinetic rate constant of AgNP oxidation/dissolution and diffusivity of silver-chloride species were shown to be inversely related. In specific, rapid rehydration and swelling of dry Ag/alginate microbeads induced fast AgNP oxidation/dissolution reaction with Cl- and AgCl precipitation within the microbeads with the lowest diffusivity of silver-chloride species compared to wet microbeads in normal saline. The proposed mathematical model provided an insight into the phenomena related to silver release from nanocomposite Ca-alginate hydrogels relevant for use of antimicrobial devices and established, at the same time, a basis for further in-depth studies of AgNP interactions in hydrogels in the presence of chloride ions.

  6. Physiological implications of the regulation of vacuolar H+-ATPase by chloride ions

    Directory of Open Access Journals (Sweden)

    L.R. Carraro-Lacroix

    2009-02-01

    Full Text Available Vacuolar H+-ATPase is a large multi-subunit protein that mediates ATP-driven vectorial H+ transport across the membranes. It is widely distributed and present in virtually all eukaryotic cells in intracellular membranes or in the plasma membrane of specialized cells. In subcellular organelles, ATPase is responsible for the acidification of the vesicular interior, which requires an intraorganellar acidic pH to maintain optimal enzyme activity. Control of vacuolar H+-ATPase depends on the potential difference across the membrane in which the proton ATPase is inserted. Since the transport performed by H+-ATPase is electrogenic, translocation of H+-ions across the membranes by the pump creates a lumen-positive voltage in the absence of a neutralizing current, generating an electrochemical potential gradient that limits the activity of H+-ATPase. In many intracellular organelles and cell plasma membranes, this potential difference established by the ATPase gradient is normally dissipated by a parallel and passive Cl- movement, which provides an electric shunt compensating for the positive charge transferred by the pump. The underlying mechanisms for the differences in the requirement for chloride by different tissues have not yet been adequately identified, and there is still some controversy as to the molecular identity of the associated Cl--conducting proteins. Several candidates have been identified: the ClC family members, which may or may not mediate nCl-/H+ exchange, and the cystic fibrosis transmembrane conductance regulator. In this review, we discuss some tissues where the association between H+-ATPase and chloride channels has been demonstrated and plays a relevant physiologic role.

  7. Determination of the stability of the uranyl ion sipped in {tau}-hydrogen phosphate of zirconium in sodic form; Determinacion de la estabilidad del ion uranilo sorbido en {tau}-hidrogenofosfato de zirconio en forma sodica

    Energy Technology Data Exchange (ETDEWEB)

    Ordonez R, E.; Fernandez V, S.M. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Drot, R.; Simoni, E. [Universite de Paris-Sud-XI, Institut de Physique Nucleaire d' Orsay, Groupe de radiochimie, Bat. 100, 91406 Orsay (France)]. e-mail: edo@nuclear.inin.mx

    2005-07-01

    The stability of the uranyl sipped in the zirconium {tau}-hydrogen phosphate in sodic form ({tau}-NaZrP), was carried out characterizing the complexes formed by Laser spectroscopy in the visible region and by X-ray photoelectron spectroscopy. The material was prepared by a new synthesis technique working in nitrogen atmosphere and to low temperatures. The sorption of the uranyl ion was made in acid media with concentrations of 10{sup -4} and 10{sup -5} of uranyl nitrate and with ion forces of 0.1 and 0.5 M of NaClO{sub 4}. The spectra of induced fluorescence with laser (TRLFS) show that the uranyl is fixed in very acid media in three well differentiated species, to pH less acid, the specie of long half life disappears and are only those of short half life. The results of the binding energy obtained by XPS indicate that the binding energy of the uranyl confer it a stable character to the complex formed in the {tau}-NaZP, that makes to this material appropriate to retain to the uranyl in solution to high ion forces and in acid media. (Author)

  8. 离子色谱法测定土壤中的Cl-和SO42-%Determination of Chloride Ion and Sulfate Ion in Soil by Ion Chromatography

    Institute of Scientific and Technical Information of China (English)

    徐秀丽; 刘文全; 徐兴永; 马恭博

    2014-01-01

    Ion chromatography was used to detect chloride ion and sulfate ion in soil. The mixture of 2.0 mmol/L sodium carbonate and 1.3 mmol/L sodium bicarbonate solution was selected to be mobile phase, and the flow rate was 2 mL/min. In such circumstances, the retention time of chloride ion was 1.96 min, sulfate ion was about 12.26 min. A good linear relationship was obtained between the mass concentration and the chromatograph parameter in the range of 8-10 mg/L Cl-and 10-30 mg/L SO42-, the linear correlation coefficients were 0.999 4 and 0.999 7, the recovery rates were 93.8%and 105.4%, respectively. The measuring relative standard deviation were all less than 1%(n=6). The method was suitable for the determination of Cl-and SO42-in soil.%采用离子色谱法测定土壤浸提液中的Cl-和SO42-。选择2.0 mmol/L Na2CO3-1.3 mmol/L NaHCO3混合液为淋洗液,流速为2 mL/min,在此条件下,Cl-保留时间为1.96 min,SO42-保留时间约为12.26 min,Cl-,SO42-的质量浓度分别在2~8,10~30 mg/L范围内与色谱参数线性相关,相关系数分别为0.9994和0.9997,Cl-,SO42-的平均加标回收率分别为93.8%,105.4%,测量结果的相对标准偏差均小于1%(n=6)。该法适用于土壤中Cl-和SO42-的测定。

  9. Ion mobility spectrometry as a fast analytical tool in benzalkonium chloride homologs determination.

    Science.gov (United States)

    Gallart-Mateu, D; Armenta, S; Esteve-Turrillas, F A; de la Guardia, M

    2017-03-01

    A novel procedure is proposed for the determination by ion mobility spectrometry (IMS) of C12, C14 and C16 benzalkonium chloride (BAC) homologs. The proposed method requires minimum sample treatment and the measurement was made in less than one minute. A high sensitivity was obtained for BAC determination by IMS with limit of detection values from 37 to 69µgL(-1). Accuracy of the proposed methodology was evaluated through the analysis of aqueous and alcoholic samples spiked with BAC at concentration levels from 0.002% to 20% (w/v), providing recovery values from 91% to 104%. BAC was determined in sanitary alcohols, nasal sprays, postharvest products, algaecides, and treated swimming pool water. Results obtained by the proposed IMS methodology were statistically comparable to those provided by a liquid chromatography-ultraviolet (LC-UV) reference methodology. The Green Certificate evaluation of the proposed IMS methodology provided 91 score points in the Eco-Scale as compared with 77 for LC-UV method.

  10. Sodium Chloride interaction with solvated and crystalline cellulose : sodium ion affects the tetramer and fibril in aqueous solution

    OpenAIRE

    Bellesia, Giovanni; Gnanakaran, S.

    2013-01-01

    Inorganic salts are a natural component of biomass which have a significant effect on the product yields from a variety of biomass conversion processes. Understanding their effect on biomass at the microscopic level can help discover their mechanistic role. We present a study of the effect of aqueous sodium chloride (NaCl) on the largest component of biomass, cellulose, focused on the thermodynamic and structural effect of a sodium ion on the cellulose tetramer, and fibril. Replica exchange m...

  11. Compressive Strength, Pore Size Distribution and Chloride-ion Penetration of Recycled Aggregate Concrete Incorporating Class-F Fly Ash

    Institute of Scientific and Technical Information of China (English)

    KOU Shicong; C S Poon

    2006-01-01

    The effects of fly ash on the compressive strength, pore size distribution ard chloride-ion penetration of recycled aggregate concrete were investigated. Two series of concrete mixtures were prepared. The concrete mixtures in series I had a water-to-binder ratio and a cement content of 0.55 and 410 kg/m3 , respectively. The concrete mixtures in series Ⅱ had a water-to-binder ratio and a cement content of 0.45 and 400 kg/m3 respectively. Recycled aggregate was used as 20% , 50% , and 100% replacements of natural coarse aggregate in the concrete mixtures in both series. In addition, fly ash was used as 0% , 25% and 35% by weight replacements of cement. The results show that the compressive strengths of the concrete decreased as the recycled aggregate and the fly ash contents increased. The total porosity and average porosity diameter of the concrete increased as the recycled aggregate content increased. Furthermore, an increase in the recycled aggregate content decreased the resistance to chloride ion penetration. Nevertheless, the replacement of cement by 25% fly ash improved the resistance to chloride ion penetration and pore diameters and reduced the total porosity of the recycled aggregate concrete.

  12. Effects of anodic potential and chloride ion on overall reactivity in electrochemical reactors designed for solar-powered wastewater treatment.

    Science.gov (United States)

    Cho, Kangwoo; Qu, Yan; Kwon, Daejung; Zhang, Hao; Cid, Clément A; Aryanfar, Asghar; Hoffmann, Michael R

    2014-02-18

    We have investigated electrochemical treatment of real domestic wastewater coupled with simultaneous production of molecular H2 as useful byproduct. The electrolysis cells employ multilayer semiconductor anodes with electroactive bismuth-doped TiO2 functionalities and stainless steel cathodes. DC-powered laboratory-scale electrolysis experiments were performed under static anodic potentials (+2.2 or +3.0 V NHE) using domestic wastewater samples, with added chloride ion in variable concentrations. Greater than 95% reductions in chemical oxygen demand (COD) and ammonium ion were achieved within 6 h. In addition, we experimentally determined a decreasing overall reactivity of reactive chlorine species toward COD with an increasing chloride ion concentration under chlorine radicals (Cl·, Cl2(-)·) generation at +3.0 V NHE. The current efficiency for COD removal was 12% with the lowest specific energy consumption of 96 kWh kgCOD(-1) at the cell voltage of near 4 V in 50 mM chloride. The current efficiency and energy efficiency for H2 generation were calculated to range from 34 to 84% and 14 to 26%, respectively. The hydrogen comprised 35 to 60% by volume of evolved gases. The efficacy of our electrolysis cell was further demonstrated by a 20 L prototype reactor totally powered by a photovoltaic (PV) panel, which was shown to eliminate COD and total coliform bacteria in less than 4 h of treatment.

  13. Chloride transference during electrochemical chloride extraction process

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Chemical titration method and lab-made chloride probes were jointly adopted to investigate the effects of water-to-cement (W/C) ratio and the impressed current density on chloride transport for cement-based materials during electrochemical chloride extraction (ECE) process.The dissolution of bound chlorides and the effect of current density on dissolution were analyzed.The variations of chloride concentration at different depths and the chloride transference process were monitored.Test results show that W/C ratios adopted have slight influence on chloride extraction,while chloride extraction efficiency is mainly determined by the impressed current density.During ECE process a portion of bound chloride ions dissolved and the amount of bound chlorides released is directly proportional to current density.

  14. Studies of removal of palladium(II) ions from chloride solutions on weakly and strongly basic anion exchangers.

    Science.gov (United States)

    Hubicki, Z; Wołowicz, A; Leszczyńska, M

    2008-11-30

    Palladium and its compounds find wide application in industry as a catalytic agent in different manufacture processes. Recovery of precious metals from industrial wastes is difficult and time consuming but in spite of these disadvantages it becomes profitable. Palladium(II) ions sorption from various chloride solutions of the composition: 0.1-6.0M HCl-0.00056 M Pd(II), 1.0M ZnCl(2)-0.1M HCl-0.00056 M Pd(II), 1.0M AlCl(3)-0.1M HCl-0.00056 M Pd(II) on the weakly and strongly basic anion exchangers (Varion ATM, Varion ADM and Varion ADAM) was discussed. The sorption research of Pd(II) ions on these resins was carried out by means of static and dynamic methods. The dynamic processes were applied in order to determine the breakthrough curves of Pd(II) ions. Moreover, the working ion-exchange capacities as well as the weight and bed distribution coefficients were determined from the Pd(II) breakthrough curves. The recovery factors of Pd(II) ions (% R) depending on the phase contact time were obtained by means of static methods. The highest ion-exchange capacities for the 0.1-6.0M HCl-0.00056 M Pd(II) systems were obtained for the weakly basic ion-exchange resin Varion ADAM.

  15. Multiple Osmotic Stress Responses in Acidihalobacter prosperus Result in Tolerance to Chloride Ions

    Science.gov (United States)

    Dopson, Mark; Holmes, David S.; Lazcano, Marcelo; McCredden, Timothy J.; Bryan, Christopher G.; Mulroney, Kieran T.; Steuart, Robert; Jackaman, Connie; Watkin, Elizabeth L. J.

    2017-01-01

    Extremely acidophilic microorganisms (pH optima for growth of ≤3) are utilized for the extraction of metals from sulfide minerals in the industrial biotechnology of “biomining.” A long term goal for biomining has been development of microbial consortia able to withstand increased chloride concentrations for use in regions where freshwater is scarce. However, when challenged by elevated salt, acidophiles experience both osmotic stress and an acidification of the cytoplasm due to a collapse of the inside positive membrane potential, leading to an influx of protons. In this study, we tested the ability of the halotolerant acidophile Acidihalobacter prosperus to grow and catalyze sulfide mineral dissolution in elevated concentrations of salt and identified chloride tolerance mechanisms in Ac. prosperus as well as the chloride susceptible species, Acidithiobacillus ferrooxidans. Ac. prosperus had optimum iron oxidation at 20 g L−1 NaCl while At. ferrooxidans iron oxidation was inhibited in the presence of 6 g L−1 NaCl. The tolerance to chloride in Ac. prosperus was consistent with electron microscopy, determination of cell viability, and bioleaching capability. The Ac. prosperus proteomic response to elevated chloride concentrations included the production of osmotic stress regulators that potentially induced production of the compatible solute, ectoine uptake protein, and increased iron oxidation resulting in heightened electron flow to drive proton export by the F0F1 ATPase. In contrast, At. ferrooxidans responded to low levels of Cl− with a generalized stress response, decreased iron oxidation, and an increase in central carbon metabolism. One potential adaptation to high chloride in the Ac. prosperus Rus protein involved in ferrous iron oxidation was an increase in the negativity of the surface potential of Rus Form I (and Form II) that could help explain how it can be active under elevated chloride concentrations. These data have been used to create a

  16. Charge transfer and polarization for chloride ions bound in ClC transport proteins: natural bond orbital and energy decomposition analyses.

    Science.gov (United States)

    Church, Jonathan; Pezeshki, Soroosh; Davis, Christal; Lin, Hai

    2013-12-19

    ClC transport proteins show a distinct "broken-helix" architecture, in which certain α-helices are oriented with their N-terminal ends pointed toward the binding sites where the chloride ions are held extensively by the backbone amide nitrogen atoms from the helices. To understand the effectiveness of such binding structures, we carried out natural bond orbital analysis and energy decomposition analysis employing truncated active-site model systems for the bound chloride ions along the translocation pore of the EcClC proteins. Our results indicated that the chloride ions are stabilized in such a binding environment by electrostatic, polarization, and charge-transfer interactions with the backbone and a few side chains. Up to ~25% of the formal charges of the chloride ions were found smeared out to the surroundings primarily via charge transfer from the chloride's lone pair n(Cl) orbitals to the protein's antibonding σ*(N-H) or σ*(O-H) orbitals; those σ* orbitals are localized at the polar N-H and O-H bonds in the chloride's first solvation shells formed by the backbone amide groups and the side chains of residues Ser107, Arg147, Glu148, and Tyr445. Polarizations by the chloride ions were dominated by the redistribution of charge densities among the π orbitals and lone pair orbitals of the protein atoms, in particular the atoms of the backbone peptide links and of the side chains of Arg147, Glu148, and Tyr445. The substantial amounts of electron density involved in charge transfer and in polarization were consistent with the large energetic contributions by the two processes revealed by the energy decomposition analysis. The significant polarization and charge-transfer effects may have impacts on the mechanisms and dynamics of the chloride transport by the ClC proteins.

  17. Surface analytical and electrochemical study on the role of adsorbed chloride ions in corrosion of stainless steels

    Energy Technology Data Exchange (ETDEWEB)

    Rossi, A.; Tulifero, R.; Elsener, B. [Cagliari Univ. (Italy). Dept. of Inorganic and Analytical Chemistry

    2001-03-01

    The pitting potential E{sub pit} of 18/8 CrNi stainless steels with different sulfur content (0.003, 0.017 and 0.29%) has been determined from potentiodynamic polarization curves in deaerated neutral solutions (0.1 M NaCl and 1 M Na{sub 2}SO{sub 4} + 0.1 M NaCl) with nominally identical chloride content. E{sub pit} decreased with increasing sulfur content of the alloy and was about 0.2 V more negative in pure 0.1 M NaCl solution. The chemical composition of the passive film and the adsorbed chloride content have been determined by XPS surface analysis on mechanically polished samples passivated for one hour at potentials below the pitting potential. XPS results show that the surface films are composed in all cases of mixed iron-chromium oxi-hydroxides with a higher chromium content than the bulk composition. The average passive film composition (ca. 40% chromium oxi-hydroxide) and the film thickness (2.3 {+-} 0.2 nm) were similar for all 18/8 CrNi steels regardless the different sulfur content. The amount of chlorides in the passive film is about twice as high on steels exposed to pure 0.1 N NaCl solution compared to the mixed 1 M Na{sub 2}SO{sub 4} + 0.1 M NaCl solution. Thus the lower pitting potential measured in pure 0.1 N NaCl solution correlates with the higher amount of chloride ions on the passive film surface. (orig.)

  18. Effect of Fly Ash on Frost-Resistance and Chloride Ions Diffusion Properties of Marine Concrete

    Institute of Scientific and Technical Information of China (English)

    YANG Wen-wu; QIAN Jue-shi; ZHANG Yi-ying

    2009-01-01

    It is necessary to pay more attention to the durability of concrete undergoing freeze-thaw cycles and seawater attack simultaneously.Investigated are the effects of water-binder ratio,fly ash (FA) contents and air-entraining agent on resistance to frost and chloride diffusion of marine concrete blended with FA in natural seawater.The results show that fly ash does not improve the frost resistance of concrete but can improve its resistance to chloride diffusion by addition of less than 30%.The resistance to frost and chloride diffusion of FA concrete can be improved with the decrease of water-binder ratio,and FA may improve both of them simultaneously only being mixed with air-entraining agent.A ratio (named as R) of the frost-resisting durability factor to chloride diffusion coefficient can be used to evaluate the durability of marine concrete.Scanning electron microscope (SEM) analyses are consistent with the evaluations by the value of R.

  19. Regioselective organocatalysis: a theoretical prediction of the selective rate acceleration of the SN2 reaction between an acetate ion and primary alkyl chlorides in DMSO solution.

    Science.gov (United States)

    Pliego, Josefredo R

    2006-05-07

    High level ab initio calculations, including the solvent effect through a continuum solvation model, predict that 1,4-benzenedimethanol is able to catalyse the S(N)2 reaction between an acetate ion and primary alkyl chlorides in dimethyl sulfoxide solution. The catalysis takes place through two selective hydrogen bonds to the transition state. However, for secondary alkyl chlorides the catalysis is not effective due to steric repulsion and desolvation. This effect induces regioselective control of S(N)2 esterification reactions.

  20. Ion-Pair Halogen Bonds in 2-Halo-Functionalized Imidazolium Chloride Receptors: Substituent and Solvent Effects.

    Science.gov (United States)

    Nunes, Rafael; Costa, Paulo J

    2017-01-03

    The interaction of 2-halo-functionalized imidazolium derivatives (n-X(+) ; X=Cl, Br, I) with a chloride anion through ion-pair halogen bonds (n-X⋅Cl) was studied by means of DFT and ab initio calculations. A method benchmark was performed on 2-bromo-1H-imidazol-3-ium in association with chloride (1-Br⋅Cl); MP2 yielded the best results when compared with CCSD(T) calculations. The interaction energies (ΔE) in the gas phase are high and, although the electrostatic interaction is strong owing to the ion-pair nature of the system, large X⋅⋅⋅Cl(-) Wiberg bond orders and contributions from charge transfer (nCl- →σ*C-X) are obtained. These values drop considerably in chloroform and water; this shows that solvent plays a role in modulating the interaction and that gas-phase calculations are particularly unrealistic for experimental applications. The introduction of electron-withdrawing groups in the 4,5-positions of the imidazolium (e.g., -NO2 , -F) increases the halogen-bond strength in both the gas phase and solvent, including water. The effect of the substituents on the 1,3-positions (N-H groups) also depends on the solvent. The variation of ΔE can be predicted through a two-parameter linear regression that optimizes the weights of charge-transfer and electrostatic interactions, which are different in vacuum and in solvent (chloroform and water). These results could be used in the rational design of efficient chloride receptors based on halogen bonds that work in solution, in particular, in an aqueous environment.

  1. Radiotracer studies on ion-selective membranes based on poly(vinyl chloride) matrices.

    Science.gov (United States)

    Jaber, A M; Moody, G J; Thomas, J D; Willcox, A

    1977-10-01

    Radiotracer studies with (45)Ca, (89)Sr and (133)Ba have provided evidence that the permeation of magnesium, strontium and barium ions through PVC membranes containing Orion 92-20-02 liquid ion-exchanger is inhibited by their low affinity for the liquid ion-exchanger sites. Experiments with (7)Be indicate a strong affinity of the membrane for beryllium ions with corresponding inhibition of permeation. When acid is present in the solution on one side of the membrane, preferential permeation by protons may lead to transport of ions against their concentration gradient in order to maintain the balance of charge.

  2. Role of Citrate Ions in the Phosphonate-based Inhibitor System for Mild Steel in Aqueous Chloride Media

    Directory of Open Access Journals (Sweden)

    G. Gunasekaran

    2005-01-01

    Full Text Available The corrosion inhibition efficiency of phosphonic acid and its derivatives for the inhibition of corrosion of mild steel in neutral chloride media is decided by its ability to form protectivefilm over the surface. In this context, the effect of addition of metal cations and certain organic compounds, such as citrate in conjugation with phosphonic acid to impart synergistic corrosion inhibition has been explored. The experiments were carried out using various concentrations of trisodium citrate and zinc ions in an aqueous solution of 2-carboxyethyl phosphonic acid (2CEPA at 25 ppm. The corrosion characteristics have been determined using electrochemical impedance spectroscopy together with determination of corrosion rate by weight-loss method. It has been observed that a combination of inhibitive ions, namely citrate, ZCEPA, and zinc ions at 25 ppm gives 96 per cent inhibition efficiency and this corrosion inhibition is due to the formation of a protective film. By increasing the concentration of citrate beyond 25 ppm, the corrosion inhibition efficiency decreases. This paper discusses the role of citrate and zinc ions in imparting added corrosion inhibition ability using 2CEPA on the basis of experimental results.

  3. Effect of temperature on the durability of class C fly ash belite cement in simulated radioactive liquid waste: Synergy of chloride and sulphate ions

    Energy Technology Data Exchange (ETDEWEB)

    Guerrero, A., E-mail: aguerrero@ietcc.csic.es [Eduardo Torroja Institute for Construction Science (CSIC), C/Serrano Galvache, 4, 28033 Madrid (Spain); Goni, S., E-mail: sgoni@ietcc.csic.es [Eduardo Torroja Institute for Construction Science (CSIC), C/Serrano Galvache, 4, 28033 Madrid (Spain); Allegro, V.R., E-mail: allegro@ietcc.csic.es [Eduardo Torroja Institute for Construction Science (CSIC), C/Serrano Galvache, 4, 28033 Madrid (Spain)

    2009-06-15

    The durability of class C fly ash belite cement (FABC-2-W) in simulated radioactive liquid waste (SRLW) rich in a mixed sodium chloride and sulphate solution is presented here. The effect of the temperature and potential synergic effect of chloride and sulfate ions are discussed. This study has been carried out according to the Koch-Steinegger test, at the temperature of 20 deg. C and 40 deg. C during a period of 180 days. The durability has been evaluated by the changes of the flexural strength of mortar, fabricated with this cement, immersed in a simulated radioactive liquid waste rich in sulfate (0.5 M), chloride (0.5 M) and sodium (1.5 M) ions - catalogued like severely aggressive for the traditional Portland cement - and demineralised water, which was used as reference. The reaction mechanism of sulphate, chloride and sodium ions with the mortar was evaluated by scanning electron microscopy (SEM), porosity and pore-size distribution, and X-ray diffraction (XRD). The results showed that the chloride binding and formation of Friedel's salt was inhibited by the presence of sulphate. Sulphate ion reacts preferentially with the calcium aluminate hydrates forming non-expansive ettringite which precipitated inside the pores; the microstructure was refined and the mechanical properties enhanced. This process was faster and more marked at 40 deg. C.

  4. Effect of temperature on the durability of class C fly ash belite cement in simulated radioactive liquid waste: synergy of chloride and sulphate ions.

    Science.gov (United States)

    Guerrero, A; Goñi, S; Allegro, V R

    2009-06-15

    The durability of class C fly ash belite cement (FABC-2-W) in simulated radioactive liquid waste (SRLW) rich in a mixed sodium chloride and sulphate solution is presented here. The effect of the temperature and potential synergic effect of chloride and sulfate ions are discussed. This study has been carried out according to the Koch-Steinegger test, at the temperature of 20 degrees C and 40 degrees C during a period of 180 days. The durability has been evaluated by the changes of the flexural strength of mortar, fabricated with this cement, immersed in a simulated radioactive liquid waste rich in sulfate (0.5M), chloride (0.5M) and sodium (1.5M) ions--catalogued like severely aggressive for the traditional Portland cement--and demineralised water, which was used as reference. The reaction mechanism of sulphate, chloride and sodium ions with the mortar was evaluated by scanning electron microscopy (SEM), porosity and pore-size distribution, and X-ray diffraction (XRD). The results showed that the chloride binding and formation of Friedel's salt was inhibited by the presence of sulphate. Sulphate ion reacts preferentially with the calcium aluminate hydrates forming non-expansive ettringite which precipitated inside the pores; the microstructure was refined and the mechanical properties enhanced. This process was faster and more marked at 40 degrees C.

  5. Potentiometric Determination of Chloride and Cyanide Ions in Nanoliter Samples with Capillary Indicating Electrodes

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The samples of 25 nL of chloride and cyanide were determined with a kind of glass capillary indicating electrodes by potentiometry. Silver was deposited by the silver-mirror reaction on the inner surface of the glass capillary with a volume of 25 nL. The AgCl film and the AgI film were formed by the treatment of the capillary with a FeCl3 solution and further with a KI solution. The samples were collected automatically into the capillary by the capillary ascension. The procedure in the measurement was merely to place a reference electrode and a capillary indicating electrode vertically on a strip filter paper containing a 0.1 mol/L NaNO3 solution. The various i.d. of the capillary electrodes were used to determine samples ranging from 25 nL to dozens of microliters. The ranges of the linear response to chloride and cyanide were 3.2×10-4-2.2×10-1 mol/L and 1.0×10-5-1.0×10-1 mol/L with an average slope of 55.2 and 52-62 mV/decade, respectively. The samples with various concentrations of chloride and cyanide were determined, and the relative standard deviations were less than 7%.

  6. Understanding the interaction between trivalent lanthanide ions and stereoregular polymethacrylates through luminescence, binding isotherms, NMR, and interaction with cetylpyridinium chloride.

    Science.gov (United States)

    Kogej, Ksenija; Fonseca, Sofia M; Rovisco, José; Azenha, M Emília; Ramos, M Luísa; Seixas de Melo, J Sérgio; Burrows, Hugh D

    2013-11-26

    Complexation of isotactic, syndiotactic, and atactic poly(methacrylic acid), PMA, with trivalent lanthanide ions has been studied in water at a degree of neutralization 0.5. Metal ion binding is shown by quenching of cerium(III) fluorescence, enhancement of Tb(III) luminescence, and lanthanide-induced line broadening in the PMA (1)H NMR spectra. Comparison with lanthanide-acetate complexation suggests carboxylate binds in a bidentate fashion, while Ce(III) luminescence quenching suggests an ≈3:1 carboxylate:metal ion stoichiometry, corresponding to charge neutralization. The presence of both free and bound Ce(III) cations in PMA solutions is confirmed from luminescence decays. Studies of Tb(3+) luminescence lifetime in H2O and D2O solutions show complexation is accompanied by loss of 5-6 water molecules, indicating that each bidentate carboxylate replaces two coordinated water molecules. The behavior depends on pH and polyelectrolyte stereoregularity, and stronger binding is observed with isotactic polyelectrolyte. Binding of cetylpyridinium chloride, CPC, in these systems is studied by luminescence, NMR, and potentiometry. NMR and Tb(3+) luminescence lifetime studies show the strongest binding with the isotactic polymer. Binding of surfactant to poly(methacrylate) in the presence of lanthanides is noncooperative, i.e., it binds to the free sites; binding isotherms in the presence of lanthanides are shifted to higher free surfactant concentrations, compared with sodium ions, have lower slopes and show a clear two-step binding mechanism. While CPC readily replaces the Na(+) ions of poly(methacrylate) and binds very strongly (low critical association concentrations), exchange is much more difficult with the strongly bound trivalent lanthanide ions. Effects of tacticity are seen, with surfactant interacting most strongly with isotactic chains in the initial stages of binding, while in the final stages of binding the interaction is strongest with atactic poly(methacrylate).

  7. 再生混凝土中氯离子渗透性能试验研究%Experimental Study on Chloride Ion Penetration into Recycled Aggregate Concrete

    Institute of Scientific and Technical Information of China (English)

    吴相豪; 岳鹏君

    2011-01-01

    In order to investigate the effects of recycled concrete aggregate, wet and dry cycles, fly ash replacement on chloride ion penetration of recycled aggregate concrete, the chloride ion concentration in recycled aggregate concrete was measured during chloride natural diffusion test. The results show that the a-bility to resist chloride ion penetrate into recycled aggregate concrete is weaker than that for natural aggregate concrete; the resistance to chloride ion penetration into recycled aggregate concrete can be improved by replacing cement with fly ash, 20%(by mass> replacement of cement with fly ash is optimum; the rate . Of chloride ion penetration into recycled aggregate concrete under wet and dry cycles is higher than that into saturated recycled aggregate concrete.%通过氯离子自然扩散试验,测定再生混凝土试件中的氯离子浓度,分析了再生骨料、粉煤灰掺量、全浸泡与干湿循环方式对再生混凝土中氯离子渗透性能的影响.结果表明:再生混凝土抗氯离子渗透能力比普通混凝土差;掺入粉煤灰能提高再生混凝土抗氯离子渗透能力,粉煤灰最佳掺量为20%(质量分数);干湿循环方式可加快再生混凝土中氯离子的渗透速度.

  8. Complexing of niobium (5) ions with benzoylphenylhydroxylamine and lumogallion in the presence of cetylpyridinium chloride

    Energy Technology Data Exchange (ETDEWEB)

    Pilipenko, A.T.; Patratij, Yu.V.; Zul' figarov, O.S. (AN Ukrainskoj SSR, Kiev. Inst. Kolloidnoj Khimii i Khimii Vody; Chernovitskij Meditsinskij Inst. (Ukrainian SSR))

    1985-01-01

    Optimal conditions of formation and extraction by chloroform of different-ligand niobium complex with benzoylphenylhydroxylamine, lumogallion (LG) in the presence of cetylpyridinium chloride (CP) were clarified. It is shown that CP causes transformation of quinonehydrazone into hydroxy-azo-form of the dye by means of interaction with the LG through sulfogroup. It was assumed that CP interaction through hydroxy groups is possible in a different ligand complex. This fact makes conditions for decrease of detection limit and increase of contrast of the reaction of formation of different-ligand niobium complex.

  9. Influence of Blended Cements with Calcareous Fly Ash on Chloride Ion Migration and Carbonation Resistance of Concrete for Durable Structures

    Directory of Open Access Journals (Sweden)

    Michał A. Glinicki

    2016-01-01

    Full Text Available The objective of this paper is to examine the possible use of new blended cements containing calcareous fly ash in structural concrete, potentially adequate for structural elements of nuclear power plants. The investigation included five new cements made with different contents of non-clinker constituents: calcareous fly ash, siliceous fly ash, ground granulated blastfurnace slag, and a reference cement—ordinary Portland cement. The influence of innovative cements on the resistance of concrete to chloride and carbonation exposure was studied. Additionally, an evaluation of the microstructure was performed using optical microscopy on concrete thin sections. Test results revealed a substantial improvement of the resistance to chloride ion penetration into concrete containing blended cements. The resistance was higher for increased clinker replacement levels and increased with curing time. However, concrete made with blended cements exhibited higher depth of carbonation than the Portland cement concrete, except the Portland-fly ash cement with 14.3% of calcareous fly ash. The thin sections analysis confirmed the values of the carbonation depth obtained from the phenolphthalein test. Test results indicate the possible range of application for new cements containing calcareous fly ash.

  10. Cytological comparison of gill chloride cells and blood serum ion concentrations in kutum (Rutilus frisii kutum spawners from brackish (Caspian Sea and fresh water (Khoshkrood River environments

    Directory of Open Access Journals (Sweden)

    Ghahremanzadeh Zahra

    2014-09-01

    Full Text Available The size and number of chloride cells and serum ion concentrations in kutum, Rutillus frisii kutum Nordman, from brackish (Caspian Sea and fresh water (Khoshkrood River environments were studied to gain a better understanding of osmoregulation in this species. Twenty mature kutum specimens were collected from the Caspian Sea (Anzali coasts, 8.49 ppt salinity and 12.4°C temperature and 20 specimens from Khoshkrood River (0.18 ppt salinity and 18°C temperature. Gill samples were analyzed histologically and concentrations of Na+, Cl- , K+, and Mg2+ ions were determined in the blood serum. Concentrations of Na+, Cl- , K+, and Mg2+ ions and osmotic pressure in mature kutum from brackish water were significantly higher than in specimens from fresh water. The average size and number of chloride cells in the fish from seawater were considerably larger than those from fresh water. The mean size of chloride cells was 6.89 ± 1.16 μm in brackish water samples and 5.1 ± 0.81 μm in river samples. The average number of chloride cells in brackish and river water samples were 16.92 and 6.57, respectively. The density and size of chloride cells increased with increases in salinity

  11. Sodium Chloride interaction with solvated and crystalline cellulose : sodium ion affects the tetramer and fibril in aqueous solution

    CERN Document Server

    Bellesia, Giovanni

    2013-01-01

    Inorganic salts are a natural component of biomass which have a significant effect on the product yields from a variety of biomass conversion processes. Understanding their effect on biomass at the microscopic level can help discover their mechanistic role. We present a study of the effect of aqueous sodium chloride (NaCl) on the largest component of biomass, cellulose, focused on the thermodynamic and structural effect of a sodium ion on the cellulose tetramer, and fibril. Replica exchange molecular dynamics simulations of a cellulose tetramer reveal a number of preferred cellulose-Na contacts and bridging positions. Large scale MD simulations on a model cellulose fibril find that Na+ perturbs the hydroxymethyl rotational state population and consequently disrupts the "native" hydrogen bonding network.

  12. Optimisation of the batch reactor for the removal of cobalt ions from chloride media.

    Science.gov (United States)

    Wen Min, Soh; Hasnat, M A; Rahim, Afidah Abd; Mohamed, Norita

    2013-01-01

    A series of experiments were carried out to determine the best medium for the recovery of cobalt by means of an electrogenerative system. Use of the electrogenerative system with a chloride medium had shown promising performance with the highest free energy of -389.8 kJ mol(-1) compared to that with sulphate and nitrate media. Subsequently, the influence of catholyte concentrations on cobalt recovery using the electrogenerative process was carried out by varying the initial cobalt concentration and sodium chloride concentration. The results showed that almost 100% recovery was attained within 1-4 h of the recovery process. Influence of pH was investigated where the electrogenerative system performed best between pH 5.0 and 7.0. Maximum cell performance of 83% with 99% cobalt removal was obtained at 90 min when 100 mg L(-1) of Co(2+) in 0.5 M NaCl was taken as catholyte solution. The values of ΔH(o) and ΔS(o) of the process were evaluated as 33.41 kJ mol(-1) and 0.13 kJ mol(-1), respectively.

  13. Changes in cationic selectivity of the nicotinic channel at the rat ganglionic synapse: a role for chloride ions?

    Directory of Open Access Journals (Sweden)

    Oscar Sacchi

    Full Text Available The permeability of the nicotinic channel (nAChR at the ganglionic synapse has been examined, in the intact rat superior cervical ganglion in vitro, by fitting the Goldman current equation to the synaptic current (EPSC I-V relationship. Subsynaptic nAChRs, activated by neurally-released acetylcholine (ACh, were thus analyzed in an intact environment as natively expressed by the mature sympathetic neuron. Postsynaptic neuron hyperpolarization (from -40 to -90 mV resulted in a change of the synaptic potassium/sodium permeability ratio (P(K/P(Na from 1.40 to 0.92, corresponding to a reversible shift of the apparent acetylcholine equilibrium potential, E(ACh, by about +10 mV. The effect was accompanied by a decrease of the peak synaptic conductance (g(syn and of the EPSC decay time constant. Reduction of [Cl(-](o to 18 mM resulted in a change of P(K/P(Na from 1.57 (control to 2.26, associated with a reversible shift of E(ACh by about -10 mV. Application of 200 nM αBgTx evoked P(K/P(Na and g(syn modifications similar to those observed in reduced [Cl(-](o. The two treatments were overlapping and complementary, as if the same site/mechanism were involved. The difference current before and after chloride reduction or toxin application exhibited a strongly positive equilibrium potential, which could not be explained by the block of a calcium component of the EPSC. Observations under current-clamp conditions suggest that the driving force modification of the EPSC due to P(K/P(Na changes represent an additional powerful integrative mechanism of neuron behavior. A possible role for chloride ions is suggested: the nAChR selectivity was actually reduced by increased chloride gradient (membrane hyperpolarization, while it was increased, moving towards a channel preferentially permeable for potassium, when the chloride gradient was reduced.

  14. Cytoplasmic pathway followed by chloride ions to enter the CFTR channel pore.

    Science.gov (United States)

    El Hiani, Yassine; Negoda, Alexander; Linsdell, Paul

    2016-05-01

    Most ATP-binding cassette (ABC) proteins function as ATP-dependent membrane pumps. One exception is the cystic fibrosis transmembrane conductance regulator (CFTR), an ABC protein that functions as a Cl(-) ion channel. As such, the CFTR protein must form a continuous pathway for the movement of Cl(-) ions from the cytoplasm to the extracellular solution when in its open channel state. Extensive functional investigations have characterized most parts of this Cl(-) permeation pathway. However, one region remains unexplored-the pathway connecting the cytoplasm to the membrane-spanning pore. We used patch clamp recording and extensive substituted cysteine accessibility mutagenesis to identify amino acid side-chains in cytoplasmic regions of CFTR that lie close to the pathway taken by Cl(-) ions as they pass from the cytoplasm through this pathway. Our results suggest that Cl(-) ions enter the permeation pathway via a single lateral tunnel formed by the cytoplasmic parts of the protein, and then follow a fairly direct central pathway towards the membrane-spanning parts of the protein. However, this pathway is not lined continuously by any particular part of the protein; instead, the contributions of different cytoplasmic regions of the protein appear to change as the permeation pathway approaches the membrane, which appears to reflect the ways in which different cytoplasmic regions of the protein are oriented towards its central axis. Our results allow us to define for the first time the complete Cl(-) permeation pathway in CFTR, from the cytoplasm to the extracellular solution.

  15. Identification of a chloride ion binding site in Na+/Cl -dependent transporters.

    Science.gov (United States)

    Forrest, Lucy R; Tavoulari, Sotiria; Zhang, Yuan-Wei; Rudnick, Gary; Honig, Barry

    2007-07-31

    The recent determination of the crystal structure of the leucine transporter from Aquifex aeolicus (aaLeuT) has provided significant insights into the function of neurotransmitter:sodium symporters. Transport by aaLeuT is Cl(-) independent, whereas many neurotransmitter:sodium symporters from higher organisms depend on Cl(-) ions. However, the only Cl(-) ion identified in the aaLeuT structure interacts with nonconserved residues in extracellular loops, and thus the relevance of this binding site is unclear. Here, we use calculations of pK(A)s and homology modeling to predict the location of a functionally important Cl(-) binding site in serotonin transporter and other Cl(-)-dependent transporters. We validate our model through the site-directed mutagenesis of residues predicted to coordinate the Cl(-) ion and through the observation of sequence conservation patterns in other Cl(-)-dependent transporters. The proposed site is located midway across the membrane and is formed by residues from transmembrane helices 2, 6, and 7. It is close to the Na1 sodium binding site, thus providing an explanation for the coupling of Cl(-) and Na(+) ions during transport. Other implications of the model are also discussed.

  16. Solvated Positron Chemistry. The Reaction of Hydrated Positrons with Chloride Ions

    DEFF Research Database (Denmark)

    Mogensen, O. E.; Shantarovich, V. P.

    1974-01-01

    The reaction of hydrated positrons (caq+ with cloride ions in aqueous solutions has been studied by means of positron annihilation angular correlation measurements. A rate constant of k = (2.5 ± 0.5) × 1010 M−1 s−1 was found. Probably the reacting positrons annihilated from an e+ Cl− bound state...

  17. Diffusion of Chloride Ions in Soils: Ⅰ.Influences of Soil Moisture,Bulk Density and Temperature

    Institute of Scientific and Technical Information of China (English)

    XUMINGGANG; ZHANGYIPING; 等

    1997-01-01

    Diffusion coefficients of chlorde ions in four soils of different exture with varying effective moisture content and varying bulk density from 1.1 to 1.6 g cm3 under three different temperatures were determined by the diffusion-cell method using 36Cl-labelled CaCl2 solution.The result showed that activation energy decreased with water content,which indicated that the threshold fro diffusion was lower at a higher soil moisture rate .Therefor,the diffusion coefficient(D) of chloride ions in soil increased consistently with soil moisture,Although a near linear increase in the diffusion coefficient with increasing soil moisture or bulk density in all the soils was observed,the increase rate in different soils was not the same.The D value increased with teperature,and with temperature increased by 10℃ in the range from 5℃to 45℃ the D valve increased by 10%-30%,averaging about 20%.

  18. Simultaneous determination of fluoride, chloride, sulfate, phosphate,monofluorophosphate, glycerophosphate, sorbate, and saccharin in gargles by ion chromatography

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yan-zhen; ZHOU Yan-chun; LIU Li; ZHU Yan

    2007-01-01

    Simple, reliable and sensitive analytical methods to determine anticariogenic agents, preservatives, and artificial sweeteners contained in commercial gargles are necessary for evaluating their effectiveness, safety, and quality. An ion chromatography (IC) method has been described to analyze simultaneously eight anions including fluoride, chloride, sulfate, phosphate,monofluorophosphate, glycerophosphate (anticariogenic agents), sorbate (a preservative), and saccharin (an artificial sweetener)in gargles. In this IC system, we applied a mobile phased gradient elution with KOH, separation by IonPac AS18 columns, and suppressed conductivity detection. Optimized analytical conditions were further evaluated for accuracy. The relative standard deviations (RSDs) of the inter-day's retention time and peak area of all species were less than 0.938% and 8.731%, respectively,while RSDs of 5-day retention time and peak area were less than 1.265% and 8.934%, respectively. The correlation coefficients for targeted analytes ranged from 0.999 7 to 1.000 0. The spiked recoveries for the anions were 90%~102.5%. We concluded that the method can be applied for comprehensive evaluation of commercial gargles.

  19. A comparative study of chelating and cationic ion exchange resins for the removal of palladium(II) complexes from acidic chloride media.

    Science.gov (United States)

    Hubicki, Zbigniew; Wołowicz, Anna

    2009-05-30

    The increasing demand for palladium for technological application requires the development of ion exchange chromatography. Recently ion exchange chromatography has developed largely as a result of new types of ion exchangers available on the market of which two types are widely applied. One of them are selective (chelating) and modified ion exchangers and the other one are liquid exchangers. Two types of ion exchange resins such as chelating (Lewatit TP 214, Purolite S 920) and cationic (Chelite S, Duolite GT 73) ion exchangers are used for the recovery of palladium(II) complexes from chloride media (0.1-2.0M HCl-1.0M NaCl-0.0011 M Pd(II); 0.1-2.0M HCl-2.0M NaCl-0.0011M Pd(II)). The influence of concentration of hydrochloric acid, sodium chloride as well as the phase contact time on the degree of recovery of palladium(II) complexes was studied. Moreover, the amount of palladium(II) chlorocomplexes sorbed onto ion exchangers, the working ion exchange capacities and the weight and bed distribution coefficients were calculated in order to judge which of two types of resins possesses the best performance towards palladium(II) complexes.

  20. Geometric isotope effects on small chloride ion water clusters with path integral molecular dynamics simulations

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Qi [Department of Chemistry, Tsukuba University, 1-1-1 Tennodai, Tsukuba 305-8571 (Japan); Suzuki, Kimichi [Research Institute for Nanosystem, National Institute of Advanced Industrial Science and Technology, Chuo-2, 1-1-1 Umezono, Tsukuba, Ibaraki 305-8568 (Japan); Nagashima, Umpei, E-mail: u.nagashima@aist.go.jp [Department of Chemistry, Tsukuba University, 1-1-1 Tennodai, Tsukuba 305-8571 (Japan); Research Institute for Nanosystem, National Institute of Advanced Industrial Science and Technology, Chuo-2, 1-1-1 Umezono, Tsukuba, Ibaraki 305-8568 (Japan); Tachikawa, Masanori [Quantum Chemistry Division, Graduate School of Science, Yokohama-City University, Seto 22-2, Kanazawa-ku, Yokohama 236-0027 (Japan); Yan, Shiwei [College of Nuclear Science and Technology, Beijing Normal University, Beijing 100875 (China)

    2013-11-29

    Highlights: • PIMD simulations with PM6-DH+ potential are carried out for Cl{sup −}(H{sub 2}O){sub n} clusters. • The geometric isotope effects on the rearrangement of single and multi shell structures are presented. • The competition of intramolecular and intermolecular nuclear quantum effects on the cluster structures is shown. • The correlations between r(Cl…O) and other vibration motions are discussed. - Abstract: The geometric isotope effects on the structures of hydrated chloride ionic hydrogen bonded clusters are explored by carrying out path integral molecular dynamics simulations. First, an outer shell coordinate is selected to display the rearrangement of single and multi hydration shell cluster structures. Next, to show the competition of intramolecular and intermolecular nuclear quantum effects, the intramolecular OH{sup ∗} stretching and intermolecular ion–water wagging motions are studied for single and multi shell structures, respectively. The results indicate that the intermolecular nuclear quantum effects stabilize the ionic hydrogen bonds in single shell structures, while they are destabilized through the competition with intramolecular nuclear quantum effects in multi shell structures. In addition, the correlations between ion–water stretching motion and other cluster vibrational coordinates are discussed. The results indicate that the intermolecular nuclear quantum effects on the cluster structures are strongly related to the cooperation of the water–water hydrogen bond interactions.

  1. Calix[4]arene based dipodal receptor nanohybrids for selective determination of chloride ions in aqueous media.

    Science.gov (United States)

    Kaur, Harpreet; Singh, Jasminder; Chopra, Shweta; Kaur, Navneet

    2016-01-01

    A chemical sensor based on p-tert butyl calix[4]arene has been synthesized and characterized using an assortment of spectroscopic techniques such as (1)H NMR, (13)C NMR, and elemental analysis. For sensor application, organic nanoparticles (N1) of 1 have been primed by implementing re-precipitation technique, which were further employed for preparing organic-inorganic hybrid (H1) by decorating N1 with gold nanoparticles. Both N1 and H1 were characterized using UV-visible, fluorescence, and DLS studies. Photo-physical changes due to anion binding with H1 were scrutinized using UV-visible absorption spectrometer and found it to promptly and selectively recognize Cl(-) ions in aqueous media. Thus, H1 can be effectively used for recognition of Cl(-) ions in aqueous media over a wide pH range, in samples of real time importance with a detection limit of 2.84×10(-9) M with a linear detection range up to 50 μM.

  2. Ion-pair formation in aqueous strontium chloride and strontium hydroxide solutions under hydrothermal conditions by AC conductivity measurements.

    Science.gov (United States)

    Arcis, H; Zimmerman, G H; Tremaine, P R

    2014-09-01

    Frequency-dependent electrical conductivities of solutions of aqueous strontium hydroxide and strontium chloride have been measured from T = 295 K to T = 625 K at p = 20 MPa, over a very wide range of ionic strength (3 × 10(-5) to 0.2 mol kg(-1)), using a high-precision flow AC conductivity instrument. Experimental values for the concentration-dependent equivalent conductivity, Λ, of the two electrolytes were fitted with the Turq-Blum-Bernard-Kunz ("TBBK") ionic conductivity model, to determine ionic association constants, K(A,m). The TBBK fits yielded statistically significant formation constants for the species SrOH(+) and SrCl(+) at all temperatures, and for Sr(OH)2(0) and SrCl2(0) at temperatures above 446 K. The first and second stepwise association constants for the ion pairs followed the order K(A1)(SrOH(+)) > K(A1)(SrCl(+)) > K(A2)[Sr(OH)2(0)] > K(A2)[SrCl2(0)], consistent with long-range solvent polarization effects associated with the lower static dielectric constant and high compressibility of water at elevated temperatures. The stepwise association constants to form SrCl(+) agree with previously reported values for CaCl(+) to within the combined experimental error at high temperatures and, at temperatures below ∼375 K, the values of log10 KA1 for strontium are lower than those for calcium by up to ∼0.3-0.4 units. The association constants for the species SrOH(+) and Sr(OH)2(0) are the first accurate values to be reported for hydroxide ion pairs with any divalent cation under these conditions.

  3. Cytosolic chloride ion is a key factor in lysosomal acidification and function of autophagy in human gastric cancer cell.

    Science.gov (United States)

    Hosogi, Shigekuni; Kusuzaki, Katsuyuki; Inui, Toshio; Wang, Xiangdong; Marunaka, Yoshinori

    2014-06-01

    The purpose of the present study was to clarify roles of cytosolic chloride ion (Cl(-) ) in regulation of lysosomal acidification [intra-lysosomal pH (pHlys )] and autophagy function in human gastric cancer cell line (MKN28). The MKN28 cells cultured under a low Cl(-) condition elevated pHlys and reduced the intra-lysosomal Cl(-) concentration ([Cl(-) ]lys ) via reduction of cytosolic Cl(-) concentration ([Cl(-) ]c ), showing abnormal accumulation of LC3II and p62 participating in autophagy function (dysfunction of autophagy) accompanied by inhibition of cell proliferation via G0 /G1 arrest without induction of apoptosis. We also studied effects of direct modification of H(+) transport on lysosomal acidification and autophagy. Application of bafilomycin A1 (an inhibitor of V-type H(+) -ATPase) or ethyl isopropyl amiloride [EIPA; an inhibitor of Na(+) /H(+) exchanger (NHE)] elevated pHlys and decreased [Cl(-) ]lys associated with inhibition of cell proliferation via induction of G0 /G1 arrest similar to the culture under a low Cl(-) condition. However, unlike low Cl(-) condition, application of the compound, bafilomycin A1 or EIPA, induced apoptosis associated with increases in caspase 3 and 9 without large reduction in [Cl(-) ]c compared with low Cl(-) condition. These observations suggest that the lowered [Cl(-) ]c primarily causes dysfunction of autophagy without apoptosis via dysfunction of lysosome induced by disturbance of intra-lysosomal acidification. This is the first study showing that cytosolic Cl(-) is a key factor of lysosome acidification and autophagy.

  4. Kinetic and equilibrium studies of the removal of cadmium ions from acidic chloride solutions by hydrophobic pyridinecarboxamide extractants

    Energy Technology Data Exchange (ETDEWEB)

    Borowiak-Resterna, Aleksandra [Institute of Chemical Technology and Engineering, Poznan University of Technology, Pl. Marii Sklodowskiej-Curie 2, 60-965 Poznan (Poland); Cierpiszewski, Ryszard [Poznan University of Economics, Faculty of Commodity Science, al. Niepodleglosci 10, 61-875 Poznan (Poland); Prochaska, Krystyna, E-mail: Krystyna.Prochaska@put.poznan.pl [Institute of Chemical Technology and Engineering, Poznan University of Technology, Pl. Marii Sklodowskiej-Curie 2, 60-965 Poznan (Poland)

    2010-07-15

    Liquid-liquid extraction of cadmium(II) from acidic chloride solutions was carried out with alkyl derivatives of pyridinecarboxamide in toluene with addition of 2-ethylhexan-1-ol as modifier. Equilibrium as well as kinetic studies was performed. The kinetic studies of a Cd(II) extraction process were carried out with a Lewis cell having a constant interfacial area. Cadmium(II) concentration in the aqueous phases was determined by atomic absorption spectroscopy (Varian SPECTR AA800). The results of equilibrium experiments showed that cadmium(II) was quantitatively extracted with N,N-dihexylpyridine-3-carboxamide whereas the derivative N,N-dihexylpyridine-2-carboxamide was not able to transfer Cd(II) ions from the aqueous phase to the organic one. Thus, the kinetics of extraction and the initial extraction rate were examined only in the systems with N,N-dihexylpyridine-3-carboxamide. The obtained experimental data as well as the calculated values of mass transfer coefficients suggest that the investigated process of extraction of Cd(II) by means of pyridinecarboxamide as extractant occurs in the mixed diffusion-kinetic region. Moreover, the results of adsorption studies indicated that the extraction of Cd(II) with a hydrophobic extractant should be considered as an interfacial process.

  5. Effect of Chloride ion and Zirconium hydride on thr corrosion and SCC behaviors of functionally graded Zirconium alloy p.683

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Y. [Department of Metallurgical and Materials Engineering, Sunmoon University, Asam (Korea, Republic of); Kim, B. G.; Lee, J. W.; Kang, Y. H. [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

    2000-07-01

    Effect of chloride ion and zirconium hydride on the corrosion and stress corrosion cracking behaviors of functionally graded zirconium alloy was studied to develop an advanced nuclear cladding tubing. The functionally graded zirconium alloy had composition gradient of niobium, which was prepared with a hot pressing followed by cold deformation. The corrosion rates and potentials decreased with increasing FeCl{sub 3} and hydride content. The corrosion potentials before and after hydriding are -4.3 V{sub SHE}, 8.8x10{sup -5} A{sub cm}{sup -2} and -12.5 V{sub SHE}, 3.9x10{sup -4} A{sub cm}{sup -2}, respectively. The stress corrosion cracking susceptibility decreased with elongation rate, indicating the saturation value at 5x10{sup -7} sec{sup -1}. SEM observation showed that brittle fracture with corrosion products and pits were observed on the failed surface of hydrided zirconium alloy, suggesting anodic dissolution occurred during exposure after cracking growth along zirconium hydrides. (author)

  6. Chloride ions promoted the catalytic wet peroxide oxidation of phenol over clay-based catalysts.

    Science.gov (United States)

    Zhou, Shiwei; Zhang, Changbo; Xu, Rui; Gu, Chuantao; Song, Zhengguo; Xu, Minggang

    2016-01-01

    Catalytic wet peroxide oxidation (CWPO) of phenol over clay-based catalysts in the presence and absence of NaCl was investigated. Changes in the H2O2, Cl(-), and dissolved metal ion concentration, as well as solution pH during phenol oxidation, were also studied. Additionally, the intermediates formed during phenol oxidation were detected by liquid chromatography-mass spectroscopy and the chemical bonding information of the catalyst surfaces was analyzed by X-ray photoelectron spectroscopy (XPS). The results showed that the presence of Cl(-) increased the oxidation rate of phenol to 155%, and this phenomenon was ubiquitous during the oxidation of phenolic compounds by H2O2 over clay-based catalysts. Cl(-)-assisted oxidation of phenol was evidenced by several analytical techniques such as mass spectroscopy (MS) and XPS, and it was hypothesized that the rate-limiting step was accelerated in the presence of Cl(-). Based on the results of this study, the CWPO technology appears to be promising for applications in actual saline phenolic wastewater treatment.

  7. Why are ionic liquid ions mainly associated in water? A Car-Parrinello study of 1-ethyl-3-methyl-imidazolium chloride water mixture

    Science.gov (United States)

    Spickermann, C.; Thar, J.; Lehmann, S. B. C.; Zahn, S.; Hunger, J.; Buchner, R.; Hunt, P. A.; Welton, T.; Kirchner, B.

    2008-09-01

    In this study we present the results of a first principles molecular dynamics simulation of a single 1-ethyl-3-methyl-imidazolium chloride [C2C1im][Cl] ion pair dissolved in 60 water molecules. We observe a preference of the in plane chloride coordination with respect to the cation ring plane as compared to the energetic slightly more demanding on top coordination. Evaluation of the different radial distribution functions demonstrates that the structure of the hydration shell around the ion pair differs significantly from bulk water and that no true ion pair dissociation in terms of completely autonomous solvation shells takes place on the timescale of the simulation. In addition, dipole moment distributions of the solvent in distinct solvation shells around different functional parts of the [C2C1im][Cl] ion pair are calculated from maximally localized Wannier functions. The analysis of these distributions gives evidence for a depolarization of water molecules close to the hydrophobic parts of the cation as well as close to the anion. Examination of the angular distribution of different OH(H2O )-X angles in turn shows a linear coordination of chloride accompanied by a tangential orientation of water molecules around the hydrophobic groups, being a typical feature of hydrophobic hydration. Based on these orientational aspects, a structural model for the obvious preference of ion pair association is developed, which justifies the associating behavior of solvated [C2C1im][Cl] ions in terms of an energetically favorable interface between the solvation shells of the anion and the hydrophobic parts of the cation.

  8. Removal of copper (II) from aqueous solutions by flotation using polyaluminum chloride silicate (PAX-XL60 S) as coagulant and carbonate ion as activator.

    Science.gov (United States)

    Ghazy, S E; Mahmoud, I A; Ragab, A H

    2006-01-01

    Flotation is a separation technology for removing toxic heavy metal ions from aqueous solutions. Here a simple and rapid flotation procedure is presented for the removal of copper(II) from aqueous solutions. It is based on the use of polyaluminum chloride silicate (PAX-XL60 S) as coagulant and flocculent, carbonate ion as activator and oleic acid (HOL) as surfactant. Both ion and precipitate flotation are included depending on the solution pH. Ion and precipitate flotation in the aqueous HOL-PAX-XL60 S-Cu2+-CO3(2-) system gave powerful preferential removal of Cu2+ (F -100%) over the HOL-PAX-XL60 S-Cu2+ system containing no CO3(2+) ion (F approximately 86%). The role of CO3(2-) ion is also evident from decreasing the dose of PAX-XL60 S from 700 mg l(-1) to 200 mg l(-1). The other parameters, influencing the flotation process, namely: metal ion, surfactant and PAX-XL60 S concentrations, ionic strength, temperature and foreign ions were examined. Moreover, the procedure was successfully applied to recover Cu2+ ions from different volumes up to 11 and from natural water samples.

  9. Ion-pair hollow-fiber liquid-phase microextraction of the quaternary ammonium surfactant dicocodimethylammonium chloride.

    Science.gov (United States)

    Hultgren, Sofie; Larsson, Niklas; Nilsson, Bo F; Jönsson, Jan Ake

    2009-02-01

    A two-phase hollow-fiber (HF) liquid-phase microextraction (LPME) method was developed for determination of a quaternary ammonium compound surfactant, dicocodimethylammonium chloride, in aqueous samples. The porous HF was fixed on a metal rod support and was impregnated with approximately 6.6 microL of organic extractant, which was immobilized in the HF pores. Surfactant extraction was facilitated by addition of carboxylic acid to the sample forming neutral ion pairs with the quaternary ammonium compound. After extraction, the analyte was transferred from the organic extractant in the fiber pores by dissolving the 1-octanol into 100 microL methanol. The methanol extract was analyzed by liquid chromatography-mass spectrometry. The method was optimized (with optimized parameters in brackets) with regard to type of organic extractant (1-octanol), fiber length (2 cm), choice and concentration of anionic carrier (600 microg L(-1) octanoate), procedure of transfer to methanol (15-min sonication), sample volume (250 mL), extraction time (17 h), pH (10), and ionic strength (50 mM carbonate). Aspects influencing repeatability in LPME of (quaternary ammonium) surfactants are discussed. The enrichment factor achieved in 250-mL carbonate buffer was around 400. Due to matrix effects, the enrichment factors achieved when industrial process water was analyzed were 120 or about 30% of that in carbonate buffer. Detection limits of 0.3 microg L(-1) in carbonate buffer and 0.9 microg L(-1) in industrial process water were obtained. If the studied compound is seen as a model substance representing quaternary dialkylated dimethylated ammonium surfactants in general, the developed method may be applied to other quaternary ammonium surfactants.

  10. Zn–Al layered double hydroxides intercalated with carbonate, nitrate, chloride and sulphate ions: Synthesis, characterisation and dye removal properties

    Directory of Open Access Journals (Sweden)

    Fatima Zahra Mahjoubi

    2017-01-01

    Full Text Available In this work, Zn–Al layered double hydroxides intercalated with carbonate, nitrate, chloride and sulphate ions were synthesised via a co-precipitation method at a constant solution pH. The as-synthesised samples were characterised by X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, transmission electron microscopy (TEM and simultaneous thermogravimetric/differential thermal analysis (TGA-DTA. The XRD patterns showed that Zn-Al-SO4 had the greatest interlayer spacing, followed by Zn-Al-Cl, Zn-Al-NO3 and Zn-Al-CO3. The FTIR spectra clearly confirmed the presence of intercalated anions in the structure of the LDHs. Batch experiments for methyl orange (MO adsorption onto synthesised samples were investigated under various conditions such as contact time, initial dye concentration and solution pH. The experimental results show that pH is the most influencing factor. The effective pH range for the MO removal was found to be 3.5–4.5. The kinetics data can be described accurately by a pseudo-second-order kinetic model instead of a pseudo-first-order model. The equilibrium data were analysed using the Langmuir, Freundlich and Dubinin–Radushkevich models. The results showed that the Langmuir and Dubinin–Radushkevich isotherm models fit well to the experimental data. The Zn-Al-LDH samples exhibited exceptional Langmuir maximum adsorption capacities of 2758, 2455, 2270 and 1684 mg/g for Zn-Al-SO4, Zn-Al-Cl, Zn-Al-NO3 and Zn-Al-CO3, respectively.

  11. Role of Chloride Ion and Dissolved Oxygen in Electrochemical Corrosion of AA5083-H321 Aluminum-Magnesium Alloy in NaCl Solutions under Flow Conditions

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Flow-induced corrosion consists electrochemical and mechanical components. The present paper has to assessed the role of chloride ion and dissolved oxygen in the electrochemical component of flow induced corrosion for AA5083-H321 aluminum-magnesium alloy which is extensively used in the construction of high-speed boats, submarines, hovercrafts, and desalination systems, in NaCl solutions. Electrochemical tests were carried out at flow velocities of 0, 2, 5, 7 and 10 m/s, in aerated and deaerated NaCl solutions with different sodium chloride concentrations. The results showed that the high rate of oxygen reduction under hydrodynamic conditions causes an increase in the density of pits on the surface. The increase of chloride ions concentration under flow conditions accelerates the rate of anodic reactions, but have no influence on the cathodic reactions. Thus, in the current work, it was found that under flow conditions, due to the elimination of corrosion products inside the pits, corrosion resistance of the alloy is increased.

  12. 氯化银浊度法测定铜电解液中氯离子%Determination of Chlorine Ion in Copper Electrolyte Using Chloride Turbidimetric Method

    Institute of Scientific and Technical Information of China (English)

    巫来富

    2012-01-01

    在丙酮存在的条件下,铜电解液中的氯离子与硝酸银反应,形成氯化银乳浊液,用铜电解液的原液(即实验中铜电解液原液没有加硝酸银的试液)作参比,于分光光度计500nm处测定其吸光度,从而得出铜电解液中氯离子的含量.%In the condition of Acetone existence,Chloride ion in Copper electrolyte reacted with Silver nitrate,forming the Silver Chloride emulsion.And then we used the initial copper electrolyte solution(i.e.,copper electrolyte solution without the addition of silver nitrate solution) as reference to determine its absorbance at 500nm in spectrophotometer.Finally,we got the content of Chloride ion in Copper electrolyte.

  13. SN2 and SN2' reaction dynamics of cyclopropenyl chloride with halide ion : A direct ab initio molecular dynamics (MD) study

    OpenAIRE

    Tachikawa, Hiroto

    2005-01-01

    Direct ab initio molecular dynamics (MD) calculations have been carried out for the reaction of cyclopropenyl chloride with halide ion (F–) (F– + (CH)3Cl → F(CH)3 + Cl–) in gas phase. Both SN2 and SN2′ channels were found as product channels. These channels are strongly dependent on the collision angle of F– to the target (CH)3Cl molecule. The collision at one of the carbon atoms of the C=C double bond leads to the SN2′ reaction channel; whereas the collision at the methylene carbon atom lead...

  14. Quick Determination of Chloride Ion in Titanium Sponge by Polarography Method%极谱法快速测定海绵钛中的氯离子

    Institute of Scientific and Technical Information of China (English)

    惠秋红; 崔庆雄; 刘坤兰; 毛禹平

    2013-01-01

    提出了用极谱法测定海绵钛中氯离子的新方法.所拟方法较现行比浊法快速简便,体系抗干扰能力虽,节约试剂,与传统方法比对,结果较好.%The new method for determination of chloride ion in titanium sponge by polarograph is presented in this paper. The proposed method compared with the current turbidimetry is rapid, simple and reagent saving; the antijamming capability of the system is strong, and the result is better compared with traditional methods.

  15. Effect of Glass Powder on Chloride Ion Transport and Alkali-aggregate Reaction Expansion of Lightweight Aggregate Concrete

    Institute of Scientific and Technical Information of China (English)

    WANG Zhi; SHI Caijun; SONG Jianming

    2009-01-01

    The effects of glass powder on the strength development, chloride permeability and potential alkali-aggregate reaction expansion of lightweight aggregate concrete were investigated.Ground blast furnace slag, coal fly ash and silica fume were used as reference materials. The re-placement of cement with 25% glass powder slightly decreases the strengthes at 7 and 28 d, but shows no effect on 90 d's. Silica fume is very effective in improving both the strength and chloride penetra-tion resistance, while ground glass powder is much more effective than blast furnace slag and fly ash in improving chloride penetration resistance of the concrete. When expanded shale or clay is used as coarse aggregate, the concrete containing glass powder does not exhibit deleterious expansion even if alkali-reactive sand is used as fine aggregate of the concrete.

  16. 离子色谱法检测食品添加剂焦碳酸二甲酯中的氯离子%Determination of Chloride Ion in Dimethyl Dicarbonate as Food Additives by Ion Chromatography

    Institute of Scientific and Technical Information of China (English)

    张锦梅; 王敬花; 张习志

    2012-01-01

    A method was established for the determination of chloride ion in DMDC (dimethyl dicarbonate ) as food additives by ion exchange chromatography. Sample was separated on SH-AC-1 ( 250 mm x 4.6 mm,5μm ) anion exchange column with suppressed conductivity after being dissluted by water. The effects of the types of eluent, concentration on separation of chloride ion and interfering ion were investigated. The optimized chromatographic conditions were as follows : 0.005 mol/L of sodium borate solution as eluent with flow rate of 1.0 mL/min. On these conditions, the chloride ions and other interfering ions in the sample could be completely separated . The resolution of peak attained 3.0 and the symmetry of peaks was better. The good linear calibration curve were obtained in the chloride ion concentration range of 0.1-5.0 mg / L with the linear relative coefficient more than 0.999. Chloride ion detection limit (S/N=3) was 0.007 mg/L, and the standard added recovery was 97.5%-98.9%. The method is suitable for determination of chloride ions in DMDC as food additives.%建立离子色谱法检测食品添加剂焦碳酸二甲酯( DMDC)中的杂质氯离子的方法.样品用水溶解超声定容后,采用SH-AC-1阴离子交换柱(250 mm×4.6 mm,5 μm)分离,抑制电导法检测.考察了淋洗液种类、浓度对氯离子与干扰离子分离度的影响.最佳色谱条件:以0.005 mol/L的四硼酸钠水溶液为淋洗液,流速1.0 mL/min. 在此条件下,样品中的氯离子可以和其它干扰离子分离,而且分离度迭3.0以上,峰形对称.在氯离子浓度为0.1~5.0mg/L的范围内,可获得良好的线性关系,线性相关系数大于0.999;氯离子检出限(S/ N=3)达0.007 mg/L,加标回收率为97.5%~98.9%.该方法可以用于食品添加剂DMDC中氯离子的测定.

  17. 铜粉处理酸性镀铜溶液中氯离子的机理%Mechanism of Treating Chloride Ion in Acidic Copper Plating Bath with Copper Powder

    Institute of Scientific and Technical Information of China (English)

    郭崇武

    2011-01-01

    阐明了用铜粉处理酸性镀铜溶液中氯离子的机理,理论分析和实验表明,在酸性镀铜溶液中,Cu2+离子与铜粉反应生成Cu+离子,同时氯离子与Cu+离子反应生成氯化亚铜沉淀.向镀液中加铜粉1g/L,氯离子的起始质量浓度为174mg/L时,氯离子的去除率为58.9%,而向镀液中加锌粉1g/L,氯离子的去除率为47.0%,用铜粉处理氯离子的效率较高.%The mechanism of treating chloride ion in acidic copper plating bath by using copper powder was illustrated. Theoretical analyses and experimental tests indicated that in acidic copper plating solution Cu2+ ion could react with copper powder to form Cu + ion and the Cu + ion could react with chloride ion in the solution to produce cuprous chloride precipitation. When the initial mass concentration of the chloride ions in the acidic copper plating solution was 174 mg/L, the elimination rate of chloride ions after adding 1 g/L copper powders to the solution was 58.9% while that after adding 1 g/L zinc powders was 47.0%. This indicates that the treatment efficiency of chloride ion in the acidic copper plating solution with copper powders is higher than that with zinc powders.

  18. Adsorption of Rh(III) complexes from chloride solutions obtained by leaching chlorinated spent automotive catalysts on ion-exchange resin Diaion WA21J

    Energy Technology Data Exchange (ETDEWEB)

    Shen Shaobo, E-mail: shaoboshen@metall.ustb.edu.cn [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China); Department of Physical Chemistry, School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Pan Tonglin; Liu Xinqiang; Yuan Lei [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China); Wang Jinchao [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China); Department of Physical Chemistry, School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Zhang Yongjian; Guo Zhanchen [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China)

    2010-07-15

    It was found that Rh, Pd and Pt contained in the spent ceramic automotive catalysts could be effectively extracted by dry chlorination with chlorine. In order to concentrate Rh(III) ions contained in the chloride solutions obtained, thermodynamic and kinetics studies for adsorption of Rh(III) complexes from the chloride solutions on an anionic exchange resin Diaion WA21J were carried out. Rh, Pd, Pt, Al, Fe, Si, Zn and Pb from the chloride solution could be adsorbed on the resin. The distribution coefficients (K{sub d}) of Rh(III) decreased with the increase in initial Rh(III) concentration or in adsorption temperature. The isothermal adsorption of Rh(III) was found to fit Langmuir, Freundlich and Dubinin-Kaganer-Radushkevich models under the adsorption conditions. The maximum monolayer adsorption capacities Q{sub max} based on Langmuir adsorption isotherms were 6.39, 6.61 and 5.81 mg/g for temperatures 18, 28 and 40 deg. C, respectively. The apparent adsorption energy of Rh was about -7.6 kJ/mol and thus Rh(III) adsorption was a physical type. The experimental data obtained could be better simulated by pseudo-first-order kinetic model and the activation energy obtained was 6.54 J/mol. The adsorption rate of Rh(III) was controlled by intraparticle diffusion in most of time of adsorption process.

  19. Solvent extraction-separation of La(III), Eu(III) and Er(III) ions from aqueous chloride medium using carbamoyl-carboxylic acid extractants

    Institute of Scientific and Technical Information of China (English)

    Reyhaneh Safarbali; Mohammad Reza Yaftian; Abbasali Zamani

    2016-01-01

    N,N-dibutyldiglycol amic acid (HLI) and N,N-dioctyldiglycol amic acid (HLI) were synthesized and characterized by con-ventional spectroscopic methods. These molecules were examined as extractants for extraction-separation of La(III), Eu(III) and Er(III), as representative ions of light, middle and heavy rare earths, from aqueous chloride solutions. The analysis of the extraction equilibria revealed that the extracted species of lanthanum and europium ions by both of the extractants had a 1:3 metal to ligand ratio. It was suggested that erbium ions were extracted into the organic phase via the formation of Er(LI or I)2Cl complexes. The effect of the organic diluents on the extraction-separation efficiency of the studied rare earths by HLI and HLI was investigated by comparing the results obtained in dichloromethane and carbon tetrachloride. Regardless to the diluent used, the order of selectivity presented by the investigated extractants was Er(III)>Eu(III)>La(III). It is noteworthy that, a significant enhancement in separation of the studied rare earths by the extractants was achieved in their competitive extraction experiments with respect to that obtained in single component extraction experiments. Applicability of the extractants for the removal of rare earth ions from spent Ni-MH batteries was tested by removal of La(III), Eu(III) and Er(III) ions from simulated leach solution of such batteries.

  20. Determination of chloride ion in dimethyl dicarbonate as food additives by ion exchange chromatography%离子色谱法检测食品添加剂焦碳酸二甲酯中的氯离子

    Institute of Scientific and Technical Information of China (English)

    张锦梅; 王敬花; 张习志

    2012-01-01

    目的:建立离子色谱法检测食品添加剂焦碳酸二甲酯(DMDC)中的杂质氯离子。方法:样品用水溶解超声定容后,采用SH-AC-1阴离子交换柱(25 cm×4.6 mm,7μm)分离,抑制电导法检测。分别选用碳酸钠,四硼酸钠为淋洗液。考察了淋洗液种类,浓度对氯离子与干扰离子的分离度的影响。最佳色谱条件为:采用0.005 mol/L的四硼酸钠水溶液作为淋洗液,流速1.0 mL/min。结果:在此条件下,样品中的氯离子可以和其他的干扰离子分离,而且分离度达3.0以上,峰形对称。在(0.1~ 5.0 mg/L)范围内,可获得良好的线性关系,线性相关系数大于0.999;氯离子检出限(S/N=3)达(0.007 mg/L),加标回收率达97.5%以上,重现性好。结论:该方法简便快速灵敏准确,可以用于食品添加剂DMDC中氯离子测定。%Objiective: To establish a method for the determination of chloride ion in DMDC (dimethyl dicarbonate) as food additives by ion exchange chromatography. Method: Sample was dissluted by water after ultrasonic, chromatographic separation was performed on a SH-AC-1 (25 cm×4.6 mm, 5μm) anion exchange column, Suppressed conductivity detection. Using sodium carbonate, sodium borate as the eluent, respectively. The effects of the types of eluent, eluent concentration on separation of chloride ion and interfering ion were investigated. The optimized chromatographic conditions for the determination of the chloride were as follows: 0.005 mol/L of sodium borate solution as eluent and flow rate of 1.0 mL/min. Results: Under these conditions, the chloride ions and other interfering ion can be completely separated in the sample, the resolution of peak attained 3.0 or more and the symmetry of peaks was better. The good linear calibration curve were obtained for the range of 0.1-5.0 mg/L with the linear relative coefficient more than 0.999, chloride ion detection limit(SIN:3) was 0.007 mg/L, The

  1. 煤矸石混凝土抗氯离子渗透实验研究%Experiment Study on Chloride Ion Penetration of Coal Gangue Concrete

    Institute of Scientific and Technical Information of China (English)

    李永靖; 邢洋

    2016-01-01

    为了解煤矸石混凝土抗氯离子渗透性能,以自燃煤矸石为粗、细集料,42.5普通硅酸盐水泥为胶凝材料并掺入粉煤灰,制备煤矸石混凝土试件,进行抗氯离子渗透实验,研究了水胶比、粉煤灰掺量以及抗压强度对煤矸石混凝土抗氯离子渗透性能的影响。结果表明:非稳态条件下煤矸石混凝土氯离子渗透深度随水胶比增加而加深,呈正相关,氯离子渗透深度增长速度在水胶比0.42~0.48时较快,在水胶比0.48~0.56时缓慢;氯离子迁移系数与水胶比呈正相关,与粉煤灰掺量呈负相关;氯离子迁移系数随抗压强度增大而减小,呈负相关,负相关显著性强弱表现为粉煤灰掺量0%<粉煤灰掺量20%<粉煤灰掺量40%。掺入粉煤灰可以改善煤矸石混凝土耐久性能。%Take spontaneous combustion coal gangue, 42.5 ordinary portland cement and lfy ash to make coal gangue lightweight aggregate concrete which in order to understand the anti chloride ion permeability. The chloride ion penetration test is carried out that in order to study the relationship between anti chloride ion permeability and water cement ratio, lfy ash content as well as compressive strength. Experimental results show:the chloride ion penetration depth under the condition of non steady state increases with the water cement ratio and is positive correlation. The growth rate is faster between 0.42~0.48 of water cement ratio and slower between 0.48~0.56 of water cement ratio. Chloride migration coefifcient and water cement ratio is positively correlated. Chloride migration coefifcient decreases with the increase of compressive strength and is negative correlation. The strength of the situation is as follows: the lfy ash content of 0% is less than the lfy ash content of 20% and the lfy ash content of 20% is less than the lfy ash content of 40%. Fly ash can improve the durability of coal gangue concrete.

  2. Solvent extraction of the ion-pairs of chromium(VI) and molybdenum(VI) with trioctylmethylammonium chloride and benzyldimethylcetylammonium chloride.

    Science.gov (United States)

    Ohashi, K; Shikina, K; Nagatsu, H; Ito, I; Yamamoto, K

    1984-11-01

    The number of capriquat molecules per chromium(VI) atom in the chromate-capriquat ion-association complex has been found to be between one and two. The distribution ratio in the extraction of chromium(VI) with capriquat is dependent on the dielectric constant of the organic solvent, with a minimum at a dielectric constant of about 8. The absorption spectra of the ion-pair extracted into cyclohexane, carbon tetrachloride, benzene and n-butanol are very similar to that of chromate in aqueous solution. The absorption spectra of the chromium(VI)-capriquat extracts in these organic solvents gradually change to an absorption spectrum similar to that of HCrO(4)(-) in aqueous solution. Chromium(VI)-capriquat extracted into chloroform and 1,2-dichloroethane gives absorption spectra similar to that of HCrO(4)(-)in aqueous medium. The chromium(VI)-capriquat species extracted into 1,2-dichloroethane may be (Q(+))(2).CrO(4)(2-)(H(2)O)(n). In contrast, chromium(VI) is extracted with capriquat into the other organic solvents from ammoniacal medium as a mixture of (Q(+))(2).CrO(4)(2-)(H(2)O)(n) and Q(+).NH(4)(+).CrO(4)(2-)(H(2)O)(n). The spectral change is ascribed to the change of the extracted species from (Q(+))(2).CrO(4)(2-)(H(2)O)(n) and Q(+)NH(4)(+).CrO(4)(-)(H(2)O)(n) to Q(+).HCrO(4)(2-)(H(2)O)(n-1). The chromium(VI)-zephiramine species extracted is formulated as (Q(+), NH(4)(+))(2)CrO(4)(2-)(H(2)O)(n).(Q(+).Cl(-))(m). Molybdenum(VI) is extracted with capriquat into the same organic solvents as a mixture of (Q(+))(2).MoO(4)(2-)(H(2)O)(n) and Q(+).NH(4)(+).MoO(4)(2-).(H(2)O)(n).

  3. Automatic Potentiometric Titrator Determinated Chloride Ions in Water%自动电位滴定仪测定水中氯离子的探讨

    Institute of Scientific and Technical Information of China (English)

    李芳; 李文胜

    2014-01-01

    Using automatic potentiometric titrator, standard solution of silver nitrate was calibrated and chloride ions in industrial circulating wate was determined. The matters need attention of the electrode maintenance and the end point of titration to set were summarized. The result showed that the determination of chloride ions in water by using the instrument, its accuracy and precision can be obtained satisfactory results.%通过使用自动电位滴定仪标定硝酸银标准溶液和测定工业循环水中氯离子的实验研究,总结了在使用中应注意的电极的维护保养和滴定终点设定方面的一些规律,结果表明用该仪器测定水中氯离子,其准确性和精密度均可获得满意的结果。

  4. Determination of the extractive capacity of para-tert butyl calix[8]arene octa-phosphinoylated towards uranyl ions from an aqueous-acidic-salty medium; Determinacion de la capacidad extractiva del p-ter-butilocalix[8]areno octa-fosfinoilado hacia iones uranilo de un medio acuo-acido salino

    Energy Technology Data Exchange (ETDEWEB)

    Serrano V, E. C.

    2011-07-01

    The extraction properties of octa-phosphinoylated para-tert butyl calix[8]arene (prepared in the laboratory) in chloroform towards uranyl ions from an aqueous-acidic-salty medium (HNO{sub 3}-3.5 NaNO{sub 3}) containing uranyl nitrate salt, was investigated. Two spectroscopic techniques UV/Vis and Luminescence were used for this study. The latter permitted analyze the fluorescence from the uranyl ions influenced by the surrounding medium. Both permitted to learn about the power of this calixarene as extractant towards the mentioned ions. Its extraction ability or capability using this calixarene at 5.91 x 10{sup -4} M towards the uranyl ions was 400% as determined by UV/Vis while fluorescence revealed 100% of uranyl ion extraction. A closed analysis of the results obtained by using these techniques revealed that the stoichiometry of the main extracted species was 1calixarene:2 uranyl ions. The loading capacity of the calixarene ligand towards the uranyl ions was also investigated using both techniques. UV/Vis resulted to be inadequate for quantifying exactly the loading capacity of the calixarene whereas luminescence was excellent indeed, using a 5.91 x 10{sup -4} M calixarene concentration, its loading capacity was 0.157 M of free uranyl ions from 0.161 M of uranyl ions present in the aqueous-acidic-salty medium. The extracts from the ability and capacity studies were concentrated to dryness, purified and the dried extracts were analyzed by infrared and neutron activation analysis. By these techniques it was demonstrated that during the extraction of the uranyl ions by the calixarene ligand they form thermodynamically and kinetically stable complexes, since in the solid state, the 1:2, calixarene; uranyl ions stoichiometry was kept with the minimum formula: (UO{sub 2}){sub 2}B{sub 8}bL{sup 8}(NO{sub 3}){sub 4}(H{sub 2}O){sub 4}CHCl{sub 3}(CH{sub 3}OH){sub 3} the methanol molecules come from its purification. It is proposed that B{sub 8}bL{sup 8} calixarene in

  5. 地下水中SO42-和Cl-对Fe0降解TCE的效应研究%Effect of Sulfate and Chloride Ion in Groundwater on TCE Degradation by ZVI-PRB

    Institute of Scientific and Technical Information of China (English)

    张晓庆; 朱雪强; 卜丹阳; 许映军; 陈强

    2011-01-01

    文章基于渗透反应墙技术,通过实验室柱实验分析不同浓度的SO42-和Cl-单独作用下Fe0降解TCE的效果.结果表明:在相同Fe0条件下,随SO42-浓度增大,出水口TCE去除率提高,且SO42-在TCE降解反应中由抑制作用逐渐转换为促进作用;此外随Cl-浓度增大,出水口TCE去除率呈下降趋势,且Cl-在TCE降解反应中由促进作用逐渐转变为抑制作用;同时研究结果表明,Fe0反应柱对Cl-具有一定吸附作用.%Column experiments were done to determine effects of sulfate and chloride ion on TCE degradation by ZVI-PRB. Results showed that sulfate and chloride ion had a dual effect on TCE degradation in the system of ZVI-PRB. As sulfate concentration increased, the efficiency of TCE degradation got better. Sulfate could inhibit the reaction when its concentration was low, however, when its concentration increased, sulfate had a promoting action to the reaction. As chloride ion concentration increased, the efficiency of TCE degradation became worse. When there was a low concentration, chloride ion had a promoting action to the reaction, and when its concentration increased, chloride ion could inhibit the reaction. The study showed that the experiment column can adsorb chloride ion.

  6. Progress of Carbonation in Chloride Contaminated Concretes

    OpenAIRE

    Wang, Yaocheng; Basheer, P. A.M.; Nanukuttan, S; Bai, Y.

    2016-01-01

    Concretes used in marine environment are generally under the cyclic effect of CO2 and chloride ions (Cl-). To date, the influence of carbonation on ingress of chloride ions in concretes has been widely studied; in comparison, study on the influence of Cl- on the progress of carbonation is limited. During the study, concretes were exposed to independent and combined mechanisms of carbonation and chloride ingress regimes. Profiles of apparent pH and chloride concentration were used to indicate ...

  7. New Data on Activity Coefficients of Potassium, Nitrate, and Chloride Ions in Aqueous Solutions of KNO3 and KCl by Ion Selective Electrodes

    OpenAIRE

    Debasmita Dash; Shekhar Kumar; C. Mallika; U. Kamachi Mudali

    2012-01-01

    Ion selective electrodes (ISEs) are used to measure the single-ion activity coefficients in aqueous solutions of KNO3 and KCl at 298.15 K against a double-junction reference electrode. The EMF responses of ISEs up to 0.01 m are plotted to obtain the slope and intercept values. The obtained slopes and intercepts are used in Nernst equation for higher concentrated solutions for calculation of individual ion activity coefficient. The mean ionic activity coefficients are estimated from single ion...

  8. Accelerated solvent extraction followed by on-line solid-phase extraction coupled to ion trap LC/MS/MS for analysis of benzalkonium chlorides in sediment samples

    Science.gov (United States)

    Ferrer, I.; Furlong, E.T.

    2002-01-01

    Benzalkonium chlorides (BACs) were successfully extracted from sediment samples using a new methodology based on accelerated solvent extraction (ASE) followed by an on-line cleanup step. The BACs were detected by liquid chromatography/ion trap mass spectrometry (LC/MS) or tandem mass spectrometry (MS/MS) using an electrospray interface operated in the positive ion mode. This methodology combines the high efficiency of extraction provided by a pressurized fluid and the high sensitivity offered by the ion trap MS/MS. The effects of solvent type and ASE operational variables, such as temperature and pressure, were evaluated. After optimization, a mixture of acetonitrile/water (6:4 or 7:3) was found to be most efficient for extracting BACs from the sediment samples. Extraction recoveries ranged from 95 to 105% for C12 and C14 homologues, respectively. Total method recoveries from fortified sediment samples, using a cleanup step followed by ASE, were 85% for C12BAC and 79% for C14-BAC. The methodology developed in this work provides detection limits in the subnanogram per gram range. Concentrations of BAC homologues ranged from 22 to 206 ??g/kg in sediment samples from different river sites downstream from wastewater treatment plants. The high affinity of BACs for soil suggests that BACs preferentially concentrate in sediment rather than in water.

  9. Optical and electrical characterizations of a single step ion beam milling mesa devices of chloride passivated PbS colloidal quantum dots based film

    Science.gov (United States)

    Hechster, Elad; Shapiro, Arthur; Lifshitz, Efrat; Sarusi, Gabby

    2016-07-01

    Colloidal Quantum Dots (CQDs) are of increasing interest, thanks to their quantum size effect that gives rise to their usage in various applications, such as biological tagging, solar cells and as the sensitizing layer of night vision devices. Here, we analyze the optical absorbance of chloride passivated PbS CQDs as well as revealing a correlation between their photoluminescence and sizes distribution, using theoretical models and experimental results from the literature. Next, we calculate the CQDs resistivity as a film. Although resistivity can be calculated from sheet resistance measurement using four point probes, such measurement is usually carried-out on the layer's surface that in most cases has dangling bonds and surface states, which might affect the charges flow and modify the resistivity. Therefore; our approach, which was applied in this work, is to extract the actual resistivity from measurements that are performed along the film's thickness (z-direction). For this intent, we fabricated gold capped PbS mesas devices using a single step Ion Beam Milling (IBM) process where we milled the gold and the PbS film continually, and then measured the vertical resistance. Knowing the mesas' dimensions, we calculate the resistivity. To the best of our knowledge, no previous work has extracted, vertically, the resistivity of chloride passivated PbS CQDs using the above method.

  10. Design of a Remote Monitoring System for Evaluation of Corrosión in Reinforced Concrete Structures under Chloride Ion Attack

    Directory of Open Access Journals (Sweden)

    Roa-Rodríguez Guillermo

    2015-09-01

    Full Text Available In this paper it was designed and built a remote monitoring equipment that allows to obtain the corrosion potential in reinforcing steels embedded in reinforced concrete, which were previously subjected to chloride attack in a hostile environment. The monitoring system, based on ASTM standard C876-91, determines from 0% to 100% the probability of corrosion on the samples tested. The system provides ease of perform field installation, if there is cellular network coverage, and may be operated remotely using text messages to start and stop measurements, whose results are stored in a local data logger on microSD cards and then are sent via the general packet radio service (GPRS to a web server which allows to access to the data via a web page, where the test results can be seen graphically. The concrete samples used as reference for monitoring degradation were immersed in chloride ion (3.5% NaCl for 12 months. Data for corrosion potential were generated through the exposureconcrete interface, corresponding to a system with a 90% probability of corrosion.

  11. Determination of sodium chloride in ion - exchange membrane caustic soda%离子膜碱中氯化钠的测定

    Institute of Scientific and Technical Information of China (English)

    宋昕; 孙士娟; 邱雪松

    2000-01-01

    The determination of sodium chloride in ion- exchange membrane caustic soda by potentiometry and by spectrophotometry are introduced, and the results obtained by the above two methods are compared. It is concluded that potentiometry is suitable to macro analysis with characteristics of simple operation, rapid analysis and accurate measurement.%介绍了用电位滴定法和分光光度法测定离子膜碱中氯化钠含量的方法,并对这2种方法的测试结果进行了比较。电位滴定法适用于常量分析,具有操作简便、分析速度快、测量结果准确等特点。

  12. Adsorption behavior of poly(dimethyl-diallylammonium chloride) on pulp fiber studied by cryo-time-of-flight secondary ion mass spectrometry and cryo-scanning electron microscopy

    Science.gov (United States)

    Masumi, Takashi; Matsushita, Yasuyuki; Aoki, Dan; Takama, Ruka; Saito, Kaori; Kuroda, Katsushi; Fukushima, Kazuhiko

    2014-01-01

    In this study, the adsorption behavior of poly(dimethyl-diallylammonium chloride) (PDADMAC), a retention agent used in papermaking, in a dual polymer system with anionic poly(acrylamide) (A-PAM) was investigated by time-of-flight secondary ion mass spectrometry (TOF-SIMS). Initially, fragment structures and cleavage patterns were identified via TOF-SIMS experiments with deuterium-labeled PDADMAC and the unlabeled analogue. Visualization of PDADMAC on a dry handsheet surface using traditional TOF-SIMS analysis indicated that the electrostatic interaction between coagulated PDADMAC and A-PAM was relatively weak. A novel cryo-TOF-SIMS/SEM system enabled the evaluation of a wet handsheet containing PDADMAC. Analysis of this sample indicated that PDADMAC adsorbs onto the fiber surface and collects preferentially on the tangled fibrils located between fibers.

  13. Adsorption behavior of poly(dimethyl-diallylammonium chloride) on pulp fiber studied by cryo-time-of-flight secondary ion mass spectrometry and cryo-scanning electron microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Masumi, Takashi [Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho Chikusa-ku, Nagoya, Aichi 464-8601 (Japan); Matsushita, Yasuyuki, E-mail: ysmatsu@agr.nagoya-u.ac.jp [Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho Chikusa-ku, Nagoya, Aichi 464-8601 (Japan); Aoki, Dan [Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho Chikusa-ku, Nagoya, Aichi 464-8601 (Japan); Takama, Ruka [Technical Center, Nagoya University, Furo-cho Chikusa-ku Nagoya, Aichi 464-8601 (Japan); Saito, Kaori [Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho Chikusa-ku, Nagoya, Aichi 464-8601 (Japan); Kuroda, Katsushi [Department of Wood Properties, Forestry and Forest Products Research Institute, 1 Matsunosato, Tsukuba, Ibaraki 305-8687 (Japan); Fukushima, Kazuhiko [Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho Chikusa-ku, Nagoya, Aichi 464-8601 (Japan)

    2014-01-15

    In this study, the adsorption behavior of poly(dimethyl-diallylammonium chloride) (PDADMAC), a retention agent used in papermaking, in a dual polymer system with anionic poly(acrylamide) (A-PAM) was investigated by time-of-flight secondary ion mass spectrometry (TOF-SIMS). Initially, fragment structures and cleavage patterns were identified via TOF-SIMS experiments with deuterium-labeled PDADMAC and the unlabeled analogue. Visualization of PDADMAC on a dry handsheet surface using traditional TOF-SIMS analysis indicated that the electrostatic interaction between coagulated PDADMAC and A-PAM was relatively weak. A novel cryo-TOF-SIMS/SEM system enabled the evaluation of a wet handsheet containing PDADMAC. Analysis of this sample indicated that PDADMAC adsorbs onto the fiber surface and collects preferentially on the tangled fibrils located between fibers.

  14. Las determinaciones genéricas en los procesos adaptativos

    Directory of Open Access Journals (Sweden)

    Pérez Bowie, José Antonio

    2011-04-01

    Full Text Available The translation of a literary text to the screen is usually conditioned by many factors derivated from the new context in which the adapted title must work. Among these we can count the conditions imposed on the original text by the cinematographic genre serving as a model in the translation process. This paper examines the problem and analizes three spanish films of the postwar period in which the literary work experiments an important transformation to adapted to exigences of cinematographic model.

    El traslado de un texto literario a la pantalla suele estar condicionado por diversos factores derivados del nuevo contexto en el que el título adaptado debe funcionar. Entre ellos están los condicionamientos que ejerce sobre la obra originaria el género cinematográfico que sirve de modelo para el proceso adaptador. En el presente trabajo se reflexiona sobre esas determinaciones y se analizan tres ejemplos del cine español de postguerra en los cuales la obra literaria sufre una transformación considerable para adecuarse a las exigencias del modelo cinematográfico elegido.

  15. Influence of heat treatment on microstructure and passivity of Cu–30Zn–1Sn alloy in buffer solution containing chloride ions

    Indian Academy of Sciences (India)

    U Tabrizi; R Parvizi; A Davoodi; M H Moayed

    2012-02-01

    Tin as an alloying element is of great interest in brasses for dezincification impediment. In this paper, Cu–30Zn–1Sn alloy was submitted to three different heat treatments, viz. A (heating up to 800 °C for 20 h, held at 200 °C for 20 h in salt bath and air cooled), B (heating up to 800 °C for 20 h and water quenched) and C (heating up to 600 °C for 20 h and water quenched). The influence of heat treatment on microstructure was evaluated by OM and SEM–EDS analysis. The corrosion resistance in buffer solution (pH 9), H3BO3/Na2B4O7.10H2O, with various concentrations of chloride ions was evaluated by potentiodynamic polarization curves and compared with multicomponent Pourbaix diagrams. A correlation between the heat treatment, microstructure and passivity of the heat treated samples was observed. The results indicated that all heat treatment procedures led to formation of , and -Sn-rich phases as microstructure constituents with a small fraction of ' phase in A. Sn-rich phase appears in grain boundaries and its morphology was slightly changed due to heat treatment. Beneficial influence of low concentration chloride ions on passivity was associated with the formation of copper oxides/hydroxide and chloride complexes. Deterioration was observed at concentrations higher than 0.05 M NaCl due to accelerated dissolution of copper by formation of CuCl$^{−}_{2}$. As a result of dezincification process, preferential corrosion attack and copper redeposition on phase (matrix) were observed. However, Sn-rich (1) phase in grain boundaries was not attacked due to SnO2 formation. In buffer solution, the higher passivity current density in A was related to the presence of small amount of ' phase. On the other hand, in 1 M NaCl, lower critical current density for passivation in B and A (about two times lower than C) was attributed to the grain size effect.

  16. The Cystic Fibrosis Transmembrane Conductance Regulator and Chloride-Dependent Ion Fluxes of Ovine Vocal Fold Epithelium

    Science.gov (United States)

    Leydon, Ciara; Fisher, Kimberly V.; Lodewyck-Falciglia, Danielle

    2009-01-01

    Purpose: Ion-driven transepithelial water fluxes participate in maintaining superficial vocal fold hydration, which is necessary for normal voice production. The authors hypothesized that Cl[superscript -] channels are present in vocal fold epithelial cells and that transepithelial Cl[superscript -] fluxes can be manipulated pharmacologically.…

  17. The simultaneous removal of calcium, magnesium and chloride ions from industrial wastewater using magnesium-aluminum oxide.

    Science.gov (United States)

    Hamidi, Roya; Kahforoushan, Davood; Fatehifar, Esmaeil

    2013-01-01

    In this article, a method for simultaneous removal of calcium, magnesium and chloride by using Mg0.80Al0.20O1.10 as a Magnesium-Aluminum oxide (Mg‒Al oxide) was investigated. Mg‒Al oxide obtained by thermal decomposition of the Mg-Al layered double hydroxide (Mg-Al LDH). The synthesized Mg‒Al oxide were characterized with respect to nitrogen physicosorption, X-ray diffraction (XRD) and field emission scan electron microscopy (FESEM) morphology. Due to high anion-exchange capacity of Mg‒Al oxide, it was employed in simultaneously removal of Cl(-), Mg(+2) and Ca(+2) from distiller waste of a sodium carbonate production factory. For this purpose, experiments were designed to evaluate the effects of quantity of Mg‒Al oxide, temperature and time on the removal process. The removal of Cl(-), Mg(+2) and Ca(+2) from wastewater was found 93.9%, 93.74% and 93.25% at 60°C after 0.5 h, respectively. Results showed that the removal of Cl(-), Mg(+2) and Ca(+2) by Mg‒Al oxide increased with increasing temperature, time and Mg‒Al oxide quantity.

  18. SCC of X-52 and X-60 weldements in diluted NaHCO{sub 3} solutions with chloride and sulfate ions

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Rodriguez, J.G.; Zeferino-Rodriguez, T. [UAEM-Centro de Investigacion en Ingenieria y Ciencias Aplicadas, Av. Universidad 1001, Col. Chamilpa 62210, Cuernavaca, Morelos (Mexico); Espinosa-Medina, M.A.; Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Eje Central Lazaro Cardenas 152, Col. San Bartolo Atepehuacan, 07730 Mexico D. F. (Mexico)

    2007-08-15

    Stress corrosion cracking tests were performed in both X-52 and X-60 weldments in sodium bicarbonate (NaHCO{sub 3}) solutions at 50 C using the Slow Strain Rate Testing (SSRT) technique. Solution concentrations varied between 0.1 to 0.0001 M, and to simulate the NS-4 solution, chloride (Cl{sup -}) and/or sulfate (SO{sub 4}{sup 2-}) ions were added to the 0.01 M solution. Tests were complemented with hydrogen permeation measurements and polarization curves. It was found that the corrosion rate, taken as the corrosion current, I{sub corr}, was maximum in 0.01 M NaHCO{sub 3} and with additions of SO{sub 4}{sup 2-} ions. Higher or lower solution concentrations or additions of Cl{sup -} alone decreased the corrosion rate of the weldment. The SSC susceptibility, measured as the percentage reduction in area, was maximum in 0.01M NaHCO{sub 3}. Higher or lower solution concentrations of additions of Cl{sup -} or SO{sub 4}{sup 2-} decreased the SCC susceptibility of the weldment. The amount of hydrogen uptake for the weldment was also highest in 0.01 M NaHCO{sub 3} solution, but it was minimum with the addition of Cl{sup -} or SO{sub 4}{sup 2-} ions. Thus, the most likely mechanism for the cracking susceptibility of X-52 and X-60 weldments in diluted NaHCO{sub 3} solutions seems to be hydrogen-assisted anodic dissolution. (Abstract Copyright [2007], Wiley Periodicals, Inc.)

  19. 氯离子对硫酸根离子在混凝土中扩散的影响%Chloride ion has an effect on the diffusion of the sulfate ion in the concrete

    Institute of Scientific and Technical Information of China (English)

    王展飞; 杨鼎宜; 俞君宝; 李鹏

    2015-01-01

    It studied the different concentration of chloride ion diffusion in the sulfate ion in the concrete,the influence of single sulfate ion concentration in solution,different chloride ion concentration and sulfate ioncompound solution for erosion solution under continuous soaking on concrete test blocks,and by turbidimetric method to a certain age of sulfate ioncontent in concrete were measured,the results show that the existence of chlorine ion does not change the diffusion rule of sulfate in the concrete,the sulfate gradually reduce with the increase of erosion depth of content;Chlorine salt concentration changes of sulfuric acid root,the influence of the diffusion velocity in concrete have larger sulfate diffusion velocity in concrete increased with the increase of chlorine salt concentration decreased.%研究了不同氯离子浓度对硫酸根在混凝土中扩散的影响,以单一硫酸根离子浓度溶液、不同氯离子浓度与硫酸根离子为复合溶液作为侵蚀溶液对混凝土试块进行连续浸泡,采用比浊法对一定龄期的混凝土中的硫酸根离子含量进行测定,结果表明:氯离子的存在并不改变硫酸根在混凝土中的扩散规律,即硫酸根随着侵蚀深度的增加含量逐渐减少;氯盐浓度变化对硫酸根在混凝土中的扩散速度有较大的影响,硫酸根在混凝土中扩散速度随着氯盐浓度的增加而下降。

  20. Durability of API class B cement pastes exposed to aqueous solutions containing chloride, sulphate and magnesium ions

    Directory of Open Access Journals (Sweden)

    Hernández, M. E.

    2008-12-01

    Full Text Available This paper discusses a durability study conducted on API class B cement, the type used in shallow oil wells, when exposed to aggressive formation water. Its resistance to the major ions, namely –SO4=, Mg+2 and Cl-–, is related both to its capacity to assimilate the aggressive action of each harmful agent and to the changes in the chemical reactivity of some of its components. The methodology used consisted in preparing and immersing cement specimens in neutral solutions containing variable concentrations of these ions to monitor the chemical reactions taking place. These solutions were analyzed and XRD studies were conducted for over a year to identify mineralogical variations. The purposes of the study were to determine the effects of joint ionic attack on this kind of cement and to monitor the variations in the calcium concentration in the aqueous solutions of Na2SO4, MgCl2 and NaCl in contact with API class B cement pastesEste trabajo se basa en el estudio de la durabilidad de un cemento API clase B, utilizado en pozos petrolíferos someros, frente a la agresividad de las aguas de formación a las que puede estar expuesto. Su eficacia frente a la exposición a los iones más importantes –SO4=, Mg+2 y Cl-– se relaciona con su capacidad de asimilar la acción agresiva de cada agente perjudicial, así como de las reacciones químicas que sufra por la reactividad de alguno de sus compuestos. La metodología aplicada supone la preparación de probetas de este cemento y su inmersión en disoluciones neutras, conteniendo los referidos iones a distintas concentraciones, para evaluar el desarrollo de las reacciones existentes en su seno. A tal fin se realizaron análisis de las disoluciones y estudios de DRX durante más de un año para conocer su evolución mineralógica. El objetivo del trabajo ha sido determinar los efectos resultantes de los ataques conjuntos de los citados iones al referido cemento; así como la observación de las

  1. 烧伤回吸期持续性高钠高氯与侵袭性感染%Persistent High Level of Sodium and Chloride Ions and Invasive Infection in Resorption Phase Postburn

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    目的:探讨大面积烧伤患者持续性高钠高氯产生的原因及防治措施;动态监测大面积烧伤后血清Na+,Cl-的临床意义。方法:回顾性分析了7例严重烧伤后持续性高Na+高Cl-和61例严重烧伤后非持续性高Na+,高Cl-患者的临床特点。结果:7例严重烧伤后持续高Na+,高Cl-患者均有严重侵袭性感染;且高Na+出现愈早,上升愈快,则感染愈重,愈后愈差。结论:1.烧伤后持续性高Na+,高Cl-产生的原因是严重侵袭性感染。2.动态监测血清Na+Cl-对感染的评价及抗感染效果有积极意义。3.预防措施包括平稳渡过休克,保护创面,避免长途转运。治疗上一旦出现持续性高钠高氯,除对症治疗外,根本措施是创面处理及抗感染。%Objective: To investigate the cause persistent high level of sodium and chloride ions in serum and methods for its prevention and treatment. The clinical significance of dynamic monitoring of serum sodium and chloride ion levels in severe burn patients. Method: To make a review of 7 cases with persistent high serum sodium and chloride ion levels and 61 cases without. Results: All of the severe cases had invasive infection. The earlier the presence of high serum sodium and chloride ion levels, the more dangerous the case. Conclusion: 1. Persistent high serum sodium and chloride ion levels is caused by invasive infection. 2. Dynamic monitoring of serum sodium and chloride ion levels is of great clinical significance. 3. Prevention measures include: to tide over shock stage, to protect burn wounds, to avoid long distance transfer. 4. Treating measures include careful management of burn wounds, anti-infection and expectant treatment.

  2. 海洋水下区喷射混凝土中氯离子扩散性能研究%Experimental research on chloride ion erosion of shotcret in the marine underwater area

    Institute of Scientific and Technical Information of China (English)

    周宇; 牛荻涛; 王家滨

    2014-01-01

    Sprayed concrete structure is an important part of tunnel support.Located in the marine environment tunnel project is bound to suffer the erosion of chloride ions.Amethod to simulate the indoor soaking underwater marine environment to spray concrete chloride ion diffusion performance difference with ordinary concrete core,concrete way affect the main chloride diffusion of concrete performance.The test results show that construction methods on the performance of concrete resistance to chloride ion penetration significantly.Compared to ordinary concrete,shotcrete depth slightly largercapillary adsorption zone,the chloride ion concentration peak of about 2.51 times that of ordinary concrete,the larger chloride ion diffusion rate.After the addition of steel fibers ,sprayed concrete resistance to chloride ion pene-tration increased.Fick's second law onthe use of sprayed concrete in chloride ion content in non-linear fitting,with good correlation,and the initial establishment of the sprayed concrete and ordinary concrete chloride ion diffusion coefficient of relationship.%喷射混凝土结构是隧道支护的重要组成部分。位于海洋环境中的隧道工程,势必遭受氯离子的侵蚀。采用室内浸泡的方法模拟海洋水下环境,以喷射混凝土与普通混凝土中氯离子扩散性能差异为核心,主要研究混凝土施工方式对混凝土中氯离子扩散性能的影响。试验结果表明:施工方式对混凝土的抗氯离子渗透性能影响显著。相对于普通混凝土,喷射混凝土毛细吸附区深度略大,氯离子浓度峰值约为普通混凝土的2.51倍,氯离子扩散速率较大。加入钢纤维后,喷射混凝土抗氯离子渗透性能有所提高。运用Fick第二定律对喷射混凝土中氯离子含量进行非线性拟合,具有良好相关性,并初步建立了喷射混凝土与普通混凝土氯离子扩散系数的关系。

  3. Chronopotentiometric chloride sensing using transition time measurement

    NARCIS (Netherlands)

    Abbas, Y.; Graaf, de D.B.; Olthuis, W.; Berg, van den A.

    2013-01-01

    Detection of chloride ions is crucial to accurately access the concrete structure durability[1]. The existing electrochemical method of chloride ions detection in concrete, potentiometry[1], is not suitable for in-situ measurement due to the long term stability issue of conventional reference electr

  4. DNA-gelatin complex coacervation, UCST and first-order phase transition of coacervate to anisotropic ion gel in 1-methyl-3-octylimidazolium chloride ionic liquid solutions.

    Science.gov (United States)

    Rawat, Kamla; Aswal, V K; Bohidar, H B

    2012-12-27

    Study of kinetics of complex coacervation occurring in aqueous 1-octyl-3-methylimidazolium chloride ionic liquid solution of low charge density polypeptide (gelatin A) and 200 base pair DNA, and thermally activated coacervate into anisotropic gel transition, is reported here. Associative interaction between DNA and gelatin A (GA) having charge ratio (DNA:GA = 16:1) and persistence length ratio (5:1) was studied at fixed DNA (0.005% (w/v)) and varying GA concentration (C(GA) = 0-0.25% (w/v)). The interaction profile was found to be strongly hierarchical and revealed three distinct binding regions: (i) Region I showed DNA-condensation (primary binding) for C(GA) coacervation. (iii) Region III (0.15 coacervate was found to be protein concentration specific in Raman studies. The binding profile of DNA-GA complex with IL concentration revealed optimum IL concentration (=0.05% (w/v)) was required to maximize the interactions. Small angle neutron scattering (SANS) data of coacervates gave static structure factor profiles, I(q) versus wave vector q, that were remarkably similar and invariant of protein concentration. This data could be split into two distinct regions: (i) for 0.0173 coacervate phase resided close to the gelation state of the protein. Thus, on a heating-cooling cycle (heating to 50 °C followed by cooling to 20 °C), the heterogeneous coacervate exhibited an irreversible first-order phase transition to an anisotropic ion gel. This established a coacervate-ion gel phase diagram having a well-defined UCST.

  5. Ionisation and dissociation of diarylmethyl chlorides in BCl/sub 3/CH/sub 2/Cl/sub 2/ solution: Spectroscopic evidence for carbenium ion pairs

    Energy Technology Data Exchange (ETDEWEB)

    Schneider, R.; Mayr, H.; Plesch, P.H.

    1987-12-01

    The ionisation equilibria of diarylmethyl chlorides Ar/sub 2/CHCl (Ar = p-CH/sub 3/O-C/sub 6/H/sub 4/, p-PhO-C/sub 6/H/sub 4/, p-CH/sub 3/-C/sub 6/H/sub 4/) reacting with BCl/sub 3/ in CH/sub 2/Cl/sub 2/ to give ion-pairs Ar/sub 2/CH/sup +/BCl/sub 4//sup -/ (K/sub 1/), and the dissociation of these (K/sub D/) were studied by conductimetry and spectro-photometry. The molar conductivities are almost independent of the nature of the aryl group (approx. = 3.5.10/sup -3/ Sm/sup 2/mol at -70/sup 0/C). The ionisation constants K/sub I/ increase strongly with increasing electron releasing ability of the p-substituents. The standard ionisation enthalpies and entropies for (p-CH/sub 3/-C/sub 6/H/sub 4/)/sub 2/CHCl and (p-PhO-C/sub 6/H/sub 4/)(Ph)CHCl, calculated from the K/sub I/ at different temperatures are negative. The dissociation constants K/sub D/ ((1.9-2.9).10/sup -4/ molL at -70/sup 0/C) do not show a systematic dependence on the electron donating abilities of the substituents in the aryl groups. Small differences between the UV-vis absorption spectra of unpaired and paired ions were used to confirm the conductimetrically determined values of K/sub D/.

  6. EXPERIMENTAL STUDY ON THE PENETRATION OF CHLORIDE IONS INTO HIGH PERFORMANCE CONCRETE%高性能混凝土氯离子渗透性能的试验研究

    Institute of Scientific and Technical Information of China (English)

    盛黎; 姚谏

    2011-01-01

    Using the ASTM C1202 method and the NEL method,the experimental study on the impermeability to chloride ions of high performance concrete was performed,including high performance concrete mixed with only slag and mixed with compound mineral admixture.The correlations between electric flux and chloride diffusion coefficient were discussed.Test result indicated that the mineral admixture can effectively raise the ability to resist chloride ion penetration into high performance concrete.Mixing slag and fly ash especially could more effectively improve the impermebibty to chloride ions of the high performance concrete,and good correlation between electric flux and chloride diffusion coefficient was also showed.When water cement ratio was smaller,the correlation between the two indexes was better.%采用ASTM C1202法及NEL法,对单掺矿渣和复掺粉煤灰、矿渣的高性能混凝土进行抗氯离子渗透性能的试验研究,并探讨电通量与氯离子扩散系数之间的相关性。结果表明:矿物掺合料能有效地改善高性能混凝土的抗氯离子渗透性能,复掺粉煤灰和矿渣比单掺矿渣的效果更佳;电通量与氯离子扩散系数之间具有较好的相关性,当水胶比较小时,两指标间的相关性更好。

  7. Surface-enhanced Raman scattering and atomic force microscopy of brass electrodes in sulfuric acid solution containing benzotriazole and chloride ion

    Energy Technology Data Exchange (ETDEWEB)

    Rubim, J.C.; Kim, J.; Henderson, E.; Cotton, T.M. (Instituto de Quimica da Universidade de Sao Paulo (Brazil) Ames Lab., IA (United States) Iowa State Univ., Ames (United States))

    1993-01-01

    Three different methods were used to roughen brass (Cu/Zn = 67/33) electrodes in 0.5 M H[sub 2]SO[sub 4] containing 1.0 mM benzotriazole (BTAH): (1) polarization at +0.05 V vs. saturated calomel for 5 min; (2) immersion in the above solution for six hours; and (3) oxidation-reduction cycling in the presence of chloride ion. The surfaces prepared by the first two methods exhibited surface-enhanced Raman scattering (SERS) spectra of the polymeric complex [Cu(I)BTA][sub s]. The SERS spectrum obtained from electrodes prepared by the third method is very similar to that of [Cu(I)CIBTAH][sub 4]. Examination of the electrodes by atomic force microscopy (AFM) showed that a large number of grain boundary sites are formed by the roughening processes. This effect is attributed to the loss of zinc, which occurs during corrosion of the mirror-like, polished brass electrode surface in the sulfuric acid solution. 11 refs., 5 figs.

  8. Carboxylated graphene oxide/polyvinyl chloride as solid-phase extraction sorbent combined with ion chromatography for the determination of sulfonamides in cosmetics.

    Science.gov (United States)

    Zhong, Zhixiong; Li, Gongke; Luo, Zhibin; Liu, Zhe; Shao, Yijuan; He, Wanwen; Deng, Jianchao; Luo, Xingling

    2015-08-12

    A carboxylated graphene oxide/polyvinyl chloride (CGO/PVC) material was prepared as a sorbent for the selective extraction of sulphonamides from complex sample. After being dispersed in buffer solution, sample was transferred into the prefabricated solid-phase extraction (SPE) column, which integrated extraction and cleanup into one single-step. A multi-response optimization based on the Box-Behnken design was used to optimize factors affecting extraction efficiency. Compared with the commonly commercial sorbents including MCX, WCX and C18, CGO/PVC hybrid material had higher extraction selectivity and capacity to sulphonamides. The limits of detection and quantification for seven target compounds were in the range of 3.4-7.1 μg/L and 11.4-23.7 μg/L, respectively. The self-assembly SPE cartridge was successfully used to enrich seven analytes in anti-acne cosmetics prior to ion chromatography detection with good recoveries of 87.8-102.0% and relative standard deviations of 1.2-6.4%, implying that this method was suitable for routine analysis of cosmetics.

  9. Simultaneous analysis of apolar phytohormones and 1-aminocyclopropan-1-carboxylic acid by high performance liquid chromatography/electrospray negative ion tandem mass spectrometry via 9-fluorenylmethoxycarbonyl chloride derivatization.

    Science.gov (United States)

    Ziegler, Jörg; Qwegwer, Jakob; Schubert, Melvin; Erickson, Jessica L; Schattat, Martin; Bürstenbinder, Katharina; Grubb, C Douglas; Abel, Steffen

    2014-10-03

    A strategy to detect and quantify the polar ethylene precursor 1-aminocyclopropan-1-carboxylic acid (ACC) along with the more apolar phytohormones abscisic acid (ABA), indole-3-acetic acid (IAA), jasmonic acid (JA), jasmonic acid-isoleucine conjugate (JA-Ile), 12-oxo-phytodienoic acid (OPDA), trans-zeatin, and trans-zeatin 9-riboside using a single extraction is presented. Solid phase resins commonly employed for extraction of phytohormones do not allow the recovery of ACC. We circumvent this problem by attaching an apolar group to ACC via derivatization with the amino group specific reagent 9-fluorenylmethoxycarbonyl chloride (Fmoc-Cl). Derivatization in the methanolic crude extract does not modify other phytohormones. The derivatized ACC could be purified and detected together with the more apolar phytohormones using common solid phase extraction resins and reverse phase HPLC/electrospray negative ion tandem mass spectrometry. The limit of detection was in the low nanomolar range for all phytohormones, a sensitivity sufficient to accurately determine the phytohormone levels from less than 50mg (fresh weight) of Arabidopsis thaliana and Nicotiana benthamiana tissues. Comparison with previously published phytohormone levels and the reported changes in phytohormone levels after stress treatments confirmed the accuracy of the method.

  10. Analysis of amino acids by HPLC/electrospray negative ion tandem mass spectrometry using 9-fluorenylmethoxycarbonyl chloride (Fmoc-Cl) derivatization.

    Science.gov (United States)

    Ziegler, Jörg; Abel, Steffen

    2014-12-01

    A new method for the determination of amino acids is presented. It combines established methods for the derivatization of primary and secondary amino groups with 9-fluorenylmethoxycarbonyl chloride (Fmoc-Cl) with the subsequent amino acid specific detection of the derivatives by LC-ESI-MS/MS using multiple reaction monitoring (MRM). The derivatization proceeds within 5 min, and the resulting amino acid derivatives can be rapidly purified from matrix by solid-phase extraction (SPE) on HR-X resin and separated by reversed-phase HPLC. The Fmoc derivatives yield several amino acid specific fragment ions which opened the possibility to select amino acid specific MRM transitions. The method was applied to all 20 proteinogenic amino acids, and the quantification was performed using L-norvaline as standard. A limit of detection as low as 1 fmol/µl with a linear range of up to 125 pmol/µl could be obtained. Intraday and interday precisions were lower than 10 % relative standard deviations for most of the amino acids. Quantification using L-norvaline as internal standard gave very similar results compared to the quantification using deuterated amino acid as internal standards. Using this protocol, it was possible to record the amino acid profiles of only a single root from Arabidopsis thaliana seedlings and to compare it with the amino acid profiles of 20 dissected root meristems (200 μm).

  11. Functional modulation of cerebral gamma-aminobutyric acidA receptor/benzodiazepine receptor/chloride ion channel complex with ethyl beta-carboline-3-carboxylate: Presence of independent binding site for ethyl beta-carboline-3-carboxylate

    Energy Technology Data Exchange (ETDEWEB)

    Taguchi, J.; Kuriyama, K. (Kyoto Prefectural Univ. of Medicine (Japan))

    1990-05-01

    Effect of ethyl beta-carboline-3-carboxylate (beta-CCE) on the function of gamma-aminobutyric acid (GABA)A receptor/benzodiazepine receptor/chloride ion channel complex was studied. Beta-CCE noncompetitively and competitively inhibited (3H)flunitrazepam binding to benzodiazepine receptor, but not (3H)muscimol binding to GABAA receptor as well as t-(3H)butylbicycloorthobenzoate (( 3H) TBOB) binding to chloride ion channel, in particulate fraction of the mouse brain. Ro15-1788 also inhibited competitively (3H) flunitrazepam binding. On the other hand, the binding of beta-(3H)CCE was inhibited noncompetitively and competitively by clonazepam and competitively by Ro15-1788. In agreement with these results, benzodiazepines-stimulated (3H)muscimol binding was antagonized by beta-CCE and Ro15-1788. Gel column chromatography for the solubilized fraction from cerebral particulate fraction by 0.2% sodium deoxycholate (DOC-Na) in the presence of 1 M KCl indicated that beta-(3H)CCE binding site was eluted in the same fraction (molecular weight, 250,000) as the binding sites for (3H)flunitrazepam, (3H)muscimol and (3H)TBOB. GABA-stimulated 36Cl- influx into membrane vesicles prepared from the bovine cerebral cortex was stimulated and attenuated by flunitrazepam and beta-CCE, respectively. These effects of flunitrazepam and beta-CCE on the GABA-stimulated 36Cl- influx were antagonized by Ro15-1788. The present results suggest that the binding site for beta-CCE, which resides on GABAA receptor/benzodiazepine receptor/chloride ion channel complex, may be different from that for benzodiazepine. Possible roles of beta-CCE binding site in the allosteric inhibitions on benzodiazepine binding site as well as on the functional coupling between chloride ion channel and GABAA receptor are also suggested.

  12. Source apportionment of chloride ions in the indoor air in Tian Bay nuclear power plant%田湾核电站室内氯离子来源解析

    Institute of Scientific and Technical Information of China (English)

    陈发荣; 田黎; 郑立; 赵恒强; 何鹰; 郑晓玲; 王小如

    2014-01-01

    Concentration of chloride ions in the atmospheric absorbed solution (AAS) and total suspended particles (TSP) samples collected in Tian Bay nuclear power plant between 2005 and 2006 was determined by the way of ion chromatography. The distributions and variations of chloride ions in the indoor and outdoor air and the performance of air filter were also investigated. The results showed that the annual average concentrations of chloride ions were 28.12, 19.20, 4.22 and 0.11µg/m3in the outdoor AAS, indoor AAS, outdoor TSP and indoor TSP, respectively. The outdoor TSP could be effectively filtered by the existing air filter, but the filter efficiency of chloride ions in the outdoor air was only 32%. Besides, there was a significant positive correlation between the outdoor AAS and indoor AAS, and the correlation coefficien was 0.859. Therefore, it could be inferred that the chloride ions in the indoor air mainly came from outdoor sources.%根据2005~2006年江苏田湾核电站大气吸收液(AAS)和总悬浮颗粒物(TSP)中氯离子的一年数据,分析了室内外大气各种形态氯离子的分布特点及变化规律,并对过滤器性能进行了初步评价.结果表明:该站大气氯离子浓度大小依次为:室外吸收液>室内吸收液>室外TSP>室内TSP,年均值分别为28.12,19.20,4.22,0.11µg/m3.现有过滤器可以有效过滤室外总悬浮颗粒物,但对室外气体中氯离子的过滤效率仅为32%.相关性分析表明,室内外吸收液中氯离子浓度显著相关,相关性系数为0.859.因此,室内大气氯离子主要来源室外气态或微小气溶胶.

  13. Applied Research on Field Test Method for Concrete Resistance to Chloride Ion Penetration%现场测试混凝土抗氯离子渗透性方法的应用研究

    Institute of Scientific and Technical Information of China (English)

    王娜; 李俊毅; 张鹏; 杨建军; 雷周

    2011-01-01

    为快速、准确地测定混凝土中氯离子的含量,以实现对混凝土耐久性的有效评价和钢筋腐蚀的适时防护与有效修复,研究现场测试氯离子渗透性的方法是非常必要的.结合客运专线工程施工情况,分别按矿物掺合料不同掺量以及不同的强度等级进行配合比设计试验,采用PERMIT离子迁移仪对混凝土试件进行氯离子扩散系数的测定,并采用电通量法进行验证.结果表明:随着电通量的增加,氯离子扩散系数呈现增加的趋势,二者存在很好的线性关系;双掺粉煤灰+矿粉的混凝土抗氯离子侵入性优于单掺粉煤灰的混凝土;PERMIT离子渗透试验方法测得的试验结果准确可靠,具有很强的实用性.可以为混凝土耐久性的判定提供依据.%For rapid and accurate determination of chloride content in concrete to achieve the effective evaluation of the durability of concrete and steel corrosion protection and effective timely repair. The study of chloride ion permeability field test method is very necessary. Combining with the construction works of a passenger railway line, mix ratio tests were designed respectively for concrete with different contents of mineral admixtures and different strength grades. PERMIT ion mobility instrument was used to determine the chloride ion diffusion coefficient of concrete specimens. The results show that, with the increase of electric flux, chloride ion diffusion coefficient showed an increasing trend, both with good linear relationship. Fly ash and slag concrete resistance to ingress of chloride ions was better than concrete singly added with fly ash. The measured test results of PERMIT ion penetration test method are accurate and reliable, and highly practical. It can provide basis for determining the durability of concrete.

  14. Differential sensitivity to chloride and sodium ions in seedlings of Glycine max and G. soja under NaCl stress.

    Science.gov (United States)

    Luo, Qingyun; Yu, Bingjun; Liu, Youliang

    2005-09-01

    High Na+ and Cl- concentrations in soil cause hyperionic and hyperosmotic stress effects, the consequence of which can be plant demise. Ion-specific stress effects of Na+ and Cl- on seedlings of cultivated (Glycine max (L.) Merr) and wild soybean (Glycine soja Sieb. Et Zucc.) were evaluated and compared in isoosmotic solutions of Cl-, Na+ and NaCl. Results showed that under NaCl stress, Cl- was more toxic than Na+ to seedlings of G. max. Injury of six G. max cultivars, including 'Jackson' (salt sensitive) and 'Lee 68' (salt tolerant), was positively correlated with the content of Cl- in the leaves, and negatively with that in the roots. In subsequent research, seedlings of two G. max cultivars (salt-tolerant Nannong 1138-2, and salt-sensitive Zhongzihuangdou-yi) and two G. soja populations (BB52 and N23232) were subjected to isoosmotic solutions of 150mM Na+, Cl- and NaCl, respectively. G. max cv. Nannong 1138-2 and Zhongzihuangdou-yi were damaged much more heavily in the solution of Cl- than in that of Na+. Their Leaves were found to be more sensitive to Cl- than to Na+, and salt tolerance of these two G. max cultivars was mainly due to successful withholding of Cl- in the roots and stems to decrease its content in the leaves. The reverse response to isoosmotic stress of 150 mM Na+ and Cl- was shown in G. soja populations of BB52 and N23232; their leaves were not as susceptible to toxicity of Cl- as that of Na+. Salt tolerance of BB52 and N23232 was mainly due to successful withholding of Na+ in the roots and stems to decrease its content in the leaves. These results indicate that G. soja have advantages over G. max in those traits associated with the mechanism of Cl-tolerance, such as its withholding in roots and vacuoles of leaves. It is possible to use G. soja to improve the salt tolerance of G. max.

  15. Effects of sodium chloride exposure on ion regulation in larvae (glochidia) of the freshwater mussel Lampsilis fasciola.

    Science.gov (United States)

    Nogueira, Lygia S; Bianchini, Adalto; Wood, Chris M; Loro, Vania L; Higgins, Sarah; Gillis, Patricia L

    2015-12-01

    The salinization of freshwater can have negative effects on ecosystem health, with heightened effects in salt-sensitive biota such as glochidia, the larvae of freshwater mussels. However, the toxicological mechanism underlying this sensitivity is unknown. Therefore, Lampsilis fasciola glochidia were exposed to NaCl (nominally 0.25 and 1.0 g/L) prepared in reconstituted moderately-hard water (control), as well as to a dilution of that water (1:4) with ultrapure reference water (diluted control). Unidirectional Na(+) influx (measured with (22)Na) was evaluated after 1, 3 and 48 h of exposure. In addition, unidirectional Cl(-) influx (measured with (36)Cl), whole-body ion (Cl(-) and Na(+)) concentrations, and glochidia viability (measured as the ability to close valves) were assessed after 48 h of exposure. Significantly reduced glochidia viability (56%) was observed after exposure to 1.0 g/L NaCl. Na(+) influx was significantly higher in glochidia exposed to both 0.25 and 1.0 g/L NaCl for 1h than in those kept under control conditions. After 3 and 48 h of exposure, differences in Na(+) influx rate between salt-exposed and control glochidia were generally reduced, indicating that larvae may be able to, at least temporarily, recover their ability to regulate Na(+) influx when exposed to elevated NaCl concentration. Compared to the moderately-hard water control, whole-body Na(+) and Cl(-) concentrations were relatively unchanged in glochidia exposed to 0.25 g/L NaCl, but were significantly elevated in glochidia exposed to 1.0 g/L NaCl and the diluted control. While Na(+) influx rate had recovered to the control level after 48 h of exposure to 1.0 g/L NaCl, Cl(-) influx rate remained elevated, being ~7-fold higher than the Na(+) influx rate. These findings suggest that the loss of viability observed when glochidia were exposed to a high NaCl concentration (1.0 g/L) could be caused by ionoregulatory disturbances mainly associated with an elevated Cl(-) influx.

  16. Determination of the hydrolysis constants of Europium (III), in ion strength media 4, 5 and 6 M NaClO{sub 4} at 303 K; Determinacion de las constantes de hidrolisis del Europio (III), en medios de fuerza ionica 4, 5 y 6 M de NaClO{sub 4} a 303 K

    Energy Technology Data Exchange (ETDEWEB)

    Alvarado B, A.; Jimenez R, M.; Solache R, M. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

    1999-07-01

    This work was made with the purpose to complete information about the hydrolysis constants of Europium (III) in high ion strength media. So it was determined at a ion forces media 4, 5 and 6 M of sodium perchlorate at 303 K. The method used was the potentiometric with the aid of the Super quad computer program. In high ion strength media, the measurements of p H do not correspond directly to negative logarithm of the concentration of hydrogen ions, by this it is necessary to calibrate the electrode in these conditions. The Europium was hydrolized at pC{sub H} values greater 6 in all cases. The potentiometric method used under the described experimental conditions is adequate to determine the hydrolysis constants of Europium (III). According to the results and diagrams of chemical species of Europium obtained we can conclude that the hydrolysis constants, differ by its distribution but not in its identity. (Author)

  17. Sensitivity Analysis of Chloride Ion Diffusion in Concrete Subjected to Marine Environment%海工环境混凝土中氯离子扩散敏感性分析

    Institute of Scientific and Technical Information of China (English)

    郝风田; 路影

    2013-01-01

    The sufficient attention may be paid attention to the durability of reinforced concrete structure all over the world at present .The concrete structures would be subjected to chloride ingress ,resulting in the corrosion of reinforcing bars ,inducing early deterioration and losing their durability ,and this is a main problem in engineering practices .Based on the second Fick’s law ,and taking into account the surface chloride concentration ,temperature ,water cement ratio , and initial chloride content ,the chloride ion diffusion is calculated and analyzed here .The sensitivity analysis shows that the influence factors of surface chloride concentration ,temperature ,water cement ratio of concrete are obvious ,and the influence of initial chloride content is weaker .%混凝土结构耐久性问题是当今世界普遍关注的问题。由于氯离子侵蚀,导致钢筋锈蚀,使结构发生早期破坏,丧失了结构的耐久性能,已成为实际工程中的重要问题。基于 Fick 第二定律,分别考虑表面氯离子浓度、温度、水灰比、初始氯离子含量,计算氯离子扩散。敏感性分析表明表面氯离子浓度、温度、水灰比对混凝土中氯离子扩散影响较大,初始氯离子含量影响较小。

  18. 影响混凝土氯离子电通量因素的试验研究与分析%Experimental Study and Analysis of Influencing Factors on Concrete's Chloride Ion Penetration

    Institute of Scientific and Technical Information of China (English)

    张勇; 杜修力; 李悦

    2013-01-01

    选用国内具有代表性的铁道工程混凝土配合比,按照铁道行业混凝土电通量测试方法,对影响混凝土氯离子电通量变化的各因素进行了一系列试验.结果表明,试件养护龄期、掺合料掺量和掺合料品种是影响混凝土电通量的主要因素.混凝土的电通量随养护龄期的持续延长而逐渐降低,采用56 d养护龄期评定测试结果比较合理.电通量随着粉煤灰和矿粉掺量的增加呈现降低的趋势,粉煤灰降低电通量效果优于矿粉,掺量达到40%时两者效果接近.混凝土配合比其他参数如水胶比、含气量、水泥和减水剂品种对电通量的影响较小.%Based on representative concrete design mixes used in the domestic railway project, the concrete's chloride-ion penetration is studied and its influencing factors are also analyzed. Results show that concrete curing age, type, and volume of mineral admixtures are the main influencing factors of concrete's chloride ion penetration. With the concrete curing age extending, the chloride-ion penetration value lowers and it is reasonable to evaluate test results through curing age of 56 days. Adding the volume of fly ash and ground granulated blast furnace slag( GGBS) , the chloride-ion penetration value declines. The effect of reducing concrete's chloride ion penetration of fly ash is much better than that of GGBS, and both effects are almost equal when the volume reaches 40% . Other concrete mixed parameters, such as water binder ratio, air content, and types of cement and super plasticizers are less important influencing factors.

  19. Preparation of Copper Telluride Films by Co-Reduction of Cu(I) and Te(IV) Ions in Choline Chloride: Ethylene Glycol Ionic Liquid

    Science.gov (United States)

    Golgovici, Florentina; Catrangiu, Adriana-Simona; Stoian, Andrei Bogdan; Anicai, Liana; Visan, Teodor

    2016-07-01

    Cathodic processes of direct co-reduction of Cu+ and Te4+ ions on Pt electrode at 60°C were investigated using cyclic voltammetry and electrochemical impedance spectroscopy techniques. The ionic liquid as background electrolyte consisted of a mixture of choline chloride and ethylene glycol (ChCl-EG 1:2 mol ratio) in which 5-20 mM CuCl and 8 mM TeO2 were dissolved. The voltammograms exhibited the following successive cathodic processes: Cu2+/Cu+ reduction, Te underpotential deposition, simultaneous deposition of Cu metal and CuTe compound, and deposition of Te-rich CuTe compound at the most negative potentials (from -0.5 V to -0.8 V). Corresponding dissolution or oxidation peaks were recorded on the anodic branch. The voltammetric results were confirmed by electrochemical impedance spectra. Copper telluride films have been synthesized on platinum substrate via potentiostatic electrodeposition at 60°C. It was found from atomic force microscopy that CuTe film samples prepared from ChCl-EG + 5 mM CuCl + 8 mM TeO2 ionic liquid have high growth rates. The x-ray diffraction patterns of the deposited films from ChCl-EG + 10 mM CuCl + 8 mM TeO2 ionic liquid indicated the presence of a Cu2Te phase for film deposited at -0.7 V and a Cu0.656Te0.344 phase for film deposited at -0.6 V.

  20. Diagnosis of drowning by summation of sodium, potassium and chloride ion levels in pleural effusion: differentiating between freshwater and seawater drowning and application to bathtub deaths.

    Science.gov (United States)

    Yajima, Daisuke; Saito, Hisako; Sato, Kaoru; Hayakawa, Mutsumi; Iwase, Hirotaro

    2013-12-10

    Although electrolyte analysis of pleural effusion at autopsy is useful for the diagnosis of water aspiration (i.e., drowning), the method of comparing each level of sodium (Na(+)), potassium (K(+)), and chloride (Cl(-)) ions does not clearly differentiate between freshwater drowning, seawater drowning, and non-drowning. Therefore, here we introduce the summation of Na(+), K(+), and Cl(-) levels, that is SUM(Na+K+Cl), as a modified diagnostic indicator. In 21 autopsy cases of freshwater drowning, 32 cases of seawater drowning, and 43 non-drowning controls (with pleural effusion), mean SUM(Na+K+Cl) differed significantly between the groups (188.8±33.2, 403.5±107.9, and 239.3±21.7 mEq/L, respectively). We defined a SUM(Na+K+Cl) cut-off value of 282.7 mEq/L as strongly suggestive of seawater aspiration. When these values were applied to the two drowning groups, 15 cases (71%) of freshwater drowning and 29 cases (91%) of seawater drowning were diagnosed correctly. This new approach may be more valid than previous methods in cases found >2 days after death or those with substantial pleural effusion (>100 mL). For an additional 15 bathtub deaths, mean SUM(Na+K+Cl) was 198.8±40.0 mEq/L, and in 14 of these cases (93%) the relationship between cause of death and SUM(Na+K+Cl) could be explained using this method. Forensic pathologists should not depend exclusively on chemical findings and should consider also typical pathological indicators of drowning. This new method may be useful as a supplementary diagnostic tool when used alongside consideration of the pathological findings.

  1. A comprehensive probabilistic model of chloride ingress in unsaturated concrete

    OpenAIRE

    Bastidas-Arteaga, Emilio; Chateauneuf, Alaa; Sánchez-Silva, Mauricio; Bressolette, Philippe; Schoefs, Franck

    2011-01-01

    International audience; Corrosion induced by chloride ions has become a critical issue for many reinforced concrete structures. The chloride ingress into concrete has been usually simplified as a diffusion problem where the chloride concentration throughout concrete is estimated analytically. However, this simplified approach has several limitations. For instance, it does not consider chloride ingress by convection which is essential to model chloride penetration in unsaturated conditions as ...

  2. Determination of Choline Chloride by Ion Chromatography and Infrared Spectroscopy%离子色谱法结合红外光谱法检验氯化琥珀胆碱

    Institute of Scientific and Technical Information of China (English)

    乔文涛; 黄彬晏; 黄克建; 刘晓锋; 杨宁; 易叶平

    2014-01-01

    建立了离子色谱法结合红外光谱法检验案件中氯化琥珀胆碱的分析方法。用离子色谱法使离子分离后,采用电导检测器检测,同时结合红外光谱法将检材样品挥干后与溴化钾压片用红外光谱仪检测。结果表明,该方法能从案件检材中检出氯化琥珀胆碱成分,相似度达到96%。所建立的方法操作简单,检测灵敏,结果准确,可用于刑事案件中检材的快速检验。%A method for detecting choline chloride in biological samples by ion chromatography and infrared spectroscopy was established. Ion exchange chromatography was used to separate ions from analysis column, and the ions were detected by using conductivity detector. In the same time, the samples were detected by infrared spectroscopy. The results showed that this method could detect choline chloride from case samples, and the similarity of retrieval reached 96%. The method is simple, sensitive and accurate, it can be used for rapid detection in casework.

  3. Discrete-state representation of ion permeation coupled to fast gating in a model of CLC-chloride channels: analytic estimation of the state-to-state rate constants.

    Science.gov (United States)

    Coalson, Rob D; Cheng, Mary Hongying

    2011-09-01

    Analytical estimation of state-to-state rate constants is carried out for a recently developed discrete state model of chloride ion motion in a CLC chloride channel (Coalson and Cheng, J. Phys. Chem. B 2010, 114, 1424). In the original presentation of this model, the same rate constants were evaluated via three-dimensional Brownian dynamics simulations. The underlying dynamical theory is an appropriate single- or multiparticle three-dimensional Smoluchowski equation. Taking advantage of approximate geometric symmetries (based on the details of the model channel geometry), well-known formulas for state-to-state transition rates are appealed to herein and adapted as necessary to the problem at hand. Rates of ionic influx from a bulk electrolyte reservoir to the nearest binding site within the channel pore are particularly challenging to compute analytically because they reflect multi-ion interactions (as opposed to single-ion dynamics). A simple empirical correction factor is added to the single-ion rate constant formula in this case to account for the saturation of influx rate constants with increasing bulk Cl(-) concentration. Overall, the agreement between all analytically estimated rate constants is within a factor of 2 of those computed via three-dimensional Brownian dynamics simulations, and often better than this. Current-concentration curves obtained using rate constants derived from these two different computational approaches agree to within 25%.

  4. Use of quartz crystal microbalance to study the effect of chloride, sulphate and magnesium ions on the scaling rate; Apport de la microbalance a quartz dans l'etude de l'influence des ions sulfate, chlorure et magnesium sur la cinetique d'entartrage

    Energy Technology Data Exchange (ETDEWEB)

    Ben Amor, Y.; Triki, E. [Ecole Nationale d' Ingenieurs de Tunis, Unite de Recherche Corrosion et Protection des Metalliques (Tunisia); Bousselmi, I. [Institut National de Recherche Scientifique et Technologique, Lab. des Eaux et Environnement, Hammam-Lif (Tunisia); Sutter, E.; Labbe, J.P.; Fiaud, C. [Universite Pierre et Marie Curie, Lab. de Genie des Procedes Plasmas et Traitements de Surface, 75 - Paris (France)

    2004-07-01

    In this work, an electrochemical quartz crystal microbalance was used to study the effect of chloride, sulphate and magnesium ions on the scaling rate of gold in synthesized water. The chrono-electro-gravimetric results allow the evaluation of the nucleation and crystal growth steps. Infrared analysis of deposits was used to interpret the kinetic data, particularly in SO{sub 4}{sup 2-} and Mg{sup 2+} containing. Threshold effects were identified in each situation and essentially attributed to adsorption phenomena of ions on the metal and/or on the scale layers, as indicated by the influence of electrode potential and concentration of ions in solutions. (authors)

  5. 海洋环境要素综合影响下混凝土中氯离子的传输模型%Chloride Ion Transport Model in Concrete Under Combined Influence of Marine Environment Factors

    Institute of Scientific and Technical Information of China (English)

    练继建; 张杰; 吴慕丹; 王海军

    2016-01-01

    In order to clarify the various marine environment factors that affect the chloride ion erosion,by means of analyzing chloride ion erosion mechanism in reinforced concrete,chloride ion transport calculation model under the marine environment including sunshine,tide and temperature was established. Based on the convection-diffusion transmission model,this model was applied to dynamically coupling calculation of temperature field,humidity field and chlorine ion concentration field in the whole life cycle of concrete structures using finite difference method. In the model,the ASHRAE model was plugged in,and the differencesof moisture diffusion and physical field boundary conditions in dry-wet process caused by tidal water level cycles were considered. The ratio of chloride ion to pore fluid was taken as concentration index. The calculated results of every module were validated by test data,and showed good agreement. The model may provide valuable references for marine concrete durability design.%为澄清多种海洋环境要素对混凝土氯离子侵蚀的综合影响,在对混凝土氯离子侵蚀机理分析的基础上,建立了日照、潮汐、气温等海洋环境综合影响下的混凝土氯离子传输计算模型.该模型在传统对流-扩散模型中增加了ASHRAE晴空日照模型,并考虑了潮汐水位的周期变化导致的干湿两个过程中水分扩散以及水-土界面扩散等边界条件的差异,采取氯离子相对孔隙液的浓度作为控制指标,运用有限差分法,对海上混凝土结构全生命周期内的温度场、湿度场、氯离子浓度场进行动态耦合计算.通过试验实测数据对各模块计算结果进行验证,吻合良好.该模型对于海工混凝土的耐久性设计具有参考价值.

  6. 硫铝酸盐水泥混凝土抗氯离子侵蚀机理分析%Analysis of Mechanism of Resistance to Chloride Ion Erosion of Sulphoaluminate Cement Concrete

    Institute of Scientific and Technical Information of China (English)

    赵军; 蔡高创; 高丹盈

    2011-01-01

    采用欧洲BUILD492《非稳态氯离子迁移试验法》测定普通硅酸盐水泥与硫铝酸盐水泥混凝土的氯离子非稳态扩散系数,应用X射线衍射分析(XRD)、扫描电镜分析(SEM)以及孔结构分析分别对这种水泥水化产物和水泥石内部结构进行研究,并对其抗氯离子侵蚀性能及其抵抗机理进行了研究分析.结果表明:硫铝酸盐水泥是提高混凝土抗氯盐侵蚀性能的一种理想胶凝材料.随着水灰比的降低,硫铝酸盐水泥的抗氯离子侵蚀能力逐渐增强.%For measuring chloride diffusion coefficient of Portland cement concrete and sulphoaluminate cement-based concrete, the method of chloride migration coefficient from non-steady-state experiments is a-dopted. And their cement hydration products and internal structure were researched by the application of X-ray diffraction analysis(XRD) and scanning electron microscopy analysis(SEM). According to the above studies, the resistance to chloride ion erosion of sulphoaluminate cement and the resistance mechanism of the cement were analyzed. The results show that sulphoaluminate cement is an ideal cementitious material which can significantly improve the resistance to chloride ion erosion of the concrete. At the same time, the performance of the cement is gradually improved with the lower water-cement ratio.

  7. Surface Chloride Concentration of Concrete under Shallow Immersion Conditions

    OpenAIRE

    Jun Liu; Kaifeng Tang; Dong Pan; Zongru Lei; Weilun Wang; Feng Xing

    2014-01-01

    Deposition of chloride ions in the surface layer of concrete is investigated in this study. In real concrete structure, chloride ions from the service environment can penetrate into concrete and deposit in the surface layer, to form the boundary condition for further diffusion towards the interior. The deposit amount of chloride ions in the surface layer is normally a function of time, rather than a constant. In the experimental investigation, concrete specimens with different mix proportions...

  8. Green process to recover magnesium chloride from residue solution of potassium chloride production plant

    Institute of Scientific and Technical Information of China (English)

    Lin WANG; Yunliang HE; Yanfei WANG; Ying BAO; Jingkang WANG

    2008-01-01

    The green process to recover magnesium chlor-ide from the residue solution of a potassium chloride pro-duction plant, which comes from the leach solution of a potash mine in Laos, is designed and optimized. The res-idue solution contains magnesium chloride above 25 wt-%, potassium chloride and sodium chloride together below 5 wt-% and a few other ions such as Br-, SO2-4and Ca2+. The recovery process contains two steps: the previous impurity removal operation and the two-stage evapora-tion-cooling crystallization procedure to produce magnes-ium chloride. The crystallized impurity carnallite obtained from the first step is recycled to the potassium chloride plant to recover the potassium salt. The developed process is a zero discharge one and thus fulfills the requirements for green chemical industrial production. The produced magnesium chloride is up to industrial criteria.

  9. 锂渣钢渣复合高性能混凝土抗氯离子的渗透性能%The Permeability of Resistance to Chloride Ion of High Performance Concrete with Lithium Slag and Steel Slag

    Institute of Scientific and Technical Information of China (English)

    吴福飞; 侍克斌; 努尔开力·依孜特罗甫; 董双快; 胡全

    2012-01-01

    为了提高混凝土抗氯离子渗透能力,在混凝土中掺入具有火山灰性的锂渣和会产生自身水化的钢渣.采用正交设计,通过RCM法测试表明,随着锂渣和钢渣掺入总量的增加,混凝土抗氯离子渗透的能力呈现先增大后减小趋势,以锂渣掺量为25%和钢渣掺量为20%时为最优掺量.在水泥水化后,锂渣参与了二次反应,细化了混凝土界面结构,同时促进了钢渣和水泥的相互水化程度,提高了混凝土抗氯离子渗透的能力.%In order to increase permeability of resistance to chloride ion of high performance concrete,the lithium slag with volcanic ash usability and steel slag producing their own hydration were mixed with the concrete. Using orthogonal design, RCM method tests showed that with the incorporation of lithium slag and steel slag increase in the total,concrete resistant to chloride ion penetration ability first increases and then decreases. Lithium slag dosage for 25% and 20% steel slag was regarded as the optimal dosage. After cement hydration,Lithium slag participated in a secondary reaction,the interface structure of concrete was refined,at the same time the mutual degree of hydration of the steel slag and cement was promoted,the a-bility of concrete resistance to chloride ion penetration was improved.

  10. Uses of complexone III and ion exchange resins in colorimetric determination with o-phenanthroline of Fe traces in uranium compounds; Aplicacion de la complexona III y resinas combadoras a la determinacion colorimetrica con orto-fenantro-lina de trazas de dhierro en compuesto de uranio

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez Cellini, R.; Ruiz Sanchez, F.

    1956-07-01

    The determination of small quantities of iron using o-phenanthroline, assumes the elimination of some cations interference by means of pH control before the formation of a coloured complex. We have eluded that difficulty by the connected action of complexones III and ion exchange. the previous forms quelate with the iron (III) with a stability constant high enough to permit the pass of an iron solution through a cation resin column without being fixed which never occurs with the interferer cations. Mercury is the only element with a similar stability, but it has been eliminated previously. (Author) 16 refs.

  11. Chloride : The queen of electrolytes?

    NARCIS (Netherlands)

    Berend, Kenrick; van Hulsteijn, Leonard Hendrik; Gans, Rijk O. B.

    2012-01-01

    Background: Channelopathies, defined as diseases that are caused by mutations in genes encoding ion channels, are associated with a wide variety of symptoms and have been documented extensively over the past decade. In contrast, despite the important role of chloride in serum, textbooks in general d

  12. 持续压荷载作用下混凝土抗氯离子渗透规律研究%Penetration law research of concrete resistance to chloride ion under continuous pressure load

    Institute of Scientific and Technical Information of China (English)

    李维红; 许颖颖; 林川

    2015-01-01

    This paper studies the influence law of permeability of chloride ion in concrete of experi-ment time, load level, curing condition under the sustained pressure load, which is through natural diffusion method. Experiment results show that with the extension of the test time, chloride ion per-meability increases,penetration rate slows. As the load level increases, there is a tendency of the chloride ion content after the first increase and then decrease, the turning point in the middle re-mains to be further studied. The content of chloride ion of test blocks which are cured in calcium hy-droxide solutiong is greater than that cured in constant temperature and humidity box under the same conditions. The research results have a certain significance for concrete durability design and life prediction in Multi-factor coupling conditions.%通过自然扩散法研究了在持续压荷载作用下试验时间、荷载等级、养护条件对混凝土中氯离子渗透规律的影响。试验结果表明:在一定时间段内,随着试验时间的延长,氯离子渗透能力增加,渗透速度减慢;随着荷载等级的增大,氯离子含量有先增大后减小的趋势,对于中间转折点的确定还有待进一步研究;氢氧化钙溶液中养护的试块与恒温恒湿养护箱养护的试块同等条件下相比氯离子含量更大。该研究结果对处于多因素耦合环境中的混凝土耐久性设计及寿命预测具有一定指导意义。

  13. On the Nature of the Intermediates and the Role of Chloride Ions in Pd-Catalyzed Allylic Alkylations: Added Insight from Density Functional Theory

    DEFF Research Database (Denmark)

    Fristrup, Peter; Ahlquist, Mårten Sten Gösta; Tanner, David Ackland

    2008-01-01

    The reactivity of intermediates in palladium-catalyzed allylic alkylation was investigated using DFT (B3LYP) calculations including a PB-SCRF solvation model. In the presence of both phosphine and chloride ligands, the allyl intermediate is in equilibrium between a cationic eta(3)-allylPd complex...... with two phosphine ligands, the corresponding neutral complex with one phosphine and one chloride ligand, and a neutral eta(1)-allylPd complex with one chloride and two phosphine ligands. The eta(1)-complex is unreactive toward nucleophiles. The cationic eta(3)-complex is the intermediate most frequently...... invoked in the title reaction, but in the presence of halides, the neutral, unsymmetrically substituted eta(3)-CoMplex will be formed rapidly from anionic Pd(0) complexes in solution. Since the latter will prefer both leaving group ionization and reaction with nucleophiles in the position trans...

  14. Determination of Sodium Chloride Content in Food(Ion chromatography)%食品中氯化钠含量的测定(离子色谱法)

    Institute of Scientific and Technical Information of China (English)

    刘庆

    2012-01-01

    Level of sodium chloride content in food was analyzed by using ion chromatography for the determination of anions in liquid sample.3.2mM Na_2CO_3+1.0mM NaHCO_3 were adopted as eluent solution,20~80mmol/L H_2SO_4 were adopted as suppression solution.Results showed that the detection limit of sodium chloride was 0.01%,the recovery was 95%.The method shows convenience,high accuracy,easy pretreatment,and can satisfy the analysis for sodium chloride in food.%利用离子色谱法测定样液中的阴离子含量,以3.2mM Na_2CO_3+1.0mM NaHCO_3为淋洗液,以20~80mmol/LH_2SO_4为抑制液,分析测定了食品中氯化钠的含量。结果表明,食品中氯化钠的检出限为0.01%,回收率达95%。该方法简便、快速、准确度高、前处理简单、能够满足食品中氯化钠的分析要求。

  15. MAPbI2.9-xBrxCl0.1 hybrid halide perovskites: Shedding light on the effect of chloride and bromide ions on structural and photoluminescence properties

    Science.gov (United States)

    Atourki, Lahoucine; Vega, Erika; Marí, Bernabé; Mollar, Miguel; Ait Ahsaine, Hassan; Bouabid, Khalid; Ihlal, Ahmed

    2016-12-01

    The optical and structural properties of CH3NH3PbI3 can be adjusted by introducing other extrinsic ions such as chloride and bromide. In this work, mixed bromide iodide lead perovskites with a 10% fraction of chloride were prepared from methylamine, lead nitrate and the corresponding hydro acid (X = I, Br, Cl). The effect of bromide and chloride incorporation on different properties of perovskite thin film was investigated. The Pawley fit method indicates the formation of the iodide halide MAPbI3 Pm-3 m cubic phase for x = 0 and the tetragonal P4/mmm phase for x ≥ 0.3. All deposited films showed a strong absorbance in the UV-vis range. The band gap values were estimated from absorbance measurements. It was found that the onset of the absorption edge for MAPbI2.9-xBrxCl0.1 thin film perovskites ranges between 1.60 and 1.80 eV. Moreover, it was found that both Cl and Br affect the PL emission of the mixed halide lead perovskite, the MAPbI2.9-xBrxCl0.1 films displayed intermediate values from 730 nm (MAPbI2.2Br0.7Cl0.1) to 770 nm (MAPbI2.6Br0.3Cl0.1).

  16. Chloride binding site of neurotransmitter sodium symporters

    DEFF Research Database (Denmark)

    Kantcheva, Adriana Krassimirova; Quick, Matthias; Shi, Lei

    2013-01-01

    Neurotransmitter:sodium symporters (NSSs) play a critical role in signaling by reuptake of neurotransmitters. Eukaryotic NSSs are chloride-dependent, whereas prokaryotic NSS homologs like LeuT are chloride-independent but contain an acidic residue (Glu290 in LeuT) at a site where eukaryotic NSSs...... have a serine. The LeuT-E290S mutant displays chloride-dependent activity. We show that, in LeuT-E290S cocrystallized with bromide or chloride, the anion is coordinated by side chain hydroxyls from Tyr47, Ser290, and Thr254 and the side chain amide of Gln250. The bound anion and the nearby sodium ion...

  17. Correlation Research of Concrete Chloride Ion Binding between Exposure and Wet-dry Cycle%干湿循环和暴露对混凝土氯离子结合能力相关性研究

    Institute of Scientific and Technical Information of China (English)

    张立明; 李长成; 何忠茂

    2014-01-01

    Concrete corrosion tests under longterm immersion and field exposure enviroment were done .The concrete samples total and free chloride ion concentration were measured at different depth under different enviroment .With use of regression method , the relationship between dif-fusion depths or concrete compressive strengths and chloride bind capacity correlation under immersion and exposure .The result shows that:Chloride bind capacity correlation decreased at a exponential function type with the increase of diffusion depthsandconcrete compressive strengths .Predoca-tion of field structure bind capacity at different depths utilize the result of longterm immersion chloride bind capacity through the research result .%进行了盐湖现场暴露和干湿循环环境下钢筋混凝土梁腐蚀试验,分别测定了不同试验环境下钢筋混凝土梁在不同深度的总氯离子浓度和自由氯离子浓度,运用回归分析干湿循环和盐湖现场暴露环境下混凝土氯离子结合能力的相关性系数K与扩散深度、混凝土抗强度的关系。结果表明:随着氯离子扩散深度和混凝土的抗压强度的增加,氯离子结合能力相关性系数K呈指数函数形式递减,研究成果可用于利用干湿循环测定的氯离子结合能力来预测实体结构不同深度内的氯离子结合能力。

  18. 橡胶混凝土抗氯离子渗透性能试验研究%EXPERIMENTAL STUDY ON CHLORIDE IONS PENETRATION RESISTANCE PROPERTIES OF CONCRETE CONTAINING SCRAP RUBBER POWDER

    Institute of Scientific and Technical Information of China (English)

    王宝民; 涂妮; 郭志强

    2012-01-01

    The previous results of our research group show that putting scrap rubber powders into cement concrete can greatly enhance frost resistance. The effect of rubber powders is equal to adding air-entraining mixture, under the condition of right size and quantity. This paper which based on the previous studies continue to research the chloride ions penetration resistance property of rubberized concrete based on RCM and NEL method, the influence of water cement ratio, content and size of rubber powder on chloride ions diffusion coefficient of rubberized concrete is researched. Contrastive analysis about two different testing methods for resistance of concrete to chloride penetration is conducted as well. The results show that there is a correlation between two methods.%前期研究成果显示80~120目废旧轮胎橡胶颗粒掺加到水泥混凝土中,能起到“固体引气剂”的作用,可以大大提高混凝土的抗冻耐久性,适当的粒径和掺加搅拌工艺下,可以替代引气剂使用.文中基于前期研究基础上,采用RCM法和NEL法对橡胶混凝土的抗氯离子侵蚀性能进行研究,研究了水灰比、橡胶粉掺量及粒径对混凝土氯离子扩散系数的影响规律.同时文中对两种不同的抗氯离子渗透性能试验方法也进行了对比分析,结果表明两者之间具有较好的相关性.

  19. 改性偏高岭土复合粉煤灰对混凝土抗渗性能的影响%Effect of Modified Metakaolin and Fly Ash on Permeability of Concrete Resistance to Chloride Ion

    Institute of Scientific and Technical Information of China (English)

    水中和; 王康; 陈伟; 孔贇

    2012-01-01

    将经改性的偏高岭土(MMK)与超细粉煤灰(FA)复合,以低于10%的总掺量内掺到混凝土中,研究了掺入前后和不同掺量对混凝土的工作性能、力学性能、电通量和氯离子扩散系数的影响.并运用压汞、TG-DSC耦合分析和SEM照片等方法,对其影响机理进行了探讨.结果表明:低掺量改性偏高岭土复合粉煤灰对混凝土抗氯离子渗透性能有显著的改善;对混凝土工作性能影响较小,能提高混凝土各龄期抗压强度;可以优化混凝土的孔结构和水泥石-集科界面过渡区.%The effect of modified metakaolin ( MMK) blended with fine fly ash (FA) on permeability of concrete resistance to chloride ion, where the content of MMK and FA mixture was below 10% by weight, has been investigated. Mercury intrusion, TG-DSC analysis and SEM were used to study the mechanism. The collapsed slump, compressive strength, electric flux and chloride diffusion coefficient of concrete mixes containing four different mixtures were tested. The experimental results show that the permeability resistance to chloride ion of concrete significantly increases with the incorporation of MMK and FA mixtures. MMK and FA mixtures have minor effect on the collapsed slump of concrete, while they improve the compressive strength at 3 d, 7 d and 28 d. Also MMK and FA mixtures modify the pore structure and optimize the interfacial transition zone(ITZ).

  20. Effect of the chloride ions on the hydrolysis of praseodymium in a 2M ion force media; Efecto de los iones cloruro sobre la hidrolisis del praseodimio en medio de fuerza ionica 2M

    Energy Technology Data Exchange (ETDEWEB)

    Lopez G, H.; Jimenez R, M.; Solache R, M.; Rojas H, A. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)

    2004-07-01

    The constants of the product of solubility and the first of hydrolysis were determined of the Praseodymium in media 2M of NaClO{sub 4} and 2M of NaCl, to 303 K and under conditions free of CO{sub 2}. The diagram of solubility was obtained (pPr{sub (ac)} - pC{sub H}), by means of a radiochemical method and with it was established the pC{sub H} that limit the saturation and non saturation areas; that diagram allowed, also, to calculate the constant of the product of solubility. Also, it was adjusted with the polynomial of solubility equation, that it allowed to determine and to check the values of the constants of the product of solubility and the first of hydrolysis. Independently, it was determined the first constant of hydrolysis of the element, by means of potentiometric titrations whose data were treated with the computer program named SUPERQUAD and with the adjustment of the equation of the average number of bonds. It was also calculates the log constant {beta}{sub Pr,Cl} of the specie PrCI{sup 2+} starting from the hydrolysis constants obtained in the perchlorate and chloride media. (Author)

  1. Tribenzylammonium chloride

    Directory of Open Access Journals (Sweden)

    Waly Diallo

    2014-05-01

    Full Text Available Single crystals of the title salt, C21H21NH+·Cl−, were isolated as a side product from the reaction involving [(C6H5CH23NH]2[HPO4] and Sn(CH33Cl in ethanol. Both the cation and the anion are situated on a threefold rotation axis. The central N atom in the cation has a slightly distorted tetrahedral environment, with angles ranging from 107.7 to 111.16 (10°. In the crystal, the tribenzylammonium cations and chloride anions are linked through N—H...Cl and C—H...Cl hydrogen bonds, leading to the formation of infinite chains along [001]. The crystal studied was a merohedral twin.

  2. 多尺度预测氯离子在硬化水泥浆体中的有效扩散系数%A multi-scale prediction of effective diffusion coefficient of chloride ion in hardened cement paste

    Institute of Scientific and Technical Information of China (English)

    孙国文; 孙伟; 张云升; 刘志勇

    2011-01-01

    基于水泥水化形成的复杂微结构特征,将硬化水泥浆体由下至上划分为3个不同的尺度,分别为C-S-H凝胶、水泥水化产物和硬化水泥骨架;各尺度上采用不同均匀化方法来预测氯离子的扩散系数,同时在各尺度上所考虑的夹杂均视为球形,其中低尺度的输出参数作为较高尺度的输入参数,这样根据多尺度过渡理论,逐尺度地将硬化水泥浆体的微结构与氯离子的传输行为建立定量关系.对水灰质量比分别为0 23,0.25和0.53的硬化水泥浆体,采用RCM法测定其氯离子扩散系数,来验证所提预测方法,并用文献值进一步验证.研究表明:预测的氯离子扩散系数与实测结果吻合很好,验证了不同尺度上需采用不同均匀化方法的合理性.%Based on the complex microstruclure with a multi-scale pore structure formed from the initial cement grains hydrate, the hardened cement paste was characterized into three-scale from down to up, C - S - H gel, hydrated products of cement and skeleton of hardened cement paste. Different homogeni-zation models were used to predict diffusion coefficient of chloride ion and all inclusions were considered as sphere at different scale. According to multi-scale transition theory, (he output parameters of low scale were considered as input parameters of higher scale. Based on the multi-scale transition theory, the quantitative relationship between the mierostructure of hardened cement paste and macroscopic transport behavior oi chloride ion in hardened cement paste was built for different scales one by one. By rapid chloride migration method, the diffusion coefficient of chloride ion was measured for the hardened cement paste with different ratio of water to cement of 0. 23 , 0. 25 and 0. 53. The proposed prediction was verified by the measured diffusion coefficient and reported value. The results show that predicted values of diffusion coefficient of chloride ion are consistent with

  3. Influence of Mineral Admixture on Anti-chloride Ion Permeability of Recycled Aggregate Concrete%矿物掺和料对再生混凝土抗氯离子渗透性能的影响研究

    Institute of Scientific and Technical Information of China (English)

    罗伯光; 覃荷瑛

    2014-01-01

    Some recycled concrete specimens with different water to binder ratio are analyzed by experiments in order to study on the influence of the mineral admixture on anti-chloride ion permeability of recycled aggregate concrete by accelerated chloride migration test.The results show that the diffusion coefficient of chloride ion of recycled concrete with 8% silica fume has lower 12.2%~53.4% than that of them not with the mineral admixture,with 25% fly ash has lower 7.8%~50. 1% and with 25% slag has lower 7. 1%~43.9%.We can see that three kinds of mineral admixtures can all enhance anti-chlo-ride ion permeability of recycled aggregate concrete,silica fume has the best effect,slag is in the second place,and fly ash is in the third place.%试验设计制作了几组掺有不同矿物掺和料、不同配合比的再生混凝土试块,利用加速氯离子渗透性试验对试块进行了抗氯离子渗透性能的测定,以考察常用矿物掺和料对再生混凝土抗氯离子渗透性能的影响规律。试验结果表明,掺有8%硅灰的再生混凝土试块,其氯离子渗透系数减少12.2%~53.4%;掺有25%的粉煤灰,再生混凝土试块氯离子渗透系数减少7.8%~50.1%;掺有25%矿渣微粉的再生混凝土试块,其氯离子渗透系数减少7.1%~43.9%;可见3种矿物掺和料-粉煤灰、矿渣微粉以及硅灰对再生混凝土的抗氯离子渗透性能均有一定的提高,其中以硅粉的效果最好,粉煤灰次之,矿渣微粉较差。

  4. Theoretical Study on the Geometrical and Electronic Structures of Choline Chloride Ion Pair%氯化胆碱离子对几何及电子结构的量子化学研究

    Institute of Scientific and Technical Information of China (English)

    劳旺梅; 孙慧

    2013-01-01

    采用密度泛函理论方法,在B3 LYP/6-31G(d,p)水平上研究氯化胆碱离子对的几何与电子结构.共有四种稳定离子对构型被发现.在稳定离子对结构中,Cl-离子倾向与阳离子形成多重稳定氢键.阴阳离子间的氢键相互作用主要通过Cl-离子的LPcl轨道和阳离子的σC-H*,或σC-H*轨道间的相互作用完成.研究发现这种σ相互作用很弱,由此判断阴阳离子间大的相互作用能并不是单纯的氢键作用能,还包含阴阳离子间静电作用能的贡献;而且是主要贡献.阴阳离子间大的相互作用能还为氯化胆碱的高熔点提供了解释.%The geometrical and electronic structures of choline chloride ion pair have been studied by performing density functional theory calculations on the B3LYP/6-31G(d,p) level. Four stable configurations for choline chloride ion pair have been obtained. It is found that there exist multiply hydrogen bonds between cation and Cl-anion. The intrinsic hydrogen bond interaction between the cation and Cl- anion mainly occurs between one LPC1 of Cl- anion and the σ*C-H or σ*O-H orbitals of the cation moiety. However, the σ-type interactions are weak. Therefore, it is considered that ion pair is highly stable owing to not only the multiple hydrogen bond interactions, but also the strong electrostatic attraction. The large interaction energy between the cation and Cl- anion may be responsible for the higher melting point of choline chloride.

  5. 矿物掺合料对自密实混凝土抗氯离子渗透性的影响%Influence of Mineral Admixtures on the Resistance to Penetration of Chloride Ion in Self-compacting Concrete

    Institute of Scientific and Technical Information of China (English)

    张长清; 吴海兵; 杜明月; 刘齐霞; 郑力翀; 何广利; 徐文胜

    2012-01-01

    Durability is an important property for self - compacting concrete ( SCC). This paper studied the resistance to chloride ion penetration performance of SCC with addition of fly ash and slag based on concrete coulomb electric flux test. Both fly ash and slag can improve the resistance to chloride ion permeability in SCC and slag shows better effect than fly ash. The addition of both fly ash and slag show little effect on the resistance to chloride ion permeability in SCC. The mechanism is that the addition of fly ash or slag can improve the density of cement paste and reinforce the interfacial transition zone between cement paste and aggregate. Both physical and chemical adsorption of Cl on the mineral admixtures contributes to the consolidation of Cl and the reduction of Cl permeability. The mineral admixtures can decrease the risk of segregation and bleeding in SCC. Fly ash is more effective than the slag powder for improving SCC fluidity. The addition of both slag and fly ash shows an enhanced effect on the SCC strength gain and SCC strength grade at 28 d can be increased from 5 Mpa to 10 Mpa.%耐久性是自密实混凝土(SCC)的重要性质.本文应用电通量法研究了掺粉煤灰、矿渣的SCC抗氯离子渗透性能,通过对单掺和复掺时SCC电通大小的分析发现:粉煤灰和矿渣都能改善SCC的抗氯离子渗透性能,矿渣提高SCC的抗氯离子渗透性能要优于粉煤灰,二者复掺对SCC抗氯离子渗透的复合叠加效应并不明显.其机理是粉煤灰和矿渣提高水泥石密实性,强化混凝土界面过渡区,粉煤灰、矿渣物理化学吸附作用能固结Cl-,降低Cl-渗透性.SCC中掺入掺合料能减少离析、避免泌水,达到自密实效果,粉煤灰对混凝土流动增大的作用效果要优于磨细矿渣的效果.掺合料复掺对自密实混凝土强度具有复合叠加效应,混凝土28 d强度等级可提高1~2级.

  6. Determination of Chloride and Sulfate in Lithium Carbonate Crude Drug by Ion Chromatography%离子色谱法测定碳酸锂原料药中的氯化物及硫酸盐

    Institute of Scientific and Technical Information of China (English)

    徐桂连; 耿欣

    2015-01-01

    目的::建立抑制离子色谱法测定碳酸锂原料药中氯化物及硫酸盐的含量。方法:用Thermo IonPac AS11(250 mm ×4 mm)阴离子交换柱和IonPac AG 11(50 mm ×4 mm)保护柱,淋洗液为10 mmol·L-1氢氧化钾溶液,由自动淋洗液发生器产生,流速为1.0 ml·min-1,柱温30℃,电导池温度35℃,阴离子抑制器抑制器电流36 mA,进样量10μl。结果:氯离子及硫酸根离子在1.0~20μg·ml-1范围内线性关系良好(r分别为0.9951,0.9973),氯离子回收率为106.6%(RSD=2.6%,n=6),硫酸根离子回收率为100.3%(RSD=1.9%,n=6)。结论:该方法准确可靠,可用于碳酸锂原料药中氯化物及硫酸盐的测定。%Objective:To establish a method for the determination of chloride and sulfate in lithium carbonate crude drug by sup-pressed ion chromatography. Methods:The analysis column and the guard column was Thermo IonPac AS11(250 mm × 4 mm) and IonPac AG 11(50 mm ×4 mm), respectively. Potassium hydroxide solution(10 mmol·L-1) generated by an eluent generator(EG) was used as the eluent at a flow rate of 1. 0 ml·min-1 . And the temperature of column and conductivity cell was 30℃ and 35℃, re-spectively. The suppressor electric current was 36 mA, and the injection volume was 10 μl. Results:The linear range of chloride ion and sulfate ion was 1. 0-20μg·ml-1 with r of 0. 995 1 and 0. 997 3,respectively, and the recovery was 106. 6%(RSD=2. 6%,n=6) and 100. 3%(RSD=1. 9%,n=6), respectively. Conclusion:The method is accurate and reliable, and can be used in the determina-tion of chloride and sulfate in lithium carbonate crude drug.

  7. Flow-injection potentiometry by poly(vinyl chloride)-membrane electrodes with diphosphoryl-dicarboxylicacid-p-tert-butylcalix[4]arene ionophore for the determination of Th(IV) ions.

    Science.gov (United States)

    Mizani, Farhang; Shamsipur, Mojtaba; Yaftian, Mohammad R; Matt, Dominique

    2013-01-01

    A new coated ion-selective electrode for the determination of trace thorium ions by flow-injection potentiometry (FIP) has been developed. A poly(vinyl chloride) (PVC)-based membrane was coated on a graphite electrode. The optimum membrane contained 5 wt% diphosphoryl-dicarboxylicacid-p-tert-butylcalix[4]arene (L) as the ionophore, 59 wt% dioctyl phthalate (DOP), 33 wt% PVC and 3 wt% additive sodium tetraphenylborate. The response was linear from 2.0 × 10(-7) to 1.0 × 10(-2) M with a slope of 13.9 mV decade(-1) and a limit of detection of 9.0 × 10(-8) M. The pH-independent region ranged from 3.15 to 6.5, and the lifetime was longer than 8 weeks when used in the flow injection analysis (FIA) system. Selectivity coefficients for several ions were obtained by the separate solutions method. Results showed that, for all cations used, the selectivity coefficients were in the order of 10(-3), or smaller. The flow cell is simple to construct and free from memory effect problems over long periods of use. The proposed sensor was successfully applied to the direct determination of thorium in both real and synthetic samples.

  8. Uranyl complexation by chloride ions. Formation of a tetrachlorouranium(VI) complex in room temperature ionic liquids [Bmim][Tf2N] and [MeBu3N][Tf2N].

    Science.gov (United States)

    Sornein, M-O; Cannes, C; Le Naour, C; Lagarde, G; Simoni, E; Berthet, J-C

    2006-12-25

    The tetrachlorouranium(VI) complex is formed in [Bmim][Tf2N] and [MeBu3N][Tf2N] from a uranium(VI) solution in the presence of a stoichiometric quantity of chloride ions. The [UVIO2Cl4]2- absorption and emission spectra show bands splitting in comparison with the [UVIO2]2+ spectra, as observed in the solid state, organic solvents, and chloroaluminate-based ionic liquids. The fluorescence lifetime of [UO2Cl4]2- in [MeBu3N][Tf2N] is 0.7 +/- 0.1 mus. The reduction potential of this complex is -1.44 and -1.8 V vs Ag/Ag+ respectively in [Bmim][Tf2N] and [MeBu3N][Tf2N] and does not depend on the chloride concentration. The mechanism proposed for the redox process is a monoelectronic reduction to form [UVO2Cl4]3-, followed by a chemical reaction. The tetrachlorouranium(V) complex seems more stable in [Bmim][Tf2N] than in [MeBu3N][Tf2N]. The electrochemical analysis put in evidence specific interactions of the ionic liquid cation with the uranium anionic species.

  9. Determination of bromide, chloride, fluoride, nitrate and sulphate by ion chromatography: comparisons of methodologies for rainfall, cloud water and river waters at the Plynlimon catchments of mid-Wales

    Directory of Open Access Journals (Sweden)

    2007-01-01

    Full Text Available The results of determination of bromide, chloride, fluoride, nitrate and sulphate using ion chromatography (IC are compared with those obtained by colorimetric and inductively coupled plasma optical emission spectroscopy (ICPOES for rainfall, cloud water and stream waters in the Plynlimon experimental catchments of mid-Wales. For bromide, the concentrations determined by IC are lower than those for the colorimetric method used; the colorimetric method probably determined bromide plus organo-bromine compounds. It is suggested that the values determined by the colorimetric method be termed dissolved labile bromine (DLBr. The study shows that sulphate is the overriding form of sulphur in the waters. For chloride and nitrate, measurements by both methods approach a 1:1 relationship that is barely statistically significantly different from unity. For fluoride, the IC method gives lower values than the colorimetric, especially for the stream waters. However, the colorimetric method determines total fluorine so that a difference is to be expected (for example, fluoride strongly complexes with aluminium that is present, especially in the streamwater.

  10. Formation of an Ion-Pair Molecule with a Single NH+...Cl- Hydrogen Bond: Raman spectra of 1,1,3,3-Tetramethylguanidinium chloride in the solid state, in solution and in the vapor phase

    DEFF Research Database (Denmark)

    Berg, Rolf W.; Riisager, Anders; Fehrmann, Rasmus

    2008-01-01

    Some ionic compounds (salts) form liquids when heated to temperatures in the range of 200-300 °C. They may be referred to as moderate temperature ionic liquids. An example of such a compound is the 1,1,3,3- tetramethylguanidinium chloride, [TMGH]Cl, melting at ∼212 °C. The chemistry....... It was discovered that the compound can be easily sublimed by heating to about 200-230 °C. In the Raman spectrum of the vapor at 225 °C, a characteristic strong band at 2229 cm-1 was found and interpreted to show that the gas phase consists of monomeric ion-pair “molecules” held together by a single N-H+ · · · Cl...

  11. 氯化钠对锂离子电池石墨负极的修饰改性%Modification of Graphite Anode for Li-ion Batteries by Sodium Chloride

    Institute of Scientific and Technical Information of China (English)

    周友元; 李新海; 郭华军; 王志兴; 杨勇; 朱文明

    2007-01-01

    The electrochemical performance of a graphite electrode for rechargeable lithium-ion batteries was improved by pretreatment of graphite powders with NaCl aqueous solutions. The procedure of the pretreatment was simple and easy. Graphite powders were dispersed in the aqueous solutions of sodium chloride, followed by stirring, heating and drying. The irreversible capacity at the initial cycle was suppressed by the modification. The sample modified with 1% NaCl had the best electrochemical performances with a reversible capacity of 364.8mAh·g-1, an irreversible capacity of 47.4 mAh·g-1, and an initial coulombic efficiency of 88.5%. The cycling stability of the Li/C cells with modified graphite as anodes was improved. The capacity retention ratio at the 30th cycle was up to 91.97%.

  12. An insight into the passivation of cupronickel alloys in chloride environment

    Indian Academy of Sciences (India)

    J Mathiyarasu; N Palaniswamy; V S Muralidharan

    2001-02-01

    Cupronickels offer enhanced corrosion protection in marine environments by the formation of passive films on the surface. Cyclic voltammetric studies were carried on cupronickels in chloride solutions at H 6.3 to understand the role of chloride ions in passive film formation. Increase in nickel content of the alloy and of chloride ions in solution decreases film resistance. Chloride ions take part in reduction of the passive film to copper. A solid-state model for passive film formation involving chloride ions has been attempted.

  13. Mass concentration and ion composition of coarse and fine particles in an urban area in Beirut: effect of calcium carbonate on the absorption of nitric and sulfuric acids and the depletion of chloride

    Directory of Open Access Journals (Sweden)

    H. Kouyoumdjian

    2006-01-01

    Full Text Available Levels of coarse (PM10-2.5 and fine (PM2.5 particles were determined between February 2004 and January 2005 in the city of Beirut, Lebanon. While low PM mass concentrations were measured in the rainy season, elevated levels were detected during sand storms originating from Arabian desert and/or Africa. Using ATR-FTIR and IC, it was shown that nitrate, sulfate, carbonate and chloride were the main anionic constituents of the coarse particles, whereas sulfate was mostly predominant in the fine particles in the form of (NH42SO4. Ammonium nitrate was not expected to be important because the medium was defined as ammonium poor. In parallel, the cations Ca2+ and Na+ dominated in the coarse, and NH4+, Ca2+ and Na+ in the fine particles. Coarse nitrate and sulfate ions resulted from the respective reactions of nitric and sulfuric acid with a relatively high amount of calcium carbonate. Both CaCO3 and Ca(NO32 crystals identified by ATR-FTIR in the coarse particles were found to be resistant to soaking in water for 24 h but became water soluble when they were formed in the fine particles suggesting, thereby, different growth and adsorption phenomena. The seasonal variational study showed that nitrate and sulfate ion concentrations increased in the summer due to the enhancement of photochemical reactions which facilitated the conversion of NO2 and SO2 gases into NO3- and SO42-, respectively. While nitrate was mainly due to local heavy traffic, sulfates were due to local and long-range transport phenomena. Using the air mass trajectory HYSPLIT model, it was found that the increase in the sulfate concentration correlated with wind vectors coming from Eastern and Central Europe. Chloride levels, on the other hand, were high when wind originated from the sea and low during sand storms. In addition to sea salt, elevated levels of chloride were also attributed to waste mass burning in proximity to the site. In comparison to other neighboring Mediterranean

  14. Determination of optimal conditions for the synthesis of trilon-B-modified zirconium phosphate (TZP) ion-exchanger from zirconyl chloride

    Energy Technology Data Exchange (ETDEWEB)

    Boichinova, E.S.; Nikolaeva, R.B.; Dragun, O.P.

    1992-07-10

    The dependence of the ion-exchange properties of modified zirconium phosphate (TZP) ion-exchange on pH and time of holding of zirconium(IV) trilonate solution before the addition of the precipitant and also on the acidity of the mother liquor was studied in order to optimize the conditions of synthesis of TZP from zirconium oxychloride. A method for the synthesis of TZP has been developed under conditions optimal for the formation of a product with beads of a fair size and having good kinetic properties. 6 refs., 3 tabs.

  15. Fragmentation of meso-Tetraphenyl iron(III) porphyrin chloride (FeTPPCl) in collisions with Kr{sup 8+} ions

    Energy Technology Data Exchange (ETDEWEB)

    Li, B; Gutierrez, G; Chen, L; Bredy, R; Bernard, J; Montagne, G; Martin, S [Universite de Lyon, Universite Lyon 1, CNRS, LASIM UMR5579, Bat Orion 43 Bd du 11 Novembre 1918, F69622, Villeurbanne (France); Ma, X [Institute of Modern Physic, Chinese Academy of Sciences, Lanzhou 730000 (China); Bernigaud, V; Manil, B; Maunoury, L; Huber, B, E-mail: chen@univ-lyon1.f [CIMAP (CEA-CNRSCaen-UCBN), Bd Henri Becquerel (BP 5133), F-14070 Caen Cedex (France)

    2009-04-01

    Fragmentation of FeTPPCl (C4{sub 4}H{sub 28}N{sub 4}FeCl) induced by Kr{sup 8+} impact at 80 keV has been investigated. Fragmentation schemes have been studied for different charge states of parent ions (r = 1-3). The dominant low-energy-cost fragmentation channel is the emission of neutral chlorine independently to the charge of the molecule. For the monocharged FeTPPCl parent ions, a minor channel corresponding to the emission of a chlorine anion is observed with a measured rate of about 3% +- 1%. For the dication molecule, the evaporation of a neutral phenyl molecule is the dominant channel, whereas for the trication molecule the dominant channel is the asymmetrical fission by emission of a charged phenyl. These processes are discussed in terms of charge distribution of the molecule.

  16. The effect of chloride ions on the corroded surface layer of 00Cr22Ni5Mo3N duplex stainless steel under cavitation.

    Science.gov (United States)

    Wan, Tong; Xiao, Ning; Shen, Hanjie; Yong, Xingyue

    2016-11-01

    The effects of Cl(-) on the corroded surface layer of 00Cr22Ni5Mo3N duplex stainless steel under cavitation in chloride solutions were investigated using nanoindentation in conjunction with XRD and XPS. The results demonstrate that Cl(-) had a strong effect on the nano-mechanical properties of the corroded surface layer under cavitation, and there was a threshold Cl(-) concentration. Furthermore, a close relationship between the nano-mechanical properties and the cavitation corrosion resistance of 00Cr22Ni5Mo3N duplex stainless steel was observed. The degradation of the nano-mechanical properties of the corroded surface layer was accelerated by the synergistic effect between cavitation erosion and corrosion. A key factor was the adsorption of Cl(-), which caused a preferential dissolution of the ferrous oxides in the passive film layer on the corroded surface layer. Cavitation further promoted the preferential dissolution of the ferrous oxides in the passive film layer. Simultaneously, cavitation accelerated the erosion of the ferrite in the corroded surface layer, resulting in the degradation of the nano-mechanical properties of the corroded surface layer on 00Cr22Ni5Mo3N duplex stainless steel under cavitation.

  17. Effect of chloride and sulfate ions in simulated AVT waters on electrochemical corrosion behavior and oxide film characteristics of LP steam turbine materials in power plants

    Energy Technology Data Exchange (ETDEWEB)

    Nakane, Takahiro [Shinshu Univ., Nagano City (Japan). Interdisciplinary Graduate School of Sience and Technology; Goto, Teruyuki [NSK Ltd., Tokyo (Japan); Niu, Li-Bin [Shinshu Univ., Nagano City (Japan). Dept. of Environmental Science and Technology; Takaku, Hiroshi [Shinshu Univ., Nagano City (Japan). Faculty of Engineering

    2010-07-15

    Electrochemical corrosion behavior and film characteristics were investigated in simulated all-volatile treatment (AVT) waters containing both sulfate (SO{sub 4}{sup 2-}) and chloride (Cl{sup -}) for 13Cr, 16Cr-4Ni, 3.5NiCrMoV and high-purity 9CrMoV steels of low-pressure (LP) steam turbines in power plants. Concerning the 13Cr, 16Cr-4Ni and high-purity 9CrMoV steels, the corrosion pit growth proceeded with an increasing content of SO{sub 4}{sup 2-} up to 50 mg x kg{sup -1} in the test water with 100 mg x kg{sup -1} Cl{sup -}, although a SO{sub 4}{sup 2-} concentration above 50 mg x kg{sup -1} in the test water suppressed the corrosion pit growth due to the combined effect of Cl{sup -} and SO{sub 4}{sup 2-}. No corrosion pits occurred for 3.5NiCrMoV steel, which showed predominantly general corrosion in the test waters with Cl{sup -} and SO{sub 4}{sup 2-}. It is concluded that both the heat-treatment-improved 16Cr-4Ni steel for blades and the newly developed high-purity 9CrMoV steel for rotors have a high resistance to pitting corrosion. (orig.)

  18. Novel silicon/carbon nano-branches synthesized by reacting silicon with methyl chloride: A high performing anode material in lithium ion battery

    Science.gov (United States)

    Ren, Wenfeng; Wang, Yanhong; Tan, Qiangqiang; Zhong, Ziyi; Su, Fabing

    2016-11-01

    To overcome the existing technical barriers of pulverization and fast capacity fading of Si/C composite anodes in lithium ion batteries and to low their production cost, we have developed a facile method for preparing Si/C nano-branches (Si/C NBs) by reacting commercial Si microparticles directly with CH3Cl gas over Cu-based catalyst particles followed by a simple post treatment. The samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, and Raman spectroscopy. It was found that the diameter and the length of Si/C NBs were ∼70 nm and ∼6 μm, respectively. When used as the anode materials for lithium ion batteries, they displayed excellent electrochemical properties with an average specific capacity of 849 mA h g-1 at a current density of 50 mA g-1. The much improved electrochemical performance is attributed to the unique branched nanostructure and the coated carbon layer on the surface, which can effectively increase the electrical conductivity and buffer the volume change. This work provides a simple and low-cost route to prepare Si/C anode materials with novel branched nanostructure for lithium ion batteries.

  19. Hexavalent chromium recovery by liquid–liquid extraction with 2-octylaminopyridine from acidic chloride media and its sequential separation from other heavy toxic metal ions

    Directory of Open Access Journals (Sweden)

    C.P. Mane

    2016-11-01

    Full Text Available A systematic study of extraction of chromium(VI with 2-octylaminopyridine (2-OAP in xylene at room temperature has been conducted. Quantitative extraction of chromium(VI was observed in the 0.4–0.8 M concentration range of hydrochloric acid. From the extracted complex species in the organic phase, chromium(VI was back extracted with 7 N ammonia (3 × 10 mL, and was determined by spectrophotometric method. Various parameters such as 2-OAP concentration, equilibrium period, effect of various diluents, aqueous: organic volume ratio, acidity and diverse ions were studied. The extraction reaction proceeds with ion-pair formation and the stoichiometry of extracted species was found to be [(2OAPH+ CrO3Cl−](org. The separation and determination of chromium(VI from associated and toxic metals in binary, ternary and multicomponent mixture were carried out. The method permits the sequential separation of chromium(VI from other toxic metals and has been used to separate and determine chromium(VI from alloys, and effluent water samples from tannery industries.

  20. Surface Chloride Concentration of Concrete under Shallow Immersion Conditions

    Directory of Open Access Journals (Sweden)

    Jun Liu

    2014-09-01

    Full Text Available Deposition of chloride ions in the surface layer of concrete is investigated in this study. In real concrete structure, chloride ions from the service environment can penetrate into concrete and deposit in the surface layer, to form the boundary condition for further diffusion towards the interior. The deposit amount of chloride ions in the surface layer is normally a function of time, rather than a constant. In the experimental investigation, concrete specimens with different mix proportions are immersed in NaCl solution with a mass concentration of 5%, to simulate the shallow immersion condition in sea water, and the surface chloride concentrations are measured at different ages. It is found that the surface chloride concentration increases following the increasing immersion durations, and varies from a weight percentage of 0.161%–0.781% in concretes with different mix proportions. The w/c (water-to-cement ratio influences the surface chloride concentration significantly, and the higher the w/c is, the higher the surface chloride concentration will be, at the same age. However, following the prolonging of immersion duration, the difference in surface chloride concentration induced by w/c becomes smaller and smaller. The incorporation of fly ash leads to higher surface chloride concentration. The phenomena are explained based on pore structure analyses.

  1. Electrodeposition of copper on a Pt(111) electrode in sulfuric acid containing poly(ethylene glycol) and chloride ions as probed by in situ STM.

    Science.gov (United States)

    Fu, YunLin; Pao, Te; Chen, Sih-Zih; Yau, ShuehLin; Dow, Wei-Ping; Lee, Yuh-Lang

    2012-07-03

    This study employed real-time in situ STM imaging to examine the adsorption of PEG molecules on Pt(111) modified by a monolayer of copper adatoms and the subsequent bulk Cu deposition in 1 M H(2)SO(4) + 1 mM CuSO(4)+ 1 mM KCl + 88 μM PEG. At the end of Cu underpotential deposition (~0.35 V vs Ag/AgCl), a highly ordered Pt(111)-(√3 × √7)-Cu + HSO(4)(-) structure was observed in 1 M H(2)SO(4) + 1 mM CuSO(4). This adlattice restructured upon the introduction of poly(ethylene glycol) (PEG, molecular weight 200) and chloride anions. At the onset potential for bulk Cu deposition (~0 V), a Pt(111)-(√3 × √3)R30°-Cu + Cl(-) structure was imaged with a tunneling current of 0.5 nA and a bias voltage of 100 mV. Lowering the tunneling current to 0.2 nA yielded a (4 × 4) structure, presumably because of adsorbed PEG200 molecules. The subsequent nucleation and deposition processes of Cu in solution containing PEG and Cl(-) were examined, revealing the nucleation of 2- to 3-nm-wide CuCl clusters on an atomically smooth Pt(111) surface at overpotentials of less than 50 mV. With larger overpotential (η > 150 mV), Cu deposition seemed to bypass the production of CuCl species, leading to layered Cu deposition, starting preferentially at step defects, followed by lateral growth to cover the entire Pt electrode surface. These processes were observed with both PEG200 and 4000, although the former tended to produce more CuCl nanoclusters. Raising [H(2)SO(4)] to 1 M substantiates the suppressing effect of PEG on Cu deposition. This STM study provided atomic- or molecular-level insight into the effect of PEG additives on the deposition of Cu.

  2. Capillary ion electrophoresis of inorganic anions and uric acid in human saliva using a polyvinyl alcohol coated capillary column and hexamethonium chloride as additive of background electrolyte.

    Science.gov (United States)

    Mori, Masanobu; Yamamoto, Tsukasa; Kaseda, Maki; Yamada, Sachiko; Itabashi, Hideyuki

    2012-03-01

    A combination of polyvinyl alcohol chemically coated capillary (PVA capillary) and background electrolyte (BGE) with ion-pair reagent (hexamethonium dichloride, HMC) was used on capillary ion electrophoresis-UV detection (CIE-UV) for analysis of Br⁻, I⁻, NO₂⁻, NO₃⁻, SCN⁻ and uric acid in human saliva. The PVA capillary prepared in our laboratory minimized electro-osmotic flow (EOF) at the BGE in pH 3-10, and did not affect the UV detection at 210 nm by the PVA-layer on capillary wall. Therefore, use of the PVA capillary was suitable for sensitive UV detection for analyte anions, as well as suppression of protein adsorption. In this study, we optimized the BGE of 10 mM phosphate plus 10 mM HMC with applying a voltage of -15 kV. HMC as an additive to BGE could manipulate the electrophoretic mobility of anions, without electrostatic adsorption to the PVA capillary. The CIE-UV could separate and determine analyte anions in human saliva containing proteins by the direct injection without pretreatments such as dilution or deproteinization within 13 min. The relative standard deviations (n=10) were ranged of 0.5-1.6% in migration times, 2.2-6.8% in peak heights and 2.8-8.4% in peak areas. The limits of detection (S/N=3) were ranged of 3.42-6.87 μM. The peak height of anions in this system was gradually decreased through the successive injections of saliva samples, but the problem was successfully solved by periodically conditioning the PVA capillary. The quantifiability of anions in human saliva samples by the CIE-UV was evaluated through the recoveries by standard addition methods and comparison of other representative analytical methods, as well as identification by ion chromatography (IC). From the anion analyses in 12 different saliva samples, the CIE-UV demonstrated that can obtain obvious differences in concentrations of SCN⁻ between of smoker and non-smoker and those of uric acid between male and female with satisfactory results.

  3. Response to comments on "Local impermeant anions establish the neuronal chloride concentration"

    DEFF Research Database (Denmark)

    Glykys, J; Dzhala, V; Egawa, K

    2014-01-01

    We appreciate the interest in our paper and the opportunity to clarify theoretical and technical aspects describing the influence of Donnan equilibria on neuronal chloride ion (Cl(-)) distributions....

  4. XPS of fast-frozen hematite colloids in NaCl aqueous solutions: I. Evidence for the formation of multiple layers of hydrated sodium and chloride ions induced by the {001} basal plane

    Energy Technology Data Exchange (ETDEWEB)

    Shchukarev, Andrei; Boily, Jean F.; Felmy, Andrew R.

    2007-12-13

    The influence of the {001} basal plane of hematite on the composition of fast-frozen centrifuged wet pastes of hematite prepared at pH 4 and 9 and at ionic strengths of 0, 10 and 100 mM NaCl was investigated by x-ray photoelectron spectroscopy. Two hematite preparations consisted of micrometer-sized platelets with 42% (HEM-1) and 95% (HEM-8) of the surface terminated by the {001} basal plane. A third preparation of spherical shape with no recognizable crystal plane (HEM-control) was used as a control to these experiments. All hematite samples responded to changes in pH and ionic strength, showing that acid/base reactions of surface hydroxyl groups control the composition of the paste. The HEM-1 and HEM-8 sample exhibited divergent properties at the highest ionic strength (100 mM) with energy loss features in the Na 1s and Cl 2p spectra and an important water content. As the spectra were typical of hydrated Na+ and Cl- ions and that the surface concentrations were unusually large, the HEM-1 and HEM-8 samples are proposed to induce the formation of a three-dimensional distribution of these ions in the paste. The sodium, chloride and water content was also correlated to the fraction of the {001} basal plane present in the sample and provided evidence for an approximate stochiometric Na:Cl:H2O ratio of 1:1:2. The {001} basal plane of hematite is consequently proposeD to be the cause of this feature.

  5. Regulated trafficking of the CFTR chloride channel

    NARCIS (Netherlands)

    Braakman, L.J.; Kleizen, B.; Jonge, H.R. de

    2000-01-01

    The cystic fibrosis transmembrane conductance regulator (CFTR), the ABC transporter encoded by the cystic fibrosis gene, is localized in the apical membrane of epithelial cells where it functions as a cyclic AMP-regulated chloride channel and as a regulator of other ion channels and transporters. Wh

  6. Chloride ingress prediction

    DEFF Research Database (Denmark)

    Frederiksen, Jens Mejer; Geiker, Mette Rica

    2008-01-01

    Prediction of chloride ingress into concrete is an important part of durability design of reinforced concrete structures exposed to chloride containing environment. This paper presents the state-of-the art: an analytical model which describes chloride profiles in concrete as function of depth...... makes physical sense for the design engineer, i.e. the achieved chloride diffusion coefficients at 1 year and 100 years, D1 and D100 respectively, and the corresponding achieved chloride concentrations at the exposed concrete surface, C1 and C100. Data from field exposure supports the assumption of time...... dependent surface chloride concentrations and the diffusion coefficients. Model parameters for Portland cement concretes with and without silica fume and fly ash in marine atmospheric and submerged South Scandinavian environment are suggested in a companion paper based on 10 years field exposure data....

  7. The electrochemical behaviour study of La{sup 3+} ion in fused chlorides bath. The LaNi{sub 5} formation; Estudo do comportamento eletroquimico do ion La{sup 3+} em meio a cloretos fundidos. A formacao de LaNi{sub 5}

    Energy Technology Data Exchange (ETDEWEB)

    Dias, Cristiane

    2002-07-01

    The electrochemical behaviour of La{sup 3+} ion was studied in fused chlorides bath, with purpose to obtain LaNi{sub 5} formation parameters. The lanthanum reduction/reoxidation mechanism and intermetallic compound formation were investigated by cyclic voltammetry, chronopotentiommetry and galvanostatic electrodeposition. The electrolyte employed was eutectic mixture NaCl-KCl (1:1) with anhydrous LaCl{sub 3} as solute, since 0,25 mol. L{sup -1} up to 2 mol. L{sup -1}, between 700 deg C and 800 deg C. The anhydrous LaCl{sub 3} was prepared by lanthanum chloride slow dehydration with HCl flow and heating until 300 deg C. Over molybdenum, results depicted that lanthanum electrochemical behaviour was quasi-reversible and electrodeposition occurred in a charge transfer step with three electrons. In nickel, intermetallic compound formation was observed by interdiffusion. The scanning electronic microscopy (SEM-EDS) and X ray diffraction analysis indicated that layers composition depend on temperature and solute concentration in fused bath. Mainly LaNi{sub 5} intermetallic compound was formed with LaCl{sub 3} anhydrous concentration of 2 mol. L{sup -1} at 750 deg C, with cathodic current density until 100 mA.cm{sup -2}. (author)

  8. Improved methods for Feynman path integral calculations of vibrational-rotational free energies and application to isotopic fractionation of hydrated chloride ions.

    Science.gov (United States)

    Mielke, Steven L; Truhlar, Donald G

    2009-04-23

    We present two enhancements to our methods for calculating vibrational-rotational free energies by Feynman path integrals, namely, a sequential sectioning scheme for efficiently generating random free-particle paths and a stratified sampling scheme that uses the energy of the path centroids. These improved methods are used with three interaction potentials to calculate equilibrium constants for the fractionation behavior of Cl(-) hydration in the presence of a gas-phase mixture of H(2)O, D(2)O, and HDO. Ion cyclotron resonance experiments indicate that the equilibrium constant, K(eq), for the reaction Cl(H(2)O)(-) + D(2)O right harpoon over left harpoon Cl(D(2)O)(-) + H(2)O is 0.76, whereas the three theoretical predictions are 0.946, 0.979, and 1.20. Similarly, the experimental K(eq) for the Cl(H(2)O)(-) + HDO right harpoon over left harpoon Cl(HDO)(-) + H(2)O reaction is 0.64 as compared to theoretical values of 0.972, 0.998, and 1.10. Although Cl(H(2)O)(-) has a large degree of anharmonicity, K(eq) values calculated with the harmonic oscillator rigid rotator (HORR) approximation agree with the accurate treatment to within better than 2% in all cases. Results of a variety of electronic structure calculations, including coupled cluster and multireference configuration interaction calculations, with either the HORR approximation or with anharmonicity estimated via second-order vibrational perturbation theory, all agree well with the equilibrium constants obtained from the analytical surfaces.

  9. Chloride ingress prediction

    DEFF Research Database (Denmark)

    Frederiksen, Jens Mejer; Geiker, Mette Rica

    2008-01-01

    Prediction of chloride ingress into concrete is an important part of durability design of reinforced concrete structures exposed to chloride containing environment. This paper presents experimentally based design parameters for Portland cement concretes with and without silica fume and fly ash...... in marine atmospheric and submersed South Scandinavian environment. The design parameters are based on sequential measurements of 86 chloride profiles taken over ten years from 13 different types of concrete. The design parameters provide the input for an analytical model for chloride profiles as function...

  10. 离子色谱法测定饮用水中氯化物的不确定度评定%Uncertainty Evaluation of the Determination of Chloride Ion Concentration in Drinking Water by Ion Chromatogram(IC)

    Institute of Scientific and Technical Information of China (English)

    封蓉芳; 陈军; 缪英

    2011-01-01

    目的:为减少实验误差,提高检测结果精确度,评定水中氯化物的不确定度。方法:分析水中氯化物不确定度的来源,通过计算得出该法测定水中氯化物的扩展不确定度。结果:测量结果表明扩展不确定度U95=0.54mg/L,适用于每个水样的检测结果。结论:该方法简便,适合于每一个样本的检测结果,可参考用于水中某些检测参数的不确定评定。%Objective : To evaluate the uncertainty of measuring Cl-concentration in drinking water.This study was to decrease experimental error and increase the accuracy of results.Methods: The source of Measurement uncertainty of the chloride determination in wate

  11. Effects of cyclic chloride exposure on penetration of concrete cover

    Energy Technology Data Exchange (ETDEWEB)

    Hong, K.; Hooton, R.D.

    1999-09-01

    Concretes are in a state of flux between saturated and partially saturated conditions as they undergo continuous cycles of wetting and drying. In saturated concrete, dissolved ions enter through diffusion, whereas in partially saturated concrete, ion-containing fluids are absorbed by capillary suction and concentrated by evaporation of water. The primary focus of this study was to examine the effects of cyclic wetting and drying with sodium chloride solution on chloride ingress into concrete. Chloride profiles of samples exposed to various lengths and numbers of cycles were determined for three mixtures of concrete: two containing slag and/or silica fume with a 0.4 w/cm (water to cementing materials ratio) and one with a 0.3 w/cm. It was found that longer drying times increase the rate of chloride ingress. A good relationship exists between the depth of chloride penetration and the square root of the number of cycles.

  12. 活化煤矸石改性混凝土的抗氯离子渗透性能%Anti⁃chloride Ion Diffusion Property of Concrete Modified by Activated Coal Gangue

    Institute of Scientific and Technical Information of China (English)

    莫金川; 欧忠文; 赵栩欣; 李月霞

    2012-01-01

      采用活化煤矸石作为矿物掺合料配制煤矸石混凝土,研究活化煤矸石对混凝土抗氯离子渗透性能的影响.运用机械-热复合活化方式对煤矸石进行活化,采用强度评价法评价活化煤矸石的活性,确定最佳激活条件;利用经最佳激活条件处理的煤矸石按照不同配比制成煤矸石混凝土,采用快速测定法对该混凝土进行抗氯离子性能测试.研究发现:球磨3 h并经800℃煅烧的煤矸石,抗压强度评价系数达到80.9%;经过该条件处理的煤矸石掺量为30%、水胶比为0.4、砂率为0.35时,氯离子扩散系数最小,为6.3564μm2/s.通过数据拟合得出混凝土氯离子扩散系数同活化煤矸石掺量之间的函数关系,可用以确定一定范围内活化煤矸石掺量对改性混凝土中氯离子扩散系数的影响.%  In order to research the effects of activated coal gangue for the concrete anti-chloride ion diffusion property,concrete is prepared by using activated coal gangue as the mineral mixture. Coal gangue is activated by machinery-thermal activation method at first,and then its activity is evaluated to get the best activity condition by activity evaluation method. The coal gangue which is acti-vated by the best activity condition is used to prepare different mixing ratios’concrete and testing its anti-chloride ion diffusion prop-erty by rapid assessment method (RAM). The strength evaluation coefficient of activated coal gangue after 3 h milling and 800℃burning can get to 80.9%. The Cl-diffusion coefficient of as-prepared concrete can reach the minimum value 6.356 4μm2/s when the mix ratio of activated coal gangue to raw content is 30%,the water/binder ratio 0.4 and the sand ratio 0.35. The function relation of the Cl-diffusion coefficient and the volume of activated coal gangue can be obtained by data fitting,and can be applied for determin-ing the impact of activated-coal-gangue mix ratio on the Cl

  13. Comment on "Local impermeant anions establish the neuronal chloride concentration".

    Science.gov (United States)

    Voipio, Juha; Boron, Walter F; Jones, Stephen W; Hopfer, Ulrich; Payne, John A; Kaila, Kai

    2014-09-05

    Glykys et al. (Reports, 7 February 2014, p. 670) conclude that, rather than ion transporters, "local impermeant anions establish the neuronal chloride concentration" and thereby determine "the magnitude and direction of GABAAR currents at individual synapses." If this were possible, perpetual ion-motion machines could be constructed. The authors' conclusions conflict with basic thermodynamic principles.

  14. Lithium Sulfuryl Chloride Battery.

    Science.gov (United States)

    Primary batteries , Electrochemistry, Ionic current, Electrolytes, Cathodes(Electrolytic cell), Anodes(Electrolytic cell), Thionyl chloride ...Phosphorus compounds, Electrical conductivity, Calibration, Solutions(Mixtures), Electrical resistance, Performance tests, Solvents, Lithium compounds

  15. Chloride binding site of neurotransmitter sodium symporters.

    Science.gov (United States)

    Kantcheva, Adriana K; Quick, Matthias; Shi, Lei; Winther, Anne-Marie Lund; Stolzenberg, Sebastian; Weinstein, Harel; Javitch, Jonathan A; Nissen, Poul

    2013-05-21

    Neurotransmitter:sodium symporters (NSSs) play a critical role in signaling by reuptake of neurotransmitters. Eukaryotic NSSs are chloride-dependent, whereas prokaryotic NSS homologs like LeuT are chloride-independent but contain an acidic residue (Glu290 in LeuT) at a site where eukaryotic NSSs have a serine. The LeuT-E290S mutant displays chloride-dependent activity. We show that, in LeuT-E290S cocrystallized with bromide or chloride, the anion is coordinated by side chain hydroxyls from Tyr47, Ser290, and Thr254 and the side chain amide of Gln250. The bound anion and the nearby sodium ion in the Na1 site organize a connection between their coordinating residues and the extracellular gate of LeuT through a continuous H-bond network. The specific insights from the structures, combined with results from substrate binding studies and molecular dynamics simulations, reveal an anion-dependent occlusion mechanism for NSS and shed light on the functional role of chloride binding.

  16. Chloride equilibrium potential in salamander cones

    Directory of Open Access Journals (Sweden)

    Bryson Eric J

    2004-12-01

    Full Text Available Abstract Background GABAergic inhibition and effects of intracellular chloride ions on calcium channel activity have been proposed to regulate neurotransmission from photoreceptors. To assess the impact of these and other chloride-dependent mechanisms on release from cones, the chloride equilibrium potential (ECl was determined in red-sensitive, large single cones from the tiger salamander retinal slice. Results Whole cell recordings were done using gramicidin perforated patch techniques to maintain endogenous Cl- levels. Membrane potentials were corrected for liquid junction potentials. Cone resting potentials were found to average -46 mV. To measure ECl, we applied long depolarizing steps to activate the calcium-activated chloride current (ICl(Ca and then determined the reversal potential for the current component that was inhibited by the Cl- channel blocker, niflumic acid. With this method, ECl was found to average -46 mV. In a complementary approach, we used a Cl-sensitive dye, MEQ, to measure the Cl- flux produced by depolarization with elevated concentrations of K+. The membrane potentials produced by the various high K+ solutions were measured in separate current clamp experiments. Consistent with electrophysiological experiments, MEQ fluorescence measurements indicated that ECl was below -36 mV. Conclusions The results of this study indicate that ECl is close to the dark resting potential. This will minimize the impact of chloride-dependent presynaptic mechanisms in cone terminals involving GABAa receptors, glutamate transporters and ICl(Ca.

  17. 干湿交替下受弯开裂混凝土梁内氯离子侵蚀试验研究%EXPERIMENTAL STUDY OF THE CHLORIDE ION EROSION IN FLEXURAL CRACKED CONCRETE BEAMS UNDER DRYING-WETTING CYCLES

    Institute of Scientific and Technical Information of China (English)

    崔钊玮; 陆春华; 刘荣桂; 胡白香

    2013-01-01

    分析干湿交替对受弯开裂混凝土梁内氯离子侵蚀的影响,建立考虑表层对流区影响的氯离子等效扩散模型,并借助氯盐干湿循环试验对此模型进行验证。经过30个干湿循环后,采用快速氯离子含量检测( RCT)法,对各裂缝处及其周围混凝土内自由氯离子浓度进行测定。试验结果表明:干湿交替下,完好及受弯开裂混凝土的表层对流区深度在10~15 mm;弯曲裂缝(宽度不大于0.339 mm)截面处,对流区以内混凝土同一深度处自由氯离子浓度比完好处显著提高,且同一裂缝处的浓度分布符合扩散的基本规律;裂缝周围一定范围内混凝土的自由氯离子浓度随距裂缝横向距离的增大而减小,超过一定范围后,弯曲拉应力对混凝土氯离子渗透性能有一定的提高作用;经回归,裂缝处(宽度不大于0.339 mm)等效氯离子扩散系数Deq ( t)与裂缝宽度w之间存在二次函数关系。%The influence of drying-wetting cycles on chloride penetration in flexural cracked concrete was analyzed , and an equivalent chloride diffusion model while considering the effect of surface convection zone was built .The model was verified by the experimental chloride drying-wetting cycles.After 30 cycles, the rapid chloride test (RCT) was used for measuring free chloride ion content of concrete at each cracked section and surrounding sections .Test results showed that under drying-wetting cycles , the depth of convection region in the sound and flexural cracked concrete was about from 10 to 15 mm; at flexural cracked sections , free chloride concentration of the same depth within convection zone increased significantly , and the concentration distribution accorded with the basic diffusion law;a certain range from cracks , free chloride ion content decreased as the horizontal distance from crack extended ;beyond the range , bending tensile stress improved the chloride

  18. Catalytic Conversion of Cellulose to Levulinic Acid by Metal Chlorides

    Directory of Open Access Journals (Sweden)

    Beixiao Zhang

    2010-08-01

    Full Text Available The catalytic performance of various metal chlorides in the conversion of cellulose to levulinic acid in liquid water at high temperatures was investigated. The effects of reaction parameters on the yield of levulinic acid were also explored. The results showed that alkali and alkaline earth metal chlorides were not effective in conversion of cellulose, while transition metal chlorides, especially CrCl3, FeCl3 and CuCl2 and a group IIIA metal chloride (AlCl3, exhibited high catalytic activity. The catalytic performance was correlated with the acidity of the reaction system due to the addition of the metal chlorides, but more dependent on the type of metal chloride. Among those metal chlorides, chromium chloride was found to be exceptionally effective for the conversion of cellulose to levulinic acid, affording an optimum yield of 67 mol % after a reaction time of 180 min, at 200 °C, with a catalyst dosage of 0.02 M and substrate concentration of 50 wt %. Chromium metal, most of which was present in its oxide form in the solid sample and only a small part in solution as Cr3+ ion, can be easily separated from the resulting product mixture and recycled. Finally, a plausible reaction scheme for the chromium chloride catalyzed conversion of cellulose in water was proposed.

  19. Interpretation of postmortem vitreous concentrations of sodium and chloride.

    Science.gov (United States)

    Zilg, B; Alkass, K; Berg, S; Druid, H

    2016-06-01

    Vitreous fluid can be used to analyze sodium and chloride levels in deceased persons, but it remains unclear to what extent such results can be used to diagnose antemortem sodium or chloride imbalances. In this study we present vitreous sodium and chloride levels from more than 3000 cases. We show that vitreous sodium and chloride levels both decrease with approximately 2.2mmol/L per day after death. Since potassium is a well-established marker for postmortem interval (PMI) and easily can be analyzed along with sodium and chloride, we have correlated sodium and chloride levels with the potassium levels and present postmortem reference ranges relative the potassium levels. We found that virtually all cases outside the reference range show signs of antemortem hypo- or hypernatremia. Vitreous sodium or chloride levels can be the only means to diagnose cases of water or salt intoxication, beer potomania or dehydration. We further show that postmortem vitreous sodium and chloride strongly correlate and in practice can be used interchangeably if analysis of one of the ions fails. It has been suggested that vitreous sodium and chloride levels can be used to diagnose drowning or to distinguish saltwater from freshwater drowning. Our results show that in cases of freshwater drowning, vitreous sodium levels are decreased, but that this mainly is an effect of postmortem diffusion between the eye and surrounding water rather than due to the drowning process, since the decrease in sodium levels correlates with immersion time.

  20. Interactions between chloride and cement-paste materials.

    Science.gov (United States)

    Barberon, Fabien; Baroghel-Bouny, Véronique; Zanni, Hélène; Bresson, Bruno; d'Espinose de la Caillerie, Jean-Baptiste; Malosse, Lucie; Gan, Zehong

    2005-02-01

    The durability of cement-based materials with respect to exterior aggressions is one of the current priorities in civil engineering. Depending on their use, the cement-based materials can be exposed to different types of aggressive environments. For instance, damages to concrete structures in contact with a saline environment (sea water on bridges, deicing salts on roads, etc.) are of utmost importance. Upon exposure to saline water, Cl- ions penetrate into the structures and subsequently lead to reinforcement corrosion. Chloride attack is often combined with other aggressive influences such as temperature (e.g., freezing) or the ingress of other ions (e.g., sulfates in sea water). We therefore aim to explore the effect of sodium chloride (NaCl) on the structural chemistry of cement paste. Existing studies about reinforcement corrosion by chloride have focused on the penetration of Cl- ions and the comparison between "free" ions (water-soluble ions) and bound ones. However, little is known about the fixation mechanisms, the localization of Cl in the cement matrix and the structural interaction between Cl and the silicate and aluminate hydrate phases present in cement paste. We present here results of a multinuclear nuclear magnetic resonance study on the fixation of chloride in the hydration products and the characterization of new phases potentially appearing due to chloride ingress.

  1. Durability Analysis of Subway Station in Chloride Environment

    OpenAIRE

    Yang LuFeng; Yu Bo; Hong Bin

    2013-01-01

    In this study, a finite element model for chloride ions transport in saturated concrete was proposed based on the Fick’s second law of diffusion. The governing partial differential equation was solved numerically in space as a boundary-value problem and in time as an initial-value problem by means of the finite element formulations. The maximum allowable value of chloride diffusion coefficient within different locations of subway station with service life of 100a was achieved and suggestions ...

  2. cis-Dichloridobis(1,10-phenanthrolinechromium(III chloride

    Directory of Open Access Journals (Sweden)

    Xiaoli Gao

    2011-02-01

    Full Text Available In the title complex, [CrCl2(C12H8N22]Cl, the CrIII ion is situated on a twofold rotation axis and displays a slightly distorted octahedral CrCl2N4 coordination geometry. The Cr environment is composed of a cis arrangement of two 1,10-phenanthroline and two chloride ligands. The chloride counter-anion exhibits half-occupation and is equally disordered over two positions.

  3. Microwave evaluation of accelerated chloride ingress in mortar

    Science.gov (United States)

    Hu, C.; Case, T.; Castle, M.; Zoughi, R.; Kurtis, K.

    2001-04-01

    Corrosion of steel in reinforced concrete structures can be induced by the presence of chloride ions near the steel/concrete interface. To show the potential of microwave nondestructive testing techniques for evaluating chloride ingress, 8″×8″×8″ mortar specimens with different mixture designs were prepared. To accelerate chloride ingress, they were exposed to cyclical wet/dry conditions, where the wet condition included exposure to salt bath. A complete discussion of the results will be presented in this paper.

  4. The ionic product of water in concentrated tetramethylammonium chloride solutions.

    Science.gov (United States)

    Sipos, P; Bódi, I; May, P M; Hefter, G T

    1997-04-01

    The ionic product of water, pK(w) = - log[H(+)][OH(-)] has been determined in aqueous solutions of tetramethylammonium chloride over the concentration range of 0.1-5.5 M at 25 degrees C using high-precision glass electrode potentiometric titrations. pK(w) data relating to aqueous potassium and sodium chlorides at ionic strengths up to 5 M are markedly lower than the tetramethylammonium chloride results. These differences are almost certainly due to weak associations between potassium and (especially) sodium and hydroxide ions.

  5. Dynamic [Cl-]i measurement with chloride sensing quantum dots nanosensor in epithelial cells

    Science.gov (United States)

    Wang, Yuchi; Mao, Hua; Wong, Lid B.

    2010-02-01

    We have synthesized a chloride sensing quantum dots (QD) nanosensor, Cl-QD, for the dynamic measurements of chloride ion concentration in the millimolar range, a sensitivity that is applicable to most physiological intracellular chloride ion concentration ([Cl-]i) measurements in epithelial cells. The Cl-QD is synthesized by conjugating an anion receptor, 1-(2-mercapto-ethyl)-3-phenyl-thiourea (MEPTU) to a water soluble CdSe/ZnS QD at an emission wavelength of 620 nm. Upon binding of chloride ions to the Cl-QD, a photo-induced electron transfer mechanism caused the fluorescence of the QD to quench. This resulted in an inversely proportional relationship between the chloride ion concentration and the fluorescence intensity of the Cl-QD. We have utilized this Cl-QD to measure [Cl-]i in T84 and CF-PAC cultured cells, with either the C1C-2 or CFTR chloride channels being manipulated by pharmacological chloride channel activators and inhibitors. Activations of C1C-2 and CFTR chloride channels in T84 by the respective lubiprostone and genistein caused predictive increases in the fluorescence of the Cl-QD, i.e., a decrease of [Cl-]i. Conversely, glibenclamide, a chloride channel inhibitor, applied to the CF-PAC cells caused a predictable decrease in the fluorescence of Cl-QD due to the increase of [Cl-]i. These are the first data in using QD-based chloride ion sensors for dynamic measurements of intracellular chloride ion concentrations in epithelial cells.

  6. Dynamic [Cl{sup -}]{sub i} measurement with chloride sensing quantum dots nanosensor in epithelial cells

    Energy Technology Data Exchange (ETDEWEB)

    Wang Yuchi; Mao Hua; Wong, Lid B, E-mail: ywang@biotechplex.com [BioTechPlex Corporation, 1205 Linda Vista Drive Suite A, San Marcos, CA 92078 (United States); Cytoptics Corporation, 1205 Linda Vista Drive Suite B, San Marcos, CA 92078 (United States)

    2010-02-05

    We have synthesized a chloride sensing quantum dots (QD) nanosensor, Cl-QD, for the dynamic measurements of chloride ion concentration in the millimolar range, a sensitivity that is applicable to most physiological intracellular chloride ion concentration ([Cl{sup -}]{sub i}) measurements in epithelial cells. The Cl-QD is synthesized by conjugating an anion receptor, 1-(2-mercapto-ethyl)-3-phenyl-thiourea (MEPTU) to a water soluble CdSe/ZnS QD at an emission wavelength of 620 nm. Upon binding of chloride ions to the Cl-QD, a photo-induced electron transfer mechanism caused the fluorescence of the QD to quench. This resulted in an inversely proportional relationship between the chloride ion concentration and the fluorescence intensity of the Cl-QD. We have utilized this Cl-QD to measure [Cl{sup -}]{sub i} in T84 and CF-PAC cultured cells, with either the C1C-2 or CFTR chloride channels being manipulated by pharmacological chloride channel activators and inhibitors. Activations of C1C-2 and CFTR chloride channels in T84 by the respective lubiprostone and genistein caused predictive increases in the fluorescence of the Cl-QD, i.e., a decrease of [Cl{sup -}]{sub i}. Conversely, glibenclamide, a chloride channel inhibitor, applied to the CF-PAC cells caused a predictable decrease in the fluorescence of Cl-QD due to the increase of [Cl{sup -}]{sub i}. These are the first data in using QD-based chloride ion sensors for dynamic measurements of intracellular chloride ion concentrations in epithelial cells.

  7. Raman and DFT Study on N-H+…Cl- Hydrogen Bonding in 1,1,3,3-Tetra-Methylguanidinium Chloride forming an Ion-pair Molecule in the Vapor Phase

    DEFF Research Database (Denmark)

    Berg, Rolf W.; Riisager, Anders; Fehrmann, Rasmus

    The chemistry of 1,1,3,3-tetramethylguanidinium ([TMGH]+) chloride, a low temperature (molten) ionic liquid, is discussed, based on its Raman spectra associated with ab initio molecular orbital DFT-type quantum mechanical calculations (with 6-311+G(d,p) basis sets) on “molecules” in isolated gase...

  8. An experiment on multibubble sonoluminescence spectra in sodium chloride solution

    Institute of Scientific and Technical Information of China (English)

    CHEN Zhan; XU JunFeng; HUANG Wei; CHEN WeiZhong; MIAO GuoQing

    2008-01-01

    We investigated experimentally the spectra of MBSL in sodium chloride water solution with krypton as dissolved gas. We observed and compared the spectra of hydroxyl ion at 310 nm and that of sodium atom at 589 nm. It has been found that under the same experimental condition, the intensity of sodium atom spectra is obviously higher than that of the hydroxyl ion spectra, and is more sensitive to the experimental condition. The krypton content, the concentration of sodium chloride solution, and the driving sound pressure obviously affect the spectra intensity in certain range.

  9. Extractive process for preparing high purity magnesium chloride hexahydrate

    Directory of Open Access Journals (Sweden)

    Fezei Radouanne

    2012-01-01

    Full Text Available This paper refers a method for the preparation of magnesium chloride hexahydrate (bischofite from Sebkha el Melah of Zarzis Tunisian natural brine. It is a five-stage process essentially based on crystallization by isothermal evaporation and chemical precipitation. The two first steps were dedicated to the crystallization of sodium chloride and potassiummagnesium double salts, respectively. Then, the resulting liquor was desulfated using calcium chloride solution. After that another isothermal evaporation stage was implemented in order to eliminate potassium ions in the form of carnallite, KCl.MgCl2.6H2O. At the end of this step, the recovered solution primarily composed of magnesium and chloride ions was treated by dioxan in order to precipitate magnesium chloride as MgCl2.6H2O.C4H8O2. This compound dried at constant temperature of 100°C gave good quality magnesium chloride hexahydrate. Besides this salt, the various by-products obtained from the different treatment stages are also useful.

  10. Enhanced expression of potassium-chloride cotransporter KCC2 in human temporal lobe epilepsy

    OpenAIRE

    Karlócai, MR; Wittner, L; Tóth, K; Maglóczky, Z.; Katarova, Z.; Rásonyi, G; Erőss, L; Czirják, S; Halász, P; G. Szabó; Payne, JA; Kaila, K.; Freund, TF

    2015-01-01

    © 2015 Springer-Verlag Berlin Heidelberg Synaptic reorganization in the epileptic hippocampus involves altered excitatory and inhibitory transmission besides the rearrangement of dendritic spines, resulting in altered excitability, ion homeostasis, and cell swelling. The potassium-chloride cotransporter-2 (KCC2) is the main chloride extruder in neurons and hence will play a prominent role in determining the polarity of GABAA receptor-mediated chloride currents. In addition, KCC2 also interact...

  11. Hydrolysis of ferric chloride in solution

    Energy Technology Data Exchange (ETDEWEB)

    Lussiez, G.; Beckstead, L.

    1996-11-01

    The Detox{trademark} process uses concentrated ferric chloride and small amounts of catalysts to oxidize organic compounds. It is under consideration for oxidizing transuranic organic wastes. Although the solution is reused extensively, at some point it will reach the acceptable limit of radioactivity or maximum solubility of the radioisotopes. This solution could be cemented, but the volume would be increased substantially because of the poor compatibility of chlorides and cement. A process has been developed that recovers the chloride ions as HCl and either minimizes the volume of radioactive waste or permits recycling of the radioactive chlorides. The process involves a two-step hydrolysis at atmospheric pressure, or preferably under a slight vacuum, and relatively low temperature, about 200{degrees}C. During the first step of the process, hydrolysis occurs according to the reaction below: FeCl{sub 3 liquid} + H{sub 2}O {r_arrow} FeOCl{sub solid} + 2 HCl{sub gas} During the second step, the hot, solid, iron oxychloride is sprayed with water or placed in contact with steam, and hydrolysis proceeds to the iron oxide according to the following reaction: 2 FeOCl{sub solid} + H{sub 2}O {r_arrow} Fe{sub 2}O{sub 3 solid} + 2 HCl{sub gas}. The iron oxide, which contains radioisotopes, can then be disposed of by cementation or encapsulation. Alternately, these chlorides can be washed off of the solids and can then either be recycled or disposed of in some other way.

  12. Benzalkonium Chloride and Glaucoma

    OpenAIRE

    Rasmussen, Carol A.; Kaufman, Paul L.; Kiland, Julie A.

    2014-01-01

    Glaucoma patients routinely take multiple medications, with multiple daily doses, for years or even decades. Benzalkonium chloride (BAK) is the most common preservative in glaucoma medications. BAK has been detected in the trabecular meshwork (TM), corneal endothelium, lens, and retina after topical drop installation and may accumulate in those tissues. There is evidence that BAK causes corneal and conjunctival toxicity, including cell loss, disruption of tight junctions, apoptosis and preapo...

  13. Analysis of chloride diffusivity in concrete containing red mud

    Directory of Open Access Journals (Sweden)

    D.V. Ribeiro

    Full Text Available Red mud is a solid waste produced in the alumina production process and, due to its high pH, is classified as hazardous. Its incorporation in concrete mixtures, acting as filler due to the particles fineness, might be an interesting reuse alternative. The focus of this paper is to study the chloride diffusivity of concrete mixtures containing red-mud. The concentration of chlorides was monitored by measuring the conductivity of the anolyte, which was distilled water initially. In addition, the estimation of the chloride ions diffusion coefficients in steady and non-steady conditions, Ds and Dns, was obtained from the ''time-lag'' and ''equivalent time'' between diffusion and migration experiments. Due to superfine particle-size distribution and the "filler" effect, the red mud addition seems to assure lower chloride diffusivity.

  14. Prediction of chloride ingress and binding in cement paste

    DEFF Research Database (Denmark)

    Geiker, Mette Rica; Nielsen, Erik Pram; Herforth, Duncan

    2007-01-01

    This paper summarizes recent work on an analytical model for predicting the ingress rate of chlorides in cement-based materials. An integral part of this is a thermodynamic model for predicting the phase equilibria in hydrated Portland cement. The model’s ability to predict chloride binding...... in Portland cement pastes at any content of chloride, alkalis, sulfates and carbonate was verified experimentally and found to be equally valid when applied to other data in the literature. The thermodynamic model for predicting the phase equilibria in hydrated Portland cement was introduced into an existing...... Finite Difference Model for the ingress of chlorides into concrete which takes into account its multi-component nature. The “composite theory” was then used to predict the diffusivity of each ion based on the phase assemblage present in the hydrated Portland cement paste. Agreement was found between...

  15. 离子色谱法测定奶粉中氯化胆碱、钠、钾、镁、钙的含量%Determination of Choline Chloride,Na^+,K^+, Mg^2+ and Ca^2+ in Milk Powder by Ion Chromatography

    Institute of Scientific and Technical Information of China (English)

    曹文军; 崔晗; 沈葆真; 苏海滨; 贺舒文; 黄大亮; 李莉

    2012-01-01

    A method was established to determine choline chloride,Na+,K+,Mg2+ and Ca2+ in milk powder by using ion exchange chromatography with conductivity detector.The samples were separated on a IonPac CS-12A(250mm×4 mm) cation exchange column using gradient elution of MSA,and the velocity was 1.0 mL/min.The detection limit of the method was 0.5~10 mg/L.The relative standard deviation of this method is 2.3%-4.7%(n=6)and the recovery is the range of 74.7%~93.5%.The method is accurate and simple,and is suitable for rapid detection choline chloride,Na+,K+,Mg2+ and Ca2+in milk powder.%建立离子色谱定量测定奶粉中钠、钾、氯化胆碱、镁、钙的方法,应用IonPac CS-12A(250 mm×4 mm)阳离子交换柱,淋洗液为20 mmol/L MSA,等浓度淋洗,流速为1.0 mL/min,电导检测器检测,方法检出限为0.5~10 mg/kg。6次测定平行样,相对标准偏差2.3%~4.7%,5种阳离子加标回收率74.7%~93.5%,该方法具有准确、操作简便等特点,可用于奶粉中钠、钾、氯化胆碱、镁、钙的检测。

  16. Electrochemical activity of heavy metal oxides in the process of chloride induced corrosion of steel reinforcement

    Indian Academy of Sciences (India)

    V Živica

    2002-10-01

    The influence of heavy metal oxides on the chloride induced corrosion of steel reinforcement in concrete was studied. Significant inhibition and stimulation of chloride induced corrosion have been observed. Basicity and acidity of the relevant metal ions, and their ability to form complexes are considered as the main factors of the observed effects.

  17. Mechanism of chloride interaction with neurotransmitter:sodium symporters.

    Science.gov (United States)

    Zomot, Elia; Bendahan, Annie; Quick, Matthias; Zhao, Yongfang; Javitch, Jonathan A; Kanner, Baruch I

    2007-10-11

    Neurotransmitter:sodium symporters (NSS) have a critical role in regulating neurotransmission and are targets for psychostimulants, anti-depressants and other drugs. Whereas the non-homologous glutamate transporters mediate chloride conductance, in the eukaryotic NSS chloride is transported together with the neurotransmitter. In contrast, transport by the bacterial NSS family members LeuT, Tyt1 and TnaT is chloride independent. The crystal structure of LeuT reveals an occluded binding pocket containing leucine and two sodium ions, and is highly relevant for the neurotransmitter transporters. However, the precise role of chloride in neurotransmitter transport and the location of its binding site remain elusive. Here we show that introduction of a negatively charged amino acid at or near one of the two putative sodium-binding sites of the GABA (gamma-aminobutyric acid) transporter GAT-1 from rat brain (also called SLC6A1) renders both net flux and exchange of GABA largely chloride independent. In contrast to wild-type GAT-1, a marked stimulation of the rate of net flux, but not of exchange, was observed when the internal pH was lowered. Equivalent mutations introduced in the mouse GABA transporter GAT4 (SLC6A11) and the human dopamine transporter DAT (SLC6A3) also result in chloride-independent transport, whereas the reciprocal mutations in LeuT and Tyt1 render substrate binding and/or uptake by these bacterial NSS chloride dependent. Our data indicate that the negative charge, provided either by chloride or by the transporter itself, is required during binding and translocation of the neurotransmitter, probably to counterbalance the charge of the co-transported sodium ions.

  18. The Use of Electrodiffusion for Removing Chlorides from Concrete

    OpenAIRE

    2016-01-01

    The article presents a description of ion migration in a concrete pore liquid caused by an external electric field. The equation of the flow of aggressive chloride ions is formulated on the basis of partial equations of mass balance. It is assumed that electrochemical potential is in classical form, then an attempt is made to determine the average diffusion coefficient using the inverse diffusion Eq.(3.9).

  19. The Use of Electrodiffusion for Removing Chlorides from Concrete

    Science.gov (United States)

    Alsabry, A.

    2016-12-01

    The article presents a description of ion migration in a concrete pore liquid caused by an external electric field. The equation of the flow of aggressive chloride ions is formulated on the basis of partial equations of mass balance. It is assumed that electrochemical potential is in classical form, then an attempt is made to determine the average diffusion coefficient using the inverse diffusion Eq.(3.9).

  20. Oxomemazine hydro-chloride.

    Science.gov (United States)

    Siddegowda, M S; Butcher, Ray J; Akkurt, Mehmet; Yathirajan, H S; Ramesh, A R

    2011-08-01

    IN THE TITLE COMPOUND [SYSTEMATIC NAME: 3-(5,5-dioxo-phen-othia-zin-10-yl)-N,N,2-trimethyl-propanaminium chloride], C(18)H(23)N(2)O(2)S(+)·Cl(-), the dihedral angle between the two outer aromatic rings of the phenothia-zine unit is 30.5 (2)°. In the crystal, the components are linked by N-H⋯Cl and C-H⋯Cl hydrogen bonds and C-H⋯π inter-actions.

  1. Separating refractory and non-refractory particulate chloride and estimating chloride depletion by aerosol mass spectrometry in a marine environment

    Directory of Open Access Journals (Sweden)

    I. Nuaaman

    2015-01-01

    Full Text Available Aerosol composition and concentration measurements along the coast of California were obtained using an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-AMS onboard the research vessel Atlantis during the CalNex study in 2010. This paper focuses on the measurement of aerosol chloride using the HR-AMS that can be ambiguous in regions with significant quantities of sea salt aerosols. This ambiguity arises due to large differences in the sensitivity of the HR-AMS to refractory chloride species (i.e., NaCl and non refractory chloride species (i.e., NH4Cl, HCl, etc.. Using the HR-AMS, the aerosol chloride signal is typically quantified using ion signals for 35Cl+, H35Cl+, 37Cl+ and H37Cl+ (HxCl+. During this study, the highest aerosol chloride signal was observed during sea sweep experiments when the source of the aerosol chloride was NaCl present in artificially generated sea salt aerosols even though the HR-AMS has significantly lower sensitivity to such refractory species. Other prominent ion signals that arise from NaCl salt were also observed at m/z 22.99 for Na+ and m/z 57.96 for Na35Cl+ during both sea sweep experiments and during periods of ambient measurements. Thus, refractory NaCl contributes significantly to the HxCl+ signal, interfering with attempts to quantify non sea salt chloride (nssCl. It was found that during ambient aerosol measurements, the interference in the HxCl+ signal from sea salt chloride (ssCl was as high as 89%, but with a study wide average of 10%. The Na35Cl+ ion signal was found to be a good tracer for NaCl. We outline a method to establish nssCl in the ambient aerosols by subtracting the sea salt chloride (ssCl signal from the HxCl+ signal. The ssCl signal is derived from the Na35Cl+ ion tracer signal and the HxCl+ to Na35Cl+ ratio established from the sea sweep experiments. Ambient submicron concentrations of ssCl were also established using the

  2. Boldine action against the stannous chloride effect.

    Science.gov (United States)

    Reiniger, I W; Ribeiro da Silva, C; Felzenszwalb, I; de Mattos, J C; de Oliveira, J F; da Silva Dantas, F J; Bezerra, R J; Caldeira-de-Araújo, A; Bernardo-Filho, M

    1999-12-15

    Peumus boldus extract has been used in popular medicine in the treatment of biliar litiase, hepatic insufficiency and liver congestion. Its effects are associated to the substance boldine that is present in its extract. In the present work, we evaluated the influence of boldine both in: (i) the structural conformation of a plasmid pUC 9.1 through gel electrophoresis analysis; and in (ii) the survival of the strain of Escherichia coli AB1157 submitted to reactive oxygen species (ROS), generated by a Fenton like reaction, induced by stannous chloride. Our results show a reduction of the lethal effect induced by stannous chloride on the survival of the E. coli culture in the presence of boldine. The supercoiled form of the plasmid is not modified by stannous chloride in the presence of boldine. We suggest that the protection induced by boldine could be explained by its anti-oxidant mechanism. In this way, the boldine could be reacting with stannous ions, protecting them against the oxidation and, consequently, avoiding the generation of ROS.

  3. Chloride test - blood

    Science.gov (United States)

    ... disease Antidiuretic hormone blood test Gastric suction Heart failure - overview Hyperventilation Ions Metabolic acidosis Multiple endocrine neoplasia (MEN) II Proximal renal tubular acidosis Respiratory acidosis Sodium blood test Review Date 5/3/2015 Updated by: Laura J. ...

  4. Development and critical evaluation of fluorescent chloride nanosensors.

    Science.gov (United States)

    Graefe, Anja; Stanca, Sarmiza E; Nietzsche, Sandor; Kubicova, Lenka; Beckert, Rainer; Biskup, Christoph; Mohr, Gerhard J

    2008-09-01

    In this study, we describe the preparation and evaluation of new fluorescent sensor nanoparticles for the ratiometric measurement of chloride concentrations. Both a chloride-sensitive dye (lucigenin) and a reference dye (sulforhodamine derivative) were incorporated into polyacrylamide nanoparticles via inverse microemulsion polymerization and investigated for their response to chloride ions in buffered suspension as well as in living cells. The fluorescence intensity of lucigenin reversibly decreased in the presence of chloride ions due to a collisional quenching process, which can be described with the Stern-Volmer equation. The determined Stern-Volmer constant K SV for the quenching of lucigenin incorporated into particles was found to be 53 M (-1) and is considerably smaller than the Stern-Volmer constant for quenching of free lucigenin ( K SV = 250 M (-1)) under the same conditions. To test the nanosensors in living cells, we incorporated them into Chinese hamster ovary cells and mouse fibroblasts by using the conventional lipofectamin technique and monitored the response to changing chloride concentrations in the cell.

  5. A molecular dynamics study of chloride binding by the cryptand SC24

    Science.gov (United States)

    Owenson, B.; MacElroy, R. D.; Pohorille, A.

    1988-01-01

    The capture of chloride from water by the tetraprotonated form of the spherical macrotricyclic molecule SC24 was studied using molecular dynamics simulation methods. This model ionophore represents a broad class of molecules which remove ions from water. Two binding sites for the chloride were found, one inside and one outside the ligand. These sites are separated by a potential energy barrier of approximately 20 kcal mol-1. The major contribution to this barrier comes from dehydration of the chloride. The large, unfavorable dehydration effect is compensated for by an increase in electrostatic attraction between the oppositely charged chloride and cryptand, and by energetically favorable rearrangements of water structure. Additional assistance in crossing the barrier and completing the dehydration of the ion is provided by the shift of three positively charged hydrogen atoms of the cryptand towards the chloride. This structural rigidity is partially responsible for its selectivity.

  6. Multi-scale modelling of uranyl chloride solutions

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Thanh-Nghi; Duvail, Magali, E-mail: magali.duvail@icsm.fr; Villard, Arnaud; Dufrêche, Jean-François, E-mail: jean-francois.dufreche@univ-montp2.fr [Institut de Chimie Séparative de Marcoule (ICSM), UMR 5257, CEA-CNRS-Université Montpellier 2-ENSCM, Site de Marcoule, Bâtiment 426, BP 17171, F-30207 Bagnols-sur-Cèze Cedex (France); Molina, John Jairo [Fukui Institute for Fundamental Chemistry, Kyoto University, Takano-Nishihiraki-cho 34-4, Sakyo-ku, Kyoto 606-8103 (Japan); Guilbaud, Philippe [CEA/DEN/DRCP/SMCS/LILA, Marcoule, F-30207 Bagnols-sur-Cèze Cedex (France)

    2015-01-14

    Classical molecular dynamics simulations with explicit polarization have been successfully used to determine the structural and thermodynamic properties of binary aqueous solutions of uranyl chloride (UO{sub 2}Cl{sub 2}). Concentrated aqueous solutions of uranyl chloride have been studied to determine the hydration properties and the ion-ion interactions. The bond distances and the coordination number of the hydrated uranyl are in good agreement with available experimental data. Two stable positions of chloride in the second hydration shell of uranyl have been identified. The UO{sub 2}{sup 2+}-Cl{sup −} association constants have also been calculated using a multi-scale approach. First, the ion-ion potential averaged over the solvent configurations at infinite dilution (McMillan-Mayer potential) was calculated to establish the dissociation/association processes of UO{sub 2}{sup 2+}-Cl{sup −} ion pairs in aqueous solution. Then, the association constant was calculated from this potential. The value we obtained for the association constant is in good agreement with the experimental result (K{sub UO{sub 2Cl{sup +}}} = 1.48 l mol{sup −1}), but the resulting activity coefficient appears to be too low at molar concentration.

  7. Photonic crystal fiber based chloride chemical sensors for corrosion monitoring

    Science.gov (United States)

    Wei, Heming; Tao, Chuanyi; Krishnaswamy, Sridhar

    2016-04-01

    Corrosion of steel is one of the most important durability issues in reinforced concrete (RC) structures because aggressive ions such as chloride ions permeate concrete and corrode steel, consequently accelerating the destruction of structures, especially in marine environments. There are many practical methods for corrosion monitoring in RC structures, mostly focusing on electrochemical-based sensors for monitoring the chloride ion which is thought as one of the most important factors resulting in steel corrosion. In this work, we report a fiber-optic chloride chemical sensor based on long period gratings inscribed in a photonic crystal fiber (PCF) with a chloride sensitive thin film. Numerical simulation is performed to determine the characteristics and resonance spectral response versus the refractive indices of the analyte solution flowing through into the holes in the PCF. The effective refractive index of the cladding mode of the LPGs changes with variations of the analyte solution concentration, resulting in a shift of the resonance wavelength, hence providing the sensor signal. This fiber-optic chemical sensor has a fast response, is easy to prepare and is not susceptible to electromagnetic environment, and can therefore be of use for structural health monitoring of RC structures subjected to such aggressive environments.

  8. Benzalkonium chloride and glaucoma.

    Science.gov (United States)

    Rasmussen, Carol A; Kaufman, Paul L; Kiland, Julie A

    2014-01-01

    Glaucoma patients routinely take multiple medications, with multiple daily doses, for years or even decades. Benzalkonium chloride (BAK) is the most common preservative in glaucoma medications. BAK has been detected in the trabecular meshwork (TM), corneal endothelium, lens, and retina after topical drop installation and may accumulate in those tissues. There is evidence that BAK causes corneal and conjunctival toxicity, including cell loss, disruption of tight junctions, apoptosis and preapoptosis, cytoskeleton changes, and immunoinflammatory reactions. These same effects have been reported in cultured human TM cells exposed to concentrations of BAK found in common glaucoma drugs and in the TM of primary open-angle glaucoma donor eyes. It is possible that a relationship exists between chronic exposure to BAK and glaucoma. The hypothesis that BAK causes/worsens glaucoma is being tested experimentally in an animal model that closely reflects human physiology.

  9. Chloride on the Move

    KAUST Repository

    Li, Bo

    2017-01-09

    Chloride (Cl−) is an essential plant nutrient but under saline conditions it can accumulate to toxic levels in leaves; limiting this accumulation improves the salt tolerance of some crops. The rate-limiting step for this process – the transfer of Cl− from root symplast to xylem apoplast, which can antagonize delivery of the macronutrient nitrate (NO3−) to shoots – is regulated by abscisic acid (ABA) and is multigenic. Until recently the molecular mechanisms underpinning this salt-tolerance trait were poorly defined. We discuss here how recent advances highlight the role of newly identified transport proteins, some that directly transfer Cl− into the xylem, and others that act on endomembranes in ‘gatekeeper’ cell types in the root stele to control root-to-shoot delivery of Cl−.

  10. Binding Capacity and Mechanism of Chloride Ion in Activated Coal Gangue Dosage and Cement System%活化煤矸石-水泥凝胶体系对氯离子的结合能力和结合机理

    Institute of Scientific and Technical Information of China (English)

    刘杰

    2012-01-01

    采用化学滴定法系统研究了水胶比为0.4煤矸石掺量分别为0%、20%、30%和40%的水泥-煤矸石凝胶体系对氯离子结合能力的影响规律.通过XRD、DSC和TG-DTG方法,研究其结合机理.结果表明:随煤矸石掺量的增大,结合能力呈现先增加后降低趋势,最佳掺量为30%o超过此值,经DSC和XRD微观分析表明,Friedel盐(简称F盐)含量因水泥浆体的初级水化产物CH含量不足,影响了煤矸石的二次水化反应的发挥而下降.活化煤矸石对氯离子的结合能力一方面因其高铝酸盐含量稀释了硫酸盐,增加AFm相生成,另一方面因其比表面积较大,结构疏松对氯离子有一定吸附作用,同时火山灰效应的发挥生成较多的C-S-H凝胶和水化铝酸盐相,进而促进F盐的形成.%The binding capacity and mechanisms of chloride ion in hydrated cementitious paste ( w/b = 0. 4) with 0% ,20% , 30% and 40% mass fraction of activated coal gangue is respectively investigated by chemical titration analysis, X-Ray Diffractometry ( XRD) , Differential Scanning Calorimetry ( DSC ) and Thermo-gravimetry-Differential Thermogravimetry (TG-DTG). Results indicate that chloride binding capacity of cement-based materials is increased initially and then decreased with increasing of activated coal gangue dosage. Friedel' salt content is dropped due to lack of portlandite in the number of initial hydrated products of cement paste so that influenced second hydration reaction of coal gangue . The reason of activated coal gangue bound chloride ion is as follows. Firstly, coal gangue with higher aluminates content dilutes sulphates and then adds the formation of AFm phase. Secondly, part of chloride ion is absorbed for its higher specific surface area and loose structure. C-S-H gel and hydrated aluminates phase content is enhanced with the pozzolanic effect of activated coal gangue,which is the last, and also the most important for the formation of Friedel' s salt.

  11. Spectrophotometric determination of silica in water. Low range; Determinacion espectrofotometrica de silicio en aguas. Rango bajo

    Energy Technology Data Exchange (ETDEWEB)

    Acosta L, E. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)]. e-mail: eal@nuclear.inin.mx

    1992-07-15

    The spectrophotometric method for the determination of the silica element in water, demineralized water, raw waters, laundry waters, waters treated with ion exchange resins and sea waters is described. This method covers the determination of the silica element in the interval from 20 to 1000 {mu}g/l on 50 ml. of base sample. These limits its can be variable if the size of the used aliquot one is changed for the final determination of the silica element. (Author)

  12. INVESTIGATION OF CHLORIDE ION PERMEABILITY BY PERMIT METHOD AND ITS CORRELATION WITH POROSITY OF CONCRETE%Permit法研究氯离子渗透性及其与混凝土孔隙率的关系

    Institute of Scientific and Technical Information of China (English)

    明静; 张亚梅; 孙伟

    2010-01-01

    应用渗透法(permeation migration,Permit)及快速氯离子迁移法(rapid chloride migration,RCM)研究了水胶比及粉煤灰掺量对混凝土抗氯离子渗透性的影响.通过对比试验,分析了Permit方法与RCM方法试验结果之间的相关性.采用可蒸发水含量法测试了混凝土相应的孔隙率,分析了Permit试验结果与混凝土孔隙率的关系.结果表明:Permit试验测定的混凝上氯离子渗透性指标与RCM试验结果及粗毛细孔孔隙率均具有良好的对应关系.由于是无损检测方法,用于现场测试Permit方法比RCM法更具优越性.

  13. Effects of chloride ion concentration and pH values on the corrosion behavior of Cr12Ni3Co12Mo4W ultra-high-strength martensitic stainless steel

    Science.gov (United States)

    Li, Hui-yan; Dong, Chao-fang; Xiao, Kui; Li, Xiao-gang; Zhong, Ping

    2016-11-01

    The effects of Cl- ion concentration and pH values on the corrosion behavior of Cr12Ni3Co12Mo4W ultra-high-strength martensitic stainless steel (UHSMSS) were investigated by a series of electrochemical tests combined with observations by stereology microscopy and scanning electron microscopy. A critical Cl- ion concentration was found to exist (approximately 0.1wt%), above which pitting occurred. The pitting potential decreased with increasing Cl- ion concentration. A UHSMSS specimen tempered at 600°C exhibited a better pitting corrosion resistance than the one tempered at 400°C. The corrosion current density and passive current density of the UHSMSS tempered at 600°C decreased with increasing pH values of the corrosion solution. The pits developed a shallower dish geometry with increasing polarization potential. A lacy cover on the pits of the UHSMSS tempered at 400°C accelerated pitting, whereas corrosion products deposited in the pits of the UHSMSS tempered at 600°C hindered pitting.

  14. Effects of chloride ion concentration and pH values on the corrosion behavior of Cr12Ni3Co12Mo4W ultra-high-strength martensitic stainless steel

    Institute of Scientific and Technical Information of China (English)

    Hui-yan Li; Chao-fang Dong; Kui Xiao; Xiao-gang Li; Ping Zhong

    2016-01-01

    The effects of Cl− ion concentration and pH values on the corrosion behavior of Cr12Ni3Co12Mo4W ultra-high-strength marten-sitic stainless steel (UHSMSS) were investigated by a series of electrochemical tests combined with observations by stereology microscopy and scanning electron microscopy. A critical Cl− ion concentration was found to exist (approximately 0.1wt%), above which pitting occurred. The pitting potential decreased with increasing Cl− ion concentration. A UHSMSS specimen tempered at 600°C exhibited a better pitting cor-rosion resistance than the one tempered at 400°C. The corrosion current density and passive current density of the UHSMSS tempered at 600°C decreased with increasing pH values of the corrosion solution. The pits developed a shallower dish geometry with increasing polariza-tion potential. A lacy cover on the pits of the UHSMSS tempered at 400°C accelerated pitting, whereas corrosion products deposited in the pits of the UHSMSS tempered at 600°C hindered pitting.

  15. Intervention of phenonium ion in Ritter reactions.

    Science.gov (United States)

    Ho, Tse-Lok; Chein, Rong-Jie

    2004-01-23

    The transformation of phenylethyl chloride to 3,4-dihydroisoquinolines is shown to proceed via phenonium ion. The evidence comes from a study of dideuterated analogue 4, and the monomethylated and dimethylated compounds 2 and 3.

  16. Synthesis, spectroscopic and thermal studies of the copper(II) aspartame chloride complex

    Science.gov (United States)

    Çakır, S.; Coşkun, E.; Naumov, P.; Biçer, E.; Bulut, İ.; İçbudak, H.; Çakır, O.

    2002-08-01

    Aspartame adduct of copper(II) chloride Cu(Asp) 2Cl 2·2H 2O (Asp=aspartame) is synthesized and characterized by elemental analysis, FT IR, UV/vis, ESR spectroscopies, TG, DTG, DTA measurements and molecular mechanics calculations. Aqueous solution of the green solid absorbs strongly at 774 and 367 nm. According to the FT IR spectra, the aspartame moiety coordinates to the copper(II) ion via its carboxylate ends, whereas the ammonium terminal groups give rise to hydrogen bonding network with the water, the chloride ions or neighboring carboxylate groups. The results suggest tetragonally distorted octahedral environment of the copper ions.

  17. Optical, thermal and magnetic studies of pure and cobalt chloride doped L-alanine cadmium chloride

    Science.gov (United States)

    Benila, B. S.; Bright, K. C.; Delphine, S. Mary; Shabu, R.

    2017-03-01

    Single crystals of L-alanine cadmium chloride (LACC) and cobalt chloride (Co2+) doped LACC have been grown by the slow evaporation solution growth technique. The grown crystals were subjected to various characterizations such as powder XRD, SXRD, FTIR, UV-vis, EDAX, TG/DTA, VSM, Dielectric and Second Harmonic Generation (SHG) measurements. The lattice parameters of the grown crystals were determined by single crystal X-ray analysis. EDAX analysis confirms the presence of Co2+ ion in the host material. The functional group and optical behavior of the crystals were identified from FTIR and UV-vis spectrum analysis. Electrical parameters such as dielectric constant, dielectric loss have been studied. The thermal stability of the compound was found out using TGA/DTA analysis. Second Harmonic Generation of the samples was confirmed by Kurtz-Perry powder technique. Magnetic properties of the crystals studied by VSM were also reported. The encouraging results show that the cobalt chloride doped LACC crystals have greater potential applications in optical devices.

  18. Studies Update Vinyl Chloride Hazards.

    Science.gov (United States)

    Rawls, Rebecca

    1980-01-01

    Extensive study affirms that vinyl chloride is a potent animal carcinogen. Epidemiological studies show elevated rates of human cancers in association with extended contact with the compound. (Author/RE)

  19. The Chloride Permeability of Persulphated Phosphogypsum-Slag Cement Concrete

    Institute of Scientific and Technical Information of China (English)

    HUANG Youqiang; LU Jianxin; CHEN Feixiang; SHUI Zhonghe

    2016-01-01

    The chloride permeability and microstructure of persulphated phosphogypsum-slag cement concrete (PPSCC), the Portland slag cement concrete (PSCC) and ordinary Portland cement concrete (OPCC) were investigated comparatively. Some test methods were used to evaluate the chloride permeability and explain the relationship between the permeability and microstructure of concrete. The results show that the resistance to chloride penetration in PPSCC is signiifcantly better than that in OPCC, the reasons are as follows: 1) the slag in PPSCC is activated by clinker (alkali activation) and phosphogypsum (sulfate activation), forming more low Ca/Si C-S-H gel and gel pores below 10 nm than OPCC, improving the resistance to chloride penetration; 2) the hydration products of PPSCC have a much stronger binding capacity for chloride ions; and 3) in the same mix proportion, PPSCC has a better workability without large crystals calcium hydroxide in the hydration products, the interfacial transition zone (ITZ) is smoother and denser, which can cut off the communicating pores between the pastes and aggregates.

  20. Effect of chloride impurities on the performance and durability of polybenzimidazole-based high temperature proton exchange membrane fuel cells

    DEFF Research Database (Denmark)

    Ali, Syed Talat; Li, Qingfeng; Pan, Chao;

    2011-01-01

    The effect of chloride as an air impurity and as a catalyst contaminant on the performance and durability of polybenzimidazole (PBI)-based high temperature proton exchange membrane fuel cell (HT-PEMFC) was studied. The ion chromatographic analysis reveals the existence of chloride contaminations...

  1. Parameters Affecting Hydrogen Chloride Measurements

    Science.gov (United States)

    1993-06-01

    contain sea salt, which is hygroscopic because of the magnesium chloride present, or ammonium bisulfate , which mostly comes from sulfur pollution and is...boosters release hydrogen chloride as a combustion product, and hydrazines or nitric acid can be spilled from liquid fuel motors. Monitoring the...solubility constant, and the second is the acid ionization constant. From experimental work, the product of the two constants is well established (Reference

  2. Influence of chloride on the chronic toxicity of sodium nitrate to Ceriodaphnia dubia and Hyalella azteca.

    Science.gov (United States)

    Soucek, David J; Dickinson, Amy

    2016-09-01

    While it has been well established that increasing chloride concentration in water reduces the toxicity of nitrite to freshwater species, little work has been done to investigate the effect of chloride on nitrate toxicity. We conducted acute and chronic nitrate (as sodium nitrate) toxicity tests with the cladoceran Ceriodaphnia dubia and the amphipod Hyalella azteca (chronic tests only) over a range of chloride concentrations spanning natural chloride levels found in surface waters representative of watersheds of the Great Lakes Region. Chronic nitrate toxicity test results with both crustaceans were variable, with H. azteca appearing to be one of the more sensitive invertebrate species tested and C. dubia being less sensitive. While the variability in results for H. azteca were to an extent related to chloride concentration in test water that was distinctly not the case for C. dubia. We concluded that the chloride dependent toxicity of nitrate is not universal among freshwater crustaceans. An additional sodium chloride chronic toxicity test with the US Lab strain of H. azteca in the present study suggested that when present as predominantly sodium chloride and with relatively low concentrations of other ions, there is a narrow range of chloride concentrations over which this strain is most fit, and within which toxicity test data are reliable.

  3. Chloride channels in stroke

    Institute of Scientific and Technical Information of China (English)

    Ya-ping ZHANG; Hao ZHANG; Dayue Darrel DUAN

    2013-01-01

    Vascular remodeling of cerebral arterioles,including proliferation,migration,and apoptosis of vascular smooth muscle cells (VSMCs),is the major cause of changes in the cross-sectional area and diameter of the arteries and sudden interruption of blood flow or hemorrhage in the brain,ie,stroke.Accumulating evidence strongly supports an important role for chloride (Clˉ) channels in vascular remodeling and stroke.At least three Clˉ channel genes are expressed in VSMCs:1) the TMEM16A (or Ano1),which may encode the calcium-activated Clˉ channels (CACCs); 2) the CLC-3 Clˉ channel and Clˉ/H+ antiporter,which is closely related to the volume-regulated Clˉ channels (VRCCs); and 3) the cystic fibrosis transmembrane conductance regulator (CFTR),which encodes the PKA-and PKC-activated Clˉ channels.Activation of the CACCs by agonist-induced increase in intracellular Ca2+ causes membrane depolarization,vasoconstriction,and inhibition of VSMC proliferation.Activation of VRCCs by cell volume increase or membrane stretch promotes the production of reactive oxygen species,induces proliferation and inhibits apoptosis of VSMCs.Activation of CFTR inhibits oxidative stress and may prevent the development of hypertension.In addition,Clˉ current mediated by gammaaminobutyric acid (GABA) receptor has also been implicated a role in ischemic neuron death.This review focuses on the functional roles of Clˉ channels in the development of stroke and provides a perspective on the future directions for research and the potential to develop Clˉ channels as new targets for the prevention and treatment of stroke.

  4. 21 CFR 184.1138 - Ammonium chloride.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium chloride. 184.1138 Section 184.1138 Food... Specific Substances Affirmed as GRAS § 184.1138 Ammonium chloride. (a) Ammonium chloride (NH4Cl, CAS Reg. No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution....

  5. Cinchonidinium chloride monohydrate

    Directory of Open Access Journals (Sweden)

    Shi-Feng Ni

    2008-01-01

    Full Text Available In the title salt, C19H23N2O+·Cl−·H2O, the ions and the water molecule are held together by O—H...Cl, N—H...Cl, O—H...O, O—H...N and C—H...Cl hydrogen bonds, forming a three-dimensional framework. The vinyl group is disordered over two orientations with refined occupancies of 0.564 (16 and 0.436 (16. The cell parameters of the title compound have been reported previously [Griffiths (1952. Acta Cryst. 5, 290–291].

  6. Regulated trafficking of the CFTR chloride channel.

    Science.gov (United States)

    Kleizen, B; Braakman, I; de Jonge, H R

    2000-08-01

    The cystic fibrosis transmembrane conductance regulator (CFTR), the ABC transporter encoded by the cystic fibrosis gene, is localized in the apical membrane of epithelial cells where it functions as a cyclic AMP-regulated chloride channel and as a regulator of other ion channels and transporters. Whereas a key role of cAMP-dependent phosphorylation in CFTR-channel gating has been firmly established, more recent studies have provided clear evidence for the existence of a second level of cAMP regulation, i.e. the exocytotic recruitment of CFFR to the plasma membrane and its endocytotic retrieval. Regulated trafficking of the CFTR Cl- channel has sofar been demonstrated only in a subset of CFTR-expressing cell types. However, with the introduction of more sensitive methods to measure CFTR cycling and submembrane localization, it might turn out to be a more general phenomenon that could contribute importantly to both the regulation of CFTR-mediated chloride transport itself and to the regulation of other transporters and CFTR-modulated cellular functions. This review aims to summarize the present state of knowledge regarding polarized and regulated CFTR trafficking and endosomal recycling in epithelial cells, to discuss present gaps in our understanding of these processes at the cellular and molecular level, and to consider its possible implications for cystic fibrosis.

  7. Genetically encoded optical sensors for monitoring of intracellular chloride and chloride-selective channel activity

    Directory of Open Access Journals (Sweden)

    Piotr Bregestovski

    2009-12-01

    Full Text Available This review briefly discusses the main approaches for monitoring chloride (Cl−, the most abundant physiological anion. Noninvasive monitoring of intracellular Cl− ([Cl−]i is a challenging task owing to two main difficulties: (i the low transmembrane ratio for Cl−, approximately 10:1; and (ii the small driving force for Cl−, as the Cl− reversal potential (ECl is usually close to the resting potential of the cells. Thus, for reliable monitoring of intracellular Cl−, one has to use highly sensitive probes. From several methods for intracellular Cl− analysis, genetically encoded chloride indicators represent the most promising tools. Recent achievements in the development of genetically encoded chloride probes are based on the fact that yellow fluorescent protein (YFP exhibits Cl−-sensitivity. YFP-based probes have been successfully used for quantitative analysis of Cl− transport in different cells and for high-throughput screening of modulators of Cl−-selective channels. Development of a ratiometric genetically encoded probe, Clomeleon, has provided a tool for noninvasive estimation of intracellular Cl− concentrations. While the sensitivity of this protein to Cl− is low (EC50 about 160 mM, it has been successfully used for monitoring intracellular Cl− in different cell types. Recently a CFP–YFP-based probe with a relatively high sensitivity to Cl− (EC50 about 30 mM has been developed. This construct, termed Cl-Sensor, allows ratiometric monitoring using the fluorescence excitation ratio. Of particular interest are genetically encoded probes for monitoring of ion channel distribution and activity. A new molecular probe has been constructed by introducing into the cytoplasmic domain of the Cl−-selective glycine receptor (GlyR channel the CFP–YFP-based Cl-Sensor. This construct, termed BioSensor-GlyR, has been successfully expressed in cell lines. The new genetically encoded chloride probes offer means of screening

  8. 46 CFR 151.50-34 - Vinyl chloride (vinyl chloride monomer).

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Vinyl chloride (vinyl chloride monomer). 151.50-34... chloride (vinyl chloride monomer). (a) Copper, aluminum, magnesium, mercury, silver, and their alloys shall... equipment that may come in contact with vinyl chloride liquid or vapor. (b) Valves, flanges, and...

  9. 40 CFR 61.65 - Emission standard for ethylene dichloride, vinyl chloride and polyvinyl chloride plants.

    Science.gov (United States)

    2010-07-01

    ... dichloride, vinyl chloride and polyvinyl chloride plants. 61.65 Section 61.65 Protection of Environment... AIR POLLUTANTS National Emission Standard for Vinyl Chloride § 61.65 Emission standard for ethylene dichloride, vinyl chloride and polyvinyl chloride plants. An owner or operator of an ethylene...

  10. The need of alkalinity determination in the characterization of rain; Necesidad de la determinacion de la alcalinidad en la caracterizacion de la lluvia

    Energy Technology Data Exchange (ETDEWEB)

    Pal Verma, Mahendra [Instituto de Investigaciones Electricas, Cuernavaca (Mexico)

    1998-01-01

    In this paper is presented the alkalinity determination of the carbonic species in the rain waters by the Gran titration method. The alkalinity values obtained by this method in low electric conductivity waters are fairly reliable. Also, the existing studies on the characterization of acid rains, are discussed. [Espanol] En este trabajo se presenta la medicion de la alcalinidad y la determinacion de las especies carbonicas en las aguas de lluvia por el metodo de la titulacion de Gran. Los valores de alcalinidad obtenidos por este metodo en las aguas de baja conductividad electrica son bastante confiables. Asimismo, se discuten los estudios existentes sobre la caracterizacion de la lluvia acida en la republica mexicana.

  11. Simulation of an anion in water: effect of ion polarizability

    Science.gov (United States)

    Karim, Omar A.

    1991-10-01

    A polarizable-polar water model is used to study the structure of wate near a chloride ion. A semi-classical description of ion polarizability is included. Significant changes in the solute-solvent distribution functions are observed. When compared with a simulation without ion polarizability, it is found that the hydration number is further decreased when ion polarizability is present.

  12. Effect of NGBFS and CBA as fine aggregate on the chloride permeability of concrete

    Directory of Open Access Journals (Sweden)

    İsa Yüksel

    2013-09-01

    Full Text Available This paper presents the results of an investigation which was about influence of non-ground Coal Bottom Ash (CBA and Non-Ground Granulated Blast-Furnace Slag (NGBFS as fine aggregate on rapid chloride permeability of concrete. Series of Rapid Chloride Permeability Test (RCPT were conducted with concrete specimens containing NGBFS and CBA in varying percentages from 10 to 50% with the step of 10% of fine aggregate by weight. Two basic series concrete specimens were prepared in laboratory. The first series (G was contained NGBFS, the second series (B was contained CBA as fine aggregate. Test results indicated that NGBFS or CBA improves the resistance to chloride ion penetration tosome extent. 30% and 10% replacement ratios were selected as optimum replacement ratios for G and B series. It was concluded that GBFS was more impressive then CBA for blocking chloride ion movements.

  13. Prediction of the Service Life of a Reinforced Concrete Column under Chloride Environment

    Directory of Open Access Journals (Sweden)

    Mohammad K. Alkam

    2015-01-01

    Full Text Available In the present investigation, service life of a reinforced concrete column exposed to chloride environment has been predicted. This study has been based on numerical simulation of chloride ion diffusion in a concrete column during its anticipated life span. The simulation process has included the concrete cover replacement whenever chloride ion concentration has reached the critical threshold value at the reinforcement surface. Repair scheduling of the concrete column under consideration has been discussed. Effects of the concrete cover thickness and the water cement ratio on the service life of the concrete column at hand have been presented. A new approach for arranging locations of reinforcement steel bars has been introduced. This approach is intended to prolong the service life of the concrete column under consideration against chloride induced corrosion.

  14. Estimating the chloride transport in cement paste

    Directory of Open Access Journals (Sweden)

    Princigallo, A.

    2012-06-01

    Full Text Available A method was developed to measure the diffusion coefficient of chloride ions in cement paste based on an analytical solution to Fick’s 2nd law in a cylindrical coordinate system. This natural method yielded diffusivity results within as little as a month. Testing time was reduced by exploiting the three-dimensional inward flux in the specimen. In an attempt to determine the saturation concentration, dense portland cement pastes were exposed to a concentrated chloride solution. The method proved to be useful for exploring cement hydration-induced changes in the diffusion coefficient of cement paste.

    Se ha desarrollado un método para medir el coeficiente de difusión de los iones cloruro en la pasta de cemento, partiendo de una aplicación analítica de la segunda ley de Fick en un sistema de coordinadas cilíndrico. Este método, que es natural, demostró ser capaz de producir resultados de difusividad en tan solo un mes. Se consiguió reducir el tiempo de ensayo mediante el aprovechamiento de la tridimensionalidad del flujo desde el exterior al interior de la probeta. A fin de determinar la concentración de saturación, se sometieron las pastas de cemento Portland a una disolución de cloruros concentrada. Este método resultó ser útil en el estudio de los cambios del coeficiente de difusión de la pasta de cemento provocados por las reacciones de hidratación que tienen lugar en esta.

  15. Determination of Pu in soil samples; Determinacion de Pu en muestras de suelo

    Energy Technology Data Exchange (ETDEWEB)

    Torres C, C. O.; Hernandez M, H.; Romero G, E. T. [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico); Vega C, H. R., E-mail: carioli_32907@hotmail.com [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas, Zac. (Mexico)

    2016-10-15

    The irreversible consequences of accidents occurring in nuclear plants and in nuclear fuel reprocessing sites are mainly the distribution of different radionuclides in different matrices such as the soil. The distribution in the superficial soil is related to the internal and external exposure to the radiation of the affected population. The internal contamination with radionuclides such as Pu is of great relevance to the nuclear forensic science, where is important to know the chemical and isotopic compositions of nuclear materials. The objective of this work is to optimize the radiochemical separation of plutonium (Pu) from soil samples and to determine their concentration. The soil samples were prepared using acid digestion assisted by microwave; purification of Pu was carried out with AG1X8 resin using ion exchange chromatography. Pu isotopes were measured using ICP-SFMS. In order to reduce the interference due to the presence of {sup 238}UH {sup +} in the samples, a solvent removal system (Apex) was used. In addition, the limit of detection and quantification of Pu was determined. It was found that the recovery efficiency of Pu in soil samples ranges from 70 to 93%. (Author)

  16. Pourbaix diagrams of actinides in molten chlorides using an indicating electrode for oxide ion activity; Etablissement de diagrammes de Pourbaix des actinides dans les chlorures fondus au moyen d'une electrode indicatrice de l'activite des ions oxyde

    Energy Technology Data Exchange (ETDEWEB)

    Lambertin, D.; Lacquement, J. [CEA Valrho, (DCC/DRRV/SPHA), 30 - Marcoule (France)

    2000-07-01

    Pyrochemical separation methods using high temperature molten salt media could emerge as promising and valuable routes compared with aqueous methods for separation and transmutation strategies for long-lived radionuclides. A good knowledge of the molten salt chemistry is essential for controlling these separations, and elementary data are required for molten halide salts, which can be readily provided by electrochemical methods. Applying the chemical principles of aqueous solutions to the molten salt media, Pourbaix diagrams - called in this case potential-oxo-acidity (pO{sup 2-}) - can be plotted. They offer a rapid and comprehensive view of the thermodynamic properties of selected elements in a solvent of interest. Two methods are available for preparing these diagrams. The first is based on available thermodynamic data on pure element oxide (and oxychloride) compounds and on element chloride activity coefficients in melt (which can be electrochemically determined). In this method, we consider the oxide anion exchange reactions between the pure compounds, water and hydrogen chloride. The second method is a direct and experimental determination of the oxo-acidic properties of the studied element chlorides in melts. Use of an Yttria-Stabilised Zirconia Membrane (YSZM) electrode (oxide anion selective electrode) helps determine the nature of the stable oxide compounds in melts as well as their stabilities. The YSZM is used with a silver/silver chloride reference system, and was developed 25 years ago. Two examples of Potential-acidity diagrams. Employing the first method and the determination of the standard potential of plutonium in LiCl-KCl and NaCl-KCl eutectic mixtures, potential-oxo-acidity diagrams were plotted for these melts at various temperatures. It was found that the stability domain for plutonium chloride depends on the melt composition (influence of oxide anion solvation). We also used the Omega acidity function - based on reaction (1) - which is a

  17. Effect of Chloride Content on Bond Behavior Between FRP and Concrete

    Institute of Scientific and Technical Information of China (English)

    潘金龙; 黄毅方; 邢锋

    2010-01-01

    For reinforced concrete structures located along the seaside, the penetration of chloride ions into concrete may be a threat to the durability of the structures. Experimental investigations were carried out to study the effect of chloride content on the bond behavior between concrete and fiber reinforced polymer (FRP) plates. Direct shear tests were conducted on the FRP strengthened concrete members. Before testing, the specimens were immersed in NaCl solutions with concentrations ranging from 3%—15% for di...

  18. The influence of plasma protein concentration on potassium,sodium and chloride measurement by ion-selective-electrodes%血浆蛋白水平对间接离子选择电极法检测钾钠氯离子的影响

    Institute of Scientific and Technical Information of China (English)

    王志勇; 肖鹿骋; 顾桂兰; 曹娟; 张超; 盛敏

    2011-01-01

    目的 探讨血浆蛋白水平变化导致间接和直接离子选择电极法(ISE)结果间存在的差异,揭示直接ISE与间接ISE测定血浆钾、钠、氯离子结果之间的差异与血浆蛋白水平之间的关系.方法 选取低、中、高血浆蛋白的独立样本,研究直接与间接离子选择电极法对血浆钾、钠、氯检测结果差异以及与蛋白水平之间的线性关系.结果 间接法与直接法检测钠离子结果差异有统计学意义(P<0.05),钠离子结果差异与总蛋白、清蛋白离子回归方程分别为Y=-0.129 4X+9.604 1和Y=-0.195X+7.807 8,相关系数r(r2)分别为0.76(0.57)和0.61(0.37),均P<0.001.结论 采用间接ISE法检测血浆钠离子时,对血浆蛋白水平的变化具有影响,直接与间接ISE法检测血浆钠离子结果差异和总蛋白、白蛋白水平之间线性回归等式可以成立.在总蛋白和(或)清蛋白水平明显异常时,直接ISE法测定血浆钠离子结果应当作为临床正确的依据.%Objective To test the hypothesis that the difference between indirect and direct potassium, sodium and chloride assays would be related to the plasma protein concentration, and to derive the relationship between the difference of direct and indirect ion selective electrode(ISE) measurements of plasma potassium,sodium and chloride and the protein concentration. Methods Independent specimens,that covered the whole level of the protein range, were selected,and linear relationships between the difference between direct and indirect ISE measurements of plasma potassium,sodium,chloride and the total protein and albumin concentration were analyzed. Results Significant biases were observed between indirect and direct ISE measurement of sodium level. The regression equations of the difference and the total protein level, albumin level were Y= - 0. 129 4X + 9. 604 1 和 Y = - 0. 195X + 7. 807 8, with r(r2 )of 0. 76(0. 57)and 0. 61(0. 37)and with P<0. 001. Conclusion The plasma sodium

  19. Indirect Determination of Perchloric Ion in Diethydiprydine Perchlorate by ICP-AES with Tetraphenylphosphonium Chloride as Precipitation Reagent%ICP-AES 法间接测定高氯酸二乙基联吡啶中的高氯酸根

    Institute of Scientific and Technical Information of China (English)

    刘永明; 李桂芝

    2001-01-01

    A method for indirect determination of perchloric ion by ICP-AESwas studied and optimal conditions were selected. The perchloric ion in insoluble diethydiprydine perchlorate sample was reacted with excessive tetraphenylphosphonium chloride(TTPC) and converted to TPPClO4 in filtrate and was then detected by ICP-AES. This method was used for analysis of ClO4- in diethydiprydine perchlorate with RSD of 0.74% and recovery of 97.3%~100.6%. The obtained results were consistent with those by gravimetric method.%研究了ICP-AES法间接测定高氯酸二乙基联吡啶中高氯酸根含量的方法。选择了氯化四苯(TPPCl)与高氯酸根发生沉淀的条件及ICP-AES测定氯化四苯的最佳条件。在氯化四苯过量的情况下,在水中难溶的高氯酸二乙基联吡啶可以定量转化成TPPClO4晶形沉淀。通过测定反应剩余的TPPCl,可计算得到样品中高氯酸根的含量。方法的相对标准偏差0.74%,回收率99.5%~100.6%。同时以TPPCl为沉淀剂,用重量法测定了样品中高氯酸根含量,结果与ICP-AES法一致。

  20. Determination of Tc-99 in radioactive wastes; Determinacion de Tc-99 en desechos radiactivos

    Energy Technology Data Exchange (ETDEWEB)

    Rivera S, A. A.

    2015-07-01

    Tc-99 is a fission product and one of the most important radionuclides from the view point of safety assessment for the disposal of radioactive waste because of its long half-life (2.1 x 10{sup 5} years) and high mobility in soil-water systems, if this is released into the environment in significant quantities can concentrate on plants and animals. Tc-99 is a pure beta emitter with a maximum energy of 292 KeV, so their quantification imposes destructive methods to be analyzed by liquid scintillation. Therefore the quantification of Tc-99 in ion exchange resins requires of the mineralization of these and separation of Tc-99 of other radioisotopes present in the resin. Therefore the object of this thesis is to develop a quantification method of Tc-99 content in spent exchange resins. So in order to track the behavior of technetium during digestion exchange resins and radiochemical separation, given its high volatility, in this work the {sup 99m}Tc is used. To determine the degree of mineralization of the resins, an analysis was performed by chromatography. Subsequently the method used to determine the percentage of {sup 99m}Tc aerosolized during mineralization of resin is described. After the method for the radiochemical separation of {sup 99m}Tc is presented by liquid-liquid extraction using crown ether as extractant; for this testing was performed by varying the molarity of the extractant, the ratio of solvent extractant, type of digestion of the resin and the presence of Sr-85, in order to study the behavior of {sup 99m}Tc in the presence of this radioisotope. Finally, a track beta spectra of a sample of {sup 99m}Tc eluted from a generator {sup 99}Mo/{sup 99m}Tc function of time was performed. (Author)

  1. Solid-phase extraction of cobalt(II) from lithium chloride solutions using a poly(vinyl chloride)-based polymer inclusion membrane with Aliquat 336 as the carrier.

    Science.gov (United States)

    Kagaya, Shigehiro; Cattrall, Robert W; Kolev, Spas D

    2011-01-01

    The extraction of cobalt(II) from solutions containing various concentrations of lithium chloride, hydrochloric acid, and mixtures of lithium chloride plus hydrochloric acid is reported using a poly(vinyl chloride) (PVC)-based polymer inclusion membrane (PIM) containing 40% (w/w) Aliquat 336 as a carrier. The extraction from lithium chloride solutions and mixtures with hydrochloric acid is shown to be more effective than extraction from hydrochloric acid solutions alone. The solution concentrations giving the highest amounts of extraction are 7 mol L(-1) for lithium chloride and 8 mol L(-1) lithium chloride plus 1 mol L(-1) hydrochloric acid for mixed solutions. Cobalt(II) is easily stripped from the membrane using deionized water. The cobalt(II) species extracted into the membrane are CoCl(4)(2-) for lithium chloride solutions and HCoCl(4)(-) for mixed solutions; these form ion-pairs with Aliquat 336. It is also shown that both lithium chloride and hydrochloric acid are extracted by the PIM and suppress the extraction of cobalt(II) by forming ion-pairs in the membrane (i.e. R(3)MeN(+)·HCl(2)(-) for hydrochloric acid and R(3)MeN(+)·LiCl(2)(-) for lithium chloride).

  2. Suppression of adenosine-activated chloride transport by ethanol in airway epithelia.

    Directory of Open Access Journals (Sweden)

    Sammeta V Raju

    Full Text Available Alcohol abuse is associated with increased lung infections. Molecular understanding of the underlying mechanisms is not complete. Airway epithelial ion transport regulates the homeostasis of airway surface liquid, essential for airway mucosal immunity and lung host defense. Here, air-liquid interface cultures of Calu-3 epithelial cells were basolaterally exposed to physiologically relevant concentrations of ethanol (0, 25, 50 and 100 mM for 24 hours and adenosine-stimulated ion transport was measured by Ussing chamber. The ethanol exposure reduced the epithelial short-circuit currents (I(SC in a dose-dependent manner. The ion currents activated by adenosine were chloride conductance mediated by cystic fibrosis transmembrane conductance regulator (CFTR, a cAMP-activated chloride channel. Alloxazine, a specific inhibitor for A(2B adenosine receptor (A(2BAR, largely abolished the adenosine-stimulated chloride transport, suggesting that A(2BAR is a major receptor responsible for regulating the chloride transport of the cells. Ethanol significantly reduced intracellular cAMP production upon adenosine stimulation. Moreover, ethanol-suppression of the chloride secretion was able to be restored by cAMP analogs or by inhibitors to block cAMP degradation. These results imply that ethanol exposure dysregulates CFTR-mediated chloride transport in airways by suppression of adenosine-A(2BAR-cAMP signaling pathway, which might contribute to alcohol-associated lung infections.

  3. Electrochemical Chloride extraction using external electrodes?

    DEFF Research Database (Denmark)

    Ottosen, Lisbeth M.; Pedersen, Anne Juul

    2006-01-01

    Electrochemical methods for the removal of chloride from concrete have been developed and the methods are primarily designed for situations where corrosion has started due to an increased chloride concentration in the vicinity of the reinforcement. In these methods the reinforcement is used...... as the cathode. However, some unwanted side effects can occur, including alkali-silica reaction and in some cases hydrogen embrittlement. It is also suggested also to use electrochemical chloride extraction in a preventive way in constructions where chloride induced corrosion is likely to be a problem after...... a period of time, i.e. remove the chlorides before the chloride front reaches the reinforcement. If the chlorides are removed from outer few centimetres from the surface, the chloride will not reach the reinforcement and cause damage. By using the electrochemical chloride removal in this preventive way...

  4. Two-and Three-Dimensional Chloride Ingress into Fly Ash Concrete

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yunsheng; SUN Wei; CHEN Shudong; GUO Fei

    2011-01-01

    2D,3D chloride ion concentration at the edge and comer zones were systematically investigated for fly ash concretes made with different cement replacement percentage by fly ash (0%,10%,20%,40%,60%),water to binder ratios (0.3,0.35,0.4),and curing ages (28 d,90 d).An interaction effect caused by 2D and 3D diffusion could obviously be observed through the comparison with 1D testing results.In order to quantify the interaction effect,2D and 3D diffusion interaction coefficients was proposed in this paper.Finally,the changes of 2D and 3D interaction coefficients with the change in the free chloride ion concentration were given.The above research provide an insight into chloride ion attack on the edge and comer reinforcing bars of concrete structures in the field of civil engineering.

  5. Lubiprostone: a chloride channel activator.

    Science.gov (United States)

    Lacy, Brian E; Levy, L Campbell

    2007-04-01

    In January 2006 the Food and Drug Administration approved lubiprostone for the treatment of chronic constipation in men and women aged 18 and over. Lubiprostone is categorized as a prostone, a bicyclic fatty acid metabolite of prostaglandin E1. Lubiprostone activates a specific chloride channel (ClC-2) in the gastrointestinal (GI) tract to enhance intestinal fluid secretion, which increases GI transit and improves symptoms of constipation. This article reviews the role of chloride channels in the GI tract, describes the structure, function, and pharmacokinetics of lubiprostone, and discusses clinically important data on this new medication.

  6. Chloride content and pH value in the pore solution of concrete under carbonation

    Institute of Scientific and Technical Information of China (English)

    Xiao-mei WAN; Folker H.WITTMANN; Tie-jun ZHAO; Hong FAN

    2013-01-01

    Chloride content and the pH value of the pore solution in the neighborhood of steel reinforcement are decisive parameters for initiation and rate of corrosion.The pore solution of cement mortar and hardened cement paste has been expressed from the pore space by high pressure in the investigation.The influence of the water-cement ratio,age,and addition of chloride to the fresh mix on chloride content in the pore solution has been determined by ion chromatography.At the same time the pH value of the pore solution has been determined.The dissolved chloride content decreases with increase in the water-cement ratio.The amount of bound chloride increases with time,but it decreases with decreasing content of dissolved chloride in the pore solution.A significant influence of carbonation on the dissolved chloride content of the pore solution has been observed.With complete carbonation,the dissolved chloride content in cement mortar and hardened cement paste increases by a factor between 2 and 12.The bound chloride decreases by 27%-54%.As expected,the pH value decreases from around 13.2 to as low as 8.0 due to carbonation.It can be concluded that carbonation not only lowers the pH value but liberates bound chloride.This is one obvious reason why the combined action of chloride penetration and carbonation accelerates steel corrosion and shortens the service life of reinforced concrete structures.

  7. Resistance of Alkali-Activated Slag Concrete to Chloride-Induced Corrosion

    Directory of Open Access Journals (Sweden)

    Joon Woo Park

    2015-01-01

    Full Text Available The corrosion resistance of steel in alkali-activated slag (AAS mortar was evaluated by a monitoring of the galvanic current and half-cell potential with time against a chloride-contaminated environment. For chloride transport, rapid chloride penetration test was performed, and chloride binding capacity of AAS was evaluated at a given chloride. The mortar/paste specimens were manufactured with ground granulated blast-furnace slag, instead of Portland cement, and alkali activators were added in mixing water, including Ca(OH2, KOH and NaOH, to activate hydration process. As a result, it was found that the corrosion behavior was strongly dependent on the type of alkali activator: the AAS containing the Ca(OH2 activator was the most passive in monitoring of the galvanic corrosion and half-cell potential, while KOH, and NaOH activators indicated a similar level of corrosion to Portland cement mortar (control. Despite a lower binding of chloride ions in the paste, the AAS had quite a higher resistance to chloride transport in rapid chloride penetration, presumably due to the lower level of capillary pores, which was ensured by the pore distribution of AAS mortar in mercury intrusion porosimetry.

  8. [Headspace GC/MS analysis of residual vinyl chloride and vinylidene chloride in polyvinyl chloride and polyvinylidene chloride products].

    Science.gov (United States)

    Ohno, Hiroyuki; Mutsuga, Motoh; Kawamura, Yoko; Suzuki, Masako; Aoyama, Taiki

    2005-02-01

    A headspace GC/MS analysis method for the simultaneous determination of residual vinyl chloride (VC) and vinylidene chloride (VDC) in polyvinyl chloride (PVC) and polyvinylidene chloride (PVDC) products was developed. A test sample was swelled overnight with N,N-dimethylacetamide in a sealed vial. The vial was incubated for 1 hour at 90 degrees C, then the headspace gas was analyzed by GC/MS using a PLOT capillary column. The recoveries from spiked PVC and PVDC samples were 90.0-112.3% for VC and 85.2-108.3% for VDC. The determination limits were 0.01 microg/g for VC and 0.06/microg/g for VDC, respectively. By this method, VC was detected in two PVC water supply pipes at the levels of 0.61 and 0.01 microg/g. On the other hand, VC and VDC were not detected in any of the food container-packages or toys tested.

  9. 1,5-Diaminotetrazolium chloride

    Directory of Open Access Journals (Sweden)

    Ling-Qiao Meng

    2010-04-01

    Full Text Available The title compound, CH5N6+·Cl−, crystallized with two indepedent 1,5-diaminotetrazolium cations and two independent chloride anions in the asymmetric unit. In the crystal, there are a number of N—H...Cl hydrogen-bonding interactions, which generate a three-dimensional network.

  10. Chloride diffusivity in hardened cement paste from microscale analyses and accounting for binding effects

    Science.gov (United States)

    Carrara, P.; De Lorenzis, L.; Bentz, D. P.

    2016-08-01

    The diffusion of chloride ions in hardened cement paste (HCP) under steady-state conditions and accounting for the highly heterogeneous nature of the material is investigated. The three-dimensional HCP microstructures are obtained through segmentation of x-ray images of real samples as well as from simulations using the cement hydration model CEMHYD3D. Moreover, the physical and chemical interactions between chloride ions and HCP phases (binding), along with their effects on the diffusive process, are explicitly taken into account. The homogenized diffusivity of the HCP is then derived through a least square homogenization technique. Comparisons between numerical results and experimental data from the literature are presented.

  11. 21 CFR 173.375 - Cetylpyridinium chloride.

    Science.gov (United States)

    2010-04-01

    ... CONSUMPTION Specific Usage Additives § 173.375 Cetylpyridinium chloride. Cetylpyridinium chloride (CAS Reg. No... Nutrition's Library, Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, or...

  12. Microbial reductive dehalogenation of vinyl chloride

    Energy Technology Data Exchange (ETDEWEB)

    Spormann, Alfred M [Stanford, CA; Muller, Jochen A [Baltimore, MD; Rosner, Bettina M [Berlin, DE; Von Abendroth, Gregory [Mannheim, DE; Meshulam-Simon, Galit [Los Angeles, CA; McCarty, Perry L [Stanford, CA

    2014-02-11

    Compositions and methods are provided that relate to the bioremediation of chlorinated ethenes, particularly the bioremediation of vinyl chloride by Dehalococcoides-like organisms. An isolated strain of bacteria, Dehalococcoides sp. strain VS, that metabolizes vinyl chloride is provided; the genetic sequence of the enzyme responsible for vinyl chloride dehalogenation; methods of assessing the capability of endogenous organisms at an environmental site to metabolize vinyl chloride; and a method of using the strains of the invention for bioremediation.

  13. Sugar-metal ion interactions: The coordination behavior of cesium ion with lactose, D-arabinose and L-arabinose

    Science.gov (United States)

    Jiang, Ye; Xue, Junhui; Wen, Xiaodong; Zhai, Yanjun; Yang, Limin; Xu, Yizhuang; Zhao, Guozhong; Kou, Kuan; Liu, Kexin; Chen, Jia'er; Wu, Jinguang

    2016-04-01

    The novel cesium chloride-lactose complex (CsCl·C12H22O10 (Cs-Lac), cesium chloride-D-arabinose and L-arabinose complexes (CsCl·C5H10O5, Cs-D-Ara and Cs-L-Ara) have been synthesized and characterized using X-ray diffraction, FTIR, FIR, THz and Raman spectroscopies. Cs+ is 9-coordinated to two chloride ions and seven hydroxyl groups from five lactose molecules in Cs-Lac. In the structures of CsCl-D-arabinose and CsCl-L-arabinose complexes, two kinds of Cs+ ions coexist in the structures. Cs1 is 10-coordinated with two chloride ions and eight hydroxyl groups from five arabinose molecule; Cs2 is 9-coordinated to three chloride ions and six hydroxyl groups from five arabinose molecules. Two coordination modes of arabinose coexist in the structures. α-D-arabinopyranose and α-L-arabinopyranose appear in the structures of Cs-D-Ara and Cs-L-Ara complexes. FTIR and Raman results indicate variations of hydrogen bonds and the conformation of the ligands after complexation. FIR and THz spectra also confirm the formation of Cs-complexes. Crystal structure, FTIR, FIR, THz and Raman spectra provide detailed information on the structure and coordination of hydroxyl groups to metal ions in the cesium chloride-lactose, cesium chloride-D- and L-arabinose complexes.

  14. Ion transport across transmembrane pores

    NARCIS (Netherlands)

    Leontiadou, Hari; Mark, Alan E.; Marrink, Siewert-Jan

    2007-01-01

    To study the pore-mediated transport of ionic species across a lipid membrane, a series of molecular dynamics simulations have been performed of a dipalmitoyl-phosphatidyl-choline bilayer containing a preformed water pore in the presence of sodium and chloride ions. It is found that the stability of

  15. 21 CFR 184.1426 - Magnesium chloride.

    Science.gov (United States)

    2010-04-01

    ... mineral bischofite. It is prepared by dissolving magnesium oxide, hydroxide, or carbonate in aqueous... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Magnesium chloride. 184.1426 Section 184.1426 Food... Specific Substances Affirmed as GRAS § 184.1426 Magnesium chloride. (a) Magnesium chloride (MgC12·6H2O,...

  16. Cystic Fibrosis (CF): Chloride Sweat Test

    Science.gov (United States)

    ... Old Feeding Your 1- to 2-Year-Old Cystic Fibrosis (CF) Chloride Sweat Test KidsHealth > For Parents > Cystic Fibrosis (CF) Chloride Sweat Test Print A A A ... It Is A chloride sweat test helps diagnose cystic fibrosis (CF) , an inherited disorder that makes kids sick ...

  17. 75 FR 33824 - Barium Chloride From China

    Science.gov (United States)

    2010-06-15

    ... COMMISSION Barium Chloride From China Determination On the basis of the record\\1\\ developed in the subject... order on barium chloride from China would be likely to lead to continuation or recurrence of material... Barium Chloride from China: Investigation No. 731-TA-149 (Third Review). By order of the...

  18. 75 FR 19657 - Barium Chloride From China

    Science.gov (United States)

    2010-04-15

    ... COMMISSION Barium Chloride From China AGENCY: United States International Trade Commission. ACTION: Notice of... chloride from China. SUMMARY: The Commission hereby gives notice that it will proceed with a full review... revocation of the antidumping duty order on barium chloride from China would be likely to lead...

  19. 21 CFR 172.180 - Stannous chloride.

    Science.gov (United States)

    2010-04-01

    ... Preservatives § 172.180 Stannous chloride. The food additive stannous chloride may be safely used for color... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Stannous chloride. 172.180 Section 172.180 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR...

  20. Research on Regulating and Controlling Roles of Chloride and Zinc Ions to Swine Sperm Calcium Channel and Some Enzyme Activities%氯、锌离子对猪精子钙通道和若干酶活调控作用的研究

    Institute of Scientific and Technical Information of China (English)

    周明; 刘芳芳; 李晓东; 邢立东; 吴金节; 解正会; 郭森

    2012-01-01

    The regulating and controlling roles of chloride and zinc ions to swine sperm calcium channel and their mechanism were studied.Semen from healthy boar were filtered with gauze and divided into three groups,each group having 6 repeats.The group 1 semen was not added anything;the group 2 and 3 semen were added NaCl and ZnSO 4 solution respectively.Being mixed and placed 2.5 h,various parameters of 3 experimental semen were measured.Experimental results showed that:(1) supplementation of optimum chlorine ions or zinc ions in semen could stimulate migration of calcium ions from Seminal plasm to sperm,thus calcium ion concentration in sperm raised significantly(P 〈 0.05),calcium ion concentration in Seminal plasm decreasesd slightly;(2) supplementation of chlorine or zinc ions in semen could strengthen sperm motility highly significantly(P 〈 0.01);(3) after supplementation of zinc ions in semen,the activities of AKP,CA and AC and the concentration of cAMP in sperm increased highly significantly(P 〈 0.01),the activities of AKP and AC in seminal plasm raised highly significantly(P 〈 0.01),the concentration of cAMP in seminal plasm increased significantly(P 〈 0.05);(4) after supplementation of chlorine ions in semen,the activities of AKP and AC in seminal plasm raised highly significantly(P 〈 0.01),the concentration of cAMP in Seminal l plasm increased significantly(P 〉 0.05).These results suggested that supplementation of optimum zinc or chlorine ions in boar semen may up-regulate the function of sperm calcium channel,and can improve the activities of AKP,CA and AC and the concentration of cAMP in semen,strengthen sperm motility.%研究了氯离子、锌离子等对猪精子钙通道的调控作用及其机理。将由健康公猪采得的精液经纱布过滤后分为3组,每组6个重复。第1组精液不加任何物质,第2、3组精液分别加氯化钠液和硫酸锌液,混匀并静置2.5h后,观测精子

  1. Formation of La{sup 3+}, Pr{sup 3+}, Eu{sup 3+}, Er{sup 3+}, and Lu{sup 3+} complexes with chloride ions, in aqueous medium; Formacion de complejos de La{sup 3+}, Pr{sup 3+}, Eu{sup 3+}, Er{sup 3+} y Lu{sup 3+} con iones cloruro, en medio acuoso

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez R, E.; Jimenez R, M.; Solache R, M. [ININ, 52750 La Marquesa, Estado de Mexico (Mexico)

    2007-07-01

    The constants of stability of the complexes of La{sup 3+}, Pr{sup 3+}, Eu{sup 3+}, Er{sup 3+}, and Lu{sup 3+} with Cl{sup -} ions, its were determined, in the aqueous medium of HCI - HClO{sub 4} and by a solvent extraction method. The dinonyl naphtalene sulfonic acid in n-heptane was used as extractant. The lanthanides concentration, it was measured by a VIS spectrophotometry method and by another radiochemical. The ions specific interaction theory (SIT) it was used for the extrapolation to ionic force 0 M. The results indicate that the stability constants of the LnCI{sup 2+} species diminishes when increasing the ion force and the charge density. (Author)

  2. Spectrophotometric determination of fluorides in water with Hach equipment; Determinacion espectrofotometrica de fluoruros en aguas con equipo Hach

    Energy Technology Data Exchange (ETDEWEB)

    Acosta L, E. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)]. e-mail: eal@nuclear.inin.mx

    1994-11-15

    The spectrophotometric method for the determination of the fluoride ion in water, demineralized water, raw waters, laundry waters and waters treated with ion exchange resins , using the technique and the SPADNS coloring indicated in the operation manual of the Hach equipment is described. This method covers the determination of the fluoride ion in the range from 0 to 2 mg/l on 25 ml. of radioactive base sample. These limits can be variable if the size of the used aliquot one is changed for the final determination of the fluoride ion. (Author)

  3. Electrochemical synthesis and characterization of chloride doped polyaniline

    Indian Academy of Sciences (India)

    A M Pharhad Hussain; A Kumar

    2003-04-01

    Chloride doped polyaniline conducting polymer films have been prepared in a protic acid medium (HCl) by potentiodynamic method in an electrochemical cell and studied by cyclic voltammetry and FTIR techniques. The FTIR spectra confirmed Cl– ion doping in the polymers. The polymerization rate was found to increase with increasing concentration of aniline monomer. But the films obtained at high monomer concentration were rough having a nonuniform flaky polyaniline distribution. Results showed that the polymerization rate did not increase beyond a critical HCl concentration. Cyclic voltammetry suggested that, the oxidation-reduction current increased with an increase in scan rate and that the undoped polyaniline films were not hygroscopic whereas chloride doped polyaniline films were found to be highly hygroscopic.

  4. Chloride transport and its sensitivities to different boundary conditions in reclaimed soil solutions filled with fly ash

    Institute of Scientific and Technical Information of China (English)

    Xiao-Yang CHEN; Jia-Ping YAN; Shi-Wen ZHANG

    2013-01-01

    Chloride ion transport in reclaimed soil solutions filled with fly ash (FA) was investigated by measuring the hydraulic parameters (i.e.water retention curves and hydraulic conductivity) of three substrates,namely GSL,GFA,and CFA.Similar simulations were carried out under certain weather conditions.The different boundary conditions of chloride transport were also discussed from FA texture,cover soil thickness,groundwater table level,and initial chloride concentration.Furthcrmore,the sensitivities of chloride ions to these effect factors were analyzed.The results show that the different top soil thickness and initial chloride concentration have no effect on salinity of topsoil solution in the monitoring points,but they can clearly change the chloride concentration of FA layers.The sensibilities from top soil thickness and initial chloride content are exceedingly weak to the salinity balance based on two dimensions of the time and concentration.While the different FA texture and groundwater table not only affect the salinity equilibrium process of the whole reclaimed soil profile,but also change its balance state.Generally,coarse FA particles and high groundwater table can defer the salinity balance process of the reclaimed soil solution,and they also increase the chloride concentration of FA layer solutions,and even topsoil ones.

  5. Effect of Organic Inhibitors on Chloride Corrosion of Steel Rebars in Alkaline Pore Solution

    Directory of Open Access Journals (Sweden)

    Marina Cabrini

    2015-01-01

    Full Text Available The inhibition properties of aspartic and lactic acid salts are compared with nitrite ions with regard to their effect on critical chloride concentration. The tests were carried out on carbon steel specimens in simulated pore solutions with initial pH in the range of 12.6 to 13.8. The critical chloride concentrations were estimated through multiple specimen potentiostatic tests at potentials in the usual range for passive rebar in noncarbonated concrete structures. During tests, chloride ions were progressively added until all specimens showed localized attack, obtaining cumulative distribution curves reporting the fraction of corroded specimens as a function of chloride concentration. The presence of the organic inhibitors on the passivity film was detected by IR spectra. The results confirm that 0.1 M aspartate exhibits an inhibiting effect comparable with nitrite ions of the same concentration. Calcium lactate does not increase critical chloride concentration; however it appears to promote the formation of a massive scale, reducing the corrosion propagation.

  6. Specific ion effects on membrane potential and the permselectivity of ion exchange membranes

    KAUST Repository

    Geise, Geoffrey M.

    2014-08-26

    © the Partner Organisations 2014. Membrane potential and permselectivity are critical parameters for a variety of electrochemically-driven separation and energy technologies. An electric potential is developed when a membrane separates electrolyte solutions of different concentrations, and a permselective membrane allows specific species to be transported while restricting the passage of other species. Ion exchange membranes are commonly used in applications that require advanced ionic electrolytes and span technologies such as alkaline batteries to ammonium bicarbonate reverse electrodialysis, but membranes are often only characterized in sodium chloride solutions. Our goal in this work was to better understand membrane behaviour in aqueous ammonium bicarbonate, which is of interest for closed-loop energy generation processes. Here we characterized the permselectivity of four commercial ion exchange membranes in aqueous solutions of sodium chloride, ammonium chloride, sodium bicarbonate, and ammonium bicarbonate. This stepwise approach, using four different ions in aqueous solution, was used to better understand how these specific ions affect ion transport in ion exchange membranes. Characterization of cation and anion exchange membrane permselectivity, using these ions, is discussed from the perspective of the difference in the physical chemistry of the hydrated ions, along with an accompanying re-derivation and examination of the basic equations that describe membrane potential. In general, permselectivity was highest in sodium chloride and lowest in ammonium bicarbonate solutions, and the nature of both the counter- and co-ions appeared to influence measured permselectivity. The counter-ion type influences the binding affinity between counter-ions and polymer fixed charge groups, and higher binding affinity between fixed charge sites and counter-ions within the membrane decreases the effective membrane charge density. As a result permselectivity decreases. The

  7. Oxomemazine hydro­chloride

    OpenAIRE

    Siddegowda, M. S.; Butcher, Ray J.; Mehmet Akkurt; Yathirajan, H.S.; Ramesh, A. R.

    2011-01-01

    In the title compound [systematic name: 3-(5,5-dioxophenothiazin-10-yl)-N,N,2-trimethylpropanaminium chloride], C18H23N2O2S+·Cl−, the dihedral angle between the two outer aromatic rings of the phenothiazine unit is 30.5 (2)°. In the crystal, the components are linked by N—H...Cl and C—H...Cl hydrogen bonds and C—H...π interactions.

  8. Shock compression of polyvinyl chloride

    Science.gov (United States)

    Neogi, Anupam; Mitra, Nilanjan

    2016-04-01

    This study presents shock compression simulation of atactic polyvinyl chloride (PVC) using ab-initio and classical molecular dynamics. The manuscript also identifies the limits of applicability of classical molecular dynamics based shock compression simulation for PVC. The mechanism of bond dissociation under shock loading and its progression is demonstrated in this manuscript using the density functional theory based molecular dynamics simulations. The rate of dissociation of different bonds at different shock velocities is also presented in this manuscript.

  9. Effectiveness of inhibitors in increasing chloride threshold value for steel corrosion

    Directory of Open Access Journals (Sweden)

    Jin-xia XU

    2013-07-01

    Full Text Available This investigation was aimed at evaluating the effectiveness of corrosion inhibitors in increasing the chloride threshold value for steel corrosion. Three types of corrosion inhibitors, calcium nitrite (Ca(NO22, zinc oxide (ZnO, and N,N'-dimethylaminoethanol (DMEA, which respectively represented the anodic inhibitor, cathodic inhibitor, and mixed inhibitor, were chosen. The experiment was carried out in a saturated calcium hydroxide (Ca(OH2 solution to simulate the electrolytic environment of concrete. The inhibitors were initially mixed at different levels, and then chloride ions were gradually added into the solution in several steps. The open-circuit potential (Ecorr and corrosion current density (Icorr determined by electrochemical impedance spectra (EIS were used to identify the initiation of active corrosion, thereby determining the chloride threshold value. It was found that although all the inhibitors were effective in decreasing the corrosion rate of steel reinforcement, they had a marginal effect on increasing the chloride threshold value.

  10. Chloride diffusivity in red mud-ordinary portland cement concrete determined by migration tests

    Directory of Open Access Journals (Sweden)

    Daniel Véras Ribeiro

    2011-01-01

    Full Text Available Red mud, which is a solid waste produced in the alumina production process, is classified as dangerous due to its high pH. In this work, the concentration of chlorides was monitored by measuring the conductivity of the anolyte, which initially was distilled water. The steady and nonsteady-state chloride diffusion coefficients were estimated from the "time lag"� and "equivalent time" between diffusion and migration experiments. The capillary water absorption, apparent porosity and pore size distribution of concretes were also analyzed. The addition of red mud apparently ensured lower chloride diffusion in the tested mixtures due to its superfine particle-size distribution and its "filler"� effect. Red mud lengthened the service life of the concrete to 35 years (double that of the reference concrete. This finding is very positive since it indicates a delay in the onset of the rebar corrosion process caused by the migration of chloride ions.

  11. Developing chloride resisting concrete using PFA

    Energy Technology Data Exchange (ETDEWEB)

    Dhir, R.K.; El-Mohr, M.A.K.; Dyer, T.D. [Univ. of Dundee (United Kingdom). Dept. of Civil Engineering

    1997-11-01

    PFA concrete mixes were designed to optimize resistance to chloride ingress. Chloride binding capacity, intrinsic permeability and their concomitant influence on the coefficient of chloride diffusion have been investigated. PFA replacements up to 67% and exposure concentrations of 0.1, 0.5, 1.0 and 5.0 mole/liter were used. Chloride binding capacity was found to increase with increasing PFA replacement up to 50% and to then decline. It increased with chloride exposure concentration as well as water/binder ratio. The coefficient of chloride diffusion of concrete samples was found to be dependent on both the intrinsic permeability of the concrete and the ability of its cement matrix to bind chlorides.

  12. Salt, chloride, bleach, and innate host defense.

    Science.gov (United States)

    Wang, Guoshun; Nauseef, William M

    2015-08-01

    Salt provides 2 life-essential elements: sodium and chlorine. Chloride, the ionic form of chlorine, derived exclusively from dietary absorption and constituting the most abundant anion in the human body, plays critical roles in many vital physiologic functions, from fluid retention and secretion to osmotic maintenance and pH balance. However, an often overlooked role of chloride is its function in innate host defense against infection. Chloride serves as a substrate for the generation of the potent microbicide chlorine bleach by stimulated neutrophils and also contributes to regulation of ionic homeostasis for optimal antimicrobial activity within phagosomes. An inadequate supply of chloride to phagocytes and their phagosomes, such as in CF disease and other chloride channel disorders, severely compromises host defense against infection. We provide an overview of the roles that chloride plays in normal innate immunity, highlighting specific links between defective chloride channel function and failures in host defense.

  13. Comparison of different methods for determination of sodium chloride in cheese

    Directory of Open Access Journals (Sweden)

    Rajković Miloš B.

    2010-01-01

    Full Text Available The content of NaCl (weight fraction of Cl-ions, in % was analysed in different cheeses, which were bought in supermarkets, and made by domestic manufacturers. Sodium chloride in cheese samples was analysed after the extraction of chloride by nitric acid solution. Concentration of chloride ions was potentiometricly determined, with the chloride selective electrode and titrimetricly by Volhard method. According to the results in the analysis of the content of NaCl in %, by different methods it was determined that the share of NaCl in % ranged from 0.66 to 4.43% (determined by potentiometric route that is from 0.97 to 4.72% (determined by titrimetric route by Volhard method. The difference in received results in different methods is less if the share of NaCl, in % is higher than 3%. If the share is less than 3%, the difference in results rapidly increases, and the biggest difference is when the share is less than 1%. This analysis was done according to the results received by Volhard method, which is accepted as a standard method. As Volhard method is in connection with cheese resolving by intense oxidation means, azotic acid and potassium permanganate, obligatory in fume board (hood, it is not a practical method. On the other hand, the potentiometric method with usage of the chloride-selective electrode is very simple and gives reliable and reproductive results. In case of a small content of NaCl, in %, higher precision and accuracy of determination by chloride-selective electrode can be obtained by indirect measurement of chloride-ions (by standard addition method.

  14. Effect of Chlorides on Conductivity and Dielectric Constant in Hardened Cement Mortar: NDT for Durability Evaluation

    Directory of Open Access Journals (Sweden)

    Sunkook Kim

    2016-01-01

    Full Text Available Dielectric constant and conductivity, the so-called EM properties (electromagnetic, are widely adopted for NDT (Nondestructive Technique in order to detect damage or evaluate performance of concrete without damage to existing RC (reinforced concrete. Among deteriorating agents, chloride ion is considered as one of the most critical threats due to rapid penetration and direct effect on steel corrosion. In the work, cement mortar samples with 3 w/c (water-to-cement ratios and 4 levels of chloride addition are considered. Conductivity and dielectric constant are measured in the normal frequency range. They increase with strength of mortar and more chloride ions due to denser pore formation. Furthermore, the behaviors of measured EM property are investigated with carbonation velocity and strength, which shows an attempt of application to durability evaluation through EM measurement.

  15. Sugar-metal ion interactions: the complicated coordination structures of cesium ion with D-ribose and myo-inositol.

    Science.gov (United States)

    Hu, Haijian; Xue, Junhui; Wen, Xiaodong; Li, Weihong; Zhang, Chao; Yang, Limin; Xu, Yizhuang; Zhao, Guozhong; Bu, Xiaoxia; Liu, Kexin; Chen, Jia'er; Wu, Jinguang

    2013-11-18

    The novel cesium chloride-D-ribose complex (CsCl·C5H10O5; Cs-R) and cesium chloride-myo-inositol complex (CsCl·C6H12O6; Cs-I) have been synthesized and characterized using X-ray diffraction and FTIR, FIR, THz, and Raman spectroscopy. Cs(+) is eight-coordinated to three chloride ions, O1 and O2 from one D-ribose molecule, O1 from another D-ribose molecule, and O4 and O5 from the third D-ribose molecule in Cs-R. For one D-ribose molecule, the oxygen atom O1 in the ring is coordinated to two cesium ions as an oxygen bridge, O2 is cocoordinated with O1 to one of the two cesium ions, and O4 and O5 are coordinated to the third cesium ion, respectively. O3 does not coordinate to metal ions and only takes part in forming hydrogen bonds. One chloride ion is connected to three cesium ions. Thus, a complicated structure of Cs-D-ribose forms. For Cs-I, Cs(+) is 10-coordinated to three chloride ions, O1 and O2 from one myo-inositol molecule, O3 and O4 from another myo-inositol molecule, O5 and O6 from the third myo-inositol molecule, and O6 from the fourth myo-inositol molecule. One metal ion is connected to four ligands, and one myo-inositol is coordinated to four Cs(+) ions, which is also a complicated coordination structure. Crystal structure results, FTIR, FIR, THz, and Raman spectra provide detailed information on the structure and coordination of hydroxyl groups to metal ions in the cesium chloride-D-ribose and cesium chloride-myo-inositol complexes.

  16. Interactions Between Metal Ions and Carbohydrates: Coordination Behavior of D-Ribose to Lanthanide Ions

    Institute of Scientific and Technical Information of China (English)

    苏允兰; 杨丽敏; 翁诗甫; 吴瑾光

    2002-01-01

    Lanthanum chloride α-D-ribopyranose pentahydrate complex was prepared and speculated its structure from the similar IR spectra of corresponding praseodymium and neodymium-D-ribose complexes, which reveal the coordination behavior of D-ribose to lanthanide ions and give us a model of the interactions between metal ions and carbohydrates.

  17. Hydrolysis of cupric chloride in aqueous ammoniacal ammonium chloride solutions

    Directory of Open Access Journals (Sweden)

    Limpo, J. L.

    1995-06-01

    Full Text Available Cupric solubility in the CuCl2-NH4Cl-NH3-H2O system for chloride concentrations lower than 4 molal in the temperature range 25-60 °C was studied. The experimental results show that for chloride concentration between 3.0 and 1.0 molal the cupric solubility is determined by the solubility of the cupric hydroxychloride Cu(OH1.5Cl0.5. For a chloride concentration value of 4.0 molal, there are two cupric compounds, the hydroxychloride Cu(OH1.5Cl0.5 or the diammine chloride Cu(NH32Cl2, on which the solubility of Cu(II depends, according to the temperature and the value of the ratio [NH3]Total/[Cu]Total.

    Se estudia la solubilidad del Cu(II en el sistema CuCl2-NH4Cl-NH3-H2O para concentraciones de cloruro inferiores a 4 molal en el intervalo de temperaturas 25-60 °C. Los resultados experimentales muestran que, para concentraciones de cloruros comprendidas entre 3,0 y 1,0 molal, la solubilidad cúprica viene determinada por la solubilidad del hidroxicloruro cúprico, Cu(OH1.5Cl0.5. Para concentraciones de cloruro 4,0 molal, existen dos compuestos cúpricos, el hidroxicloruro, Cu(OH1.5Cl0.5 o el cloruro de diamina, Cu(NH32Cl2, de los que, de acuerdo con la temperatura y con el valor de la relación [NH3]Total/[Cu]Total depende la solubilidad del Cu(II.

  18. Ion channels in inflammation.

    Science.gov (United States)

    Eisenhut, Michael; Wallace, Helen

    2011-04-01

    Most physical illness in vertebrates involves inflammation. Inflammation causes disease by fluid shifts across cell membranes and cell layers, changes in muscle function and generation of pain. These disease processes can be explained by changes in numbers or function of ion channels. Changes in ion channels have been detected in diarrhoeal illnesses, pyelonephritis, allergy, acute lung injury and systemic inflammatory response syndromes involving septic shock. The key role played by changes in ion transport is directly evident in inflammation-induced pain. Expression or function of all major categories of ion channels like sodium, chloride, calcium, potassium, transient receptor potential, purinergic receptor and acid-sensing ion channels can be influenced by cyto- and chemokines, prostaglandins, leukotrienes, histamine, ATP, reactive oxygen species and protons released in inflammation. Key pathways in this interaction are cyclic nucleotide, phosphoinositide and mitogen-activated protein kinase-mediated signalling, direct modification by reactive oxygen species like nitric oxide, ATP or protons and disruption of the cytoskeleton. Therapeutic interventions to modulate the adverse and overlapping effects of the numerous different inflammatory mediators on each ion transport system need to target adversely affected ion transport systems directly and locally.

  19. Corrosion Inhibition of Carbon Steel in Chloride and Sulfate Solutions

    Directory of Open Access Journals (Sweden)

    Amr Ahmed Elsayed

    2016-02-01

    Full Text Available Corrosion is a major problem in industry and in infrastructure; a huge sum of expenditure every year is spent on preventing, retarding, and repairing its damages. This work studies the engineering of an inhibitor for carbon steel metal used in the cooling systems containing high concentration of chloride and sulfate ions. For this purpose, the synergy between the dichromate, molybdate and nitrite inhibitors is examined and optimized to the best results. Moreover, care was taken that the proposed inhibitor is compliant with the environmental laws and regulations.

  20. Exhaustividad de la notificación de los casos de sida en Cataluña: un estudio basado en las solicitudes de determinaciones de linfocitos CD4 y en la prescripción de antirretrovirales

    Directory of Open Access Journals (Sweden)

    García de Olalla Rizo Patricia

    1998-01-01

    Full Text Available FUNDAMENTO: Determinar la tasa de notificación de SIDA en Cataluña. MÉTODO: Se utilizan como fuentes de contraste las solicitudes de las determinaciones de linfocitos T CD4+ y la prescripción de antirretrovirales en siete hospitales universitarios de Cataluña entre el 1 de enero y el 31 de junio de 1994. Se consideró que un caso no estaba declarado cuando en la historia clínica existía un diagnóstico de sida (según la definición de Europa 93 y dicho caso no se encontraba incluido en el registro de sida de Cataluña. RESULTADOS: De los 1.370 casos analizados, se detectaron 50 casos de sida no declarados. La tasa de notificación global fue del 98,6%, con un intervalo de confianza del 95% (IC del 95%:98,2-99,0. La mayoría de los casos no declarados eran hombres (72% con una edad media de 37,3 años (DS:11,8, el 52% eran usuarios de drogas por vía parenteral (UDVP, siendo la tuberculosis extrapulmonar la enfermedad diagnóstica más frecuente (16%, el 81,4% presentaban un nivel de linfocitos T CD4+ menor o igual a 200 células /mm3. El 92% de estos casos se detectaron a partir de los registros de determinaciones de linfocitos T CD4+. CONCLUSIONES: La exhaustividad detectada se considera adecuada. Se recomienda usar los registros de determinaciones linfocitarias para este tipo de estudios.

  1. Ecuaciones para eliminar la interferencia de sueros hemolisados, ictéricos e hiperglucémicos en las determinaciones rutinarias de química clínica

    OpenAIRE

    Martha A. Sánchez Rodríguez; Rosa Colunga Reyes; Ma. del Pilar Cedillo Martínez

    2002-01-01

    Introducción: Las muestras hemolisadas, ictéricas o hiperglucémicas, pueden modificar cuantitativamente los resultados de una medición analítica por interferencia, ya que los métodos utilizados para las determinaciones en química clínica están basados en técnicas espectrofotométricas. Objetivo: Cuantificar la interferencia in vitro producida por la presencia en el suero de glucosa, bilirrubina y hemoglobina, a diferentes concentraciones, en las técnicas de urea, creatinina, ácido úrico y cole...

  2. Oxomemazine hydro­chloride

    Science.gov (United States)

    Siddegowda, M. S.; Butcher, Ray J.; Akkurt, Mehmet; Yathirajan, H. S.; Ramesh, A. R.

    2011-01-01

    In the title compound [systematic name: 3-(5,5-dioxo­phen­othia­zin-10-yl)-N,N,2-trimethyl­propanaminium chloride], C18H23N2O2S+·Cl−, the dihedral angle between the two outer aromatic rings of the phenothia­zine unit is 30.5 (2)°. In the crystal, the components are linked by N—H⋯Cl and C—H⋯Cl hydrogen bonds and C—H⋯π inter­actions. PMID:22090928

  3. Simple chloride sensors for continuous groundwater monitoring

    DEFF Research Database (Denmark)

    Thorn, Paul; Mortensen, John

    2012-01-01

    The development of chloride sensors which can be used for continuous, on-line monitoring of groundwater could be very valuable in the management of our coastal water resources. However, sensor stability, drift, and durability all need to be addressed in order for the sensors to be used...... in continuous application. This study looks at the development of a simple, inexpensive chloride electrode, and evaluates its performance under continuous use, both in the laboratory and in a field test in a monitoring well. The results from the study showed a consistent response to changing chloride...... sensor remained responsive even at low chloride concentrations, where the conductivity electrode was no longer responding to changing chloride levels. With the results, it is believed that the simple chloride sensor could be used for continuous monitoring of groundwater quality....

  4. Chloride ingress in cement paste and mortar

    Energy Technology Data Exchange (ETDEWEB)

    Jensen, O.M.; Hansen, P.F.; Coats, A.M.; Glasser, F.P.

    1999-09-01

    In this paper chloride ingress in cement paste and mortar is followed by electron probe microanalysis. The influence of several paste and exposure parameters on chloride ingress are examined (e.g., water-cement ratio, silica fume addition, exposure time, and temperature). The measurements are modelled on Fick's law modified by a term for chloride binding. Inclusion of chloride binding significantly improves the profile shape of the modelled ingress profiles. The presence of fine aggregate and formation of interfacial transition zones at paste-aggregate boundaries does not significantly affect diffusion rates.

  5. Time-space consistent collocation method of RBF for chloride ion heterogeneous diffusion problem in concrete%混凝土中氯离子非均质扩散问题时空一致径向基函数配点法

    Institute of Scientific and Technical Information of China (English)

    张芹; 郭力; 张秉超

    2012-01-01

    针对混凝土中氯离子扩散过程中扩散系数的非均质性导致的非线性问题,采用区域分解法并融入无网格法中的径向基函数求解思想,建立了时空一致径向基函数配点法.该方法将时间和空间区域同时分解,在相应子域上对未知函数进行径向基函数展开.针对含有Neumann边界条件的非均质扩散问题建立了Hermite型近似函数配点求解方法.该方法避免了对时间域采用差分法求解引起的迭代求解困难,对求解非均质扩散系数的问题求解具有一定优势.用Matlab语言编制了相应的求解程序,通过2个非均质扩散问题算例,验证了所提方法的正确性和有效性.所提方法为研究复杂环境下混凝土结构的耐久性问题提供了一种新的数值方法.%According to the nonlinear problem caused by heterogeneous diffusivity in the diffusion process of chloride ion in concrete, a time-space consistent collocation method is developed with the domain decomposition method and the methodology of the radial basis function (RBF) in the mesh-less method. Unknown arguments are expanded via RBFs in the corresponding sub-domain with simultaneous decomposing of the time and space domain. Additionally, a Hermite collocation method of the RBF is constructed to solve the heterogeneous diffusion problem with Neumann boundary conditions. Compared with the finite difference process on solving time domain issues, the proposed method reduces the difficulty of iterative procedure and results in a more easy application to heterogeneous diffusion problems. The Matlab program of the developed method is subsequently implemented. Two numerical examples are performed to evaluate the accuracy and efficiency of the developed model. The examples clearly demonstrate that the developed method has more distinguished advantages than the finite element method in analyzing heterogeneous diffusion problems. The proposed method provides new guidelines for the

  6. ENVIRONMENTAL EXPOSURE TO VINYL CHLORIDE

    Directory of Open Access Journals (Sweden)

    Henryka Langauer-Lewowicka

    2010-09-01

    Full Text Available Vinyl chloride (VC monomer is a wellknown carcinogenic and mutagenic substance causes liver damages, angiosarcoma of the liver, acro – osteolysis, sclerodermalike changes in workers chronically exposed to this gas. There are following VC emitors to the environment: VC production plants, polymerization facilities and planes where polyvinyl products are fabricated. Because of that, the general population is coming into VC contact through polluted air, food and water. VC concentration in all mentioned sites is very low, often not detectable. There was found any health risk for the general population. The VC air concentration in the vicinity to antropogenic emitors is always higher. Such a situation may causes undesirable health effect for residents living in the neighbourhood. Epidemiological studies are performed to detect the adverse VC effect in selected cohorts. Non of the study did not confirmed cases of angiosarcoma among residents living near a vinyl chloride sites. VC production is growing permanently, so VC emission will be higher. Because of that health monitoring of general population and especially of selected groups seems to be necessary in the future.

  7. Influence of flexural fatigue on chloride threshold value for the corrosion of steels in Ca(OH){sub 2} solutions

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Linhua, E-mail: hhulhjiang@gmail.com [College of Mechanics and Materials, Hohai University, 1 Xikang Rd., Nanjing, 210098 (China); Hydraulic Engineering Research Center for New Materials and Protection, Jiangsu Province, 1 Xikang Rd., Nanjing, 210098 (China); Liu, Hao; Wang, Yongliang; Zhang, Yan; Song, Zijian; Xu, Jinxia; Jin, Ming; Jiang, Peng; Xu, Yi; Gao, Hailang [College of Mechanics and Materials, Hohai University, 1 Xikang Rd., Nanjing, 210098 (China)

    2015-08-15

    The flexural fatigue was enforced on reinforced concrete beam with stress level of 0.6 and different fatigue life cycles. Steels removed from the beams were soaked in the saturated Ca(OH){sub 2} solution, which was used as a simulated concrete pore solution. The NaCl solution was chosen as the source of chloride ions. The Chloride Threshold Values (CTV) were detected by combining the open-circuit potentials (E{sub corr}) with the corrosion current densities (i{sub corr}), which were obtained by electrochemical impedance spectroscopy (EIS). The changes of microstructure caused by the flexural fatigue were observed by scanning electron microscopy (SEM). The results showed that as the fatigue cycle times increased, the CTV decreased under a certain stress level and range of fatigue life cycles. The grains became finer and cracks appeared on the surface of the steels. While the capacitive arcs under no flexural fatigue decreased gradually with the addition of chloride ions, the ones under flexural fatigue presented no regularity. Cracks at the surface were expanded because of sustaining flexural fatigue, which degenerated the later resistance to chloride ions of the steels. - Highlights: • The influence of flexural fatigue on chloride threshold value was examined. • The chloride threshold values vary with different fatigue life cycles. • The corrosion behavior depends on the surface integrity of the steels.

  8. Chloride ingress in concrete as measured by field exposure tests in the atmospheric, tidal and submerged zones of a tropical marine environment

    Energy Technology Data Exchange (ETDEWEB)

    Roy, S.K. (National Univ. of Singapore (Singapore). School of Building and Estate Management); Chye, Liam Kok (Matcor Technology and Services (Singapore)); Northwood, D.O. (National Univ. of Singapore (Singapore). Dept. of Mechanical and Production Engineering Univ. of Windsor, Ontario (Canada). Engineering Materials Group)

    1993-11-01

    Five grades of concrete were exposed in the atmosphere, tidal and submerged zones of a tropical marine environment for times up to 80 weeks and the chloride ion ingress profiles determined. The measured chloride profiles were compared with profiles calculated on the basis of diffusion theory and the agreement was found to be reasonably good for all 3 zones. Diffusion coefficients, D, for the chloride ion calculated from the measured ingress profiles agreed well with previous data from laboratory tests and from surveys of marine structures. D was found to be mainly dependent on the water/cement (W/C) ratio and changed little with the addition of superplasticizers. The use of data for the diffusion coefficient, D, and equilibrium surface chloride level, Ce, obtained from the chloride ingress profiles, to the calculation of the time-to-initiation for corrosion of the steel reinforcement is briefly discussed.

  9. Rapid chloride permeability test for durability study of carbon nanoreinforced mortar

    Science.gov (United States)

    Alafogianni, P.; Dalla, P. T.; Tragazikis, I. K.; Barkoula, N.-M.; Matikas, T. E.

    2015-03-01

    The addition of a conductive admixture in a cement-based material could lead to innovative products with multifunctional features. These materials are designed to possess enhanced properties, such as improved mechanical properties, electrical and thermal conductivity, and piezo-electric characteristics. Carbon nanotubes (CNTs) can be used as nano-reinforcement in cement-based materials because of their huge aspect ratio as well as their extremely large specific surface area. For cement-based composites, one of the major types of environmental attack is the chloride ingress, which leads to corrosion of the material and, subsequently, to the reduction of strength and serviceability of the structure. A common method of preventing such deterioration is to avert chlorides from penetrating the structure. The penetration of the concrete by chloride ions is a slow process. It cannot be determined directly in a time frame that would be useful as a quality control measure. Therefore, in order to assess chloride penetration, a test method that accelerates the process is needed, to allow the determination of diffusion values in a reasonable time. In the present research, nanomodified mortars with various concentrations of multi-wall carbon nanotubes (0.2% wt. cement CNTs - 0.6% wt. cement CNTs) were used. The chloride penetration in these materials was monitored according to ASTM C1202 standard. This is known as the Coulomb test or Rapid Chloride Permeability Test (RCPT).

  10. Determination of persimmon leaf chloride contents using near-infrared spectroscopy (NIRS).

    Science.gov (United States)

    de Paz, José Miguel; Visconti, Fernando; Chiaravalle, Mara; Quiñones, Ana

    2016-05-01

    Early diagnosis of specific chloride toxicity in persimmon trees requires the reliable and fast determination of the leaf chloride content, which is usually performed by means of a cumbersome, expensive and time-consuming wet analysis. A methodology has been developed in this study as an alternative to determine chloride in persimmon leaves using near-infrared spectroscopy (NIRS) in combination with multivariate calibration techniques. Based on a training dataset of 134 samples, a predictive model was developed from their NIR spectral data. For modelling, the partial least squares regression (PLSR) method was used. The best model was obtained with the first derivative of the apparent absorbance and using just 10 latent components. In the subsequent external validation carried out with 35 external data this model reached r(2) = 0.93, RMSE = 0.16% and RPD = 3.6, with standard error of 0.026% and bias of -0.05%. From these results, the model based on NIR spectral readings can be used for speeding up the laboratory determination of chloride in persimmon leaves with only a modest loss of precision. The intermolecular interaction between chloride ions and the peptide bonds in leaf proteins through hydrogen bonding, i.e. N-H···Cl, explains the ability for chloride determinations on the basis of NIR spectra.

  11. Modelling chloride diffusion in concrete: Effect of fly ash and slag

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, M.D.A. [Univ. of Toronto, Ontario (Canada). Dept. of Civil Engineering; Bamforth, P.B. [Taywood Engineering Ltd., Southall (United Kingdom)

    1999-04-01

    The ability of concrete to resist the penetration of chloride ions is a critical parameter in determining the service life of steel-reinforced concrete structures exposed to deicing salts or marine environments. Data from long-term field and laboratory studies of concrete exposed to chloride environments were analyzed using a chloride transport model developed at the University of Toronto. The results show that the incorporation of fly ash and slag may have little impact on transport properties determined at early ages (e.g., 28 days), but can lead to order of magnitude improvements in the long term. This means that the rate of chloride penetration during the first 6 months or so of exposure is similar for concretes with and without these materials. However, after a few years of exposure, chloride ingress slows to a much-decreased rate in fly ash and slag concretes, leading to dramatic increases in the predicted service life. Predictive models and laboratory test methods for determining chloride ingress should take account of the time-dependent nature of the transport processes in concrete, especially when supplementary cementing materials, such as fly ash or slag, are used.

  12. Comparing polyaluminum chloride and ferric chloride for antimony removal.

    Science.gov (United States)

    Kang, Meea; Kamei, Tasuku; Magara, Yasumoto

    2003-10-01

    Antimony has been one of the contaminants required to be regulated, however, only limited information has been collected to date regarding antimony removal by polyaluminium chloride (PACl) and ferric chloride (FC). Accordingly, the possible use of coagulation by PACl or FC for antimony removal was investigated. Jar tests were used to determine the effects of solution pH, coagulant dosage, and pre-chlorination on the removal of various antimony species. Although high-efficiency antimony removal by aluminum coagulation has been expected because antimony is similar to arsenic in that both antimony and arsenic are a kind of metalloid in group V of the periodic chart, this study indicated: (1) removal density (arsenic or antimony removed per mg coagulant) for antimony by PACl was about one forty-fifth as low as observed for As(V); (2) although the removal of both Sb(III) and Sb(V) by coagulation with FC was much higher than that of PACl, a high coagulant dose of 10.5mg of FeL(-1) at optimal pH of 5.0 was still not sufficient to meet the standard antimony level of 2 microg as SbL(-1) for drinking water when around 6 microg as SbL(-1) were initially present. Consequently, investigation of a more appropriate treatment process is necessary to develop economical Sb reduction; (3) although previous studies concluded that As(V) is more effectively removed than As(III), this study showed that the removal of Sb(III) by coagulation with FC was much more pronounced than that of Sb(V); (4) oxidation of Sb(III) with chlorine decreased the ability of FC to remove antimony. Accordingly, natural water containing Sb(III) under anoxic condition should be coagulated without pre-oxidation.

  13. Determination of {sup 60}Co sorption in natural clinoptilolite; Determinacion de la sorcion de {sup 60}Co en clinoptilolita natural

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez B, E.; Granados C, F. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

    1997-07-01

    It was studied the clinoptilolite behavior coming from a deposit in Taxco, Guerrero in hydration and stabilization conditions with sodium for determining its sorption properties. The ion exchange process was carried out through gamma spectrometry using a CoCl{sub 2} solution marked with {sup 60} Co at p H 6.5 in different contact times. It was observed a maximum sorption of 0.408 m eq Co{sup +2}/g mineral, from 0.314 m eq Co{sup +2}/g mineral correspond at ion exchange. (Author)

  14. Electrochemical Behavior of Copper in Thionyl Chloride Solutions.

    Science.gov (United States)

    1980-12-01

    lithium - thionyl chloride batteries . Thionyl chloride is known *3 to react...electrolyte for lithium - thionyl chloride batteries . 8R. K. McAlpine and B. A. Soule, Prescott and Johnson’s Qualitative Chemical Analysis, D. Van...black carbon electrodes, cupric chloride appears to be a useful cathode additive for lithium - thionyl chloride batteries . Preliminary results2l

  15. Corrosion behaviour of a stream generator tube material in simulated steam generator feedwater containing chlorides and sulphates

    Energy Technology Data Exchange (ETDEWEB)

    Bojinov, M.; Kinnunen, P.; Laitinen, T.; Maekelae, K.; Saario, T.; Sirkiae, P.; Yliniemi, K. [VTT Manufacturing Technology, Espoo (Finland); Buddas, T.; Halin, M.; Tompuri, K. [Fortum Power and Heat Oy, Loviisa Power Plant (Finland)

    2002-07-01

    The goal of the present work has been to assess the effect of relatively high concentrations of anionic impurities (Cl{sup -}, SO{sub 4}{sup 2-}) on the corrosion behaviour of Ti-stabilised stainless steel SG tubes in simulated steam generator feed-water. The main observations of this work can be summarised as follows: Sulphate ions seem to be more aggressive than chloride ions towards the primary passive film on 08X18H10T stainless steel. The results may indicate that it is more important to have a low concentration of sulphate ions than of chloride ions in secondary side water when the effects of chemical conditions on tube degradation are considered. The presence of chloride ions seems to weaken the detrimental effect of sulphate ions on the stability of oxide films growing on 08X18H10T stainless steel. No localised corrosion features of 08X18H10T stainless steel were detected in the voltammetric and impedance measurements in solutions containing up to 5000 ppb sulphates, chlorides or both of the anions. (authors)

  16. Chloride adsorption by calcined layered double hydroxides in hardened Portland cement paste

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Seyoon [School of Engineering, Kings College, University of Aberdeen, Aberdeen AB24 3UE (United Kingdom); Moon, Juhyuk, E-mail: juhyuk.moon@stonybrook.edu [Civil Engineering Program, Department of Mechanical Engineering, State University of New York at Stony Brook, New York 11794 (United States); Bae, Sungchul [Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720 (United States); Duan, Xiaonan [Department of Materials Science and Engineering, Cornell University, Ithaca, NY 14853 (United States); Giannelis, Emmanuel P. [Department of Materials Science and Engineering, Cornell University, Ithaca, NY 14853 (United States); Center for Refining and Petrochemicals, The Research Institute, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Monteiro, Paulo M. [Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720 (United States)

    2014-06-01

    This study investigated the feasibility of using calcined layered double hydroxides (CLDHs) to prevent chloride-induced deterioration in reinforced concrete. CLDHs not only adsorbed chloride ions in aqueous solution with a memory effect but also had a much higher binding capacity than the original layered double hydroxides (LDHs) in the cement matrix. We investigated this adsorption in hardened cement paste in batch cultures to determine adsorption isotherms. The measured and theoretical binding capacities (153 mg g{sup −1} and 257 mg g{sup −1}, respectively) of the CLDHs were comparable to the theoretical capacity of Friedel's salt (2 mol mol{sup −1} or 121 mg g{sup −1}), which belongs to the LDH family among cementitious phases. We simulated chloride adsorption by CLDHs through the cement matrix using the Fickian model and compared the simulation result to the X-ray fluorescence (XRF) chlorine map. Based on our results, it is proposed that the adsorption process is governed by the chloride transport through the cement matrix; this process differs from that in an aqueous solution. X-ray diffraction (XRD) analysis showed that the CLDH rebuilds the layered structure in a cementitious environment, thereby demonstrating the feasibility of applying CLDHs to the cement and concrete industries. - Highlights: • We examine the adsorption equilibrium and kinetics of CLDH in the hydrated cement. • CLDH capacity to bind chloride ions in the hydrated cement paste is determined. • We model chloride adsorption by CLDH through the cement matrix. • CLDH reforms the layered structure with ion adsorption in the cement matrix.

  17. Uranium potentiometer determination in inactive atmosphere with ferric sulfate; Determinacion poteniometrica de uranio en atmosfera inerte con sulfato ferrico

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez Cellini, R.; Alonso Lopez, J.

    1956-07-01

    Potentiometric titration of Uranium with (SO{sub 4}){sub 3} Fe{sub 2}, using Cd as reducing agent has been studied; acidity and sensibility of this reaction are fixed. This method yields good results for uranite group, removing previously phosphate by ion exchange with Amberlite IR-120. (Author)

  18. Sodium chloride precipitation reaction coefficient from crystallization experiment in a microfluidic device

    Science.gov (United States)

    Naillon, A.; Joseph, P.; Prat, M.

    2017-04-01

    The crystal growth of sodium chloride from an aqueous solution is studied from evaporation experiments in microfluidic channels in conjunction with analytical and numerical computations. The crystal growth kinetics is recorded using a high speed camera in order to determine the intrinsic precipitation reaction coefficient. The study reveals that the crystal growth rates determined in previous studies are all affected by the ions transport phenomena in the solution and thus not representative of the precipitation reaction. It is suggested that accurate estimate of sodium chloride precipitation reaction coefficient presented here offers new opportunities for a better understanding of important issues involved in the damages of porous materials induced by the salt crystallization.

  19. Nucleophilic Substitution and Redox Reactions with alpha-Chloro beta-Oxo Sulfenyl Chlorides

    DEFF Research Database (Denmark)

    El-Essawy, Farag A.G.; Yassin, Salah M.; El-Sakka, Ibrahim A.

    1998-01-01

    Alpha-Chloro sulfenyl chlorides such as 1 and 4 could not be reduced to the corresponding disulfides. Under reducing conditions they are instead dechlorinated to the corresponding thiocarbonyl compounds. Starting from the chroman-4-one derivatives 1 a number of 1,3,4-oxadithiins 3 have been...... prepared. Sulfenyl chlorides 1 and 4 have been derivatized with p-toluenesulfinate, methoxide, and cyanide ions as well as with primary and secondary amines, with thiophenol and with thiobenzoic acid. The molecular structure of thiocyanate 8a has been determined by X-ray crystallography....

  20. Dengue virus M protein C-terminal peptide (DVM-C) forms ion channels.

    Science.gov (United States)

    Premkumar, A; Horan, C R; Gage, P W

    2005-03-01

    A chemically synthesized peptide consisting of the C-terminus of the M protein of the Dengue virus type 1 strain Singapore S275/90 (DVM-C) produced ion channel activity in artificial lipid bilayers. The channels had a variable conductance and were more permeable to sodium and potassium ions than to chloride ions and more permeable to chloride ions than to calcium ions. Hexamethylene amiloride (100 microM) and amantadine (10 microM), blocked channels formed by DVM-C. Ion channels may play an important role in the life cycle of many viruses and drugs that block these channels may prove to be useful antiviral agents.

  1. 29 CFR 1915.1017 - Vinyl chloride.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 7 2010-07-01 2010-07-01 false Vinyl chloride. 1915.1017 Section 1915.1017 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR... § 1915.1017 Vinyl chloride. Note: The requirements applicable to shipyard employment under this...

  2. 29 CFR 1926.1117 - Vinyl chloride.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 8 2010-07-01 2010-07-01 false Vinyl chloride. 1926.1117 Section 1926.1117 Labor... (CONTINUED) SAFETY AND HEALTH REGULATIONS FOR CONSTRUCTION Toxic and Hazardous Substances § 1926.1117 Vinyl chloride. Note: The requirements applicable to construction work under this section are identical to...

  3. Chemische contaminanten in diervoeder additief Choline Chloride

    NARCIS (Netherlands)

    Traag, W.A.; Hoogenboom, L.A.P.; Jong, de J.; Egmond, van H.J.; Dam, ten G.

    2010-01-01

    Dit briefrapport beschrijft de resultaten van een onderzoek naar chemische contaminanten in Choline Chloride. De doelstellingen waren: 1) Inzicht te verkrijgen in het voorkomen van (gebromeerde) vlamvertragers en broomdioxines in het diervoederadditief Choline Chloride en het, op basis van de result

  4. Chloride ingress in cement paste and mortar

    DEFF Research Database (Denmark)

    Jensen, Ole Mejlhede; Hansen, Per Freiesleben; Coats, Alison M.

    1999-01-01

    In this paper chloride ingress in cement paste and mortar is followed by electron probe microanalysis. The influence of several paste and exposure parameters on chloride ingress are examined (e.g., water-cement ratio, silica fume addition, exposure time, and temperature), The measurements...

  5. Metallocene electrochemistry. 2. Reduction-oxidation behavior of nickelocene in the room-temperature alkylpyridinium chloride-aluminum chloride melt system

    Energy Technology Data Exchange (ETDEWEB)

    Gale, R.J.; Job, R.

    1981-01-01

    In neutral 1:1 molar ratio mixtures of AlCl/sub 3/-1-butylpyridinium chloride, at 40/sup 0/C, nickelocene undergoes a reversible 1-electron charge-transfer reaction, with E/sub 1/2/ = -0.165 V vs. Al (2:1) reference. Evidence is presented to show that both nickelocene and the nickelocenium (III) ion are unstable in chloride ion rich solvents. Spontaneous oxidation to the nickelocenium cation occurs in acidic (> 1:1) melts, and a stable dication is formed reversibly at E/sub 1/2/ = +0.912 V vs. Al (2:1) reference. Electronic spectra of nickelocene species in the II, III, and IV oxidation states have been recorded in these melts. The spectrum of the dication species contains bands at 412, 438, 532 nm.

  6. Chloride Transport in Undersea Concrete Tunnel

    Directory of Open Access Journals (Sweden)

    Yuanzhu Zhang

    2016-01-01

    Full Text Available Based on water penetration in unsaturated concrete of underwater tunnel, a diffusion-advection theoretical model of chloride in undersea concrete tunnel was proposed. The basic parameters including porosity, saturated hydraulic conductivity, chloride diffusion coefficient, initial water saturation, and moisture retention function of concrete specimens with two water-binder ratios were determined through lab-scale experiments. The variation of chloride concentration with pressuring time, location, solution concentration, initial saturation, hydraulic pressure, and water-binder ratio was investigated through chloride transport tests under external water pressure. In addition, the change and distribution of chloride concentration of isothermal horizontal flow were numerically analyzed using TOUGH2 software. The results show that chloride transport in unsaturated concrete under external water pressure is a combined effect of diffusion and advection instead of diffusion. Chloride concentration increased with increasing solution concentration for diffusion and increased with an increase in water pressure and a decrease in initial saturation for advection. The dominant driving force converted with time and saturation. When predicting the service life of undersea concrete tunnel, it is suggested that advection is taken into consideration; otherwise the durability tends to be unsafe.

  7. Synthesis and characterization of zinc chloride containing poly(acrylic acid) hydrogel by gamma irradiation

    Science.gov (United States)

    Park, Jong-Seok; Kuang, Jia; Gwon, Hui-Jeong; Lim, Youn-Mook; Jeong, Sung-In; Shin, Young-Min; Seob Khil, Myung; Nho, Young-Chang

    2013-07-01

    In this study, the characterization of zinc chloride incorporated into a poly(acrylic acid) (PAAc) hydrogel prepared by gamma-ray irradiation was investigated. Zinc chloride powder with different concentrations was dissolved in the PAAc solution, and it was crosslinked with gamma-ray irradiation. The effects of various parameters such as zinc ion concentration and irradiation doses on characteristics of the hydrogel formed were investigated in detail for obtaining an antibacterial wound dressing. In addition, the gel content, pH-sensitive (pH 4 or 7) swelling ratio, and UV-vis absorption spectra of the zinc particles in the hydrogels were characterized. Moreover, antibacterial properties of these new materials against Staphylococcus aureus and Escherichia coli strains were observed on solid growth media. The antibacterial tests indicated that the zinc chloride containing PAAc hydrogels have good antibacterial activity.

  8. Synthesis of Macrocyclic Ionophore for the Development of Highly Selective Chloride Sensor

    Directory of Open Access Journals (Sweden)

    Sameena Mehtab

    2015-03-01

    Full Text Available The macrocyclic ligands 3,8,12,17-tetramethyl-2,18,9,11-bipyridyl-1,4,7,10,13,16-hexaazacyclooctadecanetetrahydro bromide has been synthesized and explored as suitable ionophores for chloride selective membrane sensors. It displays Nernstian behavior (59.2 mV decade-1 across the range of 4.1 × 10-8 to 1.0 × 10-2 M. The detection limit of the electrode is ~ 15 nM and the response time and life times are 14 s and eight weeks respectively over a wide pH range (3.5 - 9.5. Interference from other anions is very low and it can be used as indicator electrode in the potentiometric titration of chloride ions and to determine chloride in agricultural soil water samples.

  9. Methods for evaluating potential sources of chloride in surface waters and groundwaters of the conterminous United States

    Science.gov (United States)

    Granato, Gregory E.; DeSimone, Leslie A.; Barbaro, Jeffrey R.; Jeznach, Lillian C.

    2015-09-04

    Chloride exists as a major ion in most natural waters, but many anthropogenic sources are increasing concentrations of chloride in many receiving waters. Although natural concentrations in continental waters can be as high as 200,000 milligrams per liter, chloride concentrations that are suitable for freshwater ecology, human consumption, and agricultural and industrial water uses commonly are on the order of 10 to 1,000 milligrams per liter. “Road salt” frequently is identified as the sole source of anthropogenic chloride, but only about 30 percent of the salt consumed and released to the environment is used for deicing. Furthermore, several studies in Southern States where the use of deicing salt is minimal also show anthropogenic chloride in rising concentrations and in strong correlation to imperviousness and road density. This is because imperviousness and road density also are strongly correlated to population density. The term “road salt” is a misnomer because deicers applied to parking lots, sidewalks, and driveways can be a substantial source of chloride in some catchments because these land covers are comparable to roadways as a percentage of the total impervious area and commonly receive higher salt application rates than some roadways. Other sources of anthropogenic chloride include wastewater, dust control on unpaved roads, fertilizer, animal waste, irrigation, aquaculture, energy production wastes, and landfill leachates. The assumption that rising chloride concentrations in surface water or groundwater is indicative of contamination by deicing chemicals rather than one or more other potential sources may preclude the identification of toxic, carcinogenic, mutagenic, or endocrine-disrupting contaminants that are associated with many sources of elevated chloride concentrations. Once the sources of anthropogenic chloride in an area of interest have been identified and measured, water and solute budgets can be estimated to guide decisionmakers to

  10. Determination of Water Soluble Fluoride, Chloride, Bromide and Nitrate in Iron Ores by Supersonic Extraction-Ion Chromatography%超声提取-离子色谱法测定铁矿石中水溶性氟氯溴及硝酸根

    Institute of Scientific and Technical Information of China (English)

    胡德新; 马德起; 安鹏升; 王振坤; 王虹; 李权斌; 谷松海; 魏红兵

    2012-01-01

    An ion chromatography method with ultrasonic extraction has been developed to simultaneously determine the water solubility of fluoride, chloride, bromide and nitrate in iron ores. The sample solution was extracted ultrasonically and precipitation separation was carried out by centrifugation. The clarified solution was passed through IC-RP, IC-Na and a 0.22 pjn filter membrane. The anions were separated and data were collected by using AS-19 type anion separation column and ASRS 300-4 mm self-electric chemistry suppressor with the 25.00 mmol/L NaOH as eluent. The organic matter in the sample solution was absorbed by IC-RP column and the heavy metal ions were replaced by IC-Na column, which is the same cation as that in eluent. Based on the study of the extraction efficiency for water solubility anions, the extraction time was 30 min. In order to eliminate the effect of a negative peak from water, a certain amount of eluent was added into the standard and sample solutions to make the conductivity in each solution match each other. Under optimal conditions, the detection limits of F- , Cl- , Br~ and NO3~ were 2.1, 3.5, 2.5 and 2.0 |Xg/g, respectively. The linear correlation was good for the work curve, and the linearly dependent coefficient was greater than 0. 999. The accuracy and precision of this method was verified by iron ore standard material GBW 07218a and the results were consistent with certified values. The RSD (? = 10) was less than 5% and recovery rates with interior standard were 96% - 104%. The results for the actual samples were consistent with those obtained by ion selective electrode method. The method has the benefits of applying to a wide linear range, is simple and has rapid and high efficiency, making it suitable for routine lab inspection work.%铁矿石样品经超声提取、离心机分离沉淀后,分别通过IC-RP柱、IC-Na柱及0.22 μm微孔过滤膜过滤,25.00 mmol/L NaOH溶液作为淋洗液,利用AS-19型阴离子分离柱和ASRS 300

  11. Study on All-Solid-State Chloride Sensor Based on Tin Oxide/Indium Tin Oxide Glass

    Science.gov (United States)

    Cheng, Jui-Fu; Chou, Jung-Chuan; Sun, Tai-Ping; Hsiung, Shen-Kan; Kao, Hui-Ling

    2011-03-01

    An all-solid-state chloride electrode based on a tin oxide (SnO2)/indium tin oxide (ITO) glass was developed in this study. The sensing membrane of the electrode was prepared by mixing poly(vinyl chloride) (PVC), bis(2-ethylhexyl) sebacate (DOS), [4,5-dimethy-l-3,6-bis(dodecyloxy)-1,2-phenylene] bis(mercury chloride) (ETH9033), and tridodecylmethyl ammonium chloride (TDDMACl). The mixed solution was mixed with tetrahydrofuran (THF), and then dropped on the sensing window of SnO2/ITO glass. According to the experimental results, the optimal weight ratio were PVC:DOS:ETH9033:TDDMACl=33:66:2:5. At this optimum weight ratio, the sensitivity was 54 mV/dec while the range of linear concentrations of NaCl solutions was between 10-4 and 1 M. The lower detection limit of the sensor reached 8×10-5 M and the response time was less than 1 s. The selectivity coefficient was consistent with the theory of Hofmeister lipophilicity. The lifetime was over 60 days and the repeatability was over 50 times. Moreover, the chloride ion sensor was successfully applied to detecting chloride ions in rinsing solutions for contact lenses, and the experimental results revealed that the correlation coefficient was 0.99.

  12. The Effect of Silver Chloride Formation on the Kinetics of Silver Dissolution in Chloride Solution

    Science.gov (United States)

    Ha, Hung; Payer, Joe

    2011-01-01

    The precipitation and growth of AgCl on silver in physiological NaCl solution were investigated. AgCl was found to form at bottom of scratches on the surface which may be the less effective sites for diffusion or the favorable sites for heterogeneous nucleation. Patches of silver chloride expanded laterally on the substrate until a continuous film formed. The ionic transport path through this newly formed continuous film was via spaces between AgCl patches. As the film grew, the spaces between AgCl patches closed and ion transport was primarily via micro-channels running through AgCl patches. The decrease of AgCl layer conductivity during film growth were attributed to the clogging of micro-channels or decrease in charge carrier concentration inside the micro-channels. Under thin AgCl layer, i.e. on the order of a micrometer, the dissolution of silver substrate was under mixed activation-Ohmic control. Under thick AgCl layer, i.e. on the order of tens of micrometers, the dissolution of silver substrate was mediated by the Ohmic resistance of AgCl layer. PMID:21516171

  13. The Effect of Silver Chloride Formation on the Kinetics of Silver Dissolution in Chloride Solution.

    Science.gov (United States)

    Ha, Hung; Payer, Joe

    2011-02-28

    The precipitation and growth of AgCl on silver in physiological NaCl solution were investigated. AgCl was found to form at bottom of scratches on the surface which may be the less effective sites for diffusion or the favorable sites for heterogeneous nucleation. Patches of silver chloride expanded laterally on the substrate until a continuous film formed. The ionic transport path through this newly formed continuous film was via spaces between AgCl patches. As the film grew, the spaces between AgCl patches closed and ion transport was primarily via micro-channels running through AgCl patches. The decrease of AgCl layer conductivity during film growth were attributed to the clogging of micro-channels or decrease in charge carrier concentration inside the micro-channels. Under thin AgCl layer, i.e. on the order of a micrometer, the dissolution of silver substrate was under mixed activation-Ohmic control. Under thick AgCl layer, i.e. on the order of tens of micrometers, the dissolution of silver substrate was mediated by the Ohmic resistance of AgCl layer.

  14. Chloride Ingress into Concrete under Water Pressure

    OpenAIRE

    Lund, Mia Schou; Sander, Lotte Braad; Grelk, Bent; Hansen, Kurt Kielsgaard

    2011-01-01

    The chloride ingress into concrete under water pressures of 100 kPa and 800 kPa have been investigated by experiments. The specimens were exposed to a 10% NaCl solution and water mixture. For the concrete having w/c = 0.35 the experimental results show the chloride diffusion coefficient at 800 kPa (~8 atm.) is 12 times greater than at 100 kPa (~1 atm.). For w/c = 0.45 and w/c = 0.55 the chloride diffusion coefficients are 7 and 3 times greater. This means that a change in pressure highly infl...

  15. Reliability-Based Planning of Chloride Measurements

    DEFF Research Database (Denmark)

    Sørensen, John Dalsgaard; Engelund, S.

    1996-01-01

    on measurements of the chloride content obtained from the given structure. In the present paper optimal planning of measurements of the chloride content in reinforced concrete structures is considered. It is shown how optimal experimental plans can be obtained using FORM-analysis. Bayesian statistics are used......In reinforced concrete structures corrosion is initiated when the chloride concentration around the reinforcement exceeds a threshold value. If corrosion starts then expensive repairs can be necessary. The estimation of the probability that corrosion has been initiated in a given structure is based...

  16. Structural foundations of optogenetics: Determinants of channelrhodopsin ion selectivity.

    Science.gov (United States)

    Berndt, Andre; Lee, Soo Yeun; Wietek, Jonas; Ramakrishnan, Charu; Steinberg, Elizabeth E; Rashid, Asim J; Kim, Hoseok; Park, Sungmo; Santoro, Adam; Frankland, Paul W; Iyer, Shrivats M; Pak, Sally; Ährlund-Richter, Sofie; Delp, Scott L; Malenka, Robert C; Josselyn, Sheena A; Carlén, Marie; Hegemann, Peter; Deisseroth, Karl

    2016-01-26

    The structure-guided design of chloride-conducting channelrhodopsins has illuminated mechanisms underlying ion selectivity of this remarkable family of light-activated ion channels. The first generation of chloride-conducting channelrhodopsins, guided in part by development of a structure-informed electrostatic model for pore selectivity, included both the introduction of amino acids with positively charged side chains into the ion conduction pathway and the removal of residues hypothesized to support negatively charged binding sites for cations. Engineered channels indeed became chloride selective, reversing near -65 mV and enabling a new kind of optogenetic inhibition; however, these first-generation chloride-conducting channels displayed small photocurrents and were not tested for optogenetic inhibition of behavior. Here we report the validation and further development of the channelrhodopsin pore model via crystal structure-guided engineering of next-generation light-activated chloride channels (iC++) and a bistable variant (SwiChR++) with net photocurrents increased more than 15-fold under physiological conditions, reversal potential further decreased by another ∼ 15 mV, inhibition of spiking faithfully tracking chloride gradients and intrinsic cell properties, strong expression in vivo, and the initial microbial opsin channel-inhibitor-based control of freely moving behavior. We further show that inhibition by light-gated chloride channels is mediated mainly by shunting effects, which exert optogenetic control much more efficiently than the hyperpolarization induced by light-activated chloride pumps. The design and functional features of these next-generation chloride-conducting channelrhodopsins provide both chronic and acute timescale tools for reversible optogenetic inhibition, confirm fundamental predictions of the ion selectivity model, and further elucidate electrostatic and steric structure-function relationships of the light-gated pore.

  17. Spectrophotometric determination of silica in water with Hach equipment; Determinacion espectrofotometrica de silicio en aguas con equipo Hach

    Energy Technology Data Exchange (ETDEWEB)

    Acosta L, E. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)]. e-mail: eal@nuclear.inin.mx

    1992-06-15

    The method for the determination of the silica element in water, demineralized water, raw waters, laundry waters, waters treated with ion exchange resins and sea waters using the indicated technique in the operation manual of the Hach equipment with a DR/3 spectrophotometer is described. This method covers the determination of the silica element in the interval from 0 to 1.5 mg/l on 50 ml. of base sample. These limits its can be variable if the size of the used aliquot one is changed for the final determination of the silica element. (Author)

  18. Meso-scale modeling of chloride diffusion in concrete with consideration of effects of time and temperature

    Institute of Scientific and Technical Information of China (English)

    Li-cheng WANG; Tamon UEDA

    2009-01-01

    A meso-scale truss network model was developed to predict chloride diffusion in concrete.The model regards concrete as a three-phase composite of mortar matrix,coarse aggregates,and the interfacial transition zone (ITZ) between the mortar matrix and the aggregates.The diffusion coefficient of chloride in the mortar and the ITZ can be analytically determined with only the water-to-cement ratio and volume fraction of fine aggregates.Fick's second law of diffusion was used as the governing equation for chloride diffusion in a homogenous medium (e.g.,mortar);it was discretized and applied to the truss network model.The solution procedure of the truss network model based on the diffusion law and the meso-scale composite structure of concrete is outlined.Additionally,the dependence of the diffusion coefficient of chloride in the mortar and the ITZ on exposure duration and temperature is taken into account to illustrate their effect on chloride diffusion coefficient.The numerical results show that the exposure duration and environmental temperature play important roles in the diffusion rate of chloride ions in concrete.It is also concluded that the meso-scale truss network model can be applied to chloride transport analysis of damaged (or cracked) concrete.

  19. Inhibition of herpes simplex virus type 1 entry by chloride channel inhibitors tamoxifen and NPPB

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Kai [Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou (China); College of Life Science and Technology, Jinan University, Guangzhou (China); Chen, Maoyun [Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou (China); College of pharmacy, Jinan University, Guangzhou (China); Xiang, Yangfei; Ma, Kaiqi [Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou (China); Jin, Fujun [Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou (China); College of pharmacy, Jinan University, Guangzhou (China); Wang, Xiao [School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006 (China); Wang, Xiaoyan; Wang, Shaoxiang [Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou (China); Wang, Yifei, E-mail: twang-yf@163.com [Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou (China)

    2014-04-18

    Highlights: • We analyze the anti-HSV potential of chloride channel inhibitors. • Tamoxifen and NPPB show anti-HSV-1 and anti-ACV-resistant HSV-1 activities. • HSV-1 infection induces intracellular chloride concentration increasing. • Tamoxifen and NPPB inhibit HSV-1 early infection. • Tamoxifen and NPPB prevent the fusion process of HSV-1. - Abstract: Herpes simplex virus type 1 (HSV-1) infection is very common worldwide and can cause significant health problems from periodic skin and corneal lesions to encephalitis. Appearance of drug-resistant viruses in clinical therapy has made exploring novel antiviral agents emergent. Here we show that chloride channel inhibitors, including tamoxifen and 5-nitro-2-(3-phenyl-propylamino) benzoic acid (NPPB), exhibited extensive antiviral activities toward HSV-1 and ACV-resistant HSV viruses. HSV-1 infection induced chloride ion influx while treatment with inhibitors reduced the increase of intracellular chloride ion concentration. Pretreatment or treatment of inhibitors at different time points during HSV-1 infection all suppressed viral RNA synthesis, protein expression and virus production. More detailed studies demonstrated that tamoxifen and NPPB acted as potent inhibitors of HSV-1 early entry step by preventing viral binding, penetration and nuclear translocation. Specifically the compounds appeared to affect viral fusion process by inhibiting virus binding to lipid rafts and interrupting calcium homeostasis. Taken together, the observation that tamoxifen and NPPB can block viral entry suggests a stronger potential for these compounds as well as other ion channel inhibitors in antiviral therapy against HSV-1, especially the compound tamoxifen is an immediately actionable drug that can be reused for treatment of HSV-1 infections.

  20. Performance optimization of coagulation/flocculation in the treatment of wastewater from a polyvinyl chloride plant.

    Science.gov (United States)

    Almubaddal, F; Alrumaihi, K; Ajbar, A

    2009-01-15

    This paper presents results of an experimental study of coagulation/flocculation process of wastewater generated from a polyvinyl chloride (PVC) plant. The wastewater contains fine chlorine-based solid materials (i.e. latex). Experiments were carried out using a model wastewater which is chemically identical to the actual plant but is more consistent. Inorganic ions (Al2(SO4)3, FeCl3 and CaCl2) and a water soluble commercial polyelectrolyte (PE) were added to the wastewater sample. Coagulation efficiency was determined by measuring both the turbidity of the supernatants and the relative settlement of the flocs in the jar test. It was found that aluminum and ferric ions were more efficient than calcium ions as coagulants. The addition of polyelectrolyte was found to improve substantially the coagulation/flocculation process. It was found that the (Al2(SO4)3) combined with the polyelectrolyte at certain pH and agitation speed gave the best results compared to calcium chloride or ferric chloride when combined with the same concentration of polyelectrolyte. Only 0.0375g of a solution of (0.5% Al2(SO4)3) was required to coagulate the model wastewater. Ferric chloride (2.5% FeCl3) combined with the polyelectrolyte, on the other hand, required 0.1g while the optimum turbidity is almost the same. As for calcium chloride (2.5% CaCl2) it was found to be the least effective. The coagulation/flocculation process was found to be dependent on both pH and the agitation speed.

  1. Effect of cracking and randomness of inputs on corrosion initiation of reinforced concrete bridge decks exposed to chlorides

    Directory of Open Access Journals (Sweden)

    P. Konecny

    2017-01-01

    Full Text Available The paper is aimed at the indicative evaluation of the effect of random scatter of input parameters in case of durability of reinforced concrete bridge deck. The time to onset of corrosion of steel reinforcement of concrete bridge deck exposed to chloride is evaluated. The effect of cracking in concrete onto chloride ingress is considered. The selected steel reinforcement protection strategies are: unprotected steel reinforcement, epoxy-coated steel reinforcement and water-proof barrier bellow asphalt overlay. The preliminary model for damage effect on chloride ion ingress through water proof membrane under penetrable asphalt overlay is used. 2-D finite element chloride ingress model is combined with Monte Carlo simulation technique. The innovative crack effect modeling via highly penetrable elements is applied. Deterministic and probabilistic calculations are compared.

  2. Catastrophic event modeling. [lithium thionyl chloride batteries

    Science.gov (United States)

    Frank, H. A.

    1981-01-01

    A mathematical model for the catastrophic failures (venting or explosion of the cell) in lithium thionyl chloride batteries is presented. The phenomenology of the various processes leading to cell failure is reviewed.

  3. Surface adsorption in strontium chloride ammines

    DEFF Research Database (Denmark)

    Ammitzbøll, Andreas L.; Lysgaard, Steen; Klukowska, Agata

    2013-01-01

    An adsorbed state and its implications on the ab- and desorption kinetics of ammonia in strontium chloride ammine is identified using a combination of ammonia absorption measurements, thermogravimetric analysis, and density functional theory calculations. During thermogravimetric analysis, ammoni...

  4. Qualitative Determination of Nitrate with Triphenylbenzylphosphonium Chloride.

    Science.gov (United States)

    Berry, Donna A.; Cole, Jerry J.

    1984-01-01

    Discusses two procedures for the identification of nitrate, the standard test ("Brown Ring" test) and a new procedure using triphenylbenzylphosphonium chloride (TPBPC). Effectiveness of both procedures is compared, with the TPBPC test proving to be more sensitive and accurate. (JM)

  5. Corneal Neurotoxicity Due to Topical Benzalkonium Chloride

    OpenAIRE

    Sarkar, Joy; Chaudhary, Shweta; Namavari, Abed; Ozturk, Okan; Chang, Jin-Hong; Yco, Lisette; Sonawane, Snehal; Khanolkar, Vishakha; Hallak, Joelle; Jain, Sandeep

    2012-01-01

    Topical application of benzalkonium chloride (BAK) to the eye causes dose-related corneal neurotoxicity. Corneal inflammation and reduction in aqueous tear production accompany neurotoxicity. Cessation of BAK treatment leads to recovery of corneal nerve density.

  6. Chloride Ingress into Concrete under Water Pressure

    DEFF Research Database (Denmark)

    Lund, Mia Schou; Sander, Lotte Braad; Grelk, Bent;

    2011-01-01

    The chloride ingress into concrete under water pressures of 100 kPa and 800 kPa have been investigated by experiments. The specimens were exposed to a 10% NaCl solution and water mixture. For the concrete having w/c = 0.35 the experimental results show the chloride diffusion coefficient at 800 k......Pa (~8 atm.) is 12 times greater than at 100 kPa (~1 atm.). For w/c = 0.45 and w/c = 0.55 the chloride diffusion coefficients are 7 and 3 times greater. This means that a change in pressure highly influences the chloride ingress into the concrete and thereby the life length models for concrete structures....

  7. 75 FR 20625 - Barium Chloride From China

    Science.gov (United States)

    2010-04-20

    ... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE COMMISSION Barium Chloride From China AGENCY: United States International Trade Commission. ACTION: Revised schedule for the subject review. DATES: Effective Date: April 9, 2010. FOR FURTHER INFORMATION CONTACT:...

  8. Role of chloride in the morphological evolution of organo-lead halide perovskite thin films.

    Science.gov (United States)

    Williams, Spencer T; Zuo, Fan; Chueh, Chu-Chen; Liao, Chien-Yi; Liang, Po-Wei; Jen, Alex K-Y

    2014-10-28

    A comprehensive morphological study was used to elucidate chloride's role in CH(3)NH(3)PbI(3-x)Cl(x) film evolution on a conducting polymer, PEDOT:PSS. Complex ion equilibria and aggregation in solution, as well as the role they play in nucleation, are found to ultimately be responsible for the unique morphological diversity observed in perovskite films grown in the presence of the chloride ion. An intermediate phase that is generated upon deposition and initial annealing templates continued self-assembly in the case of CH(3)NH(3)PbI(3-x)Cl(x). In the absence of chloride, the film growth of CH(3)NH(3)PbI(3) is directed by substrate interfacial energy. By employing the through-plane TEM analysis, we gain detailed insight into the unique crystallographic textures, grain structures, and elemental distributions across the breadth of films grown from precursor solutions with different chemistries. The lattice coherence seen in morphologies generated under the influence of chloride provides a physical rational for the enhancement in carrier diffusion length and lifetime.

  9. Telomerization of Vinyl Chloride with Chloroform Initiated by Ferrous Chloride-Dimethylacetamide under Ultrasonic Conditions

    Directory of Open Access Journals (Sweden)

    Hua Qian

    2015-01-01

    Full Text Available Telomerization of vinyl chloride with chloroform was investigated using ferrous chloride-dimethylacetamide system, and 42.1% yield, more than four times the one reported before, was achieved. The addition of ultrasound further improved the reaction and yield was raised to 51.9% with trace byproducts at highly reduced reaction time and temperature. Ferrous chloride-dimethylacetamide under ultrasonic irradiation acts as a very efficient catalyst system for the 1 : 1 telomerization.

  10. Effect of Ammonium Molybdate Inhibition on Corrosion Behaviour of Mild Steel in Chloride and Sulphide Media

    Directory of Open Access Journals (Sweden)

    Ayo S. Afolabi

    2010-10-01

    Full Text Available The corrosion inhibition of mild steel in 3.0 M sodium chloride and 0.5 M sodium sulphide using various concentrations of ammonium molybdate was investigated in this work. The inhibition effect of this reagent in these media was monitored by weight loss and pH measurements. The analyses of the weight loss results showed that the corrosion susceptibility of mild steel in 3.0 M sodium chloride was more pronounced than in 0.5 M of sodium sulphide due to the aggressive chloride ions in the former and the weak nature of the latter. Ammonium molybdate produced a better inhibition performance of mild steel in 0.5 M sodium suphide than in 3.0 M sodium chloride medium and the higher the concentration of ammonium molybdate the more the inhibition performance on mild steel in the media studied. Optimum inhibition was obtained at 2.5 M ammonium molybdate in both media. The pH values in chloride medium remained acidic throughout the exposure period while those of sulphide medium shifted to alkaline region with exposure time; an effect that was traceable to higher inhibition obtained in the latter medium.

  11. Non destructive determination of the free chloride content in cement based materials

    Energy Technology Data Exchange (ETDEWEB)

    Elsener, B. [Department of Inorganic and Analytical Chemistry, University of Cagliari, I-09128 Cagliari (Italy); Institute of Materials Chemistry and Corrosion, Swiss Federal Institute of Technology, ETH Hoenggerberg, CH-8093 Zuerich (Switzerland); Zimmermann, L.; Boehni, H. [Institute of Materials Chemistry and Corrosion, Swiss Federal Institute of Technology, ETH Hoenggerberg, CH-8093 Zuerich (Switzerland)

    2003-06-01

    A non-destructive chloride sensitive sensor element for use in cement based porous materials is presented. The sensor element determines the activity of the free chloride ions in solutions and in porous cement based materials such as cement paste, mortar or concrete. The calibration in synthetic pore solution showed a response according to Nernst law over three decades of chloride concentration. The sensor element has shown excellent reproducibility and long term stability. The sensor element has been used to monitor the chloride uptake into mortar specimens. The results show a good agreement between the free chloride content determined by the sensor and by pore water expression. Applications in monitoring of reinforced concrete structures and their limitations are discussed. (Abstract Copyright [2003], Wiley Periodicals, Inc.) [German] In der vorliegenden Arbeit wird ein Chloridsensor zur zerstoerungsfreien Erfassung des Chloridgehalts in zementoesen Materialien beschrieben. Der Sensor bestimmt die Aktivitaet der freien Chloridionen in Loesungen und in Zementstein, Moertel oder Beton. Die Kalibrierungskurve in synthetischer Betonporenloesung zeigt das erwartete Nernst'sche Verhalten ueber mehr als drei Konzentrationsdekaden. Der Sensor weist eine sehr hohe Reproduzierbarkeit und Langzeitstabilitaet auf. Der Chloridsensor wurde eingesetzt, um das Eindringen der Chloridionen in Moertelpruefkoerpern zu untersuchen. Ein Vergleich der Chloridkonzentration bestimmt durch Auspressen der Porenloesung am Ende der Versuche mit den von Sensoren bestimmten Chloridkonzentration zeigt eine sehr gute Uebereinstimmung. Praktische Anwendungen und die Einsatzgrenzen des Sensors werden diskutiert. (Abstract Copyright [2003], Wiley Periodicals, Inc.)

  12. Cesium chloride-induced torsades de pointes

    OpenAIRE

    Wiens, Matthew; Gordon, Wendy; Baulcomb, Daisy; Mattman, Andre; Mock, Tom; Brown, Robert

    2009-01-01

    The chloride salt of cesium, a group 1A element, is gaining popularity as an alternative treatment of advanced cancers. Cesium chloride has primarily been used in cardiovascular research for arrhythmogenesis in animals because of its potassium-blocking effects. The present report describes a 45-year-old woman with metastatic breast cancer who experienced repeated episodes of torsades de pointes polymorphic ventricular tachycardia after several months of oral cesium therapy. There was a clear ...

  13. The kinetics of the hydrogen chloride oxidation

    Directory of Open Access Journals (Sweden)

    Gonzalez Martinez Isai

    2013-01-01

    Full Text Available Hydrogen chloride (HCl oxidation has been investigated on technical membrane electrode assemblies in a cyclone flow cell. Influence of Nafion loading, temperature and hydrogen chloride mole fraction in the gas phase has been studied. The apparent kinetic parameters like reaction order with respect to HCl, Tafel slope and activation energy have been determined from polarization data. The apparent kinetic parameters suggest that the recombination of adsorbed Cl intermediate is the rate determining step.

  14. Ion-Ion Neutralization.

    Science.gov (United States)

    1980-12-31

    plasma were identified using a downstream quadrupole mass spectrometer. In these experimento it is a simple matter to establish H+(H 2 0):f as the...pressure as predicted by the Thomson t2rnary mechanism whicK hzr been suownr to be valid experimentally at hiTh rrsurs (,han and Peron, 1:EI4 hereafter t...of NO , NO2 ions in various gases and the ternary recombination coefficients of these ions in the higher pres:;ure ( Thomson ) re"ie. Equation (5) cr>n

  15. Ion Selectivity Mechanism in a Bacterial Pentameric Ligand-Gated Ion Channel

    Energy Technology Data Exchange (ETDEWEB)

    Fritsch, Sebastian M [ORNL; Ivanov, Ivaylo N [ORNL; Wang, Hailong [Mayo Clinic College of Medicine; Cheng, Xiaolin [ORNL

    2011-01-01

    The proton-gated ion channel from Gloeobacter violaceus (GLIC) is a prokaryotic homolog of the eukaryotic nicotinic acetylcholine receptor (nAChR) that responds to the binding of neurotransmitter acetylcholine and mediates fast signal transmission. Recent emergence of a high resolution crystal structure of GLIC captured in a potentially open state allowed detailed, atomic-level insight into ion conduction and selectivity mechanisms in these channels. Herein, we have examined the barriers to ion conduction and origins of ion selectivity in the GLIC channel by the construction of potential of mean force (PMF) profiles for sodium and chloride ions inside the transmembrane region. Our calculations reveal that the GLIC channel is open for a sodium ion to transport, but presents a ~10 kcal/mol free energy barrier for a chloride ion, which arises primarily from the unfavorable interactions with a ring of negatively charged glutamate residues (E-2 ) at the intracellular end and a ring of hydrophobic residues (I9 ) in the middle of the transmembrane domain. Our collective findings further suggest that the charge selection mechanism can, to a large extent, be attributed to the narrow intracellular end and a ring of glutamate residues in this position their strong negative electrostatics and ability to bind cations. By contrast, E19 at the extracellular entrance only plays a minor role in ion selectivity of GLIC. In addition to electrostatics, both ion hydration and protein dynamics are found to be crucial for ion conduction as well, which explains why a chloride ion experiences a much greater barrier than a sodium ion in the hydrophobic region of the pore.

  16. Analyzing ion distributions around DNA.

    Science.gov (United States)

    Lavery, Richard; Maddocks, John H; Pasi, Marco; Zakrzewska, Krystyna

    2014-07-01

    We present a new method for analyzing ion, or molecule, distributions around helical nucleic acids and illustrate the approach by analyzing data derived from molecular dynamics simulations. The analysis is based on the use of curvilinear helicoidal coordinates and leads to highly localized ion densities compared to those obtained by simply superposing molecular dynamics snapshots in Cartesian space. The results identify highly populated and sequence-dependent regions where ions strongly interact with the nucleic and are coupled to its conformational fluctuations. The data from this approach is presented as ion populations or ion densities (in units of molarity) and can be analyzed in radial, angular and longitudinal coordinates using 1D or 2D graphics. It is also possible to regenerate 3D densities in Cartesian space. This approach makes it easy to understand and compare ion distributions and also allows the calculation of average ion populations in any desired zone surrounding a nucleic acid without requiring references to its constituent atoms. The method is illustrated using microsecond molecular dynamics simulations for two different DNA oligomers in the presence of 0.15 M potassium chloride. We discuss the results in terms of convergence, sequence-specific ion binding and coupling with DNA conformation.

  17. Structure transitions between copper-sulphate and copper-chloride UPD phases on Au(111)

    Indian Academy of Sciences (India)

    Ilya V Pobelov; Gábor Nagy; Thomas Wandlowski

    2009-09-01

    Structure transitions between copper UPD adlayers on Au(111)-(1 × 1) in sulfuric acid and chloride containing electrolyte were investigated by in situ scanning tunnelling microscopy. We demonstrate that co-adsorbed sulphate ions in the (√3 × √3)R30° UPD adlayer are replaced by chloride ions and, depending on the halide coverage, a commensurate (2 × 2) or a slightly distorted (5 × 5)-like Cu-Cl UPD adlayer are formed. The stability ranges of these phases are controlled both by the electrode potential and the Cl- concentration. Phase transitions between the three UPD phases were monitored by time-resolved in situ STM. The observed structure details were attributed to mechanisms based on two-dimensional nucleation and growth processes.

  18. 42 CFR 84.250 - Vinyl chloride respirators; description.

    Science.gov (United States)

    2010-10-01

    ... 42 Public Health 1 2010-10-01 2010-10-01 false Vinyl chloride respirators; description. 84.250... Respirators § 84.250 Vinyl chloride respirators; description. Vinyl chloride respirators, including all... escape from vinyl chloride atmospheres containing adequate oxygen to support life, are...

  19. 3-Carbamoylquinoxalin-1-ium chloride

    Directory of Open Access Journals (Sweden)

    James K. Harper

    2012-01-01

    Full Text Available The title compound, C9H8N3O+·Cl−, was isolated from a liquid culture of streptomyces sp. In the cation, the ring system makes a dihedral angle of 0.2 (2° with the amide group. The protonation creating the cation occurs at ome of the N atoms in the quinoxaline ring system. In the crystal, the ions are linked through N—H...O and N—H...Cl hydrogen bonds, forming a two-dimensional network parallel to (10overline{3}.

  20. Theoretical predictions of novel potassium chloride phases under pressure.

    Science.gov (United States)

    Shamp, Andrew; Saitta, Patrick; Zurek, Eva

    2015-05-14

    Evolutionary structure searches predict two hitherto unknown phases of KCl that are the most stable in the pressure regime of 200-600 GPa. I41/amd-KCl, which has the lowest enthalpy between ∼200-350 GPa, can be thought of as being composed of two three-connected nets. This structure can be compared with that of the Cs-IV electride (Cs(+)e(-)): the potassium ions assume the positions of the cesium ions, and the chloride ions are found roughly in the regions of the valence electrons. Above ∼350 GPa a Pnma phase, which is isotypic with phases of CsH and CsI that are stable under pressure, becomes preferred. Just as in Pnma-CsI, the atoms in Pnma-KCl assume an hcp-like lattice; these alkali halides resemble the high-pressure structures of the isoelectronic noble gas solids Xe and Ar, respectively. The equation of state of KCl is extended to 600 GPa, enabling the use of this alkali halide as a pressure guage in ultra-high pressure static compression experiments. KCl is predicted to remain insulating to at least 420 GPa.

  1. Effect of Mercuric Chloride on Kinetic Properties of Horseradish Peroxidase

    Directory of Open Access Journals (Sweden)

    N Einollahi

    2006-06-01

    Full Text Available Mercury is one of the three major environmental metal poisons, and mercuric chloride is a highly reactive compound which can harm cells by a variety of mechanisms including direct interaction with sulphydryl groups of proteins and enzymes, therefore affecting the enzymatic activity. This study focused on the effect of Hg++ on horseradish peroxidase (donor: hydrogen peroxide oxidoreductase, EC 1.11.1.7 (HRP (Isoenzyme C activity. In the presence of 88 mM hydrogen peroxide Km for o-dianisidine oxidation was 0.05 millimolar and Vmax was 8.5 M.s-1. Incubation of the enzyme with 1 to 100 millimolar mercuric chloride for 5-20- and 60 min resulted in progressive inhibition of the enzymatic activity. At low Hg++ concentrations the inhibition was reversible by excess substrate, while at high Hg++ concentration the inhibition was not reversible. Results also indicated that the type of inhibition depended on the duration of incubation of the enzyme with metal ion and on the Hg++ concentration. So we could conclude that the type of inhibition changed from noncompetitive to mix with increased incubation time and increased metal concentration.

  2. Determinaciones termogravimétricas y de calor específico de un concentrado comercial de ulexita, entre temperatura ambiente y 1.000 ºC

    Directory of Open Access Journals (Sweden)

    Flores, H. R.

    2006-12-01

    Full Text Available The important amount of hydration water in the ulexite (NaCaB5O9.8H2O, allows using calcination methods to increase its B2O3 content. This paper analyses the thermal decomposition reaction of a preconcentrated ulexite through weight loss measurements, which occur during the heating of samples until 1000 ºC. Determinations of heat content at each temperature were made using an isoperibol calorimeter. The mean specific heat was calculated from these values, and its dependence on temperature was determined. The maximum weight loss was about 32.5 % and the specific heat obtained was 1,13 kJ/kgºC for solid samples and 1,38 kJ/kgºC for fluid samples.The results are useful for the design of the industrial process, in order to determine the thermal requirements for heating calcined ulexite, and to obtain smelted ulexite.

    El elevado contenido de agua de hidratación de la ulexita (NaCaB5O9.8H2O permite utilizar la calcinación como método de concentración. En este trabajo se analiza la reacción de descomposición térmica de un preconcentrado de ulexita a través de determinaciones de la pérdida de peso ocurrida durante el calentamiento de la muestra hasta 1000 ºC. Por otra parte, se ha determinado el valor del calor sensible a cada temperatura ensayada mediante un calorímetro tipo isoperibol y se ha calculado el calor específico medio de la muestra calcinada, así como su variación con la temperatura. Se obtuvieron pérdidas de peso de 32,5 % y valores del calor específico de 1,13 kJ/kgºC para muestras sólidas y 1,38 kJ/kgºC para las fluidas. Los resultados son de utilidad para el diseño del proceso industrial, para la determinación del requerimiento térmico para el calentamiento de ulexita calcinada y para la obtención de una frita.

  3. Phase and extraction equilibria in water-polyethyleneglycol ethers of monoethanolamides of synthetic fatty acid-ammonium chloride systems

    Science.gov (United States)

    Lesnov, A. E.; Golovkina, A. V.; Kudryashova, O. S.; Denisova, S. A.

    2016-08-01

    Phase equilibria in layering systems of water, polyethyleneglycol ethers of monoethanolamides of synthetic fatty acids (SFAs) (synthamide-5), and ammonium chloride are studied. The possibility of using such systems for the liquid extraction of metal ions is evaluated. The effect the nature of salting-out agents has on the processes of segregation of the systems has been considered.

  4. ARE MODELS OF ANION HYDRATION OVERBOUND ? THE SOLVATION OF THE ELECTRON AND CHLORIDE ANION COMPARED

    OpenAIRE

    Sprik, M.

    1991-01-01

    By means of a fully polarizable model for the chloride ion-water interaction we show that the modelling of anion solvation suffers from a similar inconsistency as the current electron-solvent potentials. Either the bulk hydration enthalpies are correct with the first hydration shell overbound, or the potential is adapted to describe the local environment of the solute at the expense of a major loss of solvation enthalpy. It is argued that boundary effects in the simulation are at least partly...

  5. Requirement for chloride channel function during the hepatitis C virus life cycle

    OpenAIRE

    Igloi, Z; Mohl, BP; Lippiat, JD; Harris, M.; Mankouri, J

    2015-01-01

    Hepatocytes express an array of plasma membrane and intracellular ion channels, yet their role during the hepatitis C virus (HCV) life cycle remains largely undefined. Here, we show that HCV increases intracellular hepatic chloride (Cl−) influx that can be inhibited by selective Cl− channel blockers. Through pharmacological and small interfering RNA (siRNA)-mediated silencing, we demonstrate that Cl− channel inhibition is detrimental to HCV replication. This represents the first observation o...

  6. Experimental Investigation on Pore Structure Characterization of Concrete Exposed to Water and Chlorides

    OpenAIRE

    LIU Jun; Tang, Kaifeng; Qiu, Qiwen; Pan, Dong; Lei, Zongru; Xing, Feng

    2014-01-01

    In this paper, the pore structure characterization of concrete exposed to deionised water and 5% NaCl solution was evaluated using mercury intrusion porosity (MIP), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The effects of calcium leaching, fly ash incorporation, and chloride ions on the evolution of pore structure characteristics were investigated. The results demonstrate that: (i) in ordinary concrete without any fly ash, the leaching effect of the cement products is mo...

  7. The Validation of Nematode-Specific Acetylcholine-Gated Chloride Channels as Potential Anthelmintic Drug Targets.

    Science.gov (United States)

    Wever, Claudia M; Farrington, Danielle; Dent, Joseph A

    2015-01-01

    New compounds are needed to treat parasitic nematode infections in humans, livestock and plants. Small molecule anthelmintics are the primary means of nematode parasite control in animals; however, widespread resistance to the currently available drug classes means control will be impossible without the introduction of new compounds. Adverse environmental effects associated with nematocides used to control plant parasitic species are also motivating the search for safer, more effective compounds. Discovery of new anthelmintic drugs in particular has been a serious challenge due to the difficulty of obtaining and culturing target parasites for high-throughput screens and the lack of functional genomic techniques to validate potential drug targets in these pathogens. We present here a novel strategy for target validation that employs the free-living nematode Caenorhabditis elegans to demonstrate the value of new ligand-gated ion channels as targets for anthelmintic discovery. Many successful anthelmintics, including ivermectin, levamisole and monepantel, are agonists of pentameric ligand-gated ion channels, suggesting that the unexploited pentameric ion channels encoded in parasite genomes may be suitable drug targets. We validated five members of the nematode-specific family of acetylcholine-gated chloride channels as targets of agonists with anthelmintic properties by ectopically expressing an ivermectin-gated chloride channel, AVR-15, in tissues that endogenously express the acetylcholine-gated chloride channels and using the effects of ivermectin to predict the effects of an acetylcholine-gated chloride channel agonist. In principle, our strategy can be applied to validate any ion channel as a putative anti-parasitic drug target.

  8. The Validation of Nematode-Specific Acetylcholine-Gated Chloride Channels as Potential Anthelmintic Drug Targets.

    Directory of Open Access Journals (Sweden)

    Claudia M Wever

    Full Text Available New compounds are needed to treat parasitic nematode infections in humans, livestock and plants. Small molecule anthelmintics are the primary means of nematode parasite control in animals; however, widespread resistance to the currently available drug classes means control will be impossible without the introduction of new compounds. Adverse environmental effects associated with nematocides used to control plant parasitic species are also motivating the search for safer, more effective compounds. Discovery of new anthelmintic drugs in particular has been a serious challenge due to the difficulty of obtaining and culturing target parasites for high-throughput screens and the lack of functional genomic techniques to validate potential drug targets in these pathogens. We present here a novel strategy for target validation that employs the free-living nematode Caenorhabditis elegans to demonstrate the value of new ligand-gated ion channels as targets for anthelmintic discovery. Many successful anthelmintics, including ivermectin, levamisole and monepantel, are agonists of pentameric ligand-gated ion channels, suggesting that the unexploited pentameric ion channels encoded in parasite genomes may be suitable drug targets. We validated five members of the nematode-specific family of acetylcholine-gated chloride channels as targets of agonists with anthelmintic properties by ectopically expressing an ivermectin-gated chloride channel, AVR-15, in tissues that endogenously express the acetylcholine-gated chloride channels and using the effects of ivermectin to predict the effects of an acetylcholine-gated chloride channel agonist. In principle, our strategy can be applied to validate any ion channel as a putative anti-parasitic drug target.

  9. The Validation of Nematode-Specific Acetylcholine-Gated Chloride Channels as Potential Anthelmintic Drug Targets

    Science.gov (United States)

    Wever, Claudia M.; Farrington, Danielle; Dent, Joseph A.

    2015-01-01

    New compounds are needed to treat parasitic nematode infections in humans, livestock and plants. Small molecule anthelmintics are the primary means of nematode parasite control in animals; however, widespread resistance to the currently available drug classes means control will be impossible without the introduction of new compounds. Adverse environmental effects associated with nematocides used to control plant parasitic species are also motivating the search for safer, more effective compounds. Discovery of new anthelmintic drugs in particular has been a serious challenge due to the difficulty of obtaining and culturing target parasites for high-throughput screens and the lack of functional genomic techniques to validate potential drug targets in these pathogens. We present here a novel strategy for target validation that employs the free-living nematode Caenorhabditis elegans to demonstrate the value of new ligand-gated ion channels as targets for anthelmintic discovery. Many successful anthelmintics, including ivermectin, levamisole and monepantel, are agonists of pentameric ligand-gated ion channels, suggesting that the unexploited pentameric ion channels encoded in parasite genomes may be suitable drug targets. We validated five members of the nematode-specific family of acetylcholine-gated chloride channels as targets of agonists with anthelmintic properties by ectopically expressing an ivermectin-gated chloride channel, AVR-15, in tissues that endogenously express the acetylcholine-gated chloride channels and using the effects of ivermectin to predict the effects of an acetylcholine-gated chloride channel agonist. In principle, our strategy can be applied to validate any ion channel as a putative anti-parasitic drug target. PMID:26393923

  10. Corrosion of LY12 aluminum alloy in sodium chloride solution

    Institute of Scientific and Technical Information of China (English)

    程英亮; 张昭; 曹发和; 李劲风; 张鉴清; 王建明; 曹楚南

    2003-01-01

    The corrosion behavior of LY12 alloy in sodium chloride solution and its electrochemical noise were reported. The development of the micro-pits on the alloy surface was monitored by scanning electron microscopy, scanning tunneling microscopy, and electrochemical noise method. All the measurements show that the corrosion of LY12 alloy can be divided into two stages: a very reactive initial stage and a relative constant stable stage. The initial stage is corresponded to the adsorption of Cl ions and its reaction with the oxide film and the dissolution of Mg containing particles. The stable stage is corresponded to the development of the micro-pits by the galvanic attack formed by Al-Fe-Cu-Mn containing particles and the matrix. The initial stage lasts about 2-3 h while the stable stage dominates the whole corrosion process.

  11. Structure of concentrated aqueous solutions of scandium chloride

    Science.gov (United States)

    Smirnov, P. R.; Grechin, O. V.

    2017-03-01

    It is shown via X-ray diffraction that aqueous solutions of scandium chloride form ionic associates in a wide range of concentrations. It is established that the Sc3+ ion coordination number increases upon dilution to 8.2 at an unchanged Sc3+-OH2 distance of 0.215 nm. The second coordination sphere of the cation forms at an average distance of 0.420 nm. The number of solvent molecules in the sphere logically increases during dilution. It is concluded that the anion does not form its own sphere in highly concentrated solutions. This coordination sphere begins to form only in solutions with moderate concentrations at a distance of 0.315 nm, and it contains six water molecules in diluted solutions.

  12. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    Directory of Open Access Journals (Sweden)

    H. Guan

    2009-09-01

    Full Text Available Chloride is commonly used as an environmental tracer for studying water flow and solute transport in the environment. It is especially useful for estimating groundwater recharge based on the commonly used chloride mass balance (CMB method. Strong spatial variability in chloride deposition in coastal areas is one difficulty encountered in appropriately applying the CMB approach. Furthermore, intensive vegetation clearance for agriculture, for example during the European settlement in many coastal areas of Australia, may have perturbed catchment chloride balance conditions for appropriate use in CMB applications. In order to deal with these issues, a high resolution chloride deposition map in the coastal region is needed. In this study, we examined geographic, orographic, and atmospheric factors influencing chloride deposition in the Mount Lofty Ranges (MLR, a coastal hilly area of approximately 9000 km2 spatial extent in South Australia, using partial correlation and regression analyses. The results indicate that coastal distance, and terrain aspect and slope are two most significant factors controlling chloride deposition. Coastal distance accounts for 65% spatial variability in chloride deposition, with terrain aspect and slope for 8%. The deposition gradient is about 0.08 gm-2 year-1 km-1 as one progresses inland. The results are incorporated into a published de-trended residual kriging approach (ASOADeK to produce a 1 km×1 km resolution annual chloride deposition map and a bulk precipitation chloride concentration map. The average uncertainty of the deposition map is about 30% in the western MLR, and over 50% in the eastern MLR. The maps will form a very useful basis for examining catchment chloride balances for use in the CMB application in the study area.

  13. Changes in ion transport in inflammatory disease

    Directory of Open Access Journals (Sweden)

    Eisenhut Michael

    2006-03-01

    Full Text Available Abstract Ion transport is essential for maintenance of transmembranous and transcellular electric potential, fluid transport and cellular volume. Disturbance of ion transport has been associated with cellular dysfunction, intra and extracellular edema and abnormalities of epithelial surface liquid volume. There is increasing evidence that conditions characterized by an intense local or systemic inflammatory response are associated with abnormal ion transport. This abnormal ion transport has been involved in the pathogenesis of conditions like hypovolemia due to fluid losses, hyponatremia and hypokalemia in diarrhoeal diseases, electrolyte abnormalites in pyelonephritis of early infancy, septicemia induced pulmonary edema, and in hypersecretion and edema induced by inflammatory reactions of the mucosa of the upper respiratory tract. Components of membranous ion transport systems, which have been shown to undergo a change in function during an inflammatory response include the sodium potassium ATPase, the epithelial sodium channel, the Cystic Fibrosis Transmembrane Conductance Regulator and calcium activated chloride channels and the sodium potassium chloride co-transporter. Inflammatory mediators, which influence ion transport are tumor necrosis factor, gamma interferon, interleukins, transforming growth factor, leukotrienes and bradykinin. They trigger the release of specific messengers like prostaglandins, nitric oxide and histamine which alter ion transport system function through specific receptors, intracellular second messengers and protein kinases. This review summarizes data on in vivo measurements of changes in ion transport in acute inflammatory conditions and in vitro studies, which have explored the underlying mechanisms. Potential interventions directed at a correction of the observed abnormalities are discussed.

  14. Effect of chloride introduction on the optical properties in Eu3+ -doped fluorozirconate glasses

    Science.gov (United States)

    Jin, Han; Mo, Zhao-Jun; Zhang, Xiao-Song; Yuan, Lin-Lin; Yan, Ming; Li, Lan

    2016-10-01

    Fluorozirconate glass containing Eu3+ ions and chloride ions are prepared by a meltquenching method. The luminescence behavior of Eu3+ affected by Cl ions is investigated. With increasing Cl ion concentration, the luminous intensity of Eu3+ is significantly enhanced and the quantum efficiency of fluorozirconate glass is improved. Meanwhile, the intensity parameter Ω 2 increases according to the Judd-Ofelt calculation, which indicates the decrease of local symmetry. The average lifetime of Eu3+ increases by introducing the Cl ions. Moreover, we find two kinds of sites for Eu3+ ions in a glass network by analyzing the fluorescence decay. The distribution of Eu3+ ions changes with increasing Cl ion concentration. In addition, the excessive Cl ions lead to the separation of the glass phase and the formation of the crystal phase, thus reducing the transmittance dramatically. Project supported by the National High Technology Research and Development Program of China (Grant No. 2013AA014201), the Natural Science Foundation of Tianjin, China (Grant Nos. 14JCZDJC31200, 15JCYBJC16700, and 15JCYBJC16800), the National Key Foundation for Exploring Scientific Instrument of China (Grant No. 2014YQ120351), and the International Cooperation Program from Science and Technology of Tianjin, China (Grant No. 14RCGHGX00872).

  15. Comparison of Inactivation and Unfolding of Calf Intestinal Alkaline Phosphatase in Guanidinium Chloride Solution

    Institute of Scientific and Technical Information of China (English)

    张英侠; 闫淑莲; 刘永利; 席宏伟; 周海梦

    2002-01-01

    The changes in activity and unfolding of calf intestinal alkaline phosphatase (CIP) during denaturation in guanidinium chloride solutions of different concentrations were investigated using ultraviolet difference absorption spectra and fluorescence emission spectra. Unfolding and inactivation rate constants were measured and compared. The inactivation course is much faster than that of unfolding, which suggests that the active site of CIP containing two zinc ions and one magnesium ion is situated in a limited and flexible region of the enzyme molecule, which is more fragile to the denaturant than the protein as a whole.

  16. Inhibition of nitrite-induced toxicity in channel catfish by calcium chloride and sodium chloride

    Science.gov (United States)

    Tommasso J.R., Wright; Simco, B.A.; Davis, K.B.

    1980-01-01

    Environmental chloride has been shown to inhibit methemoglobin formation in fish, thereby offering a protective effect against nitrite toxicity. Channel catfish (Ictalurus punctatus) were simultaneously exposed to various environmental nitrite and chloride levels (as either CaCl2 or NaCl) in dechlorinated tap water (40 mg/L total hardness, 47 mg/L alkalinity, 4 mg/L chloride, pH = 6.9-7.1, and temperature 21-24°C). Methemoglobin levels in fish simultaneously exposed to 2.5 mg/L nitrite and up to 30 mg/L chloride as either CaCl2 or NaCl were similar but significantly lower than in unprotected fish. Exposure to 10 mg/L nitrite and 60 mg/L chloride resulted in methemoglobin levels similar to those of the controls; most unprotected fish died. Fish exposed to 10 mg/L nitrite had significantly lower methemoglobin levels when protected with 15.0 mg/L chloride as CaCl2 than with NaCl. Fish exposed to nitrite in the presence of 60 mg/L chloride (as either CaCl2 or NaCl) had similar 24-h LC50 values that were significantly elevated above those obtained in the absence of chloride. Calcium had little effect on tolerance to nitrite toxicity in channel catfish in contrast to its large effect reported in steelhead trout (Salmo gairdneri).

  17. Congenital Chloride Diarrhea: Diagnosis by Easy-Accessible Chloride Measurement in Feces

    Directory of Open Access Journals (Sweden)

    C. Gils

    2016-01-01

    Full Text Available Background. Congenital chloride diarrhea (CCD is an autosomal recessive disorder caused by mutations in the genes encoding the intestinal Cl−/HCO3- exchanger and is clinically characterized by watery, profound diarrhea, electrolyte disturbances, and metabolic alkalosis. The CCD diagnosis is based on the clinical symptoms and measurement of high chloride concentration in feces (>90 mmol/L and is confirmed by DNA testing. Untreated CCD is lethal, while long-term clinical outcome improves when treated correctly. Case Presentation. A 27-year-old woman had an emergency caesarian due to pain and discomfort in gestational week 36 + 4. The newborn boy had abdominal distension and yellow fluid per rectum. Therapy with intravenous glucose and sodium chloride decreased his stool frequency and improved his clinical condition. A suspicion of congenital chloride diarrhea was strongly supported using blood gas analyzer to measure an increased chloride concentration in the feces; the diagnosis was confirmed by DNA testing. Discussion. Measurement of chloride in feces using an ordinary blood gas analyzer can serve as a preliminary analysis when congenital chloride diarrhea is suspected. This measurement can be easily performed with a watery feces composition. An easy-accessible chloride measurement available will facilitate the diagnostics and support the initial treatment if CCD is suspected.

  18. Amine and Titanium (IV Chloride, Boron (III Chloride or Zirconium (IV Chloride-Promoted Baylis-Hillman Reactions

    Directory of Open Access Journals (Sweden)

    Shi-Cong Cui

    2001-10-01

    Full Text Available The Baylis-Hillman reactions of various aryl aldehydes with methyl vinyl ketone at temperatures below -20oC using Lewis acids such as titanium (IV chloride, boron (III chloride or zirconium (IV chloride in the presence of a catalytic amount of selected amines used as a Lewis bases afford the chlorinated compounds 1 as the major product in very high yields. Acrylonitrile can also undergo the same reaction to give the corresponding chlorinated product in moderate yield. A plausible reaction mechanism is proposed. However, if the reaction was carried out at room temperature (ca. 20oC, then the Z-configuration of the elimination product 3, derived from 1, was formed as the major product.

  19. Mitigation of chloride and sulfate based corrosion in reinforced concrete via electrokinetic nanoparticle treatment

    Science.gov (United States)

    Kupwade-Patil, Kunal

    barrier that formed primarily at the reinforcement surface where it inhibited the ingress of chlorides. When applied to sulfate attack, EN treatment was found to extract sulfate ions. This treatment also reduced porosity and increased concrete strength. The strength increases were limited by the accumulation of spallation damage that was accrued during the sulfate exposure period of the work. This demonstrated that treatment for sulfate attack was best suited to early stages of degradation or as a preventive measure.

  20. Electrochemical extraction of samarium from molten chlorides in pyrochemical processes

    Energy Technology Data Exchange (ETDEWEB)

    Castrillejo, Y., E-mail: ycastril@qa.uva.es [QUIANE/Dept Quimica Analitica, F. de Ciencias, Universidad de Valladolid, Prado de la Magdalena s/n, 47005 Valladolid (Spain); Fernandez, P. [QUIANE/Dept Quimica Analitica, F. de Ciencias, Universidad de Valladolid, Prado de la Magdalena s/n, 47005 Valladolid (Spain); Medina, J. [Dept Fisica Materia Condensada Cristalografia y Mineralogia, F. de Ciencias, Universidad de Valladolid, Prado de la Magdalena s/n, 47005 Valladolid (Spain); Hernandez, P. [Centro de Investigaciones Quimicas, Universidad Autonoma del Estado de Hidalgo, Carr. Pachuca-Tulancingo Km. 4.5, C.P. 42076 Pachuca, Hidalgo (Mexico); Barrado, E. [QUIANE/Dept Quimica Analitica, F. de Ciencias, Universidad de Valladolid, Prado de la Magdalena s/n, 47005 Valladolid (Spain)

    2011-10-01

    This work concerns the electrochemical extraction of samarium from molten chlorides. In this way, the electrochemical behaviour of samarium ions has been investigated in the eutectic LiCl-KCl at the surface of tungsten, aluminium and aluminium coated tungsten electrodes. On a W inert electrode the electro-reduction of Sm(III) takes place in only one soluble-soluble electrochemical step Sm(III)/Sm(II). The electrochemical system Sm(II)/Sm(0) has not been observed within the electrochemical window, because of the prior reduction of Li(I) ions from the solvent, which inhibits the electro-extraction of Sm species from the salt on such a substrate. Sm metal in contact with the melt react to give Li(0) according to the reaction: Sm(0) + 2Li(I) {r_reversible} Sm(II) + 2Li(0). On the contrary, on reactive Al electrodes the electrochemical system Sm(II)/Sm(0) was observed within the electroactive range. The potential shift of the redox couple is caused by the decrease of Sm activity in the metal phase due to the formation of Sm-Al alloys at the interface. The formation mechanism of the intermetallic compounds was studied in a melt containing: (i) both Sm(III) and Al(III) ions, using W and Al coated tungsten electrodes, and (ii) Sm(III) ions using an Al electrode. Analysis of the samples after potentiostatic electrolysis by X-ray diffraction and scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDS), allowed the identification of Al{sub 3}Sm and Al{sub 2}Sm.

  1. Efficient cellulose solvent: quaternary ammonium chlorides.

    Science.gov (United States)

    Kostag, Marc; Liebert, Tim; El Seoud, Omar A; Heinze, Thomas

    2013-10-01

    Pure quaternary tetraalkylammonium chlorides with one long alkyl chain dissolved in various organic solvents constitute a new class of cellulose solvents. The electrolytes are prepared in high yields and purity by Menshutkin quaternization, an inexpensive and easy synthesis route. The pure molten tetraalkylammonium chlorides dissolve up to 15 wt% of cellulose. Cosolvents, including N,N-dimethylacetamide (DMA), may be added in large excess, leading to a system of decreased viscosity. Contrary to the well-established solvent DMA/LiCl, cellulose dissolves in DMA/quaternary ammonium chlorides without any pretreatment. Thus, the use of the new solvent avoids some disadvantages of DMA/LiCl and ionic liquids, the most extensively employed solvents for homogeneous cellulose chemistry.

  2. Alkali metal and ammonium chlorides in water and heavy water (binary systems)

    CERN Document Server

    Cohen-Adad, R

    1991-01-01

    This volume surveys the data available in the literature for solid-fluid solubility equilibria plus selected solid-liquid-vapour equilibria, for binary systems containing alkali and ammonium chlorides in water or heavy water. Solubilities covered are lithium chloride, sodium chloride, potassium chloride, rubidium chloride, caesium chloride and ammonium chloride in water and heavy water.

  3. A study on the calcium chloride resistance of concrete containing an expansive additive[ACI SP-234-26

    Energy Technology Data Exchange (ETDEWEB)

    Akihiro, H.; Hiroyuki, K. [Denki Kagaku Kogyo Co. Ltd., Niigata (Japan); Masanobu, A. [Research Center of Inorganic Materials (Japan); Tsutomu, F. [Toyo Univ., Tokyo (Japan). Dept. of Civil and Environmental Engineering

    2006-07-01

    The addition of expansive additives to concrete helps to prevent cracks resulting from shrinkage and thermal stress. Chloride based deicing chemicals are used on roads during freezing conditions to prevent wheel slipping. This presentation discussed the damaging effects of salts on concrete prepared with a small amount of expansive additives. This experiment tested the chloride resistance of expansive-cement concrete mixtures made of an ordinary portland cement and a blast-furnace slag cement with and without an expansive additive based on a free CaO hydration as well as ettringite formation. Calcium chloride spray was used as a source of chloride ions. The objective was to determine if the addition of expansive additive had any affect on the chloride resistance of concrete. Details of the experiment were provided with reference to materials used, mix proportions, curing, testing for compression strength, depth of neutralization, measuring for change in length of concrete, pore size distribution, and microstructural observations. The study found that there were no adverse effects on the compressive strength, changes in length, or chloride penetration depth after the concrete was subjected to salt spray between 28 and 56 days of curing. 6 refs., 4 tabs., 4 figs.

  4. Hazards of lithium thionyl chloride batteries

    Science.gov (United States)

    Parry, J. M.

    1978-01-01

    Two different topics which only relate in that they are pertinent to lithium thionyl chloride battery safety are discussed. The first topic is a hazards analysis of a system (risk assessment), a formal approach that is used in nuclear engineering, predicting oil spills, etc. It is a formalized approach for obtaining assessment of the degree of risk associated with the use of any particular system. The second topic is a small piece of chemistry related to the explosions that can occur with lithium thionyl chloride systems. After the two topics are presented, a discussion is generated among the Workshop participants.

  5. EVALUATION OF BACTERICIDAL EFFECTIVENESS OF BENZALKONIUM CHLORIDE

    Directory of Open Access Journals (Sweden)

    K. Imandel

    1996-06-01

    Full Text Available Benzalkonium chloride is a quaternary ammounium Compounds derivative under different names such as Afxhang, Hamoon, Mahan etc, which have great and expanded use in sanitation and medical affairs. Bactericidal activity of these disinfectants was fulfilled according to National Standard Method No.2842 on Staph. Aureus, Sal. Typhimouium and E. coli. This laboratory test showed that, except Mahan that has not bactericidal efficacy on E.coli at concentration 0.4 percent, other disinfectants under the study in concentrations of 0.4, 0.8, 1, 1.2 percent have reliable antibacterial properties, and bacterial resistance to benzalkonium chloride has not occurred yet.

  6. Cesium chloride-induced torsades de pointes.

    Science.gov (United States)

    Wiens, Matthew; Gordon, Wendy; Baulcomb, Daisy; Mattman, Andre; Mock, Tom; Brown, Robert

    2009-09-01

    The chloride salt of cesium, a group 1A element, is gaining popularity as an alternative treatment of advanced cancers. Cesium chloride has primarily been used in cardiovascular research for arrhythmogenesis in animals because of its potassium-blocking effects. The present report describes a 45-year-old woman with metastatic breast cancer who experienced repeated episodes of torsades de pointes polymorphic ventricular tachycardia after several months of oral cesium therapy. There was a clear temporal relationship between cesium ingestion and the arrhythmia, which later resolved following discontinuation of cesium therapy. Serial cesium plasma and whole blood levels were measured over the ensuing six months and pharmacokinetic analysis was performed.

  7. Dielectric breakdown during Cs+ sputtering of polyvinyl chloride

    Science.gov (United States)

    Wahoud, F.; Guillot, J.; Audinot, J. N.; Bertrand, P.; Delcorte, A.; Migeon, H. N.

    2014-02-01

    Thin films of insulating polymers are sometimes analyzed by secondary ion mass spectrometry (SIMS) or by X-ray photoelectron spectroscopy (XPS) without the use of an electron gun. In this work, both SIMS and XPS have been used to study the chemical and structural modifications due to the charge effect during Cs+ sputtering of a thin film of polyvinyl chloride (PVC). The kinetic energy distribution study shows that at a small primary fluence ˜1015 Cs+ ions/cm2, the dielectric breakdown voltage of the PVC film is reached, i.e. the minimum voltage that causes a portion of an insulator to become electrically conductive. XPS study indicates that the conducting phase created in the PVC film after energetic Cs+ bombardment consists of graphitized carbon and metallic cesium clusters. After the dielectric breakdown of the film, the positive charge, previously accumulated on the surface, is neutralized through the conductive regions, which are created in the insulating film. During Cs+ sputtering of a PVC film, the chemical structure of the analyzed surface is completely modified and some ionic bonds such as CsC and CsCl are also created.

  8. Electrochemistry of ytterbium (III) in molten alkali metal chlorides

    Energy Technology Data Exchange (ETDEWEB)

    Smolenski, V.; Novoselova, A. [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, Ekaterinburg, 620219 (Russian Federation); Osipenko, A. [Research Institute of Atomic Reactors, Dimitrovgrad-10, Ulyanovsk Region, 433010 (Russian Federation); Caravaca, C. [High Level Waste Unit, Nuclear Fission Division, CIEMAT, Madrid, 28040 (Spain); Cordoba, G. de [High Level Waste Unit, Nuclear Fission Division, CIEMAT, Madrid, 28040 (Spain)], E-mail: g.cordoba@ciemat.es

    2008-12-30

    This work presents the electrochemical study of Yb(III) ions in molten alkali metal chlorides in the temperature range 723-1073 K. Transient electrochemical techniques such as linear sweep, cyclic and square wave voltammetry, and potentiometry at zero current have been used to investigate the reduction mechanism, transport parameters and thermodynamic properties of the reaction YbCl{sub 2} + 1/2Cl{sub 2} = YbCl{sub 3} The results obtained show that the reduction reaction Yb(III) + e{sup -} {r_reversible} Yb(II) is reversible being controlled by the rate of the mass transfer. The diffusion coefficient of [YbCl{sub 6}]{sup 3-} complex ions has been determined at different temperatures in the fused eutectic LiCl-KCl, the equimolar NaCl-KCl and the CsCl media. The apparent standard potential of the soluble-soluble redox system Yb(III)/Yb(II) has been obtained by cyclic voltammetry. The influence of the nature of the solvent on the electrochemical and thermodynamic properties of ytterbium compounds is discussed.

  9. Simulation-based Analysis of the Differences in the Removal Rate of Chlorides, Nitrates and Sulfates by Electrokinetic Desalination Treatments

    DEFF Research Database (Denmark)

    Paz-Garcia, Juan Manuel; Johannesson, Björn; Ottosen, Lisbeth M.;

    2012-01-01

    Due to their abundance in the natural environment, chloride, nitrate and sulfate salts are considered the main responsible for the salt-induced decay processes in building materials and sculptures. Electro-desalination techniques, enhanced with carbonated clay buffer poultice placed between...... than chlorides and nitrates. A physicochemical model for electrochemically-induced reactive-transport processes is described and used for a theoretical analysis of the influence of the chemical interactions on the removal rate of the target ions. Simulations for the electro-desalination of a brick...

  10. Deconvoluting the memory effect in Pd-catalyzed allylic alkylation; effect of leaving group and added chloride

    DEFF Research Database (Denmark)

    Fristrup, Peter; Jensen, Thomas; Hoppe, Jakob;

    2006-01-01

    An analysis of product distributions in the Tsuji-Trost reaction indicates that several instances of reported memory effects can be attributed to slow interconversion of the initially formed syn- and anti-[Pd(eta3-allyl)] complexes. Addition of chloride triggers a true memory effect, in which...... the allylic terminus originally bearing the leaving group has a higher reactivity. The latter effect, termed regioretention, can be rationalized by ionization from a palladium complex bearing a chloride ion, forming an unsymmetrically substituted [Pd(eta3-allyl)] complex. DFT calculations verify...

  11. Chloride adsorption by calcined layered double hydroxides in hardened Portland cement paste

    KAUST Repository

    Yoon, Seyoon

    2014-06-01

    This study investigated the feasibility of using calcined layered double hydroxides (CLDHs) to prevent chloride-induced deterioration in reinforced concrete. CLDHs not only adsorbed chloride ions in aqueous solution with a memory effect but also had a much higher binding capacity than the original layered double hydroxides (LDHs) in the cement matrix. We investigated this adsorption in hardened cement paste in batch cultures to determine adsorption isotherms. The measured and theoretical binding capacities (153 mg g -1 and 257 mg g-1, respectively) of the CLDHs were comparable to the theoretical capacity of Friedel\\'s salt (2 mol mol-1 or 121 mg g-1), which belongs to the LDH family among cementitious phases. We simulated chloride adsorption by CLDHs through the cement matrix using the Fickian model and compared the simulation result to the X-ray fluorescence (XRF) chlorine map. Based on our results, it is proposed that the adsorption process is governed by the chloride transport through the cement matrix; this process differs from that in an aqueous solution. X-ray diffraction (XRD) analysis showed that the CLDH rebuilds the layered structure in a cementitious environment, thereby demonstrating the feasibility of applying CLDHs to the cement and concrete industries. © 2014 Published by Elsevier B.V. All rights reserved.

  12. Removal of As(V), Cr(III) and Cr(VI) from aqueous environments by poly(acrylonitril-co-acrylamidopropyl-trimethyl ammonium chloride)-based hydrogels.

    Science.gov (United States)

    Dudu, Tuba Ersen; Sahiner, Mehtap; Alpaslan, Duygu; Demirci, Sahin; Aktas, Nahit

    2015-09-15

    Cationic poly(Acrylonitril-co-Acrylamidopropyl-trimethyl Ammonium Chloride) (p(AN-co-APTMACl)) hydrogels in bulk were synthesized by using acrylonitrile (AN) and 3-acrylamidopropyl-trimethyl ammonium chloride (APTMACl) as monomers. The prepared hydrogels were exposed to amidoximation reaction to replace hydrophobic nitrile groups with hydrophilic amidoxime groups that have metal ion binding ability. Those replacements were increased the hydrogels absorption capacity for As(V) and Cr(VI). Langmuir and Freundlich isotherms equations were utilized to obtain the best-fitted isotherm model for the absorption of the ions at different metal ion concentrations. The absorption data of As(V) ion were fitted well to Freundlich isotherm while those of Cr(VI) and Cr(III) ions were fitted well to Langmuir isotherm. The maximum absorption of poly(3-acrylamidopropyl-trimethyl ammonium chloride (p(APTMACl)) and amid-p(AN-co-APTMACl) macro gels were 22.39 mg and 21.83 mg for As(V), and 30.65 mg and 18.16 mg for Cr(VI) ion per unit gram dried gel, respectively. Kinetically, the absorption behaviors of Cr(III) and Cr(VI) ions were fitted well to a pseudo 2nd-order kinetic model and those of As(V) ions were fitted well to a pseudo 1st order kinetic model.

  13. Solvothermal synthesis of strontium phosphate chloride nanowire

    Science.gov (United States)

    Lam, W. M.; Wong, C. T.; Li, Z. Y.; Luk, K. D. K.; Chan, W. K.; Yang, C.; Chiu, K. Y.; Xu, B.; Lu, W. W.

    2007-08-01

    Strontium phosphate chloride nanowire was synthesized via a solvothermal treatment of strontium tri-polyphosphate and Collin salt in 1,4-dioxane at 150 °C. The effects of 1,4-dioxane concentration on particle morphology, crystallinity and phase purity were investigated in this study. The specimen morphology was analyzed by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). When the concentration of 1,4-dioxane was below 10%, micron-sized whisker was the dominant form. At 20-25% concentration of 1,4-dioxane, strontium phosphate chloride single-crystalline nanowire was 31±12 nm in diameter and 1.43±0.6 μm in length with an aspect ratio of 52.28±29.41. X-ray diffraction (XRD) pattern of this nanowire matched with that of strontium phosphate chloride (JCPDS #083-0973). When 1,4-dioxane concentration exceeded 25%, nanorod aggregate was the dominant form instead of nanowire. At 20-25% 1,4-dioxane concentration suitable strontium concentration combine with high chemical potential environment favors the formation of nanowires. By adding 1,4-dioxane impure phase such as β-strontium hydrogen phosphate, nanorod formation was suppressed. This method provides an efficient way to synthesize high aspect ratio strontium phosphate chloride nanowire. It has potential bioactive nanocomposite, high mechanical performance bioactive bone cement filler and fluorescent material applications.

  14. Influence of compaction on chloride ingress

    NARCIS (Netherlands)

    Zlopasa, J.

    2012-01-01

    Experiences from practice show the need for more of an understanding and optimization of the compaction process in order to design a more durable concrete structure. Local variations in compaction are very often the reason for initiation of local damage and initiation of chloride induced corrosion.

  15. Liquid crystalline critical dynamics in decylammonium chloride

    CERN Document Server

    Lee, K W; Lee, C E; Kang, K H; Rhee, C; Kang, J K

    1999-01-01

    Collective chain dynamics and phase transitions in a model biomembrane, decylammonium chloride (C sub 1 sub 0 H sub 2 sub 1 NH sub 3 Cl), were studied by means of proton nuclear magnetic resonance. Our measurements sensitively reflect the critical dynamics associated with the smectic C to smectic A transition of the lipid bilayer.

  16. Chloride migration in concrete with superabsorbent polymers

    DEFF Research Database (Denmark)

    Hasholt, Marianne Tange; Jensen, Ole Mejlhede

    2015-01-01

    Superabsorbent polymers (SAP) can be used as a means for internal curing of concrete. In the present study, the development of transport properties of concrete with SAP is investigated. The chloride migration coefficient according to NT BUILD 492 is used as a measure of this. Twenty concrete mixt...

  17. Gebromeerde vlamvertragers en broomdioxines in Choline Chloride

    NARCIS (Netherlands)

    Egmond, van H.J.; Traag, W.A.; Hoogenboom, L.A.P.

    2008-01-01

    Sinds begin 2008 worden in het Nationaal Plan Diervoeder Choline Chloride monsters (= diervoeder additief) gevonden waarbij de DR CALUX screenings-assay een sterk verdacht signaal geeft, maar bij de GC-HRMS geen dioxines en dl-PCB's worden gevonden. Dit rapport beschrijft de resultaten van nader ond

  18. 21 CFR 582.3845 - Stannous chloride.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Stannous chloride. 582.3845 Section 582.3845 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Chemical Preservatives §...

  19. 29 CFR 1910.1017 - Vinyl chloride.

    Science.gov (United States)

    2010-07-01

    ... possible exposure conditions. (2) Protective garments shall be provided clean and dry for each use. (i... Required Authorized Personnel Only (3) Containers of polyvinyl chloride resin waste from reactors or other... which may be useful: A. For kidney dysfunction: urine examination for albumin, red blood cells,...

  20. Spatial variability of chloride in concrete within homogeneously exposed areas

    NARCIS (Netherlands)

    Angst, U.M.; Polder, R.B.

    2014-01-01

    The concept of variability is increasingly considered in service life predictions. This paper reports experimental data on the spatial distribution of chloride in uncracked concrete subjected to homogeneous exposure. Chloride concentrations were measured with potentiometric sensors embedded in concr

  1. Viscosity and density tables of sodium chloride solutions

    Energy Technology Data Exchange (ETDEWEB)

    Fair, J.A.; Ozbek, H. (comps.)

    1977-04-01

    A file is presented containing tabulated data extracted from the scientific literature on the density and viscosity of aqueous sodium chloride solutions. Also included is a bibliography of the properties of aqueous sodium chloride solutions. (MHR)

  2. Adsorption of Chloride,Nitrate and Perchlorate by Variable Charge Soils

    Institute of Scientific and Technical Information of China (English)

    JIGUO-LIANG; KONGXIAO-LING

    1992-01-01

    Two cells consisting of a chloride-selective eloectrode and a nitrate-selective electrode or of a chloride-selectrive electrode and a perchlorate-selective electrode were directly put in the soil suspension to determine the concentration rations Cl-/NO3- or Cl-/ClO4- for studying the adsorption of the three anions by variable charge soils.It was found that all the concentration ration CCl-/CNO3- and CCl-/CClO4- in suspension were smaller than unity when soil samples were in equilibrium with mixed KCl and KNO3 or KCl and KClO4 solutions of equal concentration.The order of the amount of chloride,nitrate and perchlorate adsorbed by variable charge soils was Cl->NO3->ClO4- when the soils adsorbed these anions from the solution containing equal concentrations of Cl-,NO3- and ClO4-.Such factors as the pH of the suspension,the iron oxide content of the soil etc.Could affect the amounts and the ratios of anions adsorbed.The adsorption was chiefly caused by coulombic attraction,but a covalent force between the anion and the metal atom on the surface of soil particles may also be involved,at least for Cl- ions,even for NO3- ions.

  3. Critical pitting temperature for Type 254 SMO stainless steel in chloride solutions

    Energy Technology Data Exchange (ETDEWEB)

    Abd El Meguid, E.A. [Department of Electrochemistry and Corrosion, National Research Centre, Dokki, Cairo (Egypt)]. E-mail: eameguid_nrc@yahoo.com; Abd El Latif, A.A. [Department of Electrochemistry and Corrosion, National Research Centre, Dokki, Cairo (Egypt)

    2007-02-15

    The variation with time of the open circuit potential of high molybdenum containing stainless steel (Type 254 SMO) was measured in 4% sodium chloride solution in the temperatures range 30-100 deg. C. The plot of steady state potentials as function of temperature showed an inflection at 50 deg. C, attributed to the decrease of oxygen solubility in test solution above 50 deg. C. Potentiodynamic cycling anodic polarization technique was used to determine the critical pitting potential (E {sub pit}) and the critical protection potential (E {sub prot}) of the steel in 4-30% NaCl solutions at temperatures between 30 and 100 deg. C. By plotting the two values versus solution temperature, the corresponding critical pitting (CPT) and the critical protection (CPrT) temperatures were determined. Both parameters decreased with increasing chloride content. Above the CPT, E {sub pit} and E {sub prot} decreased linearly with log[Cl{sup -}]. The addition of bromide ions to the solution shifted both E {sub pit} and E {sub prot} towards positive values. In 4% NaCl, E {sub pit} increased linearly with pH in the range 1-10. The combined effect of chloride ion concentration and pH on the morphology of the pits was examined by scanning electron microscopy (SEM) following potentiodynamic cycling anodic polarization.

  4. Investigation of factors influencing chloride extraction efficiency during electrochemical chloride extraction from reinforcing concrete

    Science.gov (United States)

    Sharp, Stephen R.

    2005-11-01

    Electrochemical chloride extraction (ECE) is an accelerated bridge restoration method similar to cathodic protection, but operates at higher current densities and utilizes a temporary installation. Both techniques prolong the life of a bridge by reducing the corrosion rate of the reinforcing bar when properly applied. ECE achieves this by moving chlorides away from the reinforcement and out of the concrete while simultaneously increasing the alkalinity of the electrolyte near the reinforcing steel. Despite the proven success, significant use of ECE has not resulted in part due to an incomplete understanding in the following areas: (1) An estimation of the additional service life that can be expected following treatment when the treated member is again subjected to chlorides; (2) The cause of the decrease in current flow and, therefore, chloride removal rate during treatment; (3) Influence of water-to-cement (w/c) ratio and cover depth on the time required for treatment. This dissertation covers the research that is connected to the last two areas listed above. To begin examining these issues, plain carbon steel reinforcing bars (rebar) were embedded in portland cement concrete slabs of varying water-to-cement (w/c) ratios and cover depths, and then exposed to chlorides. A fraction of these slabs had sodium chloride added as an admixture, with all of the slabs subjected to cyclical ponding with a saturated solution of sodium chloride. ECE was then used to remove the chlorides from these slabs while making electrical measurements in the different layers between the rebar (cathode) and the titanium mat (anode) to follow the progress of the ECE process. During this study, it was revealed that the resistance of the outer concrete surface layer increases during ECE, inevitably restricting current flow, while the resistance of the underlying concrete decreases or remains constant. During ECE treatment, a white residue formed on the surface of the concrete. Analyses of the

  5. Aspergilli Response to Benzalkonium Chloride and Novel-Synthesized Fullerenol/Benzalkonium Chloride Nanocomposite

    OpenAIRE

    Nikola Unković; Milica Ljaljević Grbić; Miloš Stupar; Jelena Vukojević; Vesna Janković; Danica Jović; Aleksandar Djordjević

    2015-01-01

    A comprehensive comparative analysis of antifungal potential of benzalkonium chloride and newly synthesized fullerenol/benzalkonium chloride nanocomposite was conducted to assess the possible impact of carbon-based nanocarrier on antimicrobial properties of the commonly used biocide. Physical characterization of synthesized nanocomposite showed zeta potential of +37.4 mV and inhomogeneous particles size distribution, with nanocomposite particles’ dimensions within 30–143 nm and maximum number...

  6. Prenatal susceptibility to carcinogenesis by xenobiotic substances including vinyl chloride.

    OpenAIRE

    Rice, J M

    1981-01-01

    The carcinogenicity of vinyl chloride for experimental animals when administered transplacentally is reviewed in comparison with known transplacental carcinogens, including those that, like vinyl chloride, are dependent on enzyme-mediated metabolic conversion to a reactive intermediate in maternal or fetal tissues. Vinyl chloride is converted by mixed-function oxidases to the reactive metabolite chlorooxirane, the carcinogenicity of which is also reviewed. Vinyl chloride is unequivocally a tr...

  7. Sodium and chloride levels in rainfall, mist, streamwater and groundwater at the Plynlimon catchments, mid-Wales: inferences on hydrological and chemical controls

    Directory of Open Access Journals (Sweden)

    C. Neal

    2000-01-01

    Full Text Available Variations in sodium and chloride in atmospheric inputs (rainfall and mist, stream runoff and groundwater stores are documented for the upper Severn River (Afon Hafren and Afon Hore catchments, Plynlimon, mid-Wales. The results show five salient features. Sodium and chloride concentrations are highly variable and highly correlated in rainfall and mist. The sodium-chloride relationship in rainfall has a slope close to the sodium/chloride ratio in sea-water, and an intercept that is not significantly different from zero. This indicates that sea-salt is the dominant source of both sodium and chloride in rainfall, which would be expected given the maritime nature of the metrology. For mist, there is also a straight line with near-zero intercept, but with a slightly higher gradient than the sea-salt ratio, presumably due to small additional sodium inputs from other sources. There is an approximate input-output balance for both sodium and chloride, with the exception of one groundwater well, in which high chemical weathering results in an anomalous high Na/Cl ratio. Thus, atmospheric deposition is the dominant source of both sodium and chloride in groundwater and streamflow. The fluctuations in sodium and chloride concentrations in the streams and groundwaters are strongly damped compared to those in the rain and the mist, reflecting the storage and mixing of waters in the subsurface. On all timescales, from weeks to years, sodium fluctuations are more strongly damped than chloride fluctuations in streamflow. The additional damping of sodium is consistent with ion exchange buffering of sodium in the catchment soils.  Sodium and chloride concentrations are linearly correlated in the streams and groundwaters, but the slope is almost universally less than the sea-salt ratio and there is a non-zero intercept. The Na/Cl ratio in streamflow and groundwater is higher than the sea-salt ratio when salinity is low and lower than the sea-salt ratio when

  8. Stability of Alprostadil in 0.9% Sodium Chloride Stored in Polyvinyl Chloride Containers.

    Science.gov (United States)

    McCluskey, Susan V; Kirkham, Kylian; Munson, Jessica M

    2017-01-01

    The stability of alprostadil diluted in 0.9% sodium chloride stored in polyvinyl chloride (VIAFLEX) containers at refrigerated temperature, protected from light, is reported. Five solutions of alprostadil 11 mcg/mL were prepared in 250 mL 0.9% sodium chloride polyvinyl chloride (PL146) containers. The final concentration of alcohol was 2%. Samples were stored under refrigeration (2°C to 8°C) with protection from light. Two containers were submitted for potency testing and analyzed in duplicate with the stability-indicating high-performance liquid chromatography assay at specific time points over 14 days. Three containers were submitted for pH and visual testing at specific time points over 14 days. Stability was defined as retention of 90% to 110% of initial alprostadil concentration, with maintenance of the original clear, colorless, and visually particulate-free solution. Study results reported retention of 90% to 110% initial alprostadil concentration at all time points through day 10. One sample exceeded 110% potency at day 14. pH values did not change appreciably over the 14 days. There were no color changes or particle formation detected in the solutions over the study period. This study concluded that during refrigerated, light-protected storage in polyvinyl chloride (VIAFLEX) containers, a commercial alcohol-containing alprostadil formulation diluted to 11 mcg/mL with 0.9% sodium chloride 250 mL was stable for 10 days.

  9. 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.

  10. 21 CFR 172.165 - Quaternary ammonium chloride combination.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Quaternary ammonium chloride combination. 172.165... HUMAN CONSUMPTION Food Preservatives § 172.165 Quaternary ammonium chloride combination. The food additive, quaternary ammonium chloride combination, may be safely used in food in accordance with...

  11. Intrinsic Resistance of Burkholderia cepacia Complex to Benzalkonium Chloride

    OpenAIRE

    Youngbeom Ahn; Jeong Myeong Kim; Ohgew Kweon; Seong-Jae Kim; Jones, Richard C.; Kellie Woodling; Goncalo Gamboa da Costa; LiPuma, John J.; David Hussong; Marasa, Bernard S.; Cerniglia, Carl E.

    2016-01-01

    ABSTRACT Pharmaceutical products that are contaminated with Burkholderia cepacia complex (BCC) bacteria may pose serious consequences to vulnerable patients. Benzyldimethylalkylammonium chloride (BZK) cationic surfactants are extensively used in medical applications and have been implicated in the coselection of antimicrobial resistance. The ability of BCC to degrade BZK, tetradecyldimethylbenzylammonium chloride (C14BDMA-Cl), dodecyldimethylbenzylammonium chloride (C12BDMA-Cl), decyldimethyl...

  12. Retention of vinyl chloride in the human lung.

    OpenAIRE

    Krajewski, J.; Dobecki, M; Gromiec, J

    1980-01-01

    Experiments with volunteers showed that 42% of an inhaled dose of vinyl chloride is retained in the lungs. This value is independent of the concentration of vinyl chloride in the air. Elimination of vinyl chloride through the lungs is negligible since its concentration in expired air decreases immediately after the cessation of exposure.

  13. Kinetics of Vinyl Chloride Polymerization with Mixture of Initiators

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Kinetic models for the rate constants of vinyl chloride polymerization in the presence of initiator mixtures were proposed. They may be used to design the initiator recipes for the vinyl chloride polymerization with uniform rate at different temperatures at which various grades of poly(vinyl chloride) will be prepared.

  14. 46 CFR 154.1740 - Vinyl chloride: Inhibiting and inerting.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Vinyl chloride: Inhibiting and inerting. 154.1740... Operating Requirements § 154.1740 Vinyl chloride: Inhibiting and inerting. When a vessel is carrying vinyl chloride, the master shall ensure that: (a) Section 154.1818 is met; or (b) Section 154.1710 is met,...

  15. A new strategy to stabilize oxytocin in aqueous solutions : I. The effects of divalent metal ions and citrate buffer

    NARCIS (Netherlands)

    Avanti, Christina; Amorij, Jean-Pierre; Setyaningsih, Dewi; Hawe, Andrea; Jiskoot, Wim; Visser, Jan; Kedrov, Alexej; Driessen, Arnold J. M.; Hinrichs, Wouter L. J.; Frijlink, Henderik W.

    2011-01-01

    In the current study, the effect of metal ions in combination with buffers (citrate, acetate, pH 4.5) on the stability of aqueous solutions of oxytocin was investigated. Both monovalent metal ions (Na+and K+) and divalent metal ions (Ca2+, Mg2+, and Zn2+) were tested all as chloride salts. The effec

  16. Mapping the fundamental niches of two freshwater microalgae, Chlorella vulgaris (Trebouxiophyceae) and Peridinium cinctum (Dinophyceae), in 5-dimensional ion space

    Science.gov (United States)

    A five dimensional experimental design, i.e. a five component ion mixture design for nitrate, phosphate, potassium, sodium and chloride projected across a total ion concentration gradient of 1-30 mM was utilized to map the ion-based, scenopoetic, or ‘Grinnellian’, niche space for two freshwater alga...

  17. [Discrimination of plasticizers and screening of phthalates in polyvinyl chloride using DART-TOF/MS].

    Science.gov (United States)

    Abe, Yutaka; Yamaguchi, Miku; Mutsuga, Motoh; Hirahara, Yoshichika; Kawamura, Maiko; Kikura-Hanajiri, Ruri; Goda, Yukihiro; Kawamura, Yoko

    2010-01-01

    A technique using a direct analysis in real time (DART) ion source coupled with time of flight/mass spectrometry (TOF/MS) was developed to discriminate plasticizers and to screen phthalates in polyvinyl chloride (PVC). In DART-TOF/MS analysis of 40 plasticizers, the protonated molecular ion, [M+H](+), was detected for most plasticizers, and the molecular weight could be easily predicted. In the analysis of PVC sheets and toys, mass spectra of plasticizers were successfully detected, and accordingly, plasticizers in PVC were easily discriminated. PVC with a phthalates content in excess of 0.1% could be screened accurately according to the DART-TOF/MS ion intensity of phthalates corresponding to the limit of detection or a suitable criterion value. DART-TOF/MS analysis is a simple and rapid technique that is suitable for the discrimination of plasticizers and for screening of phthalates in PVC.

  18. Iron(III) Chloride mediated reduction of Bis(1-isoquinolylcarbonyl)amide to an Amide

    Indian Academy of Sciences (India)

    Rojalin Sahu; Papuli Chaliha; Vadivelu Manivannan

    2016-01-01

    In methanol, FeCl3 reacted readily with L1H (L1H = bis(1-isoquinolylcarbonyl)amide) and afforded a complex having the formula [Fe(L2)Cl2] (1) {L2− = -((1-isoquinolyl)(methoxy)methyl)isoquinoline-1-carboxamide ion}. This reaction involves reduction of one of the two carbonyl groups present in L1H to (methoxy)methyl group. A plausible mechanism for the conversion of L1H to L2− has been proposed. Determination of molecular structure of 1 confirmed this conversion. Fe(III) ion is surrounded by three nitrogen atoms of the ligand and two chloride ions, imparting a rare distorted trigonal bipyramidal N3Cl2 coordination environment.

  19. Luminescent Properties of Eu3+-Doped Yttrium Oxide Chloride Embedded in Nanoporous Glass

    Institute of Scientific and Technical Information of China (English)

    曾小青; 林凤英; 干福熹; 袁绥华

    2002-01-01

    The photoluminescence of Eu3+-doped yttrium oxide chloride embedded in nanoporous glass has been observed. In comparison with those in the powder phosphor, the emission lines of Eu3+ ions become much broader and blueshift was observed in the lines due to 5D0 → 7F2 transitions and the Eu-O charge transfer excitation band. The ratio intensities of the 5 D0 → 7 F1 transitions to the 5Do → 7 F2 transitions of Eu3+ ion become higher and change at different excitation wavelengths, such as 393nm and 254nm. The two excitation wavelengths belong to the 4f → 4f transition of the Eus+ ion and the Eu-O charge transfer, respectively. This material may be developed into a new luminescent glass.

  20. Controlling the structure and rheology of TEMPO-oxidized cellulose in zinc chloride aqueous suspensions for fabricating advanced nanopaper

    Science.gov (United States)

    Wang, Sha; Zhang, Xin; Hu, Liangbing; Briber, Robert; Wang, Howard; Zhong, Linxin

    Due to its abundance, low-cost, biocompatibility and renewability, cellulose has become an attractive candidate as a functional material for various advanced applications. A key to novel applications is the control of the structure and rheology of suspensions of fibrous cellulose. Among many different approaches of preparing cellulose suspensions, zinc chloride addition to aqueous suspensions is regarded an effective practice. In this study, effects of ZnCl2 concentration on TEMPO-oxidized cellulose (TOC) nanofiber suspensions have been investigated. Highly-transparent cellulose nanofiber suspension can be rapidly obtained by dissolving TOC in 65 wt.% zinc chloride aqueous solutions at room temperature, whereas a transparent zinc ion cross-linked TOC gel could be obtained with zinc chloride concentration as low as 10 wt. %. The structural and rheological characteristics of TOC/ZnCl2 suspensions have been measured to correlate to the performance of thetransparent and flexible nanocellulose paper subsequently produced via vacuum filtration or wet-casting processes.

  1. Growth of L-Valinium Aluminium Chloride single crystal for OLED and super-capacitor applications

    Science.gov (United States)

    Kalaivani, D.; Vijayalakshmi, S.; Theras, J. Elberin Mary; Jayaraman, D.; Joseph, V.

    2015-12-01

    L-Valinium Aluminium Chloride (LVAC), a novel semi-organic material, was grown using slow evaporation under isothermal condition. The single crystal data reveal that the grown crystal belongs to monoclinic system. The SEM micrographs give clear picture about the surface morphology. Further, they confirm the inclusion of aluminium chloride into atomic sites of L-Valine. The compositional elements present in the crystal were identified through EDAX analysis. The mass spectral analysis was carried out to determine the molecular weight of the grown crystal. The optical transparency of the grown crystal was investigated by UV-vis-NIR spectrum. FTIR spectral study was used to identify the functional groups present in the grown material. The luminescence characteristics of grown material were analysed to confirm the effect of metal ion on the ligand. This property makes the material suitable for OLED application. The supercapacitive performance of the grown crystal was finally studied using cyclic voltammetry.

  2. The effect of pulse current on energy saving during Electrochemical Chloride Extraction (ECE) in concrete

    DEFF Research Database (Denmark)

    Sun, Tian R.; Geiker, Mette R.; Ottosen, Lisbeth M.

    2012-01-01

    Energy consumption is a factor influencing the cost of Electrochemical Chloride Extraction (ECE) in concrete. The aims of this work were to investigate the possibility for energy saving when using a pulsed electric field during ECE and the effect of the pulsed current on removal of chloride. Four...... experiments with artificially polluted concrete under same charge transfer were conducted. Results showed that the energy consumption was decreased 15% by pulse current in experiments with 0.2 mA/cm2 current density, which was higher than that of 0.1 mA/cm2 experiments with a decrease of 9.6%. When comparing...... the voltage drop at different parts of the experimental cells, it was found that the voltage drop of the area across the concrete was the major contributor to energy consumption, and results indicated that the pulse current could decrease the voltage drop of this part by re-distribution of ions in pore fluid...

  3. Towards an understanding of solvent extraction--electroanalytical characterization of chloride-leaching solutions.

    Science.gov (United States)

    Paiva, A P; Abrantes, L M

    2001-08-01

    Solvent extraction has been employed to purify media simulating chloride-leaching solutions resulting from complex sulfide concentrate processing, and cyclic voltammetry (CV) has been chosen to characterize those hydrometallurgical aqueous phases. The possibilities of the CV technique were investigated by the evaluation of the adequacy of a specific organic extractant, triisobutylphosphine sulfide, aimed to efficiently and selectively extract silver from a complex chloride medium, additionally containing tenfold to 40-fold molar concentrations of iron, copper and lead. The influence of the oxidation state of the metallic ions present in the feed solution, namely Cu(II) and Cu(I), is considered. The possibilities of CV analysis for the characterization of stripping solutions are also illustrated.

  4. 裂缝对混凝土中氯离子侵蚀作用的影响%lnfluence of cracks on chloride diffusion in concrete

    Institute of Scientific and Technical Information of China (English)

    许兆辉; 刘荣桂; 陆春华; 陈妤; 崔钊玮

    2015-01-01

    为研究裂缝对混凝土中氯离子侵蚀作用的影响,设计了受弯开裂构件,模拟海工环境进行了干湿循环试验,对混凝土构件中氯离子的含量进行测试分析。试验结果表明:构件开裂后氯离子对流扩散区的深度在15~25 mm之间;宏观裂缝加速了氯离子的侵蚀过程,并且以裂缝为新界面,为氯离子的二维扩散提供条件。通过对试验数据总结分析和模拟,基于Fick第二定律提出了综合考虑了时间衰减,裂缝宽度和氯离子结合系数的氯离子扩散模型。%To explore the influence of cracks on chloride diffusion in concrete,a simulated marine environment test is designed,measur-ing the chloride ion content of the pre-cracking components through different wet-dry cycles. The experimental results show that the depth of chlorine ions convection region is 15~25 mm. Macro crack aggravated chloride ions transportation and thereby provided condi-tions for the two-dimensional diffusion of chloride ions based on the cracks as new interface. The chloride diffusion coefficient model is presented considering the time decay,crack width and chloride ion binding coefficient by analyzing and simulating the experimental data.

  5. Relation between chloride exchange diffusion and a conductive chloride pathway across the isolated skin of the toad (Bufo bufo)

    DEFF Research Database (Denmark)

    Kristensen, P; Larsen, Erik Hviid

    1978-01-01

    Substitution of chloride in the outside bathing medium of the toad skin with bromide, iodide, nitrate and sulphate leads to a reduction in the apparent exchange diffusion of chloride across this tissue, and also to a reduction of the chloride current recorded during hyperpolarization. A series of...

  6. Spectroscopic study of the electrochemical behaviour of tantalum(V) chloride and oxochloride species in 1-butyl-1-methylpyrrolidinium chloride

    Energy Technology Data Exchange (ETDEWEB)

    Babushkina, Olga B., E-mail: olga.babushkina@cest.a [Centre in Electrochemical Surface Technology (CEST), Viktor Kaplan street 2, A-2700, Wiener Neustadt (Austria); Ekres, Silvia [Centre in Electrochemical Surface Technology (CEST), Viktor Kaplan street 2, A-2700, Wiener Neustadt (Austria)

    2010-12-30

    FTIR spectroscopy was used to identify the oxochloride species of tantalum(V) in ionic liquids and to confirm the correlations between their presence in electrolytes and the changes in the route of electrochemical reduction of tantalum(V). Electrochemical behaviour of the mixtures (x)1-butyl-1-methyl-pyrrolidinium chloride-(1 - x)TaCl{sub 5} at x = 0.80, 0.65, and 0.40 was investigated over the temperature range 90-160 {sup o}C with respect to the electrochemical deposition of tantalum and was discussed in terms of spectroscopic data. The mechanism of electrochemical reduction of tantalum(V) in the basic and acidic electrolytes depends strongly on the structure and composition of the electro active species of tantalum(V) defined by the molar composition of ionic liquids and on the competition between tantalum(V) chloride and oxochloride species. In the basic mixture at x = 0.80, with octahedral [TaCl{sub 6}]{sup -} ions as the electrochemically active species only the first reduction step Ta{sup 5+} {yields} Ta{sup 4+} at -0.31 V was observed. The competitive reduction of tantalum(V) oxochloride species occurs at more anodic potential (-0.01 V) than the reduction of the chloride complexes and can restrict the further reduction of tantalum(IV). In the basic ionic liquid at x = 0.65, the cyclic voltammograms exhibit reduction peaks at -0.31 V and -0.51 V attributed to the diffusion controlled process as [TaCl{sub 6}]{sup -} + e{sup -} {yields} [TaCl{sub 6}]{sup 2-} and [TaCl{sub 6}]{sup 2-} + e{sup -} {yields} [TaCl{sub 6}]{sup 3-}. The further irreversible reduction of tantalum(III) to metallic state may occur at -2.1 V. In the acidic ionic liquids, at x = 0.40 the electrochemical reduction of two species occurs, TaCl{sub 6}{sup -} and Ta{sub 2}Cl{sub 11}{sup -} and it is limited by two electron transfer for both of them at -0.3 V and -1.5 V, respectively.

  7. Effect of calcium chloride addition on ice cream structure and quality.

    Science.gov (United States)

    Costa, F F; Resende, J V; Abreu, L R; Goff, H D

    2008-06-01

    The influence of calcium fortification by the addition of calcium chloride on quality parameters of ice cream based on physical properties was investigated, as was the effect of kappa-carrageenan at modifying the effects of this calcium fortification. Four ice cream mixes of conventional composition, with added kappa-carrageenan (0 or 0.025%) and added calcium chloride (0 or 4.4 g L(-1) = 40 mM of added Ca(2+)), were prepared. Modulated temperature-differential scanning calorimetry was used to investigate the effect of calcium chloride on the nucleation temperature, enthalpy of melting, and freezing point depression. The protein composition of 15.4% (wt/wt) reconstituted skim milk powder solutions with or without 4.4 g L(-1) added CaCl(2) and in the supernatant after ultracentrifugation was determined. Fat particle size distributions in ice cream were characterized by light scattering. Ice crystal sizes before and after temperature cycling were determined by cold-stage light microscopy. The results demonstrated that the addition of calcium chloride led to a substantial increase in ice crystal sizes and in fat partial coalescence, which were exacerbated by the addition of kappa-carrageenan. These results can be explained by the interaction between Ca(2+) ions and casein micelles, rather than any effects on freezing point depression. The calcium ions led to a more compact micelle, less serum beta-casein, and high fat destabilization, all of which would be expected to reduce macromolecular structure and volume occupancy in the unfrozen phase, which led to increased rates of ice recrystallization.

  8. Performance of fly ash concretes in accelerated and natural chloride exposure regimes

    Energy Technology Data Exchange (ETDEWEB)

    Sorn, V.; Oshiro, T.; Yamada, Y. [Ryukyus Univ., Okinawa (Japan). Dept. of Civil Engineering and Architecture; Sugiyama, T. [Gunma Univ. (Japan). Dept. of Civil Engineering; Matsufuji, Y. [Kyusyu Univ. (Japan). Dept. of Architecture

    2001-07-01

    Serious effort has been made in Japan to make use of the huge quantity of fly ash that is generated each year by coal-based thermal power plants. The produced fly ash contains unburned carbon, rendering it a low quality material classified as Japan Industrial Standard A 6201 class 3. The most efficient use of this kind of fly ash is to use it in concrete, where fly ash is added to the concrete without a corresponding reduction in the quantity of cement. A study was conducted to examine the penetrating characteristics of chloride ions into fly ash concrete and the corrosion of steel reinforcement in concrete, where portions of fine and coarse aggregates were replaced by fly ash. Compressive strength tests were conducted along with chloride penetration tests. Corrosion diagnosis of steel reinforcements was also performed. The physical properties and durability of fly ash concrete against aggressive environments was studied. It was determined that fly ash concretes have higher compressive strength than the control concrete. The strength development of fly ash concrete is very large, particularly on high-volume fly ash concretes. Chloride diffusion coefficients of fly ash concretes derived from the rapid chloride permeability test were found to decrease according to the volume of fly ash added. Chloride penetration of fly ash concretes also decreases with an increase in the volume of fly ash added. Corrosion diagnosis of steel reinforcement in concrete was shown to be effective for evaluating corrosive behaviour of steel reinforcement in fly ash concretes. The values of half-cell potential and polarization resistance measured on fly ash concretes become higher, suggesting no corrosion on steel reinforcement. 6 refs., 4 tabs., 10 figs.

  9. Ion association in natural brines

    Science.gov (United States)

    Truesdell, A.H.; Jones, B.F.

    1969-01-01

    Natural brines, both surface and subsurface, are highly associated aqueous solutions. Ion complexes in brines may be ion pairs in which the cation remains fully hydrated and the bond between the ions is essentially electrostatic, or coordination complexes in which one or more of the hydration water molecules are replaced by covalent bonds to the anion. Except for Cl-, the major simple ions in natural brines form ion pairs; trace and minor metals in brines form mainly coordination complexes. Limitations of the Debye-Hu??ckel relations for activity coefficients and lack of data on definition and stability of all associated species in concentrated solutions tend to produce underestimates of the degree of ion association, except where the brines contain a very high proportion of Cl-. Data and calculations on closed basin brines of highly varied composition have been coupled with electrode measurements of single-ion activities in an attempt to quantify the degree of ion association. Such data emphasize the role of magnesium complexes. Trace metal contents of closed basin brines are related to complexes formed with major anions. Alkaline sulfo- or chlorocarbonate brines (western Great Basin) carry significant trace metal contents apparently as hydroxides or hydroxy polyions. Neutral high chloride brines (Bonneville Basin) are generally deficient in trace metals. With a knowledge of the thermodynamic properties of a natural water, many possible reactions with other phases (solids, gases, other liquids) may be predicted. A knowledge of these reactions is particularly important in the study of natural brines which may be saturated with many solid phases (silicates, carbonates, sulfates, etc.), which may have a high pH and bring about dissolution of other phases (silica, amphoteric hydroxides, CO2, etc.), and which because of their high density may form relatively stable interfaces with dilute waters. ?? 1969.

  10. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Science.gov (United States)

    2010-07-01

    ... Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a polyvinyl chloride plant shall comply with the requirements of this section and § 61.65. (a... is not to exceed 0.02 g vinyl chloride/kg (0.04 lb vinyl chloride/ton) of polyvinyl chloride...

  11. Calcium/thionyl chloride battery technology

    Science.gov (United States)

    Counts, T.

    1985-12-01

    This final report documents the development efforts conducted by the Lithium Batteries Group of the Couples Department of Eagle-Picher Industries. The objective of the project was to develop calcium-thionyl chloride cell technology. The original project was divided into two main tasks. Task One was to consist of component optimization and stability studies. Once sufficiently advanced, the ongoing results of Task One were to be integrated with Task Two. Task Two was to consist of demonstration of an optimized primary cell. In July, 1983, the program was redirected. Task Two was split, with effort to be directed toward both the original primary cell and toward a high discharge rate reserve configuration cell. Additional electrolyte salts were to be evaluated as a means of improving the storability of the active calcium-thionyl chloride cell.

  12. Benzalkonium chloride. Health hazard evaluation report

    Energy Technology Data Exchange (ETDEWEB)

    Bernholc, N.M.

    1984-01-01

    Health hazards associated with the use of benzalkonium chlorides (BAC) are reviewed. Benzalkonium chloride is extensively used as a cationic disinfectant. It is found in a great many over-the-counter and prescription eye products, disinfectants, shampoos, and deodorants, and is used in concentrations that range from 0.001 to 0.01% in eyedrops, up to 2.5% in concentrated liquid disinfectants. Solutions of 0.03 to 0.04% BAC may cause temporary eye irritation in humans but are unlikely to cause any skin response except in persons allergic to quaternary ammonium compounds. Inhalation of a vaporized 10% solution of BAC produced a bronchospasmodic reaction in a previously sensitized individual. At present no other human health effects from BAC have been documented or inferred from exposure to such dilute concentrations.

  13. BARRIER PROPERTIES OF VINYLIDENE CHLORIDE COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    LI Yuesheng; WENG Zhixue; HUANG Zhiming; PAN Zuren

    1996-01-01

    The permeability coefficients of a series of copolymers of vinylidene chloride (VDC)with methyl acrylate (MA), butyl acrylate (BA) or vinyl chloride (VC) (as comonomer)to oxygen and carbon dioxide have been measured at 1.0 MPa and 30℃, while those to water vapor have been measured at 30℃ and 100% relative humidity. All the copolymers are semicrystalline. VDC/MA copolymers have lower melting temperature compared with VDC/BA copolymers, while that melting temperature of VDC/VC copolymer is higher than that of VDC/acrylate copolymers with the same VDC content. The barrier property of the copolymers is predominantly controlled by crystallite, free volume fraction, and cohesive energy. The permeability coefficients of VDC/MA copolymers to oxygen, carbon dioxide, and water vapor were successfully correlated with the ratio of free volume to cohesive energy.

  14. STABILISATION OF SILTY CLAY SOIL USING CHLORIDE

    Directory of Open Access Journals (Sweden)

    TAMADHER T. ABOOD

    2007-04-01

    Full Text Available The object of this paper is to investigate the effect of adding different chloride compounds including (NaCl, MgCl2, CaCl2 on the engineering properties of silty clay soil. Various amounts of salts (2%, 4%, and 8% were added to the soil to study the effect of salts on the compaction characteristics, consistency limits and compressive strength. The main findings of this study were that the increase in the percentage of each of the chloride compounds increased the maximum dry density and decrease the optimum moisture content. The liquid limit, plastic limit and plasticity index decreased with the increase in salt content. The unconfinedcompressive strength increased as the salt content increased.

  15. Iron (III) chloride doping of CVD graphene.

    Science.gov (United States)

    Song, Yi; Fang, Wenjing; Hsu, Allen L; Kong, Jing

    2014-10-03

    Chemical doping has been shown as an effective method of reducing the sheet resistance of graphene. We present the results of our investigations into doping large area chemical vapor deposition graphene using Iron (III) Chloride (FeCl(3)). It is shown that evaporating FeCl(3) can increase the carrier concentration of monolayer graphene to greater than 10(14) cm(-2) and achieve resistances as low as 72 Ω sq(-1). We also evaluate other important properties of the doped graphene such as surface cleanliness, air stability, and solvent stability. Furthermore, we compare FeCl(3) to three other common dopants: Gold (III) Chloride (AuCl(3)), Nitric Acid (HNO(3)), and TFSA ((CF(3)SO(2))(2)NH). We show that compared to these dopants, FeCl(3) can not only achieve better sheet resistance but also has other key advantages including better solvent stability.

  16. The rechargeable aluminum-ion battery

    KAUST Repository

    Jayaprakash, N.

    2011-01-01

    We report a novel aluminium-ion rechargeable battery comprised of an electrolyte containing AlCl3 in the ionic liquid, 1-ethyl-3-methylimidazolium chloride, and a V2O5 nano-wire cathode against an aluminium metal anode. The battery delivered a discharge capacity of 305 mAh g-1 in the first cycle and 273 mAh g-1 after 20 cycles, with very stable electrochemical behaviour. © The Royal Society of Chemistry 2011.

  17. The rechargeable aluminum-ion battery.

    Science.gov (United States)

    Jayaprakash, N; Das, S K; Archer, L A

    2011-12-21

    We report a novel aluminium-ion rechargeable battery comprised of an electrolyte containing AlCl(3) in the ionic liquid, 1-ethyl-3-methylimidazolium chloride, and a V(2)O(5) nano-wire cathode against an aluminium metal anode. The battery delivered a discharge capacity of 305 mAh g(-1) in the first cycle and 273 mAh g(-1) after 20 cycles, with very stable electrochemical behaviour.

  18. The rechargeable aluminum-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Navaneedhakrishnan, Jayaprakash; Das, Shyamal K; Archer, Lynden A.

    2011-01-01

    We report a novel aluminium-ion rechargeable battery comprised of an electrolyte containing AlCl₃ in the ionic liquid, 1-ethyl-3-methylimidazolium chloride, and a V₂O₅ nano-wire cathode against an aluminium metal anode. The battery delivered a discharge capacity of 305 mAh g⁻¹ in the first cycle and 273 mAh g⁻¹ after 20 cycles, with very stable electrochemical behaviour.

  19. Benzalkonium Chloride Intoxication Mimicking Herpes Zoster Encephalitis

    OpenAIRE

    Güler, Ekrem; Olgar, Şeref; Davutoğlu, Mehmet; Garipardıç, Mesut; Karabiber, Hamza

    2011-01-01

    Benzalkonium chloride (BAC) is a frequently used disinfectant and its most well-known side effect is contact dermatitis. In this report, two children who had vesicular dermatitis, headache, lethargy, fever and encephalopathy mimicking Herpes zoster encephalitis were presented. Their consciousness level improved on the second day. From the medical history it was understood that the mother had applied 20% BAC solution to the scalps of two children. The aim of the presentation of this report is ...

  20. Benzalkonium Chloride Intoxication Mimicking Herpes Zoster Encephalitis

    OpenAIRE

    Ekrem Güler; Şeref Olgar; Mehmet Davutoğlu; Mesut Garipardıç; Hamza Karabiber

    2014-01-01

    Benzalkonium chloride (BAC) is a frequently used disinfectant and its most well-known side effect is contact dermatitis. In this report, two children who had vesicular dermatitis, headache, lethargy, fever and encephalopathy mimicking Herpes zoster encephalitis were presented. Their consciousness level improved on the second day. From the medical history it was understood that the mother had applied 20% BAC solution to the scalps of two children. The aim of the presentation of this report is...

  1. EVALUATION OF BACTERICIDAL EFFECTIVENESS OF BENZALKONIUM CHLORIDE

    OpenAIRE

    K. Imandel; M.B. Shaywaard; F. Mobaraki

    1996-01-01

    Benzalkonium chloride is a quaternary ammounium Compounds derivative under different names such as Afxhang, Hamoon, Mahan etc, which have great and expanded use in sanitation and medical affairs. Bactericidal activity of these disinfectants was fulfilled according to National Standard Method No.2842 on Staph. Aureus, Sal. Typhimouium and E. coli. This laboratory test showed that, except Mahan that has not bactericidal efficacy on E.coli at concentration 0.4 percent, other disinfectants under ...

  2. Inactivation of Viruses by Benzalkonium Chloride

    Science.gov (United States)

    Armstrong, J. A.; Froelich, E. J.

    1964-01-01

    Benzalkonium chloride (as Roccal or Zephiran) was found to inactivate influenza, measles, canine distemper, rabies, fowl laryngotracheitis, vaccinia, Semliki Forest, feline pneumonitis, meningopneumonitis, and herpes simplex viruses after 10 min of exposure at 30 C or at room temperature. Poliovirus and encephalomyocarditis virus were not inactivated under the same conditions. It was concluded that all viruses tested were sensitive except members of the picorna group. The literature was reviewed. PMID:4288740

  3. Electrochemical Studies in Aluminum Chloride Melts

    Science.gov (United States)

    1976-07-31

    Molten Salt Systems", Symposium on Molten Salts, Symposium Volume, The Electrochemical Society , in press (1976). Manuscripts in Preparation--Related to...Fused Salt Technology, Electrochemical Society Meeting, Chicaao, May 8-13, 1973. R. A. Osteryoung, R. H. Abel, L. G. Boxall and B. H. Vassos, "An...aluminate Melts", Electrochemical Society , San Francisco, CA, May, 1974. R. A. Osteryoung, "Chemistry in Aluminum Chloride Melts", Fifth International

  4. The Accelerated Test of Chloride Permeability of Concrete

    Institute of Scientific and Technical Information of China (English)

    TAN Ke-feng; ODD E Gjφrv

    2003-01-01

    The availability of accelerated chloride permeability test and the effect of w/c ratio, incorporation of silica fume, maximum aggregate size and aggregate type on the chloride permeability were studied. The mathematic analysis certifies that there is a linear relationship between accelerated test and natural diffusion. Test results show that the chloride permeability of concrete increases as w/c ratio increases whilst a limited amount of replacement of cement with silica fume, the chloride permeability decreases dramatically. The maximum aggregate size in the range of 8 to 25 mm seems also affect chloride permeability but with a much less significant level. The chloride permeability of silica fume lightweight aggregate concrete is very low, especially the concrete made with dry lightweight concrete. The chloride permeability can be evaluated by this accelerated test method.

  5. Potassium chloride production by microcline chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Orosco, Pablo, E-mail: porosco@unsl.edu.ar [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco y Pedernera, San Luis (Argentina); Ruiz, María del Carmen [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina)

    2015-08-10

    Highlights: • Use of chlorination for the KCl production. • The reagents used were microcline, hydromagnesite and chlorine. • Isothermal and non-isothermal assays were performed in Cl{sub 2}–N{sub 2} mixture. • The chlorination generated KCl at 700 °C. • The chlorination products promote KCl formation. - Abstract: The potassium chloride is one of the most important fertilizers used in agriculture. The current demand of this salt makes interesting the study of potassium chloride production from unconventional potassium resources. In this work the potassium chloride production by chlorination of microcline was investigated. The starting reagents were microcline, hydromagnesite and chlorine. Non-isothermal and isothermal chlorination assays were carried out in a thermogravimetric device adapted to work in corrosive atmospheres. The temperature effect on potassium extraction and the phase transformations produced during chlorination of microcline were studied. The reagents and reaction products were analyzed by X-ray fluorescence (XRF) and X-ray diffraction (XRD). The experimental results indicated that by chlorination of microcline an important extraction of potassium in the temperature range from 800 to 900 °C was produced. Moreover, at 800 °C the forsterite, enstatite and magnesium aluminate spinel phases were generated.

  6. Understanding microwave vessel contamination by chloride species.

    Science.gov (United States)

    Recchia, Sandro; Spanu, Davide; Bianchi, Davide; Dossi, Carlo; Pozzi, Andrea; Monticelli, Damiano

    2016-10-01

    Microwaves are widely used to assist digestion, general sample treatment and synthesis. The use of aqua regia is extensively adopted for the closed vessel mineralization of samples prior to trace element detection, leading to the contamination of microwave vessels by chlorine containing species. The latter are entrapped in the polymeric matrix of the vessels, leading to memory effects that are difficult to remove, among which the risk of silver incomplete recoveries by removal of the sparingly soluble chloride is the predominant one. In the present paper, we determined by mass spectrometry that hydrogen chloride is the species entrapped in the polymeric matrix and responsible for vessel contamination. Moreover, several decontamination treatments were considered to assess their efficiency, demonstrating that several cleaning cycles with water, nitric acid or silver nitrate in nitric acid were inefficient in removing chloride contamination (contamination reduction around 90%). Better results (≈95% decrease) were achieved by a single decontamination step in alkaline environment (sodium hydroxide or ammonia). Finally, a thermal treatment in a common laboratory oven (i.e. without vacuum and ventilation) was tested: a one hour heating at 150°C leads to a 98.5% decontamination, a figure higher than the ones obtained by wet treatments which requires comparable time. The latter treatment is a major advancement with respect to existing treatments as it avoids the need of a vacuum oven for at least 17h as presently proposed in the literature.

  7. Lack of the sodium-driven chloride bicarbonate exchanger NCBE impairs visual function in the mouse retina.

    Directory of Open Access Journals (Sweden)

    Gerrit Hilgen

    Full Text Available Regulation of ion and pH homeostasis is essential for normal neuronal function. The sodium-driven chloride bicarbonate exchanger NCBE (Slc4a10, a member of the SLC4 family of bicarbonate transporters, uses the transmembrane gradient of sodium to drive cellular net uptake of bicarbonate and to extrude chloride, thereby modulating both intracellular pH (pH(i and chloride concentration ([Cl(-](i in neurons. Here we show that NCBE is strongly expressed in the retina. As GABA(A receptors conduct both chloride and bicarbonate, we hypothesized that NCBE may be relevant for GABAergic transmission in the retina. Importantly, we found a differential expression of NCBE in bipolar cells: whereas NCBE was expressed on ON and OFF bipolar cell axon terminals, it only localized to dendrites of OFF bipolar cells. On these compartments, NCBE colocalized with the main neuronal chloride extruder KCC2, which renders GABA hyperpolarizing. NCBE was also expressed in starburst amacrine cells, but was absent from neurons known to depolarize in response to GABA, like horizontal cells. Mice lacking NCBE showed decreased visual acuity and contrast sensitivity in behavioral experiments and smaller b-wave amplitudes and longer latencies in electroretinograms. Ganglion cells from NCBE-deficient mice also showed altered temporal response properties. In summary, our data suggest that NCBE may serve to maintain intracellular chloride and bicarbonate concentration in retinal neurons. Consequently, lack of NCBE in the retina may result in changes in pH(i regulation and chloride-dependent inhibition, leading to altered signal transmission and impaired visual function.

  8. Ion channels-related diseases.

    Science.gov (United States)

    Dworakowska, B; Dołowy, K

    2000-01-01

    There are many diseases related to ion channels. Mutations in muscle voltage-gated sodium, potassium, calcium and chloride channels, and acetylcholine-gated channel may lead to such physiological disorders as hyper- and hypokalemic periodic paralysis, myotonias, long QT syndrome, Brugada syndrome, malignant hyperthermia and myasthenia. Neuronal disorders, e.g., epilepsy, episodic ataxia, familial hemiplegic migraine, Lambert-Eaton myasthenic syndrome, Alzheimer's disease, Parkinson's disease, schizophrenia, hyperekplexia may result from dysfunction of voltage-gated sodium, potassium and calcium channels, or acetylcholine- and glycine-gated channels. Some kidney disorders, e.g., Bartter's syndrome, policystic kidney disease and Dent's disease, secretion disorders, e.g., hyperinsulinemic hypoglycemia of infancy and cystic fibrosis, vision disorders, e.g., congenital stationary night blindness and total colour-blindness may also be linked to mutations in ion channels.

  9. Specification of the process of chloride extraction from reinforced concrete based on the inverse task of the diffusion equation

    Directory of Open Access Journals (Sweden)

    Alsabry A.

    2016-05-01

    Full Text Available When the structure of reinforcement is in danger of chloride corrosion it is possible to prevent this disadvantageous phenomenon through exposing the cover to the influence of an electric field. The forces of an electric field considerably reduce chloride ions in pore liquid in concrete, which helps to rebuild a passive layer on the surface of the reinforcement and stops corrosion. The process of removing chlorides can be described with multi-component diffusion equations. However, an essential parameter of these equations, the diffusion coefficient, can be determined on the basis of an inverse task. Since the solution was achieved for one-dimension flow, the method applied can be confirmed by experimental results and the material parameters of the process can be determined theoretically. Some examples of numerical calculations of the effective electro-diffusion coefficient of chloride ions confirmed the usefulness of the theoretical solution for generalizing experimental results. Moreover, the calculation process of the numerical example provides some practical clues for future experimental research, which could be carried out in close connection with the theoretical solution.

  10. Conformation-specific dissociative photoionization of oxalyl chloride in the gas phase

    Science.gov (United States)

    Chu, Genbai; Chen, Jun; Liu, Fuyi; Shan, Xiaobin; Han, Juguang; Sheng, Liusi

    2013-04-01

    The photoionization and photodissociation of oxalyl chloride have been studied by synchrotron vacuum ultraviolet (VUV) photoionization mass spectrometry. The ionization energy of C2Cl2O2 (10.91 ± 0.05 eV) and appearance energies (AEs) for fragment ions CCl2O+, CClO2+, CClO+, CO2+, CO2+, and Cl+ from C2Cl2O2 have been measured from the photoionization efficiency (PIE) spectra. In addition, three conformers of CClO2+ ion, namely trans-, gauche- and cis-conformer are investigated by using CBS-QB3 and W1u methods, which suggest that the existence of the cis-conformation parent ion CClO2+ is consistent with the second onset at 11.6 eV in the experimental PIE curve and the associated calculations. The formation channels of fragment ions near the ionization thresholds are discussed by means of CBS-QB3 and W1u calculated results and thermochemistry results. The dominant fragment ion CClO+ is mainly originated from direct cleavage of the elongated C-C bond in the trans-conformer parent ion after ionization. The calculated results are in good agreement with the experimental data.

  11. Anti-chloride permeability and anti-chloride corrodibility of a green high performance concrete admixture in concrete

    Institute of Scientific and Technical Information of China (English)

    ZHENG Yongbao; LIU Xinrong; LIU Dongyan; CHEN Jiangong; HUANG Xiongjun

    2003-01-01

    The effects of green high performance concrete (GHPC) admixture on the anti-chloride permeability and anti- chloride corrodibility of concrete are studied by a series of experiments designed on the basis of the diffusion principle and electrochemical principle. The GHPC admixture consists of fly ash, gangue, slag, red mud, etc., of which the mass fraction of industrial residues is over 96 %. The anti-permeabilities and anti-corrodibilities of the tested GHPC and normal concrete (NC) are evaluated by the Diffusion Coefficients of chloride which was obtained by measuring the concentration of chloride in the tested systems by the voltage difference method. It is found that the adoption of GHPC admixture greatly improves the anti-chloride permeability and anti-chloride corrodibility by modifying the inner structure and contracting the porosity of concrete to the reduce considerably the diffusion rate of chloride. The admixture is desirable regarding its engineering performances as well as economical and environmental interests.

  12. Environmental and energy gains from using molten magnesium–sodium–potassium chlorides for electro-metallisation of refractory metal oxides

    Directory of Open Access Journals (Sweden)

    Wei Li

    2015-12-01

    Full Text Available The molten eutectic mixture of magnesium, sodium and potassium chlorides (MgCl2–NaCl–KCl has inappreciable solubility for oxide ions, and can help disengage a carbon anode from the oxide ions generated at a metal oxide cathode, and effectively avoid carbon dioxide formation. This “disengaging strategy” was successfully demonstrated in electro-reduction of solid oxides of zirconium and tantalum. It has led to significantly higher current efficiency (93%, and lower energy consumption (1.4 kW h kg−1 in electrolysis of tantalum oxide to tantalum metal compared to the conventional electrolysis in molten calcium chloride (e.g. 78% and 2.4 kW h/kg-Ta.

  13. Cyanide formation by the cyanide distillation of nitrate. Zen shian joryuji ni okeru shosan ion ga kanyosuru shian kagobutsu ion no seisei

    Energy Technology Data Exchange (ETDEWEB)

    Ogura, H. (The Chiba Prefectural Lab. of Water Pollution, Chiba (Japan))

    1994-06-10

    Cyanide ion is formed by reacting disodium ethylenediamine-tetra-acetate (EDTA) with a sample containing nitrous ion. Further, it is known that cyanide ions are also generated from the reaction between EDTA and the product of the reaction of oxide and the substance like hydroxyl ammonium chloride which is added to reduce the oxide contained in the sample. In the present researches, the possibility of the formation of cyanide ions from the nitric acid used popularly in the manufactory of plating and surface-treatment is examined. It is expected that if nitric ion takes a part in the formation of cyanide ion, the reaction reducing the nitric ion into nitrous ion would happen as the former step thereof. Therefore, the cyanide distillation of nitric ions co-existing with the reducing agent is carried out, and it is confirmed that cyanide ion is formed with the participation of EDTA. 14 refs., 1 fig., 7 tabs.

  14. Ion Chromatography.

    Science.gov (United States)

    Mulik, James D.; Sawicki, Eugene

    1979-01-01

    Accurate for the analysis of ions in solution, this form of analysis enables the analyst to directly assay many compounds that previously were difficult or impossible to analyze. The method is a combination of the methodologies of ion exchange, liquid chromatography, and conductimetric determination with eluant suppression. (Author/RE)

  15. Chloride Ingress in Concrete with Different Age at Time of First Chloride Exposure

    DEFF Research Database (Denmark)

    Hansen, Esben Østergaard; Iskau, Martin Riis; Hasholt, Marianne Tange

    2016-01-01

    Concrete structures cast in spring have longer time to hydrate and are therefore denser and more resistant to chloride ingress when first subjected to deicing salts in winter than structures cast in autumn. Consequently, it is expected that a spring casting will have a longer service life....... This hypothesis is investigated in the present study by testing drilled cores from concrete cast in 2012 and 2013 on the Svendborgsund Bridge. The cores are subject to petrographic examination and mapping of chloride profiles. Moreover, chloride migration coefficients have been measured. The study shows...... that the effect of the extra time of hydration obtained when casting in spring increases the expected service life of the concrete structure significantly....

  16. A novel polyvinyl chloride-membrane optical sensor for the determination of Cu2+ ion based on synthesized (N‧1E,N‧2E)-N‧1,N‧2-bis(pyridine-2-ylmethylene)oxalohydrazide: Experimental design and optimization

    Science.gov (United States)

    Ghaedi, M.; Shahamiri, A.; Mirtamizdoust, B.; Hajati, S.; Taghizadeh, F.

    2015-03-01

    A copper (Cu2+) ion-selective bulk optode was constructed by using (N‧1E,N‧2E)-N‧1,N‧2-bis(pyridine-2-ylmethylene)oxalohydrazide as ionophore and NaTPB in DBP matrices. Central composite design under response surface methodology was applied for the optimization of variables including pH, amount of ligand, amount of additive and response time which significantly affect the response of proposed sensor. At optimum specified conditions, the high stability, reproducibility and relatively long lifetime of the optical sensor suggest its ability for accurate and precise monitoring of Cu2+ ion content in various real samples over a concentration range of 1.6 × 10-6 to 3.17 × 10-5 mol L-1 with a limit of detection of 8.1 × 10-7 mol L-1 during response time 6.9 min. The proposed optical sensor was successfully applied for the determination of Cu2+ ion in tap water and different samples.

  17. A novel polyvinyl chloride-membrane optical sensor for the determination of Cu(2+) ion based on synthesized (N'(1)E,N'(2)E)-N'(1),N'(2)-bis(pyridine-2-ylmethylene)oxalohydrazide: experimental design and optimization.

    Science.gov (United States)

    Ghaedi, M; Shahamiri, A; Mirtamizdoust, B; Hajati, S; Taghizadeh, F

    2015-03-01

    A copper (Cu(2+)) ion-selective bulk optode was constructed by using (N'(1)E,N'(2)E)-N'(1),N'(2)-bis(pyridine-2-ylmethylene)oxalohydrazide as ionophore and NaTPB in DBP matrices. Central composite design under response surface methodology was applied for the optimization of variables including pH, amount of ligand, amount of additive and response time which significantly affect the response of proposed sensor. At optimum specified conditions, the high stability, reproducibility and relatively long lifetime of the optical sensor suggest its ability for accurate and precise monitoring of Cu(2+) ion content in various real samples over a concentration range of 1.6×10(-6) to 3.17×10(-5)molL(-1) with a limit of detection of 8.1×10(-7)molL(-1) during response time 6.9min. The proposed optical sensor was successfully applied for the determination of Cu(2+) ion in tap water and different samples.

  18. Isotope separation using high-field asymmetric waveform ion mobility spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Barnett, David A.; Purves, Randy W.; Guevremont, Roger E-mail: roger.guevremont@nrc.ca

    2000-08-01

    A new apparatus for gas-phase separation of stable elemental isotopes at atmospheric pressure is described. A gaseous mixture of chloride isotopes was generated using electrospray ionization and introduced into the analyzer region of a high-field asymmetric waveform ion mobility spectrometer (FAIMS). The ion current exiting the FAIMS was sampled into a quadrupole mass spectrometer for isotope identification.

  19. Study on the mechanism and numerical modeling of chloride ingress in cracked concrete%开裂混凝土内氯离子扩散机理及数值模拟研究

    Institute of Scientific and Technical Information of China (English)

    张红光; 王曙光; 刘伟庆; 徐锋; 刘鑫

    2014-01-01

    The existence of initial damage and cracks provides convenient channels for chloride ions diffusion ,which will further accel-erate the diffusion of chloride ions and further intensify the corrosion deterioration of reinforced concrete.Reviewed previous research ef-forts about chloride ion diffusion problem in cracked concrete,introduced the influences of test methods and parameters of initial cracks on the chloride ion diffusion and concluded the expression of diffusion coefficient for chloride ion in the cracked concrete. Finally numerical simulation was utilized to analyze the whole diffusion process of chloride ions in a concrete immersed into a 100 mol/m 3 chloride solution, and some suggestions for future investigations were made.%初始损伤和裂缝的存在,为氯离子等侵蚀性介质的扩散提供便捷通道,将进一步加速氯离子的扩散,使钢筋混凝土的腐蚀劣化加剧。总结了带裂缝混凝土中氯离子扩散问题的研究成果,重点介绍试验方法以及裂缝参数等因素对氯离子扩散的影响,归纳带裂缝混凝土中氯离子扩散系数的表达式,最后用数值方法模拟混凝土试块在浓度为100 mol/m3的氯化盐溶液中的扩散过程,并为氯离子在开裂混凝土中扩散的研究进行了展望。

  20. On the ion chromatographic determination of S(IV)

    Science.gov (United States)

    Dasgupta, Purnendu K.

    Ion Chromatographie determination of S(IV) is described with special reference to the determination of SO 2(g) and/or aerosol S(IV) along with chloride, nitrate and sulfate in particulate matter. A method is presented for the baseline separation of the above species. The Chromatographic behavior of hydroxymethanesulfonate under various eluent conditions is discussed.