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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

    Energy Technology Data Exchange (ETDEWEB)

    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

    Energy Technology Data Exchange (ETDEWEB)

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

    OpenAIRE

    Gai-Fei Peng; Nai-Qian Feng; Qi-Ming Song

    2014-01-01

    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...

  4. Diffusion behavior of chloride ions in concrete

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, T.; Gjoerv, O.E. [Norwegian Univ. of Science and Technology, Trondheim (Norway). Div. of Building Materials

    1996-06-01

    In the present paper, an analysis of the diffusion behavior of chloride ions in concrete is presented. In concentrated electrolytic aqueous solutions such as seawater or that typically used in laboratory experiments, the effect of ionic interaction may significantly reduce the chemical potential and thus the driving force of the diffusing species. Because of different drift velocities of the cations and chloride ions in the solution, the lagging motion of the cations will also retard the drift velocity of the chlorides. In addition, both the electrical double layer forming on the solid surface and the chemical binding may significantly interfere with the transport of the chloride ions. As a result, the diffusion behavior of the chloride ions in concrete is a more complex and complicated transport process than what can be described by Fick`s law of diffusion.

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

    Directory of Open Access Journals (Sweden)

    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.

  6. Dynamic Electrochemical Measurement of Chloride Ions.

    Science.gov (United States)

    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.

  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. 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)

  9. 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.

  10. 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.

  11. 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.

  12. Computational modelling of chloride ion transport in reinforced concrete

    OpenAIRE

    Meijers, S.J.H.; Bijen, J.M.J.M.; De Borst, R.; Fraaij, A.L.A.

    2001-01-01

    Exposure to a saline environment is a major threat with respect to the durability of reinforced concrete structures. The chloride ions, which are present in seawater and de-icing salts, are able to penetrate the concrete up to the depth of the reinforcement. They can eventually trigger a pitting corrosion process. The assessment of a corrosion-free service life of concrete structures is of paramount economic interest. However, the modelling of the ingress of chloride ions is complicated due t...

  13. Determination of chloride in geological samples by ion chromatography

    Science.gov (United States)

    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.

  14. A chronopotentiometric approach for measuring chloride ion concentration

    NARCIS (Netherlands)

    Abbas, Yawar; Olthuis, Wouter; Berg, van den Albert

    2013-01-01

    In this paper, a novel approach is reported for the electrochemical measurement of chloride ions in aqueous solution. This sensor is based on the stimulus/response principle of chronopotentiometry. A current pulse is applied at the Ag/AgCl working electrode and the potential change is measured with

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

    Science.gov (United States)

    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.

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

    OpenAIRE

    Jae-Im Park; Kwang-Myong Lee; Soon-Oh Kwon; Su-Ho Bae; Sang-Hwa Jung; Sung-Won Yoo

    2016-01-01

    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 concr...

  18. 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.

  19. Electrochemical chloride ion detection technique by using Pt electrode in high temperature water

    International Nuclear Information System (INIS)

    Chloride ion is a representative chemical species causing the corrosion failure of structural materials. For detecting chloride ions in a high temperature solution, the potentio-dynamic polarization and potential transient technique were performed with a Pt electrode. From the polarization behaviour, it was recognized that there is a potential region forming a stable Pt oxide layer to blockade the oxidation reaction of dissolved hydrogen. Since the presence of chloride ions affect the growth of an oxide layer on the metal surface, the potential transient technique was used to investigate the interference of chloride ions for formation of the Pt oxide layer by repeating apply the potential between oxide-free and oxide forming potentials. As a result, the initial oxidation current of dissolved hydrogen appeared to increase with an increase in the chloride ion concentration of the test solutions, and the time for reaching the limiting oxidation current was delayed. From the oxidation current of dissolved hydrogen, we could detect chloride ions down to 2.8 x 10-5 M in high temperature solutions. Consequently, the oxidation current of dissolved hydrogen could be an indicator of chloride ions, because the formation of the Pt oxide layer is sensitively interfered with the chloride ions. (authors)

  20. 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.

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

    Directory of Open Access Journals (Sweden)

    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.

  2. 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.

  3. Influence of chloride ions on actinide chemistry. Effects of radiolysis and temperature

    International Nuclear Information System (INIS)

    This research thesis addresses the chemistry of radionuclides in natural waters, an issue which is related to the management of long life radioactive wastes. Chloride ions are the most concentrated ions but their weak complexing power explains the fact that they are often neglected in speciation calculations. The objective of this research is to identify the influence of chloride ions on transuranium elements (Np, Pu and Am). Their influence is investigated with respect to chemical conditions close to that of underground waters and for concentrated media related to storage conditions in saline media. The author discusses media-related corrections applied to thermodynamic functions, reports a bibliographic study on the stability of actinide chloride complexes, reports a spectrophotometric investigation of complexation by chlorides, and reports the study of the influence of chlorides in a carbonate medium (solubility of americium at different temperatures, and notably at room temperature)

  4. 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.

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

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    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.

  6. Structural Mechanism for Light-driven Transport by a New Type of Chloride Ion Pump, Nonlabens marinus Rhodopsin-3.

    Science.gov (United States)

    Hosaka, Toshiaki; Yoshizawa, Susumu; Nakajima, Yu; Ohsawa, Noboru; Hato, Masakatsu; DeLong, Edward F; Kogure, Kazuhiro; Yokoyama, Shigeyuki; Kimura-Someya, Tomomi; Iwasaki, Wataru; Shirouzu, Mikako

    2016-08-19

    The light-driven inward chloride ion-pumping rhodopsin Nonlabens marinus rhodopsin-3 (NM-R3), from a marine flavobacterium, belongs to a phylogenetic lineage distinct from the halorhodopsins known as archaeal inward chloride ion-pumping rhodopsins. NM-R3 and halorhodopsin have distinct motif sequences that are important for chloride ion binding and transport. In this study, we present the crystal structure of a new type of light-driven chloride ion pump, NM-R3, at 1.58 Å resolution. The structure revealed the chloride ion translocation pathway and showed that a single chloride ion resides near the Schiff base. The overall structure, chloride ion-binding site, and translocation pathway of NM-R3 are different from those of halorhodopsin. Unexpectedly, this NM-R3 structure is similar to the crystal structure of the light-driven outward sodium ion pump, Krokinobacter eikastus rhodopsin 2. Structural and mutational analyses of NM-R3 revealed that most of the important amino acid residues for chloride ion pumping exist in the ion influx region, located on the extracellular side of NM-R3. In contrast, on the opposite side, the cytoplasmic regions of K. eikastus rhodopsin 2 were reportedly important for sodium ion pumping. These results provide new insight into ion selection mechanisms in ion pumping rhodopsins, in which the ion influx regions of both the inward and outward pumps are important for their ion selectivities. PMID:27365396

  7. 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.

  8. 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.

  9. Evaluating capacitive deionization for water desalination by direct determination of chloride ions

    OpenAIRE

    Díaz Baizán, Patricia; González Arias, Zoraida; Granda Ferreira, Marcos; Menéndez López, Rosa María; Santamaría Ramírez, Ricardo; Blanco Rodríguez, Clara

    2014-01-01

    Ionic conductivity and capacitance measurements are widely used methods for evaluating the desalination efficiency in capacity deionization processes. In this study, these methods are revised and several problems associated to them are identified and evaluated. Furthermore, a new method based on the determination of the chloride ion concentration by means of a chloride selective electrode is proposed as a more reliable alternative for evaluating the desalination performance in these systems. ...

  10. 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.

  11. 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

  12. 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.

  13. 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

  14. 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.

  15. 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.

  16. 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.

  17. Durability of sea-sand containing concrete: Effects of chloride ion penetration

    Institute of Scientific and Technical Information of China (English)

    Yin Huiguang; Li Yan; Lv Henglin; Gao Quan

    2011-01-01

    This paper describes an orthogonal experiment on the effect of water/cement ratio, water consumptionper cubic meter, curing time, and type of sand on the response "resistance to chloride ion penetration".A sea-sand containing concrete was used for the trials. An analysis of chloride ion diffusion coefficients at different factor levels was performed. A predictive model of chloride ion diffusion in concrete is developed through regression analysis. The experimental results show that when the water/cement ratio varies from 0.45 to 0.60, and the water consumption per cubic meter varies from 185 to 215 kg. and the curing time varies from 30 to 180 d then the size of the effects fall in the order (most significant first):curing time, type of sand, water consumption per cubic meter, and water/cement ratio. Chloride ion penetration is reduced, and better durability of the concrete is observed, with longer curing times, less water consumption per cubic meter, and a smaller water/cement ratio.

  18. 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

  19. 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...

  20. 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)

  1. Determination of fluoride and chloride content in UO2 powder by selective ion electrode potentiometry method using pyrohydrolitic techniques

    International Nuclear Information System (INIS)

    The flouride and chloride ions in uranium oxide powder should be determined since they influence the performance of fuel element during irradiation in the reactor. Determination of flouride and chloride ion content had been done by selective ion electrode Potentiometry method from uranium oxide after separation from U using method pyrohydrolitic. The experiment showed that the maximum efficiencies of the pyrohydrolitic separation of flouride and chloride ions is 93.78±5.51 % and 95.71±3.08 %, with minimum detection of 0.019 ppm and 1.775 ppm respectively. Uranium matrix as much as 250 ppm showed significant influence on the measurement. (author)

  2. 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.

  3. 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.

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

    Science.gov (United States)

    Armynah, Bidayatul; Halide, Halmar; Zahrawani, Reski, Nurhadi; Tahir, Dahlang

    2016-03-01

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

  5. 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

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

    International Nuclear Information System (INIS)

    The kinetics of the dissolution of stainless steel AISI 430 in the presence of chloride and sulphate ions has been studied in terms of the ion concentration, the pH variation, and the velocity of the working electrode. The experimental method utilized was the potentiostatic anodic polarization, and the reactants used were NaCl and Na2 SO4 at room temperature. Atomic Absorption spectrophotometry and Auger Electrons spectroscopy (AES) analyses were made in order to support the interpretation of results obtained by means of the potentiostatic polarization method. (author)

  7. 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.

  8. 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.

  9. Measurement of chloride-ion concentration with long-period grating technology

    Science.gov (United States)

    Tang, Jaw-Luen; Wang, Jian-Neng

    2007-06-01

    A simple and low-cost long-period fiber grating (LPG) sensor suited for chloride-ion concentration measurement is presented. The LPG sensor is found to be sensitive to the refractive index of the medium around the cladding surface of the sensing grating, thus offering the prospect of development of practical sensors such as an ambient index sensor or a chemical concentration indicator with high stability and reliability. We measured chloride ions in a typical concrete sample immersed in salt water solutions with different weight concentrations ranging from 0% to 25%. Results show that the LPG sensor exhibited a linear decrease in the transmission loss and resonance wavelength shift when the concentration increased. The measurement accuracy for the concentration of salt in water solution is estimated to be 0.6% and the limit of detection for chloride ions is about 0.04%. To further enhance its sensitivity for chloride concentrations, we coated a monolayer of colloidal gold nanoparticles as the active material on the grating surface of the LPG sensor. The operating principle of sensing is based on the sensitivity of localized surface plasmon resonance of self-assembled gold colloids on the grating section of the LPG. With this method, a factor of two increase in the sensitivity of detecting chemical solution concentrations was obtained. The advantages of this type of fiber-optic sensor are that it is compact, relatively simple to construct and easy to use. Moreover, the sensor has the potential capability for on-site, in vivo and remote sensing, and it has potential use as a disposable sensor.

  10. 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

  11. Individual and combined effects of chloride, sulfate, and magnesium ions on hydrated Portland-cement paste

    International Nuclear Information System (INIS)

    Ground water with a high concentration of magnesium ion is known to cause deterioration to portland cement concretes. A proposed mechanism for this deterioration process published previously involves an approximate 1:1 replacement of Ca ions by Mg ions in the crystalline phases of hydrated cement. The current study was undertaken to determine which ions, among magnesium, chloride, and sulfate, cause deterioration; whether their deleterious action is individual or interdependent; and to relate this mechanism of deterioration to the outlook for a 100-yr service life of concretes used in mass placements at the Waste Isolation Pilot Plant. Loss of Ca ion by cement pastes was found to be strongly related to the concentration of Mg ion in simulated ground-water solutions in which the paste samples were aged. This was true of both salt- containing and conventional cement pastes. No other ion in the solutions exerted a strong effect on Ca loss. Ca ion left first from calcium hydroxide in the pastes, depleting all calcium hydroxide by 60 days. Some calcium silicate hydrate remained even after 90 days in the solutions with the highest concentration of Mg ion, while the paste samples deteriorated noticeably. The results indicated a mechanism that involves dissolution of Ca phases and transport of Ca ions to the surface of the sample, followed by formation of Mg-bearing phases at this reaction surface rather than directly by substitution within the microstructure of hydrated cement. Given that calcium hydroxide and calcium silicate hydrate are the principal strength-giving phases of hydrated cement, this mechanism indicates the likelihood of significant loss of integrity of a concrete exposed to Mg-bearing ground water at the WIPP. The rate of deterioration ultimately will depend on Mg-ion concentration, the microstructure materials of the concrete exposed to that groundwater, and the availability of brine

  12. 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.

  13. 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. PMID:27388656

  14. 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.

  15. 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.

  16. 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.

  17. 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%.

  18. Investigation of the pitting of aluminum induced by chloride ions by holographic microphotography

    Directory of Open Access Journals (Sweden)

    LIANG LI

    2008-05-01

    Full Text Available Holographic microphotography was used to investigate the dynamic processes of pitting during anodic dissolution of aluminum in a solution containing chloride ions. The induction and the follow-up propagation processes of the pitting were observed in real-time. A simple model of the propagating process of the pitting was deduced from the result of the holograms of the Al/electrolyte interface. The results prove that holographic microphotography is a useful tool to study the dynamic processes of pitting.

  19. 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.

  20. 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.

  1. One and two dimensional chloride ion diffusion of fly ash concrete under flexural stress

    Institute of Scientific and Technical Information of China (English)

    Yun-sheng ZHANG; Wei SUN; Zhi-yong LIU; Shu-dong CHEN

    2011-01-01

    A preloading frame is firstly designed to accurately apply external flexural stress to concrete specimens.Then a method is developed to measure one and two dimensional (1D and 2D) chloride ion concentrations at different distances from the surface of concrete under flexural stress.Using this method and the preloading frame,1D and 2D stress-diffusion is systematically investigated for fly ash concretes made with different fly ash contents (0%,10%,20%,40%,and 60%),and water to binder ratios (0.3,0.35,and 0.4).The stress accelerating effect on 1D and 2D chloride ion diffusion is also quantitatively analyzed through a comparison between stress-diffusion and nonstress-diffusion.A diffusion accelerating effect caused by external flexural stress can clearly be observed through the comparison.In order to quantify the stress accelerating effect,a stress accelerating factor is proposed in this paper.The relationship between stress accelerating factor and external stress-to-ultimate stress ratio is given as an exponential function.Finally,the process of the initiation,prorogation,and distribution of microcracks on the tensile face of specimen is observed in-situ by using a small-sized loading frame and scanning electron microscope (SEM).The above research provides an insight into chloride attack on the edge reinforcing bars of concrete structures under flexural stress,such as large-span beam and board in the field of civil engineering.

  2. Chloride ion addition for controlling shapes and properties of silver nanorods capped by polyvinyl alcohol synthesized by polyol method

    Science.gov (United States)

    Junaidi, Triyana, Kuwat; Harsojo, Suharyadi, Edi

    2016-04-01

    We report our investigation on the effect of chloride ions oncontrolling the shapes and properties of silver nanorods(AgNRs) synthesized using a polyol method. In this study, we used polyvinyl alcohol (PVA) as a capping agent and sodium chloride (NaCl) as asalt precursor and performed at the oilbath temperature of 140 °C. The chloride ions originating from the NaCl serve to control the growth of the silver nanorods. Furthermore, the synthesized silver nanorodswere characterized using UV-VIS, XRD, SEM and TEM. The results showed that besides being able to control the growth of AgCl atoms, the chloride ions were also able to control the growth of multi-twinned-particles into the single crystalline silver nanorods by micrometer-length. At an appropriate concentration of NaCl, the diameter of silver nanorodsdecreased significantly compared to that of without chloride ion addition. This technique may be useful since a particular diameter of silver nanorods affects a particular application in the future.

  3. Chloride ion addition for controlling shapes and properties of silver nanorods capped by polyvinyl alcohol synthesized using polyol method

    Science.gov (United States)

    Junaidi, Yunus, Muhammad; Triyana, Kuwat; Harsojo, Suharyadi, Edi

    2016-04-01

    We report our investigation on the effect of chloride ions on controlling the shapes and properties of silver nanorods (AgNRs) synthesized using a polyol method. In this study, we used polyvinyl alcohol (PVA) as a capping agent and sodium chloride (NaCl) as a salt precursor and performed at the oil bath temperature of 140°C. The chloride ions originating from the NaCl serve to control the growth of the silver nanorods. Furthermore, the synthesized silver nanorods were characterized using SEM and XRD. The results showed that besides being able to control the growth of AgCl atoms, the chloride ions were also able to control the growth of multi-twinned-particles into the single crystalline of silver nanorods by micrometer-length. At an appropriate concentration of NaCl, the diameter of silver nanorods decreased significantly compared to that of without chloride ion addition. This technique may be useful since a particular diameter of silver nanorods affects a particular application in the future.

  4. Corrosion of alloy 22 in phosphate ions effect and chloride containing solutions

    International Nuclear Information System (INIS)

    Alloy 22 belongs to Ni-Cr-Mo family. This alloy resists the most aggressive environments for industrial applications, in oxidizing as well as reducing conditions, because exhibits an excellent uniform and localized corrosion resistance in aqueous solution. Because of its outstanding corrosion resistant, this alloy is one of the candidate to be considered for the outer shell of the canister that would contain high level radioactive nuclear wastes in a geological repository. The aim of this work is to study ion phosphate influence over Alloy 22 corrosion behavior under aggressive conditions, such as high temperature and high ion chloride concentration, where this material might be susceptible to crevice corrosion. Two different types of samples were used: cylinder specimens for uniform corrosion behavior studies and Prismatic Crevice Assembly (PCA) specimens for localized corrosion studies. Electrochemical tests were performed in deaerated aqueous solution of 1 M NaCl and 1 M NaCl with different phosphate additions at 90 C degrees and pH near neutral. The anodic film and corrosion products obtained were studied by SEM/EDS. Cyclic Potentiodynamic Polarization (CPP) curves obtained for uniform corrosion studies, showed an increase of the passivity range in phosphate containing solutions. The passive current value was 1 μA/cm2 approximately in all the tests. PCA electrochemical tests, that combined a CPP with a potentiostatic polarization step for 2 hours in between the forward and reverse scan, showed crevice corrosion development in some cases. The repassivation potential value, determined by the intersection of the forward and the reverse scan, increased with phosphate addition. A complete crevice corrosion inhibition effect was found for phosphate concentration higher than 0.3 M. These results indicate that the passivity potential range depend on phosphate presence and might be related with the incorporation of the anion in the passive film. Results of the tests

  5. 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.

  6. Determination of the stability constants of lanthanum, praseodymium, europium, erbium and lutetium complexes with chloride ions

    International Nuclear Information System (INIS)

    The stability constants of La3+, Pr3+, Eu3+, Er3+ and Lu3+ 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 (LnCl2+) or two chemical species (LnCl2+ and LnCl2+). The Specific Ion Interaction Theory was applied to the values of log βILn,Cl and the first stability constants at zero ionic strength were calculated by extrapolation. The same theory could not be applied to the log βILn,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 βILn,CI, log βILn,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 βILn,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)

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

    Science.gov (United States)

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

    2010-08-01

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

  8. 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.

  9. 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)

  10. 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

  11. Synergistic effect between cationic gemini surfactant and chloride ion for the corrosion inhibition of steel in sulphuric acid

    Energy Technology Data Exchange (ETDEWEB)

    Qiu Lingguang [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China)], E-mail: lgqiu@ahu.edu.cn; Wu Yun; Wang Yimin; Jiang Xia [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China)

    2008-02-15

    Corrosion inhibition of cold rolled steel in 0.5 mol L{sup -1} sulphuric acid by a quaternary ammonium gemini surfactant, l,3-propane-bis(dimethyl dodecylammonium bromide) (designated as 12-3-12), in the absence and presence of chloride ions was investigated at different temperatures. The results revealed significant synergistic effect between gemini 12-3-12 and chloride ions for the corrosion protection of cold rolled steel in sulphuric acid, and that the novel composite inhibitor system containing cationic gemini surfactant and chloride ions was efficient and low-cost for steel corrosion inhibition in sulphuric acid medium, even when concentration of 12-3-12 was as low as 1 x 10{sup -6} mol L{sup -1}. By fitting the obtained experimental data with Langmuir adsorption model and Arrhenius equation, some thermodynamic and kinetic parameters such as adsorption free energy, the apparent activation energy, and the pre-exponential factor were estimated. The adsorption mechanism of the gemini surfactant onto steel surface in acid medium in the absence and presence of chloride ions was also discussed, respectively.

  12. 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.

  13. 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.

  14. 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)

  15. Electrical characterization of Calcium Aluminate (CA) in presence of chloride ions

    OpenAIRE

    Torres-Luque, Marcela; Osma, Johann F.; Sánchez-Silva, Mauricio; BASTIDAS-ARTEAGA, Emilio; Schoefs, Franck

    2015-01-01

    International audience Chloride ingress is one of the major causes of reinforced concrete degradation. Chlorides accelerate the breaking of the protective layer of rebars favoring pitting corrosion; furthermore, corrosion products generate cracks in concrete, which further accelerate chloride ingress, increase porosity and reduce the strength. From a chemical perspective, the presence of chlorides and its diffusion into the reinforced concrete matrix is highly influenced by the content and...

  16. 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.

  17. Effects of Chloride Ion on the Texture of Copper and Cu-ZrB2 Coatings Electrodeposited from Copper Nitrate Solution in Different Plating Modes

    Institute of Scientific and Technical Information of China (English)

    Dongming GUO; Min ZHANG; Zhuji JIN; Renke KANG

    2006-01-01

    For the first time, the texture of copper and Cu-ZrB2 coatings produced from copper nitrate solution was studied. Chloride ion shows different effects on the deposit texture under direct current(DC)and pulse ion concentration exceeds 20 mg/I. The addition of ZrB2 particles enhances the cathodic polarization of copper deposition, which improves the growth of(111)plane. However, this improvement can be eliminated by further addition of chloride ion.

  18. 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。

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

    OpenAIRE

    Ghahari, S. A.; Ramezanianpour, A. M.; Ramezanianpour, A. A.; Esmaeili, M

    2016-01-01

    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 c...

  20. 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.

  1. 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.

  2. Study by X-ray photoelectron spectroscopy (XPS) and radiochemistry (Cl36) of the interaction of chloride ions with a passive film formed on nickel

    International Nuclear Information System (INIS)

    This research thesis reports the study of the influence of chlorides on nickel passivation by using a radiochemical method based on the use of the Cl36 isotope and the X-ray photoelectron spectroscopy (XPS). The first one allows the in-situ determination of the adsorption of chlorides on the surface, or their inclusion in surface films during the electrochemical treatment. The XPS analysis allows the characterization of modifications induced by chlorides in passive films. The obtained results allow a better understanding in the interpretation of the mechanisms of corrosion induced by chloride ions

  3. Effect of sulfate reducing bacteria on corrosion of stainless steel 1Cr18Ni9Ti in soils containing chloride ions

    International Nuclear Information System (INIS)

    Research highlights: → The effect of SRB on corrosion of the stainless steel was investigated. → The effect of chloride ion on corrosion of the stainless steel was investigated. → Pitting susceptibility of the steel was enhanced by SRB and chloride ion. → Many pitting holes were clearly observed on the surface of the steel. - Abstract: The effect of sulfate reducing bacteria (SRB) on corrosion of stainless steel 1Cr18Ni9Ti in soils containing chloride ions was studied by bacterial analysis, electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM) and energy-dispersive X-ray analysis (EDXA). The results showed that the corrosion rate of the steel in soils containing chloride with SRB was larger than that without SRB under the lower chloride ion concentration of 1 wt%. The observations on pitting corrosion of the steel in soils containing the same amount of SRB, however with different chloride concentration revealed that the pitting depth increased with increasing chloride concentration. There existed in the measured EIS only one capacitive loop for the steel in the soil without SRB, and two capacitive loops for that with SRB.

  4. Separation of chloride and sulfate ions in univalent and divalent cation forms from aqueous streams.

    Science.gov (United States)

    Bader, M S

    2000-04-28

    The precipitation and separation of chloride and sulfate in several cation forms (sodium, potassium, magnesium, calcium, strontium, and barium) from aqueous streams were studied using isopropylamine (IPA) and ethylamine (EA) as precipitation solvents. The precipitation fractions (P) of the tested chloride salts at 5000 and 10,000 ppm by both IPA and EA over the studied range of solvents volume ratio (V(R)) were relatively identical (18-60%) and their small variations were within their experimental uncertainty. The P of combined sulfate at 1000 ppm (56-99.5%) and chloride at 5000 ppm (28-62%) in the form of calcium by IPA over the studied range of V(R) were appreciably higher than the P of sulfate (10-98.5%) from calcium sulfate in the absence of calcium chloride, or the P of chloride (18-58%) from calcium chloride in the absence of calcium sulfate. The P of chloride from oil-field-produced waters at 106,654 ppm (20-88%) by both IPA and EA were higher than the P of chloride from diluted produced water at 20,000 (17-68%) and 10,000 ppm (16-65%) over the studied range of V(R). The small amounts of sulfate present in the produced waters (e.g., 435 ppm) were completely removed at V(R) of 0.1 (the first stage of precipitation). Consistency tests performed on the acquired data indicated a good level of experimental consistency. Two model equations (2-Suffix and 3-Suffix) derived from thermodynamic principles of solid-liquid equilibrium (SLE) criteria were employed to correlate the acquired data. While both equations were adequate for correlating the precipitation data, the 3-Suffix equation was more accurate.

  5. The effect of chloride ion on the iron elution from carbon steel in high temperature water

    International Nuclear Information System (INIS)

    In Hamaoka-5 nuclear power plant, the sea water entered into the reactor during the shutdown on May in 2011. The structural materials were exposed to the high temperature water containing chloride ion (Cl-). Carbon steel is less corrosion-resistant than stainless steel and the corrosion might be accelerated. Oxide growth of carbon steel may cause the change of Co-60 deposition behavior during the operation. Then the perceiving the state of oxide film on the surface of carbon steel is important. We conducted the corrosion tests for 24hrs with carbon steel under high temperature water containing Cl- to estimate the state of the surface and iron elution of the actual plant. In the cases of the prefilmed specimens, without Cl-, the amount of iron elution was small at 513 K. On the other hand, under the water condition containing Cl- iron elution from carbon steel occurred. The iron elution rate under the water condition of 423 K was slightly faster than 513 K. The average values of iron elution rate under the condition of 400ppm as Cl- were approximately 0.03 mg/cm2/h. The dependency of Cl- concentration on iron elution rate did not appear at the both of 423 and 513 K. In the case of the specimens without oxide film, the iron elution rate under the water condition of 423 K was much faster than 513 K under the water conditions with and without Cl-. The iron elution rate of the specimens without oxide film was affected by the concentration of Cl- with the exception of the test at 423 K. At the higher Cl- concentration, iron elution was accelerated. Furthermore, we conducted the corrosion tests at 323 K for 500 hours which simulated the water condition after the shutdown of the reactor. It was also confirmed that iron apparently eluted from the specimen in these tests. This result indicated that iron elution possibly occurred in the actual plant. The analyses of the oxide film on the surface of specimens after the several tests were conducted. We also discussed the

  6. Lithium ions in nanomolar concentration modulate glycine-activated chloride current in rat hippocampal neurons.

    Science.gov (United States)

    Solntseva, E I; Bukanova, J V; Kondratenko, R V; Skrebitsky, V G

    2016-03-01

    Lithium salts are successfully used to treat bipolar disorder. At the same time, according to recent data lithium may be considered as a candidate medication for the treatment of neurodegenerative disorders. The mechanisms of therapeutic action of lithium have not been fully elucidated. In particular, in the literature there are no data on the effect of lithium on the glycine receptors. In the present study we investigated the effect of Li(+) on glycine-activated chloride current (IGly) in rat isolated pyramidal hippocampal neurons using patch-clamp technique. The effects of Li(+) were studied with two glycine concentrations: 100 μM (EC50) and 500 μM (nearly saturating). Li(+) was applied to the cell in two ways: first, by 600 ms co-application with glycine through micropipette (short application), and, second, by addition to an extracellular perfusate for 10 min (longer application). Li(+) was used in the range of concentrations of 1 nM-1 mM. Short application of Li(+) caused two effects: (1) an acceleration of desensitization (a decrease in the time of half-decay, or "τ") of IGly induced by both 100 μM and 500 μM glycine, and (2) a reduction of the peak amplitude of the IGly, induced by 100 μM, but not by 500 μM glycine. Both effects were not voltage-dependent. Dose-response curves for both effects were N-shaped with two maximums at 100 nM and 1 mM of Li(+) and a minimum at 1 μM of Li(+). This complex form of dose-response may indicate that the process activated by high concentrations of lithium inhibits the process that is sensitive to low concentrations of lithium. Longer application of Li(+)caused similar effects, but in this case 1 μM lithium was effective and the dose-effect curves were not N-shaped. The inhibitory effect of lithium ions on glycine-activated current suggests that lithium in low concentrations is able to modulate tonic inhibition in the hippocampus. This important property of lithium should be considered when using this drug as a

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

    OpenAIRE

    D. Thirumalaikumarasamy; K. Shanmugam; Balasubramanian, V

    2014-01-01

    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 uncoate...

  8. Determination of nutrients in the presence of high chloride concentrations by column-switching ion chromatography.

    Science.gov (United States)

    Bruno, P; Caselli, M; de Gennaro, G; De Tommaso, B; Lastella, G; Mastrolitti, S

    2003-06-27

    Determination of inorganic anions in waters of high salinity is one of the most difficult task in analytical chemistry. A simple column-switching method, based on an original chromatographic set-up, for the determination of nutrients (nitrate, nitrite and phosphate) in chloride rich aqueous matrices is presented. A pre-separation system (made of two in line pre-columns, Dionex AG9-HC 4 mm) connected to an analytical column (Dionex AS9-HC 4 mm) by a four way pneumatic valve, allows chloride to be eluted off into the waste and nutrients to be separated and detected by a conductimeter and/or a UV spectrophotometer. Neither chemical pre-treatment nor sample dilution are required; sample matrices presenting a large range of chloride concentrations can be investigated. Moreover by using this technology, automation for routine analysis, low analysis time and low costs can be achieved. LODs of 100, 300, 1000 microg/l for nitrate, nitrite and phosphate, respectively, have been obtained by spiking a synthetic sea water sample containing 20,000 mg/l of chloride and 3000 mg/l of sulphate. Analyte calibration curves of analytes are linear (r>0.99) in the range between the LODs and 60 mg/l. This method was applied to nutrients determination in sea water samples collected near a river outlet. PMID:12899303

  9. 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.

  10. 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.)

  11. Effect of alkali and chloride ions on pitting corrosion behaviour of boron added modified 9Cr-1Mo steel

    International Nuclear Information System (INIS)

    Modified 9Cr-1Mo ferritic steel is used as a structural material for the steam generator of Prototype Fast Breeder Reactor (PFBR) due to its high temperature corrosion and oxidation resistance. Since all the components (tube, tube sheet and shell) of steam generator are made of modified 9Cr-1Mo, it is also required to be resistant against general and localized corrosion. Modified 9Cr-1Mo steel with 100 ppm boron addition is being considered as the structural material for the steam generators of future fast reactors, owing to its improved creep properties. In the present work, an attempt has been made to study the pitting corrosion behaviour of this material in alkaline environment containing chloride ions. Alkaline environment was chosen to simulate the caustic condition generated in the steam generator due to the accidental leak of feed water containing chloride ions (as impurity) with hot sodium. Potentiodynamic anodic polarization studies were carried out in deaerated 0.1, 0.2 and 0.5M sodium hydroxide solutions containing 0.1, 0.2 and 0.5M sodium chloride. During the experiments current value was allowed to increase up to 1 mA to ensure that stable pits were developed. Pitting potentials (Epp) were determined from the anodic polarization diagrams. The pitted specimens etched in Villela's reagent were observed under an optical microscope as well as a scanning electron microscope (SEM). Most of the pits observed under optical microscope were found to be hemispherical in nature. The diameters of 30 random pits were measured (two diameters at right angles for each pit) and an average diameter for each pit was calculated

  12. 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.

  13. Application of sulphoaluminate cement to repair deteriorated concrete members in chloride ion rich environment-A basic experimental investigation of durability properties

    OpenAIRE

    Cai, Gaochuang; Zhao, Jun

    2016-01-01

    This paper presents a basic experimental investigation of the durability properties of Sulphoaluminate cement concrete (SACC) and Portland Cement Concrete (PCC). It is to discuss the potential application of Sulphoaluminate cement towards the repair of deteriorated concrete members in chloride ion-rich environment such as coastal engineering, using a SACC repair layer with higher strength than original damaged concrete. The chloride-related durability properties of SACCs were comprehensively ...

  14. 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%.

  15. 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.

  16. 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.

  17. 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.

  18. Use of Electrochemical Noise (EN) Technique to Study the Effect of sulfate and Chloride Ions on Passivation and Pitting Corrosion Behavior of 316 Stainless Steel

    Science.gov (United States)

    Pujar, M. G.; Anita, T.; Shaikh, H.; Dayal, R. K.; Khatak, H. S.

    2007-08-01

    In the present paper, studies were conducted on AISI Type 316 stainless steel (SS) in deaerated solutions of sodium sulfate as well as sodium chloride to establish the effect of sulfate and chloride ions on the electrochemical corrosion behavior of the material. The experiments were conducted in deaerated solutions of 0.5 M sodium sulfate as well as 0.5 M sodium chloride using electrochemical noise (EN) technique at open circuit potential (OCP) to collect the correlated current and potential signals. Visual records of the current and potential, analysis of data to arrive at the statistical parameters, spectral density estimation using the maximum entropy method (MEM) showed that sulfate ions were incorporated in the passive film to strengthen the same. However, the adsorption of chloride ions resulted in pitting corrosion thereby adversely affecting noise resistance ( R N). Distinct current and potential signals were observed for metastable pitting, stable pitting and passive film build-up. Distinct changes in the values of the statistical parameters like R N and the spectral noise resistance at zero frequency ( R°SN) revealed adsorption and incorporation of sulfate and chloride ions on the passive film/solution interface.

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

    DEFF Research Database (Denmark)

    Christoffersen, Gert Rene Juul; Skibsted, Leif H

    1975-01-01

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

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

    OpenAIRE

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

    2014-01-01

    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 io...

  1. 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.

  2. The electrochemical behaviour study of La3+ ion in fused chlorides bath. The LaNi5 formation

    International Nuclear Information System (INIS)

    The electrochemical behaviour of La3+ ion was studied in fused chlorides bath, with purpose to obtain LaNi5 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 LaCl3 as solute, since 0,25 mol. L-1 up to 2 mol. L-1, between 700 deg C and 800 deg C. The anhydrous LaCl3 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 LaNi5 intermetallic compound was formed with LaCl3 anhydrous concentration of 2 mol. L-1 at 750 deg C, with cathodic current density until 100 mA.cm-2. (author)

  3. About effect of magnesium chloride and some ions in brines on boron coprecipitation by iron hydroxide

    International Nuclear Information System (INIS)

    Studies were made of conditions of precipitation of boron with iron hydroxide from the brines of the mixing zone of the Kara-Bogaz Gol, the mother liquor after the precipitation of potassium salts and artificial manganese chloride solutions at a temperature of 7-45 dee C. The maximum extraction of boron from the brines investigated is observed both in a weakly acid and a weakly alkaline medium. The extraction intensity increases drastically in the range of the maximum with an increase in brine concentration. The anions Cl-, SO42-, and HCO3- present in the brines produce the maximum effect on boron precipitation at a definite pH. This effect depends on the nature of the anions and their ratio in the brine. With a rise in temperature the degree of boron precipitations from the magnesium chloride brine and the precipitate capacity increase as a result of the release of active magnesium hydroxide. When the ratio of Fe2O3 to 100 ml initial solution changes towards increase in precipitating agent at a constant temperature, the precipitate capacity for B2O3 decreases

  4. 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.

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

    OpenAIRE

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

    2007-01-01

    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...

  6. 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.

  7. 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

  8. Chloride ion effect and alloying effect on dealloying-induced formation of nanoporous AuPt alloy

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yan, E-mail: mse_wangy@ujn.edu.cn; Xu, Junling; Wu, Bo

    2013-07-01

    The dealloying of the rapidly solidified Al{sub 66}Au{sub 23.8}Pt{sub 10.2} precursor in the 5 wt.% HCl or 20 wt.% NaOH solution has been investigated using X-ray diffraction, scanning electron microscopy, energy dispersive X-ray analysis and transmission electron microscopy, in order to clarify the chloride ion effect and alloying effect on the formation of nanoporous Au–Pt alloy. The Al{sub 66}Au{sub 23.8}Pt{sub 10.2} precursor is composed of a single Al{sub 2}Au-type intermetallic compound and only Au(Pt) solid solution can be identified in the as-dealloyed sample. The Pt addition can significantly refine the nanoporous structure during the dealloying of the Al{sub 66}Au{sub 23.8}Pt{sub 10.2} precursor either in the HCl or NaOH solution. Moreover, the alloying effect of Pt markedly exceeds the coarsening effect of chloride ion adsorption for the formation of nanoporous Au–Pt. The average ligament size is 5.2 ± 0.7 and 3.3 ± 0.4 nm for the nanoporous Au–Pt alloy obtained in the HCl and NaOH solution, respectively. In addition, electrochemical measurements including potentiodynamic polarization and cyclic voltammetry have also been performed on the Al{sub 66}Au{sub 23.8}Pt{sub 10.2} precursor.

  9. 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.

  10. Donnan effect on chloride ion distribution as a determinant of body fluid composition that allows action potentials to spread via fast sodium channels

    Directory of Open Access Journals (Sweden)

    Kurbel Sven

    2011-05-01

    Full Text Available Abstract Proteins in any solution with a pH value that differs from their isoelectric point exert both an electric Donnan effect (DE and colloid osmotic pressure. While the former alters the distribution of ions, the latter forces water diffusion. In cells with highly Cl--permeable membranes, the resting potential is more dependent on the cytoplasmic pH value, which alters the Donnan effect of cell proteins, than on the current action of Na/K pumps. Any weak (positive or negative electric disturbances of their resting potential are quickly corrected by chloride shifts. In many excitable cells, the spreading of action potentials is mediated through fast, voltage-gated sodium channels. Tissue cells share similar concentrations of cytoplasmic proteins and almost the same exposure to the interstitial fluid (IF chloride concentration. The consequence is that similar intra- and extra-cellular chloride concentrations make these cells share the same Nernst value for Cl-. Further extrapolation indicates that cells with the same chloride Nernst value and high chloride permeability should have similar resting membrane potentials, more negative than -80 mV. Fast sodium channels require potassium levels >20 times higher inside the cell than around it, while the concentration of Cl- ions needs to be >20 times higher outside the cell. When osmotic forces, electroneutrality and other ions are all taken into account, the overall osmolarity needs to be near 280 to 300 mosm/L to reach the required resting potential in excitable cells. High plasma protein concentrations keep the IF chloride concentration stable, which is important in keeping the resting membrane potential similar in all chloride-permeable cells. Probable consequences of this concept for neuron excitability, erythrocyte membrane permeability and several features of circulation design are briefly discussed.

  11. Effect of the chloride ions on the hydrolysis of praseodymium in a 2M ion force media

    International Nuclear Information System (INIS)

    The constants of the product of solubility and the first of hydrolysis were determined of the Praseodymium in media 2M of NaClO4 and 2M of NaCl, to 303 K and under conditions free of CO2. The diagram of solubility was obtained (pPr(ac) - pCH), by means of a radiochemical method and with it was established the pCH 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 βPr,Cl of the specie PrCI2+ starting from the hydrolysis constants obtained in the perchlorate and chloride media. (Author)

  12. 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...

  13. 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.

  14. 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%.

  15. Determination of fluoride and chloride in nickel ore by ion chromatography%离子色谱法测定镍矿中氟和氯

    Institute of Scientific and Technical Information of China (English)

    窦怀智; 陆彩霞; 侯晋

    2012-01-01

    The simultaneous determination of fluoride and chloride contents in nickel ore by ion chromatography was established. The sample was decomposed by H2SO4. After water steam distillation at 160-180℃, the fluoride and chloride in testing solution would be released and absorbed by NaOH so-lution, realizing the separation from matrix and other elements. Then, the contents of fluoride and chloride were determined by ion chromatography. The high-capacity IonPac? AS23 anion separation column (4 mm×250 mm) and IonPac? AG23 protection column (4 mm×50 mm) were used as chro-matographic column and 20 mmol/L NaOH solution was used as eluent. Fluoride and chloride were detected with conductivity detector. The results showed that the peak area of fluoride and chloride had good linear relationship with their contents in the range of 1-25 μg/mL. The correlation coefficients ? were 1. 000 0 and 0. 999 6 for fluoride and chloride respectively. The determination results of fluoride and chloride in sample showed high precision. The recoveries of standard addition were all greater than 95%.%建立了同时测定镍矿中氟、氯含量的离子色谱法.试样经硫酸分解后,在160~180℃的温度下进行水蒸气蒸馏,试液中的氟和氯随着水蒸气逸出并被NaOH吸收液吸收,与基体和其他元素分离,吸收液中的氟和氯用离子色谱法测定.以高容量IonPac(R) AS23型阴离子分离柱(4 mm×250 mm)和IonPac(R) AG23型保护柱(4mm×50 mm)为色谱柱,20 mmol/LNaOH溶液为淋洗液,用电导检测器检测.结果表明,氟和氯含量在1~25μg/mL范围内与相应的峰面积呈良好的线性关系,相关系数(R)分别为1.000 0和0.999 6,样品中氟、氯测定结果具有较高精密度,加标回收率均达到95%以上.

  16. The corrosive influence of chloride ions preference adsorption on α-Al2O3 (0 0 0 1) surface

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • The preference adsorption and interaction of Cl− at increasing monolayer coverage on Al2O3 in solution environment are modeling by DFT with COSMO. • A redefinition critical one plane monolayer of Cl− is 3/7, and the adsorption energy decrease in three steps, each adsorption energy step only relate to the adsorption site and the morphology. • The weaker interaction between Cl− and Al2O3 surface but stronger interactions between three Cl− make the electrons uniformly occupy on the energy levels of three ions. - Abstract: Conductor-like screening model (COSMO), Periodic DFT calculations have been performed on a Al2O3 surface to model the influence of preference adsorption and interaction of chloride ions at increasing monolayer coverage on undefective passive film on Aluminum in solution environment. The results evidence that the critical monolayer of Cl− is 3/7, which is redefined. With increasing Cl− adsorption, both the first and second Cl− move from Al(1) atop and bridge10 sites to O(5) sites, suggesting that the weaker interaction between Cl− and Al2O3 surface but stronger interactions between three ions make the electrons uniformly occupy on the energy levels of them. More calculations shows that the preference adsorption sites of Cl− are independent of the surface area of oxide, and the adsorption energy decrease in three steps, each adsorption energy step only relate to the adsorption site and the morphology. On undefective oxide film, low coverage Cl− adsorption would restrain surface breakdown to happen which is consistent with the experiment results

  17. Increasing Ubiquitin Ion Resistance to Unfolding in the Gas Phase Using Chloride Adduction: Preserving More "Native-Like" Conformations Despite Collisional Activation.

    Science.gov (United States)

    Wagner, Nicole D; Kim, Doyong; Russell, David H

    2016-06-01

    Electrospray ionization (ESI) of ubiquitin from acidified (0.1%) aqueous solution produces abundant ubiquitin-chloride adduct ions, [M + nH + xCl]((n - x)+), that upon mild heating react via elimination of neutral HCl. Ion mobility collision cross section (CCS) measurements show that ubiquitin ions retaining chloride adducts exhibit CCS values similar to those of the "native-state" of the protein. Coupled with results from recent molecular dynamics (MD) simulations for the evolution of a salt-containing electrospray droplet, this study provides a more complete picture for how the presence of salts affects the evolution of protein conformers in the final stages of dehydration of the ESI process and within the instrument. PMID:27137645

  18. 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.

  19. The role of Mg2+ ions in the corrosion behaviour of AA2024-T3 aluminium alloys immersed in chloride-containing environments

    International Nuclear Information System (INIS)

    It is well-known the harmful impact of chloride ions in the corrosion behaviour of aluminium and its alloys. The present work investigates the use of Mg2+ ions as corrosion inhibitors of AA2024-T3 samples immersed in chloride-containing electrolytes. AA2024-T3 samples were immersed into an electrolyte containing chloride ions, in absence or presence of Mg2+. The electrochemical behaviour was studied by potentiondynamic polarization and electrochemical impedance spectroscopy techniques. The results showed the beneficial effects afforded by the Mg2+ ions. First, the open circuit potential was shifted towards more cathodic values and, on the other hand, the impedance values obtained for samples tested in presence of Mg2+ were higher, suggesting a slowdown of the corrosion rate. The morphological characterization was performed using scanning electron microscopy and energy dispersive X-ray spectroscopy. The results demonstrated that the presence Mg2+ hinders Mg dealloying of the S phase particles, which delays their change from anodic to cathodic behaviour, so delaying the subsequent Al matrix galvanic attack. An additional protection mechanism is related to the blockage of cathodic areas by the precipitation of Mg(OH)2 in alkaline environments

  20. 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.

  1. 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)

  2. 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. PMID:26942523

  3. 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.

  4. Photochemical transformation of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) in surface coastal waters: Effects of chloride and ferric ions

    International Nuclear Information System (INIS)

    Highlights: • Chloride ion promoted the phototransformation of BDE-47 in Fe(III) solution. • In Fe(III) solution, the added Cl− could influence the generation of ·OH. • The chlorinated PBDEs were found in Fe(III) + Cl− solution under irradiation. • These results showed the likely fate of PBDEs in the marine environment. - Abstract: The effects of several aquatic environmental factors on the photochemical transformation of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) have been investigated. Ferric ion (Fe(III)) has been found to promote the phototransformation of BDE-47, and this process is further enhanced with the added chloride ion (Cl−), while it is suppressed with increasing pH. Electron spin resonance results show that the formation of hydroxyl radical, and the added Cl− could influence the generation of hydroxyl radical in Fe(III) solution. Hence, Cl− enhances the phototransformation of BDE-47 most probably because of the reaction with Fe(III) species under irradiation, yielding hydroxyl and chloride radicals. These radicals can not only decompose PBDEs, but also lead to their photodebromination and photochlorination. These results indicate that the aquatic environmental factors and Cl− in particular played an important role in the photochemical transformation process of PBDEs, providing insight into the likely fate of PBDEs in the marine environment

  5. 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.

  6. Effect of Chloride Ions on Thaumasite Formation%氯离子对碳硫硅钙石形成的影响

    Institute of Scientific and Technical Information of China (English)

    李长成; 姚燕; 王玲

    2011-01-01

    A thaumasite form of sulfate attack accelerated test was carried out to investigate the effect of chloride ions on thaumasite formation. Cement-limestone powder paste samples were immerged in NaCl/Na2SO4 composite solution at different concentrations.The appearance of corroded samples was observed. Besides, the corrosion products were also analyzed by X-ray diffraction and inflared spectrum methods. The results show that the sample immerged in pure Na2SO4 solution occurs serious thaumasite form of sulfate attack after 12 months immersion, and the corrosion products are mainly thaumasite and gypsum. The damage got more and more serious, and the sample finally became a no-cementitious mud-like material from the outside to the inside with time. However, the corrosion degree of samples and thaumasite content of corrosion products both decreased with increasing the chloride ions concentration of NaCl/Na2SO4 composite solution. Chloride ions can slow thaumasite formation speed, and the higher the concentration of chloride ions is, the slower the effect of chloride ions on thaumasite formation.%研究了氯离子对碳硫硅钙石形成的影响,将水泥-石灰石粉净浆样品浸泡在(5±2)℃不同质量分数的NaCl/Na2SO4复合溶液中,观察侵蚀后样品的外观,并对腐蚀产物进行x射线衍射、红外光谱分析.结果表明:纯Na2SO4溶液中的样品发生碳硫硅钙石型硫酸盐侵蚀,腐蚀产物以碳硫硅钙石及石膏为主,随着时间的延长而日益严重,由表及里逐渐变为一种无胶凝性的烂泥状物质.NaCl/Na2SO4复合溶液中样品的硫酸盐侵蚀程度和腐蚀产物中碳硫硅钙石量随氯离子浓度的提高而逐渐降低.氯离子减缓了碳硫硅钙石的形成速度,并且氯离子浓度越高减缓效果越显著.

  7. 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.

  8. Electrochemical oxidation of acid black 210 dye on the boron-doped diamond electrode in the presence of phosphate ions: Effect of current density, pH, and chloride ions

    International Nuclear Information System (INIS)

    The electrochemical oxidation of acid black 210 dye (AB-210) on the boron-doped diamond (BDD) was investigated under different pH conditions. The best performance for the AB-210 oxidation occurred in alkaline phosphate solution. This is probably due to oxidizing agents such as phosphate radicals and peroxodiphosphate ions, which can be electrochemically produced with good yields on the BDD anode, mainly in alkaline solution. Under this condition, the COD (chemical oxygen demand) removal was higher than that obtained from the model proposed by Comninellis. Electrolyses performed in phosphate buffer and in the presence of chloride ions resulted in faster COD and color removals in acid and neutral solutions, but in alkaline phosphate solution, a better performance in terms of TOC removal was obtained in the absence of chloride. Moreover, organochloride compounds were detected in all electrolyses performed in the presence of chloride. The AB-210 electrooxidation on BDD using phosphate as supporting electrolyte proved to be interesting since oxidizing species generated from phosphate ions were able to completely degrade the dye without producing organochloride compounds.

  9. 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.

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

    International Nuclear Information System (INIS)

    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 (Kd) 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 Qmax 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.

  11. 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.

  12. 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.

  13. Chloride binding of cement-based materials subjected to external chloride environment - A review

    OpenAIRE

    Yuan, Q.; Shi, C; Schutter, G. de; Audenaert, K.; Deng, D.

    2009-01-01

    This paper reviews the chloride binding of cement-based materials subjected to external chloride environments. Chloride ion exist either in the pore solution, chemically bound to the hydration products, or physically held to the surface of the hydration products. Chloride binding of cement-based material is very complicated and influenced by many factors, such as chloride concentration, cement composition, hydroxyl concentration, cation of chloride salt, temperature, supplementary cementing m...

  14. 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

  15. 有机肥料中氯离子检测方法的研究%Study on detection method of chloride ion in organic fertilizers

    Institute of Scientific and Technical Information of China (English)

    杜颖; 刘善江; 陈益山

    2015-01-01

    通过全自动电位滴定法与佛尔哈德法对有机肥料样品中氯离子含量进行测定比较,结果显示,自动电位滴定法不受溶液颜色干扰,测定更为快速、准确,平均回收率为97.1%。此种方法缩短了前处理时间,使实验操作更为便捷。同时该法适用于植株中的氯离子含量的测定。%The chloride ion content in organic fertilizer samples were determined using both automatic potentiometric titration and Volhard method and they were compared in this study. The results showed that the automatic potentiometric titration was not influenced by solution color it was more rapidly and accurately than Volhard method, and the average recovery rate was 97. 1%. This method could shorten the pretreatment time, make the operation more convenient. By the way, this method could be suitable for the determination of chloride ion content in plants.

  16. 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。

  17. 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 ...

  18. 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.

  19. Formation of La3+, Pr3+, Eu3+, Er3+, and Lu3+ complexes with chloride ions, in aqueous medium

    International Nuclear Information System (INIS)

    The constants of stability of the complexes of La3+, Pr3+, Eu3+, Er3+, and Lu3+ with Cl- ions, its were determined, in the aqueous medium of HCI - HClO4 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 LnCI2+ species diminishes when increasing the ion force and the charge density. (Author)

  20. 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...

  1. 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.

  2. 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.

  3. 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.

  4. 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。

  5. 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.

  6. 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.

  7. 环境条件和应力水平对混凝土中氯离子传输的影响%Effects of environmental conditions and stress level on chloride ion transport in concrete

    Institute of Scientific and Technical Information of China (English)

    张伟平; 张庆章; 顾祥林; 钟丽娟; 黄庆华

    2013-01-01

    To investigate the diffusion process of chloride ion in concrete under atmosphere environment, a series of tests were conducted under the conditions of different salt-fog spray angle, environment temperature, mass concentration of sodium chloride solution and compressive stress level. The results show that surface chloride ion mass fraction for specimens under different spray angles of salt-fog were different, which leads to a great change of diffusion degree of chloride ions in concrete. The surface chloride ion mass fraction is high when the angle of erosion surface is 0° or 45°, which causes severe erosion in concrete. The surface chloride ion mass fraction is increased with the increasing of mass concentration of sodium chloride solution until a stable value. The apparent diffusion coefficient of chloride ion is increased with the increasing of temperature, and decreased significantly with the increasing of compressive stress level due to the dense concrete by stress.%为了研究自然环境中混凝土的氯盐侵蚀过程,进行了不同侵蚀角度、氯化钠溶液质量浓度、环境温度、应力水平下的混凝土盐雾加速侵蚀试验,分别探讨了在不同的条件下氯离子在混凝土中的扩散规律.结果表明:盐雾箱中试件放置角度不同,其表面氯离子聚集量会不同,最终导致氯离子侵蚀程度不同,其中以平面或45°侧面为侵蚀面时,表面氯离子质量分数较高,氯离子侵蚀程度严重;随着氯化钠溶液质量浓度的增大,盐雾沉降量增加,表面氯离子质量分数也增加,不过最终会达到一个衡定值;随着环境温度的升高,氯离子表观扩散系数逐渐增大;由于压应力状态下混凝土内部结构更加密实,氯离子表现扩散系数显著减小.

  8. Zirconium ion selective electrode based on bis(diphenylphosphino) ferrocene incorporated in a poly(vinyl chloride) matrix

    Energy Technology Data Exchange (ETDEWEB)

    Gholivand, M.B. [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of)]. E-mail: mbgholivand@yahoo.com; Babakhanian, A. [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Joshaghani, M. [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of)

    2007-02-19

    A novel potentiometric zirconium - PVC matrix membrane sensor incorporating bis(diphenylphosphino) ferrocene as an electroactive material and tris(2-ethylhexyl)phosphate as solvent mediator is described. In mixed acetate buffer solution of pH 4.8, the sensor displays a rapid and linear response for zirconium ion over the concentration range 1.0 x 10{sup -1} to 1.0 x 10{sup -7} mol L{sup -1} with a good slope of 59.7 {+-} 0.3 mV per decade and detection limit 1.8 x 10{sup -8} mol L{sup -1}. The best performance was obtained with membrane composition 33% PVC, 65% TEHP, 1% NaTPB and 1% ionophore. The proposed electrode revealed excellent selectivity for zirconium ion over a wide variety of alkali, alkaline earth, transition and heavy metal ions and could be used in a pH range of 4.15-7.8. The electrode was applied for at least 1 month without any considerable divergence in the potential responses. The practical utility of the electrode has been demonstrated by its use as an indicator electrode in the potentiometric titration of zirconium ions with sodium fluoride and in determination of zirconium ion in some alloy, tape and waste water samples.

  9. 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.…

  10. Naked eye sensor on polyvinyl chloride platform of chromo-ionophore molecular assemblies: A smart way for the colorimetric sensing of toxic metal ions

    International Nuclear Information System (INIS)

    We demonstrate the possibility of fabricating a simple, naked eye colorimetric sensor miniature, using chromo-ionophore molecular assemblies anchored on polyvinyl chloride (PVC) surface. The ion-sensing probe (4-n-dodecyl-6-(2-thiazolylazo)-resorcinol) provides a better efficiency with PVC platform in developing a series of colour transitions, while targeting trace levels of Cd2+, Pb2+ and Hg2+. The physical properties of the film sensor are controlled by measuring the probe isotherm plot. The surface morphology and molecular composition of the solid-state optical sensor are characterized using X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The changes in sensor's optical intensity and its response time for the target analytes are followed by absorption spectroscopy. High speed of response (t ≤ 5 min) and confidence in determination of analytes from chemically complex matrices has been achieved, using simulated synthetic mixtures and spiked real environmental samples, with a relative standard deviation of 2+, Pb2+ and Hg2+ ions, respectively. The sensor strips are reversible and reusable without any change in the sensing efficiency, up to four cycles. The signal response observed with the proposed method is consistent between sensors, and also are stable over time

  11. Photoelectrocatalytic decontamination of oilfield produced wastewater containing refractory organic pollutants in the presence of high concentration of chloride ions.

    Science.gov (United States)

    Li, Guiying; An, Taicheng; Chen, Jiaxin; Sheng, Guoying; Fu, Jiamo; Chen, Fanzhong; Zhang, Shanqing; Zhao, Huijun

    2006-11-16

    The feasibility study of the application of the photoelectrocatalytic decontamination of high saline produced water containing refractory organic pollutants was investigated in the slurry photoelectrocatalytic reactor with nanometer TiO2 particle prepared with sol-gel method using the acetic acid as hydrolytic catalyst. The efficiency of the photoelectrocatalytic decontamination of produced water was determined with both COD removal from the tested wastewater and the decrease of mutagenic activity evaluated by Ames tests. The experimental results showed that the photoelectrocatalysis is a quite efficient process for decontaminating the produced water, although there are high concentration of salt existed in oilfield wastewater. We found that the COD removal efficiencies by photoelectrocatalytic process are much higher than that of by photocatalytic or electrochemical oxidation individually in the photoelectrocatalytic reactor. The COD removal can be substantially improved by the added H2O2 and the generation of active chlorine from high concentration chlorides in the wastewater. The effects of various operating conditions, such as initial COD concentration, applied cell voltage, catalyst amount and initial pH value of solution, on the photoelectrocatalytic efficiencies, is also investigated in detail. The results showed that when the raw produced wastewater was diluted in a 1:1 (v/v) ratio, there is a highest COD removal efficiency. And the photoelectrocatalytic degradation of organic pollutants in saline water is much favored in acidic solution than that in neutral and/or alkaline solution. PMID:16875777

  12. Comment on ''Mean force potential for the calcium--chloride ion pair in water'' [J. Chem. Phys. 99, 4229 (1993)

    International Nuclear Information System (INIS)

    The interionic potential of mean force (pmf) for the Ca++--Cl- ion pair in water is computed using the molecular dynamics computer simulation technique. The calculated pmf indicates a stable contact pair (CIP) and a solvent-separated pair (SSIP) centered at 2.9 and 5.0 A with a 2.8 kcal/mol barrier to dissociation. The SSIP well is about 2.0 kcal/mol deeper than the CIP suggesting that water molecules in the first hydration shell are strongly coordinated to the Ca++ ion. Our results do not agree with the pmf reported recently by Guardia, Robinson, Padro [J. Chem. Phys. 99, 4229 (1993)]. Possible reasons for the discrepancy are discussed

  13. A Hydrogen Ion-Selective Poly(Vinyl Chloride) Membrane Electrode Based on Calix[4]arene as a Perchlorate Ion-Selective Electrode

    OpenAIRE

    CANEL, Esin; ERDEN, Sevcan; ÖZEL, Ayça DEMİREL; MEMON, Sahahabuddin

    2008-01-01

    A hydrogen ion-selective electrode was prepared using 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetracyanometoxy-calix[4]arene and the possibility of its use as a perchlorate ion-selective electrode was investigated using its characteristic of becoming perchlorate sensitive in acidic regions. The electrode of the optimum characteristic had a composition of 1% ionophore, 66% o-NPOE, and 33% PVC. This electrode exhibited a linear response over the range 1.0 \\times 10-1-1.0 \\times 10-5 M o...

  14. Analysis of sugars and sugar polyols in atmospheric aerosols by chloride attachment in liquid chromatography/negative ion electrospray mass spectrometry.

    Science.gov (United States)

    Wan, Eric C H; Yu, Jian Zhen

    2007-04-01

    Sugars and sugar polyols are relatively abundant groups of water-soluble constituents in atmospheric aerosols. This paper describes a method that uses liquid chromatography-mass spectrometry (LC-MS) to analyze sugars and sugar polyols in atmospheric aerosols, ranging from C3 sugar alcohols to trisaccharides. Postcolumn addition of chloroform in acetonitrile was found to greatly enhance ionization of these compounds by forming chloride adduct ions in the negative-ion mode using electrospray ionization. A gradient elution program starting at 5%:95% H20/acetonitrile and ending at 30%:70% H2O/acetonitrile provides baseline separations of the sugars and sugar polyols on an amino-based carbohydrate column. The detection limits based on quantification of [M + 35Cl]- adduct ions were in the order of 0.1 microM. By eliminating the need for derivatization, this LC-MS based method provides a simpler alternative method to the commonly used and more laborious gas-chromatography based methods. It also has an additional advantage of being able to quantify trisaccharide sugars. The method was applied to analyze 30 ambient samples of fine particulate matter collected at a site away from urban centers in Hong Kong. The sugar compounds positively identified and detected in the ambient samples included four sugar alcohols (glycerol, erythritol, xylitol, and mannitol), three monosacchride sugars (xylose, fructose, and glucose), two disaccharides (sucrose, trehalose), two trisaccharides (melezitose, raffinose), and one anhydrosugar (levoglucosan). The sum of these sugar and sugar polyol compounds ranged from 38 to 1316 ng m(-3), accounting for an average of 1.3% organic carbon mass. Through the use of a principal component analysis of the ambient measurements, the mono- to trisactharide sugars and C3-C5 sugar polyols were identified to be mainly associated with soil/soil microbiota while the anhydrosugar (levoglucosan) was associated with biomass burning. PMID:17438800

  15. Simultaneous determination of trace amounts of borate, chloride and fluoride in nuclear fuels employing ion chromatography (IC) after their extraction by pyrohydrolysis.

    Science.gov (United States)

    Jeyakumar, S; Raut, Vaibhavi V; Ramakumar, K L

    2008-09-15

    An accurate and sensitive method based on the combination of pyrohydrolysis-ion chromatography (PH-IC) is proposed for the simultaneous separation and determination of boron as borate, chloride and fluoride in nuclear fuels such as U(3)O(8), (Pu,U)C and Pu-alloys. The determination is based on the initial pyrohydrolytic extraction of B, Cl and F from the samples as boric acid, HCl and HF, respectively, which are subsequently separated by ion chromatography (IC). The proposed method significantly improves the existing analytical methodology as it combines the determination of boron, a critical trace constituent in nuclear materials, along with F(-) and Cl(-) for chemical quality control measurements. Various experimental parameters were optimized to achieve maximum recoveries of the analytes during the pyrohydrolysis and to get better ion chromatographic (IC) separation of borate, F(-) and Cl(-) along with other anions such as CH(3)COO(-), NO(2)(-), NO(3)(-), Br(-), PO(4)(3-) and SO(4)(2-). Recoveries of more than 93% could be obtained for all the analytes in the sample (0.5-1.5 g) at 1200+/-25K and distilled with pre-heated steam at the flow rate of 0.3 mL/min. An isocratic elution with a mobile phase of 0.56 M d-mannitol in 6.5mM NaHCO(3) was used for the IC separation. The detection limits for B (as borate), F(-) and Cl(-) were 24, 13 and 25 microgL(-1), respectively. Precision of about 5% was achieved for determination of boron, Cl(-) and F(-) in the samples containing 1-5 ppm(w) of boron, and 10-25 ppm(w) of Cl and F. The method was validated with reference materials and successfully applied to the nuclear fuels. The methodology is easy to adapt on routine basis. PMID:18761185

  16. Chloride in vesicular trafficking and function.

    Science.gov (United States)

    Stauber, Tobias; Jentsch, Thomas J

    2013-01-01

    Luminal acidification is of pivotal importance for the physiology of the secretory and endocytic pathways and its diverse trafficking events. Acidification by the proton-pumping V-ATPase requires charge compensation by counterion currents that are commonly attributed to chloride. The molecular identification of intracellular chloride transporters and the improvement of methodologies for measuring intraorganellar pH and chloride have facilitated the investigation of the physiology of vesicular chloride transport. New data question the requirement of chloride for pH regulation of various organelles and furthermore ascribe functions to chloride that are beyond merely electrically shunting the proton pump. This review surveys the currently established and proposed intracellular chloride transporters and gives an overview of membrane-trafficking steps that are affected by the perturbation of chloride transport. Finally, potential mechanisms of membrane-trafficking modulation by chloride are discussed and put into the context of organellar ion homeostasis in general. PMID:23092411

  17. 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。

  18. 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

  19. 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。

  20. Naked eye sensor on polyvinyl chloride platform of chromo-ionophore molecular assemblies: A smart way for the colorimetric sensing of toxic metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Prabhakaran, Deivasigamani; Nanjo, Hiroshi [Research Centre for Compact Chemical Process, National Institute of Advanced Industrial Science and Technology (AIST), Tohoku, 4-2-1 Nigatake, Miyagino-Ku, Sendai 983 8551 (Japan); Matsunaga, Hideyuki [Research Centre for Compact Chemical Process, National Institute of Advanced Industrial Science and Technology (AIST), Tohoku, 4-2-1 Nigatake, Miyagino-Ku, Sendai 983 8551 (Japan)], E-mail: hide.matsunaga@aist.go.jp

    2007-10-03

    We demonstrate the possibility of fabricating a simple, naked eye colorimetric sensor miniature, using chromo-ionophore molecular assemblies anchored on polyvinyl chloride (PVC) surface. The ion-sensing probe (4-n-dodecyl-6-(2-thiazolylazo)-resorcinol) provides a better efficiency with PVC platform in developing a series of colour transitions, while targeting trace levels of Cd{sup 2+}, Pb{sup 2+} and Hg{sup 2+}. The physical properties of the film sensor are controlled by measuring the probe isotherm plot. The surface morphology and molecular composition of the solid-state optical sensor are characterized using X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The changes in sensor's optical intensity and its response time for the target analytes are followed by absorption spectroscopy. High speed of response (t {<=} 5 min) and confidence in determination of analytes from chemically complex matrices has been achieved, using simulated synthetic mixtures and spiked real environmental samples, with a relative standard deviation of <3.9%. The proposed method offers consistent data reproducibility and reliability, with a detection limit of 0.031, 0.025 and 0.034 {mu}M, for Cd{sup 2+}, Pb{sup 2+} and Hg{sup 2+} ions, respectively. The sensor strips are reversible and reusable without any change in the sensing efficiency, up to four cycles. The signal response observed with the proposed method is consistent between sensors, and also are stable over time.

  1. 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.

  2. 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/.

  3. 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.

  4. Compressive strength and resistance to chloride ion penetration and carbonation of recycled aggregate concrete with varying amount of fly ash and fine recycled aggregate.

    Science.gov (United States)

    Sim, Jongsung; Park, Cheolwoo

    2011-11-01

    Construction and demolition waste has been dramatically increased in the last decade, and social and environmental concerns on the recycling have consequently been increased. Recent technology has greatly improved the recycling process for waste concrete. This study investigates the fundamental characteristics of concrete using recycled concrete aggregate (RCA) for its application to structural concrete members. The specimens used 100% coarse RCA, various replacement levels of natural aggregate with fine RCA, and several levels of fly ash addition. Compressive strength of mortar and concrete which used RCA gradually decreased as the amount of the recycled materials increased. Regardless of curing conditions and fly ash addition, the 28 days strength of the recycled aggregate concrete was greater than the design strength, 40 MPa, with a complete replacement of coarse aggregate and a replacement level of natural fine aggregate by fine RCA up to 60%. The recycled aggregate concrete achieved sufficient resistance to the chloride ion penetration. The measured carbonation depth did not indicate a clear relationship to the fine RCA replacement ratio but the recycled aggregate concrete could also attain adequate carbonation resistance. Based on the results from the experimental investigations, it is believed that the recycled aggregate concrete can be successfully applied to structural concrete members. PMID:21784626

  5. 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).

  6. Innovative leaching of cobalt and lithium from spent lithium-ion batteries and simultaneous dechlorination of polyvinyl chloride in subcritical water.

    Science.gov (United States)

    Liu, Kang; Zhang, Fu-Shen

    2016-10-01

    In this work, an effective and environmentally friendly process for the recovery of cobalt (Co) and lithium (Li) from spent lithium-ion batteries (LIBs) and simultaneously detoxification of polyvinyl chloride (PVC) in subcritical water was developed. Lithium cobalt oxide (LiCoO2) power from spent LIBs and PVC were co-treated by subcritical water oxidation, in which PVC served as a hydrochloric acid source to promote metal leaching. The dechlorination of PVC and metal leaching was achieved simultaneously under subcritical water oxidation. More than 95% Co and nearly 98% Li were recovered under the optimum conditions: temperature 350°C, PVC/LiCoO2 ratio 3:1, time 30min, and a solid/liquid ratio 16:1 (g/L), respectively. Moreover, PVC was completely dechlorinated at temperatures above 350°C without any release of toxic chlorinated organic compounds. Assessment on economical and environmental impacts revealed that the PVC and LiCoO2 subcritical co-treatment process had significant technical, economic and environmental benefits over the traditional hydrometallurgy and pyrometallurgy processes. This innovative co-treatment process is efficient, environmentally friendly and adequate for Co and Li recovery from spent LIBs and simultaneous dechlorination of PVC in subcritical water. PMID:27209515

  7. Molecular dynamics simulation study of ionic hydration and ion association in dilute and 1 molal aqueous sodium chloride solutions from ambient to supercritical conditions

    Science.gov (United States)

    Driesner, T.; Seward, T. M.; Tironi, I. G.

    1998-09-01

    The increasing demand for accurate equations of state of fluids under extreme conditions and the need for a detailed microscopic picture of aqueous fluids in some areas of geochemistry (e.g., mineral dissolution/precipitation kinetics) potentially make molecular dynamics (MD) simulations a powerful tool for theoretical geochemistry. We present MD simulations of infinitely dilute and 1 molal aqueous NaCl solutions that have been carried out in order to study the systematics of hydration and ion association over a wide range of conditions from ambient to supercritical and compare them to the available experimental data. In the dilute case, the hydration number of the Na + ion remains essentially constant around 5.5 from ambient to supercritical temperatures when the density is kept constant at 1 g cm -3 but decreases to below 5 along the liquid-vapor curve. In both cases, the average ion-first shell water distance decreases by about 0.03 Å from ambient to near critical temperatures. The Cl - ion shows a slight expansion of the first hydration shell by about 0.02 Å from ambient to near critical temperatures. The geometric definition of the first hydration shell becomes ambiguous due to a shift of the position of the first minimum of the Cl-O radial distribution function. In the case of the 1 molal solution, the contraction of the Na + first hydration shell is similar to that in the dilute case whereas the hydration number decreases drastically from 4.9 to 2.8 due to strong ion association. The released waters are replaced on a near 1:1 basis by chloride ions. Polynuclear clusters as predicted by Oelkers and Helgeson (1993b) are observed in the high temperature systems. The hydration shell of the Cl --ion shows significant deviation from the behavior in dilute systems, that is, at near vapor saturated conditions, the expansion of the hydration shell is significantly larger (0.12 Å from ambient to near critical temperatures). Due to a very large shift of the first

  8. Erosion Prediction of Chloride Ions in Existing Concrete under the Natural Tidal Environment by the Natural Diffusion Method%自然扩散法预测感潮环境下混凝土氯离子侵蚀

    Institute of Scientific and Technical Information of China (English)

    张俊芝; 郑辉; 周建民; 王梁英; 刘华挺

    2011-01-01

    通过对自然感潮环境下混凝土的自由氯离子浓度分布的分析,研究了既有混凝土氯离子侵蚀的特征及扩散特性,采用室内自然扩散法进行了模拟扩散试验,并根据Fick第二定律和Monte Carlo法分析了既有混凝土和试验混凝土的扩散参数及钢筋初始锈蚀时间.结果表明:自然环境下混凝土的氯离子侵蚀存在明显的对流区,自然扩散法的氯离子扩散系数大于自然环境下2个数量级,模拟混凝土中钢筋表面的自由氯离子浓度是自然环境下实际浓度的2倍,钢筋初始锈蚀时间是实际的240倍.%Characteristics of erosion and diffusion of free chloride ions in existing concrete are studied through analysis for chloride ion concentration distribution of concrete in the natural tidal environment, a simulation experiment for chloride ion diffusion by the indoor natural diffusion method is tested, diffusion parameters and the initial corrosion time of steel bar in concrete of existing concrete and experimental concrete are analyzed on the basis of Fick's second law and the Monte Carlo method. The experimental and analysis results show that there are obvious convective region of chloride ion ingress in the natural environment, the chloride diffusion coefficient measured by the natural diffusion method is two orders of magnitude larger than that in the natural tidal environment, and free chloride ion concentration of reinforcement surface in simulated concrete is double of actual concentration of concrete in the natural tidal environment,initial time of corrosion of steel bar in experimental concrete is 240 times higher than concrete in the natural environment.

  9. Thermodynamic properties of ions in solutions of sodium and potassium chlorides in H2O-DMSO and D2O-DMSO mixtures of 278-323 K

    International Nuclear Information System (INIS)

    Thermodynamic characteristics of sodium and potassium chlorides ion solvation in mixtures of water and heavy water with dimethylsulfoxide have been obtained from data on temperature dependence of the standard e.m.f. of circuits without transfer. Regularities in their change depending on cation nature, temperature and composition of mixed solvent have been considered. Isotope effect in the Gibbs free energy of ΣNa+, Cl- and ΣK+, Cl- solvation has been calculated. 20 refs.; 3 figs.; 2 tabs

  10. 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.

  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

    International Nuclear Information System (INIS)

    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. 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.

  13. 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)

  14. 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.

  15. 自动电位滴定法快速测定铝箔生产液中的氯离子%Automtic potentiometric titration determinated chloride ions in electrolyte

    Institute of Scientific and Technical Information of China (English)

    林庆宇; 张志; 罗杨合; 练洁婷

    2011-01-01

    利用自动电位滴定仪,在体积分数为80%的丙酮介质中,以Ag电极为指示电极,双盐桥甘汞电极为参比电极,对铝箔生产液中Cl-进行非水滴定,方法的电位突跃明显,电极响应速度较快,SO42-、Cu2+、Fe3+及可能存在其他离子均对测定结果无影响,实现了自动电位滴定法快速测定铝箔生产过程液中Cl-的含量,结果表明本法是一种测定Cl-含量的有效方法.%Using automatic potentiometric titration, chlorine ions in aluminum electrolyte was determined at 80% acetone medium, with the silver electrode as indicator electrode, double salt bridge calomel electrode as reference electrode. The end point jumped of method over 500mV, the electrode responsed faster. Sulfate, copper ions, iron ions and other ions were no effect on the determination. The result showed that content of chloride could be achieved quickly by automatic potentiometric titration. It is an effective way to determine of industry chloride ion.

  16. 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。

  17. Batch sorption dynamics and equilibrium for the removal of lead ions from aqueous phase using activated carbon developed from coffee residue activated with zinc chloride.

    Science.gov (United States)

    Boudrahem, F; Aissani-Benissad, F; Aït-Amar, H

    2009-07-01

    Lignocellulosic materials are good precursors for the production of activated carbon. In this work, coffee residue has been used as raw material in the preparation of powder activated carbon by the method of chemical activation with zinc chloride for the sorption of Pb(II) from dilute aqueous solutions. The influence of impregnation ratio (ZnCl2/coffee residue) on the physical and chemical properties of the prepared carbons was studied in order to optimize this parameter. The optimum experimental condition for preparing predominantly microporous activated carbons with high pore surface area (890 m2/g) and micropore volume (0.772 cm3/g) is an impregnation ratio of 100%. The developed activated carbon shows substantial capability to sorb lead(II) ions from aqueous solutions and for relative impregnation ratios of 75 and 100%, the maximum uptake is practically the same. Thus, 75% represents the optimal impregnation ratio. Batch experiments were conducted to study the effects of the main parameters such as contact time, initial concentration of Pb(II), solution pH, ionic strength and temperature. The maximum uptake of lead(II) at 25 degrees C was about 63 mg/g of adsorbent at pH 5.8, initial Pb(II) concentration of 10 mg/L, agitation speed of 200 rpm and ionic strength of 0.005 M. The kinetic data were fitted to the models of pseudo-first order and pseudo-second order, and follow closely the pseudo-second order model. Equilibrium sorption isotherms of Pb(II) were analyzed by the Langmuir, Freundlich and Temkin isotherm models. The Freundlich model gives a better fit than the others. Results from this study suggest that activated carbon produced from coffee residue is an effective adsorbent for the removal of lead from aqueous solutions and that ZnCl2 is a suitable activating agent for the preparation of high-porosity carbons. PMID:19447542

  18. Effect of volume fraction on chloride ion diffusion coefficient of grade structure concrete%体积分数对梯度结构混凝土扩散系数影响研究

    Institute of Scientific and Technical Information of China (English)

    温小栋; 干伟忠; 谷伟; 陈旭波

    2013-01-01

    通过室内氯离子侵蚀加速试验及氯离子分布测试,结合Fick第2定理拟合出梯度结构混凝土(GSC)的氯离子浓度扩散系数,以研究面层体积分数、加速试验龄期对扩散系数的影响;采用压汞技术测试面层材料与结构层材料的孔结构参数,分析氯离子扩散系数与孔结构之间的关系.结果表明:GSC体系的氯离子扩散系数随面层体积分数的增加而下降,并逐渐趋于平缓;GSC体系氯离子扩散系数则随加速试验龄期的延长而减小,最后也趋于稳定;与面层体积分数V=0试件相比,其它GSC试件具有更大的时间衰减系数值,说明其抵抗氯离子侵蚀的能力更好.最后根据相似性理论,建立了考虑面层体积分数变化的GSC氯离子扩散系数时变模型,分析显示,与结构层材料相比,面层材料具有较低的孔隙率及最可几孔径,使得孔的曲折性越大、连通性越低,因而面层材料具有更低的扩散系数.%Combined with the Fick' s Second Law the chloride ion diffusion coefficients of gradient structure concrete (GSC) were calculated for studying the effect of surface-layer volume fractions and accelerating period,by conducting the Chloride ion migration rapid test and determining the distribution of chloride ions.At the same time,the pore structure parameters were obtained by mercury intrusion porosimetry to study the relationship between chloride ion diffusion coefficient and pore structure parameters.The results show that chloride ion diffusion coefficient of the GSC is reduced with the increase of volume fractions of the surface-layer,and reaches a steady state finally; the chloride ion diffusion coefficient in GSC gradually decreases along with the increase of accelerating period,and also reaches a steady state finally.Compared with the specimens with 0 % volume fractions of surface-layer,the others with a higher volume fraction have a greater time decay coefficient of diffusion coefficient

  19. 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...

  20. Chloride ion transport in fly ash concrete under marine atmospheric environment%海洋大气中氯离子在粉煤灰混凝土中的传输规律

    Institute of Scientific and Technical Information of China (English)

    鲁彩凤; 袁迎曙; 季海霞; 姬永生

    2012-01-01

    为了实现海洋大气环境中粉煤灰混凝土耐久性使用寿命的预测,从氯离子在人工模拟海洋大气环境中粉煤灰混凝土中的传输试验出发,结合氯离子在非饱和多孔介质中的传输机理,研究海洋大气环境下混凝土内部微环境(微环境温度和相对湿度)及粉煤灰掺量对氯离子传输速率的影响程度,并与人工模拟海洋水下环境试验结果进行对比分析.研究结果表明:1)在海洋大气环境与海洋水下环境下,氯离子在粉煤灰混凝土中的扩散模型形式上一致,粉煤灰的掺人对氯离子传输能力有一定的影响,但不会改变氯离子在混凝土中的传输机理.2)当粉煤灰掺量一定时,微环境相对湿度越高(微环境温度一定),海洋大气环境氯离子扩散系数越大;但微环境温度(微环境相对湿度一定)对海洋水下环境和海洋大气环境中氯离子迁移的影响程度不同.3)粉煤灰掺量(微环境温度、相对湿度一定)对海洋水下环境和海洋大气环境氯离子扩散系数的影响规律不同.%The effect of micro-environment (temperature and relative humidity inside the concrete) and fly ash replacement on chloride ion transport in the fly ash concrete was analyzed from test results in artificial marine atmospheric zone and chloride diffusion mechanism in non-saturated porous media in order to predict durability service life. Then a comparative analysis between marine atmospheric environment and marine underwater environment was conducted. Results show that; l)the form of chloride diffusion model in fly ash concrete under atmosphere environment is consistent with that under underwater marine environment! the fly ash has a certain effect on chloride ion transport capacity, but it does not change the transport mechanism of chloride ion transport in fly ash concrete. 2) the higher the micro-environment relative humidity is (the same micro-environment temperature), the greater chloride ion

  1. 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.

  2. Nuevas determinaciones de isótopos estables para Tierra del Fuego

    OpenAIRE

    Guichón, Ricardo Aníbal; Borrero, Luis Alberto; Prieto, Luis A.; Cárdenas, Pedro; Tykot, Robert

    2001-01-01

    Se presentan los resultados del análisis de isótopos estables (d 13C y d 15N sobre colágeno, d 13C sobre apatita) de 8 muestras óseas procedentes de Tierra del Fuego que, junto con 15 determinaciones previas, informan sobre la variación en la subsistencia de poblaciones de cazadores-recolectores. Se observa que los valores más "marítimos" se encuentran en el conjunto Sudeste de la Isla Grande. Por otra parte, los más "continentales" se encuentran en el conjunto Norte de la Isla Grande. Es int...

  3. The removal of radioactive radium (Ra226) from chloride liquors by columnar ion exchange in the presence of calcium, magnesium and iron cations

    International Nuclear Information System (INIS)

    The purpose of this work was to study the feasibility of controlling the discharge of soluble Ra226, in the presence of Ca, Mg and Fe cations in synthetic chloride effluents, by adsorption on cation exchange resins to decrease Ra226-concentrations to federal environmental levels of 10 pCi Ra226/litre. Environmentally acceptable effluents were produced from synthetic chloride feed liquors containing 10 ppm Ca, 5 ppm Mg, 120 ppm Fe plus 20,000 pCi Ra226/litre. Environmentally acceptable effluents were not produced, by cation exchange, from a synthetic chloride liquor containing 490 ppm Ca, 97 ppm Mg, 720 ppm Fe in addition to 20,000 pCi Ra226/litre. The mass interference of the Ca + Mg + Fe cation concentrations in the feed liquor was in over-powering competition, for resin sites, with the Ra226-cations. To obtain realistic data, the adsorption process should be reexamined using a chloride liquor produced under optimal chloride leaching conditions of an Elliot Lake uranium ore. This would, in all probability, reveal other cations unavailable in the synthetic chloride liquors

  4. 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.

  5. 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...

  6. Determination of hydrolysis constants for gadolinium in ion strength media 2M of NaCl, NaClO{sub 4} and KCl at 303 K; Determinacion de las constanted de hidrolisis del gadolinio en los medios de fuerza ionica 2M de NaCl, NaClO{sub 4} y KCl, a 303 K

    Energy Technology Data Exchange (ETDEWEB)

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

    1999-07-01

    This work was made with the purpose to extend information about the hydrolysis constants of gadolinium (III) in ion strength media 2M of NaCl, NaClO{sub 4}, KCl at 303 K using the potentiometric method for this determination, and analysing starting from those data, the influence of anions and cations. It is concluded that the media which were determined the hydrolysis constants are very important and it is recommended the sodium perchlorate as the more adequate salt for those determinations. Also it was obtained the distribution diagrams of chemical species in each one of the media studied. (Author)

  7. 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.

  8. 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.

  9. 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

  10. Chloride ion-driven transformation from Ag3PO4 to AgCl on the hydroxyapatite support and its dual antibacterial effect against Escherichia coli under visible light irradiation.

    Science.gov (United States)

    Hong, Xiaoting; Li, Min; Shan, Shengdao; Hui, K S; Mo, Mingyue; Yuan, Xiaoli

    2016-07-01

    Visible light-driven photocatalytic inactivation of Escherichia coli was performed using hydroxyapatite-supported Ag3PO4 nanocomposites (Ag3PO4/HA). The antibacterial performance was evaluated by the methods of zone of inhibition plates and minimum inhibitory concentration test. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were employed to investigate the instability and transformation of the nanocomposite by comparing the crystalline, phase, and the morphology before and after exposure to Luria-Bertani culture medium under visible light irradiation. Ag3PO4 nanoparticles on the support were found to be shortly transformed into AgCl due to high chloride concentration of Luria-Bertani culture medium. The AgCl/HA nanocomposite showed both excellent intrinsic antibacterial performance contributed by the released silver ions and visible light-induced photocatalytic disinfection toward E. coli cells. This dual antibacterial function mechanism was validated by trapping the hydroxyl free radical and detecting the silver ions during the photocatalytic antibacterial process. The morphological change of E. coli cells in different reaction intervals was obtained by scanning electron microscopy (SEM) to complementally verify photocatalytic inactivation of E. coli. This work suggests that an essential comparison study is required for the antibacterial materials before and after the photocatalytic inactivation of bacterial cells using Ag3PO4 nanoparticles or Ag3PO4-related nanocomposites in mediums containing high-concentration chloride ions. PMID:27026549

  11. 骨料对氯离子在水泥基复合材料中扩散系数的影响%Influence of Aggregates on Chloride Ion Diffusion Coefficient in Cement-Based Composite Materials

    Institute of Scientific and Technical Information of China (English)

    孙国文; 孙伟; 张云升; 刘志勇; 王彩辉

    2011-01-01

    To determine the influence of aggregates on chloride ion diffusion coefficient in cement-based composite materials, mortar and concrete specimens were cast with different aggregates, aggregate size distributions and aggregate volume fractions. Pore size distributions and chloride ion diffusion coefficients of the specimens were measured by mercury intrusion porosimetry test and steady-state accelerated migration test, respectively. The volume fraction of interracial transition zone (ITZ) could be calculated according to the mix proportions of specimens, size distribution of aggregates and ITZ thickness. The results show that the chloride diffusivity in cement-based composite materials is related to the chloride diffusion coefficient of matrix and ITZ, volume fraction of aggregate and ITZ. The volume fraction of ITZ is affected by the aggregate size distribution, the volume fraction of aggregate and thickness of ITZ. The presence of aggregates in cement-based materials might modify the pore structure of hardened cement paste,and its dilution effect and tortuosity effect could reduce chloride transport properties. The special microstmctures of ITZ could increase chloride transport. The influence of ITZ could be dominant to chloride diffusion in cement-based materials. Based on the experimental and analytical results, the approximate chloride ion diffusion coefficient of ITZ is 13.26 or 18.45 times greater than the matrix migration coefficient for mortar or concrete, respectively.%为了确定骨料对氯离子在水泥基复合材料中扩散系数的影响,利用压汞技术和稳态电迁移法分别对含不同类型、不同粒径分布、不同体积分数骨料的砂浆和混凝土试样,进行了孔结构和氯离子扩散系数的测试,并根据试样配合比、骨料的粒径分布以及界面过渡区(简称界面区)厚度进行了界面区体积分数计算,最后提出了界面区有效扩散系数的预测模型.结果表

  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. Influence of fly ash on diffusion and binding of chloride ions in concrete%粉煤灰对混凝土中氯离子扩散与固化性能的影响

    Institute of Scientific and Technical Information of China (English)

    郭亚楠; 勾密峰; 李晓帆; 管学茂

    2014-01-01

    Natural diffusion method is used to measure the amount of free and total chloride ions of each diffusion depth in the normal concrete and fly ash concrete,and the binding capability of chloride is calculate at the same time.Results show that when the dosage of fly ash in concrete is 50%,the pore structure of concrete is improved by micro-aggregate effect and hydrated calcium silicate generated by pozzolan effect of fly ash,thus the performance of chloride diffusion is reduced;While its ability of chloride binding can be improved by calcium aluminate hydrates generated by pozzolan effect of fly ash.%采用自然扩散法测定了普通混凝土与粉煤灰混凝土各个扩散深度的总氯离子含量和自由氯离子含量,同时计算了混凝土对氯离子的固化能力。试验结果表明:混凝土中粉煤灰掺量为50%时,粉煤灰的微集料效应和火山灰效应生成的水化硅酸钙均改善了混凝土的孔结构,从而降低了氯离子的扩散性能;而粉煤灰的火山灰效应生成的铝酸盐水化物能够提高其固化氯离子的能力。

  14. 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).

  15. 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)

  16. A mathematical model for electrochemical chloride removal from marine cast iron artifacts

    Institute of Scientific and Technical Information of China (English)

    Weizhen OUYANG; Xia CAO; Ning WANG

    2009-01-01

    The aim of this article was to theoretically study diffusion and migration of chlo-ride ions during electrochemical chloride removal. The proposed model would enable optimization of its application by predicting the optimal treatment time and current combination. A mathematical model for simulating the transport behavior of chloride ions was developed by consideration of diffusion and migration of chloride ions when a constant DC current density was applied through the marine cast iron artifacts. The corresponding tests were conducted to validate the mathematical model. This model predicted the data of the extraction ratio of the chloride ion that correlated satisfac-torily with the experimental values. An important issue in electrochemical chloride removal was to understand how chloride ions moved, taking account of diffusion and migration of chloride ions and the release of binding chloride ions. The effects of the treatment time, externally applied current density, chloride diffusion coefficient, and rate constant of release of binding chloride ion on chloride removal are studied. The specific quantitative details applied to one-dimensional model were discussed here. This article has proposed a mathematical model for the first time, which was showed to be a useful tool that can reveal the ionic transport mechanism and optimize the application during electrochemical chloride removal.

  17. 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。

  18. 废弃玻璃骨料混凝土氯离子扩散的QR法%QR method for the chloride ion diffusion of the waste glass aggregate concrete

    Institute of Scientific and Technical Information of China (English)

    刘光焰; 范文; 王晓峰

    2014-01-01

    在Fick第二定律的基础上,根据废弃玻璃骨料混凝土中的氯离子基本方程,提出了用于废弃玻璃骨料混凝土氯离子扩散问题的QR法,建立了基于常扩散系数的氯离子扩散的QR法模型。通过算例,可知QR法具有很好的计算效率和很高的计算精度,同时,与其他方法相比,可以更好地计算非规则边界的氯离子扩散问题,而且该法集有限元法、有限条法、无限元法和样条有限点法的优点于一体,克服了有限元及有限条法的缺点,不仅计算简单,而且精度高,大大降低了离散未知量,降低了计算工作量,保证了计算精度和效率。%On base of the Fick's second law,the QR method for the question of the chloride ion diffusion of the waste glass aggregate concrete was researched according to the basic equation of the chloride ions and QR method.Through example ,research showed that QR method has good computational efficiency and high accuracy,while compared with other methods,it can better calculate non-regular boundary of the chloride ion diffusion problem.Moreover,the QR method gather many advantages of finite element method,finite strip method,infinite element method and the spline finite point and overcome shortcomings of the finite element and finite strip method.It is not only simple but also highly accurate,and it greatly reduces the discrete unknown variables and computational workload,and ensure the accuracy and efficiency.

  19. 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.

  20. 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.

  1. 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.

  2. Estimating the chloride transport in cement paste

    OpenAIRE

    Princigallo, A.

    2012-01-01

    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 prov...

  3. 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.

  4. Treatment of High-Concentration Chloride Ion Monosodium Glutamate Wastewater by Micro-electrolysis-Flocculation-UASB-SBR Technique%微电解-絮凝-UASB-SBR处理高浓度氯离子味精废水

    Institute of Scientific and Technical Information of China (English)

    袁雪; 房倬安; 徐中慧

    2011-01-01

    The micro-electrolysis-flocculation-UASB-SBR technique was adopted to treat high-concentration chloride ion monosodium glutamate wastewater. The results indicated that when the influent concentrations of COD and Cl~ were 3000 and 4000 mg/L, respectively, the effluent concentrations of COD and Cl~ could meet the discharge standard of pollutants for monosodium glutamate industry (GB19431-2004). The load of subsequent biochemical treatment was reduced and biodegradability of the wastewater was improved by use of the micro-electrolysis-flocculation technique. After three months of start-up,UASB could treat high-concentration chloride ion monosodium glutamate wastewater steadily and its effective removal rate was more than 70%. SBR with the intermittent aeration mode was an effective method to inhibit sludge bulking and to remove COD.%采用微电解-絮凝- UASB-SBR处理高浓度氯离子味精废水.运行结果表明:在进水COD的质量浓度为3 000 mg/L,氯离子的质量浓度高达4 000 mg/L时,出水水质能稳定达到味精工业污染物排放标准(GB19431-2004).采用微电解-絮凝组合能有效降低后续生化处理的负荷,提高废水的可生化性;上流式厌氧生物反应器(UASB)经过3个月的启动,能够稳定处理高氯离子味精废水,有效去除率达70%以上;序批式活性污泥法(SBR)采用间歇曝气方式,有效抑制了污泥膨胀,并能有效去除COD.

  5. Electrochemical behavior of lanthanum and yttrium ions in two molten chlorides with different oxoacidic properties: The eutectic LiCl-KCl and the equimolar mixture CaCl2-NaCl

    Directory of Open Access Journals (Sweden)

    Castrillejo Y.

    2003-01-01

    Full Text Available The electrochemical behavior of LaCl3 and YCl3 was studied in two molten chloride mixtures with different oxoacidic properties, the eutectic LiCl-KCl and the equimolar CaCl2-NaCl melt at different temperatures. The stable oxidation states of both elements have been found to be (III and (0 in both melts, and it was found that both La(III and Y(III cations were less solvated by the chloride ions in the calcium-based melt, which was explained by the stability of CaCl4 2- ions in that melt. Transient electrochemical techniques, such as cyclic voltammetry, chronopotentiometry and chronoamperometry were used in order to study the reaction mechanism and the transport parameters of electro active species at a tungsten electrode. The results showed that in the eutectic LiCl-KCl, the electro crystallization of lanthanum and yttrium seems to be the controlling electrochemical step while in CaCl2-NaCl this phenomenon has not been observed. That was explained in terms of the differences in the physicochemical properties of the systems, especially interfacial tensions. In the eutectic LiCl-KCl chronoamperometric studies indicated instantaneous and three dimensional nucleation and crystal growth of lanthanum and yttrium whatever the applied over potential of the rare earth metal is, whereas in the equimolar mixture CaCl2-NaCl, the corresponding electrochemical exchanges were found to be quasi-reversible, and the values of the kinetic parameters, K0 and α,were obtained for both reactions. Mass transport towards the electrode is a simple diffusion process, and the diffusion coefficients have been calculated. The validity of the Arrhenius law was also verified by plotting the variation of the logarithm of the diffusion coefficient versus 1/T.

  6. 缓凝剂对C50低氯离子混凝土性能的影响研究%Research on influence of retarders on the Performance of C50 low chloride ion concrete

    Institute of Scientific and Technical Information of China (English)

    徐长伟; 何桂春; 孟琦涵

    2014-01-01

    The influence of different kinds of retarder on the workability,volume change,strength,and hydration heat of C50 low chloride ion concrete were studied by using three kinds of retarders.Based on the design requirements of C50 high performance concrete,the content of chloride ion was controlled below 0.06%by adjusting and optimizing the mix proportion and the hydration heat was reduced by mixing right amount of fly ash.The results show that the fluidity loss can be effectively reduced and at the same time early volume deformation of concrete can be lowered without adverse effects on the late strength.Among the three kinds of retarders,the retarding effect of citric acid is stable.%采用三种缓凝剂来研究不同缓凝剂对C50低氯离子混凝土工作性、体积变化、强度和水化热的影响。基于C50高性能混凝土的设计要求,通过调整优化原料配比来实现混凝土中的氯离子含量在0.06%以下,并通过掺加适量的粉煤灰以达到降低水化热的目的。研究结果表明:掺加缓凝剂可以有效的减少混凝土的经时损失,同时降低混凝土早期体积变形,并对后期强度无不良影响。三种缓凝剂中,柠檬酸的缓凝效果比较稳定。

  7. Influence of chloride admixtures on cement matrix durability

    International Nuclear Information System (INIS)

    The influence of various inorganic salts, as chloride admixtures to Portland cement, on the mechanical properties and the durability of the matrix has been studied. The salts used in this study are chromium, nickel and cadmium chlorides. Improved compressive strength values are obtained which have been correlated to the stable metal hydroxide formation in high pH environment. Under static water conditions at 500C, hydrolyzed chloride ions exhibit adverse effects on the matrix durability through rapid release of calcium as calcium chloride in the initial period of leaching. On the contrary, enhanced matrix durability is obtained on long term leaching in the case of cement containing chromium chloride

  8. 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

  9. 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

    Science.gov (United States)

    Kouyoumdjian, H.; Saliba, N. A.

    2006-05-01

    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 (NH4)2SO4. 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(NO3)2 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 countries, relatively

  10. Intracellular chloride concentration of the mouse vomeronasal neuron

    OpenAIRE

    Kim, Sangseong; Ma, Limei; Unruh, Jay; McKinney, Sean; Yu, C. Ron

    2015-01-01

    Background The vomeronasal organ (VNO) is specialized in detecting pheromone and heterospecific cues in the environment. Recent studies demonstrate the involvement of multiple ion channels in VNO signal transduction, including the calcium-activated chloride channels (CACCs). Opening of CACCs appears to result in activation of VNO neuron through outflow of Cl− ions. However, the intracellular Cl− concentration remains undetermined. Results We used the chloride ion quenching dye, MQAE, to measu...

  11. Evaluation of Ag/AgCI sensors for in-situ monitoring of freee chloride concentration in reinforced concrete structures

    OpenAIRE

    Pargar, F.; Koleva, D.A.; Copuroglu, O.; Koenders, E.A.B.; Breugel, K. van

    2014-01-01

    The level of free chloride concentration in reinforced concrete structures essentially determines the onset of steel corrosion initiation and further propagation. One of the well-known methods for monitoring free chloride concentration is using silver/silver chloride electrodes (Ag/AgCl). These electrodes are sensitive mainly to chloride ions and establish a certain electrochemical potential depending on the chloride ion activity in the environment. Although the functioning principles of thes...

  12. Automatic Potential Titration of Thiocyanate and Chloride Ions in Black Nickel Plating Bath%黑镍镀液中硫氰酸根和氯离子的自动电位滴定

    Institute of Scientific and Technical Information of China (English)

    丘山; 丘星初; 曾家民; 刘星; 刘海燕

    2011-01-01

    The conditions and methods for automatic potential titration of thiocyanate and chloride ions were investigated. The results show that by selecting silver electrode as indication electrode, model 217 Double-liquid connecting electrode as reference electrode, the titration can be continuously operated in nitric acid medium, and these two kinds of ions can also be titrated by steps. When used in analyzing black nickel plating bath, it is easy and fast to operate, and the accuracy and precision can completely meet the demands of production.%研究了用自动电位滴定测定硫氰酸根和氯离子的条件及方法.结果表明:选用银电极为指示电极,217型双液接电极为参比电极,在硝酸介质中既能连续滴定也能分步滴定这两种离子.应用于黑镍镀液分析,方法简便快捷,分析的准确度和精密度完全能满足生产需要.

  13. 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. PMID:27245950

  14. 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.)

  15. Crystal Growth and Spectroscopic characterization of chloride and bromide single crystals doped with rare earth ions for the mid infrared amplification

    International Nuclear Information System (INIS)

    This work is devoted to the study of low phonon energy crystals doped with rare earth ions for the realisation of diode-pumped solid state laser sources emitting in the middle infrared. For that purpose, pure and (Er3+ or Pr3+) doped single crystals of KPb2Cl5 and Tl3PbX5 (X=Cl, Br) have been elaborated by using the Bridgman-Stockbarger method. These non-hygroscopic and congruent melting materials have been found to exhibit phase transitions during the cooling process but which do not limit the elaboration of centimeter-size single crystals. The spectroscopic study of the Er3+ doped compounds has been performed both at high and low temperatures. It thus appears that these systems present long fluorescence lifetimes and relatively large gain cross sections favorable for a laser emission around 4.5μm. It has been demonstrated further that the up-conversion processes resulting from excited-state absorptions of the Er3+ ions around the pumping wavelength as well as the energy transfer processes between the Er3+ ions do not lead to significant optical losses for the laser system. The derived parameters then have been used to build a model and simulate the laser operation of the system following diode pumping around 800 nm. In the end, the spectroscopic study of the Pr3+ ion in various materials has allowed us to evidence large emission cross sections associated with long fluorescence lifetimes, now favorable to a laser emission around 5μm. (author)

  16. 冻融影响掺合料再生混凝土抗氯离子渗透性能的试验研究%Experimental Study of Freeze-thaw's Influence on Resistance to Chloride Ion Penetration into Recycled Concrete with Mineral Admixture

    Institute of Scientific and Technical Information of China (English)

    王国林; 吴相豪; 杨姗姗

    2013-01-01

    The rapid chloride permeability test method (ASTM C1202) was used to research influences of freeze-thaw on anti-chloride-permeability performances of recycled concrete. The results showed that freeze-thaw cycle has clear implications for the anti-chloride-permeability performances of fly ash recycled concrete. With the increase of freeze-thaw times, the capacity of resistance to chloride ion permeability of fly ash recycled concrete decreased gradually. At the early stage of freeze-thaw, the ability of anti-chloride ion permeability of recycled concrete mixed with fly ash and lime powder is less affected by freeze-thaw. After 10 times freeze-thaw cycle, freeze-thaw has an ever-increasing impact on the anti-chloride ion ability of recycled concrete mixed with fly ash and lime powder.%  采用ASTM C1202法研究了冻融对掺合料再生混凝土抗氯离子渗透性能的影响规律。试验结果表明,冻融对粉煤灰再生混凝土抗氯离子渗透性能的影响比较大,随着冻融次数的增加,粉煤灰再生混凝土抗氯离子渗透能力逐渐减弱。冻融初期,冻融对粉煤灰-石灰粉再生混凝土抗氯离子渗透性能影响较小;冻融次数超过10次后,随着冻融次数的增加,冻融对粉煤灰-石灰粉再生混凝土抗氯离子渗透性能影响逐渐增强。

  17. 硫酸蒸煮法去除废糖蜜中氯离子的实验研究%Experimental study on removal of chloride ion in cane molasses by sulfuric acid cooking method

    Institute of Scientific and Technical Information of China (English)

    孟丹; 张海涛

    2013-01-01

    It is a kind of economic and environmental-friendly method that leaching manganese from a low-grade pyrolusite by cane molasses as reducing agent.But a certain amount of chloride ions is found in cane molasses,which will bring serious corrosion damage to the electrolytic anode plate in production practice.Chloride ions were removed from cane molasses and regenerating wastewater by sulfuric acid cooking method.The influences of reaction temperature,reaction time,and concentration of sulfuric acid were investigated.Results showed that using cane molasses treated under the conditions,i.e.mass fraction of H2SO4 was at 40%~45%,reaction time was 2 h,and reaction temperature was 80 ℃,to reduce the pyrolusite,the relative Mn leaching rate was 91.51%,meeting the requirements.%利用废糖蜜作还原剂,还原浸出低品位软锰矿,是一种经济环保的还原方法,但废糖蜜中含有一定的氯离子,在实际生产过程中会对电解阳极板产生严重的腐蚀破坏作用.实验通过硫酸蒸煮法去除废糖蜜和再生废水中的氯离子,考察了反应温度、反应时间和硫酸浓度等因素的影响.实验结果表明,在硫酸质量分数为40%~45%、反应时间为2h、反应温度为80℃的条件下处理废糖蜜还原软锰矿,相对浸出率可达91.51%,符合要求.

  18. 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

  19. 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....

  20. Determination of Anions in High Chloride Matrix by Ion Chromatography with Pre Online Sample Preparation Technique%谱睿在线除氯技术检测高氯水样中的阴离子

    Institute of Scientific and Technical Information of China (English)

    张夕虎; 刘肖

    2011-01-01

    We developed a method in which Dionex "Pre" online sample preparation technique was used to remove chloride by Ag cartridge and Na cartridge. This method is applicable to a wide range of samples and is simpler than offline approach. Each Ag cartridge carries on 400 consecutive injections (25 microlitre each) of 1% NaCl solution, and the removal efficiency is still above 99%. The separation of anions was carried out by high capacity hydroxide selectivity IonPac ASll-HC gradient separation column while Eluent Generator was employed to generate gradient KOH eluent online automatically. Two valves were switched to finish the injection. The system removes chloride well online for different matrix as analysis grade salt and sodium chloride. The detection limits of bromate, chlorate, chlorite, nitrite, nitrate and sulfate are less than 10μg/L, and the recoveries are between 80% and 110%. This method holds the advantages of easy-operation, good reproducibility, lower operation cost etc and is more convenient than off-line approach.%采用戴安公司谱睿(Pre)在线样品前处理技术,使用高容量在线Ag柱和Na柱,开发出了一种柱前去除高氯基体中氯离子的在线分析方法.操作简便,且适用样品范围广;不更换Ag柱可耐受10g/L NaCl基体,25μL连续进样400针,氯离子去除效率可保持在99%以上.系统选用高容量IonPac AS11-HC氢氧根体系阴离子交换色谱柱,在线淋洗液自动发生装置进行梯度淋洗,用抑制型电导检测.对食盐、分析纯氯化钠等不同基体进行检测,可实现样品在线除氯,并可检测其中不高于10μg/L的溴酸根、氯酸根、亚硝酸根、硝酸根和硫酸根等离子.不同离子校准曲线相关系数均在99.8%以上,加标回收率为80%~110%.该技术具有操作简单、可重复性强、方法新颖等特点,解决了以往高氯基体检测成本过高、适用范围有限、前处理操作复杂等问题.

  1. The role of bicarbonate ions and of adenosine 3',5'-monophosphate (cAMP) in chloride transport by epithelial cells of bullfrog small intestine.

    Science.gov (United States)

    Armstrong, W M; Youmans, S J

    1980-01-01

    In an HCO3-free medium, isolated segments of bullfrog small intestine, stripped of their external muscle layers, displayed a small, serosal positive PD that did not, on the average, differ significantly from zero. Similarly, in this medium, the mean values of Isc and of net Na+ and Cl- absorption under short-circuit conditions did not differ significantly from zero. External HCO3- (25 mM) induced a highly significant serosal negative PD and Isc and a large net absorption of Cl-. Net Cl- absorption exceeded Isc, i.e., there was a significant net flux, JR, which was consistent with a net secretion of HCO3-. The ratio of the internal Cl-activity of the absorptive cells (alpha Cli) to its equilibrium value was larger in the presence than in the absence of HCO3-. In the presence of HCO3-, cAMP, added to the serosal medium, reversed the serosal negative PD and Isc, and inhibited, though it did not completely abolish, net Cl- absorption. JR was unchanged; tissue Cl- and alpha Cli were reduced, and tissue Na+ decreased and tissue K+ increased. When HCO3- and Cl- were removed from the bathing medium, the electrical response of the tissue to cAMP, though greatly attenuated, was not completely abolished. Under these conditions, cAMP induced a significant net Na+ absorption. A model for ion transport in the absorptive cells of the small intestine is proposed that is consistent with these findings. PMID:6249145

  2. 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...

  3. 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.

  4. 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)

  5. 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

  6. Chloride ingress prediction

    DEFF Research Database (Denmark)

    Frederiksen, Jens Mejer; Geiker, Mette Rica

    2008-01-01

    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. 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

  8. Method for the Determination of Chloride Ion Flux with the Automatic Potentiometric Titration%自动电位滴定法测定焊剂中氯离子的方法

    Institute of Scientific and Technical Information of China (English)

    朵云琨; 邓勇; 朵云峰

    2014-01-01

    采用自动电位滴定法测定焊剂中氯离子的质量分数,对试样的处理、酸度的影响、线性范围、标准回收、精密度和准确度等进行探究.结果表明:对样品11次测定值的相对标准偏差(RSD)为2.27%~2.35%,标准回收率为99.00%~100.80%;所用方法的准确度和精密度较好,适合于焊剂中0.02%~1.00%氯离子的测定.%Using Auto-electric titration method measured Cl-in flux of mass fraction,the sample processing,the effects of acidity,linear range,standard recovery,precision and accuracy were studied.The results show that:the relative standard deviation of the measured val-ue of the samples for eleven times (RSD)ranged from 2.27%-2.35%;the standard recovery rate was 99.0%-100.8%;The accuracy and precision of the method are good,and suitable for the determination of 0.02%-1.00%in the flux of chloride ion.

  9. 上海市域地下水环境氯离子含量的时空演化特征研究%Study on the Temporal and Spatial Evolution Characteristics of Chloride Ion Content in the Groundwater Environment of Shanghai City

    Institute of Scientific and Technical Information of China (English)

    王玉强

    2015-01-01

    There is a wide distribution of Chloride Ion in groundwater, so it is of great significance to probe into the temporal and spatial dynamic evolution of Chloride content in groundwater environment. The results showed there existed a relevantly great change in the annual content of Chloride Ion in the groundwater of Shanghai City, presenting a regular quadric curve or cubic curve. Furthermore, the change in each aquifer presented a significant difference. From the perspective of its vertical distribution, the average content of Chloride Ion from height to lowness in turn was the second confined aquifer , the fifth confined aquifer, the unconfined aquifer, the fourth and the third confined aquifer.%鉴于氯离子在地下水中的分布很广,因此,探究地下水环境氯离子含量时空动态演化规律具有重要意义。研究发现,上海市地下水环境 Cl-含量年际演化幅度比较大,且呈现规律性的二次曲线或三次曲线,各个含水层之间的变化呈显著性差异。从其垂直方向分布看,氯离子平均含量由高到低依次为第二承压含水层,第五承压含水层,潜水含水层,第四承压含水层和第三承压含水层。

  10. Determination of chloride diffusion constants for concretes of differing water to cement ratios and admixtures

    OpenAIRE

    Smith, David Gilman

    1988-01-01

    Reinforced concrete exposed to chlorides is subject to rapid deterioration once the concentration of the chloride ion in the concrete reaches a critical level to cause corrosion of the reinforcing steel. The chloride ion diffuses through concrete according to Fick's Law, which is a function of time, a driving concentration, and a diffusion constant. The diffusion constant varies with temperature and the variety of concrete . The research included determination of diffusion ...

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

    OpenAIRE

    Mohammad K. Alkam; Maha Alqam

    2015-01-01

    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 ...

  12. Determination of the constants of the solubility product of Ln(OH)3 and the effect of the chloride ions on the lanthanum hydrolysis, praseodymium and lutetium in aqueous solutions of ion force 2 Molar

    International Nuclear Information System (INIS)

    The behavior of lanthanum (III), praseodymium (III), and lutetium (III) was studied in 2 M NaClO4 (aq) and 2 M NaCl (aq) at 303 K and free -CO2 conditions. Solubility diagrams (p Ln(aq)-pCH) were obtained by means of a radiochemical method. The pCH borderlines of saturation and unsaturation zones of the solutions and solubility product constants for Ln(OH)3 were determined from these diagrams. The fitting of the solubility equation to the experimental values of p Ln(aq)-pCH 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 LnCl2+ 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: logKps: 21.11 ± 0.09, 19.81 ± 0.11 and 18.10 ± 0.13 in 2M NaClO4; logKps: 22.22 ± 0.09, 21.45 ± 0.14 and 18.52 ± 0.29 in 2M NaCl; log β1: - 8.64 ± 0.02, - 8.37 ± 0.01 and - 7.95 ± 0.11 in 2M NaClO4; log β1/ : - 9.02 ± 0.11, - 8.75 ± 0.01 and - 8.12 ± 0.03 in 2M NaCl and the values for log β1,Cl were - 0.0255, - 0.155 and - 0.758, respectively. (Author)

  13. 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.

  14. 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

    2014-09-01

    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.

  15. 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. PMID:27105154

  16. 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.

  17. (tert-Butyl(2-hydroxyethylammonium chloride

    Directory of Open Access Journals (Sweden)

    Cintya Valerio-Cárdenas

    2014-07-01

    Full Text Available In the cation of the title molecular salt, C6H16NO+·Cl−, the N—C—C—O torsion angle is 176.5 (2°. In the crystal, the cations and chloride ions are linked by N—H...O and O—H...O hydrogen bonds, generating a two-dimensional network parallel to (100.

  18. The Study on Detection of Chloride Ion in Flue Gas Ammonium Sulfate Slurry by Automatic Potentiometric Titration Method%自动电位滴定法测定烟气氨法脱硫模拟浆液中氯离子的研究

    Institute of Scientific and Technical Information of China (English)

    杭蕾; 吕程; 陈慧慧; 连洲洋; 袁礼锐; 魏无际

    2015-01-01

    Chloride ion content of ammonia desulfurization process is an important monitoring indicators and this paper dis-cusses the detection of chloride ions in ammonium sulfate slurry by automatic potentiometric titration .The results show that :adding ethanol helps to increase the magnitude of the potential jump ;when pH=3-5 ,the result is accurate ;the recovery rate keeps between 90% and 110% ;compared with the Mohr method ,the test result is more accurate and precise and free from ash color;also the tested result is close to ion chromatography detection result ,but the high concentrations of chloride ion potentiometric titration is more advantageous .%氯离子含量是氨法脱硫工艺中的一个重要监控指标,用自动电位滴定法测定氨法脱硫浆液中的氯离子。结果表明,实验加入乙醇有利于增大电位突跃幅度;pH值为3~5时实验结果准确;加标回收率为90%~110%;与莫尔法相比,测定结果准确度、精密度更高,且不受灰分颜色干扰;与离子色谱法测定结果准确度、精密度相近,但测定高浓度氯离子电位滴定法更有优势。

  19. 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

  20. 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.

  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. Chloride removal from vitrification offgas

    International Nuclear Information System (INIS)

    This study identified and investigated techniques of selectively purging chlorides from the low-level waste (LLW) vitrification process with the purge stream acceptable for burial on the Hanford Site. Chlorides will be present in high concentration in several individual feeds to the LLW Vitrification Plant. The chlorides are highly volatile in combustion type melters and are readily absorbed by wet scrubbing of the melter offgas. The Tank Waste Remediation System (TWRS) process flow sheets show that the resulting chloride rich scrub solution is recycled back to the melter. The chlorides must be purged from the recycle loop to prevent the buildup of excessively high chloride concentrations

  3. Durability Analysis of Subway Station in Chloride Environment

    Directory of Open Access Journals (Sweden)

    Yang LuFeng

    2013-02-01

    Full Text Available 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 for durability analysis of subway station in chloride environment were also proposed.

  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. Relationship between chloride diffusivity and pore structure of hardened cement paste

    Institute of Scientific and Technical Information of China (English)

    Guo-wen SUN; Wei SUN; Yun-sheng ZHANG; Zhi-yong LIU

    2011-01-01

    Based on effective media theory, a predictive model, relating chloride diffusivity to the capillary pores, gel pores,tortuosity factor, and pore size distribution of hardened cement, is proposed. To verify the proposed model, the diffusion coefficient of chloride ions, the degree of hydration, and peak radius of capillary pores of cement paste specimens were measured. The predicted results for chloride diffusivity were compared with published data. The results showed that the predicted chloride diffusivity of hardened cement paste was in good agreement with the experimental results. The effect of the evolution of pore structures in cement paste on chloride diffusivity could be deduced simultaneously using the proposed model.

  6. Ion Channels, Natural Nanovalves

    OpenAIRE

    Eisenberg, Bob

    2012-01-01

    Ion channels are proteins with holes down their middle that control the flow of ions and electric current across otherwise impermeable biological membranes. The flow of sodium, potassium, calcium (divalent), and chloride ions have been central issues in biology for more than a century. The flow of current is responsible for the signals of the nervous system that propagate over long distances (meters). The concentration of divalent calcium ions is a 'universal' signal that controls many differ...

  7. 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.

  8. 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.

  9. 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...

  10. [Degradation of succinylcholine chloride].

    Science.gov (United States)

    Németh, G; Török, I; Paál, T

    1993-05-01

    Quantitative thin-layer chormatographic method has been developed for the investigation of the degradation of injection formulations containing succinylcholinium chloride. The method is based on the denistometric determination of the main degradation product, choline at 430 nm after visualization with iodine vapour. The stability of the injection was investigated under various storage conditions and it has been stated that considerable decomposition takes place during as short a period as one week. PMID:8362654

  11. 自动电位滴定法测定工业铬酸酐中氯离子含量方法研究%The Research Method to Determine Chloride Ion Content in Chromium Trioxide for Industrial Use with Automatic Potentiometric Titration

    Institute of Scientific and Technical Information of China (English)

    胡清启; 孙宁

    2015-01-01

    用乙醇作还原剂,将铬酸酐中CrO42-还原为Cr3+,再用硝酸银标准溶液滴定,以电位变化率最大点确定反应终点,求出氯离子含量。就精密度和加标回收进行实验,并对方法展开分析与讨论,该方法的建立对工业生产铬酸酐中氯离子指标的控制具有指导意义。%Reduce the CrO42+to Cr3+in chromium trioxide with ethanol as the reductant ,then determine the content of chloride ion using AgNO3 standard solution to titrate to the end point that has a biggest change of potential. Conduct an experiment for calculating the precision and standard addition recovery of the method,and then analysis and discuss about the method.This method has a guiding significance for controlling the content of chloride ion in the industrial production of chromium trioxide.

  12. 不同养护条件下低水胶比混凝土抗氯离子渗透性及孔结构试验研究%Study of the resistance to chloride ions penetration and pore structure of concrete with low water-binder ratio under various curing conditions

    Institute of Scientific and Technical Information of China (English)

    段运; 王起才; 张戎令; 谢超

    2016-01-01

    为研究不同养护条件对低水胶比混凝土抗氯离子渗透性和孔结构的影响规律及程度,采用气孔分析法、压汞法和RCM法、电通量法对不同养护条件下低水胶比混凝土28 d孔结构和抗氯离子渗透性进行测试。试验结果表明:负温(-3℃)和低温(3℃)养护条件下,低水胶比混凝土比其标准养护条件下孔径明显粗化,大孔数量增多,小孔数量减少,气孔间距系数和气孔平均直径增大;低水胶比混凝土中多害孔和有害孔数量、临界孔径和最可几孔径明显比其标准养护条件下大,且负温养护条件下增大程度更大;低水胶比混凝土28 d电通量和氯离子迁移系数明显大于其标准养护条件下的混凝土,抗氯离子渗透性能明显降低;负温养护条件下,混凝土抗氯离子渗透性能下降程度很大,主要是由于负温不仅使孔的连通性增强、孔径粗化和劣化,而且对混凝土内部孔结构造成了一定程度的不可恢复的损伤。%In order to study the influencing mechanism of various curing conditions on the resistance to chloride i-ons penetration and pore structure of concrete with low water-binder ratio,porosity analysis,mercury injection method,Electric flux method and RCMmethod were adopted in the study.These methods were used in the experi-ment to test the pore structure and the resistance to chloride ions penetration of the low water-binder ratio concrete after curing 28d.The result shows that the aperture of concrete with low water-binder ratio after being cured un-der minus temperature (-3℃)and low temperature (3℃)is obviously roughened than is cured under standard conditions.The number of larger aperture increases,while the number of smaller apertures decreases.The bubbles spacing factor and average pore size increase.The number of more harmful holes,the critical aperture and maxi-mum probability aperture in concrete with low water

  13. Novel vanadium chloride/polyhalide redox flow battery

    Science.gov (United States)

    Skyllas-Kazacos, Maria

    This paper describes a novel redox flow cell which employs a polyhalide solution in the positive half-cell electrolyte and a vanadium(II)/vanadium(III) chloride redox couple as the negative half-cell electrolyte. During charging, the bromide ions in the positive half-cell are considered to undergo oxidation to the polyhalide ion Br 2Cl -; the formal potential of this couple is about 0.8 V versus the saturated calomel electrode (SCE). When combined with a formal potential of around -0.5 V versus SCE for the V(III)/V(III) coupled in the chloride supporting electrolyte, an overall cell potential of approximately 1.3 V would be expected for the vanadium chloride/polyhalide redox flow cell.

  14. 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.

  15. Reaction of uranium dioxide with copper-containing chloride melts

    International Nuclear Information System (INIS)

    Cermet composition materials consisting of metallic copper and uranium dioxide can be used for manufacturing fuel rods of nuclear power reactors. Reprocessing of such irradiated fuel of dispersive type can be done employing non-aqueous pyrochemical methods and developing such technology requires information on interaction of uranium dioxide with chloride melts containing copper ions

  16. (tert-Butyl)(2-hydroxyethyl)ammonium chloride

    OpenAIRE

    Cintya Valerio-Cárdenas; Simón Hernández-Ortega; David Morales-Morales

    2014-01-01

    In the cation of the title molecular salt, C6H16NO+·Cl−, the N—C—C—O torsion angle is 176.5 (2)°. In the crystal, the cations and chloride ions are linked by N—H...O and O—H...O hydrogen bonds, generating a two-dimensional network parallel to (100).

  17. 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。

  18. 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. PMID:10624900

  19. 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

    of this compoundscontaining a dimeric ion-pair “molecule”swas investigated in the solid state, in solutions in water and ethanol, and in the vapor phase, based on ab initio molecular orbital density functional theory (DFT)-type calculations with 6-311+G(d,p) basis sets. Calculations on the monomeric [TMGH]+ ion...

  20. 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

  1. Influence of Fly Ash on Surface Chloride Concentration Under Shallow Immersion Condition

    OpenAIRE

    Liu, Jun; Wang, Xiaodong; Xing, Feng; Han, Ningxu

    2014-01-01

    In this paper, the influence of fly ash content on concrete surface chloride concentration was investigated through periodical tests of surface chloride concentration of concrete by immersing three kinds of concrete specimens in 5.0 wt.% sodium chloride solution. One kind of specimen is common concrete without fly ash, whereas the other two kinds of specimens are mixed with fly ash. The results show that the surface chloride ion concentration ranges from 0.295 to 0.777 wt.% for the immersed c...

  2. Indium sulfide precipitation from hydrochloric acid solutions of calcium and sodium chlorides

    International Nuclear Information System (INIS)

    The effect of precipitation duration, acid concentration, indium complexing with chloride ions on the process of indium sulfide chemical precipitation in hydrochloric acid solutions, precipitate composition and dispersity are studied. It is established that indium sulfide solubility increases in solutions with acid concentration exceeding 0.40-0.45 mol/l. Calcium and indium chloride addition to diluted hydrochloric solutions greatly increases the solubility of indium sulfide. The effect of calcium chloride on In2S3 solubility is higher than that of sodium chloride

  3. Valyl benzyl ester chloride

    Directory of Open Access Journals (Sweden)

    Grzegorz Dutkiewicz

    2010-02-01

    Full Text Available In the title compound (systematic name: 1-benzyloxy-3-methyl-1-oxobutan-2-aminium chloride, C12H18NO2+·Cl−, the ester group is approximately planar, with a maximum deviation of 0.040 (2 Å from the least-squares plane, and makes a dihedral angle of 28.92 (16° with the phenyl ring. The crystal structure is organized by N—H...Cl hydrogen bonds which join the two components into a chain along the b axis. Pairs of chains arranged antiparallel are interconnected by further N—H...Cl hydrogen bonds, forming eight-membered rings. Similar packing modes have been observed in a number of amino acid ester halides with a short unit-cell parameter of ca 5.5 Å along the direction in which the chains run.

  4. 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... dichloride, vinyl chloride and polyvinyl chloride plants. An owner or operator of an ethylene dichloride, vinyl chloride, and/or polyvinyl chloride plant shall comply with the requirements of this section....

  5. 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.

  6. 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)

  7. Sodium chloride, potassium chloride, and virulence in Listeria monocytogenes.

    OpenAIRE

    MYERS, E. R.; Dallmier, A W; Martin, S E

    1993-01-01

    Virulence, as determined in a mouse model, and the virulence factor activities of catalase, superoxide dismutase, and listeriolysin O were examined in a parental strain (10403S) and in a nonhemolytic mutant strain (DP-L224) of Listeria monocytogenes. The cells were propagated in media containing various concentrations of sodium chloride or potassium chloride. Strains 10403S and DP-L224 exhibited significant increases in catalase activity and listeriolysin O activity when grown in medium conta...

  8. 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.

  9. Adsorption of Tetradecylpyridinium Chloride on Aqueous Surfaces of Sodium Chloride Solutions

    OpenAIRE

    Fujio, Katsuhiko; Hayashi, Koji; Suzuki, Maki

    2014-01-01

    Surface tension of aqueous NaCl solutions of tetradecylpyridinium chloride (TPC) has been measured by the drop weight method at different NaCl concentrations from 0 to 1.000 mol dm−3 at 25◦C. Surface excess densities of tetradecylpyridinium ion (TP+), Cl− and Na+ have been obtained as functions of TPC concentration at different NaCl concentrations by applying the Gibbs adsorption isotherm to the surface tension data below the critical micelle concentration (CMC) of TPC. Surface excess densiti...

  10. Adsorption of Dodecylpyridinium Chloride on Aqueous Surfaces of Sodium Chloride Solutions

    OpenAIRE

    Fujio, Katsuhiko; TAKEUCHI, Kumiko; Suzuki, Maki

    2012-01-01

    Surface tension of aqueous NaCl solutions of dodecylpyridinium chloride (DPC) has been measured by the drop weight method at different NaCl concentrations from 0 to 1.000 mol dm-3 at 25℃. Applying the Gibbs adsorption isotherm to the surface tension data at DPC concentrations below the critical micelle concentration (CMC), surface excess densities of dodecylpyridinium ion (DP+), Cl- and Na+ have been obtained as functions of DPC concentration at different NaCl concentrations. Surface excess d...

  11. 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.

  12. Influence of sulphates on chloride diffusion and the effect of this on service life prediction of concrete in a submerged marine environment

    OpenAIRE

    Maes, M; Caspeele, R.; Van den Heede, P.; De Belie, N.

    2012-01-01

    Single-ion attack by chlorides and multi-ion attack by chlorides and sulphates were compared with respect to the full probabilistic service life prediction of concrete structures, according to fib Bulletin 34. Especially the influence of sulphates on the chloride diffusion coefficient was investigated more thoroughly. Four concrete mixtures were tested, two Portland cement concretes and two blast-furnace slag concretes. Migration tests and natural diffusion tests were executed, based on NT bu...

  13. Crystal structure of Halobacterium salinarum halorhodopsin with a partially depopulated primary chloride-binding site.

    Science.gov (United States)

    Schreiner, Madeleine; Schlesinger, Ramona; Heberle, Joachim; Niemann, Hartmut H

    2016-09-01

    The transmembrane pump halorhodopsin in halophilic archaea translocates chloride ions from the extracellular to the cytoplasmic side upon illumination. In the ground state a tightly bound chloride ion occupies the primary chloride-binding site (CBS I) close to the protonated Schiff base that links the retinal chromophore to the protein. The light-triggered trans-cis isomerization of retinal causes structural changes in the protein associated with movement of the chloride ion. In reverse, chemical depletion of CBS I in Natronomonas pharaonis halorhodopsin (NpHR) through deprotonation of the Schiff base results in conformational changes of the protein: a state thought to mimic late stages of the photocycle. Here, crystals of Halobacterium salinarum halorhodopsin (HsHR) were soaked at high pH to provoke deprotonation of the Schiff base and loss of chloride. The crystals changed colour from purple to yellow and the occupancy of CBS I was reduced from 1 to about 0.5. In contrast to NpHR, this chloride depletion did not cause substantial conformational changes in the protein. Nevertheless, two observations indicate that chloride depletion could eventually result in structural changes similar to those found in NpHR. Firstly, the partially chloride-depleted form of HsHR has increased normalized B factors in the region of helix C that is close to CBS I and changes its conformation in NpHR. Secondly, prolonged soaking of HsHR crystals at high pH resulted in loss of diffraction. In conclusion, the conformation of the chloride-free protein may not be compatible with this crystal form of HsHR despite a packing arrangement that hardly restrains helices E and F that presumably move during ion transport. PMID:27599860

  14. 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.

  15. NaCl胁迫对甘薯试管苗生长和离子含量的影响%Effects of Sodium Chloride Stress on Growth of Sweet Potato Plantlets in vitro and Ion Content

    Institute of Scientific and Technical Information of China (English)

    高叶; 赵术珍; 陈敏; 宋晓征; 王宝山

    2008-01-01

    [Objective] This study aimed to investigate the salt-tolerance mechanism of sweet potato. [Method] Two sweet potato varieties of Xu 25-2 (salt-tolerant cuhivar) and Triumph 100 (salt-sensitive cultivar) were treated by sodium chloride with the concentration of 0 mmol/L and 100 mmol/L. After 20 days, Na+ content and Na+/K+ ratio in the roots, shoots and leave were determined by the flame photometer, while dry weight and fresh weight of roots, shoots and leave in different varieties were also studied. [Result] The growth of two sweet potato varieties was inhibited under salt stress, so the plant became shorter, leaf and root became fewer, dry weight of roots and leave decreased, but seedlings of Xu 25-2 were inhibited slightly. Furthermore, Na+ content and Na+/K+ ratio in roots, shoots and leaves of two sweet potato varieties increased. Na+ content of salt-tolerant Xu 25-2 was low in roots, shoots and leaves, while Na+ content of salt-sensitive Triumph 100 was high in shoots and leave of seedlings, but the change range of Xu 25-2 was less than that of Triumph 100. [Conclusion] The lower Na+ content and Na+/K+ ratio in leaves under salt stress were the most important characteristics for salt-tolerance of sweet potato varieties.

  16. N,N-Dimethyldehydroabietylammonium chloride ethanol monosolvate

    Directory of Open Access Journals (Sweden)

    Xiu-Zhi Huang

    2013-06-01

    Full Text Available The title compound {systematic name: 1-[(1R,4aS,10aR-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthren-1-yl]-N,N-dimethylmethanaminium chloride ethanol monosolvate}, C22H36N+·Cl−·C2H6O, was synthesized from dehydroabietylamine by N-methylation with formaldehyde/formic acid and transformation into the hydrochloride. The dehydroabietyl moiety exhibits the usual conformation with the two cyclohexane rings in chair and half-chair conformations and a trans-ring junction. The crystal structure is built up from columns of the dehydroabietyl moieties stacked along the a axis. These columns are held together by the chloride ions via N—H...Cl and C—H...Cl interactions, which establish a two-dimensional network parallel to (010. The ethanol solvent molecules are located between the columns and anchored via O—H...Cl hydrogen bonds.

  17. Swell activated chloride channel function in human neutrophils

    Energy Technology Data Exchange (ETDEWEB)

    Salmon, Michael D. [Leukocyte and Ion Channel Research Laboratory, School of Health and Biosciences, University of East London, Stratford Campus, London E15 4LZ (United Kingdom); Ahluwalia, Jatinder, E-mail: j.ahluwalia@uel.ac.uk [Leukocyte and Ion Channel Research Laboratory, School of Health and Biosciences, University of East London, Stratford Campus, London E15 4LZ (United Kingdom)

    2009-04-17

    Non-excitable cells such as neutrophil granulocytes are the archetypal inflammatory immune cell involved in critical functions of the innate immune system. The electron current generated (I{sub e}) by the neutrophil NADPH oxidase is electrogenic and rapidly depolarises the membrane potential. For continuous function of the NADPH oxidase, I{sub e} has to be balanced to preserve electroneutrality, if not; sufficient depolarisation would prevent electrons from leaving the cell and neutrophil function would be abrogated. Subsequently, the depolarisation generated by the neutrophil NADPH oxidase I{sub e} must be counteracted by ion transport. The finding that depolarisation required counter-ions to compensate electron transport was followed by the observation that chloride channels activated by swell can counteract the NADPH oxidase membrane depolarisation. In this mini review, we discuss the research findings that revealed the essential role of swell activated chloride channels in human neutrophil function.

  18. 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.

  19. 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.

  20. Durability of Steel Fibres Reinforcement Concrete Beams in Chloride Environment Combined with Inhibitor

    Directory of Open Access Journals (Sweden)

    AbdelMonem Masmoudi

    2016-01-01

    Full Text Available This paper presented the effect of the combination of an inhibitor and steel fibre reinforced concrete (SFRC for concrete structures in chloride environments. Twelve beams were cast and tested to study their flexural behavior. The morphology of steel surfaces using the inhibitor after observing the scanning electron microscope showed a low layer of corrosion products. The steel surface immersed in the inhibitor free solution was seen to have been subject to chloride ions attacks as shown in this study. The interest to the field of the present study is the relatively higher durability of the performance when using the inhibitor. Crack width and crack spacing for beams under the same load showed that the use of SFRC with the inhibitor for concrete structures in chloride environments must have transferred tension across cracks that led to reducing crack spacing without any chloride ions attack.

  1. 活性粉末混凝土微观结构及其对强度与抗氯离子渗透性能的影响研究%Influence of micro-structure on the strength and resistance to chloride ion permeability of reactive powder concrete

    Institute of Scientific and Technical Information of China (English)

    余自若; 高康; 安明喆; 韩松

    2013-01-01

    The samples of reactive powder concrete mixed with various mineral admixtures were prepared and tested to investigate the strength and electric flux. The hydration products, pore-structure and micro-structure were studied by X-ray diffraction (XRD), mercury intrusion porosimetry (MIP) and scanning electron microscope (SEM). The high strength and resistance to chloride ion permeability mechanism of RPC was discussed. The results indicated that the content of silica fume is the most important factor to enhance the performance of reactive powder concrete. The porosities of samples incorporated with mineral powder and metakaolin are lower than those samples which contain silica fume only. As cured with high temperature, metakaolin is more powerful in improving the resistance to chloride ion permeability than mineral powder. With the increasing of curing temperature, the strength and resistance to permeability are increased obviously, and this character is not influenced by the changing of mineral raw materials blending method.%在多种矿物掺合料混掺的活性粉末混凝土的强度和电通量试验基础上,运用x射线衍射分析(XRD)、汞压力测孔分析(MIP)及扫描电镜观察(SEM)技术,研究了活性粉末混凝土的主要水化产物、孔结构和微观形貌,探讨了各种矿物掺合料对活性粉末混凝土的强度和抗氯离子渗透性的影响机理.研究结果表明,在各种活性粉末对混凝土的性能增强作用中,硅粉的含量是最主要的因素;掺入矿粉和偏高岭土的活性粉末混凝土样品,比单一使用硅粉的样品孔隙率略低;高温养护下偏高岭土在提高材料抗氯离子渗透性方面的作用比矿粉明显;不论对于哪一种矿物原料的掺合方式,活性粉末混凝土的强度和抗氯离子渗透性能都随着养护温度的提高而有所增强.

  2. Stability of succinylcholine chloride injection.

    Science.gov (United States)

    Schmutz, C W; Mühlebach, S F

    1991-03-01

    The stability of succinylcholine chloride injection prepared by a hospital pharmacy was studied under a wide variety of conditions. Batches of succinylcholine chloride injection 10 mg/mL containing sodium chloride, methyl-4-hydroxybenzoate, hydrochloric acid, and water were prepared. Samples were tested for the effect of initial pH (3.0 and 4.2) and sterilization (steam treatment at 100 degrees C for 30 minutes and 121 degrees C for 20 minutes) on stability after three weeks; long-term stability under refrigeration (12, 17, and 23 months of storage at 4 degrees C); and the effect of storage temperature (4-6 degrees C, 20-26 degrees C, 35 degrees C, and 70 degrees C) and light exposure at various intervals up to 12 months. Samples were analyzed by thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC). Unlike heating at 121 degrees C, heating at 100 degrees C produced no significant loss of succinylcholine chloride, independent of the initial pH. Succinylcholine chloride was hydrolyzed only minimally over 23 months if the solution was stored at 4-6 degrees C. A 10% loss of drug content occurred if solutions were kept at 20-26 degrees C for five months, at 35 degrees C for one month, or at 70 degrees C for one day. Initial degradation was slowed if the solution was protected from light. The assessments by TLC proved to be more sensitive than the HPLC measurements. Succinylcholine chloride injection sterilized at 100 degrees C for 30 minutes can be stored for up to five months at room temperature if protected from light. The preparation is stable for at least two years under refrigeration. PMID:2028996

  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. cis-Dichloridobis(1,10-phenanthroline)chromium(III) chloride

    OpenAIRE

    Xiaoli Gao

    2011-01-01

    In the title complex, [CrCl2(C12H8N2)2]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.

  5. 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...

  6. Crevice corrosion of alloy 22 in fluoride and chloride containing solutions

    International Nuclear Information System (INIS)

    Alloy 22 (N06022) is highly resistant to localized corrosion. Alloy 22 may be susceptible to crevice corrosion in pure chloride (Cl-) solutions under aggressive environmental conditions. The effect of the fluoride (F-) on the susceptibility to crevice corrosion induced by chloride ions is still not well established. The objective of the present work was to explore the crevice corrosion resistance of this alloy to different mixtures of fluorides and chlorides. Cyclic potentiodynamic polarization (CPP) tests were conducted in deaerated aqueous solutions of pure halide ions and also in different mixtures of chloride and fluoride at 90 C degrees and pH 6. The range of chloride concentration [Cl-] was 0.001 M ≤ [Cl-] ≤ 1 M and the range of molar fluoride to chloride ratio [F-]/[Cl-] was 0.1≤ [F-]/[Cl-] ≤ 10. Results showed that Alloy 22 was susceptible to crevice corrosion in all the pure chloride solutions but not in the pure fluoride solutions. A molar ratio [F-]/[Cl-] ranging from 5 to 10 was required for the inhibition of crevice corrosion to be complete in the halide mixtures. A moderate or nil inhibitive effect was observed for molar ratios [F-]/[Cl-] < 5. (author)

  7. A study of Trace Gold Chloride and Hydroxide Speciation in Weak Alkaline Solution by Ion Chromatography-Inductively Coupled Plasma Mass Spectrometry%离子色谱电感耦合等离子体质谱研究痕量氯金酸在弱碱性体系中金(Ⅲ)的形态

    Institute of Scientific and Technical Information of China (English)

    刘德晔; 朱醇; 马永建

    2012-01-01

    A method based on ion chromatography-inductively coupled plasma mass spectrometry(IC-ICP-MS) was developed to study trace gold chloride and hydroxide speciation in weak alkaline solu-tion. The results revealed that, the main compounds in weak alkaline solution were [AuCl2(OH)2]~ and [AuCKOH)3]-when the total Au mass was between 4. 0 30 ng. Unlike high HAuCl4 4H2O concentration, trace [AuCl2 (OH)2]~ could exist between pH 7. 0 to 10. 0, at least. Additional chlo-ride brought promotion to [AuCl2(OH)2]~ and reduction to CAuCl(OH)3]~. When pH was 7. 0 or chloride concentration was above 0. 050 mol/L, AuflE) would generate a compound which could not be flushed out of chromatography system. According to hydrolysis process. that compound was deduced as [AuCl3(OH)]-. The equilibrium constant K3 of [AuCl2(OH)2]- + OH ←[AuCl (OH)3]-+Cl always changed with pH values and chloride concentrations. Therefore, there might exist other factor to influence the trace Au(Ⅲ) hydrolysis.%采用离子色谱电感耦合等离子体质谱联用方法研究弱碱性体系下痕量氯金酸中Au(Ⅲ)的形态.结果表明:在弱碱性条件下,总金含量在4.0~30 ng之间,Au(Ⅲ)主要以[AuCl2( OH)2]-和[AuCl(OH)3]-的形式存在.与较高含量的氯金酸溶渡相比,痕量氯金酸溶液中的[AuCl2(OH)2]-至少可以在pH 7.0~10.0范围内存在.溶液外加的Cl-可使[AuCl2 (OH)2]-含量升高同时降低[AuCl (OH)3]-含量;当pH=7.0或Cl-浓度高于0.050 mol/L,会产生不随色谱流出的金络合物,根据水解过程推断该络合物为[AuC13 (OH)]-.在pH 8.0~10.0,Cl-浓度在0.000~0.020 mol/L时,[AuCl2(OH)2]-+OH-=[AuCl (OH)3]-+Cl-的水解平衡常数为不定值,说明痕量氯金酸的水解不仅受pH值和Cl-浓度影响,还受其它因素影响.

  8. 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.

  9. 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

  10. 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.

  11. 氯离子对2种牙科常用合金耐腐蚀性的影响%Effect of chloride ion on corrosion of two commonly used dental alloys

    Institute of Scientific and Technical Information of China (English)

    陈蕾; 张维丹; 张媛媛

    2014-01-01

    Objective: To investigate the effect of chloride concentration on the corrosion of Co-Cr alloy and pure Ti in a simulated oral environment. Methods: The electrochemical corrosion tests of pure Ti and Co-Cr alloy were carried out in neutral artiifcial saliva solutions with different NaCl concentrations (0.9%, 2.0%, and 3.0%). hTe morphologies of corroded surface for pure Ti and Co-Cr alloy were observed by scanning electron microscope (SEM). Results: hTe changes in the self-corrosion potentials (Ecorr) for pure Ti and Co-Cr alloy in three kinds of artificial saliva solutions was not obvious. However, the self-corrosion current densities (Icorr) of pure Ti were much lower than those of Co-Cr. TheIcorr of Co-Cr alloy increased in a concentration-dependent manner of NaCl, whereas the breakdown potential (Eb) of Co-Cr alloy decreased in a concentration-dependent manner. hTe potential ranged for the breakdown of oxide film (Ev) was shortened in a concentration-dependent manner of NaCl. There was no obviousdifference in theIcorr of pure Ti with different concentrations of NaCl. hTe breakdown potential was not seen according to the polarization curves. Conclusion: In a certain range, the increase of the concentration of Cl- leads to accelerate the corrosion behavior of Co-Cr alloy, but it does not affect pure Ti.%目的:在模拟口腔环境下,探讨氯离子对钴铬合金和纯钛耐腐蚀性的影响。方法:通过对两种合金在不同NaCl(0.9%,2.0%,3.0%)浓度的中性人工唾液中进行电化学腐蚀指标测试并结合扫描电镜(SEM)扫描,观察其表面形貌。结果:钴铬合金和纯钛在三种人工唾液中的自腐蚀电位(Ecorr)的变化趋势无明显规律性,但是纯钛的自腐蚀电流密度(Icorr)明显小于钴铬合金。钴铬合金的自腐蚀电流密度随NaCl浓度的升高而增大,破裂电位值随NaCl浓度的升高而降低,氧化膜阳极破裂前的电位区间随NaCl浓度的升高而降低。纯钛的

  12. Simultaneous optical recording in multiple cells by digital holographic microscopy of chloride current associated to activation of the ligand-gated chloride channel GABA(A receptor.

    Directory of Open Access Journals (Sweden)

    Pascal Jourdain

    Full Text Available Chloride channels represent a group of targets for major clinical indications. However, molecular screening for chloride channel modulators has proven to be difficult and time-consuming as approaches essentially rely on the use of fluorescent dyes or invasive patch-clamp techniques which do not lend themselves to the screening of large sets of compounds. To address this problem, we have developed a non-invasive optical method, based on digital holographic microcopy (DHM, allowing monitoring of ion channel activity without using any electrode or fluorescent dye. To illustrate this approach, GABA(A mediated chloride currents have been monitored with DHM. Practically, we show that DHM can non-invasively provide the quantitative determination of transmembrane chloride fluxes mediated by the activation of chloride channels associated with GABA(A receptors. Indeed through an original algorithm, chloride currents elicited by application of appropriate agonists of the GABA(A receptor can be derived from the quantitative phase signal recorded with DHM. Finally, chloride currents can be determined and pharmacologically characterized non-invasively simultaneously on a large cellular sampling by DHM.

  13. 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.

  14. 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.

  15. 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.

  16. Biomineralization of a Cadmium Chloride Nanocrystal by a Designed Symmetrical Protein.

    Science.gov (United States)

    Voet, Arnout R D; Noguchi, Hiroki; Addy, Christine; Zhang, Kam Y J; Tame, Jeremy R H

    2015-08-17

    We have engineered a metal-binding site into the novel artificial β-propeller protein Pizza. This new Pizza variant carries two nearly identical domains per polypeptide chain, and forms a trimer with three-fold symmetry. The designed single metal ion binding site lies on the symmetry axis, bonding the trimer together. Two copies of the trimer associate in the presence of cadmium chloride in solution, and very high-resolution X-ray crystallographic analysis reveals a nanocrystal of cadmium chloride, sandwiched between two trimers of the protein. This nanocrystal, containing seven cadmium ions lying in a plane and twelve interspersed chloride ions, is the smallest reported to date. Our results indicate the feasibility of using rationally designed symmetrical proteins to biomineralize nanocrystals with useful properties. PMID:26136355

  17. 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.

  18. Ionization and Dissociation of Nitrosyl Chloride Molecule in the Intense Femtosecond Laser Field

    Institute of Scientific and Technical Information of China (English)

    YAO, Li; GE, Mao-Fa; WANG, Dian-Xun; WU, Cheng-Yin; XU, Nan; GONG, Qi-Huang

    2006-01-01

    Ionization and dissociation of nitrosyl chloride ClNO were studied using femtosecond laser mass spectra technique. Strong fragmental ions NO+and Cl+were observed with the laser intensity varied from 3.2 × 1014 to 2.5 ×1015 W/cm2. These fragmental ions were attributed to the direct dissociation of the parent ions. Electronic structure calculations were also carried out with Hartree-Fock, density functional and correlated levels of theory to understand the possible fragmentation pathways. The very low N-Cl bond energy in the parent ion of nitrosyl chloride is a clear reason for the absence of ClNO+ and ClN+ ion peaks from the femtosecond laser mass spectrum.

  19. Chloride sublimation of gold-arsenic concentrates

    International Nuclear Information System (INIS)

    Present article is devoted to chloride sublimation of gold-arsenic concentrates. The results of studies of chloride sublimation of gold-arsenic comprising concentrates of Chore deposit of Tajikistan are considered. It is found that by application sodium chloride for gold-arsenic comprising concentrates it is possible to extract gold and silver from flotation concentrates.

  20. 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...

  1. 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.

  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. 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.

  4. Ion mixing, hydration, and transport in aqueous ionic systems

    International Nuclear Information System (INIS)

    The enhancement effect on the ion mobility of fluoride (and that of chloride) in a polycationic system, as the chloride content increases, is shown to also exist in other more simple ionic systems with cations such as the cesium ion and an organic ammonium ion. As the chloride content increases, in addition to the finding that there is more unbound water associated with the cation, we also observe that the average lifetime of a hydrogen bond decreases. This change to the hydrogen bonds is correlated to significant changes to both the structural and dynamical properties of water. The more disordered water structure and faster water dynamics are hypothesized to be also responsible for the enhanced ion mobilities. Furthermore, when either the chloride content or hydration level is changed, the self-diffusion constant of each co-ion changes by almost the same factor, implying the existence of a single universal transport mechanism that determines ion mobilities

  5. 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.

  6. Prediction of chloride ingress and binding in cement paste

    DEFF Research Database (Denmark)

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

    2007-01-01

    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...... 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...... profiles for the Cl/Ca ratio predicted by the model and those determined experimentally on 0.45 water/powder ratio Portland cement pastes exposed to 650 mM NaCl for 70 days. This confirms the assumption of essentially instantaneous binding where quasi-equilibrium is established locally. This does not imply...

  7. Sodium chloride's effect on self-assembly of diphenylalanine bilayer.

    Science.gov (United States)

    Kwon, Junpyo; Lee, Myeongsang; Na, Sungsoo

    2016-07-15

    Understanding self-assembling peptides becomes essential in nanotechnology, thereby providing a bottom-up method for fabrication of nanostructures. Diphenylalanine constitutes an outstanding building block that can be assembled into various nanostructures, including two-dimensional bilayers or nanotubes, exhibiting superb mechanical properties. It is known that the effect of the ions is critical in conformational and chemical interactions of bilayers or membranes. In this study, we analyzed the effect of sodium chloride on diphenylalanine bilayer using coarse-grained molecular dynamics simulations, and calculated the bending Young's modulus and the torsional modulus by applying normal modal analysis using an elastic network model. The results showed that sodium chloride dramatically increases the assembling efficiency and stability, thereby promising to allow the precise design and control of the fabrication process and properties of bio-inspired materials. © 2016 Wiley Periodicals, Inc. PMID:27241039

  8. 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.

  9. CPP-603 Chloride Removal System Decontamination and Decommissioning

    International Nuclear Information System (INIS)

    The CPP-603 (annex) Chloride Removal System (CRS) Decontamination and Decommissioning (D ampersand D) Project is described in this report. The CRS was used for removing Chloride ions and other contaminants that were suspended in the waters of the underwater fuel storage basins in the CPP-603 Fuel Receiving and Storage Facility (FRSF) from 1975 to 1981. The Environmental Checklist and related documents, facility characterization, decision analysis', and D ampersand D plans' were prepared in 1991. Physical D ampersand D activities were begun in mid summer of 1992 and were completed by the end of November 1992. All process equipment and electrical equipment were removed from the annex following accepted asbestos and radiological contamination removal practices. The D ampersand D activities were performed in a manner such that no radiological health or safety hazard to the public or to personnel at the Idaho National Engineering Laboratory (INEL) occurred

  10. Selective Measurement of Calcium and Sodium Ion Conductance Using Sub-Micropipette Probes with Ion Filters

    Science.gov (United States)

    Deng, Xiao Long; Takami, Tomohide; Son, Jong Wan; Kawai, Tomoji; Park, Bae Ho

    2012-02-01

    Selective ion currents in aqueous calcium chloride and sodium chloride solutions with concentrations of up to 1.0 M were observed with sub-micropipettes in which poly(vinyl chloride) (PVC) films containing ionophores selectively filtered cations. Calcium bis[4-(1,1,3,3-tetramethylbutyl)phenyl] phosphate (HDOPP-Ca) and bis[(12-crown-4)methyl]-2-dodecyl-2-methylmalonate [bis(12-crown-4)] were used as the ionophores to filter calcium and sodium ions, respectively. The selective ion current was observed using a low-current detection system developed from scanning tunneling microscopy. The approximate linear relationship between the ion concentration and ion current suggests that the sub-micropipette probe can be used to detect the intracellular local concentration of a specific ion up to 1.0 M.

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

    OpenAIRE

    Neeru Gupta; Kishan Kumar Jani; Nivedita Gupta

    2011-01-01

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

  12. Fabrication and Performance of All-Solid-State Chloride Sensors in Synthetic Concrete Pore Solutions

    Directory of Open Access Journals (Sweden)

    Hongwei Deng

    2010-11-01

    Full Text Available One type of all-solid-state chloride sensor was fabricated using a MnO2 electrode and a Ag/AgCl electrode. The potentiometric response of the sensor to chloride in synthetic concrete pore solutions was systematically studied, and the polarization performance was also evaluated. The results show a good linear relationship between the potential reading of the sensor and the logarithm of chloride activity (concentration ranges from 0.05 to 5.0 M, and the potential value remains stable with increasing immersion time. The existence of K+, Ca2+, Na+ and SO42− ions have little influence on the potentiometric response of the sensor to chloride, but the pH has a significant influence on the potential value of the sensor at low chloride concentration. The potential reading of the sensor increases linearly with the solution temperature over the range from 5 to 45 °C. Meanwhile, an excellent polarization behavior is proven by galvanostatic and potentiodynamic tests. All of the results reveal that the developed sensor has a great potential for monitoring chloride ions in concrete environments.

  13. Fabrication and performance of all-solid-state chloride sensors in synthetic concrete pore solutions.

    Science.gov (United States)

    Gao, Xiaojian; Zhang, Jian; Yang, Yingzi; Deng, Hongwei

    2010-01-01

    One type of all-solid-state chloride sensor was fabricated using a MnO(2) electrode and a Ag/AgCl electrode. The potentiometric response of the sensor to chloride in synthetic concrete pore solutions was systematically studied, and the polarization performance was also evaluated. The results show a good linear relationship between the potential reading of the sensor and the logarithm of chloride activity (concentration ranges from 0.05 to 5.0 M), and the potential value remains stable with increasing immersion time. The existence of K(+), Ca(2+), Na(+) and SO(4) (2-) ions have little influence on the potentiometric response of the sensor to chloride, but the pH has a significant influence on the potential value of the sensor at low chloride concentration. The potential reading of the sensor increases linearly with the solution temperature over the range from 5 to 45 °C. Meanwhile, an excellent polarization behavior is proven by galvanostatic and potentiodynamic tests. All of the results reveal that the developed sensor has a great potential for monitoring chloride ions in concrete environments. PMID:22163467

  14. A novel device for quantitative measurement of chloride concentration by fluorescence indicator

    Science.gov (United States)

    Wang, Junsheng; Wu, Xudong; Chon, Chanhee; Gonska, Tanja; Li, Dongqing

    2012-02-01

    Cystic fibrosis (CF) is a life-threatening genetic disease. At present, the common method for diagnosis of CF is to detect the chloride concentration in sweat using ion-selective electrodes. However, the current sweat testing methods require a relatively large quantity of sweat sample, at least 25 µL, which is very difficult to obtain, especially for newborns. This paper presents a new method and a new device for rapid detection of the chloride concentration from a small volume of solution. In this method, the chloride concentration is determined quantitatively by the fluorescence intensity of MQAE, a chloride ion fluorescent indicator. In this device, the sample is carried by a small piece of filter paper on a cover glass exposed to an UV LED light source. The resulting fluorescent signals are detected by a Si photodiode. Data acquisition and processing are accomplished by LabVIEW software in a PDA. Based on the Stern-Volmer relationship, the effects of different parameters on the fluorescence intensity were analyzed. The observed significant difference between 40 and 60 mM (the borderline of chloride concentration for CF) is discussed in this paper. The results show that detection can be completed within 10 s. The minimum detectable volume of the chloride solution is 1 μL. The novel method and the device are of great potential for CF diagnosis.

  15. 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.

  16. 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.

  17. 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)

  18. Corrosion Resistance of Calcium Aluminate Cement Concrete Exposed to a Chloride Environment

    Directory of Open Access Journals (Sweden)

    Ki Yong Ann

    2014-01-01

    Full Text Available The present study concerns a development of calcium aluminate cement (CAC concrete to enhance the durability against an externally chemically aggressive environment, in particular, chloride-induced corrosion. To evaluate the inhibition effect and concrete properties, CAC was partially mixed with ordinary Portland cement (OPC, ranging from 5% to 15%, as a binder. As a result, it was found that an increase in the CAC in binder resulted in a dramatic decrease in the setting time of fresh concrete. However, the compressive strength was lower, ranging about 20 MPa, while OPC indicated about 30–35 MPa at an equivalent age. When it comes to chloride transport, there was only marginal variation in the diffusivity of chloride ions. The corrosion resistance of CAC mixture was significantly enhanced: its chloride threshold level for corrosion initiation exceeded 3.0% by weight of binder, whilst OPC and CAC concrete indicated about 0.5%–1.0%.

  19. 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.

  20. 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.

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

    OpenAIRE

    Sánchez Rodríguez, Martha A; 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. 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.

  3. Crystal structure and functional characterization of a light-driven chloride pump having an NTQ motif.

    Science.gov (United States)

    Kim, Kuglae; Kwon, Soon-Kyeong; Jun, Sung-Hoon; Cha, Jeong Seok; Kim, Hoyoung; Lee, Weontae; Kim, Jihyun F; Cho, Hyun-Soo

    2016-01-01

    A novel light-driven chloride-pumping rhodopsin (ClR) containing an 'NTQ motif' in its putative ion conduction pathway has been discovered and functionally characterized in a genomic analysis study of a marine bacterium. Here we report the crystal structure of ClR from the flavobacterium Nonlabens marinus S1-08(T) determined under two conditions at 2.0 and 1.56 Å resolutions. The structures reveal two chloride-binding sites, one around the protonated Schiff base and the other on a cytoplasmic loop. We identify a '3 omega motif' formed by three non-consecutive aromatic amino acids that is correlated with the B-C loop orientation. Detailed ClR structural analyses with functional studies in E. coli reveal the chloride ion transduction pathway. Our results help understand the molecular mechanism and physiological role of ClR and provide a structural basis for optogenetic applications. PMID:27554809

  4. 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.

  5. 4-Hydroxy-1,2,6-trimethylpyridinium chloride monohydrate

    Directory of Open Access Journals (Sweden)

    T. Seethalakshmi

    2013-06-01

    Full Text Available In the crystal of the title hydrated molecular salt, C8H12NO+·Cl−·H2O, the water molecule makes two O—H...Cl hydrogen bonds, generating [010] zigzag chains of alternating water molecules and chloride ions. The cation is bonded to the chain by an O—H...O hydrogen bond and two weak C—H...Cl interactions. Weak aromatic π–π stacking [centroid–centroid separation = 3.5175 (15 Å] occurs between the chains.

  6. Electrochemical Migration on Electronic Chip Resistors in Chloride Environments

    DEFF Research Database (Denmark)

    Minzari, Daniel; Jellesen, Morten Stendahl; Møller, Per;

    2009-01-01

    Electrochemical migration behavior of end terminals on ceramic chip resistors (CCRs) was studied using a novel experimental setup in varying sodium chloride concentrations from 0 to 1000 ppm. The chip resistor used for the investigation was 10-kΩ CCR size 0805 with end terminals made of 97Sn3Pb...... alloy. Anodic polarization behavior of the electrode materials was investigated using a microelectrochemical setup. Material makeup of the chip resistor was investigated using scanning electron microscopy (SEM)/energy dispersive spectroscopy and focused-ion-beam SEM. Results showed that the dissolution...

  7. 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.

  8. 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....

  9. 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

    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....

  10. 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

  11. 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.

  12. Crevice Corrosion of 321 Stainless Steel in Sodium Chloride Solutions

    International Nuclear Information System (INIS)

    Electrochemical techniques have been applied to study the crevice corrosion behaviour of stabilized 321 stainless steel in both 0.5, 1 and 2 M sodium chloride solutions at 25 and 80 degree . This type of stainless steel enjoys a good corrosion resistance especially in the heat affected zone (Haz) of welds. In this investigation the crevice corrosion of 321 stainless steel was studied in both bulk solution environments as well as in chloride solutions simulating those formed inside crevices. A metal-to-nonmetal crevice assembly, in which disc type specimens were faced to a PTFE crevice former, is used for bulk solution tests. Crevice-free specimens of solutions formed inside crevices (known as the critical crevice solutions, CCS). Cyclic potentiodynamic technique was used in evaluating the electrochemical corrosion performance of the alloy in bulk (0.5 and 1 M Nacl) environment. This revealed that both chloride ion concentration and temperature have a marked effect on the electrochemical parameters generally used for the evaluation of the crevice corrosion susceptibility. This included the corrosion potential. E corr. The passivity breakdown potential, Eb, and the protection potential, E p

  13. Effects of concentration of sodium chloride solution on the pitting corrosion behavior of AISI 304L austenitic stainless steel

    Directory of Open Access Journals (Sweden)

    Asaduzzaman M.D.

    2011-01-01

    Full Text Available The pitting corrosion behavior of the austenitic stainless steel in aqueous chloride solution was investigated using electrochemical technique. Corrosion potential (Ecorr measurement, potentiodynamic experiments, potential-hold experiments in the passive range, and microscopic examination were used for the evaluation of corrosion characteristics. The experimental parameters were chloride ion concentration, immersion time and anodic-hold potential. Ecorr measurements along with microscopic examinations suggest that in or above 3.5 % NaCl at pH 2 pitting took place on the surface in absence of applied potential after 6 hour immersion. The potentiodynamic experiment reveals that Ecorr and pitting potential (Epit decreased and current density in the passive region increased with the increase of chloride ion concentrations. A linear relationship between Epit and chloride ion concentrations was found in this investigation. The analysis of the results suggests that six chloride ions are involved for the dissolution of iron ion in the pitting corrosion process of austenitic stainless steel.

  14. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    OpenAIRE

    H. Guan; Love, A. J.; C. T. Simmons; Makhnin, O.; A. S. Kayaalp

    2010-01-01

    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 method. A high-resolution bulk chloride deposition map in the coastal region is thus needed. The aim of this study is to construc...

  15. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    OpenAIRE

    H. Guan; Love, A. J.; C. T. Simmons; Makhnin, O.; A. S. Kayaalp

    2010-01-01

    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 method. A high-resolution bulk chloride deposition map in the coastal region is thus needed. The aim of this st...

  16. The volumetric and thermochemical properties of YCl{sub 3}(aq), YbCl{sub 3}(aq), DyCl{sub 3}(aq), SmCl{sub 3}(aq), and GdCl{sub 3}(aq) at T=(288.15, 298.15, 313.15, and 328.15) K and p=0.1 MPa[Trivalent metal chlorides; Densities; Heat capacities; Single ion properties; Calorimetry; Densimetry

    Energy Technology Data Exchange (ETDEWEB)

    Hakin, Andrew W. E-mail: hakin@uleth.ca; Lukacs, Michael J.; Liu, Jin Lian; Erickson, Kristy

    2003-11-01

    Relative densities and massic heat capacities have been measured for acidified aqueous solutions of YCl{sub 3}(aq), YbCl{sub 3}(aq), DyCl{sub 3}(aq), SmCl{sub 3}(aq), and GdCl{sub 3}(aq) at T=(288.15, 298.15, 313.15, and 328.15) K and p=0.1 MPa. These measurements have been used to calculate experimental apparent molar volumes and heat capacities which, when used in conjunction with Young's rule, were used to calculate the apparent molar properties of the aqueous chloride salt solutions. The latter calculations required the use of volumetric and thermochemical data for aqueous solutions of hydrochloric acid that have been previously reported in the literature. The concentration dependences of the apparent molar properties have been modeled using Pitzer ion interaction equations to yield apparent molar volumes and heat capacities at infinite dilution. The temperature and concentration dependences of the apparent molar volumes and heat capacities of each trivalent salt system were modeled using modified Pitzer ion interaction equations. These equations utilized the revised Helgeson, Kirkham, and Flowers equations of state to model the temperature dependences of apparent molar volumes and heat capacities at infinite dilution. Calculated apparent molar volumes and heat capacities at infinite dilution have been used to calculate single ion properties for the investigated trivalent metal cations. These values have been compared to those previously reported in the literature. The differences between single ion values calculated in this study and those values calculated from thermodynamic data for aqueous perchlorate salts are also discussed.

  17. Ameliorating Effect of Chloride on Nitrite Toxicity to Freshwater Invertebrates with Different Physiology: a Comparative Study Between Amphipods and Planarians

    OpenAIRE

    Alonso, A.; Camargo, J.A.

    2008-01-01

    High nitrite concentrations in freshwater ecosystems may cause toxicity to aquatic animals. These living organisms can take nitrite up from water through their chloride cells, subsequently suffering oxidation of their respiratory pigments (hemoglobin, hemocyanin). Because NO2¿ and Cl¿ ions compete for the same active transport site, elevated chloride concentrations in the aquatic environment have the potential of reducing nitrite toxicity. Although this ameliorating effect is well documented ...

  18. Redox reactions in rare earth chloride molten electrolytes

    International Nuclear Information System (INIS)

    Rare earth (REM, Ln) solutions in chloride melts including MCI+LnCl3 mixtures, where M - alkali metals, were investigated by potentiometry, voltammetry, conductometry in wide concentration and temperature intervals. Findings present complete and trusty information on the valent state of rare earths, structure and composition of complex ions affecting essentially on properties of electrolytes. It is demonstrated that the coexistence of rare earth ions with different oxidation level formed as a result of possible redox reactions: 2Ln3+ + Ln ↔3Ln2+, Ln2+ + Ln↔2Ln+ and nM+ + Ln↔nM + Lnn+ appears sharply in thermodynamic and transport properties of molten Ln-LnCl3 and Ln-LnCl3-MCl systems

  19. Strong and specific effects of cations on lysozyme chloride solubility.

    Science.gov (United States)

    Bénas, Philippe; Legrand, Laurent; Riès-Kautt, Madeleine

    2002-10-01

    The influence of salt nature and concentration on tetragonal lysozyme chloride crystal solubility is presented for a set of mono-, di- and trivalent cations (Cs(+), Rb(+), Mn(2+), Co(2+) and Yb(3+)). The results show that cations have as strong an effect on protein solubility as anions and that they present their own particular effects as co-ions. Indeed, after decreasing at low ionic strength, lysozyme solubility increases with high concentration of polyvalent cations, probably due to co-ion binding and therefore the concomitant increase of the net charge of the protein-salt complex. These new results are discussed in order to progress in the understanding of the crystallisation process at the atomic level. PMID:12351866

  20. 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

  1. 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)

  2. Ion-Selective Detection with Glass Nanopipette for Living Cells

    Science.gov (United States)

    Takami, T.; Son, J. W.; Kang, E. J.; Deng, X. L.; Kawai, T.; Lee, S.-W.; Park, B. H.

    2013-05-01

    We developed a method to probe local ion concentration with glass nanopipette in which poly(vinyl chloride) membrane containing ionophore for separate ion detection is prepared. Here we demonstrate how ion-selective detections are available for living cells such as HeLa cell, rat vascular myocyte, and neuron cell.

  3. 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.

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

    International Nuclear Information System (INIS)

    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)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 (Ecorr) with the corrosion current densities (icorr), 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

  5. Chloride ingress in cement paste and mortar

    DEFF Research Database (Denmark)

    Jensen, Ole Mejlhede; Hansen, Per Freiesleben; Coats, Alison M.;

    1999-01-01

    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...

  6. 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...

  7. 75 FR 19657 - Barium Chloride From China

    Science.gov (United States)

    2010-04-15

    ... Commission found that the domestic interested party group response to its notice of institution (74 FR 31757... 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...

  8. 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...

  9. 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

  10. 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.

  11. 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.

  12. Enthalpic consequences of reduced chloride binding in Andean frog (Telmatobius peruvianus) hemoglobin.

    Science.gov (United States)

    Weber, Roy E

    2014-07-01

    Based on the exothermic nature of heme oxygenation, the O2 affinity of hemoglobin (Hb) decreases with increasing temperature, which may be physiologically advantageous in augmenting O2 unloading from blood in warm tissues with elevated metabolic rates. This negative oxygenation enthalpy (∆H (O)) may, however, become maladaptive, as in cold-tolerant ungulates where it may hamper O2 unloading in cold extremities and commonly is mitigated by an 'additional' chloride-binding site that decreases the temperature effect by increasing the endothermic release of Cl(-) ions upon O2 binding. Since no previous studies have focused on the consequences of reduced Cl(-) binding, I report and compare the enthalpic effects of chloride ions and the allosteric effector, ATP, on Hbs of the high-altitude aquatic Andean frog Telmatobius peruvianus that lacks the α-chain chloride-binding site, and the lowland (sub-)tropical frog Xenopus laevis that has retained this site and exhibits high chloride sensitivity. In contrast to Xenopus, Telmatobius Hb exhibits high temperature sensitivity (high negative ∆H') in the presence of Cl(-) ions, supporting the inverse relationship between the number of Cl(-)-binding sites and temperature sensitivity, and extending it to ectothermic vertebrates. The radically reduced chloride binding in Telmatobius Hb permits assessment of the enthalpy of ATP binding [(∆H' ≈ -62 kJ (mol ATP)(-1) at pH 7.0]-which contrasts sharply with previously reported increases in temperature sensitivity by ATP in toad (Bufo bufo) Hb. The high temperature sensitivity associated with decreased chloride binding and low phosphate sensitivity of Telmatobius Hb likely promotes cutaneous O2 uptake in cold, high-altitude ponds and streams.

  13. Chloride adsorption by calcined layered double hydroxides in hardened Portland cement paste

    International Nuclear Information System (INIS)

    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. - 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

  14. 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.

  15. Electro-osmotic techniques for removal of chloride from concrete and for emplacement of concrete sealants

    Science.gov (United States)

    Jayaprakash, G. P.; Bukovatz, J. E.; Ramamurti, K.; Gilliland, W. J.

    1982-08-01

    Chloride ion from bridge deck concrete can be removed by application of a direct current potential between bridge reinforcing steel (-) and a copper screen (+) conductor on the bridge surface. Soaring prices of all types of energy would make removal of all chloride prohibitatively expensive. The importance of verification of all electrical connections prior to the treatment is emphasized by the demonstration of concrete cracking when the steel was made a positive instead of a negative electrode. Data on effectiveness of calcium nitrite corrosion inhibitor added to the concrete overlay placed on electrotreated concrete is not extensive due to accidental damage to the test slabs.

  16. 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.

  17. Shelf life of unrefrigerated succinylcholine chloride injection.

    Science.gov (United States)

    Boehm, J J; Dutton, D M; Poust, R I

    1984-02-01

    The shelf life of succinylcholine chloride injection at several pH values when stored at room temperature was evaluated. Solutions containing 20 mg/ml of succinylcholine chloride were stored at 25 and 40 degrees C. The reaction was studied at pH values ranging from 3.0 to 4.5. At two-week intervals, the solutions were assayed by high-pressure liquid chromatography. The initial amount of succinylcholine chloride in all samples was 100.1 +/- 2.37% of label claim. Hydrolysis of succinylcholine chloride in unbuffered solutions followed apparent zero-order kinetics. The pH range of maximum stability was found to be from 3.75 to 4.50. Succinylcholine chloride decomposed at a considerably higher rate at 40 degrees C. Allowing for the effects of pH adjustment during manufacture and degradation during shipping, losses of 7.0% and 9.0% potency can be expected after storage at 25 degrees C for four and six weeks, respectively. Succinylcholine Chloride Injection, USP, should be stored in the refrigerator; if unbuffered succinylcholine chloride injection complying with USP pH limits must be stored at room temperature, it should not be kept for longer than four weeks. PMID:6702837

  18. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    Directory of Open Access Journals (Sweden)

    H. Guan

    2010-05-01

    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 method. A high-resolution bulk chloride deposition map in the coastal region is thus needed. The aim of this study is to construct a chloride deposition map in the Mount Lofty Ranges (MLR, a coastal hilly area of approximately 9000 km2 spatial extent in South Australia. We examined geographic (related to coastal distance, orographic, and atmospheric factors that may influence chloride deposition, using partial correlation and regression analyses. The results indicate that coastal distance, elevation, as well as terrain aspect and slope, appear to be significant factors controlling chloride deposition in the study area. Coastal distance accounts for 70% of spatial variability in bulk chloride deposition, with elevation, terrain aspect and slope an additional 15%. The results are incorporated into a de-trended residual kriging model (ASOADeK to produce a 1 km×1 km resolution bulk chloride deposition and concentration maps. The average uncertainty of the deposition map is about 20–30% in the western MLR, and 40–50% in the eastern MLR. The maps will form a useful basis for examining catchment chloride balance for the CMB application in the study area.

  19. Chloride channels in toad skin

    DEFF Research Database (Denmark)

    Larsen, Erik Hviid; Rasmussen, B E

    1982-01-01

    - ions through this pathway. Experimental analysis of the gating kinetics is rendered difficult owing to a contamination of the gated currents by cellular ion redistribution currents. To obtain insight into the effects of accumulation-depletion currents on voltage clamp currents of epithelial membranes......, a mathematical model of the epithelium has been developed for computer analysis. By assuming that the apical membrane Cl- permeability is governed by a single gating variable (Hodgkin-Huxley kinetics), the model predicts fairly well steady-state current-voltage curves, the time course of current activations from...... a closed state, and the dependence of unidirectional fluxes on potential. Other predictions of the model do not agree with experimental findings, and it is suggested that the gating kinetics are governed by rate coefficients that also depend on the holding potential. Evidence is presented that Cl...

  20. 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...

  1. Binary Nucleation of Water and Sodium Chloride

    Energy Technology Data Exchange (ETDEWEB)

    Nemec, Thomas [Institute of Thermomechanics ASCR, Prague, Czech Republic; Marsik, Frantisek [Institute of Thermomechanics ASCR, Prague, Czech Republic; Palmer, Donald [ORNL

    2005-01-01

    Nucleation processes in the binary water-sodium chloride system are investigated in the sense of the classical nucleation theory (CNT). The CNT is modified to be able to handle the electrolytic nature of the system and is employed to investigate the acceleration of the nucleation process due to the presence of sodium chloride in the steam. This phenomenon, frequently observed in the Wilson zone of steam turbines, is called early condensation. Therefore, the nucleation rates of the water-sodium chloride mixture are of key importance in the power cycle industry.

  2. 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)

  3. 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

  4. 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.

  5. 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.

  6. The evaluation of organic inhibitors for the protection of grade 5 titanium in chloride media

    International Nuclear Information System (INIS)

    The corrosion failures of titanium and titanium alloys are inevitably associated with the non-observance of environmental limits prescribed in corrosion handbooks, such as its use in solutions chloride. Titanium alloys are often used in the thermal transfer technology especially in the heat exchangers cooled with sea cooled water. However, it is not indicated its use in strong oxidant and any concentrated chloride environments. For the evaluation of grade 5 titanium alloy samples behaviour in solutions containing chloride ions in presence, respectively, absence of some organic inhibitors were performed by potentiodynamic polarization method. On the basis of our experimental results we consider that the most adequate inhibitor for the system Ti-5 alloys/0.083M NaCl solution is the resorcinol. (authors)

  7. 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...

  8. 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.

  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. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    OpenAIRE

    H. Guan; Love, A. J.; C. T. Simmons; A. S. Kayaalp

    2009-01-01

    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...

  11. 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}.

  12. 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.

  13. Lysozyme net charge and ion binding in concentrated aqueous electrolyte solutions

    Energy Technology Data Exchange (ETDEWEB)

    Kuehner, Daniel E.; Engmann, Jan; Fergg, Florian; Wernick, Meredith; Blanch, Harvey W. [Univ. of California, Berkeley, CA (United States). Dept. of Chemical Engineering; Prausnitz, John M. [Univ. of California, Berkeley, CA (United States). Dept. of Chemical Engineering

    1999-02-01

    Hydrogen-ion titrations were conducted for hen-egg-white lysozyme in solutions of potassium chloride over the range pH 2.5--11.5 and for ionic strengths to 2.0 M. The dependence of lysozyme`s net proton charge, z{sub p}, on pH and ionic strength in potassium chloride solution is measured. From the ionic-strength dependence of z{sub p}, interactions of lysozyme with potassium and chloride ions are calculated using the molecular-thermodynamic theory of Fraaije and Lyklema. Lysozyme interacts preferentially with up to 12 chloride ions at pH 2.5. The observed dependence of ion-protein interactions on pH and ionic strength is explained in terms of electric-double-layer theory. New experimental pK{sub a} data are reported for 11 amino acids in potassium chloride solutions of ionic strength to 3.0 M.

  14. 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.

  15. 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. PMID:18471966

  16. 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.

  17. Inhibition of herpes simplex virus type 1 entry by chloride channel inhibitors tamoxifen and NPPB

    International Nuclear Information System (INIS)

    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

  18. 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.

  19. 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.

  20. 21 CFR 178.3290 - Chromic chloride complexes.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Chromic chloride complexes. 178.3290 Section 178... SANITIZERS Certain Adjuvants and Production Aids § 178.3290 Chromic chloride complexes. Myristo chromic chloride complex and stearato chromic chloride complex may be safely used as release agents in the...

  1. 49 CFR 179.102-17 - Hydrogen chloride, refrigerated liquid.

    Science.gov (United States)

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Hydrogen chloride, refrigerated liquid. 179.102-17...) § 179.102-17 Hydrogen chloride, refrigerated liquid. Each tank car used to transport hydrogen chloride... on or after March 16, 2009 used for the transportation of hydrogen chloride, refrigerated...

  2. 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.)

  3. Effects of pH and chloride concentration on pitting corrosion of AA6061 aluminum alloy

    Energy Technology Data Exchange (ETDEWEB)

    Zaid, B. [Division de Technologie du Combustible, Departement de Metallurgie, Centre de Recherche Nucleaire de Draria, BP. 43 Seballa, Draria (Algeria)], E-mail: zaidbachir@yahoo.com; Saidi, D. [Division de Technologie du Combustible, Departement de Metallurgie, Centre de Recherche Nucleaire de Draria, BP. 43 Seballa, Draria (Algeria); Benzaid, A. [Divisionde Physique et Application Nucleaires, Departement Application Nucleaires, Centre de Recherche Nucleaire de Draria, BP. 43 Seballa, Draria (Algeria); Hadji, S. [Division de Technologie du Combustible, Departement du combustible, Centre de Recherche Nucleaire de Draria, BP. 43 Seballa, Draria (Algeria)

    2008-07-15

    Effects of pH solution and chloride (Cl{sup -}) ion concentration on the corrosion behaviour of alloy AA6061 immersed in aqueous solutions of NaCl have been investigated using measurements of weight loss, potentiodynamic polarisation, linear polarisation, cyclic polarisation experiment combined with open circuit potential transient technique and optical or scanning electron microscopy. The corrosion behaviour of the AA6061 aluminum alloy was found to be dependant on the pH and chloride concentration [NaCl] of solution. In acidic or slightly neutral solutions, general and pitting corrosion occurred simultaneously. In contrast, exposure to alkaline solutions results in general corrosion. Experience revealed that the alloy AA6061 was susceptible to pitting corrosion in all chloride solution of concentration ranging between 0.003 wt% and 5.5 wt% NaCl and an increase in the chloride concentration slightly shifted both the pitting E{sub pit} and corrosion E{sub cor} potentials to more active values. In function of the conditions of treatment, the sheets of the alloy AA6061 undergo two types of localised corrosion process, leading to the formation of hemispherical and crystallographic pits. Polarisation resistance measurements in acidic (pH = 2) and alkaline chloride solutions (pH = 12) which are in good agreement with those of weight loss, show that the corrosion kinetic is minimised in slightly neutral solutions (pH = 6)

  4. GmCLC1 Confers Enhanced Salt Tolerance through Regulating Chloride Accumulation in Soybean.

    Science.gov (United States)

    Wei, Peipei; Wang, Longchao; Liu, Ailin; Yu, Bingjun; Lam, Hon-Ming

    2016-01-01

    The family of chloride channel proteins that mediate Cl(-) transportation play vital roles in plant nutrient supply, cellular action potential and turgor pressure adjustment, stomatal movement, hormone signal recognition and transduction, Cl(-) homeostasis, and abiotic and biotic stress tolerance. The anionic toxicity, mainly caused by chloride ions (Cl(-)), on plants under salt stress remains poorly understood. In this work, we investigated the function of soybean Cl(-)/H(+) antiporter GmCLC1 under salt stress in transgenic Arabidopsis thaliana, soybean, and yeast. We found that GmCLC1 enhanced salt tolerance in transgenic A. thaliana by reducing the Cl(-) accumulation in shoots and hence released the negative impact of salt stress on plant growth. Overexpression of GmCLC1 in the hairy roots of soybean sequestered more Cl(-) in their roots and transferred less Cl(-) to their shoots, leading to lower relative electrolyte leakage values in the roots and leaves. When either the soybean GmCLC1 or the yeast chloride transporter gene, GEF1, was transformed into the yeast gef1 mutant, and then treated with different chloride salts (MnCl2, KCl, NaCl), enhanced survival rate was observed. The result indicates that GmCLC1 and GEF1 exerted similar effects on alleviating the stress of diverse chloride salts on the yeast gef1 mutant. Together, this work suggests a protective function of GmCLC1 under Cl(-) stress. PMID:27504114

  5. A Thermo-Hygro-Coupled Model for Chloride Penetration in Concrete Structures

    Directory of Open Access Journals (Sweden)

    Nattapong Damrongwiriyanupap

    2015-01-01

    Full Text Available Corrosion damage due to chloride attack is one of the most concerning issues for long term durability of reinforced concrete structures. By developing the reliable mathematical model of chloride penetration into concrete structures, it can help structural engineers and management agencies with predicting the service life of reinforced concrete structures in order to effectively schedule the maintenance, repair, and rehabilitation program. This paper presents a theoretical and computational model for chloride diffusion in concrete structures. The governing equations are taking into account the coupled transport process of chloride ions, moisture, and temperature. This represents the actual condition of concrete structures which are always found in nonsaturated and nonisothermal conditions. The fully coupled effects among chloride, moisture, and heat diffusion are considered and included in the model. The coupling parameters evaluated based on the available material models and test data are proposed and explicitly incorporated in the governing equations. The numerical analysis of coupled transport equations is performed using the finite element method. The model is validated by comparing the numerical results against the available experimental data and a good agreement is observed.

  6. Synthesis and characterization of zinc chloride containing poly(acrylic acid) hydrogel by gamma irradiation

    International Nuclear Information System (INIS)

    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. - Highlights: • The characterization of zinc chloride containing PAA hydrogel was investigated. • The gel content increased with an increase in absorbed dose up to 75 kGy. • Finally, the zinc chloride based hydrogels have an antibacterial activity

  7. 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.

  8. 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.

  9. 单硫型水化硫铝酸钙对氯离子的固化作用%Chloride Binding in Monosulfoaluminate Hydrate

    Institute of Scientific and Technical Information of China (English)

    勾密峰; 管学茂; 张海波

    2012-01-01

    通过化学分析法、X射线衍射法(XRD)研究了侵蚀液的浓度、溶液组成、温度对单硫型水化硫铝酸钙固化氯离子的影响.结果表明:单硫型水化硫铝酸钙固化氯离子的关系适合Freundlich 非线性关系;单硫型水化硫铝酸钙对氯离子的固化是通过氯离子与硫酸根的离子交换作用生成了Friedel盐而成;与钠离子相比,侵蚀液中的钙离子能增加单硫型水化硫铝酸钙固化氯离子的能力;随着温度的升高,单硫型水化硫铝酸钙固化氯离子的能力降低.%Chloride binding in cement can reduce the risk of steel corrosion of concrete. The influence of chloride concentration, composition of corrosion solution, temperature on chloride binding in monosulfoaluminate hydrate was investigated by analytical methods including X-ray diffraction. The results show that the binding relationships between free and bound chloride can be described by the Freundlich isotherm. Chloride binding of monosulfoaluminate hydrate is attributed to the formation of Friedel's salt through ions exchange of chloride ions and sulfate ions. Calcium ions of corrosion solution can increase chloride binding capacity in monosulfoaluminate hydrate comparing with sodium ions. The chloride binding ability in monosulfoaluminate hydrate reduces with rise of temperature.

  10. 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.

  11. 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.

  12. 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).

  13. 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.

  14. 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.

  15. 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

  16. Experimental Investigation on Pore Structure Characterization of Concrete Exposed to Water and Chlorides

    OpenAIRE

    Jun Liu; Kaifeng Tang; Qiwen Qiu; Dong Pan; Zongru Lei; Feng Xing

    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...

  17. 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...

  18. A cyclic GMP-dependent calcium-activated chloride current in smooth-muscle cells from rat mesenteric resistance arteries

    DEFF Research Database (Denmark)

    Matchkov, Vladimir; Aalkjær, Christian; Nilsson, Holger

    2004-01-01

    differed from those of the calcium-activated chloride current in pulmonary myocytes, which was cGMP-independent, exhibited a high sensitivity to inhibition by niflumic acid, was unaffected by zinc ions, and showed outward current rectification as has previously been reported for this current. Under...

  19. 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.

  20. Interlayer interaction in Ca-Fe layered double hydroxides intercalated with nitrate and chloride species

    Science.gov (United States)

    Al-Jaberi, Muayad; Naille, Sébastien; Dossot, Manuel; Ruby, Christian

    2015-12-01

    Ca-Fe layered double hydroxide (LDH) intercalated with chloride and nitrate ions has been synthesized with varying CaII:FeIII molar ratios of the initial solution. Phase pure LDH is observed with CaII:FeIII molar ratio of 2:1 and a mixture of LDH and Ca(OH)2 is formed for CaII:FeIII molar ratios higher than 2:1. Vibrational spectroscopies (Raman and IR) were used successfully to understand the interaction between the cationic and anionic sheets. The Raman bands positions at lower frequencies (150-600 cm-1) are intimately correlated to the nature of the divalent and trivalent ions but also to the nature of the anions. Indeed, a shift of ˜9 cm-1 is observed for the Raman double bands situated in the 300-400 cm-1 region when comparing Raman spectra of CaFe-LDH containing either nitrate or chloride ions. Two types of nitrate environments are observed namely free (non-hydrogen bonded) nitrate and nitrate hydrogen bonded to the interlayer water or to the 'brucite-like' hydroxyl surface. Multiple types of water structure are observed and would result from different hydrogen bond structures. Water bending modes are identified at 1645 cm-1 greater than the one observed for LDH intercalated with chloride anions (1618 cm-1), indicating that the water is strongly hydrogen bonded to the nitrate anions.

  1. 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.

  2. Differentiation of energy expenditure of membrane electrochemical utilization of lithium chloride in polymeric fibers production

    International Nuclear Information System (INIS)

    Electric power consumption for preparation of lithium hydroxide aqueous solution for regeneration stage in production of polymer fibers in a wide range of catholyte volumetric consumption has been calculated by the data of laboratory experiments, the results are presented. Energy consumption for lithium ions transfer through the Nafion membrane has been separated. It is shown that under stationary conditions of lithium chloride aqueous solution electrolysis and at current loading on the membrane approximately up to 1 kA x m-2 the drifting lithium ions can not upset preliminary flooding of the membrane. 10 refs.; 3 figs.; 1 tab

  3. Ion exchange purification of scandium

    Science.gov (United States)

    Herchenroeder, Laurie A.; Burkholder, Harvey R.

    1990-10-23

    An improvement in purification of scandium through ion exchange chromatography is disclosed in which the oxidation potential of the eluting solution is altered by the addition of potassium chlorate or ammonium chloride so that removal of contaminants is encouraged. The temperature, pH and concentration of the eluent HEDTA are controlled in order to maintain the scandium in the column while minimizing dilution of the scandium band. Recovery of scandium is improved by pumping dilute scandium over the column prior to stripping the scandium and precipitation. This eliminates the HEDTA ion and other monovalent cations contaminating the scandium band. This method maximizes recovery of scandium while maintaining purity.

  4. 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).

  5. 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.

  6. 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.

  7. 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.

  8. Interaction and conformational changes of chromatin with divalent ions.

    OpenAIRE

    Borochov, N; Ausio, J; Eisenberg, H

    1984-01-01

    We have investigated the interaction of divalent ions with chromatin towards a closer understanding of the role of metal ions in the cell nucleus. The first row transition metal ion chlorides MnCl2, CoCl2, NiCl2 and CuCl2 lead to precipitation of chicken erythrocyte chromatin at a significantly lower concentration than the alkali earth metal chlorides MgCl2, CaCl2 and BaCl2. A similar distinction can be made for the compaction of chromatin to the "30 nm" solenoid higher order structure which ...

  9. 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.

  10. Fluid shear stress enhances the cell volume decrease of osteoblast cells by increasing the expression of the ClC-3 chloride channel

    OpenAIRE

    Liu, Li; Cai, Siyi; Qiu, Guixing; Lin, Jin

    2016-01-01

    ClC-3 is a volume-sensitive chloride channel that is responsible for cell volume adjustment and regulatory cell volume decrease (RVD). In order to evaluate the effects of fluid shear stress (FSS) stimulation on the osteoblast ClC-3 chloride channel, MC3T3-E1 cells were stimulated by FSS in the experimental group. Fluorescence quantitative polymerase chain reaction was used to detect changes in ClC-3 mRNA expression, the chloride ion fluorescent probe N-(ethoxycarbonylmethyl)-6-methoxyquinolin...

  11. Method for preparation of melts of alkali metal chlorides with highly volatile polyvalent metal chlorides

    International Nuclear Information System (INIS)

    A method for production of alkali metal (Cs, Rb, K) chloride melts with highly volatile polyvalent metal chlorides is suggested. The method consists, in saturation of alkali metal chlorides, preheated to the melting point, by volatile component vapours (titanium tetrachloride, molybdenum or tantalum pentachloride) in proportion, corresponding to the composition reguired. The saturation is realized in an evacuated vessel with two heating areas for 1-1.5 h. After gradual levelling of temperature in both areas the product is rapidly cooled. 1 fig.; 1 tab

  12. 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.

  13. 75 FR 20625 - Barium Chloride From China

    Science.gov (United States)

    2010-04-20

    ... established a schedule for the conduct of this review (74 FR 62587, November 30, 2010). Subsequently, counsel... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE COMMISSION Barium Chloride From China AGENCY: United States International Trade Commission. ACTION:...

  14. 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...

  15. Determination of chloride in uranium solutions

    Energy Technology Data Exchange (ETDEWEB)

    Danse, A.; Stoch, H.; Steele, T.W.

    1967-05-15

    Thiocyanate is first removed by precipitation with a small excess of a copper solution, and the cations are removed by passing the filtrate through a cation-exchange resin. The chloride is determined in the eluate by a potentiometric titration in which silver nitrate solution is used.

  16. 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

  17. 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 §...

  18. Simulation of specific conductance and chloride concentration in Abercorn Creek, Georgia, 2000-2009

    Science.gov (United States)

    Conrads, Paul A.; Roehl, Edwin A.; Davie, Steven R.

    2011-01-01

    The City of Savannah operates an industrial and domestic water-supply intake on Abercorn Creek approximately 2 miles from the confluence with the Savannah River upstream from the Interstate 95 bridge. Chloride concentrations are a major concern for the city because industrial customers require water with low chloride concentrations, and elevated chloride concentrations require additional water treatment in order to meet those needs. The proposed deepening of Savannah Harbor could increase chloride concentrations (the major ion in seawater) in the upper reaches of the lower Savannah River estuary, including Abercorn Creek. To address this concern, mechanistic and empirical modeling approaches were used to simulate chloride concentrations at the city's intake to evaluate potential effects from deepening the Savannah Harbor. The first approach modified the mechanistic Environmental Fluid Dynamics Code (EFDC) model developed by Tetra Tech and used for evaluating proposed harbor deepening effects for the Environmental Impact Statement. Chloride concentrations were modeled directly with the EFDC model as a conservative tracer. This effort was done by Tetra Tech under a separate funding agreement with the U.S. Army Corps of Engineers and documented in a separate report. The second approach, described in this report, was to simulate chloride concentrations by developing empirical models from the available data using artificial neural network (ANN) and linear regression models. The empirical models used daily streamflow, specific conductance (field measurement for salinity), water temperature, and water color time series for inputs. Because there are only a few data points that describe the relation between high specific conductance values at the Savannah River at Interstate 95 and the water plant intake, there was a concern that these few data points would determine the extrapolation of the empirical model and potentially underestimate the effect of deepening the harbor on

  19. 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.

  20. 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.

  1. 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.

  2. A cytochemical study of the "chloride cells" in the skin of a fresh-water teleost (Channa striata (Bl.) Channidae, Pisces).

    Science.gov (United States)

    Banerjee, T K; Mittal, A K

    1975-01-01

    The chloride cells in the skin of Channa striata have been described. The cytoplasm of these cells is filled with acidophilic, osmiophilic and sudanophilic granules. The sudanophila is due to phospholipids. These cells give positive reaction for chloride ions and exhibit the presence of neutral mucopolysaccharides. The cytoplasm of these cells is packed with numerous mitochondria and exhibit high succinic dehydrogenase activity which may provide the energy needed for the active transportation of ions. Alkaline phosphatase activity could not be demonstrated in these cells. The presence of chloride cells in comparatively large numbers in the regions where the epidermis is thin is correlated as an adaptation for the increased efficiency of these cells for the transportation of ions so as to maintain the osmotic concentration of its body fluid which is higher than that of the surrounding medium. PMID:127502

  3. 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

  4. [Sweat chloride measurement using direct potentiometry: Spotchem(®) (Elitech-Arkray) evaluation and comparison with coulometry and conductivity].

    Science.gov (United States)

    Nguyen-Khoa, Thao; Borgard, Jean-Pierre; Miled, Ryad; Rota, Michèle

    2013-01-01

    Sweat chloride (Cl(-)) measurement is a key step for the diagnosis of cystic fibrosis. The coulometric technique is validated in this context by international guidelines. The aim of our study was to evaluate the assay for sweat Cl(-) ions using direct potentiometry on disposable cassette (Spotchem™ SE EL-1520, Elitech-Arkray) by comparing results to those obtained on the same sample, by coulometry (Chloride analyser Sherwood 926S, Dutscher). To complete our table of correspondence between the results of Cl(-) ions and sweat conductivity (Sweat Check™ 3100), conductivity has been also achieved for 99 of the 139 sweat samples studied. Linearity of each technique performed extends from 10 to 120 mmol/L. The coefficients of variation within and between runs are Spotchem] = 1.026 [Chloride analyser] + 1.8, r = 0.996. After correction with regression factors, only 6 pairs of values (4.6%) had a difference greater than ± 5 mmol/L). The results of conductivity measurement is strongly correlated with those of Cl(-) ions (r = 0.959 for Chloride analyser and 0.965 for Spotchem; p = 0.576) with a linear relationship between the decision thresholds from 30 to 60 mmol/L Cl(-). Sweat Cl(-) determinations using Spotchem™ analyser meet the criteria required by analytical recommendations. The technique is standardized, easy to perform and fast. Its good practicability makes the sweat test independent to operator and allows point-of care use. PMID:23906572

  5. 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)

  6. 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....... The performance loss was recovered when switching from the HCl solution back to pure water in the air humidifier. Under an accelerated aging performance test conducted through potential cycling between 0.9 V and 1.2 V, the PBI-based fuel cell initially containing 0.5 NaCl mg cm−2 on the cathode catalyst layer...

  7. (η6-Benzene)(2,2′-bipyridine-κ2 N,N′)chloridoruthenium(II) chloride methanol sesquisolvate

    OpenAIRE

    Polson, Matthew I. J.

    2007-01-01

    In the title compound, [RuCl(C6H6)(C10H8N2)]Cl·1.5CH4O, the RuII atom is in a distorted octahedral environment coordinated by an η6-benzene ring, a chelating 2,2′-bipyridine ligand and a chloride ion. The asymmetric unit is completed by a chloride anion and two methanol molecules, one of which is disordered about a centre of inversion with an occupancy of 0.5. It is an example of a ruthenium complex with a less sterically congested environment than in similar derivatives. In t...

  8. 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.

  9. Direct versus indirect electrochemical oxidation of pesticide polluted drainage water containing sodium chloride

    DEFF Research Database (Denmark)

    Muff, Jens; Erichsen, Rasmus; Damgaard, Christian;

    2008-01-01

    Drainage water from a depot of chemical waste, polluted with a mixture of organophosphates and degradation products was treated by a direct as well as an indirect electrochemical method using a Ti/Pt-Ir anode and Stainless Steel 304 cathode. With a concentration of 0.7%, sodium chloride was the m......Drainage water from a depot of chemical waste, polluted with a mixture of organophosphates and degradation products was treated by a direct as well as an indirect electrochemical method using a Ti/Pt-Ir anode and Stainless Steel 304 cathode. With a concentration of 0.7%, sodium chloride....... The experiments proved that the obtained degradation of pesticide solely was caused by indirect electrochemical oxidation, mainly due to the electrolytic formation of hypochlorite during the treatment, and that direct electron transfer from the pesticide substances at the anode surface didn't significantly...... to electrolytic oxidation of chloride with subsequent indirect oxidation by hypochlorite due to the high impact of the electric field on the chloride ion. In this way, the theoretical calculations supported the experimental results....

  10. Chloride secretagogues stimulate inositol phosphate formation in shark rectal gland tubules cultured in suspension

    Energy Technology Data Exchange (ETDEWEB)

    Ecay, T.W.; Valentich, J.D. (Univ. of Texas Medical School, Houston (USA))

    1991-03-01

    Neuroendocrine activation of transepithelial chloride secretion by shark rectal gland cells is associated with increases in cellular cAMP, cGMP, and free calcium concentrations. We report here on the effects of several chloride secretagogues on inositol phosphate formation in cultured rectal gland tubules. Vasoactive intestinal peptide (VIP), atriopeptin (AP), and ionomycin increase the total inositol phosphate levels of cultured tubules, as measured by ion exchange chromatography. Forskolin, a potent chloride secretagogue, has no effect on inositol phosphate formation. The uptake of {sup 3}H-myo-inositol into phospholipids is very slow, preventing the detection of increased levels of inositol trisphosphate. However, significant increases in inositol monophosphate (IP1) and inositol biphosphate (IP2) were measured. The time course of VIP- and AP-stimulated IP1 and IP2 formation is similar to the effects of these agents on the short-circuit current responses of rectal gland monolayer cultures. In addition, aluminum fluoride, an artificial activator of guanine nucleotide-binding proteins, stimulates IP1 and IP2 formation. We conclude that rectal gland cells contain VIP and AP receptors coupled to the activation of phospholipase C. Coupling may be mediated by G-proteins. Receptor-stimulated increases in inositol phospholipid metabolism is one mechanism leading to increased intracellular free calcium concentrations, an important regulatory event in the activation of transepithelial chloride secretion by shark rectal gland epithelial cells.

  11. 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.

  12. 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.

  13. Removal of iron contaminant from zirconium chloride solution

    International Nuclear Information System (INIS)

    This patent describes a process for eliminating iron contaminant from an aqueous zirconium chloride solution that has been contaminated with FeCl3 in a plant in which zirconium and hafnium chloride solutions are separated by a main MINK solvent extraction system and the FeCl3 is normally removed from the zirconium chloride solution by a secondary MINK solvent extraction system

  14. 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.

  15. Crystal structure and functional characterization of a light-driven chloride pump having an NTQ motif

    Science.gov (United States)

    Kim, Kuglae; Kwon, Soon-Kyeong; Jun, Sung-Hoon; Cha, Jeong Seok; Kim, Hoyoung; Lee, Weontae; Kim, Jihyun F.; Cho, Hyun-Soo

    2016-01-01

    A novel light-driven chloride-pumping rhodopsin (ClR) containing an ‘NTQ motif' in its putative ion conduction pathway has been discovered and functionally characterized in a genomic analysis study of a marine bacterium. Here we report the crystal structure of ClR from the flavobacterium Nonlabens marinus S1-08T determined under two conditions at 2.0 and 1.56 Å resolutions. The structures reveal two chloride-binding sites, one around the protonated Schiff base and the other on a cytoplasmic loop. We identify a ‘3 omega motif' formed by three non-consecutive aromatic amino acids that is correlated with the B–C loop orientation. Detailed ClR structural analyses with functional studies in E. coli reveal the chloride ion transduction pathway. Our results help understand the molecular mechanism and physiological role of ClR and provide a structural basis for optogenetic applications. PMID:27554809

  16. Revised Model of Chloride Diffusion in Concrete Bridge by Considering Complex Action of Load and Chloride Binding Capacity

    OpenAIRE

    Xiang, Yiqiang; Guo, DongMei

    2014-01-01

    Coastal concrete bridges will suffer from deterioration of RC structural performance and resistance attenuation because of the chloride penetration and other environment factors. This article discusses current different chloride diffusion models and puts forward the revised model of chloride diffusion in concrete bridge by considering the complex action of load influence and chloride-binding capacity. Comparison of numerical predicted values and relative experimental tests show the presented ...

  17. Liquid-Liquid Extraction and Separation of Co (II) and Ni(II) from Chloride Medium by bis (2,4,4-trimethylpentyl) dithio phosphinic acid in Kerosene

    International Nuclear Information System (INIS)

    The extraction of Co(II) and Ni(II) from chloride solutions using bis (2,4,4-trimethylpentyl) dithio phosphinic acid (CYANEX 301) in kerosene has been investigated. The various factors affecting the extraction process of Co(II) and Ni(II) by the investigated extractant such as contact time, ph, extractant and metal ion concentration as well as temperature, are separately investigated. The stripping of the extracted metal ions from loaded organic solutions is also carried out using different stripping reagents. The results were used to assess the conditions for maximum Co(II)/Ni(II) separation from chloride medium using CYANEX 301

  18. cis-Aqua­chloridobis(1,10-phenanthroline-κ2 N,N′)cobalt(II) chloride 2.5-hydrate

    OpenAIRE

    K. Arun Kumar; Dayalan, A.; Sethusankar, K.

    2009-01-01

    In the title complex, [CoCl(C12H8N2)2(H2O)]Cl·2.5H2O, the CoII ion is coordinated by four N atoms of two bis-chelating 1,10-phenanthroline (phen) ligands, one water molecule and a chloride ligand in a distorted octahedral environment. The dihedral angle between the two phen ligands is 84.21 (3)°. In the crystal structure, complex molecules and chloride ions are linked into centrosymmetric four-component clusters by intermolecular O—H...Cl hydrogen bonds. ...

  19. 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

  20. Activity coefficients in (hydrogen chloride+holmium chloride) (aq) from T=(278.15 to 328.15) K

    International Nuclear Information System (INIS)

    Activity coefficients of HCl in (hydrogen chloride+holmium chloride) (aq) have been calculated from the observed e.m.f.s using the Nernst equation. The temperatures ranged from (278.15 to 328.15) K at 5 K intervals and at constant total ionic strengths of (0.01, 0.025, 0.05, 0.1, 0.25, 0.5, 1.0, and 1.5) mol.kg-1. Electromotive-force measurements were made on the cell without liquid junction of the type:Pt vertical bar H2(g,p=101.325kPa) vertical bar HCl(mA),HoCl3(mB) vertical bar AgCl(s), vertical bar Ag(s) The results of the activity coefficients of HCl for this mixed electrolyte mixture have been interpreted in terms of the simpler Harned's equations and the ion-interaction model of Pitzer. Results show that the quadratic term is sufficient for the full range of YB (the ionic strength fraction of the salt) to 0.9 at all the ionic strengths studied. The Pitzer's mixing parameters SθH,Ho and ΨH,Ho,Cl (including higher order electrostatic effects) and θH,Ho and ΨH,Ho,Cl (excluding higher order electrostatic effects) have been determined. These values at T=298.15 K are: SθH,Ho=0.115, ΨH,Ho,Cl=-.071; and θH,Ho=-.663, ΨH,Ho,Cl=0.165. The parameters obtained in this study reproduce the activity coefficients of HCl in the mixtures within 0.015 over the entire range of ionic strengths and within 0.009 for I>=0.05 mol.kg-1 over the entire temperature range

  1. 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.

  2. 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.

  3. Chloride migration in concrete with superabsorbent polymers

    OpenAIRE

    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 mixtures aretested 7, 14, and 28 days after casting. The development of degree of hydration is followed for 20 corresponding paste mixtures.Both when SAP is added with extra water to compensate the SAP wa...

  4. A Duplex Stainless Steel for Chloride Environments

    Science.gov (United States)

    Sridhar, N.; Kolts, J.; Flasche, L. H.

    1985-03-01

    This paper examines the effects of microstructural changes on the corrosion, stress corrosion cracking and corrosion fatigue resistance of a duplex stainless steel to chloride environments. The microstructural changes can be precipitation of phases such as sigma and carbides, or changes in the distribution of austenite and ferrite. The former can be important in hot forming operations while the latter is important in welding. The methods of minimizing these deleterious effects can sometimes be different from those used for austenitic stainless steel.

  5. Electrodeposition of Zinc from Chloride Solution

    OpenAIRE

    NAIK, Yanjerappa Arthoba; VENKATESHA, Thimmappa Venkatarangaiah

    2002-01-01

    The electroplating of zinc is carried out in the presence of 3,4,5-Trimethoxy benzaldehyde from a chloride bath. The bath constituents are optimized through Hull cell experiments. Operating parameters such as pH, temperature, and current density are also optimized. The current efficiency and throwing power are measured at different current densities. Polarization study is carried out under galvanostatic conditions. Corrosion resistance test indicated good protection of steel by the ...

  6. 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.

  7. 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.

  8. An autopsy case of zinc chloride poisoning.

    Science.gov (United States)

    Kondo, Takeshi; Takahashi, Motonori; Watanabe, Seiya; Ebina, Masatomo; Mizu, Daisuke; Ariyoshi, Koichi; Asano, Migiwa; Nagasaki, Yasushi; Ueno, Yasuhiro

    2016-07-01

    Ingestion of large amounts of zinc chloride causes corrosive gastroenteritis with vomiting, abdominal pain, and diarrhea. Some individuals experience shock after ingesting large amounts of zinc chloride, resulting in fatality. Here, we present the results of an administrative autopsy performed on a 70-year-old man who ingested zinc chloride solution and died. After drinking the solution, he developed vomiting, abdominal pain, and diarrhea, and called for an ambulance. Except for tachycardia, his vital signs were stable at presentation. However, he developed hypotension and severe metabolic acidosis and died. The patient's blood zinc concentration on arrival was high at 3030μg/dL. Liver cirrhosis with cloudy yellow ascites was observed, however, there were no clear findings of gastrointestinal perforation. The gastric mucosa was gray-brown, with sclerosis present in all gastric wall layers. Zinc staining was strongly positive in all layers. There was almost no postmortem degeneration of the gastric mucosal epithelium, and hypercontracture of the smooth muscle layer was observed. Measurement of the zinc concentration in the organs revealed the highest concentration in the gastric mucosa, followed by the pancreas and spleen. Clinically, corrosive gastroenteritis was the cause of death. However, although autopsy revealed solidification in the esophagus and gastric mucosa, there were no findings in the small or large intestine. Therefore, metabolic acidosis resulting from organ damage was the direct cause of death. PMID:27497327

  9. 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.

  10. 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...

  11. 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.

  12. [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.

  13. Influence of temporal resolution and processing of exposure data on modeling of chloride ingress and reinforcement corrosion in concrete

    DEFF Research Database (Denmark)

    Flint, Madeleine; Michel, Alexander; Billington, Sarah L.;

    2014-01-01

    a numerical heat and mass transport model that includes full coupling of heat, moisture and ion transport. Heat, moisture, and chloride concentration distributions were passed to a simplified reinforcement corrosion initiation and propagation model. The numerical study indicates that processing and temporal...... resolution of the exposure data has a considerable impact on long-term hygrothermal distribution, chloride ingress, and reinforcement section loss results. Use of time-averaged exposure data in the heat and mass transport model reduces the rate of chloride ingress in concrete and affects prediction...... of reinforcement corrosion initiation and propagation. Randomly sampled exposure data at daily, weekly, or monthly resolution yields prediction of reinforcement corrosion initiation and propagation closer to original resolution results than time-averaged exposure data....

  14. 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.

  15. 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.

  16. Chloride regulates afferent arteriolar contraction in response to depolarization

    DEFF Research Database (Denmark)

    Hansen, P B; Jensen, B L; Skott, O

    1998-01-01

    -Renal vascular reactivity is influenced by the level of dietary salt intake. Recent in vitro data suggest that afferent arteriolar contractility is modulated by extracellular chloride. In the present study, we assessed the influence of chloride on K+-induced contraction in isolated perfused rabbit...... afferent arterioles. In 70% of vessels examined, K+-induced contraction was abolished by acute substitution of bath chloride. Consecutive addition of Cl- (30, 60, 80, 100, 110, and 117 mmol/L) restored the sensitivity to K+, and half-maximal response was observed at 82 mmol/L chloride. The calcium channel...... antagonist diltiazem (10(-6) mol/L) abolished K+-induced contractions. Bicarbonate did not modify the sensitivity to chloride. Norepinephrine (10(-6) mol/L) induced full contraction in depolarized vessels even in the absence of chloride. Iodide and nitrate were substituted for chloride with no inhibitory...

  17. Use of a liquid-phase ion gun for local breakdown of the passive film on iron

    Energy Technology Data Exchange (ETDEWEB)

    Fushimi, Koji; Azumi, Kazuhisa; Seo, Masahiro

    2000-02-01

    A silver/silver chloride microelectrode was developed as a liquid-phase ion gun for investigation of precursor processes of pitting corrosion. This electrode was set as a probe electrode of a scanning electrochemical microscope and used to induce a local breakdown of passive film on iron. A small amount of chloride ions generated by cathodic polarization of the silver/silver chloride microelectrode has succeeded in inducing the local breakdown of the passive film formed on iron in deaerated pH 6.5 borate solution. Moreover, the microelectrode could detect ferric ions dissolved from the film at the initial stage of the film breakdown.

  18. 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...

  19. 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. PMID:18487638

  20. 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.

  1. 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 inhibitors (thiocyanate, furosemide, phloretin, and acetazolamide) also affects chloride exchange diffusion, hyperpolarization current as well as chloride influx during hyperpolarization. Although in some cases, effects on the short circuit current were also observed none of the effects on chloride transport....... On the basis of these findings, and the results reported in the previous paper (Hviid Larsen and Kristensen 1977) it is considered probable that the membrane molecules responsible to chloride exchange diffusion under short circuit conditions, are rearranged under the influence of a hyperpolarizing clamping...

  2. 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.

  3. Combinación de sistemas de flujo de baja y alta presion para la determinacion de Mg, Ca y Sr en salmueras por espectrofotometria de absorcion atomica con llama

    Directory of Open Access Journals (Sweden)

    Neira José

    2001-01-01

    Full Text Available This article describes the combination of low- and high-pressure flow systems for the determination of Magnesium, Calcium and Strontium by flame atomic absorption spectrometry (FAAS. In the low-pressure system a short C-18 RP column (length 0,5 cm was utilized for the preconcentration/matrix separation step, xylenol orange was used as chelating agent and tetrabutylamonium acetate for ion pair formation. The hydraulic high pressure nebulization (HHPN was used for sample transport and sample introduction in the high pressure system. The repeatabilities and detection limits for Mg, Ca and Sr were determined and compared with those obtained by pneumatic nebulization (PN. The results show that the detection limits obtained using the HHPN for Mg, Ca and Sr are between 1.5 to 2 times better than those obtained by PN when the signal transient was measured in area. The system presented a sampling frequency of 130 h-1 for direct determination of Mg, Ca or Sr in samples of saturated sodium chloride used in the production of chlorine and sodium hydroxide.

  4. A chloride tolerant laccase from the plant pathogen ascomycete Botrytis aclada expressed at high levels in Pichia pastoris.

    Science.gov (United States)

    Kittl, Roman; Mueangtoom, Kitti; Gonaus, Christoph; Khazaneh, Shima Tahvilda; Sygmund, Christoph; Haltrich, Dietmar; Ludwig, Roland

    2012-01-20

    Fungal laccases from basidiomycetous fungi are thoroughly investigated in respect of catalytic mechanism and industrial applications, but the number of reported and well characterized ascomycetous laccases is much smaller although they exhibit interesting catalytic properties. We report on a highly chloride tolerant laccase produced by the plant pathogen ascomycete Botrytis aclada, which was recombinantly expressed in Pichia pastoris with an extremely high yield and purified to homogeneity. In a fed-batch fermentation, 495 mg L(-1) of laccase was measured in the medium, which is the highest concentration obtained for a laccase by a yeast expression system. The recombinant B. aclada laccase has a typical molecular mass of 61,565 Da for the amino acid chain. The pI is approximately 2.4, a very low value for a laccase. Glycosyl residues attached to the recombinant protein make up for approximately 27% of the total protein mass. B. aclada laccase exhibits very low K(M) values and high substrate turnover numbers for phenolic and non-phenolic substrates at acidic and near neutral pH. The enzyme's stability increases in the presence of chloride ions and, even more important, its substrate turnover is only weakly inhibited by chloride ions (I(50)=1.4M), which is in sharp contrast to most other described laccases. This high chloride tolerance is mandatory for some applications such as implantable biofuel cells and laccase catalyzed reactions, which suffer from the presence of chloride ions. The high expression yield permits fast and easy production for further basic and applied research. PMID:22178779

  5. 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.

  6. A mechanism for solvent extraction of first row transition metals from chloride media with the ionic liquid tetraoctylammonium oleate.

    Science.gov (United States)

    Parmentier, Dries; Vander Hoogerstraete, Tom; Banerjee, Dipanjan; Valia, Yash A; Metz, Sybrand J; Binnemans, Koen; Kroon, Maaike C

    2016-06-21

    Aqueous waste streams of the metallurgical industry often contain considerable concentrations of metal salts. Previous research showed that the metal chloride salts of zinc(ii), manganese(ii) and iron(iii) can be recovered by solvent extraction using a sustainable and renewable fatty acid based ionic liquid as the extractant. In this paper, the extraction mechanism of Zn(ii), Co(ii) and Ni(ii) from chloride media has been studied systematically. The metal extraction performances of the precursors, sodium oleate and tetraoctylammonium chloride, were compared to the extraction performance of the ionic liquid tetraoctylammonium oleate. Slope analysis experiments were performed to determine the number of ionic liquid molecules involved in the extraction. The experimental data showed that Co(ii) and Ni(ii) were extracted in the pH range from 6 to 8 by the formation of negatively charged metal carboxylate complexes with tetraalkylammonium counter ions. In contrast, Zn(ii) gets extracted as a mixed metal chloride carboxylate anionic complex with tetraalkylammonium counter ions. This extraction mechanism was supported by EXAFS measurements.

  7. Sodium and chloride levels in rainfall, mist. streamwater and groundwater at the Plynlimon catchments, mid-Wales: inferences on hydrological and chemical controls

    Science.gov (United States)

    Neal, C.; Kirchner, J. W.

    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 salinity is high. This

  8. Corrosion of alloy 22 in phosphate and chloride containing solutions

    International Nuclear Information System (INIS)

    Alloy C-22 is a Ni-based alloy (22% Cr, 13% Mo, 3% W y 3% Fe in weight per cent) that exhibits an excellent uniform and localized corrosion resistance due to its protective passive film. It was designed to resist the most aggressive environments for industrial applications. Alloy 22 is one of the candidates to be considered for the outer shell of the canister that would contain high level radioactive nuclear wastes. The effect of phosphate ion in chloride containing solutions at 90 C degrees was studied under aggressive conditions were this material might be susceptible to crevice corrosion. The electrolyte solution, which consisted of 1M NaCl and different phosphate concentrations (between 10-3M and 1M), was deoxygenated by bubbling with nitrogen. Electrochemical tests, electron microscope observations (SEM) and energy dispersive spectrometer analysis (EDS) were conducted. Crevice corrosion was not detected and the comparison of the potentiodynamic polarization tests showed an increase of the passivity range in phosphate containing solutions. The passive current value was 1 μA/cm2 approximately in all the tests that were performed in this work. The differences in composition of the anodic film formed on the samples suggest that phosphate is responsible for the increase of the passivity range by incorporation to the passive film. (author)

  9. 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.

  10. Experimental evidence for the participation of deep eutectic solvents in silver chloride crystal formation at low temperature

    Science.gov (United States)

    Bhatt, Jitkumar; Mondal, Dibyendu; Prasad, Kamalesh

    2016-05-01

    Deep eutectic solvents (DESs) obtained by the complexation of choline chloride (ChoCl) as hydrogen bond acceptor and hydrogen bond donors such as ethylene glycol (ChoCl-EG 1:2) and glycerol (ChoCl-Gly 1:2) were used as media for the formation of AgCl crystals. Although formation of AgCl crystals was observed in both the solvents but the rate of formation of crystals was faster in ChoCl-EG 1:2 at low temperature (4-5 °C). In the crystals, cholinium cations were found to be present with chloride ions bridged with Ag ions resulting generation of 1D network of AgCl2 anions.

  11. Chloride diffusion in partially saturated cementitious material

    DEFF Research Database (Denmark)

    Nielsen, Erik Pram; Geiker, Mette Rica

    2003-01-01

    The paper proposes a combined application of composite theory and Powers' model for microstructural development for the estimation of the diffusion coefficient as a function of the moisture content of a defect-free cementitious material. Measurements of chloride diffusion in mortar samples (440 kg....../m(3) rapid-hardening Portland cement, w/c = 0.5, maturity minimum 6 months) stored at 65% and 85% RH, as well as in vacuum-saturated mortar samples, illustrate the applicability of the method. (C) 2003 Elsevier Science Ltd. All rights reserved....

  12. Oral cadmium chloride intoxication in mice

    DEFF Research Database (Denmark)

    Andersen, O; Nielsen, J B; Svendsen, P

    1988-01-01

    Diethyldithiocarbamate (DDC) is known to alleviate acute toxicity due to injection of cadmium salts. However, when cadmium chloride was administered by the oral route, DDC enhanced rather than alleviated the acute toxicity; both oral and intraperitoneal (i.p.) administration of DDC had this effect....... Thus, orally administered DDC enhanced cadmium-induced duodenal and ileal tissue damage and inhibition of peristalsis, as indicated by an increased intestinal transit time. At low cadmium doses, the whole-body retention of cadmium was increased by oral DDC administration. Intraperitoneally administered...

  13. N-(2-Benzoylethylpropan-2-aminium chloride

    Directory of Open Access Journals (Sweden)

    Abdullah Aydın

    2012-09-01

    Full Text Available In the title salt, C12H18NO+·Cl−, N—H...Cl interactions between the free chloride anions and the organic cations connect the molecules into hydrogen-bond dimers, forming a R22(8 motif. The dimers are linked by C—H...O hydrogen bonds into chains extending along [301]. The carbonyl group is co-planar with the phenyl ring [C—C—C=O torsion angle = −3.3 (7°]. The side chain has an E conformation.

  14. Effect of chloride concentration and pH on pitting corrosion of waste package container materials

    International Nuclear Information System (INIS)

    Electrochemical cyclic potentiodynamic polarization experiments were performed on several candidate waste package container materials to evaluate their susceptibility to pitting corrosion at 90 degrees C in aqueous environments relevant to the potential underground high-level nuclear waste repository. Results indicate that of all the materials tested, Alloy C-22 and Ti Grade-12 exhibited the maximum corrosion resistance, showing no pitting or observable corrosion in any environment tested. Efforts were also made to study the effect of chloride ion concentration and pH on the measured corrosion potential (Ecorr), critical pitting and protection potential values

  15. 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...

  16. 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

  17. Resistivity features in intercalated graphite compounds with bromine and iodine chloride in the region of structural phase transitions in the layer of intercalate

    International Nuclear Information System (INIS)

    In the paper anomalous changes of resistivity in graphite intercalated compounds with iodine chloride and bromine are investigated in the phase transition temperature interval. It is shown that these anomalies are caused by the change of carriers mobility in the phase transitional interval as well as by the origin of ''mobile ions liquids''

  18. 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.

  19. 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.

  20. Interactions between chloride ingress and carbonation in cementitious materials

    OpenAIRE

    SAILLIO, Mickael; BARBERON, Fabien; BAROGHEL BOUNY, Véronique; GEGOUT, Philippe; PLATRET, Gérard; D'ESPINOSE DE LA CAILLERIE, JB

    2011-01-01

    Carbonation and chloride attacks are the major causes of reinforced concrete (RC) structure deterioration by initiation of steel rebar corrosion. These attacks are usually studied separately in the literature. Chloride-induced corrosion takes place mainly in marine environment or in the case of contact with deicing salts, while carbonation is systematically present in all RC structures at a variable degree. Since carbonation leads to significant microstructure changes, the effect of chloride ...

  1. Open cycle lithium chloride cooling system

    Science.gov (United States)

    Lenz, T. G.; Loef, G. O. G.; Iyer, R.; Wenger, J.

    1983-05-01

    A lithium chloride open cycle absorption chiller has been designed, built and tested. Solution reconcentration takes place in a small counter current packed column supplied with solar heated air. Removal of noncondensable gases that enter the chiller dissolved in the strong solution and the make-up refrigerant streams is accomplished by a liquid-jet ejector and a small vacuum pump. Cooling capacities approaching 1.4 tons and COP levels of 0.58 have been achieved at non-optimum operating conditions. Test results from preliminary system operation suggest that mass transfer processes in both the packed column reconcentrator and the absorber are controlled by concentration gradients in the lithium chloride solution. Liquid phase controlled mass transfer dictates an operating strategy different from the previously assumed gas phase controlled process to obtain maximum rates of evaporation in the packed column. Determination of optimal operating conditions leading to decreased electrical power consumption and improved cooling capacity and coefficient of performance will require further analysis and testing.

  2. Synthesis and structure characterization of diethyldiallylammonium chloride

    Institute of Scientific and Technical Information of China (English)

    刘立华; 龚竹青; 郑雅杰

    2003-01-01

    The unsaturated quaternary ammonium salt diethyldiallylammonium chloride(DEDAAC) was synthesized in a two-step synthetic method. The influences of the adding method of raw materials and temperature on the yields of diethylallylamine (DEAA), and drying and temperature on the synthesis of DEDAAC were investigated. The content of in-process product DEAA was determined by non-aqueous titration. The structure of product DEDAAC was identified with IR, 1 H NMR and elemental analysis. The results show that adding allyl chloride and sodium hydroxide alternately can increase the yield of DEAA and decrease by-products. In further synthesizing of DEDAAC from DEAA, the step of drying DEAA is very necessary. When DEAA is dried by solid sodium hydroxide, good columnar crystals with a high purity(mp 199.5-201.0 ℃) are obtained; when DEAA is undried or the content of water in DEAA is above 20%, only platelets with bad quality are obtained even without crystals. The suitable synthesis conditions for DEAA and DEDAAC are 35 ℃, 6 h and 40 ℃, 36 h, respectively, and their yields are 69.7% and 67.3%, respectively.

  3. Fault locator of an allyl chloride plant

    Directory of Open Access Journals (Sweden)

    Savković-Stevanović Jelenka B.

    2004-01-01

    Full Text Available Process safety analysis, which includes qualitative fault event identification, the relative frequency and event probability functions, as well as consequence analysis, was performed on an allye chloride plant. An event tree for fault diagnosis and cognitive reliability analysis, as well as a troubleshooting system, were developed. Fuzzy inductive reasoning illustrated the advantages compared to crisp inductive reasoning. A qualitative model forecast the future behavior of the system in the case of accident detection and then compared it with the actual measured data. A cognitive model including qualitative and quantitative information by fuzzy logic of the incident scenario was derived as a fault locator for an ally! chloride plant. The obtained results showed the successful application of cognitive dispersion modeling to process safety analysis. A fuzzy inductive reasoner illustrated good performance to discriminate between different types of malfunctions. This fault locator allowed risk analysis and the construction of a fault tolerant system. This study is the first report in the literature showing the cognitive reliability analysis method.

  4. Microscale adaptation of the potentiometric method with ion-selective electrode for the quantification of fluoride; Adaptacion a microescala del metodo potenciometrico con electrodo ion selectivo para la cuantificacion de fluoruro

    Energy Technology Data Exchange (ETDEWEB)

    Guevara Ruiz, Paulina; Ortiz Perez, Maria Deogracias [Laboratorio de Bioquimica, Facultad de de Medicina, Universidad Autonoma de San Luis Potosi, San Luis Potosi, San Luis Potosi, (Mexico)]. E-mail: mdortiz@uaslp.mx

    2009-05-15

    Similarly to other countries, ground water from Mexico is naturally polluted by fluoride. The main effects of fluoride at typical ground water concentrations are dental fluorosis, neurological deficits and reproductive disorders. In order to verify that the fluoride concentration is within the allowed guideline in Mexico (NOM 127 and 201), it is important to monitor fluoride levels in water and commercial beverages. The aim of this work is to develop a modification of the standard potentiometric method for fluoride determination in water, in order to reduce costs and amount of potentially toxic waste substances. Both methods were validated, the standard potentiometric method with the ion selective electrode and the microscale modification proposed in this paper. The methods were compared using statistic tests and graphics, followed by the comparison of 125 samples of commercial bottled water sold in the city of San Luis Potosi. Optimal results were obtained for the validation of both methods, and the microscale modification showed statistically identical results to those obtained with the standard method in all samples of bottled water. The microscale modification is a good alternative for fluoride assessment in water and beverages, and it represents a 95 % reduction of costs and chemical waste. [Spanish] En varios paises, incluido Mexico se presenta una contaminacion natural con fluoruro en agua subterranea; los principales efectos en la salud observados en poblacion expuesta a concentraciones mayores al valor permisible (que en Mexico es de 1.5 mg/L) son la fluorosis dental y esqueletica, asi como dano reproductivo y neurologico. En varios estados de la republica Mexicana, este problema es aun desconocido, de ahi la necesidad de evaluar las concentraciones de fluoruro en agua de consumo en varias comunidades. Asi, el objetivo de este trabajo es desarrollar un metodo a microescala para la determinacion de fluoruro en agua, que al reducir la cantidad de reactivo y

  5. 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.

  6. On Barium Oxide Solubility in Barium-Containing Chloride Melts

    Science.gov (United States)

    Nikolaeva, Elena V.; Zakiryanova, Irina D.; Bovet, Andrey L.; Korzun, Iraida V.

    2016-08-01

    Oxide solubility in chloride melts depends on temperature and composition of molten solvent. The solubility of barium oxide in the solvents with barium chloride content is essentially higher than that in molten alkali chlorides. Spectral data demonstrate the existence of oxychloride ionic groupings in such melts. This work presents the results of the BaO solubility in two molten BaCl2-NaCl systems with different barium chloride content. The received data together with earlier published results revealed the main regularities of BaO solubility in molten BaO-BaCl2-MCl systems.

  7. Durability of cracked fibre reinforced concrete structures exposed to chlorides

    DEFF Research Database (Denmark)

    Hansen, Ernst Jan De Place; Ekman, Tom; Hansen, Kurt Kielsgaard

    1999-01-01

    is used as environmental load. The chloride penetration is characterized both qualitatively (UV-test) and quantitatively (chloride profile) and by microscopy. The test programme involves three different concrete qualities. Both steel fibres and polypropylene fibres are used in the concrete beams as well......Durability studies are carried out by subjecting FRC-beams to combined mechanical and environmental load. Mechanical load is obtained by exposing beams to 4-point bending until a predefined crack width is reached, using a newly developed test setup. Exposure to a concentrated chloride solution...... as main reinforcement. The effect of the cracks, the fibres and the concrete quality on the chloride penetration is studied....

  8. Physiology and Pathophysiology of CLC-1: Mechanisms of a Chloride Channel Disease, Myotonia

    Directory of Open Access Journals (Sweden)

    Chih-Yung Tang

    2011-01-01

    Full Text Available The CLC-1 chloride channel, a member of the CLC-channel/transporter family, plays important roles for the physiological functions of skeletal muscles. The opening of this chloride channel is voltage dependent and is also regulated by protons and chloride ions. Mutations of the gene encoding CLC-1 result in a genetic disease, myotonia congenita, which can be inherited as an autosmal dominant (Thomsen type or an autosomal recessive (Becker type pattern. These mutations are scattered throughout the entire protein sequence, and no clear relationship exists between the inheritance pattern of the mutation and the location of the mutation in the channel protein. The inheritance pattern of some but not all myotonia mutants can be explained by a working hypothesis that these mutations may exert a “dominant negative” effect on the gating function of the channel. However, other mutations may be due to different pathophysiological mechanisms, such as the defect of protein trafficking to membranes. Thus, the underlying mechanisms of myotonia are likely to be quite diverse, and elucidating the pathophysiology of myotonia mutations will require the understanding of multiple molecular/cellular mechanisms of CLC-1 channels in skeletal muscles, including molecular operation, protein synthesis, and membrane trafficking mechanisms.

  9. Experimental Investigation on Pore Structure Characterization of Concrete Exposed to Water and Chlorides

    Directory of Open Access Journals (Sweden)

    Jun Liu

    2014-09-01

    Full Text Available 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 more evident than the cement hydration effect. From the experimental data, Ca(OH2 is leached considerably with the increase in immersion time. The pore structure of concrete can also be affected by the formation of an oriented structure of water in concrete materials; (ii incorporation of fly ash makes a difference for the performance of concrete submersed in solutions as the total porosity and the pore connectivity can be lower. Especially when the dosage of fly ash is up to 30%, the pores with the diameter of larger than 100 nm show significant decrease. It demonstrates that the pore properties are improved by fly ash, which enhances the resistance against the calcium leaching; (iii chlorides have a significant impact on microstructure of concrete materials because of the chemical interactions between the chlorides and cement hydrates.

  10. Photothermal Conversion of F-centres in Additively Coloured Potassium Chloride Crystals with Cationic and Anionic Impurities

    Directory of Open Access Journals (Sweden)

    Vladimirov D.A.

    2004-12-01

    Full Text Available The compensating influence of cationic (Ca++ ions and anionic (OH– ions impurities doped into additively coloured potassium chloride crystal on the process of photothermal conversion of F-centres is detected. “Brightening” in the absorption band of the F-centres is revealed that achieves 90%. It is not accompanied by the appearance of centres absorbing in the visible range. Double vacancies and the complexes Ca++(OH–2-cationic vacancy are shown to be responsible for this phenomenon. Basing on those results, a new system for holographic recording is suggested that uses the compensating effect of cationic and anionic impurities .

  11. Sorption recovery of platinum (II, IV in presence of copper (II and zinc (II from chloride solutions

    Directory of Open Access Journals (Sweden)

    Kononova Olga N.

    2015-01-01

    Full Text Available The sorption preconcentration of platinum (II, IV ions was investigated in presence of accompanying copper (II and zinc (II ions from chloride solutions on the new ion exchangers CYBBER (Russia, previously unexplored. The initial concentrations of platinum and accompanying ions were 0.25 mmol L-1 and 2.0 mmol L-1, respectively, and the acidity of medium was 0.001 - 4.0 mol L-1. It was shown that the resins investigated - strong and weak basic anion exchangers as well as chelate ion exchangers - possess good sorption and kinetic properties. The simultaneous sorption of investigated ions results in the complete recovery of platinum, while the non-ferrous metal ions are sorbed at less than 20%. Followed by the selective elution of platinum by thiourea (80 g L-1 solution in 0.3 M H2SO4, the quantitative isolation of platinum was achieved (more than 90%. Therefore, the studied ion exchangers can be recommended for recovery and separation of Pt(II,IV, Cu(II and Zn(II ions.

  12. 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.

  13. Effect of pH and chloride concentration on the removal of hexavalent chromium in a batch electrocoagulation reactor

    Energy Technology Data Exchange (ETDEWEB)

    Arroyo, M.G. [Departamento de Ingenieria Quimica y Nuclear, Universidad Politecnica de Valencia, Camino de Vera s/n, 46022 Valencia (Spain); Perez-Herranz, V., E-mail: vperez@iqn.upv.es [Departamento de Ingenieria Quimica y Nuclear, Universidad Politecnica de Valencia, Camino de Vera s/n, 46022 Valencia (Spain); Montanes, M.T.; Garcia-Anton, J.; Guinon, J.L. [Departamento de Ingenieria Quimica y Nuclear, Universidad Politecnica de Valencia, Camino de Vera s/n, 46022 Valencia (Spain)

    2009-09-30

    In this work, the effect of pH and chloride ions concentration on the removal of Cr(VI) from wastewater by batch electrocoagulation using iron plate electrodes has been investigated. The initial solution pH was adjusted with different concentrations of H{sub 2}SO{sub 4}. The presence of chloride ions enhances the anode dissolution due to pitting corrosion. Fe{sup 2+} ions formed during the anode dissolution cause the reduction of Cr(VI) to form Cr(III), which are co-precipitated with Fe{sup 3+} ions at relatively low pH. The reduction degree of Cr(VI) to Cr(III) and the solubility of metal hydroxide species (both chromic and iron hydroxides) depend on pH. At higher concentrations of H{sub 2}SO{sub 4}, the reduction of Cr(VI) to Cr(III) by Fe{sup 2+} ions is preferred, but the coagulation of Fe{sup 3+} and Cr(III) is favoured at the lower H{sub 2}SO{sub 4} concentrations.

  14. 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.

  15. THE COMPATIBILITY OF BLENDS OF POLY(VINYL CHLORIDE) OR CHLORINATED POLY(VINYL CHLORIDE) WITH POLY(METHYL METHACRYLATE)

    Institute of Scientific and Technical Information of China (English)

    WANG Qingguo; CHENG Rongshi

    1988-01-01

    IR spectral shifts of carbonyl vibrational absorption for ethyl acetate, which acts analogically as the structural unit of poly(methyl methacrylate), in cyclohexane, chloroform, chlorinated paraffins, poly(vinyl chloride) and chlorinated poly(vinyl chloride) were measured. The results suggest that there are specific interactions between the carbonyl groups and the chlorinated hydrocarbons which could be responsible for the apparent compatibility of poly(vinyl chloride) -poly(methyl methacrylate) and chlorinated poly(vinyl chloride) -poly(methyl methacrylate) blends. Additionally, the effects of the preparation mode of blend films on phase separation and observed compatibility are discussed.

  16. Surface modification of poly (vinyl chloride) by long-distance and direct argon RF plasma

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    This paper reports the effects of long- distance and direct argon radio frequency (RF) plasma surface treatment on polyvinyl chloride (PVC) films in terms of changes in surface wettability and surface chemistry. The surface properties are characterized by the water contact angle measurement, X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The mechanism is further analyzed and the role of all kinds of active species, e.g. electrons, ions and free radicals involved in plasma surface modification is further evaluated. Results show that the long-distance and direct RF plasma treatments modify the PVC surface in morphology and composition, and both modifications cause surface oxidation of PVC films, in the forming of functional groups enhancing polymer wettability. The effect of the long-distance argon RF plasma is more notable. This suggests that long-distance argon RF plasma could restrain the ion and electron eroding effect and enhance free radical reaction.

  17. Effect of sodium chloride on photosynthetic 14CO2 assimilation in Portulaca oleracea Linn

    International Nuclear Information System (INIS)

    Effect of NaCl on ion uptake, photosynthetic rate and photosynthetic products in a C4 non-CAM succulent, P. oleracea has been investigated. NaCl causes accumulation of Na as well as Cl ions with decrease in K and Ca contents. Chlorophylls and photosynthetic 14CO2 fixation rates are adversely affected due to sodium chloride salinity. Plants grown in the presence of NaCl show increase in C4 acid percentage with increase in labelling of organic acids in light. Labelling of amino acids (particularly alanine) and sugars (sucrose) is affected by NaCl. Enzyme studies reveal that PEP-carboxylase is stimulated at all concentrations of NaCl but higher concentrations affected the activity of RuBP-Carboxylase. (author)

  18. Extraction studies of cobalt (Ⅱ) and nickel (Ⅱ) from chloride solution using PC88A

    Institute of Scientific and Technical Information of China (English)

    LUO Lin; WEI Jian-hong; WU Gen-yi; F. TOYOHISA; S. ATSUSHI

    2006-01-01

    Solvent extraction study of cobalt and nickel were carried out from a chloride solution with a high ratio of Co to Ni using the sodium salt of PC88A as extractant diluted in kerosene. The solution was generated in batches by leaching a tungsten super alloy scraps. The results show that extraction rate of metal ions increases with increase of aqueous phase pH value. The pH0.5 value difference of 1.40 with PC88A indicates the possible separation of cobalt and nickel. Increase of the concentration of the solvent can enhance the percentage extraction of both metal ions. Improvement of temperature is beneficial to extraction separation of cobalt and nickel. Extraction and stripping processes were also studied in a cross-current solvent extraction unit and the results were also given.

  19. Preparation of anion exchange membrane using polyvinyl chloride (PVC) for alkaline water electrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Gab-Jin; Bong, Soo-Yeon; Ryu, Cheol-Hwi [Hoseo University, Asan (Korea, Republic of); Lim, Soo-Gon [Energy and Machinery Korea Co., Ltd., Changwon (Korea, Republic of); Choi, Ho-Sang [Kyungil University, Gyeongsan (Korea, Republic of)

    2015-09-15

    An anion exchange membrane was prepared by the chloromethylation and the amination of polyvinyl chloride (PVC), as the base polymer. The membrane properties of the prepared anion exchange membrane, including ionic conductivity, ion exchange capacity, and water content were measured. The ionic conductivity of the prepared anion exchange membrane was in the range of 0.098x10{sup -2} -7.0x10{sup -2}S cm{sup -1}. The ranges of ion exchange capacity and water content were 1.9-3.7meq./g-dry-membrane and 35.1-63.1%, respectively. The chemical stability of the prepared anion exchange membrane was tested by soaking in 30 wt% KOH solution to determine its availability as a separator in the alkaline water electrolysis. The ionic conductivity during the chemical stability test largely did not change.

  20. Ion colliders

    International Nuclear Information System (INIS)

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