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Sample records for alkaline salt solution

  1. Solubility of pllutonium in alkaline salt solutions

    International Nuclear Information System (INIS)

    Plutonium solubility data from several studies have been evaluated. For each data set, a predictive model has been developed where appropriate. In addition, a statistical model and corresponding prediction intervals for plutonium solubility as a quadratic function of the hydroxide concentration have been developed. Because of the wide range of solution compositions, the solubility of plutonium can vary by as much as three orders of magnitude for any given hydroxide concentration and still remain within the prediction interval. Any nuclear safety assessments that depend on the maximum amount of plutonium dissolved in alkaline salt solutions should use concentrations at least as great as the upper prediction limits developed in this study. To increase the confidence in the prediction model, it is recommended that additional solubility tests be conducted at low hydroxide concentrations and with all of the other solution components involved. To validate the model for application to actual waste solutions, it is recommended that the plutonium solubilities in actual waste solutions be determined and compared to the values predicted by the quadratic model

  2. Characterization of Laboratory Prepared Concrete Pastes Exposed to High Alkaline and High Sodium Salt Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Langton, C. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-06-30

    The objective of this study was to identify potential chemical degradation mechanisms for the Saltstone Disposal Unit (SDU) concretes, which over the performance life of the structures may be exposed to highly alkaline sodium salt solutions containing sulfate, hydroxide, and other potentially corrosive chemicals in salt solution and saltstone flush water, drain water, leachate and / or pore solution. The samples analyzed in this study were cement pastes prepared in the SIMCO Technologies, Inc. concrete laboratory. They were based on the paste fractions of the concretes used to construct the Saltstone Disposal Units (SDUs). SDU 1 and 4 concrete pastes were represented by the PV1 test specimens. The paste in the SDU 2, 3, 5, and 6 concrete was represented by the PV2 test specimens. SIMCO Technologies, Inc. selected the chemicals and proportions in the aggressive solutions to approximate proportions in the saltstone pore solution [2, 3, 5, and 6]. These test specimens were cured for 56 days in curing chamber before being immersed in aggressive solutions. After exposure, the samples were frozen to prevent additional chemical transport and reaction. Selected archived (retrieved from the freezer) samples were sent to the Savannah River National Laboratory (SRNL) for additional characterization using x-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive x-ray (EDX) spectroscopy. Characterization results are summarized in this report. In addition, a correlation between the oxide composition of the pastes and their chemical durability in the alkaline salt solutions is provided.

  3. Technetium recovery from high alkaline solution

    Science.gov (United States)

    Nash, Charles A.

    2016-07-12

    Disclosed are methods for recovering technetium from a highly alkaline solution. The highly alkaline solution can be a liquid waste solution from a nuclear waste processing system. Methods can include combining the solution with a reductant capable of reducing technetium at the high pH of the solution and adding to or forming in the solution an adsorbent capable of adsorbing the precipitated technetium at the high pH of the solution.

  4. Physiological and Molecular Features of Puccinellia tenuiflora Tolerating Salt and Alkaline-Salt Stress

    Institute of Scientific and Technical Information of China (English)

    Xia Zhang; Liqin Wei; Zizhang Wang; Tai Wang

    2013-01-01

    Saline-alkali soil seriously threatens agriculture productivity; therefore,understanding the mechanism of plant tolerance to alkaline-salt stress has become a major challenge.Halophytic Puccinellia tenuiflora can tolerate salt and alkaline-salt stress,and is thus an ideal plant for studying this tolerance mechanism.In this study,we examined the salt and alkaline-salt stress tolerance of P.tenuiflora,and analyzed gene expression profiles under these stresses.Physiological experiments revealed that P.tenuiflora can grow normally with maximum stress under 600 mmol/L NaCl and 150 mmol/L Na2CO3 (pH 11.0)for 6 d.We identified 4,982 unigenes closely homologous to rice and barley.Furthermore,1,105 genes showed differentially expressed profiles under salt and alkaline-salt treatments.Differentially expressed genes were overrepresented in functions of photosynthesis,oxidation reduction,signal transduction,and transcription regulation.Almost all genes downregulated under salt and alkaline-salt stress were related to cell structure,photosynthesis,and protein synthesis.Comparing with salt stress,alkaline-salt stress triggered more differentially expressed genes and significantly upregulated genes related to H+ transport and citric acid synthesis.These data indicate common and diverse features of salt and alkalinesalt stress tolerance,and give novel insights into the molecular and physiological mechanisms of plant salt and alkaline-salt tolerance.

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

    International Nuclear Information System (INIS)

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

  6. Electrochemical processing of alkaline nitrate and nitrite solutions

    International Nuclear Information System (INIS)

    Processing of high-level waste at the Savannah River Plant (SRP) will produce, as a by product, a low- level, alkaline salt solution containing approximately 17% sodium nitrate and sodium nitrite. This solution will be incorporated into a cement formulation, saltstone, and placed in an engineered landfill. Electrochemical methods have been investigated to decrease the nitrate and nitrite in this solution in order to lower the leaching of nitrate and nitrite from saltstone and to reduce the volume of saltstone. Laboratory experiments have demonstrated the technical feasibility of electrolytically reducing the nitrate and nitrite in a synthetic salt solution similar in composition to that expected to be produced at SRP. Greater than 99% of the sodium nitrate and sodium nitrite can be reduced, producing ammonia, nitrogen, oxygen, and sodium hydroxide. In addition, significant reductions in the volume of saltstone may be realized if the sodium hydroxide produced by electrolysis can be recycled

  7. Electrolytic denitrification of alkaline nitrate and nitrite solution

    International Nuclear Information System (INIS)

    Processing of high-level waste at the Savannah River Plant (SRP) will produce a low-level alkaline salt solution, containing approximately 17% sodium nitrate and sodium nitrite. This solution will be incorporated into a cement wasteform, saltstone, and placed in an engineered landfill. Laboratory experiments have demonstrated the technical feasibility of electrochemically reducing the nitrate and nitrite in a synthetic, nonradioactive salt solution similar in composition to that expected to be produced at SRP. Greater than ninety-five percent of the sodium nitrate and sodium nitrite can be reduced electrolytically, producing ammonia, nitrogen, oxygen, and sodium hydroxide. Reduction of the nitrate and nitrite will reduce the leaching of nitrate and nitrite from the saltstone monolith. In addition, significant reductions in the volume of saltstone may be realized if the sodium hydroxide produced by electrolysis can be recycled

  8. 40 CFR 721.4668 - Hydrated alkaline earth metal salts of metalloid oxyanions.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Hydrated alkaline earth metal salts of... Specific Chemical Substances § 721.4668 Hydrated alkaline earth metal salts of metalloid oxyanions. (a... hydrated alkaline earth metal salts of metalloid oxyanions (PMN P-94-1557) is subject to reporting...

  9. Alkaline earth cation extraction from acid solution

    Science.gov (United States)

    Dietz, Mark; Horwitz, E. Philip

    2003-01-01

    An extractant medium for extracting alkaline earth cations from an aqueous acidic sample solution is described as are a method and apparatus for using the same. The separation medium is free of diluent, free-flowing and particulate, and comprises a Crown ether that is a 4,4'(5')[C.sub.4 -C.sub.8 -alkylcyclohexano]18-Crown-6 dispersed on an inert substrate material.

  10. Identification of Listeria monocytogenes Genes Involved in Salt and Alkaline-pH Tolerance

    OpenAIRE

    Gardan, Rozenn; Cossart, Pascale; Labadie, Jean

    2003-01-01

    The capacity of Listeria monocytogenes to tolerate salt and alkaline stresses is of particular importance, as this pathogen is often exposed to such environments during food processing and food preservation. We screened a library of Tn917-lacZ insertional mutants in order to identify genes involved in salt and/or alkaline tolerance. We isolated six mutants sensitive to salt stress and 12 mutants sensitive to salt and alkaline stresses. The position of the insertion of the transposon was locat...

  11. Progress of research on the influence of alkaline cation and alkaline solution on bentonite properties

    International Nuclear Information System (INIS)

    Based on the previous laboratory studies and numerical simulation on bentonite in alkaline environments, the effects of alkaline cation and alkaline solution on mineral composition, microstructure, swelling capacity and hydraulic properties of bentonite are emphasized in this paper, temperature, pH values and concentration are discussed as main affecting factors. When bentonite is exposed to alkaline cation or alkaline solution, microstructure of bentonite will be changed due to the dissolution of montmorillonite and the formation of secondary minerals, which results in the decrease of swelling pressure. The amount of the reduction of swelling pressure depends on the concentration of alkaline solution. Temperature, polyvalent cation, salinity and concentration are the main factors affecting hydraulic properties of bentonite under alkaline conditions. Therefore, future research should focus on the mechanism of coupling effects of weak alkaline solutions on the mineral composition, microstructure, swelling capacity and hydraulic properties of bentonite under different temperatures and different pH values. (authors)

  12. Distribution of alkaline earth elements between aqueous solutions and polymer sorbents impregnated by 8-hydroxyquinoline

    International Nuclear Information System (INIS)

    Interphase distribution of alkaline-earth element (AEE) microimpurities between solutions of alkali metal chlorides and macroporous copolymer of styrene with divinylbenzene impregnated by 8-hydroxyquinoline is investigated. The effect of phase composition on AEE and 8-hydroxyquinoline distribution coefficient is considered. Advantages of the mixture sorption with impregnated sorbent as compared with liquid extraction for thorough purification of salt solution are shown

  13. Eco-physiological Characteristics of Alfalfa Seedlings in Response to Various Mixed Salt-alkaline Stresses

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Soil salinization and alkalization frequently co-occur in nature, but little is known about the mixed effects of salt-alkaline stresses on plants. An experiment with mixed salts (NaCl, Na2SO4, NaHCO3 and Na2CO3) and 30 salt-alkaline combinations(salinity 24-120 mmol/L and pH 7.03-10.32) treating Medicago sativa seedlings was conducted. The results demonstrated that salinity and alkalinity significantly affected total biomass and biomass components of seedlings. There were interactive effects of salt composition and concentration on biomass (P ≤ 0.001). The interactions between salinity and alkalinity stresses led to changes in the root activity along the salinity gradient (P ≤ 0.001). The effects of alkalinity on seedling survival rate were more significant than those of salinity, and the seedlings demonstrated some physiological responses(leaf electrolyte leakage rate and proline content) in order to adapt to mixed salt-alkaline stresses. It was concluded that the mixed salt-alkaline stresses, which differ from either salt or alkali stress, emphasize the significant interaction between salt concentration (salinity) and salt component (alkalinity). Further, the effects of the interaction between high alkalinity and salinity are more severe than those of either salt or alkali stress, and such a cooperative interaction results in more sensitive responses of ecological and physiological characteristics in plants.

  14. Process for the separation of uranium in an alkaline solution, particularly extracted from an uraniferous ore

    International Nuclear Information System (INIS)

    Process for the treatment of an alkaline uraniferous liquor containing solubilised uranium, particularly sodium uranyl-tricarbonate, characterised in that this liquor is placed into contact with a cationic ion exchange resin, previously put into ammonium form and, in that after the ion exchange has taken place a solution is collected in which the previous sodium salts and complexes have been mainly transformed in ammonium salts and complexes

  15. Revisiting zinc passivation in alkaline solutions

    International Nuclear Information System (INIS)

    Highlights: • Zinc passive films were characterised by electrochemical tests coupled with cross sectional FIB-SEM. • Passive layers at pH > 12 comprised of an outer precipitated layer and inner compact oxide. • The electrolyte pH influences the nature/stability of the outer precipitated layer and this impacts the passive state on zinc. • The precipitated layers on zinc at pH 12 support cathode reactions and catalyse oxide growth. -- Abstract: Passive films nominally consist of an inner compact oxide and the outer precipitated layer. In the case of zinc (Zn), the outer layer is mainly precipitated ZnO/Zn(OH)2. Electrolyte pH controls the stability of the outer precipitated layer. In a pH 13 solution, formation of soluble Zn(OH)3− and Zn(OH)42− phases render the precipitated layer unstable increasing zinc corrosion, whereas at pH 12, the precipitated layer (ZnO/Zn(OH)2) is more stable making it an effective anodic barrier upon zinc. These precipitated oxides formed at pH 12 support cathodic reactions on their surface which in turn catalyse further oxide growth by a cathodically driven process. Focused ion beam-scanning electron microscopy (FIB-SEM) was used to support some of the electrochemical assertions, revealing the form and morphology of the passive layers that grow upon zinc exposed to alkaline solutions

  16. Distribution of alkaline earth elements between aqueous solutions and polymeric sorbent impregnated with 8-hydroxyquinoline

    International Nuclear Information System (INIS)

    The interphase distribution of microimpurities of alkaline earth elements (AEE) between solutions of alkali metal chlorides and a macroporous styrene-divinyl-benzene copolymer impregnated with 8-hydroxyquinoline was studied. The influence of the phase composition on the distribution coefficients of AEE and 8-hydroxyquinoline was examined. The advantages of sorption of the impurities by an impregnated sorbent over liquid extraction for thorough purification of salt solutions were shown

  17. The aluminum chemistry and corrosion in alkaline solutions

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Jinsuo [International Nuclear System Engineering, MS-K 575, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)], E-mail: jszhang@lanl.gov; Klasky, Marc; Letellier, Bruce C. [International Nuclear System Engineering, MS-K 575, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)

    2009-02-15

    Aluminum-alkaline solution systems are very common in engineering applications including nuclear engineering. Consequently, a thorough knowledge of the chemistry of aluminum and susceptibility to corrosion in alkaline solutions is reviewed. The aluminum corrosion mechanism and corrosion rate are examined based on current experimental data. A review of the phase transitions with aging time and change of environment is also performed. Particular attention is given to effect of organic and inorganic ions. As an example, the effect of boron is examined in detail because of the application in nuclear reactor power systems. Methods on how to reduce the corrosion rate of aluminum in alkaline solutions are also highlighted.

  18. Salting-out and Salting-in in Polyelectrolyte Solutions

    Science.gov (United States)

    Zhang, Pengfei; Wu, Jianzhong; Wang, Zhen-Gang

    The phase behavior of polyelectrolyte (PE) solutions is governed by complicated interplay involving the mixing entropy, excluded volume, chain connectivity, and electrostatic interactions. Here we study the phase behavior of PE solutions in both salt-free condition and with added salt using a liquid-state (LS) theory based thermodynamic model. The LS model accounts or the hard-core repulsion by the Canahan-Starling equation of state, correlations due to chain connectivity by the first-order thermodynamic perturbation theory, and electrostatic correlations by the mean-spherical approximation. In comparison to the prediction from the well-known Voorn-Overbeek theory, the LS model predicts loop-type binodal curves in the salt-PE concentration diagram at temperatures slightly above the critical temperature of PE solution in salt-free case, consistent with the experimental study. The phase separated region shrinks with increasing temperature. Three scenarios of salting-out and salting-in phenomenon are predicted with addition of salts based, depending on the PE concentration.

  19. Electromigration in molten salts and application to isotopic separation of alkaline and alkaline-earth elements

    International Nuclear Information System (INIS)

    The separation of the isotopes of the alkaline-earth elements has been studied using counter-current electromigration in molten bromides. The conditions under which the cathode operates as a bromine electrode for the highest possible currents have been examined. For the separation of calcium, it has been necessary to use a stable CaBr2 - (CaBr2 + KBr) 'chain'. In the case of barium and strontium, it was possible to employ the pure bromides. Enrichment factors of the order of 10 for 48Ca and of the order of 1.5 for the rare isotopes of barium and strontium have been obtained. In the case of magnesium the method is slightly more difficult to apply because of material loss due to the relatively high vapour pressure of the salt requiring the use of electrolyte chains, MgBr2 - CeBr3. A study has been made that has led to a larger-scale application of the method. These are essentially the inhibition of reversible operation of the cathode by traces of water, limiting the intensity which can be tolerated; evacuation of the heat produced by the Joule effect, in the absence of which the separation efficiency is reduced by thermal gradients; corrosion of the materials by molten salts at high temperature. Several cells capable of treating a few kilograms of substance have been put into operation; none of these has lasted long enough to produce a satisfactory enrichment. The method is thus limited actually to yields of the order of a few grams. (author)

  20. Ammonia Solubility in High Concentration Salt Solutions

    Energy Technology Data Exchange (ETDEWEB)

    HEDENGREN, D.C.

    2000-02-01

    Solubility data for ammonia in water and various dilute solutions are abundant in the literature. However, there is a noticeable lack of ammonia solubility data for high salt, basic solutions of various mixtures of salts including those found in many of the Hanford Washington underground waste tanks. As a result, models based on solubility data for dilute salt solutions have been used to extrapolate to high salt solutions. These significant extrapolations need to be checked against actual laboratory data. Some indirect vapor measurements have been made. A more direct approach is to determine the ratio of solubility of ammonia in water to its solubility in high salt solutions. In various experiments, pairs of solutions, one of which is water and the other a high salt solution, are allowed to come to equilibrium with a common ammonia vapor pressure. The ratio of concentrations of ammonia in the two solutions is equal to the ratio of the respective ammonia solubilities (Henry's Law constants) at a given temperature. This information can then be used to refine the models that predict vapor space compositions of ammonia. Ammonia at Hanford is of concern because of its toxicity in the environment and its contribution to the flammability of vapor space gas mixtures in waste tanks.

  1. Ammonia Solubility in High Concentration Salt Solutions

    International Nuclear Information System (INIS)

    Solubility data for ammonia in water and various dilute solutions are abundant in the literature. However, there is a noticeable lack of ammonia solubility data for high salt, basic solutions of various mixtures of salts including those found in many of the Hanford Washington underground waste tanks. As a result, models based on solubility data for dilute salt solutions have been used to extrapolate to high salt solutions. These significant extrapolations need to be checked against actual laboratory data. Some indirect vapor measurements have been made. A more direct approach is to determine the ratio of solubility of ammonia in water to its solubility in high salt solutions. In various experiments, pairs of solutions, one of which is water and the other a high salt solution, are allowed to come to equilibrium with a common ammonia vapor pressure. The ratio of concentrations of ammonia in the two solutions is equal to the ratio of the respective ammonia solubilities (Henry's Law constants) at a given temperature. This information can then be used to refine the models that predict vapor space compositions of ammonia. Ammonia at Hanford is of concern because of its toxicity in the environment and its contribution to the flammability of vapor space gas mixtures in waste tanks

  2. Removal of radioruthenium from alkaline intermediate level radioactive waste solution : a laboratory investigation

    International Nuclear Information System (INIS)

    Various methods were investigated in the laboratory for the removal of radioruthenium from alkaline intermediate level radioactive waste solutions of reprocessing plant origin. The methods included batch equilibration with different ion exchangers and sorbents, column testing and chemical precipitation. A column method using zinc-activated carbon mixture and a chemical precipitation method using ferrous salt along with sodium sulphite were found to be promising for plant scale application. (author). 10 refs., 3 figs., 7 tabs

  3. Transient species produced in irradiated alkaline aqueous solutions containing oxygen

    International Nuclear Information System (INIS)

    The spectra and decay kinetics of the optical absorption in the UV region and at 430nm (maximum of the ozonide ion absorption), were investigated in oxygenated neutral, slightly and strongly alkaline aqueous solutions. It is assumed that the initial absorption after the pulse in oxygenated alkaline solutions is due to the ozonide ion O3-, superoxide radical ion O2- and ozone O3. The long-living absorption in these solutions cannot be excluded as to be probably caused by the ozone O3 or some product formed from O2- or an alkaline stabilized form of this radical-ion. The advantage of applying additional non-optical measurements of the system is shown on the example of H2O2 role played in the mechanism. (author)

  4. Electrolytes. From dilute solutions to fused salts

    International Nuclear Information System (INIS)

    Solutions with composition extending continuously from molecular liquids such as water to fused salts are relatively unusual but of considerable interest. Conductance and thermodynamic properties are considered for several examples. New equations for the activities of the respective components represent the data more accurately than previous treatments and delineate the similarities and differences between such systems and nonelectrolyte solutions

  5. Alkaline solution absorption of carbon dioxide method and apparatus

    Science.gov (United States)

    Hobbs, D.T.

    1991-01-01

    Disclosed is a method for measuring the concentration of hydroxides (or pH) in alkaline solutions, using the tendency of hydroxides to adsorb CO{sub 2}. The method comprises passing CO{sub 2} over the surface of an alkaline solution in a remote tank before and after measurements of the CO{sub 2} concentration. Comparison of the measurements yields the adsorption fraction from which the hydroxide concentration can be calculated using a correlation of hydroxide or pH to adsorption fraction. A schematic is given of a process system according to a preferred embodiment of the invention. 2 figs.

  6. Scorpion toxins prefer salt solutions

    Czech Academy of Sciences Publication Activity Database

    Nikouee, A.; Khabiri, Morteza; Cwiklik, Lukasz

    2015-01-01

    Roč. 21, č. 11 (2015), 287/1-287/14. ISSN 1610-2940 R&D Projects: GA ČR GA13-06181S Institutional support: RVO:61388963 ; RVO:61388955 Keywords : ionic solutions * molecular dynamics * nonaqueous media * secondary structure Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 1.736, year: 2014

  7. Investigation of adsorption interaction of cadmium oxide with antimony (3) in alkaline solutions

    International Nuclear Information System (INIS)

    Adsorption processes on cadmium oxide in pure antimonite alkaline (KOH) solutions and in the presence of organic additions (sodium salt of carboxymethylcellulose, straw oil) have been studied. It is shown, that in the systems being studied, the chemosorptional interaction, leading to a sharp change in the adsorbent surface state is observed. It is established that the formation of a surface high-disperse cadmium oxide-antimony com ound on the cadmium oxide results in practically complete suppression of the cadmium oxide hydration process in aqueous solutions

  8. Qualitative aspects of the degradation of mitomycins in alkaline solution.

    Science.gov (United States)

    Beijnen, J H; den Hartigh, J; Underberg, W J

    1985-01-01

    The major degradation product in alkaline solution of mitomycin A, mitomycin C and porfiromycin is the corresponding 7-hydroxymitosane. The isolation and the physico-chemical and analytical properties of these compounds and their derivatized analogues are discussed. Data are presented on the degradation of mitomycin C at extremely high pH values. PMID:16867711

  9. Potentiodynamic characteristics of cadmium and silver in alkaline solutions

    International Nuclear Information System (INIS)

    The potentiodynamic and ellipsometric characteristics of cadmium and silver in alkaline solutions are studied. The phenomenology of both electrodes shows some common features which are interpreted in termo of a complex hydrated oxide anodic film structure resulting from simultaneous electrochemical and chemical reactions. The kinetics of film growth fits the predictions of nucleation and growth models. (C.L.B.)

  10. Scorpion toxins prefer salt solutions.

    Science.gov (United States)

    Nikouee, Azadeh; Khabiri, Morteza; Cwiklik, Lukasz

    2015-11-01

    There is a wide variety of ion channel types with various types of blockers, making research in this field very complicated. To reduce this complexity, it is essential to study ion channels and their blockers independently. Scorpion toxins, a major class of blockers, are charged short peptides with high affinities for potassium channels. Their high selectivity and inhibitory properties make them an important pharmacological tool for treating autoimmune or nervous system disorders. Scorpion toxins typically have highly charged surfaces and-like other proteins-an intrinsic ability to bind ions (Friedman J Phys Chem B 115(29):9213-9223, 1996; Baldwin Biophys J 71(4):2056-2063, 1996; Vrbka et al. Proc Natl Acad Sci USA 103(42):15440-15444, 2006a; Vrbka et al. J Phys Chem B 110(13):7036-43, 2006b). Thus, their effects on potassium channels are usually investigated in various ionic solutions. In this work, computer simulations of protein structures were performed to analyze the structural properties of the key residues (i.e., those that are presumably involved in contact with the surfaces of the ion channels) of 12 scorpion toxins. The presence of the two most physiologically abundant cations, Na(+) and K(+), was considered. The results indicated that the ion-binding properties of the toxin residues vary. Overall, all of the investigated toxins had more stable structures in ionic solutions than in water. We found that both the number and length of elements in the secondary structure varied depending on the ionic solution used (i.e., in the presence of NaCl or KCl). This study revealed that the ionic solution should be chosen carefully before performing experiments on these toxins. Similarly, the influence of these ions should be taken into consideration in the design of toxin-based pharmaceuticals. PMID:26475740

  11. Americium separations from high salt solutions

    International Nuclear Information System (INIS)

    Americium (III) exhibits an unexpectedly high affinity for anion-exchange material from the high-salt evaporator bottoms solutions--an effect which has not been duplicated using simple salt solutions. Similar behavior is observed for its lanthanide homologue, Nd(III), in complex evaporator bottoms surrogate solutions. There appears to be no single controlling factor--acid concentration, total nitrate concentration or solution ionic strength--which accounts for the approximately 2-fold increase in retention of the trivalent ions from complex solutions relative to simple solutions. Calculation of species activities (i.e., water, proton and nitrate) in such concentrated mixed salt solutions is difficult and of questionable accuracy, but it is likely that the answer to forcing formation of anionic nitrate complexes of americium lies in the relative activities of water and nitrate. From a practical viewpoint, the modest americium removal needs (ca. 50--75%) from nitric acid evaporator bottoms allow sufficient latitude for the use of non-optimized conditions such as running existing columns filled with older, well-used Reillex HPQ. Newer materials, such as HPQ-100 and the experimental bifunctional resins, which exhibit higher distribution coefficients, would allow for either increased Am removal or the use of smaller columns. It is also of interest that one of the experimental neutral-donor solid-support extractants, DHDECMP, exhibits a similarly high level of americium (total alpha) removal from EV bottoms and is much less sensitive to total acid content than commercially-available material

  12. Mechanism of gold dissolving in alkaline thiourea solution

    Institute of Scientific and Technical Information of China (English)

    CHAI Li-yuan; WANG Yun-yan

    2007-01-01

    Reaction mechanism of gold dissolving in alkaline thiourea solution was studied by electrochemical methods, such as cyclic voltammetry, chronopotentiometry, AC impedance, linear sweep voltammetry. Apparent activation energy of anodic process of gold electrode dissolving in alkaline thiourea solution is 14.91 kJ/mol. Rate determining step is the process of gold thiourea complex diffusing away from electrode surface to solution. The results of AC impedance and chronopotentiometry indicate that thiourea adsorbs on gold electrode surface before dissolving in solution. There does not exist proceeding chemical reactions. Formamidine disulfide, the decomposed product of thiourea, does not participate the process of gold dissolution and thiourea complex. Species with electro-activity produced in the process of electrode reaction adsorbs on the electrode surface. In alkaline thiourea solution, gold dissolving mechanism undergoes the following courses: adsorption of thiourea on electrode surface; charge transfer from gold atom to thiourea molecule; Au[SC(NH2)2]ads+ receiving a thiourea molecule and forming stable Au[SC(NH2)2]2+; and then Au[SC(NH2)2]2+diffusing away from the electrode surface to solution, the last step is the rate-determining one.

  13. Salt-specific effects in lysozyme solutions

    Directory of Open Access Journals (Sweden)

    T. Janc

    2016-03-01

    Full Text Available The effects of additions of low-molecular-mass salts on the properties of aqueous lysozyme solutions are examined by using the cloud-point temperature, T_{cloud}, measurements. Mixtures of protein, buffer, and simple salt in water are studied at pH=6.8 (phosphate buffer and pH=4.6 (acetate buffer. We show that an addition of buffer in the amount above I_{buffer} = 0.6 mol dm^{-3} does not affect the T_{cloud} values. However, by replacing a certain amount of the buffer electrolyte by another salt, keeping the total ionic strength constant, we can significantly change the cloud-point temperature. All the salts de-stabilize the solution and the magnitude of the effect depends on the nature of the salt. Experimental results are analyzed within the framework of the one-component model, which treats the protein-protein interaction as highly directional and of short-range. We use this approach to predict the second virial coefficients, and liquid-liquid phase diagrams under conditions, where T_{cloud} is determined experimentally.

  14. SIMULATION AND OPTIMIZATION OF TIMBER ALKALINE PULPING PROCESS IN PRESENCE OF SALTS OF SOME METALS HAVING MIXED VALENCE

    OpenAIRE

    I. Karpunin

    2012-01-01

    Process of alkaline pulping in the presence of salts of some metals having mixed valence has been simulated on the basis of the executed investigations. The paper reveals that optimization of alkaline (sulphate) pulping depends on chemical nature and metal and its amount which is introduced in the form of salt.

  15. SIMULATION AND OPTIMIZATION OF TIMBER ALKALINE PULPING PROCESS IN PRESENCE OF SALTS OF SOME METALS HAVING MIXED VALENCE

    Directory of Open Access Journals (Sweden)

    I. Karpunin

    2012-01-01

    Full Text Available Process of alkaline pulping in the presence of salts of some metals having mixed valence has been simulated on the basis of the executed investigations. The paper reveals that optimization of alkaline (sulphate pulping depends on chemical nature and metal and its amount which is introduced in the form of salt.

  16. A new electrochemical oscillatory system of bromate in alkaline solution

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A new electrochemical oscillatory system of bromate in alkaline solution is reported. In PtBromate-Alkaline solution system, two different types of electrochemical oscillations (Type Ⅰ and Type Ⅱ) can be observed. Type Ⅰ appears before hydrogen evolution and Type Ⅱ involves periodic hydrogen evolution. Type Ⅰ relates to the adsorption/desorption of the hydrogen on platinum electrode, and Type Ⅱ with periodic oscillation stems from the coupling of electrochemical reactions (the reduction of bromate and evolution hydrogen reaction) with mass transfer (diffusion and convection). More over, under the right conditions, the two types appear in different oscillatory modes, for example,simple periodical mode and mixed one, etc,, Crossed cycle in the cyclic voltammograms, which is the basiccharacteristics for electrochemical oscillatory systems, has also been observed as expected.

  17. Mechanism of zinc electroplating in alkaline zincate solution

    Institute of Scientific and Technical Information of China (English)

    PENG Wen-jie; WANG Yun-yan

    2007-01-01

    The cathodic deposition properties and mechanism of Zn in alkaline zincate solution were studied by electrochemical techniques. The results show that Zn2+ exists in the alkaline solution in the form of Zn(OH)42-. The apparent activation energy of the electrode reaction is 38.93 kJ/mol, which indicates that the discharge of Zn(OH)42- on cathode is controlled by electrochemical polarization, and accompanied by a preceding chemical reaction. The diflusion coefficient of Zn(OH)42- is 2.452×10~cm2/s. Zn(OH)2 is the species directly discharged on the cathode surface. Based on the above results the mechanism of zinc electroplating in alkaline zincate solution was put forward.The discharged species is Zn(OH)2 formed from the preceding chemical reaction, which becomes Zn(OH)ad when gaining one electron, and then gaining the second electron to become Zn.The first electron gaining step is rate determining one.

  18. SOLUTION MINING IN SALT DOMES OF THE GULF COAST EMBAYMENT

    Energy Technology Data Exchange (ETDEWEB)

    Griswold, G. B.

    1981-02-01

    Following a description of salt resources in the salt domes of the gulf coast embayment, mining, particularly solution mining, is described. A scenario is constructed which could lead to release of radioactive waste stored in a salt dome via inadvertent solution mining and the consequences of this scenario are analyzed.

  19. Apparent Dissolution Kinetics of Diatomite in Alkaline Solution

    Institute of Scientific and Technical Information of China (English)

    DU Gaoxiang; L(U) Guocheng; HE Xuwen

    2013-01-01

    The dissolution kinetics of diatomite in alkaline solution is the theoretical basis for the process optimization of alkali-diatomite reaction and its applications.In this study,the dissolution kinetics of diatomite in NaOH solution is investigated.The results indicate that the dissolution reaction fits well the unreacted shrinking core model for solid-liquid heterogeneous reactions.The apparent reaction order for NaOH is 2 and the apparent activation energy for the reaction (Ea) is 28.06 kJ.mol-1.The intra-particle diffusion through the sodium silicate layer is the rate-controlling step.When the dissolution reaction occurs at the interface of unreacted diatomite solid core,the diffusion in the trans-layer (the liquid film around the wetted particle) reduces the rate of whole dissolution process.

  20. Corrosion of silicon nitride in high temperature alkaline solutions

    Science.gov (United States)

    Qiu, Liyan; Guzonas, Dave A.; Qian, Jing

    2016-08-01

    The corrosion of silicon nitride (Si3N4) in alkaline solutions was studied at temperatures from 60 to 300 °C. Si3N4 experienced significant corrosion above 100 °C. The release rates of silicon and nitrogen follow zero order reaction kinetics and increase with increasing temperature. The molar ratio of dissolved silicon and nitrogen species in the high temperature solutions is the same as that in the solid phase (congruent dissolution). The activation energy for silicon and nitrogen release rates is 75 kJ/mol which agrees well with that of silica dissolution. At 300 °C, the release of aluminum is observed and follows first order reaction kinetics while other minor constituents including Ti and Y are highly enriched on the corrosion films due to the low solubility of their oxides.

  1. Detection of ampicillin, its sodium salt and alkaline hydrolysis products by MALDI-TOF Mass Spectrometry

    Directory of Open Access Journals (Sweden)

    Lukáš Hleba

    2016-05-01

    Full Text Available Antibiotic resistance of bacteria is very big problem in clinical and veterinary medicine in recent year. This problem is increasing by the exposure of bacteria against antibiotics. The most spread of resistance is resistance against penicillins antibiotics. Ampicillin is common use antibiotic in the both medicine. Therefore, detection of antibiotics and antibiotic resistance are very important for prevention of spread of antibiotics in the environment and resistant bacteria too. Therefore the aim of this study was detection of ampicillin, its sodium salts and alkaline hydrolysis products by MALDI-TOF Mass Spectrometry. For detection of pure ampicillin, its sodium salts and alkaline hydrolysed products MALDI-TOF MS (Matrix Assisted Light Desorption Ionization – Time of Flight Mass Spectrometry Microflex LT in positive ion mode was used. Determined mass spectra were observed by FlexAnalysis software. The mass spectra and molecular weight of ampicillin, its sodium salts and hydrolysed products were compared with theoretical molecular weight of these compounds. The results showed that its possible to detect ampicillin, its sodium salts and hydrolyzed products by MALDI-TOF MS in positive ion mode with some correction in analytical software. This knowledge is resulting that MALDI-TOF MS detection method can be useful for detection of ampicillin from different kind of environment samples and its possible to detect ampicillin resistance mechanism (enzymatic destruction indirectly, because resistance against penicillins is enzymatic hydrolysis of beta-lactam core. Also the most important issue is that method is very quickly and cheap.

  2. Optimization of salt concentration in PEG-based crystallization solutions

    OpenAIRE

    Yamanaka, Mari; Inaka, Koji; Furubayashi, Naoki; Matsushima, Masaaki; Takahashi, Sachiko; Tanaka, Hiroaki; Sano, Satoshi; Sato, Masaru; Kobayashi, Tomoyuki; Tanaka, Tetsuo

    2010-01-01

    Although polyethylene glycol (PEG) is the most widely used precipitant in protein crystallization, the concentration of co-existing salt in the solution has not been well discussed. To determine the optimum salt concentration range, several kinds of protein were crystallized in a 30% PEG 4000 solution at various NaCl concentrations with various pH levels. It was found that, if crystallization occurred, the lowest effective salt concentration depended on the pH of the protein solution and the ...

  3. Zinc electrodeposition from alkaline zincate solution by pulsating overpotentials

    Directory of Open Access Journals (Sweden)

    MILOS V. SIMICIC

    2000-09-01

    Full Text Available It is well known that smooth zinc deposits cannot be obtained from alkaline zincate using constant overpotential and current rate. During prolonged metal deposition, spongy and dendritic deposits are formed. It has been shown that the deposits are less agglomerated in the case of square-wave pulsating overpotentials regime than the ones obtained in case of constant overpotential regime. This is explained in a semiquantitative way by two phenomena: selective anodic dissolution during overpotentials “off” period and decreasing diffusion control. These effects is more pronounced at higher pause-to-pulse ratio. Increasing the pause-to-pulse ratio causes a reduction of the ratio between diffusion and activation overpotential, resulting in a more compact deposit. Confirmation of the proposed semiquantitative mathematical model was obtained by zinc electrodeposition onto a copper wire from a 0.1 M zincate solution in 1.0 M KOH at room temperature.

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

    Science.gov (United States)

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

    2015-05-28

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

  5. The autoreduction of pertechnetate in aqueous, alkaline solutions

    International Nuclear Information System (INIS)

    The autoreduction of pertechnetate (99TcO4-) to Tc(IV/V) alkoxide complexes in aqueous, alkaline, solutions is described. Solutions of sodium pertechnetate (0.01M) reacted with nitrogen and oxygen donor ligands (1.0M) in 2M sodium hydroxide. Solutions containing nitrogen donor ligands (e.g., EDTA) showed the initial formation of lightly colored complexes followed by rapid decomposition in air. In contrast, stable, reduced complexes were formed within minutes of mixing pertechnetate with mono- and disaccharides in strong base, as indicated by a persistent color change. Chemical yields of these reactions were determined by thin layer chromatography or paper chromatography and radiochemically assayed with a Bioscan imaging scanner. Analysis by UV-vis spectroscopy suggested that Tc(IV) or Tc(V) complexes were produced, with the oxidation state dependent on the reducing ligand. These experiments may help explain the reduction of pertechnetate to the soluble complexes that have been found in the Hanford nuclear waste tanks. (author)

  6. The effect of acrylic comonomers on the hydrolytic stability of polyacrylamides at high temperature in alkaline solution

    Energy Technology Data Exchange (ETDEWEB)

    Dexter, R.W.; Ryles, R.G.

    1988-05-01

    A major cause of instability in acrylamide-based polymers used in tertiary oil recovery is hydrolysis of the amide groups, especially at alkaline pH and high temperatures. Changes in polymer composition resulting from hydrolysis can cause precipitation from sea-water solutions. This work has studied the effects of the sodium salts of acrylic acid and acrylamidomethyl propane sulfonic acid (AMPS) on the rate of hydrolysis of acrylamide copolymers in alkaline solutions at high temperatures. Copolymers were prepared containing 0 - 50% of the anionic comonomers and hydrolyzed in aqueous solution at pH 8.5 at 90/sup 0/, 107/sup 0/, and 120/sup 0/C. The extent of hydrolysis was measured by a conductimetric method, analyzing for the total carboxylate content. It was found that the rate of hydrolysis decreased as the mole ratio of either of the anionic comonomers increased and that AMPS was more effective in preventing hydrolysis at all of the temperatures studied.

  7. Indium and scandium extraction by benzene solutions of 1-phenyl-3-methyl-4-benzoylpyrazolon-5 in the presence of salts

    International Nuclear Information System (INIS)

    The extraction of indium and scandium with benzene solutions of 1-phenyl-3-methyl-4-benzoylpyrazolone-5 from solutions of salts of alkaline metals has been studied. The effect of the desalting electrolyte is determined by two factors: Sechenov parameters and complexing of the metal ion with the anions of the desalting salts. Equations describing the effect of the desalters are given. A relationship has been established between the Sechenov parameters characterizing the desalting capacity of the salts and the hydration of the latter. It has been confirmed that in the case of In3+ no intraspheric complexes with anions NO3- and ClO4- are present

  8. New sand consolidation technique using hot alkaline solutions: laboratory evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Moreno, F.E.; Rico, A.; Mendez, Z. [PDVSA-Intevep, Caracas (Venezuela); Materan, S. [Simon Bolivar Univ., Caracas (Venezuela)

    2002-06-01

    Some well known problems in the petroleum industry are related to sanding problems caused by pressure falls, friction and dissolution of minerals during steam injection. The prospect of using hot alkaline solutions to achieve sand consolidation was investigated in this paper. Experimental work was performed using Venezuelan sand samples (S-1, S-2, and S-3) from various unconsolidated heavy oil reservoirs and commercial Silboca (S-4) sands to validate this new reservoir sand consolidation technique. A pressure of 500 pounds per square inch was applied to samples that had been packed into Teflon tubes and placed in a horizontal stainless steel cell. Following this, for a period varying from 2 to 5 hours, a hot sodium carbonate solution between 120 and 250 Celsius was injected. Every twenty minutes, the effluent solution was sampled. Before and after each run, permeability measurements were obtained to monitor the variations. Sand packs were dried at 100 Celsius after each test. An electron microscope was used to observe the morphology of secondary phases. For S-1 and S-2, sodium aluminium silicates were identified in the secondary phases for tests with temperature above 240 Celsius. In the case of S-3 and S-4, no consolidation was observed. The authors believe that large grain sizes and a 98 per cent quartz content respectively explain this phenomenon. It is suspected that sand consolidation requires the presence of aluminium contained in clays and/or feldspar. The critical parameters for sand consolidation were identified as temperature, pore volume, composition, and grain size. The process did not seem greatly affected by soaking time and injection rate. The advantages of this technique would be principally the minimization of sanding problems and reductions in the costs associated with production operations. 7 refs., 12 figs.

  9. Bedded salt in Ontario : geology, solution mining and cavern storage

    Energy Technology Data Exchange (ETDEWEB)

    Carter, T. [Ontario Ministry of Natural Resources, London, ON (Canada). Petroleum Resources Centre

    2009-07-01

    This presentation discussed bedded salt geology in Ontario in relation to cavern storage and solution mining. Ontario's salt basin forms part of the Michigan basin. The salt formed as reefs surrounding the shallow basin restricted the flow of water. Salt then formed as the water evaporated. The bedded salt occurs in several layers underlying up to 16,000 km{sup 2} in the province. Subsurface resources used in the area include salt cavern hydrocarbon storage; oil and gas reservoirs; and natural gas reservoir storage. The Salina Group stratigraphy is comprised of several separate salt beds with a maximum combined thickness of 90 m. The Salina salt beds exhibit evidence of dissolution after deposition. There are currently 20 active solution mining wells in operation in the Windsor and Goderich regions. There are currently 112 wells and 70 caverns used for cavern storage in Ontario that are used to store approximately 27 million bbl of liquefied petroleum gas (LPG) and oil. Non-salt layers in the salt beds can interfere with both solution mining and cavern storage operations. tabs., figs.

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

    Directory of Open Access Journals (Sweden)

    Jan-Michael Y. Carrillo

    2014-07-01

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

  11. [Structure and Activity of Fungal Lipases in Bile Salt Solutions].

    Science.gov (United States)

    Bogdanova, L R; Bakirova, D R; Valiullina, Yu A; Idiyatullin, B Z; Faizullin, D A; Zueva, O S; Zuev, Yu F

    2016-01-01

    The changes in structure and catalytic properties of fungal lipases (Candida rugosa, Rhizomucor miehei, Mucor javanicus) were investigated in micellar solutions of bile salts that differ in hydrophilic-lypophilic balance and reaction medium properties. The methods of circular dichroism and tryptophan fluorescence were applied to estimate the changes in peptide structure within complexes with bile salt micelles. Bile salts do not exert a significant influence on the structure of the enzymes under study: in Rh. miehei and M. javanicus lipases the alpha helix content slightly decreased, the influence of bile salts on the C. rugosa structure was not revealed. Despite negligible structural modifications in the enzymes, in bile salt solutions a considerable change in their catalytic properties was observed: an abrupt decrease in catalytic effectiveness. Substrate-bile salts micelles complex formation was demonstrated by the NMR self-diffusion method. The model of a regulation of fungal lipase activity was proposed. PMID:27192825

  12. Preparing poly(aryl ethers) using alkaline earth metal carbonates, organic acid salts, and optionally copper compounds, as catalysts

    International Nuclear Information System (INIS)

    This patent describes an improved process for preparing poly(aryl ethers) and poly(aryl ether ketones) by the reaction of a mixture of at least one bisphenol and at least one dihalobenzenoid compound, and/or a halophenol. The improvement comprises providing to the reaction, a base which is a combination of an alkaline earth metal carbonate and/or bicarbonate and a potassium, rubidium, or cesium salt of an organic acid or combination of organic salts thereof

  13. Preparing poly(aryl ethers) using alkaline earth metal carbonates, organic acid salts, and optionally copper compounds, as catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Winslow, P.A.; Kelsey, D.R.; Matzner, M.

    1988-09-27

    This patent describes an improved process for preparing poly(aryl ethers) and poly(aryl ether ketones) by the reaction of a mixture of at least one bisphenol and at least one dihalobenzenoid compound, and/or a halophenol. The improvement comprises providing to the reaction, a base which is a combination of an alkaline earth metal carbonate and/or bicarbonate and a potassium, rubidium, or cesium salt of an organic acid or combination of organic salts thereof.

  14. IR studies of EDTA alkaline salts interaction with the surface of inorganic oxides

    Science.gov (United States)

    Ryczkowski, J.

    2005-10-01

    The adsorption of alkaline salts of ethylenediaminetetraacetic acid (EDTA) on inorganic supports characterized by the different value of the isoelectric point of the surface (IEPS) has been investigated by transmission and photoacoustic (PA) FT-IR. The IR spectra in the 1800-1200 cm -1 region of the supported complexones are different from those of the unsupported compounds. The results obtained imply that the observed changes in the properties of adsorbed complexones are mainly due to interaction of the carboxyl groups of chelate molecule with inorganic oxide hydroxyl groups. The models of those interactions have been proposed. The IEPS value has a noticeable influence on the nature of the interactions observed. Based on the experimental data the ability of inorganic oxide interaction with the chelate molecule can be presented as follows: V 2O 5 < SiO 2 < TiO 2 < MgO < Al 2O 3 < ZrO 2-La < ZrO 2.

  15. Solution-Derived Sodalite Made with Si- and Ge-Ethoxide Precursors for Immobilizing electrorefiner salt

    Energy Technology Data Exchange (ETDEWEB)

    Riley, Brian J.; Lepry, William C.; Crum, Jarrod V.

    2016-01-01

    Chlorosodalite has the general form of Na8(AlSiO4)6Cl2 and this paper describes experiments conducted to synthesize sodalite to immobilize a mixed chloride salt using solution-based techniques. Sodalites were made using different Group IV contributions from either Si(OC2H5)4 or Ge(OC2H5)4, NaAlO2, and a simulated spent electrorefiner salt solution containing a mixture of alkali, alkaline earth, and lanthanide chlorides. Additionally, 6 glass binders at low loadings of 5 mass% were evaluated as sintering aids for the consolidation process. The approach of using the organic Group IV additives can be used to produce large quantities of sodalite at room temperature and shows promise over a method where colloidal silica is used as the silica source. However, the small particle sizes inhibited densification during pressure-less sintering.

  16. Decomposition Studies of Triphenylboron, Diphenylborinic Acid and Phenylboric Acid in Aqueous Alkaline Solutions Containing Copper

    Energy Technology Data Exchange (ETDEWEB)

    Crawford, C.L. [Westinghouse Savannah River Company, AIKEN, SC (United States); Peterson, R. A.

    1997-02-11

    This report documents the copper-catalyzed chemical kinetics of triphenylboron, diphenylborinic acid and phenylboric acid (3PB, 2PB and PBA) in aqueous alkaline solution contained in carbon-steel vessels between 40 and 70 degrees C.

  17. PHYSICAL, MECHANICAL, AND DURABILITY PERFORMANCE OF GFRP SQUARE REINFORCING BARS EXPOSED TO ALKALINE SOLUTION

    OpenAIRE

    Ahmed H. Ali; Awad El hashimy; Hesham Haggag

    2015-01-01

    This paper presents an experimental study that investigated the mechanical, physical , and durability characterization of square glass fibre - reinforced polymer (GFRP) bars exposed to alkaline solution. The GFRP square bars were exposed to alkaline solution at 22, 40, and 60°C to accelerate the effect of the concrete environment. The measured tensile strengths of the GFRP square bars before and after exposure were considered as a measure of ...

  18. Electrochemical study of benzene on Pt of various surface structures in alkaline and acidic solutions

    OpenAIRE

    Montilla Jiménez, Francisco; Morallón Núñez, Emilia; Vázquez Picó, José Luis

    2002-01-01

    The electrochemical behaviour of benzene on platinum electrodes (polycrystalline and single-crystal electrodes) has been studied in acidic and alkaline solutions. In acid solutions the reduction of benzene to cyclohexane takes place in all the platinum surface structure employed, however it does not occur in alkaline media (0.1 M NaOH). In this case, the hydrogen adsorption/desorption processes displace the adsorbed benzene from the electrode surface. The oxidation of benzene is also af...

  19. Methanol oxidation on Pd/Pt(poly) in alkaline solution

    Science.gov (United States)

    Maksic, A.; Rakocevic, Z.; Smiljanic, M.; Nenadovic, M.; Strbac, S.

    2015-01-01

    Bimetallic electrodes prepared by Pd nanoislands spontaneously deposited on polycrystalline platinum, Pt(poly), at submonolayer coverage were explored for methanol oxidation in alkaline media. Characterization of obtained Pd/Pt(poly) nanostructures was performed ex situ by AFM imaging, spectroscopic ellipsometry and by X-ray photoelectron spectroscopy. In situ characterization of the obtained electrodes and subsequent methanol oxidation measurements were performed by cyclic voltammetry in 0.1 M KOH. Platinum surface with 35% Pd coverage exhibited the highest catalytic activity for methanol oxidation in alkaline media, exceeding those of bare Pt and Pd. Both synergistic and electronic effects are responsible for such enhanced catalysis. The origin of the synergistic effect and possible reaction pathways for methanol oxidation were discussed taking into account the activity of obtained bimetallic electrodes for the oxidation of CO and formaldehyde, as the most probable reaction intermediates.

  20. The speciation of actinide ions in concentrated salt solutions

    International Nuclear Information System (INIS)

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

  1. Partitioning high-level waste from alkaline solution: A literature survey

    International Nuclear Information System (INIS)

    Most chemical partitioning procedures are designed for acidic feed solutions. However, the high-level waste solutions in the underground storage tanks at US Department of Energy defense production sites are alkaline. Effective partitioning procedures for alkaline solutions could decrease the need to acidify these solutions and to dissolve the solids in acid, which would simplify subsequent processing and decrease the generation of secondary waste. The author compiles candidate technologies from his review of the chemical literature, experience, and personal contacts. Several of these are recommended for evaluation

  2. Screening of hydrodynamic interactions for polyelectrolytes in salt solution

    OpenAIRE

    Smiatek, Jens; Schmid, Friederike

    2008-01-01

    We provide numerical evidence that hydrodynamic interactions are screened for charged polymers in salt solution on time scales below the Zimm time. At very short times, a crossover to hydrodynamic behavior is observed. Our conclusions are drawn from extensive coarse-grained computer simulations of polyelectrolytes in explicit solvent and explicit salt, and discussed in terms of analytical arguments based on the Debye-Hueckel approximation.

  3. Solution, thermal and optical properties of bis(pyridinium salt)s as ionic liquids

    International Nuclear Information System (INIS)

    Bis(pyridinium salt)s containing different alkyl chain lengths and various organic counterions were prepared by the ring-transmutation reaction of bis(pyrylium tosylate) with aliphatic amines in dimethyl sulfoxide at 130–135 °C for 18 h and their tosylate counterions were exchanged to other anions such as triflimide, methyl orange, and dioctyl sulfosuccinate by the metathesis reaction in a common organic solvent. Their chemical structures were established by using 1H, 19F, and 13C NMR spectra. The thermal properties of bis(pyridinium salt)s were studied by DSC and TGA measurements. Some of the dicationic salts provided low melting points below 100 °C and some of them displayed amorphous properties. Polarized optical microscopy studies revealed the crystal structures prior to melting temperatures in some cases. Their optical properties were examined by using UV–Vis and photoluminescent spectrometers; and they emitted blue light both in the solution and solid states regardless of their microstructures, counterions, and the polarity of organic solvents. However, most of these salts exhibited hypsochromic shifts in their emission peaks in the solid state when compared with those of their solution spectra. Due to unique properties of methyl orange anion as a pH indicator, two of the salts showed different color change in varying concentrations of triflic acid in common organic solvents, demonstrating their potential use as an acid sensor in methanol, acetonitrile and acetone. Highlights: ► Luminescent dicationic salts were synthesized by ring-transmutation and metathesis reactions. ► Thermal and optical properties of dicationic salts are affected by the size of anion structures. ► Due to the methyl orange counterions, some dicationic salts showed pH- sensing property

  4. Methane absorption and application of mixed organic aggregate prepared from Span80 and alkaline salt

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The water-based materials for mine gas absorption and explosion suppression were prepared, in which the mixed organic aggregate of Span80 and alkaline salt can be used as methane absorbent. Methane was used as a model of mine gas, and the absorptions of methane with different complex materials were studied using head space gas chromatography. Then the state of aqueous material was characterized with laser light scattering instrument and the effects of different complex materials on explosion suppression were preliminarily studied in explosion chamber which can simulate mine gas explosion. The research results showed that complex material could absorb methane and there was some corre- lation between the mean diameter of organic aggregate in aqueous material and the absorption effect. Additionally, the aqueous material could suppress the methane explosion to some degree. The material can absorb mine gas in atomization condition, therefore, degrease mine gas concentration and influence the distribution of mine gas in the space, and then suppress the mine gas explosion to some extent.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2005-09-26

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

  6. Technetium removal column flow testing with alkaline, high salt, radioactive tank waste

    International Nuclear Information System (INIS)

    This report describes two bench-scale column tests conducted to demonstrate the removal of Tc-99 from actual alkaline high salt radioactive waste. The waste used as feed for these tests was obtained from the Hanford double shell tank AW-101, which contains double shell slurry feed (DSSF). The tank sample was diluted to approximately 5 M Na with water, and most of the Cs-137 was removed using crystalline silicotitanates. The tests were conducted with two small columns connected in series, containing, 10 mL of either a sorbent, ABEC 5000 (Eichrom Industries, Inc.), or an anion exchanger Reillex trademark-HPQ (Reilly Industries, Inc.). Both materials are selective for pertechnetate anion (TcO4-). The process steps generally followed those expected in a full-scale process and included (1) resin conditioning, (2) loading, (3) caustic wash to remove residual feed and prevent the precipitation of Al(OH)3, and (4) elution. A small amount of Tc-99m tracer was added as ammonium pertechnetate to the feed and a portable GEA counter was used to closely monitor the process. Analyses of the Tc-99 in the waste was performed using ICP-MS with spot checks using radiochemical analysis. Technetium x-ray absorption spectroscopy (XAS) spectra of 6 samples were also collected to determine the prevalence of non-pertechnetate species [e.g. Tc(IV)

  7. Metal-carbonate formation from ammonia solution by addition of metal salts - An effective method for CO2 capture from landfill gas (LFG)

    International Nuclear Information System (INIS)

    The absorption of CO2 from LFG in different weight concentration ammonia solution and metal salts (Zinc and Barium) is investigated in this study. Addition of metal salts results in useful metal carbonates when LFG is passed through the solution. Barium salts show a better potential of removing CO2 as compared to Zinc salts. Addition of Barium salts to ammonia solution results in a new absorbent as no study has been focused on it till date. Also metal salts are added to alkaline wastewater which not only decreases the pH of the wastewater but also useful metal carbonates are obtained from wastewater when LFG is passed through it. Different parameters like CO2 loading, reaction rate and change in pH are investigated. Formation of carbonates is proved by using SEM and XRD analysis. Raman spectroscopy was performed on the discarded liquid after removal of carbonates to understand the formation of bicarbonates, carbonates and carbamates. (author)

  8. Anodic dissolution of gold in alkaline solutions containing thiourea, thiosulfate and sulfite ions

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Gold dissolves electrochemically in alkaline solutions containing ligands to form complex ions with gold ion. Therefore, selective leaching of noble metals is expected without dissolution of base metals such as steels, aluminum alloys in scrap treatment. Gold electrodes were investigated using linear sweep voltammetry, EQCM method and potentiostatic electrolysis in alkaline solutions containing thiourea, Na2SO3 and Na2S2O3. The solution composition, electrode potential affect gold dissolution rate and current efficiency. The gold dissolved from anode electrode forms complex ions, suspension particles as compound precipitates and deposits on cathode electrode as a metal. Anodic efficiency for gold dissolution is between 10% and 22%. This is caused by the oxidation decomposition of sulfite ions and thiourea. The stability of the alkaline solution containing these elements was also estimated by capillary electrophoresis technique.

  9. Mass spectra of alkaline earth salts with a FAB source. Complexation with crown ethers

    International Nuclear Information System (INIS)

    With a liquid desorption FAB source it is possible to obtain alkaline earth metal ions complexed by a crown ether. Conditions for formation of these complexes ions are examined for selection of the complexing agent in function of cation size. Behaviour of alkaline and alkaline earth compounds are compared allowing the differentiation of ion extraction phenomena by liquid desorption ion source and solvent extraction

  10. Structural behavior of progressively mined solution cavities in salt

    International Nuclear Information System (INIS)

    The stress field and the time dependent deformation around a solution cavity in rock salt are shown to be sensitive to the details of the excavation process and to the prevailing tectonic stress field. An analysis procedure is developing whereby an incremental excavation procedure and a creep routine are incorporated simultaneously into an axisymmetric finite element code

  11. 21 CFR 864.2875 - Balanced salt solutions or formulations.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Balanced salt solutions or formulations. 864.2875 Section 864.2875 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES HEMATOLOGY AND PATHOLOGY DEVICES Cell And Tissue Culture Products §...

  12. Anion exchange sorption of molybdate and germanate from salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Kislinskaya, G.E.; Denisova, T.I.; Sheka, I.A. (AN Ukrainskoj SSR, Kiev. Inst. Obshchej i Neorganicheskoj Khimii)

    1983-02-01

    A study has been made of the state of Mo(6) and Ge(4) in solutions containing various concentrations (5-300 g/l) of HCl and their sorption with highly-alkaline macroporous anionites (Duolite 101 D, ChFO, AM, AMP) and hydroxides of iron and aluminium, depending on pH value, element concentration and time of solution contact with sorbent. Polymer anions of molybdate with a sorption maximum at pH=1-3 and monomer anions of germanate at pH>8 are found to be the most active forms of molybdenum and germanium, as to their sorption, at their concentrations of 10/sup -6/-10/sup -5/g-atom/l in sodium chloride solutions. Regions of molybdate and germanate effective sorption with anionites and hydroxides of iron and aluminium in electrolyte solutions get narrower, as compared with aqueous solutions, due to competing sorption of a background electrolyte anion.

  13. Laser-induced breakdown spectroscopy for analysis of frozen salt solutions under Martian conditions

    Science.gov (United States)

    Schröder, Susanne; Pavlov, Sergey; Hübers, Heinz-Wilhelm; Rauschenbach, Isabelle; Jessberger, Elmar K.

    focusing on the major elemental composition as well as on minor elements. In general, the alkali metal and alkaline earth metal elements were clearly detectable in the LIBS spectra in the 280-900 nm region. This allowed for a good distinction between different frozen solutions. Also the oxygen and hydrogen lines gave good signal-to-noise ratios. On the other hand, in particular, sulphur, as known, is difficult to detect in this spectral range as only weak sulphur lines are apparent in this region. The experiments demonstrate the capability of LIBS for detection and identification of frozen salt solutions under Martian conditions.

  14. Analysis of frozen salt solutions with laser-induced breakdown spectroscopy under Martian conditions

    Science.gov (United States)

    Schröder, S.; Pavlov, S. G.; Hübers, H.-W.; Rauschenbach, I.; Jessberger, E. K.

    2010-05-01

    focusing on the major elemental composition as well as on minor elements. In general, the alkali metal and alkaline earth metal elements were clearly detectable in the LIBS spectra in the 280-900 nm region. This allowed for a good distinction between different frozen solutions. Also the oxygen and hydrogen lines gave good signal-to-noise ratios. On the other hand, in particular, sulphur, as known, is difficult to detect in this spectral range as only weak sulphur lines are apparent in this region. The experiments demonstrate the capability of LIBS for detection and identification of frozen salt solutions under Martian conditions.

  15. Methylene blue adsorption of GMZ bentonite and the effect of hyper-alkaline solution erosion

    International Nuclear Information System (INIS)

    The method of combining the halo method with the spectrometer method, was used to study on the Methylene blue (MB) adsorption of Gaomiaozi (GMZ) bentonite, which had been eroded by hyper-alkaline solution, to investigate the mechanism of the effect of hyper-alkaline pore water on the buffer/backfill properties of GMZ bentonite. Results present, method employed in this article is brief and feasible, and high accuracy; The total specific surface area calculated by the test of MB adsorption is more accurate than the method of ethylene glycol monomethyl ether (EGIVIE). The MB adsorption of samples, which had been eroded by hyper-alkaline solution, decreases with the increase of the concentration of hyper-alkaline solution, and the change law agrees with the variation of the mass percentage of montmorillonite in bentonite tested by X- Ray diffraction (XRD). Therefore, the erosion of hyper-alkaline pore water might dissolve montmorillonite, which is the effective composition of bentonite, and destroy the tetrahedron- octahedron-tetrahedron (T-O-T) structure of montmorillonite, then lead to the decrease of cation exchange capability and the specific surface area of montmorillonite, and the the macroscopic expressions are the decrease of MB adsorption, the swelling potential and the increase of permeability. (authors)

  16. Preliminary study on lithium-salt aqueous solution blanket

    International Nuclear Information System (INIS)

    Aqueous solution blanket using lithium salts such as LiNO3 and LiOH have been studied in the US-TIBER program and ITER conceptual design activity. In the JAERI/LANL collaboration program for the joint operation of TSTA (Tritium Systems Test Assembly), preliminary design work of blanket tritium system for lithium ceramic blanket, aqueous solution blanket and liquid metal blanket, have been performed to investigate technical feasibility of tritium demonstration tests using the TSTA. Detail study of the aqueous solution blanket concept have not been performed in the Japanese fusion program, so that this study was carried out to investigate features of its concept and to evaluated its technical problems. The following are the major items studied in the present work: (i) Neutronics of tritium breeding ratio and shielding performance Lithium concentration, Li-60 enrichment, beryllium or lead, composition of structural material/beryllium/solution, heavy water, different lithium-salts (ii) Physicochemical properties of salts Solubility, corrosion characteristics and compatibility with structural materials, radiolysis (iii) Estimation of radiolysis in ITER aqueous solution blanket. (author)

  17. The redox speciation of neptunium in acidic and alkaline solutions

    International Nuclear Information System (INIS)

    Newly developed in situ capabilities at the Advanced Photon Source have been used to obtain X-ray absorption spectroscopy (XAS) data from Np in aqueous solutions. L-edge XAS data have been obtained from acidic solutions in which Np was electrochemically stabilised in the (III) to (VI) states. A purpose-built electrochemical cell housed in appropriate safety containment allows the acquisition of XAS data while the solution is maintained under controlled applied potentials. This electrochemical cell has been used in a proof-of-concept experiment designed to demonstrate the use of X-ray absorption near-edge structural (XANES) data for the determination of thermodynamic formal potentials. XANES data were obtained at a series of applied potentials from a 1 M perchloric acid solution containing 5 mm Np. The relative concentrations of Np redox species as a function of applied potential were extracted from the data using principal component (factor) analyses. The formal potentials determined for the Np(VI)/Np(V) and Np(IV)/Np(III) couples agree with those previously published. Extended X-ray absorption fine structure (EXAFS) data were obtained from the same solution, held at potentials chosen to optimise the concentration of a single Np redox species. These data have been used to verify the co-ordination environment of Np ions as a function of oxidation state. Density functional theory (DFT), simple geometric modelling and results from the EXAFS data analysis are in agreement for the co-ordination environment of Np(III). In a related set of experiments, L-edge XAS data of Np(V), Np(VI) and Np(VII) were obtained from a basic solution. The Np oxidation state was varied by sparging the solution with ozone. Data were collected as the sample was sparged and also after the sparging gas was turned off. Np optical data were obtained in the same XAS cell and confirm the oxidation of Np(VI) to hepta-valent Np. The concentration of Np(VII) was determined using trivalent Cr as a

  18. Pulse radiolysis of tetraalkylammonium hydroxides in alkaline solution containing oxygen

    International Nuclear Information System (INIS)

    In the pulse radiolysis of aqueous oxygenated solutions of tetraalkylammonium hydroxides there is a build-up of ozonide ion lasting up to 100 μs after the pulse. The build-up does not occur in solutions containing a twenty fold (reactivity) excess of N2O to O2. The influence of various concentrations of tetraalkylammonium cations, oxygen and different reactivity ratios of N2O to O2 on the build-up of ozonide ion after the pulse was investigated. The reaction rates of O2-and O- with peroxy radicals and organic cations, respectively, control the nature of the observed build-up and decay of ozonide ion. (author)

  19. Radiolysis of capric acid in an alkaline nitrate solution

    International Nuclear Information System (INIS)

    Effect of absorbed dose of γ-radiation on radiation chemical yields of n-capric acid (CA) loss in nitrate-caustic solutions (0.52 mol/l of NaNO3, 0.24 mol/l NaOH, 0.02 mol/l Na2CO3) modelling composition of liquid radioactive wastes has been studied. Initial yield of decomposition of CA consists of 27 molecule/100 eV. Circuit of radiation-chemical degradation of CA by chain mechanism is justified. Reduction of decomposition of CA under irradiation of the solution in the presence of sandy-clay geological formation from injection well of underground waste disposal has been revealed

  20. Solid / solution interaction: The effect of carbonate alkalinity on adsorbed thorium

    Science.gov (United States)

    LaFlamme, Brian D.; Murray, James W.

    1987-02-01

    Elevated activities of dissolved Th have been found in Soap Lake, an alkaline lake in Eastern Washington. Dissolved 232Th ranges from less than 0.001 to 4.9 dpm/L compared to about 1.3 × 10 -5 dpm/ L in sea water. The enhanced activity in the lake coincides with an increase in carbonate alkalinity. Experiments were conducted to evaluate the effect of pH, ionic strength and carbonate alkalinity on Th adsorption on goethite. Thorium (10 -13 M total) in the presence of 5.22 mg/L α-FeOOH and 0.1 M NaNO 3 has an adsorption edge from pH 2-5. At pH 9.0 ± 0.6 the percent Th absorbed on the solid began to decrease from 100% at 100 meq/L carbonate alkalinity and exhibited no adsorption above 300 meq/L. The experimental data were modeled to obtain the intrinsic adsorption equilibrium constants for Th hydrolysis species. These adsorption constants were incorporated in the model to interpret the observed effect of carbonate alkalinity on Th adsorption. There are two main effects of the alkalinity. To a significant degree the decrease in Th adsorption is due to competition of HCO -3 and CO 2-3 ions for surface sites. Dissolved Th carbonate complexes also contribute to the increase of Th in solution.

  1. Photoionization of Sodium Salt Solutions in a Liquid Jet

    International Nuclear Information System (INIS)

    A liquid microjet was employed to examine the gas/liquid interface of aqueous sodium halide (Na+X-, X=Cl, Br, I) salt solutions. Laser excitation at 193 nm produced and removed cations of the form H+(H2O)n and Na+(H2O)m from liquid jet surfaces containing either NaCl, NaBr or NaI. The protonated water cluster yield varied inversely with increasing salt concentration, while the solvated sodium ion cluster yield varied by anion type. The distribution of H+(H2O)n at low salt concentration is identical to that observed from low-energy electron irradiated amorphous ice and the production of these clusters can be accounted for using a localized ionization/Coulomb expulsion model. Production of Na+(H2O)m is not accounted for by this model but requires ionization of solvation shell waters and a contact ion/Coulomb expulsion mechanism. The reduced yields of Na+(H2O)m from high concentration (10-2 and 10-1 M) NaBr and NaI solutions indicate a propensity for Br- and I- at the solution surfaces and interfaces. This is supported by the observation of multiphoton induced production and desorption of Br+ and I+ from the 10-2 and 10-1 M solution surfaces

  2. Photoionization of Sodium Salt Solutions in a Liquid Jet

    Energy Technology Data Exchange (ETDEWEB)

    Grieves, G. A.; Petrik, Nikolay G.; Herring-Captain, J.; Olanrewaju, B.; Aleksandrov, A.; Tonkyn, Russell G.; Barlow, Stephan E.; Kimmel, Gregory A.; Orlando, Thomas M.

    2008-06-05

    A liquid microjet was employed to examine the gas/liquid interface of aqueous sodium halide (Na+X-, X=Cl, Br, I) salt solutions. Laser excitation at 193 nm produced and removed cations of the form H+(H2O)n and Na+(H2O)m from liquid jet surfaces containing either NaCl, NaBr or NaI. The protonated water cluster yield varied inversely with increasing salt concentration, while the solvated sodium ion cluster yield varied by anion type. The distribution of H+(H2O)n at low salt concentration is identical to that observed from low-energy electron irradiated amorphous ice and the production of these clusters can be accounted for using a localized ionization/Coulomb expulsion model. Production of Na+(H2O)m is not accounted for by this model but requires ionization of solvation shell waters and a contact ion/Coulomb expulsion mechanism. The reduced yields of Na+(H2O)m from high concentration (10-2 and 10-1 M) NaBr and NaI solutions indicate a propensity for Br- and I- at the solution surfaces and interfaces. This is supported by the observation of multiphoton induced production and desorption of Br+ and I+ from the 10-2 and 10-1 M solution surfaces.

  3. Salt effect in radiolysis of frozen cyanocobalamine solutions

    International Nuclear Information System (INIS)

    Investigated has been radiolysis of aqueous solutions of cyanocobalamine (vitamin B-12) with 200 mg/l concentration, containing and not containing sodium chloride in the concentration of 0.9 weight % NaCl. The irradiation has been carried our using γ-installation (with the dose capacity 5 Mrad/hr) in sealed in the air glass ampoules at 18, 0, -11, -22, -50, -78 and 196 deg C. It has been shown that in the course of liquid phase radiolysis NaCl presence in the solution does not practicaly affect the degree of radiational decomposition of cyanocobalamine. At the temperature decrease strong effect of salt is detected in non-salt solution practically complete stabilization of cyanocobalamine is observed already at -11 deg C, whereas in the presence of salt close grade of protection is reached only at -78 deg C and does not change at the temperature decrease down to -196 deg C. The effect of cryostabilization can be accounted for by two reasons: the solution microstra-tification at freezing, so that in every separate phase there is mainly one of the system components and diffusion rate reduction of hydroxile radicals at temperature decrease

  4. Optical absorption of dilute solutions of metals in molten salts

    International Nuclear Information System (INIS)

    The F-centre model for the bound state and the first optical transition of an electron in a metal-molten salt solution is examined in the high dilution limit appropriate for comparison with optical absorption data. It is first argued that the model is consistent with recent neutron diffraction and computer simulation data on the structure of pure molten salts, and not incompatible with an Anderson localization model for the electronic conductivity of the solution at higher concentration of metal. A detailed evaluation of the model is presented for the case of a molten salt of equi-sized ions simulating molten KCl. The treatment of the electronic states is patterned after semicontinuum approximations previously applied to the F-centre in ionic crystals, but the equilibrium radius of the electronic cavity and its fluctuations are determined self-consistently from the free energy of the solution. The detailed analysis of this case and the agreement of the results with experiment allow the construction of a simple parametrization scheme, which is then applied to explore the trends of the optical absorption spectrum and of the volume of mixing through the whole family of M-MX solutions, where M is an alkali and X a halogen. Similarities and differences of the electronic bound state in the crystal and in the liquid are underlined. (author)

  5. CRITICALITY SAFETY OF PROCESSING SALT SOLUTION AT SRS

    Energy Technology Data Exchange (ETDEWEB)

    Stephens, K; Davoud Eghbali, D; Michelle Abney, M

    2008-01-15

    High level radioactive liquid waste generated as a result of the production of nuclear material for the United States defense program at the Savannah River Site has been stored as 36 million gallons in underground tanks. About ten percent of the waste volume is sludge, composed of insoluble metal hydroxides primarily hydroxides of Mn, Fe, Al, Hg, and most radionuclides including fission products. The remaining ninety percent of the waste volume is saltcake, composed of primarily sodium (nitrites, nitrates, and aluminates) and hydroxides. Saltcakes account for 30% of the radioactivity while the sludge accounts for 70% of the radioactivity. A pilot plant salt disposition processing system has been designed at the Savannah River Site for interim processing of salt solution and is composed of two facilities: the Actinide Removal Process Facility (ARPF) and the Modular Caustic Side Solvent Extraction Unit (MCU). Data from the pilot plant salt processing system will be used for future processing salt at a much higher rate in a new salt processing facility. Saltcake contains significant amounts of actinides, and other long-lived radioactive nuclides such as strontium and cesium that must be extracted prior to disposal as low level waste. The extracted radioactive nuclides will be mixed with the sludge from waste tanks and vitrified in another facility. Because of the presence of highly enriched uranium in the saltcake, there is a criticality concern associated with concentration and/or accumulation of fissionable material in the ARP and MCU.

  6. Acidizing carbonate reservoirs with chlorocarboxylic acid salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Richardson, E.A.; Scheuerman, R.F.; Templeton, C.C.

    1978-10-31

    A carbonate reservoir is acidized slowly by injecting an aqueous solution of a chlorocarboxylic acid salt so that the rate of the acidization is limited to the rate at which an acid is formed by the hydrolyzing of the chlorocarboxylate ions. The rate at which a chlorocarboxylic acid salt hydrolyzes to form an acid provides the desired rate of acid-release. A more complete acid-base reaction by chloroacetic acid, as compared to formic, acetic, and proprionic, is due to its being a much stronger acid. The pKa of chloroacetic acid is 2.86, whereas that of formic acid is 3.75, and that of acetic acid is 4.75. The pKa of a solution of a weak acid is the pH exhibited when the concentration of undissociated acid equals the concentration of the acid anion. 14 claims.

  7. Dual fluorescence of naphthylamines in alkaline aqueous solution

    Science.gov (United States)

    Ma, Li-Hua; Wen, Zhen-Chang; Lin, Li-Rong; Jiang, Yun-Bao

    2001-10-01

    Dual fluorescence was observed with N-(1-naphthyl)aminoacetate (1-NAA) in aqueous solution of pH 13.0 in the presence of cationic surfactants, cetyltrimethylammonium bromide (CTAB) and chloride (CTAC), below and after the critical micelle concentration (CMC). Similar dual fluorescence was also found with 1- and 2-naphthylamine (1-NA, 2-NA), N-(2-naphthyl)aminoacetate (2-NAA) and (1-naphthyl)ethylenediamine (1-NEDA), in the presence and absence of the cationic surfactants, but not with N, N-disubstituted 1- and 2-NAs. We concluded that the dual fluorescence was due to the excited-state deprotonation of the amino group in these NAs. The p Ka*s of the dual fluorescent NAs were estimated to be around 14 from the dual fluorescence pH titrations. No clear correlation was found for p Ka* with the amino substitution and the presence of cationic micelle.

  8. Enhanced oxygen evolution at hydrous oxy-hydroxide modified iron electrodes in aqueous alkaline solution

    OpenAIRE

    Lyons, Michael; Doyle, Richard

    2011-01-01

    Outstanding issues regarding the film formation and the oxygen evolution reaction (OER) electrocatalytic behaviour of multicycled iron oxyhydroxide films in aqueous alkaline solution have been revisited. The oxide is grown using a repetitive poltential multicycling technique, and the mechanism of the latter hydrous oxide formation process has been discussed. A duplex layer model of the oxide/solution interphase region is proposed. The acid/base behaviour of the hydrous oxide and the microdisp...

  9. Production of Reactor Fuel Oxides from Molten Chloride Salt Solutions

    International Nuclear Information System (INIS)

    Hanford Laboratories' work on reprocessing concepts for spent UO2-PuO2 fuels has led to the development of attractive, synthesis methods for several reactor fuel oxides possessing unique properties. By the use of molten chloride salt solutions as reaction media, it has been found possible to produce crystalline uranium and plutonium dioxides, and solid solutions of various oxide mixtures, at relatively low temperatures (500 to 750 deg. C). Exploratory work has indicated that these techniques may also be quite useful in the preparation of other nonmetallic fuel materials. Crystalline UO2 has been prepared by electrodeposition from molten chloride salt solutions of uranyl chloride. Material with oxygen-uranium ratios as low as 2.0006 and crystal densities as high as 10.92 (99.5% of the theoretical value) has been produced both in the laboratory and in 100-lb pilot-plant lots. This oxide appears well suited to such fuel element fabrication techniques as vibratory compaction. In carefully controlled laboratory-scale work, single crystals have been prepared weighing as much as 4 g. Conditions have also been worked out for the electro deposition of polycrystalline cylindrical UO2 rods. The intensive engineering studies have contributed markedly to the technology of containing and handling molten salts under chemical processing conditions and have provided a basis for preliminary cost studies which indicate that, with potential advances in technology, this method of preparation of dense UO2 may well compete economically with other established methods. Dense, black, finely divided crystals of UO2 with a bulk density greater than 6 g/cm3 have been produced by precipitation from molten salt media, under carefully selected conditions of salt composition, temperature, and sparge gas. It is anticipated that crystal growth can be controlled so as to give optimum particle-size distribution for fabrication of mixed oxide fuel elements. UO2-PuO2 and UO2-ThO2 solid solutions

  10. SODIUM ALUMINOSILICATE FOULING AND CLEANING OF DECONTAMINATED SALT SOLUTION COALESCERS

    International Nuclear Information System (INIS)

    During initial non-radioactive operations at the Modular Caustic Side Solvent Extraction Unit (MCU), the pressure drop across the decontaminated salt solution coalescer reached ∼10 psi while processing ∼1250 gallons of salt solution, indicating possible fouling or plugging of the coalescer. An analysis of the feed solution and the 'plugged coalescer' concluded that the plugging was due to sodium aluminosilicate solids. MCU personnel requested Savannah River National Laboratory (SRNL) to investigate the formation of the sodium aluminosilicate solids (NAS) and the impact of the solids on the decontaminated salt solution coalescer. Researchers performed developmental testing of the cleaning protocols with a bench-scale coalescer container 1-inch long segments of a new coalescer element fouled using simulant solution. In addition, the authors obtained a 'plugged' Decontaminated Salt Solution coalescer from non-radioactive testing in the MCU and cleaned it according to the proposed cleaning procedure. Conclusions from this testing include the following: (1) Testing with the bench-scale coalescer showed an increase in pressure drop from solid particles, but the increase was not as large as observed at MCU. (2) Cleaning the bench-scale coalescer with nitric acid reduced the pressure drop and removed a large amount of solid particles (11 g of bayerite if all aluminum is present in that form or 23 g of sodium aluminosilicate if all silicon is present in that form). (3) Based on analysis of the cleaning solutions from bench-scale test, the 'dirt capacity' of a 40 inch coalescer for the NAS solids tested is calculated as 450-950 grams. (4) Cleaning the full-scale coalescer with nitric acid reduced the pressure drop and removed a large amount of solid particles (60 g of aluminum and 5 g of silicon). (5) Piping holdup in the full-scale coalescer system caused the pH to differ from the target value. Comparable hold-up in the facility could lead to less effective cleaning and

  11. Some Corrosion Characteristics of Aged Aluminum Alloy 6061 in Neutral and Alkaline Solutions

    International Nuclear Information System (INIS)

    The composition and microstructure of the alloy as well as the corrosive nature of the environment play an important role in modifying the corrosion resistance of aluminum alloys. This work was intended to study the influence of the solution ph on the corrosion characteristics of 6061 aluminum alloy, (Al-Mg-Si alloy containing 0.22 wt % Cu) after aging at 225, 185 and 140 degree degree C for different periods of time. The investigation was performed by applying potentiodynamic polarization technique in neutral deaerated 0.5 % M NaCl solution as well as in alkaline NaOH solution (ph 10). Analysis of the potentiodynamic polarization curves showed similar dependence of Icorr and cathodic current densities on the aging treatment in both solutions. It was found that Ecorr values in the NaCl solution were shifted in the more noble direction while in the NaOH solution they were shifted in the more active direction compared to the solution treated condition. The magnitude of the noble or active shift in Ecorr increased with aging time for the under aged specimens and decreased towards Ecorr of the solution treated condition for the overaged specimens in both solutions. The Icorr values were higher in the alkaline solution for the same aging treatment

  12. Methanol synthesis using a catalyst combination of alkali or alkaline earth salts and reduced copper chromite for methanol synthesis

    Science.gov (United States)

    Tierney, John W.; Wender, Irving; Palekar, Vishwesh M.

    1993-01-01

    The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a catalyst combination comprising reduced copper chromite and basic alkali salts or alkaline earth salts. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100.degree.-160.degree. C. and the pressure range of 40-65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H.sub.2 /CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

  13. A study on the mechanism of stress corrosion cracking of duplex stainless steels in hot alkaline-sulfide solution

    Science.gov (United States)

    Chasse, Kevin Robert

    Duplex stainless steels (DSS) generally have superior strength and corrosion resistance as compared to most standard austenitic and ferritic stainless grades owing to a balanced microstructure of austenite and ferrite. As a result of having favorable properties, DSS have been selected for the construction of equipment in pulp and paper, chemical processing, nuclear, oil and gas as well as other industries. The use of DSS has been restricted in some cases because of stress corrosion cracking (SCC), which can initiate and grow in either the ferrite or austenite phase depending on the environment. Thorough understanding of SCC mechanisms of DSS in chloride- and hydrogen sulfide-containing solutions has been useful for material selection in many environments. However, understanding of SCC mechanisms of DSS in sulfide-containing caustic solutions is limited, which has restricted the capacity to optimize process and equipment design in pulp and paper environments. Process environments may contain different concentrations of hydroxide, sulfide, and chloride, altering corrosion and SCC susceptibility of each phase. Crack initiation and growth behavior will also change depending on the relative phase distribution and properties of austenite and ferrite. The role of microstructure and environment on the SCC of standard grade UNS S32205 and lean grade UNS S32101 in hot alkaline-sulfide solution were evaluated in this work using electrochemical, film characterization, mechanical testing, X-ray diffraction, and microscopy techniques. Microstructural aspects, which included residual stress state, phase distribution, phase ratio, and microhardness, were related to the propensity for SCC crack initiation in different simulated alkaline pulping liquors at 170 °C. Other grades of DSS and reference austenitic and superferritic grades of stainless steel were studied using exposure coupons for comparison to understand compositional effects and individual phase susceptibility

  14. The occurrence and origin of solutions in the Gorleben salt deposit

    International Nuclear Information System (INIS)

    In order to judge the usefulness of a salt deposit as a store for radioactive waste, it is necessary to examine the origin of all parts of the salt deposit. Only this scientific approach corresponds to the present state of geology. The article concerns the questions on the origin of the salt solutions found in the Gorleben salt deposit and the consequences from the occurrence of solutions in a salt deposit for final storage. (DG)

  15. Cast iron deterioration with time in various aqueous salt solutions

    Indian Academy of Sciences (India)

    Rita Mehra; Aditi Soni

    2002-02-01

    The changes with time in the corrosion rate and corrosion current density on a cast iron electrode in various aqueous salt solutions have been carried out using total immersion test and potentiostatic polarization curves. The concentration of salts taken is expected to be present in potable water. The relative behaviour of these salts towards corrosion has also been studied, which is found to be different from previous studies. The total immersion test parameters viz. weight loss, corrosion rate as well as potentiostatic parameters, open circuit potential, corr, Tafel slopes, corrosion rate, have been calculated by standard methods. Besides these the relative increase in corrosion rate with time as well as the percentage to which corrosion rate should be decreased so as to provide protection towards corrosion have also been calculated. It was found that KCl and NaCl are major contributors than MnSO4, Pb(NO3)2, KI and KBr. The relative increase in corrosion is high in KBr, KI, NaNO3, CaCl2, and less in Pb(NO3)2, NaHCO3 and CaCO3 test solutions. For the reliability of results the data has been statistically analysed.

  16. Characterization of actinides in simulated alkaline tank waste sludges and leach solutions

    International Nuclear Information System (INIS)

    Current plans call for an alkaline scrub of actinide-bearing sludges in the Hanford Waste tanks prior to their incorporation in glass waste forms. Though it is assumed that actinides will remain in the sludge phase during this procedure, this assumption is based on insufficient supporting thermodynamic and kinetic data. In this project the authors will investigate the fundamental chemistry of actinides in strongly alkaline solution and solid phases to strengthen the foundation and identify potential limitations of this approach. They will focus on the characterization of the leaching of actinides from simulated BiPO4, REDOX, and PUREX sludges, the identification of actinide mineral phases in the sludge simulants, and the possible solubilization of actinides by complexation and radiolysis effects. This program will provide new fundamental information on the chemical behavior and speciation of uranium, neptunium, plutonium, and americium in simulated alkaline tank waste sludges and alkaline scrub liquors. Sludge simulants will be prepared from the appropriate matrix components using published data for guidance. Actinide ions will be introduced in the oxidation states pertinent to process conditions. The authors will characterize the speciation of the actinides in the sludges using a variety of techniques. In parallel studies, they will address the chemistry of actinide ions in alkaline solutions, principally those containing chelating agents. The third critical element of this research will be to assess the impact of radiolysis on actinide behavior. By correlating actinide speciation in the solid and solution phases with sludge composition, it will be possible to predict conditions favoring mobilization (or immobilization) of actinide ions during sludge washing. The new information will increase predictability of actinide behavior during tank sludge washing, and so contribute to minimization of the volume of high level waste created

  17. Bioprecipitation of uranium from alkaline waste solutions using recombinant Deinococcus radiodurans

    International Nuclear Information System (INIS)

    Highlights: • Deinococcus radiodurans was genetically engineered to overexpress alkaline phosphatase (PhoK). • Deino-PhoK bioprecipitated U efficiently over a wide range of input U concentration. • A maximal loading of 10.7 g U/g of biomass at 10 mM input U was observed. • Radioresistance and U precipitation by Deino-PhoK remained unaffected by γ radiation. • Immobilization of Deino-PhoK facilitated easy separation of precipitated U. -- Abstract: Bioremediation of uranium (U) from alkaline waste solutions remains inadequately explored. We engineered the phoK gene (encoding a novel alkaline phosphatase, PhoK) from Sphingomonas sp. for overexpression in the radioresistant bacterium Deinococcus radiodurans. The recombinant strain thus obtained (Deino-PhoK) exhibited remarkably high alkaline phosphatase activity as evidenced by zymographic and enzyme activity assays. Deino-PhoK cells could efficiently precipitate uranium over a wide range of input U concentrations. At low uranyl concentrations (1 mM), the strain precipitated >90% of uranium within 2 h while a high loading capacity of around 10.7 g U/g of dry weight of cells was achieved at 10 mM U concentration. Uranium bioprecipitation by Deino-PhoK cells was not affected in the presence of Cs and Sr, commonly present in intermediate and low level liquid radioactive waste, or after exposure to very high doses of ionizing radiation. Transmission electron micrographs revealed the extracellular nature of bioprecipitated U, while X-ray diffraction and fluorescence analysis identified the precipitated uranyl phosphate species as chernikovite. When immobilized into calcium alginate beads, Deino-PhoK cells efficiently removed uranium, which remained trapped in beads, thus accomplishing physical separation of precipitated uranyl phosphate from solutions. The data demonstrate superior ability of Deino-PhoK, over earlier reported strains, in removal of uranium from alkaline solutions and its potential use in

  18. Bioprecipitation of uranium from alkaline waste solutions using recombinant Deinococcus radiodurans

    Energy Technology Data Exchange (ETDEWEB)

    Kulkarni, Sayali; Ballal, Anand; Apte, Shree Kumar, E-mail: aptesk@barc.gov.in

    2013-11-15

    Highlights: • Deinococcus radiodurans was genetically engineered to overexpress alkaline phosphatase (PhoK). • Deino-PhoK bioprecipitated U efficiently over a wide range of input U concentration. • A maximal loading of 10.7 g U/g of biomass at 10 mM input U was observed. • Radioresistance and U precipitation by Deino-PhoK remained unaffected by γ radiation. • Immobilization of Deino-PhoK facilitated easy separation of precipitated U. -- Abstract: Bioremediation of uranium (U) from alkaline waste solutions remains inadequately explored. We engineered the phoK gene (encoding a novel alkaline phosphatase, PhoK) from Sphingomonas sp. for overexpression in the radioresistant bacterium Deinococcus radiodurans. The recombinant strain thus obtained (Deino-PhoK) exhibited remarkably high alkaline phosphatase activity as evidenced by zymographic and enzyme activity assays. Deino-PhoK cells could efficiently precipitate uranium over a wide range of input U concentrations. At low uranyl concentrations (1 mM), the strain precipitated >90% of uranium within 2 h while a high loading capacity of around 10.7 g U/g of dry weight of cells was achieved at 10 mM U concentration. Uranium bioprecipitation by Deino-PhoK cells was not affected in the presence of Cs and Sr, commonly present in intermediate and low level liquid radioactive waste, or after exposure to very high doses of ionizing radiation. Transmission electron micrographs revealed the extracellular nature of bioprecipitated U, while X-ray diffraction and fluorescence analysis identified the precipitated uranyl phosphate species as chernikovite. When immobilized into calcium alginate beads, Deino-PhoK cells efficiently removed uranium, which remained trapped in beads, thus accomplishing physical separation of precipitated uranyl phosphate from solutions. The data demonstrate superior ability of Deino-PhoK, over earlier reported strains, in removal of uranium from alkaline solutions and its potential use in

  19. Particularities of anodic dissolution of rhenium in neutral and alkaline solutions at high current densities

    International Nuclear Information System (INIS)

    A study has been made of anodic dissolution of rhenium using potentiodynamic dissolution curves for a rotating disk electrode made of vacuum-melted rhenium. Dissolution of rhenium at 23 deg starts at potentials of approximately + 0.2 V for alkaline solutions (NaOH) and at potentials of approximately +0.1 V for neutral solutions (2N NaCl and NaNO3). No limitation of the process rate is observed during dissolution in neutral solutions unlike dissolution in alkalies for which a limiting current strength is characteristic

  20. Problems of evaluating isotope analysis of concentrated salt solutions in potash mines

    International Nuclear Information System (INIS)

    Three problems of quantitative evaluation of analytic D and 18O isotope data of concentrated salt solutions are discussed: (1) Consideration of the influence of admixtures of hydrated salts in determining meteoric or marine water fractions in a concentrated salt solution, (2) analytic accuracy and detection limits in determining meteoric water in salt solutions, and (3) processes of isotopic exchange with reservoir rock and sample matrix

  1. Temperature dependence of the absorbance of alkaline solutions of 4-nitrophenyl phosphate--a potential source of error in the measurement of alkaline phosphatase activity.

    Science.gov (United States)

    Burtis, C A; Seibert, L E; Baird, M A; Sampson, E J

    1977-09-01

    The absorbance of an alkaline solution of 4-nitrophenyl phosphate is a function of temperature. Quantitative evaluation of this phenomenon indicates that it (a) depends on the concentration of the compound and is independent of source, buffer concentration, and pH above 9.0; (b) is reversible; (c) is not a result of alkaline hydrolysis or 4-nitrophenol contamination; and (d) correlates with a temperature-induced shift of its absorbance spectrum. The phenomenon may represent a potential analytical problem in methods for alkaline phosphatase in which this compound is the substrate. If thermal equilibrium is not reached and maintained during an alkaline phosphatase assay, the thermochromic response will be included in the measured rate. The magnitude of this error depends on the thermal response and control characteristics of each particular instrument and the reaction conditions under which such an analysis is performed. PMID:19164

  2. Chemical perspectives on alkali and earth alkaline nitrate and nitrite salts for concentrated solar power applications

    Energy Technology Data Exchange (ETDEWEB)

    Cordaro, Joseph G. [Sandia National Labsoratories, Livermore, CA (United States)

    2013-04-01

    Molten salts have been widely considered as the leading candidate heat transfer fluids (HTF) used in high temperature, concentrated solar power plants. Specifically, nitrate and nitrite based salts have been investigated as a HTF and even deployed in pilot plants generating up to 19.9 MW of electricity at operating temperatures above 500 C. New plant designs requiring higher operating temperatures for better efficiencies are pushing the stability limit of HTF. This paper presents an overview of the thermophysical properties of nitrate and nitrite salts and discusses thermodynamic and kinetic stability limitations as they relate to concentrated solar power generation. (orig.)

  3. Blending Of Radioactive Salt Solutions In Million Gallon Tanks

    Energy Technology Data Exchange (ETDEWEB)

    Leishear, Robert A.; Lee, Si Y.; Fowley, Mark D.; Poirier, Michael R.

    2012-12-10

    Research was completed at Savannah River National Laboratory (SRNL) to investigate processes related to the blending of radioactive, liquid waste, salt solutions in 4920 cubic meter, 25.9 meter diameter storage tanks. One process was the blending of large salt solution batches (up to 1135 ? 3028 cubic meters), using submerged centrifugal pumps. A second process was the disturbance of a settled layer of solids, or sludge, on the tank bottom. And a third investigated process was the settling rate of sludge solids if suspended into slurries by the blending pump. To investigate these processes, experiments, CFD models (computational fluid dynamics), and theory were applied. Experiments were performed using simulated, non-radioactive, salt solutions referred to as supernates, and a layer of settled solids referred to as sludge. Blending experiments were performed in a 2.44 meter diameter pilot scale tank, and flow rate measurements and settling tests were performed at both pilot scale and full scale. A summary of the research is presented here to demonstrate the adage that, ?One good experiment fixes a lot of good theory?. Experimental testing was required to benchmark CFD models, or the models would have been incorrectly used. In fact, CFD safety factors were established by this research to predict full-scale blending performance. CFD models were used to determine pump design requirements, predict blending times, and cut costs several million dollars by reducing the number of required blending pumps. This research contributed to DOE missions to permanently close the remaining 47 of 51 SRS waste storage tanks.

  4. Electromigration behavior of SSDNA fragments in highly alkaline solutions of linear polyacrylamide

    Czech Academy of Sciences Publication Activity Database

    Malá, Zdeňka; Klepárník, Karel; Boček, Petr

    Boston: CaSSS, 2001, s. 156. [HPCE 2001. International Symposium on Microscale Separations and Analysis Includes mini-symposia on Genomics and Proteomics /14./. Boston (US), 13.01.2001-18.01.2001] R&D Projects: GA ČR GA203/00/0772; GA ČR GA303/00/0928 Institutional research plan: CEZ:AV0Z4031919 Keywords : DNA sequencing * bare capillary * alkaline solution Subject RIV: CB - Analytical Chemistry, Separation

  5. Electrochemical Reduction of Oxygen on Multi-walled Carbon Nanotubes Electrode in Alkaline Solution

    Institute of Scientific and Technical Information of China (English)

    You Qun CHU; Chun An MA; Feng Ming ZHAO; Hui HUANG

    2004-01-01

    The multi-walled carbon nanotubes (MWNTs) electrode was constructed using poly- tetrafluoroethylene as binder, and the electrochemical reductive behavior of oxygen in alkaline solution was first examined on this electrode. Compared with other carbon materials, MWNTs show higher electrocatalytic activity, and the reversibility of O2 reduction reaction is greatly improved. The experiments reveal that the electrochemical reduction of O2 to HO2- is controlled by adsorption. The preliminary results illustrate the potential application of MWNTs in fuel cells.

  6. Electrochemical Characterization of New Silver Gas Diffusion Electrodes during Oxygen Reduction in Alkaline Solution

    OpenAIRE

    Wagner, Norbert

    2013-01-01

    In order to analyze in detail the kinetics of the oxygen reduction reaction (ORR) and the influence of the porous electrode structure on the electrode performance in alkaline solution (10 M NaOH) at 80°C electrochemical impedance measurements (EIS) and cyclic voltammograms (CV) have been performed. The investigated electrodes were technical silver gas diffusion electrodes (GDE) and porous silver membranes with different pore radii ranging from 0.2 µm to 5 µm. Silver gas diffusion electrodes w...

  7. Decontamination of alkaline solution from technetium and other fission products and from some actinides by reductive coprecipitation and sorption on metals

    Energy Technology Data Exchange (ETDEWEB)

    Peretrukhin, V.F.; Silin, V.I.; Tananaev, I.G.; Kareta, A.V.; Trushina, V.E. [Russian Academy of Sciences, Moscow (Russian Federation). Institute of Physical Chemistry

    1997-09-01

    Effective decontamination of alkaline solutions and Hanford Site tank waste simulants from technetium has been accomplished by reductive coprecipitation with iron(III) hydroxide. Addition of 1 M (NH{sub 4}){sub 2}Fe(SO{sub 4}){sub 2} to 0.5 to 4.0 M NaOH to a final concentration of 0.1 to 0.15 M coprecipitates more than 99% of the technetium. from 0.5 to 1.0 M NaOH and 98 to 96% from 2.0 to 4.0 M NaOH. Similar results were obtained by reduction of Tc(VII) with 0.1 to 0.15 M hydrazine and subsequent addition of FeCl{sub 3} to a final concentration of 0.15 M. Inclusion of four complex-forming agents [0.01 M phosphate, 0.1 M EDTA (ethylenediaminetetraacetate), 0.03 M citrate, and 0.1 M glycolate (HOCH{sub 2}CO{sub 2}{sup -})] to the alkaline solution decreases technetium coprecipitation with iron hydroxide to 85% under otherwise similar conditions. Inclusion of 0.04 M Na{sub 2}CrO{sub 4} drastically decreases reductive coprecipitation of Tc(VII) in 0.5 to 4.0 M NaOH. Iron(II) salt, added to a 0.07 M excess over that of chromate, completely reduces chromate and provides greater than 99% coprecipitation of technetium with product iron(III) and chromium(III) hydroxides. Technetium(VII) reduction by hydrazine is slow in the presence of chromate in alkaline solution, and technetium coprecipitation is incomplete in these conditions. Decontamination of an alkaline Hanford Site tank waste simulant, containing 0.04M chromate and eleven salts and complex-forming agents, by adding 1 M iron(II) salt solution was studied. Coprecipitation of 15 to 28% of the technetium and more than 99% of the plutonium occurred in the Fe/Cr(III) hydroxide precipitate produced by adding 0.05 to 0.10 M iron(II). Chromate reduction was incomplete. About 75% of the technetium was coprecipitated, and the chromate was completely reduced, after adding 0.2 M iron(II) salt.

  8. Experiences in the capture of combustion gases of rice husk with alkaline solutions

    OpenAIRE

    Abelardo Prada Matiz; Caroll Edith Cortés Castillo

    2011-01-01

    The present work is aimed at studying the processes of capture of combustion gases of rice husk with alkaline solutions of sodium hydroxide (NaOH) and potassium hydroxide (KOH) and its subsequent transformation into calcium carbonate (CaCO3), a substance useful in agriculture, by adding calcium chloride(CaCl2) in aqueous solution. Was determined the basic characteristics of the process of capture of combustion gases such as reaction time, pH, mass and performance of calcium carbonate (CaCO3) ...

  9. Thermochemical study of gaseous oxy salts. Communication 7. Alkaline earth metal niobates

    International Nuclear Information System (INIS)

    Existence of gaseous niobates of alkaline-earth metals was ascertained by the method of high-temperature mass-spectrometry. Equilibrium constants involving the molecules and the relevant oxides were calculated, the standard enthalpies of formation and atomization for gaseous BeNbO3, CaNbO3, SrNbO3, BaNbO2, BaNbO3 and BaNb2O6 were determined

  10. Interactions of N,N'-dimethylaminoethanol with steel surfaces in alkaline and chlorine containing solutions

    Science.gov (United States)

    Welle, A.; Liao, J. D.; Kaiser, K.; Grunze, M.; Mäder, U.; Blank, N.

    1997-10-01

    Formulations based on dilute aqueous solutions of N,N'-dimethylethanolamine (DMEA) are used to protect reinforcement steel bars ('rebar') in concrete from corrosion. In a previous paper we discussed the usefulness of X-ray photoelectron spectroscopy (XPS) to detect DMEA adsorbed from solution and the application of secondary neutral mass spectrometry (SNMS) to study migration of DMEA through a cement matrix. In this report we present XPS data of DMEA adsorbed on steel surfaces from alkaline and chlorine containing solutions of variable concentration range and discuss models for the interaction of DMEA with the oxidized steel surface and the mechanism of corrosion inhibition of DMEA. DMEA is strongly bonded to the steel surface and displaces ionic species from the substrate/solution interface hence protecting the ironoxide surface from ionic attack.

  11. Comparative study of polypyrrole films electrosynthesized in alkaline and acid solutions

    International Nuclear Information System (INIS)

    The influence of the pH of electropolymerization solutions on the properties of polypyrrole films has been studied using potentiodynamic techniques and faradaic impedance spectroscopy. Scanning electron microscopy (SEM), IR and Raman spectroscopies, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were also used for products characterization. Results indicate that, contrary to what happen with the polymer electrogenerated in acid solutions, the films prepared in alkaline media are stable and present good electrochemical activity in basic solutions. Possible explanations for the observed differences are discussed and it is proposed that the pH of electropolymerization medium directly affects chains organization. Electrosynthesis in solutions of increased basicity results in a more compact and closed polymer structure.

  12. Detection of salt bridges to lysines in solution in barnase

    DEFF Research Database (Denmark)

    Hansen, Poul Erik; Williamson, Michael P.; Hounslow, Andrea M.; Ford, Joe; Fowler, Kyle; Hebditch, Max

    2013-01-01

    We show that salt bridges involving lysines can be detected by deuterium isotope effects on NMR chemical shifts of the sidechain amine. Lys27 in the ribonuclease barnase is salt bridged, and mutation of Arg69 to Lys retains a partially buried salt bridge. The salt bridges are functionally important....

  13. Alleviating salt stress in tomato seedlings using Arthrobacter and Bacillus megaterium isolated from the rhizosphere of wild plants grown on saline-alkaline lands.

    Science.gov (United States)

    Fan, Pengfei; Chen, Daitao; He, Yanan; Zhou, Qingxia; Tian, Yongqiang; Gao, Lihong

    2016-11-01

    Salt-induced soil degradation is common in farmlands and limits the growth and development of numerous crop plants in the world. In this study, we isolated salt-tolerant bacteria from the rhizosphere of Tamarix chinensis, Suaeda salsa and Zoysia sinica, which are common wild plants grown on a saline-alkaline land, to test these bacteria's efficiency in alleviating salt stress in tomato plants. We screened out seven strains (TF1-7) that are efficient in reducing salt stress in tomato seedlings. The sequence data of 16S rRNA genes showed that these strains belong to Arthrobacter and Bacillus megaterium. All strains could hydrolyze casein and solubilize phosphate, and showed at least one plant growth promotion (PGP)-related gene, indicating their potential in promoting plant growth. The Arthrobacter strains TF1 and TF7 and the Bacillus megaterium strain TF2 and TF3 could produce indole acetic acid under salt stress, further demonstrating their PGP potential. Tomato seed germination, seedling length, vigor index, and plant fresh and dry weight were enhanced by inoculation of Arthrobacter and B. megaterium strains under salt stress. Our results demonstrated that salt-tolerant bacteria isolated from the rhizosphere of wild plants grown on saline-alkaline lands could be used for alleviating salt stress in crop plants. PMID:27196364

  14. Study of the electrochemical oxidation mechanism of formaldehyde on gold electrode in alkaline solution

    Institute of Scientific and Technical Information of China (English)

    Rui-Wen Yan; Bao-Kang Jin

    2013-01-01

    The oxidation of formaldehyde in alkaline solution was studied by in situ rapid-scan time-resolved IR spectroelectrochemistry (RS-TR-FTIRS) method.In the potential range between-0.7 V and 0.2 V,the gem-diol anions were oxidized (according to the 2765 cm-1 ofvH-o and 1034 cm-1 ofvco downward IR bands) and the formate ions appeared (according to the 1588,1357 cm-1 of the asymmetric and symmetricvoco and 1380 cm-1 ofδc-H upward IR bands) in aqueous solution.It was also confirmed that gem-diol anion was oxidized (according to the 2026,1034 cm-1 downward IR bands) to formate ions (according to the 1595,1357,1380 cm-1 upward IR bands) and water (according to the 3427 cm-1 ofvH-o upward IR band) in heavy water solution.The results illustrated that formaldehyde formed gem-diol anion in alkaline solution and was absorbed on the electrode surface; then gem-diol anion was oxidized to formate ions and water.

  15. Carbon footprint of geopolymeric mortar: Study of the contribution of the alkaline activating solution and assessment of an alternative route

    OpenAIRE

    Mellado Romero, Ana María; CATALAN, C; Bouzón, N.; Borrachero Rosado, María Victoria; Monzó Balbuena, José Mª; Paya Bernabeu, Jorge Juan

    2014-01-01

    CO2 emissions associated with geopolymeric mortar prepared using spent fluid catalytic cracking catalyst (FCC) were compared to those calculated for plain ordinary Portland cement (OPC) mortar. Commercial waterglass used for preparing the alkaline activating solution for geopolymeric mortar was the main contributing component related to CO2 emission. An alternative route for formulating alkaline activating solution in the preparation of the geopolymeric binder was proposed: refluxing of rice ...

  16. Collapse of sodium polyacrylate chains in calcium salt solutions

    Science.gov (United States)

    Schweins, R.; Huber, K.

    The sodium salt of polyacrylic acid (NaPA) precipitates in the presence of Ca^{2+}-ions. This phase behaviour can be represented by a phase diagram where the critical NaPA concentration is plotted versus the critical Ca^{2+} concentration resulting in a straight line as a phase boundary. The location of this phase boundary is influenced by the presence of an inert monovalent salt like NaCl. The present contribution focuses on the coil dimensions of NaPA chains in dilute aqueous solution corresponding to the one phase region of such a phase diagram. A variety of parameters with which the size and shape of the polyelectrolyte chains can be modulated are revealed. Approaching the phase boundary by decreasing the NaPA concentration at a constant Ca^{2+} content leads to a collapse of the NaPA chains. Combined static and dynamic light scattering suggests a compact spherical shape as the final state of this transition, both in 0.1 M NaCl and in 0.01 M NaCl. In the lower NaCl concentration, indication is presented for the existence of a cigar or pearl necklace like intermediate. Most strikingly, the collapsed chains can be reexpanded by increasing the concentration of inert NaCl at constant content of NaPA and Ca^{2+}. Clearly, excessive Na+-ions displace the Ca^{2+}-ions from the NaPA chains.

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

    International Nuclear Information System (INIS)

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

  18. Radiation-induced reduction of ditetrazolium salt in aqueous solutions

    International Nuclear Information System (INIS)

    Color formation in aqueous solutions of the ditetrazolium salt blue tetrazolium (BT2+) in the absence or presence of oxygen is a complex radiation chemical reaction. The final stable product is the poorly soluble diformazan violet to blue pigment having a broad spectral absorption band (λmax=552 nm). The reaction of BT2+ with the hydrated electron proceeds by rapid reduction of BT2+ followed by protonation at the nitrogen closest to the unsubstituted phenyl group, via the two intermediate tetrazolinyl radicals shared by the ditetrazole ring nitrogens. The effect of solution pH, N2O saturation, and the presence of the reducing agent dextrose are examined. The system serves as a radiochromic sensor and a dosimeter of ionizing radiations. Solutions of 5 mmol l-1 BT2+ at pH 7.3 serve as dosimeters over an absorbed-dose range of approximately 0.2-6 kGy (dearated, with a range of 1-8 mmol l-1 dextrose) and of about 1-15 kGy (aerated, with 0.1 mol l-1 sodium formate and 5 mmol l-1 dextrose)

  19. Bioreactor for the decolourisation of textile dye using ligninolytic fungi under high alkaline and salt conditions

    OpenAIRE

    Ottoni, C. A.; Lima, Luís; Santos, C.; Lima, Nelson

    2011-01-01

    The wastewater of textile industry contains not only dyes but also salts, surfactants and others substances and as extreme pH values. Among all dyes and pigments azo dyes are claimed to be between 60 to 70% of the environmental pollutants. Nowadays, environmental regulations in most countries require textile effluents to be decolourised before discharging. This led to the study of innovative and environmental friendly technologies. The extracellular ligninolytic enzyme system o...

  20. 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.

  1. Pitting corrosion of friction stir welded aluminum alloy thick plate in alkaline chloride solution

    Energy Technology Data Exchange (ETDEWEB)

    Xu Weifeng, E-mail: xwf1982@mail.nwpu.edu.c [School of Materials and Engineering, Northwestern Polytechnical University, Xi' an 710072 (China); Liu Jinhe; Zhu Hongqiang [School of Materials and Engineering, Northwestern Polytechnical University, Xi' an 710072 (China)

    2010-03-01

    The pitting corrosion of different positions (Top, Middle and Bottom) of weld nugget zone (WNZ) along thickness plate in friction stir welded 2219-O aluminum alloy in alkaline chloride solution was investigated by using open circuit potential, cyclic polarization, scanning electron microscopy and atomic force microscope. The results indicate that the material presents significant passivation, the top has highest corrosion potential, pitting potential and re-passivation potential compared with the bottom and base material. With the increase of traverse speed from 60 to 100 mm/min or rotary speed from 500 to 600 rpm, the corrosion resistance decreases.

  2. Kinetics of leaching of the aluminum hydroxide in bauxites by alkaline solutions at atmospheric pressure

    Science.gov (United States)

    Burtsev, A. V.; Lainer, Yu. A.; Gorichev, I. G.; Kipriyanov, N. A.; Izotov, A. D.

    2011-11-01

    The kinetics of leaching of the aluminum hydroxide from the gibbsite bauxites of Guinea (Kindia deposit) is studied under atmospheric conditions. The activation energy of the process is found to be 34.75 kJ/mol, which indicates that the process proceeds in a kinetic mode. The leaching of the aluminum hydroxide from bauxite in an alkaline solution is simulated using acid-base equilibria (ion exchange) and the electrochemical theory of the structure of a double electrical layer (Gram-Parsons theory).

  3. EIS ANALYSIS ON THE ANODIC PROCESS OF ZINC IN AN ALKALINE SOLUTION

    Institute of Scientific and Technical Information of China (English)

    Y. Zheng; J.M. Wang; H. Chen; J.Q. Zhang; C.N. Cao

    2004-01-01

    The EIS on the anodic process of pure Zn in an alkaline solution were performed and fitted using the expression of Faradic admittance, based on which the mechanism of the process was proposed. The results showed that besides electrode potential E the electrochemical reaction rate was affected by the adsorption of Zn(OH)ads on the electrode surface and the diffusion of in the electrolyte in active region, and only by the covering of passivation layer on the electrode surface in both transitive and passivation regions. The equivalent circuits applied in these various circumstances were proposed and the variation of some parameters and state variables was also discussed.

  4. Galvanic Corrosion between Alloy 690 and Magnetite in Alkaline Aqueous Solutions

    OpenAIRE

    Soon-Hyeok Jeon; Geun-Dong Song; Do Haeng Hur

    2015-01-01

    The galvanic corrosion behavior of Alloy 690 coupled with magnetite has been investigated in an alkaline solution at 30 °C and 60 °C using a potentiodynamic polarization method and a zero resistance ammeter. The positive current values were recorded in the galvanic couple and the corrosion potential of Alloy 690 was relatively lower. These results indicate that Alloy 690 behaves as the anode of the pair. The galvanic coupling between Alloy 690 and magnetite increased the corrosion rate of All...

  5. Pitting corrosion of friction stir welded aluminum alloy thick plate in alkaline chloride solution

    International Nuclear Information System (INIS)

    The pitting corrosion of different positions (Top, Middle and Bottom) of weld nugget zone (WNZ) along thickness plate in friction stir welded 2219-O aluminum alloy in alkaline chloride solution was investigated by using open circuit potential, cyclic polarization, scanning electron microscopy and atomic force microscope. The results indicate that the material presents significant passivation, the top has highest corrosion potential, pitting potential and re-passivation potential compared with the bottom and base material. With the increase of traverse speed from 60 to 100 mm/min or rotary speed from 500 to 600 rpm, the corrosion resistance decreases.

  6. Preparation, characterization and application of alkaline leached CuNiZn ternary coatings for long-term electrolysis in alkaline solution

    Energy Technology Data Exchange (ETDEWEB)

    Solmaz, Ramazan [Bingoel University, Science and Letters Faculty, Chemistry Department, 12000 Bingoel (Turkey); Doener, Ali; Kardas, Guelfeza [Cukurova University, Science and Letters Faculty, Chemistry Department, 01330 Balcali Adana (Turkey)

    2010-10-15

    The NiCuZn ternary coating was electrochemically deposited on a copper electrode. Then, it was etched in a concentrated alkaline solution (30% NaOH) to produce a porous and electrocatalytic surface suitable for use in the hydrogen evolution reaction (HER). The surface composition of coating before and after alkaline leaching was determined by energy dispersive X-ray (EDX) analysis. The surface morphologies were investigated by scanning electron microscopy (SEM). The long-term stability of electrode prepared for alkaline water electrolysis was investigated in 1 M KOH solution with the help of cathodic current-potential curves and electrochemical impedance spectroscopy (EIS) techniques. It was found that, the NiCuZn coating has a compact and porous structure with good physical stability. Alkaline leaching process further improved the activity of NiCuZn coating in comparison with binary NiCu deposit for the HER. The long-term operation at -100 mA cm{sup -2} showed good electrochemical stability over 120 h. (author)

  7. Alkaline deoxygenated graphene oxide as adsorbent for cadmium ions removal from aqueous solutions.

    Science.gov (United States)

    Liu, Jun; Du, Hongyan; Yuan, Shaowei; He, Wanxia; Yan, Pengju; Liu, Zhanhong

    2015-01-01

    Alkaline deoxygenated graphene oxide (aGO) was prepared through alkaline hydrothermal treatment and used as adsorbent to remove Cd(II) ions from aqueous solutions for the first time. The characterization results of transmission electron microscopy, X-ray diffraction, Raman spectroscopy, and Fourier transform infrared (FT-IR) spectra indicate that aGO was successfully synthesized. The batch adsorption experiments showed that the adsorption kinetics could be described by the pseudo-second-order kinetic model, and the isotherms equilibrium data were well fitted with the Langmuir model. The maximum adsorption capacity of Cd(II) on aGO was 156 mg/g at pH 5 and T=293 K. The adsorption thermodynamic parameters indicated that the adsorption process was a spontaneous and endothermic reaction. The mainly adsorption mechanism speculated from FT-IR results may be attributed to the electrostatic attraction between Cd2+ and negatively charged groups (-CO-) of aGO and cation-π interaction between Cd2+ and the graphene planes. The findings of this study demonstrate the potential utility of the nanomaterial aGO as an effective adsorbent for Cd(II) removal from aqueous solutions. PMID:26038925

  8. Mechanism of pitting corrosion prevention by nitrite in carbon steel exposed to dilute salt solutions. 1998 annual progress report

    International Nuclear Information System (INIS)

    'The overall goal of this project is to develop a fundamental understanding of the role of nitrite in preventing the breakdown of protective oxide(s) on carbon steel and the onset of pitting. Pitting corrosion of carbon steel exposed to dilute alkaline salt solutions can be induced by nitrate, sulfate, and chloride ions and is prevented by sufficient concentration of nitrite. A significant example of this material/electrolyte system is the storage and processing of DOE''s high-level radioactive liquid waste in carbon steel tanks. Added nitrite in the waste has a considerable downstream impact on the immobilization of the waste in a stable glass form. Waste tank integrity and glass production efficiency may benefit from the fundamental understanding of nitrite''s role in preventing pitting. This report summarizes progress after approximately six months of effort in this three-year EMSP project. Initial experimental and theoretical work has focused on the electrochemical behavior of carbon steel in simplified non-radioactive solutions that simulate complex dilute radioactive waste solutions. These solutions contain corrosion-inducing species such as nitrate and chloride and the corrosion-inhibiting nitrite at moderately alkaline pHs. The electrochemical behavior of interest here is that of the open-circuit potential of the steel specimen at equilibrium in the experimental electrolyte and the measures of the steel''s passivity and passivity breakdown.'

  9. Electrodeposition of actinide traces from aqueous alkaline solutions and tributyl phosphate

    International Nuclear Information System (INIS)

    The electrodeposition of uranium and trace quantities of 239Pu, 234Th, 144Ce on a stainless steel disk was investigated from 0.5-2.0M NaOH and the two-phase system, extract of actinides in TBP-aqueous solution of NaOH. The electrodeposition yield of the above elements reaches 98-100% in 40 min of electrolysis with current density 0.4-0.5 A/cm2. The presence of 0.5M Na2CO3, 2.0M NaNO3, 2.0M NaNO2, 0.2M NaF in alkaline solutions does not decrease the electrodeposition yield. The electrodeposited films meet all the requirements of α-spectrometry. The uranium oxidation states (V) and (IV) were determined in the electrodeposited films. (author) 9 refs.; 3 figs.; 1 tab

  10. Reaction of montmorillonite in alkaline solution at 60 C, 90 C, 120 C and 180 C

    International Nuclear Information System (INIS)

    The reaction of montmorillonite was investigated. Three kinds of bentonites with different montmorillonite composition were mixed with 0.3M NaOH solution and 0.3M Ca(OH)2 slurry. They were immersed at 60 C, 90 C, 120 C, and 180 C for one month, three months and six months. The concentrations of the soluble ions were measured and the bentonites were analyzed quantitatively after the immersion. 50% of the montmorillonite was reacted within two weeks at greater than 90 C. Montmorillonite reacts less when mixed with Si-minerals. It extensively reacted in 0.3M Ca(OH)2 slurry. These results suggest that the reaction mechanism of the montmorillonite in alkaline solution was dominantly Si dissolution, and would decrease by controlling the concentration of Si ion. The cement/bentonite system under Si saturated conditions is discussed

  11. On the complex structural diffusion of proton holes in nanoconfined alkaline solutions within slit pores.

    Science.gov (United States)

    Muñoz-Santiburcio, Daniel; Marx, Dominik

    2016-01-01

    The hydroxide anion OH(-)(aq) in homogeneous bulk water, that is, the solvated proton hole, is known to feature peculiar properties compared with excess protons solvated therein. In this work, it is disclosed that nanoconfinement of such alkaline aqueous solutions strongly affects the key structural and dynamical properties of OH(-)(aq) compared with the bulk limit. The combined effect of the preferred hypercoordinated solvation pattern of OH(-)(aq), its preferred perpendicular orientation relative to the confining surfaces, the pronounced layering of nanoconfined water and the topology of the hydrogen bond network required for proton hole transfer lead to major changes of the charge transport mechanism, in such a way that the proton hole migration mechanism depends exquisitely on the width of the confined space that hosts the water film. Moreover, the anionic Zundel complex, which is of transient nature in homogeneous bulk solutions, can be dynamically trapped as a shallow intermediate species by suitable nanoconfinement conditions. PMID:27550616

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

    International Nuclear Information System (INIS)

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

  13. Investigation of electrochemical synthesis of ferrate, Part I: Electrochemical behavior of iron and its several alloys in concentrated alkaline solutions

    Directory of Open Access Journals (Sweden)

    Čekerevac Milan I.

    2009-01-01

    Full Text Available In recent years, considerable attention has been paid to various applications of Fe(VI due to its unique properties such as oxidizing power, selective reactivity, stability of the salt, and non-toxic decomposition by-products of ferric ion. In environmental remediation processes, Fe(VI has been proposed as green oxidant, coagulant, disinfectant, and antifoulant. Therefore, it is considered as a promising multi-purpose water treatment chemical. Fe(VI has also potential applications in electrochemical energy source, as 'green cathode'. The effectiveness of ferrate as a powerful oxidant in the entire pH range, and its use in environmental applications for the removal of wide range of contaminants has been well documented by several researchers. There is scientific evidence that ferrate can effectively remove arsenic, algae, viruses, pharmaceutical waste, and other toxic heavy metals. Although Fe(VI was first discovered in early eighteen century, detailed studies on physical and chemical properties of Fe(VI had to wait until efficient synthetic and analytical methods of Fe(VI were developed by Schreyer et al. in the 1950s. Actually, there have been developed three ways for the preparation of Fe(VI compounds : the wet oxidation of Fe(II and Fe(III compounds, the dry oxidation of the same, and the electrochemistry method, mainly based on the trans passive oxidation of iron. High purity ferrates Fe(VI can be generated when electrode of the pure iron metal or its alloys are anodized in concentrated alkaline solution. It is known that the efficiency of electrochemical process of Fe(VI production depends on many factors such as current density, composition of anode material, types of electrolyte etc. In this paper, the electrochemical synthesis of ferrate(VI solution by the anodic dissolution of iron and its alloys in concentrated water solution of NaOH and KOH is investigated. The process of transpassive dissolution of iron to ferrate(VI was studied by

  14. The influence of temperature and inorganic salts on therheological properties of xanthan aqueous solutions

    OpenAIRE

    KATARINA JEREMIC; SINISA MARKOV; BRANISLAV PEKIC; SLOBODAN JOVANOVIC; MIRJANA S. PAVLOVIC

    1999-01-01

    The rheological properties of xanthan gum in aqueous saline solutions and at increased temperatures are of great practical interest especially for its application in enhanced oil recovery during which the xanthan solutions are exposed to increased salt contents and relatively high temperatures. In this work, the influence of high temperature and high salt concentrations (up to 10 mass%) on the rheological properties of xanthan was investigated. The influence of three different salts was exami...

  15. Alkaline leaching of metal melting industry wastes dseparation of zinc and lead in the leach solution

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    In this work, a thorough examinations on the extractability of zinc and lead present in the steelmaking dusts using alkaline leaching process and the effectiveness of the zinc and lead separation in the resultant leaching solutions using sulfide precipitation method were made. It was found that only about 53% of zinc and over 70% of the lead could be leached out of the dusts, while the other 47% of zinc and 306 of lead were left in the leaching residues. The zinc and lead in the resultant leaching solution can be effectively and selectively separated. When the weight ratio of sodium sulfide (M. W. = 222-240) to Pb was kept at 1.8, the lead in the solution could be precipitated out quantitatively while all the zinc was remained in the solution. The zinc left in the solution can be further recovered by the addition of extra sodium sulfide with a weight ratio of sodium sulfide to the zinc over 2.6. The resultant filtrate can be recycled to the leaching of dust in the next leaching process.

  16. Anodic treatment of strengthening the electrochemical coatings in electrolytes for electrochemical machining: 1. Micromachining of CoW coatings in nitrate and nitrate-alkaline solutions

    International Nuclear Information System (INIS)

    Polycrystalline CoW coatings (with a 5-6 at % content of W) were found to dissolve in a 2M NaNO3 solution with 100% current efficiency while reaching the conditions of thermo kinetic instability (TKI) upon attaining the anode limiting currents resulting from the salt's passivation. The anodic micromachining of nanocrystalline coatings (22-25 at % of W) in a nitrate solution also occurs with a 100% current efficiency, though at a very high degree of dissolution instability prior to attaining the TKI. The electrochemical micromachining of nanocrystalline coatings in a nitrate-alkaline solution (2M NaNO2 + 0.5 M KOH) at low current densities occurs at a current efficiency close to zero, but, in all the cases under the TKI conditions, the current efficiency (upon the coatings treatment with different W contents in different solutions)exceeds the 100% value. A procedure for the removal of the coating material under the TKI conditions is offered that suggests the formation of an oxide-salt film and its periodic destruction due to a thermal explosion. It is shown that the minimal surface roughness is registered after the coating dissolution under the TKI conditions. Results are reported that confirm the possibility of controlling the strengthening (weakening) process of a surface layer after micromachining in different electrolytes using constant and pulse currents. (authors)

  17. Effect of salt solutions on chain structure of partially hydrolyzed polyacrylamide

    Institute of Scientific and Technical Information of China (English)

    张青; 周吉生; 翟永爱; 刘凤岐; 高歌

    2008-01-01

    The effect of salt solutions(NaCl,Na2SO4 and CaCl2) on the conformational properties of partially hydrolyzed polyacrylamide(HPAM) was investigated by using static laser light scattering(SLLS).The special interaction between CaCl2 solution and HPAM was also researched.Experimental results show that the chain structure of HPAM is interrelated with the charge density,the kind and the concentration of salt solutions.The mean-square radius of gyration(Rz) and the second virial coefficient(A2) of HPAM decrease with increasing concentration of salt solutions,and the salt effect tends towards the maximum when the concentration of salt solution is increased to some amount.

  18. Compositions for preparation of aqueous solutions of salts of lower valence /sup 99/Tc

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt-Dunker, M.; Greb, W.

    1979-01-09

    Aqueous solutions of /sup 99/Tc salts in which the /sup 99/Tc is in reduced valencey state, when administered to mammals, permit identification of the skeleton and of calcareous tumors by scintigraphy (radiographic scanning). The solutions are conveniently prepared by mixing one or more phosphonic acids (or their salts) with one or more reducing salts, and adding the mixture to an aqueous solution of a pharmaceutically acceptable /sup 99/pertechnetate salt. Reduction of the valence of the technetium occurs rapidly, and the resulting solution is adequately stable for use in scintigraphy. The phosphonic acid and reducing salt components can be premixed. Aqueous solutions of the premix are stable for long periods of time in the absence of free oxygen and the premix is stable to air so long as it is dry.

  19. Arsenophilic Bacterial Processes in Searles Lake: A Salt-saturated, Arsenic-rich, Alkaline Soda Lake.

    Science.gov (United States)

    Oremland, R. S.; Kulp, T. R.; Hoeft, S. E.; Miller, L. G.; Swizer Blum, J.; Stolz, J. F.

    2005-12-01

    Searles Lake, located in the Mojave Desert of California, is essentially a chemically-similar, concentrated version of Mono Lake, but having a much higher salinity (e.g., 340 vs. 90 g/L) and a greater dissolved inorganic arsenic content in its brine (e.g., 3.9 vs. 0.2 mM). The source of all this arsenic ultimately comes from hydrothermal spring inputs, thereby underscoring the importance of volcanic and fluvial processes in transporting this toxic element into these closed basin lakes. Nonetheless, the presence of microbial activities with regard to respiration of arsenate oxyanions under anaerobic conditions and the oxidation of arsenite oxyanions under aerobic conditions can be inferred from porewater profiles taken from handcores retrieved beneath Searles Lake's salt crust. Sediment slurry incubations confirmed biological arsenate respiration and arsenite oxidation, with the former processes notably enhanced by provision of the inorganic electron donor sulfide or H2. Hence, arsenic-linked chemo-autotrophy appears to be an important means of carbon fixation in this system. Subsequent efforts using 73As-arsenate as radiotracer detected dissimilatory arsenate reduction activity down the length of the core, but we were unable to detect any evidence for sulfate-reduction using 35S-sulfate. An extremely halophilic anaerobic bacterium of the order Haloanaerobiales [strain SLAS-1] was isolated from the sediments that grew via arsenate respiration using lactate or sulfide as its electron donors. These results show that, unlike sulfate-reduction, arsenic metabolism (i.e., both oxidation of arsenite and dissimilatory reduction of arsenate) is operative and even vigorous under the extreme conditions of salt-saturation and high pH. The occurrence of arsenophilic microbial processes in Searles Lake is relevant to the search for extant or extinct microbial life on Mars. It is evident from surface imagery that Mars had past episodes of volcanism, fluvial transport, and most

  20. Ternary diffusion of carbon dioxide in alkaline solutions of aqueous sodium hydroxide and aqueous sodium carbonate

    Energy Technology Data Exchange (ETDEWEB)

    Leaist, D.G.

    1985-07-01

    Carbon dioxide dissolved in alkaline solutions diffuses as bicarbonate and carbonate ions produced by the reactions CO/sub 2/+OH/sup -/=HCO/sub 3//sup -/ and CO/sub 2/+2OH/sup -/=CO/sub 3//sup 2 -/+H/sub 2/O. Ternary diffusion coefficients of the systems NaHCO/sub 3/+Na/sub 2/CO/sub 3/+H/sub 2/O and Na/sub 2/CO/sub 3/+NaOH+H/sub 2/O have been measured by a conductimetric technique at 298.15 K. The mixed electrolyte data are transformed by use of the solution equilibria to ternary diffusion coefficients of the systems CO/sub 2/+Na/sub 2/CO/sub 3/+H/sub 2/O and CO/sub 2/+NaOH+H/sub 2/O. Unlike the binary diffusivity of CO/sub 2/ in water (1.9 . 10/sup -9/ m/sup 2/ s/sup -1/), the ternary diffusivity of CO/sub 2/ in alkaline solutions is sensitive to concentration and varies from 0.9 . 10/sup -9/ to 3.5 . 10/sup -9/ m/sup 2/ s/sup -1/ at 298.15 K. Expressions are derived to estimate the transport coefficients of the components from the concentrations and diffusion coefficients of the constituent ions. At high pH values hydroxide-coupled transport leads to rapid diffusion of CO/sub 2/ as CO/sub 3//sup 2 -/. The results are consistent with the Onsager reciprocal relation for isothermal ternary diffusion.

  1. Density, viscosity, and N2O solubility of aqueous amino acid salt and amine amino acid salt solutions

    International Nuclear Information System (INIS)

    Highlights: ► Density of amino acid salt and amine amino acid salt. ► Viscosity of amino acid salt and amine amino acid salt. ► Henry’s law constant/N2O solubility of amino acid salt and amine amino acid salt. ► Schumpe model. Correlations for density, viscosity, and N2O solubility. - Abstract: Physicochemical properties of aqueous amino acid salt (AAS), potassium salt of sarcosine (KSAR) and aqueous amine amino acid salt (AAAS), 3-(methylamino)propylamine/sarcosine (SARMAPA) have been studied. Densities of KSAR were measured for sarcosine mole fraction 0.02 to 0.25 for temperature range 298.15 K to 353.15 K, the viscosities were measured for 0.02 to 0.10 mole fraction sarcosine (293.15 K to 343.15 K) while the N2O solubilities were measured from 0.02 to 0.10 mole fraction sarcosine solutions (298.15 K to 363.15 K). Densities of SARMAPA were measured for sarcosine mole fraction 0.02 to 0.23 for temperature range (298.15 K to 353.15 K), viscosities were measured for 0.02 to 0.16 mole fraction sarcosine (293.15 K to 343.15 K) while the N2O solubilities were measured from 0.02 to 0.16 mole fraction sarcosine solutions (298.15 K to 343.15 K). Experimental results were correlated well with empirical correlations and N2O solubility results for KSAR were predicted adequately by a Schumpe model. The solubilities of N2O in AAS and AAAS are significantly lower than values for amines. The solubilities vary as: amine > AAAS > AAS.

  2. Influence of Salts on Electrospinning of Aqueous and Nonaqueous Polymer Solutions

    Directory of Open Access Journals (Sweden)

    Fatma Yalcinkaya

    2015-01-01

    Full Text Available A roller electrospinning system was used to produce nanofibres by using different solution systems. Although the process of electrospinning has been known for over half a century, knowledge about spinning behaviour is still lacking. In this work, we investigated the effects of salt for two solution systems on spinning performance, fibre diameter, and web structure. Polyurethane (PU and polyethylene oxide (PEO were used as polymer, and tetraethylammonium bromide and lithium chloride were used as salt. Both polymer and salt concentrations had a noteworthy influence on the spinning performance, morphology, and diameter of the nanofibres. Results indicated that adding salt increased the spinnability of PU. Salt created complex bonding with dimethylformamide solvent and PU polymer. Salt added to PEO solution decreased the spinning performance of fibres while creating thin nanofibres, as explained by the leaky dielectric model.

  3. XANES Demonstrates the Release of Calcium Phosphates from Alkaline Vertisols to Moderately Acidified Solution.

    Science.gov (United States)

    Andersson, Karl O; Tighe, Matthew K; Guppy, Christopher N; Milham, Paul J; McLaren, Timothy I; Schefe, Cassandra R; Lombi, Enzo

    2016-04-19

    Calcium phosphate (CaP) minerals may comprise the main phosphorus (P) reserve in alkaline soils, with solubility dependent on pH and the concentration of Ca and/or P in solution. Combining several techniques in a novel way, we studied these phenomena by progressively depleting P from suspensions of two soils (low P) using an anion-exchange membrane (AEM) and from a third soil (high P) with AEM together with a cation-exchange membrane. Depletions commenced on untreated soil, then continued as pH was manipulated and maintained at three constant pH levels: the initial pH (pHi) and pH 6.5 and 5.5. Bulk P K-edge X-ray absorption near-edge structure (XANES) spectroscopy revealed that the main forms of inorganic P in each soil were apatite, a second more soluble CaP mineral, and smectite-sorbed P. With moderate depletion of P at pHi or pH 6.5, CaP minerals became more prominent in the spectra compared to sorbed species. The more soluble CaP minerals were depleted at pH 6.5, and all CaP minerals were exhausted at pH 5.5, showing that the CaP species present in these alkaline soils are soluble with decreases of pH in the range achievable by rhizosphere acidification. PMID:26974327

  4. Surface effect on the electronic and the magnetic properties of rock-salt alkaline-earth metal silicides

    International Nuclear Information System (INIS)

    An all electron ab-initio method was employed to study the electronic and the magnetic properties of the (001) surface of alkaline-earth metal silicides, CaSi, SrSi, and BaSi, in the rock-salt structure. The three compounds retain their ferromagnetic metallic properties at the surface. Due to the surface effects, the magnetism of the topmost layer is changed as compared with the bulk. This is a short-range effect. In CaSi, the magnetism of the surface layer is noticeably reduced, as compared with the bulk: magnetic moments (MMs) on both Ca and Si atoms are reduced. In SrSi (001), the polarization of electrons in the surface atoms is similar to that in the bulk atoms, and the values of MMs on the component atoms in the topmost layer do not change as much as in CaSi. In BaSi (001), the magnetic properties of Si surface atoms are enhanced slightly, and the magnetism of Ba atoms is not affected considerably by the surface effect. The calculated densities of states confirm the short-range effect of the surface on the electronic properties of the metal silicides.

  5. ISOPAR L RELEASE RATES FROM SALTSTONE USING SIMULATED SALT SOLUTIONS

    Energy Technology Data Exchange (ETDEWEB)

    Zamecnik, J; Michael Bronikowski, M; Alex Cozzi, A; Russell Eibling, R; Charles Nash, C

    2008-07-31

    The Modular Caustic-Side Solvent Extraction (CSSX) Unit (MCU) and the Salt Waste Processing Facility (SWPF) will produce a Decontaminated Salt Solution (DSS) that will go to the Saltstone Production Facility (SPF). Recent information indicates that solvent entrainment in the DSS is larger than expected. The main concern is with Isopar{reg_sign} L, the diluent in the solvent mixture, and its flammability in the saltstone vault. If it is assumed that all the Isopar{reg_sign} L is released instantaneously into the vault from the curing grout before each subsequent pour, the Isopar{reg_sign} L in the vault headspace is well mixed, and each pour displaces an equivalent volume of headspace, the maximum concentration of Isopar{reg_sign} L in the DSS to assure 25% of the lower flammable limit is not exceeded has been determined to be about 4 ppm. The amount allowed would be higher if the release from grout were significantly less. The Savannah River National Laboratory was tasked with determining the release of Isopar{reg_sign} L from saltstone prepared with a simulated DSS with Isopar{reg_sign} L concentrations ranging from 50 to 200 mg/L in the salt fraction and with test temperatures ranging from ambient to 95 C. The results from the curing of the saltstone showed that the amount of Isopar{reg_sign} L released versus time can be treated as a percentage of initial amount present; there was no statistically significant dependence of the release rate on the initial concentration. The majority of the Isopar{reg_sign} L that was released over the test duration was released in the first few days. The release of Isopar{reg_sign} L begins immediately and the rate of release decreases over time. At higher temperatures the immediate release rate is larger than at lower temperatures. Initial curing temperature was found to be very important as slight variations during the first few hours or days had a significant effect on the amount of Isopar{reg_sign} L released. Short scoping

  6. ISOPAR L Release Rates from Saltstone Using Simulated Salt Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Bronikowski, M

    2006-02-06

    The Modular Caustic-Side Solvent Extraction (CSSX) Unit (MCU) and the Salt Waste Processing Facility (SWPF) will produce a Deactivated Salt Solution (DSS) that will go to the Saltstone Production Facility (SPF). Recent information indicates that solvent entrainment in the DSS is larger than expected. The main concern is with Isopar{reg_sign} L, the diluent in the solvent mixture, and its flammability in the saltstone vault. If it is assumed that all the Isopar{reg_sign} L is released instantaneously into the vault from the curing grout before each subsequent pour; the Isopar{reg_sign} L in the vault headspace is well mixed; and each pour displaces an equivalent volume of headspace, the allowable concentration of Isopar{reg_sign} L in the DSS sent to SPF has been calculated at approximately 4 ppm. The amount allowed would be higher, if the release from grout were significantly less. The Savannah River National Laboratory was tasked with determining the release of Isopar{reg_sign} L from saltstone prepared with a simulated DSS with Isopar{reg_sign} L concentrations ranging from 50 mg/L to 200 mg/L in the salt fraction and with test temperatures ranging from ambient to 95 C. The results from the curing of the saltstone showed that the Isopar{reg_sign} L release data can be treated as a percentage of initial concentration in the concentration range studied. The majority of the Isopar{reg_sign} L that was released over the test duration was released in the first few days. The release of Isopar{reg_sign} L begins immediately and the rate of release decreases over time. At higher temperatures the immediate release is larger than at lower temperatures. In one test at 95 C essentially all of the Isopar{reg_sign} L was released in three months. Initial curing temperature was found to be very important as slight variations during the first few days affected the final Isopar{reg_sign} L amount released. Short scoping tests at 95 C with solvent containing all components (Isopar

  7. Isopar L Release Rates from Saltstone Using Simulated Salt Solutions

    International Nuclear Information System (INIS)

    The Modular Caustic-Side Solvent Extraction (CSSX) Unit (MCU) and the Salt Waste Processing Facility (SWPF) will produce a Deactivated Salt Solution (DSS) that will go to the Saltstone Production Facility (SPF). Recent information indicates that solvent entrainment in the DSS is larger than expected. The main concern is with Isopar(regsign) L, the diluent in the solvent mixture, and its flammability in the saltstone vault. If it is assumed that all the Isopar(regsign) L is released instantaneously into the vault from the curing grout before each subsequent pour; the Isopar(regsign) L in the vault headspace is well mixed; and each pour displaces an equivalent volume of headspace, the allowable concentration of Isopar(regsign) L in the DSS sent to SPF has been calculated at approximately 4 ppm. The amount allowed would be higher, if the release from grout were significantly less. The Savannah River National Laboratory was tasked with determining the release of Isopar(regsign) L from saltstone prepared with a simulated DSS with Isopar(regsign) L concentrations ranging from 50 mg/L to 200 mg/L in the salt fraction and with test temperatures ranging from ambient to 95 C. The results from the curing of the saltstone showed that the Isopar(regsign) L release data can be treated as a percentage of initial concentration in the concentration range studied. The majority of the Isopar(regsign) L that was released over the test duration was released in the first few days. The release of Isopar(regsign) L begins immediately and the rate of release decreases over time. At higher temperatures the immediate release is larger than at lower temperatures. In one test at 95 C essentially all of the Isopar(regsign) L was released in three months. Initial curing temperature was found to be very important as slight variations during the first few days affected the final Isopar(regsign) L amount released. Short scoping tests at 95 C with solvent containing all components (Isopar(regsign) L

  8. CRIEPI's research results (2006-2011) and clarified future issues on alteration behavior of bentonite barrier by alkaline solutions

    International Nuclear Information System (INIS)

    In radioactive waste disposal facilities, bentonite barrier would be altered by alkaline solutions which arise by leaching of cementitious materials. Consequently suitable properties of the bentonite barrier would be degraded for a long time period. In CRIEPI, the investigation on the alteration of the bentonite under alkaline conditions was started in 2006, and several CRIEPI reports have been published. Specifically, we have investigated the kinetics of montmorillonite dissolution, the mineralogical alteration of compacted bentonite (with high- and low-dry density) and the change of permeability of the compacted bentonite (with high- and low-dry density) during alteration under the alkaline conditions. Furthermore, stability of saponite, which has similar physical properties to the bentonite, under the alkaline conditions was also examined. In this report, we show the outline of those research results, and lay out the clarified future issues extracted from our results. Ten clarified future issues were divided three categories as follows: 1) the estimation of the alteration behavior of the bentonite by alkaline solutions, 2) the elucidation of the mechanism of physical properties (e.g., permeability, swelling properties and mechanistic properties) change of the compacted bentonites during alteration, and 3) the development of the model building and simulation technology concerning the change in physical properties during alteration under alkaline conditions. (author)

  9. Gold leaching with elemental sulfur in alkaline solutions under oxygen pressure

    Institute of Scientific and Technical Information of China (English)

    方兆珩; 石伟

    2003-01-01

    A gold leaching process by using oxidation products of elemental sulfur in alkaline solutions was pro-posed and investigated. A gold concentrate and a residue from an arsenic refractory gold concentrate by acidic oxida-tion leaching were tested. The residue contains 16.3% elemental sulfur and no more elemental sulfur was added intests. For the concentrate elemental sulfur was added before leaching tests. The leaching ratio of gold depends main-ly on the initial equivalent ratio of elemental sulfur to hydroxyl ions, the consumption of oxygen and the reactiontemperature in the process. Analysis of the experimental results shows that thiosulfate is the majority complexingreagent for gold in the process. Over 90% gold was leached from the residue and 82%-87% from the concentrate byusing this process.

  10. Galvanic Corrosion between Alloy 690 and Magnetite in Alkaline Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Soon-Hyeok Jeon

    2015-12-01

    Full Text Available The galvanic corrosion behavior of Alloy 690 coupled with magnetite has been investigated in an alkaline solution at 30 °C and 60 °C using a potentiodynamic polarization method and a zero resistance ammeter. The positive current values were recorded in the galvanic couple and the corrosion potential of Alloy 690 was relatively lower. These results indicate that Alloy 690 behaves as the anode of the pair. The galvanic coupling between Alloy 690 and magnetite increased the corrosion rate of Alloy 690. The temperature increase led to an increase in the extent of galvanic effect and a decrease in the stability of passive film. Galvanic effect between Alloy 690 and magnetite is proposed as an additional factor accelerating the corrosion rate of Alloy 690 steam generator tubing in secondary water.

  11. Determination of Salt Impurities in MDEA Solution Used in Desulfurization of Highly Sulphurous Natural Gas

    Institute of Scientific and Technical Information of China (English)

    Liu Yucheng; Zhang Bo; Chen Mingyan; Wu Danni; Zhou Zheng

    2015-01-01

    The foaming phenomenon of N-methyldiethanolamine (MDEA) solution used in desulfurization process occurs frequently in the natural-gas puriifcation plant. The foaming phenomenon has a strong impact on operation of the process unit. The salt impurities are the main reason for causing the foaming of MDEA solution, so the full analysis of salt impuri-ties is necessary. A method for comprehensive analysis of salt impurities in MDEA solution used in desulfurization process was established. Anions and non-metallic cations of MDEA solution were determined by different conditions of ion chro-matograph, respectively. Metallic cations of the solution were detected by atomic absorption spectrophotometer with the N2O-C2H2 lfame absorption. The analytical results of salt impurities in the desulfurization solution can provide a theoretical basis for an accurate analysis of the factors affecting the foaming of MDEA to unveil further control measures.

  12. Effects of Various Mixed Salt-Alkaline Stress Conditions on Seed Germination and Early Seedling Growth of Leymus chinensis from Songnen Grassland of China

    Directory of Open Access Journals (Sweden)

    Jixiang LIN

    2014-06-01

    Full Text Available Soil salinization and alkalization always co-occur in grassland ecosystem, but little information exists concerning the mixed effects of salt-alkaline stresses on plants.Leymus chinensis is considered as one of the most promising grass species in Songnen Grassland of Northern China. In this study, we investigated the effects of 30 mixed salt-alkaline conditions (NaCl, Na2SO4, NaHCO3 and Na2CO3; pH 7.10-10.18 and salinity 50-250 mM on seed germination and seedling growth of L. chinensis. The results showed that germination percentage and rate were both decreased with increasing salinity and pH. Nongerminated seeds germinated well after being transferred to distilled water from treatment groups. Shoot and radicle growth were also affacted by salinity, pH and their interactions. However, radicle length decreased more markedly with increasing salinity and pH, and was strongly inhibited when pH reached 8.05. Stepwise regression analysis results showed that salinity was the dominant factor for seed germination under mixed salt-alkaline stress conditions. However, once radicle break through the seed coat, and pH changed into the dominant factor for seedling establishment. These results indicated that mixed salt-alkaline stresses had different impacts on germination and early seedling stages of L. chinensis. A better understanding of the germination and seedling processes should facilitate the effective utilization of this species under such complex environment.

  13. Reactive transport modeling of column experiments on the evolution of saline-alkaline waste solutions.

    Science.gov (United States)

    Zheng, Zuoping; Zhang, Guoxiang; Wan, Jiamin

    2008-04-01

    Leakage of saline-alkaline tank waste solutions often creates a serious environmental contamination problem. To better understand the mechanisms controlling the fate of such waste solutions in the Hanford vadose zone, we simulated reactive transport in columns designed to represent local site conditions. The Pitzer ion interaction module was used, with principal geochemical processes considered in the simulation including quartz dissolution, precipitation of brucite, calcite, and portlandite, multi-component cation exchange, and aqueous complexation reactions. Good matches were observed between the simulated and measured column data at ambient temperature ( approximately 21 degrees C). Relatively good agreement was also obtained at high temperature ( approximately 70 degrees C). The decrease of pH at the plume front is examined through formation of secondary mineral phases and/or quartz dissolution. Substantial formation of secondary mineral phases resulting from multi-component cation exchange suggests that these phases are responsible for a decrease in pH within the plume front. In addition, a sensitivity analysis was conducted with respect to cation exchange capacity, selectivity coefficient, mineral assemblage, temperature, and ionic strength. This study could serve as a useful guide to subsequent experimental work, to thermodynamic models developed for the concentrated solutions at high ionic strength and to other types of waste plume studies. PMID:18313795

  14. Reactive transport modeling of column experiments on the evolution of saline alkaline waste solutions

    Science.gov (United States)

    Zheng, Zuoping; Zhang, Guoxiang; Wan, Jiamin

    2008-04-01

    Leakage of saline-alkaline tank waste solutions often creates a serious environmental contamination problem. To better understand the mechanisms controlling the fate of such waste solutions in the Hanford vadose zone, we simulated reactive transport in columns designed to represent local site conditions. The Pitzer ion interaction module was used, with principal geochemical processes considered in the simulation including quartz dissolution, precipitation of brucite, calcite, and portlandite, multi-component cation exchange, and aqueous complexation reactions. Good matches were observed between the simulated and measured column data at ambient temperature (˜ 21 °C). Relatively good agreement was also obtained at high temperature (˜ 70 °C). The decrease of pH at the plume front is examined through formation of secondary mineral phases and/or quartz dissolution. Substantial formation of secondary mineral phases resulting from multi-component cation exchange suggests that these phases are responsible for a decrease in pH within the plume front. In addition, a sensitivity analysis was conducted with respect to cation exchange capacity, selectivity coefficient, mineral assemblage, temperature, and ionic strength. This study could serve as a useful guide to subsequent experimental work, to thermodynamic models developed for the concentrated solutions at high ionic strength and to other types of waste plume studies.

  15. The cathodic reduction of dioxygen on uranium oxide in dilute alkaline aqueous solution

    International Nuclear Information System (INIS)

    The cathodic reduction of dioxygen on uranium oxide in dilute alkaline aqueous solutions has been investigated within the context of a program to develop a comprehensive model to predict the behaviour of used CANDU (Canada Deuterium Uranium) nuclear fuel under disposal-vault conditions. Two different kinds of ceramic UO2 were studied: reactor-grade CANDU fuel with normal p-type electrical conductivity and low-resistance material that exhibits n-type photoelectrochemical behaviour. The transport of electroactive species in solution was controlled by varying the rotation rate of rotating disc electrodes (RDE) and rotating ring-disc electrodes (RRDE). Steady-state polarization measurements were made using the current-interrupt method to compensate for the potential drop caused by ohmic resistance. Any release of peroxide to solution from the UO2 (disc) surface could be monitored by oxidizing it at the Au ring of an RRDE. The existing theory for the cathodic 02-reduction process as applied to RDE and RRDE experiments has been reviewed as a starting point for the interpretation of the results obtained in our work. (37 figs., 2 tabs., 170 refs.)

  16. Salt weathering in Egyptian limestone after laboratory simulations with continuous flow of salt solutions at different temperatures

    Science.gov (United States)

    Aly, Nevin; Gomez-Heras, Miguel; Hamed, Ayman; Alvarez de Buergo, Monica

    2013-04-01

    weathering in Egyptian limestone after laboratory simulations with continuous flow of salt solutions at different temperatures Nevin Aly Mohamed (1), Miguel Gomez - Heras(2), Ayman Hamed Ahmed (1), and Monica Alvarez de Buergo(2). (1) Faculty of Pet. & Min. Engineering- Suez Canal University, Suez, Egypt, (2) Instituto de Geociencias (CSIC-UCM) Madrid. Spain. Limestone is one of the most frequent building stones in Egypt and is used since the time of ancient Egyptians and salt weathering is one of the main threats to its conservation. Most of the limestone used in historical monuments in Cairo is a biomicrite extracted from the Mid-Eocene Mokattam Group. During this work, cylindrical samples (2.4 cm diameter and approx. 4.8 cm length) were subjected, in a purpose-made simulation chamber, to simulated laboratory weathering tests with fixed salt concentration (10% weight NaCl solution), at different temperatures, which were kept constant throughout each test (10, 20, 30, 40 oC). During each test, salt solutions flowed continuously imbibing samples by capilarity. Humidity within the simulation chamber was reduced using silica gel to keep it low and constant to increase evaporation rate. Temperature, humidity inside the simulation chamber and samples weight were digitally monitored during each test. Results show the advantages of the proposed experimental methodology using a continuous flow of salt solutions and shed light on the effect of temperature on the dynamics of salt crystallization on and within samples. Research funded by mission sector of high education ministry, Egypt and Geomateriales S2009/MAT-1629.

  17. Purification of alkaline solutions and wastes from actinides and technetium by coprecipitation with some carriers using the method of appearing reagents: Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Peretrukhin, V.F.; Silin, V.I.; Kareta, A.V.; Gelis, A.V.; Shilov, V.P.; German, K.E.; Firsova, E.V.; Maslennikov, A.G.; Trushina, V.E. [Russian Academy of Sciences, Moscow (Russian Federation). Inst. of Physical Chemistry

    1998-09-01

    The coprecipitation of transuranium elements (TRU) and technetium from alkaline solutions and from simulants of Hanford Site tank wastes has been studied in reducing and oxidizing conditions on uranium(IV,VI) hydroxocompounds, tetraalkylammonium perrhenate and perchlorate, and on hydroxides of Fe(III), Co(III), Mn(II), and Cr(III) using the method of appearing reagents (MAR). Coprecipitations in alkaline solution have been shown to give high decontamination factors (DF) at low content of carrier and in the presence of high salt concentrations. Uranium(IV) hydroxide in concentrations higher than 3 {times} 10{sup {minus}3} M coprecipitates Pu and Cm in any oxidation state from 0.2 to 4 M NaOH with DFs of 110 to 1000 and Np and Tc with DFs of 51 to 176. Technetium (VII) coprecipitates with (5 to 8) {times} 10{sup {minus}4} M tetrabutylammonium (TBA) perrhenate in 0.01 to 0.02 M TBA hydroxide from 0.5 to 1.5 M NaOH to give DFs of 150 to 200. Coprecipitations of Np and Pu with Co(OH){sub 3}, Fe(OH){sub 3}, Cr(OH){sub 3}, and Mn(OH){sub 2} obtained by the MAR from precursors in the range from pH 10.5 to 0.4 M NaOH give DFs from 80 to 400.

  18. Solubility and speciation of actinides in salt solutions and migration experiments of intermediate level waste in salt formations

    International Nuclear Information System (INIS)

    A comprehensive study into the solubility of the actinides americium and plutonium in concentrated salt solutions, the release of radionuclides from various forms of conditioned ILW and the migration behaviour of these nuclides through geological material specific to the Gorleben site in Lower Saxony is described. A detailed investigation into the characterization of four highly concentrated salt solutions in terms of their pH, Eh, inorganic carbon contents and their densities is given and a series of experiments investigating the solubility of standard americium(III) and plutonium(IV) hydroxides in these solutions is described. Transuranic mobility studies for solutions derived from the standard hydroxides through salt and sand have shown the presence of at least two types of species present of widely differing mobility; one migrating with approximately the same velocity as the solvent front and the other strongly retarded. Actinide mobility data are presented and discussed for leachates derived from the simulated ILW in cement and data are also presented for the migration of the fission products in leachates derived from real waste solidified in cement and bitumen. Relatively high plutonium mobilities were observed in the case of the former and in the case of the real waste leachates, cesium was found to be the least retarded. The sorption of ruthenium was found to be largely associated with the insoluble residues of the natural rock salt rather than the halite itself. (orig./RB)

  19. Addition and elimination kinetics in OH radical induced oxidation of phenol and cresols in acidic and alkaline solutions

    International Nuclear Information System (INIS)

    The rates of the two consecutive reactions, OH radical addition and H2O/OH- elimination, were studied by pulse radiolysis in highly acidic (pH=1.3-1.9) and alkaline (pH∼11) solutions, respectively, for phenol and for the three cresol isomers. The rate coefficient of the addition as measured by the build-up of phenoxyl radical absorbance and by a competitive method is the same (1.4±0.1)x1010 mol-1 dm3 s-1 both in acidic and alkaline solution. The rate coefficient of the H2O elimination in acidic solution is (1.6±0.2)x106 s-1, whereas the coefficient of the OH- elimination in alkaline solutions is 6-8 times higher. The kinetics of the phenoxyl radical formation was described by the two-exponential equation of the consecutive reactions: the first exponential is related to the pseudo-first-order addition, while the second to the elimination reaction. No considerable structure dependence was found in the rate coefficients, indicating that the methyl substitutent in these highly acidic or alkaline solutions influences neither the addition nor the elimination rate

  20. Technetium in alkaline, high-salt, radioactive tank waste supernate: Preliminary characterization and removal

    International Nuclear Information System (INIS)

    This report describes the initial work conducted at Pacific Northwest National Laboratory to study technetium (Tc) removal from Hanford tank waste supernates and Tc oxidation state in the supernates. Filtered supernate samples from four tanks were studied: a composite double shell slurry feed (DSSF) consisting of 70% from Tank AW-101, 20% from AP-106, and 10% from AP-102; and three complexant concentrate (CC) wastes (Tanks AN-107, SY-101, ANS SY-103) that are distinguished by having a high concentration of organic complexants. The work included batch contacts of these waste samples with Reillex trademark-HPQ (anion exchanger from Reilly Industries) and ABEC 5000 (a sorbent from Eichrom Industries), materials designed to effectively remove Tc as pertechnetate from tank wastes. A short study of Tc analysis methods was completed. A preliminary identification of the oxidation state of non-pertechnetate species in the supernates was made by analyzing the technetium x-ray absorption spectra of four CC waste samples. Molybdenum (Mo) and rhenium (Re) spiked test solutions and simulants were tested with electrospray ionization-mass spectrometry to evaluate the feasibility of the technique for identifying Tc species in waste samples

  1. Measurement of linear attenuation coefficients of gamma rays for some salts by aqueous solution method

    International Nuclear Information System (INIS)

    The linear attenuation coefficients of dilute aqueous solutions of some salts with varying concentrations are measured for different gamma energies (0.36 MeV to 1.33 MeV). From these measurements, linear attenuation coefficients for pure salts are obtained by using the improved technique of Teli (1998). The comparison with theoretical values shows excellent agreement. Half value thicknesses of the salts and total atomic cross sections are also evaluated. (author)

  2. Reactivity of the cement-bentonite interface with alkaline solutions using transport cells

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez, Raul [Dpto. Quimica Agricola, Geologia y Geoquimica, Facultad de Ciencias, Universidad Autonoma de Madrid, Campus Cantoblanco, 28049 Madrid (Spain); Cuevas, Jaime [Dpto. Quimica Agricola, Geologia y Geoquimica, Facultad de Ciencias, Universidad Autonoma de Madrid, Campus Cantoblanco, 28049 Madrid (Spain)]. E-mail: jaime.cuevas@uam.es; Sanchez, Laura [Dpto. Quimica Agricola, Geologia y Geoquimica, Facultad de Ciencias, Universidad Autonoma de Madrid, Campus Cantoblanco, 28049 Madrid (Spain); Villa, Raquel Vigil de la [Dpto. Quimica Agricola, Geologia y Geoquimica, Facultad de Ciencias, Universidad Autonoma de Madrid, Campus Cantoblanco, 28049 Madrid (Spain); Leguey, Santiago [Dpto. Quimica Agricola, Geologia y Geoquimica, Facultad de Ciencias, Universidad Autonoma de Madrid, Campus Cantoblanco, 28049 Madrid (Spain)

    2006-06-15

    Clayey formations are considered as suitable host rocks to develop a Deep Geological Repository (DGR) for nuclear wastes. A concrete ring, located between the clayey formation and the bentonite barrier, is needed as structural support for the galleries. This material will act as a source of alkaline fluids when the formation's pore water saturates the system. This investigation evaluates the performance of the concrete-bentonite system by means of both geochemical codes and experimental results. A column made of compacted bentonite from La Serrata (Almeria, Spain) (1.4 g/cm{sup 3}, dry density) was held in contact with an ordinary Portland cement (OPC) mortar. Two alkaline solutions (Ca(OH){sub 2} saturated and NaOH 0.25 M) were injected from the mortar's side at 25, 60 and 120 deg. C. The permeability of the system and the effluent fluid composition were determined periodically. Finally, the solid phase was sampled and analyzed after 1 year of treatment. Ca(OH){sub 2} saturated fluids does not alter the mineralogy over the experiment time scale. NaOH fluids produced minor changes at 60-25 deg. C but at 120 deg. C a thin tobermorite layer of 1.5 mm precipitates in the clay aggregate surfaces at the interface. After this layer, analcime nucleates in heterogeneous patches affecting the whole compacted bentonite probe (2 cm thickness). The use of the PHREEQC code thermodynamic approach predicts the mineralogical transformations. However, it is necessary to introduce kinetic laws and to consider the existence of stagnant zones in the model in order to simulate the heterogeneous spatial alteration observed.

  3. Modeling experimental results of diffusion of alkaline solutions through a compacted bentonite barrier

    International Nuclear Information System (INIS)

    The interaction between concrete/cement and swelling clay (bentonite) has been modeled in the context of engineered barrier systems for deep geological disposal of high-level radioactive waste. The geochemical transformations observed in laboratory diffusion experiments at 60 and 90 oC between bentonite and different high-pH solutions (K-Na-OH and Ca(OH)2-saturated) were reconciled with the reactive transport code CrunchFlow. For K-Na-OH solutions (pH = 13.5 at 25 oC) partial dissolution of montmorillonite and precipitation of Mg-silicates (talc-like), hydrotalcite and brucite at the interface are predicted at 60 oC, while at 90 oC the alteration is wider. Alkaline cations diffused beyond the mineralogical alteration zone by means of exchange with Mg2+ in the interlayer region of montmorillonite. Very slow reactivity and minor alteration of the clay are predicted in the Ca(OH)2-bentonite system. The model is a reasonable description of the experiments but also demonstrates the difficulties in modeling processes operating at a small scale under a diffusive regime.

  4. Oxygen reduction at platinum nanoparticles supported on carbon cryogel in alkaline solution

    Directory of Open Access Journals (Sweden)

    N. R. ELEZOVIC

    2007-07-01

    Full Text Available The oxygen reduction reaction was investigated in 0.1 M NaOH solution, on a porous coated electrode formed of Pt particles supported on carbon cryogel. The Pt/C catalyst was characterized by the X-ray diffraction (XRD, transmission electron microscopy (TEM and cyclic voltammetry techniques. The results demonstrated a successful reduction of Pt to metallic form and homogenous Pt particle size distribution with a mean particle size of about 2.7 nm. The ORR kinetics was investigated by linear sweep polarization at a rotating disc electrode. The results showed the existence of two E – log j regions, usually referred to polycrystalline Pt in acid and alkaline solution. At low current densities (lcd, the Tafel slope was found to be close to –2.3RT/F, while at high current densities (hcd it was found to be close to –2×2.3RT/F. It is proposed that the main path in the ORR mechanism on Pt particles was the direct four-electron process, with the transfer of the first electron as the rate determining step. If the activities are expressed through the specific current densities, a small enhancement of the catalytic activity for Pt/C was observed compared to that of polycrystalline Pt. The effect of the Pt particle size on the electrocatalysis of oxygen reduction was ascribed to the predominant (111 facets of the platinum crystallites.

  5. Establishing the potential dependent equilibrium oxide coverage on platinum in alkaline solution and its influence on the oxygen reduction

    DEFF Research Database (Denmark)

    Wiberg, Gustav; Arenz, Matthias

    2012-01-01

    Publication year: 2012 Source:Journal of Power Sources, Volume 217 Gustav K.H. Wiberg, Matthias Arenz The oxidation process of polycrystalline platinum subjected to alkaline solution is re-examined using a combination of cyclic voltammetry and potential hold techniques in Ar, H2 and O2 purged 0.1 M...

  6. Separation of radiostrontium from alkaline reprocessing waste solution using a fixed-bed column of chelating iminodiacetic acid resin

    International Nuclear Information System (INIS)

    A fixed-bed ion exchange column filled with a chelating resin containing iminodiacetic acid functional groups has been tested for removal of strontium from simulated alkaline reprocessing waste solution. The breakthrough curve has been established. Column loading performance is correlated with batch equilibration results. The loaded strontium is eluted in a small volume of 0.5 M HNO3. (author)

  7. Determination of Stoichiometry of Solutes in Molten Salt Solvents by Correlations of Relative Raman Band Intensities

    DEFF Research Database (Denmark)

    Boghosian, Soghomon; Berg, Rolf W.

    1999-01-01

    Raman spectroscopy has been used to determine the stoichiometry of solute complexes in molten salts at high temperatures under static equilibrium conditions, A simple formalism is derived for correlating relative Raman band intensities with stoichiometric coefficients. The experimental procedures...

  8. Temperature effects on geotechnical and hydraulic properties of bentonite hydrated with inorganic salt solutions

    DEFF Research Database (Denmark)

    Rashid, H. M. A.; Kawamoto, K.; Saito, T.;

    2015-01-01

    © 2015, International Journal of GEOMATE. This study investigated the combined effect of temperature and single-species salt solutions on geotechnical properties (swell index and liquid limit) and hydraulic conductivity of bentonite applying different cation types, concentrations, and temperatures...

  9. Potentiometric titration of uranium reduced by chromic salts in chloridic solutions

    International Nuclear Information System (INIS)

    The utilization of chromic salts for reducing the uranium (VI) from chloridic solutions, for potentiometric dosage is described. This method is used in the range of 0,002 to 1,0 M of uranium. (C.G.C.)

  10. Amino acid salt solutions for carbon dioxide capture

    OpenAIRE

    Majchrowicz, Magdalena Elzbieta

    2014-01-01

    Reactive absorption is a common process in the chemical industry and is used, among others, in the treatment of CO2 containing industrial gas streams. The current work was a part of a project with the aim to assess new reactive solvents based on amino acid salts for CO2 removal from industrial gas streams. Initially, a group of promising amino acid salts (taurine, sarcosine, L-proline, -alanine, 6-aminohexanoic acid and DL-methionine) was screened for their CO2 absorption kinetics, pKa value...

  11. Recovery of uranium from the Syrian phosphate by solid-liquid method using alkaline solutions

    International Nuclear Information System (INIS)

    Uranium concentrations were analyzed in the Syrian phosphate deposits. Mean concentrations were found between 50 and 110 ppm. As a consequence, an average phosphate dressing of 22 kg/ha phosphate would charge the soil with 5-20 g/ha uranium when added as a mineral fertilizer. Fine grinding phosphate produced at the Syrian mines was used for uranium recovery by carbonate leaching. The formation of the soluble uranyl tricarbonate anion UO2(CO3)34- permits use of alkali solutions of sodium carbonate and sodium bicarbonate salts for the nearly selective dissolution of uranium from phosphate. Separation of iron, aluminum, titanium, etc., from the uranium during leaching was carried out. Formation of some small amounts of molybdates, vanadates, phosphates, aluminates, and some complexes metal was investigated. This process could be used before the manufacture of TSP fertilizer, and the final products would contain smaller uranium quantities. (author)

  12. Nb-TiO{sub 2} supported platinum nanocatalyst for oxygen reduction reaction in alkaline solutions

    Energy Technology Data Exchange (ETDEWEB)

    Elezovic, N.R., E-mail: nelezovic@tmf.bg.ac.rs [Institute for Multidisciplinary Research, University of Belgrade, Kneza Viseslava 1, Belgrade (Serbia); Babic, B.M. [Vinca Institute of Nuclear Sciences, Belgrade (Serbia); Radmilovic, V.R. [National Center for Electron Microscopy, LBNL University of California, Berkely (United States); Vracar, Lj.M.; Krstajic, N.V. [Faculty of Technology and Metallurgy, University of Belgrade, Belgrade (Serbia)

    2011-10-30

    Highlights: > Nb doped TiO{sub 2} catalyst support was successfully synthesized. > Synthesized support surface area was much higher comparing with sub-stoichiometric titanium oxides as supporting material. > The Nb-TiO{sub 2} supported Pt catalyst was successfully prepared and characterized by TEM technique. > Nb doped TiO{sub 2} support seems to be more suitable than carbon based support. > The change in the rate-determining step was proposed for reaction mechanism explanation. - Abstract: Platinum based nanocatalyst at home made Nb-TiO{sub 2} support was synthesized and characterized as the catalyst for oxygen reduction reaction in 0.1 mol dm{sup -3} NaOH, at 25 deg. C. Nb doped TiO{sub 2} catalyst support, containing 5% of Nb, has been synthesized by modified acid-catalyzed sol-gel procedure in non-aqueous medium. BET and X-ray diffraction (XRD) techniques were applied for characterization of synthesized supporting material. XRD analysis revealed only presence of anatase TiO{sub 2} phase in synthesized support powder. Existence of any peaks belonging to Nb compounds has not been observed, indicating Nb incorporated into the lattice. Nb-TiO{sub 2} supported Pt nanocatalyst synthesized, using borohydride reduction method, was characterized by TEM and HRTEM techniques. Platinum nanoparticles distribution, over Nb doped TiO{sub 2} support, was quite homogenous. Mean particle size of about 4 nm was found with no pronounced particle agglomeration. Electrochemical techniques: cyclic voltammetry and linear sweep voltammetry at rotating disc electrode were applied in order to study kinetics and estimate catalytic activity of this new catalyst for the oxygen reduction reaction in alkaline solution. Two different Tafel slopes were found: one close to -90 mV dec{sup -1} in low current density region and other approximately -200 mV dec{sup -1} in high current density region, which is in good accordance with literature results for oxygen reduction at Pt single crystals, as

  13. A salt-bridge structure in solution revealed by 2D-IR spectroscopy

    Science.gov (United States)

    Huerta-Viga, Adriana; Domingos, Sérgio R.; Amirjalayer, Saeed; Woutersen, Sander

    2014-07-01

    Salt bridges are known to be important for the stability of protein conformation, but up to now it has been difficult to study their geometry in solution. Here we characterize the spatial structure of a model salt bridge between guanidinium (Gdm+) and acetate (Ac-) using two-dimensional vibrational (2D-IR) spectroscopy. We find that as a result of salt bridging the infrared response of Gdm+ and Ac- change significantly, and in the 2D-IR spectrum, salt bridging of the molecules appears as cross peaks. From the 2D-IR spectrum we determine the relative orientation of the transition-dipole moments of the vibrational modes involved in the salt bridge, as well as the coupling between them. In this manner we reconstruct the geometry of the solvated salt bridge.

  14. Structure of a model salt bridge in solution investigated with 2D-IR spectroscopy

    CERN Document Server

    Huerta-Viga, Adriana; Amirjalayer, Saeed; Woutersen, Sander

    2013-01-01

    Salt bridges are known to be important for the stability of protein conformation, but up to now it has been difficult to study their geometry in solution. Here we characterize the spatial structure of a model salt bridge between guanidinium (Gdm+) and acetate (Ac-) using two-dimensional vibrational (2D-IR) spectroscopy. We find that as a result of salt bridging the infrared response of Gdm+ and Ac- change significantly, and in the 2D-IR spectrum, salt bridging of the molecules appears as cross peaks. From the 2D-IR spectrum we determine the relative orientation of the transition-dipole moments of the vibrational modes involved in the salt bridge, as well as the coupling between them. In this manner we reconstruct the geometry of the solvated salt bridge.

  15. Amino acid salt solutions for carbon dioxide capture

    NARCIS (Netherlands)

    Majchrowicz, Magdalena Elzbieta

    2014-01-01

    Reactive absorption is a common process in the chemical industry and is used, among others, in the treatment of CO2 containing industrial gas streams. The current work was a part of a project with the aim to assess new reactive solvents based on amino acid salts for CO2 removal from industrial gas s

  16. Enzymatic methods for the determination of pollution in seawater using salt resistant alkaline phosphatase from eggs of the sea urchin Strongylocentrotus intermedius

    International Nuclear Information System (INIS)

    Highlights: • Alkaline phosphatase from eggs of the sea urchin (StAP) proved to be active in seawater. • Activity of StAP is inhibited by very low concentrations of heavy metal. • A test to assess sea and fresh water quality has been developed basing on StAP. • For the first time a salt resistant alkaline phosphatase has been found in eukaryote. - Abstract: A new salt resistant alkaline phosphatase from eggs of the sea urchin Strongylocentrotus intermedius (StAP) has been shown to have a unique property to hydrolyze substrate in seawater without loss of enzymatic activity. The enzyme has pH optimum at 8.0–8.5. Model experiments showed various concentrations of copper, zinc, cadmium and lead added to seawater or a standard buffer mixture to inhibit completely the enzyme activity at the concentrations of 15–150 μg/l. StAP sensitivity to the presence in seawater of metals, pesticides, detergents and oil products appears to be considerably less. Samples of seawater taken from aquatic areas of the Troitsy Bay of the Peter the Great Bay, Japan Sea have been shown to inhibit the enzyme activity; the same was shown for the samples of fresh waters. The phosphatase inhibition assay developed proved to be highly sensitive, technically easy-to use allowing to test a great number of samples

  17. Critical anomalies of alkaline fading of phenolphthalein in the critical solution of 2-butoxyethanol + water.

    Science.gov (United States)

    Du, Zhongyu; Yin, Handi; Hao, Zhiguo; Zheng, Peizhu; Shen, Weiguo

    2013-12-14

    We have used three-wavelength UV-spectrophotometry to study the reaction of the alkaline fading of phenolphthalein in the critical solution of 2-butoxyethanol + water. It was found that when the temperature was far away from the critical point, the values of the natural logarithm of the rate constant k and the natural logarithm of the chemical equilibrium K determined in our experiments had good linear relationships with the reciprocal of temperature, which served as the backgrounds and were used for correcting k and K in the critical region. The critical slowing down of the reaction and the critical anomaly of the chemical equilibrium were detected near the critical point. The value of the critical exponent characterizing the slowing down effect of the reaction rate was obtained to be 0.156, which was close to the value 0.11 associated with the heat capacity divergence and agreed with the theoretical prediction. The experimental result also confirmed the theoretical prediction of 0.11 for the critical exponent characterizing the weak divergence of the singularity of the chemical equilibrium. PMID:24329072

  18. Ultraviolet spectrum and decay of the ozonide ion radical, O3-, in strong alkaline solution

    International Nuclear Information System (INIS)

    Pulse radiolytic experiments in strong alkaline solution (pH 13-14) on the formation and the decay of the ozonide ion radical, O3-, are reported. The high-pressure cell technique was used applying 4 MPa of nitrous oxide and 0.1 MPa of oxygen. The spectrum of O3- in the uv was measured and the decay product was identified as the peroxy radical ion, O2-. A complete mechanism for the decay of O3- is based on the following reactions: O3- + O- → 2O2- and O2- + O- + H2O → O2 + 2OH-. A computer simulation of the high-pressure system as well as the atmospheric-pressure oxygenated system supports this mechanism and yields a rate constant, k/sub (O3- + O-)/ of (7.0 +- 1.0) x 108 dm3 mol-1s-1. As a consequence of our mechanism, a k/sub (O2- + O-)/ of (6.0 +- 1.0) x 108 dm3 mol-1 s-1 is also derived from the computations

  19. Production of ultrafine zinc powder from wastes containing zinc by electrowinning in alkaline solution

    Directory of Open Access Journals (Sweden)

    Zhao Youcai

    2013-12-01

    Full Text Available Production of ultrafine zinc powder from industrial wastes by electrowinning in alkaline solution was studied. Stainless steel and magnesium electrodes were used as anode and cathode, respectively. Morphology, size distribution and composition of the Zn particles were characterized by Scanning Electron Microscopy, Laser Particle Size Analyzer, and Inductive Coupled Plasma Emission Spectrometer. The required composition of the electrolyte for ultrafine particles was found to be 25-35 g/L Zn, 200-220 g/L NaOH and 20-40 mg/L Pb. The optimal conditions were a current density of 1000-1200 A/m² and an electrolyte temperature of 30-40 °C. The results indicated that the lead additive exerted a beneficial effect on the refining of the particles, by increasing the cathodic polarization. Through this study, ultrafine zinc powder with a size distribution of around 10 μm could be produced, and considerably high current efficiencies (97-99 % were obtained.

  20. Alteration of non-metallic barriers and evolution of solution chemistry in salt formations in Germany

    International Nuclear Information System (INIS)

    Different Engineered Barrier Systems (EBS) materials considered in Germany for the sealing of repositories in salt formations are presented. Their long term behaviour in terms of interactions with salt solutions is discussed and evaluated. The discussed EBS materials are crushed salt, self sealing salt backfill, bentonite and salt concrete. Whereas the knowledge concerning the geochemical, geomechanical, hydrological and thermal behavior of crushed salt and salt concrete is well advanced further research is needed for other EBS materials. The self healing salt backfill has also been investigated in depth recently. In order to fully qualify this material large scale in situ experiments are still needed. The present knowledge on compacted bentonites in a salt environment is not yet sufficient for reliable predictions of the long-term performance in salt formations. The sealing concept of the low- and intermediate-level Radioactive Waste Repository Morsleben (ERAM) in a former rock salt and potash mine is presented. This concept is based on cementitious materials, i.e. salt concrete. The geochemical stability of different salt concretes in contact with brines expected in ERAM is addressed. It is shown how the results from leaching experiments and geochemical modelling are used in the safety analyses and how the chemical boundary conditions prevailing in the EBS influence the development of the permeability of the sealing system and thus control the radionuclide release. As a result of modelling the behaviour of the seals in the safety assessment it is shown, that the seals are corroded within a time span of about 20 000 years. The influence of the uncertainty in the model parameters on the safety of the repository was assessed by a variation of the initial permeability of the seal. The maximum dose rate resulting from the radionuclide release from ERAM is nearly independent of the variation of the initial permeability within four orders of magnitude. (authors)

  1. Heat-induced formation of myosin oligomer-soluble filament complex in high-salt solution.

    Science.gov (United States)

    Shimada, Masato; Takai, Eisuke; Ejima, Daisuke; Arakawa, Tsutomu; Shiraki, Kentaro

    2015-02-01

    Heat-induced aggregation of myosin into an elastic gel plays an important role in the water-holding capacity and texture of meat products. Here, we investigated thermal aggregation of porcine myosin in high-salt solution over a wide temperature range by dynamic light scattering experiments. The myosin samples were readily dissolved in 1.0 M NaCl at 25 °C followed by dilution into various salt concentrations. The diluted solutions consistently contained both myosin monomers and soluble filaments. The filament size decreased with increasing salt concentration and temperature. High temperatures above Tm led to at least partial dissociation of soluble filaments and thermal unfolding, resulting in the formation of soluble oligomers and binding to the persistently present soluble filaments. Such a complex formation between the oligomers and filaments has never been observed. Our results provide new insight into the heat-induced myosin gelation in high-salt solution. PMID:25445683

  2. Effect of alkaline solutions on the tensile properties of glass-polyester pipes

    Directory of Open Access Journals (Sweden)

    Putić Slaviša S.

    2011-01-01

    Full Text Available Construction materials, traditionally used in process equipment, are today successfully replaced by composite materials. Hence, many pipes are made of these materials. The subject of this study was the influence of liquids on the state of stresses and tensile strengths in the longitudinal and circumferential direction of glass-polyester pipes of a definite structure and known fabrication process. These analyses are of great importance for the use of glass-polyester pipes in the chemical industry. The tensile properties (the ultimate tensile strength and the modulus of elasticity were tested and determined for specimens cut out of the pipes; flat specimens for the tensile properties in the longitudinal direction and ring specimens for the tensile properties in the circumferential direction. First, the tension test was performed on virgin samples (without the influence of any liquid, to obtain knowledge about the original tensile properties of the material composite studied. Subsequently, the specimens were soaked in alkaline solutions: sodium hydroxide (strong alkali and ammonium hydroxide (weak alkali. These solutions were selected because of their considerable difference in pH values. The specimens and rings were left for 3, 10, 30 and 60 days in each liquid at room temperature. Then, the samples were tested on tension by the standard testing procedure. A comparison of the obtained results was made based on the pH values of the aggressive media in which the examined material had been soaked, as well as based on the original tensile properties and the number of days of treatment. Micromechanical analyses of sample breakage helped in the elucidation of the influence of the liquids on the structure of the composite pipe and enabled models and mechanisms that produced the change of strength to be proposed.

  3. Development of analytical technique of alteration minerals formed in bentonite by the reaction with alkaline solution

    International Nuclear Information System (INIS)

    Bentonite will be used as a buffer material, according to the TRU waste disposal concept in Japan, to retard radionuclides migration, to restrict seepage of ground water and to filtrate colloids. One of the concern about the buffer material is the long term alteration of bentonite with cementitious material. Long term alteration of bentonite-based materials with alkaline solution has been studied by means of analytical approaches, coupling mass transport and chemical reactions, which suggest changes in various properties of buffer materials. Long term performance assessment of engineered barriers under disposal conditions is important to achieve a reasonable design, eliminating excessive conservatism in the safety assessment. Therefore it is essential for improving the reliance of the performance assessment to verify the analytical results through alteration tests and/or natural analogue. The geochemical analyses indicate that major alteration reactions involve dissolution of portlandite, chalcedony and montmorillonite and formation of C-S-H gel and analcime at the interface between cement and bentonite. However, in the alteration tests assuming interaction between bentonite and cement, secondary minerals due to alteration under the expected condition for geological disposal (equilibrated water with cement at low liquid/solid ratio) had not been observed, though the alteration was observed under accelerated hyper alkaline and high temperatures conditions. The reason is considered that it is difficult to analyze C-S-H gel formed at the interface because of its small quantity. One of examples is the Kunigel V1, a potential buffer material in Japan, which consists of montmorillonite, chalcedony, plagioclase, and calcite. In the XRD analysis of the Kunigel V 1, the locations of the primary peak of the calcite and that of the C-S-H gel overlap, which makes identification of small quantity of C-S-H gel formed as a secondary mineral difficult. Thus development of

  4. The alkaline solution to the emergence of life: energy, entropy and early evolution.

    Science.gov (United States)

    Russell, Michael J

    2007-01-01

    The Earth agglomerates and heats. Convection cells within the planetary interior expedite the cooling process. Volcanoes evolve steam, carbon dioxide, sulfur dioxide and pyrophosphate. An acidulous Hadean ocean condenses from the carbon dioxide atmosphere. Dusts and stratospheric sulfurous smogs absorb a proportion of the Sun's rays. The cooled ocean leaks into the stressed crust and also convects. High temperature acid springs, coupled to magmatic plumes and spreading centers, emit iron, manganese, zinc, cobalt and nickel ions to the ocean. Away from the spreading centers cooler alkaline spring waters emanate from the ocean floor. These bear hydrogen, formate, ammonia, hydrosulfide and minor methane thiol. The thermal potential begins to be dissipated but the chemical potential is dammed. The exhaling alkaline solutions are frustrated in their further attempt to mix thoroughly with their oceanic source by the spontaneous precipitation of biomorphic barriers of colloidal iron compounds and other minerals. It is here we surmise that organic molecules are synthesized, filtered, concentrated and adsorbed, while acetate and methane--separate products of the precursor to the reductive acetyl-coenzyme-A pathway-are exhaled as waste. Reactions in mineral compartments produce acetate, amino acids, and the components of nucleosides. Short peptides, condensed from the simple amino acids, sequester 'ready-made' iron sulfide clusters to form protoferredoxins, and also bind phosphates. Nucleotides are assembled from amino acids, simple phosphates carbon dioxide and ribose phosphate upon nanocrystalline mineral surfaces. The side chains of particular amino acids register to fitting nucleotide triplet clefts. Keyed in, the amino acids are polymerized, through acid-base catalysis, to alpha chains. Peptides, the tenuous outer-most filaments of the nanocrysts, continually peel away from bound RNA. The polymers are concentrated at cooler regions of the mineral compartments through

  5. Degradation of lead-based pigments by salt solutions

    Czech Academy of Sciences Publication Activity Database

    Kotulanová, Eva; Bezdička, Petr; Hradil, David; Hradilová, J.; Švarcová, Silvie; Grygar, Tomáš

    2009-01-01

    Roč. 10, č. 3 (2009), s. 367-378. ISSN 1296-2074 R&D Projects: GA ČR(CZ) GA203/07/1324; GA AV ČR KJB400320602 Institutional research plan: CEZ:AV0Z40320502 Keywords : X-ray microdiffraction * salts * red lead Subject RIV: CA - Inorganic Chemistry Impact factor: 1.505, year: 2009

  6. The reactivity of the electron formed in the radiolysis of aerated alkaline aqueous solutions containing tetracycline hydrochloride, at 77 Ksup(+)

    International Nuclear Information System (INIS)

    The radiolysis of tetracycline hydrochloride dissolved in aerated alkaline aqueous solutions containing 0.1, 0.5 and 1M NaOH at 77 K, followed by ESR is reported. The rate constants for the reactions between the electron and physical or chemical traps which are present in these solutions are calculated. The reactivity of electrons that are formed in the radiolysis of water decreases in the following proportions: physical traps: chemical traps: molecules of water (4.8x10sup(14) : 6.5x10sup(8) : 1.0). The electrons react preferentially with the solute instead of the solvent. (author)

  7. Zeolite for strontium separation from concentrated sodium salt solutions

    International Nuclear Information System (INIS)

    Strontium sorption from solutions with concentration of 5 mol/l sodium chloride on zeolites of different structure is investigated. Synthetic potassium zeolite of the K-G(13) chabasite type is established to be used to purify the solutions given from strontium radionuclides. Capacity of K-G(13) zeolite for strontium in the solution with concentration of 5 mol/l sodium chloride is 0.65 mmol/g

  8. Microcontact printing of indium metal using salt solution 'ink'

    International Nuclear Information System (INIS)

    Poly(dimethlysiloxane) stamps were made from Si masters fabricated using photolithography and anisotropic etching. GaCl3 and In(NO3)3 were microcontact printed onto Si substrates, creating arrays of micron size metal salt deposits. The In(NO3)3 deposits were further processed by annealing in an N2 :H2 (9:1) forming gas environment at 600 deg. C which converted the deposits into In metal. The ability to inexpensively pattern metal arrays on semiconductor surfaces has implications for ohmic contacts and, with additional processing, arrays of semiconductor crystallites for optoelectronic applications

  9. Length Scale Dependence of the Dynamic Properties of Hyaluronic Acid Solutions in the Presence of Salt

    Energy Technology Data Exchange (ETDEWEB)

    Horkay, Ferenc; Falus, Peter; Hecht, Anne-Marie; Geissler, Erik (CNRS-UMR); (NIH); (ILL)

    2010-12-07

    In solutions of the charged semirigid biopolymer hyaluronic acid in salt-free conditions, the diffusion coefficient D{sub NSE} measured at high transfer momentum q by neutron spin echo is more than an order of magnitude smaller than that determined by dynamic light scattering, D{sub DLS}. This behavior contrasts with neutral polymer solutions. With increasing salt content, D{sub DLS} approaches D{sub NSE}, which is independent of ionic strength. Contrary to theoretical expectation, the ion-polymer coupling, which dominates the low q dynamics of polyelectrolyte solutions, already breaks down at distance scales greater than the Debye-Hueckel length.

  10. Length Scale Dependence of the Dynamic Properties of Hyaluronic Acid Solutions in the Presence of Salt

    International Nuclear Information System (INIS)

    In solutions of the charged semirigid biopolymer hyaluronic acid in salt-free conditions, the diffusion coefficient DNSE measured at high transfer momentum q by neutron spin echo is more than an order of magnitude smaller than that determined by dynamic light scattering, DDLS. This behavior contrasts with neutral polymer solutions. With increasing salt content, DDLS approaches DNSE, which is independent of ionic strength. Contrary to theoretical expectation, the ion-polymer coupling, which dominates the low q dynamics of polyelectrolyte solutions, already breaks down at distance scales greater than the Debye-Hueckel length.

  11. Preparation of silver nanoparticles in solution from a silver salt by laser irradiation.

    Science.gov (United States)

    Abid, J P; Wark, A W; Brevet, P F; Girault, H H

    2002-04-01

    A new method is proposed for the fabrication of a well-defined size and shape distribution of silver nanoparticles in solution; the method employs direct laser irradiation of an aqueous solution containing a silver salt and a surfactant in the absence of reducing agents. PMID:12119726

  12. Amino acid salt solutions as solvents in CO2 capture from flue gas

    DEFF Research Database (Denmark)

    Lerche, Benedicte Mai; Thomsen, Kaj; Stenby, Erling Halfdan

    solutions is their ability to form solid precipitates upon the absorption of CO2. The occurrence of crystallization offers the possibility of increasing the CO2 loading capacity of the solvent. However, precipitation can also have negative effect on the CO2 capture process. The chemical nature of the solid...... loading capacity of aqueous solutions of the potassium salts of selected amino-acids (glycine, taurine, lysine proline, and glutamic acid) were examined, and the relation between the initial amino acid salt concentration and precipitation ability of each solution were determined. Experiments were...... glycine, taurine, and lysine, while in the case of proline, and glutamic acid, the precipitate was found to be bicarbonate. These results give an important contribution to further understanding the potential of amino acid salt solutions in CO2 capture from flue gas....

  13. Release of fission products from oxidised zircaloy cladding in contact with an alkaline solution

    International Nuclear Information System (INIS)

    Before nuclear spent fuel reprocessing, the cladding tubes are sectioned into pieces called hulls in order to release the UO2 pellets. The hulls are collected as solid wastes and were embedded inside a concrete structure until 1995. In the perspective of geological storage, a great interest is given to iodine release during contact between hulls and basic water infiltrated inside the concrete structure. Experiments were performed on zircaloy or zirconium oxidised samples representative of oxidised hulls surfaces. Corrosion tests were performed in autoclave. The specimens were exposed to a basic solution at 250 deg C, 275 deg C and 300 deg C. The corrosion tests were conducted during 12 weeks with regular sampling every two weeks. The partial dissolution of the oxide coating was studied using the rare earth europium element as a surface marker of zirconia. Such a choice is based on experimental results ensuring that this marker will not diffuse in the 250-300 deg C temperature range. Europium was introduced by ion implantation (Rp = 42 nm). The evolutions of europium concentration profiles measured at each corrosion step show that a non homogeneous dissolution of zirconia occurs in this alkaline medium. The mean dissolution rate is equal to 1 nm/day at 300 deg C. In order to analyse the mechanism involved in iodine migration, iodine atoms were introduced in samples by ion implantation. The iodine profile evolution allows to identify two steps in iodine release. A rapid desorption which could not be related to zirconia dissolution and then a stabilisation as far as low the iodine concentration (0.3 at.%) were reached. We demonstrated that hydrogen (representative of hydroxyl) migration in zirconia is clearly enhanced by the presence of iodine in the sample and that the iodine release is correlated to that of hydroxyl ions. The correlation of the behaviour between iodine and hydroxyl ions could be explained by the creation of complexes. (author)

  14. The oxygen evolution reaction on passive oxide covered transition metal electrodes in alkaline solution. Part 2-Cobalt.

    OpenAIRE

    LYONS, MICHAEL EDWARD

    2008-01-01

    Details are outlined of an electrochemical investigation of the oxygen evolution reaction (OER) at passive oxide covered polycrystalline Co electrodes in aqueous alkaline solution. Kinetic studies on electrodes subjected to different pre-treatment routines, yielded different values of the Tafel slope and the reaction order with respect to OH- activity. Only one mechanistic pathway could account for all observed values of these kinetic parameters. This pathway is similar, although ...

  15. The oxygen evolution reaction on passive oxide covered transition metal electrodes in alkaline solution. Part III - Iron.

    OpenAIRE

    LYONS, MICHAEL EDWARD

    2008-01-01

    The kinetics of the oxygen evolution reaction (OER) at passive oxide covered polycrystalline Fe electrodes in aqueous alkaline solution were examined using both dc steady state polarisation and ac impedance techniques. It proved difficult to obtain reproducible polarisation data for bright anodes, and so an electrochemical pre-treatment routine was devised. Upon ageing of a given electrode specimen, and with application of the pre-treatment regime before each experiment, it was po...

  16. The oxygen evolution reaction on passive oxide covered transition metal electrodes in aqueous alkaline solution. Part 1 - Nickel

    OpenAIRE

    LYONS, MICHAEL EDWARD

    2008-01-01

    Various aspects of the oxygen evolution reaction (OER) at passive oxide covered polycrystalline Ni electrodes in aqueous alkaline solution were investigated using electrochemical techniques. Steady state polarisation and electrochemical impedance spectroscopy (EIS) were used to measure kinetically significant parameters including the Tafel slope and the reaction order with respect to OH- activity. While reproducible values of the Tafel slope were readily observed, the recorded cur...

  17. Effectiveness of the squeezing out and final squeezing out of petroleum of an increased viscosity by alkaline solutions

    Energy Technology Data Exchange (ETDEWEB)

    Begnazarov, T.

    1979-01-01

    The remaining petroleum in the flooded zone is determined by the ratio of viscosity forces to the forces of the surface tension, which are expressed by the coefficient Ka. With this, for each kind of porous medium, there exists a natural cricial value Ka. For the purpose of studying the effect of the given parameters on the value of the remaining petroleum, experiments were carried out on artificial specimens. In the tests, using petroleum of the Mishkin deposit, the surface tension on the boundary of the petroleum with the distilled water and alkaline solutions were respectively equal to 37.1 and 1.33 dynes per centimeter. The experiments showed, that the squeezing out of the petroleum with water or alkaline solutions leads to similar results. This means, that the composite parameter Ka does not affect the value of the remaining petroleum saturation. The effectiveness of the final squeezing out of the petroleum of increased viscosity was also studied. These experiments were carried out in two variations of the injection of the squeezed out agent: in the first variation, the petroleum was squeezed out with water in the first stage, and in the second stage it was squeezed out by an alkaline solution, and in the subsequent stages, a change in the squeezing out agent took place. By finishing the first stage, the attained values of the coefficients of the squeezing out were practically similar (0.72). In the second stage, the final squeezing out of the petroleum with a solution of alkaline, provided a major effect.

  18. 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.

  19. Alkali and alkaline earth metal salts of boron anionic complexes with o-hydroxy-benzyl alcohols (saligenin)

    International Nuclear Information System (INIS)

    Salts of two anionic boron complexes with 2 hydroxy-benzyl alcohol-[BA2- and [B(OH)2A]- - were synthesized. The first complex was separated in the form of anhydrous potassium and cesium salts, the second one - in the form of sodium (dihydrate), calcium (dihydrate) and barium (tetrahydrate and anhydrous salt) salts. Conditions of formation are discussed. Solubility in water and organic solvents, interplanar distances of crystal lattice were determined. The compounds were studied by the methods of infrared spectroscopy, thermal analysis. Hypothetical composition of the compounds is given

  20. Fluid-loading solutions and plasma volume: Astro-ade and salt tablets with water

    Science.gov (United States)

    Fortney, Suzanne M.; Seinmann, Laura; Young, Joan A.; Hoskin, Cherylynn N.; Barrows, Linda H.

    1994-01-01

    Fluid loading with salt and water is a countermeasure used after space flight to restore body fluids. However, gastrointestinal side effects have been frequently reported in persons taking similar quantities of salt and water in ground-based studies. The effectiveness of the Shuttle fluid-loading countermeasure (8 gms salt, 0.97 liters of water) was compared to Astro-ade (an isotonic electrolyte solution), to maintain plasma volume (PV) during 4.5 hrs of resting fluid restriction. Three groups of healthy men (n=6) were studied: a Control Group (no drinking), an Astro-ade Group, and a Salt Tablet Group. Changes in PV after drinking were calculated from hematocrit and hemoglobin values. Both the Salt Tablet and Astro-ade Groups maintained PV at 2-3 hours after ingestion compared to the Control Group, which had a 6 percent decline. Side effects (thirst, stomach cramping, and diarrhea) were noted in at least one subject in both the Astro-ade and Salt Tablet Groups. Nausea and vomiting were reported in one subject in the Salt Tablet Group. It was concluded that Astro-ade may be offered as an alternate fluid-loading countermeasure but further work is needed to develop a solution that is more palatable and has fewer side effects.

  1. Laser etching of metals in neutral salt solutions

    Science.gov (United States)

    Datta, M.; Romankiw, L. T.; Vigliotti, D. R.; von Gutfeld, R. J.

    1987-12-01

    We report new findings that relate to rapid maskless laser etching of steel and stainless steel in neutral solutions of sodium chloride, sodium nitrate, and potassium sulfate. Etch rates have been determined as a function of laser power, laser on-time, and solution concentration. The morphology of laser-etched holes obtained in these solutions was compared with holes obtained in pure water. Results indicate that some controlled melting occurs under certain laser conditions in addition to the metal dissolution process induced by the locally intense heat of the laser beam.

  2. CO2 Capture from Flue Gas using Amino Acid Salt Solutions

    DEFF Research Database (Denmark)

    Lerche, Benedicte Mai; Stenby, Erling Halfdan; Thomsen, Kaj

    2009-01-01

    The reversible absorption of CO2 into a chemical solvent is currently the leading CO2 capture technology. Available solvents are almost exclusively based on aqueous alkanolamine solutions, which entail both economic and environmental complications, making the commercialization of the technology...... difficult. Amino acid salt solutions have emerged as an alternative to the alkanolamine solutions. A number of advantages make amino acid salt solutions attractive solvents for CO2 capture from flue gas. In the present study CO2 absorption in aqueous solutions of 0.5 M potassium glycinate and 0.5 M...... monoethanolamine (MEA) were performed, using a stirred cell reactor experimental setup. The absorption of gas containing 10 mol % CO2 and 90 mol % N2 was followed by measuring the percentage of CO2 in the outlet gas. Also the temperature and pH in the solutions were measured during the absorption. The results...

  3. Surface Crystallization of Aqueous Salt Solution Under Overheating and Overcooling

    Directory of Open Access Journals (Sweden)

    Nakoryakov Vladimir

    2016-01-01

    Full Text Available The investigation of the surface crystallization with low negative and high positive temperatures were carried in the paper. Crystallization curves for distillate (Ts0 = −9 °C and different mass salt concentrations NaCl (Ts0 = 80 °C were obtained. Experimental data indicate that the crystallization centers influence each other and the number of centers does not change with time. The maximum speeds for the crystallization front reached 0.3–0.5 m/s. There are a significant anisotropy and a curvature of crystallization front. The surface kinetics should be considered to clarify the rate of freezing and melting of ice in modeling global warming.

  4. Mechanisms of combined effects of salt and alkaline stresses on seed germination and seedlings of melilotus officials (fabaceae) in northeast of china

    International Nuclear Information System (INIS)

    In line with the salt-alkalinized soils found in the northeast of China, the conditions were simulated to investigate the mechanisms associated with this combination of stresses on Melilotus officinalis. The effects of salinity (NaCl: 0-300mM) in combination with alkali (pH: 7.1-9.8) on the seed germination and seedlings of M. officinalis were investigated. The results showed that germination was not inhibited completely by the salt-alkali conditions tested. The recovery germinations were significant higher than the control or had no significant differences with the control under the conditions of NaCl less than 200mM and pH=9.0, suggesting that non-germinated seeds may have a strategy to get through and resist the stress during germination stage. For the seedling growth, M. officinalis was capable of surviving at high pH (pH=9.8) and the salinity (NaCl=200mM) (seedling survival rate: 84.77 ± 8.62 percentage). The characteristic feature for combined salt-alkali stresses is the reciprocal enhancement between salt and alkali stresses. The combined action of salinity and pH should be considered when evaluating the effects of salt-alkali stresses. Correlation and regression analyses showed that salinity was the dominant stress factor, while pH was a secondary factor. From the physiological and ecological parameters, we suggested that M. officinalis is a salt-alkali tolerant species which can be used in vegetative restoration of saline soils in the northeast of China. (author)

  5. On the attenuation of X-rays and gamma-rays for aqueous solutions of salts

    CERN Document Server

    Teli, M T

    1998-01-01

    Disparities in the linear attenuation coefficients of X-rays and gamma rays for aqueous solutions of soluble salts arising from the nonequality of volume of the solution with the sum of volumes of its components are analysed and the mixture rule is reformulated. The disparities are illustrated for NaCl solution for concentrations c=0 to 1 gm/cm sup 3 which indicates that the mixture rule of Teli et al. works well within generally acceptable limits.

  6. Continuous electrolytic decarbonation and recovery of a carbonate salt solution from a metal-contaminated carbonate solution.

    Science.gov (United States)

    Kim, Kwang-Wook; Kim, Yeon-Hwa; Lee, Se-Yoon; Lee, Eil-Hee; Song, Kyusuk; Song, Kee-Chan

    2009-11-15

    This work studied the characteristic changes of a continuous electrolytic decarbonation and recovery of a carbonate salt solution from a metal-contaminated carbonate solution with changes of operational variables in an electrolytic system which consisted of a cell-stacked electrolyzer equipped with a cation exchange membrane and a gas absorber. The system could completely recover the carbonate salt solution from a uranyl carbonato complex solution in a continuous operation. The cathodic feed rate could control the carbonate concentration of the recovered solution and it affected the most transient pH drop phenomenon of a well type within the gas absorber before a steady state was reached, which caused the possibility of a CO(2) gas slip from the gas absorber. The pH drop problem could be overcome by temporarily increasing the OH(-) concentration of the cathodic solution flowing down within the gas absorber only during the time required for a steady state to be obtained in the case without the addition of outside NaOH. An overshooting peak of the carbonate concentration in the recovered solution before a steady state was observed, which was ascribed to the decarbonation of the initial solution filled within the stacked cells by a redundant current leftover from the complete decarbonation of the feeding carbonate solution. PMID:19604641

  7. Extraction of tungsten from bicarbonate solutions by MTAA salts

    International Nuclear Information System (INIS)

    Results are presented on investigations of tungsten extraction from bicarbonate reextracts prepared during reprocessing of carbonate solutions of autoclave-carbonate leaching of mineral raw material and so through ammonium reextraction of polymeric tungsten compounds with preparation of concentrated by tungsten reextracts for separation of conditioned ammonium paratungstate. Variants of proposed technological scheme are discussed

  8. Dynamic flow method to study the CO2 loading capacity of amino acid salt solutions

    DEFF Research Database (Denmark)

    Lerche, Benedicte Mai; Stenby, Erling Halfdan; Thomsen, Kaj

    Due to a number of advantages amino acid salt solutions have emerged as alternatives to the alkanolamine solvents for the chemical absorption of CO2 from flue gas. The use of amino acids in CO2 capture is a bio-mimetic process, as it is similar to CO2 binding by proteins in the blood, such as...... hemoglobin. Amino acid salt solutions have the same amine functionality as alkanolamines, and are thus expected to behave similar towards CO2 in flue gas. Despite rising interest, few studies have been performed so far on amino acids as CO2 absorbents....

  9. Research of measurement errors caused by salt solution temperature drift in surface plasmon resonance sensors

    Institute of Scientific and Technical Information of China (English)

    Yingcai Wu; Zhengtian Gu; YifangYuan

    2006-01-01

    @@ Influence of temperature on measurement of surface plasmon resonance (SPR) sensor was investigated.Samples with various concentrations of NaCI were tested at different temperatures. It was shown that if the affection of temperature could be neglected, measurement precision of salt solution was 0.028 wt.-%.But measurement error of salinity caused by temperature was 0.53 wt.-% in average when the temperature drift was 1 ℃. To reduce the error, a double-cell SPR sensor with salt solution and distilled water flowing respectively and at the same temperature was implemented.

  10. Redox condition in molten salts and solute behavior: A first-principles molecular dynamics study

    Science.gov (United States)

    Nam, Hyo On; Morgan, Dane

    2015-10-01

    Molten salts technology is of significant interest for nuclear, solar, and other energy systems. In this work, first-principles molecular dynamics (FPMD) was used to model the solute behavior in eutectic LiCl-KCl and FLiBe (Li2BeF4) melts at 773 K and 973 K, respectively. The thermo-kinetic properties for solute systems such as the redox potential, solute diffusion coefficients and structural information surrounding the solute were predicted from FPMD modeling and the calculated properties are generally in agreement with the experiments. In particular, we formulate an approach to model redox energetics vs. chlorine (or fluorine) potential from first-principles approaches. This study develops approaches for, and demonstrates the capabilities of, FPMD to model solute properties in molten salts.

  11. A salt-bridge structure in solution revealed by 2D-IR spectroscopy.

    Science.gov (United States)

    Huerta-Viga, Adriana; Domingos, Sérgio R; Amirjalayer, Saeed; Woutersen, Sander

    2014-08-14

    Salt bridges are important interactions for the stability of protein conformations, but up to now it has been difficult to determine salt-bridge geometries in solution. Here we characterize the spatial structure of a salt bridge between guanidinium (Gdm(+)) and acetate (Ac(-)) using two-dimensional vibrational (2D-IR) spectroscopy. We find that as a result of salt bridge formation there is a significant change in the infrared response of Gdm(+) and Ac(-), and cross peaks between them appear in the 2D-IR spectrum. From the 2D-IR spectrum we determine the relative orientation of the transition-dipole moments of the vibrational modes of Gdm(+) and Ac(-), as well as the coupling between them. PMID:24676430

  12. Fluoride exposure of East African consumers using alkaline salt deposits known as magadi (trona) as a food preparation aid

    DEFF Research Database (Denmark)

    Nielsen, Joan Maj; Dahi, E.

    2002-01-01

    The fluoride content of Tanzanian and Kenyan magadi has been estimated to be in the range 0.1-17.9 mg F- g(-1), which is comparable with that reported elsewhere, but indicating a considerable variation in levels. The median fluoride content of crystalline magadi harvested from the alkaline lakes ...

  13. Investigation into formation of nanoparticles of tetravalent neptunium in slightly alkaline aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Husar, Richard

    2015-08-20

    Considering the worldwide growing discharge of minor actinides and the current need for geological disposal facilities for radioactive waste, this work provides a contribution to the safety case concerning Np transport if it would be released from deep repository sites and moving from alkaline cement conditions (near-field) to more neutral environmental conditions (far-field). The reducing conditions in a nuclear waste repository render neptunium tetravalent, which is assumed to be immobile in aqueous environment due to the low solubility solution of Np(IV). For tetravalent actinide nuclides, the most significant transport should occur via colloidal particles. This work demonstrates the formation of intrinsic neptunium dioxide nanocrystals and amorphous Np(IV) silica colloids under environmentally relevant conditions. The dissociation of the initial soluble Np(IV) complex (i.e. [Np(IV)(CO{sub 3}){sub 5}]{sup 6-}) induces the intrinsic formation of nanocrystalline NpO{sub 2} in the solution phase. The resulting irregularly shaped nanocrystals with an average size of 4 nm exhibit a face-centered cubic (fcc), fluorite-type structure (space group Fm anti 3m). The NCs tend to agglomerate under ambient conditions due to the weakly charged hydrodynamic surface at neutral pH (zetapotential ζ ∝0 mV). The formation of micron-sized agglomerates, composed of nanocrystals of 2-5 nm in size, and the subsequent precipitation cause immobilization of the major amount of Np(IV) in the Np carbonate system. Agglomeration of NpO{sub 2} nanocrystals in dependence on time was indicated by PCS and UV-vis absorption spectroscopy with the changes of baseline characteristics and absorption maximum at 742 nm. Hitherto, unknown polynuclear species as intermediate species of NpO{sub 2} nanocrystal formation were isolated from solution and observed by HR-TEM. These polynuclear Np species appear as dimers, trimers and hexanuclear compounds in analogy with those reported for other actinides

  14. Method of alkali solution concentration at electrochemical processing of eluates containing sodium salts

    OpenAIRE

    Трус, Інна Миколаївна; Гомеля, Микола Дмитрович; Радовенчик, Ярослав Вячеславович

    2013-01-01

    The paper gives the results of electrochemical concentration of alkali solutions, produced by electrolysis of sodium chloride or sodium sulfate. It was found that using two-chambered electrolyzer, the interelectrode space of which is separated by MK-40 membrane, allows increasing alkali concentration from 0.1-1.0D to 13D. It is shown that with anolyte alkalinity>0.1D alkali concentration in the anode region has little effect on electrolysis efficiency. Concentration is effective with alkal...

  15. Effects of applied potential on the stress corrosion cracking behavior of 7003 aluminum alloy in acid and alkaline chloride solutions

    Science.gov (United States)

    Zhang, Xiao-yan; Song, Ren-guo; Sun, Bin; Lu, Hai; Wang, Chao

    2016-07-01

    Potentiodynamic polarization tests and slow strain rate test (SSRT) in combination with fracture morphology observations were conducted to investigate the stress corrosion cracking (SCC) behavior of 7003 aluminum alloy (AA7003) in acid and alkaline chloride solutions under various applied potentials ( E a). The results show that AA7003 is to a certain extent susceptible to SCC via anodic dissolution (AD) at open-circuit potential (OCP) and is highly susceptible to hydrogen embrittlement (HE) at high negative E a in the solutions with pH levels of 4 and 11. The susceptibility increases with negative shift in the potential when E a is less than -1000 mV vs. SCE. However, the susceptibility distinctly decreases because of the inhibition of AD when E a is equal to -1000 mV vs. SCE. In addition, the SCC susceptibility of AA7003 in the acid chloride solution is higher than that in the alkaline solution at each potential. Moreover, the effect of hydrogen on SCC increases with increasing hydrogen ion concentration.

  16. Investigation into formation of nanoparticles of tetravalent neptunium in slightly alkaline aqueous solution

    International Nuclear Information System (INIS)

    Considering the worldwide growing discharge of minor actinides and the current need for geological disposal facilities for radioactive waste, this work provides a contribution to the safety case concerning Np transport if it would be released from deep repository sites and moving from alkaline cement conditions (near-field) to more neutral environmental conditions (far-field). The reducing conditions in a nuclear waste repository render neptunium tetravalent, which is assumed to be immobile in aqueous environment due to the low solubility solution of Np(IV). For tetravalent actinide nuclides, the most significant transport should occur via colloidal particles. This work demonstrates the formation of intrinsic neptunium dioxide nanocrystals and amorphous Np(IV) silica colloids under environmentally relevant conditions. The dissociation of the initial soluble Np(IV) complex (i.e. [Np(IV)(CO3)5]6-) induces the intrinsic formation of nanocrystalline NpO2 in the solution phase. The resulting irregularly shaped nanocrystals with an average size of 4 nm exhibit a face-centered cubic (fcc), fluorite-type structure (space group Fm anti 3m). The NCs tend to agglomerate under ambient conditions due to the weakly charged hydrodynamic surface at neutral pH (zetapotential ζ ∝0 mV). The formation of micron-sized agglomerates, composed of nanocrystals of 2-5 nm in size, and the subsequent precipitation cause immobilization of the major amount of Np(IV) in the Np carbonate system. Agglomeration of NpO2 nanocrystals in dependence on time was indicated by PCS and UV-vis absorption spectroscopy with the changes of baseline characteristics and absorption maximum at 742 nm. Hitherto, unknown polynuclear species as intermediate species of NpO2 nanocrystal formation were isolated from solution and observed by HR-TEM. These polynuclear Np species appear as dimers, trimers and hexanuclear compounds in analogy with those reported for other actinides. Intrinsic formation of NpO2 (fcc

  17. Study on Properties and Structural Parameters of Microemulsion CTAB/Butanol/Cyclohexane/Salt Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    Chen Yongjie; Qiu Guanming; Tian Yiguang; Fang Li; Xiao Linjiu; Sun Yanbin

    2005-01-01

    The phase diagrams of microemulsion CTAB/butanol/cyclohexane/aqueous solution of nitrate (or aqueous solution of ammonium salt) were determined and the structural parameters and ΔG*o→i were obtained by means of dilution method and theoretical calculation. The effect of different w/s and salt concentration on the stability and structural parameters of microemulsion were investigated. The result shows that with the increase of w/s, the area of microemulsion and Nd decrease, Rw, l and n increase; with the increase of salt concentration, the area of microemulsion, l and Nd decrease, ΔG*o→I, Rw and n increase. Theoretical basis of preparing size-controlled long afterglow luminescence materials and study of the relationship between fluorescence properties and particle size are provided.

  18. A new class of draw solutions for minimizing reverse salt flux to improve forward osmosis desalination.

    Science.gov (United States)

    Nguyen, Hau Thi; Nguyen, Nguyen Cong; Chen, Shiao-Shing; Ngo, Huu Hao; Guo, Wenshan; Li, Chi-Wang

    2015-12-15

    The applications of forward osmosis (FO) have been hindered because of the lack of an optimal draw solution. The reverse salt flux from the draw solution not only reduces the water flux but also increases the cost of draw solute replenishment. Therefore, in this study, Tergitol NP7 and NP9 with a long straight carbon chain and low critical micelle concentration (CMC) were coupled with highly charged ethylenediaminetetraacetic acid (EDTA) as an innovative draw solution to minimize reverse salt diffusion in FO for the first time. The results showed that the lowest reverse salt flux of 0.067 GMH was observed when 0.1M EDTA-2Na coupled with 15mM NP7 was used as a draw solution and deionized water was used as a feed solution in FO mode (active layer facing with the feed solution). This is due to the hydrophobic interaction between the tails of NP7 and the FO membrane, thus creating layers on the membrane surface and constricting the FO membrane pores. Moreover, 1M EDTA-2Na coupled with 15mM NP7 is promising as an optimal draw solution for brackish water and sea water desalination. Average water fluxes of 7.68, 6.78, and 5.95 LMH were achieved when brackish water was used as a feed solution (5, 10, and 20g/L NaCl), and an average water flux of 3.81 LMH was achieved when sea water was used as a feed solution (35g/L NaCl). The diluted draw solution was recovered using a nanofiltration (NF-TS80) membrane with a high efficiency of 95% because of the high charge and large size of the draw solution. PMID:26298255

  19. Electrosorption of inorganic salts from aqueous solution using carbon aerogels.

    Science.gov (United States)

    Gabelich, Christopher J; Tran, Tri D; Suffet, I H Mel

    2002-07-01

    Capacitive deionization (CDI) with carbon aerogels has been shown to remove various inorganic species from aqueous solutions, though no studies have shown the electrosorption behavior of multisolute systems in which ions compete for limited surface area. Several experiments were conducted to determine the ion removal capacity and selectivity of carbon aerogel electrodes, using both laboratory and natural waters. Although carbon aerogel electrodes have been treated as electrical double-layer capacitors, this study showed that ion sorption followed a Langmuir isotherm, indicating monolayer adsorption. The sorption capacity of carbon aerogel electrodes was approximately 1.0-2.0 x 10(-4) equiv/g aerogel, with ion selectivity being based on ionic hydrated radius. Monovalent ions (e.g., sodium) with smaller hydrated radii were preferentially removed from solution over multivalent ions (e.g., calcium) on a percent or molar basis. Because of the relatively small average pore size (4-9 nm) of the carbon aerogel material, only 14-42 m2/g aerogel surface area was available for ion sorption. Natural organic matter may foul the aerogel surface and limit CDI effectiveness in treating natural waters. PMID:12144279

  20. Salt Crystallization from an Evaporating Aqueous Solution by Molecular Dynamics Simulations

    Czech Academy of Sciences Publication Activity Database

    Mucha, Martin; Jungwirth, Pavel

    2003-01-01

    Roč. 107, č. 33 (2003), s. 8271-8274. ISSN 1089-5647 R&D Projects: GA MŠk LN00A032 Institutional research plan: CEZ:AV0Z4040901 Keywords : salt crystallization * aqueous solution * molecular dynamics Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.679, year: 2003

  1. Effect of salt solutions on the radiosensitivity of mammalian cells

    International Nuclear Information System (INIS)

    The effects of a wide concentration range of NaCl solutions containing either ouabain, ethanol, para-nitroacetophenone (PNAP), N-ethylmaleimide (NEM), cysteamine or dimethyl sulphoxide (DMSO) on cellular radiosensitivity have been examined. Ouabain and NEM treatment increased the radiosensitivity of V79 Chinese hamster cells, but the action of these chemicals did not depend on the concentration of NaCl. PNAP increased cellular radiosensitivity with increasing NaCl concentration reaching a maximum effect at 0.6 to 0.7 M NaCl. The radioprotective properties of cysteamine, DMSO and ethanol were all strongly dependent on the NaCl concentration in a complex but qualitatively similar manner. DMSO (2.0 M) increased survival of cells after a 1380 rad dose by a factor of about 104 when present in 0.075 NaCl and by a factor of 8.7 when present in 1.2 M NaCl. (author)

  2. Theoretical analysis of XANES for aqueous aluminum salt solutions

    Science.gov (United States)

    Matsuo, Shuji; Shirozu, Kaori; Tateishi, Yuichi; Wakita, Hisanobu; Yokoyama, Takushi

    In order to understand the coordination behavior of Al(III) ions in hydrosphere, discrete variational X[alpha] molecular orbital calculations were performed to analyze Al K-edge XANES spectra for the aqueous solutions of Al(NO3)3·9H2O and Al-EDTA (EDTA = ethylenediaminetetraacetate) complex. As to Al(NO3)3·9H2O, the hydrate structure was presumed to be rather an asymmetric hexahydrated structure than an high-symmetric structure. As to Al-EDTA, the 5-fold coordinated Al-EDTA was concluded to be the coexistence of the pyramidal and trigonal bipyramidal structures in proportion of 4 to 6.

  3. Investigation into the Formation of Nanoparticles of Tetravalent Neptunium in Slightly Alkaline Aqueous Solution

    OpenAIRE

    Husar, Richard

    2015-01-01

    Considering the worldwide growing discharge of minor actinides and the current need for geological disposal facilities for radioactive waste, this work provides a contribution to the safety case concerning Np transport if it would be released from deep repository sites and moving from alkaline cement conditions (near-field) to more neutral environmental conditions (far-field). The reducing conditions in a nuclear waste repository render neptunium tetravalent, which is assumed to be immobile i...

  4. Evidence for the Formation of Benzacridine Derivatives in Alkaline-Treated Sunflower Meal and Model Solutions

    Directory of Open Access Journals (Sweden)

    Verena Bongartz

    2016-01-01

    Full Text Available Sunflower extraction meal (SEM is an economically interesting protein source. During alkaline extraction of proteins, the presence of chlorogenic acid (CQA in the meal gives rise to the formation of o-quinones. Reactions with nucleophiles present in proteins can lead to green discoloration. Although such reactions have been known for a long time, there is a lack of information on the chemical nature of the reaction products. SEM and model systems consisting of amino acids and CQA were subjected to alkaline treatment and, for comparison, to oxidation of CQA by polyphenoloxidase (PPO. Several green trihydroxy benzacridine (TBA derivatives were tentatively identified in all samples by UHPLC-DAD-MS/MS. Surprisingly, in alkaline-treated samples of particular amino acids as well as in SEM, the same six TBA isomers were detected. In contrast, the enzymatically oxidized samples resulted in only three TBA derivatives. Contrary to previous findings, neither peptide nor amino acid residues were attached to the resultant benzacridine core. The results indicate that the formation of TBA derivatives is caused by the reaction between CQA quinones and free NH2 groups. Further research is necessary to elucidate the structure of the addition products for a comprehensive evaluation of food and feed safety aspects.

  5. Evidence for the Formation of Benzacridine Derivatives in Alkaline-Treated Sunflower Meal and Model Solutions.

    Science.gov (United States)

    Bongartz, Verena; Brandt, Lisa; Gehrmann, Mai Linh; Zimmermann, Benno F; Schulze-Kaysers, Nadine; Schieber, Andreas

    2016-01-01

    Sunflower extraction meal (SEM) is an economically interesting protein source. During alkaline extraction of proteins, the presence of chlorogenic acid (CQA) in the meal gives rise to the formation of o-quinones. Reactions with nucleophiles present in proteins can lead to green discoloration. Although such reactions have been known for a long time, there is a lack of information on the chemical nature of the reaction products. SEM and model systems consisting of amino acids and CQA were subjected to alkaline treatment and, for comparison, to oxidation of CQA by polyphenoloxidase (PPO). Several green trihydroxy benzacridine (TBA) derivatives were tentatively identified in all samples by UHPLC-DAD-MS/MS. Surprisingly, in alkaline-treated samples of particular amino acids as well as in SEM, the same six TBA isomers were detected. In contrast, the enzymatically oxidized samples resulted in only three TBA derivatives. Contrary to previous findings, neither peptide nor amino acid residues were attached to the resultant benzacridine core. The results indicate that the formation of TBA derivatives is caused by the reaction between CQA quinones and free NH2 groups. Further research is necessary to elucidate the structure of the addition products for a comprehensive evaluation of food and feed safety aspects. PMID:26784152

  6. Explicit-water theory for the salt-specific effects and Hofmeister series in protein solutions

    Science.gov (United States)

    Kalyuzhnyi, Yuriy V.; Vlachy, Vojko

    2016-06-01

    Effects of addition of salts on stability of aqueous protein solutions are studied theoretically and the results are compared with experimental data. In our approach, all the interacting species, proteins, ions, and water molecules, are accounted for explicitly. Water molecules are modeled as hard spheres with four off-center attractive square-well sites. These sites serve to bind either another water or to solvate the ions or protein charges. The ions are represented as charged hard spheres, and decorated by attractive sites to allow solvation. Spherical proteins simultaneously possess positive and negative groups, represented by charged hard spheres, attached to the surface of the protein. The attractive square-well sites, mimicking the protein-protein van der Waals interaction, are located on the surface of the protein. To obtain numerical results, we utilized the energy route of Wertheim's associative mean spherical approximation. From measurable properties, we choose to calculate the second virial coefficient B2, which is closely related to the tendency of proteins to aggregate and eventually crystalize. Calculations are in agreement with experimental trends: (i) For low concentration of added salt, the alkali halide salts follow the inverse Hofmeister series. (ii) At higher concentration of added salt, the trend is reversed. (iii) When cations are varied, the salts follow the direct Hofmeister series. (iv) In contrast to the colloidal theories, our approach correctly predicts the non-monotonic behavior of B2 upon addition of salts. (v) With respect to anions, the theory predicts for the B2 values to follow different sequences below and above the iso-ionic point, as also confirmed experimentally. (vi) A semi-quantitative agreement between measured and calculated values for the second virial coefficient, as functions of pH of solution and added salt type and concentration, is obtained.

  7. Modeling Solute Thermokinetics in LiCI-KCI Molten Salt for Nuclear Waste Separation

    Energy Technology Data Exchange (ETDEWEB)

    Morgan, Dane; Eapen, Jacob

    2013-10-01

    Recovery of actinides is an integral part of a closed nuclear fuel cycle. Pyrometallurgical nuclear fuel recycling processes have been developed in the past for recovering actinides from spent metallic and nitride fuels. The process is essentially to dissolve the spent fuel in a molten salt and then extract just the actinides for reuse in a reactor. Extraction is typically done through electrorefining, which involves electrochemical reduction of the dissolved actinides and plating onto a cathode. Knowledge of a number of basic thermokinetic properties of salts and salt-fuel mixtures is necessary for optimizing present and developing new approaches for pyrometallurgical waste processing. The properties of salt-fuel mixtures are presently being studied, but there are so many solutes and varying concentrations that direct experimental investigation is prohibitively time consuming and expensive (particularly for radioactive elements like Pu). Therefore, there is a need to reduce the number of required experiments through modeling of salt and salt-fuel mixture properties. This project will develop first-principles-based molecular modeling and simulation approaches to predict fundamental thermokinetic properties of dissolved actinides and fission products in molten salts. The focus of the proposed work is on property changes with higher concentrations (up to 5 mol%) of dissolved fuel components, where there is still very limited experimental data. The properties predicted with the modeling will be density, which is used to assess the amount of dissolved material in the salt; diffusion coefficients, which can control rates of material transport during separation; and solute activity, which determines total solubility and reduction potentials used during electrorefining. The work will focus on La, Sr, and U, which are chosen to include the important distinct categories of lanthanides, alkali earths, and actinides, respectively. Studies will be performed using LiCl-KCl salt

  8. Solution behavior and activity of a halophilic esterase under high salt concentration.

    Directory of Open Access Journals (Sweden)

    Lang Rao

    Full Text Available BACKGROUND: Halophiles are extremophiles that thrive in environments with very high concentrations of salt. Although the salt reliance and physiology of these extremophiles have been widely investigated, the molecular working mechanisms of their enzymes under salty conditions have been little explored. METHODOLOGY/PRINCIPAL FINDINGS: A halophilic esterolytic enzyme LipC derived from archeaon Haloarcula marismortui was overexpressed from Escherichia coli BL21. The purified enzyme showed a range of hydrolytic activity towards the substrates of p-nitrophenyl esters with different alkyl chains (n = 2-16, with the highest activity being observed for p-nitrophenyl acetate, consistent with the basic character of an esterase. The optimal esterase activities were found to be at pH 9.5 and [NaCl] = 3.4 M or [KCl] = 3.0 M and at around 45 degrees C. Interestingly, the hydrolysis activity showed a clear reversibility against changes in salt concentration. At the ambient temperature of 22 degrees C, enzyme systems working under the optimal salt concentrations were very stable against time. Increase in temperature increased the activity but reduced its stability. Circular dichroism (CD, dynamic light scattering (DLS and small angle neutron scattering (SANS were deployed to determine the physical states of LipC in solution. As the salt concentration increased, DLS revealed substantial increase in aggregate sizes, but CD measurements revealed the maximal retention of the alpha-helical structure at the salt concentration matching the optimal activity. These observations were supported by SANS analysis that revealed the highest proportion of unimers and dimers around the optimal salt concentration, although the coexistent larger aggregates showed a trend of increasing size with salt concentration, consistent with the DLS data. CONCLUSIONS/SIGNIFICANCE: The solution alpha-helical structure and activity relation also matched the highest proportion of enzyme unimers

  9. Process and system for reducing the inactive salt concentration in waste solutions of nuclear power plants

    International Nuclear Information System (INIS)

    The method is based on a suitable combination of most modern separation measures as there are precipitation, filtration, ultra-filtration, reverse osmosis, ion exchange, evaporation and crystallization; in this method almost the total quantity of the components with radioactivity, except tritium, can be effectively separated from inactive salts. One part of the inactive salt (alkali nitrate) can be treated as industrial waste and the other part (boric acid) can be recycled. The method of the invention as well as the equipment used for its execution can considerably reduce the high costs of waste solution treatment in nuclear power stations. (orig./RB)

  10. Investigation of the Ionic Hydration in Aqueous Salt Solutions by Soft X-ray Emission Spectroscopy.

    Science.gov (United States)

    Jeyachandran, Y L; Meyer, F; Benkert, A; Bär, M; Blum, M; Yang, W; Reinert, F; Heske, C; Weinhardt, L; Zharnikov, M

    2016-08-11

    Understanding the molecular structure of the hydration shells and their impact on the hydrogen bond (HB) network of water in aqueous salt solutions is a fundamentally important and technically relevant question. In the present work, such hydration effects were studied for a series of representative salt solutions (NaCl, KCl, CaCl2, MgCl2, and KBr) by soft X-ray emission spectroscopy (XES) and resonant inelastic soft X-ray scattering (RIXS). The oxygen K-edge XES spectra could be described with three components, attributed to initial state HB configurations in pure water, water molecules that have undergone an ultrafast dissociation initiated by the X-ray excitation, and water molecules in contact with salt ions. The behavior of the individual components, as well as the spectral shape of the latter component, has been analyzed in detail. In view of the role of ions in such effects as protein denaturation (i.e., the Hofmeister series), we discuss the ion-specific nature of the hydration shells and find that the results point to a predominant role of anions as compared to cations. Furthermore, we observe a concentration-dependent suppression of ultrafast dissociation in all salt solutions, associated with a significant distortion of intact HB configurations of water molecules facilitating such a dissociation. PMID:27442708

  11. Thermophysical property characterization of aqueous amino acid salt solutions containing α-aminobutyric acid

    International Nuclear Information System (INIS)

    Highlights: • Thermophysical properties of aqueous potassium and sodium salt solutions of α-aminobutyric acid were studied. • Density, electrolytic conductivity, refractive index, and viscosity of the solution were measured. • The concentrations of amino acid salt ranges from x1 = 0.009 to 0.06. • The temperature range studied was (303.15 to 343.15) K. • The measured data were represented satisfactorily by using the applied correlations. - Abstract: In this study, density, electrical conductivity, refractive index and viscosity of aqueous potassium and sodium salt solutions of α-aminobutyric acid were presented. Measurements were done over the temperature range (303.15 to 343.15) K and atmospheric pressure for salt compositions from x1 = 0.009 to 0.062. A modified Graber et al. equation was used to correlate the density, electrical conductivity, and refractive index with temperature and composition leading to average absolute deviations (AAD) between the predicted and calculated values of 0.04%, 0.7%, and 0.01%, respectively. The viscosity data were represented as a function of temperature and composition via Vogel–Tamman–Fulcher (VTF) type equation at an AAD of 0.6%

  12. Changes in Soil Solution Cu and Zn Follogwing Application of Alkaline Stabilised Sewage Sludge and Gamma-Irradiation

    Institute of Scientific and Technical Information of China (English)

    1998-01-01

    A glasshouse pot experiment was conducted to study study changes in the solubility of copper and zinc in the soil-plant system follwing heavy application of sewage sludge and partial sterilisation of the sludge/soil mixture,A silghtly acid sandy loam was mixed with alkaline stabilised and composted urban sewage sludge solids ('Agri-Soil',180 t hm-2),and the soil/sludge mixture was γ-irradiated( 10 kGy).The contrasts without the application of sewage sludge and γ-irradiation were also included in the experiment.Perennial ryegrass(Lolium perenne,cv.Magella) was grown on irradiated and unirradiated soils for 50 days. Soil solution samples were obtained using soil suction samplers immediately before plant transplantation and every ten days thereafter.The soil solution smmples were used directly for determination of Cu and Zn,together with pH,electrical conductivity(EC) and absorbance at wavelength 360 nm(A360).Application of Agri-Soil led to a substantial increase in dissolved Cu and a significant derease in dissolved Zn in the soil solution and thess effect were accompanied by increased soil solution pH ,EC and A360 ,The alkaline sludge product(Agri-Soil) in combination with γ-irradiation also led to pronounced elevtion of Cu and A360 but a marked decline in EC, indicatig an increase in dissolvedorganic compounds and a decrease in the ionic strength of the soil solution ,The dissolved Cu and Zn,EC and A360 usually decreased while the ph increased fter plant growth for 50 days.

  13. Removal of uranium, plutonium and americum particles from alkaline colloidal solution by froth flotation

    International Nuclear Information System (INIS)

    Fine particulate oxides of actinide elements can be separated from other oxidized material - in particular, Mg(OH)2 -by froth flotation in slightly alkaline media. The flotation medium contains sodium bicarbonate and the frother, a cationic surfactant such as cetyl trimethyl ammonium bromide. A series of small batch flotation tests used to characterize the process is described. In a typical good run, 99% of the uranium can be removed in 30% of the initial water. About 25% of the Mg(OH)2 is recovered in the same type of experiment. (author)

  14. Contribution to the study of uranyl salts in butyl phosphate solutions

    International Nuclear Information System (INIS)

    A spectroscopic study in the normal infrared region and involving the following associations: tri-alkyl phosphates (tri-butyl, tri-ethyl, tri-methyl), uranyl salts (nitrate, chloride, acetate) has confirmed the existence of an interaction between the phosphoryl group and the uranium atom, as shown by a movement of absorption band for the valency P = 0 from ∼ 1270 cm-1 to ∼ 1180 cm-1. A study of the preparation, analysis and spectroscopy of the solids obtained by the precipitation of uranyl salts by acid butyl phosphates has been carried out. By infrared spectrophotometry it has been shown that the tri-butyl and di-butyl phosphates are associated in non-polar diluents even before the uranium is introduced. The extraction of uranyl salts from acid aqueous solutions by a diluted mixture of tri-butyl and di-butyl phosphates proceeds by different mechanisms according to the nature of the ion (nitrate or chloride). (author)

  15. Modeling of Dielectric Properties of Aqueous Salt Solutions with an Equation of State

    DEFF Research Database (Denmark)

    Maribo-Mogensen, Bjørn; Kontogeorgis, Georgios; Thomsen, Kaj

    2013-01-01

    , been ignored in relation to thermodynamic modeling, and authors have either neglected the effect of salts on permittivity or used empirical correlations fitted to the measured static permittivity, leading to an overestimation of the reduction in the thermodynamic static permittivity. We present a new...... in the electrical field surrounding ions. Kinetic depolarization may explain 25–75% of the observed decrease in the permittivity of solutions containing salts, but since this is a dynamic property, this effect should not be included in the thermodynamic modeling of electrolytes. Kinetic depolarization has, however...... methodology for obtaining the static permittivity over wide ranges of temperatures, pressures, and compositions for use within an equation of state for mixed solvents containing salts. The static permittivity is calculated from a new extension of the framework developed by Onsager, Kirkwood, and Fröhlich...

  16. Study of the alloying additives and alkaline zincate solution effects on the commercial aluminum as galvanic anode for use in alkaline batteries

    International Nuclear Information System (INIS)

    The corrosion behavior of different grades of commercial aluminum such as AA1040, AA5083, AA6060 and AA7075 in ZnO-containing 4 M NaOH has been determined by using open circuit potential-time measurements (OCP), galvanostatic and potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results of scanning electron microscopy (SEM) and energy dispersive analysis of X-ray (EDAX) reveal that ZnO produces the inhibition effect by the formation of a zinc-containing deposit layer on the surface of aluminum electrodes. Although the influence of zincating on the performance of aluminum alloys and considering the amount of alloying elements such as zinc, magnesium and manganese in AA7075 and AA5083 alloys is much more than AA6060 one, the AA6060 aluminum exhibits negligible corrosion rate. Alloying aluminum with other elements and modifying the composition of the electrolyte is a necessary condition for reducing the self-corrosion of the aluminum anodes, whereas the proportion of the amount of additive elements is sufficient and important condition. As AA6060 with a low amount of Zn and Mg, but the high value of the ratio of (Mg/Zn) content (>400) can serve as a good galvanic anode in the alkaline media. - Highlights: • Decreasing the corrosion rate of tested alloys in 4 M NaOH solution specially AA6060. • Lowering the extent of anodic polarization at a current density of 50 mA cm−2. • High inhibitor efficiency about 97% for AA6060

  17. Study of the alloying additives and alkaline zincate solution effects on the commercial aluminum as galvanic anode for use in alkaline batteries

    Energy Technology Data Exchange (ETDEWEB)

    Rashvand avei, M. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of); Jafarian, M., E-mail: mjafarian@kntu.ac.ir [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of); Moghanni Bavil Olyaei, H. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of); Gobal, F. [Department of Chemistry, Sharif University of Technology, P.O. Box 11365-8516, Tehran (Iran, Islamic Republic of); Hosseini, S.M. [Jahad Organization – Science and Technology Center, Tehran (Iran, Islamic Republic of); Mahjani, M.G. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of)

    2013-12-16

    The corrosion behavior of different grades of commercial aluminum such as AA1040, AA5083, AA6060 and AA7075 in ZnO-containing 4 M NaOH has been determined by using open circuit potential-time measurements (OCP), galvanostatic and potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results of scanning electron microscopy (SEM) and energy dispersive analysis of X-ray (EDAX) reveal that ZnO produces the inhibition effect by the formation of a zinc-containing deposit layer on the surface of aluminum electrodes. Although the influence of zincating on the performance of aluminum alloys and considering the amount of alloying elements such as zinc, magnesium and manganese in AA7075 and AA5083 alloys is much more than AA6060 one, the AA6060 aluminum exhibits negligible corrosion rate. Alloying aluminum with other elements and modifying the composition of the electrolyte is a necessary condition for reducing the self-corrosion of the aluminum anodes, whereas the proportion of the amount of additive elements is sufficient and important condition. As AA6060 with a low amount of Zn and Mg, but the high value of the ratio of (Mg/Zn) content (>400) can serve as a good galvanic anode in the alkaline media. - Highlights: • Decreasing the corrosion rate of tested alloys in 4 M NaOH solution specially AA6060. • Lowering the extent of anodic polarization at a current density of 50 mA cm{sup −2}. • High inhibitor efficiency about 97% for AA6060.

  18. Cysteine as a green corrosion inhibitor for Cu37Zn brass in neutral and weakly alkaline sulphate solutions.

    Science.gov (United States)

    Radovanović, Milan B; Petrović, Marija B; Simonović, Ana T; Milić, Snežana M; Antonijević, Milan M

    2013-07-01

    The aim of this study was to investigate electrochemical properties of brass in neutral and weakly alkaline solutions in the presence of cysteine as a nontoxic and ecological corrosion inhibitor. Potentiodynamic measurements, open circuit potential measurements, as well as chronoamperometric measurements were the methods used during investigation of the inhibitory effect of cysteine on the corrosion behaviour of brass. Potentiodynamic measurements showed that cysteine behaves as a mixed-type inhibitor in the investigated media. Based on polarization curves for brass in a weakly alkaline solution of sodium sulphate at varying cysteine concentrations, an interaction occurs between Cu(+) ions and the inhibitor, resulting in the formation of a protective complex on the electrode surface. The results of chronoamperometric measurements confirm the results obtained by potentiodynamic measurements. Optical microphotography of the brass surface also confirms the formation of a protective film in the presence of a 1 × 10(-4) mol/dm(3) cysteine. Adsorption of cysteine on the brass surface proceeds according to the Langmuir adsorption isotherm. PMID:22836675

  19. The affects of membrane on the cell performance when using alkaline borohydride-hydrazine solutions as the fuel

    Energy Technology Data Exchange (ETDEWEB)

    Qin, Haiying; Liu, Zixuan; Guo, Yanfeng; Li, Zhoupeng [Department of Chemical and Bio-chemical Engineering, Zhejiang University, Hangzhou 310027 (China)

    2010-04-15

    The cell performance and the polarization behavior of the fuel cell using alkaline NaBH{sub 4}-N{sub 2}H{sub 4} solutions as the fuel were investigated. It was found that the use of different membrane: anion exchange membrane (AEM) or cation exchange membrane (CEM) would influence the cell performance and cathode polarization behavior. The direct borohydride fuel cell (DBFC) using CEM gave a higher power density than that using AEM, but the direct hydrazine fuel cell (DHFC) using CEM gave a lower power density compared with the DHFC using AEM. In the DBFCs using CEM, N{sub 2}H{sub 4} addition in alkaline NaBH{sub 4} solution improved the cell performance but it did not make any difference when adding more N{sub 2}H{sub 4}. On the other hand, in the DBFCs using AEM, cell performance was improved with increasing the amount of N{sub 2}H{sub 4} in the anolyte. (author)

  20. Inorganic polymers from laterite using activation with phosphoric acid and alkaline sodium silicate solution: Mechanical and microstructural properties

    Energy Technology Data Exchange (ETDEWEB)

    Lassinantti Gualtieri, Magdalena, E-mail: magdalena.gualtieri@unimore.it [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Romagnoli, Marcello [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Pollastri, Simone; Gualtieri, Alessandro F. [Dipartimento di Scienze Chimiche e Geologiche, Università degli studi di Modena e Reggio Emilia, Via S. Eufemia 19I, I-41121 Modena (Italy)

    2015-01-15

    Geopolymers from laterite, an iron-rich soil available in developing countries, have great potential as building materials. In this work, laterite from Togo (Africa) was used to prepare geopolymers using both phosphoric acid and alkaline sodium silicate solution. Microstructural properties were investigated by scanning electron microscopy, X-ray powder diffraction and mercury porosimetry, whereas thermal properties were evaluated by thermal analyses. The local environment of iron was studied by X-ray Absorption Spectroscopy (XANES region). The mechanical properties were determined. Modulus of Rupture and Young's modulus fell in the ranges 3.3–4.5 MPa and 12–33 GPa, respectively, rendering the materials good candidates for construction purposes. Heating above 900 °C results in weight-gain, presumably due to iron redox reactions. X-ray Absorption Spectroscopy data evidence changes in the chemical and structural environments of iron following thermal treatment of geopolymers. These changes indicate interaction between the geopolymer structure and iron during heating, possibly leading to redox properties. -- Highlights: •Geopolymerization of laterite is promising for fabrication of building materials. •Both phosphoric acid and alkaline sodium silicate solution can be used for activation. •Thermally activated redox properties of the inorganic polymers were observed.

  1. Inorganic polymers from laterite using activation with phosphoric acid and alkaline sodium silicate solution: Mechanical and microstructural properties

    International Nuclear Information System (INIS)

    Geopolymers from laterite, an iron-rich soil available in developing countries, have great potential as building materials. In this work, laterite from Togo (Africa) was used to prepare geopolymers using both phosphoric acid and alkaline sodium silicate solution. Microstructural properties were investigated by scanning electron microscopy, X-ray powder diffraction and mercury porosimetry, whereas thermal properties were evaluated by thermal analyses. The local environment of iron was studied by X-ray Absorption Spectroscopy (XANES region). The mechanical properties were determined. Modulus of Rupture and Young's modulus fell in the ranges 3.3–4.5 MPa and 12–33 GPa, respectively, rendering the materials good candidates for construction purposes. Heating above 900 °C results in weight-gain, presumably due to iron redox reactions. X-ray Absorption Spectroscopy data evidence changes in the chemical and structural environments of iron following thermal treatment of geopolymers. These changes indicate interaction between the geopolymer structure and iron during heating, possibly leading to redox properties. -- Highlights: •Geopolymerization of laterite is promising for fabrication of building materials. •Both phosphoric acid and alkaline sodium silicate solution can be used for activation. •Thermally activated redox properties of the inorganic polymers were observed

  2. Phase equilibrium of methane hydrate in silica sand containing chloride salt solution

    International Nuclear Information System (INIS)

    Highlights: • Methane hydrate equilibria in silica sand-ionic solution are obtained. • Hydrate equilibria in fine sand-solution shift more than single sand or solution. • Electrostatic and capillary forces affect hydrate equilibria in fine sand-solution. • Hydrate equilibria in coarse sand-solution agree with those in single solution. • Hydrate equilibria in coarse sand-solution are mainly affected by ions. - Abstract: Hydrate equilibrium is the most important foundation for other hydrate issues, especially for marine environment condition. In this work, the silica sand containing NaCl/MgCl2/CaCl2 aqueous solution were used to simulate marine sediment for investigating methane hydrate equilibrium using isochoric multi-step heating dissociation method. All measurements were performed in a temperature and pressure range of (279.5 to 289.7) K and (8.32 to 17.52) MPa, respectively. The results suggest that the equilibrium of methane hydrate in fine-grained silica sand containing chloride salt solution shifts more greatly to the left relative to that in single silica sand or solution. This is because water molecules reduce more chances to combine with gas molecules that is caused by the capillary force and the electrostatic attractions from the surface and electrolyte ions. However, hydrate equilibrium in coarse-grained silica sand containing chloride salt solution is in rough agreement with that in ionic solution of the corresponding concentration that indicates that hydrate equilibrium is mainly influenced by ions while the impact of solid particles is negligible

  3. Adsorption of alkali and alkaline earth radionuclides on zeolite from water solutions

    International Nuclear Information System (INIS)

    The adsorption of cesium and strontium ions from water solutions on zeolite has been investigated in presence of sodium, potassium, magnesium and calcium ions. Distribution ratios of cesium and strontium on the zeolite were determined in solutions of various compositions and solution volume to sorbent weight ratios (batch factor). Breakthrough curves for zeolite layers are reported. (author) 7 refs.; 4 figs

  4. Nicotine aqueous solutions: pH-measurements and salting-out effects - analysis of the effective Gibbs energies of hydration and ionic strengths of the solutions

    Directory of Open Access Journals (Sweden)

    Grozdanić Nikola D.

    2014-01-01

    Full Text Available This work is a continuation of our previous studies on the phase demixing - salting-out effects - in aqueous nicotine solutions. Thus, pH measurements were carried out allowing a brief analysis of the existing hydrogen bond interactions. Salting-out effects - the related experimental cloud point shifts - provoked by the addition of two inorganic salts, potassium nitrate and sodium sulfate, which were not studied so far, were determined. Analysis of the current and our previously reported salting-out/or salting-in phenomena in nicotine aqueous solutions was performed. In this respect, five studied salts were included: four inorganic salts (sodium chloride, potassium nitrate, sodium sulfate and sodium phosphate (Na3PO4 and ionic liquid 1-ethyl-3-methylimidazolium ethyl sulfate ([C2mim][EtSO4] or ECOENG212®. Based on the pH measurements the effective Gibbs energies of hydration and ionic strengths of the respective ternary solutions were calculated and plotted against the related cloud-point shifts caused by the addition of the salts. For the studied salts, the results and diagram obtained within this work may be used to predict the cloud-points shifts, based on the related quantities of the salts added and/or the molar Gibbs energies of hydration and/or ionic strengths requested in each case. [Projekat Ministarstva nauke Republike Srbije, br. 172063

  5. Synthesis and infrared spectra of alkaline earth metal carbonates formed by the reaction of metal salts with urea at high temperature

    Indian Academy of Sciences (India)

    S M Teleb; D El-Sayed Nassr; E M Nour

    2004-12-01

    The metal carbonate, MCO3 (M = Ca, Sr and Ba), was synthesized by a novel method of reacting aqueous solution of each of Ca2+, Sr2+ and Ba2+ salts with urea at high temperature, ∼ 80°C. The reaction products were characterized through elemental analysis and infrared spectra. The infrared spectra of the products are the same as those of the corresponding commercially obtained carbonates. A general reaction describing the formation of MCO3 is proposed.

  6. Determination of γ-spectrometric parameters for some chloride salt solutions

    International Nuclear Information System (INIS)

    The mass attenuation coefficients, atomic cross-sections and effective atomic numbers are determined for LiCl, NaCl and KCl solutions with contents up to 0.2 g cm-3.The energies used are 0.511, 0.662 and 1.274 keV. The combined results were employed to determine the mass attenuation coefficients and atomic cross-sections of the salts and water in the solutions. The results are compared with the calculated values from elemental data. It was found that the mass attenuation coefficients and corresponding total cross-sections are, in general, less from measurement than from tabulated data, either for water or for the chloride salts

  7. The nonmetal-metal transition in solutions of metals in molten salts

    International Nuclear Information System (INIS)

    Solutions of metals in molten salts present a rich phenomenology: localization of electrons in disordered ionic media, activated electron transport increasing with metal concentration towards a nonmetal-metal (NM-M) transition, and liquid-liquid phase separation. A brief review of progress in the study of these systems is given in this article, with main focus on the NM-M transition. After recalling the known NM-M behaviour of the component elements in the case of expanded fluid alkali metals and mercury and of solid halogens under pressure, the article focuses on liquid metal - molten salt solutions and traces the different NM-M behaviours of the alkalis in their halides and of metals added to polyvalent metal halides. (author). 51 refs, 2 figs

  8. Aminoguanidinium closo-borates and their reactions with copper(2) salts in aqueous solutions

    International Nuclear Information System (INIS)

    Amino guanidine hexa-, deca- and dodecaborates of the (AguH)2BnHn · xH2O, where Agu - (CN4H6); n = 6, 10, 12; x = 1, 2, composition were synthesized and defined by means of element, magnetic susceptibility and IR spectroscopy analyses. Their reaction with the copper(2) salts in aqueous solutions was studied. It was shown that cation-anion interaction, which was enhanced in the B12 10 6 row, were the case in the amino guanidine closo-borates. The reaction of the amino guanidine closo-borates with the copper(2) salts in aqueous solutions leads to formation either complexes (n = 10, 12) or elemental copper (in the case of B6H62- anion) depending on closo-borate anion BnHn2-

  9. Stoichiometric C6-oxidation of hyaluronic acid by oxoammonium salt TEMPO⁺Cl⁻ in an aqueous alkaline medium.

    Science.gov (United States)

    Ponedel'kina, Irina Yu; Khaibrakhmanova, Elvira A; Tyumkina, Tatyana V; Romadova, Irina V; Odinokov, Victor N

    2015-10-01

    This paper reports the selective oxidation of hyaluronic acid (HA) by stoichiometric quantity of 2,2,6,6-tetramethylpiperidine-1-oxoammonium chloride (TEMPO(+)) in aqueous alkaline medium. High efficiency of the HA oxidation and quantitative yield of carboxy-HA per starting TEMPO(+), as well as unusual behavior of the oxidation system generating an oxygen upon alkali-induced oxoammonium chloride decomposition are demonstrated. The scheme for HA oxidation involving both TEMPO(+) and oxygen produced upon the TEMPO(+)Cl(-) decomposition and/or air oxygen is proposed. For comparison, the data on stoichiometric oxidation of such substrates as dermatan sulfate, water-soluble potato starch, methyl 2-acetamido-2-deoxy-β-d-glucopyranoside and ethanol are presented. PMID:26076602

  10. Titanium Nitride Nanoparticle Electrocatalysts for Oxygen Reduction Reaction in Alkaline Solution

    KAUST Repository

    Ohnishi, R.

    2013-03-12

    Monodispersed TiN nanoparticles with a narrow size distribution (7–23 nm) were synthesized using mesoporous graphitic (mpg)-C3N4 templates with different pore sizes. The nano-materials were examined as electrocatalysts for oxygen reduction reaction (ORR) in alkaline media. The TiN nanoparticles were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), N2 sorption, transmission electron microscopy (TEM), and C-H-N elemental analysis. The ORR current increased as the TiN particle size decreased, and hence the surface area of TiN nanoparticles reactive to ORR increased. Rotating ring disk electrode (RRDE) measurements revealed that the ORR on TiN surfaces proceeded mainly via a two-electron pathway, producing H2O2 as the main product. Mechanistic aspects of ORR on TiN surfaces are discussed.

  11. Anodic behavior of stainless-steel substrate in organic electrolyte solutions containing different lithium salts

    International Nuclear Information System (INIS)

    Highlights: • We investigated anodic behavior of stainless-steel in organic electrolytes for advanced capacitor. • Anion of the electrolyte affected the anodic stability of the alloy. • Anodic passivation occurs in LiPF6 solution but pitting or active dissolution proceeds in other electrolyte solutions. • Fluoride source in the solution contributes to forming a stable surface layer on the stainless steel. - Abstract: The anodic behavior of austenitic stainless-steel, SUS304, as a current collector of positive electrode in lithium-ion battery/capacitor has been investigated in organic electrolyte solutions based on a mixed alkyl carbonate solvent with different lithium salts. Stable passivation characteristics were observed for the stainless-steel in the LiPF6 solution, but pitting corrosion or active dissolution proceeded in the solutions containing other anions, BF4-, (CF3SO2)2N- (TFSA-) and ClO4-. The mass ratios of the dissolved metal species in the solutions of LiTFSA and LiClO4 were equivalent to that of the alloy composition, which suggests that no preferential dissolution occurs during the anodic polarization in these electrolyte solutions. An HF component formed by decomposition of PF6- with the contaminate water will act as an F- source for the formation of a surface fluoride layer, that will contribute to the anodic stability of SUS304 in the LiPF6 solution. The anodic corrosion in the LiTFSA solution was suppressed in part by mixing the PF6 salt or adding HF in the electrolyte

  12. Anions of alkali halide salts at surfaces of formamide solutions: Concentration depth profiles and surface topography

    Czech Academy of Sciences Publication Activity Database

    Andersson, G.; Morgner, H.; Cwiklik, Lukasz; Jungwirth, Pavel

    2007-01-01

    Roč. 111, č. 11 (2007), s. 4379-4387. ISSN 1932-7447 R&D Projects: GA MŠk LC512; GA MŠk ME 644 Grant ostatní: DFG(DE) 288/25 Institutional research plan: CEZ:AV0Z40550506 Keywords : surfaces of salt solutions * formamide * ions * molecular dynamics simulations Subject RIV: CF - Physical ; Theoretical Chemistry

  13. Alkaline battery, separator therefore

    Science.gov (United States)

    Schmidt, George F. (Inventor)

    1980-01-01

    An improved battery separator for alkaline battery cells has low resistance to electrolyte ion transfer and high resistance to electrode ion transfer. The separator is formed by applying an improved coating to an electrolyte absorber. The absorber, preferably, is a flexible, fibrous, and porous substrate that is resistant to strong alkali and oxidation. The coating composition includes an admixture of a polymeric binder, a hydrolyzable polymeric ester and inert fillers. The coating composition is substantially free of reactive fillers and plasticizers commonly employed as porosity promoting agents in separator coatings. When the separator is immersed in electrolyte, the polymeric ester of the film coating reacts with the electrolyte forming a salt and an alcohol. The alcohol goes into solution with the electrolyte while the salt imbibes electrolyte into the coating composition. When the salt is formed, it expands the polymeric chains of the binder to provide a film coating substantially permeable to electrolyte ion transfer but relatively impermeable to electrode ion transfer during use.

  14. Inefficacy of osmotic backwash induced by sodium chloride salt solution in controlling SWRO membrane fouling

    Science.gov (United States)

    Farooque, A. Mohammed; Al-Jeshi, Subhi; Saeed, Mohamed O.; Alreweli, Ali

    2014-12-01

    A study was conducted to evaluate the efficacy of osmotic backwash induced by high salt (NaCl) concentration solution on feed side of seawater reverse osmosis (SWRO) membranes, online and offline, in controlling membrane fouling and therefore minimizing/eliminating the need for chemical cleaning. SWRO membranes were deliberately fouled by feeding seawater from an open intake located on the Arabian Gulf Coast without dosing chemicals. The fouled membranes were subjected to offline cleaning with the salt solution of up to 25 % concentration. Despite the partial removal of foulants from the membrane surface, SWRO membrane performance could not be restored, indicating the ineffectiveness of osmotic backwash in aiding offline salt cleaning. Similarly, online osmotic backwash was found to be not only ineffective in removing foulants from membrane surfaces but actually increased the fouling rate, as indicated by faster fouling rates compared to other cases. Although the driving force required for the osmotic backwash existed, the generated back flow proved to be insufficient to detach foulants from membrane surfaces. During the study period, the average SWRO membrane flux was maintained between 19 and 23 LMH, whereas the average generated back flow flux by high salt concentration solution was only 11 LMH, which was not adequate to remove foulants from membrane surfaces. Moreover, it seems that the membrane configuration as well as inherent microstructure of SWRO membrane places certain constraints on the osmotic backwash process and renders osmotic backwash ineffective in tackling SWRO membrane fouling. Hence, chemical cleaning is essential to restore SWRO membrane performance whenever fouling occurs, and the use of highly concentrated salt solution does not have any significant benefit. Membrane autopsy revealed only an insignificant accumulation of biofouling layer despite the absence of disinfection. However, it was shown that culturable biofilm bacteria species

  15. The Chemistry and Thermodynamics of Molten-Salt-Reactor Fluoride Solutions

    International Nuclear Information System (INIS)

    A solvent of lithium and beryllium fluorides (about 2 moles of LiF per mole of BeF2) is used in the fuel salt, the coolant salt, and the flush salt of the Molten Salt Reactor Experiment. As a result of the chemical development work done for this reactor concept, considerable chemical and thermodynamic information has been acquired concerning this solvent and its solutions with actinide, lanthanide, and structural metal fluorides. It is the purpose of this paper to review this information, much of which is not yet generally available. The data were obtained mainly by measurements of heterogeneous equilibria, i.e. by equilibration of melts with gaseous mixtures containing hydrogen, hydrogen fluoride or water and by determinations of solid-liquid phase equilibria. The results of these measurements gave direct information about such important chemical problems as: (1) the corrodibility of structural metals and the reducibility of the structural metal ions, Ni2+, Fe2+, Cr2+; (2) reactions with water vapour to form oxide and hydroxide ions, and the removal of these ions; (3) the precipitation, solubility, and tendency toward solid-solution formation of the oxides of beryllium, uranium, zirconium, thorium and the rare earths; (4) the stability of uranium(IV) toward reduction to the trivalent state and possible subsequent disproportionation; and (5) the solubilities and solid solution formation of rare earth fluorides. Equally important has been the wider usefulness of this information when the methods of thermodynamics are brought to bear. Thus the data obtained could be used to: (1) correlate, revise, and extend existing thermochemical data on fluorides and oxides; (2) determine activity coefficients of the components LiF, BeF2, UF4 , ZrF4, and NiF2 in these molten salt solutions; (3) revise the generally accepted phase diagram for UO2-ZrO2; and (4) estimate solubilities and reactivities of compounds not directly investigated. Thus the chemical development programme for

  16. Modified multi-walled carbon nanotube/Ag nanoparticle composite catalyst for the oxygen reduction reaction in alkaline solution

    International Nuclear Information System (INIS)

    Highlights: • Ag/m-MWCNT catalyst is prepared by a facile in situ growth method. • Ag nanoparticles with a mean diameter of 10.6 nm are anchored to the surfaces of m-MWCNTs. • Ag/m-MWCNT catalyst shows high electrocatalytic activity for ORR in alkaline solution. -- Abstract: The modified multi-walled carbon nanotubes (m-MWCNTs)/Ag composite catalyst (Ag/m-MWCNTs) is prepared successfully by a facile in situ growth method. The physicochemical properties of Ag/m-MWCNTs are characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and electrochemical measurements. The results demonstrate that the dispersed Ag nanoparticles are anchored on the surface of m-MWCNTs with a mean diameter about 10.6 nm. The as-prepared Ag/m-MWCNTs catalyst shows high electrocatalytic activity toward the oxygen reduction reaction (ORR) in alkaline media. The ORR is dominated by four-electron pathway in the limiting diffusion zone, which is similar to the commercial Pt/C catalyst. The high catalytic activity of the Ag/m-MWCNTs can ascribe to the dispersed Ag nanoparticles on the m-MWCNTs which not only facilitate the ORR process, but also may promote the decomposition or further reduction of HO2− formed at the surfaces of the MWCNTs

  17. Reductive atmospheric acid leaching of spent alkaline batteries in H2SO4/Na2SO3 solutions

    Science.gov (United States)

    Morcali, Mehmet Hakan

    2015-07-01

    This work studies the optimum reductive leaching process for manganese and zinc recovery from spent alkaline battery paste. The effects of reducing agents, acid concentration, pulp density, reaction temperature, and leaching time on the dissolution of manganese and zinc were investigated in detail. Manganese dissolution by reductive acidic media is an intermediate-controlled process with an activation energy of 12.28 kJ·mol-1. After being leached, manganese and zinc were selectively precipitated with sodium hydroxide. The zinc was entirely converted into zincate (Zn(OH){4/2-}) ions and thus did not co-precipitate with manganese hydroxide during this treatment (2.0 M NaOH, 90 min, 200 r/min, pH > 13). After the manganese was removed from the solution, the Zn(OH){4/2-} was precipitated as zinc sulfate in the presence of sulfuric acid. The results indicated that this process could be effective in recovering manganese and zinc from alkaline batteries.

  18. Electrochemistry in aqueous solution at high temperature and under pressure: study of nickel in a highly alkaline environment

    International Nuclear Information System (INIS)

    This research thesis reports the study of the corrosion resistance and anodic behaviour of various metals and alloys used in conventional thermal or nuclear power stations, more particularly the case of nickel in a highly alkaline environment (KOH 5 N) which is widely used for hydrogen production by water electrolysis. The author studied the influence of temperature and pressure on the electrochemical behaviour of nickel, and more particularly the first-oxidation kinetics. The report discusses the physicochemical and thermodynamic properties of aqueous systems at high temperature and under pressure, presents the general techniques of high-temperature electrochemistry, describes the experimental installation, and reports the development of a reference electrode which can operate in those experimental conditions. The author reports the study of the electrochemical behaviour of nickel in alkaline environment and at high temperature, reports a surface analysis performed by Auger spectroscopy, electron spectroscopy for chemical analysis or ESCA, and scanning electronic microscopy, reports the study of the electrochemical behaviour of nickel in a potassium hydroxide solution under normal temperature and pressure, but also in acid environment. Results are interpreted with respect to temperature

  19. Modeling solute in clays at the nano-metric scale Part I. Application to the alkaline series

    International Nuclear Information System (INIS)

    The argillite formation has been proposed as a potential host rock for deep radioactive waste disposal. These materials have very low permeability and diffusion is likely to be the predominant transfer mechanism for solute migration.The negatively charged surface of the clays induces unexpected behaviour of the ions: while the anions diffuse slower than HTO, the transport of the cations is accelerated. To explain these two antagonistic phenomena, 'effective diffusion porosity' for anions and 'surface diffusion' for cations has usually been introduced. The aim of the present study is to describe the main mechanism that takes place in the vicinity of the charged surface (nano-metric scale) and enables to quantify the behaviour of the alkaline series (from Li to Cs), i.e increase the retention and effective diffusion coefficient from lithium to caesium. This model with few inputs can quantitatively reproduced specific adsorption of monovalent cations and adsorption isotherm for Rb, Cs. Hydration and electrostatic forces seem to be the main interactions controlling the adsorption on surface for the alkaline series. (authors)

  20. Ultrafiltration ceramic membrane performance during the treatment of model solutions containing dye and salt

    OpenAIRE

    Alventosa De Lara, Elena; Barredo Damas, Sergio; Zuriaga Agusti, Elena; Alcaina Miranda, María Isabel; Iborra Clar, María Isabel

    2014-01-01

    The present study reports the results of the ultrafiltration with a ceramic membrane of model solutions containing NaCl and a reactive dye, which simulate textile wastewaters. The effect of salt concentration (1, 2.5 and 4 g/L NaCl) and transmembrane pressure (1, 2, and 3 bar) on the evolution over time of both permeate flux and solutes rejection was tested. Membrane fouling was also investigated in terms of analysis of resistances-in-series, determining the contribution of both reversible an...

  1. Atomistic description of binary lanthanoid salt solutions: A coarse-graining approach

    International Nuclear Information System (INIS)

    The experimental difficulties inherent to the solution chemistry of actinoids and lanthanoids have led to the use of a wide variety of models, from the microscopic to the macroscopic scale, in an attempt to represent their solution properties. Molecular dynamics (MD) simulations, with explicit solvents, have been successfully used to describe the structural characteristics, but the limits on the accessible length and time scales do not allow for an equivalent description of the macroscopic properties. In this study, we propose a multi-scale approach, based on MD simulation results, to study the thermodynamic and structural properties of a series of lanthanoid-chloride aqueous solutions. An inversion procedure, based on the approximate hypernetted chain (HNC) closure and the Stillinger-Lovett sum rules for ionic liquids, is used to obtain the effective ion-ion potentials from MD-generated radial distribution functions (RDF). Implicit solvent Monte Carlo (MC) simulations are then performed to compute the osmotic coefficients of the salt solutions. This coarse-grained strategy provides accurate effective pair potentials for the lanthanoid salts, derived from an atomic model. The method presented here is an attempt to bridge the gap between MD and the thermodynamic properties of solutions that are experimentally measured. (authors)

  2. Alternative solvent wash process using tetramethylammonium hydroxide solution as salt-free wash reagent

    International Nuclear Information System (INIS)

    A solvent wash procedure employing tetramethylammonium hydroxide (TMAH) as an alternative to sodium carbonate was investigated in order to minimize the volume of radioactive waste resulting from solvent regeneration in the Purex process. The wash efficiency of tetramethylammonium base solutions was measured in comparison with sodium carbonate solution on a 30 % TBP-70 % dodecane mixture containing zirconium-dibutyl phosphate complex. The experimental evidence showed tetrametylammonium base solutions to be as effective as sodium carbonate solution. In particular, addition of oxalic acid which complexes strongly with zirconium enhanced the wash efficiency. The 31P NMR spectra of dibutyl phosphate (DBP) indicated that the cleanup of DBP depended mainly on ionization of DBP. As tetrametylammonium hydroxide can be decomposed by heating at about 200deg C, it is considered to have good applicability as a salt-free wash reagent. (author)

  3. In situ generated highly active copper oxide catalysts for the oxygen evolution reaction at low overpotential in alkaline solutions.

    Science.gov (United States)

    Liu, Xiang; Cui, Shengsheng; Qian, Manman; Sun, Zijun; Du, Pingwu

    2016-04-25

    Developing efficient water oxidation catalysts made up of earth-abundant elements has attracted much attention as a step toward for future clean energy production. Herein we report a simple one-step method to generate a low cost copper oxide catalyst film in situ from a copper(ii) ethylenediamine complex. The resulting catalyst has excellent activity toward the oxygen evolution reaction in alkaline solutions. A catalytic current density of 1.0 mA cm(-2) and 10 mA cm(-2) for the catalyst film requires the overpotentials of only ∼370 mV and ∼475 mV in 1.0 M KOH, respectively. This catalytic performance shows that the new catalyst is one of the best Cu-based heterogeneous OER catalysts to date. PMID:27020763

  4. Kinetics of the hydrogen evolution on nickel in alkaline solution: new insight from rotating disk electrode and impedance spectroscopy analysis

    International Nuclear Information System (INIS)

    Nickel catalysts were characterized for the hydrogen evolution reaction (HER) using rotating disk electrode (RDE) and electrochemical impedance spectroscopy (EIS). The theoretical Levich slope was calculated on the basis of the HER mechanism in alkaline solution. Kinetic and thermodynamic parameters of the reaction were obtained for fresh polished nickel electrode (Nif), and for nickel after a quick chronoamperometric aging procedure (Nipc). Koutecky-Levich analysis indicated that the rate determining step on Nif is the one-electron Volmer reaction, while for Nipc decreases from one to 0.68 and exhibits a strong temperature dependence. A loss of catalytic activity, corresponding to an increase of 0.3 V of the HER onset potential, was observed after aging. Furthermore, from the EIS-Tafel analysis we concluded that the H adsorption changes from a Langmuir type for Nif, to a Temkin type for Nipc

  5. Study on Gold(Ⅰ) Solvent Extraction from Alkaline Cyanide Solution by TBP with Addition of Surfactant

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The new solvent extraction system for gold(Ⅰ) from alkaline cyanide solution by TBP with addition of surfactant in aqueous phase was studied. The effect of various factors, such as equilibrium pH, constitution of organic phase, molar ratio of CPB∶Au(CN)2-, extraction time, aqueous/organic phase ratio, different initial gold concentration, equilibrium temperature, different diluent, different types of extractants and surfactants etc., was inspected. The results show that gold(Ⅰ) can be extracted quantitatively by controlling the quantity of surfactant (CPB); both the equilibrium pH and diluent hardly influence percent extraction. Gold(Ⅰ) percent extraction reaches more than 98% under the optimal experimental conditions. 30% vol TBP diluted by sulphonating kerosene can load gold(Ⅰ) to rather high levels. Loading capacity is in excess of 38 g/L. The extraction mechanism is discussed and the overall extraction reaction is deduced.

  6. Severe corrosion of copper in a highly alkaline egg white solution due to a biuret corrosion reaction

    International Nuclear Information System (INIS)

    Highlights: • Egg whites can accelerate the corrosion of copper. • The corrosion rate of copper is closely related to the pH values. • The mechanism of the strong corrosion is due to a biuret corrosion reaction. - Abstract: Through investigating the interaction between copper metal and egg whites as well as the effects of pH, oxygen and the species of alkalis on copper corrosion rate, an unusual severe corrosion of copper metal in a highly alkaline egg white solution was found. The mechanism was investigated through detailed characterizations using a scanning electron microscope, X-ray diffraction, X-ray photoelectron spectroscopy and UV–visible absorption spectroscopy. The severe corrosion was mainly due to the formation of a hydroxyl–peptide–copper multicomponent stable soluble complex, which the biuret reaction also produces

  7. Separating nano graphene oxide from the residual strong-acid filtrate of the modified Hummers method with alkaline solution

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Xuebing, E-mail: xuebinghu2010@gmail.com [Key Laboratory of Inorganic Membrane, Jingdezhen Ceramic Institute, Jingdezhen 333001 (China); Key Laboratory of Inorganic Coating Materials, Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 201800 (China); Yu, Yun, E-mail: yunyush@mail.sic.ac.cn [Key Laboratory of Inorganic Coating Materials, Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 201800 (China); Wang, Yongqing; Zhou, Jianer [Key Laboratory of Inorganic Membrane, Jingdezhen Ceramic Institute, Jingdezhen 333001 (China); Song, Lixin [Key Laboratory of Inorganic Coating Materials, Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 201800 (China)

    2015-02-28

    Graphical abstract: By adding an alkaline (NaOH or KOH) solution, the unprecipitated nano graphene oxide undergoes fast aggregation from the residual strong-acid filtrate of the modified Hummers method and forms the stable floccules when the pH value of the filtrate is about 1.7. The acid–base interaction with the surface functional groups of the carbon layers plays a role in the aggregation of the unprecipitated nano graphene oxide. - Highlights: • The novel and high-efficient method for separating graphene oxide was showed. • Graphene oxide undergoes aggregation and forms the floccules when pH value is ∼1.7. • The acid–base interaction plays a role in the aggregation of graphene oxide. - Abstract: In the modified Hummers method for preparing graphene oxide, the yellow slurry can be obtained. After filtering through a quantitative filter paper, the strong-acid filtrate containing the unprecipitated nano graphene oxide was gained. The corresponding filtrate was added gradually with an alkaline (NaOH or KOH) solution at room temperature. The unprecipitated nano graphene oxide could undergo fast aggregation when the pH value of the filtrate was about 1.7 and formed the stable floccules. X-ray diffraction analysis shows the dominant peak of the floccules is about 11°, which accords to the peak of graphene oxide. Spectra of X-ray photoelectron spectroscopy confirm the presence in the floccules of an abundance of oxygen functional groups and the purified graphene oxide floccules can be obtained. Atomic force microscopy measurement shows the graphene oxide floccules consists of sheet-like objects, mostly containing only a few layers (about 5 layers). Zeta potential analysis demonstrates the surface charge of the graphene oxide is pH-sensitive and its isoelectric point is ∼1.7. The flocculation mechanism of graphene oxide ascribes to the acid–base interaction with the surface functional groups of the carbon layers.

  8. Oxygen reduction in alkaline solution using mixed carbon paste/NixCo1-xO electrodes

    International Nuclear Information System (INIS)

    Hydrogen peroxide is a valuable chemical used in various applications and there is a demand for small on-site production plants. An attractive way to produce hydrogen peroxide is by electrochemical reduction of oxygen, using electrocatalytic materials that favour formation of hydrogen peroxide instead of water. Oxygen reduction on carbon in alkaline solution is known to produce mainly hydrogen peroxide but the overpotential is large and electrocatalytic materials need to be used in combination with carbon. In the present study, the mechanism of oxygen reduction in alkaline solution was studied using NiO, Ni0.75Co0.25O and CoO powders in a matrix of carbon paste. The desired product is hydrogen peroxide and the rotating ring disc technique was used to measure the amount of hydrogen peroxide formed. Two separate processes are observed with a peak shaped wave at low overpotentials and a sigmoidal process at high overpotentials. The charge involved in the first process and the heterogeneous rate constant for the second process were determined and found to be higher in the presence of oxide compared to pure carbon paste. Maximum increase was found for the NiO containing electrode with five times higher charge in the low overpotential region and 25 times higher rate constant in the high overpotential region. The mechanism of oxygen reduction comprises redox mediated electron transfer reactions involving Ni(II)/Ni(III) states on the surface. In the low overpotential region, where oxygen reduction on carbon is mediated by native quinone groups, the increased activity is explained by an interplay between the quinone and Ni(OH)2/NiOOH redox couples

  9. Implications of alkaline solutions-induced etching on optical and minority carrier lifetime features of monocrystalline silicon

    Energy Technology Data Exchange (ETDEWEB)

    Bachtouli, N. [Photovoltaic Laboratory, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia); Aouida, S., E-mail: salma.aouida@crten.rnrt.tn [Photovoltaic Laboratory, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia); Laajimi, R. Hadj [Water Researches and Technologies Center, Science and Technology Park, BP 273, route touristique Soliman Borj-Cedria, 8020 Soliman (Tunisia); Department of Chemistry, College of Science, University of Hail, P.O. Box 1560, Hail (Saudi Arabia); Boujmil, M.F.; Bessais, B. [Photovoltaic Laboratory, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia)

    2012-09-01

    Highlights: Black-Right-Pointing-Pointer Three alkaline solutions: NaOH, KOH and TMAH are used to form pyramidal structure on silicon surface wafer. Black-Right-Pointing-Pointer The apex angle of the formed pyramids varies between 75 Degree-Sign and 82 Degree-Sign . Black-Right-Pointing-Pointer The heights and bases range from 230 nm to 30 {mu}m. Black-Right-Pointing-Pointer The photoconductivity enhancement is related to pyramidal sizes and reflectivity behavior Black-Right-Pointing-Pointer The QSSPC measurement reveals an apparent increase in the minority carrier lifetime. - Abstract: In this work, we search to optimize the surface textures of monocrystalline silicon (c-Si) intended to be used in silicon solar cells. For this purpose, we studied the morphology of formed etch hillocks during anisotropic etching of silicon using alkaline solutions based on sodium hydroxide (NaOH), potassium hydroxide (KOH) and tetramethylammonium hydroxide (TMAH). Such treatments lead to the formation of various pyramids-like textures that can be well optimized to improve the photocurrent of c-Si-based solar cells. The produced textures were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), UV-visible optical reflectivity and minority carrier lifetime measurements. These investigations allow evaluating the size and density of the formed pyramidal textures; the apex angles vary between 75 Degree-Sign and 82 Degree-Sign , while the heights and bases of the pyramids range from a few hundred nanometers to several micrometers. A minimum reflectivity value of about 6% was obtained at specific conditions using NaOH, whereas it was found that the apparent effective minority carrier lifetime ({tau}{sub eff}) is sensitive to the injection level ({Delta}n), which shows an apparent increase from 1.2 {mu}s to 2.4 {mu}s for a minority carrier density of about {Delta}n = 210{sup 14} cm{sup -3}.

  10. Implications of alkaline solutions-induced etching on optical and minority carrier lifetime features of monocrystalline silicon

    International Nuclear Information System (INIS)

    Highlights: ► Three alkaline solutions: NaOH, KOH and TMAH are used to form pyramidal structure on silicon surface wafer. ► The apex angle of the formed pyramids varies between 75° and 82°. ► The heights and bases range from 230 nm to 30 μm. ► The photoconductivity enhancement is related to pyramidal sizes and reflectivity behavior ► The QSSPC measurement reveals an apparent increase in the minority carrier lifetime. - Abstract: In this work, we search to optimize the surface textures of monocrystalline silicon (c-Si) intended to be used in silicon solar cells. For this purpose, we studied the morphology of formed etch hillocks during anisotropic etching of silicon using alkaline solutions based on sodium hydroxide (NaOH), potassium hydroxide (KOH) and tetramethylammonium hydroxide (TMAH). Such treatments lead to the formation of various pyramids-like textures that can be well optimized to improve the photocurrent of c-Si-based solar cells. The produced textures were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), UV–visible optical reflectivity and minority carrier lifetime measurements. These investigations allow evaluating the size and density of the formed pyramidal textures; the apex angles vary between 75° and 82°, while the heights and bases of the pyramids range from a few hundred nanometers to several micrometers. A minimum reflectivity value of about 6% was obtained at specific conditions using NaOH, whereas it was found that the apparent effective minority carrier lifetime (τeff) is sensitive to the injection level (Δn), which shows an apparent increase from 1.2 μs to 2.4 μs for a minority carrier density of about Δn = 21014 cm−3.

  11. Separating nano graphene oxide from the residual strong-acid filtrate of the modified Hummers method with alkaline solution

    International Nuclear Information System (INIS)

    Graphical abstract: By adding an alkaline (NaOH or KOH) solution, the unprecipitated nano graphene oxide undergoes fast aggregation from the residual strong-acid filtrate of the modified Hummers method and forms the stable floccules when the pH value of the filtrate is about 1.7. The acid–base interaction with the surface functional groups of the carbon layers plays a role in the aggregation of the unprecipitated nano graphene oxide. - Highlights: • The novel and high-efficient method for separating graphene oxide was showed. • Graphene oxide undergoes aggregation and forms the floccules when pH value is ∼1.7. • The acid–base interaction plays a role in the aggregation of graphene oxide. - Abstract: In the modified Hummers method for preparing graphene oxide, the yellow slurry can be obtained. After filtering through a quantitative filter paper, the strong-acid filtrate containing the unprecipitated nano graphene oxide was gained. The corresponding filtrate was added gradually with an alkaline (NaOH or KOH) solution at room temperature. The unprecipitated nano graphene oxide could undergo fast aggregation when the pH value of the filtrate was about 1.7 and formed the stable floccules. X-ray diffraction analysis shows the dominant peak of the floccules is about 11°, which accords to the peak of graphene oxide. Spectra of X-ray photoelectron spectroscopy confirm the presence in the floccules of an abundance of oxygen functional groups and the purified graphene oxide floccules can be obtained. Atomic force microscopy measurement shows the graphene oxide floccules consists of sheet-like objects, mostly containing only a few layers (about 5 layers). Zeta potential analysis demonstrates the surface charge of the graphene oxide is pH-sensitive and its isoelectric point is ∼1.7. The flocculation mechanism of graphene oxide ascribes to the acid–base interaction with the surface functional groups of the carbon layers

  12. Molecular Thermodynamics for Swelling of a Mesoscopic Ionomer Gelin 1:1 Salt Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Victorov, Alexey; Radke, Clayton; Prausnitz,John

    2005-06-15

    For a microphase-separated diblock copolymer ionic gel swollen in salt solution, a molecular-thermodynamic model is based on the self-consistent field theory in the limit of strongly segregated copolymer subchains. The geometry of microdomains is described using the Milner generic wedge construction neglecting the packing frustration. Thermodynamic functions are expressed analytically for gels of lamellar, bicontinuous, cylindrical and spherical morphologies. Molecules are characterized by chain composition, length, rigidity, degree of ionization, and by effective polymer-polymer and polymer-solvent interaction parameters. The model predicts equilibrium solvent uptakes and the equilibrium microdomain spacing for gels swollen in salt solutions. Results are given for details of the gel structure: distribution of mobile ions and polymer segments, and the electric potential across microdomains. Apart from effects obtained by coupling classical Flory-Rehner theory with Donnan equilibria, viz., increased swelling with polyelectrolyte charge and shrinking of gel upon addition of salt, the model predicts the effects of microphase morphology on swelling.

  13. Electrodeposition and characterization of Ni-MoO2 composite coatings as cathodes for the hydrogen evolution reaction in alkaline solution

    OpenAIRE

    Lačnjevac Uroš Č.

    2013-01-01

    Composite Ni-MoO2 coatings were prepared and characterized with respect to their possible application as electrocatalysts for the hydrogen evolution reaction (HER) in alkaline solution. The composites were electrodeposited onto Ni meshes from an ammonium chloride Ni solution with suspended MoO2 particles in simulated industrial conditions for production of commercial cathodes. The influence of the concentration of MoO2 particles in the solution and deposition current density on the morp...

  14. Molecular dynamics study of salt–solution interface: Solubility and surface charge of salt in water

    International Nuclear Information System (INIS)

    The NaCl salt–solution interface often serves as an example of an uncharged surface. However, recent laser-Doppler electrophoresis has shown some evidence that the NaCl crystal is positively charged in its saturated solution. Using molecular dynamics (MD) simulations, we have investigated the NaCl salt–solution interface system, and calculated the solubility of the salt using the direct method and free energy calculations, which are kinetic and thermodynamic approaches, respectively. The direct method calculation uses a salt–solution combined system. When the system is equilibrated, the concentration in the solution area is the solubility. In the free energy calculation, we separately calculate the chemical potential of NaCl in two systems, the solid and the solution, using thermodynamic integration with MD simulations. When the chemical potential of NaCl in the solution phase is equal to the chemical potential of the solid phase, the concentration of the solution system is the solubility. The advantage of using two different methods is that the computational methods can be mutually verified. We found that a relatively good estimate of the solubility of the system can be obtained through comparison of the two methods. Furthermore, we found using microsecond time-scale MD simulations that the positively charged NaCl surface was induced by a combination of a sodium-rich surface and the orientation of the interfacial water molecules

  15. Influence of water and salt solutions on UVB irradiation of normal skin and psoriasis

    International Nuclear Information System (INIS)

    The influence of tap-water (TW) and salt solutions on the minimal erythema dose (MED) was investigated for normal human skin and uninvolved skin of psoriasis patients. MED (UVB) determinations on the forearm revealed that: (1) the MED definitely decreases whenever the arm is immersed in TW or NaCl solutions with a low concentration (4%) prior to UVB exposure, whereas almost saturated NaCl solution (26%), as well as locum Dead Sea water (LDSW), do not produce a change in the MED, and (2) the decrease in MED obtained by wetting the skin with TW was no longer present when the skin was allowed to dry for 20 min. A decrease in water uptake by skin (in vivo) and by callus (in vitro) was found as the salt concentration of the external solution increased. It is proposed that water taken up by the skin plays an important role in the sensitivity of the skin to UVB exposure. Bathing in TW or 4% NaCl prior to UVB exposure offered a slight to moderate improvement in psoriasis over UVB irradiation alone. Finally, it was shown that there is no obvious difference in clearance of the psoriatic skin between a bath in TW, 4% NaCl, or LDSW prior to UVB exposure. (orig.)

  16. Radiation effects in frozen solutions of iron salts and solid state dosimeters at low temperatures

    International Nuclear Information System (INIS)

    Low temperature dosimetry is useful in space research, in the simulation of reactions that may take place in extraterrestrial icy-bodies, etc. In this paper we study the behavior of three different systems in order to evaluate if they can be used as dosimeters at low temperatures. The systems under study are 1) frozen solutions of iron salts, 2) crystals of LiF co-doped with Mg, Cu and P, and 3) crystals of CaSO4 doped with Dy. For the frozen solution the analysis was performed after melting by UV-spectroscopy and for the crystals the response was measured by thermoluminescence. The systems were irradiated with gamma radiation at different doses (from 10 to 2500 Gy), and at different temperatures (from 77 K to 298 K). Numerical simulations of the chemical reaction system reproduce the experimental effects produced by the irradiation in aqueous solutions of ferrous salt. The results with both the thermoluminescence dosimeters and the frozen iron aqueous solutions showed that the response of the dosimeters is a function of the temperature. At low radiation doses the response was linear. (Author)

  17. Study on Properties of Microemulsion AEO-9/Butanol/Cyclohexane/Salt Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    Qiu Guanming; Chen Yongjie; Tian Yiguang; Fang Li; Xiao Linjiu; Sun Yanbin

    2004-01-01

    The microemulsion AEO-9/butanol/cyclohexane/nitrate aqueous solution (or ammonium salt aqueous solution) was studied, which was used as 'micro-reactor' in preparing long afterglow phosphor materials SrAl2O4: Eu2+ ,Dy3+. The phase behavior of microemulsion was investigated. The radius of inner water droplet Rw and the change of standard free energy ΔG*o→i were obtained by means of dilution method and theoretical calculation. The result shows that with the increase of W/S, the area of microemulsion region decreases, Rw and ΔG*o→i increase and the microemulsion stability decreases. The structure change and formation area of microemulsion AEO-9/butanol/cyclohexane/nitrate aqueous solution ( or ammonium salt aqueous solution) were offered for the adoption of a synthesis method with newly high efficiency and utility. The particular size and its distribution theory gist, fluorescence life-span, and quenching concentration parameter data were expected. A new approach was explored for finding a new preparation method of rare earths afterglow materials and increasing luminescence intensity without crashing.

  18. A Chronoamperometric Screen Printed Carbon Biosensor Based on Alkaline Phosphatase Inhibition for W(VI Determination in Water, Using 2-Phospho-l-Ascorbic Acid Trisodium Salt as a Substrate

    Directory of Open Access Journals (Sweden)

    Ana Lorena Alvarado-Gámez

    2015-01-01

    Full Text Available This paper presents a chronoamperometric method to determine tungsten in water using screen-printed carbon electrodes modified with gold nanoparticles and cross linked alkaline phosphatase immobilized in the working electrode. Enzymatic activity over 2-phospho-l-ascorbic acid trisodium salt, used as substrate, was affected by tungsten ions, which resulted in a decrease of chronoamperometric current, when a potential of 200 mV was applied on 10 mM of substrate in a Tris HCl buffer pH 8.00 and 0.36 M of KCl. Calibration curves for the electrochemical method validation, give a reproducibility of 5.2% (n = 3, a repeatability of 9.4% (n = 3 and a detection limit of 0.29 ± 0.01 µM. Enriched tap water, purified laboratory water and bottled drinking water, with a certified tungsten reference solution traceable to NIST, gave a recovery of 97.1%, 99.1% and 99.1% respectively (n = 4 in each case and a dynamic range from 0.6 to 30 µM. This study was performed by means of a Lineweaver–Burk plot, showing a mixed kinetic inhibition.

  19. On the decay of the ozonide radical in aqueous alkaline solutions

    Science.gov (United States)

    Bhattacharyya, P. K.; Saini, R. D.

    1982-11-01

    In flash photolysis of an oxygenated aqueous potassium persulphate solution at pH 12.5 the decay of the ozonide radical has been found to follow 3/2 order kinetics which has been explained by reactions O -3 + O - ⇌ 2 O -2 and O -3 + HO 2 → 2 O 2 + OH -

  20. Recovery of uranium from alkaline ore (Tummalapalle) leach solution using novel precipitating method

    International Nuclear Information System (INIS)

    The aim of present study is recovery of uranium from such ore leach solution containing 2O7 at pH ∼12.5. The average particle size of the MgU2O7 particles was 20 micron and overall uranium recovery was 97%. The composition of final precipitate was characterized using XRD and surface morphology was studied using SEM

  1. Oral salt supplements to compensate for jejunostomy losses: comparison of sodium chloride capsules, glucose electrolyte solution, and glucose polymer electrolyte solution.

    OpenAIRE

    Nightingale, J M; Lennard-Jones, J E; Walker, E. R.; Farthing, M J

    1992-01-01

    Six patients with jejunostomies and residual jejunal lengths of 105 to 250 cm took the same food and water each day for eight study days. In random order, three methods of salt replacement were tested, each over 48 hours, against a period without added salt. During the three test periods the patients took 120 mmol of sodium chloride daily, as salt in gelatine capsules, as an isotonic glucose electrolyte (280 mOsmol/kg; 30 kcal) solution, and as a glucose polymer (Maxijul) solution (280 mOsmol...

  2. Alkaline iron(III) reduction by a novel alkaliphilic, halotolerant, Bacillus sp. isolated from salt flat sediments of Soap Lake.

    Science.gov (United States)

    Pollock, Jarrod; Weber, Karrie A; Lack, Joe; Achenbach, Laurie A; Mormile, Melanie R; Coates, John D

    2007-12-01

    A halotolerant, alkaliphilic dissimilatory Fe(III)-reducing bacterium, strain SFB, was isolated from salt flat sediments collected from Soap Lake, WA. 16S ribosomal ribonucleic acid gene sequence analysis identified strain SFB as a novel Bacillus sp. most similar to Bacillus agaradhaerens (96.7% similarity). Strain SFB, a fermentative, facultative anaerobe, fermented various hexoses including glucose and fructose. The fructose fermentation products were lactate, acetate, and formate. Under fructose-fermenting conditions in a medium amended with Fe(III), Fe(II) accumulated concomitant with a stoichiometric decrease in lactate and an increase in acetate and CO(2). Strain SFB was also capable of respiratory Fe(III) reduction with some unidentified component(s) of Luria broth as an electron donor. In addition to Fe(III), strain SFB could also utilize nitrate, fumarate, or O(2) as alternative electron acceptors. Optimum growth was observed at 30 degrees C and pH 9. Although the optimal salinity for growth was 0%, strain SFB could grow in a medium with up to 15% NaCl by mass. These studies describe a novel alkaliphilic, halotolerant organism capable of dissimilatory Fe(III) reduction under extreme conditions and demonstrate that Bacillus species can contribute to the microbial reduction of Fe(III) in environments at elevated pH and salinity, such as soda lakes. PMID:17943280

  3. RESULTS OF ANALYSES OF MACROBATCH 3 DECONTAMINATED SALT SOLUTION (DSS) COALESCER AND PRE-FILTERS

    Energy Technology Data Exchange (ETDEWEB)

    Peters, T.; Fondeur, F.; Fink, S.

    2012-06-13

    SRNL analyzed the pre-filter and Decontamination Salt Solution (DSS) coalescer from MCU by several analytical methods. The results of these analyses indicate that overall there is light to moderate solids fouling of both the coalescer and pre-filter elements. The majority of the solids contain aluminum, sodium, silicon, and titanium, in oxide and/or hydroxide forms that we have noted before. The titanium is presumably precipitated from leached, dissolved monosodium titanate (MST) or fines from MST at ARP, and the quantity we find is significantly greater than in the past. A parallel report discusses potential causes for the increased leaching rate of MST, showing that increases in free hydroxide concentration of the feed solutions and of chemical cleaning solutions lead to faster leaching of titanium.

  4. Interaction of molybdophosphates with palladium(II) salts in aqueous solutions

    International Nuclear Information System (INIS)

    The methods of electron and 31P NMR spectroscopies were used to study the interaction of H3PMo12O40 with H2PdCl4 or PdSO4 in aqueous solution at pH 3.0-4.5 and the ratio [Pd(II)]:[H3PMo12O40]=1:1. Palladium(II) remains in solution in the form of intensely colored hydroxo species and does not change the structure of the newly formed unsaturated heteropolymolybdates PMo11O397- and PMo9O349- as shown by NMR data. Heteropoly compounds precipitated from tetrabutylammonium or cesium salts were characterized using IR spectroscopy, differential dissolution and elemental analysis. It was found that the composition of a compound was affected by not only formation conditions in the solution but also the precipitant cation

  5. Can mothers safely prepare labon-gur salt-sugar solution after demonstration in a diarrhoeal hospital?

    DEFF Research Database (Denmark)

    Islam, M A; Kofoed, Poul-Erik; Begum, S

    1992-01-01

    Home-based salt-sugar solution (SSS) prepared with labon (locally produced sea salt) and gur (unrefined brown sugar) has been recommended as a cheap, locally available and a simple tool to prevent and treat diarrhoeal dehydration. Preparation of labon-gur SSS is demonstrated to the patients and the...... while 1.3% exceeded the upper danger limit for salt and 98.7% samples of gur were within safe and effective range. Mothers' performances were not different with regard to their educational status and prior practice at home. 80% knew about the solution before coming to the hospital and 45% had utilized...

  6. On the radiolysis of concentrated alkaline and calcium-nitrate solutions

    International Nuclear Information System (INIS)

    Previous studies have shown that more nitrite is produced than can reasonably be accounted for by an indirect radiolysis mechanism based on the radical products of radiolysed water. Further results on the relative roles of indirect effect and direct effect (a chemical transformation in the solute due to its energy absorption) are presented. Major products are nitrite, peroxide and oxygen and yields can be accounted for using the electron fraction model. (author)

  7. Preparation and Characterization of Organic-Inorganic Hybrid Hydrogel Electrolyte Using Alkaline Solution

    OpenAIRE

    Masanobu Chiku; Shoji Tomita; Eiji Higuchi; Hiroshi Inoue

    2011-01-01

    Organic-inorganic hybrid hydrogel electrolytes were prepared by mixing hydrotalcite, cross-linked potassium poly(acrylate) and 6 M KOH solution. The organic-inorganic hybrid hydrogel electrolytes had high ionic conductivity (0.456–0.540 S cm−1) at 30 °C. Moreover, the mechanical strength of the hydrogel electrolytes was high enough to form a 2–3 mm thick freestanding membrane because of the reinforcement with hydrotalcite.

  8. Forecasting of thermodynamic properties of solution for non-polar molecules in aqueous salt solutions and in aqueous organic solutions

    International Nuclear Information System (INIS)

    The scaled particle theory has been used rather successfully to predict the values of thermodynamic properties of solution for non-polar molecules. Two very important parameters has been used in the equations of the scaled particle theory: the hard sphere diameter of the solute and the closeness of the solvent (closeness in which the diameters of the hard sphere particles forming the solvent are taken into account). With non-polar solutes, a correlation exists between calculated and experimental values of: free enthalpy of solution - enthalpy of solution - molar heat capacity change for the solution process. The fit between calculated and experimental values is only more qualitative than quantitative. However the variation of thermodynamic properties with the temperature and the modality is consistent with the variation calculated according to the scaled particle theory. (author)

  9. Evaluating Battery-like Reactions to Harvest Energy from Salinity Differences using Ammonium Bicarbonate Salt Solutions.

    Science.gov (United States)

    Kim, Taeyoung; Rahimi, Mohammad; Logan, Bruce E; Gorski, Christopher A

    2016-05-10

    Mixing entropy batteries (MEBs) are a new approach to generate electricity from salinity differences between two aqueous solutions. To date, MEBs have only been prepared from solutions containing chloride salts, owing to their relevance in natural salinity gradients created from seawater and freshwater. We hypothesized that MEBs could capture energy using ammonium bicarbonate (AmB), a thermolytic salt that can be used to convert waste heat into salinity gradients. We examined six battery electrode materials. Several of the electrodes were unstable in AmB solutions or failed to produce expected voltages. Of the electrode materials tested, a cell containing a manganese oxide electrode and a metallic lead electrode produced the highest power density (6.3 mW m(-2) ). However, this power density is still low relative to previously reported NaCl-based MEBs and heat recovery systems. This proof-of-concept study demonstrated that MEBs could indeed be used to generate electricity from AmB salinity gradients. PMID:27030080

  10. Equilibrium, kinetic and thermodynamic study of cesium adsorption onto nanocrystalline mordenite from high-salt solution.

    Science.gov (United States)

    Lee, Keun-Young; Park, Minsung; Kim, Jimin; Oh, Maengkyo; Lee, Eil-Hee; Kim, Kwang-Wook; Chung, Dong-Yong; Moon, Jei-Kwon

    2016-05-01

    In this study, the equilibrium, kinetics and thermodynamics of cesium adsorption by nanocrystalline mordenite were investigated under cesium contamination with high-salt solution, simulating the case of an operation and decommissioning of nuclear facilities or an accident during the processes. The adsorption rate constants were determined using a pseudo second-order kinetic model. The kinetic results strongly demonstrated that the cesium adsorption rate of nano mordenite is extremely fast, even in a high-salt solution, and much faster than that of micro mordenite. In the equilibrium study, the Langmuir isotherm model fit the cesium adsorption data of nano mordenite better than the Freundlich model, which suggests that cesium adsorption onto nano mordenite is a monolayer homogeneous adsorption process. The obtained thermodynamic parameters indicated that the adsorption involved a very stable chemical reaction. In particular, the combination of rapid particle dispersion and rapid cesium adsorption of the nano mordenite in the solution resulted in a rapid and effective process for cesium removal without stirring, which may offer great advantages for low energy consumption and simple operation. PMID:26683820

  11. Hydraulic conductivity in response to exchangeable sodium percentage and solution salt concentration

    Directory of Open Access Journals (Sweden)

    Jefferson Luiz de Aguiar Paes

    2014-10-01

    Full Text Available Hydraulic conductivity is determined in laboratory assays to estimate the flow of water in saturated soils. However, the results of this analysis, when using distilled or deionized water, may not correspond to field conditions in soils with high concentrations of soluble salts. This study therefore set out to determine the hydraulic conductivity in laboratory conditions using solutions of different electrical conductivities in six soils representative of the State of Pernambuco, with the exchangeable sodium percentage adjusted in the range of 5-30%. The results showed an increase in hydraulic conductivity with both decreasing exchangeable sodium percentage and increasing electrical conductivity in the solution. The response to the treatments was more pronounced in soils with higher proportion of more active clays. Determination of hydraulic conductivity in laboratory is routinely performed with deionized or distilled water. However, in salt affected soils, these determinations should be carried out using solutions of electrical conductivity different from 0 dS m-1, with values close to those determined in the saturation extracts.

  12. A novel technique of in situ phase-shift interferometry applied for faint dissolution of bulky montmorillonite in alkaline solution

    International Nuclear Information System (INIS)

    The effect of alkaline pH on the dissolution rate of bulky aggregated montmorillonite samples at 23°C was investigated for the first time by using an enhanced phase-shift interferometry technique combined with an internal refraction interferometry method developed for this study. This technique was applied to provide a molecular resolution during the optical observation of the dissolution phenomena in real time and in situ while remaining noninvasive. A theoretical normal resolution limit of this technique was 0.78 nm in water for opaque material, but was limited to 6.6 nm for montmorillonite due to the transparency of the montmorillonite crystal. Normal dissolution velocities as low as 1 × 10-4 to 1 × 10-3 nm/s were obtained directly by using the measured temporal change in height of montmorillonite samples set in a reaction cell. The molar dissolution fluxes of montmorillonite obtained in this study gave considerably faster dissolution rates in comparison to those obtained in previous investigations by solution analysis methods. The pH dependence of montmorillonite dissolution rate determined in this study was qualitatively in good agreement with those reported in the previous investigations. The dissolution rates to be used in safety assessments of geological repositories for radioactive wastes should be obtained for bulky samples. This goal has been difficult to achieve using conventional powder experiment technique and solution analysis method, but has been shown to be feasible using the enhanced phase-shift interferometry. (author)

  13. CO2 Capture from Flue gas using Amino acid salt solutions

    DEFF Research Database (Denmark)

    Lerche, Benedicte Mai

    naturally occurring substances, and partly because they have desirable properties, such as lower vapor pressures and higher stability against oxidative degradation. One important feature of these new solvents is the formation of solids upon CO2 absorption, which happens especially at higher CO2 loadings and...... of the components in the apparatus. Ideally, measurements in the full temperature range for desorption, which usually needs approximately 393 K (120 ºC), would be desirable. Using the 2 apparatuses, CO2 solubility in aqueous solutions of MEA and the potassium salts of taurine, glycine, L-alanine, L...

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

    DEFF Research Database (Denmark)

    Christoffersen, Gert Rene Juul; Skibsted, Leif H

    1975-01-01

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

  15. Investigation of processes accompanying synthesis of oxide compounds from salt polymer-containing solutions

    International Nuclear Information System (INIS)

    Using a complex of physicochemical methods (thermal and X-ray phase analyses, dilatometry, microscopy, study of temperature dependences of film adhesion to substrates and their electric conductivity), processes of synthesis and film formation of high Tc superconductor materials of the composition YBa2Cu3O7-δ from aqueous formate and nitrate solutions, containing polyvinyl alcohol, have been investigated. It is shown that the salt systems studied, which contain a water-soluble polymer, are of practical and scientific value. The complex of the methods suggested provides objective and reliable information on the processes studied

  16. The solubility of amorphous and crystalline schoepite in neutral to alkaline aqueous solutions

    International Nuclear Information System (INIS)

    The solubility of schoepite UO2(OH)2H2O has been investigated by potentiometric titration at 250C in 0.5 mol dm.-3NaCIO4 solution. The data indicates the predominance of the species (UO2)3(OH)5+ and either UO2(OH)3- or (UO2)3)(OH)7- in the pH range studied. The formation constants of these species as well as the solubility product of the amorphous and microcrystalline schoepite have been determined. The consequences of these data on the hypothesis of schoepite as the solubility limiting phase in spent fuel dissolution studies is discussed

  17. Study of the extraction of heptavalent neptunium by phenolic extragents from strong alkaline solutions

    International Nuclear Information System (INIS)

    Regularities of neptunium(6) extractional behaviour from alkali solutions using aminomethyl derivatives of substituted phenols and alkylphenol oligomers were revealed. The maximum extraction is observed in conditions, where neptunium is present in the form of hydroxoions. Complexing of neptunium by metal substitution for extractant hydroxyl group protons was confirmed. It is assumed that the rate of Np(7) reduction to Np(6) increases with an increase in extractant concentration and extraction duration. Hexavalent neptunium is extracted by phenol extractants more slowly and with lower distribution coefficients than Np(7)

  18. Oxygen reduction at platinum nanoparticles supported on carbon cryogel in alkaline solution

    OpenAIRE

    N. R. ELEZOVIC; B. M. BABIC; Vracar, Lj. M.; N. V. KRSTAJIC

    2007-01-01

    The oxygen reduction reaction was investigated in 0.1 M NaOH solution, on a porous coated electrode formed of Pt particles supported on carbon cryogel. The Pt/C catalyst was characterized by the X-ray diffraction (XRD), transmission electron microscopy (TEM) and cyclic voltammetry techniques. The results demonstrated a successful reduction of Pt to metallic form and homogenous Pt particle size distribution with a mean particle size of about 2.7 nm. The ORR kinetics was investigated by linear ...

  19. Electrolytic decontamination of the dismantled metallic wastes contaminated with uranium compounds in neutral salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Wang Kyu; Lee, Sung Yeal; Kim, Kye Nam; Won, Hee Jun; Jung, Jong Heon; Oh, Won Zin [KAERI, Taejon (Korea, Republic of)

    2004-07-01

    Electrolytic dissolution study was carried out to evaluate the applicability of electrochemical decontamination process using a neutral salt electrolyte as a decontamination technology for the recycle or self disposal with authorization of large amount of metallic wastes contaminated with uranium compounds generated by dismantling a retired uranium conversion plant using SUS-304 and Inconel-600 specimen as the main materials of internal system components of the plant. The effects of type of neutral salt as an electrolyte, current density, and concentration of electrolyte on the dissolution of the materials were evaluated. On the basis of the results obtained through the basic inactive experiments, electrochemical decontamination tests using the specimens contaminated with uranium compounds such as UO{sub 2}, AUC (ammonium uranyl carbonate) and ADU (ammonium diuranate) taken from an uranium conversion plant were performed in Na{sub 2}SO{sub 4} and NaNO{sub 3} solution. It was verified that the electrochemical decontamination of the dismantled metallic wastes was quite successful in Na{sub 2}SO{sub 4} and NaNO{sub 3} neutral salt electrolyte by reducing {beta} radioactivities below the level of self disposal with authorization within 10 minutes regardless of the type of contaminants and the degree of contamination.

  20. Diffusion coefficients of β-cyclodextrin sulfated sodium salt in aqueous solutions

    International Nuclear Information System (INIS)

    Graphical abstract: Structure of β-cyclodextrin sulfated sodium salt. - Highlights: • Mutual diffusion coefficients of β-cyclodextrin sulfated sodium salt (NaSO3βCD) in aqueous solutions were measured. • Influence of the viscosity, thermodynamic and temperature factors on the variation of diffusion was analysed. • Estimation of the hydrodynamic radius of NaSO3βCD was obtained. - Abstract: The Taylor dispersion technique has been used for measuring mutual diffusion coefficients of β-cyclodextrin sulfated sodium salt (NaSO3βCD) at temperatures (298.15 and 310.15) K and at finite concentrations. These studies have been complemented by density and viscosity measurements. From these experimental results, the hydrodynamic radius Rh, and its dependence on the viscosity, diffusion coefficient at infinitesimal concentration, D0, ion conductivity of NaSO3βCD and the thermodynamic factor, FT, have been estimated, permitting us to have a better understanding of the structure of the aqueous system containing NaSO3βCD

  1. Electrolytic decontamination of the dismantled metallic wastes contaminated with uranium compounds in neutral salt solutions

    International Nuclear Information System (INIS)

    Electrolytic dissolution study was carried out to evaluate the applicability of electrochemical decontamination process using a neutral salt electrolyte as a decontamination technology for the recycle or self disposal with authorization of large amount of metallic wastes contaminated with uranium compounds generated by dismantling a retired uranium conversion plant using SUS-304 and Inconel-600 specimen as the main materials of internal system components of the plant. The effects of type of neutral salt as an electrolyte, current density, and concentration of electrolyte on the dissolution of the materials were evaluated. On the basis of the results obtained through the basic inactive experiments, electrochemical decontamination tests using the specimens contaminated with uranium compounds such as UO2, AUC (ammonium uranyl carbonate) and ADU (ammonium diuranate) taken from an uranium conversion plant were performed in Na2SO4 and NaNO3 solution. It was verified that the electrochemical decontamination of the dismantled metallic wastes was quite successful in Na2SO4 and NaNO3 neutral salt electrolyte by reducing β radioactivities below the level of self disposal with authorization within 10 minutes regardless of the type of contaminants and the degree of contamination

  2. Red-emitting alkaline-earth rare-earth pentaoxometallates powders prepared by metal carboxylates solution

    Indian Academy of Sciences (India)

    Kyu-Seog Hwang; Sung-Dae Kim; Seung Hwangbo; Jin-Tae Kim

    2013-06-01

    Moisture-insensitive metal carboxylates that are mostly liquids at room temperature have been first applied to the preparation of strontium europium aluminate (Sr2EuAlO5) powders for red-emitting phosphor under near ultraviolet radiation. Strontium naphthenate, aluminium-2-ethylhexanoate and europium-2-ethylhexanoate were dissolved with toluene to prepare starting solution. Precursor pyrolyzed at 500 °C for 240 min was finally annealed at 900–1200 °C for 240 min in Ar. X-ray diffraction analysis, field emission–scanning electron microscope and fluorescent spectrophotometer were used to evaluate structural and optical properties. For the 1000 °C-annealed powders with regular shape and narrow size distribution confirmed by FE–SEM observation, strong red emission at 615nm under the excitation of 395nm maximum was reached, then the higher annealed samples at above 1100 °C gave the lower emission intensities.

  3. Redox switching and oxygen evolution at hydrous oxyhydroxide modified nickel electrodes in aqueous alkaline solution: effect of hydrous oxide thickness and base concentration

    OpenAIRE

    Lyons, Michael

    2012-01-01

    Outstanding issues regarding the film formation, the redox switching reaction and the oxygen evolution reaction (OER) electrocatalytic behaviour of multi-cycled nickel oxy-hydroxide films in aqueous alkaline solution have been discussed. The oxide is grown using a repetitive potential multi-cycling technique, and the mechanism of the latter hydrous oxide formation process has been discussed. A duplex layer model of the oxide/solution interphase region is proposed. The acid/base behaviour of t...

  4. THERMODYNAMIC PROPERTIES OF NONAQUEOUS SINGLE SALT SOLUTIONS USING THE Q-ELECTROLATTICE EQUATION OF STATE

    Directory of Open Access Journals (Sweden)

    A. Zuber

    2015-09-01

    Full Text Available AbstractThe correlation of thermodynamic properties of nonaqueous electrolyte solutions is relevant to design and operation of many chemical processes, as in fertilizer production and the pharmaceutical industry. In this work, the Q-electrolattice equation of state (EOS is used to model vapor pressure, mean ionic activity coefficient, osmotic coefficient, and liquid density of sixteen methanol and ten ethanol solutions containing single strong 1:1 and 2:1 salts. The Q-electrolattice comprises the lattice-based Mattedi-Tavares-Castier (MTC EOS, the Born term and the explicit MSA term. The model requires two adjustable parameters per ion, namely the ionic diameter and the solvent-ion interaction energy. Predictions of osmotic coefficient at 298.15 K and liquid density at different temperatures are also presented.

  5. The sealing of excavation damaged zones in salt formations using sodium silicate solutions

    Energy Technology Data Exchange (ETDEWEB)

    Engelhardt, Hans-Joachim; Schmidt, Holger; Borstel, Lieselotte von [DBE TECHNOLOGY GmbH, Peine (Germany). Dept. of Repository Safety

    2015-07-01

    Since many decades, pressure grouting is an effective technique of civil engineering for sealing and stabilization purposes. Due to the potential contamination of fluids, grouting is of particular importance in repositories of radioactive waste. Traditional grouts for the sealing of fine fractures are sodium silicate solutions. Laboratory and field investigations prove that the particle-free solutions can be used to permanently seal excavation damaged zones (EDZ) in salt formations, because the solid reaction products are inert or almost insoluble. EDZ permeabilities of 10{sup -17} m{sup 2} can be achieved and were determined on the basis of the injection pressures and flow rates. High grouting pressures were realized as local test loadings. Laboratory tests show the fixation of Co{sup 2+}, Ni{sup 2+}, Sr{sup 2+}, Ba{sup 2+}, [UO{sub 2}]{sup 2+} and illustrate that sodium silicates may act additionally as a chemical barrier.

  6. The sealing of excavation damaged zones in salt formations using sodium silicate solutions

    International Nuclear Information System (INIS)

    Since many decades, pressure grouting is an effective technique of civil engineering for sealing and stabilization purposes. Due to the potential contamination of fluids, grouting is of particular importance in repositories of radioactive waste. Traditional grouts for the sealing of fine fractures are sodium silicate solutions. Laboratory and field investigations prove that the particle-free solutions can be used to permanently seal excavation damaged zones (EDZ) in salt formations, because the solid reaction products are inert or almost insoluble. EDZ permeabilities of 10-17 m2 can be achieved and were determined on the basis of the injection pressures and flow rates. High grouting pressures were realized as local test loadings. Laboratory tests show the fixation of Co2+, Ni2+, Sr2+, Ba2+, [UO2]2+ and illustrate that sodium silicates may act additionally as a chemical barrier.

  7. Preparation, stability, and structural characterization of plutonium(VII) in alkaline aqueous solution.

    Science.gov (United States)

    Antonio, Mark R; Williams, C W; Sullivan, James A; Skanthakumar, S; Hu, Yung-Jin; Soderholm, L

    2012-05-01

    A freshly prepared solution of Pu(VI) in 2 M NaOH was oxidized to Pu(VII), via ozonolysis, while simultaneously collecting X-ray absorption spectra. Analyses of the XANES (X-ray absorption near edge structure) and EXAFS (extended X-ray absorption fine structure) data, acquired throughout the in situ experiments, show a dioxo coordination environment for Pu(VI), PuO(2)(2+), typical for it and the hexavalent actinyl species of U and Np, and its evolution into a tetraoxo-coordination environment for Pu(VII), PuO(4)(-), like that known for Np(VII). The EXAFS data provide average Pu-O distances of 1.79(1) and 1.88(1) Å, respectively. The second coordination shells, also fit as O atoms, provide Pu-O distances of 2.29-2.32 Å that are independent of the Pu oxidation state. The coordination numbers for the distant O atoms in sums with those for the nearest O atoms are consistent with 6-O environments for both Pu(VI) and Pu(VII) ions in accordance with their previously proposed speciation as [Pu(VI)O(2)(OH)(4)](2-) and [Pu(VII)O(4)(OH)(2)](3-), respectively. This solution speciation accounts precisely for the Pu(VI) and Pu(VII) coordination environments reported in various solid state structures. The Pu(VII) tetraoxo-dihydroxo anion was found to have a half-life of 3.7 h. Its instability is attributed to spontaneous reduction to Pu(VI) and not to a measurable extent of disproportionation. We found no direct evidence for Pu(VIII) in the X-ray data and, furthermore, the stoichiometry of the oxidation of Cr(III) by Pu is consistent with that expected for a valence-pure Pu(VII) preparation by ozonation and, in turn, stoichiometrically equivalent to the established Np(VII)/Cr(III) redox reaction. PMID:22524489

  8. Evaluation of poly (aspartic acid sodium salt) as a draw solute for forward osmosis.

    Science.gov (United States)

    Gwak, Gimun; Jung, Bokyung; Han, Sungsoo; Hong, Seungkwan

    2015-09-01

    Poly (aspartic acid sodium salt) (PAspNa) was evaluated for its potential as a novel draw solute in forward osmosis (FO). The inherent advantages of PAspNa, such as good water solubility, high osmotic pressure, and nontoxicity, were first examined through a series of physicochemical analyses and atomic-scale molecular dynamics simulations. Then, lab-scale FO tests were performed to evaluate its suitability in practical processes. Compared to other conventional inorganic solutes, PAspNa showed comparable water flux but significantly lower reverse solute flux, demonstrating its suitability as a draw solute. Moreover, fouling experiments using synthetic wastewater as a feed solution demonstrated that PAspNa reversely flowed to the feed side reduced inorganic scaling on the membrane active layer. The recyclability of PAspNa was studied using both nanofiltration (NF) and membrane distillation (MD) processes, and the results exhibited its ease of recovery. This research reported the feasibility and applicability of FO-NF or FO-MD processes using PAspNa for wastewater reclamation and brackish water desalination. PMID:26005789

  9. Molecular Dynamics Studies of Concentrated Binary Aqueous Solutions of Lanthanide Salts: Structures and Exchange Dynamics

    International Nuclear Information System (INIS)

    Concentrated binary aqueous solutions of lanthanide (Nd3+ and Dy3+) salts (ClO4-, Cl-, and NO3-) have been studied by means of classical molecular dynamics (MD) simulations with explicit polarization and UV-visible spectroscopy. Pair interaction potentials, used for the MD simulations, have been developed in order to reproduce experimental hydration properties. Nd3+ and Dy3+ have been chosen because of their position in the lanthanide series: Nd3+ being a light lanthanide and Dy3+ a heavy one. They are respectively coordinated to nine and eight water molecules, in pure water, involving changes in their salt hydration structures. Both MD simulations and UV-visible experiments highlight the stronger affinity of nitrate anions toward Ln3+ compared to perchlorates and chlorides. Dissociation/association processes of Nd3+-Cl- and Nd3+-NO3- ion pairs in aqueous solution have been analyzed using potential of mean force profile calculations. Furthermore, from MD simulations, it appears that the affinity of anions (perchlorate, chloride, and nitrate. ) is stronger for Nd3+ than Dy3+. (authors)

  10. Characterization of Swollen States of Polyelectrolyte Brushes in Salt Solution by Neutron Reflectivity

    Energy Technology Data Exchange (ETDEWEB)

    Kobayashi, Motoyasu; Mitamura, Koji; Takahara, Atsushi [Institute for Materials Chemistry and Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395 (Japan); Terada, Masami [JST, ERATO (Japan); Yamada, Norifumi L, E-mail: takahara@cstf.kyushu-u.ac.jp [High Energy Accelerator Research Organization (KEK) (Japan)

    2011-01-01

    Cationic and zwitterionic polyelectrolyte brushes on quartz substrate were synthesized by surface-initiated atom transfer radical polymerization of 2-(methacryloyloxy)-ethyltrimethylammonium chloride (MTAC) and 2-(methacryloyloxy)ethyl phosphorylcholine (MPC). The effects of ionic strength on brush structure are investigated by neutron reflectivity (NR) in NaCl deuterium oxide (D{sub 2}O) solutions. We observed that poly(MTAC) chains were drastically shrunk at concentrations above 0.1 M NaCl/D{sub 2}O, which may be the change in charge-screening effect against ions on poly(MTAC). On the other hand, effect of salt concentration on a swollen state of poly(MPC) brush was negligible, even at the high concentration (5.0 M) close to saturation. The behaviour of poly(MPC) in salt aqueous solution is completely different from that of poly(MTAC), which may arise from the unique interaction properties, neutral nature, and hydrated water structure of phosphorylcholine units.

  11. Development of nano indium tin oxide (ITO) grains by alkaline hydrolysis of In(III) and Sn(IV) salts

    Indian Academy of Sciences (India)

    Nimai Chand Pramanik; Prasanta Kumar Biswas

    2002-11-01

    Indium tin oxide (ITO) nano powders of different compositions (In : Sn = 90 : 10, 70 : 30 and 50 : 50) were prepared by heat treatment (300–450°C) of mixed hydroxides of In(III) and Sn(IV). The hydroxides were obtained by the reaction of aq. NH3 with mixed aq. solutions of In(NO3)3 and SnCl4. FTIR and TG/DTA studies revealed that powders existed as In(OH)3 H2O−SnO3H2 H2O in the solid state and then they transformed to In2O3–SnO2 via some metastable intermediates after 300°C. Cubic phase of In2O3 was identified by XRD for the oxides up to 30% of Sn. Particle size measurements of the solid dispersed in acetone and SEM study for microstructure showed that the oxides were in the nano range (55–75 nm) whereas the size range determined from Debye–Scherrer equation were 11–24 nm.

  12. Pulse radiolysis study on tetra-alkylammonium hydroxides in alkaline solutions containing 02 and N20

    International Nuclear Information System (INIS)

    The reactivity of the oxide radical ion 0- and the decay kinetics of the ozonide ion, 03-, have been investigated in aqueous solutions at pH 12.8 in the presence of tetramethyl-, tetraethyl-, tetrapropyl-, and tetrabutylammonium ions, 02 and N20. Using pulse radiolysis to follow the 03- kinetics gives information on the competition of 02 and R4N+ for 0-. Absolute rate constants for these reactions are: 3.0 x 108 dm3 mol-1 s-1 for 0- + (CH3)4N+, 1.0 x 109 dm3 mol-1 s-1 for 0- + (C2H5)4N+, 1.3 x 109 dm3 mol-1 s-1 for 0- + (C3H7)4N+ and 2.2 x 109 dm3 mol-1 s-1 for O- + (C4H9)4N+. The decay of 03- occurs through the thermal dissociation reaction, 03 →(reversible) 02 + 0-, for which the absolute rate constant at 220C was found to be 6.2 +- 1.2 x 103 s-1. (author)

  13. Copper and brass aged at open circuit potential in slightly alkaline solutions

    International Nuclear Information System (INIS)

    Surface oxide films were grown on 99.99% copper and brass (copper-zinc alloy, Cu77Zn21Al2) in 0.1 mol L-1 borax solution at open circuit potential and were characterized using various experimental techniques. The composition of the passive films formed in situ on the different materials was studied using differential reflectance spectroscopy. The thickness of the oxide layers on copper and brass was compared by chronopotentiometric curves and potentiodynamic reductions. The electrical properties of each oxide were analyzed by means of electrochemical impedance spectroscopy. Their influence on the oxygen reduction reaction was also investigated using voltammetry hydrodynamic tools such as the rotating disk electrode. The results show that the incorporation of Zn to Cu in brass changes the composition and the thickness of the surface film. The films grown on brass tend to be thicker but less resistive and Zn compounds incorporate to the film. This is supported by results from reflectance and impedance spectroscopy. The kinetics of oxygen reduction is strongly inhibited on oxidized electrodes, particularly in the case of brass. The global number of exchanged electrons remains close to four and seems to be independent of the presence of surface oxides.

  14. Clastic dikes of the Hatrurim basin (western flank of the Dead Sea) as natural analogues of alkaline concretes: Mineralogy, solution chemistry, and durability

    Science.gov (United States)

    Sokol, E. V.; Gaskova, O. L.; Kozmenko, O. A.; Kokh, S. N.; Vapnik, E. A.; Novikova, S. A.; Nigmatulina, E. N.

    2014-11-01

    This study shows that the mineral assemblages from clastic dikes in areas adjacent to the Dead Sea graben may be considered as natural analogues of alkaline concretes. The main infilling material of the clastic dikes is composed of well-sorted and well-rounded quartz sand. The cement of these hard rocks contains hydroxylapophyllite, tacharanite, calcium silicate hydrates, opal, calcite, and zeolite-like phases, which is indicative of a similarity of the natural cementation processes and industrial alkaline concrete production from quartz sands and industrial alkaline cements. The quartz grains exhibit a variety of reaction textures reflecting the interaction with alkaline solutions (opal and calcium hydrosilicate overgrowths; full replacement with apophyllite or thomsonite + apophyllite). The physicochemical analysis and reconstruction of the chemical composition of peralkaline Ca, Na, and K solutions that formed these assemblages reveal that the solutions evolved toward a more stable composition of zeolite-like phases, which are more resistant to long-term chemical weathering and atmospheric corrosion. The 40Ar/39Ar age of 6.2 ± 0.7 Ma obtained for apophyllite provides conclusive evidence for the high corrosion resistance of the assemblages consisting of apophyllite and zeolite-like phases.

  15. A study on zeolite precipitation at alkaline conditions: effect of solution composition on mineralogy and crystallization rate

    International Nuclear Information System (INIS)

    Document available in extended abstract form only. Designs for engineered barrier systems for the geologic confinement of radioactive wastes involve the extensive use of bentonite, a material known for its capability to retard radionuclide migration into the groundwater system due to its low permeability. Cement and concrete are used in conjunction with bentonite to serve as structural supports and to seal access routes. However, when concrete becomes saturated with groundwater, it produces alkaline fluids that may attack and degrade the bentonite over time. A key concern regarding bentonite alteration by alkaline fluids is the precipitation of secondary minerals, such as zeolites, which may produce changes in the transport properties of the bentonite and compromise the stability of the entire barrier system. More importantly, studies have shown that zeolites form at timescales that are of interest in determining the long-term integrity of the barrier system. It is thus important to understand zeolite precipitation at conditions operative during bentonite alteration. The objective of this study, therefore, is to determine the effects of fluid composition on the crystallization rate and zeolite mineralogy. Zeolites were synthesized in batches from solutions with varying ratios of Si and Al at pH 13.5 by combining appropriate amounts of NaOH, NaAlO2 and Na2SiO3.9H2O. The Si and Al concentrations in the starting solutions both ranged from 0.03 to 0.24 M and the solution Si/Al ratios ranged from 0.125 to 8. The solutions were transferred to polypropylene bottles and stored in an oven set at a constant temperature of 70 deg. C for 1, 4, 7, 14 and 30 days. At appropriate reaction times, samples were extracted from the oven and then centrifuged to separate the solids from the liquid. The supernatant was filtered using 0.2 μm filter and the solids were washed several times before drying in a freeze dryer. The solids were characterized by XRD and SEM-EDX to determine the

  16. Electroreduction of oxygen on Vulcan carbon supported Pd nanoparticles and Pd-M nanoalloys in acid and alkaline solutions

    Energy Technology Data Exchange (ETDEWEB)

    Alexeyeva, N. [Institute of Chemistry, University of Tartu, Ravila 14A, 50411 Tartu (Estonia); Sarapuu, A., E-mail: ave.sarapuu@ut.ee [Institute of Chemistry, University of Tartu, Ravila 14A, 50411 Tartu (Estonia); Tammeveski, K. [Institute of Chemistry, University of Tartu, Ravila 14A, 50411 Tartu (Estonia); Vidal-Iglesias, F.J.; Solla-Gullon, J.; Feliu, J.M. [Instituto de Electroquimica, Universidad de Alicante, Apartado 99, 03080 Alicante (Spain)

    2011-07-30

    Highlights: > Electroreduction of O{sub 2} on carbon-supported Pd, PdCo and PdFe nanoparticles is studied. > Pd-based catalysts were prepared by reduction in the presence of citrate and in microemulsion. > Four-electron reduction of O{sub 2} proceeds in both acid and alkaline media. > Specific activity of PdCo and PdFe nanocatalysts was similar to that of Pd nanoparticles. - Abstract: The kinetics of O{sub 2} reduction on novel electrocatalyst materials deposited on carbon substrates were studied using the rotating disk electrode (RDE) technique. Palladium nanoparticles and Pd-M (PdCo and PdFe) nanoalloys supported on Vulcan XC-72R were prepared using two different synthetic routes. The catalyst samples were examined by transmission electron microscopy (TEM) and the average size of metal nanoparticles was determined. Electrochemical measurements were performed in 0.5 M H{sub 2}SO{sub 4} and in 0.1 M NaOH solutions. The influence of different synthetic conditions on the values of specific activity and other kinetic parameters was investigated. These parameters were determined from the Tafel plots taking into account the real electroactive area for each electrode. Pd nanoparticles and Pd-M nanoalloys exhibit significantly high electrocatalytic activity for the four-electron reduction of oxygen to water.

  17. Ultraviolet spectrum and decay of the ozonide ion radical, O/sub 3//sup -/, in strong alkaline solution. [Electron beams

    Energy Technology Data Exchange (ETDEWEB)

    Sehested, K.; Holcman, J.; Bjergbakke, E.; Hart, E.J.

    1982-05-27

    Pulse radiolytic experiments in strong alkaline solution (pH 13-14) on the formation and the decay of the ozonide ion radical, O/sub 3//sup -/, are reported. The high-pressure cell technique was used applying 4 MPa of nitrous oxide and 0.1 MPa of oxygen. The spectrum of O/sub 3//sup -/ in the uv was measured and the decay product was identified as the peroxy radical ion, O/sub 2//sup -/. A complete mechanism for the decay of O/sub 3//sup -/ is based on the following reactions: O/sub 3//sup -/ + O/sup -/ ..-->.. 2O/sub 2//sup -/ and O/sub 2//sup -/ + O/sup -/ + H/sub 2/O ..-->.. O/sub 2/ + 2OH/sup -/. A computer simulation of the high-pressure system as well as the atmospheric-pressure oxygenated system supports this mechanism and yields a rate constant, k/sub (O/sub 3//sup -/ + O/sup -/)/ of (7.0 +- 1.0) x 10/sup 8/ dm/sup 3/ mol/sup -1/s/sup -1/. As a consequence of our mechanism, a k/sub (O/sub 2//sup -/ + O/sup -/)/ of (6.0 +- 1.0) x 10/sup 8/ dm/sup 3/ mol/sup -1/ s/sup -1/ is also derived from the computations.

  18. Extraction of Zinc and Manganese from Alkaline and Zinc-Carbon Spent Batteries by Citric-Sulphuric Acid Solution

    Directory of Open Access Journals (Sweden)

    Francesco Ferella

    2010-01-01

    Full Text Available The paper is focused on the recovery of zinc and manganese from alkaline and zinc-carbon spent batteries. Metals are extracted by sulphuric acid leaching in the presence of citric acid as reducing agent. Leaching tests are carried out according to a 24 full factorial design, and empirical equations for Mn and Zn extraction yields are determined from experimental data as a function of pulp density, sulphuric acid concentration, temperature, and citric acid concentration. The highest values experimentally observed for extraction yields were 97% of manganese and 100% of zinc, under the following operating conditions: temperature 40∘C, pulp density 20%, sulphuric acid concentration 1.8 M, and citric acid 40 g L-1. A second series of leaching tests is also performed to derive other empirical models to predict zinc and manganese extraction. Precipitation tests, aimed both at investigating precipitation of zinc during leaching and at evaluating recovery options of zinc and manganese, show that a quantitative precipitation of zinc can be reached but a coprecipitation of nearly 30% of manganese also takes place. The achieved results allow to propose a battery recycling process based on a countercurrent reducing leaching by citric acid in sulphuric solution.

  19. The effect of nickel on alloy microstructure and electrochemical behaviour of AA1050 aluminium alloy in acid and alkaline solutions

    International Nuclear Information System (INIS)

    The study investigates the influence of nickel and magnesium additions to AA1050 aluminium alloy on the alloy electrochemical behaviour in sodium hydroxide and hydrochloric solutions under conditions relevant to industries that use alkaline etching as a standard surface treatment procedure and to the lithographic and electronic industries where surface convolution is assisted by pitting in hydrochloric acid. Scanning and transmission electron microscopes were used to characterize the intermetallic particles, and scanning Kelvin probe microscopy was utilised in monitoring the surface potential. Nickel is shown to be incorporated into second phase particles, which mostly consisted of Al3Fe and α-(AlFeSi) phases, resulting in enhanced cathodic activity on the aluminium surface. Consequently, the dissolution rates of the superpure aluminium, alloys without nickel addition and alloy with nickel addition are increased respectively in sodium hydroxide, and increased pitting is respectively promoted in hydrochloric acid. In contrast, the addition of magnesium to the alloy had negligible influence on the etching and pitting behaviour.

  20. Implications of alkaline solutions-induced etching on optical and minority carrier lifetime features of monocrystalline silicon

    Science.gov (United States)

    Bachtouli, N.; Aouida, S.; Laajimi, R. Hadj; Boujmil, M. F.; Bessais, B.

    2012-09-01

    In this work, we search to optimize the surface textures of monocrystalline silicon (c-Si) intended to be used in silicon solar cells. For this purpose, we studied the morphology of formed etch hillocks during anisotropic etching of silicon using alkaline solutions based on sodium hydroxide (NaOH), potassium hydroxide (KOH) and tetramethylammonium hydroxide (TMAH). Such treatments lead to the formation of various pyramids-like textures that can be well optimized to improve the photocurrent of c-Si-based solar cells. The produced textures were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), UV-visible optical reflectivity and minority carrier lifetime measurements. These investigations allow evaluating the size and density of the formed pyramidal textures; the apex angles vary between 75° and 82°, while the heights and bases of the pyramids range from a few hundred nanometers to several micrometers. A minimum reflectivity value of about 6% was obtained at specific conditions using NaOH, whereas it was found that the apparent effective minority carrier lifetime (τeff) is sensitive to the injection level (Δn), which shows an apparent increase from 1.2 μs to 2.4 μs for a minority carrier density of about Δn = 21014 cm-3.

  1. Hydrothermal crystallization and crystal growth of alpha-SiO /sub 2/ from rice husk silica ash in alkaline solution

    International Nuclear Information System (INIS)

    While pure and active amorphous silica was prepared from rice husk with 99.96% purity by acid leaching and pyrolysis. This silica could be crystallized into prismatic microcrystalline alpha-SiO/sub 2/ (77-88nm) under hydrothermal conditions (215 deg. C approx. equal to 20 atm. press) from alkaline solutions. The maximum yield of alpha-SiO/sub 2/ was obtained at 0.6 molar ratio of NaOH/SiO/sub 2/ which reduced to 0.2 in the presence of Al/sup 3+/ and /or B/sup 3+/ traces. This is due to formation of silicate crystals (considered to be a polymorph of SiO/sub 2/). It has been found that transition metal cations in the reaction media affects the degree of alpha-SiO/sub 2/ crystallization in the order: Fe/sup 3+/ > Ni/sup 2+/ > Cr/sup 3+/ > amorphous SiO/sub 2/ > Co/sup 2+/ > Cu/sup 2+/ > Mn/sup 2+/ > Zn/sup 2+/ > Zr/sup 2+/ > La/sup 3+/. Both mechanism of alpha-SiO/sub 2/ silicate growth and ions incorporation were discussed. (authors)

  2. Electromigration in molten salts and application to isotopic separation of alkaline and alkaline-earth elements; Electromigration en sels fondus et application a la separation des isotopes des elements alcalins et alcalino-terreux

    Energy Technology Data Exchange (ETDEWEB)

    Menes, F. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1969-07-01

    The separation of the isotopes of the alkaline-earth elements has been studied using counter-current electromigration in molten bromides. The conditions under which the cathode operates as a bromine electrode for the highest possible currents have been examined. For the separation of calcium, it has been necessary to use a stable CaBr{sub 2} - (CaBr{sub 2} + KBr) 'chain'. In the case of barium and strontium, it was possible to employ the pure bromides. Enrichment factors of the order of 10 for {sup 48}Ca and of the order of 1.5 for the rare isotopes of barium and strontium have been obtained. In the case of magnesium the method is slightly more difficult to apply because of material loss due to the relatively high vapour pressure of the salt requiring the use of electrolyte chains, MgBr{sub 2} - CeBr{sub 3}. A study has been made that has led to a larger-scale application of the method. These are essentially the inhibition of reversible operation of the cathode by traces of water, limiting the intensity which can be tolerated; evacuation of the heat produced by the Joule effect, in the absence of which the separation efficiency is reduced by thermal gradients; corrosion of the materials by molten salts at high temperature. Several cells capable of treating a few kilograms of substance have been put into operation; none of these has lasted long enough to produce a satisfactory enrichment. The method is thus limited actually to yields of the order of a few grams. (author) [French] On a etudie la separation des isotopes des elements alcalino-terreux par electromigration a contre-courant en bromures fondus. On a etudie les conditions dans lesquelles la cathode fonctionne en electrode a brome pour des intensites les plus elevees possibles. Pour la separation du calcium, il a ete necessaire d'utiliser une chaine stable CaBr{sub 2} - (CaBr{sub 2} + KBr). Pour le baryum et le strontium, on a pu operer sur les bromures purs. On a obtenu des facteurs d

  3. Investigation of the reaction of the ozonide ion with neptunium (VI) ions in aqueous alkaline solutions by the method of pulse radiolysis

    International Nuclear Information System (INIS)

    The method of pulse radiolysis with spectrophotometric recording of short-lived particles is used to investigate the kinetics of the reactions of O3- ion-radicals with Np(V) and Np(VI) in alkaline solutions. The rate constant of the first reaction is equal to (2.0 ± 0.3)·106, and of the second, (2.1 ± 0.2)·105 liter/(mole·sec) in 0.2-2.0 M LiOH. The peculiarities of γ-radiolysis of Np(VI) in alkaline solutions containing N2O and in aerated solutions containing K2S2O8 are elucidated. The yield of Np(VII) is determined by the behavior of O3-, which depends on the concentration of Np(VI) and OH-

  4. A fuel-cell reactor for the direct synthesis of hydrogen peroxide alkaline solutions from H(2) and O(2).

    Science.gov (United States)

    Yamanaka, Ichiro; Onisawa, Takeshi; Hashimoto, Toshikazu; Murayama, Toru

    2011-04-18

    The effects of the type of fuel-cell reactors (undivided or divided by cation- and anion-exchange membranes), alkaline electrolytes (LiOH, NaOH, KOH), vapor-grown carbon fiber (VGCF) cathode components (additives: none, activated carbon, Valcan XC72, Black Pearls 2000, Seast-6, and Ketjen Black), and the flow rates of anolyte (0, 1.5, 12 mL h(-1)) and catholyte (0, 12 mL h(-1)) on the formation of hydrogen peroxide were studied. A divided fuel-cell system, O(2) (g)|VGCF-XC72 cathode|2 M NaOH catholyte|cation-exchange membrane (Nafion-117)|Pt/XC72-VGCF anode|2 M NaOH anolyte at 12 mL h(-1) flow|H(2) (g), was effective for the selective formation of hydrogen peroxide, with 130 mA cm(-2) , a 2 M aqueous solution of H(2)O(2)/NaOH, and a current efficiency of 95 % at atmospheric pressure and 298 K. The current and formation rate gradually decreased over a long period of time. The cause of the slow decrease in electrocatalytic performance was revealed and the decrease was stopped by a flow of catholyte. Cyclic voltammetry studies at the VGCF-XC72 electrode indicated that fast diffusion of O(2) from the gas phase to the electrode, and quick desorption of hydrogen peroxide from the electrode to the electrolyte were essential for the efficient formation of solutions of H(2)O(2)/NaOH. PMID:21400665

  5. A New Composite Support for Pd Catalysts for Ethylene Glycol Electrooxidation in Alkaline Solution: Effect of (Ru,Sn)O2 solid solution

    International Nuclear Information System (INIS)

    Highlights: • Hydrothermal-prepared RuO2-SnO2 was added to XC-72 carbon black as composite support. • (Ru,Sn)O2 solid solution increases the EAS and specific activity of Pd. • (Ru,Sn)O2 changes the electron structure of Pd 3d and reduces CO coverage on Pd. • (Ru,Sn)O2 solid solution also enhances the OHads adsorption on Pd surface. • Pd/RuO2-SnO2/C catalyst shows highest activity and stability for EG oxidation. - Abstract: In this paper, RuO2-SnO2 binary oxides were prepared using a hydrothermal approach and added to Vulcan XC-72 carbon black as new support material for Pd. The X-ray diffraction, Transmission electron microscopy and X-ray photoelectronic spectra results show that the addition of binary oxides leads to the formation of (Ru,Sn)O2 solid solution in Pd/C catalyst and reduces the particle size of Pd particles due to the anchoring effect. In addition, the electrochemical CO-striping measurement reveals that the Pd/RuO2-SnO2/C catalyst exhibits the largest electrochemical active surface and the best CO tolerance. Moreover, cyclic voltammetry and chronoamperometry tests demonstrate that the Pd/RuO2-SnO2/C catalyst possesses a much higher specific activity (4.4 mA cm−2) than that of the Pd/C catalyst (3.2 mA cm−2) towards ethylene glycol electrooxidation in alkaline media, and better stability as well. These results support the suitability of Pd/RuO2-SnO2/C catalyst developed in this work as a promising candidate for direct alcohol fuel cells (DAFCs) application

  6. Conductivity and Viscosity Measurements for Binary Lysozyme Chloride Aqueous Solution and Ternary Lysozyme-Salt-Water Solution

    CERN Document Server

    Buzatu, D; Buzatu, F D

    2004-01-01

    We use the conductimetric method, adequate to electrolytes, to determine the lysozyme charge in lys-water and ternary lys-salt-water systems. We measured also the viscosities for the above binary and ternary systems in the same conditions at pH$=4.5$ and T$=298$ K, measurements that allow us to see any effect of viscosity on cations mobilities and implicitly on the lysozyme charge. The method is illustrated for the lysozyme chloride aqueous solution system at 25$^o$ C, using the data reported here for pH$=4.5$ at 0.15, 0.6, 0.8, 1., 1.5, 2., 2.5, 3., 3.5 mM (mg/mL) lysozyme chloride concentrations. The method was also applied to ternary lys-salt-water systems in the same conditions at pH$=4.5$ and T$=25^o$ C. Ternary conductivities are reported for a mean concentration 0.6 mM of lysozyme chloride in all systems and a mean concentration 0.01, 0.025, 0.05, 0.1, 0.175, 0.2, 0.5, 0.7, 0.9, 1.2, 1.3 and 1.4 M for NaCl; 0.005, 0.01, 0.05, 0.1, 0.175, 0.2, 0.5, 0.7, 0.9, 1.2, 1.3, 1.4 and 1.5 M for KCl; 0.005, 0.01,...

  7. KARAKTERISASI FISIKOKIMIA NANOKALSIUM HASIL EKSTRAKSI TULANG IKAN NILA MENGGUNAKAN LARUTAN BASA DAN ASAM [Physicochemical Characterization of Nano Calcium from Tilapia Bone Extracted by Alkaline and Acid Solution

    Directory of Open Access Journals (Sweden)

    Vanessa Lekahena*

    2014-06-01

    Full Text Available The utilization of tilapia (Oreochromis niloticus bones as a source of natural calcium was done by alkaline (NaOH and acid (HCl extraction. The extraction process aims to soften the bones are milled using disc mill into nano sized calcium powder or nanocalcium. The objective of this research was to study the physicochemical properties of nanocalcium obtained from alkaline and acid extraction of tilapia bones. The results of physicochemical analysis properties of nanocalcium sample showed that nanocalcium extracted by alkaline solution had better properties than that of the untreated sample and nanocalcium extracted by acid solution. The results was indicated by the higher yield, brighter colors, smaller particle size, and calcium content (20.67% and phosphorus (10.09% with a ratio of Ca/P = 2.0. The Fourier Transform Infrared (FTIR spectra profile indicated the presence of phosphate group (PO43- at the bands of 469, 563, 603, 961 and 1035 cm-1, and the presence of apatite carbonate group (CO32- was indicated by intense bands at 873, 1416, 1456 and 1563 cm-1. The morphology of the sampel surface of the alkaline extracted sample was smoother, denser, and the grain size formed were relatively larger. The formed crystalline phases were HAp (hydroxyapatite, carbonate apatite type A [Ca10(PO46CO3] and B [Ca10(PO43(CO33(OH2] with crystalline degree of 78.4%.

  8. The Influence of Calcium Chloride Salt Solution on the Transport Properties of Cementitious Materials

    Directory of Open Access Journals (Sweden)

    Yaghoob Farnam

    2015-01-01

    Full Text Available The chemical interaction between calcium chloride (CaCl2 and cementitious binder may alter the transport properties of concrete which are important in predicting the service life of infrastructure elements. This paper presents a series of fluid and gas transport measurements made on cementitious mortars before and after exposure to various solutions with concentrations ranging from 0% to 29.8% CaCl2 by mass. Fluid absorption, oxygen diffusivity, and oxygen permeability were measured on mortar samples prepared using Type I and Type V cements. Three primary factors influence the transport properties of mortar exposed to CaCl2: (1 changes in the degree of saturation, (2 calcium hydroxide leaching, and (3 formation of chemical reaction products (i.e., Friedel’s salt, Kuzel’s salt, and calcium oxychloride. It is shown that an increase in the degree of saturation decreases oxygen permeability. At lower concentrations (~12%, the formation of chemical reaction products (mainly calcium oxychloride is a dominant factor decreasing the fluid and gas transport in concrete.

  9. Hydrogen generation in microbial reverse-electrodialysis electrolysis cells using a heat-regenerated salt solution.

    Science.gov (United States)

    Nam, Joo-Youn; Cusick, Roland D; Kim, Younggy; Logan, Bruce E

    2012-05-01

    Hydrogen gas can be electrochemically produced in microbial reverse-electrodialysis electrolysis cells (MRECs) using current derived from organic matter and salinity-gradient energy such as river water and seawater solutions. Here, it is shown that ammonium bicarbonate salts, which can be regenerated using low-temperature waste heat, can also produce sufficient voltage for hydrogen gas generation in an MREC. The maximum hydrogen production rate was 1.6 m(3) H(2)/m(3)·d, with a hydrogen yield of 3.4 mol H(2)/mol acetate at a salinity ratio of infinite. Energy recovery was 10% based on total energy applied with an energy efficiency of 22% based on the consumed energy in the reactor. The cathode overpotential was dependent on the catholyte (sodium bicarbonate) concentration, but not the salinity ratio, indicating high catholyte conductivity was essential for maximizing hydrogen production rates. The direction of the HC and LC flows (co- or counter-current) did not affect performance in terms of hydrogen gas volume, production rates, or stack voltages. These results show that the MREC can be successfully operated using ammonium bicarbonate salts that can be regenerated using conventional distillation technologies and waste heat making the MREC a useful method for hydrogen gas production from wastes. PMID:22463373

  10. Hydrogen Generation in Microbial Reverse-Electrodialysis Electrolysis Cells Using a Heat-Regenerated Salt Solution

    KAUST Repository

    Nam, Joo-Youn

    2012-05-01

    Hydrogen gas can be electrochemically produced in microbial reverse-electrodialysis electrolysis cells (MRECs) using current derived from organic matter and salinity-gradient energy such as river water and seawater solutions. Here, it is shown that ammonium bicarbonate salts, which can be regenerated using low-temperature waste heat, can also produce sufficient voltage for hydrogen gas generation in an MREC. The maximum hydrogen production rate was 1.6 m3 H2/m3·d, with a hydrogen yield of 3.4 mol H2/mol acetate at a salinity ratio of infinite. Energy recovery was 10% based on total energy applied with an energy efficiency of 22% based on the consumed energy in the reactor. The cathode overpotential was dependent on the catholyte (sodium bicarbonate) concentration, but not the salinity ratio, indicating high catholyte conductivity was essential for maximizing hydrogen production rates. The direction of the HC and LC flows (co- or counter-current) did not affect performance in terms of hydrogen gas volume, production rates, or stack voltages. These results show that the MREC can be successfully operated using ammonium bicarbonate salts that can be regenerated using conventional distillation technologies and waste heat making the MREC a useful method for hydrogen gas production from wastes. © 2012 American Chemical Society.

  11. Results for the Fourth Quarter Calendar Year 2015 Tank 50H Salt Solution Sample

    International Nuclear Information System (INIS)

    In this memorandum, the chemical and radionuclide contaminant results from the Fourth Quarter Calendar Year 2015 (CY15) sample of Tank 50H salt solution are presented in tabulated form. The Fourth Quarter CY15 Tank 50H samples were obtained on October 29, 2015 and received at Savannah River National Laboratory (SRNL) on October 30, 2015. The information from this characterization will be used by Defense Waste Processing Facility (DWPF) & Saltstone Facility Engineering for the transfer of aqueous waste from Tank 50H to the Salt Feed Tank in the Saltstone Production Facility, where the waste will be treated and disposed of in the Saltstone Disposal Facility. This memorandum compares results, where applicable, to Saltstone Waste Acceptance Criteria (WAC) limits and targets. Data pertaining to the regulatory limits for Resource Conservation and Recovery Act (RCRA) metals will be documented at a later time per the Task Technical and Quality Assurance Plan (TTQAP) for the Tank 50H saltstone task. The chemical and radionuclide contaminant results from the characterization of the Fourth Quarter Calendar Year 2015 (CY15) sampling of Tank 50H were requested by SRR personnel and details of the testing are presented in the SRNL Task Technical and Quality Assurance Plan.

  12. Results for the Fourth Quarter Calendar Year 2015 Tank 50H Salt Solution Sample

    Energy Technology Data Exchange (ETDEWEB)

    Crawford, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-01-11

    In this memorandum, the chemical and radionuclide contaminant results from the Fourth Quarter Calendar Year 2015 (CY15) sample of Tank 50H salt solution are presented in tabulated form. The Fourth Quarter CY15 Tank 50H samples were obtained on October 29, 2015 and received at Savannah River National Laboratory (SRNL) on October 30, 2015. The information from this characterization will be used by Defense Waste Processing Facility (DWPF) & Saltstone Facility Engineering for the transfer of aqueous waste from Tank 50H to the Salt Feed Tank in the Saltstone Production Facility, where the waste will be treated and disposed of in the Saltstone Disposal Facility. This memorandum compares results, where applicable, to Saltstone Waste Acceptance Criteria (WAC) limits and targets. Data pertaining to the regulatory limits for Resource Conservation and Recovery Act (RCRA) metals will be documented at a later time per the Task Technical and Quality Assurance Plan (TTQAP) for the Tank 50H saltstone task. The chemical and radionuclide contaminant results from the characterization of the Fourth Quarter Calendar Year 2015 (CY15) sampling of Tank 50H were requested by SRR personnel and details of the testing are presented in the SRNL Task Technical and Quality Assurance Plan.

  13. Interaction of Nd(III) and Cm(III) with borate in dilute to concentrated alkaline NaCl, MgCl2 and CaCl2 solutions: solubility and TRLFS studies

    International Nuclear Information System (INIS)

    The interaction of lanthanides and trivalent actinides with borate in dilute to concentrated alkaline NaCl, MgCl2 and CaCl2 solutions was investigated at 22±2 C by a comprehensive series of solubility experiments with Nd(OH)3(am), and complemented with Cm(III)-TRLFS studies (TRLFS: time resolved laser fluorescence spectroscopy) under analogous pH and ionic strength conditions. Although there was clear evidence of borate complexation in the pH range of 8.5 to 10, overall no significant increase in Nd(III) solubility occurred in any of the investigated salt systems in the presence of [B](tot) ≤ 0.4 M, compared with analogous borate-free solutions. On the contrary, a significant decrease in Nd(III) concentration was observed at pHc ≤ 9 in NaCl and MgCl2 systems with [B](tot) ≥ 0.16 M (diluted salt systems) or [B](tot) ≥ 0.04 M (concentrated salt systems). This observation, together with a clear change in the slope of the solubility curve and the further confirmation by XPS analyses, indicates the transformation of Nd(OH)3(am) into a so far unknown Nd(III)-borate solid phase with significantly lower solubility. Similar Nd(III) concentrations in the aqueous phase are obtained in under-saturation solubility experiments conducted with a synthesized crystalline phase Nd[B9O13(OH)4](cr). TRLFS confirmed the formation of aqueous Cm(III)-borate complexes in dilute to concentrated NaCl and MgCl2 systems at pHc = 8 and [B](tot) ≥ 0.04 M. Two different Cm(III)-borate species are proposed based on the peak shift of the spectra, although the resulting fluorescence emission bands do not allow the definition of an unequivocal chemical model for this system. TRLFS also shows that no Cm(III)-borate complexes form under hyper-alkaline conditions (pHc = 12), due to the stronger competition posed by hydrolysis and the predominance of weakly coordinating B(OH)4- in the aqueous phase. These results show the impact of An(III)-borate interactions on An(III) speciation and

  14. Local chemical purification of vapor generators of supercritical pressure with inhibited solution of ammonium salt of ethylenediaminetetraacetic acid

    International Nuclear Information System (INIS)

    Inhibition of boiler steel corrosion by chemical cleaning of vapor generators by EDTC ammonium salt solutions was studied. The washing solution velocity was 1.5-2.0 m/s, EDTC ammonium salt concentration of 0.5-1.0 g/l, temperature of 150-170 deg C. The best inhibition was provided by M-1, MSDA inhibitors, ''composition 3'' and by OP-10 or OP-7 surfactants in concentrations of 0.05-0.06 g/l each. Advanced technology of local chemical cleaning is proposed

  15. Electrochemical quartz crystal microbalance study on Au-supported Pt adlayers for electrocatalytic oxidation of methanol in alkaline solution

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Underpotential deposition(UPD) of Cu on an Au electrode followed by redox replacement reaction(RRR) of CuUPD with a Pt source(H2PtCl6 or K2PtCl4) yielded Au-supported Pt adlayers(for short,Pt(CuUPD-Pt4+)n/Au for H2PtCl6,or Pt(CuUPD-Pt2+)n/Au for K2PtCl4,where n denotes the number of UPD-redox replacement cycles).The electrochemical quartz crystal microbalance(EQCM) technique was used for the first time to quantitatively study the fabricated electrodes and estimate their mass-normalized specific electrocatalytic activity(SECA) for methanol oxidation in alkaline solution.In comparison with Pt(CuUPD-Pt2+)n/Au,Pt(CuUPD-Pt4+)n/Au exhibited a higher electrocatalytic activity,and the maximum SECA was obtained to be as high as 35.7 mA ?g?1 at Pt(CuUPD-Pt4+)3/Au.The layer-by-layer architecture of Pt atoms on Au is briefly discussed based on the EQCM-revealed redox replacement efficiency,and the calculated distribution percentages of bare Au sites agree with the experimental results deduced from the charge under the AuOx-reduction peaks.The EQCM is highly recommended as an efficient technique to quantitatively examine various electrode-supported catalyst adlayers,and the highly efficient catalyst adlayers of noble metals are promising in electrocatalysis relevant to biological,energy and environmental sciences and technologies.

  16. An assessment of the long-term environmental impacts of reusing alkaline clay on coal refuse piles with a dynamic solute transport model at a watershed scale

    Science.gov (United States)

    Xu, Y.; Liang, X.; Davis, T. W.; Patterson, J.; Jaw, F. K.; Koranchie-Boah, P.

    2011-12-01

    Coal refuse piles play a significant role in producing acid mining drainage (AMD) that deteriorates water quality at a watershed scale. The waste produced from coal refuse piles results in a decrease of the pH value in soil water and river flow. Metal compounds, such as ferric and ferrous solutions, are also continuously released from the coal pile due to the extensive and complicated chemical reactions in the acidic environment. Alkaline clay, a byproduct of alumina refining process, has a high residual pH in the material. If the alkaline clay is used innovatively with the coal mine refuse, the problems associated with each (e.g., high and low pH values) are likely to be effectively resolved. In addition, the solubility of the sulfur and iron will be reduced significantly. This will effectively eliminate the AMD problem at the coal refuse pile and improve the water quality at the watershed scale. This study investigates the long-term impacts of the combined mixture (i.e., alkaline clay + coal refuse) on the environment (e.g., in the soil column and in the river system) through systematic modeling simulations in a combination with field measurements. In particular, a dynamic solute transport model that accounts for processes of the pyrite oxidation, oxygen diffusion, absorption, desorption, and advection is developed and is coupled with the Distributed Hydrology Soil and Vegetation Model (DHSVM) to assess the environmental impacts at the watershed scale. The model-simulated sulfur and iron concentrations are compared with field observations and the long-term impacts of the combined mixture (i.e., alkaline clay + coal refuse) on the environment are investigated. This study paves the way for monitoring and assessing the impacts of the reuse of the alkaline clay and refuse mixture on the environment at a watershed scale.

  17. Preparation of porous monolayer film by immersing the stearic acid Langmuir-Blodgett monolayer on mica in salt solution

    Energy Technology Data Exchange (ETDEWEB)

    Wang, S. [Institute of Near-Field Optics and Nano Technology, School of Physics and Optoelectronic Technology, Dalian University of Technology, Street No. 2 Linggong Road, Dalian 116024 (China); Li, Y.L.; Zhao, H.L.; Liang, H. [Institute of Photo-Biophysics, School of Physics and Electronic, Henan University, Jinming, Kaifeng 475004, Henan (China); Liu, B., E-mail: boliu@henu.edu.cn [Institute of Photo-Biophysics, School of Physics and Electronic, Henan University, Jinming, Kaifeng 475004, Henan (China); Pan, S., E-mail: span@dlut.edu.cn [Institute of Near-Field Optics and Nano Technology, School of Physics and Optoelectronic Technology, Dalian University of Technology, Street No. 2 Linggong Road, Dalian 116024 (China)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer Porous film has been prepared by immersing the stearic acid Langmuir-Blodgett monolayer on mica in salt solution. Black-Right-Pointing-Pointer The mechanism relies on the electrostatic screening effect of the cations in salt solution. Black-Right-Pointing-Pointer The factors influencing the size and area of the pores were investigated. - Abstract: Porous materials have drawn attention from scientists in many fields such as life sciences, catalysis and photonics since they can be used to induce some materials growth as expected. Especially, porous Langmuir-Blodgett (LB) film is an ideal material with controlled thickness and flat surface. In this paper, stearic acid (SA), which has been extensively explored in LB film technique, is chosen as the template material with known parameters to prepare the LB film, and then the porous SA monolayer film is obtained by means of etching in salt solution. The main etching mechanism is suggested that the cations in the solution block the electrostatic interaction between the polar carboxyl group of SA and the electronegative mica surface. The influencing factors (such as concentration of salt solution, valence of cation and surface pressure) of the porous SA film are systematically studied in this work. The novel method proposed in this paper makes it convenient to prepare porous monolayer film for designed material growth or cell culture.

  18. Preparation of porous monolayer film by immersing the stearic acid Langmuir–Blodgett monolayer on mica in salt solution

    International Nuclear Information System (INIS)

    Highlights: ► Porous film has been prepared by immersing the stearic acid Langmuir–Blodgett monolayer on mica in salt solution. ► The mechanism relies on the electrostatic screening effect of the cations in salt solution. ► The factors influencing the size and area of the pores were investigated. - Abstract: Porous materials have drawn attention from scientists in many fields such as life sciences, catalysis and photonics since they can be used to induce some materials growth as expected. Especially, porous Langmuir–Blodgett (LB) film is an ideal material with controlled thickness and flat surface. In this paper, stearic acid (SA), which has been extensively explored in LB film technique, is chosen as the template material with known parameters to prepare the LB film, and then the porous SA monolayer film is obtained by means of etching in salt solution. The main etching mechanism is suggested that the cations in the solution block the electrostatic interaction between the polar carboxyl group of SA and the electronegative mica surface. The influencing factors (such as concentration of salt solution, valence of cation and surface pressure) of the porous SA film are systematically studied in this work. The novel method proposed in this paper makes it convenient to prepare porous monolayer film for designed material growth or cell culture.

  19. Influence of acid and alkaline sources on optical, structural and photovoltaic properties of CdSe nanoparticles precipitated from aqueous solution

    Science.gov (United States)

    Coria-Monroy, C. Selene; Sotelo-Lerma, Mérida; Hu, Hailin

    2016-06-01

    CdSe is a widely researched material for photovoltaic applications. One of the most important parameters of the synthesis is the pH value, since it determines the kinetics and the mechanism of the reaction and in consequence, the optical and morphological properties of the products. We present the synthesis of CdSe in solution with strict control of pH and the comparison of ammonia and KOH as alkaline sources and diluted HCl as acid medium. CdSe formation was monitored with photoluminescence emission spectra (main peak in 490 nm, bandgap of CdSe nanoparticles). XRD patterns indicated that CdSe nanoparticles are mainly of cubic structure for ammonia and HCl, but the hexagonal planes appear with KOH. Product yield decreases with pH and also decreases with KOH at constant pH value since ammonia has a double function, as complexing agent and alkaline source. Changes in morphology were observed in SEM images as well with the different alkaline source. The effect of alkaline sources on photovoltaic performance of hybrid organic solar cells with CdSe and poly(3-hexylthiophene) as active layers was clearly observed, indicating the importance of synthesis conditions on optoelectronic properties of promising semiconductor nanomaterials for solar cell applications.

  20. Development of an analytical technique for the detection of alteration minerals formed in bentonite by reaction with alkaline solutions

    Science.gov (United States)

    Sakamoto, H.; Shibata, M.; Owada, H.; Kaneko, M.; Kuno, Y.; Asano, H.

    A multibarrier system consisting of cement-based backfill, structures and support materials, and a bentonite-based buffer material has been studied for the TRU waste disposal concept being developed in Japan, the aim being to restrict the migration of radionuclides. Concern regarding bentonite-based materials in this disposal environment relates to long-term alteration under hyper-alkaline conditions due to the presence of cementitious materials. In tests simulating the interaction between bentonite and cement, formation of secondary minerals due to alteration reactions under the conditions expected for geological disposal of TRU waste (equilibrated water with cement at low liquid/solid ratio) has not been observed, although alteration was observed under extremely hyper-alkaline conditions with high temperatures. This was considered to be due to the fact that analysis of C-S-H gel formed at the interface as a secondary mineral was difficult using XRD, because of its low crystallinity and low content. This paper describes an analytical technique for the characterization of C-S-H gel using a heavy liquid separation method which separates C-S-H gel from Kunigel V1 bentonite (bentonite produced in Japan) based on the difference in specific gravity between the crystalline minerals constituting Kunigel V1 and the secondary C-S-H gel. For development of C-S-H gel separation methods, simulated alteration samples were prepared by mixing 990 mg of unaltered Kunigel V1 and 10 mg of C-S-H gel synthesized using pure chemicals at a ratio of Ca/Si = 1.2. The simulated alteration samples were dispersed in bromoform-methanol mixtures with specific gravities ranging from 2.00 to 2.57 g/cm 3 and subjected to centrifuge separation to recover the light density fraction. Subsequent XRD analysis to identify the minerals was complemented by dissolution in 0.6 N hydrochloric acid to measure the Ca and Si contents. The primary peak (2 θ = 29.4°, Cu Kα) and secondary peaks (2 θ = 32.1

  1. Line emissions from sonoluminescence in aqueous solutions of halide salts without noble gases

    International Nuclear Information System (INIS)

    Line emissions of trivalent terbium (Tb3+) ion were observed from single-bubble sonoluminescence (SL) in an aqueous solution of terbium chloride (TbCl3) that contained no noble gas. In addition, sodium (Na) lines were observed in multi-bubble SL in aqueous solutions of various halide salts that contained no noble gas. These observations show that the halide ions, such as Cl−, Br−, and I−, help for line emissions as the noble gases. The intensity of a line emission depends on both the chemical species produced by cavitation bubbles and the temperature of SL bubble that responds to the driving ultrasound pressure. With the increase of driving pressure, some line emissions attached to the continuous spectrum may become increasingly clear, while other line emissions gradually become indistinct. - Highlights: • Line emissions of Tb(III) ions were observed without the presence of noble gases. • The halide ions help to generate a line emission during sonoluminescence. • The intensity of a line emission mainly depends on the bubble's temperature. • The definition of a line emission is related to the temperature of caviation bubble and the kind of host liquid

  2. Rubidium-87 NMR studies of rubidium salts and complexes with 18-crown-6 and cryptand-222 in solutions

    Science.gov (United States)

    Khazaeli, Sadegh; Dye, James L.; Popov, Alexander I.

    Rubidium-87 NMR measurements were used to study the behavior of the Rb + ion in water, methanol, and propylene carbonate solutions. In aqueous solutions the 87Rb chemical shift varies linearly with the mean activity of the salt. In methanol and propylene carbonate solutions the relationship is linear only at high salt concentrations. The resonance lines are broad and vary from ˜ 150 Hz (at half height) in water to ˜ 1000 Hz in propylene carbonate. Additions of macrocyclic ligands 18C6 and C222 to Rb + solutions in the three solvents result in further broadening of the resonance line so that variations in the resonance frequency cannot be measured with a reasonable precision.

  3. Formation of globules and aggregates of DNA chains in DNA/polyethylene glycol/monovalent salt aqueous solutions

    OpenAIRE

    Kawakita, H.; Uneyama, T.; Kojima, M; Morishima, K.; Masubuchi, Y.; Watanabe, H.(Max-Planck-Institut für Kernphysik, 69117, Heidelberg, Germany)

    2009-01-01

    It has been known that giant DNA shows structural transitions in aqueous solutions under the existence of counterions and other polymers. However, the mechanism of these transitions has not been fully understood. In this study, we directly observed structures of probed (dye-labeled), dilute DNA chains in unprobed DNA/polyethylene glycol (PEG)/monovalent salt (NaCl) aqueous solutions with fluorescent microscopy to examine this mechanism. Specifically, we varied the PEG molecular weight and sal...

  4. Secretion of an alkaline protease from a salt- tolerant and alkaliphilic, Streptomyces clavuligerus strain Mit-1 Secreção de uma protease alcalina por uma cepa halotolerante e alcalifílica de Streptomyces clavuligerus, Mit-1

    OpenAIRE

    Jignasha T. Thumar; Singh, Satya P.

    2007-01-01

    An alkaliphilic and salt- tolerant actinomycete, Streptomyces clavuligerus strain Mit-1, was isolated from Mithapur, the western coast of India. The organism was Gram-positive, having filamentous, long thread like structure. The sporulation started after two days of growth and the optimum level of alkaline protease (130 U/ml) was produced during the early stationary phase. The strain could grow and produce protease with 0-10% NaCl (w/v), the optimum being 5% NaCl (w/v). Growth and protease pr...

  5. The effects of polyethylene glycol (PEG) as an electrolyte additive on the corrosion behavior and electrochemical performances of pure aluminum in an alkaline zincate solution

    Energy Technology Data Exchange (ETDEWEB)

    Wang, X.Y. [Department of Chemistry, Zhejiang University, Hangzhou (China); Binzhou Medical College, Yantai (China); Wang, J.M.; Wang, Q.L.; Shao, H.B. [Department of Chemistry, Zhejiang University, Hangzhou (China); Zhang, J.Q. [Department of Chemistry, Zhejiang University, Hangzhou (China); State Key Laboratory for Corrosion and Protection of Metal, Institute of Metal Research, Chinese Academy of Sciences, Shenyang (China)

    2011-12-15

    The effects of zinc oxide and/or polyethylene glycol (PEG) as electrolyte additives on the corrosion and electrochemical performances of pure aluminum in 4.0 M KOH solutions were investigated by means of hydrogen collection, polarization curve, galvanostatic discharge, scanning electron microscopy (SEM), and energy dispersive analysis of X-ray (EDAX). The addition of ZnO markedly inhibited the corrosion of aluminum in 4.0 M KOH solutions, resulting from the deposition of zinc with high hydrogen evolution overpotential in aluminum surfaces. The introduction of PEG in the alkaline zincate solution obviously improved the deposition of zinc by increase in the overpotential of zinc deposition, thus the corrosion rate of aluminum in the alkaline zincate solutions with PEG was further decreased. The enhancement effect of PEG on the inhibition of zinc oxide first increased and then decreased with increasing the content of PEG in the electrolyte. The electrolyte system with 0.2 M ZnO and 2.0 mM PEG presented the highest inhibition efficiency (98.8%) for the corrosion of aluminum. The results of galvanostatic discharge indicated that the aluminum anode shows excellent discharge performances in the 4.0 M KOH solution with 0.2 M ZnO and 2.0 mM PEG. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  6. The electrochemical behaviour of 2205 duplex stainless steel in alkaline solutions with different pH in the presence of chloride

    International Nuclear Information System (INIS)

    Highlights: ► The pH plays important roles in 2205 DSS passive film composition and occurrence of pitting. ► The passive film of 2205 DSS in the alkaline solution, presenting a bilayer structure, composed of an outer and inner layer. ► As the pH increases, there is a gradual enrichment in chromium and nitrogen in the surface film. ► The peak of NH3/NH4+ is disappeared in the pH 10.5 solutions. ► The pit initiated at inclusions or in austenite phase near the γ/δ boundaries. - Abstract: The electrochemical behaviour of 2205 duplex stainless steel in alkaline solutions with different pH values in the presence of NaCl was evaluated by different techniques: potentiodynamic measurements, electrochemical impedance spectroscopy and capacitance measurements (Mott–Schottky approach). The chemical composition was studied by X-ray photoelectron spectroscopy (XPS). In addition, the site of pitting nucleated preferentially on the duplex stainless steel had been confirmed by scanning electron microscopy (SEM). The results indicated that both the pH and immersion time play important roles in the evolution of the film resistance, charge transfer processes and the occurrence of pitting. The composition of the surface film changes with the pH value. The film formed in the alkaline solution, presenting a bilayer structure, predominantly contained Fe species and Cr-oxide. The NH3/NH4+ species in the passive film are disappeared in the pH 10.5 solution. The pit initiation sites occurred in austenite phase near the γ/δ boundaries or at inclusions. The number and size of the pits increases with the decrease of pH value after long time immersion.

  7. Characterization of the deviation to the ideality of concentrated actinide and lanthanide salt solutions: contribution of the Bimsa theory

    International Nuclear Information System (INIS)

    The aim of this work is to describe the mean stoichiometric activity coefficients, osmotic coefficients or water activities of aqueous actinide nitrate salt solutions up to high concentration. These sets of data are required for a better control of the equilibria occurring in liquid-liquid extraction processes. Experimental acquisition of these thermodynamic properties, in the case of some actinide nitrates, is possible and was conducted before.But, many actinide salt solutions cannot be experimentally handled up to high concentration because of unstable oxidation state or very high radioactivity. As a consequence, a suitable predictive theory is necessary for the description of these nitrate salt solutions (such as Am (NO3)3, Cm (NO3)3). The BIMSA ('Binding Mean Spherical Approximation') was chosen for this purpose. This theory, unlike other methods, uses a set of microscopic parameters that have some physical meaning, for the description of macroscopic thermodynamic properties (osmotic coefficients, activity coefficients).The following manuscript is divided by 4 chapters, corresponding to 4 articles accepted in the scientific journal 'Journal of Physical Chemistry'. Chapter 1 first reviews the basic thermodynamic concepts before describing the issues involved in acquiring actinides binary data. An approach based on the thermodynamic concept of simple solutions, the notion of fictive binary data, is described. Within this approach, the activity coefficient of an aqueous phase constituent depends on two parameters: the water activity of the system and total concentration of dissolved constituents. As a first application, new fictive binary data of uranyl nitrate are proposed from measurements on the ternary system UO2(NO3)2/HNO3/H2O.Chapter 2 gives the main principles of the BIMSA theory. It shows also preliminary promising results obtained when modeling lanthanide(III) salt properties. Then, in chapter 3, two predictive capabilities of the theory are shown. One of

  8. Fundamental Properties of Salts

    Energy Technology Data Exchange (ETDEWEB)

    Toni Y Gutknecht; Guy L Fredrickson

    2012-11-01

    Thermal properties of molten salt systems are of interest to electrorefining operations, pertaining to both the Fuel Cycle Research & Development Program (FCR&D) and Spent Fuel Treatment Mission, currently being pursued by the Department of Energy (DOE). The phase stability of molten salts in an electrorefiner may be adversely impacted by the build-up of fission products in the electrolyte. Potential situations that need to be avoided, during electrorefining operations, include (i) fissile elements build up in the salt that might approach the criticality limits specified for the vessel, (ii) electrolyte freezing at the operating temperature of the electrorefiner due to changes in the liquidus temperature, and (iii) phase separation (non-homogenous solution). The stability (and homogeneity) of the phases can be monitored by studying the thermal characteristics of the molten salts as a function of impurity concentration. Simulated salt compositions consisting of the selected rare earth and alkaline earth chlorides, with a eutectic mixture of LiCl-KCl as the carrier electrolyte, were studied to determine the melting points (thermal characteristics) using a Differential Scanning Calorimeter (DSC). The experimental data were used to model the liquidus temperature. On the basis of the this data, it became possible to predict a spent fuel treatment processing scenario under which electrorefining could no longer be performed as a result of increasing liquidus temperatures of the electrolyte.

  9. Geobacter sp. SD-1 with enhanced electrochemical activity in high-salt concentration solutions.

    Science.gov (United States)

    Sun, Dan; Call, Douglas; Wang, Aijie; Cheng, Shaoan; Logan, Bruce E

    2014-12-01

    An isolate, designated strain SD-1, was obtained from a biofilm dominated by Geobacter sulfurreducens in a microbial fuel cell. The electrochemical activity of strain SD-1 was compared with type strains, G. sulfurreducens PCA and Geobacter metallireducens GS-15, and a mixed culture in microbial electrolysis cells. SD-1 produced a maximum current density of 290 ± 29 A m−3 in a high-concentration phosphate buffer solution (PBS-H, 200 mM). This current density was significantly higher than that produced by the mixed culture (189 ± 44 A m−3) or the type strains (NaCl), current by SD-1 (158 ± 4 A m−3) was reduced by 28% compared with 50 mM PBS (220 ± 4 A m−3), but it was still higher than that of the mixed culture (147 ± 19 A m−3), and strains PCA and GS-15 did not produce any current. Electrochemical tests showed that the improved performance of SD-1 was due to its lower charge transfer resistance and more negative potentials produced at higher current densities. These results show that the electrochemical activity of SD-1 was significantly different than other Geobacter strains and mixed cultures in terms of its salt tolerance. PMID:25756125

  10. Salting-out of methane in the aqueous solutions of urea and sarcosine

    Indian Academy of Sciences (India)

    M K Dixit; Anupam Chatterjee; B L Tembe

    2016-04-01

    Hydrophobic association and solvation of methane molecules in aqueous solutions of urea and sarcosine (sa) have been studied using MD simulations. The potentials of mean force (PMFs) between methane molecules in water, water-sa, water-urea and water-urea-sa mixtures show an enhancement of methane association on the addition of these osmolytes. These observations are well supported by calculation of equilibrium constants. Calculation of thermodynamic parameters shows that the association of methane is stabilized by entropy and favored by enthalpy. The hydrophobic solvation of methane is stabilized by enthalpy and destabilized by entropy. The calculated solvation free energies of methane in these mixtures show that methane is less soluble in the mixtures of urea and sarcosine than in water. The solubility is the least in the water-urea-sa mixture. Analysis of distributions of solvent and co-solvent around methane suggests that the local densities of both urea and sarcosine are diminished around the methane in the mixtures of these osmolytes. The selective reduction of both urea and sarcosine from methane surface suggests that both urea and sarcosine push methane molecules towards water and increase the interaction between methane molecules i.e., salting-out of methane.

  11. G eobacter sp. SD-1 with enhanced electrochemical activity in high-salt concentration solutions

    KAUST Repository

    Sun, Dan

    2014-07-16

    © 2014 Society for Applied Microbiology and John Wiley & Sons Ltd. Summary: An isolate, designated strain SD-1, was obtained from a biofilm dominated by Geobacter sulfurreducens in a microbial fuel cell. The electrochemical activity of strain SD-1 was compared with type strains, G.sulfurreducensPCA and Geobacter metallireducensGS-15, and a mixed culture in microbial electrolysis cells. SD-1 produced a maximum current density of 290±29Am-3 in a high-concentration phosphate buffer solution (PBS-H, 200mM). This current density was significantly higher than that produced by the mixed culture (189±44Am-3) or the type strains (<70Am-3). In a highly saline water (SW; 50mM PBS and 650mM NaCl), current by SD-1 (158±4Am-3) was reduced by 28% compared with 50mM PBS (220±4Am-3), but it was still higher than that of the mixed culture (147±19Am-3), and strains PCA and GS-15 did not produce any current. Electrochemical tests showed that the improved performance of SD-1 was due to its lower charge transfer resistance and more negative potentials produced at higher current densities. These results show that the electrochemical activity of SD-1 was significantly different than other Geobacter strains and mixed cultures in terms of its salt tolerance.

  12. Experimental study of natural convection melting of ice in salt solutions

    International Nuclear Information System (INIS)

    The solid-liquid interface morphology and the micro-physical process near the moving phase boundary during natural convection melting of a horizontal layer of ice by an overlying pool of salt solution were studied experimentally. A cathetometer which amplifies the interface region was used to measure the ice melting rate. Also measured were the temperature transients of the liquid pool. Within the temperature and the density ratio ranges explored, the ice melting rate was found to be very sensitive to the ratio of pool-to-ice melt density but independent of pool-to-ice temperature difference. By varying the density ratio, three different flow regimes and morphologies of the solid-liquid interface were observed, with melt streamers emanating from the crests of the wavy interface into the pool in all three cases. The measured wavelengths (spacing) between the streamers for four different pairs of materials were correlated with the density ratio and found to agree favorably with the predictions of Taylor instability theory

  13. In vitro corrosion of ZEK100 plates in Hank's Balanced Salt Solution

    Directory of Open Access Journals (Sweden)

    Waizy Hazibullah

    2012-03-01

    Full Text Available Abstract Background In recent years magnesium alloys have been intensively investigated as potential resorbable materials with appropriate mechanical and corrosion properties. Particularly in orthopedic research magnesium is interesting because of its mechanical properties close to those of natural bone, the prevention of both stress shielding and removal of the implant after surgery. Methods ZEK100 plates were examined in this in vitro study with Hank's Balanced Salt Solution under physiological conditions with a constant laminar flow rate. After 14, 28 and 42 days of immersion the ZEK100 plates were mechanically tested via four point bending test. The surfaces of the immersed specimens were characterized by SEM, EDX and XRD. Results The four point bending test displayed an increased bending strength after 6 weeks immersion compared to the 2 week group and 4 week group. The characterization of the surface revealed the presence of high amounts of O, P and Ca on the surface and small Mg content. This indicates the precipitation of calcium phosphates with low solubility on the surface of the ZEK100 plates. Conclusions The results of the present in vitro study indicate that ZEK100 is a potential candidate for degradable orthopedic implants. Further investigations are needed to examine the degradation behavior.

  14. Rate of Post-traumatic Endophthalmitis with or without Injection of Balanced Salt Solution

    Directory of Open Access Journals (Sweden)

    Nasrin Rafati

    2013-01-01

    Full Text Available Purpose: In a study complementing a previous multicenter randomized clinical trial on prophylactic injection of intraocular antibiotics during primary repair of penetrating eye injuries (PEIs, we sought to determine whether needle entrance and injection of balanced salt solution (BSS, per se, could increase the rate of acute post-traumatic bacterial endophthalmitis (APBE. Methods: Patients randomized to the BSS injection arm (n=167 of the Traumatic Endophthalmitis Trial, and eligible patients who had refused enrollment and received no intraocular injections during primary repair (n=111 were compared for the development of APBE. Results: APBE occurred in 8 of 167 (4.8% eyes in the BSS group and in 5 of 111 (4.5% eyes in the non-injection group (P=0.91. Retained intraocular foreign bodies were present in 46 eyes including 25 (15% eyes in the BSS injection group and 21 (18.9% eyes in the non-injection group (P=0.38. Logistic regression analysis showed no significant difference between BSS injected and non-injected eyes in terms of APBE (P=0.69. However, the presence of intraocular foreign bodies was strongly associated with the risk of endophthalmitis (P<0.001, OR=14.1, 95% CI: 4.1-48.5. Conclusion: Needle entrance and intraocular injection of BSS during primary repair of PEIs does not increase the risk of APBE.

  15. SANS from Salt-Free Aqueous Solutions of Hydrophilic and Highly Charged Star-Branched Polyelectrolytes

    Directory of Open Access Journals (Sweden)

    François Boué

    2016-06-01

    Full Text Available Scattering functions of sodium sulfonated polystyrene (NaPSS star-branched polyelectrolytes with high sulfonation degrees were measured from their salt-free aqueous solutions, using the Small Angle Neutron Scattering (SANS technique. Whatever the concentration c, they display two maxima. The first, of abscissa q1*, is related to a position order between star cores and scales as q1* ∝ c1/3. The second, of abscissa q2*, is also observed in the scattering function of a semi-dilute solution of NaPSS linear polyelectrolytes. In the dilute regime (c < c*, non-overlapping stars, peak abscissa does not depend on concentration c and is just an intramolecular characteristic associated with the electrostatic repulsion between arms of the same star. In the semi-dilute regime, due to the star interpenetration, the scattering function – through the peak position, reflects repulsion between arms of the same star or of different stars. The c threshold between these distinct c-dependencies of q2* in the dilute and semi-dilute regimes is estimated as c*. Just as simple is the measurement of the geometrical radius R of the star obtained from the q1* value at c* through the relation 2R = 2π/q1*. By considering NaPSS stars of the same functionality with different degrees of polymerization per arm Na, we find R scaling linearly with Na, suggesting an elongated average conformation of the arms. This is in agreement with theoretical predictions and simulations. Meanwhile the value of q2* measured in the dilute regime does not allow any inhomogeneous counterion distribution inside the stars to be revealed.

  16. Physico-Chemical Study of the Separation of Calcium Isotopes by Chemical Exchange Between Amalgam and Salt Solutions

    International Nuclear Information System (INIS)

    In a preliminary study of the isotopic exchange between Ca amalgam and aqueous or organic solutions of Ca salts, the main parameters governing the feasibility of a separation process based on these systems such as separation factor, exchange kinetics, rate of decomposition of the amalgam were investigated. The separation factor between 40Ca and 46Ca was found to be of the order of 1.02. The rate of the exchange reaction is rather low for aqueous solutions, extremely low for organic solutions. The amalgam seems not to be attacked by dimethyl-formamide solutions; but it is rapidly decomposed by aqueous solutions of Ca halides. This decomposition is slow in the case of aqueous solutions of calcium formate and still slower for Ca(OH)2; however, except in particular conditions, the observed rate is often much higher, owing to interfering reactions between amalgam and water vapor contained in H2 bubbles. (authors)

  17. Structure of a model salt bridge in solution investigated with 2D-​IR spectroscopy

    NARCIS (Netherlands)

    A. Huerta-Viga; S.R. Domingos; S. Amirjalayer; S. Woutersen

    2013-01-01

    Salt bridges are known to be important for the stability of protein conformation, but up to now it has been difficult to study their geometry in soln. Here we characterize the spatial structure of a model salt bridge between guanidinium (Gdm+) and acetate (Ac-​) using two-​dimensional vibrational (2

  18. Electronic Tongue for Qualitative Analysis of Aqueous Solutions of Salts Using Thick-film Technology and Metal Electrodes

    Directory of Open Access Journals (Sweden)

    Juan Soto

    2006-09-01

    Full Text Available An electronic tongue for the qualitative analysis of aqueous solutions of salts hasbeen developed. The following set of electrodes was used: RuO2, Ag, and Cu in thick-filmtechnology and Au, Pb, Zn and Ni as small bars of the corresponding metal. The response ofthe designed “electronic tongue” was tested on a family of samples containing pure salt andcomplex mixtures. The electrodes were used as potentiometric un-specific sensors and thee.m.f. of each electrode in contact with a certain aqueous solution was used as input signalfor a PCA analysis. The study showed that the set of electrodes were capable to discriminatebetween aqueous solutions of salts basically by their different content in anions and cations(the anions SO42-, Cl-, PO4H2-, CO3H-, NO3- and cations Na+ and K+ were studied. In orderto better analyze the basis for the discrimination power shown by the electronic tongue, aquantitative analysis was also envisaged. A fair estimation of the concentrations of thedifferent ions in the solutions studied appeared to be possible using this electronic tonguedesign.Keywords:

  19. Characterization and precipitation mechanism of α-calcium sulfate hemihydrate growing out of FGD gypsum in salt solution

    Institute of Scientific and Technical Information of China (English)

    YANG LiuChun; GUAN BaoHong; WU ZhongBiao

    2009-01-01

    Alpha-calcium sulfate hemihydrate (α-HH) has been prepared from flue gas desulfurization (FGD)gypsum with salt solution method under atmospheric pressure. X-ray diffraction (XRD), thermogra-vimetry and differential scanning calorimetry (TG-DSC), optical micrograph, X-ray photoelectron spec-troscopy (XPS), energy dispersive spectrometry (EDS), and scanning electron microscopy (SEM) have been employed to characterize the α-HH crystals, based on which the formation and growth mecha-nisms of the a-HH crystals have been discussed. The results show that FGD gypsum can be success-fully transformed into high purity α-HH in salt solution under mild conditions, and that a dissolu-tion-recrystallization route is most probably adopted by this transition. The growth of a-HH crystals in salt solution demonstrates a preferred direction along [001] and results in a bundle-of-sheets or bun-dle-of-raphide texture. The characteristics revealed in this study can help to understand and control the growth of the α-HH crystal from solution.

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

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2016-05-01

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

  1. Fast separation of DNA sequencing fragments in highly alkaline solutions of linear polyacrylamide using electrophoresis in bare silica capillaries

    Czech Academy of Sciences Publication Activity Database

    Klepárník, Karel; Malá, Zdeňka; Boček, Petr

    2001-01-01

    Roč. 22, č. 4 (2001), s. 783-788. ISSN 0173-0835 R&D Projects: GA ČR GA203/00/0772; GA ČR GA303/00/0928; GA AV ČR IAA4031703 Institutional research plan: CEZ:AV0Z4031919 Keywords : capillary electrophoresis * alkaline environment * bare capillary Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 4.282, year: 2001

  2. Extraction of Zinc and Manganese from Alkaline and Zinc-Carbon Spent Batteries by Citric-Sulphuric Acid Solution

    OpenAIRE

    Francesco Ferella; Ida De Michelis; Francesca Beolchini; Valentina Innocenzi; Francesco Vegliò

    2010-01-01

    The paper is focused on the recovery of zinc and manganese from alkaline and zinc-carbon spent batteries. Metals are extracted by sulphuric acid leaching in the presence of citric acid as reducing agent. Leaching tests are carried out according to a 24 full factorial design, and empirical equations for Mn and Zn extraction yields are determined from experimental data as a function of pulp density, sulphuric acid concentration, temperature, and citric acid concentration. The highest values exp...

  3. Electrocatalytic oxidation of ethanol on various metal ad-layer modified Au(111) electrodes in alkaline solution

    OpenAIRE

    DURSUN, Zekerya; KARABİBEROĞLU, Şükriye ULUBAY; GELMEZ, Buket

    2011-01-01

    Ethanol oxidation was studied on single-crystal Au(111) electrodes that were modified by platinum, palladium, and cadmium metal ad-layers. The metal ad-layer modification was carried out by the underpotential deposition process, in which controlled amounts of Pt, Pd, and Cd were electrodeposited onto the substrate as submonolayer or monolayer coverage. The activity of the metal ad-layer modified Au(111) electrodes toward ethanol oxidation was studied in alkaline media, and recorded v...

  4. Chain dimensions in free and immobilized brush states of polysulfobetaine in aqueous solution at various salt concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Terayama, Y; Arita, H; Ishikawa, T; Takahara, A [Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0385 (Japan); Kikuchi, M; Mitamura, K; Kobayashi, M [JST, ERATO Takahara Soft Interfaces Project, 744 Motooka, Nishi-ku, Fukuoka 819-0385 (Japan); Yamada, N L, E-mail: takahara@cstf.kyushu-u.ac.jp [Neutron Science Laboratory, High Energy Accelerator Research Organization, 1-1 Oho, Tsukuba, Ibaraki 305-0801 (Japan)

    2011-01-01

    The chain dimensions of free and immobilized polysulfobetaine in aqueous solution at various salt concentrations were investigated by size-exclusion chromatography with multiangle light scattering and neutron reflectivity measurement, respectively. The dependence of the z-average mean square radius of gyration ({sub z}{sup 1/2}) on the weight-average molecular weight (M{sub w}) of free poly(3-(N-2-methacryloyloxyethyl-N,N-dimethyl)ammonatopropanesulfo-nate) (MAPS) in aqueous solution at salt concentrations of 74, 100, 200, and 500 mM was described by the perturbed wormlike chain model using the chain stiffness parameter {lambda}{sup -1} the molar mass per unit contour length ML, and the excluded volume effect B. B increased from 0 to 1.8 nm with increasing salt concentration to 500 mM due to the screening of attractive electrostatic interaction between ammonium cations and sulfonyl anions by salt ions. The swollen structure of the poly(MAPS) brush in D{sub 2}O changed from a shrunken state to a relatively extended state with increasing salt concentration from 0 to 500 mM NaCl/D{sub 2}O solution. The thickness of the swollen poly(MAPS) brush in 500 mM NaCl/D{sub 2}O was 9.0 times greater than 2{sub z}{sup 1/2} of free poly(MAPS) due to high osmotic pressure generated by the excluded volume effect of densely grafted polymer chains.

  5. Acid and salt uptake during the marinatig process of Engraulis anchoita fillets influence of the solution: fish ratio and agitation

    Directory of Open Access Journals (Sweden)

    María Eugenia Capaccioni

    2011-12-01

    Full Text Available The aims of this research were to determine the effect of different conditions of the marination stage on the salt and acid uptake, immersion time, and sensorial characteristics during the marinating process of anchovy (Engraulis anchoita. Different solution:fish ratios and the agitation effect during this stage were analyzed. The ratios used were: 0.77:1, 3:1 and 10:1 (with and without agitation. An increase of marinating solution:fish ratio causes a higher speed of acid and salt penetration The product obtained with the 10:1 ratio had a dry and fibrous texture and a slightly salty taste. Salt concentration was statistically significantly lower (p < 0.01 in the samples with agitation. Agitation did not influence the acid uptake, and the salt penetration speed decreased, but rancidity was detected in this product. The ratio 3:1 decreases the marinating time without damaging sensory attributes and can be used in the fish marinating process.

  6. Formation of ozone in the reaction between the ozonide radical ion, O3-, and the carbonate radical ion, CO3-, in aqueous alkaline solutions

    International Nuclear Information System (INIS)

    Ozone forms in aqueous alkaline solutions by a reaction between the O3- and CO3- radical ions. This reaction has been demonstrated under conditions favorable for the generation of suitable concentrations of these ions by a high-pressure pulse radiolysis technique. The reaction is O3- + CO3- → O3 + CO32-. Its rate constant k/sub (O3-+CO3-)/ of (6 +- 2) x 107 dm3 mol-1 s-1 has been determined by computer simulation of the reactions involved

  7. Electrochemical activation of carbon cloth in aqueous inorganic salt solution for superior capacitive performance

    Science.gov (United States)

    Ye, Dong; Yu, Yao; Tang, Jie; Liu, Lin; Wu, Yue

    2016-05-01

    Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as an electrode material for flexible supercapacitors. However, pristine CC has such a low surface area and poor electrochemical activity that the energy storage capability is usually very poor. Herein, we report a green method, two-step electrochemical activation in an aqueous solution of inorganic salts, to significantly enhance the capacitance of CC for supercapacitor application. Micro-cracks, exfoliated carbon fiber shells, and oxygen-containing functional groups (OFGs) were introduced onto the surface of the carbon filament. This resulted in an enhancement of over two orders of magnitude in capacitance compared to that of the bare CC electrode, reaching up to a maximum areal capacitance of 505.5 mF cm-2 at the current density of 6 mA cm-2 in aqueous H2SO4 electrolyte. Electrochemical reduction of CC electrodes led to the removal of most electrochemically unstable surface OFGs, resulting in superior charging/discharging rate capability and excellent cycling stability. Although the activated CC electrode contained a high-level of surface oxygen functional groups (~15 at%), it still exhibited a remarkable charging-discharging rate capability, retaining ~88% of the capacitance when the charging rate increased from 6 to 48 mA cm-2. Moreover, the activated CC electrode exhibited excellent cycling stability with ~97% capacitance remaining after 10 000 cycles at a current density of 24 mA cm-2. A symmetrical supercapacitor based on the activated CC exhibited an ideal capacitive behavior and fast charge-discharge properties. Such a simple, environment-friendly, and cost-effective strategy to activate CC shows great potential in the fabrication of high-performance flexible supercapacitors.Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as

  8. Investigation into aqueous solutions of lanthanum (3) and scandium (3) salts using 139La and 45Sc NMR method

    International Nuclear Information System (INIS)

    139La and 45Sc NMR method has been used to study composition and structure of lanthanum (3) and scandium (3) coordination sphere in aqueous solutions in respect to concentration of dissolved salt and nature of (NO3-, Cl-, ClO4-) anion. Lanthanum and scandium are shown to form intraspherical complexes both with nitrate- and with perchlorate anions. Chloride-ion able to complexing with Sc3+ ions in aqueous solutions coordinates to La3+ ions only in solutions with large excess of Cl- anions (Cl-:La3+ > 17.6 at lanthanum (3) concentration equal to 0.40 g-ion/l). Equilibrium between aquocomplexes with different coordination number N-nine and eight is stated to exist in aqueous solutions of lanthanum chloride, octaaquolanthanum (3) prevailing in concentrated solutions

  9. Electrochemical activation of carbon cloth in aqueous inorganic salt solution for superior capacitive performance.

    Science.gov (United States)

    Ye, Dong; Yu, Yao; Tang, Jie; Liu, Lin; Wu, Yue

    2016-05-21

    Carbon cloth (CC) is an inexpensive and highly conductive textile with excellent mechanical flexibility and strength; it holds great promise as an electrode material for flexible supercapacitors. However, pristine CC has such a low surface area and poor electrochemical activity that the energy storage capability is usually very poor. Herein, we report a green method, two-step electrochemical activation in an aqueous solution of inorganic salts, to significantly enhance the capacitance of CC for supercapacitor application. Micro-cracks, exfoliated carbon fiber shells, and oxygen-containing functional groups (OFGs) were introduced onto the surface of the carbon filament. This resulted in an enhancement of over two orders of magnitude in capacitance compared to that of the bare CC electrode, reaching up to a maximum areal capacitance of 505.5 mF cm(-2) at the current density of 6 mA cm(-2) in aqueous H2SO4 electrolyte. Electrochemical reduction of CC electrodes led to the removal of most electrochemically unstable surface OFGs, resulting in superior charging/discharging rate capability and excellent cycling stability. Although the activated CC electrode contained a high-level of surface oxygen functional groups (∼15 at%), it still exhibited a remarkable charging-discharging rate capability, retaining ∼88% of the capacitance when the charging rate increased from 6 to 48 mA cm(-2). Moreover, the activated CC electrode exhibited excellent cycling stability with ∼97% capacitance remaining after 10 000 cycles at a current density of 24 mA cm(-2). A symmetrical supercapacitor based on the activated CC exhibited an ideal capacitive behavior and fast charge-discharge properties. Such a simple, environment-friendly, and cost-effective strategy to activate CC shows great potential in the fabrication of high-performance flexible supercapacitors. PMID:27141910

  10. Prediction of corrosion rate of AZ31B magnesium alloy under salt fog environment in NaCl solution

    OpenAIRE

    even">D.Thirumalaikumarasamy,; , K.Shanmugam and V. Balasubramanian

    2013-01-01

    Magnesium alloys have gained considerable interest as a material for automotive and aerospace applications due to its low density, high specific strength, and good castability. However, another considerable issue is their corrosion properties. This restricts their practical applications. In this present research, corrosion behavior of the AZ31B magnesium alloy was evaluated by conducting salt fog test in NaCl solution at different chloride ion concentrations, pH values, spraying times, and ai...

  11. Ageing behaviour of unary hydroxides in trivalent metal salt solutions: Formation of layered double hydroxide (LDH)-like phases

    Indian Academy of Sciences (India)

    Michael Rajamathi; P Vishnu Kamath

    2000-10-01

    The hydroxides of Mg, Ni, Cu and Zn transform into layered double hydroxide (LDH)-like phases on ageing in solutions of Al or Cr salts. This reaction is similar to acid leaching and proceeds by a dissolution–reprecipitation mechanism offering a simple method of LDH synthesis, with implications for the accepted theories of formation of LDH minerals in the earth’s crust.

  12. Modeling of Flow, Transport and Controlled Sedimentation Phenomena during Mixing of Salt Solutions in Complex Porous Formations

    Science.gov (United States)

    Skouras, Eugene D.; Jaho, Sofia; Pavlakou, Efstathia I.; Sygouni, Varvara; Petsi, Anastasia; Paraskeva, Christakis A.

    2015-04-01

    The deposition of salts in porous media is a major engineering phenomenon encountered in a plethora of industrial and environmental applications where in some cases is desirable and in other not (oil production, geothermal systems, soil stabilization etc). Systematic approach of these problems requires knowledge of the key mechanisms of precipitating salts within the porous structures, in order to develop new methods to control the process. In this work, the development and the solution of spatiotemporally variable mass balances during salt solution mixing along specific pores were performed. Both analytical models and finite differences CFD models were applied for the study of flow and transport with simultaneous homogeneous and heterogeneous nucleation (by crystal growth on the surface of the pores) in simple geometries, while unstructured finite elements and meshless methods were developed and implemented for spatial discretization, reconstruction, and solution of transport equations and homogeneous / heterogeneous reactions in more complex geometries. At initial stages of this work, critical problem parameters were identified, such as the characteristics of the porosity, the number of dissolved components, etc. The parameters were then used for solving problems which correspond to available experimental data. For each combination of ions and materials, specific data and process characteristics were included: (a) crystal kinetics (nucleation, growth rates or reaction surface rates of crystals, critical suspension concentrations), (b) physico-chemical properties (bulk density, dimensions of generated crystals, ion diffusion coefficients in the solution), (c) operating parameters (macroscopic velocity, flow, or pressure gradient of the solution, ion concentration) (d) microfluidic data (geometry, flow area), (e) porosity data in Darcy description (initial porosity, specific surface area, tortuosity). During the modeling of flow and transport in three

  13. Thermodynamics of binding water and solute to powdered long-chain salts of fatty acids.

    Science.gov (United States)

    Mahapatra, P K; Chattoraj, D K

    1994-10-01

    Hydration of powdered fatty acids and their salts has been studied both in presence and absence of neutral salts, sucrose and urea using the isopiestic vapour pressure technique. Moles of water vapour adsorbed per mole or kg of soaps like sodium palmitate, sodium stearate, sodium myristate and sodium laurate have been measured in presence and absence of salts and compared with that of detergents (SDS, CTAB, DTAB and MTAB). For each case of positive excess adsorption of water vapour and negative excess adsorption of inorganic salts, urea and sucrose to different soaps, the standard free energy change (delta G degrees) per kg of substrate in bringing the bulk mole fraction from zero to unity have been calculated using an appropriate thermodynamic equation and the values so obtained have been compared critically. PMID:7851944

  14. Electrochemical processing of alkaline nitrate and nitrite wastes

    International Nuclear Information System (INIS)

    Processing of high-level waste at the Savannah River Plant (SRP) will produce, as a by-product, a low-level, alkaline salt solution containing approximately 17% sodium nitrate and sodium nitrite. This solution will be incorporated into a cement formulation, saltstone, and placed in an engineered landfill. Electrochemical methods have been investigated to decrease the nitrate and nitrite in this solution in order to lower the leaching of nitrate and nitrite from saltstone and to reduce the volume of saltstone. Laboratory experiments have demonstrated the technical feasibility of electrolytically reducing the nitrate and nitrite in a synthetic salt solution similar in composition to that expected to be produced at SRP. Greater than 99% of the sodium nitrate and sodium nitrite can be reduced, producing ammonia, nitrogen, oxygen, and sodium hydroxide. In addition, significant reductions in the volume of saltstone may be realized if the sodium hydroxide produced by electrolysis can be recycled

  15. Glyoxal and methylglyoxal Setschenow salting constants in sulfate, nitrate, and chloride solutions

    DEFF Research Database (Denmark)

    Waxman, Eleanor M.; Elm, Jonas; Kurtén, Theo;

    2015-01-01

    .06 molality(-1)). We show that KS values for different salts are additive and present an equation for use in atmospheric models. Additionally, we have performed a series of quantum chemical calculations to determine the interactions between glyoxal/methylglyoxal monohydrate with Cl(-), NO3(-), SO4(2-), Na......(-), and Cl(-) modify partitioning, while cations do not. Other factors such as ion charge or partitioning volume effects likely need to be considered to fully explain salting effects....

  16. Soft X-ray absorption spectra of aqueous salt solutions with highly charged cations in liquid microjets

    Energy Technology Data Exchange (ETDEWEB)

    Schwartz, Craig P.; Uejio, Janel S.; Duffin, Andrew M.; Drisdell, Walter S.; Smith, Jared D.; Saykally, Richard J.

    2010-03-11

    X-ray absorption spectra of 1M aqueous solutions of indium (III) chloride, yttrium (III) bromide, lanthanum (III) chloride, tin (IV) chloride and chromium (III) chloride have been measured at the oxygen K-edge. Relatively minor changes are observed in the spectra compared to that of pure water. SnCl{sub 4} and CrCl{sub 3} exhibit a new onset feature which is attributed to formation of hydroxide or other complex molecules in the solution. At higher energy, only relatively minor, but salt-specific changes in the spectra occur. The small magnitude of the observed spectral changes is ascribed to offsetting perturbations by the cations and anions.

  17. An elastic rod model to evaluate effects of ionic concentration on equilibrium configuration of DNA in salt solution

    OpenAIRE

    Xiao, Ye; huang, Zaixing; Wang, Shengnan

    2014-01-01

    As a coarse-gained model, a super-thin elastic rod subjected to interfacial interactions is used to investigate the condensation of DNA in a multivalent salt solution. The interfacial traction between the rod and the solution environment is determined in terms of the Young–Laplace equation. Kirchhoff’s theory of elastic rod is used to analyze the equilibrium configuration of a DNA chain under the action of the interfacial traction. Two models are established to characterize the change of the ...

  18. Rheological and kinetic study of the ultrasonic degradation of locust bean gum in aqueous saline and salt-free solutions.

    Science.gov (United States)

    Li, Ruoshi; Feke, Donald L

    2015-11-01

    The ultrasonic degradation of locust bean gum (LBG) in aqueous solutions has been studied at 25°C for ultrasonication times up to 120 min. Although LBG is not a polyelectrolyte, the degradation extent and kinetics were found to be somewhat sensitive to the ionic conditions in solution, and this is attributed to changes in molecular conformation that can occur in different salt environments. Ultrasonic degradation was tracked by rheological measurements that lead to the determination of intrinsic viscosity for the LBG molecules. A kinetic model was also developed and successfully applied to characterize and predict the degradation results. PMID:26186852

  19. Chloride-inducible transient apoplastic alkalinizations induce stomata closure by controlling abscisic acid distribution between leaf apoplast and guard cells in salt-stressed Vicia faba.

    Science.gov (United States)

    Geilfus, Christoph-Martin; Mithöfer, Axel; Ludwig-Müller, Jutta; Zörb, Christian; Muehling, Karl H

    2015-11-01

    Chloride stress causes the leaf apoplast transiently to alkalize, an event that is presumed to contribute to the ability of plants to adapt to saline conditions. However, the initiation of coordinated processes downstream of the alkalinization is unknown. We hypothesize that chloride-inducible pH dynamics are a key chemical feature modulating the compartmental distribution of abscisic acid (ABA) and, as a consequence, affecting stomata aperture. Apoplastic pH and stomata aperture dynamics in intact Vicia faba leaves were monitored by microscopy-based ratio imaging and porometric measurements of stomatal conductance. ABA concentrations in leaf apoplast and guard cells were compared with pH dynamics by gas-chromatography-mass-spectrometry (GC-MS) and liquid-chromatography-tandem-mass spectrometry (LC-MS/MS). Results demonstrate that, upon chloride addition to roots, an alkalizing factor that initiates the pH dynamic propagates from root to leaf in a way similar to xylem-distributed water. In leaves, it induces a systemic transient apoplastic alkalinization that causes apoplastic ABA concentration to increase, followed by an elevation of endogenous guard cell ABA. We conclude that the transient alkalinization, which is a remote effect of chloride stress, modulates the compartmental distribution of ABA between the leaf apoplast and the guard cells and, in this way, is instrumental in inducing stomata closure during the beginning of salinity. PMID:26096890

  20. The electrochemical behaviour of stainless steel AISI 304 in alkaline solutions with different pH in the presence of chlorides

    International Nuclear Information System (INIS)

    Highlights: → The passivation and passivation breakdown of AISI 304 in alkaline solutions with different pH was studied. → The electrochemical behaviour and the corrosion resistance in chloride environments were evaluated using d.c. potentiodynamic polarization and electrochemical impedance spectroscopy. → The results were modelled using a hierarchically distributed circuit and revealed a more susceptible surface at pH 9. → The passive film characterization was carried out by SEM and EDS analysis, revealing the existence of MnS inclusions and the increase of Cr/Fe ratio in the attacked areas, preferably the vicinity of those inclusions. - Abstract: Nowadays, stainless steel reinforcements appear as an effective solution to increase the durability of reinforced concrete structures exposed to very aggressive environments. AISI 304 is widely used for this purpose. Although the improved durability of reinforcing AISI 304, when compared to carbon steel, there is a high probability of pitting susceptibility in the presence of chlorides. Thus, the present work aims at studying the passivation and passivation breakdown of AISI 304 in alkaline solutions of different pH (pH from 13 to 9), simulating the interstitial concrete electrolyte. These solutions were contaminated with different concentrations of chloride ions (3% and 10%, as NaCl). The electrochemical behaviour was evaluated by d.c. potentiodynamic polarization and by electrochemical impedance spectroscopy (EIS). The morphological features and the changes observed in the surface composition were evaluated by Scanning Electron Microscopy (SEM) together with EDS chemical analysis. The results evidence that pH plays an important role in the evolution of the film resistance and charge transfer processes. Moreover, the effect is highly dependent upon the chloride content and immersion time.

  1. Distributions of 14 elements on 63 absorbers from three simulant solutions (acid-dissolved sludge, acidified supernate, and alkaline supernate) for Hanford HLW Tank 102-SY

    International Nuclear Information System (INIS)

    As part of the Hanford Tank Waste Remediation System program at Los Alamos, we evaluated 63 commercially available or experimental absorber materials for their ability to remove hazardous components from high-level waste (HLW). These absorbers included cation and anion exchange resins, inorganic exchangers, composite absorbers, and a series of liquid extractants sorbed on porous support-beads. We tested these absorbers with three solutions prepared to simulate acid-dissolved sludge (pH 0.6), acidified supernate (pH 3.5), and alkaline supernate (pH 13.9) from underground storage tank 102-SY at the Hanford Reservation near Richland, Washington. To these simulants we added the appropriate radionuclides and used gamma spectrometry to measure fission products (Ce, Cs, Sr, Tc, and Y), actinides (U, Pu, and Am), and matrix elements (Cr, Co, Fe, Mn, Zn, and Zr). For each of more than 2500 element/absorber/solution combinations, we measured distribution coefficients for dynamic contact periods of 30 min, 2 h, and 6 h to obtain information about sorption kinetics. Because we measured the sorption of many different elements, the tabulated results indicate those elements most likely to interfere with the sorption of elements of greater interest. On the basis of nearly 7500 measured distribution coefficients, we determined that many of these absorbers appear suitable for processing HLW. This study supersedes the previous version of LA-12654, in which results attributed to a solution identified as an alkaline supernate simulant were misleading because that solution contained insufficient hydroxide

  2. The effects of surface treatment and stannate as an electrolyte additive on the corrosion and electrochemical performances of pure aluminum in an alkaline methanol-water solution

    Energy Technology Data Exchange (ETDEWEB)

    Zeng, X.X. [Department of Chemistry, Zhejiang University, Zheda Road 38, Hangzhou 310027, Zhejiang (China); Wang, J.M., E-mail: wjm@zju.edu.cn [Department of Chemistry, Zhejiang University, Zheda Road 38, Hangzhou 310027, Zhejiang (China); Wang, Q.L.; Kong, D.S.; Shao, H.B. [Department of Chemistry, Zhejiang University, Zheda Road 38, Hangzhou 310027, Zhejiang (China); Zhang, J.Q.; Cao, C.N. [Department of Chemistry, Zhejiang University, Zheda Road 38, Hangzhou 310027, Zhejiang (China); State Key Laboratory for Corrosion and Protection of Metal, Institute of Metal Research, Chinese Academy of Sciences, 62 Wencui Road, Shenyang 110016 (China)

    2010-06-01

    Pure aluminum electrodes were treated in alkaline stannate solutions, and the effects of some factors such as NaOH content and treating time were explored. The corrosion and electrochemical performances of the modified aluminum anodes in 4.0 M KOH methanol-water mixed solutions containing a methanol/water volume ratio of 7:3 (30% water) with and without stannate were investigated by means of hydrogen collection, polarization curve, galvanostatic discharge, scanning electron microscopy (SEM), and energy dispersive analysis of X-ray (EDAX). Metallic tin with high hydrogen evolution overpotential was deposited in aluminum surfaces by the modification treatments using stannate, resulting in the relatively low corrosion rate and markedly enhanced discharge performance of the modified aluminum anodes. In our experimental range the aluminum electrode treated in the solution with 0.1 M NaOH for 30 min showed lower corrosion rate and better discharge performance. The addition of Na{sub 2}SnO{sub 3} in 4.0 M KOH methanol-water mixed solutions with 30% water inhibited the corrosion of the aluminum electrodes modified in the treating solution with 0.1 M NaOH for 30 min, resulting from the deposition of tin with high hydrogen evolution overpotential in aluminum surfaces. The deposition of metallic tin on the electrode surface and the existence of stannate in the electrolytes were responsible for the notable enhancement in the discharge performance of the modified aluminum anode.

  3. Salting the landscapes in Transbaikalia: natural and technogenic factors

    Science.gov (United States)

    Peryazeva, E. G.; Plyusnin, A. M.; Chinavlev, A. M.

    2010-05-01

    Salting the soils, surface and subsurface waters is widespread in Transbaikalia. Hearths of salting occur within intermountain depressions of the Mesozoic and Cenozoic age both in the steppe arid and forest humid landscapes. Total water mineralization reaches 80 g/dm3 in lakes and 4-5 g/dm3 in subsurface waters. The waters belong to hydrocarbonate sodium and sulfate sodium types by chemical composition. The soda type of waters is widely spread through the whole area. Sulfate waters are found in several hearths of salting. Deposition of salts takes place in some lakes. Mirabilite and soda depositions are most commonly observed in muds of salt lakes. Deposition of salts occurs both as a result of evaporative concentrating and during freezing out the solvent. In the winter period, efflorescences of salts, where decawater soda is main mineral, are observed on ice surface. Solonchaks are spread in areas of shallow ground waters (1-2m). Soil salting is most intense in the lower parts of depressions, where surface of ground waters is at depth 0.5-1.0m. In soil cover of solonchaks, salt horizon is of various thicknesses, and it has various morphological forms of occurrence, i.e. as thick deposits of salts on soil surface and salting the surficial horizons. The soil has low alkaline reaction of medium and is characterized by high content of exchangeable bases with significant content of exchangeable sodium in the absorbing complex. Total amount of salts varies from 0.7 to 1.3%. Their maximal quantity (3.1%) is confined to the surficial layer. Sulfate-sodium type of salting is noted in the solonchak upper horizons and sulfate-magnesium-calcium one in the lower ones (Ubugunov et al, 2009). Formation of salting hearths is associated with natural and technogenic conditions. The Mesozoic depressions of Transbaikalia are characterized by intense volcanism. Covers of alkaline and moderately alkaline basalts that are enriched in potassium, sodium, carbon dioxide, fluorine, chlorine

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

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2015-09-14

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

  5. Self-consistent field theory investigation of the behavior of hyaluronic acid chains in aqueous salt solutions

    Science.gov (United States)

    Nogovitsin, E. A.; Budkov, Yu. A.

    2012-04-01

    In this work we continue to develop a field-theoretic methodology, which combines the technique of Gaussian equivalent representation for the calculation of functional integrals with the continuous Gaussian thread model of flexible polymers for solving statistical-mechanical problems of polyelectrolyte solutions. We present new analytic expressions for the osmotic pressure, the potential of mean force, and the monomer-monomer pair distribution function, and employ them to investigate the structural and thermodynamic quantities of the polyelectrolyte system. We demonstrate the applicability of the method for systems of polyelectrolyte chains in which the monomers interact via a Yukawa-type pair potential. As a specific example, the present work focuses on aqueous solutions of hyaluronic acid with added salts NaCl and CaCl2. Hyaluronic acid is a high molecular weight linear polysaccharide, which has a multitude of roles in biological tissues. We conclude that the effect of sodium chloride and calcium chloride on the osmotic properties of hyaluronic acid solutions can be accounted for by their contributions to the ionic strength. Nevertheless, the effects of coiling and self-association can be stimulated in solution by added salt.

  6. On the appearance of vorticity and gradient shear bands in wormlike micellar solutions of different CPCl/salt systems

    Energy Technology Data Exchange (ETDEWEB)

    Mütze, Annekathrin, E-mail: muetzea@ethz.ch; Heunemann, Peggy; Fischer, Peter [ETH Zürich, Institute of Food, Nutrition and Health, Schmelzbergstrasse 9, 8092 Zürich (Switzerland)

    2014-11-01

    Wormlike micellar salt/surfactant solutions (X-salicylate, cetylpyridinium chloride) are studied with respect to the applied shear stress, concentration, temperature, and composition of the counterions (X = lithium, sodium, potassium, magnesium, and calcium) of the salicylate salt solute to determine vorticity and gradient shear bands. A combination of rheological measurements, laser technique, video analysis, and rheo-small-angle neutron scattering allow for a detailed exploration of number and types of shear bands. Typical flow curves of the solutions show Newtonian, shear-thinning, and shear-thickening flow behavior. In the shear-thickening regime, the solutions show vorticity and gradient shear bands simultaneously, in which vorticity shear bands dominate the visual effect, while gradient shear bands always coexist and predominate the rheological response. It is shown that gradient shear bands change their phases (turbid, clear) with the same frequency as the shear rate oscillates, whereas vorticity shear bands change their phases with half the frequency of the shear rate. Furthermore, we show that with increasing molecular mass of the counterions the number of gradient shear bands increases, while the number of vorticity shear bands remains constant. The variation of temperature, shear stress, concentration, and counterions results in a predictable change in the rheological behavior and therefore allows adjustment of the number of vorticity shear bands in the shear band regime.

  7. Bathing in a magnesium-rich Dead Sea salt solution improves skin barrier function, enhances skin hydration, and reduces inflammation in atopic dry skin.

    Science.gov (United States)

    Proksch, Ehrhardt; Nissen, Hans-Peter; Bremgartner, Markus; Urquhart, Colin

    2005-02-01

    Magnesium salts, the prevalent minerals in Dead Sea water, are known to exhibit favorable effects in inflammatory diseases. We examined the efficacy of bathing atopic subjects in a salt rich in magnesium chloride from deep layers of the Dead Sea (Mavena(R) Dermaline Mg(46) Dead Sea salt, Mavena AG, Belp, Switzerland). Volunteers with atopic dry skin submerged one forearm for 15 min in a bath solution containing 5% Dead Sea salt. The second arm was submerged in tap water as control. Before the study and at weeks 1-6, transepidermal water loss (TEWL), skin hydration, skin roughness, and skin redness were determined. We found one subgroup with a normal and one subgroup with an elevated TEWL before the study. Bathing in the Dead Sea salt solution significantly improved skin barrier function compared with the tap water-treated control forearm in the subgroup with elevated basal TEWL. Skin hydration was enhanced on the forearm treated with the Dead Sea salt in each group, which means the treatment moisturized the skin. Skin roughness and redness of the skin as a marker for inflammation were significantly reduced after bathing in the salt solution. This demonstrates that bathing in the salt solution was well tolerated, improved skin barrier function, enhanced stratum corneum hydration, and reduced skin roughness and inflammation. We suggest that the favorable effects of bathing in the Dead Sea salt solution are most likely related to the high magnesium content. Magnesium salts are known to bind water, influence epidermal proliferation and differentiation, and enhance permeability barrier repair. PMID:15689218

  8. Mössbauer spectroscopic studies of frozen aqueous solutions of Fe3+ salts

    DEFF Research Database (Denmark)

    Mørup, Steen; Knudsen, J. E.; Nielsen, M. K.; Trumpy, Georg

    1976-01-01

    attributed to changes in the average separation between the iron ions. In the FeCl3–H2O system, it was found that homogeneous glasses are easily formed when the salt concentration is larger than 3.5 moles FeCl3 per 100 moles H2O. In more dilute samples, ice crystallizes during cooling, while the salt...... glass forming agents such as NO3 - , ClO4 - , and glycerol are also discussed. In some systems it was found that the states obtained after cooling depend critically on the cooling rate. The Journal of Chemical Physics is copyrighted by The American Institute of Physics....

  9. Effect of initial pH and temperature of iron salt solutions on formation of magnetite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gnanaprakash, G. [Metallurgy and Materials Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India); Mahadevan, S. [Metallurgy and Materials Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India); Jayakumar, T. [Metallurgy and Materials Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India); Kalyanasundaram, P. [Metallurgy and Materials Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India); Philip, John [Metallurgy and Materials Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India)]. E-mail: philip@igcar.gov.in; Raj, Baldev [Metallurgy and Materials Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India)

    2007-05-15

    We report the effect of initial pH and temperature of iron salt solutions on formation of magnetite (Fe{sub 3}O{sub 4}) nanoparticles during co-precipitation. We synthesized nanoparticles by keeping the initial pH at 0.7, 1.5, 3.0, 4.7, 5.7, 6.7 for two different temperatures of 30 and 60 deg. C. When the initial pH (prior to alkali addition) of the salt solution was below 5, the nanoparticles formed were 100% spinel iron oxide. Average size of the magnetite particles increases with initial pH until ferrihydrite is formed at a pH of 3 and the size remains the same till 4.7 pH. The percentage of goethite formed along with non-stoichiometric magnetite was 35 and 78%, respectively, when the initial pH of the solution was 5.7 and 6.7. As the reaction temperature was increased to 60 deg. C, maintaining a pH of 6.7, the amount of goethite increased from 78 to 100%. These results show that the initial pH and temperature of the ferrous and ferric salt solution before initiation of the precipitation reaction are critical parameters controlling the composition and size of nanoparticles formed. We characterize the samples using X-ray diffraction, transmission electron microscopy and vibrating sample magnetometer. The results of the present work provide the right conditions to synthesis pure magnetite nanoparticles, without goethite impurities, through co-precipitation technique for ferrofluid applications.

  10. Structural analysis of salt cavities formed by solution mining: I. Method of analysis and preliminary results for spherical cavities

    International Nuclear Information System (INIS)

    The primary objective of this effort is an analysis of the structural stability of cavities formed by solution mining in salt domes. In particular, the effects of depth (i.e. initial state of in situ stress), shape, volume (i.e. physical dimensions of the cavity), and sequence of salt excavation/fluid evacuation on the timewise structural stability of a cavity are of interest. It is anticipated that an assessment can be made of the interrelation between depth, cavern size, and cavern shape or of the practical limits therewith. In general, the cavity shape is assumed to be axisymmetric and the salt is assumed to exhibit nonlinear creep behavior. The primary emphasis is placed on the methodology of the finite element analysis, and the results of preliminary calculations for a spherically shaped cavity. It is common practice for engineers to apply elasticity theory to the behavior of rock in order to obtain near field stresses and displacements around an underground excavation in an effort to assess structural stability. Rock masses, particularly at depth, may be subjected to a rather complex state of initial stress, and may be nonhomogeneous and anisotropic. If one also includes complex geometrical excavation shape, the use of analytical techniques as an analysis tool is practically impossible. Thus, it is almost a necessity that approximate solution techniques be employed. In this regard, the finite element method is ideal as it can handle complex geometries and nonlinear material behavior with relative ease. An unusual feature of the present study is the incorporation into the finite element code of a procedure for handling the gradual creation or excavation of an underground cavity. During the excavation sequence, the salt is permitted to exhibit nonlinear stress-strain-time dependence. The bulk of this report will be devoted to a description of the analysis procedures, together with a preliminary calculation for a spherically shaped cavity

  11. Kinetic study of CO2 with various amino acid salts in aqueous solution

    NARCIS (Netherlands)

    Holst, van J.; Versteeg, G.F.; Brilman, D.W.F.; Hogendoorn, J.A.

    2009-01-01

    A study towards the kinetics of CO2 with several aqueous salts of amino acids was performed at a temperature of 298 K. Absorption rate experiments were carried out in the pseudo-first-order regime, enabling the determination of the kinetic rate constant from the flux. In a preliminary screening at a

  12. Kinetic study of CO2 with various amino acid salts in aqueous solution

    NARCIS (Netherlands)

    van Hoist, J.; Versteeg, G. F.; Brilman, D. W. F.; Hogendoorn, J. A.; Holst, J. v

    2009-01-01

    A study towards the kinetics Of CO2 with several aqueous salts of amino acids was performed at a temperature of 298 K. Absorption rate experiments were carried out in the pseudo-first-order regime, enabling the determination of the kinetic rate constant from the flux. In a preliminary screening at a

  13. Preparation of glass carbon electrode modified with nanocrystalline nickel-decorated carbon nanotubes and electrocatalytic oxidation of methanol in alkaline solution

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Nanocrystalline nickel with an average diameter of about 16 nm and a face-centered cubic (fcc)structure was uniformly attached to the surface of carbon nanotubes (CNT) by wet chemistry.The sample was characterized by X-ray powder diffraction and transmission electron microscopy (TEM).A glass carbon electrode modified with nickel-modified multi-wall carbon nanotubes (MWCNTs-Ni/GCE) was prepared.The electrochemical behavior of the MWCNTs-Ni/GCE and the electrocatalytic oxidation of methanol at the MWCNTsNi/GCE were investigated by cyclic voltammetry in 1.0 mol/L NaOH solution.The cyclic voltammograms showed that the electron transfer between β-Ni(OH)2 and β-NiOOH is mainly a diffusion-controlled quasireversible process,and that the electrode has high catalytic activity for the electrooxidation of methanol in alkaline medium,revealing its potential application in alkaline rechargeable batteries and fuel cells.

  14. Electrodeposition and characterization of Ni-MoO2 composite coatings as cathodes for the hydrogen evolution reaction in alkaline solution

    Directory of Open Access Journals (Sweden)

    Lačnjevac Uroš Č.

    2013-01-01

    Full Text Available Composite Ni-MoO2 coatings were prepared and characterized with respect to their possible application as electrocatalysts for the hydrogen evolution reaction (HER in alkaline solution. The composites were electrodeposited onto Ni meshes from an ammonium chloride Ni solution with suspended MoO2 particles in simulated industrial conditions for production of commercial cathodes. The influence of the concentration of MoO2 particles in the solution and deposition current density on the morphology, chemical and phase composition of obtained coatings was investigated by scanning electron microscopy (SEM, energy dispersive X-ray spectroscopy (EDS and X-ray diffraction (XRD. Catalytic activity for the HER of the coatings was examined by polarization measurements in a 32 wt. % NaOH solution at 90°C and compared to the activity of the commercial De Nora’s cathode (DN. It was shown that the most active Ni-MoO2 coating exhibits better polarization characteristics for the HER than the DN cathode. The mechanism of the HER on the specified Ni-MoO2 coating was investigated in 8 mol dm-3 NaOH at 30°C by means of steady-state polarization measurements and an electrochemical impedance spectroscopy (EIS method. Based on the theoretical interpretation of the experimental data, rate constants of the three individual steps of the HER were determined and the source of catalytic activity of the coating was elucidated. [Projekat Ministarstva nauke Republike Srbije, br. 172054

  15. Preparation of porous monolayer film by immersing the stearic acid Langmuir-Blodgett monolayer on mica in salt solution

    Science.gov (United States)

    Wang, S.; Li, Y. L.; Zhao, H. L.; Liang, H.; Liu, B.; Pan, S.

    2012-11-01

    Porous materials have drawn attention from scientists in many fields such as life sciences, catalysis and photonics since they can be used to induce some materials growth as expected. Especially, porous Langmuir-Blodgett (LB) film is an ideal material with controlled thickness and flat surface. In this paper, stearic acid (SA), which has been extensively explored in LB film technique, is chosen as the template material with known parameters to prepare the LB film, and then the porous SA monolayer film is obtained by means of etching in salt solution. The main etching mechanism is suggested that the cations in the solution block the electrostatic interaction between the polar carboxyl group of SA and the electronegative mica surface. The influencing factors (such as concentration of salt solution, valence of cation and surface pressure) of the porous SA film are systematically studied in this work. The novel method proposed in this paper makes it convenient to prepare porous monolayer film for designed material growth or cell culture.

  16. Effect of ammonium-salt solutions on the surface properties of carbon fibers in electrochemical anodic oxidation

    International Nuclear Information System (INIS)

    Highlights: ► Longitudinal grooves on the fiber surface became more well-defined and much deeper after surface treatment. ► The concentration of oxygen and nitrogen on the fiber surface increased after surface treatment. ► The intensity of oxidative reaction varied with the change of ammonium-salt solutions. ► The higher the concentration of OH− ions in the electrolytes, the violent the oxidative reaction happened. - Abstract: The surfaces of polyacrylonitrile-based carbon fibers were treated by an electrochemical anodic method. Three different kinds of ammonium-salt solutions namely NH4HCO3, (NH4)2CO3 and (NH4)3PO4 were respectively chosen as the electrolytes. The effect of these electrolytes on the surface structure was studied by scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). The results showed that longitudinal grooves on the fiber surface became more well-defined and much deeper after surface treatment, and the root mean square roughness (RMS) of carbon fiber surface increased from 4.6 nm for untreated fibers to 13.5 nm for treated fibers in (NH4)3PO4 electrolytes. The concentration of oxygen and nitrogen atomic on the fiber surface increased after surface treatment. The tensile strength of oxidized fibers had an obvious decrease, whereas the interlaminar shear strength (ILSS) value of corresponding carbon fiber reinforced polymers (CFRPs) increased in a large extent. The intensity of oxidative reaction varied with the change of ammonium-salt solutions and electrochemical oxidation in (NH4)3PO4 electrolyte was of the most violence. The corresponding mechanism was also discussed and the result showed that the higher the concentration of OH− ions in the electrolytes, the violent the oxidative reaction happened.

  17. Anodization of AZ91 magnesium alloy in alkaline solution containing silicate and corrosion properties of anodized films

    Institute of Scientific and Technical Information of China (English)

    LI Ling-ling; CHENG Ying-liang; WANG Hui-min; ZHANG Zhao

    2008-01-01

    The anodization of AZ91 magnesium alloy in an alkaline electrolyte of 100g/L NaOH+20g/L Na2B4O7·10H2O+50g/L C6H5Na3O7·2H2O+60g/L Na2SiO3·9H2O was studied.The corrosion resistance of the anodized films was studied by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques.The microstructure of the films was examined with scanning electronic microscope (SEM) and X-ray diffractometer (XRD).The results show that,under the experimental conditions,the optimum anodizing time and the optimum anodizing current density are 40min and 20mA/cm2 respectively for obtaining the anodic film with high corrosion resistance.The XRD pattern shows that the components of the anodized film consist of MgO and Mg2 (SiO4).

  18. Evaluation of packed-bed and fluidized-bed cell technology for the destruction and removal of contaminants in alkaline waste solutions. Final report

    International Nuclear Information System (INIS)

    Disposing of the large quantity of nuclear waste that has been produced within the DOE complex is an area of active research and development. Electrochemical processes have been reported for the treatment of alkaline wastes including the destruction of nitrate and nitrite and the removal of metals such as Tc and Ru. Electrolytic recovery of metals from dilute solution has been reported using conventional porous electrodes such as felt electrode and reticulated electrode, but use of such electrodes is limited. The pores of such electrodes become blocked as a consequence of metal deposition. If an attempt is made to regenerate these electrodes by dissolution of the deposited metals, oxygen evolution on the matrix competes with dissolution of metals deposited within the pores. On the other hand, the use of three dimensional packed-bed and fluidized-bed electrodes having large surface area per unit volume would offer an improvement on felt or reticulated system because of the greater ease of regeneration

  19. Evaluation of packed-bed and fluidized-bed cell technology for the destruction and removal of contaminants in alkaline waste solutions. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D.T. [Westinghouse Savannah River Co., Aiken, SC (United States); Bockris, J.O.M.; Kim, Jinseong [Texas A& M Univ., College Station, TX (United States). Surface Electrochemistry Laboratory

    1995-12-31

    Disposing of the large quantity of nuclear waste that has been produced within the DOE complex is an area of active research and development. Electrochemical processes have been reported for the treatment of alkaline wastes including the destruction of nitrate and nitrite and the removal of metals such as Tc and Ru. Electrolytic recovery of metals from dilute solution has been reported using conventional porous electrodes such as felt electrode and reticulated electrode, but use of such electrodes is limited. The pores of such electrodes become blocked as a consequence of metal deposition. If an attempt is made to regenerate these electrodes by dissolution of the deposited metals, oxygen evolution on the matrix competes with dissolution of metals deposited within the pores. On the other hand, the use of three dimensional packed-bed and fluidized-bed electrodes having large surface area per unit volume would offer an improvement on felt or reticulated system because of the greater ease of regeneration.

  20. Removal of fission and corrosion products from alkaline solutions of boric acid by the ion exchange method

    International Nuclear Information System (INIS)

    Results are given for ion exchange on organic resines method application in experiments on removal of some fission products and corrosion products from solutions containing boric acid. As it is known, presence of boric acid in solution makes it difficult radioactive wastes processing, concentration and solidification. The main task of the investigation was to develop methods for boric acid regeneration from the coolant of primary coolant circuits of nuclear power plant. Special attention was pade to investigations on cesium sorption from the boric acid solutions, containing potassium ions. It was shown that by means of acidulation of solutions, increase of efficiency of radioactive wastescontaining boric acin by mens of ion exchange is gained. But this method is practical only in the case when solution is not returned into the primary coolant circuit after purification. Expediency of preliminary removal of cesium from solution by means of selective nonorganic ionites is shown. Attention is called to the danger of boric acid for natural waters and danger of liquid wastes containing boric acid even after removal of radionuclides from them. (I.T.)

  1. The effect of high pH alkaline solutions on the mineral stability of the Boom Clay - Batch experiments at 60 deg. C

    International Nuclear Information System (INIS)

    Boom Clay is currently viewed as a reference host formation for studies on deep geological disposal of radioactive waste in Belgium. The interactions between bulk rock Boom Clay and 0.1 M KOH, 0.1 M NaOH, 0.1 M Ca(OH)2, young cement water and evolved cement water solutions, ranging in pH from 12.5 to 13.2, were examined as static batch experiments at 60 deg. C to simulate alkaline plume perturbations, which are expected to occur in the repository due to the presence of concrete. Both liquids and solids were investigated at specific times between 90 and 510 days in order to control the elemental budget and to search for potential mineralogical alterations. Also, the clay fraction was separated from the whole-rock Boom Clay at the end of each run and characterized for its mineralogical composition. Thereby, the importance of the mineral matrix to buffer the alkaline attack and the role of organic matter to protect clay minerals were also addressed. The results indicate that the degree of geochemical perturbation in Boom Clay is dependent on the initial pH of the applied solution together with the nature of the major cation in the reactant fluids. The higher the initial pH of the media, the stronger its interaction with Boom Clay. No major non-clay mineralogical alteration of the Boom Clay was detected, but dissolution of kaolinite, smectite and illite occurred within the studied experimental conditions. The dissolution of clays is accompanied by the decrease in the layer charge, followed by a decrease in the cation-exchange capacity. The highest TOC values coincide with the highest total elemental concentrations in the leachates, and correspondingly, the highest dissolution degree. However, no quantitative link could be established between the degree of organic matter decomposition and clay dissolution.

  2. Spiropyran salts and their neutral precursors: synthesis, crystal structure, photochromic transformations in solutions and solid state

    Science.gov (United States)

    Yurieva, E. A.; Aldoshin, S. M.

    2015-06-01

    This review covers investigations of spiropyran iodides with N-substituted indoline fragment, and with the pyran cycle being annelated to N-methylated pyridine ring. The schemes of synthesis of iodides and their neutral precursors, as well as results of X-ray analysis and photochemical study of the crystals of the obtained compounds are presented. Based on our and literature data, the relationship between the structure and photochromic properties has been discussed for a series of salts and neutral pyridospiropyrans.

  3. Activity coefficients of ferrocenium iodide in aqueous-organic salt solutions

    International Nuclear Information System (INIS)

    Values of electrode potentials were obtained by the method of potentiometric titration at 298.2 K, the standard values of emf and unified activity coefficients of ferrocenium iodide in water-acetone and water-ethanol solvents of different salt composition being calculated. It is shown that interaction of ferrocenium (Fc+) with iodide can occur with formation of two forms of complexes, i.e. [Fc+I-] and [Fc+I2]-

  4. Viscosity Behavior of α-Amino Acids in Acetate Salt Solutions at Temperatures (303.15 to 323.15) K

    Science.gov (United States)

    Siddique, Jamal Akhter; Naqvi, Saeeda

    2012-01-01

    Viscosities of l-lysine monohydrochloride, l-histidine, and l-arginine in 1 m (mol · kg-1) aqueous solutions of sodium acetate, potassium acetate, and calcium acetate salts has been determined at (303.15, 308.15, 313.15, 318.15, and 323.15) K. The Falkenhagen coefficient, A, and Jones-Dole coefficient, B, relative viscosity, and specific viscosity of the solutions have also been determined using the measured viscosities. The results are interpreted in terms of solute-solute and solute-solvent interactions occurring in the system under investigation and also discussed in terms of the structure-making/breaking ability of the solute in these salt solutions. The structure making/breaking abilities of the solutes in the studied systems are strongly influenced by temperature.

  5. An optimization study on removal of Zn from aqueous solution by ultrasound assisted preparation of activated carbon from alkaline impregnated hazelnut shell

    International Nuclear Information System (INIS)

    Nowadays, ultrasound has gained importance in a wide variety of industrial fields especially in wastewater and sewage treatment. Ultrasound exhibits several beneficial effects in solid liquid systems by means of the cavitations phenomenon by causing the formation of many microcracks on the solid surface; thus, it increases the surface area between the reactants and cleans solid reactant or catalyst particle surfaces. In this study, activated carbon adsorbent for removing heavy metal cations such as Zn2+ from aqueous solutions has been prepared. For this purpose, KOH solution was impregnated into hazelnut shells under ultrasonic irradiation. After filtration, hazelnut shells have been carbonized under inert N2 atmosphere. The experiments were planned by statistical design methods. Finally, activated carbons were characterized by the evolution of their zinc adsorption capacity. Optimum preparation conditions were obtained by using constrained optimization program by means of the Matlab computer software. Activated carbon with the maximum adsorption capacity was further characterized by using scanning electron microscopy. The alkaline impregnation into hazelnut shells under ultrasonic irradiation was found to be beneficial for preparation of activated carbon for use as adsorbents to remove Zn2+ from aqueous solutions. (author)

  6. Enhanced removal of trace Cr(VI) from neutral and alkaline aqueous solution by FeCo bimetallic nanoparticles.

    Science.gov (United States)

    Qin, Nannan; Zhang, Ya; Zhou, Hongjian; Geng, Zhigang; Liu, Gang; Zhang, Yunxia; Zhao, Huijun; Wang, Guozhong

    2016-06-15

    The reactivity of zero valent iron (Fe(0)) for removing Cr(VI) is self-inhibiting under neutral and alkaline conditions, due to the precipitation of ferrous hydroxide on the surface of Fe(0). To overcome this difficulty, we incorporated a second metal (Co) into Fe(0) to form FeCo bimetallic nanoparticles (FeCo BNPs), which can achieve higher activity and significant improvement in the reaction kinetics for the removal of Cr(VI) compared with Fe(0). The FeCo BNPs were synthesized by a hydrothermal reduction method without using any templates. The characterization analysis indicated that the products were highly uniform in large scale with 120-140nm size in diameter. The obtained FeCo BNPs exhibited a remarkable removal ability for Cr(VI) in the pH range of 5.3-10.0. Especially, FeCo BNPs were able to reduce trace Cr(VI) (1.0mgL(-1), pH=7.5) down to about 0.025mgL(-1) within 1h. XPS analysis confirmed that Cr(VI) was reduced to Cr(III) by FeCo BNPs, while Fe and Co was oxidized, implying a chemical reduction process. The enhanced removal of trace Cr(VI) could be originated from the introduction of Co, which not only served as a protecting agent against surface corrosion by galvanic cell effect, but also enhanced the efficient flow of electron transfer between iron and Cr(VI). All the results primarily imply that FeCo BNPs can be employed as high efficient material for wastewater treatment. PMID:26998785

  7. Dielectric relaxation and underlying dynamics of electrolyte solutions and solvent-molten salt mixtures using terahertz time-domain transmission spectroscopy

    Science.gov (United States)

    Asaki, Melanie Lynette Thongs

    Terahertz (THz) transmission spectroscopy is used to obtain the frequency dependent complex dielectric constants of water, methanol, and propylene carbonate, and solutions of lithium salts in these solvents, as well as mixtures of acetonitrile and a room-temperature molten salt. The behavior of the pure solvents is modeled with either two (water and acetonitrile) or three (methanol and propylene carbonate) Debye relaxations. For solutions of lithium salts, the effects of ionic solvation on the relaxation behavior of the solvents is discussed in terms of modifications to the values of the Debye parameters of the pure solvents. In this way we obtain estimates for numbers of irrotationally bound solvent molecules, the numbers of bonds broken or formed, and the effects of ions on the higher frequency relaxations. The same information was obtained for molten salt-acetonitrile systems. In addition, it was determined that at low molten salt concentrations, the mixtures behave like electrolyte solutions of a crystalline salt dissolved in a solvent. At higher molten salt concentrations, the behavior is that of a mixture of two liquids.

  8. Separation of actinides with alkylpyridinium salts

    International Nuclear Information System (INIS)

    Various f-elements are separated as anionic complexes from both acidic and alkaline solutions by precipitation with alkylpyridinium salts. The precipitates are also cationic surfactants where the simple counter-ion (e.g. nitrate or chloride) is replaced by the negatively charged complex anion of an actinide or lanthanide. The low solubility of these precipitates is explained by a strong affinity of divalent complex counter-ions of f-elements to the quaternary nitrogen. Precipitations in solutions of nitric acid allow to separate tetravalent f-elements from other metals, in alkaline carbonate solutions tetravalent and hexavalent actinides are precipitated simultaneously. The last procedure yields precipitates, which are very intimate mixtures of hexavalent and tetravalent actinides. This allows to prepare mixed oxides in a simple way. (author) 6 refs.; 3 figs.; 3 tabs

  9. Limitations of amorphous content quantification by isothermal calorimetry using saturated salt solutions to control relative humidity: alternative methods.

    Science.gov (United States)

    Khalef, Nawel; Pinal, Rodolfo; Bakri, Aziz

    2010-04-01

    Despite the high sensitivity of isothermal calorimetry (IC), reported measurements of amorphous content by this technique show significant variability even for the same compound. An investigation into the reasons behind such variability is presented using amorphous lactose and salbutamol sulfate as model compounds. An analysis was carried out on the heat evolved as a result of the exchange of water vapor between the solid sample during crystallization and the saline solution reservoir. The use of saturated salt solutions as means of control of the vapor pressure of water within sealed ampoules bears inherent limitations that lead in turn to the variability associated with the IC technique. We present an alternative IC method, based on an open cell configuration that effectively addresses the limitations encountered with the sealed ampoule system. The proposed approach yields an integral whose value is proportional to the amorphous content in the sample, thus enabling reliable and consistent quantifications. PMID:19774655

  10. Inclusion of two push-pull N-methylpyridinium salts in anionic surfactant solutions: a comprehensive photophysical investigation.

    Science.gov (United States)

    Cesaretti, Alessio; Carlotti, Benedetta; Consiglio, Giuseppe; Del Giacco, Tiziana; Spalletti, Anna; Elisei, Fausto

    2015-06-01

    Two N-methylpyridinium salts with push-pull properties have been investigated in the aqueous solution of anionic micelles of sodium dodecyl sulfate (SDS) and potassium p-(octyloxy)benzenesulfonate (pOoBSK) surfactants. These molecules are known to be extremely sensitive to the local environment, with their absorption spectrum being subjected to a net negative solvatochromism. These compounds are also characterized by an excited state deactivation strictly dependent on the physical properties of the chemical surrounding, with the formation of intramolecular charge-transfer (ICT) states accordingly stabilized. Thanks to steady-state and femtosecond resolved spectroscopic techniques, the photophysical properties of these molecules in the presence of anionic micelles have been fully characterized and an efficient permeation within the micellar aggregates can thus be inferred. The extent of the changes in the photophysical properties of these molecules (with respect to what is observed in water) is an indicator of the medium experienced in the nanoheterogeneous solutions: enhanced fluorescence emissions, reduced Stokes shifts and slowed-down excited state decays strongly confirm the confinement within a scarcely polar and restraining environment. The slightly different behavior shown in the two types of micelles can be ascribed to a peculiar interaction between the aromatic moiety of the surfactant and that of the cations. Additionally, the inclusion promotes the solubilization of these poorly water-soluble salts, which is alluring in their promising use as DNA binders for antitumor purposes. Thus, the anionic micelles allowed the solubilization of the pyridinium salts under investigation, which in turn allowed the characterization of the nonhomogeneous medium established by the micellar aggregates. PMID:25945687

  11. The corrosion and electrochemical behavior of pure aluminum in additive-containing alkaline methanol-water mixed solutions

    Energy Technology Data Exchange (ETDEWEB)

    Wang, J.B.; Wang, J.M.; Shao, H.B.; Chang, X.T.; Wang, L. [Department of Chemistry, Zhejiang University, Hangzhou (China); Zhang, J.Q.; Cao, C.N. [Department of Chemistry, Zhejiang University, Hangzhou (China); State Key Laboratory for Corrosion and Protection of Metal, Institute of Metal Research, Chinese Academy of Sciences, Shenyang (China)

    2009-04-15

    The corrosion and electrochemical behavior of aluminum in inhibited and uninhibited 4 M KOH-methanol-water mixed solutions with a methanol/water volume ratio of 3:2 were investigated by means of hydrogen collection, polarization curve, galvanostatic discharge, and electrochemical impedance spectroscopy (EIS). The results of hydrogen collection and electrochemical experiments showed that the addition of ZnO can obviously inhibit the corrosion of aluminum in the 4 M KOH-methanol-water solutions, and its inhibition effect can be enhanced in the hydroxytryptamine (HT)-containing KOH solution. The results of scanning electron microscopy (SEM) and energy dispersive analysis of X-ray (EDAX) revealed that ZnO produces the inhibition effect by the formation of a zinc-containing deposit layer on the surface of aluminum, and the cooperative effect of ZnO and HT may improve the deposit of zinc. The results of galvanostatic discharge indicated that aluminum can present good electrochemical activity in the 4 M KOH-methanol-water solution with 0.2 M ZnO and 1.0 mL/L HT. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  12. Effect of salt and phosphorus concentrations, pH and temperature of the nutrient solution on wheat primary root growth

    International Nuclear Information System (INIS)

    Extensive primary root growth is very important for field set up in wheat (Triticum aestivum L.) production in upland conditions in the State of Sao Paulo, Brazil. Fourteen wheat genotypes (mutant lines and cultivars) were each evaluated for their primary root growth at 7 and 15 days after germination in aerated nutrient solutions. The effects of salt concentrations, temperature, pH and phosphorus concentration on primary root growth were studied. High genetic variability of primary root growth was observed. The genotype BH-1146 presented the best genetic potential for root growth at all solution salt concentrations and temperatures, while genotypes BH-1146, KAUZ''S''/IAC-24 M2, KAUZ''S''/IAC-24 M8, IAC-24/TUI''S'' M2, TUI''S''/IAC-24 M1 and TUI''S'', showed better potential over the others at all P concentrations and pHs. Separate heritability studies were also conducted and they revealed that primary root growth was influenced by a few genes exhibiting partial dominant behavior. (author)

  13. Ice VII from aqueous salt solutions: From a glass to a crystal with broken H-bonds.

    Science.gov (United States)

    Klotz, S; Komatsu, K; Pietrucci, F; Kagi, H; Ludl, A-A; Machida, S; Hattori, T; Sano-Furukawa, A; Bove, L E

    2016-01-01

    It has been known for decades that certain aqueous salt solutions of LiCl and LiBr readily form glasses when cooled to below ≈160 K. This fact has recently been exploited to produce a « salty » high-pressure ice form: When the glass is compressed at low temperatures to pressures higher than 4 GPa and subsequently warmed, it crystallizes into ice VII with the ionic species trapped inside the ice lattice. Here we report the extreme limit of salt incorporation into ice VII, using high pressure neutron diffraction and molecular dynamics simulations. We show that high-pressure crystallisation of aqueous solutions of LiCl∙RH2O and LiBr∙RH2O with R = 5.6 leads to solids with strongly expanded volume, a destruction of the hydrogen-bond network with an isotropic distribution of water-dipole moments, as well as a crystal-to-amorphous transition on decompression. This highly unusual behaviour constitutes an interesting pathway from a glass to a crystal where translational periodicity is restored but the rotational degrees of freedom remaining completely random. PMID:27562476

  14. Aggregation and antigenicity of virus like particle in salt solution--A case study with hepatitis B surface antigen.

    Science.gov (United States)

    Chen, Yi; Zhang, Yan; Quan, Can; Luo, Jian; Yang, Yanli; Yu, Mengran; Kong, Yingjun; Ma, Guanghui; Su, Zhiguo

    2015-08-20

    The phenomenon of aggregation of virus-like particles (VLPs) in salt solution and the corresponding effect upon antigenicity was reported. Asymmetrical flow field-flow fractionation (AF4) combined with multi-angle laser light scattering (MALLS) was used to characterize the size and the aggregation behavior of hepatitis B surface antigen (HBsAg). The average diameter of HBsAg VLP was 22.8±0.4 nm and it tended to aggregate in salt solution to form large particles and the antigenicity changed accordingly. In 0-4 M NaCl solution, part of HBsAg molecules aggregated rapidly into oligomeric particles (OP), whose diameter distributed from 25 to 40 nm, and the antigenicity slightly decreased about 10%. The aggregation reaction is reversible. After removing NaCl, both size and antigenicity could recover to normal level (92-96%). By contrast, the aggregation process is more complicated in (NH4)2SO4 solution. Most of HBsAg particles aggregated into OP and further aggregated into polymeric particles (PP). The diameter of the PP could reach 40 to 140 nm. The concentration of (NH4)2SO4 had remarkable influence upon the rate of aggregation. When concentration of (NH4)2SO4 was below 1 M, most of HBsAg aggregated only into OP in 1 h. While with concentration of (NH4)2SO4 above 1 M, most of particles formed PP within 1 h. The aggregation process to PP was irreversible. After removing (NH4)2SO4, the large aggregates could not recover to normal particles and the remaining antigenicity was below 30%. PMID:25862298

  15. Non-trivial solution chemistry between amido-pyridylcalix[4]arenes and some metal salts

    OpenAIRE

    Colleran, John; Creaven, Bernadette; Donlon, Denise; MCGINLEY John

    2010-01-01

    Mercury ion complexation reactions were carried out between 3 and various mercury(II) salts. 1H NMR studies showed that the role of solvent, the anion chosen and the initial reaction conditions were critical and that the formation of a “simple” mercury(II) complex was non-trivial. The mercury(II) ion can cause either (i) the formation of an ion-pair system, which have a characteristic doubling of all signals in the 1H NMR spectrum, (ii) a cleavage reaction to occur resulting in the reformatio...

  16. Electrochemical and surface studies on the passivity of a dental Pd-based casting alloy in alkaline sulphide solution

    International Nuclear Information System (INIS)

    The corrosion and tarnish behavior of a dental casting Pd-25Ag-18Cu-12Au alloy in 0.1% Na2S solution at 37 deg. C was investigated using potentiodynamic polarization and spectrocolorimetric techniques. The surface film was characterized by X-ray photoelectron spectroscopy (XPS). This alloy exhibited markedly higher resistance to corrosion and tarnish than did the Ag-20Pd-18Cu-12Au alloy in current clinical use. XPS spectra indicated the presence of a thin sulphide film composed of PdS. It was found that the PdS film is very protective and is responsible for the passivity of the Pd-25Ag-18Cu-12Au alloy in 0.1% Na2S solution

  17. Room temperature phosphorescence lifetime and quantum yield of erythrosine B and rose bengal in aerobic alkaline aqueous solution

    International Nuclear Information System (INIS)

    The room-temperature phosphorescence behavior of erythrosine B (ER) and rose bengal (RB) in aerobic aqueous solution at pH 10 (10−4 M NaOH) is investigated. The samples were excited with sliced second harmonic pulses of a Q-switched Nd:glass laser. A gated photomultiplier tube was used for instantaneous fluorescence signal discrimination and a digital oscilloscope was used for signal recording. For phosphorescence lifetime measurement the oscilloscope response time was adjusted to appropriate time resolution and sensitivity by the ohmic input resistance. In the case of phosphorescence quantum yield determination the gated photomultiplier – oscilloscope arrangement was operated in integration mode using 10 MΩ input resistance. Phosphorescence quantum yield calibration was achieved with erythrosine B and rose bengal doped starch films of known quantum yields. The determined phosphorescence lifetimes (quantum yields) of ER and RB in 0.1 mM NaOH are τP=1.92±0.1 μs (φP=(1.5±0.3)×10−5) and 2.40±0.1 μs ((5.7±0.9)×10−5), respectively. The results are discussed in terms of triplet state deactivation by dissolved molecular oxygen. - Highlights: ► Phosphorescence lifetime of fluorone dyes in aerobe aqueous solution is measured. ► Phosphorescence quantum yield of fluorone dyes in aerobe solution is determined. ► Experimental setup with Q-switched laser and gated PMT detection is described. ► Phosphorescence quenching by dissolved molecular oxygen is analyzed. ► Absorption and fluorescence behavior of fluorones in aqueous solution is studied.

  18. Computer modeling of the local structure, mixing properties, and stability of solid solutions of alkaline-earth metal oxides

    International Nuclear Information System (INIS)

    A technique for the computer modeling of disordered binary oxide solid solutions MO-M'O in a wide composition range has been developed. The method of atomistic pair potentials was used for 4 x 4 x 4 supercells. The parameters of the potentials are optimized using the structural and elastic properties of pure components MgO, CaO, SrO, and BaO. The temperature dependences of the heat capacity and entropy are calculated for pure components. The excess mixing properties (enthalpy, volume, bulk modulus, vibrational entropy) are found for different compositions of MgxCa(1-x)O, CaxSr(1-x)O, and SrxBa(1-x)O solid solutions. Temperature and composition dependences of the excess Gibbs energy were constructed, which made it possible to approximately estimate the critical decomposition temperatures and limits of component miscibility. Statistical analysis of lattice distortions in the first and second coordination spheres reveals a detailed picture of the solid-solution local structure.

  19. Novel one-step synthesis of wool-ball-like Ni-carbon nanotubes composite cathodes with favorable electrocatalytic activity for hydrogen evolution reaction in alkaline solution

    Science.gov (United States)

    Chen, Zhouhao; Ma, Zhipeng; Song, Jianjun; Wang, Lixin; Shao, Guangjie

    2016-08-01

    In this work, supergravity fields are performed to prepare Ni-CNTs composite cathodes with wool-ball-like morphology from the Watts bath containing well-distributed functionalized CNTs. The prepared Ni-CNTs composite cathodes are used as noble metal-free electrocatalyst with favorable electrocatalytic activity for hydrogen evolution reaction (HER) in alkaline solutions. The crystal structure and morphology of the composite cathodes are characterized by XRD and SEM measurements. The electrochemical activities of the cathodes are characterized through Tafel polarization measurement, electrochemical impedance spectroscopy and cyclic voltammetric study in 1.0 M NaOH solution. The results indicate that catalytic activities of the Ni-CNTs cathodes prepared under supergravity fields are enhanced significantly, and the sample prepared at rotating speed 3000 rpm from the bath containing 1 g dm-3 CNTs exhibits the highest HER activity with smallest Tafel slope and largest exchange current density of 823.9 μA cm-2. Furthermore, the effects of both the CNTs concentrations and the intensities of supergravity fields on the properties of the Ni-CNTs cathodes are investigated.

  20. 用酚酞检测碱性电池密封性的探讨%Study on phenolphthalein solution to detect the sealing characteristics of alkaline cell

    Institute of Scientific and Technical Information of China (English)

    宋清山

    2001-01-01

    The causes of producing error results were analyzed at detectingalkaline cell seal characteristics,using phenolphthalein solution. The results of experiment indicated that condition of environment humidity were higher,water was electrolysed on the sealing position,the possible of producing error results could increase.In order to increase reliability using phenolphthalein solution to detect alkaline cell sealing characteristics,the water in the alcohol was decreased, environment humidity were requisite.%分析了用酚酞试剂检测碱性电池密封性能产生错误结果的原因。实验结果表明:在环境湿度较高的条件下,碱性电池密封处的水膜就会被电解,产生错误的可能性就会大大增加。为了提高酚酞溶液检测碱性电池密封性能的可靠性,就必须减少配制酚酞试剂酒精中的含水量,同时也必须降低测试环境湿度。

  1. Non-monotonic course of protein solubility in aqueous polymer-salt solutions can be modeled using the sol-mxDLVO model.

    Science.gov (United States)

    Herhut, Marcel; Brandenbusch, Christoph; Sadowski, Gabriele

    2016-02-01

    Protein purification is often performed using cost-intensive chromatographic steps. To discover economic alternatives (e.g., crystallization), knowledge on protein solubility as a function of temperature, pH, and additives in solution as well as their concentration is required. State-of-the-art models for predicting protein solubility almost exclusively consider aqueous salt systems, whereas "salting-in" and "salting-out" effects induced by the presence of an additional polymer are not considered. Thus, we developed the sol-mxDLVO model. Using this newly developed model, protein solubility in the presence of one salt and one polymer, especially the non-monotonic course of protein solubility, could be predicted. Systems considered included salts (NaCl, Na-p-Ts, (NH(4))(2) SO(4)) and the polymer polyethylene glycol (MW: 2000 g/mol, 12000 g/mol) and proteins lysozyme from chicken egg white (pH 4 to 5.5) and D-xylose ketol-isomerase (pH 7) at 298.15 K. The results show that by using the sol-mxDLVO model, protein solubility in polymer-salt solutions can be modeled in good agreement with the experimental data for both proteins considered. The sol-mxDLVO model can describe the non-monotonic course of protein solubility as a function of polymer concentration and salt concentration, previously not covered by state-of-the-art models. PMID:26579880

  2. Recovery of uranium from loaded resin of processing in-situ leaching solution by alkaline elution system

    International Nuclear Information System (INIS)

    Sodium carbonate-ammonium sulfate solution is used as an eluant to elute uranium from loaded resin in the compact moving-bed column. Uranium concentration is up to about 10 g/L in eluate. The eluate is then heated to precipitate uranium and recover chemicals. The prepared yellow cake contains 60% of moisture and >60% of uranium (based on dried yellow cake). About 70% of CO2 and nearly all NH3 are recovered by condensing and absorbing from released gases during heating process of the eluate. The recovered chemicals and mother liquor after precipitation can be recycled for reuse

  3. Molten-salt synthesis and composition-dependent luminescent properties of barium tungsto-molybdate-based solid solution phosphors

    Science.gov (United States)

    Xiang-Hong, He; Zhao-Lian, Ye; Ming-Yun, Guan; Ning, Lian; Jian-Hua, Sun

    2016-02-01

    Pr3+-activated barium tungsto-molybdate solid solution phosphor Ba(Mo1-zWz)O4:Pr3+ is successfully fabricated via a facile molten-salt approach. The as-synthesized microcrystal is of truncated octahedron and exhibits deep-red-emitting upon blue light excitation. Powder x-ray diffraction and Raman spectroscopy techniques are utilized to investigate the formation of solid solution phosphor. The luminescence behaviors depend on the resulting composition of the microcrystals with fixed Pr3+-doping concentration, while the host lattices remain in a scheelite structure. The forming solid solution via the substitution of [WO4] for [MoO4] can significantly enhance its luminescence, which may be due to the fact that Ba(Mo1-zWz)O4:Pr3+ owns well-defined facets and uniform morphologies. Owing to its properties of high phase purity, well-defined facets, highly uniform morphologies, exceptional chemical and thermal stabilities, and stronger emission intensity, the resulting solid solution phosphor is expected to find potential applications in phosphor-converted white light-emitting diodes (LEDs). Project supported by the Construction Fund for Science and Technology Innovation Group from Jiangsu University of Technology, China, the Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, China (Grant No. KHK1409), the Priority Academic Program Development of Jiangsu Higher Education Institutions, China, and the National Natural Science Foundation of China (Grant No. 21373103).

  4. Chemical Corrosion of Liquid-Phase Sintered SiC in Acidic/Alkaline Solutions Part 1. Corrosion in HNO3 Solution

    Science.gov (United States)

    Zhang, Lei; Zhang, Ming; He, Xinnong; Tang, Wenming

    2016-03-01

    The corrosion behavior of the liquid-phase sintered SiC (LPS-SiC) was studied by dipping in 3.53 mol/L HNO3 aqueous solution at room temperature and 70 °C, respectively. The weight loss, strength reduction and morphology evolution of the SiC specimens during corroding were revealed and also the chemical corrosion process and mechanism of the SiC specimens in the acidic solution were clarified. The results show that the corrosion of the LPS-SiC specimens in the HNO3 solution is selective. The SiC particles are almost free from corrosion, but the secondary phases of BaAl2Si2O8 (BAS) and Y2Si2O7 are corroded via an acid-alkali neutralization reaction. BAS has a higher corrosion rate than Y2Si2O7, resulting in the formation of the bamboo-leaf-like corrosion pits. As the SiC specimens etched in the HNO3 solution at room temperature for 75 days, about 80 μm thickness corrosion layer forms. The weight loss and bending strength reduction of the etched SiC specimens are 2.6 mg/cm2 and 52%, respectively. The corrosion of the SiC specimens is accelerated in the 70 °C HNO3 solution with a rate about five times bigger than that in the same corrosion medium at room temperature.

  5. Conformation dynamics and polarization effect of α,α-trehalose in a vacuum and in aqueous and salt solutions.

    Science.gov (United States)

    Kan, Zigui; Yan, Xiufen; Ma, Jing

    2015-03-01

    Conformational changes of α,α-trehalose in a vacuum, water, and 0-20 wt % NaCl solutions were investigated by means of molecular dynamics (MD) simulations at different levels of density function theory (DFT) and with fixed-charge nonpolarizable and variable-charge force fields (FFs), respectively. The relative thermodynamic stability of trehalose is enhanced by the formation of intercycle and/or intracycle hydrogen bonds, but some thermodynamically unfavorable structures can be sampled in the DFT-based ab initio MD simulation. The polarization effects of polar trehalose molecule in aqueous and NaCl solutions were studied by a series of MD simulations with both the conventional nonpolarizable and polarizable force field models. In the polarizable model, the partial charges of trehalose were updated every 2 ps using DFT calculations and fused with the other FF parameters for the energy calculation and MD simulation. Around the trehalose, water molecules located in an asymmetry model and trehalose have a stronger tendency to bind with water molecules than Na(+) and Cl(-) ions. When the trehalose concentration is increased from 3.26 to 6.31 wt % in salt aqueous solution, the two trehalose molecules periodically approach each other in a nearly anhydrate state and leave a way to keep the favorable hydration structure with the mean trehalose-trehalose distance of 8.6 Å. The similarity between the solvated dimer packing styles (shoulder-by-shoulder or head-to-head) and crystal stacking can be used to make an extrapolation to higher sugar concentrations and to rationalize the bioprotection function of trehalose in high salt concentration. PMID:25506668

  6. Frictional properties of the end-grafted polymer layer in presence of salt solution

    Science.gov (United States)

    Raftari, Maryam; Zhang, Zhenyu; Leggett, Graham J.; Geoghegan, Mark

    2012-02-01

    We have studied the frictional behaviour of grafted poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) films using friction force microscopy (FFM). The films were prepared on native oxide-terminated silicon substrates using the technique of atom transfer radical polymerization (ATRP). These brushes had constant grafting density (1.18 nm2), and of a thickness of ˜66 nm, as measured by ellipsometry. We show that single asperity contact mechanics (Johnson-Kendall-Roberts (JKR) and Derjaguin-M"uller-Toporov (DMT) models) as well as a linear (Amontons) relation between applied load and frictional load all apply to these systems depending on the concentration of salt and the nature of the FFM probe. Measurements were made using gold-coating and polymer functionalized silicon nitride triangular probes. Polymer functionalized probe included growth the PDMAEMA with same method on tips. The frictional behaviour are investigated between PDMAEMA and gold coated and PDMAEMA tips immersed in different concentrations of KCl, KBr and KI.

  7. From rice starch to amylose crystals : alkaline extraction of rice starch, solution properties of amylose and crystal structure of V-amylose inclusion complexes

    OpenAIRE

    Cardoso, Mateus

    2007-01-01

    The main purposes of the present work were to monitor the alkaline extraction of a Brazilian rice starch, to study the hydrodynamic behavior of amylose, a biopolymer extracted from starch, and to study the crystallization of V-amylose inclusion compounds. The efficiency of the alkaline deproteinization was evaluated using the Biuret test as well as UV-vis and fluorescence spectroscopy. In parallel, the morphological changes in starch granules and their alkaline gelatinization were studied. Th...

  8. Effect of ammonium-salt solutions on the surface properties of carbon fibers in electrochemical anodic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Qian Xin, E-mail: qx3023@nimte.ac.cn [National Engineering Laboratory of Carbon Fiber Preparation Technology, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201 (China); Wang Xuefei; Ouyang Qin; Chen Yousi; Yan Qing [National Engineering Laboratory of Carbon Fiber Preparation Technology, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201 (China)

    2012-10-15

    Highlights: Black-Right-Pointing-Pointer Longitudinal grooves on the fiber surface became more well-defined and much deeper after surface treatment. Black-Right-Pointing-Pointer The concentration of oxygen and nitrogen on the fiber surface increased after surface treatment. Black-Right-Pointing-Pointer The intensity of oxidative reaction varied with the change of ammonium-salt solutions. Black-Right-Pointing-Pointer The higher the concentration of OH{sup -} ions in the electrolytes, the violent the oxidative reaction happened. - Abstract: The surfaces of polyacrylonitrile-based carbon fibers were treated by an electrochemical anodic method. Three different kinds of ammonium-salt solutions namely NH{sub 4}HCO{sub 3}, (NH{sub 4}){sub 2}CO{sub 3} and (NH{sub 4}){sub 3}PO{sub 4} were respectively chosen as the electrolytes. The effect of these electrolytes on the surface structure was studied by scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). The results showed that longitudinal grooves on the fiber surface became more well-defined and much deeper after surface treatment, and the root mean square roughness (RMS) of carbon fiber surface increased from 4.6 nm for untreated fibers to 13.5 nm for treated fibers in (NH{sub 4}){sub 3}PO{sub 4} electrolytes. The concentration of oxygen and nitrogen atomic on the fiber surface increased after surface treatment. The tensile strength of oxidized fibers had an obvious decrease, whereas the interlaminar shear strength (ILSS) value of corresponding carbon fiber reinforced polymers (CFRPs) increased in a large extent. The intensity of oxidative reaction varied with the change of ammonium-salt solutions and electrochemical oxidation in (NH{sub 4}){sub 3}PO{sub 4} electrolyte was of the most violence. The corresponding mechanism was also discussed and the result showed that the higher the concentration of OH{sup -} ions in the electrolytes, the violent the oxidative

  9. Electrochemical reductions of Hg(II), ruthenium-nitrosyl complex, chromate, and nitrate in a strong alkaline solution

    International Nuclear Information System (INIS)

    The electrochemistry of low-level nuclear wastes, the reductions of Hg(II), [RuNO(NO2)4OH]2-, CrO42-, and NO3- in 1.33 M NaOH solution have been studied primarily at nickel electrodes for electrocatalytic advantages. Hg(II) was reduced to Hg metal [equilibrium potential of 0.099 V vs NHE (normal hydrogen electrode)]. The ruthenium-nitrosyl complex, [RuNO(NO2)4OH]2-, was reduced to Ru metal (half-wave potential of -0.38 V vs NHE). Chromate was reduced to chromic hydroxide (equilibrium potential of -0.24 V vs NHE). Nitrate reduction has two different regions of Tafel behavior from which reduction mechanisms are proposed. The exchange current densities for the nitrate reduction at Ni, Pb, Fe, and graphite were measured and the competition of the nitrate reduction with the hydrogen evolution investigated

  10. Results of Hg speciation testing on MCU strip effluent hold tank (SEHT) and decontaminated salt solution hold tank (DSSHT) materials

    Energy Technology Data Exchange (ETDEWEB)

    Bannochie, C. J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2015-09-17

    The Savannah River National Laboratory (SRNL) was tasked with preparing and shipping samples for Hg speciation by Eurofins Frontier Global Sciences, Inc. in Seattle, WA on behalf of the Savannah River Remediation (SRR) Mercury Task Team.i,ii The tenth shipment of samples was designated to include Modular Caustic Side Solvent Extraction Unit (MCU) Strip Effluent Hold Tank (SEHT) and MCU Decontaminated Salt Solution Hold Tank (DSSHT) materials from processing Salt Batch 7b. The MCU SEHT (MCU-15-722) and DSSHT (MCU-15-709) samples were pulled on June 15, 2015. All MCU samples were received at SRNL on June 16, 2015. The DSSHT sample was moved the same day to refrigeration, while the SEHT sample was placed in the Shielded Cells. On July 9, 2015 it was opened and an aliquot diluted 1:100 with Eurofins deionized water and a portion of the diluted sample transferred to a Teflon® bottle prior to moving it to refrigeration that same day. All samples were kept in the dark and refrigerated until final dilutions were prepared for shipment to Eurofins.

  11. Elaboration and test of the method of separation of alkaline metals ions with tin phosphate

    International Nuclear Information System (INIS)

    Present work is devoted to elaboration and test of the method of separation of alkaline metals ions with tin phosphate. Thus, the isotherms of sorption of lithium, sodium, potassium, rubidium and cesium ions with amorphous tin phosphate depending on their concentration, ph of solution, sorbent quantity are obtained. The parameters of extraction of potassium microquantities from sodium salts are defined. Ultra pure sodium chloride, sodium iodide, sodium sulphate, sodium nitrate, sodium nitrite, sodium phosphate are synthesized.

  12. Effect of salt identity on the phase diagram for a globularprotein in aqueous electrolyte solution

    Energy Technology Data Exchange (ETDEWEB)

    Bostrom, Mathias; Tavares, Frederico W.; Ninham, Barry W.; Prausnitz, John M.

    2006-02-22

    Monte Carlo simulations are used to establish the potential of mean force between two globular proteins in an aqueous electrolyte solution. This potential includes nonelectrostatic contributions arising from dispersion forces first, between the globular proteins, and second, between ions in solution and between each ion and the globular protein. These latter contributions are missing from standard models. The potential of mean force, obtained from simulation, is fitted to an analytic equation. Using our analytic potential of mean force and Barker-Henderson perturbation theory, we obtain phase diagrams for lysozyme solutions that include stable and metastable fluid-fluid and solid-fluid phases when the electrolyte is 0.2 M NaSCN or NaI or NaCl. The nature of the electrolyte has a significant effect on the phase diagram.

  13. Extraction concentration of scandium and rhenium from complex salt solutions containing low levels of valuable components

    International Nuclear Information System (INIS)

    The solutions under study contain 0.2 to 0.4 mg/l of scandium; 0.15 to 0.25 mg/l of rhenium and 1 to 3 g/l of iron. A solution of di-2-ethylhexylphosphoric acid and tributyl phosphate in kerosene was used as the extraction agent. The process takes place in a four-chamber instrument where the circulation of the extraction agent is provided. The iron content reduction is achieved by washing with a 200 g/l solution of sulfuric acid. Concentration values are achieved of 100 to 145 mg/l and 80 to 90 mg/l for scandium and rhenium, respectively. (M.D.). 6 tabs

  14. Experimental study of evaporation of horizontal films of water–salt solutions

    Directory of Open Access Journals (Sweden)

    Elistratov S.L.

    2015-01-01

    Full Text Available The present studies were carried out for the horizontal films (thin layers of water and water solutions of NaCl, CaCl2, LiCl, and LiBr with different solubility characteristics, as well as with specific features of formation and decay of water hydrates. Required volume of solution Vo of given weight concentration ξo, preliminary heated to the working surface temperature, was put in one step on the horizontal bottom of the bowl, heated to working temperature tCT, by means of volume batchers Thermo Scientific. After evaporation completion, the final mass of solution and form of their residue were registered. At the final stage of evaporation formation of NaCl crystals and water hydrates of CaCl2 · 2H2O, LiCl · H2O, and LiBr · 2H2O occurred.

  15. Copper-poly(2-aminodiphenylamine) as a novel and low cost electrocatalyst for electrocatalytic oxidation of methanol in alkaline solution

    Energy Technology Data Exchange (ETDEWEB)

    Ojani, Reza, E-mail: fer-o@umz.ac.i [Electroanalytical Chemistry Research Laboratory, Faculty of Chemistry, University of Mazandaran, Babolsar (Iran, Islamic Republic of); Raoof, Jahan-Bakhsh; Ahmady-Khanghah, Yusef [Electroanalytical Chemistry Research Laboratory, Faculty of Chemistry, University of Mazandaran, Babolsar (Iran, Islamic Republic of)

    2011-03-30

    In the present work we demonstrate the carbon paste as a new electrode substrate for the electropolymerization of 2-aminodiphenylamine and fabrication of polymer film modified electrode. Then transition metal of copper is incorporated into the polymer by electrodepositing of Cu(II) from CuCl{sub 2} acidic solution using potentiostatic technique. The electrocatalytic oxidation of methanol was studies by cyclic voltammetry and chronoamperometry methods at the surface of obtained Cu/P(2ADPA)/MCPE. It has been found that in the course of an anodic potential sweep, the electro-oxidation of methanol follows the formation of Cu(III) and is catalyzed by this species through a mediated electron transfer mechanism. The obtained current density for this catalytic oxidation is very high which could be come from high surface area of caused by the P(2ADPA) modification. The effects of various parameters such as the copper loading, scan rate and methanol concentration on the electrocatalytic oxidation of methanol were also investigated at the surface of Cu/P(2ADPA)/MCPE. Finally, using a chronoamperometric method, the catalytic rate constant (k) for methanol was found to be 0.2 x 10{sup 5} cm{sup 3} mol{sup -1} s{sup -1} that the high k can be ascribed for the fast electron transfer process due to electrode modification.

  16. Copper-poly(2-aminodiphenylamine) as a novel and low cost electrocatalyst for electrocatalytic oxidation of methanol in alkaline solution

    International Nuclear Information System (INIS)

    In the present work we demonstrate the carbon paste as a new electrode substrate for the electropolymerization of 2-aminodiphenylamine and fabrication of polymer film modified electrode. Then transition metal of copper is incorporated into the polymer by electrodepositing of Cu(II) from CuCl2 acidic solution using potentiostatic technique. The electrocatalytic oxidation of methanol was studies by cyclic voltammetry and chronoamperometry methods at the surface of obtained Cu/P(2ADPA)/MCPE. It has been found that in the course of an anodic potential sweep, the electro-oxidation of methanol follows the formation of Cu(III) and is catalyzed by this species through a mediated electron transfer mechanism. The obtained current density for this catalytic oxidation is very high which could be come from high surface area of caused by the P(2ADPA) modification. The effects of various parameters such as the copper loading, scan rate and methanol concentration on the electrocatalytic oxidation of methanol were also investigated at the surface of Cu/P(2ADPA)/MCPE. Finally, using a chronoamperometric method, the catalytic rate constant (k) for methanol was found to be 0.2 x 105 cm3 mol-1 s-1 that the high k can be ascribed for the fast electron transfer process due to electrode modification.

  17. Elution behavior of strontium from zeolite columns with inorganic salt and EDTA solutions

    International Nuclear Information System (INIS)

    The elution behavior of Sr sorbed on zeolite columns was investigated in connection with the distribution coefficient Kd between desired zeolites and aqueous solutions. The Kd values decreased with increasing concentrations of coexisting inorganic cations and EDTA. The retention volume VR on zeolite column was predicted from the Kd value. An EDTA solution was desirable for the quantitative elution of sorbed Sr from the column owing to the low Kd value reduced by complex formation with EDTA. The column efficiency and the elution percentage were improved with increasing temperature and decreasing flow rate. The structure of zeolite A remained unaltered after the repetitive use as the column packing. (author)

  18. Effect of salt solutions applied during wheat conditioning on lipase activity and lipid stability of whole wheat flour.

    Science.gov (United States)

    Doblado-Maldonado, Andrés F; Arndt, Elizabeth A; Rose, Devin J

    2013-09-01

    Lipolytic activity in whole wheat flour (WWF) is largely responsible for the loss in baking quality during storage. Metal ions affect the activity of seed lipases; however, no previous studies have applied this information to WWF in a way that reduces lipase activity, is practical for commercial manufacture, and uses common food ingredients. NaCl, KCl, Ca-propionate, or FeNa-ethylenediaminetetraacetic acid (FeNa-EDTA) were applied to hard red winter (HRW) and hard white spring (HWS) wheats during conditioning as aqueous solutions at concentrations that would be acceptable in baked goods. Salts affected lipase activity to different degrees depending on the type of wheat used. Inhibition was greater in HRW compared with HWS WWF, probably due to higher lipase activity in HRW wheat. In HRW WWF, 1% NaCl (flour weight) reduced hydrolytic and oxidative rancidity and resulted in higher loaf volume and lower firmness than untreated WWF after 24 weeks of storage. PMID:23578634

  19. Structural transformations of the synthetic salt 4`, 7-dihydroxyflavylium chloride in acid and basic aqueous solutions. Part 1-Ground state

    Energy Technology Data Exchange (ETDEWEB)

    Pina, F.; Benedito, L.; Melo, M.J.; Parola, A.J. [Centro de Quimica Fina e Biotecnologia. Departamento de Quimica FCT/UNL, Portugal (Portugal); Lima, J.C.; Macanita, A.L. [Instituto de Tecnologia Quimica e Biologica, Portugal (Portugal)

    1997-09-01

    A complete study of the structural pH dependent transformations of the synthetic flavylium salt 4`-7-dihydroxyflavylium chloride (DHF), occurring in aqueous solutions, including the basic region, is described. The kinetics study of the transformations occurring in acidic media (quinoidal base (A) {l_reversible} flavylium cation (AH{sup +}) {l_reversible} hemiacetal (B) {l_reversible} cis-chalcone (C-cis) {l_reversible} trans-chalcone (C-trans)) allowed to conclude that the cis-transisomerization is faster than the tautomerization and the hydration processes, which is unique in the anthocyanins family. Results obtained with the parent compound 4`-7-dimethoxyflavylium chloride (DMF)with relevance to this study are also presented. In equilibrated basic solutions the existence of acid-base equilibria involving the trans-Chalcone (C-trans) and its conjugated bases, (C-trans, and C``2-trans), was detected. Freshly prepared solutions at pH>7 show also the presence of a transient species identified as the ionized quinoidal base (A``-), which is almost completely converted into C``2-trans with a Ph dependent rate constant, (Author) 17 refs.

  20. Effect of plasticizer on surface of free films prepared from aqueous solutions of salts of cationic polymers with different plasticizers

    Science.gov (United States)

    Bajdik, János; Fehér, Máté; Pintye-Hódi, Klára

    2007-06-01

    Acquisition of a more detailed understanding of all technological processes is currently a relevant tendency in pharmaceutical technology and hence in industry. A knowledge of film formation from dispersion of polymers is very important during the coating of solid dosage forms. This process and the structure of the film can be influenced by different additives. In the present study, taste-masking films were prepared from aqueous citric acid solutions of a cationic polymer (Eudragit ® E PO) with various hydrophilic plasticizers (glycerol, propylene glycol and different poly(ethylene glycols)). The mechanical properties, film thickness, wetting properties and surface free energy of the free films were studied. The aim was to evaluate the properties of surface of free films to predict the arrangement of macromolecules in films formed from aqueous solutions of salts of cationic polymers. A high molecular weight of the plasticizer decreased the work of deformation. The surface free energy and the polarity were highest for the film without plasticizer; the hydrophilic additives decreased these parameters. The direction of the change in polarity (a hydrophilic component caused a decrease in the polarity) was unexpected. It can be explained by the change in orientation of the macromolecules, a hydrophobic surface being formed. Examination of the mechanical properties and film thickness can furnish additional results towards a knowledge of film formation by this not frequently applied type of polymer from aqueous solution.

  1. A study of substituent effect on the oxidative strengths of sodium salts of N-bromo-arylsulphonamides: Kinetics and mechanism of oxidation of D-fructose and D-glucose in alkaline medium

    Indian Academy of Sciences (India)

    K M Usha; B Thimme Gowda

    2006-07-01

    N-Bromo-arylsulphonamides of different oxidizing strengths are used for studying the kinetics of oxidation of D-fructose and D-glucose in aqueous alkaline medium. The results are analysed and compared with those from the sodium salts of N-bromo-benzenesulphonamide and N-bromo-4-methylbenzenesulphonamide. The reactions show zero-order kinetics in [oxidant], fractional order in [Fru/Glu] and nearly first order in [OH-]. Rates of oxidation of fructose are higher than those for glucose with the same oxidant. Similarly, values for glucose oxidations are higher than those for fructose. The results are explained by a suitable mechanism and the related rate law is deduced. The effective oxidising species in the reactions of N-bromo-arylsulphonamides is Br+. The oxidative strengths of the latter therefore depend on the ease with which Br+ is released from them. The ease with which Br+ is released from Nbromo- arylsulphonamides depends on the electron density on the nitrogen atom of the sulphonamide group, which in turn depends on the nature of the substituent on the benzene ring. The validity of the Hammett equation has also been tested for oxidation of both fructose and glucose. Enthalpies and entropies of activations of the oxidations by all the N-bromo-arylsulphonamides correlate well. The effect of substitution on and log of the oxidations is also considered.

  2. Ion Pairing in Aqueous Lithium Salt Solutions with Monovalent and Divalent Counter-Anions

    Czech Academy of Sciences Publication Activity Database

    Pluhařová, Eva; Mason, Philip E.; Jungwirth, Pavel

    2013-01-01

    Roč. 117, č. 46 (2013), s. 11766-11773. ISSN 1089-5639 R&D Projects: GA MŠk LH12001 Grant ostatní: MŠMT(CZ) LM2010005 Institutional support: RVO:61388963 Keywords : lithium * aqueous solution * neutron scattering * molecular dynamics * polarizability Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.775, year: 2013

  3. Sorption of thorium by alkylammonium salts of iso- and heteropolyacids of transition metals from aqueous solutions

    International Nuclear Information System (INIS)

    Results of investigations of thorium extraction from aqueous solutions by coprecipitation with water-repellent compounds, forming in direct interaction of 12-molybdophosphate heteropolyacid (HPA) with alkyltrimethylammoniumchloride, depending on the aqueous phase acidity are presented. It is established that degree of thorium extraction increases with an increase in the pH value and at transition to solutions with more diluted HPA. Thorium in hydrochloric acid media is extracted at a higher acidity of the aqueous phase in comparison with sulfuric acid media at the same concentration of HPA in the solution which is equal to 3.1x10-3 mol/l. Interaction of thorium with water-repellent precipitations proceeds due to processes of Th complexino. with HPA or HPA decomposition products. Data on infrared spectroscopic investigations of the composition of the water-repellent precipitations obtained under different conditions are presented. It is shown that the differences in the character of thorium distribution between precipitate and solution depend on the changes in the solid phase composition

  4. FTIR study of the photocatalytic degradation of gaseous benzene over UV-irradiated TiO2 nanoballs synthesized by hydrothermal treatment in alkaline solution

    International Nuclear Information System (INIS)

    In this study, photocatalysts of TiO2 nanoballs were obtained via a hydrothermal treating of commercial P25 in alkaline solution, and then characterized with SEM, XRD, BET and surface photovoltage spectroscopy techniques. The UV-assisted photodegradation of gaseous benzene over P25 and the prepared TiO2 nanoballs was monitored by an in situ infrared technique. The results demonstrated that the prepared TiO2 nanoballs in anatase form were more active than commercial P25 in photocatalytic oxidation of gaseous benzene. The promoted activity of the hydrothermal-treated TiO2 is attributed to the increasing specific surface area and larger band gap induced by the reduced crystallite size. The spectra of FTIR indicated that weakly adsorbed phenol was formed as the reaction progress. Hydroxyl groups on the surface of TiO2 nanoballs are able to react with photo-produced phenol, which is then retained on the catalyst surface leading to the progressive deactivation of the catalyst in the gas-solid system.

  5. Application of nano-sized nanoporous zinc 2-methylimidazole metal-organic framework for electrocatalytic oxidation of methanol in alkaline solution

    Science.gov (United States)

    Samadi-Maybodi, Abdolraouf; Ghasemi, Shahram; Ghaffari-Rad, Hamid

    2016-01-01

    In this work, a novel non-platinum group metals (non-PGM) catalyst based on modified zinc 2-methylimidazole metal-organic framework (ZIF-8) is proposed and used for electrooxidation of methanol. Nano-sized particles of nonporous ZIF-8 are synthesized at room temperature using a simple template-free method. The synthesized ZIF-8 nanoparticles are characterized by X-ray diffraction, scanning electronic microscopy and nitrogen adsorption-desorption techniques. In order to decrease the overvoltage of methanol oxidation on carbon paste electrode (CPE), nickel species doped ZIF-8 modified carbon paste electrode (Ni/ZIF-8CPE) is fabricated as a modified electrode. Electrochemical techniques such as cyclic voltammetry and chronoamperometry are used to investigate the electrocatalytic activity of Ni/ZIF-8CPE toward methanol oxidation in alkaline solution. Cyclic voltammetry results show that oxidation current is considerably increased using Ni/ZIF-8CPE in comparison with unmodified CPE. Catalytic rate constant of methanol oxidation on Ni/ZIF-8CPE is obtained using chronoamperometric studies. Besides the good catalytic activity of the modified electrode toward methanol oxidation, it has other advantages such as simple preparation, ease of operation, good stability and low cost, which can be promising in the field of preparation of non-PGM electrocatalysts for application in fuel cells.

  6. OSMOTIC DEHYDRATION KINETICS OF GUAVAS IN MALTOSE SOLUTIONS WITH CALCIUM SALT*

    Directory of Open Access Journals (Sweden)

    S. DI S. MASTRANTONIO

    2009-03-01

    Full Text Available

    The osmotic dehydration kinetics of guavas in maltose solutions at 40 and 60ºBrix, with addition of 0, 0.6 and 1.2% of calcium lactate was studied in this paper and the final product quality was evaluated. The experiments were carried out up to 60 hours and samples were taken for analysis at different times to evaluate guavas weight reduction, water loss and sugar gain and to characterize the product according to its texture and color. After 24 hours of process the mass transfer of water and sugar between the osmotic solution and the fruit was negligible, showing that process equilibrium was reached. The increase of sugar concentration in the osmotic solution showed strong influence on the dehydration process, increasing the water loss and reducing sugar gain. The presence of calcium ions in the osmotic solution also influenced the kinetics of mass transfer and showed a strong influence on fruit texture. Higher values of stress and strain at failure were obtained when calcium lactate was employed. The effect of the different osmotic treatments on the color parameters was also investigated and significant changes were observed in the values of chroma C* and hue H* due to sugar concentration and calcium addition.

    KEYWORDS: Osmotic dehydration; kinetics; guava; maltose; calcium lactate.

  7. Growth of lithium triborate single crystals from molten salt solution under various temperature gradients

    Science.gov (United States)

    Guretskii, S. A.; Ges, A. P.; Zhigunov, D. I.; Ignatenko, A. A.; Kalanda, N. A.; Kurnevich, L. A.; Luginets, A. M.; Milovanov, A. S.; Molchan, P. V.

    1995-12-01

    Single crystals of lithium triborate LiB 3O 5 (LBO) have been grown by the top-seeded solution growth method with B 2O 3 as a solvent using different temperature gradients in the zone of crystallization. Optical and nonlinear optical properties of LBO single crystals have been investigated. The influence of post-growth thermal treatment in oxygen atmosphere on the optical properties has been studied.

  8. Corrosion Tests of Steel Bar in Concrete under High Temperature by Salt Solution

    International Nuclear Information System (INIS)

    The saturation of South Korea's at-reactor (AR) spent fuel storage pools has created necessity for additional spent fuel storage capacity. The utility company (Korea Hydro and Nuclear Power Company) is planning to construct a dry storage facility, which offers advantages such as no generation of second time radioactive waste, relatively low operational cost, and a short construction period. Spent nuclear fuel from CANDU will be stored in MACSTOR-400. MACSTOR-400 developed by KHNP and AECL is a new dry storage module to replace Korea's existing concrete silo. This module composed of reinforced concrete has a capacity of 446MgU, twice the MACSTOR 200. Concrete has been used in the construction of nuclear facilities because of two primary properties, its structural strength and its ability to shield radiation. The use of concrete in nuclear facilities for containment and shielding of radiation and radioactive materials has made its performance crucial for the safe operation of the facility. Corrosion of reinforcing bars deteriorates the concrete structures and reduces their service life. Because spent fuel dry storage will be constructed near seashore, the reinforced concrete components and structures must withstand the damage due to salt attack under high temperature that is emitted by spent fuel. It can be noted that the temperature considerably affects degradation of reinforced concrete structure. However, there are very few examination examples to make clear the influence of the temperature. To obtain the basic material properties at high temperature and evaluate life time of spent fuel dry storage facility, the following test is now in progress

  9. OSMOTIC COEFFICIENTS, SOLUBILITIES, AND DELIQUESCENCE RELATIONS IN MIXED AQUEOUS SALT SOLUTIONS AT ELEVATED TEMPERATURE

    International Nuclear Information System (INIS)

    While thermodynamic properties of pure aqueous electrolytes are relatively well known at ambient temperature, there are far fewer data for binary systems extending to elevated temperatures and high concentrations. There is no general theoretically sound basis for prediction of the temperature dependence of ionic activities, and consequently temperature extrapolations based on ambient temperature data and empirical equations are uncertain and require empirical verification. Thermodynamic properties of mixed brines in a wide range of concentrations would enhance the understanding and precise modeling of the effects of deliquescence of initially dry solids in humid air in geological environments and in modeling the composition of waters during heating, cooling, evaporation or condensation processes. These conditions are of interest in the analysis of waters on metal surfaces at the proposed radioactive waste repository at Yucca Mountain, Nevada. The results obtained in this project will be useful for modeling the long-term evolution of the chemical environment, and this in turn is useful for the analysis of the corrosion of waste packages. In particular, there are few reliable experimental data available on the relationship between relative humidity and composition that reveals the eutonic points of the mixtures and the mixture deliquescence RH. The deliquescence RH for multicomponent mixtures is lower than that of pure component or binary solutions, but is not easy to predict quantitatively since the solutions are highly nonideal. In this work we used the ORNL low-temperature and high-temperature isopiestic facilities, capable of precise measurements of vapor pressure between ambient temperature and 250 C for determination of not only osmotic coefficients, but also solubilities and deliquescence points of aqueous mixed solutions in a range of temperatures. In addition to standard solutions of CaCl2, LiCl, and NaCl used as references, precise direct

  10. Nd:YAG laser associated with metal salts solutions in the treatment of dentinal hypersensitivity

    International Nuclear Information System (INIS)

    The objective of this study was to observe the ultrastructural changes caused by the radiation of Nd:YAG laser on the tooth tissue and determine qualitatively the presence of Sn++, Sr++ and F-, inside the dentin, being it irradiated or not. Ten molar teeth recently extracted were cut into 2 mm discs. The samples were soaked in a EDTA solution at 17% for 2 minutes and divided into five groups. Group I: the samples were irradiated with Nd:YAG laser (1,5 W, 100 mJ, 15 Hz, 150 μs and 125 J/cm2) and after that, a treatment with an SnF2 aqueous solution at 10% for 30 minutes. Group II: the samples got laser irradiation with the same parameters and then a treatment with an SrCl2 solution at 10% as a toothpaste (SensodyneTM) for 30 minutes. Group III: the samples just got a treatment with a SnF2 aqueous solution at 10% for 30 minutes. Group IV: the samples just got a treatment with a SrCl2 toothpaste (SensodyneTM) for 30 minutes. Group V: samples that just got laser irradiation in the parameters above mentioned. Then, all samples were prepared for scanning electronic microscopy (SEM) and the samples of groups I, II, III and IV for energy dispersive X-ray microanalysis (EDX). The ultrastructure aspect of the dentin showed the surface totally altered by the irradiation. Pits and whitish globules were found amidst an heterogenous and rough structure, due to the melting and resolidification of the dental structure. Craters were also observed. Carbonization areas were absent. Ions Sn++ were found at a depth of 250 μm in the samples of group I (Nd:YAG + SnF2), whereas in the samples of group III, Sn++ were not found deeper than 100 μm. Sr++ could be detected at least at 500 μm in the inner dentin in the samples of group II (Nd:YAG + SrCl2). However, Sn++ were not found at 50 μm in group IV samples. Ions F- were just found in the irradiated samples of group I. According to the study results we observed that through ultrastructural changes, caused by laser irradiation, a

  11. Influence of salt solutions on the swelling pressure and hydraulic conductivity of compacted GMZ01 bentonite

    OpenAIRE

    ZHU, Chunming; Ye, Wei-Min; Chen, Yong-Gui; Chen, Bao; Cui, Yu Jun

    2013-01-01

    During the long-term operation of a deep geological repository, infiltration of groundwater with different chemical compositions can affect the buffer/backfill properties of compacted bentonite. Using a newly developed apparatus, swelling pressure and permeability tests were carried out on densely compacted GMZ01 bentonite samples, which has an initial dry density of 1.70 Mg/m3, with de-ionized water as well as NaCl and CaCl2 solutions at different concentrations. Salinity effects of infiltra...

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

    International Nuclear Information System (INIS)

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

  13. Photoemission spectra of aqueous solutions of salts from many-body perturbation theory

    Science.gov (United States)

    Gaiduk, Alex P.; Skone, Jonathan H.; Govoni, Marco; Galli, Giulia

    The computational design of electrode materials for energy conversion and storage processes requires an accurate description of the energy levels of the electrolyte and of electrolyte/electrode interfaces. Conventional density-functional approximations are in general not well suited for this task as they yield inaccurate orbital energies. Many-body perturbation theory (MBPT) predicts vertical ionization potentials and energy gaps in better agreement with experiments, providing the possibility for an accurate description of the electronic properties of electrolytes. We coupled ab initio molecular dynamics with MBPT calculations to investigate the photoemission spectra of a 1 M aqueous solution of NaCl. For the first time we were able to determine the absolute positions of the spectra peaks, with excellent agreement with experiments for both the solute and solvent peak positions. The best results were obtained using wavefunctions obtained from dielectric-dependent hybrid calculations as a starting point for MBPT. Work supported by DOE BES DE-SC0008938. Computer time provided by the Argonne Leadership Computing Facility through the INCITE program.

  14. Influence of alkaline (PH 8.3-12.0) and saline solutions on chemical, mineralogical and physical properties of two different bentonites - batch experiments at 25 deg. C

    International Nuclear Information System (INIS)

    Document available in extended abstract form only. Construction of a spent fuel repository deep in the bedrock will need supporting structures using cement materials. A part of them can be removed before closure but still it is estimated that about 1000 tonnes will remain in the host rock. Degradation of cementitious materials produces leachates of high pH. If such an alkaline plume reaches the bentonite buffer, it may induce mineralogical and chemical changes in bentonite over long term, and further affect the safety functions of the buffer. Laboratory experiments were done with the objective to gain data of possible alterations in mineralogical, chemical and physical properties of bentonites contacted with high-pH saline solutions. Two untreated, high grade, Na- and Ca-bentonites, were used in batch experiments, which were carried out in an anaerobic glove-box at 25±1 deg. C for 554 days. Each bentonite sample (20 g) was leached with approximately 3.8 L of leaching solution, which equals 190 mL/g of bentonite. The bentonites were leached with three types of simulated cement waters (pH 9.7, 11.3 and 12.0) and one saline groundwater simulate (pH 8.3) as a reference. The leaching solutions were 0.3 M, and contained NaCl and CaCl2, and trace amounts of SiO2, K, Br, Mg and SO4. Dissolved oxygen and carbon dioxide were removed from leaching solutions before mixing of bentonite in PC bottles. The samples were placed on a platform shaker in order to allow better contact between bentonite and the leaching solution. The evolution of pH in the samples was followed by measuring the pH-value of each sample in the solution phase approximately twice a week and the solution was renewed when values of two to three consecutive measurements did not change. On average, the leaching solution was renewed once a month. For each renewal of the leaching solution the phases were separated, the reacted solution withdrawn, and the chemical composition analysed. Before analysis the

  15. Reductive extraction equilibrium of f-elements in the molten salt and liquid metal binary phase system

    International Nuclear Information System (INIS)

    Equilibrium distribution of lanthanides and actinides were experimentally determined in the binary phase system consisting of molten alkaline chloride salt and liquid metal. By analyzing the observed distribution ratio of solutes between salt phase and liquid Zn and Bi, thermodynamic constants of alloy formation of lanthanides and actinides with Zn and Bi were obtained. On the observed result, the systematics of lanthanides in their alloy formation with Zn and Bi was discussed and different systematics of actinides was discussed. (author)

  16. Equilibrium and dynamics of ionic solutions and molten salts: from the primitive model to molecular structures

    International Nuclear Information System (INIS)

    In this HDR (Accreditation to supervise researches) thesis, the author first recalls his research thesis work which addressed the study of structural properties of simple electrolyte solutions by neutron scattering and interpretation by using integral equations of statistic mechanics. He also evokes other related research works he supervised, and more recent research works he performed on a GDR Practis issue (the solubility of ionic compounds) in collaboration with German and Italian researchers. Thus, the author describes how his scientific activity has known a double evolution: on the experimental point of view (determination of scattering coefficients on long durations), and on the modelling point of view (transition from a model based on a continuous solvent to a model based on molecular structures, which meant a transition from integral equations of Brownian dynamics to a molecular dynamics)

  17. Quasi-elastic laser light scattering study of polyacrylamide hydrogel immersed in water and salt solutions

    Indian Academy of Sciences (India)

    M Sivanantham; B V R Tata

    2010-12-01

    Polyacrylamide (PAAm) hydrogels immersed in water and aqueous NaCl solutions were investigated for their structure and dynamics using static and quasi-elastic laser light scattering (QELS) techniques. Ensemble-averaged electric field correlation function (, ) obtained from the non-ergodic analysis of intensity-autocorrelation function for PAAm gel immersed in water and in 5 M NaCl showed an exponential decay to a plateau with an initial decay followed by saturation at long times. The value of the plateau was found to depend on NaCl concentration and was higher than that of water. Collective diffusion coefficient, , of the polymer network of the hydrogel immersed in water and in different concentrations of NaCl was determined by analysing (, ). The measured diffusion coefficient showed linear decrease with increase in concentration of NaCl. The characteristic network parameters were obtained by analyzing (, ) with harmonically bound Brownian particle model and from static light scattering studies.

  18. Tritium and excess heat generation during electrolysis of aqueous solutions of alkali salts with nickel cathode

    International Nuclear Information System (INIS)

    A number of open cell electrolysis experiments of the Mills and Kneizys type using Nickel as cathode, Pt wire as anode and aqueous solutions of carbonates of Potassium, Sodium and Lithium (natural and enriched) as electrolyte have been carried out in three different laboratories at Trombay. The cells were fabricated out of commercial dewar vacuum flasks. The difference in temperature at equilibrium between the operating cells and that of an identical dummy reference flask was measured to deduce excess heat. The cells were calibrated using resistance heaters. In all, studies have been carried out so far in 29 electrolytic cells with various electrolytes. In some cases a mixture of H2O and D2O was used. The cells were operated for a few weeks at a time and excess heat up to a maximum of 70% appears to be present in most cells when the input joule power is upto a watt or two. The current density was less than 40 mA/cm2. Electrolyte samples before and after electrolysis were analysed for tritium content after microdistillation to eliminate chemiluminescence effects. Samples from 18 out of 29 experiments analysed have indicated tritium levels varying in the region of 46 Bq/ml to 3390 Bq/ml. One cell with enriched Li2CO3 solution in H2O which was monitored continuously for over a month indicated that tritium generation is continuous. Although the highest amount of tritium produced so far was with a K2CO3 in 25% D2O cell, the generation of tritium in cells containing only H2O is a new finding. (author)

  19. Nd(III)/Cm(III) complexation with gluconate in NaCl and CaCl2 alkaline solutions: solubility and TRLFS studies

    International Nuclear Information System (INIS)

    Gluconic acid (GLU) is a poly-hydroxo-carboxylic acid expected in repositories for low and intermediate-level radioactive waste as a component of cementitious materials, added into the cement as water reducer and plasticiser. This work aims at assessing the solubility and aqueous speciation of An(III) and Ln(III) in the presence of GLU and dilute NaCl and CaCl2 solutions, as background electrolytes. Under-saturation solubility studies with Nd(OH)3(am) were conducted in inert gas (Ar) gloveboxes at (22±2) C. degrees. Samples were prepared in dilute NaCl (0.1 M) and CaCl2 (0.1 and 0.25 M) solutions as background electrolytes. Parallel experimental series were prepared with pHc = constant ≅ 12 and 10-6 M ≤ [GLU] ≤ 10-2 M, and with [GLU] = constant = 10-3 M and 9 ≤ pHc ≤ 13. TRLFS measurements were performed with [Cm(III)] ∼ 10-7 M per sample, and NaCl (0.1 M) and CaCl2 (0.1 and 0.25 M) as background electrolytes. Three different concentration levels of Ca2+ were considered in the NaCl systems: 0, 10-3 M and 10-2 M. The initial concentration of GLU in all samples (10-6 M) was increased to 3.10-3 M by step-wise additions of NaCl-NaGLU or CaCl2-CaGLU2 solutions of appropriate ionic strength. The solubility of Nd(OH)3(am) remained unaffected by GLU in 0.1 M NaCl solutions. On the other hand, the solubility of Nd(OH)3(am) in 0.1 and 0.25 M CaCl2 solutions was clearly increased by GLU under hyper-alkaline conditions. It was observed that the species forming are pH-dependent and unequivocally involve the participation of Ca2+, with the likely formation of a Nd-GLU complex with stoichiometry 1:2. No further increase of the Nd(III) concentration was observed at [GLU]tot ≥ 10-3 M, resulting in an upper solubility limit at [Nd] ∼ 10-6.5 M. This suggests the formation of a new Ca-Nd-GLU solubility limiting solid phase. Consistently with Nd(III) solubility data, TRLFS confirmed the key role of Ca2+ in the complexation process, with the likely formation of a Ca

  20. The diffusion behaviour of hydrogen in a low alloyed carbon steel with respect to the deformation level and to the passivation process in alkaline solutions

    International Nuclear Information System (INIS)

    The diffusion behaviour of hydrogen in a low alloyed carbon steel with respect to the deformation level and to the passivation process in alkaline solutions. The influence of plastic strain on the diffusion behaviour of hydrogen in a low alloyed structural steel (FeE 690T) was investigated using the electrochemical permeation technique. The plastic deformation was introduced either by cold rolling or by tensile straining. Specially prepared C(T)-specimen enabled the direct determination of the diffusion coefficient in the highly deformed region ahead of a blunting crack. It was shown, that the apparent diffusion coefficient depends on the plastic strain and on the overall hydrogen concentration, whereas the maximum hydrogen flux remained almost unchanged. These observations are interpreted in terms of variations in the dislocation density, which act as 'sinks' for the diffusable hydrogen atoms. The results are compared with model calculations, that describe the hydrogen transport as a function of the trap density. The comparison of the numerical simulation and the experimental data shows a good agreement over the whole range of plastic strain levels, leading to a trap density of 6.1.1019/d3. Together with the results of a previous study on the fracture toughness of FeE 690T in the presence of hydrogen the permeation data obtained in this work suggest that the observed influence of deformation rates on the fracture mechanism can be attributed to the reduced mobility of hydrogen atoms in the plastic zone. The assumption that the hydrogen transport during monotonic straining is controlled by diffusion was confirmed by investigations concerning the formation of surface films. Using a potentiodynamic method (cyclovoltammetry) a characterisation of the surface reactions involved in permeation experiments was performed. It was shown that the nature of the passive layers forming on the surface depends on the applied potential, affecting mainly the hydrogen absorption

  1. Orientation- and concentration-dependent surfactant adsorption on silicon in aqueous alkaline solutions: explaining the changes in the etch rate, roughness and undercutting for MEMS applications

    International Nuclear Information System (INIS)

    We combine spectroscopic ellipsometry (SE), Fourier transform infrared spectroscopy (FT-IR), kinetic Monte Carlo simulations (KMC) and convex corner undercutting analysis in order to characterize and explain the effect of the addition of small amounts of surfactant in alkaline aqueous solutions, such as Triton X-100 in tetra methyl ammonium hydroxide (TMAH). We propose that the surfactant is adsorbed at the silicon–etchant interface as a thin layer, acting as a filter that moderates the surface reactivity by reducing the amount of reactant molecules that reach the surface. According to the SE and FT-IR measurements, the thickness of the adsorbed layer is an orientation- and concentration-dependent quantity, mostly due to the orientation dependence of the surface density of H-terminations and the concentration dependence of the relative rates of the underlying oxidation and etching reactions, which have a direct impact on the number of OH terminations. For partial OH coverage of the surface, the hydration of the OH group effectively acts as an anchoring location for the hydration shell of a surfactant molecule, thus enabling the formation of hydration bridges that amplify the adsorption density of the surfactant. At high concentration, the model explains the large reduction in the etch rate of the exact and vicinal Si{1 1 0} surfaces, and the small changes in the etch rates for the exact and vicinal Si{1 0 0} surfaces. At low concentration, it explains how the etch rate for both families is significantly reduced. The orientation and concentration dependence of the surfactant adsorption explains the dramatic differences in the micron-scale wet-etched patterns obtained using TMAH and TMAH+Triton for microelectromechanical systems applications

  2. 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.

  3. Dissolution of nickel ferrite in aqueous solutions containing oxalic acid and ferrous salts

    International Nuclear Information System (INIS)

    The dissolution of nickel ferrite in oxalic acid and in ferrous oxalate-oxalic acid aqueous solution was studied. Nickel ferrite was synthesized by thermal decomposition of a mixed tartrate; the particles were shown to be coated with a thin ferric oxide layer. Dissolution takes place in two stages, the first one corresponding to the dissolution of the ferric oxide outer layer and the second one being the dissolution of Ni1.06Fe1.96O4. The kinetics of dissolution during this first stage is typical of ferric oxides: in oxalic acid, both a ligand-assisted and a redox mechanism operates, whereas in the presence of ferrous ions, redox catalysis leads to a faster dissolution. The rate dependence on both oxalic acid and on ferrous ion is described by the Langmuir-Hinshelwood equation. In the second stage, Langmuir-Hinshelwood kinetics also describes the dissolution of iron and nickel from nickel ferrite. It may be concluded that oxalic acid operates to dissolve iron, and the ensuing disruption of the solid framework accelerates the release of nickel

  4. Estudo eletroquímico de um novo banho galvânico de zinco alcalino livre de cianetos Electrochemical study of a novel cyanide free galvanic plating solution of alkaline zinc

    OpenAIRE

    Gecílio P. da Silva; Nacélio S. Freire; Diogo E. de Matos; Adriana N. Correia; Pedro de Lima-Neto

    2006-01-01

    A systematic electrochemical study of a novel cyanide free galvanic plating solution of alkaline zinc is presented. Cell Hull tests and potentiodynamic linear polarization measurements were carried out to evaluate the influence of operational parameters, such as concentration, current efficiency and degradation of additives. The stability of the bath was assessed by a long term test during 40 h at 200 A m-2. The morphology of the coatings was characterized by scanning electron microscopy. The...

  5. Electrochemical Investigations of Polycaprolactone-Coated AZ31 Mg Alloy in Earle's Balance Salt Solution and Conventional Simulated Body Fluid

    Science.gov (United States)

    Wilke, Benjamin M.; Zhang, Lei

    2016-06-01

    Polycaprolactone (PCL) coating has been shown to increase the corrosion resistance of magnesium alloys when exposed to a simulated body fluid. A PCL dip coating was applied to AZ31 Mg alloy. Samples were immersed in both Earle's Balance Salt Solution (EBSS) and conventional simulated body fluids (c-SBF) up to 14 days. Microscopic morphology, electrochemical impedance spectroscopy, and potentiodynamic polarization tests were performed to evaluate the corrosion behavior changes of PCL coatings against immersion times in EBSS and c-SBF as compared to the uncoated AZ31 substrate. PCL-coated samples demonstrated improved corrosion resistance compared to bare AZ31 in both EBSS and c-SBF, indicating that the PCL coating exhibited good corrosion protection of AZ31 in simulated body fluid. Samples immersed in EBSS showed significantly higher electrochemical impedance values and slower corrosion progression as compared to the samples in c-SBF, because of the decreased chloride content and CO2 buffering mechanism of the EBSS.

  6. Hank?s balanced salt solution: an alternative resuspension medium to label autologous leukocytes. Experience in inflammatory bowel disease

    Directory of Open Access Journals (Sweden)

    Martin-Comin Joseph

    2002-01-01

    Full Text Available In this work Hank's balanced salt solution (HBSS has been used, as resuspension medium, instead of leukocyte poor plasma (LPP to label autologous white blood cells in 28 patients with suspicion af active inflammatory bowel disease.Labelled cells were reinjected and anterior and caudo-craneal views were obtained at 30 min, 2 h and 6 h p.i. Regions of interest were outlined on liver, spleen, lung, bone marrow (spine, background and lesions and the organ/background activity ratios were calculated in all scans. Patients were classified into 2 groups: Group 1: LPP, 30 patients and Groups 2: HBSS, 28 patients. Labelling efficiency was higher in HBBS group (89.0 ± 3.2 % than in the LPP group (6.5 ± 6.3%. Organ/background activity ratios were similar in both groups. Concerning diagnostic accuracy was similar at 30 min and 2 h but the false positive rate increased at 6 h p.i. in the HBSS group. HBSS seems to be a valid alternative as resuspension medium in the labeling of autologous leukocytes but leukocyte poor plasma seem to induce less leukocyte damage. Based on these results, in our center HBSS is the currently used medium to label leukocytes.

  7. Atomistic molecular dynamics simulations of the structure of symmetric Polyelectrolyte block copolymer micelle in salt-free aqueous solution

    Science.gov (United States)

    Chockalingam, Rajalakshmi; Natarajan, Upendra

    2014-03-01

    The structure of a symmetric polystyrene- b - poly(acrylic acid) (PS- b - PAA) micelle in salt-free aqueous solution as a function of degree-of-neutralization (or ionization, f) of the PAA is studied via explicit-atom-ion MD simulations, for the first time for a polyelectrolyte block copolymer in a polar solvent. Micelle size increases with fin agreement with experimental observations in literature, due to extension of PAA at higher ionization. Pair RDF's with respect to water oxygens show that corona-water interaction becomes stronger with f due to an increase in number density of carboxylate (COO-) groups on the chain. Water-PAA coordination (carboxylate O's) increases with ionization. H-bonding between PAA and water increases with f due to greater extent of corona-water affinity. With increase in f, atom and counter-ion ρ profiles confirm extension of corona blocks and micelle existing in the ``osmotic regime,'' and a decrease in scattering peak intensity, in agreement with neutron scattering experiments and mean-field theory in literature. Inter-chain distance in PS core is found to decrease with ionization. Macromolecular Simulation and Modeling Laboratory, Dept. of Chemical Engineering, Indian Institute of Technology Madras, Chennai 600036.

  8. Obtainment of Hg-free Mn/Zn solutions from spent alkaline batteries; Obtencion de soluciones de Mn/Zn libres de Hg provenientes de pilas alcalinas gastadas

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Nicolas, L.; Espinosa-Ramirez, I. [Instituto Politecnico Nacional, UPALM, Mexico, D.F. (Mexico)]. E-mail: lepeni@hotmail.com; Aguilar, M. [Instituto de Fisica, UNAM, Mexico, D.F. (Mexico); Palacios-Beas, E. [Instituto Politecnico Nacional, UPALM, Mexico, D.F. (Mexico)

    2009-09-15

    As in many other countries, the excessive consumption of alkaline batteries in Mexico has generated highly contaminating wastes, with heavy metal contents such as Mn, Zn, Fe, Hg, Cu and Ni, among others. This has caused a large degree of environmental degradation with repercussions for the health of living beings. Because there are no regulations regarding the disposal of spent batteries, they are thrown out with the rest of the domestic wastes or directly into nature, ending up in open-air landfills or containers where they are incinerated, thereby contaminating the planet's environment, soil and springs. The present work studies the obtainment of solutions of Hg-free Mn and Zn (Mn/Zn {>=} 1) from spent alkaline batteries for use in synthesis of (Mn,Zn)Fe{sub 2}O{sub 4} ferrite by a wet method. The effect is analyzed of the dissolution medium (H{sub 2}SO{sub 4}/H{sub 2}O{sub 2}, HCl and HCl/NO{sub 3}) temperature and time on the percentage of dissolution of the metals present in the electrode material, characterized by atomic absorption (AA) spectroscopy and x-ray diffraction (XRD). The results of the investigation indicate that the best dissolution conditions are MD=H{sub 2}SO{sub 4}/H{sub 2}O{sub 2}, T=50 degrees Celsius and t =30 min, where 94.1 and 90.7 % (w/w) of Mn and Zn are obtained, respectively, with Mn/Zn = 1.51. The mercury content was determined to be 3.91%, higher than that stated by the battery specifications, which is recovered by dissolving with HCl/HNO{sub 3} in the residual solid. [Spanish] En Mexico como en muchos otros paises, el consumo excesivo de pilas alcalinas ha generado desechos altamente contaminantes, con contenidos de metales pesados como Mn, Zn, Fe, Hg, Cu y Ni entre otros, que han provocado un gran deterioro en el medio ambiente repercutiendo en la salud de los seres vivos. Dado que no se tiene una regulacion en cuanto a la disposicion de pilas gastadas, estas se desechan con el resto de las residuos domesticos o directamente

  9. Structure and thermodynamics of nonideal solutions of colloidal particles. Investigation of salt-free solutions of human serum albumin by using small-angle neutron scattering and Monte Carlo simulation

    DEFF Research Database (Denmark)

    Sjøberg, B.; Mortensen, K.

    1997-01-01

    Carlo simulation, to study salt-free solutions of human serum albumin (HSA) in the concentration range up to 0.26 g ml(-1). The model calculations of the theoretical SANS intensities are quite general, thus avoiding the approximation that the relative positions and orientations of the particles are...

  10. High-precision gigahertz-to-terahertz spectroscopy of aqueous salt solutions as a probe of the femtosecond-to-picosecond dynamics of liquid water

    CERN Document Server

    Vinh, N Q; Allen, S James; George, D K; Rahmani, A J; Plaxco, Kevin W

    2015-01-01

    Because it is sensitive to fluctuations occurring over femtoseconds to picoseconds, gigahertz-to-terahertz dielectric relaxation spectroscopy can provide a valuable window into water's most rapid intermolecular motions. In response, we have built a vector network analyzer dielectric spectrometer capable of measuring absorbance and index of refraction in this frequency regime with unprecedented precision. Using this to determine the complex dielectric response of water and aqueous salt solutions from 5.9 GHz to 1.12 THz (which we provide in the SI), we have obtained strong new constraints on theories of water's collective dynamics. For example, while the salt-dependencies we observe for water's two slower relaxations (8 and 1 ps) are easily reconciled with suggestions that they arise due to rotations of fully and partially hydrogen bonded molecules, respectively, the salt-dependence of the fastest relaxation (180 fs) appears difficult to reconcile with its prior assignment to liberations of single hydrogen bon...

  11. Catalytic decomposition of organic anions in alkaline radioactive wastes. 1. Oxidation of EDTA

    International Nuclear Information System (INIS)

    Decomposition of ethylenediaminetetraacetate in alkaline solutions by means of H2O2, Na2S2O8, NaClO, NaBrO is investigated by titrimetric method. It is established that EDTA is oxidized in heated over 60 Deg C solutions in the presence of cobalt salts in the case of step-by-step addition of H2O2 excess. Interaction of persulfate with EDTA is characterized by available induction period, which decreases with NaOH concentration, temperature increase and initial EDTA content decrease or in the presence of AgNO3, K4Fe(CN)6, NaNO2. Mechanism of the process includes thermal dissociation of persulfate ions on ion-radicals and following evolution of the chain reaction. Hypochlorite ions oxidize EDTA in 0.5-5.0 mol/l NaOH solutions in temperature range 25-60 Deg C. Efficiency of the process increases in the case of fractional addition of oxidizer in the presence of Co(II) or Ni(II) salts. EDTA oxidation in alkaline solutions by hypobromite ions takes place only in the case of temperature increase up to 95 Deg C. Co(II), Ni(II), Cu(II) salts accelerates the process

  12. Carbon dioxide solubility in aqueous potassium salt solutions of L-proline and DL-α-aminobutyric acid at high pressures

    International Nuclear Information System (INIS)

    Highlights: • CO2 solubility in aqueous potassium salt solutions of L-proline and DL-α-aminobutyric acid were studied. • The CO2 partial pressures studied was up to 1000 kPa. • The temperatures studied were (313.2, 333.2, 353.2) K. • The measured data were represented satisfactorily by using the applied correlations. • The CO2 absorption capacity of the studied systems was high and comparable with monoethanolamine. - Abstract: In the present work, the solubility of CO2 in aqueous solutions of potassium prolinate (KPr) and potassium α-aminobutyrate (KAABA) was measured at temperatures (313.2, 333.2, and 353.2) K and CO2 partial pressures up to 1000 kPa for amino acid salt concentrations: KPr, w = (7.5, 14.5, and 27.4 wt%) and KAABA, w = (6.9, 13.4, and 25.6 wt%). It was found that the CO2 absorption capacities of the studied amino acid salt systems were considerably high and comparable with that of industrially important alkanolamines including monoethanolamine. The CO2 loadings in aqueous potassium α-aminobutyrate at high pressures were also found to be generally higher than the loadings in aqueous potassium prolinate. A modified Kent–Eisenberg model was applied to correlate the CO2 solubility in the amino acid salt solution as function of CO2 partial pressure, temperature, and concentration. The model gave good representation of the (vapour + liquid) equilibrium data obtained for the amino acid salt systems studied, and provided accurate predictions of the solubility

  13. A balanced salt solution that prevents agglomeration of nano iron oxo-hydroxides in serum-free cellular assays

    Science.gov (United States)

    Pereira, Dora I. A.; Lederer, Bianca; Powell, Jonathan J.

    2015-01-01

    Nano iron oxo-hydroxides have numerous and increasing applications in biology and medicine. Assessment of their uptake and toxicity often requires cell culture but maintaining iron oxides uniformly nano-dispersed in such conditions can be challenging. We describe a balanced salt solution (BSS) compatible with cellular assays for use in such investigations. We determined hydrodynamic particle size and dispersibility of nano iron in BSS. The BSS, containing 130 mM NaCl, 10 mM KCl, 1 mM MgSO4, 5 mM glucose and 1.8 mM CaCl2 in 10 mM PIPES buffer (pH 7.4), was capable of maintaining nanoparticulate tartrate-modified Fe(III) oxo-hydroxide (i.e. nano Fe) mono-disperse (≥95% nanoparticulate) with a mean hydrodynamic particle diameter of 6.1 ± 0.3 nm. This size was similar to the native form of the nano Fe material (i.e. as synthesized) with a mean hydrodynamic particle diameter of 4.3 ± 0.1 nm in water. Furthermore, we show that BSS also adequately maintains nano Fe dispersion when supplemented with inhibitors of particle uptake or lysosomal acidification, namely chloropromazine and monensin, and when used at pHs 6.5 or 5.8. In conclusion, we provide a method for nanodispersion of iron oxo-hydroxides that is suitable for short term (1-3 h) cellular exposure investigations.

  14. A balanced salt solution that prevents agglomeration of nano iron oxo-hydroxides in serum-free cellular assays

    International Nuclear Information System (INIS)

    Nano iron oxo-hydroxides have numerous and increasing applications in biology and medicine. Assessment of their uptake and toxicity often requires cell culture but maintaining iron oxides uniformly nano-dispersed in such conditions can be challenging. We describe a balanced salt solution (BSS) compatible with cellular assays for use in such investigations. We determined hydrodynamic particle size and dispersibility of nano iron in BSS. The BSS, containing 130 mM NaCl, 10 mM KCl, 1 mM MgSO4, 5 mM glucose and 1.8 mM CaCl2 in 10 mM PIPES buffer (pH 7.4), was capable of maintaining nanoparticulate tartrate-modified Fe(III) oxo-hydroxide (i.e. nano Fe) mono-disperse (≥95% nanoparticulate) with a mean hydrodynamic particle diameter of 6.1 ± 0.3 nm. This size was similar to the native form of the nano Fe material (i.e. as synthesized) with a mean hydrodynamic particle diameter of 4.3 ± 0.1 nm in water. Furthermore, we show that BSS also adequately maintains nano Fe dispersion when supplemented with inhibitors of particle uptake or lysosomal acidification, namely chloropromazine and monensin, and when used at pHs 6.5 or 5.8. In conclusion, we provide a method for nanodispersion of iron oxo-hydroxides that is suitable for short term (1–3 h) cellular exposure investigations. (paper)

  15. De Novo Transcriptional Analysis of Alfalfa in Response to Saline-Alkaline Stress

    Science.gov (United States)

    An, Yi-Min; Song, Li-Li; Liu, Ying-Rui; Shu, Yong-Jun; Guo, Chang-Hong

    2016-01-01

    Saline-alkaline stress, caused by high levels of harmful carbonate salts and high soil pH, is a major abiotic stress that affects crop productivity. Alfalfa is a widely cultivated perennial forage legume with some tolerance to biotic and abiotic stresses, especially to saline-alkaline stress. To elucidate the mechanism underlying plant saline-alkaline tolerance, we conducted transcriptome analysis of whole alfalfa seedlings treated with saline-alkaline solutions for 0 day (control), 1 day (short-term treatment), and 7 days (long-term treatment) using ion torrent sequencing technology. A transcriptome database dataset of 53,853 unigenes was generated, and 2,286 and 2,233 genes were differentially expressed in the short-term and long-term treatment, respectively. Gene ontology analysis revealed 14 highly enriched pathways and demonstrated the differential response of metabolic pathways between the short-term and long-term treatment. The expression levels of 109 and 96 transcription factors were significantly altered significantly after 1 day and 7 days of treatment, respectively. Specific responses of peroxidase, flavonoids, and the light pathway component indicated that the antioxidant capacity was one of the central mechanisms of saline-alkaline stress tolerance response in alfalfa. Among the 18 differentially expressed genes examined by real time PCR, the expression levels of eight genes, including inositol transporter, DNA binding protein, raffinose synthase, ferritin, aldo/keto reductase, glutathione S-transferase, xyloglucan endotrans glucosylase, and a NAC transcription factor, exhibited different patterns in response to saline and alkaline stress. The expression levels of the NAC transcription factor and glutathione S-transferase were altered significantly under saline stress and saline-alkaline stress; they were upregulated under saline-alkaline stress and downregulated under salt stress. Physiology assays showed an increased concentration of reactive oxygen

  16. De Novo Transcriptional Analysis of Alfalfa in Response to Saline-Alkaline Stress.

    Science.gov (United States)

    An, Yi-Min; Song, Li-Li; Liu, Ying-Rui; Shu, Yong-Jun; Guo, Chang-Hong

    2016-01-01

    Saline-alkaline stress, caused by high levels of harmful carbonate salts and high soil pH, is a major abiotic stress that affects crop productivity. Alfalfa is a widely cultivated perennial forage legume with some tolerance to biotic and abiotic stresses, especially to saline-alkaline stress. To elucidate the mechanism underlying plant saline-alkaline tolerance, we conducted transcriptome analysis of whole alfalfa seedlings treated with saline-alkaline solutions for 0 day (control), 1 day (short-term treatment), and 7 days (long-term treatment) using ion torrent sequencing technology. A transcriptome database dataset of 53,853 unigenes was generated, and 2,286 and 2,233 genes were differentially expressed in the short-term and long-term treatment, respectively. Gene ontology analysis revealed 14 highly enriched pathways and demonstrated the differential response of metabolic pathways between the short-term and long-term treatment. The expression levels of 109 and 96 transcription factors were significantly altered significantly after 1 day and 7 days of treatment, respectively. Specific responses of peroxidase, flavonoids, and the light pathway component indicated that the antioxidant capacity was one of the central mechanisms of saline-alkaline stress tolerance response in alfalfa. Among the 18 differentially expressed genes examined by real time PCR, the expression levels of eight genes, including inositol transporter, DNA binding protein, raffinose synthase, ferritin, aldo/keto reductase, glutathione S-transferase, xyloglucan endotrans glucosylase, and a NAC transcription factor, exhibited different patterns in response to saline and alkaline stress. The expression levels of the NAC transcription factor and glutathione S-transferase were altered significantly under saline stress and saline-alkaline stress; they were upregulated under saline-alkaline stress and downregulated under salt stress. Physiology assays showed an increased concentration of reactive oxygen

  17. THE ADDITION OF CAFFEINE IN EARLE’S BALANCED SALT SOLUTION MEDIA WITH WASHING UP METHOD INCREASE MEMBRANE INTEGRITY AND ACROSOMAL SPERM

    OpenAIRE

    B. K. Satriyasa; and A. N. Mahendra

    2014-01-01

    Background: caffeine, a methylxanthine derivate, appears to inhibit phosphodiesterase, thereby inhibiting the break down of cAMP and increasing its concentration inside cell. This study aims to assess the effect of caffeine addition in Earles’s Balanced Salt Solution (EBSS) on the increase in membrane integrity and acrosome reaction of spermatozoa using swim up method. Methods: This study was carried out at the Clinic of Sexology and Andrology, Sanglah Public Hospital at Denpasar Bali-Indones...

  18. Marinade with alkaline solutions for the improvement of pork quality Marinados com soluções alcalinas para a melhoria da qualidade da carne suína

    Directory of Open Access Journals (Sweden)

    Viviane Maria Oliveira dos Santos

    2012-11-01

    Full Text Available The objective of this work was to evaluate the effects of alkaline solution marinades on the characteristics of pork subjected to post-mortem pH decrease in pig muscle. The pH of carcasses was measured in a commercial slaughterhouse (n = 526, 45 min after slaughtering (pH45 and, then, the carcasses were divided into the groups with pH455.7. Ten samples of the longissimus dorsi muscles of each group were collected and distributed in an entirely randomized design, in a 2x4 factorial arrangement, with two conditions (pH455.7, and four marinade solutions: TC, no marinade; TM1, sodium bicarbonate and sodium chloride; TM2, sodium tripolyphosphate and sodium chloride; TM3, sodium bicarbonate, sodium tripolyphosphate and sodium chloride. There was no interaction between pH45 of the meat and the marinade treatments. Meat with pH45O objetivo deste trabalho foi avaliar os efeitos de marinadas com soluções alcalinas sobre características da carne de porco submetida a quedas do pH post-mortem, em músculo de porco. O pH das carcaças foi medido em abatedouro comercial (n = 526, aos 45 min pós-abate (pH45 e, em seguida, as carcaças foram divididas em grupos com pH455,7. Dez amostras do músculo longissimus dorsi de cada grupo foram coletadas e distribuídas em delineamento inteiramente casualizado, em arranjo fatorial 2x4, com duas condições (pH455,7 e quatro soluções de marinação: TC, controle sem marinação; TM1, bicarbonato de sódio e cloreto de sódio; TM2, tripolifosfato de sódio e cloreto de sódio; TM3, bicarbonato de sódio, tripolifosfato de sódio e cloreto de sódio. Não houve interação entre o pH45 da carne e os tratamentos marinados. As carnes com pH45<5,7 apresentaram maior luminosidade, perda por purga (PP, perda de exsudato (PE, perda de peso por cozimento (PC e força de cisalhamento (FC. A marinação aumentou o pH da carne, reduziu a luminosidade, PE, PC e FC, e melhorou a maciez, suculência e palatabilidade. As marinadas

  19. Secretion of an alkaline protease from a salt- tolerant and alkaliphilic, Streptomyces clavuligerus strain Mit-1 Secreção de uma protease alcalina por uma cepa halotolerante e alcalifílica de Streptomyces clavuligerus, Mit-1

    Directory of Open Access Journals (Sweden)

    Jignasha T. Thumar

    2007-12-01

    Full Text Available An alkaliphilic and salt- tolerant actinomycete, Streptomyces clavuligerus strain Mit-1, was isolated from Mithapur, the western coast of India. The organism was Gram-positive, having filamentous, long thread like structure. The sporulation started after two days of growth and the optimum level of alkaline protease (130 U/ml was produced during the early stationary phase. The strain could grow and produce protease with 0-10% NaCl (w/v, the optimum being 5% NaCl (w/v. Growth and protease production was optimum at pH 9 with substantial decline at neutral pH. Sucrose and gelatin were the best carbon and nitrogen sources respectively, whereas gelatin broth was the preferred medium for protease production. Mit-1 produced substantial protease with various amino acids, when employed as the sole nitrogen sources. Crude substrates, such as molasses, whey and wheat flour had significant effect on enzyme production. The results are quite valuable, as only few actinomycetes, particularly salt-tolerant alkaliphilic ones, have so far been explored for their enzymatic potential and process optimization.Uma cepa halotolerante e alcalifílica de Streptomyces clavuligerus, Mit-1, foi isolada em Mithapur, na costa oeste da Índia. Esse microrganismo é Gram positivo e apresenta estrutura filamentosa na forma de longas cordas. A esporulação iniciou após dois dias de cultivo e o nível ótimo de produção de protease alcalina (130 U/ml foi atingido no início da fase estacionária de crescimento. A cepa foi capaz de multiplicar com 0-10% NaCl (w/v, com um ótimo de 5% NaCl (w/v. O ótimo de crescimento e produção de protease foi atingido em pH 9, apresentando declínio substancial em pH neutro. Sacarose e gelatina foram as melhores fones de carbono e nitrogênio, respectivamente, enquanto o caldo gelatina foi o melhor meio para produção de protease. A cepa Mit-1 produziu bastante protease quando vários aminoácidos foram empregados como única fonte de

  20. Thermodynamic study of aqueous solutions of polyelectrolytes of low and medium charge density without added salt by direct measurement of osmotic pressure

    International Nuclear Information System (INIS)

    A special block osmometer has been constructed and applied to a systematic study of poly (vinyl alcohol and vinyl sulphate ester) (PVS) sodium salts in dilute and moderately concentrated salt free aqueous solutions. In order to avoid surely ionic contamination all parts of the equipment that can contact with the polyelectrolyte solutions were made of different kinds of plastics and glass. The pressure range spans from (50 to 1.3 . 105) Pa. The measuring system was found to be appropriate for determination of the molar mass of water soluble polymers, too. Above a certain analytical density of dissociable groups (ADDG) an ion size dependent transition was observed on the reduced osmotic pressure vs. concentration curves. The analysis of the osmotic pressure data has clearly revealed that the dependence of the degree of dissociation on ADDG calculated at zero polyelectrolyte concentration contradicts to 'ion condensation' theory. With increasing polyelectrolyte concentration the degree of dissociation decreased rather steeply but at very low concentrations sharp maximums appeared due either to the change in conformation of these charged macromolecules, or formation of dynamic clusters induced by salting out of neutral parts of the macromolecules by the ionized groups. The applicability of the scaling concept as well as the many possible ways of characterization of non-ideality of polyelectrolyte solutions will be discussed in detail.

  1. Determination of fluorine by PIGE analysis on bovine tooth enamel treated with bamboo salt SMFP toothpaste and fluoride mouth rinsing solution

    International Nuclear Information System (INIS)

    The purpose of this study was to evaluate the effectiveness of a toothpaste containing bamboo salt on fluorine uptake in bovine enamel and to compare the efficiency of fluorine uptake between sodium monofluorophosphate(SMFP) toothpaste and sodium fluoride (NaF) mouthrinsing solution using proton induced γ-ray emission analysis. 30 bovine tooth enamel specimens were prepared and assigned to 5 groups as follows: specimens without any treatment, specimens which were treated with a toothpaste containing dicalcium phosphate dihydrate (DCPD) only, specimens which were treated with a toothpaste containing DCPD and SMFP, specimens which were treated with a toothpaste containing DCPD, SMFP and 2% bamboo salt, specimens which were treated with 0.05% NaF mouthrinsing solution. After 5 and 10 hours of treatment, fluorine concentration was measured at the depth of 263, 625, 2530 nm from the surface of the specimens. The surface concentration of fluorine was markedly increased using SMFP dentifrice. Bamboo salt did not encourage the uptake of fluorine into the enamel surface. NaF mouthrinsing solution showed a considerably higher uptake of fluoride in the intact enamel surface than the SMFP dentifrices. (author)

  2. Passivation behavior of Type 304 stainless steel in a non-aqueous alkyl carbonate solution containing LiPF{sub 6} salt

    Energy Technology Data Exchange (ETDEWEB)

    Myung, Seung-Taek [Department of Chemical Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate 020-8551 (Japan)], E-mail: smyung@iwate-u.ac.jp; Sasaki, Yusuke [Department of Chemical Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate 020-8551 (Japan); Saito, Takamitsu [Nissan Motors, 1 Natsushima, Yokosuka, Kanagawa 273-8523 (Japan); Sun, Yang-Kook [Department of Chemical Engineering, Hanyang University, Seungdong-Gu, Seoul 133-791 (Korea, Republic of); Yashiro, Hitoshi [Department of Chemical Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate 020-8551 (Japan)], E-mail: yashiro@iwate-u.ac.jp

    2009-10-01

    Passivation behavior of type 304 stainless steel in a non-aqueous alkyl carbonate solution containing LiPF{sub 6} salt was studied using electrochemical polarization, X-ray photoelectron spectroscopy (XPS) and time of flight-secondary ion mass spectroscopy (ToF-SIMS). Cathodic polarization to 0 V vs. Li/Li{sup +} resulted in most but not complete reduction of the air-formed film from oxides to metal on the stainless steel, as confirmed by XPS. For complete elimination of the air-formed film, the surface of the stainless steel was scratched under anodic polarization conditions. At 3 V vs. Li/Li{sup +} where an anodic current peak appeared, only an indistinct layer was recognized on the newly scratched surface, according to ToF-SIMS analysis. Above 4 V vs. Li/Li{sup +}, substantial passive films were formed, which were composed of oxides and fluorides of iron and chromium. The origin of oxide was due to water contained in the non-aqueous alkyl carbonate solution, and that of fluorides were the result of the decomposition of electrolytic salt, LiPF{sub 6}, especially at higher potential. The resultant passive films were stable in the non-aqueous alkyl carbonate solution containing LiPF{sub 6} salt.

  3. Effect of sodium phosphate salts on the thermodynamic properties of aqueous solutions of poly(ethylene oxide) 6000 at different temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Sadeghi, Rahmat [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)], E-mail: rahsadeghi@yahoo.com; Hosseini, Rahim; Jamehbozorg, Bahman [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)

    2008-09-15

    Precise density, sound velocity, water activity, and phase diagram measurements have been carried out on polyethylene oxide (PEO) in aqueous solutions of sodium di-hydrogen phosphate, di-sodium hydrogen phosphate, and tri-sodium phosphate over a range of temperatures at atmospheric pressure. The experimental density and sound velocity data are used to calculate the apparent specific volume and isentropic compressibility as a function of temperature and concentration. It was found that both of the apparent specific volume and isentropic compressibility of PEO in aqueous solutions increase by increasing temperature and charge on the anion of electrolytes. The results show that the slope of constant water activity lines increased with increasing the temperature and charge on the anion of electrolytes and the vapour pressure depression for an aqueous (PEO + sodium phosphate) system is more than the sum of those for the corresponding binary solutions. Furthermore, the effect of temperature and type of anion of salt on the salting-out effect of polyethylene oxide by sodium phosphate salts has been studied.

  4. Anditalea andensis ANESC-ST--An Alkaliphilic Halotolerant Bacterium Capable of Electricity Generation under Alkaline-Saline Conditions.

    Directory of Open Access Journals (Sweden)

    Wei Shi

    Full Text Available A great challenge in wastewater bioremediation is the sustained activity of viable microorganisms, which can contribute to the breakdown of waste contaminants, especially in alkaline pH conditions. Identification of extremophiles with bioremediation capability can improve the efficiency of wastewater treatment. Here, we report the discovery of an electrochemically active alkaliphilic halotolerant bacterium, Anditalea andensis ANESC-ST (=CICC10485T=NCCB 100412T, which is capable of generating bioelectricity in alkaline-saline conditions. A. andensis ANESC-ST was shown to grow in alkaline conditions between pH 7.0-11.0 and also under high salt condition (up to 4 wt% NaCl. Electrical output was further demonstrated in microbial fuel cells (MFCs with an average current density of ~0.5 µA/cm2, even under the harsh condition of 4 wt% NaCl and pH 9.0. Subsequent introduction of secreted extracellular metabolites into MFCs inoculated with Escherichia coli or Pseudomonas aeruginosa yielded enhanced electrical output. The ability of A. andensis ANESC-ST to generate energy under alkaline-saline conditions points towards a solution for bioelectricity recovery from alkaline-saline wastewater. This is the first report of A.andensis ANESC-ST producing bioelectricity at high salt concentration and pH.

  5. Anditalea andensis ANESC-ST--An Alkaliphilic Halotolerant Bacterium Capable of Electricity Generation under Alkaline-Saline Conditions.

    Science.gov (United States)

    Shi, Wei; Wang, Victor Bochuan; Zhao, Cui-E; Zhang, Qichun; Loo, Say Chye Joachim; Yang, Liang; Xu, Chenjie

    2015-01-01

    A great challenge in wastewater bioremediation is the sustained activity of viable microorganisms, which can contribute to the breakdown of waste contaminants, especially in alkaline pH conditions. Identification of extremophiles with bioremediation capability can improve the efficiency of wastewater treatment. Here, we report the discovery of an electrochemically active alkaliphilic halotolerant bacterium, Anditalea andensis ANESC-ST (=CICC10485T=NCCB 100412T), which is capable of generating bioelectricity in alkaline-saline conditions. A. andensis ANESC-ST was shown to grow in alkaline conditions between pH 7.0-11.0 and also under high salt condition (up to 4 wt% NaCl). Electrical output was further demonstrated in microbial fuel cells (MFCs) with an average current density of ~0.5 µA/cm2, even under the harsh condition of 4 wt% NaCl and pH 9.0. Subsequent introduction of secreted extracellular metabolites into MFCs inoculated with Escherichia coli or Pseudomonas aeruginosa yielded enhanced electrical output. The ability of A. andensis ANESC-ST to generate energy under alkaline-saline conditions points towards a solution for bioelectricity recovery from alkaline-saline wastewater. This is the first report of A.andensis ANESC-ST producing bioelectricity at high salt concentration and pH. PMID:26171779

  6. Alkaline flocculation of Phaeodactylum tricornutum induced by brucite and calcite

    OpenAIRE

    Vandamme, Dries; Pohl, Philip I.; Beuckels, Annelies; Foubert, Imogen; Brady, Patrick V.; Hewson, John C.; Muylaert, Koenraad

    2015-01-01

    Alkaline flocculation holds great potential as a low-cost harvesting method for marine microalgae biomass production. Alkaline flocculation is induced by an increase in pH and is related to precipitation of calcium and magnesium salts. In this study, we used the diatom Phaeodactylum tricornutum as model organism to study alkaline flocculation of marine microalgae cultured in seawater medium. Flocculation started when pH was increased to 10 and flocculation efficiency reached 90% when pH was 1...

  7. Specific Na+ and K+ Cation Effects on the Interfacial Water Molecules at the Air/Aqueous Salt Solution Interfaces Probed with Non-resonant Second Harmonic Generation (SHG)

    OpenAIRE

    Bian, Hong-tao; Feng, Ran-Ran; Guo, Yuan; Wang, Hong-fei

    2008-01-01

    Here we report the polarization dependent non-resonant second harmonic generation (SHG) measurement of the interfacial water molecules at the aqueous solution of the following salts: NaF, NaCl, NaBr, KF, KCl, and KBr. Through quantitative polarization analysis of the SHG data,the orientational parameter D value and the relative surface density of the interfacial water molecules at these aqueous solution surfaces were determined. From these results we found that addition of each of the six sal...

  8. Double blind, randomised controlled clinical trial of hypo-osmolar oral rehydration salt solution in dehydrating acute diarrhoea in severely malnourished (marasmic) children

    OpenAIRE

    Dutta, P; Mitra, U.; Manna, B.; Niyogi, S; K Roy; Mondal, C.; Bhattacharya, S.

    2001-01-01

    AIMS—To compare the clinical efficacy of hypo-osmolar oral rehydration salt (ORS) solution (224 mmol/l) and standard ORS solution (311 mmol/l) in severely malnourished (marasmic) children having less than 60% Harvard standard weight for age with dehydrating acute watery diarrhoea.
METHODS—In a double blind, randomised, controlled trial, 64 children aged 6-48 months were randomly assigned standard (n = 32) or hypo-osmolar ORS (n = 32).
RESULTS—Stool output (52.3 v 96.6 g/kg/day)...

  9. Experimental and molecular dynamics studies of dysprosium(III) salt solutions for a better representation of the microscopic features used within the binding mean spherical approximation theory

    International Nuclear Information System (INIS)

    This work is aimed at a predictive description of the thermodynamic properties of actinide (III) salt solutions at high concentration and 25 deg. C. A new solution of the binding mean spherical approximation (BIMSA) theory, based on the Wertheim formalism, for taking into account 1: 1 and also 1: 2 complex formation, is used to reproduce, from a simple procedure, experimental osmotic coefficient variation with concentration for three binary salt solutions of the same lanthanide (III) cation: dysprosium (III) perchlorate, nitrate, and chloride. The relevance of the fitted parameters is discussed, and their values are compared with available literature values. UV-vis/near-IR, time-resolved laser-induced fluorescence spectroscopy experiments, and molecular dynamics (MD) calculations were conducted for dilute to concentrated solutions (ca. 3 mol, kg-1) for a study of the microscopic behavior of DyCl3 binary solutions. Coupling MD calculations and extended X-ray absorption fine structure led to the determination of reliable distances. The MD results were used for a discussion of the parameters used in the BIMSA. (authors)

  10. Effect of the nature of alkali and alkaline-earth oxides on the structure and crystallization of an alumino-borosilicate glass developed to immobilize highly concentrated nuclear waste solutions

    International Nuclear Information System (INIS)

    A complex rare-earth rich alumino-borosilicate glass has been proved to be a good candidate for the immobilization of new high level radioactive wastes. A simplified seven-oxides composition of this glass was selected for this study. In this system, sodium and calcium cations were supposed in other works to simulate respectively all the other alkali (R+ = Li+, Rb+, Cs+) and alkaline-earth (R2+ = Sr2+, Ba2+) cations present in the complex glass composition. Moreover, neodymium or lanthanum are used here to simulate all the rare-earths and actinides occurring in waste solutions. In order to study the impact of the nature of R+ and R2+ cations on both glass structure and melt crystallization tendency during cooling, two glass series were prepared by replacing either Na+ or Ca2+ cations in the simplified glass by respectively (Li+, K+, Rb+, Cs+) or (Mg2+, Sr2+, Ba2+) cations. From these substitutions, it was established that alkali ions are preferentially involved in the charge compensation of (AlO4)- entities in the glass network comparatively to alkaline-earth ions. The glass compositions containing calcium give way to the crystallization of an apatite silicate phase bearing calcium and rare-earth ions. The melt crystallization tendency during cooling strongly varies with the nature of the alkaline-earth. (authors)

  11. Influence of Proton and Salt Concentration on the Chromonic Liquid Crystal Phase Diagram of Disodium Cromoglycate Solutions: Prospects and Limitations of a Host for DNA Nanostructures.

    Science.gov (United States)

    Zhang, Bingru; Kitzerow, Heinz-S

    2016-03-31

    Lyotropic chromonic liquid crystals have recently been suggested for use as a self-organized host for dispersing and aligning self-organized DNA origami nanostructures. However, an appropriate pH value and a suitable cation concentration are necessary to stabilize such nanostructures and to avoid unfolding of the DNA. The present study shows that the nematic and columnar liquid crystal phases appearing in aqueous solutions of disodium cromoglycate are robust against the replacement of deionized water by a neutral or alkaline buffer solution. However, disodium cromoglycate precipitates when an acidic buffer is used or when the concentration of magnesium cations exceeds a critical concentration of about 0.6-0.7 mmol/L. PMID:26964003

  12. Salt-effects in aqueous surface-active ionic liquid 1-dodecyl-3-methylimidazolium bromide solutions: Volumetric and compressibility property changes and critical aggregation concentration shifts

    International Nuclear Information System (INIS)

    Graphical abstract: Plot of ϕV against mIL, for solutions of [C12mim]Br in water (solid lines) and in aqueous solutions of 0.035 mol · kg−1 NaCl (dotted lines) at: ○ and ●, T = 288.15 K; △ and ▴,T = 293.15 K; □ and ■, T = 298.15 K. - Highlights: • Salt effect on the aggregation of [C12mim]Br in aqueous solutions were studied. • The effect of 6 chloride electrolytes and 5 sodium electrolytes were investigated. • Investigated electrolytes have salting-out effect on the aggregation of [C12mim]Br. • Changes in the volumes and compressibilities upon micellization were derived. - Abstract: Systematic studies on the volumetric and compressibility properties of aqueous solutions of model surface-active ionic liquid 1-dodecyl-3-methylimidazolium bromide ([C12mim]Br) are performed in the absence and presence of a large series of electrolytes in order to achieve a deeper understanding about the molecular mechanism behind the specific salt effect on the aggregation behavior of [C12mim]Br in aqueous solution. For this purpose, 6 chloride electrolytes (NaCl, KCl, NH4Cl, (CH3)4NCl, MgCl2 and FeCl3) and 5 sodium electrolytes (NaCl, NaNO3, Na2CO3, Na2SO4, and Na3Cit.) were used in order to individualize the effect of the anion and the cation. The values of the critical aggregation concentration (CAC) were obtained and it was found that all the investigated electrolytes have salting-out effect on the aggregation of [C12mim]Br in aqueous solutions, leading to significant downward shifts of the CAC. The magnitude of the shifts depends on the water-structuring nature of the electrolyte and follows the Hofmeister series. Changes in the apparent molar volumes and isentropic compressibilities upon micellization were derived using a pseudophase-transition approach and the infinite dilution apparent molar properties of the monomer and micellar form of [C12mim]Br were determined

  13. SANS study of micelle formation in aqueous mixed solutions of sodium and magnesium dodecylsulfates with added salts

    International Nuclear Information System (INIS)

    Complete text of publication follows. Mixtures of two anionic surfactants -sodium and magnesium didecyl sulphates- in heavy water were studied by small-angle neutron scattering (SANS) at various relative and total concentrations of the surfactants and various salt contents (NaCl and MgCl2). The average aggregation number and the effective fractional charge of mixed micelles were determined by fitting the data with the spherical or ellipsoidal shape model for the form factor and with the rescaled mean spherical approximation (RMSA) model for the structural factor. There are differences in the dependence of the characteristics of the mixed micelles formation on the relative concentration of the surfactants for the cases of their small and high total concentration. The changes in the micelle structure under salt addition are affected by the king of the salt. (author)

  14. Sobre os efeitos vasomotôres exercidos pela agua distilada e pelas soluções anisotonicas de clorêto de sodio Vaso-motricity induced by distilled water and anisotonic salt solutions

    Directory of Open Access Journals (Sweden)

    Antonio Augusto Xavier

    1939-01-01

    Full Text Available The writer reports experiments done with distilled water and hypotonic and hypertonic salt solutions of definite osmotic concentrations. The experiments were performed according to the Laewen-Trendelenburg technic using the vascular system of the frog's hind legs, and according to the Pissemski-Krawkow method using the capillaries of the rabbit's ear. Both preparations react to distilled water by marked vaso-constriction, the same phenomenon taking place in the case of the hypotonic salt solutions. The lower the concentration pf the hypotonic salt solution the stronger the vaso-constriction obtained. With hypertonic salt solutions was observed a strong but rather transient vaso-dilatation followed by secondary vaso-constriction. The later results were found only in the experiments with the frog's hind legs.

  15. Degradation of the herbicide 2, 4-dichlorophenoxyacetic acid (2,4-D) dimethylamine salt by gamma radiation from cobalt-60 in aqueous solution containing humic acid

    International Nuclear Information System (INIS)

    In this study, gamma radiation from cobalt-60 was used to degrade the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) dimethylamine salt in water in the presence of humic acid. The 2,4-D dimethylamine salt 1.13x10-4 mol dm-3 solution was irradiated with different doses. HPLC was used as an analytical technique to determine the degradation rate of herbicide studied. The results showed that the herbicide was completely degraded at an absorbed dose of 3 kGy. Degradation decreased when humic acid was added to all the doses. ESI/MS and MS/MS were used to identify the radiolytic degradation products. A fragmentation path for production of 4.6-dichlororesorcinol, is suggested. The radiolytic yields (G) were calculated

  16. Interdisciplinary studies on the long-term safety of an underground waste repository in salt rock in case of solution ingress. More precise definition of modelling requirements. Final report

    International Nuclear Information System (INIS)

    The study investigates how and to what extent numerical models will be able to describe the geomechanical, hydrological and geochemical effects and their interactions in the event of influx of solutions into potassium and salt rock shafts. Cause-and-effect mechanisms are discussed, taking into account mass transfer, dissolution processes, permeability, porosity, rock mechanics and stresses, hydraulic pressure, and reactions of solutions and salt rock. (DG)

  17. The salting-out effect and phase separation in aqueous solutions of tri-sodium citrate and 1-butyl-3-methylimidazolium bromide

    Energy Technology Data Exchange (ETDEWEB)

    Sadeghi, Rahmat, E-mail: rsadeghi@uok.ac.i [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of); Golabiazar, Roonak [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of); Shekaari, Hemayat [Department of Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of)

    2010-04-15

    The aim of this work is to obtain further evidence about the salting-out effect produced by the addition of tri-sodium citrate to aqueous solutions of water miscible ionic liquid 1-butyl-3-methylimidazolium bromide ([C{sub 4}mim][Br]) by evaluating the effect of tri-sodium citrate on the thermodynamic properties of aqueous solutions of this ionic liquid. Experimental measurements of density and sound velocity at different temperatures ranging from (288.15 to 308.15) K, the refractive index at 308.15 K and the liquid-liquid phase diagram at different temperatures ranging from (288.15 to 338.15) K for aqueous solutions containing 1-butyl-3-methylimidazolium bromide ([C{sub 4}mim][Br]) and tri-sodium citrate (Na{sub 3}Cit) are taken. The apparent molar volume of transfer of [C{sub 4}mim][Br] from water to aqueous solutions of Na{sub 3}Cit have positive values and it increases by increasing salt molality. Although at high IL molality, the apparent molar isentropic compressibility shows similar behaviour with that of the apparent molar volume. However at low concentrations of IL, the apparent molar isentropic compressibility of transfer of [C{sub 4}mim][Br] from water to aqueous solutions of Na{sub 3}Cit have negative values. The effects of temperature and the addition of Na{sub 3}Cit and [C{sub 4}mim][Br] on the liquid-liquid phase diagram of the investigated system have been studied. It was found that an increase in temperature caused the expansion of the one-phase region. The presence of Na{sub 3}Cit triggers a salting-out effect, leading to significant upward shifts of the liquid-liquid de-mixing temperatures of the system. The effect of temperature on the phase-forming ability in the system investigated has been studied based on a salting-out coefficient obtained from fitting the binodal values to a Setschenow-type equation for each temperature. Based on cloud point values, the energetics of the clouding process have been estimated and it was found that both of

  18. The salting-out effect and phase separation in aqueous solutions of tri-sodium citrate and 1-butyl-3-methylimidazolium bromide

    International Nuclear Information System (INIS)

    The aim of this work is to obtain further evidence about the salting-out effect produced by the addition of tri-sodium citrate to aqueous solutions of water miscible ionic liquid 1-butyl-3-methylimidazolium bromide ([C4mim][Br]) by evaluating the effect of tri-sodium citrate on the thermodynamic properties of aqueous solutions of this ionic liquid. Experimental measurements of density and sound velocity at different temperatures ranging from (288.15 to 308.15) K, the refractive index at 308.15 K and the liquid-liquid phase diagram at different temperatures ranging from (288.15 to 338.15) K for aqueous solutions containing 1-butyl-3-methylimidazolium bromide ([C4mim][Br]) and tri-sodium citrate (Na3Cit) are taken. The apparent molar volume of transfer of [C4mim][Br] from water to aqueous solutions of Na3Cit have positive values and it increases by increasing salt molality. Although at high IL molality, the apparent molar isentropic compressibility shows similar behaviour with that of the apparent molar volume. However at low concentrations of IL, the apparent molar isentropic compressibility of transfer of [C4mim][Br] from water to aqueous solutions of Na3Cit have negative values. The effects of temperature and the addition of Na3Cit and [C4mim][Br] on the liquid-liquid phase diagram of the investigated system have been studied. It was found that an increase in temperature caused the expansion of the one-phase region. The presence of Na3Cit triggers a salting-out effect, leading to significant upward shifts of the liquid-liquid de-mixing temperatures of the system. The effect of temperature on the phase-forming ability in the system investigated has been studied based on a salting-out coefficient obtained from fitting the binodal values to a Setschenow-type equation for each temperature. Based on cloud point values, the energetics of the clouding process have been estimated and it was found that both of entropy and enthalpy are the driving forces for biphasic

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

    Science.gov (United States)

    De Luca, R.

    2009-01-01

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

  20. Integrated membrane distillation-crystallization: process design and cost estimations for seawater treatment and fluxes of single salt solutions

    NARCIS (Netherlands)

    Creusen, R.J.M.; Medevoort, J. van; Roelands, C.P.M.; Renesse van Duivenbode, J.A.D. van; Hanemaaijer, J.H.; Leerdam, R.C. van

    2013-01-01

    The goal of this research is to design an integrated membrane distillation-crystallization (MDC) process for desalination of seawater with pure water and dry salts as the only products. The process is based on a combination of membrane distillation (MD) and osmotic distillation (OD) steps with integ