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Sample records for dilute aqueous salt

  1. Solubility and reactivity of peroxyacetyl nitrate (PAN) in dilute aqueous salt solutions and in sulphuric acid

    Science.gov (United States)

    Frenzel, A.; Kutsuna, S.; Takeuchi, K.; Ibusuki, T.

    The loss rates of PAN in several dilute aqueous salt solutions (NaBr, Na 2SO 3, KI, NaNO 2, FeCl 3, and FeSO 4) and in sulphuric acid were measured at 279 K with a simple bubbler experiment. They are little different from that in pure water. For 5 M sulphuric acid hydrolysis and solubility were determined in the temperature range of 243-293 K. The hydrolysis rate kh=3.2×10 -4 s -1 at 293 K is close to that in water. The observed temperature dependence of the Henry's Law constant H=10- 6.6±0.6exp((4780±420)/T) M atm -1 leads to enthalpy and entropy of solvation Δ Hsolv=-39.7±3.5 kJ mol -1 and Δ Ssolv=-126±11 J mol -1 K -1, respectively.

  2. Statistical mechanics of sum frequency generation spectroscopy for the liquid-vapor interface of dilute aqueous salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Noah-Vanhoucke, Joyce; Smith, Jared D.; Geissler, Phillip L.

    2009-01-02

    We demonstrate a theoretical description of vibrational sum frequency generation (SFG) at the boundary of aqueous electrolyte solutions. This approach identifies and exploits a simple relationship between SFG lineshapes and the statistics of molecular orientation and electric field. Our computer simulations indicate that orientational averages governing SFG susceptibility do not manifest ion-specific shifts in local electric field, but instead, ion-induced polarization of subsurface layers. Counterbalancing effects are obtained for monovalent anions and cations at the same depth. Ions held at different depths induce an imbalanced polarization, suggesting that ion-specific effects can arise from weak, long ranged influence on solvent organization.

  3. Statistical mechanics of sum frequency generation spectroscopy for the liquid-vapor interface of dilute aqueous salt solutions

    Science.gov (United States)

    Noah-Vanhoucke, Joyce; Smith, Jared D.; Geissler, Phillip L.

    2009-02-01

    We demonstrate a theoretical description of vibrational sum frequency generation (SFG) at the boundary of aqueous electrolyte solutions. This approach identifies and exploits a simple relationship between SFG lineshapes and the statistics of molecular orientation and electric field. Our computer simulations indicate that orientational averages governing SFG susceptibility do not manifest ion-specific shifts in local electric field, but instead, ion-induced polarization of subsurface layers. Counterbalancing effects are obtained for monovalent anions and cations at the same depth. Ions held at different depths induce an imbalanced polarization, suggesting that ion-specific effects can arise from weak, long-ranged influence on solvent organization.

  4. Terahertz absorption of dilute aqueous solutions.

    Science.gov (United States)

    Heyden, Matthias; Tobias, Douglas J; Matyushov, Dmitry V

    2012-12-21

    Absorption of terahertz (THz) radiation by aqueous solutions of large solutes reports on the polarization response of their hydration shells. This is because the dipolar relaxation of the solute is dynamically frozen at these frequencies, and most of the solute-induced absorption changes, apart from the expulsion of water, are caused by interfacial water. We propose a model expressing the dipolar response of solutions in terms of a single parameter, the interface dipole moment induced in the interfacial water by electromagnetic radiation. We apply this concept to experimental THz absorption of hydrated sugars, amino acids, and proteins. None of the solutes studied here follow the expectations of dielectric theories, which predict a negative projection of the interface dipole on the external electric field. We find that this prediction is not able to describe the available experimental data, which instead suggests a nearly zero interface dipole for sugars and a more diverse pattern for amino acids. Hydrophobic amino acids, similarly to sugars, give rise to near zero interface dipoles, while strongly hydrophilic ones are best described by a positive projection of the interface dipole on the external field. The sign of the interface dipole is connected to the slope of the absorption coefficient with the solute concentration. A positive slope, implying an increase in the solution polarity relative to water, mirrors results frequently reported for protein solutions. We therefore use molecular dynamics simulations of hydrated glucose and lambda repressor protein to calculate the interface dipole moments of these solutes and the concentration dependence of the THz absorption. The absorption at THz frequencies increases with increasing solute concentration in both cases, implying a higher polarity of the solution compared to bulk water. The structure of the hydration layer, extracted from simulations, is qualitatively similar in both cases, with spatial correlations

  5. Volatile release from aqueous solutions under dynamic headspace dilution conditions.

    Science.gov (United States)

    Marin, M; Baek, I; Taylor, A J

    1999-11-01

    Static equilibrium was established between the gas phase (headspace) and an unstirred aqueous phase in a sealed vessel. The headspace was then diluted with air to mimic the situation when a container of food is opened and the volatiles are diluted by the surrounding air. Because this first volatile signal can influence overall flavor perception, the parameters controlling volatile release under these conditions are of interest. A mechanistic model was developed and validated experimentally. Release of compounds depended on the air-water partition coefficient (K(aw)) and the mass transport in both phases. For compounds with K(aw) values 10(-)(3), mass transport in the gas phase became significant and the Reynolds number played a role. Because release from packaged foods occurs at low Reynolds numbers, whereas most experiments are conducted at medium to high Reynolds numbers, the experimentally defined profile may not reflect the real situation.

  6. [Influence of dissolved gases on highly diluted aqueous media].

    Science.gov (United States)

    Belovolova, L V; Glushkov, M V; Vinogradov, E A

    2014-01-01

    In the experiments on redox potential measurement for a series of identical samples of purified and presettled water it was found that the response to ultraviolet irradiation varies appreciably within a few days after treatment, including stepwise changes. In a few hours after exposure, leading to a higher content of reactive oxygen species as compared with the equilibrium values, long-term changes including variations in redox potential and optical system parameters are recorded in water and diluted aqueous media. We propose a heuristic organization model of the water-gas system with an increased content of reactive oxygen species.

  7. Dermal absorption of a dilute aqueous solution of malathion

    Directory of Open Access Journals (Sweden)

    Scharf John

    2008-01-01

    Full Text Available Malathion is an organophosphate pesticide commonly used on field crops, fruit trees, livestock, agriculture, and for mosquito and medfly control. Aerial applications can result in solubilized malathion in swimming pools and other recreational waters that may come into contact with human skin. To evaluate the human skin absorption of malathion for the assessment of risk associated with human exposures to aqueous solutions, human volunteers were selected and exposed to aqueous solutions of malathion. Participants submerged their arms and hands in twenty liters of dilute malathion solution in either a stagnant or stirred state. The "disappearance method" was applied by measuring malathion concentrations in the water before and after human exposure for various periods of time. No measurable skin absorption was detected in 42% of the participants; the remaining 58% of participants measured minimal absorbed doses of malathion. Analyzing these results through the Hazard Index model for recreational swimmer and bather exposure levels typically measured in contaminated swimming pools and surface waters after bait application indicated that these exposures are an order of magnitude less than a minimal dose known to result in a measurable change in acetylcholinesterase activity. It is concluded that exposure to aqueous malathion in recreational waters following aerial bait applications is not appreciably absorbed, does not result in an effective dose, and therefore is not a public health hazard.

  8. Electrical conductivity of aqueous solutions of aluminum salts

    Science.gov (United States)

    Vila, J.; Rilo, E.; Segade, L.; Cabeza, O.; Varela, L. M.

    2005-03-01

    We present experimental measurements of the specific electrical conductivity (σ) in aqueous solutions of aluminum salts at different temperatures, covering all salt concentrations from saturation to infinite dilution. The salts employed were AlCl3 , AlBr3 , AlI3 , and Al(NO3)3 , which present a 1:3 relationship between the electrical charges of anion and cation. In addition, we have measured the density in all ranges of concentrations of the four aqueous electrolyte solutions at 298.15K . The measured densities show an almost linear behavior with concentration, and we have fitted it to a second order polynomial with very high degree of approximation. The measurement of the specific conductivity at constant temperature reveals the existence of maxima in the conductivity vs concentration curves at molar concentrations around 1.5M for the three halide solutions studied, and at approximately 2M for the nitrate. We present a theoretical foundation for the existence of these maxima, based on the classical Debye-Hückel-Onsager hydrodynamic mean-field framework for electrical transport and its high concentration extensions, and also a brief consideration of ionic frictional coefficients using mode-coupling theory. We also found that the calculated values of the equivalent conductance vary in an approximately linear way with the square root of the concentration at concentrations as high as those where the maximum of σ appears. Finally, and for completeness, we have measured the temperature dependence of the electrical conductivity at selected concentrations from 283to353K , and performed a fit to an exponential equation of the Vogel-Fulcher-Tamman type. The values of the calculated temperatures of null mobility of the four salts are reported.

  9. Equilibrium sedimentation profile of dilute, salt-free charged colloids.

    Science.gov (United States)

    Wang, Tzu-Yu; Li, Hsien-Tsung; Sheng, Yu-Jane; Tsao, Heng-Kwong

    2008-11-28

    The sedimentation profile of a dilute colloidal solution follows the barometric distribution owing to the balance between gravitational force and thermal fluctuation. However, the electrostatic interactions may lead to significant deviation even in the low volume fraction limit (e.g., 10(-5)). On the basis of Monte Carlo simulations for a dilute, salt-free colloidal dispersion, five regimes can be identified through the resulting colloidal sedimentation profile and the counterion distribution. The electrostatic interactions depends on the Coulomb strength E(c) defined as the ratio of the Bjerrum length to the colloid size. At weak colloid-ion attractions (small E(c)), counterions tend to distribute uniformly in the container. However, both barometric and inflated profiles of colloids can be observed. On the contrary, at strong colloid-ion attraction (large E(c)), counterions accumulate in the vicinity of the colloids. Significant counterion condensation effectively decreases the strength of colloid-colloid repulsion and barometric profile of colloids can be obtained as well. As a result, the sedimentation profile and counterion distribution are indicative of the strength of effective colloid-colloid and colloid-ion interactions. It is also found that local electroneutrality condition is generally not satisfied and charge separation (or internal electric field) is neither a sufficient nor necessary condition for nonbarometric distributions.

  10. Monte Carlo Simulation of Aqueous Dilute Solutions of Polyhydric Alcohols

    Science.gov (United States)

    Lilly, Arnys Clifton, Jr.

    In order to investigate the details of hydrogen bonding and solution molecular conformation of complex alcohols in water, isobaric-isothermal Monte Carlo simulations were carried out on several systems. The solutes investigated were ethanol, ethylene glycol, 1,2-propylene glycol, 1,3 -propylene glycol and glycerol. In addition, propane, which does not hydrogen bond but does form water hydrates, was simulated in aqueous solution. The complex alcohol-water systems are very nonideal in their behavior as a function of solute concentration down to very dilute solutions. The water model employed was TIP4P water^1 and the intermolecular potentials employed are of the Jorgensen type^2 in which the interactions between the molecules are represented by interaction sites usually located on nuclei. The interactions are represented by a sum of Coulomb and Lennard-Jones terms between all intermolecular pairs of sites. Intramolecular rotations in the solute are modeled by torsional potential energy functions taken from ethanol, 1-propanol and 2-propanol for C-O and C-C bond rotations. Quasi-component pair correlation functions were used to analyze the hydrogen bonding. Hydrogen bonds were classified as proton acceptor and proton donor bonds by analyzing the nearest neighbor pair correlation function between hydroxyl oxygen and hydrogen and between solvent-water hydrogen and oxygen. The results obtained for partial molar heats of solution are more negative than experimental values by 3.0 to 14 kcal/mol. In solution, all solutes reached a contracted molecular geometry with the OH groups generally on one side of the molecule. There is a tendency for the solute OH groups to hydrogen bond with water, with more proton acceptor bonds than proton donor bonds. The water -solute binding energies correlate with experimental measurements of the water-binding properties of the solute. ftn ^1Jorgensen, W. L. et al, J. Chem. Phys., 79, 926 (1983). ^2Jorgensen, W. L., J. Phys Chem., 87, 5304

  11. Mössbauer spectroscopic studies of frozen aqueous solutions of Fe3+ salts

    DEFF Research Database (Denmark)

    Mørup, Steen; Knudsen, J. E.; Nielsen, M. K.

    1976-01-01

    Frozen aqueous solutions (FAS) of Fe3+ salts have been investigated by use of Mössbauer spectroscopy in order to study the conditions for formation of glasses. A general discussion of spin–spin relaxation in glasses is given, and we discuss how changes in the spin–spin relaxation time can...... concentration of the solution increases. At low temperatures the crystallization terminates and the remaining liquid solidifies into a glass. During exposure at 200 K, the dilute samples change irreversibly. This is discussed in terms of a metastable phase diagram. The properties of frozen solutions with other...

  12. SWELLING EQUILIBRIUM OF NONIONIC POLYACRYLAMIDE HYDROGEL IN AQUEOUS SALT SOLUTIONS

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A series of nonionic polyacrylamide hydrogels, using acrylamide as monomer and N,N’-methylene diacrylamide as crosslinking agent, were prepared by the free radical polymerization in aqueous solution. Swelling equilibria for the gels were carried out in aqueous solutions of NaCl, KCl, CaCl2, Na2HPO4 and K2HPO4 with concentration ranging from 10-3 to 5mol/kgH2O at 25℃. Experimental results revealed that the chlorides and phosphates cause a different behavior at higher salt concentration. The swelling ratio increases with increasing concentration of chlorides salts, while decreases with the increased phosphates salt concentration. The phenomena seem to be related to the different interactions of chloride and hydrogen phosphate ions with the network groups. Furthermore, the effects of different concentration of crosslinking agent and total monomers on gel swelling performance were also investigated.

  13. Temperature and concentration effects on the solvophobic solvation of methane in aqueous salt solutions.

    Science.gov (United States)

    Holzmann, Jörg; Ludwig, Ralf; Geiger, Alfons; Paschek, Dietmar

    2008-12-22

    We perform molecular dynamics (MD) simulations of aqueous salt (NaCl) solutions using the TIP4P-Ew water model (Horn et al., J. Chem. Phys. 2004, 120, 9665) covering broad temperature and concentration ranges extending deeply into the supercooled region. In particular we study the effect of temperature and salt concentration on the solvation of methane at infinite dilution. The salt effect on methane's solvation free energy, solvation enthalpy and entropy, as well as their temperature dependence is found to be semi-quantitatively in accordance with the data of Ben-Naim and Yaacobi (J. Phys. Chem. 1974, 78, 170). To distinguish the influence of local (in close proximity to ions) and global effects, we partition the salt solutions into ion influenced hydration shell regions and bulk water. The chemical potential of methane is systematically affected by the presence of salt in both sub volumes, emphasizing the importance of the global volume contraction due to electrostriction effects. This observation is correlated with systematic structural alterations similar to water under pressure. The observed electrostriction effects are found to become increasingly pronounced under cold (supercooled) conditions. We find that the influence of temperature and salt induced global density changes on the solvation properties of methane is well recovered by simple scaling relation based on predictions of the information theory model of Garde et al. (Phys. Rev. Let. 1999, 77, 4966).

  14. 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.

  15. Thermodynamics of multisolute adsorption from dilute aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Jossens, L. (Univ. Calif. Berkeley); Fritz, W.; Myers, A.L.; Prausnitz, J.M.; Schluender, E.U.

    1978-01-01

    Equilibrium adsorption data were obtained at 20/sup 0/C on activated carbon for six ternary aqueous systems simulating organic chemical wastewaters (phenol/p-nitrophenol, p-chlorophenol/p-nitrophenol, p-nitrophenol/benzoic acid, p-chlorophenol/phenyl acetic acid, o-phenylphenol/p-nitrophenol, and 2,4-dichlorophenol/dodecyl benzol sulfonic acid). The three-parameter Toth adsorption isotherm represented well the component single-solute data adsorption. With the thermodynamic ideal-adsorbed-solution method, total adsorptions were calculated from single-solute data predicted by the Toth equation and compared with experimental data. Prediction for total adsorption was within approx. 2-10Vertical Bar3<; for adsorption of individual components, within approx. 3-20Vertical Bar3<. A new three-parameter adsorption isotherm was derived, which also represented well the single-solute data. For bi-solute systems where dissociation is negligible, calculated individual adsorptions agreed with experiment within 2Vertical Bar3<. Systematic deviations between calculation and observed results may be due to the acidities of the solutes.

  16. Sonochemical degradation of organophosphorus pesticide in dilute aqueous solutions

    Institute of Scientific and Technical Information of China (English)

    Robina Farooq; FENG Kai-lin; S. F. Shaukat; HUANG Jian-jun

    2003-01-01

    Ultrasonic irradiation was found to accelerate the rate of hydrolysis of omethoate in aqueous solution over the pH range of 2-12. Process parameters studied include pH, steady-state temperature, concentration, and the type of gases. Greater than 96% hydrolysis was observed in 30 minutes through this process and the rate of destruction increased with the help of more soluble and low thermal inert gas. So with Krypton, omethoate was found to undergo rapid destruction as compared with Argon. In the presence of ultrasound, the observed first-order rate of hydrolysis of omethoate is found to be independent of pH. The formation of transient supercritical water(SCW) appears to be an important factor in the acceleration of chemical reactions in the presence of ultrasound. A detailed chemical reaction mechanism for omethoate destruction in water was formulated. Experimental results and theoretical kinetic mechanism demonstrated that the most of the omethoate undergo destruction inside the cavitating holes. A very less effect of temperature on the degradation of omethoate within a temperature range of 20-70℃ proves that a small quantity of omethoate undergoes secondary destruction in the bulk liquid.

  17. 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.

  18. Removal of transition metals from dilute aqueous solution by carboxylic acid group containing absorbent polymers

    Science.gov (United States)

    A new carboxylic acid group containing resin with cation exchange capacity, 12.67 meq/g has been used to remove Cu2+, Co2+ and Ni2+ ions from dilute aqueous solution. The resin has Cu2+, Co2+ and Ni2+ removal capacity, 216 mg/g, 154 mg/g and 180 mg/g, respectively. The selectivity of the resin to ...

  19. EFFECT OF RADIATION ON HIGH-CHARGE-DENSITY POLYDIALLY-DIMETHYL AMMONIUM CHLORIDE IN DILUTE AQUEOUS SOLUTION

    Institute of Scientific and Technical Information of China (English)

    Ya-long Zhang; Min Yi; Jing Ren; Hong-fei Ha

    2003-01-01

    The effect of radiation on high-charge-density cationic polymer, polydiallyl-dimethyl ammonium chloride (polyDADMAC), in dilute aqueous solution was investigated. The irradiated samples were characterized in terms of reduced viscosity and electric conductivity. The crosslinking reaction of polyDADMAC chains occurs preferentially in the irradiated samples at a concentration of polyDADMAC higher than 1.3 g/100 mL that was induced indirectly by the OH radicals, one of the radiolysis products of water. In more dilute samples (less than 0.8 g/100 mL) the chain scission of macro radicals appears to be the main reaction. N2O atmosphere enhances the erosslinking due to the extra OH radicals produced by reaction between N2O and eaq, another radiolysis products of water. Methanol and some mineral salts such as KC1, KBr inhibit the crosslinking to a certain extent. The mechanism of sensitization and inhibition is discussed in detail.

  20. Aqueous gel formation from sodium salts of cellobiose lipids.

    Science.gov (United States)

    Imura, Tomohiro; Yamamoto, Shuhei; Yamashita, Chikako; Taira, Toshiaki; Minamikawa, Hiroyuki; Morita, Tomotake; Kitamoto, Dai

    2014-01-01

    Cellobiose lipids (CLs) are asymmetric bolaform biosurfactants, which are produced by Cryptococcus humicola JCM 10251 and have fungicidal activity. In this study, the sodium salts of CLs (CLNa) were prepared to improve aqueous solubility of the CLs, and their surface and gelation properties in aqueous solutions were examined by surface tension, rheology, and freeze-fracture transmission electron microscopy (FF-TEM) measurements. The surface tension measurements revealed that the CLNa have high surface activity: CMC1 and γCMC1 are 0.1 mg/mL and 34.7 mN/m, respectively. It was also found that the CLNa form giant micelles above their CMC, whose average size is 116.6 ± 31.9 nm. Unlike conventional surfactants, the surface tension reduced further with an increase in concentration and the aqueous solution became viscous at the minimum gelation concentration (MGC: 5.0 mg/mL). In rheological studies, the obtained gels proved to be rather soft and their sol-gel temperature was found to be approximately 50℃. FF-TEM observation of the gels showed 3D supramolecular structures with an entangled fibrous network. Since the present CLNa aqueous gels have a degree of fungicidal activity, they could be useful for novel multifunctional soft materials applicable to the food and cosmetic industries.

  1. Discharge measurement with salt dilution method in irrigation canals: direct sampling and geophysical controls

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    C. Comina

    2013-08-01

    Full Text Available An important starting point for designing management improvements, particularly in irrigation areas, is to record the baseline state of the water resources, including the amount of discharge from canals. In this respect discharge measurements by means of the salt dilution method is a traditional and well-documented technique. However, this methodology can be strongly influenced by the natural streaming characteristics of the canal (e.g. laminar vs. turbulent flow and accurate precautions must be considered in the choice of both the measuring section and the length of the measuring reach of the canal which can affect the plume shape. The knowledge of plume distribution in the measuring cross-section is of primary importance for a correct location of sampling points aimed in obtaining a reliable measurement. To obtain this, geophysical imaging of an NaCl plume from a slug-injection salt dilution test has been performed within this paper by means of cross-flow fast electric resistivity tomography (FERT in a real case history. Direct sampling of the same plume has been also performed with a multisampling optimization technique to obtain an average value over the measuring section by means of contemporarily sampling water in nine points. Results show that a correct visualization of the passage of the salt plume is possible by means of geophysical controls and that this can potentially help in the correct location of sampling points.

  2. Counterion condensation of differently flexible polyelectrolytes in aqueous solutions in the dilute and semidilute regime.

    Science.gov (United States)

    Truzzolillo, D; Bordi, F; Cametti, C; Sennato, S

    2009-01-01

    The low-frequency limit of the electrical conductivity (dc conductivity) of differently flexible polyions in aqueous solutions has been measured over an extended polyion concentration range, covering both the dilute and semidilute (entangled and unentangled) regime, up to the concentrated regime. The data have been analyzed taking into account the different flexibility of the polymer chains according to the scaling theory of polyion solutions, in the case of flexible polyions, and according to the Manning model, in the case of rigid polyions. In both cases, the fraction f of free counterions, released into the aqueous phase from the ionizable polyion groups, has been evaluated and its dependence on the polyion concentration determined. Our results show that the counterion condensation follows at least three different regimes in dependence on the polyion concentration. The fraction f of free counterions remains constant only in the semidilute regime (a region that we have named the Manning regime), while there is a marked dependence on the polyion concentration both in the dilute and in the concentrated regime. These results are briefly discussed in the light of the scaling theory of polyelectrolyte aqueous solutions.

  3. Sepia 200cH at 1:1000 dilution ameliorates salt stress in cowpea seedlings but its medium 90% ethanol proves ineffective at the same dilution

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    Sandhimita Mondal

    2012-12-01

    Full Text Available Soil salinity severely affects crop yield all over the world. In a recent study we observed that Natrum mur 200cH, a homeopathic remedy, improved growth in germinating cowpea seeds. In the present study we have tested another remedy Sepia, which is complementary to Natrum mur, on cowpea seedlings under salt stress. Cowpea seedlings grown over moist filter paper in petridishes were divided into 4 groups: (1 control in sterile water, (2 in 50mM NaCl solution, (3 seeds pretreated with 90% ethanol diluted with water 1:100 and then transferred to 50mM NaCl solution, (4 seeds pretreated with Sepia 200cH diluted with water 1:100 and transferred to 50mM NaCl solution. In another experiment the groups were same, but the dilution of 90% ethanol and Sepia 200cH was 1:1000 instead of 1:100. The purpose was to further reduce the ethanol content in both the drug and its vehicle 90% ethanol, so that the alcohol effect is minimized or abolished. The data were analysed by ANOVA followed by t-test. Sepia 200cH at both 1:100 and 1:1000 dilutions significantly increased growth, sugar, chlorophyll, protein and water content in seedlings as compared to the untreated salt-stressed group. The effect with the1000th dilution of Sepia 200cH was more pronounced than with its 100th dilution. The vehicle 90% ethanol at 1:100 dilution produced some positive effect on the seedlings, but the 1000th dilution of the vehicle produced no such effect. It is, therefore, concluded that Sepia 200cH could ameliorate salt stress in cowpea seedlings and that the 1000th dilution is more effective than its 100th dilution. The alcohol effect is totally eliminated with the 1000th dilution of 90% ethanol. Thus the 1000th dilution could retain the drug effect and eliminate the vehicle effect.

  4. Efficient salt-aided aqueous extraction of bitter almond oil.

    Science.gov (United States)

    Liu, Lei; Yu, Xiuzhu; Zhao, Zhong; Xu, Lirong; Zhang, Rui

    2017-08-01

    Salt-aided aqueous extraction (SAAE) is an inexpensive and environmentally friendly method of oil extraction that is influenced by many factors. In the present study, we investigated the effect of SAAE on bitter almond oil yield. This study used sodium bicarbonate solution as extraction solvent and the optimal extraction parameters predicted by Box-Behnken design (i.e., concentration of sodium bicarbonate, 0.4 mol L(-1) ; solvent-to-sample ratio, 5:1; extraction temperature, 84 °C; extraction time, 60 min), for oil recovery of 90.9%. The physiochemical characteristics of the extracted oil suggest that the quality was similar to that of the aqueous enzymatic extracted oil. Moreover, the content of hydrocyanic acid (HCN) in bitter almond oil was found to be less than 5 mg kg(-1) , which was lower compared to that obtained by other reported methods. Results of microanalysis indicated that SAAE led to significant improvement in oil yield by allowing the release of oil and decreasing the emulsion fraction. Therefore, extraction of bitter almond oil by SAAE is feasible. These results demonstrate that extraction of bitter almond oil by SAAE based on the salt effect is feasible on a laboratory scale. © 2017 Society of Chemical Industry. © 2017 Society of Chemical Industry.

  5. Adsorption of organic acids from dilute aqueous solution onto activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Wang, S.W.

    1980-06-01

    The radioisotope technique was used to study the removal of organic acid contaminants from dilute aqueous solutions onto activated carbon. Acetic acid, propionic acid, n-butyric acid, n-hexanoic acid and n-heptanoic acid were studied at 278, 298, and 313/sup 0/K. Three bi-solute acid mixtures (acetic and propionic acids, acetic and butanoic acids, and propionic and butanoic acids) were studied at 278 and 298/sup 0/K. Isotherms of the single-solute systems were obtained at three different temperatures in the very dilute concentration region (less than 1% by weight). These data are very important in the prediction of bi-solute equilibrium data. A Polanyi-based competitive adsorption potential theory was used to predict the bi-solute equilibrium uptakes. Average errors between calculated and experimental data ranges from 4% to 14%. It was found that the competitive adsorption potential theory gives slightly better results than the ideal adsorbed solution theory.

  6. 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.

  7. Modeling of Pervaporation Separation Benzene from Dilute Aqueous Solutions Through Polydimethylsiloxane Membranes

    Institute of Scientific and Technical Information of China (English)

    彭福兵; 姜忠义

    2005-01-01

    A modified solution-diffusion model was established based on Flory-Huggins thermodynamic theory and Fujita's free volume theory. This model was used for description of the mass transfer of removal benzene from dilute aqueous solutions through polydimethylsiloxane (PDMS) membranes. The effect of component concentration on the interaction parameter between components, that of the polymer membrane on the selectivity to benzene, and that of feed concentration and temperature on the permeation flux and separation factor of benzene/water through PDMS membranes were investigated. Calculated pervaporation fluxes of benzene and water were compared with the experimental results and were in good agreement with the experimental data.

  8. Recovery of dilute acetone-butanol-ethanol (ABE) solvents from aqueous solutions via membrane distillation

    Energy Technology Data Exchange (ETDEWEB)

    Banat, F.A.; Al-Shannag, M. [Jordan Univ. of Science and Technology, Irbid (Jordan). Dept. of Chemical Engineering

    2000-12-01

    The simultaneous recovery of dilute acetone-butanol-ethanol (ABE) solvents from aqueous solutions by air gap membrane distillation was theoretically assessed. A previously developed and validated Stefan-Maxwell based mathematical model was used for this purpose. It was found that membrane distillation could successfully be used for the recovery of these solvents. Interestingly it was found that butanol could be separated with the highest selectivity and flux though it has the highest boiling point. The effect of operating conditions such as feed and cooling surface temperatures, air gap width, and individual component concentration on the flux and selectivity of these solvents was examined and discussed in this paper. (orig.)

  9. THE METHOD OF REMOVAL YTTRIUM (III AND YTTERBIUM (III FROM DILUTE AQUEOUS SOLUTIONS

    Directory of Open Access Journals (Sweden)

    Olga Lobacheva

    2016-04-01

    Full Text Available Yttrium (III and ytterbium (III cations ion flotation from diluted aqueous solutions in the presence of chloride ions using sodium dodecyl sulfate as collector agent were studied. Y (III and Yb (III distribution and recovery coefficients as a function of aqueous phase рН value at different sodium chloride concentrations were received. Yttrium (III and ytterbium (III chloro and hydroxo complexes instability constants were calculated. The calculation of separation coefficient at рН specified values depending on chloride ion concentration was conducted. Maximum separation coefficient was observed when chloride concentration of 0.01 M is 50 at рН 7.8. Ksep is minimal in nitrate medium ans is 3 at рН 7.0. At sodium chloride concentration of 0.05 М Ksep is 9 at рН 7.8.

  10. Influence of deacetylation on the rheological properties of xanthan-guar interactions in dilute aqueous solutions.

    Science.gov (United States)

    Khouryieh, H A; Herald, T J; Aramouni, F; Bean, S; Alavi, S

    2007-04-01

    An oscillating capillary rheometer was used to investigate the effects of xanthan deacetylation on the viscoelastic properties and intrinsic viscosity of xanthan and guar mixtures in dilute aqueous solutions. Deacetylated xanthan exhibited a stronger synergistic interaction with guar than native xanthan did due to the destabilized helical structure and increased chain flexibility of the deacetylated xanthan. No gels were observed for all xanthan-guar mixtures. Native xanthan-guar mixtures exhibited a liquid-like behavior, whereas deacetylated xanthan-guar mixtures exhibited a gel-like behavior. The relative viscosity and elasticity of deacetylated xanthan-guar mixtures were much stronger than those for native xanthan-guar mixtures. The intrinsic viscosities of deacetylated xanthan-guar mixtures were higher than the calculated values assuming no interaction, whereas the intrinsic viscosities of native xanthan-guar mixtures were lower than the calculated values assuming no interaction, demonstrating that intermolecular binding occurred between the disordered segments of xanthan and guar gum in dilute aqueous solutions.

  11. Effect of temperature on the dilution enthalpies of {alpha},{omega}-amino acids in aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Romero, C.M., E-mail: cmromeroi@unal.edu.co [Departamento de Quimica, Facultad de Ciencias, Universidad Nacional de Colombia, Bogota (Colombia); Cadena, J.C., E-mail: jccadena@unal.edu.co [Departamento de Quimica, Facultad de Ciencias, Universidad Nacional de Colombia, Bogota (Colombia); Lamprecht, I., E-mail: ingolf.lamprecht@t-online.de [Institut fuer Biologie, Freie Universitaet Berlin, Berlin (Germany)

    2011-10-15

    Highlights: > The dilution of 3-amino propanoic acid, 4-amino butanoic acid, 5-amino pentanoic acid, and 6-amino hexanoic acid in water is an exothermic process at T = (293.15, 298.15, 303.15, and 308.15) K. > The limiting experimental slopes of the enthalpies of dilution with respect to the molality change {Delta}m, are negative suggesting that the solutes interact with water primarily through their alkyl groups. > The value of the pairwise coefficient is positive at the temperatures considered, and the magnitude increases linearly with the number of methylene groups. > The comparison between the pairwise interaction coefficients for {alpha},{omega}-amino acids and {alpha}-amino acids shows that the change in the enthalpic interaction coefficient is related to the relative position of the polar groups. - Abstract: Dilution enthalpies of aqueous solutions of 3-amino propanoic acid, 4-amino butanoic acid, 5-amino pentanoic acid, and 6-amino hexanoic acid were determined at T = (293.15, 298.15, 303.15, and 308.15) K using an LKB flow microcalorimeter. The homotactic interaction coefficients were obtained according to the McMillan-Mayer theory from the experimental data. For all the systems studied, the dilution of {alpha},{omega}-amino acids in water is an exothermic process; the pair coefficients have positive values which increases with chain length. The obtained values of the interaction coefficients are interpreted in terms of solute-solvent and solute-solute interactions and are used as indicative of hydrophobic behavior of the amino acid studied.

  12. Aggregation and stability of anisotropic charged clay colloids in aqueous medium in the presence of salt.

    Science.gov (United States)

    Ali, Samim; Bandyopadhyay, Ranjini

    2016-01-01

    Na-montmorillonite nanoclay is a colloid of layered mineral silicate. When dispersed in water, this mineral swells on absorption of water and exfoliates into platelets with electric double layers on their surfaces. Even at low particle concentration, the aqueous dispersion can exhibit a spontaneous ergodicity breaking phase transition from a free flowing liquid to nonequilibrium, kinetically arrested and disordered states such as gels and glasses. In an earlier publication [Applied Clay Science, 2015, 114, 8592], we showed that the stability of clay gels can be enhanced by adding a salt later to the clay dispersion prepared in deionized water, rather than by adding the clay mineral to a previously mixed salt solution. Here, we directly track the collapsing interface of sedimenting clay gels using an optical method and show that adding salt after dispersing the clay mineral does indeed result in more stable gels even in very dilute dispersions. These weak gels are seen to exhibit a transient collapse after a finite delay time, a phenomenon observed previously in depletion gels. The velocity of the collapse oscillates with the age of the sample. However, the average velocity of collapse increases with sample age up to a peak value before decreasing at higher ages. With increasing salt concentration, the delay time for transient collapse decreases, while the peak value of the collapsing velocity increases. Using ultrasound attenuation spectroscopy, rheometry and cryogenic scanning electron microscopy, we confirm that morphological changes of the gel network assembly, facilitated by thermal fluctuations, lead to the observed collapse phenomenon. Since clay minerals are used extensively in polymer nanocomposites, as rheological modifiers, stabilizers and gas absorbents, we believe that the results reported in this work are extremely useful for several practical applications and also for understanding geophysical phenomena such as the formation and stability of quicksand

  13. Hydrogen bonding of single acetic acid with water molecules in dilute aqueous solutions

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    In separation processes,hydrogen bonding has a very significant effect on the efficiency of isolation of acetic acid (HOAc) from HOAc/H2O mixtures. This intermolecular interaction on aggregates composed of a single HOAc molecule and varying numbers of H2O molecules has been examined by using ab initio molecular dynamics simulations (AIMD) and quantum chemical calculations (QCC). Thermodynamic data in aqueous solution were obtained through the self-consistent reaction field calculations and the polarizable continuum model. The aggregation free energy of the aggregates in gas phase as well as in aqueous system shows that the 6-membered ring is the most favorable structure in both states. The relative stability of the ring structures inferred from the thermodynamic properties of the QCC is consistent with the ring distributions of the AIMD simulation. The study shows that in dilute aqueous solution of HOAc the more favorable molecular interaction is the hydrogen bonding between HOAc and H2O molecules,resulting in the separation of acetic acid from the HOAc/H2O mixtures with more difficulty than usual.

  14. Extraction and purification of anthraquinones derivatives from Aloe vera L. using alcohol/salt aqueous two-phase system.

    Science.gov (United States)

    Tan, Zhi-jian; Li, Fen-fang; Xu, Xue-lei

    2013-08-01

    An alcohol/salt aqueous two-phase system (ATPS) composed of 1-propanol and (NH4)2SO4 was employed to purify anthraquinones (AQs) extracted from Aloe vera L. The main influencing system parameters such as type of alcohol, type and concentration of salt, temperature and pH were investigated in detail. Under the optimal extraction conditions, AQs can be extracted into alcohol-rich phase with high extraction efficiency, meanwhile majority polysaccharides, proteins, mineral substances and other impurities were extracted into salt-rich phase. Partitioning of AQs is dependent on hydrophobic interaction, hydrogen bond interaction, and salting-out effect in ATPS. Temperature also played a great role in the partitioning. After ATPS extraction, alcohol can be recycled by evaporation; moreover, salt can be recycled by dilution crystallization method. Compared with other liquid-liquid extractions, this alcohol/salt system is much simpler, lower in cost with easier recovery of phase-forming components, which has the potential scale-up in down-processing of active ingredients in plant.

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

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Jun-Ho; Lim, Sohee; Chon, Bonghwan; Cho, Minhaeng, E-mail: mcho@korea.ac.kr [Center for Molecular Spectroscopy and Dynamics, Institute for Basic Science, Seoul 136-713 (Korea, Republic of); Department of Chemistry, Korea University, Seoul 136-713 (Korea, Republic of); Kim, Heejae; Kim, Seongheun [Department of Chemistry, Korea University, Seoul 136-713 (Korea, Republic of)

    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

  16. Crossover Leung-Griffiths model and the phase behavior of dilute aqueous ionic solutions

    Science.gov (United States)

    Belyakov, M. Yu.; Kiselev, S. B.; Rainwater, J. C.

    1997-08-01

    A new parametric crossover model for the phase behavior of a binary mixture is presented that corresponds to the Leung-Griffiths model in the critical region and is transformed into the regular classical expansion far away from the critical point. The model is optimized to, and leads to excellent agreement with, isothermal vapor-liquid equilibrium data for dilute aqueous solutions of sodium chloride by Bischoff and co-workers. It then accurately predicts constant-composition phase equilibrium loci as measured by independent workers. This crossover model is therefore capable of representing the thermodynamic surface of ionic solutions in a large range of temperatures and densities around the critical points of vapor-liquid equilibrium.

  17. Separation of glycols from dilute aqueous solutions via complexation with boronic acids

    Energy Technology Data Exchange (ETDEWEB)

    Randel, L.A.; King, C.J.

    1991-07-01

    This work examines methods of separating low molecular weight glycols from dilute aqueous solution. Extraction into conventional solvents is generally not economical, since, in the literature reviewed, distribution ratios for the two- to four-carbon glycols are all less than one. Distribution ratios can be increased, however, by incorporating into the organic phase an extracting agent that will complex with the solute of interest. The extracting agent investigated in this work is 3-nitrophenylboronic acid (NPBA). NPBA, a boric acid derivative, reversibly complexes with many glycols. The literature on complexation of borate and related compounds with glycols, including mechanistic data, measurement techniques, and applications to separation processes, provides information valuable for designing experiments with NPBA and is reviewed herein. 88 refs., 15 figs., 24 tabs.

  18. The Distribution of Plutonium(Ⅲ,Ⅳ) Nitrate Between Dilute TBP/OK and Aqueous Phase

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The distribution of plutonium (Ⅲ, Ⅳ) nitrate between dilute TBP/OK and aqueous phase is systematically investigated. On the basis of the preparation and stabilization of Pu(Ⅲ, Ⅳ), the influences of the concentration of HNO3, Al(NO3)3, TBP and UO2(NO3)2 on the distribution ratio of them are studied at 25℃. The results indicate that the distribution ratio of Pu(Ⅳ) has a maximum while that of Pu(Ⅲ) increases with the concentration of HNO3. The distribution ratio of Pu(Ⅲ, Ⅳ) increases along with the concentration of Al(NO3)3 and TBP. The extraction reaction

  19. Comparison of aqueous ammonia and dilute acid pretreatment of bamboo fractions: Structure properties and enzymatic hydrolysis.

    Science.gov (United States)

    Xin, Donglin; Yang, Zhong; Liu, Feng; Xu, Xueru; Zhang, Junhua

    2015-01-01

    The effect of two pretreatments methods, aqueous ammonia (SAA) and dilute acid (DA), on the chemical compositions, cellulose crystallinity, morphologic change, and enzymatic hydrolysis of bamboo fractions (bamboo yellow, timber, green, and knot) was compared. Bamboo fractions with SAA pretreatment had better hydrolysability than those with DA pretreatment. High crystallinity index resulted in low hydrolysis yield in the conversion of SAA pretreated bamboo fractions, not DA pretreated fractions. The increase of cellulase loading had modestly positive effect in the hydrolysis of both SAA and DA pretreated bamboo fractions, while supplement of xylanase significantly increased the hydrolysis of the pretreated bamboo fractions, especially after SAA pretreatment. The results indicated that SAA pretreatment was more effective than DA pretreatment in conversion of bamboo fractions, and supplementation of xylanase was necessary in effective conversion of the SAA pretreated fractions into fermentable sugars.

  20. Single chains of strong polyelectrolytes in aqueous solutions at extreme dilution: Conformation and counterion distribution

    Science.gov (United States)

    Xu, Guofeng; Luo, Shuangjiang; Yang, Qingbo; Yang, Jingfa; Zhao, Jiang

    2016-10-01

    The molecular conformation of two typical polyelectrolytes, sodium polystyrene sulfonate (NaPSS) and quarternized poly-4-vinylpyridine (QP4VP), was studied in aqueous solutions without salt addition at the single molecular level. By fluorescence correlation spectroscopy, the hydrodynamic radius (Rh) of NaPSS and QP4VP with the molecular weight ranging more than one order of magnitude was measured. The scaling analysis of Rh exhibits scaling exponent of 0.70 and 0.86 for NaPSS and QP4VP in solutions without added salts, respectively, showing the conformation is much more expanded than random coil. Numerical fittings using the model of diffusion of a rod molecule agree with the data well, indicating that the polyelectrolyte chains take the rod-like conformation under the condition without salt addition. Further investigations by determining the electric potential of single PSS- chains using the photon counting histogram technique demonstrate the enhanced counterion adsorption to the charged chain at higher molecular weight.

  1. Kinetics of the Reaction of CO2 with Aqueous Potassium Salt of Taurine and Glycine

    NARCIS (Netherlands)

    Kumar, P.S.; Hogendoorn, J.A.; Versteeg, G.F.; Feron, P.H.M.

    2003-01-01

    The kinetics of the reaction between CO2 and aqueous potassium salts of taurine and glycine was measured at 295 K in a stirred-cell reactor with a flat gas–liquid interface. For aqueous potassium taurate solutions, the temperature effect on the reaction kinetics was measured at 285 and 305 K. Unlike

  2. The solubility of toluene in aqueous salt solutions.

    Science.gov (United States)

    Poulson, S; Harrington, R; Drever, J

    1999-03-01

    The solubility of toluene has been measured in distilled water, and in various inorganic salt solutions. Values of the Setschenow constant, K(S), which quantify toluene solubility versus salt concentration, have been determined for each salt. Values of K(S) are compared to the activity of water for the salt solutions. Data from this study, consistent with earlier data, suggests that the effects of salts upon toluene solubility are non-additive. This contrasts the additive behavior of inorganic salts upon the solubility of nonpolar organic compounds, such as benzene and naphthalene, reported in the literature. Specific interaction between slightly polar toluene and ions in solution is suggested as a possible explanation for the non-additive effect of salts on the solubility of toluene.

  3. High-Yield Production of Levulinic Acid from Pretreated Cow Dung in Dilute Acid Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Jialei Su

    2017-02-01

    Full Text Available Agricultural waste cow dung was used as feedstock for the production of a high value–added chemical levulinic acid (LA in dilute acid aqueous solutions. A high LA yield of 338.9 g/kg was obtained from the pretreated cow dung, which was much higher than that obtained from the crude cow dung (135 g/kg, mainly attributed to the breakage of the lignin fraction in the lignocellulose structure of the cow dung by potassium hydroxide (KOH pretreatment, and thus enhanced the accessibility of cow dung to the acid sites in the catalytic reaction. Meanwhile, another value-added chemical formic acid could be obtained with a yield of ca. 160 g/kg in the process, implying a total production of ca. 500 g/kg yield for LA and formic acid from the pretreated cow dung with the proposed process. The developed process was shown to be tolerant to high initial substrate loading with a satisfied LA yield. This work provides a promising strategy for the value-increment utilization of liglocellulosic agricultural residues.

  4. Sequestration of chromium by exopolysaccharides of Nostoc and Gloeocapsa from dilute aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Mona [Department of Environmental Science and Engineering, Guru Jambheshwar University of Science and Technology, Hisar-125 001 (India); Kaushik, Anubha [Department of Environmental Science and Engineering, Guru Jambheshwar University of Science and Technology, Hisar-125 001 (India)], E-mail: aks_10@yahoo.com; Somvir,; Bala, Kiran; Kamra, Anjana [Department of Environmental Science and Engineering, Guru Jambheshwar University of Science and Technology, Hisar-125 001 (India)

    2008-09-15

    This article reports the chromium removal potential of exopolysaccharides (EPS) of two indigenously isolated cyanobacterial strains, Gloeocapsa calcarea and Nostoc punctiforme. The biosorption was studied by varying pH from 2 to 6 and initial chromium concentration from 5 to 20 mg/L to find out the optimized conditions for maximum chromium removal by EPS. Two equilibrium models, Langmuir and Freundlich, were used to explain these results. The Freundlich model was found to be better applicable to the experimental data as compared to Langmuir as inferred from high value of coefficient of determination whereas the optimal conditions were found to be same for the two (pH 2 and initial chromium concentration 20 mg/L). EPS production by the two strains was also studied which was found to be higher for Gloeocapsa. On the basis of experimental results and model parameters, it can be inferred that the EPS extracted from Nostoc has comparatively high biosorption capacity and can be utilized for the removal of chromium from dilute aqueous solution. Adsorption of chromium on EPS was further confirmed by surface morphology observed in scanning electron micrographs.

  5. An ab initio quantum mechanical charge field molecular dynamics simulation of a dilute aqueous HCl solution.

    Science.gov (United States)

    Kritayakornupong, Chinapong; Vchirawongkwin, Viwat; Rode, Bernd M

    2010-06-01

    An ab initio quantum mechanical charge field (QMCF) molecular dynamics simulation has been performed to study the structural and dynamical properties of a dilute aqueous HCl solution. The solute molecule HCl and its surrounding water molecules were treated at Hartree-Fock level in conjunction with Dunning double-zeta plus polarization function basis sets. The simulation predicts an average H-Cl bond distance of 1.28 A, which is in good agreement with the experimental value. The H(HCl)...O(w) and Cl(HCl)...H(w) distances of 1.84 and 3.51 A were found for the first hydration shell. At the hydrogen site of HCl, a single water molecule is the most preferred coordination, whereas an average coordination number of 12 water molecules of the full first shell was observed for the chloride site. The hydrogen bonding at the hydrogen site of HCl is weakened by proton transfer reactions and an associated lability of ligand binding. Two proton transfer processes were observed in the QMCF MD simulation, demonstrating acid dissociation of HCl. A weak structure-making/breaking effect of HCl in water is recognized from the mean residence times of 2.1 and 0.8 ps for ligands in the neighborhood of Cl and H sites of HCl, respectively. Copyright 2009 Wiley Periodicals, Inc.

  6. Lithium chloride ionic association in dilute aqueous solution: a constrained molecular dynamics study

    Science.gov (United States)

    Zhang, Zhigang; Duan, Zhenhao

    2004-02-01

    Constrained molecular dynamics simulations were carried out to investigate the lithium chloride ionic associations in dilute aqueous solutions over a wide temperature range. Solvent mediated potentials of mean force have been carefully calculated at different thermodynamic conditions. Two intermediate states of ionic association can be well identified with an energy barrier from the oscillatory free energy profile. Clear pictures for the microscopic association structures are presented with a remarkable feature of strong hydration effect of lithium ion and the bridging role of its hydrating complex. Experimental association constants have been reasonably reproduced and a general trend of the increasing ionic association at high temperatures and low densities was observed. Additional simulations with different numbers of water molecules have been performed to check the possible artifacts introducing from periodic and finite size effects and confirm the reliability of our simulation results. Marginal differences of the simulated curves are believed to result from the significant compensation and canceling effect between the bare ionic forces and solvent induced mean force. Finally we confirmed the importance of accurate descriptions of dielectric properties of solvent in the ionic association study.

  7. Selective flotation of zinc(II) and silver(I) ions from dilute aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Charewicz, W.A.; Holowiecka, B.A.; Walkowiak, W. [Wroclaw Univ. of Tech. (Poland)

    1999-09-01

    An experimental investigation is presented of the batch competitive flotation of zinc(II) and silver(I) ions from dilute aqueous solutions with sodium dodecylsulfate and ammonium tetradecysulfonate as anionic surfactants and with cetylpyridinium chloride as a cationic surfactant. The sequence of growing affinity of metal cations to anionic surfactants is the same as the sequence of ionic potential values of the studied cations: AG{sup +} < Zn{sup 2+}. The presence of potassium sulfate in aqueous solution has a negative influence of Zn{sup 2+} foam separation with a anionic surfactant which is due to competition for the surfactant between Zn{sup 2+} and K{sup +} cations. Also, the effect of inorganic ligands (i.e., thiosulfates, thiocyanates, and cyanides) on the selectivity of ion flotation of Zn(II) and Ag(I) is established. Results are discussed in terms of the complex species of zinc(II) and silver(I). At a total S{sub 2}O{sub 3}{sup 2{minus}} concentration of 3 {times} 10{sup {minus}6} M, the silver(I) is floated as a mixture of anions [Ag(S{sub 2}O{sub 3})]{sup {minus}} and [Ag(S{sub 2}O{sub 3}){sub 2}]{sup 3{minus}}, whereas zinc(II) remains in the aqueous phase as Zn{sup 2+}. At total concentrations of SCN{sup {minus}} from 1 {times} 10{sup {minus}4} to 2 {times} 10{sup {minus}3} M, silver(I) is floated as a mixture of [Ag(SCN){sub 2}]{sup {minus}} and AgSCN species. Partial separation of zinc(II) from silver(I) can be achieved in the presence of CN{sup {minus}} ligands at total concentrations varying from 2.5 {times} 10{sup {minus}4} to 1.0 {times} 10{sup {minus}3} M. The affinity of the studied cyanide complexes to cetylpyridinium chloride follows the order [Ag(CN){sub 2}]{sup {minus}} < [Zn(CN){sub 4}]{sup 2{minus}} + [Zn(CN){sub 3}]{sup {minus}}.

  8. Recovery of Cu(II from diluted aqueous solutions by non-dispersive solvent extraction

    Directory of Open Access Journals (Sweden)

    Alguacil, E. J.

    2002-08-01

    Full Text Available The removal of copper from diluted aqueous solutions with ACORGA M5640 extractant using non-dispersive solvent extraction technology was studied. It was possible to remove Cu(II below the international standars from solutions having initially as low concentration as 0,01 g/l under various experimental conditions, i.e aqueous pH 4.0, 10 % v/v ACORGA M5640 in Exxol D100, an organic flow of 100 ml/min, and an aqueous flow 50ml/min. Since the removal occurs by chelating ion exchange between copper from solution and protons from the extractant, the former was stripped by using a 180 g/l sulphuric acid solution which flowed (50 ml/min through the tube side organic was passed (400 ml/min through the shell side of the fibers of the module

    Se estudia la eliminación del cobre presente en disoluciones acuosas diluidas empleando el agente de extracción ACORGA M5640 y la tecnología de extracción con disolventes no dispersiva. Bajo las condiciones experimentales estudiadas, pH de la fase acuosa 4,0 ±0,1, 10 % v/v ACORGA M5640 en Exxsol D100, flujo de la fase orgánica 100 ml/min, flujo de la fase acuosa 50 ml/min, es posible eliminar el Cu(II, por debajo de los límites marcados internacionalmente, en disoluciones con un contenido tan bajo como 0,01 g/1 del metal. Debido a que la extracción transcurre mediante un intercambio catiónico (y formación de un compuesto tipo quelato entre el cobre presente en el medio acuoso y los protones del agente de extracción, el metal se puede reextraer mediante la utilización de una disolución de 180 g/1 de ácido sulfúrico que fluye (50 ml/min a través de la parte interior de las fibras del módulo, mientras que la fase orgánica fluye (400 ml/min por la parte exterior de las mismas fibras.

  9. Development of tropine-salt aqueous two-phase systems and removal of hydrophilic ionic liquids from aqueous solution.

    Science.gov (United States)

    Wu, Haoran; Yao, Shun; Qian, Guofei; Song, Hang

    2016-08-26

    A novel aqueous two-phase systems (ATPS) composed of a small molecule organic compound tropine and an organic or inorganic salt aqueous solution has been developed for the first time. The phase behavior of tropine-salt ATPS was systemically investigated and the phase equilibrium data were measured in different temperatures and concentrations and correlated by the Merchuk equation with satisfactory results. The detection of the conductivity and particle size proved the formation of micelle in the process of forming tropine-salt ATPS. The separation application of the ATPS was assessed with the removal of hydrophilic benzothiazolium-based ionic liquids (ILs) from aqueous solution. The result showed that ILs were effectively extracted into the top tropine-rich phase. Finally, ILs in the top tropine-rich phase were further separated by the means of adsorption-desorption with DM301 macroporous resin and ethanol. The method of novel tropine-salt ATPS combined with adsorption-desorption is demonstrated a promising alternative thought and approach for the removal or recovery of hydrophilic compounds from aqueous media and also could provide a potential application for bio-separation.

  10. Recovery of glycols, sugars, and Related Multiple -OH Compounds from Dilute-Aqueous Solution by Regenerable Adsorption onto Activated Carbons

    Energy Technology Data Exchange (ETDEWEB)

    Chinn, Daniel [Univ. of California, Berkeley, CA (United States)

    1999-06-01

    The present research explores the use of adsorption onto activated carbons as a means of recover glycerol, glycols, and sugars from dilute-aqueous solution. Our work is focused on understanding the mechanisms of adsorption onto carbons, assessing the degree of adsorption reversibility with precision, and implementing a bench-scale recovery process that results in a higher product concentration and reduction of the energy load for final purification.

  11. Forces between Hydrophobic Solids in Concentrated Aqueous Salt Solution

    OpenAIRE

    Mastropietro, Dean J; Ducker, William A.

    2012-01-01

    Much research has focused on the discovery and description of long-ranged forces between hydrophobic solids immersed in water. Here we show that the force between high contact-angle solids in concentrated salt solution (1 M KCl) agrees very well with van der Waals forces calculated from Lifshitz theory for separations greater than 5 nm. The hydrophobic solids are octadecyltrichlorosilane-coated glass, with an advancing contact angle of 108 degrees. Thus, in 1 M salt solution, it is unnecessar...

  12. Forces between hydrophobic solids in concentrated aqueous salt solution.

    Science.gov (United States)

    Mastropietro, Dean J; Ducker, William A

    2012-03-09

    Much research has focused on the discovery and description of long-ranged forces between hydrophobic solids immersed in water. Here we show that the force between high contact-angle solids in concentrated salt solution (1 M KCl) agrees very well with van der Waals forces calculated from Lifshitz theory for separations greater than 5 nm. The hydrophobic solids are octadecyltrichlorosilane-coated glass, with an advancing contact angle of 108°. Thus, in 1 M salt solution, it is unnecessary to invoke the presence of a hydrophobic force at separations greater than 5 nm. Through measurement in salt solution, we avoid the necessity of accounting for large electrostatic forces that frequently occur in pure water and may obscure resolution of other forces.

  13. Kinetics of absorption of carbon dioxide into aqueous potassium salt of proline

    DEFF Research Database (Denmark)

    Paul, Subham; Thomsen, Kaj

    2012-01-01

    The absorption of carbon dioxide (CO2) into aqueous solution of potassium prolinate (KPr) are studied at 303, 313, and 323K within the salt concentration range of 0.5–3.0kmolm−3 using a wetted wall column absorber. The experimental results are used to interpret the kinetics of the reaction of CO2...

  14. The potential/pH diagram of silver in aqueous ammonium salt solution

    NARCIS (Netherlands)

    Sluyters, J.H.; Wijnen, M.D.; Hul, H.J. van den

    1961-01-01

    The potential/pH diagram of silver in aqueous ammonium salt solution at 25°C has been calculated and verified experimentally. Calculations were carried out on the basis of the standard potential of the silver/silver-ion couple, the dissociation constants of the silver mono- and di-ammonia

  15. Effects of dilute aqueous NaCl solution on caffeine aggregation

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Bhanita; Paul, Sandip, E-mail: sandipp@iitg.ernet.in [Department of Chemistry, Indian Institute of Technology, Guwahati 781039, Assam (India)

    2013-11-21

    The effect of salt concentration on association properties of caffeine molecule was investigated by employing molecular dynamics simulations in isothermal-isobaric ensemble of eight caffeine molecules in pure water and three different salt (NaCl) concentrations, at 300 K temperature and 1 atm pressure. The concentration of caffeine was taken almost at the solubility limit. With increasing salt concentration, we observe enhancement of first peak height and appearance of a second peak in the caffeine-caffeine distribution function. Furthermore, our calculated solvent accessible area values and cluster structure analyses suggest formation of higher order caffeine cluster on addition of salt. The calculated hydrogen bond properties reveal that there is a modest decrease in the average number of water-caffeine hydrogen bonds on addition of NaCl salt. Also observed are: (i) decrease in probability of salt contact ion pair as well as decrease in the solvent separated ion pair formation with increasing salt concentration, (ii) a modest second shell collapse in the water structure, and (iii) dehydration of hydrophobic atomic sites of caffeine on addition of NaCl.

  16. Effects of dilute aqueous NaCl solution on caffeine aggregation

    Science.gov (United States)

    Sharma, Bhanita; Paul, Sandip

    2013-11-01

    The effect of salt concentration on association properties of caffeine molecule was investigated by employing molecular dynamics simulations in isothermal-isobaric ensemble of eight caffeine molecules in pure water and three different salt (NaCl) concentrations, at 300 K temperature and 1 atm pressure. The concentration of caffeine was taken almost at the solubility limit. With increasing salt concentration, we observe enhancement of first peak height and appearance of a second peak in the caffeine-caffeine distribution function. Furthermore, our calculated solvent accessible area values and cluster structure analyses suggest formation of higher order caffeine cluster on addition of salt. The calculated hydrogen bond properties reveal that there is a modest decrease in the average number of water-caffeine hydrogen bonds on addition of NaCl salt. Also observed are: (i) decrease in probability of salt contact ion pair as well as decrease in the solvent separated ion pair formation with increasing salt concentration, (ii) a modest second shell collapse in the water structure, and (iii) dehydration of hydrophobic atomic sites of caffeine on addition of NaCl.

  17. Ionic Liquid-salt Aqueous Two-phase System, a Novel System for the Extraction of Abused Drugs

    Institute of Scientific and Technical Information of China (English)

    She Hong LI; Chi Yang HE; Hu Wei LIU; Ke An LI; Feng LIU

    2005-01-01

    A 1-butyl-3-methylimidazolium chloride-salt aqueous two-phase system was studied on extraction of abused drugs. The effects of sorts of salts, temperature, concentration of salt and drugs on system were investigated systematically. A satisfactory extraction efficiency of 93%was obtained for papaverine while that of morphine was 65%. The extraction mechanism was primarily discussed.

  18. Capacitance of porous carbon electrode in mixed salt non-aqueous electrolytes

    Science.gov (United States)

    Egashira, Minato; Sawada, Nozomu; Ueda, Kazuteru; Yoshimoto, Nobuko; Morita, Masayuki

    Capacitances of a porous carbon electrode in non-aqueous electrolytes containing tetraethylamonium tetrafluoroborate (TEABF 4) and a lithium salt with various compositions have been investigated for the potential use in electric double layer capacitor. In the electrolyte prepared by dissolving TEABF 4 and LiBF 4 into the mixed solvent of ethylene carbonate (EC) with diethyl carbonate (DMC), an activated carbon fiber (ACF) electrode exhibits a larger capacitance than in TEABF 4 single salt electrolyte on cyclic voltammograms. The symmetrical capacitor cell containing the LiBF 4-TEABF 4 mixed salt electrolyte also exhibits larger capacitance on a constant-current test compared with that containing the TEABF 4 single salt electrolyte, while the capacitance degradation is observable for this cell at a significant extent, while the test under controlled potential of the ACF electrode to -0.2 to 1.0 V vs. Ag provides somewhat stable capacitance over 30 cycles.

  19. Influence of salts on the coexistence curve and protein partitioning in nonionic aqueous two-phase micellar systems

    Directory of Open Access Journals (Sweden)

    A. M. Lopes

    2014-12-01

    Full Text Available Aqueous two-phase micellar systems (ATPMS can be exploited in separation science for the extraction/purification of desired biomolecules. Prior to phase separation the surfactant solution reaches a cloud point temperature, which is influenced by the presence of electrolytes. In this work, we provide an investigation on the cloud point behavior of the nonionic surfactant C10E4 in the presence of NaCl, Li2SO4 and KI. We also investigated the salts' influence on a model protein partitioning. NaCl and Li2SO4 promoted a depression of the cloud point. The order of salts and the concentration that decreased the cloud point was: Li2SO4 0.5 M > NaCl 0.5 M ≈ Li2SO4 0.2 M. On the other hand, 0.5 M KI dislocated the curve to higher cloud point values. For our model protein, glucose-6-phosphate dehydrogenase (G6PD, partitioning experiments with 0.5 M NaCl or 0.2 M Li2SO4 at 13.85 ºC showed similar results, with K G6PD ~ 0.46. The lowest partition coefficient was obtained in the presence of 0.5 M KI (K G6PD = 0.12, with major recovery of the enzyme in the micelle-dilute phase (%Recovery = 90%. Our results show that choosing the correct salt to add to ATPMS may be useful to attain the desired partitioning conditions at more extreme temperatures. Furthermore, this system can be effective to separate a target biomolecule from fermented broth contaminants.

  20. Antioxidant activity of aqueous extract of noni in dilutent for ram semen cryopreservation

    Directory of Open Access Journals (Sweden)

    Ana Lauren Costa Nascimento

    2016-03-01

    Full Text Available Noni (Morinda citrifolia L. is a fruit consumed worldwide because of its nutritional and therapeutic properties resulting from the large amount of phenolic compounds, which has aroused interest of the scientific community. In order to identify new natural sources of antioxidants, the objective of this study was to evaluate the performance of noni in diluent for ram semen cryopreservation. A completely randomized design consisting of four treatments and three repetitions per treatment was used. The treatments differed in terms of the concentration of the aqueous extract of noni added to the diluent: control, no addition of the extract, and three concentrations (24, 72, and 120 µg/mL. The physical and chemical variables of the mature fruit were evaluated: total acidity (8.78, pH (4.12, and soluble solids (8.18%. The vitamin C content was 309.42 mg per 100 g fresh matter. The aqueous extract of noni was also evaluated regarding the quantity of total phenolic compounds, antioxidant activity, and lipid peroxidation inhibition capacity. The aqueous extract contained a moderate amount of phenolic compounds (47.96 ± 1.95 mg gallic acid equivalent/100 g extract. The concentrations of the aqueous extract of 72 and 120 µg/mL in diluent used for semen cryopreservation inhibited lipid peroxidation by 21.75% and 51.32%, respectively. There was no positive effect of the lowest concentration (24 µg/mL. The antioxidant activity index of noni was 33.33, corresponding to very strong antioxidant activity. The aqueous extract of noni exhibits very strong antioxidant activity and its addition to the diluent for semen cryopreservation at a concentration of 72 µg/mL is able to inhibit lipid peroxidation.

  1. Solution behaviors and microstructures of PNIPAm-P123-PNIPAm pentablock terpolymers in dilute and concentrated aqueous solutions.

    Science.gov (United States)

    Lu, Yanping; Chen, Tongquan; Mei, Aixiong; Chen, Tianyou; Ding, Yanwei; Zhang, Xinghong; Xu, Junting; Fan, Zhiqiang; Du, Binyang

    2013-06-07

    The solution behaviors and microstructures of poly(N-isopropylacrylamide)x-poly(ethylene oxide)20-poly(propylene oxide)70-poly(ethylene oxide)20-poly(N-isopropylacrylamide)x (PNIPAmx-PEO20-PPO70-PEO20-PNIPAmx or PNIPAmx-P123-PNIPAmx) pentablock terpolymers with various PNIPAm block lengths in dilute and concentrated aqueous solutions were investigated by micro-differential scanning calorimetry (micro-DSC), static and dynamic light scattering (SLS & DLS), and synchrotron small angle X-ray scattering (SAXS). Two lower critical solution temperatures (LCSTs) were observed for PNIPAmx-P123-PNIPAmx pentablock terpolymers in dilute solutions, which corresponded to LCSTs of PPO and PNIPAm blocks, respectively. The LCST of PPO block shifted from 24.4 °C to 29 °C when the length x of PNIPAm block increased from 10 to 97. The LCST of PNIPAm is around 34.5 °C-35.3 °C and less dependent on the block length x. The PNIPAmx-P123-PNIPAmx pentablock terpolymers formed "associate" structures and micelles with hydrophobic PNIPAm and PPO blocks as cores and soluble PEO blocks as coronas in dilute aqueous solutions at 20 °C and 40 °C, respectively, regardless of the relative lengths of PNIPAm, PPO and PEO blocks. The size of "associate" structures of PNIPAmx-P123-PNIPAmx pentablock terpolymers at 20 °C increased with increasing the length of PNIPAm block. The microstructures of PNIPAmx-P123-PNIPAmx hydrogels formed in concentrated aqueous solutions (40 wt%) were strongly dependent on the environmental temperatures and relative lengths of PNIPAm, PPO and PEO blocks as revealed by SAXS. Increasing the length of PNIPAm block weakened the order structures of PNIPAmx-P123-PNIPAmx hydrogels. The microstructures of PNIPAmx-P123-PNIPAmx hydrogels changed from mixed fcc and hex structures for PNIPAm10-P123-PNIPAm10 to isotropic structure for PNIPAm97-P123-PNIPAm97. Increasing temperature led to the transition from mixed hex and fcc structure to pure hex structure for PNIPAm10-P123-PNIPAm

  2. The cluster structure of dilute aqueous-alcoholic solutions and molecular light scattering in them

    Science.gov (United States)

    Malomuzh, N. P.; Slinchak, E. L.

    2007-11-01

    The structures, equations of state, and character of fluctuations of dilute water-glycerol solutions are discussed. Two or three glycerol and about ten water molecules were found to form a fairly stable molecular complex. We call this complex elementary cluster (pseudoparticle). In a certain region of state parameters, the system could be considered a solution of pseudoparticles (clusters). Its properties were modeled by the van der Waals equation. The character of interactions between clusters was analyzed. An anomalous increase in concentration and molecular light scattering fluctuations was caused by the approach to the solution “pseudospinodal.” The experimental data were found to be in quite satisfactory agreement with theoretical estimates.

  3. Removal of β—Naphthalenesulfonic Acid from Aqueous Dilute Solution Using Bagasse Fly Ash

    Institute of Scientific and Technical Information of China (English)

    LIChanghai; SHIPengfei

    2002-01-01

    Bagasse fly ash was converted into an inexpensive adsorbent and utilized for the removal of β-naphthalenesulfonic acid in dilute solution.The effect of pH,temperature,adsorbent concentration,and co-existed acids on the removal of β-naphthalenesulfonic acid was examined. The adsorption data have been correlated with both Lagnmuir and Freundlich adsorption models.Thermodynamic parameters obtained indicate the feasibility of the process,and kinetic studies provided the necessary mechanistic information of the removal process.

  4. Prediction of infinite dilution activity coefficients of chlorinated organic compounds in aqueous solution from quantum-chemical descriptors.

    Science.gov (United States)

    Delgado, Eduardo J.; Alderete, Joel B.

    2001-11-30

    A quantitative structure-property relationship (QSPR) model is developed to correlate the natural logarithm of infinite dilution activity coefficients, ln (gamma(infinity)), of 45 chlorinated organic compounds in aqueous solution from quantum-chemical descriptors. The best correlation equation contains five theoretical molecular descriptors. All descriptors were obtained from the chemical structure of the compounds and have definite physical meaning corresponding to different intermolecular interactions. The model predicts ln (gamma(infinity)) with a correlation coefficients of 0.949 and a standard error of 0.442 ln units. The obtained QSPR equation may be applied to the prediction of gamma(infinity) of other chlorinated organic compounds not present in the data set used for the development of the present model. Copyright 2001 John Wiley & Sons, Inc. J Comput Chem 22: 1851-1856, 2001

  5. Microcapsules containing ionic liquid [A336][P507] for La3+/Sm3+/Er3+recovery from dilute aqueous solution

    Institute of Scientific and Technical Information of China (English)

    王月; 王运东; 靖宇; 陈继; 刘郁

    2016-01-01

    The efficacy of polysulfone microcapsules encapsulating ionic liquid [trialkylmethylammonium][di(2-ethylhelxyl) ortho-phosphinate] ([A336][P507]) for the extraction of La3+, Sm3+ and Er3+ from dilute aqueous solutions was investigated. Microcapsules were synthesized using coaxial microfluidic method, and subsequently encapsulated with extractant [A336][P507]. The kinetics data were fitted well by pseudo-second-order equation and Crank model, and the kinetics parameters were evaluated. The extraction rate had the order of Er3+>Sm3+>La3+. The isotherm data were analyzed by Langmuir model and shifted Langmuir model. The extraction capacities of La3+, Sm3+ and Er3+ were 58.4, 56.6 and 81.7 mg/g, respectively. The dependency of stripping performance on HNO3 concentration was measured. The regeneration of microcapsules was evaluated using cycling extraction experiments.

  6. Theoretical study of the Pb(II)-catechol system in dilute aqueous solution: Complex structure and metal coordination sphere determination

    Science.gov (United States)

    Lapouge, Christine; Cornard, Jean-Paul

    2010-04-01

    We investigated the unknown interaction of Pb(II) with catechol ligand in diluted aqueous solution by electronic spectroscopies combined with quantum chemical calculations. The aim of this work is the determination of the complete structure of the complex formed and particularly the metal coordination sphere. Three successive steps have been necessary to reach this goal: (i) the comparison of the experimental electronic absorption spectrum with theoretical spectra calculated from various hypothetical structures, (ii) complexation reaction pathways calculations in vacuum and with taking into account the solvent effects and finally (iii) the fluorescence emission wavelength calculations. All these investigations led to identify a monodentate complex with the monodeprotonated ligand, in which the Pb atom presents a coordination number of five. The formula of the complex is [Pb(Hcat)(HO)4]mono+.

  7. Self-organization of poly(ethylene oxide) on the surface of aqueous salt solutions.

    Science.gov (United States)

    Fuchs, Christian; Hussain, Hazrat; Amado, Elkin; Busse, Karsten; Kressler, Joerg

    2015-01-01

    It is demonstrated that stable Langmuir films of poly(ethylene oxide) (PEO) can be formed up to surface pressures of 30 mN m(-1) when potassium carbonate K2CO3 is added to the aqueous subphase. Generally, PEO homopolymer cannot stay on the water surface at a surface pressure ≥10 mN m(-1) due to its high water solubility. To prepare stable monolayer films, PEO can be modified with hydrophobic moieties. However, by exploiting the salting out effect by adding certain salts (K2CO3 or MgSO4) into the aqueous subphase, not only very stable films but also unusual self-organization can be achieved by the PEO homopolymer on the surface of the aqueous solution. Thus, a series of OH-terminated PEOs is found to form a stable monolayer at K2CO3 concentrations of 2 M and above in the aqueous subphase, and the stability of the film increases with an increase in K2CO3 concentration. Hysteresis experiments are also carried out. During the phase transition induced by progressive compression, self-organization into well-defined domains with sizes in the micrometer range are observed, and with further compression and holding of the film for 30 min and above the microdomains transform into a crystalline morphology as visualized by Brewster angle microscopy. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. Characterizing Soy Sauce Moromi Manufactured by High-Salt Dilute-State and Low-Salt Solid-State Fermentation Using Multiphase Analyzing Methods.

    Science.gov (United States)

    Zhang, Liqiang; Zhou, Rongqing; Cui, Ruiying; Huang, Jun; Wu, Chongde

    2016-10-14

    Present study was to characterize the physiochemical properties, free amino acids (FAAs), volatiles and microbial communities of various moromi, respectively sampled from different stages of high-salt dilute-state (HSDS) and low-salt solid-state (LSSS) fermentation, using multiphase analyzing methods. Phospholipid fatty acids (PLFA) analysis indicated that Gram-positive bacteria were dominant bacteria and fungi were principal microbes. For DGGE analysis, dominant microbes in moromi were mainly fell into Weissella, Tetragenococcus, Candida, Pichia, and Zygosaccharomyces. During fermentation, the dominant microbes shifted from nonhalophilic and less acid-tolerant species to halophilic and acid-tolerant species. Total of 15 FAAs and 44 volatiles were identified in moromi, mainly Glu, Asp, Tyr, and acids, alcohols, esters, aldehydes, respectively. Odor activity values analysis suggested that the final moromi of LSSS fermentation had more complicated odors than that of HSDS fermentation. Conclusively, technological parameters, microbial communities, raw materials and fermentation process may result in the discrepancy of HSDS and LSSS moromi.

  9. Dielectric analysis on phase transition and micelle shape of polyoxyethylene trisiloxane surfactant in dilute aqueous solution

    Institute of Scientific and Technical Information of China (English)

    Ya Wen Zhou; Wei Zhou; Fu Han; Bao Cai Xu

    2011-01-01

    The cloudy Silwet L-77 aqueous solution on the concentration range from 0.5% to 50% was investigated by dielectric relaxation spectroscopy. The concentration dependence of phase microstructure was confirmed by means of analyzing the dielectric parameters of bulk solution. The relaxation behavior was assigned to the interfacial polarization between the micelle and the medium, and the relaxation distribution parameter was used to figure the shape transition from sphere to ellipsoid with the concentration increasing. The synchronous reduction of permittivity and conductivity indicated the formation of the lamellar phase. As compensation, the quantity of the surfactant liquid phase gradually decreased, whose shape constantly kept ellipsoidal.

  10. "Structure-making" ability of Na+ in dilute aqueous solution: an ONIOM-XS MD simulation study.

    Science.gov (United States)

    Sripa, Pattrawan; Tongraar, Anan; Kerdcharoen, Teerakiat

    2013-02-28

    An ONIOM-XS MD simulation has been performed to characterize the "structure-making" ability of Na(+) in dilute aqueous solution. The region of most interest, i.e., a sphere that includes Na(+) and its surrounding water molecules, was treated at the HF level of accuracy using LANL2DZ and DZP basis sets for the ion and waters, respectively, whereas the rest of the system was described by classical pair potentials. Detailed analyzes of the ONIOM-XS MD trajectories clearly show that Na(+) is able to order the structure of waters in its surroundings, forming two prevalent Na(+)(H(2)O)(5) and Na(+)(H(2)O)(6) species. Interestingly, it is observed that these 5-fold and 6-fold coordinated complexes can convert back and forth with some degrees of flexibility, leading to frequent rearrangements of the Na(+) hydrates as well as numerous attempts of inner-shell water molecules to interchange with waters in the outer region. Such a phenomenon clearly demonstrates the weak "structure-making" ability of Na(+) in aqueous solution.

  11. The effect of temperature on radiolysis of iodide ion diluted aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Gorbovitskaya, T.; Tiliks, J. [Latvia Univ., Lab. of Radiation Chemistry, Riga (Latvia)

    1996-12-01

    To investigate the radiolysis of iodine containing aqueous solutions a flow type facility (ITF) has a possibility to irradiate aqueous solutions in the steel vessel with {sup 60}Co {gamma}-rays and continuously (on line) to analyze the products of radiolysis both in liquid and in gaseous phases. By means of ITF the formation of I{sub ox} (I{sub 2} + I{sub 3}{sup -} + HOI), IO{sub 3}{sup -}, H{sub 2}O{sub 2} was studied in 10{sup -5} - 10{sup -3} mol/dm{sup 3} CsI aqueous solutions by their radiolysis at dose rate 4.5 kGv/h for six hours in region of temperatures from 313 to 404 K. Some experiments in glass ampoules were also performed. The steady-state concentrations of I{sub ox} and IO{sub 3}{sup -} decreased with increasing temperature as linear function of inverted temperature. The effect decreased with decreasing concentration of iodide ion. As the result, at high temperatures (T{>=}380 K) the steady-state concentration of I{sub ox} does not depend essentially on the iodide ion initial concentration. Molecular iodine (I{sub 2}) released from the solution was the main radiolysis product in gaseous phase. Its steady-state concentration increased with increasing temperature because of iodine solubility in the water and decreased at the same time because the radiolytic iodine concentrations decreased. Therefore the most volatility of irradiated 10{sup -3} and 10{sup -4}M CsI solutions was observed at the temperature about 350 K. The volatility of 10{sup -5}M solutions gradually decreased with increasing temperature. The experimental data were explained on the base of the hypothesis that the reaction between I{sub 2} and radiolytic H{sub 2}O{sub 2} was the limit one determining the temperature dependence of I{sub ox} and IO{sub 3}{sup -}steady-state concentrations. Its activation energy was estimated to be 27,5 kcal.mol{sup -1}. The temperature dependence for reaction (IO{sup -} + H{sub 2}O{sub 2}) was also estimated. (author) 8 figs., 1 tab., 17 refs.

  12. Lyotropic, liquid crystalline nanostructures of aqueous dilutions of SMEDDS revealed by small-angle X-ray scattering: impact on solubility and drug release.

    Science.gov (United States)

    Goddeeris, Caroline; Goderis, Bart; Van den Mooter, Guy

    2010-05-12

    The present study was conducted to characterise the liquid crystalline phases that occur upon diluting a SMEDDS and to elucidate the role of these phases on drug solubilisation and release. Small-angle X-ray scattering (SAXS) was used to probe the structures in aqueous dilutions of 3 SMEDDS consisting of propylene glycol mono- and dicaprylate and mono- and dicaprate (PGDCDC) and d-alpha-tocopheryl polyethylene glycol succinate 1000 (TPGS 1000), polysorbate 80 (P80) or polyoxyl 40 hydrogenated castor oil (P40HC). The scattering patterns revealed the formation of either a random periodic or a lamellar phase when 10% (w/w) water was added. All formulations exhibited lamellar structures at 20% (w/w) aqueous dilution, of which the layer-to-layer distance increased upon further addition of water. At 40% (w/w) water, a hexagonal or lamellar phase was formed, depending on the geometry of the surfactant. Temperature did not alter the phases formed. Incorporation of the drug UC 781 only slightly enlarged the characteristic dimensions of the liquid crystalline phases. Drug solubility decreased upon aqueous dilution, although 10% (w/w) dilutions of PGDCDC-P80 SMEDDS and PGDCDC-TPGS 1000 SMEDDS revealed a highly increased solubility as compared to the pure formulations. Drug release data revealed that UC 781 release could not be linked to the solubilisation capacity of the SMEDDS, but could be associated with the solubility of UC 781 in the phases formed at water concentrations above 10% (w/w).

  13. Cu(II)effect on the conformation of regenerated silk fibroin in dilute aqueous solution

    Institute of Scientific and Technical Information of China (English)

    ZONG Xiaohong; ZHOU Ping; SHAO Zhengzhong; WANG Honghai; CHUNYU Lijuan

    2005-01-01

    Much attention has been paid to the natural mechanism of silkworm spinning due to the impressive mechanical properties of the natural fibers. In this work, we studied the effect of Cu(II) ions on the secondary structure of Bombyx mori regenerated silk fibroin (SF) in dilute solution by circular dichroism (CD). The results indicate that a given amount of Cu(II) induces the SF conformational transition from random coil to β-sheet, however, further addition of Cu(II) is unfavorable for this conversion. Meanwhile, the conformational changes induced by Cu(II) follow a nucleation-dependent aggregation mechanism, which is similar to that found in Prion protein (PrP) denaturation and Aβ-pep- tide aggregations, leading to the neurodegenerative disease. This work would help one understand further the natural spinning process of silkworm. Additionally, it would be significant for the study of the nervous system diseases, because silk fibroin, extracted in large amounts from Bombyx mori silkworm gland, could be a proper model to study PrP denaturation and Aβ-peptide aggregations.

  14. Bridged heterocyclium dicationic closo-icosahedral perfluoroborane, borane, and carborane salts via aqueous, open-air benchtop synthesis.

    Science.gov (United States)

    Shackelford, Scott A; Belletire, John L; Boatz, Jerry A; Schneider, Stefan; Wheaton, Amanda K; Wight, Brett A; Ammon, Herman L; Peryshkov, Dmitry V; Strauss, Steven H

    2010-06-18

    Thirteen bridged triazolium and imidazolium dicationic salts, which uniquely pair closo-icosahedral perfluoroborane [B(12)F(12)](2-), borane [B(12)H(12)](2-), or carborane [CB(11)H(12)](-) anionic species with unsaturated bridged heterocyclium dications, were synthesized using an aqueous benchtop method. This considerably extends the scope of a reported aqueous synthesis of binary [heterocyclium](2)[B(12)H(12)] and [heterocyclium][CB(11)H(12)] salts. Also, the one-step preparation of five new precursor bridged heterocyclium dicationic dihalide salts using conventional procedures and in one case a microwave-assisted method is described.

  15. Separation of compounds with multiple -OH groups from dilute aqueous solutions via complexation with organoboronate

    Energy Technology Data Exchange (ETDEWEB)

    Chow, Tina Kuo Fung

    1992-05-01

    The complexing extractant agent investigated in this work is 3-nitrophenylboronic acid (NPBA) in its anionic form (NPB). NPBA and Aliquat 336 (quaternary amine) is dissolved in 2-ethyl-l-hexanol, and the extractant is contacted with aq. NaOH. Solutes investigated were 1,2-propanediol, glycerol, fructose, sorbitol and lactic acid. Batch extraction experiments were performed at 25{degree}C. Partition coefficients, distribution ratios and loadings are reported for varying concentrations of solute and NPB. All solutes complexed with NPB{sup {minus}}, with all complexes containing only one NPB{sup {minus}} per complex. The 1:1 complexation constants for the solutes glycerol, fructose and sorbitol follow trends similar to complexation with B(OH){sub 4}{sup {minus}} (aq.), i.e. the complexation constants increase with increasing number of {minus}OH groups available for complexation. Assumption of 1:1 complex is not valid for 1, 2-propanediol, which showed overloading (more than one mole of solute complexed to one mole NPB{sup {minus}}) at higher concentrations. The {minus}OH group on the NPB{sup {minus}} which is left uncomplexed after one solute molecule had bound to the other two {minus}OH groups may be responsible for the overloading. Overloading is also observed in extraction of tactic acid, but through a different mechanism. It was found that TOMA{sup +} can extract lactic acid to an extent comparable to the uptake of lactic acid by NPB{sup {minus}}. The complexation is probably through formation of an acid-base ion pair. Losses of NPBA into the aqueous phase could lead to problems, poor economics in industrial separation processes. One way of overcoming this problem would be to incorporate the NPBA onto a solid support.

  16. Aqueous geochemistry on Mars: Possible clues from salts and clays in SNC meteorites

    Science.gov (United States)

    Gooding, James L.

    1992-01-01

    All subgroups of the shergottite, nakhlite, and chassignite (SNC) meteorites contain traces of water precipitated minerals that include various combinations of carbonates, sulfates, halides, ferric oxides, and aluminosilicate clays of preterrestrial origin. Oxygen three-isotope analysis of thermally extracted bulk water has confirmed that at least some of the water in SNC's is, indeed, extraterrestrial. A mixture of aqueous precipitates found in the SNC's, comprising smectite, illite, and gypsum (with minor halite +/- calcite and hematite), provides a self-consistent, though not unique, model for the bulk elemental composition of surface sediments at the Viking Lander sites. Therefore, if the salts and clays in SNC's are truly linked to aqueous alteration and soil formation on Mars, then the suite of SNC secondary minerals might provide the best currently available insight into near-surface martian chemistry.

  17. Characterization of reaction products of iron and iron salts and aqueous plant extracts

    Energy Technology Data Exchange (ETDEWEB)

    Jaen, J.A. [Universidad de Panama, Centro de Investigaciones con Tecnicas Nucleares/Depto. de Quimica (Panama); Garcia de Saldana, E.; Hernandez, C. [Universidad de Panama, Maestria en Ciencias Quimicas (Panama)

    1999-11-15

    The complexes formed in aqueous solution as a result of a reaction of iron and iron salts (Fe{sup 2+} and Fe{sup 3+}) and some plant extracts were analyzed using Moessbauer spectroscopy and Fourier transform infrared. The extracts were obtained from Opuntia elatior mill., Acanthocereus pentagonus (L.) Britton, Mimosa tenuiflora, Caesalpinia coriaria (Jacq.) Willd., Bumbacopsis quinata (Jacq.) Dugand and Acacia mangium Willd., plants growing wildly in different zones of the Isthmus of Panama. Results suggest the formation of mono- and bis-type complexes, and in some cases, the occurrence of a redox reaction. The feasibility of application of the studied extracts as atmospheric corrosion inhibitors is discussed.

  18. Characterization of reaction products of iron and iron salts and aqueous plant extracts

    Science.gov (United States)

    Jaén, J. A.; García de Saldaña, E.; Hernández, C.

    1999-11-01

    The complexes formed in aqueous solution as a result of a reaction of iron and iron salts (Fe2+ and Fe3+) and some plant extracts were analyzed using Mössbauer spectroscopy and Fourier transform infrared. The extracts were obtained from Opuntia elatior mill., Acanthocereus pentagonus (L.) Britton, Mimosa tenuiflora, Caesalpinia coriaria (Jacq.) Willd., Bumbacopsis quinata (Jacq.) Dugand and Acacia mangium Willd., plants growing wildly in different zones of the Isthmus of Panama. Results suggest the formation of mono- and bis-type complexes, and in some cases, the occurrence of a redox reaction. The feasibility of application of the studied extracts as atmospheric corrosion inhibitors is discussed.

  19. Salting-Out of Methane in the Aqueous Solutions of Urea and Glycine-Betaine.

    Science.gov (United States)

    Dixit, Mayank Kumar; Siddique, Asrar A; Tembe, B L

    2015-08-27

    We have studied the hydrophobic association and solvation of methane molecules in aqueous solutions of urea and glycine betaine (GB). We have calculated the potentials of mean force (PMFs) between methane molecules in water, aqueous GB, aqueous urea and aqueous urea-GB mixtures. The PMFs and equilibrium constants indicate that both urea and GB increase the hydrophobic association of methane. Calculation of thermodynamic parameters shows that the association of methane is stabilized by entropy whereas solvation is favored by enthalpy. In the case of the water-urea-GB mixture, both hydrophobic association and solvation are stabilized by entropy. From the investigation of radial distribution functions, running coordination numbers and excess coordination numbers, we infer that both urea and GB are preferentially excluded from methane surface in the mixtures of osmolytes and methane is preferentially solvated by water molecules in all the mixtures. The favorable exclusion of both urea and GB from the methane surface suggests that both urea and GB increase the interaction between methane molecules, i.e., salting-out of methane. We observe that addition of both urea and GB to water enhances local water structure. The calculated values of diffusion constants of water also suggest enhanced water-water interactions in the presence of urea and GB. The calculated free energies of methane in these mixtures show that methane is less soluble in the mixtures of urea and GB than in water. The data on solvation free energies support the observations obtained from the PMFs of methane molecules.

  20. Study of quantitative interactions of potato and corn starch granules with ions in diluted solutions of heavy metal salts.

    Science.gov (United States)

    Szymońska, Joanna; Molenda, Marcin; Wieczorek, Jerzy

    2015-12-10

    Interactions of potato and corn starch granules with ions in diluted solutions of silver, lead, copper or iron salts were investigated. It was shown experimentally that granules accumulated the cations in amounts depending on the granule structure and water content as well as a type of both metal and counter-ions present in solution. Potato starch retained almost three times more cations compared to corn starch what was proportional to the total phosphorous content in these starches. Quantity of milligrams of cations bound by 1g of starch was inversely correlated with the cation hydration. Ag(+), Pb(2+) and Cu(2+) were connected in stoichiometric amounts of moles to semicrystalline and amorphous parts of the granules. Fe(3+) ions were accumulated in higher than stoichiometric quantities mainly in granule amorphous regions. Metal ions penetrated into granules together with anions except nitrates which remained on surface of potato starch granules. Cations facilitated the starch thermal decomposition in accordance with values of their standard redox potentials. Nitrates supported this process only in the presence of base metal cations.

  1. Efficient adsorption of both methyl orange and chromium from their aqueous mixtures using a quaternary ammonium salt modified chitosan magnetic composite adsorbent.

    Science.gov (United States)

    Li, Kun; Li, Pei; Cai, Jun; Xiao, Shoujun; Yang, Hu; Li, Aimin

    2016-07-01

    A quaternary ammonium salt modified chitosan magnetic composite adsorbent (CS-CTA-MCM) was prepared by combination of Fe3O4 nanoparticles. Various techniques were used to characterize the molecular structure, surface morphology, and magnetic feature of this composite adsorbent. CS-CTA-MCM was employed for the removal of Cr(VI) and methyl orange (MO), an anionic dye, from water in respective single and binary systems. Compared with chitosan magnetic adsorbent (CS-MCM) without modification, CS-CTA-MCM shows evidently improved adsorption capacities for both pollutants ascribed to the additional quaternary ammonium salt groups. Based on the adsorption equilibrium study, MO bears more affinity to CS-CTA-MCM than Cr(VI) causing a considerable extent of preferential adsorption of dye over metal ions in their aqueous mixture. However, at weak acidic solutions, Cr(VI) adsorption is evidently improved due to more efficient Cr(VI) forms, i.e. dichromate and monovalent chromate, binding to this chitosan-based adsorbent. Thus chromium could be efficient removal together with MO at suitable pH conditions. The adsorption isotherms and kinetics indicate that adsorptions of Cr(VI) and MO by CS-CTA-MCM both follow a homogeneous monolayer chemisorption process. This magnetic adsorbent after saturated adsorption could be rapidly separated from water and easily regenerated using dilute NaOH aqueous solutions then virtually reused with little adsorption capacity loss.

  2. Adsorption of small biological molecules on silica from diluted aqueous solutions: Quantitative characterization and implications to the Bernal's hypothesis

    Science.gov (United States)

    Basiuk, Vladimir A.; Gromovoy, Taras Yu.; Khil'Chevskaya, Elena G.

    1995-08-01

    To describe quantitatively the adsorption of prebiotically important compounds of low molecular weight (amino acids, short linear peptides, cyclic dipeptides, the Krebs's cycle and other carboxylic acids, nucleosides and related phosphates) on silica surface from diluted neutral aqueous solutions, equilibrium constants (K) and free energies (-ΔG) of adsorption were determined from the retention values measured by means of high-performance liquid chromatography on a silica gel column and from the isotherms measured under static conditions. For most carboxylic acids (including amino acids and linear peptides) -ΔG values were negative and K0 and K>1 were found for most of them. Influence of the structure of α-substituent on the adsorbability is analyzed. A linear dependence of -ΔG on the number of aliphatic carbon atoms in a sorbate molecule was found for the series of aliphatic bifunctional amino acids, related dipeptides and 2,5-piperazinediones, as well as for the row from glycine to triglycyl glycine. The adsorption of nucleosides and their phosphates is characterized by much higherK and -ΔG values (of the order of 102 and 104, respectively). The adsorption data available from our work and literature are summarized and discussed with implications to the Bernal's hypothesis on the roles of solid surfaces in the prebiotic formation of biopolymers from monomeric ‘building blocks’.

  3. Tritium Separation from High Volume Dilute Aqueous Streams- Milestone Report for M3FT-15OR0302092

    Energy Technology Data Exchange (ETDEWEB)

    Bhave, Ramesh R. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jubin, Robert Thomas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Spencer, Barry B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Nair, S. [Georgia Inst. of Technology, Atlanta, GA (United States)

    2016-02-29

    This report describes the synthesis and evaluation of molecular sieve zeolite membranes to separate and concentrate tritiated water (HTO) from dilute HTO-bearing aqueous streams. Several silico alumino phosphate (SAPO-34) molecular sieve zeolite membranes were synthesized and characterized with gas and vapor permeation measurements. The pervaporation process performance was evaluated for the separation and concentration of tritiated water. Experiments were performed over a range of tritiated water concentration covering the range of concentration anticipated in nuclear fuel processing where potentially both acid and water streams are recycled. The permeate was recovered under vacuum. The tritium concentration ranged from 0.5 to 1 mCi/mL which is about 0.1 mg/L or 0.1 ppm. The HTO concentration was three orders of magnitude lower than experiments performed with simulated feed containing HDO (>100 ppm) using deuterated water where high separation factors (>10) were obtained using SAPO membranes. Separation factor calculated from the measured tritium concentrations ranged from 0.83-0.98. Although the membrane performance characterization results were lower than expected, they can be explained on the basis of low feed volume and three orders of magnitude lower HTO concentration compared to HDO concentration in deuterated water. We have identified several new approaches, such as tuning the diffusion coefficient of HTO, that may help achieve preferential transport of tritium (HTO) resulting in a substantially more concentrated permeate.

  4. Coarse-grained model of glycosaminoglycans in aqueous salt solutions. A field-theoretical approach.

    Science.gov (United States)

    Kolesnikov, Andrei L; Budkov, Yurij A; Nogovitsyn, Evgenij A

    2014-11-20

    We present results of self-consistent field calculations of thermodynamic and structural properties of glycosaminoglycans (chondroitin sulfate, hyaluronic acid, and heparin) in aqueous solutions with added monovalent and divalent salts. A semiphenomenological coarse-grained model for semiflexible polyelectrolyte chains in solution is proposed. The coarse-grained model permits one to focus on the essential features of these systems and provides significant computational advantages with respect to more detailed models. Our approach relies on the method of Gaussian equivalent representation for the calculation of the partition functions in the form of functional integrals. This method provides reliable thermodynamic information for polyelectrolyte solutions over wide ranges of monomer concentrations. In the present work, we use the comparison and fitting of the experimental osmotic pressure with a theoretical equation of state within the Gaussian equivalent representation. The degrees of ionization, radii of gyration, persistence lengths, and structure factors of chondroitin sulfate, hyaluronic acid, and heparin in aqueous solutions with added monovalent and divalent salts are calculated and discussed.

  5. Synthesis of fast response crosslinked PVA-g-NIPAAm nanohydrogels by very low radiation dose in dilute aqueous solution

    Science.gov (United States)

    Fathi, Marziyeh; Reza Farajollahi, Ali; Akbar Entezami, Ali

    2013-05-01

    Nanohydrogels of poly(vinyl alcohol)-g-N-isopropylacrylamide (PVA-g-NIPAAm) are synthesized by PVA and NIPAAm dilute aqueous solution using much less radiation dose of 1-20 Gy via intramolecular crosslinking at ambient temperature. The radiation synthesis of nanohydrogels is performed in the presence of tetrakis (hydroxymethyl) phosphonium chloride (THPC) due to its rapid oxygen scavenging abilities and hydrogen peroxide (H2O2) as a source of hydroxyl radicals. The effect of radiation dose, feed composition ratio of PVA and H2O2 is investigated on swelling properties such as temperature and pH dependence of equilibrium swelling ratio as well as deswelling kinetics. Experimental data exhibit high equilibrium swelling ratio and fast response time for the synthesized nanohydrogels. The average molecular weight between crosslinks (Mc) and crosslinking density (ρx) of the obtained nanohydrogels are calculated from swelling data as a function of radiation dose, H2O2 and PVA amount. Fourier transform infrared spectroscopy (FT-IR), elemental analysis of nitrogen content and thermogravimetric analysis (TGA) are used to confirm the grafting reaction. Lower critical solution temperature (LCST) is measured around 33 °C by differential scanning calorimetry (DSC) for PVA-g-NIPAAm nanohydrogels. Dynamic light scattering (DLS) data demonstrate that the increase of radiation dose leads to the decreasing in dimension of nanohydrogels. Also, rheological studies are confirmed an improvement in the mechanical properties of the nanohydrogels with increasing the radiation dose. A cytotoxicity study exhibits a good biocompatibility for the obtained nanohydrogels. The prepared nanohydrogels show fast swelling/deswelling behavior, high swelling ratio, dual sensitivity and good cytocompatibility, which may find potential applications as biomaterial.

  6. Thermodynamic modelling of phase equilibrium for water + poly(Ethylene glycol + salt aqueous two-phase systems

    Directory of Open Access Journals (Sweden)

    R.A.G. Sé

    2002-04-01

    Full Text Available The NRTL (nonrandom, two-liquid model, expressed in mass fraction instead of mole fraction, was used to correlate liquid-liquid equilibria for aqueous two-phase polymer-salt solutions. New interaction energy parameters for this model were determined using reported data on the water + poly(ethylene glycol + salt systems, with different molecular masses for PEG and the salts potassium phosphate, sodium sulfate, sodium carbonate and magnesium sulfate. The correlation of liquid-liquid equilibrium is quite satisfactory.

  7. Scale-up of osmotic membrane bioreactors by modeling salt accumulation and draw solution dilution using hollow-fiber membrane characteristics and operation conditions.

    Science.gov (United States)

    Kim, Suhan

    2014-08-01

    A full-scale osmotic membrane bioreactor (OMBR) model was developed to simulate salt accumulation, draw solution (DS) dilution, and water flux over the hollow-fiber membrane length. The model uses the OMBR design parameters, DS properties, and forward osmosis (FO) membrane characteristics obtained from lab-scale tests. The modeling results revealed a tremendous water flux decline (10→0.82LMH) and short solids retention time (SRT: 5days) due to salt accumulation and DS dilution when OMBR is scaled up using commercially available DS and FO membrane. Simulated water flux is a result of interplay among reverse salt flux, internal and external concentration polarization (ICP and ECP). ECP adversely impacts water flux considerably in full-scale OMBR although it is often ignored in previous works. The OMBR model makes it possible to select better DS properties (higher flow rate and salt concentration) and FO membranes with higher water flux propensity in full-scale operation. Copyright © 2014 Elsevier Ltd. All rights reserved.

  8. Characteristics and quantitative of negative ion in salt aqueous solution by Raman spectroscopy at -170℃

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The results from Raman spectroscopy analysis of salt aqueous solutions at -170℃ demonstrate that for those clearly sharp iron peaks whose Raman wavenumber is close to each other such as and , their original shape could be restorable by the stripping technique, and that ice's sharp characteristic peak (3090-3109 cm-1) is steady, while the spectrum band of the complex compound (nCl--[H+-OH-]n) chlorine ion combined chemically with water molecule is 3401-3413 cm-1. On the other hand, the research shows that the higher the negative iron concentration, the stronger its Raman characteristic peak intensity and the smaller the ice's. Based on the number of data and theoretical work, the strong correlation of the molar concentration of negative ion with the band area ratio is built up. Moreover, the developed Raman method is successfully used in the component analysis of the field fluid inclusions from Silurian sandstone in Tarim basin.

  9. Rheological properties and thickening mechanism of aqueous diutan gum solution: Effects of temperature and salts.

    Science.gov (United States)

    Xu, Long; Gong, Houjian; Dong, Mingzhe; Li, Yajun

    2015-11-05

    Rheological properties of a new microbial polysaccharide, diutan gum in aqueous solution have been systematically investigated. It is found that molecular aggregates of diutan gum can be formed at a very low concentration (0.12 g/L), and the mechanism of thickening by diutan gum is proposed. The viscosity retention rate of diutan gum changes little when increasing the temperature from 298 K to 348 K or in a high salinity solution (55.5 g L(-1)). Gel structure can be formed in the diutan gum solution, owing to the finding that the dynamic modulus has an exponential relationship with the concentration. The gel properties of diutan gum are not sensitive to temperature, and are virtually independent of cationic environment (Na(+) and Ca(2+)). The temperature/salt tolerance of the diutan gum solution is mainly attributed to its perfect double helix molecular conformation, the location of the side chains of its molecules, and its water retention capacity.

  10. A new method for preparation of magnetite from iron oxyhydroxide or iron oxide and ferrous salt in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Kahani, S.A. [Department of Chemistry, Faculty of Science, University of Kashan, Kashan 87317-51167 (Iran, Islamic Republic of)], E-mail: Kahani@kashanu.ac.ir; Jafari, M. [Department of Chemistry, Faculty of Science, University of Kashan, Kashan 87317-51167 (Iran, Islamic Republic of)

    2009-07-15

    In this study, a new method is proposed for the preparation of Fe{sub 3}O{sub 4} from iron oxyhydroxides (goethite, akaganeite, lepidocrocite, feroxyhyte and ferrihydrite) or iron oxide (hematite) and ferrous salt in aqueous solution. The product is magnetite with various particle sizes. Products are characterized by X-ray powder diffraction, IR spectra and vibrating sample magnetometery.

  11. Chemical equilibrium of hydrogen and aqueous solutions of 1 : 1 bicarbonate and formate salts with a common cation

    NARCIS (Netherlands)

    Engel, D.C.; Versteeg, G.F.; Swaaij, W.P.M. van

    1997-01-01

    The chemical equilibrium of hydrogen and aqueous solutions of 1:1 bicarbonate and formate salts with a common cation has been investigated in an intensively stirred batch reactor: MHCO3(aq) + H2(aq) ↔ MOOCH(aq) + H2O(l) This was accomplished for the sodium (M = Na), potassium (M = K) and ammonium (M

  12. Chemical equilibrium of hydrogen and aqueous solutions of 1 : 1 bicarbonate and formate salts with a common cation

    NARCIS (Netherlands)

    Engel, D.C.; Versteeg, G.F.; Swaaij, W.P.M. van

    1997-01-01

    The chemical equilibrium of hydrogen and aqueous solutions of 1:1 bicarbonate and formate salts with a common cation has been investigated in an intensively stirred batch reactor: MHCO3(aq) + H2(aq) ↔ MOOCH(aq) + H2O(l) This was accomplished for the sodium (M = Na), potassium (M = K) and ammonium (M

  13. Improving the aqueous solubility of triclosan by solubilization, complexation, and in situ salt formation.

    Science.gov (United States)

    Grove, Christine; Liebenberg, Wilna; du Preez, Jan L; Yang, Wenzhan; de Villiers, Melgardt M

    2003-01-01

    Triclosan, an antimicrobial, although widely incorporated into many skin care products, toothpastes, and liquid soaps, presents formulation difficulties because it is practically insoluble in water. The objective of this study was to improve the aqueous solubility of triclosan through solubilization, complexation, and salt formation. The solubility of triclosan in distilled water and in phosphate buffers (pH 7.4) was determined at 30 degrees C. The order of solubilizing performance of the solubilizers was: N-methylglucamine> or =L-arginine>sodium lauryl sulfate>beta-cyclodextrin> or =hydroxypropyl-beta-cyclodextrin>ethanolamine>sodium benzoate>sodium methyl 4-hydroxybenzoate>triethanolamine> or =diethanolamine. These solubilizers increased the solubility of triclosan from 80- to 6000-fold. Micellar solubilization and the formation of either salts or complexes are postulated as possible mechanisms for the increase in the solubility of triclosan by the surfactant sodium lauryl sulphate, the cyclic sugar derivatives beta-cyclodextrin and 2-hydropropyl-beta-cyclodextrin, the amino acid L-arginine, and the amino sugar alcohol N-methylglucamine. Furthermore, although the bacteriostatic efficacy of triclosan was significantly increased when solubilized with N-methylglucamine, L-arginine, and ethanolamine, increased solubilization did not increase the effectiveness of triclosan for all solubilizers tested.

  14. Direct Aqueous Mineral Carbonation of Waste Slate Using Ammonium Salt Solutions

    Directory of Open Access Journals (Sweden)

    Hwanju Jo

    2015-12-01

    Full Text Available The carbonation of asbestos-containing waste slate using a direct aqueous mineral carbonation method was evaluated. Leaching and carbonation tests were conducted on asbestos-containing waste slate using ammonium salt (CH3COONH4, NH4NO3, and NH4HSO4 solutions at various concentrations. The CH3COONH4 solution had the highest Ca-leaching efficiency (17%–35% and the NH4HSO4 solution had the highest Mg-leaching efficiency (7%–24% at various solid dosages and solvent concentrations. The CaCO3 content of the reacted materials based on thermogravimetric analysis (TGA was approximately 10%–17% higher than that of the as-received material for the 1 M CH3COONH4 and the 1 M NH4HSO4 solutions. The carbonates were precipitated on the surface of chrysotile, which was contained in the waste slate reacted with CO2. These results imply that CO2 can be sequestered by a direct aqueous mineral carbonation using waste slate.

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

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Jinfu, E-mail: liang.shi2007@163.com [The Key Laboratory of Modern Acoustics, Ministry of Education, Institution of Acoustics, Nanjing University, Nanjing 210093 (China); School of Physics and Electronic Science, Guizhou Normal University, Guiyang 550001 (China); Chen, Weizhong, E-mail: wzchen@nju.edu.cn [The Key Laboratory of Modern Acoustics, Ministry of Education, Institution of Acoustics, Nanjing University, Nanjing 210093 (China); Zhou, Chao; Cui, Weicheng; Chen, Zhan [The Key Laboratory of Modern Acoustics, Ministry of Education, Institution of Acoustics, Nanjing University, Nanjing 210093 (China)

    2015-02-20

    Line emissions of trivalent terbium (Tb{sup 3+}) ion were observed from single-bubble sonoluminescence (SL) in an aqueous solution of terbium chloride (TbCl{sub 3}) 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{sup −}, Br{sup −}, and I{sup −}, 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.

  16. Condensation of Self-Assembled Lyotropic Chromonic Liquid Crystal Sunset Yellow in Aqueous Solutions Crowded with Polyethylene Glycol and Doped with Salt

    Energy Technology Data Exchange (ETDEWEB)

    Park, Heung-Shik; Kang, Shin-Woong; Tortora, Luana; Kumar, Satyendra; Lavrentovich, Oleg D. (Chonbuk); (Kent)

    2012-10-10

    We use optical and fluorescence microscopy, densitometry, cryo-transmission electron microscopy (cryo-TEM), spectroscopy, and synchrotron X-ray scattering to study the phase behavior of the reversible self-assembled chromonic aggregates of an anionic dye Sunset Yellow (SSY) in aqueous solutions crowded with an electrically neutral polymer polyethylene glycol (PEG) and doped with the salt NaCl. PEG causes the isotropic SSY solutions to condense into a liquid-crystalline region with a high concentration of SSY aggregates, coexisting with a PEG-rich isotropic (I) region. PEG added to the homogeneous nematic (N) phase causes separation into the coexisting N and I domains; the SSY concentration in the N domains is higher than the original concentration of PEG-free N phase. Finally, addition of PEG to the highly concentrated homogeneous N phase causes separation into the coexisting columnar hexagonal (C) phase and I phase. This behavior can be qualitatively explained by the depletion (excluded volume) effects that act at two different levels: at the level of aggregate assembly from monomers and short aggregates and at the level of interaggregate packing. We also show a strong effect of a monovalent salt NaCl on phase diagrams that is different for high and low concentrations of SSY. Upon the addition of salt, dilute I solutions of SSY show appearance of the condensed N domains, but the highly concentrated C phase transforms into a coexisting I and N domains. We suggest that the salt-induced screening of electric charges at the surface of chromonic aggregates leads to two different effects: (a) increase of the scission energy and the contour length of aggregates and (b) decrease of the persistence length of SSY aggregates.

  17. Phase Diagrams of the Aqueous Two-Phase Systems of Poly(ethylene glycol/Sodium Polyacrylate/Salts

    Directory of Open Access Journals (Sweden)

    Adalberto Pessoa Junior

    2011-03-01

    Full Text Available Aqueous two-phase systems consisting of polyethylene glycol (PEG, sodium polyacrylate (NaPAA, and a salt have been studied. The effects of the polymer size, salt type (NaCl, Na2SO4, sodium adipate and sodium azelate and salt concentrations on the position of the binodal curve were investigated. The investigated PEG molecules had a molar mass of 2,000 to 8,000 g/mol, while that of NaPAA was 8,000 g/mol. Experimental phase diagrams, and tie lines and calculated phase diagrams, based on Flory-Huggins theory of polymer solutions are presented. Due to strong enthalpic and entropic balancing forces, the hydrophobicity of the added salt has a strong influence on the position of the binodal, which could be reproduced by model calculations.

  18. Extraction of amylase from fermentation broth in poly (Ethylene Glycol salt aqueous two-phase system

    Directory of Open Access Journals (Sweden)

    Raquel Pedrosa Bezerra

    2006-07-01

    Full Text Available Studies were carried out on the partition of amylase from Bacillus subtilis in a minimal medium at 37 ºC and 110 rpm. Enzyme recovery was carried out in aqueous two-phase system PEG-Phosphate salt were carried out. The best purification factor (5.4 was obtained in system PEG 1000 (16.7% w/w with potassium phosphate (14.8% w/w, at pH 6.0, resulting in a recovery of 45.2% activity enzymatic in the salt-rich phase.Enzimas amilolíticas têm sido amplamente investigadas com a finalidade de melhorar os processos industriais para a degradação do amido. Foi determinado que a extração da enzima em sistema bifásico aquosos é um método aplicável para separação e purificação de biomoléculas em misturas. Vários sistemas compostos de soluções aquosas de polietilenoglicol e fosfato foram avaliados. Estudos de produção em meio mínimo suplementado, à 37ºC, com uma velocidade de agitação de 110rpm e recuperação da amilase a partir do Bacillus subtilis em sistema bifásico aquoso PEG-fosfato foram avaliados. O melhor fator de purificação (5.4 foi obtido no sistema PEG 1000 (16.7% w/w com fosfato de potássio (14.8% w/w, a pH 6.0, resultando na recuperação da atividade enzimática de 45.2% na fase rica em sal.

  19. Ca(OH)2-Catalyzed Condensation of Aldehydes with Methyl ketones in Dilute Aqueous Ethanol: A Comprehensive Access to α,β-Unsaturated Ketones

    Science.gov (United States)

    Yu, Lei; Han, Mengting; Luan, Jie; Xu, Lin; Ding, Yuanhua; Xu, Qing

    2016-01-01

    Cheap, abundant but seldom-employed Ca(OH)2 was found to be an excellent low-loading (5–10 mol%) catalyst for Claisen-Schmidt condensation of aldehydes with methyl ketones under mild conditions. It was interesting that dilute aqueous ethanol (20 v/v%) was unexpectedly discovered to be the optimal solvent. The reaction was scalable at least to 100 mmol and calcium could be precipitated by CO2 and removed by filtration. Evaporation of solvent directly afforded the product in the excellent 96% yield with high purity, as confirmed by its 1H NMR spectrum. PMID:27443482

  20. Structural transition in aqueous lipid/bile salt [DPPC/NaDC] supramolecular aggregates: SANS and DLS study

    Energy Technology Data Exchange (ETDEWEB)

    Kiselev, M.A. [Frank Laboratory of Neutron Physics, Joint Institute for Nuclear Research, Dubna (Russian Federation); Janich, M.; Hildebrand, A. [Martin-Luther-University, Halle (Saale) (Germany); Strunz, P. [Berlin Neutron Scattering Center, HZB, Berlin (Germany); Neubert, R.H.H. [Martin-Luther-University, Halle (Saale) (Germany); Lombardo, D., E-mail: lombardo@me.cnr.it [CNR–IPCF, Istituto per i Processi Chimico Fisici – (Sez. Messina), I-98158, Messina (Italy)

    2013-10-16

    Highlights: • Self-assembly in model DPPC lipids and NaDC bile salt by SANS and DLS experiments. • Bile salt creates structural interference against cohesive tendency of DPPC bilayers. • NaDC steric interactions cause transition toward different supramolecular structures. - Abstract: Small angle neutron scattering (SANS) and dynamic light scattering (DLS) were used to study different aggregation states in sodium deoxycholate (NaDC)-phosphatidylcholine systems at T = 60 °C. Size and shape of the aggregates investigated as a function of the NaDC bile salt concentration (at the constant DPPC concentration of 6 mM) indicate a strong dependence of the size and morphology of the generated aggregates on the relative amount of NaDC bile salt. More specifically large occupied area of the bile salt induces a steric interaction which promotes the transition toward a variety of supramolecular structures ranging from ellipsoidal vesicles, ribbon-like structures, up to final spherical mixed micelles at the large amount of bile salt of 10 mM NaDC. The findings of the obtained results give important insight for understanding the formation of different topologies in aqueous lipid–bile salt mixtures as well as stimulate new routes for liposome reconstitution–solubilisation processes suitable for technological applications.

  1. 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.

  2. Picosecond dynamics of proton transfer of a 7-hydroxyflavylium salt in aqueous-organic solvent mixtures.

    Science.gov (United States)

    Freitas, Adilson A; Quina, Frank H; Maçanita, António A L

    2011-10-13

    The intermediacy of the geminate base-proton pair (A*···H(+)) in excited-state proton-transfer (ESPT) reactions (two-step mechanism) has been investigated employing the synthetic flavylium salt 7-hydroxy-4-methyl-flavylium chloride (HMF). In aqueous solution, the ESPT mechanism involves solely the excited acid AH(+)* and base A* forms of HMF as indicated by the fluorescence spectra and double-exponential fluorescence decays (two species, two decay times). However, upon addition of either 1,4-dioxane or 1,2-propylene glycol, the decays become triple-exponential with a term consistent with the presence of the geminate base-proton pair A*···H(+). The geminate pair becomes detectable because of the increase in the recombination rate constant, k(rec), of (A*···H(+)) with increasing the mole fraction of added organic cosolvent. Because the two-step ESPT mechanism splits the intrinsic prototropic reaction rates (deprotonation of AH(+)*, k(d), and recombination, k(rec), of A*···H(+)) from the diffusion controlled rates (dissociation, k(diss), and formation, k(diff)[H(+)], of A*···H(+)), the experimental detection of the geminate pair provides a wealth of information on the proton-transfer reaction (k(d) and k(rec)) as well as on proton diffusion/migration (k(diss) and k(diff)).

  3. Formation and shape-control of hierarchical cobalt nanostructures using quaternary ammonium salts in aqueous media

    Science.gov (United States)

    Deshmukh, Ruchi; Mehra, Anurag

    2017-01-01

    Aggregation and self-assembly are influenced by molecular interactions. With precise control of molecular interactions, in this study, a wide range of nanostructures ranging from zero-dimensional nanospheres to hierarchical nanoplates and spindles have been successfully synthesized at ambient temperature in aqueous solution. The nanostructures reported here are formed by aggregation of spherical seed particles (monomers) in presence of quaternary ammonium salts. Hydroxide ions and a magnetic moment of the monomers are essential to induce shape anisotropy in the nanostructures. The cobalt nanoplates are studied in detail, and a growth mechanism based on collision, aggregation, and crystal consolidation is proposed based on a electron microscopy studies. The growth mechanism is generalized for rods, spindles, and nearly spherical nanostructures, obtained by varying the cation group in the quaternary ammonium hydroxides. Electron diffraction shows different predominant lattice planes on the edge and on the surface of a nanoplate. The study explains, hereto unaddressed, the temporal evolution of complex magnetic nanostructures. These ferromagnetic nanostructures represent an interesting combination of shape anisotropy and magnetic characteristics.

  4. Viscosities of oxalic acid and its salts in water and binary aqueous mixtures of tetrahydrofuran at different temperatures

    Indian Academy of Sciences (India)

    M L Parmar; M K Guleria

    2005-07-01

    Relative viscosities for the solutions of oxalic acid and its salts, viz. ammonium oxalate, sodium oxalate and potassium oxalate, at different concentrations have been determined in water and in binary aqueous mixtures of tetrahydrofuran (THF) [5, 10, 15 and 20% by weight of THF] at 298.15 K, and in water and in 5% (w/w) THF + water at five different temperatures. The data have been evaluated using the Jones-Dole equation and the obtained parameters have been interpreted in terms of solute-solute and solute-solvent interactions. The activation parameters of viscous flow have been obtained which depicts the mechanism of viscous flow. The oxalic acid and its salts behave as structure breakers in water and in binary aqueous mixtures of THF.

  5. Salt effect on the (polyethylene glycol 8000 + sodium sulfate) aqueous two-phase system: Relative hydrophobicity of the equilibrium phases

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Luisa A., E-mail: laferreira@deb.uminho.pt [IBB - Institute for Biotechnology and Bioengineering, Centre for Biological Engineering, Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Teixeira, Jose A. [IBB - Institute for Biotechnology and Bioengineering, Centre for Biological Engineering, Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal)

    2011-08-15

    Highlights: > Gibbs free energy of transfer of a methylene group on PEG 8000 - Na{sub 2}SO{sub 4} ATPS. > Influence of salt additive on the hydrophobic character of the coexisting phases. > Partitioning behavior of a series of five sodium salts of DNP-amino acids. > A relationship between {Delta}G(CH{sub 2}), TLL and I of the salt additive was established. - Abstract: The relative hydrophobicity of the phases of several {l_brace}polyethylene glycol (PEG) 8000 + sodium sulfate (Na{sub 2}SO{sub 4}){r_brace} aqueous two-phase systems (ATPSs), all containing 0.01 mol . L{sup -1} sodium phosphate buffer (NaPB, pH 7.4) and increasing concentration of a salt additive, NaCl or KCl, up to 1.0 mol . L{sup -1}, was measured by the free energy of transfer of a methylene group between the phases, {Delta}G(CH{sub 2}). The {Delta}G(CH{sub 2}) of the systems was determined by partitioning of a homologous series of five sodium salts of dinitrophenylated (DNP) - amino acids with aliphatic side chains in three different tie-lines of each biphasic system. The relative hydrophobicity of the phases ranged from -0.125 to -0.183 kcal . mol{sup -1}, being the NaCl salt the one to provide the more effective changes. The results show that, within each system, there is a linear relationship between the {Delta}G(CH{sub 2}) and the tie-line length (TLL), and biphasic systems with high salt additive concentration present the most negative {Delta}G(CH{sub 2}) values. Therefore, the feasibility of establishing a relationship between the relative hydrophobicity of the phases in a given TLL and the ionic strength of the salt additive was investigated and a satisfactory correlation was found for each salt.

  6. Effective enzymatic in situ saccharification of bamboo shoot shell pretreated by dilute alkalic salts sodium hypochlorite/sodium sulfide pretreatment under the autoclave system.

    Science.gov (United States)

    Chong, Gang-Gang; He, Yu-Cai; Liu, Qiu-Xiang; Kou, Xiao-Qin; Huang, Xiao-Jun; Di, Jun-Hua; Ma, Cui-Luan

    2017-10-01

    In this study, dilute alkali salts (0.6% NaClO, 0.067% Na2S) pretreatment at 10% sulfidity under the autoclave system at 120°C for 40min was used for pretreating bamboo shoot shell (BSS). Furthermore, FT-IR, XRD and SEM were employed to characterize the changes in the cellulose structural characteristics (porosity, morphology, and crystallinity) of the pretreated BSS solid residue. After 72h, the reducing sugars and glucose from the enzymatic in situ hydrolysis of 50g/L pretreated BSS in dilute NaClO/Na2S media could be obtained at 31.11 and 20.32g/L, respectively. Finally, the obtained BSS-hydrolysates containing alkalic salt NaClO/Na2S resulted in slightly negative effects on the ethanol production. Glucose in BSS-hydrolysates was fermented from 20.0 to 0.17g/L within 48h, and an ethanol yield of 0.41g/g glucose, which represents 80.1% of the theoretical yield, was obtained. This study provided an effective strategy for potential utilization of BSS. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Cloud Point and Liquid-Liquid Equilibrium Behavior of Thermosensitive Polymer L61 and Salt Aqueous Two-Phase System.

    Science.gov (United States)

    Rao, Wenwei; Wang, Yun; Han, Juan; Wang, Lei; Chen, Tong; Liu, Yan; Ni, Liang

    2015-06-25

    The cloud point of thermosensitive triblock polymer L61, poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO), was determined in the presence of various electrolytes (K2HPO4, (NH4)3C6H5O7, and K3C6H5O7). The cloud point of L61 was lowered by the addition of electrolytes, and the cloud point of L61 decreased linearly with increasing electrolyte concentration. The efficacy of electrolytes on reducing cloud point followed the order: K3C6H5O7 > (NH4)3C6H5O7 > K2HPO4. With the increase in salt concentration, aqueous two-phase systems exhibited a phase inversion. In addition, increasing the temperature reduced the concentration of salt needed that could promote phase inversion. The phase diagrams and liquid-liquid equilibrium data of the L61-K2HPO4/(NH4)3C6H5O7/K3C6H5O7 aqueous two-phase systems (before the phase inversion but also after phase inversion) were determined at T = (25, 30, and 35) °C. Phase diagrams of aqueous two-phase systems were fitted to a four-parameter empirical nonlinear expression. Moreover, the slopes of the tie-lines and the area of two-phase region in the diagram have a tendency to rise with increasing temperature. The capacity of different salts to induce aqueous two-phase system formation was the same order as the ability of salts to reduce the cloud point.

  8. Growth mechanism of a gas clathrate hydrate from a dilute aqueous gas solution: a molecular dynamics simulation of a three-phase system.

    Science.gov (United States)

    Nada, Hiroki

    2006-08-24

    A molecular dynamics simulation of a three-phase system including a gas clathrate, liquid water, and a gas was carried out at 298 K and high pressure in order to investigate the growth mechanism of the clathrate from a dilute aqueous gas solution. The simulation indicated that the clathrate grew on interfaces between the clathrate and the liquid water, after transfer of the gas molecules from the gas phase to the interfaces. The results suggest a two-step process for growth: first, gas molecules are arranged at cage sites, and second, H(2)O molecules are ordered near the gas molecules. The results also suggest that only the H(2)O molecules, which are surrounded or sandwiched by the gas molecules, form the stable polygons that constitute the cages of the clathrate. In addition, the growth of the clathrate from a concentrated aqueous gas solution was also simulated, and the results suggested a growth mechanism in which many H(2)O and gas molecules correctively form the structure of the clathrate. The clathrate grown from the concentrated solution contained some empty cages, whereas the formation of empty cages was not observed during the growth from the dilute solution. The results obtained by both simulations are compared with the results of an experimental study, and the growth mechanism of the clathrate in a real system is discussed.

  9. Molecular properties and intermolecular forces--factors balancing the effect of carbon surface chemistry in adsorption of organics from dilute aqueous solutions.

    Science.gov (United States)

    Terzyk, Artur P

    2004-07-01

    Presented paper recapitulates the results of 6 years' study concerning the effect of carbon surface chemical composition on adsorption of paracetamol, phenol, acetanilide, and aniline from dilute aqueous solutions on carbons. Adsorption-desorption isotherms, enthalpy, and kinetics of adsorption data are shown for the measurements performed at three temperatures (300, 310, and 320 K) at two pH levels (1.5 and 7) on commercial activated carbons. The data were obtained for four carbons: the initial carbon D43/1 and forms modified by applying concentrated HNO3, fuming H2SO4, and gaseous NH3. The modification procedures do not change the porosity in a drastic way, but lead to drastic changes of the composition of carbon surface layer. By applying MOPAC (a general-purpose semiempirical molecular orbital package), the physicochemical constants characterizing the molecules of adsorbates are calculated, including the distribution of the Mulliken charges, the dipole moments and ionization potentials, and the energies of interaction with the unique positive and negative charges. They are correlated with the parameters characterizing the adsorption (and kinetics) process of studied molecules on the mentioned above carbons. The mechanisms proposed in the literature for the description of adsorption from dilute aqueous solutions are verified, and a general mechanism of adsorption is proposed.

  10. 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:

  11. Salt-enhanced removal of 2-ethyl-1-hexanol from aqueous solutions by adsorption on activated carbon.

    Science.gov (United States)

    Chang, Ganggang; Bao, Zongbi; Zhang, Zhiguo; Xing, Huabin; Su, Baogen; Yang, Yiwen; Ren, Qilong

    2013-12-15

    2-Ethyl-1-hexanol has extensive industrial applications in solvent extraction, however, in view of its potential pollution to environment, the removal and recovery of 2-ethyl-1-hexanol is considered an essential step toward its sustainable use in the future. In this work, we report the removal of 2-ethyl-1-hexanol from aqueous solutions containing salts in high concentrations by adsorption on a coal-based activated carbon. Adsorption thermodynamics showed that the experimental isotherms were conformed well to the Langmuir equation. Also it was found that inorganic salts, i.e. MgCl2 and CaCl2 in high concentration significantly enhanced the adsorption capacity from 223 mg/g in the deionized water to 277 mg/g in a saline water. This phenomenon of adsorption enhancement could be ascribed to the salt-out effect. Kinetic analysis indicated that adsorption kinetics follows the pseudo-second-order equation and the adsorption rate constants increase with the salt concentration. The dynamic breakthrough volume and adsorbed amount of 2-ethyl-1-hexanol were significantly elevated when the salt is present in the water. The dynamic saturated adsorption amount increased from 218.3mg/g in the deionized water to 309.5mg/g in a salt lake brine. The Tomas model was well applied to predict the breakthrough curves and determine the characteristics parameters of the adsorption column.

  12. Measurement and Correlation of Partition Coefficients of Baicalin in EOPO/Salt Aqueous Two-Phase Systems

    Institute of Scientific and Technical Information of China (English)

    李伟; 朱自强

    2002-01-01

    The partition coefficients of baicalin were measured in ethylene oxide and propylene oxide(EOPO)/salt aqueous two-phase systems at 298.15K,It was found that most of baicalin partitioned into EOPO-rich phase.The partition coefficients of baicalin varied from 10 to 120.The effect of various factors,including tie-line lngth,salt composition,molecular weight of EOPO,and solution pH,on the partition behavior was investigated on EOPO/salt systems.Furthermore the partition coefficients of baicalin were correlated using the modified Diamond-Hsu model.Good agreement with experimental data is obtained.The average relative deviations are less than 5.0%.

  13. Effect of ethanol, temperature, and gas flow rate on volatile release from aqueous solutions under dynamic headspace dilution conditions.

    Science.gov (United States)

    Tsachaki, Maroussa; Gady, Anne-Laure; Kalopesas, Michalis; Linforth, Robert S T; Athès, Violaine; Marin, Michele; Taylor, Andrew J

    2008-07-09

    On the basis of a mechanistic model, the overall and liquid mass transfer coefficients of aroma compounds were estimated during aroma release when an inert gas diluted the static headspace over simple ethanol/water solutions (ethanol concentration = 120 mL x L(-1)). Studied for a range of 17 compounds, they were both increased in the ethanol/water solution compared to the water solution, showing a better mass transfer due to the presence of ethanol, additively to partition coefficient variation. Thermal imaging results showed differences in convection of the two systems (water and ethanol/water) arguing for ethanol convection enhancement inside the liquid. The effect of ethanol in the solution on mass transfer coefficients at different temperatures was minor. On the contrary, at different headspace dilution rates, the effect of ethanol in the solution helped to maintain the volatile headspace concentration close to equilibrium concentration, when the headspace was replenished 1-3 times per minute.

  14. Surface tension of dilute alcohol-aqueous binary fluids: n-Butanol/water, n-Pentanol/water, and n-Hexanol/water solutions

    Science.gov (United States)

    Cheng, Kuok Kong; Park, Chanwoo

    2017-01-01

    Surface tension of pure fluids, inherently decreasing with regard to temperature, creates a thermo-capillary-driven (Marangoni) flow moving away from a hot surface. It has been known that few high-carbon alcohol-aqueous solutions exhibit an opposite behavior of the surface tension increasing with regard to temperature, such that the Marangoni flow moves towards the hot surface (self-rewetting effect). We report the surface tensions of three dilute aqueous solutions of n-Butanol, n-Pentanol and n-Hexanol as self-rewetting fluids measured for ranges of alcohol concentration (within solubility limits) and fluid temperatures (25-85 °C). A maximum bubble pressure method using a leak-tight setup was used to measure the surface tension without evaporation losses of volatile components. It was found from this study that the aqueous solutions with higher-carbon alcohols exhibit a weak self-rewetting behavior, such that the surface tensions remain constant or slightly increases above about 60 °C. These results greatly differ from the previously reported results showing a strong self-rewetting behavior, which is attributed to the measurement errors associated with the evaporation losses of test fluids during open-system experiments.

  15. Determination of the osmotic second virial coefficient and the demerization of beta-lactoglobulin in aqueous solutions with added salt at the isoelectric point

    NARCIS (Netherlands)

    Schaink, H.M.; Smit, J.A.M.

    2000-01-01

    Aqueous solutions of β-lactoglobulin (at the isoelectric point pH=5.18) have been studied by membrane osmometry. The osmotic second virial coefficient as well as the monomer–dimer equilibrium of β-lactoglobulin have been found to depend significantly on the salt concentration. At low salt

  16. Extended UNIQUAC Model for Correlation and Prediction of Vapor-Liquid-Liquid-Solid Equilibria in Aqueous Salt Systems Containing Non-Electrolytes. Part B. Alcohol (Ethanol, Propanols, Butanols) - Water-salt systems

    DEFF Research Database (Denmark)

    Thomsen, Kaj; Iliuta, Maria Cornelia; Rasmussen, Peter

    2004-01-01

    -Redlich-Kwong equation of state. The model only requires binary, temperature-dependent interaction parameters. It has previously been used to describe the excess Gibbs energy for aqueous electrolyte mixtures and aqueous electrolyte systems containing methanol. It has been found to be an adequate model for representing...... solid-liquid-vapor equilibrium and thermal property data for strongly non-ideal systems. In this work, the model is extended to aqueous salt systems containing higher alcohols. The calculations are based on an extensive database consisting of salt solubility data, vapor liquid equilibrium data...

  17. Aqueous singlet oxygen reaction kinetics of furfuryl alcohol: effect of temperature, pH, and salt content.

    Science.gov (United States)

    Appiani, Elena; Ossola, Rachele; Latch, Douglas E; Erickson, Paul R; McNeill, Kristopher

    2017-02-28

    The rate constant for the reaction between furfuryl alcohol (FFA) and singlet oxygen ((1)O2) in aqueous solution was measured as a function of temperature, pH and salt content employing both steady-state photolysis (β value determination) and time-resolved singlet oxygen phosphorescence methods. The latter provided more precise and reproducible data. The reaction rate constant, krxn,FFA, had a relatively small temperature dependence, no pH dependence and showed a small increase in the presence of high salt concentrations (+19% with 1 M NaCl). A critical review of the available literature suggested that the widely used value of 1.2 × 10(8) M(-1) s(-1) is likely overestimated. Therefore, we recommend the use of 1.00 × 10(8) M(-1) s(-1) for reactions performed in low ionic strength aqueous solutions (freshwater) at 22 °C. Furthermore, corrections are provided that should be applied when working at higher or lower temperatures, and/or at high salt concentrations (seawater).

  18. 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.

  19. Diclofenac Salts, VIII. Effect of the Counterions on the Permeation through Porcine Membrane from Aqueous Saturated Solutions

    Directory of Open Access Journals (Sweden)

    Cristina Cavallari

    2012-09-01

    Full Text Available The following bases: monoethylamine (EtA, diethylamine (DEtA, triethylamine (TEtA, monoethanolamine (MEA, diethanolamine (DEA, triethanolamine (TEA, pyrrolidine (Py, piperidine (Pp, morpholine (M, piperazine (Pz and their N-2-hydroxyethyl (HE analogs were employed to prepare 14 diclofenac salts. The salts were re-crystallized from water in order to obtain forms that are stable in the presence of water. Vertical Franz-type cells with a diffusional surface area of 9.62 cm2 were used to study the permeation of these diclofenac salts from their saturated solutions through an internal pig ear membrane. The receptor compartments of the cells contained 100 mL of phosphate buffer (pH 7.4; a saturated solution (5 mL of each salt was placed in the donor compartment, thermostated at 37 °C. Aliquots were withdrawn at predetermined time intervals over 8 h and then immediately analyzed by HPLC. Fluxes were determined by plotting the permeated amount, normalized for the membrane surface area versus time. Permeation coefficients were obtained dividing the flux values J by the concentration of the releasing phase—that is, water solubility of each salt. Experimental results show that fluxes could be measured when diclofenac salts with aliphatic amines are released from a saturated aqueous solution. Different chemical species (acid, anion, ion pairs contribute to permeation of the anti-inflammatory agent even though ion-pairs could be hypothesized to operate to a greater extent. Permeation coefficients were found higher when the counterion contains a ring; while hydroxy groups alone do not appear to play an important role, the ring could sustain permeation, disrupting the organized domains of the membrane.

  20. Aspartic acid interaction with cobalt(II) in dilute aqueous solution: A 57Co emission Mössbauer spectroscopic study

    Science.gov (United States)

    Kamnev, Alexander A.; Tugarova, Anna V.; Kovács, Krisztina; Homonnay, Zoltan; Kuzmann, Erno; Vértes, Attila

    2012-03-01

    Emission (57Co) Mössbauer spectra of the aspartic acid—57CoCl2 system were measured at T = 80 K in frozen aqueous solution and in the form of a dried residue of this solution. The Mössbauer spectra, besides a weak contribution from after-effects, showed two Fe2 + /Co2 + components which were ascribed to octahedrally and tetrahedrally coordinated 57CoII microenvironments in the Asp-cobalt(II) complex. This dual coordination mode may be due to the involvement of the second terminal carboxylic group of aspartic acid in the coordination sphere of Co.

  1. Aspartic acid interaction with cobalt(II) in dilute aqueous solution: A {sup 57}Co emission Moessbauer spectroscopic study

    Energy Technology Data Exchange (ETDEWEB)

    Kamnev, Alexander A.; Tugarova, Anna V. [Institute of Biochemistry and Physiology of Plants and Microorganisms, Russian Academy of Sciences (Russian Federation); Kovacs, Krisztina; Homonnay, Zoltan, E-mail: homonnay@ludens.elte.hu; Kuzmann, Erno; Vertes, Attila [Eoetvoes Lorand University, Institute of Chemistry (Hungary)

    2012-03-15

    Emission ({sup 57}Co) Moessbauer spectra of the aspartic acid-{sup 57}CoCl{sub 2} system were measured at T = 80 K in frozen aqueous solution and in the form of a dried residue of this solution. The Moessbauer spectra, besides a weak contribution from after-effects, showed two Fe{sup 2 + }/Co{sup 2 + } components which were ascribed to octahedrally and tetrahedrally coordinated {sup 57}Co{sup II} microenvironments in the Asp-cobalt(II) complex. This dual coordination mode may be due to the involvement of the second terminal carboxylic group of aspartic acid in the coordination sphere of Co.

  2. Partitioning of L-methionine in aqueous two-phase systems containing poly(propylene glycol) and sodium phosphate salts

    Energy Technology Data Exchange (ETDEWEB)

    Salabat, Alireza, E-mail: a-salabat@araku.ac.ir [Chemistry Department, Arak University, P.O. Box 38156-879, Arak (Iran, Islamic Republic of); Sadeghi, Rahmat [Department of Chemistry, University of Kurdistan, Sanandaj, Kurdistan 66135 (Iran, Islamic Republic of); Moghadam, Somayeh Tiani [Chemistry Department, Arak University, P.O. Box 38156-879, Arak (Iran, Islamic Republic of); Jamehbozorg, Bahman [Department of Chemistry, University of Kurdistan, Sanandaj, Kurdistan 66135 (Iran, Islamic Republic of)

    2011-10-15

    Highlights: > Thermodynamics parameters for partitioning of L-methionine in ATPS. > Investigation of different effects on partition coefficient of the amino acid. > Propose the best condition for L-methionine partitioning. - Abstract: The partitioning behavior of L-methionine has been studied in aqueous two-phase systems of (poly(propylene glycol) + sodium phosphate salts + H{sub 2}O) at different temperatures. The salts used were sodium di-hydrogen phosphate (NaH{sub 2}PO{sub 4}), di-sodium hydrogen phosphate (Na{sub 2}HPO{sub 4}) and tri-sodium phosphate (Na{sub 3}PO{sub 4}). The effects of tie line length, salt type, and temperature on the partition coefficient of this amino acid have been studied. In addition, thermodynamic parameters ({Delta}H{sup o}, {Delta}S{sup o} and {Delta}G{sup o}) as a function of temperature were calculated. The results showed that increasing tie line length led to decreasing of the partition coefficient. We also showed that the partition coefficients of the amino acid in the systems containing Na{sub 3}PO{sub 4} are greater than the other two salts. Moreover, it is verified that increasing temperature led to decreasing the partition coefficient. The experimental partition coefficient data are correlated using a modified virial-type model.

  3. 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.

  4. Density, Viscosity, Solubility, and Diffusivity of N2O in Aqueous Amino Acid Salt Solutions

    NARCIS (Netherlands)

    Kumar, P. Senthil; Hogendoorn, J.A.; Feron, P.H.M.; Versteeg, G.F.

    2001-01-01

    Solubility and diffusivity of N2O in aqueous solutions of potassium taurate are reported over a wide range of concentration and temperature. Also, the solubility of N2O in aqueous potassium glycinate solution is reported at 295 K. The ion specific constants are reported for taurate and glycinate ani

  5. DILUTE SOLUTION BEHAVIOR OF CHITOSAN IN DIFFERENT ACID SOLVENTS

    Institute of Scientific and Technical Information of China (English)

    WANG Wei; WANG Lihua; QIN Wen

    1994-01-01

    Dilute solution behavior of chitosan was studied in formic acid, acetic acid,lactic acid and hydrochloric acid aqueous solution under different pH values. The reduced viscosities, ηsp/C,of chitosan solutions were dependent on the properties of acid and pH value of solvents. For a given chitosan concentration, ηsp/C decreased with the increase of acid concentration, or decreasing pH of solvent, indicating shielding effect of excessive acid similar to adding salt into solution. The stabilities of dilute chitosan solution in formic acid and lactic acid were better than that in acetic acid and hydrochloric acid.

  6. Adsorption and reduction: combined effect of polyaniline emeraldine salt for removal of Cr(VI) from aqueous medium

    Indian Academy of Sciences (India)

    PURNIMA BARUAH; DEBAJYOTI MAHANTA

    2016-06-01

    In this study, we have reported the removal of Cr(VI) ions by polyaniline (PANI) particles from aqueous medium. PANI in its emeraldine salt (ES) form can interact with Cr(VI), which is present as HCrO$^{−}_4$ in two ways. The adsorption of HCrO$^{−}_4$ ions due to the electrostatic interaction between partially positively charged PANI backbone and Cr(VI) anions causes the major portion of Cr(VI) removal and a small portion of Cr(VI) is reduced to Cr(III) by PANI (ES). The adsorption follows Langmuir adsorption isotherm and second-order kinetic model. It is observed that the removal of Cr(VI) is negligibly effected by the presence of other anions in the aqueous medium. The adsorption capacity of PANI (ES) is found to be 123 mg g$^{−1}$, which is very high compared to activated carbonbased materials. The adsorbed anions can be desorbed by converting PANI emeraldine salt (ES) to PANI emeraldinebase (EB). The EB form of PANI can be converted into ES form by treating with acid, which can be reused as adsorbent. It is important to note that the PANI (ES) is oxidized by HCrO$^{−}_4$ ions which decrease the hydrophilicity of thesurface of PANI particles. This causes the decrease in adsorption capacity of recycled PANI.

  7. Hydroxyl radical-induced crosslinking and radiation-initiated hydrogel formation in dilute aqueous solutions of carboxymethylcellulose.

    Science.gov (United States)

    Wach, Radoslaw A; Rokita, Bozena; Bartoszek, Nina; Katsumura, Yosuke; Ulanski, Piotr; Rosiak, Janusz M

    2014-11-04

    Ionizing radiation causes chain scission of polysaccharides in the absence of crosslinking agents. It has been demonstrated before that degradation of carboxyalkylated polysaccharides may be prevented, despite presence of strong electrostatic repulsing forces between chains, at very high polymer concentration in water (paste-like state) when physical proximity promotes recombination of radiation-generated polymer radicals. In such conditions, crosslinking dominates over chain scission and covalent, macroscopic gels can be formed. In an approach proposed in this work, neutralizing the charges on carboxymethylcellulose (CMC) by lowering the pH results in retracting the electrostatic repulsion between chain segments and thus allows for substantial reduction of polymer concentration required to achieve gelation due to domination of crosslinking reactions. Electron-beam irradiation of aqueous solutions of low pH containing 0.5-2% CMC results in hydrogel formation with 70% yield, while both concentration and dose determine their swelling properties. Time-resolved studies by laser flash photolysis clearly indicate strong pH influence on decay kinetics of CMC radicals.

  8. 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.

  9. Pretreatment of Dried Distiller Grains with Solubles by Soaking in Aqueous Ammonia and Subsequent Enzymatic/Dilute Acid Hydrolysis to Produce Fermentable Sugars.

    Science.gov (United States)

    Nghiem, Nhuan P; Montanti, Justin; Kim, Tae Hyun

    2016-05-01

    Dried distillers grains with solubles (DDGS), a co-product of corn ethanol production in the dry-grind process, was pretreated by soaking in aqueous ammonia (SAA) using a 15 % w/w NH4OH solution at a solid/liquid ratio of 1:10. The effect of pretreatment on subsequent enzymatic hydrolysis was studied at two temperatures (40 and 60 °C) and four reaction times (6, 12, 24, and 48 h). Highest glucose yield of 91 % theoretical was obtained for the DDGS pretreated at 60 °C and 24 h. The solubilized hemicellulose in the liquid fraction was further hydrolyzed with dilute H2SO4 to generate fermentable monomeric sugars. The conditions of acid hydrolysis included 1 and 4 wt% acid, 60 and 120 °C, and 0.5 and 1 h. Highest yields of xylose and arabinose were obtained at 4 wt% acid, 120 °C, and 1 h. The fermentability of the hydrolysate obtained by enzymatic hydrolysis of the SAA-pretreated DDGS was demonstrated in ethanol fermentation by Saccharomyces cerevisiae. The fermentability of the hydrolysate obtained by consecutive enzymatic and dilute acid hydrolysis was demonstrated using a succinic acid-producing microorganism, strain Escherichia coli AFP184. Under the fermentation conditions, complete utilization of glucose and arabinose was observed, whereas only 47 % of xylose was used. The succinic acid yield was 0.60 g/g total sugar consumed.

  10. [Aqueous and salt solutions of quinine of low concentrations: self-organization, physicochemical properties and actions on the electrical characteristics of neurons].

    Science.gov (United States)

    Murtazina, L I; Ryzhkina, I S; Mishina, O A; Andrianov, V V; Bogodvid, T Kh; Gaĭnutdinov, Kh L; Muranova, L N; Konovalov, A I

    2014-01-01

    Self-organization, the physicochemical properties of aqueous and salt solutions of quinine and the effects of salt quinine solutions in a wide range of concentrations (1 x 10(-22) - 1 x 10(-3) M) on the electrical characteristics of the edible snail's identified neurons were studied. Similar non-monotonic concentration dependencies of physicochemical properties of aqueous and salt quinine solutions at low concentrations are obtained. This allows of predicting the occurrence of biological effects at low concentrations of quinine solutions. Intrinsic (within 5% of the interval) changes in membrane potential, the amplitude and duration of the neuron action potential under the influence of quinine salt solutions at concentrations of quinine of 1 x 10(-20), 1 x 10(-18), 1 x 10(-10) M are found. For these concentrations the extreme values of specific conductivity and pH are shown.

  11. Separation of compounds with multiple -OH groups from dilute aqueous solutions via complexation with organoboronate. [1,2-propanediol

    Energy Technology Data Exchange (ETDEWEB)

    Chow, Tina Kuo Fung.

    1992-05-01

    The complexing extractant agent investigated in this work is 3-nitrophenylboronic acid (NPBA) in its anionic form (NPB). NPBA and Aliquat 336 (quaternary amine) is dissolved in 2-ethyl-l-hexanol, and the extractant is contacted with aq. NaOH. Solutes investigated were 1,2-propanediol, glycerol, fructose, sorbitol and lactic acid. Batch extraction experiments were performed at 25{degree}C. Partition coefficients, distribution ratios and loadings are reported for varying concentrations of solute and NPB. All solutes complexed with NPB{sup {minus}}, with all complexes containing only one NPB{sup {minus}} per complex. The 1:1 complexation constants for the solutes glycerol, fructose and sorbitol follow trends similar to complexation with B(OH){sub 4}{sup {minus}} (aq.), i.e. the complexation constants increase with increasing number of {minus}OH groups available for complexation. Assumption of 1:1 complex is not valid for 1, 2-propanediol, which showed overloading (more than one mole of solute complexed to one mole NPB{sup {minus}}) at higher concentrations. The {minus}OH group on the NPB{sup {minus}} which is left uncomplexed after one solute molecule had bound to the other two {minus}OH groups may be responsible for the overloading. Overloading is also observed in extraction of tactic acid, but through a different mechanism. It was found that TOMA{sup +} can extract lactic acid to an extent comparable to the uptake of lactic acid by NPB{sup {minus}}. The complexation is probably through formation of an acid-base ion pair. Losses of NPBA into the aqueous phase could lead to problems, poor economics in industrial separation processes. One way of overcoming this problem would be to incorporate the NPBA onto a solid support.

  12. A Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation

    DEFF Research Database (Denmark)

    Bonalumi, Davide; Valenti, Gianluca; Lillia, Stefano

    2016-01-01

    Post-combustion carbon capture technologies seem to be necessary to realize the CO2 mitigation policies internationally shared for the next future, despite none of them appears to be ready for full-scale applications. This work considers the aqueous ammonia based process for a coal-fired Ultra...

  13. KINETICS OF THE HYDROXYETHYLATION OF STARCH IN ALKALINE SALT-CONTAINING AQUEOUS SLURRIES

    NARCIS (Netherlands)

    VANWARNERS, A; STAMNHUIS, EJ; BEENACKERS, AACM

    1994-01-01

    A two-phase kinetic model is presented for the base-catalyzed hydroxyethylation of potato starch using ethylene oxide at temperatures between 293 and 318 K in aqueous starch slurries containing sodium sulfate. The rate of the hydroxyethylation of starch as a function of starch anion concentration (c

  14. Free Energy Perturbation Monte Carlo Simulations of Salt Influences on Aqueous Freezing Point Depression

    Science.gov (United States)

    Dick, Thomas J.; Wierzbicki, Andrzej; Madura, Jeffry D.

    Free energy perturbation Monte Carlo (FEP/MC) simulations are performed for both the liquid and solid phases of water to determine the melting temperature of several popular three and four-site water models. Gibbs free energy vs. temperature plots are constructed from the simulations to determine the melting temperature. For the liquid phase, standard FEP/MC simulations are used to calculate the free energy relative to the gas phase at multiple temperatures. The free energy of the solid phase relative to the gas phase is calculated at multiple temperatures using the lattice-coupling method. The intersection of the free energy regression lines determines the estimate of the melting temperature. Additionally, simulations were carried out for simple salt solutions to determine the freezing point depressions (FPD). The simulations reproduce the FPD as a function of salt concentration for solutions of NaCl, KCl, CaCl2, and MgCl2.

  15. Ionic interactions. Subnanoscale hydrophobic modulation of salt bridges in aqueous media.

    Science.gov (United States)

    Chen, Shuo; Itoh, Yoshimitsu; Masuda, Takuya; Shimizu, Seishi; Zhao, Jun; Ma, Jing; Nakamura, Shugo; Okuro, Kou; Noguchi, Hidenori; Uosaki, Kohei; Aida, Takuzo

    2015-05-01

    Polar interactions such as electrostatic forces and hydrogen bonds play an essential role in biological molecular recognition. On a protein surface, polar interactions occur mostly in a hydrophobic environment because nonpolar amino acid residues cover ~75% of the protein surface. We report that ionic interactions on a hydrophobic surface are modulated by their subnanoscale distance to the surface. We developed a series of ionic head groups-appended self-assembled monolayers with C2, C6, C8, and C12 space-filling alkyl chains, which capture a dendritic guest via the formation of multiple salt bridges. The guest release upon protonolysis is progressively suppressed when its distance from the background hydrophobe changes from 1.2 (C2) to 0.2 (C12) nanometers, with an increase in salt bridge strength of ~3.9 kilocalories per mole.

  16. Behavior of gellan in aqueous-salt solutions and oilfield saline water

    Directory of Open Access Journals (Sweden)

    Zhanar Nurakhmetova

    2015-09-01

    Full Text Available The influence of storage time and temperature on the behavior of low acyl gellan (LAG was studied by viscometry and 1H NMR spectroscopy without salt addition. The viscometric results revealed that the effectiveness of salts to enhance gelation of gellan changes in the following order: BaСl2>CaCl2»MgCl2>KCl>NaCl. The sol-gel and liquid-solid phase transitions of gellan solutions were observed upon addition of oilfield water containing 73 g L-1 of alkaline and alkaline earth metal ions. The effectiveness of salts to induce the separation of liquid and solid phases changes in the sequence: NaCl>KCl>MgCl2»CaCl2»BaСl2. The hydrodynamic behavior of 0.5 wt.% gellan solution injected into the sand pack model with high (20 Darcy and lower (2 Darcy permeability is useful to model the oil reservoirs in the process of enhanced oil recovery.

  17. Solid-state materials for anion sensing in aqueous solution: highly selective colorimetric and luminescence-based detection of perchlorate using a platinum(II) salt.

    Science.gov (United States)

    Taylor, Stephen D; Howard, Whitney; Kaval, Necati; Hart, Robert; Krause, Jeanette A; Connick, William B

    2010-02-21

    The PF(6)(-) salt of a platinum(II) complex changes from yellow to red and becomes intensely luminescent upon exposure to aqueous ClO(4)(-). The response is remarkably selective. Spectroscopic changes are consistent with anion exchange resulting in shortening of the intramolecular PtPt distances between the square planar cations.

  18. Solid-state materials for anion sensing in aqueous solution: highly selective colorimetric and luminescence-based detection of perchlorate using a platinum(II) salt

    Energy Technology Data Exchange (ETDEWEB)

    Taylor, Stephen D.; Howard, Whitney; Kaval, Necati; Hart, Robert; Krause, Jeanette A.; Connick, William B. (UCIN); (Shepherd)

    2010-07-23

    The PF{sub 6}{sup -} salt of a platinum(II) complex changes from yellow to red and becomes intensely luminescent upon exposure to aqueous ClO{sub 4}{sup -}. The response is remarkably selective. Spectroscopic changes are consistent with anion exchange resulting in shortening of the intramolecular Pt***Pt distances between the square planar cations.

  19. A molecular dynamic study on the dissociation mechanism of SI methane hydrate in inorganic salt aqueous solutions.

    Science.gov (United States)

    Xu, Jiafang; Chen, Zhe; Liu, Jinxiang; Sun, Zening; Wang, Xiaopu; Zhang, Jun

    2017-08-01

    Gas hydrate is not only a potential energy resource, but also almost the biggest challenge in oil/gas flow assurance. Inorganic salts such as NaCl, KCl and CaCl2 are widely used as the thermodynamic inhibitor to reduce the risk caused by hydrate formation. However, the inhibition mechanism is still unclear. Therefore, molecular dynamic (MD) simulation was performed to study the dissociation of structure I (SI) methane hydrate in existence of inorganic salt aqueous solution on a micro-scale. The simulation results showed that, the dissociation became stagnant due to the presence of liquid film formed by the decomposed water molecules, and more inorganic ions could shorten the stagnation-time. The diffusion coefficients of ions and water molecules were the largest in KCl system. The structures of ion/H2O and H2O/H2O were the most compact in hydrate/NaCl system. The ionic ability to decompose hydrate cells followed the sequence of: Ca(2+)>2K(+)>2Cl(-)>2Na(+). Copyright © 2017 Elsevier Inc. All rights reserved.

  20. D{sub 2}O−H{sub 2}O solvent isotope effects on the enthalpies of bicaret hydration and dilution of its aqueous solutions at different temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Ivanov, Evgeniy V., E-mail: evi@isc-ras.ru [Laboratory of Thermodynamics of Solutions of Non-electrolytes and Biologically Active Substances, G.A. Krestov Institute of Solution Chemistry, Russian Academy of Sciences, 1 Akademicheskaya Str., 153045 Ivanovo (Russian Federation); Batov, Dmitriy V. [Incorporated Physicochemical Center of Solution Researches, G.A. Krestov Institute of Solution Chemistry, Russian Academy of Sciences, 1 Akademicheskaya Str., 153045, Ivanovo (Russian Federation); Ivanovo' s State University of Chemistry and Technology, 7 Sheremetevsky Ave, 153000 Ivanovo (Russian Federation); Gazieva, Galina A.; Kravchenko, Angelina N. [Laboratory of Nitrogen-containing Compounds, N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., 199119 Moscow (Russian Federation); Abrosimov, Vladimir K. [Laboratory of Thermodynamics of Solutions of Non-electrolytes and Biologically Active Substances, G.A. Krestov Institute of Solution Chemistry, Russian Academy of Sciences, 1 Akademicheskaya Str., 153045 Ivanovo (Russian Federation)

    2014-08-20

    Graphical abstract: - Highlights: • Enthalpies of solution of bicaret (tetraethylglycoluril) in H{sub 2}O and D{sub 2}O were measured. • D{sub 2}O–H{sub 2}O enthalpy-isotopic effect is negative and decreasing with temperature. • Enthalpic coefficients h{sub 22} for pairwise solute–solute interactions were derived. • Quantity of h{sub 22} is negative and becoming the more negative in heavy water. • Prevailingly hydrophobic hydration of bicaret is weakened with rising temperature. - Abstract: The molar enthalpies of solution of bicaret or 2,4,6,8-tetraethyl-2,4,6,8-tatraazabicyclo[3.3.0]octane-3,7-dione in ordinary (H{sub 2}O) and heavy (D{sub 2}O) water at (278.15, 288.15, 298.15, 308.15, and 318.15) K as well as the enthalpies for dilution of its H/D isotopically distinguishable aqueous solutions at 298.15 K were measured calorimetrically. The standard (at infinite dilution) molar enthalpies and heat capacities of solution, and the enthalpic coefficients for pair (h{sub 22}) and triplet (h{sub 222}) interactions between hydrated solute molecules, along with D{sub 2}O–H{sub 2}O solvent isotope effects (IEs) on the studied quantities were computed. The enthalpic effects of bicaret dissolution and corresponding IEs were found to be negative and decreasing in magnitude with increasing temperature. On the contrary, the h{sub 22} and h{sub 222} values as well as IEs on them were found to be positive. These facts indicate that the bicaret hydration being predominantly hydrophobic is enhanced in the D{sub 2}O medium. The hydration behavior of the solute considered was discussed in comparison with that for mebicar or 2,4,6,8-tetramethyl-2,4,6,8-tatraazabicyclo[3.3.0]octane-3,7-dione using the previously obtained data.

  1. Simultaneous determination of dorzolomide and timolol in aqueous humor: a novel salting out liquid-liquid microextraction combined with HPLC.

    Science.gov (United States)

    Mohamed, Abdel-Maaboud Ismail; Abdel-Wadood, Hanaa Mohammed; Mousa, Heba Salah

    2014-12-01

    A Snovel method for the simultaneous separation and determination of two antiglaucoma drugs namely, dorzolamide hydrochloride (DOR) and timolol maleate (TIM) in aqueous humor samples (AH) was developed by using salting-out assisted liquid-liquid microextraction (SALLME) combined with HPLC-UV method. Box-Behnken experimental design and response surface methodology were employed to assist the optimization of SALLME conditions, including salt concentration, the pH of sample solution and vortex time as variable factors. The optimal extraction conditions were as follows: to 50 µL of AH sample, 100 µL of phosphate buffer (100 mmol L(-1), pH 11.9), 90 µL of acetonitrile (ACN) and 0.11 g of (NH4)2SO4 salt were added into an Eppendorf vial (1 mL) then vortexed for 1.1 min. As an effort to miniaturize SALLE system, a 1 mL syringe adapted with a capillary tube was employed as the phase separation device. Once the phase separation occurred, the upper layer could be narrowed into the capillary tube by pushing the plunger; thus, the collection of the upper layer solvent was simple and convenient. By miniaturization, the consumption of the organic solvent was decreased as low as possible. The chromatographic separation was achieved on Gemini C18 column using a mobile phase of ACN: 30 mmol L(-1) potassium dihydrogen phosphate buffer containing 0.1% triethylamine, pH 3.5 (20:80, v/v) at a flow rate of 1 mL min(-1) and UV detection at 254 and 295 nm for DOR and TIM, respectively. Mepivacaine hydrochloride was used as an internal standard. The described method showed better separation with enhanced sensitivities than the previously reported methods with limits of quantitation of 8.75 and 10.32 ng mL(-1) in aqueous solution and 15.97 and 23.53 ng mL(-1) in AH for DOR and TIM, respectively. The simple, rapid and eco-friendly SALLME-HPLC method has been successfully applied for the simultaneous pharmacokinetic studies of DOR and TIM in rabbit AH.

  2. Hydration and ion pair formation in common aqueous La(III) salt solutions--a Raman scattering and DFT study.

    Science.gov (United States)

    Rudolph, Wolfram W; Irmer, Gert

    2015-01-01

    Raman spectra of aqueous lanthanum perchlorate, triflate (trifluorosulfonate), chloride and nitrate solutions were measured over a broad concentration (0.121-3.050 mol L(-1)) range at room temperature (23 °C). A very weak mode at 343 cm(-1) with a full width at half height at 49 cm(-1) in the isotropic spectrum suggests that the nona-aqua La(III) ion is thermodynamically stable in dilute perchlorate solutions (∼0.2 mol L(-1)) while in concentrated perchlorate solutions outer-sphere ion pairs and contact ion pairs are formed. The La(3+) nona-hydrate was also detected in a 1.2 mol L(-1) La(CF3SO3)3(aq). In lanthanum chloride solutions chloro-complex formation was detected over the measured concentration range from 0.5-3.050 mol L(-1). The chloro-complexes in LaCl3(aq) are fairly weak and disappear with dilution. At a concentration complexes disappeared. In LaCl3 solutions, with additional HCl, a series of chloro-complexes of the type [La(OH2)(9-n)Cln](+3-n) (n = 1-3) were formed. The La(NO3)3(aq) spectra were compared with a spectrum of a 0.409 mol L(-1) NaNO3(aq) and it was concluded that in La(NO3)3(aq) over the concentration range from 0.121-1.844 mol L(-1), nitrato-complexes, [La(OH2)(9-n)(NO3)n](+3-n) (n = 1, 2) were formed. These nitrato-complexes are quite weak and disappear with dilution La(OH2)9](3+) with the polarizable dielectric continuum are in good agreement with data from recent structural experimental measurements and high quality simulations. The DFT frequency of the La-O stretching mode at 328.2 cm(-1), is only slightly smaller than the experimental one.

  3. Propiedades de Superficie en Soluciones Acuosas Diluidas de Alcoholes con Tres Carbonos Surface Properties of Aqueous Dilute Solutions of Alcohols with Three Carbons

    Directory of Open Access Journals (Sweden)

    Manuel S Páez

    2009-01-01

    Full Text Available Se determinó la tensión superficial de soluciones acuosas diluidas de alcoholes mono y polihidroxílicos a varias temperaturas usando el método de ascenso capilar. Los datos experimentales fueron usados para evaluar la entropía, la entalpía y la concentración superficial, la constante de enlazamiento y la pendiente límite. Se analizan el efecto de la temperatura, del tamaño de la cadena alquílica y de la posición de los grupos hidroxilos en el soluto expuestos al solvente. Los resultados muestran que la tensión superficial de las soluciones varía linealmente con la temperatura y que el carácter hidrofóbico de estos solutos, aumenta según el orden: 123PT, 13PD, 12PD y 1P. Adicionalmente se detectaron procesos de rompimiento de enlaces de las esferas de hidratación (entalpías positivas y aumento del desorden molecular (entropías positivas, en la región superficial.Surface tension of diluted aqueous solutions of mono and polyhydroxilic alcohols was determined at various temperatures using the method of capillary rising. The experimental data were used to evaluate surface entropies, enthalpies, and concentration, binding constants and the limiting slope. The effect of temperature, of the alkyl chain size and of the position of the hydroxyl groups in the solute that were exposed to the solvent are analyzed. The results show that the surface tension of the solutions varies lineally with the temperature and that the hydrophobic character of these solutes rises according to the order: 123PT, 13PD, 12PD y 1P. Additionally, bond breaking processes of the hydration spheres (positive enthalpies and molecular disorder increase (positive entropies in the surface region were detected.

  4. Salt dependent stability of stearic acid Langmuir-Blodgett films exposed to aqueous electrolytes.

    Science.gov (United States)

    Kumar, Naveen; Wang, Lei; Siretanu, Igor; Duits, Michel; Mugele, Frieder

    2013-04-30

    We use contact angle goniometry, imaging ellipsometry, and atomic force microscopy to study the stability and wettability of Langmuir-Blodgett (LB) monolayers of stearic acid on silica substrates, upon drying and exposure to aqueous solutions of varying salinity. The influences of Ca(2+) and Na(+) ions are compared by varying their concentrations, both in the subphase before the LB transfer, and in the droplets to which the dried LB layers are exposed. Ca(2+) ions in the subphase are found to enhance the stability, leading to contact angles up to 100°, as compared to less than 5° for Na(+). Consistent with the macroscopic wettability, AFM images show almost intact films with few holes exposing bare substrate when prepared in the presence of Ca(2+), while subphases containing Na(+) result in large areas of bare substrate after exposure to aqueous drops. The observations on varying the composition of the droplets corroborate the stabilizing effect of Ca(2+). We attribute these findings to the cation-bridging ability of Ca(2+) ions, which can bind the negatively charged stearate groups to the negatively charged substrates. We discuss the relevance of our findings in the context of enhanced oil recovery.

  5. 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

    The static permittivity is the most important physical property for thermodynamic models that account for the electrostatic interactions between ions. The measured static permittivity in mixtures containing electrolytes is reduced due to kinetic depolarization and reorientation of the dipoles...... 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...... to associating mixtures. Wertheim’s association model as formulated in the statistical associating fluid theory is used to account for hydrogen-bonding molecules and ion–solvent association. Finally, we compare the Debye–Hückel Helmholtz energy obtained using an empirical model with the new physical model...

  6. Influence of pH, temperature, and concentration on stabilization of aqueous hornet silk solution and fabrication of salt-free materials.

    Science.gov (United States)

    Kameda, Tsunenori

    2015-01-01

    We found that an aqueous solution of silk from cocoons produced by hornet larvae (hornet silk) can be obtained when the solution is adjusted to basic conditions of pH > 9.2. It is known that native hornet cocoons can be dissolved in concentrated aqueous solution of salts, such as lithium bromide (LiBr) and calcium chloride (CaCl2). Upon the removal of these salts from solution by dialysis, solidification, gelation, or sedimentation of hornet silk is known to occur. In the present study, under basic conditions, however, no such solidification occurred, even after salt removal. In this study, ammonia was used for alkalization of solution because it is volatilized during the casting process and pure hornet silk materials can be obtained after drying. The effects of the concentrations of hornet silk and ammonia, as well as dialysis temperature, on preventing gelation during dialysis were investigated. Dialysis conditions that limit the degradation of hornet silk by hydrolysis in alkali solution were identified. Moreover, casting conditions to prepare flexible and transparent hornet silk film from aqueous ammonia solution were optimized. Molecular structural analysis of hornet silk in aqueous ammonia solution and cast film indicated the formation of α-helix conformations.

  7. 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,...

  8. 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.

  9. Bupivacaine salts of diflunisal and other aromatic hydroxycarboxylic acids: aqueous solubility and release characteristics from solutions and suspensions using a rotating dialysis cell model.

    Science.gov (United States)

    Østergaard, Jesper; Larsen, Susan W; Parshad, Henrik; Larsen, Claus

    2005-11-01

    In the search for poorly soluble bupivacaine salts potentially enabling prolonged postoperative pain relief after local joint administration in the form of suspensions the solubility of bupivacaine salts of diflunisal and other aromatic hydroxycarboxylic acids were investigated together with the release characteristics of selected 1:1 salts from solutions and suspensions using a rotating dialysis cell model. The poorest soluble bupivacaine salts were obtained from the aromatic ortho-hydroxycarboxylic acids diflunisal, 5-iodosalicylic acid, and salicylic acid (aqueous solubilities: 0.6-1.9 mM at 37 degrees C). Diffusant appearance rates in the acceptor phase upon instillation of solutions of various salts in the donor cell applied to first-order kinetics. Calculated permeability coefficients for bupivacaine and the counterions diflunisal, 5-iodosalicylic acid, and mandelic acid were found to be correlated with the molecular size of the diffusants. Release experiments at physiological pH involving suspensions of the bupivacaine-diflunisal salt revealed that at each sampling point the diflunisal concentration exceeded that of bupivacaine in the acceptor phase. However, after an initial lag period, a steady state situation was attained resulting in equal and constant fluxes of the two diffusants controlled by the permeability coefficients in combination with the solubility product of the salt. Due to the fact that the saturation solubility of the bupivacaine-salicylic acid salt in water exceeded that of bupivacaine at pH 7.4, suspensions of the latter salt were unable to provide simultaneous release of the cationic and anionic species at pH 7.4. The release profiles were characterised by a rapid release of salicylate accompanied by a much slower appearance of bupivacaine in the acceptor phase caused by precipitation of bupivacaine base from the solution upon dissolution of the salt in the donor cell.

  10. Cellulose aerogels prepared from an aqueous zinc chloride salt hydrate melt.

    Science.gov (United States)

    Schestakow, Maria; Karadagli, Ilknur; Ratke, Lorenz

    2016-02-10

    Monolithic cellulose aerogels are prepared using a salt hydrate melt based on cheap zinc chloride tetrahydrate (ZnCl2·4H2O) that can be washed out of the wet gel-body by using common solvents such as water, ethanol, isopropanol or acetone. Cellulose aerogels with concentrations of 1-5 wt.% cellulose were produced. These aerogels are characterized with respect to shrinkage, density and surface area as well as mechanical properties and micro-structure via SEM. Cellulose aerogels regenerated in acetone show a specific surface area of around 340 m(2)g(-1) being 60% higher than those regenerated in water. The onset of irreversible plastic deformation under compressive load is around 0.8 MPa for acetone-regenerated aerogels and thus a factor of two larger compared to ethanol regenerated ones. The Young's modulus depends almost linearly on the cellulose concentration which is observed for all regenerative fluids with the exception of water. The results achieved are presented in light of the polarity and ability of solvation of ZnCl2·4H2O in the regenerative fluids used.

  11. 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.

  12. Assessment of the combined approach of N-alkylation and salt formation to enhance aqueous solubility of tertiary amines using bupivacaine as a model drug

    DEFF Research Database (Denmark)

    Nielsen, Anders Bach; Frydenvang, Karla Andrea; Liljefors, Tommy;

    2005-01-01

    Quaternary prodrug types of poorly water-soluble tertiary amines have been shown to exhibit significantly enhanced solubilities as compared to the parent amine. In the present study the combined effect of N-alkylation and salt formation to enhance aqueous solubility of tertiary amines have been...... tertiary amine (up to a factor of 3200 at pH 8). A moderate reduction in solubility with increasing length of the alkyl chain was observed for the iodide salts of the N-alkylated bupivacaine derivatives. In case of the N-methyl-bupivacaine derivative variation of the counterion had a significant impact...

  13. Influence of the temperature and type of salt on the phase equilibrium of peg 1500 + potassium phosphate and peg 1500 + sodium citrate aqueous two-phase systems

    Directory of Open Access Journals (Sweden)

    Carolina P. Carvalho

    2008-01-01

    Full Text Available The present work analyzed the effect of the temperature and type of salt on the phase equilibrium of aqueous two-phase systems (ATPS formed by poly (ethylene glycol (PEG 1500 + potassium phosphate, from (278.15 to 318.15 K, and PEG 1500 + sodium citrate, from (278.15 to 298.15 K. The rise of the temperature normally increased the slope of the tie line (STL. With respect to the influence of the type of salt, sodium citrate showed better capability to induce phase separation, when compared to potassium phosphate.

  14. Co-precipitation in aqueous solution synthesis of magnetite nanoparticles using iron(III salts as precursors

    Directory of Open Access Journals (Sweden)

    Mutasim I. Khalil

    2015-03-01

    Full Text Available An innovative quantitative synthetic method for preparing magnetite nanoparticles was achieved by co-precipitation in aqueous solution using only one single iron(III salt as a precursor. A 2 Fe(III:1 Fe(II mole ratio was first attained in solution by reducing iron(III using KI solution, followed by filtering the iodine formed and hydrolyzing the filtrate by 25% ammonium hydroxide solution at pH 9–11. A high selectivity and atom economy percents were achieved indicating that the method is environmentally benign and green. The as-synthesized nanoparticles were characterized by fourier transform infrared spectroscopy (FTIR, X-ray diffraction (XRD, field emission scanning electron microscopy (FESEM, field emission transmission electron microscopy (FETEM, selected area electron diffraction (SAED, and 57Fe Mössbauer spectroscopy. Magnetite nanocrystals (d: 7.84 ± 0.05 nm and nanorods (d: 6.3 ± 0.2 nm; l: 46.2 ± 0.9 formation was evident.

  15. Extraction and purification of wheat-esterase using aqueous two-phase systems of ionic liquid and salt.

    Science.gov (United States)

    Jiang, Bin; Feng, Zhibiao; Liu, Chunhong; Xu, Yingcao; Li, Dongmei; Ji, Guo

    2015-05-01

    To explore a new and simple rapid extraction and purification technique for wheat-esterase, an ionic liquids (ILs)-based aqueous two-phase system (ATPS) was developed for the purification of wheat-esterase from wheat extracts. Effects of various process parameters such as the concentrations of [Bmim]BF4, the types and concentrations of phase-forming salt, the system pH and the temperature on partitioning of wheat-esterase were evaluated. The obtained data indicated that wheat-esterase was preferentially partitioned into the ILs-rich phase and the ATPS composed of 20 % [Bmim]BF4 (w/w) and 25 % (w/w) NaH2PO4(pH = 4.8) showed good selectivity on wheat-esterase. Under the optimum conditions, wheat-esterase was purified with an acceptable yield (88.93 %), but produced wheat-esterase was 4.23 times as pure. It was obvious that temperature shows little influence on the purification between 10 and 50 °C. Sephadex G-150FF revealed that the band intensity of contaminating proteins in ATPS fraction almost disappeared. Therefore, ILs-based ATPS was an effective method for partitioning and recovery of wheat-esterase from wheat crude extracts.

  16. Inclusion of mPRISM potential for polymer-induced protein interactions enables modeling of second osmotic virial coefficients in aqueous polymer-salt solutions.

    Science.gov (United States)

    Herhut, Marcel; Brandenbusch, Christoph; Sadowski, Gabriele

    2016-01-01

    The downstream processing of therapeutic proteins is a challenging task. Key information needed to estimate applicable workup strategies (e.g. crystallization) are the interactions of the proteins with other components in solution. This information can be deduced from the second osmotic virial coefficient B22 , measurable by static light scattering. Thermodynamic models are very valuable for predicting B22 data for different process conditions and thus decrease the experimental effort. Available B22 models consider aqueous salt solutions but fail for the prediction of B22 if an additional polymer is present in solution. This is due to the fact that depending on the polymer concentration protein-protein interactions are not rectified as assumed within these models. In this work, we developed an extension of the xDLVO model to predict B22 data of proteins in aqueous polymer-salt solutions. To show the broad applicability of the model, lysozyme, γ-globulin and D-xylose ketol isomerase in aqueous salt solution containing polyethylene glycol were considered. For all proteins considered, the modified xDLVO model was able to predict the experimentally observed non-monotonical course in B22 data with high accuracy. When used in an early stage in process development, the model will contribute to an efficient and cost effective downstream processing development.

  17. Extended UNIQUAC model for correlation and prediction of vapour-liquid-solid equilibria in aqueous salt systems containing non-electrolytes

    DEFF Research Database (Denmark)

    Iliuta, Maria C.; Thomsen, Kaj; Rasmussen, Peter

    2000-01-01

    . The calculations are based on an extensive database consisting of salt solubility data in pure and mixed solvents, VLE data for solvent mixtures and mixed solvent-electrolyte systems and thermal properties for mixed solvent solutions. Application of the model to the methanol-water system in the presence of several...... to aqueous salt systems containing non-electrolytes in order to demonstrate its ability in representing solid-liquid-vapour (SLV) equilibrium and thermal property data for these strongly non-ideal systems. The model requires only pure component and binary temperature-dependent interaction parameters...... behaviour of methanol-water-three salts systems is illustrated. (C) 2000 Elsevier Science Ltd. All rights reserved....

  18. 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...

  19. Development of counter current salting-out homogenous liquid-liquid extraction for isolation and preconcentration of some pesticides from aqueous samples.

    Science.gov (United States)

    Farajzadeh, Mir Ali; Feriduni, Behruz; Afshar Mogaddam, Mohammad Reza

    2015-07-23

    In this paper, a new version of salting-out homogenous liquid-liquid extraction based on counter current mode combined with dispersive liquid-liquid microextraction has been developed for the extraction and preconcentration of some pesticides from aqueous samples and their determination by gas chromatography-flame ionization detection. In order to perform the method, aqueous solution of the analytes containing acetonitrile and 1,2-dibromoethane is transferred into a narrow bore tube which is filled partially with NaCl. During passing the solution through the tube, fine droplets of the organic phase are produced at the interface of solution and salt which go up through the tube and form a separated layer on the aqueous phase. The collected organic phase is removed and injected into de-ionized water for more enrichment of the analytes. Under the optimum extraction conditions, the method shows broad linear ranges for the target analytes. Enrichment factors and limits of detection for the selected pesticides are obtained in the ranges of 3480-3800 and 0.1-5μgL(-1), respectively. Relative standard deviations are in the range of 2-7% (n=6, C=50 or 100μgL(-1), each analyte). Finally, some aqueous samples were successfully analyzed using the developed method.

  20. Ultrasonic-assisted synthesis of aqueous CdTe/CdS QDs in salt water bath heating

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Yinglian [College of Food Science and Engineering, Ocean University of China, Qingdao 266003, Shandong Province (China); College of Food Science and Engineering, Qingdao Agricultural University of China, Qingdao 266109, Shandong Province (China); Li, Chunsheng; Xu, Ying [College of Food Science and Engineering, Ocean University of China, Qingdao 266003, Shandong Province (China); Wang, Dongfeng, E-mail: wangdf@ouc.edu.cn [College of Food Science and Engineering, Ocean University of China, Qingdao 266003, Shandong Province (China)

    2014-09-01

    Highlights: • Ultrasonic promotes formation of crystal nucleus and QDs were synthesized in 0.5 h. • The new heating method provides a PLQY of up to 97.13%. • The synthesis mechanism of the core shell structure of the CdTe/CdS QDs was inferred. • The preparation method was efficient, simple and clean. - Abstract: A novel simple method for fast and efficient synthesis of aqueous CdTe/CdS quantum dots (QDs) with core–shell structure was developed by using salt water bath heating with the ultrasonic-assisted technique in this paper. The formation of crystal nucleus was promoted by ultrasonic and CdTe/CdS QDs with blue fluorescence were synthesized only in 0.5 h. The heat source was bath heating in salt water solution at 60% NaCl and the heating temperature could reach 105 °C. The heating method solved the biggest drawback of low photoluminescence quantum yield (PLQY) of ordinal bath heating in water. The preparation was cheap, simple and had less pollution to the environment. The properties of the CdTe/CdS QDs were thoroughly investigated by ultraviolet–visible (UV–vis), photoluminescence (PL), transmission electron microscope (TEM), laser size analysis, fourier transform infrared spectra (FTIR), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). Different CdTe/CdS QDs with core shell structure were efficiently synthesized and the maximum PLQY could reach 97.13% when refluxing at 105 °C for 2 h. These QDs exhibited uniform dispersity, high fluorescence intensity, good optical property and long life of fluorescent. The synthesis mechanism of the core shell structure of the QDs was inferred that the Cd{sup 2+} might coordinate with sulfur (S) as well as thiol propionate (–SCH{sub 2}CH{sub 2}COO{sup −1}) to constitute two relatively thick compound layers on the QDs surface as passive shells.

  1. PDMS渗透蒸发膜分离稀水溶液中苯的模型研究%Modeling of Pervaporation Separation Benzene from Dilute Aqueous Solutions Through Polydimethylsiloxane Membranes

    Institute of Scientific and Technical Information of China (English)

    彭福兵; 姜忠义

    2005-01-01

    A modified solution-diffusion model was established based on Flory-Huggins thermodynamic theory and Fujita's free volume theory. This model was used for description of the mass transfer of removal benzene from dilute aqueous solutions through polydimethylsiloxane (PDMS) membranes. The effect of component concentration on the interaction parameter between components, that of the polymer membrane on the selectivity to benzene, and that of feed concentration and temperature on the permeation flux and separation factor of benzene/water through PDMS membranes were investigated. Calculated pervaporation fluxes of benzene and water were compared with the experimental results and were in good agreement with the experimental data.

  2. 利用DMO-M离子交换树脂除去稀溶液中的汞%Removal of Mercury from Dilute Aqueous Solution Using Mercaptoacetimide of Aminophenol Resin Duolite A-7

    Institute of Scientific and Technical Information of China (English)

    C.S.Zhu(朱长生); Z.K.Duan(段正康); Z.S.Liu; G.L.Rempel

    2004-01-01

    A mercaptan - containing resin, DMO- M, with high redox capacity- 6.00 mequiv / g, prepared by reacting mercaptoacetyl chloride with the aminophenol resin Duolite A-7 in free-base form has been used to remove mercury in dilute aqueous solution. The resin has high mercury removal capacity; 1200mg/g. Sodium chloride affects the equilibrium sorption of mercury on the resin. At lower pH values, below 1.76, mercury sorption of the resin was greatly reduced. The sorbed mercury is partially removed by 2 mol/L HCl solution containing 5 % thiourea.

  3. Electrochemical synthesis of nanocrystalline In2O3:Sn (ITO) in an aqueous system with ammonium acetate as conducting salt.

    Science.gov (United States)

    Veith, M; Rabung, B; Grobelsek, I; Klook, M; Wagner, F E; Quilitz, M

    2009-04-01

    Nanoscaled so called indium tin oxide In2O3:Sn (ITO) with a specific BET surface area of 50 m2/g to 60 m2/g was prepared via an electrochemical method in an aqueous system containing ammonium acetate as conductive salt. As an intermediate product of the synthesis nanocrystalline In(OH)3 is obtained which serves as a precursor for the subsequent calcinations accompanied by tin doping resulting in ITO powders with various tin concentrations. Its phase transitions and the reduction behaviour of hydroxide to oxide during the calcination process in air flow and forming gas atmosphere of N2 to H2 ratio of 95 to 5 respectively, have been investigated by high temperature X-ray diffraction, TG/DSC/MS, HRTEM and SEM analysis. Depending on the atmosphere dehydration of tin doped In(OH)3 started at 150 degrees C, cubic ITO solid solution formed between 190 degrees C and 300 degrees C. The total weight loss of the hydroxide of approx. 21% occurred mainly below 360 degrees C and the burn-out of organic components mainly between 308 degrees C and 316 degrees C. The results of DSC and MS analyses were in good agreement with the results of the X-ray diffraction. In addition, the products have been characterized by EDX associated with TEM, XPS, ICP-AES, BET analysis and 119Sn Mössbauer spectroscopy. Completely reacted samples of ITO have been processed to pellets, calcined and sintered in the temperature range between 900 degrees C and 1100 degrees C and characterized by measurements of the electrical conductivities of bulk and surface in the reduced as well as in the oxidized state giving values up to 1400 Scm(-1).

  4. Effects of salt concentrations of the aqueous peptide-amphiphile solutions on the sol-gel transitions, the gelation speed, and the gel characteristics.

    Science.gov (United States)

    Otsuka, Takahiro; Maeda, Tomoki; Hotta, Atsushi

    2014-10-02

    Hydrogels made of peptide amphiphiles (PA) have attracted a lot of interest in biomedical fields. Considering the applications of PA hydrogels, the control of the gelation speed and the gel characteristics is essential to predominantly determine the usefulness and practicability of the hydrogels. In this work, the effects of the salt concentrations using sodium dihydrogenorthophosphate (NaH2PO4) on the sol-gel transition behaviors, especially the gelation speed and the gel characteristics of the designed PA (C16-W3K) hydrogels in aqueous solution were discussed. It was found that the original solution state before rheological testing was independent of the salt concentration, which was confirmed by observing the self-assembly structures and the peptide secondary structures of PA through transmission electron microscopy (TEM) and circular dichroism spectroscopy (CD). The PA solutions with different salt concentrations, however, presented a profound difference in the gelation speed and the gel characteristics: the solution exhibited higher gelation speeds and higher mechanical properties at higher salt concentrations. Concurrently, the density, the length of wormlike micelles, and the conformational ratio of β-sheets to α-helices in the equilibrium PA solutions all increased with the increase in the salt concentrations.

  5. Partition behavior of surfactants, butanol, and salt during application of density-modified displacement of dense non-aqueous phase liquids

    Energy Technology Data Exchange (ETDEWEB)

    Damrongsiri, S. [Center of Excellence on Hazardous Substance Management (HSM), Chulalongkorn University, Phaya-Thai Rd., Bangkok (Thailand); Tongcumpou, C., E-mail: tchantra@chula.ac.th [Center of Excellence on Hazardous Substance Management (HSM), Chulalongkorn University, Phaya-Thai Rd., Bangkok (Thailand); Environmental Research Institute, Chulalongkorn University (Thailand); Sabatini, D.A. [School of Civil Engineering and Environmental Science, The University of Oklahoma, Oklahoma (United States)

    2013-03-15

    Highlights: ► Aqueous surfactant increases the partition of butanol aqueous phase. ► Water partition to NAPL phase via butanol and surfactant in NAPL phase. ► PCE partition to aqueous phase by solubilization into micelles. ► Surfactants cause the dramatically partition of water to NAPL phase. ► Aqueous salt dispels surfactant to NAPL phase. -- Abstract: Density-modified displacement (DMD) is a recent approach for removal of trapped dense NAPL (DNAPL). In this study, butanol and surfactant are contacted with the DNAPL to both reduce the density as well as release the trapped DNAPL (perchloroethylene: PCE). The objective of the study was to determine the distribution of each component (e.g., butanol, surfactant, water, PCE) between the original aqueous and PCE phases during the application of DMD. The results indicated that the presence of the surfactant increased the amount of n-butanol required to make the NAPL phase reach its desired density. In addition, water and anionic surfactant were found to partition along with the BuOH into the PCE phase. The water also found partitioned to reverse micelles in the modified phase. Addition of salt was seen to increase partitioning of surfactant to BuOH containing PCE phase. Subsequently, a large amount of water was solubilized into reverse micelles which lead to significantly increase in volume of the PCE phase. This work thus demonstrates the role of each component and the implications for the operation design of an aquifer treatment using the DMD technique.

  6. 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

  7. Integrated method of thermosensitive triblock copolymer-salt aqueous two phase extraction and dialysis membrane separation for purification of lycium barbarum polysaccharide.

    Science.gov (United States)

    Wang, Yun; Hu, Xiaowei; Han, Juan; Ni, Liang; Tang, Xu; Hu, Yutao; Chen, Tong

    2016-03-01

    A polymer-salt aqueous two-phase system (ATPS) consisting of thermosensitive copolymer ethylene-oxide-b-propylene-oxide-b-ethylene-oxide (EOPOEO) and NaH2PO4 was employed in deproteinization for lycium barbarum polysaccharide (LBP). The effects of salt type and concentration, EOPOEO concentration, amount of crude LBP solution and temperature were studied. In the primary extraction process, LBP was preferentially partitioned to the bottom (salt-rich) phase with high recovery ratio of 96.3%, while 94.4% of impurity protein was removed to the top (EOPOEO-rich) phase. Moreover, the majority of pigments could be discarded to top phase. After phase-separation, the LBP in the bottom phase was further purified by dialysis membrane to remove salt and other small molecular impurities. The purity of LBP was enhanced to 64%. Additionally, the FT-IR spectrum was used to identify LBP. EOPOEO was recovered by a temperature-induced separation, and reused in a new ATPS. An ideal extraction and recycle result were achieved.

  8. Polarity, selectivity and performance of hydrophilic organic/salt-containing aqueous two-phase system on counter-current chromatography for polar compounds.

    Science.gov (United States)

    Liu, Dan; Hong, Zhilai; Gao, Mingzhe; Wang, Zhixin; Gu, Ming; Zhang, Xiaozhe; Xiao, Hongbin

    2016-05-27

    The essential attributes of a solvent system for separation polar compounds on CCC are polarity, selectively and performance. Here, hydrophilic organic/salt-containing aqueous two-phase system (HO/S TPS) was evaluated as an alternative solvent system for CCC separation of polar compounds. Polarity measurements based on Rohrschneider-Snyder parameter was developed as quantitative assessing the polarity of HO/S TPS and comparing with an organic/aqueous system. All investigated 1-butanol/ethanol/saturated ammonium sulfate solution/water (BEAsWat) and 1-butanol/ethanol/saturated dipotassium hydrogen phosphate solution/water (BEDhpWat) systems with polarity values of organic phase from 4.5 to 6.8, were more polar than chloroform/methanol/water (1/1/1). The considerable water content of BEAsWat and BEDhpWat (0/1/1/1/) was 45.4 and 42.6% (w%) of hydrophilic organic phase, and 66.4 and 51.2% (w%) of salt-containing aqueous phase, respectively, closed to conventional aqueous two-phase system. Therefore, the polarity of HO/S TPS is in the middle of organic/aqueous and aqueous two-phase system. The LogKC values of twenty four polar compounds as model mixture confirmed that the polarities of HO/S TPSs were matched to that of the polar compounds and shown to be a very selective technique capable of separating positional isomers. Moreover, BEAsWat and BEDhpWat systems can be easily retained in CCC column with suitable elution mode. The hydrodynamic behavior reversion of HO/S TPS on hydrodynamic CCC was observed and was tentatively explained based on the density difference. Finally, caffeoylquinic acid isomers and dihydroxybenzoic acid isomers were successfully separated with HO/S TPS on CCC, respectively. Those results demonstrate that HO/S TPS on CCC is a performant and stable way to separate polar compounds from natural products.

  9. Secondary Organic Aerosol and Brown Carbon Formation in the Sunlit Aqueous Phase: Aldehyde Photooxidation in the Presence of Ammonium Salts and Amines

    Science.gov (United States)

    De Haan, D. O.; Galloway, M. M.; Sharp, K. D.; Jiménez, N. G.

    2014-12-01

    The chemistry of water-soluble carbonyl compounds in clouds is now acknowledged as an important source of secondary organic aerosol. These reactive carbonyl compounds are oxidized to carboxylic acids and form oligomers by radical-radical reactions and by "dark reactions" with ammonium salts (AS) and/or amines. The latter class of reactions also produces light-absorbing brown carbon compounds, especially reactions involving methylglyoxal or glyoxal and amines. However, recent work has found that UV light fades the color of glyoxal + AS and methylgyloxal + AS reaction mixtures. We recently studied aldehyde-AS-amine reactions in sunlight and in control vessels at the same temperature to determine the effects of solar radiation on the aqueous-phase production of brown carbon. In sunlight, methylglyoxal reaction mixtures lost their initial color and failed to brown, indicating the photolytic loss of reactants and/or pre-brown intermediates. In many other reactions, brown products are lost to photolysis, reducing the overall browning of solutions exposed to sunlight. In other experiments, hydrogen peroxide was added to generate OH radicals by photolysis. In the presence of OH radicals, some carbonyl compound mixtures (e.g. those containing hydroxyacetone or glycolaldehyde) browned more rapidly when exposed to sunlight. This indicates the existence of uncharacterized photooxidative browning pathways involving aqueous-phase OH radicals, carbonyls, ammonium salts, and/or amine compounds.

  10. 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)

    CERN Document Server

    Bian, Hong-tao; 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 salts caused increase of the thickness of the interfacial water layer at the surfaces to a certain extent. Noticeably, both the cations and the anions contributed to the changes, and the abilities to increase the thickness of the interfacial water layer were in the following order: KBr > NaBr > KCl > NaCl ~ NaF > KF. Since these changes can not be factorized into individual anion and cation contributions, there are possible ion pairing or association effects, especially for the NaF case. We also found that the orientational ...

  11. Excellent dynamic stability under saturated salt solution for aqueous quantum dots capped by multi-branched ligands

    Science.gov (United States)

    Xu, Jingkun; Xu, Shuhong; Lv, Changgui; Wang, Chunlei; Cui, Yiping

    2016-09-01

    Preparing quantum dots (QDs) with strong stability against salts is extremely important in some environments with ultrahigh salts concentration, such as the oil exploitation, wastewater treatment and biological markers. In this paper, we reported a simple new method to prepared highly stable QDs by using multi-branched ligands. Our results suggested that multi-branched ligands-capped QDs have extremely good dynamic stability even in salt-saturated solution. Unlike to traditional dynamic stability theory, which considers the electrostatic repulsion of QDs dominant QD stability, the current work found a new determined factor: the steric hindrance of ligand structure. The high steric hindrance effect of multi-branched ligands can maintain the single dispersity of QDs even at extremely low electrostatic repulsion. As a result, QDs with ultrahigh stability against salts can be realized.

  12. Palladium-catalyzed heck coupling reaction of aryl bromides in aqueous media using tetrahydropyrimidinium salts as carbene ligands.

    Science.gov (United States)

    Yaşar, Sedat; Ozcan, Emine Ozge; Gürbüz, Nevin; Cetinkaya, Bekir; Ozdemir, Ismail

    2010-01-28

    An efficient and stereoselective catalytic system for the Heck cross coupling reaction using novel 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (1, LHX) and Pd(OAc)2 loading has been reported. The palladium complexes derived from the salts 1a-f prepared in situ exhibit good catalytic activity in the Heck coupling reaction of aryl bromides under mild conditions.

  13. Palladium-Catalyzed Heck Coupling Reaction of Aryl Bromides in Aqueous Media Using Tetrahydropyrimidinium Salts as Carbene Ligands

    Directory of Open Access Journals (Sweden)

    İsmail Özdemir

    2010-01-01

    Full Text Available An efficient and stereoselective catalytic system for the Heck cross coupling reaction using novel 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (1, LHX and Pd(OAc2 loading has been reported. The palladium complexes derived from the salts 1a-f prepared in situ exhibit good catalytic activity in the Heck coupling reaction of aryl bromides under mild conditions.

  14. UV-visible Absorption Study of the Self-association of Non-ionic Chromonic Triphenylenes TP6EOnM (n = 2, 3, 4) in Dilute Aqueous Solutions: Impact of Chain Length on Aggregation.

    Science.gov (United States)

    Herbaut, Antoine; Baranoff, Etienne

    2015-01-01

    A series of triphenylenes with oligoethoxy chains of various length, TP6EOnM with n = 2, 3, 4, has been synthesised and purified by HPLC. The self-association of these disc-shaped molecules in dilute aqueous solutions (∼10(-7) to ∼4 × 10(-4) M) has been studied by UV-visible absorption spectroscopy. The free energy of association decreases as the length of the chains increases. As a result, for a given concentration, the average size of aggregate diminishes as the chain length increases. While the absorption properties of the monomer are identical for the three molecules, the extinction coefficients of solutions of the three triphenylenes at a given concentration are significantly different and are directly linked to the average size of the aggregates. The change of epsilon values upon aggregation could explain the trend generally observed with dyes for solar cells substituted with chains of increasing length showing increasing extinction coefficient values.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1995-10-01

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

  16. Molecular Dynamics Simulation of Surface Tension of NaCl Aqueous Solution at 298.15K: from Diluted to Highly Supersaturated Concentrations

    Science.gov (United States)

    Wang, Xiaoxiang; Chen, Chuchu; Poeschl, Ulirch; Su, Hang; Cheng, Yafang

    2017-04-01

    Sodium chloride (NaCl) is one of the key components of atmospheric aerosol particles. Concentration-depend surface tension of aqueous NaCl solution is essential to determine the equilibrium between droplet NaCl solution and water vapor, which is important in regards to aerosol-cloud interaction and aerosol climate effects. Although supersaturated NaCl droplets can be widely found under atmospheric conditions, the experimental determined concentration dependency of surface tension is limited up to the saturated concentration range due to technical difficulties, i.e., heterogeneous nucleation since nearly all surface tension measurement techniques requires contact of the sensor and solution surface. In this study, the surface tension of NaCl aqueous solution with solute mass fraction from 0 to 1 was calculated using molecular dynamics (MD) simulation. The surface tension increases monotonically and near linearly when mass fraction of NaCl (xNaCl) is lower than 0.265 (saturation point), which follows theoretical predictions (e.g., E-AIM, SP parameterization, and PK parameterization). Once entering into the supersaturated concentration range, the calculated surface tension starts to deviate from the near-linear extrapolation and adopts a slightly higher increasing rate until xNaCl of 0.35. We found that these two increasing phases (xNaCl 0.35) is mainly driven by the increase of excessive surface enthalpy when the solution becomes concentrated. After that, the surface tension remains almost unchanged until xNaCl of 0.52. This phenomenon is supported by the results from experiment based Differential Koehler Analyses. The stable surface tension in this concentration range is attributed to a simultaneous change of surface excess enthalpy and entropy at similar degree. When the NaCl solution is getting more concentrated than xNaCl of 0.52, the simulated surface tension regains an even faster growing momentum and shows the tendency of ultimately approaching the surface

  17. 黄芩甙在EOPO/盐双水相系统中的分配系数测定及关联%Measurement and Correlation of Partition Coefficients of Baicalin in EOPO/Salt Aqueous Two-Phase Systems

    Institute of Scientific and Technical Information of China (English)

    李伟; 朱自强

    2002-01-01

    The partition coefficients of baicalin were measured in ethylene oxide and propylene oxide (EOPO)/salt aqueous two-phase systemsat 298.15K. It was found that most of baicalin partitioned into EOPO-rich phase. The partition coefficients of baicalin varied from 10 to 120.The effect of various factors, including tie-line length, salt composition, molecular weight of EOPO, and solution pH, on the partition behaviorwas investigated in EOPO/salt systems. Furthermore the partition coefficients of baicalin were correlated using the modified Diamond-Hsumodel. Good agreement with experimental data is obtained. The average relative deviations are less than 5.0%.

  18. Data on energy-band-gap characteristics of composite nanoparticles obtained by modification of the amorphous potassium polytitanate in aqueous solutions of transition metal salts

    Directory of Open Access Journals (Sweden)

    D.A. Zimnyakov

    2016-06-01

    Full Text Available Here we present the data on the energy-band-gap characteristics of composite nanoparticles produced by modification of the amorphous potassium polytitanate in aqueous solutions of different transition metal salts. Band gap characteristics are investigated using diffuse reflection spectra of the obtained powders. Calculated logarithmic derivative quantity of the Kubelka–Munk function reveals a presence of local maxima in the regions 0.5–1.5 eV and 1.6–3.0 eV which correspond to band gap values of the investigated materials. The values might be related to the constituents of the composite nanoparticles and intermediate products of their chemical interaction.

  19. Effects of Na2SO4 or NaCl on sonochemical degradation of phenolic compounds in an aqueous solution under Ar: Positive and negative effects induced by the presence of salts.

    Science.gov (United States)

    Uddin, Md Helal; Nanzai, Ben; Okitsu, Kenji

    2016-01-01

    Sonochemical degradation of 4-chlorophenol, phenol, catechol and resorcinol was studied under Ar at 200 kHz in the absence and presence of Na2SO4 or NaCl. The rates of sonochemical degradation in the absence of salts decreased in the order 4-chlorophenol>phenol>catechol>resorcinol and this order was in good agreement with the order of log P (partition coefficient) value of each phenolic compound. The effects of salts on the rates of sonochemical degradation consisted of no effect or slight negative or positive effects. We discussed these unclear results based on two viewpoints: one was based on the changes in pseudo hydrophobicity and/or diffusion behavior of phenolic compounds and the other was based on the changes in solubility of Ar gas. The measured log P value of each phenolic compound slightly increased with increasing salt concentration. In addition, the dynamic surface tension for 4-chlorophenol aqueous solution in the absence and presence of Na2SO4 or NaCl suggested that phenolic compounds more easily accumulated at the interface region of bubbles at higher salt concentration. These results indicated that the rates of sonochemical degradation should be enhanced by the addition of salts. On the other hand, the calculated Ar gas solubility was confirmed to decrease with increasing salt concentration. The yield of H2O2 formed in the presence of Na2SO4 or NaCl decreased with increasing salt concentration. These results suggested that sonochemical efficiency decreased with decreasing gas amount in aqueous solution: a negative effect of salts was observed. Because negative and positive effects were induced simultaneously, we concluded that the effects of salts on the rates of sonochemical degradation of phenolic compounds became unclear. The products formed from sonochemical degradation of 4-chlorophenol were also characterized by HPLC analysis. The formation of phenol and 4-chloro-1,3-dihydroxy benzene was confirmed and these concentrations were affected by the

  20. Computation of Accurate Activation Barriers for Methyl-Transfer Reactions of Sulfonium and Ammonium Salts in Aqueous Solution.

    Science.gov (United States)

    Gunaydin, Hakan; Acevedo, Orlando; Jorgensen, William L; Houk, K N

    2007-05-01

    The energetics of methyl-transfer reactions from dimethylammonium, tetramethylammonium, and trimethylsulfonium to dimethylamine were computed with density functional theory, MP2, CBS-QB3, and quantum mechanics/molecular mechanics (QM/MM) Monte Carlo methods. At the CBS-QB3 level, the gas-phase activation enthalpies are computed to be 9.9, 15.3, and 7.9 kcal/mol, respectively. MP2/6-31+G(d,p) activation enthalpies are in best agreement with the CBS-QB3 results. The effects of aqueous solvation on these reactions were studied with polarizable continuum model, generalized Born/surface area (GB/SA), and QM/MM Monte Carlo simulations utilizing free-energy perturbation theory in which the PDDG/PM3 semiempirical Hamiltonian for the QM and explicit TIP4P water molecules in the MM region were used. In the aqueous phase, all of these reactions proceed more slowly when compared to the gas phase, since the charged reactants are stabilized more than the transition structure geometries with delocalized positive charges. In order to obtain the aqueous-phase activation free energies, the gas-phase activation free energies were corrected with the solvation free energies obtained from single-point conductor-like polarizable continuum model and GB/SA calculations for the stationary points along the reaction coordinate.

  1. PEG-salt aqueous two-phase systems: an attractive and versatile liquid-liquid extraction technology for the downstream processing of proteins and enzymes.

    Science.gov (United States)

    Glyk, Anna; Scheper, Thomas; Beutel, Sascha

    2015-08-01

    Nowadays, there is an increasing demand to establish new feasible, efficient downstream processing (DSP) techniques in biotechnology and related fields. Although several conventional DSP technologies have been widely employed, they are usually expensive and time-consuming and often provide only low recovery yields. Hence, the DSP is one major bottleneck for the commercialization of biological products. In this context, polyethylene glycol (PEG)-salt aqueous two-phase systems (ATPS) represent a promising, efficient liquid-liquid extraction technology for the DSP of various biomolecules, such as proteins and enzymes. Furthermore, ATPS can overcome the limitations of traditional DSP techniques and have gained importance for applications in several fields of biotechnology due to versatile advantages over conventional DSP methods, such as biocompatibility, technical simplicity, and easy scale-up potential. In the present review, various practical applications of PEG-salt ATPS are presented to highlight their feasibility to operate as an attractive and versatile liquid-liquid extraction technology for the DSP of proteins and enzymes, thus facilitating the approach of new researchers to this technique. Thereby, single- and multi-stage extraction, several process integration methods, as well as large-scale extraction and purification of proteins regarding technical aspects, scale-up, recycling of process chemicals, and economic aspects are discussed.

  2. Effects of an aqueous leaf extract of Sansevieria senegambica Baker on plasma biochemistry and haematological indices of salt-loaded rats

    Directory of Open Access Journals (Sweden)

    Jude C. Ikewuchi

    2011-11-01

    Full Text Available The effects of an aqueous extract of the leaves of Sansevieria senegambica on plasma marker enzymes, plasma chemistry and the haematological profile of salt-loaded rats were studied. The control group received only a commercial feed, whilst the four test groups received a diet consisting of the commercial feed and salt, although the reference treatment group was reverted to the normal feed at the end of 6 weeks. The extract was orally administered daily at 150 mg/kg or 200 mg/kg body weight to two test groups, respectively; whilst the test control, reference and control groups received equivalent volumes of water by the same route. The extract had no negative effects on markers of liver and kidney functions, but it did produce leukocytosis, significantly increased (p < 0.05 plasma calcium and potassium levels and significantly decreased (p < 0.05 plasma sodium and chloride levels in the test animals compared to the test control animals. This result supports the traditional use of Sansevieria senegambica in the management of hypertension, whilst suggesting that the extract may be a potassium-sparing diuretic whose mechanism of antihypertensive action may be achieved through alteration of plasma sodium and potassium balances, or through calcium-mediated changes in vascular muscle tone.

  3. Effect of Different Water Cluster Structure Zn(NO3)2 Dilute Aqueous Solution on Conformation of Bovine Serum Albumin%不同水团簇结构Zn(NO3)2稀溶液对BSA构象的影响

    Institute of Scientific and Technical Information of China (English)

    阎波; 赵林

    2013-01-01

    The variation of water cluster structure of Zn (NO3) 2 dilute aqueous solution before/after frozen/thawed disposition and its effect on the conformation of bovine serum albumin (BSA) were studied in this paper.The conductivity,density and viscosity of Zn (NO3)2 dilute aqueous solution before/after frozen/thawed disposition were determined to show the variation of water cluster structure of Zn(NO3)2 dilute aqueous solution,which indicated that the freezing/thawing disposition on Zn (NO3) 2 dilute aqueous solution resulted in the obvious increase of conductivity and viscosity,and decrease of density,because of the forming of smaller water cluster structure binded by hydrogen bond in Zn(NO3)2 dilute aqueous solution after frozen/thawed disposition.The conformation of BSA interacted with Zn (NO3) 2 dilute aqueous solution before/after frozen/thawed disposition was studied by laser confocal Raman microspectroscopy,Fourier transform infrared (FTIR) spectroscopy and circular dichroism (CD) spectrum.The result indicated that Zn2+ ions affect the amide Ⅰ bands of BSA,causing the decrease of the α-helices in BSA.The configuration of disulfide bonds and the microenvironment of tyrosine and tryptophan changed owing to the effect of Zn2 + ions on BSA.The freezing/thawing disposition on Zn(NO3)2 dilute queous solution decreased the effect on the conformation of BSA,which caused less decrease of α-helices in BSA amide Ⅰ bands,and weakened the effect on the microenvironment of tyrosine.It can be concluded that the freezeing/thawing disposition on Zn (NO3)2dilute aqueous solution can change the water cluster structure of the dilute aqueous solution,resulting in the change of the physicochemical property of Zn(NO3)2 dilute aqueous solution,and then weakened its effect on the conformation of BSA.%研究了Zn(NO3)2稀溶液冷冻-解冻处理前后水团簇结构的变化和对牛血清白蛋白(BSA)构象的影响.Zn(NO3)2稀溶液经冷冻-解冻处理后,由于小的水分

  4. Complete mapping of crystallization pathways during cholesterol precipitation from model bile: influence of physical-chemical variables of pathophysiologic relevance and identification of a stable liquid crystalline state in cold, dilute and hydrophilic bile salt-containing systems.

    Science.gov (United States)

    Wang, D Q; Carey, M C

    1996-03-01

    Using complementary physical-chemical techniques we defined five different crystallization pathways as functions of time (30 days) and increasing lecithin (egg yolk) content in pathophysiologically relevant model biles super-saturated (cholesterol saturation indices, 1.2 - 2.7) by dilution of approximately equal to 29 g/dl bile salt-lecithin-cholesterol micellar solutions. As evidenced by quasi-elastic light-scattering spectroscopy, supersaturation was heralded by the appearance of unilamellar vesicles. With the lowest lecithin contents, arc-like crystals with habit and density (d 1.030 g/mL) consistent with anhydrous cholesterol appeared first and evolved via helical and tubular crystals to form plate-like cholesterol monohydrate crystals (d 1.045 g/mL). With higher lecithin fractions, cholesterol monohydrate crystals appeared earlier than arc and other transitional crystals. With typical physiological lecithin contents, early liquid crystals (d 1.020 g/mL) were followed by cholesterol monohydrate crystals and subsequent appearances of arc and other intermediate crystals. With higher lecithin contents, liquid crystals were followed by cholesterol monohydrate crystals only, and at the highest lecithin mole fractions, liquid crystals appeared that did not generate solid crystals. Added calcium increased solid crystal number in proportion to its concentration (5 - 20 mM) but did not influence appearance times, crystallization pathways, or micellar cholesterol solubilities. Decreases in temperature (37 degrees --> 4 degrees C), total lipid concentration (7.3 --> 2.4 g/dL), and bile salt hydrophobicity (3 alpha, 12 alpha --> 3 alpha, 7 alpha, 12 alpha --> 3 alpha, 7 beta hydroxylated taurine conjugates) progressively shifted all crystallization pathways to lower lecithin contents, retarded crystallization, and decreased micellar cholesterol solubilities. The lecithin content of mother biles decreased markedly during crystallization especially where liquid crystals were

  5. Separation, concentration and determination of chloramphenicol in environment and food using an ionic liquid/salt aqueous two-phase flotation system coupled with high-performance liquid chromatography.

    Science.gov (United States)

    Han, Juan; Wang, Yun; Yu, Cuilan; Li, Chunxiang; Yan, Yongsheng; Liu, Yan; Wang, Liang

    2011-01-31

    Ionic liquid-salt aqueous two-phase flotation (ILATPF) is a novel, green, non-toxic and sensitive samples pretreatment technique. ILATPF coupled with high-performance liquid chromatography (HPLC) was developed for the analysis of chloramphenicol, which combines ionic liquid aqueous two-phase system (ILATPS) based on imidazolium ionic liquid (1-butyl-3-methylimidazolium chloride, [C(4)mim]Cl) and inorganic salt (K(2)HPO(4)) with solvent sublation. In ILATPF systems, phase behaviors of the ILATPF were studied for different types of ionic liquids and salts. The sublation efficiency of chloramphenicol in [C(4)mim]Cl-K(2)HPO(4) ILATPF was influenced by the types of salts, concentration of K(2)HPO(4) in aqueous solution, solution pH, nitrogen flow rate, sublation time and the amount of [C(4)mim]Cl. Under the optimum conditions, the average sublation efficiency is up to 98.5%. The mechanism of ILATPF contains two principal processes. One is the mechanism of IL-salt ILATPS formation, the other is solvent sublation. This method was practical when applied to the analysis of chloramphenicol in lake water, feed water, milk, and honey samples with the linear range of 0.5-500 ng mL(-1). The method yielded limit of detection (LOD) of 0.1 ng mL(-1) and limit of quantification (LOQ) of 0.3 ng mL(-1). The recovery of CAP was 97.1-101.9% from aqueous samples of environmental and food samples by the proposed method. Compared with liquid-liquid extraction, solvent sublation and ionic liquid aqueous two-phase extraction, ILATPF can not only separate and concentrate chloramphenicol with high sublation efficiency, but also efficiently reduce the wastage of IL. This novel technique is much simpler and more environmentally friendly and is suggested to have important applications for the concentration and separation of other small biomolecules.

  6. 肌醇在氯化钠水溶液中的稀释焓和焓对相互作用%Dilution Enthalpy and Pairwise Enthalpic Interaction of Myo-inositol in Aqueous Sodium Chloride Solution

    Institute of Scientific and Technical Information of China (English)

    郑文清; 曲秀葵; 孙德志∗

    2008-01-01

      The dilution enthalpies of myo-inositol in water and aqueous sodium chloride solutions had been determined with flow–mix-isothermal microcalorimetry at 298.15 K. The enthalpic interaction coefficients in the different concentrations of sodium chloride had been calculated according to the McMillan-Mayer theory. The results showed that enthalpic pairwise interaction coefficients (h2) of myo-inositol are negative in aqueous sodium chloride solutions and values of h2 become more positive with increasing the concentration of sodium chloride. It could be interpreted in terms of interactions of solute with solute and solute with solvent.%  应用微量热法测定了298.15 K时肌醇在纯水和氯化钠水溶液中的稀释焓,根据McMillan-Mayer 理论计算了肌醇在不同浓度的氯化钠溶液中的2到4阶焓相互作用系数.结果表明,肌醇在氯化钠溶液中的焓对相互作用系数h2均为负值,并且随着氯化钠浓度的增大, h2的值呈增大趋势.根据溶质-溶质相互作用和溶质-溶剂相互作用对焓对相互作用系数的变化趋势进行了解释.

  7. Recovery of endo-polygalacturonase using polyethylene glycol-salt aqueous two-phase extraction with polymer recycling

    OpenAIRE

    Wu, You-Ting; Pereira, Martinha; Venâncio, Armando; Teixeira, J. A.

    2000-01-01

    The partitioning behaviour of endo-polygalacturonase (endo-PG) and total protein from a clarified Kluyveromyces marxianus fermentation broth in polyethylene glycol (PEG)-ammonium sulfate and PEG-potassium phosphate (pH=7) aqueous two-phase systems was experimentally investigated. Both the enzyme and total protein partitioned in the bottom phase for these two kinds of systems. The enzyme partitioning coefficient can be lower than 0.01 in PEG8000-(NH4)2SO4 ATPS with a large phase volume ratio a...

  8. Thermodynamic properties of the aqueous solution of potassium salts of some 4-((alkylcarbonyl)amino)-2-hydroxybenzoic acids at 298 and 313 K.

    Science.gov (United States)

    Fisicaro, Emilia; Compari, Carlotta; Viscardi, Guido; Quagliotto, Pierluigi

    2002-11-15

    To understand the aggregation behavior of surface-active ligands with a salycilic polar head, we undertook a systematic study of some classes of anionic surfactants where the presence and the position of the -OH and the carboxylic group differ. This paper reports the dilution heats at 298 and 313 K of aqueous solutions of potassium 4-((alkylcarbonyl)amino)-2-hydroxybenzoate (KPAS-C(n) where n stands for the number of carbon atoms in the chain) in KOH at 0.1 m, measured as a function of concentration. From the experimental data, apparent and partial molar enthalpies vs concentration were obtained. By using a pseudo-phase-transition approach, the enthalpy changes upon micelle formation (DeltaH(m)) and assuming that in the restricted range of temperature examined heat capacities are constant, the heat capacity changes have been obtained. Micelle formation enthalpies are seen to be additive with a group contribution for the methylene group of -1.5+/-0.1 kJ mol(-1) per group at 298 K and -2.3+/-0.1 kJ mol(-1) per group at 313 K, comparable with that obtained for similar anionic compounds in the same experimental conditions and for N-alkylnicotinamide chlorides (cationic surfactants). The -CH(2)- group contribution to the micelle formation heat capacities is -53+/-1 J K(-1) mol(-1).

  9. Quantitative analysis of phosphoric acid esters in aqueous samples by isotope dilution stir-bar sorptive extraction combined with direct analysis in real time (DART)-Orbitrap mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Bridoux, Maxime C., E-mail: maxime.bridoux@cea.fr [CEA, DAM, DIF, F-91297 Arpajon (France); Malandain, Hélène [SANTEN SAS, 1 rue Pierre Fontaine, Bâtiment Genavenir IV, F-91058 Evry (France); Leprince, Françoise; Progent, Frédéric; Machuron-Mandard, Xavier [CEA, DAM, DIF, F-91297 Arpajon (France)

    2015-04-15

    Highlights: • Theory and modeling of organophosphorus SBSE extraction are presented. • Organophosphorus are quantitatively analyzed by isotopic dilution SBSE/DART/Orbitrap-MS. • PDMS coated Twisters™ extract phosphate acid esters in the neutral form from water samples. • Good linearity between concentrations and relative peak areas (0.1–750 ng mL{sup −1}). • This novel SBSE/DART/Orbitrap-MS method should be very valuable for on-site sampling/monitoring - Abstract: A novel hyphenated technique, namely the combination of stir bar sorptive extraction (SBSE) with isotope dilution direct analysis in real time (DART) Orbitrap™ mass spectrometry (OT-MS) is presented for the extraction of phosphoric acid alkyl esters (tri- (TnBP), di- (HDBP), and mono-butyl phosphate (H2MBP)) from aqueous samples. First, SBSE of phosphate esters was performed using a Twister™ coated with 24 μL of polydimethylsiloxane (PDMS) as the extracting phase. SBSE was optimized for extraction pH, phase ratio (PDMS volume/aqueous phase volume), stirring speed, extraction time and temperature. Then, coupling of SBSE to DART/Orbitrap-MS was achieved by placing the Twister™ in the middle of an open-ended glass tube between the DART and the Orbitrap™. The DART mass spectrometric response of phosphate esters was probed using commercially available and synthesized alkyl phosphate ester standards. The positive ion full scan spectra of alkyl phosphate triesters (TnBP) was characterized by the product of self-protonation [M + H]{sup +} and, during collision-induced dissociation (CID), the major fragmentation ions corresponded to consecutive loss of alkyl chains. Negative ionization gave abundant [M − H]{sup −} ions for both HDnBP and H2MnBP. Twisters™ coated with PDMS successfully extracted phosphate acid esters (tri-, di- and mono-esters) granted that the analytes are present in the aqueous solution in the neutral form. SBSE/DART/Orbitrap-MS results show a good linearity between

  10. Initiation of nuclear reactions under laser irradiation of Au nanoparticles in the aqueous solution of Uranium salt

    CERN Document Server

    Simakin, A V

    2010-01-01

    Laser exposure of suspension of either gold or palladium nanoparticles in aqueous solutions of UO2Cl2 of natural isotope abundance was experimentally studied. Picosecond Nd:YAG lasers at peak power from 1011 to 1013 W/cm2 at the wavelength of 1064 and 355 nm were used as well as a visible-range Cu vapor laser at peak power of 1010 W/cm2. The composition of colloidal solutions before and after laser exposure was analyzed using atomic absorption and gamma spectroscopy between 0.06 and 1 MeV range of photon energy. A real-time gamma-spectroscopy was used to characterize the kinetics of nuclear reactions during laser exposure. It was found that laser exposure initiated nuclear reactions involving both 238U and 235U nuclei via different channels in H2O and D2O. The influence of saturation of both the liquid and nanoparticles by gaseous H2 and D2 on the kinetics of nuclear transformations was found. Possible mechanisms of observed processes are discussed.

  11. Tensión Superficial de Soluciones Acuosas Diluidas de Isómeros de Pentanodiol a 283.15 K Surface Tension of Dilute Aqueous Solutions of Pentanediol Isomers at 283.15 K

    Directory of Open Access Journals (Sweden)

    Manuel S Páez

    2009-01-01

    Full Text Available Se estudia el efecto que la posición de los grupos OH tiene sobre la tensión superficial de los isómeros del pentanodiol. La tensión superficial a 283.15 K de soluciones acuosas de 1,2-pentanodiol (12PD, 2,4-pentanodiol (24PD, 1,4-pentanodiol (14PD y 1,5-pentanodiol (15PD fueron medidas como una función de la concentración usando el método de ascenso capilar, en especial en la región diluida. Se evalúa la constante de centros de enlace de acuerdo con el modelo propuesto por Connors para solutos líquidos y los coeficientes de actividad a dilución infinita según el procedimiento sugerido por Gracia-Fadrique. Los resultados muestran la dependencia de la tensión superficial con la posición relativa de los grupos hidroxilos en la molécula de soluto y con el tamaño de la cadena alquílica expuesta al solvente.The effect of the position of OH groups on the surface tension of pentanodiol isomers is studied. Surface tension at 283.15 K of aqueous solutions of 1,2-pentanediol (12PD, 2,4-pentanediol (24PD, 1,4-pentanediol (14PD and 1,5-pentanediol (15PD were measured as a function of the concentration using the method of capillary rise, especially in the diluted region. The binding site constant is evaluated using the model proposed by Connors for liquid solutes and the activity coefficients for infinite dilution according to the procedure suggested by Gracia-Fadrique. The results show the dependence of the surface tension with the relative position of the hydroxylic groups in the solute molecule and with the size of the alquilic chain exposed to the solvent.

  12. 无机金属盐对微波辅助酸预处理毛竹酶解的影响%Effect of Inorganic Salts on Enzymatic Saccharification of Moso Bamboo Pretreated by Microwave-Dilute Acid

    Institute of Scientific and Technical Information of China (English)

    李志强; 费本华; 江泽慧

    2014-01-01

    采用加入无机金属盐的稀酸溶液预处理毛竹,分析预处理后底物的化学组成、预处理后的废液组成、糖降解发酵抑制物的生成量等。结果表明:稀酸预处理主要以脱除半纤维素为主,而对木质素的脱除没有明显效果。当硫酸用量为2%( w/w)、预处理温度为180℃时,竹材中绝大部分半纤维素已被脱除,底物纤维素转化为葡萄糖的收率可达52.72%。加入硫酸铁催化后的稀酸预处理能提高底物的酶水解性能,可使纤维素转化为葡萄糖的收率提高到72.15%。硫酸钠、硫酸亚铁、硫酸铜和硼砂等催化后的稀酸预处理底物的酶水解性能均有不同程度的下降,其中以硫酸铜催化预处理底物的酶水解性能最差。铜离子在预处理中可以被竹材底物吸附,并且在酶水解过程中可以脱附进入水解液中。%Global warming and energy shortage are the main challenges and puzzles that government and the public around the world are facing. It is believed that one of the solutions is to use biomass as a potential renewable energy resource for producing liquid fuels such as bioethanol and biodiesel. Bamboo,with cellulose and hemicellulose as its main components,is a kind of fast growth and cheap renewable resource for bioethanol production. In the study,inorganic salts were studied as promoter in the dilute acid pretreatment of moso bamboo for the enzymatic saccharification. The chemical composition of the substrates and spent liquors,the enzymatic hydrolyability of substrates were analyzed. The results showed that dilute acid pretreatment ( DA) enhances the digestibility of lignocellulose mainly by dissolving hemicellulose and partially prehydrolyzing cellulose. DA has no delignified. The cellulose-to-glucose conversion yield of 2% sulfuric acid( w/w) pretreated substrate was 52. 72%. Sulfuric acid with Fe2 ( SO4 ) 3 pretreated substrate had the higher cellulose-to-glucose conversion yield

  13. The Audio Frequency Conductance Study of Some Metal Succinate Salts in Aqueous Medium at Different Temperatures (Part I: Magnesium, Manganese (II, Barium and Copper Succinates

    Directory of Open Access Journals (Sweden)

    Kosrat N. Kaka

    2013-01-01

    Full Text Available The audio electrical conductances of aqueous solutions of magnesium, manganese II, barium, and copper succinates have been measured at various temperatures in the range of 298.15 K to 313.15 K, using an audio frequency conductance bridge. The evaluation of conductance data was carried out by minimisation technique using the theoretical equations of the complete and modified forms of Pitts (P and Fuoss-Hsia (F-H, each a three-parameter equation, association constant (KA, molar conductance (Λm, and distance parameter (a. Quantitative results showed that these salts do not behave as “strong” electrolytes, and that their dissociations are far from complete. The abnormally low conductances of these electrolytes are not due to the presence of electrically neutral molecules but to the ion-pair formation. The Walden product values, as well as the standard thermodynamics functions (ΔH∘, ΔG∘, ΔS∘ for the association reaction at the four temperatures studied, have been evaluated.

  14. Comparison of microenvironments of aqueous sodium dodecyl sulfate micelles in the presence of inorganic and organic salts: a time-resolved fluorescence anisotropy approach.

    Science.gov (United States)

    Dutt, G B

    2005-11-08

    Microenvironments of aqueous sodium dodecyl sulfate (SDS) micelles was examined in the presence of additives such as sodium chloride and p-toluidine hydrochloride (PTHC) by monitoring the fluorescence anisotropy decays of two hydrophobic probes, 2,5-dimethyl-1,4-dioxo-3,6-diphenylpyrrolo[3,4-c]pyrrole (DMDPP) and coumarin 6 (C6). It has been well-established that SDS micelles undergo a sphere-to-rod transition and that their mean hydrodynamic radius increases from 19 to 100 A upon the addition of 0.0-0.7 M NaCl at 298 K. A similar size and shape transition is induced by PTHC at concentrations that are 20 times lower compared to that of NaCl. This study was undertaken to find out how the microviscosity of the micelles is influenced under these circumstances. It was noticed that the microviscosity of the SDS/NaCl system increased by approximately 45%, whereas there was a less than 10% variation in the microviscosity of the SDS/PTHC system. The large increase in the microviscosity of the former system with salt concentration has been rationalized on the basis of the high concentration of sodium ions in the headgroup region of the micelles and their ability to strongly coordinate with the water present in this region, which decreases the mobility of the probe molecules.

  15. Direct Purification of Pectinase from Mango (Mangifera Indica Cv. Chokanan Peel Using a PEG/Salt-Based Aqueous Two Phase System

    Directory of Open Access Journals (Sweden)

    Abdul Manap Mohd Yazid

    2011-10-01

    Full Text Available An Aqueous Two-Phase System (ATPS was employed for the first time for the separation and purification of pectinase from mango (Mangifera Indica Cv. Chokanan peel. The effects of different parameters such as molecular weight of the polymer (polyethylene glycol, 2,000–10,000, potassium phosphate composition (12–20%, w/w, system pH (6–9, and addition of different concentrations of neutral salts (0–8%, w/w on partition behavior of pectinase were investigated. The partition coefficient of the enzyme was decreased by increasing the PEG molecular weight. Additionally, the phase composition showed a significant effect on purification factor and yield of the enzyme. Optimum conditions for purification of pectinase from mango peel were achieved in a 14% PEG 4000-14% potassium phosphate system using 3% (w/w NaCl addition at pH 7.0. Based on this system, the purification factor of pectinase was increased to 13.2 with a high yield of (97.6%. Thus, this study proves that ATPS can be an inexpensive and effective method for partitioning of pectinase from mango peel.

  16. Direct purification of pectinase from mango (Mangifera Indica Cv. Chokanan) peel using a PEG/salt-based Aqueous Two Phase System.

    Science.gov (United States)

    Mehrnoush, Amid; Sarker, Md Zaidul Islam; Mustafa, Shuhaimi; Yazid, Abdul Manap Mohd

    2011-10-10

    An Aqueous Two-Phase System (ATPS) was employed for the first time for the separation and purification of pectinase from mango (Mangifera Indica Cv. Chokanan) peel. The effects of different parameters such as molecular weight of the polymer (polyethylene glycol, 2,000-10,000), potassium phosphate composition (12-20%, w/w), system pH (6-9), and addition of different concentrations of neutral salts (0-8%, w/w) on partition behavior of pectinase were investigated. The partition coefficient of the enzyme was decreased by increasing the PEG molecular weight. Additionally, the phase composition showed a significant effect on purification factor and yield of the enzyme. Optimum conditions for purification of pectinase from mango peel were achieved in a 14% PEG 4000-14% potassium phosphate system using 3% (w/w) NaCl addition at pH 7.0. Based on this system, the purification factor of pectinase was increased to 13.2 with a high yield of (97.6%). Thus, this study proves that ATPS can be an inexpensive and effective method for partitioning of pectinase from mango peel.

  17. Cr(VI) sorption behavior from aqueous solutions onto polymeric microcapsules containing a long-chain quaternary ammonium salt: Kinetics and thermodynamics analysis

    Energy Technology Data Exchange (ETDEWEB)

    Barassi, Giancarlo; Valdes, Andrea; Araneda, Claudio; Basualto, Carlos; Sapag, Jaime; Tapia, Cristian [Laboratorio de Operaciones Unitarias, Facultad de Ciencias Quimicas y Farmaceuticas, Universidad de Chile, Av. Vicuna Mackenna 20, Santiago (Chile); Valenzuela, Fernando, E-mail: fvalenzu@uchile.cl [Laboratorio de Operaciones Unitarias, Facultad de Ciencias Quimicas y Farmaceuticas, Universidad de Chile, Av. Vicuna Mackenna 20, Santiago (Chile)

    2009-12-15

    This work studies the adsorption of Cr(VI) ions from an aqueous acid solution on hydrophobic polymeric microcapsules containing a long-chain quaternary ammonium salt-type extractant immobilized in their pore structure. The microcapsules were synthesized by adding the extractant Aliquat 336 during the in situ radical copolymerization of the monomers styrene (ST) and ethylene glycol dimethacrylate (EGDMA). The microcapsules, which had a spherical shape with a rough surface, behaved as efficient adsorbents for Cr(VI) at the tested temperatures. The results of kinetics experiments carried out at different temperatures showed that the adsorption process fits well to a pseudo-second-order with an activation energy of 82.7 kJ mol{sup -1}, confirming that the sorption process is controlled by a chemisorption mechanism. Langmuir's isotherms were found to represent well the experimentally observed sorption data. Thermodynamics parameters, namely, changes in standard free energy ({Delta}G{sup 0}), enthalpy ({Delta}H{sup 0}), and entropy ({Delta}S{sup 0}), are also calculated. The results indicate that the chemisorption process is spontaneous and exothermic. The entropy change value measured in this study shows that metal adsorbed on microcapsules leads to a less chaotic system than a liquid-liquid extraction system.

  18. Radiolysis of paracetamol in dilute aqueous solution

    Science.gov (United States)

    Szabó, László; Tóth, Tünde; Homlok, Renáta; Takács, Erzsébet; Wojnárovits, László

    2012-09-01

    Using radiolytic experiments hydroxyl radical (main reactant in advanced oxidation processes) was shown to effectively destroy paracetamol molecules. The basic reaction is attachment to the ring. The hydroxy-cyclohexadienyl radical produced in the further reactions may transform to hydroxylated paracetamol derivatives or to quinone type molecules and acetamide. The initial efficiency of aromatic ring destruction in the absence of dissolved O2 is c.a. 10%. The efficiency is 2-3 times higher in the presence of O2 due to its reaction with intermediate hydroxy-cyclohexadienyl radical and the subsequent ring destruction reactions through peroxi radical. Upon irradiation the toxicity of solutions at low doses increases with the dose and then at higher doses it decreases. This is due to formation of compounds with higher toxicity than paracetamol (e.g. acetamide, hidroquinone). These products, however, are highly sensitive to irradiation and degrade easily.

  19. Free energetics of carbon nanotube association in aqueous inorganic NaI salt solutions: Temperature effects using all-atom molecular dynamics simulations.

    Science.gov (United States)

    Ou, Shu-Ching; Cui, Di; Wezowicz, Matthew; Taufer, Michela; Patel, Sandeep

    2015-06-15

    In this study, we examine the temperature dependence of free energetics of nanotube association using graphical processing unit-enabled all-atom molecular dynamics simulations (FEN ZI) with two (10,10) single-walled carbon nanotubes in 3 m NaI aqueous salt solution. Results suggest that the free energy, enthalpy and entropy changes for the association process are all reduced at the high temperature, in agreement with previous investigations using other hydrophobes. Via the decomposition of free energy into individual components, we found that solvent contribution (including water, anion, and cation contributions) is correlated with the spatial distribution of the corresponding species and is influenced distinctly by the temperature. We studied the spatial distribution and the structure of the solvent in different regions: intertube, intratube and the bulk solvent. By calculating the fluctuation of coarse-grained tube-solvent surfaces, we found that tube-water interfacial fluctuation exhibits the strongest temperature dependence. By taking ions to be a solvent-like medium in the absence of water, tube-anion interfacial fluctuation shows similar but weaker dependence on temperature, while tube-cation interfacial fluctuation shows no dependence in general. These characteristics are discussed via the malleability of their corresponding solvation shells relative to the nanotube surface. Hydrogen bonding profiles and tetrahedrality of water arrangement are also computed to compare the structure of solvent in the solvent bulk and intertube region. The hydrophobic confinement induces a relatively lower concentration environment in the intertube region, therefore causing different intertube solvent structures which depend on the tube separation. This study is relevant in the continuing discourse on hydrophobic interactions (as they impact generally a broad class of phenomena in biology, biochemistry, and materials science and soft condensed matter research), and

  20. Development of a robust ionic liquid-based dispersive liquid-liquid microextraction against high concentration of salt for preconcentration of trace metals in saline aqueous samples: Application to the determination of Pb and Cd

    Energy Technology Data Exchange (ETDEWEB)

    Yousefi, Seyed Reza [School of Chemistry, University College of Science, University of Tehran, Tehran (Iran, Islamic Republic of); Shemirani, Farzaneh, E-mail: shemiran@khayam.ut.ac.ir [School of Chemistry, University College of Science, University of Tehran, Tehran (Iran, Islamic Republic of)

    2010-06-11

    A new ionic liquid-based dispersive liquid-liquid microextraction method was developed for preconcentration and determination of compounds in aqueous samples containing very high salt concentrations. This method can solve the problems associated with the limited application of the conventional IL-based DLLME in these samples. This is believed to arise from dissolving of the ionic liquids in aqueous samples with high salt content. In this method, the robustness of microextraction system against high salt concentration (up to 40%, w/v) is increased by introducing a common ion of the ionic liquid into the sample solution. The proposed method was applied satisfactorily to the preconcentration of lead and cadmium in saline samples. After preconcentration, the settled IL-phase was dissolved in 100 {mu}L ethanol and aspirated into the flame atomic absorption spectrometer (FAAS) using a home-made microsample introduction system. Several variables affecting the microextraction efficiency were investigated and optimized. Under the optimized conditions and preconcentration of only 10 mL of sample, the enhancement factors of 273 and 311 and the detection limits of 0.6 {mu}g L{sup -1} and 0.03 {mu}g L{sup -1} were obtained for lead and cadmium, respectively. Validation of the method was performed by both an analysis of a certified reference material (CRM) and comparison of results with those obtained by ISO standard method.

  1. Ionic liquid and aqueous two-phase extraction based on salting-out coupled with high-performance liquid chromatography for the determination of seven rare ginsenosides in Xue-Sai-Tong injection.

    Science.gov (United States)

    Li, Lan-Jie; Jin, Yong-Ri; Wang, Xiao-Zhong; Liu, Ying; Wu, Qian; Shi, Xiao-Lei; Li, Xu-Wen

    2015-09-01

    A method of ionic liquid salt aqueous two-phase extraction coupled with high-performance liquid chromatography has been developed for the analysis of seven rare ginsenosides including Rg6 , F4 , 20(S)-Rg3 , 20(R)-Rg3 , Rk3 , Rk1 , and Rg5 in Xue-Sai-Tong injection. The injection was mixed with ionic liquid 1-butyl-3-methylimidazolium bromide aqueous solution, and a mixture was obtained. With the addition of sodium dodecyl sulfate and dipotassium phosphate into the mixture, the aqueous two-phase mixture was formed after ultrasonic treatment and centrifuged. Rare ginsenosides were extracted into the upper phase. To obtain a high extraction factors, various influences were considered systematically, such as the volume of ionic liquid, the category and amount of salts, the amount of sodium dodecyl sulfate, the pH value of system, and the time of ultrasonic treatment. Under the optimal condition, rare ginsenosides in Xue-Sai-Tong injection were enriched and detected, the recoveries of seven rare ginsenosides ranged from 90.05 to 112.55%, while relative standard deviations were lower than 2.50%. The developed method was reliable, rapid and sensitive for the determination of seven rare ginsenosides in the injections.

  2. Aqueous solubility study of salts of benzylamine derivatives and p-substituted benzoic acid derivatives using X-ray crystallographic analysis

    DEFF Research Database (Denmark)

    Parshad, Henrik; Frydenvang, Karla Andrea; Liljefors, Tommy

    2004-01-01

    than those reported for the corresponding salts of benzylamine (I). Thermal analysis indicated that the increased solubility was caused by reduced crystal lattice energy, which was most likely due to the reduced number of strong hydrogen bonds of the salt of (II) and (III). X-ray crystallographic...... analysis of p-hydroxybenzoic acid salt of (I), (II) and (III) suggested that the reduced number of hydrogen bonds caused the apparent higher solubility. Further analyses of seven salts of (I) were performed. It was not possible to identify any relationship between the number of hydrogen bonds...

  3. Experimental study of evaporation of distilled water and 10% NaCl and СaCl2 aqueous salt solutions droplets under their free falling on a heated surface

    Directory of Open Access Journals (Sweden)

    Feoktistov D.V.

    2017-01-01

    Full Text Available The paper presents the experimental results of evaporation of distilled water and 10% aqueous salt solutions of NaCl and СaCl2 droplets under their free falling on a heated surface. It is proved that it is more expedient to conduct the experimental research in this field according to classical multifactorial experiment. Laser treatment of surfaces is found to increase the evaporation rate and to biases the point of boiling crisis in the region of lower surface temperatures. In this case, in the conditions of boiling crisis the frequency of contact of a droplet with a heated surface will decrease.

  4. Pairing heterocyclic cations with closo-icosahedral borane and carborane anions. i. benchtop aqueous synthesis of binary triazolium and imidazolium salts with limited water solubility.

    Science.gov (United States)

    Shackelford, Scott A; Belletire, John L; Boatz, Jerry A; Schneider, Stefan; Wheaton, Amanda K; Wight, Brett A; Hudgens, Leslie M; Ammon, Herman L; Strauss, Steven H

    2009-06-18

    Ten new salts that pair triazolium and imidazolium cations with closo-icosahedral anions [B(12)H(12)](2-) and [CB(11)H(12)](-) were synthesized in water solvent using an open-air, benchtop method. These unreported [Heterocyclium](2)[B(12)H(12)] and [Heterocyclium][CB(11)H(12)] salts extend reports of [Imidazolium][CB(11)H(12)] and [Pyridinium][CB(11)H(12)] salts that were synthesized in anhydrous organic solvents under an inert atmosphere with glovebox or Schlenk techniques. Spectroscopic data, melting points, and densities are reported for each salt. Single-crystal X-ray structures are provided for the five new [B(12)H(12)](2-) salts.

  5. Experimental determination of salt partition coefficients between aqueous fluids, ice VI and ice VII: implication for the composition of the deep ocean and the geodynamics of large icy moons and water rich planets

    Science.gov (United States)

    Journaux, Baptiste; Daniel, Isabelle; Cardon, Hervé; Petitgirard, Sylvain; Perrillat, Jean-Philippe; Caracas, Razvan; Mezouar, Mohamed

    2015-04-01

    The potential habitability of extraterrestrial large aqueous reservoir in icy moons and exoplanets requires an input of nutrients and chemicals that may come from the rocky part of planetary body. Because of the presence of high pressure (HP) water ices (VI, VII, etc.) between the liquid ocean and the silicates, such interactions are considered to be limited in large icy moons, like Ganymede and Titan, and water rich exoplanets. In the case of salty-rich oceans, recent experimental and modeling works have shown that aqueous fluids can be stable at higher pressures [1, 2]. This can ultimately allow direct interaction with the rocky core of icy moons. This effect is nevertheless limited and for larger bodies such as water rich exoplanets with much higher pressures in their hydrosphere, HP ice should be present between the rocky core and a putative ocean. Salts are highly incompatible with low pressure ice Ih, but recent experimental work has shown that alkali metal and halogen salts are moderately incompatible with ice VII, that can incorporate up to several mol/kg of salts [3, 4, 5]. As far as we know, no similar study has been done on ice VI, a HP ice phase expected inside large icy moons. We present here the first experimental data on the partition coefficient of RbI salt between aqueous fluids, ice VI and ice VII using in-situ synchrotron X-Ray single crystal diffraction and X-Ray fluorescence mapping (ESRF - ID-27 beam line [6]). Our experiment enable us to observe a density inversion between ice VI and the salty fluid, and to measure the values of salt partition coefficients between the aqueous fluid and ice VI (strongly incompatible) and ice VII (moderately incompatible). Using the volumes determined with X-Ray diffraction, we were able to measure the density of salty ice VI and ice VII and determine that salty ice VI is lighter than pure H2O ice VI. These results are very relevant for the study of water rich planetary bodies interior because the partition

  6. 异丙醇/盐双水相分离制备高色价栀子黄%Separation of Gardenia Yellow by Isopropanol Alcohol/Salt Aqueous Two-Phase System

    Institute of Scientific and Technical Information of China (English)

    郭晶莹; 张红萍

    2016-01-01

    Abstrat:Gardenia yellow was separated by employing isopropanol-salt aqueous two-phase system. The factors such as kinds of salt, concentration of the salt, pH and temperture on the gardenia yellow separation efficiency were investigated, and the gardenia yellow was analyzed by spectrophotometric method and HPLC. The results showed that the aqueous two-phase system which was formed by isopropanol alcohol(2mL) and sodium citrate (1.6g)was effective for the separation of gardenia yellow from gardenia fruit in 35℃and pH=8.7,and the color value and the OD of the gardenia yellow were 542 and 0.382,respectively.%采用异丙醇/盐组成的双水相体系分离栀子黄。综合考察了盐的种类、浓度、pH值和温度等因素对栀子黄分离效果的影响,并且采用紫外-可见分光光度法和HPLC对异丙醇/盐双水相体系分离得到的栀子黄进行评价。结果表明,在35℃条件下由1.6g的柠檬酸三钠和2mL的异丙醇组成双水相体系,pH等于8.7,分离得到栀子黄和OD值分别为0.382、542。

  7. Study on aqueous two-phase extraction of L-phenylalanine by polyethylene glycol/salt system%聚乙二醇/盐双水相萃取L-苯丙氨酸的研究

    Institute of Scientific and Technical Information of China (English)

    孙晨; 刘文举; 刘宁宁

    2012-01-01

    研究了聚乙二醇/盐双水相体系的成相行为及L-苯丙氨酸在双水相中的分配规律,其中包括聚乙二醇的分子量、聚乙二醇质量分数、盐的种类及加入量、L-苯丙氨酸初始浓度和pH对萃取分离的影响。当聚乙二醇1000的质量分数为27%,磷酸氢二钾的质量浓度为O.15g/mL,L-苯丙氨酸的质量浓度为10g/L,体系的pH为8.5时,L-苯丙氨酸的萃取率最高为99.5%,分配系数最大为186.5。%An aqueous two- phase system of polyethylene glycol (PEG)/salt with the behavior of forming aqueous two-phase and the distribution rules of L-phenylalanine in the aqueous two-phase system were studied.Effects of the molecular weight of polyethylene glycol ,the mass fraction of polyethylene glycol ,the types and concentrations of salts,the initial concentration of L-phenylalanine and pH value were investigated.When the mass fraction of PEG1000 was 27% ,the mass concentration of K2HPO4was 0.]5g/mL,the initial concentration of L-phenylalanine was 10g/L and pH value was about 8.5,the highest extraction yield of L-phenylalanine could reach 99.5 %, partition coefficient of L-phenylalanine could reach 186.5.

  8. Moderation of hematological and plasma biochemical indices of sub-chronic salt-loaded rats, by an aqueous extract of the leaves of Acalypha wilkesiana ‘Godseffiana’ Muell Arg (Euphorbiaceae)

    Institute of Scientific and Technical Information of China (English)

    Ikewuchi Jude C

    2013-01-01

    Objective: To investigate the effects of an aqueous leaf extract of Acalypha wilkesiana (A. wilkesiana) on plasma chemistry and hematological indices of sub-chronic salt-loaded rats.Method:The control group received a diet consisting 100% of the commercial feed, while the four test groups were received a diet consisting 8% salt and 92% commercial feed all through, except for the reference treatment group that had its salt-loading discontinued after six weeks. The extract was orally administered daily at 200 and 250 mg/kg body weight; while the test control, reference and control groups received appropriate volumes of water by the same route.Results:The extract had no negative effects on markers of liver and kidney functions, produced hemoconcentration, significantly higher (P<0.05) plasma calcium and potassium levels, and significantly lower (P<0.05) plasma sodium and chloride levels in the test animals compared to test control. Conclusions: This result supports the traditional use of A. wilkesiana in the management of hypertension and suggests that the extract may be a potassium sparing diuretic whose mechanism of antihypertensive action may be via alteration of plasma sodium and potassium balances or calcium mediated alteration in vascular muscle tone.

  9. 以蔗糖飞灰吸附剂分离废水中的β-萘磺酸%Removal ofβ-Naphthalenesulfonic Acid from Aqueous Dilute Solution Using Bagasse Fly Ash

    Institute of Scientific and Technical Information of China (English)

    李长海; 史鹏飞

    2002-01-01

    Bagasse fly ash was converted into an inexpensive adsorbent and utilized for the removal of β-naphthalenesulfonic acid in dilute solution. The effect of pH, temperature, adsorbent concentration, and co-existed acids on the removal ofβ-naphthalenesulfonic acid was examined. The adsorption data have been correlated with both Langmuir and Freundlich adsorption models. Thermodynamic parameters obtained indicate the feasibility of the process, and kinetic studies provided the necessary mechanistic information of the removal process.

  10. 双水相体系在无机盐分离中的应用%Application of Aqueous - two Phase System in the Separation of Inorganic Salts

    Institute of Scientific and Technical Information of China (English)

    史许娜; 韩清华

    2016-01-01

    Different separation methods of potassium chloride and ammonium chloride mixture are ana-lyzed. The present situation for separating mixed solution of potassium chloride and ammonium chloride by aqueous two - phase system(1 - propanol - KCl - NH4 Cl - H2 O aqueous two - phase system)is intro-duced,and the application of aqueous two - phase system is expanded.%分析了氯化钾和氯化铵混合溶液的不同分离方法,介绍了双水相体系(正丙醇—氯化钾—氯化铵—水双水相体系)对该混合溶液的分离现状,拓展了双水相体系的应用范围。

  11. Effects of Bile Salt Sodium Glycodeoxycholate on the Self-Assembly of PEO-PPO-PEO Triblock Copolymer P123 in Aqueous Solution.

    Science.gov (United States)

    Bayati, Solmaz; Galantini, Luciano; Knudsen, Kenneth D; Schillén, Karin

    2015-12-22

    A comprehensive experimental study on the interaction between the PEO-PPO-PEO block copolymer P123 (EO20PO68EO20) and the anionic bile salt sodium glycodeoxycholate (NaGDC) in water has been performed. The work was aimed at investigating the suitability of using P123 as bile salt sequestrant beside the fundamental aspects of PEO-PPO-PEO block copolymer-bile salt interactions. Various experimental techniques including dynamic and static light scattering, small-angle X-ray scattering, and differential scanning calorimetry (DSC) were employed in combination with electrophoretic mobility measurements. The system was investigated at a constant P123 concentration of 1.74 mM and with varying bile salt concentrations up to approximately 250 mM NaGDC (or a molar ratio n(NaGDC)/n(P123) = 144). In the mixed P123-NaGDC solutions, the endothermic process related to the self-assembly of P123 was observed to gradually decrease in enthalpy and shift to higher temperatures upon progressive addition of NaGDC. To explain this effect, the formation of NaGDC micelles carrying partly dehydrated P123 unimers was proposed and translated into a stoichiometric model, which was able to fit the experimental DSC data. In the mixtures at low molar ratios, NaGDC monomers associated with the P123 micelle forming a charged "P123 micelle-NaGDC" complex with a dehydrated PPO core. These complexes disintegrated upon increasing NaGDC concentration to form small "NaGDC-P123" complexes visualized as bile salt micelles including one or a few P123 copolymer chains.

  12. IUPAC-NIST Solubility Data Series. 90. Hydroxybenzoic Acid Derivatives in Binary, Ternary, and Multicomponent Systems. Part I. Hydroxybenzoic Acids, Hydroxybenzoates, and Hydroxybenzoic Acid Salts in Water and Aqueous Systems

    Science.gov (United States)

    Goto, Rensuke; Fukuda, Hiroshi; Königsberger, Erich; Königsberger, Lan-Chi

    2011-03-01

    The solubility data for well-defined binary, ternary, and multicomponent systems of solid-liquid type are reviewed. One component, which is 2-, 3-, and 4-hydroxybenzoic acids, 4-hydroxybenzoate alkyl esters (parabens), or hydroxybenzoic acid salts, is in the solid state at room temperature and another component is liquid water, meaning that all of the systems are aqueous solutions. The ternary or multicomponent systems include organic substances of various classes (hydrocarbons of several structural types, halogenated hydrocarbons, alcohols, acids, ethers, esters, amides, and surfactants) or inorganic substances. Systems reported in the primary literature from 1898 through 2000 are compiled. For seven systems, sufficient binary data for hydroxybenzoic acids or parabens in water are available to allow critical evaluation. Almost all data are expressed as mass and mole fractions as well as the originally reported units, while some data are expressed as molar concentration.

  13. 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

    Science.gov (United States)

    Campos, Sandro X.; Vieira, Eny M.; Cordeiro, Paulo J. M.; Rodrigues-Fo, Edson; Murgu, Michael

    2003-12-01

    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 1.13×10 -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.

  14. Understanding and Exploitation of Neighboring Heteroatom Effect for the Mild N-Arylation of Heterocycles with Diaryliodonium Salts under Aqueous Conditions: A Theoretical and Experimental Mechanistic Study.

    Science.gov (United States)

    Bihari, Tamás; Babinszki, Bence; Gonda, Zsombor; Kovács, Szabolcs; Novák, Zoltán; Stirling, András

    2016-07-01

    The mechanism of arylation of N-heterocycles with unsymmetric diaryliodonium salts is elucidated. The fast and efficient N-arylation reaction is interpreted in terms of the bifunctionality of the substrate: The consecutive actions of properly oriented Lewis base and Brønsted acid centers in sufficient proximity result in the fast and efficient N-arylation. The mechanistic picture points to a promising synthetic strategy where suitably positioned nucleophilic and acidic centers enable functionalization, and it is tested experimentally.

  15. Catalysis and stability of an alkaline protease from a haloalkaliphilic bacterium under non-aqueous conditions as a function of pH, salt and temperature.

    Science.gov (United States)

    Pandey, Sandeep; Rakholiya, Kalpna D; Raval, Vikram H; Singh, Satya P

    2012-09-01

    A haloalkaliphilic bacterium, isolated from Coastal Gujarat (India) was identified as Oceanobacillus sp. (GQ162111) based on 16S rRNA gene sequence. The organism grew and secreted extra cellular protease in presence of various organic solvents. At 30% (v/v) concentration of hexane, heptane, isooctane, dodecane and decane, significant growth and protease production was evident. The alkaline protease was purified in a single step on phenyl sepharose 6 FF with 28% yield. The molecular mass as judged by SDS-PAGE was 30 kDa. The temperature optimum of protease was 50°C and the enzyme retained 70% activity in 10% (v/v) isooctane. Effect of salt and pH was investigated in combination to assess the effect of isooctane. In organic solvents, the enzyme was considerably active at pH 8-11, with optimum activity at pH 10. Salt at 2 M was optimum for activity and enzyme maintained significant stability up to 18 h even at 3 M salt concentration. Patters of growth, protease production, catalysis and stability of the enzyme are presented. The study resumes significance as limited information is available on the interaction of haloalkaliphilic bacteria and their enzymes with organic solvents.

  16. Spectral features of guanidinium-carboxylate salt bridges. The combined ATR-IR and theoretical studies of aqueous solution of guanidinium acetate

    Science.gov (United States)

    Levina, Elena O.; Lokshin, Boris V.; Mai, Bich D.; Vener, Mikhail V.

    2016-08-01

    The spectrum of guanidinium acetate in aqueous solution has been recorded by attenuated total reflectance infrared spectroscopy (ATR-IR). Assignments of the bands have been done using the polarizable continuum model (PCM). Three IR intensive bands at 1670, 1550, and 1410 cm-1 are associated with stretching and bending vibrations of the groups forming a ring of six heavy atoms of the bidentate configuration of guanidinium acetate. The relatively weak broad band near 2200 cm-1 is tentatively assigned to the stretching vibration of the Nsbnd H⋯O fragment of the hydrogen-bonded ion pairs.

  17. Hybridizing pines with diluted pollen

    Science.gov (United States)

    Robert Z. Callaham

    1967-01-01

    Diluted pollens would have many uses by the tree breeder. Dilutions would be particularly advantageous in making many controlled pollinations with a limited amount of pollen. They also would be useful in artificial mass pollinations of orchards or single trees. Diluted pollens might help overcome troublesome genetic barriers to crossing. Feasibility o,f using diluted...

  18. An Investigation of Ion-Pairing of Alkali Metal Halides in Aqueous Solutions Using the Electrical Conductivity and the Monte Carlo Computer Simulation Methods.

    Science.gov (United States)

    Gujt, Jure; Bešter-Rogač, Marija; Hribar-Lee, Barbara

    2014-02-01

    The ion pairing is, in very dilute aqueous solutions, of rather small importance for solutions' properties, which renders its precise quantification quite a laborious task. Here we studied the ion pairing of alkali halides in water by using the precise electric conductivity measurements in dilute solutions, and in a wide temperature range. The low-concentration chemical model was used to analyze the results, and to estimate the association constant of different alkali halide salts. It has been shown that the association constant is related to the solubility of salts in water and produces a 'volcano relationship', when plotted against the difference between the free energy of hydration of the corresponding individual ions. The computer simulation, using the simple MB+dipole water model, were used to interprete the results, to find a microscopic basis for Collins' law of matching water affinities.

  19. Processing method for molten salt waste

    Energy Technology Data Exchange (ETDEWEB)

    Ito, Shuichi; Sawa, Toshio; Hoshikawa, Tadahiro; Suzuoki, Akira

    1999-01-06

    The present invention concerns a processing method for selectively adsorbing and removing radioactive metal ingredients contained in high temperature molten salts by an inorganic ion exchanger and separating radioactive metal ingredients from the molten salts as high level radioactive wastes upon reprocessing of spent nuclear fuels by using molten salts. The molten salts occluded in the inorganic ion exchanger are desorbed with highly purified water. Successively, saturation adsorbed radioactive metal ingredients are desorbed by an aqueous solution of alkali metal salt or an aqueous solution of alkaline earth metal salt. The desorbed molten salts and radioactive metal ingredients are formed into at least two kinds of radioactive waste solidification materials depending on each of radioactivity level. As the inorganic ion exchanger, at least one of aluminosilicate and hydroxides is used. Then, molten salt wastes generated upon a dry-type reprocessing can be processed as a stable borosilicate glass solidification material or as a similar homogeneous solid material. (T.M.)

  20. 天花粉蛋白的盐析工艺和亲和双水相分离工艺%Salting-out process and affinity aqueous two-phase extraction process of trichosanthin

    Institute of Scientific and Technical Information of China (English)

    汪苗苗; 丁玉

    2012-01-01

    In recent years, clinical studies showed that trichosanthin's has anti-cancer and anti- HIV virus function. The trichosanthin's production needs to be studied to meet the market needs. This experiment used two steps of tricho-santhin extraction a) purification trichosanthin with ammonium sulfate precipitation, b) affinity aqueous two-phase extraction after ammonium sulfate coarse separation. The extraction process was optimized and gel electrophoresis was used in identifying the purity and molecular weight. The salting-out method and affinity aqueous two-phase separation method were compared. The best conditions for salting-out separation were: solid-liquid ratio 1:12, soaking time 24 hours, pH 5, and the yield 0. 8ml/g. The best affinity aqueous two-phase separation conditions were; the percentage of Cibacron Blue F3GA-Tween 80 was 8% , the content of Tween 80 in aqueous two-phase was 4. 0% , content of ( NH4 )2SO4 was 2.0mol/L, mixing time 9h, stripping sodium content 0. 5mol/L, the anti-extraction time 8h, yield was 0.6mg/g. The electrophoresis showed the products had a high purity.%近年,随着天花粉蛋白(TCS)在抗癌细胞和HIV病毒方面的临床性研究进展,天花粉蛋白生产工艺也需在保证效益的前提下精细化.本实验利用硫酸铵分级沉淀、硫酸铵粗提后亲和双水相进一步纯化,得到精制的天花粉蛋白.并对提取工艺进行了优化,最后利用SDS聚丙烯酰胺凝胶电泳对其纯度进行了鉴定以及相对分子质量的测定,并对比了盐析法和亲和双水相分离法,研究结果表明:硫酸铵沉淀法最佳分离条件为固液比为1∶12、浸泡时间为24h、pH在5左右,最终得率0.8mg/g;亲和萃取最佳条件:染料CibacronBlue F3GA-吐温80在成相吐温80中的含量8%,成相吐温80的占双水相含量为4.0%,(NH4)2S04的含量2.0mol/L,充分混合的时间9h,反萃取氯化钠的含量为0.5mol/L,反萃取的时间为8h,得率0.6mg/g,但凝胶电泳显示其纯度较高.

  1. Effect of alkyl chain length and temperature on the thermodynamic properties of ionic liquids 1-alkyl-3-methylimidazolium bromide in aqueous and non-aqueous solutions 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; Shekaari, Hemayat [Department of Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of); Hosseini, Rahim [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)

    2009-02-15

    The alkyl chain length of 1-alkyl-3-methylimidazolium bromide ([Rmim][Br], R = propyl (C{sub 3}), hexyl (C{sub 6}), heptyl (C{sub 7}), and octyl (C{sub 8})) was varied to prepare a series of room-temperature ionic liquids (RTILs), and experimental measurements of density and speed of sound at different temperatures ranging from (288.15 to 308.15) K for their aqueous and methanolic solutions in the dilute concentration region (0.01 to 0.30) mol . kg{sup -1} were taken. The values of the compressibilities, expansivity and apparent molar properties for [C{sub n}mim][Br] in aqueous and methanolic solutions were determined at the investigated temperatures. The obtained apparent molar volumes and apparent molar isentropic compressibilities were fitted to the Redlich-Mayer and the Pitzer's equations from which the corresponding infinite dilution molar properties were obtained. The values of the infinite dilution molar properties were used to obtain some information about solute-solvent and solute-solute interactions. The thermodynamic properties of investigated ionic liquids in aqueous solutions have been compared with those in methanolic solutions. Also, the comparison between thermodynamic properties of investigated solutions and those of electrolyte solutions, polymer solutions, cationic surfactant solutions and tetraalkylammonium salt solutions have been made.

  2. Extraction of Tartrazine from Food Colorants by PEG/Salt Aqueous Two-Phase System%PEG/盐双水相萃取食用色素柠檬黄的研究

    Institute of Scientific and Technical Information of China (English)

    姜彬; 李冬梅; 冯志彪

    2014-01-01

    采用PEG/盐双水相体系萃取食用色素柠檬黄。考察了成相物质对柠檬黄吸光度的影响,在此基础上考察了PEG相对分子量、PEG浓度、盐的种类及浓度、p H 对萃取效果的影响,确定了萃取柠檬黄的最佳条件:18% PEG2000,15%(NH4)2SO4,pH 为6。该体系对柠檬黄色萃取效果不受外加无机盐的影响,但表面活性剂的存在对萃取效果有较大影响。%An aqueous two-phase system (ATPS )is presented with polyethylene glycol (PEG )and salt for the extraction of tartrazine in this paper.The extraction of tartrazine in ATPS is investigated. Concentration of (NH4 )2 SO4 and PEG,pH value and other factors are evaluated to determine their effects on the extraction yield of tartrazine.The results show that the extraction yield strongly de-pends on the concentration of PEG and (NH4 )2 SO4 .A high extraction yield around 98% is achieved with the following parameters:(NH4)2SO4 15%,PEG2000 18%,pH 6.It is found that the extrac-tion yield undepends on the additional salt,but the presence of surfactant influences the extraction yield evidently.

  3. D-山梨醇与D-甘露醇在水和卤化钠水溶液中的稀释焓%Enthalpies of Dilution for D-sorbitol and D-mannitol in Pure Water and Aqueous Sodium Halide Solutions at 313.15K

    Institute of Scientific and Technical Information of China (English)

    宋明芝; 朱兰英; 王一蕾; 陈新萍; 孙德志

    2005-01-01

      应用流动式精密等温微量热技术,测定了互为旋光异构体的D-山梨醇和D-甘露醇在纯水与卤化钠水溶液中313.15K 下的稀释焓.根据 McMillan-Mayer 理论对所测数据进行关联,得到了稀释焓对浓度变化的经验方程和各阶焓相互作用系数h2、h3、h4.结果表明,在不同介质中,D-甘露醇和D-山梨醇在微观上的构象异构导致了一系列宏观上热力学性质上的差异.%  The enthalpies of dilution of D-sorbitol and D-mannitol, two optical isomers, with water and aqueous sodium halide solutions were determined by isothermal microcalorimetry at 313.15K. Experiental enthalpies of dilution varying with the concentration of the polylols were correlated with virial expansion equation, which was obtained with the McMillan-Mayer theory. Enthalpic interaction coefficients, h2, h3, h4, in the equations are got and the values of pair-wise enthalpic interaction coefficient (h2) have been discussed in terms of solute-solute and solute-solvent interactions and the different conformations of the two polylols.

  4. Sepiolite functionalized with N-[3-(trimethoxysilylpropyl]-ethylenediamine triacetic acid trisodium salt. Part II: Sorption of Ni2+ from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Lazarević Slavica S.

    2016-01-01

    Full Text Available sorption of Ni2+ on the sepiolite functionalized by covalent grafting of N-[3-(trimethoxysilylpropyl]ethylenediamine triacetic acid trisodium salt, MSEAS, was studied in batch experiments as a function of the initial metal concentration, the equilibration time, pH value, and temperature. The modification of sepiolite resulted in an enhanced Ni2+ retention with a capacity of 0.261 mmol/g at 298 K. The retention of Ni2+ ions occurred dominantly by specific sorption and exchange of Mg2+ ions from the sepiolite structure. The sorption process followed pseudo-second-order kinetics. The sorption equilibrium results were best described by the non-linear form of the Langmuir Sorption Equation. The values of the thermodynamic parameters (enthalpy, free energy and entropy were calculated from temperature dependent sorption isotherms and these values showed that the sorption of Ni2+ onto modified sepiolite was endothermic. [Projekat Ministarstva nauke Republike Srbije, br. III 45019 i FP7 NANOTECH FTM No. 245916

  5. "Switchable water": aqueous solutions of switchable ionic strength.

    Science.gov (United States)

    Mercer, Sean M; Jessop, Philip G

    2010-04-26

    "Salting out" is a standard method for separating water-soluble organic compounds from water. In this method, adding a large amount of salt to the aqueous solution forces the organic compound out of the aqueous phase. However, the method can not be considered sustainable because it creates highly salty water. A greener alternative would be a method that allows reversible salting out. Herein, we describe aqueous solutions of switchable ionic strength. Aqueous solutions of a diamine in water have essentially zero ionic strength but are converted by CO(2) into solutions of high ionic strength. The change is reversible. Application to the reversible salting out of THF from water is described.

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

    KAUST Repository

    Gurukar, Suresh Shivappa

    2015-08-17

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

  7. D-山梨醇在纯水和卤化钠水溶液中293.15K~318.15K的稀释焓%Enthalpies of Dilution of D-Sorbitol in Water and Sodium Halide Aqueous Solutions from 293. 15K to 318. 15K

    Institute of Scientific and Technical Information of China (English)

    宋明芝; 范传刚; 孙德志; 张在龙

    2011-01-01

    应用流动式等温精密微量热技术测定4个温度(293.15、303.15、308.15和318.15 K)下D-山梨醇在纯水和卤化钠水溶液中的稀释焓.根据改进的McMillan-Mayer理论对所测数据进行关联,得到了表观摩尔稀释焓对浓度变化的经验方程和各阶焓相互作用系数(h2,h3和h4)和二阶熵相互作用系数(s2),根据溶质-溶质、溶质-溶剂等弱相互作用对二阶焓、熵及吉布斯自由能相互作用系数进行了讨论,并探讨了温度对稀释焓的影响.结果表明,在山梨醇的纯水溶液和卤化钠水溶液中,其二阶焓相互作用系数h2随温度的升高而逐渐增大;不同温度下的二阶焓相互作用系数与温度成线性关系,因而二阶熵相互作用系数在实验温度范围内为一常量.%The enthalpies of dilution of D-sorbitol in water and sodium halide aqueous solutions had been determined by isothermal flow-mix microcalorimetry at 293. 15K, 303.15K, 308.15K, and 318. 15K. Experiential equations of apparent enthalpies of dilution varying with the concentration of D-sorbitol had been established from the experimental data in terms of the improved McMillan-Mayer theory, and enthalpic interaction coefficients (h2, h3, and h4 ), pairwise entropic interaction coefficient s2 and pairwise Gibbs free energy interaction coefficient g2 obtained. The values of h2 had been discussed in the light of solute-solute and solute-solvent interactions. The results indicated that,the values of h2 increased as raising temperature in pure water and the sodium halide aqueous solutions; and it shows quite well linear dependence on temperature, so s2 is a constant in the experimental range of temperature.

  8. A simple deep monitoring well dilution technique.

    Science.gov (United States)

    Rogiers, Bart; Labat, Serge; Gedeon, Matej; Vandersteen, Katrijn

    2015-04-01

    Well dilution techniques are well known and studied as one of the basic techniques to quantify groundwater fluxes. A typical well dilution test consists of the injection of a tracer, a mixing mechanism (e.g. water circulation with a pump) to achieve a homogeneous concentration distribution within the well, and monitoring of the evolution of tracer concentration with time. An apparent specific discharge can be obtained from such a test, and when details on the well construction are known, it can be converted into a specific discharge representative of the undisturbed aquifer. For deep wells however, the injection of tracer becomes less practical and the use of pumps for circulating and mixing the water becomes problematic. This is due to the limited pressure that common pumps can endure at the outlet, as well as the large volume of water that makes it difficult to achieve a homogeneous concentration, and the impracticalities of getting a lot of equipment to large depths in very small monitoring wells. Injection and monitoring of tracer at a specific depth omits several of the problems with deep wells. We present a very simple device that can be used to perform a dilution test at a specific depth in deep wells. The injection device consists of a PVC tube with a detachable rubber seal at its bottom. To minimize disturbance of the water column in the well, we integrated an EC sensor in this injection device, which enables us to use demineralized water or dissolved salts as a tracer. Once at the target depth, the PVC tube is retracted and the EC sensor and tracer become subject to groundwater flow. The device was tested on a shallow well, on which different types of dilution tests were performed. The results of the other tests agree well with the injection tube results. Finally, the device was used to perform a dilution test in a deep well in order to demonstrate the feasibility of the approach.

  9. Hydration of beryllium(II) in aqueous solutions of common inorganic salts. A combined vibrational spectroscopic and ab initio molecular orbital study.

    Science.gov (United States)

    Rudolph, Wolfram W; Fischer, Dieter; Irmer, Gert; Pye, Cory C

    2009-09-01

    Raman spectra of aqueous beryllium perchlorate, chloride, nitrate, and sulfate solutions have been measured over a broad concentration (0.098-4.950 mol L(-1)) range. The Raman spectroscopic data suggest that the tetra-aqua beryllium(II) ion is thermodynamically stable in perchlorate, chloride, and nitrate solutions over the concentration range measured. No inner-sphere complexes in these solutions could be detected spectroscopically except in very concentrated beryllium nitrate solutions. Beryllium sulfate solutions however, show a different picture, namely the existence of a thermodynamically stable beryllium sulfato complex most likely monodentate even at very low concentrations. At very high beryllium sulfate concentrations, a small quantity of a bidentate sulfato complex was found. With a temperature increase, the sulfato complex formation increases and this demonstrates the entropically driven sulfato complex formation. Furthermore, with increased temperature the hydrolysis increases, measured by the formation of hydrogen sulfate. Ab initio geometry optimizations and frequency calculations are reported for beryllium-water clusters with only inner sphere waters, clusters with an inner sphere and an incomplete second hydration, and clusters with a higher number of waters in the second hydration sphere. The cluster, [Be(OH2)(12)(2+)] (Be[4 + 8]) with 4 water molecules in the first sphere and 8 water molecules in the second sphere gave sufficiently realistic frequencies for BeO4 skeleton in comparison to the experimental ones. However, the cluster, [Be(OH2)(18)(2+)] (Be[6 + 12]) with 6 water molecules in the inner sphere and 12 water molecules in the outer sphere on an energy minimum gave unrealistically low BeO4 frequencies. This fact demonstrates that a six-fold coordination of Be2+ can be ruled out.

  10. Recovery of lignin peroxidase from submerged liquid fermentation of Amauroderma rugosum (Blume & T. Nees) Torrend using polyethylene glycol/salt aqueous two-phase system.

    Science.gov (United States)

    Jong, Wan Yng Linda; Show, Pau Loke; Ling, Tau Chuan; Tan, Yee Shin

    2017-07-01

    Amauroderma rugosum is a wild mushroom species widely distributed in tropics and is classified under the class of Basidiomycetes. Basidiomycetes are well-known for their abilities of producing lignocellulolytic enzymes such as lignin peroxidase (LiP), laccase (Lac) and manganese peroxidase (MnP). Different factors such as nutrient sources, incubation period and agitation affect the production of lignocellulolytic enzymes. The A. rugosum produced LiP in the medium supplemented with potato dextrose broth (PDB), 0.5% yeast and 1.0% saw dust at 26.70±3.31 U/mL. However, the LiP activity was increased to 106.32±5.32 U/mL when supplemented with 150 μm of copper (CuSO4). The aqueous two-phase system (ATPS) is a simple, rapid and low cost method for primary extraction and recovery of LiP. A total of 25 systems made from five different molecular weights of polyethylene glycol (PEG)/dipotassium hydrogen phosphate (K2HPO4) were tested. PEG 600 produced the highest top phase purification factor (PFT) of 1.33±0.62 with yield of 72.18±8.50%. The optimization of the ATPS parameters, such as volume ratio VR, pH and crude enzyme loading are the factors controlling the phase partition. Our results showed that significant improvement (PFT of 6.26±2.87 with yield of 87.31±3.14%) of LiP recovery can be achieved by optimized the parameters. Copyright © 2017 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.

  11. Quantitative analysis of aggregation in dilute solutions of effectively rigid biomacromolecules via the combination of oscillatory flow birefringence and viscoelasticity measurements: example study of aggregation of bovine fibrinogen in aqueous glycerol, and detection of a large aggregate formed on addition of guanidine hydrochloride.

    Science.gov (United States)

    Miller, J W; Nestler, F H M; Schrag, J L

    2004-12-20

    Oscillatory flow birefringence (OFB) properties have been measured for dilute solutions of bovine fibrinogen in 65-68% aqueous glycerol with the Miller-Schrag Thin Fluid Layer (TFL) apparatus employing either titanium or stainless steel surfaces in contact with the solutions. The shearing frequency range was 1 to 2500 Hz, the concentrations ranged from 4 to 8 mg/ml, and measurement temperatures were 9.9, 10.0, and 15.8 degrees C. The data showed evidence of significant amounts of aggregation that apparently is caused by the presence of glycerol; contributions from the various aggregates were readily detected since the staggered half-overlap aggregation in this system results in substantial differences in the rotational relaxation times of the various effectively rigid aggregates. The combination of oscillatory flow birefringence and viscoelasticity (VE) data provided sensitive and precise characterization of aggregation in these example systems; all aggregates exhibited the expected positive optical anisotropy. The length of unaggregated fibrinogen in solution was found to be that obtained via electron microscopy. Addition of guanidine hydrochloride to hopefully reduce aggregation did so but also resulted in formation of a very large (2800 to 3500 A), apparently nearly monodisperse, negatively birefringent aggregate, suggesting that this new species might be formed by lateral aggregation.

  12. Phase Behavior of Aqueous NA-K-MG-CA-CI-NO3 Mixtures: Isopiestic Measurements and Thermodynamic Modeling

    Energy Technology Data Exchange (ETDEWEB)

    M.S. Gruszkiewiez; D.A. Palmer; R.D. Springer; P. Wang; A. Anderko

    2006-09-14

    A comprehensive model has been established for calculating thermodynamic properties of multicomponent aqueous systems containing the Na{sup +}, K{sup +}, Mg{sup 2+}, Ca{sup 2+}, Cl{sup -}, and NO{sub 3}{sup -} ions. The thermodynamic framework is based on a previously developed model for mixed-solvent electrolyte solutions. The framework has been designed to reproduce the properties of salt solutions at temperatures ranging from the freezing point to 300 C and concentrations ranging from infinite dilution to the fused salt limit. The model has been parameterized using a combination of an extensive literature database and new isopiestic measurements for thirteen salt mixtures at 140 C. The measurements have been performed using Oak Ridge National Laboratory's (ORNL) previously designed gravimetric isopiestic apparatus, which makes it possible to detect solid phase precipitation. Water activities are reported for mixtures with a fixed ratio of salts as a function of the total apparent salt mole fraction. The isopiestic measurements reported here simultaneously reflect two fundamental properties of the system, i.e., the activity of water as a function of solution concentration and the occurrence of solid-liquid transitions. The thermodynamic model accurately reproduces the new isopiestic data as well as literature data for binary, ternary and higher-order subsystems. Because of its high accuracy in calculating vapor-liquid and solid-liquid equilibria, the model is suitable for studying deliquescence behavior of multicomponent salt systems.

  13. Coordination chemistry in fused-salt solutions

    Science.gov (United States)

    Gruen, D. M.

    1969-01-01

    Spectrophotometric work on structural determinations with fused-salt solutions is reviewed. Constraints placed on the method, as well as interpretation of the spectra, are discussed with parallels drawn to aqueous spectrophotometric curves of the same materials.

  14. Self-assembly of aqueous bilirubin ditaurate, a natural conjugated bile pigment, to contraposing enantiomeric dimers and M(-) and P(+) tetramers and their selective hydrophilic disaggregation by monomers and micelles of bile salts.

    Science.gov (United States)

    Neubrand, Michael W; Carey, Martin C; Laue, Thomas M

    2015-02-24

    The solution behavior of bilirubin ditaurate (BDT), the first naturally occurring conjugated bile pigment to be physically and chemically characterized, was assessed in aqueous solution and in monomeric and micellar solutions of common taurine-conjugated bile salts (BS). Analytical ultracentrifugation revealed that BDT self-associates in monomer-dimer equilibria between 1 and 500 μM, forming limiting tetramers at low millimolar concentrations. Self-association was enthalpically driven with ΔG values of ≈5 kcal/mol, suggesting strong hydrophobic interactions. Added NaCl and decreases in temperature shifted the oligomerization to lower BDT concentrations. On the basis of circular dichroism spectra and the limiting size of the self-aggregates, we infer that the tetramers are composed of 2P(+) and 2M(-) enantiomeric BDT pairs in "ridge-tile" conformations interacting in a "double-bookend" structure. With added monomeric BS, blue shifts in the UV-vis spectra and tight isosbestic points revealed that BDT/BS heterodimers form, followed by BDT "decorating" BS micelles mostly via hydrophilic interactions. Conformational enantiomerism, fluorescence intensities, and anisotropy, as well as resistance of the hybrid particles to disaggregation in 6 M urea, suggested that two or three hydrogen-bonding sites bound BDT monomers to the hydroxyl groups of BS, possibly via pyrrole-π-orbital-OH interactions. BDT stabilized these interactions by enveloping the BS in its "ridge-tile" pincers with variable strain that maximized van der Waals interactions. Possibly because the BDT molecule becomes highly strained with BS subtending a 7β-hydroxyl group, BDT became totally resistant to oxidation in air. This work predicts that, because of BS dissolution of the BDT self-aggregates, BS/bilirubin hybrid particles, which are stabilized hydrophilically, are likely to be the dominant mode of transport for all conjugated bilirubins in bile.

  15. ANALYSIS OF VISCOSITY ABNORMALITIES OF POLYELECTROLYTES IN DILUTE SOLUTIONS

    Institute of Scientific and Technical Information of China (English)

    Jian-qiang Chen; Yu-fang Shao; Zhen Yang; Hu Yang; Rong-shi Cheng

    2011-01-01

    It was found that the interface effects in viscous capillary flow influenced the process of viscosity measurement greatly,and the abnormal viscosity behaviors of polyelectrolytes as well as neutral polymers in dilute solution region were ascribed to interface effect.According to this theory,we have reviewed the previous viscosity data of derivatives of poly-2-vinylpyridine reported by Maclay and Fuoss first.Then,the abnormal viscosity behaviors of a series of sodium polystyrene sulfonate samples with various molecular weights in dilute aqueous solutions were studied further.The solute adsorption behaviors and structural information of polymers have been discussed carefully.

  16. Frost formation with salt

    Science.gov (United States)

    Guadarrama-Cetina, J.; Mongruel, A.; González-Viñas, W.; Beysens, D.

    2015-06-01

    The formation of frost in presence of salt (NaCl) crystal is experimentally investigated on a hydrophobic surface. It presents several remarkable features due to the interplay of salty-water saturation pressure evolution, initially lower than the saturation pressure of ice and water, and the percolating propagation of ice dendrites from defects throughout the supercooled water droplet pattern. In particular, it is remarkable that nucleation of supercooled water and/or ice is prevented around the salty drop in a region of inhibited condensation where the substrate remains dry. As condensation proceeds, salt concentration decreases to eventually become lower than ice's, allowing ice dendrites to hit the salty drop. Salty water then melts ice but eventually freezes as an effect of dilution.

  17. Dilution thermodynamics of the biologically relevant cation mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Kaczyński, Marek, E-mail: marek.kaczynski@pwr.wroc.pl; Borowik, Tomasz, E-mail: office@novel-id.pl; Przybyło, Magda, E-mail: magdalena.przybylo@pwr.wroc.pl; Langner, Marek, E-mail: marek.langner@pwr.wroc.pl

    2014-01-10

    Graphical abstract: - Highlights: • Dilution energetics of Ca{sup 2+} can be altered by the aqueous phase ionic composition. • Dissipated heat upon Ca{sup 2+} dilution is drastically reduced in the K{sup +} presence. • Reduction of the enthalpy change upon Ca{sup 2+} dilution is K{sup +} concentration dependent. • The cooperativity of Ca{sup 2+} hydration might be of great biological relevance providing a thermodynamic argument for the specific ionic composition of the intracellular environment. - Abstract: The ionic composition of intracellular space is rigorously controlled by a variety of processes consuming large quantities of energy. Since the energetic efficiency is an important evolutional criterion, therefore the ion fluxes within the cell should be optimized with respect to the accompanying energy consumption. In the paper we present the experimental evidence that the dilution enthalpies of the biologically relevant ions; i.e. calcium and magnesium depend on the presence of monovalent cations; i.e. sodium and potassium. The heat flow generated during the dilution of ionic mixtures was measured with the isothermal titration calorimetry. When calcium was diluted together with potassium the dilution enthalpy was drastically reduced as the function of the potassium concentration present in the solution. No such effect was observed when the potassium ions were substituted with sodium ones. When the dilution of magnesium was investigated the dependence of the dilution enthalpy on the accompanying monovalent cation was much weaker. In order to interpret experimental evidences the ionic cluster formation is postulated. The specific organization of such cluster should depend on ions charges, sizes and organization of the hydration layers.

  18. Radiation induced degradation of ketoprofen in dilute aqueous solution

    Science.gov (United States)

    Illés, Erzsébet; Takács, Erzsébet; Dombi, András; Gajda-Schrantz, Krisztina; Gonter, Katalin; Wojnárovits, László

    2012-09-01

    The intermediates and final products of ketoprofen degradation were investigated in 0.4 mmol dm-3 solution by pulse radiolysis and gamma radiolysis. For observation of final products UV-vis spectrophotometry and HPLC separation with diode array detection were used, and for identification MS was used. The reactions of •OH lead to hydroxycyclohexadienyl type radical intermediates, in their further reactions hydroxylated derivatives of ketoprofen form as final products. The hydrated electron is scavenged by the carbonyl oxygen and the electron adduct protonates to ketyl radical •OH is more effective in decomposing ketoprofen than hydrated electron. Chemical oxygen demand and total organic carbon content measurements on irradiated aerated solutions showed that using irradiation technology ketoprofen can be mineralised. The initial toxicity of the solution monitored by the Daphnia magna test steadily decreases with irradiation. Using 5 kGy dose no toxicity of the solution was detected with this test.

  19. Thermal decomposition of dilute aqueous formic acid solutions

    DEFF Research Database (Denmark)

    Bjerre, A.B.; Sørensen, E.

    1992-01-01

    or a decarboxylation. In particular the second one is dependent on the reactor vessel used. It is shown to be catalyzed by a mixture of oxides of stainless steel components. The presence of CH3COOH or CH3CHO promotes the decomposition of HCOOH by way of both decarboxylation and oxidation. In any case formic acid...

  20. Enrichment of surfactant from its aqueous solution using ultrasonic atomization.

    Science.gov (United States)

    Takaya, Haruko; Nii, Susumu; Kawaizumi, Fumio; Takahashi, Katsuroku

    2005-08-01

    Dilute aqueous solutions of dodecyl-benzenesulfonic acid sodium salt (DBS-Na) and polyoxyethylenenonylphenyl ethers (PONPEs) were ultrasonically atomized. The surfactants were concentrated in collected mist droplets. The enrichment ratio increased with decreasing surfactant concentration. Depending on the surfactant's molecular weight and affinity to water, different enrichment ratio was observed in the range of low feed concentrations. For anionic surfactant, DBS-Na, the enrichment ratio was significantly improved by KCl addition and a peak appeared on the plot of the ratio against KCl concentration. Addition of NaCl or CaCl2 . 2H2O to the surfactant solution also enhanced the enrichment ratio; however, the effect was relatively small. Such behaviors of the ratio were interpreted as enhanced interfacial adsorption of the surfactant and a lack of supply of surfactant monomers from liquid bulk because of slow breaking of surfactant micelles. Time required for collecting an amount of mist was also observed. Among the three salt systems, the time for KCl system was twice as long as others. This fact suggested that the formation of smaller droplets in KCl system.

  1. A computational approach to calculate the heat of transport of aqueous solutions

    Science.gov (United States)

    Di Lecce, Silvia; Albrecht, Tim; Bresme, Fernando

    2017-01-01

    Thermal gradients induce concentration gradients in alkali halide solutions, and the salt migrates towards hot or cold regions depending on the average temperature of the solution. This effect has been interpreted using the heat of transport, which provides a route to rationalize thermophoretic phenomena. Early theories provide estimates of the heat of transport at infinite dilution. These values are used to interpret thermodiffusion (Soret) and thermoelectric (Seebeck) effects. However, accessing heats of transport of individual ions at finite concentration remains an outstanding question both theoretically and experimentally. Here we discuss a computational approach to calculate heats of transport of aqueous solutions at finite concentrations, and apply our method to study lithium chloride solutions at concentrations >0.5 M. The heats of transport are significantly different for Li+ and Cl− ions, unlike what is expected at infinite dilution. We find theoretical evidence for the existence of minima in the Soret coefficient of LiCl, where the magnitude of the heat of transport is maximized. The Seebeck coefficient obtained from the ionic heats of transport varies significantly with temperature and concentration. We identify thermodynamic conditions leading to a maximization of the thermoelectric response of aqueous solutions.

  2. Electrolytic orthoborate salts for lithium batteries

    Science.gov (United States)

    Angell, Charles Austen; Xu, Wu

    2008-01-01

    Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

  3. 基于多级蒸汽机械再压缩热泵的稀N,N-二甲基甲酰胺水溶液蒸馏浓缩工艺%Distillation Concentration of Dilute Dimethylformamide Aqueous Solution Based on Multi-Stage Mechanical Vapor Recompression Heat Pump

    Institute of Scientific and Technical Information of China (English)

    杨德明; 陶磊

    2012-01-01

    A process for triple-stage mechanical vapor recompression(MVR) heat pump concentration, which was applied to treating dilute dimethylformamide aqueous solution, was presented by the analysis of the characters and working conditions of the MVR heat pump concentration technique. Aimed at the minimum of the energy consumption, the triple-stage MVR heat pump concentration and triple effect concentration were simulated by means of Compr module and Radfrac module of Aspen Plus software, and suitable parameters were obtained. The research results showed that the triple-stage MVR heat pump concentration process could save energy by 83.2% compared with the triple effect concentration, and the average COP(cofficient of performance) reached 0.834.%分析了蒸汽机械再压缩(MVR)热泵蒸馏浓缩工艺的特点和适用工况,以稀N,N-二甲基甲酰胺水溶液的浓缩过程为研究对象,提出了三级MVR热泵蒸馏浓缩工艺.采用Aspen Plus化工流程模拟软件中的严格精馏模块和压缩机模块,以能耗最低为目标函数,对三级MVR热泵蒸馏浓缩工艺和三效蒸馏浓缩工艺分别进行了模拟与优化,得到了合适的工艺操作参数.模拟结果表明,与三效蒸馏浓缩工艺相比,三级MVR热泵蒸馏浓缩工艺节能约83.2%,其平均能效比(压缩机制热量与压缩机输入功率的比)为0.834;多级MVR热泵蒸馏浓缩工艺具有较大的经济优势.

  4. Supramolecular Complexes Formed in Systems Bile Salt-Bilirubin-Silica

    Science.gov (United States)

    Vlasova, N. N.; Severinovskaya, O. V.; Golovkova, L. P.

    The formation of supramolecular complexes between bilirubin and primary micelles of bile salts has been studied. The association constants of bile salts and binding of bilirubin with these associates have been determined. The adsorption of bilirubin and bile salts from individual and mixed aqueous solutions onto hydrophobic silica surfaces has been investigated. The interaction of bilirubin with primary bile salt micelles and the strong retention in mixed micelles, which are supramolecular complexes, result in the adsorption of bilirubin in free state only.

  5. Acetic acid extraction from aqueous solutions using fatty acids

    NARCIS (Netherlands)

    IJmker, H.M.; Gramblicka, M.; Kersten, Sascha R.A.; van der Ham, Aloysius G.J.; Schuur, Boelo

    2014-01-01

    A major challenge for production of acetic acid via bio-based routes is cost-effective concentration and purification of the acetic acid from the aqueous solutions, for which liquid–liquid extraction is a possible method. A main challenge in extraction of acetic acid from dilute aqueous solutions is

  6. Acetic acid extraction from aqueous solutions using fatty acids

    NARCIS (Netherlands)

    IJmker, H.M.; Gramblicka, M.; Kersten, S.R.A.; Ham, van der A.G.J.; Schuur, B.

    2014-01-01

    A major challenge for production of acetic acid via bio-based routes is cost-effective concentration and purification of the acetic acid from the aqueous solutions, for which liquid–liquid extraction is a possible method. A main challenge in extraction of acetic acid from dilute aqueous solutions is

  7. Phosphate salts

    Science.gov (United States)

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

  8. Salt cookbook

    CERN Document Server

    Saha, Anirban

    2015-01-01

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

  9. General electrokinetic model for concentrated suspensions in aqueous electrolyte solutions: Electrophoretic mobility and electrical conductivity in static electric fields.

    Science.gov (United States)

    Carrique, Félix; Ruiz-Reina, Emilio; Roa, Rafael; Arroyo, Francisco J; Delgado, Ángel V

    2015-10-01

    In recent years different electrokinetic cell models for concentrated colloidal suspensions in aqueous electrolyte solutions have been developed. They share some of its premises with the standard electrokinetic model for dilute colloidal suspensions, in particular, neglecting both the specific role of the so-called added counterions (i.e., those released by the particles to the solution as they get charged), and the realistic chemistry of the aqueous solution on such electrokinetic phenomena as electrophoresis and electrical conductivity. These assumptions, while having been accepted for dilute conditions (volume fractions of solids well below 1%, say), are now questioned when dealing with concentrated suspensions. In this work, we present a general electrokinetic cell model for such kind of systems, including the mentioned effects, and we also carry out a comparative study with the standard treatment (the standard solution only contains the ions that one purposely adds, without ionic contributions from particle charging or water chemistry). We also consider an intermediate model that neglects the realistic aqueous chemistry of the solution but accounts for the correct contribution of the added counterions. The results show the limits of applicability of the classical assumptions and allow one to better understand the relative role of the added counterions and ions stemming from the electrolyte in a realistic aqueous solution, on electrokinetic properties. For example, at low salt concentrations the realistic effects of the aqueous solution are the dominant ones, while as salt concentration is increased, it is this that progressively takes the control of the electrokinetic response for low to moderate volume fractions. As expected, if the solids concentration is high enough the added counterions will play the dominant role (more important the higher the particle surface charge), no matter the salt concentration if it is not too high. We hope this work can help in

  10. Effects of Ultra-Highly Diluted Solutions of Palicourea marcgravii St. Hill in Rats Poisoned by Aqueous Extracts of This Plant Efectos de altas diluciones de Palicourea marcgravii St Hill en ratones intoxicados con extracto acuoso de esta planta Efeitos de altas diluições de Palicourea marcgravii St Hill em ratos intoxicados com extrato aquoso dessa planta.

    Directory of Open Access Journals (Sweden)

    Luiz Figueira Pinto

    2008-12-01

    Full Text Available

     Palicourea marcgravii , a shrub causing sudden death in cattle, is a major cause of economic loss to breeders in Brazil. The aim of the present study was to evaluate the effects of high diluted solutions  6cH and 30cH of P. marcgravii, on the development of tolerance to the toxic effects of this plant. 14 adult Wistar rats were divided into 3 test groups. AE group was composed of 4 rats receiving  aqueous extract of P. marcgravii intragastrically at a dose of 2g/kg. Groups HD6AE and HD30AE comprised 5 rats each. Animals in these groups received 1 mL of 6cH and 30cH solutions of P. marcgravii respectively by oral route 3 times a day, for 8 days. At the end of this period, they were intragastrically intoxicated with 2g/kg   of aqueous extract of P. marcgravii,  receiving the corresponding high diluted preparation hourly until death. MainRemoval of Phenol from Dilute Solutions by Predispersed Solvent Extraction

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Predispersed solvent extraction (PDSE) is a new method for separating solutes from aqueous solution by solvent extraction and one which has shown promise for extraction from extremely dilute solution very efficient and very quick. The use of colloidal liquid aphrons in predispersed solvent extraction may ameliorate the problems such as emulsion formation, reduction of interfacial mass transfer and low interfacial mass transfer areas in solvent extraction process. In present paper, colloidal liquid aphrons are successfully generated using kerosene as a solvent, tributyl phosphate(TBP) as an extractant, sodium dodecyl benzene sulphate(SDBS) as surfactant in aqueous phase and Tween-80 in oil phase. Extraction of phenol from dilute solution was studied by using colloidal liquid aphrons and colloidal gas aphrons in a semi-batch extraction column. It has been found that the PDSE process is more suitable for extraction of dilute solutions. It has also been discovered that the PDSE process has a great advantage over traditional single-stage extraction process.

  11. Recovery of nickel from aqueous solutions by complexation-ultrafiltration process with sodium polyacrylate and polyethylenimine.

    Science.gov (United States)

    Shao, Jiahui; Qin, Shu; Davidson, Joshua; Li, Wenxi; He, Yiliang; Zhou, H Susan

    2013-01-15

    The recovery of nickel from aqueous dilute solutions by complexation-ultrafiltration process with sodium polyacrylate (PAAS) and polyethylenimine (PEI) was studied. Experiments were performed as a function of aqueous pH, polymer/Ni(2+) ratio and background electrolyte concentration. At optimum experimental conditions, the nickel removal rate reaches 99.5% using PAAS and 93.0% using PEI as the complexation agent. The nickel removal rate was found to decrease as the adding salt NaCl concentration increases for both complexation agents. A series of experiments implied that the mechanism could be the compressing electric double layer other than the competitive complexation. Diafiltration technique was further performed to regenerate complexation agents and recover nickel. The nickel removal rates were found to be close to those obtained with the original PEI and PAAS. Finally, Langmuir-type binding isotherm equation was employed to evaluate the extent of nickel bound to PAAS and PEI. The overall results from the two-step process of complexation-UF and decomplexation-UF separation showed that it could be a promising method for nickel removal and recovery from aqueous solutions.

  12. Sorption of water vapor, hydration, and viscosity of carboxymethylhydroxypropyl guar, diutan, and xanthan gums, and their molecular association with and without salts (NaCl, CaCl2, HCOOK, CH3COONa, (NH4)2SO4 and MgSO4) in aqueous solution.

    Science.gov (United States)

    Banerjee, Paltu; Mukherjee, Indrajyoti; Bhattacharya, Subhash; Datta, Sidhhartha; Moulik, Satya P; Sarkar, Diptabhas

    2009-10-06

    Gums are routinely used in food industry, pharmacy and oil recovery process. In these uses, the hydrocolloids very often encounter interactions with salts at moderate to high temperature. Since they are normally employed in the form of solution and gel, their viscous or fluidity properties need detailed investigation. In the present work, properties such as water vapor adsorption of finely powdered carboxymethylhydroxypropyl derivatized guar (CMHPG) as well as xanthan (Xn) and diutan (Dn) gums, their hydration in solution, their viscosity behaviors, and salt effects on fluidity have been studied. The concentration domains for the existence of free and associated molecules in the studied solutions have been assessed from the viscosity results. The gums have been found to bind a fair amount of water from the vapor phase with them. In solution, they can interact and arrest a large amount of water in their folded configuration. Intrinsic viscosities of the gums in aqueous medium declined in the presence of salts. The activation energies for their viscous flow were moderate and comparable, and were dependent on their concentrations. From the power law relation and viscosity master curve behavior mostly two critical association states of the macromolecular dispersions were envisaged.

  13. (II) and Pb (II) ions from aqueous media using Sta

    African Journals Online (AJOL)

    Joshua Konne

    Removal of Ni (II), Co (II) and Pb (II) ions from aqueous media using Starch. Stabilized Magnetic ... initial metal concentration and contact time on the removal processes was investigated. The results .... India) supplied NaOH and the Fe salts.

  14. Trace determination of zinc by substoichiometric isotope dilution analysis

    Energy Technology Data Exchange (ETDEWEB)

    Sandhya, D.; Priya, S.; Subramanian, M.O.S. [Indian Institute of Technology, Madras (India)

    1996-09-01

    A radiometric method based on substoichiometric isotope dilution analysis using 1,10-phenanthroline and a substoichiometric amount of eosin was developed for determining trace amounts of zinc. Evaluation of various metal ion interferences shows that as little as 0.2 {mu}g Zn could be determined in an aqueous-phase volume of 60 mL. The method has been successfully applied to the determination of Zn in city waste incineration ash, cadmium metal, Fourts-B tablets, Boro-plus ointment, and magnesium alloy samples. 12 refs., 3 figs., 3 tabs.

  15. An Isotopic Dilution Experiment Using Liquid Scintillation: A Simple Two-System, Two-Phase Analysis.

    Science.gov (United States)

    Moehs, Peter J.; Levine, Samuel

    1982-01-01

    A simple isotonic, dilution analysis whose principles apply to methods of more complex radioanalyses is described. Suitable for clinical and instrumental analysis chemistry students, experimental manipulations are kept to a minimum involving only aqueous extraction before counting. Background information, procedures, and results are discussed.…

  16. Metal separations using aqueous biphasic partitioning systems

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, D.J.; Zaslavsky, B.; Rollins, A.N.; Vojta, Y.; Gartelmann, J.; Mego, W. [Argonne National Lab., IL (United States). Chemical Technology Div.

    1996-05-01

    Aqueous biphasic extraction (ABE) processes offer the potential for low-cost, highly selective separations. This countercurrent extraction technique involves selective partitioning of either dissolved solutes or ultrafine particulates between two immiscible aqueous phases. The extraction systems that the authors have studied are generated by combining an aqueous salt solution with an aqueous polymer solution. They have examined a wide range of applications for ABE, including the treatment of solid and liquid nuclear wastes, decontamination of soils, and processing of mineral ores. They have also conducted fundamental studies of solution microstructure using small angle neutron scattering (SANS). In this report they review the physicochemical fundamentals of aqueous biphase formation and discuss the development and scaleup of ABE processes for environmental remediation.

  17. Boiling heat transfer in dilute emulsions

    CERN Document Server

    Roesle, Matthew Lind

    2013-01-01

    Boiling Heat Transfer in Dilute Emulsions synthesizes recent advances and established understanding on the subject of boiling in dilute emulsions. Experimental results from various sources are collected and analyzed, including contemporary experiments that correlate visualization with heat transfer data. Published models of boiling heat transfer in dilute emulsions, and their implementation, are described and assessed against experimental data.

  18. Phase equilibria for salt-induced lysozyme precipitation: Effect of salt concentration and pH

    OpenAIRE

    Popova, E.; WATANABE, E. O.; PESSOA FILHO, P. A.; Maurer, G.

    2008-01-01

    The salt-induced precipitation of lysozyme from aqueous solutions was studied at 25 degrees C and various pH values by cloud-point investigations, precipitation experiments (analysing the compositions of the coexisting phases) and microscopic investigations of the precipitates. Sodium sulphate as well as ammonium sulphate were used to induce the precipitation. The experimental results are discussed and used to develop a scheme of the phase equilibrium in water-rich aqueous solutions of lysozy...

  19. Turbulence in dilute polymer solutions

    Science.gov (United States)

    Liberzon, A.; Guala, M.; Lüthi, B.; Kinzelbach, W.; Tsinober, A.

    2005-03-01

    The work reported below is a comparative study of the properties of turbulence with weak mean flow in a Newtonian fluid and in a dilute polymer solution with an emphasis on the small scale phenomena. The main tool used is a three-dimensional particle tracking system allowing to measure and follow in a Lagrangian manner the field of velocities, as well as velocity derivatives, and thus vorticity, strain, and a variety of related and dynamically significant quantities. The comparison of data from the two flows allows to directly observe the influence of polymers on these quantities as well as the evolution of material elements in the presence of polymers.

  1. Thermodynamic properties of potassium chloride aqueous solutions

    Science.gov (United States)

    Zezin, Denis; Driesner, Thomas

    2017-04-01

    Potassium chloride is a ubiquitous salt in natural fluids, being the second most abundant dissolved salt in many geological aqueous solutions after sodium chloride. It is a simple solute and strong electrolyte easily dissociating in water, however the thermodynamic properties of KCl aqueous solutions were never correlated with sufficient accuracy for a wide range of physicochemical conditions. In this communication we propose a set of parameters for a Pitzer-type model which allows calculation of all necessary thermodynamic properties of KCl solution, namely excess Gibbs free energy and derived activity coefficient, apparent molar enthalpy, heat capacity and volume, as well as osmotic coefficient and activity of water in solutions. The system KCl-water is one of the best studied aqueous systems containing electrolytes. Although extensive experimental data were collected for thermodynamic properties of these solutions over the years, the accurate volumetric data became available only recently, thus making possible a complete thermodynamic formulation including a pressure dependence of excess Gibbs free energy and derived properties of the KCl-water liquids. Our proposed model is intended for calculation of major thermodynamic properties of KCl aqueous solutions at temperatures ranging from freezing point of a solution to 623 K, pressures ranging from saturated water vapor up to 150 MPa, and concentrations up to the salt saturation. This parameterized model will be further implemented in geochemical software packages and can facilitate the calculation of aqueous equilibrium for reactive transport codes.

  2. Influence of Salts on the Partitioning of 5-Hydroxymethylfurfural in Water/MIBK.

    Science.gov (United States)

    Mohammad, Sultan; Held, Christoph; Altuntepe, Emrah; Köse, Tülay; Sadowski, Gabriele

    2016-04-28

    This study investigates the influence of electrolytes on the performance of extracting 5-hydroxymethylfurfural (HMF) from aqueous media using methyl isobutyl ketone (MIBK). For that purpose, liquid-liquid phase equilibria (LLE) of quaternary systems containing HMF, water, MIBK and salts were measured at atmospheric pressure and 298.15 K. The salts under investigation were composed of one of the anions NO(3-), SO4(2-), Cl(-), or CH3COO(-) and of one of the alkali cations Li(+), Na(+), or K(+). On the basis of these LLE data, the partition coefficient of HMF between the aqueous and the MIBK phase KHMF was determined. It could be shown that KHMF significantly depends on the kind and concentration of the added salt. Weak electrolytes (e.g., sulfates, acetates) caused salting-out, whereas nitrates caused salting-in of HMF to the aqueous phase. Unexpectedly, LiCl caused salting-out at low LiCl concentrations and salting-in at LiCl concentrations higher than 3 mol/kgH2O. The model electrolyte perturbed-chain SAFT (ePC-SAFT) was used to predict the salt influence on the LLE in the quaternary systems water/MIBK/HMF/salt in good agreement with the experimental data. On the basis of ePC-SAFT, it could be concluded that the different salting-out/salting-in behavior of the various salts is mainly caused by their different tendency to form ion pairs in aqueous solutions.

  3. Dilute Acid and Autohydrolysis Pretreatment

    Science.gov (United States)

    Yang, Bin; Wyman, Charles E.

    Exposure of cellulosic biomass to temperatures of about 120-210°C can remove most of the hemicellulose and produce cellulose-rich solids from which high glucose yields are possible with cellulase enzymes. Furthermore, the use of dilute sulfuric acid in this pretreatment operation can increase recovery of hemicellulose sugars substantially to about 85-95% of the maximum possible versus only about 65% if no acid is employed. The use of small-diameter tubes makes it possible to employ high solids concentrations similar to those preferred for commercial operations, with rapid heat-up, good temperature control, and accurate closure of material balances. Mixed reactors can be employed to pretreat larger amounts of biomass than possible in such small-diameter tubes, but solids concentrations are limited to about 15% or less to provide uniform temperatures. Pretreatment of large amounts of biomass at high solids concentrations is best carried out using direct steam injection and rapid pressure release, but closure of material balances in such “steam gun” devices is more difficult. Although flow of water alone or containing dilute acid is not practical commercially, such flow-through configurations provide valuable insight into biomass deconstruction kinetics not possible in the batch tubes, mixed reactors, or steam gun systems.

  4. Extraction of endo-pectinase activity from the culture filtrate of Polyporus squamosus by aqueous two-phase systems composed of low molecular mass polyethylene glycol and phosphate salt

    Directory of Open Access Journals (Sweden)

    Peričin Draginja M.

    2004-01-01

    Full Text Available Separation of endo-pectinase activity from the culture filtrate of Polyporus squamosus - strain MMOL76, by aqueous two-phase partitioning technique in polyethylene glycol/sodium dihydrogen phosphate system was investigated as the first operation in the downstream processing of enzyme. The best results concerning the partitioning coefficient and the top phase yield were achieved in the polyethylene glycol 400/sodium dihydrogen phosphate system at the tie-line length 78.9 % at pH 3.8 (K = 8, with a 90% yield.

  5. Centrifugal separation for miscible solutions: Fundamentals and applications to separation of molten salt nuclear material

    Science.gov (United States)

    Li, Ning; Camassa, Roberto; Ecke, Robert E.; Venneri, Francesco

    1995-09-01

    We report on the physical separation of dilute solutions using centrifugal techniques. We use numerical simulations of the diffusion and sedimentation dynamics of centrifugation to model the approach to an equilibrium concentration profile. We verify experimentally the equilibrium profiles for aqueous solutions of different salts under rotation at 25000 rpm corresponding to centrifugal accelerations of about 57,000 g and 75,000 g in two different commercial centrifuges. These measurements provide ratios of sedimentation and diffusion coefficients. We show experimental results for the dynamics of separation that confirm the predictions of the theoretical model. We also measure the mass diffusion coefficient for several solutions. Although the relaxation to equilibrium is long, we have determined a method for efficiently extracting enriched components from a ternary mixture based on fast dynamics at early times. These dynamics are modeled in numerical simulations with realistic fluid parameters. Based on these studies we show that a multistage centrifugal separation process could provide efficient physical separation of actinides and fission products from a molten-salt solution in proposed transmutation/energy-production systems. We consider technical issues in the design of such a separation system.

  6. Tank 29 salt removal method using slurry pump agitation

    Energy Technology Data Exchange (ETDEWEB)

    Parish, W.R.

    1993-11-30

    This report outlines a plan for removing salt from Tank 29. The plan is based, in part, upon the experience gained in the removal of salt from Tank 19 and sludge from Tank 16. Tank 19 was the first tank in which slurry pumps were used during salt dissolution. Salt in Tank 29 will be dissolved to form a nearly saturated salt solution. The goal of Waste Removal is to remove the salt from the tank and deliver it to In-Tank Precipitation (ITP) at a concentration greater than 6.7 molar Na{sup +} (including dilution from transfer steam) to meet ITP requirements. (The amount of wash water used in ITP will be enough to dilute 6.7 molar Na{sup +} salt solution to 5 molar Na{sup +} required for the precipitation step). The solution will be sent to (ITP) for precipitation of soluble cesium and strontium (radioactive elements). The precipitate will be transferred to the Defense Waste Processing Facility (DWPF) for final disposal. A USQD (Unreviewed Safety Question Determination) for criticality safety issue resolution will be completed prior to salt removal.

  7. AQUEOUS BIPHASE EXTRACTION FOR PROCESSING OF FINE COAL

    Energy Technology Data Exchange (ETDEWEB)

    K. Osseo-Asare; X. Zeng

    2002-01-01

    The objective of this research project is to develop an aqueous biphase extraction process for the treatment of fine coals. Aqueous biphase extraction is an advanced separation technology that relies on the ability of an aqueous system consisting of a water-soluble polymer and another component, e.g., another polymer, an inorganic salt, or a nonionic surfactant, to separate into two immiscible aqueous phases. The principle behind the partition of solid particles in aqueous biphase systems is the physicochemical interaction between the solid surface and the surrounding liquid solution. In order to remove sulfur and mineral matter from fine coal with aqueous biphasic extraction, it is necessary to know the partitioning behavior of coal, as well as the inorganic mineral components. Therefore, in this research emphasis was placed on the partitioning behavior of fine coal particles as well as model fine inorganic particles in aqueous biphase systems.

  8. New absorption liquids for the removal of CO2 from dilute gas streams using membrane contactors

    NARCIS (Netherlands)

    Kumar, P.S.; Hogendoorn, J.A.; Feron, P.H.M.; Versteeg, G.F.

    2002-01-01

    A new absorption liquid based on amino acid salts has been studied for CO2 removal in membrane gas-liquid contractors. Unlike conventional gas treating solvents like aqueous alkanolamines solutions, the new absorption liquid does not wet polyolefin microporous membranes. The wetting characteristics

  9. Flow of Aqueous Humor

    Science.gov (United States)

    ... Home Flow of Aqueous Humor Flow of Aqueous Humor Most, but not all, forms of glaucoma are ... remains normal when some of the fluid (aqueous humor) produced by the eye's ciliary body flows out ...

  10. Synergy of boric acid and added salts in the catalytic dehydration of hexoses to 5-hydroxymethylfurfural in water

    DEFF Research Database (Denmark)

    Hansen, Thomas Steen; Mielby, Jerrik Jørgen; Riisager, Anders

    2011-01-01

    Boric acid and salts showed a synergistic effect on the dehydration of concentrated aqueous sugar solutions to yield 5-hydroxymethylfurfural.......Boric acid and salts showed a synergistic effect on the dehydration of concentrated aqueous sugar solutions to yield 5-hydroxymethylfurfural....

  11. Turbulence of Dilute Polymer Solution

    CERN Document Server

    Xi, Heng-Dong; Xu, Haitao

    2013-01-01

    In fully developed three dimensional fluid turbulence the fluctuating energy is supplied at large scales, cascades through intermediate scales, and dissipates at small scales. It is the hallmark of turbulence that for intermediate scales, in the so called inertial range, the average energy flux is constant and independent of viscosity [1-3]. One very important question is how this range is altered, when an additional agent that can also transport energy is added to the fluid. Long-chain polymers dissolved at very small concentrations in the fluid are such an agent [4,5]. Based on prior work by de Gennes and Tabor [6,7] we introduce a theory that balances the energy flux through the turbulent cascade with that of the energy flux into the elastic degrees of freedom of the dilute long-chain polymer solution. We propose a refined elastic length scale, $r_\\varepsilon$, which describes the effect of polymer elasticity on the turbulence energy cascade. Our experimental results agree excellently with this new energy ...

  12. Chemical reactions at aqueous interfaces

    Science.gov (United States)

    Vecitis, Chad David

    2009-12-01

    ) Adsorption of dilute PFOS(aq) and PFOA(aq) to acoustically cavitating bubble interfaces was greater than equilibrium expectations due to high-velocity bubble radial oscillations; 2) Relative ozone oxidation kinetics of aqueous iodide, sulfite, and thiosulfate were at variance with previously reported bulk aqueous kinetics; 3) Organics that directly chelated with the anode surface were oxidized by direct electron transfer, resulting in immediate carbon dioxide production but slower overall oxidation kinetics. Chemical reactions at aqueous interfaces can be the rate-limiting step of a reaction network and often display novel mechanisms and kinetics as compared to homogeneous chemistry.

  13. Storm Sewage Dilution in Smaller Streams

    DEFF Research Database (Denmark)

    Larsen, Torben; Vestergaard, Kristian

    1987-01-01

    A numerical model has been used to show how dilution in smaller streams can be effected by unsteady hydraulic conditions caused by a storm sewage overflow.......A numerical model has been used to show how dilution in smaller streams can be effected by unsteady hydraulic conditions caused by a storm sewage overflow....

  14. Gibbs free energy of transfer of a methylene group on {l_brace}UCON + (sodium or potassium) phosphate salts{r_brace} aqueous two-phase systems: Hydrophobicity effects

    Energy Technology Data Exchange (ETDEWEB)

    Silverio, Sara C. [LSRE - Laboratory of Separation and Reaction Engineering, Associate Laboratory LSRE/LCM, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias s/n. 4200-465 Porto (Portugal); IBB - Institute for Biotechnology and Bioengineering, Centre for Biological Engineering, University of Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Rodriguez, Oscar [LSRE - Laboratory of Separation and Reaction Engineering, Associate Laboratory LSRE/LCM, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias s/n. 4200-465 Porto. Portugal (Portugal); Teixeira, Jose A. [IBB - Institute for Biotechnology and Bioengineering, Centre for Biological Engineering, University of Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Macedo, Eugenia A., E-mail: eamacedo@fe.up.p [LSRE - Laboratory of Separation and Reaction Engineering, Associate Laboratory LSRE/LCM, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias s/n. 4200-465 Porto (Portugal)

    2010-08-15

    The Gibbs free energy of transfer of a suitable hydrophobic probe can be regarded as a measure of the relative hydrophobicity of the different phases. The methylene group (CH{sub 2}) can be considered hydrophobic, and thus be a suitable probe for hydrophobicity. In this work, the partition coefficients of a series of five dinitrophenylated-amino acids were experimentally determined, at 23 {sup o}C, in three different tie-lines of the biphasic systems: (UCON + K{sub 2}HPO{sub 4}), (UCON + potassium phosphate buffer, pH 7), (UCON + KH{sub 2}PO{sub 4}), (UCON + Na{sub 2}HPO{sub 4}), (UCON + sodium phosphate buffer, pH 7), and (UCON + NaH{sub 2}PO{sub 4}). The Gibbs free energy of transfer of CH{sub 2} units were calculated from the partition coefficients and used to compare the relative hydrophobicity of the equilibrium phases. The largest relative hydrophobicity was found for the ATPS formed by dihydrogen phosphate salts.

  15. PROPERTIES OF DILUTE SOLUTIONS OF HYDROPHOBICALLY MODIFIED POLY(4-VINYL PYRIDINE) (POLYSOAPS)

    Institute of Scientific and Technical Information of China (English)

    1998-01-01

    Hydrophobically modified poly(4-vinyl pyridines) by alkyl bromides are kinds of polysoap similar to the surfactant. Properties of dilute solutions were studied through the viscosity measurements in pure water and NaCl solutions. In aqueous solutions of polysoaps hydrophobic interaction can be attributed to aggregation of hydrophobic groups of the polysoap main chains. The hydrophobic groups of polysoap can aggregate to form hydrophobic microdomains (micelles) in aqueous solution. This is a compact conformation. The formation of such microdomains is a process of dynamic equilibrium.

  16. Partition behaviors of oxytetracycline hydrochloride (OTC) in small molecule alcohol/salt binary aqueous two-phase system%小分子醇/盐二元双水相体系中盐酸土霉素的分配行为

    Institute of Scientific and Technical Information of China (English)

    关卫省; 柴丽; 韩娟

    2012-01-01

    Based on the aqueous two-phase system,a new method of using ethanol and re-propanol with sodium dihydrogen phosphate binary aqueous two-phase system for extracting of oxytetracycline hydrochloride (OTC) was set up. The influence factors on partition behaviors of oxytetracyeline hydrochloride (OTC) were studied,including the system composition,type and amount of salts,the pH value,the extraction temperature, and standing time after centrifuge. The results showed that the binary aqueous two-phase system can be used to study the distribution of antibiotics. When the system was ethanol and n-pro-panol, NaH2 PO4 concentration of 48% , the pH value was 4~ 5, temperature was 25℃, and standing 12 h ,the partition coefficient of oxytetracycline hydrochloride ( OTC) was 21.95, and extraction rate was 86.09%.%在双水相体系研究的基础上,建立了乙醇与正丙醇和磷酸二氢钠形成的二元双水相体系萃取盐酸土霉素的新方法,考察了小分子醇的用量、盐种类和浓度、pH值、温度以及静置时间对盐酸土霉素分配行为的影响.结果表明,小分子醇/盐二元双水相体系可用于抗生素分配行为的研究,其中体系组成为乙醇和正丙醇,磷酸二氢钠浓度在48%,pH值在4~5,温度25℃,以及静置12 h左右,盐酸土霉素在该二元双水相体系中的分配系数达到21.95,萃取率达86.09%.

  17. Hydroxide depletion in dilute supernates stored in waste tanks

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D.T.

    1985-10-10

    Free hydroxide ion in dilute supernates are depleted by reaction with atmospheric carbon dioxide to form bicarbonate and carbonate species and by reaction with acidic compounds formed by the radiolytic decomposition of tetraphenylborate salts. A model of the kinetics and thermodynamics of absorption of carbon dioxide in the waste tanks has been developed. Forecasts of the rate of hydroxide depletion and the requirements for sodium hydroxide to maintain technical standards have been made for the washed sludge and washed precipitate storage tanks. Hydroxide depletion is predicted to have a minimal impact on sludge processing operations. However, in-tank precipitation and downstream DWPF operations are predicted to be significantly affected by hydroxide depletion in Tank 49H. The installation of a carbon dioxide scrubber on Tank 49H may be justified in view of the decrease in alkali content and variation in the melter feed.

  18. 季铵盐壳聚糖膜对水体中十二烷基苯磺酸钠吸附的研究%Adsorption of Sodium Dodecylbenzenesulfonate from Aqueous Solution by Quaternary Chitosan Salt Membranes

    Institute of Scientific and Technical Information of China (English)

    黄晓东; 徐国钦; 娄本勇

    2012-01-01

    The quaternary chitosan salt membrane (QCSM)was prepared as an adsorbent by using chitosan as raw material, and its adsorption behavior for sodium dodecylbenzenesulfonate (SDBS)was studied. Effect factors such as solution pH, adsorption time, concentration and temperature were investigated. Results showed that pH 4.0 and shaking time 120min were the optima] conditions for adsorption of SDBS. The adsorption process followed a pseudo-second order equation and the equilibrium isotherm may be described by Langmuir model rather than the Freundlich and Tempkin model. Thermodynamic studies indicated that adsorption process was spontaneous and endothermic with an increase in entropy.%以壳聚糖为原料,制备季铵盐壳聚糖膜(QCSM)吸附剂,研究吸附剂对十二烷基苯磺酸钠(SDBS)的吸附性能,考察了溶液pH值、吸附时间、浓度和温度的影响.结果表明,吸附适宜条件的为:pH 4.0,吸附时间120 min,吸附过程可以很好地用准二级动力学方程描述,吸附等温线用Langmuir方程的拟合效果优于Freundlich和Tempkin方程.在热力学研究表中,△G0<0,△H0>0,△S0>0,表明此吸附过程是自发、吸热和熵增加的过程.

  19. On the attenuation of x-rays and gamma-rays in dilute solutions

    DEFF Research Database (Denmark)

    Gerward, Leif

    1996-01-01

    The theory of X-ray and gamma-ray attenuation in solutions is developed. The rule of mixture for the calculation of mass and linear attenuation coefficients is elaborated in the general case as well as in the limit of extreme dilution. The validity of the latter approximation is illustrated...... by the attenuation of 17.443 keV X-rays in aqueous solutions of NaCl. Copyright (C) 1996 Elsevier Science Ltd...

  20. Semi-dilute galactomannan solutions: observations on viscosity scaling behavior of guar gum

    Science.gov (United States)

    Pollard, Michael A.; Fischer, Peter

    2014-11-01

    Based on experimental work involving evaluation of viscosity enhancement of aqueous solutions by high molecular weight guar gum, we have observed that the shear viscosity scaling exponent b for semi-dilute solutions, ηsp ˜ (c[η])b, is sensitive to molecular weight, being approximately 4.7 for native samples and decreasing progressively as Mw is lowered. The critical overlap parameter demarcating the dilute and semi-dilute regimes also depends on the molecular weight as {{≤ft(c[η ]\\right)}*} ˜ Mw-0.82 . Consequently, viscosity-concentration plots fail to achieve overlap using only specific viscosity and overlap concentration as reducing variables, a commonly accepted empiricism for random-coil polysaccharides. To bridge the gap, we propose to account for water solubility, its temperature dependence and the resulting chain flexibility as additional factors to fully describe the solution behavior of these highly-important raw materials.

  1. DC electrophoresis and viscosity of realistic salt-free concentrated suspensions: non-equilibrium dissociation-association processes.

    Science.gov (United States)

    Ruiz-Reina, Emilio; Carrique, Félix; Lechuga, Luis

    2014-03-01

    Most of the suspensions usually found in industrial applications are concentrated, aqueous and in contact with the atmospheric CO2. The case of suspensions with a high concentration of added salt is relatively well understood and has been considered in many studies. In this work we are concerned with the case of concentrated suspensions that have no ions different than: (1) those stemming from the charged colloidal particles (the added counterions, that counterbalance their surface charge); (2) the H(+) and OH(-) ions from water dissociation, and (3) the ions generated by the atmospheric CO2 contamination. We call this kind of systems "realistic salt-free suspensions". We show some theoretical results about the electrophoretic mobility of a colloidal particle and the electroviscous effect of realistic salt-free concentrated suspensions. The theoretical framework is based on a cell model that accounts for particle-particle interactions in concentrated suspensions, which has been successfully applied to many different phenomena in concentrated suspensions. On the other hand, the water dissociation and CO2 contamination can be described following two different levels of approximation: (a) by local equilibrium mass-action equations, because it is supposed that the reactions are so fast that chemical equilibrium is attained everywhere in the suspension, or (b) by non-equilibrium dissociation-association kinetic equations, because it is considered that some reactions are not rapid enough to ensure local chemical equilibrium. Both approaches give rise to different results in the range from dilute to semidilute suspensions, causing possible discrepancies when comparing standard theories and experiments concerning transport properties of realistic salt-free suspensions.

  2. Semi-Passive Oxidation-Based Approaches for Control of Large, Dilute Groundwater Plumes of Chlorinated Ethylenes

    Science.gov (United States)

    2014-04-01

    Based Approaches for Control of Large, Dilute Groundwater Plumes of Chlorinated Ethylenes 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6...Numerous studies have reported that chemical oxidation of chlorinated ethylenes in aqueous solution is rapid (e.g. Yan and Schwartz, 1998; Huang et al

  3. On-site production of a dialysis bath from dry salts. Results of solute concentration control by routine clinical chemistry

    OpenAIRE

    Beige, Joachim; Lutter, Steffen; Martus, Peter

    2012-01-01

    Background. Dialysis bath production, at least in Europe, is currently based on pre-produced aqueous solutions of dialysis salts (concentrate), which are re-handled by dialysis machines to deliver the final dialysate concentrations. Because of the logistics of aqueous solution creation, a large amount of transportation capacity is needed. Therefore, we changed this process to use pre-produced dry salt containers and to undertake in-clinic dissolution of salts and concentration production. Bec...

  4. Physicochemical effects in aging aqueous Laponite suspensions.

    Science.gov (United States)

    Shahin, A; Joshi, Yogesh M

    2012-11-06

    We study aging behavior of an aqueous suspension of Laponite as a function of concentration of Laponite, concentration of salt, time elapsed since preparation of suspension (idle time), and temperature by carrying extensive rheological and conductivity experiments. We observe that temporal evolution of elastic moduli, which describes structural build-up and aging, shifts to low times for experiments carried out for higher concentration of Laponite, higher concentration of salt, greater temperature, and longer idle time while preserving the curvature of evolution in the solid regime (elastic modulus greater than viscous modulus). Consequently appropriate shifting of evolution of elastic modulus in the solid regime leads to aging time-idle time-salt concentration-Laponite concentration-temperature superposition. The existence of such a superposition suggests the generic nature of microstructure buildup irrespective of mentioned variables in the explored range. The behavior of shift factors needed to obtain the superposition indicate that the energy barrier associated with structural buildup decreases with an increase in idle time and temperature and decreases linearly with an increase in concentration of Laponite and that of salt. The conductivity experiments show that ionic conductivity of the suspension increases with increasing Laponite concentration, salt concentration, temperature, and very importantly the idle time. We also analyze the interparticle interactions using DLVO theory that suggests an increase in idle time, temperature, and salt concentration increases the height of the repulsive energy barrier while it decreases the width of the same when particles approach each other in a parallel fashion. However when particles approach each other in a perpendicular fashion, owing to dissimilar charges on edge and face, the energy barrier for the attractive interaction is expected to decrease with an increase in idle time, temperature, and salt concentration

  5. Effect of Added Salts or Polyols on the Cloud Point and the Liquid-Crystalline Structures of Polyoxyethylene-Modified Silicone.

    Science.gov (United States)

    Iwanaga; Kunieda

    2000-07-15

    The effect of added salts (NaCl, Na(2)SO(4), and NaSCN) or polyols (glycerin (Gly), 1,3-butanediol (1,3-BD), ethylene glycol (EG), and polyethylene glycol (PEG400)) on the hexagonal liquid-crystalline structure of polyoxyethylene-modified silicone was investigated by means of small angle X-ray scattering (SAXS). The effective cross-sectional area of the lipophilic part of the aggregate, a(s), in the hexagonal phase decreases upon the addition of salts, on one hand, lowering the cloud point in the dilute aqueous siloxane surfactant solutions. On the other hand, if added salt raises the cloud point, the a(s) increases. Similar results were obtained in the case of the addition of polyols. Since the a(s) mainly depends on the EO chain length, the above results are direct evidence that the hydration or dehydration of the EO chain is affected by these additives. The static fluorescence probe method was applied to the Gly and 1,3-BD systems using 8-anilino-1-naphthalene-sulfonic acid, ANS, to know the change in hydration of the EO chains. In the Gly system, the hydration of the EO chain monotonically decreases whereas 1,3-BD first increases the hydration and then decreases it at high 1,3-BD content. These results are very consistent with the SAXS and cloud temperature results. Copyright 2000 Academic Press.

  6. Novel understanding of calcium silicate hydrate from dilute hydration

    KAUST Repository

    Zhang, Lina

    2017-05-13

    The perspective of calcium silicate hydrate (C-S-H) is still confronting various debates due to its intrinsic complicated structure and properties after decades of studies. In this study, hydration at dilute suspension of w/s equaling to 10 was conducted for tricalcium silicate (C3S) to interpret long-term hydration process and investigate the formation, structure and properties of C-S-H. Based on results from XRD, IR, SEM, NMR and so forth, loose and dense clusters of C-S-H with analogous C/S ratio were obtained along with the corresponding chemical formulae proposed as Ca5Si4O13∙6.2H2O. Crystalline structure inside C-S-H was observed by TEM, which was allocated at the foil-like proportion as well as the edge of wrinkles of the product. The long-term hydration process of C3S in dilute suspension could be sketchily described as migration of calcium hydroxide and in-situ growth of C-S-H with equilibrium silicon in aqueous solution relatively constant and calcium varied.

  7. Uranium determination in sea water using the isotopic dilution technique and HR-ICPMS; Determinacao de uranio em agua do mar por meio da tecnica de diluicao isotopica e HR-ICPMS

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, Marcio Henrique da Costa; Sarkis, Jorge Eduardo de Souza; Hortellani, Marcos Antonio, E-mail: mhcper@yahoo.com.b, E-mail: jesarkis@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Nascimento, Marcos R.L. [Laboratorio de Pocos de Caldas (LAPOC/CNEN-MG), MG (Brazil)

    2009-07-01

    In this work, the uranium total and the isotopic composition in seawater were calculated using the isotopic dilution applied to the mass spectrometry. The used tracer was a {sup 233}U solution . Near 99 % of the present salts in the matrix were separated by evaporation up to the saturation point. The uranium present in aqueous phase was separated from the matrix through the ion exchange chromatography using the strong Dowex 1 x 8 200-400 mesh anionic resin in chloridric medium 12 M. The analyses were performed in a high resolution mass spectrometer with plasma inductively coupled source. The method validation was done using the seawater standard CASS-4 (Near shore Seawater Reference Material for Trace metals) produced by the NRC C. The procedure allowed to obtain the fractions exempt of salts, having as consequence a greater stability in the analytical signal, and a rise in the instrumental revenue for a great number of samples. The uranium found in the samples was present in levels considered naturals and were obtained with a precision near 2 %

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

    OpenAIRE

    Kempe, Henrik; Kempe, Maria

    2010-01-01

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

  9. The antibacterial activity of diluted Tualang honey

    Directory of Open Access Journals (Sweden)

    N. A. Roslan

    2015-05-01

    Full Text Available Tualang honey (TH is a Malaysian jungle honey obtained from the wild. The honey is produced by the rock bee (Apis dorsata, which builds hives on branches of tall Tualang (Koompassia excelsa (Becc. Taub trees located mainly in the north-western region of Peninsular Malaysia. Limited information is available on the antibacterial mechanism of local honey. The present study was conducted to determine the antibacterial activity of diluted ?Tualang? honey against Escherichia coli (E. coli. Three different Tualang honey concentrations, namely, 20, 30 and 40% were used to examine the effect of diluting Tualang honey on its antibacterial effect towards E. coli. The 40% diluted honey was the most effective in inhibiting the growth of E. coli, followed by honey diluted at 20 and 30%. The high antibacterial activity of honey towards E. Coli was thought to arise from the production of hydrogen peroxide, but requires further study to validate the action.

  10. Flux balance analysis accounting for metabolite dilution.

    Science.gov (United States)

    Benyamini, Tomer; Folger, Ori; Ruppin, Eytan; Shlomi, Tomer

    2010-01-01

    Flux balance analysis is a common method for predicting steady-state flux distributions within metabolic networks, accounting for the growth demand for the synthesis of a predefined set of essential biomass precursors. Ignoring the growth demand for the synthesis of intermediate metabolites required for balancing their dilution leads flux balance analysis to false predictions in some cases. Here, we present metabolite dilution flux balance analysis, which addresses this problem, resulting in improved metabolic phenotype predictions.

  11. Surface tension and related thermodynamic quantities of aqueous electrolyte solutions

    CERN Document Server

    Matubayasi, Norihiro

    2013-01-01

    Surface tension provides a thermodynamic avenue for analyzing systems in equilibrium and formulating phenomenological explanations for the behavior of constituent molecules in the surface region. While there are extensive experimental observations and established ideas regarding desorption of ions from the surfaces of aqueous salt solutions, a more successful discussion of the theory has recently emerged, which allows the quantitative calculation of the distribution of ions in the surface region. Surface Tension and Related Thermodynamic Quantities of Aqueous Electrolyte Solutions provides a d

  12. Understanding the crystallisation of an acidic protein by dilution in the ternary NaCl-2-methyl-2,4-pentanediol-H 2O system

    Science.gov (United States)

    Costenaro, Lionel; Zaccai, Giuseppe; Ebel, Christine

    2001-11-01

    Halophilic malate dehydrogenase is a negatively charged protein that crystallises well in a dilution process following a complex interplay with the three components of NaCl-MPD-H 2O solvents (MPD: 2-methyl-2,4-pentanediol). The process was characterised by measuring the folding state of the protein, its concentration, its apparent solubility and second virial coefficients in various NaCl-MPD-H 2O ratios representative of the phase diagram of the system. The protein crystallises by vapour diffusion between a drop containing protein in aqueous NaCl and MPD and a bath containing a given percentage of MPD in water. The starting drop is bi-phasic, in which the protein is concentrated in the salt-rich phase. This phase evolves towards a solution less concentrated in both NaCl and protein but more concentrated in MPD, before the system is driven to a single-phase region, where crystals are obtained. The protein stability is preserved during its crystallisation. We showed from second virial coefficient measurements that crystal formation is correlated with a slow evolution from repulsive to attractive protein-protein interactions. The end of the vapour diffusion process between the drop and the bath corresponds to a decrease of the attractive interaction, which we suggest favours crystal growth. The application of these results to crystallisation of other charged proteins and nucleic acids is discussed.

  13. The behaviour of salt and salt caverns

    NARCIS (Netherlands)

    Fokker, P.A.

    1995-01-01

    Salts are mined for both storage and extraction purposes, either via dry or solution mining techniques. For operational, environmental and geological purposes, it is important to understand and predict the in situ behaviour of salt, in particular the creep and strength characteristics. A micro-mecha

  14. Precipitation of neptunium dioxide from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Roberts, K E

    1999-12-01

    Tens of thousands of metric tons of highly radioactive, nuclear waste have been generated in the US. Currently, there is no treatment or disposal facility for these wastes. Of the radioactive elements in high-level nuclear waste, neptunium (Np) is of particular concern because it has a long half-life and may potentially be very mobile in groundwaters associated with a proposed underground disposal site at Yucca Mountain, Nevada. Aqueous Np concentrations observed in previous, short-term solubility experiments led to calculated potential doses exceeding proposed long-term regulatory limits. However, thermodynamic data for Np at 25 C showed that these observed aqueous Np concentrations were supersaturated with respect to crystalline NpO{sub 2}. It was hypothesized that NpO{sub 2} is the thermodynamically stable solid phase in aqueous solution, but it is slow to form in an aqueous solution of NpO{sub 2}{sup +} on the time scale of previous experiments. The precipitation of NpO{sub 2} would provide significantly lower aqueous Np concentrations leading to calculated doses below proposed regulatory limits. To test this hypothesis, solubility experiments were performed at elevated temperature to accelerate any slow precipitation kinetics. Ionic NpO{sub 2}{sup +} (aq) was introduced into very dilute aqueous solutions of NaCl with initial pH values ranging from 6 to 10. The reaction vessels were placed in an oven and allowed to react at 200 C until steady-state aqueous Np concentrations were observed. In all cases, aqueous Np concentrations decreased significantly from the initial value of 10{sup {minus}4} M. The solids that formed were analyzed by x-ray powder diffraction, x-ray absorption spectroscopy, and scanning electron microscopy. The solids were determined to be high-purity crystals of NpO{sub 2}. This is the first time that crystalline NpO{sub 2} has been observed to precipitate from NpO{sub 2}{sup +}(aq) in near-neutral aqueous solutions. The results obtained

  15. Cooking without salt

    Science.gov (United States)

    DASH diet; High blood pressure - DASH; Hypertension - DASH; Low-salt diet - DASH ... Explore cooking with salt substitutes. Add a splash of lemon and other citrus fruits, or wine, to soups and other dishes. Or use them ...

  16. Salt-free vesicle-phases and their template effect

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Researches on the construction, structure, and formation of vesicles formed from surfactants have attracted great attention from colloid and interface chemists. The vesicles formed from salt-free cationic-anionic surfactant systems are very different from those with excess salts, having many particular properties. In this paper, we introduce the properties of vesicles prepared from salt-free surfactant systems, according to our own results, especially the vesicles formed from surfactants with divalent metal ions as counterions in aqueous solutions and room temperature ionic liquids. Moreover, the primary results on template effect of the metal-ligand vesicles have also been summarized.

  17. Molecular Thermodynamic Model for Polyelectrolyte Solutions with Added Salts

    Institute of Scientific and Technical Information of China (English)

    ZHANGBo; CAIJun; 等

    2002-01-01

    A molecular thermodynamic model of polyelectrolyte developed previously was extended to polyelectrolyte solutions with added salts.Thermodynamic properties,such as activity coefficients of polyelectrolytes or added salts and osmotic coefficients of solvent, of a number of aqueous mixtures of polyelectrolytes and salts are analyzed with the proposed model.Successful correlation is obtained in the range of moderate or higher polyion concentration.For the same sample,thermodynamic properties of polyelectrolytes with and without simple electrolytes can be predicted mutually using parameters from regression data.

  18. Reduced osmolarity oral rehydration salt in Cholera.

    Science.gov (United States)

    Faruque, A S; Mahalanabis, D; Hamadani, J D; Zetterstrom, R

    1996-01-01

    In a controlled clinical trial conducted in 34 adults with severe cholera diarrhoea, the use of a relatively dilute oral rehydration salt (ORS) solution (sodium 67, potassium 20, chloride 66, citrate 7, glucose 89 mmol/l, osmolality 249 mOsmol/kg) caused a 29% (p=0.003) reduction in stool output over the first 24 h and a 37% (p=0.001) reduction over the first 48 h compared with 29 controls who received the hyperosmolar WHO/UNICEF ORS. No controls but 3 study-group patients had marked but asymptomatic hyponatraemia (sodium cholera.

  19. Solid-liquid (S-L) an liquid (L-L) phase transfer of salts via ‘encapsulated’ crown ether cation complexes

    NARCIS (Netherlands)

    Reinhoudt, D.N.

    1983-01-01

    In recent years crown ethers have been successfully used for the transport of salts, both inorganic and organic, from an aqueous phase to organic solvents. Our work has extended the applicability of these crown ethers to the transport of salts from the solid state into solution both aqueous and nona

  20. Critical properties of aqueous solutions. Part 1: Experimental data

    Science.gov (United States)

    Abdulagatov, A. I.; Stepanov, G. V.; Abdulagatov, I. M.

    2008-08-01

    All data available in the literature on the critical properties of binary aqueous solutions like H2O + common salt, H2O + hydrocarbon, H2O + alcohol, H2O + gas, and others are gathered. Methods for determining them are presented together with errors and concentration measurement intervals for each source of data. The format in which the data are presented will allow the readers to quickly find the necessary information on the critical properties of aqueous solutions from the original sources and use them for solving scientific and engineering tasks. Certain general features of the critical lines and phase diagrams of aqueous solutions with volatile and nonvolatile components are discussed.

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

    DEFF Research Database (Denmark)

    Pennathur, Sumita; Kristensen, Jesper; Crumrine, Andrew

    2011-01-01

    conductance for low salt concentrations, we identify a minimum conductance value before saturation at a value independent of salt concentration in the dilute limit. Our model self-consistently couples chemical equilibrium models of the silica wall and the electrolyte bulk, and is parameterized by only...

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

    DEFF Research Database (Denmark)

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

    2011-01-01

    the nanochannel conductance at low salt concentrations and identify a conductance minimum before saturation at a value independent of salt concentration in the dilute limit. Via the Poisson-Boltzmann equation, our model self-consistently couples chemical-equilibrium dissociation models of the silica wall...

  3. 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

    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...

  4. The salts of Mars

    Science.gov (United States)

    Clark, B. C.; Van Hart, D. C.

    1981-01-01

    Salt compounds are apparently an important component of the fine-grained regolith on Mars. Salt enrichment may be explained either as a secondary concentration of chemical weathering products or as direct incorporation of planetary released volatiles. Geochemical measurements and chemical relationships constrain the salt species and resultant physicochemical consequences. A likely assemblage is dominated by (Mg,Na)SO4, NaCl, and (Mg,Ca)CO3. Formation of brine in equilibrium with such a salt mixture is unlikely under the temperature and water-vapor restrictions prevalent over most, if not all, of the Martian surface. Acidic conditions, accompanying salt formation, favor the preferential destruction of susceptible igneous minerals.

  5. Salting Effects as an Illustration of the Relative Strength of Intermolecular Forces

    Science.gov (United States)

    Person, Eric C.; Golden, Donnie R.; Royce, Brenda R.

    2010-01-01

    This quick and inexpensive demonstration of the salting of an alcohol out of an aqueous solution illustrates the impact of intermolecular forces on solubility using materials familiar to many students. Ammonium sulfate (fertilizer) is added to an aqueous 35% solution of isopropyl alcohol (rubbing alcohol and water) containing food coloring as a…

  6. Amino Acid Salts for Carbon Dioxide Capture: Evaluating l-Prolinate at Desorber Conditions

    NARCIS (Netherlands)

    Majchrowicz, Magdalena Elzbieta; Brilman, Wim

    2015-01-01

    Vapor–liquid equilibrium (VLE) measurements for unloaded and CO2-saturated aqueous potassium salt solutions of l-proline have been performed using a high-pressure equilibrium cell. The solubility of CO2 has been determined at temperatures of 363, 393, and 403 K in 3 and 4 mol dm–3 aqueous solutions.

  7. Recent results on aqueous electrolyte cells

    KAUST Repository

    Wessells, Colin

    2011-03-01

    The improved safety of aqueous electrolytes makes aqueous lithium-ion batteries an attractive alternative to commercial cells utilizing flammable and expensive organic electrolytes. Two important issues relating to their use have been addressed in this work. One is the extension of the usable voltage range by the incorporation of lithium salts, and the other is the investigation of a useful negative electrode reactant, LiTi 2(PO 4) 3. The electrochemical stability of aqueous lithium salt solutions containing two lithium salts, LiNO 3 and Li 2SO 4, has been characterized using a constant current technique. In both cases, concentrated solutions had effective electrolyte stability windows substantially greater than that of pure water under standard conditions. At an electrolyte leakage current of 10 μA cm -2 between two platinum electrodes in 5 M LiNO 3 the cell voltage can reach 2.0 V, whereas with a leakage current of 50 μA cm -2 it can reach 2.3 V. LiTi 2(PO 4) 3 was synthesized using a Pechini method and cycled in pH-neutral Li 2SO 4. At a reaction potential near the lower limit of electrolyte stability, an initial discharge capacity of 118 mAh g -1 was measured at a C/5 rate, while about 90% of this discharge capacity was retained after 100 cycles. This work demonstrates that it is possible to have useful aqueous electrolyte lithium-ion batteries using the LiTi 2(PO 4) 3 anode with cell voltages of 2 V and above. © 2010 Elsevier B.V. All rights reserved.

  8. 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.

  9. Order Parameters of the Dilute A Models

    CERN Document Server

    Warnaar, S O; Seaton, K A; Nienhuis, B

    1993-01-01

    The free energy and local height probabilities of the dilute A models with broken $\\Integer_2$ symmetry are calculated analytically using inversion and corner transfer matrix methods. These models possess four critical branches. The first two branches provide new realisations of the unitary minimal series and the other two branches give a direct product of this series with an Ising model. We identify the integrable perturbations which move the dilute A models away from the critical limit. Generalised order parameters are defined and their critical exponents extracted. The associated conformal weights are found to occur on the diagonal of the relevant Kac table. In an appropriate regime the dilute A$_3$ model lies in the universality class of the Ising model in a magnetic field. In this case we obtain the magnetic exponent $\\delta=15$ directly, without the use of scaling relations.

  10. 21 CFR 864.5240 - Automated blood cell diluting apparatus.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Automated blood cell diluting apparatus. 864.5240... § 864.5240 Automated blood cell diluting apparatus. (a) Identification. An automated blood cell diluting apparatus is a fully automated or semi-automated device used to make appropriate dilutions of a blood...

  11. Dynamic Dilution Effects in Polymeric Networks

    DEFF Research Database (Denmark)

    Skov, Anne Ladegaard; Sommer-Larsen, Peter; Hassager, Ole

    2006-01-01

    processes, namely the reptation of linear species within the network and the arm withdrawal process of star arms in the sol fraction and of dangling single-chain ends attached to the network. The relaxation spectra are influenced by the stoichiometry to a large extent due to dynamic dilution effects caused...... by the change in the amount of dangling arms and solubles with stoichiometry. The star arm relaxation is suppressed by washing out the sol fraction which is seen as a clear example of the dynamic dilution effect arising from the small amount of non-reactive PDMS....

  12. Thermodynamic studies of ionic hydration and interactions for amino acid ionic liquids in aqueous solutions at 298.15 K.

    Science.gov (United States)

    Dagade, Dilip H; Madkar, Kavita R; Shinde, Sandeep P; Barge, Seema S

    2013-01-31

    's free energy data and literature enthalpy data. This study highlights that the hydrophobic interaction persists even in the limit of infinite dilution where the hydration effects are usually dominant, implying importance of hydrophobic hydration. Analysis of the results further shows that the hydration of amino acid ionic liquids occurs through the cooperative H-bond formation with the kosmotropic effect in contrast to the usual inorganic salts or hydrophobic salts like tetraalkylammonium halides.

  13. Geochemical detection of carbon dioxide in dilute aquifers

    Directory of Open Access Journals (Sweden)

    Aines Roger

    2009-03-01

    Full Text Available Abstract Background Carbon storage in deep saline reservoirs has the potential to lower the amount of CO2 emitted to the atmosphere and to mitigate global warming. Leakage back to the atmosphere through abandoned wells and along faults would reduce the efficiency of carbon storage, possibly leading to health and ecological hazards at the ground surface, and possibly impacting water quality of near-surface dilute aquifers. We use static equilibrium and reactive transport simulations to test the hypothesis that perturbations in water chemistry associated with a CO2 gas leak into dilute groundwater are important measures for the potential release of CO2 to the atmosphere. Simulation parameters are constrained by groundwater chemistry, flow, and lithology from the High Plains aquifer. The High Plains aquifer is used to represent a typical sedimentary aquifer overlying a deep CO2 storage reservoir. Specifically, we address the relationships between CO2 flux, groundwater flow, detection time and distance. The CO2 flux ranges from 103 to 2 × 106 t/yr (0.63 to 1250 t/m2/yr to assess chemical perturbations resulting from relatively small leaks that may compromise long-term storage, water quality, and surface ecology, and larger leaks characteristic of short-term well failure. Results For the scenarios we studied, our simulations show pH and carbonate chemistry are good indicators for leakage of stored CO2 into an overlying aquifer because elevated CO2 yields a more acid pH than the ambient groundwater. CO2 leakage into a dilute groundwater creates a slightly acid plume that can be detected at some distance from the leak source due to groundwater flow and CO2 buoyancy. pH breakthrough curves demonstrate that CO2 leaks can be easily detected for CO2 flux ≥ 104 t/yr within a 15-month time period at a monitoring well screened within a permeable layer 500 m downstream from the vertical gas trace. At lower flux rates, the CO2 dissolves in the aqueous phase

  14. Effect of halophilic LAB and yeasts on the quality of high-salt dilute-state soy sauce%耐盐乳酸菌和酵母菌对高盐稀态发酵酱油品质的影响

    Institute of Scientific and Technical Information of China (English)

    崔瑞迎; 郑佳; 梁如; 何翠容; 陈勇; 黄钧; 吴重德; 周荣清

    2013-01-01

    研究了添加耐盐乳酸菌(Tetragenococcus halophilus)和酵母菌(Zygosaccharomyces rouxii和Candida versatilis)对酱醪理化指标及挥发性组分的影响.研究结果表明,添加耐盐微生物的酱醪发酵125d后氨态氮(FN)均略高于对照样品(未添加耐盐微生物);添加T.halophilus的酱醪总酸(TA)高于其他样品,而采用T.halophilus、Z.rouxii和C.versatilis 共培养的酱醪TA和对照样品没有显著区别;分析酱醪还原糖(RS)含量结果表明,添加耐盐微生物后还原糖含量显著低于对照样品.此外,通过GC-MS分析了添加耐盐乳酸菌和酵母菌对酱醪挥发性组分的影响.发酵125d后,醇、酯类组分含量增加,酸类及其他类组分含量减少.所检出的各酱醪挥发性组分中,添加T.halophilus的酱醪中2-甲基丁酸、2-甲基丁醇、乙酸异戊酯含量分别较对照组高53.4%、337.3%、388.2%,添加Z.rouxii和C.versatilis的酱醪中乙醇和乙酸乙酯含量分别较对照组高64.2%和56.3%,采用T.halophilus、Z.rouxii和C.versatilis共培养的酱醪中1-辛烯-3-醇和苯甲醛含量高于对照样品56.7%和26.3%,显著改善了酱醪风味.%Effects of halophilic LAB (Tetragenococcus halophilus) and yeasts (Zygosaccharomyces rouxii and Candida versatilis) on physicochemical properties and volatile compounds of soy sauce mash were investigated. The result showed that the FN of soy sauce mash added with salt-tolerance microorganisms at 125d were higher than that of the control sample (without microorganism addition), and the TA of soy sauce mash added with T. halophilus was higher than others. No obvious difference was observed in control sample and soy sauce mash added with T. halophilus, Z. rouxii and C. versatilis. Meanwhile, analysis of the changes of RS showed that the halotolerant microorganisms added samples exhibited lower content of RS compared to the control. Moreover, effects of volatile compounds in all soy sauce mash were analyzed

  15. Salt splitting using ceramic membranes

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-10-01

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

  16. APPLICATION OF NONIONIC TEMPERATURE SENSITIVE HYDROGEL FOR CONCENTRATION OF PROTEIN AQUEOUS SOLUTION

    Institute of Scientific and Technical Information of China (English)

    SUN Yishi; QIU Zhiyong; HONG Yaoliang

    1992-01-01

    Six different N-alkyl substituted acrylamide nonionic hydrogels were prepared and their swelling characteristics were measured. Poly N-isopropyl acrylamide (PNIPA) and poly N-n-propylacrylamide (PNNPA) temperature sensitive hydrogels were chosen as the nonionic temperature sensitive hydrogels for concentration of very dilute aqueous protein solution. The separation properties of PNIPA and PNNPA hydrogels with different network dimensions were studied and the modification of the hydrogels was surveyed in order to decrease their surface adsorption of protein molecules. The experimental results of the concentration of BSA (Bovin serum albumin) dilute aqueous solution by hydroxylpropyl methacrylate (HPMA) copolymerized PNIPA hydrogel were given. The value and the limitation of concentration of dilute aqueous protein solution by this method was evaluated.

  17. Confluence Model or Resource Dilution Hypothesis?

    DEFF Research Database (Denmark)

    Jæger, Mads

    Studies on family background often explain the negative effect of sibship size on educational attainment by one of two theories: the Confluence Model (CM) or the Resource Dilution Hypothesis (RDH). However, as both theories – for substantively different reasons – predict that sibship size should...

  18. Variational approach to the dilute Bose gas

    NARCIS (Netherlands)

    Bijlsma, M.; Stoof, H.T.C.

    1997-01-01

    We study the weakly interacting Bose gas in both two and three dimensions using a variational approach. In particular we construct the thermodynamic potential of the gas to within ladder approximation and find by minimization an accurate mean-field description of the dilute Bose gas. Using

  19. A century of indicator dilution technique

    DEFF Research Database (Denmark)

    Henriksen, Jens H; Jensen, Gorm B; Larsson, Henrik B W

    2014-01-01

    This review imparts the history and the present status of the indicator dilution technique with quantitative bolus injection. The first report on flow measurement with this technique appeared 100 years ago. In 1928, the use of intravascular dyes made possible a widespread application in animals...

  20. Serial dilution microchip for cytotoxicity test

    Science.gov (United States)

    Bang, Hyunwoo; Lim, Sun Hee; Lee, Young Kyung; Chung, Seok; Chung, Chanil; Han, Dong-Chul; Chang, Jun Keun

    2004-08-01

    Today's pharmaceutical industry is facing challenges resulting from the vast increases in sample numbers produced by high-throughput screening (HTS). In addition, the bottlenecks created by increased demand for cytotoxicity testing (required to assess compound safety) are becoming a serious problem. We have developed a polymer PDMS (polydimethylsiloxane) based microfluidic device that can perform a cytotoxicity test in a rapid and reproducible manner. The concept that the device includes is well adjustable to automated robots in huge HTS systems, so we can think of it as a potential dilution and delivery module. Cytotoxicity testing is all about the dilution and dispensing of a drug sample. Previously, we made a PDMS based microfluidic device which automatically and precisely diluted drugs with a buffer solution with serially increasing concentrations. This time, the serially diluted drug solution was directly delivered to 96 well plates for cytotoxicity testing. Cytotoxic paclitaxel solution with 2% RPMI 1640 has been used while carrying out cancerous cell based cytotoxicity tests. We believe that this rapid and robust use of the PDMS microchip will overcome the growing problem in cytotoxicity testing for HTS.

  1. Osmosis is not driven by water dilution.

    Science.gov (United States)

    Kramer, Eric M; Myers, David R

    2013-04-01

    There is a misconception among plant scientists that osmosis is driven by the tendency of solutes to dilute water. In this opinion article, we discuss the quantitative and qualitative failures of this view, and go on to review the correct kinetic picture of osmosis as it appears in physics textbooks.

  2. Organic non-aqueous cation-based redox flow batteries

    Energy Technology Data Exchange (ETDEWEB)

    Jansen, Andrew N.; Vaughey, John T.; Chen, Zonghai; Zhang, Lu; Brushett, Fikile R.

    2016-03-29

    The present invention provides a non-aqueous redox flow battery comprising a negative electrode immersed in a non-aqueous liquid negative electrolyte, a positive electrode immersed in a non-aqueous liquid positive electrolyte, and a cation-permeable separator (e.g., a porous membrane, film, sheet, or panel) between the negative electrolyte from the positive electrolyte. During charging and discharging, the electrolytes are circulated over their respective electrodes. The electrolytes each comprise an electrolyte salt (e.g., a lithium or sodium salt), a transition-metal free redox reactant, and optionally an electrochemically stable organic solvent. Each redox reactant is selected from an organic compound comprising a conjugated unsaturated moiety, a boron cluster compound, and a combination thereof. The organic redox reactant of the positive electrolyte is selected to have a higher redox potential than the redox reactant of the negative electrolyte.

  3. Submarine Salt Karst Terrains

    Directory of Open Access Journals (Sweden)

    Nico Augustin

    2016-06-01

    Full Text Available Karst terrains that develop in bodies of rock salt (taken as mainly of halite, NaCl are special not only for developing in one of the most soluble of all rocks, but also for developing in one of the weakest rocks. Salt is so weak that many surface-piercing salt diapirs extrude slow fountains of salt that that gravity spread downslope over deserts on land and over sea floors. Salt fountains in the deserts of Iran are usually so dry that they flow at only a few cm/yr but the few rain storms a decade so soak and weaken them that they surge at dm/day for a few days. We illustrate the only case where the rates at which different parts of one of the many tens of subaerial salt karst terrains in Iran flows downslope constrains the rates at which its subaerial salt karst terrains form. Normal seawater is only 10% saturated in NaCl. It should therefore be sufficiently aggressive to erode karst terrains into exposures of salt on the thousands of known submarine salt extrusions that have flowed or are still flowing over the floors of hundreds of submarine basins worldwide. However, we know of no attempt to constrain the processes that form submarine salt karst terrains on any of these of submarine salt extrusions. As on land, many potential submarine karst terrains are cloaked by clastic and pelagic sediments that are often hundreds of m thick. Nevertheless, detailed geophysical and bathymetric surveys have already mapped likely submarine salt karst terrains in at least the Gulf of Mexico, and the Red Sea. New images of these two areas are offered as clear evidence of submarine salt dissolution due to sinking or rising aggressive fluids. We suggest that repeated 3D surveys of distinctive features (± fixed seismic reflectors of such terrains could measure any downslope salt flow and thus offer an exceptional opportunity to constrain the rates at which submarine salt karst terrains develop. Such rates are of interest to all salt tectonicians and the many

  4. Kinetics and mechanism of acid-catalyzed hydrolysis of the diazo functional groups of 1-diazo-2-indanone and 2-diazo-1-indanone in aqueous solution

    National Research Council Canada - National Science Library

    Chiang, Yvonne; Kresge, A J; Sadovski, Oleg; Zeng, Xiaofeng; Zhu, Yu

    2005-01-01

    Rates of hydrolysis of 1-diazo-2-indanone and 2-diazo-1-indanone were measured in dilute aqueous perchloric acid solutions using both H2O and D2O as the solvent, and rates of hydrolysis of the latter...

  5. Treatment of plutonium process residues by molten salt oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Stimmel, J.; Wishau, R.; Ramsey, K.B.; Montoya, A.; Brock, J. [Los Alamos National Lab., NM (United States); Heslop, M. [Naval Surface Warfare Center (United States). Indian Head Div.; Wernly, K. [Molten Salt Oxidation Corp. (United States)

    1999-04-01

    Molten Salt Oxidation (MSO) is a thermal process that can remove more than 99.999% of the organic matrix from combustible {sup 238}Pu material. Plutonium processing residues are injected into a molten salt bed with an excess of air. The salt (sodium carbonate) functions as a catalyst for the conversion of the organic material to carbon dioxide and water. Reactive species such as fluorine, chlorine, bromine, iodine, sulfur, phosphorous and arsenic in the organic waste react with the molten salt to form the corresponding neutralized salts, NaF, NaCl, NaBr, NaI, Na{sub 2}SO{sub 4}, Na{sub 3}PO{sub 4} and NaAsO{sub 2} or Na{sub 3}AsO4. Plutonium and other metals react with the molten salt and air to form metal salts or oxides. Saturated salt will be recycled and aqueous chemical separation will be used to recover the {sup 238}Pu. The Los Alamos National Laboratory system, which is currently in the conceptual design stage, will be scaled down from current systems for use inside a glovebox.

  6. EXAFS studies of actinide ions in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Karim, D P; Georgopoulos, P; Knapp, G S

    1979-01-01

    The applicability of the EXAFS technique in the study of actinide systems is discussed. Uranium L/sub III/-edge spectra obtained on an in-lab rotating anode EXAFS facility are presented and analyzed for crystalline UO/sub 2/F/sub 2/ and aqueous solutions containing hexavalent uranium ions. Methods for the extension of the technique to more dilute systems are discussed.

  7. Structure of concentrated aqueous solutions of scandium chloride

    Science.gov (United States)

    Smirnov, P. R.; Grechin, O. V.

    2017-03-01

    It is shown via X-ray diffraction that aqueous solutions of scandium chloride form ionic associates in a wide range of concentrations. It is established that the Sc3+ ion coordination number increases upon dilution to 8.2 at an unchanged Sc3+-OH2 distance of 0.215 nm. The second coordination sphere of the cation forms at an average distance of 0.420 nm. The number of solvent molecules in the sphere logically increases during dilution. It is concluded that the anion does not form its own sphere in highly concentrated solutions. This coordination sphere begins to form only in solutions with moderate concentrations at a distance of 0.315 nm, and it contains six water molecules in diluted solutions.

  8. Rheology of semi-dilute solutions of calf-thymus DNA

    Indian Academy of Sciences (India)

    Ranjini Bandyopadhyay; A K Sood

    2002-04-01

    We study the rheology of semi-dilute solutions of the sodium salt of calf-thymus DNA in the linear and nonlinear regimes. The frequency response data can be fitted very well to the hybrid model with two dominant relaxation times 0 and 1. The ratio (0/1)∼ 5 is seen to be fairly constant on changing the temperature from 20 to 30°C. The shear rate dependence of viscosity can be fitted to the Carreau model.

  9. Using chitosan as a thickener for electrospinning dilute PVA solutions to improve fibre uniformity

    Science.gov (United States)

    Lin, Tong; Fang, Jian; Wang, Hongxia; Cheng, Tong; Wang, Xungai

    2006-08-01

    Chitosan was added to PVA aqueous solutions as a thickener to improve the electrospinning process. The presence of a small amount of chitosan considerably improved the uniformity of as-spun nanofibres. This improvement is attributed to its significant effect on the solution viscosity and conductivity, with only a slight impact on the surface tension. The concentration of the PVA required to produce bead-free and uniform nanofibres was reduced with the increase in chitosan concentration. The chitosan thickener suppressed the jet break-up and facilitated the jet stretching so that fine and uniform fibres could be electrospun even from a dilute PVA solution.

  10. Using chitosan as a thickener for electrospinning dilute PVA solutions to improve fibre uniformity

    Energy Technology Data Exchange (ETDEWEB)

    Lin Tong; Fang Jian; Wang Hongxia; Cheng Tong; Wang Xungai [Centre for Material and Fibre Innovation, Faculty of Science and Technology, Deakin University, Geelong, VIC 3217 (Australia)

    2006-08-14

    Chitosan was added to PVA aqueous solutions as a thickener to improve the electrospinning process. The presence of a small amount of chitosan considerably improved the uniformity of as-spun nanofibres. This improvement is attributed to its significant effect on the solution viscosity and conductivity, with only a slight impact on the surface tension. The concentration of the PVA required to produce bead-free and uniform nanofibres was reduced with the increase in chitosan concentration. The chitosan thickener suppressed the jet break-up and facilitated the jet stretching so that fine and uniform fibres could be electrospun even from a dilute PVA solution.

  11. Extraction Behaviour of Hexavalent Plutonium in the System of Dilute TBP/Kerosene

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    On the basis of the preparation and stabilization of Pu(Ⅵ), the distribution of it between dilute TBP/kerosene and aqueous phase is studied. The influences of the concentration of TBP, HNO3, A1(NO3)3, TBP and UO2(NO3)2 on the extraction of Pu(Ⅵ) by 5%TBP/kerosene are investigated at 28 ℃. The extraction reaction equation, the corresponding apparent equilibrium constant and the free energy change of it at temperature of 28 ℃ are obtained as follows:

  12. Luminescence properties of dilute bismide systems

    Energy Technology Data Exchange (ETDEWEB)

    Breddermann, B., E-mail: benjamin.breddermann@physik.uni-marburg.de [Faculty of Physics, Philipps-Universität Marburg, 35032 Marburg (Germany); Bäumner, A.; Koch, S.W.; Ludewig, P.; Stolz, W.; Volz, K. [Faculty of Physics, Philipps-Universität Marburg, 35032 Marburg (Germany); Hader, J.; Moloney, J.V. [Nonlinear Control Strategies Inc, 3542 N. Geronimo Ave., Tucson, AZ 85705 (United States); Broderick, C.A.; O' Reilly, E.P. [Tyndall National Institute, Lee Maltings, Dyke Parade, Cork (Ireland); Department of Physics, University College Cork, Cork (Ireland)

    2014-10-15

    Systematic photoluminescence measurements on a series of GaBi{sub x}As{sub 1−x} samples are analyzed theoretically using a fully microscopic approach. Based on sp{sup 3}s{sup ⁎} tight-binding calculations, an effective k·p model is set up and used to compute the band structure and dipole matrix elements for the experimentally investigated samples. With this input, the photoluminescence spectra are calculated using a systematic microscopic approach based on the semiconductor luminescence equations. The detailed theory-experiment comparison allows us to quantitatively characterize the experimental structures and to extract important sample parameters. - Highlights: • Measurement of photoluminescence spectra of a home grown series of dilute bismides. • Fully microscopic calculation of luminescence spectra from detailed band structure. • Quantitative experiment-theory comparison of luminescence spectra. • Thorough understanding of optoelectronic properties of dilute bismide material system. • Promising perspectives for the development of new device applications.

  13. Bond diluted anisotropic quantum Heisenberg model

    Energy Technology Data Exchange (ETDEWEB)

    Akıncı, Ümit, E-mail: umit.akinci@deu.edu.tr

    2013-10-15

    Effects of the bond dilution on the critical temperatures, phase diagrams and the magnetization behaviors of the isotropic and anisotropic quantum Heisenberg model have been investigated in detail. For the isotropic case, bond percolation threshold values have been determined for several numbers of two (2D) and three (3D) dimensional lattices. In order to investigate the effect of the anisotropy in the exchange interaction on the results obtained for the isotropic model, a detailed investigation has been made on a honeycomb lattice. Some interesting results, such as second order reentrant phenomena in the phase diagrams have been found. - Highlights: • Anisotropic quantum Heisenberg model with bond dilution investigated. • Bond percolation threshold values given for 2D and 3D lattices in isotropic case. • Phase diagrams and ground state magnetizations investigated in detail. • Variation of the bond percolation threshold values with anisotropy determined.

  14. Phase diagrams of diluted transverse Ising nanowire

    Energy Technology Data Exchange (ETDEWEB)

    Bouhou, S.; Essaoudi, I. [Laboratoire de Physique des Matériaux et Modélisation, des Systèmes, (LP2MS), Unité Associée au CNRST-URAC 08, University of Moulay Ismail, Physics Department, Faculty of Sciences, B.P. 11201 Meknes (Morocco); Ainane, A., E-mail: ainane@pks.mpg.de [Laboratoire de Physique des Matériaux et Modélisation, des Systèmes, (LP2MS), Unité Associée au CNRST-URAC 08, University of Moulay Ismail, Physics Department, Faculty of Sciences, B.P. 11201 Meknes (Morocco); Max-Planck-Institut für Physik Complexer Systeme, Nöthnitzer Str. 38 D-01187 Dresden (Germany); Saber, M. [Laboratoire de Physique des Matériaux et Modélisation, des Systèmes, (LP2MS), Unité Associée au CNRST-URAC 08, University of Moulay Ismail, Physics Department, Faculty of Sciences, B.P. 11201 Meknes (Morocco); Max-Planck-Institut für Physik Complexer Systeme, Nöthnitzer Str. 38 D-01187 Dresden (Germany); Ahuja, R. [Condensed Matter Theory Group, Department of Physics and Astronomy, Uppsala University, 75120 Uppsala (Sweden); Dujardin, F. [Laboratoire de Chimie et Physique des Milieux Complexes (LCPMC), Institut de Chimie, Physique et Matériaux (ICPM), 1 Bd. Arago, 57070 Metz (France)

    2013-06-15

    In this paper, the phase diagrams of diluted Ising nanowire consisting of core and surface shell coupling by J{sub cs} exchange interaction are studied using the effective field theory with a probability distribution technique, in the presence of transverse fields in the core and in the surface shell. We find a number of characteristic phenomena. In particular, the effect of concentration c of magnetic atoms, the exchange interaction core/shell, the exchange in surface and the transverse fields in core and in surface shell of phase diagrams are investigated. - Highlights: ► We use the EFT to investigate the phase diagrams of Ising transverse nanowire. ► Ferrimagnetic and ferromagnetic cases are investigated. ► The effects of the dilution and the transverse fields in core and shell are studied. ► Behavior of the transition temperature with the exchange interaction is given.

  15. SALT for Language Acquisition.

    Science.gov (United States)

    Bancroft, W. Jane

    1996-01-01

    Discusses Schuster's Suggestive-Accelerative Learning Techniques (SALT) Method, which combines Lozanov's Suggestopedia with such American methods as Asher's Total Physical Response and Galyean's Confluent Education. The article argues that students trained with the SALT Method have higher achievement scores and better attitudes than others. (14…

  16. Hydroxycarboxylic acids and salts

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-02-24

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

  17. SALT for Language Acquisition.

    Science.gov (United States)

    Bancroft, W. Jane

    1996-01-01

    Discusses Schuster's Suggestive-Accelerative Learning Techniques (SALT) Method, which combines Lozanov's Suggestopedia with such American methods as Asher's Total Physical Response and Galyean's Confluent Education. The article argues that students trained with the SALT Method have higher achievement scores and better attitudes than others. (14…

  18. L-Edge X-ray Absorption Spectroscopy of Dilute Systems Relevant to Metalloproteins Using an X-ray Free-Electron Laser

    NARCIS (Netherlands)

    Mitzner, Rolf; Rehanek, Jens; Kern, Jan; Gul, Sheraz; Hattne, Johan; Taguchi, Taketo; Alonso-Mori, Roberto; Tran, Rosalie; Weniger, Christian; Schroeder, Henning; Quevedo, Wilson; Laksmono, Hartawan; Sierra, Raymond G.; Han, Guangye; Lassalle-Kaiser, Benedikt; Koroidov, Sergey; Kubicek, Katharina; Schreck, Simon; Kunnus, Kristjan; Brzhezinskaya, Maria; Firsov, Alexander; Minitti, Michael P.; Turner, Joshua J.; Moeller, Stefan; Sauter, Nicholas K.; Bogan, Michael J.; Nordlund, Dennis; Schlotter, William F.; Messinger, Johannes; Borovik, Andrew; Techert, Simone; de Groot, Frank M. F.; Foehlisch, Alexander; Erko, Alexei; Bergmann, Uwe; Yachandra, Vittal K.; Wernet, Philippe; Yano, Junko

    2013-01-01

    L-edge spectroscopy of 3d transition metals provides important electronic structure information and has been used in many fields. However, the use of this method for studying dilute aqueous systems, such as metalloenzymes, has not been prevalent because of severe radiation damage and the lack of sui

  19. Bond diluted Ising model in 2D

    Directory of Open Access Journals (Sweden)

    Bouamrane Rachid

    2013-03-01

    Full Text Available The bond diluted Ising model is studied by Monte Carlo method. The simulation is carried out on a two dimensional square lattice with missing bonds and free boundary conditions. The aim of this work is to investigate the thermodynamical properties of this model for different disorder degree parameter σ. The critical temperature is determined from the Binder cumulant and is shown to decreases as the disorder parameter σ increases linearly.

  20. Water Metabolism of Walruses by Isotope Dilution

    DEFF Research Database (Denmark)

    Acquarone, M.; Born, E. W.; Chwalibog, A.;

    In August 2000, the hydrogen isotope dilution method was used on 7 adult male Atlantic walruses (Odobenus rosmarus rosmarus) (weight: 1197±148 kg, mean±SD, range 1013-1508 kg) at a terrestrial haul-out in Northeastern Greenland to determine their body water pool sizes and body water turnover rate...... successfully be used on walruses to estimate water metabolism as well as other metabolic parameters....

  1. Geomechanics of bedded salt

    Energy Technology Data Exchange (ETDEWEB)

    Serata, S.; Milnor, S.W.

    1979-06-08

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

  2. Salt Tolerance in Soybean

    Institute of Scientific and Technical Information of China (English)

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

    2008-01-01

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

  3. Salt and nephrolithiasis.

    Science.gov (United States)

    Ticinesi, Andrea; Nouvenne, Antonio; Maalouf, Naim M; Borghi, Loris; Meschi, Tiziana

    2016-01-01

    Dietary sodium chloride intake is nowadays globally known as one of the major threats for cardiovascular health. However, there is also important evidence that it may influence idiopathic calcium nephrolithiasis onset and recurrence. Higher salt intake has been associated with hypercalciuria and hypocitraturia, which are major risk factors for calcium stone formation. Dietary salt restriction can be an effective means for secondary prevention of nephrolithiasis as well. Thus in this paper, we review the complex relationship between salt and nephrolithiasis, pointing out the difference between dietary sodium and salt intake and the best methods to assess them, highlighting the main findings of epidemiologic, laboratory and intervention studies and focusing on open issues such as the role of dietary salt in secondary causes of nephrolithiasis.

  4. Dilution physics modeling: Dissolution/precipitation chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Onishi, Y.; Reid, H.C.; Trent, D.S.

    1995-09-01

    This report documents progress made to date on integrating dilution/precipitation chemistry and new physical models into the TEMPEST thermal-hydraulics computer code. Implementation of dissolution/precipitation chemistry models is necessary for predicting nonhomogeneous, time-dependent, physical/chemical behavior of tank wastes with and without a variety of possible engineered remediation and mitigation activities. Such behavior includes chemical reactions, gas retention, solids resuspension, solids dissolution and generation, solids settling/rising, and convective motion of physical and chemical species. Thus this model development is important from the standpoint of predicting the consequences of various engineered activities, such as mitigation by dilution, retrieval, or pretreatment, that can affect safe operations. The integration of a dissolution/precipitation chemistry module allows the various phase species concentrations to enter into the physical calculations that affect the TEMPEST hydrodynamic flow calculations. The yield strength model of non-Newtonian sludge correlates yield to a power function of solids concentration. Likewise, shear stress is concentration-dependent, and the dissolution/precipitation chemistry calculations develop the species concentration evolution that produces fluid flow resistance changes. Dilution of waste with pure water, molar concentrations of sodium hydroxide, and other chemical streams can be analyzed for the reactive species changes and hydrodynamic flow characteristics.

  5. Atomic displacements in bcc dilute alloys

    Indian Academy of Sciences (India)

    Hitesh Sharma; S Prakash

    2007-04-01

    We present here a systematic investigation of the atomic displacements in bcc transition metal (TM) dilute alloys. We have calculated the atomic displacements in bcc (V, Cr, Fe, Nb, Mo, Ta and W) transition metals (TMs) due to 3d, 4d and 5d TMs at the substitutional site using the Kanzaki lattice static method. Wills and Harrison interatomic potential is used to calculate the atomic force constants, the dynamical matrix and the impurity-induced forces. We have thoroughly investigated the atomic displacements using impurities from 3d, 4d and 5d series in the same host metal and the same impurity in different hosts. We have observed a systematic pattern in the atomic displacements for Cr-, Fe-, Nb-, Mo-, Ta- and W-based dilute alloys. The atomic displacements are found to increase with increase in the number of d electrons for all alloys considered except for V dilute alloys. The 3d impurities are found to be more easily dissolved in the 3d host metals than 4d or 5d TMs whereas 4d and 5d impurities show more solubility in 4d and 5d TMs. In general, the relaxation energy calculation suggests that impurities may be easily solvable in 5d TM hosts when compared to 3d or 4d TMs.

  6. Infiltration as Ventilation: Weather-Induced Dilution

    Energy Technology Data Exchange (ETDEWEB)

    Sherman, Max H. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Turner, William J.N. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Walker, Iain S. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)

    2011-06-01

    The purpose of outdoor air ventilation is to dilute or remove indoor contaminants to which occupants are exposed. It can be provided by mechanical or natural means. In most homes, especially older homes, weather-driven infiltration provides the dominant fraction of the total ventilation. As we seek to provide good indoor air quality at minimum energy cost, it is important to neither over-ventilate nor under-ventilate. Thus, it becomes critically important to evaluate correctly the contribution infiltration makes to the total outdoor air ventilation rate. Because weather-driven infiltration is dependent on building air leakage and weather-induced pressure differences, a given amount of air leakage will provide different amounts of infiltration. Varying rates of infiltration will provide different levels of contaminant dilution and hence effective ventilation. This paper derives these interactions and then calculates the impact of weather-driven infiltration for different climates. A new “N-factor” is introduced to provide a convenient method for calculating the ventilation contribution of infiltration for over 1,000 locations across North America. The results of this work could be used in indoor air quality standards (specifically ASHRAE 62.2) to account for the contribution of weather-driven infiltration towards the dilution of indoor pollutants.

  7. Salt-specific stability and denaturation of a short salt-bridge forming alpha-helix

    CERN Document Server

    Dzubiella, Joachim

    2008-01-01

    The structure of a single alanine-based Ace-AEAAAKEAAAKA-Nme peptide in explicit aqueous electrolyte solutions (NaCl, KCl, NaI, and KF) at large salt concentrations (3-4 M) is investigated using 1 microsecond molecular dynamics (MD) computer simulations. The peptide displays 71 alpha-helical structure without salt and destabilizes with the addition of NaCl in agreement with experiments of a somewhat longer version. It is mainly stabilized by direct and indirect (i+4)EK salt bridges between the Lys and Glu side chains and a concomitant backbone shielding mechanism. NaI is found to be a stronger denaturant than NaCl, while the potassium salts hardly show influence. Investigation of the molecular structures reveals that consistent with recent experiments Na+ has a much stronger affinity to side chain carboxylates and backbone carbonyls than K+, thereby weakening salt bridges and secondary structure hydrogen bonds. At the same time the large I- has a considerable affinity to the nonpolar alanine in line with rece...

  8. Development of a salt drug with improved solubility: Ethionamide nitrate

    Science.gov (United States)

    Diniz, Luan F.; Carvalho, Paulo S.; de Melo, Cristiane C.; Ellena, Javier

    2017-06-01

    To avoid drug resistance, an adequate tuberculosis treatment should include not only a first-line drug but also at least one second-line drug such as, for example, Ethionamide (ETH). However, the dissolution rate and oral absorption of ETH is highly limited by its low aqueous solubility. Considering that a salt is in general more soluble than its parent compound, herein we depicted a new supramolecular modification of ETH, an Ethionamide nitrate salt (ETHNO3). This salt is the first ETH structure that has been crystallized with four independent ionic pairs (ETH+NO3-) in the asymmetric unit. In addition to the structural study, the salt formation was also identified on the FT-IR and FT-Raman spectra. The thermal behavior of ETHNO3 was also investigated here together with its solubility profile in three dissolution media (purified water, pH 4.0 and 7.0).

  9. Molecular analysis of two mouse dilute locus deletion mutations: Spontaneous dilute lethal20J and radiation-induced dilute prenatal lethal Aa2 alleles

    Energy Technology Data Exchange (ETDEWEB)

    Strobel, M.C.; Seperack, P.K.; Copeland, N.G.; Jenkins, N.A. (National Cancer Institute-Frederick Cancer Research Facility, MD (USA))

    1990-02-01

    The dilute (d) coat color locus of mouse chromosome 9 has been identified by more than 200 spontaneous and mutagen-induced recessive mutations. With the advent of molecular probes for this locus, the molecular lesion associated with different dilute alleles can be recognized and precisely defined. In this study, two dilute mutations, dilute-lethal20J (dl20J) and dilute prenatal lethal Aa2, have been examined. Using a dilute locus genomic probe in Southern blot analysis, we detected unique restriction fragments in dl20J and Aa2 DNA. Subsequent analysis of these fragments showed that they represented deletion breakpoint fusion fragments. DNA sequence analysis of each mutation-associated deletion breakpoint fusion fragment suggests that both genomic deletions were generated by nonhomologous recombination events. The spontaneous dl20J mutation is caused by an interstitial deletion that removes a single coding exon of the dilute gene. The correlation between this discrete deletion and the expression of all dilute-associated phenotypes in dl20J homozygotes defines the dl20J mutation as a functional null allele of the dilute gene. The radiation-induced Aa2 allele is a multilocus deletion that, by complementation analysis, affects both the dilute locus and the proximal prenatal lethal-3 (pl-3) functional unit. Molecular analysis of the Aa2 deletion breakpoint fusion fragment has provided access to a previously undefined gene proximal to d. Initial characterization of this new gene suggests that it may represent the genetically defined pl-3 functional unit.

  10. MIPs in Aqueous Environments.

    Science.gov (United States)

    Wan, Ying-chun; Ma, Hui-ting; Lu, Bin

    2015-01-01

    When organic solvent-compatible molecularly imprinted polymers (MIPs) are used in aqueous environment, how to reduce nonspecific binding is a major challenge. By modifying the binding solvents and introducing appropriate washing and elution steps, even relatively hydrophobic MIPs can gain optimal rebinding selectivity in aqueous conditions. Furthermore, water-compatible MIPs that can be used to treat aqueous samples directly have been prepared. The use of hydrophilic co-monomers, the controlled surface modification through controlled radical polymerization, and the new interfacial molecular imprinting methods are different strategies to prepare water-compatible MIPs. By combining MIPs with other techniques, both organic solvent-compatible and water-compatible MIPs can display better functional performances in aqueous conditions. Intensive studies on MIPs in aqueous conditions can provide new MIPs with much-improved compatibilities that will lead to more interesting applications in biomedicine and biotechnology.

  11. Effect of Protein-Lipid-Salt Interactions on Sodium Availability in the Mouth and Consequent Perception of Saltiness: In Solutions.

    Science.gov (United States)

    Yucel, Umut; Peterson, Devin G

    2015-09-01

    The influence of protein-sodium interactions on the availability of sodium in the aqueous phase of liquid samples and consequently on the perception of saltiness was investigated. The aqueous effluents of casein and casein emulsion-salt solutions were monitored for sodium availability from a tongue column system. In the aqueous protein-salt solutions, increasing the protein/salt ratio from 1:1 to 5:1 or 10:1 significantly decreased the initial salt concentration in the effluent and resulted in a higher salt concentration in the effluent over time. Sensory analysis was in agreement. Samples with increased protein were rated as having significantly lower initial saltiness and a higher salty aftertaste. However, when casein was formulated as an emulsion, the initial release of sodium in the effluent was enhanced (compared to nonemulsified protein). Increasing the emulsion interfacial area (more hydrophilic segments of the protein were structured into the aqueous phase) resulted in a higher salt concentration in the aqueous phase and greater perceived saltiness intensity. In summary, protein interactions, specifically ionic, were reported as food interactions that influence salt perception and provide a basis to develop higher flavor quality low-sodium food products.

  12. Crushed Salt Constitutive Model

    Energy Technology Data Exchange (ETDEWEB)

    Callahan, G.D.

    1999-02-01

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

  13. pH and electric conductivity study of H{sub 2}O/MEG/salt systems on monoethyleneglycol (MEG) reclamation units in gas processing; Estudo de pH e condutividade eletrica em sistemas H{sub 2}O/MEG/sal, em unidades de recuperacao de monoetilenoglicol (MEG), no processamento de gas natural

    Energy Technology Data Exchange (ETDEWEB)

    Senna, Camila; Carrijo, Darley; Nascimento, Jailton; Grava, Wilson [PETROBRAS, Rio de Janeiro, RJ (Brazil). Centro de Pesquisas (CENPES); Lemos, Alessandro A.; Andrade, Wander V.; Chiavone-Filho, Osvaldo; Amorim, Josinira Antunes de [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil). Dept. de Engenharia Quimica

    2008-07-01

    The monoethylene glycol (MEG) is injected in natural gas production wells in order to combine with the free water, altering the thermodynamic conditions for the formation of hydrates. The presence of MEG in aqueous solutions containing salts provokes the decrease of the solubility of the same ones. Information of properties as the pH and the conductivity are important for the control of the process. Before this, the present work has as objective determines the behavior of the aqueous solutions with MEG and NaCl in pH and conductivity terms, in different temperatures, with views to the stage of recovery of MEG and the salt precipitation beginning. The experimental methodology consisted of the elaboration of synthetic solutions of the mixtures in study, covering every MEG concentration range and temperature between 5 and 90 deg C. The conductivity results for the system H{sub 2}O+MEG showed that the conductivity decreases with the concentration of MEG and it increases with the temperature. A conductivity increase was observed for diluted concentrations of MEG, due to the most pronounced effect of protonation of MEG. For pH measures, it was necessary to develop a calibration procedure due to the fact that this property varies with the solvent media. The pH values decrease as it increases the concentration of MEG, reaching a value practically constant around 40%. (author)

  14. Gases in molten salts

    CERN Document Server

    Tomkins, RPT

    1991-01-01

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

  15. Mechanism of Pitting Corrosion Prevention by Nitrite in Carbon Steel Exposed to Dilute Salt Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Philip E. Zapp; John W. Van Zee

    2002-02-01

    The research has developed a broad fundamental understanding of the inhibition action of nitrite ions in preventing nitrate pitting corrosion of carbon steel tanks containing high-level radioactive waste. This fundamental understanding can be applied to specific situations during waste removal for permanent disposition and waste tank closure to ensure that the tanks are maintained safely. The results of the research provide the insight necessary to develop solutions that prevent further degradation.

  16. The Aggregation Behavior and Formation of Nanoparticles of Oleoylchitosan in Dilute Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    LI Yanyan; CHEN Xiguang; SUN Gangzheng; XING Ke

    2008-01-01

    Oleoylchitosans (O-chitosans) with different degrees of substitution (DS) were synthesized by reacting chitosan with oleoyl chloride. The chemical structures of the products were characterized by 1H NMR and FT-IR. These results suggested the for-mation of an amide linkage between the amino groups of chitosan and the carboxyl groups of oleic acid. The viscosity of O-chitosan sharply increased with the increase of concentration, whereas that of unmodified chitosan rose only slightly. This increase became larger as the DS increased. All of the O-chitosans could reduce surface tension slightly. The critical aggregation concentration (CAC) of O-chitosans with DS 5%, 11%, and 27% were 79.43 mgL-1, 31.6 mgL-1, and 10mgL-1, respectively. Nanoparticles were prepared using an O/W emulsification method. The mean diameters of the polymeric amphiphilic nanoparticles of O-chitosans with DS 5% and 11% were around 327.4 nm and 275.3 nm, respectively.

  17. Local structure of dilute aqueous DMSO solutions, as seen from molecular dynamics simulations

    Science.gov (United States)

    Idrissi, Abdenacer; Marekha, Bogdan A.; Barj, Mohammed; Miannay, François Alexandre; Takamuku, Toshiyuki; Raptis, Vasilios; Samios, Jannis; Jedlovszky, Pál

    2017-06-01

    The information about the structure of dimethyl sulfoxide (DMSO)-water mixtures at relatively low DMSO mole fractions is an important step in order to understand their cryoprotective properties as well as the solvation process of proteins and amino acids. Classical MD simulations, using the potential model combination that best reproduces the free energy of mixing of these compounds, are used to analyze the local structure of DMSO-water mixtures at DMSO mole fractions below 0.2. Significant changes in the local structure of DMSO are observed around the DMSO mole fraction of 0.1. The array of evidence, based on the cluster and the metric and topological parameters of the Voronoi polyhedra distributions, indicates that these changes are associated with the simultaneous increase of the number of DMSO-water and decrease of water-water hydrogen bonds with increasing DMSO concentration. The inversion between the dominance of these two types of H-bonds occurs around XDMSO = 0.1, above which the DMSO-DMSO interactions also start playing an important role. In other words, below the DMSO mole fraction of 0.1, DMSO molecules are mainly solvated by water molecules, while above it, their solvation shell consists of a mixture of water and DMSO. The trigonal, tetrahedral, and trigonal bipyramidal distributions of water shift to lower corresponding order parameter values indicating the loosening of these orientations. Adding DMSO does not affect the hydrogen bonding between a reference water molecule and its first neighbor hydrogen bonded water molecules, while it increases the bent hydrogen bond geometry involving the second ones. The close-packed local structure of the third, fourth, and fifth water neighbors also is reinforced. In accordance with previous theoretical and experimental data, the hydrogen bonding between water and the first, the second, and the third DMSO neighbors is stronger than that with its corresponding water neighbors. At a given DMSO mole fraction, the behavior of the intensity of the high orientational order parameter values indicates that water molecules are more ordered in the vicinity of the hydrophilic group while their structure is close-packed near the hydrophobic group of DMSO.

  18. The Interaction of Polycrystalline Copper Films with Dilute Aqueous Solutions of Cupric Chloride

    Science.gov (United States)

    1989-10-01

    in atmosphere has always been of interest because of the extensive use of copper and brass in buildings and statues, for example. A study by Pinnel et...solution and the sample surface layer have been reported with no mention of the microstructure of the copper sample except for a few cases where chemical...used as a substrate when the deposited film will be removed for mechanical testing. In this case , the copper film was removed prior to characterization

  19. Interaction Between Some Monosaccharides and Aspartic Acid in Dilute Aqueous Solutions

    Science.gov (United States)

    Kulikova, Galina A.

    2008-01-01

    Interaction between aspartic acid and d-glucose, d-galactose, and d-fructose has been studied by isothermal titration calorimetry, calorimetry of dissolution, and densimetry. It has been found that d-glucose and d-fructose form thermodynamically stable associates with aspartic acid, in contrast to d-galactose. The selectivity in the interaction of aspartic acid with monosaccharides is affected by their stereochemical structures. PMID:19669542

  20. Biological Recovery of Platinum Complexes from Diluted Aqueous Streams by Axenic Cultures

    Science.gov (United States)

    Maes, Synthia; Props, Ruben; Fitts, Jeffrey P.; De Smet, Rebecca; Vanhaecke, Frank; Boon, Nico; Hennebel, Tom

    2017-01-01

    The widespread use of platinum in high-tech and catalytic applications has led to the production of diverse Pt loaded wastewaters. Effective recovery strategies are needed for the treatment of low concentrated waste streams to prevent pollution and to stimulate recovery of this precious resource. The biological recovery of five common environmental Pt-complexes was studied under acidic conditions; the chloro-complexes PtCl42- and PtCl62-, the amine-complex Pt(NH3)4Cl2 and the pharmaceutical complexes cisplatin and carboplatin. Five bacterial species were screened on their platinum recovery potential; the Gram-negative species Shewanella oneidensis MR-1, Cupriavidus metallidurans CH34, Geobacter metallireducens, and Pseudomonas stutzeri, and the Gram-positive species Bacillus toyonensis. Overall, PtCl42- and PtCl62- were completely recovered by all bacterial species while only S. oneidensis and C. metallidurans were able to recover cisplatin quantitatively (99%), all in the presence of H2 as electron donor at pH 2. Carboplatin was only partly recovered (max. 25% at pH 7), whereas no recovery was observed in the case of the Pt-tetraamine complex. Transmission electron microscopy (TEM) revealed the presence of both intra- and extracellular platinum particles. Flow cytometry based microbial viability assessment demonstrated the decrease in number of intact bacterial cells during platinum reduction and indicated C. metallidurans to be the most resistant species. This study showed the effective and complete biological recovery of three common Pt-complexes, and estimated the fate and transport of the Pt-complexes in wastewater treatment plants and the natural environment. PMID:28046131

  1. Perchlorate, iodine supplements, iodized salt and breast milk iodine content

    Energy Technology Data Exchange (ETDEWEB)

    Kirk, Andrea B. [Department of Epidemiology, School of Public Health, University of North Texas Health Sciences Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107 (United States); Kroll, Martina; Dyke, Jason V.; Ohira, Shin-Ichi; Dias, Rukshan A.; Dasgupta, Purnendu K. [Department of Chemistry and Biochemistry, 700 Planetarium Place, University of Texas at Arlington, Arlington, TX 76019 (United States)

    2012-03-15

    This study was undertaken to determine if increasing maternal iodine intake through single dose tablets will decrease breast milk concentrations of the iodine-uptake inhibitor, perchlorate, through competitive inhibition. We also sought to determine if the timing of supplementation influences the fraction of iodine excreted in milk versus urine and to compare the effectiveness of iodized salt as a means of providing iodine to breastfed infants. Thirteen women who did not use supplements, seven of whom used iodized salt and six of whom used non-iodized salt, submitted four milk samples and a 24-h urine collection daily for three days. Women repeated the sampling protocol for three more days during which {approx} 150 {mu}g of iodine were taken in the evening and again for three days with morning supplementation. Samples were analyzed using isotope-dilution inductively-coupled plasma-mass spectrometry for iodine and isotope-dilution ion chromatography-tandem mass spectrometry for perchlorate. No statistically significant differences were observed in milk iodine or perchlorate concentrations during the two treatment periods. Estimated perchlorate intake was above the U.S. National Academy of Sciences suggested reference dose for most infants. Single daily dose iodine supplementation was not effective in decreasing milk perchlorate concentrations. Users of iodized salt had significantly higher iodine levels in milk than non-users. Iodized salt may be a more effective means of iodine supplementation than tablets. - Highlights: Black-Right-Pointing-Pointer Estimated infant exposures to perchlorate were, on a {mu}g/kg basis, {approx} 5 Multiplication-Sign higher than those of mothers. Black-Right-Pointing-Pointer Daily supplements are less effective than iodized salt in providing iodine to lactating women. Black-Right-Pointing-Pointer Low iodine and high perchlorate in milk may place infants at risk of iodine deficiency.

  2. Thermodynamic studies of aqueous solutions of 2,2,2-cryptand at 298.15 K: enthalpy-entropy compensation, partial entropies, and complexation with K+ ions.

    Science.gov (United States)

    Shaikh, Vasim R; Terdale, Santosh S; Ahamad, Abdul; Gupta, Gaurav R; Dagade, Dilip H; Hundiwale, Dilip G; Patil, Kesharsingh J

    2013-12-19

    The osmotic coefficient measurements for binary aqueous solutions of 2,2,2-cryptand (4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8] hexacosane) in the concentration range of ~0.009 to ~0.24 mol·kg(-1) and in ternary aqueous solutions containing a fixed concentration of 2,2,2-cryptand of ~0.1 mol·kg(-1) with varying concentration of KBr (~0.06 to ~0.16 mol·kg(-1)) have been reported at 298.15 K. The diamine gets hydrolyzed in aqueous solutions and needs proper approach to obtain meaningful thermodynamic properties. The measured osmotic coefficient values are corrected for hydrolysis and are used to determine the solvent activity and mean ionic activity coefficients of solute as a function of concentration. Strong ion-pair formation is observed, and the ion-pair dissociation constant for the species [CrptH](+)[OH(-)] is reported. The excess and mixing thermodynamic properties (Gibbs free energy, enthalpy, and entropy changes) have been obtained using the activity data from this study and the heat data reported in the literature. Further, the data are utilized to compute the partial molal entropies of solvent and solute at finite as well as infinite dilution of 2,2,2-cryptand in water. The concentration dependent non-linear enthalpy-entropy compensation effect has been observed for the studied system, and the compensation temperature along with entropic parameter are reported. Using solute activity coefficient data in ternary solutions, the transfer Gibbs free energies for transfer of the cryptand from water to aqueous KBr as well as transfer of KBr from water to aqueous cryptand were obtained and utilized to obtain the salting constant (ks) and thermodynamic equilibrium constant (log K) values for the complex (2,2,2-cryptand:K(+)) at 298.15 K. The value of log K = 5.8 ± 0.1 obtained in this work is found to be in good agreement with that reported by Lehn and Sauvage. The standard molar entropy for complexation is also estimated for the 2,2,2-cryptand

  3. Combustion of hythane diluted with CO2

    Directory of Open Access Journals (Sweden)

    Hraiech Ibtissem

    2015-01-01

    Full Text Available With increasing concern about energy shortage and environmental protection, improving engine fuel economy and reducing exhaust emissions have become major research topics in combustion and engine development. Hythane (a blend of hydrogen H2 and natural gas NG has generated a significant interest as an alternative fuel for the future. This paper describes an experimental study of the effects of CO2 addition on the stability of a turbulent jet diffusion NG-H2 flame. The mole fraction of hydrogen (% H2 in NG-H2 mixture was varied from 0% to 50%. The equivalence ratio of the hythane/CO2/air mixture was kept at stoichiometry. The results show that the lift-off height increases with the addition of CO2 at various % H2 content in hythane. However, we observe that with 20% H2, we can obtain a stable flame diluted with 40% CO2, while for 0% H2, the flame is blown out above 20% CO2. This means that the limits of flame blowing out are pushed with the additions of H2. Moreover, the results show that for %H2 content in NG-H2 fuel up to 10%, the addition of CO2 could produce lifted flame if the % CO2 is low. At higher % CO2 dilution, flame would remain attached until blow-out. This is mainly due to the fact that the dilution leads to ejection velocities very high but reactivity of the mixture does not change so the flame tends to stretch.

  4. Experimental measurement and modeling of the distribution of solvent and ions between an aqueous phase and an ion exchange resin

    DEFF Research Database (Denmark)

    Christensen, Søren Gregers; Thomsen, Kaj

    2005-01-01

    The distribution of solutes and solvent between an aqueous solution of salt and an ion exchange resin has been measured at ambient temperature. The experiments have been performed for aqueous solutions of KNO3, KCl, Ca(NO3)2 and CaCl2 in the concentration range of 0-3N. The absorption has been...

  5. Water Metabolism of Walruses by Isotope Dilution

    DEFF Research Database (Denmark)

    Acquarone, M.; Born, E. W.; Chwalibog, A.

    In August 2000, the hydrogen isotope dilution method was used on 7 adult male Atlantic walruses (Odobenus rosmarus rosmarus) (weight: 1197±148 kg, mean±SD, range 1013-1508 kg) at a terrestrial haul-out in Northeastern Greenland to determine their body water pool sizes and body water turnover rates...... was sampled via an epidural catheter, at regular intervals, for up to seven hours after the initial enrichment to assess isotope equilibration in the body water pools. Five individuals returned to the haul-out after feeding trips of varying duration (158±86 hr, 44-287 hr) where they were immobilized again...

  6. Characterization of nanoparticles in diluted clear solutions for Silicalite-1 zeolite synthesis using liquid 29Si NMR, SAXS and DLS.

    Science.gov (United States)

    Follens, L R A; Aerts, A; Haouas, M; Caremans, T P; Loppinet, B; Goderis, B; Vermant, J; Taulelle, F; Martens, J A; Kirschhock, C E A

    2008-09-28

    Clear solutions for colloidal Silicalite-1 synthesis were prepared by reacting tetraethylorthosilicate in aqueous tetrapropylammonium hydroxide solution. A dilution series with water resulting in clear solutions with a TEOS ratio TPAOH ratio H2O molar ratio of 25 : 9 : 152 up to 25 : 9 : 15,000 was analysed using liquid 29Si nuclear magnetic resonance (NMR), synchrotron small angle X-ray scattering (SAXS) and dynamic light scattering (DLS). Particle sizes were derived independently from DLS and from the combination of SAXS and NMR. NMR allowed quantitative characterization of silicon distributed over nanoparticles and dissolved oligomeric silicate polyanions. In all samples studied, the majority of silicon (78-90%) was incorporated in the nanoparticle fraction. In concentrated suspensions, silicate oligomers were mostly double-ring species (D3R, D4R, D5R, D6R). Dilution with water caused their depolymerisation. Contrarily, the internal condensation and size of nanoparticles increased with increasing dilution. SAXS revealed a decrease of effective nanoparticle surface charge upon dilution, reducing the effective particle interactions. With DLS, the reduction of nanoparticle interactions could be confirmed monitoring the collective diffusion mode. The observed evolution of nanoparticle characteristics provides insight in the acceleration of the Silicalite-1 crystallization upon dilution, in view of different crystallization models proposed in the literature.

  7. Optical techniques for nanoscale probing and chemical detection in aqueous environments

    Science.gov (United States)

    Pristinski, Denis

    We present an investigation of charge-dependent physical properties of water-soluble synthetic polymers and polymer-based layered structures, using optical detection methods in a visible range. We apply in situ nanoscale optical techniques to study response of polymer systems to changes in pH, polymer concentration, and concentration and type of counterions. This work describes three optical techniques and custom built instrumental setups for nanoscale polymer characterization in aqueous environment. Phase-modulated ellipsometry was applied to determine the refraction coefficient and the thickness of a hydrogel-like polymer layer on a substrate. The present study describes the sensitivity of the phase modulated ellipsometry to errors of measurement and determines conditions for decoupling film thickness and refraction index. It is shown that, for a certain range of film thickness, both the thickness and the refractive index can be determined from a single measurement with high precision. This optimal range of the film thickness is calculated for organic thin films, and the analysis is tested on crosslinked poly(methacrylic acid) polymer films in air and in water. Fluorescent correlation spectroscopy was used to investigate diffusion of a synthetic polyelectrolyte in aqueous solutions. Translational diffusion of Alexa-labeled poly(methacrylic acid) chains was studied in very dilute, 10-4 mg/ml, solutions as a function of polymer charge density and counterion concentration. The results illustrate the utility of the technique for studying hydrodynamic sizes of polyelectrolyte coils in response to variation in solution pH or concentration of salt and polyelectrolytes. We apply surface-enhanced Raman scattering (SERS) for studying of enhancement capabilities of individual silver nanoparticles attached to glass and silicon substrates. Nanoparticles were electrostatically bound to a self-assembled polyallylamine hydrochloride (PAH) monolayer, which was deposited on

  8. Salting-out and salting-in: competitive effects of salt on the aggregation behavior of soy protein particles and their emulsifying properties.

    Science.gov (United States)

    Xu, Hua-Neng; Liu, Yang; Zhang, Lianfu

    2015-08-01

    Emulsions stabilized by protein particles have gained increasing research attention due to their combined advantages of biocompatibility and superior stability. In this study, colloidal particles consisting of soy protein isolates (SPIs) prepared through a heat-treatment procedure are used to make oil-in-water emulsions at a protein concentration of 10 g L(-1) and a pH of 5.91. We investigate parallelly the effects of NaCl on the stability and rheological properties of the particle suspensions and their stabilized emulsions at salt concentrations of 0, 100 and 400 mM. The aggregation behavior of the particles is strongly dependent on the NaCl concentration, showing signs of sedimentation at low NaCl concentration (100 mM) but redispersion again at high NaCl concentration (400 mM). The extensive particle aggregation is beneficial to the formation of a continuous interfacial film for the emulsions, and hence results in a remarkable increase of creaming stability and interfacial viscoelastic moduli. The results can be explained in terms of two competitive effects of NaCl: salting-out and salting-in, which are attributed to complex electrostatic interactions between the particles as a function of NaCl concentration. The delicate balance between salting-out and salting-in provides an interesting insight into the nature of underlying protein particle interactions in aqueous suspensions and a possible mechanism for tailoring their emulsifying properties via salt effects.

  9. Salt Pomo: An Ethnogeography

    OpenAIRE

    McCarthy, Helen

    1986-01-01

    Recent research in Salt Pomo territory has produced new ethnogeographic data to add to the named villages identified in much earlier studies (Barrett 1904, 1908; Merriam MS, 1966, 1977). This new information is of particular interest because it significantly increases our general knowledge of the Salt Pomo, about whom little is otherwise known, and because it contributes to an understanding of their settlement pattern as well as to broader, regional land-use analyses. In addition, the study a...

  10. Aqueous SARA ATRP using Inorganic Sulfites.

    Science.gov (United States)

    Abreu, Carlos M R; Fu, Liye; Carmali, Sheiliza; Serra, Arménio C; Matyjaszewski, Krzysztof; Coelho, Jorge F J

    2017-01-14

    Aqueous supplemental activator and reducing agent atom transfer radical polymerization (SARA ATRP) using inorganic sulfites was successfully carried out for the first time. Under optimized conditions, a well-controlled poly[oligo(ethylene oxide) methyl ether acrylate] (POEOA) was obtained with sulfites (e.g. Na2S2O4) were continuously fed into the reaction mixture. The mechanistic studies proved that these salts can activate alkyl halides directly and regenerate the activator complex. The effects of the feeding rate of the SARA agent (inorganic sulfites), ligand and its concentration, halide salt and its concentration, sulfite used, and copper concentration, were systematically studied to afford fast polymerizations rates while maintaining the control over polymerization. The kinetic data showed linear first-order kinetics, linear evolution of molecular weights with conversion, and polymers with narrow molecular weight distributions (Đ ~1.2) during polymerization even at relatively high monomer conversions (~80%). "One-pot" chain extension and "one-pot" block copolymerization experiments proved the high chain-end functionality. The polymerization could be directly regulated by starting or stopping the continuous feeding of the SARA agent. Under biologically relevant conditions, the aqueous SARA ATRP using inorganic sulfites was used to synthesize a well-defined protein-polymer hybrid by grafting of P(OEOA480) from BSA-O-[iBBr]30.

  11. Thermodynamic Properties of 1:1 Salt Aqueous Solutions with the Electrolattice Equation of State Propriétés thermophysiques des solutions aqueuses de sels 1:1 avec l’équation d’état de réseau pour électrolytes

    Directory of Open Access Journals (Sweden)

    Zuber A.

    2013-05-01

    Full Text Available The electrolattice Equation of State (EOS is a model that extends the MattediTavares-Castier EOS (MTC EOS to systems with electrolytes. This model considers the effect of three terms. The first one is based on a lattice-hole model that considers local composition effects derived in the context of the generalized Van der Waals theory: the MTC EOS was chosen for this term. The second and the third terms are the Born and the MSA contributions, which take into account ion charging and discharging and long-range ionic interactions, respectively. Depending only on two energy interaction parameters, the model represents satisfactorily the vapor pressure and the mean ionic activity coefficient data of single aqueous solutions containing LiCI, LiBr, LiI, NaCl, NaBr, NaI, KCl, KBr, KI, CsCl, CsBr, CsI, or RbCI. Two methods are presented and contrasted: the salt-specific and the ion-specific approaches. Therefore, the aim of this work is to calculate thermodynamic properties that are extensively used to design, operate and optimize many industrial processes, including water desalination. L’équation d’état, dite électrolattice, est un modèle qui étend l’équation d’état de Mattedi-Tavares-Castier à des systèmes avec électrolytes. Ce modèle prend en compte l’effet de trois termes. Le premier terme est basé sur les trous dans le réseau en considérant les effets de la composition locale, étude effectuée dans le cadre de la théorie généralisée de Van der Waals : l’équation d’état de Mattedi-Tavares-Castier a été choisie pour ce premier terme. Les deuxième et troisième termes sont les contributions de Born et du MSA. Ils tiennent compte du chargement et du déchargement des ions, et des interactions ioniques à longue distance, respectivement. Le modèle n’ayant besoin que de deux paramètres d’interaction énergétique, il modélise de manière satisfaisante la pression de vapeur et le coefficient d’activité ionique

  12. Hygroscopic Salts on Mars

    Science.gov (United States)

    Melchiorri, R.; Davila, A. F.; Chittenden, J.; Haberle, R. M.

    2008-12-01

    We present preliminary results on the influence of a salt-rich regolith in the water cycle of Mars. Global climate modeling shows that the relative humidity on the Martian surface often reaches values above the deliquescence point of salts that are common components of the regolith. At the deliquescence point, these salts will absorb atmospheric water vapor and form a saturated, transient liquid solution that is stable under a range of temperatures. If atmospheric temperatures fall below the eutectic point of the solution, the later will freeze in the pore space of the regolith, thereby resulting in a net transport of water from the vapor phase in the atmosphere, to the solid state in the regolith. This simple model partially accounts for some the distribution of water on the Martian surface as revealed by Mars Odyssey, in particular, we find that: even though the Cl and surface water distributions detected by HEND/ODYSSEY are highly correlated, salt deliquescence under the the present atmospheric conditions does not explain the overall distribution of water in the near surface regolith. However deliquescence of salt-rich soils could be an important contributor to the distribution of water in the regolith at high obliquity. In that scenario the water in the near-surface regolith would be the remnant of high obliquity conditions salt deliquescence is still active in different regions on Mars today, and it should be introduced as a parameter in the modern GCMs as a new ground/atmosphere interaction

  13. Analysis of Abnormal Phenomena in High Magnesium Boron Containing Salt Brine System%高镁含硼盐卤体系反常现象解析

    Institute of Scientific and Technical Information of China (English)

    乌志明; 崔香梅; 郑绵平

    2012-01-01

    Such phenomena as "supersaturated solubility", "salt formation by dilution" and "solubility increase of homonymy ion" exist in high magnesium boron containing salt brine system. Our research indicates that the magnesium chloride solution is neutral with medium or low concentration. It shows acidic property with high concentration and the pH value is lower than 4.5 when saturated. But many types of magnesium borate minerals are alkaline ones with pH value higher than 8.0. We know in general acid and base could hardly co-exist in an aqueous solution, but magnesium borate and magnesium chloride in high magnesium boron containing salt brine system do owing to the possession of the homonymy ion. The above mentioned abnormal phenomena can be satisfactorily interpreted with special acidity change of magnesium chloride solution and some related phase chemistry data.%高镁含硼盐卤体系中存在“过饱和溶解度”、“稀释成盐”和同名离子“增溶”等反常现象.研究发现:氯化镁溶液在中低浓度时显中性,在高浓度时显酸性,饱和时pH值小于4.5.而各种镁硼酸盐基本都是pH值大于8.0的碱性矿物.水溶液中酸碱难共存,但镁硼酸盐与氯化镁却因具有相同离子而能够在高镁含硼盐卤体系中共存.结合氯化镁溶液特殊酸度变化规律与相关相化学数据可较圆满的解释高镁含硼盐卤体系中的反常现象.

  14. An Alternative Approach for Preparing and Standardizing Some Common Aqueous Reagents Used in an Undergraduate Laboratory

    Science.gov (United States)

    Melaku, Samuel; Dabke, Rajeev B.

    2014-01-01

    A guide for instructors and laboratory assistants to prepare some common aqueous reagents used in an undergraduate laboratory is presented. Dilute reagents consisting of H[superscript +](aq), I[subscript 3][superscript-](aq), Ce[superscript 4+](aq), and Ag[superscript+](aq) were prepared by electrolytic oxidation of respective precursors.…

  15. Study on aqueous two-phase systems of the mixture SDS/CTAB surfactants

    Institute of Scientific and Technical Information of China (English)

    LI Ying; CHEN Yah-ming; ZHAO Kong-shuang; Takumi HIKIDA

    2004-01-01

    The phenomenon of two dilute aqueous phases composed of sodium dodecylsulfate (SDS) and cetyltrimethyl ammonium bromide(CTAB) was investigated under various conditions such as concentrations and molarratios of the two surfactants, the addition of sodium chloride and temperature. Vesicles formation was found in theboth phases by TEM image.

  16. Microalgae growth on the aqueous phase from Hydrothermal Liquefaction of the same microalgae

    NARCIS (Netherlands)

    Garcia Alba, Laura; Torri, Cristian; Fabbri, Daniele; Kersten, Sascha R.A.; Brilman, Derk W.F. (Wim)

    2013-01-01

    Cultivation of Desmodesmus sp. microalgae in the recycled aqueous phase (AP) recovered after Hydrothermal Liquefaction (HTL) of the same microalgae was studied to evaluate the potential of nutrients recycling. AP dilution ratio was systematically varied, using either water or water enriched with sta

  17. Microalgae growth on the aqueous phase from Hydrothermal Liquefaction of the same microalgae

    NARCIS (Netherlands)

    Garcia Alba, Laura; Torri, Cristian; Fabbri, Daniele; Kersten, Sascha R.A.; Brilman, Derk Willem Frederik

    2013-01-01

    Cultivation of Desmodesmus sp. microalgae in the recycled aqueous phase (AP) recovered after Hydrothermal Liquefaction (HTL) of the same microalgae was studied to evaluate the potential of nutrients recycling. AP dilution ratio was systematically varied, using either water or water enriched with sta

  18. Microalgae growth on the aqueous phase from Hydrothermal Liquefaction of the same microalgae

    NARCIS (Netherlands)

    Garcia Alba, Laura; Torri, Cristian; Fabbri, Daniele; Kersten, Sascha R.A.; Brilman, Derk Willem Frederik

    2013-01-01

    Cultivation of Desmodesmus sp. microalgae in the recycled aqueous phase (AP) recovered after Hydrothermal Liquefaction (HTL) of the same microalgae was studied to evaluate the potential of nutrients recycling. AP dilution ratio was systematically varied, using either water or water enriched with

  19. Structural evolution of aqueous NaCl solutions dissolved in supercritical carbon dioxide under isobaric heating by mid and near infrared spectroscopy.

    Science.gov (United States)

    Oparin, R; Tassaing, T; Danten, Y; Besnard, M

    2005-03-01

    The local order in aqueous NaCl solutions diluted in supercritical carbon dioxide at constant pressure as a function of NaCl concentration and temperature has been investigated using near and mid infrared absorption spectroscopy. The near IR results have allowed us to estimate the water concentration in CO(2) rich phase, whereas the state of water aggregation in CO(2) phase was investigated using mid IR spectroscopy. The analysis of the band shape variations of the OD stretching mode of HOD led us to conclude that below 100 degrees C, water molecules dissolved in CO(2) exist only under their monomeric form, whatever the salt concentration is, whereas hydrogen-bonded species, namely, dimers start to appear at higher temperatures. Larger aggregates have a negligible concentration in the range of temperature-pressure investigated. Using near and mid infrared data, we have calculated the concentrations of water species in the CO(2) phase. Upon heating, it was found that the concentration of dimers considerably increases at the expense of the monomers and only dimers are detected in carbon dioxide at highest temperatures. Changing the salt concentration affects significantly the concentration of monomers and decreases strongly the dimers population as the solution becomes progressively saturated in salt. In the saturated solution, at 340 degrees C, the dimer concentration is at least two times smaller than in the binary water-CO(2) mixture. These findings are in qualitative agreement with existing thermodynamics data showing that addition of NaCl to the binary H(2)O-CO(2) system shifts the range of partial miscibility of water and CO(2) towards higher pressure and temperature.

  20. Aqueous lithium air batteries

    Energy Technology Data Exchange (ETDEWEB)

    Visco, Steven J.; Nimon, Yevgeniy S.; De Jonghe, Lutgard C.; Petrov, Alexei; Goncharenko, Nikolay

    2017-05-23

    Aqueous Li/Air secondary battery cells are configurable to achieve high energy density and prolonged cycle life. The cells include a protected a lithium metal or alloy anode and an aqueous catholyte in a cathode compartment. The aqueous catholyte comprises an evaporative-loss resistant and/or polyprotic active compound or active agent that partakes in the discharge reaction and effectuates cathode capacity for discharge in the acidic region. This leads to improved performance including one or more of increased specific energy, improved stability on open circuit, and prolonged cycle life, as well as various methods, including a method of operating an aqueous Li/Air cell to simultaneously achieve improved energy density and prolonged cycle life.

  1. Diluted Equilibrium Sterile Neutrino Dark Matter

    CERN Document Server

    Patwardhan, Amol V; Kishimoto, Chad T; Kusenko, Alexander

    2015-01-01

    We present a model where sterile neutrinos with rest masses in the range ~ keV to ~ MeV can be the dark matter and be consistent with all laboratory, cosmological, large scale structure, and X-ray constraints. These sterile neutrinos are assumed to freeze out of thermal and chemical equilibrium with matter and radiation in the very early universe, prior to an epoch of prodigious entropy generation ("dilution") from out-of-equilibrium decay of heavy particles. In this work, we consider heavy, entropy-producing particles in the ~ TeV to ~ EeV rest mass range, possibly associated with new physics at high energy scales. The process of dilution can give the sterile neutrinos the appropriate relic densities, but it also alters their energy spectra so that they could act like cold dark matter, despite relatively low rest masses as compared to conventional dark matter candidates. Moreover, since the model does not rely on active-sterile mixing for producing the relic density, the mixing angles can be small enough to ...

  2. Diluted equilibrium sterile neutrino dark matter

    Science.gov (United States)

    Patwardhan, Amol V.; Fuller, George M.; Kishimoto, Chad T.; Kusenko, Alexander

    2015-11-01

    We present a model where sterile neutrinos with rest masses in the range ˜keV to ˜MeV can be the dark matter and be consistent with all laboratory, cosmological, and large-scale structure, as well as x-ray constraints. These sterile neutrinos are assumed to freeze out of thermal and chemical equilibrium with matter and radiation in the very early Universe, prior to an epoch of prodigious entropy generation ("dilution") from out-of-equilibrium decay of heavy particles. In this work, we consider heavy, entropy-producing particles in the ˜TeV to ˜EeV rest-mass range, possibly associated with new physics at high-energy scales. The process of dilution can give the sterile neutrinos the appropriate relic densities, but it also alters their energy spectra so that they could act like cold dark matter, despite relatively low rest masses as compared to conventional dark matter candidates. Moreover, since the model does not rely on active-sterile mixing for producing the relic density, the mixing angles can be small enough to evade current x-ray or lifetime constraints. Nevertheless, we discuss how future x-ray observations, future lepton number constraints, and future observations and sophisticated simulations of large-scale structure could, in conjunction, provide evidence for this model and/or constrain and probe its parameters.

  3. Dilute Potts model in two dimensions.

    Science.gov (United States)

    Qian, Xiaofeng; Deng, Youjin; Blöte, Henk W J

    2005-11-01

    We study the two-dimensional dilute q-state Potts model by means of transfer-matrix and Monte Carlo methods. Using the random-cluster representation, we include noninteger values of q. We locate phase transitions in the three-dimensional parameter space of q, the Potts coupling K>0, and the chemical potential of the vacancies. The critical plane is found to contain a line of fixed points that divides into a critical branch and a tricritical one, just as predicted by the renormalization scenario formulated by Nienhuis et al for the dilute Potts model. The universal properties along the line of fixed points agree with the theoretical predictions. We also determine the density of the vacancies along these branches. For q=2-squareroot of 2 we obtain the phase diagram in a three-dimensional parameter space that also includes a coupling V> or = 0 between the vacancies. For q=2, the latter space contains the Blume-Capel model as a special case. We include a determination of the tricritical point of this model, as well as an analysis of percolation clusters constructed on tricritical Potts configurations for noninteger q. This percolation study is based on Monte Carlo algorithms that include local updates flipping between Potts sites and vacancies. The bond updates are performed locally for and by means of a cluster algorithm for q>1. The updates for q>1 use a number of operations per site independent of the system size.

  4. 40 CFR 1065.240 - Dilution air and diluted exhaust flow meters.

    Science.gov (United States)

    2010-07-01

    ... heat exchanger, either a CFV or a PDP will also function as a passive flow controller in a CVS system.... For any type of diluted exhaust flow meter, condition the flow as needed to prevent wakes, eddies... to at least 10 pipe diameters) or by using specially designed tubing bends, orifice plates or...

  5. Phase-transition and aggregation characteristics of a thermoresponsive dextran derivative in aqueous solutions.

    Science.gov (United States)

    Shi, Huan-Ying; Zhang, Li-Ming

    2006-10-16

    Grafting of poly(N-vinylcaprolactam) side chains onto a hydrophilic dextran backbone was found to provide the dextran with new, thermoresponsive properties in aqueous solutions. Depending on its solution concentration, the resulting dextran derivative could exhibit a temperature-induced phase-transition and critical transition temperature (T(c)). Different anions and cations of added salts, including five potassium salts and five alkali-metal chlorides, were observed to influence the T(c) value of its aqueous solution. Except for potassium iodide, all added salts were found to lower the T(c) value. The addition of the surfactant, cationic cetyltrimethylammonium bromide or anionic sodium dodecyl sulfate, resulted in an increase of the T(c) value. With the help of the Coomassie Brilliant Blue dye as a polarity probe, the formation of hydrophobic aggregates above the T(c) was revealed for this new dextran derivative in aqueous solution.

  6. Heterogeneous reactions of HOI, ICl and IBr on sea salt and sea salt proxies.

    Science.gov (United States)

    Braban, C F; Adams, J W; Rodriguez, D; Cox, R A; Crowley, J N; Schuster, G

    2007-06-28

    The heterogeneous chemistry of HOI, ICl and IBr on sea salt and sea salt proxies has been studied at 274 K using two experimental approaches: a wetted wall flow tube coupled to an electron impact mass spectrometer (WWFT-MS) and an aerosol flow tube (AFT) coupled to a differential mobility analyser (DMA) and a chemical ionisation mass spectrometer (CIMS). Uptake of all three title molecules into bulk aqueous halide salt films was rapid and controlled by gas phase diffusion. Uptake of HOI gave rise to gas-phase ICl and IBr, with the latter being the predominant product whenever Br(-) was present. Only partial release of IBr was observed due to high solubility of dihalogens in the film. ICl uptake gave the same yield of IBr as HOI uptake. Uptake of ICl on NaBr aerosol was accommodation limited with alpha = 0.018 +/- 0.004 and gas phase IBr product has a yield of 0.6 +/- 0.3. The results show that HOI can act as a catalyst for activation of bromine from sea-salt aerosols in the marine boundary layer, via the reactions: HOI(aq) + Cl + H--> ICl(aq) + H(2)O(l) and ICl(aq) + Br--> IBr(aq) + Cl.

  7. Origin of salt giants in abyssal serpentinite systems

    Science.gov (United States)

    Scribano, Vittorio; Carbone, Serafina; Manuella, Fabio C.; Hovland, Martin; Rueslåtten, Håkon; Johnsen, Hans-K.

    2017-03-01

    Worldwide marine salt deposits ranging over the entire geological record are generally considered climate-related evaporites, derived from the precipitation of salts (mainly chlorides and sulfates) from saturated solutions driven by solar evaporation of seawater. This explanation may be realistic for a salt thickness ≤100 m, being therefore inadequate for thicker (>1 km) deposits. Moreover, sub-seafloor salt deposits in deep marine basins are difficult to reconcile with a surface evaporation model. Marine geology reports on abyssal serpentinite systems provide an alternative explanation for some salt deposits. Seawater-driven serpentinization consumes water and increases the salinity of the associated aqueous brines. Brines can be trapped in fractures and cavities in serpentinites and the surrounding `country' rocks. Successive thermal dehydration of buried serpentinites can mobilize and accumulate the brines, forming highly saline hydrothermal solutions. These can migrate upwards and erupt onto the seafloor as saline geysers, which may form salt-saturated water pools, as are currently observed in numerous deeps in the Red Sea and elsewhere. The drainage of deep-seated saline brines to seafloor may be a long-lasting, effective process, mainly occurring in areas characterized by strong tectonic stresses and/or igneous intrusions. Alternatively, brines could be slowly expelled from fractured serpentinites by buoyancy gradients and, hence, separated salts/brines could intrude vertically into surrounding rocks, forming salt diapirs. Serpentinization is an ubiquitous, exothermic, long-lasting process which can modify large volumes of oceanic lithosphere over geological times. Therefore, buried salt deposits in many areas of the world can be reasonably related to serpentinites.

  8. Characterization of the Dilute Ising Antiferromagnet

    Energy Technology Data Exchange (ETDEWEB)

    Wiener, T.

    2000-09-12

    A spin glass is a magnetic ground state in which ferromagnetic and antiferromagnetic exchange interactions compete, thereby creating frustration and a multidegenerate state with no long range order. An Ising system is a system where the spins are constrained to lie parallel or antiparallel to a primary axis. There has been much theoretical interest in the past ten years in the effects of applying a magnetic field transverse to the primary axis in an Ising spin glass at low temperatures and thus study phase transitions at the T=0 limit. The focus of this study is to search for and characterize a new Ising spin glass system. This is accomplished by site diluting yttrium for terbium in the crystalline material TbNi{sub 2}Ge{sub 2}. The first part of this work gives a brief overview of the physics of rare earth magnetism and an overview of experimental characteristics of spin glasses. This is followed by the methodology used to manufacture the large single crystals used in this study, as well as the measurement techniques used. Next, a summary of the results of magnetic measurements on across the dilution series from pure terbium to pure yttrium is presented. This is followed by detailed measurements on particular dilutions which demonstrate spin glass behavior. Pure TbNi{sub 2}Ge{sub 2} is an Ising antiferromagnet with a several distinct metamagnetic states below 17 K. As the terbium is alloyed with yttrium, these magnetic states are weakened in a consistent manner, as is seen in measurements of the transition temperatures and analysis of Curie-Weiss behavior at high temperature. At low concentrations of terbium, below 35%, long range order is no longer present and a spin-glass-like state emerges. This state is studied through various measurements, dc and ac susceptibility, resistivity, and specific heat. This magnetic behavior was then compared to that of other well characterized spin glasses. It is concluded that there is a region of concentration s for which a spin

  9. Characterization of the Dilute Ising Antiferromagnet

    Energy Technology Data Exchange (ETDEWEB)

    Wiener, Timothy [Iowa State Univ., Ames, IA (United States)

    2000-09-12

    A spin glass is a magnetic ground state in which ferromagnetic and antiferromagnetic exchange interactions compete, thereby creating frustration and a multidegenerate state with no long range order. An Ising system is a system where the spins are constrained to lie parallel or antiparallel to a primary axis. There has been much theoretical interest in the past ten years in the effects of applying a magnetic field transverse to the primary axis in an Ising spin glass at low temperatures and thus study phase transitions at the T=0 limit. The focus of this study is to search for and characterize a new Ising spin glass system. This is accomplished by site diluting yttrium for terbium in the crystalline material TbNi2Ge2. The first part of this work gives a brief overview of the physics of rare earth magnetism and an overview of experimental characteristics of spin glasses. This is followed by the methodology used to manufacture the large single crystals used in this study, as well as the measurement techniques used. Next, a summary of the results of magnetic measurements on across the dilution series from pure terbium to pure yttrium is presented. This is followed by detailed measurements on particular dilutions which demonstrate spin glass behavior. Pure TbNi2Ge2 is an Ising antiferromagnet with a several distinct metamagnetic states below 17 K. As the terbium is alloyed with yttrium, these magnetic states are weakened in a consistent manner, as is seen in measurements of the transition temperatures and analysis of Curie-Weiss behavior at high temperature. At low concentrations of terbium, below 35%, long range order is no longer present and a spin-glass-like state emerges. This state is studied through various measurements, dc and ac susceptibility, resistivity, and specific heat. This magnetic behavior was then compared to that of other well characterized spin glasses. It is concluded that there is a region of

  10. Exclusion of Nitrate from Frozen Aqueous Solutions

    Science.gov (United States)

    Marrocco, H. A.; Michelsen, R. R.

    2013-12-01

    Reactions occurring at the surface of ice, sea ice, and snow in Earth's cryosphere have an impact on the composition of the overlying atmosphere. In order to elucidate reaction mechanisms and model their contributions to atmospheric processes, the morphology of frozen aqueous surfaces and amounts of reactants contained therein must be determined. To this end, the exclusion of nitrate ions to the surface of frozen aqueous solutions has been studied by attenuated total reflection infrared spectroscopy (ATR-IR). In this technique the near-surface region of the frozen films are interrogated to a depth of a few hundred nanometers from the film-crystal interface. Aqueous solutions (0.001 to 0.01 M) of sodium nitrate (NaNO3), magnesium nitrate (Mg(NO3)2), and nitric acid (HNO3) were quickly frozen on the germanium ATR crystal and observed at a constant temperature of about -18°C. In addition to ice and the solutes, liquid water in varying amounts was observed in the spectra. The amount of nitrate in the surface liquid is three to four orders of magnitude higher than in the unfrozen solution. While all the nitrate salts exhibit exclusion to the unfrozen surface, the dynamics are different for different counter-ions. Results are compared to freezing point depression data and the predictions of equilibrium thermodynamics.

  11. The precipitation of potassium aluminium sulphate from aqueous solution

    Science.gov (United States)

    Mullin, J. W.; Žáček, S.

    1981-06-01

    A precipitation study has been made with potassium aluminium sulphate (potash alum) produced by mixing aqueous solutions of its constituent salts. Rates of nucleation, as indicated by the induction period, were measured for both agitated and non-agitated solutions over the temperature range 15-35°C. Nucleation rates increase with increases in agitation, temperature and supersaturation, but the latter has the dominant effect, as predicted by classical nucleation theory. The temperature-dependence of the interfacial tension is evaluated.

  12. Salt treatment Fukushima

    Energy Technology Data Exchange (ETDEWEB)

    Schaefer, Stefan [NUKEM Technologies GmbH, Alzenau (Germany)

    2013-07-01

    The Task of NUKEM Technologies GmbH is to develop a technical solution for the treatment of salt containing effluents at Fukushima Daiichi. The target of the treatment is a solidified product suitable for the safe storage on site. Therefore, NUKEM investigated several technologies (direct cementation, drying and storage, drying and subsequent cementation) in order to find a fit for purpose solution. The following tasks have been considered: (a) Mechanical strength and homogeneity of the product; (b) Cost efficient solution (cost for the drying system vs. reduced amount of storage containers); (c) Proven technology; (d) On site storage. NUKEM made some practical test in parallel with different recipes. The aim was to embed as much as possible salt quantity into the cement matrix, but still meet the requested mechanical strength and required homogeneity. As a result NUKEM recommended to apply the following technologies (a) a drying system, to produce a dry salt product (b) a cementation facility, to generate a homogeneous salt/cement matrix (c) a filling station with attached CMS (Container measuring station) to fill the resulting cement/salt matrix into containers suitable for the storage at Fukushima Daiichi. (orig.)

  13. Stable isotope dilution assays in mycotoxin analysis

    Energy Technology Data Exchange (ETDEWEB)

    Rychlik, Michael; Asam, Stefan [Universitaet Muenchen, Lehrstuhl fuer Lebensmittelchemie der Technischen, Garching (Germany)

    2008-01-15

    The principle and applications of stable isotope dilution assays (SIDAs) in mycotoxin analysis are critically reviewed. The general section includes historical aspects of SIDAs, the prerequisites and limitations of the use of stable isotopically labelled internal standards, and possible calibration procedures. In the application section actual SIDAs for the analysis of trichothecenes, zearalenone, fumonisins, patulin, and ochratoxin A are presented. The syntheses and availability of labelled mycotoxins for use as internal standards is reviewed and specific advances in food analysis and toxicology are demonstrated. The review indicates that LC-MS applications, in particular, require the use of stable isotopically labelled standards to compensate for losses during clean-up and for discrimination due to ion suppression. As the commercial availability of these compounds continues to increase, SIDAs can be expected to find expanding use in mycotoxin analysis. (orig.)

  14. Guideline on Isotope Dilution Mass Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Gaffney, Amy [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2017-05-19

    Isotope dilution mass spectrometry is used to determine the concentration of an element of interest in a bulk sample. It is a destructive analysis technique that is applicable to a wide range of analytes and bulk sample types. With this method, a known amount of a rare isotope, or ‘spike’, of the element of interest is added to a known amount of sample. The element of interest is chemically purified from the bulk sample, the isotope ratio of the spiked sample is measured by mass spectrometry, and the concentration of the element of interest is calculated from this result. This method is widely used, although a mass spectrometer required for this analysis may be fairly expensive.

  15. Diluted magnetic semiconductors with narrow band gaps

    Science.gov (United States)

    Gu, Bo; Maekawa, Sadamichi

    2016-10-01

    We propose a method to realize diluted magnetic semiconductors (DMSs) with p - and n -type carriers by choosing host semiconductors with a narrow band gap. By employing a combination of the density function theory and quantum Monte Carlo simulation, we demonstrate such semiconductors using Mn-doped BaZn2As2 , which has a band gap of 0.2 eV. In addition, we found a nontoxic DMS Mn-doped BaZn2Sb2 , of which the Curie temperature Tc is predicted to be higher than that of Mn-doped BaZn2As2 , the Tc of which was up to 230 K in a recent experiment.

  16. Physics of Spin Casting Dilute Solutions

    CERN Document Server

    Karpitschka, Stefan; Riegler, Hans

    2012-01-01

    We analyze the spin casting of dilute (ideal) binary mixtures of non-volatile solutes in volatile solvents as a prototype for evaporation-controlled processes that are increasingly used to deposit specifically structured (sub)monolayers ("evaporation-induced self-assembly"). The first analytical description of the thinning of a volatile liquid film simultaneously subject to spinning and evaporation is presented. It shows, that the duration of a spin casting process is linked to the process parameters via power laws. A diffusion-advection model leads analytically to the equation governing the spatio-temporal evolution of the internal film composition. Its solution reveals that the solute concentration enrichment, its gradient, and its time evolution are related to the process parameters via power laws. The physics behind the power laws is uncovered and discussed. This reveales universal insights into the interplay between the control parameters and their impact on the spatiotemporal evolution of the film compo...

  17. Fermi Surface of the Most Dilute Superconductor

    Science.gov (United States)

    Lin, Xiao; Zhu, Zengwei; Fauqué, Benoît; Behnia, Kamran

    2013-04-01

    The origin of superconductivity in bulk SrTiO3 is a mystery since the nonmonotonous variation of the critical transition with carrier concentration defies the expectations of the crudest version of the BCS theory. Here, employing the Nernst effect, an extremely sensitive probe of tiny bulk Fermi surfaces, we show that, down to concentrations as low as 5.5×1017cm-3, the system has both a sharp Fermi surface and a superconducting ground state. The most dilute superconductor currently known therefore has a metallic normal state with a Fermi energy as little as 1.1 meV on top of a band gap as large as 3 eV. The occurrence of a superconducting instability in an extremely small, single-component, and barely anisotropic Fermi surface implies strong constraints for the identification of the pairing mechanism.

  18. Ultrafast magnetization dynamics in diluted magnetic semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Morandi, O [INRIA Nancy Grand-Est and Institut de Recherche en Mathematiques Avancees, 7 rue Rene Descartes, F-67084 Strasbourg (France); Hervieux, P-A; Manfredi, G [Institut de Physique et Chimie des Materiaux de Strasbourg, 23 rue du Loess, F-67037 Strasbourg (France)], E-mail: morandi@dipmat.univpm.it

    2009-07-15

    We present a dynamical model that successfully explains the observed time evolution of the magnetization in diluted magnetic semiconductor quantum wells after weak laser excitation. Based on the pseudo-fermion formalism and a second-order many-particle expansion of the exact p-d exchange interaction, our approach goes beyond the usual mean-field approximation. It includes both the sub-picosecond demagnetization dynamics and the slower relaxation processes that restore the initial ferromagnetic order in a nanosecond timescale. In agreement with experimental results, our numerical simulations show that, depending on the value of the initial lattice temperature, a subsequent enhancement of the total magnetization may be observed within the timescale of a few hundred picoseconds.

  19. Tunnel backfill erosion by dilute water

    Energy Technology Data Exchange (ETDEWEB)

    Olin, M. [VTT Technical Research Centre of Finland, Espoo (Finland)

    2014-03-15

    The goal was to estimate smectite release from tunnel backfill due to dilute groundwater pulse during post glacial conditions. The plan was to apply VTT's two different implementations (BESW{sub D} and BESW{sub S}) of well-known model of Neretnieks et al. (2009). It appeared difficult to produce repeatable results using this model in COMSOL 4.2 environment, therefore a semi-analytical approximate approach was applied, which enabled to take into account both different geometry and smectite content in tunnel backfill as compared to buffer case. The results are quite similar to buffer results due to the decreasing effect of smaller smectite content and the increasing effect of larger radius. (orig.)

  20. Stable isotope dilution assays in mycotoxin analysis.

    Science.gov (United States)

    Rychlik, Michael; Asam, Stefan

    2008-01-01

    The principle and applications of stable isotope dilution assays (SIDAs) in mycotoxin analysis are critically reviewed. The general section includes historical aspects of SIDAs, the prerequisites and limitations of the use of stable isotopically labelled internal standards, and possible calibration procedures. In the application section actual SIDAs for the analysis of trichothecenes, zearalenone, fumonisins, patulin, and ochratoxin A are presented. The syntheses and availability of labelled mycotoxins for use as internal standards is reviewed and specific advances in food analysis and toxicology are demonstrated. The review indicates that LC-MS applications, in particular, require the use of stable isotopically labelled standards to compensate for losses during clean-up and for discrimination due to ion suppression. As the commercial availability of these compounds continues to increase, SIDAs can be expected to find expanding use in mycotoxin analysis.

  1. Critical exponents for diluted resistor networks.

    Science.gov (United States)

    Stenull, O; Janssen, H K; Oerding, K

    1999-05-01

    An approach by Stephen [Phys. Rev. B 17, 4444 (1978)] is used to investigate the critical properties of randomly diluted resistor networks near the percolation threshold by means of renormalized field theory. We reformulate an existing field theory by Harris and Lubensky [Phys. Rev. B 35, 6964 (1987)]. By a decomposition of the principal Feynman diagrams, we obtain diagrams which again can be interpreted as resistor networks. This interpretation provides for an alternative way of evaluating the Feynman diagrams for random resistor networks. We calculate the resistance crossover exponent phi up to second order in epsilon=6-d, where d is the spatial dimension. Our result phi=1+epsilon/42+4epsilon(2)/3087 verifies a previous calculation by Lubensky and Wang, which itself was based on the Potts-model formulation of the random resistor network.

  2. Optical processes in dilute nitrides Semiconductors; Alloys

    CERN Document Server

    Potter, R J

    2003-01-01

    This thesis is concerned with the narrow bandgap semiconductor alloys known as dilute nitrides. The initial part of this project was concerned with characterisation of chemical beam epitaxy (CBE) grown samples so that growth techniques could be refined. Early samples show evidence of structural/compositional disorder resulting from the large miscibility gap induced by nitrogen. Non-equilibrium growth was employed to overcome this, eventually resulting in improved material. In the second part of this project, steady-state and time-resolved photoluminescence, along with photomodulated reflectance were employed to investigate the optical properties of molecular beam epitaxy (MBE) grown GalnNAs, GaNAs and InGaAs quantum wells (QWs). Low temperature results show evidence of carrier localization, which was interpreted in terms of structural/compositional fluctuations induced by the nitrogen incorporation. Poor photoluminescence efficiency and rapid decay of emission kinetics indicate the presence of strong non-radi...

  3. Dilute Oxygen Combustion Phase 3 Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Riley, M.F.; Ryan, H.M.

    2000-05-31

    Dilute Oxygen Combustion (DOC) burners have been successfully installed and operated in the reheat furnace at Auburn Steel Co., Inc., Auburn, NY, under Phase 3 of the Dilute Oxygen Combustion project. Two new preheat zones were created employing a total of eight 6.5 MMBtu/hr capacity burners. The preheat zones provide a 30 percent increase in maximum furnace production rate, from 75 tph to 100 tph. The fuel rate is essentially unchanged, with the fuel savings expected from oxy-fuel combustion being offset by higher flue gas temperatures. When allowance is made for the high nitrogen level and high gas phase temperature in the furnace, measured NOx emissions are in line with laboratory data on DOC burners developed in Phase 1 of the project. Burner performance has been good and there have been no operating or maintenance problems. The DOC system continues to be used as part of Auburn Steel?s standard reheat furnace practice. High gas phase temperature is a result of the high firing density needed to achieve high production rates, and little opportunity exists for improvement in that area. However, fuel and NOx performance can be improved by further conversion of furnace zones to DOC burners, which will lower furnace nitrogen levels. Major obstacles are cost and concern about increased formation of oxide scale on the steel. Oxide scale formation may be enhanced by exposure of the steel to higher concentrations of oxidizing gas components (primarily products of combustion) in the higher temperature zones of the furnace. Phase 4 of the DOC project will examine the rate of oxide scale formation in these higher temperature zones and develop countermeasures that will allow DOC burners to be used successfully in these furnace zones.

  4. Dilute Oxygen Combustion - Phase 3 Report

    Energy Technology Data Exchange (ETDEWEB)

    Riley, Michael F.

    2000-05-31

    Dilute Oxygen Combustion (DOC) burners have been successfully installed and operated in the reheat furnace at Auburn Steel Co., Inc., Auburn, NY, under Phase 3 of the Dilute Oxygen Combustion project. Two new preheat zones were created employing a total of eight 6.5 MMBtu/hr capacity burners. The preheat zones provide a 30 percent increase in maximum furnace production rate, from 75 tph to 100 tph. The fuel rate is essentially unchanged, with the fuel savings expected from oxy-fuel combustion being offset by higher flue gas temperatures. When allowance is made for the high nitrogen level and high gas phase temperature in the furnace, measured NOx emissions are in line with laboratory data on DOC burners developed in Phase 1 of the project. Burner performance has been good, and there have been no operating or maintenance problems. The DOC system continues to be used as part of Auburn Steel's standard reheat furnace practice. High gas phase temperature is a result of the high firing density needed to achieve high production rates, and little opportunity exists for improvement in that area. However, fuel and NOx performance can be improved by further conversion on furnace zones to DOC burners, which will lower furnace nitrogen levels. Major obstacles are cost and concern about increased formation of oxide scale on the steel. Oxide scale formation may be enhanced by exposure of the steel to higher concentrations of oxidizing gas components (primarily products of combustion) in the higher temperature zones of the furnace. Phase 4 of the DOC project will examine the rate of oxide scale formation in these higher temperature zones and develop countermeasures that will allow DOC burners to be used successfully in these furnace zones.

  5. A method for separating water soluble organics from a process stream by aqueous biphasic extraction

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, David J.; Mego, William A.

    1997-12-01

    The present invention relates to a method for separating water-miscible organic species from a process stream by aqueous biphasic extraction. In particular, the method includes extracting the organic species into a polymer-rich phase of an aqueous biphase system in which the process stream comprises the salt-rich phase, and, next, separating the polymer from the extracted organic species by contacting the loaded, polymer-rich phase with a water-immiscible organic phase. Alternatively, the polymer can be separated from the extracted organic species by raising the temperature of the loaded, polymer-rich phase above the cloud point, such that the polymer and the water-soluble organic species separate into two distinct aqueous phases. In either case, a substantially salt-free, concentrated aqueous solution containing the organic species is recovered.

  6. Laser-induced photoelectrochemistry: scavenging of photoemitted electrons in aqueous and non-aqueous solutions by electroactive organic species

    Energy Technology Data Exchange (ETDEWEB)

    Richardson, J.H. (Lawrence Livermore Lab., CA); Kovalenko, L.J.; Deutscher, S.B.; Harrar, J.E.; Perone, S.P.

    1980-01-01

    Photoemission current at a mercury electrode has been characterized electrochemically for aqueous solutions of methyl viologen, the disodium salt of anthraquinone-1,5-disulfonic acid, hydroquinone, p-benzoquinone, and chlorophyllin, and in DMF solutions of N/sub 2/O and anthraquinone. The scavenging species could be determined by comparing photoemission current-voltage curves with polarographic and cyclic voltammetric data. 11 figures.

  7. The evaporation behavior of sessile droplets from aqueous saline solutions.

    Science.gov (United States)

    Soulié, Virginie; Karpitschka, Stefan; Lequien, Florence; Prené, Philippe; Zemb, Thomas; Moehwald, Helmuth; Riegler, Hans

    2015-09-14

    Quantitative experiments on the evaporation from sessile droplets of aqueous saline (NaCl) solutions show a strong dependence on salt concentration and droplet shape. The experiments were performed with seven decades of initial NaCl concentrations, with various droplet sizes and with different contact angles. The evaporation rate is significantly lower for high salt concentrations and small contact angles than what is expected from the well-accepted diffusion-controlled evaporation scenario for sessile droplets, even if the change of the vapor pressure due to the salt is taken into account. Particle tracking velocimetry reveals that this modification of the evaporation behavior is caused by marangoni flows that are induced by surface tension gradients originating from the local evaporative peripheral salt enrichment. In addition it is found that already very low salt concentrations lead to a pinning of the three phase contact line. Whereas droplets with concentration ≥10(-6) M NaCl are pinned as soon as evaporation starts, droplets with lower salt concentration do evaporate in a constant contact angle mode. Aside from new, fundamental insights the findings are also relevant for a better understanding of the widespread phenomenon of corrosion initiated by sessile droplets.

  8. Effect of electrolyte on the microstructure and yielding of aqueous dispersions of colloidal clay

    OpenAIRE

    Ali, Samim; Bandyopadhyay, Ranjini

    2015-01-01

    Na-montmorillonite is a natural clay mineral and is available in abundance in nature. The aqueous dispersions of charged and anisotropic platelets of this mineral exhibit non-ergodic kinetically arrested states ranging from soft glassy phases dominated by interparticle repulsions to colloidal gels stabilized by salt induced attractive interactions. When the salt concentration in the dispersing medium is varied systematically, viscoelasticity and yield stress of the dispersion show non-monoton...

  9. Mechanism for salt scaling

    Science.gov (United States)

    Valenza, John J., II

    Salt scaling is superficial damage caused by freezing a saline solution on the surface of a cementitious body. The damage consists of the removal of small chips or flakes of binder. The discovery of this phenomenon in the early 1950's prompted hundreds of experimental studies, which clearly elucidated the characteristics of this damage. In particular it was shown that a pessimum salt concentration exists, where a moderate salt concentration (˜3%) results in the most damage. Despite the numerous studies, the mechanism responsible for salt scaling has not been identified. In this work it is shown that salt scaling is a result of the large thermal expansion mismatch between ice and the cementitious body, and that the mechanism responsible for damage is analogous to glue-spalling. When ice forms on a cementitious body a bi-material composite is formed. The thermal expansion coefficient of the ice is ˜5 times that of the underlying body, so when the temperature of the composite is lowered below the melting point, the ice goes into tension. Once this stress exceeds the strength of the ice, cracks initiate in the ice and propagate into the surface of the cementitious body, removing a flake of material. The glue-spall mechanism accounts for all of the characteristics of salt scaling. In particular, a theoretical analysis is presented which shows that the pessimum concentration is a consequence of the effect of brine pockets on the mechanical properties of ice, and that the damage morphology is accounted for by fracture mechanics. Finally, empirical evidence is presented that proves that the glue-small mechanism is the primary cause of salt scaling. The primary experimental tool used in this study is a novel warping experiment, where a pool of liquid is formed on top of a thin (˜3 mm) plate of cement paste. Stresses in the plate, including thermal expansion mismatch, result in warping of the plate, which is easily detected. This technique revealed the existence of

  10. Synthesis and Self-Assembly of Triangulenium Salts

    DEFF Research Database (Denmark)

    Shi, Dong

    This thesis describes the design and synthesis of asymmetrically substituted amphiphilic tis(dialkylamino)trioxiatriangulenium (ATOTA+) salts with different counter ions. Attention was focused on exploring the assembling properties of the ATOTA+ salts in aqueous media. A direct vortexing-processe......This thesis describes the design and synthesis of asymmetrically substituted amphiphilic tis(dialkylamino)trioxiatriangulenium (ATOTA+) salts with different counter ions. Attention was focused on exploring the assembling properties of the ATOTA+ salts in aqueous media. A direct vortexing......, highly ordered, and free-floating bilayer nanosheets through prolonged vigorous shaking. In this study, a mechanism for the self-assembly process agitated by prolonged vigorous shaking is proposed. It is proposed that the self-assembly is realized via a intermediated monolayer formed at the dynamic air......–water interfaces and lateral compression of the monolayer results in the collapsing toward the formation of bilayer nanosheets. The nanosheets showed excellent stability after standing over 10 months stocked in a close vial at ambient conditions due to the ionic atmosphere surrounding its charged surfaces...

  11. Toxicity of contaminated sediments in dilution series with control sediments

    Science.gov (United States)

    Nelson, M.K.; Landrum, P.F.; Burton, G.A.; Klaine, S.J.; Crecelius, E.A.; Byl, T.D.; Gossiaux, Duane C.; Tsymbal, V.N.; Cleveland, L.; Ingersoll, Christopher G.; Sasson-Brickson, G.

    1993-01-01

    The use of dilutions has been the foundation of our approach for assessing contaminated water, and accordingly, it may be important to establish similar or parallel approaches for sediment dilutions. Test organism responses to dilution gradients can identify the degree of necessary sediment alteration to reduce the toxicity. Using whole sediment dilutions to represent the complex interactions of in situ sediments can identify the toxicity, but the selection of the appropriate diluent for the contaminated sediment may affect the results and conclusions drawn. Contaminated whole sediments were examined to evaluate the toxicity of dilutions of sediments with a diversity of test organisms. Dilutions of the contaminated sediments were prepared with differing diluents that varied in organic carbon content, particle size distribution, and volatile solids. Studies were conducted using four macroinvertebrates and a vascular, rooted plant. Responses by some test organisms followed a sigmoidal dose-response curve, but others followed a U-shaped curve. Initial dilutions reduced toxicity as expected, but further dilution resulted in an increase in toxicity. The type of diluent used was an important factor in assessing the sediment toxicity, because the control soil reduced toxicity more effectively than sand as a diluent of the same sediment. Using sediment chemical and physical characteristics as an indicator of sediment dilution may not be as useful as chemical analysis of contaminants, but warrants further investigation.

  12. Dilution in a Dense Bottom Jet in Cross Currents

    DEFF Research Database (Denmark)

    Petersen, O.; Larsen, Torben

    1998-01-01

    A 3-dimensional numerical model describing the dilution in the near field around dense vertical jets in a cross flow is formulated and validated against laboratory experiments. The validation shows that the model reproduces the flow pattern well, though the dilution is underestimated by 20%. The ......%. The model is applied to a case study where the dilution from two vertical jets at an angle in shallow water is described. It is demonstrated that a 20% increase in dilution is possible. It is concluded that the model may become a valuable tool in diffusor design....

  13. 21 CFR 866.2500 - Microtiter diluting and dispensing device.

    Science.gov (United States)

    2010-04-01

    ... SERVICES (CONTINUED) MEDICAL DEVICES IMMUNOLOGY AND MICROBIOLOGY DEVICES Microbiology Devices § 866.2500... a mechanical device intended for medical purposes to dispense or serially dilute very...

  14. Analyses of beyond design basis accident homogeneous boron dilution scenarios

    Energy Technology Data Exchange (ETDEWEB)

    Kereszturi, Andras; Hegyi, Gyoergy; Maraczy, Csaba; Trosztel, Istvan; Tota, Adam [Hungarian Academy of Sciences, Centre for Energy Research, Budapest (Hungary); Karsa, Zoltan [NUBIKI Nuclear Safety Research Institute, Ltd., Budapest (Hungary)

    2015-09-15

    Homogeneous boron dilution scenarios in a VVER-440 reactor were analyzed using the coupled KIKO3D-ATHLET code. The scenarios are named ''homogeneous'' because of the very slow dilution caused by a rupture in the heat exchanger of the makeup system. Without the presented analyses, a significant contribution of the homogeneous boron dilution to the Core Damage Frequency (CDF) had to be assumed in the Probabilistic Safety Analyses (PSA). According to the combined results of the presented deterministic and probabilistic analyses, the final conclusion is that boron dilution transients don't give significant contribution to the CDF for the investigated VVER-440 NPP.

  15. Dilution in a Dense Bottom Jet in Cross Currents

    DEFF Research Database (Denmark)

    Petersen, O.; Larsen, Torben

    1998-01-01

    A 3-dimensional numerical model describing the dilution in the near field around dense vertical jets in a cross flow is formulated and validated against laboratory experiments. The validation shows that the model reproduces the flow pattern well, though the dilution is underestimated by 20......%. The model is applied to a case study where the dilution from two vertical jets at an angle in shallow water is described. It is demonstrated that a 20% increase in dilution is possible. It is concluded that the model may become a valuable tool in diffusor design....

  16. Overlap amplitude and localization properties in aperiodic diluted and non-diluted direct electric transmission lines

    Science.gov (United States)

    Lazo, E.; Castro, C. E.; Cortés-Cortés, F.

    2016-09-01

    In this work we study the relationship existing between the localization properties of the diluted and non-diluted direct electrical transmission lines with the overlap amplitude Cijω = 2 | Iiω Ijω | , where Ijω is the amplitude of the electric current function at jth cell of the transmission line for the state with frequency ω. We distribute two values of inductances LA and LB, according to the generalized aperiodic Thue-Morse m-tupling sequence. We find that the behavior of Ci,jω is directly related to the localization properties of the aperiodic sequences measured by the ξ normalized participation number, the Rq Rényi entropies and the μq moments. In addition, we generalize the scaling relationship for the overlap amplitude Ci,jω, i.e., =(2/N) 2 q.

  17. Effect of inorganic salts on crystallization of poly(ethylene glycol) in frozen solutions.

    Science.gov (United States)

    Izutsu, Ken-ichi; Aoyagi, Nobuo

    2005-01-06

    The effect of inorganic salts on eutectic crystallization of poly(ethylene glycol) (PEG) 1500-20,000 in frozen solution was studied to model the polymer and inorganic salt interaction in freeze-dried formulations. Thermal analysis of an aqueous PEG 3000 solution showed a eutectic PEG crystallization exotherm at approximately -47 degrees C and a subsequent PEG crystal melting endotherm at -14.9 degrees C. Addition of sodium chloride prevented the PEG crystallization in the freeze-concentrated solution surrounding ice crystals. Higher concentration NaCl was required to retain higher molecular weight PEG in the amorphous state. Various inorganic salts prevented the PEG crystallization to varying degrees depending mainly on the position of the anion in the Hofmeister's lyotropic series. Some salting-in and 'intermediate' salts (NaSCN, NaI, NaBr, NaCl, LiCl, KCl, and RbCl) inhibited the crystallization of PEG 7500 in frozen solutions. On the other hand, salting-out salts (NaH2PO4, Na2HPO4, Na2SO4, and NaF) did not show an apparent effect on the PEG crystallization. Some salting-out salts induced PEG crystallization in PEG and sucrose combination frozen solutions. The varying abilities of salts to prevent the PEG crystallization in frozen solutions strongly suggested that the solutes had different degrees of miscibility in the freeze-concentrates.

  18. VISCOSITY BEHAVIOR OF PS/TOLUENE SOLUTION IN DILUTE AND EXTREMELY DILUTE CONCENTRATION REGION

    Institute of Scientific and Technical Information of China (English)

    DU Dengxue; ZUO Ju; CHEN Yu; NING Hui

    2003-01-01

    The influences of both the volume of PS/toluene solution in the Ubbelohde viscometer and the precision of the time measuring on the viscosity behavior in dilute and extremely diluteconcentration region are investigated It was found that the influence of the former can neglect, but that of the latter is so prominent that the data fluctuate bitterly and linearity of the curve of the reduced viscosity vs. Concentration (ηsp/c~c) becomes too bad to obey the Huggins equation down to the extremely dilute region, despite the error of the flow times △t ≤ 0.2s, which is permitted by the conventional method of viscosity measurement. Through strict mathematical analyses, it was found that thc error (E) of the reduced viscosity is in proportion and inverse proportion to △t and concentration c, respectively. So the less the concentration, the more the error is. Consequently, a lowest concentration limit cL corresponding to given experimental error may exist and it will be meaningless for further operation below cL because of the great fluctuation of the data. Therefore, itneeds to seriously reconsider the application of the conventional method of Ubbelohde viscosity measurement in the extremely dilute polymer solution under traditional conditions because of the great influence of the experimental error.

  19. Catalyst used in 1,2-epoxyalkane preparation is obtained by heating tetraalkyl ammonium salts, tetraalkyl siloxanes and amines, calcining and treating with a tetraalkoxy compound

    DEFF Research Database (Denmark)

    2001-01-01

    NOVELTY - The catalyst, used in 1,2-epoxyalkane preparation, is obtained by heat treating an aqueous composition comprising tetraalkyl ammonium salts, tetraalkyl siloxanes and amines, removing the template by calcining and treating with a tetraalkoxy compound......NOVELTY - The catalyst, used in 1,2-epoxyalkane preparation, is obtained by heat treating an aqueous composition comprising tetraalkyl ammonium salts, tetraalkyl siloxanes and amines, removing the template by calcining and treating with a tetraalkoxy compound...

  20. Dilute Surfactant Methods for Carbonate Formations

    Energy Technology Data Exchange (ETDEWEB)

    Kishore K. Mohanty

    2006-02-01

    There are many fractured carbonate reservoirs in US (and the world) with light oil. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). The process of using dilute anionic surfactants in alkaline solutions has been investigated in this work for oil recovery from fractured oil-wet carbonate reservoirs both experimentally and numerically. This process is a surfactant-aided gravity drainage where surfactant diffuses into the matrix, lowers IFT and contact angle, which decrease capillary pressure and increase oil relative permeability enabling gravity to drain the oil up. Anionic surfactants have been identified which at dilute concentration of 0.05 wt% and optimal salinity can lower the interfacial tension and change the wettability of the calcite surface to intermediate/water-wet condition as well or better than the cationic surfactant DTAB with a West Texas crude oil. The force of adhesion in AFM of oil-wet regions changes after anionic surfactant treatment to values similar to those of water-wet regions. The AFM topography images showed that the oil-wetting material was removed from the surface by the anionic surfactant treatment. Adsorption studies indicate that the extent of adsorption for anionic surfactants on calcite minerals decreases with increase in pH and with decrease in salinity. Surfactant adsorption can be minimized in the presence of Na{sub 2}CO{sub 3}. Laboratory-scale surfactant brine imbibition experiments give high oil recovery (20-42% OOIP in 50 days; up to 60% in 200 days) for initially oil-wet cores through wettability alteration and IFT reduction. Small (<10%) initial gas saturation does not affect significantly the rate of oil recovery in the imbibition process, but larger gas saturation decreases the oil recovery rate. As the core permeability decreases, the rate of oil recovery reduces

  1. Aqueous Solutions of Ionic Liquids: Microscopic Assembly.

    Science.gov (United States)

    Vicent-Luna, Jose Manuel; Dubbeldam, David; Gómez-Álvarez, Paula; Calero, Sofia

    2016-02-01

    Aqueous solutions of ionic liquids are of special interest, due to the distinctive properties of ionic liquids, in particular, their amphiphilic character. A better understanding of the structure-property relationships of such systems is hence desirable. One of the crucial molecular-level interactions that influences the macroscopic behavior is hydrogen bonding. In this work, we conduct molecular dynamics simulations to investigate the effects of ionic liquids on the hydrogen-bond network of water in dilute aqueous solutions of ionic liquids with various combinations of cations and anions. Calculations are performed for imidazolium-based cations with alkyl chains of different lengths and for a variety of anions, namely, [Br](-), [NO3](-), [SCN](-) [BF4](-), [PF6](-), and [Tf2N](-). The structure of water and the water-ionic liquid interactions involved in the formation of a heterogeneous network are analyzed by using radial distribution functions and hydrogen-bond statistics. To this end, we employ the geometric criterion of the hydrogen-bond definition and it is shown that the structure of water is sensitive to the amount of ionic liquid and to the anion type. In particular, [SCN](-) and [Tf2N](-) were found to be the most hydrophilic and hydrophobic anions, respectively. Conversely, the cation chain length did not influence the results.

  2. Photoluminescence of urine salts

    Science.gov (United States)

    Bordun, O.; Drobchak, O.

    2008-02-01

    Photoexcitation and luminescence spectra of dried urine sample under laser excitation were studied. Luminescence spectra of urine are determined by luminescence of urea which is the main component of urine. The presence of pathological salts in urine leads to the long-wave shifting of maxima of luminescence and to the decreasing of luminescence intensity.

  3. Learning SaltStack

    CERN Document Server

    Myers, Colton

    2015-01-01

    If you are a system administrator who manages multiple servers, then you know how difficult it is to keep your infrastructure in line. If you've been searching for an easier way, this book is for you. No prior experience with SaltStack is required.

  4. What Are Bath Salts?

    Science.gov (United States)

    ... in Missouri. She won the 3rd place 2013 Addiction Science Award . Read More » 0 Comments Bath Salts: An Emerging Danger February 05, 2013 / Sara Bellum ... copy Listen Drug Facts ... Nicotine, & E-Cigarettes Brain and Addiction Drug Overdoses in Youth HIV/AIDS and Drug ...

  5. Carpinteria Salt Marsh Habitat Polygons

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — We identified five common habitat types in Carpinteria Salt Marsh: channels, pans (flats), marsh, salt flat and upland. We then drew polygons around each habitat...

  6. Dilution jet experiments in compact combustor configurations

    Science.gov (United States)

    Greber, I.; Zizelman, J.

    1984-01-01

    This project concerns the effects of cooling jets on the velocity and temperature fields in a compact reverse flow combustor. The work is motivated by the need to limit the temperatures of post combustion gases in jet engines to values within the endurance capabilities of turbine blades. The application requires not only that the temperature be kept sufficiently low but also that a suitably tailored temperature profile be provided at the combustor exit, with higher temperatures generally permissible at the blade tip than at the blade root because of higher centrifugal loads at the root. Flows in reverse flow combustor accelerate both longitudinally because of area changes and transversely because of flow turning. The current project started with flow visualization experiments in water, using aqueous solutions of zinc bromide to model the relatively higher density of cooling jets.

  7. Salt ingestion caves.

    Directory of Open Access Journals (Sweden)

    Lundquist Charles A.

    2006-01-01

    Full Text Available Large vertebrate herbivores, when they find a salt-bearing layer of rock, say in a cliff face, can produce sizable voids where, overgenerations, they have removed and consumed salty rock. The cavities formed by this natural animal process constitute a uniqueclass of caves that can be called salt ingestion caves. Several examples of such caves are described in various publications. Anexample in Mississippi U.S.A., Rock House Cave, was visited by the authors in 2000. It seems to have been formed by deer orbison. Perhaps the most spectacular example is Kitum Cave in Kenya. This cave has been excavated to a length over 100 metersby elephants. An ancient example is La Cueva del Milodon in Chile, which is reported to have been excavated by the now extinctmilodon, a giant ground sloth. Still other possible examples can be cited. This class of caves deserves a careful definition. First, thecavity in rock should meet the size and other conventions of the locally accepted definition of a cave. Of course this requirement differsin detail from country to country, particularly in the matter of size. The intent is to respect the local conventions. The characteristicthat human entry is possible is judged to be a crucial property of any recognized cave definition. Second, the cavity should besignificantly the result of vertebrate animal consumption of salt-bearing rock. The defining process is that rock removed to form thecave is carried away in the digestive track of an animal. While sodium salts are expected to be the norm, other salts for which thereis animal hunger are acceptable. Also some other speleogenesis process, such as solution, should not be excluded as long as it issecondary in formation of a cave in question.

  8. Salt fluoridation and oral health

    OpenAIRE

    Thomas M. Marthaler

    2013-01-01

    The aim of this paper is to make known the potential of fluoridated salt in community oral health programs, particularly in South Eastern Europe. Since 1922, the addition of iodine to salt has been successful in Switzerland. Goiter is virtually extinct. By 1945, the cariesprotective effect of fluorides was well established. Based on the success of water fluoridation, a gynecologist started adding of fluoride to salt. The sale of fluoridated salt began in 1956 in the Swiss Canton of Zurich,...

  9. Treatment of Aqueous Solutions

    NARCIS (Netherlands)

    Van Spronsen, J.; Witkamp, G.J.

    2013-01-01

    The invention is directed to a process for the recovery or removal of one or more crystallizable compounds from an aqueous solution containing, apart from the said crystallizable compounds, one or more organic or inorganic scale- forming or scale-inducing materials having a lower solubility in water

  10. Performance of the TCDQ diluter system

    CERN Document Server

    Presland, A

    2005-01-01

    A single sided mobile graphite diluter block TCDQ, in combination with a two-sided secondary collimator TCS and an iron shield TCDQM, will be installed in front of the superconducting quadrupole Q4 magnets in IR6, in order to protect it and other downstream LHC machine elements from destruction in the event of a beam dump that is not synchronised with the abort gap. The TCDQ and associated elements should also intercept spurious particles in the beam abort gap to prevent quenches from occurring during regular beam aborts, and must also intercept the particles from the secondary halo during low beam lifetime without provoking quenches. In this note the conceptual design of the TCDQ system is briefly presented, with the load conditions and performance criteria. The FLUKA energy deposition simulations are described, and the results discussed in the context of the expected performance levels for LHC operation, in particular for the problems associated with quenching the downstream superconducting Q4 magnet. Optio...

  11. Numerical modeling for dilute and dense sprays

    Science.gov (United States)

    Chen, C. P.; Kim, Y. M.; Shang, H. M.; Ziebarth, J. P.; Wang, T. S.

    1992-01-01

    We have successfully implemented a numerical model for spray-combustion calculations. In this model, the governing gas-phase equations in Eulerian coordinate are solved by a time-marching multiple pressure correction procedure based on the operator-splitting technique. The droplet-phase equations in Lagrangian coordinate are solved by a stochastic discrete particle technique. In order to simplify the calculation procedure for the circulating droplets, the effective conductivity model is utilized. The k-epsilon models are utilized to characterize the time and length scales of the gas phase in conjunction with turbulent modulation by droplets and droplet dispersion by turbulence. This method entails random sampling of instantaneous gas flow properties and the stochastic process requires a large number of computational parcels to produce the satisfactory dispersion distributions even for rather dilute sprays. Two major improvements in spray combustion modelings were made. Firstly, we have developed a probability density function approach in multidimensional space to represent a specific computational particle. Secondly, we incorporate the Taylor Analogy Breakup (TAB) model for handling the dense spray effects. This breakup model is based on the reasonable assumption that atomization and drop breakup are indistinguishable processes within a dense spray near the nozzle exit. Accordingly, atomization is prescribed by injecting drops which have a characteristic size equal to the nozzle exit diameter. Example problems include the nearly homogeneous and inhomogeneous turbulent particle dispersion, and the non-evaporating, evaporating, and burning dense sprays. Comparison with experimental data will be discussed in detail.

  12. DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS

    Energy Technology Data Exchange (ETDEWEB)

    Kishore K. Mohanty

    2005-01-01

    There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. Imbibition in an originally oil-wet 2D capillary is the fastest in the case of Alf-38 and slowest in the case of DTAB (among the surfactants studied). Force of adhesion studies and contact angle measurements show that greater wettability alteration is possible with these anionic surfactants than the cationic surfactant studied. The water imbibition rate does not increase monotonically with an increase in the surfactant concentration. A numerical model has been developed that fits the rate of imbibition. Plans for the next quarter include conducting simulation and imbibition studies.

  13. Aqueous Angiography: Real-Time and Physiologic Aqueous Humor Outflow Imaging.

    Directory of Open Access Journals (Sweden)

    Sindhu Saraswathy

    Full Text Available Trabecular meshwork (TM bypass surgeries attempt to enhance aqueous humor outflow (AHO to lower intraocular pressure (IOP. While TM bypass results are promising, inconsistent success is seen. One hypothesis for this variability rests upon segmental (non-360 degrees uniform AHO. We describe aqueous angiography as a real-time and physiologic AHO imaging technique in model eyes as a way to simulate live AHO imaging.Pig (n = 46 and human (n = 6 enucleated eyes were obtained, orientated based upon inferior oblique insertion, and pre-perfused with balanced salt solution via a Lewicky AC maintainer through a 1mm side-port. Fluorescein (2.5% was introduced intracamerally at 10 or 30 mm Hg. With an angiographer, infrared and fluorescent (486 nm images were acquired. Image processing allowed for collection of pixel information based on intensity or location for statistical analyses. Concurrent OCT was performed, and fixable fluorescent dextrans were introduced into the eye for histological analysis of angiographically active areas.Aqueous angiography yielded high quality images with segmental patterns (p<0.0001; Kruskal-Wallis test. No single quadrant was consistently identified as the primary quadrant of angiographic signal (p = 0.06-0.86; Kruskal-Wallis test. Regions of high proximal signal did not necessarily correlate with regions of high distal signal. Angiographically positive but not negative areas demonstrated intrascleral lumens on OCT images. Aqueous angiography with fluorescent dextrans led to their trapping in AHO pathways.Aqueous angiography is a real-time and physiologic AHO imaging technique in model eyes.

  14. Magneto-hydrodynamic detection of vortex shedding for molten salt flow sensing.

    Energy Technology Data Exchange (ETDEWEB)

    Kruizenga, Alan Michael; Crocker, Robert W.

    2012-09-01

    High temperature flow sensors must be developed for use with molten salts systems at temperatures in excess of 600ÀC. A novel magneto-hydrodynamic sensing approach was investigated. A prototype sensor was developed and tested in an aqueous sodium chloride solution as a surrogate for molten salt. Despite that the electrical conductivity was a factor of three less than molten salts, it was found that the electrical conductivity of an electrolyte was too low to adequately resolve the signal amidst surrounding noise. This sensor concept is expected to work well with any liquid metal application, as the generated magnetic field scales proportionately with electrical conductivity.

  15. Sulfomethylated lignite salt as a sacrifical agent in oil recovery processes

    Energy Technology Data Exchange (ETDEWEB)

    Kudchadker, M.V.; Weiss, W.J.

    1978-02-07

    A process is described for recovering petroleum from oil reservoirs by secondary recovery methods. The process involves injecting via an injection well into the reservoir an aqueous solution of sulfomethylated lignite salt as a sacrificial agent to inhibit the deposition of surfactant and polymer on the reservoir matrix. The process is conducted by first injecting the lignite salt into the formation through the injection well and following it with either a polymer or a surfactant solution, which also may contain the lignite salt. The polymer or surfactant would then be followed by a drive fluid, such as water, to push the chemicals and oil to the production well. (18 claims)

  16. Lowering Salt in Your Diet

    Science.gov (United States)

    ... sodium, per serving. back to top Q. Are salt substitutes safe? A. Many salt substitutes contain potassium chloride and can be used by ... heart disease. Check with your doctor before using salt substitutes. back to top Q. What is FDA's role ...

  17. X-ray absorption spectroscopy of diluted system by undulator photon source and multi-element solid-state detector

    CERN Document Server

    Tanida, H

    2001-01-01

    In order to measure the extended X-ray absorption fine structure (EXAFS) spectrum of an ultra-diluted system, an optics and detector control system for a synchrotron radiation beamline is developed. The undulator gap width is continuously tuned to obtain the maximum X-ray photon flux during the energy scan for the EXAFS measurement. A piezoelectric translator optimizes the parallelism of the double crystal in a monochromator at each measurement point to compensate for mechanical errors of the monochromator, resulting in a smooth and intense X-ray photon flux during the measurement. For a detection of a weak fluorescence signal from diluted samples, a 19-element solid-state detector and digital signal processor are used. A K-edge EXAFS spectrum of iron in a myoglobin aqueous solution with a concentration of 5.58 parts per million was obtained by this system.

  18. COMPARISON BETWEEN TWO URINE DILUTION TESTS: THEIR ADVANTAGES AND DISADVANTAGES

    Directory of Open Access Journals (Sweden)

    Musso CG

    2015-05-01

    Full Text Available The main physiological test currently used for evaluating renal dilution capability is the hypotonic infusion test (HIT, which also evaluates proximal and thick ascending limb of Henle´s loops (TALH function. There is another urine dilution test: oral water load test, and it is simpler than HIT. However, it has not been documented yet if oral water load test performs an adequate evaluation of proximal tubule and TAHL activity, as HIT does. Thus, we decided to evaluate if there was any significant difference between both tests by evaluating: maximum urinary dilution capability, proximal sodium clearance, and TAHL sodium reabsorption. Materials and Method: Both urine dilution evaluating tests were prospectively performed to forty healthy volunteers with the aim of measuring the following physiological parameters by them: maximum urine hypotonicity, free water clearance, proximal tubule sodium clearance, and TALH sodium reabsorption. Results: All volunteers were able to maximally dilute their urine during HIT, while only 4 volunteers (10% were not able to do it during the oral water load tests. No significant difference was documented in the three studied parameters between both tests, in those patients who were able to maximally dilute their urine (n: 36 (p= NS. In conclusion this study has documented that HIT and oral water load test showed to be adequate studies for evaluating urine dilution capability, proximal and TAHL function. However, while HIT was more effective in obtaining the maximal dilution status, the oral water load test showed to be a simpler study.

  19. Dilution in Transition Zone between Rising Plumes and Surface Plumes

    DEFF Research Database (Denmark)

    Larsen, Torben

    2004-01-01

    The papers presents some physical experiments with the dilution of sea outfall plumes with emphasize on the transition zone where the relative fast flowing vertical plume turns to a horizontal surface plume following the slow sea surface currents. The experiments show that a considerable dilution...

  20. Dilution of Dense Bottom Plumes in Turbulent Currents

    DEFF Research Database (Denmark)

    Petersen, Ole; Larsen, Torben

    1994-01-01

    The dilution of negatively buoyant discharges released into a turbulent current has been studied both in the laboratory and by means of advanced numerical models. The experiments showed that the dilution is mainly due to vertical turbulent mixing and depends on a buoyancy induced dispersion...

  1. Sibship Size and Gendered Resource Dilution in Different Societal Contexts

    NARCIS (Netherlands)

    Kalmijn, M.; van de Werfhorst, H.G.

    2016-01-01

    Resource dilution theory hypothesizes that children’s educational attainment suffers from being raised with many siblings, as the parental resources have to be shared with more children. Based on economic and cultural theories, we hypothesize that resource dilution is gendered: especially a larger n

  2. Efficacy comparison between simple mixed-dilution and simple mid-dilution on-line hemodiafiltration techniques: a crossover study.

    Science.gov (United States)

    Susantitaphong, Paweena; Tiranathanagul, Khajohn; Katavetin, Pisut; Hanwiwatwong, Orawadee; Wittayalertpanya, Supeecha; Praditpornsilpa, Kearkiat; Tungsanga, Kriang; Eiam-Ong, Somchai

    2012-12-01

    Mid-dilution and mixed-dilution on-line hemodiafiltration (OL-HDF) techniques are innovated to overcome the limitations of two standard techniques including predilution and postdilution. Unfortunately, the head-to-head comparisons between these two novel techniques in the same study are still limited. Moreover, the original mid-dilution and mixed-dilution OL-HDF need special dialyzers and special machines. In the present study, simple mid-dilution and simple mixed-dilution OL-HDF were settled with the aim for clinical use in general hemodialysis (HD) centers. The efficacies of uremic toxins removal between both modalities were measured and compared. This prospective randomized crossover study was conducted on 12 stable HD patients undergoing simple mixed-dilution and simple mid-dilution OL-HDF techniques. HD prescriptions were similar in both techniques. The dialysis efficacies were determined by calculating small- (urea, creatinine, and phosphate) and middle-molecule (beta-2 microglobulin [β2M]) removal. Moreover, potential complications such as high transmembrane pressure (TMP) and protein loss were also observed. Simple mixed-dilution OL-HDF provided significantly greater clearances of urea, creatinine, and β2M when compared with the simple mid-dilution OL-HDF techniques. Phosphate clearances in both techniques were comparable. In addition, TMP and dialysate albumin loss were not different. There were no intradialytic complications in both techniques. Simple mixed-dilution OL-HDF could provide greater efficacy for small- and middle-molecule clearances and acceptable potential risks, while phosphate removal is comparable.

  3. Salt supply to and significance of asymmetric salt diapirs

    DEFF Research Database (Denmark)

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

    2012-01-01

    Salt diapirs can be asymmetric both internally and externally reflecting their evolution history. As such, this asymmetry bear a significant amount of information about the differential loading (± lateral forces) and in turn the salt supply that have shaped the diapir. In two dimensions......, In this study we compare results of analogue and numerical models of diapirs with two natural salt diapris (Klodawa and Gorleben diapirs) to explain their salt supply and asymmetric evolution. In a NW-SE section, the Gorleben salt diapir possesses an asymmetric external geometry represented by a large...... southeastern overhang due to salt extrusion during Middle Cretaceous followed by its burial in Tertiary. This external asymmetry is also reflected in the internal configuration of the diapir which shows different rates of salt flow on the two halves of the structure. The asymmetric external and internal...

  4. Salt supply to and significance of asymmetric salt diapirs

    DEFF Research Database (Denmark)

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

    2012-01-01

    Salt diapirs can be asymmetric both internally and externally reflecting their evolution history. As such, this asymmetry bear a significant amount of information about the differential loading (± lateral forces) and in turn the salt supply that have shaped the diapir. In two dimensions......, In this study we compare results of analogue and numerical models of diapirs with two natural salt diapris (Klodawa and Gorleben diapirs) to explain their salt supply and asymmetric evolution. In a NW-SE section, the Gorleben salt diapir possesses an asymmetric external geometry represented by a large...... southeastern overhang due to salt extrusion during Middle Cretaceous followed by its burial in Tertiary. This external asymmetry is also reflected in the internal configuration of the diapir which shows different rates of salt flow on the two halves of the structure. The asymmetric external and internal...

  5. The dilution effect on the extinction of wall diffusion flame

    Directory of Open Access Journals (Sweden)

    Ghiti Nadjib

    2014-12-01

    Full Text Available The dynamic process of the interaction between a turbulent jet diffusion methane flame and a lateral wall was experimentally studied. The evolution of the flame temperature field with the Nitrogen dilution of the methane jet flame was examined. The interaction between the diffusion flame and the lateral wall was investigated for different distance between the wall and the central axes of the jet flame. The dilution is found to play the central role in the flame extinction process. The flame response as the lateral wall approaches from infinity and the increasing of the dilution rate make the flame extinction more rapid than the flame without dilution, when the nitrogen dilution rate increase the flame temperature decrease.

  6. Dynamic dilution exponent in monodisperse entangled polymer solutions

    DEFF Research Database (Denmark)

    Shahid, T.; Huang, Qian; Oosterlinck, F.

    2017-01-01

    We study and model the linear viscoelastic properties of several entangled semi-dilute and concentrated solutions of linear chains of different molar masses and at different concentrations dissolved in their oligomers. We discuss the dilution effect of the oligomers on the entangled long chains...... of the long chain extremities. Then we discuss the influence of the polymer concentration on the terminal relaxation time of the solutions and how this can be modelled by the enhanced contour length fluctuation process (CR-CLF). We point out that this larger dilution effect is not only a function...... of concentration but also depends on the molar mass of the chains. While the proposed approach successfully explains the viscoelastic properties of a large number of semi-dilute solutions of polymers in their own oligomers, important discrepancies are found for semi-dilute entangled polymers in small...

  7. Road deicing salt irreversibly disrupts osmoregulation of salamander egg clutches.

    Science.gov (United States)

    Karraker, Nancy E; Gibbs, James P

    2011-03-01

    It has been postulated that road deicing salts are sufficiently diluted by spring rains to ameliorate any physiological impacts to amphibians breeding in wetlands near roads. We tested this conjecture by exposing clutches of the spotted salamander (Ambystoma maculatum) to three chloride concentrations (1 mg/L, 145 mg/L, 945 mg/L) for nine days, then transferred clutches to control water for nine days, and measured change in mass at three-day intervals. We measured mass change because water uptake by clutches reduces risks to embryos associated with freezing, predation, and disease. Clutches in controls sequestered water asymptotically. Those in the moderate concentrations lost 18% mass initially and regained 14% after transfer to control water. Clutches in high concentration lost 33% mass and then lost an additional 8% after transfer. Our results suggest that spring rains do not ameliorate the effects of deicing salts in wetlands with extremely high chloride concentrations.

  8. Dilute oxygen combustion. Phase I report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-10-01

    A novel burner, in which fuel (natural gas) and oxidant (oxygen or air) are separately injected into a furnace, shows promise for achieving very low nitrogen oxide(s) (NO{sub x}) emissions for commercial furnace applications. The dilute oxygen combustion (DOC) burner achieves very low NO{sub x} through in-furnace dilution of the oxidant stream prior to combustion, resulting in low flame temperatures, thus inhibiting thermal NO{sub x} production. The results of a fundamental and applied research effort on the development of the DOC burner are presented. In addition, the results of a market survey detailing the potential commercial impact of the DOC system are disclosed. The fundamental aspects of the burner development project involved examining the flame characteristics of a natural gas turbulent jet in a high-temperature ({approximately}1366 K) oxidant (7-27% O{sub 2} vol. wet). Specifically, the mass entrainment rate, the flame lift-off height, the velocity field and major species field of the jet were evaluated as a function of surrounding-gas temperature and composition. The measured entrainment rate of the fuel jet decreased with increasing oxygen content in the surrounding high-temperature oxidant, and was well represented by the d{sup +} scaling correlation found in the literature. The measured flame lift-off height decreased with increasing oxygen content and increasing temperature of the surrounding gas. An increase in surrounding-gas oxygen content and/or temperature inhibited the velocity decay within the jet periphery as a function of axial distance as compared to isothermal turbulent jets. However, the velocity measurements were only broadly represented by the d{sup +} scaling correlation. Several DOC burner configurations were tested in a laboratory-scale furnace at a nominal firing rate of 185 kW ({approximately}0.63 MMBtu/h). The flue gas composition was recorded as a function of furnace nitrogen content, furnace temperature, burner geometric

  9. Dilute Oxygen Combustion Phase I Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Ryan, H.M.; Riley, M.F.; Kobayashi, H.

    1997-10-31

    A novel burner, in which fuel (natural gas) and oxidant (oxygen or air) are separately injected into a furnace, shows promise for achieving very low nitrogen oxide(s) (NOx) emissions for commercial furnace applications. The dilute oxygen combustion (DOC) burner achieves very low NOx through in-furnace dilution of the oxidant stream prior to combustion, resulting in low flame temperatures, thus inhibiting thermal NOx production. The results of a fundamental and applied research effort on the development of the DOC burner are presented. In addition, the results of a market survey detailing the potential commercial impact of the DOC system are disclosed. The fundamental aspects of the burner development project involved examining the flame characteristics of a natural gas turbulent jet in a high-temperature (~1366 K) oxidant (7-27% O2 vol. wet). Specifically, the mass entrainment rate, the flame lift-off height, the velocity field and major species field of the jet were evaluated as a function of surrounding-gas temperature and composition. The measured entrainment rate of the fuel jet decreased with increasing oxygen content in the surrounding high-temperature oxidant, and was well represented by the d+ scaling correlation found in the literature. The measured flame lift-off height decreased with increasing oxygen content and increasing temperature of the surrounding gas. An increase in surrounding-gas oxygen content and/or temperature inhibited the velocity decay within the jet periphery as a function of axial distance as compared to isothermal turbulent jets. However, the velocity measurements were only broadly represented by the d+ scaling correlation. Several DOC burner configurations were tested in a laboratory-scale furnace at a nominal firing rate of 185 kW (~0.63 MMBtu/h). The flue gas composition was recorded as a function of furnace nitrogen content, furnace temperature, burner geometric arrangement, firing rate, and fuel injection velocity. NOx emissions

  10. Dilute Oxygen Combustion Phase 2 Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Ryan, H.M.; Riley, M.F.; Kobayashi, H.

    2005-09-30

    A novel burner, in which fuel (natural gas) and oxidant (oxygen or air) are separately injected into a furnace, shows promise for achieving very low nitrogen oxide(s) (NOx) emissions for commercial furnace applications. The dilute oxygen combustion (DOC) burner achieves very low NOx through in-furnace dilution of the oxidant stream prior to combustion, resulting in low flame temperatures, thus inhibiting thermal NOx production. The results of a fundamental and applied research effort on the development of the DOC burner are presented. In addition, the results of a market survey detailing the potential commercial impact of the DOC system are disclosed. The fundamental aspects of the burner development project involved examining the flame characteristics of a natural gas turbulent jet in a high-temperature (~1366 K) oxidant (7-27% O2 vol. wet). Specifically, the mass entrainment rate, the flame lift-off height, the velocity field and major species field of the jet were evaluated as a function of surrounding-gas temperature and composition. The measured entrainment rate of the fuel jet decreased with increasing oxygen content in the surrounding high-temperature oxidant, and was well represented by the d+ scaling correlation found in the literature. The measured flame lift-off height decreased with increasing oxygen content and increasing temperature of the surrounding gas. An increase in surrounding-gas oxygen content and/or temperature inhibited the velocity decay within the jet periphery as a function of axial distance as compared to isothermal turbulent jets. However, the velocity measurements were only broadly represented by the d+ scaling correlation. Several DOC burner configurations were tested in a laboratory-scale furnace at a nominal firing rate of 185 kW (~0.63 MMBtu/h). The flue gas composition was recorded as a function of furnace nitrogen content, furnace temperature, burner geometric arrangement, firing rate, and fuel injection velocity. NOx emissions

  11. Effects of dietary dilution source and dilution level on feather damage, performance, behaviour, and litter condition in pullets

    NARCIS (Netherlands)

    Qaisrani, S.N.; Krimpen, van M.M.; Kwakkel, R.P.

    2013-01-01

    An experiment was conducted to investigate the effects of dietary dilution sources and levels on feather damage, performance, feeding behavior, and litter condition in rearing pullets. It was hypothesized that dietary dilution increases feeding-related behavior and improves feather condition, partic

  12. Effect of aqueous extract of Ipomoea carnea leaf on isolated frog and mouse heart.

    Science.gov (United States)

    Bachhav, K V; Burande, M D; Rangari, V D; Mehta, J K

    1999-11-01

    Ipomoea carnea fam. Convolvulaceae is a poisonous plant and its toxicity is supposed to be due to the cardiac and respiratory failure. The present paper describes the cardiac effect of aqueous extract of the fresh leaves of I. carnea using mouse and frog heart. The aqueous extract produced an initial blockade of isolated frog heart for 5-10 sec followed by dose dependent increase in both amplitude and rate that lasts up to 2 min. Atropine (1 microgram/ml) blocked the initial depressant phase and potentiated the stimulant effect of the aqueous extract. The dose dependent increase in cardiac contractility of aqueous extract was not altered by propranolol or calcium channel blockers like nifedipine or diltiazem. The decrease in sodium chloride concentration or increase in potassium chloride concentration or calcium chloride concentration in physiological salt solution inhibited the responses to aqueous extract while an increase in sodium chloride concentration or decrease in potassium chloride or calcium chloride concentration in physiological salt solution potentiated the responses to the aqueous extract of I. carnea. It may be suggested from the data that aqueous extract of I. carnea produces positive inotropic effect on isolate frog heart possibly by sodium extrusion or release of the intracellular calcium.

  13. Mixed salt crystallisation fouling

    CERN Document Server

    Helalizadeh, A

    2002-01-01

    The main purpose of this investigation was to study the mechanisms of mixed salt crystallisation fouling on heat transfer surfaces during convective heat transfer and sub-cooled flow boiling conditions. To-date no investigations on the effects of operating parameters on the deposition of mixtures of calcium sulphate and calcium carbonate, which are the most common constituents of scales formed on heat transfer surfaces, have been reported. As part of this research project, a substantial number of experiments were performed to determine the mechanisms controlling deposition. Fluid velocity, heat flux, surface and bulk temperatures, concentration of the solution, ionic strength, pressure and heat transfer surface material were varied systematically. After clarification of the effect of these parameters on the deposition process, the results of these experiments were used to develop a mechanistic model for prediction of fouling resistances, caused by crystallisation of mixed salts, under convective heat transfer...

  14. Extensional Relaxation Times and Pinch-off Dynamics of Dilute Polymer Solutions

    Science.gov (United States)

    Dinic, Jelena; Zhang, Yiran; Jimenez, Leidy; Sharma, Vivek

    2015-11-01

    We show that visualization and analysis of capillary-driven thinning and pinch-off dynamics of the columnar neck in an asymmetric liquid bridge created by dripping-onto-substrate can be used for characterizing the extensional rheology of complex fluids. Using a particular example of dilute, aqueous PEO solutions, we show the measurement of both the extensional relaxation time and extensional viscosity of weakly elastic, polymeric complex fluids with low shear viscosity ηsessile drop to a nozzle is detected optically, and the extensional response for viscoelastic fluids is characterized by analyzing their elastocapillary self-thinning, we refer to this technique as optically-detected elastocapillary self-thinning dripping-onto-substrate (ODES-DOS) extensional rheometry.

  15. Hydrophobically modified polyelectrolytes I. Dilute solution properties of fluorocarbon-containingpoly(acrylic acid)

    Institute of Scientific and Technical Information of China (English)

    ZHOU, Hui(周晖); SONG, Guo-Qiang(宋国强); ZHANG, Yun-Xiang(章云祥); DIEING, Reinhold; MA, Lian; HAEUSSLING, Lukas

    2000-01-01

    Dilute solution viscosity of fluorocarbon-containing hydrophobically modified poly(acrylic acid) was measured in aqueous solutions of various NaCl concentrations. The intrinsic viscosity ([η]) and Huggins coefficient (kH) were evaluated using Huggins equations. It is found that, at low NaCl concentration, the modified polymers exhibit values of intrinsic viscosity ( [η] ) and Huggins coefficient (kH) similar to those of unmodified polymers. For both of the modified and unmodified polymers, the intrinsic viscosity decreases with increase of NaCl concentration, while the Huggins coefficient increases upon addition of NaCl. But the variation of [η] and kH is more significant for the modified polymers, which reflects the enhanced intra- and intermolecular hydrophobic association at higher NaCl concentration.

  16. Thermochemical Properties of Nicotine Salts

    Directory of Open Access Journals (Sweden)

    Riggs DM

    2014-12-01

    Full Text Available The thermal gravimetric analysis (TGA and differential scanning calorimetry (DSC results presented in this report clearly show that the thermal stability and the endothermic peak nicotine release temperatures are different for different nicotine salts and these temperatures appear to be linked to the general microstructural details of the salt itself. In addition, the peak nicotine release temperatures are highly dependent upon the sample size used. The heat of vaporization for neat (non-protonated nicotine is also sample-size dependent. The TGA data showed that the least stable of the salts tested at elevated temperatures was the liquid salt nicotine triacetate followed by the crystalline materials (e.g., nicotine gallate and finally, the amorphous salts (e.g., nicotine alginate. The DSC results revealed that the liquid and crystalline salts exhibit nicotine release endotherms that are strongly related to the sample weight being tested. The amorphous salts show nicotine endotherm peak temperatures that are nearly independent of the sample weight. The range of peak nicotine release temperatures varied depending upon the specific salts and the sample size from 83 oC to well over 200 oC. Based on these results, the evolution of nicotine from the nicotine salt should be expected to vary based on the composition of the salt, the details of its microstructure, and the amount of nicotine salt tested.

  17. Frost formation with salt

    OpenAIRE

    Guadarrama-Cetina, J.; Mongruel, A; González-Viñas, W; Beysens, D. A.

    2015-01-01

    The formation of frost in presence of salt (NaCl) crystal is experimentally investigated on a hydrophobic surface. It presents several remarkable features due to the interplay of salty-water saturation pressure evolution, initially lower than the saturation pressure of ice and water, and the percolating propagation of ice dendrites from defects throughout the supercooled water droplet pattern. In particular, it is remarkable that nucleation of supercooled water and/or ice is prevented around ...

  18. Increased chloride concentration in a lake due to deicing salt application.

    Science.gov (United States)

    Thunqvist, E L

    2003-01-01

    During winter, the Swedish National Road Administration uses on average 250,000 tonnes of sodium chloride for deicing purposes. Chloride concentration is a function of the amount of deicing salt applied during the winter season and the amount of water in which the salt can be diluted. An estimation of seasonal amount of deicing salt in relation to amount of run-off was used in order to identify the effects of deicing salt. The measured chloride concentration in a lake used as a municipal water supply was similar to the concentration estimated by a simple steady state method accounting for the catchment area. The simplified steady state method was a useful tool for estimating steady state concentrations on a regional level, including a non-influenced lake as a comparison.

  19. Molecular Thermodynamic Model for Polyelectrolyte Solutions with Added Salts%含盐聚电解质溶液的分子热力学模型

    Institute of Scientific and Technical Information of China (English)

    张波; 蔡钧; 刘洪来; 胡英

    2002-01-01

    A molecular thermodynamic model of polyelectrolyte developed previously was extended to polyelectrolyte solutions with added salts. Thermodynamic properties, such as activity coefficients of polyelectrolytes or added salts and osmotic coefficients of solvent, of a number of aqueous mixtures of polyelectrolytes and salts are analyzed with the proposed model. Successful correlation is obtained in the range of moderate or higher polyion concentration. For the same sample, thermodynamic properties of polyelectrolytes with and without simple electrolytes can be predicted mutually using parameters from regression data.

  20. Salting-out effects by pressure-corrected 3D-RISM

    Science.gov (United States)

    Misin, Maksim; Vainikka, Petteri A.; Fedorov, Maxim V.; Palmer, David S.

    2016-11-01

    We demonstrate that using a pressure corrected three-dimensional reference interaction site model one can accurately predict salting-out (Setschenow's) constants for a wide range of organic compounds in aqueous solutions of NaCl. The approach, based on classical molecular force fields, offers an alternative to more heavily parametrized methods.

  1. Effective interaction of charged platelets in aqueous solution: investigations of colloid laponite suspensions by static light scattering and small-angle x-ray scattering.

    Science.gov (United States)

    Li, Li; Harnau, L; Rosenfeldt, S; Ballauff, M

    2005-11-01

    We study dilute aqueous solutions of charged disklike mineral particles (laponite) by a combination of static light scattering (SLS) and small-angle x-ray scattering (SAXS). Laponite solutions are known to form gels above a certain critical concentration that must be described as nonequilibrium states. Here we focus on the investigation by SLS and SAXS at concentrations below gelation (cLaponite platelets as well as the structure factor describing their interaction at finite concentration. A detailed analysis of the combined sets of data proves that the solutions are in a well-defined equilibrium state. Moreover, this analysis demonstrates the internal consistency and accuracy of the scattering functions obtained at finite concentrations. We find that laponite particles interact through an effective pair potential that is attractive on short range but repulsive on longer range. This finding demonstrates that Laponite solutions exhibit only a limited stability at the concentration of added salt used herein. Raising the ionic strength to 0.005M already leads to slow flocculation as is evidenced from the enhanced scattering intensity at smallest scattering angles. All data strongly suggest that the gelation occurring at higher concentration is related to aggregation.

  2. Standard practice for modified salt spray (fog) testing

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2009-01-01

    1.1 This practice covers and sets forth conditions for five modifications in salt spray (fog) testing for specification purposes. These are in chronological order of their development: 1.1.1 Annex A1, acetic acid-salt spray test, continuous. 1.1.2 Annex A2, cyclic acidified salt spray test. 1.1.3 Annex A3, seawater acidified test, cyclic (SWAAT). 1.1.4 Annex A4, SO2 salt spray test, cyclic. 1.1.5 Annex A5, dilute electrolyte cyclic fog dry test. 1.2 This practice does not prescribe the type of modification, test specimen or exposure periods to be used for a specific product, nor the interpretation to be given to the results. 1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to consult and establish appropriate safety and health practices and determine the applicabilit...

  3. High pressure phase transition and variation of elastic constants of diluted magnetic semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Varshney, Dinesh; Sharma, P.; Kaurav, N. [School of Physics, Vigyan Bhawan, Devi Ahilya University, Takshila Campus, Indore 452017 (India); Shah, S. [Department of Physics, P. M. B. Gujarati Science College, Indore-452001 (India); Singh, R.K. [M. P. Bhoj (Open) University, Shivaji Nagar, Bhopal-462016 (India)

    2004-11-01

    A theoretical study of the high-pressure phase transition and elastic behavior in diluted magnetic semiconductors Zn{sub 0.83}Mn{sub 0.17}Se, using a three-body interaction (TBI) potential caused by the electron-shell deformation of the overlapping ions is carried out. The estimated values of phase transition pressure and the vast volume discontinuity in pressure-volume (PV) phase diagram indicate the structural phase transition from zincblende (B3) to rock salt (B1). The variation of second-order elastic constants with pressure resembles that observed in some binary semiconductors. The inconsistency in the deduced value of pressure derivative of second order elastic constant with the available data is attributed to the fact that we derive expressions neglecting thermal effects and assuming the overlap repulsion significant only up to nearest neighbors. The vdW interaction is effective in obtaining the thermodynamical parameters such as Debye temperature, Gruneisen parameter, thermal expansion coefficient, compressibility as well phase stability in diluted magnetic semiconductors. It is revealed that TBI model has a promise to predict the phase transition pressure and the pressure variation of elastic constants of other semiconductors as well. (copyright 2004 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  4. Transition from dilute to concentrated electrokinetic behavior in the dielectric spectra of a colloidal suspension.

    Science.gov (United States)

    Beltramo, Peter J; Furst, Eric M

    2012-07-24

    Dielectric spectroscopy is used to measure the complex permittivity of 200 and 100 nm diameter polystyrene latex suspended in potassium chloride (KCl) solutions over the frequency range 10(4)-10(7) Hz as a function of particle volume fraction (ϕ) and ionic strength. Dilute suspension dielectric spectra are in excellent agreement with electrokinetic theory. A volume fraction dependence of the dielectric increment is observed for low electrolyte concentrations (0.01, 0.05, and 0.1 mM) above ϕ ≈ 0.02. This deviation from the dilute theory occurs at a critical frequency ω* that is a function of volume fraction, particle size, and ionic strength. The dielectric increment of suspensions at the highest salt concentration (1 mM) shows no volume fraction dependence up to ϕ = 0.09. Values of ω* are collapsed onto a master curve that accounts for the length and time scales of ion migration between neighboring particles. The measured conductivity increment is independent of volume fraction and agrees with theory after accounting for added counterions and nonspecific adsorption.

  5. Evaluation of method for phthalate extraction from milk related to milk dilution ratio

    Directory of Open Access Journals (Sweden)

    Milojković Danica S.

    2015-01-01

    Full Text Available Liquid-liquid extraction techniques were compared coupled with gas chromatography-mass spectrometry (GC-MS, for the extraction and the determination of four phthalates: dimethyl phthalate (DMP, di-n-butyl phthalate (DBP, benzyl butyl phthalate (BBP and di-(2-ethylhexyl phthalate (DEHP in six different kinds of milk-based samples. Extraction factors: sample preparation, organic solvent type and volume, salt effect, agitation and the extraction time were optimized. The ion of base peaks (m/z 149 for DBP, BBP and DEHP and m/z 163 for DMP for investigated phthalates were selected for the screening studies. The acquisition was performed at the selected ion monitoring mode. The MSD response for GC-MS phthalate calibration standards was linear between 0.25 and 2.50 μg mL-1 with calculated LODs between 0.01 μg mL-1 to 0.04 μg mL-1 and LOQs of 0.05 μg mL-1 to 0.12 μg mL-1, while repeatability was between 1.7 % to 4.9 % RSD. The study demonstrated an increase of the recovery of less polar phthalates in matrix milk standards by matrix dilution. Recovery for hydrophilic phthalates, like DMP, was not changed by matrix dilution and it was continuously low for the investigated method. Two spiking levels were tested for influence of matrix dilution on phthalate recovery, showed the same trend. [Projekat Ministarstva nauke Republike Srbije, br. 31060

  6. Preparation of Ultrafine Cobalt Powder by Chemical Reduction in Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Nanocrystalline cobalt powders have been prepared from aqueous solution by reducing their corresponding metal salts under suitable conditions. The experimental conditions have been studied in detail. X-ray powder diffraction patterns show that the cobalt powder is hexagonal crystallite. The average particle size of the ultrafine cobalt powder is 55 nm.

  7. Affinity partitioning of human antibodies in aqueous two-phase systems

    NARCIS (Netherlands)

    Rosa, P. A. J.; Azevedo, A. M.; Ferreira, I. F.; de Vries, J.; Korporaal, R.; Verhoef, H. J.; Visser, T. J.; Aires-Barros, M. R.

    2007-01-01

    The partitioning of human immunoglobulin (IgG) in a polymer-polymer and polymer-salt aqueous two-phase system (ATPS) in the presence of several functionalised polyethylene glycols (PEGs) was studied. As a first approach, the partition studies were performed with pure IgG using systems in which the t

  8. Method for separating water soluble organics from a process stream by aqueous biphasic extraction

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, D.J.; Mego, W.A.

    1999-09-07

    A method for separating water-miscible organic species from a process stream by aqueous biphasic extraction is provided. An aqueous biphase system is generated by contacting a process stream comprised of water, salt, and organic species with an aqueous polymer solution. The organic species transfer from the salt-rich phase to the polymer-rich phase, and the phases are separated. Next, the polymer is recovered from the loaded polymer phase by selectively extracting the polymer into an organic phase at an elevated temperature, while the organic species remain in a substantially salt-free aqueous solution. Alternatively, the polymer is recovered from the loaded polymer by a temperature induced phase separation (cloud point extraction), whereby the polymer and the organic species separate into two distinct solutions. The method for separating water-miscible organic species is applicable to the treatment of industrial wastewater streams, including the extraction and recovery of complexed metal ions from salt solutions, organic contaminants from mineral processing streams, and colorants from spent dye baths.

  9. Method for separating water soluble organics from a process stream by aqueous biphasic extraction

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, David J. (Naperville, IL); Mego, William A. (Naperville, IL)

    1999-01-01

    A method for separating water-miscible organic species from a process stream by aqueous biphasic extraction is provided. An aqueous biphase system is generated by contacting a process stream comprised of water, salt, and organic species with an aqueous polymer solution. The organic species transfer from the salt-rich phase to the polymer-rich phase, and the phases are separated. Next, the polymer is recovered from the loaded polymer phase by selectively extracting the polymer into an organic phase at an elevated temperature, while the organic species remain in a substantially salt-free aqueous solution. Alternatively, the polymer is recovered from the loaded polymer by a temperature induced phase separation (cloud point extraction), whereby the polymer and the organic species separate into two distinct solutions. The method for separating water-miscible organic species is applicable to the treatment of industrial wastewater streams, including the extraction and recovery of complexed metal ions from salt solutions, organic contaminants from mineral processing streams, and colorants from spent dye baths.

  10. Use of diluted urine for cultivation of Chlorella vulgaris.

    Science.gov (United States)

    Jaatinen, Sanna; Lakaniemi, Aino-Maija; Rintala, Jukka

    2016-01-01

    Our aim was to study the biomass growth of microalga Chlorella vulgaris using diluted human urine as a sole nutrient source. Batch cultivations (21 days) were conducted in five different urine dilutions (1:25-1:300), in 1:100-diluted urine as such and with added trace elements, and as a reference, in artificial growth medium. The highest biomass density was obtained in 1:100-diluted urine with and without additional trace elements (0.73 and 0.60 g L(-1), respectively). Similar biomass growth trends and densities were obtained with 1:25- and 1:300-diluted urine (0.52 vs. 0.48 gVSS L(-1)) indicating that urine at dilution 1:25 can be used to cultivate microalgal based biomass. Interestingly, even 1:300-diluted urine contained sufficiently nutrients and trace elements to support biomass growth. Biomass production was similar despite pH-variation from < 5 to 9 in different incubations indicating robustness of the biomass growth. Ammonium formation did not inhibit overall biomass growth. At the beginning of cultivation, the majority of the biomass consisted of living algal cells, while towards the end, their share decreased and the estimated share of bacteria and cell debris increased.

  11. Biodiversity inhibits parasites: Broad evidence for the dilution effect.

    Science.gov (United States)

    Civitello, David J; Cohen, Jeremy; Fatima, Hiba; Halstead, Neal T; Liriano, Josue; McMahon, Taegan A; Ortega, C Nicole; Sauer, Erin Louise; Sehgal, Tanya; Young, Suzanne; Rohr, Jason R

    2015-07-14

    Infectious diseases of humans, wildlife, and domesticated species are increasing worldwide, driving the need to understand the mechanisms that shape outbreaks. Simultaneously, human activities are drastically reducing biodiversity. These concurrent patterns have prompted repeated suggestions that biodiversity and disease are linked. For example, the dilution effect hypothesis posits that these patterns are causally related; diverse host communities inhibit the spread of parasites via several mechanisms, such as by regulating populations of susceptible hosts or interfering with parasite transmission. However, the generality of the dilution effect hypothesis remains controversial, especially for zoonotic diseases of humans. Here we provide broad evidence that host diversity inhibits parasite abundance using a meta-analysis of 202 effect sizes on 61 parasite species. The magnitude of these effects was independent of host density, study design, and type and specialization of parasites, indicating that dilution was robust across all ecological contexts examined. However, the magnitude of dilution was more closely related to the frequency, rather than density, of focal host species. Importantly, observational studies overwhelmingly documented dilution effects, and there was also significant evidence for dilution effects of zoonotic parasites of humans. Thus, dilution effects occur commonly in nature, and they may modulate human disease risk. A second analysis identified similar effects of diversity in plant-herbivore systems. Thus, although there can be exceptions, our results indicate that biodiversity generally decreases parasitism and herbivory. Consequently, anthropogenic declines in biodiversity could increase human and wildlife diseases and decrease crop and forest production.

  12. Molecular simulation study on Hofmeister cations and the aqueous solubility of benzene.

    Science.gov (United States)

    Ganguly, Pritam; Hajari, Timir; van der Vegt, Nico F A

    2014-05-22

    We study the ion-specific salting-out process of benzene in aqueous alkali chloride solutions using Kirkwood-Buff (KB) theory of solutions and molecular dynamics simulations with different empirical force field models for the ions and benzene. Despite inaccuracies in the force fields, the simulations indicate that the decrease of the Setchenow salting-out coefficient for the series NaCl > KCl > RbCl > CsCl is determined by direct benzene-cation correlations, with the larger cations showing weak interactions with benzene. Although ion-specific aqueous solubilities of benzene may be affected by indirect ion-ion, ion-water, and water-water correlations, too, these correlations are found to be unimportant, with little to no effect on the Setchenow salting-out coefficients of the various salts. We further considered LiCl, which is experimentally known to be a weaker salting-out agent than NaCl and KCl and, therefore, ranks at an unusual position within the Hofmeister cation series. The simulations indicate that hydrated Li(+) ions can take part of the benzene hydration shell while the other cations are repelled by it. This causes weaker Li(+) exclusion around the solute and a resulting, weaker salting-out propensity of LiCl compared to that of the other salts. Removing benzene-water and benzene-salt electrostatic interactions in the simulations does not affect this mechanism, which may therefore also explain the smaller effect of LiCl, as compared to that of NaCl or KCl, on aqueous solvation and hydrophobic interaction of nonpolar molecules.

  13. Cross-linked polyvinyl pyridine coated glass particle catalyst support and aqueous composition or polyvinyl pyridine adducted microspheres

    Science.gov (United States)

    Rembaum, Alan (Inventor); Gupta, Amitava (Inventor); Volksen, Willi (Inventor)

    1981-01-01

    Microspheres are produced by cobalt gamma radiation initiated polymerization of a dilute aqueous vinyl pyridine solution. Addition of cross-linking agent provides higher surface area beads. Addition of monomers such as hydroxyethylmethacrylate acrylamide or methacrylamide increases hydrophilic properties and surface area of the beads. High surface area catalytic supports are formed in the presence of controlled pore glass substrate.

  14. Selective production of hemicellulose-derived carbohydrates from wheat straw using dilute HCl or FeCl3 solutions under mild conditions. X-ray and thermo-gravimetric analysis of the solid residues.

    Science.gov (United States)

    Marcotullio, G; Krisanti, E; Giuntoli, J; de Jong, W

    2011-05-01

    The present work explores the combined production of hemicellulose-derived carbohydrates and an upgraded solid residue from wheat straw using a dilute-acid pretreatment at mild temperature. Dilute aqueous HCl solutions were studied at temperatures of 100 and 120°C, and they were compared to dilute FeCl(3) under the same conditions. Comparable yields of soluble sugars and acetic acid were obtained, affording an almost complete removal of pentoses when using 200 mM aqueous solutions at 120°C. The solid residues of pretreatment were characterized showing a preserved crystallinity of the cellulose, and a almost complete removal of ash forming matter other than Si. Results showed upgraded characteristic of the residues for thermal conversion applications compared to the untreated wheat straw.

  15. Aqueous two-phase system based on natural quaternary ammonium compounds for the extraction of proteins.

    Science.gov (United States)

    Zeng, Chao-Xi; Xin, Rui-Pu; Qi, Sui-Jian; Yang, Bo; Wang, Yong-Hua

    2016-02-01

    Aqueous two-phase systems, based on the use of natural quaternary ammonium compounds, were developed to establish a benign biotechnological route for efficient protein separation. In this study, aqueous two-phase systems of two natural resources betaine and choline with polyethyleneglycol (PEG400/600) or inorganic salts (K2 HPO4 /K3 PO4 ) were formed. It was shown that in the K2 HPO4 -containing aqueous two-phase system, hydrophobic interactions were an important driving force of protein partitioning, while protein size played a vital role in aqueous two-phase systems that contained polyethylene glycol. An extraction efficiency of more than 90% for bovine serum albumin in the betaine/K2 HPO4 aqueous two-phase system can be obtained, and this betaine-based aqueous two-phase system provided a gentle and stable environment for the protein. In addition, after investigation of the cluster phenomenon in the betaine/K2 HPO4 aqueous two-phase systems, it was suggested that this phenomenon also played a significant role for protein extraction in this system. The development of aqueous two-phase systems based on natural quaternary ammonium compounds not only provided an effective and greener method of aqueous two-phase system to meet the requirements of green chemistry but also may help to solve the mystery of the compartmentalization of biomolecules in cells.

  16. Biological efficacy and stability of diluted ticarcillin-clavulanic acid in the topical treatment of Pseudomonas aeruginosa infections.

    Science.gov (United States)

    Bateman, Fiona L; Moss, Susan M; Trott, Darren J; Shipstone, Michael A

    2012-04-01

    Topical compounded Timentin(®) diluted with an inactive vehicle has been reported to be effective in the treatment of otitis externa caused by Pseudomonas aeruginosa. The aims of this study were to determine the biological efficacy of Timentin(®) (ticarcillin and clavulanic acid) when diluted in the carrier vehicle Methopt(®) against P. aeruginosa and to determine the efficacy and stability of Timentin(®) aqueous stock concentrate solution. Timentin(®) stock concentrate was tested against four P. aeruginosa isolates on days 0, 7, 14, 21 and 28; then after 2, 3, 4, 5, 6, 9 and 12 months of storage at 4 or -20°C. The diluted Timentin(®)-Methopt(®) solutions were tested against all isolates after 0, 2, 4, 6, 8, 10, 12, 14, 17, 21, 24 and 28 days of storage at 24 or 4°C. Minimal inhibitory concentration (MIC) levels for all strains were determined using the broth microdilution method. The MIC of the stock solution remained relatively constant and acceptable throughout the study when stored at -20°C and was also acceptable for shorter time periods (6-9 months) when stored at 4°C. The MIC for the diluted Timentin(®)-Methopt(®) solution remained relatively constant and acceptable throughout the study for all four bacterial strains, with no difference between the solutions stored at 4 or 24°C. The results of this study indicate that storage of the Timentin(®) stock solution at -20°C does not compromise efficacy for at least 12 months and that Timentin(®) diluted in Methopt(®) was stable for 28 days when stored at either 4 or 24°C.

  17. Effect of the salting-out agent anion nature on the phase separation of a potassium salt-potassium bis(alkyl polyoxyethylene)phosphate-water systems

    Science.gov (United States)

    Elokhov, A. M.; Lesnov, A. E.; Kudryashova, O. S.

    2016-10-01

    The effect the salting-out agent anion nature has on the temperature and concentration intervals of the existence of the separation area is established by analyzing the phase diagrams of pseudoternary KCl (KBr, KI, KNO3, K2SO4, K4P2O7)-potassium bis(alkyl polyoxyethylene)phosphate (oxyphos B)-water systems. It is concluded that the anionic salting-out capability is reduced in the order P2O 7 4- > SO 4 2- > Cl- > Br‒> NO 7 4- > SO 3 - > I-. The thermodynamic parameters of phase separation used to interpret the results are calculated. The observed pattern of a change in the salting-out ability of the investigated salts relative to aqueous solutions of the surfactants is in good agreement with the lyotropic (Hofmeister) series.

  18. A daily salt balance model for stream salinity generation processes following partial clearing from forest to pasture

    Directory of Open Access Journals (Sweden)

    M. A. Bari

    2006-01-01

    Full Text Available We developed a coupled salt and water balance model to represent the stream salinity generation process following land use changes. The conceptual model consists of three main components with five stores: (i Dry, Wet and Subsurface Stores, (ii a saturated Groundwater Store and (iii a transient Stream zone Store. The Dry and Wet Stores represent the salt and water movement in the unsaturated zone and also the near-stream dynamic saturated areas, responsible for the generation of salt flux associated with surface runoff and interflow. The unsaturated Subsurface Store represents the salt bulge and the salt fluxes. The Groundwater Store comes into play when the groundwater level is at or above the stream invert and quantifies the salt fluxes to the Stream zone Store. In the stream zone module, we consider a 'free mixing' between the salt brought about by surface runoff, interflow and groundwater flow. Salt accumulation on the surface due to evaporation and its flushing by initial winter flow is also incorporated in the Stream zone Store. The salt balance model was calibrated sequentially following successful application of the water balance model. Initial salt stores were estimated from measured salt profile data. We incorporated two lumped parameters to represent the complex chemical processes like diffusion-dilution-dispersion and salt fluxes due to preferential flow. The model has performed very well in simulating stream salinity generation processes observed at Ernies and Lemon experimental catchments in south west of Western Australia. The simulated and observed stream salinity and salt loads compare very well throughout the study period with NSE of 0.7 and 0.4 for Ernies and Lemon catchment respectively. The model slightly over predicted annual stream salt load by 6.2% and 6.8%.

  19. Correlation and prediction of thermodynamic properties of nonelectrolytes at infinite dilution in water over very wide temperature and pressure ranges (2000 K and 10 GPa)

    Science.gov (United States)

    Plyasunov, Andrey V.

    2015-11-01

    Thermodynamic modeling of natural processes involving deep aqueous fluids requires the knowledge of the values of chemical potentials (the Gibbs energy) of aqueous species. An accurate prediction of thermodynamic properties at high T and P is a strong challenge. It is shown that geochemical models, including the well-known HKF-model, cannot be recommended for an indiscriminate use at supercritical temperatures to predict chemical potentials of nonelectrolytes at infinite dilution in water. Nevertheless, sufficiently accurate predictions of ϕ2∞ (the fugacity coefficients at infinite dilution in water) of aqueous nonelectrolytes up to 2000 K and water densities up to 1500 kg m-3, i.e. pressure up to 10-12 GPa, can be made relying on known theoretical relations valid at various parts of the phase diagram of water. In essence, the method, proposed in this work, consists in the interpolation of properties between two known limits: the first one, at low water densities, is defined by the values of the second virial coefficients for water-solute interactions, and the second, at high water densities - by predictions of the theory of a mixture of hard spheres. The interpolation at moderate temperatures (700-1300 K) and water densities (500-900 kg m-3) is simplified by sufficiently accurate predictions of properties using a semiempirical variant of a corresponding-states principle. Presented examples of the prediction of fugacity coefficients of "gases" at infinite dilution in water and of an aqueous solubility of corundum over very wide ranges of water densities/pressures demonstrate the potential and generality of the proposed methods of evaluating the thermodynamic properties of aqueous neutral compounds.

  20. Lanthanide salts solutions: representation of osmotic coefficients within the binding mean spherical approximation.

    Science.gov (United States)

    Ruas, Alexandre; Moisy, Philippe; Simonin, Jean-Pierre; Bernard, Olivier; Dufrêche, Jean-François; Turq, Pierre

    2005-03-24

    Osmotic coefficients of aqueous solutions of lanthanide salts are described using the binding mean spherical approximation (BIMSA) model based on the Wertheim formalism for association. The lanthanide(III) cation and the co-ion are allowed to form a 1-1 ion pair. Hydration is taken into account by introducing concentration-dependent cation size and solution permittivity. An expression for the osmotic coefficient, derived within the BIMSA, is used to fit data for a wide variety of lanthanide pure salt aqueous solutions at 25 degrees C. A total of 38 lanthanide salts have been treated, including perchlorates, nitrates, and chlorides. For most solutions, good fits could be obtained up to high ionic strengths. The relevance of the fitted parameters has been discussed, and a comparison with literature values has been made (especially the association constants) when available.

  1. Hofmeister effect of salt mixtures on thermo-responsive poly(propylene oxide)

    DEFF Research Database (Denmark)

    Moghaddam, Saeed Zajforoushan; Thormann, Esben

    2015-01-01

    of aqueous solutions of poly(propylene oxide) is affected by mixtures of ions with different location in the Hofmeister series. Our results show that the Hofmeister effects of pure salt species are not always linearly additive and that the relative effect of some ions can be reversed depending......The Hofmeister series is a classification of ions regarding their ability to stabilize or destabilize aqueous solutions of proteins, polymers and other molecules which are partly miscible with water. In this study, we employ differential scanning calorimetry to investigate how the stability...... on the composition of the salt mixture as well as by the absolute and relative concentration of the different species. We suggest that these results can lead to a better understanding of the potential role of the Hofmeister effect in regulation of biological processes, which does always take place in salt mixtures...

  2. Rheology of rock salt for salt tectonics modeling

    Directory of Open Access Journals (Sweden)

    Shi-Yuan Li

    2016-10-01

    Full Text Available Abstract Numerical modeling of salt tectonics is a rapidly evolving field; however, the constitutive equations to model long-term rock salt rheology in nature still remain controversial. Firstly, we built a database about the strain rate versus the differential stress through collecting the data from salt creep experiments at a range of temperatures (20–200 °C in laboratories. The aim is to collect data about salt deformation in nature, and the flow properties can be extracted from the data in laboratory experiments. Moreover, as an important preparation for salt tectonics modeling, a numerical model based on creep experiments of rock salt was developed in order to verify the specific model using the Abaqus package. Finally, under the condition of low differential stresses, the deformation mechanism would be extrapolated and discussed according to microstructure research. Since the studies of salt deformation in nature are the reliable extrapolation of laboratory data, we simplified the rock salt rheology to dislocation creep corresponding to power law creep (n = 5 with the appropriate material parameters in the salt tectonic modeling.

  3. Aqueous biphasic systems involving alkylsulfate-based ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Deive, Francisco J. [Instituto de Tecnologia Quimica e Biologica, UNL, Av. Republica, Apartado 127, 2780-901 Oeiras (Portugal); Department of Chemical Engineering, University of Vigo, P.O. Box 36310, Vigo (Spain); Rodriguez, Ana [Department of Chemical Engineering, University of Vigo, P.O. Box 36310, Vigo (Spain); Marrucho, Isabel M., E-mail: imarrucho@itqb.unl.pt [Instituto de Tecnologia Quimica e Biologica, UNL, Av. Republica, Apartado 127, 2780-901 Oeiras (Portugal); Rebelo, Luis P.N. [Instituto de Tecnologia Quimica e Biologica, UNL, Av. Republica, Apartado 127, 2780-901 Oeiras (Portugal)

    2011-11-15

    Highlights: > K{sub 3}PO{sub 4}, K{sub 2}CO{sub 3}, Na{sub 2}CO{sub 3}, and (NH{sub 4}){sub 2}SO{sub 4} act as phase promoter in aqueous solutions of ILs. > Remarkable influence of alkyl-chain length on solubility curves of alkylsulfate-based ILs. > Merchuck correlation was used for describing these systems. > {Delta}S{sub hyd} and Hofmeister series were used to discuss the different salting out effects. - Abstract: The specific effects of K{sub 3}PO{sub 4}, K{sub 2}CO{sub 3}, Na{sub 2}CO{sub 3}, and (NH{sub 4}){sub 2}SO{sub 4}, as high charge-density inorganic salts and thus inducers of the formation of aqueous biphasic systems (ABS) containing several ethyl-methylimidazolium alkylsulfate ionic liquids, C{sub 2}MIM C{sub n}SO{sub 4} (n = 2, 4, 6, or 8), have been assessed at T = 298.15 K. The results are analyzed in the light of the Hofmeister series. The influence of different alkyl chain lengths in the anion, together with the ability of the selected inorganic salts to induce the formation of ABS, is discussed. Phase diagrams have been determined through turbidimetry, including tie lines assignments from mass phase ratios according to the lever - arm rule. The Merchuck equation was satisfactorily used to correlate the solubility curve.

  4. Investigation and development of liquid-liquid extraction systems for the removal of pertechnetate from aqueous nuclear waste stream simulants

    Science.gov (United States)

    Gansle, Kristina Marie Rohal

    1998-11-01

    The solvent extraction behavior of perrhenate (ReO 4-) and pertechnetate (TcO4- ) from aqueous nuclear waste stream simulants was examined using the anion-exchange reagent Aliquat-336 nitrate. The extraction tendencies of ReO 4- followed those of TcO4- from both acidic and basic media, demonstrating that ReO4 - was a suitable nonradioactive surrogate for TcO4 -. For ICP-AES analysis of Re in high salt solutions, a V-groove nebulizer and 1:1 dilution of the sample and standards with 0.1% Triton X-100 surfactant reduced deposition of solids within the sample introduction system, thus minimizing memory effects. A new approach to waste remediation technology, Redox-Recyclable Extraction and Recovery (R2ER), was also studied. The redox-active species 1,1',3,3'-tetrakis(2-methyl-2-hexyl)ferrocene (HEP) was oxidized to its cationic form for extraction of TcO4 - or ReO4- from aqueous waste and reduced to its neutral form for recovery of the anion. The thermodynamics of liquid-liquid interfacial electron transfer for the oxidation/activation of HEP were shown to be controlled by three factors: the reduction potentials of the redox-active species in the aqueous and organic phases and the transfer of an ion across the liquid-liquid interface. The deactivation/reduction rate of HEP+NO3- by iron was affected by organic solvent diluent and improved by treating the iron with hexanes and 1 M HCl. The volume of solid secondary-waste in the R2ER cycle was reduced by a factor of 3000. In complete extraction/recovery cycles, HEP+NO3- in 2-nonanone removed greater than 99% TcO4- from the 101-SY, 103-SY, 1 M HCl and 1 M NaOH/1.5 M NaNO3 Hanford Tank waste simulants. Another redox-active extractant, bis(hydridotris(1-pyrazolyl)borato)iron(III) nitrate (FeTp2+NO3-), was also selective for ReO4- remediation from simulated aqueous waste. Organic solutions of the alkyl substituted ferricenium extractants were not stable in the presence of nucleophilic anions and/or reducing agents. HEP+NO3

  5. Aqueous Humor Dynamics: A Review

    Science.gov (United States)

    Goel, Manik; Picciani, Renata G; Lee, Richard K; Bhattacharya, Sanjoy K

    2010-01-01

    Glaucoma is a family of optic neuropathies which cause irreversible but potentially preventable vision loss. Vision loss in most forms of glaucoma is related to elevated IOP with subsequent injury to the optic nerve. Secretion of aqueous humor and regulation of its outflow are physiologically important processes for maintaining IOP in the normal range. Thus, understanding the complex mechanisms that regulate aqueous humor circulation is essential for management of glaucoma. The two main structures related to aqueous humor dynamics are the ciliary body and the trabecular meshwork (TM). Three mechanisms are involved in aqueous humor formation: diffusion, ultrafiltration and active secretion. Active secretion is the major contributor to aqueous humor formation. The aqueous humor flow in humans follows a circadian rhythm, being higher in the morning than at night. The aqueous humor leaves the eye by passive flow via two pathways - the trabecular meshwork and the uveoscleral pathway. In humans, 75% of the resistance to aqueous humor outflow is localized within the TM with the juxtacanalicular portion of the TM being the main site of outflow resistance. Glycosaminoglycan deposition in the TM extracellular matrix (ECM) has been suggested to be responsible for increased outflow resistance at this specific site whereas others have suggested deposition of proteins, such as cochlin, obstruct the aqueous humor outflow through the TM. The uveoscleral outflow pathway is relatively independent of the intraocular pressure and the proportion of aqueous humor exiting the eye via the uveoscleral pathway decreases with age. PMID:21293732

  6. Biological effects of high-diluted substances and periodic table of elements

    Directory of Open Access Journals (Sweden)

    Cloe Taddei-Ferretti

    2012-09-01

    Full Text Available Background and Aims. There are several experimental evidences for the effects of high-diluted substances (see e.g. C. Taddei-Ferretti, A. Cotugno 1997, on effects of high-diluted drugs on the prevention and control of mice teratogenicity induced by purine derivatives; N.C. Sukul, C. Taddei-Ferretti, S.P. Sinha Babu, A. De, B. Nandi, A. Sukul, R. Dutta-Nag 2000, on high-diluted Nux vomica countering alcohol-induced loss of righting reflex in toads. Also the physical characterization and mechanism of action of high-diluted drugs have been studied (see e.g. N.C. Sukul, A. Sukul, High dilution effects: Physical and biochemical basis 2004. However, further experimental researches are needed to clarify how physical characteristics of a drug are linked to its global biological effects. Considerations on some high-diluted mineral remedies will be developer here. Methods. In Organon, sect. 119, S. Hahnemann writes: «As certainly each species of plants is different from every other one with regard to external appearance, way of life and growth, taste and smell, and as certainly each mineral, each salt is different from the others with regard to external, internal, physical and chemical qualities [...], so certainly all these vegetal and mineral substances have pathogenetic – and thus also curative – effects different among themselves [...]». This statement may be taken as basis for considering the characteristics of some elements, as ordered in the periodic table, in relation to those of some high-diluted mineral remedies. Conclusions. The elements were previously ordered in the periodic table according to the atomic weight chemically determined, and later more precisely according to the atomic number (number of protons. Then also the electronic configuration was taken into account: properties depending on atomic mass and deep electrons are not periodical, while chemical and several physical properties

  7. Success, failure and ambiguity of the dilution effect among competitors.

    Science.gov (United States)

    Strauss, Alexander T; Civitello, David J; Cáceres, Carla E; Hall, Spencer R

    2015-09-01

    It remains challenging to predict variation in the magnitude of disease outbreaks. The dilution effect seeks to explain this variation by linking multiple host species to disease transmission. It predicts that disease risk increases for a focal host when host species diversity declines. However, when an increase in species diversity does not reduce disease, we are often unable to diagnose why. Here, we increase mechanistic and predictive clarity of the dilution effect with a general trait-based model of disease transmission in multi-host communities. Then, we parameterise and empirically test our model with a multi-generational case study of planktonic disease. The model-experiment combination shows that hosts that vary in competitive ability (R*) and potential to spread disease (R0 ) can produce three qualitatively disparate outcomes of dilution on disease: the dilution effect can succeed, fail, or be ambiguous/irrelevant.

  8. Separation processes using expulsion from dilute supercritical solutions

    Science.gov (United States)

    Cochran, Jr., Henry D.

    1993-01-01

    A process for separating isotopes as well as other mixtures by utilizing the behavior of dilute repulsive or weakly attractive elements of the mixtures as the critical point of the solvent is approached.

  9. EFFECT OF ADSORPTION ON THE VISCOSITY OF DILUTE POLYMER SOLUTION

    Institute of Scientific and Technical Information of China (English)

    Rong-shi Cheng; Yu-fang Shao; Ming-zhu Liu; Rong-qing Lu

    1999-01-01

    Careful measurements of the dilute solution viscosities of polyethylene glycol and polyvinyl alcohol in water were carried out. The reduced viscosities of both polymer solutions plot upward curves at extremely dilute concentration levels similar to the phenomena observed for many polymer solutions in the early 1950's. Upon observation of the changes of the flow times of pure water in and the wall surface wettability of the viscometer after measuring solution viscosity, a view was formed that the observed viscosity abnormality at extremely dilute concentration regions is solely due to the effect of adsorption of polymer chains onto the wall surface of viscometer. A theory of adsorption effect based on the Langmuir isotherms was proposed and a mathematical analysis for data treatment was performed. The theory could adequately describe the existing viscosity data. It seems necessary to correct the viscosity result of dilute polymer solutions measured by glass capillary viscometer by taking into account the effect of adsorption in all cases.

  10. A Cold Cycle Dilution Refrigerator for Space Applications Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The cold cycle dilution refrigerator is a continuous refrigerator capable of cooling to temperatures below 100 mK that makes use of a novel thermal magnetic pump....

  11. Inhibition of oil plume dilution in Langmuir ocean circulation

    National Research Council Canada - National Science Library

    Yang, Di; Chamecki, Marcelo; Meneveau, Charles

    2014-01-01

    Oil spills from deep‐water blowouts rise through and interact with the ocean mixed layer and Langmuir turbulence, leading to considerable diversity of oil slick dilution patterns observed on the ocean surface...

  12. The Carlina-type diluted telescope: Stellar fringes on Deneb

    CERN Document Server

    Coroller, H Le; Hespeels, F; Arnold, L; Andersen, T; Deram, P; Ricci, D; Berio, P; Blazit, A; Clausse, J-M; Guillaume, C; Meunier, J-P; Regal, X; Sottile, R

    2014-01-01

    Context. The performance of interferometers has largely been increased over the last ten years. But the number of observable objects is still limited due to the low sensitivity and imaging capability of the current facilities. Studies have been done to propose a new generation of interferometers. Aims. The Carlina concept studied at the Haute-Provence Observatory consists in an optical interferometer configured as a diluted version of the Arecibo radio telescope: above the diluted primary mirror made of fixed co-spherical segments, a helium balloon or cables suspended between two mountains and/or pylons, carries a gondola containing the focal optics. This concept does not require delay lines. Methods. Since 2003, we have been building a technical demonstrator of this diluted telescope. The main goals of this project were to find the opto-mechanical solutions to stabilize the optics attached under cables at several tens of meters above the ground, and to characterize this diluted telescope under real condition...

  13. Attentional sets influence perceptual load effects, but not dilution effects.

    Science.gov (United States)

    Benoni, Hanna; Zivony, Alon; Tsal, Yehoshua

    2014-01-01

    Perceptual load theory [Lavie, N. (1995). Perceptual load as a necessary condition for selective attention. Journal of Experimental Psychology: Human Perception and Performance, 21, 451-468.; Lavie, N., & Tsal, Y. (1994) Perceptual load as a major determinant of the locus of selection in visual attention. Perception & Psychophysics, 56, 183-197.] proposes that interference from distractors can only be avoided in situations of high perceptual load. This theory has been supported by blocked design manipulations separating low load (when the target appears alone) and high load (when the target is embedded among neutral letters). Tsal and Benoni [(2010a). Diluting the burden of load: Perceptual load effects are simply dilution effects. Journal of Experimental Psychology: Human Perception and Performance, 36, 1645-1656.; Benoni, H., & Tsal, Y. (2010). Where have we gone wrong? Perceptual load does not affect selective attention. Vision Research, 50, 1292-1298.] have recently shown that these manipulations confound perceptual load with "dilution" (the mere presence of additional heterogeneous items in high-load situations). Theeuwes, Kramer, and Belopolsky [(2004). Attentional set interacts with perceptual load in visual search. Psychonomic Bulletin & Review, 11, 697-702.] independently questioned load theory by suggesting that attentional sets might also affect distractor interference. When high load and low load were intermixed, and participants could not prepare for the presentation that followed, both the low-load and high-load trials showed distractor interference. This result may also challenge the dilution account, which proposes a stimulus-driven mechanism. In the current study, we presented subjects with both fixed and mixed blocks, including a mix of dilution trials with low-load trials and with high-load trials. We thus separated the effect of dilution from load and tested the influence of attentional sets on each component. The results revealed that whereas

  14. Electrochromic Salts, Solutions, and Devices

    Energy Technology Data Exchange (ETDEWEB)

    Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky, T. Mark (Los Alamos, NM)

    2008-11-11

    Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

  15. Electrochromic Salts, Solutions, and Devices

    Energy Technology Data Exchange (ETDEWEB)

    Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky, T. Mark (Los Alamos, NM)

    2008-10-14

    Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

  16. Electrochromic salts, solutions, and devices

    Energy Technology Data Exchange (ETDEWEB)

    Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky,7,064,212 T. Mark (Los Alamos, NM)

    2006-06-20

    Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

  17. Salt fluoridation and oral health

    Directory of Open Access Journals (Sweden)

    Thomas M. Marthaler

    2013-11-01

    Full Text Available The aim of this paper is to make known the potential of fluoridated salt in community oral health programs, particularly in South Eastern Europe. Since 1922, the addition of iodine to salt has been successful in Switzerland. Goiter is virtually extinct. By 1945, the cariesprotective effect of fluorides was well established. Based on the success of water fluoridation, a gynecologist started adding of fluoride to salt. The sale of fluoridated salt began in 1956 in the Swiss Canton of Zurich, and several other cantons followed suit. Studies initiated in the early seventies showed that fluoride, when added to salt, inhibits dental caries. The addition of fluoride to salt for human consumption was officially authorized in 1980-82. In Switzerland 85% of domestic salt consumed is fluoridated and 67% in Germany. Salt fluoridation schemes are reaching more than one hundred million in Mexico, Colombia, Peru and Cuba. The cost of salt fluoridation is very low, within 0.02 and 0.05 € per year and capita. Children and adults of the low socio-economic strata tend to have substantially more untreated caries than higher strata. Salt fluoridation is by far the cheapest method for improving oral health. Conclusions. Salt fluoridation has cariostatic potential like water fluoridation (caries reductions up to 50%. In Europe, meaningful percentages of users have been attained only in Germany (67% and Switzerland (85%. In Latin America, there are more than 100 million users, and several countries have arrived at coverage of 90 to 99%. Salt fluoridation is by far the cheapest method of caries prevention, and billions of people throughout the world could benefit from this method.

  18. Salts and Co-crystals of Theobromine and their phase transformations in water

    Indian Academy of Sciences (India)

    Palash Sanphui; Ashwini Nangia

    2014-09-01

    Theobromine, a xanthine derivative analogous to caffeine and theophylline, is an effective central nervous system stimulant. It has lower aqueous solubility than caffeine and theophylline. Salts of theobromine with hydrochloric acid, phosphoric acid, methanesulfonic acid, benzenesulfonic acid and -toluenesulfonic acid were prepared using liquid-assisted grinding (LAG). Proton transfer from the strong acid to the weak base imidazole N resulted in N+-H…O− hydrogen-bonded supramolecular assemblies of theobromine salts. The mesylate salt is polymorphic with amide N-H…O dimer and catemer synthons for the theobromine cations. A variable stoichiometry for phosphate salts (1:3 and 1:2.5) were observed with the latter being more stable. All new salts were characterized by FT-IR, PXRD, DSC and finally single crystal X-ray diffraction. In terms of stability, these salts transformed to theobromine within 1 h of dissolution in water. Remarkably, the besylate and tosylate salts are 88 and 58 times more soluble than theobromine, but they dissociated within 1 h. In contrast, theobromine co-crystals with gallic acid, anthranilic acid and 5-chlorosalicylic acid were found to be stable for more than 24 h in the aqueous slurry conditions, except malonic co-crystal which transformed to theobrominewithin 1 h.Water mediated phase transformation of theobromine salts and co-crystalmay be due to the incongruency (high solubility difference) between the components. These results suggest that even though traditional salts are highly soluble compared to co-crystals, co-crystals can be superior in terms of stability.

  19. Dilution Refrigeration of Multi-Ton Cold Masses

    CERN Document Server

    Wikus, P; CERN. Geneva

    2007-01-01

    Dilution refrigeration is the only means to provide continuous cooling at temperatures below 250 mK. Future experiments featuring multi-ton cold masses require a new generation of dilution refrigeration systems, capable of providing a heat sink below 10 mK at cooling powers which exceed the performance of present systems considerably. This thesis presents some advances towards dilution refrigeration of multi-ton masses in this temperature range. A new method using numerical simulation to predict the cooling power of a dilution refrigerator of a given design has been developed in the framework of this thesis project. This method does not only allow to take into account the differences between an actual and an ideal continuous heat exchanger, but also to quantify the impact of an additional heat load on an intermediate section of the dilute stream. In addition, transient behavior can be simulated. The numerical model has been experimentally verified with a dilution refrigeration system which has been designed, ...

  20. Fine particulate speciation profile and emission factor of municipal solid waste incinerator established by dilution sampling method.

    Science.gov (United States)

    Yang, Hsi-Hsien; Luo, Shao-Wei; Lee, Kuei-Ting; Wu, Jhin-Yan; Chang, Chun Wei; Chu, Pei Feng

    2016-08-01

    In this study, fine particulate matter (PM2.5) emitted from a municipal solid waste incinerator (MSWI) was collected using dilution sampling method. Chemical compositions of the collected PM2.5 samples, including carbon content, metal elements, and water-soluble ions, were analyzed. Traditional in-stack hot sampling was simultaneously conducted to compare the influences of dilution on PM2.5 emissions and the characteristics of the bonded chemical species. The results, established by a dilution sampling method, show that PM2.5 and total particulate matter (TPM) emission factors were 61.6 ± 4.52 and 66.1 ± 5.27 g ton-waste(-1), respectively. The average ratio of PM2.5/TPM is 0.93, indicating that more than 90% of PM emission from the MSWI was fine particulate. The major chemical species in PM2.5 included organic carbon (OC), Cl(-), NH4(+), elemental carbon (EC) and Si, which account for 69.7% of PM2.5 mass. OC was from the unburned carbon in the exhaust, which adsorbed onto the particulate during the cooling process. High Cl(-) emission is primarily attributable to wastes containing plastic bags made of polyvinyl chloride, salt in kitchen refuse and waste biomass, and so on. Minor species that account for 0.01-1% of PM2.5 mass included SO4(2-), K(+), Na, K, NO3(-), Al, Ca(2+), Zn, Ca, Cu, Fe, Pb, and Mg. The mean ratio of dilution method/in-stack hot method was 0.454. The contents of water-soluble ions (Cl(-), SO4(2-), NO3(-)) were significantly enriched in PM2.5 via gas-to-particle conversion in the dilution process. Results indicate that in-stack hot sampling would underestimate levels of these species in PM2.5. PM2.5 samples from a municipal solid waste incinerator (MSWI) were collected simultaneously by a dilution sampling technique and a traditional in-stack method. PM2.5 emission factors and chemical speciation profiles were established. Dilution sampling provides more reliable data than in-stack hot sampling. The results can be applied to estimate the PM2