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Sample records for in-cloud liquid water

  1. Active microorganisms thrive among extremely diverse communities in cloud water.

    Directory of Open Access Journals (Sweden)

    Pierre Amato

    Full Text Available Clouds are key components in Earth's functioning. In addition of acting as obstacles to light radiations and chemical reactors, they are possible atmospheric oases for airborne microorganisms, providing water, nutrients and paths to the ground. Microbial activity was previously detected in clouds, but the microbial community that is active in situ remains unknown. Here, microbial communities in cloud water collected at puy de Dôme Mountain's meteorological station (1465 m altitude, France were fixed upon sampling and examined by high-throughput sequencing from DNA and RNA extracts, so as to identify active species among community members. Communities consisted of ~103-104 bacteria and archaea mL-1 and ~102-103 eukaryote cells mL-1. They appeared extremely rich, with more than 28 000 distinct species detected in bacteria and 2 600 in eukaryotes. Proteobacteria and Bacteroidetes largely dominated in bacteria, while eukaryotes were essentially distributed among Fungi, Stramenopiles and Alveolata. Within these complex communities, the active members of cloud microbiota were identified as Alpha- (Sphingomonadales, Rhodospirillales and Rhizobiales, Beta- (Burkholderiales and Gamma-Proteobacteria (Pseudomonadales. These groups of bacteria usually classified as epiphytic are probably the best candidates for interfering with abiotic chemical processes in clouds, and the most prone to successful aerial dispersion.

  2. Mercury and trace elements in cloud water and precipitation collected on Mt. Mansfield, Vermont.

    Science.gov (United States)

    Malcolm, Elizabeth G; Keeler, Gerald J; Lawson, Sean T; Sherbatskoy, Timothy D

    2003-08-01

    The lack of high quality measurements of Hg and trace elements in cloud and fog water led to the design of a new collector for clean sequential sampling of cloud and fog water. Cloud water was collected during nine non-precipitating cloud events on Mt. Mansfield, VT in the northeastern USA between August 1 and October 31, 1998. Sequential samples were collected during six of these events. Mercury cloud water concentrations ranged from 7.5 to 71.8 ng l(-1), with a mean of 24.8 ng l(-1). Liquid water content explained about 60% of the variability in Hg cloud concentrations. Highest Hg cloud water concentrations were found to be associated with transport from the Mid-Atlantic and Ohio River Valley, and lowest concentrations with transport from the north of Mt. Mansfield out of Canada. Twenty-nine event precipitation samples were collected during the ten-week cloud sampling period near the base of Mt. Mansfield as part of a long-term deposition study. The Hg concentrations of cloud water were similar to, but higher on average (median of 12.5 ng l(-1)) than Hg precipitation concentrations (median of 10.5 ng l(-1)). Cloud and precipitation samples were analyzed for fifteen trace elements including Mg, Cu, Zn, As, Cd and Pb by ICP-MS. Mean concentrations were higher in cloud water than precipitation for elements with predominately anthropogenic, but not crustal origin in samples from the same source region. One possible explanation is greater in-cloud scavenging of crustal elements in precipitating than non-precipitating clouds, and greater below-cloud scavenging of crustal than anthropogenic aerosols.

  3. Water: The Strangest Liquid

    Energy Technology Data Exchange (ETDEWEB)

    Nilsson, Anders

    2009-02-24

    Water, H2O, is familiar to everyone - it shapes our bodies and our planet. But despite its abundance, water has remained a mystery, exhibiting many strange properties that are still not understood. Why does the liquid have an unusually large capacity to store heat? And why is it denser than ice? Now, using the intense X-ray beams from particle accelerators, investigations into water are leading to fundamental discoveries about the structure and arrangement of water molecules. This lecture will elucidate the many mysteries of water and discuss current studies that are revolutionizing the way we see and understand one of the most fundamental substances of life.

  4. Evaluation of trace elements contamination in cloud/fog water at an elevated mountain site in Northern China.

    Science.gov (United States)

    Liu, Xiao-huan; Wai, Ka-ming; Wang, Yan; Zhou, Jie; Li, Peng-hui; Guo, Jia; Xu, Peng-ju; Wang, Wen-xing

    2012-07-01

    Totally 117 cloud/fog water samples were collected at the summit of Mt. Tai (1534m a.s.l.)-the highest mountain in the Northern China Plain. The results were investigated by a combination of techniques including back trajectory model, regional air quality and dust storm models, satellite observations and Principal Component Analysis. Elemental concentrations were determined by Inductively Coupled Plasma Mass Spectrometry, with stringent quality control measures. Higher elemental concentrations were found at Mt. Tai compared with those reported by other overseas studies. The larger proportions and higher concentrations of toxic elements such as Pb and As in cloud/fog water compared with those in rainwater at Mt. Tai suggests higher potential hazards of cloud/fog water as a source of contamination in polluted areas to the ecosystem. Peak concentrations of trace elements were frequently observed during the onset of cloud/fog events when liquid water contents of cloud/fog water were usually low and large amount of pollutants were accumulated in the ambient air. Inverse relationship between elemental concentrations and liquid water contents were only found in the samples with high electrical conductivities and liquid water contents lower than 0.3gm(-3). Affected mainly by the emissions of steel industries and mining activities, air masses transported from south/southwest of Mt. Tai were frequently associated with higher elemental concentrations. The element Mn is attributed to play an important role in the acidity of cloud/fog water. The composition of cloud/fog water influenced by an Asian dust storm event was reported, which was seldom found in the literature. Copyright © 2012 Elsevier Ltd. All rights reserved.

  5. Water quality for liquid wastes

    International Nuclear Information System (INIS)

    Mizuniwa, Fumio; Maekoya, Chiaki; Iwasaki, Hitoshi; Yano, Hiroaki; Watahiki, Kazuo.

    1985-01-01

    Purpose: To facilitate the automation of the operation for a liquid wastes processing system by enabling continuous analysis for the main ingredients in the liquid wastes accurately and rapidly. Constitution: The water quality monitor comprises a sampling pipeway system for taking out sample water for the analysis of liquid wastes from a pipeway introducing liquid wastes to the liquid wastes concentrator, a filter for removing suspended matters in the sample water and absorption photometer as a water quality analyzer. A portion of the liquid wastes is passed through the suspended matter filter by a feedpump. In this case, sulfate ions and chloride ions in the sample are retained in the upper portion of a separation color and, subsequently, the respective ingredients are separated and leached out by eluting solution. Since the leached out ingredients form ferric ions and yellow complexes respectively, their concentrations can be detected by the spectrum photometer. Accordingly, concentration for the sodium sulfate and sodium chloride in the liquid wastes can be analyzed rapidly, accurately and repeatedly by which the water quality can be determined rapidly and accurately. (Yoshino, Y.)

  6. Electrically excited liquid water

    NARCIS (Netherlands)

    Wexler, A.D.

    2016-01-01

    Water is essential to a healthy and secure world. Developing new technologies which can take full advantage of the unique attributes of water is important for meeting the ever increasing global demand while reducing the production footprint. Water exhibits unexpected departures in more than 70

  7. Electrically excited liquid water

    NARCIS (Netherlands)

    Wexler, A.D.

    2016-01-01

    Water is essential to a healthy and secure world. Developing new technologies which can take full advantage of the unique attributes of water is important for meeting the ever increasing global demand while reducing the production footprint. Water exhibits unexpected departures in more than 70

  8. Thermodynamic constraint on the cloud liquid water feedback in climate models

    Science.gov (United States)

    Betts, Alan K.; HARSHVARDHAN

    1987-01-01

    The cloud liquid water feedback in climate models consists of the increase (decrease) in optical depth of clouds resulting from higher (lower) liquid water contents that might accompany tropospheric warming (cooling). The change in cloud liquid water with temperature is shown to depend on the rate of change of the slope of the moist adiabat with respect to temperature, and it is a strong function of temperature. The value of this rate of change in the tropics is about half that in mid and high latitudes and is much less than the value obtained by assuming that liquid water scales with the saturation mixing ratio.

  9. Sensitive method for the determination of different S(IV) species in cloud and fog water.

    Science.gov (United States)

    Lammel, G

    1996-08-01

    Suppressed ion chromatography has been applied to the determination of S(IV) species in cloud and fog water in the range 0.012-2.4 mg S(IV)-S/L. The samples have been preserved prior to storage and S(IV) species have been determined as hydroxy methanesulfonate (HMS) together with the low molecular weight carboxylic acid anions, formate and acetate. Samples have been divided and treated differently such that total S(IV) as well as the non-oxidizable fraction of S(IV) (as given by the reactivity with H(2)O(2), added in surplus) could be determined. The difference between the two corresponds to the S(IV) fraction subjected to oxididation, which is of paramount interest in cloud and fogwater chemistry.

  10. Electron affinity of liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Gaiduk, Alex P.; Pham, Tuan Anh; Govoni, Marco; Paesani, Francesco; Galli, Giulia

    2018-01-16

    Understanding redox and photochemical reactions in aqueous environments requires a precise knowledge of the ionization potential and electron affinity of liquid water. The former has been measured, but not the latter. We predict the electron affinity of liquid water and of its surface from first principles, coupling path-integral molecular dynamics with ab initio potentials, and many-body perturbation theory. Our results for the surface (0.8 eV) agree well with recent pump-probe spectroscopy measurements on amorphous ice. Those for the bulk (0.1–0.3 eV) differ from several estimates adopted in the literature, which we critically revisit. We show that the ionization potential of the bulk and surface are almost identical; instead their electron affinities differ substantially, with the conduction band edge of the surface much deeper in energy than that of the bulk. We also discuss the significant impact of nuclear quantum effects on the fundamental gap and band edges of the liquid.

  11. Lattice Boltzmann simulation of water isotope fractionation during ice crystal growth in clouds

    Science.gov (United States)

    Lu, Guoping; DePaolo, Donald J.

    2016-05-01

    We describe a lattice Boltzmann (LB) method for simulating water isotope fractionation during diffusion-limited ice crystal growth by vapor deposition from water-oversaturated air. These conditions apply to the growth of snow crystals in clouds where the vapor composition is controlled by the presence of both ice crystals and water droplets. Modeling of water condensation with the LB method has the advantage of allowing concentration fields to evolve based on local conditions so that the controls on grain shapes of the condensed phase can be studied simultaneously with the controls on isotopic composition and growth rate. Water isotope fractionation during snow crystal growth involves kinetic effects due to diffusion of water vapor in air, which requires careful consideration of the boundary conditions at the ice-vapor interface. The boundary condition is relatively simple for water isotopes because the molecular exchange rate for water at the interface is large compared to the crystal growth rate. Our results for the bulk crystal isotopic composition are consistent with simpler models using analytical solutions for radial geometry. However, the model results are sufficiently different for oxygen isotopes that they could affect the interpretation of D-excess values of snow and ice. The extent of vapor oversaturation plays a major role in determining the water isotope fractionation as well as the degree of dendritic growth. Departures from isotopic equilibrium increase at colder temperatures as diffusivity decreases. Dendritic crystals are isotopically heterogeneous. Isotopic variations within individual snow crystals could yield information on the microphysics of ice condensation as well as on the accommodation or sticking coefficient of water associated with vapor deposition. Our results are ultimately a first step in implementing LB models for kinetically controlled condensation or precipitation reactions, but needs to be extended also to cases where the

  12. Biogenic, urban, and wildfire influences on the molecular composition of dissolved organic compounds in cloud water

    Directory of Open Access Journals (Sweden)

    R. D. Cook

    2017-12-01

    Full Text Available Organic aerosol formation and transformation occurs within aqueous aerosol and cloud droplets, yet little is known about the composition of high molecular weight organic compounds in cloud water. Cloud water samples collected at Whiteface Mountain, New York, during August–September 2014 were analyzed by ultra-high-resolution mass spectrometry to investigate the molecular composition of dissolved organic carbon, with a focus on sulfur- and nitrogen-containing compounds. Organic molecular composition was evaluated in the context of cloud water inorganic ion concentrations, pH, and total organic carbon concentrations to gain insights into the sources and aqueous-phase processes of the observed high molecular weight organic compounds. Cloud water acidity was positively correlated with the average oxygen : carbon ratio of the organic constituents, suggesting the possibility for aqueous acid-catalyzed (prior to cloud droplet activation or during/after cloud droplet evaporation and/or radical (within cloud droplets oxidation processes. Many tracer compounds recently identified in laboratory studies of bulk aqueous-phase reactions were identified in the cloud water. Organosulfate compounds, with both biogenic and anthropogenic volatile organic compound precursors, were detected for cloud water samples influenced by air masses that had traveled over forested and populated areas. Oxidation products of long-chain (C10−12 alkane precursors were detected during urban influence. Influence of Canadian wildfires resulted in increased numbers of identified sulfur-containing compounds and oligomeric species, including those formed through aqueous-phase reactions involving methylglyoxal. Light-absorbing aqueous-phase products of syringol and guaiacol oxidation were observed in the wildfire-influenced samples, and dinitroaromatic compounds were observed in all cloud water samples (wildfire, biogenic, and urban-influenced. Overall, the cloud water molecular

  13. Biogenic, urban, and wildfire influences on the molecular composition of dissolved organic compounds in cloud water

    Science.gov (United States)

    Cook, Ryan D.; Lin, Ying-Hsuan; Peng, Zhuoyu; Boone, Eric; Chu, Rosalie K.; Dukett, James E.; Gunsch, Matthew J.; Zhang, Wuliang; Tolic, Nikola; Laskin, Alexander; Pratt, Kerri A.

    2017-12-01

    Organic aerosol formation and transformation occurs within aqueous aerosol and cloud droplets, yet little is known about the composition of high molecular weight organic compounds in cloud water. Cloud water samples collected at Whiteface Mountain, New York, during August-September 2014 were analyzed by ultra-high-resolution mass spectrometry to investigate the molecular composition of dissolved organic carbon, with a focus on sulfur- and nitrogen-containing compounds. Organic molecular composition was evaluated in the context of cloud water inorganic ion concentrations, pH, and total organic carbon concentrations to gain insights into the sources and aqueous-phase processes of the observed high molecular weight organic compounds. Cloud water acidity was positively correlated with the average oxygen : carbon ratio of the organic constituents, suggesting the possibility for aqueous acid-catalyzed (prior to cloud droplet activation or during/after cloud droplet evaporation) and/or radical (within cloud droplets) oxidation processes. Many tracer compounds recently identified in laboratory studies of bulk aqueous-phase reactions were identified in the cloud water. Organosulfate compounds, with both biogenic and anthropogenic volatile organic compound precursors, were detected for cloud water samples influenced by air masses that had traveled over forested and populated areas. Oxidation products of long-chain (C10-12) alkane precursors were detected during urban influence. Influence of Canadian wildfires resulted in increased numbers of identified sulfur-containing compounds and oligomeric species, including those formed through aqueous-phase reactions involving methylglyoxal. Light-absorbing aqueous-phase products of syringol and guaiacol oxidation were observed in the wildfire-influenced samples, and dinitroaromatic compounds were observed in all cloud water samples (wildfire, biogenic, and urban-influenced). Overall, the cloud water molecular composition depended on

  14. Liquid Water may Stick on Hydrophobic Surfaces

    Indian Academy of Sciences (India)

    IAS Admin

    Indian Institute of Technology Kharagpur, India. Liquid Water may Stick on Hydrophobic. Surfaces. Suman Chakraborty. Professor. Department of Mechanical Engineering, IIT Kharagpur, India. July, 2016 ...

  15. An extended Intelligent Water Drops algorithm for workflow scheduling in cloud computing environment

    Directory of Open Access Journals (Sweden)

    Shaymaa Elsherbiny

    2018-03-01

    Full Text Available Cloud computing is emerging as a high performance computing environment with a large scale, heterogeneous collection of autonomous systems and flexible computational architecture. Many resource management methods may enhance the efficiency of the whole cloud computing system. The key part of cloud computing resource management is resource scheduling. Optimized scheduling of tasks on the cloud virtual machines is an NP-hard problem and many algorithms have been presented to solve it. The variations among these schedulers are due to the fact that the scheduling strategies of the schedulers are adapted to the changing environment and the types of tasks. The focus of this paper is on workflows scheduling in cloud computing, which is gaining a lot of attention recently because workflows have emerged as a paradigm to represent complex computing problems. We proposed a novel algorithm extending the natural-based Intelligent Water Drops (IWD algorithm that optimizes the scheduling of workflows on the cloud. The proposed algorithm is implemented and embedded within the workflows simulation toolkit and tested in different simulated cloud environments with different cost models. Our algorithm showed noticeable enhancements over the classical workflow scheduling algorithms. We made a comparison between the proposed IWD-based algorithm with other well-known scheduling algorithms, including MIN-MIN, MAX-MIN, Round Robin, FCFS, and MCT, PSO and C-PSO, where the proposed algorithm presented noticeable enhancements in the performance and cost in most situations.

  16. Understanding the liquid-liquid (water-hexane) interface

    Science.gov (United States)

    Murad, Sohail; Puri, Ishwar K.

    2017-10-01

    Nonequilibrium molecular dynamics simulations are employed to investigate the interfacial thermal resistance of nanoscale hexane-water interfaces subject to an applied heat flux. Our studies show that these liquid-liquid interfaces exhibit behavior significantly dissimilar to that of solid-liquid and solid-vapor interfaces. Notably, the thermal resistance of a hexane-water interface is contingent on the interfacial temperature gradient alone with negligible dependence on the mean interfacial temperature, while the solid-liquid dependent strongly on the interfacial temperature. Application of a heat flux also increases the interface thickness significantly as compared to an equilibrium isothermal interface. Since liquid-liquid interfaces have been proposed for diverse applications, e.g., sensors for wastewater treatment and for extraction of toxic ions from water, they can be designed to be wider by applying a heat flux. This may allow the interface to be used for other applications not possible currently because of the very limited thickness of the interface in isothermal systems.

  17. (Liquid + liquid) equilibria of (water + lactic acid + alcohol) ternary systems

    Energy Technology Data Exchange (ETDEWEB)

    Sahin, Selin [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey); Ismail Kirbaslar, S. [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)], E-mail: krbaslar@istanbul.edu.tr; Bilgin, Mehmet [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)

    2009-01-15

    (Liquid + liquid) equilibrium (LLE) measurements of the solubility (binodal) curves and tie-line end compositions were carried out for {l_brace}water (1) + lactic acid (2) + octanol, or nonanol, or decanol (3){r_brace} at T = 298.15 K and 101.3 {+-} 0.7 kPa. The relative mutual solubility of lactic acid is higher in the water layers than in the organic layers. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The LLE results for the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  18. Radioactive liquid water processing method

    International Nuclear Information System (INIS)

    Yasumura, Keijiro; Noda, Tetsuya; Kobayashi, Fumio.

    1993-01-01

    Alkaline earth metals and heavy metals are added to radioactive liquid wastes containing a surface active agent comprising alkali metal salts of higher fatty acids. These metals form metal soaps with the surface active agent dissolved in the liquid wastes and crystallized. The crystallized metal soaps are introduced to a filtering column filled with a burnable polymeric fibrous filtering material. The filtering material is burnt. This can remove the surface active agent to remove COD without using an active carbon. (T.M.)

  19. (Liquid + liquid) equilibria of (water + butyric acid + esters) ternary systems

    International Nuclear Information System (INIS)

    Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet

    2007-01-01

    (Liquid + liquid) equilibrium (LLE) data of the solubility (binodal) curves and tie-line end compositions were examined for mixtures of {water (1) + butyric acid (2) + ethyl propionate or dimethyl phthalate or dibutyl phthalate (3)} at T = 298.15 K and (101.3 ± 0.7) kPa. The relative mutual solubility of the butyric acid is higher in the layers of esters than in the aqueous layer. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The LLE data of the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region

  20. (Liquid + liquid) equilibria of (water + propionic acid + alcohol) ternary systems

    Energy Technology Data Exchange (ETDEWEB)

    Kirbaslar, S. Ismail [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)]. E-mail: krbaslar@istanbul.edu.tr; Sahin, Selin [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey); Bilgin, Mehmet [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)

    2006-12-15

    (Liquid + liquid) equilibrium (LLE) data of the solubility (binodal) curves and tie-line end composition were examined for mixtures of {l_brace}water (1) + propionic acid (2) + octanol or nonanol or decanol or dodecanol (3){r_brace} at T = 298.15 K and 101.3 {+-} 0.7 kPa. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The LLE data of the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  1. Liquid Water may Stick on Hydrophobic Surfaces

    Indian Academy of Sciences (India)

    IAS Admin

    The behavior of fluid on a solid surface under static and dynamic conditions are usually clubbed together. • On a wetting surface (hydrophilic), liquid water is believed to adhere to the surface causing multilayer sticking. • On a non-wetting surface (hydrophobic), water is believed to glide across the surface leading to slip ...

  2. Liquid chromatographic determination of water

    Science.gov (United States)

    Fortier, N.E.; Fritz, J.S.

    1990-11-13

    A sensitive method for the determination of water in the presence of common interferences is presented. The detection system is based on the effect of water on the equilibrium which results from the reaction aryl aldehydes, such as cinnamaldehyde and methanol in the eluent to form cinnamaldehyde dimethylacetal, plus water. This equilibrium is shifted in a catalytic atmosphere of a hydrogen ion form past column reactor. The extent of the shift and the resulting change in absorbance are proportional to the amount of water present. 1 fig.

  3. Water Contaminant Mitigation in Ionic Liquid Propellant

    Science.gov (United States)

    Conroy, David; Ziemer, John

    2009-01-01

    Appropriate system and operational requirements are needed in order to ensure mission success without unnecessary cost. Purity requirements applied to thruster propellants may flow down to materials and operations as well as the propellant preparation itself. Colloid electrospray thrusters function by applying a large potential to a room temperature liquid propellant (such as an ionic liquid), inducing formation of a Taylor cone. Ions and droplets are ejected from the Taylor cone and accelerated through a strong electric field. Electrospray thrusters are highly efficient, precise, scaleable, and demonstrate low thrust noise. Ionic liquid propellants have excellent properties for use as electrospray propellants, but can be hampered by impurities, owing to their solvent capabilities. Of foremost concern is the water content, which can result from exposure to atmosphere. Even hydrophobic ionic liquids have been shown to absorb water from the air. In order to mitigate the risks of bubble formation in feed systems caused by water content of the ionic liquid propellant, physical properties of the ionic liquid EMI-Im are analyzed. The effects of surface tension, material wetting, physisorption, and geometric details of the flow manifold and electrospray emitters are explored. Results are compared to laboratory test data.

  4. Organic acids in cloud water and rainwater at a mountain site in acid rain areas of South China.

    Science.gov (United States)

    Sun, Xiao; Wang, Yan; Li, Haiyan; Yang, Xueqiao; Sun, Lei; Wang, Xinfeng; Wang, Tao; Wang, Wenxing

    2016-05-01

    To investigate the chemical characteristics of organic acids and to identify their source, cloud water and rainwater samples were collected at Mount Lu, a mountain site located in the acid rain-affected area of south China, from August to September of 2011 and March to May of 2012. The volume-weighted mean (VWM) concentration of organic acids in cloud water was 38.42 μeq/L, ranging from 7.45 to 111.46 μeq/L, contributing to 2.50 % of acidity. In rainwater samples, organic acid concentrations varied from 12.39 to 68.97 μeq/L (VWM of 33.39 μeq/L). Organic acids contributed significant acidity to rainwater, with a value of 17.66 %. Formic acid, acetic acid, and oxalic acid were the most common organic acids in both cloud water and rainwater. Organic acids had an obviously higher concentration in summer than in spring in cloud water, whereas there was much less discrimination in rainwater between the two seasons. The contribution of organic acids to acidity was lower during summer than during spring in both cloud water (2.20 % in summer vs 2.83 % in spring) and rainwater (12.24 % in summer vs 19.89 % in spring). The formic-to-acetic acid ratio (F/A) showed that organic acids were dominated by primary emissions in 71.31 % of the cloud water samples and whole rainwater samples. Positive matrix factorization (PMF) analysis determined four factors as the sources of organic acids in cloud water, including biogenic emissions (61.8 %), anthropogenic emissions (15.28 %), marine emissions (15.07 %) and soil emissions (7.85 %). The findings from this study imply an indispensable role of organic acids in wet deposition, but organic acids may have a limited capacity to increase ecological risks in local environments.

  5. Shallow Water Tuned Liquid Dampers

    DEFF Research Database (Denmark)

    Krabbenhøft, Jørgen

    researchers on TLDs termed wave breaking. A large part of the energy dissipation in the fluid is anticipated to stem from the turbulence in the vicinity of the moving hydraulic jump, and in order to verify this supposition the effect of bottom friction is included in the mathematical model. Studies reveal...... that for realistic roughness parameters the bottom friction has very limited effect on the liquid sloshing behavior and can be neglected. Herby the postulate is verified. Based on the mathematical model three dimensionless parameters are derived showing that the response of the damper depends solely on ratio...... of the base amplitude and tank length, A/L, on the frequency ratio of the forcing frequency and sloshing frequency, Ω/ωw, and finally on a friction parameter γ. These dimensionless parameters have been postulated by several researches in the field of TLDs but has not been derived rigorously as in the present...

  6. Temporal evolution of stable water isotopologues in cloud droplets in a hill cap cloud in central Europe (HCCT-2010

    Directory of Open Access Journals (Sweden)

    J. K. Spiegel

    2012-12-01

    Full Text Available In this work, we present the first study resolving the temporal evolution of δ2H and δ18O values in cloud droplets during 13 different cloud events. The cloud events were probed on a 937 m high mountain chain in Germany in the framework of the Hill Cap Cloud Thuringia 2010 campaign (HCCT-2010 in September and October 2010. The δ values of cloud droplets ranged from −77‰ to −15‰ (δ2H and from −12.1‰ to −3.9‰ (δ18O over the whole campaign. The cloud water line of the measured δ values was δ2H=7.8×δ18O+13×10−3, which is of similar slope, but with higher deuterium excess than other Central European Meteoric Water Lines. Decreasing δ values in the course of the campaign agree with seasonal trends observed in rain in central Europe. The deuterium excess was higher in clouds developing after recent precipitation revealing episodes of regional moisture recycling. The variations in δ values during one cloud event could either result from changes in meteorological conditions during condensation or from variations in the δ values of the water vapor feeding the cloud. To test which of both aspects dominated during the investigated cloud events, we modeled the variation in δ values in cloud water using a closed box model. We could show that the variation in δ values of two cloud events was mainly due to changes in local temperature conditions. For the other eleven cloud events, the variation was most likely caused by changes in the isotopic composition of the advected and entrained vapor. Frontal passages during two of the latter cloud events led to the strongest temporal changes in both δ2H (≈ 6‰ per hour and δ18O (≈ 0.6‰ per hour. Moreover, a detailed trajectory analysis for the two longest cloud events revealed that variations in the entrained vapor were most likely related to rain out or changes in relative

  7. Temporal evolution of stable water isotopologues in cloud droplets in a hill cap cloud in central Europe (HCCT-2010)

    Science.gov (United States)

    Spiegel, J.K.; Aemisegger, F.; Scholl, M.; Wienhold, F.G.; Collett, J.L.; Lee, T.; van Pinxteren, D.; Mertes, S.; Tilgner, A.; Herrmann, H.; Werner, Roland A.; Buchmann, N.; Eugster, W.

    2012-01-01

    In this work, we present the first study resolving the temporal evolution of δ2H and δ18O values in cloud droplets during 13 different cloud events. The cloud events were probed on a 937 m high mountain chain in Germany in the framework of the Hill Cap Cloud Thuringia 2010 campaign (HCCT-2010) in September and October 2010. The δ values of cloud droplets ranged from −77‰ to −15‰ (δ2H) and from −12.1‰ to −3.9‰ (δ18O) over the whole campaign. The cloud water line of the measured δ values was δ2H=7.8×δ18O+13×10−3, which is of similar slope, but with higher deuterium excess than other Central European Meteoric Water Lines. Decreasing δ values in the course of the campaign agree with seasonal trends observed in rain in central Europe. The deuterium excess was higher in clouds developing after recent precipitation revealing episodes of regional moisture recycling. The variations in δ values during one cloud event could either result from changes in meteorological conditions during condensation or from variations in the δ values of the water vapor feeding the cloud. To test which of both aspects dominated during the investigated cloud events, we modeled the variation in δ values in cloud water using a closed box model. We could show that the variation in δ values of two cloud events was mainly due to changes in local temperature conditions. For the other eleven cloud events, the variation was most likely caused by changes in the isotopic composition of the advected and entrained vapor. Frontal passages during two of the latter cloud events led to the strongest temporal changes in both δ2H (≈ 6‰ per hour) and δ18O (≈ 0.6‰ per hour). Moreover, a detailed trajectory analysis for the two longest cloud events revealed that variations in the entrained vapor were most likely related to rain out or changes in relative humidity and temperature at the moisture source region or both. This study illustrates the sensitivity of stable isotope

  8. Water: A Tale of Two Liquids

    Science.gov (United States)

    2016-01-01

    Water is the most abundant liquid on earth and also the substance with the largest number of anomalies in its properties. It is a prerequisite for life and as such a most important subject of current research in chemical physics and physical chemistry. In spite of its simplicity as a liquid, it has an enormously rich phase diagram where different types of ices, amorphous phases, and anomalies disclose a path that points to unique thermodynamics of its supercooled liquid state that still hides many unraveled secrets. In this review we describe the behavior of water in the regime from ambient conditions to the deeply supercooled region. The review describes simulations and experiments on this anomalous liquid. Several scenarios have been proposed to explain the anomalous properties that become strongly enhanced in the supercooled region. Among those, the second critical-point scenario has been investigated extensively, and at present most experimental evidence point to this scenario. Starting from very low temperatures, a coexistence line between a high-density amorphous phase and a low-density amorphous phase would continue in a coexistence line between a high-density and a low-density liquid phase terminating in a liquid–liquid critical point, LLCP. On approaching this LLCP from the one-phase region, a crossover in thermodynamics and dynamics can be found. This is discussed based on a picture of a temperature-dependent balance between a high-density liquid and a low-density liquid favored by, respectively, entropy and enthalpy, leading to a consistent picture of the thermodynamics of bulk water. Ice nucleation is also discussed, since this is what severely impedes experimental investigation of the vicinity of the proposed LLCP. Experimental investigation of stretched water, i.e., water at negative pressure, gives access to a different regime of the complex water diagram. Different ways to inhibit crystallization through confinement and aqueous solutions are

  9. (Liquid + liquid) equilibria of (water + butyric acid + esters) ternary systems

    Energy Technology Data Exchange (ETDEWEB)

    Kirbaslar, S. Ismail [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)], E-mail: krbaslar@istanbul.edu.tr; Sahin, Selin; Bilgin, Mehmet [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)

    2007-09-15

    (Liquid + liquid) equilibrium (LLE) data of the solubility (binodal) curves and tie-line end compositions were examined for mixtures of {l_brace}water (1) + butyric acid (2) + ethyl propionate or dimethyl phthalate or dibutyl phthalate (3){r_brace} at T = 298.15 K and (101.3 {+-} 0.7) kPa. The relative mutual solubility of the butyric acid is higher in the layers of esters than in the aqueous layer. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The LLE data of the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  10. Perspective on the structure of liquid water

    International Nuclear Information System (INIS)

    Nilsson, A.; Pettersson, L.G.M.

    2011-01-01

    Graphical abstract: Liquid water can be described in a fluctuating inhomogeneous picture with two local structural motifs that are spatially separated. At ambient temperatures most molecules favor a closer packing than tetrahedral, with strongly distorted hydrogen bonds giving higher density (yellow), which allows the quantized librational modes to be excited and contribute to the entropy, but with enthalpically favored tetrahedrally bonded water patches appearing as fluctuations (blue), i.e. a competition between entropy and enthalpy. Upon cooling water the amount of molecules participating in tetrahedral structures and the size of the tetrahedral patches increase. Highlights: ► Two components maximizing either enthalpy (tetrahedral, low-density) or entropy (non-specific H-bonding, higher density). ► Interconvert discontinuously and ratio depends on temperature. ► Density fluctuations on 1 nm length scale. ► Increasing size in supercooled region. ► Connection to Widom line and 2nd critical point. - Abstract: We present a picture that combines discussions regarding the thermodynamic anomalies in ambient and supercooled water with recent interpretations of X-ray spectroscopy and scattering data of water in the ambient regime. At ambient temperatures most molecules favor a closer packing than tetrahedral, with strongly distorted hydrogen bonds, which allows the quantized librational modes to be excited and contribute to the entropy, but with enthalpically favored tetrahedrally bonded water patches appearing as fluctuations, i.e. a competition between entropy and enthalpy. Upon cooling water the amount of molecules participating in tetrahedral structures and the size of the tetrahedral patches increase. The two local structures are connected to the liquid–liquid critical point hypothesis in supercooled water corresponding to high density liquid and low density liquid. We will discuss the interpretation of X-ray absorption spectroscopy, X-ray emission

  11. Optical properties and structure of liquid water

    International Nuclear Information System (INIS)

    Magat, M.; Reinisch, L.

    1975-01-01

    Information about the structure of liquid water arises from various experimental methods (X-ray and neutron diffraction, neutron scattering, dielectric dispersion, molecular dynamics and so on...). However, optical measurements (and especially spectroscopic ones) are particularly important in this connection. Recent results concerning the refraction index, the electronic absorption spectrum, the vibrational infrared and Raman spectra, the intermolecular modes in the far infrared and Raman spectra, the dielectric relaxation spectrum and its junction with the far infrared spectrum, are given. Conclusions are drawn concerning the structure of water and its modifications with temperature. They are compared to the theoretical previsions of the different models proposed for water [fr

  12. Water in Room Temperature Ionic Liquids

    Science.gov (United States)

    Fayer, Michael

    2014-03-01

    Room temperature ionic liquids (or RTILs, salts with a melting point below 25 °C) have become a subject of intense study over the last several decades. Currently, RTIL application research includes synthesis, batteries, solar cells, crystallization, drug delivery, and optics. RTILs are often composed of an inorganic anion paired with an asymmetric organic cation which contains one or more pendant alkyl chains. The asymmetry of the cation frustrates crystallization, causing the salt's melting point to drop significantly. In general, RTILs are very hygroscopic, and therefore, it is of interest to examine the influence of water on RTIL structure and dynamics. In addition, in contrast to normal aqueous salt solutions, which crystallize at low water concentration, in an RTIL it is possible to examine isolated water molecules interacting with ions but not with other water molecules. Here, optical heterodyne-detected optical Kerr effect (OHD-OKE) measurements of orientational relaxation on a series of 1-alkyl-3-methylimidazolium tetrafluoroborate RTILs as a function of chain length and water concentration are presented. The addition of water to the longer alkyl chain RTILs causes the emergence of a long time bi-exponential orientational anisotropy decay. Such decays have not been seen previously in OHD-OKE experiments on any type of liquid and are analyzed here using a wobbling-in-a-cone model. The orientational relaxation is not hydrodynamic, with the slowest relaxation component becoming slower as the viscosity decreases for the longest chain, highest water content samples. The dynamics of isolated D2O molecules in 1-butyl-3-methylimidazolium hexafluorophosphate (BmImPF6) were examined using two dimensional infrared (2D IR) vibrational echo spectroscopy. Spectral diffusion and incoherent and coherent transfer of excitation between the symmetric and antisymmetric modes are examined. The coherent transfer experiments are used to address the nature of inhomogeneous

  13. Modeling global persistent organic chemicals in clouds

    Science.gov (United States)

    Mao, Xiaoxuan; Gao, Hong; Huang, Tao; Zhang, Lisheng; Ma, Jianmin

    2014-10-01

    A cloud model was implemented in a global atmospheric transport model to simulate cloud liquid water content and quantify the influence of clouds on gas/aqueous phase partitioning of persistent organic chemicals (POCs). Partitioning fractions of gas/aqueous and particle phases in clouds for three POCs α-hexachlorocyclohexane (α-HCH), polychlorinated biphenyl-28 (PCB-28), and PCB-138 in a cloudy atmosphere were estimated. Results show that the partition fraction of these selected chemicals depend on cloud liquid water content (LWC) and air temperature. We calculated global distribution of water droplet/ice particle-air partitioning coefficients of the three chemicals in clouds. The partition fractions at selected model grids in the Northern Hemisphere show that α-HCH, a hydrophilic chemical, is sorbed strongly onto cloud water droplets. The computed partition fractions at four selected model grids show that α-HCH tends to be sorbed onto clouds over land (source region) from summer to early fall, and over ocean from late spring to early fall. 20-60% of α-HCH is able to be sorbed to cloud waters over mid-latitude oceans during summer days. PCB-138, one of hydrophobic POCs, on the other hand, tends to be sorbed to particles in the atmosphere subject to air temperature. We also show that, on seasonal or annual average, 10-20% of averaged PCB-28 over the Northern Hemisphere could be sorbed onto clouds, leading to reduction of its gas-phase concentration in the atmosphere.

  14. Autodissociation of a water molecule in liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Geissler, Phillip L.; Dellago, Christoph; Chandler, David; Hutter, Jurg; Parrinello, Michele

    2000-04-01

    The dissociation of a water molecule in liquid water is the fundamental event in acid-base chemistry, determining the pH of water.Because the microscopic dynamics of this autodissociation are difficult to probe, both by experiment and by computer simulation, its mechanism has been unknown. Here we report several autodissociation trajectories generated by ab initio molecular dynamics [1]. These trajectories, which were harvested using transition path sampling [2-4], reveal the mechanism for the first time. Rare fluctuations in solvation energies destabilize an oxygen-hydrogen bond. Through the transfer of one or more protons along a hydrogen bond.

  15. Metastable liquid-liquid transition in a molecular model of water.

    Science.gov (United States)

    Palmer, Jeremy C; Martelli, Fausto; Liu, Yang; Car, Roberto; Panagiotopoulos, Athanassios Z; Debenedetti, Pablo G

    2014-06-19

    Liquid water's isothermal compressibility and isobaric heat capacity, and the magnitude of its thermal expansion coefficient, increase sharply on cooling below the equilibrium freezing point. Many experimental, theoretical and computational studies have sought to understand the molecular origin and implications of this anomalous behaviour. Of the different theoretical scenarios put forward, one posits the existence of a first-order phase transition that involves two forms of liquid water and terminates at a critical point located at deeply supercooled conditions. Some experimental evidence is consistent with this hypothesis, but no definitive proof of a liquid-liquid transition in water has been obtained to date: rapid ice crystallization has so far prevented decisive measurements on deeply supercooled water, although this challenge has been overcome recently. Computer simulations are therefore crucial for exploring water's structure and behaviour in this regime, and have shown that some water models exhibit liquid-liquid transitions and others do not. However, recent work has argued that the liquid-liquid transition has been mistakenly interpreted, and is in fact a liquid-crystal transition in all atomistic models of water. Here we show, by studying the liquid-liquid transition in the ST2 model of water with the use of six advanced sampling methods to compute the free-energy surface, that two metastable liquid phases and a stable crystal phase exist at the same deeply supercooled thermodynamic condition, and that the transition between the two liquids satisfies the thermodynamic criteria of a first-order transition. We follow the rearrangement of water's coordination shell and topological ring structure along a thermodynamically reversible path from the low-density liquid to cubic ice. We also show that the system fluctuates freely between the two liquid phases rather than crystallizing. These findings provide unambiguous evidence for a liquid-liquid transition in

  16. (Liquid + liquid) equilibria of (water + ethanol + dimethyl glutarate) at several temperatures[(Liquid+liquid) equilibria; Ethanol; Dimethyl glutarate; UNIFAC method

    Energy Technology Data Exchange (ETDEWEB)

    Ince, Erol. E-mail: erolince@istanbul.edu.tr; Kirbaslar, S. Ismail. E-mail: krbaslar@istanbul.edu.tr

    2003-10-01

    (Liquid + liquid) equilibrium (LLE) data of (water + ethanol + dimethyl glutarate) have been determined experimentally at T=(298.15,308.15 and 318.15) K. The reliability of the experimental tie-line data was ascertained by using the Othmer and Tobias correlation. The LLE data of the ternary mixture were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  17. Polarized View of Supercooled Liquid Water Clouds

    Science.gov (United States)

    Alexandrov, Mikhail D.; Cairns, Brian; Van Diedenhoven, Bastiaan; Ackerman, Andrew S.; Wasilewski, Andrzej P.; McGill, Matthew J.; Yorks, John E.; Hlavka, Dennis L.; Platnick, Steven E.; Arnold, G. Thomas

    2016-01-01

    Supercooled liquid water (SLW) clouds, where liquid droplets exist at temperatures below 0 C present a well known aviation hazard through aircraft icing, in which SLW accretes on the airframe. SLW clouds are common over the Southern Ocean, and climate-induced changes in their occurrence is thought to constitute a strong cloud feedback on global climate. The two recent NASA field campaigns POlarimeter Definition EXperiment (PODEX, based in Palmdale, California, January-February 2013) and Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys (SEAC4RS, based in Houston, Texas in August- September 2013) provided a unique opportunity to observe SLW clouds from the high-altitude airborne platform of NASA's ER-2 aircraft. We present an analysis of measurements made by the Research Scanning Polarimeter (RSP) during these experiments accompanied by correlative retrievals from other sensors. The RSP measures both polarized and total reflectance in 9 spectral channels with wavelengths ranging from 410 to 2250 nm. It is a scanning sensor taking samples at 0.8deg intervals within 60deg from nadir in both forward and backward directions. This unique angular resolution allows for characterization of liquid water droplet size using the rainbow structure observed in the polarized reflectances in the scattering angle range between 135deg and 165deg. Simple parametric fitting algorithms applied to the polarized reflectance provide retrievals of the droplet effective radius and variance assuming a prescribed size distribution shape (gamma distribution). In addition to this, we use a non-parametric method, Rainbow Fourier Transform (RFT),which allows retrieval of the droplet size distribution without assuming a size distribution shape. We present an overview of the RSP campaign datasets available from the NASA GISS website, as well as two detailed examples of the retrievals. In these case studies we focus on cloud fields with spatial features

  18. Characteristics of bacterial community in cloud water at Mt Tai: similarity and disparity under polluted and non-polluted cloud episodes

    Science.gov (United States)

    Wei, Min; Xu, Caihong; Chen, Jianmin; Zhu, Chao; Li, Jiarong; Lv, Ganglin

    2017-04-01

    Bacteria are widely distributed in atmospheric aerosols and are indispensable components of clouds, playing an important role in the atmospheric hydrological cycle. However, limited information is available about the bacterial community structure and function, especially for the increasing air pollution in the North China Plain. Here, we present a comprehensive characterization of bacterial community composition, function, variation, and environmental influence for cloud water collected at Mt Tai from 24 July to 23 August 2014. Using Miseq 16S rRNA gene sequencing, the highly diverse bacterial community in cloud water and the predominant phyla of Proteobacteria, Bacteroidetes, Cyanobacteria, and Firmicutes were investigated. Bacteria that survive at low temperature, radiation, and poor nutrient conditions were found in cloud water, suggesting adaption to an extreme environment. The bacterial gene functions predicted from the 16S rRNA gene using the Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) suggested that the pathways related to metabolism and disease infections were significantly correlated with the predominant genera. The abundant genera Acinetobacter, Stenotrophomonas, Pseudomonas, and Empedobacter originated from a wide range of habitats including cloud condensation nuclei and ice nuclei active species, opportunistic pathogens, and functional species, demonstrating the importance of ecology and health in cloud water. Cluster analysis including hierarchical cluster (Hcluster) and principal coordinate analysis (PCoA) indicated a significant disparity between polluted and non-polluted samples. Linear discriminant analysis effect size (LEfSe) demonstrated that potential pathogens were enriched in the polluted cloud samples, whereas the diverse ecological function groups were significant in the non-polluted samples. Discrepant community structure determined by redundancy analysis (RDA) indicated that the major ions in

  19. Modeling water transport in liquid feed direct methanol fuel cells

    Science.gov (United States)

    Liu, Wenpeng; Wang, Chao-Yang

    Proper water management in direct methanol fuel cells (DMFCs) is very critical and complicated because of many interacting physicochemical phenomena. Among these, the liquid saturation in the cathode side is believed to have a very strong effect on water crossover through the membrane, a key parameter to determine water balance between the anode and cathode. In this paper, based on an interfacial liquid coverage model implemented in a three-dimensional (3D) two-phase DMFC model, the liquid saturation variations in the cathode are examined in detail and their effects on the net water transport coefficient through the membrane discussed.

  20. Preliminary experimental study of liquid lithium water interaction

    Energy Technology Data Exchange (ETDEWEB)

    You, X.M.; Tong, L.L.; Cao, X.W., E-mail: caoxuewu@sjtu.edu.cn

    2015-10-15

    Highlights: • Explosive reaction occurs when lithium temperature is over 300 °C. • The violence of liquid lithium water interaction increases with the initial temperature of liquid lithium. • The interaction is suppressed when the initial water temperature is above 70 °C. • Steam explosion is not ignorable in the risk assessment of liquid lithium water interaction. • Explosion strength of liquid lithium water interaction is evaluated by explosive yield. - Abstract: Liquid lithium is the best candidate for a material with low Z and low activation, and is one of the important choices for plasma facing materials in magnetic fusion devices. However, liquid lithium reacts violently with water under the conditions of loss of coolant accidents. The release of large heats and hydrogen could result in the dramatic increase of temperature and pressure. The lithium–water explosion has large effect on the safety of fusion devices, which is an important content for the safety assessment of fusion devices. As a preliminary investigation of liquid lithium water interaction, the test facility has been built and experiments have been conducted under different conditions. The initial temperature of lithium droplet ranged from 200 °C to 600 °C and water temperature was varied between 20 °C and 90 °C. Lithium droplets were released into the test section with excess water. The shape of lithium droplet and steam generated around the lithium were observed by the high speed camera. At the same time, the pressure and temperature in the test section were recorded during the violent interactions. The preliminary experimental results indicate that the initial temperature of lithium and water has an effect on the violence of liquid lithium water interaction.

  1. Observed reflectivities and liquid water content for marine stratocumulus

    Science.gov (United States)

    Coakley, J. A., Jr.; Snider, J. B.

    1989-01-01

    Simultaneous observations of cloud liquid water content and cloud reflectivity are used to verify their parametric relationship in a manner consistent with simple parameterizations often used in general-circulation climate models. The column amount of cloud liquid water was measured with a microwave radiometer on San Nicolas Island as described by Hogg et al., (1983). Cloud reflectivity was obtained through spatial coherence analysis of AVHRR imagery data as per Coakley and Baldwin (1984) and Coakley and Beckner (1988). The dependence of the observed reflectivity on the observed liquid water is discussed, and this empirical relationship is compared with the parameterization proposed by Stephens (1978).

  2. High frequency, realtime measurements of stable isotopes in liquid water

    Science.gov (United States)

    Weiler, M.; Herbstritt, B.; Gralher, B.

    2012-04-01

    We developed a method to measure in-situ the isotopic composition of liquid water with minimal supervision and, most important, with a temporal resolution of less than a minute. For this purpose a off-the-shelf microporous hydrophobic membrane contactor for under 200€ was combined with an isotope laser spectrometer (Picarro). The contactor, originally designed for degassing liquids, was used with nitrogen as carrier gas in order to transform a small fraction of liquid water to water vapor. The generated water vapor was then analyzed continuously by the isotope laser spectrometer. To prove the membrane's applicability we determined the specific isotope fractionation factor for the phase change through the contactor's membrane for a common temperature range and with different waters of known isotopic compositions. This fractionation factor is then used to derive the liquid water isotope ratio from the measured water vapor isotope ratios and the measured temperature at the phase change. The system was compared for breakthrough curves of isotopically enriched water and the isotope values corresponded very well with those of liquid water samples taken simultaneously and analyzed with a conventional method (CRDS). The introduced method supersedes taking liquid samples and employs only relative cheap and readily available components. This makes it a relatively inexpensive, fast, user-friendly and easily reproducible method. It can be applied in both the field and laboratory wherever a water vapor isotope analyzer can be run and whenever real-time isotope data of liquid water are required at high temporal resolution with the same accuracy as collecting individual water samples.

  3. Further evidence of a liquid-liquid transition in interfacial water

    International Nuclear Information System (INIS)

    Zanotti, J-M; Bellissent-Funel, M C; Chen, S-H; Kolesnikov, A I

    2006-01-01

    In a previous paper we combined calorimetric, diffraction and high-resolution quasi-elastic neutron scattering data to show that after exhibiting a glass transition at 165 K, interfacial water experiences a first order liquid-liquid transition at 240 K from a low-density to a high-density liquid. Here we present further evidence of these transitions obtained by high-energy inelastic neutron scattering

  4. (Liquid + liquid) equilibria of (water + propionic acid + cyclohexanone) at several temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Cehreli, Sueheyla [Istanbul University, Engineering Faculty, Department of Chemical Engineering, 34320 Istanbul (Turkey)]. E-mail: cehreli@istanbul.edu.tr; Tatli, Besir [Istanbul University, Engineering Faculty, Department of Chemical Engineering, 34320 Istanbul (Turkey); Bagman, Pelin [Istanbul University, Engineering Faculty, Department of Chemical Engineering, 34320 Istanbul (Turkey)

    2005-12-15

    (Liquid + liquid) equilibrium (LLE) data for (water + propionic acid + cyclohexanone) were measured under atmospheric pressure and at T = (293.2, 298.2 and 303.2) K. Phase diagrams were obtained by determining solubility and tie-line data. The LLE data of the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated over the immiscibility regions.

  5. Liquid water in the domain of cubic crystalline ice Ic.

    Science.gov (United States)

    Jenniskens, P; Banham, S F; Blake, D F; McCoustra, M R

    1997-07-22

    Vapor-deposited amorphous water ice when warmed above the glass transition temperature (120-140 K), is a viscous liquid which exhibits a viscosity vs temperature relationship different from that of liquid water at room temperature. New studies of thin water ice films now demonstrate that viscous liquid water persists in the temperature range 140-210 K. where it coexists with cubic crystalline ice. The liquid character of amorphous water above the glass transition is demonstrated by (1) changes in the morphology of water ice films on a nonwetting surface observed in transmission electron microscopy (TEM) at around 175 K during slow warming, (2) changes in the binding energy of water molecules measured in temperature programmed desorption (TPD) studies, and (3) changes in the shape of the 3.07 micrometers absorption band observed in grazing angle reflection-absorption infrared spectroscopy (RAIRS) during annealing at high temperature. whereby the decreased roughness of the water surface is thought to cause changes in the selection rules for the excitation of O-H stretch vibrations. Because it is present over such a wide range of temperatures, we propose that this form of liquid water is a common material in nature. where it is expected to exist in the subsurface layers of comets and on the surfaces of some planets and satellites.

  6. Droplet-Sizing Liquid Water Content Sensor Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Icing is one of the most significant hazards to aircraft. A sizing supercooled liquid water content (SSLWC) sonde is being developed to meet a directly related need...

  7. Droplet-Sizing Liquid Water Content Sensor, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — Icing is one of the most significant hazards to aircraft. A sizing supercooled liquid water content (SSLWC) sonde is being developed to meet a directly related need...

  8. Continuous in situ measurements of stable isotopes in liquid water

    Science.gov (United States)

    Herbstritt, Barbara; Gralher, Benjamin; Weiler, Markus

    2012-03-01

    We developed a method to measure in situ the isotopic composition of liquid water with minimal supervision and, most important, with a temporal resolution of less than a minute. For this purpose a microporous hydrophobic membrane contactor (Membrana) was combined with an isotope laser spectrometer (Picarro). The contactor, originally designed for degassing liquids, was used with N2 as a carrier gas in order to transform a small fraction of liquid water to water vapor. The generated water vapor was then analyzed continuously by the Picarro analyzer. To prove the membrane's applicability, we determined the specific isotope fractionation factor for the phase change through the contactor's membrane across an extended temperature range (8°C-21°C) and with different waters of known isotopic compositions. This fractionation factor is needed to subsequently derive the liquid water isotope ratio from the measured water vapor isotope ratios. The system was tested with a soil column experiment, where the isotope values derived with the new method corresponded well (R2 = 0.998 for δ18O and R2 = 0.997 for δ2H) with those of liquid water samples taken simultaneously and analyzed with a conventional method (cavity ring-down spectroscopy). The new method supersedes taking liquid samples and employs only relatively cheap and readily available components. This makes it a relatively inexpensive, fast, user-friendly, and easily reproducible method. It can be applied in both the field and laboratory wherever a water vapor isotope analyzer can be run and whenever real-time isotope data of liquid water are required at high temporal resolution.

  9. Liquid nitrogen - water interaction experiments for fusion reactor accident scenarios

    International Nuclear Information System (INIS)

    Duckworth, R.; Murphy, J.; Pfotenhauer, J.; Corradini, M.

    2001-01-01

    With the implementation of superconducting magnets in fusion reactors, the possibility exists for the interaction between water and cryogenic systems. The interaction between liquid nitrogen and water was investigated experimentally and numerically. The rate of pressurization and peak pressure were found to be driven thermodynamically by the expansion of the water and the boil-off of the liquid nitrogen and did not have a vapor explosion nature. Since the peak pressure was small in comparison to previous work with stratified geometries, the role of the geometry of the interacting fluids has been shown to be significant. Comparisons of the peak pressure and the rate of pressurization with respect to the ratio of the liquid nitrogen mass to water mass reveal no functional dependence as was observed in the liquid helium-water experiments. A simple thermodynamic model provides a fairly good description of the pressure rise data. From the data, the model will allow one to extract the interaction area of the water. As with previous liquid helium-water interaction experiments, more extensive investigation of the mass ratio and interaction geometry is needed to define boundaries between explosive and non-explosive conditions. (authors)

  10. Liquid Water in the Extremely Shallow Martian Subsurface

    Science.gov (United States)

    Pavlov, A.; Shivak, J. N.

    2012-01-01

    Availability of liquid water is one of the major constraints for the potential Martian biosphere. Although liquid water is unstable on the surface of Mars due to low atmospheric pressures, it has been suggested that liquid films of water could be present in the Martian soil. Here we explored a possibility of the liquid water formation in the extremely shallow (1-3 cm) subsurface layer under low atmospheric pressures (0.1-10 mbar) and low ("Martian") surface temperatures (approx.-50 C-0 C). We used a new Goddard Martian simulation chamber to demonstrate that even in the clean frozen soil with temperatures as low as -25C the amount of mobile water can reach several percents. We also showed that during brief periods of simulated daylight warming the shallow subsurface ice sublimates, the water vapor diffuses through porous surface layer of soil temporarily producing supersaturated conditions in the soil, which leads to the formation of additional liquid water. Our results suggest that despite cold temperatures and low atmospheric pressures, Martian soil just several cm below the surface can be habitable.

  11. Review: Drinking water for liquid-fed pigs.

    Science.gov (United States)

    Meunier-Salaün, M-C; Chiron, J; Etore, F; Fabre, A; Laval, A; Pol, F; Prunier, A; Ramonet, Y; Nielsen, B L

    2017-05-01

    Liquid feeding has the potential to provide pigs with sufficient water to remain hydrated and prevent prolonged thirst. However, lack of permanent access to fresh water prevents animals from drinking when they are thirsty. Moreover, individual differences between pigs in a pen may result in uneven distribution of the water provided by the liquid feed, leading to some pigs being unable to meet their water requirements. In this review, we look at the need for and provision of water for liquid-fed pigs in terms of their production performance, behaviour, health and welfare. We highlight factors which may lead to water ingestion above or below requirements. Increases in the need for water may be caused by numerous factors such as morbidity, ambient temperature or competition within the social group, emphasising the necessity of permanent access to water as also prescribed in EU legislation. The drinkers can be the target of redirected behaviour in response to feed restriction or in the absence of rooting materials, thereby generating water losses. The method of water provision and drinker design is critical to ensure easy access to water regardless of the pig's physiological state, and to limit the amount of water used, which does not benefit the pig.

  12. Anharmonic bend-stretch coupling in neat liquid water

    NARCIS (Netherlands)

    Lindner, Joerg; Cringus, Dan; Pshenichnikov, Maxim S.; Voehringer, Peter

    2007-01-01

    Femtosecond mid-IR spectroscopy is used to study the vibrational relaxation dynamics in neat liquid water. By exciting the bending vibration and probing the stretching mode, it is possible to reliably determine the bending and librational lifetimes of water. The anharmonic coupling between the

  13. (Liquid + liquid) equilibrium of {water + phenol + (1-butanol, or 2-butanol, or tert-butanol)} systems

    International Nuclear Information System (INIS)

    Hadlich de Oliveira, Leonardo; Aznar, Martin

    2010-01-01

    (Liquid + liquid) equilibrium (LLE) and binodal curve data were determined for the systems (water + phenol + tert-butanol) at T = 298.15 K, (water + phenol + 2-butanol) and (water + phenol + 1-butanol) at T = 298.15 K and T = 313.15 K by the combined techniques of densimetry and refractometry. Type I curve (for tert-butanol) and Type II curves (for 1- and 2-butanol) were found. The data were correlated with the NRTL model and the parameters estimated present root mean square deviations below 2% for the system with tert-butanol and lower than 0.8% for the other systems.

  14. The puzzling unsolved mysteries of liquid water: Some recent progress

    Science.gov (United States)

    Stanley, H. E.; Kumar, P.; Xu, L.; Yan, Z.; Mazza, M. G.; Buldyrev, S. V.; Chen, S.-H.; Mallamace, F.

    2007-12-01

    Water is perhaps the most ubiquitous, and the most essential, of any molecule on earth. Indeed, it defies the imagination of even the most creative science fiction writer to picture what life would be like without water. Despite decades of research, however, water's puzzling properties are not understood and 63 anomalies that distinguish water from other liquids remain unsolved. We introduce some of these unsolved mysteries, and demonstrate recent progress in solving them. We present evidence from experiments and computer simulations supporting the hypothesis that water displays a special transition point (which is not unlike the “tipping point” immortalized by Malcolm Gladwell). The general idea is that when the liquid is near this “tipping point,” it suddenly separates into two distinct liquid phases. This concept of a new critical point is finding application to other liquids as well as water, such as silicon and silica. We also discuss related puzzles, such as the mysterious behavior of water near a protein.

  15. Surface potential of the water liquid-vapor interface

    Science.gov (United States)

    Wilson, Michael A.; Pohorille, Andrew; Pratt, Lawrence R.

    1988-01-01

    An analysis of an extended molecular dynamics calculation of the surface potential (SP) of the water liquid-vapor interface is presented. The SP predicted by the TIP4P model is -(130 + or - 50) mV. This value is of reasonable magnitude but of opposite sign to the expectations based on laboratory experiments. The electrostatic potential shows a nonmonotonic variation with depth into the liquid.

  16. Structure of liquid water at high pressures and temperatures

    International Nuclear Information System (INIS)

    Eggert, Jon H; Weck, Gunnar; Loubeyre, Paul

    2002-01-01

    We report quantitatively accurate structure-factor and radial-distribution-function measurements of liquid water in a diamond-anvil cell (DAC) using x-ray diffraction. During the analysis of our diffraction data, we found it possible (and necessary) to also determine the density. Thus, we believe we present the first-ever diffraction-based determination of a liquid structure factor and equation of state in a DAC experiment

  17. (Liquid + liquid) equilibria of (water + propionic acid + dimethyl phthalate) at several temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Oezmen, Dilek [Engineering Faculty, Department of Chemical Engineering, Istanbul University, 34320 Istanbul (Turkey); Cehreli, Sueheyla [Engineering Faculty, Department of Chemical Engineering, Istanbul University, 34320 Istanbul (Turkey)]. E-mail: cehreli@istanbul.edu.tr; Dramur, Umur [Engineering Faculty, Department of Chemical Engineering, Istanbul University, 34320 Istanbul (Turkey)

    2005-08-15

    (Liquid + liquid) equilibrium (LLE) data for (water + propionic acid + dimethyl phthalate) were measured under atmospheric pressure and at T (298.2, 303.2, 308.2 and 313.2) K. Phase diagrams were obtained by determining solubility and tie-line data. The LLE data of the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated over the immiscibility regions.

  18. Core-softened fluids, water-like anomalies, and the liquid-liquid critical points.

    Science.gov (United States)

    Salcedo, Evy; de Oliveira, Alan Barros; Barraz, Ney M; Chakravarty, Charusita; Barbosa, Marcia C

    2011-07-28

    Molecular dynamics simulations are used to examine the relationship between water-like anomalies and the liquid-liquid critical point in a family of model fluids with multi-Gaussian, core-softened pair interactions. The core-softened pair interactions have two length scales, such that the longer length scale associated with a shallow, attractive well is kept constant while the shorter length scale associated with the repulsive shoulder is varied from an inflection point to a minimum of progressively increasing depth. The maximum depth of the shoulder well is chosen so that the resulting potential reproduces the oxygen-oxygen radial distribution function of the ST4 model of water. As the shoulder well depth increases, the pressure required to form the high density liquid decreases and the temperature up to which the high-density liquid is stable increases, resulting in the shift of the liquid-liquid critical point to much lower pressures and higher temperatures. To understand the entropic effects associated with the changes in the interaction potential, the pair correlation entropy is computed to show that the excess entropy anomaly diminishes when the shoulder well depth increases. Excess entropy scaling of diffusivity in this class of fluids is demonstrated, showing that decreasing strength of the excess entropy anomaly with increasing shoulder depth results in the progressive loss of water-like thermodynamic, structural and transport anomalies. Instantaneous normal mode analysis was used to index the overall curvature distribution of the fluid and the fraction of imaginary frequency modes was shown to correlate well with the anomalous behavior of the diffusivity and the pair correlation entropy. The results suggest in the case of core-softened potentials, in addition to the presence of two length scales, energetic, and entropic effects associated with local minima and curvatures of the pair interaction play an important role in determining the presence of water

  19. Structural Origin of Shear Viscosity of Liquid Water.

    Science.gov (United States)

    Yamaguchi, Tsuyoshi

    2018-01-25

    The relation between the microscopic structure and shear viscosity of liquid water was analyzed by calculating the cross-correlation between the shear stress and the two-body density using the molecular dynamics simulation. The slow viscoelastic relaxation that dominates the steady-state shear viscosity was ascribed to the destruction of the hydrogen-bonding network structure along the compression axis of the shear distortion, which resembles the structural change under isotropic hydrostatic compression. It means that the shear viscosity of liquid water reflects the anisotropic destruction-formation dynamics of the hydrogen-bonding network.

  20. Liquid velocity in upward and downward air-water flows

    International Nuclear Information System (INIS)

    Sun Xiaodong; Paranjape, Sidharth; Kim, Seungjin; Ozar, Basar; Ishii, Mamoru

    2004-01-01

    Local characteristics of the liquid phase in upward and downward air-water two-phase flows were experimentally investigated in a 50.8-mm inner-diameter round pipe. An integral laser Doppler anemometry (LDA) system was used to measure the axial liquid velocity and its fluctuations. No effect of the flow direction on the liquid velocity radial profile was observed in single-phase liquid benchmark experiments. Local multi-sensor conductivity probes were used to measure the radial profiles of the bubble velocity and the void fraction. The measurement results in the upward and downward two-phase flows are compared and discussed. The results in the downward flow demonstrated that the presence of the bubbles tended to flatten the liquid velocity radial profile, and the maximum liquid velocity could occur off the pipe centerline, in particular at relatively low flow rates. However, the maximum liquid velocity always occurred at the pipe center in the upward flow. Also, noticeable turbulence enhancement due to the bubbles in the two-phase flows was observed in the current experimental flow conditions. Furthermore, the distribution parameter and the void-weighted area-averaged drift velocity were obtained based on the definitions

  1. Liquid-Liquid equilibria of the water-acetic acid-butyl acetate system

    Directory of Open Access Journals (Sweden)

    Ince E.

    2002-01-01

    Full Text Available Experimental liquid-liquid equilibria of the water-acetic acid-butyl acetate system were studied at temperatures of 298.15± 0.20, 303.15± 0.20 and 308.15± 0.20 K. Complete phase diagrams were obtained by determining solubility and tie-line data. The reliability of the experimental tie-line data was ascertained by using the Othmer and Tobias correlation. The UNIFAC group contribution method was used to predict the observed ternary liquid-liquid equilibrium (LLE data. It was found that UNIFAC group interaction parameters used for LLE did not provide a good prediction. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  2. Limiting shear stress and monotonic properties of liquid water

    Science.gov (United States)

    Gorshkov, A. I.

    2016-12-01

    Publications in scientific journals in which the authors attempt to experimentally prove that water, the most widespread substance on the Earth, is not a completely classical liquid, have become more frequent recently. This means, first, that water behaves as a solid at very low shear stress, i.e., does not flow, and, second, that the temperature dependences of its different properties are non-monotonic, i.e., possess singularities. We are aware of several such publications [1-5].

  3. Water Phase Diagram Is Significantly Altered by Imidazolium Ionic Liquid

    DEFF Research Database (Denmark)

    Chaban, V. V.; Prezhdo, O. V.

    2014-01-01

    of water, as represented, for instance, by strong negative deviations from Raoult's law, extending far beyond the standard descriptions. The investigation was carried out using classical molecular dynamics employing a specifically refined force field. The changes in the liquid-vapor interface and saturated...

  4. A fate for organic acids, formaldehyde and methanol in cloud water: their biotransformation by micro-organisms

    OpenAIRE

    Amato, Pierre; Demeer, F.; Melaouhi, A.; Fontanella, Stéphane; Martin-Biesse, A.-S.; Sancelme, M.; Laj, Paolo; Delort, A.M.

    2007-01-01

    The interactions between microbial and chemical contents of cloud water were investigated. First, we observe that the bulk cloud water solution provides a substantial environment where bacteria can develop significantly. Then, a total number of 60 microbial strains originating from seven distinct samples of cloud water and affiliated to various taxonomic groups were examined for their ability to degrade some of the main atmospheric carboxylic compounds: formate, acetate, lactate, succinate, a...

  5. APPLICATION OF THE UNIFAC MODEL TO LIQUID-LIQUID EQUILIBRIA OF WATER-PROPIONIC ACID-SOLVENT TERNARIES*

    Directory of Open Access Journals (Sweden)

    Süheyla ÇEHRELİ

    2003-01-01

    Full Text Available The liquid-liquid equilibria of Water-Propionic Acid-Benzyl Alcohol, Water-Propionic Acid-Benzyl Acetate and Water-Propionic Acid-Dibenzyl Ether ternary systems were predicted by means of UNIFAC Model. For this purpose, multivariable Newton-Raphson convergence procedure was used. Experimental and model results were compared.

  6. Neutron diffraction study of the structure of liquid water

    International Nuclear Information System (INIS)

    Ohtomo, Norio; Arakawa, Kiyoshi.

    1978-01-01

    The structure factor for heavy water at 17 0 C up to the Q value of 18 A -1 has been determined by means of the time-of-flight (TOF) diffraction method using pulsed neutrons produced by LINAC. The result has been compared with structure factors calculated on the basis of the various structure models of liquid water; the ''uncorrelated orientation model'' and the ''watery model'' (Page and Powles), the ''near-neighbor model'' (Narten) and the ''revised watery model'' (authors). None of these models has been found to fit the neutron diffraction data satisfactorily over the entire range of Q, though our curve is somewhat improved in comparison with the curves for earlier models. Some discussions about the various structure models of liquid water have been made. (auth.)

  7. Recommended Liquid-Liquid Equilibrium Data. Part 5. Ether-Water Systems

    Science.gov (United States)

    Góral, Marian; Måczyński, Andrzej; Oracz, Paweł

    2007-12-01

    Recommended liquid-liquid equilibrium (LLE) data for 12 binary ether-water systems have been obtained after the critical evaluation of all data (168 data sets) reported for 17 systems in the open literature up to the end of 2006. An equation for the prediction of the ether solubilities in water was developed. The predicted ether solubilities were used for the calculation of water solubility in the ether-rich phase. The LLE calculations were done with the equation of state appended with a chemical term (EoSC) proposed by Góral [Fluid Phase Equilib. 118, 27 (1996)]. The recommended data are presented in the form of individual tables with references. Using these recommended data, predictive ability has been tested for several UNIFAC and ASOG group-contribution methods.

  8. Measurement of liquid-liquid equilibria for condensate + glycol and condensate + glycol + water systems

    DEFF Research Database (Denmark)

    Riaz, Muhammad; Kontogeorgis, Georgios; Stenby, Erling Halfdan

    2011-01-01

    . The ultimate objective of this work is to develop a predictive thermodynamic model for the mutual solubility of oil, water, and polar chemicals. But for the development and validation of the model, experimental data are required. This work presents new experimental liquid-liquid equilibrium (LLE) data for 1...... into boiling range groups from hexane to nonane. Paraffinic (P), naphthenic (N), and aromatic (A) distributions were obtained for the boiling point fractions up to nonane. The average molar mass and the overall density of the condensate were measured experimentally. For the mutual solubility of MEG...

  9. (Liquid + liquid) equilibria of the (water + acetic acid + dibutyl phthalate) system

    Energy Technology Data Exchange (ETDEWEB)

    Kirbaslar, S. ismail [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)]. E-mail: krbaslar@istanbul.edu.tr; Ince, Erol [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)]. E-mail: erolince@istanbul.edu.tr; Yueksel, Sema [Mak-Plast, Mahmutbey Tasocagi Yolu, No. 7, 34560 Bagcilar, Istanbul (Turkey)

    2005-11-15

    (Liquid + liquid) equilibrium (LLE) data of the (water + acetic acid + dibutyl phthalate) system have been determined experimentally at T = (298.2, 308.2, and 318.2) K. The reliability of the experimental tie lines data was ascertained by using the Othmer-Tobias correlation. The UNIFAC model was used to predict the phase equilibrium in the system using the interaction parameters between AC, ACH, CH{sub 2}, CH{sub 3}, CH{sub 2}COO, COOH, and H{sub 2}O functional groups. The experimental data were compared with predicted by UNIFAC model. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  10. (Liquid + liquid) equilibria of the (water + butyric acid + dodecanol) ternary system

    Energy Technology Data Exchange (ETDEWEB)

    Kirbaslar, S. Ismail [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)]. E-mail: krbaslar@istanbul.edu.tr

    2006-06-15

    (Liquid + liquid) equilibrium (LLE) data for the (water + butyric acid + dodecanol) ternary system have been determined experimentally at T = (298.2, 308.2 and 318.2) K. Complete phase diagrams were obtained by determining binodal curves and tie lines. The reliability of the experimental tie lines was confirmed by using the Othmer-Tobias correlation. The UNIFAC method was used to predict the phase equilibrium in the ternary system using the interaction parameters determined from experimental data of CH{sub 3}, CH{sub 2}, COOH, OH and H{sub 2}O functional groups. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  11. (Liquid + liquid) equilibria of (water + propionic acid + diethyl phthalate) at several temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Cehreli, Sueheyla [Istanbul University, Engineering Faculty, Department of Chemical Engineering, 34320 Istanbul (Turkey)]. E-mail: cehreli@istanbul.edu.tr; Oezmen, Dilek [Istanbul University, Engineering Faculty, Department of Chemical Engineering, 34320 Istanbul (Turkey)]. E-mail: dilekus@istanbul.edu.tr; Tatli, Besir [Istanbul University, Engineering Faculty, Department of Chemical Engineering, 34320 Istanbul (Turkey)

    2005-10-15

    (Liquid + liquid) equilibrium (LLE) data for (water + propionic acid + diethyl phthalate) were measured under atmospheric pressure and at T (298.2, 303.2, 308.2, and 313.2) K. Phase diagrams were obtained by determining solubility and tie-line data. The UNIFAC model was used to correlate the experimental tie-line data. The average root-mean-square deviation between the observed and calculated mass fraction was 0.03. Distribution coefficients and separation factors were evaluated over the immiscibility regions.

  12. (Liquid + liquid) equilibrium of (dibutyl ether + methanol + water) at different temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Arce, Alberto [Department of Chemical Engineering, University of Santiago de Compostela, E-15782, Santiago de Compostela (Spain)]. E-mail: eqaaarce@usc.es; Rodriguez, Hector [Department of Chemical Engineering, University of Santiago de Compostela, E-15782, Santiago de Compostela (Spain); Rodriguez, Oscar [Department of Chemical Engineering, University of Santiago de Compostela, E-15782, Santiago de Compostela (Spain); Soto, Ana [Department of Chemical Engineering, University of Santiago de Compostela, E-15782, Santiago de Compostela (Spain)

    2005-09-15

    (Liquid + liquid) equilibrium data for the ternary system (dibutyl ether + methanol + water) were experimentally determined at T = (298.15, 308.15, and 318.15) K. The experimental results were correlated by means of the NRTL and UNIQUAC equations, the best results being achieved with the UNIQUAC equation, both for the individual correlations at each temperature and for the overall correlation considering all the three experimental data sets. The experimental tie-lines were also compared to the values predicted by the UNIFAC method.

  13. Liquid - liquid equilibria of the water + butyric acid + decanol ternary system

    Directory of Open Access Journals (Sweden)

    S.I. Kirbaslar

    2006-09-01

    Full Text Available Liquid-liquid equilibrium (LLE data for the water + butyric acid + decanol ternary system were determined experimentally at temperatures of 298.15, 308.15 and 318.15 K. Complete phase diagrams were obtained by determining the solubility curve and the tie lines. The reliability of the experimental tie line data was confirmed with the Othmer-Tobias correlation. The UNIFAC method was used to predict the phase equilibrium of the system using the interaction parameters for groups CH3, CH2, COOH, OH and H2O determined experimentally. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  14. (Liquid + liquid) equilibrium of (dibutyl ether + methanol + water) at different temperatures

    International Nuclear Information System (INIS)

    Arce, Alberto; Rodriguez, Hector; Rodriguez, Oscar; Soto, Ana

    2005-01-01

    (Liquid + liquid) equilibrium data for the ternary system (dibutyl ether + methanol + water) were experimentally determined at T = (298.15, 308.15, and 318.15) K. The experimental results were correlated by means of the NRTL and UNIQUAC equations, the best results being achieved with the UNIQUAC equation, both for the individual correlations at each temperature and for the overall correlation considering all the three experimental data sets. The experimental tie-lines were also compared to the values predicted by the UNIFAC method

  15. A liquid-liquid distribution method for the study of complexation of cadmium in natural waters

    International Nuclear Information System (INIS)

    Stary, J.; Kratzer, K.

    1990-01-01

    Liquid-liquid distribution of cadmium between pyridine solution in benzene and aqueous phase containing iodide was radiometrically investigated, in order to develop a simple method for the study of complexation of cadmium in aqueous solutions. The degree of complexation can be determined from the decrease of the distribution ratio in the presence of complexing agents forming non-extractable complexes with cadmium. The method was verified for the determination of the composition and stability constants of cadmium with acetate, tartrate, oxalate and glycolate anions and applied for the study of complexation of cadmium in natural waters. (author) 9 refs.; 4 figs

  16. Magnetic properties and core electron binding energies of liquid water

    Science.gov (United States)

    Galamba, N.; Cabral, Benedito J. C.

    2018-01-01

    The magnetic properties and the core and inner valence electron binding energies of liquid water are investigated. The adopted methodology relies on the combination of molecular dynamics and electronic structure calculations. Born-Oppenheimer molecular dynamics with the Becke and Lee-Yang-Parr functionals for exchange and correlation, respectively, and includes an empirical correction (BLYP-D3) functional and classical molecular dynamics with the TIP4P/2005-F model were carried out. The Keal-Tozer functional was applied for predicting magnetic shielding and spin-spin coupling constants. Core and inner valence electron binding energies in liquid water were calculated with symmetry adapted cluster-configuration interaction. The relationship between the magnetic shielding constant σ(17O), the role played by the oxygen atom as a proton acceptor and donor, and the tetrahedral organisation of liquid water are investigated. The results indicate that the deshielding of the oxygen atom in water is very dependent on the order parameter (q) describing the tetrahedral organisation of the hydrogen bond network. The strong sensitivity of magnetic properties on changes of the electronic density in the nuclei environment is illustrated by a correlation between σ(17O) and the energy gap between the 1a1[O1s] (core) and the 2a1 (inner valence) orbitals of water. Although several studies discussed the eventual connection between magnetic properties and core electron binding energies, such a correlation could not be clearly established. Here, we demonstrate that for liquid water this correlation exists although involving the gap between electron binding energies of core and inner valence orbitals.

  17. The liquid water balance of the Greenland ice sheet

    Science.gov (United States)

    Steger, Christian; Reijmer, Carleen; van den Broeke, Michiel

    2017-04-01

    Mass loss from the Greenland Ice Sheet (GrIS) is an increasingly important contributor to global sea level rise. During the last decade, the mass loss was dominated by meltwater runoff. Linking actual runoff from the ice sheet to melt and other forms of liquid water input at the surface (rainfall and condensation) is however complex, as liquid water may be retained within the ice sheet due to refreezing and/or (perennial) storage. In the ablation zone on bare ice, liquid water runs of laterally at the surface, accumulates in supraglacial lakes or enters the ice sheet's en- or subglacial hydraulic system via moulins and crevasses. In the higher elevated accumulation zone, liquid water percolates into the porous firn layer and part of it may be retained due to refreezing and/or perennial storage in so called firn aquifers. In this study, we investigate the liquid water balance of the GrIS focussing on the role of the firn layer. For this purpose, we ran SNOWPACK, a relatively complex one-dimensional snow model, on a horizontal resolution of ˜ 11km and for the transient period of 1960 to 2015. At the snow-atmosphere-interface, the model was forced by output of the regional atmospheric climate model RACMO2.3. A comparison of SNOWPACK with in-situ observations (firn density profiles) and remote sensing data (firn aquifer locations inferred from radar measurements) indicated a good agreement for most climatic conditions. On a GrIS-wide scale, the modelled surface mass balance of SNOWPACK exhibits, in combination with ice-discharge data for ocean-terminating glaciers, an excellent agreement with GRACE data for the period 2003 - 2012. GrIS-integrated amounts of surface melt reveal a significant positive trend (+11.6Gta-2) in the second half of the simulation period. Within this interval, the trend in runoff is larger (+8.3Gta-2) than the one in refreezing (+3.6Gta-2), which results in an overall decrease of the refreezing fraction. This decrease is for instance less

  18. Liquid radioactive waste processing system for pressurized water reactor plants

    International Nuclear Information System (INIS)

    Anon.

    1976-01-01

    This Standard sets forth design, construction, and performance requirements, with due consideration for operation, of the Liquid Radioactive Waste Processing System for pressurized water reactor plants for design basis inputs. For the purpose of this Standard, the Liquid Radioactive Waste Processing System begins at the interfaces with the reactor coolant pressure boundary and the interface valve(s) in lines from other systems, or at those sumps and floor drains provided for liquid waste with the potential of containing radioactive material; and it terminates at the point of controlled discharge to the environment, at the point of interface with the waste solidification system, and at the point of recycle back to storage for reuse

  19. Effect of ionic liquid 1-methylimidazolium chloride on the vapour liquid equilibrium of water, methanol, ethanol, and {water + ethanol} mixture

    International Nuclear Information System (INIS)

    Shen Chong; Li Xuemei; Lu Yingzhou; Li Chunxi

    2011-01-01

    Highlights: → Vapour pressure data for three binary systems and a ternary system were measured. → Water, ethanol, methanol, and 1-methylimidazolium chloride were studied. → The vapour pressure data can be well correlated by the NRTL model. → The isobaric (vapour + liquid) equilibria were predicted by the NRTL model. → The salt effect of ILs on the VLE of {water + ethanol} mixture was investigated. - Abstract: Measurements of vapour pressure data were conducted using a quasi-static ebulliometer for systems containing water, methanol, ethanol, and a mixture of {water + ethanol} in the presence of an ionic liquid (IL), namely, 1-methylimidazolium chloride ([MIm]Cl), wherein the IL-content ranged from w 2 = (0.10 to 0.50). The vapour pressure data of IL-containing binary systems were correlated by the NRTL model with an overall average absolute relative deviation (AARD) of 0.0103, and the resulting binary parameters were used to predict the vapour pressures of a ternary system {water + ethanol + [MIm]Cl} with an AARD less than 0.0077. Further, the isobaric vapour liquid equilibria (VLE) for the ternary system {water + ethanol + IL} with IL-content of w 3 = (0.10, 0.30, and 0.50) for [MIm]Cl and x 3 = 0.15 for [MIm]Cl, [C 4 MIm]Cl, and [C 6 MIm]Cl were predicted at 101.3 kPa, respectively. It is indicated that [MIm]Cl presents the strongest ability to enhance the relative volatility of ethanol to water in the mixture of {water + ethanol} than that of [C 4 MIm]Cl and [C 6 MIm]Cl, which is consistent with the cationic sizes and hence the ionic hydration ability. Therefore, distillation separation of the azeotrope of {water + ethanol} can be sufficiently facilitated by the addition of [MIm]Cl at a specified content.

  20. Liquid-liquid critical point in a simple analytical model of water

    Science.gov (United States)

    Urbic, Tomaz

    2016-10-01

    A statistical model for a simple three-dimensional Mercedes-Benz model of water was used to study phase diagrams. This model on a simple level describes the thermal and volumetric properties of waterlike molecules. A molecule is presented as a soft sphere with four directions in which hydrogen bonds can be formed. Two neighboring waters can interact through a van der Waals interaction or an orientation-dependent hydrogen-bonding interaction. For pure water, we explored properties such as molar volume, density, heat capacity, thermal expansion coefficient, and isothermal compressibility and found that the volumetric and thermal properties follow the same trends with temperature as in real water and are in good general agreement with Monte Carlo simulations. The model exhibits also two critical points for liquid-gas transition and transition between low-density and high-density fluid. Coexistence curves and a Widom line for the maximum and minimum in thermal expansion coefficient divides the phase space of the model into three parts: in one part we have gas region, in the second a high-density liquid, and the third region contains low-density liquid.

  1. Dispersive liquid-liquid microextraction of silver nanoparticles in water using ionic liquid 1-octyl-3-methylimidazolium hexafluorophosphate.

    Science.gov (United States)

    Chen, Sha; Sun, Yuanjing; Chao, Jingbo; Cheng, Liping; Chen, Yun; Liu, Jingfu

    2016-03-01

    Using the ionic liquid (IL) 1-octyl-3-methylimidazolium hexafluorophosphate as the extractant and methanol as the dispersion solvent, a dispersive liquid-liquid microextraction method was developed to extract silver nanoparticles (AgNPs) from environmental water samples. Parameters that influenced the extraction efficiency such as IL concentration, pH and extraction time were optimized. Under the optimized conditions, the highest extraction efficiency for AgNPs was above 90% with an enrichment factor of >90. The extracted AgNPs in the IL phase were identified by transmission electron microscopy and ultraviolet-visible spectroscopy, and quantified by inductively coupled plasma mass spectrometry after microwave digestion, with a detection limit of 0.01μg/L. The spiked recovery of AgNPs was 84.4% with a relative standard deviation (RSD) of 3.8% (n=6) at a spiked level of 5μg/L, and 89.7% with a RSD of 2.2% (n=6) at a spiked level of 300μg/L, respectively. Commonly existed environmental ions had a very limited influence on the extraction efficiency. The developed method was successfully applied to the analysis of AgNPs in river water, lake water, and the influent and effluent of a wastewater treatment plant, with recoveries in the range of 71.0%-90.9% at spiking levels of 0.11-4.7μg/L. Copyright © 2015. Published by Elsevier B.V.

  2. Binary, ternary and quaternary liquid-liquid equilibria in 1-butanol, oleic acid, water and n-heptane mixtures

    NARCIS (Netherlands)

    Winkelman, J. G. M.; Kraai, G. N.; Heeres, H. J.

    2009-01-01

    This work reports on liquid-liquid equilibria in the system 1-butanol, oleic acid, water and n-heptane used for biphasic, lipase catalysed esterifications. The literature was studied on the mutual solubility in binary systems of water and each of the organic components. Experimental results were

  3. Optically Thin Liquid Water Clouds: Their Importance and Our Challenge

    Science.gov (United States)

    Turner, D. D.; Vogelmann, A. M.; Austin, R. T.; Barnard, J. C.; Cady-Pereira, K.; Chiu, J. C.; Clough, S. A.; Flynn, C.; Khaiyer, M. M.; Liljegren, J.; hide

    2006-01-01

    Many of the clouds important to the Earth's energy balance, from the tropics to the Arctic, are optically thin and contain liquid water. Longwave and shortwave radiative fluxes are very sensitive to small perturbations of the cloud liquid water path (LWP) when the liquid water path is small (i.e., importance of these thin clouds to the Earth's energy balance, and explain the difficulties in observing them. In particular, because these clouds are optically thin, potentially mixed-phase, and often (i.e., have large 3-D variability), it is challenging to retrieve their microphysical properties accurately. We describe a retrieval algorithm intercomparison that was conducted to evaluate the issues involved. The intercomparison included eighteen different algorithms to evaluate their retrieved LWP, optical depth, and effective radii. Surprisingly, evaluation of the simplest case, a single-layer overcast cloud, revealed that huge discrepancies exist among the various techniques, even among different algorithms that are in the same general classification. This suggests that, despite considerable advances that have occurred in the field, much more work must be done, and we discuss potential avenues for future work.

  4. Emergence of the Coherent Structure of Liquid Water

    Directory of Open Access Journals (Sweden)

    Ivan Bono

    2012-07-01

    Full Text Available We examine in some detail the interaction of water molecules with the radiative electromagnetic field and find the existence of phase transitions from the vapor phase to a condensed phase where all molecules oscillate in unison, in tune with a self-trapped electromagnetic field within extended mesoscopic space regions (Coherence Domains. The properties of such a condensed phase are examined and found to be compatible with the phenomenological properties of liquid water. In particular, the observed value of critical density is calculated with good accuracy.

  5. Crossover between tetrahedral and hexagonal structures in liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Chara, Osvaldo [Instituto de Fisica de Liquidos y Sistemas Biologicos (IFLYSIB), CONICET - Universidad Nacional de La Plata (Argentina); McCarthy, Andres N., E-mail: amccarthy@iflysib.unlp.edu.a [Instituto de Fisica de Liquidos y Sistemas Biologicos (IFLYSIB), CONICET - Universidad Nacional de La Plata (Argentina); Grigera, J. Raul [Instituto de Fisica de Liquidos y Sistemas Biologicos (IFLYSIB), CONICET - Universidad Nacional de La Plata (Argentina)

    2011-01-17

    It is widely accepted that liquid water structure is comprised of two closely interweaved components; i.e. tetrahedral (low density) and hexagonal (high density) structures. The relative amount of these components is temperature and pressure dependent. We propose an order parameter, based on the radial distribution function, that quantifies the relative structural composition at any defined temperature and pressure, thus establishing the crossover point in structural dominance. At 300 K this point lies close to 2 kbar, pressure at which water looses most of its 'anomalous' properties.

  6. Inferring Large-Scale Terrestrial Water Storage Through GRACE and GPS Data Fusion in Cloud Computing Environments

    Science.gov (United States)

    Rude, C. M.; Li, J. D.; Gowanlock, M.; Herring, T.; Pankratius, V.

    2016-12-01

    Surface subsidence due to depletion of groundwater can lead to permanent compaction of aquifers and damaged infrastructure. However, studies of such effects on a large scale are challenging and compute intensive because they involve fusing a variety of data sets beyond direct measurements from groundwater wells, such as gravity change measurements from the Gravity Recovery and Climate Experiment (GRACE) or surface displacements measured by GPS receivers. Our work therefore leverages Amazon cloud computing to enable these types of analyses spanning the entire continental US. Changes in groundwater storage are inferred from surface displacements measured by GPS receivers stationed throughout the country. Receivers located on bedrock are anti-correlated with changes in water levels from elastic deformation due to loading, while stations on aquifers correlate with groundwater changes due to poroelastic expansion and compaction. Correlating linearly detrended equivalent water thickness measurements from GRACE with linearly detrended and Kalman filtered vertical displacements of GPS stations located throughout the United States helps compensate for the spatial and temporal limitations of GRACE. Our results show that the majority of GPS stations are negatively correlated with GRACE in a statistically relevant way, as most GPS stations are located on bedrock in order to provide stable reference locations and measure geophysical processes such as tectonic deformations. Additionally, stations located on the Central Valley California aquifer show statistically significant positive correlations. Through the identification of positive and negative correlations, deformation phenomena can be classified as loading or poroelastic expansion due to changes in groundwater. This method facilitates further studies of terrestrial water storage on a global scale. This work is supported by NASA AIST-NNX15AG84G (PI: V. Pankratius) and Amazon.

  7. What Determines the Ice Polymorph in Clouds?

    Science.gov (United States)

    Hudait, Arpa; Molinero, Valeria

    2016-07-20

    vapor in the tropical tropopause layer, and in polar stratospheric and noctilucent clouds. Our findings support and explain the evolution of the morphology of ice crystals from hexagonal to trigonal symmetry with decreasing temperature, as reported by experiments and in situ measurements in clouds. We conclude that selective growth of the elusive cubic ice polymorph by manipulation of the interfacial properties can likely be achieved at the ice-liquid interface but not at the ice-vapor interface.

  8. Selective extraction of emerging contaminants from water samples by dispersive liquid-liquid microextraction using functionalized ionic liquids.

    Science.gov (United States)

    Yao, Cong; Li, Tianhao; Twu, Pamela; Pitner, William R; Anderson, Jared L

    2011-03-25

    Functionalized ionic liquids containing the tris(pentafluoroethyl)trifluorophosphate (FAP) anion were used as extraction solvents in dispersive liquid-liquid microextraction (DLLME) for the extraction of 14 emerging contaminants from water samples. The extraction efficiencies and selectivities were compared to those of an in situ IL DLLME method which uses an in situ metathesis reaction to exchange 1-butyl-3-methylimidazolium chloride (BMIM-Cl) to 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide (BMIM-NTf(2)). Compounds containing tertiary amine functionality were extracted with high selectivity and sensitivity by the 1-(6-amino-hexyl)-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate (HNH(2)MPL-FAP) IL compared to other FAP-based ILs and the BMIM-NTf(2) IL. On the other hand, polar or acidic compounds without amine groups exhibited higher enrichment factors using the BMIM-NTf(2) IL. The detection limits for the studied analytes varied from 0.1 to 55.1 μg/L using the traditional IL DLLME method with the HNH(2)MPL-FAP IL as extraction solvent, and from 0.1 to 55.8 μg/L using in situ IL DLLME method with BMIM-Cl+LiNTf(2) as extraction solvent. A 93-fold decrease in the detection limit of caffeine was observed when using the HNH(2)MPL-FAP IL compared to that obtained using in situ IL DLLME method. Real water samples including tap water and creek water were analyzed with both IL DLLME methods and yielded recoveries ranging from 91% to 110%. Copyright © 2011 Elsevier B.V. All rights reserved.

  9. Ionic liquid foam floatation coupled with ionic liquid dispersive liquid-liquid microextraction for the separation and determination of estrogens in water samples by high-performance liquid chromatography with fluorescence detection.

    Science.gov (United States)

    Zhang, Rui; Wang, Chuanliu; Yue, Qiaohong; Zhou, Tiecheng; Li, Na; Zhang, Hanqi; Hao, Xiaoke

    2014-11-01

    An ionic liquid foam floatation coupled with ionic liquid dispersive liquid-liquid microextraction method was proposed for the extraction and concentration of 17-α-estradiol, 17-β-estradiol-benzoate, and quinestrol in environmental water samples by high-performance liquid chromatography with fluorescence detection. 1-Hexyl-3-methylimidazolium tetrafluoroborate was applied as foaming agent in the foam flotation process and dispersive solvent in microextraction. The introduction of the ion-pairing and salting-out agent NH4 PF6 was beneficial to the improvement of recoveries for the hydrophobic ionic liquid phase and analytes. Parameters of the proposed method including concentration of 1-hexyl-3-methylimidazolium tetrafluoroborate, flow rate of carrier gas, floatation time, types and concentration of ionic liquids, salt concentration in samples, extraction time, and centrifugation time were evaluated. The recoveries were between 98 and 105% with relative standard deviations lower than 7% for lake water and well water samples. The isolation of the target compounds from the water was found to be efficient, and the enrichment factors ranged from 4445 to 4632. This developing method is free of volatile organic solvents compared with regular extraction. Based on the unique properties of ionic liquids, the application of foam floatation, and dispersive liquid-liquid microextraction was widened. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Transformation of acidic poorly water soluble drugs into ionic liquids.

    Science.gov (United States)

    Balk, Anja; Wiest, Johannes; Widmer, Toni; Galli, Bruno; Holzgrabe, Ulrike; Meinel, Lorenz

    2015-08-01

    Poor water solubility of active pharmaceutical ingredients (API) is a major challenge in drug development impairing bioavailability and therapeutic benefit. This study is addressing the possibility to tailor pharmaceutical and physical properties of APIs by transforming these into tetrabutylphosphonium (TBP) salts, including the generation of ionic liquids (IL). Therefore, poorly water soluble acidic APIs (Diclofenac, Ibuprofen, Ketoprofen, Naproxen, Sulfadiazine, Sulfamethoxazole, and Tolbutamide) were converted into TBP ILs or low melting salts and compared to the corresponding sodium salts. Free acids and TBP salts were characterized by NMR and IR spectroscopy, DSC and XRPD, DVS and dissolution rate measurements, release profiles, and saturation concentration measurements. TBP salts had lower melting points and glass transition temperatures and dissolution rates were improved up to a factor of 1000 as compared to the corresponding free acid. An increase in dissolution rates was at the expense of increased hygroscopicity. In conclusion, the creation of TBP ionic liquids or solid salts from APIs is a valuable concept addressing dissolution and solubility challenges of poorly water soluble acidic compounds. The data suggested that tailor-made counterions may substantially expand the formulation scientist's armamentarium to meet challenges of poorly water soluble drugs. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Performance of Water-Based Liquid Scintillator: An Independent Analysis

    Directory of Open Access Journals (Sweden)

    D. Beznosko

    2014-01-01

    Full Text Available The water-based liquid scintillator (WbLS is a new material currently under development. It is based on the idea of dissolving the organic scintillator in water using special surfactants. This material strives to achieve the novel detection techniques by combining the Cerenkov rings and scintillation light, as well as the total cost reduction compared to pure liquid scintillator (LS. The independent light yield measurement analysis for the light yield measurements using three different proton beam energies (210 MeV, 475 MeV, and 2000 MeV for water, two different WbLS formulations (0.4% and 0.99%, and pure LS conducted at Brookhaven National Laboratory, USA, is presented. The results show that a goal of ~100 optical photons/MeV, indicated by the simulation to be an optimal light yield for observing both the Cerenkov ring and the scintillation light from the proton decay in a large water detector, has been achieved.

  12. Spectrophotometric determination of mercury in water samples after preconcentration using dispersive liquid-liquid microextraction.

    Science.gov (United States)

    Lemos, Valfredo Azevedo; dos Santos, Liz Oliveira; Silva, Eldevan dos Santos; Vieira, Emanuel Vitor dos Santos

    2012-01-01

    A simple method for the determination of mercury in water samples after preconcentration using dispersive liquid-liquid microextraction is described. The procedure is based on the extraction of mercury in the form of a complex and its subsequent determination by spectrophotometry. The complex is formed between Hg(II) and 2-(2-benzothiazolylazo)-p-cresol. The detection at 650 nm is performed directly in the metal-rich phase, which is spread on a triacetylcellulose membrane. The method eliminates the need to use a cuvet or large quantities of samples and reagents. The parameters that influence the preconcentration were studied, and the analytical characteristics were determined. The enrichment factor and the consumptive index for this method were 64 and 0.16 mL, respectively. The LOD (3.3 microg/L) and LOQ (11.1 microg/L) were also determined. The accuracy of the method was tested by the determination of mercury in certified reference materials BCR 397 (Human Hair) and SRM 2781 (Domestic Sludge). The method was applied to the determination of mercury in samples of drinking water, sea water, and river water.

  13. (Liquid + liquid) equilibria of (water + butyric acid + dibasic esters) ternary systems

    International Nuclear Information System (INIS)

    Kirbaslar, S. Ismail; Sahin, Selin; Bilgin, Mehmet

    2007-01-01

    (Liquid + liquid) equilibrium (LLE) data of the solubility (binodal) curves and tie-line end compositions were examined for mixtures of {water (1) + butyric acid (2) + dimethyl succinate or dimethyl glutarate or dimethyl adipate (3)} at T = 298.15 K and p = (101.3 ± 0.7) kPa. The relative mutual solubility of the butyric acid is higher in the dibasic esters layers than in the aqueous layer. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The LLE data of the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region

  14. (Liquid + liquid) equilibria of the (water + acetic acid + dibasic esters mixture) system

    Energy Technology Data Exchange (ETDEWEB)

    Ince, Erol [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)]. E-mail: erolince@istanbul.edu.tr

    2006-12-15

    (Liquid + liquid) equilibrium (LLE) data for the {l_brace}water + acetic acid + dibasic esters mixture (dimethyl adipate + dimethyl glutarate + dimethyl succinate){r_brace} system have been determined experimentally at T = (298.2, 308.2, and 318.2) K. Complete phase diagrams were obtained by determining solubility curve and tie-line data. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The UNIFAC model was used to predict the phase equilibrium in the system using the interaction parameters determined from experimental data between CH{sub 2}, CH{sub 3}COO, CH{sub 3}, COOH, and H{sub 2}O functional groups. Distribution coefficients and separation factors were compared with previous studies.

  15. (Liquid + liquid) equilibria of (water + propionic acid + dibasic esters) ternary systems

    Energy Technology Data Exchange (ETDEWEB)

    Kirbaslar, S. Ismail [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey); Ince, Erol [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)], E-mail: erolince@istanbul.edu.tr; Sahin, Selin; Dramur, Umur [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)

    2007-11-15

    (Liquid + liquid) equilibrium (LLE) data for the solubility curves and tie-line compositions were examined for mixtures of {l_brace}water (1) + propionic acid (2) + dimethyl succinate or dimethyl glutarate or dimethyl adipate (3){r_brace} at T = 298.15 K and atmospheric pressure, (101.3 {+-} 0.7) kPa. The relative mutual solubility of the propionic acid is higher in the dibasic esters phases than in the aqueous phase. The reliability of the experimental tie-line data were confirmed by using the Othmer-Tobias correlation. The LLE data of the ternary systems were predicted by UNIFAC and modified UNIFAC methods. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  16. (Liquid + liquid) equilibria of (water + butyric acid + isoamyl alcohol) ternary system

    Energy Technology Data Exchange (ETDEWEB)

    Bilgin, Mehmet [Engineering Faculty, Chemical Engineering Department, Istanbul University, Avcilar-Campus, 34320 Istanbul (Turkey); Ismail Kirbaslar, S. [Engineering Faculty, Chemical Engineering Department, Istanbul University, Avcilar-Campus, 34320 Istanbul (Turkey)]. E-mail: krbaslar@istanbul.edu.tr; Oezcan, Oender [Mustafa Nevzat Ilac San. AS., 34530 Yenibosna, Istanbul (Turkey); Dramur, Umur [Engineering Faculty, Chemical Engineering Department, Istanbul University, Avcilar-Campus, 34320 Istanbul (Turkey)

    2005-04-15

    (Liquid + liquid) equilibrium (LLE) data for the ternary system (water + butyric acid + isoamyl alcohol) have been determined experimentally at T (298.15, 308.15 and 318.15) K. Complete phase diagrams were obtained by determining solubility and the tie-line data. Tie-line compositions were correlated by Othmer-Tobias method. The UNIFAC method was used to predict the phase equilibrium in the system using the interaction parameters determined from experimental data between groups CH{sub 3}, CH{sub 2}, CH, COOH, OH and H{sub 2}O. It is found that UNIFAC group interaction parameters used for LLE could not provide a good prediction. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  17. (Liquid + liquid) equilibria of (water + butyric acid + dibasic esters) ternary systems

    Energy Technology Data Exchange (ETDEWEB)

    Kirbaslar, S. Ismail [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)]. E-mail: krbaslar@istanbul.edu.tr; Sahin, Selin [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey); Bilgin, Mehmet [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)

    2007-02-15

    (Liquid + liquid) equilibrium (LLE) data of the solubility (binodal) curves and tie-line end compositions were examined for mixtures of {l_brace}water (1) + butyric acid (2) + dimethyl succinate or dimethyl glutarate or dimethyl adipate (3){r_brace} at T = 298.15 K and p = (101.3 {+-} 0.7) kPa. The relative mutual solubility of the butyric acid is higher in the dibasic esters layers than in the aqueous layer. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The LLE data of the ternary systems were predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  18. Gas hydrate inhibition by perturbation of liquid water structure.

    Science.gov (United States)

    Sa, Jeong-Hoon; Kwak, Gye-Hoon; Han, Kunwoo; Ahn, Docheon; Lee, Kun-Hong

    2015-06-17

    Natural gas hydrates are icy crystalline materials that contain hydrocarbons, which are the primary energy source for this civilization. The abundance of naturally occurring gas hydrates leads to a growing interest in exploitation. Despite their potential as energy resources and in industrial applications, there is insufficient understanding of hydrate kinetics, which hinders the utilization of these invaluable resources. Perturbation of liquid water structure by solutes has been proposed to be a key process in hydrate inhibition, but this hypothesis remains unproven. Here, we report the direct observation of the perturbation of the liquid water structure induced by amino acids using polarized Raman spectroscopy, and its influence on gas hydrate nucleation and growth kinetics. Amino acids with hydrophilic and/or electrically charged side chains disrupted the water structure and thus provided effective hydrate inhibition. The strong correlation between the extent of perturbation by amino acids and their inhibition performance constitutes convincing evidence for the perturbation inhibition mechanism. The present findings bring the practical applications of gas hydrates significantly closer, and provide a new perspective on the freezing and melting phenomena of naturally occurring gas hydrates.

  19. Interplay of the Glass Transition and the Liquid-Liquid Phase Transition in Water

    Science.gov (United States)

    Giovambattista, Nicolas; Loerting, Thomas; Lukanov, Boris R.; Starr, Francis W.

    2012-01-01

    Water has multiple glassy states, often called amorphous ices. Low-density (LDA) and high-density (HDA) amorphous ice are separated by a dramatic, first-order like phase transition. It has been argued that the LDA-HDA transformation connects to a first-order liquid-liquid phase transition (LLPT) above the glass transition temperature Tg. Direct experimental evidence of the LLPT is challenging to obtain, since the LLPT occurs at conditions where water rapidly crystallizes. In this work, we explore the implications of a LLPT on the pressure dependence of Tg(P) for LDA and HDA by performing computer simulations of two water models – one with a LLPT, and one without. In the absence of a LLPT, Tg(P) for all glasses nearly coincide. When there is a LLPT, different glasses exhibit dramatically different Tg(P) which are directly linked with the LLPT. Available experimental data for Tg(P) are only consistent with the scenario including a LLPT. PMID:22550566

  20. Water sorption in ionic liquids: kinetics, mechanisms and hydrophilicity.

    Science.gov (United States)

    Cao, Yuanyuan; Chen, Yu; Sun, Xiaofu; Zhang, Zhongmin; Mu, Tiancheng

    2012-09-21

    Most of the ionic liquids (ILs) are hygroscopic in air. The effects of structural factors of ILs (cation, anion, alkyl chain length at cation, and C2 methylation at cation) and external factors (temperature, relative humidity, and impurity) on the kinetics of water sorption by 18 ILs were investigated. A modified two-step sorption mechanism was proposed to correlate the water sorption data in the ILs. Three type of parameters (sorption capacity, sorption rate and degree of difficulty to reach sorption equilibrium) based on the modified two-step mechanism were derived to comprehensively characterize the water sorption processes. These parameters have similar tendencies, providing an efficient way to evaluate them by one parameter that can be easily obtained. The hydrophilicity of the ILs was classified to four levels (super-high, high, medium, low) according to the water sorption capacity. The results show that cation of the ILs also plays an important role in water sorption, and the impurities affect the water sorption enormously. Acetate and halogen-based ILs have the highest hydrophilicity when combined with the imidazolium or pyridinium cation.

  1. Interfacial thermodynamics of water and six other liquid solvents.

    Science.gov (United States)

    Pascal, Tod A; Goddard, William A

    2014-06-05

    We examine the thermodynamics of the liquid-vapor interface by direct calculation of the surface entropy, enthalpy, and free energy from extensive molecular dynamics simulations using the two-phase thermodynamics (2PT) method. Results for water, acetonitrile, cyclohexane, dimethyl sulfoxide, hexanol, N-methyl acetamide, and toluene are presented. We validate our approach by predicting the interfacial surface tensions (IFT--excess surface free energy per unit area) in excellent agreement with the mechanical calculations using Kirkwood-Buff theory. Additionally, we evaluate the temperature dependence of the IFT of water as described by the TIP4P/2005, SPC/Ew, TIP3P, and mW classical water models. We find that the TIP4P/2005 and SPC/Ew water models do a reasonable job of describing the interfacial thermodynamics; however, the TIP3P and mW are quite poor. We find that the underprediction of the experimental IFT at 298 K by these water models results from understructured surface molecules whose binding energies are too weak. Finally, we performed depth profiles of the interfacial thermodynamics which revealed long tails that extend far into what would be considered bulk from standard Gibbs theory. In fact, we find a nonmonotonic interfacial free energy profile for water, a unique feature that could have important consequences for the absorption of ions and other small molecules.

  2. Reaction of water vapor with a clean liquid uranium surface

    International Nuclear Information System (INIS)

    Siekhaus, W.

    1985-01-01

    To study the reaction of water vapor with uranium, we have exposed clean liquid uranium surfaces to H 2 O under UHV conditions. We have measured the surface concentration of oxygen as a function of exposure, and determined the maximum attainable surface oxygen concentration X 0 /sup s/ as a function of temperature. We have used these measurements to estimate, close to the melting point, the solubility of oxygen (X 0 /sup b/, -4 ) and its surface segregation coefficient β/sup s/(> 10 3 ). 8 refs., 5 figs., 1 tab

  3. The structural origin of anomalous properties of liquid water

    Science.gov (United States)

    Nilsson, Anders; Pettersson, Lars G. M.

    2015-12-01

    Water is unique in its number of unusual, often called anomalous, properties. When hot it is a normal simple liquid; however, close to ambient temperatures properties, such as the compressibility, begin to deviate and do so increasingly on further cooling. Clearly, these emerging properties are connected to its ability to form up to four well-defined hydrogen bonds allowing for different local structural arrangements. A wealth of new data from various experiments and simulations has recently become available. When taken together they point to a heterogeneous picture with fluctuations between two classes of local structural environments developing on temperature-dependent length scales.

  4. Gastric emptying of liquids in rats dehydrated by water deprivation

    Directory of Open Access Journals (Sweden)

    Baracat E.C.E.

    1997-01-01

    Full Text Available The gastric emptying of liquids was investigated in male Wistar rats (8 to 10 weeks old, 210-300 g dehydrated by water deprivation. In this model of dehydration, weight loss, hematocrit and plasma density were significantly higher in the dehydrated animals than in the control groups after 48 and 72 h of water deprivation (P<0.05. Three test meals (saline (N = 10, water (N = 10 and a WHO rehydrating solution containing in one liter 90 mEq sodium, 20 mEq potassium, 80 mEq chloride and 30 mEq citrate (N = 10 were used to study gastric emptying following water deprivation for 24, 48 and 72 h. After 72 h, gastric emptying of the water (39.4% retention and rehydrating solution (49.2% retention test meals was significantly retarded compared to the corresponding control groups (P<0.05, Mann-Whitney test. The 72-h period of deprivation was used to study the recovery from dehydration, and water was supplied for 60 or 120 min after 67 h of deprivation. Body weight loss, hematocrit and plasma density tended to return to normal when water was offered for 120 min. In the animals supplied with water for 60 min, there was a recovery in the gastric emptying of water while the gastric emptying of the rehydrating solution was still retarded (53.1% retention; P<0.02, Kruskal-Wallis test. In the group supplied with water for 120 min, the gastric emptying of the rehydrating (51.7% retention and gluco-saline (46.0% retention solutions tended to be retarded (P = 0.04, Kruskal-Wallis test. In this model of dehydration caused by water deprivation, with little alteration in the body electrolyte content, gastric emptying of the rehydrating solution was retarded after rehydration with water. We conclude that the mechanisms whereby receptors in the duodenal mucosa can modify gastric motility are altered during dehydration caused by water deprivation

  5. Innovative Strategy on Hydrogen Evolution Reaction Utilizing Activated Liquid Water

    Science.gov (United States)

    Hwang, Bing-Joe; Chen, Hsiao-Chien; Mai, Fu-Der; Tsai, Hui-Yen; Yang, Chih-Ping; Rick, John; Liu, Yu-Chuan

    2015-11-01

    Splitting water for hydrogen production using light, or electrical energy, is the most developed ‘green technique’. For increasing efficiency in hydrogen production, currently, the most exciting and thriving strategies are focused on efficient and inexpensive catalysts. Here, we report an innovative idea for efficient hydrogen evolution reaction (HER) utilizing plasmon-activated liquid water with reduced hydrogen-bonded structure by hot electron transfer. This strategy is effective for all HERs in acidic, basic and neutral systems, photocatalytic system with a g-C3N4 (graphite carbon nitride) electrode, as well as in an inert system with an ITO (indium tin oxide) electrode. Compared to deionized water, the efficiency of HER increases by 48% based on activated water ex situ on a Pt electrode. Increase in energy efficiency from activated water is 18% at a specific current yield of -20 mA in situ on a nanoscale-granulated Au electrode. Moreover, the onset potential of -0.023 V vs RHE was very close to the thermodynamic potential of the HER (0 V). The measured current density at the corresponding overpotential for HER in an acidic system was higher than any data previously reported in the literature. This approach establishes a new vista in clean green energy production.

  6. Ultrafast Librational Relaxation of H2O in Liquid Water

    DEFF Research Database (Denmark)

    Petersen, Jakob; Møller, Klaus Braagaard; Rey, Rossend

    2013-01-01

    water molecules. The variation of the energy flow characteristics with rotational axis, initial rotational energy excitation magnitude, method of excitation, and temperature is discussed. Finally, the relation of the nonequilibrium results to equilibrium time correlations is investigated.......The ultrafast librational (hindered rotational) relaxation of a rotationally excited H2O molecule in pure liquid water is investigated by means of classical nonequilibrium molecular dynamics simulations and a power and work analysis. This analysis allows the mechanism of the energy transfer from...... hydration shell, dominated by those partners’ rotational motion, in a fairly symmetric fashion over the hydration shell. The minority component of the energy transfer, to these neighboring waters’ translational motion, exhibits an asymmetry in energy reception between hydrogen-bond-donating and -accepting...

  7. Solute Isotope Fractionation by Diffusion in Liquid Water

    Science.gov (United States)

    Bourg, I. C.; Sposito, G.

    2009-12-01

    In natural systems where molecular diffusion plays an important role, isotope distributions can be highly sensitive to the mass dependence of solute diffusion coefficients (D) in liquid water. Isotope geochemistry studies routinely assume that this mass-dependence (heretofore essentially unknown) either is negligible (as predicted by hydrodynamic theories) or follows a kinetic-theory-like inverse square root relation. However, experiments and molecular dynamics (MD) simulations show that the mass-dependence of D is intermediate between these hydrodynamic and kinetic theory predictions for alkali metals, alkaline earth metals, halides, and noble gases (Richter et al., 2006; Bourg and Sposito, 2007, 2008; Bourg et al., 2009). In this talk, we present a general description of the influence of solute valence and radius on the mass-dependence of D for mono-atomic solutes in liquid water. We explain the molecular-scale origin of this mass-dependence and highlight its applications in geochemistry and groundwater hydrology. Bourg I.C., and Sposito G. (2007) Geochim. Cosmochim. Acta 71, 5583-5589. Bourg I.C., and Sposito G. (2008) Geochim. Cosmochim. Acta 72, 2237-2247. Bourg I.C., Richter F.M., et al. (2009) Geochim. Cosmochim. Acta, in preparation. Richter F.M., Mendybaev R.A., et al. (2006) Geochim. Cosmochim. Acta 70, 277-289.

  8. Stability of amorphous silica-alumina in hot liquid water.

    Science.gov (United States)

    Hahn, Maximilian W; Copeland, John R; van Pelt, Adam H; Sievers, Carsten

    2013-12-01

    Herein, the hydrothermal stability of amorphous silica-alumina (ASA) is investigated under conditions relevant for the catalytic conversion of biomass, namely in liquid water at 200 °C. The hydrothermal stability of ASA is much higher than that of pure silica or alumina. Interestingly, the synthetic procedure used plays a major role in its resultant stability: ASA prepared by cogelation (CG) lost its microporous structure, owing to hydrolysis of the siloxane bonds, but the resulting mesoporous material still had a considerable surface area. ASA prepared by deposition precipitation (DP) contained a silicon-rich core and an aluminum-rich shell. In hot liquid water, the latter structure was transformed into a layer of amorphous boehmite, which protected the particle from further hydrolysis. The surface area showed relatively minor changes during the transformation. Independent of the synthetic method used, the ASAs retained a considerable concentration of acid sites. The concentration of acid sites qualitatively followed the changes in surface area, but the changes were less pronounced. The performance of different ASAs for the hydrolysis of cellobiose into glucose is compared. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Thermodynamic mechanism of density anomaly of liquid water

    Directory of Open Access Journals (Sweden)

    Makoto eYasutomi

    2015-03-01

    Full Text Available Although density anomaly of liquid water has long been studied by many different authors up to now, it is not still cleared what thermodynamic mechanism induces the anomaly. The thermodynamic properties of substances are determined by interparticle interactions. We analyze what characteristics of pair potential cause the density anomaly on the basis of statistical mechanics and thermodynamics using a thermodynamically self-consistent Ornstein-Zernike approximation (SCOZA. We consider a fluid of spherical particles with a pair potential given by a hard-core repulsion plus a soft-repulsion and an attraction. We show that the density anomaly occurs when the value of the soft-repulsive potential at hard-core contact is in some proper range, and the range depends on the attraction. Further, we show that the behavior of the excess internal energy plays an essential role in the density anomaly and the behavior is mainly determined by the values of the soft-repulsive potential, especially near the hard core contact. Our results show that most of ideas put forward up to now are not the direct causes of the density anomaly of liquid water.

  10. Distribution of binding energies of a water molecule in the water liquid-vapor interface

    Energy Technology Data Exchange (ETDEWEB)

    Chempath, Shaji [Los Alamos National Laboratory; Pratt, Lawrence R [TULANE UNIV

    2008-01-01

    Distributions of binding energies of a water molecule in the water liquid-vapor interface are obtained on the basis of molecular simulation with the SPC/E model of water. These binding energies together with the observed interfacial density profile are used to test a minimally conditioned Gaussian quasi-chemical statistical thermodynamic theory. Binding energy distributions for water molecules in that interfacial region clearly exhibit a composite structure. A minimally conditioned Gaussian quasi-chemical model that is accurate for the free energy of bulk liquid water breaks down for water molecules in the liquid-vapor interfacial region. This breakdown is associated with the fact that this minimally conditioned Gaussian model would be inaccurate for the statistical thermodynamics of a dilute gas. Aggressive conditioning greatly improves the performance of that Gaussian quasi-chemical model. The analogy between the Gaussian quasi-chemical model and dielectric models of hydration free energies suggests that naive dielectric models without the conditioning features of quasi-chemical theory will be unreliable for these interfacial problems. Multi-Gaussian models that address the composite nature of the binding energy distributions observed in the interfacial region might provide a mechanism for correcting dielectric models for practical applications.

  11. Ion Transfer Voltammetry Associated with Two Polarizable Interfaces Within Water and Moderately Hydrophobic Ionic Liquid Systems

    DEFF Research Database (Denmark)

    Gan, Shiyu; Zhou, Min; Zhang, Jingdong

    2013-01-01

    An electrochemical system composed of two polarizable interfaces (the metallic electrode|water and water|ionic liquid interfaces), namely two‐polarized‐interface (TPI) technique, has been proposed to explore the ion transfer processes between water and moderately hydrophobic ionic liquids (W|mIL)...

  12. Stable water isotopologue ratios in fog and cloud droplets of liquid clouds are not size-dependent

    Science.gov (United States)

    Spiegel, J.K.; Aemisegger, F.; Scholl, M.; Wienhold, F.G.; Collett, J.L.; Lee, T.; van Pinxteren, D.; Mertes, S.; Tilgner, A.; Herrmann, H.; Werner, Roland A.; Buchmann, N.; Eugster, W.

    2012-01-01

    In this work, we present the first observations of stable water isotopologue ratios in cloud droplets of different sizes collected simultaneously. We address the question whether the isotope ratio of droplets in a liquid cloud varies as a function of droplet size. Samples were collected from a ground intercepted cloud (= fog) during the Hill Cap Cloud Thuringia 2010 campaign (HCCT-2010) using a three-stage Caltech Active Strand Cloud water Collector (CASCC). An instrument test revealed that no artificial isotopic fractionation occurs during sample collection with the CASCC. Furthermore, we could experimentally confirm the hypothesis that the δ values of cloud droplets of the relevant droplet sizes (μm-range) were not significantly different and thus can be assumed to be in isotopic equilibrium immediately with the surrounding water vapor. However, during the dissolution period of the cloud, when the supersaturation inside the cloud decreased and the cloud began to clear, differences in isotope ratios of the different droplet sizes tended to be larger. This is likely to result from the cloud's heterogeneity, implying that larger and smaller cloud droplets have been collected at different moments in time, delivering isotope ratios from different collection times.

  13. Stable water isotopologue ratios in fog and cloud droplets of liquid clouds are not size-dependent

    Directory of Open Access Journals (Sweden)

    J. K. Spiegel

    2012-10-01

    Full Text Available In this work, we present the first observations of stable water isotopologue ratios in cloud droplets of different sizes collected simultaneously. We address the question whether the isotope ratio of droplets in a liquid cloud varies as a function of droplet size. Samples were collected from a ground intercepted cloud (= fog during the Hill Cap Cloud Thuringia 2010 campaign (HCCT-2010 using a three-stage Caltech Active Strand Cloud water Collector (CASCC. An instrument test revealed that no artificial isotopic fractionation occurs during sample collection with the CASCC. Furthermore, we could experimentally confirm the hypothesis that the δ values of cloud droplets of the relevant droplet sizes (μm-range were not significantly different and thus can be assumed to be in isotopic equilibrium immediately with the surrounding water vapor. However, during the dissolution period of the cloud, when the supersaturation inside the cloud decreased and the cloud began to clear, differences in isotope ratios of the different droplet sizes tended to be larger. This is likely to result from the cloud's heterogeneity, implying that larger and smaller cloud droplets have been collected at different moments in time, delivering isotope ratios from different collection times.

  14. The Relationship Between Dynamics and Structure in the Far Infrared Absorption Spectrum of Liquid Water

    Energy Technology Data Exchange (ETDEWEB)

    Woods, K.

    2005-01-14

    Using an intense source of far-infrared radiation, the absorption spectrum of liquid water is measured at a temperature ranging from 269 to 323 K. In the infrared spectrum we observe modes that are related to the local structure of liquid water. Here we present a FIR measured spectrum that is sensitive to the low frequency (< 100cm{sup -1}) microscopic details that exist in liquid water.

  15. The modelled liquid water balance of the Greenland Ice Sheet

    Science.gov (United States)

    Steger, Christian R.; Reijmer, Carleen H.; van den Broeke, Michiel R.

    2017-11-01

    Recent studies indicate that the surface mass balance will dominate the Greenland Ice Sheet's (GrIS) contribution to 21st century sea level rise. Consequently, it is crucial to understand the liquid water balance (LWB) of the ice sheet and its response to increasing surface melt. We therefore analyse a firn simulation conducted with the SNOWPACK model for the GrIS and over the period 1960-2014 with a special focus on the LWB and refreezing. Evaluations of the simulated refreezing climate with GRACE and firn temperature observations indicate a good model-observation agreement. Results of the LWB analysis reveal a spatially uniform increase in surface melt (0.16 m w.e. a-1) during 1990-2014. As a response, refreezing and run-off also indicate positive changes during this period (0.05 and 0.11 m w.e. a-1, respectively), where refreezing increases at only half the rate of run-off, implying that the majority of the additional liquid input runs off the ice sheet. This pattern of refreeze and run-off is spatially variable. For instance, in the south-eastern part of the GrIS, most of the additional liquid input is buffered in the firn layer due to relatively high snowfall rates. Modelled increase in refreezing leads to a decrease in firn air content and to a substantial increase in near-surface firn temperature. On the western side of the ice sheet, modelled firn temperature increases are highest in the lower accumulation zone and are primarily caused by the exceptional melt season of 2012. On the eastern side, simulated firn temperature increases are more gradual and are associated with the migration of firn aquifers to higher elevations.

  16. The modelled liquid water balance of the Greenland Ice Sheet

    Directory of Open Access Journals (Sweden)

    C. R. Steger

    2017-11-01

    Full Text Available Recent studies indicate that the surface mass balance will dominate the Greenland Ice Sheet's (GrIS contribution to 21st century sea level rise. Consequently, it is crucial to understand the liquid water balance (LWB of the ice sheet and its response to increasing surface melt. We therefore analyse a firn simulation conducted with the SNOWPACK model for the GrIS and over the period 1960–2014 with a special focus on the LWB and refreezing. Evaluations of the simulated refreezing climate with GRACE and firn temperature observations indicate a good model–observation agreement. Results of the LWB analysis reveal a spatially uniform increase in surface melt (0.16 m w.e. a−1 during 1990–2014. As a response, refreezing and run-off also indicate positive changes during this period (0.05 and 0.11 m w.e. a−1, respectively, where refreezing increases at only half the rate of run-off, implying that the majority of the additional liquid input runs off the ice sheet. This pattern of refreeze and run-off is spatially variable. For instance, in the south-eastern part of the GrIS, most of the additional liquid input is buffered in the firn layer due to relatively high snowfall rates. Modelled increase in refreezing leads to a decrease in firn air content and to a substantial increase in near-surface firn temperature. On the western side of the ice sheet, modelled firn temperature increases are highest in the lower accumulation zone and are primarily caused by the exceptional melt season of 2012. On the eastern side, simulated firn temperature increases are more gradual and are associated with the migration of firn aquifers to higher elevations.

  17. Development of Predictive Techniques for Estimating Liquid Water-Hydrate Equilibrium of Water-Hydrocarbon System

    Directory of Open Access Journals (Sweden)

    Amir H. Mohammadi

    2009-01-01

    Full Text Available In this communication, we review recent studies by these authors for modeling the -H equilibrium. With the aim of estimating the solubility of pure hydrocarbon hydrate former in pure water in equilibrium with gas hydrates, a thermodynamic model is introduced based on equality of water fugacity in the liquid water and hydrate phases. The solid solution theory of Van der Waals-Platteeuw is employed for calculating the fugacity of water in the hydrate phase. The Henry's law approach and the activity coefficient method are used to calculate the fugacities of the hydrocarbon hydrate former and water in the liquid water phase, respectively. The results of this model are successfully compared with some selected experimental data from the literature. A mathematical model based on feed-forward artificial neural network algorithm is then introduced to estimate the solubility of pure hydrocarbon hydrate former in pure water being in equilibrium with gas hydrates. Independent experimental data (not employed in training and testing steps are used to examine the reliability of this algorithm successfully.

  18. Use of Spacecraft Data to Drive Regions on Mars where Liquid Water would be Stable

    Science.gov (United States)

    Lobitz, Brad; Wood, Byron L.; Averner, Maurice M.; McKay, Christopher P.; MacElroy, Robert D.

    2001-01-01

    Combining Viking pressure and temperature data with Mars Orbital Laser Altimeter (MOLA) topography data we have computed the fraction of the martian year during which pressure and temperature allow for liquid water to be stable on the martian surface. We find that liquid water would be stable within the Hellas and Argyre basin and over the northern lowlands equatorward of about 40 degrees. The location with the maximum period of stable conditions for liquid water is in the southeastern portion of Utopia Planitia where 34% of the year liquid water would be stable if it was present. Locations of stability appear to correlate with the distribution of valley networks.

  19. Influence of liquid water and water vapor on antimisting kerosene (AMK)

    Science.gov (United States)

    Yavrouian, A. H.; Sarolouki, M.; Sarohia, V.

    1983-01-01

    Experiments have been performed to evaluate the compatibility of liquid water and water vapor with antimisting kerosenes (AMK) containing polymer additive FM-9 developed by Imperial Chemical Industries. This effort consists of the determination of water solubility in AMK, influence of water on restoration (degradation) of AMK, and effect of water on standard AMK quality control methods. The principal conclusions of this investigation are: (1) the uptake of water in AMK critically depends upon the degree of agitation and can be as high as 1300 ppm at 20 C, (2) more than 250 to 300 ppm of water in AMK causes an insoluble second phase to form. The amount of this second phase depends on fuel temperature, agitation, degree of restoration (degradation) and the water content of the fuel, (3) laboratory scale experiments indicate precipitate formation when water vapor comes in contact with cold fuel surfaces at a much lower level of water (125 to 150 ppm), (4) precipitate formation is very pronounced in these experiments where humid air is percolated through a cold fuel (-20 C), (5) laboratory tests further indicate that water droplet settling time is markedly reduced in AMK as compared to jet A, (6) limited low temperature testing down to -30 C under laboratory conditions indicates the formation of stable, transparent gels.

  20. Cloud Liquid Water, Mean Droplet Radius and Number Density Measurements Using a Raman Lidar

    Science.gov (United States)

    Whiteman, David N.; Melfi, S. Harvey

    1999-01-01

    A new technique for measuring cloud liquid water, mean droplet radius and droplet number density is outlined. The technique is based on simultaneously measuring Raman and Mie scattering from cloud liquid droplets using a Raman lidar. Laboratory experiments on liquid micro-spheres have shown that the intensity of Raman scattering is proportional to the amount of liquid present in the spheres. This fact is used as a constraint on calculated Mie intensity assuming a gamma function particle size distribution. The resulting retrieval technique is shown to give stable solutions with no false minima. It is tested using Raman lidar data where the liquid water signal was seen as an enhancement to the water vapor signal. The general relationship of retrieved average radius and number density is consistent with traditional cloud physics models. Sensitivity to the assumed maximum cloud liquid water amount and the water vapor mixing ratio calibration are tested. Improvements to the technique are suggested.

  1. Supercooled and glassy water: Metastable liquid(s), amorphous solid(s), and a no-man's land

    Science.gov (United States)

    Handle, Philip H.; Loerting, Thomas; Sciortino, Francesco

    2017-12-01

    We review the recent research on supercooled and glassy water, focusing on the possible origins of its complex behavior. We stress the central role played by the strong directionality of the water-water interaction and by the competition between local energy, local entropy, and local density. In this context we discuss the phenomenon of polyamorphism (i.e., the existence of more than one disordered solid state), emphasizing both the role of the preparation protocols and the transformation between the different disordered ices. Finally, we present the ongoing debate on the possibility of linking polyamorphism with a liquid-liquid transition that could take place in the no-man's land, the temperature-pressure window in which homogeneous nucleation prevents the investigation of water in its metastable liquid form.

  2. In situ separation of root hydraulic redistribution of soil water from liquid and vapor transport

    Science.gov (United States)

    Jeffrey M. Warren; J. Renée Brooks; Maria I. Dragila; Frederick C. Meinzer

    2011-01-01

    Nocturnal increases in water potential and water content in the upper soil profile are often attributed to root water efflux, a process termed hydraulic redistribution (HR). However, unsaturated liquid or vapor flux of water between soil layers independent of roots also contributes to the daily recovery in water content, confounding efforts to determine the actual...

  3. Investigation of the Extinguishing Features for Liquid Fuels and Organic Flammable Liquids Atomized by a Water Flow

    Science.gov (United States)

    Voytkov, Ivan V.; Zabelin, Maksim V.; Vysokomornaya, Olga V.

    2016-02-01

    The processes of heat and mass transfer were investigated experimentally while moving and evaporating the atomized water flow in high-temperature combustion products of typical liquid fuels and organic flammable liquids: gasoline, kerosene, acetone, crude oil, industrial alcohol. We determined typical periods of liquid extinguishing by an atomized water flow of various dispersability. Data of the discharge of extinguishing medium corresponding to various parameters of atomization and duration of using the atomization devices was presented. It is shown that Um≈3.5 m/s is a minimal outflow velocity of droplets during moving while passing the distance of 1m in the high-temperature gas medium to stop the combustion of organic liquids.

  4. Investigation of the Extinguishing Features for Liquid Fuels and Organic Flammable Liquids Atomized by a Water Flow

    Directory of Open Access Journals (Sweden)

    Voytkov Ivan V.

    2016-01-01

    Full Text Available The processes of heat and mass transfer were investigated experimentally while moving and evaporating the atomized water flow in high-temperature combustion products of typical liquid fuels and organic flammable liquids: gasoline, kerosene, acetone, crude oil, industrial alcohol. We determined typical periods of liquid extinguishing by an atomized water flow of various dispersability. Data of the discharge of extinguishing medium corresponding to various parameters of atomization and duration of using the atomization devices was presented. It is shown that Um≈3.5 m/s is a minimal outflow velocity of droplets during moving while passing the distance of 1m in the high-temperature gas medium to stop the combustion of organic liquids.

  5. Ultrapreconcentration and determination of organophosphorus pesticides in water by solid-phase extraction combined with dispersive liquid-liquid microextraction and high-performance liquid chromatography.

    Science.gov (United States)

    Chen, Junhua; Zhou, Guangming; Deng, Yongli; Cheng, Hongmei; Shen, Jie; Gao, Yi; Peng, Guilong

    2016-01-01

    Solid-phase extraction coupled with dispersive liquid-liquid microextraction was developed as an ultra-preconcentration method for the determination of four organophosphorus pesticides (isocarbophos, parathion-methyl, triazophos and fenitrothion) in water samples. The analytes considered in this study were rapidly extracted and concentrated from large volumes of aqueous solutions (100 mL) by solid-phase extraction coupled with dispersive liquid-liquid microextraction and then analyzed using high performance liquid chromatography. Experimental variables including type and volume of elution solvent, volume and flow rate of sample solution, salt concentration, type and volume of extraction solvent and sample solution pH were investigated for the solid-phase extraction coupled with dispersive liquid-liquid microextraction with these analytes, and the best results were obtained using methanol as eluent and ethylene chloride as extraction solvent. Under the optimal conditions, an exhaustive extraction for four analytes (recoveries >86.9%) and high enrichment factors were attained. The limits of detection were between 0.021 and 0.15 μg/L. The relative standard deviations for 0.5 μg/L of the pesticides in water were in the range of 1.9-6.8% (n = 5). The proposed strategy offered the advantages of simple operation, high enrichment factor and sensitivity and was successfully applied to the determination of four organophosphorus pesticides in water samples. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Ionic Liquid Dispersive Liquid-Liquid Microextraction Method for the Determination of Irinotecan, an Anticancer Drug, in Water and Urine Samples Using UV-Vis Spectrophotometry.

    Science.gov (United States)

    Uysal, Deniz; Karadaş, Cennet; Kara, Derya

    2017-05-01

    A new, simple, efficient, and environmentally friendly ionic liquid dispersive liquid-liquid microextraction method was developed for the determination of irinotecan, an anticancer drug, in water and urine samples using UV-Vis spectrophotometry. The ionic liquid 1-hexyl-3-methylimidazolium hexafluorophosphate was used as the extraction solvent, and ethanol was used as the disperser solvent. The main parameters affecting the extraction efficiency, including sample pH, volume of the ionic liquid, choice of the dispersive solvent and its volume, concentration of NaCl, and extraction and centrifugation times, were investigated and optimized. The effect of interfering species on the recovery of irinotecan was also examined. Under optimal conditions, the LOD (3σ) was 48.7 μg/L without any preconcentration. Because the urine sample was diluted 10-fold, the LOD for urine would be 487 μg/L. However, this could be improved 16-fold if preconcentration using a 40 mL aliquot of the sample is used. The proposed method was successfully applied to the determination of irinotecan in tap water, river water, and urine samples spiked with 10.20 mg/L for the water samples and 8.32 mg/L for the urine sample. The average recovery values of irinotecan determined were 99.1% for tap water, 109.4% for river water, and 96.1% for urine.

  7. Self Assembly of Ionic Liquids at the Air/Water Interface

    Czech Academy of Sciences Publication Activity Database

    Minofar, Babak

    2015-01-01

    Roč. 3, aug (2015), s. 27-40 ISSN 2245-4551 Institutional support: RVO:67179843 Keywords : Ionic liquids * air/ water interface * self assembly * ion- water interaction * ion-ion interaction Subject RIV: CE - Biochemistry

  8. Effectiveness of Liquid-Liquid Extraction, Solid Phase Extraction, and Headspace Technique for Determination of Some Volatile Water-Soluble Compounds of Rose Aromatic Water.

    Science.gov (United States)

    Canbay, Hale Seçilmiş

    2017-01-01

    Steam distillation is used to isolate scent of rose flowers. Rose aromatic water is commonly used in European cuisine and aromatherapy besides its use in cosmetic industry for its lovely scent. In this study, three different sampling techniques, liquid-liquid extraction (LLE), headspace technique (HS), and solid phase extraction (SPE), were compared for the analysis of volatile water-soluble compounds in commercial rose aromatic water. Some volatile water-soluble compounds of rose aromatic water were also analyzed by gas chromatography mass spectrometry (GCMS). In any case, it was concluded that one of the solid phase extraction methods led to higher recoveries for 2-phenylethyl alcohol (PEA) in the rose aromatic water than the liquid-liquid extraction and headspace technique. Liquid-liquid extraction method provided higher recovery ratios for citronellol, nerol, and geraniol than others. Ideal linear correlation coefficient values were observed by GCMS for quantitative analysis of volatile compounds ( r 2 ≥ 0.999). Optimized methods showed acceptable repeatability (RSDs 95%). For compounds such as α -pinene, linalool, β -caryophyllene, α -humulene, methyl eugenol, and eugenol, the best recovery values were obtained with LLE and SPE.

  9. Effectiveness of Liquid-Liquid Extraction, Solid Phase Extraction, and Headspace Technique for Determination of Some Volatile Water-Soluble Compounds of Rose Aromatic Water

    Directory of Open Access Journals (Sweden)

    Hale Seçilmiş Canbay

    2017-01-01

    Full Text Available Steam distillation is used to isolate scent of rose flowers. Rose aromatic water is commonly used in European cuisine and aromatherapy besides its use in cosmetic industry for its lovely scent. In this study, three different sampling techniques, liquid-liquid extraction (LLE, headspace technique (HS, and solid phase extraction (SPE, were compared for the analysis of volatile water-soluble compounds in commercial rose aromatic water. Some volatile water-soluble compounds of rose aromatic water were also analyzed by gas chromatography mass spectrometry (GCMS. In any case, it was concluded that one of the solid phase extraction methods led to higher recoveries for 2-phenylethyl alcohol (PEA in the rose aromatic water than the liquid-liquid extraction and headspace technique. Liquid-liquid extraction method provided higher recovery ratios for citronellol, nerol, and geraniol than others. Ideal linear correlation coefficient values were observed by GCMS for quantitative analysis of volatile compounds (r2≥0.999. Optimized methods showed acceptable repeatability (RSDs 95%. For compounds such as α-pinene, linalool, β-caryophyllene, α-humulene, methyl eugenol, and eugenol, the best recovery values were obtained with LLE and SPE.

  10. LIQUID-LIQUID EQUILIBRIA OF THE ACETIC ACID-WATER-MIXED SOLVENT (CYCLOHEXYL ACETATE-CYCLOHEXANOL SYSTEM

    Directory of Open Access Journals (Sweden)

    S. Çehreli

    2002-03-01

    Full Text Available Mixtures of cyclohexyl acetate and cyclohexanol were used as a mixed solvent to study liquid-liquid equilibria (LLE of the acetic acid-water-cyclohexanol-cyclohexyl acetate quaternary system. The solubility diagram and tie-line data were determined at 298±0.20 K and atmospheric pressure, using various compositions of mixed solvent. Reliability of the data was ascertained by making Othmer-Tobias and Hand plots.

  11. LIQUID-LIQUID EQUILIBRIA OF THE ACETIC ACID-WATER-MIXED SOLVENT (CYCLOHEXYL ACETATE-CYCLOHEXANOL) SYSTEM

    OpenAIRE

    Çehreli S.

    2002-01-01

    Mixtures of cyclohexyl acetate and cyclohexanol were used as a mixed solvent to study liquid-liquid equilibria (LLE) of the acetic acid-water-cyclohexanol-cyclohexyl acetate quaternary system. The solubility diagram and tie-line data were determined at 298±0.20 K and atmospheric pressure, using various compositions of mixed solvent. Reliability of the data was ascertained by making Othmer-Tobias and Hand plots.

  12. EXAMINATION OF LIQUID-LIQUID EQUILIBRIA OF WATER + ACETIC ACID + CYCLOHEXANOL TERNARIES AT 298, 303 AND 316 K

    OpenAIRE

    Beşir TATLI; Ş. İsmail KIRBAŞLAR; Metin HASDEMİR; F. Teoman MERİÇLİ

    2000-01-01

    Experimental liquid-liquid equilibria of water + acetic acid + cyclohexanol system was investigated at 298.16 ± 0.2, 303.16 ± 0.2 and 313.16 ± 0.2 K. The reliability of experimental tie-line data were ascertained through an Othmer-Tobias plot. Distribution coefficient was evaluated over the immiscibility region. It is concluded that the high boiling solvent cyclohexanol is suitable separating agent for dilute aqueous acetic acid solutions.

  13. EXAMINATION OF LIQUID-LIQUID EQUILIBRIA OF WATER + ACETIC ACID + CYCLOHEXANOL TERNARIES AT 298, 303 AND 316 K

    Directory of Open Access Journals (Sweden)

    Beşir TATLI

    2000-01-01

    Full Text Available Experimental liquid-liquid equilibria of water + acetic acid + cyclohexanol system was investigated at 298.16 ± 0.2, 303.16 ± 0.2 and 313.16 ± 0.2 K. The reliability of experimental tie-line data were ascertained through an Othmer-Tobias plot. Distribution coefficient was evaluated over the immiscibility region. It is concluded that the high boiling solvent cyclohexanol is suitable separating agent for dilute aqueous acetic acid solutions.

  14. Vapor-Liquid Equilibria of Imidazolium Ionic Liquids with Cyano Containing Anions with Water and Ethanol.

    Science.gov (United States)

    Khan, Imran; Batista, Marta L S; Carvalho, Pedro J; Santos, Luís M N B F; Gomes, José R B; Coutinho, João A P

    2015-08-13

    Isobaric vapor-liquid equilibria of 1-butyl-3-methylimidazolium thiocyanate ([C4C1im][SCN]), 1-butyl-3-methylimidazolium dicyanamide ([C4C1im][N(CN)2]), 1-butyl-3-methylimidazolium tricyanomethanide ([C4C1im][C(CN)3]), and 1-ethyl-3-methylimidazolium tetracyanoborate ([C2C1im][B(CN)4]), with water and ethanol were measured over the whole concentration range at 0.1, 0.07, and 0.05 MPa. Activity coefficients were estimated from the boiling temperatures of the binary systems, and the data were used to evaluate the ability of COSMO-RS for describing these molecular systems. Aiming at further understanding the molecular interactions on these systems, molecular dynamics (MD) simulations were performed. On the basis of the interpretation of the radial and spatial distribution functions along with coordination numbers obtained through MD simulations, the effect of the increase of CN-groups in the IL anion in its capability to establish hydrogen bonds with water and ethanol was evaluated. The results obtained suggest that, for both water and ethanol systems, the anion [N(CN)2](-) presents the higher ability to establish favorable interactions due to its charge, and that the ability of the anions to interact with the solvent, decreases with further increasing of the number of cyano groups in the anion. The ordering of the partial charges in the nitrogen atoms from the CN-groups in the anions agrees with the ordering obtained for VLE and activity coefficient data.

  15. Connecting thermodynamic and dynamical anomalies of water-like liquid-liquid phase transition in the Fermi-Jagla model

    Science.gov (United States)

    Higuchi, Saki; Kato, Daiki; Awaji, Daisuke; Kim, Kang

    2018-03-01

    We present a study using molecular dynamics simulations based on the Fermi-Jagla potential model, which is the continuous version of the mono-atomic core-softened Jagla model [J. Y. Abraham, S. V. Buldyrev, and N. Giovambattista, J. Phys. Chem. B 115, 14229 (2011)]. This model shows the water-like liquid-liquid phase transition between high-density and low-density liquids at the liquid-liquid critical point. In particular, the slope of the coexistence line becomes weakly negative, which is expected to represent one of the anomalies of liquid polyamorphism. In this study, we examined the density, dynamic, and thermodynamic anomalies in the vicinity of the liquid-liquid critical point. The boundaries of density, self-diffusion, shear viscosity, and excess entropy anomalies were characterized. Furthermore, these anomalies are connected according to Rosenfeld's scaling relationship between the excess entropy and the transport coefficients such as diffusion and viscosity. The results demonstrate the hierarchical and nested structures regarding the thermodynamic and dynamic anomalies of the Fermi-Jagla model.

  16. Hydrophobic zeolites for biofuel upgrading reactions at the liquid-liquid interface in water/oil emulsions.

    Science.gov (United States)

    Zapata, Paula A; Faria, Jimmy; Ruiz, M Pilar; Jentoft, Rolf E; Resasco, Daniel E

    2012-05-23

    HY zeolites hydrophobized by functionalization with organosilanes are much more stable in hot liquid water than the corresponding untreated zeolites. Silylation of the zeolite increases hydrophobicity without significantly reducing the density of acid sites. This hydrophobization with organosilanes makes the zeolites able to stabilize water/oil emulsions and catalyze reactions of importance in biofuel upgrading, i.e., alcohol dehydration and alkylation of m-cresol and 2-propanol in the liquid phase, at high temperatures. While at 200 °C the crystalline structure of an untreated HY zeolite collapses in a few hours in contact with a liquid medium, the functionalized hydrophobic zeolites keep their structure practically unaltered. Detailed XRD, SEM, HRTEM, and BET analyses indicate that even after reaction under severe conditions, the hydrophobic zeolites retain their crystallinity, surface area, microporosity, and acid density. It is proposed that by preferentially anchoring hydrophobic functionalities on the external surface, the direct contact of bulk liquid water and the zeolite is hindered, thus preventing the collapse of the framework during the reaction in liquid hot water.

  17. Hydrogen isotope separation in hydrophobic catalysts between hydrogen and liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Ye, Linsen, E-mail: yls2005@mail.ustc.edu.cn [China Academy of Engineering Physics, Mianyang 621900 (China); Luo, Deli [Science and Technology on Surface Physics and Chemistry Laboratory, Jiangyou 621907 (China); Tang, Tao; Yang, Wan; Yang, Yong [China Academy of Engineering Physics, Mianyang 621900 (China)

    2015-11-15

    Hydrogen isotope catalytic exchange between hydrogen and liquid water is a very effective process for deuterium-depleted potable water production and heavy water detritiation. To improve the characteristics of hydrophobic catalysts for this type of reaction, foamed and cellular structures of hydrophobic carbon-supported platinum catalysts were successfully prepared. Separation of deuterium or tritium from liquid water was carried out by liquid-phase catalytic exchange. At a gas–liquid ratio of 1.53 and exchange temperature of 70 °C, the theoretical plate height of the hydrophobic catalyst (HETP = 34.2 cm) was slightly lower than previously reported values. Changing the concentration of the exchange column outlet water yielded nonlinear changes in the height of the packing layer. Configurations of deuterium-depleted potable water and detritiation of heavy water provide references for practical applications.

  18. Hydrogen isotope separation in hydrophobic catalysts between hydrogen and liquid water

    International Nuclear Information System (INIS)

    Ye, Linsen; Luo, Deli; Tang, Tao; Yang, Wan; Yang, Yong

    2015-01-01

    Hydrogen isotope catalytic exchange between hydrogen and liquid water is a very effective process for deuterium-depleted potable water production and heavy water detritiation. To improve the characteristics of hydrophobic catalysts for this type of reaction, foamed and cellular structures of hydrophobic carbon-supported platinum catalysts were successfully prepared. Separation of deuterium or tritium from liquid water was carried out by liquid-phase catalytic exchange. At a gas–liquid ratio of 1.53 and exchange temperature of 70 °C, the theoretical plate height of the hydrophobic catalyst (HETP = 34.2 cm) was slightly lower than previously reported values. Changing the concentration of the exchange column outlet water yielded nonlinear changes in the height of the packing layer. Configurations of deuterium-depleted potable water and detritiation of heavy water provide references for practical applications.

  19. Modeling the liquid-liquid equilibria of water plus fluorocarbons with the cubic-plus-association equation of state

    DEFF Research Database (Denmark)

    Oliveira, Mariana B.; Freire, Mara G.; Marrucho, Isabel M.

    2007-01-01

    -plus-association equation of state (CPA EoS) has been extended to binary mixtures of water with several linear, cyclic, aromatic, and substituted fluorocarbons. The CPA EoS was successfully used to model the liquid-liquid equilibria of aqueous mixtures that contain FCs, while also being able to describe the cross...... dioxide, making them interesting for several biomedical applications. In most of these applications, water or aqueous systems are present for which the knowledge of the mutual solubilities between the fluorocarbons and the aqueous phases is important. In this work, the application of the cubic...

  20. Microwave-assisted liquid-liquid microextraction based on solidification of ionic liquid for the determination of sulfonamides in environmental water samples.

    Science.gov (United States)

    Song, Ying; Wu, Lijie; Lu, Chunmei; Li, Na; Hu, Mingzhu; Wang, Ziming

    2014-12-01

    An easy, quick, and green method, microwave-assisted liquid-liquid microextraction based on solidification of ionic liquid, was first developed and applied to the extraction of sulfonamides in environmental water samples. 1-Ethy-3-methylimidazolium hexafluorophosphate, which is a solid-state ionic liquid at room temperature, was used as extraction solvent in the present method. After microwave irradiation for 90 s, the solid-state ionic liquid was melted into liquid phase and used to finish the extraction of the analytes. The ionic liquid and sample matrix can be separated by freezing and centrifuging. Several experimental parameters, including amount of extraction solvent, microwave power and irradiation time, pH of sample solution, and ionic strength, were investigated and optimized. Under the optimum experimental conditions, good linearity was observed in the range of 2.00-400.00 μg/L with the correlation coefficients ranging from 0.9995 to 0.9999. The limits of detection for sulfathiazole, sulfachlorpyridazine, sulfamethoxazole, and sulfaphenazole were 0.39, 0.33, 0.62, and 0.85 μg/L, respectively. When the present method was applied to the analysis of environmental water samples, the recoveries of the analytes ranged from 75.09 to 115.78% and relative standard deviations were lower than 11.89%. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Liquid Water from First Principles: Validation of Different Sampling Approaches

    Energy Technology Data Exchange (ETDEWEB)

    Mundy, C J; Kuo, W; Siepmann, J; McGrath, M J; Vondevondele, J; Sprik, M; Hutter, J; Parrinello, M; Mohamed, F; Krack, M; Chen, B; Klein, M

    2004-05-20

    A series of first principles molecular dynamics and Monte Carlo simulations were carried out for liquid water to assess the validity and reproducibility of different sampling approaches. These simulations include Car-Parrinello molecular dynamics simulations using the program CPMD with different values of the fictitious electron mass in the microcanonical and canonical ensembles, Born-Oppenheimer molecular dynamics using the programs CPMD and CP2K in the microcanonical ensemble, and Metropolis Monte Carlo using CP2K in the canonical ensemble. With the exception of one simulation for 128 water molecules, all other simulations were carried out for systems consisting of 64 molecules. It is found that the structural and thermodynamic properties of these simulations are in excellent agreement with each other as long as adiabatic sampling is maintained in the Car-Parrinello molecular dynamics simulations either by choosing a sufficiently small fictitious mass in the microcanonical ensemble or by Nos{acute e}-Hoover thermostats in the canonical ensemble. Using the Becke-Lee-Yang-Parr exchange and correlation energy functionals and norm-conserving Troullier-Martins or Goedecker-Teter-Hutter pseudopotentials, simulations at a fixed density of 1.0 g/cm{sup 3} and a temperature close to 315 K yield a height of the first peak in the oxygen-oxygen radial distribution function of about 3.0, a classical constant-volume heat capacity of about 70 J K{sup -1} mol{sup -1}, and a self-diffusion constant of about 0.1 Angstroms{sup 2}/ps.

  2. Dissociative ionization of liquid water induced by vibrational overtone excitation

    International Nuclear Information System (INIS)

    Natzle, W.C.

    1983-03-01

    Photochemistry of vibrationally activated ground electronic state liquid water to produce H + and OH - ions has been initiated by pulsed, single-photon excitation of overtone and combination transitions. Transient conductivity measurements were used to determine quantum yields as a function of photon energy, isotopic composition, and temperature. The equilibrium relaxation rate following perturbation by the vibrationally activated reaction was also measured as a function of temperature reaction and isotopic composition. In H 2 O, the quantum yield at 283 +- 1 K varies from 2 x 10 -9 to 4 x 10 -5 for wave numbers between 7605 and 18140 cm -1 . In D 2 O, the dependence of quantum yield on wavelength has the same qualitative shape as for H 2 O, but is shifted to lower quantum yields. The position of a minimum in the quantum yield versus hydrogen mole fraction curve is consistent with a lower quantum yield for excitation of HOD in D 2 O than for excitation of D 2 O. The ionic recombination distance of 5.8 +- 0.5 A is constant within experimental error with temperature in H 2 O and with isotopic composition at 25 +- 1 0 C

  3. How well do we know the structure of liquid water?

    International Nuclear Information System (INIS)

    Pusztai, L.

    1999-01-01

    Complete text of publication follows. There have been numerous indications that there may be some problems with the generally accepted set of partial pair correlation functions (pcf) [1]. The origin of these problems is strongly related to the fact that for deriving the three partial pcf's of liquid water with direct separation, one needs to use at least one total structure factor (sf) of a (at least partially) hydrogenated sample. As an attempt to clarify the situation, most of the available data have been modelled by the Reverse Monte Carlo (RMC) technique, using the new code for flexible molecules [2]. It was found that, not surprisingly, neutron diffraction measurements of D 2 O and X-ray diffraction measurements on H 2 O (or D 2 O) [3] are in general the most reliable ones. Existing measurements on pure H 2 O - as it could be expected - should not be considered quantitatively. It is concluded that many different sets of partial pcf's could be generated, all of which are in better agreement with the original measured data than the presently accepted set. (author)

  4. Influence of the temperature on the (liquid + liquid) phase equilibria of (water + 1-propanl + linalool or geraniol)

    International Nuclear Information System (INIS)

    Wan, Li; Li, Hengde; Huang, Cheng; Feng, Yuqing; Chu, Guoqiang; Zheng, Yuying; Tan, Wei; Qin, Yanlin; Sun, Dalei; Fang, Yanxiong

    2017-01-01

    Highlights: • Ternary LLEs containing linalool and geraniol are presented. • Distribution ratios of 1-propanol in the mixtures are examined. • Influence of the temperature on the LLE is studied. • The LLE data were correlated using the NRTL and UNIQUAC models. - Abstract: Linalool and geraniol are the primary components of rose oil, palmarosa oil, and citronella oil and many other essential oils, and two important compounds used in the flavour and fragrance, cosmetic or pharmaceutical industries. Phase equilibria (LLE, VLE, solubility, etc.) and related thermodynamic properties of a mixture are essential in the processes design and control of mass transfer process. In this work, experimental (liquid + liquid) equilibria data of the systems (water + 1-propanl + linalool) and (water + 1-propanl + geraniol) are presented. The (liquid + liquid) equilibria of both systems were determined with a tie-line method at T = (283.15, 298.15 and 313.15) K under atmospheric pressure. The well-known Hand, Bachman and Othmer–Tobias equations were used to test the reliability of the experimental values. The influence of the temperature on the (liquid + liquid) phase equilibria of the mixtures, the binodal curves and distribution ratios of 1-propanl are shown and discussed. Moreover, the NRTL and UNIQUAC models were applied to fit the data for both ternary systems. The interaction parameters obtained from both models successfully correlated the equilibrium compositions. Furthermore, the ternary systems could be represented using the binary parameters of the thermodynamic model with a function of temperature.

  5. Looking for the rainbow on exoplanets covered by liquid and icy water clouds

    NARCIS (Netherlands)

    Karalidi, T.; Stam, D.M.; Hovenier, J.W.

    2012-01-01

    Aims. Looking for the primary rainbow in starlight that is reflected by exoplanets appears to be a promising method to search for liquid water clouds in exoplanetary atmospheres. Ice water clouds, that consist of water crystals instead of water droplets, could potentially mask the rainbow feature in

  6. Use of Dispersive Liquid-Liquid Microextraction and UV-Vis Spectrophotometry for the Determination of Cadmium in Water Samples

    Directory of Open Access Journals (Sweden)

    J. Pérez-Outeiral

    2014-01-01

    Full Text Available A simple and inexpensive method for cadmium determination in water using dispersive liquid-liquid microextraction and ultraviolet-visible spectrophotometry was developed. In order to obtain the best experimental conditions, experimental design was applied. Calibration was made in the range of 10–100 μg/L, obtaining good linearity (R2 = 0.9947. The obtained limit of detection based on calibration curve was 8.5 μg/L. Intra- and interday repeatability were checked at two levels, obtaining relative standard deviation values from 9.0 to 13.3%. The enrichment factor had a value of 73. Metal interferences were also checked and tolerable limits were evaluated. Finally, the method was applied to cadmium determination in real spiked water samples. Therefore, the method showed potential applicability for cadmium determination in highly contaminated liquid samples.

  7. Thermodynamic modeling of ternary and quaternary (liquid + liquid) systems containing water, FeCl3, HCl and diisopropyl ether

    NARCIS (Netherlands)

    Milosevic, M.; Hendriks, I.; Smits, R.E.R.; Schuur, Boelo; de Haan, A.B.

    2013-01-01

    Liquid–liquid extraction using ethers as solvents is a potentially energy saving alternative for the concentration of aqueous ferric chloride solutions. Adequate thermodynamic models that describe the behavior of the resulting quaternary systems (FeCl3, ether, acid and water) are not available in

  8. Separation of rate processes for isotopic exchange between hydrogen and liquid water in packed columns 10

    International Nuclear Information System (INIS)

    Butler, J.P.; Hartog, J. den; Goodale, J.W.; Rolston, J.H.

    1977-01-01

    Wetproofed platinum catalysts in packed columns promote isotopic exchange between counter-current streams of hydrogen saturated with water vapour and liquid water. The net rate of deuterium transfer from isotopically enriched hydrogen has been measured and separated into two rate processes involving the transfer of deuterium from hydrogen to water vapour and from water vapour to liquid. These are compared with independent measurements of the two rate processes to test the two-step successive exchange model for trickle bed reactors. The separated transfer rates are independent of bed height and characterize the deuterium concentrations of each stream along the length of the bed. The dependences of the transfer rates upon hydrogen and liquid flow, hydrogen pressure, platinum loading and the effect of dilution of the hydrophobic catalyst with inert hydrophilic packing are reported. The results indicate a third process may be important in the transfer of deuterium between hydrogen and liquid water. (author)

  9. Atmospheric mass and the record of liquid water on Mars

    Science.gov (United States)

    Halevy, I.; Head, J. W., III

    2017-12-01

    Widespread evidence for the action of liquid water on early Mars is generally accepted to require the presence of atmospheric greenhouse agents other than CO2. Much of this activity clusters in the late Noachian and early Hesperian (3.9-3.6 Ga), and appears to coincide with a long maximum in extrusive and explosive volcanic activity. Among other suggestions, a role for S-bearing volcanic gases has been proposed, but these and any other non-CO2 greenhouse gases or atmospheric components require a background CO2 atmosphere of several hundred mbar. Global climate models suggest that even if the surface reservoir of CO2 were much larger than today, this reservoir would be mostly trapped as CO2 ice, and only a few to tens of mbar would be in the atmosphere. Thus, at the long-term steady state, sustained warmth is difficult to achieve in the face of a fainter Sun. We suggest that episodic volcanism released the CO2 trapped as ice at the planet's surface in two ways. First, the emission of S-bearing greenhouse gases (mostly SO2) would lead to warming of a few Kelvins. Second, the deposition of volcanic ash on water and CO2 ice surfaces would push the local energy budget to favor sublimation, and would also decrease the planetary albedo and lead to additional warming. Inflation of the CO2 atmosphere has been shown in global climate models to shift the distribution of snowfall to high elevations, as opposed to a latitude-dependent distribution at low atmospheric pressure. We suggest that seasonal melting of this snow carved the valley networks and filled basin lakes. The duration of warm periods was limited by the timescale for atmospheric collapse by condensation, which is 102-103 years. Repeated inflation episodes over the duration of active volcanism led to an integrated duration of aqueous activity of 106-107 years, enough to carve the valley networks. The S-bearing gases emitted by eruptions formed sulfate minerals, initially uniformly dispersed, then remobilized and

  10. Homogeneous liquid-liquid extraction of metal ions with non-fluorinated bis(2-ethylhexyl)phosphate ionic liquids having a lower critical solution temperature in combination with water.

    Science.gov (United States)

    Depuydt, Daphne; Liu, Liwang; Glorieux, Christ; Dehaen, Wim; Binnemans, Koen

    2015-09-28

    Ionic liquids with an ether-functionalised cation and the bis(2-ethylhexyl)phosphate anion show thermomorphic behaviour in water, with a lower critical solution temperature. These ionic liquids are useful for homogeneous liquid-liquid extraction of first-row (3d) transition metals.

  11. Liquid-Liquid Equilibrium data for mono ethylene glycol extraction from water with the new ionic liquid tetraoctyl ammonium 2-methyl-1-naphtoate as solvent

    NARCIS (Netherlands)

    Garcia Chavez, L.Y.; Schuur, Boelo; de Haan, A.B.

    2012-01-01

    Thermal recovery of mono ethylene glycol (MEG) from aqueous streams is one of the most energy demanding operations in industry, because of the large amount of water that needs to be evaporated. The use of alternative technologies such as liquid–liquid extraction could save energy. A new tailor made

  12. Salt effect of KBr on the liquid-liquid equilibrium of the water/ethanol/1-pentanol system

    Directory of Open Access Journals (Sweden)

    Santos G.R.

    2000-01-01

    Full Text Available Liquid-liquid equilibrium data for the water/ethanol/1-pentanol/potassium bromide systems were experimentally determined at 25° C and 40ºC. The experimental data were correlated through the NRTL and UNIFAC-Dortmund models for the activity coefficient, with the estimation of new binary interaction parameters for both models, corresponding to the salt-solvent and solvent-solvent interactions for the NRTL model and the ion-ion and solvent-ion interactions for the UNIFAC-Dortmund model. The results obtained have shown that the NRTL model was more able to represent equilibrium data for the studied systems.

  13. Primitive Liquid Water of the Solar System in an Aqueous Altered Carbonaceous Chondrite

    Science.gov (United States)

    Tsuchiyama, A.; Miyake, A.; Kitayama, A.; Matsuno, J.; Takeuchi, A.; Uesugi, K.; Suzuki, Y.; Nakano, T.; Zolensky, M. E.

    2016-01-01

    Non-destructive 3D observations of the aqueous altered CM chondrite Sutter's Mill using scanning imaging x-ray microscopy (SIXM) showed that some of calcite and enstatite grains contain two-phase inclusion, which is most probably composed of liquid water and bubbles. This water should be primitive water responsible for aqueous alteration in an asteroid in the early solar system.

  14. Divergent trend in density versus viscosity of ionic liquid/water mixtures: a molecular view from guanidinium ionic liquids.

    Science.gov (United States)

    Singh, Akhil Pratap; Gardas, Ramesh L; Senapati, Sanjib

    2015-10-14

    Ionic liquids (ILs) have shown great potential in the dissolution and stability of biomolecules when a low-to-moderate quantity of water is added. Hence, determining the thermophysical properties and understanding these novel mixtures at the molecular level are of both fundamental and practical importance. In this context, here we report the synthesis of two nontoxic guanidinium cation based ILs, tetramethylguanidinium benzoate [TMG][BEN] and tetramethylguanidinium salicylate [TMG][SAL], and present a detailed comparison of their thermophysical properties in the presence of water. The results show that the [TMG][SAL]/water mixtures have higher density and higher apparent molar volume, but a lower viscosity and higher compressibility than the [TNG][BEN]/water mixtures. The measured viscosity and compressibility data are explained from ab initio quantum mechanical calculations and liquid-phase molecular dynamics simulations, where salicylate anions of denser [TMG][SAL]/water were found to exist as isolated ions due to intramolecular H-bonding. On the contrary, intermolecular H-bonding among the benzoate anions and their strong tendency to form an extended H-bonding network with water made [TMG][BEN]/water solutions more viscous and less compressible. This study shows the importance of probing these emerging solvents at the molecular-to-atomic level, which could be helpful in their optimal usage for task-specific applications.

  15. Thermal Conductivity of Liquid Water from Reverse Nonequilibrium Ab Initio Molecular Dynamics

    Science.gov (United States)

    Tsuchida, Eiji

    2018-02-01

    We report on a theoretical framework for calculating the thermal conductivity of liquid water from first principles with the aid of the linear scaling method. We also discuss the possibility of obtaining equilibrium properties from a nonequilibrium trajectory.

  16. On the implications of aerosol liquid water and phase separation for organic aerosol mass

    Data.gov (United States)

    U.S. Environmental Protection Agency — This dataset contains data presented in the figures of the paper "On the implications of aerosol liquid water and phase separation for organic aerosol mass"...

  17. Scanning Multichannel Microwave Radiometer (SMMR) Monthly Mean Atmospheric Liquid Water (ALW) By Prabhakara

    Data.gov (United States)

    National Aeronautics and Space Administration — SMMR_ALW_PRABHAKARA data are Special Multichannel Microwave Radiometer (SMMR) Monthly Mean Atmospheric Liquid Water (ALW) data by Prabhakara.The Prabhakara Scanning...

  18. Design of a process for supercritical water desalination with zero liquid discharge

    NARCIS (Netherlands)

    Odu, Samuel Obarinu; van der Ham, Aloysius G.J.; Metz, S.; Kersten, Sascha R.A.

    2015-01-01

    Conventional desalination methods have a major drawback; the production of a liquid waste stream which must be disposed. The treatment of this waste stream has always presented technical, economic, and environmental challenges. The supercritical water desalination (SCWD) process meets these

  19. Ab initio calculation of the electronic absorption spectrum of liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Martiniano, Hugo F. M. C.; Galamba, Nuno [Grupo de Física Matemática da Universidade de Lisboa, Av. Professor Gama Pinto 2, 1649-003 Lisboa (Portugal); Cabral, Benedito J. Costa, E-mail: ben@cii.fc.ul.pt [Grupo de Física Matemática da Universidade de Lisboa, Av. Professor Gama Pinto 2, 1649-003 Lisboa (Portugal); Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, 1749-016 Lisboa (Portugal); Instituto de Física da Universidade de São Paulo, CP 66318, 05314-970 São Paulo, SP (Brazil)

    2014-04-28

    The electronic absorption spectrum of liquid water was investigated by coupling a one-body energy decomposition scheme to configurations generated by classical and Born-Oppenheimer Molecular Dynamics (BOMD). A Frenkel exciton Hamiltonian formalism was adopted and the excitation energies in the liquid phase were calculated with the equation of motion coupled cluster with single and double excitations method. Molecular dynamics configurations were generated by different approaches. Classical MD were carried out with the TIP4P-Ew and AMOEBA force fields. The BLYP and BLYP-D3 exchange-correlation functionals were used in BOMD. Theoretical and experimental results for the electronic absorption spectrum of liquid water are in good agreement. Emphasis is placed on the relationship between the structure of liquid water predicted by the different models and the electronic absorption spectrum. The theoretical gas to liquid phase blue-shift of the peak positions of the electronic absorption spectrum is in good agreement with experiment. The overall shift is determined by a competition between the O–H stretching of the water monomer in liquid water that leads to a red-shift and polarization effects that induce a blue-shift. The results illustrate the importance of coupling many-body energy decomposition schemes to molecular dynamics configurations to carry out ab initio calculations of the electronic properties in liquid phase.

  20. Ab initio calculation of the electronic absorption spectrum of liquid water

    International Nuclear Information System (INIS)

    Martiniano, Hugo F. M. C.; Galamba, Nuno; Cabral, Benedito J. Costa

    2014-01-01

    The electronic absorption spectrum of liquid water was investigated by coupling a one-body energy decomposition scheme to configurations generated by classical and Born-Oppenheimer Molecular Dynamics (BOMD). A Frenkel exciton Hamiltonian formalism was adopted and the excitation energies in the liquid phase were calculated with the equation of motion coupled cluster with single and double excitations method. Molecular dynamics configurations were generated by different approaches. Classical MD were carried out with the TIP4P-Ew and AMOEBA force fields. The BLYP and BLYP-D3 exchange-correlation functionals were used in BOMD. Theoretical and experimental results for the electronic absorption spectrum of liquid water are in good agreement. Emphasis is placed on the relationship between the structure of liquid water predicted by the different models and the electronic absorption spectrum. The theoretical gas to liquid phase blue-shift of the peak positions of the electronic absorption spectrum is in good agreement with experiment. The overall shift is determined by a competition between the O–H stretching of the water monomer in liquid water that leads to a red-shift and polarization effects that induce a blue-shift. The results illustrate the importance of coupling many-body energy decomposition schemes to molecular dynamics configurations to carry out ab initio calculations of the electronic properties in liquid phase

  1. Magnetic retrieval of ionic liquids: fast dispersive liquid-liquid microextraction for the determination of benzoylurea insecticides in environmental water samples.

    Science.gov (United States)

    Zhang, Jiaheng; Li, Min; Yang, Miyi; Peng, Bing; Li, Yubo; Zhou, Wenfeng; Gao, Haixiang; Lu, Runhua

    2012-09-07

    A novel, rapid ionic liquid dispersive liquid-liquid microextraction (IL-DLLME) technique combined with magnetic retrieval (MR-IL-DLLME) has been developed and used to analyze five benzoylurea insecticides (BUs) in environmental water samples. This procedure was based on the magnetic retrieval of the ionic liquid using unmodified magnetic nanoparticles (MNPs). In this experiment, the fine ionic liquid droplets formed in aqueous samples functioned as an extractant for the extraction of BUs; after the extraction process was completed, Fe₃O₄ MNPs were added as a carrier to retrieve and separate the ionic liquid from the sample solution. After the supernatant was removed, the ionic liquid was desorbed using acetonitrile and subsequently injected directly into an HPLC system for analysis. The optimum experimental parameters are as follows: 20 mg of Fe₃O₄ (20 nm) as magnetic sorbents; 70 μL of [C₆MIM][PF₆] as the extraction solvent; 300 μL of acetonitrile as the disperser solvent; a vortex extraction time of 90 s with the vortex agitator set at 2800 rpm and no ionic strength. Under the optimized conditions, good linearity was obtained with correlation coefficients (r) greater than 0.9981. The repeatability and reproducibility of the proposed method were found to be good, and the limits of detection ranged from 0.05 μg L⁻¹ to 0.15 μg L⁻¹. The proposed method was then successfully used for the rapid determination of BUs in real water samples. The recoveries of five BUs at two spiked levels ranged from 79.8 to 91.7% with RSDs less than 6.0%. Copyright © 2012 Elsevier B.V. All rights reserved.

  2. Combustion characteristics of nanoaluminum, liquid water, and hydrogen peroxide mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Sabourin, J.L.; Yetter, R.A. [The Pennsylvania State University, Department of Mechanical and Nuclear Engineering, University Park, PA 16801 (United States); Risha, G.A. [The Pennsylvania State University, Division of Business and Engineering, Altoona, PA 16601 (United States); Son, S.F. [Purdue University, School of Mechanical Engineering, West Lafayette, IN 47907 (United States); Tappan, B.C. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)

    2008-08-15

    An experimental investigation of the combustion characteristics of nanoaluminum (nAl), liquid water (H{sub 2}O{sub (l)}), and hydrogen peroxide (H{sub 2}O{sub 2}) mixtures has been conducted. Linear and mass-burning rates as functions of pressure, equivalence ratio ({phi}), and concentration of H{sub 2}O{sub 2} in H{sub 2}O{sub (l)} oxidizing solution are reported. Steady-state burning rates were obtained at room temperature using a windowed pressure vessel over an initial pressure range of 0.24 to 12.4 MPa in argon, using average nAl particle diameters of 38 nm, {phi} from 0.5 to 1.3, and H{sub 2}O{sub 2} concentrations between 0 and 32% by mass. At a nominal pressure of 3.65 MPa, under stoichiometric conditions, mass-burning rates per unit area ranged between 6.93 g/cm{sup 2} s (0% H{sub 2}O{sub 2}) and 37.04 g/cm{sup 2} s (32% H{sub 2}O{sub 2}), which corresponded to linear burning rates of 9.58 and 58.2 cm/s, respectively. Burning rate pressure exponents of 0.44 and 0.38 were found for stoichiometric mixtures at room temperature containing 10 and 25% H{sub 2}O{sub 2}, respectively, up to 5 MPa. Burning rates are reduced above {proportional_to}5 MPa due to the pressurization of interstitial spaces of the packed reactant mixture with argon gas, diluting the fuel and oxidizer mixture. Mass burning rates were not measured above {proportional_to}32% H{sub 2}O{sub 2} due to an anomalous burning phenomena, which caused overpressurization within the quartz sample holder, leading to tube rupture. High-speed imaging displayed fingering or jetting ahead of the normal flame front. Localized pressure measurements were taken along the sample length, determining that the combustion process proceeded as a normal deflagration prior to tube rupture, without significant pressure buildup within the tube. In addition to burning rates, chemical efficiencies of the combustion reaction were determined to be within approximately 10% of the theoretical maximum under all conditions

  3. On the evaporation of superheated water drops formed by flashing of liquid jets

    International Nuclear Information System (INIS)

    Mutair, Sami; Ikegami, Yasuyuki

    2012-01-01

    The flash evaporation of superheated water in direct contact with its own vapor involves very high heat transfer rates and the existing solutions for the problems of heat diffusion in the superheated water drops underestimate the actual heat transfer rates, even when the gas-side heat transfer coefficient is assumed to be extremely high. This happens due to the poor thermal conductivity of the water which causes the heat transfer to be dominated by the heat flow within the liquid. Accommodation between the analytical results of the heat diffusion in superheated water and those obtained from the experimental measurements requires considering the effective thermal conductivity of the liquid owing to the violent nature of the flow, which is thought to be much larger than the mere molecular thermal conductivity. This paper presents initial attempts on modeling the liquid-side heat transfer process accompanying the surface evaporation of superheated water drops resulting from the flashing of superheated water jets. (authors)

  4. Compact Raman Lidar Measurement of Liquid and Vapor Phase Water Under the Influence of Ionizing Radiation

    Directory of Open Access Journals (Sweden)

    Shiina Tatsuo

    2016-01-01

    Full Text Available A compact Raman lidar has been developed for studying phase changes of water in the atmosphere under the influence of ionization radiation. The Raman lidar is operated at the wavelength of 349 nm and backscattered Raman signals of liquid and vapor phase water are detected at 396 and 400 nm, respectively. Alpha particles emitted from 241Am of 9 MBq ionize air molecules in a scattering chamber, and the resulting ions lead to the formation of liquid water droplets. From the analysis of Raman signal intensities, it has been found that the increase in the liquid water Raman channel is approximately 3 times as much as the decrease in the vapor phase water Raman channel, which is consistent with the theoretical prediction based on the Raman cross-sections. In addition, the radius of the water droplet is estimated to be 0.2 μm.

  5. Determination of trace amount of lead in industrial and municipal effluent water samples based on dispersive liquid-liquid extraction

    International Nuclear Information System (INIS)

    Shirkhanloo, H.; Sedighi, K.; Mousavi, H. Z.

    2014-01-01

    In this study, a simple, sensitive and accurate method was developed for the determination of lead ion by combining ionic liquid dispersive liquid-liquid extraction (Il-DLL E) with flame atomic absorption spectrometry. Tetraethyl thiuram disulfide (Tetd), acetone and 1-octyl-3m ethylimidazolium hexafluorophosphate [(C 8 MIM) (PF 6 )] were used as the chelating agent, dispersive and extraction solvent, respectively. Under the optimal conditions, the calibration graph was linear in the range of 5-190 μg L -1 of lead and the detection limit was 0.8 μg L -1 with a sample volume of 200 ml. The proposed method was validated by the analysis of one certified reference material and applied successfully to the determination of lead in real water samples. (Author)

  6. Determination of trace amount of lead in industrial and municipal effluent water samples based on dispersive liquid-liquid extraction

    Energy Technology Data Exchange (ETDEWEB)

    Shirkhanloo, H. [Iranian Petroleum Industry Health Research Institute, Occupational and Environmental Health Research Center, Tehran (Iran, Islamic Republic of); Sedighi, K.; Mousavi, H. Z., E-mail: hzmousavi@semnan.ac.ir [Semnan University, College of Science, Department of Chemistry, Semnan (Iran, Islamic Republic of)

    2014-10-01

    In this study, a simple, sensitive and accurate method was developed for the determination of lead ion by combining ionic liquid dispersive liquid-liquid extraction (Il-DLL E) with flame atomic absorption spectrometry. Tetraethyl thiuram disulfide (Tetd), acetone and 1-octyl-3m ethylimidazolium hexafluorophosphate [(C{sub 8}MIM) (PF{sub 6})] were used as the chelating agent, dispersive and extraction solvent, respectively. Under the optimal conditions, the calibration graph was linear in the range of 5-190 μg L{sup -1} of lead and the detection limit was 0.8 μg L{sup -1} with a sample volume of 200 ml. The proposed method was validated by the analysis of one certified reference material and applied successfully to the determination of lead in real water samples. (Author)

  7. Combination of solvent extractants for dispersive liquid-liquid microextraction of fungicides from water and fruit samples by liquid chromatography with tandem mass spectrometry.

    Science.gov (United States)

    Pastor-Belda, Marta; Garrido, Isabel; Campillo, Natalia; Viñas, Pilar; Hellín, Pilar; Flores, Pilar; Fenoll, José

    2017-10-15

    A multiresidue method was developed to determine twenty-five fungicides belonging to three different chemical families, oxazoles, strobilurins and triazoles, in water and fruit samples, using dispersive liquid-liquid microextraction (DLLME) and liquid chromatography/tandem mass spectrometry (LC-MS 2 ). Solid-liquid extraction with acetonitrile was used for the analysis in fruits, the extract being used as dispersant solvent in DLLME. Since some of the analytes showed high affinity for chloroform and the others were more efficiently extracted with undecanol, a mixture of both solvents was used as extractant in DLLME. After evaporation of CHCl 3 , the enriched phase was analyzed. Enrichment factors in the 23-119 and 12-60 ranges were obtained for waters and fruits, respectively. The approach was most sensitive for metominostrobin with limits of quantification of 1ngL -1 and 5ngkg -1 in waters and fruits, respectively, while a similar sensitivity was attained for tebuconazole in fruits. Recoveries of the fungicides varied between 86 and 116%. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. Levitation time measurement of water drops on the surface of liquid nitrogen

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Heetae; Lee, Younghee [Sungkyunkwan University, Suwon (Korea, Republic of); Cho, Hoonyoung [Dongguk University, Seoul (Korea, Republic of)

    2011-06-15

    The levitation of water drops on the surface of liquid nitrogen is studied. The water drop evaporates the liquid nitrogen, which makes a nitrogen vapor film between the water drop and the surface of the liquid nitrogen. The temperature of the drop falls from the initial temperature of the drop to the melting temperature and then eventually reaches the Leidenfrost temperature at which an ice sphere falls into the liquid nitrogen. The floating time of the water drop on the surface of liquid nitrogen corresponds to how long the temperature of the water drop takes to go from the initial temperature to the Leidenfrost temperature. We measured the floating time of the water drop on the surface of the liquid nitrogen as a function of the size of the drop and the initial temperature of the drop. The floating time increases linearly with increasing drop size and increases linearly with increasing initial temperature of drop, which can be explained reasonably well by assuming uniform cooling of the drop by heat conduction.

  9. Lost in Cloud

    Science.gov (United States)

    Maluf, David A.; Shetye, Sandeep D.; Chilukuri, Sri; Sturken, Ian

    2012-01-01

    Cloud computing can reduce cost significantly because businesses can share computing resources. In recent years Small and Medium Businesses (SMB) have used Cloud effectively for cost saving and for sharing IT expenses. With the success of SMBs, many perceive that the larger enterprises ought to move into Cloud environment as well. Government agency s stove-piped environments are being considered as candidates for potential use of Cloud either as an enterprise entity or pockets of small communities. Cloud Computing is the delivery of computing as a service rather than as a product, whereby shared resources, software, and information are provided to computers and other devices as a utility over a network. Underneath the offered services, there exists a modern infrastructure cost of which is often spread across its services or its investors. As NASA is considered as an Enterprise class organization, like other enterprises, a shift has been occurring in perceiving its IT services as candidates for Cloud services. This paper discusses market trends in cloud computing from an enterprise angle and then addresses the topic of Cloud Computing for NASA in two possible forms. First, in the form of a public Cloud to support it as an enterprise, as well as to share it with the commercial and public at large. Second, as a private Cloud wherein the infrastructure is operated solely for NASA, whether managed internally or by a third-party and hosted internally or externally. The paper addresses the strengths and weaknesses of both paradigms of public and private Clouds, in both internally and externally operated settings. The content of the paper is from a NASA perspective but is applicable to any large enterprise with thousands of employees and contractors.

  10. Glass transition of aqueous solutions involving annealing-induced ice recrystallization resolves liquid-liquid transition puzzle of water

    Science.gov (United States)

    Zhao, Li-Shan; Cao, Ze-Xian; Wang, Qiang

    2015-01-01

    Liquid-liquid transition of water is an important concept in condensed-matter physics. Recently, it was claimed to have been confirmed in aqueous solutions based on annealing-induced upshift of glass-liquid transition temperature, . Here we report a universal water-content, , dependence of for aqueous solutions. Solutions with vitrify/devitrify at a constant temperature, , referring to freeze-concentrated phase with left behind ice crystallization. Those solutions with totally vitrify at under conventional cooling/heating process though, of the samples annealed at temperatures   to effectively evoke ice recrystallization is stabilized at . Experiments on aqueous glycerol and 1,2,4-butanetriol solutions in literature were repeated, and the same samples subject to other annealing treatments equally reproduce the result. The upshift of by annealing is attributable to freeze-concentrated phase of solutions instead of ‘liquid II phase of water’. Our work also provides a reliable method to determine hydration formula and to scrutinize solute-solvent interaction in solution. PMID:26503911

  11. In Situ Characterization of Boehmite Particles in Water Using Liquid SEM.

    Science.gov (United States)

    Yao, Juan; Arey, Bruce W; Yang, Li; Zhang, Fei; Komorek, Rachel; Chun, Jaehun; Yu, Xiao-Ying

    2017-09-27

    In situ imaging and elemental analysis of boehmite (AlOOH) particles in water is realized using the System for Analysis at the Liquid Vacuum Interface (SALVI) and Scanning Electron Microscopy (SEM). This paper describes the method and key steps in integrating the vacuum compatible SAVLI to SEM and obtaining secondary electron (SE) images of particles in liquid in high vacuum. Energy dispersive x-ray spectroscopy (EDX) is used to obtain elemental analysis of particles in liquid and control samples including deionized (DI) water only and an empty channel as well. Synthesized boehmite (AlOOH) particles suspended in liquid are used as a model in the liquid SEM illustration. The results demonstrate that the particles can be imaged in the SE mode with good resolution (i.e., 400 nm). The AlOOH EDX spectrum shows significant signal from the aluminum (Al) when compared with the DI water and the empty channel control. In situ liquid SEM is a powerful technique to study particles in liquid with many exciting applications. This procedure aims to provide technical know-how in order to conduct liquid SEM imaging and EDX analysis using SALVI and to reduce potential pitfalls when using this approach.

  12. Calculation for liquid-liquid equilibria of quaternary alkane-ethyl acetate-methanol-water systems used in counter-current chromatography.

    Science.gov (United States)

    Chen, Jian; Zhao, Mengqiang; Yu, Yanmei; Li, Zongcheng

    2007-06-01

    The calculation of liquid-liquid equilibrium compositions of solvent systems is very important for the work on counter-current chromatography (CCC), especially the phase composition and volume ratio obtained from liquid-liquid equilibrium calculation. In this work, liquid-liquid equilibria of quaternary Arizona solvent systems, alkane-ethyl acetate-methanol-water, and related ternary systems are correlated and predicted using the non-random two-liquid model (NRTL). Hexane, heptane and isooctane are the used alkanes. The parameters in the model are regressed only with the special systems considered. Detailed comparison with experimental data shows that liquid-liquid equilibria of these systems can be predicted with greatly improved accuracy as compared to the group contribution method (UNIFAC).

  13. Selective extraction of copper, mercury, silver and palladium ionsfrom water using hydrophobic ionic liquids.

    Energy Technology Data Exchange (ETDEWEB)

    Papaiconomou, Nicolas; Lee, Jong-Min; Salminen, Justin; VonStosch, Moritz; Prausnitz, John M.

    2007-06-25

    Extraction of dilute metal ions from water was performed near room temperature with a variety of ionic liquids. Distribution coefficients are reported for fourteen metal ions extracted with ionic liquids containing cations 1-octyl-4-methylpyridinium [4MOPYR]{sup +}, 1-methyl-1-octylpyrrolidinium [MOPYRRO]{sup +} or 1-methyl-1-octylpiperidinium [MOPIP]{sup +}, and anions tetrafluoroborate [BF{sub 4}]{sup +}, trifluoromethyl sulfonate [TfO]{sup +} or nonafluorobutyl sulfonate [NfO]{sup +}. Ionic liquids containing octylpyridinium cations are very good for extracting mercury ions. However, other metal ions were not significantly extracted by any of these ionic liquids. Extractions were also performed with four new task-specific ionic liquids. Such liquids containing a disulfide functional group are efficient and selective for mercury and copper, whereas those containing a nitrile functional group are efficient and selective for silver and palladium.

  14. Granular flows at recurring slope lineae on Mars indicate a limited role for liquid water

    Science.gov (United States)

    Dundas, Colin M.; McEwen, Alfred S.; Chojnacki, Matthew; Milazzo, Moses P.; Byrne, Shane; McElwaine, Jim N.; Urso, Anna

    2017-12-01

    Recent liquid water flow on Mars has been proposed based on geomorphological features, such as gullies. Recurring slope lineae — seasonal flows that are darker than their surroundings — are candidate locations for seeping liquid water on Mars today, but their formation mechanism remains unclear. Topographical analysis shows that the terminal slopes of recurring slope lineae match the stopping angle for granular flows of cohesionless sand in active Martian aeolian dunes. In Eos Chasma, linea lengths vary widely and are longer where there are more extensive angle-of-repose slopes, inconsistent with models for water sources. These observations suggest that recurring slope lineae are granular flows. The preference for warm seasons and the detection of hydrated salts are consistent with some role for water in their initiation. However, liquid water volumes may be small or zero, alleviating planetary protection concerns about habitable environments.

  15. Process and apparatus for determining the proportion of water in a liquid containing petroleum

    International Nuclear Information System (INIS)

    Smith, H.D. Jr.; Arnold, D.M.

    1980-01-01

    This invention concerns nuclear techniques for determining the proportion or percentage of water contained in a petroleum stream and the salinity level of such water in oil refining and production operations. This technique consists in bombarding the liquid with fast neutrons from an appropriate source, these neutrons being slowed down to the point of becoming slow neutrons that can be captured by the substances present in the liquid thus giving rise to capture gamma rays. The energy spectrum of the gamma rays resulting from the capture of these slow or 'thermal' neutrons obtained in this manner, makes it possible to determine the presence of chlorine in the liquid and to measure its concentration so that if the degree of salinity of the liquid is known, the amount of salt water in it may be determined. Furthermore, the sulphur level can also be determined at the same time as the concentration of chlorine in certain conditions [fr

  16. Ionic liquid-based microwave-assisted dispersive liquid-liquid microextraction and derivatization of sulfonamides in river water, honey, milk, and animal plasma

    Energy Technology Data Exchange (ETDEWEB)

    Xu Xu; Su Rui; Zhao Xin; Liu Zhuang; Zhang Yupu; Li Dan; Li Xueyuan; Zhang Hanqi [College of Chemistry, Jilin University, Changchun 130012 (China); Wang Ziming, E-mail: analchem@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130012 (China)

    2011-11-30

    Graphical abstract: The extraction and derivatization efficiency of SAs is dependent on type and volume of extraction solvent, type and volume of disperser, microwave power and irradiation time, volume of derivatization reagent, pH of sample solution as well as ionic strength. Highlights: Black-Right-Pointing-Pointer A new, rapid and sensitive method for determining sulfonamides (SAs) was proposed. Black-Right-Pointing-Pointer Derivatization, extraction and preconcentration of SAs were performed in one step. Black-Right-Pointing-Pointer IL-based MADLLME and derivatization were first applied for the determination of SAs. Black-Right-Pointing-Pointer Trace SAs in river water, honey, milk, and pig plasma were determined. - Abstract: The ionic liquid-based microwave-assisted dispersive liquid-liquid microextraction (IL-based MADLLME) and derivatization was applied for the pretreatment of six sulfonamides (SAs) prior to the determination by high-performance liquid chromatography (HPLC). By adding methanol (disperser), fluorescamine solution (derivatization reagent) and ionic liquid (extraction solvent) into sample, extraction, derivatization, and preconcentration were continuously performed. Several experimental parameters, such as the type and volume of extraction solvent, the type and volume of disperser, amount of derivatization reagent, microwave power, microwave irradiation time, pH of sample solution, and ionic strength were investigated and optimized. When the microwave power was 240 W, the analytes could be derivatized and extracted simultaneously within 90 s. The proposed method was applied to the analysis of river water, honey, milk, and pig plasma samples, and the recoveries of analytes obtained were in the range of 95.0-110.8, 95.4-106.3, 95.0-108.3, and 95.7-107.7, respectively. The relative standard deviations varied between 1.5% and 7.3% (n = 5). The results showed that the proposed method was a rapid, convenient and feasible method for the determination

  17. Kapitza Resistance between Few-Layer Graphene and Water: Liquid Layering Effects

    DEFF Research Database (Denmark)

    Alexeev, Dmitry; Chen, Jie; Walther, Jens Honore

    2015-01-01

    difference in the phonon mean free path between the FLG and water. Remarkably, RK is strongly dependent on the layering of water adjacent to the FLG, exhibiting an inverse proportionality relationship to the peak density of the first water layer, which is consistent with better acoustic phonon matching...... between FLG and water. These findings suggest novel ways to engineer the thermal transport properties of solid−liquidinterfaces by controlling and regulating the liquid layering at the interface....

  18. Interfacial transport phenomena and stability in liquid-metal/water systems: scaling considerations

    International Nuclear Information System (INIS)

    Abdulla, S.; Liu, X.; Anderson, M.; Bonazza, R.; Corradini, M.; Cho, D.

    2001-01-01

    One concept being considered for steam generation in innovative nuclear reactor applications, involves water coming into direct contact with a circulating molten metal. The vigorous agitation of the two fluids, the direct liquid-liquid contact and the consequent large interfacial area give rise to very high heat transfer coefficients and rapid steam generation. For an optimum design of such direct contact heat exchange and vaporization systems, detailed knowledge is necessary of the various flow regimes, interfacial transport phenomena, heat transfer and operational stability. In this paper we describe current results from the first year of this research that studies the transport phenomena involved with the injection of water into molten metals (e.g., lead alloys). In particular, this work discusses scaling considerations related to direct contact heat exchange, our experimental plans for investigation and a test plan for the important experimental parameters; i.e., the water and liquid metal mass flow rates, the liquid metal pool temperature and the ambient pressure of the direct contact heat exchanger. Past experimental work and initial scaling results suggest that our experiments can directly represent the proper liquid metal pool temperature and the water subcooling. The experimental variation in water and liquid metal flow rates and system pressure (1-10 bar), although smaller than the current conceptual system designs, is sufficient to verify the expected scale effects to demonstrate the phenomena. (authors)

  19. Effect of water presence on choline chloride-2urea ionic liquid and coating platings from the hydrated ionic liquid

    Science.gov (United States)

    Du, Cuiling; Zhao, Binyuan; Chen, Xiao-Bo; Birbilis, Nick; Yang, Haiyan

    2016-07-01

    In the present study, hygroscopicity of the choline chloride-urea (ChCl-2Urea) ionic liquid (IL) was confirmed through Karl-Fisher titration examination, indicating that the water content in the hydrated ChCl-2Urea IL was exposure-time dependent and could be tailored by simple heating treatment. The impact of the absorbed water on the properties of ChCl-2Urea IL, including viscosity, electrical conductivity, electrochemical window and chemical structure was investigated. The results show that water was able to dramatically reduce the viscosity and improve the conductivity, however, a broad electrochemical window could be persisted when the water content was below ~6 wt.%. These characteristics were beneficial for producing dense and compact coatings. Nickel (Ni) coatings plating from hydrated ChCl-2Urea IL, which was selected as an example to show the effect of water on the electroplating, displayed that a compact and corrosion-resistant Ni coating was plated from ChCl-2Urea IL containing 6 wt.% water doped with 400 mg/L NA at a moderate temperature. As verified by FTIR analysis, the intrinsic reason could be ascribed that water was likely linked with urea through strong hydrogen bond so that the water decomposition was suppressed during plating. Present study may provide a reference to prepare some similar water-stable ILs for plating.

  20. Determination of bromoxynil and ioxynil in the presence of carbamates by supported liquid membrane-liquid chromatography in river waters

    Directory of Open Access Journals (Sweden)

    Titus Motswadi Maswabi

    2003-12-01

    Full Text Available Sample pre-treatment and enrichment using the supported liquid membrane (SLM technique for the determination of phenolic nitrile herbicides in presence of carbamates in river water samples was investigated. The uncharged herbicide molecules from the flowing aqueous solution diffuse through an immobilized water-immiscible organic solvent, supported by a porous polytetrafluoroethylene (PTFE membrane, and trapped in a stagnant acidic acceptor phase in an ionic form. Using n-undecane as a membrane solvent, the SLM extraction methodology was successfully used for the enrichment and separation of phenolic nitrile herbicides in environmental waters with extraction efficiencies of 60% or better. A RDS (% of 2.1 and 1.8 was obtained for the extraction of ioxynil and bromoxynil from river water, respectively.

  1. Are nanometric films of liquid undercooled interfacial water bio-relevant?

    Science.gov (United States)

    Möhlmann, Diedrich T F

    2009-06-01

    It is known that life processes below the melting point temperature can actively evolve and establish in micrometer-sized (and larger) veins and structures in ice and permafrost soil, filled with unfrozen water. Thermodynamic arguments and experimental results indicate the existence of much smaller nanometer sized thin films of undercooled liquid interfacial (ULI) water on surfaces of micrometer sized and larger mineral particles and microbes in icy environments far below the melting point temperature. This liquid interfacial water can be described in terms of a freezing point depression, which is due to the interfacial pressure of van der Waals forces. The physics behind the possibly also life supporting capability of nanometric films of undercooled liquid interfacial water, which also can "mantle" the surfaces of the much larger and micrometer-sized microbes, is discussed. As described, biological processes do not necessarily have to proceed in the "bulk" of the thin interfacial water, as in "vinical" water and in the micrometer sized veins e.g., but they can be supported or are even made possible already by covering thin mantles of liquid interfacial water. These can provide liquid water for metabolic processes and act as carrier for the necessary transport of nutrients and waste. ULI water supports two different and possibly biologically relevant transport processes: 2D molecular diffusion in the interfacial film, and flow-like due to regelation. ULI-water, which is "lost" by transport into microbes, e.g., will be refilled from the neighbouring ice. In this way, the nanometric liquid environment of microbes in ULI-water is comparable to that of microbes in bulk water. Another probably also biologically relevant property of ULI is, depending on the hydrophobic or hydrophilic character of the surfaces, that it is of lower density (LDL) or higher density (HDL) than bulk water. Furthermore, capillary effects and ions in ULI-water solutions can support, enhance, and

  2. Shallow transient liquid water environments on present-day mars, and their implications for life

    Science.gov (United States)

    Jones, Eriita G.

    2018-05-01

    The identification and characterisation of subsurface liquid water environments on Mars are of high scientific interest. Such environments have the potential to support microbial life, and, more broadly, to develop our understanding of the habitability of planets and moons beyond Earth. Given our current state of knowledge of life on Earth, three pre-requisites are necessary for an environment to be considered 'habitable' and therefore capable of supporting terrestrial-like life: energy, biogenic elements, and liquid water with a sufficiently high water activity. The surface of Mars today is predominately cold and dry, and any liquid water exposed to the atmosphere will vaporise or freeze on timescales of hours to days. These conditions have likely persisted for much of the last 10 million years, and perhaps longer. Despite this, briny liquid water flows (Recurrent Slope Linea) have been observed in a number of locations in the present-day. This review examines evidence from the Phoenix Lander (2008) and the Mars Science Laboratory (2012-current), to assess the occurrence of habitable conditions in the shallow Martian regolith. It will be argued that shallow, transient, liquid water brines are potentially habitable by microbial life, are likely a widespread occurrence on Mars, and that future exploration aimed at finding present-day habitable conditions and potential biology should 'follow the salt'.

  3. Ionic liquid based dispersive liquid-liquid microextraction coupled with micro-solid phase extraction of antidepressant drugs from environmental water samples.

    Science.gov (United States)

    Ge, Dandan; Lee, Hian Kee

    2013-11-22

    Ionic liquid-dispersive liquid-liquid microextraction combined with micro-solid phase extraction (IL-DLLME-μ-SPE), and high-performance liquid chromatography (HPLC) was developed for the determination of tricyclic antidepressants (TCAs) in water samples. Two hundred microliters of an organic solvent (as disperser solvent) and 20 μl of 1-hexyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate were injected into a 5.0 ml sample for sonication-assisted DLLME. After this, a μ-SPE device, containing a novel material zeolite imidazolate framework 4 (ZIF-4), was added into the sample solution and 1 min of vortex-assisted extraction was performed. After 5 min of sonication-assisted desorption, 10 μl of desorption solvent was injected into a HPLC system for analysis. A characteristic property of DLLME-VA-μ-SPE is that any organic solvent and solid sorbent immiscible with water can be used. Special apparatus, or conical-bottom test tubes, and tedious procedures conventionally associated with DLLME such as centrifugation, or refrigeration of solvent are not necessary in the present approach. A novel material, ZIF-4 was employed as μ-SPE sorbent. Under the optimized conditions, the calibration curves were linear in the range of 1-1000 μg/L. The relative standard deviations and the limits of detection were in the range of 1.5% and 7.8% and 0.3 and 1 μg/L, respectively. The relative recoveries of canal water samples, spiked with drugs, were in the range of 94.3% and 114.7%. The results showed that IL-DLLME-μ-SPE was suitable for the determination of TCAs in water samples. Copyright © 2013 Elsevier B.V. All rights reserved.

  4. Isobaric (vapour + liquid + liquid) equilibrium data for (di-n-propyl ether + n-propyl alcohol + water) and (diisopropyl ether + isopropyl alcohol + water) systems at 100 kPa

    Energy Technology Data Exchange (ETDEWEB)

    Lladosa, Estela [Departamento de Ingenieria Quimica, Escuela Tecnica Superior de Ingenieria, Universitat de Valencia, 46100 Burjassot, Valencia (Spain)], E-mail: estela.lladosa@uv.es; Monton, Juan B. [Departamento de Ingenieria Quimica, Escuela Tecnica Superior de Ingenieria, Universitat de Valencia, 46100 Burjassot, Valencia (Spain)], E-mail: juan.b.monton@uv.es; Burguet, MaCruz [Departamento de Ingenieria Quimica, Escuela Tecnica Superior de Ingenieria, Universitat de Valencia, 46100 Burjassot, Valencia (Spain)], E-mail: cruz.burguet@uv.es; Torre, Javier de la [Departamento de Ingenieria Quimica, Escuela Tecnica Superior de Ingenieria, Universitat de Valencia, 46100 Burjassot, Valencia (Spain)], E-mail: javier.torre@uv.es

    2008-05-15

    Isobaric (vapour + liquid + liquid) equilibria were measured for the (di-n-propyl ether + n-propyl alcohol + water) and (diisopropyl ether + isopropyl alcohol + water) system at 100 kPa. The apparatus used for the determination of (vapour + liquid + liquid) equilibrium data was an all-glass dynamic recirculating still with an ultrasonic homogenizer couple to the boiling flask. The experimental data demonstrated the existence of a heterogeneous ternary azeotrope for both ternary systems. The (vapour + liquid + liquid) equilibria data were found to be thermodynamically consistent for both systems. The experimental data were compared with the estimation using UNIQUAC and NRTL models and the prediction of UNIFAC model.

  5. Dynamics of nanoparticle self-assembly into superhydrophobic liquid marbles during water condensation.

    Science.gov (United States)

    Rykaczewski, Konrad; Chinn, Jeff; Walker, Marlon L; Scott, John Henry J; Chinn, Amy; Jones, Wanda

    2011-12-27

    Nanoparticles adsorbed onto the surface of a drop can fully encapsulate the liquid, creating a robust and durable soft solid with superhydrophobic characteristics referred to as a liquid marble. Artificially created liquid marbles have been studied for about a decade but are already utilized in some hair and skin care products and have numerous other potential applications. These soft solids are usually formed in small quantity by depositing and rolling a drop of liquid on a layer of hydrophobic particles but can also be made in larger quantities in an industrial mixer. In this work, we demonstrate that microscale liquid marbles can also form through self-assembly during water condensation on a superhydrophobic surface covered with a loose layer of hydrophobic nanoparticles. Using in situ environmental scanning electron microscopy and optical microscopy, we study the dynamics of liquid marble formation and evaporation as well as their interaction with condensing water droplets. We demonstrate that the self-assembly of nanoparticle films into three-dimensional liquid marbles is driven by multiple coalescence events between partially covered droplets and is aided by surface flows causing rapid nanoparticle film redistribution. We also show that droplet and liquid marble coalescence can occur due to liquid-to-liquid contact or squeezing of the two objects into each other as a result of compressive forces from surrounding droplets and marbles. Irrelevant of the mechanism, coalescence of marbles and drops can cause their rapid movement across and rolling off the edge of the surface. We also demonstrate that the liquid marbles randomly moving across the surface can be captured and immobilized by hydrophilic surface patterns.

  6. CALCULATED AND MEASURED VALUES OF LIQUID WATER CONTENT IN CLEAN AND POLLUTED ENVIRONMENTS

    Czech Academy of Sciences Publication Activity Database

    Fišák, Jaroslav; Řezáčová, Daniela; Mattanen, J.

    2006-01-01

    Roč. 50, č. 1 (2006), s. 121-130 ISSN 0039-3169 R&D Projects: GA AV ČR(CZ) IAA3042301 Institutional research plan: CEZ:AV0Z30420517 Keywords : liquid water content * visibility * air pollutant * fog /cloud water Subject RIV: DG - Athmosphere Sciences, Meteorology Impact factor: 0.603, year: 2006

  7. Calculation of Liquid Water-Hydrate-Methane Vapor Phase Equilibria from Molecular Simulations

    DEFF Research Database (Denmark)

    Jensen, Lars; Thomsen, Kaj; von Solms, Nicolas

    2010-01-01

    Monte Carlo simulation methods for determining fluid- and crystal-phase chemical potentials are used for the first time to calculate liquid water-methane hydrate-methane vapor phase equilibria from knowledge of atomistic interaction potentials alone. The water and methane molecules are modeled us...

  8. Efficiency and mechanism of demulsification of oil-in-water emulsions using ionic liquid

    NARCIS (Netherlands)

    Li, X.; Kersten, Sascha R.A.; Schuur, Boelo

    2016-01-01

    In this work, 13 ionic liquids (ILs), including 9 halogenide ILs and 4 non-halogenide ILs, were evaluated as demulsifiers for a model oil-in-water emulsion prepared with heptane and water, where sodium dodecylbenzenesulfonate (SDBS) was used as a surfactant. The separating efficiency (the fraction

  9. Automated dispersive liquid-liquid microextraction coupled to high performance liquid chromatography - cold vapour atomic fluorescence spectroscopy for the determination of mercury species in natural water samples.

    Science.gov (United States)

    Liu, Yao-Min; Zhang, Feng-Ping; Jiao, Bao-Yu; Rao, Jin-Yu; Leng, Geng

    2017-04-14

    An automated, home-constructed, and low cost dispersive liquid-liquid microextraction (DLLME) device that directly coupled to a high performance liquid chromatography (HPLC) - cold vapour atomic fluorescence spectroscopy (CVAFS) system was designed and developed for the determination of trace concentrations of methylmercury (MeHg + ), ethylmercury (EtHg + ) and inorganic mercury (Hg 2+ ) in natural waters. With a simple, miniaturized and efficient automated DLLME system, nanogram amounts of these mercury species were extracted from natural water samples and injected into a hyphenated HPLC-CVAFS for quantification. The complete analytical procedure, including chelation, extraction, phase separation, collection and injection of the extracts, as well as HPLC-CVAFS quantification, was automated. Key parameters, such as the type and volume of the chelation, extraction and dispersive solvent, aspiration speed, sample pH, salt effect and matrix effect, were thoroughly investigated. Under the optimum conditions, linear range was 10-1200ngL -1 for EtHg + and 5-450ngL -1 for MeHg + and Hg 2+ . Limits of detection were 3.0ngL -1 for EtHg + and 1.5ngL -1 for MeHg + and Hg 2+ . Reproducibility and recoveries were assessed by spiking three natural water samples with different Hg concentrations, giving recoveries from 88.4-96.1%, and relative standard deviations <5.1%. Copyright © 2017 Elsevier B.V. All rights reserved.

  10. Mixed reverse micelles facilitated downstream processing of lipase involving water-oil-water liquid emulsion membrane.

    Science.gov (United States)

    Bhowal, Saibal; Priyanka, B S; Rastogi, Navin K

    2014-01-01

    Our earlier work for the first time demonstrated that liquid emulsion membrane (LEM) containing reverse micelles could be successfully used for the downstream processing of lipase from Aspergillus niger. In the present work, we have attempted to increase the extraction and purification fold of lipase by using mixed reverse micelles (MRM) consisting of cationic and nonionic surfactants in LEM. It was basically prepared by addition of the internal aqueous phase solution to the organic phase followed by the redispersion of the emulsion in the feed phase containing enzyme, which resulted in globules of water-oil-water (WOW) emulsion for the extraction of lipase. The optimum conditions for maximum lipase recovery (100%) and purification fold (17.0-fold) were CTAB concentration 0.075 M, Tween 80 concentration 0.012 M, at stirring speed of 500 rpm, contact time 15 min, internal aqueous phase pH 7, feed pH 9, KCl concentration 1 M, NaCl concentration 0.1 M, and ratio of membrane emulsion to feed volume 1:1. Incorporation of the nonionic surfactant (e.g., Tween 80) resulted in remarkable improvement in the purification fold (3.1-17.0) of the lipase. LEM containing a mixture of nonionic and cationic surfactants can be successfully used for the enhancement in the activity recovery and purification fold during downstream processing of enzymes/proteins. © 2014 American Institute of Chemical Engineers.

  11. Study of Solid-Liquid Ratio of Fly Ash Geopolymer as Water Absorbent Material

    OpenAIRE

    Angga Prasetya Fandi; Candra Sukmana Ndaru; Anggarini Ufafa

    2017-01-01

    Geopolymer has been synthesized from fly ash to be applicated as water absorbent material. This research conducted to determine the ability of geopolymer to abrsop water by variation of solid – liquid ratio at optimum molarity of NaOH; 3 M. In this research, the synthesis of geopolymer was conducted at the variation of solid-liquid ratio; 60:40, 65:35, 70:30, and 75:25. Result of the treatment were characterized by XRD and SEM to compare the geopolymer structure. Water absorption capacity was...

  12. (Liquid + liquid) equilibria for the ternary (water + acetic acid + toluene) system at different temperatures: Experimental data and correlation

    International Nuclear Information System (INIS)

    Saien, Javad; Mozafarvandi, Maryam; Daliri, Shabnam; Norouzi, Mahdi

    2013-01-01

    Highlights: ► Solute distribution coefficient rises with temperature; however, mildly at low dosages. ► Solute extraction factor decreases with temperature, favoring extraction efficiency. ► A maximum separation is achieved at solute aqueous phase mass fraction of about 0.27. ► Both well known NRTL and UNIQUAC models predict the experimental data nicely. - Abstract: (Liquid + liquid) equilibrium (LLE) of the ternary (water + acetic acid + toluene) system was investigated at temperatures of (288.2, 298.2, and 313.2) K, under atmospheric pressure. This chemical system is frequently used in liquid–liquid extraction investigations. The results show that the distribution coefficient of acetic acid between organic and aqueous phases rises with increasing temperature, but the separation factor decreases within the temperature range covered. Meanwhile, a maximum extraction factor (about 100) was achieved for the solute aqueous phase mass fraction around 0.27 at T = 288.2 K. The tie line data for this system were sufficiently correlated by Othmer–Tobias and Hand equations. The experimental results were used to obtain binary interaction parameters as predicted by the non-random two liquid (NRTL) and universal quasi chemical (UNIQUAC) equation models using the Aspen Plus simulator. Root mean square deviation (RMSD) values as low as 0.0119 and 0.0139 were obtained for these models, respectively; indicating excellent correlation results for the provided experimental solubility data.

  13. Liquid-liquid equilibria for binary and ternary systems containing glycols, aromatic hydrocarbons, and water: Experimental measurements and modeling with the CPA EoS

    DEFF Research Database (Denmark)

    Folas, Georgios; Kontogeorgis, Georgios; Michelsen, Michael Locht

    2006-01-01

    Liquid-liquid equilibrium data of four binary glycol + aromatic hydrocarbon systems and three ternary systems containing water have been measured at atmospheric pressure. The measured systems are monoethylene glycol (MEG) + benzene or toluene, triethylene glycol (TEG) + benzene or toluene, MEG...... + water + benzene, MEG + water + toluene, and TEG + water + toluene. The binary systems are correlated with the Cubic-Plus-Association (CPA) equation of state while the ternary systems are predicted from interaction parameters obtained from the binary systems. Very satisfactory liquid-liquid equilibrium...... correlations are obtained for the binary systems using temperature-independent interaction parameters, while adequate predictions are achieved for multicomponent water + glycol + aromatic hydrocarbons systems when accounting for the solvation between the aromatic hydrocarbons and glycols or water....

  14. Mutual Solubilities of Ammonium-based Ionic Liquids with Water and with Water/Methanol Mixture

    Czech Academy of Sciences Publication Activity Database

    Machanová, Karolina; Jacquemin, J.; Wagner, Zdeněk; Bendová, Magdalena

    2012-01-01

    Roč. 42, SI (2012), s. 1229-1241 E-ISSN 1877-7058. [International Congress of Chemical and Process Engineering CHISA 2012 and 15th Conference PRES 2012 /20./. Prague, 25.08.2012-29.08.2012] Institutional support: RVO:67985858 Keywords : Ionic liquids * liquid-liquid equilibria * solubility Subject RIV: CF - Physical ; Theoretical Chemistry

  15. Molecular dynamics study of room temperature ionic liquids with water at mica surface

    Directory of Open Access Journals (Sweden)

    Huanhuan Zhang

    2018-04-01

    Full Text Available Water in room temperature ionic liquids (RTILs could impose significant effects on their interfacial properties at a charged surface. Although the interfaces between RTILs and mica surfaces exhibit rich microstructure, the influence of water content on such interfaces is little understood, in particular, considering the fact that RTILs are always associated with water due to their hygroscopicity. In this work, we studied how different types of RTILs and different amounts of water molecules affect the RTIL-mica interfaces, especially the water distribution at mica surfaces, using molecular dynamics (MD simulation. MD results showed that (1 there is more water and a thicker water layer adsorbed on the mica surface as the water content increases, and correspondingly the average location of K+ ions is farther from mica surface; (2 more water accumulated at the interface with the hydrophobic [Emim][TFSI] than in case of the hydrophilic [Emim][BF4] due to the respective RTIL hydrophobicity and ion size. A similar trend was also observed in the hydrogen bonds formed between water molecules. Moreover, the 2D number density map of adsorbed water revealed that the high-density areas of water seem to be related to K+ ions and silicon/aluminum atoms on mica surface. These results are of great importance to understand the effects of hydrophobicity/hydrophicility of RTIL and water on the interfacial microstructure at electrified surfaces. Keywords: Room temperature ionic liquids, Hydrophobicity/hydrophicility, Water content, Electrical double layer, Mica surface

  16. Beneficial effect of added water on sodium metal cycling in super concentrated ionic liquid sodium electrolytes

    Science.gov (United States)

    Basile, Andrew; Ferdousi, Shammi A.; Makhlooghiazad, Faezeh; Yunis, Ruhamah; Hilder, Matthias; Forsyth, Maria; Howlett, Patrick C.

    2018-03-01

    The plating and stripping performance of sodium metal in an ionic liquid electrolyte is improved when including water as an additive. Herein we report for the first time the trend of improved cycling behavior of Na0/+ in N-methyl-N-propylpyrrolidinium bis(fluorosulfonyl)imide with 500 ppm H2O. The addition of water to this ionic liquid electrolyte promotes the breakdown of the [FSI]- anion towards beneficial SEI formation. The benefits during plating and stripping of sodium is observed as lower total polarization during symmetrical cell cycling and decreased electrode/electrolyte interface impedance. Sodium metal surfaces after cycling with 500 ppm H2O are shown to be smooth in morphology in comparison to lower additive concentrations. The outcome of adventitious moisture benefiting Na0/+ cycling in an ionic liquid, contrary to conventional electrolytes, allows flexibility in ionic liquid electrolyte design to the benefit of battery manufacturers.

  17. (Liquid + liquid) equilibria of (water + propionic acid + diethyl succinate or diethyl glutarate or diethyl adipate) ternary systems

    Energy Technology Data Exchange (ETDEWEB)

    Kirbaslar, S. Ismail [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)], E-mail: krbaslar@istanbul.edu.tr; Sahin, Selin; Bilgin, Mehmet [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)

    2007-11-15

    (Liquid + liquid) equilibrium (LLE) data of the solubility (binodal) curves and tie-line end compositions were examined for {l_brace}water (1) + propionic acid (2) + diethyl succinate or diethyl glutarate or diethyl adipate (3){r_brace} at T = 298.15 K and 101.3 {+-} 0.7 kPa. The relative mutual solubility of the propionic acid is higher in the dibasic esters layers than in the aqueous layers. The reliability of the experimental tie-line data was confirmed by using the Othmer-Tobias correlation. The LLE data of the ternary systems was predicted by UNIFAC method. Distribution coefficients and separation factors were evaluated for the immiscibility region.

  18. Gas-liquid-liquid equilibria in mixtures of water, light gases, and hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Chao, K.C.

    1990-01-01

    Phase equilibrium in mixtures of water + light gases and water + heavy hydrocarbons has been investigated with the development of new local composition theory, new equations of state, and new experimental data. The preferential segregation and orientation of molecules due to different energies of molecular interaction has been simulated with square well molecules. Extensive simulation has been made for pure square well fluids and mixtures to find the local composition at wide ranges of states. A theory of local composition has been developed and an equation of state has been obtained for square well fluids. The new local composition theory has been embedded in several equations of state. The pressure of water is decoupled into a polar pressure and non-polar pressure according to the molecular model of water of Jorgensen et al. The polar pressure of water is combined with the BACK equation for the general description of polar fluids and their mixtures. Being derived from the steam table, the Augmented BACK equation is particularly suited for mixtures of water + non-polar substances such as the hydrocarbons. The hydrophobic character of the hydrocarbons had made their mixtures with water a special challenge. A new group contribution equation of state is developed to describe phase equilibrium and volumetric behavior of fluids while requiring only to know the molecular structure of the components. 15 refs., 1 fig.

  19. Disposal of liquid radioactive waste - discharge of radioactive waste waters from hospitals

    International Nuclear Information System (INIS)

    Ludwieg, F.

    1976-01-01

    A survey is given about legal prescriptions in the FRG concerning composition and amount of the liquid waste substances and waste water disposal by emitting into the sewerage, waste water decay systems and collecting and storage of patients excretions. The radiation exposure of the population due to drainage of radioactive waste water from hospitals lower by more than two orders than the mean exposure due to nuclear-medical use. (HP) [de

  20. Nanosecond Discharge in Bubbled Liquid n-Heptane: Effects of Gas Composition and Water Addition

    KAUST Repository

    Hamdan, Ahmad

    2016-08-30

    Recently, an aqueous discharge reactor was developed to facilitate reformation of liquid fuels by in-liquid plasma. To gain a microscopic understanding of the physical elements behind this aqueous reactor, we investigate nanosecond discharges in liquid n-heptane with single and double gaseous bubbles in the gap between electrodes. We introduce discharge probability (DP) to characterize the stochastic nature of the discharges, and we investigate the dependence of DP on the gap distance, applied voltage, gaseous bubble composition, and the water content in n-heptane/distilled-water emulsified mixtures. Propagation of a streamer through the bubbles indicates no discharges in the liquids. DP is controlled by the properties of the gaseous bubble rather than by the composition of the liquid mixture in the gap with a single bubble; meanwhile, DP is determined by the dielectric permittivity of the liquid mixture in the gap with double bubbles, results that are supported by static electric field simulations. We found that a physical mechanism of increasing DP is caused by an interaction between bubbles and an importance of the dielectric permittivity of a liquid mixture on the local enhancement of field intensity. We also discuss detailed physical characteristics, such as plasma lifetime and electron density within the discharge channel, by estimating from measured emissions with a gated-intensified charge-coupled device and by using spectroscopic images, respectively. © 1973-2012 IEEE.

  1. Stripping of acetone from water with microfabricated and membrane gas-liquid contactors.

    Science.gov (United States)

    Constantinou, Achilleas; Ghiotto, Francesco; Lam, Koon Fung; Gavriilidis, Asterios

    2014-01-07

    Stripping of acetone from water utilizing nitrogen as a sweeping gas in co-current flow was conducted in a microfabricated glass/silicon gas-liquid contactor. The chip consisted of a microchannel divided into a gas and a liquid chamber by 10 μm diameter micropillars located next to one of the channel walls. The channel length was 35 mm, the channel width was 220 μm and the microchannel depth 100 μm. The micropillars were wetted by the water/acetone solution and formed a 15 μm liquid film between them and the nearest channel wall, leaving a 195 μm gap for gas flow. In addition, acetone stripping was performed in a microchannel membrane contactor, utilizing a hydrophobic PTFE membrane placed between two microstructured acrylic plates. Microchannels for gas and liquid flows were machined in the plates and had a depth of 850 μm and 200 μm respectively. In both contactors the gas/liquid interface was stabilized: in the glass/silicon contactor by the hydrophilic micropillars, while in the PTFE/acrylic one by the hydrophobic membrane. For both contactors separation efficiency was found to increase by increasing the gas/liquid flow rate ratio, but was not affected when increasing the inlet acetone concentration. Separation was more efficient in the microfabricated contactor due to the very thin liquid layer employed.

  2. Substrate and surfactant effects on the glass-liquid transition of thin water films.

    Science.gov (United States)

    Souda, Ryutaro

    2006-09-07

    Temperature-programmed time-of-flight secondary ion mass spectrometry (TP-TOF-SIMS) and temperature-programmed desorption (TPD) have been used to perform a detailed investigation of the adsorption, desorption, and glass-liquid transition of water on the graphite and Ni(111) surfaces in the temperature range 13-200 K. Water wets the graphite surface at 100-120 K, and the hydrogen-bonded network is formed preferentially in the first monolayer to reduce the number of nonbonding hydrogens. The strongly chemisorbed water molecules at the Ni(111) surface do not form such a network and play a role in stabilizing the film morphology up to 160 K, where dewetting occurs abruptly irrespective of the film thickness. The surface structure of the water film formed on graphite is fluctuated considerably, resulting in deweting at 150-160 K depending on the film thickness. The dewetted patches of graphite are molecularly clean, whereas the chemisorbed water remains on the Ni(111) surface even after evaporation of the film. The abrupt drop in the desorption rate of water molecules at 160 K, which has been attributed to crystallization in the previous TPD studies, is found to disappear completely when a monolayer of methanol is present on the surface. This is because the morphology of supercooled liquid water is changed by the surface tension, and it is quenched by termination of the free OH groups on the surface. The surfactant methanol desorbs above 160 K since the hydrogen bonds of the water molecules are reconstructed. The drastic change in the properties of supercooled liquid water at 160 K should be ascribed to the liquid-liquid phase transition.

  3. Initiation of secondary ice production in clouds

    Science.gov (United States)

    Sullivan, Sylvia C.; Hoose, Corinna; Kiselev, Alexei; Leisner, Thomas; Nenes, Athanasios

    2018-02-01

    Disparities between the measured concentrations of ice-nucleating particles (INPs) and in-cloud ice crystal number concentrations (ICNCs) have led to the hypothesis that mechanisms other than primary nucleation form ice in the atmosphere. Here, we model three of these secondary production mechanisms - rime splintering, frozen droplet shattering, and ice-ice collisional breakup - with a six-hydrometeor-class parcel model. We perform three sets of simulations to understand temporal evolution of ice hydrometeor number (Nice), thermodynamic limitations, and the impact of parametric uncertainty when secondary production is active. Output is assessed in terms of the number of primarily nucleated ice crystals that must exist before secondary production initiates (NINP(lim)) as well as the ICNC enhancement from secondary production and the timing of a 100-fold enhancement. Nice evolution can be understood in terms of collision-based nonlinearity and the phasedness of the process, i.e., whether it involves ice hydrometeors, liquid ones, or both. Ice-ice collisional breakup is the only process for which a meaningful NINP(lim) exists (0.002 up to 0.15 L-1). For droplet shattering and rime splintering, a warm enough cloud base temperature and modest updraft are the more important criteria for initiation. The low values of NINP(lim) here suggest that, under appropriate thermodynamic conditions for secondary ice production, perturbations in cloud concentration nuclei concentrations are more influential in mixed-phase partitioning than those in INP concentrations.

  4. Simulation of Water Level Fluctuations in a Hydraulic System Using a Coupled Liquid-Gas Model

    Directory of Open Access Journals (Sweden)

    Chao Wang

    2015-08-01

    Full Text Available A model for simulating vertical water level fluctuations with coupled liquid and gas phases is presented. The Preissmann implicit scheme is used to linearize the governing equations for one-dimensional transient flow for both liquid and gas phases, and the linear system is solved using the chasing method. Some classical cases for single liquid and gas phase transients in pipelines and networks are studied to verify that the proposed methods are accurate and reliable. The implicit scheme is extended using a dynamic mesh to simulate the water level fluctuations in a U-tube and an open surge tank without consideration of the gas phase. Methods of coupling liquid and gas phases are presented and used for studying the transient process and interaction between the phases, for gas phase limited in a chamber and gas phase transported in a pipeline. In particular, two other simplified models, one neglecting the effect of the gas phase on the liquid phase and the other one coupling the liquid and gas phases asynchronously, are proposed. The numerical results indicate that the asynchronous model performs better, and are finally applied to a hydropower station with surge tanks and air shafts to simulate the water level fluctuations and air speed.

  5. Revisiting the total ion yield x-ray absorption spectra of liquid water microjets

    Energy Technology Data Exchange (ETDEWEB)

    Saykally, Richard J; Cappa, Chris D.; Smith, Jared D.; Wilson, Kevin R.; Saykally, Richard J.

    2008-02-16

    Measurements of the total ion yield (TIY) x-ray absorption spectrum (XAS) of liquid water by Wilson et al. (2002 J. Phys.: Condens. Matter 14 L221 and 2001 J. Phys. Chem. B 105 3346) have been revisited in light of new experimental and theoretical efforts by our group. Previously, the TIY spectrum was interpreted as a distinct measure of the electronic structure of the liquid water surface. However, our new results indicate that the previously obtained spectrum may have suffered from as yet unidentified experimental artifacts. Although computational results indicate that the liquid water surface should exhibit a TIY-XAS that is fundamentally distinguishable from the bulk liquid XAS, the new experimental results suggest that the observable TIY-XAS is actually nearly identical in appearance to the total electron yield (TEY-)XAS, which is a bulk probe. This surprising similarity between the observed TIY-XAS and TEY-XAS likely results from large contributions from x-ray induced electron stimulated desorption of ions, and does not necessarily indicate that the electronic structure of the bulk liquid and liquid surface are identical.

  6. Regional water implications of reducing oil imports with liquid transportation fuel alternatives in the United States.

    Science.gov (United States)

    Jordaan, Sarah M; Diaz Anadon, Laura; Mielke, Erik; Schrag, Daniel P

    2013-01-01

    The Renewable Fuel Standard (RFS) is among the cornerstone policies created to increase U.S. energy independence by using biofuels. Although greenhouse gas emissions have played a role in shaping the RFS, water implications are less understood. We demonstrate a spatial, life cycle approach to estimate water consumption of transportation fuel scenarios, including a comparison to current water withdrawals and drought incidence by state. The water consumption and land footprint of six scenarios are compared to the RFS, including shale oil, coal-to-liquids, shale gas-to-liquids, corn ethanol, and cellulosic ethanol from switchgrass. The corn scenario is the most water and land intense option and is weighted toward drought-prone states. Fossil options and cellulosic ethanol require significantly less water and are weighted toward less drought-prone states. Coal-to-liquids is an exception, where water consumption is partially weighted toward drought-prone states. Results suggest that there may be considerable water and land impacts associated with meeting energy security goals through using only biofuels. Ultimately, water and land requirements may constrain energy security goals without careful planning, indicating that there is a need to better balance trade-offs. Our approach provides policymakers with a method to integrate federal policies with regional planning over various temporal and spatial scales.

  7. Determination of estrogenic mycotoxins in environmental water samples by low-toxicity dispersive liquid-liquid microextraction and liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Emídio, Elissandro Soares; da Silva, Claudia Pereira; de Marchi, Mary Rosa Rodrigues

    2015-04-24

    A novel, simple, rapid and eco-friendly method based on dispersive liquid-liquid microextraction using a bromosolvent was developed to determine six estrogenic mycotoxins (zearalenone, zearalanone, α-zearalanol, β-zearalanol, α-zearalenol and β-zearalenol) in water samples by liquid chromatography-electrospray ionization tandem mass spectrometry in the negative mode (LC-ESI-MS/MS). The optimal conditions for this method include the use of 100 μL bromocyclohexane as an extraction solvent (using a non-dispersion solvent), 10 mL of aqueous sample (adjusted to pH 4), a vortex extraction time of 2 min, centrifugation for 10 min at 3500 rpm and no ionic strength adjustment. The calibration function was linear and was verified by applying the Mandel fitting test with a 95% confidence level. No matrix effect was observed. According to the relative standard deviations (RSDs), the precision was better than 13% for the repeatability and intermediate precision. The average recoveries of the spiked compounds ranged from 81 to 118%. The method limits of detection (LOD) and quantification (LOQ) considering a 125-fold pre-concentration step were 4-20 and 8-40 ng L(-1), respectively. Next, the method was applied to the analysis of the environmental aqueous samples, demonstrating the presence of β-zearalanol and zearalanone in the river water samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  8. Temperature-controlled liquid-liquid microextraction combined with high-performance liquid chromatography for the simultaneous determination of diazinon and fenitrothion in water and fruit juice samples.

    Science.gov (United States)

    Bazmandegan-Shamili, Alireza; Dadfarnia, Shayessteh; Shabani, Ali Mohammad Haji; Moghadam, Masoud Rohani; Saeidi, Mahboubeh

    2018-02-28

    A simple, environmentally benign, and rapid method based on temperature-controlled liquid-liquid microextraction using a deep eutectic solvent was developed for the simultaneous extraction/preconcentration of diazinon and fenitrothion. The method involved the addition of deep eutectic solvent to the aqueous sample followed by heating the mixture in a 75°C water bath until the solvent was completely dissolved in the aqueous phase. Then, the resultant solution was cooled in an ice bath and a cloudy solution was formed. Afterward, the mixture was centrifuged and the enriched deep eutectic solvent phase was analyzed by high-performance liquid chromatography with ultraviolet detection for quantification of the analytes. The factors affecting the extraction efficiency were optimized. Under the optimized extraction conditions, the limits of detection for diazinon and fenitrothion were 0.3 and 0.15 μg/L, respectively. The calibration curves for diazinon and fenitrothion exhibited linearity in the concentration range of 1-100 and 0.5-100 μg/L, respectively. The relative standard deviations for five replicate measurements at 10.0 μg/L level of analytes were less than 2.8 and 4.5% for intra- and interday assays, respectively. The developed method was successfully applied to the determination of diazinon and fenitrothion in water and fruit juice samples. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Simultaneous Design of Ionic Liquids and Azeotropic Separation for Systems Containing Water

    DEFF Research Database (Denmark)

    Roughton, Brock; Camarda, Kyle V.; Gani, Rafiqul

    , many separation tasks in the petrochemical and chemical industries involve separation of azeotropic mixtures. A common issue with the design and operation of these separation tasks is whether or not to use solvents? And, if solvents are to be used, what kind of solvent should be used and what would...... environmental impact would they cause? Ionic liquids show great promise for solvent-based separation, particularly for extractive distillation-based separations, due to their negligible vapor pressures and the fact that a wide range of solubilities and other properties can be obtained through structural changes....... Since a large number of azeotropes encountered include water as one of the compounds, the use of ionic liquids in solvent-based separation of water in azeotropic systems has been investigated. Along with the design of the ionic liquid being used to entrain water, the extractive distillation process has...

  10. The dielectric behaviour of snow: A study versus liquid water content

    Science.gov (United States)

    Ambach, W.; Denoth, A.

    1980-01-01

    Snow is treated as a heterogeneous dielectric material consisting of ice, air, and water. The greater difference in the high frequency relative permittivity of dry snow and water allows to determine the liquid water content by measurements of the relative permittivity of snow. A plate condenser with a volume of about 1000 cv cm was used to measure the average liquid water content in a snow volume. Calibration was carried out using a freezing calorimeter. In order to measure the liquid water content in thin snow layers, a comb-shaped condenser was developed, which is the two dimensional analogon of the plate condenser. With this moisture meter the liquid water content was measured in layers of a few millimeters in thickness, whereby the effective depth of measurement is given by the penetration depth of electric field lines which is controlled by the spacing of the strip lines. Results of field measurements with both moisture meters, the plate condenser and the comb-shaped condenser, are given.

  11. Freely accessible water does not decrease consumption of ethanol liquid diets.

    Science.gov (United States)

    de Fiebre, NancyEllen C; de Fiebre, Christopher M

    2003-02-01

    In experimental studies, liquid ethanol diets are usually given as the sole source of nutrition and fluid. Two series of experiments were conducted to examine the effect of freely accessible water on the consumption of ethanol liquid diets in male Long-Evans rats. The consumption of diets and subsequent learning ability of rats were first examined in animals given twice-daily saline injections. One group received diet with no access to water for 12 weeks and was subsequently given free access to water with diets for an additional 12 weeks. A second group was given diet and water ad libitum for 24 weeks. Control animals received an isocaloric sucrose-containing diet (with or without ad libitum access to water). Subsequently, rats were tested for active avoidance learning. In the first 12 weeks, animals with ad libitum access to water drank more diet than did water-restricted animals, and previously water-restricted animals increased their diet consumption when access to water was freely available. All water-restricted animals, in both ethanol- and sucrose-treated groups, showed deficits in active avoidance learning, whereas only ethanol-treated animals in groups with ad libitum access to water showed learning deficits. In the second series of experiments, the effect of saline injections on diet consumption, both in the presence and absence of water, was examined. Although saline injections were associated with decreased diet consumption, there was no effect of free access to water. No differences in blood ethanol concentration were seen among groups. Findings obtained from both series of studies demonstrate that consumption of a Sustacal-based liquid ethanol diet does not decrease if access to water is freely available.

  12. An attempt to monitor liquid water content in seasonal snow using capacitance probes

    Science.gov (United States)

    Avanzi, Francesco; Caruso, Marco; Jommi, Cristina; De Michele, Carlo; Ghezzi, Antonio

    2015-04-01

    Liquid water dynamics in snow are a key factor in wet snow avalanche triggering, in ruling snowmelt runoff timing and amounts, and in remote sensing interpretation. It follows that a continuous-time monitoring of this variable would be very desirable. Nevertheless, such an operation is nowadays hampered by the difficulty in obtaining direct, precise and continuous-time measurements of this quantity without perturbing the snowpack itself. As a result, only a few localized examples exist of continuous-time measurements of this variable. In this framework, we tried to get undisturbed measurements of liquid water content using capacitance probes. These instruments were originally designed to obtain liquid water content data in soils. After being installed on a support and driven in the snow, they include part of the medium under investigation in a LC circuit. The resonant frequency of the circuit depends on liquid water content, hence its measurement. To test these sensors, we designed two different field surveys (in April 2013 and April 2014) at a medium elevation site (around 1980 m a.s.l.). In both the cases, a profile of sensors was inserted in the snowpack, and undisturbed measurements of liquid water content were obtained using time-domain-reflectometry based devices. To assist in the interpretation of the readings from these sensors, some laboratory tests were run, and a FEM model of a sensor was implemented. Results show that sensors are sensitive to increasing liquid water content in snow. Nonetheless, long-term tests in snow cause the systematic development of an air gap between the instrument and the surrounding snow, that hampers the interpretation. Perspectives on future investigation are discussed to bring the proposed procedure towards long-term applications in snowpacks.

  13. Method for determination of radon-222 in water by liquid scintillation counting

    International Nuclear Information System (INIS)

    Suomela, J.

    1993-06-01

    The procedure for the determination of radon-222 by liquid scintillation counting is quite specific for this radionuclide. Radon-222 is extracted readily from the water sample by an organic scintillant. The decay products of radon-222 will remain in the water phase whilst radon-222 will be extracted into the organic phase. Before measurement the sample is stored for three hours until equilibrium is reached between radon-222 and its alpha emitting decay products. The alpha activity from radon-222 and its decay products is measured in a liquid scintillation counter

  14. Pressure evolution of the high-frequency sound velocity in liquid water

    International Nuclear Information System (INIS)

    Krisch, M.; Sette, F.; D'Astuto, M.; Lorenzen, M.; Mermet, A.; Monaco, G.; Verbeni, R.; Loubeyre, P.; Le Toullec, R.; Ruocco, G.; Cunsolo, A.

    2002-01-01

    The high-frequency sound velocity v ∞ of liquid water has been determined to densities of 1.37 g/cm 3 by inelastic x-ray scattering. In comparison to the hydrodynamic sound velocity v 0 , the increase of v ∞ with density is substantially less pronounced, indicating that, at high density, the hydrogen-bond network is decreasingly relevant to the physical properties of liquid water. Furthermore, we observe an anomaly in v ∞ at densities around 1.12 g/cm 3 , contrasting the smooth density evolution of v 0

  15. Vapor-Liquid Equilibrium Measurements and Modeling of the Propyl Mercaptan plus Methane plus Water System

    DEFF Research Database (Denmark)

    Awan, Javeed; Thomsen, Kaj; Coquelet, Christophe

    2010-01-01

    In this work, vapor−liquid equilibrium (VLE) measurements of propyl mercaptan (PM) in pure water were performed at three different temperatures, (303, 323, and 365) K, with a pressure variation from (1 to 8) MPa. The total system pressure was maintained by CH4. The inlet mole fraction of propyl...... mercaptan in all experiments was the same, around 4.5·10−4 in the liquid phase. The objective was to provide experimental VLE data points of the propyl mercaptan + methane + water system for modeling since there is a lack of available data. These data will allow the industrial modeling of sulfur emission...

  16. Determinations of cloud liquid water in the tropics from the SSM/I

    Science.gov (United States)

    Alishouse, John C.; Swift, Calvin; Ruf, Christopher; Snyder, Sheila; Vongsathorn, Jennifer

    1989-01-01

    Upward-looking microwave radiometric observations were used to validate the SSM/I determinations, and also as a basis for the determination of new coefficients. Due to insufficiency of the initial four channel algorithm for cloud liquid water, the improved algorithm was derived from the CORRAD (the University of Massachusetts autocorrelation radiometer) measurements of cloud liquid water and the matching SSM/I brightness temperatures using the standard linear regression. The correlation coefficients for the possible four channel combinations, and subsequently the best and the worst combinations were determined.

  17. Experimental determination of cavitation thresholds in liquid water and mercury

    International Nuclear Information System (INIS)

    Taleyarkhan, R.P.; West, C.D.; Moraga, F.

    1998-01-01

    An overview is provided on cavitation threshold measurement experiments for water and mercury. Various aspects to be considered that affect onset determination are discussed along with design specifications developed for construction of appropriate apparatus types. Both static and transient-cavitation effects were studied using radically different apparatus designs. Preliminary data are presented for cavitation thresholds for water and mercury over a range of temperatures in static and high-frequency environments. Implications and issues related to spallation neutron source target designs and operation are discussed

  18. Optimization and validation of liquid-liquid extraction with low temperature partitioning for determination of carbamates in water.

    Science.gov (United States)

    Goulart, Simone Machado; Alves, Renata Domingos; Neves, Antônio Augusto; de Queiroz, José Humberto; de Assis, Tamires Condé; de Queiroz, Maria Eliana L R

    2010-06-25

    Using a 2(3) experimental design, liquid-liquid extraction with low temperature partitioning (LLE-LTP) was optimized and validated for analysis of three carbamates (aldicarb, carbofuran and carbaryl) in water samples. In this method, 2.0 mL of sample is placed in contact with 4.0 mL of acetonitrile. After agitation, the sample is placed in a freezer for 3 h for phase separation. The organic extract is analyzed by high performance liquid chromatography with ultraviolet detection (HPLC-UV). For validation of the technique, the following figures of merit were evaluated: accuracy, precision, detection and quantification limits, linearity, sensibility and selectivity. Extraction recovery percentages of the carbamates aldicarb, carbofuran and carbaryl were 90%, 95% and 96%, respectively. Even though extremely low volumes of sample and solvent were used, the extraction method was selective and the detection and quantification limits were between 5.0 and 10.0 microg L(-1), and 17.0 and 33.0 microg L(-1), respectively. Copyright 2010 Elsevier B.V. All rights reserved.

  19. Short-range precipitation forecasts using assimilation of simulated satellite water vapor profiles and column cloud liquid water amounts

    Science.gov (United States)

    Wu, Xiaohua; Diak, George R.; Hayden, Cristopher M.; Young, John A.

    1995-01-01

    These observing system simulation experiments investigate the assimilation of satellite-observed water vapor and cloud liquid water data in the initialization of a limited-area primitive equations model with the goal of improving short-range precipitation forecasts. The assimilation procedure presented includes two aspects: specification of an initial cloud liquid water vertical distribution and diabatic initialization. The satellite data is simulated for the next generation of polar-orbiting satellite instruments, the Advanced Microwave Sounding Unit (AMSU) and the High-Resolution Infrared Sounder (HIRS), which are scheduled to be launched on the NOAA-K satellite in the mid-1990s. Based on cloud-top height and total column cloud liquid water amounts simulated for satellite data a diagnostic method is used to specify an initial cloud water vertical distribution and to modify the initial moisture distribution in cloudy areas. Using a diabatic initialization procedure, the associated latent heating profiles are directly assimilated into the numerical model. The initial heating is estimated by time averaging the latent heat release from convective and large-scale condensation during the early forecast stage after insertion of satellite-observed temperature, water vapor, and cloud water formation. The assimilation of satellite-observed moisture and cloud water, together withy three-mode diabatic initialization, significantly alleviates the model precipitation spinup problem, especially in the first 3 h of the forecast. Experimental forecasts indicate that the impact of satellite-observed temperature and water vapor profiles and cloud water alone in the initialization procedure shortens the spinup time for precipitation rates by 1-2 h and for regeneration of the areal coverage by 3 h. The diabatic initialization further reduces the precipitation spinup time (compared to adiabatic initialization) by 1 h.

  20. (Liquid + liquid) equilibrium data for the system (propylene glycol + water + tetraoctyl ammonium 2-methyl-1-naphthoate)

    NARCIS (Netherlands)

    Garcia Chavez, L.Y.; Shazad, M.; Schuur, Boelo; de Haan, A.B.

    2012-01-01

    Propylene glycol (PG) is an important low toxic glycol, widely used in the food, cosmetics, pharmaceutical and the chemical industries. The recovery of PG from aqueous streams using conventional unit operations such as evaporation is highly energy demanding because of the large amounts of water that

  1. On the existence and stability of liquid water on the surface of mars today

    Science.gov (United States)

    Kuznetz, L. H.; Gan, D. C.

    2002-01-01

    The recent discovery of high concentrations of hydrogen just below the surface of Mars' polar regions by Mars Odyssey has enlivened the debate about past or present life on Mars. The prevailing assumption prior to the discovery was that the liquid water essential for its existence is absent. That assumption was based largely on the calculation of heat and mass transfer coefficients or theoretical climate models. This research uses an experimental approach to determine the feasibility of liquid water under martian conditions, setting the stage for a more empirical approach to the question of life on Mars. Experiments were conducted in three parts: Liquid water's existence was confirmed by droplets observed under martian conditions in part 1; the evolution of frost melting on the surface of various rocks under martian conditions was observed in part 2; and the evaporation rate of water in Petri dishes under Mars-like conditions was determined and compared with the theoretical predictions of various investigators in part 3. The results led to the conclusion that liquid water can be stable for extended periods of time on the martian surface under present-day conditions.

  2. In situ metathesis ionic liquid formation dispersive liquid-liquid microextraction for copper determination in water samples by electrothermal atomic absorption spectrometry.

    Science.gov (United States)

    Stanisz, Ewa; Zgoła-Grześkowiak, Agnieszka

    2013-10-15

    In situ synthesis of ionic liquid extractant for dispersive liquid-liquid microextraction (in situ IL DLLME) combined with electrothermal atomic absorption spectrometry (ET AAS) for determination of copper in water samples was developed. Analytical signals were obtained without the back-extraction of copper from the IL phase prior to its determination by AAS. Some essential parameters of the microextraction and detection techniques such as the pH of sample solution, volume of components for in situ synthesis, matrix interferences and main parameters of graphite furnace atomizer have been studied. Under optimal conditions, high extraction efficiency for copper was achieved for the extraction of 0.7 µg L(-1) in 10.0 mL of sample solution employing 8 μL of 1-hexyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide (HmimNTf2) as the extraction solvent. The detection limit was found as 0.004 µg L(-1) with an enrichment factor of 200. The relative standard deviation (RSD) for seven replicate measurements of 0.7 µg L(-1) in sample solution was 4%. The accuracy of the proposed method was evaluated by analysis of the Certified Reference Materials: NIST SRM 2709 (San Joaquin Soil), NBS SRM 2704 (Buffalo River Sediment), NRCC DOLT-2 (Dogfish Liver) and NIST SRM 1643e (Trace Element in Water). The measured copper contents in the reference materials were in satisfactory agreement with the certified values. The method was successfully applied to analysis of the tap, lake and mineral water samples. © 2013 Elsevier B.V. All rights reserved.

  3. Water-free rare-earth-metal ionic liquids/ionic liquid crystals based on hexanitratolanthanate(III) anion.

    Science.gov (United States)

    Ji, Shun-Ping; Tang, Meng; He, Ling; Tao, Guo-Hong

    2013-04-02

    The hexanitratolanthanate anion (La(NO(3))(6)(3-)) is an interesting symmetric anion suitable to construct the component of water-free rare-earth-metal ionic liquids. The syntheses and structural characterization of eleven lanthanum nitrate complexes, [C(n)mim](3)[La(NO(3))(6)] (n=1, 2, 4, 6, 8, 12, 14, 16, 18), including 1,3-dimethylimidazolium hexanitratolanthanate ([C(1)mim](3)[La(NO(3))(6)], 1), 1-ethyl-3-methylimidazolium hexanitratolanthanate ([C(2)mim](3)[La(NO(3))(6)], 2), 1-butyl-3-methylimidazolium hexanitratolanthanate ([C(4)mim](3)[La(NO(3))(6)], 3), 1-isobutyl-3-methylimidazolium hexanetratolanthanate ([isoC(4)mim](3)[La(NO(3))(6)], 4), 1-methyl-3-(3'-methylbutyl)imidazolium hexanitratolanthanate ([MC(4)mim](3)[La(NO(3))(6)], 5), 1-hexyl-3-methylimidazolium hexanitratolanthanate ([C(6)mim](3)[La(NO(3))(6)], 6), 1-methyl-3-octylimidazolium hexanitratolanthanate ([C(8)mim](3)[La(NO(3))(6)], 7), 1-dodecyl-3-methylimidazolium hexanitratolanthanate ([C(12)mim](3)[La(NO(3))(6)], 8), 1-methyl-3-tetradecylimidazolium hexanitratolanthanate ([C(14)mim](3)[La-(NO(3))(6)], 9), 1-hexadecyl-3-methylimid-azolium hexanitratolanthanum ([C(16)dmim](3)[La(NO(3))(6)], 10), and 1-methyl-3-octadecylimidazolium hexanitratolanthanate ([C(18)mim](3)[La(NO(3))(6)], 11) are reported. All new compounds were characterized by (1)H and (13)C NMR, and IR spectroscopy as well as elemental analysis. The crystal structure of compound 1 was determined by using single-crystal X-ray diffraction, giving the following crystallographic information: monoclinic; P2(1)/c; a=15.3170 (3), b=14.2340 (2), c=13.8954(2) Å; β=94.3453(15)°, V=3020.80(9) Å(3), Z=4, ρ=1.764 g cm(-3). The coordination polyhedron around the lanthanum ion is rationalized by six nitrate anions with twelve oxygen atoms. No hydrogen-bonding network or water molecule was found in 1. The thermodynamic stability of the new complexes was investigated by using thermogravimetric analysis (TGA). The water

  4. Automated high performance liquid chromatography and liquid scintillation counting determination of pesticide mixture octanol/water partition rates

    International Nuclear Information System (INIS)

    Moody, R.P.; Carroll, J.M.; Kresta, A.M.

    1987-01-01

    Two novel methods are reported for measuring octanol/water partition rates of pesticides. A liquid scintillation counting (LSC) method was developed for automated monitoring of 14 C-labeled pesticides partitioning in biphasic water/octanol cocktail systems with limited success. A high performance liquid chromatography (HPLC) method was developed for automated partition rate monitoring of several constituents in a pesticide mixture, simultaneously. The mean log Kow +/- SD determined from triplicate experimental runs were for: 2,4-D-DMA (2,4-dichlorophenoxyacetic acid dimethylamine), 0.65 +/- .17; Deet (N,N-diethyl-m-toluamide), 2.02 +/- .01; Guthion (O,O-dimethyl-S-(4-oxo-1,2,3-benzotriazin-3(4H)-ylmethyl) phosphorodithioate), 2.43 +/- .03; Methyl-Parathion (O,O-dimethyl-O-(p-nitrophenyl) phosphorothioate), 2.68 +/- .05; and Fenitrothion (O,O-dimethyl O-(4-nitro-m-tolyl) phosphorothioate), 3.16 +/- .03. A strong positive linear correlation (r = .9979) was obtained between log Kow and log k' (log Kow = 2.35 (log k') + 0.63). The advantages that this automated procedure has in comparison with the standard manual shake-flask procedure are discussed

  5. Effect of simple solutes on the long range dipolar correlations in liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Baul, Upayan, E-mail: upayanb@imsc.res.in; Anishetty, Ramesh, E-mail: ramesha@imsc.res.in; Vemparala, Satyavani, E-mail: vani@imsc.res.in [The Institute of Mathematical Sciences, C.I.T. Campus, Taramani, Chennai 600113 (India); Kanth, J. Maruthi Pradeep, E-mail: jmpkanth@gmail.com [Vectra LLC, Mount Road, Chennai 600006 (India)

    2016-03-14

    Intermolecular correlations in liquid water at ambient conditions have generally been characterized through short range density fluctuations described through the atomic pair distribution functions. Recent numerical and experimental results have suggested that such a description of order or structure in liquid water is incomplete and there exist considerably longer ranged orientational correlations in water that can be studied through dipolar correlations. In this study, using large scale classical, atomistic molecular dynamics simulations using TIP4P-Ew and TIP3P models of water, we show that salts such as sodium chloride (NaCl), potassium chloride (KCl), caesium chloride (CsCl), and magnesium chloride (MgCl{sub 2}) have a long range effect on the dipolar correlations, which cannot be explained by the notion of structure making and breaking by dissolved ions. Observed effects are explained through orientational stratification of water molecules around ions and their long range coupling to the global hydrogen bond network by virtue of the sum rule for water. The observations for single hydrophilic solutes are contrasted with the same for a single methane (CH{sub 4}) molecule. We observe that even a single small hydrophobe can result in enhancement of long range orientational correlations in liquid water, contrary to the case of dissolved ions, which have been observed to have a reducing effect. The observations from this study are discussed in the context of hydrophobic effect.

  6. Phase equilibria of didecyldimethylammonium nitrate ionic liquid with water and organic solvents

    International Nuclear Information System (INIS)

    Domanska, Urszula; Lugowska, Katarzyna; Pernak, Juliusz

    2007-01-01

    The phase diagrams for binary mixtures of an ammonium ionic liquid, didecyldimethylammonium nitrate, [DDA][NO 3 ], with: alcohols (propan-1-ol, butan-1-ol, octan-1-ol, and decan-1-ol): hydrocarbons (toluene, propylbenzene, hexane, and hexadecane) and with water were determined in our laboratory. The phase equilibria were measured by a dynamic method from T 220 K to either the melting point of the ionic liquid, or to the boiling point of the solvent. A simple liquidus curve in a eutectic system was observed for [DDA][NO 3 ] with: alcohols (propan-1-ol, butan-1-ol, and octan-1-ol); aromatic hydrocarbons (toluene and propylbenzene) and with water. (Solid + liquid) equilibria with immiscibility in the liquid phase were detected with the aliphatic hydrocarbons heptane and hexadecane and with decan-1-ol. (Liquid + liquid) equilibria for the system [DDA][NO 3 ] with hexadecane was observed for the whole mole fraction range of the ionic liquid. The observation of the upper critical solution temperature in binary mixtures of ([DDA][NO 3 ] + decan-1-ol, heptane, or hexadecane) was limited by the boiling temperature of the solvent. Characterisation and purity of the compounds were determined by elemental analysis, water content (Fisher method) and differential scanning microcalorimetry (d.s.c.) analysis. The d.s.c. method of analysis was used to determine melting temperatures and enthalpies of fusion. The thermal stability of the ionic liquid was resolved by the thermogravimetric technique-differential thermal analysis (TG-DTA) technique over a wide temperature range from (200 to 780) K. The thermal decomposition temperature of 50% of the sample was greater than 500 K. The (solid + liquid) phase equilibria, curves were correlated by means of different G Ex models utilizing parameters derived from the (solid + liquid) equilibrium. The root-mean-square deviations of the solubility temperatures for all calculated data are dependent upon the particular system and the particular

  7. Phase equilibria of didecyldimethylammonium nitrate ionic liquid with water and organic solvents

    Energy Technology Data Exchange (ETDEWEB)

    Domanska, Urszula [Physical Chemistry Division, Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warsaw (Poland)]. E-mail: ula@ch.pw.edu.pl; Lugowska, Katarzyna [Physical Chemistry Division, Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warsaw (Poland); Pernak, Juliusz [Faculty of Chemical Technology, Poznan University of Technology, Poznan (Poland)

    2007-05-15

    The phase diagrams for binary mixtures of an ammonium ionic liquid, didecyldimethylammonium nitrate, [DDA][NO{sub 3}], with: alcohols (propan-1-ol, butan-1-ol, octan-1-ol, and decan-1-ol): hydrocarbons (toluene, propylbenzene, hexane, and hexadecane) and with water were determined in our laboratory. The phase equilibria were measured by a dynamic method from T 220 K to either the melting point of the ionic liquid, or to the boiling point of the solvent. A simple liquidus curve in a eutectic system was observed for [DDA][NO{sub 3}] with: alcohols (propan-1-ol, butan-1-ol, and octan-1-ol); aromatic hydrocarbons (toluene and propylbenzene) and with water. (Solid + liquid) equilibria with immiscibility in the liquid phase were detected with the aliphatic hydrocarbons heptane and hexadecane and with decan-1-ol. (Liquid + liquid) equilibria for the system [DDA][NO{sub 3}] with hexadecane was observed for the whole mole fraction range of the ionic liquid. The observation of the upper critical solution temperature in binary mixtures of ([DDA][NO{sub 3}] + decan-1-ol, heptane, or hexadecane) was limited by the boiling temperature of the solvent. Characterisation and purity of the compounds were determined by elemental analysis, water content (Fisher method) and differential scanning microcalorimetry (d.s.c.) analysis. The d.s.c. method of analysis was used to determine melting temperatures and enthalpies of fusion. The thermal stability of the ionic liquid was resolved by the thermogravimetric technique-differential thermal analysis (TG-DTA) technique over a wide temperature range from (200 to 780) K. The thermal decomposition temperature of 50% of the sample was greater than 500 K. The (solid + liquid) phase equilibria, curves were correlated by means of different G {sup Ex} models utilizing parameters derived from the (solid + liquid) equilibrium. The root-mean-square deviations of the solubility temperatures for all calculated data are dependent upon the particular

  8. Growth of volcanic ash aggregates in the presence of liquid water and ice: an experimental approach

    Science.gov (United States)

    Van Eaton, Alexa R.; Muirhead, James D.; Wilson, Colin J. N.; Cimarelli, Corrado

    2012-11-01

    Key processes influencing the aggregation of volcanic ash and hydrometeors are examined with an experimental method employing vibratory pan aggregation. Mechanisms of aggregation in the presence of hail and ice pellets, liquid water (≤30 wt%), and mixed water phases are investigated at temperatures of 18 and -20 °C. The experimentally generated aggregates, examined in hand sample, impregnated thin sections, SEM imagery, and X-ray microtomography, closely match natural examples from phreatomagmatic phases of the 27 ka Oruanui and 2010 Eyjafjallajökull eruptions. Laser diffraction particle size analysis of parent ash and aggregates is also used to calculate the first experimentally derived aggregation coefficients that account for changing liquid water contents and subzero temperatures. These indicate that dry conditions (collection of sub-63 μm particles into aggregates (given by aggregation coefficients >1). In contrast, liquid-saturated conditions (>15-20 wt% liquid) promote less size selective processes. Crystalline ice was also capable of preferentially selecting volcanic ash center of natural aggregates was also replicated during interaction of ash and melting ice pellets, followed by sublimation. Fine-grained rims were formed by adding moist aggregates to a dry mixture of sub-31 μm ash, which adhered by electrostatic forces and sparse liquid bridges. From this, we infer that the fine-grained outer layers of natural aggregates reflect recycled exposure of moist aggregates to regions of volcanic clouds that are relatively dry and dominated by <31 μm ash.

  9. Laser-based diagnostics for the measurement of liquid water film thickness.

    Science.gov (United States)

    Greszik, Daniel; Yang, Huinan; Dreier, Thomas; Schulz, Christof

    2011-02-01

    Three different diagnostic techniques are investigated for measurement of the thickness of liquid water films deposited on a transparent quartz plate. The methods are based on laser-induced fluorescence (LIF) from low concentrations of a dissolved tracer substance and spontaneous Raman scattering of liquid water, respectively, both excited with 266 nm of radiation, and diode laser absorption spectroscopy (DLAS) in the near-infrared spectral region. Signal intensities are calibrated using liquid layers of known thickness between 0 and 1000 μm. When applied to evaporating liquid water films, the thickness values derived from the direct DLAS and Raman scattering measurements correlate well with each other as a function of time after the start of data recording, while the LIF signal derived thickness values decrease faster with time due to selective tracer evaporation from the liquid. The simultaneous application of the LIF with a tracer-free detection technique can serve as an in situ reference for quantitative film thickness measurements.

  10. Vapor-liquid equilibria of the water + 1,3-propanediol and water + 1,3-propanediol + lithium bromide systems

    Energy Technology Data Exchange (ETDEWEB)

    Mun, S.Y.; Lee, H.

    1999-12-01

    Vapor-liquid equilibrium data of the water + 1,3-propanediol and water + 1,3-propanediol + lithium bromide systems were measured at 60, 160, 300, and 760 mmHg at temperatures ranging from 315 to 488 K. The apparatus used in this work is a modified still especially designed for the measurement of low-pressure VLE, in which both liquid and vapor are continuously recirculated. For the analysis of salt-containing solutions, a method incorporating refractometry and gravimetry was used. From the experimental measurements, the effect of lithium bromide on the VLE behavior of water + 1,3-propanediol was investigated. The experimental data of the salt-free system were successfully correlated using the Wilson, NRTL, and UNIQUAC models. In addition, the extended UNIQUAC model of Sander et al. was applied to the VLE calculation of salt-containing mixtures.

  11. Visual observation of gas hydrates nucleation and growth at a water - organic liquid interface

    Science.gov (United States)

    Stoporev, Andrey S.; Semenov, Anton P.; Medvedev, Vladimir I.; Sizikov, Artem A.; Gushchin, Pavel A.; Vinokurov, Vladimir A.; Manakov, Andrey Yu.

    2018-03-01

    Visual observation of nucleation sites of methane and methane-ethane-propane hydrates and their further growth in water - organic liquid - gas systems with/without surfactants was carried out. Sapphire Rocking Cell RCS6 with transparent sapphire cells was used. The experiments were conducted at the supercooling ΔTsub = 20.2 °C. Decane, toluene and crude oils were used as organics. Gas hydrate nucleation occurred on water - metal - gas and water - sapphire - organic liquid three-phase contact lines. At the initial stage of growth hydrate crystals rapidly covered the water - gas or water - organics interfaces (depending on the nucleation site). Further hydrate phase accrete on cell walls (sapphire surface) and into the organics volume. At this stage, growth was accompanied by water «drawing out» from under initial hydrate film formed at water - organic interface. Apparently, it takes place due to water capillary inflow in the reaction zone. It was shown that the hydrate crystal morphology depends on the organic phase composition. In the case of water-in-decane emulsion relay hydrate crystallization was observed in the whole sample, originating most likely due to the hydrate crystal intergrowth through decane. Contacts of such crystals with adjacent water droplets result in rapid hydrate crystallization on this droplet.

  12. Structure and dynamics in liquid water from x-ray absorption spectroscopy

    International Nuclear Information System (INIS)

    Wernet, Philippe

    2009-01-01

    Oxygen K-edge x-ray absorption spectra of water are discussed. The spectra of gas-phase water, liquid water and ice illustrate the sensitivity of oxygen K-edge x-ray absorption spectroscopy to hydrogen bonding in water. Transmission mode spectra of amorphous and crystalline ice are compared to x-ray Raman spectra of ice. The good agreement consolidates the experimental spectrum of crystalline ice and represents an incentive for theoretical calculations of the oxygen K-edge absorption spectrum of crystalline ice. Time-resolved infrared-pump and x-ray absorption probe results are finally discussed in the light of this structural interpretation.

  13. Evidence of a reduction in cloud condensation nuclei activity of water-soluble aerosols caused by biogenic emissions in a cool-temperate forest.

    Science.gov (United States)

    Müller, Astrid; Miyazaki, Yuzo; Tachibana, Eri; Kawamura, Kimitaka; Hiura, Tsutom

    2017-08-16

    Biogenic organic aerosols can affect cloud condensation nuclei (CCN) properties, and subsequently impact climate change. Large uncertainties exist in how the difference in the types of terrestrial biogenic sources and the abundance of organics relative to sulfate affect CCN properties. For the submicron water-soluble aerosols collected for two years in a cool-temperate forest in northern Japan, we show that the hygroscopicity parameter κ CCN (0.44 ± 0.07) exhibited a distinct seasonal trend with a minimum in autumn (κ CCN  = 0.32-0.37); these κ CCN values were generally larger than that of ambient particles, including water-insoluble fractions. The temporal variability of κ CCN was controlled by the water-soluble organic matter (WSOM)-to-sulfate ratio (R 2  > 0.60), where the significant reduction of κ CCN in autumn was linked to the increased WSOM/sulfate ratio. Positive matrix factorization analysis indicates that α-pinene-derived secondary organic aerosol (SOA) substantially contributed to the WSOM mass (~75%) in autumn, the majority of which was attributable to emissions from litter/soil microbial activity near the forest floor. These findings suggest that WSOM, most likely α-pinene SOA, originated from the forest floor can significantly suppress the aerosol CCN activity in cool-temperate forests, which have implications for predicting climate effects by changes in biogenic emissions in future.

  14. Mars Gully: No Mineral Trace of Liquid Water

    Science.gov (United States)

    2007-01-01

    This image of the Centauri-Hellas Montes region was taken by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) at 2107 UTC (4:07 p.m. EST) on Jan. 9, 2007, near 38.41 degrees south latitude, 96.81 degrees east longitude. CRISM's image was taken in 544 colors covering 0.36-3.92 micrometers, and shows features as small as 20 meters (66 feet) across. The region covered is slightly wider than 10 kilometers (6.2 miles) at its narrowest point. Narrow gullies found on hills and crater walls in many mid-latitude regions of Mars have been interpreted previously as cut by geologically 'recent' running water, meaning water that flowed on Mars long after impact cratering, tectonic forces, volcanism or other processes created the underlying landforms. Some gullies even eroded into sand dunes, which would date their formation at thousands to millions of years ago, or less. In fact, Mars Orbiter Camera (MOC) images showed two of the gullies have bright deposits near their downslope ends - but those deposits were absent in images taken just a few years earlier. The bright deposits must have formed within the period 1999-2004. Has there been running water on Mars so recently? To address that question, CRISM and MRO's other instruments observed the bright gully deposits. CRISM's objective was to determine if the bright deposits contained salts left behind from water evaporating into Mars' thin air. The high-resolution imager's (HiRISE's) objective was to determine if the small-scale morphology was consistent with formation by running water. This CRISM image of a bright gully deposit was constructed by showing 2.53, 1.50, and 1.08 micrometer light in the red, green, and blue image planes. CRISM can just resolve the deposits (highlighted by arrows in the inset), which are only a few tens of meters (about 150 feet) across. The spectrum of the deposits barely differs from that of the surrounding material, and is just a little brighter. This difference could simply be

  15. The supramolecular structure of liquid water and quantum coherent processes in biology

    International Nuclear Information System (INIS)

    Ninno, A De; Castellano, A Congiu; Giudice, E Del

    2013-01-01

    Vibrational spectroscopy provides a powerful tool to understand the molecular structures. When applied to the liquid water, this technique reveals so many details which can also shed a light on the supramolecular arrangement of the most ubiquitous of the substances. In particular, the two fluid model of water, proposed several decades ago, founds experimental evidence. Moreover, some fundamental parameters calculated in the realm of the theory of Quantum ElectroDynamics applied to liquid water can be actually measured showing an excellent agreement with the theory. This allows to add a dynamical origin to the mixed cluster model of water well known by the biologists for fifty years and opens the way to the dawn of a real quantum biology.

  16. An investigation of sulfate production in clouds using a flow-through chemical reactor model approach

    Science.gov (United States)

    Hong, M. S.; Carmichael, G. R.

    1983-01-01

    A flow-through chemical reactor model is developed to describe the mass transfer and chemical processes that atmospheric gases undergo in clouds. The model includes the simultaneous absorption of SO2, NH3, O3, NO(x), HNO3, CO2 and H2O2, the accompanying dissociation and oxidation reactions in cloud water, considers electrical neutrality, and includes qualitative parameterization of cloud microphysics. The model is used to assess the importance of the oxidation reactions H2O2-S(IV), O3-S(IV), and S(IV)-Mn(2+) catalysis, and the effects of cloud parameters such as drop size, rain intensity, liquid water content, and updraft velocity. Both precipitating and nonprecipitating clouds are studied. Model results predict sulfate production rates varying from 3 percent/hr to 230 percent/hr. The actual rate is highly dependent on the chemical composition of the uptake air and the physical conditions of the cloud. Model results also show that both the H2O2 and the O3 oxidation reactions can be significant.

  17. Sub- and super-Maxwellian evaporation of simple gases from liquid water

    International Nuclear Information System (INIS)

    Kann, Z. R.; Skinner, J. L.

    2016-01-01

    Non-Maxwellian evaporation of light atoms and molecules (particles) such as He and H 2 from liquids has been observed experimentally. In this work, we use simulations to study systematically the evaporation of Lennard-Jones particles from liquid water. We find instances of sub- and super-Maxwellian evaporation, depending on the mass of the particle and the particle-water interaction strength. The observed trends are in qualitative agreement with experiment. We interpret these trends in terms of the potential of mean force and the effectiveness and frequency of collisions during the evaporation process. The angular distribution of evaporating particles is also analyzed, and it is shown that trends in the energy from velocity components tangential and normal to the liquid surface must be understood separately in order to interpret properly the angular distributions.

  18. Changes of liquid Water content in fog at Milešovka Observatory (Czech Republic)

    Czech Academy of Sciences Publication Activity Database

    Fišák, Jaroslav

    2008-01-01

    Roč. 11, - (2008), s. 5-8 ISSN 1335-339X R&D Projects: GA AV ČR IAA3042301; GA AV ČR 1QS200420562 Institutional research plan: CEZ:AV0Z30420517 Keywords : fog * liquid water content * month changes * Observatory Milešovka * visibility Subject RIV: DG - Athmosphere Sciences, Meteorology

  19. Observed and simulated temperature dependence of the liquid water path of low clouds

    Energy Technology Data Exchange (ETDEWEB)

    Del Genio, A.D.; Wolf, A.B. [NASA Goddard Institute for Space Studies, New York, NY (United States)

    1996-04-01

    Data being acquired at the Atmospheric Radiation Measurement (ARM) Southern great Plains (SGP) Cloud and Radiation Testbed (CART) site can be used to examine the factors determining the temperature dependence of cloud optical thickness. We focus on cloud liquid water and physical thickness variations which can be derived from existing ARM measurements.

  20. Retrieval of liquid water cloud properties from ground-based remote sensing observations

    NARCIS (Netherlands)

    Knist, C.L.

    2014-01-01

    Accurate ground-based remotely sensed microphysical and optical properties of liquid water clouds are essential references to validate satellite-observed cloud properties and to improve cloud parameterizations in weather and climate models. This requires the evaluation of algorithms for retrieval of

  1. GENERIC, COMPONENT FAILURE DATA BASE FOR LIGHT WATER AND LIQUID SODIUM REACTOR PRAs

    Energy Technology Data Exchange (ETDEWEB)

    S. A. Eide; S. V. Chmielewski; T. D. Swantz

    1990-02-01

    A comprehensive generic component failure data base has been developed for light water and liquid sodium reactor probabilistic risk assessments (PRAs) . The Nuclear Computerized Library for Assessing Reactor Reliability (NUCLARR) and the Centralized Reliability Data Organization (CREDO) data bases were used to generate component failure rates . Using this approach, most of the failure rates are based on actual plant data rather than existing estimates .

  2. Sensitive determination of thallium species in drinking and natural water by ionic liquid-assisted ion-pairing liquid-liquid microextraction and inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Escudero, Leticia B; Wuilloud, Rodolfo G; Olsina, Roberto A

    2013-01-15

    A fast and simple method involving separation and determination of thallium (Tl) species, based on novel ionic liquid-assisted ion pairing dispersive liquid-liquid microextraction (DLLME) method, was developed. Initially, Tl(III) was selectively complexed with chloride ion to form [TlCl(4)](-) chlorocomplex. Subsequently, tetradecyl(trihexyl)phosphonium chloride ionic liquid (CYPHOS(®) IL 101) was used to form the ion-pair with [TlCl(4)](-) anion followed by extraction. The DLLME procedure was developed by dispersing 80 μL of carbon tetrachloride with 100 μL of ethanol added to the aqueous solution. After DLLME, the upper aqueous phase containing Tl(I) only was removed and analysed by inductively coupled plasma-mass spectrometry (ICP-MS). In contrast to Tl(III), Tl(I) species does not form neither stable nor anionic complexes with chloride ions and it was not extracted into the organic phase. Total Tl concentration was obtained by direct introduction of sample into ICP-MS instrument. The calibration graph for the analyte was linear with a correlation coefficient of 0.9989. Under optimal conditions, detection limit of Tl species was 0.4 ng L(-1). The relative standard deviation (n=10) at 1 ng mL(-1) Tl concentration level was 1.3% for Tl(I) and 1.5% for Tl(III). The method was successfully applied for fast speciation analysis of Tl at ultratrace levels in real water samples. Copyright © 2012 Elsevier B.V. All rights reserved.

  3. Ionic liquid-based zinc oxide nanofluid for vortex assisted liquid liquid microextraction of inorganic mercury in environmental waters prior to cold vapor atomic fluorescence spectroscopic detection.

    Science.gov (United States)

    Amde, Meseret; Liu, Jing-Fu; Tan, Zhi-Qiang; Bekana, Deribachew

    2016-01-01

    Zinc oxide nanofluid (ZnO-NF) based vortex assisted liquid liquid microextraction (ZnO-NF VA-LLME) was developed and employed in extraction of inorganic mercury (Hg(2+)) in environmental water samples, followed by cold vapor atomic fluorescence spectrometry (CV-AFS). Unlike other dispersive liquid liquid microextraction techniques, ZnO-NF VA-LLME is free of volatile organic solvents and dispersive solvent consumption. Analytical signals were obtained without back-extraction from the ZnO-NF phase prior to CV-AFS determination. Some essential parameters of the ZnO-NF VA-LLME and cold vapor generation such as composition and volume of the nanofluid, vortexing time, pH of the sample solution, amount of the chelating agent, ionic strength and matrix interferences have been studied. Under optimal conditions, efficient extraction of 1ng/mL of Hg(2+) in 10mL of sample solution was achieved using 50μL of ZnO-NF. The enrichment factor before dilution, detection limits and limits of quantification of the method were about 190, 0.019 and 0.064ng/mL, respectively. The intra and inter days relative standard deviations (n=8) were found to be 4.6% and 7.8%, respectively, at 1ng/mL spiking level. The accuracy of the current method was also evaluated by the analysis of certified reference materials, and the measured Hg(2+) concentration of GBW08603 (9.6ng/mL) and GBW(E)080392 (8.9ng/mL) agreed well with their certified value (10ng/mL). The method was applied to the analysis of Hg(2+) in effluent, influent, lake and river water samples, with recoveries in the range of 79.8-92.8% and 83.6-106.1% at 1ng/mL and 5ng/mL spiking levels, respectively. Overall, ZnO-NF VA-LLME is fast, simple, cost-effective and environmentally friendly and it can be employed for efficient enrichment of the analyte from various water samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  4. Liquid-liquid equilibrium of water + PEG 8000 + magnesium sulfate or sodium sulfate aqueous two-phase systems at 35°C: experimental determination and thermodynamic modeling

    Directory of Open Access Journals (Sweden)

    B. D. Castro

    2005-09-01

    Full Text Available Liquid-liquid extraction using aqueous two-phase systems is a highly efficient technique for separation and purification of biomolecules due to the mild properties of both liquid phases. Reliable data on the phase behavior of these systems are essential for the design and operation of new separation processes; several authors reported phase diagrams for polymer-polymer systems, but data on polymer-salt systems are still relatively scarce. In this work, experimental liquid-liquid equilibrium data on water + polyethylene glycol 8000 + magnesium sulfate and water + polyethylene glycol 8000 + sodium sulfate aqueous two-phase systems were obtained at 35°C. Both equilibrium phases were analyzed by lyophilization and ashing. Experimental results were correlated with a mass-fraction-based NRTL activity coefficient model. New interaction parameters were estimated with the Simplex method. The mean deviations between the experimental and calculated compositions in both equilibrium phases is about 2%.

  5. The Inferred Distribution of Liquid Water in Europa's Ice Shell: Implications for the Europa Lander Mission

    Science.gov (United States)

    Noviello, J. L.; Torrano, Z. A.; Rhoden, A.; Manga, M.

    2017-12-01

    A key objective of the Europa lander mission is to identify liquid water within 30 km of the lander (Europa Lander SDT report, 2017), to provide essential context with which to evaluate samples and enable assessment of Europa's overall habitability. To inform lander mission development, we utilize a model of surface feature formation that invokes liquid water within Europa's ice shell to map out the implied 3D distribution of liquid water and assess the likelihood of a lander to be within 30 km of liquid water given regional variability. Europa's surface displays a variety of microfeatures, also called lenticulae, including pits, domes, spots, and microchaos. A recent model by Manga and Michaut (2017) attributes these features to various stages in the thermal-mechanical evolution of liquid water intrusions (i.e. sills) within the ice shell, from sill emplacement to surface breaching (in the case of microchaos) to freezing of the sill. Pits are of particular interest because they appear only when liquid water is still present. Another key feature of the model is that the size of a microfeature at the surface is controlled by the depth of the sill. Hence, we can apply this model to regions of Europa that contain microfeatures to infer the size, depth, and spatial distribution of liquid water within the ice shell. We are creating a database of microfeatures that includes digitized, collated data from previous mapping efforts along with our own mapping study. We focus on images with 220 m/pixel resolution, which includes the regional mapping data sets. Analysis of a preliminary study area suggests that sills are typically located at depths of 2km or less from the surface. We will present analysis of the full database of microfeatures and the corresponding 3D distribution of sills implied by the model. Our preliminary analysis also shows that pits are clustered in some regions, consistent with previous results, although individual pits are also observed. We apply a

  6. The influence of water on the structural and transport properties of model ionic liquids.

    Science.gov (United States)

    Spohr, Heidrun V; Patey, G N

    2010-06-21

    Molecular dynamics simulations are used to investigate the influence of water on model ionic liquids. Several models, where the ions vary in size, and in the location of the charge with respect to the center of mass, are considered. Particular attention is focused on the variation in transport properties (diffusion coefficients, shear viscosity, and electrical conductivity) with water concentration. An effort is made to identify the underlying physical reasons for water's influence. The results for our model ionic liquids fall loosely into two categories, depending on the molecular characteristics of the constituent ions. If the ion size disparity is not too large (cation:anion diameter ratio water concentration. This agrees with what is commonly observed experimentally for room temperature ionic liquids (RTILs). For these systems, we do not find changes in the equilibrium structure that can account for the strong influence of water on the transport properties. Rather, by varying the molecular mass of water in our simulations, we demonstrate that the dominant effect of water can be dynamical in origin. In RTIL-water mixtures, the molecular mass of water is generally much less than that of the ions it replaces. These lighter water molecules tend to displace much heavier counterions from the ion coordination shells. This reduces caging and increases the diffusivity, which leads to higher conductivities and lower viscosities. For models with a larger ion size disparity (3:1), or in charge-off-center systems, where strong directional ion pairs are important in the pure ionic liquid, the behavior can be quite different. In these systems, the diffusion coefficients and electrical conductivity can still display conventional behavior and increase when water is added even though the reasons for this can be more complex than in the simpler cases noted above. However, in these systems the viscosity can increase, sometimes quite steeply, with increasing water concentration. We

  7. A Novel Liquid-Liquid Extraction for the Determination of Sertraline in Tap Water and Waste Water at Trace Levels by GC-MS.

    Science.gov (United States)

    Koçoğlu, Elif Seda; Bakırdere, Sezgin; Keyf, Seyfullah

    2017-09-01

    A simple, green and fast analytical method was developed for the determination of sertraline in tap and waste water samples at trace levels by using supportive liquid-liquid extraction with gas chromatography-mass spectrometry. Different parameters affecting extraction efficiency such as types and volumes of extraction and supporter solvents, extraction period, salt type and amount were optimized to get lower detection limits. Ethyl acetate was selected as optimum extraction solvent. In order to improve the precision, anthracene-D10 was used as an internal standard. The calibration plot of sertraline was linear from 1.0 to 1000 ng/mL with a correlation coefficient of 0.999. The limit of detection value under the optimum conditions was found to be 0.43 ng/mL. In real sample measurements, spiking experiments were performed to check the reliability of the method for these matrices. The spiking experiments yielded satisfactory recoveries of 91.19 ± 2.48%, 90.48 ± 5.19% and 95.46 ± 6.56% for 100, 250 and 500 ng/mL sertraline for tap water, and 85.80 ± 2.15% and 92.43 ± 4.02% for 250 and 500 ng/mL sertraline for waste water.

  8. Isobaric vapor-liquid equilibria for the extractive distillation of 2-propanol + water mixtures using 1-ethyl-3-methylimidazolium dicyanamide ionic liquid

    International Nuclear Information System (INIS)

    Orchillés, A. Vicent; Miguel, Pablo J.; González-Alfaro, Vicenta; Llopis, Francisco J.; Vercher, Ernesto; Martínez-Andreu, Antoni

    2017-01-01

    Highlights: • VLE of binary and ternary systems of 2-propanol, water and [emim][DCA] at 100 kPa. • The e-NRTL model fits the VLE data of 2-propanol + water + [emim][DCA] system. • [emim][DCA] breaks the 2-propanol + water azeotrope at an IL mole fraction >0.085. - Abstract: Isobaric vapor–liquid equilibria for the binary systems 2-propanol + water, 2-propanol + 1-ethyl-3-methylimidazolium dicyanamide ([emim][DCA]), and water + [emim][DCA] as well as the vapor–liquid equilibria for the 2-propanol + water + [emim][DCA] ternary system have been obtained at 100 kPa using a recirculating still. The electrolyte nonrandom two-liquid (e-NRTL) model was used for fitting successfully the experimental data. The effect of [emim][DCA] on the 2-propanol + water system has been compared with that produced by other ionic liquids reported in the literature. From the results, [emim][DCA] appears as a good entrainer for the extractive distillation of this solvent mixture, causing the azeotrope to disappear at 100 kPa when the ionic liquid mole fraction is greater than 0.085.

  9. Ionic liquid-based dispersive liquid-liquid microextraction combined with high performance liquid chromatography-UV detection for simultaneous preconcentration and determination of Ni, Co, Cu and Zn in water samples

    Directory of Open Access Journals (Sweden)

    Asghari Alireza

    2014-01-01

    Full Text Available Ionic liquid-based dispersive liquid-liquid microextraction (IL-DLLME coupled with high performance liquid chromatography (HPLC-UV detection was developed for simultaneous extraction and determination of nickel, cobalt, copper and zinc ions. In the proposed approach, salophen (N,N'-bis(salisyliden-1,2-phenylenediamine was used as a chelating agent; the ionic liquid, 1-hexeyl-3-methylimidazolium hexafluorophosphate, and acetone were selected as extracting and dispersive solvents, respectively. After extraction, phase separation was performed by centrifugation and the sedimented phase (ionic liquid was solubilized in acetonitrile and directly injected into the HPLC for subsequent analysis. Baseline separation of metal ion complexes was achieved on a RP-C18 column using a gradient elution of the mixtures of methanol-acetonitrile-water as the mobile phase at a flow rate of 1.0 mL min-1. The influence of variables such as sample pH, concentration of the chelating agent, amount of ionic liquid (extraction solvent, disperser solvent volume, extraction time, salt effect and centrifugation speed were studied and optimized. Under the optimum conditions, the enrichment factor of 222 was obtained. The detection limits for Ni, Co, Cu and Zn were 0.8, 1.6, 1.9 and 2.8 μg L−1, respectively. The relative standard deviations (RSDs were in the range of 3.6-5.0 % for all of the investigated metal ions. The proposed procedure was successfully applied to the determination of the studied metal ions in water samples.

  10. Initial evaluation of profiles of temperature, water vapor, and cloud liquid water from a new microwave profiling radiometer.

    Energy Technology Data Exchange (ETDEWEB)

    Liljegren, J. C.; Lesht, B. M.; Clothiaux, E. E.; Kato, S.

    2000-11-01

    To measure the vertical profiles of temperature and water vapor that are essential for modeling atmospheric processes, the Atmospheric Radiation Measurement (ARM) Program of the U. S. Department of Energy launches approximately 2600 radiosondes each year from its Southern Great Plains (SGP) facilities in Oklahoma and Kansas, USA. The annual cost of this effort exceeds $500,000 in materials and labor. Despite the expense, these soundings have a coarse temporal resolution and reporting interval compared with model time steps. In contrast, the radiation measurements used for model evaluations have temporal resolutions and reporting intervals of a few minutes at most. Conversely, radiosondes have a much higher vertical spatial resolution than most models can use. Modelers generally reduce the vertical resolution of the soundings by averaging over the vertical layers of the model. Recently, Radiometries Corporation (Boulder, Colorado, USA) developed a 12-channel, ground-based microwave radiometer capable of providing continuous, real-time vertical profiles of temperature, water vapor, and limited-resolution cloud liquid water from the surface to 10 km in nearly all weather conditions. The microwave radiometer profiler (MWRP) offers a much finer temporal resolution and reporting interval (about 10 minutes) than the radiosonde but a coarser vertical resolution that may be more appropriate for models. Profiles of temperature, water vapor, and cloud liquid water are obtained at 47 levels: from 0 to 1 km above ground level at 100-m intervals and from 1 to 10 km at 250-m intervals. The profiles are derived from the measured brightness temperatures with neural network retrieval. In Figure 1, profiles of temperature, water vapor, and cloud liquid water for 10 May 2000 are presented as time-height plots. MWRP profiles coincident with the 11:31 UTC (05:31 local) and 23:47 UTC (17:47 local) soundings for 10 May are presented in Figures 2 and 3, respectively. These profiles

  11. Combined retrieval of Arctic liquid water cloud and surface snow properties using airborne spectral solar remote sensing

    Science.gov (United States)

    Ehrlich, André; Bierwirth, Eike; Istomina, Larysa; Wendisch, Manfred

    2017-09-01

    , C, and reff, S show a continuous transition of cloud properties across snow-covered sea ice and open water and are consistent with estimates based on satellite data. It is shown that the uncertainties of the trispectral retrieval increase for high values of τ, and low reff, S but nevertheless allow the effective snow grain size in cloud-covered areas to be estimated.

  12. Combined retrieval of Arctic liquid water cloud and surface snow properties using airborne spectral solar remote sensing

    Directory of Open Access Journals (Sweden)

    A. Ehrlich

    2017-09-01

    edge are analysed. The retrieved values of τ, reff, C, and reff, S show a continuous transition of cloud properties across snow-covered sea ice and open water and are consistent with estimates based on satellite data. It is shown that the uncertainties of the trispectral retrieval increase for high values of τ, and low reff, S but nevertheless allow the effective snow grain size in cloud-covered areas to be estimated.

  13. Numerical Investigation of a Liquid-Gas Ejector Used for Shipping Ballast Water Treatment

    Directory of Open Access Journals (Sweden)

    Xueguan Song

    2014-01-01

    Full Text Available Shipping ballast water can have significant ecological and economic impacts on aquatic ecosystems. Currently, water ejectors are widely used in marine applications for ballast water treatment owing to their high suction capability and reliability. In this communication, an improved ballast treatment system employing a liquid-gas ejector is introduced to clear the ballast water to reduce environmental risks. Commonly, the liquid-gas ejector uses ballast water as the primary fluid and chemical ozone as the secondary fluid. In this study, high-pressure water and air, instead of ballast water and ozone, are considered through extensive numerical and experimental research. The ejector is particularly studied by a steady three-dimensional multiphase computational fluid dynamics (CFD analysis with commercial software ANSYS-CFX 14.5. Different turbulence models (including standard k-ε, RNG k-ε, SST, and k-ω with different grid size and bubble size are compared extensively and the experiments are carried out to validate the numerical design and optimization. This study concludes that the RNG k-ε turbulence model is the most efficient and effective for the ballast water treatment system under consideration and simple change of nozzle shape can greatly improve the ejector performance under high back pressure conditions.

  14. Dissolved organic carbon (DOC and select aldehydes in cloud and fog water: the role of the aqueous phase in impacting trace gas budgets

    Directory of Open Access Journals (Sweden)

    B. Ervens

    2013-05-01

    Full Text Available Cloud and fog droplets efficiently scavenge and process water-soluble compounds and, thus, modify the chemical composition of the gas and particle phases. The concentrations of dissolved organic carbon (DOC in the aqueous phase reach concentrations on the order of ~ 10 mgC L−1 which is typically on the same order of magnitude as the sum of inorganic anions. Aldehydes and carboxylic acids typically comprise a large fraction of DOC because of their high solubility. The dissolution of species in the aqueous phase can lead to (i the removal of species from the gas phase preventing their processing by gas phase reactions (e.g., photolysis of aldehydes and (ii the formation of unique products that do not have any efficient gas phase sources (e.g., dicarboxylic acids. We present measurements of DOC and select aldehydes in fog water at high elevation and intercepted clouds at a biogenically-impacted location (Whistler, Canada and in fog water in a more polluted area (Davis, CA. Concentrations of formaldehyde, glyoxal and methylglyoxal were in the micromolar range and comprised ≤ 2% each individually of the DOC. Comparison of the DOC and aldehyde concentrations to those at other locations shows good agreement and reveals highest levels for both in anthropogenically impacted regions. Based on this overview, we conclude that the fraction of organic carbon (dissolved and insoluble inclusions in the aqueous phase of clouds or fogs, respectively, comprises 2–~ 40% of total organic carbon. Higher values are observed to be associated with aged air masses where organics are expected to be more highly oxidised and, thus, more soluble. Accordingly, the aqueous/gas partitioning ratio expressed here as an effective Henry's law constant for DOC (KH*DOC increases by an order of magnitude from 7 × 103 M atm−1 to 7 × 104 M atm−1 during the ageing of air masses. The measurements are accompanied by photochemical box model simulations. These simulations are

  15. Ab Initio Liquid Water Dynamics in Aqueous TMAO Solution.

    Science.gov (United States)

    Usui, Kota; Hunger, Johannes; Sulpizi, Marialore; Ohto, Tatsuhiko; Bonn, Mischa; Nagata, Yuki

    2015-08-20

    Ab initio molecular dynamics (AIMD) simulations in trimethylamine N-oxide (TMAO)-D2O solution are employed to elucidate the effects of TMAO on the reorientational dynamics of D2O molecules. By decomposing the O-D groups of the D2O molecules into specific subensembles, we reveal that water reorientational dynamics are retarded considerably in the vicinity of the hydrophilic TMAO oxygen (O(TMAO)) atom, due to the O-D···O(TMAO) hydrogen-bond. We find that this reorientational motion is governed by two distinct mechanisms: The O-D group rotates (1) after breaking the O-D···O(TMAO) hydrogen-bond, or (2) together with the TMAO molecule while keeping this hydrogen-bond intact. While the orientational slow-down is prominent in the AIMD simulation, simulations based on force field models exhibit much faster dynamics. The simulated angle-resolved radial distribution functions illustrate that the O-D···O(TMAO) hydrogen-bond has a strong directionality through the sp(3) orbital configuration in the AIMD simulation, and this directionality is not properly accounted for in the force field simulation. These results imply that care must be taken when modeling negatively charged oxygen atoms as single point charges; force field models may not adequately describe the hydration configuration and dynamics.

  16. Liquid Water Cloud Properties During the Polarimeter Definition Experiment (PODEX)

    Science.gov (United States)

    Alexandrov, Mikhail D.; Cairns, Brian; Wasilewski, Andrzei P.; Ackerman, Andrew S.; McGill, Matthew J.; Yorks, John E.; Hlavka, Dennis L.; Platnick, Steven; Arnold, George; Van Diedenhoven, Bastiaan; hide

    2015-01-01

    We present retrievals of water cloud properties from the measurements made by the Research Scanning Polarimeter (RSP) during the Polarimeter Definition Experiment (PODEX) held between January 14 and February 6, 2013. The RSP was onboard the high-altitude NASA ER-2 aircraft based at NASA Dryden Aircraft Operation Facility in Palmdale, California. The retrieved cloud characteristics include cloud optical thickness, effective radius and variance of cloud droplet size distribution derived using a parameter-fitting technique, as well as the complete droplet size distribution function obtained by means of Rainbow Fourier Transform. Multi-modal size distributions are decomposed into several modes and the respective effective radii and variances are computed. The methodology used to produce the retrieval dataset is illustrated on the examples of a marine stratocumulus deck off California coast and stratus/fog over California's Central Valley. In the latter case the observed bimodal droplet size distributions were attributed to two-layer cloud structure. All retrieval data are available online from NASA GISS website.

  17. A novel vortex-assisted liquid-liquid microextraction approach using auxiliary solvent: Determination of iodide in mineral water samples.

    Science.gov (United States)

    Zaruba, Serhii; Vishnikin, Andriy B; Andruch, Vasil

    2016-01-01

    A novel vortex-assisted liquid-liquid microextraction (VA-LLME) for determination of iodide was developed. The method includes the oxidation of iodide with iodate in the presence of hydrochloric acid followed by VA-LLME of the ion-pair formed between ICl2(-) and Astra Phloxine reagent (AP) and subsequent absorbance measurement at 555nm. The appropriate experimental conditions were investigated and found to be: 5mL of sample, 0.27molL(-)(1) HCl, 0.027mmolL(-1) KIO3 as the oxidation agent, 250μL of extraction mixture containing amyl acetate as the extraction solvent and carbon tetrachloride as the auxiliary solvent (1:1, v/v), 0.04mmolL(-1) AP reagent, vortex time: 20s at 3000rpm, centrifugation: 4min at 3000rpm. The calibration plot was linear in the range 16.9-169μg L(-1) of iodide, with a correlation coefficient (R(2)) of 0.996, and the relative standard deviation ranged from 1.9 to 5.7%. The limit of detection (LOD) and limit of quantification (LOQ) were 1.75 and 6.01μgL(-)(1) of iodide, respectively. The suggested procedure was applied for determination of iodide in real mineral water samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  18. Global simulations of aerosol processing in clouds

    Directory of Open Access Journals (Sweden)

    C. Hoose

    2008-12-01

    Full Text Available An explicit and detailed representation of in-droplet and in-crystal aerosol particles in stratiform clouds has been introduced in the global aerosol-climate model ECHAM5-HAM. The new scheme allows an evaluation of the cloud cycling of aerosols and an estimation of the relative contributions of nucleation and collision scavenging, as opposed to evaporation of hydrometeors in the global aerosol processing by clouds. On average an aerosol particle is cycled through stratiform clouds 0.5 times. The new scheme leads to important changes in the simulated fraction of aerosol scavenged in clouds, and consequently in the aerosol wet deposition. In general, less aerosol is scavenged into clouds with the new prognostic treatment than what is prescribed in standard ECHAM5-HAM. Aerosol concentrations, size distributions, scavenged fractions and cloud droplet concentrations are evaluated and compared to different observations. While the scavenged fraction and the aerosol number concentrations in the marine boundary layer are well represented in the new model, aerosol optical thickness, cloud droplet number concentrations in the marine boundary layer and the aerosol volume in the accumulation and coarse modes over the oceans are overestimated. Sensitivity studies suggest that a better representation of below-cloud scavenging, higher in-cloud collision coefficients, or a reduced water uptake by seasalt aerosols could reduce these biases.

  19. Polypropylene Nonwoven Fabric@Poly(ionic liquid)s for Switchable Oil/Water Separation, Dye Absorption, and Antibacterial Applications.

    Science.gov (United States)

    Ren, Yongyuan; Guo, Jiangna; Lu, Qian; Xu, Dan; Qin, Jing; Yan, Feng

    2018-03-22

    Pollutants in wastewater include oils, dyes, and bacteria, making wastewater cleanup difficult. Multifunctional wastewater treatment media consisting of poly(ionic liquid)-grafted polypropylene (PP) nonwoven fabrics (PP@PIL) are prepared by a simple and scalable surface-grafting process. The fabricated PP@PIL fabrics exhibit impressive switchable oil/water separation (η>99 %) and dye absorption performance (q=410 mg g -1 ), as well as high antibacterial properties. The oil/water separation can be easily switched by anion exchanging of the PIL segments. Moreover, the multiple functions (oil/water separation, dye absorption, and antibacterial properties) occurred at the same time, and did not interfere with each other. The multifunctional fibrous filter can be easily regenerated by washing with an acid solution, and the absorption capacity is maintained after many recycling tests. These promising features make PIL-grafted PP nonwoven fabric a potential one-step treatment for multicomponent wastewater. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. PREFACE: Dynamic crossover phenomena in water and other glass-forming liquids Dynamic crossover phenomena in water and other glass-forming liquids

    Science.gov (United States)

    Chen, Sow-Hsin; Baglioni, Piero

    2012-02-01

    This special section has been inspired by the workshop on Dynamic Crossover Phenomena in Water and Other Glass-Forming Liquids, held during November 11-13, 2010 at Pensione Bencistà, Fiesole, Italy, a well-preserved 14th century Italian villa tucked high in the hills overlooking Florence. The meeting, an assembly of world renowned scientists, was organized as a special occasion to celebrate the 75th birthday of Professor Sow-Hsin Chen of MIT, a pioneer in several aspects of complex fluids and soft matter physics. The workshop covered a large variety of experimental and theoretical research topics of current interest related to dynamic crossover phenomena in water and, more generally, in other glass-forming liquids. The 30 invited speakers/lecturers and approximately 60 participants were a select group of prominent physicists and chemists from the USA, Europe, Asia and Mexico, who are actively working in the field. Some highlights of this special issue include the following works. Professor Yamaguchi's group and their collaborators present a neutron spin echo study of the coherent intermediate scattering function of heavy water confined in cylindrical pores of MCM-41-C10 silica material in the temperature range 190-298 K. They clearly show that a fragile-to-strong (FTS) dynamic crossover occurs at about 225 K. They attribute the FTS dynamic crossover to the formation of a tetrahedral-like structure, which is preserved in the bulk-like water confined to the central part of the cylindrical pores. Mamontov and Kolesnikov et al study the collective excitations in an aqueous solution of lithium chloride over a temperature range of 205-270 K using neutron and x-ray Rayleigh-Brillouin (coherent) scattering. They detect both the low-frequency and the high-frequency sounds known to exist in pure bulk water above the melting temperature. They also perform neutron (incoherent) and x-ray (coherent) elastic intensity scan measurements. Clear evidence of the crossover in the

  1. Experimental investigations on liquid water removal from the gas diffusion layer by reactant flow in a PEM fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Jiao, Kui; Li, Xianguo [Department of Mechanical and Mechatronics Engineering, University of Waterloo, 200 University Avenue West, Waterloo, Ontario (Canada); Park, Jaewan [Department of Mechanical and Aeronautical Engineering, University of California, Davis One Shields Ave., Davis, CA 95616 (United States)

    2010-09-15

    The cross flow from channel to channel through gas diffusion layer (GDL) under the land could play an important role for water removal in proton exchange membrane (PEM) fuel cells. In this study, characteristics of liquid water removal from GDL have been investigated experimentally, through measuring unsteady pressure drop in a cell which has the GDL initially wet with liquid water. The thickness of GDL is carefully controlled by inserting various thicknesses of metal shims between the plates. It has been found that severe compression of GDL could result in excessive pressure drop from channel inlet to channel outlet. Removing liquid water from GDL by cross flow is difficult for GDL with high compression levels and for low inlet air flow rates. However, effective water removal can still be achieved at high compression levels of GDL if the inlet air flow rate is high. Based on different compressed GDL thicknesses, different GDL porosities and permeabilities were calculated and their effects on the characteristics of liquid water removal from GDL were evaluated. Visualization of liquid water transport has been conducted by using transparent flow channel, and liquid water removal from GDL under the land was observed for all the tested inlet air flow rates, which confirms that cross flow is practically effective to remove the liquid water accumulated in GDL under the land area. (author)

  2. Ultrafast conversions between hydrogen bonded structures in liquid water observed by femtosecond x-ray spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Wen, Haidan; Huse, Nils; Schoenlein, Robert W.; Lindenberg, Aaron M.

    2010-05-01

    We present the first femtosecond soft x-ray spectroscopy in liquids, enabling the observation of changes in hydrogen bond structures in water via core-hole excitation. The oxygen K-edge of vibrationally excited water is probed with femtosecond soft x-ray pulses, exploiting the relation between different water structures and distinct x-ray spectral features. After excitation of the intramolecular OH stretching vibration, characteristic x-ray absorption changes monitor the conversion of strongly hydrogen-bonded water structures to more disordered structures with weaker hydrogen-bonding described by a single subpicosecond time constant. The latter describes the thermalization time of vibrational excitations and defines the characteristic maximum rate with which nonequilibrium populations of more strongly hydrogen-bonded water structures convert to less-bonded ones. On short time scales, the relaxation of vibrational excitations leads to a transient high-pressure state and a transient absorption spectrum different from that of statically heated water.

  3. Quantification of the impact of water as an impurity on standard physico-chemical properties of ionic liquids

    International Nuclear Information System (INIS)

    Andanson, J.-M.; Meng, X.; Traïkia, M.; Husson, P.

    2016-01-01

    Highlights: • Residual water has a negligible impact on density of hydrophobic ionic liquids. • The density of a dry sample can be calculated from the density of a wet ionic liquid. • The viscosity of a dry sample can be calculated from the one of a wet ionic liquid. • Water can be quantified by NMR spectroscopy even in dried hydrophobic ionic liquids. - Abstract: The objective of this work was to quantify the effect of the presence of water as impurity in ionic liquids. First, density and viscosity of five ionic liquids as well as their aqueous solutions were measured. For hydrophobic dried ionic liquids, traces of water (50 ppm) have measurable impact neither on the density nor on the viscosity values. In the concentration range studied (up to 5000 ppm), a linear evolution of the molar volume of the mixture with the mole fraction composition is observed. Practically, this allows to estimate the density of an neat ionic liquid provided (i) the water quantity and (ii) the density of the undried sample are known. This is particularly useful for hydrophilic ionic liquids that are difficult to dry. In the studied concentration range, a linear evolution of the relative viscosity was also depicted as a function of the mass fraction composition. It is thus possible to evaluate the viscosity of the pure ionic liquid knowing the water quantity and the viscosity of the undried sample. The comparison of the results obtained using two viscosimeters confirms that a Stabinger viscosimeter is appropriate to precisely measure ionic liquids viscosities. Second, NMR and IR spectroscopies were used to characterize the pure ionic liquids and their solutions with water. The sensitivity of IR spectroscopy does allow neither the quantification nor the detection of water below 1 mol%. With NMR spectroscopy, water can be quantified using either the intensity or the chemical shift of the water proton peak for mole fractions as low as 200 ppm. It is even possible to detect water in

  4. Purification of inkjet ink from water using liquid phase, electric discharge polymerization and cellulosic membrane filtration.

    Science.gov (United States)

    Jordan, Alexander T; Hsieh, Jeffery S; Lee, Daniel T

    2013-01-01

    A method to separate inkjet ink from water was developed using a liquid phase, electric discharge process. The liquid phase, electric discharge process with filtration or sedimentation was shown to remove 97% of inkjet ink from solutions containing between 0.1-0.8 g/L and was consistent over a range of treatment conditions. Additionally, particle size analysis of treated allyl alcohol and treated propanol confirmed the electric discharge treatment has a polymerization mechanism, and small molecule analysis of treated methanol using gas chromatography and mass spectroscopy confirmed the mechanism was free radical initiated polymerization.

  5. Problems of hydrogen - water vapor - inert gas mixture use in heavy liquid metal coolant technology

    International Nuclear Information System (INIS)

    Ul'yanov, V.V.; Martynov, P.N.; Gulevskij, V.A.; Teplyakov, Yu.A.; Fomin, A.S.

    2014-01-01

    The reasons of slag deposit formation in circulation circuits with heavy liquid metal coolants, which can cause reactor core blockage, are considered. To prevent formation of deposits hydrogen purification of coolant and surfaces of circulation circuit is used. It consists in introduction of gaseous mixtures hydrogen - water vapor - rare gas (argon or helium) directly into coolant flow. The principle scheme of hydrogen purification and the processes occurring during it are under consideration. Measures which make it completely impossible to overlap of the flow cross section of reactor core, steam generators, pumps and other equipment by lead oxides in reactor facilities with heavy liquid metal coolants are listed [ru

  6. Influence of dispersion degree of water drops on efficiency of extinguishing of flammable liquids

    OpenAIRE

    Korolchenko Dmitriy; Voevoda Sergey

    2016-01-01

    Depending on the size of water drops, process of fire extinguishing is focused either in a zone of combustion or on a burning liquid surface. This article considers two alternate solutions of a heat balance equation. The first solution allows us to trace decrease of temperature of a flammable liquid (FL) surface to a temperature lower than fuel flash point at which combustion is stopped. And the second solution allows us to analyze decrease of burnout rate to a negligible value at which steam...

  7. Water liquid-vapor interface subjected to various electric fields: A molecular dynamics study

    Science.gov (United States)

    Nikzad, Mohammadreza; Azimian, Ahmad Reza; Rezaei, Majid; Nikzad, Safoora

    2017-11-01

    Investigation of the effects of E-fields on the liquid-vapor interface is essential for the study of floating water bridge and wetting phenomena. The present study employs the molecular dynamics method to investigate the effects of parallel and perpendicular E-fields on the water liquid-vapor interface. For this purpose, density distribution, number of hydrogen bonds, molecular orientation, and surface tension are examined to gain a better understanding of the interface structure. Results indicate enhancements in parallel E-field decrease the interface width and number of hydrogen bonds, while the opposite holds true in the case of perpendicular E-fields. Moreover, perpendicular fields disturb the water structure at the interface. Given that water molecules tend to be parallel to the interface plane, it is observed that perpendicular E-fields fail to realign water molecules in the field direction while the parallel ones easily do so. It is also shown that surface tension rises with increasing strength of parallel E-fields, while it reduces in the case of perpendicular E-fields. Enhancement of surface tension in the parallel field direction demonstrates how the floating water bridge forms between the beakers. Finally, it is found that application of external E-fields to the liquid-vapor interface does not lead to uniform changes in surface tension and that the liquid-vapor interfacial tension term in Young's equation should be calculated near the triple-line of the droplet. This is attributed to the multi-directional nature of the droplet surface, indicating that no constant value can be assigned to a droplet's surface tension in the presence of large electric fields.

  8. A Liquid Desiccant Cycle for Dehumidification and Fresh Water Supply in Controlled Environment Agriculture

    KAUST Repository

    Lefers, Ryan

    2017-12-01

    Controlled environment agriculture allows the production of fresh food indoors from global locations and contexts where it would not otherwise be possible. Growers in extreme climates and urban areas produce food locally indoors, saving thousands of food import miles and capitalizing upon the demand for fresh, tasty, and nutritious food. However, the growing of food, both indoors and outdoors, consumes huge quantities of water - as much as 70-80% of global fresh water supplies. The utilization of liquid desiccants in a closed indoor agriculture cycle provides the possibility of capturing plant-transpired water vapor. The regeneration/desalination of these liquid desiccants offers the potential to recover fresh water for irrigation and also to re-concentrate the desiccants for continued dehumidification. Through the utilization of solar thermal energy, the process can be completed with a very small to zero grid-energy footprint. The primary research in this dissertation focused on two areas: the dehumidification of indoor environments utilizing liquid desiccants inside membrane contactors and the regeneration of these desiccants using membrane distillation. Triple-bore PVDF hollow fiber membranes yielded dehumidification permeance rates around 0.25-0.31 g m-2 h-1 Pa-1 in lab-scale trials. A vacuum membrane distillation unit utilizing PVDF fibers yielded a flux of 2.8-7.0 kg m-2 hr-1. When the membrane contactor dehumidification system was applied in a bench scale controlled environment agriculture setup, the relative humidity levels responded dynamically to both plant transpiration and dehumidification rates, reaching dynamic equilibrium levels during day and night cycles. In addition, recovered fresh water from distillation was successfully applied for irrigation of crops and concentrated desiccants were successfully reused for dehumidification. If applied in practice, the liquid desiccant system for controlled environment agriculture offers the potential to reduce

  9. Speciation analysis of mercury in water samples by dispersive liquid-liquid microextraction coupled to capillary electrophoresis.

    Science.gov (United States)

    Yang, Fangfang; Li, Jinhua; Lu, Wenhui; Wen, Yingying; Cai, Xiaoqiang; You, Jinmao; Ma, Jiping; Ding, Yangjun; Chen, Lingxin

    2014-02-01

    In this study, a method of pretreatment and speciation analysis of mercury by dispersive liquid-liquid microextraction along with CE was developed. The method was based on the fact that mercury species including methylmercury (MeHg), ethylmercury (EtHg), phenylmercury (PhHg), and Hg(II) were complexed with 1-(2-pyridylazo)-2-naphthol to form hydrophobic chelates and l-cysteine could displace 1-(2-pyridylazo)-2-naphthol to form hydrophilic chelates with the four mercury species. Factors affecting complex formation and extraction efficiency, such as pH value, type, and volume of extractive solvent and disperser solvent, concentration of the chelating agent, ultrasonic time, and buffer solution were investigated. Under the optimal conditions, the enrichment factors were 102, 118, 547, and 46, and the LODs were 1.79, 1.62, 0.23, and 1.50 μg/L for MeHg, EtHg, PhHg, and Hg(II), respectively. Method precisions (RSD, n = 5) were in the range of 0.29-0.54% for migration time, and 3.08-7.80% for peak area. Satisfactory recoveries ranging from 82.38 to 98.76% were obtained with seawater, lake, and tap water samples spiked at three concentration levels, respectively, with RSD (n = 5) of 1.98-7.18%. This method was demonstrated to be simple, convenient, rapid, cost-effective, and environmentally benign, and could be used as an ideal alternative to existing methods for analyzing trace residues of mercury species in water samples. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Application of an immobilized ionic liquid for the passive sampling of perfluorinated substances in water.

    Science.gov (United States)

    Wang, Lei; Gong, Xinying; Wang, Ruonan; Gan, Zhiwei; Lu, Yuan; Sun, Hongwen

    2017-09-15

    Ionic liquids have been used to efficiently extract a wide range of polar and nonpolar organic contaminants from water. In this study, imidazole ionic liquids immobilized on silica gel were synthesized through a chemical bonding method, and the immobilized dodecylimidazolium ionic liquid was selected as the receiving phase material in a POCIS (polar organic chemical integrative sampler) like passive sampler to monitor five perfluoroalkyl substances (PFASs) in water. Twenty-one days of integrative accumulation was conducted in laboratory scale experiments, and the accumulated PFASs in the samplers were eluted and analyzed by high performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). The partitioning coefficients of most PFASs between sampler sorbents and water in the immobilized ionic liquid (IIL)-sampler were higher than those in the HLB-sampler, especially for compounds with shorter alkyl chains. The effects of flow velocity, temperature, dissolved organic matter (DOM) and pH on the uptake of these analytes were also evaluated. Under the experimental conditions, the uptake of PFASs in the IIL-sampler slightly increased with the flow velocity and temperature, while different influences of DOM and pH on the uptake of PFAS homologues with short or long chains were observed. The designed IIL-samplers were applied in the influent and effluent of a wastewater treatment plant. All five PFASs could be accumulated in the samplers, with concentrations ranging from 6.5×10 -3 -3.6×10 -1 nmol/L in the influent and from 1.3×10 -2 -2.2×10 -1 nmol/L in the effluent. The calculated time-weighted average concentrations of most PFASs fit well with the detected concentrations of the active sampling, indicating the applicability of the IIL-sampler in monitoring these compounds in water. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Initiation of secondary ice production in clouds

    Directory of Open Access Journals (Sweden)

    S. C. Sullivan

    2018-02-01

    Full Text Available Disparities between the measured concentrations of ice-nucleating particles (INPs and in-cloud ice crystal number concentrations (ICNCs have led to the hypothesis that mechanisms other than primary nucleation form ice in the atmosphere. Here, we model three of these secondary production mechanisms – rime splintering, frozen droplet shattering, and ice–ice collisional breakup – with a six-hydrometeor-class parcel model. We perform three sets of simulations to understand temporal evolution of ice hydrometeor number (Nice, thermodynamic limitations, and the impact of parametric uncertainty when secondary production is active. Output is assessed in terms of the number of primarily nucleated ice crystals that must exist before secondary production initiates (NINP(lim as well as the ICNC enhancement from secondary production and the timing of a 100-fold enhancement. Nice evolution can be understood in terms of collision-based nonlinearity and the phasedness of the process, i.e., whether it involves ice hydrometeors, liquid ones, or both. Ice–ice collisional breakup is the only process for which a meaningful NINP(lim exists (0.002 up to 0.15 L−1. For droplet shattering and rime splintering, a warm enough cloud base temperature and modest updraft are the more important criteria for initiation. The low values of NINP(lim here suggest that, under appropriate thermodynamic conditions for secondary ice production, perturbations in cloud concentration nuclei concentrations are more influential in mixed-phase partitioning than those in INP concentrations.

  12. (Liquid + liquid) equilibrium of {l_brace}water + phenol + (1-butanol, or 2-butanol, or tert-butanol){r_brace} systems

    Energy Technology Data Exchange (ETDEWEB)

    Hadlich de Oliveira, Leonardo [School of Chemical Engineering, State University of Campinas, UNICAMP, P.O. Box 6066, 13083-970 Campinas-SP (Brazil); Aznar, Martin, E-mail: maznar@feq.unicamp.b [School of Chemical Engineering, State University of Campinas, UNICAMP, P.O. Box 6066, 13083-970 Campinas-SP (Brazil)

    2010-11-15

    (Liquid + liquid) equilibrium (LLE) and binodal curve data were determined for the systems (water + phenol + tert-butanol) at T = 298.15 K, (water + phenol + 2-butanol) and (water + phenol + 1-butanol) at T = 298.15 K and T = 313.15 K by the combined techniques of densimetry and refractometry. Type I curve (for tert-butanol) and Type II curves (for 1- and 2-butanol) were found. The data were correlated with the NRTL model and the parameters estimated present root mean square deviations below 2% for the system with tert-butanol and lower than 0.8% for the other systems.

  13. Thermal conductivity coefficients of water and heavy water in the liquid state up to 3700C

    International Nuclear Information System (INIS)

    Le Neindre, B.; Bury, P.; Tufeu, R.; Vodar, B.

    1976-01-01

    The thermal conductivity coefficients of water and heavy water of 99.75 percent isotopic purity were measured using a coaxial cylinder apparatus, covering room temperature to their critical temperatures, and pressures from 1 to 500 bar for water, and from 1 to 1000 bar for heavy water. Following the behavior of the thermal conductivity coefficient of water, which shows a maximum close to 135 0 C, the thermal conductivity coefficient of heavy water exhibits a maximum near 95 0 C and near saturation pressures. This maximum is displaced to higher temperatures when the pressure is increased. Under the same temperature and pressure conditions the thermal conductivity coefficient of heavy water was lower than for water. The pressure effect was similar for water and heavy water. In the temperature range of our experiments, isotherms of thermal conductivity coefficients were almost linear functions of density

  14. Formation of radical and active chemical species in electrical discharge plasma in the presence of liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Locke, B.R.; Shih, K.Y.; Burlica, R. [Florida State Univ., Tallahassee, FL (United States). Dept. of Chemical and Biomedical Engineering

    2010-07-01

    This study investigated the interactions of plasma with liquid water using a combination of emission spectroscopy of radical and atomic species and direct measurements of more stable chemical compounds. The study focused on electrical discharge plasma formed directly in liquid water and on discharges formed in the gas phase above liquid water, in bubbles in liquid water, and in the gas phase with water droplet spray that result in a variety of active chemical species that can be used for pollution control as well as other applications in biomedical and materials engineering. The purpose was to improve the design and operation of plasma reactors for a variety of applications. This presentation also reviewed the mechanisms for the formation of active chemical species such as hydroxyl and other radicals, hydrogen peroxide and molecular hydrogen, in electrical discharge plasma formed in the presence of water.

  15. Water hammer phenomena occurring in nuclear power installations while filling horizontal pipe containing saturated steam with liquid

    International Nuclear Information System (INIS)

    Selivanov, Y.F.; Kirillov, P.L.; Yefanov, A.D.

    1995-01-01

    The potentiality of the water hammer occurrence in nuclear reactor loop components has been considered under the conditions of filling a steam-containing pipeline leg involving horizontal and vertical sections with liquid subcooled to the saturation temperature. As a result of free discharging from the tank, the liquid enters the horizontal pipeline. When the liquid slug formation in the pipeline is fulfilled. The pressure drop being occurred in steam flowing along the pipelines causes the liquid slug to move to the pipeline inlet. When the liquid slug decelerates, a water hammer occurs. This mechanism of water hammer occurrence is tested by experiments. The regimes of the occurrence of multiple considerable water hammers were identified

  16. Water hammer phenomena occurring in nuclear power installations while filling horizontal pipe containing saturated steam with liquid

    Energy Technology Data Exchange (ETDEWEB)

    Selivanov, Y.F.; Kirillov, P.L.; Yefanov, A.D. [Institute of Physics and Power Engineering, Obninsk (Russian Federation)

    1995-09-01

    The potentiality of the water hammer occurrence in nuclear reactor loop components has been considered under the conditions of filling a steam-containing pipeline leg involving horizontal and vertical sections with liquid subcooled to the saturation temperature. As a result of free discharging from the tank, the liquid enters the horizontal pipeline. When the liquid slug formation in the pipeline is fulfilled. The pressure drop being occurred in steam flowing along the pipelines causes the liquid slug to move to the pipeline inlet. When the liquid slug decelerates, a water hammer occurs. This mechanism of water hammer occurrence is tested by experiments. The regimes of the occurrence of multiple considerable water hammers were identified.

  17. Comparison of dispersive liquid-liquid microextraction and hollow fiber liquid-liquid-liquid microextraction for the determination of fentanyl, alfentanil, and sufentanil in water and biological fluids by high-performance liquid chromatography.

    Science.gov (United States)

    Saraji, Mohammad; Khalili Boroujeni, Malihe; Hajialiakbari Bidgoli, Ali Akbar

    2011-06-01

    Dispersive liquid-liquid microextraction (DLLME) and hollow fiber liquid-liquid-liquid microextraction (HF-LLLME) combined with HPLC-DAD have been applied for the determination of three narcotic drugs (alfentanil, fentanyl, and sufentanil) in biological samples (human plasma and urine). Different DLLME parameters influencing the extraction efficiency such as type and volume of the extraction solvent and the disperser solvent, concentration of NaOH, and salt addition were investigated. In the HF-LLLME, the effects of important parameters including organic solvent type, concentration of NaOH as donor solution, concentration of H(2)SO(4) as acceptor phase, salt addition, stirring rate, temperature, and extraction time were investigated and optimized. The results showed that both extraction methods exhibited good linearity, precision, enrichment factor, and detection limit. Under optimal condition, the limits of detection ranged from 0.4 to 1.9 μg/L and from 1.1 to 2.3 μg/L for DLLME and HF-LLLME, respectively. For DLLME, the intra- and inter-day precisions were 1.7-6.4% and 14.2-15.9%, respectively; and for HF-LLLME were 0.7-5.2% and 3.3-10.1%, respectively. The enrichment factors were from 275 to 325 and 190 to 237 for DLLME and HF-LLLME, respectively. The applicability of the proposed methods was investigated by analyzing biological samples. For analysis of human plasma and urine samples, HF-LLLME showed higher precision, more effective sample clean-up, higher extraction efficiency, lower organic solvent consumption than DLLME.

  18. First Principles Modeling of Structure and Transport in Solid Polymer Electrolytes, Ionic Liquids, and Methanol/Water Mixtures

    Science.gov (United States)

    2016-02-10

    the general formula: PEO6:XPF6, where X = H, Li, or Na; (2) methanol /water solution over a range of methanol mole fractions (0 to 1); and (3...Electrolytes, Ionic Liquids, and Methanol /Water Mixtures The views, opinions and/or findings contained in this report are those of the author(s) and...dynamics, quantum chemistry, electronic structure, solid polymer electrolytes, ionic liquids, methanol /water mixtures REPORT DOCUMENTATION PAGE 11

  19. Determination of selected azaarenes in water by bonded-phase extraction and liquid chromatography

    Science.gov (United States)

    Steinheimer, T.R.; Ondrus, M.G.

    1986-01-01

    A method for the rapid and simple quantitative determination of quinoline, isoquinoline, and five selected three-ring azaarenes in water has been developed. The azaarene fraction is separated from its carbon analogues on n-octadecyl packing material by edition with acidified water/acetonitrile. Concentration as great as 1000-fold is achieved readily. Instrumental analysis involves high-speed liquid chromatography on flexible-walled, wide-bore columns with fluorescence and ultraviolet detection at several wavelengths employing filter photometers in series. Method-validation data is provided as azaarene recovery efficiency from fortified samples. Distilled water, river water, contaminated ground water, and secondary-treatment effluent have been tested. Recoveries at part-per-billion levels are nearly quantitative for the three-ring compounds, but they decrease for quinoline and isoquinoline. ?? 1986 American Chemical Society.

  20. (Liquid + liquid) equilibria of (water + linalool + limonene) ternary system at T = (298.15, 308.15, and 318.15) K

    Energy Technology Data Exchange (ETDEWEB)

    Gramajo de Doz, Monica B. [Departamento de Fisica, Facultad de Ciencias Exactas y Tecnologia, Universidad Nacional de Tucuman, Avenida Independencia 1800, 4000 Tucuman (Argentina)], E-mail: mgramajo@herrera.unt.edu.ar; Cases, Alicia M.; Solimo, Horacio N. [Departamento de Fisica, Facultad de Ciencias Exactas y Tecnologia, Universidad Nacional de Tucuman, Avenida Independencia 1800, 4000 Tucuman (Argentina)

    2008-11-15

    (Liquid + liquid) equilibrium (LLE) data for {l_brace}water (1) + linalool (2) + limonene (3){r_brace} ternary system at T = (298.15, 308.15, and 318.15 {+-} 0.05) K are reported. The organic chemicals were quantified by gas chromatography using a flame ionisation detector while water was quantified using a thermal conductivity detector. The effect of the temperature on (liquid + liquid) equilibrium is determined and discussed. Experimental data for the ternary mixture are compared with values calculated by the NRTL and UNIQUAC equations, and predicted by means of the UNIFAC group contribution method. It is found that the UNIQUAC and NRTL models provide a good correlation of the solubility curve at these three temperatures, while comparing the calculated values with the experimental ones, the best fit is obtained with the NRTL model. Finally, the UNIFAC model provides poor results, since it predicts a greater heterogeneous region than experimentally observed.

  1. (Liquid + liquid) equilibria of (water + linalool + limonene) ternary system at T = (298.15, 308.15, and 318.15) K

    International Nuclear Information System (INIS)

    Gramajo de Doz, Monica B.; Cases, Alicia M.; Solimo, Horacio N.

    2008-01-01

    (Liquid + liquid) equilibrium (LLE) data for {water (1) + linalool (2) + limonene (3)} ternary system at T = (298.15, 308.15, and 318.15 ± 0.05) K are reported. The organic chemicals were quantified by gas chromatography using a flame ionisation detector while water was quantified using a thermal conductivity detector. The effect of the temperature on (liquid + liquid) equilibrium is determined and discussed. Experimental data for the ternary mixture are compared with values calculated by the NRTL and UNIQUAC equations, and predicted by means of the UNIFAC group contribution method. It is found that the UNIQUAC and NRTL models provide a good correlation of the solubility curve at these three temperatures, while comparing the calculated values with the experimental ones, the best fit is obtained with the NRTL model. Finally, the UNIFAC model provides poor results, since it predicts a greater heterogeneous region than experimentally observed

  2. Multisensor Advanced Climatology Mean Liquid Water Path Diurnal Cycle L3 Monthly 1 degree x 1 degree V1 (MACLWP_diurnal) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — The Multi-Sensor Advanced Climatology of Liquid Water Path (MAC-LWP) data set contains monthly 1.0-degree ocean-only estimates of cloud liquid water path...

  3. Multisensor Advanced Climatology Mean Liquid Water Path L3 Monthly 1 degree X 1 degree V1 (MACLWP_mean) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — The Multi-Sensor Advanced Climatology of Liquid Water Path (MAC-LWP) data set contains monthly 1.0-degree ocean-only estimates of cloud liquid water path...

  4. Multisensor Advanced Climatology Total Liquid Water Path L3 Monthly 1 degree x 1 degree V1 (MACTWP_mean) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — The Multi-Sensor Advanced Climatology of Liquid Water Path (MAC-LWP) data set contains monthly 1.0-degree ocean-only estimates of cloud liquid water path...

  5. Liquid-solid contact measurements using a surface thermocouple temperature probe in atmospheric pool boiling water

    International Nuclear Information System (INIS)

    Lee, L.Y.W.; Chen, J.C.; Nelson, R.A.

    1984-01-01

    Objective was to apply the technique of using a microthermocouple flush-mounted at the boiling surface for the measurement of the local-surface-temperature history in film and transition boiling on high temperature surfaces. From this measurement direct liquid-solid contact in film and transition boiling regimes was observed. In pool boiling of saturated, distilled, deionized water on an aluminum-coated copper surface, the time-averaged, local-liquid-contact fraction increased with decreasing surface superheat. Average contact duration increased monotonically with decreasing surface superheat, while frequency of liquid contact reached a maximum of approx. 50 contacts/s at a surface superheat of approx. 100 K and decreased gradually to 30 contacts/s near the critical heat flux. The liquid-solid contact duration distribution was dominated by short contacts 4 ms at low surface superheats, passing through a relatively flat contact duration distribution at about 80 0 K. Results of this paper indicate that liquid-solid contacts may be the dominant mechanism for energy transfer in the transition boiling process

  6. Generation of reactive species in atmospheric pressure dielectric barrier discharge with liquid water

    Science.gov (United States)

    Zelong, ZHANG; Jie, SHEN; Cheng, CHENG; Zimu, XU; Weidong, XIA

    2018-04-01

    Atmospheric pressure helium/water dielectric barrier discharge (DBD) plasma is used to investigate the generation of reactive species in a gas-liquid interface and in a liquid. The emission intensity of the reactive species is measured by optical emission spectroscopy (OES) with different discharge powers at the gas-liquid interface. Spectrophotometry is used to analyze the reactive species induced by the plasma in the liquid. The concentration of OH radicals reaches 2.2 μm after 3 min of discharge treatment. In addition, the concentration of primary long-lived reactive species such as H2O2, {{{{NO}}}3}- and O3 are measured based on plasma treatment time. After 5 min of discharge treatment, the concentration of H2O2, {{{{NO}}}3}-, and O3 increased from 0 mg · L-1 to 96 mg · L-1, 19.5 mg · L-1, and 3.5 mg · L-1, respectively. The water treated by plasma still contained a considerable concentration of reactive species after 6 h of storage. The results will contribute to optimizing the DBD plasma system for biological decontamination.

  7. Decomposition behavior of hemicellulose and lignin in the step-change flow rate liquid hot water.

    Science.gov (United States)

    Zhuang, Xinshu; Yu, Qiang; Wang, Wen; Qi, Wei; Wang, Qiong; Tan, Xuesong; Yuan, Zhenhong

    2012-09-01

    Hemicellulose and lignin are the main factors limiting accessibility of hydrolytic enzymes besides the crystallinity of cellulose. The decomposition behavior of hemicellulose and lignin in the step-change flow rate hot water system was investigated. Xylan removal increased from 64.53% for batch system (solid concentration 4.25% w/v, 18 min, 184°C) to 83.78% at high flow rates of 30 ml/min for 8 min, and then 10 ml/min for 10 min. Most of them (80-90%) were recovered as oligosaccharide. It was hypothesized that the flowing water could enhance the mass transfer to improve the sugars recovery. In addition, the solubilization mechanism of lignin in the liquid hot water was proposed according to the results of Fourier transform-infrared spectroscopy and scanning electron microscopy of the water-insoluble fraction and gas chromatography-mass spectrometry of the water-soluble fraction. It was proposed that lignin in the liquid hot water first migrated out of the cell wall in the form of molten bodies, and then flushed out of the reactor. A small quantity of them was further degraded into monomeric products such as vanillin, syringe aldehyde, coniferyl aldehyde, ferulic acid, and p-hydroxy-cinnamic acid. All of these observations would provide important information for the downstream processing, such as purification and concentration of sugars and the enzymatic digestion of residual solid.

  8. Liquid-liquid equilibria of propionic acid - water - solvent (n-hexane, cyclohexane, cyclohexanol and cyclohexyl acetate ternaries at 298.15 K

    Directory of Open Access Journals (Sweden)

    Özmen D.

    2004-01-01

    Full Text Available The experimental liquid-liquid equilibrium data on propionic acid-water-solvent ternary mixtures at a temperature of 298.15 K are presented. The solvents are n-hexane, cyclohexane, cyclohexanol and cyclohexyl acetate. The distribution coefficients and separation factors are reported. The tie line data are correlated using the methods of Othmer-Tobias and Hand. The experimental results are compared with the values predicted by the UNIFAC group-contribution method.

  9. Operational procedures for reduction of liquid wastes from pressurized water reactors

    International Nuclear Information System (INIS)

    Ribeiro, Gilberto Soares; Lopes, Roberto Machado

    1996-01-01

    This work is based upon the fact that, during core life, it is necessary to make up for the Reactor Coolant System (RCS) losses and also to dilute the same system to compensate for the fuel depletion and core fission products poisoning. It was developed taking into consideration the possibility of doing both operations without having an additive effect in terms of liquid waste production. In other words it is always desirable to compensate for the RCS losses with pure water (boron free) instead of doing it with borated water, because some time later it will be necessary to dilute the RCS. By doing this, at Angra Unit I, it is possible to reduce about 20.5% in the liquid waste production what could correspond to volumes ranging from 250,000 to 300,000 liters, per fuel cycle. Besides that, there will be a great reduction of the total activity released to the environment. (author)

  10. Communications: On artificial frequency shifts in infrared spectra obtained from centroid molecular dynamics: Quantum liquid water

    Science.gov (United States)

    Ivanov, Sergei D.; Witt, Alexander; Shiga, Motoyuki; Marx, Dominik

    2010-01-01

    Centroid molecular dynamics (CMD) is a popular method to extract approximate quantum dynamics from path integral simulations. Very recently we have shown that CMD gas phase infrared spectra exhibit significant artificial redshifts of stretching peaks, due to the so-called "curvature problem" imprinted by the effective centroid potential. Here we provide evidence that for condensed phases, and in particular for liquid water, CMD produces pronounced artificial redshifts for high-frequency vibrations such as the OH stretching band. This peculiar behavior intrinsic to the CMD method explains part of the unexpectedly large quantum redshifts of the stretching band of liquid water compared to classical frequencies, which is improved after applying a simple and rough "harmonic curvature correction."

  11. Influence of dispersion degree of water drops on efficiency of extinguishing of flammable liquids

    Directory of Open Access Journals (Sweden)

    Korolchenko Dmitriy

    2016-01-01

    Full Text Available Depending on the size of water drops, process of fire extinguishing is focused either in a zone of combustion or on a burning liquid surface. This article considers two alternate solutions of a heat balance equation. The first solution allows us to trace decrease of temperature of a flammable liquid (FL surface to a temperature lower than fuel flash point at which combustion is stopped. And the second solution allows us to analyze decrease of burnout rate to a negligible value at which steam-air mixture becomes nonflammable. As a result of solve of a heat balance equation it was made the following conclusion: water drops which size is equal to 100 μm will completely evaporate in a zone of combustion with extent of 1 m if the flying speed of drops is even 16 mps (acc. to Stokes v = 3 mps; whereas drops of larger size will evaporate only partially.

  12. Nuclear spin optical rotation and Faraday effect in gaseous and liquid water.

    Science.gov (United States)

    Pennanen, Teemu S; Ikäläinen, Suvi; Lantto, Perttu; Vaara, Juha

    2012-05-14

    Nuclear spin optical rotation (NSOR) of linearly polarized light, due to the nuclear spins through the Faraday effect, provides a novel probe of molecular structure and could pave the way to optical detection of nuclear magnetization. We determine computationally the effects of the liquid medium on NSOR and the Verdet constant of Faraday rotation (arising from an external magnetic field) in water, using the recently developed theory applied on a first-principles molecular dynamics trajectory. The gas-to-liquid shifts of the relevant antisymmetric polarizability and, hence, NSOR magnitude are found to be -14% and -29% for (1)H and (17)O nuclei, respectively. On the other hand, medium effects both enhance the local electric field in water and, via bulk magnetization, the local magnetic field. Together these two effects partially cancel the solvation influence on the single-molecular property. We find a good agreement for the hydrogen NSOR with a recent pioneering experiment on H(2)O(l).

  13. Trust management in cloud services

    CERN Document Server

    Noor, Talal H; Bouguettaya, Athman

    2014-01-01

    This book describes the design and implementation of Cloud Armor, a novel approach for credibility-based trust management and automatic discovery of cloud services in distributed and highly dynamic environments. This book also helps cloud users to understand the difficulties of establishing trust in cloud computing and the best criteria for selecting a service cloud. The techniques have been validated by a prototype system implementation and experimental studies using a collection of real world trust feedbacks on cloud services.The authors present the design and implementation of a novel pro

  14. Standard Test Method for Preparing Aircraft Cleaning Compounds, Liquid Type, Water Base, for Storage Stability Testing

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2002-01-01

    1.1 This test method covers the determination of the stability in storage, of liquid, water-base chemical cleaning compounds, used to clean the exterior surfaces of aircraft. 1.2 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 establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  15. Low-energy electron inelastic mean free paths for liquid water.

    Science.gov (United States)

    Nguyen-Truong, Hieu T

    2018-04-18

    We improve the Mermin-Penn algorithm (MPA) for determining the energy loss function (ELF) within the dielectric formalism. The present algorithm is applicable not only to real metals, but also to materials that have an energy gap in the excitation spectrum. Applying the improved MPA to liquid water, we show that the present algorithm is able to address the ELF overestimation at the energy gap, and the calculated results are in good agreement with experimental data.

  16. Low-energy electron inelastic mean free paths for liquid water

    Science.gov (United States)

    Nguyen-Truong, Hieu T.

    2018-04-01

    We improve the Mermin–Penn algorithm (MPA) for determining the energy loss function (ELF) within the dielectric formalism. The present algorithm is applicable not only to real metals, but also to materials that have an energy gap in the excitation spectrum. Applying the improved MPA to liquid water, we show that the present algorithm is able to address the ELF overestimation at the energy gap, and the calculated results are in good agreement with experimental data.

  17. Expanding the calculation of activation volumes: Self-diffusion in liquid water.

    Science.gov (United States)

    Piskulich, Zeke A; Mesele, Oluwaseun O; Thompson, Ward H

    2018-04-07

    A general method for calculating the dependence of dynamical time scales on macroscopic thermodynamic variables from a single set of simulations is presented. The approach is applied to the pressure dependence of the self-diffusion coefficient of liquid water as a particularly useful illustration. It is shown how the activation volume associated with diffusion can be obtained directly from simulations at a single pressure, avoiding approximations that are typically invoked.

  18. Expanding the calculation of activation volumes: Self-diffusion in liquid water

    Science.gov (United States)

    Piskulich, Zeke A.; Mesele, Oluwaseun O.; Thompson, Ward H.

    2018-04-01

    A general method for calculating the dependence of dynamical time scales on macroscopic thermodynamic variables from a single set of simulations is presented. The approach is applied to the pressure dependence of the self-diffusion coefficient of liquid water as a particularly useful illustration. It is shown how the activation volume associated with diffusion can be obtained directly from simulations at a single pressure, avoiding approximations that are typically invoked.

  19. Calculated depth-dose distributions for H+ and He+ beams in liquid water

    International Nuclear Information System (INIS)

    Garcia-Molina, Rafael; Abril, Isabel; Denton, Cristian D.; Heredia-Avalos, Santiago; Kyriakou, Ioanna; Emfietzoglou, Dimitris

    2009-01-01

    We have calculated the dose distribution delivered by proton and helium beams in liquid water as a function of the target-depth, for incident energies in the range 0.5-10 MeV/u. The motion of the projectiles through the stopping medium is simulated by a code that combines Monte Carlo and a finite differences algorithm to consider the electronic stopping power, evaluated in the dielectric framework, and the multiple nuclear scattering with the target nuclei. Changes in projectile charge-state are taken into account dynamically as it moves through the target. We use the MELF-GOS model to describe the energy loss function of liquid water, obtaining a value of 79.4 eV for its mean excitation energy. Our calculated stopping powers and depth-dose distributions are compared with those obtained using other methods to describe the energy loss function of liquid water, such as the extended Drude and the Penn models, as well as with the prediction of the SRIM code and the tables of ICRU.

  20. A surprisingly simple correlation between the classical and quantum structural networks in liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Hamm, Peter; Fanourgakis, George S.; Xantheas, Sotiris S.

    2017-08-14

    Nuclear quantum effects in liquid water have profound implications for several of its macroscopic properties related to structure, dynamics, spectroscopy and transport. Although several of water’s macroscopic properties can be reproduced by classical descriptions of the nuclei using potentials effectively parameterized for a narrow range of its phase diagram, a proper account of the nuclear quantum effects is required in order to ensure that the underlying molecular interactions are transferable across a wide temperature range covering different regions of that diagram. When performing an analysis of the hydrogen bonded structural networks in liquid water resulting from the classical (class.) and quantum (q.m.) descriptions of the nuclei with the transferable, flexible, polarizable TTM3-F interaction potential, we found that the two results can be superimposed over the temperature range of T=270-350 K using a surprisingly simple, linear scaling of the two temperatures according to T(q.m.)=aT(class)- T , where a=1.2 and T=51 K. The linear scaling and constant shift of the temperature scale can be considered as a generalization of the previously reported temperature shifts (corresponding to structural changes and the melting T) induced by quantum effects in liquid water.

  1. Lysozyme Solubility and Conformation in Neat Ionic Liquids and Their Mixtures with Water.

    Science.gov (United States)

    Strassburg, Stephen; Bermudez, Harry; Hoagland, David

    2016-06-13

    The room temperature solubility of a number of model proteins is assessed for a diverse set of neat ionic liquids (ILs). For two soluble protein-IL pairs, lysozyme in [C2MIM][EtSO4] (1-ethyl-3-methylimidazolium ethylsulfate) and in [C2,4,4,4P][Et2PO4] (tributyl(ethyl)phosphonium diethylphosphate), protein solubility and structure at various temperatures are probed by dynamic light scattering (assessing dissolved molecular size), turbidimetry (reflecting degree of solubility), and Fourier transform infrared spectroscopy (uncovering helical secondary structure). As compared to aqueous environments, [C2,4,4,4P][Et2PO4] thermally stabilizes protein size and secondary structure while [C2MIM][EtSO4] does the opposite. Lysozyme denatured in [C2MIM][EtSO4] does not aggregate, presumably due to an absence of hydrophobic interactions, and the denaturation appears thermally reversible. Both ILs at room temperature are miscible with water in all proportions, but to create the corresponding ternary mixtures with protein, the order of mixing is important. Mixed to avoid additions of water to IL-dissolved protein, stable solutions are obtained with [C2MIM][EtSO4] at all solvent compositions. When water is added to IL-rich solutions, liquid-liquid demixing is noted.

  2. Isobaric-isothermal Monte Carlo simulations from first principles: Application to liquid water at ambient conditions

    Energy Technology Data Exchange (ETDEWEB)

    McGrath, M; Siepmann, J I; Kuo, I W; Mundy, C J; VandeVondele, J; Hutter, J; Mohamed, F; Krack, M

    2004-12-02

    A series of first principles Monte Carlo simulations in the isobaric-isothermal ensemble were carried out for liquid water at ambient conditions (T = 298 K and p = 1 atm). The Becke-Lee-Yang-Parr (BLYP) exchange and correlation energy functionals and norm-conserving Goedecker-Teter-Hutter (GTH) pseudopotentials were employed with the CP2K simulation package to examine systems consisting of 64 water molecules. The fluctuations in the system volume encountered in simulations in the isobaric-isothermal ensemble requires a reconsideration of the suitability of the typical charge density cutoff and the regular grid generation method previously used for the computation of the electrostatic energy in first principles simulations in the microcanonical or canonical ensembles. In particular, it is noted that a much higher cutoff is needed and that the most computationally efficient method of creating grids can result in poor simulations. Analysis of the simulation trajectories using a very large charge density cutoff at 1200 Ry and four different grid generation methods point to a substantially underestimated liquid density of about 0.85 g/cm{sup 3} resulting in a somewhat understructured liquid (with a value of about 2.7 for the height of the first peak in the oxygen/oxygen radial distribution function) for BLYP-GTH water at ambient conditions.

  3. Determination of 226Ra and 224Ra in drinking waters by liquid scintillation counting

    International Nuclear Information System (INIS)

    Manjon, G.; Vioque, I.; Moreno, H.; Garcia-Tenorio, R.; Garcia-Leon, M.

    1997-01-01

    A method for the determination of Ra-isotopes in water samples has been developed. Ra is coprecipitated with Ba as sulphate. The precipitate is then dissolved with EDTA and counted with a liquid scintillation system after mixing with a scintillation cocktail. The study of the temporal evolution of the separated activity gives the isotopic composition of the sample, i.e. the 224 Ra and 226 Ra contribution to the total activity. The method has been applied to some Spanish drinking waters. (author)

  4. Electronic structure effects in liquid water studied by photoelectron spectroscopy and density functional theory

    Energy Technology Data Exchange (ETDEWEB)

    Nordlund, Dennis; Odelius, Michael; Bluhm, Hendrik; Ogasawara, Hirohito; Pettersson, Lars G.M.; Nilsson, Anders

    2008-04-29

    We present valence photoelectron emission spectra of liquid water in comparison with gas-phase water, ice close to the melting point, low temperature amorphous and crystalline ice. All aggregation states have major electronic structure changes relative to the free molecule, with rehybridization and development of bonding and anti-bonding states accompanying the hydrogen bond formation. Sensitivity to the local structural order, most prominent in the shape and splitting of the occupied 3a{sub 1} orbital, is understood from the electronic structure averaging over various geometrical structures, and reflects the local nature of the orbital interaction.

  5. Impact of water dilution and cation tail length on ionic liquid characteristics: Interplay between polar and non-polar interactions

    Science.gov (United States)

    Hegde, Govind A.; Bharadwaj, Vivek S.; Kinsinger, Corey L.; Schutt, Timothy C.; Pisierra, Nichole R.; Maupin, C. Mark

    2016-08-01

    The recalcitrance of lignocellulosic biomass poses a major challenge that hinders the economical utilization of biomass for the production of biofuel, plastics, and chemicals. Ionic liquids have become a promising solvent that addresses many issues in both the pretreatment process and the hydrolysis of the glycosidic bond for the deconstruction of cellulosic materials. However, to make the use of ionic liquids economically viable, either the cost of ionic liquids must be reduced, or a less expensive solvent (e.g., water) may be added to reduce the overall amount of ionic liquid used in addition to reducing the viscosity of the binary liquid mixture. In this work, we employ atomistic molecular dynamics simulations to investigate the impact of water dilution on the overall liquid structure and properties of three imidazolium based ionic liquids. It is found that ionic liquid-water mixtures exhibit characteristics that can be grouped into two distinct regions, which are a function of the ionic liquid concentration. The trends observed in each region are found to correlate with the ordering in the local structure of the ionic liquid that arises from the dynamic interactions between the ion pairs. Simulation results suggest that there is a high level of local ordering in the molecular structure at high concentrations of ionic liquids that is driven by the aggregation of the cationic tails and the anion-water interactions. It is found that as the concentration of ionic liquids in the binary mixture is decreased, there is a point at which the competing self and cross interaction energies between the ionic liquid and water shifts away from a cation-anion dominated regime, which results in a significant change in the mixture properties. This break point, which occurs around 75% w/w ionic liquids, corresponds to the point at which water molecules percolate into the ionic liquid network disrupting the ionic liquids' nanostructure. It is observed that as the cationic alkyl

  6. Photochemical synthesis of silver particles in Tween 20/water/ionic liquid microemulsions.

    Science.gov (United States)

    Harada, Masafumi; Kimura, Yoshifumi; Saijo, Kenji; Ogawa, Tetsuya; Isoda, Seiji

    2009-11-15

    Metal particles of silver (Ag) were synthesized by the photoreduction of silver perchlorate (AgClO(4)) in water-in-ionic liquid (ILs) microemulsions consisting of Tween 20, water and ionic liquids. The ILs were tetrafluoroborate anions associated with the cations 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIm][BF(4)]) and 1-octyl-3-methylimidazolium tetrafluoroborate ([OMIm][BF(4)]). The time evolution of Ag particle formation by photoreduction using UV-irradiation was investigated by UV-Vis, cryo-TEM, extended X-ray absorption fine structure (EXAFS) and small angle X-ray scattering (SAXS) measurements. The average diameter of the metallic Ag particles prepared in the water-in-[BMIm][BF(4)] and water-in-[OMIm][BF(4)] microemulsions was estimated from TEM to be 8.9 and 4.9nm, respectively, which was consistent with that obtained from the SAXS analysis. Using Guinier plots in a low q-range (ionic precursors of AgClO(4) before reduction and Ag particles after reduction, in the microemulsions, was estimated to be about 20-40nm. The diameter of the water droplets increased as a function of photoreduction time because of the formation of Ag particles and their aggregates. EXAFS analysis indicated that Ag(+) ions were completely reduced to Ag(0) atoms during the photoreduction, followed by the formation of larger Ag particles.

  7. Reduced Near-Resonant Vibrational Coupling at the Surfaces of Liquid Water and Ice.

    Science.gov (United States)

    Smit, Wilbert J; Versluis, Jan; Backus, Ellen H G; Bonn, Mischa; Bakker, Huib J

    2018-02-26

    We study the resonant interaction of the OH stretch vibrations of water molecules at the surfaces of liquid water and ice using heterodyne-detected sum-frequency generation (HD-SFG) spectroscopy. By studying different isotopic mixtures of H 2 O and D 2 O, we vary the strength of the interaction, and we monitor the resulting effect on the HD-SFG spectrum of the OH stretch vibrations. We observe that the near-resonant coupling effects are weaker at the surface than in the bulk, both for water and ice, indicating that for both phases of water the OH vibrations are less strongly delocalized at the surface than in the bulk.

  8. Analysis of bromate in drinking water using liquid chromatography-tandem mass spectrometry without sample pretreatment.

    Science.gov (United States)

    Kosaka, Koji; Asami, Mari; Takei, Kanako; Akiba, Michihiro

    2011-01-01

    An analytical method for determining bromate in drinking water was developed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The (18)O-enriched bromate was used as an internal standard. The limit of quantification (LOQ) of bromate was 0.2 µg/L. The peak of bromate was separated from those of coexisting ions (i.e., chloride, nitrate and sulfate). The relative and absolute recoveries of bromate in two drinking water samples and in a synthesized ion solution (100 mg/L chloride, 10 mg N/L nitrate, and 100 mg/L sulfate) were 99-105 and 94-105%, respectively. Bromate concentrations in 11 drinking water samples determined by LC-MS/MS were water without sample pretreatment.

  9. An analysis on water hammer in liquid injection shutdown system of CANDU-9

    International Nuclear Information System (INIS)

    Kim, T. H.; Heo, J.; Han, S. K.; Choi, H. Y.; No, T. S.

    2000-01-01

    The water hammer analysis code, PTRAN, is used for computation of transient pressures and pressure differentials in the Liquid Injection Shutdown System(LISS) piping network of CANDU-9 to ensure that the design allowables for LEVEL C Service Limit are met for the water hammer loads resulting from the water hammer. The LISS piping network of CANDU-9 has incorporated design improvement in considering the water hammer, such as declining the horizontal part of helium header, and raising the elevation of the overall system piping configuration, etc. The maximum pressure in the LISS piping network is found to be 7.92 MPa(a) at the closed valve in the vent line, which is below the allowable working pressure and the valve design pressure under Level C service conditions. And it is also shown that the maximum pressure in CANDU-9 is much lower than that in CANDU-6

  10. LIQUID-LIQUID EQUILIBRIA OF THE TERNARY SYSTEMS PROPIONIC ACID - WATER - SOLVENT (n-AMYL ALCOHOL AND n-AMYL ACETATE

    Directory of Open Access Journals (Sweden)

    Dilek ÖZMEN

    2005-02-01

    Full Text Available The experimental liquid-liquid equilibrium (LLE data have been obtained at 25 oC for ternary systems propionic acid-water-n-amyl alcohol and propionic acid-water-n-amyl acetate. The reliability of the experimental tie line data are checked using the methods of Othmer-Tobias and Hand. The distribution coefficients and separation factors were obtained from experimental results and are also reported. The predicted tie line data obtained by UNIFAC method are compared with experimental data. It is concluded that n-amyl alcohol and n-amyl acetate are suitable separating agents for dilute aqueous propionic acid solutions.

  11. LIQUID-LIQUID EQUILIBRIA OF THE TERNARY SYSTEMS PROPIONIC ACID - WATER - SOLVENT (n-AMYL ALCOHOL AND n-AMYL ACETATE)

    OpenAIRE

    Dilek ÖZMEN

    2005-01-01

    The experimental liquid-liquid equilibrium (LLE) data have been obtained at 25 oC for ternary systems propionic acid-water-n-amyl alcohol and propionic acid-water-n-amyl acetate. The reliability of the experimental tie line data are checked using the methods of Othmer-Tobias and Hand. The distribution coefficients and separation factors were obtained from experimental results and are also reported. The predicted tie line data obtained by UNIFAC method are compared with experimental data. It i...

  12. Steam water cycle chemistry of liquid metal cooled innovative nuclear power reactors

    International Nuclear Information System (INIS)

    Yurmanov, Victor; Lemekhov, Vadim; Smykov, Vladimir

    2012-09-01

    selection of chemistry controls is vital for NPPs with liquid metal cooled reactors. This paper highlights principles and approaches to chemistry controls in steam/water cycles of future NPPs with innovative liquid metal cooled reactors. The recommendations on how to arrange chemistry controls in steam/water cycles of future NPPs with innovative liquid metal cooled reactors are based taking into account: - the experience with operation of fossil power industry; - secondary side water chemistry of lead-bismuth eutectics cooled nuclear reactors at submarines; - steam/water cycles of NPPs with sodium cooled fast breeders BN-350 and BN-600; - secondary water chemistry at conventional NPPs with WER, RBMK and some other reactors. (authors)

  13. Water-clustering in hygroscopic ionic liquids-an implicit solvent analysis.

    Science.gov (United States)

    Maiti, Amitesh; Kumar, Arvind; Rogers, Robin D

    2012-04-21

    Most ionic liquids are known to be hygroscopic to varying degrees, and that can be detrimental or useful depending upon the application in question. Water can accumulate slowly over hours or days to saturation levels corresponding to the humidity level. When designing or deploying a new ionic liquid it is important to be able to estimate its maximum moisture absorbing ability at the temperature and pressure of its operation. With this goal in mind we have carried out computational studies on three ionic liquid systems based on [BF(4)](-), [PF(6)](-), and [Tf(2)N](-) anions and 1-alkyl-3-methyl-imidazolium ([C(n)mim](+)) cations within an implicit solvent formalism. For highly hygroscopic systems like [C(n)mim][BF(4)] we find that non-iterative calculations with single water molecules can lead to significant underestimation of the maximum moisture content, while iterative calculations can result in miscibility behavior qualitatively different from experimental observations. On the other hand, the inclusion of small hydrogen-bonded water-clusters up to an appropriately chosen size is shown to yield better quantitative agreements with experimentally observed water uptake. Additionally, such calculations appear consistent with a number of thermodynamically interesting phase behaviors, including limited-solubility to full-miscibility transitions as a function of temperature and as a function of the alkyl chain length of the imidazolium cation. For hydrophobic systems like [C(n)mim][PF(6)] and [C(n)mim][Tf(2)N] the computed solubility (for each n) is found to have a smooth convergence behavior as a function of the largest cluster-size considered with the results for the larger clusters being close to that obtained by iterative calculations with single water molecules. This journal is © the Owner Societies 2012

  14. Improved prediction of octanol-water partition coefficients from liquid-solute water solubilities and molar volumes

    Science.gov (United States)

    Chiou, C.T.; Schmedding, D.W.; Manes, M.

    2005-01-01

    A volume-fraction-based solvent-water partition model for dilute solutes, in which the partition coefficient shows a dependence on solute molar volume (V??), is adapted to predict the octanol-water partition coefficient (K ow) from the liquid or supercooled-liquid solute water solubility (Sw), or vice versa. The established correlation is tested for a wide range of industrial compounds and pesticides (e.g., halogenated aliphatic hydrocarbons, alkylbenzenes, halogenated benzenes, ethers, esters, PAHs, PCBs, organochlorines, organophosphates, carbamates, and amidesureas-triazines), which comprise a total of 215 test compounds spanning about 10 orders of magnitude in Sw and 8.5 orders of magnitude in Kow. Except for phenols and alcohols, which require special considerations of the Kow data, the correlation predicts the Kow within 0.1 log units for most compounds, much independent of the compound type or the magnitude in K ow. With reliable Sw and V data for compounds of interest, the correlation provides an effective means for either predicting the unavailable log Kow values or verifying the reliability of the reported log Kow data. ?? 2005 American Chemical Society.

  15. The study of water + HCl + ethanol vapor-liquid equilibrium at 78 kPa

    International Nuclear Information System (INIS)

    Ojeda Toro, Juan Carlos; Dobrosz-Gómez, Izabela; Gómez García, Miguel Ángel

    2017-01-01

    Graphical abstract: Comparison between experimental and calculated saturation temperature of water + HCl + ethanol system using two rigorous electrolyte models. - Highlights: • Data for the water + HCl + ethanol VLE is reported at 78 kPa. • The VLE for the system water + HCl + ethanol was determined. • A new set of parameters for extended UNIQUAC model were correlated. • A new set of parameters for LIQUAC model were correlated. - Abstract: In this work, the isobaric vapor-liquid equilibrium (VLE) data obtained for the ternary system water + HCl + ethanol at 78 kPa, using an Ellis still, were studied. Two rigorous electrolyte models (extended UNIQUAC and LIQUAC) were fitted to the experimental data. Ethanol-H + , water-H + , ethanol-Cl − , water-Cl − , and Cl − -H + interaction parameters were determined. Likewise, Henry’s law constants for the volatile electrolyte were defined. A high goodness of fit was obtained for both electrolyte models; however, the extended UNIQUAC one showed better performance (AAD = 0.1326%). Two azeotropes observed in the system were accurately predicted (ethanol + water: x EtOH = 0.86 at 344.6 K; and HCl + water: x HCl = 0.11 at 375.5 K).

  16. Theoretical investigation of the ultrafast dissociation of core-ionized water and uracil molecules immersed in liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Stia, C.R.; Fojon, O.A. [Instituto de Fisica Rosario - CONICET-Universidad Nacional de Rosario, Rosario (Argentina); Gaigeot, M.P. [Laboratoire Analyse et Modelisation pour la Biologie et l' Environnement, LAMBE, UMR-CNRS 8587, Universite d' Evry-Val-d' Essonne, 91 - Evry (France); Institut Universitaire de France, 75 - Paris (France); Vuilleumier, R. [Departement de chimie, Ecole Normale Superieure, 75 - Paris (France); Herve du Penhoat, M.A.; Politis, M.F. [Institut de Mineralogie et de Physique des Milieux Condenses, IMPMC, UMR-CNRS 7590, Universite Pierre et Marie Curie, 75 - Paris (France)

    2010-10-15

    We present a series of ab initio density functional based calculations of the fragmentation dynamics of core-ionized biomolecules. The computations are performed for pure liquid water, aqueous and isolated Uracil. Core ionization is described by replacing the 1s{sup 2} pseudopotential of one atom of the target molecule (C, N or O) with a pseudopotential for a 1s{sup 1} core-hole state. Our results predict that the dissociation of core-ionized water molecules may be reached during the lifetime of inner-shell vacancy (less than 10 fs), leading to OH bond breakage as a primary outcome. We also observe a second fragmentation channel in which total Coulomb explosion of the ionized water molecule occurs. Fragmentation pathways are found similar for pure water or when the water molecule is in the primary hydration shell of the uracil molecule. In the latter case, the proton may be transferred towards the uracil oxygen atoms. When the core hole is located on the uracil molecule, ultrafast dissociation is only observed in the aqueous environment and for nitrogen-K vacancies, resulting in proton transfers towards the hydrogen-bonded water molecule. (authors)

  17. Experimental evidence for the formation of liquid saline water on Mars.

    Science.gov (United States)

    Fischer, Erik; Martínez, Germán M; Elliott, Harvey M; Rennó, Nilton O

    2014-07-16

    Evidence for deliquescence of perchlorate salts has been discovered in the Martian polar region while possible brine flows have been observed in the equatorial region. This appears to contradict the idea that bulk deliquescence is too slow to occur during the short periods of the Martian diurnal cycle during which conditions are favorable for it. We conduct laboratory experiments to study the formation of liquid brines at Mars environmental conditions. We find that when water vapor is the only source of water, bulk deliquescence of perchlorates is not rapid enough to occur during the short periods of the day during which the temperature is above the salts' eutectic value, and the humidity is above the salts' deliquescence value. However, when the salts are in contact with water ice, liquid brine forms in minutes, indicating that aqueous solutions could form temporarily where salts and ice coexist on the Martian surface and in the shallow subsurface. The formation of brines at Martian conditions was studied experimentallyBulk deliquescence from water vapor is too slow to occur diurnally on MarsBrines form in minutes when salts are placed in direct contact with ice.

  18. Water injection into vapor- and liquid-dominated reservoirs: Modeling of heat transfer and mass transport

    Energy Technology Data Exchange (ETDEWEB)

    Pruess, K.; Oldenburg, C.; Moridis, G.; Finsterle, S. [Lawrence Berkeley National Lab., CA (United States)

    1997-12-31

    This paper summarizes recent advances in methods for simulating water and tracer injection, and presents illustrative applications to liquid- and vapor-dominated geothermal reservoirs. High-resolution simulations of water injection into heterogeneous, vertical fractures in superheated vapor zones were performed. Injected water was found to move in dendritic patterns, and to experience stronger lateral flow effects than predicted from homogeneous medium models. Higher-order differencing methods were applied to modeling water and tracer injection into liquid-dominated systems. Conventional upstream weighting techniques were shown to be adequate for predicting the migration of thermal fronts, while higher-order methods give far better accuracy for tracer transport. A new fluid property module for the TOUGH2 simulator is described which allows a more accurate description of geofluids, and includes mineral dissolution and precipitation effects with associated porosity and permeability change. Comparisons between numerical simulation predictions and data for laboratory and field injection experiments are summarized. Enhanced simulation capabilities include a new linear solver package for TOUGH2, and inverse modeling techniques for automatic history matching and optimization.

  19. Enrichment and isotope separation of tritium between hydrogen and liquid water in trikle bed reactor

    International Nuclear Information System (INIS)

    Boumahraz, L.

    1986-09-01

    The tritium produced by ternary fission within pent fuel will be in most part as HTO form in aqueous effluents of the reprocessing plant. Its decharge to the environment will prove detrimental and studies have been undertaken to develop techniques to confine it and process it. For confining tritium in small volumes of aqueous effluents, a special study has been achieved using the ELEX process which should be adapted for use in the design of reprocessing plant. This process is a combination of water electrolysis and tritium exchange between hydrogen and liquid water in contre - courant trikle bed reactor in presence of platined hydrophobic catalyst. Experiments carried out have enabled : demonstration of the effectiveness of platined hydrophobic catalyst in isotope exchange and separation reaction of tritium between hydrogen and liquid water. Development of a pretreatment method of aqueous effluents that have to be detriliated to eliminate impurities which would be detrimental to the ELEX process system by accumulating in the electrolyser and being absorbed in the exchange column. To check hydrodynamical functionment for contre-courant flow system water-hydrogen in trikle bed reactor

  20. The management plan of liquid effluent in Korean advanced light water reactor

    International Nuclear Information System (INIS)

    Kim, S. H.; Lim, H. S.; Jeong, D. W.; Jeong, D. Y.

    2001-01-01

    Non-radioactive liquid effluent in Korean Advanced Light Water Reactor is transferred and treated in centralized waste treatment facility after the radioactivity in effluent is checked within power block. The liquid effluent from centralized waste treatment facility will be discharged by way of discharge canal in order to be in the sufficient condition. As a result of investigating the radiation monitoring design in accordance with 20 provisions by Korean Regulatory Authority, each effluent radiation monitoring with 20 provisions by Korean Regulatory Authority, each effluent radiation monitoring design satisfies the regulatory guideline. In relation to sampling and analyses, most systems satisfy the regulatory guideline except for some effluents from turbine building. And, though sampling and analyses are performed after radioactivity is monitored at each system in turbine building, these exceptions in turbine building effluents are expected to cause no significant problems because radioactivity is monitored by direct or indirect methods prior to release from turbine building. Integrated monitoring on liquid effluent from the centralized waste water treatment facility is not necessary because radiation monitoring, sampling and analyses on each system within power block are performed, and operational effectiveness compared with cost according to adding the radiation monitoring equipment is too low. So, whether the radiation monitoring in this effluent is reflected on design or not is planned to be determined through discussion with regulatory authority

  1. A thermomechanical model for the fragmentation of a liquid metal droplet cooled by water

    Science.gov (United States)

    Ivochkin, Yu P.; Monastyrskiy, V. P.

    2017-11-01

    A thermo mechanical aspect of the fragmentation of a liquid metal droplet, solidified as it falls into cold water, is considered in the presented model. The formation of a solid phase in the form of continuous, fluid-tight and relatively rigid casting skin results in a pressure decrease inside the droplet due to the difference between liquid and solid metal density. Because of the high compression modulus of the melt, the pressure in the droplet becomes negative when the thickness of the solid skin achieves several microns. The tensile stress in the melt results in the deformation of the casting skin or the melt’s continuity violation in the form of a shrinkage pore. The rupture of the deformed solid crust results in the penetration of steam jets into the liquid part of the drop. Due to the difference in pressure in the surrounding steam and in the droplet, the casting skin is crushed and the melt is blown out. Both scenarios contribute to the hydrodynamic destruction of the droplet. The suggested thermo mechanical model gives a qualitative explanation for experimental data. In the experimental part of the work, droplets of molten Sn were solidified in water. The solidified pieces of the droplets usually include deformed, thin-walled shells and dispersed particles. On a qualitative level the composition and shape of the solid fragments can be explained within the bounds of the suggested thermo mechanical model.

  2. Method and apparatus for electrokinetic co-generation of hydrogen and electric power from liquid water microjets

    Science.gov (United States)

    Saykally, Richard J; Duffin, Andrew M; Wilson, Kevin R; Rude, Bruce S

    2013-02-12

    A method and apparatus for producing both a gas and electrical power from a flowing liquid, the method comprising: a) providing a source liquid containing ions that when neutralized form a gas; b) providing a velocity to the source liquid relative to a solid material to form a charged liquid microjet, which subsequently breaks up into a droplet spay, the solid material forming a liquid-solid interface; and c) supplying electrons to the charged liquid by contacting a spray stream of the charged liquid with an electron source. In one embodiment, where the liquid is water, hydrogen gas is formed and a streaming current is generated. The apparatus comprises a source of pressurized liquid, a microjet nozzle, a conduit for delivering said liquid to said microjet nozzle, and a conductive metal target sufficiently spaced from said nozzle such that the jet stream produced by said microjet is discontinuous at said target. In one arrangement, with the metal nozzle and target electrically connected to ground, both hydrogen gas and a streaming current are generated at the target as it is impinged by the streaming, liquid spray microjet.

  3. Liquid and Frozen Storage of Agouti (Dasyprocta leporina) Semen Extended with UHT Milk, Unpasteurized Coconut Water, and Pasteurized Coconut Water.

    Science.gov (United States)

    Mollineau, W M; Adogwa, A O; Garcia, G W

    2010-09-14

    This study evaluated the effects of semen extension and storage on forward progressive motility % (FPM%) in agouti semen. Three extenders were used; sterilized whole cow's milk (UHT Milk), unpasteurized (CW) and pasteurized coconut water (PCW), and diluted to 50, 100, 150, and 200 × 10(6) spermatozoa/ml. Experiment 1: 200 ejaculates were extended for liquid storage at 5(∘)C and evaluated every day for 5 days to determine FPM% and its rate of deterioration. Experiment 2: 150 ejaculates were extended for storage as frozen pellets in liquid nitrogen at -195(∘)C, thawed at 30(∘) to 70(∘)C for 20 to 50 seconds after 5 days and evaluated for FPM% and its rate of deterioration. Samples treated with UHT milk and storage at concentrations of 100 × 10(6) spermatozoa/ml produced the highest means for FPM% and the slowest rates of deterioration during Experiment 1. During Experiment 2 samples thawed at 30(∘)C for 20 seconds exhibited the highest means for FPM% (12.18 ± 1.33%), 85% rate of deterioration. However, samples were incompletely thawed. This was attributed to the diameter of the frozen pellets which was 1 cm. It was concluded that the liquid storage method was better for short term storage.

  4. Discrepancies between two measurements and two model approaches for liquid water flow in snow

    Science.gov (United States)

    Wever, N.; Schmid, L.; Heilig, A.; Fierz, C. G.; Lehning, M.

    2014-12-01

    Liquid water flow in snowpacks is a complicated process to measure or to simulate in snowpack models, although it is important for assessing, for example, soil moisture variations, streamflow discharge or wet snow avalanche formation. The measurement site Weissfluhjoch (WFJ) is equipped with instruments recording meteorological conditions and snowpack properties, including a snow lysimeter and an upward looking ground penetrating radar (upGPR). The upGRP, among other capabilities, is able to track the progress of the melt water front through the seasonal snowpack at WFJ, whereas the snow lysimeter only records liquid water runoff from the snowpack. The 1 dimensional physics-based snowpack model SNOWPACK has recently been extended with a solver for Richards equation, which provides a demonstrable improvement in simulating snowpack runoff, especially on the hourly time scale, when compared to a simpler bucket-type approach. Here, we compare the two measurement methods and the two snowpack simulations for four snow seasons with respect to the progress of the melt water front through the snowpack and snowpack runoff. We show that in the studied period, snowpack runoff in the melt season starts before the arrival of the melt water front at the bottom of the snowpack as detected by the upGPR. This discrepancy is in the order of several days to 1-2 weeks. The agreement between measured and modeled snowpack runoff is higher, although modeled snowpack runoff is still lagging several days from observed runoff, depending on the used water transport scheme. This demonstrates that the early start of snowpack runoff is likely associated with the existence of preferential flow paths. The modeled progress of the melt water front is faster than observed in the upGPR data. This contributes to a better predicition of the onset of snowpack runoff, but may have consequences for the representation of the internal snowpack in the model. The study highlights the extreme difficulties in

  5. Phase equilibria of liquid (water + butyric acid + oleyl alcohol) ternary system

    International Nuclear Information System (INIS)

    Bilgin, Mehmet

    2006-01-01

    (Liquid + liquid) equilibrium (LLE) data for the ternary system of (water + butyric acid + oleyl alcohol) at T = (298.15, 308.15, and 318.15) K are reported. Complete phase diagrams were obtained by determining solubility and the tie-line data. The reliability of the experimental tie lines was confirmed by using Othmer-Tobias correlation. The UNIFAC method was used to predict the phase equilibrium data. The phase diagrams for the ternary mixtures including both the experimental and correlated tie lines are presented. Distribution coefficients and separation factors were evaluated for the immiscibility region. A comparison of the solvent extracting capability was made with respect to distribution coefficients, separation factors, and solvent-free selectivity bases for T = (298.15, 308.15, and 318.15) K. It is concluded that oleyl alcohol may serve as an adequate solvent to extract butyric acid from its dilute aqueous solutions

  6. Phase equilibria of liquid (water + butyric acid + oleyl alcohol) ternary system

    Energy Technology Data Exchange (ETDEWEB)

    Bilgin, Mehmet [Istanbul University, Engineering Faculty, Chemical Engineering Department, 34320 Avcilar, Istanbul (Turkey)]. E-mail: mbilgin@istanbul.edu.tr

    2006-12-15

    (Liquid + liquid) equilibrium (LLE) data for the ternary system of (water + butyric acid + oleyl alcohol) at T = (298.15, 308.15, and 318.15) K are reported. Complete phase diagrams were obtained by determining solubility and the tie-line data. The reliability of the experimental tie lines was confirmed by using Othmer-Tobias correlation. The UNIFAC method was used to predict the phase equilibrium data. The phase diagrams for the ternary mixtures including both the experimental and correlated tie lines are presented. Distribution coefficients and separation factors were evaluated for the immiscibility region. A comparison of the solvent extracting capability was made with respect to distribution coefficients, separation factors, and solvent-free selectivity bases for T = (298.15, 308.15, and 318.15) K. It is concluded that oleyl alcohol may serve as an adequate solvent to extract butyric acid from its dilute aqueous solutions.

  7. A novel mechanism for the extraction of metals from water to ionic liquids.

    Science.gov (United States)

    Janssen, Camiel H C; Sánchez, Antonio; Witkamp, Geert-Jan; Kobrak, Mark N

    2013-11-11

    We present a novel mechanism for the extraction of metals from aqueous phases to room-temperature ionic liquids (ILs) by use of a high-temperature salt as an extraction agent. The mechanism capitalizes on the fact that charged metal complexes are soluble in ILs; this allows for extraction of charged complexes rather than the neutral species, which are formed by conventional approaches. The use of a well-chosen extraction agent also suppresses the competing ion-exchange mechanism, thus preventing degradation of the ionic liquid. The approach permits the use of excess extractant to drive the recovery of metals in high yield. This work presents both a thermodynamic framework for understanding the approach and experimental verification of the process in a range of different ILs. The method has great potential value in the recovery of metals, water purification and nuclear materials processing. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. Measurement of capacity coefficient of inclined liquid phase catalytic exchange column for tritiated water processing

    International Nuclear Information System (INIS)

    Yamai, Hideki; Konishi, Satoshi; Yamanishi, Toshihiko; Okuno, Kenji

    1994-01-01

    Liquid phase catalytic exchange (LPCE) is effective method for enrichment and removal of tritium from tritiated water. Capacity coefficients of operating LPCE column that are essential to evaluate column performance were measured. Experiments were performed with short catalyst packed columns and effect of inclination was studied. Method for evaluation of capacity coefficients was established from measurement of isotope concentration of liquid, vapor, gas phases at the two ends of the column. The capacity coefficients were measured under various superficial gas velocities. Feasibility study of helical columns with roughened inner surface was performed with short inclined columns. The column performance was not strongly affected by the inclination. The result indicates technological feasibility of helical LPCE column, that is expected to have operation stability and reduced height

  9. Advantages of liquid fluoride thorium reactor in comparison with light water reactor

    Energy Technology Data Exchange (ETDEWEB)

    Bahri, Che Nor Aniza Che Zainul, E-mail: anizazainul@gmail.com; Majid, Amran Ab.; Al-Areqi, Wadeeah M. [Nuclear Science Program, School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor (Malaysia)

    2015-04-29

    Liquid Fluoride Thorium Reactor (LFTR) is an innovative design for the thermal breeder reactor that has important potential benefits over the traditional reactor design. LFTR is fluoride based liquid fuel, that use the thorium dissolved in salt mixture of lithium fluoride and beryllium fluoride. Therefore, LFTR technology is fundamentally different from the solid fuel technology currently in use. Although the traditional nuclear reactor technology has been proven, it has perceptual problems with safety and nuclear waste products. The aim of this paper is to discuss the potential advantages of LFTR in three aspects such as safety, fuel efficiency and nuclear waste as an alternative energy generator in the future. Comparisons between LFTR and Light Water Reactor (LWR), on general principles of fuel cycle, resource availability, radiotoxicity and nuclear weapon proliferation shall be elaborated.

  10. Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water

    Directory of Open Access Journals (Sweden)

    Leqin He

    2014-05-01

    Full Text Available Quaternary ammonium geminal Brønsted acid ionic liquids (GBAILs based on zwitterionic 1,2-bis[N-methyl-N-(3-sulfopropyl-alkylammonium]ethane (where the carbon number of the alkyl chain is 4, 8, 10, 12, 14, 16, or 18 and p-toluenesulfonic acid monohydrate were synthesized. The catalytic ionic liquids were applied in three-component Mannich reactions with an aldehyde, ketone, and amine at 25 °C in water. The effects of the type and amount of catalyst and reaction time as well as the scope of the reaction were investigated. Results showed that GBAIL-C14 has excellent catalytic activity and fair reusability. The catalytic procedure was simple, and the catalyst could be recycled seven times via a simple separation process without noticeable decreases in catalytic activity.

  11. Geminal Brønsted acid ionic liquids as catalysts for the Mannich reaction in water.

    Science.gov (United States)

    He, Leqin; Qin, Shenjun; Chang, Tao; Sun, Yuzhuang; Zhao, Jiquan

    2014-05-15

    Quaternary ammonium geminal Brønsted acid ionic liquids (GBAILs) based on zwitterionic 1,2-bis[N-methyl-N-(3-sulfopropyl)-alkylammonium]ethane (where the carbon number of the alkyl chain is 4, 8, 10, 12, 14, 16, or 18) and p-toluenesulfonic acid monohydrate were synthesized. The catalytic ionic liquids were applied in three-component Mannich reactions with an aldehyde, ketone, and amine at 25 °C in water. The effects of the type and amount of catalyst and reaction time as well as the scope of the reaction were investigated. Results showed that GBAIL-C14 has excellent catalytic activity and fair reusability. The catalytic procedure was simple, and the catalyst could be recycled seven times via a simple separation process without noticeable decreases in catalytic activity.

  12. Scattering data for modelling positron tracks in gaseous and liquid water

    International Nuclear Information System (INIS)

    Blanco, F; Roldán, A M; Krupa, K; García, G; McEachran, R P; Machacek, J R; Buckman, S J; Sullivan, J P; White, R D; Marjanović, S; Petrović, Z Lj; Brunger, M J; Chiari, L; Limão-Vieira, P

    2016-01-01

    We present in this study a self-consistent set of scattering cross sections for positron collisions with water molecules, in the energy range 0.1–10 000 eV, with the prime motivation being to provide data for modelling purposes. The structure of the database is based on a new model potential calculation, including interference terms, which provides differential and integral elastic as well as integral inelastic positron scattering cross sections for water molecules over the whole energy range considered here. Experimental and theoretical data available in the literature have been integrated into the database after a careful analysis of their uncertainties and their self-consistency. These data have been used as input parameters for a step-by-step Monte Carlo simulation procedure, providing valuable information on energy deposition, positron range, and the relative percentages of specific interactions (e.g. positronium formation, direct ionisation, electronic, vibrational and rotational excitations) in gaseous and liquid water. (paper)

  13. Phase transitions on (liquid + liquid) equilibria for (water + 1-methylnaphthalene + light aromatic hydrocarbon) ternary systems at T = (563, 573, and 583) K

    International Nuclear Information System (INIS)

    Togo, Masaki; Inamori, Yoshiki; Shimoyama, Yusuke

    2012-01-01

    Highlights: ► Mixtures of (water + 1-methylnaphthalene + light aromatic hydrocarbon) are focused. ► Phase transition pressures on (liquid + liquid) equilibria were measured. ► Effects of aromatic hydrocarbons on phase transition pressure are investigated. ► Phase transition pressures are discussed using dielectric constants of hydrocarbons. - Abstract: Phase transitions for (water + 1-methylnaphthalene + light aromatic hydrocarbon) ternary systems are observed at their (liquid + liquid) equilibria at T = (563, 573, and 583) K and (8.6 to 25.0) MPa. The phase transition pressures at T = (563, 573, and 583) K were measured for the five species of light aromatic hydrocarbons, o-, m-, p-xylenes, ethylbenzene, and mesitylene. The measurements of the phase transition pressures were carried out by changing the feed mole fraction of water and 1-methylnaphthalene in water free, respectively. Effects of the feed mole fraction of water on the phase transition pressures are very small. Increasing the feed mole fraction of 1-methylnaphthalene results in decreasing the phase transition pressures at constant temperature. The slopes depending on the feed mole fraction for 1-methylnaphthalene at the phase transition pressures are decreased with increasing temperature for (water + 1-methylnaphthalene + p-xylene), (water + 1-methylnaphthalene + o-xylene), and (water + 1-methylnaphthalene + mesitylene) systems. For xylene isomers, the highest and lowest of the phase transition pressures are obtained in the case of p- and o-xylenes, respectively. The phase transition pressures for ethylbenzene are lower than those in the case of p-xylene. The similar phase transition pressures are given for p-xylene and mesitylene.

  14. Research on Liquid Management Technology in Water Tank and Reactor for Propulsion System with Hydrogen Production System Utilizing Aluminum and Water Reaction

    Science.gov (United States)

    Imai, Ryoji; Imamura, Takuya; Sugioka, Masatoshi; Higashino, Kazuyuki

    2017-12-01

    High pressure hydrogen produced by aluminum and water reaction is considered to be applied to space propulsion system. Water tank and hydrogen production reactor in this propulsion system require gas and liquid separation function under microgravity condition. We consider to install vane type liquid acquisition device (LAD) utilizing surface tension in the water tank, and install gas-liquid separation mechanism by centrifugal force which swirling flow creates in the hydrogen reactor. In water tank, hydrophilic coating was covered on both tank wall and vane surface to improve wettability. Function of LAD in water tank and gas-liquid separation in reaction vessel were evaluated by short duration microgravity experiments using drop tower facility. In the water tank, it was confirmed that liquid was driven and acquired on the outlet due to capillary force created by vanes. In addition of this, it was found that gas-liquid separation worked well by swirling flow in hydrogen production reactor. However, collection of hydrogen gas bubble was sometimes suppressed by aluminum alloy particles, which is open problem to be solved.

  15. Water-based synthesis of hydrophobic ionic liquids for high-energy electrochemical devices

    International Nuclear Information System (INIS)

    Montanino, Maria; Alessandrini, Fabrizio; Passerini, Stefano; Appetecchi, Giovanni Battista

    2013-01-01

    Highlights: ► Water-based synthesis of ionic liquids with high yield. ► Full recycling of reagents. ► High purity pyrrolidinium-based ionic liquids with exceptional electrochemical stability window. ► Lithium plating from pyrrolidinium-based ionic liquids. -- Abstract: In this work is described an innovative synthesis route for hydrophobic ionic liquids (ILs) composed of N-methyl-N-alkylpyrrolidinium (or piperidinium) or imidazolium or tetralkylammonium cations and (perfluoroalkylsulfonyl)imide, ((C n F 2n+1 SO 2 )(C m F 2m+1 SO 2 )N − ), anions. This synthesis does not require the use of any environmental unfriendly solvent such as acetone, acetonitrile or halogen-containing compounds, which is not welcome in industrial applications. Only water is used as the process solvent throughout the entire process. In addition, the commonly used iodine-containing reagents were replaced by the cheaper, more chemically stable and less toxic bromine-containing compounds. A particular care was devoted to the development of the purification route, which is especially important for ILs to be used in high-energy electrochemical devices such as high voltage supercapacitors and lithium batteries. The effect of the reaction temperature, the time and the stoichiometry in the various steps of the synthesis have been investigated in detail. This novel procedure allowed obtaining ultrapure (>99.9 wt.%), clear, colourless, inodorous ILs with an overall yield above 92 wt.% and moisture content below 1 ppm. NMR measurements were run to confirm the chemical structure whereas elemental analysis and electrochemical tests were performed to check the purity of the synthesized ILs

  16. Ice versus liquid water saturation in simulations of the indian summer monsoon

    Science.gov (United States)

    Glazer, Russell H.; Misra, Vasubandhu

    2018-02-01

    At the same temperature, below 0 °C, the saturation vapor pressure (SVP) over ice is slightly less than the SVP over liquid water. Numerical models use the Clausius-Clapeyron relation to calculate the SVP and relative humidity, but there is not a consistent method for the treatment of saturation above the freezing level where ice and mixed-phase clouds may be present. In the context of current challenges presented by cloud microphysics in climate models, we argue that a better understanding of the impact that this treatment has on saturation-related processes like cloud formation and precipitation, is needed. This study explores the importance of the SVP calculation through model simulations of the Indian summer monsoon (ISM) using the regional spectral model (RSM) at 15 km grid spacing. A combination of seasonal and multiyear simulations is conducted with two saturation parameterizations. In one, the SVP over liquid water is prescribed through the entire atmospheric column (woIce), and in another the SVP over ice is used above the freezing level (wIce). When SVP over ice is prescribed, a thermodynamic drying of the middle and upper troposphere above the freezing level occurs due to increased condensation. In the wIce runs, the model responds to the slight decrease in the saturation condition by increasing, relative to the SVP over liquid water only run, grid-scale condensation of water. Increased grid-scale mean seasonal precipitation is noted across the ISM region in the simulation with SVP over ice prescribed. Modification of the middle and upper troposphere moisture results in a decrease in mean seasonal mid-level cloud amount and an increase in high cloud amount when SVP over ice is prescribed. Multiyear simulations strongly corroborate the qualitative results found in the seasonal simulations regarding the impact of ice versus liquid water SVP on the ISM's mean precipitation and moisture field. The mean seasonal rainfall difference over All India between w

  17. Clean water billing monitoring system using flow liquid meter sensor and SMS gateway

    Science.gov (United States)

    Fahmi, F.; Hizriadi, A.; Khairani, F.; Andayani, U.; Siregar, B.

    2018-03-01

    Public clean water company (PDAM) as a public service is designed and organized to meet the needs of the community. Currently, the number of PDAM subscribers is very big and will continue to grow, but the service and facilities to customers are still done conventionally by visiting the customer’s home to record the last position of the meter. One of the problems of PDAM is the lack of disclosure of PDAM customers’ invoice because it is only done monthly. This, of course, makes PDAM customers difficult to remember the date of payment of water account. Therefore it is difficult to maintain the efficiency. The purpose of this research is to facilitate customers of PDAM water users to know the details of water usage and the time of payment of water bills easily. It also facilitates customers in knowing information related to the form of water discharge data used, payment rates, and time grace payments using SMS Gateway. In this study, Flow Liquid Meter Sensor was used for data retrieval of water flowing in the piping system. Sensors used to require the help of Hall Effect sensor that serves to measure the speed of water discharge and placed on the pipe that has the same diameter size with the sensor diameter. The sensor will take the data from the rate of water discharge it passes; this data is the number of turns of the mill on the sensor. The results of the tests show that the built system works well in helping customers know in detail the amount of water usage in a month and the bill to be paid

  18. Mechanism for migration of light nonaqueous phase liquids beneath the water table

    International Nuclear Information System (INIS)

    Krueger, J.P.; Portman, M.E.

    1991-01-01

    This paper reports on an interesting transport mechanism may account for the presence of light nonaqueous phase liquid (LNAPL) found beneath the water table in fine-grained aquifers. During the course of two separate site investigations related to suspected releases from underground petroleum storage tanks, LNAPL was found 7 to 10 feet below the regional water table. In both cases, the petroleum was present within a sand seam which was encompassed within a deposit of finer-grained sediments. The presence of LNAPL below the water table is uncommon; typically, LNAPL is found floating on the water table or on the capillary fringe. The occurrence of LNAPL below the water table could have resulted from fluctuating regional water levels which allowed the petroleum to enter the sand when the water table was a lower stage or, alternately, could have occurred as a result of the petroleum depressing the water table beneath the level of the sand. In fine-grained soils where the lateral migration rate is low, the infiltrating LNAPL may depress the water table to significant depth. The LNAPL may float on the phreatic surface with the bulk of its volume beneath the phreatic surface. Once present in the sand and surrounded by water-saturated fine-grained sediments, capillary forces prevent the free movement of the petroleum back across the boundary from the coarse-grained sediments to the fine-grained sediments. Tapping these deposits with a coarser grained filter packed monitoring well releases the LNAPL, which may accumulate to considerable thickness in the monitoring well

  19. Measuring Snow Liquid Water Content with Low-Cost GPS Receivers

    Science.gov (United States)

    Koch, Franziska; Prasch, Monika; Schmid, Lino; Schweizer, Jürg; Mauser, Wolfram

    2014-01-01

    The amount of liquid water in snow characterizes the wetness of a snowpack. Its temporal evolution plays an important role for wet-snow avalanche prediction, as well as the onset of meltwater release and water availability estimations within a river basin. However, it is still a challenge and a not yet satisfyingly solved issue to measure the liquid water content (LWC) in snow with conventional in situ and remote sensing techniques. We propose a new approach based on the attenuation of microwave radiation in the L-band emitted by the satellites of the Global Positioning System (GPS). For this purpose, we performed a continuous low-cost GPS measurement experiment at the Weissfluhjoch test site in Switzerland, during the snow melt period in 2013. As a measure of signal strength, we analyzed the carrier-to-noise power density ratio (C/N0) and developed a procedure to normalize these data. The bulk volumetric LWC was determined based on assumptions for attenuation, reflection and refraction of radiation in wet snow. The onset of melt, as well as daily melt-freeze cycles were clearly detected. The temporal evolution of the LWC was closely related to the meteorological and snow-hydrological data. Due to its non-destructive setup, its cost-efficiency and global availability, this approach has the potential to be implemented in distributed sensor networks for avalanche prediction or basin-wide melt onset measurements. PMID:25384007

  20. {sup 222}Rn determination in water and brine samples using liquid scintillation spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Thiago C.; Oliveira, Arno H., E-mail: oliveiratco2010@gmail.com [Universidade Federal de Minas Gerais (DEN/UFMG), Belo Horizonte (Brazil). Departamento de Engenharia Nuclear; Monteiro, Roberto P.G.; Moreira, Rubens M., E-mail: rpgm@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN-CNEN-MG), Belo Horizonte, MG (Brazil)

    2017-07-01

    Liquid scintillation spectrometry (LSC) is the most common technique used for {sup 222}Rn determination in environmental aqueous sample. In this study, the performance of water-miscible (Ultima Gold AB) and immiscible (Optiscint) liquid scintillation cocktails has been compared for different matrices. {sup 241}Am, {sup 90}Sr and {sup 226}Ra standard solutions were used for LSC calibration. {sup 214}Po region was defined as better for both cocktails. Counting efficiency of 76 % and optimum PSA level of 95 for Ultima Gold AB cocktail, and counting efficiency of 82 % and optimum PSA level of 85 for Optiscint cocktail were obtained. Both cocktails showed similar results when applied for {sup 222}Rn activity determination in water and brine samples. However the Optiscint is recommended due to its quenching resistance. Limit of detection of 0.08 and 0.06 Bq l{sup -1} were obtained for water samples using a sample:cocktail ratio of 10:12 mL for Ultima Gold AB and Optiscint cocktails, respectively. Limit of detection of 0.08 and 0.04 Bq l{sup -1} were obtained for brine samples using a sample:cocktail ratio of 8:12 mL for Ultima Gold AB and Optiscint cocktails, respectively. (author)

  1. Measuring Snow Liquid Water Content with Low-Cost GPS Receivers

    Directory of Open Access Journals (Sweden)

    Franziska Koch

    2014-11-01

    Full Text Available The amount of liquid water in snow characterizes the wetness of a snowpack. Its temporal evolution plays an important role for wet-snow avalanche prediction, as well as the onset of meltwater release and water availability estimations within a river basin. However, it is still a challenge and a not yet satisfyingly solved issue to measure the liquid water content (LWC in snow with conventional in situ and remote sensing techniques. We propose a new approach based on the attenuation of microwave radiation in the L-band emitted by the satellites of the Global Positioning System (GPS. For this purpose, we performed a continuous low-cost GPS measurement experiment at the Weissfluhjoch test site in Switzerland, during the snow melt period in 2013. As a measure of signal strength, we analyzed the carrier-to-noise power density ratio (C/N0 and developed a procedure to normalize these data. The bulk volumetric LWC was determined based on assumptions for attenuation, reflection and refraction of radiation in wet snow. The onset of melt, as well as daily melt-freeze cycles were clearly detected. The temporal evolution of the LWC was closely related to the meteorological and snow-hydrological data. Due to its non-destructive setup, its cost-efficiency and global availability, this approach has the potential to be implemented in distributed sensor networks for avalanche prediction or basin-wide melt onset measurements.

  2. Analysis of trace dicyandiamide in stream water using solid phase extraction and liquid chromatography UV spectrometry.

    Science.gov (United States)

    Qiu, Huidong; Sun, Dongdi; Gunatilake, Sameera R; She, Jinyan; Mlsna, Todd E

    2015-09-01

    An improved method for trace level quantification of dicyandiamide in stream water has been developed. This method includes sample pretreatment using solid phase extraction. The extraction procedure (including loading, washing, and eluting) used a flow rate of 1.0mL/min, and dicyandiamide was eluted with 20mL of a methanol/acetonitrile mixture (V/V=2:3), followed by pre-concentration using nitrogen evaporation and analysis with high performance liquid chromatography-ultraviolet spectroscopy (HPLC-UV). Sample extraction was carried out using a Waters Sep-Pak AC-2 Cartridge (with activated carbon). Separation was achieved on a ZIC(®)-Hydrophilic Interaction Liquid Chromatography (ZIC-HILIC) (50mm×2.1mm, 3.5μm) chromatography column and quantification was accomplished based on UV absorbance. A reliable linear relationship was obtained for the calibration curve using standard solutions (R(2)>0.999). Recoveries for dicyandiamide ranged from 84.6% to 96.8%, and the relative standard deviations (RSDs, n=3) were below 6.1% with a detection limit of 5.0ng/mL for stream water samples. Copyright © 2015. Published by Elsevier B.V.

  3. [Detecting Thallium in Water Samples using Dispersive Liquid Phase Microextraction-Graphite Furnace Atomic Absorption Spectroscopy].

    Science.gov (United States)

    Zhu, Jing; Li, Yan; Zheng, Bo; Tang, Wei; Chen, Xiao; Zou, Xiao-li

    2015-11-01

    To develope a method of solvent demulsification dispersive liquid phase microextraction (SD-DLPME) based on ion association reaction coupled with graphite furnace atomic absorption spectroscopy (GFAAS) for detecting thallium in water samples. Methods Thallium ion in water samples was oxidized to Tl(III) with bromine water, which reacted with Cl- to form TlCl4-. The ionic associated compound with trioctylamine was obtained and extracted. DLPME was completed with ethanol as dispersive solvent. The separation of aqueous and organic phase was achieved by injecting into demulsification solvent without centrifugation. The extractant was collected and injected into GFAAS for analysis. With palladium colloid as matrix modifier, a two step drying and ashing temperature programming process was applied for high precision and sensitivity. The linear range was 0.05-2.0 microg/L, with a detection limit of 0.011 microg/L. The relative standard derivation (RSD) for detecting Tl in spiked water sample was 9.9%. The spiked recoveries of water samples ranged from 94.0% to 103.0%. The method is simple, sensitive and suitable for batch analysis of Tl in water samples.

  4. Interactions between drops of a molten aluminum-lithium alloy and liquid water

    International Nuclear Information System (INIS)

    Nelson, L.S.

    1994-01-01

    In certain hypothesized nuclear reactor accident scenarios, 1- to 10-g drops of molten aluminum-lithium alloys might contact liquid water. Because vigorous steam explosions have occurred when large amounts of molten aluminum-lithium alloys were released into water or other coolants, it becomes important to know whether there will be explosions if smaller amounts of these molten alloys similarly come into contact with water. Therefore, the authors released drops of molten Al-3.1 wt pct Li alloy into deionized water at room temperature. The experiments were performed at local atmospheric pressure (0.085 MPa) without pressure transient triggers applied to the water. The absence of these triggers allowed them to (a) investigate whether spontaneous initiation of steam explosions would occur with these drops and (b) study the alloy-water chemical reactions. The drop sizes and melt temperatures were chosen to simulate melt globules that might form during the hypothesized melting of the aluminum-lithium alloy components

  5. Extraction of triazole fungicides in environmental waters utilizing poly (ionic liquid)-functionalized magnetic adsorbent.

    Science.gov (United States)

    Liu, Cheng; Liao, Yingmin; Huang, Xiaojia

    2017-11-17

    This work prepared a new poly (ionic liquid)-functionalized magnetic adsorbent (PFMA) for the extraction of triazole fungicides (TFs) in environmental waters prior to determination by high performance liquid chromatography/diode array detection (HPLC-DAD). A polymerizable ionic liquid, 1-methyl-3-allylimidazolium bis(trifluoromethylsulfonyl)imide was employed to copolymerize with divinylbenzene on the surface of modified magnetite to fabricate the PFMA. The morphology, spectroscopic and magnetic properties of the new adsorbent were investigated by different techniques. A series of key parameters that influence the extraction performance including the amount of PFMA, desorption solvent, adsorption and desorption time, sample pH value and ionic strength were optimized in detail. Under the optimum conditions, the prepared PFMA could extract targeted TFs effectively and quickly under the format of magnetic solid-phase extraction (MSPE). Satisfactory linearities were achieved in the range of 0.1-200.0μg/L for triadimenol and 0.05-200.0μg/L for other TFs with good coefficients of determination above 0.99 for all analytes. The limits of detection (S/N=3) and limits of quantification (S/N=10) for TFs were in the range of 0.0050-0.0078μg/L and 0.017-0.026μg/L, respectively. Environmental waters including lake, river and well waters were used to demonstrate the applicability of developed MSPE-HPLC-DAD method, and satisfactory recoveries and repeatability were obtained. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. The effect of cloud liquid water on tropospheric temperature retrievals from microwave measurements

    Directory of Open Access Journals (Sweden)

    L. Bernet

    2017-11-01

    Full Text Available Microwave radiometry is a suitable technique to measure atmospheric temperature profiles with high temporal resolution during clear sky and cloudy conditions. In this study, we included cloud models in the inversion algorithm of the microwave radiometer TEMPERA (TEMPErature RAdiometer to determine the effect of cloud liquid water on the temperature retrievals. The cloud models were built based on measurements of cloud base altitude and integrated liquid water (ILW, all performed at the aerological station (MeteoSwiss in Payerne (Switzerland. Cloud base altitudes were detected using ceilometer measurements while the ILW was measured by a HATPRO (Humidity And Temperature PROfiler radiometer. To assess the quality of the TEMPERA retrieval when clouds were considered, the resulting temperature profiles were compared to 2 years of radiosonde measurements. The TEMPERA instrument measures radiation at 12 channels in the frequency range from 51 to 57 GHz, corresponding to the left wing of the oxygen emission line complex. When the full spectral information with all the 12 frequency channels was used, we found a marked improvement in the temperature retrievals after including a cloud model. The chosen cloud model influenced the resulting temperature profile, especially for high clouds and clouds with a large amount of liquid water. Using all 12 channels, however, presented large deviations between different cases, suggesting that additional uncertainties exist in the lower, more transparent channels. Using less spectral information with the higher, more opaque channels only also improved the temperature profiles when clouds where included, but the influence of the chosen cloud model was less important. We conclude that tropospheric temperature profiles can be optimized by considering clouds in the microwave retrieval, and that the choice of the cloud model has a direct impact on the resulting temperature profile.

  7. The effect of cloud liquid water on tropospheric temperature retrievals from microwave measurements

    Science.gov (United States)

    Bernet, Leonie; Navas-Guzmán, Francisco; Kämpfer, Niklaus

    2017-11-01

    Microwave radiometry is a suitable technique to measure atmospheric temperature profiles with high temporal resolution during clear sky and cloudy conditions. In this study, we included cloud models in the inversion algorithm of the microwave radiometer TEMPERA (TEMPErature RAdiometer) to determine the effect of cloud liquid water on the temperature retrievals. The cloud models were built based on measurements of cloud base altitude and integrated liquid water (ILW), all performed at the aerological station (MeteoSwiss) in Payerne (Switzerland). Cloud base altitudes were detected using ceilometer measurements while the ILW was measured by a HATPRO (Humidity And Temperature PROfiler) radiometer. To assess the quality of the TEMPERA retrieval when clouds were considered, the resulting temperature profiles were compared to 2 years of radiosonde measurements. The TEMPERA instrument measures radiation at 12 channels in the frequency range from 51 to 57 GHz, corresponding to the left wing of the oxygen emission line complex. When the full spectral information with all the 12 frequency channels was used, we found a marked improvement in the temperature retrievals after including a cloud model. The chosen cloud model influenced the resulting temperature profile, especially for high clouds and clouds with a large amount of liquid water. Using all 12 channels, however, presented large deviations between different cases, suggesting that additional uncertainties exist in the lower, more transparent channels. Using less spectral information with the higher, more opaque channels only also improved the temperature profiles when clouds where included, but the influence of the chosen cloud model was less important. We conclude that tropospheric temperature profiles can be optimized by considering clouds in the microwave retrieval, and that the choice of the cloud model has a direct impact on the resulting temperature profile.

  8. Study of Aerosol Liquid Water Content based on Hygroscopicity Measurements at High Relative Humidity in the North China Plain

    Science.gov (United States)

    Bian, Y.; Zhao, C.

    2013-12-01

    Aerosol has significant effects on direct/indirect climate forcing, visibility, tropospheric chemistry and human health. Water can represent an extensive proportion of the mass of aerosol particles, and can also serve as a medium for aqueous-phase reactions in such particulate matter. In this study, a new method is proposed to estimate the aerosol liquid water content at high relative humidity, based on aerosol hygroscopic growth factors, particle number size distribution and relative humidity measured during the Haze in China (HaChi) campaign of July-August, 2009. The aerosol liquid water content estimated by this method is compared to the results calculated by a thermodynamic equilibrium model (ISORROPIA II). The calculation results from these two methods agree well at high relative humidity above 60% with the correlation coefficient of 0.9658. At relative humidity lower than 60%, the thermodynamic equilibrium model underestimates the aerosol liquid water content. The discrepancy is mainly caused by the ISORROPIA II model, which considers only limited chemical species. The mean and maximum value of aerosol liquid water content during July-August, 2009 in the North China Plain reached 1.69×10^{-4}g/m^3 and 9.71×10^{-4}g/m^3, respectively. Aerosol liquid water content is highly related to the relative humidity. There exists a distinct diurnal variation of the aerosol liquid water content, with lower values during daytime and higher ones during night time. The contribution to the aerosol liquid water content from the accumulation mode is dominating among all the aerosol particle modes.

  9. Empirical Relations for Optical Attenuation Prediction from Liquid Water Content of Fog

    Directory of Open Access Journals (Sweden)

    M. S. Khan

    2012-09-01

    Full Text Available Simultaneous measurements of the liquid water content (LWC and optical attenuation have been analyzed to predict optical attenuation caused by fog particles. Attenuation has been measured at two different wavelengths, 830 nm and 1550 nm, across co-located links. Five months measured data have been processed to assess power-law empirical models, which estimate optical attenuation from the LWC. The proposed models are compared with other published models and are demonstrated to perform sufficiently well to predict optical attenuation if the LWC values are available.

  10. Reaction of water vapour with a clean liquid uranium surface. Revised 1

    International Nuclear Information System (INIS)

    McLean, W. II; Siekhaus, W.

    1986-01-01

    To study the reaction of water vapour with uranium, we have exposed clean liquid uranium surfaces to H 2 O under UHV conditions. We have measured the surface concentration of oxygen as a function of exposure, and determined the maximum attainable surface oxygen concentration X/sup s//sub O/ as a function of temperature. We have used these measurements to estimate, close to the melting point, the solubility of oxygen (X/sup b//sub O/, -4 ) and its surface segregation coefficient β/sup s/(> 10 3 ). 11 refs., 5 figs

  11. Geant4-DNA simulation of electron slowing-down spectra in liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Incerti, S., E-mail: sebastien.incerti@tdt.edu.vn [Division of Nuclear Physics, Ton Duc Thang University, Tan Phong Ward, District 7, Ho Chi Minh City (Viet Nam); Faculty of Applied Sciences, Ton Duc Thang University, Tan Phong Ward, District 7, Ho Chi Minh City (Viet Nam); Univ. Bordeaux, CENBG, UMR 5797, F-33170, Gradignan (France); CNRS, IN2P3, CENBG, UMR 5797, F-33170 Gradignan (France); Kyriakou, I. [Medical Physics Laboratory, University of Ioannina Medical School, 45110 Ioannina (Greece); Tran, H.N. [Division of Nuclear Physics, Ton Duc Thang University, Tan Phong Ward, District 7, Ho Chi Minh City (Viet Nam); Faculty of Applied Sciences, Ton Duc Thang University, Tan Phong Ward, District 7, Ho Chi Minh City (Viet Nam)

    2017-04-15

    This work presents the simulation of monoenergetic electron slowing-down spectra in liquid water by the Geant4-DNA extension of the Geant4 Monte Carlo toolkit (release 10.2p01). These spectra are simulated for several incident energies using the most recent Geant4-DNA physics models, and they are compared to literature data. The influence of Auger electron production is discussed. For the first time, a dedicated Geant4-DNA example allowing such simulations is described and is provided to Geant4 users, allowing further verification of Geant4-DNA track structure simulation capabilities.

  12. Electrochemical assessment of water|ionic liquid biphasic systems towards cesium extraction from nuclear waste

    International Nuclear Information System (INIS)

    Stockmann, T. Jane; Zhang, Jing; Montgomery, Anne-Marie; Ding, Zhifeng

    2014-01-01

    Highlights: • Electroanalytical chemistry was employed to assess cesium ion extraction in biphasic systems. • Water|ionic liquid systems are much more efficient than traditional water|organic ones. • The metal ion to ligand stoichiometry and overall complexation constant were determined. • The stoichiometry was confirmed by mass spectrometry. • The ligand CMPO used in TRUEX processes was found to be effective for the FIT. - Abstract: A room temperature ionic liquid (IL) composed of a quaternary alkylphosphonium (trihexyltetradecylphosphonium, P 66614 + ) and tetrakis(pentafluorophenyl)borate anion (TB − ) was employed within a water|P 66614 TB (w|P 66614 TB or w|IL) biphasic system to evaluate cesium ion extraction in comparison to that with a traditional water|organic solvent (w|o) combination. 137 Cs is a major contributor to the radioactivity of spent nuclear fuel as it leaves the reactor, and its extraction efficiency is therefore of considerable importance. The extraction was facilitated by the ligand octyl(phenyl)-N,N′-diisobutylcarbamoylphosphine oxide (CMPO) used in TRans-Uranium EXtraction processes and investigated through well established liquid|liquid electrochemistry. This study gave access to the metal ion to ligand (1:n) stoichiometry and overall complexation constant, β, of the interfacial complexation reaction which were determined to be 1:3 and 1.6 × 10 11 at the w|P 66614 TB interface while the study at w|o elicited an n equal to 1 with β equal to 86.5. Through a straightforward relationship, these complexation constant values were converted to distribution coefficients, δ α , with the ligand concentrations studied for comparison to other studies present in the literature; the w|o and w|IL systems gave δ α of 2 and 8.2 × 10 7 , respectively, indicating a higher overall extraction efficiency for the latter. For the w|o system, the metal ion-ligand stoichiometries were confirmed through isotopic distribution analysis of mass

  13. Enhancing efficiency of using water due to explosive breakup of liquid drop

    Directory of Open Access Journals (Sweden)

    Borisova Anastasia G.

    2017-01-01

    Full Text Available Using high-speed video recording, the experiments were performed to research quantitative characteristics of explosive breakup phenomenon of 5–15 μl water droplets containing 2×2×1 mm and 2×2×2 mm solid inclusions, when heated in a tube furnace at temperatures of 1070–1370 K. Experimental results report number and size of the droplets detached during explosive breakup. We show that the fragmentation of liquid layer covering solid particles facilitates the increase the evaporation surface area 15-fold versus the initial surface area of a drop.

  14. Preconcentration procedure using vortex-assisted liquid-liquid microextraction for the fast determination of trace levels of thorium in water samples

    International Nuclear Information System (INIS)

    Ehsan Zolfonoun; Maryam Salahinejad

    2013-01-01

    A new simple and rapid vortex-assisted liquid-liquid microextraction method was applied for the determination of thorium in water samples. In this method, chloroform used as extraction solvent was directly injected into the water sample solution. The extraction solvent was dispersed into the aqueous phase under vigorously shaking with the vortex. After centrifuging, the fine droplets of extractant phase were settled to the bottom of the conical-bottom centrifuge tube. The effect of different experimental parameters on the performance of the method were studied and discussed. Under the optimum conditions, the detection limit for Th(IV) was 7.5 ng mL -1 . The precision of the method, evaluated as the relative standard deviation obtained by analyzing of 10 replicates, was 2.8 %. The practical applicability of the developed method was examined using natural water and monazite sand samples. (author)

  15. Dentin wear after simulated toothbrushing with water, a liquid dentifrice or a standard toothpaste.

    Science.gov (United States)

    Jang, Youngjune; Ihm, Jung-joon; Baik, Su-jin; Yoo, Kyung-jin; Jang, Da-hyun; Roh, Byoung-duck; Seo, Deog-gyu

    2015-12-01

    To investigate the influence of dentifrices with and without abrasives on the wear and surface topography of human dentin following simulated toothbrushing in vitro. 24 dentin specimens were prepared and randomly allocated to a liquid dentifrice (Garglin Gum-Guard), conventional dentifrice (333 Clinic Total Care), and control (distilled water) groups. Specimens were subjected to simulated toothbrushing of 50,000 repeated strokes under a 150 g-load. The dentin surface was profiled in each specimen using a profilometer before and after toothbrushing. The mean surface roughness (Ra) of the specimens was calculated and compared by one-way ANOVA and Tukey's post-hoc test (α = 0.05). The dentin surfaces were further examined by scanning electron microscopy (SEM). The Ra values were similar between the liquid dentifrice and control groups (P > 0.05), and was significantly higher in the conventional dentifrice group (P < 0.001). On SEM examination, patent dentin tubules were observed in the conventional dentifrice and liquid dentifrice groups, but were not observed in the control group.

  16. Determination of chlorobenzenes in textiles by pressurized hot water extraction followed by vortex-assisted liquid-liquid microextraction and gas chromatography-mass spectrometry.

    Science.gov (United States)

    Lu, Yang; Zhu, Yan

    2013-12-06

    A method for quantitative determination of chlorobenzenes in textiles is developed, using pressurized hot water extraction (PHWE), vortex-assisted liquid-liquid microextraction (VALLME) and gas chromatography-mass spectrometry (GC-MS). VALLME serves as a trapping step after PHWE. The extraction conditions are investigated, as well as the quantitative features such as linearity, limits of detection (LODs), limits of quantification (LOQs), repeatabilities and reproducibilities between days. LOQs of 0.018-0.032mg/kg were achieved. The present method provides good repeatabilities (RSDtextiles. Copyright © 2013 Elsevier B.V. All rights reserved.

  17. Liquid based formulations of bacteriophages for the management of waterborne bacterial pathogens in water microcosms.

    Science.gov (United States)

    Ahiwale, Sangeeta; Tagunde, Sujata; Khopkar, Sushama; Karni, Mrudula; Gajbhiye, Milind; Kapadnis, Balasaheb

    2013-11-01

    Water resources are contaminated by life-threatening multidrug resistant pathogenic bacteria. Unfortunately, these pathogenic bacteria do not respond to the traditional water purification methods. Therefore, there is a need of environmentally friendly strategies to overcome the problems associated with the antimicrobial resistant bacterial pathogens. In the present study, highly potent lytic phages against multidrug-resistant Salmonella enterica serovar Paratyphi B, Pseudomonas aeruginosa and Klebsiella pneumoniae were isolated from the Pavana river water. They belonged to the Podoviridae and Siphoviridae families. These phages were purified and enriched in the laboratory. Monovalent formulations of phiSPB, BVPaP-3 and KPP phages were prepared in three different liquids viz., phage broth, saline and distilled water. The phages were stable for almost 8-10 months in the phage broth at 4 degrees C. The stability of the phages in saline and distilled water was 5-6 months at 4 degrees C. All of the phages were stable only for 4-6 months in the phage broth at 30 degrees C. The monovalent phage formulation of psiSPB was applied at MOI Salmonella enterica serovar Paratyphi B in various water microcosms. The results indicated that there was almost 80 % reduction in the log phase cells of Salmonella serovar Paratyphi B in 24 h. In stationary phase cells, the reduction was comparatively less within same period. At the same time, there was concomitant increase in the phage population by 80% in all the microcosms indicating that psiSPB phage is highly potent in killing pathogen in water. Results strongly support that the formulation of psiSPB in the phage broth in monovalent form could be used as an effective biological disinfectant for preventing transmission of water-borne bacterial pathogens, including antimicrobial resistant ones.

  18. Infrared and Raman Spectroscopy of Liquid Water through "First-Principles" Many-Body Molecular Dynamics.

    Science.gov (United States)

    Medders, Gregory R; Paesani, Francesco

    2015-03-10

    Vibrational spectroscopy is a powerful technique to probe the structure and dynamics of water. However, deriving an unambiguous molecular-level interpretation of the experimental spectral features remains a challenge due to the complexity of the underlying hydrogen-bonding network. In this contribution, we present an integrated theoretical and computational framework (named many-body molecular dynamics or MB-MD) that, by systematically removing uncertainties associated with existing approaches, enables a rigorous modeling of vibrational spectra of water from quantum dynamical simulations. Specifically, we extend approaches used to model the many-body expansion of interaction energies to develop many-body representations of the dipole moment and polarizability of water. The combination of these "first-principles" representations with centroid molecular dynamics simulations enables the simulation of infrared and Raman spectra of liquid water under ambient conditions that, without relying on any ad hoc parameters, are in good agreement with the corresponding experimental results. Importantly, since the many-body energy, dipole, and polarizability surfaces employed in the simulations are derived independently from accurate fits to correlated electronic structure data, MB-MD allows for a systematic analysis of the calculated spectra in terms of both electronic and dynamical contributions. The present analysis suggests that, while MB-MD correctly reproduces both the shifts and the shapes of the main spectroscopic features, an improved description of quantum dynamical effects possibly combined with a dissociable water potential may be necessary for a quantitative representation of the OH stretch band.

  19. Study of a system for tritium analysis in water by electrolytic enrichment and liquid scintillation

    International Nuclear Information System (INIS)

    Pane, L.

    1979-01-01

    A system for the measurement of the low-level tritium concentrations in water samples has been experimentally studied. The enrichment of the samples is performed through electrolysis in twenty cells connected in series, and the counting is made in a liquid scintillation counter. Several parameters that could affect the accuracy of the results are analysed and the optimization of the system is discussed. For a sample volume reduction from 1000 to 15ml, the recovery of tritium, during electrolysis is of 63% and the enrichment factor is about 40. The lowest detection limit of the system is 1.0+-0.5 U.T. Its analytical capacity is of 30 samples a month. The results obtained in the determination of 3 H concentration in a series of samples from rain, surface and underground waters can be considered satisfactory. (Author) [pt

  20. Fate of major radionuclides in the liquid wastes released to coastal waters

    International Nuclear Information System (INIS)

    Bhat, I.S.; Verma, P.C.; Iyer, R.S.; Chandramouli, S.

    1980-01-01

    131 I, 134 Cs, 137 Cs and 60 Co have been reported as the major radionuclides in the low level liquid wastes released to coastal waters from atomic power stations. Silt absorption and desorption of the radionuclides were investigated. The exchangeability of the silt absorbed radionuclides and its dependence on particle size were also studied. More than 80% instantaneous absorpt;.on of 60 Co by suspended silt and less than 5% exchangeability of absorbed 60 Co were observed. Biological uptake of the radionuclides by the marine organisms present in sea waters was studied to evaluate radiation exposure pathways. A few benthic and crustacean organisms wnich are consumed by coastal population as fresh sea food, were observed to concentrate the radionuclides to a greater extent than other organisms. (H.K.)

  1. Trends in Particle-phase Liquid Water Measurements During the Southern Oxidant and Aerosol Study

    Science.gov (United States)

    Nguyen, T. V.; Petters, M. D.; Carlton, A. G.; Suda, S.

    2013-12-01

    Particle-phase liquid water (H2Optcl) contributes to total aerosol mass concentrations. Previous studies established links between inorganic species, particle hygroscopicity, ambient relative humidity, and condensed phase liquid water. These relationships are also included in thermodynamic modules of atmospheric chemistry models. Conversely, relationships between H2Optcl and organic species are poorly understood, and there are few field measurements linking the two. In this study, we present in situ measurements of H2Optcl using a newly developed technique - the semi-volatile differential mobility analysis (SVDMA). Measurements were conducted June 1 - July 15, 2013, during the Southern Oxidant and Aerosol Study (SOAS) in the southeast U.S., a biogenically dominated and photochemically active environment impacted by anthropogenic pollution and known to contain high concentrations of organic aerosol mass. The SVDMA measures volume distributions of ambient atmospheric aerosols in three states: unperturbed, dried, and dried then re-humidified. Unperturbed measurements characterize the aerosol distribution at ambient conditions. For dry spectra, the sample is routed through a cold trap (ΔT = -30K) upstream of the DMA inlet. The total volume of water and semi-volatile organic compounds (SVOCs) lost during drying is quantified by differencing dry and unperturbed volumes from the integrated size spectra, while SVOC volumes are quantified by re-humidifying the sample and referencing to the unperturbed state. Results indicate that liquid water is an important contributor to ambient aerosol volume in the southeast U.S. during the early morning period when the relative humidity differential is largest. Measured H2Optcl volumes can be characterized by hygroscopicity parameter κ ranging from 0.2 to 0.3, which is consistent with a mix of hygroscopic organic and inorganic compounds. Both H2Optcl and κ peak in the early morning when ambient relative humidity is decreasing

  2. The interplay between dynamic heterogeneities and structure of bulk liquid water: A molecular dynamics simulation study

    Energy Technology Data Exchange (ETDEWEB)

    Demontis, Pierfranco; Suffritti, Giuseppe B. [Dipartimento di Chimica e Farmacia, Università degli studi di Sassari, Sassari (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali (INSTM), Unità di ricerca di Sassari, Via Vienna, 2, I-07100 Sassari (Italy); Gulín-González, Jorge [Grupo de Matemática y Física Computacionales, Universidad de las Ciencias Informáticas (UCI), Carretera a San Antonio de los Baños, Km 21/2, La Lisa, La Habana (Cuba); Masia, Marco [Dipartimento di Chimica e Farmacia, Università degli studi di Sassari, Sassari (Italy); Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali (INSTM), Unità di ricerca di Sassari, Via Vienna, 2, I-07100 Sassari (Italy); Istituto Officina dei Materiali del CNR, UOS SLACS, Via Vienna 2, 07100 Sassari (Italy); Sant, Marco [Dipartimento di Chimica e Farmacia, Università degli studi di Sassari, Sassari (Italy)

    2015-06-28

    In order to study the interplay between dynamical heterogeneities and structural properties of bulk liquid water in the temperature range 130–350 K, thus including the supercooled regime, we use the explicit trend of the distribution functions of some molecular properties, namely, the rotational relaxation constants, the atomic mean-square displacements, the relaxation of the cross correlation functions between the linear and squared displacements of H and O atoms of each molecule, the tetrahedral order parameter q and, finally, the number of nearest neighbors (NNs) and of hydrogen bonds (HBs) per molecule. Two different potentials are considered: TIP4P-Ew and a model developed in this laboratory for the study of nanoconfined water. The results are similar for the dynamical properties, but are markedly different for the structural characteristics. In particular, for temperatures higher than that of the dynamic crossover between “fragile” (at higher temperatures) and “strong” (at lower temperatures) liquid behaviors detected around 207 K, the rotational relaxation of supercooled water appears to be remarkably homogeneous. However, the structural parameters (number of NNs and of HBs, as well as q) do not show homogeneous distributions, and these distributions are different for the two water models. Another dynamic crossover between “fragile” (at lower temperatures) and “strong” (at higher temperatures) liquid behaviors, corresponding to the one found experimentally at T{sup ∗} ∼ 315 ± 5 K, was spotted at T{sup ∗} ∼ 283 K and T{sup ∗} ∼ 276 K for the TIP4P-Ew and the model developed in this laboratory, respectively. It was detected from the trend of Arrhenius plots of dynamic quantities and from the onset of a further heterogeneity in the rotational relaxation. To our best knowledge, it is the first time that this dynamical crossover is detected in computer simulations of bulk water. On the basis of the simulation results, the possible

  3. A cobalt(II) bis(salicylate)-based ionic liquid that shows thermoresponsive and selective water coordination

    Energy Technology Data Exchange (ETDEWEB)

    Kohno, Y; Cowan, MG; Masuda, M; Bhowmick, I; Shores, MP; Gin, DL; Noble, RD

    2014-01-01

    A metal-containing ionic liquid (MCIL) has been prepared in which the [CoII(salicylate)(2)](2-) anion is able to selectively coordinate two water molecules with a visible colour change, even in the presence of alcohols. Upon moderate heating or placement in vacuo, the hydrated MCIL undergoes reversible thermochromism by releasing the bound water molecules.

  4. A cobalt(II) bis(salicylate)-based ionic liquid that shows thermoresponsive and selective water coordination.

    Science.gov (United States)

    Kohno, Yuki; Cowan, Matthew G; Masuda, Miyuki; Bhowmick, Indrani; Shores, Matthew P; Gin, Douglas L; Noble, Richard D

    2014-06-25

    A metal-containing ionic liquid (MCIL) has been prepared in which the [Co(II)(salicylate)2](2-) anion is able to selectively coordinate two water molecules with a visible colour change, even in the presence of alcohols. Upon moderate heating or placement in vacuo, the hydrated MCIL undergoes reversible thermochromism by releasing the bound water molecules.

  5. CGR MeV program for water and liquid sludges treatment with high-energy electron beams. Pt. 1

    International Nuclear Information System (INIS)

    Gallien, C.L.; Icre, P.; Levaillant, C.; Montiel, A.

    1976-01-01

    Research on the application of high-energy electron beams treatment to water and liquid sludges is described. Topics discussed include limitations of conventional methods of water treatment, dosimetry, biological assays with Pleurodeles waltlii, radioactivity measurement, chemical and bacteriological analysis. (author)

  6. Probing Properties of Glassy Water and Other Liquids with Site Selective Spectroscopies

    Energy Technology Data Exchange (ETDEWEB)

    Dang, Nhan Chuong [Iowa State Univ., Ames, IA (United States)

    2005-01-01

    The standard non-photochemical hole burning (NPHB) mechanism, which involves phonon-assisted tunneling in the electronically excited state, was originally proposed to explain the light-induced frequency change of chemically stable molecules in glassy solids at liquid helium temperatures by this research group more than two decades ago. The NPHB mechanism was then further elucidated and the concept of intrinsic to glass configurational relaxation processes as pre-mediating step to the hole burning process was introduced. The latter provided the theoretical basis for NPHB to evolve into a powerful tool probing the dynamics and nature of amorphous media, which aside from ''simple'' inorganic glasses may include also ''complex'' biological systems such as living cells and cancerous/normal tissues. Presented in this dissertation are the experimental and theoretical results of hole burning properties of aluminum phthalocyanine tetrasulphonate (APT) in several different matrices: (1) hyperquenched glassy water (HGW); (2) cubic ice (Ic); and (3) water confined into poly(2-hydroxyethylmethacrylate) (poly-HEMA). In addition, results of photochemical hole burning (PHB) studies obtained for phthalocyanine tetrasulphonate (PcT) in HGW and free base phthalocyanine (Pc) in ortho-dichlorobenzene (DCB) glass are reported. The goal of this dissertation was to provide further evidence supporting the NPHB mechanism and to provide more insight that leads to a better understanding of the kinetic events (dynamics) in glasses, and various dynamical processes of different fluorescent chromorphores in various amorphous solids and the liquid that exist above the glass transition temperature (Tg). The following issues are addressed in detail: (1) time evolution of hole being burned under different conditions and in different hole burning systems; (2) temperature dependent hole profile; and (3) the structure

  7. Exploration of the phase diagram of liquid water in the low-temperature metastable region using synthetic fluid inclusions

    DEFF Research Database (Denmark)

    Qiu, Chen; Krüger, Yves; Wilke, Max

    2016-01-01

    We present new experimental data of the low-temperature metastable region of liquid water derived from high-density synthetic fluid inclusions (996−916 kg/m3) in quartz. Microthermometric measurements include: i) Prograde (upon heating) and retrograde (upon cooling) liquid-vapour homogenisation. ...... a maximum of the bubble nucleation curve in the ϱ–T plane at around 40 °C. The new experimental data represent valuable benchmarks to evaluate and further improve theoretical models describing the p–V–T properties of metastable water in the low-temperature region......We present new experimental data of the low-temperature metastable region of liquid water derived from high-density synthetic fluid inclusions (996−916 kg/m3) in quartz. Microthermometric measurements include: i) Prograde (upon heating) and retrograde (upon cooling) liquid-vapour homogenisation. We...... used single ultrashort laser pulses to stimulate vapour bubble nucleation in initially monophase liquid inclusions. Water densities were calculated based on prograde homogenisation temperatures using the IAPWS-95 formulation. We found retrograde liquid-vapour homogenisation temperatures in excellent...

  8. Early Mars was wet but not warm: Erosion, fluvial features, liquid water habitats, and life below freezing

    Science.gov (United States)

    Mckay, C. P.; Davis, W. L.

    1993-01-01

    There is considerable evidence that Mars had liquid water early in its history and possibly at recurrent interval. It has generally been assumed that this implied that the climate was warmer as a result of a thicker CO2 atmosphere than at the present. However, recent models suggest that Mars may have had a thick atmosphere but may not have experienced mean annual temperatures above freezing. In this paper we report on models of liquid water formation and maintenance under temperatures well below freezing. Our studies are based on work in the north and south polar regions of Earth. Our results suggest that early Mars did have a thick atmosphere but precipitation and hence erosion was rare. Transient liquid water, formed under temperature extremes and maintained under thick ice covers, could account for the observed fluvial features. The main difference between the present climate and the early climate was that the total surface pressure was well above the triple point of water.

  9. Mercury Concentration Reduction In Waste Water By Using Liquid Surfactant Membrane Technique

    International Nuclear Information System (INIS)

    Prayitno; Sardjono, Joko

    2000-01-01

    The objective of this research is ti know effectiveness of liquid surfactant membrane in diminishing mercury found in waste water. This process can be regarded as transferring process of solved mercury from the external phase functioning as a moving phase to continue to the membrane internal one. The existence of the convection rotation results in the change of the surface pressure on the whole interface parts, so the solved mercury disperses on every interface part. Because of this rotation, the solved mercury will fulfil every space with particles from dispersion phase in accordance with its volume. Therefore, the change of the surface pressure on the whole interface parts can be kept stable to adsorb mercury. The mercury adsorbed in the internal phase moves to dispersed particles through molecule diffusion process. The liquid surfactant membrane technique in which the membrane phase is realized into emulsion contains os kerosene as solvent, sorbitan monoleat (span-80) 5 % (v/v) as surfactant, threbuthyl phosphate (TBP) 10 % (v/v) as extractant, and solved mercury as the internal phase. All of those things are mixed and stirred with 8000 rpm speed for 20 minutes. After the stability of emulsion is formed, the solved mercury is extracted by applying extraction process. The effective condition required to achieve mercury ion recovery utilizing this technique is obtained through extraction and re-extraction process. This process was conducted in 30 minutes with membrane and mercury in scale 1 : 1 on 100 ppm concentration. The results of the processes was 99,6 % efficiency. This high efficiency shows that the liquid surfactant membrane technique is very effective to reduce waste water contamined by mercury

  10. Dosimetric study of thermoluminescent detectors in clinical photon beams using liquid water and PMMA phantoms

    Energy Technology Data Exchange (ETDEWEB)

    Matsushima, Luciana C., E-mail: lmatsushima@ipen.br [Gerencia de Metrologia das Radiacoes (GMR) - Instituto de Pesquisas Energeticas e Nucleares (IPEN-CNEN/SP), Av. Prof. Lineu Prestes, 2242, Cidade Universitaria, CEP: 05508-000, Sao Paulo, SP (Brazil); Veneziani, Glauco R. [Gerencia de Metrologia das Radiacoes (GMR) - Instituto de Pesquisas Energeticas e Nucleares (IPEN-CNEN/SP), Av. Prof. Lineu Prestes, 2242, Cidade Universitaria, CEP: 05508-000, Sao Paulo, SP (Brazil); Sakuraba, Roberto K. [Gerencia de Metrologia das Radiacoes (GMR) - Instituto de Pesquisas Energeticas e Nucleares (IPEN-CNEN/SP), Av. Prof. Lineu Prestes, 2242, Cidade Universitaria, CEP: 05508-000, Sao Paulo, SP (Brazil); Sociedade Beneficente Israelita Brasileira - Hospital Albert Einstein (HAE), Avenida Albert Einstein, 665, Morumbi, CEP: 05652-000, Sao Paulo, SP (Brazil); Cruz, Jose C. da [Sociedade Beneficente Israelita Brasileira - Hospital Albert Einstein (HAE), Avenida Albert Einstein, 665, Morumbi, CEP: 05652-000, Sao Paulo, SP (Brazil)

    2012-07-15

    The purpose of this study was the dosimetric evaluation of thermoluminescent detectors of calcium sulphate doped with dysprosium (CaSO{sub 4}:Dy) produced by IPEN compared to the TL response of lithium fluoride doped with magnesium and titanium (LiF:Mg,Ti) dosimeters and microdosimeters produced by Harshaw Chemical Company to clinical photon beams dosimetry (6 and 15 MV) using liquid water and PMMA phantoms. - Highlights: Black-Right-Pointing-Pointer Dosimetric study of thermoluminescent detectors of CaSO{sub 4}:Dy, LiF:Mg,Ti and {mu}LiF:Mg,Ti. Black-Right-Pointing-Pointer Clinical (6 and 15 MV) photon beams dosimetry using liquid water and PMMA phantom. Black-Right-Pointing-Pointer Linear behavior to the dose range (0.1 to 5 Gy). Black-Right-Pointing-Pointer TL response reproducibility better than {+-}4.34%. Black-Right-Pointing-Pointer CaSO{sub 4}:Dy represent a cheaper alternative to the TLD-100.

  11. Anomalous partitioning of water in coexisting liquid phases of lipid multilayers near 100% relative humidity.

    Science.gov (United States)

    Ma, Yicong; Ghosh, Sajal K; Bera, Sambhunath; Jiang, Zhang; Schlepütz, Christian M; Karapetrova, Evguenia; Lurio, Laurence B; Sinha, Sunil K

    2016-01-14

    Ternary lipid mixtures incorporating cholesterol are well-known to phase separate into liquid-ordered (L(o)) and liquid-disordered (L(d)) phases. In multilayers of these systems, the laterally phase separated domains register in columnar structures with different bilayer periodicities, resulting in hydrophobic mismatch energies at the domain boundaries. In this paper, we demonstrate via synchrotron-based X-ray diffraction measurements that the system relieves the hydrophobic mismatch at the domain boundaries by absorbing larger amounts of inter-bilayer water into the L(d) phase with lower d-spacing as the relative humidity approaches 100%. The lamellar repeat distance of the L(d) phase swells by an extra 4 Å, well beyond the equilibrium spacing predicted by the inter-bilayer forces. This anomalous swelling is caused by the hydrophobic mismatch energy at the domain boundaries, which produces a surprisingly long-range effect. We also demonstrate that the d-spacings of the lipid multilayers at 100% relative humidity do not change when bulk water begins to condense on the sample.

  12. Enzymatic Saccharification and Ethanol Fermentation of Reed Pretreated with Liquid Hot Water

    Directory of Open Access Journals (Sweden)

    Jie Lu

    2012-01-01

    Full Text Available Reed is a widespread-growing, inexpensive, and readily available lignocellulosic material source in northeast China. The objective of this study is to evaluate the liquid hot water (LHW pretreatment efficiency of reed based on the enzymatic digestibility and ethanol fermentability of water-insoluble solids (WISs from reed after the LHW pretreatment. Several variables in the LHW pretreatment and enzymatic hydrolysis process were optimized. The conversion of glucan to glucose and glucose concentrations are considered as response variables in different conditions. The optimum conditions for the LHW pretreatment of reed area temperature of 180°C for 20min and a solid-to-liquid ratio of 1 : 10. These optimum conditions for the LHW pretreatment of reed resulted in a cellulose conversion rate of 82.59% in the subsequent enzymatic hydrolysis at 50°C for 72 h with a cellulase loading of 30 filter paper unit per gram of oven-dried WIS. Increasing the pretreatment temperature resulted in a higher enzymatic digestibility of the WIS from reed. Separate hydrolysis and fermentation of WIS showed that the conversion of glucan to ethanol reached 99.5% of the theoretical yield. The LHW pretreatment of reed is a suitable method to acquire a high recovery of fermentable sugars and high ethanol conversion yield.

  13. Electron microscopic observation of montmorillonite swelled by water with the aid of hydrophilic ionic liquid

    Energy Technology Data Exchange (ETDEWEB)

    Takahashi, Chisato [Advanced Ceramics Research Center, Nagoya Institute of Technology, Honmachi 3-101-1, Tajimi, Gifu 507-0033 (Japan); Department of Pharmaceutical Engineering, School of Pharmacy, Aichi Gakuin University, Kusumoto 1-100, Chikusa, Nagoya, Aichi 464-8650 (Japan); Shirai, Takashi [Advanced Ceramics Research Center, Nagoya Institute of Technology, Honmachi 3-101-1, Tajimi, Gifu 507-0033 (Japan); Fuji, Masayoshi, E-mail: fuji@nitech.ac.jp [Advanced Ceramics Research Center, Nagoya Institute of Technology, Honmachi 3-101-1, Tajimi, Gifu 507-0033 (Japan)

    2013-09-16

    The morphology and structure of hydrous montmorillonite in different swelling condition have been observed with the aid of hydrophilic ionic liquid (IL; 1-Butyl-3-methylimidazolium Tetrafluoroborate) using electron microscope. The observation mechanism of hydrous montmorillonite with layer structure using IL was revealed by swelling behavior as measured by X-ray diffraction (XRD) and transmission electron microscopy (TEM) with selected area electron diffraction pattern (SAED). The morphology of hydrous montmorillonite containing a large amount of water was also successfully observed by field emission electron microscope (FE-SEM). In addition, the inductively coupled plasma (ICP) and thermogravimetric – differential thermal analysis (TG-DTA) results showed the ion-exchange behavior of hydrous montmorillonite during the IL treatment. The technique allowed the exact morphology to be observed of hydrated materials with layer structure in civil engineering, cosmetics, medical and agricultural fields. - Highlights: • Observation of two different conditions of hydrated montmorillonite was investigated. • The swelling structure by water molecules was characterized by TEM. • The observation mechanism of hydrous montmorillonite was revealed. • Ionic liquid is useful for characterization of hydrated materials with layer structure.

  14. Hauled liquid waste as a pollutant of soils and waters in Poland

    Directory of Open Access Journals (Sweden)

    Karczmarczyk Agnieszka

    2016-06-01

    Full Text Available Hauled liquid waste as a pollutant of soils and waters in Poland. Improperly maintained holding tanks are often underestimated source of contamination of soil, groundwater and surface water. As a rule, wastewater stored in holding tanks, should be transported and treated in municipal wastewater treatment plants (WWTPs. There are 2,257,000 holding tanks in Poland, located mainly in rural areas. The article presents the results of analysis of wastewater management in 20 rural and urban-rural communes, which were chosen at random from the total number of 2,174 communes in Poland. The only criterion of commune selection was total or partial lack of sewerage system. Analysis of the collected data showed that on average only 27% of liquid waste from holding tanks ended at the WWTPs. The median is even lower and amounts to 17.5%. More than 4,000 Mg of P and 26,000 Mg of N is dispersed in the environment in uncontrolled manner. Those diffuse point sources of pollution may be one of the reasons in the difficulty of achieving of good ecological status of rivers and affect the quality of the Baltic Sea.

  15. Test of prototype liquid-water-content meter for aircraft use

    Science.gov (United States)

    Gerber, Hermann E.

    1993-01-01

    This report describes the effort undertaken to meet the objectives of National Science Foundation Grant ATM-9207345 titled 'Test of Prototype Liquid-Water-Content Meter for Aircraft Use.' Three activities were proposed for testing the new aircraft instrument, PVM-100A: (1) Calibrate the PVM-100A in a facility where the liquid-water-content (LWC) channel, and the integrated surface area channel (PSA) could be compared to standard means for LWC and PSA measurements. Scaling constant for the channels were to be determined in this facility. The fog/wind tunnel at ECN, Petten, The Netherlands was judged the most suitable facility for this effort. (2) Expose the PVM-100A to high wind speeds similar to those expected on research aircraft, and test the anti-icing heaters on the PVM-100A under typical icing conditions expected in atmospheric clouds. The high-speed icing tunnel at NRC, Ottawa, Canada was to be utilized. (3) Operate the PVM-100A on an aircraft during cloud penetrations to determine its stability and practicality for such measurements. The C-131A aircraft of the University of Washington was the aircraft of opportunity for these-tests, which were to be conducted during the 4-week Atlantic Stratocumulus Transition Experiment (ASTEX) in June of 1992.

  16. Gross alpha and gross beta determination in surface and groundwater water by liquid scintillation counting (LSC)

    Energy Technology Data Exchange (ETDEWEB)

    Faria, Ligia S.; Moreira, Rubens M., E-mail: ligsfaria@gmail.com, E-mail: rubens@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2013-07-01

    The present study has used 40 samples of groundwater and surface water collected at four different sites along the period of one year in Brumadinho and Nova Lima, two municipalities in the State of Minas Gerais, Brazil, as part of a more extensive study aiming at determination of the natural radioactivity in the water used for domestic use. These two sites are inside an Environmental Protection Area is located in a region of very intensive iron ore exploration. In addition of mineral resources, the region has a geological characteristic that includes quartzitic conglomerates associated with uranium. Radioactivity levels were determined via liquid scintillation counting (LSC), a fast and high counting efficiency method that can be advantageously employed to determine gross alpha and gross beta activity in liquid samples. Previously to gross alpha and gross beta counting the samples were acidified with concentrated HNO{sub 3} in the field. The technique involved a pre-concentration of the sample to obtain a low detection limit. Specific details of the employed methodology are commented. The results showed that concentrations of gross alpha natural activity and gross beta values ranged from less than the detection limit of the equipment (0.03 Bq.L{sup -1}) to 0.275 ± 0.05 Bq.L{sup -1} for gross alpha. As regards gross beta, all samples were below the limit of detection. (author)

  17. On the dissociative electron attachment as a potential source of molecular hydrogen in irradiated liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Cobut, V.; Jay-Gerin, J.-P.; Frongillo, Y. [Sherbrooke Univ., PQ (Canada). Faculte de Medecine; Patau, J.P. [Toulouse-3 Univ., 31 (France)

    1996-02-01

    In the radiolysis of liquid water, different mechanisms for the formation of molecular hydrogen (H{sub 2}) are involved at different times after the initial energy disposition. It has been suggested that the contributions of the e{sub aq}{sup -} + e{sub aq}{sup -}, H + e{sub aq}{sup -} and H + H reactions between hydrated electrons (e{sub aq}{sup -}) and hydrogen atoms in the spurs are not sufficient to account for all of the observed H{sub 2} yield (0.45 molecules/100 eV) on the microsecond time scale. Addressing the question of the origin of an unscavengeable H{sub 2} yield of 0.15 molecules/100 eV produced before spur expansion, we suggest that the dissociative capture of the so-called vibrationally-relaxing electrons by H{sub 2}O molecules is a possible pathway for the formation of part of the initial H{sub 2} yield. Comparison of recent dissociative-electron-attachment H{sup -}-anion yield-distribution measurements from amorphous H{sub 2}O films with the energy spectrum of vibrationally-relaxing electrons in irradiated liquid water, calculated by Monte Carlo simulations, plays in favor of this hypothesis. (author).

  18. RESEARCH ON TRANSFER OF LIQUID WATER ABSORPTION OF KNITTED STRUCTURES FOR SOCKS DESTINATION

    Directory of Open Access Journals (Sweden)

    VLAD Dorin

    2016-05-01

    Full Text Available For to adjust the heat, body removes heat. Depending on physical effort, it gives more or less moisture. Moisture removed from the body should be taken from the skin and directed outwards through clothing. This can be due to moisture absorption ability, and because of the capillary effect. This study is a part of a very extensive work on the influence of characteristics and raw materials, knitted structure and density on comfort properties of socks. If a high level of perspiration, moisture liquid, it is important that it be removed as quickly from skin and clothing led outside. From here can evaporate into the environment. This is achieved through the capillary effect of fabrics that may effectively transport moisture. Storage capacity and moisture transfer of a textile depends on the composition and structure. In laboratory conditions, methods for assessing the behavior of textiles against moisture is applied differentially depending on the state humidity: vapor or liquid. With this method of determining the capacity of absorbing water by capillary action, samples have dimensions of 200/200 mm and at one end is immersed in water. The samples knit were made in two versions of the fineness machine.

  19. Retrieval of Aerosol Liquid Water Path and Hygroscopic Growth from the AERONET database

    Science.gov (United States)

    Schuster, G. L.; Lin, B.; Dubovik, O.; Holben, B.; Sinyuk, A.

    2007-12-01

    Aerosol water uptake in the atmosphere alters aerosol size distributions, changes aerosol optical properties, and consequently impacts the aerosol radiative forcing. The parameterization of water uptake in aerosol transport models is empirical and unchecked, largely because of the lack of available measurements. We have developed a retrieval of the aerosol liquid water path (LWP) and hygroscopic growth using the AERONET database, and apply our results at over 200 AERONET locations. The real refractive index of prevalent atmospheric aerosols at the 500 nm wavelength ranges from 1.50 for sea salt to 1.56 for dust. Liquid water, on the other hand, has a real refractive index of 1.33 at 500 nm. We use this disparity in refractive indices to determine the equivalent water fractions for aerosol mixtures associated with the AERONET refractive index retrievals. Once the aerosol water fraction is known, we can also determine the hygroscopic growth factor, aerosol LWP, and the dry aerosol loading in the atmospheric column. Our aerosol LWP results are highly correlated with the following parameters: fine mode volume concentration, aerosol optical thickness (440 nm), aerosol water fraction, and coarse mode volume concentration (average correlation coefficients for all 200 sites ranges from 0.47 for the coarse mode concentration to 0.78 for the fine mode concentration). The regressions of these parameters have different slopes at each of the AERONET sites, which suggests a LWP sensitivity to aerosol composition. Aerosol liquid water path is not highly correlated with the mode radii or the fine mode volume fraction (average correlation coefficients for all sites range from 0.11 for the coarse mode median radius to 0.27 for the fine mode volume fraction). We compiled monthy-averaged statistics at over 200 AERONET locations based upon the daily-average AERONET retrievals; our results are consistent with regional and seasonal expectations. Aerosol water fractions range from a low

  20. Tile Drainage Management Influences on Surface-Water and Groundwater Quality following Liquid Manure Application.

    Science.gov (United States)

    Frey, Steven K; Topp, Ed; Ball, Bonnie R; Edwards, Mark; Gottschall, Natalie; Sunohara, Mark; Zoski, Erin; Lapen, David R

    2013-01-01

    This study investigated the potential for controlled tile drainage (CD) to reduce bacteria and nutrient loading to surface water and groundwater from fall-season liquid manure application (LMA) on four macroporous clay loam plots, of which two had CD and two had free-draining (FD) tiles. Rhodamine WT (RWT) was mixed into the manure and monitored in the tile water and groundwater following LMA. Tile water and groundwater quality were influenced by drainage management. Following LMA on the FD plots, RWT, nutrients, and bacteria moved rapidly via tiles to surface water; at the CD plots, tiles did not flow until the first post-LMA rainfall, so the immediate risk of LMA-induced contamination of surface water was abated. During the 36-d monitoring period, flow-weighted average specific conductance, redox potential, and turbidity, as well as total Kjeldahl N (TKN), total P (TP), NH-N, reactive P, and RWT concentrations, were higher in the CD tile effluent; however, because of lower tile discharge from the CD plots, there was no significant ( ≤ 0.05) difference in surface water nutrient and RWT loading between the CD and FD plots when all tiles were flowing. The TKN, TP, and RWT concentrations in groundwater also tended to be higher at the CD plots. Bacteria behaved differently than nutrients and RWT, with no significant difference in total coliform, , fecal coliform, fecal streptococcus, and concentrations between the CD and FD tile effluent; however, for all but , hourly loading was higher from the FD plots. Results indicate that CD has potential for mitigating bacteria movement to surface water. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  1. Computational studies of atmospherically-relevant chemical reactions in water clusters and on liquid water and ice surfaces.

    Science.gov (United States)

    Gerber, R Benny; Varner, Mychel E; Hammerich, Audrey D; Riikonen, Sampsa; Murdachaew, Garold; Shemesh, Dorit; Finlayson-Pitts, Barbara J

    2015-02-17

    CONSPECTUS: Reactions on water and ice surfaces and in other aqueous media are ubiquitous in the atmosphere, but the microscopic mechanisms of most of these processes are as yet unknown. This Account examines recent progress in atomistic simulations of such reactions and the insights provided into mechanisms and interpretation of experiments. Illustrative examples are discussed. The main computational approaches employed are classical trajectory simulations using interaction potentials derived from quantum chemical methods. This comprises both ab initio molecular dynamics (AIMD) and semiempirical molecular dynamics (SEMD), the latter referring to semiempirical quantum chemical methods. Presented examples are as follows: (i) Reaction of the (NO(+))(NO3(-)) ion pair with a water cluster to produce the atmospherically important HONO and HNO3. The simulations show that a cluster with four water molecules describes the reaction. This provides a hydrogen-bonding network supporting the transition state. The reaction is triggered by thermal structural fluctuations, and ultrafast changes in atomic partial charges play a key role. This is an example where a reaction in a small cluster can provide a model for a corresponding bulk process. The results support the proposed mechanism for production of HONO by hydrolysis of NO2 (N2O4). (ii) The reactions of gaseous HCl with N2O4 and N2O5 on liquid water surfaces. Ionization of HCl at the water/air interface is followed by nucleophilic attack of Cl(-) on N2O4 or N2O5. Both reactions proceed by an SN2 mechanism. The products are ClNO and ClNO2, precursors of atmospheric atomic chlorine. Because this mechanism cannot result from a cluster too small for HCl ionization, an extended water film model was simulated. The results explain ClNO formation experiments. Predicted ClNO2 formation is less efficient. (iii) Ionization of acids at ice surfaces. No ionization is found on ideal crystalline surfaces, but the process is efficient on

  2. Development of Nanostructured Water Treatment Membranes Based on Thermotropic Liquid Crystals: Molecular Design of Sub-Nanoporous Materials.

    Science.gov (United States)

    Sakamoto, Takeshi; Ogawa, Takafumi; Nada, Hiroki; Nakatsuji, Koji; Mitani, Masato; Soberats, Bartolome; Kawata, Ken; Yoshio, Masafumi; Tomioka, Hiroki; Sasaki, Takao; Kimura, Masahiro; Henmi, Masahiro; Kato, Takashi

    2018-01-01

    Supply of safe fresh water is currently one of the most important global issues. Membranes technologies are essential to treat water efficiently with low costs and energy consumption. Here, the development of self-organized nanostructured water treatment membranes based on ionic liquid crystals composed of ammonium, imidazolium, and pyridinium moieties is reported. Membranes with preserved 1D or 3D self-organized sub-nanopores are obtained by photopolymerization of ionic columnar or bicontinuous cubic liquid crystals. These membranes show salt rejection ability, ion selectivity, and excellent water permeability. The relationships between the structures and the transport properties of water molecules and ionic solutes in the sub-nanopores in the membranes are examined by molecular dynamics simulations. The results suggest that the volume of vacant space in the nanochannel greatly affects the water and ion permeability.

  3. Operation of a breadboard liquid-sorbent/membrane-contactor system for removing carbon dioxide and water vapor from air

    Science.gov (United States)

    Mccray, Scott B.; Ray, Rod; Newbold, David D.; Millard, Douglas L.; Friesen, Dwayne T.; Foerg, Sandra

    1992-01-01

    Processes to remove and recover carbon dioxide (CO2) and water vapor from air are essential for successful long-duration space missions. This paper presents results of a developmental program focused on the use of a liquid-sorbent/membrane-contactor (LSMC) system for removal of CO2 and water vapor from air. In this system, air from the spacecraft cabin atmosphere is circulated through one side of a hollow-fiber membrane contactor. On the other side of the membrane contactor is flowed a liquid sorbent, which absorbs the CO2 and water vapor from the feed air. The liquid sorbent is then heated to desorb the CO2 and water vapor. The CO2 is subsequently removed from the system as a concentrated gas stream, whereas the water vapor is condensed, producing a water stream. A breadboard system based on this technology was designed and constructed. Tests showed that the LSMC breadboard system can produce a CO2 stream and a liquid-water stream. Details are presented on the operation of the system, as well as the effects on performance of variations in feed conditions.

  4. Heterogeneous chemistry of NO{sub 3} in clouds and fogs

    Energy Technology Data Exchange (ETDEWEB)

    Rudich, Y.; Talukdar, R.K.; Fox, R. [NOAA, Aeronomy Lab., Boulder (United States)] [and others

    1996-10-01

    The heterogeneous reactions of the nitrate free radical (NO{sub 3}) an important nighttime oxidant in the lower troposphere, in clouds and fogs are unexplored. Therefore, the uptake coefficients ({gamma}) of NO{sub 3} onto pure water and other dilute solutions were measured. The product of Henry`s law constant, H, and diffusion coefficient D{sub {ell}}, for NO{sub 3} in water was calculated to be H{radical}D{sub {ell}} = (1.9{plus_minus}0.2)x10{sup -3} M atm{sup -1} cm s-{sup 1/2} and H , was determined to be 0.6{plus_minus}0.3 M atm{sup -1}. Uptake of NO{sub 3} on pure water is interpreted as due to reaction of NO{sub 3(aq)} with H{sub 2}O{sub ({ell})} to produce HNO{sub 3} and OH in the liquid phase. Details of these measurements and the implications of these findings to the chemistry of NO{sub 3} in the troposphere will discussed.

  5. Analysis and characterization of an optical fiber for Carrol-Water liquid pair

    International Nuclear Information System (INIS)

    Basurto-Pensado, M.A.; Romero, R.J.; Sanchez-Mondragon, J.J.; Dorantes-Romero, D.

    2011-01-01

    A system of energy recovery depends on the process operation conditions from which it receives the energy when a Carrol-Water pair is used. To improve the performance of the energy recovery system, the variables of temperature, pressure and concentration must be in balance. External sensors for temperature and pressure may be installed for all components. However, concentration is not determined online, and therefore an indirect method must be considered, such as optical transmittance correlation. Humidity contamination accounts for the hygroscopicity of Carrol water samples. The analysis of Carrol-Water optical characteristics is presented at multiple concentrations and temperatures, in which a transfer function involving absorbance and temperature is determined in order to define liquid pair concentration, as a function of actual temperature and signal intensity. This calculation provided the guideline to generate a control system that helps regulate thermal regimens. The characterization of this pair was made from temperature values ranging from 25 o C to 80 o C and mass concentration ranging from 51.79% to 66.2%. -- Highlights: → This paper shows a non invasive way for the Carrol-water concentration measurement. → The use of an optical technique using arbitrary units for a generalized transmittance method is proposed. → The in-line determination for concentration into an AHT (absorption heat transformer) allows to the operators lead to higher efficiencies. → Main advantage of the tested method is the simplification of the measured equipment required.

  6. Ionic liquids for the passive sampling of sulfonamides from water-applicability and selectivity study.

    Science.gov (United States)

    Męczykowska, Hanna; Kobylis, Paulina; Stepnowski, Piotr; Caban, Magda

    2017-06-01

    Ionic liquids (ILs) are new-generation, non-volatile solvents which are designable, and their structure may be specifically adjusted to the current application needs. Therefore, it is possible to create and apply ILs which efficiently and selectively extract various analytes from different matrices. It has already been examined that ILs may be applied as receiving phases in passive sampling for the long-term water monitoring of PAHs and pharmaceuticals in water. In this paper, the concept of passive sampling with ILs (PASSIL applied as receiving phases) was continued and developed using phosphonium-, imidazolium-, and morpholinium-cation-based ILs. The target group of analytes was pharmaceuticals which represent one of the most common categories of water contaminants. Fourteen-day-long extractions using various ILs were performed in stirred conditions at a constant temperature (20 °C). The best extraction efficiency was achieved for trihexyl(tetradecyl)phosphonium dicyanamide ([P666-14][N(CN) 2 ]). For this preliminary calibration, the sampling rates were calculated for each sulfonamide. Once again, selectivity was observed in passive sampling using [P666-14][N(CN) 2 ]. Therefore, PASSIL is seen as a very promising method for pharmaceutical monitoring in water.

  7. Combustion water purification techniques influence on OBT analysing using liquid scintillation counting method

    International Nuclear Information System (INIS)

    Varlam, C.; Vagner, I.; Faurescu, I.; Faurescu, D.

    2015-01-01

    In order to determine organically bound tritium (OBT) from environmental samples, these must be converted into water, measurable by liquid scintillation counting (LSC). For this purpose we conducted some experiments to determine OBT level of a grass sample collected from an uncontaminated area. The studied grass sample was combusted in a Parr bomb. However usual interfering phenomena were identified: color or chemical quench, chemiluminescence, overlap over tritium spectrum because of other radionuclides presence as impurities ( 14 C from organically compounds, 36 Cl as chloride and free chlorine, 40 K as potassium cations) and emulsion separation. So the purification of the combustion water before scintillation counting appeared to be essential. 5 purification methods were tested: distillation with chemical treatment (Na 2 O 2 and KMnO 4 ), lyophilization, chemical treatment (Na 2 O 2 and KMnO 4 ) followed by lyophilization, azeotropic distillation with toluene and treatment with a volcanic tuff followed by lyophilization. After the purification step each sample was measured and the OBT measured concentration, together with physico-chemical analysis of the water analyzed, revealed that the most efficient method applied for purification of the combustion water was the method using chemical treatment followed by lyophilization

  8. Combustion water purification techniques influence on OBT analysing using liquid scintillation counting method

    Energy Technology Data Exchange (ETDEWEB)

    Varlam, C.; Vagner, I.; Faurescu, I.; Faurescu, D. [National Institute for Cryogenics and Isotopic Technologies, Valcea (Romania)

    2015-03-15

    In order to determine organically bound tritium (OBT) from environmental samples, these must be converted into water, measurable by liquid scintillation counting (LSC). For this purpose we conducted some experiments to determine OBT level of a grass sample collected from an uncontaminated area. The studied grass sample was combusted in a Parr bomb. However usual interfering phenomena were identified: color or chemical quench, chemiluminescence, overlap over tritium spectrum because of other radionuclides presence as impurities ({sup 14}C from organically compounds, {sup 36}Cl as chloride and free chlorine, {sup 40}K as potassium cations) and emulsion separation. So the purification of the combustion water before scintillation counting appeared to be essential. 5 purification methods were tested: distillation with chemical treatment (Na{sub 2}O{sub 2} and KMnO{sub 4}), lyophilization, chemical treatment (Na{sub 2}O{sub 2} and KMnO{sub 4}) followed by lyophilization, azeotropic distillation with toluene and treatment with a volcanic tuff followed by lyophilization. After the purification step each sample was measured and the OBT measured concentration, together with physico-chemical analysis of the water analyzed, revealed that the most efficient method applied for purification of the combustion water was the method using chemical treatment followed by lyophilization.

  9. Water Pipeline Monitoring and Leak Detection using Flow Liquid Meter Sensor

    Science.gov (United States)

    Rahmat, R. F.; Satria, I. S.; Siregar, B.; Budiarto, R.

    2017-04-01

    Water distribution is generally installed through underground pipes. Monitoring the underground water pipelines is more difficult than monitoring the water pipelines located on the ground in open space. This situation will cause a permanent loss if there is a disturbance in the pipeline such as leakage. Leaks in pipes can be caused by several factors, such as the pipe’s age, improper installation, and natural disasters. Therefore, a solution is required to detect and to determine the location of the damage when there is a leak. The detection of the leak location will use fluid mechanics and kinematics physics based on harness water flow rate data obtained using flow liquid meter sensor and Arduino UNO as a microcontroller. The results show that the proposed method is able to work stably to determine the location of the leak which has a maximum distance of 2 metres, and it’s able to determine the leak location as close as possible with flow rate about 10 litters per minute.

  10. Dynamic crossover in deeply cooled water confined in MCM-41 at 4 kbar and its relation to the liquid-liquid transition hypothesis

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zhe; Le, Peisi; Ito, Kanae; Chen, Sow-Hsin, E-mail: sowhsin@mit.edu [Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States); Leão, Juscelino B. [National Institute of Standards and Technology Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899 (United States); Tyagi, Madhusudan [National Institute of Standards and Technology Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899 (United States); Department of Materials Science and Engineering, University of Maryland, College Park, Maryland 20742 (United States)

    2015-09-21

    With quasi-elastic neutron scattering, we study the single-particle dynamics of the water confined in a hydrophilic silica material, MCM-41, at 4 kbar. A dynamic crossover phenomenon is observed at 219 K. We compare this dynamic crossover with the one observed at ambient pressure and find that (a) above the crossover temperature, the temperature dependence of the characteristic relaxation time at ambient pressure exhibits a more evident super-Arrhenius behavior than that at 4 kbar. Especially, at temperatures below about 230 K, the relaxation time at 4 kbar is even smaller than that at ambient pressure. This feature is different from many other liquids. (b) Below the crossover temperature, the Arrhenius behavior found at ambient pressure has a larger activation energy compared to the one found at 4 kbar. We ascribe the former to the difference between the local structure of the low-density liquid (LDL) phase and that of the high-density liquid (HDL) phase, and the latter to the difference between the strength of the hydrogen bond of the LDL and that of the HDL. Therefore, we conclude that the phenomena observed in this paper are consistent with the LDL-to-HDL liquid-liquid transition hypothesis.

  11. Trace determination of volatile polycyclic aromatic hydrocarbons in natural waters by magnetic ionic liquid-based stir bar dispersive liquid microextraction.

    Science.gov (United States)

    Benedé, Juan L; Anderson, Jared L; Chisvert, Alberto

    2018-01-01

    In this work, a novel hybrid approach called stir bar dispersive liquid microextraction (SBDLME) that combines the advantages of stir bar sorptive extraction (SBSE) and dispersive liquid-liquid microextraction (DLLME) has been employed for the accurate and sensitive determination of ten polycyclic aromatic hydrocarbons (PAHs) in natural water samples. The extraction is carried out using a neodymium stir bar magnetically coated with a magnetic ionic liquid (MIL) as extraction device, in such a way that the MIL is dispersed into the solution at high stirring rates. Once the stirring is ceased, the MIL is magnetically retrieved onto the stir bar, and subsequently subjected to thermal desorption (TD) coupled to a gas chromatography-mass spectrometry (GC-MS) system. The main parameters involved in TD, as well as in the extraction step affecting the extraction efficiency (i.e., MIL amount, extraction time and ionic strength) were evaluated. Under the optimized conditions, the method was successfully validated showing good linearity, limits of detection and quantification in the low ng L -1 level, good intra- and inter-day repeatability (RSD < 13%) and good enrichment factors (18 - 717). This sensitive analytical method was applied to the determination of trace amounts of PAHs in three natural water samples (river, tap and rainwater) with satisfactory relative recovery values (84-115%), highlighting that the matrices under consideration do not affect the extraction process. Copyright © 2017 Elsevier B.V. All rights reserved.

  12. Use of water in aiding olefin/paraffin (liquid + liquid) extraction via complexation with a silver bis(trifluoromethylsulfonyl)imide salt

    International Nuclear Information System (INIS)

    Wang, Yu; Thompson, Jillian; Zhou, Jingjing; Goodrich, Peter; Atilhan, Mert; Pensado, Alfonso S.; Kirchner, Barbara; Rooney, David; Jacquemin, Johan; Khraisheh, Majeda

    2014-01-01

    Highlights: • Silver-based ILs used as olefin extracting agents for olefin/paraffin mixtures. • Each extraction process is based on the olefin complexation and solvation. • The presence of water influences positively each extraction process. • Each extraction process was evaluated by DFT calculations, NMR, IR and Raman. • LLE data were then correlated by using the UNIQUAC model. - Abstract: This paper describes the extraction of C 5 –C 8 linear α-olefins from olefin/paraffin mixtures of the same carbon number via a reversible complexation with a silver salt (silver bis(trifluoromethylsulfonyl)imide, Ag[Tf 2 N]) to form room temperature ionic liquids [Ag(olefin) x ][Tf 2 N]. From the experimental (liquid + liquid) equilibrium data for the olefin/paraffin mixtures and Ag[Tf 2 N], 1-pentene showed the best separation performance while C 7 and C 8 olefins could only be separated from the corresponding mixtures on addition of water which also improves the selectivity at lower carbon numbers like the C 5 and C 6 , for example. Using infrared and Raman spectroscopy of the complex and Ag[Tf 2 N] saturated by olefin, the mechanism of the extraction was found to be based on both chemical complexation and the physical solubility of the olefin in the ionic liquid ([Ag(olefin) x ][Tf 2 N]). These experiments further support the use of such extraction techniques for the separation of olefins from paraffins

  13. Development of an on-line mixed-mode gel liquid chromatography×reversed phase liquid chromatography method for separation of water extract from Flos Carthami.

    Science.gov (United States)

    Wang, Yu-Qing; Tang, Xu; Li, Jia-Fu; Wu, Yun-Long; Sun, Yu-Ying; Fang, Mei-Juan; Wu, Zhen; Wang, Xiu-Min; Qiu, Ying-Kun

    2017-10-13

    A novel on-line comprehensive two-dimensional liquid chromatography (2D-LC) method by coupling mixed-mode gel liquid chromatography (MMG-LC) with reversed phase liquid chromatography (RPLC) was developed. A mixture of 17 reference compounds was used to study the separation mechanism. A crude water extract of Flos Carthami was applied to evaluate the performance of the novel 2D-LC system. In the first dimension, the extract was eluted with a gradient of water/methanol over a cross-linked dextran gel Sephadex LH-20 column. Meanwhile, the advantages of size exclusion, reversed phase partition and adsorption separation mechanism were exploited before further on-line reversed phase purification on the second dimension. This novel on-line mixed-mode Sephadex LH-20×RPLC method provided higher peak resolution, sample processing ability (2.5mg) and better orthogonality (72.9%) versus RPLC×RPLC and hydrophilic interaction liquid chromatography (HILIC)×RPLC. To the best of our knowledge, this is the first report of a mixed-mode Sephadex LH-20×RPLC separation method with successful applications in on-line mode, which might be beneficial for harvesting targets from complicated medicinal plants. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Modeling the Liquid Water Transport in the Gas Diffusion Layer for Polymer Electrolyte Membrane Fuel Cells Using a Water Path Network

    Directory of Open Access Journals (Sweden)

    Dietmar Gerteisen

    2013-09-01

    Full Text Available In order to model the liquid water transport in the porous materials used in polymer electrolyte membrane (PEM fuel cells, the pore network models are often applied. The presented model is a novel approach to further develop these models towards a percolation model that is based on the fiber structure rather than the pore structure. The developed algorithm determines the stable liquid water paths in the gas diffusion layer (GDL structure and the transitions from the paths to the subsequent paths. The obtained water path network represents the basis for the calculation of the percolation process with low calculation efforts. A good agreement with experimental capillary pressure-saturation curves and synchrotron liquid water visualization data from other literature sources is found. The oxygen diffusivity for the GDL with liquid water saturation at breakthrough reveals that the porosity is not a crucial factor for the limiting current density. An algorithm for condensation is included into the model, which shows that condensing water is redirecting the water path in the GDL, leading to an improved oxygen diffusion by a decreased breakthrough pressure and changed saturation distribution at breakthrough.

  15. A New Dispersive Liquid-Liquid Microextraction Method for Preconcentration and Determination of Aluminum, Iron, Copper, and Lead in Real Water Samples by HPLC.

    Science.gov (United States)

    Alpdoğan, Güzin; Zor, Şule Dinç

    2017-09-01

    In this study, dispersive liquid-liquid microextraction coupled with HPLC with variable-wavelength detection was applied for the simultaneous determination of Al, Fe, Cu, and Pb in various water samples at trace levels. In the proposed method, all the system parameters in both the extraction and separation/determination steps, such as extraction and disperser solvent type and their volumes, complexing reagent concentration, salt addition, extraction and centrifugation times, and pH, were optimized to get not only high extraction efficiency but also lower LODs for the analytes. Hematoxylin was used as a complexing reagent, and carbon tetrachloride and methanol were chosen as the extraction and disperser solvents, respectively. Metal complexes were separated with a reversed-phase C18 column by isocratic elution, with methanol-tetrahydrofuran-water (20 + 12 + 68, v/v/v) as the mobile phase at a flow rate of 1.0 mL/min and detection at 575 nm. The accuracy of the method was checked by a Standard Reference Material of water (SRM 1643e), and the recovery values for the analytes were found in the range of 95.6-101.3%. Under the optimum conditions, the developed method was applied to tap water, bottled mineral water, lake water, and seawater for the accurate and sensitive determination of the analytes of interest.

  16. Spectral contaminant identifier for off-axis integrated cavity output spectroscopy measurements of liquid water isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Brian Leen, J.; Berman, Elena S. F.; Gupta, Manish [Los Gatos Research, 67 East Evelyn Avenue, Suite 3, Mountain View, California 94041-1518 (United States); Liebson, Lindsay [Department of Mechanical Engineering, Stanford University, Stanford, California 94305 (United States)

    2012-04-15

    Developments in cavity-enhanced absorption spectrometry have made it possible to measure water isotopes using faster, more cost-effective field-deployable instrumentation. Several groups have attempted to extend this technology to measure water extracted from plants and found that other extracted organics absorb light at frequencies similar to that absorbed by the water isotopomers, leading to {delta}{sup 2}H and {delta}{sup 18}O measurement errors ({Delta}{delta}{sup 2}H and {Delta}{delta}{sup 18}O). In this note, the off-axis integrated cavity output spectroscopy (ICOS) spectra of stable isotopes in liquid water is analyzed to determine the presence of interfering absorbers that lead to erroneous isotope measurements. The baseline offset of the spectra is used to calculate a broadband spectral metric, m{sub BB}, and the mean subtracted fit residuals in two regions of interest are used to determine a narrowband metric, m{sub NB}. These metrics are used to correct for {Delta}{delta}{sup 2}H and {Delta}{delta}{sup 18}O. The method was tested on 14 instruments and {Delta}{delta}{sup 18}O was found to scale linearly with contaminant concentration for both narrowband (e.g., methanol) and broadband (e.g., ethanol) absorbers, while {Delta}{delta}{sup 2}H scaled linearly with narrowband and as a polynomial with broadband absorbers. Additionally, the isotope errors scaled logarithmically with m{sub NB}. Using the isotope error versus m{sub NB} and m{sub BB} curves, {Delta}{delta}{sup 2}H and {Delta}{delta}{sup 18}O resulting from methanol contamination were corrected to a maximum mean absolute error of 0.93 per mille and 0.25 per mille respectively, while {Delta}{delta}{sup 2}H and {Delta}{delta}{sup 18}O from ethanol contamination were corrected to a maximum mean absolute error of 1.22 per mille and 0.22 per mille . Large variation between instruments indicates that the sensitivities must be calibrated for each individual isotope analyzer. These results suggest that the

  17. Optical Thickness and Effective Radius Retrievals of Liquid Water Clouds over Ice and Snow Surface

    Science.gov (United States)

    Platnick, S.; King, M. D.; Tsay, S.-C.; Arnold, G. T.; Gerber, H.; Hobbs, P. V.; Rangno, A.

    1999-01-01

    Cloud optical thickness and effective radius retrievals from solar reflectance measurements traditionally depend on a combination of spectral channels that are absorbing and non-absorbing for liquid water droplets. Reflectances in non-absorbing channels (e.g., 0.67, 0.86 micrometer bands) are largely dependent on cloud optical thickness, while longer wavelength absorbing channels (1.6, 2.1, and 3.7 micrometer window bands) provide cloud particle size information. Retrievals are complicated by the presence of an underlying ice/snow surface. At the shorter wavelengths, sea ice is both bright and highly variable, significantly increasing cloud retrieval uncertainty. However, reflectances at the longer wavelengths are relatively small and may be comparable to that of dark open water. Sea ice spectral albedos derived from Cloud Absorption Radiometer (CAR) measurements during April 1992 and June 1995 Arctic field deployments are used to illustrate these statements. A modification to the traditional retrieval technique is devised. The new algorithm uses a combination of absorbing spectral channels for which the snow/ice albedo is relatively small. Using this approach, preliminary retrievals have been made with the MODIS Airborne Simulator (MAS) imager flown aboard the NASA ER-2 during FIRE-ACE. Data from coordinated ER-2 and University of Washington CV-580 aircraft observations of liquid water stratus clouds on June 3 and June 6, 1998 have been examined. Size retrievals are compared with in situ cloud profile measurements of effective radius made with the CV-580 PMS FSSP probe, and optical thickness retrievals are compared with extinction profiles derived from the Gerber Scientific "g-meter" probe. MAS retrievals are shown to be in good agreement with the in situ measurements.

  18. Basic prerequisites and the practice of using deep water tables for burying liquid radioactive wastes

    International Nuclear Information System (INIS)

    Spitsyn, V.I.; Pimenov, M.K.; Balukova, V.D.; Leontichuk, A.S.; Kokorin, I.N.; Yudin, F.P.; Rakov, N.A.

    In the USSR, creating reservoirs for liquid radioactive wastes is one of the promising methods of safely disposing of them in deep water tables, in zones with a standing regime or a slow rate of subterranean water exchange. The results of investigations and the practice of burying (the wastes) indicate the reliability and effectiveness of such a method of final waste disposal when the basic requirements of environmental protection are observed. Geological formations and collector strata that guarantee the localization of the liquid radioactive wastes placed in them for many tens and even hundreds of thousands of years can be studied and chosen in different regions. The basic requirements and criteria to which the geological structures and collector strata must correspond for ensuring the safe burial of wastes have been formulated. Wastes are buried only after a comprehensive, scientifically based evaluation of the sanitary-radiation safety for this generation and future ones, taking into account the burial regime and the physico-chemical processes that accompany combining wastes with rocks and stratal waters, as well as the time of holding wastes to maximum permissible concentrations. Positive and negative factors that characterize the method are analyzed. Possible emergency situations with subterranean burial are evaluated. The composition and methods of the geological survey, hydrodynamic, geophysical, physico-chemical and sanitary-radiation investigations; methods of calculating and predicting the movement of wastes underground;methods of preparing wastes for burial and chemical methods of restoring the suitability of wells; design characteristics and conditions of preparing wells for use; methods of estimating heating and processes of radiolysis for a medium containing highly radioactive wastes; methods of operational and remote control of the burial process and the condition of the ambient medium, etc. are briefly examined

  19. In-situ ionic liquid dispersive liquid-liquid microextraction using a new anion-exchange reagent combined Fe3O4magnetic nanoparticles for determination of pyrethroid pesticides in water samples.

    Science.gov (United States)

    Fan, Chen; Liang, You; Dong, Hongqiang; Ding, Guanglong; Zhang, Wenbing; Tang, Gang; Yang, Jiale; Kong, Dandan; Wang, Deng; Cao, Yongsong

    2017-07-04

    In this work, in-situ ionic liquid dispersive liquid-liquid microextraction combined ultrasmall Fe 3 O 4 magnetic nanoparticles was developed as a kind of pretreatment method to detect pyrethroid pesticides in water samples. New anion-exchange reagents including Na[DDTC] and Na[N(CN) 2 ] were optimized for in-situ extraction pyrethroids, which showed enhanced microextraction performance. Pyrethroids were enriched by hydrophilic ionic liquid [P 4448 ][Br] (aqueous solution, 200 μL, 0.2 mmol mL -1 ) reaction in-situ with anion-exchange reagent Na[N(CN) 2 ] (aqueous solution, 300 μL, 0.2 mmol mL -1 ) forming hydrophobic ionic liquid as extraction agent in water sample (10 mL). Ultrasmall superparamagnetic iron oxide nanoparticles (30 mg) were used to collect the mixture of ionic liquid and pyrethroids followed by elution with acetonitrile. The extraction of ionic liquid strategies was unique and efficiently fulfilled with high enrichment factors (176-213) and good recoveries (80.20-117.31%). The method was successively applied to the determination of pyrethroid pesticides in different kinds of water samples with the limits of detection ranged from 0.16 to 0.21 μg L -1 . The proposed method is actually nanometer-level microextraction (average size 80 nm) with the advantages of simplicity, rapidity, and sensitivity. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. A study on the development of advanced models to predict the critical heat flux for water and liquid metals

    International Nuclear Information System (INIS)

    Lee, Yong Bum

    1994-02-01

    The critical heat flux (CHF) phenomenon in the two-phase convective flows has been an important issue in the fields of design and safety analysis of light water reactor (LWR) as well as sodium cooled liquid metal fast breeder reactor (LMFBR). Especially in the LWR application many physical aspects of the CHF phenomenon are understood and reliable correlations and mechanistic models to predict the CHF condition have been proposed. However, there are few correlations and models which are applicable to liquid metals. Compared with water, liquid metals show a divergent picture for boiling pattern. Therefore, the CHF conditions obtained from investigations with water cannot be applied to liquid metals. In this work a mechanistic model to predict the CHF of water and a correlation for liquid metals are developed. First, a mechanistic model to predict the CHF in flow boiling at low quality was developed based on the liquid sublayer dryout mechanism. In this approach the CHF is assumed to occur when a vapor blanket isolates the liquid sublayer from bulk liquid and then the liquid entering the sublayer falls short of balancing the rate of sublayer dryout by vaporization. Therefore, the vapor blanket velocity is the key parameter. In this work the vapor blanket velocity is theoretically determined based on mass, energy, and momentum balance and finally the mechanistic model to predict the CHF in flow boiling at low quality is developed. The accuracy of the present model is evaluated by comparing model predictions with the experimental data and tabular data of look-up tables. The predictions of the present model agree well with extensive CHF data. In the latter part a correlation to predict the CHF for liquid metals is developed based on the flow excursion mechanism. By using Baroczy two-phase frictional pressure drop correlation and Ledinegg instability criterion, the relationship between the CHF of liquid metals and the principal parameters is derived and finally the

  1. Detailed Information Security in Cloud Computing

    OpenAIRE

    Pavel Valerievich Ivonin

    2013-01-01

    The object of research in this article is technology of public clouds, structure and security system of clouds. Problems of information security in clouds are considered, elements of security system in public clouds are described.

  2. Structure and dynamics of POPC bilayers in water solutions of room temperature ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Benedetto, Antonio [School of Physics, University College Dublin, Dublin 4 (Ireland); Laboratory for Neutron Scattering and Imaging, Paul Scherrer Institut, 5232 Villigen (Switzerland); Bingham, Richard J. [York Centre for Complex Systems Analysis, University of York, York YO10 5GE (United Kingdom); Ballone, Pietro [Center for Life Nano Science @Sapienza, Istituto Italiano di Tecnologia (IIT), 00185 Roma (Italy); Department of Physics, Università di Roma “La Sapienza,” 00185 Roma (Italy)

    2015-03-28

    Molecular dynamics simulations in the NPT ensemble have been carried out to investigate the effect of two room temperature ionic liquids (RTILs), on stacks of phospholipid bilayers in water. We consider RTIL compounds consisting of chloride ([bmim][Cl]) and hexafluorophosphate ([bmim][PF{sub 6}]) salts of the 1-buthyl-3-methylimidazolium ([bmim]{sup +}) cation, while the phospholipid bilayer is made of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC). Our investigations focus on structural and dynamical properties of phospholipid and water molecules that could be probed by inelastic and quasi-elastic neutron scattering measurements. The results confirm the fast incorporation of [bmim]{sup +} into the lipid phase already observed in previous simulations, driven by the Coulomb attraction of the cation for the most electronegative oxygens in the POPC head group and by sizeable dispersion forces binding the neutral hydrocarbon tails of [bmim]{sup +} and of POPC. The [bmim]{sup +} absorption into the bilayer favours the penetration of water into POPC, causes a slight but systematic thinning of the bilayer, and further stabilises hydrogen bonds at the lipid/water interface that already in pure samples (no RTIL) display a lifetime much longer than in bulk water. On the other hand, the effect of RTILs on the diffusion constant of POPC (D{sub POPC}) does not reveal a clearly identifiable trend, since D{sub POPC} increases upon addition of [bmim][Cl] and decreases in the [bmim][PF{sub 6}] case. Moreover, because of screening, the electrostatic signature of each bilayer is only moderately affected by the addition of RTIL ions in solution. The analysis of long wavelength fluctuations of the bilayers shows that RTIL sorption causes a general decrease of the lipid/water interfacial tension and bending rigidity, pointing to the destabilizing effect of RTILs on lipid bilayers.

  3. Phase equilibria study of the binary systems (1-butyl-3-methylimidazolium tosylate ionic liquid + water, or organic solvent)

    International Nuclear Information System (INIS)

    Domanska, Urszula; Krolikowski, Marek

    2010-01-01

    (Solid + liquid) phase equilibria (SLE) and (liquid + liquid) phase equilibria (LLE) for the binary systems: ionic liquid (IL) 1-butyl-3-methylimidazolim tosylate (p-toluenesulfonate) {[BMIM][TOS] + water, an alcohol (ethanol, or 1-butanol, or 1-hexanol, or 1-octanol, or 1-decanol), or n-hexane, or an aromatic hydrocarbons (benzene, or toluene, or ethylbenzene, or propylbenzene, or thiophene)} have been determined at ambient pressure. A dynamic method was used over a broad range of mole fractions and temperatures from (230 to 340) K. For the binary systems containing water, or an alcohol, simple eutectic diagrams were observed with complete miscibility in the liquid phase. As usual, with increasing chain length of the alcohol the solubility decreases. In the case of mixtures {IL + n-hexane, or benzene, or alkylbenzene, or thiophene} the eutectic systems with mutual immiscibility in the liquid phase with an upper critical solution temperature (UCST) were detected. The basic thermal properties of the pure IL, i.e. melting and glass-transition temperatures, as well as the enthalpy of fusion have been measured using a differential scanning microcalorimetry technique (DSC). Density at high temperatures was determined and extrapolated to 298.15 K. Well-known UNIQUAC, Wilson and NRTL equations have been used to correlate experimental SLE data sets for alcohols and water. For the systems containing immiscibility gaps {IL + n-hexane, or benzene, or alkylbenzene, or thiophene}, parameters of the LLE correlation equation have been derived using only the NRTL equation.

  4. Microwave measurements of temperature profiles, integrated water vapour, and liquid water path at Thule Air Base, Greenland.

    Science.gov (United States)

    Pace, Giandomenico; Di Iorio, Tatiana; di Sarra, Alcide; Iaccarino, Antonio; Meloni, Daniela; Mevi, Gabriele; Muscari, Giovanni; Cacciani, Marco

    2017-04-01

    A RPG Humidity And Temperature PROfiler (HATPRO-G2 ) radiometer was installed at Thule Air Base (76.5° N, 68.8° W), Greenland, in June 2016 in the framework of the Study of the water VApour in the polar AtmosPhere (SVAAP) project. The Danish Meteorological Institute started measurements of atmospheric properties at Thule Air Base in early '90s. The Thule High Arctic Atmospheric Observatory (THAAO) has grown in size and observing capabilities during the last three decades through the international effort of United States (NCAR and University of Alaska Fairbanks) and Italian (ENEA, INGV, University of Roma and Firenze) institutions (http://www.thuleatmos-it.it). Within this context, the intensive field campaign of the SVAAP project was aimed at the investigation of the surface radiation budget and took place from 5 to 28 July, 2016. After the summer campaign the HATPRO has continued to operate in order to monitor the annual variability of the temperature profile and integrated water vapour as well as the presence and characteristics of liquid clouds in the Artic environment. The combined use of the HATPRO together with other automatic instruments, such as a new microwave spectrometer (the water Vapour Emission Spectrometer for Polar Atmosphere VESPA-22), upward- and downward-looking pyranometers and pyrgeometers, a zenith-looking pyrometer operating in the 9.6-11.5 µm spectral range, an all sky camera, and a meteorological station, allows to investigate the clouds' physical and optical properties, as well as their impact on the surface radiation budget. This study will present and discuss the first few months of HATPRO observations; the effectiveness of the statistical retrieval used to derive the physical parameters from the HATPRO brightness temperatures will also be investigated through the comparison of the temperature and humidity profiles, and integrated water vapour, with data from radiosondes launched during the summer campaign and in winter time.

  5. Satellite retrieval of the liquid water fraction in tropical clouds between −20 and −38 °C

    Directory of Open Access Journals (Sweden)

    D. L. Mitchell

    2012-07-01

    Full Text Available This study describes a satellite remote sensing method for directly retrieving the liquid water fraction in mixed phase clouds, and appears unique in this respect. The method uses MODIS split-window channels for retrieving the liquid fraction from cold clouds where the liquid water fraction is less than 50% of the total condensate. This makes use of the observation that clouds only containing ice exhibit effective 12-to-11 μm absorption optical thickness ratios (βeff that are quasi-constant with retrieved cloud temperature T. This observation was made possible by using two CO2 channels to retrieve T and then using the 12 and 11 μm channels to retrieve emissivities and βeff. Thus for T < −40 °C, βeff is constant, but for T > −40 °C, βeff slowly increases due to the presence of liquid water, revealing mean liquid fractions of ~ 10% around −22 °C from tropical clouds identified as cirrus by the cloud mask. However, the uncertainties for these retrievals are large, and extensive in situ measurements are needed to refine and validate these retrievals. Such liquid levels are shown to reduce the cloud effective diameter De such that cloud optical thickness will increase by more than 50% for a given water path, relative to De corresponding to pure ice clouds. Such retrieval information is needed for validation of the cloud microphysics in climate models. Since low levels of liquid water can dominate cloud optical properties, tropical clouds between −25 and −20 °C may be susceptible to the first aerosol indirect effect.

  6. Filling environmental data gaps with QSPR for ionic liquids: Modeling n-octanol/water coefficient.

    Science.gov (United States)

    Rybinska, Anna; Sosnowska, Anita; Grzonkowska, Monika; Barycki, Maciej; Puzyn, Tomasz

    2016-02-13

    Ionic liquids (ILs) form a wide group of compounds characterized by specific properties that allow using ILs in different fields of science and industry. Regarding that the growing production and use of ionic liquids increase probability of their emission to the environment, it is important to estimate the ability of these compounds to spread in the environment. One of the most important parameters that allow evaluating environmental mobility of compound is n-octanol/water partition coefficient (KOW). Experimental measuring of the KOW values for a large number of compounds could be time consuming and costly. Instead, computational predictions are nowadays being used more often. The paper presents new Quantitative Structure-Property Relationship (QSPR) model that allows predicting the logarithmic values of KOW for 335 ILs, for which the experimentally measured values had been unavailable. We also estimated bioaccumulation potential and point out which group of ILs could have negative impact on environment. Copyright © 2015 Elsevier B.V. All rights reserved.

  7. Flow and heat transfer in water based liquid film fluids dispensed with graphene nanoparticles

    Science.gov (United States)

    Zuhra, Samina; Khan, Noor Saeed; Khan, Muhammad Altaf; Islam, Saeed; Khan, Waris; Bonyah, Ebenezer

    2018-03-01

    The unsteady flow and heat transfer characteristics of electrically conducting water based thin liquid film non-Newtonian (Casson and Williamson) nanofluids dispensed with graphene nanoparticles past a stretching sheet are considered in the presence of transverse magnetic field and non-uniform heat source/sink. Embedding the graphene nanoparticles effectively amplifies the thermal conductivity of Casson and Williamson nanofluids. Ordinary differential equations together with the boundary conditions are obtained through similarity variables from the governing equations of the problem, which are solved by the HAM (Homotopy Analysis Method). The solution is expressed through graphs and illustrated which show the influences of all the parameters. The convergence of the HAM solution for the linear operators is obtained. Favorable comparison with previously published research paper is performed to show the correlation for the present work. Skin friction coefficient and Nusselt number are presented through Tables and graphs which show the validation for the achieved results demonstrating that the thin liquid films results from this study are in close agreement with the results reported in the literature. Results achieved by HAM and residual errors are evaluated numerically, given in Tables and also depicted graphically which show the accuracy of the present work.

  8. Effects of water chemistry on flow accelerated corrosion and liquid droplet impingement

    International Nuclear Information System (INIS)

    Uchida, Shunsuke; Naitoh, Masanori; Okada, Hidetoshi; Uehara, Yasushi; Koshizuka, Seiichi; Lister, Derek H.

    2009-01-01

    Overlapping effects of flow dynamics and corrosion are important issues to determine reliability and lifetime of major structures and components in light water reactor plants. Flow accelerated corrosion (FAC) and liquid droplet impingement (LDI) are typical phenomena due to both interactions. In order to evaluation local wall thinning due to FAC and LDI, 6 step evaluation procedures have been proposed. (1) Flow pattern along the flow path was obtained with 1D computational flow dynamics (CFD) codes, (2) Corrosive conditions, e.g., oxygen concentration along the flow path were calculated with a hydrazine oxygen reaction code for FAC evaluation, while flow pattern of liquid droplets in high velocity steam and possibility of their collision to pipe inner surface were evaluated for LDI evaluation. (3) Mass transfer coefficient at the structure surface was calculated with 3D CFD codes for FAC evaluation, while frequency of oxide film rupture due to droplet collision was calculated for LDI evaluation. (4) High risk zones for FAC/LDI occurrence were evaluated by coupling major parameters, and then, (5) Wall thinning rates were calculated with the coupled model of static electrochemical analysis and dynamic double oxide layer analysis at the identified high FAC/LDI risk zone. (author)

  9. New determination method of radon-220 in water by toluene extraction and liquid scintillation counter

    International Nuclear Information System (INIS)

    Horiuchi, Kimiko; Murakami, Yukio

    1979-01-01

    220 Rn in mineral springs is easily extracted into toluene solution (containing a definite amount of liquid scientillator), which is carefuly transferred into counting vial. The activity in the solution is measured by integral counting technique with a liquid scintillation counter. 220 Rn, being extracted, rapidly disappears but 212 Pb (half-life 10.64 h) and its descendants form a radioactive equilibrium in toluene solution around 3.7 h after the extraction. The establishment of radioactive equilibrium is proved by α and β rays energy spectrum and also by the formation of growth decay curve. The shape of this curve entirely coincides with decay curve constructed by application of the Bateman equations for 212 Pb and its descendants. It was proved that integral counting technique could practically give hundred percent counting efficiency for 1α and 2β emitters in radioactive equilibrium. A calculating formula for 220 Rn contents in water is proposed based upon these facts, together with necessary correction terms such as extractability, decay rate during measurement and so on. The detection limits of this method is found as (6.8 +- 0.9) x 10 -10 Ci (standard deviation incounting) under the conditions of 5 cpm (one tenth of background counting rate) and total counting time of 400 min. Some practical examples of determination of 220 Rn in mineral springs are shown together with 222 Rn contents to prove the availability and feasibility of this method. (author)

  10. Catalysis of deuterium transfer between liquid chloroform and water by anion-exchange resins

    International Nuclear Information System (INIS)

    Symons, E.A.; Bonnett, J.D.

    1985-01-01

    Anion-exchange resins in the hydroxide form have been successfully utilized for catalysis of deuterium transfer between water and liquid chloroform under stirred three-phase slurry conditions. In-solution rate constants for CDCl 3 /H 2 O exchange obtained at 15-35 0 C with liquid chloroform and 0.10 mol/liter NaOH solution under stirred conditions are in good agreement with literature data measured in the absence of bulk chloroform. At 25 0 C the resins tested, Rexyn 201(OH) and Ionac ASB-1P(OH), are ∼25x more effective per mole of - OH present than NaOH when they are used as whole beads. A further improvement is observed if the beads are crushed, but the latter state would be less suitable for commercial-scale application. The solubility of chloroform in the aqueous phase under isotope-exchange conditions was required to calculate the in-solution rate constants for exchange. A method was developed to obtain chloroform solubilities in 0.10 mol/liter NaOH solution and aqueous resin slurries; equilibrated solution samples were treated with 1 mol/liter NaOH to hydrolyze the dissolved CHCl 3 to chloride ion, which was then analyzed by specific ion electrode. 25 references, 2 figures, 1 table

  11. Microalgae pretreatment with liquid hot water to enhance enzymatic hydrolysis efficiency.

    Science.gov (United States)

    Yuan, Tao; Li, Xiekun; Xiao, Shiyuan; Guo, Ying; Zhou, Weizheng; Xu, Jingliang; Yuan, Zhenhong

    2016-11-01

    Nowadays, microalgae are being considered as promising raw material for bioethanol production. In this work, three process variables during liquid hot water (LHW) pretreatment prior to enzymatic hydrolysis by response surface methodology on Scenedesmus sp. WZKMT were investigated to enhance glucose recovery. Results indicated that the order of significance for three parameters was temperature>solid-to-liquid ratio>time. The optimal condition was 1:13 (w/v), 147°C and 40min. The concentration and recovery of glucose under this condition were 14.223g·L(-1) and 89.32%, respectively, which were up to 5-fold higher than the samples without LHW pretreatment. In addition, the surface morphologies of microalgae cells before and after LHW pretreatment were also verified using scanning electron microscopy (SEM). LHW pretreatment can greatly enhance the enzymatic efficiency, and can be regarded as an ideal pretreatment method for glucose recovery from microalgae. Copyright © 2016 Elsevier Ltd. All rights reserved.

  12. PHASE EQUILIBRIA FOR BINARY SYSTEMS CONTAINING IONIC LIQUID WITH WATER OR HYDROCARBONS

    Directory of Open Access Journals (Sweden)

    Dheiver Santos

    2015-12-01

    Full Text Available Abstract In this work, the mutual solubilities of sets of ionic liquids ([CnMIM] [TF2N] (n = 4, 8, 12, [C4PY] [TF2N], [C8MIM] [OTF] and organic compounds (heptane, o-xylene, toluene, or water are investigated. The experimental data measured for these systems were used to adjust the binary interaction parameters between their components for the Non-Random Two Liquid (NRTL model. The results showed that the solubility increased with temperature, with high hygroscopicity (10-1 in terms of mole fraction of the ILs, low interactions with aliphatic hydrocarbons, high interactions with aromatic hydrocarbons and the presence of a lower critical solution temperature (LCST. In addition, this study is the first to show that [C12MIM] [TF2N] is completely soluble in toluene and ortho-xylene between 273.15 and 373.15 K at 1 bar. The average deviations related to the mole fraction between the experimental and calculated values by the NRTL were less than 2.4%.

  13. Water Flow Testing and Unsteady Pressure Analysis of a Two-Bladed Liquid Oxidizer Pump Inducer

    Science.gov (United States)

    Schwarz, Jordan B.; Mulder, Andrew; Zoladz, Thomas

    2011-01-01

    The unsteady fluid dynamic performance of a cavitating two-bladed oxidizer turbopump inducer was characterized through sub-scale water flow testing. While testing a novel inlet duct design that included a cavitation suppression groove, unusual high-frequency pressure oscillations were observed. With potential implications for inducer blade loads, these high-frequency components were analyzed extensively in order to understand their origins and impacts to blade loading. Water flow testing provides a technique to determine pump performance without the costs and hazards associated with handling cryogenic propellants. Water has a similar density and Reynolds number to liquid oxygen. In a 70%-scale water flow test, the inducer-only pump performance was evaluated. Over a range of flow rates, the pump inlet pressure was gradually reduced, causing the flow to cavitate near the pump inducer. A nominal, smooth inducer inlet was tested, followed by an inlet duct with a circumferential groove designed to suppress cavitation. A subsequent 52%-scale water flow test in another facility evaluated the combined inducer-impeller pump performance. With the nominal inlet design, the inducer showed traditional cavitation and surge characteristics. Significant bearing loads were created by large side loads on the inducer during synchronous cavitation. The grooved inlet successfully mitigated these loads by greatly reducing synchronous cavitation, however high-frequency pressure oscillations were observed over a range of frequencies. Analytical signal processing techniques showed these oscillations to be created by a rotating, multi-celled train of pressure pulses, and subsequent CFD analysis suggested that such pulses could be created by the interaction of rotating inducer blades with fluid trapped in a cavitation suppression groove. Despite their relatively low amplitude, these high-frequency pressure oscillations posed a design concern due to their sensitivity to flow conditions and

  14. The measurement of Rn-222 in drinking water by low-level liquid scintillation counting

    International Nuclear Information System (INIS)

    Barnett, J.M.; McKlveen, J.W.

    1991-01-01

    Radon-222 has consistently been found in well water. The research objectives are to establish a method to collect well water and to measure the Rn in ground water using liquid scintillation (LS) counting. Water is collected at the well head while the well is pumping. The water is adjusted to a slow, non-aerated, steady flow through a clear tube, and a 437 mL (16 oz) glass bottle is filled. The sample is tightly capped after a high meniscus has developed. In the laboratory, standard 22 mL LS glass vials are filled with 10 mL of a toluene based mineral oil LS cocktail. Then, two 5 mL sample aliquots are pipetted into the vial. Vials are capped tightly, shaken vigorously, and placed in the LS counter. Secular equilibrium is established in approximately 3.5 hours, after which samples are counted for 100 minutes each. Quality assurance and control is performed weekly on the LS counter's electronics, spectral window, counting efficiency, and background. The counting efficiency ranges between 315-345 percent depending on the chosen spectral window. The average background is about 6 cpm. A total of 28 wells were tested for Rn in the Carefree-Cave Creek, Arizona, USA area, and 12 wells were selected, each over 50 Bq/L (1,350 pCi/L), for an extended 6 month period. The area's average Rn concentration was found to be 46.5 Bq/L (1,255 pCi/L); it is a geometric mean. The associated estimated lung dose is 1.13 mSv/a

  15. Determination of Trichloroethylene in Water by Liquid–Liquid Microextraction Assisted Solid Phase Microextraction

    Directory of Open Access Journals (Sweden)

    Mengliang Zhang

    2015-02-01

    Full Text Available A method for the determination of trichloroethylene (TCE in water using portable gas chromatography/mass spectrometry (GC/MS was developed. A novel sample preparation method, liquid–liquid microextraction assisted solid phase microextraction (LLME–SPME, is introduced. In this method, 20 µL of hexane was added to 10 mL of TCE contaminated aqueous samples to assist headspace SPME. The extraction efficiency of SPME was significantly improved with the addition of minute amounts of organic solvents (i.e., 20 µL hexane. The absolute recoveries of TCE at different concentrations were increased from 11%–17% for the samples extracted by SPME to 29%–41% for the samples extracted by LLME–SPME. The method was demonstrated to be linear from 10 to 1000 ng mL−1 for TCE in water. The improvements on extraction efficiencies were also observed for toluene and 1, 2, 4-trichlorobenzene in water by using LLME–SPME method. The LLME–SPME method was optimized by using response surface modeling (RSM.

  16. Assessment of three turbulence model performances in predicting water jet flow plunging into a liquid pool

    Directory of Open Access Journals (Sweden)

    Zidouni Kendil Faiza

    2010-01-01

    Full Text Available The main purpose of the current study is to numerically investigate, through computational fluid dynamics modeling, a water jet injected vertically downward through a straight circular pipe into a water bath. The study also aims to obtain a better understanding of jet behavior, air entrainment and the dispersion of bubbles in the developing flow region. For these purposes, three dimensional air and water flows were modeled using the volume of fluid technique. The equations in question were formulated using the density and viscosity of a 'gas-liquid mixture', described in terms of the phase volume fraction. Three turbulence models with a high Reynolds number have been considered i. e. the standard k-e model, realizable k-e model, and Reynolds stress model. The predicted flow patterns for the realizable k-e model match well with experimental measurements found in available literature. Nevertheless, some discrepancies regarding velocity relaxation and turbulent momentum distribution in the pool are still observed for both the standard k-e and the Reynolds stress model.

  17. Effects of tetrachloroethene on the measurement of radon in water with liquid scintillation counting method.

    Science.gov (United States)

    Chen, Yao-Tsung; Lu, Chih-Jen

    2014-01-01

    This study investigated the effects of tetrachloroethene (PCE) on radon measurements that employed the liquid scintillation counting (LSC) method referring to 7500-Rn B of Standard Methods for the Examination of Water and Wastewater. Laboratory-produced radon-enriched water was used to compare the counting rates of the radon water with and without PCE addition, and groundwater samples from a site contaminated by chlorinated solvents were used to investigate the application of the laboratory experiments. The results showed that the major factor reducing counting efficiency was resulted from the interaction between PCE and a cocktail through the quench effect. The counting rate showed an exponentially decreasing trend when PCE addition was increased. The results indicated that a small addition of PCE reduced the counting rate considerably. An alternative energy channel 500-1000 to the optimal channel was suggested to attenuate the quench effect on radon measurement. The quench effect was also observed on samples from a site contaminated by chlorinated solvents. The concepts and procedures presented in this study are a reference for future research on the topic of chlorinated solvents or other quench chemicals involving in radon measurement. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

  18. The measurement of 222Rn in drinking water by low-level liquid scintillation counting

    International Nuclear Information System (INIS)

    Barnett, J.M.; McKlveen, J.W.

    1992-01-01

    Radon-222 (Rn) has universally been found in well water. Non-stagnant ground water is collected at the well head while the well is pumping. The water is adjusted to a slow, non-aerated, steady flow through a clear tube, and a 500 ml glass bottle is filled. The sample is tightly capped after a high meniscus has developed. In the laboratory, standard 22 ml glass vials are filled with 10 ml of a toluene based mineral oil LS cocktail. Then, two 5 ml sample aliquots are pipetted into the vial. Vials are capped tightly, shaken vigorously, and placed in the liquid scintillation (LS) counter. Secular equilibrium is established in approximately 4 hours, after which samples are counted for 100 minutes each. The counting efficiency for Rn and progeny ranges between 315 to 345 percent depending on the chosen spectral window. The average background is about 6 cpm. A total of 28 wells were tested for Rn in the Carefree-Cave Creek, Arizone, USA area. The area's geometric average Rn concentration was found to be 46.5 Bq*1 -1 . The associated estimated lung dose is 0.51 mSv*y -1 . (author) 8 refs.; 1 fig.; 1 tab

  19. Experimental Investigation of Gas Hydrate Production at Injection of Liquid Nitrogen into Water with Bubbles of Freon 134A

    Directory of Open Access Journals (Sweden)

    Meleshkin Anton V.

    2016-01-01

    Full Text Available The hydrodynamic processes during the injection of the cryogenic liquid into the volume of water with bubbles of gas freon 134a are studding experimentally. A processes during the explosive boiling of liquid nitrogen in the volume of water are registered. Video recording of identified gas hydrate flakes formed during this process is carried out by high speed camera. These results may be useful for the study of the new method of producing gas hydrates, based on the shock-wave method.

  20. Vibrating-Wire, Supercooled Liquid Water Content Sensor Calibration and Characterization Progress

    Science.gov (United States)

    King, Michael C.; Bognar, John A.; Guest, Daniel; Bunt, Fred

    2016-01-01

    NASA conducted a winter 2015 field campaign using weather balloons at the NASA Glenn Research Center to generate a validation database for the NASA Icing Remote Sensing System. The weather balloons carried a specialized, disposable, vibrating-wire sensor to determine supercooled liquid water content aloft. Significant progress has been made to calibrate and characterize these sensors. Calibration testing of the vibrating-wire sensors was carried out in a specially developed, low-speed, icing wind tunnel, and the results were analyzed. The sensor ice accretion behavior was also documented and analyzed. Finally, post-campaign evaluation of the balloon soundings revealed a gradual drift in the sensor data with increasing altitude. This behavior was analyzed and a method to correct for the drift in the data was developed.

  1. Mapping liquid hazardous waste migration in ground water with electromagnetic terrain conductivity measurement

    International Nuclear Information System (INIS)

    Ketelle, R.H.; Pin, F.G.

    1984-01-01

    Electromagnetic conductivity measurements were used to map apparent ground conductivity in the vicinity of a liquid hazardous waste disposal site. Approximately 600 conductivity measurements were obtained to prepare a conductivity map of the site which includes an area of 12 ha (30 acres). Conductivity measurements in the area correlate with specific conductance measurements of surface and ground water samples. Contouring of the conductivity data located contaminant migration pathways in the subsurface. A complex contaminant plume was defined by the conductivity survey. Conductivity values obtained reflected anisotropic characteristics related to local bedrock structure. Anisotropic characteristics of measurements and the use of different instrument configurations indicated semiquantitatively the depth of the high conductivity zone and the direction of flow. 4 references, 2 figures

  2. Dynamics of soft Nanomaterials captured by transmission electron microscopy in liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Proetto, Maria T.; Rush, Anthony M.; Chien, Miao-Ping; Abellan Baeza, Patricia; Patterson, Joseph P.; Thompson, Matthew P.; Olson, Norman H.; Moore, Curtis E.; Rheingold, Arnold L.; Andolina, Christopher; Millstone, Jill; Howell, Stephen B.; Browning, Nigel D.; Evans, James E.; Gianneschi, Nathan C.

    2014-01-14

    In this paper we present in situ transmission electron microscopy (TEM) of soft, synthetic nanoparticles with a comparative analysis using conventional TEM methods. This comparison is made with the simple aim of describing what is an unprecedented example of in situ imaging by TEM. However, we contend the technique will quickly become essential in the characterization of analogous systems, especially where dynamics are of interest in the solvated state. In this case, particles were studied which were obtained from the direct polymerization of an oxaliplatin analog, designed for an ongoing program in novel chemotherapeutic delivery systems. The resulting nanoparticles provided sufficient contrast for facile imaging in situ, and point toward key design parameters that enable this new characterization approach for organic nanomaterials. We describe the preparation of the synthetic micellar nanoparticles to- gether with their characterization in liquid water.

  3. Radium 226 and uranium isotopes simultaneously determination in water samples using liquid scintillation counter

    International Nuclear Information System (INIS)

    Al-Masri, M.S.; Al-Akel, B.; Saaid, S.; Nashawati, A.

    2007-04-01

    In this work a method has been developed to determine simultaneously Radium 226 and Uranium isotopes in water samples by low back ground Liquid Scintillation Counter. Radium 226 was determined by its progeny Polonium 214 after one month of sample storage in order to achieve the equilibrium between Radium 226 and Polonium 214. Uranium isotopes were determined by subtracting Radium 226 activity from total alpha activity. The method detection limits were 0.049 Bq/L and 0.176 Bq/L for Radium 226 and Uranium isotopes respectively. The repeatability limits were ± 0.32 Bq/L and ± 0.9 Bq/L for Radium 226 and Uranium isotopes respectively. While relative errors were % 9.5 and %18.2 for Radium 226 and Uranium isotopes respectively. On the other hand, the report presented the results of different standard and natural samples.(author)

  4. Switchgrass storage effects on the recovery of carbohydrates after liquid hot water pretreatment and enzymatic hydrolysis

    Directory of Open Access Journals (Sweden)

    Danielle Julie Carrier

    2016-08-01

    Full Text Available Perennial grasses that would be used for bioenergy and bioproducts production will need to be stored for various periods of time to ensure a continual feedstock supply to a bioprocessing facility. The effects of storage practices on grass composition and the response of grasses to subsequent bioprocesses such as pretreatment and enzymatic hydrolysis needs to be understood to develop the most efficient storage protocols. This study examined the effect of outdoor storage of round switchgrass bales on composition before and after liquid hot water pretreatment (LHW and enzymatic hydrolysis. This study also examined the effect of washing LHW pretreated biomass prior to enzymatic hydrolysis. It was determined that switchgrass composition after baling was stable. As expected, glucan and lignin contents increased after LHW due to decreases in xylan and galactan. Washing biomass prior to enzymatic hydrolysis reduced saccharification, especially in samples from the interior of the bale, by at least 5%.

  5. Determination of 90Sr by liquid scintillation spectrometry in samples of contaminated water

    International Nuclear Information System (INIS)

    Ometakova, J.; Dulanska, S.

    2009-01-01

    On a model sample we optimized conditions of SPE separation of 90 Sr on Empore Sr Rad Disk in term of use eluent reagent and its appropriate concentration. Also the possibility of multiple use of both sorbents Empore Sr Rad Disk and AnaLig Sr-01 was confirmed. Not even after 8 separations radiochemical yield fall below 87%. For separation of 90 Sr from real sample of percolating water of controlled area of Bohunice NPP three commercially available products were used: 3M Empore Strontium Rad Disk, sorbents AnaLig (with different grain size) and Sr-Resin. The aim of this work was to compare the selected products in term of strontium extracts, the time demandingness and the possibility of multiple use of sorbents. For separation of strontium were also used two classical methods, namely liquid extraction with tributyl phosphate and carbonate precipitation due to the exclusion of interferents. (author)

  6. A Monte Carlo calculation of subexcitation and vibrationally-relaxing electron spectra in irradiated liquid water

    Energy Technology Data Exchange (ETDEWEB)

    Cobut, V.; Frongillo, Y.; Jay-Gerin, J.-P. (Sherbrooke Univ., PQ (Canada). Faculte de Medecine); Patau, J.-P. (Toulouse-3 Univ., 31 (France))

    1992-12-01

    An energy spectrum of ''subexcitation electrons'' produced in liquid water by electrons with initial energies of a few keV is obtained by using a Monte Carlo transport simulation calculation. It is found that the introduction of vibrational-excitation cross sections leads to the appearance of a sharp peak in the probability density function near the electronic-excitation threshold. Electrons contributing to this peak are shown to be more naturally described if a novel energy spectrum, that we propose to name ''vibrationally-relaxing electron'' spectrum, is introduced. The corresponding distribution function is presented, and an empirical expression of it is given. (author).

  7. Calculated distance distributions of energy transfer events in irradiated liquid water

    International Nuclear Information System (INIS)

    Hamm, R.N.; Turner, J.E.; Wright, H.A.; Ritchie, R.H.

    1980-01-01

    Histories from a Monte Carlo electron transport calculation in liquid water are analyzed to obtain the distance distribution functions, t(x) and T(x), of energy transfer events. These functions, which give the average energy transferred within a distance x from an arbitrary transfer event, are presented for irradiation by monoenergetic electrons of several energies between 500 eV and 1 MeV, for monoenergetic photons of 10, 50, and 200 keV energy and for 65 kVp and 200 kVp x rays and 60 Coγ rays. The dose average lineal energy in spherical sites as a function of site radius is also presented for these same photon spectra

  8. Role of Aquaporin Water Channels in Airway Fluid Transport, Humidification, and Surface Liquid Hydration

    Science.gov (United States)

    Song, Yuanlin; Jayaraman, Sujatha; Yang, Baoxue; Matthay, Michael A.; Verkman, A.S.

    2001-01-01

    Several aquaporin-type water channels are expressed in mammalian airways and lung: AQP1 in microvascular endothelia, AQP3 in upper airway epithelia, AQP4 in upper and lower airway epithelia, and AQP5 in alveolar epithelia. Novel quantitative methods were developed to compare airway fluid transport–related functions in wild-type mice and knockout mice deficient in these aquaporins. Lower airway humidification, measured from the moisture content of expired air during mechanical ventilation with dry air through a tracheotomy, was 54–56% efficient in wild-type mice, and reduced by only 3–4% in AQP1/AQP5 or AQP3/AQP4 double knockout mice. Upper airway humidification, measured from the moisture gained by dry air passed through the upper airways in mice breathing through a tracheotomy, decreased from 91 to 50% with increasing ventilation from 20 to 220 ml/min, and reduced by 3–5% in AQP3/AQP4 knockout mice. The depth and salt concentration of the airway surface liquid in trachea was measured in vivo using fluorescent probes and confocal and ratio imaging microscopy. Airway surface liquid depth was 45 ± 5 μm and [Na+] was 115 ± 4 mM in wild-type mice, and not significantly different in AQP3/AQP4 knockout mice. Osmotic water permeability in upper airways, measured by an in vivo instillation/sample method, was reduced by ∼40% by AQP3/AQP4 deletion. In doing these measurements, we discovered a novel amiloride-sensitive isosmolar fluid absorption process in upper airways (13% in 5 min) that was not affected by aquaporin deletion. These results establish the fluid transporting properties of mouse airways, and indicate that aquaporins play at most a minor role in airway humidification, ASL hydration, and isosmolar fluid absorption. PMID:11382807

  9. Possibilities of practical usage of dispersed aluminim oxidation by liquid water

    Science.gov (United States)

    Larichev, M. N.; Laricheva, O. O.; Shaitura, N. S.; Shkolnikov, E. I.

    2012-12-01

    The goal of this work is to show the possibility of practical usage of the environmentally pure oxidation process of preliminarily dispersed aluminum (aluminum powders of the ASD or PAD grade according to TU (Technical Specifications) 48-5-226-87, which are serially produced in industry) with liquid water in order to obtain gaseous hydrogen in volumes sufficient to provide the operation of energizers based on airhydrogen fuel cells (AHFC) for portable and stationary devices (up to 3 kW). It is shown that the synthesis of aluminum oxides-hydroxides with the specified phase and chemical compositions as well as the particle shape and size can be provided simultaneously with producing commercial hydrogen. The practical usage of hydrogen, which is formed in the oxidation reaction of metallic aluminum with liquid water at pressures close to atmospheric (particularly, to service AHFCs), requires reaction intensification to increase the oxidation rate of aluminum. In this work, we considered the aspects of practical implementation of thermal, ultrasonic, and chemical activation as well as their combinations for this purpose. As the chemical activator of oxidation, we used the additives of calcium oxide (<5% of the mass of oxidized aluminum). Application of each activation method affects the phase and chemical compositions as well as the structure of formed aluminum hydroxides, which provides the possibility of their reproducible production. Thus, simultaneously with the production of commercial hydrogen, solid oxidation products satisfying the needs of industry in aluminum oxides and having the specified composition, purity, and particle shape and size can be synthesized. The acquired experimental results and elements of the design of specially developed industrial apparatuses, which were used when performing this work, can be applied when designing the model of the hydrogen generator—the prototype of the hydrogen generator for portable and stationary devices or devices

  10. Applications, features, and mechanistic aspects of liquid water beam desorption mass spectrometry

    Science.gov (United States)

    Abel, B.; Charvat, A.; Diederichsen, U.; Faubel, M.; Girmann, B.; Niemeyer, J.; Zeeck, A.

    2005-05-01

    In the present study we highlight recent applications of liquid beam desorption mass spectrometry for the analysis of biomolecules. The protonated macromolecules are desorbed from a 10 [mu]m thick liquid jet in vacuum with an IR laser pulse tuned in resonance with the OH stretch vibration of water. Cytochrome c, viscotoxin A3, synthetic analogues of DNA and nucleobase substituted [beta]-peptides (PNA like oligomers), bovine serum albumin (BSA), as well as specifically designed pharmaceutical macromolecules have been investigated. The salt and buffer tolerance has been measured for the desorption of cytochrome c. For the PNA oligomers it has been shown that a mixture can be desorbed and that the relative intensity of the mass peaks reflects relative concentrations in solution. With diluted BSA water solutions it has been demonstrated that the desorption technique provides a quantitative measure of BSA in solution. The gas phase signal of singly protonated BSA desorbed from a series of well defined solution concentrations has been found to be linear over at least three orders of magnitude. This feature appears to be promising for quantitative online monitoring applications of this technique. Beyond applications of this technique mechanistic aspects of the poorly characterized desorption mechanism are discussed. With a field-free-drift time-of-flight approach we were able to monitor features of the desorption process by selecting fractions of the broad velocity distribution of desorbed species using an ion optics acting as an ion gate. The observed features were discussed within a "desorption/ionization" model featuring the interplay of an explosive thermal and a shock wave dispersion of the microfilament controlling the ejection of hot nano-droplets and microsolvated molecules as well as their desolvation.

  11. Water level response measurement in a steel cylindrical liquid storage tank using image filter processing under seismic excitation

    Science.gov (United States)

    Kim, Sung-Wan; Choi, Hyoung-Suk; Park, Dong-Uk; Baek, Eun-Rim; Kim, Jae-Min

    2018-02-01

    Sloshing refers to the movement of fluid that occurs when the kinetic energy of various storage tanks containing fluid (e.g., excitation and vibration) is continuously applied to the fluid inside the tanks. As the movement induced by an external force gets closer to the resonance frequency of the fluid, the effect of sloshing increases, and this can lead to a serious problem with the structural stability of the system. Thus, it is important to accurately understand the physics of sloshing, and to effectively suppress and reduce the sloshing. Also, a method for the economical measurement of the water level response of a liquid storage tank is needed for the exact analysis of sloshing. In this study, a method using images was employed among the methods for measuring the water level response of a liquid storage tank, and the water level response was measured using an image filter processing algorithm for the reduction of the noise of the fluid induced by light, and for the sharpening of the structure installed at the liquid storage tank. A shaking table test was performed to verify the validity of the method of measuring the water level response of a liquid storage tank using images, and the result was analyzed and compared with the response measured using a water level gauge.

  12. Magnetical hollow fiber bar collection of extract in homogenous ionic liquid microextraction of triazine herbicides in water samples.

    Science.gov (United States)

    Wang, Kun; Jiang, Jia; Kang, Mingqin; Li, Dan; Zang, Shuang; Tian, Sizhu; Zhang, Hanqi; Yu, Aimin; Zhang, Ziwei

    2017-04-01

    The homogeneous ionic liquid microextraction combined with magnetical hollow fiber bar collection was developed for extracting triazine herbicides from water samples. These analytes were separated and determined by high performance liquid chromatography. The triazines were quickly extracted into ionic liquid microdroplets dispersed in solution, and then these microdroplets were completely collected with magnetical hollow fiber bars; the pores of which were impregnated with hydrophobic ionic liquid, which makes the phase separation simplified with no need of centrifugation. Some experimental parameters, such as the type of ionic liquid, ultrasonic immersion time of hollow fiber, pH of sample solution, volume of hydrophilic ionic liquid, amount of ion-pairing agent NH 4 PF 6 , NaCl concentration, number of magnetical hollow fiber bar, stirring rate, and collection time were investigated and optimized. When the present method was applied to the analysis of real water samples, the precision and recoveries of six triazine herbicides vary from 0.1 to 9.2% and 73.4 to 118.5%, respectively. The detection limits for terbumeton, ametryn, prometryn, terbutryn, trietazine, and dimethametryn were 0.48, 0.15, 0.15, 0.14, 0.35, and 0.16 μg L -1 , respectively.

  13. Application of artificial neural network for vapor liquid equilibrium calculation of ternary system including ionic liquid: Water, ethanol and 1-butyl-3-methylimidazolium acetate

    Energy Technology Data Exchange (ETDEWEB)

    Fazlali, Alireza; Koranian, Parvaneh [Arak University, Arak (Iran, Islamic Republic of); Beigzadeh, Reza [Islamic Azad University, Kermanshah (Iran, Islamic Republic of); Rahimi, Masoud [Razi University, Kermanshah (Iran, Islamic Republic of)

    2013-09-15

    A feed forward three-layer artificial neural network (ANN) model was developed for VLE prediction of ternary systems including ionic liquid (IL) (water+ethanol+1-butyl-3- methyl-imidazolium acetate), in a relatively wide range of IL mass fractions up to 0.8, with the mole fractions of ethanol on IL-free basis fixed separately at 0.1, 0.2, 0.4, 0.6, 0.8, and 0.98. The output results of the ANN were the mole fraction of ethanol in vapor phase and the equilibrium temperature. The validity of the model was evaluated through a test data set, which were not employed in the training case of the network. The performance of the ANN model for estimating the mole fraction and temperature in the ternary system including IL was compared with the non-random-two-liquid (NRTL) and electrolyte non-random-two- liquid (eNRTL) models. The results of this comparison show that the ANN model has a superior performance in predicting the VLE of ternary systems including ionic liquid.

  14. Application of artificial neural network for vapor liquid equilibrium calculation of ternary system including ionic liquid: Water, ethanol and 1-butyl-3-methylimidazolium acetate

    International Nuclear Information System (INIS)

    Fazlali, Alireza; Koranian, Parvaneh; Beigzadeh, Reza; Rahimi, Masoud

    2013-01-01

    A feed forward three-layer artificial neural network (ANN) model was developed for VLE prediction of ternary systems including ionic liquid (IL) (water+ethanol+1-butyl-3- methyl-imidazolium acetate), in a relatively wide range of IL mass fractions up to 0.8, with the mole fractions of ethanol on IL-free basis fixed separately at 0.1, 0.2, 0.4, 0.6, 0.8, and 0.98. The output results of the ANN were the mole fraction of ethanol in vapor phase and the equilibrium temperature. The validity of the model was evaluated through a test data set, which were not employed in the training case of the network. The performance of the ANN model for estimating the mole fraction and temperature in the ternary system including IL was compared with the non-random-two-liquid (NRTL) and electrolyte non-random-two- liquid (eNRTL) models. The results of this comparison show that the ANN model has a superior performance in predicting the VLE of ternary systems including ionic liquid

  15. Towards a unified description of the hydrogen bond network of liquid water: A dynamics based approach

    International Nuclear Information System (INIS)

    Ozkanlar, Abdullah; Zhou, Tiecheng; Clark, Aurora E.

    2014-01-01

    The definition of a hydrogen bond (H-bond) is intimately related to the topological and dynamic properties of the hydrogen bond network within liquid water. The development of a universal H-bond definition for water is an active area of research as it would remove many ambiguities in the network properties that derive from the fixed definition employed to assign whether a water dimer is hydrogen bonded. This work investigates the impact that an electronic-structure based definition, an energetic, and a geometric definition of the H-bond has upon both topological and dynamic network behavior of simulated water. In each definition, the use of a cutoff (either geometric or energetic) to assign the presence of a H-bond leads to the formation of transiently bonded or broken dimers, which have been quantified within the simulation data. The relative concentration of transient species, and their duration, results in two of the three definitions sharing similarities in either topological or dynamic features (H-bond distribution, H-bond lifetime, etc.), however no two definitions exhibit similar behavior for both classes of network properties. In fact, two networks with similar local network topology (as indicated by similar average H-bonds) can have dramatically different global network topology (as indicated by the defect state distributions) and altered H-bond lifetimes. A dynamics based correction scheme is then used to remove artificially transient H-bonds and to repair artificially broken bonds within the network such that the corrected network exhibits the same structural and dynamic properties for two H-bond definitions (the properties of the third definition being significantly improved). The algorithm described represents a significant step forward in the development of a unified hydrogen bond network whose properties are independent of the original hydrogen bond definition that is employed

  16. Advanced control of liquid water region in diffusion media of polymer electrolyte fuel cells through a dimensionless number

    Science.gov (United States)

    Wang, Yun; Chen, Ken S.

    2016-05-01

    In the present work, a three-dimension (3-D) model of polymer electrolyte fuel cells (PEFCs) is employed to investigate the complex, non-isothermal, two-phase flow in the gas diffusion layer (GDL). Phase change in gas flow channels is explained, and a simplified approach accounting for phase change is incorporated into the fuel cell model. It is found that the liquid water contours in the GDL are similar along flow channels when the channels are subject to two-phase flow. Analysis is performed on a dimensionless parameter Da0 introduced in our previous paper [Y. Wang and K. S. Chen, Chemical Engineering Science 66 (2011) 3557-3567] and the parameter is further evaluated in a realistic fuel cell. We found that the GDL's liquid water (or liquid-free) region is determined by the Da0 number which lumps several parameters, including the thermal conductivity and operating temperature. By adjusting these factors, a liquid-free GDL zone can be created even though the channel stream is two-phase flow. Such a liquid-free zone is adjacent to the two-phase region, benefiting local water management, namely avoiding both severe flooding and dryness.

  17. Phase equilibria for ternary liquid systems of (water + levulinic acid + cyclic solvent) at T = 298.2 K: Thermodynamic modeling

    Energy Technology Data Exchange (ETDEWEB)

    Senol, Aynur [Istanbul University, Faculty of Engineering, Department of Chemical Engineering, 34320 Avcilar, Istanbul (Turkey)]. E-mail: senol@istanbul.edu.tr

    2005-10-15

    (Liquid + liquid) equilibrium (LLE) data of the solubility curves and tie-line end compositions are presented for mixtures of {l_brace}water (1) + levulinic acid (2) + methylcyclohexanol, or cyclohexanone, or cyclohexyl acetate (3){r_brace} at T = 298.2 K and P = (101.3 {+-} 0.7) kPa. Among the studied C6 ring-containing cyclic solvents, methylcyclohexanol and cyclohexyl acetate give the largest distribution ratio and separation factors for extraction of levulinic acid. A solvation energy relation (SERLAS) has been used to estimate the (liquid + liquid) equilibria of associated systems containing components capable of a physical interaction through hydrogen bonding. The tie-lines were also predicted using the UNIFAC-original model. The reliability of both models has been analyzed against the LLE data with respect to the distribution ratio and separation factor. SERLAS matches LLE data quite accurately, yielding a mean error of 3.6% for all the systems considered.

  18. Phase equilibria for ternary liquid systems of (water + tetrahydrofuran + nonprotic aromatic solvent) at T = 298.2 K

    Energy Technology Data Exchange (ETDEWEB)

    Senol, Aynur [Istanbul University, Faculty of Engineering, Department of Chemical Engineering, 34320 Avcilar, Istanbul (Turkey)]. E-mail: senol@istanbul.edu.tr; Sevgili, Lutfullah [Istanbul University, Faculty of Engineering, Department of Chemical Engineering, 34320 Avcilar, Istanbul (Turkey)

    2006-05-15

    (Liquid + liquid) equilibrium (LLE) data of the solubility curves and tie-line end compositions are presented for mixtures of {l_brace}water (1) + tetrahydrofuran (2) + xylene or chlorobenzene or benzyl ether (3){r_brace} at T = 298.2 K and P = (101.3 {+-} 0.7) kPa. Among the studied C6 ring-containing aromatic solvents, xylene gives the largest distribution ratio and separation factors for extraction of tetrahydrofuran. A solvation energy relation (SERLAS) has been used to estimate the (liquid + liquid) equilibria of associated systems containing a nonprotic solvent. The tie-lines were also predicted using the UNIFAC-original model. The reliability of both models has been analyzed against the LLE data with respect to the distribution ratio and separation factor. SERLAS matches LLE data accurately, yielding a mean error of 9.9% for all the systems considered.

  19. Dispersive liquid-liquid microextraction based on solidification of floating organic droplet for the determination of triazine and triazoles in mineral water samples.

    Science.gov (United States)

    Bolzan, Cátia M; Caldas, Sergiane S; Guimarães, Bruno S; Primel, Ednei G

    2016-09-01

    A simple, rapid, and sensitive method for the determination of atrazine, simazine, cyproconazole, tebuconazole, and epoxiconazole in mineral water employing the dispersive liquid-liquid microextraction with solidification of a floating organic drop with determination by liquid chromatography tandem mass spectrometry has been developed. A mixed solution of 250 μL 1-dodecanol and 1250 μL methanol was injected rapidly into 10 mL aqueous solution (pH 7.0) with 2% w/v NaCl. After centrifugation for 5 min at 2000 rpm, the organic solvent droplets floated on the surface of the aqueous solution and the floating solvent solidified. The method limits of detection were between 3.75 and 37.5 ng/L and limits of quantification were between 12.5 and 125 ng/L. The recoveries ranged from 70 to 118% for repeatability and between 76 and 95% for intermediate precision with a relative standard deviation from 2 to 18% for all compounds. Low matrix effect was observed. The proposed method can be successfully applied in routine analysis for determination of pesticide residues in mineral water samples, allowing for monitoring of triazine and triazoles at levels below the regulatory limits set by international and national legislations. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Efficient capture of SO2 by a binary mixture of caprolactam tetrabutyl ammonium bromide ionic liquid and water.

    Science.gov (United States)

    Duan, Erhong; Guo, Bin; Zhang, Miaomiao; Guan, Yanan; Sun, Hua; Han, Jing

    2011-10-30

    The solubility of SO(2) in a binary mixture of water and caprolactam tetrabutyl ammonium bromide ionic liquid (CPL-TBAB IL) was investigated. Though the ionic liquid and water were fully miscible, a phase separation occurred when SO(2) was introduced into the mixture. The SO(2) concentrated in the lower layer, and it could be released by heating the solution under reduced pressure (382.2K, 10.1 kPa). After desorption, the mixture could be reused to absorb SO(2). It was found that SO(2) acts as a switch to cause the water and CPL-TBAB IL to phase separate, and the mechanics of this phase separation process was studied by gas chromatography-mass spectrometry, fourier transform-infrared spectroscopy and Karl-Fisher titration. The absorption and desorption of SO(2) in the CPL-TBAB/water mixtures were reversible. Copyright © 2011 Elsevier B.V. All rights reserved.

  1. Stabilized liquid membrane device (SLMD) for the passive, integrative sampling of labile metals in water

    Science.gov (United States)

    Brumbaugh, W.G.; Petty, J.D.; Huckins, J.N.; Manahan, S.E.

    2002-01-01

    A stabilized liquid membrane device (SLMD) is described for potential use as an in situ, passive, integrative sampler for cadmium (Cd), cobalt (Co), copper (Cu), nickel (Ni), lead (Pb), and zinc (Zn) in natural waters. The SLMD (patent pending) consists of a 2.5-cm-wide by 15-cm-long strip of low-density polyethylene (LDPE) layflat tubing containing 1 mL of an equal mixture (v/v) of oleic acid (cis-9-octadecenoic acid) and EMO-8Q (7-[4-ethyl-1-methyloctyl]-8-quinolinol). The reagent mixture continuously diffuses to the exterior surface of the LDPE membrane, and provides for sequestration of several divalent metals for up to several weeks. Depending on sampler configuration, concentration factors of several thousand can be realized for these metal ions after just a few days. In addition to in situ deployment, the SLMD may be useful for laboratory determination of labile metal species in grab samples. Methods for minimizing the effects of water flow on the sampling rate are currently under investigation.

  2. Modeling proton and alpha elastic scattering in liquid water in Geant4-DNA

    Energy Technology Data Exchange (ETDEWEB)

    Tran, H.N., E-mail: tranngochoang@tdt.edu.vn [Division of Nuclear Physics, Ton Duc Thang University, Tan Phong Ward, District 7, Ho Chi Minh City (Viet Nam); Faculty of Applied Sciences, Ton Duc Thang University, Tan Phong Ward, District 7, Ho Chi Minh City (Viet Nam); El Bitar, Z. [Institut Pluridisciplinaire Hubert Curien/IN2P3/CNRS, Strasbourg (France); Champion, C. [Univ. Bordeaux, CENBG, UMR 5797, F-33170 Gradignan (France); CNRS, IN2P3, CENBG, UMR 5797, F-33170 Gradignan (France); Karamitros, M. [Univ. Bordeaux, CENBG, UMR 5797, F-33170 Gradignan (France); CNRS, IN2P3, CENBG, UMR 5797, F-33170 Gradignan (France); CNRS, INCIA, UMR 5287, F-33400 Talence (France); Bernal, M.A. [Instituto de FísicaGleb Wataghin, Universida de Estadual de Campinas, SP (Brazil); Francis, Z. [Université Saint Joseph, Faculty of Science, Department of Physics, Beirut (Lebanon); The Open University, Faculty of Science, Department of Physical Sciences, Walton Hall, MK7 6AA Milton Keynes (United Kingdom); Ivantchenko, V. [Ecoanalytica, 119899 Moscow (Russian Federation); Lee, S.B.; Shin, J.I. [Proton Therapy Center, National Cancer Center, 323 Ilsan-ro, Ilsandong-gu, Goyang-si, Gyeonggi-do 410-769 (Korea, Republic of); Incerti, S. [Univ. Bordeaux, CENBG, UMR 5797, F-33170 Gradignan (France); CNRS, IN2P3, CENBG, UMR 5797, F-33170 Gradignan (France)

    2015-01-15

    Elastic scattering of protons and alpha (α) particles by water molecules cannot be neglected at low incident energies. However, this physical process is currently not available in the “Geant4-DNA” extension of the Geant4 Monte Carlo simulation toolkit. In this work, we report on theoretical differential and integral cross sections of the elastic scattering process for 100 eV–1 MeV incident protons and for 100 eV–10 MeV incident α particles in liquid water. The calculations are performed within the classical framework described by Everhart et al., Ziegler et al. and by the ICRU 49 Report. Then, we propose an implementation of the corresponding classes into the Geant4-DNA toolkit for modeling the elastic scattering of protons and α particles. Stopping powers as well as ranges are also reported. Then, it clearly appears that the account of the elastic scattering process in the slowing-down of the charged particle improves the agreement with the existing data in particular with the ICRU recommendations.

  3. Simultaneous detection of water-soluble vitamins using the High Performance Liquid Chromatography (HPLC - a review

    Directory of Open Access Journals (Sweden)

    Rosemond Godbless Dadzie

    2014-01-01

    Full Text Available The water-soluble vitamins (WSV: ascorbic acid (vitamin C, thiamine (B1, riboflavin (B2, niacin (B3, panthothenic acid (B5, pyridoxine, and pyridoxal (B6, folic acid (B9, biotin(B8 , and B12 are very essential in the diet of humankind. As a result of ever increasing pressures from both consumers and legal enforcers, to specify accurately nutritive compositions of WSV that are present in food materials, many researchers have attempted to fill this niche through the provision of highly sensitive and rapid high performance liquid chromatography (HPLC procedures. In view of the health benefits of WSV, a replete of HPLC methods have been developed for simultaneous determination of their contents in nature and fortified food samples, nutritional supplements, as well as blood plasmas. The rate of losses of these vitamins during food processing and analysis, in addition to their transient dynamics, presents complexities in developing a highly sensitive HPLC procedure for their simultaneous separations and assays. This review critically assesses the different HPLC procedures developed by researchers and available in the open literature for simultaneous determination of water-soluble vitamins (WSV in dried tropical fruits materials. The study revealed that not a single chromatographic run developed by researchers can simultaneously elute all the WSV at a time. However, the HPLC procedures that are capable of determining all the WSV were coupled with electrospray ionization mass spectroscopy (ESI-MS, thus making the set-up expensive.

  4. Measurement of radon-222 and radium-226 in ground water by liquid scintillation counting

    Energy Technology Data Exchange (ETDEWEB)

    Herczeg, A.L.; Dighton, J.C.; Easterbrook, M.L.; Salomons, E. [Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT (Australia). Div. of Water Resources Research

    1994-12-31

    A pilot study was carried out to establish the hydrogeological controls on radon and radium concentrations in potable groundwaters from selected aquifer types throughout Australia. The draft AWRC/SHMRC drinking water guidelines specify a recommended value of 100 BqL{sup -1} for Rn-222 and 0.5 BqL{sup -1} for Ra-226 and Ra-228. Preliminary measurements in groundwater indicate enormous variability for Rn-222 concentrations; from 10 BqL{sup -1} in limestone to 500 BqL{sup -1} in granitic and high grade metamorphic fractured rock systems. The associated Ra-226 concentrations are much lower (<0.5 BqL{sup -1}). Measurements are carried out using the LKB Wallac Quantulus liquid scintillation counter which has an overall efficiency of >250% for radon and it`s short lived {alpha} emitting progeny. Background count rates are around 0.7 cpm. Figure of merit (E{sup 2}/B) values of around 10 000 are obtained using NEN High Efficiency Mineral Oil cocktail to water sample ratios of 2:1. These figures concur with findings in Europe and North America regarding prelevance of high radon concentrations in hard-rock formation. 8 refs., 1 tab., 1 fig.

  5. Laboratory study of non-aqueous phase liquid and water co-boiling during thermal treatment.

    Science.gov (United States)

    Zhao, C; Mumford, K G; Kueper, B H

    2014-08-01

    In situ thermal treatment technologies, such as electrical resistance heating and thermal conductive heating, use subsurface temperature measurements in addition to the analysis of soil and groundwater samples to monitor remediation performance. One potential indication of non-aqueous phase liquid (NAPL) removal is an increase in temperature following observations of a co-boiling plateau, during which subsurface temperatures remain constant as NAPL and water co-boil. However, observed co-boiling temperatures can be affected by the composition of the NAPL and the proximity of the NAPL to the temperature measurement location. Results of laboratory heating experiments using single-component and multi-component NAPLs showed that local-scale temperature measurements can be mistakenly interpreted as an indication of the end of NAPL-water co-boiling, and that significant NAPL saturations (1% to 9%) remain despite observed increases in temperature. Furthermore, co-boiling of multi-component NAPL results in gradually increasing temperature, rather than a co-boiling plateau. Measurements of gas production can serve as a complementary metric for assessing NAPL removal by providing a larger-scale measurement integrated over multiple smaller-scale NAPL locations. Measurements of the composition of the NAPL condensate can provide ISTT operators with information regarding the progress of NAPL removal for multi-component sources. Copyright © 2014 Elsevier B.V. All rights reserved.

  6. Importance of soil heating, liquid water loss, and vapor flow enhancement for evaporation

    Science.gov (United States)

    Novak, Michael D.

    2016-10-01

    Field measurements conducted by Cahill and Parlange (1998) are reanalyzed to verify if their conclusion that daytime peak values of 60-70 W m-2 of latent heat flux divergence occurred in the 7-10 cm soil layer of a drying Yolo silt loam when maximum values of surface latent heat flux are estimated to have been about 100 W m-2. The new analyses, as similar to theirs as possible, are validated using a numerical simulation of coupled soil moisture and heat flow based on Philip and de Vries (1957) as a test bed. The numerical simulation is extended to include the flow of air induced by diurnal soil heating and evaporative water loss to verify the flux divergence calculations reported in Parlange et al. (1998) that explained the findings of Cahill and Parlange (1998). It is shown that the conclusions of both of these papers are in error, so that the original version of the Philip and de Vries (1957) theory is consistent with their field measurements after all and the effects of airflow associated with soil heating and liquid water loss (and low-frequency barometric pressure variations also considered) are negligible in practice. In an additional investigation, enhancement of diffusive vapor flow (first postulated by Philip and de Vries (1957)) and discussed extensively in the literature since is shown to have negligible effects on cumulative evaporation under field conditions.

  7. Carbohydrates-tailored phase tunable systems composed of ionic liquids and water

    International Nuclear Information System (INIS)

    Chen Yuhaun; Wang Yige; Cheng Qingyan; Liu Xiaoli; Zhang Suojiang

    2009-01-01

    Carbohydrates were found to have substantial effects on tailoring phase tunable of ionic liquids (ILs) and water. Phase behaviors of 1-alkyl-3-methylimidazolium derivatives [C n mim]X (n = 2 to 10, X = Cl - , Br - , BF 4 - )-carbohydrate-H 2 O were systemically investigated. For hydrophilic ILs, 1-alkyl-3-methylimidazolium tetrafluoroborate [C n mim]BF 4 (n = 3, 4), the homogeneous aqueous solution can be induced to separate two aqueous phases by addition of carbohydrate. For hydrophobic ILs, [C n mim]BF 4 (n = 5 to 10), the mutual solubility with water can be lowered by addition of carbohydrate. While 1-alkyl-3-methyl imidazolium chloride ([C n mim]Cl, n = 2 to 10) and 1-alkyl-3-methyl imidazolium bromide ([C n mim]Br, n = 2 to 10) aqueous solutions never form aqueous two-phase systems (ATPSs) with carbohydrate in the investigated temperatures ranging from (242.15 to 373.15) K. The high partitioning behavior of phenol in [C n mim]BF 4 (n = 3 to 10) (1) + carbohydrate (2) + H 2 O (3) shows that carbohydrate-tailored {IL + H 2 O} systems are feasible to be used as extraction systems, especially in biological and environmental engineering.

  8. Effect of cationic surfactants on organic liquid-water capillary pressure-saturation relationships

    Science.gov (United States)

    Demond, A. H.; Desai, F. N.; Hayes, K. F.

    1994-02-01

    Many solutes, either naturally occurring or introduced, are surface active and sorb preferentially at the interfaces of subsurface systems. In multiphase systems, the sorption of surfactants affects the capillary pressure-saturation relationships, fundamental constitutive relationships in the modeling of multiphase flow. In this study, the impact of surfactant sorption on capillary pressure relationships for organic liquid-waters systems was demonstrated by qualitatively correlating measurements of sorption and zeta potential, with interfacial tension and contact angle and, in turn, quantitatively relating these measurements to changes in capillary pressure-saturation relationships for o-xylene-water-quartz systems containing a cationic surfactant, cetyltrimethylammonium bromide (CTAB). The results show that the sorption of CTAB causes the naturally hydrophilic system to become hydrophobic, as evidenced by a change in the contact angle from about 10°-15° to 155° or 180°, depending on the pH. This change in hydrophilicity is reflected in the zeta potential of the system which goes from negative to positive as the aqueous phase CTAB concentration increases. The spontaneous imbibition capillary pressure-saturation relationship is more sensitive to the sorption of CTAB than the drainage relationship. To predict the observed changes in both capillary pressure-saturation relationships, a modified form of Leverett's function was used where roughness and curvature corrections were incorporated into the intrinsic contact angle to give an operational contact angle. A comparison of the measured and predicted capillary pressure-saturation relationships showed reasonable agreement.

  9. Vapor-liquid equilibria for nitric acid-water and plutonium nitrate-nitric acid-water solutions

    International Nuclear Information System (INIS)

    Maimoni, A.

    1980-01-01

    The liquid-vapor equilibrium data for nitric acid and nitric acid-plutnonium nitrate-water solutions were examined to develop correlations covering the range of conditions encountered in nuclear fuel reprocessing. The scanty available data for plutonium nitrate solutions are of poor quality but allow an order of magnitude estimate to be made. A formal thermodynamic analysis was attempted initially but was not successful due to the poor quality of the data as well as the complex chemical equilibria involved in the nitric acid and in the plutonium nitrate solutions. Thus, while there was no difficulty in correlating activity coefficients for nitric acid solutions over relatively narrow temperature ranges, attempts to extend the correlations over the range 25 0 C to the boiling point were not successful. The available data were then analyzed using empirical correlations from which normal boiling points and relative volatilities can be obtained over the concentration ranges 0 to 700 g/l Pu, 0 to 13 M nitric acid. Activity coefficients are required, however, if estimates of individual component vapor pressures are needed. The required ternary activity coefficients can be approximated from the correlations

  10. In situ metathesis reaction combined with liquid-phase microextraction based on the solidification of sedimentary ionic liquids for the determination of pyrethroid insecticides in water samples.

    Science.gov (United States)

    Hu, Lu; Zhang, Panjie; Shan, Wanyu; Wang, Xuan; Li, Songqing; Zhou, Wenfeng; Gao, Haixiang

    2015-11-01

    A novel dispersion liquid-liquid microextraction method based on the solidification of sedimentary ionic liquids (SSIL-DLLME), in which an in situ metathesis reaction forms an ionic liquid (IL) extraction phase, was developed to determine four pyrethroid insecticides (i.e., permethrin, cyhalothrin, fenpropathrin, and transfluthrin) in water followed by separation using high-performance liquid chromatography. In the developed method, in situ DLLME was used to enhance the extraction efficiency and yield. After centrifugation, the extraction solvent, tributyldodecylphosphonium hexafluorophosphate ([P44412][PF6]), was easily collected by solidification in the bottom of the tube. The effects of various experimental parameters, the quantity of tributyldodecylphosphonium bromide ([P44412]Br), the molar ratio of [P44412]Br to potassium hexafluorophosphate (KPF6), the ionic strength, the temperature of the sample solution, and the centrifugation time, were optimized using a Plackett-Burman design to identify the significant factors that affected the extraction efficiency. These significant factors were then optimized using a central composite design. Under the optimized conditions, the recoveries of the four pyrethroid insecticides at four spiked levels ranged from 87.1% to 101.7%, with relative standard deviations (RSDs) ranging from 0.1% to 5.5%. At concentration levels between 1 and 500 µg/L, good linearity was obtained, with coefficients of determination greater than 0.9995. The limits of detection (LODs) for the four pyrethroid insecticides were in the range of 0.71-1.54 µg/L. The developed method was then successfully used for the determination of pyrethroid insecticides in environmental samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Synthesis of glucaminium-based ionic liquids and their application in the removal of boron from water.

    Science.gov (United States)

    Joshi, Manishkumar D; Chalumot, Guillaume; Kim, Yong-wah; Anderson, Jared L

    2012-02-01

    A novel class of ionic liquids (ILs), exhibiting high selectivity towards boron species as well as the ability to phase separate from water, were synthesized from N-methyl-D-glucamine. The complexation of boric acid/borate with the ILs was confirmed using (11)B NMR. This journal is © The Royal Society of Chemistry 2012

  12. Isothermal Vapor-Liquid Equilibrium in the Quaternary Water + 2-Propanol + Acetic Acid + Isopropyl Acetate System with Chemical Reaction

    Czech Academy of Sciences Publication Activity Database

    Teodorescu, M.; Aim, Karel; Wichterle, Ivan

    2001-01-01

    Roč. 46, č. 2 (2001), s. 261-266 ISSN 0021-9568 R&D Projects: GA ČR GA203/98/1446 Institutional research plan: CEZ:AV0Z4072921 Keywords : vapor-liquid equilibrium * quaternary water Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 0.960, year: 2001

  13. A green and facile approach for the synthesis of water-dispersible reduced graphene oxide based on ionic liquids.

    Science.gov (United States)

    Zhang, Tongping; Liu, Ping; Sheng, Chunrui; Duan, Yongxin; Zhang, Jianming

    2014-03-18

    A green and facile route for producing reduced graphene oxide based on ionic liquids has been proposed, in which the as-prepared graphene can be redispersed stably in water (up to 0.6 mg mL(-1)) after being made into a flow-directed solid film.

  14. Solid-liquid phase transition in a Gibbs monolayer of melissic acid at the n-hexane-water interface

    Science.gov (United States)

    Tikhonov, A. M.

    2015-10-01

    A sharp phase transition from a crystalline state with the area per molecule A = (17 ± 1) Å2 to a liquid state with A = (23 ± 1) Å2 at the n-hexane-water interface in a Gibbs monolayer of melissic acid has been revealed in data of X-ray reflectometry with the use of synchrotron radiation.

  15. Ultrasound-air-assisted demulsified liquid-liquid microextraction by solidification of a floating organic droplet for determination of three antifungal drugs in water and biological samples.

    Science.gov (United States)

    Ezoddin, Maryam; Shojaie, Mehran; Abdi, Khosrou; Karimi, Mohammad Ali

    2017-03-01

    A novel ultrasound-air-assisted demulsified liquid-liquid microextraction by solidification of a floating organic droplet (UAAD-LLM-SFO) followed by HPLC-UV detection was developed for the analysis of three antifungal drugs in water and biological samples. In this method, 1-dodecanol was used as the extraction solvent. The emulsion was rapidly formed by pulling in and pushing out the mixture of sample solution and extraction solvent for 5 times repeatedly using a 10-mL glass syringe while sonication was performed. Therefore, an organic dispersive solvent required in common microextraction methods was not used in the proposed method. After dispersing, an aliquot of acetonitrile was introduced as a demulsifier solvent into the sample solution to separate two phases. Therefore, some additional steps, such as the centrifugation, ultrasonication, or agitation of the sample solution, are not needed. Parameters influencing the extraction recovery were investigated. The proposed method showed a good linearity for the three antifungal drugs studied with the correlation coefficients (R 2  > 0.9995). The limits of detection (LODs) and the limits of the quantification (LOQs) were between 0.01-0.03 μg L -1 and 0.03-0.08 μg L -1 , respectively. The preconcentration factors (PFs) were in the range of 107-116, respectively. The precisions, as the relative standard deviations (RSDs) (n = 5), for inter-day and intra-day analysis were in the range of 2.1-4.5% and 6.5-8.5%, respectively. This method was successfully applied to determine the three antifungal drugs in tap water and biological samples. The recoveries of antifungal drugs in these samples were 92.4-98.5%. Graphical abstract Ultrasound-air-assisted demulsified liquid-liquid microextraction by solidification of a floating organic droplet for the analysis of three antifungal drugs prior HPLC-UV.

  16. Isobaric vapour-liquid-liquid equilibrium and vapour-liquid equilibrium for the system water + ethanol + iso-octane at 101.3 kPa

    OpenAIRE

    Ruiz Beviá, Francisco; Gomis Yagües, Vicente; Asensi Steegmann, Juan Carlos; Font Escamilla, Alicia

    2002-01-01

    Poster enviado a Equifase 2002, VI Iberoamerican Conference on Phase Equilibria for Process Design, Foz de Iguazú (Brazil), October 12th to 16th, 2002. Many studies have been carried out in the heterogeneous azeotropic distillation field either by experiment or by simulation. The development of all these studies requires the use of sets of isobaric vapour–liquid–liquid equilibrium (VLLE) data. However, the number of ternary systems with experimental VLLE data is very limited, since it is d...

  17. Liquid methane gelled with methanol and water reduces rate of nitrogen absorption

    Science.gov (United States)

    Vanderwall, E. M.

    1972-01-01

    Dilution of gelant vapor with inert carrier gas accomplishes gelation. Mixture is injected through heated tube and orifice into liquid methane for immediate condensation within bulk of liquid. Direct dispersion of particles in liquid avoids condensation on walls of vessel and eliminates additional mixing.

  18. Cognitive Approaches for Medicine in Cloud Computing.

    Science.gov (United States)

    Ogiela, Urszula; Takizawa, Makoto; Ogiela, Lidia

    2018-03-03

    This paper will present the application potential of the cognitive approach to data interpretation, with special reference to medical areas. The possibilities of using the meaning approach to data description and analysis will be proposed for data analysis tasks in Cloud Computing. The methods of cognitive data management in Cloud Computing are aimed to support the processes of protecting data against unauthorised takeover and they serve to enhance the data management processes. The accomplishment of the proposed tasks will be the definition of algorithms for the execution of meaning data interpretation processes in safe Cloud Computing. • We proposed a cognitive methods for data description. • Proposed a techniques for secure data in Cloud Computing. • Application of cognitive approaches for medicine was described.

  19. Security model for VM in cloud

    Science.gov (United States)

    Kanaparti, Venkataramana; Naveen K., R.; Rajani, S.; Padmvathamma, M.; Anitha, C.

    2013-03-01

    Cloud computing is a new approach emerged to meet ever-increasing demand for computing resources and to reduce operational costs and Capital Expenditure for IT services. As this new way of computation allows data and applications to be stored away from own corporate server, it brings more issues in security such as virtualization security, distributed computing, application security, identity management, access control and authentication. Even though Virtualization forms the basis for cloud computing it poses many threats in securing cloud. As most of Security threats lies at Virtualization layer in cloud we proposed this new Security Model for Virtual Machine in Cloud (SMVC) in which every process is authenticated by Trusted-Agent (TA) in Hypervisor as well as in VM. Our proposed model is designed to with-stand attacks by unauthorized process that pose threat to applications related to Data Mining, OLAP systems, Image processing which requires huge resources in cloud deployed on one or more VM's.

  20. Solid-phase extraction in combination with dispersive liquid-liquid microextraction and ultra-high performance liquid chromatography-tandem mass spectrometry analysis: the ultra-trace determination of 10 antibiotics in water samples.

    Science.gov (United States)

    Liang, Ning; Huang, Peiting; Hou, Xiaohong; Li, Zhen; Tao, Lei; Zhao, Longshan

    2016-02-01

    A novel method, solid-phase extraction combined with dispersive liquid-liquid microextraction (SPE-DLLME), was developed for ultra-preconcentration of 10 antibiotics in different environmental water samples prior to ultra-high performance liquid chromatography-tandem mass spectrometry detection. The optimized results were obtained as follows: after being adjusted to pH 4.0, the water sample was firstly passed through PEP-2 column at 10 mL min(-1), and then methanol was used to elute the target analytes for the following steps. Dichloromethane was selected as extraction solvent, and methanol/acetonitrile (1:1, v/v) as dispersive solvent. Under optimal conditions, the calibration curves were linear in the range of 1-1000 ng mL(-1) (sulfamethoxazole, cefuroxime axetil), 5-1000 ng mL(-1) (tinidazole), 10-1000 ng mL(-1) (chloramphenicol), 2-1000 ng mL(-1) (levofloxacin oxytetracycline, doxycycline, tetracycline, and ciprofloxacin) and 1-400 ng mL(-1) (sulfadiazine) with a good precision. The LOD and LOQ of the method were at very low levels, below 1.67 and 5.57 ng mL(-1), respectively. The relative recoveries of the target analytes were in the range from 64.16% to 99.80% with relative standard deviations between 0.7 and 8.4%. The matrix effect of this method showed a great decrease compared with solid-phase extraction and a significant value of enrichment factor (EF) compared with dispersive liquid-liquid microextraction. The developed method was successfully applied to the extraction and analysis of antibiotics in different water samples with satisfactory results.

  1. Effects of water chemistry on flow accelerated corrosion and liquid droplet impingement accelerated corrosion

    International Nuclear Information System (INIS)

    Uchida, Shunsuke; Okada, Hidetoshi; Naitoh, Masanori; Koshizuka, Seiichi; Lister, Derek H.; Svoboda, Robert

    2009-01-01

    Overlapping effects of flow dynamics and corrosion are important issues in determining the reliability and lifetime of major structures and components in light water reactor plants. Flow accelerated corrosion (FAC) and liquid droplet impingement (LDI) accelerated corrosion (LDI (corrosion)) are typical phenomena resulting from both interactions. In order to evaluate local wall thinning due to FAC and LDI (corrosion), a 6-step evaluation procedure for each has been proposed. 1. Obtain the flow pattern along the flow path with a 1D computational flow dynamics (CFD) code. 2. Calculate corrosive conditions, e.g., oxygen concentration along the flow path, with a oxygen-hydrazine reaction code for the FAC evaluation. Calculate the flow pattern of liquid droplets in high velocity steam and determine the possibility of their collision with the pipe inner surface for the LDI (corrosion) evaluation. 3. Calculate the mass transfer coefficients at the structure surface with a 3D CFD code for the FAC evaluation. Calculate the frequency of oxide film rupture due to droplet collision for the LDI (corrosion) evaluation. 4. Evaluate high risk zones for FAC and LDI (corrosion) occurrence by coupling major parameters. 5. Calculate wall thinning rates with the coupled model of static electrochemical analysis and dynamic double oxide layer analysis at the identified high FAC and LDI (corrosion) risk zones. 6. Make a final evaluation of residual life and the effectiveness of countermeasures. It was demonstrated that the calculated FAC rates had good agreement with the measured rates. Further investigation of the accuracy of the LDI (corrosion) evaluation procedures is currently in progress. (orig.)

  2. Liquid Steel at Low Pressure: Experimental Investigation of a Downward Water Air Flow

    Science.gov (United States)

    Thumfart, Maria

    2016-07-01

    In the continuous casting of steel controlling the steel flow rate to the mould is critical because a well-defined flow field at the mould level is essential for a good quality of the cast product. The stopper rod is a commonly used device to control this flow rate. Agglomeration of solid material near the stopper rod can lead to a reduced cross section and thus to a decreased casting speed or even total blockage (“clogging”). The mechanisms causing clogging are still not fully understood. Single phase considerations of the flow in the region of the stopper rod result in a low or even negative pressure at the smallest cross section. This can cause degassing of dissolved gases from the melt, evaporation of alloys and entrainment of air through the porous refractory material. It can be shown that the degassing process in liquid steel is taking place mainly at the stopper rod tip and its surrounding. The steel flow around the stopper rod tip is highly turbulent. In addition refractory material has a low wettability to liquid steel. So the first step to understand the flow situation and transport phenomena which occur near the stopper is to understand the behaviour of this two phase (steel, gas) flow. To simulate the flow situation near the stopper rod tip, water experiments are conducted using a convergent divergent nozzle with three different wall materials and three different contact angles respectively. These experiments show the high impact of the wettability of the wall material on the actual flow structure at a constant gas flow rate.

  3. Electric field measurements in nanosecond pulse discharges in air over liquid water surface

    Science.gov (United States)

    Simeni Simeni, Marien; Baratte, Edmond; Zhang, Cheng; Frederickson, Kraig; Adamovich, Igor V.

    2018-01-01

    Electric field in nanosecond pulse discharges in ambient air is measured by picosecond four-wave mixing, with absolute calibration by a known electrostatic field. The measurements are done in two geometries, (a) the discharge between two parallel cylinder electrodes placed inside quartz tubes, and (b) the discharge between a razor edge electrode and distilled water surface. In the first case, breakdown field exceeds DC breakdown threshold by approximately a factor of four, 140 ± 10 kV cm-1. In the second case, electric field is measured for both positive and negative pulse polarities, with pulse durations of ˜10 ns and ˜100 ns, respectively. In the short duration, positive polarity pulse, breakdown occurs at 85 kV cm-1, after which the electric field decreases over several ns due to charge separation in the plasma, with no field reversal detected when the applied voltage is reduced. In a long duration, negative polarity pulse, breakdown occurs at a lower electric field, 30 kV cm-1, after which the field decays over several tens of ns and reverses direction when the applied voltage is reduced at the end of the pulse. For both pulse polarities, electric field after the pulse decays on a microsecond time scale, due to residual surface charge neutralization by transport of opposite polarity charges from the plasma. Measurements 1 mm away from the discharge center plane, ˜100 μm from the water surface, show that during the voltage rise, horizontal field component (Ex ) lags in time behind the vertical component (Ey ). After breakdown, Ey is reduced to near zero and reverses direction. Further away from the water surface (≈0.9 mm), Ex is much higher compared to Ey during the entire voltage pulse. The results provide insight into air plasma kinetics and charge transport processes near plasma-liquid interface, over a wide range of time scales.

  4. Search for the First-Order Liquid-to-Liquid Phase Transition in Low-Temperature Confined Water by Neutron Scattering

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Sow-Hsin [Massachusetts Institute of Technology (MIT); Wang, Zhe [Massachusetts Institute of Technology (MIT); Kolesnikov, Alexander I [ORNL; Zhang, Yang [ORNL; Liu, Kao-Hsiang [National Taiwan University

    2013-01-01

    It has been conjectured that a 1st order liquid-to-liquid (L-L) phase transition (LLPT) between high density liquid (HDL) and low density liquid (LDL) in supercooled water may exist, as a thermodynamic extension to the liquid phase of the 1st order transition established between the two bulk solid phases of amorphous ice, the high density amorphous ice (HDA) and the low density amorphous ice (LDA). In this paper, we first recall our previous attempts to establish the existence of the 1st order L-L phase transition through the use of two neutron scattering techniques: a constant Q elastic diffraction study of isobaric temperature scan of the D2O density, namely, the equation of state (EOS) measurements. A pronounced density hysteresis phenomenon in the temperature scan of the density above P = 1500 bar is observed which gives a plausible evidence of crossing the 1st order L-L phase transition line above this pressure; an incoherent quasi-elastic scattering measurements of temperature-dependence of the alpha-relaxation time of H2O at a series of pressures, namely, the study of the Fragile-to-Strong dynamic crossover (FSC) phenomenon as a function of pressure which we interpreted as the results of crossing the Widom line in the one-phase region. In this new experiment, we used incoherent inelastic neutron scattering (INS) to measure the density of states (DOS) of H atoms in H2O molecules in confined water as function of temperature and pressure, through which we may be able to follow the emergence of the LDL and HDL phases at supercooled temperature and high pressures. We here report for the first time the differences of librational and translational DOSs between the hypothetical HDL and LDL phases, which are similar to the corresponding differences between the well-established HDA and LDA ices. This is plausible evidence that the HDL and LDL phases are the thermodynamic extensions of the corresponding amorphous solid water HDA and LDA ices.

  5. Determination of polybrominated diphenyl ethers at trace levels in environmental waters using hollow-fiber microporous membrane liquid-liquid extraction and gas chromatography-mass spectrometry.

    Science.gov (United States)

    Fontanals, Núria; Barri, Thaer; Bergström, Staffan; Jönsson, Jan-Ake

    2006-11-10

    In this study, we present a simple and easy-to-use extraction method that is based on a hollow-fiber microporous membrane liquid-liquid extraction (HF-MMLLE), as an extraction technique, followed by gas chromatography-mass spectrometry (GC-MS) to determine a group of brominated flame retardants (BFRs), polybrominated diphenyl ethers (PBDEs), at trace levels in aqueous samples. The hollow-fiber membrane (HF) filled with organic solvent was immersed into the aqueous sample, spiked with the analytes at ng l(-1) level, and stirred for 60 min. The proposed method could attain enrichment factors (E(e)) up to 5200 times, after optimising parameters, such as organic solvent, stirring speed and extraction time, that affect the extraction. The HF-MMLLE-GC-MS method was successfully applied to the extraction of PBDEs from tap, river and leachate water samples with spike recoveries ranging from 85% to 110%. The method validation with reagent and leachate water samples provided good linearity, detection limits of 1.1 ng l(-1) or lower, both in reagent and leachate water, as well as satisfactory precision in terms of repeatability and reproducibility with values of % relative standard deviation (%RSD) lower than 8.6 and 16.9, respectively.

  6. Determination of Wastewater Compounds in Whole Water by Continuous Liquid-Liquid Extraction and Capillary-Column Gas Chromatography/Mass Spectrometry

    Science.gov (United States)

    Zaugg, Steven D.; Smith, Steven G.; Schroeder, Michael P.

    2006-01-01

    A method for the determination of 69 compounds typically found in domestic and industrial wastewater is described. The method was developed in response to increasing concern over the impact of endocrine-disrupting chemicals on aquatic organisms in wastewater. This method also is useful for evaluating the effects of combined sanitary and storm-sewer overflow on the water quality of urban streams. The method focuses on the determination of compounds that are indicators of wastewater or have endocrine-disrupting potential. These compounds include the alkylphenol ethoxylate nonionic surfactants, food additives, fragrances, antioxidants, flame retardants, plasticizers, industrial solvents, disinfectants, fecal sterols, polycyclic aromatic hydrocarbons, and high-use domestic pesticides. Wastewater compounds in whole-water samples were extracted using continuous liquid-liquid extractors and methylene chloride solvent, and then determined by capillary-column gas chromatography/mass spectrometry. Recoveries in reagent-water samples fortified at 0.5 microgram per liter averaged 72 percent ? 8 percent relative standard deviation. The concentration of 21 compounds is always reported as estimated because method recovery was less than 60 percent, variability was greater than 25 percent relative standard deviation, or standard reference compounds were prepared from technical mixtures. Initial method detection limits averaged 0.18 microgram per liter. Samples were preserved by adding 60 grams of sodium chloride and stored at 4 degrees Celsius. The laboratory established a sample holding-time limit prior to sample extraction of 14 days from the date of collection.

  7. On-line micro-volume introduction system developed for lower density than water extraction solvent and dispersive liquid-liquid microextraction coupled with flame atomic absorption spectrometry.

    Science.gov (United States)

    Anthemidis, Aristidis N; Mitani, Constantina; Balkatzopoulou, Paschalia; Tzanavaras, Paraskevas D

    2012-07-06

    A simple and fast preconcentration/separation dispersive liquid-liquid micro extraction (DLLME) method for metal determination based on the use of extraction solvent with lower density than water has been developed. For this purpose a novel micro-volume introduction system was developed enabling the on-line injection of the organic solvent into flame atomic absorption spectrometry (FAAS). The effectiveness and efficiency of the proposed system were demonstrated for lead and copper preconcentration in environmental water samples using di-isobutyl ketone (DBIK) as extraction solvent. Under the optimum conditions the enhancement factor for lead and copper was 187 and 310 respectively. For a sample volume of 10 mL, the detection limit (3 s) and the relative standard deviation were 1.2 μg L(-1) and 3.3% for lead and 0.12 μg L(-1) and 2.9% for copper respectively. The developed method was evaluated by analyzing certified reference material and it was applied successfully to the analysis of environmental water samples. Copyright © 2012 Elsevier B.V. All rights reserved.

  8. Determination of trace mercury in water based on N-octylpyridinium ionic liquids preconcentration and stripping voltammetry.

    Science.gov (United States)

    Li, Zhenhan; Xia, Shanhong; Wang, Jinfen; Bian, Chao; Tong, Jianhua

    2016-01-15

    A novel method for determination of trace mercury in water is developed. The method is performed by extracting mercury firstly with ionic liquids (ILs) and then detecting the concentration of mercury in organic media with anodic stripping voltammetry. Liquid-liquid extraction of mercury(II) ions by four ionic liquids with N-octylpyridinium cations ([OPy](+)) was studied. N-octylpyridinium tetrafluoroborate and N-octylpyridinium trifluoromethylsulfonate were found to be efficient and selective extractant for mercury. Temperature controlled dispersive liquid phase microextraction (TC-DLPME) technique was utilized to improve the performance of preconcentration. After extraction, precipitated IL was diluted by acetonitrile buffer and mercury was detected by differential pulse stripping voltammetry (DPSV) with gold disc electrode. Mercury was enriched by 17 times while interfering ions were reduced by two orders of magnitude in the organic media under optimum condition. Sensitivity and selectivity for electrochemical determination of mercury were improved by using the proposed method. Tap, pond and waste water samples were analyzed with recoveries ranging from 81% to 107% and detection limit of 0.05 μg/L. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. A tale of gastric layering and sieving: Gastric emptying of a liquid meal with water blended in or consumed separately.

    Science.gov (United States)

    Camps, Guido; Mars, Monica; de Graaf, Cees; Smeets, Paul A M

    2017-07-01

    The process of gastric emptying determines how fast gastric content is delivered to the small intestine. It has been shown that solids empty slower than liquids and that a blended soup empties slower than the same soup as broth and chunks, due to the liquid fraction emptying more quickly. This process of 'gastric sieving' has not been investigated for liquid foods. To determine whether gastric sieving of water can also occur for liquid foods. Two groups of men participated in a parallel design (n=15, age 22.6±2.4y, BMI 22.6±1.8kg/m 2 , and n=19, age 22.2±2.5y, BMI 21.8±1.5kg/m 2 ) and consumed an isocaloric shake (2093kJ, CARBOHYDRATES: 71g, FAT: 18g, PROTEIN: 34g), either in a 500-mL version (MIXED) or as a 150-mL shake followed by 350mL water (SEPARATE). Participants provided appetite ratings and were scanned using MRI to determine gastric emptying rate and volume at three time-points within 35min post ingestion. Gastric emptying the percentage emptied in 35min was significantly smaller for MIXED (29±19%) than for SEPARATE (57±11%, psieving can occur for liquid foods; water is able to drain from the stomach while a layer of nutrient rich liquid is retained. In indirect gastric emptying measurements, the behavior of labelling agents may be affected by the layering and confound emptying measurements. Copyright © 2017 Elsevier Inc. All rights reserved.

  10. Separation of americium by liquid-liquid extraction using diglycol-amides water-soluble complexing agents

    Energy Technology Data Exchange (ETDEWEB)

    Chapron, S.; Marie, C.; Pacary, V.; Duchesne, M.T.; Miguirditchian, M. [CEA, Centre de Marcoule, Nuclear Energy Division, RadioChemistry and Processses Departement, 30207 Bagnols-sur-Ceze (France); Arrachart, G.; Pellet-Rostaing, S. [Institut de Chimie Separative de Marcoule, LTSM, Bat 426, F-30207 Bagnols-sur- Ceze (France)

    2016-07-01

    Recycling americium (Am) alone from spent nuclear fuels is an important option studied for the future nuclear cycle (Generation IV systems) since Am belongs to the main contributors of the long-term radiotoxicity and heat power of final waste. Since 2008, a liquid-liquid extraction process called EXAm has been developed by the CEA to allow the recovery of Am alone from a PUREX raffinate (a dissolution solution already cleared from U, Np and Pu). A mixture of DMDOHEMA (N,N'-dimethyl-N,N'-dioctyl-2-(2-(hexyloxy)ethyl)-malonamide) and HDEHP (di-2-ethylhexylphosphoric acid) in TPH is used as the solvent and the Am/Cm selectivity is improved using TEDGA (N,N,N',N'-tetraethyl-diglycolamide) as a selective complexing agent to maintain Cm and heavier lanthanides in the acidic aqueous phase (5 M HNO{sub 3}). Americium is then stripped selectively from light lanthanides at low acidity (pH=3) with a poly-aminocarboxylic acid. The feasibility of sole Am recovery was already demonstrated during hot tests in ATALANTE facility and the EXAm process was adapted to a concentrated raffinate to optimize the process compactness. The speciation of TEDGA complexes formed in the aqueous phase with Am, Cm and lanthanides was studied to better understand and model the behavior of TEDGA in the process. Some Ln-TEDGA species are extracted into the organic phase and this specific chemistry might play a role in the Am/Cm selectivity improvement. Hence the hydrophilicity-lipophilicity balance of the complexing agent is an important parameter. In this comprehensive study, new analogues of TEDGA were synthesized and tested in the EXAm process conditions to understand the relationship between their structure and selectivity. New derivatives of TEDGA with different N-alkyl chain lengths and ramifications were synthesized. The impact of lipophilicity on ligand partitioning and Am/Cm selectivity was investigated. (authors)

  11. A fractal model for predicting permeability and liquid water relative permeability in the gas diffusion layer (GDL) of PEMFCs

    Science.gov (United States)

    He, Guangli; Zhao, Zongchang; Ming, Pingwen; Abuliti, Abudula; Yin, Caoyong

    In this study, a fractal model is developed to predict the permeability and liquid water relative permeability of the GDL (TGP-H-120 carbon paper) in proton exchange membrane fuel cells (PEMFCs), based on the micrographs (by SEM, i.e. scanning electron microscope) of the TGP-H-120. Pore size distribution (PSD), maximum pore size, porosity, diameter of the carbon fiber, pore tortuosity, area dimension, hydrophilicity or hydrophobicity, the thickness of GDL and saturation are involved in this model. The model was validated by comparison between the predicted results and experimental data. The results indicate that the water relative permeability in the hydrophobicity case is much higher than in the hydrophilicity case. So, a hydrophobic carbon paper is preferred for efficient removal of liquid water from the cathode of PEMFCs.

  12. Isomerization reaction dynamics and equilibrium at the liquid-vapor interface of water. A molecular-dynamics study

    Science.gov (United States)

    Benjamin, Ilan; Pohorille, Andrew

    1993-01-01

    The gauche-trans isomerization reaction of 1,2-dichloroethane at the liquid-vapor interface of water is studied using molecular-dynamics computer simulations. The solvent bulk and surface effects on the torsional potential of mean force and on barrier recrossing dynamics are computed. The isomerization reaction involves a large change in the electric dipole moment, and as a result the trans/gauche ratio is considerably affected by the transition from the bulk solvent to the surface. Reactive flux correlation function calculations of the reaction rate reveal that deviation from the transition-state theory due to barrier recrossing is greater at the surface than in the bulk water. This suggests that the system exhibits non-Rice-Ramsperger-Kassel-Marcus behavior due to the weak solvent-solute coupling at the water liquid-vapor interface.

  13. Determining the level of gross alpha and beta radioactivity of water from Marilao river using liquid scintillation counter

    International Nuclear Information System (INIS)

    Cruz, J.; Magtaka, J.; Balisi, R.; Castaneda, Soledad; De Vero, J.

    2009-01-01

    This study aims to determine the level of gross alpha- and beta- radioactivity present in the Marilao River. Liquid Scintillation Counter was used to detect samples radioactivity. Water samples were taken along the different spots of Marilao River. The results showed that the radioactivity are below the Philippine National Standard for Drinking Water (PNSDW) which is 0.1 Bq/L for gross alpha activity and 1.0 Bq/L for gross beta activity set by the Dept. of Health. Hence water samples from Marilao River, is safe in terms of the level of radioactivity levels.(author)

  14. Determination of seven pyrethroids and six pyrethrins in water by liquid chromatography/mass spectrometry

    Science.gov (United States)

    ccanccapa, alexander; Masia, Ana; Pico, Yolanda

    2016-04-01

    Pyrethroids are the synthetic analogues of pyrethrins which were developed as pesticides from the extracts of dried and powdered flower heads of Chrysanthemum cinerariaefolium. They are increasingly used in agriculture due to their broad biological activity and slow development of pest resistance. Contamination of fresh-water ecosystems appears either because of the direct discharge of industrial and agricultural effluents or as a result of effluents from sewage treatment works; residues can thus accumulate in the surrounding biosphere [1, 2]. These substances, mostly determined by gas chromatography mass spectrometry (GC-MS) can be difficult to analyse due to their volatility and degradability. The purpose of this study is, as an alternative, to develop a fast and sensitive multi-residue method for the target analysis of 7 pyrethroids and the 6 natural pyrethrins currently used in water samples by liquid chromatography tandem mass spectrometry (LC-MS/MS). The compounds included in the study were acrinathrin, etofenprox, cyfluthrin, esfenvalerate, cyhalothrin, cypermethrin and flumethrin as pyrethroids and a commercial mix of pyrethrins containing Cinerin I, Jasmolin I, pyrethrin I, cinerin II, jasmolin II, pyrethrins II in different percentages. As a preliminary step, the ionization and fragmentation of the compounds were optimized injecting individual solutions of each analyte at 10 ppm in the system, using a gradient elution profile of water-methanol both with 10 mM ammonium formate. The ESI conditions were: capillary voltage 4000 V, nebulizer15 psi, source temperature 300◦C and gas flow 10 L min-1. [M+H]+, [M+Na]+ ,[M+NH3]+ ,[M+NH4+]+ were tested as precursor ions. The most intense signal was for ammonium adduct for all compounds. The optimal fragmentor range for product ions were between 20 to 80 ev and the collision energy ranged between 5 to 86 ev. The efficiency of the method was tested in water samples from Turia River without any known exposure to

  15. Interaction of water vapor with the surfaces of imidazolium-based ionic liquid nanoparticles and thin films.

    Science.gov (United States)

    MacMillan, Amanda C; McIntire, Theresa M; Freites, J Alfredo; Tobias, Douglas J; Nizkorodov, Sergey A

    2012-09-13

    Understanding the interactions of humid air with ionic liquids (ILs) is critical for predicting how their physicochemical properties are affected by water. Using experimental and theoretical techniques, water vapor's interaction with aerosolized nanoparticles and thin films of [C(2)MIM][Cl] and [C(2)MIM][BF(4)] was studied. Solutions were electrosprayed to produce dry particles. Particles' hygroscopic growth was quantified using tandem nanodifferential mobility analysis as a function of relative humidity (RH). This is the first report of the interaction of water with aerosolized IL nanoparticles. The particles' small size allows true IL-water vapor equilibrium achieved quickly. Growth curves for both ILs show steady water uptake with increasing RH. Water vapor uptake by IL thin films was also examined using ATR-FTIR spectroscopy. Both experimental methods show [C(2)MIM][Cl] absorbs more water vapor than [C(2)MIM][BF(4)] over the entire RH range. Water molar fractions, calculated from growth curves, agreed well with those estimated from ATR-FTIR data. MD simulations, used to model IL-water interactions, revealed strong interactions between [Cl(-)] and water and considerably weaker interactions between [BF(4)(-)] and water. Widths and position of O-H stretching vibrations from MD simulations qualitatively reproduced ATR-FTIR results. These experimental and theoretical data provide a comprehensive picture of the behavior of absorbed water in ILs.

  16. Lignin monomer composition affects Arabidopsis cell-wall degradability after liquid hot water pretreatment

    Directory of Open Access Journals (Sweden)

    Ladisch Michael

    2010-12-01

    Full Text Available Abstract Background Lignin is embedded in the plant cell wall matrix, and impedes the enzymatic saccharification of lignocellulosic feedstocks. To investigate whether enzymatic digestibility of cell wall materials can be improved by altering the relative abundance of the two major lignin monomers, guaiacyl (G and syringyl (S subunits, we compared the degradability of cell wall material from wild-type Arabidopsis thaliana with a mutant line and a genetically modified line, the lignins of which are enriched in G and S subunits, respectively. Results Arabidopsis tissue containing G- and S-rich lignins had the same saccharification performance as the wild type when subjected to enzyme hydrolysis without pretreatment. After a 24-hour incubation period, less than 30% of the total glucan was hydrolyzed. By contrast, when liquid hot water (LHW pretreatment was included before enzyme hydrolysis, the S-lignin-rich tissue gave a much higher glucose yield than either the wild-type or G-lignin-rich tissue. Applying a hot-water washing step after the pretreatment did not lead to a further increase in final glucose yield, but the initial hydrolytic rate was doubled. Conclusions Our analyses using the model plant A. thaliana revealed that lignin composition affects the enzymatic digestibility of LHW pretreated plant material. Pretreatment is more effective in enhancing the saccharification of A. thaliana cell walls that contain S-rich lignin. Increasing lignin S monomer content through genetic engineering may be a promising approach to increase the efficiency and reduce the cost of biomass to biofuel conversion.

  17. Varying the charge of small cations in liquid water: Structural, transport, and thermodynamical properties

    Science.gov (United States)

    Martelli, Fausto; Vuilleumier, Rodolphe; Simonin, Jean-Pierre; Spezia, Riccardo

    2012-10-01

    In this work, we show how increasing the charge of small cations affects the structural, thermodynamical, and dynamical properties of these ions in liquid water. We have studied the case of lanthanoid and actinoid ions, for which we have recently developed accurate polarizable force fields, and the ionic radius is in the 0.995-1.250 Å range, and explored the valency range from 0 to 4+. We found that the ion charge strongly structures the neighboring water molecules and that, in this range of charges, the hydration enthalpies exhibit a quadratic dependence with respect to the charge, in line with the Born model. The diffusion process follows two main regimes: a hydrodynamical regime for neutral or low charges, and a dielectric friction regime for high charges in which the contraction of the ionic radius along the series of elements causes a decrease of the diffusion coefficient. This latter behavior can be qualitatively described by theoretical models, such as the Zwanzig and the solvated ion models. However, these models need be modified in order to obtain agreement with the observed behavior in the full charge range. We have thus modified the solvated ion model by introducing a dependence of the bare ion radius as a function of the ionic charge. Besides agreement between theory and simulation this modification allows one to obtain an empirical unified model. Thus, by analyzing the contributions to the drag coefficient from the viscous and the dielectric terms, we are able to explain the transition from a regime in which the effect of viscosity dominates to one in which dielectric friction governs the motion of ions with radii of ca. 1 Å.

  18. Repeatability of n-octanol/water partition coefficient values between liquid chromatography measurement methods.

    Science.gov (United States)

    Saranjampour, Parichehr; Armbrust, Kevin

    2018-03-20

    The n-octanol/water partition coefficient (K OW ) is a physical/chemical property that is extensively used for regulatory and environmental risk and exposure assessments. The K OW value can estimate various chemical properties such as water solubility, bioavailability, and toxicity using quantitative structure-activity relationships which demands an accurate knowledge of this property. The present investigation aims to compare outcomes of three commonly cited methods of K OW measurement in the literature for six hydrophobic chemicals with insecticidal functions as well as highly volatile petroleum constituents. This measurement has been difficult to obtain for the selected pyrethroid insecticides, cypermethrin, and bifenthrin and is a novel measurement for the latter: polycyclic aromatic sulfur heterocycles, dibenzothiophene (DBT), and three of its alkyl derivatives except for DBT. The K OW values were obtained using two liquid chromatographic methods with isocratic and gradient programming, and the slow-stirring method following OECD 117 and 123 guidelines, respectively. The mean log K OW values of bifenthrin, cypermethrin, DBT, methyl-DBT, dimethyl-DBT, and diethyl-DBT were 8.4 ± 0.1, 6.0 ± 0.3, 4.8 ± 0.0, 5.4 ± 0.1, 6.0 ± 0.1, and 6.8 ± 0.0 using the HPLC method with gradient programing. The K OW values were significantly reproducible within a method, however, not between the methods. Results suggest assessing a chemical's property and environmental risk and exposure solely based on the K OW value should be practiced with caution.

  19. PDF Estimation and Liquid Water Content Based Attenuation Modeling for Fog in Terrestrial FSO Links

    Directory of Open Access Journals (Sweden)

    S. S. Muhammad

    2010-06-01

    Full Text Available Terrestrial Free-space optical communication (FSO links have yet to achieve a mass market success due to the ever elusive 99.999% availability requirement. The terrestrial FSO links are heavily affected by atmospheric fog. To design systems which can achieve high availability and reliability in the presence of fog, accurate and better models of fog attenuation need to be developed. The current article puts forth appropriate probability density function estimates for received signal strength (hereafter RSS under fog conditions, where variations in the RSS during foggy events have been statistically characterized. Moreover, from the surface observations of fog density, liquid water content (hereafter LWC of fog is estimated. The actual measured optical attenuations are then compared with the optical attenuations estimated from LWC. The results presented suggest that fog density measurements carried out are accurate representation of the fog intensity and the attenuation predictions obtained by the LWC estimate match the actual measured optical attenuations. This suggests that the LWC is a useful parameter besides visibility range to predict optical attenuations in the presence of hydrometeors.

  20. A GC-TCD method for measuring the liquid water mass of collected aerosols

    Science.gov (United States)

    Lee, Chung-Te; Chang, Shih-Yu

    This work presents a gas chromatographic method that uses a thermal conductivity detector (GC-TCD) to measure the liquid water mass (LWM) of collected aerosols. The method is a modification of the previously developed EA-TCD method (Journal of Aerosol Science 29, 827). A microcomputer was incorporated into the system to control the analytical procedures, improve the measurement precision, and make possible a continuous operation. To validate the method, the aerosol LWMs of NaCl, Na 2SO 4, NH 4NO 3, (NH 4) 2SO 4, NH 4Cl, and Na 2CO 3 were measured at room temperature under relative humidities (RHs) varying between 20% and 90%, in both humidifying and dehumidifying conditions. Estimates of aerosol LWMs for varying aerosol chemical compositions and RHs by various measurement methods and predictive models are comprehensively compared. The comparison shows that the GC-TCD measurements agree closely with those of the other methods. The GC-TCD measurements are closer to the ISORROPIA model predictions than those of the AIM2 model. Most notably, our method determines, for the first time, the hygroscopic behavior of Na 2CO 3 aerosol yielding the deliquescence relative humidity and crystallization relative humidity at 78% and 39% RH, respectively. The hygroscopic characteristics of various NaCl mole fractions in mixed NaCl-Na 2SO 4 aerosols, determined by GC-TCD, are used to show the discrepancy between the measurements and the model's prediction.

  1. Micellar Liquid Chromatographic Determination of Carbaryl and 1-Naphthol in Water, Soil, and Vegetables

    Directory of Open Access Journals (Sweden)

    Mei-Liang Chin-Chen

    2012-01-01

    Full Text Available A liquid chromatographic procedure has been developed for the determination of carbaryl, a phenyl-N-methylcarbamate, and its main metabolite 1-naphthol, using a C18 column (250’mm’ × ’4.6’mm with a micellar mobile phase and fluorescence detection at maximum excitation/emission wavelengths of 225/333’nm, respectively. In the optimization step, surfactants sodium dodecyl sulphate (SDS, Brij-35 and N-cetylpyridinium chloride monohydrate, and organic solvents propanol, butanol, and pentanol were considered. The selected mobile phase was 0.15’M SDS-6% (v/v-pentanol-0.01’M NaH2PO4 buffered at pH 3. Validation studies, according to the ICH Tripartite Guideline, included linearity (r>0.999, limit of detection (5 and 18’ng mL-1, for carbaryl and 1-naphthol, resp., and limit of quantification (15 and 50’ng mL-1, for carbaryl and 1-naphthol, resp., with intra- and interday precisions below 1%, and robustness parameters below 3%. The results show that the procedure was adequate for the routine analysis of these two compounds in water, soil, and vegetables samples.

  2. The calculation of proton and secondary electron stopping powers in liquid water

    International Nuclear Information System (INIS)

    Marouane, Abdelhak; Inchaouh, Jamal; Ouaskit, Said; Fathi, Ahmed

    2012-01-01

    The stopping power of energetic protons in liquid water has been calculated using a new model based on different theoretical and semi-empirical approaches. In this model, we consider the relativistic corrections along with the electronic and nuclear stopping power. The present work accounts for the different interactions made with electrons and nuclei inside the target. Interactions of the incident particle with the target's electrons dominate in the high energy regime; in the low energy regime, the interactions of the projectile with the target nuclei contribute importantly and are included in the calculation. We also compute the stopping cross sections and the stopping power of secondary electrons ejected from proton and hydrogen ionization impact, and generated by hydrogen electron loss processes. The consideration of secondary electrons' stopping power can contribute to the study of nano-dosimetry. Our results are in good agreement with existing experimental data. This calculation model can be useful for different applications in medical physics and space radiation health, such as hadron therapy for cancer treatment or radiation protection for astronauts. - Highlights: ► We discussed the stopping cross sections at the Bragg peak region of primary and secondary processes. ► We considered the corrections of incident particle energy focusing on the Rudds semi-empirical model. ► We calculated the electronic and nuclear stopping power, and we deduced the total stopping power. ► We calculated the stopping power of the secondary electrons.

  3. Measurement of the Spectral Absorption of Liquid Water in Melting Snow With an Imaging Spectrometer

    Science.gov (United States)

    Green, Robert O.; Dozier, Jeff

    1995-01-01

    Melting of the snowpack is a critical parameter that drives aspects of the hydrology in regions of the Earth where snow accumulates seasonally. New techniques for measurement of snow melt over regional scales offer the potential to improve monitoring and modeling of snow-driven hydrological processes. In this paper we present the results of measuring the spectral absorption of liquid water in a melting snowpack with the Airborne Visible/Infrared Imaging Spectrometer (AVIRIS). AVIRIS data were acquired over Mammoth Mountain, in east central California on 21 May 1994 at 18:35 UTC. The air temperature at 2926 m on Mammoth Mountain at site A was measured at 15-minute intervals during the day preceding the AVIRIS data acquisition. At this elevation. the air temperature did not drop below freezing the night of the May 20 and had risen to 6 degrees Celsius by the time of the overflight on May 21. These temperature conditions support the presence of melting snow at the surface as the AVIRIS data were acquired.

  4. Microdosimetry of electrons in liquid water using the low-energy models of Geant4

    Science.gov (United States)

    Kyriakou, I.; Emfietzoglou, D.; Ivanchenko, V.; Bordage, M. C.; Guatelli, S.; Lazarakis, P.; Tran, H. N.; Incerti, S.

    2017-07-01

    The biological effects of ionizing radiation at the cellular level are frequently studied using the well-known formalism of microdosimetry, which provides a quantitative description of the stochastic aspects of energy deposition in irradiated media. Energy deposition can be simulated using Monte Carlo codes, some adopting a computationally efficient condensed-history approach, while others follow a more detailed track-structure approach. In this work, we present the simulation of microdosimetry spectra and related quantities (frequency-mean and dose-mean lineal energies) for incident monoenergetic electrons (50 eV-10 keV) in spheres of liquid water with dimensions comparable to the size of biological targets: base pairs (2 nm diameter), nucleosomes (10 nm), chromatin fibres (30 nm) and chromosomes (300 nm). Simulations are performed using the condensed-history low-energy physics models ("Livermore" and "Penelope") and the track-structure Geant4-DNA physics models, available in the Geant4 Monte Carlo simulation toolkit. The spectra are compared and the influence of simulation parameters and different physics models, with emphasis on recent developments, is discussed, underlining the suitability of Geant4-DNA models for microdosimetry simulations. It is further shown that with an appropriate choice of simulation parameters, condensed-history transport may yield reasonable results for sphere sizes as small as a few tens of a nanometer.

  5. Implementation of new physics models for low energy electrons in liquid water in Geant4-DNA.

    Science.gov (United States)

    Bordage, M C; Bordes, J; Edel, S; Terrissol, M; Franceries, X; Bardiès, M; Lampe, N; Incerti, S

    2016-12-01

    A new alternative set of elastic and inelastic cross sections has been added to the very low energy extension of the Geant4 Monte Carlo simulation toolkit, Geant4-DNA, for the simulation of electron interactions in liquid water. These cross sections have been obtained from the CPA100 Monte Carlo track structure code, which has been a reference in the microdosimetry community for many years. They are compared to the default Geant4-DNA cross sections and show better agreement with published data. In order to verify the correct implementation of the CPA100 cross section models in Geant4-DNA, simulations of the number of interactions and ranges were performed using Geant4-DNA with this new set of models, and the results were compared with corresponding results from the original CPA100 code. Good agreement is observed between the implementations, with relative differences lower than 1% regardless of the incident electron energy. Useful quantities related to the deposited energy at the scale of the cell or the organ of interest for internal dosimetry, like dose point kernels, are also calculated using these new physics models. They are compared with results obtained using the well-known Penelope Monte Carlo code. Copyright © 2016 Associazione Italiana di Fisica Medica. Published by Elsevier Ltd. All rights reserved.

  6. Approximating Matsubara dynamics using the planetary model: Tests on liquid water and ice

    Science.gov (United States)

    Willatt, Michael J.; Ceriotti, Michele; Althorpe, Stuart C.

    2018-03-01

    Matsubara dynamics is the quantum-Boltzmann-conserving classical dynamics which remains when real-time coherences are taken out of the exact quantum Liouvillian [T. J. H. Hele et al., J. Chem. Phys. 142, 134103 (2015)]; because of a phase-term, it cannot be used as a practical method without further approximation. Recently, Smith et al. [J. Chem. Phys. 142, 244112 (2015)] developed a "planetary" model dynamics which conserves the Feynman-Kleinert (FK) approximation to the quantum-Boltzmann distribution. Here, we show that for moderately anharmonic potentials, the planetary dynamics gives a good approximation to Matsubara trajectories on the FK potential surface by decoupling the centroid trajectory from the locally harmonic Matsubara fluctuations, which reduce to a single phase-less fluctuation particle (the "planet"). We also show that the FK effective frequency can be approximated by a direct integral over these fluctuations, obviating the need to solve iterative equations. This modification, together with use of thermostatted ring-polymer molecular dynamics, allows us to test the planetary model on water (gas-phase, liquid, and ice) using the q-TIP4P/F potential surface. The "planetary" fluctuations give a poor approximation to the rotational/librational bands in the infrared spectrum, but a good approximation to the bend and stretch bands, where the fluctuation lineshape is found to be motionally narrowed by the vibrations of the centroid.

  7. Measurements of nanomaterials in environmentally relevant water matrices using liquid nebulization/differential mobility analysis.

    Science.gov (United States)

    Mader, Brian T; Ellefson, Mark E; Wolf, Susan T

    2015-04-01

    A liquid nebulization-differential mobility analysis methodology was evaluated for the measurement of the size distribution and quantitative mass concentration of nanomaterials in environmentally relevant aqueous media. The analysis time is 8 min, and the method requires little routine sample preparation and less than 8 mL of sample. The method can be used for rapid, direct analysis of nanomaterials in aqueous media with a particular application to dose verification in ecotoxicology studies, analysis of manufacturing process waste streams, and raw material analysis. Twelve reference materials having a diameter traceable to the National Institute of Standards and Technology were spiked into 6 different aqueous matrices that included drinking water, groundwater, industrial wastewater, as well as the algae and daphnia media used in ecotoxicology testing. Measurement of the diameter of a reference material was within the expected range for the reference material. Individual response factors for each reference material were determined in each medium and the accuracy and precision of the concentration measurements evaluated. In ecotoxicology test media, measurements of the concentration of nanoparticles having diameter ≥ 30 nm, had corresponding accuracies and precisions of 103% and 7%, respectively. Over 28 d 86% of the samples had concentrations within 20% of the initial concentration. The method limit of quantification depended primarily on matrix complexity and particle diameter; the limit of quantification ranged from 0.01 mg/L to 3 g/L. © 2014 SETAC.

  8. Energy Efficiency in Cloud Software Architectures

    NARCIS (Netherlands)

    Procaccianti, G.; Bevini, S.; Lago, P.; Bernd Page, B. P.; Andreas G. Fleischer, A. G. F.; Johannes Gobel, J. G.; Volker Wohlgemuth, V. W.

    2013-01-01

    Cloud-based software is often considered as providing a greener, more energy-efficient solution. At the same time, it introduces more complexity and demands for new investments in cloud services, technologies, and competencies for migration, maintenance, and evolution of the underlying software

  9. Investigation of liquid water in gas diffusion layers of polymer electrolyte fuel cells using X-ray tomographic microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Flueckiger, Reto [Electrochemistry Laboratory, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Marone, Federica [Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Stampanoni, Marco [Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Institute for Biomedical Engineering, University and ETH Zurich, Gloriastrasse 35, CH-8092 Zurich (Switzerland); Wokaun, Alexander [Electrochemistry Laboratory, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Buechi, Felix N., E-mail: felix.buechi@psi.c [Electrochemistry Laboratory, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland)

    2011-02-01

    In polymer electrolyte fuel cells (PEFCs), condensation of water within the pore network of the gas diffusion layers (GDL) can influence the gas transport properties and thus reduce the electrochemical conversion rates. The use of X-ray tomographic microscopy (XTM), which allows for a resolution in the order of one micrometer is investigated for studying ex situ the local saturation in GDL's. The strength of XTM is the high spatial resolution with simultaneous contrast for water and carbon, allowing for non-destructive 3D-imaging of the solid and the contained water. The application of this method for imaging the ex situ water intrusion into the porous network of GDLs is explored using absorption and phase contrast methods. It is shown that the inhomogeneous filling behavior of GDL materials can indeed be visualized with sufficient resolution. For Toray paper TGP-H-060 the local saturation was measured as function of the water pressure. The results, evaluated in 1D, 2D and 3D show a liquid water retention effect at the denser layers near the surface. A comparison with established capillary pressure functions is presented. Altogether, the results show the potential of the XTM-method as a tool for studying the liquid water behavior in PEFC on a microscopic scale.

  10. Investigation of liquid water in gas diffusion layers of polymer electrolyte fuel cells using X-ray tomographic microscopy

    International Nuclear Information System (INIS)

    Flueckiger, Reto; Marone, Federica; Stampanoni, Marco; Wokaun, Alexander; Buechi, Felix N.

    2011-01-01

    In polymer electrolyte fuel cells (PEFCs), condensation of water within the pore network of the gas diffusion layers (GDL) can influence the gas transport properties and thus reduce the electrochemical conversion rates. The use of X-ray tomographic microscopy (XTM), which allows for a resolution in the order of one micrometer is investigated for studying ex situ the local saturation in GDL's. The strength of XTM is the high spatial resolution with simultaneous contrast for water and carbon, allowing for non-destructive 3D-imaging of the solid and the contained water. The application of this method for imaging the ex situ water intrusion into the porous network of GDLs is explored using absorption and phase contrast methods. It is shown that the inhomogeneous filling behavior of GDL materials can indeed be visualized with sufficient resolution. For Toray paper TGP-H-060 the local saturation was measured as function of the water pressure. The results, evaluated in 1D, 2D and 3D show a liquid water retention effect at the denser layers near the surface. A comparison with established capillary pressure functions is presented. Altogether, the results show the potential of the XTM-method as a tool for studying the liquid water behavior in PEFC on a microscopic scale.

  11. The Hydrated Electron at the Surface of Neat Liquid Water Appears To Be Indistinguishable from the Bulk Species.

    Science.gov (United States)

    Coons, Marc P; You, Zhi-Qiang; Herbert, John M

    2016-08-31

    Experiments have suggested that the aqueous electron, e(-)(aq), may play a significant role in the radiation chemistry of DNA. A recent measurement of the energy (below vacuum level) of the putative "interfacial" hydrated electron at the water/vacuum interface, performed using liquid microjet photoelectron spectroscopy, has been interpreted to suggest that aqueous electrons at the water/biomolecule interface may possess the appropriate energetics to induce DNA strand breaks, whereas e(-)(aq) in bulk water lies too far below the vacuum level to induce such reactions. Other such experiments, however, find no evidence of a long-lived feature at low binding energy. We employ a variety of computational strategies to demonstrate that the energetics of the hydrated electron at the surface of neat liquid water are not significantly different from those of e(-)(aq) in bulk water and as such are incompatible with dissociative electron attachment reactions in DNA. We furthermore suggest that no stable interfacial species may exist at all, consistent with the interpretation of certain surface-sensitive spectroscopy measurements, and that even if a short-lived, metastable species does exist at the vacuum/water interface, it would be extremely difficult to distinguish, experimentally, from e(-)(aq) in bulk water, using either optical absorption or photoelectron spectroscopy.

  12. [Determination of seven phenoxyacid herbicides in environmental water by high performance liquid chromatography coupled with three phase hollow fiber liquid phase microextraction].

    Science.gov (United States)

    Peng, Xiaojun; Pang, Jinshan; Deng, Aihua

    2011-12-01

    A novel method for the simultaneous determination of seven phenoxyacid herbicides such as dicamba, fluroxypyr, 4-chlorophenoxyacetic acid (4-CPA), 2-methyl-4-chlorophenoxyacetic acid (MCPA), 2, 4-dichlorophenoxyacetic acid (2,4-D), 2,4-dichlorophenoxybutyric acid (2,4-DB) and 4-(2-methyl-4-chlorophenoxy) butyric acid (MCPB) in environmental water by three phase hollow fiber liquid phase microextraction (HF-LPME) coupled with high performance liquid chromatography (HPLC) was developed. In order to optimize the experimental conditions, the orthogonal test has been used. The effects of extraction solvent, pH of the donor phase and acceptor phase, extraction time, stirring speed and salt concentration on the detection were investigated. The optimal experimental conditions were as follows: octanol as organic solvent, pH 3 of donor phase, pH 12 of acceptor phase, extraction time of 30 min, stirring speed of 400 r/min. The results showed that the proposed method provided a wide linear range for 7 phenoxyacid herbicides with correlation coefficients of 0.995 3 - 0.998 8. The detection limits ranged from 0.2 to 1.0 microg/L. The enrichment factors were in the range of 76.7 - 121. The recoveries were in the range of 68% - 104% and the relative standard deviations (RSDs) were less than 8.1% for the environmental water samples. The method has the advantages of sensitivity, simplicity, fastness and the use of very small amounts of organic solvent. The method can meet the requirements of the determination of trace phenoxyacid herbicides in the environmental water samples, and the study provided a useful method for the analysis of trace substances in water samples.

  13. Dispersive liquid-liquid microextraction method based on solidification of floating organic droplet for the determination of thiamphenicol and florfenicol in environmental water samples.

    Science.gov (U